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

DDB2

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs577284473	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47217763	GGATGTGGTGGTGTG[C/T]GCCTGTAGTCCCAGC	1643
rs577459290	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	DDB2, ACP2	GRCh38.p7	11:47239157	GGTGGTAGCAGAGGG[A/G]TCAAGCAGTTATTTG	1643
rs577486302	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47223081	AGTATAGAATTCTAG[A/G]TTCACAGTTTTTAAA	1643
rs577722796	snp	G/T	0.000399281	0.0141238	intron-variant	DDB2	GRCh38.p7	11:47236426	CTGCTAGTTCTGCAT[G/T]CTTTTCCAAAACTAC	1643
rs577926324	snp	C/G	0.000399281	0.0141238	intron-variant	DDB2	GRCh38.p7	11:47234035	CTGAATAGCAGGATC[C/G]CTGAAGCACCCTCCT	1643
rs577936729	snp	C/G	0.000399281	0.0141238	intron-variant	DDB2	GRCh38.p7	11:47226099	ATCCCTTTGAGACCC[C/G]GATTTCAGTTCTTTG	1643
rs578030151	snp	A/G	0.000399281	0.0141238	intron-variant	DDB2	GRCh38.p7	11:47233394	CTCTGGACTTCCCAA[A/G]AGAAAGTGGCTGGAG	1643
rs745328254	snp	A/T	1.64738e-05	0.00286995	intron-variant	DDB2	GRCh38.p7	11:47233008	TAAGCTTAGGTGTAG[A/T]TCCGGCAAGAGCATC	1643
rs745519132	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47233428	TTACAGAATGCGGCC[A/G]GGTGCAGTGGCTCAT	1643
rs745735733	snp	C/T	1.66004e-05	0.00288096	intron-variant	DDB2	GRCh38.p7	11:47216302	AAACCTTTCGTGAGA[C/T]TGGAGAGGAAAATAT	1643
rs745827778	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47227257	GATTACAGGCATGCG[C/T]CACCATGCCCGGCTA	1643
rs745977355	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47221772	TTTTGGTAGAAACAG[A/G]GTTTCACCATATTGG	1643
rs746073881	snp	C/T	1.64863e-05	0.00287104	intron-variant	DDB2	GRCh38.p7	11:47234717	CCCTCACCCCCACCT[C/T]GGTTCTGTGTCCCCA	1643
rs746180649	in-del	-/AAT			intron-variant	DDB2	GRCh38.p7	11:47217378	GAAACTCCATCTCAA[-/AAT]AATAATAATAATAAT	1643
rs746246270	in-del	-/CAAA			intron-variant	DDB2	GRCh38.p7	11:47218844	AGATGTGATTTTTCT[-/CAAA]CAAAGACACAAATCC	1643
rs746266024	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47229323	CTGAACCACAGGGAG[A/G]CCTAGAGTGGGGTGG	1643
rs746658321	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47221457	TTTGTTTTGTTTTGT[C/T]TTTTTAAGACAGAGT	1643
rs746711900	snp	A/C	1.64977e-05	0.00287203	missense, intron-variant, nc-transcript-variant	DDB2	GRCh38.p7	11:47235356	TCCCAGTGGGACTGC[A/C]CCCTGGGCCTGATCC	1643
rs746755700	snp	A/C	4.95831e-05	0.00497886	intron-variant	DDB2	GRCh38.p7	11:47238222	GACTTGCCAAGTCCG[A/C]TCCTACTTCCCAAGG	1643
rs746916266	snp	A/C			intron-variant	DDB2	GRCh38.p7	11:47229087	GTCATTAGGTAGGAT[A/C]AAGCAAGATAGATGT	1643
rs746985177	snp	A/G	1.64735e-05	0.00286993	intron-variant	DDB2	GRCh38.p7	11:47234524	CAACAGTGAGTAAAT[A/G]GGACTATCTCTGTCC	1643
rs747004341	snp	C/T			upstream-variant-2KB	DDB2	GRCh38.p7	11:47213009	TCCTGCCTGCCTCTT[C/T]GCAGAAACTAGGGTG	1643
rs747046524	snp	C/G	1.6486e-05	0.00287102	intron-variant	DDB2	GRCh38.p7	11:47234728	ACCTCGGTTCTGTGT[C/G]CCCACCTGAACCGAG	1643
rs747171370	snp	C/G	1.71475e-05	0.00292805	intron-variant	DDB2	GRCh38.p7	11:47216243	GAGACAGAGATTAAC[C/G]GTGCCGAATGAAACA	1643
rs747197122	snp	C/G			intron-variant	DDB2	GRCh38.p7	11:47215917	GCCTTCCTATTCCTT[C/G]TTTTCCTAAACGGTG	1643
rs747222465	snp	C/T	1.65203e-05	0.002874	missense, intron-variant	DDB2	GRCh38.p7	11:47234871	AAAATTTGGGACCTG[C/T]GCCAGGTTAGAGGGA	1643
rs747252946	snp	A/G			upstream-variant-2KB	DDB2	GRCh38.p7	11:47213687	TGAGTGTTGCGGCGC[A/G]CACCTGTAGTCCCAG	1643
rs747323146	snp	A/G	3.29788e-05	0.00406058	synonymous-codon, nc-transcript-variant	DDB2	GRCh38.p7	11:47216929	TGCCCCCTTTGACAG[A/G]AGGGCTACATCCTTG	1643
rs747323543	snp	A/T			utr-variant-5-prime, nc-transcript-variant	DDB2	GRCh38.p7	11:47215058	TTGTAGTCCCCGCCT[A/T]GTTTCTCCCCAGAGG	1643
rs747323551	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47231701	ATTTTTTTTGTGTGT[A/G]TAGAGATGGGGTCTC	1643
rs747541627	snp	G/T	4.95438e-05	0.00497689	intron-variant	DDB2	GRCh38.p7	11:47237800	CCCTTGATCATGTTC[G/T]GTGTTTACCCTCATG	1643
rs747546269	snp	A/G	5.1322e-05	0.00506541	intron-variant	DDB2	GRCh38.p7	11:47217066	TGAGCAGTTCCCCAT[A/G]CCAGGTCGTGCTAAA	1643
rs747619674	in-del	-/T	0.250331	0.25	intron-variant	DDB2	GRCh38.p7	11:47229819	ATTTGATGGCTCTTC[-/T]TTTTTTTTTTTTTTT	1643
rs747774067	snp	G/T	1.64808e-05	0.00287057	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47216950	TACATCCTTGGCGTG[G/T]CACCCAACTCACCCC	1643
rs747801559	snp	C/T	1.72907e-05	0.00294025	intron-variant	DDB2	GRCh38.p7	11:47217078	CATGCCAGGTCGTGC[C/T]AAAGAAGTGTTTGTT	1643
rs747856764	snp	C/G	3.29457e-05	0.00405854	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47237910	TCAAAAGTTGTACCC[C/G]TTATGAATTGAGGAC	1643
rs747893801	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47221677	CTTGAACTCCTGGCC[C/T]AAGGTGATCCACCTG	1643
rs747893909	snp	C/G			intron-variant	DDB2	GRCh38.p7	11:47238524	CTGCCTCAACCTCTC[C/G]AGTAGCTAGGACTAC	1643
rs748074787	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47223648	TTAGCCAGGCGTGGT[A/G]GTGGGCGCCTGTAGT	1643
rs748128394	snp	A/T	1.64817e-05	0.00287064	intron-variant	DDB2	GRCh38.p7	11:47234701	GGTCCTGCCTTTCCC[A/T]CCCTCACCCCCACCT	1643
rs748147583	snp	A/G	1.64808e-05	0.00287057	utr-variant-5-prime, nc-transcript-variant	DDB2	GRCh38.p7	11:47215112	CTTCGCATAGAGCAC[A/G]GTACCCCTTCACACG	1643
rs748397343	snp	A/G	1.65373e-05	0.00287548	intron-variant	DDB2	GRCh38.p7	11:47216327	AAATATGTCTGTTCT[A/G]CTTGGCAGGTCCTAG	1643
rs748422472	snp	G/T			intron-variant	DDB2	GRCh38.p7	11:47217930	CTTACCACATTGACC[G/T]CATCTTACGCCATTG	1643
rs748465633	in-del	-/A			intron-variant	DDB2	GRCh38.p7	11:47233697	TGGGCAACAAGAGCG[-/A]AAAATCTATCTCAAA	1643
rs748644904	snp	C/G	1.65299e-05	0.00287483	missense, intron-variant	DDB2	GRCh38.p7	11:47234881	ACCTGCGCCAGGTTA[C/G]AGGGAAAGCCAGCTT	1643
rs748705423	snp	C/G/T	8.54992e-05	0.00653782	intron-variant	DDB2	GRCh38.p7	11:47216248	AGAGATTAACCGTGC[C/G/T]GAATGAAACAAGGCT	1643
rs748730403	snp	A/G	1.64925e-05	0.00287158	intron-variant	DDB2	GRCh38.p7	11:47238021	GGCTTGGGTCCTCAA[A/G]TAATGATGGGAGGAA	1643
rs748760179	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47233310	GAATGCCCTGCACTC[A/G]CTGTGGTGTAATGAC	1643
rs748993672	snp	C/T	1.64727e-05	0.00286986	missense, intron-variant, nc-transcript-variant	DDB2	GRCh38.p7	11:47232853	GGGCTGAAGTTTAAC[C/T]CTCTCAATACCAACC	1643
rs749034260	snp	A/T	4.9458e-05	0.00497258	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47215219	GGAGCAGGAGTCCCC[A/T]GGAGCTGGAGCCCGA	1643
rs749226349	snp	A/C			intron-variant	DDB2	GRCh38.p7	11:47223671	CCTGTAGTCCCAGCT[A/C]CTTGGGAGGCTGAGG	1643
rs749269642	snp	C/G	1.72707e-05	0.00293855	intron-variant	DDB2	GRCh38.p7	11:47216223	GAAAGGCCGCAGGAG[C/G]TGATGAGACAGAGAT	1643
rs749281922	snp	C/G			upstream-variant-2KB	DDB2	GRCh38.p7	11:47213905	GAGCAGTGAGAACCA[C/G]ACACGGTGGCTCATG	1643
rs749409835	in-del	-/A			intron-variant	DDB2	GRCh38.p7	11:47225596	ACTCCATCTCTATTT[-/A]TAAAAAAAAAAAACA	1643
rs749426163	snp	C/T	1.65452e-05	0.00287616	synonymous-codon, nc-transcript-variant	DDB2	GRCh38.p7	11:47216445	CCAGCATAAGCTGGG[C/T]AGAGCTTCCTGGCCA	1643
rs749540520	snp	C/T			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	DDB2, ACP2	GRCh38.p7	11:47239037	CTCTGGACTTGCCTC[C/T]AGAGACTGCTCCAGA	1643
rs749565045	in-del	-/T			intron-variant	DDB2	GRCh38.p7	11:47237434	ACTGGCAAATACTAC[-/T]TTTTTTTTTTTTTTT	1643
rs749763301	snp	C/T	1.65302e-05	0.00287486	synonymous-codon, nc-transcript-variant	DDB2	GRCh38.p7	11:47216337	GTTCTGCTTGGCAGG[C/T]CCTAGCAGAAGATGT	1643
rs749770646	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47219292	CATGAAATTTACTTT[C/T]GTAACCATTTTAAAG	1643
rs749772795	snp	C/G			intron-variant	DDB2	GRCh38.p7	11:47218001	TATTCCTGAAACCGG[C/G]TCTCTGTAATTGCTG	1643
rs749806545	snp	C/T			synonymous-codon, intron-variant	DDB2	GRCh38.p7	11:47234861	TCAAACAGTGAAAAT[C/T]TGGGACCTGCGCCAG	1643
rs749887036	snp	A/T	1.67618e-05	0.00289493	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	DDB2, ACP2	GRCh38.p7	11:47238884	GGGCCAGACAAGGCC[A/T]TGGAGCCCACACATG	1643
rs749899157	snp	G/T			intron-variant	DDB2	GRCh38.p7	11:47236624	TCTAACTGATAGGGT[G/T]GTTGTGAAGATGAGT	1643
rs750210265	in-del	-/ATGAGACAGAGATTAACCGTGCCGA	1.72505e-05	0.00293682	intron-variant	DDB2	GRCh38.p7	11:47216226	AGGCCGCAGGAGGTG[-/ATGAGACAGAGATTAACCGTGCCGA]ATGAAACAAGGCTTC	1643
rs750238940	snp	C/G	4.94238e-05	0.00497086	synonymous-codon, intron-variant, nc-transcript-variant	DDB2	GRCh38.p7	11:47235298	CGATGGAGCCCGGCT[C/G]CTGACCACGGACCAG	1643
rs750322138	snp	C/G	3.32088e-05	0.00407471	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47216867	TGGCAGGGGCTCCAG[C/G]AGTCCTTTTTGCACA	1643
rs750406992	snp	C/G			intron-variant	DDB2	GRCh38.p7	11:47235209	GCAGGAGAAGGCCTG[C/G]AAGGCCAGGACCACA	1643
rs750489252	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47228028	TCCTGTCATCCCAGC[C/T]ACCCGGGAGGTTGAG	1643
rs750530703	snp	C/G	1.65743e-05	0.00287869	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47217036	TCAAGGACAAACCCA[C/G]CTTCATCAAAGGGGT	1643
rs750593401	snp	A/T	3.29462e-05	0.00405857	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47237958	GAAACTCAGGGAAGA[A/T]GATGTGTCAGCTCTA	1643
rs750653360	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47231590	GTGCAGTGATTCGAT[C/T]GCAACTCACTGCAGC	1643
rs750666045	snp	C/T	3.29549e-05	0.00405911	intron-variant	DDB2	GRCh38.p7	11:47232763	GCCCAGGCCTGGTTC[C/T]TCACGGCCAGGCCCA	1643
rs750667323	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47223313	AACATGGTGAAACCC[C/T]GCCTCTACTAAAAAT	1643
rs750753057	snp	A/T			intron-variant	DDB2	GRCh38.p7	11:47224019	GGTGGGAGAATTGCT[A/T]AAGCCCAGGGGGACA	1643
rs750851705	snp	C/T	1.6477e-05	0.00287024	synonymous-codon, nc-transcript-variant	DDB2	GRCh38.p7	11:47215190	CGAGATTGTATTACG[C/T]CCCAGGAACAAGAGG	1643
rs750932875	snp	C/T	1.64741e-05	0.00286998	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47237861	CATCCTCGCTACAAC[C/T]TCATTGTTGTGGGCC	1643
rs751023697	snp	A/C			intron-variant	DDB2	GRCh38.p7	11:47223340	AAATACAAAAATTAG[A/C]TGGGTGTGGTGGCGC	1643
rs751030002	snp	A/G			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	DDB2, ACP2	GRCh38.p7	11:47238974	AGGGTTGGAGCAGGG[A/G]TGCTGGGACCTGGGG	1643
rs751123153	snp	G/T	3.46398e-05	0.00416158	intron-variant	DDB2	GRCh38.p7	11:47216207	AGACCACACAGACAT[G/T]GAAAGGCCGCAGGAG	1643
rs751136580	snp	C/T	1.64779e-05	0.00287031	intron-variant	DDB2	GRCh38.p7	11:47234688	GTGCGTTCTCCGAGG[C/T]CCTGCCTTTCCCTCC	1643
rs751239207	snp	C/G	1.65078e-05	0.00287291	intron-variant	DDB2	GRCh38.p7	11:47238214	ATGTCTCTGACTTGC[C/G]AAGTCCGATCCTACT	1643
rs751334007	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47230981	AAAAATTAGCTGGGT[A/G]TGATGGTGTGGGCAT	1643
rs751334078	snp	A/G			upstream-variant-2KB	DDB2	GRCh38.p7	11:47214107	TCAGTGAAACTTGAG[A/G]TCAAGGCTGCAGTGA	1643
rs751422192	snp	G/T			intron-variant	DDB2	GRCh38.p7	11:47215625	CTCGGTGGTCAGTTG[G/T]GAGAGCCCCCAATTC	1643
rs751422435	snp	C/T	1.65395e-05	0.00287567	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47216891	TTGCACACTCTGGAT[C/T]CTTACCGGATATTAC	1643
rs751753400	snp	C/T	1.64727e-05	0.00286986	synonymous-codon, intron-variant, nc-transcript-variant	DDB2	GRCh38.p7	11:47232942	TCTACGAGTTTTTGC[C/T]AGCTCAGACACCATC	1643
rs751824557	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47238693	TTGAGCCACCGCGCC[C/T]GGCCTTCCTAGTATT	1643
rs751841814	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47217822	CTTGAACCCGGGAGG[C/T]GAAGGTTGCAGTGAG	1643
rs751910498	snp	A/G	1.64732e-05	0.0028699	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47237877	TCATTGTTGTGGGCC[A/G]ATACCCAGATCCTAA	1643
rs751957606	in-del	-/A			intron-variant	DDB2	GRCh38.p7	11:47230133	TGAGACCCTGTCTCT[-/A]AAAAAAAAAAAAAAA	1643
rs752136193	snp	C/T	1.64741e-05	0.00286998	synonymous-codon, nc-transcript-variant	DDB2	GRCh38.p7	11:47237974	GATGTGTCAGCTCTA[C/T]GACCCAGAATCTTCT	1643
rs752177163	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47226167	GTAATTTTGTTGTTC[A/G]TTTTTTGAGGAACCG	1643
rs752258696	snp	A/G	3.29625e-05	0.00405958	synonymous-codon, nc-transcript-variant	DDB2	GRCh38.p7	11:47238001	TTCTGGCATCAGTTC[A/G]GTGAGGCTTGGGTCC	1643
rs752297564	snp	A/G	1.68724e-05	0.00290446	intron-variant	DDB2	GRCh38.p7	11:47216271	ACAAGGCTTCCTTTC[A/G]GGGAATTCAGCAGAA	1643
rs752312065	snp	G/T	1.73132e-05	0.00294216	intron-variant	DDB2	GRCh38.p7	11:47216213	CACAGACATGGAAAG[G/T]CCGCAGGAGGTGATG	1643
rs752318717	snp	C/G			downstream-variant-500B	DDB2, ACP2	GRCh38.p7	11:47239235	TTCTGCGTGGATCTT[C/G]CAGAAGTGACCTGGT	1643
rs752406698	snp	G/T			intron-variant	DDB2	GRCh38.p7	11:47224965	TTTTTTGAGATGAGG[G/T]CTCACTCTCTCTTCC	1643
rs752647454	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47231388	GTAATGGAATACCTC[A/G]GCAATAAAATGAGAT	1643
rs752658655	snp	C/T	3.29652e-05	0.00405974	synonymous-codon, intron-variant	DDB2	GRCh38.p7	11:47234802	GTGACGCATGTGGCC[C/T]TGAACCCATGCTGTG	1643
rs752780570	snp	C/G			intron-variant	DDB2	GRCh38.p7	11:47216188	TTATTTCTGGTGCTC[C/G]TTGAGACCACACAGA	1643
rs752893080	snp	A/G	1.68388e-05	0.00290158	missense, intron-variant, nc-transcript-variant	DDB2	GRCh38.p7	11:47235407	CAGCACCTCACACCC[A/G]TCAAGGTGAGTGGCG	1643
rs752930885	snp	A/C			intron-variant	DDB2	GRCh38.p7	11:47220681	ACCTGTCTGGTTTTA[A/C]TCCCAGATGCTGACA	1643
rs752941806	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47219145	AGATGGGGTTTCACC[A/G]TGTTAGCCACGATGG	1643
rs752946218	snp	C/G	1.64762e-05	0.00287016	missense, intron-variant, nc-transcript-variant	DDB2	GRCh38.p7	11:47235313	CCTGACCACGGACCA[C/G]AAGAGCGAGATCCGA	1643
rs752976285	in-del	-/A			intron-variant	DDB2	GRCh38.p7	11:47232485	ACAAAACCCCATCTT[-/A]AAAAAAAAAAAATAG	1643
rs753060987	in-del	-/ATCT			intron-variant	DDB2	GRCh38.p7	11:47236826	TGTTCCCGATAATCC[-/ATCT]GTCTGCATGTCCCAG	1643
rs753070223	snp	C/T	3.29451e-05	0.00405851	synonymous-codon, intron-variant, nc-transcript-variant	DDB2	GRCh38.p7	11:47234589	ATCTGGTTTTGTAGC[C/T]TGGATGTGTCTGCTA	1643
rs753162529	snp	A/G	2.42386e-05	0.00348119	intron-variant	DDB2	GRCh38.p7	11:47238187	CCTCTGCAATGGGTG[A/G]GTAGGAGGAGAATGT	1643
rs753327018	in-del	-/TTTTTTTTTTTTT			intron-variant	DDB2	GRCh38.p7	11:47226736	TCAAGTCCTTTGCCT[-/TTTTTTTTTTTTT]TTTTTTTTTTTGAAA	1643
rs753467757	snp	A/C	1.6531e-05	0.00287493	synonymous-codon, nc-transcript-variant	DDB2	GRCh38.p7	11:47216400	CCCACAGATCCTGCC[A/C]CCATGCCGCAGCATC	1643
rs753753999	snp	G/T	3.33912e-05	0.00408589	intron-variant	DDB2	GRCh38.p7	11:47234938	CTGTCAACGCAGGTG[G/T]GATATCCCAGACCTC	1643
rs753782504	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47218510	TATTAGATAAATGGA[A/G]AGAAAAGAAGGAAAG	1643
rs753823942	snp	C/G			intron-variant	DDB2	GRCh38.p7	11:47230263	CAGGATTGCACCACT[C/G]CATCAAGGTTTTGAA	1643
rs753931064	snp	C/T	4.94181e-05	0.00497057	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47237925	CTTATGAATTGAGGA[C/T]GATCGACGTGTTCGA	1643
rs754089464	snp	G/T			intron-variant	DDB2	GRCh38.p7	11:47222777	GTGTGGATATATGTT[G/T]TCATTTTTCTTGGGT	1643
rs754091903	snp	C/G	1.65162e-05	0.00287365	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47216906	TCTTACCGGATATTA[C/G]AAAAGGCTGCCCCCT	1643
rs754161306	in-del	-/CTGGGGCTTGAAC			intron-variant	DDB2	GRCh38.p7	11:47215675	ATTCTCTGAGGTTTA[-/CTGGGGCTTGAAC]CTGGGGCTATAAGGA	1643
rs754254385	snp	A/G	1.64757e-05	0.00287012	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47215165	AACGCCCAGAAACCC[A/G]GAAGACCTCCGAGAT	1643
rs754261384	snp	A/G	1.64727e-05	0.00286986	missense, intron-variant, nc-transcript-variant	DDB2	GRCh38.p7	11:47234622	AGCCGAATGGTGGTC[A/G]CAGGAGACAACGTGG	1643
rs754405766	snp	C/G	1.64781e-05	0.00287033	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47215199	ATTACGCCCCAGGAA[C/G]AAGAGGAGCAGGAGT	1643
rs754458845	snp	C/G	1.64776e-05	0.00287028	intron-variant	DDB2	GRCh38.p7	11:47234689	TGCGTTCTCCGAGGT[C/G]CTGCCTTTCCCTCCC	1643
rs754557828	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47224747	TCCCTCCCTCCCTCC[C/T]TCCCTTCGTTCCTTT	1643
rs754672323	snp	A/C			intron-variant	DDB2	GRCh38.p7	11:47235979	GCTCTGTCACCCAGG[A/C]TGGAGTGCAGTGGCA	1643
rs754707377	snp	A/C	1.73165e-05	0.00294244	intron-variant	DDB2	GRCh38.p7	11:47216209	ACCACACAGACATGG[A/C]AAGGCCGCAGGAGGT	1643
rs754807593	in-del	-/GGGACGTTGAGGTGGAA			intron-variant	DDB2	GRCh38.p7	11:47230055	CTGTAACAGCACTTT[-/GGGACGTTGAGGTGGAA]GGGACGTTGAGGTGG	1643
rs755006840	snp	A/G	1.64738e-05	0.00286995	missense, intron-variant, nc-transcript-variant	DDB2	GRCh38.p7	11:47234660	GATCCTGCTGAACAT[A/G]GACGGCAAAGAGGTG	1643
rs755139917	snp	A/C			intron-variant	DDB2	GRCh38.p7	11:47217893	GAGACTCCATCTCAA[A/C]AAAAAAGAATTGAAG	1643
rs755246751	snp	A/G	1.64789e-05	0.0028704	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47237997	AATCTTCTGGCATCA[A/G]TTCGGTGAGGCTTGG	1643
rs755367611	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47233085	GATGTCAGCCACTTT[C/T]CGCCCTTCTTTCTCT	1643
rs755370586	snp	C/G	3.29457e-05	0.00405854	stop-gained, nc-transcript-variant	DDB2	GRCh38.p7	11:47237881	TGTTGTGGGCCGATA[C/G]CCAGATCCTAATTTC	1643
rs755446513	snp	C/T			upstream-variant-2KB	DDB2	GRCh38.p7	11:47213278	AGCATTTTGGGAGGC[C/T]GAGGCAGGCAGATCA	1643
rs755579233	snp	G/T	1.64738e-05	0.00286995	intron-variant	DDB2	GRCh38.p7	11:47232794	TCATCACTCACTGGC[G/T]TTTTCCTTCCTCGTG	1643
rs755633984	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47223222	GGGCGCTGTGGCTTA[C/T]GCCTGTAATCCCAGC	1643
rs755646110	snp	A/T	3.35965e-05	0.00409843	intron-variant	DDB2	GRCh38.p7	11:47216276	GCTTCCTTTCGGGGA[A/T]TTCAGCAGAAAAACC	1643
rs755700924	snp	C/T	3.46266e-05	0.00416078	intron-variant	DDB2	GRCh38.p7	11:47216215	CAGACATGGAAAGGC[C/T]GCAGGAGGTGATGAG	1643
rs755704153	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47232204	TACAATTTAGCCATG[C/T]GTGGTGGTGGGCACC	1643
rs755783429	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47226450	GGCTAATTTTTGTAT[C/T]TTCAGTAGAGACGGG	1643
rs755842160	in-del	-/A/AA/AAA			upstream-variant-2KB	DDB2	GRCh38.p7	11:47213510	GTGAGACTCCGTCTC[-/A/AA/AAA]AAAAAAAAAAAAAAA	1643
rs755880983	in-del	-/T	4.48702e-05	0.00473636	intron-variant	DDB2	GRCh38.p7	11:47229760	CAGATTCCTTTTACA[-/T]TTTTATTACCTTAAT	1643
rs755924189	snp	C/T	1.64825e-05	0.00287071	intron-variant	DDB2	GRCh38.p7	11:47234702	GTCCTGCCTTTCCCT[C/T]CCTCACCCCCACCTC	1643
rs755944523	snp	G/T			intron-variant	DDB2	GRCh38.p7	11:47215825	CAAATACAGTTTGGT[G/T]ATCAGGAGTTGTTGC	1643
rs756007003	snp	A/G			downstream-variant-500B	DDB2, ACP2	GRCh38.p7	11:47239266	CAGAGAGCTTCTTGC[A/G]TCTCAGAAATGAAGA	1643
rs756188946	snp	G/T	1.64838e-05	0.00287083	missense, intron-variant	DDB2	GRCh38.p7	11:47234821	ACCCATGCTGTGATT[G/T]GTTCCTGGCCACAGC	1643
rs756300143	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47220745	AGCAACAGTGCCTCA[C/T]TTTGTCACTTCTTTA	1643
rs756313355	snp	C/T	1.65323e-05	0.00287505	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47216897	ACTCTGGATTCTTAC[C/T]GGATATTACAAAAGG	1643
rs756332364	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47229202	TGGCAGCTCAGTACA[C/T]AGAGACTGGGCCCAA	1643
rs756368265	snp	A/C	1.65362e-05	0.00287538	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47216431	GTCAGGACCCTCCAC[A/C]AGCATAAGCTGGGCA	1643
rs756368274	snp	G/T	1.73646e-05	0.00294652	splice-donor-variant, intron-variant	DDB2	GRCh38.p7	11:47235413	CTCACACCCATCAAG[G/T]TGAGTGGCGGTGGGA	1643
rs756371187	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47225839	TTGACTACTTTAGAT[A/G]TCTCATCTAAGTGGA	1643
rs756478101	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47219166	GCCACGATGGTCTCT[A/G]TCTCCTGACCTTGTG	1643
rs756484790	snp	A/G	4.97104e-05	0.00498525	intron-variant	DDB2	GRCh38.p7	11:47238192	GCAATGGGTGAGTAG[A/G]AGGAGAATGTCTCTG	1643
rs756577985	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47233241	GATAAGCCAGCATGG[C/T]GTGGACCCAGAAAGC	1643
rs756657410	in-del	-/TTTTTTTTTTTTTT			intron-variant	DDB2	GRCh38.p7	11:47226735	TTCAAGTCCTTTGCC[-/TTTTTTTTTTTTTT]TTTTTTTTTTTGAAA	1643
rs756739840	snp	A/C/G	3.05572e-05	0.00390867	intron-variant	DDB2	GRCh38.p7	11:47238213	AATGTCTCTGACTTG[A/C/G]CAAGTCCGATCCTAC	1643
rs756792852	snp	A/G	1.65089e-05	0.00287301	intron-variant	DDB2	GRCh38.p7	11:47238033	CAAATAATGATGGGA[A/G]GAAGCAGGGATTCAA	1643
rs756798662	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47228383	CGGTGGCTCACTCCT[A/G]TAATCTCAGCACTTT	1643
rs756968720	snp	C/T	3.331e-05	0.00408092	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	DDB2, ACP2	GRCh38.p7	11:47238866	AGACACTAAAGAAGG[C/T]GTGGGCCAGACAAGG	1643
rs756970973	snp	C/G	1.64738e-05	0.00286995	intron-variant	DDB2	GRCh38.p7	11:47233001	GGGCTTCTAAGCTTA[C/G]GTGTAGTTCCGGCAA	1643
rs757030681	snp	A/G	1.67052e-05	0.00289004	intron-variant	DDB2	GRCh38.p7	11:47234939	TGTCAACGCAGGTGT[A/G]ATATCCCAGACCTCA	1643
rs757073569	snp	C/T	5.17228e-05	0.00508515	intron-variant	DDB2	GRCh38.p7	11:47216227	GGCCGCAGGAGGTGA[C/T]GAGACAGAGATTAAC	1643
rs757099083	snp	A/G			downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	DDB2, ACP2	GRCh38.p7	11:47239514	TCCCAAGTACAGACA[A/G]CCTTCCGTCCTGCTC	1643
rs757139403	snp	C/G			intron-variant	DDB2	GRCh38.p7	11:47226643	GTTTCATTTGCATTT[C/G]TCTAATGATTAGTGA	1643
rs757212062	snp	A/C			intron-variant	DDB2	GRCh38.p7	11:47231619	GCCTCGACCTCCAGG[A/C]TTCCGTCATCTTCCC	1643
rs757228612	in-del	-/C	1.64836e-05	0.0028708	utr-variant-5-prime, nc-transcript-variant	DDB2	GRCh38.p7	11:47215124	CACAGTACCCCTTCA[-/C]ACGGAGGACGCGATG	1643
rs757304535	snp	C/G	1.66676e-05	0.00288679	intron-variant	DDB2	GRCh38.p7	11:47216291	ATTCAGCAGAAAAAC[C/G]TTTCGTGAGATTGGA	1643
rs757335768	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47230533	GGTTTGAGAACAACT[A/G]CAACCAACCCTTGGT	1643
rs757364158	snp	C/G	1.86649e-05	0.00305485	intron-variant	DDB2	GRCh38.p7	11:47235433	TGGCGGTGGGAAGGA[C/G]CTCGCAGAAGGAGGC	1643
rs757390197	in-del	-/TGGC			downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	DDB2, ACP2	GRCh38.p7	11:47239606	AGACACAGGGAAATG[-/TGGC]TGGCTGGCTGGCTGT	1643
rs757461854	snp	A/C	3.29875e-05	0.00406112	synonymous-codon, nc-transcript-variant	DDB2	GRCh38.p7	11:47217001	CAAAGGGGGAGATAT[A/C]ATGCTCTGGAATTTT	1643
rs757474556	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47217168	ATCACCTGAGGTATG[A/G]AGTTTGAGACCAGCC	1643
rs757732012	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47223078	CTAAGTATAGAATTC[C/T]AGGTTCACAGTTTTT	1643
rs757762991	snp	C/T	1.64871e-05	0.00287111	synonymous-codon, intron-variant, nc-transcript-variant	DDB2	GRCh38.p7	11:47235340	CCGAGTTTACTCTGC[C/T]TCCCAGTGGGACTGC	1643
rs757768415	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47236536	AGCAGCCAGACCCCC[C/T]GGGTTAGAATCCTTG	1643
rs757824053	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47236700	ACTGGTAAGTATTCA[A/G]TAAATGATGATTGAA	1643
rs757860656	snp	C/G			intron-variant	DDB2	GRCh38.p7	11:47221046	TGCACGTCTGTAGTT[C/G]CAGCTACTCAGGAAT	1643
rs757905578	in-del	-/AGAG			upstream-variant-2KB	DDB2	GRCh38.p7	11:47214603	CAGAAAAAGAAAAAA[-/AGAG]AGAGAGAGAGAGAAA	1643
rs757932781	in-del	-/A			upstream-variant-2KB	DDB2	GRCh38.p7	11:47213303	AGATCACAAGGTCAG[-/A]AGATCGAGACCATCC	1643
rs758089001	snp	C/T	4.94507e-05	0.00497221	utr-variant-5-prime, nc-transcript-variant	DDB2	GRCh38.p7	11:47215100	TCCCTCCATGATCTT[C/T]GCATAGAGCACAGTA	1643
rs758105053	snp	A/C	3.29538e-05	0.00405904	intron-variant	DDB2	GRCh38.p7	11:47234685	GAGGTGCGTTCTCCG[A/C]GGTCCTGCCTTTCCC	1643
rs758139129	snp	C/T	8.27328e-05	0.00643114	intron-variant	DDB2	GRCh38.p7	11:47216320	GAGAGGAAAATATGT[C/T]TGTTCTGCTTGGCAG	1643
rs758168272	snp	C/G	1.65307e-05	0.0028749	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47216415	ACCATGCCGCAGCAT[C/G]GTCAGGACCCTCCAC	1643
rs758199547	snp	C/T	1.64754e-05	0.00287009	synonymous-codon, intron-variant, nc-transcript-variant	DDB2	GRCh38.p7	11:47235304	AGCCCGGCTCCTGAC[C/T]ACGGACCAGAAGAGC	1643
rs758285471	snp	A/T			intron-variant	DDB2	GRCh38.p7	11:47224872	TTCAGATACTGTATA[A/T]CCCCTCTAGAAGTTT	1643
rs758435294	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47228875	GGCTGGAGAATTGTT[C/T]AAACCCAGGAGGCGG	1643
rs758545373	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47231660	TCTGAGTAGCTAGAA[C/T]CACATGCACCTACCA	1643
rs758638428	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47233012	CTTAGGTGTAGTTCC[A/G]GCAAGAGCATCCAGA	1643
rs758661897	snp	A/C			upstream-variant-2KB	DDB2	GRCh38.p7	11:47213568	GTGGCTCACACCTGT[A/C]ATCTCAGCACTTTGG	1643
rs758666064	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47215869	TAATTTCACTTACCT[C/T]CCCAGAAGTAACCTA	1643
rs758703538	in-del	-/TT	7.61513e-05	0.00617008	intron-variant	DDB2	GRCh38.p7	11:47238126	CTCATGTTGACACTC[-/TT]GTCTCTGCAGCTTAA	1643
rs758816557	snp	A/C	1.93613e-05	0.00311131	intron-variant	DDB2	GRCh38.p7	11:47235445	GGAGCTCGCAGAAGG[A/C]GGCTGTGATCATGAG	1643
rs758898579	snp	A/T	1.65051e-05	0.00287267	synonymous-codon, nc-transcript-variant	DDB2	GRCh38.p7	11:47216914	GATATTACAAAAGGC[A/T]GCCCCCTTTGACAGG	1643
rs758915118	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47223370	CTCACCAGTAATCCC[A/G]GCTACCCGGGAGGCT	1643
rs759389471	snp	C/T	1.64846e-05	0.0028709	intron-variant	DDB2	GRCh38.p7	11:47237830	GGCCGGCCTCTCCAT[C/T]TCCTAGGCAGCCTGG	1643
rs759521227	snp	C/T	0.000108816	0.00737537	intron-variant	DDB2	GRCh38.p7	11:47217101	TGTTTGTTGGCTGGG[C/T]GCAGTGGTTCGCACC	1643
rs759607243	in-del	-/TT/TTT/TTTT			intron-variant	DDB2	GRCh38.p7	11:47226278	CCAACATTTATTTTC[-/TT/TTT/TTTT]TTTTTTTTTTTTTTT	1643
rs759622121	snp	C/T	3.29457e-05	0.00405854	synonymous-codon, intron-variant, nc-transcript-variant	DDB2	GRCh38.p7	11:47234588	CATCTGGTTTTGTAG[C/T]CTGGATGTGTCTGCT	1643
rs759657658	snp	A/C			intron-variant	DDB2	GRCh38.p7	11:47231098	GCACTTCAGCCTGGG[A/C]GACAGAGCAAGCCTT	1643
rs759662245	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47220485	CAAGTGCTTTGAACT[C/T]GTGCCAGACTGAGAT	1643
rs759712905	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47235660	TCAGCCCAGCTCTGA[C/T]CTCACTGTGAGAATT	1643
rs759835280	snp	C/T	1.64836e-05	0.0028708	utr-variant-5-prime, nc-transcript-variant	DDB2	GRCh38.p7	11:47215122	AGCACAGTACCCCTT[C/T]ACACGGAGGACGCGA	1643
rs759879517	snp	C/T	1.65236e-05	0.00287429	synonymous-codon, nc-transcript-variant	DDB2	GRCh38.p7	11:47216355	TAGCAGAAGATGTGA[C/T]TCAGACTGCCTCTGG	1643
rs759948056	snp	C/T	1.64999e-05	0.00287222	intron-variant	DDB2	GRCh38.p7	11:47238790	GTCAGACTGGTCTCA[C/T]TCTTCCTAGGTTACC	1643
rs760094371	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47227895	GCCTGTAATTCCAGC[A/G]CTTTGGGAGGCCGAG	1643
rs760106847	snp	A/G	1.64727e-05	0.00286986	missense, intron-variant, nc-transcript-variant	DDB2	GRCh38.p7	11:47232944	TACGAGTTTTTGCCA[A/G]CTCAGACACCATCAA	1643
rs760218112	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47227967	CAACATGGTGAAACC[C/T]CGTCTCTACTAAATA	1643
rs760275244	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47220030	TCCTGACCTCGTGAT[C/T]CGCCCGCCTCGACCT	1643
rs760285687	in-del	-/TTTTTTTTTTTT			intron-variant	DDB2	GRCh38.p7	11:47226737	CAAGTCCTTTGCCTT[-/TTTTTTTTTTTT]TTTTTTTTTTTGAAA	1643
rs760319850	snp	C/T			downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	DDB2, ACP2	GRCh38.p7	11:47239655	GGGAGCCAATGTTTG[C/T]ACCCCTGGTATTAGC	1643
rs760322280	snp	A/C	1.64727e-05	0.00286986	missense, intron-variant, nc-transcript-variant	DDB2	GRCh38.p7	11:47232890	ACGCCTCCTCAATGG[A/C]GGGAACAACTAGGCT	1643
rs760403412	snp	A/G	1.68233e-05	0.00290023	intron-variant	DDB2	GRCh38.p7	11:47216814	TGGCAGTTTACCCAG[A/G]ACTTGGGTTTTAATT	1643
rs760456614	snp	A/G	1.65291e-05	0.00287476	synonymous-codon, nc-transcript-variant	DDB2	GRCh38.p7	11:47216391	GCTGGCTGGCCCACA[A/G]ATCCTGCCACCATGC	1643
rs760490269	in-del	-/AAAAA			intron-variant	DDB2	GRCh38.p7	11:47223625	CTGTTCTAAAAATAC[-/AAAAA]AAATTAGCCAGGCGT	1643
rs760495922	snp	A/G	1.65715e-05	0.00287845	missense, intron-variant, nc-transcript-variant	DDB2	GRCh38.p7	11:47235384	TCCCGCACCCTCACC[A/G]TCACTTCCAGCACCT	1643
rs760526475	in-del	-/TCA	1.65086e-05	0.00287298	cds-indel, downstream-variant-500B, nc-transcript-variant	DDB2, ACP2	GRCh38.p7	11:47238812	TAGGTTACCACATTC[-/TCA]TCTGGAGCCAGGAGG	1643
rs760603070	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47232676	AGGCCCTGTAGAGAG[C/T]GTCCTAGTGTCTAAG	1643
rs760606007	snp	C/T	1.6477e-05	0.00287024	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47215143	GAGGACGCGATGGCT[C/T]CCAAGAAACGCCCAG	1643
rs760651900	in-del	-/AT			intron-variant	DDB2	GRCh38.p7	11:47229684	CTTTGAATTGAAGAC[-/AT]TGATACAAATTTAAG	1643
rs760697461	snp	A/C			intron-variant	DDB2	GRCh38.p7	11:47217420	AAAATAAAAATAAGG[A/C]GTGTTTGTTGAAGGC	1643
rs760857478	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47223766	AGCCTGGGTGACAGA[A/G]CAAGACTCCGTCTAA	1643
rs760979102	snp	C/G	1.65192e-05	0.00287391	missense, downstream-variant-500B, nc-transcript-variant	DDB2, ACP2	GRCh38.p7	11:47238825	TCTCATCTGGAGCCA[C/G]GAGGAAGCCAGGACA	1643
rs761172736	snp	C/T			upstream-variant-2KB	DDB2	GRCh38.p7	11:47213337	CCAACATGGTGAAAC[C/T]CTGTCTCTACTAAAA	1643
rs761282021	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47230810	AGAACTTTACATCTT[A/G]GGGATGTAAAGTTCT	1643
rs761285630	snp	A/T	1.64727e-05	0.00286986	synonymous-codon, intron-variant, nc-transcript-variant	DDB2	GRCh38.p7	11:47234612	GTCTGCTAGTAGCCG[A/T]ATGGTGGTCACAGGA	1643
rs761316617	snp	A/G	1.66674e-05	0.00288676	intron-variant	DDB2	GRCh38.p7	11:47216854	TCATTTCTCTCTGTG[A/G]CAGGGGCTCCAGCAG	1643
rs761555714	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47229500	GCATCCTAAGGAAGA[C/T]GTGCATTTGGGGAGT	1643
rs761699363	snp	A/C/G	6.58984e-05	0.00573983	missense, intron-variant, nc-transcript-variant	DDB2	GRCh38.p7	11:47235294	GTCCCGATGGAGCCC[A/C/G]GCTCCTGACCACGGA	1643
rs761726803	snp	A/G	0.000160486	0.00895642	intron-variant	DDB2	GRCh38.p7	11:47235422	ATCAAGGTGAGTGGC[A/G]GTGGGAAGGAGCTCG	1643
rs761745373	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47220248	GAGTGCCGCGGACAG[A/G]GTGGGGTAGGTTTCC	1643
rs761752334	snp	A/G	1.64754e-05	0.00287009	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47237853	CAGCCTGGCATCCTC[A/G]CTACAACCTCATTGT	1643
rs761800666	snp	C/G			intron-variant	DDB2	GRCh38.p7	11:47218790	GTCAGGGGTAAACTA[C/G]AGATGACTGTTGTGC	1643
rs761833288	in-del	-/C	1.64749e-05	0.00287005	frameshift-variant, intron-variant, nc-transcript-variant	DDB2	GRCh38.p7	11:47235296	CCCGATGGAGCCCGG[-/C]TCCTGACCACGGACC	1643
rs761952259	in-del	-/T			intron-variant	DDB2	GRCh38.p7	11:47223139	TAAATTAAAATTGTA[-/T]TTTATTGCATACAAT	1643
rs762017413	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47225579	CCTGGGCAACAGAGC[A/G]AGACTCCATCTCTAT	1643
rs762129958	snp	C/T	1.64784e-05	0.00287035	intron-variant	DDB2	GRCh38.p7	11:47234683	AAGAGGTGCGTTCTC[C/T]GAGGTCCTGCCTTTC	1643
rs762306884	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47238797	TGGTCTCACTCTTCC[C/T]AGGTTACCACATTCT	1643
rs762359144	snp	C/T	8.24192e-05	0.00641894	intron-variant	DDB2	GRCh38.p7	11:47234733	GGTTCTGTGTCCCCA[C/T]CTGAACCGAGCTCTT	1643
rs762435826	snp	A/G	3.29511e-05	0.00405887	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47215167	CGCCCAGAAACCCAG[A/G]AGACCTCCGAGATTG	1643
rs762496558	snp	A/G	3.2963e-05	0.00405961	missense, intron-variant	DDB2	GRCh38.p7	11:47234772	CTTTGGAATCTCAGA[A/G]TGCACAAAAAGAAAG	1643
rs762693320	snp	C/T	1.65721e-05	0.0028785	synonymous-codon, intron-variant, nc-transcript-variant	DDB2	GRCh38.p7	11:47235385	CCCGCACCCTCACCG[C/T]CACTTCCAGCACCTC	1643
rs762843794	snp	C/T	1.6591e-05	0.00288015	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47216870	CAGGGGCTCCAGCAG[C/T]CCTTTTTGCACACTC	1643
rs762875417	snp	A/C			intron-variant	DDB2	GRCh38.p7	11:47221890	CCGGCCTGGGTTTTT[A/C]AAATTATATCTTTAT	1643
rs762943470	snp	C/G	1.64784e-05	0.00287035	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47216963	TGGCACCCAACTCAC[C/G]CCAGCACTGTGGCTG	1643
rs763083097	snp	A/G	1.99507e-05	0.00315832	synonymous-codon, nc-transcript-variant	DDB2	GRCh38.p7	11:47238146	TCTGCAGCTTAATGA[A/G]TTCAATCCCATGGGG	1643
rs763142457	snp	G/T	1.64738e-05	0.00286995	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47237968	GAAGATGATGTGTCA[G/T]CTCTATGACCCAGAA	1643
rs763214889	in-del	-/C	1.64742e-05	0.00286999	intron-variant	DDB2	GRCh38.p7	11:47232789	GCCCATCATCACTCA[-/C]TGGCTTTTTCCTTCC	1643
rs763232817	snp	C/T	0.000100231	0.0070785	intron-variant	DDB2	GRCh38.p7	11:47215311	GCCTTTTAGGGTGCT[C/T]GCGCAGGAGGCTGCA	1643
rs763308094	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47227658	TGGCACCCACCACCA[C/T]GCCCAGCTGGCCCGA	1643
rs763308575	snp	A/G	6.63735e-05	0.00576041	synonymous-codon, intron-variant	DDB2	GRCh38.p7	11:47234909	CTTCCTCTACTCGCT[A/G]CCGCACAGGCATCCT	1643
rs763312773	snp	C/T	1.66029e-05	0.00288117	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	DDB2, ACP2	GRCh38.p7	11:47238856	CGGAAGTGAGAGACA[C/T]TAAAGAAGGTGTGGG	1643
rs763313431	snp	A/G	3.29451e-05	0.00405851	missense, intron-variant, nc-transcript-variant	DDB2	GRCh38.p7	11:47232932	AAGGCAACATTCTAC[A/G]AGTTTTTGCCAGCTC	1643
rs763404900	snp	G/T			intron-variant	DDB2	GRCh38.p7	11:47225023	CAGCTCACTGCAACC[G/T]CCACCTCCCAGGTTC	1643
rs763472939	snp	A/G	1.69847e-05	0.00291411	intron-variant	DDB2	GRCh38.p7	11:47216258	CGTGCCGAATGAAAC[A/G]AGGCTTCCTTTCGGG	1643
rs763589079	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47228000	CAAAAATTAGCTGGG[C/T]GTGGTGGCGCACTCC	1643
rs763605006	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47229446	GAGTGGAGAGAGGGA[A/G]GAGGGTGATTGTGCC	1643
rs763697095	snp	A/G	0.000125696	0.00792668	intron-variant	DDB2	GRCh38.p7	11:47238194	AATGGGTGAGTAGGA[A/G]GAGAATGTCTCTGAC	1643
rs763720169	snp	A/G	1.67094e-05	0.0028904	intron-variant	DDB2	GRCh38.p7	11:47216286	GGGGAATTCAGCAGA[A/G]AAACCTTTCGTGAGA	1643
rs763722415	snp	C/T	1.64749e-05	0.00287005	synonymous-codon, intron-variant, nc-transcript-variant	DDB2	GRCh38.p7	11:47235286	TTGTTTCAGTCCCGA[C/T]GGAGCCCGGCTCCTG	1643
rs763784227	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47229057	TTTTCCCTTCCTGAA[C/T]AGTTCAAACCAAAAG	1643
rs763914353	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47218227	GAGATCTGATGCTTA[C/T]TTGTATGTTTGCCCA	1643
rs763969144	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47233823	GGTGTAACTAGCATT[A/G]GATTGGATCCTGGGC	1643
rs764157011	snp	G/T	1.64757e-05	0.00287012	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47237848	CTAGGCAGCCTGGCA[G/T]CCTCGCTACAACCTC	1643
rs764220947	in-del	-/CA	1.64832e-05	0.00287077	utr-variant-5-prime, nc-transcript-variant	DDB2	GRCh38.p7	11:47215108	GATCTTCGCATAGAG[-/CA]CACAGTACCCCTTCA	1643
rs764224665	snp	C/T	1.64953e-05	0.00287182	missense, intron-variant, nc-transcript-variant	DDB2	GRCh38.p7	11:47235353	GCTTCCCAGTGGGAC[C/T]GCCCCCTGGGCCTGA	1643
rs764369485	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47220754	GCCTCATTTTGTCAC[C/T]TCTTTAGTCATCTGA	1643
rs764538155	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47236434	TCTGCATTCTTTTCC[A/G]AAACTACAGATCCTC	1643
rs764542096	snp	C/G			upstream-variant-2KB	DDB2	GRCh38.p7	11:47213636	GCCTAGGCAACTTAG[C/G]GAGACTCTGTCTCTA	1643
rs764554542	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47237647	TCACCATGTTAGCCA[A/G]GATGGTCTCGATCTC	1643
rs764606058	snp	A/G	1.64762e-05	0.00287016	intron-variant	DDB2	GRCh38.p7	11:47234677	ACGGCAAAGAGGTGC[A/G]TTCTCCGAGGTCCTG	1643
rs764682019	snp	C/T	1.66255e-05	0.00288314	synonymous-codon, nc-transcript-variant	DDB2	GRCh38.p7	11:47216863	TCTGTGGCAGGGGCT[C/T]CAGCAGTCCTTTTTG	1643
rs764702738	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47238704	CGCCCGGCCTTCCTA[A/G]TATTTCTTTACCAAA	1643
rs764751185	snp	A/T			intron-variant	DDB2	GRCh38.p7	11:47229515	CGTGCATTTGGGGAG[A/T]GTGTGGCAGCAATAG	1643
rs764805641	snp	C/G	1.64732e-05	0.0028699	missense, intron-variant, nc-transcript-variant	DDB2	GRCh38.p7	11:47234634	GTCACAGGAGACAAC[C/G]TGGGGAACGTGATCC	1643
rs764937703	in-del	-/G			intron-variant	DDB2	GRCh38.p7	11:47225097	AGTGTGCACCACCAC[-/G]CCCAGCTAATTTTTG	1643
rs765161300	snp	C/T	1.65296e-05	0.00287481	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47216407	ATCCTGCCACCATGC[C/T]GCAGCATCGTCAGGA	1643
rs765214293	in-del	-/TATCTATC/TATCTATCTATCTATC			intron-variant	DDB2	GRCh38.p7	11:47228985	AAAGAAATATCTATC[-/TATCTATC/TATCTATCTATCTATC]TATCTATCTATCTAT	1643
rs765322033	snp	C/T	0.00668653	0.0574331	intron-variant	DDB2	GRCh38.p7	11:47229839	TTTTTTTTTTTTCTT[C/T]TTCCTAATAGAGACA	1643
rs765357628	snp	C/G	1.65392e-05	0.00287564	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47217028	TTTTGGCATCAAGGA[C/G]AAACCCACCTTCATC	1643
rs765406938	snp	A/G	1.64732e-05	0.0028699	synonymous-codon, nc-transcript-variant	DDB2	GRCh38.p7	11:47237944	CGACGTGTTCGATGG[A/G]AACTCAGGGAAGATG	1643
rs765459672	snp	A/G	1.64746e-05	0.00287002	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47237856	CCTGGCATCCTCGCT[A/G]CAACCTCATTGTTGT	1643
rs765513314	snp	C/T			synonymous-codon, downstream-variant-500B, nc-transcript-variant	DDB2, ACP2	GRCh38.p7	11:47238813	AGGTTACCACATTCT[C/T]ATCTGGAGCCAGGAG	1643
rs765551156	snp	A/G	1.64849e-05	0.00287092	intron-variant	DDB2	GRCh38.p7	11:47234741	GTCCCCACCTGAACC[A/G]AGCTCTTCTCTGCAG	1643
rs765557363	snp	A/G	1.6477e-05	0.00287024	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47215189	CCGAGATTGTATTAC[A/G]CCCCAGGAACAAGAG	1643
rs765583709	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47220926	GCACTTTGGGAGGCC[A/G]AGGCGGGTGGATCAC	1643
rs765788313	snp	A/G	1.65693e-05	0.00287826	intron-variant	DDB2	GRCh38.p7	11:47215282	CTGCCTGTGCCTGCT[A/G]CTTGAATATTTCCGC	1643
rs765800018	snp	A/G	3.29533e-05	0.00405901	intron-variant	DDB2	GRCh38.p7	11:47234687	GGTGCGTTCTCCGAG[A/G]TCCTGCCTTTCCCTC	1643
rs765910298	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47215568	ACCTTTCCTGGCGCT[A/G]TGTGTGCTGGATTTC	1643
rs765943148	snp	C/G			intron-variant	DDB2	GRCh38.p7	11:47235747	TGACCCACAAACCTT[C/G]ATTTTTTATTTTTTT	1643
rs765968563	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47220047	GCCCGCCTCGACCTC[C/T]CAAAGTGCTGGGATT	1643
rs765996055	snp	C/T			synonymous-codon, intron-variant	DDB2	GRCh38.p7	11:47234777	GAATCTCAGAATGCA[C/T]AAAAAGAAAGTGACG	1643
rs766169088	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47238027	GGTCCTCAAATAATG[A/G]TGGGAGGAAGCAGGG	1643
rs766181715	snp	A/T	1.67424e-05	0.00289326	synonymous-codon, intron-variant, nc-transcript-variant	DDB2	GRCh38.p7	11:47235403	CTTCCAGCACCTCAC[A/T]CCCATCAAGGTGAGT	1643
rs766212086	snp	C/T			upstream-variant-2KB	DDB2	GRCh38.p7	11:47213952	TTTGGGAGGCAGAGG[C/T]AGGAGGATCACTTGA	1643
rs766244670	in-del	-/CTC	1.65135e-05	0.00287341	cds-indel, downstream-variant-500B, nc-transcript-variant	DDB2, ACP2	GRCh38.p7	11:47238815	TTACCACATTCTCAT[-/CTC]CTGGAGCCAGGAGGA	1643
rs766290961	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47230934	GAGACCAGCCTGACC[A/G]ACATGGTGAAACCTG	1643
rs766359606	snp	A/G	1.64781e-05	0.00287033	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47216969	CCAACTCACCCCAGC[A/G]CTGTGGCTGTGGGTT	1643
rs766464790	in-del	-/G			intron-variant	DDB2	GRCh38.p7	11:47236653	GTCAGTATACTTAAA[-/G]CACTTGGCCCCATGC	1643
rs766565245	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47228733	AGGCCGAGGCAGGCG[A/G]ATCACTTGAAGTCAG	1643
rs766586298	snp	C/G/T	6.64714e-05	0.00576472	synonymous-codon, nc-transcript-variant	DDB2	GRCh38.p7	11:47238173	GGGGGACACGCTGGC[C/G/T]TCTGCAATGGGTGAG	1643
rs766586386	snp	C/T	1.64743e-05	0.00287	intron-variant	DDB2	GRCh38.p7	11:47232782	CGGCCAGGCCCATCA[C/T]CACTCACTGGCTTTT	1643
rs766707323	snp	C/T	1.69395e-05	0.00291024	intron-variant	DDB2	GRCh38.p7	11:47216263	CGAATGAAACAAGGC[C/T]TCCTTTCGGGGAATT	1643
rs766756674	snp	C/G	3.34342e-05	0.00408852	intron-variant	DDB2	GRCh38.p7	11:47215312	CCTTTTAGGGTGCTC[C/G]CGCAGGAGGCTGCAG	1643
rs766864062	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47224133	GAGAAGTCTGCTACA[A/G]TCCTTATGTTCCTGT	1643
rs766905158	snp	A/G	3.46362e-05	0.00416136	intron-variant	DDB2	GRCh38.p7	11:47216211	CACACAGACATGGAA[A/G]GGCCGCAGGAGGTGA	1643
rs766922655	snp	C/T	1.64738e-05	0.00286995	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47237969	AAGATGATGTGTCAG[C/T]TCTATGACCCAGAAT	1643
rs767028563	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47226399	TCCTGGCTCAGCCTC[C/T]AGTAGCTGAGATTAT	1643
rs767131311	snp	C/G	1.66371e-05	0.00288414	missense, intron-variant	DDB2	GRCh38.p7	11:47234922	CTGCCGCACAGGCAT[C/G]CTGTCAACGCAGGTG	1643
rs767157750	snp	C/T	1.64836e-05	0.0028708	missense, intron-variant	DDB2	GRCh38.p7	11:47234800	AAGTGACGCATGTGG[C/T]CCTGAACCCATGCTG	1643
rs767210223	snp	C/T			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	DDB2, ACP2	GRCh38.p7	11:47239214	ATAAAACCATACCGA[C/T]TGAGCTTCTGCGTGG	1643
rs767269675	snp	A/G	0.000138995	0.00833536	intron-variant	DDB2	GRCh38.p7	11:47229787	TAATCTTTTATAAGT[A/G]TCTCACCCTATGCTT	1643
rs767324814	snp	A/G	3.2963e-05	0.00405961	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47216972	ACTCACCCCAGCACT[A/G]TGGCTGTGGGTTCCA	1643
rs767371304	in-del	-/CTC	6.87817e-05	0.00586397	intron-variant	DDB2	GRCh38.p7	11:47238108	TAATACCTTCACCCT[-/CTC]CTCATGTTGACACTC	1643
rs767415233	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47215807	CTATAGTGATTGGGT[C/T]CTCAAATACAGTTTG	1643
rs767449553	in-del	-/A			intron-variant	DDB2	GRCh38.p7	11:47223235	TACGCCTGTAATCCC[-/A]GCATTTTGGGGGGCC	1643
rs767450571	in-del	-/GCC	1.73138e-05	0.00294221	intron-variant	DDB2	GRCh38.p7	11:47216212	CACAGACATGGAAAG[-/GCC]GCCGCAGGAGGTGAT	1643
rs767605781	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47220537	CACCTTATGACATGC[A/G]TGTAACCTTCTTTAC	1643
rs767689010	snp	G/T			intron-variant	DDB2	GRCh38.p7	11:47225581	TGGGCAACAGAGCGA[G/T]ACTCCATCTCTATTT	1643
rs767767775	snp	A/G	2.31801e-05	0.00340434	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47238180	ACGCTGGCCTCTGCA[A/G]TGGGTGAGTAGGAGG	1643
rs767854150	snp	A/C	1.64727e-05	0.00286986	missense, intron-variant, nc-transcript-variant	DDB2	GRCh38.p7	11:47232953	TTGCCAGCTCAGACA[A/C]CATCAAGTGAGTAGT	1643
rs768011030	snp	C/T	1.65004e-05	0.00287227	intron-variant	DDB2	GRCh38.p7	11:47238792	CAGACTGGTCTCACT[C/T]TTCCTAGGTTACCAC	1643
rs768184938	snp	C/T	1.65132e-05	0.00287339	missense, intron-variant, nc-transcript-variant	DDB2	GRCh38.p7	11:47235366	ACTGCCCCCTGGGCC[C/T]GATCCCGCACCCTCA	1643
rs768290979	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47221507	TGGAGTGCAGTAGCA[C/T]GATCTCGGCCCACTG	1643
rs768311836	snp	A/G	1.6473e-05	0.00286988	intron-variant	DDB2	GRCh38.p7	11:47234530	TGAGTAAATAGGACT[A/G]TCTCTGTCCCCAAGA	1643
rs768391561	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47220239	CAGTCAGAGGAGTGC[C/T]GCGGACAGAGTGGGG	1643
rs768530307	snp	A/G	1.64727e-05	0.00286986	missense, intron-variant, nc-transcript-variant	DDB2	GRCh38.p7	11:47232919	CTGCAAGACTTTAAA[A/G]GCAACATTCTACGAG	1643
rs768598903	snp	C/T	0.000162569	0.00901431	intron-variant	DDB2	GRCh38.p7	11:47238229	CAAGTCCGATCCTAC[C/T]TCCCAAGGTTCAGTG	1643
rs768651518	snp	C/T	3.29701e-05	0.00406005	intron-variant	DDB2	GRCh38.p7	11:47234729	CCTCGGTTCTGTGTC[C/T]CCACCTGAACCGAGC	1643
rs768662051	snp	C/G			upstream-variant-2KB	DDB2	GRCh38.p7	11:47214590	GACCCCGTCTCTCCA[C/G]AAAAAGAAAAAAAGA	1643
rs768717195	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47217837	CGAAGGTTGCAGTGA[A/G]CCGAAATCACGCCAC	1643
rs768815758	in-del	-/C			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	DDB2, ACP2	GRCh38.p7	11:47239158	TGGTAGCAGAGGGAT[-/C]CAAGCAGTTATTTGA	1643
rs768830995	in-del	-/T			intron-variant	DDB2	GRCh38.p7	11:47227470	ACTTCATAGATTGCC[-/T]TTTCACTTTGTCGAT	1643
rs768834799	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47225897	AGGCTTATTTCACTT[A/G]ATGCAGTGTTTTAAG	1643
rs768838299	in-del	-/AC	1.6473e-05	0.00286988	intron-variant	DDB2	GRCh38.p7	11:47234554	CCCAAGAATCTTACA[-/AC]ACAGTCTCTCCCTCC	1643
rs768902161	in-del	-/AAAT			intron-variant	DDB2	GRCh38.p7	11:47221215	AGAGAAAAGTGTAAA[-/AAAT]AAATTAAATATGATC	1643
rs768950337	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47238732	AAATTGTAGGTTTGC[A/G]GGCCAGCCCCAGGCT	1643
rs768981688	snp	A/G			utr-variant-5-prime, nc-transcript-variant	DDB2	GRCh38.p7	11:47215072	TTGTTTCTCCCCAGA[A/G]GCCTCTCAATCCTCC	1643
rs768992147	snp	A/G	1.71305e-05	0.00292659	intron-variant	DDB2	GRCh38.p7	11:47216244	AGACAGAGATTAACC[A/G]TGCCGAATGAAACAA	1643
rs769000976	snp	C/G			intron-variant	DDB2	GRCh38.p7	11:47230740	AGGTCTGTGAGGCTG[C/G]GATAGCTGCAGCGTA	1643
rs769079489	snp	A/C			intron-variant	DDB2	GRCh38.p7	11:47216048	AGAGTTCTGCATTGT[A/C]CTTTATCCTTGTGTG	1643
rs769110911	snp	A/C			intron-variant	DDB2	GRCh38.p7	11:47229900	CAGTGGCAGGATCAT[A/C]GCTAACTACAGCCTT	1643
rs769144378	snp	C/T	1.64827e-05	0.00287073	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47216946	GGGCTACATCCTTGG[C/T]GTGGCACCCAACTCA	1643
rs769162543	snp	G/T	3.29457e-05	0.00405854	synonymous-codon, nc-transcript-variant	DDB2	GRCh38.p7	11:47237911	CAAAAGTTGTACCCC[G/T]TATGAATTGAGGACG	1643
rs769319317	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47230858	GGGCGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC	1643
rs769321481	snp	C/T	3.29582e-05	0.00405931	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47216958	TGGCGTGGCACCCAA[C/T]TCACCCCAGCACTGT	1643
rs769399278	snp	A/G	3.4709e-05	0.00416573	intron-variant	DDB2	GRCh38.p7	11:47217084	AGGTCGTGCTAAAGA[A/G]GTGTTTGTTGGCTGG	1643
rs769400592	in-del	-/ACTT			intron-variant	DDB2	GRCh38.p7	11:47226951	TCTCTTACAGAAAGG[-/ACTT]ACTAAGTTAAAAAAA	1643
rs769425973	snp	A/T	1.64811e-05	0.00287059	utr-variant-5-prime, nc-transcript-variant	DDB2	GRCh38.p7	11:47215115	CGCATAGAGCACAGT[A/T]CCCCTTCACACGGAG	1643
rs769558893	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47238548	GGACTACAGGTGCCC[A/G]CTACCACGCCCAGCT	1643
rs769864556	snp	A/G	5.12492e-05	0.00506182	intron-variant	DDB2	GRCh38.p7	11:47216249	GAGATTAACCGTGCC[A/G]AATGAAACAAGGCTT	1643
rs769888365	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47234501	CTGTGGGTTAGTCAC[C/T]GGAGCGGCAACAGTG	1643
rs770064216	snp	A/C			intron-variant	DDB2	GRCh38.p7	11:47237421	TAGGTTGGCTTGTTA[A/C]TGGCAAATACTACTT	1643
rs770087391	snp	G/T	1.9214e-05	0.00309945	intron-variant	DDB2	GRCh38.p7	11:47238131	GTTGACACTCTTGTC[G/T]CTGCAGCTTAATGAA	1643
rs770236414	in-del	-/A			intron-variant	DDB2	GRCh38.p7	11:47219742	TTCTAGCTCTGGTTT[-/A]AAGGTAGACATGAGG	1643
rs770256505	in-del	-/C	0.000138246	0.00831286	intron-variant	DDB2	GRCh38.p7	11:47229826	GCTCTTCTTTTTTTT[-/C]TTTTTTTTTCTTCTT	1643
rs770341238	snp	C/G	1.65644e-05	0.00287783	missense, intron-variant	DDB2	GRCh38.p7	11:47234897	AGGGAAAGCCAGCTT[C/G]CTCTACTCGCTGCCG	1643
rs770358422	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47217941	GACCTCATCTTACGC[C/T]ATTGTCTTTTCTCAC	1643
rs770406867	snp	A/G	1.64727e-05	0.00286986	missense, intron-variant, nc-transcript-variant	DDB2	GRCh38.p7	11:47232859	AAGTTTAACCCTCTC[A/G]ATACCAACCAGTTTT	1643
rs770431096	snp	G/T	1.7795e-05	0.00298282	intron-variant	DDB2	GRCh38.p7	11:47217095	AAGAAGTGTTTGTTG[G/T]CTGGGTGCAGTGGTT	1643
rs770488181	snp	A/C			intron-variant	DDB2	GRCh38.p7	11:47226185	TTTTGAGGAACCGCT[A/C]TATTGTTTTCCATAC	1643
rs770543203	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47216785	TAGGGCTCATCCATG[A/G]AGGAGGCAGAGATTG	1643
rs770545184	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47233407	AAGAGAAAGTGGCTG[A/G]AGAAATTACAGAATG	1643
rs770622705	snp	C/G			intron-variant	DDB2	GRCh38.p7	11:47218091	AGGTCTTTGCTGATT[C/G]TACCTCTTCAAAGAG	1643
rs770839762	in-del	-/TCTTCTTTTTTTTTTTTTTTT			intron-variant	DDB2	GRCh38.p7	11:47229814	GCTTAATTTGATGGC[-/TCTTCTTTTTTTTTTTTTTTT]TCTTCTTCCTAATAG	1643
rs770855579	snp	A/G	1.6492e-05	0.00287154	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47215233	CTGGAGCTGGAGCCC[A/G]AGGCCAAGAAGCTCT	1643
rs770922074	snp	A/C/G	0.000165684	0.00910053	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47216462	GAGCTTCCTGGCCAT[A/C/G]TGTCCAGCAGGTAAG	1643
rs770993905	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47229268	AAGAGTAGAGGAGGC[C/T]GGGCATGGAATAGTG	1643
rs771013456	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47235515	GGTAAGCCTGCCACC[C/T]CAGATCGCTCCTGGC	1643
rs771105355	snp	G/T	1.64993e-05	0.00287218	intron-variant	DDB2	GRCh38.p7	11:47238769	GATTGGTAACAGAAA[G/T]TGTAAGTCAGACTGG	1643
rs771301538	snp	C/T			upstream-variant-2KB	DDB2	GRCh38.p7	11:47213144	CCGCTGGCTGCACGC[C/T]CTCTGGCCCATCACG	1643
rs771304920	snp	A/G	3.29478e-05	0.00405867	intron-variant	DDB2	GRCh38.p7	11:47235228	GCCAGGACCACAGAG[A/G]GCTTGTGGTTCCTTC	1643
rs771386513	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47227868	GATTTCTGGCCAGGC[A/G]TGGTGGATCACGCCT	1643
rs771533958	snp	A/G	1.65258e-05	0.00287448	synonymous-codon, nc-transcript-variant	DDB2	GRCh38.p7	11:47216346	GGCAGGTCCTAGCAG[A/G]AGATGTGACTCAGAC	1643
rs771681824	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47220131	TTGGAGAGCAGACCA[C/T]CAGAAAAGGCCAGGT	1643
rs771715652	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47235102	CCCATCAGCTGCTGA[A/G]TTTCCAGAATTTTTT	1643
rs771735781	snp	A/C	1.72311e-05	0.00293518	intron-variant	DDB2	GRCh38.p7	11:47238113	CCTTCACCCTCTCCT[A/C]ATGTTGACACTCTTG	1643
rs771793762	snp	C/T	1.64735e-05	0.00286993	intron-variant	DDB2	GRCh38.p7	11:47235248	GTGGTTCCTTCAGCT[C/T]AGGGGCTTTTCACTT	1643
rs771808474	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47218175	TCCCTGTATCATTAC[C/T]CTGCTTCATGTTTCC	1643
rs771890823	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47237551	TTCCCCTGCCTCAGC[C/T]TCCCAAGTAGCTGGG	1643
rs771894738	in-del	-/T			intron-variant	DDB2	GRCh38.p7	11:47221277	TGCATGTGTACACTA[-/T]TTTTTTTTTTTTCCA	1643
rs772015549	snp	A/G	3.29484e-05	0.00405871	missense, intron-variant, nc-transcript-variant	DDB2	GRCh38.p7	11:47234665	TGCTGAACATGGACG[A/G]CAAAGAGGTGCGTTC	1643
rs772017619	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47237279	TTAGGAAATGCAAAT[A/G]AGGGAGAAGGCCTGA	1643
rs772355051	snp	C/T	1.65247e-05	0.00287438	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47216366	GTGACTCAGACTGCC[C/T]CTGGGTGGGGCTGGC	1643
rs772394769	snp	C/G			intron-variant	DDB2	GRCh38.p7	11:47229334	GGAGGCCTAGAGTGG[C/G]GTGGCGGAGTCAAGT	1643
rs772461740	snp	C/T	3.32723e-05	0.00407861	intron-variant	DDB2	GRCh38.p7	11:47216489	TAAGGCATTTTTTGC[C/T]TCAAGTCCTCAAGGG	1643
rs772481534	snp	A/G			utr-variant-5-prime, nc-transcript-variant	DDB2	GRCh38.p7	11:47215123	GCACAGTACCCCTTC[A/G]CACGGAGGACGCGAT	1643
rs772492193	in-del	-/C			upstream-variant-2KB	DDB2	GRCh38.p7	11:47214908	TTGGCACCACCCCCT[-/C]CCCGCGCCCCCGCCT	1643
rs772542105	snp	A/G			missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47215257	AAGCTCTGTGCGAAG[A/G]GCTCCGGTACTGCCT	1643
rs772543255	snp	A/G			upstream-variant-2KB	DDB2	GRCh38.p7	11:47213229	GCAGTGAGAGGCCAA[A/G]AGGCTGGGCATGGTG	1643
rs772637982	snp	A/C	1.64784e-05	0.00287035	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47216962	GTGGCACCCAACTCA[A/C]CCCAGCACTGTGGCT	1643
rs772657169	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47230270	GCACCACTGCATCAA[A/G]GTTTTGAACTCCTGG	1643
rs772747534	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47219770	AGGGGGAACCCAGGA[A/G]GAGGTCTCTTTATTT	1643
rs772790115	snp	C/G			intron-variant	DDB2	GRCh38.p7	11:47232293	AGGTTGCAGTGAGCC[C/G]AGGTCGTGACAGAGC	1643
rs772811674	snp	G/T			intron-variant	DDB2	GRCh38.p7	11:47230894	GGGAAGCCGAGGCAG[G/T]CCAATCACCTGAGGT	1643
rs772949340	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47237677	CCTGACCTCGTGATC[C/T]GCCTGCCTCAGCCTC	1643
rs773516404	snp	C/G	1.65051e-05	0.00287267	intron-variant	DDB2	GRCh38.p7	11:47238752	AGCCCCAGGCTCTGA[C/G]AGATTGGTAACAGAA	1643
rs773567904	snp	C/T	1.92602e-05	0.00310318	intron-variant	DDB2	GRCh38.p7	11:47238132	TTGACACTCTTGTCT[C/T]TGCAGCTTAATGAAT	1643
rs773602928	snp	A/C	1.65809e-05	0.00287926	stop-gained, intron-variant	DDB2	GRCh38.p7	11:47234905	CCAGCTTCCTCTACT[A/C]GCTGCCGCACAGGCA	1643
rs773628645	snp	A/G	6.59391e-05	0.00574153	intron-variant	DDB2	GRCh38.p7	11:47234753	ACCGAGCTCTTCTCT[A/G]CAGCTTTGGAATCTC	1643
rs773718543	snp	A/C	1.65718e-05	0.00287848	intron-variant	DDB2	GRCh38.p7	11:47215283	TGCCTGTGCCTGCTG[A/C]TTGAATATTTCCGCC	1643
rs773828524	snp	A/G	4.96701e-05	0.00498323	missense, downstream-variant-500B, nc-transcript-variant	DDB2, ACP2	GRCh38.p7	11:47238842	AGGAAGCCAGGACAC[A/G]GAAGTGAGAGACACT	1643
rs773923267	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47233905	ATAGACAAGGCTCCA[A/G]GCTACTCTTCCGCAA	1643
rs773939874	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47218151	TAGATCCCACTCCTC[C/T]ACCGTCATTCCCTGT	1643
rs774005293	snp	A/G	6.64011e-05	0.00576161	synonymous-codon, intron-variant	DDB2	GRCh38.p7	11:47234912	CCTCTACTCGCTGCC[A/G]CACAGGCATCCTGTC	1643
rs774010230	in-del	-/TTTTTTTTTTTTT			intron-variant	DDB2	GRCh38.p7	11:47226735	TTCAAGTCCTTTGCC[-/TTTTTTTTTTTTT]TTTTTTTTTTTTGAA	1643
rs774149328	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47235037	CAAACCTTTACCCCT[A/G]ATAGCGTCTGCCAAG	1643
rs774225296	snp	A/C	3.56837e-05	0.00422381	intron-variant	DDB2	GRCh38.p7	11:47217096	AGAAGTGTTTGTTGG[A/C]TGGGTGCAGTGGTTC	1643
rs774235977	snp	A/G			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	DDB2, ACP2	GRCh38.p7	11:47238862	TGAGAGACACTAAAG[A/G]AGGTGTGGGCCAGAC	1643
rs774277740	snp	C/T	1.6473e-05	0.00286988	synonymous-codon, nc-transcript-variant	DDB2	GRCh38.p7	11:47237929	TGAATTGAGGACGAT[C/T]GACGTGTTCGATGGA	1643
rs774423409	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47235622	TTTTCTGTCTCGCTG[A/G]TAAGATATTTTTCTG	1643
rs774449547	in-del	-/A	1.64837e-05	0.00287081	frameshift-variant, intron-variant	DDB2	GRCh38.p7	11:47234778	AATCTCAGAATGCAC[-/A]AAAAGAAAGTGACGC	1643
rs774493775	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47217847	AGTGAGCCGAAATCA[C/T]GCCACTGCACTCCAG	1643
rs774558233	snp	C/T	1.64988e-05	0.00287213	intron-variant	DDB2	GRCh38.p7	11:47238782	AAGTGTAAGTCAGAC[C/T]GGTCTCACTCTTCCT	1643
rs774675310	snp	A/C/G	6.58941e-05	0.00573964	missense, intron-variant, nc-transcript-variant	DDB2	GRCh38.p7	11:47234664	CTGCTGAACATGGAC[A/C/G]GCAAAGAGGTGCGTT	1643
rs774721002	in-del	-/AG			upstream-variant-2KB	DDB2	GRCh38.p7	11:47214605	GAAAAAGAAAAAAAG[-/AG]AGAGAGAGAGAGAAA	1643
rs774817566	snp	C/T	1.69095e-05	0.00290765	intron-variant	DDB2	GRCh38.p7	11:47216268	GAAACAAGGCTTCCT[C/T]TCGGGGAATTCAGCA	1643
rs775040916	snp	A/C			intron-variant	DDB2	GRCh38.p7	11:47220197	GATGGGTGTTCAAGG[A/C]ACAAGTGCCAGAAGC	1643
rs775218808	snp	A/C	0.00260117	0.0359697	intron-variant	DDB2	GRCh38.p7	11:47229792	TTTTATAAGTATCTC[A/C]CCCTATGCTTAATTT	1643
rs775237497	snp	C/T	1.64977e-05	0.00287203	synonymous-codon, intron-variant, nc-transcript-variant	DDB2	GRCh38.p7	11:47235355	TTCCCAGTGGGACTG[C/T]CCCCTGGGCCTGATC	1643
rs775289096	snp	C/G	1.64738e-05	0.00286995	intron-variant	DDB2	GRCh38.p7	11:47235265	GGGGCTTTTCACTTT[C/G]CCAGCTTGTTTCAGT	1643
rs775374184	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47218193	GCTTCATGTTTCCCC[C/T]AAGTGTTGATGGGTG	1643
rs775425167	snp	C/T	1.72092e-05	0.00293331	intron-variant	DDB2	GRCh38.p7	11:47238115	TTCACCCTCTCCTCA[C/T]GTTGACACTCTTGTC	1643
rs775515178	snp	A/G	1.64727e-05	0.00286986	missense, intron-variant, nc-transcript-variant	DDB2	GRCh38.p7	11:47232886	TTTTACGCCTCCTCA[A/G]TGGAGGGAACAACTA	1643
rs775572160	snp	A/T			intron-variant	DDB2	GRCh38.p7	11:47222234	TTTACATTTTCTAGA[A/T]CTATATATAAATAGA	1643
rs775591023	snp	G/T	1.64874e-05	0.00287113	intron-variant	DDB2	GRCh38.p7	11:47234726	CCACCTCGGTTCTGT[G/T]TCCCCACCTGAACCG	1643
rs775705405	snp	A/G	6.58935e-05	0.00573955	missense, intron-variant, nc-transcript-variant	DDB2	GRCh38.p7	11:47234671	ACATGGACGGCAAAG[A/G]GGTGCGTTCTCCGAG	1643
rs775744305	snp	C/G			intron-variant	DDB2	GRCh38.p7	11:47227409	ACTGCGCCCGGCCAT[C/G]ATATTAACCTCTTAT	1643
rs775814662	snp	A/G	1.64977e-05	0.00287203	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47215239	CTGGAGCCCGAGGCC[A/G]AGAAGCTCTGTGCGA	1643
rs775823150	in-del	-/C	0.000146811	0.00856643	intron-variant	DDB2	GRCh38.p7	11:47229835	TTTTTTTTTTTTTTT[-/C]CTTCTTCCTAATAGA	1643
rs775893524	snp	A/C	1.65021e-05	0.00287241	splice-acceptor-variant	DDB2	GRCh38.p7	11:47238798	GGTCTCACTCTTCCT[A/C]GGTTACCACATTCTC	1643
rs776041354	snp	G/T	1.66779e-05	0.00288768	intron-variant	DDB2	GRCh38.p7	11:47216504	CTCAAGTCCTCAAGG[G/T]TTTACACGTGCATTT	1643
rs776043891	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47229385	ATGGAGAGGGGCGGC[C/T]GTGGCGCCTGATGTG	1643
rs776075728	snp	A/T	1.6517e-05	0.00287372	missense, intron-variant, nc-transcript-variant	DDB2	GRCh38.p7	11:47235368	TGCCCCCTGGGCCTG[A/T]TCCCGCACCCTCACC	1643
rs776207791	in-del	-/T			intron-variant	DDB2	GRCh38.p7	11:47227506	CTTTTGATGCCTGAA[-/T]TTTTTTTTTTTTTTT	1643
rs776224528	snp	C/G			intron-variant	DDB2	GRCh38.p7	11:47230773	GAAGAAGTGGAAAAG[C/G]TGGAGAAAGGCGGAC	1643
rs776325728	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47221588	TAGCTGGGATTACAG[A/G]AGCCTACCACCATGC	1643
rs776335108	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47224538	TACAGGCGTGAGCCA[C/T]CTTGCCCAGCCCATT	1643
rs776380322	snp	A/G	3.29641e-05	0.00405968	synonymous-codon, nc-transcript-variant	DDB2	GRCh38.p7	11:47216947	GGCTACATCCTTGGC[A/G]TGGCACCCAACTCAC	1643
rs776431970	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47220241	GTCAGAGGAGTGCCG[C/T]GGACAGAGTGGGGTA	1643
rs776525021	snp	A/G	1.6473e-05	0.00286988	intron-variant	DDB2	GRCh38.p7	11:47234551	GTCCCCAAGAATCTT[A/G]CAACACAGTCTCTCC	1643
rs776612511	snp	C/T	3.295e-05	0.00405881	missense, intron-variant, nc-transcript-variant	DDB2	GRCh38.p7	11:47235293	AGTCCCGATGGAGCC[C/T]GGCTCCTGACCACGG	1643
rs776815495	snp	A/G	1.65373e-05	0.00287548	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47215258	AGCTCTGTGCGAAGG[A/G]CTCCGGTACTGCCTG	1643
rs776994400	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47220815	CCTTGGCAAGGGAAC[A/G]TGTATTACAGTTTCA	1643
rs777078182	snp	C/G	0.000115391	0.00759487	intron-variant	DDB2	GRCh38.p7	11:47234731	TCGGTTCTGTGTCCC[C/G]ACCTGAACCGAGCTC	1643
rs777129573	snp	C/T	8.23784e-05	0.00641735	intron-variant	DDB2	GRCh38.p7	11:47234681	CAAAGAGGTGCGTTC[C/T]CCGAGGTCCTGCCTT	1643
rs777159854	snp	A/T			utr-variant-5-prime, nc-transcript-variant	DDB2	GRCh38.p7	11:47215081	CCCAGAGGCCTCTCA[A/T]TCCTCCCTCCATGAT	1643
rs777251885	snp	A/C	1.64901e-05	0.00287137	intron-variant	DDB2	GRCh38.p7	11:47238019	GAGGCTTGGGTCCTC[A/C]AATAATGATGGGAGG	1643
rs777303306	snp	C/G	1.6473e-05	0.00286988	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47237915	AGTTGTACCCCTTAT[C/G]AATTGAGGACGATCG	1643
rs777371027	snp	A/T			downstream-variant-500B	DDB2, ACP2	GRCh38.p7	11:47239271	AGCTTCTTGCGTCTC[A/T]GAAATGAAGAAAAAG	1643
rs777457500	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47233265	AGAAAGCCACCTAGA[A/G]AATGGAGCAACAGCT	1643
rs777698820	snp	C/T	1.64849e-05	0.00287092	synonymous-codon, nc-transcript-variant	DDB2	GRCh38.p7	11:47215217	GAGGAGCAGGAGTCC[C/T]CTGGAGCTGGAGCCC	1643
rs777699992	snp	A/C			intron-variant	DDB2	GRCh38.p7	11:47226035	ACTTGGGTTGATTTC[A/C]TCTTTTGGCTATTGT	1643
rs777763167	snp	C/T	1.64857e-05	0.00287099	synonymous-codon, intron-variant, nc-transcript-variant	DDB2	GRCh38.p7	11:47235334	CGAGATCCGAGTTTA[C/T]TCTGCTTCCCAGTGG	1643
rs777786685	snp	A/G	8.65569e-05	0.00657806	intron-variant	DDB2	GRCh38.p7	11:47216216	AGACATGGAAAGGCC[A/G]CAGGAGGTGATGAGA	1643
rs777793427	snp	C/T			upstream-variant-2KB	DDB2	GRCh38.p7	11:47213684	AGCTGAGTGTTGCGG[C/T]GCGCACCTGTAGTCC	1643
rs777808727	snp	A/C			intron-variant	DDB2	GRCh38.p7	11:47238562	CGCTACCACGCCCAG[A/C]TAATTTTTTGTATTT	1643
rs777810159	in-del	-/A			intron-variant	DDB2	GRCh38.p7	11:47218743	CAGAAGCCAGAGTGG[-/A]AAAAAAAAAAAAAAG	1643
rs777824005	snp	A/G	1.65356e-05	0.00287533	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47216432	TCAGGACCCTCCACC[A/G]GCATAAGCTGGGCAG	1643
rs777879172	snp	C/T	1.65326e-05	0.00287507	intron-variant	DDB2	GRCh38.p7	11:47216333	GTCTGTTCTGCTTGG[C/T]AGGTCCTAGCAGAAG	1643
rs777897561	snp	C/G			intron-variant	DDB2	GRCh38.p7	11:47216813	TTGGCAGTTTACCCA[C/G]AACTTGGGTTTTAAT	1643
rs777915636	snp	A/T			intron-variant	DDB2	GRCh38.p7	11:47230243	AGGTTGGGGCTACGC[A/T]GAGCCAGGATTGCAC	1643
rs778007189	snp	C/T			upstream-variant-2KB	DDB2	GRCh38.p7	11:47213069	AGGACAGCGCGGCCT[C/T]ACCTGTGAACCTTCA	1643
rs778193127	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47217958	TTGTCTTTTCTCACT[C/T]CTATGCTGTAGCCAC	1643
rs778196026	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47219194	GTGATCTGCCTGCCT[C/T]GGCCTCCCAAAGTGC	1643
rs778251026	snp	A/G	3.29478e-05	0.00405867	intron-variant	DDB2	GRCh38.p7	11:47232987	ACTAGCAGGGGAAAG[A/G]GCTTCTAAGCTTAGG	1643
rs778315100	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47238620	AGCCAGGATGGTCTC[A/G]GTCTCCTGACCTCGT	1643
rs778384866	snp	A/C	1.64741e-05	0.00286998	intron-variant	DDB2	GRCh38.p7	11:47233006	TCTAAGCTTAGGTGT[A/C]GTTCCGGCAAGAGCA	1643
rs778435738	snp	A/C/G	3.29453e-05	0.00405854	missense, intron-variant, nc-transcript-variant	DDB2	GRCh38.p7	11:47232865	AACCCTCTCAATACC[A/C/G]ACCAGTTTTACGCCT	1643
rs778504979	snp	C/T	4.99871e-05	0.0049991	synonymous-codon, intron-variant	DDB2	GRCh38.p7	11:47234930	CAGGCATCCTGTCAA[C/T]GCAGGTGTGATATCC	1643
rs778571431	snp	C/T	1.66515e-05	0.00288539	intron-variant	DDB2	GRCh38.p7	11:47216295	AGCAGAAAAACCTTT[C/T]GTGAGATTGGAGAGG	1643
rs778596999	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47219604	ATCCTTCTGTCTTGT[C/T]TTCCCAAATTGCTCG	1643
rs778597058	snp	A/C			intron-variant	DDB2	GRCh38.p7	11:47236547	CCCCCGGGTTAGAAT[A/C]CTTGGGCAAATTACT	1643
rs778626626	snp	A/C	5.0358e-05	0.00501761	intron-variant	DDB2	GRCh38.p7	11:47234954	GATATCCCAGACCTC[A/C]TCTCTCCTGCAGACC	1643
rs778641857	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47236244	GGCAACTTTGCCTTC[C/T]TAGTTTGTCTTGCAG	1643
rs778775117	snp	C/T	1.65321e-05	0.00287502	intron-variant	DDB2	GRCh38.p7	11:47238049	GAAGCAGGGATTCAA[C/T]CTACCTTATTGACCA	1643
rs778821228	snp	A/G	3.43059e-05	0.00414147	intron-variant	DDB2	GRCh38.p7	11:47216241	ATGAGACAGAGATTA[A/G]CCGTGCCGAATGAAA	1643
rs778882874	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47225872	CATACAGTATTTGTC[C/T]TTTTGTGACAGGCTT	1643
rs778949797	snp	C/G			intron-variant	DDB2	GRCh38.p7	11:47225763	ACCCACTGAACAAGC[C/G]TCCACTTCTCCCTCC	1643
rs778996174	snp	C/T			upstream-variant-2KB	DDB2	GRCh38.p7	11:47213492	CTCCGGCCTGGGCAA[C/T]AGAGTGAGACTCCGT	1643
rs779041734	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47230537	TGAGAACAACTACAA[C/T]CAACCCTTGGTTTGG	1643
rs779054085	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47215850	TGTTGCTTTATTGCT[A/G]TTCTAATTTCACTTA	1643
rs779437267	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47223378	TAATCCCAGCTACCC[A/G]GGAGGCTGAGGCATG	1643
rs779489467	snp	C/T	1.64893e-05	0.0028713	missense, intron-variant, nc-transcript-variant	DDB2	GRCh38.p7	11:47235342	GAGTTTACTCTGCTT[C/T]CCAGTGGGACTGCCC	1643
rs779578232	in-del	-/T/TT	0.00266365	0.036408	intron-variant	DDB2	GRCh38.p7	11:47229815	TTAATTTGATGGCTC[-/T/TT]TTCTTTTTTTTTTTT	1643
rs779609607	snp	G/T			intron-variant	DDB2	GRCh38.p7	11:47221134	TGCCACTGCACTCCA[G/T]CCTGGGCGACACAGT	1643
rs779621308	snp	A/C	1.6477e-05	0.00287024	synonymous-codon, nc-transcript-variant	DDB2	GRCh38.p7	11:47215193	GATTGTATTACGCCC[A/C]AGGAACAAGAGGAGC	1643
rs779659936	snp	A/C	1.64735e-05	0.00286993	missense, intron-variant, nc-transcript-variant	DDB2	GRCh38.p7	11:47234658	GTGATCCTGCTGAAC[A/C]TGGACGGCAAAGAGG	1643
rs779711588	snp	C/T			upstream-variant-2KB	DDB2	GRCh38.p7	11:47212953	AGGCACGGGGCTTAG[C/T]GGGTGGAGGAAAGGC	1643
rs779731799	snp	A/G	3.30644e-05	0.00406585	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47216416	CCATGCCGCAGCATC[A/G]TCAGGACCCTCCACC	1643
rs779794699	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47236713	CAATAAATGATGATT[A/G]AATATTGAGTGGCCC	1643
rs779817938	snp	C/T	6.58903e-05	0.00573941	intron-variant	DDB2	GRCh38.p7	11:47234523	GCAACAGTGAGTAAA[C/T]AGGACTATCTCTGTC	1643
rs779872957	snp	A/G	3.50576e-05	0.00418659	intron-variant	DDB2	GRCh38.p7	11:47238221	TGACTTGCCAAGTCC[A/G]ATCCTACTTCCCAAG	1643
rs780005436	snp	A/G	1.69137e-05	0.00290802	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	DDB2, ACP2	GRCh38.p7	11:47238900	TGGAGCCCACACATG[A/G]GATCAAGTCCTGCAA	1643
rs780099821	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47217740	ACTAAAGATACAAAA[A/G]ATTAGCTGGATGTGG	1643
rs780192669	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47229074	GTTCAAACCAAAAGT[C/T]ATTAGGTAGGATCAA	1643
rs780286263	snp	A/G	1.65004e-05	0.00287227	synonymous-codon, intron-variant	DDB2	GRCh38.p7	11:47234852	CTCCGTAGATCAAAC[A/G]GTGAAAATTTGGGAC	1643
rs780299180	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47215873	TTCACTTACCTCCCC[A/G]GAAGTAACCTAGTTA	1643
rs780332968	in-del	-/T			intron-variant	DDB2	GRCh38.p7	11:47227274	ACCATGCCCGGCTAA[-/T]TTTTGTGCTTTTAGT	1643
rs780555193	snp	C/T	1.64944e-05	0.00287175	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47216922	AAAAGGCTGCCCCCT[C/T]TGACAGGAGGGCTAC	1643
rs780557154	snp	G/T	3.29468e-05	0.00405861	synonymous-codon, nc-transcript-variant	DDB2	GRCh38.p7	11:47237872	CAACCTCATTGTTGT[G/T]GGCCGATACCCAGAT	1643
rs780665825	snp	C/T	3.29457e-05	0.00405854	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47237883	TTGTGGGCCGATACC[C/T]AGATCCTAATTTCAA	1643
rs780776638	snp	A/G/T	3.29664e-05	0.00405984	missense, nc-transcript-variant	DDB2	GRCh38.p7	11:47215213	ACAAGAGGAGCAGGA[A/G/T]TCCCCTGGAGCTGGA	1643
rs780921271	snp	G/T	1.64832e-05	0.00287077	utr-variant-5-prime, nc-transcript-variant	DDB2	GRCh38.p7	11:47215108	TGATCTTCGCATAGA[G/T]CACAGTACCCCTTCA	1643
rs781117402	snp	A/G	1.64738e-05	0.00286995	missense, intron-variant, nc-transcript-variant	DDB2	GRCh38.p7	11:47234661	ATCCTGCTGAACATG[A/G]ACGGCAAAGAGGTGC	1643
rs781207574	snp	C/T	8.24056e-05	0.00641841	intron-variant	DDB2	GRCh38.p7	11:47234698	CGAGGTCCTGCCTTT[C/T]CCTCCCTCACCCCCA	1643
rs781227843	snp	A/G			upstream-variant-2KB	DDB2	GRCh38.p7	11:47214475	CCCGGACCCGCAGAG[A/G]CCTGGCAGCGCCGCG	1643
rs781231692	snp	A/C	1.6886e-05	0.00290564	intron-variant	DDB2	GRCh38.p7	11:47234968	CATCTCTCCTGCAGA[A/C]CCTGCCTGTCTGACC	1643
rs781240281	in-del	-/T			intron-variant	DDB2	GRCh38.p7	11:47238403	GTTTCCTAGTATTTC[-/T]TTTTTTTTTTTTGAG	1643
rs781286785	snp	A/G	1.65282e-05	0.00287469	missense, intron-variant	DDB2	GRCh38.p7	11:47234880	GACCTGCGCCAGGTT[A/G]GAGGGAAAGCCAGCT	1643
rs781343259	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47218975	TTTGAGGCGGACTCT[C/T]GCTCTGTCACCCAGG	1643
rs781389544	in-del	-/A			upstream-variant-2KB	DDB2	GRCh38.p7	11:47214772	CCAGACCCTGTTGCT[-/A]AAAAAAAAAAAAAAA	1643
rs781456290	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47227413	CGCCCGGCCATGATA[C/T]TAACCTCTTATCAGA	1643
rs781493486	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47222526	TTTTAAAATTTTGTT[A/G]TAGAGACAGAGGTCT	1643
rs781545215	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47217899	CCATCTCAAAAAAAA[A/G]GAATTGAAGCCCCTT	1643
rs781592890	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47231936	TTGCAAATGTTCTGC[A/G]TCCTGATTTGGGTGG	1643
rs781613674	in-del	-/A			intron-variant	DDB2	GRCh38.p7	11:47233711	CGAAAATCTATCTCA[-/A]AAAAAAAAAAAAAAA	1643
rs781655324	snp	A/C	1.64795e-05	0.00287045	stop-gained, nc-transcript-variant	DDB2	GRCh38.p7	11:47238000	CTTCTGGCATCAGTT[A/C]GGTGAGGCTTGGGTC	1643
rs781686709	snp	C/T	1.64735e-05	0.00286993	intron-variant	DDB2	GRCh38.p7	11:47232799	ACTCACTGGCTTTTT[C/T]CTTCCTCGTGTTAGA	1643
rs781721341	snp	C/T	1.72009e-05	0.0029326	intron-variant	DDB2	GRCh38.p7	11:47217073	TTCCCCATGCCAGGT[C/T]GTGCTAAAGAAGTGT	1643
rs796440495	snp	C/T			intron-variant	DDB2	GRCh38.p7	11:47226838	CCTCGAACTTCTGGG[C/T]TCCAGTGATCCTGCT	1643
rs796892430	snp	A/G			intron-variant	DDB2	GRCh38.p7	11:47224461	CACCATGTTGGCCAG[A/G]CTGGTCTTGAACTCC	1643

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