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
rs139789014	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092331	CCAAAATGGACTTTC[C/T]TTGCTCCTCTTCCCA	2177
rs139838412	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10079753	AGCTGTCTAGAACGT[C/T]CAGAACTTCAGATGT	2177
rs139915108	in-del	-/G			intron-variant	FANCD2	GRCh38.p7	3:10047309	CTGTAATTTTCTAGA[-/G]TGCAGAAACCACATG	2177
rs139929432	snp	A/G	8.24069e-05	0.00641846	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085921	TTGGAGGAACTACTC[A/G]GGTGAGTCATAACTA	2177
rs139954082	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100763	GAGCTGGAGGACCAT[A/G]GCTTATTTAAAATTA	2177
rs139958117	snp	C/G	0.00318978	0.0398085	intron-variant	FANCD2	GRCh38.p7	3:10042960	TTTTTCTTCCTCAGT[C/G]TTTCAGGAGATTGTC	2177
rs139993010	snp	A/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10058693	ACTCTGTATTCTATT[A/T]CATTGGTCTATACGT	2177
rs140037501	snp	G/T	0.0444908	0.142359	intron-variant	FANCD2	GRCh38.p7	3:10051672	TATTTTTTAGATGAG[G/T]AGGTTTGAGATTGCT	2177
rs140083233	snp	A/T	0.0209421	0.100162	intron-variant	FANCD2	GRCh38.p7	3:10052329	GATTTTAATTTTTTG[A/T]ATTTTAAGGGAAAAA	2177
rs140157000	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10055040	ATTTGTGTTTACCTG[C/T]AGTTTCCTTTCCCTT	2177
rs140203540	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10075363	TAATTTTTTGTACAT[A/T]TTTTATAGAGACAGG	2177
rs140245580	in-del	-/GAT	0.295088	0.245901	intron-variant	FANCD2	GRCh38.p7	3:10071946	TGTACTTTTGGTGCA[-/GAT]GGGGTTTCACCGTGT	2177
rs140253553	snp	C/T	0.00914312	0.0669923	intron-variant	FANCD2	GRCh38.p7	3:10056313	GTTTGAGTCCCTGTT[C/T]TCAGTTTTTTAGGGT	2177
rs140350157	snp	G/T	0.000839886	0.0204753	synonymous-codon	FANCD2	GRCh38.p7	3:10049379	CCCTGTATAGGAAGT[G/T]GTTGGTGCCTTAGTG	2177
rs140351173	snp	C/T	0.00398564	0.0444627	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084486	TTTCTTTGGTAGAGA[C/T]GGGGTTTCGCCATGT	2177
rs140351495	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025425	ACAAGAGCGAAACTC[C/T]GTCTCAAAAATTAAA	2177
rs140384762	snp	A/C	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10029732	TTCAATCCCTAACCC[A/C]CCTTCCACCCTTTCT	2177
rs140452766	snp	A/C	0.0002472	0.0111148	missense	FANCD2	GRCh38.p7	3:10063884	TGCCAACCTGATCCA[A/C]CATGAAAAGCTGGAT	2177
rs140487797	snp	A/G	0.0154538	0.0865337	intron-variant	FANCD2	GRCh38.p7	3:10060075	AGGAGGCTGAGGCAG[A/G]AGAATCGTTTGAACC	2177
rs140509904	snp	C/T	0.00398564	0.0444627	intron-variant	FANCD2	GRCh38.p7	3:10065677	ATGTTAACAAATCAA[C/T]TGTTGCAAAAACTTT	2177
rs140521180	snp	C/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10030217	TTCTCCTGGCTCAGC[C/T]GCCCAAGTAGCTGGG	2177
rs140601588	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10064643	TCCCCATGATGTTGT[A/G]TTTGAAATTGGTTTG	2177
rs140609464	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084757	AAGATGCTTCTAGAG[A/G]AGAAGATCTAGGACG	2177
rs140738485	in-del	-/CCAGATGGTA	0.295599	0.245806	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026744	GGGCTTTTCTGGAAG[-/CCAGATGGTA]TCGCACGTGTTAAAG	2177
rs140957520	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088235	GGGGTTGGGGTGGGA[C/T]GTGTTGAGCCTTAGG	2177
rs140988477	snp	G/T	0.00199481	0.0315187	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092051	GTGGATGCACTGGTT[G/T]CTACATCTAAGGATA	2177
rs141025354	snp	G/T	0.00557542	0.0525036	intron-variant	FANCD2	GRCh38.p7	3:10053570	AAAATTAAAAAAAAT[G/T]TTTTTGTATTCTCAG	2177
rs141084789	snp	C/T	0.00792291	0.0624394	intron-variant	FANCD2	GRCh38.p7	3:10040541	TGGGTTCCTAGGTGA[C/T]TCATTCTAATGCACA	2177
rs141097910	snp	C/G	0.0162398	0.0886349	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097401	GACAGGTACACCCGG[C/G]GGGGCCCAGTTCAGA	2177
rs141141752	snp	A/G	0.000647106	0.0179759	missense	FANCD2	GRCh38.p7	3:10043860	CCTCAGTATCTGAAC[A/G]CAAGGTAATGTTCAT	2177
rs141142140	snp	A/T	0.00716266	0.059414	intron-variant	FANCD2	GRCh38.p7	3:10080112	TAAAGATGGGGTTTC[A/T]CCATGTTGGCCAGGA	2177
rs141156896	snp	A/C	0.000153988	0.00877328	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101258	GTTATGATGACTCTG[A/C]TTAGACCCCAGATAA	2177
rs141200221	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094692	TTCTGTAGGTATACT[C/G]TCAGAAATGATTTTA	2177
rs141205856	snp	C/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10048464	ACACACCACCACGCC[C/T]GGTTAATTTTTTGTA	2177
rs141233997	snp	A/G	0.00318978	0.0398085	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081608	TGTGGGAGTGTTTTT[A/G]TCTGTATTATTTCAT	2177
rs141346605	snp	A/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10042321	AGAATTTAGGCTCTA[A/T]ATGTAAGATAATAGC	2177
rs141357223	snp	A/G	0.0329836	0.124112	intron-variant, downstream-variant-500B	FANCD2, FANCD2OS	GRCh38.p7	3:10099864	GTGGGGCCTCTGTCT[A/G]TAATGCAATTTGAGT	2177
rs141388853	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10054449	TACATGTATATACAT[A/G]TATATATATATATAT	2177
rs141402609	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10071579	TGTTAAGTGAAATAG[A/G]CCAGGCACAACATAT	2177
rs141497282	snp	G/T	0.00755907	0.0610114	intron-variant	FANCD2	GRCh38.p7	3:10062512	CTCCCAAAGTGCTGG[G/T]AGTACAGGCGTGAGC	2177
rs141497505	snp	A/G	0.00358779	0.0422022	intron-variant	FANCD2	GRCh38.p7	3:10057782	TGAATTGGAATTACT[A/G]TTAAAATTAAAAAAA	2177
rs141522584	snp	A/G	1.7098e-05	0.00292381	stop-gained	FANCD2	GRCh38.p7	3:10065969	TTCTTACTCTCAACT[A/G]GTTCCGAGAGGTGAG	2177
rs141561972	snp	A/G	0.0023933	0.0345097	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097188	TGAGATCACATGACC[A/G]CAGGACCGAGGCGAA	2177
rs141566218	snp	A/T	0.000280082	0.0118306	intron-variant	FANCD2	GRCh38.p7	3:10039702	TGTGCTGCAGTTCTA[A/T]TAGTGTCTTCTACTG	2177
rs141630205	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10035361	TGTAGCAGCTTTAGC[A/G]CAGCCCTGTTGCTGT	2177
rs141634477	snp	A/G	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10067659	AAAAATTAGCCAGGC[A/G]TGGTTGTGGGCACCT	2177
rs141740856	snp	C/G	1.64735e-05	0.00286993	missense	FANCD2	GRCh38.p7	3:10042567	TTTTTAGGTTCGCCA[C/G]TTGGTGATGGATAAG	2177
rs141751369	snp	A/G	0.0162398	0.0886349	intron-variant	FANCD2	GRCh38.p7	3:10077140	TGGGCGGCTGAGGTG[A/G]GACCATCACTTGAGT	2177
rs141783465	snp	A/G	1.6473e-05	0.00286988	splice-acceptor-variant	FANCD2	GRCh38.p7	3:10065393	TATTTCTCCTTCTCA[A/G]ATTGGTGTCTCCGCT	2177
rs141824395	snp	A/C/G	0.000790956	0.0198714	synonymous-codon	FANCD2	GRCh38.p7	3:10052455	CTATGTTCTCAGCAC[A/C/G]CTGGCATTTAGCAAA	2177
rs141824868	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085275	GAAGAAAAGAAACCT[A/C]TGAAGACTTCAGGAA	2177
rs141910244	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082817	TCAGTCTTTCCTGCT[A/G]GACTCTGAGCTCCAT	2177
rs141930398	snp	C/T	0.0178098	0.0926698	intron-variant	FANCD2	GRCh38.p7	3:10078649	ATGAGCCACCGCGCC[C/T]GGCCTCATCTTGCTT	2177
rs142043029	snp	A/G	0.00597247	0.0543191	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086876	TAGCGTGGTGCTTGG[A/G]TTTCTCAGCATACAT	2177
rs142081081	in-del	-/TTT			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085384	TTCAATTCTTTTTTC[-/TTT]TTTCTTTCTTTTTTT	2177
rs142103836	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10041067	GGCGTGGTGGTACGC[A/C]CTTATAATTCTAGCT	2177
rs142238966	snp	A/G	3.29451e-05	0.00405851	missense, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10081367	GCTGCTGAGAATCAC[A/G]GTGTAGTTGATGGAC	2177
rs142313698	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095993	TGGACAGTGAATGTT[C/T]AAGGAATTCTCTTAG	2177
rs142321663	snp	C/T	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10060748	ATGCAGGTGTCTACA[C/T]TGCTGTGTCATTCCT	2177
rs142354499	snp	A/C	0.0135859	0.0812918	FANCD2	3	allele_origin=A(germline)/C(germline)	3:10063832	ATTCCTGCAGTGAGC[A/C]GTCTCCTCAGGCCTC	2177
rs142354541	snp	C/T	0.00557542	0.0525036	intron-variant	FANCD2	GRCh38.p7	3:10030670	TTTGGGAGGCCAAGG[C/T]GGGCAGATCACCTGA	2177
rs142354986	snp	C/T	0.0759472	0.179459	intron-variant	FANCD2	GRCh38.p7	3:10070230	CCTCTGCCCGGCAGC[C/T]GCCCCATCTGAGAAG	2177
rs142365855	snp	A/G	1.79619e-05	0.00299677	splice-donor-variant	FANCD2	GRCh38.p7	3:10072982	AGAAAGGAAAAATAG[A/G]TAAGTATGTTCTTTT	2177
rs142378663	snp	A/C/G	1.64735e-05	0.00286993	intron-variant, missense	FANCD2, FANCD2OS	GRCh38.p7	3:10098853	AGTCTGGCACTGATG[A/C/G]TTGCATTTTGTTAAT	2177
rs142460044	snp	A/G	0.00159617	0.0282053	utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101731	TTGTGGACATCATGG[A/G]TTGTCTAACACCATC	2177
rs142482992	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10039096	AGACATTTTTCTTAA[C/T]ATACGTAAGCATGTA	2177
rs142486494	snp	C/G	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10036570	CCTGGTGCAGTGGCT[C/G]ACACCTGTAATCCCA	2177
rs142624538	snp	A/G	0.382887	0.211757	intron-variant	FANCD2	GRCh38.p7	3:10046760	TTTTTAATCTAAAAC[A/G]GAAAGCTTTACAGCT	2177
rs142821565	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10073857	ATCCAGGGAGGGCAA[A/G]TGACTTGCCCAAAGT	2177
rs142881695	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10072676	TTGATCATACTTAAT[A/G]TGATATTTCTGTGTT	2177
rs142887274	in-del	-/C			intron-variant	FANCD2	GRCh38.p7	3:10046914	CTTCCGTATCCTATT[-/C]TTAAGTAGCTTATAA	2177
rs142962966	snp	C/T			intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10099282	ATAGAAGTTCTTACG[C/T]TTTTTTGTGGTACAG	2177
rs143048416	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10076689	CAAGTATCTAGGGCC[A/C]CTGGCATGCCCCACT	2177
rs143133591	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10029320	GCCTGGGTAACATAG[C/T]GAGACTCCATCTCTA	2177
rs143161480	in-del	-/A	0.302435	0.244439	intron-variant	FANCD2	GRCh38.p7	3:10078947	GATTTCGTCTCAAAC[-/A]AAAAAAAAAGTCTAC	2177
rs143230666	snp	C/T	0.0162398	0.0886349	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027483	CAGGCACTTCCCCCA[C/T]CTCTGCTGTCTGATT	2177
rs143239014	snp	G/T	0.00716266	0.059414	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085734	ATTGATGGTACAGAC[G/T]GGAGGCCAGGATCCT	2177
rs143257772	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10054386	GTATATACATATATA[C/T]ATGTATATACGTATA	2177
rs143306443	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10089921	ATCCTTTTGATAATT[C/T]TGTGAGGTTGGTATC	2177
rs143403347	snp	A/G/T	0.000164722	0.00907399	synonymous-codon, missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088465	TTCCCTTGCCAGACA[A/G/T]TTCCTCTGTCGGGTG	2177
rs143427219	snp	A/G	0.00755907	0.0610114	intron-variant	FANCD2	GRCh38.p7	3:10056182	CTGCGCCCGGCCCCC[A/G]TTCTTTGTTTATACC	2177
rs143492081	snp	C/G	0.0023933	0.0345097	intron-variant	FANCD2	GRCh38.p7	3:10059149	CTTCCGAGTAGCCAG[C/G]ACCACAGGCATGCAC	2177
rs143521229	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095837	AGTTTCTGTTACTTA[C/T]TTCCTCCTCTGGTTC	2177
rs143576157	snp	A/G	0.0341408	0.126114	intron-variant	FANCD2	GRCh38.p7	3:10050421	CGAGGTCAGGAGATC[A/G]AGACCATCCTGCCTA	2177
rs143636999	snp	A/G	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10040147	TCACCCCATTCTCCT[A/G]CCTCAGCCTCCCAAG	2177
rs143656049	in-del	-/GGTTT			intron-variant	FANCD2	GRCh38.p7	3:10047160	TGGGCCAGTGGTTTG[-/GGTTT]GGGTTTGGGTTAGGA	2177
rs143664007	snp	A/T	0.29789	0.24537	intron-variant	FANCD2	GRCh38.p7	3:10044652	TTTAAAGATTTTTCT[A/T]TGGTTGGAATCTGTT	2177
rs143701205	snp	A/G/T	0.000148335	0.00861099	missense	FANCD2	GRCh38.p7	3:10052442	TACGAAAACTCTTCT[A/G/T]TGTTCTCAGCACACT	2177
rs143795867	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027021	TGATGATGAGAATAA[C/T]GGTACCCACCTCAAA	2177
rs143820338	snp	C/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10066807	TCGGCTCACTGCAAC[C/T]TCCGCCTCCCAGGTT	2177
rs143849318	snp	G/T	0.00517822	0.0506191	intron-variant	FANCD2	GRCh38.p7	3:10071784	TGTATTTTTGAGATG[G/T]AGTCTCGCTCTGTCA	2177
rs143915539	snp	C/T	0.00318978	0.0398085	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086675	TTGTAGAGATGTTTT[C/T]GACATGTGGCCAGGC	2177
rs143936557	snp	C/T	0.00141552	0.0265661	missense	FANCD2	GRCh38.p7	3:10034732	GCCTGGAGTCTTACA[C/T]TGAGGATGAAGACAG	2177
rs143964628	snp	C/T	0.0150606	0.0854603	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090709	ATGATCCACCCACCT[C/T]GGCCTCCCAAAGTGC	2177
rs144031110	snp	A/T	0.0134861	0.0810011	intron-variant	FANCD2	GRCh38.p7	3:10055043	TGTGTTTACCTGTAG[A/T]TTCCTTTCCCTTCTT	2177
rs144167156	snp	A/C	0.0023933	0.0345097	intron-variant	FANCD2	GRCh38.p7	3:10069296	TATATAAAGATAGGA[A/C]AAAAAATTATTCGGA	2177
rs144167368	snp	C/T	0.0689899	0.172439	intron-variant	FANCD2	GRCh38.p7	3:10046738	AGTAAGTGTCAGAGA[C/T]TATTGATTTTTAATC	2177
rs144258025	in-del	-/TAC	0.28052	0.24813	intron-variant	FANCD2	GRCh38.p7	3:10074916	TCCTTACATTTAGGT[-/TAC]TACTACTACTACTAC	2177
rs144307802	snp	A/G	0.00557542	0.0525036	intron-variant	FANCD2	GRCh38.p7	3:10079883	ACATTAATATATCCC[A/G]TTTCTTGGTTTCTTG	2177
rs144328585	snp	C/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10035032	CTTGCAAAGAGCCAT[C/G]TGCTCATTTCTGTAT	2177
rs144332316	snp	A/G	0.000265002	0.0115078	missense	FANCD2	GRCh38.p7	3:10043509	AATCAAGAAAGCAGC[A/G]GTCAGAGCTGTATTA	2177
rs144365161	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082756	TAACACTCTGGTATC[C/T]GTTCGTGATAAAACT	2177
rs144380282	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10065745	ATTTTAATCAGATCT[C/T]GGCCTTCAAATATGA	2177
rs144431627	snp	C/G	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10065224	AACCTGGGAGGCAGA[C/G]GTTGCAGTGAGCTGA	2177
rs144432252	snp	A/G	0.0138799	0.0821421	intron-variant	FANCD2	GRCh38.p7	3:10045705	CACCCGGGTTCAAGC[A/G]ATTCTCCTGTCTCAG	2177
rs144497173	snp	A/C	0.0158469	0.0875917	intron-variant	FANCD2	GRCh38.p7	3:10047041	CTTTAGGTGATAATT[A/C]CTCTAGAAATGTAAA	2177
rs144575146	in-del	-/G	0.00953873	0.0683987	intron-variant	FANCD2	GRCh38.p7	3:10050254	TAAGGGCCAGATTTT[-/G]GTCACGGGAATGTAG	2177
rs144729861	snp	C/T	0.00318978	0.0398085	intron-variant	FANCD2	GRCh38.p7	3:10039172	ATGCATAGTAGGTGT[C/T]CGGTAAATGTTAATG	2177
rs144742355	snp	G/T	0.000153988	0.00877328	missense	FANCD2	GRCh38.p7	3:10032943	TATCAGGAATTATTC[G/T]TAAAACGGGAGAGAG	2177
rs144788884	snp	A/C	0.00874735	0.0655527	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083205	GCACTCCAACCTGGG[A/C]AACAGAACCAGACCC	2177
rs144891261	snp	C/T	0.00318978	0.0398085	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025247	AGGTGAGAGCCACCA[C/T]GCCTGGCTGTGAACA	2177
rs144926145	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10028735	CAGTAAGTATCTAGT[C/T]ATTTGTTGCTTTATT	2177
rs145000305	snp	C/T	0.00199481	0.0315187	intron-variant	FANCD2	GRCh38.p7	3:10063162	AGTTCAGGCAGGGCA[C/T]GGTGGTTTGCGATTG	2177
rs145051158	snp	C/T	0.0158469	0.0875917	intron-variant	FANCD2	GRCh38.p7	3:10031786	AGAACATAAAAAATT[C/T]GGATTCCTAGGTCCC	2177
rs145067818	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081769	ATTCCAGATTGTTTG[A/G]TGATGAGCTGAACAC	2177
rs145099733	snp	A/C	0.000182482	0.00955027	missense	FANCD2	GRCh38.p7	3:10067303	TGCAAATAATCCTGG[A/C]AAAGTACTTGGCAGG	2177
rs145118615	snp	A/G	0.0119091	0.0762411	intron-variant	FANCD2	GRCh38.p7	3:10080408	TCAGCTAATTTTTGT[A/G]TTTTTTGTAAAGAAG	2177
rs145129959	snp	A/G	0.000773987	0.0196569	missense	FANCD2	GRCh38.p7	3:10047986	TCTCTAGACCAGAGT[A/G]TAATTTCATTTGGCA	2177
rs145138016	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10050038	GATTGGAGGCAAGGC[G/T]GGTAAGACATAGGAC	2177
rs145139945	snp	C/T	0.00119737	0.0244387	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086505	ATCTTCTTTTTTTTT[C/T]CTTTGAGAGAGAGTC	2177
rs145170666	snp	A/G	3.31033e-05	0.00406823	missense	FANCD2	GRCh38.p7	3:10062194	AGAGCCAACCTGAGC[A/G]ATGAGCAGTGCACAC	2177
rs145352481	snp	C/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10041086	ATAATTCTAGCTACT[C/G]AGGAGGCTGAGATGG	2177
rs145393937	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100791	TTATGCAAATTGGGC[C/T]GGGCGCAATGGCTCA	2177
rs145413280	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025880	AGGTACTGTTATTAT[C/T]CCCATTTCACAGAGG	2177
rs145435265	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084495	TAGAGACGGGGTTTC[A/G]CCATGTTGCCCCCAG	2177
rs145458726	snp	C/T	0.0154538	0.0865337	intron-variant	FANCD2	GRCh38.p7	3:10063499	GCATGTAAAGCAATA[C/T]ATTTTTATTTCATTC	2177
rs145483323	in-del	-/AAAA			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027921	AAAAAAAAAAAAAAA[-/AAAA]AAATCACTTCTTTAG	2177
rs145517746	snp	A/C	0.379446	0.213878	intron-variant	FANCD2	GRCh38.p7	3:10046759	ATTTTTAATCTAAAA[A/C]AGAAAGCTTTACAGC	2177
rs145522204	snp	A/G	0.00809717	0.0631112	FANCD2	3	allele_origin=G(germline)/A(germline)	3:10052475	CATTTAGCAAACAGA[A/G]TGAAGCCAGCAGCCA	2177
rs145554460	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10037552	AATAATATTAGTTTA[A/G]TGCTTGCTTTGGCAG	2177
rs145586834	snp	A/G	1.65512e-05	0.00287669	missense	FANCD2	GRCh38.p7	3:10072942	ACACCTCATACTGTT[A/G]CTGCTATTTCAGCAA	2177
rs145604495	snp	A/G	0.0174175	0.0916809	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084097	TGCCCGGGTTCAAGC[A/G]ATTCTTCTGCCTCAG	2177
rs145660865	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084771	GGAGAAGATCTAGGA[C/T]GTCAGATTGTGCTGG	2177
rs145696766	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10050798	TGAGTTTCAAGAGTG[A/G]GGGATTGGCCGGGCA	2177
rs145703665	snp	A/G	0.00676609	0.0577691	intron-variant	FANCD2	GRCh38.p7	3:10066704	GTAATAAGTAAAACT[A/G]GGGTCACAAGCCTAA	2177
rs145746766	in-del	-/TTTTGTTTTTGT	0.294832	0.245947	intron-variant	FANCD2	GRCh38.p7	3:10045164	TCTTTTTTTGTTTTG[-/TTTTGTTTTTGT]TTTTGTTTTTGTTTT	2177
rs145889419	snp	A/G	4.94205e-05	0.0049707	intron-variant, synonymous-codon	FANCD2, FANCD2OS	GRCh38.p7	3:10098896	GTGGAGCAGAACTTT[A/G]CCTACTTATGTTTAT	2177
rs145937759	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10099054	TTGTTATAGAGTTGA[A/C]AATTTTCTGCATTAT	2177
rs145938983	snp	A/G	0.0123036	0.0774623	intron-variant	FANCD2	GRCh38.p7	3:10058647	CCTTGTCAAAAATCA[A/G]TTTGTCACATATATG	2177
rs145953386	snp	A/G	0.0001812	0.00951667	synonymous-codon	FANCD2	GRCh38.p7	3:10078098	TACAGAAGTTGTGCA[A/G]CTTGGGCCCCCTGAG	2177
rs146011215	in-del	-/C			intron-variant	FANCD2	GRCh38.p7	3:10066111	CTCTAGCTGTTATGT[-/C]CCACCACTCCCCAGT	2177
rs146039927	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096563	GTCACCTAAGCCCTC[A/G]TCTCTCAGTAAGGCT	2177
rs146080096	snp	A/C/G	1.64754e-05	0.00287009	intron-variant	FANCD2	GRCh38.p7	3:10078222	GGCAGAAGCATAGGA[A/C/G]TTGGGCATAGTGGAT	2177
rs146098472	snp	A/G	4.94458e-05	0.00497197	missense	FANCD2	GRCh38.p7	3:10046683	GATCAGGCTGCATTC[A/G]AGAACAGCTGCTCCA	2177
rs146277083	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10062599	GAATTGCTTCTAGTC[A/G]CTGTCAGTTCACCAG	2177
rs146306616	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10030725	GCCAACATAGTGAAA[C/T]CCCATCTCTACTAAA	2177
rs146316187	snp	G/T	0.0157612	0.0873623	splice-donor-variant	FANCD2	GRCh38.p7	3:10046724	TCTGTTCATTACTTA[G/T]TAAGTGTCAGAGACT	2177
rs146398232	snp	A/G	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10078996	CTGTAATTCCAGCAC[A/G]TTGGAAGGCCGAGGC	2177
rs146432643	in-del	-/CAAGGGACTAATAACTG	0.0741063	0.177655	intron-variant	FANCD2	GRCh38.p7	3:10069260	AAACTATGTATCTGA[-/CAAGGGACTAATAACTG]CAAGGGACTAATAAC	2177
rs146496253	snp	G/T	0.000230715	0.010738	missense	FANCD2	GRCh38.p7	3:10063897	CAACATGAAAAGCTG[G/T]ATCCAAAAGCCCTGG	2177
rs146509445	snp	C/T	0.000230597	0.0107352	missense	FANCD2	GRCh38.p7	3:10065405	TCAGATTGGTGTCTC[C/T]GCTGTGCCTGGCTCC	2177
rs146685001	in-del	-/G			intron-variant	FANCD2	GRCh38.p7	3:10054265	TTGGAATCATAACTT[-/G]TAACTCGTTTGTAGC	2177
rs146722676	snp	C/T	0.0162398	0.0886349	intron-variant	FANCD2	GRCh38.p7	3:10056212	CACATTTTGTTTATC[C/T]ATTCATCCATTGATG	2177
rs146741161	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10059264	AGCAGTCCAGCAGCC[C/T]CAGCCTCCCAAAGTG	2177
rs146741453	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025286	GATGGCCTACCATGT[A/G]CCTTGCACTCTGCTG	2177
rs146759790	in-del	-/AAC	0.00795532	0.062565	intron-variant	FANCD2	GRCh38.p7	3:10069037	AATTATGAAACTACT[-/AAC]AACAACAACAAAAAA	2177
rs146844942	snp	C/T	0.00755907	0.0610114	intron-variant	FANCD2	GRCh38.p7	3:10071851	TGCGACCTCTGCCTC[C/T]TGGGTTCAAGCAATT	2177
rs146883548	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10045377	GCTTCATCATGTTAG[C/T]CAGGATGGTCTCAAT	2177
rs146905349	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10060781	CGGGAACTTTATACA[C/T]TTGATACAAATAAGA	2177
rs147015204	snp	C/T	1.64765e-05	0.00287019	synonymous-codon	FANCD2	GRCh38.p7	3:10041623	TTCTACCATTCACAG[C/T]GACCTACTGATAGAG	2177
rs147032269	snp	A/G	0.00835141	0.0640778	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097196	CATGACCGCAGGACC[A/G]AGGCGAAATTGAAAT	2177
rs147032689	snp	A/G	0.0240643	0.107019	intron-variant	FANCD2	GRCh38.p7	3:10056994	TGAGTAGCTGGGACC[A/G]TAGGTGTGCACCACC	2177
rs147049272	snp	G/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10060630	TGGTTAAAAATTAAG[G/T]ATTGGCTAGAGGTAA	2177
rs147205530	snp	A/C/G	0.000115331	0.00759304	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094362	GTTTTAGAAAACACC[A/C/G]GGTAAGAGCTAAGAG	2177
rs147264450	in-del	-/AAT	0.293551	0.246177	intron-variant	FANCD2	GRCh38.p7	3:10053537	TATAATAATAATAAA[-/AAT]AAAATAAAATAGAAT	2177
rs147278790	in-del	-/A			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101066	GAGCAAGACTCCTTT[-/A]AAAAAAAAAAAAAGT	2177
rs147294022	snp	C/G	0.0383715	0.133092	intron-variant	FANCD2	GRCh38.p7	3:10055429	GATATGTATCCTTTT[C/G]CGTCTCGCTTATTTC	2177
rs147310128	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10057593	TGATCTCAATCTCTT[A/G]ACCTCATGATCTGCC	2177
rs147327105	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027056	TTTGTGGGAAATAAA[C/T]GAATTATTAAATATA	2177
rs147420181	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10073073	TGGCATCAGTAATTG[G/T]AACAATTGTATAACT	2177
rs147420355	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10042442	GTTTTTCCCTAAATT[A/G]TAAGTGGGAAGATGG	2177
rs147426418	snp	A/G	0.000395491	0.0140566	synonymous-codon	FANCD2	GRCh38.p7	3:10028690	ACTGTCAAAATCTGA[A/G]GATAAAGAGAGCCTG	2177
rs147436881	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10044393	AGATGATTGGCCGGG[C/T]GCGGTAGCTCACGCC	2177
rs147492720	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100719	TATATCGAATGCCCT[C/G]TTTGTTCCTATGTCA	2177
rs147523071	snp	C/T	0.00195405	0.0311963	FANCD2	3	allele_origin=T(germline)/C(germline)	3:10062161	TTTAGAAGTGAATCA[C/T]CTAGTTTGACCCAAG	2177
rs147532349	snp	C/G	4.94368e-05	0.00497152	missense	FANCD2	GRCh38.p7	3:10064823	CCGCTGCTGTTTTCT[C/G]AGGACTTTGCAAAAG	2177
rs147665840	snp	A/G	0.00914312	0.0669923	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100930	AAAAATTAGCCGGGC[A/G]TGGTGGCACATGCCT	2177
rs147675860	snp	C/T	0.00241913	0.0346946	FANCD2, FANCD2OS	3	allele_origin=T(germline)/C(germline)	3:10087244	AATCAACAGCTTCTG[C/T]TCAGAACAAAGAAAA	2177
rs147694705	in-del	-/G			intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10099482	TGAAAAATAAACCTG[-/G]GGTGCGGTGGCTCAC	2177
rs147752638	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097241	TGGGCACCACTGTCA[C/T]TGATAACATCTTATC	2177
rs147806127	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083423	AAGACTTAGCATGCC[A/G]AGTGTTGGTGAGAAG	2177
rs147890891	snp	A/T	0.000807109	0.0200724	intron-variant	FANCD2	GRCh38.p7	3:10039692	TTCTGGGTAATGTGC[A/T]GCAGTTCTAATAGTG	2177
rs147907301	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10042808	CAGATTCATTGATCT[A/G]TATAAGCTGCTATAA	2177
rs148087395	snp	A/C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085225	AACCTATGGCCCAGG[A/C/T]GTGGTGGCTCACCCC	2177
rs148201951	in-del	-/AATC			intron-variant	FANCD2	GRCh38.p7	3:10046849	TTTTGTTTTTGCATT[-/AATC]ATTTTAATTGTCTAT	2177
rs148211192	snp	A/G	0.000153988	0.00877328	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101228	CTGGAGAAAAGGAGC[A/G]AGATAGTGATGAGAG	2177
rs148249750	in-del	-/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092442	GGCATTTTTTTTTTT[-/T]GTCTTTTCCTTCCTT	2177
rs148255762	snp	C/T	8.24002e-05	0.0064182	missense	FANCD2	GRCh38.p7	3:10046680	TTCGATCAGGCTGCA[C/T]TCAAGAACAGCTGCT	2177
rs148286213	in-del	-/T	0.0023933	0.0345097	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098477	TAAAATGTAGTGTGA[-/T]ACTAGCATACTAAGA	2177
rs148300677	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10054411	CGTATATGTATATAC[A/G]TATATACATATATAC	2177
rs148404074	snp	A/T	0.17332	0.23795	intron-variant	FANCD2	GRCh38.p7	3:10055912	GAGATGGAGTCTCAC[A/T]CTGTCGCCCAGGCTT	2177
rs148444467	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096906	GGGGACCTGCCCCGA[C/T]AATCACGTAGGTTCT	2177
rs148471911	snp	C/T	3.29451e-05	0.00405851	stop-gained, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094322	GAAGCATTTCTGAAG[C/T]AATGTATGCCGCTCC	2177
rs148545267	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10063422	AGCCTGGACGACAGA[A/G]CAAGGCTCCATCTCA	2177
rs148545750	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10044975	TTATCTTTAATGACT[A/G]TATTCTGGTCTAATA	2177
rs148612270	snp	A/G	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10028774	CAATGTGTGAGGCAT[A/G]TGAGAGATATAAAGT	2177
rs148617630	snp	G/T	0.00279162	0.0372561	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086779	CACCATGCCCGGCCT[G/T]TGAACCCAGATTTTA	2177
rs148698184	snp	A/G	0.00358779	0.0422022	intron-variant	FANCD2	GRCh38.p7	3:10042113	ATATTGTCCAGGCTG[A/G]TCTTGAACTCCGGAC	2177
rs148882087	snp	A/G	0.00199481	0.0315187	intron-variant	FANCD2	GRCh38.p7	3:10059533	TTTCGGGCCAGGCAC[A/G]TAATCACCCCTGTAA	2177
rs148918400	snp	A/G	0.00755907	0.0610114	intron-variant	FANCD2	GRCh38.p7	3:10066794	CGGTGGCTCAATCTC[A/G]GCTCACTGCAACCTC	2177
rs148932502	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10056893	GGGGTCTCACTCTGT[C/T]ACACACATTGGAGTA	2177
rs149086979	snp	C/T	0.00199481	0.0315187	intron-variant	FANCD2	GRCh38.p7	3:10031939	GCAACCTCTGCCTCC[C/T]GGGTTCAAGTGATTC	2177
rs149106922	in-del	-/TC			intron-variant	FANCD2	GRCh38.p7	3:10048251	TCTGAGCTCTAAAAT[-/TC]TCTGTCTGAAATTAA	2177
rs149110498	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10080901	CACTGTTCCTACTCT[A/G]CAAAAGCCAATCTCT	2177
rs149125003	snp	G/T	0.00515222	0.0504932	missense	FANCD2	GRCh38.p7	3:10046601	GACCTGGTGATGCTT[G/T]TCATCATCTATAGCA	2177
rs149146745	snp	C/T	9.88598e-05	0.00702995	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088414	ATGAGGTCAAGTTCC[C/T]ATATGTAAGATTCCT	2177
rs149225267	snp	C/G			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027759	AAATACAAAAAATTA[C/G]CCGGGCGTGGTGGCG	2177
rs149232479	snp	A/G	0.00199481	0.0315187	intron-variant	FANCD2	GRCh38.p7	3:10044373	ATACCTTCCATCAAA[A/G]AGCCAGATGATTGGC	2177
rs149365879	in-del	-/CCC			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084852	GGAGTTTTATGATCA[-/CCC]CAGCCATAATACAAT	2177
rs149372158	snp	C/T	0.00478085	0.0486577	intron-variant, utr-variant-5-prime, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026602	TGGCTTCCTCATCTG[C/T]CCTGAGATGGGATAA	2177
rs149391800	snp	A/G	0.0154538	0.0865337	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097624	GGGTGCCCACATTTC[A/G]TATTGCTCAAACACA	2177
rs149395670	snp	A/G	0.000428611	0.0146329	synonymous-codon	FANCD2	GRCh38.p7	3:10074568	GACATCATTGTTACT[A/G]CATAATTCCCATGCT	2177
rs149408476	snp	C/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10061333	AAATTCTCCCTCTAA[C/T]CCCACCCCAACCGCC	2177
rs149427890	snp	G/T	0.00279162	0.0372561	intron-variant	FANCD2	GRCh38.p7	3:10051981	AAGACATAACTTTTG[G/T]TAGAATATTGTTTTC	2177
rs149445353	snp	A/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10068461	AAGAGCACTATAATG[A/T]GTACTATGAAACATT	2177
rs149462059	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10041717	CTATTGAAGGTAGAA[A/G]AGACTCAGCTTTCCA	2177
rs149564544	snp	A/G	4.94189e-05	0.00497062	missense	FANCD2	GRCh38.p7	3:10064730	GTTTTTCTCCGCAGT[A/G]ACTTTCCATTTCCTG	2177
rs149587682	snp	A/G	0.0611083	0.163768	intron-variant	FANCD2	GRCh38.p7	3:10054369	tatatatatatatac[A/G]tgtatatacatgtat	2177
rs149599973	snp	A/G	0.000153988	0.00877328	synonymous-codon	FANCD2	GRCh38.p7	3:10043082	GGAGAAGTTGGATCT[A/G]CAGCATTGTGTTTTG	2177
rs149618265	snp	A/C	0.00366505	0.0426508	intron-variant	FANCD2	GRCh38.p7	3:10034421	GGTTTTTAGAGAAGG[A/C]AAACTATGGTAGGAA	2177
rs149623709	snp	A/G	0.00438332	0.0466095	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093680	TGGCCTTACAAATGT[A/G]GGATCTGATATCCTG	2177
rs149642476	snp	C/T	0.00159617	0.0282053	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082644	TCTCCTGCCAGGACC[C/T]CCACTCTTCTTGATC	2177
rs149731414	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096656	TGGTCACAGGCTGCA[C/T]CCCTCATCTTAGGCA	2177
rs149885493	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10058545	TTTTAAGGATTTAAC[A/G]TCATTCTTTTGCACA	2177
rs149922376	snp	C/G	0.00318978	0.0398085	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100570	AGAGACAGGGTTTCA[C/G]CATGTTGGCCGGGCT	2177
rs150027011	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10075685	ATTAATTTTCACCTG[A/C]AATTTACACGAATGT	2177
rs150075366	snp	C/T	0.000346041	0.0131492	missense	FANCD2	GRCh38.p7	3:10028685	AGAAGACTGTCAAAA[C/T]CTGAGGATAAAGAGA	2177
rs150079582	snp	C/T	0.00478085	0.0486577	intron-variant	FANCD2	GRCh38.p7	3:10050352	GTGGCGGTCCGGGTG[C/T]GGTGGCTCATGCTTG	2177
rs150083987	snp	C/G	0.021333	0.101051	intron-variant	FANCD2	GRCh38.p7	3:10072177	AAAGAAATGATAAAT[C/G]CTTGAGGTGATGGAT	2177
rs150100340	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10044224	ATTGCCCTTCCTTCC[A/G]CTCAGCACCACTGTC	2177
rs150134181	snp	A/G	0.00636936	0.0560724	intron-variant	FANCD2	GRCh38.p7	3:10077163	ACTTGAGTCCAGGAG[A/G]TTGAGGCTGCAGTGA	2177
rs150217066	snp	A/G	0.000153988	0.00877328	missense	FANCD2	GRCh38.p7	3:10065482	AACTTGGAGGAGATT[A/G]ATGGTCTACTAGGTA	2177
rs150219250	snp	A/G/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10056457	TGTATGTAGGTTCCA[A/G/T]TTTCTCCATATCCTT	2177
rs150256384	snp	A/G	0.0314385	0.121371	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097530	ACATGGTTCTGTTCC[A/G]CCCGGCTCACCGGCG	2177
rs150308329	snp	A/G	0.00398564	0.0444627	intron-variant	FANCD2	GRCh38.p7	3:10067785	CCTGGGTGACAGAGC[A/G]AGACTCCCATCTCAA	2177
rs150415982	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10046777	AAAGCTTTACAGCTC[C/T]CATGTAAAATTTCAT	2177
rs150432259	snp	A/G	0.00597247	0.0543191	intron-variant	FANCD2	GRCh38.p7	3:10030258	CATGCCATCATGCCT[A/G]GCTAATTTTTGTATT	2177
rs150434555	snp	A/G	0.00159617	0.0282053	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088326	GTTGCCTGTTAGACC[A/G]GGAACGTCTTAGTAA	2177
rs150444770	snp	A/C/T	3.29686e-05	0.00405998	missense	FANCD2	GRCh38.p7	3:10036303	CTGCCATTATCAAAA[A/C/T]CTTATTTGAGAAGTT	2177
rs150540355	snp	C/T	0.00755907	0.0610114	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090744	ATTACAGACGTGCGC[C/T]ACTGCGCCCGGTGGT	2177
rs150595214	snp	C/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10036572	TGGTGCAGTGGCTCA[C/T]ACCTGTAATCCCAAC	2177
rs150696807	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085344	TTAGAGCTGTGATTG[A/G]ATTTGGTACTTCAGT	2177
rs150763563	in-del	-/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084464	CCAGCTGATTTTTCC[-/T]TTTTTTTTTCTTTGG	2177
rs150785408	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100211	TTTATTTACATGGTC[C/T]CCAGTTTTATTTGTA	2177
rs150838760	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10071101	CCAAATCCCCCTCTG[C/T]GAGAAACACCCAAGA	2177
rs151053030	snp	C/G	0.0379877	0.132479	intron-variant	FANCD2	GRCh38.p7	3:10045227	AGGCTGGACTGCACT[C/G]GCGTGATCTCGGCTC	2177
rs151055132	snp	A/G	0.000153988	0.00877328	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096407	TGCAGAGTCAAAGCT[A/G]TGCTCACTCTCAACA	2177
rs151067541	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10032590	GGGATTACCACATGA[G/T]CCACCTTGCCTGGCC	2177
rs151108286	snp	C/G	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10066823	TCCGCCTCCCAGGTT[C/G]AGGCAATTCTCCTTC	2177
rs151125236	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10040448	CCCTTAAGTTTCATT[A/G]ACTTGTTCTTCAGGG	2177
rs151141725	in-del	-/TA			intron-variant	FANCD2	GRCh38.p7	3:10048860	TAATTCTGTTATGAC[-/TA]TTATGGAGTGACAGT	2177
rs151224882	snp	A/C	0.00265053	0.0363076	synonymous-codon	FANCD2	GRCh38.p7	3:10063881	ATTTGCCAACCTGAT[A/C]CAACATGAAAAGCTG	2177
rs151231031	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087426	CATTTTCCCAGAACA[A/G]CCTGACTGATTTCTG	2177
rs151283886	snp	C/T	0.00755907	0.0610114	intron-variant	FANCD2	GRCh38.p7	3:10059584	AAGACAGGCGGATCA[C/T]GAGGTCAGGAGATCG	2177
rs151316403	snp	A/G	0.000153988	0.00877328	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088506	GGGATAAAGAGAAGA[A/G]CAACATCTCTAATGA	2177
rs151319288	snp	C/T	0.0577344	0.159793	downstream-variant-500B, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10102394	GTGATCTACCCGCCT[C/T]GGCCTCCCAAAGTGG	2177
rs180708527	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095433	TAGTTGCTCCTTGAG[A/T]TTGGGCAGTCCTCTA	2177
rs180713575	snp	A/G	0.00318978	0.0398085	intron-variant	FANCD2	GRCh38.p7	3:10058852	CATGTGAATTTTGGT[A/G]TGGATCTTTCTGTTT	2177
rs181014732	snp	C/T	0.00119737	0.0244387	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081654	CTGAGTCCTTTGGAG[C/T]CACTATGTTAACCCA	2177
rs181036192	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10066184	TCACTTCACATTGCC[C/T]ATGCTTTATTTTCTC	2177
rs181151949	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10035375	CACAGCCCTGTTGCT[A/G]TGATGGGTTTGGTAG	2177
rs181162686	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10053585	TTTTTTGTATTCTCA[A/G]TATTTTGTATTAATT	2177
rs181180219	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10079237	CATTAGAACAAGACT[C/G]TGTCTCAGAAATAAA	2177
rs181219364	snp	C/T	0.00031309	0.0125079	synonymous-codon	FANCD2	GRCh38.p7	3:10063797	TTTGCTCCAGGTGAC[C/T]TCCTTGTTGCAGTTG	2177
rs181226647	snp	C/T	0.00119737	0.0244387	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087807	GTGCGCACCACCGTG[C/T]CCAGCCAATTTTTGT	2177
rs181254703	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10045069	TTTTTTCTTGTTTGT[C/G]CTGCTTGCCTTTTTA	2177
rs181263646	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10040334	AGCCACCGTGCCTGG[C/T]CCCATGTACTTTCTT	2177
rs181268064	snp	G/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093756	TAGATTTGATGGGAA[G/T]TCCAGTCAGAATGTT	2177
rs181270913	snp	C/T	0.00199481	0.0315187	intron-variant	FANCD2	GRCh38.p7	3:10056947	GCAACCTCCACCTCC[C/T]AGGCTCAAGCGATCC	2177
rs181274599	snp	C/T	0.000148452	0.00861418	missense	FANCD2	GRCh38.p7	3:10074558	AGGAAGAAAAGACAT[C/T]ATTGTTACTACATAA	2177
rs181279000	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101352	CTGTTTGCCTTTCTT[A/G]CTGGTAGGATCCTTT	2177
rs181285888	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10047858	GATAAGCAACTCTTA[A/G]GTTGTGTACTAACTG	2177
rs181290969	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10029510	GACCATGTCTCAAAA[A/G]GGGAGTGGGGGGCGG	2177
rs181473323	snp	C/T	0.02016	0.0983543	intron-variant	FANCD2	GRCh38.p7	3:10067766	TTGTGCCACTGCACT[C/T]CAGCCTGGGTGACAG	2177
rs181646854	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10035713	TTTTTCCTCTTCTCC[C/T]CTACTGTTAATCTTT	2177
rs181661934	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10071836	ACAGTCTCGGCTTAC[G/T]GCGACCTCTGCCTCC	2177
rs181800267	snp	C/G/T	0.0023933	0.0345097	intron-variant	FANCD2	GRCh38.p7	3:10031241	AGGCACGGTGGCTCA[C/G/T]GCCTGTAATCCCAGC	2177
rs181806441	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10046816	AGTCCATTGTTCAAA[C/T]CCATTGAGATTTTTG	2177
rs181838959	snp	A/G	1.64898e-05	0.00287135	utr-variant-5-prime	FANCD2	GRCh38.p7	3:10028655	CACAAGACATTGGTC[A/G]AAATGGTTTCCAAAA	2177
rs181851717	snp	A/G/T	0.0021266	0.0325397	intron-variant	FANCD2	GRCh38.p7	3:10062128	GTATAATAATAATTT[A/G/T]AAAAAAAATTCTTTG	2177
rs181877289	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FANCD2, FANCD2OS	GRCh38.p7	3:10100057	GCCAGGCATGGTGAC[A/G]CATGCCTGTGGTCCC	2177
rs181978096	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100741	CCTATGTCATATACA[C/T]GCAGTAGAGCTGGAG	2177
rs181985499	snp	G/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10029270	TTTGAGGGGCTAAGG[G/T]GAGAGGGTCACCTAA	2177
rs181987077	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10078322	TAGCATGGGTGCAGC[C/T]GTATTGCCAGACAAT	2177
rs181993814	snp	C/T	0.00279162	0.0372561	intron-variant	FANCD2	GRCh38.p7	3:10062765	GCCAAGGCTGGAGTG[C/T]GGTGGTGCTTCCCGG	2177
rs182016312	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10074959	ACCTAGATTATTTTT[A/G]TAGAGGAGCACTCTT	2177
rs182067891	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10040865	GCCTGATGCCAGCTC[A/G]TCTCCTTTTGTATAG	2177
rs182095969	snp	A/G	0.00438332	0.0466095	intron-variant	FANCD2	GRCh38.p7	3:10044354	GTCTCTATTAATTCT[A/G]GAAATACCTTCCATC	2177
rs182181301	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10089438	TTCAAGGGCTCTCAG[C/G]TAATATATTTGAGAG	2177
rs182295557	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094720	TTAAAAAAAAAAAAG[C/G]TCATTTGTGTCATAA	2177
rs182347259	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025122	CTGCACCTGGCTAAT[A/G]TTTAAATTTTTTTGT	2177
rs182423609	snp	G/T	0.0562307	0.157967	intron-variant	FANCD2	GRCh38.p7	3:10032493	AGGGGGGGAGATGGG[G/T]GGGTGGTCTCACTTT	2177
rs182617509	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085613	GCCAAGATGGTCTCC[A/G]TGTGTTGACCTCGTT	2177
rs182673439	snp	C/T	3.30011e-05	0.00406195	intron-variant	FANCD2	GRCh38.p7	3:10073383	GGAATGATGGGTATC[C/T]GTGAAGGTTTGTGAC	2177
rs182673490	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10037384	GTGAATAGGCATGCT[C/T]GTACGTTGCTAGTGA	2177
rs182677780	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10054775	GGCCTGAGCCACCGC[A/G]CCCGGCCACAACCAT	2177
rs182706327	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10059422	TATAGAAATAATAAC[A/C]ATAAAAGATATTATT	2177
rs182712901	snp	A/T	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10033533	GTTTTCTTATGAAAA[A/T]ATAAATATCCAGAAA	2177
rs182719538	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10050395	TTTGGGAGGCCAAGG[C/T]GGGCAAATCACGAGG	2177
rs182722558	snp	C/G	0.00119737	0.0244387	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095841	TCTGTTACTTACTTC[C/G]TCCTCTGGTTCTAAA	2177
rs182726983	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10076104	ATAAATGTGTATTGA[A/G]TGAGCAGTTTGCAGT	2177
rs182852266	snp	C/G	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091162	CTTGGCTCACTGCAG[C/G]CTTTGCCTTCTGGGC	2177
rs182864098	snp	C/T	0.00597247	0.0543191	intron-variant	FANCD2	GRCh38.p7	3:10074006	GCTGGAGTGCAGTGG[C/T]ACGATCTTGGCTCAC	2177
rs182929401	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10055119	GCTTCAAATCAGCAA[C/T]ATAAAACTACTTCAC	2177
rs183013082	snp	A/G	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10029960	GGCTGATTTTTTTGT[A/G]TCTTTAGTAGAGACG	2177
rs183015594	snp	G/T	0.00716266	0.059414	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026803	ACGTGCTGACAAGAC[G/T]TAGTTTTTCCATCTG	2177
rs183138323	snp	G/T	0.00279162	0.0372561	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086005	CTTTAAAATAACCTG[G/T]GTGTCTTTCAGTAGT	2177
rs183157403	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10068651	AAAAAAAAAGCCTAA[A/C]ATTTATATAGAACCA	2177
rs183218655	snp	A/G	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10032141	TGAGCCACTGTGCTG[A/G]GTCGGAAATATGCAT	2177
rs183226884	snp	A/C	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10048458	ACAGGCACACACCAC[A/C]ACGCCCGGTTAATTT	2177
rs183233410	snp	A/G	0.00318978	0.0398085	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084456	CACCATGCCCAGCTG[A/G]TTTTTCCTTTTTTTT	2177
rs183256846	snp	A/G	1.64781e-05	0.00287033	synonymous-codon	FANCD2	GRCh38.p7	3:10064367	GAAGGAATGGGTTGG[A/G]CATACCATCTGTAAT	2177
rs183259704	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090065	TTCATTGCTTTTTCC[A/G]TACTACCATAACACC	2177
rs183267315	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10030272	TGGCTAATTTTTGTA[A/T]TTTTAGTAGAGAAGG	2177
rs183274184	snp	C/T	0.0016444	0.0286268	intron-variant	FANCD2	GRCh38.p7	3:10045542	TTTATTGAACCTTTC[C/T]TGTATTGATGTATTG	2177
rs183296350	snp	G/T	0.00199481	0.0315187	intron-variant	FANCD2	GRCh38.p7	3:10042186	CAGGCTTGAGCCACC[G/T]TGCCTGGCCCACAGG	2177
rs183305533	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10037967	TTTAATTTTTTCAGA[A/G]TCCTGATACAGTAAT	2177
rs183326211	snp	A/G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10064992	AGACAAATGGTATTT[A/G/T]GAGAGGTTAGGGAGA	2177
rs183413361	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10069201	GCATAGCAAAGGAAA[C/T]ACCAAAGTGAAGAGA	2177
rs183414970	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10079455	GGACTACAGGCGCGC[A/G]CCACCACACCCAGCT	2177
rs183489030	snp	C/T	0.00438332	0.0466095	intron-variant	FANCD2	GRCh38.p7	3:10079381	GCAATCTCGGCTCAC[C/T]GCAGCCTCTGCCTCC	2177
rs183511434	snp	C/T	0.00636936	0.0560724	intron-variant	FANCD2	GRCh38.p7	3:10045396	GATGGTCTCAATCTC[C/T]TGACCTCATGATCTG	2177
rs183514621	snp	C/T	0.0111196	0.0737302	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027978	AGCACTTTGGGAGGC[C/T]GAGGTGGGTGGATCA	2177
rs183523591	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10043403	TGTCATTTGCTCCAG[G/T]GTACATGGCAGGAAC	2177
rs183528545	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10061097	CAACTTAATCACCAG[A/T]CACCTGCAAGTTAGC	2177
rs183529940	snp	G/T	0.0023933	0.0345097	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098352	TGTCCTTTAGCCTCC[G/T]CATGGCCATTCGTGC	2177
rs183533956	snp	C/G	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10076966	ACATTGGCCAGGCTG[C/G]TCTCAGACTCCTGAC	2177
rs183652685	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093508	TTGGAGAAGCCAGTT[G/T]TCCTATGAATTTGAA	2177
rs183778817	snp	A/G	0.000132387	0.00813485	missense	FANCD2	GRCh38.p7	3:10043137	GTAAAGTTGAAAAGT[A/G]AAGGACGAGCAAGGT	2177
rs183844109	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10076497	TTATTATATGACAGA[A/G]CATAATAGCTATCCT	2177
rs183906839	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10054456	ATATACATATATATA[C/T]ATATATATATATATA	2177
rs183923226	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10056418	TTCCATAGCAGCTGC[A/G]TAATTTTACATTCCC	2177
rs183943710	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10074475	AAGTTTTTATTAAAA[A/T]TCGATTAATATAGAA	2177
rs183971233	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10059978	GAGTTCACCAGCCTA[A/G]CCAACATGGTGAAAC	2177
rs184022219	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096272	GTTTCTATAAGAAAT[A/G]TGAAGGCATGATGAT	2177
rs184048182	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027046	CTCAAAAAGTTTTGT[A/G]GGAAATAAATGAATT	2177
rs184060118	snp	A/C	6.59783e-05	0.00574324	intron-variant	FANCD2	GRCh38.p7	3:10036269	TCATCTCCTAACTCC[A/C]TATGTCTTCTTTTTT	2177
rs184093842	snp	A/G	0.00279162	0.0372561	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10099281	AATAGAAGTTCTTAC[A/G]CTTTTTTGTGGTACA	2177
rs184100946	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10077536	CTCCAGCCTGGGTGA[C/T]GGAACAAGACTCTGT	2177
rs184116581	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10072548	CCTCCCAAAGTGCTT[A/G]GGGTTACAGGCGCGA	2177
rs184194287	snp	G/T	0.00478085	0.0486577	intron-variant	FANCD2	GRCh38.p7	3:10070156	CTGCCCGGCTGCCCC[G/T]TATGAGAAGTGAGGA	2177
rs184209377	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10035002	GCTGACAGAATTTCA[A/T]ATCTCTACCTCTCCC	2177
rs184221908	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094003	TTATCCTCAGATAGA[A/G]CTCCCCTCTACTCTA	2177
rs184227835	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10074934	CTACTACTACTACTA[A/C]TAATAAGCTACCTAG	2177
rs184254596	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10053498	TAACCTGCACATTGT[A/G]CACATGTACCCTAAA	2177
rs184328551	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087752	CTCCCAGGTTCAAAC[A/G]ATTCTCCTGCCTCAG	2177
rs184424788	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10031142	GAAACTTTCATTCTG[A/G]TTGTGTTTTACATTT	2177
rs184433000	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10046335	TGGGATTACAGATGT[A/G]AGCCACTGTGCCTGG	2177
rs184661203	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10046135	CTCGGCTCACTGTAA[C/G]CTCTGCCTCCCGGGT	2177
rs184800216	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10068599	ATTCAAGGCAATCCC[C/T]ATTAAAATACCAATG	2177
rs184802482	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10030785	CGTGTCTGTAATCTC[A/G]GCTACTCGGGAGGCT	2177
rs184831005	snp	A/G	0.00318978	0.0398085	intron-variant	FANCD2	GRCh38.p7	3:10034082	GTAATCCCAGCACTT[A/G]GGAGGCTGAGGAGGG	2177
rs184861001	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10065291	AAGACTCTGTCTCAA[A/G]AAAAGAAGTTGTGTT	2177
rs184879342	snp	A/C/G			intron-variant	FANCD2	GRCh38.p7	3:10069707	AACCGCGAGTGATCC[A/C/G]CTAGCCTCAGCCTCC	2177
rs184930781	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10028504	CCTAGGTTTAGGTAG[C/T]ATTAATATGGAGATG	2177
rs184945990	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10061450	GTCAGTGAAGCCATA[C/G]TGGTTGCCCAGGGTC	2177
rs185020025	snp	C/T	4.97038e-05	0.00498492	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081055	CCTTAGTTTCTGAGA[C/T]GCTATCCAGCAGTTT	2177
rs185020978	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10072479	AGATAGGGTTTCACC[A/G]TGTTGGCCAGGCTGG	2177
rs185027909	snp	G/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10066140	GTTATATGAACCTCC[G/T]TAGGTAGCCAAATGA	2177
rs185047839	snp	A/G	0.000399281	0.0141238	missense	FANCD2	GRCh38.p7	3:10043519	GCAGCGGTCAGAGCT[A/G]TATTATTCTCCTCTT	2177
rs185068322	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10065690	AATTGTTGCAAAAAC[C/T]TTCTAGTTATATTTG	2177
rs185085575	snp	C/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10047014	CACTCTTTAGCCATT[C/G]AAAACTGTGGACTTT	2177
rs185101322	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10057392	TTTTTTTGAGATGGA[A/G]TCTCACTCTGTCACT	2177
rs185129151	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10029342	CCATCTCTACAAAAA[A/T]TTTTTTTAATTAGCT	2177
rs185137247	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10044889	TATAAATATAATTTG[C/T]ATTCTTACTTTTTTT	2177
rs185167872	snp	C/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10080801	AGAAGGAGTCTATTG[C/T]CCTACATTTGTCAAC	2177
rs185174772	snp	A/G	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10078576	AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTTGT	2177
rs185182530	snp	C/T	0.00279162	0.0372561	intron-variant	FANCD2	GRCh38.p7	3:10063418	CTCCAGCCTGGACGA[C/T]AGAGCAAGGCTCCAT	2177
rs185210508	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10077963	AACTTGGGCCCAGGA[A/G]TTCAAGGCTGGAATA	2177
rs185312880	snp	C/T	0.00119737	0.0244387	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100396	CTTCTTTTTTTGAGA[C/T]GGAGTCTCCCTCTGT	2177
rs185319192	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095514	CCTCTAGAAACTTCT[G/T]GGGTGACAGAAATAG	2177
rs185323571	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10075631	TGGGATTTCATCAGA[G/T]AGTAGAATTTCTCTA	2177
rs185334873	snp	G/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10062457	ATGTTGGCCCCGCTG[G/T]TCCTGAACTCCTGAA	2177
rs185373575	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	FANCD2, CIDECP	GRCh38.p7	3:10026090	CGCTCTCCAGCAGGA[G/T]GGACACGTAGTGGCG	2177
rs185383953	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10042148	TTTTCCACCCCCCTC[A/G]GCCTCCCAAAGTGCT	2177
rs185391313	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10059038	TTTTATTTTGAGACA[A/G]TGTCTGGCTCTGTCA	2177
rs185575926	snp	A/C	0.0741063	0.177655	intron-variant	FANCD2	GRCh38.p7	3:10070369	GCCGCCCCGTCCGGG[A/C]GGGAGGTCAGGGGGT	2177
rs185649879	snp	A/G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10035599	CTTTTCCTCCTCCTC[A/G/T]TCTCTTTTATTAAGT	2177
rs185656736	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10053587	TTTTGTATTCTCAGT[A/G]TTTTGTATTAATTTT	2177
rs185705102	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10048172	CCTGGGTCTCAAGAA[A/G]GCTCAATTCTAGTCC	2177
rs185714261	snp	G/T	0.0023933	0.0345097	intron-variant	FANCD2	GRCh38.p7	3:10056003	CTTGCCTCAGCCTCC[G/T]GAGTAGCTGGGATTA	2177
rs185724291	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10068261	AAAGACTCCACCAAA[A/G]AACTATTAGATAAAT	2177
rs185793030	snp	A/G	0.000399281	0.0141238	missense	FANCD2	GRCh38.p7	3:10036293	CTTTTTTAGCCTGCC[A/G]TTATCAAAACCTTAT	2177
rs185819457	snp	C/T	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10074033	TCACTGCAACCTCCA[C/T]CTCCCGGGTTCAAGC	2177
rs185838244	snp	A/G	0.00318978	0.0398085	intron-variant	FANCD2	GRCh38.p7	3:10038909	TTAAGCACTTACTGC[A/G]TTGATGTTATTAGTG	2177
rs185866952	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101452	GTGCAGTGCTGCAAT[A/C]TTGGCTCACTGCAAC	2177
rs185884924	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10089279	AGCAAGAGCGAAACT[C/G]CATCTCAAAAAAAAA	2177
rs185891324	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10072133	ATTTAAAAATAACTA[A/C]AATAGTATAATTGGA	2177
rs185898677	snp	A/G	0.00787448	0.0622514	intron-variant	FANCD2	GRCh38.p7	3:10072847	ATTGGTACACATTGA[A/G]CTTCAGCCTGCTGTT	2177
rs185930260	snp	C/T	0.0283406	0.115616	intron-variant	FANCD2	GRCh38.p7	3:10054514	TTTGAGATGGAGTCT[C/T]GCACTGTCACCCAGG	2177
rs185931639	snp	A/G	0.00636936	0.0560724	intron-variant	FANCD2	GRCh38.p7	3:10054133	GGGAGGATCCATTGA[A/G]CCCAGGAAGTTGAGG	2177
rs185981261	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081787	ATGAGCTGAACACTG[C/T]GAGCTGGGCTATTCC	2177
rs186011151	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10047252	ATTATTTTATCTTGC[A/C]GTTCTTTCTGTGTTT	2177
rs186020617	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10089630	ACCCACCACCACACC[C/T]GGCTAATTTTTGTAT	2177
rs186385181	snp	C/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10048559	AACCGCCTGCCTCAG[C/G]CTCTCAAAGTGCTGG	2177
rs186428466	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084983	CATGTATTGATAGGG[A/G]CCTGGCCAAAATGAT	2177
rs186436668	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10068710	CTGAGTAAAATGAAT[C/G]AAACTGGAGGAATCG	2177
rs186457997	snp	C/G/T	0.0154717	0.0867355	intron-variant	FANCD2	GRCh38.p7	3:10031299	ACGAGGTCAGGAGAT[C/G/T]GAGACCATCTTGGCT	2177
rs186528371	snp	A/G	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10064146	ATGATGATGGCTATT[A/G]TCTGTCTGAGAGCCC	2177
rs186529436	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10029608	ATTTTACTAGGTTTT[C/T]TGGGAACAGGTGGTG	2177
rs186545410	snp	G/T	0.00199481	0.0315187	intron-variant	FANCD2	GRCh38.p7	3:10040344	CCTGGCCCCATGTAC[G/T]TTCTTTTAAATGGTA	2177
rs186585888	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025707	ACGAAAGGGTGGGAT[A/G]GGATAGTTCATAGGT	2177
rs186586094	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10079680	CTGTTCTTTACTTGA[A/G]TTTTGGTTTCAACAG	2177
rs186601429	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10065145	AATACAAAAATTAGC[C/T]GGGCAGTGTGGCATG	2177
rs186618182	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10030319	TCAGGCTGGTCTCAA[A/G]CTCCTGACCTCCGGT	2177
rs186621666	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10045913	CCTAGTAATTTTCCT[A/G]GTAATACTGAAAATA	2177
rs186657770	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10028166	CCCTCATAGAACCTG[C/T]ACTTTTATAGCACTT	2177
rs186663304	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10045312	TAGCTGGGACTACAG[A/G]CACCTGCCACCACGC	2177
rs186663908	snp	A/G	0.000205648	0.0101381	intron-variant	FANCD2	GRCh38.p7	3:10043447	GTTCTTTTCTGGTAC[A/G]TAGAAGAGTAATTTT	2177
rs186669893	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10061157	CACAAAGCCCTCTTC[G/T]GCATACAGCATACAT	2177
rs186711125	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098379	GTGCTTGGTGTGATA[A/G]TGCTTAGATACCTTA	2177
rs186715825	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10077429	GCATGGTGGTGGGCA[C/T]CTGTAATGCCAGCTA	2177
rs186744042	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10079284	GTCTGAAACAGAAAA[C/T]AGAAAGGCACTTGGA	2177
rs186750908	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10059521	CAACCTTCTCCATTT[C/T]GGGCCAGGCACGTAA	2177
rs186757611	snp	C/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10079452	TGGGGACTACAGGCG[C/T]GCGCCACCACACCCA	2177
rs186773024	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10024619	TCAGTTACAAATTAC[A/T]AAGCTTTATCTTTAT	2177
rs186914908	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082882	ACTTAAAAGCAGTGC[C/G]TGACAAAAACTTTGA	2177
rs187024247	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10035818	TGTTCCTCCTGAGAG[C/T]TCCCCTTGCAAGTTA	2177
rs187283008	snp	A/G	0.00318978	0.0398085	intron-variant	FANCD2	GRCh38.p7	3:10037423	ATTAGTTCAGGCATC[A/G]ATTCGGAAGAGCAAT	2177
rs187290625	snp	A/T	0.00279162	0.0372561	intron-variant	FANCD2	GRCh38.p7	3:10054856	ATTTTTTTTAATTAA[A/T]AAAAAAACTTTTGGA	2177
rs187313930	snp	C/T	0.00438332	0.0466095	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090619	ATGCGCCACCACACC[C/T]GGCTAATTTTTATAT	2177
rs187315905	snp	A/C	0.00398564	0.0444627	intron-variant	FANCD2	GRCh38.p7	3:10032202	GTGGTTTGCAGGCAA[A/C]AGCTTGAGAGACACT	2177
rs187322860	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10073455	TTTTACAAAGAAAAA[A/G]AAATTAGGAAACAGC	2177
rs187406076	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094850	ACATATTTAGCAAGT[A/T]GAACAAAATACTCAC	2177
rs187422340	snp	C/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10057842	CTTAGTTTTAAATGA[C/G]GACCACCCAACAAGA	2177
rs187439967	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10030078	AGGCTTGAGCCACCA[C/T]GCCTGGCCCATTATA	2177
rs187442408	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086347	GGACAAGGGAGGTGA[C/T]ATGATCTCAGGGGCA	2177
rs187446230	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10045448	GCTGGGATTATAGGC[A/G]TGAGCCACCATGCCT	2177
rs187448960	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10069319	TATTCGGATTGAAAA[A/G]TGGGTAAAAGGTCTG	2177
rs187453586	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095990	GGCTGGACAGTGAAT[A/G]TTTAAGGAATTCTCT	2177
rs187491254	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10033847	GGACTACAGGCGCCC[A/G]CCACCATGCCTGACT	2177
rs187498667	snp	A/G	0.0119091	0.0762411	intron-variant	FANCD2	GRCh38.p7	3:10050487	AATTAGCCGGGCATC[A/G]TGGCGGTCGCCTGTA	2177
rs187524733	snp	G/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10074124	CTAATTTTTGTATTT[G/T]TAGTAGAGACGGGGT	2177
rs187584264	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091327	CTCAAGCAATCCTCC[C/T]GCCTCAGCCTCCCAA	2177
rs187590767	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10074008	TGGAGTGCAGTGGCA[C/T]GATCTTGGCTCACTG	2177
rs187667215	snp	A/G	0.0023933	0.0345097	intron-variant	FANCD2	GRCh38.p7	3:10041110	GAGATGGGAGGATCA[A/G]TTGAGCGTGGAAGGT	2177
rs187668789	snp	C/G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10074978	AGGAGCACTCTTCTG[C/G/T]TTCTTAGAAGTCAAT	2177
rs187670254	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085633	TTGACCTCGTTATTC[G/T]CCCGCCTCAGCCTCC	2177
rs187675742	snp	A/G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10050353	TGGCGGTCCGGGTGC[A/G/T]GTGGCTCATGCTTGT	2177
rs187832940	snp	A/G/T	6.59189e-05	0.00574071	intron-variant	FANCD2	GRCh38.p7	3:10065362	TAATACACCTATGAA[A/G/T]TGTGGTCTAGAAATT	2177
rs187860884	snp	C/G	0.00119737	0.0244387	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092999	GCCCAGCCTCATCCA[C/G]TCTTTCTTAAGTCTT	2177
rs187873909	snp	C/T	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027412	AAGAACACCTTTGTG[C/T]AAAGGCACTGAGACC	2177
rs187963558	snp	A/C	0.02016	0.0983543	intron-variant	FANCD2	GRCh38.p7	3:10069048	TACTAACAACAACAA[A/C]AAAAAACATTCAGAA	2177
rs188102231	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10080509	GGCACAGTGGCTCAC[A/G]CCTTTAACCCCAACA	2177
rs188110634	snp	C/T	0.00398564	0.0444627	intron-variant	FANCD2	GRCh38.p7	3:10030825	GAATTGCTTGAACCC[C/T]GGAGGTGGAGGTTGC	2177
rs188191066	snp	G/T	0.0379877	0.132479	intron-variant	FANCD2	GRCh38.p7	3:10047168	GTGGTTTGGGGTTTG[G/T]GTTAGGAGCTAATGA	2177
rs188329749	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10042215	GGTCTGTTTTTAAGC[A/G]GTAAGTTTTGAGTGG	2177
rs188367142	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093732	TGTGGGAATAGCCTG[C/T]ATTAGCCCTAGATTT	2177
rs188375397	snp	C/T	0.00160435	0.0282772	missense	FANCD2	GRCh38.p7	3:10074537	CCCCATAGGAGTTCA[C/T]AGGGAAGGAAGAAAA	2177
rs188383800	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10055414	TAAATGGAATCATAC[A/G]ATATGTATCCTTTTG	2177
rs188403544	snp	A/C/G	3.33941e-05	0.00408609	utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101306	TGTCTCTGCCAGCCT[A/C/G]TGATCATTTTGTGTT	2177
rs188413690	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10056422	ATAGCAGCTGCATAA[C/T]TTTACATTCCCACCA	2177
rs188505561	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026919	TAACCATTATTAGAA[G/T]TCATTATAATCATCA	2177
rs188618961	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10059630	ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA	2177
rs188624305	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096715	AAACAATGCCTCAGA[C/T]ATAAAGGAGTCAGAC	2177
rs188668658	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10064651	ATGTTGTGTTTGAAA[G/T]TGGTTTGCTCTAGTG	2177
rs188694768	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10038666	ACTCACTGCAACCTC[C/T]GCCTTCTGGGTTCAA	2177
rs188758267	snp	A/G	0.00398564	0.0444627	intron-variant	FANCD2	GRCh38.p7	3:10038014	TACTTATTTTGAGAC[A/G]GAATCTCACTCTGTT	2177
rs188845308	snp	A/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10035626	AAGTAGACAATACAT[A/T]GATATGATTTAAATA	2177
rs188854474	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10053624	CTTGAAATTTGCTAG[A/G]AAAAAAAAAACAAGC	2177
rs188909356	snp	A/C	0.00159617	0.0282053	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088120	CTGCTATTGGCCAGC[A/C]CAGGAGGAACAAGAT	2177
rs188916674	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10071095	ACCCTGCCAAATCCC[C/T]CTCTGCGAGAAACAC	2177
rs188962228	snp	A/C			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085572	AATTTTTGTATTTTT[A/C]GTAGAGACGGGATTT	2177
rs189086962	snp	C/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10031231	AAAGGAGGCCAGGCA[C/T]GGTGGCTCACGCCTG	2177
rs189134008	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10080956	TTTTTATCCCTCTGT[C/G]AGAATACAGTCTTAG	2177
rs189140238	snp	A/C	0.00199481	0.0315187	intron-variant	FANCD2	GRCh38.p7	3:10066055	TTAGTTCCCACAAGA[A/C]TCCCTAGAAGTCTTC	2177
rs189147450	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10038967	TTCAGTTTTTAAGAT[G/T]TATTAACATTGTCTT	2177
rs189205221	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10053521	ACCCTAAAACTTACA[A/G]TATAATAATAATAAA	2177
rs189210051	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10076643	GAACTCCTGGGTTCA[A/T]GGATCAAGTGATCCT	2177
rs189299621	snp	A/T	1.64743e-05	0.00287	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087116	TTGCATTTGTTTGTT[A/T]TTCTTGTCTCCTTAC	2177
rs189306515	snp	C/T	0.342358	0.232314	intron-variant	FANCD2	GRCh38.p7	3:10069709	CCGCGAGTGATCCGC[C/T]AGCCTCAGCCTCCCG	2177
rs189320600	snp	C/T	0.00119737	0.0244387	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087795	CTGGGATTACAGGTG[C/T]GCACCACCGTGCCCA	2177
rs189329374	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10028982	CTTTTTCTGCTATAC[A/G]TCATTTAGGTGTTGA	2177
rs189336608	snp	A/C	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10044619	ATGATTGAGTTCCTT[A/C]GGTGCTGATTGGTTG	2177
rs189346903	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10062755	CAACTCTGTCGCCAA[A/G]GCTGGAGTGCGGTGG	2177
rs189443562	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10056010	CAGCCTCCTGAGTAG[C/T]TGGGATTATAGGCAC	2177
rs189446835	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10070315	GCCCGGCAGCCACCC[C/T]GTCCGGGAGGGAGGT	2177
rs189447494	snp	A/G	0.00318978	0.0398085	intron-variant	FANCD2	GRCh38.p7	3:10031279	GTGGCCAAGGCGGGC[A/G]GATCACGAGGTCAGG	2177
rs189483244	snp	G/T	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10035088	TTTAAATATTATGTA[G/T]TTAACCAATTTTATT	2177
rs189513602	snp	A/G	0.0154538	0.0865337	intron-variant	FANCD2	GRCh38.p7	3:10070196	CCCGGCAACCGCCCC[A/G]TCTGAGAAGTGAGGA	2177
rs189658301	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081813	ATTCCATGATACCTT[A/C]ATGGAAACAGTGGGA	2177
rs189730158	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10047269	TTCTTTCTGTGTTTA[C/T]TTCTGCCAATTATAC	2177
rs189758149	snp	A/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025975	AGGCAAACTGACACA[A/T]CGCCTGCACTTTCTT	2177
rs189766023	snp	C/T	0.000215341	0.0103742	intron-variant	FANCD2	GRCh38.p7	3:10041758	CAGCTTTCCAACCTC[C/T]CAGAACAAGTGTCAG	2177
rs189895537	snp	C/G	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10044973	TGTTATCTTTAATGA[C/G]TGTATTCTGGTCTAA	2177
rs189978498	snp	A/C/G	0.00020072	0.0100162	intron-variant	FANCD2	GRCh38.p7	3:10043619	GGAACTTTGATTATC[A/C/G]AGGAGGAAATGAGTG	2177
rs189980369	snp	A/C	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10079087	CTCTACTAAAAATAC[A/C]AAAAAAATTAGCCAG	2177
rs189988503	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10063690	AGACATAGAGCTTTG[A/C]CAGTAAAATCAGAAA	2177
rs190008893	snp	C/T	0.00318978	0.0398085	intron-variant	FANCD2	GRCh38.p7	3:10036834	CTTTTCTTTACCTTT[C/T]AAATTTTGTAGTGTA	2177
rs190011650	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10024969	GTCACCCAGGCTGGA[A/C]CAAAAAGGTCGAGGC	2177
rs190034221	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10057460	ACCTCCGCCTCCCAG[G/T]TTCAAGTGATTCTCC	2177
rs190052766	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10059060	GCTCTGTCACCCAGG[C/G]TAGAGTACAGTGATG	2177
rs190130571	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10075997	TGGCCTCCCAAAGTG[C/T]TGGGATTACAGGTGT	2177
rs190136953	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026216	AGCTGGCTCCCAGCC[A/G]GTGATGGGCGAGCTT	2177
rs190141278	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10042178	TGGGATTACAGGCTT[C/G]AGCCACCGTGCCTGG	2177
rs190191504	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100423	CTGTCGCCCAGGCTA[C/G]CATGCAGTGGTGCAG	2177
rs190220233	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10028540	CCCTCTGATTTTGGA[C/T]AGAGCAGTTTTCTTT	2177
rs190222433	snp	A/T	0.00636936	0.0560724	intron-variant, downstream-variant-500B	FANCD2, FANCD2OS	GRCh38.p7	3:10100029	TCTCTACAGAAAAAA[A/T]TTTTTTGAGCTAGCC	2177
rs190275884	snp	C/T	0.00119737	0.0244387	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090673	CCATGTTGGCCAGGC[C/T]AGTCTCGAACTCCTG	2177
rs190383140	snp	A/C	0.0256215	0.110247	intron-variant	FANCD2	GRCh38.p7	3:10074937	CTACTACTACTACTA[A/C]TAAGCTACCTAGATT	2177
rs190531212	snp	C/G/T	0.000104763	0.00723688	intron-variant	FANCD2	GRCh38.p7	3:10034664	TTAAACTAAAAATTT[C/G/T]ATTCTTTTTTATTTT	2177
rs190616016	snp	A/G	0.00358779	0.0422022	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083615	GTCCACCGACCAGGC[A/G]CAGTGGCTCACGCCT	2177
rs190626337	snp	A/C	0.00279162	0.0372561	intron-variant	FANCD2	GRCh38.p7	3:10068543	tggatcggaagaatt[A/C]atattgttaaaattt	2177
rs190659197	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10048357	TGCCCAGGCTGGAGT[A/G]CAGTGGTGCTATCTC	2177
rs190699380	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10030207	GTTCAAGCGATTCTC[A/C]TGGCTCAGCCGCCCA	2177
rs190705444	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10045461	GCGTGAGCCACCATG[A/C]CTAGCATGGCTTATT	2177
rs190725100	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10049782	ATTCTCTGGTAAAGT[A/G]CTATAGATATAACAG	2177
rs190769351	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10079454	GGGACTACAGGCGCG[C/T]GCCACCACACCCAGC	2177
rs190777319	snp	A/G	9.88386e-05	0.00702919	missense	FANCD2	GRCh38.p7	3:10064760	GTGAAAGCACTGTAC[A/G]GACTGGAAGAATACG	2177
rs190785362	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10089383	TACAGACAGTAGATA[C/T]AATCATTCATTCAAT	2177
rs190818204	snp	A/G	0.00279162	0.0372561	intron-variant	FANCD2	GRCh38.p7	3:10029362	TTTAATTAGCTGGGC[A/G]TGGTGGTTTGTGCCT	2177
rs190885387	snp	A/G	0.00159617	0.0282053	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10089733	TCGGCCTCTCAAAGT[A/G]CTGGGATTACAGGCA	2177
rs190959915	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10058228	GTCTCCCTTTTCCAC[C/T]GTGTGGCACTGGGCA	2177
rs190982919	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10068956	TGCAGAAGAATGAAA[C/G]TAGACCCCTATCTCT	2177
rs190990145	snp	A/G	0.00157435	0.0280125	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095282	ATTCCAAGGTAAGAA[A/G]GGGAGCAGGTTCTAT	2177
rs191055739	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10031316	AGACCATCTTGGCTA[A/G]CATGGTGAAACCCCG	2177
rs191231166	snp	C/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027803	CCAGCTACTTGGGAA[C/G]CTGAGGCAGGAGAAT	2177
rs191386799	snp	C/T	0.00011533	0.00759287	intron-variant	FANCD2	GRCh38.p7	3:10039718	TAGTGTCTTCTACTG[C/T]AGGACCTCACCACCA	2177
rs191393228	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10056188	CCGGCCCCCATTCTT[G/T]GTTTATACCACATTT	2177
rs191465938	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101902	CTTAGGCTTGTACCA[A/G]TTTTACAAATAAATT	2177
rs191474336	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10080001	CTCACTGCAACTTCC[A/G]CCTCCTGGGTTCAAG	2177
rs191508170	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10045334	CCACCACGCCCGGCT[A/G]ATTTTTTGTATTTTT	2177
rs191522333	snp	C/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10061205	AAATCCCCAGCAAGC[C/T]GTTGTTTCCTTGCAG	2177
rs191533278	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10079351	GCTGTGTCTCCCAGG[C/G]TGGAGTGCAGTGGTG	2177
rs191614064	snp	A/G	6.58957e-05	0.00573964	intron-variant, synonymous-codon	FANCD2, FANCD2OS	GRCh38.p7	3:10098926	TTGTCAAATGCTTCT[A/G]TGCCCATTTCCATTC	2177
rs191625465	snp	A/G	0.00318978	0.0398085	intron-variant	FANCD2	GRCh38.p7	3:10077437	GTGGGCACCTGTAAT[A/G]CCAGCTACTTGGGAG	2177
rs191753401	snp	C/T			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027003	GAATCCCAGTTCTGC[C/T]CGTGATGATGAGAAT	2177
rs191758039	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10029929	GCTGGGATTACAGGC[A/G]CCAGCCACCATGCCC	2177
rs191772286	snp	A/G	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10059675	GGCGTGGTTGGTGGC[A/G]GGCACCTGTAGTCCC	2177
rs191786004	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096225	CGTTGGCCCATACTG[G/T]CAGGGCTTGTGTTCT	2177
rs191800021	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10064233	CACAATAGTGAGATA[C/T]TTATTATTACTTTCT	2177
rs191828910	snp	C/T	0.00279162	0.0372561	intron-variant	FANCD2	GRCh38.p7	3:10054923	ATATAGAAGAGTATT[C/T]AGTGAAAAATAACTC	2177
rs191868905	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10035984	TCCAATAGCATATTC[C/T]AAAAATGAAGACATA	2177
rs191878955	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10072139	AAATAACTAAAATAG[A/T]ATAATTGGATTGTTT	2177
rs191984293	snp	A/T	0.00517822	0.0506191	intron-variant	FANCD2	GRCh38.p7	3:10076492	TGACTTTATTATATG[A/T]CAGAGCATAATAGCT	2177
rs192062008	snp	A/C	8.41078e-05	0.00648435	intron-variant	FANCD2	GRCh38.p7	3:10043022	TATGAATGAGCAGAA[A/C]ACCATAGCTAATATT	2177
rs192103276	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10037498	CCTAATGTCATGTCT[C/T]CTCATTTATCCTAAG	2177
rs192178625	snp	C/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10054271	TCATAACTTGTAACT[C/T]GTTTGTAGCTTTAGT	2177
rs192262695	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10052022	AAGGGAAAGGTGGAG[G/T]TAAAGAATACCGAGA	2177
rs192333403	snp	G/T	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086627	GCTGGGATTACAGGC[G/T]CATGCTGACACACCC	2177
rs192339827	snp	C/T	0.0322114	0.122752	intron-variant	FANCD2	GRCh38.p7	3:10069677	CTGTGTTGGCCGGGC[C/T]GGTCTCCAGCTCCTA	2177
rs192341553	snp	A/G	0.00676609	0.0577691	intron-variant	FANCD2	GRCh38.p7	3:10033888	ATTTTTAGTAGAGAC[A/G]GAGTTTCACCGTGTT	2177
rs192467385	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10080972	AGAATACAGTCTTAG[A/G]TTAACAACTCATTTC	2177
rs192474989	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10066081	TCTTCACCAAGCACT[A/G]ACCCCCGTGTGCTTC	2177
rs192494494	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093459	GCCAGTTTAGGGAAG[A/G]CAATGGATGCATTTT	2177
rs192502709	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10030377	GCTGGGATATCGGAC[A/G]TGAGCCACCATGCCT	2177
rs192523376	snp	G/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10076742	TGTTTGTTTGTTTGT[G/T]GGAGACGGAGTCTTG	2177
rs192535505	snp	A/C	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10033288	TGCCTGTAGTCCCAG[A/C]TGCTTGGGCGCCTGA	2177
rs192558960	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10043308	TGTGAGTATGTATGT[A/G]TTTATATATTTTCTT	2177
rs192567847	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10060951	TGAGACATCAGGAGA[C/T]ATCTTTAGAATCCAC	2177
rs192591751	snp	A/C	0.02016	0.0983543	intron-variant	FANCD2	GRCh38.p7	3:10069194	TTCCTCTGCATAGCA[A/C]AGGAAACACCAAAGT	2177
rs192714437	snp	G/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10080800	AAGAAGGAGTCTATT[G/T]CCCTACATTTGTCAA	2177
rs192738435	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10046307	ATCTGCCCGCCTTGG[A/C]CTCCCAAAGTGCTGG	2177
rs192804303	snp	A/G	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10074224	CCTGGGATTACAGGC[A/G]TGAACCACCACACCT	2177
rs192808427	snp	A/G/T	0.00199481	0.0315187	intron-variant	FANCD2	GRCh38.p7	3:10045955	TGGCAACAAATACAC[A/G/T]CTGGAGTTGGCAAGT	2177
rs192825554	snp	A/T	0	0	intron-variant	FANCD2	GRCh38.p7	3:10050386	TCCCAGCACTTTGGG[A/T]GGCCAAGGCGGGCAA	2177
rs192827475	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10028173	AGAACCTGTACTTTT[A/G]TAGCACTTACATAAC	2177
rs192843638	snp	A/G	1.64732e-05	0.0028699	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085839	TCAACCTGAAAATCA[A/G]AATTTACTGTATTCA	2177
rs192938712	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10070753	GTAGAAAGAAGTAGA[C/T]ATGGGAGACTTTTCA	2177
rs192943703	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10030993	AGAAAATTTGAAACT[C/G]AAGAGGAATAATATA	2177
rs193013444	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10038480	ATATTTGGAAAAATG[A/T]TAATTGAGCCAACAT	2177
rs193031613	snp	C/T	0.00318978	0.0398085	intron-variant	FANCD2	GRCh38.p7	3:10074030	GGCTCACTGCAACCT[C/T]CACCTCCCGGGTTCA	2177
rs193212348	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10055673	AAAAATTAGCTGGAC[A/G]TGGTGGCAGGCGCCT	2177
rs193256104	snp	C/T	0.0482946	0.147699	intron-variant	FANCD2	GRCh38.p7	3:10070155	TCTGCCCGGCTGCCC[C/T]GTATGAGAAGTGAGG	2177
rs193257611	snp	A/G	0.00279162	0.0372561	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096946	TCCTAAGTGTCAGCT[A/G]GCTTGAGAAATAAAG	2177
rs193270710	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10034922	TCTGTTTTCCTCAGA[G/T]TTTAAACTAAGTTTA	2177
rs199509165	in-del	-/T			intron-variant	FANCD2	GRCh38.p7	3:10036699	TTTTTTTTTTTTTTT[-/T]AAGTATCTGTTGCTT	2177
rs199537747	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10073745	TCCCAATTATTTCTG[C/T]TGATCAGCCACCATT	2177
rs199541123	in-del	-/AA	0.0425829	0.139564	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082908	TTTGAACAATTTATC[-/AA]AGAGACTTATAGATG	2177
rs199545050	in-del	-/T			intron-variant	FANCD2	GRCh38.p7	3:10039422	CTTTTGGAGGTTGTA[-/T]TTTTTTTTTCTTTCT	2177
rs199563234	snp	A/C	3.40373e-05	0.00412523	missense	FANCD2	GRCh38.p7	3:10067255	CTGAGATGAAGGGGA[A/C]GGTGCTCACTCGGTT	2177
rs199616966	snp	A/T	0.00144863	0.0268741	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085786	TCCAGAAACTAAGCT[A/T]ACCCCTCTTACCTTG	2177
rs199662168	snp	A/C	0.000168922	0.00918871	intron-variant	FANCD2	GRCh38.p7	3:10062112	TACCCTAAAACTTAA[A/C]GTATAATAATAATTT	2177
rs199692792	in-del	-/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094703	TACTCTCAGAAATGA[-/T]TTTAAAAAAAAAAAA	2177
rs199714316	snp	C/G	3.30017e-05	0.00406199	intron-variant	FANCD2	GRCh38.p7	3:10073382	TGGAATGATGGGTAT[C/G]CGTGAAGGTTTGTGA	2177
rs199726231	snp	A/G	0.281043	0.248065	intron-variant	FANCD2	GRCh38.p7	3:10046558	AACTGTTTTTCTGTT[A/G]TTGCATATTTATTGA	2177
rs199789970	snp	C/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10073470	AAAATTAGGAAACAG[C/T]GAGCCAAAACTCTCT	2177
rs199898736	snp	C/G	1.64738e-05	0.00286995	missense	FANCD2	GRCh38.p7	3:10078168	AGTATGCTGACACCT[C/G]CTATTGCCAGGAGAG	2177
rs199989284	snp	A/T	0.00199794	0.0315432	intron-variant	FANCD2	GRCh38.p7	3:10074721	CTTCTTTCAGAAAGT[A/T]CCTCAGGTCTATTCT	2177
rs199996121	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086310	TTGTAGGAAGACCTT[A/G]TGTGGCTGAGGGGTA	2177
rs200013322	snp	C/T	3.30147e-05	0.00406279	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092279	GACTGCTTGACACAT[C/T]TCACCAAATAACTGC	2177
rs200041772	snp	C/T	1.64972e-05	0.00287199	synonymous-codon	FANCD2	GRCh38.p7	3:10060377	TATTGGTGCTGTGAC[C/T]ATGGCTGGCATCATG	2177
rs200073821	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10047815	GTTAAAATGAGAGCT[A/G]GGGAGGAGAAGTCTG	2177
rs200083185	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10073687	CATTTGTACTGTTCG[C/T]AGAATGAGTTTCATG	2177
rs200118565	snp	A/C/G	0.000593027	0.0172104	synonymous-codon	FANCD2	GRCh38.p7	3:10074640	TTGTGGACTTGTGAC[A/C/G]AAGTTCATCTTAGAT	2177
rs200170760	snp	A/C/T	4.95719e-05	0.00497834	intron-variant	FANCD2	GRCh38.p7	3:10034449	GAAACTGGTGACCAG[A/C/T]TCTTCTTTTTTCTGC	2177
rs200172687	snp	A/G	0.000346389	0.0131558	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10098977	CTTATATAATTTTTG[A/G]GACCCAGAAGAAACA	2177
rs200193941	snp	A/G			synonymous-codon	FANCD2	GRCh38.p7	3:10043139	AAAGTTGAAAAGTAA[A/G]GGACGAGCAAGGTAA	2177
rs200208121	snp	C/T	0.000388681	0.0139352	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087274	AAATTGGTGATGGGC[C/T]TAGATCCTTTTTTTT	2177
rs200211329	snp	A/T	5.00488e-05	0.00500219	intron-variant	FANCD2	GRCh38.p7	3:10049544	TTAGATATTGAATAC[A/T]ATAATTGGTGGGAGG	2177
rs200221245	snp	G/T	0.0679294	0.171319	intron-variant	FANCD2	GRCh38.p7	3:10046539	GCAAATGTACTGATT[G/T]GTTAACTGTTTTTCT	2177
rs200273431	snp	C/T			upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10026025	TGAGGTAGGCTGGGG[C/T]AGGGAGGGCGCTGAC	2177
rs200276130	in-del	-/GTATATAC			intron-variant	FANCD2	GRCh38.p7	3:10054428	TATACATATATACAT[-/GTATATAC]GTATATACATGTATA	2177
rs200335298	snp	C/T	7.88612e-05	0.00627889	missense	FANCD2	GRCh38.p7	3:10034776	CTTTTGTCTTGTGAG[C/T]GTCTGCAGGATGAGG	2177
rs200364254	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10048967	CTTGGAAACATGCAA[A/G]TCTAGCCTGTACTAT	2177
rs200380315	snp	G/T	3.29522e-05	0.00405894	missense	FANCD2	GRCh38.p7	3:10046665	TGCTAAGAAATAAGA[G/T]TCGATCAGGCTGCAT	2177
rs200471133	snp	C/T	1.64738e-05	0.00286995	missense	FANCD2	GRCh38.p7	3:10042562	TTTAATTTTTAGGTT[C/T]GCCAGTTGGTGATGG	2177
rs200473919	snp	A/T	0.00264419	0.0362643	intron-variant	FANCD2	GRCh38.p7	3:10052511	AGGTAAGAGGCAATA[A/T]GTTGGGAAAGATTTT	2177
rs200544843	snp	A/G	0.000136154	0.00824976	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095181	TTTCATAGAGCATTT[A/G]TAAACTTATTGGTTA	2177
rs200561665	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10060422	CACGTGGAGATTCTG[A/G]CTTCTGTGGTTTAAG	2177
rs200567617	snp	C/T	1.64833e-05	0.00287078	missense, downstream-variant-500B	FANCD2, FANCD2OS	GRCh38.p7	3:10081185	TTTTTCAACTGCTGA[C/T]CCCAATGTGTAACCA	2177
rs200568638	snp	C/G	0.000296492	0.012172	FANCD2	3	allele_origin=G(germline)/C(germline)	3:10078186	ATTGCCAGGAGAGTC[C/G]CCTTTCTCAAGGTTA	2177
rs200592206	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10073366	CAGCTAAACAAGGTA[C/T]TGGAATGATGGGTAT	2177
rs200595764	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10073474	TTAGGAAACAGCGAG[C/T]CAAAACTCTCTTAGG	2177
rs200631859	snp	C/G	0.000585289	0.0170968	missense	FANCD2	GRCh38.p7	3:10052484	AACAGAATGAAGCCA[C/G]CAGCCACATCCAGGT	2177
rs200664345	snp	G/T	8.24559e-05	0.00642037	intron-variant	FANCD2	GRCh38.p7	3:10047872	AGGTTGTGTACTAAC[G/T]GTTTCCTACAGCTTC	2177
rs200668378	snp	C/T	3.29701e-05	0.00406005	missense	FANCD2	GRCh38.p7	3:10036309	TTATCAAAACCTTAT[C/T]TGAGAAGTTGCCAGA	2177
rs200670011	in-del	-/AG			intron-variant	FANCD2	GRCh38.p7	3:10048494	ATTTTTAGTAGACAC[-/AG]CGTTTCACCATGTTG	2177
rs200677332	snp	A/C/G/T	0.000186873	0.00966469	intron-variant	FANCD2	GRCh38.p7	3:10074503	GAAGATTTATATATT[A/C/G/T]TCTTTGTTGCTGTGA	2177
rs200698016	snp	A/G	0.000198827	0.00996865	intron-variant	FANCD2	GRCh38.p7	3:10046569	TGTTGTTGCATATTT[A/G]TTGACAATAGGTGTT	2177
rs200732903	in-del	-/AC	0.124144	0.21601	intron-variant	FANCD2	GRCh38.p7	3:10054377	TATATACGTGTATAT[-/AC]ATATATATATGTATA	2177
rs200800132	snp	A/G	4.94222e-05	0.00497078	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087141	CCTTACAGCCAGAGC[A/G]TCCATTACTTGCAGA	2177
rs200805608	snp	C/T	0.00199792	0.0315431	synonymous-codon	FANCD2	GRCh38.p7	3:10049448	TGCCTTAGATGTCCT[C/T]CTAGAGTTGGTAGTG	2177
rs200836353	snp	A/G	0.00993419	0.0697739	intron-variant	FANCD2	GRCh38.p7	3:10033695	CTGCTATCAAAGCTA[A/G]GTCTTTTTTTTTTTT	2177
rs200848801	snp	A/G	4.94173e-05	0.00497053	synonymous-codon	FANCD2	GRCh38.p7	3:10065421	GCTGTGCCTGGCTCC[A/G]TATTTCCGGTTACTG	2177
rs200852630	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10045164	CTCTTTTTTTGTTTT[G/T]TTTTGTTTTTGTTTT	2177
rs200867320	snp	G/T	1.64741e-05	0.00286998	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092150	GTATTTGGCTGTGAC[G/T]CAGAGGTGCCCATAT	2177
rs200921782	snp	A/G	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10078253	TTGGGAACAAAGGAG[A/G]TATTATGATGAAAAA	2177
rs200971205	snp	C/G	0.000399281	0.0141238	missense	FANCD2	GRCh38.p7	3:10074615	ACATTGAGGTCTTCT[C/G]TATTCTACATTGTGG	2177
rs200973157	snp	G/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10071749	ATAATTAGATAGAAT[G/T]AATAAGATCTAGTTG	2177
rs200997373	snp	C/G	0.00199792	0.0315431	missense	FANCD2	GRCh38.p7	3:10062207	GCGATGAGCAGTGCA[C/G]ACAGGTGAGTTCTTT	2177
rs201022120	in-del	-/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083908	AAAAAAAAAAAAAAA[-/G]GTATGTCCACCAGGG	2177
rs201022435	snp	A/C			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098292	GAGTTTGAGTCCAAA[A/C]AGTCCCAAATCCAGA	2177
rs201040143	snp	C/T	0.000134823	0.00820935	intron-variant	FANCD2	GRCh38.p7	3:10060419	GTACACGTGGAGATT[C/T]TGACTTCTGTGGTTT	2177
rs201059067	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10054471	TATATATATATATAT[A/T]TATTTTTTTTTTTTT	2177
rs201076650	in-del	-/AGGTCAG			intron-variant	FANCD2	GRCh38.p7	3:10070373	CCCCGTCCGGGAGGG[-/AGGTCAG]GGGGTCAGCCCCCCG	2177
rs201078750	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10078241	GGCATAGTGGATTTG[A/G]GAACAAAGGAGGTAT	2177
rs201124351	snp	A/C/G	4.94208e-05	0.00497075	intron-variant	FANCD2	GRCh38.p7	3:10042671	CACTTGAGGTATGCT[A/C/G]TTATATCCCATCACA	2177
rs201131807	in-del	-/AAAAT	0.0154538	0.0865337	intron-variant	FANCD2	GRCh38.p7	3:10053535	AGTATAATAATAATA[-/AAAAT]AAAATAAAATAGAAT	2177
rs201177516	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10048985	TAGCCTGTACTATAT[A/G]GAGAAAACCTTTAAA	2177
rs201184977	snp	C/T	1.64735e-05	0.00286993	missense, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10081448	CTGCTGCAGATTTTT[C/T]ATGGGCTTTTTGCTT	2177
rs201201754	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10073720	TTTGAAATTGCCTGG[A/G]CCACATGGATCCCAA	2177
rs201243424	snp	G/T	0.000153988	0.00877328	missense	FANCD2	GRCh38.p7	3:10065395	TTTCTCCTTCTCAGA[G/T]TGGTGTCTCCGCTGT	2177
rs201287796	in-del	-/CG			intron-variant	FANCD2	GRCh38.p7	3:10054368	GTATATATATATATA[-/CG]TGTATATACATATAT	2177
rs201305493	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10078070	AACTAATCCTTTCCT[C/T]CATGTGACAGGCTAC	2177
rs201330931	snp	C/G	0.000398989	0.0141186	utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101294	TGCCTGCTTCTGTGT[C/G]TCTGCCAGCCTGTGA	2177
rs201353195	snp	A/G	1.64779e-05	0.00287031	intron-variant	FANCD2	GRCh38.p7	3:10039704	TGCTGCAGTTCTAAT[A/G]GTGTCTTCTACTGCA	2177
rs201387300	in-del	-/TA			intron-variant	FANCD2	GRCh38.p7	3:10035168	GATTTCTTTTTTTTT[-/TA]CAGTATGGGTGCATC	2177
rs201408009	snp	A/G	0.000677076	0.0183869	missense	FANCD2	GRCh38.p7	3:10060312	GACATGCACTTGGTG[A/G]TAAGAAAGCAGCTCT	2177
rs201487858	snp	C/T	0.00399202	0.044498	synonymous-codon	FANCD2	GRCh38.p7	3:10067265	GGGGAAGGTGCTCAC[C/T]CGGTTAAAGCACATT	2177
rs201500068	snp	A/G	1.711e-05	0.00292484	intron-variant	FANCD2	GRCh38.p7	3:10035154	CAAAGTGGAAAACAG[A/G]TTTCTTTTTTTTTTA	2177
rs201535479	in-del	-/AT	0.322721	0.23919	intron-variant	FANCD2	GRCh38.p7	3:10054437	TATACATGTATATAC[-/AT]GTATATACATATATA	2177
rs201540323	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10049020	TTAGCTCCTTGAGTG[C/G]CATCTTTTTGAGGAA	2177
rs201550150	snp	A/G/T	0.00163013	0.02851	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088779	GAGGAATCTGTAGTT[A/G/T]TATTCTACTTTGTTA	2177
rs201574604	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085390	TCTTTTTTCTTTTTT[C/T]TTTCTTTTTTTTTTT	2177
rs201623111	snp	C/T	3.29587e-05	0.00405934	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094371	AACACCGGGTAAGAG[C/T]TAAGAGCAGAGAACA	2177
rs201655331	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10073816	GTTTCATATTAATAC[C/T]ACATTTAATAAAGGA	2177
rs201719160	snp	A/G	0.00199481	0.0315187	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084498	AGACGGGGTTTCGCC[A/G]TGTTGCCCCCAGGCT	2177
rs201756450	snp	A/C			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090272	ATGGTGTGGGCACGC[A/C]TGCTTTTCCCGTCTT	2177
rs201770712	snp	A/G	0.276624	0.248578	intron-variant	FANCD2	GRCh38.p7	3:10046555	GTTAACTGTTTTTCT[A/G]TTGTTGCATATTTAT	2177
rs201810731	snp	A/G	0.00199798	0.0315436	intron-variant	FANCD2	GRCh38.p7	3:10049516	TAAAGGTATCTTATT[A/G]GCTTCTTGTACTTTA	2177
rs201811817	snp	A/G	0.000461779	0.015188	splice-donor-variant	FANCD2	GRCh38.p7	3:10073363	GGCCAGCTAAACAAG[A/G]TATTGGAATGATGGG	2177
rs201875004	snp	C/T	0.000115316	0.00759243	intron-variant	FANCD2	GRCh38.p7	3:10078203	CTTTCTCAAGGTTAG[C/T]GTAGGCAGAAGCATA	2177
rs201923921	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10073459	ACAAAGAAAAAAAAA[A/T]TAGGAAACAGCGAGC	2177
rs201937253	snp	A/G	4.94409e-05	0.00497172	intron-variant	FANCD2	GRCh38.p7	3:10042524	TGAGGTAGTGACATG[A/G]AAACCTATTAAGTTT	2177
rs201952387	snp	C/T			downstream-variant-500B, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10102138	CTTGATCTTGATCTT[C/T]TTTCCTTTTTTTTTT	2177
rs201967900	in-del	-/TATATGTATATACG			intron-variant	FANCD2	GRCh38.p7	3:10054384	GTGTATATACATATA[-/TATATGTATATACG]TATATGTATATACGT	2177
rs201998487	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085394	TTTTCTTTTTTCTTT[C/T]TTTTTTTTTTTTTTT	2177
rs202003085	snp	C/T	1.64743e-05	0.00287	synonymous-codon	FANCD2	GRCh38.p7	3:10041641	CCTACTGATAGAGAA[C/T]ACTTCACTCACTGTC	2177
rs202020623	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10046830	ACCCATTGAGATTTT[C/T]GAATTTTGTTTTTGC	2177
rs202028246	snp	C/T	0.00041196	0.0143461	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101202	GGATGGTGAAGAAGA[C/T]GAAGTAAGTGCTGGA	2177
rs202028914	snp	C/G	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10065808	AGCTCCAGAGGCAAC[C/G]TCCAGGTTTTATTGG	2177
rs202057202	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10076297	GTCTTTTTTTTTTTT[A/G]CCAAACCCTGTGTGT	2177
rs202096667	snp	G/T			upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10026008	CCAAGGTCACGGCGG[G/T]GTGAGGTAGGCTGGG	2177
rs202136353	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10029101	ATGCTATGTTAGTGA[C/T]GTGAAAGGAAAAATA	2177
rs202196826	snp	A/G	0.000399281	0.0141238	missense	FANCD2	GRCh38.p7	3:10034717	AAGAATTTGTTAGTG[A/G]CCTGGAGTCTTACAT	2177
rs202213490	in-del	-/TTCTTTT			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085374	TACTTTCCATTTCAA[-/TTCTTTT]TTCTTTTTTCTTTCT	2177
rs367547321	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10046295	CCTGACCTTGTGATC[C/T]GCCCGCCTTGGCCTC	2177
rs367549918	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10048333	TTTGAGACGTGGTTT[C/T]GCTCTTCATGCCCAG	2177
rs367551904	snp	C/T	0.000115828	0.00760924	synonymous-codon	FANCD2	GRCh38.p7	3:10062193	GAGAGCCAACCTGAG[C/T]GATGAGCAGTGCACA	2177
rs367552677	snp	A/G	1.64727e-05	0.00286986	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088913	CTGATCAACTCTCCT[A/G]AAGATGCATCTTCCT	2177
rs367559791	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10028170	CATAGAACCTGTACT[C/T]TTATAGCACTTACAT	2177
rs367562418	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10055640	ACACGGTGAAACCCC[A/G]TCTTTACTAAAAATA	2177
rs367569596	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10041969	AGTGGTGCAATCTCC[A/G]CTAACTGCAACCTCT	2177
rs367622996	snp	A/G	8.70299e-05	0.00659601	intron-variant	FANCD2	GRCh38.p7	3:10043442	TGTAAGTTCTTTTCT[A/G]GTACGTAGAAGAGTA	2177
rs367736998	snp	A/G	4.94214e-05	0.00497074	missense	FANCD2	GRCh38.p7	3:10047960	TGTCGCTGGCTCAGA[A/G]TTTGCTTCACTCTCT	2177
rs367751672	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10052823	CAAATCAAAACCACA[A/G]TGAGATACCATCTCA	2177
rs367816407	snp	A/G	3.29516e-05	0.00405891	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10081471	TTTTGCTTGGTAAGT[A/G]TGTGGGAAGTGTGGA	2177
rs367824549	snp	A/G	3.30191e-05	0.00406306	missense	FANCD2	GRCh38.p7	3:10043069	TTTCTGAGCTTCGGG[A/G]GAAGTTGGATCTGCA	2177
rs367838566	snp	C/T	1.68218e-05	0.00290011	synonymous-codon	FANCD2	GRCh38.p7	3:10072962	TATTTCAGCAAAAAT[C/T]AGAAAGAAAGGAAAA	2177
rs367856025	snp	C/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086929	CATCAGTGGGGCTGT[C/G]TTCTGCCCTGGCTTT	2177
rs367882112	snp	C/T	1.64795e-05	0.00287045	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098794	CATGTCATCCCAGGC[C/T]TCCAAGAGCAAAGCC	2177
rs367894991	snp	A/G	0.000153988	0.00877328	intron-variant	FANCD2	GRCh38.p7	3:10049533	CTTCTTGTACTTTAG[A/G]TATTGAATACTATAA	2177
rs367949626	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095968	CTCACTGCAAGTTCC[A/G]CCTCCCGGCTGGACA	2177
rs367976708	snp	C/G	0.000153988	0.00877328	splice-acceptor-variant, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096325	ATTTATTTCCATTCA[C/G]ATTCACCAGGACACG	2177
rs367980494	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10038054	AGAGTACAGTGGTGC[A/G]ATCTTGGCTCACTGC	2177
rs367988817	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10070405	CCCCGCCCGGCCAGC[C/T]GCCCCGTCCGGGAGG	2177
rs367989108	snp	C/T	0.000153988	0.00877328	intron-variant	FANCD2	GRCh38.p7	3:10067168	AACAAGGTTAAAATC[C/T]GAACATTTGGAAGTA	2177
rs367989815	snp	C/T	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10043719	GATAGCTGATGGTTG[C/T]CAGATGGACACATTG	2177
rs367991967	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10048308	CATGAGACACTTTTT[G/T]TTGTTTTGTTTTGAG	2177
rs367997565	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10077418	AAATTAGTCAGGCAT[A/G]GTGGTGGGCACCTGT	2177
rs368019809	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10047700	TGGATAATAATTGAC[C/T]TTTAAGCTCAAAGAA	2177
rs368066716	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10047709	CTTAAAAGTCAATTA[A/T]TATCCAAACGTGGAA	2177
rs368099170	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10052581	GGAGTGCAGTTGGCA[C/T]GATCTCAGCTCATTG	2177
rs368121256	snp	A/G	6.60295e-05	0.00574547	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085958	CAAGATTGTTGTCCC[A/G]AGAAACTCCTAGGAA	2177
rs368124145	snp	A/G			intron-variant, downstream-variant-500B	FANCD2, FANCD2OS	GRCh38.p7	3:10099941	TGGCTCACACCTGTA[A/G]TCGTAGCACTTTGTG	2177
rs368195150	snp	C/T	1.64762e-05	0.00287016	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096461	GGCAATCTAAAAAAC[C/T]GGGACTTGCAGGTAA	2177
rs368201679	snp	A/G	0.000134483	0.00819899	intron-variant	FANCD2	GRCh38.p7	3:10072827	AAGTCTAATGGTGGT[A/G]TGTAATTGGTACACA	2177
rs368249182	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10062049	GGGTGCAGCACACCA[A/G]CATGGCACATGTATA	2177
rs368257371	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10047664	GCAGATAGGAATGTT[C/G]TATTAGGCTTGTAAT	2177
rs368272136	snp	C/T	0.00199481	0.0315187	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096003	ATGTTTAAGGAATTC[C/T]CTTAGCTAAACAGGG	2177
rs368283092	snp	A/G	0.000437904	0.0147905	intron-variant	FANCD2	GRCh38.p7	3:10039226	GTATTAATGCTTGCT[A/G]TTATTTTGACCAGAA	2177
rs368329620	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10078826	AAAAGAACTAGCCGG[G/T]CATGGTGGTGCAGCT	2177
rs368361816	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10031636	TTATTTCTTTTTATG[G/T]GTTGAAAGTCTTGGG	2177
rs368366938	snp	C/G/T	6.68532e-05	0.00578124	intron-variant	FANCD2	GRCh38.p7	3:10032803	TCCTTTACTATTTGC[C/G/T]ATATTCTTGAAAATT	2177
rs368403335	snp	G/T	0.00358779	0.0422022	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091458	ACCTGGATGTCAGAC[G/T]CAGACCCTGTCTCAA	2177
rs368441247	snp	A/T	0.000247078	0.0111121	synonymous-codon	FANCD2	GRCh38.p7	3:10047955	CATTCTGTCGCTGGC[A/T]CAGAGTTTGCTTCAC	2177
rs368448399	snp	A/G	3.30235e-05	0.00406333	intron-variant	FANCD2	GRCh38.p7	3:10034465	TCTTCTTTTTTCTGC[A/G]TAGCTGTGGATCAAA	2177
rs368471033	snp	C/G	1.68278e-05	0.00290062	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090267	GCATCATGGTGTGGG[C/G]ACGCATGCTTTTCCC	2177
rs368501428	snp	A/T	1.68303e-05	0.00290084	missense	FANCD2	GRCh38.p7	3:10039350	TTGACAGAGTTGTGG[A/T]TGGCAAGGTAGGCTT	2177
rs368551193	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10056275	TGAATAATGTTGCTG[C/T]GACCATTGGTTTACA	2177
rs368576184	snp	G/T	0.0130921	0.0798413	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090960	GCTAACTGGCATGAG[G/T]TAAGCCAGCCTGTTT	2177
rs368616535	snp	C/T			intron-variant, utr-variant-5-prime, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026513	AGTCTCTCGAGGCCC[C/T]GCTCCCCTGCGGCCT	2177
rs368626460	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10046927	ATTTAAGTAGCTTAT[A/G]AAAACCTTGAGGGGA	2177
rs368684162	snp	C/T	0.000153988	0.00877328	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090376	TGGCACAGCAGCAGA[C/T]TCGCAGCAGGTGAGT	2177
rs368688112	snp	C/G	0.000280013	0.0118291	intron-variant	FANCD2	GRCh38.p7	3:10064712	CTGCAACATCAGATT[C/G]TGGTTTTTCTCCGCA	2177
rs368763625	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10076316	AACCCTGTGTGTGGC[A/T]TTCAAAGTCATTTTT	2177
rs368812039	snp	A/T	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10040910	TAGCATCTGTCACCG[A/T]CTGTTGGGCGCAGTG	2177
rs368822243	snp	C/T	3.30014e-05	0.00406197	intron-variant	FANCD2	GRCh38.p7	3:10041594	GTTCAAACCATTATA[C/T]AACTTTTTTCTTTTT	2177
rs368848371	snp	C/T	1.64751e-05	0.00287007	stop-gained	FANCD2	GRCh38.p7	3:10035231	GGGATTGACATACTG[C/T]AGGTAAGACTGTCAC	2177
rs368885711	snp	C/T	0.000153988	0.00877328	missense	FANCD2	GRCh38.p7	3:10065443	CGGTTACTGAGACTT[C/T]GTGTGGAGAGACAGC	2177
rs368886461	snp	A/C	4.9436e-05	0.00497148	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101227	GCTGGAGAAAAGGAG[A/C]AAGATAGTGATGAGA	2177
rs368904137	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10048283	GATCCAGATCTAGTC[C/G]ATTTCAAAACATGAG	2177
rs368933481	in-del	-/ATG			intron-variant	FANCD2	GRCh38.p7	3:10071947	GTACTTTTGGTGCAG[-/ATG]GGGTTTCACCGTGTT	2177
rs368952542	in-del	-/T			utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101376	ATCCTTTTTTGTTCC[-/T]CTTTTTTTTTTTTTT	2177
rs368995969	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10079112	AGCCAGGTATGGTGG[C/T]GCATGCTTGTAGTCC	2177
rs368999017	snp	A/G	0.000153988	0.00877328	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090390	ACTCGCAGCAGGTGA[A/G]TAAGATAATAGTCAC	2177
rs369022159	snp	C/T	3.29465e-05	0.00405859	stop-gained, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088463	GCTTCCCTTGCCAGA[C/T]AATTCCTCTGTCGGG	2177
rs369049338	snp	A/C	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10024869	GATGAATTTCTTTTG[A/C]TTACACTGCCTGGAA	2177
rs369070813	snp	G/T	0.000153988	0.00877328	missense	FANCD2	GRCh38.p7	3:10043829	CTCCTGTTTTTTCAG[G/T]CAATTGAAAACACTG	2177
rs369114739	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10038559	TTGACTTTCTATGTT[C/G]CCTTAGCAATATATG	2177
rs369164193	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10054427	TATATACATATATAC[A/G]TGTATATACATGTAT	2177
rs369180295	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10071185	TATCCAAAGGACAGG[C/T]AATAACAGATGCTGG	2177
rs369195246	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10073843	AGGAGGAAACTAAGA[C/T]CCAGGGAGGGCAAGT	2177
rs369205123	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10079564	CCACCTCGGCCTCCC[A/C]ATCCGCCCACCTCGG	2177
rs369241246	snp	G/T	1.65244e-05	0.00287436	missense	FANCD2	GRCh38.p7	3:10074544	GGAGTTCACAGGGAA[G/T]GAAGAAAAGACATCA	2177
rs369242410	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10053786	CAAAAAGCTTTGTCT[A/G]TTAGGGTAGAGATGG	2177
rs369245523	multinucleotide-polymorphism	CA/TG			intron-variant	FANCD2	GRCh38.p7	3:10042191	TTGAGCCACCGTGCC[CA/TG]GCCCACAGGTCTGTT	2177
rs369295785	in-del	-/T			intron-variant	FANCD2	GRCh38.p7	3:10037010	CAGCTAATTTTCGTG[-/T]GTTTTTTTTTTTTTG	2177
rs369357413	snp	G/T	0.00119737	0.0244387	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097330	TCTTCCTAATAAGCC[G/T]GGGAGCGCTATAGGA	2177
rs369364109	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10070073	GCGCCTCTGCCCCAC[C/T]GCCCCGTCTGGGATG	2177
rs369404910	snp	C/T	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10057596	TCTCAATCTCTTAAC[C/T]TCATGATCTGCCTGT	2177
rs369405673	snp	A/G	4.94222e-05	0.00497078	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087204	GCTCTTTATCTCATC[A/G]GACTTTTGATGGTTA	2177
rs369411085	snp	A/G	1.64803e-05	0.00287052	intron-variant	FANCD2	GRCh38.p7	3:10042521	AGTTGAGGTAGTGAC[A/G]TGAAAACCTATTAAG	2177
rs369470214	in-del	-/T			intron-variant	FANCD2	GRCh38.p7	3:10063978	TACACTCTTCAAGTC[-/T]TTCTGTTGCAGTGTG	2177
rs369504431	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10047743	CATTGATGCTGAGAG[A/T]AATCTCAGAATGATG	2177
rs369536972	snp	A/G	0.00199481	0.0315187	intron-variant	FANCD2	GRCh38.p7	3:10069634	GCCTGACTGGTTTTC[A/G]TACTTTTTTGGTGGA	2177
rs369541967	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10071899	TGAGTAGCCGGGACT[A/G]GAAGTGTGCACCACC	2177
rs369598129	snp	A/C/G	0.00239393	0.0345281	intron-variant	FANCD2	GRCh38.p7	3:10051119	GGCGCGGTGGCTCAC[A/C/G]CCTGTAATCCCAGCA	2177
rs369640359	snp	A/G	0.000153988	0.00877328	missense	FANCD2	GRCh38.p7	3:10060363	AAGCTCATTGGGATT[A/G]TTGGTGCTGTGACCA	2177
rs369702202	snp	G/T	0.000494715	0.0157198	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093268	CAGCCTTGGTTTCTT[G/T]TCTTTCACCTCTCCA	2177
rs369736809	snp	A/C	1.64798e-05	0.00287047	intron-variant	FANCD2	GRCh38.p7	3:10063772	CCCAAGGTTTAAACC[A/C]TTCTTCCTCTTTGCT	2177
rs369737008	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10052720	AAAGTGGGCGAAGGA[C/T]ATGAACAGACACTTC	2177
rs369743385	snp	C/T	0.000181571	0.0095264	intron-variant	FANCD2	GRCh38.p7	3:10034833	AATCTTGCTGAAATT[C/T]AGTCTGTTTTGCCAA	2177
rs369761534	snp	A/G	0.000193981	0.00984647	intron-variant	FANCD2	GRCh38.p7	3:10043777	TGAATAAGGTGTAAC[A/G]TGTTTCGCTGATGTG	2177
rs369777245	snp	A/T	5.09092e-05	0.005045	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088584	GCCAAATAGCTTTTT[A/T]CTATTTTGCTACTGT	2177
rs369787164	in-del	-/CAA			intron-variant	FANCD2	GRCh38.p7	3:10069048	TACTAACAACAACAA[-/CAA]AAAACATTCAGAAAA	2177
rs369796065	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10075953	AGCCAGGATGGTCTC[C/G]ATCTCCTGACCTCGT	2177
rs369823368	in-del	-/AGTA			intron-variant	FANCD2	GRCh38.p7	3:10046723	CTCTGTTCATTACTT[-/AGTA]AGTGTCAGAGACTAT	2177
rs369844298	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083425	GACTTAGCATGCCAA[A/G]TGTTGGTGAGAAGGT	2177
rs369870102	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10057657	CATGAGCTACTGCTC[C/G]CGGCCTCCATTAAGT	2177
rs369872417	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10073980	AGATGGAGTCTCACT[C/T]TGTCACCCAGGCTGG	2177
rs369875109	in-del	-/G			utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101371	GTAGGATCCTTTTTT[-/G]TTCCTCTTTTTTTTT	2177
rs369883803	snp	C/T	1.64746e-05	0.00287002	synonymous-codon	FANCD2	GRCh38.p7	3:10064373	ATGGGTTGGGCATAC[C/T]ATCTGTAATGATTTC	2177
rs369890094	snp	A/G	6.60142e-05	0.0057448	intron-variant	FANCD2	GRCh38.p7	3:10039864	GATAAACCCTCTGTC[A/G]TCATCTAAGTGAGGC	2177
rs369910721	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10047730	AAACGTGGAATCCCA[C/T]TGATGCTGAGAGTAA	2177
rs369935595	snp	A/G	1.64754e-05	0.00287009	synonymous-codon	FANCD2	GRCh38.p7	3:10039810	ACCTGAGATCCTAGG[A/G]GATTCCCAGCACGCT	2177
rs369962711	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10070818	GGGATCCTGTTGATC[G/T]GTGACCTTACCCCCA	2177
rs370024653	snp	C/G	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10064057	TTTCTGCCCTACCCT[C/G]TCTCACGGCTCTTCT	2177
rs370041054	snp	A/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097010	GGGCGTCCGGGGGAG[A/T]CATCACACGTTGATA	2177
rs370043861	snp	A/G	1.67416e-05	0.00289318	intron-variant	FANCD2	GRCh38.p7	3:10035123	AAAGATGATAAAAGC[A/G]TTAAAACAAGGAAAG	2177
rs370078641	snp	C/T	0.000184349	0.00959898	synonymous-codon	FANCD2	GRCh38.p7	3:10043846	AATTGAAAACACTGC[C/T]TCAGTATCTGAACAC	2177
rs370168719	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10048278	ATTAAGATCCAGATC[C/T]AGTCCATTTCAAAAC	2177
rs370172046	snp	C/T	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10072523	ACCTCAGGTGATCCG[C/T]GCGCCTTGACCTCCC	2177
rs370173134	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10061269	CTTGCAACGTACTTT[A/T]ATACTTTCTCTAAGA	2177
rs370173340	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10065744	TATTTTAATCAGATC[G/T]TGGCCTTCAAATATG	2177
rs370202671	snp	A/G	1.66385e-05	0.00288426	missense	FANCD2	GRCh38.p7	3:10065950	TTCATGTGTTCTCTC[A/G]TATTTCTTACTCTCA	2177
rs370219244	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10078642	TACGGGCATGAGCCA[C/T]CGCGCCCGGCCTCAT	2177
rs370232992	snp	A/C/T	8.26666e-05	0.00642866	intron-variant	FANCD2	GRCh38.p7	3:10036348	TTGAAAAGTAAGTGG[A/C/T]GTTATTATGGAATGT	2177
rs370270635	snp	C/T	0.0113291	0.0744057	intron-variant	FANCD2	GRCh38.p7	3:10079249	ACTCTGTCTCAGAAA[C/T]AAAAAAAAAAAAATA	2177
rs370284275	snp	A/G	6.61912e-05	0.0057525	synonymous-codon	FANCD2	GRCh38.p7	3:10060395	GGCTGGCATCATGGC[A/G]GCAGACAGGTACACG	2177
rs370316786	snp	A/G	1.65345e-05	0.00287524	missense	FANCD2	GRCh38.p7	3:10032934	TTCTTAAGATATCAG[A/G]AATTATTCTTAAAAC	2177
rs370333100	in-del	-/G			intron-variant	FANCD2	GRCh38.p7	3:10037131	ATGTGGCCCTACCTG[-/G]TTTTTTTTTAATTAC	2177
rs370343891	snp	A/G	1.64925e-05	0.00287158	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096334	CATTCAGATTCACCA[A/G]GACACGAGACTCACC	2177
rs370370618	snp	A/G	0.00358779	0.0422022	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090529	CAGTGGCATGATCTC[A/G]GCTCACTGCAACCTC	2177
rs370388163	in-del	-/AAGGGTATCTTG	0.00159617	0.0282053	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095132	GGAGCTTTTGATTGC[-/AAGGGTATCTTG]AATCTAAAATGAAAT	2177
rs370391996	snp	A/G	1.71569e-05	0.00292885	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095279	GGCATTCCAAGGTAA[A/G]AAGGGGAGCAGGTTC	2177
rs370401475	snp	C/T	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10040120	GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAC	2177
rs370404406	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10055534	AATTCCATTCTTGGC[C/T]GGGCACGGTGACTCA	2177
rs370455670	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10039951	TTCTATCTAAAAAGA[A/G]GATGATACCCCCCTT	2177
rs370459744	snp	C/T	1.65364e-05	0.0028754	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10098994	ACCCAGAAGAAACAA[C/T]GACACAATCTTAGAA	2177
rs370522983	snp	A/G	4.94287e-05	0.00497111	missense	FANCD2	GRCh38.p7	3:10046668	TAAGAAATAAGATTC[A/G]ATCAGGCTGCATTCA	2177
rs370531941	snp	A/G/T	1.64803e-05	0.00287052	intron-variant	FANCD2	GRCh38.p7	3:10078031	AGAAAAAAAATTATC[A/G/T]TGAAATGACTAGGAC	2177
rs370534137	snp	C/T	3.29571e-05	0.00405924	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088999	AGATAGAATCATCAT[C/T]AGGCTGGGCACGGTG	2177
rs370543217	in-del	-/AT			intron-variant	FANCD2	GRCh38.p7	3:10030096	CTGGCCCATTATATC[-/AT]TTTTTTTTTTTTTTT	2177
rs370546202	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10089857	CAATAGTTATCTTAA[C/T]ATTTGTAGTCTTTTC	2177
rs370554100	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10072760	TATAAGCATTCAGCC[A/G]TGCTTGGTAATTTTG	2177
rs370570694	snp	C/T	0.000437904	0.0147905	intron-variant	FANCD2	GRCh38.p7	3:10079816	GGGGAAGCAGTTGGA[C/T]GGTACATATAACAAA	2177
rs370587913	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10046893	TTTGCAACTTTGACA[A/C]ACTGGCCTTCCGTAT	2177
rs370594732	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10060201	TTAGTAAACGGTAAA[C/T]GCCTTTATAGTCTAG	2177
rs370624437	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10046215	CATGCTGCCACACCC[A/G]GCTAATTTTTTGTAT	2177
rs370636147	in-del	-/CT	0.00358779	0.0422022	intron-variant	FANCD2	GRCh38.p7	3:10041931	TGAGACGGAGTATCA[-/CT]CTGTCACCCAGGCTG	2177
rs370641152	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10072104	TGACTACAGTCAACA[A/G]TAACTTACTGTACAT	2177
rs370641659	snp	C/G/T	0.000148682	0.00862092	synonymous-codon, missense	FANCD2	GRCh38.p7	3:10043128	GCTTCCCAAGTAAAG[C/G/T]TGAAAAGTAAAGGAC	2177
rs370704605	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10048286	CCAGATCTAGTCCAT[G/T]TCAAAACATGAGACA	2177
rs370765663	snp	C/T	0.000226105	0.0106302	intron-variant	FANCD2	GRCh38.p7	3:10039379	TTATGGACTTTATCT[C/T]TTGAATTTAAAGAGT	2177
rs370780571	multinucleotide-polymorphism	CA/CT/TG			intron-variant	FANCD2	GRCh38.p7	3:10031319	CCATCTTGGCTAACA[CA/CT/TG]GTGAAACCCCGTCTC	2177
rs370815069	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10055238	TTAAGTATATTCACA[A/G]TGTTATACAACCATT	2177
rs370823379	snp	C/T	0.00199481	0.0315187	intron-variant	FANCD2	GRCh38.p7	3:10075164	AAATAGCTAGCAATA[C/T]GGTAGCTTTATTATT	2177
rs370843473	snp	A/G	1.64996e-05	0.0028722	utr-variant-5-prime	FANCD2	GRCh38.p7	3:10028646	ATTTAAGTGCACAAG[A/G]CATTGGTCAAAATGG	2177
rs370845109	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10061959	GGAACATCACACACC[A/G]GGGAATGTTGTGGGG	2177
rs370845201	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10047770	GATGAAGGATTATTT[C/T]TGTGTAAAACAAAGA	2177
rs370870556	snp	C/T			downstream-variant-500B, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10102124	TTCTGGAGGATTGAC[C/T]TGATCTTGATCTTCT	2177
rs370937444	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10048535	GTCTCGAACTCCTGA[C/T]CTCAGGTGAACCGCC	2177
rs370942558	snp	C/T	0.00159617	0.0282053	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085460	GCAGTGGCACAATCT[C/T]GGCTCACTGCAGCCT	2177
rs370944916	snp	C/T	0.000153988	0.00877328	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088516	GAAGAGCAACATCTC[C/T]AATGACCAGCTCCAT	2177
rs370954429	snp	C/T	3.48876e-05	0.00417643	intron-variant	FANCD2	GRCh38.p7	3:10043884	TGTTCATGTACTATG[C/T]ATTTTCAGTATTGCA	2177
rs370987400	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10051298	AGGCAGGAGAATGGC[A/G]TGAACCCAGGAGGCG	2177
rs371002110	snp	C/G	0.00159617	0.0282053	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084549	AAGTGATCCACCCGC[C/G]TCAGCCTCCCAAAGT	2177
rs371005906	snp	C/T	0.031825	0.122064	intron-variant	FANCD2	GRCh38.p7	3:10070360	GCCAGGCCAGCCGCC[C/T]CGTCCGGGAGGGAGG	2177
rs371043591	in-del	-/G			intron-variant	FANCD2	GRCh38.p7	3:10048318	TTTTTTTGTTTTGTT[-/G]TTGAGACGTGGTTTT	2177
rs371097813	snp	A/C	0.000437904	0.0147905	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092121	TATATCTTAGTGGGA[A/C]TACAGTAAGGGAAGT	2177
rs371116586	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10024899	AAAGTCTTGAATTAT[C/T]GTAGACTGAACAAGT	2177
rs371150775	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10047660	TTGAGCAGATAGGAA[C/T]GTTCTATTAGGCTTG	2177
rs371167683	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10051472	GAAGATGGAGGCAGA[C/G]GCTATTGGCTTTGGC	2177
rs371177585	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10066758	GAGACAGAGTCTTGC[C/T]CTGTCACCCAGGCTG	2177
rs371246379	snp	A/C	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10040930	TGGGCGCAGTGGCTC[A/C]TGCCTTTAATCCCAG	2177
rs371258999	snp	A/G	0.000560335	0.0167288	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081306	AGGAAAATGAGGACA[A/G]TTACTGAAGCAACTG	2177
rs371273577	snp	A/G	1.64735e-05	0.00286993	missense	FANCD2	GRCh38.p7	3:10042640	TTCATTCTTCATTCC[A/G]TAACAGCCATGGATA	2177
rs371277421	snp	C/G	1.64814e-05	0.00287061	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094380	TAAGAGCTAAGAGCA[C/G]AGAACAAAGATATGC	2177
rs371284570	snp	A/G/T	3.29496e-05	0.00405881	missense	FANCD2	GRCh38.p7	3:10041637	GTGACCTACTGATAG[A/G/T]GAATACTTCACTCAC	2177
rs371299677	snp	A/G	0.000437904	0.0147905	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093230	AGCGGGAAAGAGGCT[A/G]GAGTGCTCAAAGGAG	2177
rs371321981	in-del	-/T/TT/TTT/TTTT	0.585762	0.215041	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087281	GATGGGCCTAGATCC[-/T/TT/TTT/TTTT]TTTTTTTTTTTTTTT	2177
rs371358308	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10041921	TTTTTTTTTTTGAGA[C/T]GGAGTATCACTCTGT	2177
rs371395855	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10034579	CTTGTGCCAGCATAA[C/T]TCTAGAATTTGGAAT	2177
rs371415551	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10065340	ATATCTCCCTATGTA[C/T]GTGGAGTAATACACC	2177
rs371451683	snp	C/G/T	1.65671e-05	0.00287807	missense	FANCD2	GRCh38.p7	3:10032846	GAAACCAGGAAGCAA[C/G/T]CACTTTCCAAAAAGA	2177
rs371463731	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10043002	ACTGGACTGTGCCTA[C/T]CCACTATGAATGAGC	2177
rs371559678	snp	C/T	1.64765e-05	0.00287019	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10081474	TGCTTGGTAAGTATG[C/T]GGGAAGTGTGGAGAG	2177
rs371563130	snp	G/T	0.000109997	0.00741528	intron-variant	FANCD2	GRCh38.p7	3:10065814	AGAGGCAACCTCCAG[G/T]TTTTATTGGCTTGCA	2177
rs371564243	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10056450	CCAACAATGTATGTA[G/T]GTTCCAATTTCTCCA	2177
rs371571394	snp	C/T	0.00159617	0.0282053	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088687	ACAATTTGGAACATG[C/T]GGATCTTAAGATCCT	2177
rs371577566	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10047718	CAATTATTATCCAAA[C/T]GTGGAATCCCATTGA	2177
rs371581727	snp	C/T	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10049642	AATTCATTCAGCAAA[C/T]ACTTCTTTATACCTA	2177
rs371590669	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10079800	CGTGCACCTAGCATC[C/T]GGGGAAGCAGTTGGA	2177
rs371615297	snp	A/G	0.000153988	0.00877328	intron-variant	FANCD2	GRCh38.p7	3:10036238	GGATTATACATTTCT[A/G]TTGTGTATTTTGAGA	2177
rs371618992	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082589	AATTAATTTGAGCAC[C/T]CTATATAGCTTTTAC	2177
rs371634866	snp	A/G/T			intron-variant, downstream-variant-500B	FANCD2, FANCD2OS	GRCh38.p7	3:10100127	CAGGAGGTGGAGGCT[A/G/T]CAGTGAGCCATCATC	2177
rs371635259	snp	G/T	1.64798e-05	0.00287047	intron-variant	FANCD2	GRCh38.p7	3:10039678	GTAGTCTTTCTTTAT[G/T]CTGGGTAATGTGCTG	2177
rs371651879	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090521	CTGGAGTGCAGTGGC[A/G]TGATCTCGGCTCACT	2177
rs371700840	snp	A/T	8.30268e-05	0.00644256	intron-variant	FANCD2	GRCh38.p7	3:10028773	GCAATGTGTGAGGCA[A/T]GTGAGAGATATAAAG	2177
rs371712973	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10052713	CCATCAAAAAGTGGG[C/T]GAAGGACATGAACAG	2177
rs371723938	snp	A/G	2.01566e-05	0.00317457	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087315	TAATGAATAGGACTA[A/G]TATCTCACACTTACA	2177
rs371726359	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10075332	GGGGCTATAGGCATC[C/T]GCCATCACACCCGGC	2177
rs371731073	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10048340	CGTGGTTTTGCTCTT[C/G]ATGCCCAGGCTGGAG	2177
rs371741197	snp	C/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093795	AATGCTACTTCGCCA[C/G]TCCTCAAGTTTCCTT	2177
rs371757266	snp	A/G	3.29527e-05	0.00405898	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098810	TCCAAGAGCAAAGCC[A/G]CTGAGGTATCTCTAC	2177
rs371794183	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10070439	GGGGCGCCTCTGCCC[A/G]GCCGCCCCTACTGGG	2177
rs371809637	in-del	-/GAGCG			intron-variant	FANCD2	GRCh38.p7	3:10047485	ATTATTGGTAGGTTA[-/GAGCG]TGATCACTTCTCTTC	2177
rs371851839	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10047627	TGGGATTTAGAACAT[C/G]TGGCCTCCAATCCCA	2177
rs371890961	snp	A/G	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10031406	TACTGGGAGGCTGAG[A/G]CAGGAGAATGGCATG	2177
rs371903403	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10053753	TGCCAGGCACTGATA[C/T]ATTAGATCCTCTGCC	2177
rs371912466	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10070838	CCTTACCCCCAACCC[C/T]GTGCTCTCTGAAACA	2177
rs371915501	snp	C/T	0.000230867	0.0107415	synonymous-codon	FANCD2	GRCh38.p7	3:10034509	GAAGCTCTTTCAGAC[C/T]CTGAGGAGACACCCT	2177
rs371928644	snp	C/T	0.00060943	0.0174454	synonymous-codon	FANCD2	GRCh38.p7	3:10039822	AGGGGATTCCCAGCA[C/T]GCTGATGTGGGGAAA	2177
rs371961988	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10067729	CTTGAACCTGGGAGG[C/T]GGAGGTTGCAGTGAG	2177
rs371985200	snp	A/G	0.000307953	0.0124049	intron-variant	FANCD2	GRCh38.p7	3:10043638	AGGAAATGAGTGGCA[A/G]TTAGTGACAGATGTA	2177
rs371997090	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091194	CAGATGATCCTCCCA[C/T]GTCAGCCTCCCAAAT	2177
rs372012199	snp	A/G	0.00199481	0.0315187	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096082	GGTAAATTCATTGAA[A/G]ATCGGCCAGTAAGAG	2177
rs372015176	snp	A/G	3.30704e-05	0.00406622	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085969	TCCCAAGAAACTCCT[A/G]GGAACAGGATTGGCA	2177
rs372087941	snp	A/G	0.000153988	0.00877328	synonymous-codon	FANCD2	GRCh38.p7	3:10062199	CAACCTGAGCGATGA[A/G]CAGTGCACACAGGTG	2177
rs372138157	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10044205	AGGTCCCTGTATCTG[C/T]CTAATTGCCCTTCCT	2177
rs372151573	snp	A/G	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10038212	GGCCAGGCTGGCCTC[A/G]AACTCCTGACCTCAA	2177
rs372172170	snp	C/G	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10062602	TTGCTTCTAGTCACT[C/G]TCAGTTCACCAGAAA	2177
rs372202221	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10052732	GGACATGAACAGACA[C/T]TTCTCAAAAGAAGAC	2177
rs372212788	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10048327	TTTTGTTTTGAGACG[G/T]GGTTTTGCTCTTCAT	2177
rs372215382	snp	A/G	0.000264127	0.0114888	synonymous-codon	FANCD2	GRCh38.p7	3:10064849	AAAAGATGGGGGTCC[A/G]GTGACCTCACAGGAA	2177
rs372245181	in-del	-/AGTT			intron-variant	FANCD2	GRCh38.p7	3:10075252	AGTGGCGCGGATCTC[-/AGTT]CACTCACTGCAAGCT	2177
rs372325512	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10056040	CGCACCACCACTCCC[A/G]GCTGATTTTTGTATT	2177
rs372336739	snp	G/T	0.0329836	0.124112	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091117	ACAGGGTCTGAGTCT[G/T]ACATCCAGGTTGGAG	2177
rs372352101	snp	A/G	0.00119737	0.0244387	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100984	TGAGGCAGGGGAATC[A/G]CTTGAACCCGGGAGG	2177
rs372352409	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10031792	TAAAAAATTCGGATT[C/G]CTAGGTCCCATTCCC	2177
rs372382609	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10047108	TTTTGCCAGCTGAAC[G/T]TTCAGGATATTAGCA	2177
rs372456357	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10047693	ATTTAACTTCTTTGA[A/G]CTTAAAAGTCAATTA	2177
rs372465674	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084442	CTGCAGGCATGTACC[A/G]CCATGCCCAGCTGAT	2177
rs372476346	snp	C/T	0.000437904	0.0147905	intron-variant	FANCD2	GRCh38.p7	3:10079301	GAAAGGCACTTGGAA[C/T]AAGAAATGTATTTCT	2177
rs372480518	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10037297	ACTGTATCAAAATAG[C/T]AAATAATAACTATTA	2177
rs372506747	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10048222	AGACTTGACTGGTGG[A/C]TCTAACTCTGTGTTC	2177
rs372534421	snp	C/T	0.000184522	0.00960349	missense	FANCD2	GRCh38.p7	3:10043848	TTGAAAACACTGCCT[C/T]AGTATCTGAACACAA	2177
rs372574627	snp	A/G	0.000280031	0.0118295	missense	FANCD2	GRCh38.p7	3:10078093	CAGGCTACAGAAGTT[A/G]TGCAACTTGGGCCCC	2177
rs372575998	in-del	-/A	0.0197687	0.0974348	intron-variant	FANCD2	GRCh38.p7	3:10078333	CAGCCGTATTGCCAG[-/A]CAATATTCATCTTGC	2177
rs372595278	snp	C/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096745	CCAGTACAAACCTCT[C/G]TCCACAGCTAGAGGA	2177
rs372597060	snp	C/G	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10030489	ACTAGGTTATTGGAA[C/G]TTAAGTCTGATTCTT	2177
rs372604284	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10073923	GCCAGATCATTCTGG[C/T]CCCTAAGCTCACAGT	2177
rs372617424	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10070755	AGAAAGAAGTAGACA[C/T]GGGAGACTTTTCATT	2177
rs372639953	in-del	-/T			intron-variant	FANCD2	GRCh38.p7	3:10041905	AGAGTCACAGGTCTG[-/T]TTTTTTTTTTTGAGA	2177
rs372696571	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088751	ATTGTTAATTCAGAT[C/T]ATAGAGGAATTAGAG	2177
rs372864245	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10057852	AATGAGGACCACCCA[A/G]CAAGATATTCTGTCA	2177
rs372885040	snp	C/G	0.00159617	0.0282053	upstream-variant-2KB, nc-transcript-variant	FANCD2, CIDECP	GRCh38.p7	3:10026041	AGGGAGGGCGCTGAC[C/G]TGTCAGATACTTGTT	2177
rs372887094	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10045248	ATCTCGGCTCACTGC[A/G]AGCTCCGCCTCCTGG	2177
rs372896393	snp	A/G	6.72766e-05	0.00579946	intron-variant	FANCD2	GRCh38.p7	3:10049332	TTAGAATGGCCATCC[A/G]TATTTTGTTTTACAC	2177
rs372903790	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10079221	TGCACTCCAGCCTGG[A/G]CATTAGAACAAGACT	2177
rs372905962	in-del	-/CT			intron-variant	FANCD2	GRCh38.p7	3:10048302	TCAAAACATGAGACA[-/CT]TTTTTTTGTTTTGTT	2177
rs372968936	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10045120	GGAAGCATAGACTCA[C/G]GTTGCCCTGAATACA	2177
rs372974292	snp	A/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084203	TTCACCATCTTGGCC[A/T]GGCTGGTCTTGAACT	2177
rs373001359	snp	A/G	1.6473e-05	0.00286988	intron-variant	FANCD2	GRCh38.p7	3:10064433	TGTTCCGGAAGGGTA[A/G]GTATTGTTTACCTGC	2177
rs373006120	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091701	GGAAAGGAAATTAAA[C/T]TAGGAACTCTTTGAA	2177
rs373010730	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10070110	GCGCCTCTGCCCGGC[C/T]GCGACCCCGTCTGGG	2177
rs373030388	snp	C/T	0.00358779	0.0422022	intron-variant	FANCD2	GRCh38.p7	3:10051146	AGCACTTTGGGAGGC[C/T]GAGGTGGGCGGATCA	2177
rs373107368	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025484	ACTGCAATGAAGTAT[A/G]TGAGGAAGTTGCCTC	2177
rs373112049	snp	C/T	1.65263e-05	0.00287452	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10098991	GGGACCCAGAAGAAA[C/T]AACGACACAATCTTA	2177
rs373195489	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10034011	CAAAGCTAAGTCTTT[C/T]ATGTGGGTTTAGACA	2177
rs373232961	snp	G/T	0.000414372	0.014388	intron-variant	FANCD2	GRCh38.p7	3:10043872	AACACAAGGTAATGT[G/T]CATGTACTATGCATT	2177
rs373260556	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092309	CAGAAACCAAGTGTC[C/T]TGGCTTCCAAAATGG	2177
rs373271103	snp	A/T	0.000347939	0.0131852	intron-variant	FANCD2	GRCh38.p7	3:10078029	AAAGAAAAAAAATTA[A/T]CATGAAATGACTAGG	2177
rs373289906	snp	A/T	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10039041	CTTCTCTCTAAATCC[A/T]CCCTGGATGTAGTCA	2177
rs373302152	snp	C/G			upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026357	CTTCAGCTGGGCTGC[C/G]CGGCCTTCCACTTCC	2177
rs373332685	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10054644	GCCCGCCACCACGCC[C/T]GGCTAATTTTTTGTA	2177
rs373337896	snp	G/T	3.29457e-05	0.00405854	missense	FANCD2	GRCh38.p7	3:10064420	TGGACTCCTGTGTTG[G/T]TCCGGAAGGGTAGGT	2177
rs373343140	snp	A/G	3.314e-05	0.00407049	intron-variant	FANCD2	GRCh38.p7	3:10039886	AAGTGAGGCTCAGCT[A/G]TGGGGGTTCTATCAC	2177
rs373461068	snp	A/T	0.000164715	0.0090736	synonymous-codon	FANCD2	GRCh38.p7	3:10065481	AAACTTGGAGGAGAT[A/T]GATGGTCTACTAGGT	2177
rs373593572	in-del	-/C			utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101377	TCCTTTTTTGTTCCT[-/C]TTTTTTTTTTTTTTT	2177
rs373593907	snp	A/G	0.000875616	0.0209055	intron-variant	FANCD2	GRCh38.p7	3:10062272	TTTTTAGAGAGTCTC[A/G]CTCTGTCACCCAACC	2177
rs373595588	snp	A/C	0.000280127	0.0118315	intron-variant	FANCD2	GRCh38.p7	3:10060259	TTTGCTGTGCCATTC[A/C]AGCATTTTCATCTTT	2177
rs373600764	snp	C/T	4.94629e-05	0.00497283	synonymous-codon	FANCD2	GRCh38.p7	3:10036317	ACCTTATTTGAGAAG[C/T]TGCCAGAATATTTTT	2177
rs373675448	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10047746	TGATGCTGAGAGTAA[A/T]CTCAGAATGATGAAG	2177
rs373685514	snp	A/G	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10075915	TTTTGTATTTTTAAT[A/G]GAGACGAGGTTTCAC	2177
rs373738236	snp	A/G	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10075209	TTTTTTTGAGATGGA[A/G]TCTCTCTCTGTCGCC	2177
rs373757862	snp	A/T	1.64727e-05	0.00286986	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088874	AAGGCCATAGAGGAG[A/T]TTGCTGGTGTTGGTG	2177
rs373774818	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10049111	GAAAGAGGAAAACTA[C/T]GCCAAGGAGCAAAAT	2177
rs373795013	snp	C/G	8.7033e-05	0.00659613	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095159	AATCTAAAATGAAAT[C/G]AGGACATTTCATAGA	2177
rs373802239	snp	A/G/T	0.000362527	0.0134592	intron-variant	FANCD2	GRCh38.p7	3:10035281	TGGAAGAGGTTTGTG[A/G/T]TGTATGCTCAAGTCT	2177
rs373821471	snp	G/T			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027434	ACTGAGACCACGAAG[G/T]TTCTGATTTACAAGA	2177
rs373835427	snp	C/T	0.000166853	0.00913229	synonymous-codon	FANCD2	GRCh38.p7	3:10039325	CTCATTGTCAGTCAA[C/T]TAAAATGGCTTGACA	2177
rs373838064	snp	C/T			upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10024994	CGAGGCTGCAGTGAT[C/T]GAGGCTGCAATCGCA	2177
rs373852822	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10079699	TGGTTTCAACAGCCT[A/C]CCAAACCAAGCCTGG	2177
rs373898927	snp	A/C/T	6.5895e-05	0.00573967	missense, synonymous-codon	FANCD2	GRCh38.p7	3:10047944	ATGTGTTCATCCATT[A/C/T]TGTCGCTGGCTCAGA	2177
rs373901619	in-del	-/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096870	GTCTTATTCCAGAAA[-/T]TACAAATTAATCTCT	2177
rs373904360	snp	A/G	3.30748e-05	0.00406649	intron-variant	FANCD2	GRCh38.p7	3:10034427	TAGAGAAGGAAAACT[A/G]TGGTAGGAAACTGGT	2177
rs373904701	snp	G/T	0.00034636	0.0131552	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10098976	GCTTATATAATTTTT[G/T]GGACCCAGAAGAAAC	2177
rs373906391	snp	C/T	1.64751e-05	0.00287007	intron-variant	FANCD2	GRCh38.p7	3:10078217	GTGTAGGCAGAAGCA[C/T]AGGACTTGGGCATAG	2177
rs373948218	in-del	-/GTT			intron-variant	FANCD2	GRCh38.p7	3:10029798	GTTGTTGTTGTTGTT[-/GTT]TGAGACGGAGTCTCA	2177
rs373979294	in-del	-/CATAG			intron-variant	FANCD2	GRCh38.p7	3:10047659	TTGAGCAGATAGGAA[-/CATAG]TGTTCTATTAGGCTT	2177
rs373986222	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10072178	AAGAAATGATAAATG[C/G]TTGAGGTGATGGATA	2177
rs374019283	snp	C/T	8.23689e-05	0.00641698	synonymous-codon	FANCD2	GRCh38.p7	3:10039759	GCTGATCAGTATTGC[C/T]CCAGAGAACCTGCAG	2177
rs374028735	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10064577	CCCCAGCACCCCTGC[A/T]CCCTTAGCTCCAAAA	2177
rs374031026	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10034445	GTAGGAAACTGGTGA[C/T]CAGCTCTTCTTTTTT	2177
rs374072890	snp	A/C/G	3.31018e-05	0.00406817	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096278	ATAAGAAATGTGAAG[A/C/G]CATGATGATAAACTC	2177
rs374084131	snp	A/G/T	0.000169252	0.00919781	intron-variant	FANCD2	GRCh38.p7	3:10065997	GAGCAGAGTTAATAG[A/G/T]ATGTTTCACTTATTG	2177
rs374096504	in-del	-/CC			utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101374	GGATCCTTTTTTGTT[-/CC]TCTTTTTTTTTTTTT	2177
rs374096957	snp	C/T	0.000230643	0.0107363	intron-variant	FANCD2	GRCh38.p7	3:10065509	GGTATGGGATGAAGT[C/T]ATCAGATCCTTTCTT	2177
rs374124262	snp	A/G/T	3.37105e-05	0.0041054	intron-variant	FANCD2	GRCh38.p7	3:10072821	AATTTCAAGTCTAAT[A/G/T]GTGGTGTGTAATTGG	2177
rs374169549	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10043755	TAGATGAGATAACAG[G/T]GCATGCTGAATAAGG	2177
rs374194873	snp	A/C	6.59294e-05	0.00574111	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093359	TGTTTCATATTTATT[A/C]TTCCTGTGGATCACT	2177
rs374213142	in-del	-/A			intron-variant	FANCD2	GRCh38.p7	3:10067990	TTTCATCATAAAAAA[-/A]CCCTCAGAAAACTGG	2177
rs374224525	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10049686	TCTCTATTCTGGGTG[C/T]TGTGAATGTAAAGTA	2177
rs374254573	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10047661	TGAGCAGATAGGAAT[A/G]TTCTATTAGGCTTGT	2177
rs374269022	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10044030	AAGATAATCTGAGGT[C/G]GCGACTGGCCAGATA	2177
rs374269740	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10032112	GGCCTCCCAAAGTGC[C/T]GGGATTACAGGCGTG	2177
rs374303202	snp	A/G	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10063479	GAGAGAAAACAGAGA[A/G]CCTTGCATGTAAAGC	2177
rs374304935	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10031663	TGGGATTAAACCTAT[C/T]TGAGCATTGTAGTCA	2177
rs374328858	snp	C/T	0.000153988	0.00877328	stop-gained	FANCD2	GRCh38.p7	3:10041684	GTCCTTTCAAGCCTC[C/T]GACTTGACCCAAACT	2177
rs374342941	in-del	-/G			intron-variant	FANCD2	GRCh38.p7	3:10048305	AACATGAGACACTTT[-/G]TTTTTGTTTTGTTTT	2177
rs374343764	snp	A/T	1.64814e-05	0.00287061	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096352	CACGAGACTCACCCA[A/T]CATGTGCCTCTGCTC	2177
rs374345567	snp	C/G	4.52694e-05	0.00475738	intron-variant	FANCD2	GRCh38.p7	3:10067349	ATACTGGTAGTACTA[C/G]TAGGCCAGTAGTGAG	2177
rs374444841	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10040909	TTAGCATCTGTCACC[G/T]TCTGTTGGGCGCAGT	2177
rs374445993	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10048282	AGATCCAGATCTAGT[C/T]CATTTCAAAACATGA	2177
rs374497481	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10077371	GACTAGCCTGGCCAA[C/T]GTGATGAAACCCATT	2177
rs374536709	snp	C/T	0.00279162	0.0372561	intron-variant	FANCD2	GRCh38.p7	3:10061421	CAGAGTGTGCAACTC[C/T]AGTTAAGAGTTCAGT	2177
rs374542781	snp	A/G	0.00953873	0.0683987	intron-variant	FANCD2	GRCh38.p7	3:10076356	GGATATTTAGGAAAC[A/G]CATCTTGGATCCACA	2177
rs374549151	snp	A/C			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094158	AATAAACCTTTTGGA[A/C]CCTTCCCAATTTGTT	2177
rs374597517	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092550	CCTCTATGATCTGAG[C/T]GCACATTCCCTCTTC	2177
rs374634490	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10047735	TGGAATCCCATTGAT[C/G]CTGAGAGTAATCTCA	2177
rs374714658	snp	C/G	3.38495e-05	0.00411383	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090247	CCCAGGTAGTTCTAA[C/G]CAGTGCATCATGGTG	2177
rs374761373	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10052073	GACTAAGCAGTAGAT[C/G]ATTAAAGCCCAGGAT	2177
rs374776972	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10077883	TAATTAAAAAAAAAA[A/C]TGTAGCTGGGCATGG	2177
rs374862529	snp	A/G	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10055573	ATCCCAGCACTTTGG[A/G]AGGCTGAGGCGGGCA	2177
rs374932184	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10033632	GGAGCAGATTATTCT[A/G]TCTTGCTAAGGTTAT	2177
rs374932802	snp	G/T	1.69977e-05	0.00291523	intron-variant	FANCD2	GRCh38.p7	3:10060428	GAGATTCTGACTTCT[G/T]TGGTTTAAGATCAGT	2177
rs374940277	snp	C/T	6.93421e-05	0.00588781	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090378	GCACAGCAGCAGACT[C/T]GCAGCAGGTGAGTAA	2177
rs374941138	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10063642	TATCAGAAGGAGACA[A/G]ACGGGTCAGAACATT	2177
rs374988769	snp	A/G	0.00159617	0.0282053	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093213	AAAGCTGTGCTTTGC[A/G]CAGCGGGAAAGAGGC	2177
rs375035465	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10055337	CCATCTTCCTCTCCC[C/T]ACCCCCTAATAATCA	2177
rs375085905	in-del	-/GTTTTTT	0.0138799	0.0821421	intron-variant	FANCD2	GRCh38.p7	3:10073936	GCCCCTAAGCTCACA[-/GTTTTTT]GTTTTTTGTTTTTTG	2177
rs375099172	snp	A/C/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10050572	AGCTTGCAGTGAGCC[A/C/G]AGATAACACCACTGC	2177
rs375142765	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10078947	GATTTCGTCTCAAAC[A/C]AAAAAAAAAGTCTAC	2177
rs375152499	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10051253	GGGCGTAGTGGTGGG[C/T]GCCTGTAGTCCCAGC	2177
rs375222243	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10053780	TGCCCTCAAAAAGCT[C/T]TGTCTGTTAGGGTAG	2177
rs375230570	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087920	CCAAAGTGCTGGGAT[C/T]ACAGACGTGAGCCAC	2177
rs375340538	in-del	-/G			intron-variant	FANCD2	GRCh38.p7	3:10047310	TGTAATTTTCTAGAT[-/G]GCAGAAACCACATGT	2177
rs375340940	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10048302	TCAAAACATGAGACA[C/T]TTTTTTTTGTTTTGT	2177
rs375344304	in-del	-/GGCGGCTGAGGTGGGACCATCACTTGAGTCCA	0.0611083	0.163768	intron-variant	FANCD2	GRCh38.p7	3:10077127	GATCCCAGCTACCTG[lengthTooLong]GGAGGTTGAGGCTGC	2177
rs375350046	in-del	-/AAG	0.0667012	0.170005	intron-variant	FANCD2	GRCh38.p7	3:10046726	TGTTCATTACTTAGT[-/AAG]TGTCAGAGACTATTG	2177
rs375375514	snp	C/G	0.000437904	0.0147905	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094231	GAGACTATTCTGCCT[C/G]AGGGGCCTTTCAGTG	2177
rs375385510	in-del	-/G			intron-variant	FANCD2	GRCh38.p7	3:10047584	AGGTGGAACATCCCT[-/G]GGGGGTAGTATGATT	2177
rs375386329	snp	C/T	5.01148e-05	0.00500549	intron-variant	FANCD2	GRCh38.p7	3:10043811	TAATATTTTTGTGAC[C/T]CTCTCCTGTTTTTTC	2177
rs375412395	snp	C/T	6.58957e-05	0.00573964	synonymous-codon	FANCD2	GRCh38.p7	3:10049400	TGCCTTAGTGACCCA[C/T]ATCTGCAGTGGGAAT	2177
rs375415579	snp	A/G	0.000153988	0.00877328	missense	FANCD2	GRCh38.p7	3:10067245	GAAACATCACCTGAG[A/G]TGAAGGGGAAGGTGC	2177
rs375426712	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10031363	AAAAAATTAGCCGGG[C/T]GTGGTGGTGTGCACC	2177
rs375435111	snp	C/G/T	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10044488	GCCTGGCCAATGTAG[C/G/T]GAAACCCCGTCTCTA	2177
rs375438721	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10053451	GTTAGTGGGTGCAGC[A/G]CACCAGCATGGCACA	2177
rs375506300	snp	A/G	1.64923e-05	0.00287156	missense	FANCD2	GRCh38.p7	3:10034514	TCTTTCAGACCCTGA[A/G]GAGACACCCTTCCTA	2177
rs375531367	snp	C/T	0.00041175	0.0143424	intron-variant	FANCD2	GRCh38.p7	3:10064703	ATTCCTGAGCTGCAA[C/T]ATCAGATTCTGGTTT	2177
rs375557064	snp	C/T	1.64743e-05	0.00287	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087126	TTGTTTTTCTTGTCT[C/T]CTTACAGCCAGAGCG	2177
rs375583022	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10055407	CCTCATATAAATGGA[A/G]TCATACGATATGTAT	2177
rs375588574	snp	G/T	0.0158469	0.0875917	intron-variant	FANCD2	GRCh38.p7	3:10040948	CCTTTAATCCCAGCA[G/T]GTTGGGCGGCTGAAG	2177
rs375595547	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10036935	CCACCTCCCAGGCTT[A/G]AGTGATCCTCACACC	2177
rs375610861	snp	A/G	0.000437904	0.0147905	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092123	TATCTTAGTGGGAAT[A/G]CAGTAAGGGAAGTAT	2177
rs375619463	snp	A/G	1.65636e-05	0.00287776	intron-variant	FANCD2	GRCh38.p7	3:10036358	AGTGGCGTTATTATG[A/G]AATGTTCAAAGTACC	2177
rs375632206	snp	A/G	0.000231321	0.0107521	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10098992	GGACCCAGAAGAAAC[A/G]ACGACACAATCTTAG	2177
rs375637341	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10040659	GAGAACAATATCCCT[A/C]GGTAATAAAGTTTCC	2177
rs375679113	snp	A/G	3.55492e-05	0.00421585	intron-variant	FANCD2	GRCh38.p7	3:10039395	TTGAATTTAAAGAGT[A/G]TGTTTCTCATATCTT	2177
rs375699343	snp	A/G	1.65012e-05	0.00287234	intron-variant	FANCD2	GRCh38.p7	3:10041593	TGTTCAAACCATTAT[A/G]CAACTTTTTTCTTTT	2177
rs375700178	in-del	-/T			intron-variant	FANCD2	GRCh38.p7	3:10037140	CTACCTGTTTTTTTT[-/T]AATTACTATGTTAAG	2177
rs375736661	in-del	-/CGGCTGAGGTGGGACCATCACTTGAGTCCAGG			intron-variant	FANCD2	GRCh38.p7	3:10077129	TCCCAGCTACCTGGG[lengthTooLong]AGGTTGAGGCTGCAG	2177
rs375758434	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10048341	GTGGTTTTGCTCTTC[A/T]TGCCCAGGCTGGAGT	2177
rs375792717	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10048241	AACTCTGTGTTCTGA[A/G]CTCTAAAATTCTCTG	2177
rs375827113	snp	C/G/T	8.25817e-05	0.00642533	FANCD2	3	allele_origin=T(germline)/C(germline)	3:10072931	CTTTAGATATAACAC[C/G/T]TCATACTGTTACTGC	2177
rs375829116	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10052118	AAGAGGATAAAGAAA[A/G]CTTTATGTTTCCTGA	2177
rs375843081	snp	C/T	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10070365	GCCAGCCGCCCCGTC[C/T]GGGAGGGAGGTCAGG	2177
rs375877292	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10070787	TGTTCTGTACTAAGA[A/T]AAATTCTTCTGCCTT	2177
rs375879400	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10052855	ACCAGTTAGAATGGC[A/G]ATCATTAAAAAGTCA	2177
rs375929975	snp	C/T	0.000181185	0.00951628	synonymous-codon, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10081405	GAAAGTTCAGGAGTA[C/T]CACATAATGTCTTCC	2177
rs375948560	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084227	TTGAACTCCTGACCC[C/T]GTGATCTACCCACCT	2177
rs375951862	snp	A/G	0.00014834	0.00861092	missense	FANCD2	GRCh38.p7	3:10063828	GTTCATTCCTGCAGT[A/G]AGCAGTCTCCTCAGG	2177
rs375996302	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10042401	ACAACTAAAAGATTC[C/T]AATTTGGGGAAAAAT	2177
rs376000069	snp	G/T	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10050937	CTAAAAATACAAAAA[G/T]TACCTGGGCATTGTG	2177
rs376013316	in-del	-/AT	0.346154	0.230769	intron-variant	FANCD2	GRCh38.p7	3:10054337	CTTTGAACAACCAGC[-/AT]ATATATATATATACG	2177
rs376036728	in-del	-/CTT	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10079759	CTAGAACGTCCAGAA[-/CTT]CAGATGTGTATACAG	2177
rs376073958	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10054410	ACGTATATGTATATA[C/T]GTATATACATATATA	2177
rs376076858	snp	C/T	0.030665	0.119967	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091502	AGAAAAAACATATAC[C/T]GGCTGTAGCTTCTCT	2177
rs376086993	snp	A/G	1.648e-05	0.0028705	intron-variant	FANCD2	GRCh38.p7	3:10063761	AAGATTGGCAGCCCA[A/G]GGTTTAAACCATTCT	2177
rs376114632	snp	A/C	1.65274e-05	0.00287462	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093238	AGAGGCTGGAGTGCT[A/C]AAAGGAGCAGATCTC	2177
rs376148489	snp	A/G	0.00318978	0.0398085	intron-variant	FANCD2	GRCh38.p7	3:10033989	GGCATGAGCCACCGC[A/G]CCCAGCCAAAGCTAA	2177
rs376161031	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10057109	GATCCACCCACCTCT[A/G]CCTCCCAAAGTGCTG	2177
rs376274187	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10042820	TCTATATAAGCTGCT[A/T]TAAGTTACATTTACT	2177
rs376281171	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10039958	TAAAAAGAGGATGAT[A/G]CCCCCCTTCATGAGT	2177
rs376284620	snp	G/T	0.0111196	0.0737302	intron-variant	FANCD2	GRCh38.p7	3:10070119	CCCGGCCGCGACCCC[G/T]TCTGGGAGGTGAGGA	2177
rs376289007	snp	C/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086538	ACTTTGTCACCCAGG[C/G]TGGAGTGATCCCAGC	2177
rs376303652	snp	A/G	0.000153988	0.00877328	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101164	TAACCTAAAATGCTT[A/G]TTTATTTATTCTTTG	2177
rs376349741	snp	C/G/T	0.000346169	0.0131518	missense, synonymous-codon	FANCD2	GRCh38.p7	3:10046588	ACAATAGGTGTTTGA[C/G/T]CTGGTGATGCTTTTC	2177
rs376351939	snp	C/G	0.000153988	0.00877328	intron-variant	FANCD2	GRCh38.p7	3:10043014	CTACCCACTATGAAT[C/G]AGCAGAAAACCATAG	2177
rs376361706	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10069610	GCGATTGCAGGCGCG[C/T]GCCGCCACGCCTGAC	2177
rs376378807	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100993	GGAATCGCTTGAACC[C/T]GGGAGGCAGAGGTTG	2177
rs376394589	in-del	-/T			intron-variant	FANCD2	GRCh38.p7	3:10037011	AGCTAATTTTCGTGG[-/T]TTTTTTTTTTTTTGG	2177
rs376427490	snp	A/G	3.29603e-05	0.00405944	intron-variant	FANCD2	GRCh38.p7	3:10078249	GGATTTGGGAACAAA[A/G]GAGGTATTATGATGA	2177
rs376442380	snp	A/G/T	0.00011531	0.00759228	intron-variant, missense	FANCD2, FANCD2OS	GRCh38.p7	3:10098852	GAGTCTGGCACTGAT[A/G/T]GTTGCATTTTGTTAA	2177
rs376442786	snp	C/T	8.24042e-05	0.00641836	intron-variant	FANCD2	GRCh38.p7	3:10078030	AAGAAAAAAAATTAT[C/T]ATGAAATGACTAGGA	2177
rs376453915	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10047756	AGTAATCTCAGAATG[A/G]TGAAGGATTATTTTT	2177
rs376471978	snp	A/G	0.000168353	0.00917323	intron-variant	FANCD2	GRCh38.p7	3:10043784	GGTGTAACGTGTTTC[A/G]CTGATGTGTCATAAT	2177
rs376473059	snp	C/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085055	CAAAGATAGAAATGT[C/G]AAGACTTGACTCATT	2177
rs376488313	snp	A/G	8.24029e-05	0.00641831	intron-variant	FANCD2	GRCh38.p7	3:10041612	CTTTTTTCTTTTTCT[A/G]CCATTCACAGTGACC	2177
rs376489415	in-del	-/CT			utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101375	GATCCTTTTTTGTTC[-/CT]CTTTTTTTTTTTTTT	2177
rs376514610	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10038781	AGATGGGGTTTCACC[A/G]TGTTGGCCAGGCTGG	2177
rs376543284	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10059492	TTTTTATAATGTATC[A/G]CTAATCCTTAAAACA	2177
rs376548559	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10048328	TTTGTTTTGAGACGT[A/G]GTTTTGCTCTTCATG	2177
rs376637471	snp	A/G	0.00159617	0.0282053	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096705	CCATTGATATAAACA[A/G]TGCCTCAGACATAAA	2177
rs376653492	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10047724	TTATCCAAACGTGGA[A/C]TCCCATTGATGCTGA	2177
rs376654972	snp	C/T	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10057652	ACAGGCATGAGCTAC[C/T]GCTCCCGGCCTCCAT	2177
rs376680433	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10034448	GGAAACTGGTGACCA[C/G]CTCTTCTTTTTTCTG	2177
rs376698548	snp	A/G	1.88276e-05	0.00306813	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098682	ACCCTAAATGTGATC[A/G]TTATAACCCACCATT	2177
rs376708399	snp	A/G	3.32441e-05	0.00407688	missense	FANCD2	GRCh38.p7	3:10049479	TTAAACCCATCTGCT[A/G]TGATGATGAATGCTG	2177
rs376733483	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10047742	CCATTGATGCTGAGA[A/G]TAATCTCAGAATGAT	2177
rs376755596	in-del	-/TTTA	0.0236746	0.106192	intron-variant	FANCD2	GRCh38.p7	3:10078348	CAATATTCATCTTGC[-/TTTA]TTTATTTATTTATTT	2177
rs376759262	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10063725	AAAAACAGTCTTGAA[A/T]GGGGCGAGTGGAGTT	2177
rs376759279	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10075823	GCAAGCTCCGCCTCC[C/T]GGGTTCACACCATTA	2177
rs376778292	in-del	-/TATTGATG			intron-variant	FANCD2	GRCh38.p7	3:10045553	TTTCCTGTATTGATG[-/TATTGATG]GGCATTTATAGTCTT	2177
rs376783877	in-del	-/T			intron-variant	FANCD2	GRCh38.p7	3:10037140	TACCTGTTTTTTTTT[-/T]AATTACTATGTTAAG	2177
rs376809847	snp	A/G	1.64838e-05	0.00287083	intron-variant	FANCD2	GRCh38.p7	3:10035283	GAAGAGGTTTGTGGT[A/G]TATGCTCAAGTCTAA	2177
rs376820936	snp	C/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097329	CTCTTCCTAATAAGC[C/G]TGGGAGCGCTATAGG	2177
rs376828609	snp	A/G	1.6473e-05	0.00286988	synonymous-codon	FANCD2	GRCh38.p7	3:10065490	GGAGATTGATGGTCT[A/G]CTAGGTATGGGATGA	2177
rs376836572	snp	A/G	1.64811e-05	0.00287059	missense, downstream-variant-500B	FANCD2, FANCD2OS	GRCh38.p7	3:10081152	AACAGAGATCTGCCC[A/G]AGAAATTGTTCATTG	2177
rs376843077	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10041927	TTTTTGAGACGGAGT[A/G]TCACTCTGTCACCCA	2177
rs376913349	snp	C/G	3.29853e-05	0.00406098	intron-variant	FANCD2	GRCh38.p7	3:10074686	GAAGTAAGTGACAGG[C/G]TAGGATCTCAGAATT	2177
rs376931896	snp	A/G	0.000329984	0.0128407	intron-variant	FANCD2	GRCh38.p7	3:10036256	GTGTATTTTGAGATC[A/G]TCTCCTAACTCCCTA	2177
rs376954742	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10079786	ATACAGTGTACAAAC[A/G]TGCACCTAGCATCCG	2177
rs376998379	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10055547	GCCGGGCACGGTGAC[G/T]CACGCCTGTAATCCC	2177
rs377014960	in-del	-/G			intron-variant	FANCD2	GRCh38.p7	3:10034346	AAAAAAAAAAAAAAA[-/G]ATTTGTCTCTGAAAT	2177
rs377014993	snp	C/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097266	CTTATCAGGAGACAG[C/G]GTTTTGAGATCAACA	2177
rs377046496	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10030501	GAAGTTAAGTCTGAT[A/T]CTTGGTCAATTCAAC	2177
rs377083479	snp	A/G/T	0.000181875	0.00953467	missense	FANCD2	GRCh38.p7	3:10065930	TGTCTGCTAAAGAGC[A/G/T]TTCATTCATGTGTTC	2177
rs377144926	snp	A/C/T	6.58928e-05	0.00573957	intron-variant	FANCD2	GRCh38.p7	3:10064685	TTCCCTGTAGCCTTG[A/C/T]GTATTCCTGAGCTGC	2177
rs377174615	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10055087	GCTTTTGCATTTAGC[A/G]GTTTATTTTGGAGAT	2177
rs377211339	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10033654	TAAGGTTATGGCAGG[G/T]CTTTTTTAGAACACT	2177
rs377211883	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10030439	ATTCTCATAGCTTAG[C/T]TTCTACTGACTTGTG	2177
rs377224413	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10078918	TGCACCAGTGCACTC[A/C]AGTCTGGGTGACAGA	2177
rs377227474	snp	A/C	1.70104e-05	0.00291632	missense	FANCD2	GRCh38.p7	3:10043857	CTGCCTCAGTATCTG[A/C]ACACAAGGTAATGTT	2177
rs377227974	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10058305	ATAATTCTGTTTTTC[A/G]TCGCTGGCACCACGA	2177
rs377385269	in-del	-/GTTGTCG			intron-variant	FANCD2	GRCh38.p7	3:10048313	ACACTTTTTTTTGTT[-/GTTGTCG]TTGTTTTGAGACGTG	2177
rs377390526	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10078839	GGGCATGGTGGTGCA[C/G]CTATAGTTCCAGCTA	2177
rs377404568	snp	A/G	0.000153988	0.00877328	intron-variant	FANCD2	GRCh38.p7	3:10078220	TAGGCAGAAGCATAG[A/G]ACTTGGGCATAGTGG	2177
rs377490218	snp	C/T	0.000165382	0.00909196	missense	FANCD2	GRCh38.p7	3:10060394	TGGCTGGCATCATGG[C/T]GGCAGACAGGTACAC	2177
rs377539937	snp	A/G	2.40382e-05	0.00346677	intron-variant	FANCD2	GRCh38.p7	3:10067181	TCTGAACATTTGGAA[A/G]TATGAGAATGTAATT	2177
rs377575923	in-del	-/T			intron-variant	FANCD2	GRCh38.p7	3:10047767	AATGATGAAGGATTA[-/T]TTTTGTGTAAAACAA	2177
rs377607295	multinucleotide-polymorphism	CA/GG			intron-variant	FANCD2	GRCh38.p7	3:10032140	GTGAGCCACTGTGCT[CA/GG]GTCGGAAATATGCAT	2177
rs377609776	snp	A/G	0.031825	0.122064	intron-variant	FANCD2	GRCh38.p7	3:10051368	CCTGGGCGACAGAGC[A/G]AGACTCCGTCTCAAA	2177
rs377610730	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10070319	GGCAGCCACCCCGTC[A/C]GGGAGGGAGGTGGGG	2177
rs377626796	snp	C/T	6.58903e-05	0.00573941	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094291	CTCTCTTCTTCAGTA[C/T]GGGCGTCTCTTTGTG	2177
rs377658972	snp	C/T	0.00119737	0.0244387	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10089530	GCTGGAGTGCAGTGG[C/T]GTAATCTCAGCTCAC	2177
rs377716703	snp	A/G	0.000153988	0.00877328	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088587	AAATAGCTTTTTTCT[A/G]TTTTGCTACTGTTGT	2177
rs377718759	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10054584	CGCCTCCCAGGTTCC[C/T]GCCATTCTCCTGCTT	2177
rs377721420	snp	C/T	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10071838	AGTCTCGGCTTACTG[C/T]GACCTCTGCCTCCTG	2177
rs377723227	snp	C/T	1.64743e-05	0.00287	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088969	AGGGAGTTCTTTCCT[C/T]CAGTTTTTCCCTTAA	2177
rs377737159	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10031669	TAAACCTATCTGAGC[A/G]TTGTAGTCAAAGATA	2177
rs386658333	multinucleotide-polymorphism	ATT/GTC			intron-variant	FANCD2	GRCh38.p7	3:10031497	ACAGAGCAAGACTCC[ATT/GTC]TCAAAAAAAAAAAAA	2177
rs386658334	multinucleotide-polymorphism	CA/TG			intron-variant	FANCD2	GRCh38.p7	3:10042191	TTGAGCCACCGTGCC[CA/TG]GCCCACAGGTCTGTT	2177
rs386658335	multinucleotide-polymorphism	CTC/GTG			intron-variant	FANCD2	GRCh38.p7	3:10047066	TGTAAATTATTCAAA[CTC/GTG]GAATTTTATAAGCTA	2177
rs386658336	multinucleotide-polymorphism	CGC/TGT			intron-variant	FANCD2	GRCh38.p7	3:10047192	CTAATGAGAATACCT[CGC/TGT]TGGGTCTTAAATTTT	2177
rs386658337	multinucleotide-polymorphism	CATAG/TGTTC			intron-variant	FANCD2	GRCh38.p7	3:10047660	TTGAGCAGATAGGAA[CATAG/TGTTC]TATTAGGCTTGTAAT	2177
rs386658338	multinucleotide-polymorphism	AG/TC			intron-variant	FANCD2	GRCh38.p7	3:10055912	GAGATGGAGTCTCAC[AG/TC]TGTCGCCCAGGCTTG	2177
rs386658339	multinucleotide-polymorphism	ATA/TTG			intron-variant	FANCD2	GRCh38.p7	3:10068306	AGATACAAAATCATC[ATA/TTG]TAAAAATGAGTAGCA	2177
rs386658340	multinucleotide-polymorphism	CC/TG			intron-variant	FANCD2	GRCh38.p7	3:10071884	CCTGCCTCAGCCTCC[CC/TG]AGTAGCCGGGACTAG	2177
rs386658341	multinucleotide-polymorphism	AGT/CAC			intron-variant	FANCD2	GRCh38.p7	3:10075253	AGTGGCGCGGATCTC[AGT/CAC]TCACTGCAAGCTCTG	2177
rs386658342	multinucleotide-polymorphism	CA/TG			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098332	CTGAAACCACCTCAC[CA/TG]TACTGTCCTTTAGCC	2177
rs397897245	in-del	-/T	0.416522	0.186468	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097990	GAGCATTTATAAGGT[-/T]TTTTTTAGTTGTCTG	2177
rs397897610	in-del	-/TT			intron-variant	FANCD2	GRCh38.p7	3:10035167	AGATTTCTTTTTTTT[-/TT]ACAGTATGGGTGCAT	2177
rs397897611	in-del	-/A			intron-variant	FANCD2	GRCh38.p7	3:10040002	TGACTTAAAAAAAAA[-/A]GGTATATATTTGAAT	2177
rs397897612	in-del	-/A			intron-variant	FANCD2	GRCh38.p7	3:10062136	ATAATTTAAAAAAAA[-/A]TTCTTTGTTTTTAGA	2177
rs397948524	in-del	-/TTTTTTTTTTT			intron-variant	FANCD2	GRCh38.p7	3:10045101	TGTTTTTTTTTTTTT[-/TTTTTTTTTTT]CCTGGAAGCATAGAC	2177
rs397950663	in-del	-/TT			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095899	TTTTTTTTTTTTTTT[-/TT]GAGACGGAGTCTCGC	2177
rs397969910	in-del	-/TT			intron-variant	FANCD2	GRCh38.p7	3:10076296	GTCTTTTTTTTTTTT[-/TT]CCCAAACCCTGTGTG	2177
rs397988658	in-del	-/A	0	0	intron-variant	FANCD2	GRCh38.p7	3:10030112	CCAAACTCCATCTCA[-/A]AAAAAAAAAAAAAAA	2177
rs527252535	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10058176	GACCTGTCTTCCGCA[C/G]GAAGAGACCGTGGAG	2177
rs527312227	in-del	-/AAAA			intron-variant	FANCD2	GRCh38.p7	3:10067809	ATCTCAAAAACAAAC[-/AAAA]GAAAGATTATTCATC	2177
rs527351820	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10030764	AATTAGCTGGGCGTG[G/T]TGTCACGTGTCTGTA	2177
rs527369276	snp	C/G	3.29468e-05	0.00405861	missense	FANCD2	GRCh38.p7	3:10064411	CCTTCGTAGTGGACT[C/G]CTGTGTTGTTCCGGA	2177
rs527376977	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10055177	AAAATATACATAATA[C/T]AAAATAGACCGTTTA	2177
rs527411764	snp	A/T	0.00119737	0.0244387	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100884	AGACCAGCCTTGCCA[A/T]TGTGGAGAAACCCCG	2177
rs527444078	snp	C/T	0.0150606	0.0854603	intron-variant	FANCD2	GRCh38.p7	3:10069618	AGGCGCGCGCCGCCA[C/T]GCCTGACTGGTTTTC	2177
rs527501433	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10036039	GATATCAACTTTAGC[A/G]AAGTGTTTATTCCAG	2177
rs527507850	snp	C/T	1.64817e-05	0.00287064	intron-variant	FANCD2	GRCh38.p7	3:10063786	CATTCTTCCTCTTTG[C/T]TCCAGGTGACCTCCT	2177
rs527520419	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10069887	CCCGGCCGCCACCCC[A/G]TCTGGGAAGTGAGGA	2177
rs527572980	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10042020	TCCCTGACTCAGCCT[A/C]CCAAGTAGCTGGGGT	2177
rs527586831	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10075289	CCCGGGTTCACGCCA[C/T]TCTGCTGCCTCAGCC	2177
rs527701339	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10031334	TGGTGAAACCCCGTC[A/T]CTACTAAAAATACAA	2177
rs527710953	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10052856	CCAGTTAGAATGGCA[A/G]TCATTAAAAAGTCAG	2177
rs527711543	snp	A/G	1.64727e-05	0.00286986	synonymous-codon	FANCD2	GRCh38.p7	3:10065439	TTTCCGGTTACTGAG[A/G]CTTTGTGTGGAGAGA	2177
rs527769128	snp	C/T	8.28315e-05	0.00643497	synonymous-codon	FANCD2	GRCh38.p7	3:10043508	AAATCAAGAAAGCAG[C/T]GGTCAGAGCTGTATT	2177
rs527786976	snp	A/G	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10077063	GTGAGACCTGTCTCT[A/G]CAAAAAGTTAAAAAA	2177
rs527788333	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10070571	CGCCTCTGCCCGGCC[G/T]CCCCTACTGGGAAGT	2177
rs527799297	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10065715	TATTTGTTGATTGCT[A/G]TATGATATGCAAATA	2177
rs527809853	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10037564	TTAGTGCTTGCTTTG[A/G]CAGCACGTATACTAA	2177
rs527814804	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10031269	AGCACTTTGGGTGGC[C/T]AAGGCGGGCAGATCA	2177
rs527862925	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082047	TTCTGAGCTATAGGC[A/G]TTTATATCCAACTGC	2177
rs527926669	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10076485	ACATGCTTGACTTTA[C/T]TATATGACAGAGCAT	2177
rs527934206	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094939	AATGTTGCAGATGGG[A/G]AAACTGAGACATGGT	2177
rs527942969	snp	A/G	0.00119737	0.0244387	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087804	CAGGTGCGCACCACC[A/G]TGCCCAGCCAATTTT	2177
rs527954157	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10053112	TATTCACAATAGCAA[A/G]GACTTGGAACCAACC	2177
rs527995189	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088350	TTAGTAAATCTAAAC[C/T]AATAATCCTTTTGAT	2177
rs528028589	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10079199	CAGTGAACCAAGATC[A/G]TGCTACTGCACTCCA	2177
rs528064204	snp	G/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10067617	AGCCTGGCCAACATG[G/T]TGAAACCCTGTTTGT	2177
rs528089305	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027778	GGCGTGGTGGCGGGC[A/G]CCTGTAGTCCCAGCT	2177
rs528102726	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10033983	ATTACAGGCATGAGC[C/T]ACCGCGCCCAGCCAA	2177
rs528131902	snp	A/G	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10051958	ATGATATGGCAAGGA[A/G]TAGGGTAAAGACATA	2177
rs528167852	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10040020	TATATATTTGAATAG[A/G]TCCACATACTTTCTT	2177
rs528271200	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10045320	ACTACAGGCACCTGC[C/T]ACCACGCCCGGCTAA	2177
rs528315581	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10078721	GTAATGCCAGCACTT[C/T]GGGAGGCCAAGGAGG	2177
rs528343291	snp	G/T	0.00199481	0.0315187	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098042	TTTATAATACTACTT[G/T]GGAGTTACAACATTT	2177
rs528350503	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10050060	ACATAGGACAGGCCC[A/G]TGTTGCAAAGAGTCT	2177
rs528361161	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10037074	AGTCTCAAAACTTCC[A/G]GGCTCAAGTGGTCCA	2177
rs528402721	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091656	CAGTAGCCAAGGAAA[A/G]GAGAGCCCATTCCTC	2177
rs528447846	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086959	TTTCCATACAAAGGT[A/G]TGGTTTTCTACCAAG	2177
rs528451743	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10046249	TAGTAGAGACGGGGT[C/T]TCACCGTGTTAGTCA	2177
rs528477461	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10046355	ACTGTGCCTGGCCTG[C/T]TCTGTATTCTTAAGG	2177
rs528495689	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10041177	TGTACTCAAGCCTGG[G/T]CATCAGAGTAAGACC	2177
rs528580635	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086331	CTGAGGGGTAGGCAG[C/T]GGACAAGGGAGGTGA	2177
rs528698983	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10056889	AGATGGGGTCTCACT[C/T]TGTCACACACATTGG	2177
rs528716922	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10036002	AAATGAAGACATATT[C/T]GTGTGGATATCCTTG	2177
rs528734287	snp	A/C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10033356	CAGTGAGTCAAGATC[A/C/G]CACCACTGCACTCCA	2177
rs528736110	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10028589	CTCAGAATTTATCTT[C/G]TAGAGGGTAACTTCT	2177
rs528772355	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10062325	GGCTCACTGCAACCT[C/T]CACCTCTCAGGTTCA	2177
rs528772652	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10054645	CCCGCCACCACGCCC[A/G]GCTAATTTTTTGTAT	2177
rs528799808	snp	C/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084785	ACGTCAGATTGTGCT[C/G]GGCCTCAAAGGTCAG	2177
rs528812652	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098641	CTTCCTTTGTATTGC[C/G]TGTAAACTCAACCTT	2177
rs528854184	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090117	ATTGTTTGACAGGCA[A/G]TCTTCTTGGGCTTAT	2177
rs528856146	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082648	CTGCCAGGACCCCCA[A/C]TCTTCTTGATCCCCA	2177
rs528861649	snp	C/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10048590	GATTATAGGCGTGAG[C/T]CATTGGGCCTGGCCG	2177
rs528951364	snp	A/G	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10031427	GAATGGCATGAACCC[A/G]GGAGGCGGAGCTTGC	2177
rs528953711	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095919	CGGAGTCTCGCTTTG[C/T]AGCCCAGGCCGGAGT	2177
rs528988269	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10042074	GGCTAATTTTTGTAT[A/T]TTTAGTAGAGACGGG	2177
rs529087095	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025876	AGGGAGGTACTGTTA[C/T]TATCCCCATTTCACA	2177
rs529161683	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10065031	GATTCCTTGTTTTTT[A/C]TTGGATCCTTGGCTT	2177
rs529220545	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10062873	TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT	2177
rs529234039	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10036155	GGAGTGGTGCAATCT[C/T]GGCTCACTGCAATCT	2177
rs529243472	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025109	CAGGCACACACCACT[A/G]CACCTGGCTAATGTT	2177
rs529272391	in-del	-/AT	4.47507e-05	0.00473005	intron-variant	FANCD2	GRCh38.p7	3:10062136	ATAATTTAAAAAAAA[-/AT]TCTTTGTTTTTAGAA	2177
rs529308850	in-del	-/TTTTGTTTTTG	0.00358779	0.0422022	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090809	TTCTCCTAAGCTGTT[-/TTTTGTTTTTG]TTTTGTTTTGAGTTT	2177
rs529341771	snp	G/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10032281	TAGGCACTTATTTGT[G/T]TGAATTTATTTTTTT	2177
rs529418229	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10066718	TAGGGTCACAAGCCT[A/C]ATCTCCTTTGTTTTT	2177
rs529420518	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10060601	TGGAATGTGATCCTA[A/G]CCATTACAGTCTGTG	2177
rs529467403	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025737	TAAACCCACCGAGGG[C/T]TGGCGACTAACCTAA	2177
rs529515657	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10037878	TAAAAAAGAAGATAC[A/G]CACATACACATATGT	2177
rs529538557	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10072664	GTTTTATGATAATTG[A/G]TCATACTTAATATGA	2177
rs529551499	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10077224	AGCAACAGAGCGAGA[A/C]CCTGTCTCAAATATA	2177
rs529581935	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10077911	TGGTTGTGTGTGCCT[A/G]TAGTCCCCGCTACTC	2177
rs529586110	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10038560	TGACTTTCTATGTTC[A/C]CTTAGCAATATATGC	2177
rs529605892	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10044289	CTCATGTAGACCTGA[C/T]TAGAGTAAATCAATC	2177
rs529700269	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10053102	ATTGCGGCACTATTC[A/C]CAATAGCAAAGACTT	2177
rs529701922	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10029433	TTGAGCTCAGGAGGT[C/T]GAGGGTGCAATGAGT	2177
rs529754470	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096703	TGCCATTGATATAAA[C/T]AATGCCTCAGACATA	2177
rs529823667	snp	A/C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10069508	CGTCTCCCTCTGATG[A/C/T]CGAGCCAAAGCTGGA	2177
rs529893298	snp	A/G/T	1.64792e-05	0.00287042	missense	FANCD2	GRCh38.p7	3:10047917	TCTTCCCCACTCAAG[A/G/T]TTCTTAAGGATATGT	2177
rs529901192	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086235	CTACTGTCTCCCAGC[A/T]GATTTGGGTAATTAG	2177
rs529954046	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10046255	AGACGGGGTTTCACC[A/G]TGTTAGTCAGGATGG	2177
rs529959031	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10074714	ATTTAATCTTCTTTC[A/G]GAAAGTTCCTCAGGT	2177
rs529960759	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10069148	AAAAATGGACAAATG[A/G]GATCACATTAAGTTA	2177
rs530021452	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10079630	GCGCCCAGCCTACGA[A/C]ATGTATTTCTAAATG	2177
rs530022240	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10070137	TGGGAGGTGAGGAGC[A/G]TCTCTGCCCGGCTGC	2177
rs530055623	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10036761	CACAATATACTGGTA[A/G]TGGTAGTTGTCTCCA	2177
rs530083489	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10070382	GGAGGGAGGTCAGGG[A/G]GTCAGCCCCCCGCCC	2177
rs530106165	in-del	-/TTTTTTT	0.0209421	0.100162	intron-variant	FANCD2	GRCh38.p7	3:10036684	TATTTCAAAACAGAA[-/TTTTTTT]TTTTTTTTTAAGTAT	2177
rs530125285	snp	A/G	0.000131781	0.00811621	missense	FANCD2	GRCh38.p7	3:10042571	TAGGTTCGCCAGTTG[A/G]TGATGGATAAGTTGT	2177
rs530136960	snp	G/T	0.00557542	0.0525036	utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101417	TAAAGACGGGGACTC[G/T]CTGTGTTTCCCAGGC	2177
rs530160447	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081873	CTTTAGAGAGATAAC[A/G]GAAGGAAGTGGAAGG	2177
rs530174859	snp	C/T	0.0107246	0.0724382	intron-variant	FANCD2	GRCh38.p7	3:10080693	AGAGGATCACTTGAG[C/T]CCAGGAATTCAAGGC	2177
rs530200715	snp	C/T	1.64746e-05	0.00287002	synonymous-codon	FANCD2	GRCh38.p7	3:10046639	TCAGACAAAGAAGTA[C/T]ATTGACAGGGTGCTA	2177
rs530202330	snp	C/T	3.30251e-05	0.00406343	intron-variant	FANCD2	GRCh38.p7	3:10052379	TGTTGGCATCATTTT[C/T]TCCACAGGGCATTTT	2177
rs530257215	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10054040	CCATGGTGAAACCCC[A/G]TCTCTACAAAAACAT	2177
rs530258596	snp	C/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10079345	AGTCTCGCTGTGTCT[C/G]CCAGGCTGGAGTGCA	2177
rs530301423	snp	A/G	0.00199481	0.0315187	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100792	TATGCAAATTGGGCC[A/G]GGCGCAATGGCTCAC	2177
rs530308737	snp	A/G	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10058083	TCTTGGGATTCTCCA[A/G]ATACTCCATCAGTGT	2177
rs530311131	in-del	-/A	0.0418186	0.138422	intron-variant	FANCD2	GRCh38.p7	3:10054635	CTACAGGCGCCCGCC[-/A]ACCACGCCCGGCTAA	2177
rs530311832	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087783	CCTTTCAAGTAGCTG[A/G]GATTACAGGTGCGCA	2177
rs530364306	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10050413	GCAAATCACGAGGTC[A/T]GGAGATCAAGACCAT	2177
rs530379900	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10077758	GCTGGGCCCAGGTGT[A/G]GTGGTTCATACCTGT	2177
rs530389748	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093749	TTAGCCCTAGATTTG[A/G]TGGGAAGTCCAGTCA	2177
rs530398424	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10051799	GACAAACCATGAAAG[A/G]TAGTATAGCTATTAT	2177
rs530409738	snp	C/T	9.28893e-05	0.0068144	intron-variant	FANCD2	GRCh38.p7	3:10073029	TCTAAATAAGCTTCA[C/T]TGAATTAACCTAAAA	2177
rs530411786	snp	C/T			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027253	TGTGAGGTAAGGGCC[C/T]CTAGGTATACCCTGT	2177
rs530443502	in-del	-/T	0.372679	0.21783	intron-variant	FANCD2	GRCh38.p7	3:10041906	GAGTCACAGGTCTGT[-/T]TTTTTTTTTTGAGAC	2177
rs530448315	snp	A/G	1.64852e-05	0.00287094	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094394	AGAGAACAAAGATAT[A/G]CACTGAAGAGTTGCT	2177
rs530469695	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10073436	CCCAGCTTTATTCTC[A/G]GCATTTTACAAAGAA	2177
rs530517432	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10044921	CTTAACATTTTTTCT[C/G]CTGTCATAAATATTT	2177
rs530543468	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10032556	AAGTGATCCTCCTGC[C/G]TTGGCCTCCTAATTT	2177
rs530555525	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10039206	TGGCTAAAATATTTT[G/T]TGCAGTATTAATGCT	2177
rs530577368	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10048406	CCTCCTGGGTTCAAG[C/T]GATTCTCCTGTCTCA	2177
rs530583767	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10074908	ATGATGTAATCCTTA[C/T]ATTTAGGTTACTACT	2177
rs530588579	snp	C/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10054778	CTGAGCCACCGCACC[C/T]GGCCACAACCATCAT	2177
rs530643220	snp	G/T			utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101592	GGTTTTACCATGTCG[G/T]CCAGATGGTCTCAAT	2177
rs530653097	snp	A/G	0.00199481	0.0315187	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084718	ATTTGTTGAAAGGAA[A/G]AATGACTATCACTGG	2177
rs530863190	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097375	TCACCTCTGCAGTCT[C/T]GACCATAAGAGACAG	2177
rs530863250	snp	C/T	8.40725e-05	0.00648299	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090269	ATCATGGTGTGGGCA[C/T]GCATGCTTTTCCCGT	2177
rs530894323	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10050575	TTGCAGTGAGCCAAG[A/G]TAACACCACTGCACT	2177
rs530932088	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10045754	TTACAGGTGTGTGCT[A/G]CTTTGCCCGGCTAAT	2177
rs530943946	snp	C/T	0.00119737	0.0244387	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092308	GCAGAAACCAAGTGT[C/T]CTGGCTTCCAAAATG	2177
rs530963174	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10061912	ACTCATAGGTGGTAA[C/T]TGAACAATGAGAACA	2177
rs530978757	snp	A/G	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10068008	CTCAGAAAACTGGGT[A/G]TAGATCCATAGCTAC	2177
rs531015348	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10056110	TCTTGAACTCCTCAC[C/G]TCAGGTGATCCGCCT	2177
rs531018822	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098178	CCTTTCTTCACATCA[A/C]CCTTATGAGGCAGAT	2177
rs531055239	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10055629	CATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTT	2177
rs531100506	in-del	-/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10080107	TTAGTAAAGATGGGG[-/T]TTTCACCATGTTGGC	2177
rs531111981	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10028467	GTATTGGCTAGATGT[A/G]AGAGTTGAAATTTGC	2177
rs531130357	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10079842	ACAAAATGAGAAAAT[C/G]TTGGGTCTTGGGTAT	2177
rs531192901	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10033177	GCACTTTGGGAGGCT[C/T]GAGGCAGGCGGATTG	2177
rs531271700	in-del	-/T	0.301177	0.244706	intron-variant	FANCD2	GRCh38.p7	3:10075188	ATTATTATTATTTTC[-/T]TTTTTTTTTTTTGAG	2177
rs531277126	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025003	AGTGATTGAGGCTGC[A/G]ATCGCAGTGGTGCGA	2177
rs531279142	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027715	TCAAGACTATCCTGG[A/G]TAACACGGTGAAACC	2177
rs531304496	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10053282	CTATCGCAAGAACAA[A/G]AAACCGCACACCGCA	2177
rs531334776	snp	C/T	1.64732e-05	0.0028699	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088470	TTGCCAGACAATTCC[C/T]CTGTCGGGTGTGGCC	2177
rs531340070	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095072	TGAGAGGCAAATTAA[A/G]ATGATTATCAGCATA	2177
rs531349460	in-del	-/G			intron-variant	FANCD2	GRCh38.p7	3:10070608	CCCTCTGCCCGGCCA[-/G]CCACCCCGTCTGGGA	2177
rs531370186	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10058917	GCACTGAATCACTTT[C/G]AATGGTATTAGCAAT	2177
rs531412314	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100913	CGTCTCTACCAAAAT[A/T]CAAAAATTAGCCGGG	2177
rs531435666	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10064986	CTCTCGAGACAAATG[C/G]TATTTGGAGAGGTTA	2177
rs531502175	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10064571	TCCCAACCCCAGCAC[C/T]CCTGCACCCTTAGCT	2177
rs531525174	snp	C/T	0.00199481	0.0315187	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092444	GCATTTTTTTTTTTG[C/T]CTTTTCCTTCCTTCC	2177
rs531575421	snp	A/G	0.000164898	0.00907864	intron-variant	FANCD2	GRCh38.p7	3:10066029	GCATAGTTTTTCTCA[A/G]AACTATTTTCTTAGT	2177
rs531580207	snp	G/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026444	GGCCTGGCGGGAAAG[G/T]CGAAAACTACGGGCG	2177
rs531580306	snp	A/G	0.0103295	0.0711199	intron-variant	FANCD2	GRCh38.p7	3:10058288	CTCAGCATCACCCAT[A/G]TATAATTCTGTTTTT	2177
rs531580849	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10042967	TCCTCAGTCTTTCAG[G/T]AGATTGTCATGGTAG	2177
rs531736672	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10031473	CGCCACTGCACTCCA[A/G]CCTGGGCGACAGAGC	2177
rs531787901	snp	A/G	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10038453	GAGGCTCGAAGGAAG[A/G]TGGAAACTATCATAT	2177
rs531835883	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10037648	TTTGTGAAGTGTTCC[A/G]TATATTGAAAAAGAT	2177
rs531840082	snp	A/G	1.64727e-05	0.00286986	missense	FANCD2	GRCh38.p7	3:10065464	GAGAGACAGCATAAC[A/G]GAAACTTGGAGGAGA	2177
rs531847675	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10071982	CCGGGCTTGTCTCGA[A/G]CTCCTGACCTCAAGT	2177
rs531871094	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10089319	AATCACACTGTCCAA[C/T]GTATATAGCTTCCAC	2177
rs531903554	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10045861	CATCTCGGCCTCCCA[A/G]AGTGCTGGGATTACA	2177
rs531937609	snp	A/G	0.00279162	0.0372561	intron-variant	FANCD2	GRCh38.p7	3:10075498	CCCATAGCTTTATTG[A/G]TGCCAAATACGGCAT	2177
rs531943246	snp	C/T	1.65455e-05	0.00287619	synonymous-codon	FANCD2	GRCh38.p7	3:10043562	GTCAGCTATTAGATA[C/T]GAGAAAACCATTTCA	2177
rs531987180	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10071454	CTAAGTGTCCATCAG[C/T]GGGTGAATGGATAAA	2177
rs531990743	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082067	TATCCAACTGCCTAC[A/G]CAACACCTCCTTAGA	2177
rs532009274	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096261	AACATTCAAAGGTTT[C/T]TATAAGAAATGTGAA	2177
rs532037003	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10034053	CTCTGGGCTGGGCAC[A/G]GTGGCTTATGCCTGT	2177
rs532162858	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10062885	AGACGGGGTTTCACC[A/G]TGTTGGGGTTTCGCT	2177
rs532250395	snp	A/G	6.59196e-05	0.00574068	missense	FANCD2	GRCh38.p7	3:10074591	CCCATGCTTTTTTCC[A/G]AGAGCTGGACATTGA	2177
rs532258998	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084891	TGGTTTAAGAAAACA[C/T]TTCTGGCAGCAGAGT	2177
rs532290306	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10069404	CAACATCACTGAGCC[C/T]CAGAGAAATGCAAAT	2177
rs532290437	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098556	GAAACCTGGAGTTGA[C/G]TATCCCTCCTCTAGA	2177
rs532327351	snp	A/T	0.0023933	0.0345097	intron-variant	FANCD2	GRCh38.p7	3:10079263	ATAAAAAAAAAAAAA[A/T]AGGAAGTCTGAAACA	2177
rs532351689	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10075373	TACATTTTTTATAGA[A/G]ACAGGGTTTCACCAT	2177
rs532389664	snp	A/G	4.94686e-05	0.00497311	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092257	ACTTGATAAAGGTGA[A/G]TATGGAGACTGCTTG	2177
rs532391463	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10074049	CTCCCGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG	2177
rs532411498	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10075816	GCTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAC	2177
rs532444624	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10050540	AGGCAGGAGAATGGC[A/G]TGAACCCAGGAGGCG	2177
rs532450327	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085563	CACCCAGCTAATTTT[C/T]GTATTTTTAGTAGAG	2177
rs532473017	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10045733	CAGCTTCCCAAGTAG[C/G]TGGGATTACAGGTGT	2177
rs532541008	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10057548	TTTTGTATTTTTAGT[A/G]GAGACGGGGTTTCAC	2177
rs532570262	snp	A/C	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10035409	AATGTCTGTGTTTTA[A/C]AACTGTGCTTATTAG	2177
rs532605857	snp	G/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097374	TTCACCTCTGCAGTC[G/T]CGACCATAAGAGACA	2177
rs532638263	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10046527	TGTTTCATTGTAGCA[A/T]ATGTACTGATTTGTT	2177
rs532651844	snp	A/G	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10056955	CACCTCCCAGGCTCA[A/G]GCGATCCTCCCATGT	2177
rs532703807	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10050959	GGCATTGTGGTGCAT[G/T]CCTGTAATCCCAGCT	2177
rs532746991	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10077926	ATAGTCCCCGCTACT[C/T]GGGAGGCTGAGATGG	2177
rs532747887	in-del	-/T	0.285834	0.247419	intron-variant	FANCD2	GRCh38.p7	3:10041906	AGAGTCACAGGTCTG[-/T]TTTTTTTTTTGAGAC	2177
rs532765216	in-del	-/T	0.491834	0.0633738	intron-variant	FANCD2	GRCh38.p7	3:10036087	AGAATTATACATTTC[-/T]TTTTTTTTTTTTTTT	2177
rs532783365	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10075243	GCTGGAGTGCAGTGG[C/T]GCGGATCTCCACTCA	2177
rs532834749	snp	C/T			utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101923	CAAATAAATTCTGTT[C/T]TAAGTTCTGCCTCAG	2177
rs532838222	snp	A/G	0.00119737	0.0244387	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090201	CATTTAGAGAGGTAG[A/G]GAAGGAAGCTACTTT	2177
rs532881551	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083691	CAGGAGATCGAGACC[A/G]TCCTGGCTAACACGG	2177
rs532882840	snp	C/G	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100207	TTATTTTATTTACAT[C/G]GTCCCCAGTTTTATT	2177
rs532891398	snp	A/G	1.65094e-05	0.00287305	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093254	AAAGGAGCAGATCTC[A/G]GCCTTGGTTTCTTGT	2177
rs532965786	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10044835	AAATTTACCACCTTG[A/G]CTGCCTGCATACCTA	2177
rs532978698	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10038684	CTTCTGGGTTCAAGC[G/T]ATTCTCCTGCCTCAG	2177
rs533032218	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025938	TAAGGTCACCTTGCC[A/G]GTGGGGGCGAGACGT	2177
rs533060032	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090909	GAGGTGAGGAATGGG[C/T]TCTCTTTTCCTTGGC	2177
rs533084304	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10049792	AAAGTACTATAGATA[C/T]AACAGAGTAAGAATA	2177
rs533219303	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10038046	CCCAGGCTAGAGTAC[A/G]GTGGTGCGATCTTGG	2177
rs533245636	snp	A/G	6.60262e-05	0.00574532	missense	FANCD2	GRCh38.p7	3:10065903	TGGAGCCTGGAGAGA[A/G]GTTGGAGTCCATGTC	2177
rs533281809	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095958	ACAATCTCTGCTCAC[G/T]GCAAGTTCCGCCTCC	2177
rs533298660	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026372	CCGGCCTTCCACTTC[C/T]GGCGCGGAAGTTGGC	2177
rs533330408	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10066779	ACCCAGGCTGGAGTG[C/T]GGTGGCTCAATCTCG	2177
rs533336020	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10055575	CCCAGCACTTTGGGA[A/G]GCTGAGGCGGGCAGA	2177
rs533375153	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10055989	GTTCAAGCAGTTCTC[C/T]TGCCTCAGCCTCCTG	2177
rs533378394	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027255	TGAGGTAAGGGCCCC[C/T]AGGTATACCCTGTGG	2177
rs533411398	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10065290	CAAGACTCTGTCTCA[A/G]AAAAAGAAGTTGTGT	2177
rs533420949	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027674	ACTTTGGGAGTCCGA[A/G]GCGGGCGGATTATGA	2177
rs533451667	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10061886	GTTTTTACCAAACAC[C/T]GCATGTTCTCACTCA	2177
rs533459003	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10072707	ATCTCTGGCCATTTT[A/G]CTATGCCAAAACAAT	2177
rs533488706	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10058378	TTTTTTCTTGTGTTT[C/T]TTGTCCTTTTGGTTG	2177
rs533521006	snp	G/T	0.0023933	0.0345097	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084208	CATCTTGGCCAGGCT[G/T]GTCTTGAACTCCTGA	2177
rs533541893	snp	C/T	0.000115328	0.0075928	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087239	GGAGAAATCAACAGC[C/T]TCTGCTCAGAACAAA	2177
rs533583659	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10033056	TAAATAGAGAGGCAA[C/T]GAAGATTAGAAATCA	2177
rs533623776	in-del	-/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10075639	CATCAGAGAGTAGAA[-/T]TTCTCTAGGTTTAAG	2177
rs533658203	snp	C/G	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10039142	GTATCACTTGTGTGT[C/G]TAGTGCAGTGCCGAA	2177
rs533677406	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093831	TGGATGGTGCCCCAT[C/T]CTTGTCATCTCCTGG	2177
rs533762133	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10080236	TTCTTTGTATTCACT[A/G]TCGGGTCTACTTTTT	2177
rs533849098	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093470	GAAGGCAATGGATGC[A/G]TTTTCCCACCCTAGT	2177
rs533863431	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098332	CTGAAACCACCTCAC[C/T]ATACTGTCCTTTAGC	2177
rs533873544	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10029550	TAGTTCATTTATTGC[C/T]CTTATCTACTCTATT	2177
rs533880685	snp	A/C	0.0103295	0.0711199	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087457	CTAAAATTGCTTAGT[A/C]TGAGTTTGGTTAGAC	2177
rs533938731	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10063080	GATATGCCATGTTTA[C/T]GGAATAACACTTTGG	2177
rs533979084	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10059220	GGTTTTGCCATGTTA[C/T]CCAGGCTGGTCTTGA	2177
rs534027898	snp	G/T	0.00478085	0.0486577	intron-variant	FANCD2	GRCh38.p7	3:10057066	TTGTCATGTTACCCA[G/T]ACTGGTTTGGAACGC	2177
rs534038231	snp	A/G	0.000181191	0.00951644	missense	FANCD2	GRCh38.p7	3:10064775	GGACTGGAAGAATAC[A/G]ACACTCAGGATGGGA	2177
rs534063859	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10024600	AAAAATAAATAGATG[C/T]CTTTCAGTTACAAAT	2177
rs534071764	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10059663	AAAAATTATCCGGGC[A/G]TGGTTGGTGGCGGGC	2177
rs534081946	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10062515	CCAAAGTGCTGGGAG[C/T]ACAGGCGTGAGCCAC	2177
rs534095704	snp	G/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086388	CCCCCTCCCCCTTCA[G/T]TCAGAGTGACTTGGT	2177
rs534184551	snp	A/C	0.00279162	0.0372561	utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101466	TCTTGGCTCACTGCA[A/C]CCTCCATCTCCTAGG	2177
rs534184587	in-del	-/CT			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10089339	ATAGCTTCCACACAA[-/CT]GCCTTGCTCCTCCTC	2177
rs534217132	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025205	AAGCGATCCTCCCAC[C/T]TCAGCCTCCCAAAGT	2177
rs534247470	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10031242	GGCACGGTGGCTCAC[A/G]CCTGTAATCCCAGCA	2177
rs534282043	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10061354	CCCAACCGCCACCGG[C/G]TCAGATAGTCATCAC	2177
rs534306468	snp	C/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10039015	AGAGATGCTGTCTAG[C/T]CCTGTCATCCCTTCT	2177
rs534324594	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097552	TCACCGGCGGTCAGA[A/G]TTTAAGGTTATCTCT	2177
rs534366781	snp	A/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10061937	AGAACACATGGACAC[A/T]GGAAAGGGAACATCA	2177
rs534371152	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10028305	CAGTCCCTAACATAT[A/G]GTATTGAAATCATGA	2177
rs534382676	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10069731	AGCCTCCCGAGGTGC[C/T]GGGATTGCAGACGGA	2177
rs534439949	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093418	GCTCAATTTCTTGCC[C/T]ACAAGCCAGAGTTTC	2177
rs534449980	snp	G/T	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10080865	TGATTAGTTATGATA[G/T]GGCTATATGTCTCAA	2177
rs534478169	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10038908	TTTAAGCACTTACTG[C/T]GTTGATGTTATTAGT	2177
rs534493713	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10072396	CAATTCTCCTGCCAC[A/G]GCCTCCCAAGTAGCT	2177
rs534523335	snp	A/G	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10032047	ATGGGGTTTCACCAC[A/G]TTAGCCAGGCTGGTC	2177
rs534545498	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10066428	GTGCACTTGAATGAG[C/T]TTATTTGATTACCAC	2177
rs534581472	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10044425	ATAATCCCAGCACTT[C/T]GGGAGGCTGAGGCAG	2177
rs534627651	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10078007	CACTGCACATTTAAC[A/G]AAAAAGAAAGAAAAA	2177
rs534677055	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10033559	AGAAAGCAGCTGTAT[C/G]AGTGTCAGAATAATT	2177
rs534708307	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10032631	CATTTTGAATTCTTC[A/G]AATGAAAATAGGTGA	2177
rs534728841	snp	C/G			upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025089	CTCCCGAGTAGCTGG[C/G]ACTACAGGCACACAC	2177
rs534745310	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10079055	AGACCAGCCTGGCCA[A/G]CGTGGCAAGAGCCTG	2177
rs534751086	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085696	CGCCCGACCTCTCAA[A/T]TCTTTTTTCAAACCG	2177
rs534781116	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10080621	ATAAAAAATACAAAA[A/G]CTAGCCATGTTTGTT	2177
rs534792845	snp	A/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10078412	CAGGCTGGAGTGCAG[A/T]GGTGTGATCTCGGCT	2177
rs534794241	snp	A/G	0.000148296	0.00860964	intron-variant	FANCD2	GRCh38.p7	3:10078247	GTGGATTTGGGAACA[A/G]AGGAGGTATTATGAT	2177
rs534806466	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10079393	CACTGCAGCCTCTGC[C/T]TCCTGGGTTCAAGCG	2177
rs534857324	snp	A/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10073112	CCTTTATTAGATTTA[A/T]AAATATACTGTAATT	2177
rs534866660	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083761	AGCGTGGTTGCAGGC[A/G]CCTGTAGTCCCAGCT	2177
rs534992826	snp	A/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10050332	TTGGTGACTGTTAAG[A/T]ATATGTGGCGGTCCG	2177
rs534993394	snp	A/C	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10074238	CATGAACCACCACAC[A/C]TGGCCAGCTCACAGT	2177
rs535022465	snp	C/G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10034219	GTCCCAGCTACTTGG[C/G/T]GGGGCTGAGGCAGGA	2177
rs535025553	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10031586	GAAGAGTAAATTTTA[A/C]ACTTGGCTTCAAGTA	2177
rs535093515	snp	G/T			missense	FANCD2	GRCh38.p7	3:10065446	TTACTGAGACTTTGT[G/T]TGGAGAGACAGCATA	2177
rs535171934	snp	C/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10050440	CCATCCTGCCTAACA[C/T]GGTGAAACCCCGTCT	2177
rs535208098	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082133	GGAATATGTCATCCC[C/T]AGCATGCTCCTTCAG	2177
rs535262063	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088066	TTTATCCCTATTGAT[G/T]AAAAGGGGAAGGTTT	2177
rs535264707	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10035461	ATTTATTCTCTCTGC[A/G]TCTGATTCCTGTTCT	2177
rs535326204	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10080890	TCTCAATCAAACACT[A/G]TTCCTACTCTACAAA	2177
rs535354465	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100940	CGGGCGTGGTGGCAC[A/G]TGCCTGTAATCCCAG	2177
rs535397890	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10036490	TACTGGAGTGTCTTT[A/G]AAGTTTCATCTATTA	2177
rs535413851	snp	A/C/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094581	TCTATTTCTTCTCCA[A/C/G]ATCTGACAGTGGTCT	2177
rs535430892	in-del	-/T	0.00676609	0.0577691	intron-variant	FANCD2	GRCh38.p7	3:10035891	TTGTATTTAATAATA[-/T]TTTTAATTATCTGAT	2177
rs535434932	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10048931	TTAATGTCTTAGAGA[A/C]ACTGTCATAATCCAT	2177
rs535496210	snp	A/G	0.000108317	0.00735845	intron-variant	FANCD2	GRCh38.p7	3:10043915	GACTTAAAAGTAATG[A/G]CATTGGCTAGCTTGC	2177
rs535519043	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10042876	TCTGAAATTTTGGGT[A/G]TGATGTTCTATGACA	2177
rs535519170	snp	A/G	0.000131791	0.00811655	missense	FANCD2	GRCh38.p7	3:10048011	TTGGCAGTCTCCTAT[A/G]CAAATATGCATTTAA	2177
rs535546427	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096112	GGTTATGAAGAGGAA[C/G]TAGAGGTGTTGGTGG	2177
rs535590585	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10053892	AAACATCTCCATCTA[A/G]TGTGAACTTCACGTG	2177
rs535631815	in-del	-/A			intron-variant	FANCD2	GRCh38.p7	3:10079249	CTCTGTCTCAGAAAT[-/A]AAAAAAAAAAAAATA	2177
rs535665764	snp	A/G	0.0103295	0.0711199	intron-variant	FANCD2	GRCh38.p7	3:10033222	TTTGCGACCGGCCTG[A/G]GCAACACGTCTCTAC	2177
rs535736372	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10071123	CACCCAAGAATGATC[A/G]ATAAAAAAAAAAAAA	2177
rs535739628	snp	C/T	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10078377	TTATTTATTTAGAGA[C/T]GGAGTCTCGCTCTGT	2177
rs535772813	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025305	TGCACTCTGCTGCAT[A/G]CTATGGGGTATAGAG	2177
rs535826296	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10056996	AGTAGCTGGGACCAT[A/G]GGTGTGCACCACCAT	2177
rs535838160	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082982	CTGTAATCCCAACAC[G/T]TTGGGAGGCCAAGGT	2177
rs535842006	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090528	GCAGTGGCATGATCT[C/T]GGCTCACTGCAACCT	2177
rs535872780	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10045039	CAGTTAAGATAAGTA[A/G]TAAAATTTTTTTTGT	2177
rs535880276	snp	C/G/T	6.64843e-05	0.00576527	missense	FANCD2	GRCh38.p7	3:10049492	CTATGATGATGAATG[C/G/T]TGTCTTTGTAAAGGT	2177
rs535885275	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10051242	AAAAATTAGCCGGGC[G/T]TAGTGGTGGGCGCCT	2177
rs535900662	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10055117	TTGCTTCAAATCAGC[A/C]ATATAAAACTACTTC	2177
rs535903425	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10043657	GTGACAGATGTATAA[C/T]TGAGGTAGACTGAAA	2177
rs535921825	snp	C/T	0.0103295	0.0711199	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092471	TTCCTCCTACTTATG[C/T]CACAATACTATTTAA	2177
rs535944248	in-del	-/T	0.466768	0.124546	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087282	GATGGGCCTAGATCC[-/T]TTTTTTTTTTTTTTT	2177
rs536044116	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10062037	TGACGAGTTAATGGG[G/T]GCAGCACACCAACAT	2177
rs536045051	snp	A/G	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10059442	AAGATATTATTATTG[A/G]ATGTCTATCATGTGC	2177
rs536056640	snp	A/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10028856	AGAATTAAGGGAGAA[A/T]TATCAGATTTGGGAC	2177
rs536082282	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10059984	ACCAGCCTAGCCAAC[A/G]TGGTGAAACCCCATC	2177
rs536156431	in-del	-/ATGCTTCTGGAATA	0.0023933	0.0345097	intron-variant	FANCD2	GRCh38.p7	3:10076153	TCTGCTTCTAGCAGT[-/ATGCTTCTGGAATA]GTAATATAGCTATTC	2177
rs536166876	snp	A/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10028047	GTGAAACCCTGTCTC[A/T]ACTAAAAAAAAAAAA	2177
rs536180440	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10065267	GCACTCCAGACTGGG[C/T]GACAGAGCAAGACTC	2177
rs536182246	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10034116	ATCACGAGGTCAGGA[A/G]ATCGAGACCATCCTG	2177
rs536186201	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101706	TTCTTAAAGTGGGGT[A/C]TTTATTAACTTGTGG	2177
rs536262348	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086011	AATAACCTGGGTGTC[C/T]TTCAGTAGTTGTAAA	2177
rs536284437	snp	C/T			downstream-variant-500B, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10102206	TGGAGTGCAGTGGCA[C/T]GATCTCAGCTCACTG	2177
rs536308796	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10075430	GACCTCGTGATCACC[C/T]GCCTTGGCCTCCCAA	2177
rs536363733	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10056395	TTTTGAGGAACCACC[A/G]AACTGCTTTCCATAG	2177
rs536369138	snp	C/T	0.00279162	0.0372561	intron-variant	FANCD2	GRCh38.p7	3:10069690	GCCGGTCTCCAGCTC[C/T]TAACCGCGAGTGATC	2177
rs536398064	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092622	CTCACCCACTCCATC[A/G]TGGTTTTGCTCAGCT	2177
rs536436089	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10068282	TTAGATAAATTCAGT[A/G]AAGTTGCAAGATACA	2177
rs536512996	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10073795	ATAGTTTCTGTAAGA[A/G]CCCAAGTTTCATATT	2177
rs536536647	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10033500	ATTAGAAAAAATATT[A/G]TATATTATTTATTTT	2177
rs536566499	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10075490	TGCCCGGCCCCATAG[A/C]TTTATTGATGCCAAA	2177
rs536573929	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10067775	TGCACTCCAGCCTGG[A/G]TGACAGAGCGAGACT	2177
rs536573986	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10074212	GCCTCCCAAAGTCCT[A/G]GGATTACAGGCATGA	2177
rs536655675	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100533	CCTGCAACCATGCCC[A/G]GCTAGTTTTTGTATA	2177
rs536697929	snp	C/T			upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10024642	ATCTTTATAACAGTA[C/T]AAGGACTTATTTTTA	2177
rs536709489	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10046304	GTGATCTGCCCGCCT[C/T]GGCCTCCCAAAGTGC	2177
rs536732710	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10029731	TTTCAATCCCTAACC[A/C]CCCTTCCACCCTTTC	2177
rs536749874	snp	C/T			intron-variant, downstream-variant-500B	FANCD2, FANCD2OS	GRCh38.p7	3:10099706	GAGGTTGTGGTGAGC[C/T]GAGATCATGCTACTG	2177
rs536771350	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10030256	TACATGCCATCATGC[C/T]TGGCTAATTTTTGTA	2177
rs536787122	snp	A/G	0.00993419	0.0697739	intron-variant	FANCD2	GRCh38.p7	3:10055128	CAGCAATATAAAACT[A/G]CTTCACTATTTTATT	2177
rs536811951	snp	A/G	5.03436e-05	0.0050169	intron-variant	FANCD2	GRCh38.p7	3:10043795	TTTCGCTGATGTGTC[A/G]TAATATTTTTGTGAC	2177
rs536824861	snp	A/G	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10031270	GCACTTTGGGTGGCC[A/G]AGGCGGGCAGATCAC	2177
rs536848773	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10077484	TGCTTGAACCTGGGA[C/T]GCAGAGGTTGTAGTG	2177
rs536851242	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10075090	AGCACTTGCATTTCA[C/G]TAGTACATAGAGCAT	2177
rs536855404	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10035030	CCCTTGCAAAGAGCC[A/G]TCTGCTCATTTCTGT	2177
rs536863240	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10038039	TCTGTTGCCCAGGCT[A/G]GAGTACAGTGGTGCG	2177
rs536916590	snp	A/G	0.00159617	0.0282053	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086585	CTCCTGGGCTCAAGT[A/G]ATTGTACTGCCTCAG	2177
rs536926740	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10048727	TCTTCCTGTCATTAA[C/G]AATGTTAAAACGCAT	2177
rs536966845	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10047155	ACTGGATGGGCCAGT[A/G]GTTTGGGGTTTGGGT	2177
rs536983718	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082898	TGACAAAAACTTTGA[A/G]CAATTTATCAAAGAG	2177
rs536988810	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10080155	CTTGACCTCATGATC[C/T]ACCCGCCTTGGCCTC	2177
rs537015333	snp	A/G/T	3.29616e-05	0.00405954	intron-variant	FANCD2	GRCh38.p7	3:10039676	AGGTAGTCTTTCTTT[A/G/T]TTCTGGGTAATGTGC	2177
rs537067657	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026725	GCCTCATCTCACTTC[C/T]GTTGGGCTTTTCTGG	2177
rs537116660	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091833	GGTGCAGTGGCGCAC[A/G]TCTGTAATCTCAGCA	2177
rs537143479	in-del	-/AAT	0.00199481	0.0315187	intron-variant	FANCD2	GRCh38.p7	3:10075718	TACCTTCAGAACAGA[-/AAT]AATAGTATCCTTTTT	2177
rs537148088	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10038790	TTCACCGTGTTGGCC[A/G]GGCTGGTCTTGAACT	2177
rs537245323	snp	A/C	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083738	CTAAAAATACAAAAA[A/C]TTAGCCGAGCGTGGT	2177
rs537256927	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091342	CGCCTCAGCCTCCCA[A/T]AGTGCTGGGATTATA	2177
rs537311400	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10089561	TGCAACCTCCACCTC[C/T]TGGGTTCAAACGATT	2177
rs537359920	snp	C/T	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10054428	ATATACATATATACA[C/T]GTATATACATGTATA	2177
rs537367843	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10050578	CAGTGAGCCAAGATA[A/C]CACCACTGCACTCCA	2177
rs537409017	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10045424	CTGCCCGCCTCGGCC[C/T]CCCAAAGTGCTGGGA	2177
rs537438485	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081602	TAATTTTGTGGGAGT[C/G]TTTTTGTCTGTATTA	2177
rs537451475	snp	A/C	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10078963	AAAAAAAAAGTCTAC[A/C]TGTGCAGTGGTTCAC	2177
rs537455491	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10040228	TTTTTAGTAGAGACG[G/T]GGTTTCACCATGTTA	2177
rs537521795	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10050412	GGCAAATCACGAGGT[C/T]AGGAGATCAAGACCA	2177
rs537538955	snp	C/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086868	GTACATATTAGCGTG[C/G]TGCTTGGGTTTCTCA	2177
rs537583769	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084987	TATTGATAGGGGCCT[A/G]GCCAAAATGATGGTC	2177
rs537599713	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10057733	ACAAAGTCTAATCAT[A/G]TCTTTAGAAGGGGTA	2177
rs537606116	snp	C/G	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10055062	CTTTCCCTTCTTGTT[C/G]TACATCTTAGCTTTT	2177
rs537682377	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10050212	GGGTGGATTGGAGAC[C/T]GCTGAAATGGTCTAA	2177
rs537694913	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10030975	GAATATAGAGAAATT[C/G]GTAGAAAATTTGAAA	2177
rs537700280	snp	C/G	0.00755907	0.0610114	intron-variant	FANCD2	GRCh38.p7	3:10061779	CGCTGCCTTCATGCA[C/G]TTTTATCTTTACCCT	2177
rs537731106	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FANCD2, FANCD2OS	GRCh38.p7	3:10099717	GAGCCGAGATCATGC[C/T]ACTGCACTCCAGCCT	2177
rs537749185	in-del	-/CTC	0.0023933	0.0345097	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094533	CCAAAGTAGGCTGAA[-/CTC]CTCAGGCCCACTCTG	2177
rs537756707	snp	A/G	1.64855e-05	0.00287097	intron-variant	FANCD2	GRCh38.p7	3:10063916	CAAAAGCCCTGGTAA[A/G]GCCAATTGTCTTTTC	2177
rs537766101	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10061279	ACTTTTATACTTTCT[C/T]TAAGAAATCTGCCTT	2177
rs537811863	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10047380	AGCTTAGTACTAAAT[A/G]TAAGATTTTTAAAAA	2177
rs537878728	snp	A/C			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090622	CGCCACCACACCCGG[A/C]TAATTTTTATATTTT	2177
rs537891225	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10048350	CTCTTCATGCCCAGG[C/T]TGGAGTGCAGTGGTG	2177
rs537907921	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025279	GTTTTTTGATGGCCT[A/G]CCATGTGCCTTGCAC	2177
rs537921299	snp	A/C/T	4.94616e-05	0.0049728	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087262	AGAACAAAGAAAAAA[A/C/T]TGGTGATGGGCCTAG	2177
rs537929624	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10046880	TATCTCAATGCAGTT[C/T]GCAACTTTGACAAAC	2177
rs537971180	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10059419	CCTTATAGAAATAAT[A/G]ACAATAAAAGATATT	2177
rs537976850	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10080941	GAAGATGGAGCAAGA[C/T]TTTTATCCCTCTGTC	2177
rs538058982	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083580	CCTTAGGTATTTAAT[C/T]AAGGGAAATGAAAGC	2177
rs538154240	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10036418	TTACTCTGAAAACTA[A/T]TGGTTTCTCTGAAAG	2177
rs538156195	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10057306	AGTGTCCTTTGATGC[A/T]CTAAAGTATTTAGTT	2177
rs538165192	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10036898	TGGAGTGCCGTAGTA[C/T]GATCATGGCTCACTG	2177
rs538181666	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10031016	ATAATATAGGAAATT[A/G]CTGAAAGTAAATGTT	2177
rs538196208	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10059839	TCCCCATTTCACAGA[A/T]GTAAAAATTAAAACT	2177
rs538204189	snp	A/T	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10055819	TCTGTCTCAAAAAAA[A/T]AATAATAATAAATAA	2177
rs538223454	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10062387	CTGGGATTACAGGCA[C/T]GCACCACCACACCCG	2177
rs538250317	snp	A/T	0.000230593	0.0107351	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088909	AGAACTGATCAACTC[A/T]CCTAAAGATGCATCT	2177
rs538267785	snp	C/T	0.00119737	0.0244387	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091921	AACATGGTCAGTATA[C/T]GTTGCAAAGGCTTTT	2177
rs538275825	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10066964	TCCTGGCCTCAAGTG[A/G]TCCTCCTGCCTCAGC	2177
rs538292197	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10056213	ACATTTTGTTTATCC[A/G]TTCATCCATTGATGG	2177
rs538293995	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10050468	TCTCTACTAAAAATA[C/G]AAAAATTAGCCGGGC	2177
rs538303682	in-del	-/T	0.00199481	0.0315187	intron-variant	FANCD2	GRCh38.p7	3:10075933	GACGAGGTTTCACCG[-/T]TGTTAGCCAGGATGG	2177
rs538308069	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084795	GTGCTGGGCCTCAAA[A/G]GTCAGGCAGAATAAT	2177
rs538337145	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092938	CTCAAGTGATCCACC[A/G]GCCTCAGCCTCCCAA	2177
rs538353154	in-del	-/C	0.00398564	0.0444627	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090865	TTTTTTCAAAGAGTT[-/C]CTAGTTTAATTTCCT	2177
rs538385714	snp	C/T	0.00119737	0.0244387	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095461	CTAGAGGGGAATCTC[C/T]GCATCTGAAATTTGA	2177
rs538424074	snp	C/T	0.0103295	0.0711199	intron-variant	FANCD2	GRCh38.p7	3:10070974	CTAATCTCAAGTACC[C/T]AGGGACACAAACACT	2177
rs538464384	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10070890	TAAATGGATTAAGGG[C/T]GGTGCAAGATGTGCT	2177
rs538465710	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10033330	TGCTTGAACCCGGGA[C/G]GTGAAAGTTGCAGTG	2177
rs538497349	snp	C/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10076043	GCCATATCTTTTTTT[C/T]TTTTTTTTAATCTTT	2177
rs538541103	snp	C/T	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10039543	AGAAAAGTTTAAATA[C/T]GAAGAGTAGATATCA	2177
rs538558340	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10028942	CCTCAGTCTCCACAT[C/T]CATAAGAGGAATTAG	2177
rs538561008	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10070188	ACCCTCCGCCCGGCA[A/G]CCGCCCCGTCTGAGA	2177
rs538561093	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10076570	TTTTTAGAGACAGAG[C/T]CTTGCTCTGTCACCC	2177
rs538578323	snp	A/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10032761	TTCCTCTCATGATTA[A/T]TATTCCTGGGTTTAA	2177
rs538650975	snp	A/G	1.648e-05	0.0028705	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098790	ATGACATGTCATCCC[A/G]GGCCTCCAAGAGCAA	2177
rs538688739	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10069660	GTGGAGACGGGGTTT[C/T]GCTGTGTTGGCCGGG	2177
rs538716287	snp	C/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10080009	AACTTCCGCCTCCTG[C/G]GTTCAAGCGATTCTC	2177
rs538732698	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10061996	AGGGGGGAGGGATAG[C/T]ATTAGGAGATATACT	2177
rs538750634	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10040503	AAAATCATTTGTGGA[A/G]CCTATTAAACATCTA	2177
rs538768566	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10075012	CTTTTCACTTTTTCA[C/G]AACATTTGTTCAGCA	2177
rs538785998	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098351	CTGTCCTTTAGCCTC[C/T]GCATGGCCATTCGTG	2177
rs538815281	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10073583	TTTCTAATTATTTTC[G/T]TGACTGTTTTACTCC	2177
rs538842446	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10079429	CCTGCTGCAGCCTCC[C/T]GAGTAGCTGGGGACT	2177
rs538867294	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10046267	ACCGTGTTAGTCAGG[A/C]TGGTCTCGATCTCCT	2177
rs538869047	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10067712	CTGAGACAGGAGAAT[C/T]GCTTGAACCTGGGAG	2177
rs538889530	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10078499	AGCTGGGACTACAGG[A/T]GCCTGCCACCACGCC	2177
rs538951619	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10078914	AGATTGCACCAGTGC[A/C]CTCCAGTCTGGGTGA	2177
rs538969444	in-del	-/A			intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10099459	AGACCCTATCTCCAC[-/A]AAAAAAAATGAAAAA	2177
rs538998482	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097419	GGCCCAGTTCAGAGA[C/T]CTACCCCTAGGTGTG	2177
rs539058185	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10029623	TTGGGAACAGGTGGT[A/G]TTCGGTTACATAAAT	2177
rs539192320	snp	C/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10045879	TGCTGGGATTACAGG[C/T]GTGAGCCACCGTGCC	2177
rs539231356	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10048159	GAAGGAACTCTGACC[A/T]GGGTCTCAAGAAAGC	2177
rs539240944	snp	C/T	0.00318978	0.0398085	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082190	ACCAGTTGCCTGAAC[C/T]AGAAACCAGGAGTTA	2177
rs539268105	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10043276	TATTATATTGTTTTT[C/T]AAATTACATATATGT	2177
rs539291890	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092540	TGCCTTGGATCCTCT[A/T]TGATCTGAGCGCACA	2177
rs539319873	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095415	TTATTCAGAGCAAAT[A/C]CTTAGTTGCTCCTTG	2177
rs539419439	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10044574	CCTGGGCGACAGTGC[A/G]AGACTCCATCTCAAA	2177
rs539533486	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10049635	ATGTGTTAATTCATT[C/G]AGCAAACACTTCTTT	2177
rs539551907	snp	C/T	0.00199481	0.0315187	intron-variant	FANCD2	GRCh38.p7	3:10031314	TGAGACCATCTTGGC[C/T]AACATGGTGAAACCC	2177
rs539582793	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083878	GGGCGACAGAGCAAG[A/C]CTCCGTCTCAAAAAA	2177
rs539612243	in-del	-/A	0.367708	0.220556	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087527	ATGTTCTTCCTTTTC[-/A]AAAAAAAAAAAATTT	2177
rs539654951	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096985	TACAAAAGAGAGAAA[C/T]TTTAAAGCTGGGCGT	2177
rs539706349	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10047611	GATTGCATGGGGAAA[C/G]TGGGATTTAGAACAT	2177
rs539710275	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10054177	TGTTTGTGCCACTGC[A/T]CTCCAGCCAGGGCAA	2177
rs539794023	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10050122	TTTTTAGACAATAAG[A/G]AGCTATTACTAGTTT	2177
rs539814969	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10040981	GGTGGGTCACTTGAG[C/T]CCAGGAGTTTGAGAC	2177
rs539827286	snp	A/G	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10067070	TTTTCTGTATACCAC[A/G]TTGTTGAGGACAGTT	2177
rs539911024	snp	A/C	0.00478085	0.0486577	intron-variant	FANCD2	GRCh38.p7	3:10041214	CAAAAAACAAACAAA[A/C]AAAAAAAAAAGCAAT	2177
rs539922542	snp	A/G	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10040483	CTTAACCCTGGCTGC[A/G]CATTAAAATCATTTG	2177
rs539949942	snp	C/T	0.00119737	0.0244387	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091280	GAGGCGGGGTTTTGT[C/T]GTGTTGCTCAGGCTG	2177
rs539997783	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10053986	GAGGCCAAGGCAGGC[A/G]AATCACATGTGCCCT	2177
rs539997814	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10060674	TTTGCACAAAATGGG[A/G]ACCCTGATTCTTTTA	2177
rs540056452	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092768	GGTGATCACAGCTCA[C/T]TGCAGCCTCAACCTC	2177
rs540101805	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10050953	TACCTGGGCATTGTG[A/G]TGCATGCCTGTAATC	2177
rs540159894	snp	C/G	0.00438332	0.0466095	intron-variant	FANCD2	GRCh38.p7	3:10032480	GGAATGGGGGTGAAG[C/G]GGGGGAGATGGGGGG	2177
rs540221355	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10052254	AACTTGAGCTTTGAG[A/C]TTTTAAGGGAGCTAA	2177
rs540237555	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085188	ATAGGGAATGAAGGA[A/G]AGCTTTTTGCCCTTC	2177
rs540249462	snp	C/T	0.0023933	0.0345097	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10099358	GCTGGCGCAGTGGCT[C/T]ATGCTTGTAATCCTA	2177
rs540349580	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10057912	AGATCTATTAAAGTA[C/T]GGTACACATAAAAAA	2177
rs540419593	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094116	TTAACAGGCCTATTT[C/G]ATTTTTGTATTAAGT	2177
rs540430464	snp	A/G	0.00279162	0.0372561	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085495	CTCCCGAGTTCTAGC[A/G]ATTCTTCTGCCTCAG	2177
rs540458626	snp	A/T	0.0189856	0.0955633	intron-variant	FANCD2	GRCh38.p7	3:10037736	TGTGCACATTAATAA[A/T]TGTAAAAAGAATTAG	2177
rs540460559	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10065010	GAGGTTAGGGAGAAT[A/G]GGGCAGATTCCTTGT	2177
rs540471282	snp	A/C	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10045727	CTGTCTCAGCTTCCC[A/C]AGTAGGTGGGATTAC	2177
rs540496089	snp	C/G	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098451	AGAGTCACCAATACA[C/G]TCTAGCCTTTTAAAA	2177
rs540542282	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10062839	CACAGGCATGCACCA[C/T]CATGCCCAGTTAAAT	2177
rs540555995	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10055917	GGAGTCTCACTCTGT[C/T]GCCCAGGCTTGAGTG	2177
rs540559416	snp	A/T	0.00119737	0.0244387	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092098	GTATAGCTATGTAAT[A/T]CAAGAACTATATCTT	2177
rs540578362	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10046469	GAGTGTGTGGAACAA[A/G]TGAGCATTATCCATT	2177
rs540585887	snp	G/T	0.00398564	0.0444627	intron-variant	FANCD2	GRCh38.p7	3:10069321	TTCGGATTGAAAAAT[G/T]GGTAAAAGGTCTGAA	2177
rs540596455	in-del	-/TTC			intron-variant	FANCD2	GRCh38.p7	3:10040031	ATAGATCCACATACT[-/TTC]TTTTTTTTTTTTTTT	2177
rs540604132	snp	C/T	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10029824	AGTCTCACTCTGTCA[C/T]CCAGGCTGGAGTGCA	2177
rs540682703	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10056515	ATTTCTTTTGATTTT[C/T]ATTAATTAATTAATT	2177
rs540741354	snp	A/T	0.0611083	0.163768	intron-variant	FANCD2	GRCh38.p7	3:10051604	TGTCGAGAAGCATCA[A/T]GGAGGAGAGAATAAA	2177
rs540764870	snp	G/T	0.00119737	0.0244387	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090127	AGGCAATCTTCTTGG[G/T]CTTATTACTGAGTCC	2177
rs540769547	snp	G/T	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086987	AAGATGCTTGAAGAG[G/T]GTTGCTACTAAAGCA	2177
rs540790870	snp	C/T	0.00279162	0.0372561	intron-variant	FANCD2	GRCh38.p7	3:10054208	CAGAGTGAGACTCTA[C/T]CTCAAAATAAATAAA	2177
rs540791491	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10075995	CTTGGCCTCCCAAAG[C/T]GTTGGGATTACAGGT	2177
rs540795198	snp	A/C/G			intron-variant	FANCD2	GRCh38.p7	3:10047772	TGAAGGATTATTTTT[A/C/G]TGTAAAACAAAGATT	2177
rs540805431	snp	C/G	0.000699743	0.0186918	missense	FANCD2	GRCh38.p7	3:10065867	GTTCTCTCTCAGATT[C/G]TCCTATATTCCTAAC	2177
rs540853079	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FANCD2, FANCD2OS	GRCh38.p7	3:10100074	ATGCCTGTGGTCCCT[C/G]CTACACAGGAGGCTG	2177
rs540862844	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10060227	TCTAGCTATATGGCT[C/T]GATATCCATACCTTC	2177
rs540875917	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10068892	AGAATATACATTGGG[A/G]AAAGACACTCTCTTC	2177
rs540903797	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10074298	TGCCTAATAGATCAT[C/G]CCTAAATAGATGACC	2177
rs540907535	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10038143	TTACAGGTGTGCGCC[A/C]CCACACCCAGCTAAT	2177
rs540918839	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10029308	AGTTCAAGACCAGCC[C/T]GGGTAACATAGCGAG	2177
rs540947933	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10031331	ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA	2177
rs540984284	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10054642	GCGCCCGCCACCACG[C/T]CCGGCTAATTTTTTG	2177
rs541080991	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098114	ATATCTGAGTCTTGT[A/G]GTCAATTATATATGA	2177
rs541158285	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097208	ACCGAGGCGAAATTG[A/G]AATTGCTAATGAAGT	2177
rs541186732	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10031437	AACCCGGGAGGCGGA[G/T]CTTGCAGTGAGCCAA	2177
rs541219452	snp	C/T	0.00199481	0.0315187	intron-variant	FANCD2	GRCh38.p7	3:10078603	TTGTGATCCGCCCAC[C/T]TTGGCCTCCCAAAGT	2177
rs541233363	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026339	GTGAGCCCAGCTTAT[C/T]GCCTTCAGCTGGGCT	2177
rs541271054	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10077639	CTGTCCATAATCCCA[A/G]TACCTTGGGAGGCCA	2177
rs541293295	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084052	AGGCTGGAGTGCAGT[G/T]GCGCGATCTCGGCTC	2177
rs541333076	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10071872	TCAAGCAATTCTCCT[C/G]CCTCAGCCTCCTGAG	2177
rs541470290	snp	C/T	1.65214e-05	0.0028741	missense	FANCD2	GRCh38.p7	3:10073289	GCAGCAAGACATCCT[C/T]CTCTGACACACTTTC	2177
rs541477540	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10062095	TGCACGTTGTGCACA[C/T]GTACCCTAAAACTTA	2177
rs541513647	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10075591	GGAGTAGAGGACATT[G/T]TCACAGATAAAGTAA	2177
rs541519297	snp	G/T			intron-variant, utr-variant-5-prime, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026591	GCCCCGAACCTTGGC[G/T]TCCTCATCTGCCCTG	2177
rs541547394	snp	G/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027669	CCAGCACTTTGGGAG[G/T]CCGAGGCGGGCGGAT	2177
rs541649024	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10080985	AGGTTAACAACTCAT[G/T]TCTCCCATCTGCTCC	2177
rs541752166	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100548	GGCTAGTTTTTGTAT[A/G]TTTAGTAGAGACAGG	2177
rs541814762	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10031206	GATTAAGGCTTTATT[A/G]GAAAGAGGGAAAGGA	2177
rs541821674	snp	C/G	0.00755907	0.0610114	intron-variant	FANCD2	GRCh38.p7	3:10070242	AGCCGCCCCATCTGA[C/G]AAGTGAGGAGTCCCT	2177
rs541823267	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10064262	CTTTTTAGAAATGAG[A/G]GAACTGAGACTTAGA	2177
rs541824954	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100809	GCGCAATGGCTCACG[C/G]CTGTAATCCTAGCAC	2177
rs541845596	snp	A/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10058091	TTCTCCAAATACTCC[A/T]TCAGTGTATCCTCTC	2177
rs541884919	snp	C/T	3.32259e-05	0.00407576	intron-variant	FANCD2	GRCh38.p7	3:10064903	TTTCTTTTCTAAACC[C/T]GTTAGTGTTTTGAAT	2177
rs541906102	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10042971	CAGTCTTTCAGGAGA[C/T]TGTCATGGTAGAGAG	2177
rs541939200	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10031359	ATACAAAAAATTAGC[C/T]GGGCGTGGTGGTGTG	2177
rs541958538	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10069874	ATTGCAGCCTCTGCC[C/T]GGCCGCCACCCCGTC	2177
rs542018398	snp	G/T	0.00636936	0.0560724	intron-variant	FANCD2	GRCh38.p7	3:10052872	TCATTAAAAAGTCAG[G/T]AAACAACAGGTGCTG	2177
rs542025893	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10050451	AACACGGTGAAACCC[C/T]GTCTCTACTAAAAAT	2177
rs542028497	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082069	TCCAACTGCCTACGC[A/G]ACACCTCCTTAGATG	2177
rs542049671	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10035304	TCAAGTCTAAATAGC[A/G]GGAACACAGGATAGA	2177
rs542143076	in-del	-/TA			intron-variant	FANCD2	GRCh38.p7	3:10062413	ACCCGGCTAATTTTT[-/TA]TGTTTTTGGTAGAGA	2177
rs542311562	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081901	AGGTACAACATGGAC[A/G]AAAGTAGAACTAAGG	2177
rs542328237	snp	C/G	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10045278	GGTTCACGCCATTCT[C/G]CCGCTTCAGCCTCCC	2177
rs542328402	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10050484	AAAAATTAGCCGGGC[A/G]TCGTGGCGGTCGCCT	2177
rs542336303	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10040973	CTGAAGTGGGTGGGT[C/T]ACTTGAGCCCAGGAG	2177
rs542354866	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10071892	AGCCTCCTGAGTAGC[C/T]GGGACTAGAAGTGTG	2177
rs542368699	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082401	CAGTCCATTCTTCAC[A/G]TGGCAGTAAGAGTGA	2177
rs542414637	snp	C/T	0.00199481	0.0315187	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095548	GCTGGTATATGTTTA[C/T]TTCTGCAAAGTCCTC	2177
rs542442381	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088320	TTGTAAGTTGCCTGT[G/T]AGACCGGGAACGTCT	2177
rs542449623	in-del	-/CTAT	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10052288	GTTTTAGATACCTGG[-/CTAT]CTATGTGTGTCTCTT	2177
rs542484766	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10055855	TAAATAAATAATTCC[A/G]TTCTTTGTTTTTGTT	2177
rs542501883	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027563	TCCTCTTCTCCTACC[C/T]CTTCTACTGGCTAAC	2177
rs542597339	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10079136	GTAGTCCCAGGTACT[C/T]GGGAGGCTGAGGCAG	2177
rs542617214	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093622	CCTTACCAGGCAAAA[G/T]GGAGGAAGGAGGAGT	2177
rs542650475	snp	C/G	0.00199481	0.0315187	intron-variant	FANCD2	GRCh38.p7	3:10040400	CTTAGGATTAGATAT[C/G]TAAATTTGGCCAGTG	2177
rs542681374	snp	G/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10051473	AAGATGGAGGCAGAG[G/T]CTATTGGCTTTGGCA	2177
rs542710779	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084739	CTATCACTGGTGATC[A/C]GGAAGATGCTTCTAG	2177
rs542712397	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092030	TGCAGGCCTCAGAAC[C/T]ATCTTGTGGATGCAC	2177
rs542754825	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10071508	GTACTATTCAGCCAT[A/G]AAAAACAATGAGATC	2177
rs542791021	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10042716	CTTAAGTGCCAATTG[C/T]TCTTCTCTGTCCCCA	2177
rs542795836	snp	A/C	0.00119737	0.0244387	intron-variant, downstream-variant-500B	FANCD2, FANCD2OS	GRCh38.p7	3:10100010	AGACCAACCCGAGAC[A/C]CCATCTCTACAGAAA	2177
rs542797482	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10055499	ATGCATCAGAACTTT[A/T]TTCCCATTACAGCTA	2177
rs542847421	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091620	GCTTACCTCATGCCA[A/G]TTAGCAGGAGGCAAA	2177
rs542904509	snp	A/G	4.25722e-05	0.00461349	intron-variant	FANCD2	GRCh38.p7	3:10067194	AAGTATGAGAATGTA[A/G]TTTGTACTTTGCAGA	2177
rs542909846	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10061701	AAGAAAAAAGAAAAA[A/C]ATATATAGGATAACC	2177
rs542924561	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10079447	GTAGCTGGGGACTAC[A/G]GGCGCGCGCCACCAC	2177
rs542927629	snp	C/T	0.00199481	0.0315187	intron-variant	FANCD2	GRCh38.p7	3:10068090	AGACAAGGATACCCA[C/T]TTATATAATACCACT	2177
rs542950921	snp	A/C	0	0	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097853	AATTACAAAAGTATT[A/C]ATTTGGGGAACTAAT	2177
rs542995851	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10051143	CCCAGCACTTTGGGA[C/G]GCCGAGGTGGGCGGA	2177
rs543035859	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096525	TTATTCTTTGTGACA[A/G]CATCAGATGGCATGT	2177
rs543137453	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10044443	GAGGCTGAGGCAGGC[A/G]GATCATCTGAGGTCA	2177
rs543154820	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10059616	GACCATCCTGGCTAA[C/T]ATGGTGAAACCCCGT	2177
rs543211649	snp	A/G	0.00517822	0.0506191	intron-variant	FANCD2	GRCh38.p7	3:10071266	ATTAGTACAAGCACT[A/G]TGGAGAACAGTTTGG	2177
rs543285661	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10033918	TAGCCAGGATGGTCT[A/T]GATCTCCTGACCTTG	2177
rs543291109	in-del	-/GACTTA			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098431	ACCATGTTCAGCATC[-/GACTTA]GAGTCACCAATACAG	2177
rs543329381	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10036647	CAAGACCAGCCTGGG[C/T]AATGTAGTGAGACCT	2177
rs543356292	in-del	-/A			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096035	ACTCTATTGTTTAAT[-/A]ATCAGTAAAATATAT	2177
rs543396421	snp	A/G	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10060195	AAACAGTTAGTAAAC[A/G]GTAAACGCCTTTATA	2177
rs543432457	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10053571	AAATTAAAAAAAATT[G/T]TTTTGTATTCTCAGT	2177
rs543434944	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10054118	TCAGGAGGCGGAGGT[A/G]GGAGGATCCATTGAG	2177
rs543455922	snp	A/G	0.000132262	0.00813102	synonymous-codon	FANCD2	GRCh38.p7	3:10032932	GCTTCTTAAGATATC[A/G]GGAATTATTCTTAAA	2177
rs543532368	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025764	CTAAAGGATTAACAG[C/T]ACCGTTTTTGTTTTT	2177
rs543608827	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10044202	CTCAGGTCCCTGTAT[C/G]TGCCTAATTGCCCTT	2177
rs543665566	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10077816	AGAAGGATCATCTGA[G/T]CCCAGGAGTTTGAGA	2177
rs543677233	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082352	CCCATTATCTCTCAA[C/T]CTGGACTGGGCTAGG	2177
rs543735825	snp	C/T	0.00318978	0.0398085	intron-variant	FANCD2	GRCh38.p7	3:10076954	TGGGATTTCACCACA[C/T]TGGCCAGGCTGGTCT	2177
rs543808355	snp	A/C/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083271	CAGTGAAGTTAACAC[A/C/G]GAAAATAAACCATCT	2177
rs543815847	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10035877	GTGGATTAACAGTTA[C/T]TGTATTTAATAATAT	2177
rs543837369	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10066694	AACATAACTAGTAAT[A/G]AGTAAAACTAGGGTC	2177
rs543941555	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10080296	TGGAGTGTAGTGGCA[C/T]AATCTTGGCTCACTG	2177
rs543956106	snp	C/T	0.0325976	0.123435	intron-variant	FANCD2	GRCh38.p7	3:10041844	ATTTGATATCTCTCT[C/T]TTTTTTTTTTTTTCC	2177
rs543971169	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10072603	GATTTTAAATGTTTG[C/T]TTTAGTTTTTTTCTG	2177
rs543982528	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10054426	GTATATACATATATA[C/T]ATGTATATACATGTA	2177
rs543989485	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10049685	ATCTCTATTCTGGGT[A/G]CTGTGAATGTAAAGT	2177
rs544005385	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083992	CTAAACTTGTTTCCC[A/G]TGCTTTTGTGTGTGT	2177
rs544084214	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092936	GGCTCAAGTGATCCA[C/G]CAGCCTCAGCCTCCC	2177
rs544087967	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086748	CTAGCAAAGTGCTAG[G/T]ATTACAGGCATAAGT	2177
rs544145440	snp	A/G	0.00478085	0.0486577	intron-variant	FANCD2	GRCh38.p7	3:10049112	AAAGAGGAAAACTAC[A/G]CCAAGGAGCAAAATC	2177
rs544149847	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093514	AAGCCAGTTTTCCTA[C/T]GAATTTGAAAACTTT	2177
rs544154130	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10047719	AATTATTATCCAAAC[A/G]TGGAATCCCATTGAT	2177
rs544291582	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081814	TTCCATGATACCTTC[A/G]TGGAAACAGTGGGAC	2177
rs544294179	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10056009	TCAGCCTCCTGAGTA[G/T]CTGGGATTATAGGCA	2177
rs544322710	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10042917	TATTCTCATAACTCT[A/G]TTTTTCAAAATGTCC	2177
rs544399792	in-del	-/AATA	0.00279162	0.0372561	intron-variant	FANCD2	GRCh38.p7	3:10055826	CAAAAAAAAAATAAT[-/AATA]AATAAATAAATAAAT	2177
rs544407730	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10079579	AATCCGCCCACCTCG[A/G]CCTCCCAAAGTGCTG	2177
rs544424828	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088262	TAGGCAAATGAGTTT[A/G]TGTCTGGCAAAAGGG	2177
rs544426876	in-del	-/CAA	0.00159617	0.0282053	intron-variant, downstream-variant-500B	FANCD2, FANCD2OS	GRCh38.p7	3:10099757	AGTGAGACTCCGTCT[-/CAA]CAACAACAAAAAAGT	2177
rs544471843	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10058056	AGATCATTTTTCTTC[C/T]AGGGATGTACTTCTT	2177
rs544533851	snp	A/G	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10040074	CAGTCTTGCTCTGTC[A/G]CCCAGGCTGGAGTGC	2177
rs544536219	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10051065	CACTCCAGCCTAGGC[A/G]AGAAGAGCGAAACTG	2177
rs544539806	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086153	ATCAGCCCATAAACT[C/G]AGCCTTTTCAAGTAA	2177
rs544563396	snp	A/G	0.00279162	0.0372561	intron-variant	FANCD2	GRCh38.p7	3:10050351	TGTGGCGGTCCGGGT[A/G]CGGTGGCTCATGCTT	2177
rs544587595	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091737	ATCCTGAATCTCAGA[A/G]ACTCAAAACAAAACA	2177
rs544598972	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10064207	TTTTATGCACTCTCT[C/G]TTTTCTACTTCACAA	2177
rs544637618	snp	G/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10044838	TTTACCACCTTGGCT[G/T]CCTGCATACCTATTT	2177
rs544676880	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087711	GGAGTGCAGTGGTGC[A/G]ATGTTGGCTCACTGC	2177
rs544697633	in-del	-/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088425	TTCCCATATGTAAGA[-/T]TCCTTTGTCTTCTTT	2177
rs544699784	snp	A/T	0.0134861	0.0810011	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094707	CTCAGAAATGATTTT[A/T]AAAAAAAAAAAGCTC	2177
rs544778144	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10035916	TCTGATTATTTTAAC[A/G]TTGCCTTGATAATCA	2177
rs544797360	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10049855	TCAAAGAGGCAATGT[C/G]AGTGATTGCTGAAGG	2177
rs544799101	in-del	-/T	0.430736	0.176369	intron-variant	FANCD2	GRCh38.p7	3:10052522	ATATGTTGGGAAAGA[-/T]TTTTTTTTTTTTTGA	2177
rs544811421	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101062	GACAGAGCAAGACTC[C/T]TTTAAAAAAAAAAAA	2177
rs544820499	snp	A/C/G	0.00199481	0.0315187	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084139	GCTGAGATTACATGC[A/C/G]CCTGCCACTGCACCT	2177
rs544849970	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10063503	GTAAAGCAATACATT[G/T]TTATTTCATTCTTTA	2177
rs544879199	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10069747	GGGATTGCAGACGGA[A/G]TCTGGTTCACTCAGT	2177
rs544897390	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10065163	GCAGTGTGGCATGCA[C/T]CTATAATCCCAGCTA	2177
rs544902101	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10032105	CTGCCTCGGCCTCCC[A/C]AAGTGCTGGGATTAC	2177
rs544908349	snp	C/T	0.000150357	0.00866925	intron-variant	FANCD2	GRCh38.p7	3:10060409	CGGCAGACAGGTACA[C/T]GTGGAGATTCTGACT	2177
rs544961451	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098541	GCCACAGACATCTCA[A/G]AAACCTGGAGTTGAG	2177
rs544972810	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026405	CACGTCATGGCGCGC[C/G]TCGGTGGCGTCAGAG	2177
rs545034053	snp	A/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10045261	GCAAGCTCCGCCTCC[A/T]GGGTTCACGCCATTC	2177
rs545076116	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10037256	AAGTTCAATTTTGTT[A/C]GCAATCAAAGGCACA	2177
rs545110166	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097705	TATATACCTCCTTCT[C/G]GGCTGACAGGATTAA	2177
rs545138031	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091588	CTGCCAAGATCCACA[A/G]TATCTCAAACAGGCT	2177
rs545182609	snp	G/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10060879	GGGGGCTTGATAAGA[G/T]GTTGCCATTACAAAC	2177
rs545190433	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10068553	GAATTAATATTGTTA[A/G]AATTTCCATGCTACC	2177
rs545245589	snp	G/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10040339	CCGTGCCTGGCCCCA[G/T]GTACTTTCTTTTAAA	2177
rs545267015	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10078646	GGCATGAGCCACCGC[A/G]CCCGGCCTCATCTTG	2177
rs545281785	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10072526	TCAGGTGATCCGCGC[A/G]CCTTGACCTCCCAAA	2177
rs545284454	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027676	TTTGGGAGTCCGAGG[C/T]GGGCGGATTATGAGG	2177
rs545320094	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026911	GTAAATGTTAACCAT[G/T]ATTAGAAGTCATTAT	2177
rs545327078	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10079105	AAAAATTAGCCAGGT[A/G]TGGTGGCGCATGCTT	2177
rs545350482	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10077174	GGAGGTTGAGGCTGC[A/G]GTGAGCTGTGAACAC	2177
rs545353445	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101322	TGATCATTTTGTGTT[A/G]GAGTTTGAAATCCGC	2177
rs545440920	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10067956	TGATGCTTAAAAAAA[A/T]TTTATAAAATTCAAC	2177
rs545449902	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10050561	CCAGGAGGCGGAGCT[C/T]GCAGTGAGCCAAGAT	2177
rs545515529	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10028407	TCCTTCAGCAACAGC[A/G]AAGTAGTCTGCCTAA	2177
rs545536805	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10070308	CGTCTCCGCCCGGCA[A/G]CCACCCCGTCCGGGA	2177
rs545556102	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10029034	CTGTACCCTTAAAAA[A/G]CTTTATGGTCTTTCT	2177
rs545571165	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095475	CCGCATCTGAAATTT[C/G]ATTCAAACTCCAAAG	2177
rs545598171	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10064944	AATTCCACAGCTCTT[G/T]GTGGGGAAGTTGAGT	2177
rs545659833	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081010	TGCTCCTACCTGGTG[A/G]CACAGGTTTGACTTG	2177
rs545763481	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10065311	GAAGTTGTGTTCCCT[A/G]TGTATGTGGAGTAAT	2177
rs545780254	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10051792	TTCCTCAGACAAACC[A/G]TGAAAGGTAGTATAG	2177
rs545805202	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10038940	TCTTACCTTTTAAAA[A/C]TACTTGTCATATTCA	2177
rs545808241	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094985	AAAATGCAGGTCTTA[C/T]AACTCTCAGATTGAT	2177
rs545809874	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10058981	TCTTTCCATTTCCTT[A/G]TGTCTTTAATGTTTT	2177
rs545828464	in-del	-/T	0.142947	0.22592	intron-variant	FANCD2	GRCh38.p7	3:10045602	ACAAAGTAATTTTCC[-/T]TTTTTTTTTTTTTTT	2177
rs545846217	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10053153	ACAATGATAGACTGG[A/C]TTAAGAAAATGTGGC	2177
rs545951075	in-del	-/TTC			intron-variant	FANCD2	GRCh38.p7	3:10056491	AACATGTATTTTCCT[-/TTC]TTAAAAATTTCTTTT	2177
rs545971295	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10069922	CTCTGCCTGGCCGCC[C/T]ATCGTCTGGGATGTG	2177
rs545987400	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10030771	TGGGCGTGGTGTCAC[A/G]TGTCTGTAATCTCAG	2177
rs545989387	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10036079	TTGGAAAGAGAATTA[A/T]ACATTTCTTTTTTTT	2177
rs545995277	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10042896	GTTCTATGACATTGC[A/G]TTGGCTATTCTCATA	2177
rs546037631	snp	A/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10048490	TTGTATTTTTAGTAG[A/T]CACAGCGTTTCACCA	2177
rs546107174	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10042426	AAAAATCTAAAATTT[C/T]GTTTTTCCCTAAATT	2177
rs546227562	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10089224	TGGGAGGCGGAGGTT[A/G]CAGTGAGCCGGGATC	2177
rs546272652	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10068241	TCTTATATTTGGAAA[A/G]GCCTAAAGACTCCAC	2177
rs546290687	snp	A/C	0.0494327	0.149241	intron-variant	FANCD2	GRCh38.p7	3:10077129	TCCCAGCTACCTGGG[A/C]GGCTGAGGTGGGACC	2177
rs546351552	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10039471	TTTCCATCCATCCAT[A/T]AGCTTTTTCCAATTT	2177
rs546420685	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10049062	CTTGTACAACCTCAA[C/T]CTAAAGGGTAAAATT	2177
rs546426417	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10066925	ACATGGGCTTTCACC[A/G]TGTTGGCCAGACTGG	2177
rs546427659	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082449	CAGTTTGATCCTATC[C/G]CAATTTTGATTTCTG	2177
rs546598755	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10080525	CCTTTAACCCCAACA[C/G]TTTGGGAGTCCAAGA	2177
rs546601760	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10050379	CTTGTAATCCCAGCA[A/C]TTTGGGAGGCCAAGG	2177
rs546641313	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10073533	TTCAGATTAGACTTC[A/G]GGTCCTTATTCCTGC	2177
rs546657500	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10033297	TCCCAGCTGCTTGGG[C/T]GCCTGAGTCAGGAGA	2177
rs546681933	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10028518	GCATTAATATGGAGA[C/T]GTGAGCCCCTCTGAT	2177
rs546691739	in-del	-/TCT	0.00159617	0.0282053	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082515	TACCTAGCCTCTAGG[-/TCT]TCTTCTGACTCCTGC	2177
rs546726120	snp	A/G	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10050391	GCACTTTGGGAGGCC[A/G]AGGCGGGCAAATCAC	2177
rs546822754	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10080724	TGCAGTGAGCTGTGA[C/T]CGTGCCACTGCACTC	2177
rs546884259	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10036005	TGAAGACATATTCGT[A/G]TGGATATCCTTGTAA	2177
rs546901131	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084443	TGCAGGCATGTACCA[C/G]CATGCCCAGCTGATT	2177
rs546962411	snp	C/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10078447	GCAAGCTCCGCCTCC[C/T]GGGTTCATGTCATTC	2177
rs547061132	snp	A/G	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10042064	CACCACTCCCGGCTA[A/G]TTTTTGTATTTTTAG	2177
rs547064803	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10034852	CTGTTTTGCCAACTT[C/T]ATGGGGCTGGGGAGG	2177
rs547132561	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082746	AGTTCTCTTCTAACA[C/T]TCTGGTATCCGTTCG	2177
rs547136922	snp	G/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093047	CCTCTAATAATGCCA[G/T]CTTCTCAACACTCCC	2177
rs547150617	in-del	-/TT			intron-variant	FANCD2	GRCh38.p7	3:10072295	CTTTTTTTTTTTTTT[-/TT]GAGACAGAGGCTTGC	2177
rs547166347	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10050852	AGCACTTTGGGAGGC[C/T]GAGGCGGACGGATCA	2177
rs547172707	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10040196	CCTGCTACCATGCCC[A/G]ACTAATTTTTTTGGT	2177
rs547204364	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088651	GGAATTTGAAAACAA[C/T]GAAGTAGGTTAAAAA	2177
rs547227726	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095349	TTGGGGGATCCATGG[A/G]CTACCATCCTTCTTC	2177
rs547268740	snp	A/G	0.0023933	0.0345097	intron-variant	FANCD2	GRCh38.p7	3:10046147	TAAGCTCTGCCTCCC[A/G]GGTTCACGCCATTCT	2177
rs547272282	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10053309	CGCATATTCTCAGTC[A/G]TAGGTGGGAATTGAA	2177
rs547298856	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10059192	CTAATTTTTGTATTT[C/T]CTATAGAGATGAGGT	2177
rs547311009	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098654	GCCTGTAAACTCAAC[C/T]TTCTCCCCTATTACC	2177
rs547311846	snp	A/G	1.64746e-05	0.00287002	missense	FANCD2	GRCh38.p7	3:10048019	CTCCTATACAAATAT[A/G]CATTTAAGTTTTTTG	2177
rs547461626	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10037947	GTCATTTTTATGTTC[C/T]CCTTTTTAATTTTTT	2177
rs547493630	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10048597	GGCGTGAGCCATTGG[A/G]CCTGGCCGAGACACA	2177
rs547520016	snp	A/G	0.00159617	0.0282053	downstream-variant-500B, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10102342	TAGAGACAGGGTTTC[A/G]CCATATTGACCAGGC	2177
rs547570520	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027096	AAACAGTTCTTGTTA[A/G]CTTTTAGCATTTCCC	2177
rs547584450	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095929	CTTTGTAGCCCAGGC[C/T]GGAGTGCAGTGGCAC	2177
rs547584790	snp	C/T	0.299158	0.245119	intron-variant	FANCD2	GRCh38.p7	3:10054378	ATATACGTGTATATA[C/T]ATATATATATGTATA	2177
rs547643531	snp	C/T	0.00318978	0.0398085	intron-variant	FANCD2	GRCh38.p7	3:10063093	TATGGAATAACACTT[C/T]GGTTGAAGCATGGGG	2177
rs547765481	snp	A/T	0.00398564	0.0444627	intron-variant	FANCD2	GRCh38.p7	3:10054854	ACATTTTTTTTAATT[A/T]AAAAAAAAACTTTTG	2177
rs547781390	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10075052	TGCTTACTGAGTCCT[A/G]TTTTGTGTTTGCCAC	2177
rs547803490	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10050063	TAGGACAGGCCCATG[C/T]TGCAAAGAGTCTCAA	2177
rs547806425	snp	A/G	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10079431	TGCTGCAGCCTCCTG[A/G]GTAGCTGGGGACTAC	2177
rs547864649	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10066750	GTTTTTTTGAGACAG[A/G]GTCTTGCTCTGTCAC	2177
rs547875752	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10057621	GCCTGTCTCAGCCCC[G/T]CAAAGTGCTGTGATT	2177
rs547880758	snp	C/T	0.0103295	0.0711199	intron-variant	FANCD2	GRCh38.p7	3:10054366	ACGTATATATATATA[C/T]ACGTGTATATACATA	2177
rs547890112	snp	A/G/T	0.00119737	0.0244387	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093791	GGAGAATGCTACTTC[A/G/T]CCACTCCTCAAGTTT	2177
rs547919930	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10061134	CAACTTTGGCATTAT[C/G]AGTACTGCACAAAGC	2177
rs547941332	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10031556	AGGAAAAAACAAAAT[A/G]GCATCATTAAGGGAG	2177
rs547960516	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10072125	TACTGTACATTTAAA[A/C]ATAACTAAAATAGTA	2177
rs547976333	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026601	TTGGCTTCCTCATCT[A/G]CCCTGAGATGGGATA	2177
rs547983650	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10077525	ATGCCACTGCCCTCC[A/G]GCCTGGGTGACGGAA	2177
rs548022100	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10029450	AGGGTGCAATGAGTC[A/G]ATAACAGCACCACTG	2177
rs548037882	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10077916	GTGTGTGCCTATAGT[A/C]CCCGCTACTCGGGAG	2177
rs548092979	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10038626	GGCTCTGTCACCCAG[C/G]CTGGAGTGCAGTGGC	2177
rs548168277	snp	A/G	8.23662e-05	0.00641688	intron-variant	FANCD2	GRCh38.p7	3:10064686	TCCCTGTAGCCTTGC[A/G]TATTCCTGAGCTGCA	2177
rs548255173	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10099412	AGGATTGCTTGAGTC[C/T]GGGAGCTCAAGGCAA	2177
rs548259902	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10062982	CTGGGATTACAGATG[G/T]GAGCCACCACTCCCA	2177
rs548260067	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10069509	GTCTCCCTCTGATGC[C/G]GAGCCAAAGCTGGAC	2177
rs548361197	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10075978	CCTCGTGATCCGCCC[A/G]CCTTGGCCTCCCAAA	2177
rs548395474	snp	G/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10069156	ACAAATGGGATCACA[G/T]TAAGTTAAAAAGTTA	2177
rs548423041	snp	C/G	0.00755907	0.0610114	intron-variant	FANCD2	GRCh38.p7	3:10070145	GAGGAGCGTCTCTGC[C/G]CGGCTGCCCCGTATG	2177
rs548428722	snp	C/T	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10074223	TCCTGGGATTACAGG[C/T]ATGAACCACCACACC	2177
rs548481168	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10034206	AAACGTGTCTGTAGT[A/C]CCAGCTACTTGGGGG	2177
rs548553183	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10070410	CCCGGCCAGCTGCCC[C/G]GTCCGGGAGGTGAGG	2177
rs548605189	snp	A/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10031250	GGCTCACGCCTGTAA[A/T]CCCAGCACTTTGGGT	2177
rs548647514	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10077917	TGTGTGCCTATAGTC[C/G]CCGCTACTCGGGAGG	2177
rs548688468	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10076448	TGAATTATTATTTTA[C/G]TATTCTGAATATTTA	2177
rs548693888	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10073049	TTAACCTAAAAGTTA[G/T]GTGTATCATGGCATC	2177
rs548832619	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10078690	GTCTGAAGGCTGGGC[A/G]TGGTGGCTCACGCCT	2177
rs548876750	snp	A/G	0.000399281	0.0141238	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087145	ACAGCCAGAGCGTCC[A/G]TTACTTGCAGAATTT	2177
rs548887691	snp	A/T	0.000264157	0.0114895	intron-variant	FANCD2	GRCh38.p7	3:10052380	GTTGGCATCATTTTT[A/T]CCACAGGGCATTTTA	2177
rs549008438	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10054800	AACCATCATATTTTT[A/T]ATCTTTTTTTCCCCC	2177
rs549027445	in-del	-/A	0.00279162	0.0372561	intron-variant	FANCD2	GRCh38.p7	3:10061021	GGGAGCAAAGAAAGC[-/A]AAGACAAAGTATGTA	2177
rs549039936	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027446	AAGGTTCTGATTTAC[A/G]AGATTAAAAGGTCAT	2177
rs549045678	snp	A/G	0.00159617	0.0282053	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083749	AAAAATTAGCCGAGC[A/G]TGGTTGCAGGCGCCT	2177
rs549079987	snp	A/G	1.69735e-05	0.00291315	missense	FANCD2	GRCh38.p7	3:10039280	TCCTAACATTTTAGC[A/G]AGAACAGTGATGAAA	2177
rs549109808	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085637	CCTCGTTATTCGCCC[A/G]CCTCAGCCTCCCGAA	2177
rs549140674	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10062265	TTTTTTTTTTTTAGA[A/G]AGTCTCGCTCTGTCA	2177
rs549162099	snp	A/G	0.00159617	0.0282053	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084348	CCAGGCTGGAGTGTA[A/G]TAACACAATCACAGC	2177
rs549223151	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10054363	TATACGTATATATAT[A/G]TATACGTGTATATAC	2177
rs549230330	snp	A/G			intron-variant, utr-variant-5-prime, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026617	CCCTGAGATGGGATA[A/G]TCCCCACAGGTACCT	2177
rs549325115	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098597	CAAGTTGGTATCCAT[A/G]TTTGCTGTGTTTTGA	2177
rs549347680	snp	G/T	0.00438332	0.0466095	intron-variant	FANCD2	GRCh38.p7	3:10056116	ACTCCTCACCTCAGG[G/T]GATCCGCCTGCCTCG	2177
rs549360040	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10079365	GCTGGAGTGCAGTGG[C/T]GCAATCTCGGCTCAC	2177
rs549383233	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090741	GAGATTACAGACGTG[C/T]GCCACTGCGCCCGGT	2177
rs549386689	snp	A/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10040685	TTTCCATCTTAATGC[A/T]ACTTTTTATTGTACT	2177
rs549387907	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10045832	GTCTTGAACTCCTGA[C/G]GTCGTAATCCACCCA	2177
rs549444424	snp	A/T	0.00159617	0.0282053	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095106	TGGAAACTGCAGAGT[A/T]TATCCTCTTTGGAGC	2177
rs549444572	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087918	TCCCAAAGTGCTGGG[A/T]TTACAGACGTGAGCC	2177
rs549477710	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10069886	GCCCGGCCGCCACCC[C/T]GTCTGGGAAGTGAGG	2177
rs549500675	snp	C/G	0.00398564	0.0444627	intron-variant	FANCD2	GRCh38.p7	3:10050591	TAACACCACTGCACT[C/G]CAGTCTGGGCGACAG	2177
rs549507467	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098223	ATAAAAATTGAAGCT[C/T]AGAGAAGTTAAGTAA	2177
rs549507714	snp	A/G	0.00031295	0.0125051	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088476	GACAATTCCTCTGTC[A/G]GGTGTGGCCAAGTGG	2177
rs549514385	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082096	GATGTGGCATTGACA[C/T]CTCACACTCCACATC	2177
rs549543128	in-del	-/ATTTATTGTAT	0.00557542	0.0525036	intron-variant	FANCD2	GRCh38.p7	3:10073758	TGTTGATCAGCCACC[-/ATTTATTGTAT]ATTTATTAGGTATAG	2177
rs549581431	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094523	ACTGAATATTCCAAA[A/G]TAGGCTGAACTCCTC	2177
rs549605161	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10079186	GAGGCAGACGCTGCA[A/G]TGAACCAAGATCATG	2177
rs549638847	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10070112	GCCTCTGCCCGGCCG[C/T]GACCCCGTCTGGGAG	2177
rs549663714	snp	A/G	0.00557542	0.0525036	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100926	ATACAAAAATTAGCC[A/G]GGCGTGGTGGCACAT	2177
rs549674160	snp	A/C/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10044621	GATTGAGTTCCTTAG[A/C/G]TGCTGATTGGTTGCC	2177
rs549676773	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027730	GTAACACGGTGAAAC[C/T]CCGTCTCTACTAAAA	2177
rs549686295	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10058318	TCATCGCTGGCACCA[C/T]GAAGGTTGCCACTCC	2177
rs549728823	snp	A/C	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026445	GCCTGGCGGGAAAGT[A/C]GAAAACTACGGGCGG	2177
rs549790164	snp	C/G/T	0.000115314	0.00759241	missense	FANCD2	GRCh38.p7	3:10047987	CTCTAGACCAGAGTA[C/G/T]AATTTCATTTGGCAG	2177
rs549812079	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10059093	ATCCTGGCTCACTGT[A/G]TTCTTGACTTCCCAG	2177
rs549839521	snp	C/T	0.00279162	0.0372561	intron-variant	FANCD2	GRCh38.p7	3:10031480	GCACTCCAGCCTGGG[C/T]GACAGAGCAAGACTC	2177
rs549843976	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10064574	CAACCCCAGCACCCC[A/T]GCACCCTTAGCTCCA	2177
rs549848489	in-del	-/A			intron-variant	FANCD2	GRCh38.p7	3:10077072	TCTCTACAAAAAGTT[-/A]AAAAAAAAAAAGTAG	2177
rs550023441	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10063976	ACTACACTCTTCAAG[C/T]CTTTCTGTTGCAGTG	2177
rs550025616	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10042997	GAGAGACTGGACTGT[A/G]CCTACCCACTATGAA	2177
rs550075536	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10030789	TCTGTAATCTCAGCT[A/G]CTCGGGAGGCTGAGG	2177
rs550125193	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10029372	TGGGCATGGTGGTTT[G/T]TGCCTGTGGTCCCAG	2177
rs550139381	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10056281	ATGTTGCTGTGACCA[G/T]TGGTTTACAAATATT	2177
rs550171751	snp	A/G	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10076587	TTGCTCTGTCACCCA[A/G]GCTGAAGTGCAGTGG	2177
rs550216312	snp	A/G	0.00119737	0.0244387	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096738	AGTCAGACCAGTACA[A/G]ACCTCTCTCCACAGC	2177
rs550225055	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10036980	GCCTGGGACTACAGG[C/T]GTGCGCCACCCGGTC	2177
rs550273149	snp	C/G	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10072048	TACAGGCATGAGCCA[C/G]AGAGCCCAGCCAAGA	2177
rs550273287	snp	C/T	0.000164723	0.00907383	synonymous-codon	FANCD2	GRCh38.p7	3:10065484	CTTGGAGGAGATTGA[C/T]GGTCTACTAGGTATG	2177
rs550303875	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10062886	GACGGGGTTTCACCA[C/T]GTTGGGGTTTCGCTA	2177
rs550336059	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10066032	TAGTTTTTCTCAAAA[C/T]TATTTTCTTAGTTCC	2177
rs550387115	snp	A/G	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10071516	CAGCCATAAAAAACA[A/G]TGAGATCCTGTTGTT	2177
rs550414950	snp	C/T	0.0023933	0.0345097	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082642	ATTCTCCTGCCAGGA[C/T]CCCCACTCTTCTTGA	2177
rs550457227	snp	A/G	0.000162324	0.00900755	intron-variant	FANCD2	GRCh38.p7	3:10040572	GTCCTGCATCAGACC[A/G]CTTGCGGAGACCCAT	2177
rs550526105	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10036165	AATCTCGGCTCACTG[C/T]AATCTCTGCCTTCCC	2177
rs550571186	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10075826	AGCTCCGCCTCCCGG[A/G]TTCACACCATTATCC	2177
rs550573437	snp	C/T	0.00279162	0.0372561	intron-variant	FANCD2	GRCh38.p7	3:10069667	CGGGGTTTCGCTGTG[C/T]TGGCCGGGCCGGTCT	2177
rs550583879	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085592	AGACGGGATTTCACC[A/G]TGTTGGCCAAGATGG	2177
rs550600518	in-del	-/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10051136	CTGTAATCCCAGCAC[-/T]TTGGGAGGCCGAGGT	2177
rs550613588	snp	A/C	0.00279162	0.0372561	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10099377	CTTGTAATCCTAGCA[A/C]TTTTTGAGGCCAAGG	2177
rs550616782	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10045739	CCCAAGTAGGTGGGA[C/T]TACAGGTGTGTGCTA	2177
rs550623174	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10068275	AAAACTATTAGATAA[A/G]TTCAGTAAAGTTGCA	2177
rs550649587	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10079265	AAAAAAAAAAAAATA[A/G]GAAGTCTGAAACAGA	2177
rs550651445	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10035416	GTGTTTTAAAACTGT[A/G]CTTATTAGCCTAATA	2177
rs550705053	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10031433	CATGAACCCGGGAGG[C/T]GGAGCTTGCAGTGAG	2177
rs550710219	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10075388	GACAGGGTTTCACCA[C/T]GTTAGCCAGGATGGT	2177
rs550753330	snp	C/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10051679	TAGATGAGGAGGTTT[C/G]AGATTGCTTGTAGGC	2177
rs550814029	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10042117	TGTCCAGGCTGGTCT[G/T]GAACTCCGGACCTTG	2177
rs550834524	snp	A/G	0.00517822	0.0506191	intron-variant	FANCD2	GRCh38.p7	3:10055572	AATCCCAGCACTTTG[A/G]GAGGCTGAGGCGGGC	2177
rs550863750	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10051211	CGGTGAAACCCCGTC[C/T]CTACTAAAAATACAA	2177
rs550914405	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087077	CATGTGGATTTAAAT[A/G]TATCTGTGACACATA	2177
rs550943856	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10073685	TACATTTGTACTGTT[C/T]GTAGAATGAGTTTCA	2177
rs550957261	snp	C/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10056957	CCTCCCAGGCTCAAG[C/T]GATCCTCCCATGTCA	2177
rs550973745	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10072142	TAACTAAAATAGTAT[A/G]ATTGGATTGTTTGTA	2177
rs550991369	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10036198	GGTCCAAGAGGTTCT[C/T]GTGCCTCAGCCTCCC	2177
rs551095369	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085735	TTGATGGTACAGACT[A/G]GAGGCCAGGATCCTT	2177
rs551110726	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10077930	TCCCCGCTACTCGGG[A/G]GGCTGAGATGGGAGG	2177
rs551153785	snp	A/G	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10054337	CTTTGAACAACCAGC[A/G]TATATATATATATAC	2177
rs551186571	snp	A/G	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10041387	GTTCTCTGGGTAGTG[A/G]GGATTGTGATGGAAG	2177
rs551229916	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10059730	AGAATGGCATGAAGC[C/T]GGGAGGTGGAGCTAG	2177
rs551268802	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10053798	TCTGTTAGGGTAGAG[A/G]TGGGTCTGTGATCAG	2177
rs551278018	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10048685	GCAAGTAAAGAACAG[C/T]GTCTTATTTTGTATT	2177
rs551298703	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086473	TTATCATCCCTGTCT[A/G]TAGGTCAGGACCTTA	2177
rs551310765	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082797	TTATTATAATTACTT[G/T]TTCATCAGTCTTTCC	2177
rs551316635	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10043770	GGCATGCTGAATAAG[G/T]TGTAACGTGTTTCGC	2177
rs551320998	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083715	AACACGGTGAAACTC[C/T]GTCTGTACTAAAAAT	2177
rs551349008	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10038751	GTGCCCAGCTAATTT[C/T]TGTATTTTTAGTAGA	2177
rs551482269	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10029086	TTATGATCTAGACAC[A/G]TGCTATGTTAGTGAT	2177
rs551554725	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10089336	TATATAGCTTCCACA[C/T]AACTGCCTTGCTCCT	2177
rs551590907	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097491	TCAGTGATATTTCTC[C/T]CATTTGCTTTTGAAG	2177
rs551618155	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086289	GCCTGTTTCTTTCCC[C/T]TTGTCTTGTAGGAAG	2177
rs551625429	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10036553	TTAAAAGTAACTATT[C/G]GCCTGGTGCAGTGGC	2177
rs551629045	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10072721	TGCTATGCCAAAACA[A/G]TGTCAGATGACTTGA	2177
rs551656915	in-del	-/CTAA	0.000491116	0.0156626	intron-variant	FANCD2	GRCh38.p7	3:10060452	GATCAGTTAATCTTG[-/CTAA]CTAAGTGTTACATCT	2177
rs551709317	in-del	-/CC			intron-variant	FANCD2	GRCh38.p7	3:10069460	ACCCTAGTTAAGATG[-/CC]TCTCCCCCTCCCCCT	2177
rs551711253	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091797	GGACCCAAGACATAG[A/C]AGAATCAGCAACTAC	2177
rs551714254	in-del	-/AT	0.0361595	0.129508	intron-variant	FANCD2	GRCh38.p7	3:10054338	TTGAACAACCAGCAT[-/AT]ATATATATATATACG	2177
rs551756208	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10034910	TTTGGTGTAAGCTCT[C/G]TTTTCCTCAGAGTTT	2177
rs551760689	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10066176	CTTAGAATTCACTTC[A/G]CATTGCCCATGCTTT	2177
rs551763138	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026635	CCCACAGGTACCTTT[C/G]TGCGTCATTAAAATG	2177
rs551772768	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084961	AAAGGTGTCACTATG[A/G]TCTACACATGTATTG	2177
rs551831953	snp	C/G/T			intron-variant	FANCD2	GRCh38.p7	3:10038664	CAACTCACTGCAACC[C/G/T]CCGCCTTCTGGGTTC	2177
rs551852643	in-del	-/TT			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027318	GGATAGGAGGAACAC[-/TT]TTCAAGGAAGATGAC	2177
rs551853790	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100885	GACCAGCCTTGCCAA[C/T]GTGGAGAAACCCCGT	2177
rs551865809	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10054936	TTCAGTGAAAAATAA[A/C]TCTCACTTCTCAGTT	2177
rs551885235	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10055413	ATAAATGGAATCATA[C/T]GATATGTATCCTTTT	2177
rs551908965	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10055583	TTTGGGAGGCTGAGG[C/T]GGGCAGATCATGAGG	2177
rs551910933	snp	A/G	0.0103295	0.0711199	intron-variant	FANCD2	GRCh38.p7	3:10050165	GACCTAATCTACTCA[A/G]CATTGAGAGATAACT	2177
rs551919628	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10047361	CCAATAAAGCATTAT[A/G]CCCAGCTTAGTACTA	2177
rs551930456	snp	C/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10061200	TCTAGAAATCCCCAG[C/G]AAGCCGTTGTTTCCT	2177
rs551986199	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100412	GGAGTCTCCCTCTGT[C/T]GCCCAGGCTAGCATG	2177
rs552024889	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10075360	GGCTAATTTTTTGTA[C/T]ATTTTTTATAGAGAC	2177
rs552060725	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10030161	GAGTGCAGTGGCACA[A/G]TCTTGGCTCACTGCA	2177
rs552061421	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10046331	GTGCTGGGATTACAG[A/G]TGTGAGCCACTGTGC	2177
rs552126934	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10031336	GTGAAACCCCGTCTC[C/T]ACTAAAAATACAAAA	2177
rs552206789	snp	A/G	8.23621e-05	0.00641672	synonymous-codon	FANCD2	GRCh38.p7	3:10064424	CTCCTGTGTTGTTCC[A/G]GAAGGGTAGGTATTG	2177
rs552213192	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10058848	ATTCCATGTGAATTT[C/T]GGTATGGATCTTTCT	2177
rs552222077	snp	C/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10069625	CGCCGCCACGCCTGA[C/T]TGGTTTTCGTACTTT	2177
rs552270643	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10057658	ATGAGCTACTGCTCC[C/T]GGCCTCCATTAAGTT	2177
rs552306983	snp	G/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10051982	AGACATAACTTTTGG[G/T]AGAATATTGTTTTCA	2177
rs552308983	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10058184	TTCCGCACGAAGAGA[C/T]CGTGGAGATTAGGCC	2177
rs552361370	snp	C/T	0.0126979	0.078662	intron-variant	FANCD2	GRCh38.p7	3:10070831	TCGGTGACCTTACCC[C/T]CAACCCTGTGCTCTC	2177
rs552532007	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10055360	AATAATCACTAATCA[C/G]ATTCTGTCTATGGAT	2177
rs552573592	snp	C/T	0.00199481	0.0315187	utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101505	ATTCTCCTGCCTCAG[C/T]CTCCTGAGTAGCTGG	2177
rs552606107	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10060815	TGTGTATTTCCCCTC[A/G]CCTTGTTCCTTGAGG	2177
rs552637330	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10053337	GAACAGTGAGAACAC[A/T]TGGGCACAGGAAGGG	2177
rs552637787	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10102422	TGGTACAATTACAGG[C/T]GTGAGCCACCATGCC	2177
rs552670991	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10071388	AAGGAGATATCTGCA[C/T]TCCCATGTTTATTGC	2177
rs552693998	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10061359	CCGCCACCGGCTCAG[A/G]TAGTCATCACTCCCC	2177
rs552712189	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10049834	CCTGGGAAGCTGGAG[A/C]ATTCTTCAAAGAGGC	2177
rs552762156	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10067037	GCTGAATCTCCTATA[G/T]TTTGGGCCAGAGATT	2177
rs552778467	snp	C/G	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027474	CATGTGATTCAGGCA[C/G]TTCCCCCACCTCTGC	2177
rs552816589	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10054624	AAGTAGCTGGGACTA[C/T]AGGCGCCCGCCACCA	2177
rs552855591	snp	C/G	1.64844e-05	0.00287087	intron-variant	FANCD2	GRCh38.p7	3:10047898	GCTTCTTTTCTCTCT[C/G]TACTCTTCCCCACTC	2177
rs552885346	snp	C/T	6.58892e-05	0.00573936	synonymous-codon, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10081366	AGCTGCTGAGAATCA[C/T]GGTGTAGTTGATGGA	2177
rs552903954	snp	G/T	0.00199481	0.0315187	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097610	CTGTTGTTTTTTCAG[G/T]GTGCCCACATTTCAT	2177
rs552948635	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082052	AGCTATAGGCATTTA[C/T]ATCCAACTGCCTACG	2177
rs552950288	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10076020	ACAGGTGTGAGCCAC[C/T]GCGCCCAGCCATATC	2177
rs553031412	snp	A/G	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10079408	CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCTGCAG	2177
rs553094281	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10032093	CAGGTAATCAGCCTG[C/T]CTCGGCCTCCCAAAG	2177
rs553112950	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085134	CAGTTTGACAAAATT[A/C]TTCCTGTATTTTTGA	2177
rs553139063	snp	C/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10066440	GAGCTTATTTGATTA[C/T]CACATCTCTATTATG	2177
rs553180087	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026843	TGATAATGGTTATCC[A/G]TATTAACCGAAGCGG	2177
rs553221389	snp	C/T	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10055736	GGAATGGCGTGAACC[C/T]GGGATACGGAGCTTG	2177
rs553287456	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10045506	TGTAATATTCCAAAA[A/T]TTAAAATTACTCCAT	2177
rs553342175	snp	A/G	0.00159617	0.0282053	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088250	CGTGTTGAGCCTTAG[A/G]CAAATGAGTTTATGT	2177
rs553363014	snp	C/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10034222	CCAGCTACTTGGGGG[C/G]GCTGAGGCAGGAGAA	2177
rs553378875	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10067098	GTTCTATTACAGACT[A/G]AACTCAAAGATCTTG	2177
rs553398374	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10050448	CCTAACACGGTGAAA[A/C]CCCGTCTCTACTAAA	2177
rs553447170	snp	A/G	0.0023933	0.0345097	intron-variant	FANCD2	GRCh38.p7	3:10031226	GAGGGAAAGGAGGCC[A/G]GGCACGGTGGCTCAC	2177
rs553478426	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10067893	TGTAAATCAATGTGA[C/T]ACCTCCTATCAACAG	2177
rs553524388	snp	C/G	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10040760	TAGTTGTCTGCAAAG[C/G]TACCTCCAAAACATC	2177
rs553610585	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10036526	ACTTTGTAAAAATAG[A/G]TAGGATTACTGTTAA	2177
rs553621787	snp	A/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10058426	TTGCCGAATCCAAGG[A/T]CATGAAAGTTTTCTT	2177
rs553637428	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10045231	TGGACTGCACTGGCG[G/T]GATCTCGGCTCACTG	2177
rs553637932	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10040281	GACCTTGTGATCCGC[A/C]CTCCTCGGCCTCCCA	2177
rs553735210	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10071155	AAAAAAAGAAAAAAA[A/G]AAAAAGATGGCTTTT	2177
rs553745313	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10044002	TGCTCTAATAAACAT[C/T]AGCTGTCTGGGGAAG	2177
rs553786022	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10038189	TAGATATGAGGTTTC[A/G]CCATGTTGGCCAGGC	2177
rs553874354	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10076679	CTCAGCCTTCCAAGT[A/T]TCTAGGGCCACTGGC	2177
rs553875222	snp	A/G	6.69792e-05	0.00578663	intron-variant	FANCD2	GRCh38.p7	3:10049554	AATACTATAATTGGT[A/G]GGAGGTGGTGGGAAG	2177
rs553933973	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10043206	ACATCCCACTGTCAG[A/G]GTTAGAGCTTAATAC	2177
rs554003771	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10047545	TTAGCATTGAACCTT[A/G]TAGACCTACTTCAAA	2177
rs554026782	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025379	GATAAAATATGCAAA[C/T]GGAAAAATAATAGAT	2177
rs554033260	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094589	TTCTCCAGATCTGAC[A/G]GTGGTCTTCCTTTTA	2177
rs554040601	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10042890	TATGATGTTCTATGA[C/G]ATTGCATTGGCTATT	2177
rs554043344	snp	A/G	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10052582	GAGTGCAGTTGGCAC[A/G]ATCTCAGCTCATTGC	2177
rs554044201	snp	A/G	0.00676609	0.0577691	upstream-variant-2KB, nc-transcript-variant	FANCD2, CIDECP	GRCh38.p7	3:10026064	TACTTGTTCCTGGGT[A/G]AGCTTCTTGTCGCTC	2177
rs554047906	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095572	AGTCCTCTAGGTAAC[A/C]GGACTGTGATGTAAG	2177
rs554153645	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10044998	GTCTAATAACTCAGT[G/T]TTGGTGTCCTAAGAA	2177
rs554166629	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083047	GCCTGGGAAGCATGG[C/T]AAAACCCTGTCTCCA	2177
rs554180120	snp	A/G	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10040956	CCCAGCATGTTGGGC[A/G]GCTGAAGTGGGTGGG	2177
rs554208899	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10053904	CTAATGTGAACTTCA[C/T]GTGGGCTTGCTTTTG	2177
rs554229234	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10045053	AGTAAAATTTTTTTT[C/G]TTTTTTCTTGTTTGT	2177
rs554229799	snp	A/G	0.00119737	0.0244387	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083837	AGCTTGCAGTGAGCC[A/G]AGATCCCACCACTGC	2177
rs554229917	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10077642	TCCATAATCCCAATA[A/C]CTTGGGAGGCCAAGG	2177
rs554249904	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10048950	GTCATAATCCATGTT[C/T]GCTTGGAAACATGCA	2177
rs554312046	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10033133	TGGTACAGTCAGGCC[A/G]GGCGCGGTGGCTCAC	2177
rs554377839	snp	C/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10050931	CCTCTACTAAAAATA[C/G]AAAAATTACCTGGGC	2177
rs554382679	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096138	GGTGGTATGTCTTCT[A/G]GGCTTTGAATTCTTT	2177
rs554389554	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10060013	TCTCTACTAAAAATA[C/T]AAAATAAGCCGGGCA	2177
rs554503241	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093451	GAATCTATGCCAGTT[C/T]AGGGAAGGCAATGGA	2177
rs554536441	snp	G/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10065575	GCAGATCAATACATG[G/T]TGTATGTGGGGAGGA	2177
rs554548420	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093437	AGCCAGAGTTTCCAG[A/G]ATCTATGCCAGTTTA	2177
rs554549152	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10045410	CCTGACCTCATGATC[G/T]GCCCGCCTCGGCCTC	2177
rs554557253	snp	C/G	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086019	GGGTGTCTTTCAGTA[C/G]TTGTAAAGGAAATTA	2177
rs554564901	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10079451	CTGGGGACTACAGGC[A/G]CGCGCCACCACACCC	2177
rs554618594	snp	G/T	0.00159617	0.0282053	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086588	CTGGGCTCAAGTGAT[G/T]GTACTGCCTCAGCCT	2177
rs554672515	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10064126	AGAAGAGATTGACTT[C/T]GTTAATGATGATGGC	2177
rs554700295	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094057	AGTTCCCTGTCCATC[A/G]ACTGTATCTGTGGTA	2177
rs554722329	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098446	GACTTAGAGTCACCA[A/C]TACAGTCTAGCCTTT	2177
rs554742580	in-del	-/A			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098210	CTATTGTTTCTGCAT[-/A]AAAATTGAAGCTCAG	2177
rs554748265	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10069302	AAGATAGGAAAAAAA[A/G]TTATTCGGATTGAAA	2177
rs554794252	snp	A/G			intron-variant, downstream-variant-500B	FANCD2, FANCD2OS	GRCh38.p7	3:10099707	AGGTTGTGGTGAGCC[A/G]AGATCATGCTACTGC	2177
rs554903463	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10075656	TCTCTAGGTTTAAGA[G/T]AAATTGAAATAGCAT	2177
rs554984781	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100983	CTGAGGCAGGGGAAT[C/T]GCTTGAACCCGGGAG	2177
rs555004138	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10075106	TAGTACATAGAGCAT[C/T]ATGCTTGCTTTCAAA	2177
rs555205097	snp	A/G/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081853	ACCCCAGAAGGGTAC[A/G/T]TGGCCTTTAGAGAGA	2177
rs555206565	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10048739	TAACAATGTTAAAAC[A/G]CATTTGAATGGAACT	2177
rs555245317	snp	C/T	1.67329e-05	0.00289243	intron-variant	FANCD2	GRCh38.p7	3:10043804	TGTGTCATAATATTT[C/T]TGTGACTCTCTCCTG	2177
rs555260098	snp	A/G	0.0103295	0.0711199	intron-variant	FANCD2	GRCh38.p7	3:10056726	TAATCATTCTGATGA[A/G]TGCGAGTGGTATCTC	2177
rs555272534	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10077967	TGGGCCCAGGAGTTC[A/G]AGGCTGGAATAGCTA	2177
rs555279528	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10029908	CCAGCCTCAGTCTCC[C/T]GAGTAGCTGGGATTA	2177
rs555302395	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10038796	GTGTTGGCCAGGCTG[A/G]TCTTGAACTCCTGGC	2177
rs555328153	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10060770	GTCATTCCTGTCGGG[A/G]ACTTTATACATTTGA	2177
rs555348798	snp	C/T	4.94181e-05	0.00497057	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094295	CTTCTTCAGTATGGG[C/T]GTCTCTTTGTGGAAG	2177
rs555357392	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026761	AGATGGTATCGCACG[G/T]GTTAAAGGCGGGTGC	2177
rs555417460	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085030	GGAAGGGACAATATG[A/G]AAGGTAATCCAAAGA	2177
rs555435253	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10040238	AGACGGGGTTTCACC[A/G]TGTTAGCCAGGATGG	2177
rs555518997	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026324	AACTCTGCTGCAGCG[C/G]TGAGCCCAGCTTATT	2177
rs555529919	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10038114	TCCTGCCTCAGCCCC[C/T]CGAGTAGCTGGGATT	2177
rs555539811	snp	A/C	4.99239e-05	0.00499594	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095209	TTATAGGAAGATGTT[A/C]TGAGCTTACTGGAAA	2177
rs555611642	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082919	TATCAAAGAGACTTA[C/T]AGATGGCAAATAAAC	2177
rs555623633	snp	A/G	0.00199481	0.0315187	intron-variant	FANCD2	GRCh38.p7	3:10078992	ACACCTGTAATTCCA[A/G]CACGTTGGAAGGCCG	2177
rs555626508	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10035273	ACATTTGATGGAAGA[C/G]GTTTGTGGTGTATGC	2177
rs555687313	snp	C/T	0.00517822	0.0506191	intron-variant	FANCD2	GRCh38.p7	3:10036755	AGGATACACAATATA[C/T]TGGTAATGGTAGTTG	2177
rs555706467	in-del	-/A	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10063441	GCTCCATCTCAAAAG[-/A]AAAAAAAGAAAAAGC	2177
rs555746604	snp	C/T	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10034352	AAAAAAAAAGATTTG[C/T]CTCTGAAATTAGGTT	2177
rs555746907	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10059834	AAAAGTCCCCATTTC[A/G]CAGATGTAAAAATTA	2177
rs555758068	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10061323	CTGTCTTAGTAAATT[C/T]TCCCTCTAACCCCAC	2177
rs555779878	snp	A/T			missense	FANCD2	GRCh38.p7	3:10032964	CGGGAGAGAGTCAGA[A/T]TCAACTAGGTAATAT	2177
rs555841463	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10063478	AGAGAGAAAACAGAG[A/G]GCCTTGCATGTAAAG	2177
rs555870536	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10073224	GATTATTAATTACTT[A/G]AGTCACTTTTCTCTT	2177
rs555897211	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093916	GAGAGGAGTCATTTA[C/T]CTGATTGGGAAATTT	2177
rs555920199	snp	A/G	0	0	intron-variant	FANCD2	GRCh38.p7	3:10045445	AGTGCTGGGATTATA[A/G]GCGTGAGCCACCATG	2177
rs555943775	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10065076	CTTGTGTGAGCCAAC[A/G]GATATTCTGAGATTA	2177
rs555994063	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10050213	GGTGGATTGGAGACT[A/G]CTGAAATGGTCTAAG	2177
rs556032259	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093570	AATGGCTTCAGGGCA[G/T]TTGAGTTTAGGAGCA	2177
rs556032632	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10045148	ACACGCCCAATGTTT[C/T]CTCTTTTTTTGTTTT	2177
rs556054810	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091497	AAAAAAGAAAAAACA[C/T]ATACCGGCTGTAGCT	2177
rs556135413	snp	C/T	0.00478085	0.0486577	intron-variant	FANCD2	GRCh38.p7	3:10057315	TGATGCACTAAAGTA[C/T]TTAGTTTCAATAAAG	2177
rs556142760	snp	A/G	0.00199481	0.0315187	intron-variant	FANCD2	GRCh38.p7	3:10060198	CAGTTAGTAAACGGT[A/G]AACGCCTTTATAGTC	2177
rs556198230	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10069802	GCAGTAGCGTGATCT[C/T]GGCTCGCTACAACCT	2177
rs556213768	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10052782	ACATGAAAAAGTGCT[C/T]ATCATCACTGGCCAT	2177
rs556247589	snp	C/T	0.0103295	0.0711199	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092621	TCTCACCCACTCCAT[C/T]GTGGTTTTGCTCAGC	2177
rs556259383	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10046955	GGAATAGGACCAGCC[C/T]GTAGAAACTAGTAGA	2177
rs556291642	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10024699	ATTAAAAATTTCTTG[C/T]GGAATTTGCAAACTT	2177
rs556294044	snp	A/G	0.00318978	0.0398085	intron-variant	FANCD2	GRCh38.p7	3:10047454	AGTCTGGGTCCATTA[A/G]TGTCTATGTACATTG	2177
rs556330979	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10075567	AGAATGATGTTTATA[C/T]AGAAGTTGGGAGTAG	2177
rs556414911	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100430	CCAGGCTAGCATGCA[A/G]TGGTGCAGTCTCAGC	2177
rs556493386	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10080322	CACTGCAACCTCCAC[C/T]TCCGGGATTCAAGTA	2177
rs556494105	snp	C/T	0.00199481	0.0315187	intron-variant	FANCD2	GRCh38.p7	3:10070973	CCTAATCTCAAGTAC[C/T]CAGGGACACAAACAC	2177
rs556513844	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10050472	TACTAAAAATACAAA[A/C]ATTAGCCGGGCATCG	2177
rs556548817	snp	A/G	0.000494063	0.0157095	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088921	CTCTCCTAAAGATGC[A/G]TCTTCCTCCACATTC	2177
rs556589395	snp	G/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10055431	TATGTATCCTTTTGC[G/T]TCTCGCTTATTTCAC	2177
rs556629621	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10053414	GATAGCATTGGGAGA[C/T]ACACCTAATGCTAGA	2177
rs556678170	snp	A/T	0.00438332	0.0466095	intron-variant	FANCD2	GRCh38.p7	3:10055822	GTCTCAAAAAAAAAA[A/T]AATAATAAATAAATA	2177
rs556734130	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10043983	CTTCTCTCTCTTCCC[C/T]AGTTGCTCTAATAAA	2177
rs556744020	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101693	CAGCCATATTTTGTT[C/T]TTAAAGTGGGGTCTT	2177
rs556774539	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027944	TTCTTTAGGCCGGGC[A/G]GCTCACACCTGTAAT	2177
rs556888101	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10067733	AACCTGGGAGGCGGA[A/G]GTTGCAGTGAGCCAA	2177
rs556920708	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097195	ACATGACCGCAGGAC[C/T]GAGGCGAAATTGAAA	2177
rs556950880	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091996	TCCCTATGAGGTGTT[C/T]TAATGTTACCACAAC	2177
rs556999159	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10068591	ATCTACAGATTCAAG[G/T]CAATCCCTATTAAAA	2177
rs557004916	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10078475	TTCTCCTGCCTCAGC[C/T]TCCCGAGTAGCTGGG	2177
rs557070078	snp	G/T	0.0023933	0.0345097	intron-variant	FANCD2	GRCh38.p7	3:10053834	CATGAAACTGTTCAG[G/T]TTCTGAGTGCAGTGG	2177
rs557090101	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10063306	GCTGGACATGGTGGC[A/G]GGCGCCTGTAGTCCC	2177
rs557133482	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10061494	ATTGTTTATTAGCTG[A/T]ATTACCTTGGGTAAG	2177
rs557197270	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10050900	GAATCAGCCTGACCA[A/G]CATGGAGAAAGCCCT	2177
rs557270697	snp	A/G	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10067099	TTCTATTACAGACTA[A/G]ACTCAAAGATCTTGC	2177
rs557372533	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10045883	GGGATTACAGGCGTG[A/C]GCCACCGTGCCTGGC	2177
rs557416506	snp	A/G	0.00358779	0.0422022	intron-variant	FANCD2	GRCh38.p7	3:10071187	TCCAAAGGACAGGCA[A/G]TAACAGATGCTGGTG	2177
rs557418746	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10077332	GAGGCTGAGACAGGC[A/G]TTATCACCTGAGGTC	2177
rs557425572	snp	C/T	0.00993419	0.0697739	intron-variant	FANCD2	GRCh38.p7	3:10040257	TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTTG	2177
rs557478071	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10071785	GTATTTTTGAGATGG[A/T]GTCTCGCTCTGTCAC	2177
rs557503450	in-del	-/GTAT	0.1652	0.235179	intron-variant	FANCD2	GRCh38.p7	3:10054397	TATATATGTATATAC[-/GTAT]ATGTATATACGTATA	2177
rs557508130	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10029078	AAAAAATATTATGAT[C/T]TAGACACATGCTATG	2177
rs557555363	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10076762	ACGGAGTCTTGCTCT[A/G]TCCGTCAGTCTGGAG	2177
rs557615082	snp	A/G	0.0111196	0.0737302	intron-variant	FANCD2	GRCh38.p7	3:10065319	GTTCCCTATGTATGT[A/G]GAGTAATATCTCCCT	2177
rs557618215	snp	A/G	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10034305	ACTCCAGCCTAGGCA[A/G]CAGAACAAAACTCCA	2177
rs557736250	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10047657	AAATTGAGCAGATAG[A/G]AATGTTCTATTAGGC	2177
rs557755559	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10032136	AGGCGTGAGCCACTG[C/T]GCTGGGTCGGAAATA	2177
rs557772775	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10042897	TTCTATGACATTGCA[C/T]TGGCTATTCTCATAA	2177
rs557888759	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10034249	AGAATCATTTGAACC[C/T]AGGAGGCGGAAGTTC	2177
rs557890477	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090927	TCTTTTCCTTGGCTA[C/T]TGCCCAGTTTGCCTC	2177
rs557893251	snp	G/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10039560	AAGAGTAGATATCAT[G/T]TATTAAATAAATTAA	2177
rs557900765	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096999	ATTTTAAAGCTGGGC[G/T]TCCGGGGGAGACATC	2177
rs557901937	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10038021	TTTGAGACGGAATCT[C/T]ACTCTGTTGCCCAGG	2177
rs557925061	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10043287	TTTTCAAATTACATA[C/T]ATGTATGTGAGTATG	2177
rs558022247	snp	A/C/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090033	CAGGACTCAAACTCA[A/C/G]ATCTTCTCACTGTTA	2177
rs558053455	snp	A/C	0.00438332	0.0466095	intron-variant	FANCD2	GRCh38.p7	3:10062631	AAGTGCTTCTTTTGT[A/C]AAAGAAGTTTTCCTG	2177
rs558120693	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10038949	TTAAAAATACTTGTC[A/G]TATTCAGTTTTTAAG	2177
rs558158498	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10035098	ATGTATTTAACCAAT[C/T]TTATTGAGAAAAGAT	2177
rs558158620	snp	C/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10042204	CCTGGCCCACAGGTC[C/T]GTTTTTAAGCAGTAA	2177
rs558205181	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10078511	AGGTGCCTGCCACCA[C/T]GCCTGGCTAATTTTT	2177
rs558207173	snp	C/T	0	0	intron-variant	FANCD2	GRCh38.p7	3:10072547	ACCTCCCAAAGTGCT[C/T]GGGGTTACAGGCGCG	2177
rs558209870	snp	A/G			upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10024923	AACAAGTGTTTTTTC[A/G]TTTGTTTTTCTGGAG	2177
rs558229197	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083967	AGCCTGTGGTTTTAC[A/G]TAGTATATTCTAAAC	2177
rs558301802	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10099505	TGGCTCACACCTGTA[A/G]TCCCAGCACTTTGGG	2177
rs558337011	snp	A/G	0.00279162	0.0372561	intron-variant	FANCD2	GRCh38.p7	3:10051346	AGATCCCGCCACTGC[A/G]CTCCAGCCTGGGCGA	2177
rs558359799	snp	C/G	0.0103295	0.0711199	intron-variant	FANCD2	GRCh38.p7	3:10049069	AACCTCAACCTAAAG[C/G]GTAAAATTTAACCCA	2177
rs558362135	snp	A/G	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10054419	TATATACGTATATAC[A/G]TATATACATGTATAT	2177
rs558363562	snp	C/T	0.00159617	0.0282053	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086641	CGCATGCTGACACAC[C/T]CTACTAATTTTTATA	2177
rs558364451	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090620	TGCGCCACCACACCC[A/G]GCTAATTTTTATATT	2177
rs558373331	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10046309	CTGCCCGCCTTGGCC[A/T]CCCAAAGTGCTGGGA	2177
rs558382840	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10060103	ACCTGGGAGGCAGAG[A/G]TTGCAGTGAGCCGAG	2177
rs558502169	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093480	GATGCATTTTCCCAC[A/C]CTAGTTGGATGATTG	2177
rs558528031	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10054086	GTGTGGTGGCACACA[C/G]CTGTAATCCTAGCTA	2177
rs558580898	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10057996	TAGTAGCTTTTTTGA[A/G]TTAAGCTATCAAGTT	2177
rs558633597	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10030218	TCTCCTGGCTCAGCC[A/G]CCCAAGTAGCTGGGA	2177
rs558667715	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10058503	GATCCACTTTGTGTT[A/T]ATTTTTGTATATAGC	2177
rs558696722	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10049320	GGGTGAATCCCTTTA[C/G]AATGGCCATCCATAT	2177
rs558698348	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10051041	CAGTGAGCTGAGATC[A/G]TGCCATCACACTCCA	2177
rs558765131	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10057174	TGCCCATTTTTAAAT[C/T]AGGTTTTTGTCGTTT	2177
rs558861412	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10062518	AAGTGCTGGGAGTAC[A/G]GGCGTGAGCCACCTC	2177
rs558894791	snp	G/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10064164	TGTCTGAGAGCCCTA[G/T]TCTGTGCTGGGCCTT	2177
rs558949899	in-del	-/T	0.00159617	0.0282053	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090847	TTCTGAGATTCAGGA[-/T]TTTTTTTTCAAAGAG	2177
rs558964282	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094705	CTCTCAGAAATGATT[A/T]TAAAAAAAAAAAAGC	2177
rs558997066	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10024602	AAATAAATAGATGTC[C/T]TTCAGTTACAAATTA	2177
rs559032815	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10069732	GCCTCCCGAGGTGCC[A/G]GGATTGCAGACGGAG	2177
rs559055045	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090831	TTTGTTTTGTTTTGA[C/G]TTTCTGAGATTCAGG	2177
rs559093929	snp	C/T			intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10098951	CCATTCCCTCCATAA[C/T]AGCTTCTGTGCTTAT	2177
rs559101209	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100994	GAATCGCTTGAACCC[A/G]GGAGGCAGAGGTTGC	2177
rs559114192	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10070176	AGAAGTGAGGAGACC[C/T]TCCGCCCGGCAACCG	2177
rs559140072	snp	A/G	5.23857e-05	0.00511763	intron-variant	FANCD2	GRCh38.p7	3:10060260	TTGCTGTGCCATTCC[A/G]GCATTTTCATCTTTC	2177
rs559242494	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026349	CTTATTGCCTTCAGC[G/T]GGGCTGCCCGGCCTT	2177
rs559251352	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10059670	ATCCGGGCGTGGTTG[G/T]TGGCGGGCACCTGTA	2177
rs559255310	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10074379	CTGTCTTGGGAATAT[A/T]TAGGGACTTGGGCTA	2177
rs559267404	snp	A/G	1.65222e-05	0.00287417	synonymous-codon	FANCD2	GRCh38.p7	3:10065889	ATTCCTAACTGACCT[A/G]GAGCCTGGAGAGAAG	2177
rs559276264	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10075509	ATTGATGCCAAATAC[A/G]GCATTAATGGTCTGA	2177
rs559303952	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098137	ATATATGAAATATAT[A/G]AAACAGCACCACAGA	2177
rs559365923	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098526	ACTTATTGTATCAGG[G/T]CCACAGACATCTCAG	2177
rs559412964	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10031449	GGAGCTTGCAGTGAG[C/T]CAAGATCGCGCCACT	2177
rs559440635	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10049209	CACTGGCATATTCCT[A/G]AATCTCCTGAAGCCA	2177
rs559622868	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025926	AGAGGTAACGGGTAA[A/G]GTCACCTTGCCAGTG	2177
rs559702915	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10102379	TGAACTCCTGACCTC[A/G]TGATCTACCCGCCTC	2177
rs559744107	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091770	AACAAAAAACAGCTT[A/G]GGAGAAAACTTGGAC	2177
rs559831106	snp	C/T	0.0232847	0.105357	intron-variant	FANCD2	GRCh38.p7	3:10041837	GAATCACATTTGATA[C/T]CTCTCTTTTTTTTTT	2177
rs559874184	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10080988	TTAACAACTCATTTC[C/T]CCCATCTGCTCCTAC	2177
rs559876484	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100820	CACGCCTGTAATCCT[A/T]GCACTTTGGGAGGCT	2177
rs559888047	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10078995	CCTGTAATTCCAGCA[C/T]GTTGGAAGGCCGAGG	2177
rs559914149	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10061836	CTTATTGGCAGTTGT[C/T]ACAAAATATTACAAA	2177
rs559922736	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027235	CAAAGAGCCCCAGTC[C/T]AGTGTGAGGTAAGGG	2177
rs559937725	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094443	TGACTCCTGGGTGGG[A/G]CTGGGAGTGTTCTAC	2177
rs560024225	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10033054	TCTAAATAGAGAGGC[A/G]ATGAAGATTAGAAAT	2177
rs560034787	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10037528	GATAATAACTGTGAA[G/T]GAAAATGAAATAATA	2177
rs560091303	snp	C/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10039115	CGTAAGCATGTATCT[C/G]CTGCATCTTGGGTAT	2177
rs560108670	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10069541	GTACTGCTGCCATCT[C/T]GGCTCACTGCAACCT	2177
rs560175963	snp	A/G	0.0154538	0.0865337	intron-variant	FANCD2	GRCh38.p7	3:10069879	AGCCTCTGCCCGGCC[A/G]CCACCCCGTCTGGGA	2177
rs560184910	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10042998	AGAGACTGGACTGTG[C/G]CTACCCACTATGAAT	2177
rs560195195	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10064914	AACCTGTTAGTGTTT[G/T]GAATGTTCATGGGGA	2177
rs560221032	snp	A/C	1.69697e-05	0.00291283	intron-variant	FANCD2	GRCh38.p7	3:10043457	GGTACGTAGAAGAGT[A/C]ATTTTTTTCCTCTCT	2177
rs560222896	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10036788	TCCAAAGAGGGTAGC[C/T]AGTTGGTTGGAATCA	2177
rs560378773	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10076453	TATTATTTTACTATT[C/G]TGAATATTTATTTTG	2177
rs560384282	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10042352	TCTGTTTCACATTTA[C/T]TGCCCGTCTATTTTT	2177
rs560453253	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10077062	AGTGAGACCTGTCTC[C/T]ACAAAAAGTTAAAAA	2177
rs560458083	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10046342	ACAGATGTGAGCCAC[C/T]GTGCCTGGCCTGCTC	2177
rs560460213	in-del	-/A	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10068352	ACAACTAAGAATCTG[-/A]AAAAAATCAAGAAAG	2177
rs560556160	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10071372	AGGAAATCAGTATAC[C/T]AAGGAGATATCTGCA	2177
rs560563367	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082428	GTGATCTTCCTAACA[G/T]AAACCCAGTTTGATC	2177
rs560568689	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10031332	CATGGTGAAACCCCG[C/T]CTCTACTAAAAATAC	2177
rs560600678	snp	A/G	0.000856235	0.0206733	synonymous-codon	FANCD2	GRCh38.p7	3:10065406	CAGATTGGTGTCTCC[A/G]CTGTGCCTGGCTCCG	2177
rs560661123	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10045715	CAAGCGATTCTCCTG[C/T]CTCAGCTTCCCAAGT	2177
rs560674980	snp	C/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10079167	AAGACTTGATTGAAC[C/G]CAGGAGGCAGACGCT	2177
rs560686087	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10058582	TCCAGTTTTTCCAGT[A/G]CCAATTTGTTGAGAA	2177
rs560725116	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10058839	TCCCTTGAAATTCCA[C/T]GTGAATTTTGGTATG	2177
rs560753708	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10033965	GCCTCCCAAAGTGCT[A/G]GGATTACAGGCATGA	2177
rs560851073	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094902	AGCCCTGAAAGAGAA[A/G]GGGAAGGTGGTATTT	2177
rs560885919	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10053077	TAAAGACACATGCAC[A/G]CATATGTTTATTGCG	2177
rs560907485	snp	A/G	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10050363	GGTGCGGTGGCTCAT[A/G]CTTGTAATCCCAGCA	2177
rs561035044	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10078702	GGCGTGGTGGCTCAC[A/G]CCTGTAATGCCAGCA	2177
rs561037559	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091622	TTACCTCATGCCAGT[C/T]AGCAGGAGGCAAACT	2177
rs561038450	snp	G/T	0.00199481	0.0315187	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097950	GGTCCCTGACTTCCC[G/T]CAACAATCTCTAATT	2177
rs561050018	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10039984	TGAGTAGGGTATGGG[A/C]TTTGACTTAAAAAAA	2177
rs561072896	in-del	-/T	0.339203	0.233544	intron-variant	FANCD2	GRCh38.p7	3:10072281	ATATATACCTTTCCC[-/T]TTTTTTTTTTTTTTT	2177
rs561073008	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10055540	ATTCTTGGCCGGGCA[C/G]GGTGACTCACGCCTG	2177
rs561183655	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10056886	TTGAGATGGGGTCTC[A/T]CTCTGTCACACACAT	2177
rs561195125	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10054807	ATATTTTTTATCTTT[C/T]TTTCCCCCCCTTTCT	2177
rs561205028	snp	C/T	1.65228e-05	0.00287422	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092301	AATAACTGCAGAAAC[C/T]AAGTGTCCTGGCTTC	2177
rs561218090	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101336	TAGAGTTTGAAATCC[A/G]CTGTTTGCCTTTCTT	2177
rs561269549	snp	A/C	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10051145	CAGCACTTTGGGAGG[A/C]CGAGGTGGGCGGATC	2177
rs561289234	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10062316	CAAGATCTCGGCTCA[C/T]TGCAACCTCCACCTC	2177
rs561290805	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10068724	TGAAACTGGAGGAAT[C/T]GCATTACCTGACTTC	2177
rs561308300	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093628	CAGGCAAAAGGGAGG[A/G]AGGAGGAGTAGATGA	2177
rs561313038	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10089346	CCACACAACTGCCTT[G/T]CTCCTCCTCATCTAA	2177
rs561320448	snp	C/T	0.0611083	0.163768	intron-variant	FANCD2	GRCh38.p7	3:10051602	AATGTCGAGAAGCAT[C/T]AAGGAGGAGAGAATA	2177
rs561370225	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10099104	ATTCATATCTGAAAC[C/T]ATTTTAGAAGGGAGA	2177
rs561373993	snp	C/G	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090101	TCATAAAGTTAATTC[C/G]ATTGTTTGACAGGCA	2177
rs561395054	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10044483	GACCAGCCTGGCCAA[C/T]GTAGCGAAACCCCGT	2177
rs561448636	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095912	TTTGAGACGGAGTCT[C/T]GCTTTGTAGCCCAGG	2177
rs561491242	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096541	CATCAGATGGCATGT[A/G]AGGAAGGTCACCTAA	2177
rs561548686	snp	G/T	4.94181e-05	0.00497057	missense	FANCD2	GRCh38.p7	3:10065396	TTCTCCTTCTCAGAT[G/T]GGTGTCTCCGCTGTG	2177
rs561606588	snp	A/C/G	0	0	intron-variant	FANCD2	GRCh38.p7	3:10074518	CTCTTTGTTGCTGTG[A/C/G]CTTCCCCATAGGAGT	2177
rs561688166	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10065004	TTTGGAGAGGTTAGG[A/G]AGAATGGGGCAGATT	2177
rs561689093	snp	C/T	0.0119091	0.0762411	intron-variant	FANCD2	GRCh38.p7	3:10054388	ATATACATATATATA[C/T]GTATATACGTATATG	2177
rs561689113	snp	A/G/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10067614	ACCAGCCTGGCCAAC[A/G/T]TGGTGAAACCCTGTT	2177
rs561689920	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10071295	GGAGTTTCCTCAAAA[A/C]ACTAAAAATAGAATC	2177
rs561719635	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101370	GGTAGGATCCTTTTT[C/T]GTTCCTCTTTTTTTT	2177
rs561781834	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10059625	GGCTAACATGGTGAA[A/G]CCCCGTCTCTACTAA	2177
rs561789663	in-del	-/TCT	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10079917	CATTTTTCTTCTTCG[-/TCT]TCTTTTTTTTTTTTG	2177
rs561790421	snp	A/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027566	TCTTCTCCTACCCCT[A/T]CTACTGGCTAACTGC	2177
rs561823017	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025108	ACAGGCACACACCAC[C/T]GCACCTGGCTAATGT	2177
rs561823138	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10031329	TAACATGGTGAAACC[C/T]CGTCTCTACTAAAAA	2177
rs561899502	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10041034	AGCCGTCTTTCAAAA[A/G]CATACAAAAATTAGG	2177
rs561901522	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083996	ACTTGTTTCCCATGC[C/T]TTTGTGTGTGTGTGA	2177
rs561925804	in-del	-/TATGTC			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088261	TTAGGCAAATGAGTT[-/TATGTC]TGGCAAAAGGGCCAG	2177
rs561956900	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10102132	GATTGACTTGATCTT[A/G]ATCTTCTTTCCTTTT	2177
rs561959845	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10037846	AGTTTTTGCAATAAG[C/T]AGTTCAGTATTTTGT	2177
rs562020109	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10072616	TGTTTTAGTTTTTTT[C/T]TGTTTGTTAGTTATA	2177
rs562117400	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085226	ACCTATGGCCCAGGC[A/G]TGGTGGCTCACCCCT	2177
rs562133719	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10061085	CCCTCCTGCGCCCAA[C/T]TTAATCACCAGACAC	2177
rs562135363	snp	C/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10029942	GCGCCAGCCACCATG[C/G]CCGGCTGATTTTTTT	2177
rs562159676	snp	A/G	0.00119737	0.0244387	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097399	GAGACAGGTACACCC[A/G]GGGGGGCCCAGTTCA	2177
rs562247333	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10029420	GTGGAAGGATCACTT[C/G]AGCTCAGGAGGTCGA	2177
rs562286067	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10072053	GCATGAGCCAGAGAG[C/T]CCAGCCAAGATCTAG	2177
rs562303208	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10038493	TGATAATTGAGCCAA[C/T]ATTTCTTTATTTATA	2177
rs562346789	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10063657	GACGGGTCAGAACAT[G/T]CAGGAAAACTTCAAG	2177
rs562381605	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100346	ACAGAACAGAATTTT[G/T]TACTGGATTCCTGTT	2177
rs562500382	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10079616	TAGGCGTGAGCACTG[C/T]GCCCAGCCTACGAAA	2177
rs562568236	snp	A/G	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10041865	TTTTTTTTCCCCTCA[A/G]TGAGTTTCAGATGCT	2177
rs562602283	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10032749	GACACATCAGTTTTC[C/T]TCTCATGATTATTAT	2177
rs562606778	snp	C/T	1.64784e-05	0.00287035	intron-variant	FANCD2	GRCh38.p7	3:10035276	TTTGATGGAAGAGGT[C/T]TGTGGTGTATGCTCA	2177
rs562612052	snp	C/T	0.00795532	0.062565	intron-variant	FANCD2	GRCh38.p7	3:10069495	CCTCCCCCTCTCCCG[C/T]CTCCCTCTGATGCCG	2177
rs562627987	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086174	TTTCAAGTAATAATG[A/G]TGAAAACATTGACCA	2177
rs562696555	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10075879	GGGACTACAGGTGCC[C/T]GCCACCATGCCTGGC	2177
rs562716514	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10080366	AGCCTCCTGAGTAGC[C/T]AGGACCACAGGCATG	2177
rs562745018	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10045742	AAGTAGGTGGGATTA[C/T]AGGTGTGTGCTACTT	2177
rs562765682	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10053561	AAATAGAATAAAATT[A/T]AAAAAAATTTTTTTG	2177
rs562780792	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10046144	CTGTAAGCTCTGCCT[C/T]CCGGGTTCACGCCAT	2177
rs562846815	in-del	-/AA	0.00478085	0.0486577	intron-variant	FANCD2	GRCh38.p7	3:10067949	TTTAAATTGATGCTT[-/AA]AAAAATTTTATAAAA	2177
rs562856650	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081866	ACATGGCCTTTAGAG[A/T]GATAACGGAAGGAAG	2177
rs562880198	in-del	-/T	0.00676609	0.0577691	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093101	TTGCTCGTCTCTTCC[-/T]TTTCTTGAACTTCAG	2177
rs562892293	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10051743	GAGATTTTTAAAAAT[C/T]AATTAAAAGTTTACA	2177
rs562899539	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10042936	TTCAAAATGTCCAAC[A/G]TTTAAATTTTTTTCT	2177
rs562901232	snp	A/G	0.00438332	0.0466095	intron-variant	FANCD2	GRCh38.p7	3:10075285	GCCTCCCGGGTTCAC[A/G]CCATTCTGCTGCCTC	2177
rs562959478	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088277	ATGTCTGGCAAAAGG[A/G]CCAGTGGATCAGGAA	2177
rs562980879	in-del	-/A			intron-variant	FANCD2	GRCh38.p7	3:10053623	CTTGAAATTTGCTAG[-/A]AAAAAAAAAAACAAG	2177
rs562996800	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10049907	AAGTATGGGAAGTGC[A/G]TTCTAGGCAGAGAAG	2177
rs563068808	snp	C/G	1.64749e-05	0.00287005	missense	FANCD2	GRCh38.p7	3:10041643	TACTGATAGAGAATA[C/G]TTCACTCACTGTCCC	2177
rs563114815	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10045269	CGCCTCCTGGGTTCA[C/T]GCCATTCTCCCGCTT	2177
rs563131146	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10048215	AAGGAAGAGACTTGA[C/T]TGGTGGCTCTAACTC	2177
rs563131262	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10032043	AGAGATGGGGTTTCA[C/T]CACGTTAGCCAGGCT	2177
rs563137494	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10074866	AGGTTTGTAATAATG[C/T]GTCAGACATTATAAA	2177
rs563144914	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10043253	ACTATTATGACATTT[A/G]CATCTAGTATTATAT	2177
rs563151437	snp	A/C	0.00398564	0.0444627	intron-variant	FANCD2	GRCh38.p7	3:10078647	GCATGAGCCACCGCG[A/C]CCGGCCTCATCTTGC	2177
rs563161351	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10064222	CTTTTCTACTTCACA[A/T]TAGTGAGATATTTAT	2177
rs563178975	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093737	GAATAGCCTGTATTA[A/G]CCCTAGATTTGATGG	2177
rs563243909	snp	A/G	0.0023933	0.0345097	intron-variant	FANCD2	GRCh38.p7	3:10058075	GATGTACTTCTTGGG[A/G]TTCTCCAAATACTCC	2177
rs563273285	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10039193	AATGTTAATGGAATG[A/G]CTAAAATATTTTGTG	2177
rs563283766	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10076362	TTAGGAAACGCATCT[G/T]GGATCCACAACTAGA	2177
rs563291828	snp	C/T	0.0023933	0.0345097	intron-variant	FANCD2	GRCh38.p7	3:10054350	GCATATATATATATA[C/T]ACGTATATATATATA	2177
rs563307388	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10099027	ACTCCTGAGTATCTC[A/G]AGTTGTGGCATTTGT	2177
rs563366126	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091595	GATCCACAGTATCTC[A/G]AACAGGCTGGCTTAC	2177
rs563368606	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092944	TGATCCACCAGCCTC[A/C]GCCTCCCAAAATGCT	2177
rs563384313	snp	A/G	0.00159617	0.0282053	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084205	CACCATCTTGGCCAG[A/G]CTGGTCTTGAACTCC	2177
rs563423275	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10066495	TCATTTTACACATAC[A/G]AATTTCAATAGGGAG	2177
rs563437411	snp	A/C	0.00199481	0.0315187	intron-variant	FANCD2	GRCh38.p7	3:10044884	CATTGTATAAATATA[A/C]TTTGTATTCTTACTT	2177
rs563440424	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097336	TAATAAGCCTGGGAG[C/T]GCTATAGGAGACTGG	2177
rs563505860	snp	C/G	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091009	GCAGCCTGCTAACCA[C/G]AACGGAGCTAGACAA	2177
rs563540093	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10067959	TGCTTAAAAAAATTT[C/T]ATAAAATTCAACATC	2177
rs563561289	snp	A/G	3.34191e-05	0.0040876	intron-variant	FANCD2	GRCh38.p7	3:10060410	GGCAGACAGGTACAC[A/G]TGGAGATTCTGACTT	2177
rs563678789	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10067394	AGCTTTCCCTGATAC[C/T]AAAACCAGACAAAGA	2177
rs563678852	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10073981	GATGGAGTCTCACTC[C/T]GTCACCCAGGCTGGA	2177
rs563707444	snp	A/C	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094993	GGTCTTATAACTCTC[A/C]GATTGATACAAGGGA	2177
rs563726660	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085626	CCATGTGTTGACCTC[A/G]TTATTCGCCCGCCTC	2177
rs563768666	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095770	TTTGTCTGAATGAAC[A/G]CAGAACCCTAGAGTT	2177
rs563842075	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101335	TTAGAGTTTGAAATC[C/T]GCTGTTTGCCTTTCT	2177
rs563866026	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027677	TTGGGAGTCCGAGGC[A/G]GGCGGATTATGAGGT	2177
rs563930793	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10061911	CACTCATAGGTGGTA[A/G]TTGAACAATGAGAAC	2177
rs563974522	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10033174	CCAGCACTTTGGGAG[A/G]CTCGAGGCAGGCGGA	2177
rs564067452	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10051810	AAAGGTAGTATAGCT[A/G]TTATTATCACCATGT	2177
rs564084457	snp	C/T	0.00279162	0.0372561	intron-variant	FANCD2	GRCh38.p7	3:10053250	GGATGAAATTGGAAA[C/T]CATCATTCTCAGTAA	2177
rs564084819	snp	C/T	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10059577	GGAGGCCAAGACAGG[C/T]GGATCACGAGGTCAG	2177
rs564087277	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10069994	GCGTCTCTGCCCGGC[C/T]GCCATCCCATCTAGG	2177
rs564150983	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10064512	ACAAACTTCAGAATA[C/T]CCTTCACCTCAGCCA	2177
rs564195102	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10064976	AAAAAAGTTTCTCTC[A/G]AGACAAATGGTATTT	2177
rs564208578	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10037618	CATGGCCCTTTTGCA[A/G]GGGTGATACCCAAAT	2177
rs564246252	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10031338	GAAACCCCGTCTCTA[C/T]TAAAAATACAAAAAA	2177
rs564246338	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10038235	GACCTCAAGTGATCT[G/T]CTTGCCTCAGCCCCA	2177
rs564330583	snp	C/T	0.0174175	0.0916809	intron-variant	FANCD2	GRCh38.p7	3:10070356	CCCCGCCAGGCCAGC[C/T]GCCCCGTCCGGGAGG	2177
rs564342097	in-del	-/A	0.00119737	0.0244387	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10089131	CCCTACTAAAAATAC[-/A]AAAATTAGCCGGGCG	2177
rs564373560	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10042429	AATCTAAAATTTTGT[G/T]TTTCCCTAAATTATA	2177
rs564387320	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10044134	AGCACATCAAGGTGC[A/T]GTCAAAGAAGCCAGG	2177
rs564450796	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10031371	AGCCGGGCGTGGTGG[C/T]GTGCACCTGTAGTCC	2177
rs564477216	snp	C/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084695	CACCTAATAGGCCCT[C/G]AGAATACATTTGTTG	2177
rs564528633	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10034611	TAAGGACACTGGTAT[A/G]AAGTTGAGTGGGCTA	2177
rs564536759	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096224	CCGTTGGCCCATACT[A/G]GCAGGGCTTGTGTTC	2177
rs564540459	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083224	AGAACCAGACCCCAT[C/T]TCAAAAAAAAAAAAA	2177
rs564547673	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10071394	ATATCTGCACTCCCA[A/T]GTTTATTGCAGCACT	2177
rs564577177	snp	A/G/T	0.00023061	0.0107357	synonymous-codon	FANCD2	GRCh38.p7	3:10047949	TTCATCCATTCTGTC[A/G/T]CTGGCTCAGAGTTTG	2177
rs564643032	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10041039	TCTTTCAAAAACATA[C/G]AAAAATTAGGTGGGC	2177
rs564659254	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10035976	CTTTGTATTCCAATA[A/G]CATATTCTAAAAATG	2177
rs564685142	snp	C/T	0.0494327	0.149241	intron-variant	FANCD2	GRCh38.p7	3:10077132	CAGCTACCTGGGCGG[C/T]TGAGGTGGGACCATC	2177
rs564837602	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10048525	GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG	2177
rs564870333	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10069330	AAAAATGGGTAAAAG[A/G]TCTGAATAGACATTT	2177
rs564888544	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10080663	GTGGTCTCAGATACT[C/T]AGGAGGCTGAGGTGA	2177
rs564912443	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10045730	TCTCAGCTTCCCAAG[C/T]AGGTGGGATTACAGG	2177
rs564959157	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10046116	TGGAGTGCAGTGGCG[C/T]GATCTCGGCTCACTG	2177
rs564969772	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10074038	GCAACCTCCACCTCC[C/T]GGGTTCAAGCGATTC	2177
rs564971759	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10079555	ATGATCCGCCCACCT[C/T]GGCCTCCCAATCCGC	2177
rs564972753	snp	C/T	0.00199481	0.0315187	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081018	CCTGGTGACACAGGT[C/T]TGACTTGACTCCATT	2177
rs564989347	snp	C/G	0.0611083	0.163768	intron-variant	FANCD2	GRCh38.p7	3:10051605	GTCGAGAAGCATCAA[C/G]GAGGAGAGAATAAAA	2177
rs565130846	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10055929	TGTCGCCCAGGCTTG[A/G]GTGCAATGGCACAAT	2177
rs565152570	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10057537	GCCCAGTTAATTTTT[A/G]TATTTTTAGTAGAGA	2177
rs565339697	snp	A/G			synonymous-codon	FANCD2	GRCh38.p7	3:10043502	CTCAGGAAATCAAGA[A/G]AGCAGCGGTCAGAGC	2177
rs565351425	in-del	-/TT			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092709	TTTTTTTTTTTTTTT[-/TT]GAGGCAGGGTCTCAC	2177
rs565369707	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095686	TCATCTATGTCTTAT[A/G]AGAACATCTTAGCAT	2177
rs565387152	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094176	TTCCCAATTTGTTTT[G/T]TATATATATAAATAA	2177
rs565407117	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10047432	TATGTTTATTAACTG[A/G]TTATTTAGTCTGGGT	2177
rs565445624	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FANCD2, FANCD2OS	GRCh38.p7	3:10100142	GCAGTGAGCCATCAT[C/T]ACACTCCAGCCTGGA	2177
rs565491333	snp	C/T			utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101776	AGGATTCTAATGTAG[C/T]ATTATTTATTGGTTT	2177
rs565586202	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10029886	CCTCCCAGGTTCAAG[C/T]GATTTTCCAGCCTCA	2177
rs565586499	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082174	CTTAGTAAATGGTAC[C/T]ACCAGTTGCCTGAAC	2177
rs565590258	snp	G/T	6.59033e-05	0.00573997	intron-variant	FANCD2	GRCh38.p7	3:10078235	GACTTGGGCATAGTG[G/T]ATTTGGGAACAAAGG	2177
rs565595110	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10048650	AGGGAGGACTGTATT[G/T]GTGGAAAATGTTTAT	2177
rs565618776	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10063493	AGCCTTGCATGTAAA[G/T]CAATACATTTTTATT	2177
rs565629003	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10059195	ATTTTTGTATTTTCT[A/T]TAGAGATGAGGTTTT	2177
rs565703707	snp	G/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10071762	ATGAATAAGATCTAG[G/T]TGTTTTTGTATTTTT	2177
rs565721005	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095937	CCCAGGCCGGAGTGC[A/G]GTGGCACAATCTCTG	2177
rs565753068	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10053661	TAGATTTCCTAGTGT[G/T]TAGTAGTGGAAATGG	2177
rs565902593	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091267	TCTATTTTTAGTAGA[A/G]GCGGGGTTTTGTCGT	2177
rs565950016	in-del	-/A	0.0103295	0.0711199	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087623	ATCAGGGTCAAGTAT[-/A]AAAGAAATACTGGCC	2177
rs565986489	snp	A/G	0.00199481	0.0315187	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095397	TGTCTGTCCAAAGGC[A/G]GTTTATTCAGAGCAA	2177
rs565994663	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10053350	ACATGGGCACAGGAA[A/G]GGGAACATCACACTC	2177
rs566045120	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097464	GGGACGTTCCATGCT[G/T]AGAAAAAGAATTCAG	2177
rs566102090	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10066104	TGTGCTTCTCTAGCT[A/G]TTATGTCCCACCACT	2177
rs566126092	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084452	GTACCACCATGCCCA[G/T]CTGATTTTTCCTTTT	2177
rs566169097	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10061144	ATTATCAGTACTGCA[C/G]AAAGCCCTCTTCGGC	2177
rs566190998	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10049561	TAATTGGTGGGAGGT[A/G]GTGGGAAGGAGGTGA	2177
rs566246593	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10031559	AAAAAACAAAATGGC[A/C]TCATTAAGGGAGAAG	2177
rs566266781	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10050405	CAAGGCGGGCAAATC[A/G]CGAGGTCAGGAGATC	2177
rs566278820	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10048991	GTACTATATGGAGAA[A/C]ACCTTTAAAGCTTTT	2177
rs566342137	snp	A/G	0.00279162	0.0372561	intron-variant	FANCD2	GRCh38.p7	3:10038682	GCCTTCTGGGTTCAA[A/G]CGATTCTCCTGCCTC	2177
rs566444875	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093793	AGAATGCTACTTCGC[C/T]ACTCCTCAAGTTTCC	2177
rs566518051	snp	C/T	1.64741e-05	0.00286998	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087149	CCAGAGCGTCCATTA[C/T]TTGCAGAATTTCCAT	2177
rs566549167	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10065110	TCTGGCCAACGTGGC[A/G]AAACACTGTCTCTAC	2177
rs566554908	snp	G/T	8.24029e-05	0.00641831	intron-variant	FANCD2	GRCh38.p7	3:10063756	TGGGAAAGATTGGCA[G/T]CCCAAGGTTTAAACC	2177
rs566582594	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100405	TTGAGACGGAGTCTC[C/T]CTCTGTCGCCCAGGC	2177
rs566607234	snp	A/T			missense	FANCD2	GRCh38.p7	3:10048035	CATTTAAGTTTTTTG[A/T]CACGTACTGCCAGCA	2177
rs566627235	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10034218	AGTCCCAGCTACTTG[A/G]GGGGGCTGAGGCAGG	2177
rs566646823	snp	C/T	0.00398564	0.0444627	intron-variant	FANCD2	GRCh38.p7	3:10033136	TACAGTCAGGCCGGG[C/T]GCGGTGGCTCACGTT	2177
rs566668306	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10062781	GGTGGTGCTTCCCGG[A/G]TTCAAGCAATTCTCC	2177
rs566682767	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10059142	CCCCAGCCTTCCGAG[A/T]AGCCAGGACCACAGG	2177
rs566692910	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10063036	TCCATTTAATCTCTC[C/T]AATTAAATTATAAAG	2177
rs566702868	snp	A/G	1.64765e-05	0.00287019	intron-variant	FANCD2	GRCh38.p7	3:10042706	GATAAAGCAACTTAA[A/G]TGCCAATTGCTCTTC	2177
rs566712088	snp	A/G	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10070411	CCGGCCAGCTGCCCC[A/G]TCCGGGAGGTGAGGG	2177
rs566747571	in-del	-/C	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10070035	GTCTCTGCCCGGCCA[-/C]CCCATCGTCTGAGAT	2177
rs566768778	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10068434	TAGGAATAAGCTTAA[C/T]CAAAGAAGTGAAAGA	2177
rs566769898	snp	A/G	0.000158366	0.00889706	missense	FANCD2	GRCh38.p7	3:10034777	TTTTGTCTTGTGAGC[A/G]TCTGCAGGATGAGGA	2177
rs566847111	snp	A/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10024555	GAATTTGAGACCAAC[A/T]GGGCAACATAGTGAG	2177
rs566879974	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10066921	GTAGACATGGGCTTT[C/T]ACCATGTTGGCCAGA	2177
rs566926219	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10075480	CAAGCCCCCGTGCCC[A/G]GCCCCATAGCTTTAT	2177
rs566930292	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10035532	TTATCATATTCATAT[C/T]TACATTATCTCCCAT	2177
rs566958847	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10030873	CCACTGCCCTTCAGC[C/T]GGGGCAACAGAGCAA	2177
rs567046232	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081304	AAAGGAAAATGAGGA[C/G]AATTACTGAAGCAAC	2177
rs567106866	snp	A/G	1.92736e-05	0.00310426	intron-variant	FANCD2	GRCh38.p7	3:10046763	TTAATCTAAAACAGA[A/G]AGCTTTACAGCTCTC	2177
rs567177962	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087796	TGGGATTACAGGTGC[A/G]CACCACCGTGCCCAG	2177
rs567183176	snp	C/T	0.000461133	0.0151774	synonymous-codon	FANCD2	GRCh38.p7	3:10049430	TGAAGCTGAAGTTGA[C/T]ACTGCCTTAGATGTC	2177
rs567183643	snp	A/T	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10080864	CTGATTAGTTATGAT[A/T]GGGCTATATGTCTCA	2177
rs567267865	snp	G/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027457	TTACAAGATTAAAAG[G/T]TCATGTGATTCAGGC	2177
rs567292783	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086560	GATCCCAGCTCACTG[C/T]ACCCTCCACCTCCTG	2177
rs567306410	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027766	AAAAATTAGCCGGGC[A/G]TGGTGGCGGGCGCCT	2177
rs567327832	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10031990	AGTTGGTATTACAGG[C/T]GCACGCCACCACACC	2177
rs567411252	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10063423	GCCTGGACGACAGAG[C/G]AAGGCTCCATCTCAA	2177
rs567424125	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10077982	AAGGCTGGAATAGCT[A/G]TGATCTTGCCACTGC	2177
rs567433290	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085650	CCGCCTCAGCCTCCC[A/G]AAGTGCTGGGATTAC	2177
rs567440420	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10038809	TGGTCTTGAACTCCT[G/T]GCCTCATGTGATCTG	2177
rs567474382	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10039360	TGTGGATGGCAAGGT[A/G]GGCTTATGGACTTTA	2177
rs567487086	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10072383	TCCTGGGTTCAAGCA[A/G]TTCTCCTGCCACAGC	2177
rs567502367	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091901	AGTTCGAGACTAGCC[C/T]GGCCAACATGGTCAG	2177
rs567564558	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085052	ATCCAAAGATAGAAA[A/T]GTCAAGACTTGACTC	2177
rs567573921	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083759	CGAGCGTGGTTGCAG[A/G]CGCCTGTAGTCCCAG	2177
rs567613045	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10061929	GAACAATGAGAACAC[A/G]TGGACACAGGAAAGG	2177
rs567648067	snp	G/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10040702	CTTTTTATTGTACTA[G/T]AAGTATTTTTTTTAA	2177
rs567701848	snp	C/T	0.00835141	0.0640778	intron-variant	FANCD2	GRCh38.p7	3:10080506	CAGGGCACAGTGGCT[C/T]ACGCCTTTAACCCCA	2177
rs567708890	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10050790	CCCAGGAATGAGTTT[C/T]AAGAGTGAGGGATTG	2177
rs567734930	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10070800	GATAAATTCTTCTGC[C/T]TTGGGATCCTGTTGA	2177
rs567748795	snp	C/T	0.0103295	0.0711199	intron-variant	FANCD2	GRCh38.p7	3:10054815	TATCTTTTTTTCCCC[C/T]CCTTTCTTGGATCCC	2177
rs567779818	snp	C/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10050433	ATCAAGACCATCCTG[C/G]CTAACACGGTGAAAC	2177
rs567825484	snp	A/G	9.88484e-05	0.00702954	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088520	AGCAACATCTCTAAT[A/G]ACCAGCTCCATGCTC	2177
rs567867231	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10056130	GTGATCCGCCTGCCT[C/T]GGCCTCCCAAAGTGC	2177
rs567884981	snp	C/T	0.00279162	0.0372561	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098236	CTCAGAGAAGTTAAG[C/T]AATTTACCTAATGTC	2177
rs567895080	snp	A/G	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10055701	CCTATAGTCCCAGCT[A/G]CTTGGGAAGCTGAAG	2177
rs567898947	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094547	ACTCCTCAGGCCCAC[C/T]CTGGATCAAACCCAC	2177
rs567907901	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097541	TTCCGCCCGGCTCAC[C/T]GGCGGTCAGAGTTTA	2177
rs567942272	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10055191	ATAAAATAGACCGTT[A/T]AAGCTGTTTTTAAGG	2177
rs568021164	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10053288	CAAGAACAAAAAACC[A/G]CACACCGCATATTCT	2177
rs568043958	snp	C/T	1.70866e-05	0.00292284	intron-variant	FANCD2	GRCh38.p7	3:10043192	GTCACAATTTTCTGA[C/T]ATCCCACTGTCAGAG	2177
rs568071088	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081627	GTATTATTTCATTTG[A/C]TCTTGTACCCTCTGA	2177
rs568080434	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10076618	CAAGATCATAGCTCA[C/T]TGCAACCTTGAACTC	2177
rs568114661	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10054762	TGCTGGGATTACAGG[C/T]CTGAGCCACCGCACC	2177
rs568116280	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10031741	GATCATTGAGTCTCA[A/T]ATTTGGTGTGTATCA	2177
rs568178855	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10053658	TGATAGATTTCCTAG[C/T]GTGTAGTAGTGGAAA	2177
rs568206242	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10042851	CTTCCTGTGTAGTAC[C/T]TCACAGAATTCTGAA	2177
rs568224246	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100521	GGATTACAGGTGCCT[A/G]CAACCATGCCCGGCT	2177
rs568235770	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026523	GGCCCCGCTCCCCTG[C/T]GGCCTAATCTCTAAG	2177
rs568266808	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10052562	TAGCTCTGTCTCCTA[C/G]ACTGGAGTGCAGTTG	2177
rs568348064	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10056000	TCTCTTGCCTCAGCC[C/T]CCTGAGTAGCTGGGA	2177
rs568350566	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096885	TTACAAATTAATCTC[G/T]TATTGGGGGACCTGC	2177
rs568376132	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10058374	AATTTTTTTTCTTGT[A/G]TTTCTTGTCCTTTTG	2177
rs568428905	snp	C/T	0.00358779	0.0422022	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083713	CTAACACGGTGAAAC[C/T]CCGTCTGTACTAAAA	2177
rs568452291	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10089631	CCCACCACCACACCC[A/G]GCTAATTTTTGTATT	2177
rs568493521	snp	C/G	5.17219e-05	0.0050851	intron-variant	FANCD2	GRCh38.p7	3:10060442	TGTGGTTTAAGATCA[C/G]TTAATCTTGCTAACT	2177
rs568515612	snp	A/C/G/T	8.44426e-05	0.00649736	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090359	GTGAAAAAAATTGAG[A/C/G/T]CTGGCACAGCAGCAG	2177
rs568532917	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10050915	ACATGGAGAAAGCCC[A/T]CCTCTACTAAAAATA	2177
rs568572501	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10053850	TTCTGAGTGCAGTGG[A/G]GACACAGAATTGCCT	2177
rs568651838	snp	C/T	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10077205	AATATTGCACTCCAG[C/T]CTGAGCAACAGAGCG	2177
rs568746684	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10031296	ATCACGAGGTCAGGA[A/G]ATTGAGACCATCTTG	2177
rs568811940	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10099380	GTAATCCTAGCACTT[C/T]TTGAGGCCAAGGTAG	2177
rs568820965	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10033384	CCAGCCTGGGCGACA[A/G]GAGTGAGACTCCATT	2177
rs568837233	snp	C/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10062493	GTGATCCACCTGCCT[C/T]GGCCTCCCAAAGTGC	2177
rs568928778	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10064053	GGCTTTTCTGCCCTA[C/T]CCTGTCTCACGGCTC	2177
rs568930365	snp	C/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083169	GAGGCAGAGGTTGCA[C/G]TGAGCCAAGATTGCA	2177
rs568974390	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10062898	CCATGTTGGGGTTTC[A/G]CTATGTTGACCAGGC	2177
rs568997706	snp	A/G	0.000399281	0.0141238	intron-variant, missense	FANCD2, FANCD2OS	GRCh38.p7	3:10098886	TTCTAAGTTGGTGGA[A/G]CAGAACTTTGCCTAC	2177
rs569027995	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10040227	ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT	2177
rs569029566	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10055648	AAACCCCGTCTTTAC[C/T]AAAAATACAAAAAAT	2177
rs569041665	snp	A/G	0.0103295	0.0711199	intron-variant	FANCD2	GRCh38.p7	3:10060163	CAAGAACGAAAGTCC[A/G]TCTCAAAAAAAAAAA	2177
rs569070151	snp	C/T			synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085875	CCATGTCCTTAGTAG[C/T]CGACTGAAACAGGGA	2177
rs569084225	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083733	CTGTACTAAAAATAC[A/G]AAAAATTAGCCGAGC	2177
rs569137043	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10075089	AAGCACTTGCATTTC[A/C]GTAGTACATAGAGCA	2177
rs569142288	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10040608	ACTGTCATTCATTTG[A/G]AAAATAGTAATTGGT	2177
rs569166690	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10073686	ACATTTGTACTGTTC[A/G]TAGAATGAGTTTCAT	2177
rs569169518	snp	A/G	0.00636936	0.0560724	intron-variant	FANCD2	GRCh38.p7	3:10051223	GTCTCTACTAAAAAT[A/G]CAAAAAAATTAGCCG	2177
rs569258205	snp	C/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10046285	GTCTCGATCTCCTGA[C/G]CTTGTGATCTGCCCG	2177
rs569268842	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10030232	CGCCCAAGTAGCTGG[A/G]ATTACATGTACATGC	2177
rs569338907	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10041405	ATTGTGATGGAAGGC[C/T]TCTTGTTTCTACTTT	2177
rs569341483	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10035424	AAACTGTGCTTATTA[C/G]CCTAATACATCTGGC	2177
rs569367578	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10034108	GAGGGTGGATCACGA[A/G]GTCAGGAAATCGAGA	2177
rs569433760	snp	A/G	0.00716266	0.059414	intron-variant	FANCD2	GRCh38.p7	3:10028184	TTTTATAGCACTTAC[A/G]TAACTGTAGTTCAGT	2177
rs569528969	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10049313	GCCTTGGGGGTGAAT[A/C]CCTTTAGAATGGCCA	2177
rs569575835	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10053821	GTGATCAGCTAACCA[C/T]GAAACTGTTCAGTTT	2177
rs569603392	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10044389	AGCCAGATGATTGGC[C/T]GGGCGCGGTAGCTCA	2177
rs569662799	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10048708	TTTGTATTTTTACAT[A/G]TATTCTTCCTGTCAT	2177
rs569691735	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10038780	GAGATGGGGTTTCAC[C/T]GTGTTGGCCAGGCTG	2177
rs569698304	snp	C/T	0.00199481	0.0315187	intron-variant	FANCD2	GRCh38.p7	3:10072254	AAAATATCTCATGTG[C/T]GCCATAAATATATAT	2177
rs569704311	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10038030	GAATCTCACTCTGTT[A/G]CCCAGGCTAGAGTAC	2177
rs569719540	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090229	TTTTGGTTCCTGGTT[C/T]TTCCCAGGTAGTTCT	2177
rs569815961	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091819	AGCAACTACCACCGG[G/T]TGCAGTGGCGCACGT	2177
rs569816788	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10043776	CTGAATAAGGTGTAA[C/T]GTGTTTCGCTGATGT	2177
rs569889859	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097529	AACATGGTTCTGTTC[C/T]GCCCGGCTCACCGGC	2177
rs569954735	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091328	TCAAGCAATCCTCCC[A/G]CCTCAGCCTCCCAAA	2177
rs569959842	snp	A/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10075680	ATAGCATTAATTTTC[A/T]CCTGAAATTTACACG	2177
rs569980185	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10078949	TTTCGTCTCAAACAA[A/G]AAAAAAAGTCTACCT	2177
rs570051792	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10038435	CCAAAACTTTAGATA[C/T]AGGAGGCTCGAAGGA	2177
rs570126266	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10055584	TTGGGAGGCTGAGGC[A/G]GGCAGATCATGAGGT	2177
rs570126302	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10050172	TCTACTCAGCATTGA[C/G]AGATAACTCAGTAGG	2177
rs570138689	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084471	ATTTTTCCTTTTTTT[C/T]TTCTTTGGTAGAGAC	2177
rs570158924	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10053001	TAGAACTAGAAATAC[C/T]ATTTGACCCAGCCAT	2177
rs570180969	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10045137	TTGCCCTGAATACAC[A/G]CCCAATGTTTTCTCT	2177
rs570210918	snp	A/G	0.00199481	0.0315187	intron-variant	FANCD2	GRCh38.p7	3:10050401	AGGCCAAGGCGGGCA[A/G]ATCACGAGGTCAGGA	2177
rs570230434	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10066803	AATCTCGGCTCACTG[C/T]AACCTCCGCCTCCCA	2177
rs570254088	snp	A/G	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10031451	AGCTTGCAGTGAGCC[A/G]AGATCGCGCCACTGC	2177
rs570332092	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026687	CCCTCACCCGCTTCC[C/G]GATGAACTAATCCAG	2177
rs570355194	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100899	ATGTGGAGAAACCCC[A/G]TCTCTACCAAAATAC	2177
rs570443821	snp	C/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10047371	ATTATACCCAGCTTA[C/G]TACTAAATATAAGAT	2177
rs570454054	snp	A/G	3.29451e-05	0.00405851	missense, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10081409	GTTCAGGAGTACCAC[A/G]TAATGTCTTCCTGCT	2177
rs570459552	snp	A/G	0.000115334	0.00759299	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087257	TGCTCAGAACAAAGA[A/G]AAAATTGGTGATGGG	2177
rs570486054	snp	C/T			upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10024987	AAAAGGTCGAGGCTG[C/T]AGTGATTGAGGCTGC	2177
rs570512566	in-del	-/TTT	0.333261	0.235728	intron-variant	FANCD2	GRCh38.p7	3:10040034	GATCCACATACTTTC[-/TTT]TTTTTTTTTTTTTTT	2177
rs570537538	in-del	-/C	0.295854	0.245759	intron-variant	FANCD2	GRCh38.p7	3:10070387	AGGTCAGGGGGTCAG[-/C]CCCCCCGCCCGGCCA	2177
rs570580490	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10031274	TTTGGGTGGCCAAGG[C/T]GGGCAGATCACGAGG	2177
rs570587080	snp	A/G	3.30562e-05	0.00406534	intron-variant	FANCD2	GRCh38.p7	3:10052508	TCCAGGTAAGAGGCA[A/G]TATGTTGGGAAAGAT	2177
rs570622883	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10029609	TTTTACTAGGTTTTT[G/T]GGGAACAGGTGGTGT	2177
rs570631951	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10063136	ATAATTGGAAAGTGG[A/G]ACATAAAGCTAGTTC	2177
rs570660453	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10057690	TAAGATGGCACTCAC[A/C]ATCTTTGTGAAAAGT	2177
rs570691176	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10031004	AACTGAAGAGGAATA[A/G]TATAGGAAATTACTG	2177
rs570691535	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10036885	CTGTTGCCCAGGCTG[G/T]AGTGCCGTAGTACGA	2177
rs570700762	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10050295	GGCTTAAGAGACAAT[C/T]TGGTGTTAGAATTAA	2177
rs570726877	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10035387	GCTGTGATGGGTTTG[G/T]TAGGGTAATGTCTGT	2177
rs570749988	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025962	GAGACGTGAACCTAG[A/G]CAAACTGACACAACG	2177
rs570761297	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10030203	CCGGGTTCAAGCGAT[C/T]CTCCTGGCTCAGCCG	2177
rs570834893	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095454	CAGTCCTCTAGAGGG[G/T]AATCTCCGCATCTGA	2177
rs570836824	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10102423	GGTACAATTACAGGC[A/G]TGAGCCACCATGCCC	2177
rs570901187	snp	A/G	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10065146	ATACAAAAATTAGCC[A/G]GGCAGTGTGGCATGC	2177
rs570928093	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025276	CAAGTTTTTTGATGG[A/C]CTACCATGTGCCTTG	2177
rs570960687	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10059320	CGCCCAGCCTTGCCT[C/T]CATGTTTAAATCTTT	2177
rs570974010	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10033309	GGGCGCCTGAGTCAG[C/G]AGAATTGCTTGAACC	2177
rs570980736	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10033216	CAGGAATTTGCGACC[A/G]GCCTGGGCAACACGT	2177
rs571077672	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10042745	CAGACTAACTGAGAA[C/T]ACTGACTAATCCGGA	2177
rs571148016	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10076021	CAGGTGTGAGCCACT[A/G]CGCCCAGCCATATCT	2177
rs571185415	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10068243	TTATATTTGGAAAAG[C/T]CTAAAGACTCCACCA	2177
rs571185995	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086988	AGATGCTTGAAGAGG[A/G]TTGCTACTAAAGCAC	2177
rs571241821	snp	C/T	0.00119737	0.0244387	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098347	CATACTGTCCTTTAG[C/T]CTCCGCATGGCCATT	2177
rs571244921	snp	G/T	0.00279162	0.0372561	intron-variant	FANCD2	GRCh38.p7	3:10039518	ATAGATACTTCACCC[G/T]TTAAATTTCAGAAAA	2177
rs571255315	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10067669	CAGGCGTGGTTGTGG[A/G]CACCTGTAATCCCAA	2177
rs571259205	snp	C/G	0.00478085	0.0486577	intron-variant	FANCD2	GRCh38.p7	3:10074985	CTCTTCTGGTTCTTA[C/G]AAGTCAATGCCCTTT	2177
rs571307608	snp	A/C	1.91499e-05	0.00309429	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098669	CTTCTCCCCTATTAC[A/C]CTAAATGTGATCATT	2177
rs571387849	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10073541	AGACTTCAGGTCCTT[A/G]TTCCTGCCACACACT	2177
rs571393190	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10073145	GGGTTATAAAATTAC[C/T]TCTTCTACCTCTAGG	2177
rs571407774	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10045096	TTTAACTGTTTTTTT[C/T]TTTTTCCTGGAAGCA	2177
rs571505663	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10052552	AGACAGAGTCTAGCT[C/G]TGTCTCCTAGACTGG	2177
rs571522238	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10051177	CGAGGTCAGGAGATC[A/G]AGACCATCCCGGCTA	2177
rs571561486	snp	A/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10045357	GTATTTTTAGTGGAA[A/T]TGGGGCTTCATCATG	2177
rs571564737	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10069213	AAACACCAAAGTGAA[C/G]AGACAGCCCACAGAA	2177
rs571574759	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084866	CACAGCCATAATACA[A/G]TGAAAGCAGTGGTTT	2177
rs571575156	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10078448	CAAGCTCCGCCTCCC[A/G]GGTTCATGTCATTCT	2177
rs571649586	snp	A/G	0	0	intron-variant	FANCD2	GRCh38.p7	3:10034892	GTTGTTTCAAATTTC[A/G]TTTTTGGTGTAAGCT	2177
rs571656671	snp	C/T	0.00279162	0.0372561	intron-variant	FANCD2	GRCh38.p7	3:10030621	ACGGAAACTGTGGGC[C/T]GGGCACAGTGGCTCA	2177
rs571664921	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10046260	GGGTTTCACCGTGTT[A/G]GTCAGGATGGTCTCG	2177
rs571716562	snp	C/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10040272	CGATCTCCTGACCTT[C/G]TGATCCGCCCTCCTC	2177
rs571742493	snp	A/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10046336	GGGATTACAGATGTG[A/T]GCCACTGTGCCTGGC	2177
rs571760963	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10045877	AGTGCTGGGATTACA[A/G]GCGTGAGCCACCGTG	2177
rs571778733	snp	A/G	0.077417	0.180873	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093232	CGGGAAAGAGGCTGG[A/G]GTGCTCAAAGGAGCA	2177
rs571839609	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086443	CTAGACCATCACTGG[A/G]TCAGCAGTCAGTGCT	2177
rs571869727	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10074944	TACTACTAATAAGCT[A/G]CCTAGATTATTTTTG	2177
rs571921649	snp	A/G	0.0103295	0.0711199	intron-variant	FANCD2	GRCh38.p7	3:10071176	GATGGCTTTTATCCA[A/G]AGGACAGGCAATAAC	2177
rs571928194	in-del	-/C	0.00199481	0.0315187	intron-variant	FANCD2	GRCh38.p7	3:10075009	CCCTTTTCACTTTTT[-/C]CACAACATTTGTTCA	2177
rs571940621	snp	G/T			intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10099399	AGGCCAAGGTAGGAG[G/T]ATTGCTTGAGTCCGG	2177
rs572010952	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10080992	CAACTCATTTCTCCC[A/C]TCTGCTCCTACCTGG	2177
rs572046844	snp	A/G	1.67055e-05	0.00289006	intron-variant	FANCD2	GRCh38.p7	3:10064926	TTTTGAATGTTCATG[A/G]GGAATTCCACAGCTC	2177
rs572118928	snp	C/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10070294	TGGGAAGTGAGGAGC[C/G]TCTCCGCCCGGCAGC	2177
rs572126169	snp	C/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10038200	TTTCGCCATGTTGGC[C/T]AGGCTGGCCTCGAAC	2177
rs572143737	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10031229	GGAAAGGAGGCCAGG[C/T]ACGGTGGCTCACGCC	2177
rs572210439	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10037287	AATTTAAAACACTGT[A/G]TCAAAATAGTAAATA	2177
rs572252903	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10076314	CAAACCCTGTGTGTG[A/G]CATTCAAAGTCATTT	2177
rs572280975	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10047559	TATAGACCTACTTCA[A/G]ATTATAACCAAGGTG	2177
rs572288778	snp	G/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10042894	ATGTTCTATGACATT[G/T]CATTGGCTATTCTCA	2177
rs572293815	snp	C/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10047091	ATAAGCTAGGAATAG[C/T]GTTTTGCCAGCTGAA	2177
rs572357255	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101771	GGCTCAGGATTCTAA[C/T]GTAGCATTATTTATT	2177
rs572416277	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10044510	CCGTCTCTACTAAAA[A/G]TACAAAAAAAATTAG	2177
rs572436252	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10048964	TTGCTTGGAAACATG[C/G]AAGTCTAGCCTGTAC	2177
rs572437849	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10077657	CCTTGGGAGGCCAAG[A/G]CAGGAGGATTGCTCA	2177
rs572475084	snp	C/T	0.0023933	0.0345097	intron-variant	FANCD2	GRCh38.p7	3:10044053	GCCAGATAGCCTGCC[C/T]CTACTCACTCTGGCT	2177
rs572516539	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10071448	AGCAACCTAAGTGTC[C/T]ATCAGCGGGTGAATG	2177
rs572521379	snp	G/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10046305	TGATCTGCCCGCCTT[G/T]GCCTCCCAAAGTGCT	2177
rs572523258	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10040963	TGTTGGGCGGCTGAA[A/G]TGGGTGGGTCACTTG	2177
rs572528871	snp	C/G	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10068902	TTGGGGAAAGACACT[C/G]TCTTCAATAAATGGT	2177
rs572571155	snp	C/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10061999	GGGGAGGGATAGCAT[C/T]AGGAGATATACTTAA	2177
rs572581348	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10089175	CTGTAATCCCAGCTA[C/T]TTAGGAGGCTGAGGT	2177
rs572597474	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10045722	TTCTCCTGTCTCAGC[C/T]TCCCAAGTAGGTGGG	2177
rs572641019	snp	A/G	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10060036	GCCGGGCATGGTGGC[A/G]GGTGCCTGTAATCCC	2177
rs572680526	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10053928	GCTTTTGTTTGTGGG[C/T]GCCATTCACTGAAAA	2177
rs572717119	snp	A/C/T	0.00199481	0.0315187	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095670	CTTACTTTCAAGGAA[A/C/T]TCATCTATGTCTTAT	2177
rs572752401	snp	G/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10059566	CCAGCACTTTGGGAG[G/T]CCAAGACAGGCGGAT	2177
rs572764651	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100447	GGTGCAGTCTCAGCT[C/T]ACTGCAGTCTGTCTC	2177
rs572854380	snp	A/G	0.0138799	0.0821421	intron-variant	FANCD2	GRCh38.p7	3:10054381	tacgtgtatatacat[A/G]tatatacatatatat	2177
rs572855259	snp	G/T	0.0267878	0.112589	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092682	CTCCACCTCTTTCAT[G/T]TCTTTTTTTTTTTTT	2177
rs572858633	snp	A/T	0.00159617	0.0282053	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086590	GGGCTCAAGTGATTG[A/T]ACTGCCTCAGCCTCC	2177
rs572867296	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10057869	AAGATATTCTGTCAG[A/T]CATTCATGATCTGAA	2177
rs572924144	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10080210	GAGCTACAGTGCCCA[G/T]CAATTCATTCTTCTT	2177
rs572929608	snp	A/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10078846	GTGGTGCAGCTATAG[A/T]TCCAGCTACTTGGGA	2177
rs572933824	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085492	CACCTCCCGAGTTCT[A/G]GCGATTCTTCTGCCT	2177
rs572948443	snp	A/G	0.00199481	0.0315187	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092091	AATATCTGTATAGCT[A/G]TGTAATTCAAGAACT	2177
rs572956782	snp	G/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10050494	CGGGCATCGTGGCGG[G/T]CGCCTGTAGTCCCAG	2177
rs573066862	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10028157	CCTAGTAAGCCCTCA[C/T]AGAACCTGTACTTTT	2177
rs573085418	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087573	CAAAACGAGACATAA[A/T]TCATGAGGTTAATAA	2177
rs573087858	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098448	CTTAGAGTCACCAAT[A/G]CAGTCTAGCCTTTTA	2177
rs573120639	snp	A/G	0.0611083	0.163768	intron-variant	FANCD2	GRCh38.p7	3:10051603	ATGTCGAGAAGCATC[A/G]AGGAGGAGAGAATAA	2177
rs573146839	in-del	-/TTG			intron-variant	FANCD2	GRCh38.p7	3:10055865	TTCCATTCTTTGTTT[-/TTG]TTGTTGTTGTTGTGT	2177
rs573171368	snp	A/C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10062066	ATGGCACATGTATAC[A/C/G]TATGTAACAAACCTG	2177
rs573193058	snp	C/G	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10052187	AGTTGTAAGAATTTT[C/G]CCAGTTTATATCCAG	2177
rs573271971	snp	A/G	0.00279162	0.0372561	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093630	GGCAAAAGGGAGGAA[A/G]GAGGAGTAGATGATT	2177
rs573303858	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100663	TTTGGCGTGAGCCAC[C/T]GTGCACTGCCATACC	2177
rs573306335	in-del	-/T			intron-variant	FANCD2	GRCh38.p7	3:10038581	AATATATGCTTGCTT[-/T]TTTTTTTTTTTTTTT	2177
rs573363079	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10029757	CTTTCTCTTGAGTAT[C/T]CAAAGTCCATTATAT	2177
rs573392275	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10069714	AGTGATCCGCTAGCC[A/T]CAGCCTCCCGAGGTG	2177
rs573398821	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10070016	CCATCTAGGAAGTGA[A/G]GAGCGTCTCTGCCCG	2177
rs573414319	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087552	AAATTTATCTGAGAC[A/G]TTTGACAAAACGAGA	2177
rs573469906	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10068784	AACAGCATGGTGCTG[A/G]CACAAAAACAGATGC	2177
rs573493262	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10075111	CATAGAGCATCATGC[C/T]TGCTTTCAAATAACT	2177
rs573520348	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10035037	AAAGAGCCATCTGCT[C/T]ATTTCTGTATTTCTT	2177
rs573561625	snp	A/G	0.00279162	0.0372561	intron-variant	FANCD2	GRCh38.p7	3:10054570	CTCCCTGCAAACTCC[A/G]CCTCCCAGGTTCCCG	2177
rs573608049	snp	C/T	0.00199481	0.0315187	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084421	CAGCCTCCCAAGCAG[C/T]TGGGACTGCAGGCAT	2177
rs573659750	snp	A/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10060212	TAAACGCCTTTATAG[A/T]CTAGCTATATGGCTC	2177
rs573694583	snp	G/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081951	CTTTTGTTCCTCAGG[G/T]ACAGGCGTTGGGCTC	2177
rs573714806	snp	C/T	0.0023933	0.0345097	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096559	GAAGGTCACCTAAGC[C/T]CTCGTCTCTCAGTAA	2177
rs573754135	snp	C/T	0	0	upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026325	ACTCTGCTGCAGCGG[C/T]GAGCCCAGCTTATTG	2177
rs573839534	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10037476	TAGATTTTGCATACC[C/G]TTTAATCCTAATGTC	2177
rs573900454	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10038139	GGGATTACAGGTGTG[C/T]GCCACCACACCCAGC	2177
rs573906340	snp	A/G	3.29495e-05	0.00405877	missense	FANCD2	GRCh38.p7	3:10035225	CTTCTGGGGATTGAC[A/G]TACTGCAGGTAAGAC	2177
rs573927933	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027614	CCCTGCCTAAAAATC[A/C]CTTCTTCAGGCCGGG	2177
rs573948256	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10073866	GGGCAAGTGACTTGC[C/G]CAAAGTCACACAGTT	2177
rs573953089	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090749	AGACGTGCGCCACTG[C/T]GCCCGGTGGTAGTTG	2177
rs574018021	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084009	GCTTTTGTGTGTGTG[A/T]GAGAGACAGAGTCTC	2177
rs574027581	snp	G/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088306	AACGTGACAGCTTTT[G/T]GTAAGTTGCCTGTTA	2177
rs574054963	snp	A/G	0.00180448	0.029983	synonymous-codon	FANCD2	GRCh38.p7	3:10067292	CATTGTAGAATTGCA[A/G]ATAATCCTGGAAAAG	2177
rs574060125	snp	G/T	0.000283307	0.0118985	missense	FANCD2	GRCh38.p7	3:10073256	TTAATATAAAAGAAA[G/T]GAAACAAAAAACAGA	2177
rs574092196	in-del	-/T	0.0170713	0.0907977	intron-variant	FANCD2	GRCh38.p7	3:10035160	GGAAAACAGATTTCT[-/T]TTTTTTTTACAGTAT	2177
rs574123546	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10061762	ACAAAATAAATACTC[C/T]TCGCTGCCTTCATGC	2177
rs574190464	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10039073	TGTTCATATTTAGCA[C/T]GTCTTCTAGACATTT	2177
rs574201767	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10078597	CTGACCTTGTGATCC[A/G]CCCACCTTGGCCTCC	2177
rs574215319	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10067684	GCACCTGTAATCCCA[A/G]CTACTTGGGAGGCTG	2177
rs574266816	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091553	TCTCTTACTTGTCTA[A/G]CTCCGTTCTGGTTAG	2177
rs574273609	snp	A/C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10051197	CATCCCGGCTAAAAC[A/C/G]GTGAAACCCCGTCTC	2177
rs574322785	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10076146	TCACCCATTCTGCTT[C/T]TAGCAGTGTAATATA	2177
rs574334532	snp	A/C/G			intron-variant	FANCD2	GRCh38.p7	3:10050036	ATGATTGGAGGCAAG[A/C/G]CTGGTAAGACATAGG	2177
rs574353490	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093604	GTTACCTTCCGTGCC[A/G]TTCCTTACCAGGCAA	2177
rs574416410	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086865	GTTGTACATATTAGC[A/G]TGGTGCTTGGGTTTC	2177
rs574416558	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093985	TTCCCTCTTGGGAGT[A/C]AGTTATCCTCAGATA	2177
rs574426948	in-del	-/A	0.00517822	0.0506191	intron-variant	FANCD2	GRCh38.p7	3:10040134	CCGCCTCCTGGGTTC[-/A]CCCCATTCTCCTGCC	2177
rs574431883	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10042314	CCAGTTGAGAATTTA[A/G]GCTCTAAATGTAAGA	2177
rs574454997	snp	C/T	0.00517822	0.0506191	intron-variant	FANCD2	GRCh38.p7	3:10069855	GGCCTCCCAAAGTGC[C/T]GAGATTGCAGCCTCT	2177
rs574483745	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10075573	ATGTTTATATAGAAG[C/T]TGGGAGTAGAGGACA	2177
rs574529040	snp	G/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10080406	ACTCAGCTAATTTTT[G/T]TATTTTTTGTAAAGA	2177
rs574567648	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10041881	TGAGTTTCAGATGCT[A/G]TTCTATGGTAGAGTC	2177
rs574569158	in-del	-/T	0.0023933	0.0345097	intron-variant	FANCD2	GRCh38.p7	3:10029950	ACCATGCCCGGCTGA[-/T]TTTTTTTGTATCTTT	2177
rs574584183	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10078300	GCATTGTGTTTGGGT[C/T]ACTGGGTAGCATGGG	2177
rs574584630	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10047755	GAGTAATCTCAGAAT[A/G]ATGAAGGATTATTTT	2177
rs574620687	in-del	-/AGTC	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10077408	AAAAATACAAAAATT[-/AGTC]AGGCATGGTGGTGGG	2177
rs574625568	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10048360	CCAGGCTGGAGTGCA[G/T]TGGTGCTATCTCAGC	2177
rs574766679	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10031200	CATTCTGATTAAGGC[C/T]TTATTAGAAAGAGGG	2177
rs574820015	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10077021	CTCCCAAAGTACTGG[A/G]AGTTTGAGACCAGCC	2177
rs574867377	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082399	CTCAGTCCATTCTTC[A/C]CATGGCAGTAAGAGT	2177
rs574913507	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10045702	TGTCACCCGGGTTCA[A/C]GCGATTCTCCTGTCT	2177
rs574930710	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082942	AAATAAACATGTGAA[A/G]GGGGCCTGACATCGT	2177
rs574930949	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101702	TTTGTTCTTAAAGTG[A/G]GGTCTTTATTAACTT	2177
rs574939527	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10059429	ATAATAACAATAAAA[A/G]ATATTATTATTGAAT	2177
rs574944175	snp	G/T	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10058686	TCTTTGAACTCTGTA[G/T]TCTATTTCATTGGTC	2177
rs575011697	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10089042	AATCCCAGCACTTTG[A/G]GAGGCTGAGGCAGGA	2177
rs575027732	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10050480	ATACAAAAATTAGCC[A/G]GGCATCGTGGCGGTC	2177
rs575080915	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094803	CCAGGGCTAGAGTGA[A/T]GAATTAAGGATAGAA	2177
rs575102971	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10031365	AAAATTAGCCGGGCG[A/T]GGTGGTGTGCACCTG	2177
rs575163149	snp	A/G	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10078545	ATTTTTTGTAGAGAC[A/G]GGGTTTCACCGTGTT	2177
rs575167661	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026924	ATTATTAGAAGTCAT[C/T]ATAATCATCAAGAGT	2177
rs575183284	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027526	TCTCCTTGTTTCAGT[A/C]TGAGTATCTATTTGC	2177
rs575197743	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10079113	GCCAGGTATGGTGGC[A/G]CATGCTTGTAGTCCC	2177
rs575204533	snp	A/T	1.65241e-05	0.00287433	missense	FANCD2	GRCh38.p7	3:10064860	GTCCGGTGACCTCAC[A/T]GGAATCAGGCCAAAA	2177
rs575292685	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10055832	AAAAATAATAATAAA[G/T]AAATAAATAAATAAA	2177
rs575316437	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10061582	TTACCTCATAGAGTC[A/G]TTGAGAACATTAAAG	2177
rs575327958	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10069266	ATGTATCTGACAAGG[A/G]ACTAATAACTGGAAT	2177
rs575342861	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10031959	TCAAGTGATTCTCCT[C/G]CTCAGCCTCCCGAGT	2177
rs575356431	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10053985	GGAGGCCAAGGCAGG[A/C]GAATCACATGTGCCC	2177
rs575358183	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10055471	TATTTTCAAGGTTCA[C/T]GTAGGTTGTAGCATG	2177
rs575404713	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10074478	TTTTTATTAAAATTC[A/G]ATTAATATAGAAGAT	2177
rs575442418	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10039572	CATTTATTAAATAAA[C/T]TAAATATTTGGGAAG	2177
rs575491018	snp	C/G	0.00318978	0.0398085	intron-variant	FANCD2	GRCh38.p7	3:10045893	GCGTGAGCCACCGTG[C/G]CTGGCCTAGTAATTT	2177
rs575510044	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097848	TAAGAAATTACAAAA[A/G]TATTAATTTGGGGAA	2177
rs575519373	snp	G/T	0.0103295	0.0711199	intron-variant	FANCD2	GRCh38.p7	3:10056603	GTGGCGTGATCATAC[G/T]TCACTGCAGCCTGGA	2177
rs575541706	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10074004	AGGCTGGAGTGCAGT[G/T]GCACGATCTTGGCTC	2177
rs575550451	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10063337	AGCTACTCAGGAGGC[C/T]GGGGCAAGAGAATTG	2177
rs575583508	snp	G/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081020	TGGTGACACAGGTTT[G/T]ACTTGACTCCATTGC	2177
rs575593263	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FANCD2, FANCD2OS	GRCh38.p7	3:10099897	GATCCAGAAAGATCA[A/T]TTAGTATGAAAAGTC	2177
rs575601508	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10057339	AATAAAGTCAAATTT[A/T]TCTATTTCTTTTTCT	2177
rs575603964	snp	G/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10067121	AGATCTTGCTTTTCA[G/T]AGACATCTCTCAGCT	2177
rs575724746	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10071824	GAGTGCAGTGGCACA[A/G]TCTCGGCTTACTGCG	2177
rs575769620	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10102067	AAATCATGTCTCCTA[C/T]TGTAAGAACCAACTT	2177
rs575778928	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10029137	AAGCAAGCAAACCAG[A/G]GGCAAAGAAACAGTG	2177
rs575800972	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10076825	CTGCCTCCTGAGCTC[A/C]AGTGATTCTTCTGCC	2177
rs575810051	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10040369	ATGGTATACCTGTTA[C/T]GAGCGTGAAGTCTGG	2177
rs575817490	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100350	AACAGAATTTTGTAC[C/T]GGATTCCTGTTGAGA	2177
rs575860305	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10071258	GAATGTCAATTAGTA[C/T]AAGCACTATGGAGAA	2177
rs575893225	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10048246	TGTGTTCTGAGCTCT[A/G]AAATTCTCTGTCTGA	2177
rs575896189	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10033899	AGACGGAGTTTCACC[A/G]TGTTAGCCAGGATGG	2177
rs575901570	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10065722	TGATTGCTATATGAT[A/G]TGCAAATATTTTAAT	2177
rs575902263	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10079446	AGTAGCTGGGGACTA[C/T]AGGCGCGCGCCACCA	2177
rs575935226	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10076355	AGGATATTTAGGAAA[C/T]GCATCTTGGATCCAC	2177
rs576213468	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10031377	GCGTGGTGGTGTGCA[C/T]CTGTAGTCCCAGCTA	2177
rs576248785	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10042900	TATGACATTGCATTG[A/G]CTATTCTCATAACTC	2177
rs576286533	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10037389	TAGGCATGCTTGTAC[A/G]TTGCTAGTGAGCATA	2177
rs576343420	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097004	AAAGCTGGGCGTCCG[A/G]GGGAGACATCACACG	2177
rs576351350	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10078542	TGTATTTTTTGTAGA[A/G]ACGGGGTTTCACCGT	2177
rs576351555	snp	C/G/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090049	ATCTTCTCACTGTTA[C/G/T]TTCATTGCTTTTTCC	2177
rs576454493	in-del	-/G			intron-variant	FANCD2	GRCh38.p7	3:10073718	TGTTTGAAATTGCCT[-/G]GGCCACATGGATCCC	2177
rs576529341	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092846	ACAGGAACATGCCAC[C/T]ACACCCAGCTAATTT	2177
rs576535857	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10066570	GCTGGACTCATTTCT[G/T]TATGAAGAAATACTT	2177
rs576537705	snp	A/T	3.57207e-05	0.004226	intron-variant	FANCD2	GRCh38.p7	3:10073203	GCAATGATATTTGGC[A/T]AACATGATTATTAAT	2177
rs576558480	snp	A/T	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083240	TCAAAAAAAAAAAAA[A/T]CTGGGCCCCATGGCC	2177
rs576601472	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10044151	TCAAAGAAGCCAGGT[C/T]CCCACTGATGAGATG	2177
rs576610944	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10075920	TATTTTTAATAGAGA[C/T]GAGGTTTCACCGTTG	2177
rs576733617	snp	A/G	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10049653	CAAACACTTCTTTAT[A/G]CCTAACCTACAGGCT	2177
rs576740864	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FANCD2, FANCD2OS	GRCh38.p7	3:10099688	ACTTGAACCTGGGAG[A/G]TGGAGGTTGTGGTGA	2177
rs576792872	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10069384	TGGATATGTGAAAAG[A/G]TGCTCAACATCACTG	2177
rs576840847	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10049101	ATGGGAAAAAGAAAG[A/C]GGAAAACTACGCCAA	2177
rs576844684	snp	A/G	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10054421	TATACGTATATACAT[A/G]TATACATGTATATAC	2177
rs576875108	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10075210	TTTTTTGAGATGGAG[C/T]CTCTCTCTGTCGCCC	2177
rs576959583	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10052730	AAGGACATGAACAGA[C/T]ACTTCTCAAAAGAAG	2177
rs576985969	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10046129	CGCGATCTCGGCTCA[C/T]TGTAAGCTCTGCCTC	2177
rs577017799	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10080255	GGTCTACTTTTTGAG[A/T]CAGGGCTTTGCTCTG	2177
rs577033745	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10058036	TGCCTTCTTAATTCC[A/G]GCAAAGATCATTTTT	2177
rs577051351	snp	A/C/T	0.00318978	0.0398085	intron-variant	FANCD2	GRCh38.p7	3:10045413	GACCTCATGATCTGC[A/C/T]CGCCTCGGCCTCCCA	2177
rs577076153	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092850	GAACATGCCACCACA[C/G]CCAGCTAATTTTTCT	2177
rs577093127	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10029900	GCGATTTTCCAGCCT[C/T]AGTCTCCCGAGTAGC	2177
rs577135060	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10051351	CCGCCACTGCACTCC[A/G]GCCTGGGCGACAGAG	2177
rs577158769	in-del	-/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097265	TCTTATCAGGAGACA[-/G]GGTTTTGAGATCAAC	2177
rs577168333	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10031324	TTGGCTAACATGGTG[A/T]AACCCCGTCTCTACT	2177
rs577178552	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10030689	CAGATCACCTGAGGT[C/T]AGGAGTTCAAGATCA	2177
rs577192816	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10047697	AACTTCTTTGAGCTT[A/C]AAAGTCAATTATTAT	2177
rs577209479	snp	A/G	0.00398564	0.0444627	intron-variant	FANCD2	GRCh38.p7	3:10056583	GTTACCCAAGCTGCA[A/G]TGCAGTGGCGTGATC	2177
rs577218439	in-del	-/T	0.0023933	0.0345097	intron-variant	FANCD2	GRCh38.p7	3:10046425	AAAAATATTTCTGAG[-/T]TTTGTGAAAAGTGTA	2177
rs577235123	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10024615	TCTTTCAGTTACAAA[C/T]TACAAAGCTTTATCT	2177
rs577247004	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10051055	CATGCCATCACACTC[C/T]AGCCTAGGCGAGAAG	2177
rs577247097	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10057194	TTTTGTCGTTTTGAG[G/T]TATGGGAGTTATTTA	2177
rs577319789	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10064203	TGCTTTTTATGCACT[C/T]TCTCTTTTCTACTTC	2177
rs577363283	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101040	TGCCACTGCATTCCA[C/G]CCTGGTGACAGAGCA	2177
rs577363597	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094179	CCAATTTGTTTTTTA[G/T]ATATATAAATAAGAA	2177
rs577427524	snp	C/T	0.00199481	0.0315187	intron-variant	FANCD2	GRCh38.p7	3:10060833	TTGTTCCTTGAGGCC[C/T]CATTTGTAGAATCTA	2177
rs577455927	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10069733	CCTCCCGAGGTGCCG[A/G]GATTGCAGACGGAGT	2177
rs577471623	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10038922	GCGTTGATGTTATTA[A/G]TGTCTTACCTTTTAA	2177
rs577529817	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10062673	CTGTGGTTTTCTGAC[A/G]CTTGGAAACTACTGG	2177
rs577535611	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10076597	ACCCAGGCTGAAGTG[C/T]AGTGGCAAGATCATA	2177
rs577546023	snp	C/G	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091561	TTGTCTAGCTCCGTT[C/G]TGGTTAGCAGGCTGC	2177
rs577558626	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10032096	GTAATCAGCCTGCCT[C/T]GGCCTCCCAAAGTGC	2177
rs577568150	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10040434	AAGTTGACCATGATC[A/C]CTTAAGTTTCATTAA	2177
rs577610095	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084652	ATCAACTATATCTCA[C/T]TGAAGCTATGGTAGA	2177
rs577706778	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10074387	GGAATATTTAGGGAC[C/T]TGGGCTAGAGGAAGT	2177
rs577714114	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10066446	ATTTGATTACCACAT[C/G]TCTATTATGATACGG	2177
rs577763310	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097305	CAAAATTTATTAGGC[A/G]GGAATTTCCTCTTCC	2177
rs577824534	snp	C/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10031450	GAGCTTGCAGTGAGC[C/G]AAGATCGCGCCACTG	2177
rs577842154	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10073968	TTTTTGTTTTTGAGA[G/T]GGAGTCTCACTCTGT	2177
rs577911285	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10062127	AGTATAATAATAATT[A/T]AAAAAAAAATTCTTT	2177
rs577916564	snp	C/T	0.00398564	0.0444627	intron-variant	FANCD2	GRCh38.p7	3:10078643	ACGGGCATGAGCCAC[C/T]GCGCCCGGCCTCATC	2177
rs577981612	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10062584	TTATGAGTAACTGAA[A/G]AATTGCTTCTAGTCA	2177
rs578026710	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10067901	AATGTGATACCTCCT[A/G]TCAACAGAATGAAGG	2177
rs578068585	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10028369	GAGGGTCTTGAATCT[C/G]AGATGGAGAGTGATG	2177
rs578133386	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10045267	TCCGCCTCCTGGGTT[A/C]ACGCCATTCTCCCGC	2177
rs578174765	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10034247	GGAGAATCATTTGAA[C/T]CCAGGAGGCGGAAGT	2177
rs578180317	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10045254	GCTCACTGCAAGCTC[C/T]GCCTCCTGGGTTCAC	2177
rs578196227	in-del	-/A			intron-variant	FANCD2	GRCh38.p7	3:10030910	ATCTCAAAAAAAAAA[-/A]GGAAGTTGTGAAGCT	2177
rs578201085	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085159	TTTTGAAGAAGACTA[C/T]ATATCTCTAAAATAT	2177
rs578216759	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10045525	AAATTACTCCATCAT[A/T]ATTTATTGAACCTTT	2177
rs578227542	snp	G/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10040308	CCCAGAGTGCTGGGA[G/T]TACAGGCATGAGCCA	2177
rs587778329	snp	C/G			missense	FANCD2	GRCh38.p7	3:10072943	CACCTCATACTGTTA[C/G]TGCTATTTCAGCAAA	2177
rs587778330	snp	C/T	1.65059e-05	0.00287275	FANCD2, FANCD2OS	3	allele_origin=T(germline)/C(germline)	3:10081112	TAGAACAAAGGAAGC[C/T]GGAATATTGGATTCT	2177
rs587778331	snp	A/G	0.000247502	0.0111216	FANCD2, FANCD2OS	3	allele_origin=G(germline)/A(germline)	3:10081113	AGAACAAAGGAAGCC[A/G]GAATATTGGATTCTC	2177
rs587778332	snp	C/T			missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087198	CAGTGTGCTCTTTAT[C/T]TCATCAGACTTTTGA	2177
rs587778333	snp	A/G			missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092211	CTCCTCTACTGGAAC[A/G]TGGCTGTTCGAGACT	2177
rs587778334	snp	G/T			missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101207	GTGAAGAAGACGAAG[G/T]AAGTGCTGGAGAAAA	2177
rs745305575	snp	C/T	6.59065e-05	0.00574012	synonymous-codon	FANCD2	GRCh38.p7	3:10046666	GCTAAGAAATAAGAT[C/T]CGATCAGGCTGCATT	2177
rs745320152	snp	C/T	3.29598e-05	0.00405941	intron-variant	FANCD2	GRCh38.p7	3:10041614	TTTTTCTTTTTCTAC[C/T]ATTCACAGTGACCTA	2177
rs745331502	snp	A/C			utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101374	GGATCCTTTTTTGTT[A/C]CTCTTTTTTTTTTTT	2177
rs745349478	snp	C/T			upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025154	GAGACAGTGGTCTCA[C/T]TGTGTTGCCCAGGCT	2177
rs745373058	snp	A/G	1.65108e-05	0.00287317	missense, downstream-variant-500B	FANCD2, FANCD2OS	GRCh38.p7	3:10081109	TTATAGAACAAAGGA[A/G]GCCGGAATATTGGAT	2177
rs745396328	snp	A/T	1.64857e-05	0.00287099	intron-variant	FANCD2	GRCh38.p7	3:10041718	TATTGAAGGTAGAAA[A/T]GACTCAGCTTTCCAG	2177
rs745414816	snp	C/G	1.64827e-05	0.00287073	missense	FANCD2	GRCh38.p7	3:10063870	TACTATGATGAATTT[C/G]CCAACCTGATCCAAC	2177
rs745429168	in-del	-/AAG			intron-variant	FANCD2	GRCh38.p7	3:10051603	ATGTCGAGAAGCATC[-/AAG]GAGGAGAGAATAAAA	2177
rs745439789	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10060835	GTTCCTTGAGGCCCC[A/G]TTTGTAGAATCTAAA	2177
rs745444413	snp	C/T	1.64741e-05	0.00286998	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094332	TGAAGCAATGTATGC[C/T]GCTCCTAGACTTCAG	2177
rs745472884	snp	A/G	1.64743e-05	0.00287	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096450	CTTTCTGGCTGGGCA[A/G]TCTAAAAAACCGGGA	2177
rs745498971	snp	A/G	1.66012e-05	0.00288103	missense	FANCD2	GRCh38.p7	3:10060294	ATCATCTCATTGCAG[A/G]ATGACATGCACTTGG	2177
rs745528628	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10044983	AATGACTGTATTCTG[G/T]TCTAATAACTCAGTT	2177
rs745540569	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10064098	CTTCACTTAATAACA[A/G]TCACGATAGTAAAGA	2177
rs745562746	snp	A/G	1.64838e-05	0.00287083	missense, downstream-variant-500B	FANCD2, FANCD2OS	GRCh38.p7	3:10081192	ACTGCTGACCCCAAT[A/G]TGTAACCACCTGGAG	2177
rs745573504	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10058743	ACACTGTTTTGACTG[A/C]TGTAGCTTTGTATTA	2177
rs745620718	snp	C/T	3.29886e-05	0.00406118	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096503	TGCTAGTGATAATCC[C/T]CTACTCTTATTCTTT	2177
rs745657721	snp	C/T			utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101574	TATTTTTAGTAGATA[C/T]GGGGTTTTACCATGT	2177
rs745660691	in-del	-/TTAATT	1.64741e-05	0.00286998	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088814	TGGGTCAAATATTTG[-/TTAATT]ACTCTCAATGCAGTA	2177
rs745686606	snp	A/G	1.65938e-05	0.00288039	intron-variant	FANCD2	GRCh38.p7	3:10036367	ATTATGGAATGTTCA[A/G]AGTACCCTGATGTAC	2177
rs745700100	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10067941	ACATGATATTTAAAT[A/T]GATGCTTAAAAAAAT	2177
rs745705212	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10050491	AGCCGGGCATCGTGG[C/T]GGTCGCCTGTAGTCC	2177
rs745760607	in-del	-/A			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094705	TCTCAGAAATGATTT[-/A]TAAAAAAAAAAAAGC	2177
rs745761701	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10036078	GTTGGAAAGAGAATT[A/T]TACATTTCTTTTTTT	2177
rs745765337	snp	C/G	0.000181373	0.00952122	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088540	GCTCCATGCTCTGCT[C/G]TGGTGAGATGTTTGG	2177
rs745779297	snp	G/T	1.65072e-05	0.00287286	missense	FANCD2	GRCh38.p7	3:10043113	CCATCACGGTTACAG[G/T]CTTCCCAAGTAAAGT	2177
rs745841768	snp	A/G	0.000281013	0.0118502	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098740	AGAGATTAAGTCCCA[A/G]AATTCCCAGGAGAGC	2177
rs745855901	snp	A/T	1.64846e-05	0.0028709	intron-variant	FANCD2	GRCh38.p7	3:10036283	CCTATGTCTTCTTTT[A/T]TAGCCTGCCATTATC	2177
rs745901068	snp	G/T	3.29598e-05	0.00405941	intron-variant	FANCD2	GRCh38.p7	3:10063762	AGATTGGCAGCCCAA[G/T]GTTTAAACCATTCTT	2177
rs745920972	in-del	-/AATAAATAAATA			intron-variant	FANCD2	GRCh38.p7	3:10055826	CAAAAAAAAAATAAT[-/AATAAATAAATA]AATAAATAAATAATT	2177
rs745930696	snp	C/T	3.29533e-05	0.00405901	stop-gained, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092220	TGGAACATGGCTGTT[C/T]GAGACTTCAGTATCC	2177
rs745937059	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10029025	TAACATAGTCTGTAC[C/G]CTTAAAAAACTTTAT	2177
rs745952317	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093810	CTCCTCAAGTTTCCT[C/T]CCAAGTGGATGGTGC	2177
rs745968833	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10048882	GAGTGACAGTATAAA[A/G]GGAGAATGGCATCTA	2177
rs745982822	snp	A/G	1.64743e-05	0.00287	intron-variant	FANCD2	GRCh38.p7	3:10042692	TCCCATCACACCTAG[A/G]TAAAGCAACTTAAGT	2177
rs746015615	snp	C/T	1.64803e-05	0.00287052	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101253	TGAGAGTTATGATGA[C/T]TCTGATTAGACCCCA	2177
rs746017476	snp	A/G	1.84975e-05	0.00304112	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090410	ATAATAGTCACTTCA[A/G]GAAGTGGACTTTGGA	2177
rs746020754	snp	C/G	1.64768e-05	0.00287021	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085903	GGAGAACACAGCCAG[C/G]CTTTGGAGGAACTAC	2177
rs746053143	snp	G/T	4.9458e-05	0.00497258	splice-donor-variant	FANCD2	GRCh38.p7	3:10028722	CAGAAGATGCCTCCA[G/T]TAAGTATCTAGTCAT	2177
rs746069930	snp	A/G	1.65455e-05	0.00287619	missense	FANCD2	GRCh38.p7	3:10062182	TTGACCCAAGAGAGA[A/G]CCAACCTGAGCGATG	2177
rs746132082	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10066940	ATGTTGGCCAGACTG[A/G]TCTCAAACTCCTGGC	2177
rs746135951	snp	C/T	1.64732e-05	0.0028699	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085809	TTACCTTGACTTCCT[C/T]AGGAGTGGATTTTCT	2177
rs746194721	snp	A/G	1.64795e-05	0.00287045	intron-variant	FANCD2	GRCh38.p7	3:10078047	TGAAATGACTAGGAC[A/G]TTCCTGGAACTAATC	2177
rs746215073	in-del	-/T	3.09655e-05	0.00393469	intron-variant	FANCD2	GRCh38.p7	3:10062125	AAAGTATAATAATAA[-/T]TTAAAAAAAAATTCT	2177
rs746223604	snp	A/G	1.64762e-05	0.00287016	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088423	AGTTCCCATATGTAA[A/G]ATTCCTTTGTCTTCT	2177
rs746259041	in-del	-/TTTG	1.65146e-05	0.0028735	intron-variant	FANCD2	GRCh38.p7	3:10064334	CTCTGCACTGCCCTT[-/TTTG]TTTGTTTGCTTCCTG	2177
rs746262817	snp	A/G	1.64746e-05	0.00287002	missense	FANCD2	GRCh38.p7	3:10039741	CACCACCAAGATCAT[A/G]CAGCTGATCAGTATT	2177
rs746265846	snp	A/G	1.64727e-05	0.00286986	missense	FANCD2	GRCh38.p7	3:10065473	CATAACGGAAACTTG[A/G]AGGAGATTGATGGTC	2177
rs746384555	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10058484	CTCTTAAATTTAGGT[C/G]TTTGATCCACTTTGT	2177
rs746388305	snp	A/G	6.61715e-05	0.00575164	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10098995	CCCAGAAGAAACAAC[A/G]ACACAATCTTAGAAT	2177
rs746389067	snp	A/G	3.29516e-05	0.00405891	missense	FANCD2	GRCh38.p7	3:10074624	TCTTCTCTATTCTAC[A/G]TTGTGGACTTGTGAC	2177
rs746411923	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10040620	TTGAAAAATAGTAAT[C/T]GGTAGGGAAGTATTG	2177
rs746436516	in-del	-/T	1.65809e-05	0.00287926	intron-variant	FANCD2	GRCh38.p7	3:10049353	TGTTTTACACTGTTC[-/T]GTTGACTCTCCCCTG	2177
rs746442733	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10073527	GCAAAGTTCAGATTA[A/G]ACTTCAGGTCCTTAT	2177
rs746456122	snp	A/G	6.04735e-05	0.00549846	intron-variant	FANCD2	GRCh38.p7	3:10067325	CTTGGCAGGTAAGAG[A/G]AGTGTCCTATACTGG	2177
rs746471820	snp	C/G	3.29995e-05	0.00406185	intron-variant	FANCD2	GRCh38.p7	3:10063938	TGTCTTTTCTTAAAG[C/G]AATAAAGCATGAGAG	2177
rs746484550	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10037514	CTCATTTATCCTAAG[A/T]TAATAACTGTGAATG	2177
rs746492664	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10075122	ATGCTTGCTTTCAAA[G/T]AACTTCTAATCTAAT	2177
rs746501818	snp	A/G	3.29522e-05	0.00405894	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094359	TCAGTTTTAGAAAAC[A/G]CCGGGTAAGAGCTAA	2177
rs746511202	snp	A/G	3.5743e-05	0.00422732	intron-variant	FANCD2	GRCh38.p7	3:10034658	CAAATATTAAACTAA[A/G]AATTTTATTCTTTTT	2177
rs746529366	snp	C/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087679	TTGAGACAGAGTCTC[C/G]TTCTGTCACCCAGGC	2177
rs746537039	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10078904	CAGTGAGCTGAGATT[G/T]CACCAGTGCACTCCA	2177
rs746537955	snp	C/G	1.64727e-05	0.00286986	missense	FANCD2	GRCh38.p7	3:10049403	CTTAGTGACCCATAT[C/G]TGCAGTGGGAATGAA	2177
rs746538741	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10074340	TTGATGTGTGACTTG[A/T]ATCCCCATCTTAAAT	2177
rs746640591	snp	A/T	1.74376e-05	0.00295271	intron-variant	FANCD2	GRCh38.p7	3:10046733	TACTTAGTAAGTGTC[A/T]GAGACTATTGATTTT	2177
rs746666831	snp	A/T	1.7219e-05	0.00293414	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095172	ATCAGGACATTTCAT[A/T]GAGCATTTATAAACT	2177
rs746701320	snp	A/C			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081890	AAGGAAGTGGAAGGT[A/C]CAACATGGACAAAAG	2177
rs746722465	snp	A/G	1.64735e-05	0.00286993	missense	FANCD2	GRCh38.p7	3:10042563	TTAATTTTTAGGTTC[A/G]CCAGTTGGTGATGGA	2177
rs746726118	snp	A/G	8.26439e-05	0.00642769	synonymous-codon	FANCD2	GRCh38.p7	3:10060308	GGATGACATGCACTT[A/G]GTGATAAGAAAGCAG	2177
rs746732289	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10066811	CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCAGG	2177
rs746739014	snp	C/T	1.65198e-05	0.00287395	intron-variant	FANCD2	GRCh38.p7	3:10034460	CCAGCTCTTCTTTTT[C/T]CTGCATAGCTGTGGA	2177
rs746782750	snp	G/T			intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10099021	AGAATCACTCCTGAG[G/T]ATCTCGAGTTGTGGC	2177
rs746795320	snp	A/G			missense	FANCD2	GRCh38.p7	3:10064842	ACTTTGCAAAAGATG[A/G]GGGTCCGGTGACCTC	2177
rs746834645	snp	C/T	4.94336e-05	0.00497135	missense	FANCD2	GRCh38.p7	3:10046671	GAAATAAGATTCGAT[C/T]AGGCTGCATTCAAGA	2177
rs746855313	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10066072	CCCTAGAAGTCTTCA[A/C]CAAGCACTAACCCCC	2177
rs746871581	snp	A/T	1.65091e-05	0.00287303	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098748	AGTCCCAAAATTCCC[A/T]GGAGAGCACAGCAGA	2177
rs746902945	snp	C/T			intron-variant, downstream-variant-500B	FANCD2, FANCD2OS	GRCh38.p7	3:10099943	GCTCACACCTGTAAT[C/T]GTAGCACTTTGTGAG	2177
rs746917523	snp	C/T	1.66543e-05	0.00288563	intron-variant	FANCD2	GRCh38.p7	3:10036378	TTCAAAGTACCCTGA[C/T]GTACTTAAGTTCTCT	2177
rs746943331	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10041065	TGGGCGTGGTGGTAC[A/G]CACTTATAATTCTAG	2177
rs746952691	snp	A/T	1.64963e-05	0.00287192	missense, downstream-variant-500B	FANCD2, FANCD2OS	GRCh38.p7	3:10081115	AACAAAGGAAGCCGG[A/T]ATATTGGATTCTCAC	2177
rs746964566	snp	A/T	0.000135071	0.0082169	intron-variant	FANCD2	GRCh38.p7	3:10052524	TATGTTGGGAAAGAT[A/T]TTTTTTTTTTTGAGA	2177
rs746965013	in-del	-/G	1.64822e-05	0.00287068	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093349	ACTGGGCCCTGTTTC[-/G]ATATTTATTCTTCCT	2177
rs746970126	in-del	-/A			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10028053	CCCTGTCTCTACTAA[-/A]AAAAAAAAAAAAAAA	2177
rs746985045	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10050452	ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA	2177
rs746987307	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10038631	TGTCACCCAGGCTGG[A/G]GTGCAGTGGCACGAT	2177
rs747006885	snp	C/T	1.66815e-05	0.00288799	synonymous-codon	FANCD2	GRCh38.p7	3:10039318	ACCTCGACTCATTGT[C/T]AGTCAACTAAAATGG	2177
rs747008456	in-del	-/AGG			intron-variant	FANCD2	GRCh38.p7	3:10067704	TTGGGAGGCTGAGAC[-/AGG]AGAATCGCTTGAACC	2177
rs747044380	snp	C/G	0.000181658	0.00952868	intron-variant	FANCD2	GRCh38.p7	3:10048083	ATTTTGGCAAGGAGG[C/G]AACACAGAAAGGGAA	2177
rs747075480	in-del	-/TCCTGGATG	1.64738e-05	0.00286995	cds-indel	FANCD2	GRCh38.p7	3:10041661	CACTCACTGTCCCAA[-/TCCTGGATG]TCCTTTCAAGCCTCC	2177
rs747078545	snp	A/C/G	4.94542e-05	0.00497243	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085930	CTACTCAGGTGAGTC[A/C/G]TAACTACATAGCCAA	2177
rs747093067	in-del	-/TC			intron-variant	FANCD2	GRCh38.p7	3:10076297	TCTTTTTTTTTTTTC[-/TC]CCAAACCCTGTGTGT	2177
rs747132291	snp	C/T	1.711e-05	0.00292484	intron-variant	FANCD2	GRCh38.p7	3:10043194	CACAATTTTCTGACA[C/T]CCCACTGTCAGAGTT	2177
rs747139694	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10057348	AAATTTATCTATTTC[G/T]TTTTCTTTTTCTTTC	2177
rs747141763	snp	G/T	1.65236e-05	0.00287429	intron-variant	FANCD2	GRCh38.p7	3:10073412	ACATCCCAGTGAGAT[G/T]AACAGAAACCCAGCT	2177
rs747148572	in-del	-/T			downstream-variant-500B, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10102144	CTTGATCTTCTTTCC[-/T]TTTTTTTTTTTTTTT	2177
rs747157259	snp	A/G	3.30606e-05	0.00406561	missense	FANCD2	GRCh38.p7	3:10032915	GACAGCATCTTTGTA[A/G]AGCTTCTTAAGATAT	2177
rs747161300	in-del	-/TAGA			intron-variant	FANCD2	GRCh38.p7	3:10071739	CTTCAAAAATATAAT[-/TAGA]TAGAATGAATAAGAT	2177
rs747164592	snp	C/T	1.64735e-05	0.00286993	missense	FANCD2	GRCh38.p7	3:10064742	AGTGACTTTCCATTT[C/T]CTGTGAAAGCACTGT	2177
rs747177755	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10048270	TGTCTGAAATTAAGA[A/T]CCAGATCTAGTCCAT	2177
rs747225209	snp	C/T	1.64819e-05	0.00287066	missense	FANCD2	GRCh38.p7	3:10063837	TGCAGTGAGCAGTCT[C/T]CTCAGGCCTCTGCAC	2177
rs747310854	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10033132	ATGGTACAGTCAGGC[C/T]GGGCGCGGTGGCTCA	2177
rs747322758	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084155	CCTGCCACTGCACCT[A/G]GCTAATTTTTGTATT	2177
rs747329331	snp	A/C	6.61802e-05	0.00575202	missense	FANCD2	GRCh38.p7	3:10065882	GTCCTATATTCCTAA[A/C]TGACCTGGAGCCTGG	2177
rs747338479	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10071486	TGTGGTCCGTATACA[C/T]AATGGAGTACTATTC	2177
rs747362056	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10032216	ACAGCTTGAGAGACA[C/T]TGGCTAGTTTAGTAT	2177
rs747371509	snp	C/T	1.65359e-05	0.00287536	utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101266	GACTCTGATTAGACC[C/T]CAGATAAATTGTTGC	2177
rs747383951	in-del	-/A			intron-variant	FANCD2	GRCh38.p7	3:10050622	GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	2177
rs747407911	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082858	GTCTGTCATTTTTAT[A/G]TCCTCATTACTTAAA	2177
rs747410472	snp	C/T	9.89511e-05	0.00703319	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093270	GCCTTGGTTTCTTGT[C/T]TTTCACCTCTCCAGG	2177
rs747412191	snp	A/C	3.33656e-05	0.00408432	intron-variant	FANCD2	GRCh38.p7	3:10032814	TTGCCATATTCTTGA[A/C]AATTTTTCTATTTTC	2177
rs747421602	snp	C/T	1.64795e-05	0.00287045	intron-variant	FANCD2	GRCh38.p7	3:10063771	GCCCAAGGTTTAAAC[C/T]ATTCTTCCTCTTTGC	2177
rs747433455	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090202	ATTTAGAGAGGTAGG[A/G]AAGGAAGCTACTTTT	2177
rs747438763	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10045744	GTAGGTGGGATTACA[C/G]GTGTGTGCTACTTTG	2177
rs747450518	snp	C/G	1.64732e-05	0.0028699	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085837	TCTCAACCTGAAAAT[C/G]AGAATTTACTGTATT	2177
rs747469438	in-del	-/T	1.6513e-05	0.00287336	frameshift-variant	FANCD2	GRCh38.p7	3:10064850	AAGATGGGGGTCCGG[-/T]TGACCTCACAGGAAT	2177
rs747512731	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10072509	GTCTCAAACTCCTGA[C/T]CTCAGGTGATCCGCG	2177
rs747525433	snp	A/G	1.64727e-05	0.00286986	missense	FANCD2	GRCh38.p7	3:10065485	TTGGAGGAGATTGAT[A/G]GTCTACTAGGTATGG	2177
rs747565337	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097659	CTGTACAATTTGTGT[A/G]GTTAACGCAATTATT	2177
rs747575196	snp	C/G	1.64798e-05	0.00287047	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092235	CGAGACTTCAGTATC[C/G]TCATCAACTTGATAA	2177
rs747600237	snp	A/C	1.66183e-05	0.00288251	intron-variant	FANCD2	GRCh38.p7	3:10049510	TCTTTGTAAAGGTAT[A/C]TTATTGGCTTCTTGT	2177
rs747604554	in-del	-/TT	1.64727e-05	0.00286986	frameshift-variant	FANCD2	GRCh38.p7	3:10065441	TCCGGTTACTGAGAC[-/TT]TGTGTGGAGAGACAG	2177
rs747616219	snp	A/G	1.65277e-05	0.00287464	intron-variant	FANCD2	GRCh38.p7	3:10039873	TCTGTCATCATCTAA[A/G]TGAGGCTCAGCTATG	2177
rs747632960	snp	C/T	1.65425e-05	0.00287593	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096293	GCATGATGATAAACT[C/T]ACAAAAGATGGATGT	2177
rs747677405	in-del	-/TAA			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10028050	AAACCCTGTCTCTAC[-/TAA]AAAAAAAAAAAAAAA	2177
rs747681778	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10038209	GTTGGCCAGGCTGGC[C/T]TCGAACTCCTGACCT	2177
rs747687828	snp	A/G/T	4.9473e-05	0.00497337	synonymous-codon	FANCD2	GRCh38.p7	3:10052404	CATTTTAGATTATCT[A/G/T]GATAACATATCCCCT	2177
rs747697451	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084580	GCTGGCATTAGAGGC[A/G]TGAGCCACCATACCT	2177
rs747709662	in-del	-/AGA	1.64746e-05	0.00287002	intron-variant	FANCD2	GRCh38.p7	3:10078210	AAGGTTAGTGTAGGC[-/AGA]AGCATAGGACTTGGG	2177
rs747751298	in-del	-/TTG			intron-variant	FANCD2	GRCh38.p7	3:10029778	TCCATTATATCATTC[-/TTG]TTGTTGTTGTTGTTG	2177
rs747786350	snp	C/T	3.29462e-05	0.00405857	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088454	TTTCTAACAGCTTCC[C/T]TTGCCAGACAATTCC	2177
rs747832380	snp	A/G	1.64738e-05	0.00286995	synonymous-codon	FANCD2	GRCh38.p7	3:10064391	CTGTAATGATTTCCA[A/G]GATGCCTTCGTAGTG	2177
rs747833438	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10065161	GGGCAGTGTGGCATG[C/G]ACCTATAATCCCAGC	2177
rs747840074	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10074192	CTCGTGATCCACCCA[C/T]GTCAGCCTCCCAAAG	2177
rs747876902	snp	A/G	1.67262e-05	0.00289185	intron-variant	FANCD2	GRCh38.p7	3:10035133	AAAGCATTAAAACAA[A/G]GAAAGCAAAGTGGAA	2177
rs747880206	snp	A/G			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026956	AGTATAGGTGGTGAA[A/G]AGCGCAGGTGCTGAA	2177
rs747906848	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10077683	GCTCAAGCCCAGGAG[G/T]TTGAAACCAGCCTGG	2177
rs747927128	snp	A/C			upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10024811	CATGATATTCAACTC[A/C]ATTTCTACAAAACTA	2177
rs747942447	snp	C/T	1.69602e-05	0.00291201	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090366	AAATTGAGCCTGGCA[C/T]AGCAGCAGACTCGCA	2177
rs747942498	snp	A/G	1.64841e-05	0.00287085	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081305	AAGGAAAATGAGGAC[A/G]ATTACTGAAGCAACT	2177
rs747977469	snp	A/C	4.94189e-05	0.00497062	missense	FANCD2	GRCh38.p7	3:10042580	CAGTTGGTGATGGAT[A/C]AGTTGTCGTCTATTA	2177
rs748006255	snp	A/G	0.00013183	0.00811775	splice-acceptor-variant	FANCD2	GRCh38.p7	3:10047915	ACTCTTCCCCACTCA[A/G]GGTTCTTAAGGATAT	2177
rs748023774	snp	G/T	1.68499e-05	0.00290253	intron-variant	FANCD2	GRCh38.p7	3:10060418	GGTACACGTGGAGAT[G/T]CTGACTTCTGTGGTT	2177
rs748026680	snp	A/G	2.24535e-05	0.00335056	intron-variant	FANCD2	GRCh38.p7	3:10067348	TATACTGGTAGTACT[A/G]CTAGGCCAGTAGTGA	2177
rs748111595	snp	C/T	1.64738e-05	0.00286995	intron-variant	FANCD2	GRCh38.p7	3:10039230	TAATGCTTGCTGTTA[C/T]TTTGACCAGAAAGGC	2177
rs748142616	snp	C/T	1.6483e-05	0.00287076	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098779	TGAGAGTGAGGATGA[C/T]ATGTCATCCCAGGCC	2177
rs748143287	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10066040	CTCAAAACTATTTTC[C/T]TAGTTCCCACAAGAC	2177
rs748156184	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10055988	GGTTCAAGCAGTTCT[C/G]TTGCCTCAGCCTCCT	2177
rs748171507	snp	A/C	3.31384e-05	0.00407039	missense	FANCD2	GRCh38.p7	3:10043505	AGGAAATCAAGAAAG[A/C]AGCGGTCAGAGCTGT	2177
rs748178251	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090223	AGCTACTTTTGGTTC[C/T]TGGTTCTTCCCAGGT	2177
rs748180733	snp	C/T	3.29603e-05	0.00405944	stop-gained	FANCD2	GRCh38.p7	3:10074590	TCCCATGCTTTTTTC[C/T]GAGAGCTGGACATTG	2177
rs748187375	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10068727	AACTGGAGGAATCGC[A/C]TTACCTGACTTCAAA	2177
rs748204365	in-del	-/AGTG	7.97273e-05	0.00631326	intron-variant	FANCD2	GRCh38.p7	3:10046727	GTTCATTACTTAGTA[-/AGTG]TCAGAGACTATTGAT	2177
rs748216345	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10089146	AAAAATTAGCCGGGC[A/G]TGGTGGCACATGCCT	2177
rs748232023	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097326	TTCCTCTTCCTAATA[A/G]GCCTGGGAGCGCTAT	2177
rs748282305	snp	G/T	1.67128e-05	0.00289069	missense	FANCD2	GRCh38.p7	3:10039333	CAGTCAACTAAAATG[G/T]CTTGACAGAGTTGTG	2177
rs748295839	snp	A/G	1.73462e-05	0.00294496	intron-variant	FANCD2	GRCh38.p7	3:10043201	TTCTGACATCCCACT[A/G]TCAGAGTTAGAGCTT	2177
rs748300590	snp	C/T	1.64955e-05	0.00287184	synonymous-codon	FANCD2	GRCh38.p7	3:10060329	AAGAAAGCAGCTCTC[C/T]AGCACCGTATTCAAG	2177
rs748312392	snp	A/G	6.68516e-05	0.00578112	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090283	ACGCATGCTTTTCCC[A/G]TCTTCTAGGCATACT	2177
rs748325682	in-del	-/C			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083013	GGTGGATCACTTGAG[-/C]CTCAGGAGTTCGAGA	2177
rs748327074	in-del	-/GTC	1.64732e-05	0.0028699	cds-indel	FANCD2	GRCh38.p7	3:10042585	GGTGATGGATAAGTT[-/GTC]GTCTATTAGATTGGA	2177
rs748337156	snp	C/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090506	GTTCTGTTGCCCAGA[C/G]TGGAGTGCAGTGGCA	2177
rs748387237	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10057105	AGGAGATCCACCCAC[C/T]TCTGCCTCCCAAAGT	2177
rs748421381	snp	C/T	1.64738e-05	0.00286995	intron-variant, missense	FANCD2, FANCD2OS	GRCh38.p7	3:10098892	GTTGGTGGAGCAGAA[C/T]TTTGCCTACTTATGT	2177
rs748423248	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10039091	CTTCTAGACATTTTT[C/G]TTAACATACGTAAGC	2177
rs748445025	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096156	CTTTGAATTCTTTAG[C/T]TGCCATTCTCTTTGG	2177
rs748468045	snp	C/T	1.64819e-05	0.00287066	synonymous-codon	FANCD2	GRCh38.p7	3:10063857	GGCCTCTGCACTTTA[C/T]TATGATGAATTTGCC	2177
rs748527843	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081946	AAATACTTTTGTTCC[C/T]CAGGGACAGGCGTTG	2177
rs748530086	snp	C/T	8.2689e-05	0.00642944	intron-variant	FANCD2	GRCh38.p7	3:10034425	TTTAGAGAAGGAAAA[C/T]TATGGTAGGAAACTG	2177
rs748542989	snp	A/T	1.64743e-05	0.00287	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087125	TTTGTTTTTCTTGTC[A/T]CCTTACAGCCAGAGC	2177
rs748559266	snp	C/G			missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090292	TTTCCCGTCTTCTAG[C/G]CATACTTTTGTTGTT	2177
rs748617351	in-del	-/TG			intron-variant	FANCD2	GRCh38.p7	3:10052536	ATTTTTTTTTTTTTG[-/TG]AGACAGAGTCTAGCT	2177
rs748630648	snp	C/T	1.64727e-05	0.00286986	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094311	GTCTCTTTGTGGAAG[C/T]ATTTCTGAAGCAATG	2177
rs748639181	snp	A/C			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082744	CCAGTTCTCTTCTAA[A/C]ACTCTGGTATCCGTT	2177
rs748651780	in-del	-/TA			intron-variant	FANCD2	GRCh38.p7	3:10055135	ATAAAACTACTTCAC[-/TA]TTTTATTTTATTTTT	2177
rs748662026	snp	C/T	1.64817e-05	0.00287064	intron-variant	FANCD2	GRCh38.p7	3:10063779	TTTAAACCATTCTTC[C/T]TCTTTGCTCCAGGTG	2177
rs748688174	snp	A/G	3.2981e-05	0.00406071	splice-donor-variant	FANCD2	GRCh38.p7	3:10052498	AGCAGCCACATCCAG[A/G]TAAGAGGCAATATGT	2177
rs748688910	snp	A/G	1.81985e-05	0.00301644	intron-variant	FANCD2	GRCh38.p7	3:10065988	CCGAGAGGTGAGCAG[A/G]GTTAATAGGATGTTT	2177
rs748710535	snp	A/G	3.29489e-05	0.00405874	intron-variant	FANCD2	GRCh38.p7	3:10078202	CCTTTCTCAAGGTTA[A/G]TGTAGGCAGAAGCAT	2177
rs748717972	snp	A/G	1.64874e-05	0.00287113	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085936	AGGTGAGTCATAACT[A/G]CATAGCCAAGATTGT	2177
rs748724233	snp	C/T	1.64787e-05	0.00287038	missense	FANCD2	GRCh38.p7	3:10041703	TTGACCCAAACTTCC[C/T]ATTGAAGGTAGAAAA	2177
rs748728765	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097650	ACACACATGCTGTAC[A/G]ATTTGTGTAGTTAAC	2177
rs748760473	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10029626	GGAACAGGTGGTGTT[C/T]GGTTACATAAATAAG	2177
rs748774754	snp	A/G	1.75231e-05	0.00295994	intron-variant	FANCD2	GRCh38.p7	3:10043892	TACTATGCATTTTCA[A/G]TATTGCAGACTTAAA	2177
rs748776499	in-del	-/GTATTCTACTTTGTTAATTAGTGGGTCAA	3.29522e-05	0.00405894	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088778	GAGGAATCTGTAGTT[lengthTooLong]GTATTCTACTTTGTT	2177
rs748781422	snp	C/T	1.66899e-05	0.00288871	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088566	TTTGGTTTCTTCCAA[C/T]GAGCCAAATAGCTTT	2177
rs748786895	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082956	AAGGGGCCTGACATC[A/G]TGGCTTATGCCTGTA	2177
rs748793722	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10045880	GCTGGGATTACAGGC[A/G]TGAGCCACCGTGCCT	2177
rs748816349	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10062025	CTTAATGCTAAATGA[C/T]GAGTTAATGGGTGCA	2177
rs748843683	in-del	-/AGGG	1.64756e-05	0.00287011	frameshift-variant, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085886	GTAGCCGACTGAAAC[-/AGGG]AGAACACAGCCAGCC	2177
rs748847222	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10064974	TCAAAAAAGTTTCTC[C/T]CGAGACAAATGGTAT	2177
rs748886093	snp	C/T	1.65578e-05	0.00287726	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081074	ATCCAGCAGTTTCTT[C/T]ACTCATAACTCTGCA	2177
rs748907382	snp	G/T			downstream-variant-500B, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10102301	GGCACACGCCACCAT[G/T]CCTGGCTAATCTTTG	2177
rs748941966	snp	A/G	8.23635e-05	0.00641677	intron-variant	FANCD2	GRCh38.p7	3:10064725	TTCTGGTTTTTCTCC[A/G]CAGTGACTTTCCATT	2177
rs748957220	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10047430	GCTATGTTTATTAAC[C/T]GGTTATTTAGTCTGG	2177
rs748972027	snp	C/T	1.64741e-05	0.00286998	intron-variant	FANCD2	GRCh38.p7	3:10042675	TGAGGTATGCTCTTA[C/T]ATCCCATCACACCTA	2177
rs748995059	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100593	GCCGGGCTGGTCTCG[A/G]ACTCCTAACCTCAGA	2177
rs749023278	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10076713	CCCCACTACACCCGG[C/T]TAGTTTTTTTATTTG	2177
rs749039770	snp	A/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088720	GGTTCTGTTTTATAC[A/T]GTTAGCTAACTGCTT	2177
rs749060270	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10035158	GTGGAAAACAGATTT[C/G]TTTTTTTTTTACAGT	2177
rs749082091	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10038899	GCTTGCCTTTTTAAG[A/C]ACTTACTGCGTTGAT	2177
rs749094775	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090148	TACTGAGTCCTTTCC[A/G]CTCCCCCATCCTCTT	2177
rs749133639	snp	C/T	1.65031e-05	0.00287251	missense	FANCD2	GRCh38.p7	3:10043086	AAGTTGGATCTGCAG[C/T]ATTGTGTTTTGCCAT	2177
rs749139424	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10037850	TTTGCAATAAGTAGT[G/T]CAGTATTTTGTTTAA	2177
rs749142910	snp	A/T	0.00011726	0.00765612	intron-variant	FANCD2	GRCh38.p7	3:10032785	GGTTTAAGTTTTAAT[A/T]TTTCCTTTACTATTT	2177
rs749176909	in-del	-/TT	1.65233e-05	0.00287426	intron-variant	FANCD2	GRCh38.p7	3:10034452	ACTGGTGACCAGCTC[-/TT]CTTTTTTCTGCATAG	2177
rs749194816	in-del	-/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097398	GAGACAGGTACACCC[-/G]GGGGGGGCCCAGTTC	2177
rs749208049	snp	C/T	3.2956e-05	0.00405918	synonymous-codon	FANCD2	GRCh38.p7	3:10047922	CCCACTCAAGGTTCT[C/T]AAGGATATGTGTTCA	2177
rs749216958	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086161	ATAAACTCAGCCTTT[C/T]CAAGTAATAATGATG	2177
rs749244864	snp	A/G			upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025256	CCACCACGCCTGGCT[A/G]TGAACAAGTTTTTTG	2177
rs749246462	snp	C/T	1.65272e-05	0.0028746	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096311	AAAAGATGGATGTTA[C/T]TTATTTCCATTCAGA	2177
rs749247027	snp	A/G	2.5265e-05	0.00355413	intron-variant	FANCD2	GRCh38.p7	3:10067364	CTAGGCCAGTAGTGA[A/G]GCAATAAAGCACTTA	2177
rs749256664	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10062799	CAAGCAATTCTCCTG[C/T]CTCAGCCTCCCAAGT	2177
rs749286455	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10077565	GTCTCAAAAAAAAAA[A/T]TTTTTTTTCACCCAT	2177
rs749325183	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10068019	GGGTATAGATCCATA[A/G]CTACTATTAAACTGA	2177
rs749388615	in-del	-/C			intron-variant	FANCD2	GRCh38.p7	3:10047272	TTTCTGTGTTTATTT[-/C]TGCCAATTATACATG	2177
rs749394475	snp	C/T	1.64738e-05	0.00286995	intron-variant, synonymous-codon	FANCD2, FANCD2OS	GRCh38.p7	3:10098905	AACTTTGCCTACTTA[C/T]GTTTATTGTCAAATG	2177
rs749397374	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10029090	GATCTAGACACATGC[C/T]ATGTTAGTGATGTGA	2177
rs749402179	snp	C/G	1.64833e-05	0.00287078	missense	FANCD2	GRCh38.p7	3:10028702	TGAGGATAAAGAGAG[C/G]CTGACAGAAGATGCC	2177
rs749409677	snp	A/G	9.26913e-05	0.00680713	intron-variant	FANCD2	GRCh38.p7	3:10046755	ATTGATTTTTAATCT[A/G]AAACAGAAAGCTTTA	2177
rs749410557	snp	C/T	1.64746e-05	0.00287002	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092196	ATTCATGAAGAGAAA[C/T]TCCTCTACTGGAACA	2177
rs749465456	snp	A/C	1.6473e-05	0.00286988	missense, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10081425	TAATGTCTTCCTGCT[A/C]TCAGAGGCTGCTGCA	2177
rs749470358	snp	C/G			utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101680	GAGCCACCGCTCCCA[C/G]CCATATTTTGTTCTT	2177
rs749474035	snp	G/T	1.64741e-05	0.00286998	intron-variant	FANCD2	GRCh38.p7	3:10065377	GTGTGGTCTAGAAAT[G/T]TATTTCTCCTTCTCA	2177
rs749480680	in-del	-/TT	0.00574209	0.0532736	intron-variant	FANCD2	GRCh38.p7	3:10052523	ATATGTTGGGAAAGA[-/TT]TTTTTTTTTTTGAGA	2177
rs749495188	snp	A/G	1.6768e-05	0.00289546	intron-variant	FANCD2	GRCh38.p7	3:10043628	ATTATCAAGGAGGAA[A/G]TGAGTGGCAATTAGT	2177
rs749502961	snp	C/T	1.73516e-05	0.00294542	intron-variant	FANCD2	GRCh38.p7	3:10039377	GCTTATGGACTTTAT[C/T]TCTTGAATTTAAAGA	2177
rs749593133	snp	A/C	1.6476e-05	0.00287014	missense	FANCD2	GRCh38.p7	3:10039723	TCTTCTACTGCAGGA[A/C]CTCACCACCAAGATC	2177
rs749606134	snp	C/G	1.64727e-05	0.00286986	missense	FANCD2	GRCh38.p7	3:10049392	GTGGTTGGTGCCTTA[C/G]TGACCCATATCTGCA	2177
rs749628499	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094018	GCTCCCCTCTACTCT[A/G]TGCTCTCACTCCTAA	2177
rs749629210	snp	C/T	1.8086e-05	0.0030071	intron-variant	FANCD2	GRCh38.p7	3:10074506	GATTTATATATTCTC[C/T]TTGTTGCTGTGACTT	2177
rs749651234	snp	A/G	6.97484e-05	0.00590503	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095149	GGGTATCTTGAATCT[A/G]AAATGAAATCAGGAC	2177
rs749662817	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10041990	TGCAACCTCTACCTA[C/G]CAAGTTCAAGCAGTT	2177
rs749670036	snp	A/T	3.29527e-05	0.00405898	synonymous-codon	FANCD2	GRCh38.p7	3:10074616	CATTGAGGTCTTCTC[A/T]ATTCTACATTGTGGA	2177
rs749682242	in-del	-/ACAGAA	4.95769e-05	0.00497856	intron-variant	FANCD2	GRCh38.p7	3:10048087	TGGCAAGGAGGGAAC[-/ACAGAA]AGGGAAAATAATCTG	2177
rs749698541	snp	A/G	1.65578e-05	0.00287726	missense	FANCD2	GRCh38.p7	3:10043513	AAGAAAGCAGCGGTC[A/G]GAGCTGTATTATTCT	2177
rs749722893	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10058706	TTTCATTGGTCTATA[C/T]GTCTGTCCTTCTGCC	2177
rs749754982	snp	G/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094975	ATGTAAAACTAAAAT[G/T]CAGGTCTTATAACTC	2177
rs749767303	snp	A/G	3.30628e-05	0.00406575	intron-variant	FANCD2	GRCh38.p7	3:10034441	TATGGTAGGAAACTG[A/G]TGACCAGCTCTTCTT	2177
rs749776442	snp	A/G			missense	FANCD2	GRCh38.p7	3:10042646	CTTCATTCCGTAACA[A/G]CCATGGATACACTTG	2177
rs749797517	snp	C/T	3.29843e-05	0.00406092	intron-variant	FANCD2	GRCh38.p7	3:10063926	GGTAAAGCCAATTGT[C/T]TTTTCTTAAAGCAAT	2177
rs749826479	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10078544	TATTTTTTGTAGAGA[C/G]GGGGTTTCACCGTGT	2177
rs749849880	snp	C/T	3.30256e-05	0.00406346	intron-variant	FANCD2	GRCh38.p7	3:10034550	AAGTATGTATTTTTC[C/T]CCTGGTATTTTTGCT	2177
rs749868748	snp	C/G	3.32375e-05	0.00407647	missense	FANCD2	GRCh38.p7	3:10049494	ATGATGATGAATGCT[C/G]TCTTTGTAAAGGTAT	2177
rs749888624	snp	A/T	1.66496e-05	0.00288522	splice-donor-variant	FANCD2	GRCh38.p7	3:10060405	ATGGCGGCAGACAGG[A/T]ACACGTGGAGATTCT	2177
rs749891839	snp	G/T	1.68411e-05	0.00290177	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090266	TGCATCATGGTGTGG[G/T]CACGCATGCTTTTCC	2177
rs749930493	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10077485	GCTTGAACCTGGGAC[A/G]CAGAGGTTGTAGTGA	2177
rs749940072	snp	A/G	3.29544e-05	0.00405908	intron-variant, synonymous-codon	FANCD2, FANCD2OS	GRCh38.p7	3:10098947	ATTTCCATTCCCTCC[A/G]TAACAGCTTCTGTGC	2177
rs749974836	snp	A/G			synonymous-codon	FANCD2	GRCh38.p7	3:10046723	CTCTGTTCATTACTT[A/G]GTAAGTGTCAGAGAC	2177
rs749978500	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10062124	TAAAGTATAATAATA[A/C]TTTAAAAAAAAATTC	2177
rs750030381	snp	A/G	1.64727e-05	0.00286986	missense, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10081368	CTGCTGAGAATCACG[A/G]TGTAGTTGATGGACC	2177
rs750053115	snp	G/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10089149	AATTAGCCGGGCGTG[G/T]TGGCACATGCCTGTA	2177
rs750058299	snp	A/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095360	ATGGGCTACCATCCT[A/T]CTTCCTTTATATCTG	2177
rs750088699	snp	A/C	1.6691e-05	0.00288881	intron-variant	FANCD2	GRCh38.p7	3:10064923	GTGTTTTGAATGTTC[A/C]TGGGGAATTCCACAG	2177
rs750123175	snp	C/G/T	3.29594e-05	0.00405941	intron-variant	FANCD2	GRCh38.p7	3:10039682	TCTTTCTTTATTCTG[C/G/T]GTAATGTGCTGCAGT	2177
rs750130327	snp	A/G	0.000133663	0.00817396	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090343	TGAACTAGAGAAGAC[A/G]GTGAAAAAAATTGAG	2177
rs750159182	in-del	-/ATT	1.65842e-05	0.00287955	intron-variant	FANCD2	GRCh38.p7	3:10052362	TTAGCTGCTAGCCTC[-/ATT]GTTGGCATCATTTTT	2177
rs750160682	snp	C/G			intron-variant, utr-variant-5-prime, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026553	GTCCGGGCCGCGGTC[C/G]GCGTTCTCCTCTGGG	2177
rs750174394	in-del	-/GTTA			intron-variant	FANCD2	GRCh38.p7	3:10072622	AGTTTTTTTCTGTTT[-/GTTA]GTTATATATCATTAT	2177
rs750183272	snp	C/T	1.65051e-05	0.00287267	intron-variant	FANCD2	GRCh38.p7	3:10073392	GGTATCCGTGAAGGT[C/T]TGTGACATCCCAGTG	2177
rs750190302	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10031812	GTCCCATTCCCAAGA[G/T]TTTGACTCAGTAACT	2177
rs750228398	snp	A/G	1.64746e-05	0.00287002	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087090	ATATATCTGTGACAC[A/G]TAGGATACTATTGCA	2177
rs750235266	snp	A/C	0.000200003	0.00999808	intron-variant	FANCD2	GRCh38.p7	3:10043474	TTTTTTTCCTCTCTG[A/C]TACTTGTAGTTCCTC	2177
rs750254657	snp	C/T	1.85266e-05	0.00304351	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098689	ATGTGATCATTATAA[C/T]CCACCATTTTCTTGG	2177
rs750261535	snp	C/T	1.64735e-05	0.00286993	intron-variant, synonymous-codon	FANCD2, FANCD2OS	GRCh38.p7	3:10098845	CCCACCAGAGTCTGG[C/T]ACTGATGGTTGCATT	2177
rs750310406	snp	A/G	3.29723e-05	0.00406018	intron-variant	FANCD2	GRCh38.p7	3:10048064	CAGGTATGTTGAAAC[A/G]TTTATTTTGGCAAGG	2177
rs750336008	snp	A/G	1.67156e-05	0.00289093	intron-variant	FANCD2	GRCh38.p7	3:10033001	CTAATTTTATTCTCT[A/G]GGTTTAATGAAATAG	2177
rs750338758	in-del	-/G	0.0672347	0.170578	splice-donor-variant	FANCD2	GRCh38.p7	3:10046724	TCTGTTCATTACTTA[-/G]TAAGTGTCAGAGACT	2177
rs750346438	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10056926	GTGGTGTTATCTTGG[C/T]TTACTGCAACCTCCA	2177
rs750353000	snp	A/G	1.64819e-05	0.00287066	missense	FANCD2	GRCh38.p7	3:10063886	CCAACCTGATCCAAC[A/G]TGAAAAGCTGGATCC	2177
rs750409411	snp	A/G	3.29473e-05	0.00405864	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087187	TTCCCAGTTTCCAGT[A/G]TGCTCTTTATCTCAT	2177
rs750435620	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10051601	CAATGTCGAGAAGCA[G/T]CAAGGAGGAGAGAAT	2177
rs750445060	snp	C/T	1.68352e-05	0.00290126	intron-variant	FANCD2	GRCh38.p7	3:10049340	GCCATCCATATTTTG[C/T]TTTACACTGTTCTGT	2177
rs750459687	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10061577	AGGATTTACCTCATA[C/G]AGTCATTGAGAACAT	2177
rs750465384	in-del	-/AG			intron-variant	FANCD2	GRCh38.p7	3:10069406	ACATCACTGAGCCTC[-/AG]AGAAATGCAAATCAA	2177
rs750473069	snp	A/G	1.67607e-05	0.00289483	missense	FANCD2	GRCh38.p7	3:10065959	TCTCTCATATTTCTT[A/G]CTCTCAACTGGTTCC	2177
rs750490552	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094722	AAAAAAAAAAAAGCT[C/T]ATTTGTGTCATAAAA	2177
rs750501988	snp	A/G	3.29625e-05	0.00405958	synonymous-codon	FANCD2	GRCh38.p7	3:10063830	TCATTCCTGCAGTGA[A/G]CAGTCTCCTCAGGCC	2177
rs750519670	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10070594	TGGGAAGTGAGGAGC[C/T]CCTCTGCCCGGCCAC	2177
rs750534583	snp	A/T	8.26398e-05	0.00642753	missense	FANCD2	GRCh38.p7	3:10032911	AAATGACAGCATCTT[A/T]GTAAAGCTTCTTAAG	2177
rs750558317	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10060077	GAGGCTGAGGCAGGA[G/T]AATCGTTTGAACCTG	2177
rs750559078	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10075847	ACCATTATCCTGCCT[C/T]AGCCTCCCAAGTAGC	2177
rs750567765	in-del	-/C	1.68742e-05	0.00290462	intron-variant	FANCD2	GRCh38.p7	3:10074519	TCTTTGTTGCTGTGA[-/C]TTCCCCATAGGAGTT	2177
rs750588337	snp	A/G	1.64743e-05	0.00287	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094244	CTCAGGGGCCTTTCA[A/G]TGAGATACCTCAGCT	2177
rs750601467	in-del	-/T			intron-variant	FANCD2	GRCh38.p7	3:10031001	GAAACTGAAGAGGAA[-/T]TAATATAGGAAATTA	2177
rs750629741	snp	A/T	3.32923e-05	0.00407983	intron-variant	FANCD2	GRCh38.p7	3:10046559	ACTGTTTTTCTGTTG[A/T]TGCATATTTATTGAC	2177
rs750650450	snp	A/G			intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10081479	GGTAAGTATGTGGGA[A/G]GTGTGGAGAGAACTG	2177
rs750675776	snp	A/G	1.65247e-05	0.00287438	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093240	AGGCTGGAGTGCTCA[A/G]AGGAGCAGATCTCAG	2177
rs750713448	snp	A/G	0.000811359	0.0201251	intron-variant	FANCD2	GRCh38.p7	3:10040507	TCATTTGTGGAGCCT[A/G]TTAAACATCTACCTT	2177
rs750767750	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10051945	AAGCTGGGAAGGGAT[A/G]ATATGGCAAGGAATA	2177
rs750770422	in-del	-/CT			intron-variant	FANCD2	GRCh38.p7	3:10079235	GGCATTAGAACAAGA[-/CT]CTGTCTCAGAAATAA	2177
rs750812519	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086992	GCTTGAAGAGGGTTG[C/T]TACTAAAGCACCTGA	2177
rs750812811	snp	A/C	1.64855e-05	0.00287097	missense	FANCD2	GRCh38.p7	3:10052465	AGCACACTGGCATTT[A/C]GCAAACAGAATGAAG	2177
rs750828943	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085597	GGATTTCACCGTGTT[A/G]GCCAAGATGGTCTCC	2177
rs750865745	snp	C/G	1.64735e-05	0.00286993	missense	FANCD2	GRCh38.p7	3:10078159	AAGCTGGAGAGTATG[C/G]TGACACCTCCTATTG	2177
rs750883248	snp	G/T	4.54969e-05	0.00476932	intron-variant	FANCD2	GRCh38.p7	3:10073026	GTCTCTAAATAAGCT[G/T]CATTGAATTAACCTA	2177
rs750892839	snp	G/T	1.64741e-05	0.00286998	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088803	TTTGTTAATTAGTGG[G/T]TCAAATATTTGACTC	2177
rs750897102	in-del	-/CTT			intron-variant	FANCD2	GRCh38.p7	3:10041842	ACATTTGATATCTCT[-/CTT]TTTTTTTTTTTTTCC	2177
rs750939264	snp	A/T	1.64784e-05	0.00287035	intron-variant	FANCD2	GRCh38.p7	3:10035275	ATTTGATGGAAGAGG[A/T]TTGTGGTGTATGCTC	2177
rs750976498	snp	C/T	1.87026e-05	0.00305793	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098686	TAAATGTGATCATTA[C/T]AACCCACCATTTTCT	2177
rs751013429	snp	G/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088073	CTATTGATTAAAAGG[G/T]GAAGGTTTGGTCTCA	2177
rs751015600	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10074850	GTGTTTGTAAGTCAT[A/C]AGGTTTGTAATAATG	2177
rs751021211	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10045215	ACTCTGTCACCTAGG[A/C]TGGACTGCACTGGCG	2177
rs751027444	snp	A/T	0.000115305	0.00759205	missense, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10081389	TTGATGGACCAGGAG[A/T]GAAAGTTCAGGAGTA	2177
rs751065357	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10055355	CCCCTAATAATCACT[A/G]ATCACATTCTGTCTA	2177
rs751107447	snp	C/T	1.64735e-05	0.00286993	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092161	TGACTCAGAGGTGCC[C/T]ATATATTTGGCTGCC	2177
rs751122580	snp	C/T	1.65269e-05	0.00287457	missense	FANCD2	GRCh38.p7	3:10072877	TTGTTTCAGTCACCC[C/T]AGACTATGTCCCTCC	2177
rs751126921	snp	C/T	1.64743e-05	0.00287	missense	FANCD2	GRCh38.p7	3:10039755	TGCAGCTGATCAGTA[C/T]TGCTCCAGAGAACCT	2177
rs751127451	snp	C/T	1.64735e-05	0.00286993	missense	FANCD2	GRCh38.p7	3:10042641	TCATTCTTCATTCCG[C/T]AACAGCCATGGATAC	2177
rs751154253	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10069005	AAATGGATTATAGAC[G/T]TAAATCTAAGACTTC	2177
rs751157372	snp	A/G/T	4.964e-05	0.00498176	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096285	ATGTGAAGGCATGAT[A/G/T]ATAAACTCACAAAAG	2177
rs751160740	snp	A/G			upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025103	GGACTACAGGCACAC[A/G]CCACTGCACCTGGCT	2177
rs751173245	snp	A/T	1.64746e-05	0.00287002	missense	FANCD2	GRCh38.p7	3:10039781	AACCTGCAGCATGAC[A/T]TCATCACCAGCCTAC	2177
rs751175161	snp	C/T	0.000131852	0.00811842	synonymous-codon	FANCD2	GRCh38.p7	3:10028676	GTTTCCAAAAGAAGA[C/T]TGTCAAAATCTGAGG	2177
rs751226705	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10038422	AGATGGAAGTGGTCC[A/C]AAACTTTAGATATAG	2177
rs751263095	snp	C/G	1.66012e-05	0.00288103	intron-variant	FANCD2	GRCh38.p7	3:10028770	GTAGCAATGTGTGAG[C/G]CATGTGAGAGATATA	2177
rs751273814	snp	A/G	1.64803e-05	0.00287052	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10081500	GAGAGAACTGAGTAT[A/G]TACTTGCTTTTATTT	2177
rs751294144	snp	A/G/T	2.07205e-05	0.00321866	intron-variant	FANCD2	GRCh38.p7	3:10062260	GTCTTTTTTTTTTTT[A/G/T]TAGAGAGTCTCGCTC	2177
rs751299928	snp	C/T	4.94482e-05	0.00497209	synonymous-codon	FANCD2	GRCh38.p7	3:10074670	TACTGAAATGCACAC[C/T]GAAGTAAGTGACAGG	2177
rs751312398	snp	C/T	1.64836e-05	0.0028708	intron-variant	FANCD2	GRCh38.p7	3:10065352	GTACGTGGAGTAATA[C/T]ACCTATGAAGTGTGG	2177
rs751316796	in-del	-/T			intron-variant	FANCD2	GRCh38.p7	3:10069490	CTCCCCCTCCCCCTC[-/T]CCCGTCTCCCTCTGA	2177
rs751345893	snp	C/G	1.64727e-05	0.00286986	synonymous-codon	FANCD2	GRCh38.p7	3:10065415	GTCTCCGCTGTGCCT[C/G]GCTCCGTATTTCCGG	2177
rs751384092	snp	A/C			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094633	GTGCTACTGCACTCT[A/C]AGGTCCTCATGTATC	2177
rs751393709	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10030925	AGGAAGTTGTGAAGC[G/T]CCAATGGTTGATTAG	2177
rs751421626	snp	A/G/T	3.31434e-05	0.00407073	missense	FANCD2	GRCh38.p7	3:10043503	TCAGGAAATCAAGAA[A/G/T]GCAGCGGTCAGAGCT	2177
rs751474920	in-del	-/TTT	0.000720721	0.0189695	intron-variant	FANCD2	GRCh38.p7	3:10062248	TTTCTTTTTCCTGTC[-/TTT]TTTTTTTTTTTAGAG	2177
rs751481349	snp	C/T	1.66043e-05	0.00288129	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101165	AACCTAAAATGCTTA[C/T]TTATTTATTCTTTGC	2177
rs751484412	snp	C/T	1.65685e-05	0.00287819	missense	FANCD2	GRCh38.p7	3:10049459	TCCTTCTAGAGTTGG[C/T]AGTGTTAAACCCATC	2177
rs751496034	snp	C/T	1.6489e-05	0.00287128	missense	FANCD2	GRCh38.p7	3:10074567	AGACATCATTGTTAC[C/T]ACATAATTCCCATGC	2177
rs751527593	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10074753	ATTTCACAAAGAACA[C/T]TGTGACACTGAGGAG	2177
rs751563131	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10067879	GATTGTTCAACATAT[A/G]TAAATCAATGTGATA	2177
rs751572704	snp	A/G	1.65523e-05	0.00287678	missense	FANCD2	GRCh38.p7	3:10043572	AGATATGAGAAAACC[A/G]TTTCAGAAGCCTGGA	2177
rs751581738	snp	G/T	1.64947e-05	0.00287177	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10098975	TGCTTATATAATTTT[G/T]GGGACCCAGAAGAAA	2177
rs751596355	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082345	CCAGACTCCCATTAT[C/T]TCTCAACCTGGACTG	2177
rs751616030	snp	C/T	3.31011e-05	0.0040681	intron-variant	FANCD2	GRCh38.p7	3:10049355	TTTTACACTGTTCTG[C/T]TGACTCTCCCCTGTA	2177
rs751626782	snp	A/G	1.64817e-05	0.00287064	missense	FANCD2	GRCh38.p7	3:10063898	AACATGAAAAGCTGG[A/G]TCCAAAAGCCCTGGT	2177
rs751633764	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10058319	CATCGCTGGCACCAC[A/G]AAGGTTGCCACTCCA	2177
rs751645479	in-del	-/TT			intron-variant	FANCD2	GRCh38.p7	3:10033696	GCTATCAAAGCTAAG[-/TT]TCTTTTTTTTTTTTT	2177
rs751714676	snp	A/G	1.65712e-05	0.00287843	intron-variant	FANCD2	GRCh38.p7	3:10064313	TAGGGCTGTACAGCA[A/G]GTACACTCTGCACTG	2177
rs751727264	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10037328	CACAGTAAAATAAAT[A/G]CATTTTTTCCTACTC	2177
rs751739571	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10042354	TGTTTCACATTTATT[A/G]CCCGTCTATTTTTGA	2177
rs751747933	snp	A/G	4.9561e-05	0.00497775	missense	FANCD2	GRCh38.p7	3:10046700	GAACAGCTGCTCCAG[A/G]GTACATTCTCTGTTC	2177
rs751756098	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10077833	CCAGGAGTTTGAGAC[C/T]AGCTTGGGCAATATA	2177
rs751769229	snp	A/C	1.64819e-05	0.00287066	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094388	AAGAGCAGAGAACAA[A/C]GATATGCACTGAAGA	2177
rs751774917	snp	C/G	1.64757e-05	0.00287012	missense	FANCD2	GRCh38.p7	3:10041687	CTTTCAAGCCTCCGA[C/G]TTGACCCAAACTTCC	2177
rs751802397	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10061168	CTTCGGCATACAGCA[C/T]ACATCATAAATACTA	2177
rs751819584	snp	C/G	1.64751e-05	0.00287007	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087098	GTGACACATAGGATA[C/G]TATTGCATTTGTTTG	2177
rs751864173	snp	C/T	1.64735e-05	0.00286993	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088831	CTCTCAATGCAGTAT[C/T]TACCTGGAGCACACA	2177
rs751881206	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088293	CCAGTGGATCAGGAA[C/T]GTGACAGCTTTTTGT	2177
rs751895071	in-del	-/TA	1.64779e-05	0.00287031	frameshift-variant	FANCD2	GRCh38.p7	3:10074616	CATTGAGGTCTTCTC[-/TA]TTCTACATTGTGGAC	2177
rs751909526	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10066608	TTAAAGACTCAGCCA[A/G]GGTCACACAGTAAGT	2177
rs751942254	snp	A/G	1.64746e-05	0.00287002	missense	FANCD2	GRCh38.p7	3:10046640	CAGACAAAGAAGTAC[A/G]TTGACAGGGTGCTAA	2177
rs751963392	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098662	ACTCAACCTTCTCCC[C/T]TATTACCCTAAATGT	2177
rs751981960	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097405	GGTACACCCGGGGGG[A/G]CCCAGTTCAGAGACC	2177
rs751993012	snp	C/T	3.29468e-05	0.00405861	missense	FANCD2	GRCh38.p7	3:10064779	TGGAAGAATACGACA[C/T]TCAGGATGGGATTGC	2177
rs752013429	snp	C/G	1.70956e-05	0.00292361	missense	FANCD2	GRCh38.p7	3:10065970	TCTTACTCTCAACTG[C/G]TTCCGAGAGGTGAGC	2177
rs752015292	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10033378	TGCACTCCAGCCTGG[A/G]CGACAAGAGTGAGAC	2177
rs752040755	snp	A/C	3.30033e-05	0.00406209	missense	FANCD2	GRCh38.p7	3:10052483	AAACAGAATGAAGCC[A/C]GCAGCCACATCCAGG	2177
rs752053879	snp	A/G	3.31362e-05	0.00407026	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081056	CTTAGTTTCTGAGAC[A/G]CTATCCAGCAGTTTC	2177
rs752060491	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10035753	TAAACTCTTCCTTTT[A/C]ACTGGAAATCTTGAA	2177
rs752062671	snp	A/G	3.29598e-05	0.00405941	missense, downstream-variant-500B	FANCD2, FANCD2OS	GRCh38.p7	3:10081164	CCCAAGAAATTGTTC[A/G]TTGTGTTTTTCAACT	2177
rs752093385	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10063074	AAGAAAGATATGCCA[G/T]GTTTATGGAATAACA	2177
rs752126828	snp	C/T	3.31824e-05	0.00407309	intron-variant	FANCD2	GRCh38.p7	3:10046566	TTCTGTTGTTGCATA[C/T]TTATTGACAATAGGT	2177
rs752148524	snp	G/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085263	AGAAAGAGGAAAGAA[G/T]AAAAGAAACCTATGA	2177
rs752152872	snp	A/T	1.6477e-05	0.00287024	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088997	TAAGATAGAATCATC[A/T]TCAGGCTGGGCACGG	2177
rs752180124	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087996	TCTTAGAATGCAGCT[C/T]ATCCTAGTTGGCAGC	2177
rs752181826	in-del	-/GTCATCC	1.69775e-05	0.0029135	intron-variant	FANCD2	GRCh38.p7	3:10043186	AGGATGTCACAATTT[-/GTCATCC]TCTGACATCCCACTG	2177
rs752187357	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10069191	CCTTTCCTCTGCATA[G/T]CAAAGGAAACACCAA	2177
rs752193273	snp	A/G/T			intron-variant	FANCD2	GRCh38.p7	3:10066780	CCCAGGCTGGAGTGC[A/G/T]GTGGCTCAATCTCGG	2177
rs752236696	snp	A/G			intron-variant, downstream-variant-500B	FANCD2, FANCD2OS	GRCh38.p7	3:10099753	ACAGAGTGAGACTCC[A/G]TCTCAACAACAACAA	2177
rs752246063	snp	A/G	1.65282e-05	0.00287469	missense	FANCD2	GRCh38.p7	3:10032898	ATGAAGTTGAAGAAA[A/G]TGACAGCATCTTTGT	2177
rs752256004	snp	A/G	1.64751e-05	0.00287007	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085874	TCCATGTCCTTAGTA[A/G]CCGACTGAAACAGGG	2177
rs752267036	snp	G/T	1.6636e-05	0.00288405	missense	FANCD2	GRCh38.p7	3:10043150	GTAAAGGACGAGCAA[G/T]GTAAAGAGCTCATCC	2177
rs752268889	snp	A/C	8.23662e-05	0.00641688	synonymous-codon	FANCD2	GRCh38.p7	3:10047976	TTTGCTTCACTCTCT[A/C]GACCAGAGTATAATT	2177
rs752277320	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095462	TAGAGGGGAATCTCC[A/G]CATCTGAAATTTGAT	2177
rs752284159	snp	C/T	1.82221e-05	0.00301839	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098693	GATCATTATAACCCA[C/T]CATTTTCTTGGTCCA	2177
rs752289374	snp	C/T	1.65048e-05	0.00287265	missense	FANCD2	GRCh38.p7	3:10072888	ACCCCAGACTATGTC[C/T]CTCCTCTTGGAAACT	2177
rs752304714	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10037345	ATTTTTTCCTACTCT[C/G]AAAGGGTCTCCTTGT	2177
rs752328242	in-del	-/TCAAAGTACCC	1.65792e-05	0.00287912	intron-variant	FANCD2	GRCh38.p7	3:10036364	GTTATTATGGAATGT[-/TCAAAGTACCC]TGATGTACTTAAGTT	2177
rs752360517	snp	A/T	8.25648e-05	0.00642461	synonymous-codon	FANCD2	GRCh38.p7	3:10043064	GGTAATTTCTGAGCT[A/T]CGGGAGAAGTTGGAT	2177
rs752376206	snp	G/T	1.64738e-05	0.00286995	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096424	GCTCACTCTCAACAA[G/T]TGTAGAGAGGCTTTC	2177
rs752401644	in-del	-/G	5.06269e-05	0.00503099	intron-variant	FANCD2	GRCh38.p7	3:10043173	GCTCATCCTCACACA[-/G]GATGTCACAATTTTC	2177
rs752459505	snp	C/G	1.64757e-05	0.00287012	missense	FANCD2	GRCh38.p7	3:10048036	ATTTAAGTTTTTTGA[C/G]ACGTACTGCCAGCAG	2177
rs752477548	snp	A/C	4.08438e-05	0.00451888	intron-variant	FANCD2	GRCh38.p7	3:10062139	ATTTAAAAAAAAATT[A/C]TTTGTTTTTAGAAGT	2177
rs752520384	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10041222	AAACAAACAAAAAAA[A/G]AAGCAATCTATCACT	2177
rs752524190	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10030029	TGACCTCAAGTGATC[C/T]ATCCATCTCGGCCTC	2177
rs752525444	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10058204	GAGATTAGGCCCACT[C/T]TTGTGCTTGTCTCCC	2177
rs752545236	snp	C/T	0.00103788	0.0227566	intron-variant	FANCD2	GRCh38.p7	3:10032263	TCTGTGGGTTATTCT[C/T]GTTAGGCACTTATTT	2177
rs752550362	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092555	ATGATCTGAGCGCAC[A/G]TTCCCTCTTCTAACC	2177
rs752567443	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10050715	CAAATGTCCATAGAA[A/G]GAAAATGAGAAACCT	2177
rs752581355	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10042247	AATCTTCCATGTTGT[C/G]TGAGTCATACCTGCT	2177
rs752621186	snp	C/T	3.29451e-05	0.00405851	missense	FANCD2	GRCh38.p7	3:10065428	CTGGCTCCGTATTTC[C/T]GGTTACTGAGACTTT	2177
rs752630007	snp	C/T	4.95184e-05	0.00497562	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092276	GGAGACTGCTTGACA[C/T]ATCTCACCAAATAAC	2177
rs752630158	snp	G/T	1.64822e-05	0.00287068	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10081509	GAGTATATACTTGCT[G/T]TTATTTGACAGTCAC	2177
rs752725991	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10080159	ACCTCATGATCCACC[C/T]GCCTTGGCCTCCCAA	2177
rs752741393	snp	A/C/G	4.9429e-05	0.00497116	missense	FANCD2	GRCh38.p7	3:10039823	GGGGATTCCCAGCAC[A/C/G]CTGATGTGGGGAAAG	2177
rs752763591	snp	G/T	4.94809e-05	0.00497373	intron-variant	FANCD2	GRCh38.p7	3:10074687	AAGTAAGTGACAGGC[G/T]AGGATCTCAGAATTT	2177
rs752791782	snp	C/T	1.65053e-05	0.0028727	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10098981	TATAATTTTTGGGAC[C/T]CAGAAGAAACAACGA	2177
rs752799639	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10033029	TAGTTCAGGACTGAA[G/T]CATGGGTTTTCTAAA	2177
rs752815037	snp	A/G	3.295e-05	0.00405881	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087219	AGACTTTTGATGGTT[A/G]TTTTGGAGAAATCAA	2177
rs752837688	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084033	GAGTCTCACTCTGTC[A/G]CTCAGGCTGGAGTGC	2177
rs752879499	in-del	-/T	0.0126393	0.078485	intron-variant	FANCD2	GRCh38.p7	3:10052523	ATATGTTGGGAAAGA[-/T]TTTTTTTTTTTTGAG	2177
rs752880741	snp	A/C	1.65012e-05	0.00287234	missense	FANCD2	GRCh38.p7	3:10034534	CACCCTTCCTATCCC[A/C]AAGTATGTATTTTTC	2177
rs752880854	snp	C/G	3.29468e-05	0.00405861	missense	FANCD2	GRCh38.p7	3:10042611	GATTGGAGGATTTAC[C/G]TGTGATAATAAAGTT	2177
rs752886865	snp	A/G			utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101409	TTTTTTTTTAAAGAC[A/G]GGGACTCGCTGTGTT	2177
rs752947607	snp	C/G	1.65359e-05	0.00287536	intron-variant	FANCD2	GRCh38.p7	3:10064326	CAAGTACACTCTGCA[C/G]TGCCCTTTTTGTTTG	2177
rs753028953	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10077283	TTTACCCTGCTGGGC[A/G]CAGTGGCTCACGCCT	2177
rs753041155	snp	C/G	3.29647e-05	0.00405971	synonymous-codon	FANCD2	GRCh38.p7	3:10063911	GGATCCAAAAGCCCT[C/G]GTAAAGCCAATTGTC	2177
rs753058956	snp	A/G	1.64825e-05	0.00287071	synonymous-codon, downstream-variant-500B	FANCD2, FANCD2OS	GRCh38.p7	3:10081180	TTGTGTTTTTCAACT[A/G]CTGACCCCAATGTGT	2177
rs753077060	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10042531	GTGACATGAAAACCT[A/G]TTAAGTTTCTGTGCT	2177
rs753084670	in-del	-/T	1.64798e-05	0.00287047	frameshift-variant, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101207	GTGAAGAAGACGAAG[-/T]AAGTGCTGGAGAAAA	2177
rs753099736	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10045135	GGTTGCCCTGAATAC[A/C]CGCCCAATGTTTTCT	2177
rs753106716	in-del	-/A	1.64735e-05	0.00286993	frameshift-variant, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088463	CTTCCCTTGCCAGAC[-/A]AATTCCTCTGTCGGG	2177
rs753209499	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097376	CACCTCTGCAGTCTC[A/G]ACCATAAGAGACAGG	2177
rs753223864	snp	C/G	1.64743e-05	0.00287	missense	FANCD2	GRCh38.p7	3:10046652	TACATTGACAGGGTG[C/G]TAAGAAATAAGATTC	2177
rs753236837	snp	C/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084582	TGGCATTAGAGGCGT[C/G]AGCCACCATACCTGG	2177
rs753252480	snp	A/C			missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098766	AGAGCACAGCAGATG[A/C]GAGTGAGGATGACAT	2177
rs753254982	snp	A/G	1.64727e-05	0.00286986	missense, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10081365	TAGCTGCTGAGAATC[A/G]CGGTGTAGTTGATGG	2177
rs753272541	snp	A/G	1.66916e-05	0.00288886	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098723	ATTCACATTTAGGGT[A/G]AAGAGATTAAGTCCC	2177
rs753320021	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10079841	AACAAAATGAGAAAA[C/T]CTTGGGTCTTGGGTA	2177
rs753336850	snp	C/T	1.64893e-05	0.0028713	missense	FANCD2	GRCh38.p7	3:10064803	GGATTGCCATAAACC[C/T]CCTGCCGCTGCTGTT	2177
rs753343425	snp	C/T	4.98467e-05	0.00499208	missense	FANCD2	GRCh38.p7	3:10065947	TCATTCATGTGTTCT[C/T]TCATATTTCTTACTC	2177
rs753389450	snp	A/C	1.68764e-05	0.00290481	missense	FANCD2	GRCh38.p7	3:10039286	CATTTTAGCAAGAAC[A/C]GTGATGAAATCAACA	2177
rs753405102	snp	A/C	1.69375e-05	0.00291006	intron-variant	FANCD2	GRCh38.p7	3:10043180	CTCACACAGGATGTC[A/C]CAATTTTCTGACATC	2177
rs753407583	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093475	CAATGGATGCATTTT[C/T]CCACCCTAGTTGGAT	2177
rs753410450	in-del	-/T	1.67365e-05	0.00289275	utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101312	GCCAGCCTGTGATCA[-/T]TTTTGTGTTAGAGTT	2177
rs753419823	snp	A/C/G	3.38182e-05	0.00411195	intron-variant	FANCD2	GRCh38.p7	3:10060279	TTTTCATCTTTCTTC[A/C/G]TCATCTCATTGCAGG	2177
rs753430541	snp	A/G	1.65669e-05	0.00287805	intron-variant	FANCD2	GRCh38.p7	3:10064882	AGGCCAAAAGTCAGT[A/G]TAGTTTTTCTTTTCT	2177
rs753435096	snp	C/T	1.69375e-05	0.00291006	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090243	TCTTCCCAGGTAGTT[C/T]TAAGCAGTGCATCAT	2177
rs753440802	in-del	-/ATGGTATCGC			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026748	TTTTCTGGAAGCCAG[-/ATGGTATCGC]ACGTGTTAAAGGCGG	2177
rs753495005	snp	C/T	1.65373e-05	0.00287548	intron-variant	FANCD2	GRCh38.p7	3:10036350	GAAAAGTAAGTGGCG[C/T]TATTATGGAATGTTC	2177
rs753527115	snp	A/G	1.64727e-05	0.00286986	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088844	ATCTACCTGGAGCAC[A/G]CAGAGAGCATTCTGA	2177
rs753558215	snp	A/G	1.65004e-05	0.00287227	intron-variant	FANCD2	GRCh38.p7	3:10063937	TTGTCTTTTCTTAAA[A/G]CAATAAAGCATGAGA	2177
rs753560188	snp	A/G	1.64741e-05	0.00286998	intron-variant, synonymous-codon	FANCD2, FANCD2OS	GRCh38.p7	3:10098833	ATCTCTACAAAACCC[A/G]CCAGAGTCTGGCACT	2177
rs753560349	snp	C/T	1.64806e-05	0.00287054	missense	FANCD2	GRCh38.p7	3:10063819	TTGCAGTTGGTTCAT[C/T]CCTGCAGTGAGCAGT	2177
rs753560435	snp	C/G	1.64741e-05	0.00286998	missense	FANCD2	GRCh38.p7	3:10047982	TCACTCTCTAGACCA[C/G]AGTATAATTTCATTT	2177
rs753568480	snp	A/T			synonymous-codon	FANCD2	GRCh38.p7	3:10073299	ATCCTCCTCTGACAC[A/T]CTTTCAGAAGAGAAA	2177
rs753601224	in-del	-/TG	4.94654e-05	0.00497295	intron-variant	FANCD2	GRCh38.p7	3:10039860	GGTGGATAAACCCTC[-/TG]TCATCATCTAAGTGA	2177
rs753610424	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10029806	TGTTGTTGTTTGAGA[C/T]GGAGTCTCACTCTGT	2177
rs753651489	snp	C/T	3.29549e-05	0.00405911	missense	FANCD2	GRCh38.p7	3:10048040	AAGTTTTTTGACACG[C/T]ACTGCCAGCAGGTAT	2177
rs753657093	snp	C/T	1.65288e-05	0.00287474	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093236	AAAGAGGCTGGAGTG[C/T]TCAAAGGAGCAGATC	2177
rs753657326	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10056998	TAGCTGGGACCATAG[A/G]TGTGCACCACCATGC	2177
rs753671191	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10069043	GAAACTACTAACAAC[A/C]ACAACAAAAAACATT	2177
rs753672518	snp	A/C	1.65187e-05	0.00287386	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085963	TTGTTGTCCCAAGAA[A/C]CTCCTAGGAACAGGA	2177
rs753694185	in-del	-/T	1.66963e-05	0.00288927	intron-variant	FANCD2	GRCh38.p7	3:10043819	TGTGACTCTCTCCTG[-/T]TTTTTTCAGGCAATT	2177
rs753729530	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10058050	CGGCAAAGATCATTT[A/T]TCTTCCAGGGATGTA	2177
rs753731984	snp	A/C	1.70061e-05	0.00291595	intron-variant	FANCD2	GRCh38.p7	3:10073243	CACTTTTCTCTTTTT[A/C]ATATAAAAGAAAGGA	2177
rs753781035	snp	A/G			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026876	ATAAATAAAAAGTTT[A/G]GCACAGGGCCCGGTA	2177
rs753784107	snp	A/C/G	3.351e-05	0.00409317	intron-variant	FANCD2	GRCh38.p7	3:10039919	CAGTATGCAAAGAGC[A/C/G]GTAGTAATATGGTCT	2177
rs753784509	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10041149	CAGTGAGCTGTGATG[A/G]CACCACTGTAACTGT	2177
rs753809948	snp	A/C	3.29468e-05	0.00405861	missense	FANCD2	GRCh38.p7	3:10078147	GATCTCTCCCAGAAG[A/C]TGGAGAGTATGCTGA	2177
rs753830492	in-del	-/A	6.59196e-05	0.00574068	frameshift-variant	FANCD2	GRCh38.p7	3:10063808	TGACCTCCTTGTTGC[-/A]GTTGGTTCATTCCTG	2177
rs753832851	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10040253	ATGTTAGCCAGGATG[A/G]TCTCGATCTCCTGAC	2177
rs753860269	snp	C/T	1.6528e-05	0.00287467	synonymous-codon	FANCD2	GRCh38.p7	3:10032905	TGAAGAAAATGACAG[C/T]ATCTTTGTAAAGCTT	2177
rs753964157	snp	A/C	1.64746e-05	0.00287002	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088513	AGAGAAGAGCAACAT[A/C]TCTAATGACCAGCTC	2177
rs753982841	snp	C/T	3.39104e-05	0.00411753	intron-variant	FANCD2	GRCh38.p7	3:10046548	CTGATTTGTTAACTG[C/T]TTTTCTGTTGTTGCA	2177
rs753984486	snp	G/T	1.64827e-05	0.00287073	intron-variant	FANCD2	GRCh38.p7	3:10039848	GGAAAGAACTCAGGT[G/T]GATAAACCCTCTGTC	2177
rs754006641	in-del	-/TT	1.71502e-05	0.00292827	intron-variant	FANCD2	GRCh38.p7	3:10073238	TGAGTCACTTTTCTC[-/TT]TTTAATATAAAAGAA	2177
rs754065798	snp	C/T	1.67363e-05	0.00289272	intron-variant	FANCD2	GRCh38.p7	3:10052345	ATTTTAAGGGAAAAA[C/T]GTTAGCTGCTAGCCT	2177
rs754092835	snp	C/T	1.64882e-05	0.00287121	intron-variant	FANCD2	GRCh38.p7	3:10064347	TTTTTGTTTGTTTGC[C/T]TCCTGAAGGAATGGG	2177
rs754172769	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088238	GTTGGGGTGGGACGT[A/G]TTGAGCCTTAGGCAA	2177
rs754206628	snp	C/T	8.2392e-05	0.00641788	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10081492	GAAGTGTGGAGAGAA[C/T]TGAGTATATACTTGC	2177
rs754258198	snp	C/T	4.94181e-05	0.00497057	missense	FANCD2	GRCh38.p7	3:10064423	ACTCCTGTGTTGTTC[C/T]GGAAGGGTAGGTATT	2177
rs754335505	snp	A/T	1.64746e-05	0.00287002	intron-variant	FANCD2	GRCh38.p7	3:10042552	TTTCTGTGCTTTTAA[A/T]TTTTAGGTTCGCCAG	2177
rs754337112	snp	A/G	1.92766e-05	0.0031045	missense	FANCD2	GRCh38.p7	3:10067314	CTGGAAAAGTACTTG[A/G]CAGGTAAGAGAAGTG	2177
rs754341039	snp	C/T	1.64776e-05	0.00287028	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088413	AATGAGGTCAAGTTC[C/T]CATATGTAAGATTCC	2177
rs754358457	snp	C/T	1.64735e-05	0.00286993	synonymous-codon	FANCD2	GRCh38.p7	3:10042630	GATAATAAAGTTCAT[C/T]CTTCATTCCGTAACA	2177
rs754401436	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10066742	TGTTTTTTGTTTTTT[C/T]GAGACAGAGTCTTGC	2177
rs754406685	snp	A/C			upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10024760	ATACAGGATAATTTA[A/C]GATTGCTTATTTAGG	2177
rs754413904	snp	C/G	1.64803e-05	0.00287052	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10081503	AGAACTGAGTATATA[C/G]TTGCTTTTATTTGAC	2177
rs754421685	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10077238	ACCCTGTCTCAAATA[C/T]AAGTAAATAAATAAA	2177
rs754425975	snp	A/G	1.65111e-05	0.0028732	missense	FANCD2	GRCh38.p7	3:10072883	CAGTCACCCCAGACT[A/G]TGTCCCTCCTCTTGG	2177
rs754430808	snp	C/T	3.82409e-05	0.00437253	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095321	TGCCTGTTGGCTTAA[C/T]CTGCAGTTGCTATTG	2177
rs754471271	in-del	-/AG			intron-variant	FANCD2	GRCh38.p7	3:10067780	TCCAGCCTGGGTGAC[-/AG]AGCGAGACTCCCATC	2177
rs754474363	in-del	-/CTGAGGGCTCCTTCA			intron-variant	FANCD2	GRCh38.p7	3:10064073	TCTCACGGCTCTTCT[-/CTGAGGGCTCCTTCA]CTTAATAACAATCAC	2177
rs754488028	snp	C/G	1.64735e-05	0.00286993	missense	FANCD2	GRCh38.p7	3:10042658	ACAGCCATGGATACA[C/G]TTGAGGTATGCTCTT	2177
rs754523292	snp	A/G	3.45113e-05	0.00415385	missense	FANCD2	GRCh38.p7	3:10065975	CTCTCAACTGGTTCC[A/G]AGAGGTGAGCAGAGT	2177
rs754550122	snp	A/G	6.58903e-05	0.00573941	missense	FANCD2	GRCh38.p7	3:10064428	TGTGTTGTTCCGGAA[A/G]GGTAGGTATTGTTTA	2177
rs754574116	snp	C/T	1.64727e-05	0.00286986	missense, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10081395	GACCAGGAGTGAAAG[C/T]TCAGGAGTACCACAT	2177
rs754575756	snp	A/T	3.34778e-05	0.00409119	intron-variant	FANCD2	GRCh38.p7	3:10043028	TGAGCAGAAAACCAT[A/T]GCTAATATTTACTTT	2177
rs754588492	snp	A/G			intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10099532	TGGGAGGCCGATGTG[A/G]GCAGATCACAAGGTC	2177
rs754592042	snp	C/T	8.29786e-05	0.00644068	intron-variant	FANCD2	GRCh38.p7	3:10028611	GTAACTTCTGTTTCC[C/T]GATTTTGCTCTAGGA	2177
rs754592456	snp	A/G	1.64735e-05	0.00286993	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092162	GACTCAGAGGTGCCC[A/G]TATATTTGGCTGCCC	2177
rs754606069	snp	A/G	3.29473e-05	0.00405864	intron-variant, stop-gained	FANCD2, FANCD2OS	GRCh38.p7	3:10098884	TGTTCTAAGTTGGTG[A/G]AGCAGAACTTTGCCT	2177
rs754613426	snp	A/G	0.000116241	0.00762281	intron-variant	FANCD2	GRCh38.p7	3:10028772	AGCAATGTGTGAGGC[A/G]TGTGAGAGATATAAA	2177
rs754665005	snp	A/G	6.09069e-05	0.00551813	intron-variant	FANCD2	GRCh38.p7	3:10067326	TTGGCAGGTAAGAGA[A/G]GTGTCCTATACTGGT	2177
rs754681444	snp	G/T	1.64779e-05	0.00287031	intron-variant	FANCD2	GRCh38.p7	3:10039693	TCTGGGTAATGTGCT[G/T]CAGTTCTAATAGTGT	2177
rs754682231	snp	C/T	1.64727e-05	0.00286986	intron-variant	FANCD2	GRCh38.p7	3:10047903	TTTTCTCTCTCTACT[C/T]TTCCCCACTCAAGGT	2177
rs754726372	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10048190	TCAATTCTAGTCCCA[A/G]CCTTGATGAAAGGAA	2177
rs754740540	snp	C/T	1.64727e-05	0.00286986	missense	FANCD2	GRCh38.p7	3:10065420	CGCTGTGCCTGGCTC[C/T]GTATTTCCGGTTACT	2177
rs754800158	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10057046	ATTTTGGTAGACATT[A/T]TGTTTTGTCATGTTA	2177
rs754809720	snp	A/C	1.64811e-05	0.00287059	missense	FANCD2	GRCh38.p7	3:10028682	AAAAGAAGACTGTCA[A/C]AATCTGAGGATAAAG	2177
rs754860692	snp	A/T	0.00012846	0.00801335	intron-variant	FANCD2	GRCh38.p7	3:10062129	TATAATAATAATTTA[A/T]AAAAAAATTCTTTGT	2177
rs754863896	snp	A/T	8.23635e-05	0.00641677	intron-variant, missense	FANCD2, FANCD2OS	GRCh38.p7	3:10098871	GCATTTTGTTAATTG[A/T]TCTAAGTTGGTGGAG	2177
rs754878606	snp	A/G	1.75253e-05	0.00296012	intron-variant	FANCD2	GRCh38.p7	3:10046735	CTTAGTAAGTGTCAG[A/G]GACTATTGATTTTTA	2177
rs754898225	snp	A/T	1.64798e-05	0.00287047	intron-variant	FANCD2	GRCh38.p7	3:10065361	GTAATACACCTATGA[A/T]GTGTGGTCTAGAAAT	2177
rs754908032	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10048342	TGGTTTTGCTCTTCA[C/T]GCCCAGGCTGGAGTG	2177
rs754937371	snp	A/T	3.33645e-05	0.00408425	missense	FANCD2	GRCh38.p7	3:10039319	CCTCGACTCATTGTC[A/T]GTCAACTAAAATGGC	2177
rs755009168	snp	C/T	3.29489e-05	0.00405874	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087104	CATAGGATACTATTG[C/T]ATTTGTTTGTTTTTC	2177
rs755018272	in-del	-/TTGT			intron-variant	FANCD2	GRCh38.p7	3:10031614	GTACCTGTTTGTTTC[-/TTGT]TTCTTATTTCTTTTT	2177
rs755027159	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10031970	TCCTCCTCAGCCTCC[C/T]GAGTAGTTGGTATTA	2177
rs755028947	snp	A/G	1.6492e-05	0.00287154	synonymous-codon	FANCD2	GRCh38.p7	3:10034515	CTTTCAGACCCTGAG[A/G]AGACACCCTTCCTAT	2177
rs755031951	in-del	-/TT			splice-donor-variant	FANCD2	GRCh38.p7	3:10046723	TCTGTTCATTACTTA[-/TT]GTAAGTGTCAGAGAC	2177
rs755038050	snp	A/G	6.08772e-05	0.00551678	intron-variant	FANCD2	GRCh38.p7	3:10074485	TAAAATTCGATTAAT[A/G]TAGAAGATTTATATA	2177
rs755046306	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10039421	ATCTTTTGGAGGTTG[C/T]ATTTTTTTTTCTTTC	2177
rs755066005	snp	C/G			upstream-variant-2KB, nc-transcript-variant	FANCD2, CIDECP	GRCh38.p7	3:10026131	ACGAAGAGTGATAAC[C/G]ATGGGTAGGACCACC	2177
rs755084399	in-del	-/A			intron-variant	FANCD2	GRCh38.p7	3:10057790	ATTACTATTAAAATT[-/A]AAAAAAAACAGCATA	2177
rs755105473	snp	C/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082650	GCCAGGACCCCCACT[C/G]TTCTTGATCCCCAGC	2177
rs755140002	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10072044	GGATTACAGGCATGA[G/T]CCAGAGAGCCCAGCC	2177
rs755150961	snp	A/G	1.65389e-05	0.00287562	intron-variant	FANCD2	GRCh38.p7	3:10034420	GGGTTTTTAGAGAAG[A/G]AAAACTATGGTAGGA	2177
rs755205321	snp	C/T	9.88468e-05	0.00702948	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087214	TCATCAGACTTTTGA[C/T]GGTTATTTTGGAGAA	2177
rs755266690	snp	C/T			upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10024920	CTGAACAAGTGTTTT[C/T]TCGTTTGTTTTTCTG	2177
rs755267697	snp	C/G	1.64817e-05	0.00287064	missense	FANCD2	GRCh38.p7	3:10063900	CATGAAAAGCTGGAT[C/G]CAAAAGCCCTGGTAA	2177
rs755269517	snp	G/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090228	CTTTTGGTTCCTGGT[G/T]CTTCCCAGGTAGTTC	2177
rs755280943	in-del	-/CAGA	1.6591e-05	0.00288015	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087316	ATGAATAGGACTAAT[-/CAGA]ATCTCACACTTACAA	2177
rs755294483	in-del	-/TA			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10028050	AAACCCTGTCTCTAC[-/TA]AAAAAAAAAAAAAAA	2177
rs755295382	snp	A/C	4.94238e-05	0.00497086	missense	FANCD2	GRCh38.p7	3:10046645	AAAGAAGTACATTGA[A/C]AGGGTGCTAAGAAAT	2177
rs755297230	snp	A/T	3.30087e-05	0.00406242	intron-variant	FANCD2	GRCh38.p7	3:10041591	TCTGTTCAAACCATT[A/T]TACAACTTTTTTCTT	2177
rs755335827	snp	C/T	3.31323e-05	0.00407002	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081058	TAGTTTCTGAGACGC[C/T]ATCCAGCAGTTTCTT	2177
rs755350165	snp	C/T	1.72036e-05	0.00293283	stop-gained	FANCD2	GRCh38.p7	3:10065974	ACTCTCAACTGGTTC[C/T]GAGAGGTGAGCAGAG	2177
rs755369640	snp	G/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096120	AGAGGAACTAGAGGT[G/T]TTGGTGGTATGTCTT	2177
rs755385600	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10055614	TCAGGAGATCGAGAC[C/T]ATCCTGGCTAACACG	2177
rs755387164	snp	A/C	6.59055e-05	0.00574007	missense	FANCD2	GRCh38.p7	3:10041693	AGCCTCCGACTTGAC[A/C]CAAACTTCCTATTGA	2177
rs755389495	snp	C/T	1.64727e-05	0.00286986	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088834	TCAATGCAGTATCTA[C/T]CTGGAGCACACAGAG	2177
rs755459217	snp	G/T	1.648e-05	0.0028705	missense, downstream-variant-500B	FANCD2, FANCD2OS	GRCh38.p7	3:10081167	AAGAAATTGTTCATT[G/T]TGTTTTTCAACTGCT	2177
rs755464133	snp	C/T	1.6483e-05	0.00287076	stop-gained	FANCD2	GRCh38.p7	3:10063840	AGTGAGCAGTCTCCT[C/T]AGGCCTCTGCACTTT	2177
rs755486346	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082909	TTGAACAATTTATCA[A/G]AGAGACTTATAGATG	2177
rs755516280	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10063273	AATCCCATCTCTAAT[A/G]AAAGTACAAAAAAAT	2177
rs755520788	snp	A/G	1.73893e-05	0.00294862	intron-variant	FANCD2	GRCh38.p7	3:10060263	CTGTGCCATTCCAGC[A/G]TTTTCATCTTTCTTC	2177
rs755531020	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094988	ATGCAGGTCTTATAA[C/T]TCTCAGATTGATACA	2177
rs755533360	snp	A/G	1.66443e-05	0.00288477	splice-donor-variant	FANCD2	GRCh38.p7	3:10043151	TAAAGGACGAGCAAG[A/G]TAAAGAGCTCATCCT	2177
rs755550249	in-del	-/G	1.65153e-05	0.00287356	intron-variant	FANCD2	GRCh38.p7	3:10074715	TTTAATCTTCTTTCA[-/G]AAAGTTCCTCAGGTC	2177
rs755572622	snp	C/T	1.64735e-05	0.00286993	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096425	CTCACTCTCAACAAT[C/T]GTAGAGAGGCTTTCT	2177
rs755673512	in-del	-/TGCTC	1.64789e-05	0.0028704	frameshift-variant, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088530	TAATGACCAGCTCCA[-/TGCTC]TGCTCTGCTCTGGTG	2177
rs755678967	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10077490	AACCTGGGACGCAGA[A/G]GTTGTAGTGAGCCAA	2177
rs755710428	snp	C/T			upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025175	TGCCCAGGCTGGTCT[C/T]GAACTCCAGGGCTCA	2177
rs755711920	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10063480	AGAGAAAACAGAGAG[C/T]CTTGCATGTAAAGCA	2177
rs755725087	snp	C/T	0.000181997	0.00953758	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088553	CTCTGGTGAGATGTT[C/T]GGTTTCTTCCAATGA	2177
rs755748094	snp	A/G	9.88468e-05	0.00702948	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085877	ATGTCCTTAGTAGCC[A/G]ACTGAAACAGGGAGA	2177
rs755764644	snp	C/T	1.64993e-05	0.00287218	synonymous-codon	FANCD2	GRCh38.p7	3:10072918	TTTGATGTGGAAACT[C/T]TAGATATAACACCTC	2177
rs755767180	snp	C/T	0.000172393	0.00928261	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098707	ACCATTTTCTTGGTC[C/T]ATTCACATTTAGGGT	2177
rs755797932	snp	A/G	3.30273e-05	0.00406356	missense	FANCD2	GRCh38.p7	3:10043066	TAATTTCTGAGCTTC[A/G]GGAGAAGTTGGATCT	2177
rs755811046	snp	A/G	0.00012818	0.00800461	intron-variant	FANCD2	GRCh38.p7	3:10032342	CTGGAGTGCAGTGGT[A/G]ATATCATAGCTCACT	2177
rs755816529	snp	C/G	1.64741e-05	0.00286998	intron-variant	FANCD2	GRCh38.p7	3:10064451	ATTGTTTACCTGCTG[C/G]CTTGGTTGCACTGGT	2177
rs755821273	snp	A/G	4.94197e-05	0.00497066	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092166	CAGAGGTGCCCATAT[A/G]TTTGGCTGCCCCAGA	2177
rs755856987	snp	A/G	1.75366e-05	0.00296108	intron-variant	FANCD2	GRCh38.p7	3:10073226	TTATTAATTACTTGA[A/G]TCACTTTTCTCTTTT	2177
rs755911397	snp	A/G	1.64814e-05	0.00287061	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101203	GATGGTGAAGAAGAC[A/G]AAGTAAGTGCTGGAG	2177
rs755926702	in-del	-/CAGGTGGATAAACC	1.64806e-05	0.00287054	intron-variant	FANCD2	GRCh38.p7	3:10039843	TGTGGGGAAAGAACT[-/CAGGTGGATAAACC]CTCTGTCATCATCTA	2177
rs755975980	snp	A/G	6.58913e-05	0.00573945	missense	FANCD2	GRCh38.p7	3:10065429	TGGCTCCGTATTTCC[A/G]GTTACTGAGACTTTG	2177
rs755992976	snp	C/T	1.64741e-05	0.00286998	stop-gained	FANCD2	GRCh38.p7	3:10047980	CTTCACTCTCTAGAC[C/T]AGAGTATAATTTCAT	2177
rs756030123	snp	G/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088694	GGAACATGTGGATCT[G/T]AAGATCCTCTGGTTC	2177
rs756066137	snp	C/T	1.84391e-05	0.00303632	intron-variant	FANCD2	GRCh38.p7	3:10062144	AAAAAAAATTCTTTG[C/T]TTTTAGAAGTGAATC	2177
rs756071447	in-del	-/A			intron-variant	FANCD2	GRCh38.p7	3:10047513	TCTTGATCTTCTTTT[-/A]AAAAAAATCAGCTTA	2177
rs756078235	snp	A/G	4.9445e-05	0.00497193	missense	FANCD2	GRCh38.p7	3:10028695	CAAAATCTGAGGATA[A/G]AGAGAGCCTGACAGA	2177
rs756129956	snp	A/G	1.64735e-05	0.00286993	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085774	TCCAAGTAGTTTTCC[A/G]GAAACTAAGCTAACC	2177
rs756165037	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10044541	CCTGGCCTGGTGGCA[C/G]ACGCCACTGCACTCC	2177
rs756178348	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10051656	CTGGTTGTGAGGGAG[A/G]TATTTTTTAGATGAG	2177
rs756183300	snp	A/T	1.64781e-05	0.00287033	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088405	AAAGCAAGAATGAGG[A/T]CAAGTTCCCATATGT	2177
rs756201843	snp	C/T	1.65184e-05	0.00287384	intron-variant	FANCD2	GRCh38.p7	3:10074713	AATTTAATCTTCTTT[C/T]AGAAAGTTCCTCAGG	2177
rs756202265	snp	C/T	3.295e-05	0.00405881	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087220	GACTTTTGATGGTTA[C/T]TTTGGAGAAATCAAC	2177
rs756218874	snp	A/T			synonymous-codon	FANCD2	GRCh38.p7	3:10042591	GGATAAGTTGTCGTC[A/T]ATTAGATTGGAGGAT	2177
rs756231051	snp	C/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082538	TGACTCCTGCTATTC[C/G]ACTTATTATGTTATA	2177
rs756233563	snp	A/C			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094866	GAACAAAATACTCAC[A/C]ATATTTGGTTGGTCC	2177
rs756293137	in-del	-/TTTT	0.000223647	0.0105723	intron-variant	FANCD2	GRCh38.p7	3:10062248	TTTCTTTTTCCTGTC[-/TTTT]TTTTTTTTTTAGAGA	2177
rs756307770	snp	C/T	6.7059e-05	0.00579008	missense	FANCD2	GRCh38.p7	3:10043847	ATTGAAAACACTGCC[C/T]CAGTATCTGAACACA	2177
rs756313149	snp	A/C	3.51074e-05	0.00418957	missense	FANCD2	GRCh38.p7	3:10034786	GTGAGCGTCTGCAGG[A/C]TGAGGAAGCCAGGTG	2177
rs756334086	snp	G/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093243	CTGGAGTGCTCAAAG[G/T]AGCAGATCTCAGCCT	2177
rs756336462	snp	C/G			missense	FANCD2	GRCh38.p7	3:10039745	ACCAAGATCATGCAG[C/G]TGATCAGTATTGCTC	2177
rs756347005	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10067976	TAAAATTCAACATCC[C/T]TTCATCATAAAAAAC	2177
rs756355001	snp	A/G	1.6507e-05	0.00287284	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10098984	AATTTTTGGGACCCA[A/G]AAGAAACAACGACAC	2177
rs756374537	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10028885	ACTGAGTTTTTGCCT[C/T]GAATTCTGCGTATAA	2177
rs756389891	snp	G/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081557	GAAAAGAAAGAAAAG[G/T]TTCAAAAATCTTATG	2177
rs756417861	snp	A/T	1.66225e-05	0.00288287	missense	FANCD2	GRCh38.p7	3:10049480	TAAACCCATCTGCTA[A/T]GATGATGAATGCTGT	2177
rs756475711	snp	C/G	1.64825e-05	0.00287071	splice-donor-variant	FANCD2	GRCh38.p7	3:10063912	GATCCAAAAGCCCTG[C/G]TAAAGCCAATTGTCT	2177
rs756475849	snp	C/T			downstream-variant-500B, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10102263	ATTCTCCTGTCTCAG[C/T]CCCCTGTATAGGTGG	2177
rs756498629	snp	C/G	1.65203e-05	0.002874	intron-variant	FANCD2	GRCh38.p7	3:10064331	ACACTCTGCACTGCC[C/G]TTTTTGTTTGTTTGC	2177
rs756513527	snp	A/C	1.65023e-05	0.00287244	missense	FANCD2	GRCh38.p7	3:10034536	CCCTTCCTATCCCAA[A/C]GTATGTATTTTTCCC	2177
rs756530022	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10036014	ATTCGTGTGGATATC[C/T]TTGTAATAAGATATC	2177
rs756558044	snp	A/G	6.62471e-05	0.00575492	missense	FANCD2	GRCh38.p7	3:10060300	TCATTGCAGGATGAC[A/G]TGCACTTGGTGATAA	2177
rs756603905	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10074156	TCACCATCTTGGCCA[G/T]GCAGGTCTCAAACTC	2177
rs756604077	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087003	GTTGCTACTAAAGCA[C/T]CTGAAAATAAGGAGG	2177
rs756614079	snp	A/C	1.64727e-05	0.00286986	missense	FANCD2	GRCh38.p7	3:10049387	AGGAAGTGGTTGGTG[A/C]CTTAGTGACCCATAT	2177
rs756619423	in-del	-/T	1.64781e-05	0.00287033	frameshift-variant, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101247	TAGTGATGAGAGTTA[-/T]GATGACTCTGATTAG	2177
rs756621826	snp	C/T	1.64789e-05	0.0028704	synonymous-codon	FANCD2	GRCh38.p7	3:10041705	GACCCAAACTTCCTA[C/T]TGAAGGTAGAAAAGA	2177
rs756645719	snp	A/G	1.67826e-05	0.00289673	missense	FANCD2	GRCh38.p7	3:10046719	CATTCTCTGTTCATT[A/G]CTTAGTAAGTGTCAG	2177
rs756659525	in-del	-/TTG			intron-variant	FANCD2	GRCh38.p7	3:10051600	CAATGTCGAGAAGCA[-/TTG]TCAAGGAGGAGAGAA	2177
rs756659872	snp	A/G	1.67775e-05	0.00289629	missense	FANCD2	GRCh38.p7	3:10039295	AAGAACAGTGATGAA[A/G]TCAACATACCTCGAC	2177
rs756670695	snp	C/T	1.9991e-05	0.0031615	intron-variant	FANCD2	GRCh38.p7	3:10067201	AGAATGTAATTTGTA[C/T]TTTGCAGATTGTAAA	2177
rs756674236	snp	A/C/G	3.2948e-05	0.00405871	intron-variant, missense	FANCD2, FANCD2OS	GRCh38.p7	3:10098834	TCTCTACAAAACCCA[A/C/G]CAGAGTCTGGCACTG	2177
rs756689535	in-del	-/TTTTTTTTTTC			intron-variant	FANCD2	GRCh38.p7	3:10045102	GTTTTTTTTTTTTTC[-/TTTTTTTTTTC]CTGGAAGCATAGACT	2177
rs756690093	snp	A/G	3.2975e-05	0.00406035	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094404	GATATGCACTGAAGA[A/G]TTGCTCAGAAGATAT	2177
rs756713676	snp	C/T	1.64727e-05	0.00286986	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088845	TCTACCTGGAGCACA[C/T]AGAGAGCATTCTGAA	2177
rs756800614	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10058485	TCTTAAATTTAGGTC[C/T]TTGATCCACTTTGTG	2177
rs756838566	snp	A/G	3.32508e-05	0.00407729	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098728	CATTTAGGGTGAAGA[A/G]ATTAAGTCCCAAAAT	2177
rs756848064	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10077415	CAAAAATTAGTCAGG[C/T]ATGGTGGTGGGCACC	2177
rs756886854	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083814	AATGGCCTTAACCCG[A/G]GAGGTGGAGCTTGCA	2177
rs756892863	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10076358	ATATTTAGGAAACGC[A/T]TCTTGGATCCACAAC	2177
rs756898495	snp	A/C/G	3.29464e-05	0.00405861	splice-acceptor-variant	FANCD2	GRCh38.p7	3:10064728	TGGTTTTTCTCCGCA[A/C/G]TGACTTTCCATTTCC	2177
rs756900653	snp	A/G	4.95086e-05	0.00497512	intron-variant	FANCD2	GRCh38.p7	3:10073384	GAATGATGGGTATCC[A/G]TGAAGGTTTGTGACA	2177
rs756911727	snp	G/T	1.65468e-05	0.00287631	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081087	TTCACTCATAACTCT[G/T]CATTTATTATAGAAC	2177
rs756932742	snp	A/T	1.65559e-05	0.00287709	intron-variant	FANCD2	GRCh38.p7	3:10036356	TAAGTGGCGTTATTA[A/T]GGAATGTTCAAAGTA	2177
rs756935992	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10089883	TTTTCAGTTTATAAA[A/G]CACTTTCACTTTATC	2177
rs756955176	snp	A/G	3.29853e-05	0.00406098	intron-variant	FANCD2	GRCh38.p7	3:10052501	AGCCACATCCAGGTA[A/G]GAGGCAATATGTTGG	2177
rs756966238	snp	A/T	1.65021e-05	0.00287241	synonymous-codon	FANCD2	GRCh38.p7	3:10043100	GCATTGTGTTTTGCC[A/T]TCACGGTTACAGGCT	2177
rs756992197	snp	C/T	1.6476e-05	0.00287014	synonymous-codon	FANCD2	GRCh38.p7	3:10064805	ATTGCCATAAACCTC[C/T]TGCCGCTGCTGTTTT	2177
rs757001820	snp	C/G	1.64795e-05	0.00287045	missense	FANCD2	GRCh38.p7	3:10048048	TGACACGTACTGCCA[C/G]CAGGTATGTTGAAAC	2177
rs757018488	in-del	-/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094611	TTCCTTTTAGCTTGA[-/T]TTTATTGTGCTACTG	2177
rs757027350	in-del	-/A	1.64741e-05	0.00286998	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088805	GTTAATTAGTGGGTC[-/A]AAATATTTGACTCTC	2177
rs757033789	in-del	-/A			intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10099278	AAAATAGAAGTTCTT[-/A]ACGCTTTTTTGTGGT	2177
rs757052617	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10040335	GCCACCGTGCCTGGC[C/G]CCATGTACTTTCTTT	2177
rs757053371	snp	A/T	3.30579e-05	0.00406544	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093237	AAGAGGCTGGAGTGC[A/T]CAAAGGAGCAGATCT	2177
rs757077597	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10067881	TTGTTCAACATATGT[A/G]AATCAATGTGATACC	2177
rs757097513	snp	G/T	1.69691e-05	0.00291278	intron-variant	FANCD2	GRCh38.p7	3:10043185	ACAGGATGTCACAAT[G/T]TTCTGACATCCCACT	2177
rs757102395	snp	A/G	3.37923e-05	0.00411036	intron-variant	FANCD2	GRCh38.p7	3:10073246	TTTTCTCTTTTTAAT[A/G]TAAAAGAAAGGAAAC	2177
rs757103967	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10030394	GAGCCACCATGCCTG[G/T]CCTCATTATGTCATT	2177
rs757127466	snp	C/T	1.64735e-05	0.00286993	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085788	CAGAAACTAAGCTAA[C/T]CCCTCTTACCTTGAC	2177
rs757128928	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10066852	TCTTCAGCCTCCCTA[A/G]TAGCTGGGATTACAG	2177
rs757152429	snp	A/C	1.64803e-05	0.00287052	synonymous-codon	FANCD2	GRCh38.p7	3:10063821	GCAGTTGGTTCATTC[A/C]TGCAGTGAGCAGTCT	2177
rs757168237	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10043966	TCCCCCCTCCAGTCA[C/G]TCTTCTCTCTCTTCC	2177
rs757201786	snp	A/G			intron-variant, downstream-variant-500B	FANCD2, FANCD2OS	GRCh38.p7	3:10100005	TTTCAAGACCAACCC[A/G]AGACCCCATCTCTAC	2177
rs757215059	snp	C/G			utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101468	TTGGCTCACTGCAAC[C/G]TCCATCTCCTAGGTT	2177
rs757237002	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10053721	TTTCTTACCACAAAC[A/T]TTAAGTGCCTATTCT	2177
rs757254800	in-del	-/A	4.99671e-05	0.00499811	intron-variant	FANCD2	GRCh38.p7	3:10039905	GGGTTCTATCACTGC[-/A]GTATGCAAAGAGCAG	2177
rs757271511	snp	A/G	4.94344e-05	0.00497139	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101230	GGAGAAAAGGAGCAA[A/G]ATAGTGATGAGAGTT	2177
rs757311892	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10060023	AAATACAAAATAAGC[C/T]GGGCATGGTGGCGGG	2177
rs757337813	snp	A/T	3.46783e-05	0.00416388	intron-variant	FANCD2	GRCh38.p7	3:10065846	TAAAGGTAGTTGGAA[A/T]TGTTTGTTCTCTCTC	2177
rs757359450	snp	A/C	1.64852e-05	0.00287094	intron-variant	FANCD2	GRCh38.p7	3:10039855	ACTCAGGTGGATAAA[A/C]CCTCTGTCATCATCT	2177
rs757421526	snp	C/T	0.000214304	0.0103492	intron-variant	FANCD2	GRCh38.p7	3:10063758	GGAAAGATTGGCAGC[C/T]CAAGGTTTAAACCAT	2177
rs757423861	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10074778	GAGGAGAGAAGTTAG[A/G]CTGACTTTTAAAGCC	2177
rs757435802	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10080549	TCCAAGATGGGTGGA[C/T]TGCTTGAGCTCAGGA	2177
rs757440705	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10042363	TTTATTGCCCGTCTA[C/T]TTTTGATGAAGCTGT	2177
rs757451046	snp	A/G	1.67312e-05	0.00289229	intron-variant	FANCD2	GRCh38.p7	3:10032797	AATTTTTCCTTTACT[A/G]TTTGCCATATTCTTG	2177
rs757471770	snp	A/T	1.64754e-05	0.00287009	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088519	GAGCAACATCTCTAA[A/T]GACCAGCTCCATGCT	2177
rs757499508	snp	A/G	1.64754e-05	0.00287009	stop-gained, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092206	AGAAACTCCTCTACT[A/G]GAACATGGCTGTTCG	2177
rs757567225	in-del	-/CT	1.64822e-05	0.00287068	frameshift-variant	FANCD2	GRCh38.p7	3:10063844	GCAGTCTCCTCAGGC[-/CT]CTCTGCACTTTACTA	2177
rs757581413	snp	C/G	1.94049e-05	0.00311481	intron-variant	FANCD2	GRCh38.p7	3:10034824	GAGGCATGGAATCTT[C/G]CTGAAATTCAGTCTG	2177
rs757582716	snp	A/G	6.58924e-05	0.0057395	missense	FANCD2	GRCh38.p7	3:10078151	TCTCCCAGAAGCTGG[A/G]GAGTATGCTGACACC	2177
rs757585053	in-del	-/TGC	1.74339e-05	0.0029524	intron-variant	FANCD2	GRCh38.p7	3:10060450	AAGATCAGTTAATCT[-/TGC]TAACTAAGTGTTACA	2177
rs757608146	snp	A/G	1.66214e-05	0.00288278	missense	FANCD2	GRCh38.p7	3:10049491	GCTATGATGATGAAT[A/G]CTGTCTTTGTAAAGG	2177
rs757623854	snp	A/C	1.66112e-05	0.00288189	intron-variant	FANCD2	GRCh38.p7	3:10052358	AATGTTAGCTGCTAG[A/C]CTCATTGTTGGCATC	2177
rs757629456	in-del	-/C			intron-variant	FANCD2	GRCh38.p7	3:10075853	ATCCTGCCTCAGCCT[-/C]CCAAGTAGCTGGGAC	2177
rs757694100	snp	A/C/G/T	5.03297e-05	0.00501627	intron-variant	FANCD2	GRCh38.p7	3:10043630	TATCAAGGAGGAAAT[A/C/G/T]AGTGGCAATTAGTGA	2177
rs757694369	snp	C/G	1.96659e-05	0.00313569	splice-donor-variant	FANCD2	GRCh38.p7	3:10067318	AAAAGTACTTGGCAG[C/G]TAAGAGAAGTGTCCT	2177
rs757697678	snp	A/G	1.65173e-05	0.00287374	intron-variant	FANCD2	GRCh38.p7	3:10034555	TGTATTTTTCCCCTG[A/G]TATTTTTGCTTGTGC	2177
rs757739892	snp	A/G	1.74464e-05	0.00295345	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095154	TCTTGAATCTAAAAT[A/G]AAATCAGGACATTTC	2177
rs757740309	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10035909	TTAATTATCTGATTA[C/T]TTTAACGTTGCCTTG	2177
rs757745982	snp	C/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084388	CCTCTGACTCCCAGG[C/G]TATAAATCCTCCCAC	2177
rs757748145	snp	A/G			synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098752	CCAAAATTCCCAGGA[A/G]AGCACAGCAGATGAG	2177
rs757782326	snp	C/T	4.94588e-05	0.00497262	intron-variant	FANCD2	GRCh38.p7	3:10064349	TTTGTTTGTTTGCTT[C/T]CTGAAGGAATGGGTT	2177
rs757795334	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10037329	ACAGTAAAATAAATG[C/T]ATTTTTTCCTACTCT	2177
rs757808149	snp	A/G	1.68519e-05	0.0029027	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090356	ACGGTGAAAAAAATT[A/G]AGCCTGGCACAGCAG	2177
rs757846525	in-del	-/A			intron-variant	FANCD2	GRCh38.p7	3:10059425	AGAAATAATAACAAT[-/A]AAAGATATTATTATT	2177
rs757848745	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10067784	GCCTGGGTGACAGAG[C/T]GAGACTCCCATCTCA	2177
rs757853819	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10036217	CCTCAGCCTCCCAAG[A/T]AGCTGGGATTATACA	2177
rs757869342	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10048873	ACTATTATGGAGTGA[C/T]AGTATAAAGGGAGAA	2177
rs757885302	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10035719	CTCTTCTCCCCTACT[C/G]TTAATCTTTTCACAC	2177
rs757887960	snp	A/G	3.2981e-05	0.00406071	missense, downstream-variant-500B	FANCD2, FANCD2OS	GRCh38.p7	3:10081211	AACCACCTGGAGAAC[A/G]TTCACAACTATTTTC	2177
rs757888823	snp	A/G	3.51265e-05	0.00419071	missense	FANCD2	GRCh38.p7	3:10067216	CTTTGCAGATTGTAA[A/G]TGCCTTCTGCCAGGA	2177
rs757891672	snp	G/T	1.64738e-05	0.00286995	missense	FANCD2	GRCh38.p7	3:10042559	GCTTTTAATTTTTAG[G/T]TTCGCCAGTTGGTGA	2177
rs757895262	in-del	-/A			intron-variant	FANCD2	GRCh38.p7	3:10069133	ACAGGCAACCAAAGC[-/A]AAAATGGACAAATGG	2177
rs757922735	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10040957	CCAGCATGTTGGGCG[A/G]CTGAAGTGGGTGGGT	2177
rs757950223	snp	A/G			intron-variant, downstream-variant-500B	FANCD2, FANCD2OS	GRCh38.p7	3:10099807	TGTCACAATTCAGGT[A/G]GGTTATAGACACCAA	2177
rs758000306	snp	C/T	1.64727e-05	0.00286986	missense, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10081374	AGAATCACGGTGTAG[C/T]TGATGGACCAGGAGT	2177
rs758004763	snp	A/C			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088251	GTGTTGAGCCTTAGG[A/C]AAATGAGTTTATGTC	2177
rs758011243	in-del	-/GCTC			intron-variant	FANCD2	GRCh38.p7	3:10069459	ACCCTAGTTAAGATG[-/GCTC]CCTCTCCCCCTCCCC	2177
rs758015233	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10037422	AATTAGTTCAGGCAT[C/T]GATTCGGAAGAGCAA	2177
rs758034351	snp	A/T	4.94637e-05	0.00497287	intron-variant	FANCD2	GRCh38.p7	3:10047888	GTTTCCTACAGCTTC[A/T]TTTCTCTCTCTACTC	2177
rs758121289	in-del	-/C			frameshift-variant	FANCD2	GRCh38.p7	3:10052414	ATCTGGATAACATAT[-/C]CCCCTCAGCAAATAC	2177
rs758130998	snp	C/G			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027902	AGAGTGAGACTCCGT[C/G]TCAAAAAAAAAAAAA	2177
rs758136121	snp	A/G	3.32209e-05	0.00407546	intron-variant	FANCD2	GRCh38.p7	3:10036369	TATGGAATGTTCAAA[A/G]TACCCTGATGTACTT	2177
rs758140679	snp	A/G	0.000150006	0.00865914	intron-variant	FANCD2	GRCh38.p7	3:10060406	TGGCGGCAGACAGGT[A/G]CACGTGGAGATTCTG	2177
rs758142258	snp	A/G	1.66194e-05	0.00288261	intron-variant	FANCD2	GRCh38.p7	3:10043480	TCCTCTCTGCTACTT[A/G]TAGTTCCTCAGGAAA	2177
rs758161925	in-del	-/TAC			intron-variant	FANCD2	GRCh38.p7	3:10074919	TTACATTTAGGTTAC[-/TAC]TACTACTACTACTAC	2177
rs758190656	snp	G/T	3.29821e-05	0.00406078	missense	FANCD2	GRCh38.p7	3:10074562	AGAAAAGACATCATT[G/T]TTACTACATAATTCC	2177
rs758194192	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10041313	GATTTCATTGTAAAT[C/G]TTTTGGGTTTTCTTT	2177
rs758210208	snp	C/T	3.30431e-05	0.00406454	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098743	GATTAAGTCCCAAAA[C/T]TCCCAGGAGAGCACA	2177
rs758228060	snp	C/G	1.67287e-05	0.00289207	missense	FANCD2	GRCh38.p7	3:10039304	GATGAAATCAACATA[C/G]CTCGACTCATTGTCA	2177
rs758248381	snp	A/G	6.58989e-05	0.00573978	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087092	ATATCTGTGACACAT[A/G]GGATACTATTGCATT	2177
rs758298615	snp	C/T	1.65089e-05	0.00287301	intron-variant	FANCD2	GRCh38.p7	3:10073401	GAAGGTTTGTGACAT[C/T]CCAGTGAGATTAACA	2177
rs758299217	in-del	-/ATC			intron-variant	FANCD2	GRCh38.p7	3:10067511	CAACACATTAAAAAT[-/ATC]AGCTGGGCACGAGGT	2177
rs758322537	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10079056	GACCAGCCTGGCCAA[C/T]GTGGCAAGAGCCTGT	2177
rs758334111	snp	C/G	1.70472e-05	0.00291947	intron-variant	FANCD2	GRCh38.p7	3:10043190	ATGTCACAATTTTCT[C/G]ACATCCCACTGTCAG	2177
rs758397626	in-del	-/T	1.65222e-05	0.00287417	intron-variant	FANCD2	GRCh38.p7	3:10052374	TCATTGTTGGCATCA[-/T]TTTTTTCCACAGGGC	2177
rs758443273	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10073651	GAGGTACTTGATTAT[C/T]AGTAGTTCCCTTTTA	2177
rs758443695	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093056	ATGCCATCTTCTCAA[C/T]ACTCCCAGTTGGAAT	2177
rs758446578	snp	A/T	1.64738e-05	0.00286995	synonymous-codon	FANCD2	GRCh38.p7	3:10041653	GAATACTTCACTCAC[A/T]GTCCCAATCCTGGAT	2177
rs758470099	in-del	-/A			utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101571	TTGTATTTTTAGTAG[-/A]TACGGGGTTTTACCA	2177
rs758475123	snp	C/T	1.64822e-05	0.00287068	stop-gained	FANCD2	GRCh38.p7	3:10063831	CATTCCTGCAGTGAG[C/T]AGTCTCCTCAGGCCT	2177
rs758492931	snp	G/T	1.65293e-05	0.00287479	missense	FANCD2	GRCh38.p7	3:10032912	AATGACAGCATCTTT[G/T]TAAAGCTTCTTAAGA	2177
rs758495271	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10075439	ATCACCCGCCTTGGC[A/C]TCCCAAAGTGCTGGG	2177
rs758557877	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10035436	TTAGCCTAATACATC[C/T]GGCGGCCCCATTTAT	2177
rs758567168	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085219	AAAGTAAACCTATGG[C/T]CCAGGCGTGGTGGCT	2177
rs758574242	snp	A/C	1.64798e-05	0.00287047	intron-variant	FANCD2	GRCh38.p7	3:10063767	GGCAGCCCAAGGTTT[A/C]AACCATTCTTCCTCT	2177
rs758579639	snp	A/G	1.67161e-05	0.00289098	intron-variant	FANCD2	GRCh38.p7	3:10033002	TAATTTTATTCTCTG[A/G]GTTTAATGAAATAGT	2177
rs758616472	snp	A/T	1.65674e-05	0.00287809	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081054	CCCTTAGTTTCTGAG[A/T]CGCTATCCAGCAGTT	2177
rs758625993	snp	G/T	1.6477e-05	0.00287024	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085908	ACACAGCCAGCCTTT[G/T]GAGGAACTACTCAGG	2177
rs758626050	snp	A/G	1.6473e-05	0.00286988	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094274	TAGAGGTAACAGTGT[A/G]TCTCTCTTCTTCAGT	2177
rs758628578	snp	C/T	1.66327e-05	0.00288376	missense	FANCD2	GRCh38.p7	3:10065870	CTCTCTCAGATTGTC[C/T]TATATTCCTAACTGA	2177
rs758652840	snp	A/C			utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101488	TCTCCTAGGTTCAAG[A/C]GATTCTCCTGCCTCA	2177
rs758678240	in-del	-/T	0.244898	0.249948	intron-variant	FANCD2	GRCh38.p7	3:10073238	TGAGTCACTTTTCTC[-/T]TTTTAATATAAAAGA	2177
rs758697688	in-del	-/A	1.64738e-05	0.00286995	frameshift-variant	FANCD2	GRCh38.p7	3:10064390	TCTGTAATGATTTCC[-/A]GGATGCCTTCGTAGT	2177
rs758718558	snp	A/G	0.000152502	0.00873086	missense	FANCD2	GRCh38.p7	3:10065966	TATTTCTTACTCTCA[A/G]CTGGTTCCGAGAGGT	2177
rs758739775	snp	A/G	1.6476e-05	0.00287014	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088424	GTTCCCATATGTAAG[A/G]TTCCTTTGTCTTCTT	2177
rs758739942	snp	A/G	1.66095e-05	0.00288175	intron-variant	FANCD2	GRCh38.p7	3:10046563	TTTTTCTGTTGTTGC[A/G]TATTTATTGACAATA	2177
rs758749466	snp	C/T	6.59207e-05	0.00574073	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088531	TAATGACCAGCTCCA[C/T]GCTCTGCTCTGGTGA	2177
rs758751922	snp	A/G	3.45775e-05	0.00415783	intron-variant	FANCD2	GRCh38.p7	3:10043874	CACAAGGTAATGTTC[A/G]TGTACTATGCATTTT	2177
rs758768583	snp	G/T			upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10026003	CTTGTCCAAGGTCAC[G/T]GCGGTGTGAGGTAGG	2177
rs758768787	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084062	GCAGTGGCGCGATCT[C/T]GGCTCACTATAACCT	2177
rs758781334	in-del	-/CAT	1.65012e-05	0.00287234	cds-indel	FANCD2	GRCh38.p7	3:10074555	GGAAGGAAGAAAAGA[-/CAT]CATTGTTACTACATA	2177
rs758809407	in-del	-/T	1.65074e-05	0.00287288	intron-variant	FANCD2	GRCh38.p7	3:10034544	ATCCCAAAGTATGTA[-/T]TTTTCCCCTGGTATT	2177
rs758843847	snp	A/G	3.29484e-05	0.00405871	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096393	TGGAACTTTTAGTTT[A/G]CAGAGTCAAAGCTAT	2177
rs758851677	snp	C/G			upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026323	GAACTCTGCTGCAGC[C/G]GTGAGCCCAGCTTAT	2177
rs758924373	snp	C/T	1.64732e-05	0.0028699	intron-variant	FANCD2	GRCh38.p7	3:10064705	TCCTGAGCTGCAACA[C/T]CAGATTCTGGTTTTT	2177
rs758938391	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10032144	GCCACTGTGCTGGGT[C/T]GGAAATATGCATTTT	2177
rs758972512	in-del	-/ATCCTCACACAGG	5.03339e-05	0.00501641	intron-variant	FANCD2	GRCh38.p7	3:10043162	CAAGGTAAAGAGCTC[-/ATCCTCACACAGG]ATGTCACAATTTTCT	2177
rs758980826	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10030372	AAAGTGCTGGGATAT[C/T]GGACGTGAGCCACCA	2177
rs758983789	snp	C/G	1.65293e-05	0.00287479	missense	FANCD2	GRCh38.p7	3:10032888	CATATTGCTAATGAA[C/G]TTGAAGAAAATGACA	2177
rs759015869	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10058278	TCTTACCTTTCTCAG[C/T]ATCACCCATATATAA	2177
rs759019069	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10043025	GAATGAGCAGAAAAC[C/T]ATAGCTAATATTTAC	2177
rs759045464	snp	G/T	1.64811e-05	0.00287059	intron-variant	FANCD2	GRCh38.p7	3:10063785	CCATTCTTCCTCTTT[G/T]CTCCAGGTGACCTCC	2177
rs759048793	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10030005	TGGCCAGGGGCTGTC[C/T]GGAACTCCTGACCTC	2177
rs759061683	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10080982	CTTAGGTTAACAACT[C/T]ATTTCTCCCATCTGC	2177
rs759072117	in-del	-/TG	3.29511e-05	0.00405887	intron-variant	FANCD2	GRCh38.p7	3:10035241	TACTGCAGGTAAGAC[-/TG]TCACTTTTTCTGTGA	2177
rs759080799	in-del	-/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095879	GGTCCTGAACAGTGA[-/T]TTTTTTTTTTTTTTT	2177
rs759101076	snp	A/G	1.66167e-05	0.00288237	intron-variant	FANCD2	GRCh38.p7	3:10039897	AGCTATGGGGGTTCT[A/G]TCACTGCAGTATGCA	2177
rs759141106	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10069012	TTATAGACTTAAATC[G/T]AAGACTTCAAATTAT	2177
rs759189761	snp	C/G	1.64931e-05	0.00287163	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085941	AGTCATAACTACATA[C/G]CCAAGATTGTTGTCC	2177
rs759198130	snp	C/T	3.30213e-05	0.00406319	missense	FANCD2	GRCh38.p7	3:10065921	TGGAGTCCATGTCTG[C/T]TAAAGAGCGTTCATT	2177
rs759199525	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10067523	AATATCAGCTGGGCA[C/T]GAGGTGGCTCACGCC	2177
rs759252565	snp	C/T	1.64749e-05	0.00287005	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085872	CCTCCATGTCCTTAG[C/T]AGCCGACTGAAACAG	2177
rs759280640	snp	A/G	3.29625e-05	0.00405958	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093320	TCTGCATGTATGTTT[A/G]AAGGTGAGAGATTTA	2177
rs759287831	snp	C/T	1.78541e-05	0.00298776	intron-variant	FANCD2	GRCh38.p7	3:10043910	TTGCAGACTTAAAAG[C/T]AATGACATTGGCTAG	2177
rs759308509	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10074446	GCATTAAATAAATGC[A/G]TATTTGTACTTTGAA	2177
rs759314164	snp	A/G	6.75973e-05	0.00581327	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087302	TTTTTTTTTTTTTTA[A/G]TGAATAGGACTAATA	2177
rs759322162	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10058195	GAGACCGTGGAGATT[A/T]GGCCCACTCTTGTGC	2177
rs759324309	snp	C/T	1.66932e-05	0.002889	intron-variant	FANCD2	GRCh38.p7	3:10043823	GACTCTCTCCTGTTT[C/T]TTCAGGCAATTGAAA	2177
rs759348779	snp	C/T	4.94197e-05	0.00497066	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088475	AGACAATTCCTCTGT[C/T]GGGTGTGGCCAAGTG	2177
rs759350940	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10053664	ATTTCCTAGTGTGTA[A/G]TAGTGGAAATGGAGT	2177
rs759354462	snp	G/T	1.64841e-05	0.00287085	missense	FANCD2	GRCh38.p7	3:10052422	TAACATATCCCCTCA[G/T]CAAATACGAAAACTC	2177
rs759396763	snp	A/C/G	3.29996e-05	0.00406189	synonymous-codon	FANCD2	GRCh38.p7	3:10073335	AGAATGTGACCCTAC[A/C/G]CCATCTCATAGAGGC	2177
rs759485235	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093515	AGCCAGTTTTCCTAT[A/G]AATTTGAAAACTTTT	2177
rs759494923	snp	A/T	1.64901e-05	0.00287137	intron-variant	FANCD2	GRCh38.p7	3:10074681	ACACTGAAGTAAGTG[A/T]CAGGCTAGGATCTCA	2177
rs759497897	snp	A/G	1.64795e-05	0.00287045	missense	FANCD2	GRCh38.p7	3:10035176	TTTTTTTTACAGTAT[A/G]GGTGCATCTTATTCT	2177
rs759516610	snp	A/T	1.6473e-05	0.00286988	missense, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10081449	TGCTGCAGATTTTTC[A/T]TGGGCTTTTTGCTTG	2177
rs759546582	snp	A/G	1.64928e-05	0.00287161	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101188	TTCTTTGCCCCTTAG[A/G]ATGGTGAAGAAGACG	2177
rs759550499	snp	A/G	1.66749e-05	0.00288741	intron-variant	FANCD2	GRCh38.p7	3:10049542	CTTTAGATATTGAAT[A/G]CTATAATTGGTGGGA	2177
rs759557989	snp	C/T	1.64735e-05	0.00286993	synonymous-codon	FANCD2	GRCh38.p7	3:10042606	TATTAGATTGGAGGA[C/T]TTACCTGTGATAATA	2177
rs759595536	in-del	-/TC	0.000280512	0.0118397	intron-variant	FANCD2	GRCh38.p7	3:10073226	TATTAATTACTTGAG[-/TC]TCACTTTTCTCTTTT	2177
rs759627996	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10046211	GGTGCATGCTGCCAC[A/G]CCCGGCTAATTTTTT	2177
rs759630093	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10066154	CTTAGGTAGCCAAAT[C/G]AGAATACTTAGAATT	2177
rs759639388	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10035331	TAGAGTAGGGTTAAT[C/T]GGAGAATTTGGGTTT	2177
rs759654852	snp	C/T	9.93904e-05	0.00704878	intron-variant	FANCD2	GRCh38.p7	3:10064317	GCTGTACAGCAAGTA[C/T]ACTCTGCACTGCCCT	2177
rs759656108	snp	C/T			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027405	AGATGAAAAGAACAC[C/T]TTTGTGCAAAGGCAC	2177
rs759686612	snp	A/G	1.67413e-05	0.00289316	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095263	CTTCATCACCTGTGT[A/G]GGCATTCCAAGGTAA	2177
rs759710769	snp	G/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098452	GAGTCACCAATACAG[G/T]CTAGCCTTTTAAAAT	2177
rs759718454	snp	A/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097356	TAGGAGACTGGAGTT[A/T]ATTTCACCTCTGCAG	2177
rs759732362	snp	G/T	1.64787e-05	0.00287038	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10081333	ACTGTCCTAAAATCA[G/T]TTTTATTTTTAGTGT	2177
rs759743690	snp	A/G	1.64735e-05	0.00286993	missense	FANCD2	GRCh38.p7	3:10064404	CAGGATGCCTTCGTA[A/G]TGGACTCCTGTGTTG	2177
rs759752175	snp	C/G/T	8.23955e-05	0.00641811	intron-variant	FANCD2	GRCh38.p7	3:10042528	GTAGTGACATGAAAA[C/G/T]CTATTAAGTTTCTGT	2177
rs759753951	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10065372	ATGAAGTGTGGTCTA[C/G]AAATTTATTTCTCCT	2177
rs759789445	in-del	-/GGAGT			intron-variant	FANCD2	GRCh38.p7	3:10051414	AAAAAAAAACAAAAA[-/GGAGT]GAGGGATTTATCTCC	2177
rs759828462	in-del	-/AAA			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10028051	AACCCTGTCTCTACT[-/AAA]AAAAAAAAAAAAAAA	2177
rs759860839	snp	C/T	1.64741e-05	0.00286998	intron-variant, stop-gained	FANCD2, FANCD2OS	GRCh38.p7	3:10098915	ACTTATGTTTATTGT[C/T]AAATGCTTCTATGCC	2177
rs759868001	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10050010	GGAGAATAGGATATA[C/T]ATGGAGAGGAATGAT	2177
rs759874296	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10056357	TGGAATTGCTGGATC[A/G]TATGATGACCATATG	2177
rs759878503	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10089552	TCAGCTCACTGCAAC[C/T]TCCACCTCCTGGGTT	2177
rs759916810	snp	A/T	1.87362e-05	0.00306068	intron-variant	FANCD2	GRCh38.p7	3:10039406	GAGTATGTTTCTCAT[A/T]TCTTTTGGAGGTTGT	2177
rs759927900	in-del	-/A	0.000133409	0.00816619	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101155	CCAGAGCAGTAACCT[-/A]AAATGCTTATTTATT	2177
rs759942234	snp	C/T	1.65356e-05	0.00287533	synonymous-codon	FANCD2	GRCh38.p7	3:10046702	ACAGCTGCTCCAGAG[C/T]ACATTCTCTGTTCAT	2177
rs759943664	snp	C/T	1.65477e-05	0.00287638	missense	FANCD2	GRCh38.p7	3:10043530	AGCTGTATTATTCTC[C/T]TCTTTGATGTAATAA	2177
rs759948329	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10038211	TGGCCAGGCTGGCCT[C/G]GAACTCCTGACCTCA	2177
rs760042942	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10078021	CAAAAAAGAAAGAAA[A/G]AAAATTATCATGAAA	2177
rs760054667	snp	C/G			upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026147	ATGGGTAGGACCACC[C/G]AGAGGCAGATGTTGG	2177
rs760054945	snp	C/T	1.6593e-05	0.00288031	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090316	TGTTGTTTTCTTCCG[C/T]GTGATGATGGCTGAA	2177
rs760111133	snp	C/T	1.74983e-05	0.00295784	intron-variant	FANCD2	GRCh38.p7	3:10039260	CTCAGTTCCCTGTTT[C/T]CTCTTCCTAACATTT	2177
rs760164822	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10058004	TTTTTGAGTTAAGCT[A/G]TCAAGTTTGCCCTTT	2177
rs760167204	in-del	-/TTTTC	1.66203e-05	0.00288268	frameshift-variant	FANCD2	GRCh38.p7	3:10049484	CCATCTGCTATGATG[-/TTTTC]ATGAATGCTGTCTTT	2177
rs760167962	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10059279	TCAGCCTCCCAAAGT[A/G]TTAGGATGACAGGTA	2177
rs760178197	snp	A/G	1.65496e-05	0.00287655	intron-variant	FANCD2	GRCh38.p7	3:10048096	GGGAACACAGAAAGG[A/G]AAAATAATCTGATGT	2177
rs760232361	in-del	-/ACTA			intron-variant	FANCD2	GRCh38.p7	3:10047865	ACTCTTAGGTTGTGT[-/ACTA]ACTAACTGTTTCCTA	2177
rs760246372	snp	C/T	1.64757e-05	0.00287012	missense	FANCD2	GRCh38.p7	3:10048038	TTAAGTTTTTTGACA[C/T]GTACTGCCAGCAGGT	2177
rs760269699	snp	A/G	1.70638e-05	0.00292089	intron-variant	FANCD2	GRCh38.p7	3:10043451	TTTTCTGGTACGTAG[A/G]AGAGTAATTTTTTTC	2177
rs760271214	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10079785	TATACAGTGTACAAA[C/T]GTGCACCTAGCATCC	2177
rs760296624	snp	C/T	3.295e-05	0.00405881	synonymous-codon	FANCD2	GRCh38.p7	3:10064792	CACTCAGGATGGGAT[C/T]GCCATAAACCTCCTG	2177
rs760324486	snp	C/G	1.64814e-05	0.00287061	missense	FANCD2	GRCh38.p7	3:10063876	GATGAATTTGCCAAC[C/G]TGATCCAACATGAAA	2177
rs760325562	snp	G/T	0.000100626	0.00709244	intron-variant	FANCD2	GRCh38.p7	3:10074521	TTTGTTGCTGTGACT[G/T]CCCCATAGGAGTTCA	2177
rs760361533	in-del	-/TAT	3.3106e-05	0.0040684	cds-indel	FANCD2	GRCh38.p7	3:10043520	CAGCGGTCAGAGCTG[-/TAT]TATTCTCCTCTTTGA	2177
rs760374605	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10029817	GAGACGGAGTCTCAC[C/T]CTGTCACCCAGGCTG	2177
rs760427946	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10042143	CCTTGTTTTCCACCC[A/C]CCTCGGCCTCCCAAA	2177
rs760428640	snp	C/T	4.96841e-05	0.00498393	missense	FANCD2	GRCh38.p7	3:10065939	AAGAGCGTTCATTCA[C/T]GTGTTCTCTCATATT	2177
rs760436877	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084719	TTTGTTGAAAGGAAG[A/G]ATGACTATCACTGGT	2177
rs760450030	snp	A/G	1.65277e-05	0.00287464	missense	FANCD2	GRCh38.p7	3:10032906	GAAGAAAATGACAGC[A/G]TCTTTGTAAAGCTTC	2177
rs760459142	snp	C/G	3.29468e-05	0.00405861	missense	FANCD2	GRCh38.p7	3:10078129	CTGCTTTTCTTGCTG[C/G]AAGATCTCTCCCAGA	2177
rs760464202	snp	A/G	1.67022e-05	0.00288978	intron-variant	FANCD2	GRCh38.p7	3:10039912	ATCACTGCAGTATGC[A/G]AAGAGCAGTAGTAAT	2177
rs760516842	snp	C/T	0.000115374	0.0075943	missense	FANCD2	GRCh38.p7	3:10063799	TGCTCCAGGTGACCT[C/T]CTTGTTGCAGTTGGT	2177
rs760519038	snp	C/T	2.00122e-05	0.00316318	intron-variant	FANCD2	GRCh38.p7	3:10066011	GGATGTTTCACTTAT[C/T]GTGCATAGTTTTTCT	2177
rs760551106	snp	A/G			missense	FANCD2	GRCh38.p7	3:10035178	TTTTTTACAGTATGG[A/G]TGCATCTTATTCTAA	2177
rs760551996	snp	A/G	1.65269e-05	0.00287457	missense	FANCD2	GRCh38.p7	3:10032901	AAGTTGAAGAAAATG[A/G]CAGCATCTTTGTAAA	2177
rs760574880	snp	C/T	3.29516e-05	0.00405891	missense	FANCD2	GRCh38.p7	3:10041631	TTCACAGTGACCTAC[C/T]GATAGAGAATACTTC	2177
rs760582486	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083685	TGAGGTCAGGAGATC[A/G]AGACCGTCCTGGCTA	2177
rs760588840	snp	C/T	1.64757e-05	0.00287012	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088782	GAATCTGTAGTTGTA[C/T]TCTACTTTGTTAATT	2177
rs760762211	snp	A/G	1.64841e-05	0.00287085	missense	FANCD2	GRCh38.p7	3:10036290	CTTCTTTTTTAGCCT[A/G]CCATTATCAAAACCT	2177
rs760766386	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10057514	GGACTAGGGGCATGC[A/G]CCACAACGCCCAGTT	2177
rs760792708	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10039469	CTTTTCCATCCATCC[A/G]TTAGCTTTTTCCAAT	2177
rs760793558	snp	C/G	1.6743e-05	0.0028933	intron-variant	FANCD2	GRCh38.p7	3:10049555	ATACTATAATTGGTG[C/G]GAGGTGGTGGGAAGG	2177
rs760800033	snp	A/G	4.94637e-05	0.00497287	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096340	GATTCACCAGGACAC[A/G]AGACTCACCCAACAT	2177
rs760823688	snp	G/T	1.64738e-05	0.00286995	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088495	GTGGCCAAGTGGGGA[G/T]AAAGAGAAGAGCAAC	2177
rs760825205	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097201	CCGCAGGACCGAGGC[A/G]AAATTGAAATTGCTA	2177
rs760838620	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10077130	CCCAGCTACCTGGGC[A/G]GCTGAGGTGGGACCA	2177
rs760840306	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10045329	ACCTGCCACCACGCC[C/T]GGCTAATTTTTTGTA	2177
rs760887535	in-del	-/TCCTGTGTATC			intron-variant	FANCD2	GRCh38.p7	3:10035487	GTTCTTAAAGCTGCA[-/TCCTGTGTATC]TCTGAGTATCTGGTA	2177
rs760895492	snp	A/G	3.5946e-05	0.00423931	intron-variant	FANCD2	GRCh38.p7	3:10047869	CTTAGGTTGTGTACT[A/G]ACTGTTTCCTACAGC	2177
rs760963969	snp	C/G	1.64735e-05	0.00286993	missense	FANCD2	GRCh38.p7	3:10064414	TCGTAGTGGACTCCT[C/G]TGTTGTTCCGGAAGG	2177
rs760970277	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10054991	ACAGGGGCAATCACT[G/T]TATAAGCTTCTGAGA	2177
rs760981756	snp	G/T	1.64735e-05	0.00286993	missense	FANCD2	GRCh38.p7	3:10042614	TGGAGGATTTACCTG[G/T]GATAATAAAGTTCAT	2177
rs760997218	snp	G/T	1.64743e-05	0.00287	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092132	GGGAATACAGTAAGG[G/T]AAGTATTTGGCTGTG	2177
rs761002381	snp	A/C			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100617	CCTCAGATGATCTAC[A/C]CACCTCAGCCTTCCA	2177
rs761006502	snp	C/G	1.67295e-05	0.00289214	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101145	CAGAGGTCACCCAGA[C/G]CAGTAACCTAAAATG	2177
rs761008297	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10068669	TTATATAGAACCACC[A/G]AAGACCCAGAATAGC	2177
rs761074497	snp	C/G	1.66535e-05	0.00288556	splice-donor-variant	FANCD2	GRCh38.p7	3:10062212	GAGCAGTGCACACAG[C/G]TGAGTTCTTTTTTTC	2177
rs761089162	snp	A/T	1.6596e-05	0.00288058	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090321	TTTTCTTCCGTGTGA[A/T]GATGGCTGAACTAGA	2177
rs761151603	snp	A/T	1.64985e-05	0.0028721	intron-variant	FANCD2	GRCh38.p7	3:10028734	CCAGTAAGTATCTAG[A/T]CATTTGTTGCTTTAT	2177
rs761167211	snp	C/T	1.67744e-05	0.00289602	intron-variant	FANCD2	GRCh38.p7	3:10072833	AATGGTGGTGTGTAA[C/T]TGGTACACATTGAGC	2177
rs761199690	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10037972	TTTTTTCAGAGTCCT[A/G]ATACAGTAATAGTAA	2177
rs761211339	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10075850	ATTATCCTGCCTCAG[C/T]CTCCCAAGTAGCTGG	2177
rs761223784	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10068900	CATTGGGGAAAGACA[C/G]TCTCTTCAATAAATG	2177
rs761258624	snp	A/G	1.65444e-05	0.00287609	synonymous-codon	FANCD2	GRCh38.p7	3:10043541	TCTCCTCTTTGATGT[A/G]ATAAAGTCAGCTATT	2177
rs761298529	snp	C/T	1.64738e-05	0.00286995	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087176	CCATCAAAGCATTCC[C/T]AGTTTCCAGTGTGCT	2177
rs761350443	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10056763	GTTTGATTTGCATTT[G/T]CTAATGACTAATGAT	2177
rs761352961	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10032640	TTCTTCAAATGAAAA[C/T]AGGTGAAAATAATTC	2177
rs761374612	snp	A/T	4.97179e-05	0.00498562	intron-variant	FANCD2	GRCh38.p7	3:10064886	CAAAAGTCAGTATAG[A/T]TTTTCTTTTCTAAAC	2177
rs761393012	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10072700	CTGTGTTATCTCTGG[C/T]CATTTTGCTATGCCA	2177
rs761411799	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10074359	CCCATCTTAAATTAG[A/G]TGCTCTGTCTTGGGA	2177
rs761454449	snp	C/T	1.67882e-05	0.00289721	intron-variant	FANCD2	GRCh38.p7	3:10043467	AGAGTAATTTTTTTC[C/T]TCTCTGCTACTTGTA	2177
rs761454597	snp	A/G	3.29451e-05	0.00405851	missense	FANCD2	GRCh38.p7	3:10049425	GGGAATGAAGCTGAA[A/G]TTGATACTGCCTTAG	2177
rs761465333	snp	C/T	1.6473e-05	0.00286988	synonymous-codon	FANCD2	GRCh38.p7	3:10065403	TCTCAGATTGGTGTC[C/T]CCGCTGTGCCTGGCT	2177
rs761479186	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096903	TTGGGGGACCTGCCC[C/T]GATAATCACGTAGGT	2177
rs761548048	in-del	-/TCCCACC	1.66751e-05	0.00288744	intron-variant	FANCD2	GRCh38.p7	3:10049541	CTTTAGATATTGAAT[-/TCCCACC]ACTATAATTGGTGGG	2177
rs761562459	snp	A/G	1.65064e-05	0.00287279	intron-variant	FANCD2	GRCh38.p7	3:10063944	TTCTTAAAGCAATAA[A/G]GCATGAGAGCTGCTT	2177
rs761571860	in-del	-/GTC	1.95433e-05	0.0031259	intron-variant	FANCD2	GRCh38.p7	3:10062245	TTCTTTCTTTTTCCT[-/GTC]TTTTTTTTTTTTTTA	2177
rs761582104	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10047345	TTTCATTGCATTTTC[C/T]CCAATAAAGCATTAT	2177
rs761591272	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10057703	ACCATCTTTGTGAAA[A/T]GTTGAACATTACTAA	2177
rs761607026	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100898	AATGTGGAGAAACCC[C/T]GTCTCTACCAAAATA	2177
rs761632348	snp	A/G	1.64833e-05	0.00287078	intron-variant	FANCD2	GRCh38.p7	3:10042511	TTCAGTACAAAGTTG[A/G]GGTAGTGACATGAAA	2177
rs761633215	snp	C/T	1.64838e-05	0.00287083	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093362	TTCATATTTATTCTT[C/T]CTGTGGATCACTCTA	2177
rs761634079	snp	A/C	1.66918e-05	0.00288888	intron-variant	FANCD2	GRCh38.p7	3:10032994	TTTTAATCTAATTTT[A/C]TTCTCTGGGTTTAAT	2177
rs761639254	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082351	TCCCATTATCTCTCA[A/G]CCTGGACTGGGCTAG	2177
rs761648908	snp	C/T	1.68213e-05	0.00290006	intron-variant	FANCD2	GRCh38.p7	3:10049331	TTTAGAATGGCCATC[C/T]ATATTTTGTTTTACA	2177
rs761722300	snp	A/G	1.64966e-05	0.00287194	synonymous-codon	FANCD2	GRCh38.p7	3:10034479	CATAGCTGTGGATCA[A/G]ATAGCTTTCCAAAAG	2177
rs761727308	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10062912	CGCTATGTTGACCAG[C/G]CTGGTCTCAAACTCC	2177
rs761727385	snp	A/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095581	GGTAACAGGACTGTG[A/T]TGTAAGTGATGATCC	2177
rs761739960	in-del	-/GGC	1.65589e-05	0.00287736	cds-indel	FANCD2	GRCh38.p7	3:10073273	AAACAAAAAACAGAT[-/GGC]AGCAAGACATCCTCC	2177
rs761754388	snp	A/T	1.78493e-05	0.00298736	intron-variant	FANCD2	GRCh38.p7	3:10052543	TTTTTTTTGAGACAG[A/T]GTCTAGCTCTGTCTC	2177
rs761774965	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10075626	TGAGATGGGATTTCA[C/T]CAGAGAGTAGAATTT	2177
rs761797072	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10037888	GATACACACATACAC[A/T]TATGTATATTAATAG	2177
rs761800436	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10034253	TCATTTGAACCCAGG[A/G]GGCGGAAGTTCCTGT	2177
rs761825171	snp	A/G	2.12362e-05	0.00325847	intron-variant	FANCD2	GRCh38.p7	3:10066019	CACTTATTGTGCATA[A/G]TTTTTCTCAAAACTA	2177
rs761826377	snp	G/T	1.64749e-05	0.00287005	missense	FANCD2	GRCh38.p7	3:10041638	TGACCTACTGATAGA[G/T]AATACTTCACTCACT	2177
rs761842101	snp	A/G	3.29516e-05	0.00405891	missense	FANCD2	GRCh38.p7	3:10046620	TCATCTATAGCACCA[A/G]TACTCAGACAAAGAA	2177
rs761933065	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10054272	CATAACTTGTAACTC[A/G]TTTGTAGCTTTAGTG	2177
rs761955186	snp	A/C/T	3.29491e-05	0.00405877	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088797	TTCTACTTTGTTAAT[A/C/T]AGTGGGTCAAATATT	2177
rs761980909	in-del	-/TT	0.294078	0.246084	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087282	GATGGGCCTAGATCC[-/TT]TTTTTTTTTTTTTTT	2177
rs761994012	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10039082	TTAGCATGTCTTCTA[A/G]ACATTTTTCTTAACA	2177
rs762013605	snp	C/T	1.87915e-05	0.00306519	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098683	CCCTAAATGTGATCA[C/T]TATAACCCACCATTT	2177
rs762049274	snp	C/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088026	CACATCAGAAAGCAA[C/G]ATAAAAATGCAAAAC	2177
rs762054113	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10076905	TACAGGTGCCCACCA[C/T]CACATCAGCTAATTT	2177
rs762059623	snp	A/G	1.64863e-05	0.00287104	synonymous-codon, downstream-variant-500B	FANCD2, FANCD2OS	GRCh38.p7	3:10081129	GAATATTGGATTCTC[A/G]CATCTCCAACAGAGA	2177
rs762060936	snp	A/G	1.64732e-05	0.0028699	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085848	AAATCAGAATTTACT[A/G]TATTCAGCCCTCCAT	2177
rs762070869	snp	C/T	1.64846e-05	0.0028709	synonymous-codon	FANCD2	GRCh38.p7	3:10036304	TGCCATTATCAAAAC[C/T]TTATTTGAGAAGTTG	2177
rs762109767	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10067400	CCCTGATACCAAAAC[C/G]AGACAAAGACACATC	2177
rs762114353	snp	G/T	1.64762e-05	0.00287016	intron-variant	FANCD2	GRCh38.p7	3:10035241	TACTGCAGGTAAGAC[G/T]GTCACTTTTTCTGTG	2177
rs762134211	snp	A/G	2.12199e-05	0.00325723	intron-variant	FANCD2	GRCh38.p7	3:10073017	TTGTCTTGTGTCTCT[A/G]AATAAGCTTCATTGA	2177
rs762147303	snp	A/G	1.64727e-05	0.00286986	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088940	TCCTCCACATTCCCT[A/G]CACTGACCAGGTAAG	2177
rs762148969	snp	A/G	1.64863e-05	0.00287104	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092251	TCATCAACTTGATAA[A/G]GGTGAGTATGGAGAC	2177
rs762149344	snp	A/G	1.64792e-05	0.00287042	intron-variant	FANCD2	GRCh38.p7	3:10078246	AGTGGATTTGGGAAC[A/G]AAGGAGGTATTATGA	2177
rs762172462	in-del	-/TTT			intron-variant	FANCD2	GRCh38.p7	3:10040708	ATTGTACTAGAAGTA[-/TTT]TTTTTAAATTCAGTT	2177
rs762191428	in-del	-/A			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10089285	GCGAAACTCCATCTC[-/A]AAAAAAAAAAAGAAT	2177
rs762224196	snp	C/T	1.64732e-05	0.0028699	intron-variant	FANCD2	GRCh38.p7	3:10064700	CGTATTCCTGAGCTG[C/T]AACATCAGATTCTGG	2177
rs762232434	snp	C/T	3.295e-05	0.00405881	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096386	AAGACCCTGGAACTT[C/T]TAGTTTGCAGAGTCA	2177
rs762234241	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10066630	ACAGTAAGTAGCAGT[A/G]TAGAACTTGTTTCAC	2177
rs762268512	snp	A/G	4.98062e-05	0.00499005	synonymous-codon	FANCD2	GRCh38.p7	3:10043145	GAAAAGTAAAGGACG[A/G]GCAAGGTAAAGAGCT	2177
rs762271650	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10063173	GGCACGGTGGTTTGC[A/G]ATTGTAATCCTAGCA	2177
rs762278011	in-del	-/CTT	7.05393e-05	0.00593841	intron-variant	FANCD2	GRCh38.p7	3:10034689	TATTTTTTAAATCTC[-/CTT]AAGATAATAGAAGAA	2177
rs762305332	snp	A/C	3.29582e-05	0.00405931	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10081495	GTGTGGAGAGAACTG[A/C]GTATATACTTGCTTT	2177
rs762330444	snp	C/T	1.66363e-05	0.00288407	intron-variant	FANCD2	GRCh38.p7	3:10072855	ACATTGAGCTTCAGC[C/T]TGCTGTTTGTTTCAG	2177
rs762344233	in-del	-/TCTT			intron-variant	FANCD2	GRCh38.p7	3:10041841	CACATTTGATATCTC[-/TCTT]TTTTTTTTTTTTTCC	2177
rs762381442	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10041211	TCTCAAAAAACAAAC[A/G]AACAAAAAAAAAAGC	2177
rs762381604	snp	C/T	1.64746e-05	0.00287002	missense	FANCD2	GRCh38.p7	3:10039770	TTGCTCCAGAGAACC[C/T]GCAGCATGACATCAT	2177
rs762406982	snp	C/T	1.64738e-05	0.00286995	stop-gained	FANCD2	GRCh38.p7	3:10047956	ATTCTGTCGCTGGCT[C/T]AGAGTTTGCTTCACT	2177
rs762474774	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10068864	AATGAACTCATTCTC[A/G]GCAAAGGTGCCAAGA	2177
rs762515174	snp	C/T	3.33611e-05	0.00408405	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101153	ACCCAGAGCAGTAAC[C/T]TAAAATGCTTATTTA	2177
rs762526976	snp	G/T	3.29462e-05	0.00405857	missense	FANCD2	GRCh38.p7	3:10065408	GATTGGTGTCTCCGC[G/T]GTGCCTGGCTCCGTA	2177
rs762544228	in-del	-/A			frameshift-variant	FANCD2	GRCh38.p7	3:10073307	CTGACACACTTTCAG[-/A]AGAGAAAAATTCAGA	2177
rs762544551	snp	A/T	1.65701e-05	0.00287833	intron-variant	FANCD2	GRCh38.p7	3:10028764	TTTCCTGTAGCAATG[A/T]GTGAGGCATGTGAGA	2177
rs762600757	snp	C/T	1.80892e-05	0.00300737	intron-variant	FANCD2	GRCh38.p7	3:10062240	TTCCTTTCTTTCTTT[C/T]TCCTGTCTTTTTTTT	2177
rs762604718	snp	A/G	1.6489e-05	0.00287128	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10098967	AGCTTCTGTGCTTAT[A/G]TAATTTTTGGGACCC	2177
rs762610301	snp	C/G/T	3.29464e-05	0.00405861	missense	FANCD2	GRCh38.p7	3:10064396	ATGATTTCCAGGATG[C/G/T]CTTCGTAGTGGACTC	2177
rs762620814	snp	A/C			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082324	GTCCCTGTTTCTCCA[A/C]TGCTTCCAGACTCCC	2177
rs762634435	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10055168	AATTTTGATAAAATA[C/T]ACATAATATAAAATA	2177
rs762640786	in-del	-/TT			intron-variant	FANCD2	GRCh38.p7	3:10062248	TTTCTTTTTCCTGTC[-/TT]TTTTTTTTTTTTAGA	2177
rs762676876	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10060897	TGCCATTACAAACCG[A/G]CATTGGATTTCAGTT	2177
rs762681457	snp	C/T	3.29473e-05	0.00405864	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092157	GCTGTGACTCAGAGG[C/T]GCCCATATATTTGGC	2177
rs762683227	snp	A/G	1.64749e-05	0.00287005	missense	FANCD2	GRCh38.p7	3:10078090	TGACAGGCTACAGAA[A/G]TTGTGCAACTTGGGC	2177
rs762698137	snp	C/T	6.65912e-05	0.00576985	intron-variant	FANCD2	GRCh38.p7	3:10049530	TGGCTTCTTGTACTT[C/T]AGATATTGAATACTA	2177
rs762705166	snp	C/T	1.64738e-05	0.00286995	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087191	CAGTTTCCAGTGTGC[C/T]CTTTATCTCATCAGA	2177
rs762706688	snp	C/T	3.33311e-05	0.00408221	utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101304	TGTGTCTCTGCCAGC[C/T]TGTGATCATTTTGTG	2177
rs762714221	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10072338	GGCTGGAGTGTGGTG[A/G]TGCGATCTCTGCTTA	2177
rs762724830	snp	G/T	1.64789e-05	0.0028704	stop-gained	FANCD2	GRCh38.p7	3:10074659	TTCATCTTAGATACT[G/T]AAATGCACACTGAAG	2177
rs762740183	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10053987	AGGCCAAGGCAGGCG[A/T]ATCACATGTGCCCTG	2177
rs762740358	snp	G/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082467	ATTTTGATTTCTGAT[G/T]GCTCTTAGATTTTTC	2177
rs762742734	snp	A/G	1.71117e-05	0.00292499	intron-variant	FANCD2	GRCh38.p7	3:10034684	TTTTTTATTTTTTAA[A/G]TCTCCTTAAGATAAT	2177
rs762760914	snp	C/T	1.64743e-05	0.00287	missense	FANCD2	GRCh38.p7	3:10049438	AAGTTGATACTGCCT[C/T]AGATGTCCTTCTAGA	2177
rs762765583	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10031840	ACTCTGGTATATGGC[A/T]TGGAATATGCCTTTT	2177
rs762778755	snp	A/G	1.65477e-05	0.00287638	synonymous-codon	FANCD2	GRCh38.p7	3:10043565	AGCTATTAGATATGA[A/G]AAAACCATTTCAGAA	2177
rs762788048	snp	G/T	1.64917e-05	0.00287151	missense	FANCD2	GRCh38.p7	3:10034499	CTTTCCAAAAGAAGC[G/T]CTTTCAGACCCTGAG	2177
rs762793040	snp	A/C/G	6.59254e-05	0.00574099	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094387	TAAGAGCAGAGAACA[A/C/G]AGATATGCACTGAAG	2177
rs762801379	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10059680	GGTTGGTGGCGGGCA[C/T]CTGTAGTCCCAGCTA	2177
rs762810414	in-del	-/AGGGGAAGG	1.70107e-05	0.00291634	cds-indel	FANCD2	GRCh38.p7	3:10067249	CATCACCTGAGATGA[-/AGGGGAAGG]TGCTCACTCGGTTAA	2177
rs762876564	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10050546	GAGAATGGCGTGAAC[C/T]CAGGAGGCGGAGCTT	2177
rs762898064	snp	C/T	1.77008e-05	0.00297491	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087289	CTAGATCCTTTTTTT[C/T]TTTTTTTTTTTAATG	2177
rs762911249	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086541	TTGTCACCCAGGCTG[A/G]AGTGATCCCAGCTCA	2177
rs762915519	snp	C/T	3.32486e-05	0.00407715	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090300	CTTCTAGGCATACTT[C/T]TGTTGTTTTCTTCCG	2177
rs762926148	snp	A/C			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095551	GGTATATGTTTACTT[A/C]TGCAAAGTCCTCTAG	2177
rs762928348	snp	A/C			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081057	TTAGTTTCTGAGACG[A/C]TATCCAGCAGTTTCT	2177
rs762955909	snp	C/G	1.65861e-05	0.00287972	intron-variant	FANCD2	GRCh38.p7	3:10064310	ATCTAGGGCTGTACA[C/G]CAAGTACACTCTGCA	2177
rs762971430	snp	A/G	4.94694e-05	0.00497316	missense	FANCD2	GRCh38.p7	3:10046689	GCTGCATTCAAGAAC[A/G]GCTGCTCCAGAGTAC	2177
rs762983378	snp	C/G	1.64814e-05	0.00287061	intron-variant	FANCD2	GRCh38.p7	3:10042520	AAGTTGAGGTAGTGA[C/G]ATGAAAACCTATTAA	2177
rs763001544	snp	G/T	1.64817e-05	0.00287064	missense	FANCD2	GRCh38.p7	3:10063893	GATCCAACATGAAAA[G/T]CTGGATCCAAAAGCC	2177
rs763010610	in-del	-/CA	4.96274e-05	0.00498109	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096293	GCATGATGATAAACT[-/CA]CAAAAGATGGATGTT	2177
rs763095281	snp	A/G	1.64814e-05	0.00287061	intron-variant	FANCD2	GRCh38.p7	3:10067169	ACAAGGTTAAAATCT[A/G]AACATTTGGAAGTAT	2177
rs763101310	snp	C/G	1.64822e-05	0.00287068	missense, downstream-variant-500B	FANCD2, FANCD2OS	GRCh38.p7	3:10081146	ATCTCCAACAGAGAT[C/G]TGCCCAAGAAATTGT	2177
rs763153292	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10050293	ATGGCTTAAGAGACA[A/G]TTTGGTGTTAGAATT	2177
rs763159592	snp	A/G	1.64762e-05	0.00287016	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088994	CCTTAAGATAGAATC[A/G]TCATCAGGCTGGGCA	2177
rs763164400	snp	A/T	1.64876e-05	0.00287116	missense	FANCD2	GRCh38.p7	3:10060349	CCGTATTCAAGTACA[A/T]GCTCATTGGGATTAT	2177
rs763177575	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10065556	TGGTAAACTTAGGGA[A/G]AGGGCAGATCAATAC	2177
rs763185403	snp	C/T	3.42067e-05	0.00413548	missense	FANCD2	GRCh38.p7	3:10067266	GGGAAGGTGCTCACT[C/T]GGTTAAAGCACATTG	2177
rs763189891	snp	C/T	0.00162967	0.0284987	synonymous-codon	FANCD2	GRCh38.p7	3:10064774	CGGACTGGAAGAATA[C/T]GACACTCAGGATGGG	2177
rs763226208	snp	C/G			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027580	TTCTACTGGCTAACT[C/G]CTGTTTCAGCCCTCA	2177
rs763231933	snp	C/G	1.64751e-05	0.00287007	missense	FANCD2	GRCh38.p7	3:10046629	GCACCAATACTCAGA[C/G]AAAGAAGTACATTGA	2177
rs763235057	in-del	-/TT			intron-variant	FANCD2	GRCh38.p7	3:10038981	TTTATTAACATTGTC[-/TT]TTTAAAAATTATTAT	2177
rs763281604	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10079525	TCATCAGGCTGATCT[C/T]GAACTCCTGACCTCA	2177
rs763296605	snp	A/C/G	4.9442e-05	0.00497182	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10081323	TACTGAAGCAACTGT[A/C/G]CTAAAATCATTTTTA	2177
rs763311345	in-del	-/GG			intron-variant	FANCD2	GRCh38.p7	3:10034855	TTTTGCCAACTTCAT[-/GG]GGCTGGGGAGGGAGA	2177
rs763323915	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10037148	TTTTTTTTAATTACT[A/G]TGTTAAGAAATGAAC	2177
rs763358836	snp	G/T	3.50551e-05	0.00418645	intron-variant	FANCD2	GRCh38.p7	3:10060256	TCTTTTGCTGTGCCA[G/T]TCCAGCATTTTCATC	2177
rs763377248	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093218	TGTGCTTTGCGCAGC[A/G]GGAAAGAGGCTGGAG	2177
rs763380585	snp	A/G	1.64746e-05	0.00287002	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088808	TAATTAGTGGGTCAA[A/G]TATTTGACTCTCAAT	2177
rs763403740	in-del	-/G	1.65132e-05	0.00287339	frameshift-variant	FANCD2	GRCh38.p7	3:10043066	TAATTTCTGAGCTTC[-/G]GGAGAAGTTGGATCT	2177
rs763444560	snp	C/T	0.000107575	0.00733321	intron-variant	FANCD2	GRCh38.p7	3:10039247	TTGACCAGAAAGGCT[C/T]AGTTCCCTGTTTTCT	2177
rs763486543	snp	A/G	6.82117e-05	0.00583962	intron-variant	FANCD2	GRCh38.p7	3:10043452	TTTCTGGTACGTAGA[A/G]GAGTAATTTTTTTCC	2177
rs763513137	snp	A/C	1.64768e-05	0.00287021	missense	FANCD2	GRCh38.p7	3:10064800	ATGGGATTGCCATAA[A/C]CCTCCTGCCGCTGCT	2177
rs763521354	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10031502	GCAAGACTCCATTTC[A/C]AAAAAAAAAAAAAAA	2177
rs763525147	snp	A/G	1.64806e-05	0.00287054	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098791	TGACATGTCATCCCA[A/G]GCCTCCAAGAGCAAA	2177
rs763530948	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10029287	AGAGGGTCACCTAAA[G/T]CTAGGAGTTCAAGAC	2177
rs763601479	in-del	-/T	0.138458	0.223737	intron-variant	FANCD2	GRCh38.p7	3:10035159	TGGAAAACAGATTTC[-/T]TTTTTTTTTACAGTA	2177
rs763645316	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10038239	TCAAGTGATCTGCTT[G/T]CCTCAGCCCCACAAA	2177
rs763676924	snp	A/G	1.64814e-05	0.00287061	synonymous-codon	FANCD2	GRCh38.p7	3:10063878	TGAATTTGCCAACCT[A/G]ATCCAACATGAAAAG	2177
rs763699692	snp	C/T	1.6563e-05	0.00287771	synonymous-codon	FANCD2	GRCh38.p7	3:10074535	TTCCCCATAGGAGTT[C/T]ACAGGGAAGGAAGAA	2177
rs763702476	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10055351	CCACCCCCTAATAAT[A/C]ACTAATCACATTCTG	2177
rs763711696	snp	C/T	1.64741e-05	0.00286998	intron-variant, missense	FANCD2, FANCD2OS	GRCh38.p7	3:10098832	TATCTCTACAAAACC[C/T]ACCAGAGTCTGGCAC	2177
rs763717076	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10069203	ATAGCAAAGGAAACA[C/T]CAAAGTGAAGAGACA	2177
rs763726507	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10068874	TTCTCAGCAAAGGTG[A/C]CAAGAATATACATTG	2177
rs763730607	snp	A/C	3.30376e-05	0.0040642	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085962	ATTGTTGTCCCAAGA[A/C]ACTCCTAGGAACAGG	2177
rs763731569	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10047035	TGTGGACTTTAGGTG[A/G]TAATTCCTCTAGAAA	2177
rs763733996	in-del	-/TGGA	1.65507e-05	0.00287664	frameshift-variant	FANCD2	GRCh38.p7	3:10043571	AGATATGAGAAAACC[-/TGGA]ATTTCAGAAGCCTGG	2177
rs763750904	snp	G/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098338	CCACCTCACCATACT[G/T]TCCTTTAGCCTCCGC	2177
rs763752397	in-del	-/A	1.66192e-05	0.00288259	intron-variant	FANCD2	GRCh38.p7	3:10049513	TTGTAAAGGTATCTT[-/A]TTGGCTTCTTGTACT	2177
rs763763504	snp	G/T	1.65272e-05	0.0028746	missense	FANCD2	GRCh38.p7	3:10032904	TTGAAGAAAATGACA[G/T]CATCTTTGTAAAGCT	2177
rs763764719	snp	C/T	1.68213e-05	0.00290006	intron-variant	FANCD2	GRCh38.p7	3:10049326	ATCCCTTTAGAATGG[C/T]CATCCATATTTTGTT	2177
rs763801603	snp	C/T	5.06077e-05	0.00503004	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098715	CTTGGTCCATTCACA[C/T]TTAGGGTGAAGAGAT	2177
rs763805447	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088289	AGGGCCAGTGGATCA[A/G]GAACGTGACAGCTTT	2177
rs763829963	in-del	-/TTTCTT			intron-variant	FANCD2	GRCh38.p7	3:10057344	AGTCAAATTTATCTA[-/TTTCTT]TTTCTTTTTCTTTCT	2177
rs763841035	snp	C/T	3.37405e-05	0.0041072	intron-variant	FANCD2	GRCh38.p7	3:10043169	AAGAGCTCATCCTCA[C/T]ACAGGATGTCACAAT	2177
rs763860470	snp	A/C			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082588	GAATTAATTTGAGCA[A/C]CCTATATAGCTTTTA	2177
rs763868772	snp	C/T	1.64806e-05	0.00287054	synonymous-codon	FANCD2	GRCh38.p7	3:10063818	GTTGCAGTTGGTTCA[C/T]TCCTGCAGTGAGCAG	2177
rs763897558	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10042328	AGGCTCTAAATGTAA[C/G]ATAATAGCTCTGTTT	2177
rs763986919	snp	G/T	1.65789e-05	0.0028791	missense	FANCD2	GRCh38.p7	3:10065942	AGCGTTCATTCATGT[G/T]TTCTCTCATATTTCT	2177
rs764042162	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10073738	ACATGGATCCCAATT[A/G]TTTCTGTTGATCAGC	2177
rs764049223	snp	G/T	0.00026347	0.0114746	intron-variant	FANCD2	GRCh38.p7	3:10065827	AGGTTTTATTGGCTT[G/T]CACTAAAGGTAGTTG	2177
rs764060161	snp	A/T	1.69951e-05	0.00291501	intron-variant	FANCD2	GRCh38.p7	3:10046543	ATGTACTGATTTGTT[A/T]ACTGTTTTTCTGTTG	2177
rs764060897	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10043316	TGTATGTGTTTATAT[A/G]TTTTCTTAGCCATTC	2177
rs764067352	in-del	-/AAT			intron-variant	FANCD2	GRCh38.p7	3:10053536	TATAATAATAATAAA[-/AAT]AATAAAATAAAATAG	2177
rs764098274	snp	A/C			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095556	ATGTTTACTTCTGCA[A/C]AGTCCTCTAGGTAAC	2177
rs764105093	snp	A/C	3.295e-05	0.00405881	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085878	TGTCCTTAGTAGCCG[A/C]CTGAAACAGGGAGAA	2177
rs764115368	snp	A/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082336	CCACTGCTTCCAGAC[A/T]CCCATTATCTCTCAA	2177
rs764145888	snp	A/G	1.67407e-05	0.00289311	intron-variant	FANCD2	GRCh38.p7	3:10039917	TGCAGTATGCAAAGA[A/G]CAGTAGTAATATGGT	2177
rs764195579	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086566	AGCTCACTGCACCCT[C/T]CACCTCCTGGGCTCA	2177
rs764205355	snp	A/G	1.64746e-05	0.00287002	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088509	ATAAAGAGAAGAGCA[A/G]CATCTCTAATGACCA	2177
rs764217987	snp	A/G	1.64822e-05	0.00287068	missense	FANCD2	GRCh38.p7	3:10052444	CGAAAACTCTTCTAT[A/G]TTCTCAGCACACTGG	2177
rs764221260	in-del	-/A	2.19807e-05	0.0033151	intron-variant	FANCD2	GRCh38.p7	3:10062261	CTTTTTTTTTTTTTT[-/A]AGAGAGTCTCGCTCT	2177
rs764234693	in-del	-/AC			intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10098990	TGGGACCCAGAAGAA[-/AC]AACGACACAATCTTA	2177
rs764244696	snp	C/G	3.29468e-05	0.00405861	missense	FANCD2	GRCh38.p7	3:10078141	CTGGAAGATCTCTCC[C/G]AGAAGCTGGAGAGTA	2177
rs764245894	in-del	-/CAAT			intron-variant	FANCD2	GRCh38.p7	3:10037258	GTTCAATTTTGTTAG[-/CAAT]CAAAGGCACAAATTT	2177
rs764285039	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10035598	CCTTTTCCTCCTCCT[C/T]GTCTCTTTTATTAAG	2177
rs764296912	snp	A/C	3.29549e-05	0.00405911	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088407	AGCAAGAATGAGGTC[A/C]AGTTCCCATATGTAA	2177
rs764386433	snp	C/G	1.64768e-05	0.00287021	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10081477	TTGGTAAGTATGTGG[C/G]AAGTGTGGAGAGAAC	2177
rs764391458	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10074732	AAGTTCCTCAGGTCT[A/G]TTCTTATTTCACAAA	2177
rs764399250	snp	A/G	3.29506e-05	0.00405884	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088786	CTGTAGTTGTATTCT[A/G]CTTTGTTAATTAGTG	2177
rs764430832	snp	G/T	1.64781e-05	0.00287033	intron-variant	FANCD2	GRCh38.p7	3:10042713	CAACTTAAGTGCCAA[G/T]TGCTCTTCTCTGTCC	2177
rs764445640	snp	A/C	1.67461e-05	0.00289357	intron-variant	FANCD2	GRCh38.p7	3:10072841	TGTGTAATTGGTACA[A/C]ATTGAGCTTCAGCCT	2177
rs764447374	snp	C/T	0.12568	0.216898	synonymous-codon	FANCD2	GRCh38.p7	3:10046720	ATTCTCTGTTCATTA[C/T]TTAGTAAGTGTCAGA	2177
rs764493820	snp	A/G	1.64735e-05	0.00286993	missense	FANCD2	GRCh38.p7	3:10042623	TACCTGTGATAATAA[A/G]GTTCATTCTTCATTC	2177
rs764507146	snp	A/G	3.62411e-05	0.00425667	missense	FANCD2	GRCh38.p7	3:10034797	CAGGATGAGGAAGCC[A/G]GGTGTGGAGAGGAGG	2177
rs764524624	snp	C/T			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027641	CGGGCGCGGTTGGCT[C/T]ACGCCTGTAATCCCA	2177
rs764559682	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10066592	GAAATACTTAGAAAG[A/G]TTAAAGACTCAGCCA	2177
rs764562105	in-del	-/C			intron-variant	FANCD2	GRCh38.p7	3:10030725	GCCAACATAGTGAAA[-/C]CCCATCTCTACTAAA	2177
rs764640522	snp	A/G	3.32851e-05	0.00407939	intron-variant	FANCD2	GRCh38.p7	3:10062117	TAAAACTTAAAGTAT[A/G]ATAATAATTTAAAAA	2177
rs764649105	in-del	-/T	1.64811e-05	0.00287059	frameshift-variant, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101255	GAGTTATGATGACTC[-/T]TGATTAGACCCCAGA	2177
rs764665698	snp	A/G	1.65053e-05	0.0028727	intron-variant	FANCD2	GRCh38.p7	3:10028740	AGTATCTAGTCATTT[A/G]TTGCTTTATTTCCTG	2177
rs764667302	snp	C/T	3.72176e-05	0.00431363	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095312	TCAGCAGCCTGCCTG[C/T]TGGCTTAATCTGCAG	2177
rs764679262	snp	A/G			intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10099413	GGATTGCTTGAGTCC[A/G]GGAGCTCAAGGCAAA	2177
rs764688577	in-del	-/AGA			intron-variant	FANCD2	GRCh38.p7	3:10051901	TCCTTCCAGATCTGT[-/AGA]GAAAGGAGAAATAAT	2177
rs764697233	snp	A/C	6.6291e-05	0.00575683	intron-variant	FANCD2	GRCh38.p7	3:10047870	TTAGGTTGTGTACTA[A/C]CTGTTTCCTACAGCT	2177
rs764709877	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10060900	CATTACAAACCGACA[C/T]TGGATTTCAGTTCAT	2177
rs764761668	in-del	-/T			intron-variant	FANCD2	GRCh38.p7	3:10062248	TTTCTTTTTCCTGTC[-/T]TTTTTTTTTTTTTAG	2177
rs764769075	snp	A/C			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098580	CTCTAGATGCTGAAT[A/C]ACAAGTTGGTATCCA	2177
rs764775864	snp	C/T	6.67991e-05	0.00577885	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090342	CTGAACTAGAGAAGA[C/T]GGTGAAAAAAATTGA	2177
rs764801338	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10051998	AGAATATTGTTTTCA[C/G]TGAAAAAAAAGGGAA	2177
rs764807366	snp	C/T	5.02273e-05	0.0050111	intron-variant	FANCD2	GRCh38.p7	3:10043469	AGTAATTTTTTTCCT[C/T]TCTGCTACTTGTAGT	2177
rs764807429	snp	A/G	4.94173e-05	0.00497053	missense	FANCD2	GRCh38.p7	3:10049428	AATGAAGCTGAAGTT[A/G]ATACTGCCTTAGATG	2177
rs764813313	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10030014	GCTGTCTGGAACTCC[C/T]GACCTCAAGTGATCC	2177
rs764832852	snp	C/G	0.000116166	0.00762034	missense	FANCD2	GRCh38.p7	3:10060401	CATCATGGCGGCAGA[C/G]AGGTACACGTGGAGA	2177
rs764851623	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10067612	AGACCAGCCTGGCCA[A/T]CATGGTGAAACCCTG	2177
rs764864045	snp	A/T			intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10099611	GAAAATACAAAAATT[A/T]GCTGGGTGTGGTGGC	2177
rs764865805	snp	C/T	1.64749e-05	0.00287005	intron-variant, missense	FANCD2, FANCD2OS	GRCh38.p7	3:10098936	CTTCTATGCCCATTT[C/T]CATTCCCTCCATAAC	2177
rs764866110	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085424	TTGAGATGGAGTCTC[A/G]CTCTGTCGCCAGGCT	2177
rs764876175	snp	C/G	1.65581e-05	0.00287728	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085971	CCAAGAAACTCCTAG[C/G]AACAGGATTGGCAAC	2177
rs764893663	snp	A/C	1.65438e-05	0.00287605	missense	FANCD2	GRCh38.p7	3:10043554	GTAATAAAGTCAGCT[A/C]TTAGATATGAGAAAA	2177
rs764903036	snp	C/T	6.5999e-05	0.00574414	missense	FANCD2	GRCh38.p7	3:10074555	GGAAGGAAGAAAAGA[C/T]ATCATTGTTACTACA	2177
rs764910988	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10050644	AAAAAAAAAAAAAAA[G/T]GCTTAGAAGAGCACA	2177
rs764943441	snp	A/G			missense	FANCD2	GRCh38.p7	3:10052408	TTAGATTATCTGGAT[A/G]ACATATCCCCTCAGC	2177
rs764953775	snp	G/T	3.30071e-05	0.00406232	intron-variant	FANCD2	GRCh38.p7	3:10073390	TGGGTATCCGTGAAG[G/T]TTTGTGACATCCCAG	2177
rs764962539	snp	A/G	1.67438e-05	0.00289338	missense	FANCD2	GRCh38.p7	3:10039301	AGTGATGAAATCAAC[A/G]TACCTCGACTCATTG	2177
rs764970342	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10058202	TGGAGATTAGGCCCA[C/T]TCTTGTGCTTGTCTC	2177
rs764986328	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10056729	TCATTCTGATGAGTG[C/T]GAGTGGTATCTCATT	2177
rs765036045	snp	A/T	9.25969e-05	0.00680367	intron-variant	FANCD2	GRCh38.p7	3:10066028	TGCATAGTTTTTCTC[A/T]AAACTATTTTCTTAG	2177
rs765036767	in-del	-/G	1.67427e-05	0.00289328	intron-variant	FANCD2	GRCh38.p7	3:10049554	AATACTATAATTGGT[-/G]GGAGGTGGTGGGAAG	2177
rs765039708	snp	C/T	1.64741e-05	0.00286998	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094241	TGCCTCAGGGGCCTT[C/T]CAGTGAGATACCTCA	2177
rs765059939	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10074458	TGCATATTTGTACTT[C/T]GAAGTTTTTATTAAA	2177
rs765076566	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10077800	ATTGGGAGGCCAAGG[C/G]AGAAGGATCATCTGA	2177
rs765082165	snp	A/C	3.29843e-05	0.00406092	missense	FANCD2	GRCh38.p7	3:10034493	AAATAGCTTTCCAAA[A/C]GAAGCTCTTTCAGAC	2177
rs765109583	snp	A/G			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027162	AGAAATTTTCCTTAT[A/G]CCGGTAACTATGCTG	2177
rs765128164	snp	C/T	6.59261e-05	0.00574097	missense	FANCD2	GRCh38.p7	3:10063885	GCCAACCTGATCCAA[C/T]ATGAAAAGCTGGATC	2177
rs765139793	in-del	-/T			intron-variant	FANCD2	GRCh38.p7	3:10058922	AATCACTTTGAATGG[-/T]TATTAGCAATATTAA	2177
rs765154899	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10030751	CTAAAAATACAAAAA[G/T]TAGCTGGGCGTGGTG	2177
rs765204178	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10080063	GGGACTACAGGTGCA[C/T]GCCACCACACCCAGC	2177
rs765205079	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10059554	ACCCCTGTAATCCCA[G/T]CACTTTGGGAGGCCA	2177
rs765208098	snp	A/G	1.64738e-05	0.00286995	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087177	CATCAAAGCATTCCC[A/G]GTTTCCAGTGTGCTC	2177
rs765247439	snp	G/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094437	CCTTGGTGACTCCTG[G/T]GTGGGGCTGGGAGTG	2177
rs765268017	snp	G/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093581	GGCAGTTGAGTTTAG[G/T]AGCAGTAGTTACCTT	2177
rs765278239	snp	A/C	3.3413e-05	0.00408722	intron-variant	FANCD2	GRCh38.p7	3:10032997	TAATCTAATTTTATT[A/C]TCTGGGTTTAATGAA	2177
rs765310114	in-del	-/G			intron-variant	FANCD2	GRCh38.p7	3:10037010	CCAGCTAATTTTCGT[-/G]GTTTTTTTTTTTTTG	2177
rs765312571	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098503	TAAGATGAACCTTTC[A/G]TTACATTACTTATTG	2177
rs765324038	snp	A/G	1.64846e-05	0.0028709	missense	FANCD2	GRCh38.p7	3:10052459	GTTCTCAGCACACTG[A/G]CATTTAGCAAACAGA	2177
rs765339192	snp	C/T	3.29511e-05	0.00405887	missense	FANCD2	GRCh38.p7	3:10046623	TCTATAGCACCAATA[C/T]TCAGACAAAGAAGTA	2177
rs765365413	snp	G/T	3.33856e-05	0.00408555	missense	FANCD2	GRCh38.p7	3:10065955	GTGTTCTCTCATATT[G/T]CTTACTCTCAACTGG	2177
rs765378218	snp	C/G	0.000166575	0.00912468	missense	FANCD2	GRCh38.p7	3:10046710	TCCAGAGTACATTCT[C/G]TGTTCATTACTTAGT	2177
rs765382538	snp	C/T	1.6857e-05	0.00290314	intron-variant	FANCD2	GRCh38.p7	3:10039924	TGCAAAGAGCAGTAG[C/T]AATATGGTCTCTTCT	2177
rs765471096	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10058017	CTATCAAGTTTGCCC[C/T]TTCTGCCTTCTTAAT	2177
rs765475036	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084546	CTCAAGTGATCCACC[C/T]GCCTCAGCCTCCCAA	2177
rs765475407	snp	C/T	1.80641e-05	0.00300528	intron-variant	FANCD2	GRCh38.p7	3:10052547	TTTTGAGACAGAGTC[C/T]AGCTCTGTCTCCTAG	2177
rs765498613	in-del	-/T	1.65083e-05	0.00287296	intron-variant	FANCD2	GRCh38.p7	3:10073400	TGAAGGTTTGTGACA[-/T]CCCAGTGAGATTAAC	2177
rs765504399	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085097	AGGGGTAAGTACCAC[C/T]ATGGGCTGGACATTG	2177
rs765542844	snp	G/T			upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026286	TCTGGGCCTTCTCTC[G/T]CCCCTATGCCCGGCT	2177
rs765550790	snp	A/T	1.64857e-05	0.00287099	missense, downstream-variant-500B	FANCD2, FANCD2OS	GRCh38.p7	3:10081131	ATATTGGATTCTCAC[A/T]TCTCCAACAGAGATC	2177
rs765576835	snp	C/T	3.29685e-05	0.00405995	missense	FANCD2	GRCh38.p7	3:10036306	CCATTATCAAAACCT[C/T]ATTTGAGAAGTTGCC	2177
rs765595855	snp	A/G			upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025047	CAGCCTCGAACTCCC[A/G]GGCTCAAGTGATCCT	2177
rs765602981	snp	G/T	4.94287e-05	0.00497111	intron-variant	FANCD2	GRCh38.p7	3:10035267	CTGTGAACATTTGAT[G/T]GAAGAGGTTTGTGGT	2177
rs765642591	snp	C/T	1.87665e-05	0.00306315	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098684	CCTAAATGTGATCAT[C/T]ATAACCCACCATTTT	2177
rs765666007	snp	A/C/G	4.98131e-05	0.00499044	missense	FANCD2	GRCh38.p7	3:10043146	AAAAGTAAAGGACGA[A/C/G]CAAGGTAAAGAGCTC	2177
rs765672800	snp	A/G	3.29473e-05	0.00405864	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085862	TGTATTCAGCCCTCC[A/G]TGTCCTTAGTAGCCG	2177
rs765677370	snp	G/T			missense	FANCD2	GRCh38.p7	3:10078125	TGAGCTGCTTTTCTT[G/T]CTGGAAGATCTCTCC	2177
rs765694013	snp	A/G	1.65781e-05	0.00287902	intron-variant	FANCD2	GRCh38.p7	3:10072864	TTCAGCCTGCTGTTT[A/G]TTTCAGTCACCCCAG	2177
rs765697450	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10072260	TCTCATGTGCGCCAT[A/G]AATATATATATACCT	2177
rs765738706	snp	C/T	3.29468e-05	0.00405861	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092159	TGTGACTCAGAGGTG[C/T]CCATATATTTGGCTG	2177
rs765767053	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093468	GGGAAGGCAATGGAT[A/G]CATTTTCCCACCCTA	2177
rs765774544	snp	A/C	1.64741e-05	0.00286998	missense	FANCD2	GRCh38.p7	3:10047959	CTGTCGCTGGCTCAG[A/C]GTTTGCTTCACTCTC	2177
rs765783995	snp	A/C/G	3.29458e-05	0.00405857	missense	FANCD2	GRCh38.p7	3:10064425	TCCTGTGTTGTTCCG[A/C/G]AAGGGTAGGTATTGT	2177
rs765784176	snp	C/G	2.22497e-05	0.00333532	intron-variant	FANCD2	GRCh38.p7	3:10073023	TGTGTCTCTAAATAA[C/G]CTTCATTGAATTAAC	2177
rs765793991	snp	C/T	5.56344e-05	0.00527391	intron-variant	FANCD2	GRCh38.p7	3:10062243	CTTTCTTTCTTTTTC[C/T]TGTCTTTTTTTTTTT	2177
rs765799837	snp	A/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097996	TTATAAGGTTTTTTT[A/T]AGTTGTCTGATTAGC	2177
rs765828012	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10063298	AAAAATTAGCTGGAC[A/T]TGGTGGCAGGCGCCT	2177
rs765840374	snp	C/G/T	3.29491e-05	0.00405877	missense, stop-gained, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096387	AGACCCTGGAACTTT[C/G/T]AGTTTGCAGAGTCAA	2177
rs765845616	snp	A/G	1.65787e-05	0.00287907	intron-variant	FANCD2	GRCh38.p7	3:10028767	CCTGTAGCAATGTGT[A/G]AGGCATGTGAGAGAT	2177
rs765865952	snp	A/T	1.68681e-05	0.00290409	intron-variant	FANCD2	GRCh38.p7	3:10043018	CCACTATGAATGAGC[A/T]GAAAACCATAGCTAA	2177
rs765871035	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10078314	TCACTGGGTAGCATG[C/G]GTGCAGCCGTATTGC	2177
rs765934352	snp	G/T	1.64798e-05	0.00287047	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10081496	TGTGGAGAGAACTGA[G/T]TATATACTTGCTTTT	2177
rs765952227	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10066672	CTGTCTGGCTATTCC[A/G]CCTTGTAACATAACT	2177
rs765976136	snp	C/G	1.64879e-05	0.00287118	intron-variant	FANCD2	GRCh38.p7	3:10047892	CCTACAGCTTCTTTT[C/G]TCTCTCTACTCTTCC	2177
rs766008512	snp	C/T	1.64727e-05	0.00286986	synonymous-codon	FANCD2	GRCh38.p7	3:10065413	GTGTCTCCGCTGTGC[C/T]TGGCTCCGTATTTCC	2177
rs766042324	snp	A/G	1.64743e-05	0.00287	missense	FANCD2	GRCh38.p7	3:10039776	CAGAGAACCTGCAGC[A/G]TGACATCATCACCAG	2177
rs766049281	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10075160	GTGGAAATAGCTAGC[A/G]ATACGGTAGCTTTAT	2177
rs766065907	snp	A/T	1.65504e-05	0.00287662	missense	FANCD2	GRCh38.p7	3:10043568	TATTAGATATGAGAA[A/T]ACCATTTCAGAAGCC	2177
rs766098612	snp	A/G	0.000148816	0.00862471	missense	FANCD2	GRCh38.p7	3:10032939	AAGATATCAGGAATT[A/G]TTCTTAAAACGGGAG	2177
rs766103472	snp	G/T	1.78592e-05	0.00298819	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087296	CTTTTTTTTTTTTTT[G/T]TTTTAATGAATAGGA	2177
rs766118736	snp	C/G	1.6593e-05	0.00288031	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095244	CCAGTTGGACACAAG[C/G]CTGCTTCATCACCTG	2177
rs766168539	snp	C/T	1.64808e-05	0.00287057	missense	FANCD2	GRCh38.p7	3:10074665	TTAGATACTGAAATG[C/T]ACACTGAAGTAAGTG	2177
rs766172452	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10042154	ACCCCCCTCGGCCTC[C/T]CAAAGTGCTGGGATT	2177
rs766192092	snp	C/T	1.64743e-05	0.00287	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087203	TGCTCTTTATCTCAT[C/T]AGACTTTTGATGGTT	2177
rs766199957	snp	A/C			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084883	GAAAGCAGTGGTTTA[A/C]GAAAACACTTCTGGC	2177
rs766241610	snp	C/T	1.67153e-05	0.00289091	missense	FANCD2	GRCh38.p7	3:10034707	AAGATAATAGAAGAA[C/T]TTGTTAGTGGCCTGG	2177
rs766259987	snp	C/T	1.64993e-05	0.00287218	synonymous-codon	FANCD2	GRCh38.p7	3:10049455	GATGTCCTTCTAGAG[C/T]TGGTAGTGTTAAACC	2177
rs766286504	snp	A/G	8.24463e-05	0.00642	synonymous-codon	FANCD2	GRCh38.p7	3:10074565	AAAGACATCATTGTT[A/G]CTACATAATTCCCAT	2177
rs766340368	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10058035	CTGCCTTCTTAATTC[C/T]GGCAAAGATCATTTT	2177
rs766357171	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10077470	TGAGGCAGGAGAATT[A/G]CTTGAACCTGGGACG	2177
rs766364633	snp	C/T	1.65787e-05	0.00287907	intron-variant	FANCD2	GRCh38.p7	3:10064311	TCTAGGGCTGTACAG[C/T]AAGTACACTCTGCAC	2177
rs766391203	snp	A/C	6.5962e-05	0.00574253	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10098969	CTTCTGTGCTTATAT[A/C]ATTTTTGGGACCCAG	2177
rs766411763	in-del	-/CCA	1.64868e-05	0.00287109	cds-indel	FANCD2	GRCh38.p7	3:10052488	GAATGAAGCCAGCAG[-/CCA]CATCCAGGTAAGAGG	2177
rs766425393	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10080933	AGTCATTGGAAGATG[A/G]AGCAAGATTTTTATC	2177
rs766436266	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10047560	ATAGACCTACTTCAA[A/G]TTATAACCAAGGTGG	2177
rs766503562	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10046148	AAGCTCTGCCTCCCG[A/G]GTTCACGCCATTCTC	2177
rs766529679	snp	A/G	4.94637e-05	0.00497287	missense	FANCD2	GRCh38.p7	3:10060354	TTCAAGTACAAGCTC[A/G]TTGGGATTATTGGTG	2177
rs766532127	snp	A/G	3.29511e-05	0.00405887	missense	FANCD2	GRCh38.p7	3:10041685	TCCTTTCAAGCCTCC[A/G]ACTTGACCCAAACTT	2177
rs766539616	in-del	-/AATA			intron-variant	FANCD2	GRCh38.p7	3:10055834	AAATAATAATAAATA[-/AATA]AATAAATAAATAATT	2177
rs766567785	snp	A/G	0.000290884	0.0120564	missense	FANCD2	GRCh38.p7	3:10067267	GGAAGGTGCTCACTC[A/G]GTTAAAGCACATTGT	2177
rs766587099	in-del	-/CAG	1.7894e-05	0.0029911	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087284	GGGCCTAGATCCTTT[-/CAG]TTTTTTTTTTTTTTT	2177
rs766592848	snp	C/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097222	GAAATTGCTAATGAA[C/G]TTTTGGGCACCACTG	2177
rs766605179	in-del	-/TGAGAG	0.000230814	0.0107403	cds-indel, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098764	GGAGAGCACAGCAGA[-/TGAGAG]TGAGGATGACATGTC	2177
rs766619451	snp	C/T	8.25157e-05	0.0064227	synonymous-codon	FANCD2	GRCh38.p7	3:10046696	TCAAGAACAGCTGCT[C/T]CAGAGTACATTCTCT	2177
rs766662733	snp	C/T	1.64803e-05	0.00287052	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098793	ACATGTCATCCCAGG[C/T]CTCCAAGAGCAAAGC	2177
rs766698512	snp	C/T	1.64741e-05	0.00286998	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088825	ATTTGACTCTCAATG[C/T]AGTATCTACCTGGAG	2177
rs766703375	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10068944	TGGATATCCATATGC[A/G]GAAGAATGAAACTAG	2177
rs766723020	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088224	TGTTTCAAGATGGGG[C/T]TGGGGTGGGACGTGT	2177
rs766737260	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10040028	TGAATAGATCCACAT[A/G]CTTTCTTTTTTTTTT	2177
rs766748440	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10055022	TGTTCTGAGAATTTA[C/T]AAATTTGTGTTTACC	2177
rs766748480	snp	C/T	1.83778e-05	0.00303126	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098691	GTGATCATTATAACC[C/T]ACCATTTTCTTGGTC	2177
rs766750638	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10037184	AATAGAAAAGTAGAC[A/T]AAGGTCATGAACAGA	2177
rs766779543	snp	C/T	1.64762e-05	0.00287016	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088995	CTTAAGATAGAATCA[C/T]CATCAGGCTGGGCAC	2177
rs766781553	snp	C/T			upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10024696	AAAATTAAAAATTTC[C/T]TGCGGAATTTGCAAA	2177
rs766821340	snp	C/T			missense	FANCD2	GRCh38.p7	3:10042587	TGATGGATAAGTTGT[C/T]GTCTATTAGATTGGA	2177
rs766822617	snp	A/G	7.14235e-05	0.0059755	intron-variant	FANCD2	GRCh38.p7	3:10039249	GACCAGAAAGGCTCA[A/G]TTCCCTGTTTTCTCT	2177
rs766865689	snp	A/G	1.64942e-05	0.00287173	missense	FANCD2	GRCh38.p7	3:10073352	CATCTCATAGAGGCC[A/G]GCTAAACAAGGTATT	2177
rs766876118	in-del	-/T/TT	0.355897	0.243807	intron-variant	FANCD2	GRCh38.p7	3:10035158	TGGAAAACAGATTTC[-/T/TT]TTTTTTTTTTACAGT	2177
rs766921614	snp	C/T	1.64746e-05	0.00287002	missense	FANCD2	GRCh38.p7	3:10048020	TCCTATACAAATATG[C/T]ATTTAAGTTTTTTGA	2177
rs766926932	snp	A/G	1.66161e-05	0.00288232	synonymous-codon	FANCD2	GRCh38.p7	3:10043148	AAGTAAAGGACGAGC[A/G]AGGTAAAGAGCTCAT	2177
rs767002477	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10075892	CCTGCCACCATGCCT[C/G]GCTAATTTTTTGTAT	2177
rs767016530	snp	A/G	1.64923e-05	0.00287156	synonymous-codon	FANCD2	GRCh38.p7	3:10036325	TGAGAAGTTGCCAGA[A/G]TATTTTTTTGAAAAG	2177
rs767066676	snp	A/G			intron-variant, utr-variant-5-prime, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026508	GTCGTAGTCTCTCGA[A/G]GCCCCGCTCCCCTGC	2177
rs767075732	snp	A/G	1.64749e-05	0.00287005	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085873	CTCCATGTCCTTAGT[A/G]GCCGACTGAAACAGG	2177
rs767089204	in-del	-/TCA	1.6476e-05	0.00287014	intron-variant	FANCD2	GRCh38.p7	3:10035243	CTGCAGGTAAGACTG[-/TCA]CTTTTTCTGTGAACA	2177
rs767109599	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10050955	CCTGGGCATTGTGGT[A/G]CATGCCTGTAATCCC	2177
rs767119830	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10039863	GGATAAACCCTCTGT[C/T]ATCATCTAAGTGAGG	2177
rs767122938	snp	A/T	9.95405e-05	0.0070541	intron-variant	FANCD2	GRCh38.p7	3:10043041	ATAGCTAATATTTAC[A/T]TTCTGCAGGTAATTT	2177
rs767147846	snp	A/C/T	8.79169e-05	0.00662953	intron-variant	FANCD2	GRCh38.p7	3:10062261	TCTTTTTTTTTTTTT[A/C/T]AGAGAGTCTCGCTCT	2177
rs767157859	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10056777	TTCTAATGACTAATG[A/T]TGTTAAGCATCTTTT	2177
rs767163581	snp	A/G	1.65048e-05	0.00287265	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092268	GTGAGTATGGAGACT[A/G]CTTGACACATCTCAC	2177
rs767175010	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098637	ATATCTTCCTTTGTA[C/T]TGCCTGTAAACTCAA	2177
rs767176870	snp	A/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082431	ATCTTCCTAACATAA[A/T]CCCAGTTTGATCCTA	2177
rs767200718	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10074362	ATCTTAAATTAGGTG[C/G]TCTGTCTTGGGAATA	2177
rs767238170	snp	C/T	1.64738e-05	0.00286995	missense	FANCD2	GRCh38.p7	3:10047975	GTTTGCTTCACTCTC[C/T]AGACCAGAGTATAAT	2177
rs767264056	in-del	-/TAC			intron-variant	FANCD2	GRCh38.p7	3:10074917	TCCTTACATTTAGGT[-/TAC]TACTACTACTACTAC	2177
rs767270364	snp	A/G	1.64972e-05	0.00287199	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085946	TAACTACATAGCCAA[A/G]ATTGTTGTCCCAAGA	2177
rs767287258	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10059835	AAAGTCCCCATTTCA[C/T]AGATGTAAAAATTAA	2177
rs767300525	snp	C/T	1.64893e-05	0.0028713	intron-variant	FANCD2	GRCh38.p7	3:10065522	GTCATCAGATCCTTT[C/T]TTCTTTATACTCTTC	2177
rs767356553	in-del	-/AT			intron-variant	FANCD2	GRCh38.p7	3:10054436	TATACATGTATATAC[-/AT]ATGTATATACATATA	2177
rs767369907	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10031989	TAGTTGGTATTACAG[G/T]CGCACGCCACCACAC	2177
rs767383807	snp	A/G	3.34018e-05	0.00408654	synonymous-codon	FANCD2	GRCh38.p7	3:10043831	CCTGTTTTTTCAGGC[A/G]ATTGAAAACACTGCC	2177
rs767415779	snp	G/T	4.99604e-05	0.00499777	intron-variant	FANCD2	GRCh38.p7	3:10039906	GGTTCTATCACTGCA[G/T]TATGCAAAGAGCAGT	2177
rs767416501	snp	A/G	1.64849e-05	0.00287092	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101195	CCCCTTAGGATGGTG[A/G]AGAAGACGAAGTAAG	2177
rs767496500	snp	C/G/T	8.23695e-05	0.00641707	synonymous-codon	FANCD2	GRCh38.p7	3:10078107	TGTGCAACTTGGGCC[C/G/T]CCTGAGCTGCTTTTC	2177
rs767512318	snp	C/T	3.29679e-05	0.00405991	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094393	CAGAGAACAAAGATA[C/T]GCACTGAAGAGTTGC	2177
rs767539823	snp	A/C/T	3.29469e-05	0.00405864	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092165	TCAGAGGTGCCCATA[A/C/T]ATTTGGCTGCCCCAG	2177
rs767563088	snp	C/G	1.70261e-05	0.00291766	splice-donor-variant, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095275	TGTGGGCATTCCAAG[C/G]TAAGAAGGGGAGCAG	2177
rs767565704	snp	A/T	1.95888e-05	0.00312954	intron-variant	FANCD2	GRCh38.p7	3:10046769	TAAAACAGAAAGCTT[A/T]ACAGCTCTCATGTAA	2177
rs767572680	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10072561	TTGGGGTTACAGGCG[C/T]GAGCCACCCTGCCTG	2177
rs767590233	snp	C/T	3.47735e-05	0.0041696	missense	FANCD2	GRCh38.p7	3:10067282	GGTTAAAGCACATTG[C/T]AGAATTGCAAATAAT	2177
rs767621552	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10069117	GGAATACCCTACAAG[C/G]ACAGGCAACCAAAGC	2177
rs767632795	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10062927	GCTGGTCTCAAACTC[C/G]TGATCTCAGGTGATC	2177
rs767659342	snp	C/T	8.24667e-05	0.00642079	missense	FANCD2	GRCh38.p7	3:10034519	CAGACCCTGAGGAGA[C/T]ACCCTTCCTATCCCA	2177
rs767699213	snp	A/G	1.66228e-05	0.0028829	missense	FANCD2	GRCh38.p7	3:10049476	GTGTTAAACCCATCT[A/G]CTATGATGATGAATG	2177
rs767726902	in-del	-/TTAT	4.98956e-05	0.00499453	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101162	AGTAACCTAAAATGC[-/TTAT]TTATTTATTCTTTGC	2177
rs767752184	snp	A/C	1.64735e-05	0.00286993	missense	FANCD2	GRCh38.p7	3:10042609	TAGATTGGAGGATTT[A/C]CCTGTGATAATAAAG	2177
rs767793794	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10080544	GGGAGTCCAAGATGG[A/G]TGGATTGCTTGAGCT	2177
rs767806932	snp	C/T	3.31978e-05	0.00407404	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090318	TTGTTTTCTTCCGTG[C/T]GATGATGGCTGAACT	2177
rs767829874	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10061541	CCTTTGTAGACTCAC[A/G]TCAGCAATAAGGATA	2177
rs767841886	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10039208	GCTAAAATATTTTGT[A/G]CAGTATTAATGCTTG	2177
rs767852537	snp	C/T	1.65902e-05	0.00288008	missense	FANCD2	GRCh38.p7	3:10046707	TGCTCCAGAGTACAT[C/T]CTCTGTTCATTACTT	2177
rs767860064	snp	A/T	3.29598e-05	0.00405941	missense, downstream-variant-500B	FANCD2, FANCD2OS	GRCh38.p7	3:10081170	AAATTGTTCATTGTG[A/T]TTTTCAACTGCTGAC	2177
rs767862240	snp	G/T	1.71299e-05	0.00292654	intron-variant	FANCD2	GRCh38.p7	3:10060273	CCAGCATTTTCATCT[G/T]TCTTCATCATCTCAT	2177
rs767888603	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10063460	AAAAGAAAAAGCTAT[C/T]TGAGAGAGAAAACAG	2177
rs767893462	snp	C/T	0.000115313	0.0075923	intron-variant, missense	FANCD2, FANCD2OS	GRCh38.p7	3:10098922	TTTATTGTCAAATGC[C/T]TCTATGCCCATTTCC	2177
rs767896927	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10074786	AAGTTAGACTGACTT[C/T]TAAAGCCTTTATATG	2177
rs767897539	snp	G/T	1.64825e-05	0.00287071	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10089002	TAGAATCATCATCAG[G/T]CTGGGCACGGTGGCA	2177
rs767897981	snp	G/T	1.65523e-05	0.00287678	intron-variant	FANCD2	GRCh38.p7	3:10064322	ACAGCAAGTACACTC[G/T]GCACTGCCCTTTTTG	2177
rs767899076	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10036892	CCAGGCTGGAGTGCC[A/G]TAGTACGATCATGGC	2177
rs767901156	snp	A/T	4.9423e-05	0.00497082	missense, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10081346	CATTTTTATTTTTAG[A/T]GTTTAGCTGCTGAGA	2177
rs767929606	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10066285	TATGCCTACTGTTTT[A/G]ATTCAGTGAGTGGTG	2177
rs767995408	snp	A/G	1.64741e-05	0.00286998	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087163	ACTTGCAGAATTTCC[A/G]TCAAAGCATTCCCAG	2177
rs768012206	in-del	-/T			upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025774	ACAGCACCGTTTTTG[-/T]TTTTTTGTTTTTAAC	2177
rs768055050	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10051889	TTTCCTTGTGACTCC[A/T]TCCAGATCTGTAGAG	2177
rs768078549	snp	C/G	1.64817e-05	0.00287064	intron-variant	FANCD2	GRCh38.p7	3:10039672	ACGTAGGTAGTCTTT[C/G]TTTATTCTGGGTAAT	2177
rs768078884	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10055054	GTAGTTTCCTTTCCC[C/T]TCTTGTTCTACATCA	2177
rs768087156	snp	C/T	1.64765e-05	0.00287019	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094361	AGTTTTAGAAAACAC[C/T]GGGTAAGAGCTAAGA	2177
rs768088140	snp	A/C	1.65638e-05	0.00287778	intron-variant	FANCD2	GRCh38.p7	3:10064879	ATCAGGCCAAAAGTC[A/C]GTATAGTTTTTCTTT	2177
rs768088809	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10037427	GTTCAGGCATCGATT[C/T]GGAAGAGCAATAGAT	2177
rs768105189	snp	C/T	4.95005e-05	0.00497471	missense	FANCD2	GRCh38.p7	3:10060382	GTGCTGTGACCATGG[C/T]TGGCATCATGGCGGC	2177
rs768118340	in-del	-/CTTT	0.000101894	0.00713697	intron-variant	FANCD2	GRCh38.p7	3:10062228	TGAGTTCTTTTTTTC[-/CTTT]CTTTCTTTTTCCTGT	2177
rs768134945	snp	A/G	1.64727e-05	0.00286986	synonymous-codon	FANCD2	GRCh38.p7	3:10049412	CCATATCTGCAGTGG[A/G]AATGAAGCTGAAGTT	2177
rs768145180	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10036493	TGGAGTGTCTTTGAA[A/G]TTTCATCTATTAATA	2177
rs768164124	snp	A/G	7.32011e-05	0.0060494	intron-variant	FANCD2	GRCh38.p7	3:10034659	AAATATTAAACTAAA[A/G]ATTTTATTCTTTTTT	2177
rs768250261	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098096	TTTTCTTTCATGCTT[A/G]CAATATCTGAGTCTT	2177
rs768282950	snp	C/T	1.65444e-05	0.00287609	synonymous-codon	FANCD2	GRCh38.p7	3:10043535	TATTATTCTCCTCTT[C/T]GATGTAATAAAGTCA	2177
rs768315440	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10048874	CTATTATGGAGTGAC[A/G]GTATAAAGGGAGAAT	2177
rs768330947	snp	C/T	3.30071e-05	0.00406232	intron-variant	FANCD2	GRCh38.p7	3:10063941	CTTTTCTTAAAGCAA[C/T]AAAGCATGAGAGCTG	2177
rs768355956	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10076788	TGGAGTGCAGTGGCA[C/T]GATCTTGGCTTACTG	2177
rs768414107	snp	C/T	5.35165e-05	0.00517256	intron-variant	FANCD2	GRCh38.p7	3:10052540	TTTTTTTTTTTGAGA[C/T]AGAGTCTAGCTCTGT	2177
rs768444104	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10074241	GAACCACCACACCTG[A/G]CCAGCTCACAGTTTT	2177
rs768450402	snp	A/G	1.6495e-05	0.0028718	missense, downstream-variant-500B	FANCD2, FANCD2OS	GRCh38.p7	3:10081118	AAAGGAAGCCGGAAT[A/G]TTGGATTCTCACATC	2177
rs768467457	snp	A/C			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096799	TAGATTCATAATAAC[A/C]TTTTTGTATAGGGAC	2177
rs768473175	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084110	GCGATTCTTCTGCCT[C/T]AGCCTCCTGAATAGC	2177
rs768483495	snp	C/T	3.30011e-05	0.00406195	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081251	GCCTAGACTTAGAAG[C/T]TGCTAAGCAAATATG	2177
rs768507092	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10077578	AATTTTTTTTTCACC[C/T]ATTGGGAAGTATTAA	2177
rs768543551	snp	C/G	4.94368e-05	0.00497152	synonymous-codon	FANCD2	GRCh38.p7	3:10046675	TAAGATTCGATCAGG[C/G]TGCATTCAAGAACAG	2177
rs768544539	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10076766	AGTCTTGCTCTGTCC[A/G]TCAGTCTGGAGTGCA	2177
rs768572935	snp	A/G	1.64904e-05	0.00287139	missense	FANCD2	GRCh38.p7	3:10064845	TTGCAAAAGATGGGG[A/G]TCCGGTGACCTCACA	2177
rs768603657	in-del	-/TTATTGG	1.69172e-05	0.00290832	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095187	AGAGCATTTATAAAC[-/TTATTGG]TTATAGGAAGATGTT	2177
rs768608195	snp	A/G	0.000263587	0.0114771	synonymous-codon	FANCD2	GRCh38.p7	3:10064756	TCCTGTGAAAGCACT[A/G]TACGGACTGGAAGAA	2177
rs768609277	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10059532	ATTTCGGGCCAGGCA[A/C]GTAATCACCCCTGTA	2177
rs768627472	snp	C/T	8.24151e-05	0.00641878	intron-variant	FANCD2	GRCh38.p7	3:10042508	CAGTTCAGTACAAAG[C/T]TGAGGTAGTGACATG	2177
rs768718346	in-del	-/T	4.94364e-05	0.0049715	intron-variant	FANCD2	GRCh38.p7	3:10042532	TGACATGAAAACCTA[-/T]TAAGTTTCTGTGCTT	2177
rs768738379	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10068106	TTATATAATACCACT[A/T]TTATAAAATACAGTA	2177
rs768739157	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10037851	TTGCAATAAGTAGTT[C/G]AGTATTTTGTTTAAA	2177
rs768772953	snp	C/T	1.67049e-05	0.00289002	intron-variant	FANCD2	GRCh38.p7	3:10036382	AAGTACCCTGATGTA[C/T]TTAAGTTCTCTCTGA	2177
rs768774007	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10048086	TTGGCAAGGAGGGAA[A/C]ACAGAAAGGGAAAAT	2177
rs768775835	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087954	GCCCAGCCCTGGCCT[C/T]TTTCTTAAACTGTCT	2177
rs768793095	snp	A/C	1.88973e-05	0.00307381	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098681	TACCCTAAATGTGAT[A/C]ATTATAACCCACCAT	2177
rs768816064	snp	A/C	1.9098e-05	0.00309009	intron-variant	FANCD2	GRCh38.p7	3:10072993	ATAGGTAAGTATGTT[A/C]TTTTCCTCTTGTCTT	2177
rs768821254	in-del	-/TC	5.16569e-05	0.00508191	intron-variant	FANCD2	GRCh38.p7	3:10034667	AACTAAAAATTTTAT[-/TC]TTTTTTATTTTTTAA	2177
rs768843179	snp	C/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091465	TGTCAGACTCAGACC[C/G]TGTCTCAAAAAGAAA	2177
rs768845755	snp	A/G	1.64827e-05	0.00287073	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092242	TCAGTATCCTCATCA[A/G]CTTGATAAAGGTGAG	2177
rs768851756	snp	A/G	1.65908e-05	0.00288012	missense	FANCD2	GRCh38.p7	3:10032838	TATTTTCAGAAACCA[A/G]GAAGCAACCACTTTC	2177
rs768853855	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10029327	TAACATAGCGAGACT[C/T]CATCTCTACAAAAAA	2177
rs768907834	snp	C/G	1.65034e-05	0.00287253	stop-gained	FANCD2	GRCh38.p7	3:10073319	CAGAAGAGAAAAATT[C/G]AGAATGTGACCCTAC	2177
rs768916596	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088971	GGAGTTCTTTCCTCC[A/G]GTTTTTCCCTTAAGA	2177
rs768934827	snp	A/G	3.31367e-05	0.00407029	synonymous-codon	FANCD2	GRCh38.p7	3:10043142	GTTGAAAAGTAAAGG[A/G]CGAGCAAGGTAAAGA	2177
rs768937298	snp	C/T	1.6591e-05	0.00288015	utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101285	ATAAATTGTTGCCTG[C/T]TTCTGTGTCTCTGCC	2177
rs768988673	snp	C/G/T	3.2948e-05	0.00405871	missense	FANCD2	GRCh38.p7	3:10078187	TTGCCAGGAGAGTCC[C/G/T]CTTTCTCAAGGTTAG	2177
rs768989374	snp	C/T	1.64958e-05	0.00287187	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098757	ATTCCCAGGAGAGCA[C/T]AGCAGATGAGAGTGA	2177
rs769008689	in-del	-/G			intron-variant	FANCD2	GRCh38.p7	3:10041481	AAAACAATTTTTAAA[-/G]AAACATACTATAAAC	2177
rs769115043	snp	C/T	6.61201e-05	0.00574941	missense	FANCD2	GRCh38.p7	3:10032918	AGCATCTTTGTAAAG[C/T]TTCTTAAGATATCAG	2177
rs769121339	in-del	-/GCATAGGACTTGG	1.64749e-05	0.00287005	intron-variant	FANCD2	GRCh38.p7	3:10078214	TTAGTGTAGGCAGAA[-/GCATAGGACTTGG]GCATAGTGGATTTGG	2177
rs769133104	snp	C/T	1.64749e-05	0.00287005	synonymous-codon	FANCD2	GRCh38.p7	3:10048006	TTCATTTGGCAGTCT[C/T]CTATACAAATATGCA	2177
rs769134549	in-del	-/T	1.65861e-05	0.00287972	intron-variant	FANCD2	GRCh38.p7	3:10064891	TCAGTATAGTTTTTC[-/T]TTTTCTAAACCTGTT	2177
rs769147120	snp	A/G	8.23635e-05	0.00641677	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085838	CTCAACCTGAAAATC[A/G]GAATTTACTGTATTC	2177
rs769150582	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10042058	ACCTGCCACCACTCC[C/T]GGCTAATTTTTGTAT	2177
rs769150639	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10060636	AAAATTAAGGATTGG[C/T]TAGAGGTAAAATTCT	2177
rs769153567	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10029205	CCAAGAGTTCCAGAT[A/G]TAAGGAGTTGATGGC	2177
rs769155337	snp	A/G	1.65321e-05	0.00287502	intron-variant	FANCD2	GRCh38.p7	3:10039875	TGTCATCATCTAAGT[A/G]AGGCTCAGCTATGGG	2177
rs769171665	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10080847	TTTTATGTGACCTTT[A/G]TCTGATTAGTTATGA	2177
rs769199393	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10043034	GAAAACCATAGCTAA[C/T]ATTTACTTTCTGCAG	2177
rs769200458	snp	A/G	4.94531e-05	0.00497234	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093287	TTCACCTCTCCAGGT[A/G]TTTGATAGTCATCCT	2177
rs769202819	snp	A/G	2.29603e-05	0.00338816	intron-variant	FANCD2	GRCh38.p7	3:10067351	ACTGGTAGTACTACT[A/G]GGCCAGTAGTGAGGC	2177
rs769220498	in-del	-/G			intron-variant	FANCD2	GRCh38.p7	3:10033810	GGTTCACACCATTCT[-/G]CCTCAGCTTCCCAAG	2177
rs769227516	snp	C/T	4.29775e-05	0.0046354	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087279	GGTGATGGGCCTAGA[C/T]CCTTTTTTTTTTTTT	2177
rs769239679	in-del	-/A			intron-variant	FANCD2	GRCh38.p7	3:10051871	GGTCACAAAGTAAAT[-/A]AGTTTCCTTGTGACT	2177
rs769263756	snp	A/G	0.000100817	0.00709917	intron-variant	FANCD2	GRCh38.p7	3:10043788	TAACGTGTTTCGCTG[A/G]TGTGTCATAATATTT	2177
rs769268545	snp	G/T	0.000527122	0.016226	missense	FANCD2	GRCh38.p7	3:10064392	TGTAATGATTTCCAG[G/T]ATGCCTTCGTAGTGG	2177
rs769322106	snp	C/T	1.67534e-05	0.0028942	intron-variant	FANCD2	GRCh38.p7	3:10062222	CACAGGTGAGTTCTT[C/T]TTTTCCTTTCTTTCT	2177
rs769329703	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10058781	AATCAGGAAGTGTGG[G/T]CCCTCCAACTTTGTT	2177
rs769332990	snp	A/G/T	4.96006e-05	0.00497978	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096304	AACTCACAAAAGATG[A/G/T]ATGTTATTTATTTCC	2177
rs769343757	snp	A/G	1.64754e-05	0.00287009	intron-variant	FANCD2	GRCh38.p7	3:10078072	CTAATCCTTTCCTCC[A/G]TGTGACAGGCTACAG	2177
rs769402896	snp	C/G	1.64749e-05	0.00287005	missense	FANCD2	GRCh38.p7	3:10039757	CAGCTGATCAGTATT[C/G]CTCCAGAGAACCTGC	2177
rs769459614	snp	C/T	0.000132959	0.00815241	intron-variant	FANCD2	GRCh38.p7	3:10049514	TGTAAAGGTATCTTA[C/T]TGGCTTCTTGTACTT	2177
rs769468648	snp	A/G	3.34219e-05	0.00408777	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101147	GAGGTCACCCAGAGC[A/G]GTAACCTAAAATGCT	2177
rs769503036	snp	A/C			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082208	AAACCAGGAGTTATT[A/C]TTTGTCCCTCCCTCT	2177
rs769523740	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10033887	TATTTTTAGTAGAGA[C/T]GGAGTTTCACCGTGT	2177
rs769539948	in-del	-/TT			intron-variant	FANCD2	GRCh38.p7	3:10030098	GGCCCATTATATCAT[-/TT]TTTTTTTTTTTTTTG	2177
rs769541872	in-del	-/CA	1.6808e-05	0.00289892	splice-acceptor-variant	FANCD2	GRCh38.p7	3:10065861	ATGTTTGTTCTCTCT[-/CA]GATTGTCCTATATTC	2177
rs769551237	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10056881	TGTTTTTGAGATGGG[G/T]TCTCACTCTGTCACA	2177
rs769569924	snp	C/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082896	CCTGACAAAAACTTT[C/G]AACAATTTATCAAAG	2177
rs769619477	snp	A/G	1.6507e-05	0.00287284	intron-variant	FANCD2	GRCh38.p7	3:10063945	TCTTAAAGCAATAAA[A/G]CATGAGAGCTGCTTT	2177
rs769631118	snp	A/G	1.64825e-05	0.00287071	intron-variant	FANCD2	GRCh38.p7	3:10042513	CAGTACAAAGTTGAG[A/G]TAGTGACATGAAAAC	2177
rs769652718	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083908	AAAAAAAAAAAAAAA[A/G]GTATGTCCACCAGGG	2177
rs769653085	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10076505	TGACAGAGCATAATA[C/G]CTATCCTTTATATGA	2177
rs769666326	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10037667	ATTGAAAAAGATTAC[C/T]CTTTAAAATAAAGAA	2177
rs769670126	snp	A/G	1.64727e-05	0.00286986	missense, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10081414	GGAGTACCACATAAT[A/G]TCTTCCTGCTATCAG	2177
rs769704068	snp	A/G	1.671e-05	0.00289045	splice-acceptor-variant, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095199	AACTTATTGGTTATA[A/G]GAAGATGTTCTGAGC	2177
rs769704819	in-del	-/A			intron-variant	FANCD2	GRCh38.p7	3:10044513	CTCTACTAAAAATAC[-/A]AAAAAAAATTAGCCT	2177
rs769712384	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10060859	ATCTAAAGAAATATC[G/T]GTTTGGGGGCTTGAT	2177
rs769718142	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10053884	TTTCTAAGAAACATC[C/T]CCATCTAATGTGAAC	2177
rs769718373	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10036509	TTTCATCTATTAATA[C/T]GACTTTGTAAAAATA	2177
rs769742252	snp	C/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082386	ACACTTGGCCTCTCT[C/G]AGTCCATTCTTCACA	2177
rs769771419	snp	A/G	0.000156646	0.00884863	intron-variant	FANCD2	GRCh38.p7	3:10034665	TAAACTAAAAATTTT[A/G]TTCTTTTTTATTTTT	2177
rs769784339	snp	G/T	3.6075e-05	0.00424691	intron-variant	FANCD2	GRCh38.p7	3:10046743	GTGTCAGAGACTATT[G/T]ATTTTTAATCTAAAA	2177
rs769811062	snp	C/G	3.40385e-05	0.0041253	missense	FANCD2	GRCh38.p7	3:10067256	TGAGATGAAGGGGAA[C/G]GTGCTCACTCGGTTA	2177
rs769813552	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10080710	CAGGAATTCAAGGCT[A/G]CAGTGAGCTGTGATC	2177
rs769831892	snp	C/G	1.64814e-05	0.00287061	missense	FANCD2	GRCh38.p7	3:10046682	CGATCAGGCTGCATT[C/G]AAGAACAGCTGCTCC	2177
rs769844392	snp	C/T	9.89511e-05	0.00703319	synonymous-codon	FANCD2	GRCh38.p7	3:10060335	GCAGCTCTCTAGCAC[C/T]GTATTCAAGTACAAG	2177
rs769846364	snp	G/T	1.64784e-05	0.00287035	intron-variant	FANCD2	GRCh38.p7	3:10065366	ACACCTATGAAGTGT[G/T]GTCTAGAAATTTATT	2177
rs769903320	snp	A/G	3.32734e-05	0.00407868	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090296	CCGTCTTCTAGGCAT[A/G]CTTTTGTTGTTTTCT	2177
rs769913433	snp	A/G			intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10099300	TTTTGTGGTACAGAT[A/G]CTTTCGACAATTTAA	2177
rs769931863	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10029199	AAGATCCCAAGAGTT[C/T]CAGATATAAGGAGTT	2177
rs769935037	snp	C/G	1.64732e-05	0.0028699	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088950	TCCCTACACTGACCA[C/G]GTAAGGGAGTTCTTT	2177
rs769939372	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10066204	TTTATTTTCTCCAAG[C/T]TGCCTTCTCCCTAGA	2177
rs769945632	snp	A/G	8.24056e-05	0.00641841	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098780	GAGAGTGAGGATGAC[A/G]TGTCATCCCAGGCCT	2177
rs769950147	snp	C/T	1.64732e-05	0.0028699	missense	FANCD2	GRCh38.p7	3:10064764	AAGCACTGTACGGAC[C/T]GGAAGAATACGACAC	2177
rs769972404	in-del	-/CCAGATGGTA			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026743	GGGCTTTTCTGGAAG[-/CCAGATGGTA]CCAGATGGTATCGCA	2177
rs770003791	snp	A/G	1.64901e-05	0.00287137	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085938	GTGAGTCATAACTAC[A/G]TAGCCAAGATTGTTG	2177
rs770047071	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100321	CTCTCATACTAGTAT[C/T]GTAAGCCAGACAGAA	2177
rs770051715	snp	A/C	1.64972e-05	0.00287199	missense	FANCD2	GRCh38.p7	3:10073342	GACCCTACGCCATCT[A/C]ATAGAGGCCAGCTAA	2177
rs770070362	snp	A/G	1.80029e-05	0.00300019	intron-variant	FANCD2	GRCh38.p7	3:10039242	TTATTTTGACCAGAA[A/G]GGCTCAGTTCCCTGT	2177
rs770115679	in-del	-/GATACACTT	1.64732e-05	0.0028699	cds-indel	FANCD2	GRCh38.p7	3:10042652	TCCGTAACAGCCATG[-/GATACACTT]GAGGTATGCTCTTAT	2177
rs770126131	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10050492	GCCGGGCATCGTGGC[A/G]GTCGCCTGTAGTCCC	2177
rs770137587	snp	A/T	1.84361e-05	0.00303607	intron-variant	FANCD2	GRCh38.p7	3:10065991	AGAGGTGAGCAGAGT[A/T]AATAGGATGTTTCAC	2177
rs770159002	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091051	GGCTAGCATAGGGAA[A/G]CAGAGAAGCTACAGC	2177
rs770165003	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10062510	GCCTCCCAAAGTGCT[G/T]GGAGTACAGGCGTGA	2177
rs770205838	in-del	-/GCTT	1.93996e-05	0.00311439	intron-variant	FANCD2	GRCh38.p7	3:10046765	AATCTAAAACAGAAA[-/GCTT]TACAGCTCTCATGTA	2177
rs770226964	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10049256	GATAATAGGTGATGG[A/G]TTTGGGTTGATTGTG	2177
rs770231582	snp	A/G	1.64822e-05	0.00287068	missense	FANCD2	GRCh38.p7	3:10063859	CCTCTGCACTTTACT[A/G]TGATGAATTTGCCAA	2177
rs770240360	in-del	-/AG	1.68707e-05	0.00290432	intron-variant	FANCD2	GRCh38.p7	3:10035152	AGCAAAGTGGAAAAC[-/AG]ATTTCTTTTTTTTTT	2177
rs770270765	snp	G/T	4.94434e-05	0.00497184	intron-variant	FANCD2	GRCh38.p7	3:10063780	TTAAACCATTCTTCC[G/T]CTTTGCTCCAGGTGA	2177
rs770327387	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10053477	GCACATGTATACATA[C/T]GTAACTAACCTGCAC	2177
rs770393574	in-del	-/TTTTTTT			intron-variant	FANCD2	GRCh38.p7	3:10046055	TATTGCTCTGTATTC[-/TTTTTTT]TTTTTTTTTTTTTTT	2177
rs770398576	snp	C/T	1.65737e-05	0.00287864	intron-variant	FANCD2	GRCh38.p7	3:10039887	AGTGAGGCTCAGCTA[C/T]GGGGGTTCTATCACT	2177
rs770421515	snp	G/T	1.6486e-05	0.00287102	missense	FANCD2	GRCh38.p7	3:10052414	TATCTGGATAACATA[G/T]CCCCTCAGCAAATAC	2177
rs770442271	snp	G/T	6.59609e-05	0.00574248	missense	FANCD2	GRCh38.p7	3:10046585	TTGACAATAGGTGTT[G/T]GACCTGGTGATGCTT	2177
rs770447063	snp	C/G	1.64749e-05	0.00287005	stop-gained	FANCD2	GRCh38.p7	3:10048012	TGGCAGTCTCCTATA[C/G]AAATATGCATTTAAG	2177
rs770454845	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081939	GCCCCTTAAATACTT[C/T]TGTTCCTCAGGGACA	2177
rs770464737	snp	C/G	1.65059e-05	0.00287275	missense	FANCD2	GRCh38.p7	3:10065908	CCTGGAGAGAAGTTG[C/G]AGTCCATGTCTGCTA	2177
rs770473878	snp	A/C	1.67584e-05	0.00289464	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088571	TTTCTTCCAATGAGC[A/C]AAATAGCTTTTTTCT	2177
rs770482835	snp	G/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095167	ATGAAATCAGGACAT[G/T]TCATAGAGCATTTAT	2177
rs770511441	snp	A/C	1.76705e-05	0.00297236	intron-variant	FANCD2	GRCh38.p7	3:10043898	GCATTTTCAGTATTG[A/C]AGACTTAAAAGTAAT	2177
rs770526431	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10075276	GCAAGCTCTGCCTCC[C/T]GGGTTCACGCCATTC	2177
rs770610141	snp	A/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10080940	GGAAGATGGAGCAAG[A/T]TTTTTATCCCTCTGT	2177
rs770626548	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094264	ATACCTCAGCTAGAG[A/G]TAACAGTGTGTCTCT	2177
rs770654896	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10060767	TGTGTCATTCCTGTC[A/G]GGAACTTTATACATT	2177
rs770674504	snp	A/G			intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10099170	GAGTTAAACCATTTA[A/G]ACACATTTGAAACAT	2177
rs770686014	in-del	-/AG			frameshift-variant, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085886	GTAGCCGACTGAAAC[-/AG]GGAGAACACAGCCAG	2177
rs770697903	snp	A/G	6.60971e-05	0.00574841	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096314	AGATGGATGTTATTT[A/G]TTTCCATTCAGATTC	2177
rs770744945	snp	A/G	1.66654e-05	0.00288659	intron-variant	FANCD2	GRCh38.p7	3:10049535	TCTTGTACTTTAGAT[A/G]TTGAATACTATAATT	2177
rs770768796	snp	A/G	1.64879e-05	0.00287118	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096492	GCCTTGGATCCTGCT[A/G]GTGATAATCCCCTAC	2177
rs770769534	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10049657	CACTTCTTTATACCT[A/T]ACCTACAGGCTAATC	2177
rs770808744	in-del	-/A	1.64982e-05	0.00287208	frameshift-variant	FANCD2	GRCh38.p7	3:10072899	TGTCCCTCCTCTTGG[-/A]AACTTTGATGTGGAA	2177
rs770811893	in-del	-/CTT			intron-variant	FANCD2	GRCh38.p7	3:10041241	CAATCTATCACTGTC[-/CTT]CTCACTATGTTGTGC	2177
rs770833290	snp	A/G	1.64749e-05	0.00287005	intron-variant	FANCD2	GRCh38.p7	3:10064475	CACTGGTGAAGTTAC[A/G]TCAATTCTGTCAGTA	2177
rs770835633	in-del	-/A	1.64928e-05	0.00287161	frameshift-variant	FANCD2	GRCh38.p7	3:10034490	ATCAAATAGCTTTCC[-/A]AAAGAAGCTCTTTCA	2177
rs770854100	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087689	GTCTCGTTCTGTCAC[C/T]CAGGCTGGAGTGCAG	2177
rs770863196	snp	G/T			missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090385	AGCAGACTCGCAGCA[G/T]GTGAGTAAGATAATA	2177
rs770916832	snp	A/G	1.64738e-05	0.00286995	intron-variant	FANCD2	GRCh38.p7	3:10042676	GAGGTATGCTCTTAT[A/G]TCCCATCACACCTAG	2177
rs770921753	in-del	-/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092432	TTTCTCACTAGGCAT[-/T]TTTTTTTTTTGTCTT	2177
rs770937751	snp	A/G	1.65012e-05	0.00287234	intron-variant	FANCD2	GRCh38.p7	3:10067368	GCCAGTAGTGAGGCA[A/G]TAAAGCACTTAGCTT	2177
rs770946439	snp	A/G			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027241	GCCCCAGTCTAGTGT[A/G]AGGTAAGGGCCCCTA	2177
rs770971003	snp	A/G	3.3325e-05	0.00408184	missense	FANCD2	GRCh38.p7	3:10062164	AGAAGTGAATCACCT[A/G]GTTTGACCCAAGAGA	2177
rs770985541	snp	A/G	0.000115309	0.00759218	missense	FANCD2	GRCh38.p7	3:10042592	GATAAGTTGTCGTCT[A/G]TTAGATTGGAGGATT	2177
rs771059153	snp	A/G	3.29462e-05	0.00405857	missense, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10081440	ATCAGAGGCTGCTGC[A/G]GATTTTTCATGGGCT	2177
rs771062648	snp	C/T	1.64741e-05	0.00286998	missense	FANCD2	GRCh38.p7	3:10047942	ATATGTGTTCATCCA[C/T]TCTGTCGCTGGCTCA	2177
rs771078251	snp	C/T	1.65976e-05	0.00288072	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090314	TTTGTTGTTTTCTTC[C/T]GTGTGATGATGGCTG	2177
rs771088798	snp	A/C	4.94474e-05	0.00497205	missense	FANCD2	GRCh38.p7	3:10028707	ATAAAGAGAGCCTGA[A/C]AGAAGATGCCTCCAG	2177
rs771122987	snp	C/T	1.64738e-05	0.00286995	intron-variant	FANCD2	GRCh38.p7	3:10065383	TCTAGAAATTTATTT[C/T]TCCTTCTCAGATTGG	2177
rs771157552	snp	A/G			downstream-variant-500B, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10102095	CTTCATCTGAGATGA[A/G]ATATATCTGATCTTT	2177
rs771173054	snp	A/G	1.70336e-05	0.00291831	intron-variant	FANCD2	GRCh38.p7	3:10060430	GATTCTGACTTCTGT[A/G]GTTTAAGATCAGTTA	2177
rs771173455	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097805	AATCTTTACAATTTA[C/T]GTTTAGAGATTACAG	2177
rs771192148	snp	A/T	3.30447e-05	0.00406464	missense	FANCD2	GRCh38.p7	3:10064856	GGGGGTCCGGTGACC[A/T]CACAGGAATCAGGCC	2177
rs771220579	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10071536	ATCCTGTTGTTTGCA[A/G]CAATACAGATGGAAC	2177
rs771260001	in-del	-/AAA	6.61272e-05	0.00574971	intron-variant	FANCD2	GRCh38.p7	3:10048091	AAGGAGGGAACACAG[-/AAA]GGGAAAATAATCTGA	2177
rs771269835	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10032392	CTCAAGTTATTCTTC[C/T]GCCTTAGCCTCCGAA	2177
rs771272539	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10066126	CCCACCACTCCCCAG[G/T]TATATGAACCTCCTT	2177
rs771323964	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10065243	GCAGTGAGCTGAGAT[C/G]GTGCCACTGCACTCC	2177
rs771359822	snp	A/G	1.64727e-05	0.00286986	missense	FANCD2	GRCh38.p7	3:10049399	GTGCCTTAGTGACCC[A/G]TATCTGCAGTGGGAA	2177
rs771360992	snp	C/T	3.29875e-05	0.00406112	intron-variant	FANCD2	GRCh38.p7	3:10063929	AAAGCCAATTGTCTT[C/T]TCTTAAAGCAATAAA	2177
rs771363146	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10044754	AAAGCAATGAAAATT[A/C]AGAATTTTTTCTGGT	2177
rs771375235	snp	A/G	0.000255443	0.0112985	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087255	TCTGCTCAGAACAAA[A/G]AAAAAATTGGTGATG	2177
rs771386311	snp	A/G	0.000407879	0.0142749	intron-variant	FANCD2	GRCh38.p7	3:10074515	ATTCTCTTTGTTGCT[A/G]TGACTTCCCCATAGG	2177
rs771387451	snp	C/T	1.65529e-05	0.00287683	missense	FANCD2	GRCh38.p7	3:10043518	AGCAGCGGTCAGAGC[C/T]GTATTATTCTCCTCT	2177
rs771398282	in-del	-/C	1.65059e-05	0.00287275	frameshift-variant	FANCD2	GRCh38.p7	3:10043079	CGGGAGAAGTTGGAT[-/C]CTGCAGCATTGTGTT	2177
rs771401180	snp	C/G/T	6.61861e-05	0.00575233	intron-variant	FANCD2	GRCh38.p7	3:10048095	AGGGAACACAGAAAG[C/G/T]GAAAATAATCTGATG	2177
rs771410260	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10039515	ATCATAGATACTTCA[C/T]CCTTTAAATTTCAGA	2177
rs771414227	snp	C/G	1.64738e-05	0.00286995	intron-variant, missense	FANCD2, FANCD2OS	GRCh38.p7	3:10098906	ACTTTGCCTACTTAT[C/G]TTTATTGTCAAATGC	2177
rs771445756	snp	A/G/T	0.000330876	0.0128588	synonymous-codon	FANCD2	GRCh38.p7	3:10032950	AATTATTCTTAAAAC[A/G/T]GGAGAGAGTCAGAAT	2177
rs771454092	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10057431	GTGCAGTGGCACAAT[A/C]TCAGCTCACTCCAAC	2177
rs771466741	snp	C/G	1.64743e-05	0.00287	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087143	TTACAGCCAGAGCGT[C/G]CATTACTTGCAGAAT	2177
rs771566720	snp	G/T	1.65321e-05	0.00287502	intron-variant	FANCD2	GRCh38.p7	3:10041748	GAAACAGAGCCAGCT[G/T]TCCAACCTCCCAGAA	2177
rs771573600	snp	A/T	1.65078e-05	0.00287291	splice-acceptor-variant	FANCD2	GRCh38.p7	3:10034467	TTCTTTTTTCTGCAT[A/T]GCTGTGGATCAAATA	2177
rs771593345	snp	C/T	3.29734e-05	0.00406025	missense	FANCD2	GRCh38.p7	3:10063871	ACTATGATGAATTTG[C/T]CAACCTGATCCAACA	2177
rs771646919	snp	C/T	1.64817e-05	0.00287064	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093341	GAGAGATTTACTGGG[C/T]CCTGTTTCATATTTA	2177
rs771698231	snp	C/T	3.2962e-05	0.00405954	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093306	GATAGTCATCCTGTT[C/T]TGCATGTATGTTTGA	2177
rs771721585	in-del	-/GTGA	1.77313e-05	0.00297747	splice-donor-variant, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090386	GCAGACTCGCAGCAG[-/GTGA]GTAAGATAATAGTCA	2177
rs771778790	in-del	-/AA			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10028052	ACCCTGTCTCTACTA[-/AA]AAAAAAAAAAAAAAA	2177
rs771839228	snp	A/G	1.64741e-05	0.00286998	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094333	GAAGCAATGTATGCC[A/G]CTCCTAGACTTCAGT	2177
rs771846214	snp	A/G	1.64738e-05	0.00286995	intron-variant	FANCD2	GRCh38.p7	3:10064684	TTTCCCTGTAGCCTT[A/G]CGTATTCCTGAGCTG	2177
rs771855724	snp	A/G	1.64754e-05	0.00287009	intron-variant	FANCD2	GRCh38.p7	3:10078229	GCATAGGACTTGGGC[A/G]TAGTGGATTTGGGAA	2177
rs771863155	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10045971	CTGGAGTTGGCAAGT[C/G]ATTGAATCTTTCTTT	2177
rs771869385	snp	C/T	6.59044e-05	0.00574002	stop-gained	FANCD2	GRCh38.p7	3:10046667	CTAAGAAATAAGATT[C/T]GATCAGGCTGCATTC	2177
rs771879222	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10062452	TCACCATGTTGGCCC[C/T]GCTGGTCCTGAACTC	2177
rs771903324	snp	A/G	1.64727e-05	0.00286986	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088905	TCCCAGAACTGATCA[A/G]CTCTCCTAAAGATGC	2177
rs771918164	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10065212	GATAATTGCTTGAAC[C/T]TGGGAGGCAGAGGTT	2177
rs771935846	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10064247	ATTTATTATTACTTT[C/T]TTTTTAGAAATGAGG	2177
rs771941551	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10038332	TAGCTAAATGTCTCA[C/T]GCTGGATGCTTTACA	2177
rs771967363	snp	C/T			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026965	GGTGAAGAGCGCAGG[C/T]GCTGAAGCCAGACTC	2177
rs771967812	snp	A/T	3.3399e-05	0.00408637	intron-variant	FANCD2	GRCh38.p7	3:10052519	GGCAATATGTTGGGA[A/T]AGATTTTTTTTTTTT	2177
rs771969488	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086460	CAGCAGTCAGTGCTT[A/G]TCATCCCTGTCTATA	2177
rs771978225	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10032730	TCCTAGTATAATTTT[C/T]AAGGACACATCAGTT	2177
rs771985778	snp	A/T	1.65471e-05	0.00287633	missense	FANCD2	GRCh38.p7	3:10073276	CAAAAAACAGATGGC[A/T]GCAAGACATCCTCCT	2177
rs771989089	in-del	-/CCTCTC			intron-variant	FANCD2	GRCh38.p7	3:10069460	ACCCTAGTTAAGATG[-/CCTCTC]CCCCTCCCCCTCCCC	2177
rs771998947	snp	C/T	1.64849e-05	0.00287092	intron-variant	FANCD2	GRCh38.p7	3:10036284	CTATGTCTTCTTTTT[C/T]AGCCTGCCATTATCA	2177
rs772006962	snp	A/C			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098289	CCGGAGTTTGAGTCC[A/C]AACAGTCCCAAATCC	2177
rs772017887	snp	C/T	1.64743e-05	0.00287	missense	FANCD2	GRCh38.p7	3:10047996	AGAGTATAATTTCAT[C/T]TGGCAGTCTCCTATA	2177
rs772026036	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10071614	ACATATTTGTGGGAG[C/T]TGAAAATTAAAATAA	2177
rs772029723	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10036753	GAAGGATACACAATA[C/T]ACTGGTAATGGTAGT	2177
rs772038476	snp	A/G	5.00013e-05	0.00499981	synonymous-codon	FANCD2	GRCh38.p7	3:10072953	TGTTACTGCTATTTC[A/G]GCAAAAATCAGAAAG	2177
rs772055664	snp	C/G	1.6486e-05	0.00287102	missense	FANCD2	GRCh38.p7	3:10046589	CAATAGGTGTTTGAC[C/G]TGGTGATGCTTTTCA	2177
rs772075763	snp	C/T	9.8837e-05	0.00702914	synonymous-codon	FANCD2	GRCh38.p7	3:10064735	TCTCCGCAGTGACTT[C/T]CCATTTCCTGTGAAA	2177
rs772092834	snp	A/C	1.64735e-05	0.00286993	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085828	AGTGGATTTTCTCAA[A/C]CTGAAAATCAGAATT	2177
rs772113237	snp	G/T	1.64749e-05	0.00287005	intron-variant	FANCD2	GRCh38.p7	3:10042702	CCTAGATAAAGCAAC[G/T]TAAGTGCCAATTGCT	2177
rs772162757	snp	C/G			upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025894	TCCCCATTTCACAGA[C/G]GACAAAAGTGAAACA	2177
rs772163949	snp	C/T	1.64825e-05	0.00287071	missense	FANCD2	GRCh38.p7	3:10052439	AAATACGAAAACTCT[C/T]CTATGTTCTCAGCAC	2177
rs772169028	snp	A/G	3.29843e-05	0.00406092	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096335	ATTCAGATTCACCAG[A/G]ACACGAGACTCACCC	2177
rs772173673	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10042224	TTAAGCAGTAAGTTT[G/T]GAGTGGAAATCTTCC	2177
rs772180708	snp	A/G	4.94303e-05	0.00497119	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092221	GGAACATGGCTGTTC[A/G]AGACTTCAGTATCCT	2177
rs772200129	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10037913	TAATAGTGTACCTTT[C/T]TGGAATGACAGGATT	2177
rs772201181	snp	G/T	3.29576e-05	0.00405928	missense	FANCD2	GRCh38.p7	3:10035177	TTTTTTTACAGTATG[G/T]GTGCATCTTATTCTA	2177
rs772237103	snp	A/C	1.64743e-05	0.00287	missense, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10081461	TTCATGGGCTTTTTG[A/C]TTGGTAAGTATGTGG	2177
rs772259116	snp	A/G	1.65605e-05	0.0028775	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10099000	AAGAAACAACGACAC[A/G]ATCTTAGAATCACTC	2177
rs772263587	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10068741	CATTACCTGACTTCA[A/G]ATTATACTACAGAGC	2177
rs772281705	snp	A/C/T	4.94224e-05	0.00497083	synonymous-codon	FANCD2	GRCh38.p7	3:10039750	GATCATGCAGCTGAT[A/C/T]AGTATTGCTCCAGAG	2177
rs772307876	snp	A/G	1.73192e-05	0.00294267	intron-variant	FANCD2	GRCh38.p7	3:10060446	GTTTAAGATCAGTTA[A/G]TCTTGCTAACTAAGT	2177
rs772312489	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10040374	ATACCTGTTATGAGC[A/G]TGAAGTCTGGCTTAG	2177
rs772315142	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10089207	GGAGAATTGCTTGAA[C/T]CTGGGAGGCGGAGGT	2177
rs772349916	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10077715	CAACAAAGTGAGACC[C/T]CGTCTGTATAAAAAA	2177
rs772367491	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082003	TTCTGGTCAATCCTA[C/T]CCAAGCTTAAATTTA	2177
rs772418552	snp	C/T	1.66957e-05	0.00288922	intron-variant	FANCD2	GRCh38.p7	3:10032809	ACTATTTGCCATATT[C/T]TTGAAAATTTTTCTA	2177
rs772428199	in-del	-/GTCTTTGTA	1.66211e-05	0.00288275	cds-indel	FANCD2	GRCh38.p7	3:10049478	TTAAACCCATCTGCT[-/GTCTTTGTA]ATGATGATGAATGCT	2177
rs772442959	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090650	TTTTTAGTAGAGACA[A/G]GGTTTCACCATGTTG	2177
rs772472783	snp	C/T	0.000117721	0.00767116	intron-variant	FANCD2	GRCh38.p7	3:10043639	GGAAATGAGTGGCAA[C/T]TAGTGACAGATGTAT	2177
rs772531991	snp	A/T	3.29506e-05	0.00405884	intron-variant	FANCD2	GRCh38.p7	3:10078075	ATCCTTTCCTCCATG[A/T]GACAGGCTACAGAAG	2177
rs772533024	snp	C/T	3.30164e-05	0.00406289	intron-variant	FANCD2	GRCh38.p7	3:10039866	TAAACCCTCTGTCAT[C/T]ATCTAAGTGAGGCTC	2177
rs772558102	snp	A/G	5.65456e-05	0.00531692	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090417	TCACTTCAAGAAGTG[A/G]ACTTTGGATTACTTG	2177
rs772565209	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10044893	AATATAATTTGTATT[C/G]TTACTTTTTTTTCTT	2177
rs772582526	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093970	AGCTTTACCCAGTTT[C/T]TCCCTCTTGGGAGTA	2177
rs772610095	snp	A/G	1.64958e-05	0.00287187	intron-variant	FANCD2	GRCh38.p7	3:10028732	CTCCAGTAAGTATCT[A/G]GTCATTTGTTGCTTT	2177
rs772618957	snp	C/G	1.64814e-05	0.00287061	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101257	AGTTATGATGACTCT[C/G]ATTAGACCCCAGATA	2177
rs772621573	snp	A/G	1.64743e-05	0.00287	intron-variant	FANCD2	GRCh38.p7	3:10065500	GGTCTACTAGGTATG[A/G]GATGAAGTCATCAGA	2177
rs772656979	snp	C/T	1.64762e-05	0.00287016	missense	FANCD2	GRCh38.p7	3:10074636	TACATTGTGGACTTG[C/T]GACGAAGTTCATCTT	2177
rs772659791	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082749	TCTCTTCTAACACTC[C/T]GGTATCCGTTCGTGA	2177
rs772679313	in-del	-/AT	1.71223e-05	0.00292589	frameshift-variant	FANCD2	GRCh38.p7	3:10067235	CTTCTGCCAGGAAAC[-/AT]CACCTGAGATGAAGG	2177
rs772693410	snp	A/G	1.64735e-05	0.00286993	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092155	TGGCTGTGACTCAGA[A/G]GTGCCCATATATTTG	2177
rs772705094	snp	A/G	1.74647e-05	0.002955	intron-variant	FANCD2	GRCh38.p7	3:10043885	GTTCATGTACTATGC[A/G]TTTTCAGTATTGCAG	2177
rs772745065	snp	A/C/G	4.94347e-05	0.00497145	intron-variant	FANCD2	GRCh38.p7	3:10078056	TAGGACATTCCTGGA[A/C/G]CTAATCCTTTCCTCC	2177
rs772783243	snp	A/G	1.66863e-05	0.0028884	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101151	TCACCCAGAGCAGTA[A/G]CCTAAAATGCTTATT	2177
rs772815874	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083660	TTGGGAGGCCGAGGC[A/G]GGCAGATCATGAGGT	2177
rs772828881	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10057978	TGACCAATTATTACT[C/T]ATTAGTAGCTTTTTT	2177
rs772882515	snp	C/T	1.66208e-05	0.00288273	intron-variant	FANCD2	GRCh38.p7	3:10049515	GTAAAGGTATCTTAT[C/T]GGCTTCTTGTACTTT	2177
rs772906829	snp	A/G	1.64789e-05	0.0028704	missense	FANCD2	GRCh38.p7	3:10074656	AAGTTCATCTTAGAT[A/G]CTGAAATGCACACTG	2177
rs772924767	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098325	TGATGTTCTGAAACC[A/G]CCTCACCATACTGTC	2177
rs772982872	snp	A/G	3.61265e-05	0.00424994	intron-variant	FANCD2	GRCh38.p7	3:10046744	TGTCAGAGACTATTG[A/G]TTTTTAATCTAAAAC	2177
rs773070332	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10041015	CCTGGACAACATGGT[A/G]AAAAGCCGTCTTTCA	2177
rs773072936	snp	A/G/T	6.58939e-05	0.00573962	synonymous-codon	FANCD2	GRCh38.p7	3:10042588	GATGGATAAGTTGTC[A/G/T]TCTATTAGATTGGAG	2177
rs773074211	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10035109	CAATTTTATTGAGAA[A/G]AGATGATAAAAGCAT	2177
rs773077438	snp	A/G	1.64732e-05	0.0028699	missense	FANCD2	GRCh38.p7	3:10064393	GTAATGATTTCCAGG[A/G]TGCCTTCGTAGTGGA	2177
rs773091344	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101024	CAGTGAGCTGAGATC[A/G]TGCCACTGCATTCCA	2177
rs773095325	snp	A/C	1.65718e-05	0.00287848	intron-variant	FANCD2	GRCh38.p7	3:10063961	CATGAGAGCTGCTTT[A/C]CTACACTCTTCAAGT	2177
rs773122720	in-del	-/T/TT	0.100381	0.20433	intron-variant	FANCD2	GRCh38.p7	3:10062247	TTTCTTTTTCCTGTC[-/T/TT]TTTTTTTTTTTTTTA	2177
rs773134332	snp	C/G			upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10024521	GGGAGGCTGAGATGG[C/G]AGGATCCCTTGAGCC	2177
rs773138169	snp	A/T	6.18487e-05	0.00556062	intron-variant	FANCD2	GRCh38.p7	3:10034669	CTAAAAATTTTATTC[A/T]TTTTTATTTTTTAAA	2177
rs773153096	snp	A/G	1.64817e-05	0.00287064	intron-variant	FANCD2	GRCh38.p7	3:10042515	GTACAAAGTTGAGGT[A/G]GTGACATGAAAACCT	2177
rs773182166	snp	A/G	1.6664e-05	0.00288647	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095204	ATTGGTTATAGGAAG[A/G]TGTTCTGAGCTTACT	2177
rs773206371	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10038510	TTTCTTTATTTATAA[A/G]TGATTTTTAGTACTT	2177
rs773236503	in-del	-/GCATGATGATAAACTCACAAAAGATGGAT	1.65493e-05	0.00287652	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096278	ATAAGAAATGTGAAG[lengthTooLong]GTTATTTATTTCCAT	2177
rs773243852	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10039150	TGTGTGTCTAGTGCA[A/G]TGCCGAATGCATAGT	2177
rs773259037	snp	C/G	1.79819e-05	0.00299844	intron-variant	FANCD2	GRCh38.p7	3:10039244	ATTTTGACCAGAAAG[C/G]CTCAGTTCCCTGTTT	2177
rs773262142	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10065235	CAGAGGTTGCAGTGA[A/G]CTGAGATCGTGCCAC	2177
rs773297233	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10044698	TAGTTTTGTTATCCA[A/G]TTTTGGGATGATTAT	2177
rs773320606	snp	A/G	1.6492e-05	0.00287154	synonymous-codon	FANCD2	GRCh38.p7	3:10034494	AATAGCTTTCCAAAA[A/G]AAGCTCTTTCAGACC	2177
rs773341870	snp	A/G	1.64741e-05	0.00286998	intron-variant, missense	FANCD2, FANCD2OS	GRCh38.p7	3:10098900	AGCAGAACTTTGCCT[A/G]CTTATGTTTATTGTC	2177
rs773365252	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10077102	GCCAGGCATGGTGAC[A/G]CACACCTGTGATCCC	2177
rs773393305	snp	A/T	1.7625e-05	0.00296854	intron-variant	FANCD2	GRCh38.p7	3:10060249	CATACCTTCTTTTGC[A/T]GTGCCATTCCAGCAT	2177
rs773393663	snp	A/G	1.6516e-05	0.00287362	missense	FANCD2	GRCh38.p7	3:10064853	GATGGGGGTCCGGTG[A/G]CCTCACAGGAATCAG	2177
rs773483393	snp	A/G	1.64904e-05	0.00287139	missense	FANCD2	GRCh38.p7	3:10060336	CAGCTCTCTAGCACC[A/G]TATTCAAGTACAAGC	2177
rs773490965	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10063003	ACCACTCCCAGGCCA[C/G]TTGCATTTATTTCTA	2177
rs773525589	snp	C/T	1.7227e-05	0.00293482	intron-variant	FANCD2	GRCh38.p7	3:10039372	GGTAGGCTTATGGAC[C/T]TTATCTCTTGAATTT	2177
rs773534988	snp	C/T	1.64841e-05	0.00287085	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081310	AAATGAGGACAATTA[C/T]TGAAGCAACTGTCCT	2177
rs773539910	snp	A/G			upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025939	AAGGTCACCTTGCCA[A/G]TGGGGGCGAGACGTG	2177
rs773540135	snp	C/T	1.66316e-05	0.00288367	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090297	CGTCTTCTAGGCATA[C/T]TTTTGTTGTTTTCTT	2177
rs773562517	snp	A/G	1.64955e-05	0.00287184	missense	FANCD2	GRCh38.p7	3:10073348	ACGCCATCTCATAGA[A/G]GCCAGCTAAACAAGG	2177
rs773582349	in-del	-/A			intron-variant	FANCD2	GRCh38.p7	3:10068788	GCATGGTGCTGGCAC[-/A]AAAACAGATGCATAT	2177
rs773593671	snp	A/G	0.000230601	0.0107353	synonymous-codon	FANCD2	GRCh38.p7	3:10064765	AGCACTGTACGGACT[A/G]GAAGAATACGACACT	2177
rs773617787	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100479	CGAGTTCAAGCAATT[C/T]TCCTGCCTCAGCCTT	2177
rs773625038	snp	C/G	1.64852e-05	0.00287094	synonymous-codon, downstream-variant-500B	FANCD2, FANCD2OS	GRCh38.p7	3:10081135	TGGATTCTCACATCT[C/G]CAACAGAGATCTGCC	2177
rs773636192	snp	A/G	1.64909e-05	0.00287144	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085940	GAGTCATAACTACAT[A/G]GCCAAGATTGTTGTC	2177
rs773639853	snp	A/G			downstream-variant-500B, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10102066	AAAATCATGTCTCCT[A/G]TTGTAAGAACCAACT	2177
rs773656868	snp	C/T	1.65397e-05	0.00287569	missense	FANCD2	GRCh38.p7	3:10032942	ATATCAGGAATTATT[C/T]TTAAAACGGGAGAGA	2177
rs773660610	snp	A/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082093	TTAGATGTGGCATTG[A/T]CACCTCACACTCCAC	2177
rs773714983	snp	G/T	1.7345e-05	0.00294486	intron-variant	FANCD2	GRCh38.p7	3:10043444	TAAGTTCTTTTCTGG[G/T]ACGTAGAAGAGTAAT	2177
rs773716319	in-del	-/TTTT			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090444	CTTGGAAGTTGCTGA[-/TTTT]TTTTTTTTTTTTTTT	2177
rs773727330	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10032429	GGGACTACAGGTGTG[C/T]GTCTCCTCACCTAAC	2177
rs773734434	snp	A/G	0.000148337	0.00861085	missense	FANCD2	GRCh38.p7	3:10063864	GCACTTTACTATGAT[A/G]AATTTGCCAACCTGA	2177
rs773749486	in-del	-/A	1.69427e-05	0.00291051	intron-variant	FANCD2	GRCh38.p7	3:10043000	GACTGGACTGTGCCT[-/A]ACCCACTATGAATGA	2177
rs773754152	snp	C/T	1.64822e-05	0.00287068	intron-variant	FANCD2	GRCh38.p7	3:10063784	ACCATTCTTCCTCTT[C/T]GCTCCAGGTGACCTC	2177
rs773763827	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10029760	TCTCTTGAGTATCCA[A/G]AGTCCATTATATCAT	2177
rs773789154	in-del	-/AG			intron-variant	FANCD2	GRCh38.p7	3:10078016	TTTAACAAAAAAGAA[-/AG]AAAAAAAATTATCAT	2177
rs773823204	snp	C/T	4.9423e-05	0.00497082	synonymous-codon	FANCD2	GRCh38.p7	3:10048018	TCTCCTATACAAATA[C/T]GCATTTAAGTTTTTT	2177
rs773833838	snp	C/T	8.23662e-05	0.00641688	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085863	GTATTCAGCCCTCCA[C/T]GTCCTTAGTAGCCGA	2177
rs773847165	snp	A/T	1.65408e-05	0.00287578	missense	FANCD2	GRCh38.p7	3:10032870	AAAAAGACAAAGAAA[A/T]CTCATATTGCTAATG	2177
rs773911257	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10048090	CAAGGAGGGAACACA[A/G]AAAGGGAAAATAATC	2177
rs773939743	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10074321	AGATGACCTGTTAAG[A/G]GTCTTGATGTGTGAC	2177
rs773944524	snp	C/T	1.6507e-05	0.00287284	missense	FANCD2	GRCh38.p7	3:10065915	AGAAGTTGGAGTCCA[C/T]GTCTGCTAAAGAGCG	2177
rs773944694	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083321	TTAAAATAAATACAT[A/G]AAAGGATGTTTATTA	2177
rs773984853	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10071711	GACTGGGAAAAATGA[A/G]GGTGGTTAATAGCTT	2177
rs774013442	snp	G/T	0.028177	0.115302	intron-variant	FANCD2	GRCh38.p7	3:10043903	TTCAGTATTGCAGAC[G/T]TAAAAGTAATGACAT	2177
rs774013820	snp	C/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095578	CTAGGTAACAGGACT[C/G]TGATGTAAGTGATGA	2177
rs774017874	snp	G/T	1.65048e-05	0.00287265	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096327	TTATTTCCATTCAGA[G/T]TCACCAGGACACGAG	2177
rs774028340	snp	C/T	3.33979e-05	0.0040863	intron-variant	FANCD2	GRCh38.p7	3:10043814	TATTTTTGTGACTCT[C/T]TCCTGTTTTTTCAGG	2177
rs774035083	snp	A/G/T	4.94306e-05	0.00497124	intron-variant	FANCD2	GRCh38.p7	3:10065510	GTATGGGATGAAGTC[A/G/T]TCAGATCCTTTCTTC	2177
rs774040846	snp	C/T	3.32248e-05	0.0040757	intron-variant	FANCD2	GRCh38.p7	3:10039896	CAGCTATGGGGGTTC[C/T]ATCACTGCAGTATGC	2177
rs774077678	in-del	-/A			intron-variant	FANCD2	GRCh38.p7	3:10059586	GACAGGCGGATCACG[-/A]GGTCAGGAGATCGAG	2177
rs774102652	snp	A/G	1.64811e-05	0.00287059	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093316	CTGTTCTGCATGTAT[A/G]TTTGAAGGTGAGAGA	2177
rs774165755	snp	G/T	1.64743e-05	0.00287	missense	FANCD2	GRCh38.p7	3:10078094	AGGCTACAGAAGTTG[G/T]GCAACTTGGGCCCCC	2177
rs774194804	snp	C/T	1.64895e-05	0.00287132	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092258	CTTGATAAAGGTGAG[C/T]ATGGAGACTGCTTGA	2177
rs774200334	snp	C/T			synonymous-codon, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10081348	TTTTTATTTTTAGTG[C/T]TTAGCTGCTGAGAAT	2177
rs774220215	snp	G/T	1.66638e-05	0.00288645	intron-variant	FANCD2	GRCh38.p7	3:10049537	TTGTACTTTAGATAT[G/T]GAATACTATAATTGG	2177
rs774220567	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10031567	AAATGGCATCATTAA[G/T]GGAGAAGAGTAAATT	2177
rs774226785	snp	C/G	1.64743e-05	0.00287	intron-variant	FANCD2	GRCh38.p7	3:10042683	GCTCTTATATCCCAT[C/G]ACACCTAGATAAAGC	2177
rs774237163	snp	C/G	1.6825e-05	0.00290038	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088577	CCAATGAGCCAAATA[C/G]CTTTTTTCTATTTTG	2177
rs774299094	snp	A/G	1.66785e-05	0.00288773	missense	FANCD2	GRCh38.p7	3:10034731	GGCCTGGAGTCTTAC[A/G]TTGAGGATGAAGACA	2177
rs774301461	snp	C/T	1.64857e-05	0.00287099	missense	FANCD2	GRCh38.p7	3:10052417	CTGGATAACATATCC[C/T]CTCAGCAAATACGAA	2177
rs774304111	snp	A/C	1.64795e-05	0.00287045	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10081331	CAACTGTCCTAAAAT[A/C]ATTTTTATTTTTAGT	2177
rs774311517	snp	C/G			upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025622	TAATTTGGTAGAATG[C/G]AGATTATCACACTCA	2177
rs774328826	snp	C/G	1.64732e-05	0.0028699	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088471	TGCCAGACAATTCCT[C/G]TGTCGGGTGTGGCCA	2177
rs774354697	in-del	-/ACAAAC/ACAAACAAATGC	3.29545e-05	0.00405911	cds-indel, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087259	TCAGAACAAAGAAAA[-/ACAAAC/ACAAACAAATGC]AATTGGTGATGGGCC	2177
rs774398860	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096867	TCTGTCTTATTCCAG[A/G]AATTACAAATTAATC	2177
rs774404399	snp	A/C	1.71911e-05	0.00293177	intron-variant	FANCD2	GRCh38.p7	3:10060441	CTGTGGTTTAAGATC[A/C]GTTAATCTTGCTAAC	2177
rs774405864	snp	A/G	6.58913e-05	0.00573945	missense	FANCD2	GRCh38.p7	3:10064401	TTCCAGGATGCCTTC[A/G]TAGTGGACTCCTGTG	2177
rs774416811	snp	C/T	3.29478e-05	0.00405867	synonymous-codon	FANCD2	GRCh38.p7	3:10047943	TATGTGTTCATCCAT[C/T]CTGTCGCTGGCTCAG	2177
rs774421197	snp	C/T	1.64735e-05	0.00286993	synonymous-codon	FANCD2	GRCh38.p7	3:10042598	TTGTCGTCTATTAGA[C/T]TGGAGGATTTACCTG	2177
rs774421283	snp	A/G	3.63207e-05	0.00426134	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090398	CAGGTGAGTAAGATA[A/G]TAGTCACTTCAAGAA	2177
rs774452519	in-del	-/TT	1.97108e-05	0.00313927	intron-variant	FANCD2	GRCh38.p7	3:10073002	TATGTTCTTTTCCTC[-/TT]GTCTTGTGTCTCTAA	2177
rs774466311	in-del	-/GTATATACATATATATATGTATATACGTATATGTATATAC			intron-variant	FANCD2	GRCh38.p7	3:10054371	TATATATATATACGT[lengthTooLong]GTATATACATATATA	2177
rs774492211	in-del	-/ACTTTGCCT	1.64738e-05	0.00286995	intron-variant, cds-indel	FANCD2, FANCD2OS	GRCh38.p7	3:10098891	AGTTGGTGGAGCAGA[-/ACTTTGCCT]ACTTATGTTTATTGT	2177
rs774493639	snp	A/G	1.64751e-05	0.00287007	intron-variant	FANCD2	GRCh38.p7	3:10064478	TGGTGAAGTTACATC[A/G]ATTCTGTCAGTAGCT	2177
rs774504069	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088006	CAGCTCATCCTAGTT[A/G]GCAGCACATCAGAAA	2177
rs774509928	snp	C/G/T	3.44734e-05	0.00415159	missense	FANCD2	GRCh38.p7	3:10067274	GCTCACTCGGTTAAA[C/G/T]CACATTGTAGAATTG	2177
rs774580308	snp	C/G	1.66158e-05	0.0028823	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095248	TTGGACACAAGGCTG[C/G]TTCATCACCTGTGTG	2177
rs774592817	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10061232	GCAGTCAGCTCCTCT[A/G]TTGCTGGCTGCCCAG	2177
rs774597445	snp	A/C	1.64732e-05	0.0028699	intron-variant	FANCD2	GRCh38.p7	3:10065385	TAGAAATTTATTTCT[A/C]CTTCTCAGATTGGTG	2177
rs774705850	in-del	-/AGC			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091623	TACCTCATGCCAGTT[-/AGC]AGGAGGCAAACTGGG	2177
rs774707377	snp	C/T	1.65239e-05	0.00287431	stop-gained	FANCD2	GRCh38.p7	3:10064859	GGTCCGGTGACCTCA[C/T]AGGAATCAGGCCAAA	2177
rs774727193	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10079723	AGCCTGGGCCCATGC[C/G]TCAGTGTAGTAGTAA	2177
rs774743051	snp	A/C			missense	FANCD2	GRCh38.p7	3:10028721	ACAGAAGATGCCTCC[A/C]GTAAGTATCTAGTCA	2177
rs774752444	in-del	-/AATAATCTG	3.30989e-05	0.00406797	intron-variant	FANCD2	GRCh38.p7	3:10048099	AACACAGAAAGGGAA[-/AATAATCTG]ATGTTTATTTCTTGT	2177
rs774801047	snp	C/T	4.94637e-05	0.00497287	missense	FANCD2	GRCh38.p7	3:10060355	TCAAGTACAAGCTCA[C/T]TGGGATTATTGGTGC	2177
rs774809459	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094083	TGGTAGGTAAGTCTG[C/T]CTAATTCTGGGGCTT	2177
rs774811607	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10029519	TCAAAAAGGGAGTGG[A/G]GGGCGGGGAGGTTGA	2177
rs774820054	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10033889	TTTTTAGTAGAGACG[C/G]AGTTTCACCGTGTTA	2177
rs774862452	in-del	-/GTTTTGCCATCACG	1.65026e-05	0.00287246	frameshift-variant	FANCD2	GRCh38.p7	3:10043092	GATCTGCAGCATTGT[-/GTTTTGCCATCACG]GTTACAGGCTTCCCA	2177
rs774886640	snp	C/T	1.64738e-05	0.00286995	intron-variant, synonymous-codon	FANCD2, FANCD2OS	GRCh38.p7	3:10098911	GCCTACTTATGTTTA[C/T]TGTCAAATGCTTCTA	2177
rs774919370	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10042490	TTTTCTAATTTTATC[G/T]AACAGTTCAGTACAA	2177
rs774991602	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10072304	TTTTTTTTGAGACAG[A/C]GGCTTGCTTTGTCGC	2177
rs775016476	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10068819	ACCAATGGAACAGAA[A/G]AGAGCCCAGAAATAA	2177
rs775041266	snp	C/T			intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10099487	AAATAAACCTGGGTG[C/T]GGTGGCTCACACCTG	2177
rs775042717	snp	A/G	1.65523e-05	0.00287678	intron-variant	FANCD2	GRCh38.p7	3:10041753	AGAGCCAGCTTTCCA[A/G]CCTCCCAGAACAAGT	2177
rs775049680	snp	C/T	3.55505e-05	0.00421592	intron-variant	FANCD2	GRCh38.p7	3:10039252	CAGAAAGGCTCAGTT[C/T]CCTGTTTTCTCTTCC	2177
rs775049991	in-del	-/CTA	1.66208e-05	0.00288273	cds-indel	FANCD2	GRCh38.p7	3:10049483	CCCATCTGCTATGAT[-/CTA]GATGAATGCTGTCTT	2177
rs775057300	snp	A/T	3.29527e-05	0.00405898	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094356	ACTTCAGTTTTAGAA[A/T]ACACCGGGTAAGAGC	2177
rs775065594	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10031392	CCTGTAGTCCCAGCT[A/G]CTGGGAGGCTGAGGC	2177
rs775067132	snp	A/G	1.64819e-05	0.00287066	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093345	GATTTACTGGGCCCT[A/G]TTTCATATTTATTCT	2177
rs775074145	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096642	TTACTCATGGGCCCT[A/G]GTCACAGGCTGCACC	2177
rs775076333	snp	C/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082218	TTATTCTTTGTCCCT[C/G]CCTCTGCTCTCCACC	2177
rs775086110	snp	A/G	6.59e-05	0.00573983	intron-variant	FANCD2	GRCh38.p7	3:10078231	ATAGGACTTGGGCAT[A/G]GTGGATTTGGGAACA	2177
rs775100997	snp	A/T	3.77117e-05	0.00434217	intron-variant	FANCD2	GRCh38.p7	3:10065998	AGCAGAGTTAATAGG[A/T]TGTTTCACTTATTGT	2177
rs775111979	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10031776	TATTATCTGAAGAAC[A/C]TAAAAAATTCGGATT	2177
rs775157245	snp	C/G	1.67041e-05	0.00288994	intron-variant	FANCD2	GRCh38.p7	3:10039911	TATCACTGCAGTATG[C/G]AAAGAGCAGTAGTAA	2177
rs775163107	snp	C/G	4.94287e-05	0.00497111	missense	FANCD2	GRCh38.p7	3:10041624	TCTACCATTCACAGT[C/G]ACCTACTGATAGAGA	2177
rs775166162	snp	C/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095493	TCAAACTCCAAAGCT[C/G]TTTTTCCTCTAGAAA	2177
rs775167023	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10071564	AACTGGAGGACATTA[C/T]GTTAAGTGAAATAGG	2177
rs775189330	snp	A/G	1.64814e-05	0.00287061	missense	FANCD2	GRCh38.p7	3:10063874	ATGATGAATTTGCCA[A/G]CCTGATCCAACATGA	2177
rs775190657	in-del	-/A			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095000	AACTCTCAGATTGAT[-/A]ACAAGGGACAGAAAT	2177
rs775247764	snp	C/T	1.64743e-05	0.00287	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087144	TACAGCCAGAGCGTC[C/T]ATTACTTGCAGAATT	2177
rs775254530	in-del	-/T			intron-variant	FANCD2	GRCh38.p7	3:10045088	TTGCCTTTTTAACTG[-/T]TTTTTTTTTTTTTCC	2177
rs775257720	snp	A/G	1.64735e-05	0.00286993	synonymous-codon	FANCD2	GRCh38.p7	3:10064738	CCGCAGTGACTTTCC[A/G]TTTCCTGTGAAAGCA	2177
rs775291700	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10080227	AATTCATTCTTCTTT[C/G]TATTCACTATCGGGT	2177
rs775329844	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10069492	CCCCCTCCCCCTCTC[A/C]CGTCTCCCTCTGATG	2177
rs775336123	snp	A/G	3.3006e-05	0.00406226	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085953	ATAGCCAAGATTGTT[A/G]TCCCAAGAAACTCCT	2177
rs775344813	snp	C/G	6.59968e-05	0.00574404	splice-acceptor-variant	FANCD2	GRCh38.p7	3:10036286	ATGTCTTCTTTTTTA[C/G]CCTGCCATTATCAAA	2177
rs775357192	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10062752	TCTCAACTCTGTCGC[C/G]AAGGCTGGAGTGCGG	2177
rs775410345	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10060872	TCGGTTTGGGGGCTT[A/G]ATAAGATGTTGCCAT	2177
rs775426090	snp	A/G	1.64838e-05	0.00287083	missense	FANCD2	GRCh38.p7	3:10046592	TAGGTGTTTGACCTG[A/G]TGATGCTTTTCATCA	2177
rs775474773	in-del	-/T	1.65074e-05	0.00287288	intron-variant	FANCD2	GRCh38.p7	3:10034543	ATCCCAAAGTATGTA[-/T]TTTTTCCCCTGGTAT	2177
rs775507510	snp	A/G	0.00010012	0.00707461	intron-variant	FANCD2	GRCh38.p7	3:10032812	ATTTGCCATATTCTT[A/G]AAAATTTTTCTATTT	2177
rs775517107	in-del	-/T	1.64749e-05	0.00287005	frameshift-variant, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092202	GAAGAGAAACTCCTC[-/T]ACTGGAACATGGCTG	2177
rs775519124	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094229	ATGAGACTATTCTGC[C/T]TCAGGGGCCTTTCAG	2177
rs775538190	snp	A/G	3.29478e-05	0.00405867	synonymous-codon	FANCD2	GRCh38.p7	3:10047946	GTGTTCATCCATTCT[A/G]TCGCTGGCTCAGAGT	2177
rs775540976	snp	A/C	1.6476e-05	0.00287014	missense	FANCD2	GRCh38.p7	3:10035193	GTGCATCTTATTCTA[A/C]GAGTCTCATCAAACT	2177
rs775558611	snp	A/G	1.6804e-05	0.00289858	intron-variant	FANCD2	GRCh38.p7	3:10072829	GTCTAATGGTGGTGT[A/G]TAATTGGTACACATT	2177
rs775561668	snp	C/T	1.64732e-05	0.0028699	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085829	GTGGATTTTCTCAAC[C/T]TGAAAATCAGAATTT	2177
rs775602382	snp	C/T			upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025807	TCAATACGTCCTAGA[C/T]CCTGTGCTAAGGGAT	2177
rs775624233	snp	G/T	3.53245e-05	0.0042025	intron-variant	FANCD2	GRCh38.p7	3:10052521	CAATATGTTGGGAAA[G/T]ATTTTTTTTTTTTTG	2177
rs775624276	snp	A/G	1.71888e-05	0.00293157	intron-variant	FANCD2	GRCh38.p7	3:10046530	TTCATTGTAGCAAAT[A/G]TACTGATTTGTTAAC	2177
rs775627965	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100348	AGAACAGAATTTTGT[A/G]CTGGATTCCTGTTGA	2177
rs775736013	snp	A/G	1.64735e-05	0.00286993	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088477	ACAATTCCTCTGTCG[A/G]GTGTGGCCAAGTGGG	2177
rs775776546	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10037045	AGGTGGGGTTTCGCC[A/G]TGTTGCCCAGGCTAG	2177
rs775783935	in-del	-/CCTCTCCC			intron-variant	FANCD2	GRCh38.p7	3:10069460	ACCCTAGTTAAGATG[-/CCTCTCCC]CCTCCCCCTCCCCCT	2177
rs775806507	snp	C/T	3.30109e-05	0.00406256	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096513	AATCCCCTACTCTTA[C/T]TCTTTGTGACAGCAT	2177
rs775820263	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10066332	TAGAATGTATTTGTG[C/T]TTGGTGATAATGACA	2177
rs775831214	snp	A/G	1.65979e-05	0.00288074	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090319	TGTTTTCTTCCGTGT[A/G]ATGATGGCTGAACTA	2177
rs775862865	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10049280	GATTGTGATTTTAAC[A/G]AAGTAGAGATTGGAG	2177
rs775898191	snp	C/T	1.64898e-05	0.00287135	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096339	AGATTCACCAGGACA[C/T]GAGACTCACCCAACA	2177
rs775918808	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10035530	CTTTATCATATTCAT[A/G]TCTACATTATCTCCC	2177
rs775919604	snp	C/G	1.67472e-05	0.00289367	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101140	TATTCCAGAGGTCAC[C/G]CAGAGCAGTAACCTA	2177
rs775920266	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10079507	GATGGGGTTTTAACA[C/T]GTTCATCAGGCTGAT	2177
rs775921172	in-del	-/A	0.201664	0.245283	intron-variant	FANCD2	GRCh38.p7	3:10062127	GTATAATAATAATTT[-/A]AAAAAAAAATTCTTT	2177
rs775929601	snp	A/G	1.68374e-05	0.00290145	intron-variant	FANCD2	GRCh38.p7	3:10043779	AATAAGGTGTAACGT[A/G]TTTCGCTGATGTGTC	2177
rs775932167	snp	C/T	3.96079e-05	0.00444999	intron-variant	FANCD2	GRCh38.p7	3:10046774	CAGAAAGCTTTACAG[C/T]TCTCATGTAAAATTT	2177
rs775934513	snp	C/G			splice-donor-variant, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094364	TTTAGAAAACACCGG[C/G]TAAGAGCTAAGAGCA	2177
rs775943873	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10080823	TTTGTCAACCTAAAT[A/G]ATTTCTACTTTTATG	2177
rs776008992	in-del	-/TTT			intron-variant	FANCD2	GRCh38.p7	3:10030097	TGGCCCATTATATCA[-/TTT]TTTTTTTTTTTTTTG	2177
rs776010397	snp	G/T	1.68969e-05	0.00290657	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095187	AGAGCATTTATAAAC[G/T]TATTGGTTATAGGAA	2177
rs776012437	snp	G/T	1.65446e-05	0.00287612	missense	FANCD2	GRCh38.p7	3:10043539	ATTCTCCTCTTTGAT[G/T]TAATAAAGTCAGCTA	2177
rs776029741	snp	C/T	0.000113218	0.00752305	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090437	TGGATTACTTGGAAG[C/T]TGCTGATTTTTTTTT	2177
rs776042877	snp	A/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081983	CTGTTCTCATTATAC[A/T]AGATTTCTGGTCAAT	2177
rs776116877	snp	A/G	0.000131778	0.00811614	synonymous-codon	FANCD2	GRCh38.p7	3:10065400	CCTTCTCAGATTGGT[A/G]TCTCCGCTGTGCCTG	2177
rs776126413	snp	C/T			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027578	CCTTCTACTGGCTAA[C/T]TGCTGTTTCAGCCCT	2177
rs776128305	snp	A/C	3.4205e-05	0.00413537	intron-variant	FANCD2	GRCh38.p7	3:10062100	GTTGTGCACATGTAC[A/C]CTAAAACTTAAAGTA	2177
rs776158545	in-del	-/T			intron-variant	FANCD2	GRCh38.p7	3:10030099	GCCCATTATATCATT[-/T]TTTTTTTTTTTTTTG	2177
rs776200840	snp	C/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10080963	CCCTCTGTCAGAATA[C/G]AGTCTTAGGTTAACA	2177
rs776202513	in-del	-/C	1.64732e-05	0.0028699	intron-variant	FANCD2	GRCh38.p7	3:10049527	TATTGGCTTCTTGTA[-/C]TTTAGATATTGAATA	2177
rs776209053	snp	A/G	0.000135437	0.00822801	intron-variant	FANCD2	GRCh38.p7	3:10043008	CTGTGCCTACCCACT[A/G]TGAATGAGCAGAAAA	2177
rs776210193	snp	A/C	3.29478e-05	0.00405867	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087167	GCAGAATTTCCATCA[A/C]AGCATTCCCAGTTTC	2177
rs776221333	snp	C/T	2.08396e-05	0.00322791	intron-variant	FANCD2	GRCh38.p7	3:10066017	TTCACTTATTGTGCA[C/T]AGTTTTTCTCAAAAC	2177
rs776229184	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10067440	AATCTCAGGCCAATA[G/T]CCCTGATGAACATTG	2177
rs776231185	snp	C/T	1.68207e-05	0.00290001	intron-variant	FANCD2	GRCh38.p7	3:10049330	CTTTAGAATGGCCAT[C/T]CATATTTTGTTTTAC	2177
rs776237043	snp	A/G	1.65048e-05	0.00287265	intron-variant	FANCD2	GRCh38.p7	3:10063942	TTTTCTTAAAGCAAT[A/G]AAGCATGAGAGCTGC	2177
rs776292242	in-del	-/CTGT			intron-variant	FANCD2	GRCh38.p7	3:10062243	CTTTCTTTCTTTTTC[-/CTGT]CTTTTTTTTTTTTTT	2177
rs776304865	snp	A/G	1.64923e-05	0.00287156	missense, downstream-variant-500B	FANCD2, FANCD2OS	GRCh38.p7	3:10081122	GAAGCCGGAATATTG[A/G]ATTCTCACATCTCCA	2177
rs776311610	snp	C/T	1.64765e-05	0.00287019	missense	FANCD2	GRCh38.p7	3:10074639	ATTGTGGACTTGTGA[C/T]GAAGTTCATCTTAGA	2177
rs776315102	snp	C/T			intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10099210	GAAATGTGAAAGCAT[C/T]TGGTGAAAGCCAAAG	2177
rs776326873	snp	A/C	1.64727e-05	0.00286986	missense	FANCD2	GRCh38.p7	3:10049413	CATATCTGCAGTGGG[A/C]ATGAAGCTGAAGTTG	2177
rs776396195	snp	A/C	3.30235e-05	0.00406333	synonymous-codon	FANCD2	GRCh38.p7	3:10060315	ATGCACTTGGTGATA[A/C]GAAAGCAGCTCTCTA	2177
rs776438516	snp	A/C			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085050	TAATCCAAAGATAGA[A/C]ATGTCAAGACTTGAC	2177
rs776482951	snp	A/G	4.94401e-05	0.00497168	missense	FANCD2	GRCh38.p7	3:10046679	ATTCGATCAGGCTGC[A/G]TTCAAGAACAGCTGC	2177
rs776507961	snp	G/T	0.000445099	0.0149114	missense	FANCD2	GRCh38.p7	3:10067244	GGAAACATCACCTGA[G/T]ATGAAGGGGAAGGTG	2177
rs776562018	snp	A/G	1.64827e-05	0.00287073	intron-variant	FANCD2	GRCh38.p7	3:10042510	GTTCAGTACAAAGTT[A/G]AGGTAGTGACATGAA	2177
rs776582980	in-del	-/T			intron-variant	FANCD2	GRCh38.p7	3:10058668	CACATATATGAAGGC[-/T]TATCTTTGAACTCTG	2177
rs776594391	snp	C/T	3.29522e-05	0.00405894	synonymous-codon	FANCD2	GRCh38.p7	3:10046618	CATCATCTATAGCAC[C/T]AATACTCAGACAAAG	2177
rs776611755	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10074381	GTCTTGGGAATATTT[A/G]GGGACTTGGGCTAGA	2177
rs776697934	snp	A/G	1.64732e-05	0.0028699	intron-variant	FANCD2	GRCh38.p7	3:10064699	GCGTATTCCTGAGCT[A/G]CAACATCAGATTCTG	2177
rs776717633	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10079450	GCTGGGGACTACAGG[C/T]GCGCGCCACCACACC	2177
rs776720139	snp	C/T			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027370	CTGAGTAGGAATTTC[C/T]AGGCAAATAAGAGCA	2177
rs776742448	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10046281	GATGGTCTCGATCTC[C/G]TGACCTTGTGATCTG	2177
rs776756572	snp	A/G	1.67377e-05	0.00289284	intron-variant	FANCD2	GRCh38.p7	3:10036387	CCCTGATGTACTTAA[A/G]TTCTCTCTGAAAAGG	2177
rs776789253	snp	A/G	7.13318e-05	0.00597167	intron-variant	FANCD2	GRCh38.p7	3:10052541	TTTTTTTTTTGAGAC[A/G]GAGTCTAGCTCTGTC	2177
rs776858997	in-del	-/C	5.13228e-05	0.00506545	intron-variant	FANCD2	GRCh38.p7	3:10034668	ACTAAAAATTTTATT[-/C]TTTTTTATTTTTTAA	2177
rs776902141	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10059883	TGACTTGCTAAAGAC[A/G]CACAGGGCTGGGTAT	2177
rs776906387	snp	C/T	1.64741e-05	0.00286998	synonymous-codon	FANCD2	GRCh38.p7	3:10064759	TGTGAAAGCACTGTA[C/T]GGACTGGAAGAATAC	2177
rs776943888	snp	A/G	1.65269e-05	0.00287457	intron-variant	FANCD2	GRCh38.p7	3:10028758	GCTTTATTTCCTGTA[A/G]CAATGTGTGAGGCAT	2177
rs776959147	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098444	TCGACTTAGAGTCAC[C/T]AATACAGTCTAGCCT	2177
rs776972450	snp	A/T	1.64855e-05	0.00287097	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085933	CTCAGGTGAGTCATA[A/T]CTACATAGCCAAGAT	2177
rs776993494	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10046167	CACGCCATTCTCCTG[C/G]CTCAGCCTCCCCAGC	2177
rs776996293	snp	A/G			downstream-variant-500B, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10102269	CTGTCTCAGCCCCCT[A/G]TATAGGTGGGACTAC	2177
rs777012622	in-del	-/C			intron-variant	FANCD2	GRCh38.p7	3:10069011	ATTATAGACTTAAAT[-/C]TAAGACTTCAAATTA	2177
rs777012727	snp	C/G	4.22958e-05	0.00459849	intron-variant	FANCD2	GRCh38.p7	3:10073015	TCTTGTCTTGTGTCT[C/G]TAAATAAGCTTCATT	2177
rs777030917	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10056341	GGTGTATATCTAAGA[C/G]TGGAATTGCTGGATC	2177
rs777042522	snp	C/T	3.29478e-05	0.00405867	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088796	ATTCTACTTTGTTAA[C/T]TAGTGGGTCAAATAT	2177
rs777055464	snp	A/G	3.38822e-05	0.00411582	intron-variant	FANCD2	GRCh38.p7	3:10043005	GGACTGTGCCTACCC[A/G]CTATGAATGAGCAGA	2177
rs777057249	snp	A/C	1.6486e-05	0.00287102	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092250	CTCATCAACTTGATA[A/C]AGGTGAGTATGGAGA	2177
rs777064024	snp	A/G	3.31186e-05	0.00406918	intron-variant	FANCD2	GRCh38.p7	3:10039883	TCTAAGTGAGGCTCA[A/G]CTATGGGGGTTCTAT	2177
rs777070767	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10057445	TCTCAGCTCACTCCA[A/G]CCTCCGCCTCCCAGG	2177
rs777089905	snp	C/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097911	CGTTCTTCTGTCAAG[C/G]CTTCAGCCGGTCCCT	2177
rs777119070	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10044956	GTCTGCATTGTCTTC[A/G]TTGTTATCTTTAATG	2177
rs777142423	snp	C/T	3.29495e-05	0.00405877	missense	FANCD2	GRCh38.p7	3:10048010	TTTGGCAGTCTCCTA[C/T]ACAAATATGCATTTA	2177
rs777184746	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10039637	TTTATTTCTCAAATA[A/G]TTTCAGCTCTGCATT	2177
rs777197502	in-del	-/T	1.68493e-05	0.00290248	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088578	AATGAGCCAAATAGC[-/T]TTTTTTCTATTTTGC	2177
rs777237116	snp	A/G	1.65809e-05	0.00287926	missense	FANCD2	GRCh38.p7	3:10032840	TTTTCAGAAACCAGG[A/G]AGCAACCACTTTCCA	2177
rs777250911	snp	C/T	1.75369e-05	0.00296111	intron-variant	FANCD2	GRCh38.p7	3:10062237	TTTTTCCTTTCTTTC[C/T]TTTTCCTGTCTTTTT	2177
rs777254344	snp	A/G	1.64741e-05	0.00286998	intron-variant	FANCD2	GRCh38.p7	3:10064455	TTTACCTGCTGGCTT[A/G]GTTGCACTGGTGAAG	2177
rs777276871	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10064701	GTATTCCTGAGCTGC[A/C]ACATCAGATTCTGGT	2177
rs777306543	snp	A/G			synonymous-codon	FANCD2	GRCh38.p7	3:10043547	CTTTGATGTAATAAA[A/G]TCAGCTATTAGATAT	2177
rs777336575	snp	C/T	1.64798e-05	0.00287047	intron-variant	FANCD2	GRCh38.p7	3:10063774	CAAGGTTTAAACCAT[C/T]CTTCCTCTTTGCTCC	2177
rs777339430	snp	C/T	1.64887e-05	0.00287125	missense	FANCD2	GRCh38.p7	3:10052493	AAGCCAGCAGCCACA[C/T]CCAGGTAAGAGGCAA	2177
rs777340649	snp	C/G/T	4.9473e-05	0.00497337	missense	FANCD2	GRCh38.p7	3:10052405	ATTTTAGATTATCTG[C/G/T]ATAACATATCCCCTC	2177
rs777378549	snp	C/T	1.64727e-05	0.00286986	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088843	TATCTACCTGGAGCA[C/T]ACAGAGAGCATTCTG	2177
rs777414689	in-del	-/GAT			intron-variant	FANCD2	GRCh38.p7	3:10071945	TGTACTTTTGGTGCA[-/GAT]GATGGGGTTTCACCG	2177
rs777481151	in-del	-/T/TT			intron-variant	FANCD2	GRCh38.p7	3:10076284	TCCCTTGAATTAGTC[-/T/TT]TTTTTTTTTTTTCCC	2177
rs777481323	in-del	-/C			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081724	ATGTGGCCATCTGTT[-/C]CTTAGTCCAGTTTCC	2177
rs777481665	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10074992	GGTTCTTAGAAGTCA[A/G]TGCCCTTTTCACTTT	2177
rs777509355	snp	A/G	3.29652e-05	0.00405974	missense	FANCD2	GRCh38.p7	3:10028700	TCTGAGGATAAAGAG[A/G]GCCTGACAGAAGATG	2177
rs777510450	snp	C/T	1.72389e-05	0.00293584	intron-variant	FANCD2	GRCh38.p7	3:10035156	AAGTGGAAAACAGAT[C/T]TCTTTTTTTTTTACA	2177
rs777514146	in-del	-/GACT	1.64749e-05	0.00287005	frameshift-variant, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085877	ATGTCCTTAGTAGCC[-/GACT]GAAACAGGGAGAACA	2177
rs777533071	snp	G/T	1.71799e-05	0.00293081	intron-variant	FANCD2	GRCh38.p7	3:10073236	CTTGAGTCACTTTTC[G/T]CTTTTTAATATAAAA	2177
rs777539464	snp	A/G	4.94205e-05	0.0049707	missense	FANCD2	GRCh38.p7	3:10047981	TTCACTCTCTAGACC[A/G]GAGTATAATTTCATT	2177
rs777558355	in-del	-/TTGG			intron-variant	FANCD2	GRCh38.p7	3:10044652	TTTAAAGATTTTTCT[-/TTGG]TTGGAATCTGTTTTG	2177
rs777577310	snp	C/G	6.58913e-05	0.00573945	intron-variant	FANCD2	GRCh38.p7	3:10064706	CCTGAGCTGCAACAT[C/G]AGATTCTGGTTTTTC	2177
rs777594776	in-del	-/A	1.64811e-05	0.00287059	frameshift-variant	FANCD2	GRCh38.p7	3:10039844	GTGGGGAAAGAACTC[-/A]GGTGGATAAACCCTC	2177
rs777598119	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10066060	TCCCACAAGACTCCC[C/T]AGAAGTCTTCACCAA	2177
rs777620616	snp	C/T	8.23662e-05	0.00641688	intron-variant	FANCD2	GRCh38.p7	3:10042672	ACTTGAGGTATGCTC[C/T]TATATCCCATCACAC	2177
rs777639581	snp	G/T	3.29468e-05	0.00405861	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085783	TTTTCCAGAAACTAA[G/T]CTAACCCCTCTTACC	2177
rs777644713	snp	A/G	1.64741e-05	0.00286998	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092194	AGATTCATGAAGAGA[A/G]ACTCCTCTACTGGAA	2177
rs777646197	snp	G/T	1.67908e-05	0.00289743	missense	FANCD2	GRCh38.p7	3:10062158	GTTTTTAGAAGTGAA[G/T]CACCTAGTTTGACCC	2177
rs777719596	in-del	-/GT	1.64851e-05	0.00287093	splice-donor-variant	FANCD2	GRCh38.p7	3:10028722	CAGAAGATGCCTCCA[-/GT]AAGTATCTAGTCATT	2177
rs777727311	snp	C/G	1.65151e-05	0.00287355	missense	FANCD2	GRCh38.p7	3:10072930	ACTTTAGATATAACA[C/G]CTCATACTGTTACTG	2177
rs777729489	snp	A/C	1.64727e-05	0.00286986	missense, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10081416	AGTACCACATAATGT[A/C]TTCCTGCTATCAGAG	2177
rs777785160	snp	A/G			synonymous-codon	FANCD2	GRCh38.p7	3:10073269	AAGGAAACAAAAAAC[A/G]GATGGCAGCAAGACA	2177
rs777787616	snp	A/G			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026995	CCGAGTTAGAATCCC[A/G]GTTCTGCCCGTGATG	2177
rs777790646	snp	A/G	1.64773e-05	0.00287026	missense	FANCD2	GRCh38.p7	3:10039832	CAGCACGCTGATGTG[A/G]GGAAAGAACTCAGGT	2177
rs777792026	snp	A/G	0.000780234	0.019736	intron-variant	FANCD2	GRCh38.p7	3:10032382	ACCTCCTGGGCTCAA[A/G]TTATTCTTCCGCCTT	2177
rs777797004	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10057186	AATTAGGTTTTTGTC[A/G]TTTTGAGGTATGGGA	2177
rs777812740	snp	C/T	1.64787e-05	0.00287038	synonymous-codon	FANCD2	GRCh38.p7	3:10047919	TTCCCCACTCAAGGT[C/T]CTTAAGGATATGTGT	2177
rs777842000	snp	A/G	1.64727e-05	0.00286986	synonymous-codon	FANCD2	GRCh38.p7	3:10065433	TCCGTATTTCCGGTT[A/G]CTGAGACTTTGTGTG	2177
rs777842078	snp	C/T	3.39576e-05	0.00412039	intron-variant	FANCD2	GRCh38.p7	3:10060427	GGAGATTCTGACTTC[C/T]GTGGTTTAAGATCAG	2177
rs777872939	in-del	-/AT			intron-variant	FANCD2	GRCh38.p7	3:10054379	TATACGTGTATATAC[-/AT]ATATATATGTATATA	2177
rs777904095	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10041340	CTTTTTCCTTTTTGC[A/G]GGGAAGGATACATAC	2177
rs777920890	snp	C/T	1.654e-05	0.00287571	intron-variant	FANCD2	GRCh38.p7	3:10074722	TTCTTTCAGAAAGTT[C/T]CTCAGGTCTATTCTT	2177
rs777979536	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10075643	AGAGAGTAGAATTTC[C/T]CTAGGTTTAAGAGAA	2177
rs777999452	snp	C/G/T	3.3241e-05	0.00407671	missense	FANCD2	GRCh38.p7	3:10049481	AAACCCATCTGCTAT[C/G/T]ATGATGAATGCTGTC	2177
rs778004562	snp	A/G	8.23608e-05	0.00641667	synonymous-codon	FANCD2	GRCh38.p7	3:10049391	AGTGGTTGGTGCCTT[A/G]GTGACCCATATCTGC	2177
rs778023061	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10040422	TGGCCAGTGGAGAAG[C/T]TGACCATGATCCCTT	2177
rs778024004	snp	G/T	1.64792e-05	0.00287042	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101226	TGCTGGAGAAAAGGA[G/T]CAAGATAGTGATGAG	2177
rs778028392	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093724	TTCTCTTTTGTGGGA[A/G]TAGCCTGTATTAGCC	2177
rs778030235	snp	C/G	1.64787e-05	0.00287038	missense	FANCD2	GRCh38.p7	3:10074593	CATGCTTTTTTCCGA[C/G]AGCTGGACATTGAGG	2177
rs778033375	snp	C/T	1.64768e-05	0.00287021	intron-variant	FANCD2	GRCh38.p7	3:10065370	CTATGAAGTGTGGTC[C/T]AGAAATTTATTTCTC	2177
rs778052246	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10044109	AGGGGAAATACTAAC[A/C]GTGTAAACAAGCACA	2177
rs778065365	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10035593	TTTGTCCTTTTCCTC[C/T]TCCTCGTCTCTTTTA	2177
rs778078792	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10072525	CTCAGGTGATCCGCG[C/T]GCCTTGACCTCCCAA	2177
rs778092384	snp	C/T	1.65075e-05	0.00287289	intron-variant	FANCD2	GRCh38.p7	3:10034542	CTATCCCAAAGTATG[C/T]ATTTTTCCCCTGGTA	2177
rs778126667	in-del	-/AC	6.60622e-05	0.00574689	intron-variant	FANCD2	GRCh38.p7	3:10048085	TTTGGCAAGGAGGGA[-/AC]ACAGAAAGGGAAAAT	2177
rs778178069	snp	A/G	5.02694e-05	0.0050132	intron-variant	FANCD2	GRCh38.p7	3:10043624	TTTGATTATCAAGGA[A/G]GAAATGAGTGGCAAT	2177
rs778178918	snp	C/T	1.64754e-05	0.00287009	intron-variant	FANCD2	GRCh38.p7	3:10042541	AACCTATTAAGTTTC[C/T]GTGCTTTTAATTTTT	2177
rs778203905	snp	G/T	1.65081e-05	0.00287293	intron-variant	FANCD2	GRCh38.p7	3:10064337	TGCACTGCCCTTTTT[G/T]TTTGTTTGCTTCCTG	2177
rs778207357	snp	C/T	1.64743e-05	0.00287	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087131	TTTCTTGTCTCCTTA[C/T]AGCCAGAGCGTCCAT	2177
rs778219361	snp	A/C	0.00013136	0.00810327	missense	FANCD2	GRCh38.p7	3:10067209	ATTTGTACTTTGCAG[A/C]TTGTAAATGCCTTCT	2177
rs778286669	snp	A/G	3.30693e-05	0.00406615	intron-variant	FANCD2	GRCh38.p7	3:10034432	AAGGAAAACTATGGT[A/G]GGAAACTGGTGACCA	2177
rs778289599	snp	A/T	1.64803e-05	0.00287052	missense	FANCD2	GRCh38.p7	3:10041709	CAAACTTCCTATTGA[A/T]GGTAGAAAAGACTCA	2177
rs778292547	snp	A/G	1.6473e-05	0.00286988	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094326	CATTTCTGAAGCAAT[A/G]TATGCCGCTCCTAGA	2177
rs778303459	snp	C/T	8.23608e-05	0.00641667	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088863	AGAGCATTCTGAAGG[C/T]CATAGAGGAGATTGC	2177
rs778319075	in-del	-/T			intron-variant	FANCD2	GRCh38.p7	3:10062888	CGGGGTTTCACCATG[-/T]TGGGGTTTCGCTATG	2177
rs778324363	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10072420	AGTAGCTGGGATTAC[A/C]GGCGTCTGCCAGCAC	2177
rs778340315	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10064161	ATCTGTCTGAGAGCC[C/G]TATTCTGTGCTGGGC	2177
rs778403934	snp	A/C			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087041	TTAGGCCGTCAAACA[A/C]TGAAAGGGACTTGGG	2177
rs778424847	snp	C/T			intron-variant, missense	FANCD2, FANCD2OS	GRCh38.p7	3:10098897	TGGAGCAGAACTTTG[C/T]CTACTTATGTTTATT	2177
rs778447238	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10067353	TGGTAGTACTACTAG[G/T]CCAGTAGTGAGGCAA	2177
rs778488560	snp	A/C	1.64942e-05	0.00287173	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094410	CACTGAAGAGTTGCT[A/C]AGAAGATATGTCCTT	2177
rs778504315	snp	A/G	1.87243e-05	0.00305971	intron-variant	FANCD2	GRCh38.p7	3:10065995	GTGAGCAGAGTTAAT[A/G]GGATGTTTCACTTAT	2177
rs778517804	snp	A/G	1.64841e-05	0.00287085	missense, downstream-variant-500B	FANCD2, FANCD2OS	GRCh38.p7	3:10081190	CAACTGCTGACCCCA[A/G]TGTGTAACCACCTGG	2177
rs778520844	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10066766	GTCTTGCTCTGTCAC[C/T]CAGGCTGGAGTGCGG	2177
rs778607658	snp	C/T	1.65282e-05	0.00287469	synonymous-codon, downstream-variant-500B	FANCD2, FANCD2OS	GRCh38.p7	3:10081102	GCATTTATTATAGAA[C/T]AAAGGAAGCCGGAAT	2177
rs778650034	in-del	-/TTCTAC	1.64743e-05	0.00287	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088810	TTAGTGGGTCAAATA[-/TTCTAC]TTTGACTCTCAATGC	2177
rs778661237	snp	C/T	6.10147e-05	0.00552301	intron-variant	FANCD2	GRCh38.p7	3:10066013	ATGTTTCACTTATTG[C/T]GCATAGTTTTTCTCA	2177
rs778662654	snp	A/C/T	5.10611e-05	0.00505256	intron-variant	FANCD2	GRCh38.p7	3:10043189	GATGTCACAATTTTC[A/C/T]GACATCCCACTGTCA	2177
rs778668454	snp	C/T	1.64757e-05	0.00287012	missense	FANCD2	GRCh38.p7	3:10064806	TTGCCATAAACCTCC[C/T]GCCGCTGCTGTTTTC	2177
rs778677652	snp	C/G	1.65493e-05	0.00287652	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098738	GAAGAGATTAAGTCC[C/G]AAAATTCCCAGGAGA	2177
rs778684735	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10074163	CTTGGCCAGGCAGGT[C/G]TCAAACTCCTGACCT	2177
rs778691779	snp	A/G	3.3083e-05	0.00406699	missense	FANCD2	GRCh38.p7	3:10072939	ATAACACCTCATACT[A/G]TTACTGCTATTTCAG	2177
rs778698499	snp	C/T	1.68707e-05	0.00290432	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090258	CTAAGCAGTGCATCA[C/T]GGTGTGGGCACGCAT	2177
rs778701257	snp	C/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090192	GTGAAAGGACATTTA[C/G]AGAGGTAGGGAAGGA	2177
rs778717257	snp	C/T					GRCh38.p7	3:10077580	TTTTTTTTTCACCCA[C/T]TGGGAAGTATTAACA	2177
rs778724614	in-del	-/TG	3.39674e-05	0.00412099			GRCh38.p7	3:10046546	TACTGATTTGTTAAC[-/TG]TTTTTCTGTTGTTGC	2177
rs778754133	snp	A/G	1.67024e-05	0.0028898			GRCh38.p7	3:10060287	TTTCTTCATCATCTC[A/G]TTGCAGGATGACATG	2177
rs778758088	snp	A/G	1.64879e-05	0.00287118			GRCh38.p7	3:10036273	CTCCTAACTCCCTAT[A/G]TCTTCTTTTTTAGCC	2177
rs778794561	snp	A/G	1.64762e-05	0.00287016	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085897	AAACAGGGAGAACAC[A/G]GCCAGCCTTTGGAGG	2177
rs778797472	snp	C/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092526	TCACTTTTTCACCTT[C/G]CCTTGGATCCTCTAT	2177
rs778798671	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10040320	GGATTACAGGCATGA[A/G]CCACCGTGCCTGGCC	2177
rs778829115	in-del	-/G			intron-variant	FANCD2	GRCh38.p7	3:10032526	GCCCAGGCTGGTCTT[-/G]GAACTCCTGGCTTCA	2177
rs778865461	snp	C/T	6.60175e-05	0.00574494	missense	FANCD2	GRCh38.p7	3:10043104	TGTGTTTTGCCATCA[C/T]GGTTACAGGCTTCCC	2177
rs778891531	in-del	-/ATCTC			intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10099638	TGGCACGTGCCTGTT[-/ATCTC]AGCTACTTGGGAGGC	2177
rs778899016	in-del	-/A	1.6501e-05	0.00287232	intron-variant	FANCD2	GRCh38.p7	3:10041594	TTCAAACCATTATAC[-/A]AACTTTTTTCTTTTT	2177
rs778966201	snp	A/G	1.64882e-05	0.00287121	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096493	CCTTGGATCCTGCTA[A/G]TGATAATCCCCTACT	2177
rs778969666	snp	C/G	1.64789e-05	0.0028704	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101241	GCAAGATAGTGATGA[C/G]AGTTATGATGACTCT	2177
rs778974182	snp	A/T	4.94205e-05	0.0049707	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085796	AAGCTAACCCCTCTT[A/T]CCTTGACTTCCTTAG	2177
rs778990634	in-del	-/C	1.64811e-05	0.00287059	frameshift-variant	FANCD2	GRCh38.p7	3:10063907	AGCTGGATCCAAAAG[-/C]CCTGGTAAAGCCAAT	2177
rs779004915	in-del	-/A			intron-variant	FANCD2	GRCh38.p7	3:10071507	GTACTATTCAGCCAT[-/A]AAAAAACAATGAGAT	2177
rs779037209	in-del	-/AGG			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091770	AACAAAAAACAGCTT[-/AGG]AGAAAACTTGGACCC	2177
rs779042452	snp	A/G			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026948	CAAGAGTAAGTATAG[A/G]TGGTGAAGAGCGCAG	2177
rs779060030	snp	A/G	1.67217e-05	0.00289147	missense	FANCD2	GRCh38.p7	3:10065864	TTTGTTCTCTCTCAG[A/G]TTGTCCTATATTCCT	2177
rs779064246	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10055941	TTGAGTGCAATGGCA[C/T]AATCTTGGCTTACCG	2177
rs779065139	snp	C/T			utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101844	TCTGAGTCATGATTC[C/T]GGACTTTGGGAGCTA	2177
rs779084627	snp	G/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095089	TGATTATCAGCATAG[G/T]CTGGAAACTGCAGAG	2177
rs779116559	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10072054	CATGAGCCAGAGAGC[C/T]CAGCCAAGATCTAGT	2177
rs779155076	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10032124	TGCTGGGATTACAGG[C/T]GTGAGCCACTGTGCT	2177
rs779166407	snp	C/G	3.29522e-05	0.00405894	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092217	TACTGGAACATGGCT[C/G]TTCGAGACTTCAGTA	2177
rs779216164	snp	A/G	3.295e-05	0.00405881	missense	FANCD2	GRCh38.p7	3:10039736	GACCTCACCACCAAG[A/G]TCATGCAGCTGATCA	2177
rs779242727	snp	A/G/T	3.47943e-05	0.00417087	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090379	CACAGCAGCAGACTC[A/G/T]CAGCAGGTGAGTAAG	2177
rs779245007	snp	A/G	1.64738e-05	0.00286995	missense	FANCD2	GRCh38.p7	3:10078158	GAAGCTGGAGAGTAT[A/G]CTGACACCTCCTATT	2177
rs779249492	snp	A/C	1.65891e-05	0.00287998	synonymous-codon	FANCD2	GRCh38.p7	3:10062172	ATCACCTAGTTTGAC[A/C]CAAGAGAGAGCCAAC	2177
rs779309780	snp	C/T	3.96283e-05	0.00445113	intron-variant	FANCD2	GRCh38.p7	3:10034831	GGAATCTTGCTGAAA[C/T]TCAGTCTGTTTTGCC	2177
rs779350241	snp	A/C	1.64849e-05	0.00287092	intron-variant	FANCD2	GRCh38.p7	3:10064350	TTGTTTGTTTGCTTC[A/C]TGAAGGAATGGGTTG	2177
rs779366532	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082700	CTCTTGAGATCTGAA[C/T]TTAAGCATCCATCCT	2177
rs779371801	snp	G/T			splice-acceptor-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10081345	TCATTTTTATTTTTA[G/T]TGTTTAGCTGCTGAG	2177
rs779387854	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10042942	ATGTCCAACATTTAA[A/G]TTTTTTTCTTCCTCA	2177
rs779406688	snp	A/C	4.62396e-05	0.00480808	intron-variant	FANCD2	GRCh38.p7	3:10034645	TGATTTTTAACAGCA[A/C]ATATTAAACTAAAAA	2177
rs779440211	snp	C/T	1.64806e-05	0.00287054	intron-variant	FANCD2	GRCh38.p7	3:10078032	GAAAAAAAATTATCA[C/T]GAAATGACTAGGACA	2177
rs779453561	snp	A/C	1.6492e-05	0.00287154	missense, downstream-variant-500B	FANCD2, FANCD2OS	GRCh38.p7	3:10081227	TTCACAACTATTTTC[A/C]GGTCAGAAGCCTAGA	2177
rs779491341	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10045444	AAGTGCTGGGATTAT[A/G]GGCGTGAGCCACCAT	2177
rs779496643	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10061936	GAGAACACATGGACA[C/T]AGGAAAGGGAACATC	2177
rs779538475	snp	C/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096136	TTGGTGGTATGTCTT[C/G]TAGGCTTTGAATTCT	2177
rs779549178	snp	C/T	1.64727e-05	0.00286986	synonymous-codon, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10081378	TCACGGTGTAGTTGA[C/T]GGACCAGGAGTGAAA	2177
rs779552164	snp	C/T	1.96524e-05	0.00313461	splice-donor-variant	FANCD2	GRCh38.p7	3:10067319	AAAGTACTTGGCAGG[C/T]AAGAGAAGTGTCCTA	2177
rs779586699	snp	C/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086066	TCATATATGAGCTTT[C/G]TCATCTATGTATTCT	2177
rs779615596	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10047428	AAGCTATGTTTATTA[A/G]CTGGTTATTTAGTCT	2177
rs779632231	snp	A/G	1.64776e-05	0.00287028	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088415	TGAGGTCAAGTTCCC[A/G]TATGTAAGATTCCTT	2177
rs779689268	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10063698	AGCTTTGCCAGTAAA[A/T]TCAGAAAGTGAAAAA	2177
rs779740652	snp	A/G			missense	FANCD2	GRCh38.p7	3:10065938	AAAGAGCGTTCATTC[A/G]TGTGTTCTCTCATAT	2177
rs779746715	snp	C/G	1.74995e-05	0.00295795	missense	FANCD2	GRCh38.p7	3:10067218	TTGCAGATTGTAAAT[C/G]CCTTCTGCCAGGAAA	2177
rs779808366	snp	C/G/T	5.0009e-05	0.00500024	intron-variant	FANCD2	GRCh38.p7	3:10060407	GGCGGCAGACAGGTA[C/G/T]ACGTGGAGATTCTGA	2177
rs779824100	snp	A/C	3.36225e-05	0.00410001	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090268	CATCATGGTGTGGGC[A/C]CGCATGCTTTTCCCG	2177
rs779832229	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10077521	GATCATGCCACTGCC[C/T]TCCAGCCTGGGTGAC	2177
rs779894573	snp	C/T	1.77827e-05	0.00298178	intron-variant	FANCD2	GRCh38.p7	3:10046729	TCATTACTTAGTAAG[C/T]GTCAGAGACTATTGA	2177
rs779920070	snp	A/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090103	ATAAAGTTAATTCCA[A/T]TGTTTGACAGGCAAT	2177
rs779959665	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10045890	CAGGCGTGAGCCACC[A/G]TGCCTGGCCTAGTAA	2177
rs779959708	in-del	-/GCA			intron-variant	FANCD2	GRCh38.p7	3:10031372	CCGGGCGTGGTGGTG[-/GCA]TGCACCTGTAGTCCC	2177
rs779977236	snp	A/G/T	5.03608e-05	0.0050178	intron-variant	FANCD2	GRCh38.p7	3:10033022	AATGAAATAGTTCAG[A/G/T]ACTGAATCATGGGTT	2177
rs779994204	snp	C/G	1.66402e-05	0.00288441	intron-variant	FANCD2	GRCh38.p7	3:10036376	TGTTCAAAGTACCCT[C/G]ATGTACTTAAGTTCT	2177
rs779997353	snp	A/G	1.65146e-05	0.0028735	intron-variant	FANCD2	GRCh38.p7	3:10048082	TATTTTGGCAAGGAG[A/G]GAACACAGAAAGGGA	2177
rs780000481	snp	A/T	3.30393e-05	0.0040643	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098744	ATTAAGTCCCAAAAT[A/T]CCCAGGAGAGCACAG	2177
rs780002549	snp	C/T	1.65479e-05	0.0028764	missense	FANCD2	GRCh38.p7	3:10060303	TTGCAGGATGACATG[C/T]ACTTGGTGATAAGAA	2177
rs780011242	snp	C/T	0.000115596	0.00760164	intron-variant	FANCD2	GRCh38.p7	3:10073403	AGGTTTGTGACATCC[C/T]AGTGAGATTAACAGA	2177
rs780012176	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10058312	TGTTTTTCATCGCTG[A/G]CACCACGAAGGTTGC	2177
rs780018258	snp	A/C	1.65364e-05	0.0028754	missense	FANCD2	GRCh38.p7	3:10073279	AAAACAGATGGCAGC[A/C]AGACATCCTCCTCTG	2177
rs780033027	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10076710	ATGCCCCACTACACC[C/T]GGCTAGTTTTTTTAT	2177
rs780047608	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10044597	ATCTCAAAAGATAAA[A/G]AGCCGGATGATTGAG	2177
rs780080619	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10053952	CTGAAAAAGCCAGGC[C/T]GTAATCCCAGCACTT	2177
rs780098296	snp	C/G	3.29451e-05	0.00405851	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088906	CCCAGAACTGATCAA[C/G]TCTCCTAAAGATGCA	2177
rs780136280	snp	A/G			upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025216	CCACCTCAGCCTCCC[A/G]AAGTATTGAGATTAC	2177
rs780189396	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10038872	AGGCATGAGCCACTG[C/T]ATCTGACTTATGCTT	2177
rs780206352	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10030784	ACGTGTCTGTAATCT[C/T]AGCTACTCGGGAGGC	2177
rs780208317	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10068018	TGGGTATAGATCCAT[A/G]GCTACTATTAAACTG	2177
rs780226145	snp	A/G	1.64749e-05	0.00287005	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087097	TGTGACACATAGGAT[A/G]CTATTGCATTTGTTT	2177
rs780255660	snp	A/G	0.000162324	0.00900755	intron-variant	FANCD2	GRCh38.p7	3:10040556	TTCATTCTAATGCAC[A/G]GTCCTGCATCAGACC	2177
rs780267423	snp	A/T	1.65269e-05	0.00287457	intron-variant	FANCD2	GRCh38.p7	3:10039872	CTCTGTCATCATCTA[A/T]GTGAGGCTCAGCTAT	2177
rs780286320	snp	A/T	3.29592e-05	0.00405938	intron-variant	FANCD2	GRCh38.p7	3:10063768	GCAGCCCAAGGTTTA[A/T]ACCATTCTTCCTCTT	2177
rs780304251	snp	A/T	1.64814e-05	0.00287061	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088534	TGACCAGCTCCATGC[A/T]CTGCTCTGGTGAGAT	2177
rs780319584	snp	A/T	1.6473e-05	0.00286988	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094290	TCTCTCTTCTTCAGT[A/T]TGGGCGTCTCTTTGT	2177
rs780343756	snp	G/T	1.65299e-05	0.00287483	missense	FANCD2	GRCh38.p7	3:10032913	ATGACAGCATCTTTG[G/T]AAAGCTTCTTAAGAT	2177
rs780374375	snp	A/C	6.58946e-05	0.0057396	missense	FANCD2	GRCh38.p7	3:10048004	ATTTCATTTGGCAGT[A/C]TCCTATACAAATATG	2177
rs780384817	snp	C/T	1.66023e-05	0.00288113	intron-variant	FANCD2	GRCh38.p7	3:10046564	TTTTCTGTTGTTGCA[C/T]ATTTATTGACAATAG	2177
rs780442060	in-del	-/G	1.64773e-05	0.00287026	frameshift-variant	FANCD2	GRCh38.p7	3:10074607	AGAGCTGGACATTGA[-/G]GTCTTCTCTATTCTA	2177
rs780491203	snp	C/G	1.64942e-05	0.00287173	missense	FANCD2	GRCh38.p7	3:10052396	CCACAGGGCATTTTA[C/G]ATTATCTGGATAACA	2177
rs780499269	snp	A/G	1.64776e-05	0.00287028	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092229	GCTGTTCGAGACTTC[A/G]GTATCCTCATCAACT	2177
rs780505740	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094967	GGTAACCTATGTAAA[A/G]CTAAAATGCAGGTCT	2177
rs780536692	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10058679	AGGCTTATCTTTGAA[C/T]TCTGTATTCTATTTC	2177
rs780547790	snp	C/T	0.000280013	0.0118291	synonymous-codon	FANCD2	GRCh38.p7	3:10042639	GTTCATTCTTCATTC[C/T]GTAACAGCCATGGAT	2177
rs780573056	in-del	-/G	3.29473e-05	0.00405864	intron-variant	FANCD2	GRCh38.p7	3:10064679	GTGGTTTTCCCTGTA[-/G]CCTTGCGTATTCCTG	2177
rs780581041	snp	A/C	1.64977e-05	0.00287203	synonymous-codon	FANCD2	GRCh38.p7	3:10052482	CAAACAGAATGAAGC[A/C]AGCAGCCACATCCAG	2177
rs780581146	snp	C/T	3.46147e-05	0.00416006	intron-variant	FANCD2	GRCh38.p7	3:10043875	ACAAGGTAATGTTCA[C/T]GTACTATGCATTTTC	2177
rs780581588	snp	C/T	1.66181e-05	0.00288249	synonymous-codon	FANCD2	GRCh38.p7	3:10065871	TCTCTCAGATTGTCC[C/T]ATATTCCTAACTGAC	2177
rs780593607	snp	C/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094011	AGATAGAGCTCCCCT[C/G]TACTCTATGCTCTCA	2177
rs780651458	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10063692	ACATAGAGCTTTGCC[A/C]GTAAAATCAGAAAGT	2177
rs780651721	snp	C/T	1.64803e-05	0.00287052	intron-variant	FANCD2	GRCh38.p7	3:10047912	TCTACTCTTCCCCAC[C/T]CAAGGTTCTTAAGGA	2177
rs780654495	in-del	-/AAAA			intron-variant	FANCD2	GRCh38.p7	3:10041215	AAAAAACAAACAAAC[-/AAAA]AAAAAAGCAATCTAT	2177
rs780680176	snp	C/T	2.22878e-05	0.00333818	intron-variant	FANCD2	GRCh38.p7	3:10067346	CCTATACTGGTAGTA[C/T]TACTAGGCCAGTAGT	2177
rs780689400	snp	G/T	3.32369e-05	0.00407644	missense	FANCD2	GRCh38.p7	3:10049495	TGATGATGAATGCTG[G/T]CTTTGTAAAGGTATC	2177
rs780716256	in-del	-/TGT	1.66073e-05	0.00288156	intron-variant	FANCD2	GRCh38.p7	3:10064903	TTTCTTTTCTAAACC[-/TGT]TAGTGTTTTGAATGT	2177
rs780762477	snp	C/T	1.6473e-05	0.00286988	splice-donor-variant	FANCD2	GRCh38.p7	3:10064431	GTTGTTCCGGAAGGG[C/T]AGGTATTGTTTACCT	2177
rs780766282	snp	G/T	3.29478e-05	0.00405867	missense	FANCD2	GRCh38.p7	3:10064379	TGGGCATACCATCTG[G/T]AATGATTTCCAGGAT	2177
rs780767670	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10060575	TATATATTACCATGT[A/G]TATGTTTTGCTGGAA	2177
rs780773924	snp	C/T	1.64735e-05	0.00286993	missense	FANCD2	GRCh38.p7	3:10078175	TGACACCTCCTATTG[C/T]CAGGAGAGTCCCCTT	2177
rs780789790	snp	A/G	1.64741e-05	0.00286998	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096413	GTCAAAGCTATGCTC[A/G]CTCTCAACAATTGTA	2177
rs780825044	snp	C/G	5.01987e-05	0.00500967	intron-variant	FANCD2	GRCh38.p7	3:10035130	ATAAAAGCATTAAAA[C/G]AAGGAAAGCAAAGTG	2177
rs780840005	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10044901	TTGTATTCTTACTTT[G/T]TTTTCTTAACATTTT	2177
rs780846090	snp	A/G	2.28256e-05	0.0033782	intron-variant	FANCD2	GRCh38.p7	3:10062134	TAATAATTTAAAAAA[A/G]AATTCTTTGTTTTTA	2177
rs780867042	snp	C/G	1.64743e-05	0.00287	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088437	AGATTCCTTTGTCTT[C/G]TTTTCTAACAGCTTC	2177
rs780878229	snp	A/C	1.64822e-05	0.00287068	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10081507	CTGAGTATATACTTG[A/C]TTTTATTTGACAGTC	2177
rs780901607	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10058700	ATTCTATTTCATTGG[C/T]CTATACGTCTGTCCT	2177
rs780958584	snp	A/G	4.96356e-05	0.0049815	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096288	TGAAGGCATGATGAT[A/G]AACTCACAAAAGATG	2177
rs780958816	snp	A/C	3.30109e-05	0.00406256	synonymous-codon	FANCD2	GRCh38.p7	3:10072887	CACCCCAGACTATGT[A/C]CCTCCTCTTGGAAAC	2177
rs780963118	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10062562	CTTATAATGTGATTG[A/G]ATATGTTTATGAGTA	2177
rs780975075	snp	C/T			intron-variant, downstream-variant-500B	FANCD2, FANCD2OS	GRCh38.p7	3:10100020	GAGACCCCATCTCTA[C/T]AGAAAAAATTTTTTT	2177
rs781023139	snp	C/G	1.64743e-05	0.00287	missense	FANCD2	GRCh38.p7	3:10042661	GCCATGGATACACTT[C/G]AGGTATGCTCTTATA	2177
rs781038410	snp	G/T	1.75699e-05	0.00296389	intron-variant	FANCD2	GRCh38.p7	3:10046736	TTAGTAAGTGTCAGA[G/T]ACTATTGATTTTTAA	2177
rs781064333	snp	G/T	4.94246e-05	0.0049709	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087217	TCAGACTTTTGATGG[G/T]TATTTTGGAGAAATC	2177
rs781077760	snp	A/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088418	GGTCAAGTTCCCATA[A/T]GTAAGATTCCTTTGT	2177
rs781102924	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10050486	AAATTAGCCGGGCAT[A/C]GTGGCGGTCGCCTGT	2177
rs781102925	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10067931	GACAAAAACCACATG[A/G]TATTTAAATTGATGC	2177
rs781116092	in-del	-/A			intron-variant	FANCD2	GRCh38.p7	3:10069494	CCTCCCCCTCTCCCG[-/A]TCTCCCTCTGATGCC	2177
rs781126168	snp	C/T	5.0192e-05	0.00500934	intron-variant	FANCD2	GRCh38.p7	3:10043618	TGGAACTTTGATTAT[C/T]AAGGAGGAAATGAGT	2177
rs781127846	snp	A/G	3.31411e-05	0.00407056	missense	FANCD2	GRCh38.p7	3:10043504	CAGGAAATCAAGAAA[A/G]CAGCGGTCAGAGCTG	2177
rs781146006	snp	C/T	0.000200709	0.0100157	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090282	CACGCATGCTTTTCC[C/T]GTCTTCTAGGCATAC	2177
rs781168340	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087751	CCTCCCAGGTTCAAA[C/T]GATTCTCCTGCCTCA	2177
rs781210894	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10036073	CTCTAGTTGGAAAGA[A/G]AATTATACATTTCTT	2177
rs781223008	snp	C/T	4.94319e-05	0.00497127	intron-variant	FANCD2	GRCh38.p7	3:10039694	CTGGGTAATGTGCTG[C/T]AGTTCTAATAGTGTC	2177
rs781264177	snp	C/G	6.59674e-05	0.00574277	missense	FANCD2	GRCh38.p7	3:10064847	GCAAAAGATGGGGGT[C/G]CGGTGACCTCACAGG	2177
rs781266359	snp	C/G	1.64803e-05	0.00287052	missense	FANCD2	GRCh38.p7	3:10074589	TTCCCATGCTTTTTT[C/G]CGAGAGCTGGACATT	2177
rs781283708	snp	A/G			upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025017	CAATCGCAGTGGTGC[A/G]ATCATGGCTCACTTC	2177
rs781295854	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10075966	TCGATCTCCTGACCT[C/T]GTGATCCGCCCGCCT	2177
rs781304806	in-del	-/TGG	1.64735e-05	0.00286993	cds-indel	FANCD2	GRCh38.p7	3:10042569	TTTAGGTTCGCCAGT[-/TGG]TGATGGATAAGTTGT	2177
rs781335734	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10053797	GTCTGTTAGGGTAGA[G/T]ATGGGTCTGTGATCA	2177
rs781337668	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10080606	TTAAACCCCATCTCT[A/G]TAAAAAATACAAAAA	2177
rs781344292	snp	A/G	3.38221e-05	0.00411216	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090362	AAAAAAATTGAGCCT[A/G]GCACAGCAGCAGACT	2177
rs781344307	snp	C/T	1.65072e-05	0.00287286	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081276	AATATGAGGTTTCAT[C/T]TTTGGCTGAGAAAAA	2177
rs781378092	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10035823	CTCCTGAGAGCTCCC[C/T]TTGCAAGTTATTTGA	2177
rs781392128	in-del	-/TTTG			intron-variant	FANCD2	GRCh38.p7	3:10076725	CGGCTAGTTTTTTTA[-/TTTG]TTTGTTTGTTTGTTG	2177
rs781392236	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10030425	CTTAATGCCTTTGCA[G/T]TCTCATAGCTTAGCT	2177
rs781443140	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10042397	ATTAACAACTAAAAG[A/T]TTCTAATTTGGGGAA	2177
rs781445211	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10029007	TGTTGAGACACAAAG[A/G]CATAACATAGTCTGT	2177
rs781461714	snp	A/G	4.05466e-05	0.0045024	intron-variant	FANCD2	GRCh38.p7	3:10074487	AAATTCGATTAATAT[A/G]GAAGATTTATATATT	2177
rs781468026	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10061261	AGTGCTTTCTTGCAA[C/T]GTACTTTTATACTTT	2177
rs781513866	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10066892	ACCATGCCCAGCTAA[G/T]TTTTGTATTTTTGGT	2177
rs781516315	snp	A/G	1.72056e-05	0.00293301	intron-variant	FANCD2	GRCh38.p7	3:10043198	ATTTTCTGACATCCC[A/G]CTGTCAGAGTTAGAG	2177
rs781517919	snp	A/G	1.64814e-05	0.00287061	synonymous-codon	FANCD2	GRCh38.p7	3:10063902	TGAAAAGCTGGATCC[A/G]AAAGCCCTGGTAAAG	2177
rs781525182	snp	A/G	3.29549e-05	0.00405911	missense	FANCD2	GRCh38.p7	3:10041696	CTCCGACTTGACCCA[A/G]ACTTCCTATTGAAGG	2177
rs781540031	in-del	-/CA	1.6476e-05	0.00287014	intron-variant	FANCD2	GRCh38.p7	3:10078071	ACTAATCCTTTCCTC[-/CA]TGTGACAGGCTACAG	2177
rs781593257	in-del	-/AC			intron-variant	FANCD2	GRCh38.p7	3:10030879	CCTTCAGCCGGGGCA[-/AC]ACAGAGCAAGACTCT	2177
rs781605384	snp	C/T	1.64822e-05	0.00287068	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093300	GTATTTGATAGTCAT[C/T]CTGTTCTGCATGTAT	2177
rs781613701	snp	A/G	1.64732e-05	0.0028699	intron-variant	FANCD2	GRCh38.p7	3:10049370	TTGACTCTCCCCTGT[A/G]TAGGAAGTGGTTGGT	2177
rs781626176	snp	A/T	2.21305e-05	0.00332637	intron-variant	FANCD2	GRCh38.p7	3:10067190	TTGGAAGTATGAGAA[A/T]GTAATTTGTACTTTG	2177
rs781626919	snp	G/T	1.64727e-05	0.00286986	splice-acceptor-variant	FANCD2	GRCh38.p7	3:10046579	TATTTATTGACAATA[G/T]GTGTTTGACCTGGTG	2177
rs781650044	snp	A/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085329	TTTCTACTCTGATAC[A/T]TAGAGCTGTGATTGA	2177
rs781663600	in-del	-/CTC			intron-variant	FANCD2	GRCh38.p7	3:10073502	AGGCGTTGGAGTAAT[-/CTC]CTTAGTAGCAAAGTT	2177
rs781686867	in-del	-/T			intron-variant	FANCD2	GRCh38.p7	3:10036082	AAAGAGAATTATACA[-/T]TTTCTTTTTTTTTTT	2177
rs781692481	snp	A/G	1.64746e-05	0.00287002	synonymous-codon	FANCD2	GRCh38.p7	3:10046648	GAAGTACATTGACAG[A/G]GTGCTAAGAAATAAG	2177
rs781696088	snp	C/T	1.64822e-05	0.00287068	missense	FANCD2	GRCh38.p7	3:10063855	CAGGCCTCTGCACTT[C/T]ACTATGATGAATTTG	2177
rs781701459	snp	A/G	9.88338e-05	0.00702902	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094296	TTCTTCAGTATGGGC[A/G]TCTCTTTGTGGAAGC	2177
rs781704507	snp	G/T	1.65072e-05	0.00287286	missense	FANCD2	GRCh38.p7	3:10065901	CCTGGAGCCTGGAGA[G/T]AAGTTGGAGTCCATG	2177
rs781725867	in-del	-/TTCTT	1.64743e-05	0.00287	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088435	TAAGATTCCTTTGTC[-/TTCTT]TTCTAACAGCTTCCC	2177
rs781727393	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10033464	TTACTATGTCTTAAG[G/T]AAAGCATTTCTCATC	2177
rs796098710	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082751	TCTTCTAACACTCTG[A/G]TATCCGTTCGTGATA	2177
rs796113750	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10089139	AAAATACAAAAATTA[A/G]CCGGGCGTGGTGGCA	2177
rs796204302	in-del	-/G			intron-variant	FANCD2	GRCh38.p7	3:10051467	AAGTTGAAGATGGAG[-/G]CAGAGGCTATTGGCT	2177
rs796208455	in-del	-/TT			intron-variant	FANCD2	GRCh38.p7	3:10030097	TGGCCCATTATATCA[-/TT]TTTTTTTTTTTTTTT	2177
rs796212991	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10048864	TCTGTTATGACTATT[A/G]TGGAGTGACAGTATA	2177
rs796223701	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10048840	AGCTGTTGCAGTTGA[A/G]AATGTAATTCTGTTA	2177
rs796241281	in-del	-/A			intron-variant	FANCD2	GRCh38.p7	3:10031501	GCAAGACTCCATTTC[-/A]AAAAAAAAAAAAAAA	2177
rs796241964	multinucleotide-polymorphism	AAA/TAG			intron-variant	FANCD2	GRCh38.p7	3:10051449	AGTGTTGGACACTGA[AAA/TAG]AGTTGAAGATGGAGG	2177
rs796260891	multinucleotide-polymorphism	CA/GG			intron-variant	FANCD2	GRCh38.p7	3:10047624	ACTGGGATTTAGAAC[CA/GG]CTGGCCTCCAATCCC	2177
rs796268571	in-del	-/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097996	TTATAAGGTTTTTTT[-/T]AGTTGTCTGATTAGC	2177
rs796311023	in-del	-/A			intron-variant	FANCD2	GRCh38.p7	3:10051092	ACTGTCAAAAAAAAA[-/A]GAGTGAGGCCGGGCG	2177
rs796325129	multinucleotide-polymorphism	GCT/TCC			intron-variant	FANCD2	GRCh38.p7	3:10048422	ATTCTCCTGTCTCAG[GCT/TCC]CCTAAGTAGCTGTGA	2177
rs796356007	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10048844	GTTGCAGTTGAAAAT[A/G]TAATTCTGTTATGAC	2177
rs796371837	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10043345	TCAGATCAATCCCAG[A/G]CAGACGACAGTGCAA	2177
rs796374634	snp	G/T			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027010	AGTTCTGCCCGTGAT[G/T]ATGAGAATAATGGTA	2177
rs796405599	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10048871	TGACTATTATGGAGT[A/G]ACAGTATAAAGGGAG	2177
rs796450740	in-del	-/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092432	TTTTCTCACTAGGCA[-/T]TTTTTTTTTTGTCTT	2177
rs796498005	in-del	-/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092431	TTTTCTCACTAGGCA[-/T]TTTTTTTTTTTGTCT	2177
rs796549427	in-del	-/C			intron-variant	FANCD2	GRCh38.p7	3:10051434	GAGGGATTTATCTCC[-/C]AGTGTTGGACACTGA	2177
rs796639402	in-del	-/C			intron-variant	FANCD2	GRCh38.p7	3:10041843	ATTTGATATCTCTCT[-/C]TTTTTTTTTTTTTTC	2177
rs796652647	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10046728	TTCATTACTTAGTAA[G/T]TGTCAGAGACTATTG	2177
rs796653613	in-del	-/T			intron-variant	FANCD2	GRCh38.p7	3:10041842	CATTTGATATCTCTC[-/T]TTTTTTTTTTTTTTT	2177
rs796666228	snp	C/T			missense	FANCD2	GRCh38.p7	3:10073334	CAGAATGTGACCCTA[C/T]GCCATCTCATAGAGG	2177
rs796667495	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10089877	GTAGTCTTTTCAGTT[C/T]ATAAAGCACTTTCAC	2177
rs796796462	snp	C/T			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026945	CATCAAGAGTAAGTA[C/T]AGGTGGTGAAGAGCG	2177
rs796822389	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10067088	GTTGAGGACAGTTCT[A/G]TTACAGACTAAACTC	2177
rs796853918	in-del	-/T			intron-variant	FANCD2	GRCh38.p7	3:10030097	TGGCCCATTATATCA[-/T]TTTTTTTTTTTTTTT	2177
rs796857655	in-del	-/T			intron-variant	FANCD2	GRCh38.p7	3:10077573	AAAAAAATTTTTTTT[-/T]CACCCATTGGGAAGT	2177
rs796909828	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10048863	TTCTGTTATGACTAT[G/T]ATGGAGTGACAGTAT	2177
rs796952061	in-del	-/A			intron-variant	FANCD2	GRCh38.p7	3:10071148	AAAAAAGAAAAAAAG[-/A]AAAAAAAAAAAAGAT	2177
rs796977456	in-del	AA/G			intron-variant	FANCD2	GRCh38.p7	3:10071126	CAAGAATGATCGATA[AA/G]AAAAAAAAAAGAAAA	2177
rs796982404	in-del	-/CAAAAAGGAGT			intron-variant	FANCD2	GRCh38.p7	3:10051408	AAAAAAAAAAAAAAA[-/CAAAAAGGAGT]GAGGGATTTATCTCC	2177
rs796999436	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10061681	CTTAAAAAATATGTA[A/C]GAAAAAGAAAAAAGA	2177
rs797045572	in-del	-/T			intron-variant	FANCD2	GRCh38.p7	3:10063980	CACTCTTCAAGTCTT[-/T]CTGTTGCAGTGTGAA	2177

Page 1 | 2