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

HECTD2

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs185099954	snp	A/C	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502959	TTTCAATTTGACATA[A/C]TAATGGTATGCCTCA	143279
rs185134164	snp	C/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433415	TTTCCACCTTTGGTG[C/G]GTAACTATGTATGCA	143279
rs185152898	snp	G/T	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476444	ACGGACCCCCACGAA[G/T]TTTCTCCCTGATGGA	143279
rs185238186	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91413322	CTAAGACCATCTAAA[C/T]GTGAAGGAAGTCCAT	143279
rs185240177	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91436722	ATTTTTGCCTTCCCC[A/G]TTATATTCCCAGTTC	143279
rs185241826	snp	C/G	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431104	CCTCAGCATTTGCTT[C/G]TCTGTAAAGTATTTT	143279
rs185255509	snp	A/G	0.00517822	0.0506191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452055	AGGGGATAGGAATCA[A/G]TGAACTGGAAGACAG	143279
rs185263815	snp	A/G	0.00318978	0.0398085	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91472858	GAAGTAGAGAAATTA[A/G]TAGATTAAACAGCAG	143279
rs185298248	snp	C/T	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457762	AAGGATGTCTGCTCT[C/T]AGCACTCTTATTCAA	143279
rs185316940	snp	A/G	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503979	TGACACCTGACCCCC[A/G]AGCAGCCTAACTGGG	143279
rs185328664	snp	G/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487199	GATTTATTTTTATTG[G/T]TCTTAAATATATTAC	143279
rs185366815	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438255	ACTCACTGACAGGTC[C/T]TGGTGTGTGATGTTC	143279
rs185438597	snp	C/T	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460734	AAGAAAACAAATATA[C/T]AAATAACAGGAAGAG	143279
rs185488165	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439089	AGTTTAATTAGATGC[C/T]ATTTGTCAATTTTGG	143279
rs185490263	snp	G/T	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91418712	AAATATCTTTACCCA[G/T]GATCAAGGCCTAAAA	143279
rs185521721	snp	G/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91514188	TGTAAACAGTTTTTA[G/T]TTGGTAGAGATGACT	143279
rs185556769	snp	G/T	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91465542	TATCTCACCATTAAT[G/T]ATGATGTTAGCTGTA	143279
rs185565598	snp	C/T	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91488056	GAGCTTGTTGGACCT[C/T]GTTTTGCAGATACCA	143279
rs185699913	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491467	CTTCTGTAAAGTTTG[A/G]TACCATAGTTAAAAT	143279
rs185731485	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445907	GACAAGGAGATTCTC[C/T]TGGGTGCCTATGCCA	143279
rs185870242	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462364	TTTATTTTTTAATTA[C/T]GAATTAAGCAGCAAA	143279
rs185892923	snp	A/G	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419201	ACCAGAATTTTGAAT[A/G]TAGTACCACTTGTTA	143279
rs186003701	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91488856	CAAAGCCACACTACC[C/T]CCCTGAAGAATGAGT	143279
rs186006814	snp	C/T	0.0023933	0.0345097	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91424108	AAGAACCCAAGCTAA[C/T]AGATGCTCTAACATG	143279
rs186008956	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450397	GATTAAAAACTTAAA[C/T]GTAAAACCTAATACT	143279
rs186073916	snp	A/T	0.0182019	0.0936463	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468777	CTCTACAAAAAAAAA[A/T]TTTTTTAAGTTAGCT	143279
rs186076373	snp	A/T	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91495383	TTATTATCAGACTTC[A/T]TTACACCTTAGCAAA	143279
rs186113174	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449882	GAAATAAGAGAGAAC[A/G]CAAACAAATGGAAAA	143279
rs186125244	snp	A/G	0.00279162	0.0372561	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493044	ATGTGATGGGAAATA[A/G]GGATGACAGTGATAA	143279
rs186252968	snp	C/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467768	CAGTATGTGTGCGTA[C/G]CCCACCAGGCTACTG	143279
rs186254286	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452810	AATTTTTCAAATGCT[A/G]AAAGGACTGTCAATG	143279
rs186285249	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422732	GACTATTTTATGGAA[A/G]GGTATTGTGTATCAC	143279
rs186296543	snp	C/T	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91473571	ATGAGTTCACTCACA[C/T]ACAGATTTTATTCCG	143279
rs186302919	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499742	ACACTTTCATCATGC[C/T]ATTTATACCTCCCTT	143279
rs186401719	snp	A/T	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91474354	TCACTTTAGATTTTT[A/T]AAAATTATATTCCAT	143279
rs186464162	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432028	GTACTGAATTTTCCT[A/G]GCTGTTCTATCTGGA	143279
rs186499376	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91423297	GGGCATGGAAATTCA[A/G]TTTCCCCATCTATAA	143279
rs186504206	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450078	ATAGTCAAGACAATC[C/T]TAAGCAAAAAGAACA	143279
rs186574781	snp	G/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91408240	AAGAAATGGGTTATC[G/T]ACTCTGGTGCAGTAG	143279
rs186589837	snp	A/G	0.00636936	0.0560724	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432453	GTGAGAAGTGTAGGA[A/G]TTTTACCTACTGTAA	143279
rs186623421	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501082	TTACAGAAATTCAGG[A/G]TATTATGTATGCTTA	143279
rs186632330	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91454304	AAATTTTGAAGAATT[C/G]AGATAATGTAAAGTG	143279
rs186639720	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91475674	GAAGATGGCCCAAAC[A/G]AGATGTTTTAAATAA	143279
rs186648085	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502031	GAATCTGTTCTTTGC[C/T]TTTCCACTGCCTCTA	143279
rs186650082	snp	A/C	0.00279162	0.0372561	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91456966	GACAGAAAAAGGTAG[A/C]TTGTCAGTATGATAA	143279
rs186651257	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91407781	CTCAGGTCTTCCATC[A/T]GGACTTAGAAACATG	143279
rs186658845	snp	A/G	0.00438332	0.0466095	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91453945	GAGACAGAGGGGAAC[A/G]TTATATAATGATAAA	143279
rs186671044	snp	A/G	0.339882	0.233284	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503768	CTCGAACTGGGTGGA[A/G]CCCACCACAGCTCAA	143279
rs186677845	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412901	GTGTGAGGTAGGTGG[C/G]CAGGGAAATACAGCT	143279
rs186877594	snp	C/T	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478134	ACAGATCTGTAAATA[C/T]AATTAACATATAAAC	143279
rs186905963	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91436079	TATTCCTCTGAGAAA[C/G]CTAGTAATAAGTTTA	143279
rs186987847	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437728	TCAGTTTTTTATAAT[A/C]GATGACATATACATT	143279
rs186990083	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415833	TAGGATATCTATTTG[C/T]TTTTTTATGGTATGA	143279
rs187000512	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458921	CTCTGAGAAAGACCC[C/T]GTGCAGAGGATGAAA	143279
rs187058490	snp	A/C	0.00478085	0.0486577	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485431	ATATAGTTCAGATAG[A/C]CTTGAAATATCATAT	143279
rs187064423	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91511062	AACACTGAGTAAATG[C/T]TGATTCTAGTAGTTT	143279
rs187131336	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431718	GTTCTCGAGCCTTGG[C/T]TTTCAGCTCCATCAG	143279
rs187187943	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91435432	GGGACTTCATGACCC[C/T]GCTGGCAAGCCAGGA	143279
rs187232311	snp	A/C	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420629	GAAAATCAGTCTACT[A/C]TGCCTCCTTTTGGCA	143279
rs187238172	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444859	TTATCAGTGAAAATC[C/T]ATCATTTAGGGTTCA	143279
rs187238287	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91463779	AATAAAATTGTTTCA[A/G]AAACCTTACCAAATA	143279
rs187300101	snp	C/T	0.00279162	0.0372561	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91489832	AGTAGCCTTAAATTG[C/T]AGATTTGTGATACTA	143279
rs187312113	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468054	CAGCAGATGTGTGTG[C/T]ATCCCATCACATGGC	143279
rs187404689	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412353	GTACTACTAGACAAA[A/G]AGAAGAATATATTCA	143279
rs187448925	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91414942	TGAAACAGAGGAACA[A/G]CATAATGAAATCAGT	143279
rs187457499	snp	C/T	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493963	TCCATAAAAATTGAA[C/T]GGAATGGGAATATTT	143279
rs187552046	snp	A/G	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476165	TGATACAGGAGAGAT[A/G]AGGAAAAACTTTAAT	143279
rs187561737	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464998	TTTCCAAAACTCACT[A/T]AAAAATTTTCATACA	143279
rs187582380	snp	C/G/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421038	TTTGCATTCTTCCCC[C/G/T]CCTCAGGCTTTTTTC	143279
rs187624169	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502665	GTCCTAAAATGAAAA[A/C]ATTCAAGAGGATTTT	143279
rs187720679	snp	A/G	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91443701	GCCCCTTCCCCCAGG[A/G]AGAATTTGTATTTCT	143279
rs187798954	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496428	ATCATCTTTTTTCTA[C/T]CTGCACAGTCTCTCC	143279
rs187818828	snp	C/T	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425533	AAAAGAAGCTGTATA[C/T]GTATTTACCAGAAGC	143279
rs187826417	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481563	ACTATGTATTTTTCA[A/G]TAACTTCAATTAGAA	143279
rs187827472	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490527	CAGGTTTATCATCAG[A/G]AATATATACCTTGTT	143279
rs187855567	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445815	CTAGCCAAGGGAAGT[C/T]GTGAGAGACTGTGCC	143279
rs187882269	snp	A/C	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450990	CAGAAATACCATTTA[A/C]CCTAGCAATCCCGTT	143279
rs187892584	snp	C/G	0.00716266	0.059414	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470975	TCTGTGTGGCAGAGA[C/G]ACACACACACACACG	143279
rs188053894	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91446167	TCTGGGACAAAGCTT[C/T]CAGAGGAAGGAACAG	143279
rs188068248	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91469820	TATATGCTGTCTTCA[A/G]GAGACCCATCTCACA	143279
rs188094301	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91424765	ATTCTGGTATGCCCA[A/G]TCACAGTGCTTAGAA	143279
rs188122860	snp	A/C	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476758	CGAGAGGAGTGAGAA[A/C]CGTCTTCTTGAAGTT	143279
rs188243936	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91411682	TGTTAAAACAAGCTC[C/T]TTAAATCAATGCAGC	143279
rs188247891	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91435010	GGTATCATGGGGCAG[C/G]AACATTACTCTTAGC	143279
rs188252759	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91456249	GTCCTGTTTTATTTC[A/G]TTGAGCAGTGGTTTG	143279
rs188310874	snp	A/C	0.0134861	0.0810011	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476995	ACCATCCTGGCTAAC[A/C]AGGTGAAACCCCGTC	143279
rs188319168	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503592	AAAAACGGTGCACCA[C/T]GAGATTATATCCCGC	143279
rs188337655	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509229	TGTATACGTATGTAA[C/G]TAACCTGCACAATGT	143279
rs188366218	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503203	TGCAAATCAAAACCA[C/T]AATGAGATACCATCT	143279
rs188370254	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458540	TATTATATAGCTACA[A/G]TAATCATACTGAGAT	143279
rs188579236	snp	C/G	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91489453	CTAAAATAAGTTCCT[C/G]AGTCACAGTGTCAAG	143279
rs188589772	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91455130	TCTAGTTCGAGATCC[C/T]TGAGGAATCGCCACA	143279
rs188624610	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409467	AACAAGGAAGGGACG[C/G]ATAGGAGACAGCAAA	143279
rs188645610	snp	A/G	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437410	ACATCTCAAAAGAGA[A/G]AGCCAAGCACAAATG	143279
rs188645773	snp	C/T	0.00517822	0.0506191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449495	GACAGAAGACAAGGA[C/T]GCCCTCTCTTACTAC	143279
rs188652638	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91466872	AACCTTAAATACATA[C/T]TGCTAAGTGAAGGAA	143279
rs188658340	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483192	TAGAAATGATGCTTA[C/T]ATTCACAATGCTTCA	143279
rs188662839	snp	C/T	0.00318978	0.0398085	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492590	TTACAGACTTTTTGT[C/T]CATCGTAAATGTTGA	143279
rs188739717	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410972	CCTGCCTGCCTTGGA[A/G]GCGCGCAGATTTTTG	143279
rs188829872	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437029	CCCTTTGTTTCTTTA[A/G]CAGATAAGGAGTATG	143279
rs188892608	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451370	ACACTGGGGCCTTTC[A/G]GTGGATTGGGACCAG	143279
rs188895056	snp	A/T	0.00358779	0.0422022	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91418011	TTCCTATTTCTCCAC[A/T]TCCTCTCCAGCACCT	143279
rs188895749	snp	A/G			intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91463009	CCAATTGTGACTAAT[A/G]TATGGAAATACTTTC	143279
rs188899902	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432855	TGTGATCTTTGTCAC[C/T]CTGAAATAGCCAGGG	143279
rs188903023	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471513	GGCACCAAAATAGGA[C/T]GAGAGGAAGTCAAAT	143279
rs188911420	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438288	CTTTCTGTGTCCATG[G/T]GTTCTCATTGTTCAA	143279
rs188913388	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498366	CAGTCAATGAAAGTG[C/T]TTAATGAAATTCACT	143279
rs189111917	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457910	TACTCTTATTCATCT[C/T]AGTGCTGCAAATTTT	143279
rs189148068	snp	A/G	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421975	TCCTCTTCATTCCCT[A/G]TTATTACTATCTCTA	143279
rs189151746	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445962	AAACTGGGTGGCCAT[C/T]TGAGCAGACACCGAA	143279
rs189155112	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91413809	AGTGGTTCCAGTTAG[A/G]GATTCTCAAGAGGCT	143279
rs189198788	snp	C/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497567	GCCCACCTCGGCCTC[C/G]CAGAGTGCTGGGATT	143279
rs189210451	snp	A/C	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467788	CCAGGCTACTGCTGC[A/C]TGAGTACATGCTTGC	143279
rs189216093	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91466798	GGTACATTCCATATC[A/G]TGGAAATTATTCAGT	143279
rs189333208	snp	C/T	0.0271762	0.113356	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503654	CTCGCTGATGGCTAG[C/T]GCAGCAGTCTGAGAT	143279
rs189422481	snp	C/T	8.51738e-05	0.00652531	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498919	CTATAATTTAAAGCC[C/T]GGTGGTGATAAAATT	143279
rs189452757	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451903	GTAGAATTAAATTCT[A/G]TATATGTATATTTCA	143279
rs189457677	snp	C/T	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493138	CTTTTTATAAAGTTA[C/T]CTGATTCATTTAGTT	143279
rs189493320	snp	C/T	0.00358779	0.0422022	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450062	CCAAAAAAGAGCCCA[C/T]ATAGTCAAGACAATC	143279
rs189575271	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431414	TGTATTTCCTGAATC[A/T]GAATGTTGGCCTGCC	143279
rs189581101	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452202	AGGAGAGGAAAAGAC[A/C]GTAGGGCTAAAAAAG	143279
rs189586545	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91473070	TGGGGGTGTATATTT[A/G]ATACCTGGGAGTTTC	143279
rs189718322	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433455	ACCTTGCTTTTTGTC[A/C]AGTTCATGTATTCTA	143279
rs189722832	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457764	GGATGTCTGCTCTCA[A/G]CACTCTTATTCAACA	143279
rs189725166	snp	C/G	0.046775	0.145601	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91430850	TTTGCCAGTCTGTGT[C/G]TTTTAATTGGAGCAT	143279
rs189730911	snp	C/T	0.0105703	0.0719265	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481044	TTTTTCGTTAGATGC[C/T]ATGAGATTAAACATT	143279
rs189737331	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91504017	CTCCAGCAGGGGCAC[A/G]CTGACACCTCACACT	143279
rs189742172	snp	A/G	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91472503	GCAAAAGAAACTATC[A/G]ACACAGTAAGTAGAC	143279
rs189758262	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91436759	CTGTGCCCTTTAAGA[A/G]TTCTGCAGTATAAAT	143279
rs189760291	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91413507	AAAGCCATCATTATC[C/T]AGGCCCAAATGCAGT	143279
rs189960231	snp	C/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91408011	GGCAGTTGGGAATGT[C/G]TCTCTCAAGCACACC	143279
rs189964560	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440131	TTGAATAAGAGTAGT[A/G]AGAGAGAGCATCCTT	143279
rs189966431	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461635	CTCACTGCAACCTCT[A/G]CCTCCTGGGTTCATG	143279
rs189977057	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91488119	GAGAACTGCGGTGAG[A/G]CAGAGTGTCATTAGG	143279
rs189984603	snp	C/T	0.139903	0.224452	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91427006	CCCTCCCCCCTCCCC[C/T]CACCCCACAACAGTC	143279
rs189985891	snp	A/C/T	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91455787	GTTTTAGCTTTCTAC[A/C/T]TATGGCTAGCCAGTT	143279
rs189993824	snp	A/G	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422206	ATATGGCCACTACCT[A/G]CCTTCCCAGTCATAT	143279
rs190007922	snp	C/T	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419090	TGGAACAGCCAGCAC[C/T]TACTCCTTTTTTCAA	143279
rs190015254	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460859	CTGTTACCATTTTTA[G/T]AAATAAGAGTTCATT	143279
rs190034836	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91514841	TAAATGCAAGCTATT[C/G]TTTGCATTATACTCT	143279
rs190036313	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91513449	AAAATAAAATTCAAC[A/G]TTTTGGCCAAAATGT	143279
rs190206676	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91413116	ATAGTGGCTTTTTCA[G/T]AAAATCATTGTACCA	143279
rs190227100	snp	A/G	0.00478085	0.0486577	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91436476	TCTCTTGATTGGTCA[A/G]TCACTTAGTATTCAG	143279
rs190273384	snp	A/T	0.0551013	0.156571	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412630	TGATTATTTATTTTT[A/T]AAAAAAAAAAACAAT	143279
rs190278809	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487213	GGTCTTAAATATATT[A/G]CTTTACTTTTTACAT	143279
rs190279899	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91456758	TACGTCAAAAAGGGG[G/T]AAAGTTTCAAAACAA	143279
rs190398869	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91469594	TGCCTTACAAGAAAT[C/G]CTTAAGGGAGTACTA	143279
rs190406310	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91495410	CAAATTGAAATTTTG[A/G]TGGTCTTCCAATTTT	143279
rs190494054	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91486033	ACTAGCAAGACTATT[C/T]CAAACATAATTTATC	143279
rs190495263	snp	C/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477498	GAGCAGGGATACTCT[C/G]TGGGTGTGCGGGGTT	143279
rs190525452	snp	C/T	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438058	CCTTGAAGTTCTTTT[C/T]TGAAACCTTAGGAAC	143279
rs190527210	snp	C/T	0.00557542	0.0525036	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91435730	TGTGAGGTTTGTATT[C/T]ATCCCTTGTGCTATA	143279
rs190642026	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91473790	TAATACATAATACAT[A/G]TAAAATATGTGTTAA	143279
rs190645823	snp	A/G	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420543	CAGTGAGCCGAGATC[A/G]TGCCACTGCACTCCA	143279
rs190646114	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91443764	CTGCACAAAATACTA[C/T]GAAACACTCTTCCAT	143279
rs190650280	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499853	CTTTGGGGCAAAACC[A/C]AGTGGCTTACATTAT	143279
rs190658582	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91463452	GCACAATTCAAGCCT[G/T]TATTCAAGAGTCAAC	143279
rs190715200	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91489590	CATAAATTTGTTTAT[G/T]AGTTATTTCCAATGT	143279
rs190738662	snp	C/T	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91459690	AAGACTTACAGAGGA[C/T]GTAAGTGCATATACA	143279
rs190751799	snp	A/G	0.00279162	0.0372561	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91423066	ATTAAATTTAACTCA[A/G]CATACATCTATAAAA	143279
rs190753529	snp	A/G	0.0221141	0.102801	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512456	GCCTTTAGCCTTTTC[A/G]TGTTTCTGTCTCAAA	143279
rs190761665	snp	A/G	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91417286	GTGTGACATTCTAGT[A/G]AGCCATCAAAAAACA	143279
rs190885706	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91423583	GTTCCCATGTAGTGT[A/C]CATTACATCTCCATT	143279
rs190900163	snp	C/T	0.00279162	0.0372561	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450223	AGAAATAATGCCACA[C/T]ATCTACAGTAATCTG	143279
rs190908334	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468252	CCAGGGGCTCGGTAC[C/T]AGCACCCCCCAGAGT	143279
rs190959550	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493986	GAATATTTAAAGCAT[A/G]TAGTATTATTTTATA	143279
rs191058870	snp	C/T	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502395	AAAGCCAAAAGTCAT[C/T]ATGTATTGAGTTTCT	143279
rs191100098	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420684	ACATAGATTGGAAGC[A/G]GAAAGCAAAGGAACA	143279
rs191108199	snp	A/G	0.00279162	0.0372561	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91454143	AGAAAATCAACAAGT[A/G]TGTAGAATATAGAAT	143279
rs191122955	snp	A/C	0.0023933	0.0345097	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501461	AAAATCTTCAGAGTA[A/C]ACATGGCCTTGAAAT	143279
rs191290597	snp	A/G	0.00279162	0.0372561	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432193	CTCTCTTACTTGCCA[A/G]TAAGATTGTTTTTTC	143279
rs191355042	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91474538	GAGAAATCACTGGAA[C/T]TGGGAAGGTTATACA	143279
rs191367638	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478393	TATAATAACATAGAT[A/G]AGAAAAGAATTATAA	143279
rs191371841	snp	A/G	0.0023933	0.0345097	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450470	ATAGGCGTGGGCAAA[A/G]ACTTCACGGCTAAAA	143279
rs191481603	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485502	TGTACATGTTAATTT[G/T]GTTTTGGTTTGGTTA	143279
rs191491862	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91511110	GGGGCTCTCAAAATT[C/T]AGTTTTAAATCTTAC	143279
rs191517934	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437741	ATAGATGACATATAC[A/G]TTGTAAGTTTCCATA	143279
rs191525792	snp	C/G	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91459212	ATGACACCACCAAAT[C/G]CTGGTGAGTATGTAG	143279
rs191603208	snp	A/G	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457036	GAAAAAATAATAAGG[A/G]AATACTGCAAACTCT	143279
rs191607911	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91424274	ATCAGATGGCTCTAC[C/T]TAACTGCAAGAGAAT	143279
rs191613474	snp	C/T	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431896	TTCAAAGTCATTCTC[C/T]GTCCAGCTTTGTTCC	143279
rs191620090	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503915	GGGGTTCTCCTAGTA[C/T]GCAGCTGGAGATCTG	143279
rs191690811	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433719	AGATGTGGGGTTGTT[A/G]GGCCCAGGAGTAAAT	143279
rs191699002	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490041	TTTTAAATATATTGT[C/T]TTTTACCTATTCAGT	143279
rs191707952	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91456099	AAGTAGTTTTTTCCA[A/G]TTCTGTGAAGAAAGC	143279
rs191729015	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91411063	TCCACTTAATTGTGA[C/T]CTTTCCGTTGCTGTC	143279
rs191730320	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445639	GCAGCTCCCAGTGAG[A/G]TCAACGCAGAAGGCA	143279
rs191733424	snp	A/G	0.00279162	0.0372561	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464714	TGCTGACACAGCTAT[A/G]GTTGGAGCACACACC	143279
rs191847477	snp	A/G	0.00398564	0.0444627	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91413884	TGCTGCTGTGGAGAG[A/G]TGATGCAAATCCATG	143279
rs191884384	snp	C/T	0.140242	0.224618	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509122	CACTCTGGGGACTGT[C/T]GTGGGGTGGGGGGAG	143279
rs191910779	snp	A/C	0.256061	0.249927	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458037	CAAAAAAAAAAAAAA[A/C]CCCATGAAATCTCAA	143279
rs191911699	snp	G/T	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437527	CAAAGGGAGGCGAAT[G/T]AGACTCCATCCTTTG	143279
rs191916698	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458615	TGTAATTTGACAAAG[A/G]TCCAAAAGCAATTCA	143279
rs191923660	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91453165	GGCCGAGTGCAGTGA[C/T]TCACACCTGTAATCC	143279
rs191928365	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498716	CTTTTATGATCCCTC[A/G]TTCTTAATACAAATA	143279
rs191946004	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415272	GTATTTGGAACAATC[C/T]TGTATGAAAAATGTT	143279
rs192111524	snp	C/G	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440321	AAGGACTTTTCGGTA[C/G]TTATTGAGAAAATTG	143279
rs192134214	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91488977	TTTCTGTTAGTTGTA[C/T]TCGTACAATGTCATG	143279
rs192159135	snp	A/T	0.00438332	0.0466095	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91466804	TTCCATATCATGGAA[A/T]TTATTCAGTGATAAG	143279
rs192162763	snp	A/G	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491972	ACCTCAGCCTCCCAA[A/G]TAGTTGGGATTACCA	143279
rs192172685	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490694	CAGGAGATCGAGACC[A/G]TCCTGGCTAACACGG	143279
rs192211465	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437036	TTTCTTTAACAGATA[A/C]GGAGTATGAGATTCT	143279
rs192232306	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482100	GACACGAAGCTCAGA[A/T]TTTAGGTGAGTATAT	143279
rs192338818	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425027	CTCTGTTAAATCTTA[C/G]AGTAAATCTATAAGA	143279
rs192402326	snp	C/T	0.0271762	0.113356	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451000	ATTTAACCTAGCAAT[C/T]CCGTTACTGGGTTTT	143279
rs192402717	snp	A/G	0.0023933	0.0345097	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470633	ACACCTAGAAAATCT[A/G]CAGAAACAAGCACAA	143279
rs192406632	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470985	AGAGACACACACACA[C/T]ACACGCACACACACA	143279
rs192417548	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497766	ATTTTCATAGGAATA[G/T]AAATTGAAAGTGAGA	143279
rs192418556	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419408	GTTAATAGCAGAACA[C/G]GTACTCTAAGTGTTT	143279
rs192443393	snp	C/T	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426603	ACACACACACCCCTC[C/T]GTCACGCCAATATTG	143279
rs192465144	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91515126	ATTCATTTGGCCCTT[G/T]TCCCCTTGTCCACAT	143279
rs192504797	snp	A/G			intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462515	CTTAAACATTAGCCT[A/G]TATCAGAATCACAAG	143279
rs192543832	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91465009	CACTAAAAAATTTTC[A/G]TACATAGTAGTTTAA	143279
rs192646196	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420913	TCCACAGCCATTCCT[A/G]CACAAAGAATAACAG	143279
rs192653258	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91454816	TGAGTGAGAACATGC[A/G]GTGTTTGGTTTTTTG	143279
rs192665888	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91475911	AACCATCCCATGGTG[A/G]CCCTGGAGGTGGGGA	143279
rs192684729	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91408405	AAGTGGTTTCTCATC[C/T]AAACATTTTTATAGC	143279
rs192693245	snp	A/G	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503238	GCGGTCAGAATGGCT[A/G]TTGTTATATTAAAAA	143279
rs192700020	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432736	TCTGACATTTACCTT[A/G]AGAGCAAGCTCATAG	143279
rs192721509	snp	A/G	0.0271762	0.113356	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450707	CATCAAAAAGTGGGC[A/G]AAGGATATGAACAGA	143279
rs192758321	snp	A/G	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415914	CAAGAGACTTAATAC[A/G]TAAAAAGGGAGGGCT	143279
rs192759976	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497207	TCTCGAACTCATGGC[C/G]TCAAGTGATCCGCCT	143279
rs192817962	snp	A/T	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483374	TTACGTATCTCAAAG[A/T]TGGTGACTGGATTTG	143279
rs192821158	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451458	AAACCACCATGGCAT[A/G]TGTATACCTATGTAA	143279
rs192875315	snp	A/G	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476892	GATAAAAACCCCTGC[A/G]GGTCCGGGCCGGGCG	143279
rs192942905	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433337	TCTCTTTTCTGTTAT[C/T]TCTTGTATTCTTTCC	143279
rs192948280	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476381	TCCAGGATCACCACA[C/G]CTGCTCAATCACCCA	143279
rs192996723	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91428921	AACACTATGTTGAAT[A/C]GGAGTGGTGAGAGAG	143279
rs193028180	snp	A/C	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509302	ATTTAAAAAAAAAAT[A/C]AAAAAATAGCAGATG	143279
rs193032215	snp	C/T	0.00398564	0.0444627	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471711	CAATTCCACTCACAA[C/T]AGCCACAAAAAGAAT	143279
rs193144185	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445896	TACAACCTACAGACA[A/G]GGAGATTCTCTTGGG	143279
rs193160512	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409605	CCGTCCAATCCTATG[A/G]GGGAAGGGGAAAGGG	143279
rs193167861	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502763	ATTTCCAATTTTAAA[A/G]GAGTAATCTGAGCAA	143279
rs193175210	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91455225	TCTACATCCTCTCCA[G/T]CACCTGTTGTTCCCT	143279
rs193292313	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421785	AAGATGCCCTCTTCT[A/G]TACAGTGAGGTGTCA	143279
rs199567769	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91453001	GATGTGAGGAAAGGG[C/T]AAAGAAGGTGATAAA	143279
rs199629618	in-del	-/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439013	TGCAAACATTTTCTC[-/T]CATTCTGTAGGTTGC	143279
rs199653822	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438439	TGGCTGCATAGTATT[A/C]CATGGTGCATATGTG	143279
rs199682080	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437616	TTTGGTTGGATGGTT[G/T]TTCTTTTTTTTTTTT	143279
rs199691393	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449855	AAGGAGAACTACAAA[C/T]CACTCCTCAAGGAAA	143279
rs199718349	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91479175	AGCCAAGATCATGCC[A/G]CTGCACTCCAGCCTG	143279
rs199743994	snp	A/C	0.000186209	0.00964728	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500484	TAATTATTGTTTTTG[A/C]TAAATAATTATTGGC	143279
rs199795333	snp	A/G	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449158	ACCAAATGTAGCAGC[A/G]CATCAAAAAGCTCAT	143279
rs199800784	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437373	GCATCCTCACAGCAT[A/G]GTGACGGAATTCCAA	143279
rs199855841	snp	C/T	0.00199803	0.031544	synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484633	GTGGATTCCATCAGC[C/T]GCTAAAGTGTTGGCT	143279
rs199866659	in-del	-/AC/ACAC/ACAG	0.354644	0.233517	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497313	TTTTTTCTGCCCAAG[-/AC/ACAC/ACAG]ACAGTCTTGCTCTGT	143279
rs199997707	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439383	TCAAAGATCAGATTA[C/T]TGTAGATGTGTGGCA	143279
rs200036236	snp	A/G	0.00199798	0.0315436	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491242	AGACAGAGACCTGAT[A/G]TGAATATATTATTTC	143279
rs200042250	snp	A/C	6.80573e-05	0.00583301	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496383	TGCCTGTAAGTATAA[A/C]GTTATTAATATCTTG	143279
rs200052503	in-del	-/T	0.26078	0.249767	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496965	TTCTTTTTTTTTTTT[-/T]GAGACAGAATCTCAC	143279
rs200088865	in-del	-/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493789	CACTAATTTAAGGCA[-/T]TTTTTTAAAAAAAAT	143279
rs200095480	in-del	-/A	0.0103295	0.0711199	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91475534	GATAATTGATGACTT[-/A]TAATAAGAGTCTAGT	143279
rs200118662	in-del	-/CTTT	0.0232847	0.105357	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501132	GCTTCCTTTATATTA[-/CTTT]CTTTATTATAGGATT	143279
rs200120923	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91423092	TAAAAGTAGAGATTA[C/T]ATCAGCCACAAAGGG	143279
rs200125717	snp	A/G	0.00112622	0.0237032	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461230	TTTCTATATGTATAT[A/G]CGGTTAATGTGTTTT	143279
rs200174448	in-del	-/T	0.030278	0.119257	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91436038	TTTTTTATAGTACCC[-/T]TTTATTTCATGGTTA	143279
rs200185627	in-del	-/A			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91418186	CTAGATGTTTTTGTT[-/A]AAAAAAAAAGAACAA	143279
rs200205700	in-del	-/AC			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91416579	TAGATTTGTATAAGT[-/AC]ACTCTGTGATGTTTG	143279
rs200235313	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91441908	TTTTTTTTTTTTTTT[C/T]TTTTTTTTTTGCTTT	143279
rs200264319	snp	A/G	0.00199806	0.0315443	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512373	AATTCAGAAGGTTTT[A/G]GACTTGAGTAACCTA	143279
rs200272090	in-del	-/AAGA	0.0146672	0.084371	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91504609	ACGAGCAAAGCCTCC[-/AAGA]AATATGGGACTATGT	143279
rs200289813	snp	A/G	0.00367679	0.0427186	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500470	AAACCATCACTCTTT[A/G]ATTATTGTTTTTGAT	143279
rs200328171	snp	A/G	0.000502412	0.0158415	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496165	CATAATTCAGAACTC[A/G]TTTGTTGTCATGGAT	143279
rs200366539	in-del	-/AT	0.0158469	0.0875917	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91495773	CTCTGTTCTTCACAC[-/AT]AGTCTGTTTTTAATT	143279
rs200381333	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493774	ATATAATTGAAGTTA[G/T]CACTAATTTAAGGCA	143279
rs200394405	in-del	-/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91424457	AAGTGGATGTTAAAA[-/G]AAGTTAACTACTGTA	143279
rs200398909	in-del	-/CG			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471011	ACACACAGACACACA[-/CG]CACACACACAAAGAA	143279
rs200421586	snp	C/T	1.6525e-05	0.00287441	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478236	AGTATTAAAGGGAAT[C/T]ATTAACAGCCTGTTA	143279
rs200426220	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91436974	GAATTTCGGGAGGAA[A/T]TAAAATATGCTCAGT	143279
rs200442528	snp	A/G	0.000313374	0.0125135	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460528	GTCCTTCCAGAACCT[A/G]TTCTTCCTATCCAGC	143279
rs200459408	snp	C/T	0.00517822	0.0506191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439925	TGTGATTTTTGCACA[C/T]TGATTTTGTATCCTG	143279
rs200477012	in-del	-/TAT			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91417388	CTTTTTTTTTATTAC[-/TAT]ACTTTAAGTTTTAGG	143279
rs200477290	snp	A/T	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91504489	AAGAATGCAGAAGCC[A/T]CAGGAGCCAATGCGA	143279
rs200486088	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449860	GAACTACAAATCACT[C/G]CTCAAGGAAATAAGA	143279
rs200603397	in-del	-/AG			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91447723	AGAAAAAAAAAGAAA[-/AG]AAAAAAAGCAAGGGT	143279
rs200622964	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487053	TAGTTTGTGGCTTTT[A/C]TGCATAGCATAGAAT	143279
rs200648723	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419511	AGACCATTGAAGCCC[A/T]CATTAGGTACTTGTG	143279
rs200657287	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91429689	TTGTAGTATTCTCTG[A/G]TGGTAGTTTGTATTT	143279
rs200671325	in-del	-/AAGT	0.0652144	0.168387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449819	GCAATACAACTTACA[-/AAGT]ATGTGAAGGACCTCT	143279
rs200710574	snp	C/T	4.94629e-05	0.00497283	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460492	TCTATGGATGCATCA[C/T]CATCCGAAATGAAGG	143279
rs200780147	snp	A/G/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439626	CTGTGAAGAAAGTCA[A/G/T]TGGTAGCTTGATGGG	143279
rs200799289	in-del	-/GTCT	0.0154538	0.0865337	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460791	AAACACTAAGTAAGA[-/GTCT]GTGAGTCAAAACAGG	143279
rs200842761	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420711	AACAGAGACTGGCTG[G/T]TTTTTGTGCCTCTGC	143279
rs200846957	in-del	-/A	0.257732	0.24988	intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91463100	AACCCCCTATGCAGT[-/A]AAAAAAAAAATCTGT	143279
rs200849445	in-del	-/AG			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497315	TTCTGCCCAAGACAG[-/AG]TCTTGCTCTGTTGTC	143279
rs200899657	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91506373	AAAATTGATAGACCG[C/T]TAGCAAGACTAATAA	143279
rs201006647	in-del	-/A			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91418669	TAATAGGGAACTGTG[-/A]AAAAAAAACCATACA	143279
rs201023494	snp	G/T			intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91489191	AAGGAGAATGGCAGG[G/T]GTAGACTCTGTGACA	143279
rs201055708	snp	A/G	3.46069e-05	0.0041596	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498892	TCAAGAAGAATTTGG[A/G]ATAATCAAGTCCTAT	143279
rs201074905	in-del	-/G	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91494206	AAGTATAAAAGGGGT[-/G]GGGGGGGAATTCTTA	143279
rs201083243	snp	C/G	1.67225e-05	0.00289154	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512426	TATATGTAGCATTCA[C/G]TTCCCTCTTACTGTG	143279
rs201097146	in-del	-/A	0.0185938	0.0946107	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478828	GTATATTATTTAAAT[-/A]ATAACTTCCATTAAA	143279
rs201146161	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440261	TCCCATCAATACCTA[A/G]TTTATTGAGAGTTTT	143279
rs201263662	snp	A/G	0.00112126	0.0236511	intron-variant, missense	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462194	AATACTGTAAGTATT[A/G]TGACATGCAAGTAAT	143279
rs201273749	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451426	CTTAATGTAGATGAC[A/G]GGTTGATGGGTGCCG	143279
rs201292288	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91416038	AGTCTCTTTGTCAAC[C/T]TTTTTTTTTAAACCA	143279
rs201319230	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91447720	AAAAAGAAAAAAAAA[A/G]AAAAAAAAAAGCAAG	143279
rs201388345	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91413728	GACTTGTGACAGGTA[C/T]GGATGAAGTGAACAA	143279
rs201405332	snp	A/G	0.00209989	0.0323348	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425407	TTCCCTAACATCAAG[A/G]ATGGTAAATAATTTT	143279
rs201433936	snp	C/T	3.30934e-05	0.00406763	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484565	CAATTTATTTCTTTA[C/T]GCCTGTTTCCTGCAA	143279
rs201470639	snp	A/G	0.00016487	0.00907786	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460491	ATCTATGGATGCATC[A/G]TCATCCGAAATGAAG	143279
rs201489116	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91454955	GTGCCACATTTTCTT[A/T]ATCCAGTCTATCATT	143279
rs201491069	snp	C/T	0.000338106	0.0129976	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425268	ACTGCAATGTTAACT[C/T]TTCTGTTTTCAGGGT	143279
rs201560060	snp	A/C	0.00299544	0.0385843	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487654	AAATACACCATTTTG[A/C]TTTTTCTTTTTTTCA	143279
rs201567480	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439308	ATGGCTAGCCAGTTT[C/T]CCCAGCACCATTTAT	143279
rs201604816	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450034	AAAAAACTACTTTAC[A/G]TTTCATATAGAACCA	143279
rs201609007	in-del	-/A			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450601	GCAGCCTACAGAATG[-/A]GAGAAAATGTTTGCA	143279
rs201621439	in-del	-/A			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468767	TTACCCCATCTCTAC[-/A]AAAAAAAAATTTTTT	143279
rs201636255	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439025	TCTCCATTCTGTAGG[C/T]TGCCTCTTCACTCTG	143279
rs201647187	in-del	-/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450691	CAAGAAAAAAAAAAA[-/C]CATCAAAAAGTGGGC	143279
rs201693036	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91506151	AAATTTATAGCACTA[A/T]ATGCCCACAAGAGAA	143279
rs201738782	in-del	-/AGT			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91479923	TTGTTGCTATTTTTA[-/AGT]TTTATCCTTTTATAA	143279
rs201876142	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426948	CTGGTGTGCTGTACC[A/C]ATTAACTCGTCATTT	143279
rs201925604	in-del	-/GAGCA	0.0325976	0.123435	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467170	AGTTGAACAGGCAAG[-/GAGCA]GCCTGCTCTTGCCAC	143279
rs201937944	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91466977	GAGGAACATCTGCCA[C/T]GGAGAGACTGGACAT	143279
rs201941426	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421731	TTTAGTAGTTACTCA[C/T]AAATCATGTTGATAA	143279
rs201945945	snp	A/G	5.11261e-05	0.00505573	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478294	TTCAATATTTAGCTA[A/G]TCAGTATAGATGTCT	143279
rs201987796	in-del	-/GTATG			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462023	AATTATGAAGGAATA[-/GTATG]GTTCAAATTTTACTA	143279
rs201993815	snp	A/G	0.000720127	0.0189617	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425445	ATTTTGGCTAAAAGT[A/G]TATTTTTAAATTATT	143279
rs202002505	in-del	-/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91434147	TCCTGTGAGTCAGAC[-/T]TTTTTTTTTCCTGTC	143279
rs202059417	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438713	TGTAAAAGCGTTCCT[A/G]TTTCTCCACATCCTC	143279
rs202173922	in-del	-/T	0.00795532	0.062565	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91414884	GAAAAGCTTAGACAG[-/T]TTTTTTTTCCCCCTG	143279
rs202191521	in-del	-/AAA	0.0154538	0.0865337	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91469068	ACAAAAATAAAAAAT[-/AAA]GAAGAATGAACAAAG	143279
rs202233258	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439715	CTTCCTATCCATGAG[C/G]ATGGAATGTTTTTCC	143279
rs367546139	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503247	ATGGCTATTGTTATA[C/T]TAAAAAGTCAAAAAA	143279
rs367546472	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91505539	GAAGGCCATTACATA[A/G]TGGTAAAGGGATCAA	143279
rs367551097	snp	A/G	0.337614	0.234145	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91505981	ATCTCACTCAAAGCC[A/G]CTCAACTACATGGAA	143279
rs367554900	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91511936	GGGGATATTATGCAA[C/T]TCGAACAAGACCCCA	143279
rs367591168	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91465231	GGGAGATATAAATAT[A/G]GGATGAGGGAGGCTA	143279
rs367603140	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485339	GATTATCCACCTAAA[C/T]GAAATACTATTCAAA	143279
rs367676582	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483860	TTATCATTGAACTCA[A/C]GGCTAGCAGCACTGT	143279
rs367694159	snp	A/G	0.000124342	0.00788387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496410	CTTGTCCTTTAATGC[A/G]AAATCATCTTTTTTC	143279
rs367733481	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91459504	CAATAAAAATGAACT[A/G]TCTGTATATGCAACA	143279
rs367738903	snp	A/C	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500379	CGATTTTTCTTCAAC[A/C]AAAATGGTTTGATTT	143279
rs367790660	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477074	TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	143279
rs367915380	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487884	AGCATAATCAGGAAT[A/G]TTAAAAGCAAAATTC	143279
rs367920158	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461013	AGGGAAGGAAGGAGC[A/G]ATAATTGAGCGACAT	143279
rs367923681	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431741	TCCATCAGCTCCTTT[A/T]GGCACTTCTGTGTAT	143279
rs367960457	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91508933	TATACACCATGGAAT[A/G]CTATGCAGCCATAAA	143279
rs367983381	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437379	TCACAGCATGGTGAC[A/G]GAATTCCAAAGACAA	143279
rs368042968	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91456808	ACGGACGTAGGAAAA[A/G]AAGAGAAAATCAACC	143279
rs368051064	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91453775	CATGACCCAACTGTT[A/T]TCTATTTATAAGAAA	143279
rs368107150	snp	A/G	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485694	CAAAAGTAGCCTTAG[A/G]CAGGATGTAAATGAA	143279
rs368133711	in-del	-/TTAA	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91418207	AAAAGAACAAGACTC[-/TTAA]TTGATTGAGAATTTT	143279
rs368248100	snp	A/C	5.00321e-05	0.00500135	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500616	ACGGACTTAACTATA[A/C]AGTGAGCTCTTTATA	143279
rs368300708	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450461	ATTCAGGACATAGGC[A/G]TGGGCAAAGACTTCA	143279
rs368320743	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91465045	TAATCCTAACTAAAA[A/T]AACACATGCAAAGAC	143279
rs368348007	snp	C/T	1.65252e-05	0.00287443	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460439	CAGTGAGAGAACCAC[C/T]ACCAATTTGCCTTGA	143279
rs368401504	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91428534	TTCTTCCATTTGTTT[A/G]TATCCTCTTTTATTT	143279
rs368456855	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457477	ACACCATGACCAAAA[C/G]GTCACTCCAGGGATG	143279
rs368460589	in-del	-/A			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468404	AAAAGCCAAAAAAAA[-/A]TAAAATCCCATTCGA	143279
rs368524410	snp	C/T	8.32411e-05	0.00645086	intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462247	TATCAAAAGCAGCCA[C/T]ACAAATATTGTAAAA	143279
rs368607756	snp	C/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503718	GGCGCCCACCATTGC[C/G]CAGGCTTGCTTAGGT	143279
rs368619549	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440196	CTTTTGCCCATTCAG[C/T]ATGATATTAGCTGCG	143279
rs368633163	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457279	TACCAGAAAATAGAC[A/G]AAAAGGGAACACTTC	143279
rs368751833	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91443694	AACAGTCGCCCCTTC[A/C]CCCAGGAAGAATTTG	143279
rs368758745	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431136	TTTCTCCTTCACTTA[G/T]GAAGCTTAGTTTGGC	143279
rs368763364	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420778	CCTGTCTAAAATCTG[A/G]AAAGACTTCTGATTG	143279
rs368814529	in-del	-/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468110	CAAGCATGGATCCAA[-/C]CTGCCACTACCCCAG	143279
rs368829641	snp	C/T	0.000153719	0.0087656	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487805	ATAAAAACATATTTA[C/T]GCTGACTATAATCAG	143279
rs368862088	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449710	CAGGATACAAAATCA[A/G]TGTGCAAAAATCACA	143279
rs368901450	snp	A/C	1.6504e-05	0.00287258	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460541	CTATTCTTCCTATCC[A/C]GCCCAAAACTGTGAA	143279
rs368934451	snp	A/G	0.000153988	0.00877328	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460483	CAGCGTACATCTATG[A/G]ATGCATCATCATCCG	143279
rs368966238	snp	A/G	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438260	CTGACAGGTCCTGGT[A/G]TGTGATGTTCCCCTT	143279
rs368992277	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410649	CGGCCGGGCGAGGGC[C/T]GTCAGGAGGCCTGCG	143279
rs368996429	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503848	CAAACAAAAAGACAG[C/T]AGTAACCTCTGCAGA	143279
rs369025139	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431986	TAGACCTTTTAGCAG[A/T]CTTCCTTTATCTTAT	143279
rs369092207	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91466853	TCACAAAAAGACATG[A/G]AGAAACCTTAAATAC	143279
rs369118429	snp	C/T			intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482420	AAAAGTTGTCAGAAG[C/T]TGTATGTGTTTCTCC	143279
rs369176843	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449384	AAATTAGGTATTGAT[A/G]GAGTGTTTCTCAAAA	143279
rs369190810	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461769	GGCCAGGCTGGTCTC[A/G]AACTCCCGACCTCGG	143279
rs369190834	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490687	ACGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT	143279
rs369247176	snp	A/G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409092	ACTTAGGTACTCTTG[A/G/T]TCTAAAAATTCACTC	143279
rs369248260	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426587	ACACACACACACAAG[A/C]ACACACACACCCCTC	143279
rs369256492	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91472123	CAGACACATAGACCA[A/G]TGGAACAGAATAGAG	143279
rs369282749	in-del	-/A			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420281	AGCTTTTATGATTAC[-/A]AAAAAAAAAAAAAAG	143279
rs369284664	snp	A/G	0.000132183	0.0081286	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478210	CTACAGCCTCAAGAC[A/G]TTCAGAAGACAGTAT	143279
rs369339769	snp	C/T	2.04313e-05	0.00319613	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500451	ATAGTTCCAGTTTCA[C/T]TTAAAACCATCACTC	143279
rs369346204	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503212	AAACCACAATGAGAT[A/G]CCATCTCACAGCGGT	143279
rs369355342	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91423749	TCTCTTTGGGCTCTT[C/T]TATATTAATTTCTTT	143279
rs369356835	snp	A/C	1.65089e-05	0.00287301	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512338	AGGATCTGAAACAGA[A/C]ATTGATCATTGGAAT	143279
rs369398064	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91423483	CAAGCAAAAACAAAT[A/T]ACAATAAAATCTATG	143279
rs369464809	snp	A/G	0.000153988	0.00877327	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481184	TCTAAGTCAGATCTC[A/G]ATCCCTACATGTGTA	143279
rs369468108	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91448892	AGTAATTAATAGCCT[A/G]CCAACCAAAAAAAGC	143279
rs369497460	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483352	GCACATTCCTATTAT[G/T]GGTTTTTTACGTATC	143279
rs369583764	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91408782	CTTTTTGCTGACTAT[A/G]TGGCACTTATTCTAT	143279
rs369616973	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419792	GGTTGAGTATCCCAC[C/T]ACTATTCCTCAACAC	143279
rs369627968	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91475932	GAGGTGGGGACCTGA[A/G]GGAACAAATACCCCA	143279
rs369660237	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467231	GATTCCATGACCCCC[A/G]TGGACACTTGAGCTG	143279
rs369679114	snp	A/C	4.65214e-05	0.00482271	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425425	GGTAAATAATTTTTA[A/C]ATATATTTTGGCTAA	143279
rs369694891	snp	C/G	0.0174175	0.0916809	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409748	GGCTGCGCAAGCTCC[C/G]GGCCGCCTCTCCTGG	143279
rs369710190	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91473617	AGACAGGAAGACCAA[C/T]TCCTCCTCTTCAGCC	143279
rs369714296	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91510930	TTACTTGTATATTTA[C/T]ATGTCTATTTTTCCT	143279
rs369820677	snp	C/T	1.68185e-05	0.00289982	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484503	ATTTTGAAATCTTTA[C/T]CAGATTGTCCCAGAA	143279
rs369872084	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478350	ACATGTGTATGTATT[G/T]TACTCTCAGAAAAGA	143279
rs369887418	snp	A/T			upstream-variant-2KB, intron-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409393	CCTATTTGTAATGAT[A/T]TGATTGAGGACTGTG	143279
rs369899157	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444569	CCAAACTACAGGATG[C/T]GACATTCAGCTATTA	143279
rs369913271	snp	C/T	0.000153988	0.00877328	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501379	ATCTAAAGGTTACTG[C/T]TAATACTGCTAATGA	143279
rs369919924	snp	A/C	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452222	GGCTAAAAAAGTAAC[A/C]AAGTTATGACTGAAA	143279
rs369939363	snp	C/T	1.69789e-05	0.00291362	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485157	GTTGGAAAAAGTCTT[C/T]ATGTTAGAATTTATC	143279
rs369957761	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91479520	TAGTAATCTGTTTGC[A/C]TTTTCCTTCTTAAAC	143279
rs369977102	in-del	-/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91417339	GTGCCCTTTTTTTTT[-/T]GCTTTAGAGACTGCA	143279
rs369987034	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91506185	AGGAAAGATCCAAAA[C/T]TGACACCCTAACATC	143279
rs370145913	snp	A/G	3.32812e-05	0.00407915	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461220	CTGAATAATATTTCT[A/G]TATGTATATACGGTT	143279
rs370155595	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460887	ATTTATGATGTGACA[C/T]ATACTGTAAAAGTTA	143279
rs370285669	snp	G/T			intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464003	TTTAAGTCGTTTTTT[G/T]CAAACTAAGAAACAG	143279
rs370306196	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409505	GGGGAGAGAGCAAAA[C/T]GTAGGCGCGTGGGGA	143279
rs370353070	snp	A/G	0.00015133	0.00869726	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498996	TTAAAATGAATTAGT[A/G]TTTGCCATTTACTTT	143279
rs370382324	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91446343	CAACAAAAAGGATGT[C/T]CACACAAAAACCCCA	143279
rs370411502	snp	A/C/G	3.31928e-05	0.00407373	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462049	ATTTTACTAAGAATA[A/C/G]TCTTTAAAATGTTGA	143279
rs370438498	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421007	GTAATGTGCATAGTA[C/G]ATCTTCCCTCAAACC	143279
rs370457133	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492062	GAGTTTTTTTTAAAA[A/C]AAGAAATGAATTATA	143279
rs370459861	in-del	-/GGTTGTTTTG			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437639	TTTTTTTTTTTTTTT[-/GGTTGTTTTG]TTTTTTTTGTTGTTT	143279
rs370486053	snp	C/T	3.36338e-05	0.0041007	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425276	GTTAACTTTTCTGTT[C/T]TCAGGGTTTGGACAG	143279
rs370545106	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438350	TGGTTTTCTATTCCT[A/G]TGTTAGTTTGCTGAG	143279
rs370651945	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91510921	CTGAACAGGTTACTT[A/G]TATATTTACATGTCT	143279
rs370665862	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449807	ATAAAATACCTAGCA[A/G]TACAACTTACAAAGT	143279
rs370688946	snp	A/G	4.97368e-05	0.00498657	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492335	GTTCTCCTCTACTGT[A/G]TAATATCTTCAAATA	143279
rs370728381	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91504667	TGGTGTACCTGAAAG[C/T]GACGGGGAGAATGGA	143279
rs370775322	snp	C/T	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91494751	TCATTTGTTGAATGT[C/T]TCATCTTCATTGAAG	143279
rs370857441	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431115	GCTTGTCTGTAAAGT[A/G]TTTTATTTCTCCTTC	143279
rs370895708	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467777	TGCGTACCCCACCAG[G/T]CTACTGCTGCATGAG	143279
rs370900603	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91507040	ACATGATTATCTCAA[C/T]AGATGCAGAAAAGGC	143279
rs370953097	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471025	ACGCACACACACAAA[C/G]AAAACCTCAGGCCAA	143279
rs371038859	snp	C/T			intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482279	TTCAGGAGGTTTTTT[C/T]CAATAATATTTATTT	143279
rs371079776	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509893	ATGCAGTTTACCTTA[C/T]ATAACAAACCTGCAC	143279
rs371082635	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91424324	AATGCTTCTGCTATA[C/T]TATATGAGTGAATTC	143279
rs371162857	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91441919	TTTTCTTTTTTTTTT[G/T]CTTTCCATTTGTGTG	143279
rs371196542	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91428436	TTGGTAGCTTGATGG[G/T]GATGGCATTGAATCT	143279
rs371197008	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91454041	AACTGCAGGAGAAAA[A/G]CTGGTAGACCTGAAC	143279
rs371209430	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91428181	TGTCAAAGATCAGAT[A/G]GTTGTAGATATGTGG	143279
rs371228433	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91466316	CTTCCTTTTGTGATT[A/T]GTCTGGCTAGAGGCT	143279
rs371281896	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445569	GTTTAGACATTATAC[A/G]ATGAAAGAAGAGGGA	143279
rs371297506	snp	A/G	0.0193772	0.0965046	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91454914	TCATCCTTTTTTATG[A/G]CTGCATAGTATTCCA	143279
rs371300041	snp	A/G	3.33506e-05	0.0040834	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496222	TGCATAGCTTATGGG[A/G]CTAGCTGTTTATAAC	143279
rs371308612	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512751	CAGATTGTACACTGC[C/T]AGCACTGCTAGCACA	143279
rs371312306	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91508915	TTAAGAAAATGTGGC[A/G]CATATACACCATGGA	143279
rs371313445	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490666	GGAGGCCGAGGCGGG[C/T]GGATCACGAGGTCAG	143279
rs371385214	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500797	ATATGAAATCACTCC[C/T]TTTGGGAGAAAATTC	143279
rs371410759	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91434337	ACCAAAGTACTAAAC[A/T]GATACAGGGATCCTT	143279
rs371422869	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471161	TAGGATGCAAGGTTG[A/G]TTCATCCTACACATA	143279
rs371423104	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476431	AAACAATCATGACAC[A/G]GACCCCCACGAAGTT	143279
rs371549763	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467423	CAGACCTGGACAGAG[G/T]AGGGTGGTCTTGCCT	143279
rs371687878	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91494807	ATACTATGAGCTATT[C/T]ATATGTTCATACATA	143279
rs371704195	snp	A/G	0.0271762	0.113356	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476989	ATCGAGACCATCCTG[A/G]CTAACAAGGTGAAAC	143279
rs371714025	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476535	AAACAGGGCAGACAG[A/C]GCAAGAGGGAGGACA	143279
rs371770168	snp	A/T			intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481661	TTGATAGATACAGAT[A/T]AATAGATACAAAAAG	143279
rs371786899	snp	C/T			intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91407780	GCTCAGGTCTTCCAT[C/T]TGGACTTAGAAACAT	143279
rs371801389	snp	C/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440698	TTCACCTGTCAATCT[C/G]TCTGGTCCTGGGCTT	143279
rs371956804	in-del	-/CAG	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409221	TCTTTTCTCCTAGAT[-/CAG]CAGGTGTCCCCGCCG	143279
rs371997286	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91513096	CTAATTGGATTCAAG[A/G]TTATATTCTTTTAAG	143279
rs372002177	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91418594	AGTAGCTGACTTTTC[A/G]TATCTTAGTAGAAGG	143279
rs372018998	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477137	AGTGAGCCGAGATTG[C/T]GCCACTGCAGTACGC	143279
rs372063843	snp	C/G	8.25457e-05	0.00642386	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460544	TTCTTCCTATCCAGC[C/G]CAAAACTGTGAAAGA	143279
rs372075310	snp	C/T	4.95503e-05	0.00497722	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460442	TGAGAGAACCACCAC[C/T]AATTTGCCTTGATGT	143279
rs372103617	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91427911	CAATTTTGTCTTTTG[C/T]TGCCATTGCTTTTGG	143279
rs372117859	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433084	GTATTTTCAAGGCCC[A/G]AATAACTCCATCTAC	143279
rs372120035	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91465334	CATGTGTGTGCATGC[A/G]AGTGTGTATGTTCTA	143279
rs372185538	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440316	TATTGAAGGACTTTT[C/T]GGTAGTTATTGAGAA	143279
rs372193136	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91486098	ATTGTAGAGGAATCT[A/G]AGTAAAGAGATACAG	143279
rs372232483	snp	A/G	0.000144404	0.00849596	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425436	TTTAAATATATTTTG[A/G]CTAAAAGTATATTTT	143279
rs372257553	snp	C/T	4.95814e-05	0.00497878	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501302	GGCTGATTTGAACTT[C/T]AAAATCTCAAAGAAT	143279
rs372291905	snp	C/G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438239	CCTTCCCTAGTCCCC[C/G/T]ACTCACTGACAGGTC	143279
rs372302158	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444184	CTGGCTATAAACACC[C/T]ACAATTAAATACAAA	143279
rs372309196	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419064	GATACGGCTTTTAAA[A/G]CATTTCGTGATGGAA	143279
rs372324822	in-del	-/A	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481312	AGGATTAATAAGATT[-/A]AAAGATAAGTAAGAT	143279
rs372369805	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485913	ATGTTACAGAGAAAG[A/G]GCCTTACCACAGCTT	143279
rs372442098	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477560	TATTAAATATATATA[C/T]GTATATGTGTATATG	143279
rs372492518	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445644	TCCCAGTGAGATCAA[C/T]GCAGAAGGCAGGTGA	143279
rs372505235	snp	C/T	0.00755907	0.0610114	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91427536	TGACTTTTTAATGAT[C/T]GCCATTCTAACTGGT	143279
rs372548211	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412787	TTGGTCCTTAGTCCA[C/T]CCAAAGGATAAGAAA	143279
rs372553714	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487439	GTAAGTGGTTAGCAC[A/C]CATTCAGAACCTTTG	143279
rs372555483	snp	A/C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445589	AAGAAGAGGGAGTGG[A/C/T]TGGCAAGTCAGCCGA	143279
rs372556026	in-del	-/AA			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91473132	TAACAGGGGAAACAA[-/AA]TATATACTAAGCAAG	143279
rs372556308	in-del	-/AGCAG			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467171	GTTGAACAGGCAAGG[-/AGCAG]CCTGCTCTTGCCACG	143279
rs372558629	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410670	GAGGCCTGCGTTTAC[C/T]CTGGGCACGCCCTGG	143279
rs372562565	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91513302	TCTTTTGAATCATGT[A/G]CAAGACTTATATCTA	143279
rs372573956	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437648	TTTTTTGGTTGTTTT[G/T]TTTTTTTTGTTGTTT	143279
rs372599601	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449304	AAAAAACACTTAATT[A/G]CCTCAATAGATGTAT	143279
rs372658247	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91473188	TGAAATTGGAACATC[A/G]TAATAAAGATACCTT	143279
rs372679271	in-del	-/GC			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91441919	TTTTCTTTTTTTTTT[-/GC]TTTCCATTTGTGTGG	143279
rs372774990	snp	A/G			intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482216	TTGAGTTGTTCTGTC[A/G]ATAAGTCAGTTTTGA	143279
rs372846496	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91434761	ACATGAGTTTTGTAG[A/C]TTCTCAGGCTGGGTT	143279
rs372857702	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451956	TAAGATATTAATCAT[G/T]CTGTTGTTTTAGAAG	143279
rs372871562	snp	C/G	0.00318978	0.0398085	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91473262	TTATTTGGCTGTCAG[C/G]AGACTGCTCCACAGC	143279
rs372881382	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431089	GGTGGTGACAAAATC[C/T]CTCAGCATTTGCTTG	143279
rs372951895	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426585	ACACACACACACACA[A/C]GCACACACACACCCC	143279
rs372988036	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91507009	CAGCATATAAACAGA[A/G]CCAAAGACAAAAACC	143279
rs373060101	snp	C/T	1.6617e-05	0.00288239	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491281	AAAGTAAGACGGACA[C/T]ATCTGGTTAGCGATT	143279
rs373079219	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91474726	TTCTATTGGGGGCAG[A/G]TTACAGATAGAAAAT	143279
rs373134313	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91455413	CACCCACTTGTTGAT[A/G]GGGTTGTTTGTTTTT	143279
rs373145655	snp	G/T			upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409469	CAAGGAAGGGACGGA[G/T]AGGAGACAGCAAAGG	143279
rs373149300	in-del	-/AAAATAAT			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91423479	GACCAAGCAAAAACA[-/AAAATAAT]AATTACAATAAAATC	143279
rs373158654	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492699	AATCCTACACAAAAT[A/G]TATCAAGATTAAAAG	143279
rs373173631	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91504335	AATTACTCTGAGCTA[C/T]GGGAGGACATTCAAA	143279
rs373175410	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91430895	TTTAAAGTTAATATC[A/G]TTATGTGTGAATTTG	143279
rs373221732	snp	C/T	0.000214397	0.0103514	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493521	ATTGTATCCTTTAAA[C/T]TTTCCACTAGGAGGT	143279
rs373225909	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91513892	CTTTGAGGAAAAGGG[A/G]TCACTTTGTTTACTA	143279
rs373234657	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438464	TATGTGCCATATTTT[C/T]TTTATCCAGTCCATC	143279
rs373237698	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91427744	TTGTAGATTCTGGAT[A/G]TTAGCCCTTTGTCAG	143279
rs373251356	snp	C/G	1.6569e-05	0.00287824	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512386	TTGGACTTGAGTAAC[C/G]TAGAAGACTTGAAAT	143279
rs373263073	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91475277	CAATGAAAATAGAAA[C/T]GTTCAGACTCATATA	143279
rs373290833	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91505994	CCACTCAACTACATG[A/G]AAACTGAACAACCTG	143279
rs373323152	snp	A/G	1.65932e-05	0.00288034	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461226	AATATTTCTATATGT[A/G]TATACGGTTAATGTG	143279
rs373344630	snp	C/T	3.30825e-05	0.00406696	synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485223	CCTTATTCCTTATAC[C/T]GATTTCTATAATTCT	143279
rs373352820	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487454	ACATTCAGAACCTTT[A/G]ATGTAGCTTCTGCAG	143279
rs373374347	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91442236	AGTTTTCCTTTCCAT[A/G]TTTAGTGCTTCCTTC	143279
rs373427505	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91423750	CTCTTTGGGCTCTTT[C/T]ATATTAATTTCTTTA	143279
rs373466176	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499265	AGAAAATATTTTCTA[C/T]TTTTTAAAAGTAGAA	143279
rs373515674	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91469133	CAAATCTACAACTCA[C/T]TGACATCTCAGAAAG	143279
rs373521043	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450756	ATTTATGCAGCCAAC[A/G]AACATGAAAAAAGGC	143279
rs373580957	snp	G/T	1.69324e-05	0.00290962	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492532	TTTCTTCATAATTGT[G/T]AGAGTGAAGTAGTCA	143279
rs373726577	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91428452	GATGGCATTGAATCT[A/G]TAAATTACCTTGGGC	143279
rs373728412	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91454991	ACATTTGGGTTAGTT[C/G]CAAGTCTTAGCTATT	143279
rs373741183	snp	C/G	0.242775	0.249896	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91504839	GTCAGATTCACCAAA[C/G]TTGAAATGAAGGAAA	143279
rs373784503	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91494846	TCATGCTTTATATTC[A/G]TATATCACAATTTAG	143279
rs373843651	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499550	CCTGCTACCTCAGGG[C/T]TCCCTCAGCAACTCT	143279
rs373894169	snp	A/G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91474200	TCTTAACTGGAGAGT[A/G/T]GGGGAATGGGAAAAA	143279
rs373907920	snp	A/G	3.40315e-05	0.00412488	synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425346	TTCAGCTGTTAGCCC[A/G]AAGAAAGAAGCTGCT	143279
rs373926563	snp	A/G	0.000137219	0.00828194	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482922	TGTCTTTCCTTTTAC[A/G]TGTTAACAGAATTTT	143279
rs374013468	snp	A/C/G	0.00716266	0.059414	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438303	TGTTCTCATTGTTCA[A/C/G]CTGCCACTTACGAGT	143279
rs374023316	in-del	-/C	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91459783	TATATTTTTACTATA[-/C]CTTTTCTGTATTTAC	143279
rs374106635	in-del	-/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91417706	GAACTCATCATTTTT[-/T]ATGGCTGCATAGTAT	143279
rs374128613	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440448	GATTGTGGTGGATAA[A/G]CTTTTTGATGTGCTG	143279
rs374135734	snp	A/G/T	8.32891e-05	0.00645282	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512412	GAAATATAATCTTTT[A/G/T]TATGTAGCATTCACT	143279
rs374155110	in-del	-/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439014	GCAAACATTTTCTCC[-/C]ATTCTGTAGGTTGCC	143279
rs374164884	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499647	TTGTCTTAGCCATGT[A/G]AATATGGATCAGCTA	143279
rs374216853	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91443602	CCCTTAGCAGAGCTT[A/G]AGCGCTGTGCTGGGA	143279
rs374232314	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91459095	TCACTGAAGAAGATA[C/T]ATGGATGGAAAATAA	143279
rs374234589	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499534	ATATGTATAGCTGCT[G/T]CCTGCTACCTCAGGG	143279
rs374268371	in-del	-/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440557	TTTTGTTGTGTCTCC[-/G]CCAGGTTTTGGTATC	143279
rs374274723	snp	A/G	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464743	CCATGCTACCTGTGC[A/G]CCAAGGGCTTGGCCA	143279
rs374287983	snp	A/G			intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91489339	TCACTTGGAATTAAT[A/G]ACTGATGACTATTTT	143279
rs374291263	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484957	CATATTCCCTTTAAT[A/G]CTATTATAATCCTCA	143279
rs374296690	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458022	GCATAATTGTCTATG[A/C]AAAAAAAAAAAAAAA	143279
rs374313125	snp	A/G	1.66815e-05	0.00288799	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499191	TTTCGGTTAGCTTTT[A/G]TAGTACTATCATGTT	143279
rs374321702	in-del	-/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91414892	AGACAGTTTTTTTTT[-/T]CCCCCTGCGGTTAGT	143279
rs374342601	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439820	GTAAGTTGTATTGCT[A/G]GGTATTTTATTCTCT	143279
rs374348428	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478352	ATGTGTATGTATTTT[A/G]CTCTCAGAAAAGATT	143279
rs374454696	snp	G/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512929	AGTTGCTGAAAAGCA[G/T]GTAAATAACTACATA	143279
rs374501352	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444690	GATGATTCTTAAAAT[A/G]TAATTCAAAAAGAGA	143279
rs374546867	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91469635	GGAAAGACTGTTACC[A/G]GCTGCCACAAAAACA	143279
rs374554567	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420724	TGTTTTTTGTGCCTC[C/T]GCTATTCTCTTTTAG	143279
rs374557574	snp	G/T			intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91407844	CAAAGCGAATGAGTT[G/T]ATACTTGGATACCCT	143279
rs374587906	in-del	-/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421257	TTAACATTATTGACC[-/T]TTTTTTTTTTCTTGA	143279
rs374715314	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91427973	ATGTCCTGAATGGTA[A/T]TGCCTAGGTTTTCTT	143279
rs374771231	snp	C/T	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451231	TTGCAGGGACATGGA[C/T]GAAGCTGGAAAGCAT	143279
rs374773119	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91434484	AGCCCTCTTGTTTTT[C/T]ATTTTGTCAAAACAT	143279
rs374775084	snp	C/T	1.66671e-05	0.00288674	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485346	CACCTAAATGAAATA[C/T]TATTCAAAAGAATGA	143279
rs374838690	snp	G/T	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91418356	CCTTGCCTTCCTAGT[G/T]ATAAATGAACTGAAA	143279
rs374871869	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91494689	CACAAAATGAATAAC[A/G]CTTAACAATTCTGAG	143279
rs374874572	in-del	-/A			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500145	TCTACAGTGCACACA[-/A]GGAGGTGTTATGGGA	143279
rs374930274	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491729	TATATTGGGTCTATA[C/T]AGGTTCTAACATACT	143279
rs374939323	snp	A/G	0.00636936	0.0560724	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477050	GCCGGGCGCGGTGGC[A/G]GGCGCCTGTAGTCCC	143279
rs374944381	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426586	CACACACACACACAA[A/G]CACACACACACCCCT	143279
rs374955379	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492507	TGTAATCTAATTTTT[A/G]TAAACTGTGTTTCTT	143279
rs375007221	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91469068	ACAAAAATAAAAAAT[A/G]AAGAAGAATGAACAA	143279
rs375011462	in-del	-/GAAA			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471025	ACGCACACACACAAA[-/GAAA]ACCTCAGGCCAATAT	143279
rs375041509	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91465645	TTTTATCATGAATGG[A/G]TATTGGATTTCATCA	143279
rs375070922	snp	C/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91456661	TCTTGTGCCAGTTTT[C/G]AAAGGGAATGCTTCC	143279
rs375133745	snp	A/G	0.000154799	0.00879633	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498828	TCACCAAAGTATGTT[A/G]TTATATCAACCATAT	143279
rs375168282	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91416023	ACCACAAAGCCGTAA[A/T]GTCTCTTTGTCAACT	143279
rs375175715	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91510145	GCCTCTTAGAATAAA[A/G]TCCATGGAGAAAATA	143279
rs375212434	snp	C/T	8.29896e-05	0.00644111	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500607	TATGCAAAAACGGAC[C/T]TAACTATAAAGTGAG	143279
rs375224289	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91495651	GCTTTTTAACTTTGA[C/T]ACTGAAACTCCAAGT	143279
rs375236737	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91488020	GAAGAGTAAATGCTT[C/T]TCACAGATTCAAATT	143279
rs375285120	snp	A/G	3.35182e-05	0.00409365	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512220	TAGCAGTCATTTTGT[A/G]TGTGTTTCAAGACTT	143279
rs375287809	snp	A/C/T	1.65296e-05	0.00287481	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462077	TGAATATACTTAATT[A/C/T]TTAAATTGAATTTGC	143279
rs375342246	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91428418	GTTCTGTGAAGAAAG[G/T]CATTGGTAGCTTGAT	143279
rs375343857	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490920	AAAAAAAAAAAAAAA[A/G]AGATGAGACATACGG	143279
rs375388660	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476290	AGAATTTACATAGGG[A/G]CAGTGAATCTGTTAT	143279
rs375400075	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467434	AGAGTAGGGTGGTCT[C/T]GCCTGTGAGATGGTG	143279
rs375432316	snp	A/G			synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410459	TGAGGCGGTTCGGGT[A/G]CCCTCGCCCGCCACT	143279
rs375546547	snp	G/T	0.00557542	0.0525036	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91513185	TTGTATAATGATCAT[G/T]TCTTCTTAAGGCTCA	143279
rs375581082	in-del	-/AAG			upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91408652	ATTTCAGTAGTTTTA[-/AAG]AGGAAAGAAAATCCT	143279
rs375605955	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91511812	CAACAACCATACCCA[A/T]CTCTGGCCCTGGGGT	143279
rs375613282	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91475924	TGACCCTGGAGGTGG[G/T]GACCTGAGGGAACAA	143279
rs375717204	in-del	-/TTG			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491113	TGGCATAGATAATAA[-/TTG]TTATTTTTACTAAAG	143279
rs375785547	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421806	TGAGGTGTCAAAATA[C/T]GCCTATTCTTCTGAA	143279
rs375789737	snp	A/T	0.000500333	0.0158087	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512249	TTAGTATTTTTTTTT[A/T]ATTTTTTTCCCTAGC	143279
rs375802162	snp	C/T	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440210	GTATGATATTAGCTG[C/T]GGCTTTGTCATAAAT	143279
rs375823565	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509914	AAACCTGCACATGTA[C/T]CCCTGAACCTAAAAT	143279
rs375841690	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426209	TAGAATTGTGTATAT[A/G]TTATTAATGTTTCTT	143279
rs375885053	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91446121	AACACCACATACAGG[A/G]GAGCTCCAGCTGGCA	143279
rs375885267	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91475154	ATAGTTAAGAAAGAT[C/G]TCTCTAGATGCTTAG	143279
rs375907537	in-del	-/TTTTTTTTTTTTT			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497457	CACCACACCTGGCTA[-/TTTTTTTTTTTTT]TTTTTTTTTTTTTGG	143279
rs375926476	snp	A/C/G/T	0.000212591	0.0103082	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496409	TCTTGTCCTTTAATG[A/C/G/T]GAAATCATCTTTTTT	143279
rs375929643	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485915	GTTACAGAGAAAGGG[C/T]CTTACCACAGCTTAT	143279
rs375935105	in-del	-/A/AA			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468939	GACACTGTCTCACTC[-/A/AA]AAAAAAAAAAAAAAA	143279
rs375978453	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91480719	ATGAACCTAGAAACA[A/C]AAGCATATTTTCTTT	143279
rs375981412	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439292	TTTCAGTTTTCTGCA[G/T]ATGGCTAGCCAGTTT	143279
rs375984616	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457435	AATATTAGCAAATAA[A/C]ATTCAGCAATATGTA	143279
rs376086817	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91505954	CAATCAAACTAGAAC[A/T]CAGGATTAAGAATCT	143279
rs376090534	snp	A/C	3.30196e-05	0.00406309	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461300	GATTGGAAAGCAGTA[A/C]ATGATTTTTATCTAA	143279
rs376120367	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438344	AGTGTTTGGTTTTCT[A/G]TTCCTATGTTAGTTT	143279
rs376154221	in-del	-/CCCCCCCCCC			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464794	ACACAGCCCACCTCA[-/CCCCCCCCCC]CAGCCACTCAGCCTA	143279
rs376155205	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91508818	TGCTATAAAGACACA[G/T]GCACACATATGTTTA	143279
rs376230143	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91430947	CTGGTTATTTTGCTC[A/G]TTAGTTGATGCAGTT	143279
rs376231255	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483782	CAGCCAATCAGTATA[C/T]AACTTTGCTTTATGA	143279
rs376236561	in-del	-/GGA			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497483	TTTTTTTTTTTTTTT[-/GGA]TTTTTAGTAGAGACA	143279
rs376302309	snp	A/T	6.67189e-05	0.00577538	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512248	CTTAGTATTTTTTTT[A/T]AATTTTTTTCCCTAG	143279
rs376350745	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91428158	CCATTGCTTGTTTTT[C/G]TCAGGTTTGTCAAAG	143279
rs376510687	snp	C/G	1.65348e-05	0.00287526	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478204	TTTTGCCTACAGCCT[C/G]AAGACGTTCAGAAGA	143279
rs376513254	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91418946	GAAAAAGTAGTTTTT[A/G]TATGCATCACAGATT	143279
rs376526901	snp	A/G	3.44453e-05	0.00414988	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481045	TTTTCGTTAGATGCT[A/G]TGAGATTAAACATTC	143279
rs376552931	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91508978	TGTCCTTTGTAGGGA[C/T]ATGGATGAAATTGGA	143279
rs376557393	snp	A/G	0.000275962	0.0117433	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481191	CAGATCTCAATCCCT[A/G]CATGTGTATGTGAAA	143279
rs376610422	snp	C/G	0.000149364	0.00864058	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492320	TTTTCACTGCTCTTT[C/G]TTCTCCTCTACTGTA	143279
rs376618177	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91414847	AAAGATTGCATGGGG[A/G]CTGGAGCCAGATCAC	143279
rs376759893	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91408779	ATACTTTTTGCTGAC[C/T]ATATGGCACTTATTC	143279
rs376765068	snp	A/G	0.000121428	0.00779096	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491327	AATTTATTCCAAAAT[A/G]ATATTAATTAAAGCT	143279
rs376782401	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91416313	AAACATTTAGAAAAA[A/G]ACCTTGTACAAAGCA	143279
rs376821335	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91427914	TTTTGTCTTTTGTTG[C/T]CATTGCTTTTGGTGT	143279
rs376869282	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91427904	CATTTGTCAATTTTG[G/T]CTTTTGTTGCCATTG	143279
rs376877957	in-del	-/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421267	TTGACCTTTTTTTTT[-/T]CTTGAAACTTTATCC	143279
rs376950821	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477151	GCGCCACTGCAGTAC[A/G]CAGTCTGGCCTGGAT	143279
rs376954622	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91469256	TTCAGGAAATTCAGA[G/T]AACCCCTGCAATATG	143279
rs377033564	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440586	TCAGGATGATGCTGA[C/T]CTCATAAAGTGAGTT	143279
rs377042111	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91510498	TCTTCTGGTAGAATA[C/T]TGATATTGTTTTCTT	143279
rs377076615	snp	C/T	5.70847e-05	0.0053422	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482940	TTAACAGAATTTTAA[C/T]ACAATTATCTTTAAT	143279
rs377164506	snp	A/C	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458311	AGGCATACTGTGTTC[A/C]TGGATTAGAACACTT	143279
rs377166472	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91479815	CTTCATTGGTATCTT[C/T]TTTTAACAAAACTTG	143279
rs377226501	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91428504	TTGATTCTTCCTACC[A/C]ATGAGCATGGAATGT	143279
rs377228146	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91455914	TTCTGAGGGCTCTGT[G/T]CTGTTCCATTGGTCT	143279
rs377313181	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460099	CATTGAAATACCCCC[A/G]GAAAGATGACTTTTG	143279
rs377314758	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91424068	TAACATTGGTCAGGA[C/T]TGGCTCTGTTTCACA	143279
rs377342538	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493001	TTCAGTGTTTTCCTT[A/G]TTCTTTAGTTTTCTT	143279
rs377453121	snp	C/T	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420274	TTGTTTAAGCTTTTA[C/T]GATTACAAAAAAAAA	143279
rs377492263	snp	A/G			intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91463309	TAAAATATATTTACT[A/G]TATATTAAGTGGAAG	143279
rs377506261	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91511534	GGTTTTGTGGAAGAC[A/G]GTTTTTCCACAGAAC	143279
rs377527773	snp	C/T	0.221737	0.248397	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91504670	TGTACCTGAAAGTGA[C/T]GGGGAGAATGGAACC	143279
rs377574287	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444920	TGATAAGCAGTAATC[A/G]TTTTCCCTTTCTTTT	143279
rs377596458	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476131	GATAGGAATGTTTTA[A/G]TAGAGAGGGAGAAAC	143279
rs377622400	snp	G/T	1.67158e-05	0.00289096	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496219	GTATGCATAGCTTAT[G/T]GGACTAGCTGTTTAT	143279
rs377652955	snp	A/C	4.99073e-05	0.00499511	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512407	GACTTGAAATATAAT[A/C]TTTTATATGTAGCAT	143279
rs377655673	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464739	CACACCATGCTACCT[C/G]TGCACCAAGGGCTTG	143279
rs377693022	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91428485	TATGGCCATTTTCAC[A/G]ATATTGATTCTTCCT	143279
rs377718017	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91469984	AGACAAGAGCATTAC[A/G]TAATGGTATAGAGTT	143279
rs377718796	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91455019	ATTGTGAATAGTGCC[A/G]CAATAAACATACGTG	143279
rs377728320	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426249	TATATTGTTTTATCA[C/T]GGGAAATGTACATTA	143279
rs386746515	multinucleotide-polymorphism	ACG/CCA			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91418678	AACTGTGAAAAAAAA[ACG/CCA]TACAAAAAGAGAAAC	143279
rs386746516	multinucleotide-polymorphism	CG/TC			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450076	ATATAGTCAAGACAA[CG/TC]CTAAGCAAAAAGAAC	143279
rs386746517	multinucleotide-polymorphism	CA/TG			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450155	GTAACCAGAATAGCA[CA/TG]GTACTGGTACCAAAA	143279
rs386746518	in-del	ACA/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470984	CAGAGACACACACAC[ACA/G]CACGCACACACACAC	143279
rs386746519	in-del	CA/CACA/GACACACACG			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471003	ACGCACACACACACA[CA/CACA/GACACACACG]CACACACACAAAGAA	143279
rs386746520	in-del	AAG/CACACAC			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471023	ACACGCACACACACA[AAG/CACACAC]AAAACCTCAGGCCAA	143279
rs397705759	in-del	-/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91434635	TGTTCTTCTTTTTTT[-/T]GGGACATCTTATAGT	143279
rs397705760	in-del	-/AAG			upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91408654	TTCAGTAGTTTTAAG[-/AAG]GAAAGAAAATCCTGA	143279
rs397846279	in-del	-/GT			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415230	TGTGTGTGTGTGTGT[-/GT]ACTTAACAACAATAT	143279
rs397847297	in-del	-/A			utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91513345	CCAGTTGTACCAAAA[-/A]CACTAATTTTTGAAA	143279
rs397965322	in-del	-/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490233	TCCTACTTTCTTCAG[-/G]TGTACCTTCCTTGTA	143279
rs397970630	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426504	TTATAGGTTAGTATT[A/T]TATTGCCTCATTTTT	143279
rs398014422	in-del	-/A	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91416047	ATGGCTTTGTGGTTT[-/A]AAAAAAAAAGTTGAC	143279
rs398097139	in-del	-/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410610	CCGTCTGGCGCCCCG[-/G]ACGGCGGGAGTTGGG	143279
rs527262442	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477406	TGTGGTCATAAACTT[A/C]AAGTATGTCCAGTCA	143279
rs527273778	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91414741	AAAGTAATCCAGTGA[C/T]GAAAACAGCATGAGC	143279
rs527286052	snp	G/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422928	GAAGAGGTGAAGGAA[G/T]GGGGAAGAAAAGAAA	143279
rs527295367	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91413768	GAAATCAGGCGTGGT[A/G]GGGAATTGAAAGAAA	143279
rs527320791	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91465050	CTAACTAAAAAAACA[C/T]ATGCAAAGACTATAA	143279
rs527378866	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482608	TTATGAAGGTGCTTT[A/G]TATACATTTTCTTTT	143279
rs527450062	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91514659	TCAGTCATATTTTTG[C/T]CTGTATGATTAGAAG	143279
rs527468342	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509628	CATGTCCTTTGCAGC[A/T]ACATGGATGAAGCTA	143279
rs527498142	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91513236	GACCTAAATAATCAT[G/T]GATGAAGTATGTCAG	143279
rs527504619	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91407399	TTAAAAATCCACAAC[C/T]ATTATACCTAAGAAA	143279
rs527512888	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425971	ATATTAGTTAACTAA[A/G]TTATGTTAATCTATA	143279
rs527553779	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457615	TAATGAAAAAAATTA[A/G]AACTCCCAGAAAAAT	143279
rs527586082	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421842	AAGAAAGCATTTTAC[A/G]TTGTTTATTTCACTT	143279
rs527588606	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457547	CACCATACTAACATG[C/T]TAAGAATGATTCCAT	143279
rs527646435	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91511243	AGGAAAGAGTCTTAA[C/G]ATAGCTGTAAGAATC	143279
rs527745821	snp	A/G	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91455193	TCCCACAAACAGGGT[A/G]AAAGTGTTCCTATTT	143279
rs527801822	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462500	TGTAGATCAGTGGTT[A/C]TTAAACATTAGCCTG	143279
rs527821461	snp	A/C	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412839	ATTGACTTTTACAGC[A/C]GCTAGGAAGGCCTTG	143279
rs527834860	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492588	TTTTACAGACTTTTT[C/G]TCCATCGTAAATGTT	143279
rs527867743	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431179	TCTGGGTTGAAAATT[A/C]TTTTCTTTAAGAATG	143279
rs527895959	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91430651	GCCTTCTTTGTCTCT[C/T]TTGATCTTTTTTGGT	143279
rs527930838	snp	A/G	0.00279162	0.0372561	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451258	GCATTATTCTCAGCA[A/G]ACTATCACAGGAACA	143279
rs527960861	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437955	ACAAAACACTTTTTT[A/T]AAAAAAACAATTTAT	143279
rs527968626	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502239	TTTTCATTTCTTTCT[A/G]TGCTTTAGTCAACAG	143279
rs527972488	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501959	CATTTTTGTCTCCTG[C/T]CCCATACATTGAACA	143279
rs527978254	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491761	TGATTGCATTTTCAT[A/G]TATTATCATAAAAAA	143279
rs527993800	snp	A/G	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91473090	CTGGGAGTTTCCCAT[A/G]ACTGATGTAAGACGT	143279
rs528008055	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501416	ATTTGGAATCAGGAT[A/G]TGTACTCCGTTTGAA	143279
rs528011429	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470396	AATCCATACTGAGAA[A/G]ACCACTCAAAAGCAT	143279
rs528061311	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91453219	GGAGGATGGCCTGAG[A/G]CCAAGAGTTTGAGAC	143279
rs528133804	in-del	-/CAGT	0.0023933	0.0345097	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91514753	AATATTAAAATTATA[-/CAGT]CAGTCAGGCTTCAGT	143279
rs528136766	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91459722	TCATGACATTTCAGT[C/T]AAGAATAGACCACAT	143279
rs528161022	snp	A/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91513601	TACAGCAAATGAAGC[A/T]GTTTTATTAGCATGT	143279
rs528206462	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409194	AACAGGCGATACAGC[A/G]CATTCTTACTCTCTT	143279
rs528234329	in-del	-/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91510469	TTTCTTCAATAAACA[-/T]TTTCATAAGATATTC	143279
rs528292460	snp	A/T	0.0023933	0.0345097	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91427186	GACATGAACTCATCA[A/T]TTTTTATGGCTGCAT	143279
rs528344452	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444324	ATTAGTAAAAGAACT[C/G]GATTTTGGCAGAGCC	143279
rs528363198	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498497	ACATTAGAAGCTAGG[A/G]GTAGAAACTAATGAG	143279
rs528404367	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91505719	GACAGATCAACGAGA[A/C]AGAAAGTCAACAAGG	143279
rs528425861	in-del	-/A			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450690	ACAAGAAAAAAAAAA[-/A]CCATCAAAAAGTGGG	143279
rs528447416	snp	G/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484362	TAAGATTTTGTATCT[G/T]TTCAAATGTTTGGCA	143279
rs528461995	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432978	CTCTAAGAGCAACTT[C/G]AGGGGCAGGTGTTAG	143279
rs528471568	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91424120	TAACAGATGCTCTAA[C/T]ATGTCAACTCAGCCT	143279
rs528490546	in-del	-/AA	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91456809	CGGACGTAGGAAAAG[-/AA]GAGAAAATCAACCGA	143279
rs528557405	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440000	GAGATGATGGGGTTT[C/T]CCAAATATATAATCA	143279
rs528625819	snp	A/G	0.00358779	0.0422022	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503559	CCACCCGAATACTGC[A/G]CTTTTCCGACGGGCT	143279
rs528672016	snp	C/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91417526	TCCCTCCCCGCCCCC[C/G]CACAACAGGCCCGGG	143279
rs528694740	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409666	TCCAGGCTTTTCCTG[A/T]GTAGGCTGAAGCCAT	143279
rs528703361	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91416784	TATATCAAGCCTCAG[A/G]CCCTGTATGTATTGC	143279
rs528754162	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91443780	GAAACACTCTTCCAT[A/G]GTTTTAAATGAGAGA	143279
rs528768282	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439613	GTTTTTTCTAATTCT[G/T]TGAAGAAAGTCAATG	143279
rs528791063	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91424798	ACATAAACTCTAAAG[C/G]GTTATCTTTTTACCT	143279
rs528812985	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415853	TTATGGTATGAATAG[A/G]TCATTAAATTATATG	143279
rs528848881	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91479386	CAAAAAAAAGAAGAA[A/G]GTAAAAAATGTTTAC	143279
rs528851036	snp	A/C	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491498	CAGATCTGTATTCAT[A/C]ATTGTCTTATATTCA	143279
rs528854158	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91430432	CAATTCCTGGGTATC[C/T]TTGTTAACTTTCTGT	143279
rs528854450	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420471	GCATGTGCCTATAAT[C/T]CCAGCTACTCAGGAG	143279
rs528868607	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91429381	TTGGTATCAGGATGA[A/T]GCTGGCCTCATAAAA	143279
rs528933837	snp	A/G	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503936	TGGAGATCTGAGAAC[A/G]GGCAGACTGCCGCCT	143279
rs528955948	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437082	TTCTGTTTATACATG[G/T]TCCAGTATCTATTGA	143279
rs528991543	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501042	AAAGTCTAATACGTA[C/T]ATAGAAGCTCACCAT	143279
rs529038750	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91413611	TTGAAACTTGACACT[C/G]TATATACTGAATCAA	143279
rs529086360	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91463996	TTTTGAATTTAAGTC[A/G]TTTTTTGCAAACTAA	143279
rs529093476	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91413003	AATTGTCATCAATAA[A/C]TTTTTCTTTGAGACA	143279
rs529117915	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91472375	ATAACCTAGGAAATA[C/T]CATTCTGGACATAGG	143279
rs529180904	snp	A/G	0.00993419	0.0697739	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91480285	GATTATAAAGCTCTA[A/G]GTAGGATAGGAAAGG	143279
rs529188755	snp	C/T	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432732	GAACTCTGACATTTA[C/T]CTTGAGAGCAAGCTC	143279
rs529304135	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410086	ACTCTGCAAACAATA[C/T]GGCGGTCGGGCGTCG	143279
rs529304821	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91469961	TTTAAACCAACAACA[A/G]TCAAAAAAGACAAGA	143279
rs529343671	snp	A/G			upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409033	AGATACCCCGAAATC[A/G]TATTTGGGTTTGTTT	143279
rs529365103	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477990	TTTGTGCATGTTGTA[C/T]GCTACACATACCAGG	143279
rs529382693	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91469344	AAAAAATGTTAAAGG[A/C]AGCTACAGAGAAGGA	143279
rs529396724	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477217	ACCCCTGCGGGTCCA[A/G]TGCAGATGCCAAGTG	143279
rs529421988	snp	C/T	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91418756	GACTGTAAATTATAT[C/T]GTTGGCTCCAGGATG	143279
rs529437303	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509690	ACAGAAAACCAAATA[C/T]CACATATTCTTACTT	143279
rs529439734	snp	C/T	0.0166325	0.0896639	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91428038	GTCTTTAATCCATCT[C/T]CAATTAATTTTTGTA	143279
rs529494459	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439514	TTTGCAGTCAGGTAG[C/T]GTGATGTCTCCAGCT	143279
rs529498378	snp	A/G	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91508569	CAAATCAAAACCACA[A/G]TGAGATACCATCTCA	143279
rs529536801	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91474561	GTTATACAGAAGAGG[C/T]TGATTTTTATTTGCA	143279
rs529540428	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445463	AATAAGTAATGAAAA[A/G]GCAGTCTTAGAAGTA	143279
rs529555859	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91455022	GTGAATAGTGCCGCA[A/G]TAAACATACGTGTGC	143279
rs529584631	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437691	TTATACTGTGTTTAA[C/G]GTAGAAATTCATAAT	143279
rs529645095	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91407469	AATAATTTCCCCAAG[G/T]TTACTTTAGGACAAC	143279
rs529687233	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91414156	AAAAGAGAGGTTCTA[C/T]ATGGGGTAGAACCCT	143279
rs529746021	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483836	CATTTAATAGAAGTC[A/G]TTGATTCATTATCAT	143279
rs529756800	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91473722	GTAGATATATTTTCT[C/T]GTGATTTTCTTAATA	143279
rs529829916	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502323	AAGTTGTTCCCTTTA[C/T]ATGTGATGTGCCAGC	143279
rs529849460	snp	A/G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91423751	TCTTTGGGCTCTTTT[A/G/T]TATTAATTTCTTTAA	143279
rs529866833	snp	C/T	0.0119091	0.0762411	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503855	AAAGACAGCAGTAAC[C/T]TCTGCAGACTTAAAT	143279
rs529868894	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500745	TTAGAGAGTCCCACA[A/G]TCTTATTTTATCTCT	143279
rs529894805	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440118	TTCCAATAATATGTT[C/G]AATAAGAGTAGTGAG	143279
rs529976014	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451019	TTACTGGGTTTTATC[C/G]TTTTACCACCCAAAG	143279
rs530013983	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502257	CTTTAGTCAACAGGC[C/T]GTTTGCTGGTTCCTT	143279
rs530024267	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450224	GAAATAATGCCACAC[A/T]TCTACAGTAATCTGA	143279
rs530033040	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458106	GGTTGAAGAATACAC[A/G]ATAAACATACAAAAA	143279
rs530076309	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91513050	AGCTTTTACAAATCA[A/G]TAAAGATGATTGTAC	143279
rs530087772	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449817	TAGCAATACAACTTA[C/G]AAAGTATGTGAAGGA	143279
rs530093147	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91456867	AATCAGTGAAACTGA[A/C]AACAGAAAAATTGAG	143279
rs530155882	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464885	TGTTAAAAAATTAAA[A/T]ATACAGATATGAGGG	143279
rs530211207	snp	A/C	0.00914312	0.0669923	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444186	GGCTATAAACACCTA[A/C]AATTAAATACAAACA	143279
rs530286822	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421020	TAGATCTTCCCTCAA[A/T]CCTTTGCATTCTTCC	143279
rs530315620	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422994	AGTTTCCCTAAAGTA[C/T]ACTTAGTTGTTCTGC	143279
rs530323466	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493739	TATCTCAAAATAAAA[A/G]TGGTTCTTTCCTATT	143279
rs530343401	snp	C/T			upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410206	CGGGGGAGGCGAGAG[C/T]AAGAAACCTGTGGGA	143279
rs530359053	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492675	TGATCAGTTGATTCT[C/T]TTACTGGGAATCCTA	143279
rs530390015	snp	A/G	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431287	TTTGTGGGTAACCCA[A/G]CCTTTCTCTCTGGCT	143279
rs530399159	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91506773	TCCCTAACTCATTTT[A/C]TGAGGCCAACATCAT	143279
rs530403423	snp	G/T	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445219	GGCCACATGATTAGG[G/T]GATTGATAACTGTTC	143279
rs530455858	snp	G/T	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502933	AAGCTGACTATCAAA[G/T]ACATACAACATTTCA	143279
rs530463564	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444404	GAGGATTATAGGGTA[A/C]GTTTAGAAACCAGAA	143279
rs530477555	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91453422	AGTGAAAGAGCAAGA[A/C]CCTGTCACACACACA	143279
rs530504174	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91435549	CATTGCTAAATTTCA[C/G]GCCACTCAGTTCCAG	143279
rs530511871	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477319	AATATAGTTGTCTTG[A/T]AGTGTAGAGAAGTAA	143279
rs530535213	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460703	CAAAAGACTATATGT[C/T]TCAAGTTGAAGGTGA	143279
rs530538760	snp	A/T	0.0023933	0.0345097	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91505906	AATGTAAAAGAACAG[A/T]CACTATAACAAACTA	143279
rs530629551	snp	C/T	0.0652144	0.168387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91428197	GTTGTAGATATGTGG[C/T]GTTATTTCTGAGGGC	143279
rs530681054	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91436203	ATCAGAAGTTTGGTA[A/G]TCTTTGATTTTCTGC	143279
rs530691749	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91514592	TAAAGCATTACACAG[C/T]ATTTATCAGTATTTT	143279
rs530748242	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499542	AGCTGCTTCCTGCTA[C/T]CTCAGGGCTCCCTCA	143279
rs530803062	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91416865	TTCCCACCACCCCAC[C/T]ACTCCCCAGAATTAA	143279
rs530813478	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426097	TTACATCATTATAGG[C/T]AGAATATGAATCCAA	143279
rs530822365	snp	A/C	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433788	TTTCCAGGACCTAGC[A/C]TTCGTGGTGCATGTA	143279
rs530871506	in-del	-/ATTTTAA	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492632	AGGACTGTTATTTAC[-/ATTTTAA]AAACTTGTTTGACCG	143279
rs530918182	in-del	-/TT	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433967	TTCACTAAAGATAAC[-/TT]TATAGAGAGGGGACT	143279
rs530959188	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409861	ACCAGCCCAGACCCC[A/G]AGGGCGCTTGCCCGC	143279
rs531061722	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91413807	GCAGTGGTTCCAGTT[A/G]GAGATTCTCAAGAGG	143279
rs531068458	snp	C/T	0.000132231	0.00813008	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496345	CATCTGCAATGTTAC[C/T]GTGGACGACTTATGT	143279
rs531118026	in-del	-/AAA	0.00398564	0.0444627	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509291	AAAAAAAATAAATTT[-/AAA]AAAAAAATCAAAAAA	143279
rs531122700	snp	A/T	0.00146214	0.0269987	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410552	GCTGCCGCCCATCGT[A/T]TCGGCGGGCGCCGGC	143279
rs531150246	snp	A/G	0.0023933	0.0345097	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409266	GAGAAAAAGGAAAAG[A/G]AGGGGGCGACAAGAA	143279
rs531163822	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91459937	AGTGTGTAGTAGGCT[A/G]TACCATCTAGGTTTG	143279
rs531205635	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91413098	TCAATTCGTGACCCT[A/G]CAATAGTGGCTTTTT	143279
rs531207695	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421246	ACTCTTCATTATTTA[A/C]CATTATTGACCTTTT	143279
rs531209151	in-del	-/T	0.00119737	0.0244387	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91513573	GTCAGACAGTAAATG[-/T]TTTTTTTTAATTTAC	143279
rs531235114	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476601	ATGCCACCACCGCAG[A/G]CATCCGGGGAGGAGT	143279
rs531297802	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471622	CAGCAAAGTTTCTGA[A/T]TGCAAAATCAATATA	143279
rs531309197	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492015	ACACCCAGCCCTAGC[G/T]ATGTGATTTTTTAAA	143279
rs531336925	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431145	CACTTAGGAAGCTTA[A/G]TTTGGCTGGATATGA	143279
rs531410981	snp	A/G	0.00318978	0.0398085	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91480505	GATATCTGTGAGAAT[A/G]TACCAAATAGATCTT	143279
rs531434189	snp	A/G/T	1.69573e-05	0.00291177	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492536	TTCATAATTGTTAGA[A/G/T]TGAAGTAGTCACCCT	143279
rs531537107	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91413762	ACAGTAGAAATCAGG[C/T]GTGGTGGGGAATTGA	143279
rs531544155	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484803	TATTTTCTACTTTGA[C/T]AATAGATTTCATAAT	143279
rs531640115	snp	C/G	0.00438332	0.0466095	intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462470	TATTTAATTATATTG[C/G]AATTACACTGAATCT	143279
rs531694671	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91479082	AGCCAGATGTGGTTG[C/T]ACCGTCCTGTAATTC	143279
rs531752015	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91411871	ATTTTATATAGGAAG[C/T]CTTTAACTCACAGAA	143279
rs531758672	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431291	TGGGTAACCCAACCT[C/T]TCTCTCTGGCTTCCC	143279
rs531763984	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91466541	TATATTCATTCAGTG[A/C]TATACATTTCCCTCT	143279
rs531783570	snp	A/C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470821	AAAAAAGCCCAGAAC[A/C/G]AAGTGGATTCACGGC	143279
rs531789688	snp	C/T	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437849	GAGTCTTTTCCATTT[C/T]GTTCTTGAATAGTTG	143279
rs531837436	snp	C/T	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91469991	AGCATTACATAATGG[C/T]ATAGAGTTCAGTTCA	143279
rs531843393	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501653	ATTTAAATGTGAAAT[A/G]TGTTTTTTATTTTTA	143279
rs531868188	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91411016	TTTTCTTTCCCTTCC[C/G]CCTTCAGATTAAACA	143279
rs531904956	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496744	CCAGCCTAGATTTGT[A/G]TGAAAATTTGTGGTT	143279
rs531928571	snp	C/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509734	AAATACTGAGTACAT[C/G]TGAACACAAGGAAGG	143279
rs531941863	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91475131	AGTGTTTTCGGCAGG[G/T]ATCATTTATAGTTAA	143279
rs531945631	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500430	TTGTGATTTGATCCA[G/T]TGAAAATAGTTCCAG	143279
rs531981279	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449181	AAGCTCATCTACCAC[A/G]TGAGAGAACTTACCC	143279
rs531993943	snp	A/G	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445988	CCGAACTTGCTGCAG[A/G]AATTTTTTTTTTTAT	143279
rs531997866	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91455973	CTGTTTTGGTTACTG[C/T]AGCCTTGTAGTATAG	143279
rs532058400	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500185	GAGATACTAGGATAC[A/G]GGATATTAGGTGGAT	143279
rs532065095	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467513	CAGCCTCGCCACACT[C/T]ACTTGCAGTGCACCC	143279
rs532081125	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91475809	ACAGCATAGTGCCCA[A/G]GGGAGAATCTAGAGA	143279
rs532081189	snp	A/C	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467012	AAGACTGGCACACTC[A/C]AAGCAGATCTTCAGA	143279
rs532098899	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458249	GAATATGTATGCTTA[A/G]AATCATACCATGCTG	143279
rs532116159	snp	A/G	0.00279162	0.0372561	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476053	TTGGCCTCTGAGGGC[A/G]TAGAGCAAAGTGGAG	143279
rs532159028	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458797	AGAAAAAAAATGAAA[C/T]GATCTTTGGGCTCTA	143279
rs532169582	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91408489	TATTTGTTCTATCAA[C/T]CTAGACTTAGCACAG	143279
rs532219137	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91429970	TTTTAACTGTGATGT[C/T]AGGGTGTCAATTTTG	143279
rs532256434	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452686	GGACTTTGCAGAGTC[C/G]CTGTTAGCAAGAAGG	143279
rs532257103	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452396	AGCAGCCAGGAAAAA[A/G]TGACACATTAAAGAA	143279
rs532263781	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91504557	ATGAATGAAATGAAG[C/T]GAGAAGGAAAGTTTA	143279
rs532279649	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91407619	ACATTAGTATTACTA[C/T]ACATAATTAAAATAG	143279
rs532281573	snp	C/T	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91416568	GCTGTACTATCTAGA[C/T]TTGTATAAGTACACT	143279
rs532285233	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497390	CCACCTCCCAGGTCC[A/G]AGCAATTCTCCTGCC	143279
rs532292620	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482438	TATGTGTTTCTCCCC[C/T]TGTTCTTTGTGATAT	143279
rs532300077	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499965	AGTTAAGTTTTGTTT[A/G]TGACACTCTGGTAAT	143279
rs532308379	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91486412	GAATTATTATGCATA[A/T]TTCACTGACAACAAC	143279
rs532325757	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433900	TGGAATGTCAAACCC[A/C]TCTCAAGGCTGTAAT	143279
rs532347428	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439907	TTGGTGTATAGGAAT[A/G]CTTGTGATTTTTGCA	143279
rs532379948	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431824	TTTGCCTTTGGTTTG[A/G]ATTTCCTCCTGTAGC	143279
rs532391496	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91443624	GTGCTGGGAGATCCT[C/T]CTGCTCTCTTCACAG	143279
rs532403766	snp	C/T	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440556	TTTTTGTTGTGTCTC[C/T]GCCAGGTTTTGGTAT	143279
rs532409266	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439382	GTCAAAGATCAGATT[A/G]TTGTAGATGTGTGGC	143279
rs532420962	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450297	CCCTATTTAATAAAT[A/G]GTGCTGGGGAAACTG	143279
rs532422836	in-del	-/T	0.00716266	0.059414	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483800	TTTGCTTTATGAGTG[-/T]TTTTTTTTAAAGACA	143279
rs532454295	snp	A/G	0.00318978	0.0398085	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451485	GTAACAAACCTGCAC[A/G]TTCTGCACATGTATT	143279
rs532510414	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460080	CATTAAAAACATTGA[A/G]CCTCATTGAAATACC	143279
rs532524275	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503486	CAAGGGGTCAGGGAG[A/T]TCCCTTTCCTAATCA	143279
rs532544898	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491833	CTGATTCCGCTATGT[G/T]ATTTATTTATTTATT	143279
rs532621499	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91495994	TCATTGAATACTATC[A/T]ACTAAACCACTCCTT	143279
rs532704320	snp	A/G	1.66749e-05	0.00288741	synonymous-codon, intron-variant, nc-transcript-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483023	TCACTTGCTACGACA[A/G]ATAGCTACCTTAGTG	143279
rs532716785	snp	A/G			intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481907	ATATGTCTAATGAAA[A/G]AACATATACAGGGTA	143279
rs532742410	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91423802	CACCTATGCACAAGA[C/T]TCACTGTATGACAAG	143279
rs532790856	snp	C/T			intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91407342	TTAGGATTACAGGCA[C/T]GAGCCACCACACCCA	143279
rs532804495	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91436358	GTCTTTAGTTATTTC[C/T]TCTTAGCCTAATCAG	143279
rs532816710	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484083	AGAGAGAGTATTGAG[C/T]TAAAACAAGGCAGAA	143279
rs532818159	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445267	ATGGCAACAGCAGTA[C/T]TGGAGGTAAAGAAGA	143279
rs532876467	snp	A/G	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91494868	ACAATTTAGATTTGG[A/G]TGATATTTTGACTCT	143279
rs532900426	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91454287	GGGCCATAAAACAAC[G/T]GAAATTTTGAAGAAT	143279
rs532922014	snp	A/C	0.0134861	0.0810011	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91428538	TCCATTTGTTTATAT[A/C]CTCTTTTATTTCATT	143279
rs532987142	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420382	TGAGGTCAGGAATTC[A/C]AGACCAGCCTGATCA	143279
rs533044549	snp	A/G	0.00279162	0.0372561	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91429307	GAGGATTTTTGCATC[A/G]ATGTTCATCAAGGAT	143279
rs533050150	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499632	TCAGTTTGGTCTGAC[G/T]TGTCTTAGCCATGTG	143279
rs533076516	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91479289	TGGTGACTGGATTTG[C/T]TTGGACACTACTATT	143279
rs533085915	snp	A/G	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91507275	GGAAGTTCTGGCCAG[A/G]GCAATTAGACAGGAG	143279
rs533086115	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476117	TGCGTTGTTATACTG[A/C]TAGGAATGTTTTAGT	143279
rs533156522	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412077	TGCTTTGGGATTTCA[A/G]GTTTTTCAGATTTTA	143279
rs533222259	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419493	GTGATTATATCATCA[A/G]AAAGACCATTGAAGC	143279
rs533265994	snp	C/G	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487390	ATGTTGTTCACAGGT[C/G]ATGATATACAATGAA	143279
rs533267334	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478189	TACCTTACTGTTTTC[C/T]TTTGCCTACAGCCTC	143279
rs533328155	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477125	AGCGGAGCTTGCAGT[C/G]AGCCGAGATTGCGCC	143279
rs533388561	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461464	TTAAACATGCATATA[C/T]TATGTATTGATTTCA	143279
rs533449159	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503715	AGGGGCGCCCACCAT[G/T]GCCCAGGCTTGCTTA	143279
rs533464661	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476626	AGGAGTGCCAAACGG[A/G]ACTTGGCCAGGAAGG	143279
rs533479979	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409935	TGTGCCTACGTCCTG[C/T]CCTACTGGTACCACT	143279
rs533480366	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91486634	ATTCACAAAGTATCA[C/T]TTCTCTTGTGCATAA	143279
rs533601524	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91453589	ACTATATATAAATCA[A/C]AAGAGAATTCTAAAA	143279
rs533667678	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460840	GTGGTAATTAAATAA[C/T]AGACTGTTACCATTT	143279
rs533721815	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431449	TAGATTGGGGAAGTT[C/G]TCCTGGATAATATCC	143279
rs533738090	snp	A/G	3.47518e-05	0.0041683	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493406	ATAATAACATTATTC[A/G]TGTGTTTTTTTAGGC	143279
rs533797727	in-del	-/TC	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91465966	GGACTTAGAAAGTAT[-/TC]TCTCTGCTTCTGTTT	143279
rs533867808	snp	A/G			intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482004	GAAGAGAAATGTAAG[A/G]AGGGAAAATAGAGAA	143279
rs533871990	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464467	ATAAGATAATTATCC[C/T]TTATCTCACTATGTT	143279
rs533881849	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91463125	ATCTGTGTATAACTT[C/T]TGACTCCCCAGAAGC	143279
rs533882004	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471688	AGCAGAGAGCCAAAT[C/G]AAGAACGCAATTCCA	143279
rs533919138	snp	C/T	0.00478085	0.0486577	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91413292	CTGGAAAGGGCAGCC[C/T]TGAAGTGTTTTATCC	143279
rs533937834	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509910	TAACAAACCTGCACA[C/T]GTACCCCTGAACCTA	143279
rs533995495	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445793	AGGGATCAGAGAAAT[C/G]CCTCCCCTAGCCAAG	143279
rs534049731	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450041	TACTTTACATTTCAT[A/G]TAGAACCAAAAAAGA	143279
rs534051929	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91459462	TAACCATATAGCGGT[A/G]CACCCAAATAGTGGA	143279
rs534057663	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91454647	CATATGTATACATGT[A/G]CCATGTTGGTGTGCT	143279
rs534070549	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509101	GACACAGGAAGGGGA[A/G]CATCACACTCTGGGG	143279
rs534123935	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412507	GTCGCCAGGCTGAAG[A/T]GCAGTAGCCTGATCT	143279
rs534136948	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420601	TCAAAAGAAAAAAAA[A/G]AAAAGAAAAAAAGAA	143279
rs534138410	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512694	CACTGGGAAAGCAAA[A/G]TACAGTGAAGAATGA	143279
rs534179348	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91429051	TTTTGAAATGTGTCC[C/T]ATCAATACCTAATTT	143279
rs534210187	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91479665	AAATCTTCTTTTCTG[A/G]GCATTTATGTAAAAA	143279
rs534244275	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91446312	ACTAACAAACAGAAA[C/G]GAATAGCATCAACAT	143279
rs534254078	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490763	GGGCGTGGTGGTGGG[C/T]GCCTGTAGTCCCAGC	143279
rs534278574	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485061	TTGGAGCTACATTTA[C/T]TTAAAATAGGAGTTT	143279
rs534288147	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496573	TCCTAAGCTTTTACA[A/C]GATAGAGAGGCAGTA	143279
rs534294178	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438041	CATTCCCCTCAGGTA[C/G]ACCTTGAAGTTCTTT	143279
rs534307843	snp	C/T	0.00795532	0.062565	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91416327	AAACCTTGTACAAAG[C/T]ACTCAGTGTTAGATG	143279
rs534362128	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471090	AAAATACTAGCAAAC[C/T]GAATCTAAAAGCACA	143279
rs534365459	snp	G/T	0.0166325	0.0896639	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440766	CAGAACTTGTTATTG[G/T]TCTATTCAGAGATTC	143279
rs534398120	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421525	CACAAAAAAAATTTA[C/T]AATGTTTTAAGAAAG	143279
rs534399824	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91434719	TATACATAGTATAAG[A/G]TTTGGCATTGTTCAA	143279
rs534457443	snp	C/T	0.0119091	0.0762411	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503647	ACGGAGTCTCGCTGA[C/T]GGCTAGCGCAGCAGT	143279
rs534487811	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476753	AAGGGCGAGAGGAGT[A/G]AGAACCGTCTTCTTG	143279
rs534510064	snp	A/C	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91417936	GATCCCTGAGGAATC[A/C]CCACACTGACTTCCA	143279
rs534585172	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91424565	ATAGTTTAATCTTGC[A/G]CTTCAAAGTATGTGT	143279
rs534597461	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91486707	AACTAATATATATCT[C/T]ACTGAGTTCATTGCA	143279
rs534671348	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476429	GGAAACAATCATGAC[A/G]CGGACCCCCACGAAG	143279
rs534676221	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440255	GAAACATCCCATCAA[C/T]ACCTAGTTTATTGAG	143279
rs534687535	in-del	-/TTAAG	0.00795532	0.062565	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512503	ACCAACTTTAAAATA[-/TTAAG]TTAAGTTTTTAAAAA	143279
rs534739714	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451121	GACTGGGAACCAACC[C/G]AAATGCCCGTCAATG	143279
rs534747027	in-del	-/TGTT	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91436149	CACGTTGCTTTTGTC[-/TGTT]TGTTTTGGTCTCTGT	143279
rs534779811	snp	A/C	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467838	GCACCCAATCATGCC[A/C]CCATTGCTGCTGCAA	143279
rs534789549	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91473393	AGGGTGACTTAAAGA[A/T]ATTTAAAATAAACAA	143279
rs534807145	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91408858	TTAAAGTAGAAAGCC[C/T]TTCTATAAATGAAAG	143279
rs534820227	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91417230	AGCTATATGAATAAC[C/T]ACTTACTCTTAAGTT	143279
rs534838051	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503009	CAGCTGAAAGAGGAG[A/T]TTCCATTCATCTTAT	143279
rs534850767	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482178	TACCAGATGAAGTTA[C/T]CAGCTGAGGTCAGTC	143279
rs534927242	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91514080	CTCTCTTACACTGCT[C/T]GAACTAGAAAATCAG	143279
rs534942748	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450625	GTTTGCAATCTATCC[A/G]TCTGACAAAGGGCTA	143279
rs534949777	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485988	ATTTAATACACTGCA[C/T]TTTATATCCACACTT	143279
rs534980281	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467164	AGGGTGAGTTGAACA[A/G]GCAAGGAGCAGCCTG	143279
rs534988749	snp	A/C	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91474011	TGTGTAATTAAGAAG[A/C]AAAAGCCAAAAGATG	143279
rs535024714	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91423296	TGGGCATGGAAATTC[A/G]ATTTCCCCATCTATA	143279
rs535049851	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468417	AAATAAAATCCCATT[C/T]GAAGGGTAGCAACTC	143279
rs535074159	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470226	TGGACCTAACAGATA[C/T]CTGCAGAACTCTCCA	143279
rs535095126	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91411338	GTGGTTGTGACTGGT[G/T]AATTTGAAGCACAAT	143279
rs535100453	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483116	ACTTTTATAGTCTCA[C/T]AGTTTTAAGTTTGGT	143279
rs535151036	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91428652	CAATTGTGAATGGGA[A/G]TTCACTCATGATTTG	143279
rs535152114	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91494190	AAGCACTGGAGATAA[A/G]AAAGTATAAAAGGGG	143279
rs535156923	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464653	GTATTTCTCTTTACT[A/G]TTGGGGATTCTGGTA	143279
rs535300924	snp	G/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91455385	CTTTTGAGAAGTGTC[G/T]GTTCATATCCTTCAC	143279
rs535317265	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497355	GAATGCAGTGGAACA[A/G]TCTCAGCTCACTGCA	143279
rs535366457	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461937	TTAAAATAATCTTTG[C/T]ACATTTCTTTTTATT	143279
rs535395846	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431999	AGACTTCCTTTATCT[G/T]ATTAGAACTCCTGGT	143279
rs535507533	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419070	GCTTTTAAAGCATTT[C/T]GTGATGGAACAGCCA	143279
rs535576383	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91489374	CAAGGACAATCTTAC[A/G]AATAGTCAGTGTAAG	143279
rs535638320	snp	C/G	0.0111196	0.0737302	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91427767	TTTGTCAGATGAGTA[C/G]GTTGCGAAAATTTTC	143279
rs535820015	snp	C/G	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91506248	CACATTCAAAAGCTA[C/G]CAGAAGGCAAGAAAT	143279
rs535822931	snp	A/G	0.0023933	0.0345097	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91504985	ATTCAACATTCTTAA[A/G]GAATTTTCAACCCAG	143279
rs535856054	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502521	TTGTATGCTCCAAGT[A/G]ATCACACATGGTAAG	143279
rs535875579	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452987	AGAAGGAAACTTGAG[A/G]TGTGAGGAAAGGGGA	143279
rs535882799	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461011	GAAGGGAAGGAAGGA[G/T]CGATAATTGAGCGAC	143279
rs535962106	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91459428	CCTAAAAACAGATGT[C/T]CTTCAGTGGTTGAAT	143279
rs535972183	snp	C/T			intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91407967	ACAACACTCTCTTCT[C/T]CCACCTGGGTCTCCA	143279
rs536027862	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499703	ATCATAGGATACCTT[C/T]CAGTCACCCCAGCTA	143279
rs536045983	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432690	AAAAATCTTTCCAGC[C/G]TAGGTAGTTCAGAAA	143279
rs536171723	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439068	TTTGCTGTGCAGGAG[A/C]TGTTTAGTTTAATTA	143279
rs536201259	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497960	TCTTAGCCTCTGGAT[A/G]GTAGAAATCATTAAC	143279
rs536216195	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491901	GAGTGTAGTGGTACA[A/G]TCAAAGCTCACTGCC	143279
rs536230565	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91513742	ATGGTTCATATGCAA[A/G]TAATACTTTCCCCAA	143279
rs536256555	snp	C/T	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490822	CATGAACCCAAGAGG[C/T]GGAGCTTGCAGTGAG	143279
rs536307139	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477069	GCCTGTAGTCCCAGC[C/T]ACTCGGGAGGCTGAG	143279
rs536310630	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437414	CTCAAAAGAGAGAGC[C/T]AAGCACAAATGTTAT	143279
rs536344147	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457093	ACCAATTCCTCAAAA[A/C]ACAAAAGCTATTGCA	143279
rs536369611	snp	A/T	0.00716266	0.059414	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91448831	GACTAAACCAGGAAG[A/T]AGTCGAATCTCTGAA	143279
rs536377031	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419247	ATGATGGAAAACCAT[A/G]GTTGTTATTCTTATT	143279
rs536405319	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91480367	AAACACTTGTCAGCA[C/T]AGAGAATGACAAAAG	143279
rs536441859	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91455479	GGATATGAGCCATTT[G/T]TCAGATGAGTAGATT	143279
rs536448547	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91413334	AAACGTGAAGGAAGT[C/T]CATTCCAGCTAGTGA	143279
rs536460100	snp	A/G	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91494371	TGGTGAGAGTGGTGG[A/G]ACATTATAAGCTGAG	143279
rs536565641	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450446	AACCTAGGCAGTACC[A/G]TTCAGGACATAGGCG	143279
rs536589368	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91480880	TATAGCCTAGTTAGC[G/T]CAGTCTTTAGTTATC	143279
rs536596295	snp	C/T			intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91515041	ACACCCAGAAGTGAA[C/T]CAAGTGTAACATTTC	143279
rs536596605	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503242	TCAGAATGGCTATTG[C/T]TATATTAAAAAGTCA	143279
rs536623798	snp	A/G	0.00993419	0.0697739	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91486777	TCAAAATAATTATAT[A/G]CCAGTACTGAAGAAC	143279
rs536635294	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91430748	TAGATCTTCCTCCCT[C/T]CTTTTATTTTGAGCC	143279
rs536658129	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497667	AGGGGAGGGCACTGT[A/G]CATGTATGAACTGTA	143279
rs536658943	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91486070	TCATGAGATGTTCAG[A/G]AGATTGCATTTAATT	143279
rs536659086	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501429	ATGTGTACTCCGTTT[A/G]AAGTTATTTTCATAG	143279
rs536688749	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91434255	TAAAAACCACTTGTT[A/G]TGACTAATCCATTCT	143279
rs536692766	snp	A/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91430065	ATGTGTCCCAGAGAT[A/T]CTGGTATGTTGTATC	143279
rs536711824	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449409	TCAAAATAATAAGAA[C/T]TATTTATGACAAACC	143279
rs536797666	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91511355	CATCAAGGGGCATCT[A/G]CTGTCCCCAAAATGC	143279
rs536926410	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477304	AATAAGAAGGTTTGA[A/C]ATATAGTTGTCTTGA	143279
rs536988341	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476809	TGTGAGCACCTGTGA[C/G]GCCTTTGTCTTTGGC	143279
rs537017674	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445904	ACAGACAAGGAGATT[A/C]TCTTGGGTGCCTATG	143279
rs537018783	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426488	GACCTATTCTACATT[C/G]TTATAGGTTAGTATT	143279
rs537102849	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433517	TCTTTATTATTTTTT[A/T]CAAATATATTCCATT	143279
rs537140173	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439872	GTTCACTGATGATTT[G/T]GCTCTCTGTTTGTCT	143279
rs537162760	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91443263	TGACCTTTGGATGGG[A/G]TTTTTGTGTGGACAT	143279
rs537188614	snp	A/G	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91474231	GAAGCATTAAAAAGT[A/G]AGTTGAATGAAAACA	143279
rs537199377	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496652	TTATTTAACCCTTCA[A/G]TTTAGTTTCTTTATG	143279
rs537212342	snp	G/T	3.35554e-05	0.00409592	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460411	ATTATTTTGAATGTG[G/T]TTTTATACTTCACAG	143279
rs537244224	snp	C/T	0.00279162	0.0372561	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91418853	ATTTTAACTTGAAAC[C/T]TATAAATATATGTTT	143279
rs537305380	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91418001	TGTAAAAGTGTTCCT[A/G]TTTCTCCACATCCTC	143279
rs537322302	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91511259	ATAGCTGTAAGAATC[C/G]TAAATGATGATAACA	143279
rs537336085	snp	C/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451238	GACATGGACGAAGCT[C/G]GAAAGCATTATTCTC	143279
rs537347748	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467647	ACCTGCAACATCCCC[A/C]CATCAGAACCTCCCC	143279
rs537354304	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458403	GTCAAAATTCCTGTA[G/T]GTTTTTTGTTGTTGA	143279
rs537408424	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462913	AATGTTTTGTAGTTT[C/T]CTGGATAGAGGTGTT	143279
rs537458415	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412354	TACTACTAGACAAAG[A/G]GAAGAATATATTCAA	143279
rs537532882	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91475156	AGTTAAGAAAGATCT[C/G]TCTAGATGCTTAGCA	143279
rs537553322	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426250	ATATTGTTTTATCAC[A/G]GGAAATGTACATTAC	143279
rs537607557	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501676	TATTTTTAGGAAAAT[C/G]ATTAAGTTGGGATAT	143279
rs537699398	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91515248	GAAAAAAGACCAGGA[C/T]GGGTTTTCGCAGGAG	143279
rs537706360	snp	G/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91513774	ATCTTTCTGGGCTAG[G/T]CTATTTTCTTGCTAT	143279
rs537740958	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449060	GATACCAAAACCTGG[C/T]GGAGACACAACAAAA	143279
rs537752657	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91455475	TTCTGGATATGAGCC[A/C]TTTGTCAGATGAGTA	143279
rs537754900	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91411927	TTGTTTAAAACAGTA[A/T]ATGTATGTACTTATA	143279
rs537834328	snp	A/T	0.00478085	0.0486577	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91508951	ATGCAGCCATAAAAA[A/T]TGATGAGTTCATGTC	143279
rs537850560	snp	G/T	0.00438332	0.0466095	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91506295	GAACTGAAGGAAATA[G/T]AGACACAGAAAACCC	143279
rs537914972	snp	A/C	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471021	ACACACGCACACACA[A/C]AAAGAAAACCTCAGG	143279
rs537946328	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426767	AATATGGTCCACTTA[C/T]TTGAGCTTCCATCAA	143279
rs538041216	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91511441	TATTATCTACTCCTC[A/G]GCTGCTAGATGTTTT	143279
rs538094763	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91428893	CTGTCTAATTGCCCT[A/G]GCCAGAACTTCCAAC	143279
rs538132499	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91456356	TGAATGGGAGTTCAC[G/T]CATGATTTGGCTCTC	143279
rs538142852	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464337	TGTGGCTTAAAAAAT[C/T]GCTGGTTGCTGTCAG	143279
rs538144661	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450784	GGCTCATCATCACTG[A/G]TCATTAGAAAAATGC	143279
rs538202611	snp	C/T	6.64905e-05	0.00576548	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499179	TTTAAATCAAGCTTT[C/T]GGTTAGCTTTTGTAG	143279
rs538221245	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91494447	AGAGCAGCAGCAAGC[A/G]CACTGAAAGTTATGG	143279
rs538233173	snp	G/T	0.00478085	0.0486577	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485951	ATAATAATTAATAGA[G/T]TTGTAAAACAGTCAC	143279
rs538248908	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91515071	CATTGGCCGTAGATA[C/G]ATAACTTCAGCTCTT	143279
rs538249222	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503270	TCAAAAAATGAGGGA[A/G]GAGCCAAGATGGCCG	143279
rs538340099	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422722	ATAATTTACTGACTA[C/T]TTTATGGAAAGGTAT	143279
rs538376276	snp	A/G	0.00438332	0.0466095	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91453906	ATATCAGATAAAGTG[A/G]ACTTAGAACAAAGAA	143279
rs538385830	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91513962	GTATATTATTTCAAG[C/G]GTATTTCTTCTTAAA	143279
rs538391789	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478493	AAGATCTGTGAATTC[G/T]TTTAAATTGTATGTA	143279
rs538412938	snp	C/T	0.00318978	0.0398085	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91429516	CTGGTCCTGGACTCT[C/T]TTTGGTTGGTAAGCT	143279
rs538434247	snp	C/T	3.35892e-05	0.00409798	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425278	TAACTTTTCTGTTTT[C/T]AGGGTTTGGACAGAG	143279
rs538515428	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492960	GTATAATCCTTACTA[G/T]CTGTTAAACTTTTCA	143279
rs538547917	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91435805	CTTGAATTATTTTGT[C/T]GATGATTTTCTCTCC	143279
rs538575033	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432152	AAATGTAAGCATGTT[G/T]ATAGTTTCTTGATGT	143279
rs538667568	snp	C/T	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439611	TAGTTTTTTCTAATT[C/T]TGTGAAGAAAGTCAA	143279
rs538667583	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451074	GACACATGCACACAT[A/G]TGTTTATGACAGCAC	143279
rs538683882	snp	A/G	0.00557542	0.0525036	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91424262	CTGTTAGAATGAATC[A/G]GATGGCTCTACCTAA	143279
rs538702742	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438848	GATGAGCTTTTTTTC[A/G]TATGTTTGTTGGCTA	143279
rs538733370	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419763	TTTGTACTTATCTTC[A/G]ATCTGGAACAGCTGG	143279
rs538743959	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457773	CTCTCAGCACTCTTA[G/T]TCAACATGGTAAGAA	143279
rs538782662	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491977	AGCCTCCCAAATAGT[C/T]GGGATTACCAGCTCA	143279
rs538809052	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91411136	CATATGGTACAGACA[C/T]GTGACTCAGGTGGGG	143279
rs538809189	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91475378	TGAGTGGATGCTGTT[C/G]CCATTTAATTAGATG	143279
rs538868940	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91424381	GTGAATTAAGAAGGA[A/G]GAGATGAAAAAGAAA	143279
rs538897079	snp	C/G	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457137	GAAATAGTTAATTTG[C/G]CTCGTTTTATAACCA	143279
rs538910390	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484950	CCATCTGCATATTCC[C/G]TTTAATACTATTATA	143279
rs538919625	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445745	GGGGGCAAGCTGAAG[C/G]AAGGTGAGGCTTTGC	143279
rs538922956	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91473803	ATATAAAATATGTGT[C/T]AATAAACTATATTAT	143279
rs538941091	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484073	ACACTTGCAAAGAGA[C/G]AGTATTGAGCTAAAA	143279
rs538958237	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91473136	AGGGGAAACAAAATA[C/T]ATACTAAGCAAGATA	143279
rs538971274	in-del	-/AATT	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91479437	TCATCTTTTAAAAAC[-/AATT]AAAATCATACTGTAT	143279
rs539001871	snp	C/T	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422334	TCAATGAAAAAATGC[C/T]TTCTATGTGTTAAAT	143279
rs539043312	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91418907	AACCTTTGCTCAGTA[A/T]CTCAGGAAGCTACTC	143279
rs539065146	snp	G/T	0.0205511	0.0992634	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431303	CCTTTCTCTCTGGCT[G/T]CCCTTAACATTTTTT	143279
rs539149469	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502316	TGCTTTCAAGTTGTT[C/T]CCTTTACATGTGATG	143279
rs539150729	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91488143	CATTAGGCAAACCAC[G/T]CAAACTACTGAAACA	143279
rs539284928	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461799	GGTGATCCTCCCATG[C/T]CAGCCTCCCAAAGTT	143279
rs539346016	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470102	TACAAAGAGACTTAG[A/G]TAACCACACAATAAT	143279
rs539358407	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91469564	AATGCTAAGGAAATT[C/T]GTTACCACCAAACCT	143279
rs539383882	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461107	TCCAATTAAGAATTA[C/T]AAATCCATAAACTAT	143279
rs539499792	in-del	-/TG			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498788	AAGGGGGAAAAAAAC[-/TG]TTTTTTAAATTTTAC	143279
rs539518000	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91417088	ACAGAAGATGAATGA[A/G]GAAGTAGGTGGAGAT	143279
rs539518056	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91407879	GTTGCACGTCTGACA[C/T]TTGGCATAGCTAAAA	143279
rs539529333	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471298	AAAAACCCTCCACAA[C/G]TAGGCATTGAAGGAA	143279
rs539547936	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91486929	GACTATGCTCAGAGG[A/G]ATTCCAGCTGTAACT	143279
rs539549887	in-del	-/A	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490497	GAAAATTCAATATCT[-/A]AAAAATCCTAAGTCC	143279
rs539567723	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498788	AAGGGGGAAAAAAAC[C/T]GTTTTTTAAATTTTA	143279
rs539651687	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91411130	ATTTTTCATATGGTA[C/G]AGACATGTGACTCAG	143279
rs539701934	snp	A/G	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91443311	ATGCTATTCCTTTCT[A/G]TTTGTTAGTTTTCCT	143279
rs539704781	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452829	GGACTGTCAATGCAG[A/C]ATCCTATACCTGATG	143279
rs539747683	in-del	-/T			intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91463957	CTTCTCTGAACTTGA[-/T]TTTTTTTTTGACATT	143279
rs539766813	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460098	TCATTGAAATACCCC[C/T]GGAAAGATGACTTTT	143279
rs539855656	snp	A/T	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91459333	ACATGCAACTGCCGT[A/T]TATTTACCTCAAAGA	143279
rs539878758	snp	G/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437046	AGATAAGGAGTATGA[G/T]ATTCTGAGAGATTAC	143279
rs540005781	snp	A/G	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497757	CATTAGCAGATTTTC[A/G]TAGGAATATAAATTG	143279
rs540097286	snp	G/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91430393	GTAGATGTCTATTAG[G/T]TCCGCTTGGTGCAGA	143279
rs540136993	in-del	-/T	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491639	CTTTGTTCCTGGTTA[-/T]GTGTGTAACAAGTCA	143279
rs540146945	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452057	GGGATAGGAATCAAT[C/G]AACTGGAAGACAGAA	143279
rs540160210	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437668	TTTTGTTGTTTTCAG[A/G]TATTTTCTTATACTG	143279
rs540178607	snp	A/T	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91504279	AAAGCTGGACGGAGA[A/T]TGACTTTGACAAGCT	143279
rs540196891	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91455213	TGTTCCTATTTCTCT[A/G]CATCCTCTCCAGCAC	143279
rs540203130	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491372	ATGATTATTATAAAA[A/G]TCATAGTAAACTTTT	143279
rs540216041	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500969	AAAAATGGTTCCTGT[A/G]CTATCCACTGCTGAA	143279
rs540219576	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477872	TAATAAACATGTTAC[A/G]CTTGGATTCTTGTTC	143279
rs540244315	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91510729	TAAAAAACTGAGTTG[C/G]CATTTTCATTTTTTT	143279
rs540251702	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500248	GAGAAGAGTAATTTG[G/T]ATTTGTGCAAAGTAA	143279
rs540257100	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452577	GATTCATGGGTTATC[A/T]TGGGAATAGGACTGG	143279
rs540274015	in-del	-/GGCCCTGAGAAGGGAACACAATT	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91474962	GACAGCTAATAAAAA[-/GGCCCTGAGAAGGGAACACAATT]GGCAAATTCAGAAAT	143279
rs540315037	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91427871	GCTGTGCAGAAGCTC[G/T]TTAGTTTAATTAGAT	143279
rs540372002	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499310	AGTTCTCTCATTTCA[G/T]TCTTAATTCTTTAGA	143279
rs540379439	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481212	GTATGTGAAATGATA[C/T]TAAATATTAAATATC	143279
rs540405517	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421919	ACTTACACCTGAAAT[C/T]GCTGTTAACAATTTG	143279
rs540431748	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91411606	CTGTATTGGTGTTAG[A/G]AATAATTTTCGGATT	143279
rs540434378	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492115	AGGCAGTAGATACCA[A/G]GAGGTAGTACTTTGG	143279
rs540491461	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410913	GTTGGATGAGCATAG[A/G]TGTCAGCAGGCGGGA	143279
rs540631230	snp	C/T	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91435922	TTCTCTTCTCTTTTG[C/T]TTTATGATTTAGGGA	143279
rs540731332	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422932	AGGTGAAGGAAGGGG[A/G]AAGAAAAGAAAATGT	143279
rs540750746	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91435237	CCCTTTTTTATAGTT[C/T]CCTCTGTGTGAATGA	143279
rs540750755	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445029	GCTGTGGTAGGGGTT[A/G]GCAGTATATTCAAAA	143279
rs540792916	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439657	GATAGCATTGAATCT[A/G]TAAATTACTTTGGGC	143279
rs540798746	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482625	ATACATTTTCTTTTT[C/T]GATACTCAAAACAAC	143279
rs540912295	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461536	TATATAAGTATATGG[A/G]TTTTTTGAGGGGGTT	143279
rs540933798	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91416439	CTGTTTAGATATGTT[C/T]AGATGCATACTTAGT	143279
rs540938267	in-del	-/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91454905	GACATGAACTCATCC[-/T]TTTTTATGGCTGCAT	143279
rs540978236	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91474629	GCAGTTAGTCAGTGA[G/T]TATGTATTGTCTTGG	143279
rs540997955	snp	C/T	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91465719	TTTTTAGCTTGTCGA[C/T]GTGATGAATTACATT	143279
rs540998723	snp	A/G	0.00358779	0.0422022	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415434	AGCTACTTATTGAGT[A/G]CCTACTCTGTGCTAA	143279
rs541001099	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500908	CTTGTAAATAACAGT[G/T]TAATAGCACTATGTT	143279
rs541009544	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91475445	AAAAAGAAGAGTATT[C/T]CACCTTGTCAGATGT	143279
rs541038182	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91456839	GAAAGCAAGCAGGAA[C/G]GAGGAAATATAAAAT	143279
rs541039481	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483773	CATTTTTGTCAGCCA[A/G]TCAGTATATAACTTT	143279
rs541110148	snp	C/G	0.00358779	0.0422022	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464839	AGTCCTCTCTGAGTT[C/G]TTTTGACTTGGAATA	143279
rs541194215	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458646	ATGAAGGAAAAATAA[A/C]CTTTTCAATAAATGG	143279
rs541220004	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509018	TCTCAGTAAACTATC[A/G]CAATAACAAAAAACC	143279
rs541285390	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91407440	AATCTTTTTAACAAG[A/G]TCAACATGGCTAAAA	143279
rs541312071	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467397	GGAGACTTTAGCCTT[A/G]AGAAGACTGTCAGAC	143279
rs541333637	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457278	CTACCAGAAAATAGA[C/T]GAAAAGGGAACACTT	143279
rs541370731	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449789	ACAATTGCTGCAAAG[A/G]TAATAAAATACCTAG	143279
rs541390301	snp	A/G	3.31252e-05	0.00406958	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461232	TCTATATGTATATAC[A/G]GTTAATGTGTTTTCA	143279
rs541392237	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91453273	TTTGTCTCCATAAAA[A/T]ATTTAAAAATTAGTC	143279
rs541514364	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91436777	CTGCAGTATAAATCA[G/T]TTACTTTGTGATTTC	143279
rs541524038	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409842	TGGAAGAAGGCGAAA[A/G]GCCACCAGCCCAGAC	143279
rs541645404	snp	A/C	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499502	TAAAAGTTACAACTT[A/C]TTAATGATTAAGGAA	143279
rs541645566	in-del	-/A	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91495369	GAAGTATAAGGCCTT[-/A]ATTATCAGACTTCAT	143279
rs541646030	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439240	CTTTAATTCATCTTG[A/T]GTTAATTTTTGTATG	143279
rs541666782	snp	A/T	0	0	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91513026	ATTCAGGGTTTTAGA[A/T]GTGTACACAGCTTTT	143279
rs541708734	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450192	ATATAAACCAATGGA[A/T]CAGCATAGAGACCTC	143279
rs541748151	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445124	ACTGTTTTCACAGAC[A/G]TCACAACTCTCGTTG	143279
rs541755024	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490751	AAAAAATTAGCCGGG[C/T]GTGGTGGTGGGCGCC	143279
rs541810879	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410259	GGGCTGGCGCGCGCG[A/G]GGGCGGCCTCGGGCT	143279
rs541847204	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433028	TTGCTATTTGTGGAA[A/G]GCAAAGGACTTGCCA	143279
rs541877380	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91504433	AGAGAAGTGCTTAAA[A/G]GAGCTGATGGAGCTG	143279
rs541883735	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490728	AACCCCGTCTCTACT[A/T]AAAATACAAAAAATT	143279
rs541953918	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425164	ATTTATATACGTTTT[A/T]ATCTATTATCTACTC	143279
rs542012054	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476947	GCACTTTGGGAGGCC[A/G]AGGCGGGTGGATCAT	143279
rs542018906	snp	C/T	0.00358779	0.0422022	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468444	ACTCCAGAAACTGAA[C/T]GAATGTCAACTCACT	143279
rs542080115	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425891	TGTTATAACGATATA[A/G]CATAGGTAAAAAGAT	143279
rs542109235	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444338	TGGATTTTGGCAGAG[C/T]CTGAGAGTGGAGAGA	143279
rs542140853	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433687	TTCATCTGCAGGTTT[A/G]TCTATAGGATATTTC	143279
rs542203652	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470413	CCACTCAAAAGCATA[C/T]AATTATAAGGAAATT	143279
rs542227644	snp	C/T	0.00914312	0.0669923	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497120	ATGTGCCACCGTGCC[C/T]GGCAAATTTTTTTTT	143279
rs542251811	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91513243	ATAATCATTGATGAA[A/G]TATGTCAGTTACAAG	143279
rs542268339	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91506309	AGAGACACAGAAAAC[C/G]CTTCAATAAACTAAT	143279
rs542298404	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440378	AAGTGATAGGTTACA[C/T]TTATTGACTTGTGTA	143279
rs542309209	snp	C/T	0.0178098	0.0926698	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91427810	GGTTGCGAAAAATTT[C/T]TCCCATTTTGTAGGT	143279
rs542384127	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409218	CTCTCTTTTCTCCTA[G/T]ATCAGCAGGTGTCCC	143279
rs542399878	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91414314	GGGGAAGAGTTTGAG[C/G]GTGAGCATAAGGTGT	143279
rs542424854	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476566	GAACAGAGGCCAGAG[C/T]CCAGGCAGGATATGG	143279
rs542447479	snp	C/G	0.00517822	0.0506191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91417527	CCCTCCCCGCCCCCC[C/G]ACAACAGGCCCGGGT	143279
rs542452868	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422776	TTTTCAATTTTCTCT[C/T]TTATCTTTGAGACTG	143279
rs542472430	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91472432	TGCCAAAAGCAATTG[C/T]GACAAAAACAAAAAT	143279
rs542505371	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91413613	GAAACTTGACACTCT[A/G]TATACTGAATCAAAA	143279
rs542507369	snp	C/T	0.0023933	0.0345097	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431584	TTGTTCATTTCTTTT[C/T]ATTCTTTTTTCTCTA	143279
rs542614231	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91480471	GGTGAACCATTTTCA[A/G]TTGAAGAAGTTACTT	143279
rs542631996	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502103	TATCCTATTAAACTC[A/G]TGTGCTTTAACACTA	143279
rs542642702	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91411704	CAATGCAGCAAATTG[C/T]GAACAGTAATGATAC	143279
rs542667853	snp	C/G	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491696	ACATCTATAAAATTA[C/G]AGGTCTGACCTACAG	143279
rs542671189	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91479000	GAGAAGGCAGAGAAG[C/T]ATAAAGAAGAAAGTG	143279
rs542733121	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449559	GGCAATCAGGCAAGT[G/T]AGAGAAATAAAGGAC	143279
rs542756266	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449149	TACTGGCAAACCAAA[C/T]GTAGCAGCGCATCAA	143279
rs542760603	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91473492	GATCTGAGATATAAG[A/C]AAGAATGATGAAAAA	143279
rs542799926	snp	A/C			upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409152	TAAAAAATCTGATAG[A/C]GCTGAATATCGAAAT	143279
rs542851077	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91510821	ATTAAGAATGTTAAA[C/T]CTTACATATGAACAA	143279
rs542857987	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482390	AAGTATTCCTTCAGC[A/G]TCCCTTTATCATTTA	143279
rs542923993	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431058	CTTCCTTCAGGAGCT[C/G]TTTTAGGGCAGGCCT	143279
rs542950402	in-del	-/AGTC	0.0023933	0.0345097	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91474620	AAGAGTTGAGCAGTT[-/AGTC]AGTGAGTATGTATTG	143279
rs542964721	snp	C/T	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476386	GATCACCACACCTGC[C/T]CAATCACCCAGAAAT	143279
rs542970046	snp	C/G	0.00318978	0.0398085	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433653	CCACAATGAATGACT[C/G]TGTACATATGTCGCT	143279
rs543029646	snp	A/G	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420756	TAGTCAGTCTTTTCT[A/G]TATTCCCCTGTCTAA	143279
rs543082429	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419836	TTTGTAGGCTGGCCA[C/G]ATTCCAGGCCATCAT	143279
rs543091387	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91510375	TCAGGCTTAAAAGAT[A/G]TACATAATTTGGTCC	143279
rs543091763	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412838	GATTGACTTTTACAG[C/G]AGCTAGGAAGGCCTT	143279
rs543094811	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419386	GGTTGAAAATATTTA[A/G]CTATATGTTAATAGC	143279
rs543122217	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91436897	TATTTCACCTGTTCT[C/G]TTTGTCCTTATAGAC	143279
rs543157194	snp	C/G	0.0166325	0.0896639	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91428039	TCTTTAATCCATCTC[C/G]AATTAATTTTTGTAT	143279
rs543267078	in-del	-/AGCGGCGGCTAGA	0.0267878	0.112589	utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410319	CGGAGTGGCGGCGGC[-/AGCGGCGGCTAGA]AGCGGCGGCTAGAAG	143279
rs543285578	snp	A/G	0.00199481	0.0315187	intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91463382	GAAGAGGAGGGGTTG[A/G]TCTTGCTGTCTCAGG	143279
rs543324722	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91455122	ATGGTATTTCTAGTT[C/G]GAGATCCTTGAGGAA	143279
rs543325157	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409050	ATTTGGGTTTGTTTC[A/G]GAGATATTTTTGGTT	143279
rs543328266	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91474975	AAGGCCCTGAGAAGG[A/G]AACACAATTGGCAAA	143279
rs543331551	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432583	TCCTTTCTAAAGTTA[A/T]GATGCCCCTTTCACA	143279
rs543359289	snp	A/G	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467505	CAGGGCCTCAGCCTC[A/G]CCACACTCACTTGCA	143279
rs543380867	snp	A/G	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450286	GGGAAAGGATTCCCT[A/G]TTTAATAAATGGTGC	143279
rs543385536	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462294	CTTAGAAACTCTGAT[A/G]CAATTTTATAGTAAA	143279
rs543390278	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91408258	TCTGGTGCAGTAGCA[A/G]AAATTAACATTTTTG	143279
rs543390508	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467886	AGCAACTAGCCCCCC[C/T]ACCATGCTGACACCA	143279
rs543394976	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91466222	CATAGAGTTGTTCAT[A/G]ATAGTCATAAATTAT	143279
rs543428454	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91417305	CATCAAAAAACATTT[G/T]TTGAAATAATGAAAT	143279
rs543487112	snp	A/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457351	CAGAGAAAGATAGTT[A/T]AAAAAAAATAAAAGA	143279
rs543490953	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91416541	ATATCATATAACCTA[C/G]GTGTGTAGTAAGCTG	143279
rs543496824	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91424661	GTTATTTTGTGAAAG[A/T]TGTGATAATGGATAG	143279
rs543529026	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91466675	ATGTATTTACCCAAA[A/T]GAGTTAACAATTTAT	143279
rs543552798	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476697	CTGGCTTCTTTCTCC[A/G]TCCCTGTGTCAAGCT	143279
rs543558190	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91423753	TTTGGGCTCTTTTAT[A/T]TTAATTTCTTTAAAA	143279
rs543567450	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91435653	TGTCTCTGTCTCTCT[C/T]GAAGCTTGTTGAGCC	143279
rs543594398	snp	A/G	0.0023933	0.0345097	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439420	CTGAGACCTTTATCC[A/G]GTTCCATTGGTCTAT	143279
rs543641000	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91495710	GAAATTACCTATCCT[A/G]TTAGCTTATCAATAG	143279
rs543681915	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440283	GAGAGTTTTTAGCAT[A/G]AATGGGGTGTTGAAT	143279
rs543733215	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509189	AGATGACGGGTTAGT[A/G]GGTGCAGCACACCAG	143279
rs543769529	snp	C/T	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91454815	GTGAGTGAGAACATG[C/T]GGTGTTTGGTTTTTT	143279
rs543816192	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449844	AGGACCTCTTCAAGG[A/G]GAACTACAAATCACT	143279
rs543817143	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91514120	GTAGGTTACCACTTA[C/T]AAGCACAAAAGAAAC	143279
rs543851302	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91513092	CAGACTAATTGGATT[C/G]AAGGTTATATTCTTT	143279
rs543964425	snp	A/G	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91479116	CTTACTCAGGAGGCT[A/G]AGGCAGGAGAGTCGT	143279
rs544015197	snp	C/G	5.06872e-05	0.00503399	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461373	TAATTATACATAAAA[C/G]ACACTTTTCATTTCA	143279
rs544021717	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432345	ACTGCAAAAACCCAG[A/C]GTGGGTTCACCTAAC	143279
rs544055820	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503469	GCCTCACTCGGGAAG[C/T]GCAAGGGGTCAGGGA	143279
rs544082607	snp	A/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439727	GAGGATGGAATGTTT[A/T]TCCCTTTGTTTGTGT	143279
rs544105424	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445883	TTTCCATGGTCTTTA[C/T]AACCTACAGACAAGG	143279
rs544108612	snp	G/T	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91429260	AGAAGCTTTTTGATG[G/T]GCTGCTGGATTCGGT	143279
rs544111946	in-del	-/AA	0.0115144	0.0749975	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452723	CAGATGCAGCACCTC[-/AA]AAAAAAAAAGGCATT	143279
rs544169604	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91436984	AGGAATTAAAATATG[C/T]TCAGTCTGACATCTT	143279
rs544182069	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485560	TCTATCTTAATATGC[A/C]GTCTCTTATCTCTTA	143279
rs544199543	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501039	TCAAAAGTCTAATAC[A/G]TATATAGAAGCTCAC	143279
rs544240466	snp	C/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91507075	GACAAAATTCAACAA[C/G]GCTTCATGCTAAAAA	143279
rs544271800	snp	A/C	4.97187e-05	0.00498567	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462064	GTCTTTAAAATGTTG[A/C]ATATACTTAATTCTT	143279
rs544409960	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91465887	GAGAGGTATTGATCT[A/G]TACTTTTCCTTTCTT	143279
rs544418583	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91505029	GCCAAACTAAGCTTC[A/C]TAAGTGAAGAAGAAA	143279
rs544431090	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91469658	CAAAAACACACTTAA[A/G]CACATAAACTATTGA	143279
rs544444658	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419169	TTGGAGTATAGAGGA[C/T]GATCAAAGTAAATTT	143279
rs544447609	in-del	-/AA			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420224	AATTATTTTACAAAC[-/AA]GAGACTTATTAGACC	143279
rs544581223	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487328	GAGCACCTGGGTTTT[C/T]TGTACTACTTAACCA	143279
rs544596429	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426806	TCCTTCTCATCTGTG[C/T]CAGTCTTGTGGAATC	143279
rs544629568	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477136	CAGTGAGCCGAGATT[A/G]CGCCACTGCAGTACG	143279
rs544660328	snp	C/T	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439441	ATTGGTCTATATATA[C/T]ATATCTGTTTTGGTA	143279
rs544683262	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433791	CCAGGACCTAGCATT[C/T]GTGGTGCATGTAGTC	143279
rs544710188	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444167	ACACACTTTTTCCCA[A/G]CCTGGCTATAAACAC	143279
rs544722619	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91443587	GAGGAGGCAGTCTGT[C/T]CCTTAGCAGAGCTTG	143279
rs544730065	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497347	CCAGGCTAGAATGCA[A/G]TGGAACAATCTCAGC	143279
rs544735782	snp	C/G	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431165	GCTGGATATGAAATT[C/G]TGGGTTGAAAATTCT	143279
rs544787039	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91407284	CAGGCTGGTTTCAAA[C/T]TCCTGACCTCAAGTG	143279
rs544832339	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477726	TGAAGTTTCTTGTTA[A/T]TGAAGCTTCTATTCT	143279
rs544847820	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415394	GATATTACAAATATA[C/G]AAAATAAGTGTTTAT	143279
rs544876481	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91469007	GACCAAGCTAAAGAA[A/G]GAATTTCAGAGCTCA	143279
rs544932153	in-del	-/ATTA	0.00358779	0.0422022	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451947	TAAAATCTATAAGAT[-/ATTA]ATCATTCTGTTGTTT	143279
rs544945861	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91488362	GAGCAGTATGAAGTT[A/C]TCTCTCAGTCTGTCC	143279
rs544975850	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471911	TACAGTTGCAGTGCT[A/G]TTGCAATCAAACTAC	143279
rs544991749	snp	A/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493350	AGATGAGATGTCATG[A/T]ACATGTTTACCACTT	143279
rs545045518	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91463505	TTAATTCTAATAGTA[C/T]ATCAGTAAATTAACT	143279
rs545086487	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471449	ACTCCTGTTCAACAT[A/G]GTACTGGGAGTCTTA	143279
rs545116461	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439180	GAATGGTATTGCCTA[C/G]GTTTTCTTCTAGGGT	143279
rs545144776	snp	A/G			intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481920	AAGAACATATACAGG[A/G]TAGGGATAGAGAAAG	143279
rs545145067	snp	C/T	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438339	CATGCAGTGTTTGGT[C/T]TTCTATTCCTATGTT	143279
rs545160850	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91413236	GAGTTAGGCTGTATC[C/T]TTTATGTTTACAGAA	143279
rs545173093	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512867	GCAAATGCAGTTTAC[A/G]GGGATTTTTGATATA	143279
rs545175366	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502135	TTAGATCATATTTCC[A/G]TGGGAAATAACTTTA	143279
rs545198223	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91466758	CAAAAATGTCCTTCC[A/G]TAGGTGAAGGGATAA	143279
rs545235590	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451319	AAGTGGGAGTTGAAC[A/G]ATGAGAACACAGGTA	143279
rs545288928	in-del	-/G	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91454135	ACTAGCTAGAAAATC[-/G]AACAAGTATGTAGAA	143279
rs545307227	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422890	GTGAACTAAGCAATA[A/T]TCTTTGAGACTTCTT	143279
rs545308431	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91474371	AAATTATATTCCATG[C/G]TAAGCACAAGAGATA	143279
rs545310476	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91465912	TTTCTTGTAATATCT[G/T]TCTCTTTTGAGCATT	143279
rs545370158	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91473513	TGATGAAAAAGAAAT[C/T]CATAAATACAGTTGA	143279
rs545387893	snp	C/T	0.00517822	0.0506191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91456053	ATTGACTTAGCAATG[C/T]GGGCTGTTTTTTGGT	143279
rs545464451	snp	A/G	0.00279162	0.0372561	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412633	TTATTTATTTTTTAA[A/G]AAAAAAAACAATTTA	143279
rs545476910	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467987	CCACCACTGCTGCCA[A/G]CTCAAGAGCATGGAG	143279
rs545499727	snp	A/G	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91430338	TGTGGTGTGGTGCTG[A/G]AAAAAATGTCTATTC	143279
rs545518389	in-del	-/C	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421033	AACCTTTGCATTCTT[-/C]CCCCCCCTCAGGCTT	143279
rs545536020	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420223	CAATTATTTTACAAA[C/T]AAGAGACTTATTAGA	143279
rs545549088	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91417519	AATGCTATCCCTCCC[C/T]GCCCCCCCACAACAG	143279
rs545572282	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91506375	AATTGATAGACCGCT[A/G]GCAAGACTAATAAAG	143279
rs545610802	snp	C/T	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91505303	TAAATGGACTAAATG[C/T]TCCAATTAAAAGACA	143279
rs545622752	in-del	-/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91494960	TGAAATTGCTCATTG[-/T]TTTTTTTTGCAATAG	143279
rs545650578	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449680	TTAAGCTGATAAGCA[A/G]CTTCAGCAAAGTCTC	143279
rs545681334	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91456775	AAGTTTCAAAACAAA[C/T]ATCTAAGCCTTTAGC	143279
rs545753256	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91459651	CTAATAATGTACTTT[C/T]CTGTTTCCAGAAATA	143279
rs545779013	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91424156	GTTGCCACAGTCGAG[A/G]AAAAGAGAGAAGAGC	143279
rs545819478	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409131	ATAAAATAATGAAGG[C/T]ACAGATAAAAAATCT	143279
rs545876097	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439044	CTCTTCACTCTGATG[A/G]TAGTTTCTTTTGCTG	143279
rs545891264	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421086	TGAGTCATCCTTGCT[C/T]ATTGCTTTCATTTTC	143279
rs545922723	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91456204	GATTCTTCCTATCCA[C/T]GAGCATGGAATGTTC	143279
rs545978661	snp	C/T	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458494	TGTTTTTTAAAAGAA[C/T]AAAGTTGAAAGAATC	143279
rs545990593	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91507380	TCTAGAAAACCCCAT[C/T]GTCTCAGCCCAAAAT	143279
rs546024358	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449822	ATACAACTTACAAAG[G/T]ATGTGAAGGACCTCT	143279
rs546045214	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432901	TCAGCTGAAATCGCA[A/G]TTGGATCTGTGTGTG	143279
rs546046109	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91486221	GAATGGGCTTCTGGA[C/T]ACATCTCATTTCACA	143279
rs546085259	snp	G/T	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496819	CTAATCATGCTATTA[G/T]TTACCTTTTTCTAAT	143279
rs546085593	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452427	AATGCTGCAGTTTGA[A/G]TATTTATTTCCACCA	143279
rs546134552	snp	A/C			intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462531	TATCAGAATCACAAG[A/C]AGGGCTTGTTAAAAT	143279
rs546213233	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497196	GGCCAGGCTGGTCTC[C/G]AACTCATGGCCTCAA	143279
rs546224673	snp	C/T	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91428541	ATTTGTTTATATCCT[C/T]TTTTATTTCATTGAG	143279
rs546233241	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501424	TCAGGATGTGTACTC[C/T]GTTTGAAGTTATTTT	143279
rs546237666	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503519	GAAAGGGGTGACGGA[C/T]AGCACCTGGAAAATC	143279
rs546270886	snp	G/T	0.000265138	0.0115108	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478193	TTACTGTTTTCTTTT[G/T]CCTACAGCCTCAAGA	143279
rs546274056	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91514611	TATCAGTATTTTTTA[A/C]ACATCCTGTCCTTTT	143279
rs546285066	snp	A/G	0.00993419	0.0697739	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451441	AGGTTGATGGGTGCC[A/G]GAAACCACCATGGCA	143279
rs546289668	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457962	AGAAGAAAAAAGACA[C/T]ACAGATTAGAAAATA	143279
rs546289916	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91436382	TAATCAGATTCCCCA[C/T]GAAAGTGTCTTCCAG	143279
rs546298532	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91435620	CCTGTTCCTTTGAAT[C/T]AGATGTCTCTCTACC	143279
rs546299132	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91489289	ATCAGTTTTTTATGG[A/G]TGTTTCCCAACATTT	143279
rs546343421	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462534	CAGAATCACAAGAAG[C/G]GCTTGTTAAAATACA	143279
rs546358977	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91416591	AGTACACTCTGTGAT[A/G]TTTGCACAGCTACAA	143279
rs546383386	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485588	TTACTATTCTATGCA[C/T]AGGGGTCAGCAAAAC	143279
rs546415647	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410890	TGCATCTTGAGTCGG[C/T]ATGATCTGTTGGATG	143279
rs546510602	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91427813	TGCGAAAAATTTTTC[C/G]CATTTTGTAGGTTGC	143279
rs546512734	snp	A/G	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91429319	ATCAATGTTCATCAA[A/G]GATATTGGTCTAAAA	143279
rs546516644	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91495822	GCTATCTCCAAAATC[A/C]GTATTCTACAGTGAG	143279
rs546521111	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470186	AACAAAGATACATGG[C/G]ACCTGAACTTGTCAT	143279
rs546530211	snp	A/C	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91411143	TACAGACATGTGACT[A/C]AGGTGGGGGGAGGCT	143279
rs546557522	snp	A/G	0.0023933	0.0345097	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490342	TATAGATAATGCTGT[A/G]ATAAACATTGTACTG	143279
rs546568044	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409988	CCCTTTGCAGGGCTC[C/G]ACTTGTCTCCCCGAC	143279
rs546601731	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419518	TGAAGCCCACATTAG[G/T]TACTTGTGAAATAAG	143279
rs546696812	in-del	-/GG	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91436158	TTGTCTGTTTGTTTT[-/GG]GGTCTCTGTCCTCCA	143279
rs546802013	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426258	TTATCACGGGAAATG[C/T]ACATTACTTAAATAC	143279
rs546810427	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476696	GCTGGCTTCTTTCTC[C/T]GTCCCTGTGTCAAGC	143279
rs546813802	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412159	TCCTAGCCAGTTCTC[C/T]CTAATCAACCATCTT	143279
rs546815405	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444945	TCTTTTAATATACTG[C/T]TGCCAATTTTAGCTG	143279
rs546815433	snp	A/G			intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482217	TGAGTTGTTCTGTCA[A/G]TAAGTCAGTTTTGAA	143279
rs546827469	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478305	GCTAATCAGTATAGA[C/T]GTCTAACTTACACAT	143279
rs546851412	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444642	AATATCAAGGCATTG[C/T]TTCCAGAGACAGGCT	143279
rs546903740	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91479317	ATTTTAATGTATGTC[C/T]TTTTAGTTTCTATCT	143279
rs546961557	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91453695	AGACTTAAGTTCTAC[C/T]TTATTAAAAATTACA	143279
rs547036746	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468346	GCCATTCAGCTGAAC[C/T]CACTTTATACCACAA	143279
rs547057039	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439446	TCTATATATATATAT[A/C]TGTTTTGGTACCAGT	143279
rs547116901	snp	C/T	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91414821	CATGCTGGGAACTTG[C/T]GGGAGGTGAGAAAGA	143279
rs547209915	snp	C/T	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91507493	ATAACAGACAAACAG[C/T]CAAATCATGAGTGAA	143279
rs547212017	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498818	ACAAACCTGTTCACC[A/G]AAGTATGTTATTATA	143279
rs547212450	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426437	TAAATTATTCTTGCA[C/T]AGAGATTTTCTGTTT	143279
rs547246828	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91505998	TCAACTACATGGAAA[C/G]TGAACAACCTGCTCC	143279
rs547268632	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422381	AGCTAAGTTAACAAA[A/G]GTCTGTTGCTGAGGG	143279
rs547272278	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503583	ACGGGCTTAAAAAAC[A/G]GTGCACCACGAGATT	143279
rs547305222	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433422	CTTTGGTGGGTAACT[A/G]TGTATGCATTGTCCA	143279
rs547372378	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457041	AATAATAAGGGAATA[C/G]TGCAAACTCTACACA	143279
rs547383118	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501423	ATCAGGATGTGTACT[C/G]CGTTTGAAGTTATTT	143279
rs547433441	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91465055	TAAAAAAACACATGC[A/C]AAGACTATAAACAAA	143279
rs547533887	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439444	GGTCTATATATATAT[A/G]TCTGTTTTGGTACCA	143279
rs547552071	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91447682	ATGGAGGAATATTTC[C/T]CACACAAATGGAAAG	143279
rs547676680	snp	A/G	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91480788	TATTAAAACAAAAAC[A/G]TAAGTATTCTAAAAT	143279
rs547712675	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421537	TTATAATGTTTTAAG[A/G]AAGTTTATGAATTTG	143279
rs547742752	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449310	CACTTAATTACCTCA[A/G]TAGATGTATAAAAGG	143279
rs547756054	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457680	AGCATCTAGAAAAAA[C/T]CTGCAATTAACATTT	143279
rs547782312	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497627	CAGAAAATGTTTCTT[C/T]CAGTATACTTAACTT	143279
rs547861102	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452490	CAGTGTTGAGAGGTC[A/G]GACCTTTAAGAGGTA	143279
rs547962931	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481715	AAGCAATTTTTACTT[C/T]TTATTATTTTTTGAG	143279
rs547964192	snp	C/G	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431668	TTCTTCCAGTTGATC[C/G]CATCGGCTCCTGAGG	143279
rs548041956	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91486718	ATCTTACTGAGTTCA[C/T]TGCATTTTCTTTTTA	143279
rs548046682	snp	A/G	0.0221141	0.102801	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431190	AATTCTTTTCTTTAA[A/G]AATGTTGAATATTGG	143279
rs548106948	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438557	GTGTGTGTGTCTTGA[C/T]AGTAGAATGATTTAT	143279
rs548108713	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91430653	CTTCTTTGTCTCTTT[C/T]GATCTTTTTTGGTTT	143279
rs548120934	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437963	CTTTTTTTAAAAAAA[A/C]AATTTATTAGAGCAT	143279
rs548202841	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91424149	CTGGATGGTTGCCAC[A/G]GTCGAGGAAAAGAGA	143279
rs548240707	snp	C/T	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91504003	AACTGGGAGGCACCC[C/T]CCAGCAGGGGCACAC	143279
rs548244486	snp	A/G	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440782	TCTATTCAGAGATTC[A/G]ACTTCTTCCTGGTTT	143279
rs548265572	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432636	AGCACAGAATATCTT[A/T]AAAAGAAATGAAGCA	143279
rs548281985	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502612	AAAATAAATATTTAC[A/G]TATATAATTAAATTT	143279
rs548312988	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431519	CTTTCAGGTACACCA[A/G]TCAGACGCAGATTTG	143279
rs548394570	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440087	CTTTCTCTTGCCTGA[C/T]TGCCCTGGCCAAAAT	143279
rs548400249	snp	A/C	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91417963	TCCACAATGGTTGAA[A/C]TAGTTTACAGTCCCA	143279
rs548413986	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478656	CTATTATAGGGACGC[C/G]TAAGGCCAGCTACTA	143279
rs548430214	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91427264	ATTGTTGGACATTTG[A/G]GTTGGTTCCAAGTCT	143279
rs548445760	snp	C/G	0.0111196	0.0737302	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91411036	CAGATTAAACAGGCT[C/G]TGCGGCGAGTTTCCA	143279
rs548455310	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91435460	GGAATAAGAAGTAGG[C/T]TCATCTGTACATTCT	143279
rs548493938	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426417	TCCATAAGCTGCATG[G/T]GGTATAAATTATTCT	143279
rs548495323	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91453693	ACAGACTTAAGTTCT[A/G]CCTTATTAAAAATTA	143279
rs548497631	snp	C/T	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467189	AGCCTGCTCTTGCCA[C/T]GGGCCTCCGGAATCC	143279
rs548509962	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450348	TGAAACTGGACCCCT[C/T]CCTTACACCTCATAC	143279
rs548515030	snp	A/G	0.00993419	0.0697739	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467569	GGGGCATAGCTCACC[A/G]GCAGACCACTCCTGA	143279
rs548537661	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91408680	CCTGAAAAAGAATTT[A/G]GAAAAATATTAATAG	143279
rs548549754	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91416791	AGCCTCAGGCCCTGT[A/G]TGTATTGCCTTTGCC	143279
rs548565734	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484400	AAATAGAATTTGGGG[A/G]AATAGTCTAAAATTT	143279
rs548579726	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468489	CCAGAACAAGAACTC[C/T]GGCAACTCAAAAAGC	143279
rs548596403	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91430514	AATGTGTGGGAGTCT[A/G]AGTCTCTTTGTAGGT	143279
rs548627513	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91495035	ATGTTTAGATATTCT[A/G]TATTTCAAGTTAAAC	143279
rs548658870	snp	A/C	0.0023933	0.0345097	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91429393	TGATGCTGGCCTCAT[A/C]AAATGAGTTAGGGAG	143279
rs548673235	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91428786	TTTTGGGCTGAGACA[A/G]TAGGGTTTTCTAGAT	143279
rs548698644	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426778	CTTATTTGAGCTTCC[A/G]TCAATGTGTGCTTCC	143279
rs548720494	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91456253	TGTTTTATTTCGTTG[A/T]GCAGTGGTTTGTAGT	143279
rs548731337	in-del	-/T			intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462816	ACTGCTATAGATCAA[-/T]TTGTGAAAAATTGAC	143279
rs548753096	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483297	ATTTGTTTGCACAAG[C/T]TGTTGAGAATTTCTG	143279
rs548800940	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460646	ATCTTTATTTGAGAA[A/T]TTAACTTTTGGATCA	143279
rs548840025	in-del	-/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498308	ATACAATCCTCTGTC[-/T]TTAAAGGACCTTAAC	143279
rs548855346	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464889	AAAAAATTAAATATA[C/T]AGATATGAGGGAAAA	143279
rs548880332	snp	G/T	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421069	CCCTTCAGTAAAGCT[G/T]CTGAGTCATCCTTGC	143279
rs548999104	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91479460	TCATACTGTATAGTT[C/T]CATGTGACTTTTAAC	143279
rs549029210	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412250	TTTCAGATTAGGTGC[A/G]TGTTTTTGCCACCAA	143279
rs549034985	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462728	ATGATAAAGACAGAA[G/T]GTAAACAAAGTCTCC	143279
rs549063933	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437088	TTATACATGTTCCAG[C/T]ATCTATTGAATATAT	143279
rs549169834	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410137	GGCCCTCGGGGTTGA[C/T]GAGGGGGACTACCGC	143279
rs549176093	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91463997	TTTGAATTTAAGTCG[A/T]TTTTTGCAAACTAAG	143279
rs549189418	snp	A/C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439521	TCAGGTAGTGTGATG[A/C/T]CTCCAGCTTTGTTCT	143279
rs549284539	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471556	TATTATTCTATACCT[A/C]GAAAACCCCAAACCC	143279
rs549303847	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437944	TTTTGATTGTGACAA[A/G]ACACTTTTTTTAAAA	143279
rs549348633	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91453767	ACCAAAAACATGACC[C/G]AACTGTTTTCTATTT	143279
rs549356969	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503737	GCTTGCTTAGGTAAA[C/T]GAAGCAGCCAGGAAG	143279
rs549375228	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502344	ATGTGCCAGCTATGA[C/T]TATTAAAGACACAGT	143279
rs549392542	snp	C/T	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445566	TCAGTTTAGACATTA[C/T]ACAATGAAAGAAGAG	143279
rs549407372	snp	A/G	0.00517822	0.0506191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410979	GCCTTGGAGGCGCGC[A/G]GATTTTTGTCCTTTT	143279
rs549491466	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91474933	ATCTGTGAGAGCAGC[A/G]CACTAACAGAAGTGA	143279
rs549512974	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91418810	GTTTATTAAAAATTG[A/G]TAAAGTAGGGTATCT	143279
rs549517756	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445973	CCATTTGAGCAGACA[C/T]CGAACTTGCTGCAGG	143279
rs549524936	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91466964	TAGATGCAGCCAGGA[A/G]GAACATCTGCCACGG	143279
rs549552540	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500377	GTCGATTTTTCTTCA[A/G]CAAAAATGGTTTGAT	143279
rs549559433	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91407547	TTCTAAAATTAAGGT[A/T]TTAGTGGTATAAACC	143279
rs549630788	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484806	TTTCTACTTTGATAA[C/T]AGATTTCATAATTTA	143279
rs549667542	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492169	TCTGTTTCCTGATCT[A/G]TAAGACATAGTAAAC	143279
rs549843442	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449843	AAGGACCTCTTCAAG[G/T]AGAACTACAAATCAC	143279
rs549895877	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91466251	ATCCTTTTAATGTCT[A/G]TAGAATCAGTGTGAG	143279
rs549900866	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91456912	AAAGAGATGGCTCTT[C/T]GACAAGATCAGTAAA	143279
rs549904811	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449421	GAACTATTTATGACA[A/G]ACCCACAGTCAATAT	143279
rs549997514	in-del	-/T	0.0715223	0.175059	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497288	GCCAGAAAATGTTTC[-/T]TTTTTTTTTTTTTTT	143279
rs550029404	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440120	CCAATAATATGTTGA[A/C]TAAGAGTAGTGAGAG	143279
rs550058045	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91416818	TGCCTTTATAAACCT[C/T]CACCGTCCCCCTCAC	143279
rs550098418	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481966	AAGTGGAAAAGGGGG[A/G]AAAATGACCAAGAGG	143279
rs550117585	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438765	ACTTTTTACTGATCG[C/T]CATTCTAACTGGCAT	143279
rs550124644	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433483	CTAGATATCTTTCTG[C/T]ATCAGTACATAGAAA	143279
rs550198333	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431737	CAGCTCCATCAGCTC[C/T]TTTAGGCACTTCTGT	143279
rs550212429	snp	C/T	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439285	ATTCCAGTTTCAGTT[C/T]TCTGCATATGGCTAG	143279
rs550235300	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468246	ACAAAGCCAGGGGCT[C/T]GGTACCAGCACCCCC	143279
rs550257987	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444487	TGCAGAATGTTAACA[C/T]ACTATGTTAATGGAA	143279
rs550270460	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91453468	ACAGGGGATGGTAAG[A/G]GAGGTAGGATTTCTG	143279
rs550302641	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437278	AGGCTTGATCATTCC[C/T]ATGCCTGATGATTGA	143279
rs550310697	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91473750	ATAACATTATCTTTT[C/T]TCTATTTTATAAGAA	143279
rs550321384	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470004	GGTATAGAGTTCAGT[C/T]CAACAAGAAGACTTA	143279
rs550322296	snp	G/T	0.00398564	0.0444627	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498757	TTAGCCTTTTATAGT[G/T]TATGTGTTTAGAAGG	143279
rs550338687	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91435595	GCTGCCACCTCAGGC[C/T]GCTGTGATTCCTGTT	143279
rs550437114	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439943	ATTTTGTATCCTGAG[A/T]CTTTGCTGAAGTTGC	143279
rs550445170	snp	A/T	0.00874735	0.0655527	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476067	CATAGAGCAAAGTGG[A/T]GAAGAACAGCAAATC	143279
rs550488325	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422231	TCATATCTTGCTGGA[C/T]CATTCTCCCTTTCTG	143279
rs550593772	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91416880	CACTCCCCAGAATTA[A/C]GGGATGTCATGCACT	143279
rs550627588	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91454153	CAAGTATGTAGAATA[C/T]AGAATACCTCAGTGC	143279
rs550650551	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91505921	ACACTATAACAAACT[A/C]TCTCTCAGACCACAG	143279
rs550729512	in-del	-/T	0.00202634	0.0317658	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477473	CTCAGGGGCAAACAC[-/T]TAAGTGGTTGAGCAG	143279
rs550734863	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452796	AGGATATGCCACTAA[A/G]TTTTTCAAATGCTAA	143279
rs550789482	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425180	ATCTATTATCTACTC[A/G]TCATCAAATTAAAAT	143279
rs550820829	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409274	GGAAAAGGAGGGGGC[A/G]ACAAGAAAGGAAAGG	143279
rs550849966	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91418857	TAACTTGAAACCTAT[A/T]AATATATGTTTATTT	143279
rs550856473	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91436252	CCAAGATGGATGATT[A/G]GAAGGTGAGGCATAA	143279
rs550883825	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91417612	CGAGTGAGAACATGC[A/G]GTGTTTGGTTTTTTG	143279
rs550892965	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91489157	TATCTTTTTGTGGAA[G/T]TTTTCTTCTACTTTA	143279
rs550900018	snp	C/T			upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91408972	TCTCATGATGCACCA[C/T]AACTAGTATTTAGTT	143279
rs550911665	snp	C/T	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467665	TCAGAACCTCCCCTC[C/T]GTAGCTTTGCCAGCA	143279
rs550912672	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439708	ATTGATTCTTCCTAT[C/T]CATGAGGATGGAATG	143279
rs550940700	in-del	-/TTTA	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461142	ACTGGGACATATTTC[-/TTTA]TTTGGCTTCAGTATT	143279
rs550955961	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476606	ACCACCGCAGGCATC[C/T]GGGGAGGAGTGCCAA	143279
rs550977305	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91459944	AGTAGGCTATACCAT[C/T]TAGGTTTGTGTAAGT	143279
rs550981329	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426112	TAGAATATGAATCCA[A/G]CGTTTTTAAGTGCAG	143279
rs551047113	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464371	GAAAGCAAGTAAAAA[A/T]TATTGCAGATGGACC	143279
rs551134056	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485806	TGCATGATCTAATAT[A/G]TTGATCACACACAGA	143279
rs551135585	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449943	ATATCATGAAAATGG[A/G]CCATACTGCCCAAAG	143279
rs551189495	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91504908	CTCAAAGAGAAGCCC[A/G]TCAGACTAACAGCGG	143279
rs551280092	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91510631	GGAAATGTTATTGAA[G/T]GGATGCATGAAACAC	143279
rs551355061	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91472602	AAAAAACTGAAATAA[C/T]AAGCAAAAGCAAACG	143279
rs551413495	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421255	TATTTAACATTATTG[A/G]CCTTTTTTTTTTCTT	143279
rs551418370	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471633	CTGAATGCAAAATCA[A/G]TATATAAAAATCAGT	143279
rs551441123	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471426	AGACAAGGATGCCCA[C/T]TCTTAGCACTCCTGT	143279
rs551472776	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91430552	GACTTGTTTTATGAA[A/T]CTGGGTGCTCCTGTG	143279
rs551506529	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470823	AAAAGCCCAGAACCA[A/G]GTGGATTCACGGCCG	143279
rs551534546	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91480523	CCAAATAGATCTTGA[A/G]CAGGCAAGAAACACT	143279
rs551593427	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91513199	TTTCTTCTTAAGGCT[C/T]AAGATATTAGAAAAG	143279
rs551695882	in-del	-/TA	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91443863	TTTTATATCCTTTAT[-/TA]TAAATATGGCAACAT	143279
rs551700910	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490747	ATACAAAAAATTAGC[C/T]GGGCGTGGTGGTGGG	143279
rs551721890	snp	A/G	0.0115144	0.0749975	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91429566	TCAGATCCTGTTATT[A/G]GCCTATTCAGAGATT	143279
rs551744329	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500447	GAAAATAGTTCCAGT[G/T]TCACTTAAAACCATC	143279
rs551827150	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91515081	AGATAGATAACTTCA[C/G]CTCTTAAGTAAGTAT	143279
rs551839980	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462475	AATTATATTGGAATT[A/G]CACTGAATCTGTAGA	143279
rs551855678	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91411929	GTTTAAAACAGTAAA[C/T]GTATGTACTTATAGA	143279
rs551862403	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451516	CCAGAACTTAAAGTA[C/T]AATAATAAAAAAAAA	143279
rs551898146	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467540	ACCCTCGATGCCCAA[C/T]CAAGGTACTTCCTGG	143279
rs551967410	snp	A/C	1.67595e-05	0.00289473	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501332	TGAAACTTCTACTAA[A/C]TGGTAAATTTCTGGA	143279
rs551973729	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497391	CACCTCCCAGGTCCG[A/G]GCAATTCTCCTGCCT	143279
rs552010853	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496444	CTGCACAGTCTCTCC[C/T]CCTAATGCTATTCTT	143279
rs552010938	snp	A/G	0.0391387	0.134304	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91504596	AGAATAAAAAGAAAC[A/G]AGCAAAGCCTCCAAG	143279
rs552042244	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452731	AGCACCTCAAAAAAA[A/G]AGGCATTGAAATAAC	143279
rs552068808	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91486698	ACATAGTAAAACTAA[C/T]ATATATCTTACTGAG	143279
rs552097146	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437177	ACAAATATGTAATTT[A/G]TGTGGAGATCAGTGG	143279
rs552099018	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449202	GAACTTACCCACCAC[A/G]ATCAAGTTGGCTTCA	143279
rs552105763	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91486631	ATCATTCACAAAGTA[C/T]CATTTCTCTTGTGCA	143279
rs552109649	snp	C/T	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91446137	GAGCTCCAGCTGGCA[C/T]CTGGCAGGTGCCCCT	143279
rs552230633	snp	A/G	0.00279162	0.0372561	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91511404	TTAATACTAAAAACC[A/G]GAATAATAGTATCAT	143279
rs552235638	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451075	ACACATGCACACATA[C/T]GTTTATGACAGCACT	143279
rs552244816	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426601	GCACACACACACCCC[C/T]CCGTCACGCCAATAT	143279
rs552259810	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450318	GGGGAAACTGGCTAG[C/T]CATATGCAGAAAACT	143279
rs552269298	snp	A/G	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91495108	GTGTTTATCACACAC[A/G]CAGATATAAAACCTA	143279
rs552270766	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91408498	TATCAACCTAGACTT[A/G]GCACAGAATATCTGA	143279
rs552372278	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91475039	TGAATTTGGGAGAAA[A/G]GAGAAGACTAGGTTG	143279
rs552438302	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433902	GAATGTCAAACCCAT[C/T]TCAAGGCTGTAATAA	143279
rs552475313	snp	A/G			intron-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483228	CAGTTACAAAAATCT[A/G]CTTTAGTACTACATA	143279
rs552482964	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91473926	GCATTCCTAACTCTC[A/T]TGTTGTTCAAGGGTC	143279
rs552500118	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91443656	TGGCAGGCAGGAATG[C/G]TTAAGTCTGCTGAAG	143279
rs552512527	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440670	ACAGCTCCTCTTTGT[A/G]TCTCTGGTAGAATTC	143279
rs552537961	snp	C/T	1.67697e-05	0.00289561	synonymous-codon, intron-variant, nc-transcript-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483053	GGAAGCTGACCATCA[C/T]TTCCTAGTTCACTGG	143279
rs552553836	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91423936	GTTTTATAGAAATGG[C/T]GAACACTGGAAAAAG	143279
rs552554241	snp	A/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468776	TCTCTACAAAAAAAA[A/T]TTTTTTTAAGTTAGC	143279
rs552608730	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91434807	TAACATACAAACTGT[A/G]CAATCCTAGAAAATT	143279
rs552650831	snp	C/T	0.0898077	0.191933	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91427717	TTTTTCTTGTAAATT[C/T]GTTTGAGTTCATTGT	143279
rs552730037	snp	C/T			missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492356	TCTTCAAATAGCTAA[C/T]CCGGAAAAGAGCCGA	143279
rs552731646	snp	C/G	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496434	TTTTTTCTACCTGCA[C/G]AGTCTCTCCTCCTAA	143279
rs552795737	snp	G/T	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91506679	GATGGATTCACAGCC[G/T]AGTTCTACCAGAGGT	143279
rs552806618	snp	A/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91473494	TCTGAGATATAAGAA[A/T]GAATGATGAAAAAGA	143279
rs552843641	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445112	TTTTGCTAGCTCACT[C/G]TTTTCACAGACGTCA	143279
rs552846150	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415825	ATATGTTCTAGGATA[C/T]CTATTTGCTTTTTTA	143279
rs552855332	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91423115	ACAAAGGGTTGTTGT[A/G]AAAATAGGCTGATGT	143279
rs552900369	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419389	TGAAAATATTTAACT[A/G]TATGTTAATAGCAGA	143279
rs552909179	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91454003	ATCACAAGTGTGTAC[A/G]CACCAAACAGCAGAG	143279
rs553002428	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91408849	GCAACTATATTAAAG[C/T]AGAAAGCCTTTCTAT	143279
rs553030067	snp	A/G	0.00597247	0.0543191	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409742	TCCCCGGGCTGCGCA[A/G]GCTCCGGGCCGCCTC	143279
rs553045858	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452188	ATCAGAGTCCCAGAA[A/G]GAGAGGAAAAGACAG	143279
rs553066012	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91407928	CTGTACAGAATGGCC[A/C]GAGCTCTCTGTATGT	143279
rs553077909	snp	A/C/G	0.00398564	0.0444627	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91416565	TAAGCTGTACTATCT[A/C/G]GATTTGTATAAGTAC	143279
rs553087720	snp	A/C	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91454710	ATCTCCTAATGCTAT[A/C]GCTCCCCCCTCCCCC	143279
rs553125024	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91434631	TTTTTTGTTCTTCTT[A/T]TTTTGGGACATCTTA	143279
rs553227581	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433665	ACTCTGTACATATGT[C/T]GCTTTGTTCATCTGC	143279
rs553235813	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91443987	TAGATTATATTTGGT[A/C]ATCTTTATGAAAGGG	143279
rs553280955	snp	G/T	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483833	CTTCATTTAATAGAA[G/T]TCATTGATTCATTAT	143279
rs553447635	snp	C/G	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91417155	TCTCCTTTTTTTATA[C/G]TTTTGTAGTTAACTC	143279
rs553461944	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458510	AAAGTTGAAAGAATC[A/G]GTCTACCTGGTTTTT	143279
rs553515837	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431487	TGTTTTCCAACTTGG[G/T]TCCATTCTCCCCGTC	143279
rs553672677	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91504950	GAAACCCTACAAGCC[A/G]GAAGAGAGTGGGGAC	143279
rs553676446	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496891	GAAAATTTTGAAATA[C/T]TGGATCAATTTTTCT	143279
rs553680043	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449550	TTTGGCCAGGGCAAT[C/G]AGGCAAGTGAGAGAA	143279
rs553713598	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91504314	GAAGAAGGCTTCAGA[C/T]GATCAAATTACTCTG	143279
rs553747277	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490795	ACTCGGGAGGCTGAG[A/G]CAGGAGAATGGCATG	143279
rs553785853	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91474856	GCTAGGAAGCTCAGG[C/G]AGGGCCTCTGTAAGG	143279
rs553791029	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458713	TAAACATTAACCCCA[A/G]ACTCACACCTTATAC	143279
rs553798857	snp	A/G			intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91489235	ACAGAGCATGCAAAC[A/G]AATGAGTAGACACTT	143279
rs553820923	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499854	TTTGGGGCAAAACCA[A/C]GTGGCTTACATTATT	143279
rs553851492	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91411618	TAGGAATAATTTTCG[A/G]ATTCGGTAGGTTTTT	143279
rs553857081	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478528	TTTTTCTATGCAGAT[A/G]TATATGCTTAACAAA	143279
rs553908575	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482187	AAGTTATCAGCTGAG[G/T]TCAGTCCCAGATTTT	143279
rs553934257	snp	A/G	0.0154538	0.0865337	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91455885	ATCAGATGGTTGTAG[A/G]TGTGTGGTATTATTT	143279
rs553967724	snp	A/G	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492782	AAAATTTAATTTGTC[A/G]TTGAAATAAACATTT	143279
rs554046370	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493085	CCAGATATCCTCAAA[A/G]TTAATTTTGATCATA	143279
rs554064826	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471690	CAGAGAGCCAAATCA[A/G]GAACGCAATTCCACT	143279
rs554083013	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492116	GGCAGTAGATACCAG[G/T]AGGTAGTACTTTGGG	143279
rs554143223	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91486001	CACTTTATATCCACA[C/T]TTCTAGTTTGGATTA	143279
rs554155639	snp	C/T	6.61868e-05	0.00575231	synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485211	AGTTCACCCTCCCCT[C/T]ATTCCTTATACTGAT	143279
rs554170984	snp	C/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91429089	GTTTTTAGCATGAAG[C/G]GTTGTTGAATTTTGT	143279
rs554173002	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437355	TTTTTCAGGTGGCTC[C/T]TGGCATCCTCACAGC	143279
rs554180012	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496621	GTCACTTACTAGCTC[G/T]GTGAATTTGGACAAG	143279
rs554194367	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91495554	TGAAATTTGATCTAA[A/C]ACCTCTCTTTCCATA	143279
rs554285388	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91436819	TTGGTATTTAGCTGT[C/G]TCAGGTCTACTAAAC	143279
rs554380994	snp	A/G	0.00279162	0.0372561	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412620	TCAGTACCATTGATT[A/G]TTTATTTTTTAAAAA	143279
rs554411494	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91479743	CAATACATTTTGTCA[C/G]ATTTATTTACAAAGC	143279
rs554504303	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91408925	TCAGATCTACTTGTT[A/G]CAAATTGTGGGTTTG	143279
rs554506125	snp	C/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91429948	TTTGCTCTTGTTTTT[C/G]TAGTTCTTTTAACTG	143279
rs554525876	snp	A/T	0.0103295	0.0711199	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91475536	ATAATTGATGACTTT[A/T]ATAAGAGTCTAGTAA	143279
rs554530898	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476262	GGTCAAGTGCAGTTG[A/C]AGGCAAATTGGTAGA	143279
rs554531449	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91466543	TATTCATTCAGTGCT[A/T]TACATTTCCCTCTAA	143279
rs554532328	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460943	CATATTTGAAGGACG[A/G]AGTGGGAATGATAAA	143279
rs554546044	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91465748	TTAGTTGATTTTCAG[G/T]TGTTGAACCAGACTT	143279
rs554565634	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91417246	ACTTACTCTTAAGTT[A/G]ATATTTGTAACTTGG	143279
rs554569459	snp	A/G	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433430	GGTAACTATGTATGC[A/G]TTGTCCAGAACCTTG	143279
rs554571427	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91424576	TTGCGCTTCAAAGTA[C/T]GTGTGAAGATTTTTT	143279
rs554600610	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415692	CATAGGTAATAGGGA[A/C]CATGTGGTACAAAGA	143279
rs554645926	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422662	ACACACTAGTTTTGT[A/G]TACCTGAACAAACTG	143279
rs554669364	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91474144	GAATAATAAGAAATC[A/G]AAAGTAACCTCTAAA	143279
rs554684422	snp	G/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432847	AAGCATACTGTGATC[G/T]TTGTCACCCTGAAAT	143279
rs554692090	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91486452	TATAGAGCTTCCTCT[A/G]ACAACTGTGCCACAA	143279
rs554702297	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415183	GTCAATAGCATTCCA[A/G]ATTAGAGAAAGTGTG	143279
rs554730817	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483176	AATATTTTCAGGTCT[G/T]TAGAAATGATGCTTA	143279
rs554736697	snp	A/C	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468482	GAAAGAACCAGAACA[A/C]GAACTCCGGCAACTC	143279
rs554756146	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458365	CCCCAAATTGATACA[A/G]AAAGGAACTTTATGC	143279
rs554858842	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91416468	GTGTTACAGTTGTCT[A/G]CAGTATTCAGCATGG	143279
rs554861805	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422760	CACTGTCTTACCTCT[C/T]TTTTCAATTTTCTCT	143279
rs554890604	snp	C/T	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91434516	TATAGAATGAGGAAA[C/T]TGGGCATCTTGAGTC	143279
rs554906055	snp	C/T	0.000281889	0.0118687	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425444	TATTTTGGCTAAAAG[C/T]ATATTTTTAAATTAT	143279
rs554938019	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91480515	AGAATGTACCAAATA[C/G]ATCTTGAGCAGGCAA	143279
rs554940305	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91434320	AAGCAGTCATAAGCA[A/G]TACCAAAGTACTAAA	143279
rs554950988	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91456745	TATTATTTTGAGATA[C/T]GTCAAAAAGGGGGAA	143279
rs555017642	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91465027	CATAGTAGTTTAACT[A/G]TATAATCCTAACTAA	143279
rs555035718	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419576	CGTTTTTCTGCTGTT[G/T]GCAACGTTTATTGAA	143279
rs555056582	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91424161	CACAGTCGAGGAAAA[G/T]AGAGAAGAGCTAGAG	143279
rs555096276	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91448854	TCTCTGAATAGACCA[A/C]TAACAAGTTCTGAAA	143279
rs555101064	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439706	ATATTGATTCTTCCT[A/G]TCCATGAGGATGGAA	143279
rs555126688	in-del	-/TCA	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502570	TCAATAGTATTTATG[-/TCA]TCATCAAGATTATAT	143279
rs555154537	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420289	TGATTACAAAAAAAA[A/G]AAAAAAGAAAATCAG	143279
rs555157659	snp	A/T	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91455405	ATATCCTTCACCCAC[A/T]TGTTGATGGGGTTGT	143279
rs555170735	snp	C/T	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503366	TTCCATCTGAGGTAC[C/T]GGGTTCATCTCACTA	143279
rs555214149	snp	C/T	0.0248432	0.108648	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458017	AGATGGCATAATTGT[C/T]TATGCAAAAAAAAAA	143279
rs555225486	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91436916	GTCCTTATAGACTTA[C/T]ATCTTTAAAACAACA	143279
rs555275702	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91455060	TTTATAGCAGCATGA[C/T]TTAAAATCCTTTGAA	143279
rs555288864	snp	C/G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445839	CTGTGCCCTGAGGAA[C/G/T]GGTGCACTCCGGCCC	143279
rs555337147	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471627	AAGTTTCTGAATGCA[A/G]AATCAATATATAAAA	143279
rs555337365	snp	A/T	0.00914312	0.0669923	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509290	TAAAAAAAATAAATT[A/T]AAAAAAAAAATCAAA	143279
rs555365072	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470261	AAAACAACAGAATAC[A/G]CATTCTTCTGAACTG	143279
rs555375146	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91411356	TTTGAAGCACAATTT[A/T]AAAAAAAACCTCGGA	143279
rs555429377	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444060	GTCATCTCCTCTCTT[C/G]AACACCAGTCTTATT	143279
rs555502961	snp	G/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91505005	TTTCAACCCAGAATT[G/T]CATATCCAGCCAAAC	143279
rs555506108	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91427772	CAGATGAGTAGGTTG[C/T]GAAAATTTTCTCCCA	143279
rs555527947	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500795	TAATATGAAATCACT[C/T]CCTTTGGGAGAAAAT	143279
rs555545970	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91506370	AACAAAATTGATAGA[A/C]CGCTAGCAAGACTAA	143279
rs555614554	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439005	TGGATAGATTGCAAA[A/C]ATTTTCTCCATTCTG	143279
rs555619044	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426676	ACTCCATTATTTCTA[C/T]ACTAATATCTTCATC	143279
rs555680880	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477673	TGTATTGGCATTTGC[C/T]TCTTTCATGTAACAT	143279
rs555722638	snp	A/G	0.105924	0.204309	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91506253	TCAAAAGCTAGCAGA[A/G]GGCAAGAAATAACTA	143279
rs555785762	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497980	AAATCATTAACCATT[A/T]TGTGCCCTGGAAAAT	143279
rs555789419	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91473355	TTGATTGATGTAGCC[A/G]GAGAAACTGACTTTC	143279
rs555846244	snp	A/G	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91511986	GCAGAATTCAAATTC[A/G]TATCTGTCTGACTCC	143279
rs555852121	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409559	CAGTCAAAGAGGGAC[A/G]AGAGGAACAGGAATG	143279
rs555878122	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503252	TATTGTTATATTAAA[A/T]AGTCAAAAAATGAGG	143279
rs555882246	snp	C/T	0.030278	0.119257	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91429272	ATGTGCTGCTGGATT[C/T]GGTGTGCCAGTATTT	143279
rs555907862	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91423376	ACTGTAGTAGTAGGT[A/G]TATAACAAGTACTCA	143279
rs555925989	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91495057	AAGTTAAACAATTAA[A/T]TCTAAAAATTATAAT	143279
rs556007059	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91435752	TGTGCTATATACTCG[A/G]TCTAGCAGCTTCATG	143279
rs556034190	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422807	TAAATCCACTAGACA[G/T]TAGAACTGATAGTTG	143279
rs556035413	in-del	-/CAA	0.00119784	0.0244435	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91469953	AACAGACTTTTAAAC[-/CAA]CAACAATCAAAAAAG	143279
rs556089163	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487583	ACACAATCCAAAAGT[A/C]ATGTTTTATATTGCT	143279
rs556120389	snp	C/T			intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91463999	TGAATTTAAGTCGTT[C/T]TTTGCAAACTAAGAA	143279
rs556136285	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91480886	CTAGTTAGCTCAGTC[C/T]TTAGTTATCTTCAGA	143279
rs556137768	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91494408	GTGAGAATAAAAAAG[G/T]CTAAATTGTGCTGGG	143279
rs556152656	snp	A/C	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491970	CTACCTCAGCCTCCC[A/C]AATAGTTGGGATTAC	143279
rs556152935	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502558	ATAGCTATTTCTTCA[A/G]TAGTATTTATGTCAT	143279
rs556164228	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432041	CTAGCTGTTCTATCT[C/G]GATGCCACCTGAATT	143279
rs556191152	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490823	ATGAACCCAAGAGGC[A/G]GAGCTTGCAGTGAGC	143279
rs556316926	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91472598	CTATAAAAAACTGAA[A/G]TAATAAGCAAAAGCA	143279
rs556339092	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449573	TGAGAGAAATAAAGG[A/G]CATTTAAATAGGAAG	143279
rs556391414	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484850	AGCTTTATGTCTTTT[A/G]GTGGACAGTGTTCTG	143279
rs556402022	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483244	CTTTAGTACTACATA[A/G]AGGATAATTAAAAAT	143279
rs556441075	snp	C/T	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91465311	ATGGTTTTTAATAGA[C/T]GTAGATACATGTGTG	143279
rs556469106	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482415	CATTTAAAAGTTGTC[A/G]GAAGCTGTATGTGTT	143279
rs556565210	snp	A/C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420802	CTGATTGACATACTA[A/C/G]GAAGCATCAATGTCC	143279
rs556583886	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91506278	TAACTAAAATCAGAG[C/T]AGAACTGAAGGAAAT	143279
rs556593437	snp	A/C	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91486176	TAAACTTTCCAGGGA[A/C]CCTCTTTATCAGAAT	143279
rs556601236	snp	A/G	0.0107246	0.0724382	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91430101	TCTTGTTGGTTTCAA[A/G]GAACATCTTTATTTC	143279
rs556677960	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91454202	CATTTACAGCACGCT[C/T]TACTCAACAACAGAA	143279
rs556702177	snp	A/T			intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91407832	TCCTAGTTTTTCCAA[A/T]GCGAATGAGTTTATA	143279
rs556739859	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464728	TAGTTGGAGCACACA[C/G]CATGCTACCTGTGCA	143279
rs556758030	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91469435	TCAAGACAGAAGAGA[C/T]TGGGAGCCTATATTC	143279
rs556775781	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425514	AGGTCTAGTTAATAC[A/C]ACAAAAAGAAGCTGT	143279
rs556786208	snp	A/T	0.00438332	0.0466095	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433544	CATTGTATTGGATGT[A/T]CATTTGTATTGAAGT	143279
rs556828715	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91413938	GAAGTAATGTATGGA[C/T]ATGAAGGGCTGATGA	143279
rs556848598	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431851	TAGCTCGGAGTAGTT[G/T]GATTGTCTGAAGCCT	143279
rs556852637	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471819	ATTACAGATGAACAA[A/G]CAAATGGTAAAACAT	143279
rs556890334	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425922	AAATGGAAAAAATGT[A/T]CATTATTTATAGTAG	143279
rs556945388	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91469922	GAGCAGGGATTGTTA[C/T]TGCAACTTCAGACAA	143279
rs557007049	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468640	AAGTAGAAGCCCAAT[A/G]TAAGGAATCTAAAGA	143279
rs557026179	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91417419	GTACATGTGCACAAC[A/G]TGCAGTTCTGTTACA	143279
rs557029778	snp	C/T	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91416286	GAAATGAAGTCTAAA[C/T]TAACACACATAAAAC	143279
rs557035237	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458444	ATTATTTTCAGATTT[A/G]CCTGGAAAGGCGGAA	143279
rs557042074	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415328	ACAAGAGGTGAGATG[G/T]GAAAGAATGAATGCT	143279
rs557080392	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461213	AGTTTATCTGAATAA[C/T]ATTTCTATATGTATA	143279
rs557100531	snp	C/T	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467299	CTCCAGCCTGTGTGG[C/T]GCCCAGATGGTTTGG	143279
rs557103630	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91443274	TGGGGTTTTTGTGTG[A/G]ACATCCTTTTTGTTG	143279
rs557108429	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91407795	CTGGACTTAGAAACA[C/T]GAAATGCTTCTTCTG	143279
rs557113149	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438505	ATTTGGGTTGGTTCC[C/T]AGTCTTTGCTATTGC	143279
rs557149121	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91453101	AAACAAAAATTATAA[C/T]ACCAGCGTGGTTCTA	143279
rs557214029	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451998	GAGAAAATACAACAA[G/T]CAAAGTAAAAAGCTT	143279
rs557263867	snp	C/T	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496774	TTTAAAGGAATAGAA[C/T]ATTTATTATGTAAAA	143279
rs557331446	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91446156	GCAGGTGCCCCTCTG[C/G]GACAAAGCTTCCAGA	143279
rs557344747	in-del	-/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438091	CTGACTTAAGCCATC[-/T]TTTTTTTTTTCTTTA	143279
rs557385682	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412421	GTATGAGTTGGAATA[C/G]AAGAGGATAAGGATA	143279
rs557392740	in-del	-/T	0.00358779	0.0422022	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420289	GATTACAAAAAAAAA[-/T]AAAAAAGAAAATCAG	143279
rs557447452	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91411423	CTTTTTGAAAGTTTG[C/T]TTTGATATATTTAAA	143279
rs557464813	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91466714	AAAAACCTGCACACA[A/C]ATGGTTACAACAGCC	143279
rs557504334	snp	C/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438188	CCTGCACCCATCAAC[C/G]CGTCATCTACATTAA	143279
rs557522906	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432463	TAGGAGTTTTACCTA[C/T]TGTAACAGCTGCTAG	143279
rs557598995	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503695	GGCGGCAGCGAGGCT[C/G]GGGGAGGGGCGCCCA	143279
rs557618252	snp	G/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437642	TTTTTTTTTTTTGGT[G/T]GTTTTGTTTTTTTTG	143279
rs557618302	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449513	CCTCTCTTACTACTC[C/G]TATAAACATATTATT	143279
rs557679773	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449102	CAGGCCAATATCCCT[C/G]ATGAACATGGATATG	143279
rs557691612	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91515265	GGTTTTCGCAGGAGG[G/T]GACACAAGATCAGTT	143279
rs557693257	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91455485	GAGCCATTTGTCAGA[C/T]GAGTAGATTGCAAAA	143279
rs557731878	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503225	ATACCATCTCACAGC[A/G]GTCAGAATGGCTATT	143279
rs557759311	snp	A/G	0.0111196	0.0737302	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509026	AACTATCGCAATAAC[A/G]AAAAACCAAACACCG	143279
rs557794467	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91515304	TGGCCGCAAATCGTT[C/T]AGTCTAGTGCCTAGG	143279
rs557796524	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91506336	TAATGAATCCAGGAG[C/G]TGGTTTTTTGAAAGG	143279
rs557811606	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91456459	TGAAGTTGCTTATCA[A/G]CTTAAGGAGATTTTG	143279
rs557860719	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91488494	TTGTTTAAGTGCTTA[C/T]GTATTTCAAACATCT	143279
rs557891536	in-del	-/TATGTTCATACATATATGT	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91494809	ACTATGAGCTATTTA[-/TATGTTCATACATATATGT]TTGTCATGCTTTATA	143279
rs557897460	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499205	TGTAGTACTATCATG[G/T]TAACAAATAATTAAT	143279
rs557920676	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471041	AAAACCTCAGGCCAA[C/T]ATTCCTGATGAAAAT	143279
rs557926597	snp	A/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492058	AGGGGAGTTTTTTTT[A/T]AAAAAAGAAATGAAT	143279
rs558049885	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460676	ACTATAAGATATTAG[C/T]CAAGAGGACCTCAAA	143279
rs558053843	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500852	TAGAGATTTTACTTT[A/T]AAAAAAATGACTTTG	143279
rs558055691	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91511647	ATAAGGGGCATGCAA[A/C]CTAGATTCCTTGCAC	143279
rs558092661	snp	A/G	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91510221	GGGCATGAATCCTTG[A/G]CAATATTTTGTGGTT	143279
rs558124678	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440442	CAACTTGATTGTGGT[A/G]GATAAGCTTTTTGAT	143279
rs558126761	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499801	TCTTTCATTTGAATT[A/G]TTTTTCATGGGAGAG	143279
rs558154060	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445768	GGCTTTGCCACATCC[A/G]GGAAGCACAAGGGAT	143279
rs558162454	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503632	GGAGGGTCCTACCCC[A/G]CGGAGTCTCGCTGAT	143279
rs558201635	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503326	TCCCAGCCTGAGCGA[C/T]GCAGAAGATGGGTGA	143279
rs558263244	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91495414	TTGAAATTTTGGTGG[C/T]CTTCCAATTTTTAAA	143279
rs558269402	in-del	-/A	0.00557542	0.0525036	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498780	TTAGAAGGAAGGGGG[-/A]AAAAAACTGTTTTTT	143279
rs558380188	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91479561	ATGTCTGACTAATAA[A/C]TTAGAATAGGAATGT	143279
rs558423960	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91428919	CCAACACTATGTTGA[A/C]TCGGAGTGGTGAGAG	143279
rs558534161	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471956	ACAGAATTAGGAAAA[A/C]ACTATTTTAAAATTC	143279
rs558539472	snp	A/C/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484984	CTCACCACAAGTTTT[A/C/G]TTTTTTAAGCAAGAA	143279
rs558546601	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422555	AGCCCCAGTCATTAA[C/T]AAAATTCTTATTTAA	143279
rs558557025	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91494543	ATAAATTATGAGACA[G/T]ATATATGGAAACTGA	143279
rs558609325	snp	C/T	0.00438332	0.0466095	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445801	GAGAAATCCCTCCCC[C/T]AGCCAAGGGAAGTCG	143279
rs558657117	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419991	TCGTATTAAATACCC[A/G]GTAACTTCTTGATTT	143279
rs558698902	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461613	GAATGCAGTGGTGCA[A/G]TCTCAGCTCACTGCA	143279
rs558715123	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422459	CTTTCTTATAACTGT[C/G]AAATTTGTGTGTCCA	143279
rs558737650	snp	G/T	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492999	TTTTCAGTGTTTTCC[G/T]TATTCTTTAGTTTTC	143279
rs558748085	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91466288	CTTTCATTTAGTAAT[C/T]AGTATTTTCTCACTT	143279
rs558770921	snp	A/T	0.00199481	0.0315187	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512893	ATATACTGGCTTGGG[A/T]CCTATAAGATTCTTC	143279
rs558775604	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467367	CCATCCCTCAAGGCT[C/G]ACTGTGCTCCTCCTG	143279
rs558792044	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91475402	TTAGATGGATAAGGC[A/C]TTCGTGAAGGAGAGA	143279
rs558795869	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483248	AGTACTACATAAAGG[A/C]TAATTAAAAATCTGT	143279
rs558802372	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91411493	AAAAGTTTAGTGAAC[A/G]TTATACATTTTCTTT	143279
rs558843270	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457786	TATTCAACATGGTAA[A/G]AATCAAAGGGAGTAC	143279
rs558856016	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91465679	GTTTCTTTTGCATCT[A/G]TTGCTATGATCCCAT	143279
rs558888783	in-del	-/GAGA			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91488233	GTGTCTTGGAGAACT[-/GAGA]AATATGCCCAAAGAA	143279
rs558900320	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432745	TACCTTGAGAGCAAG[C/T]TCATAGCCAGCTCAG	143279
rs558922119	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438732	CTCCACATCCTCTCC[A/G]GCATTTGTTGTTTCC	143279
rs558960883	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445874	ACTACACTTTTTCCA[G/T]GGTCTTTACAACCTA	143279
rs558988026	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468018	CAATGCCACAAGCCC[A/C]CTCCTACTAGTACCT	143279
rs559007316	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421830	TTCTGAAATTTGAAG[A/G]AAGCATTTTACATTG	143279
rs559019235	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91413477	ATGCACAGTAGAATT[A/T]ACTGAGAAACTTTTA	143279
rs559079103	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452437	TTTGAGTATTTATTT[C/T]CACCAAAATTCATGT	143279
rs559114303	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451562	TGCCCCACTCCAGAC[C/T]TACTGAATCACAAAG	143279
rs559207539	snp	A/G	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91505308	GGACTAAATGCTCCA[A/G]TTAAAAGACACAGAC	143279
rs559245171	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91504640	TGTGAAAAGACCAAA[G/T]CTACGTCTGATTGGT	143279
rs559298534	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500742	ATATTAGAGAGTCCC[A/T]CAGTCTTATTTTATC	143279
rs559337675	in-del	-/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91513573	AGTCAGACAGTAAAT[-/G]TTTTTTTTAATTTAC	143279
rs559412002	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91417520	ATGCTATCCCTCCCC[A/G]CCCCCCCACAACAGG	143279
rs559479035	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409155	AAAATCTGATAGAGC[C/T]GAATATCGAAATTCC	143279
rs559582286	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439567	TCTTGGCTATACAGG[C/G]TCTTTTTGGTTCCAC	143279
rs559658732	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432940	GATCTTCACAGGTCA[A/G]GTACTCCAGAGTTTT	143279
rs559674579	snp	C/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91429327	TCATCAAGGATATTG[C/G]TCTAAAATTCTCCTT	143279
rs559735124	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91475967	CACTCTCTTTTCTTT[C/T]CTGCTAGTGCTTTCT	143279
rs559769544	snp	A/T	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485644	AATATTTTCAACACT[A/T]TAGGTTACACAGGTT	143279
rs559783764	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91515301	AGATGGCCGCAAATC[A/G]TTTAGTCTAGTGCCT	143279
rs559835516	snp	A/G	0.0325976	0.123435	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503738	CTTGCTTAGGTAAAC[A/G]AAGCAGCCAGGAAGC	143279
rs559861232	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425744	GAGCAATAATCAATT[A/G]GAAGACTTTATGGAA	143279
rs559870412	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503540	CTGGAAAATCGGGTC[A/G]CTCCCACCCGAATAC	143279
rs559875417	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476492	TTGAAGACATTGAGC[C/G]AGACTAAGAAGCCTC	143279
rs559887648	snp	A/C			upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409460	GGAAAGGAACAAGGA[A/C]GGGACGGATAGGAGA	143279
rs559956460	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91510798	AATGTATGTCTGGTG[C/T]GTAAAAAATTAAGAA	143279
rs559987583	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91414816	GGAAGCATGCTGGGA[A/G]CTTGTGGGAGGTGAG	143279
rs560014002	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420812	TACTAGGAAGCATCA[A/G]TGTCCATCATGCCAA	143279
rs560046103	in-del	-/C	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91473412	TAAAATAAACAAAAA[-/C]TGCCTTTACCACCAA	143279
rs560065060	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91472335	GACTTTAATGTAAAA[A/C]CTGAAAGTATAAAAA	143279
rs560068820	in-del	-/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91465560	ATGTTAGCTGTAGGG[-/T]TTTTTTTTTTTTTAA	143279
rs560099165	snp	C/G	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91495925	TGTAAAATAATTACA[C/G]GCAAGTCTTAAGTTG	143279
rs560127108	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481291	CCAGAAGATTTTTTT[A/T]AAAGTAGGATTAATA	143279
rs560194660	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509546	CTATTCACAATAGCA[A/G]AGACTGGATAAAGAA	143279
rs560257919	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452683	TCAGGACTTTGCAGA[A/G]TCCCTGTTAGCAAGA	143279
rs560266947	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460045	AAGCAATGTGTGACT[A/G]TGTTCAAAAAGCTAA	143279
rs560267394	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412874	GTGTGGGGAGGGGGA[A/G]GAGGTCTTGATGTGT	143279
rs560270452	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91472912	TTAGTAAACTGGAAG[A/G]TAGAAGTGAAGAAGA	143279
rs560360613	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91418744	AGTCTCTTTGTAGAC[C/T]GTAAATTATATCGTT	143279
rs560365580	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464537	CCTGCCTTGGCCTCC[A/G]AAAGTGTTGGGATTA	143279
rs560408471	snp	A/G	0.00716266	0.059414	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450710	CAAAAAGTGGGCAAA[A/G]GATATGAACAGACAC	143279
rs560468578	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491475	AAGTTTGATACCATA[A/G]TTAAAATCAGATCTG	143279
rs560484825	snp	A/C	0.000798881	0.01997	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91469952	AAACAGACTTTTAAA[A/C]CAACAACAATCAAAA	143279
rs560515697	in-del	-/ACTT	0.00755907	0.0610114	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500983	ACTATCCACTGCTGA[-/ACTT]ACTTATATACTTTTA	143279
rs560546819	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91428018	GTTTTAGGTCTAACA[C/T]TTAAGTCTTTAATCC	143279
rs560574092	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477904	TTACTCTGTCCTGTC[A/G]GGTCAAGGAAAGTGA	143279
rs560606644	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91436029	GAATCTTTCTTTTTT[A/G]TAGTACCCTTTTATT	143279
rs560608944	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91427071	TGTTCTCATTGTTCA[A/G]TTCCCATCTATGAGT	143279
rs560731349	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461537	ATATAAGTATATGGG[G/T]TTTTTGAGGGGGTTG	143279
rs560733379	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470719	AAGAGTTCCATCCCA[A/G]GATGGAACCAGGAAG	143279
rs560733837	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91474877	CTCTGTAAGGCAACA[A/G]TTGAGGTCTTAATGA	143279
rs560852517	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452384	AAAGATCTTGAAAGC[A/C]GCCAGGAAAAAATGA	143279
rs560923373	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490848	GTGAGCCGGGATAGC[A/G]CCACTGCAGTCCAGC	143279
rs560944405	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91423744	TTTATTCTCTTTGGG[A/C]TCTTTTATATTAATT	143279
rs561007802	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432316	CCGTCTGATCTTCAA[A/G]TGATATTAGGGAAAC	143279
rs561011684	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464843	CTCTCTGAGTTCTTT[A/T]GACTTGGAATATTAA	143279
rs561012740	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91473656	AGCCTACTTAATGTG[A/G]AGATAAAGAGGATAA	143279
rs561022558	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91414903	TTTTTCCCCCTGCGG[C/T]TAGTGGGAAGCTATT	143279
rs561034481	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91407463	GGCTAAAATAATTTC[C/T]CCAAGTTTACTTTAG	143279
rs561065332	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458726	CAAACTCACACCTTA[C/T]ACAAAAATAAAGTTA	143279
rs561088474	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451003	TAACCTAGCAATCCC[A/G]TTACTGGGTTTTATC	143279
rs561132990	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482749	GGTAGAATTAGCCCT[C/T]AGACCCAGATCTGTC	143279
rs561133304	snp	C/T	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91494741	TCTGCAGTAATCATT[C/T]GTTGAATGTTTCATC	143279
rs561172027	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493685	ATGTCAGTAGACTTA[A/C]TTGAAAGAAATGAGA	143279
rs561201030	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467429	TGGACAGAGTAGGGT[A/G]GTCTTGCCTGTGAGA	143279
rs561201649	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458105	TGGTTGAAGAATACA[C/T]GATAAACATACAAAA	143279
rs561216776	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91514968	ATGAAATGTATATCC[A/G]ATATTTGAAAGATCA	143279
rs561236762	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91413536	GTATTGTTAAATCAG[A/C]ATTTCTGGGGATGTT	143279
rs561248322	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502252	CTATGCTTTAGTCAA[C/T]AGGCTGTTTGCTGGT	143279
rs561307092	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91454083	AAAATCCACAATTAG[A/G]TATTGAAGTCTCCAA	143279
rs561326766	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449798	GCAAAGATAATAAAA[C/T]ACCTAGCAATACAAC	143279
rs561341588	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439257	TTAATTTTTGTATGA[C/G]GTGTAAGGAAGGATT	143279
rs561369730	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91453317	ATGCCTGTAGTCCTA[A/G]CTACTCAGGAGGCTG	143279
rs561481989	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460664	AACTTTTGGATCACT[A/G]TAAGATATTAGCCAA	143279
rs561483407	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444350	GAGCCTGAGAGTGGA[A/G]AGATTCTTACATAAG	143279
rs561528869	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478074	AAAATCAGTACTACT[A/G]TAAGTGTCAGTCCTG	143279
rs561548455	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91459492	AATACTATTAAGCAA[C/T]AAAAATGAACTATCT	143279
rs561572462	snp	A/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91505777	ACCAAGCAGACCTAA[A/T]AGACATCTACAGAAC	143279
rs561648022	in-del	-/CT			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91418204	AAAAAAAGAACAAGA[-/CT]CTTAATTGATTGAGA	143279
rs561653529	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438610	TAATGGGATTGCTGG[A/G]TCACATGGTATTTCT	143279
rs561702611	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425158	AGTCAAATTTATATA[C/T]GTTTTTATCTATTAT	143279
rs561830453	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409847	GAAGGCGAAAGGCCA[A/C]CAGCCCAGACCCCGA	143279
rs561835264	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91428145	GGGAATCCTTTCCCC[A/G]TTGCTTGTTTTTCTC	143279
rs561880281	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91435547	AACATTGCTAAATTT[C/T]AGGCCACTCAGTTCC	143279
rs561913866	snp	A/T	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91418438	TGATCAATTGCGTTG[A/T]TTTTTTTTTGTGACA	143279
rs561945428	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91459844	GTATTACAGTTGTCT[A/G]CAGTATTCAGTACAT	143279
rs561960505	in-del	-/GT/TGTGTGTGT/TGTGTGTGTGT/TGTGTGTGTGTGT	0.0733725	0.182611	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415193	TCCAAATTAGAGAAA[lengthTooLong]GTGTGTGTGTGTGTG	143279
rs562021643	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91506737	TGAAACTATTCCAAT[C/G]AATAGAAAAAGAGGG	143279
rs562026930	snp	C/T	0.00318978	0.0398085	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91417566	TTCCCTTTCCTGTGT[C/T]CATGTGTTCTCATTG	143279
rs562042936	snp	A/G	0.00318978	0.0398085	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503846	GACAAACAAAAAGAC[A/G]GCAGTAACCTCTGCA	143279
rs562062427	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445187	ACCCGACAAAACAAA[G/T]ACTGACATTTTGAAT	143279
rs562063353	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433030	GCTATTTGTGGAAAG[C/T]AAAGGACTTGCCACG	143279
rs562070011	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440431	AGGGATGAAGCCAAC[G/T]TGATTGTGGTGGATA	143279
rs562086258	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425976	AGTTAACTAAATTAT[A/G]TTAATCTATACTGCA	143279
rs562093127	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485714	ATGTAAATGAATAGA[C/T]ATGTCTGTGTCCCAA	143279
rs562110409	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409232	AGATCAGCAGGTGTC[C/T]CCGCCGCTCCAGTAG	143279
rs562114804	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421162	CCACCATTACCCTAA[A/G]TCTGTTACCTCAGCT	143279
rs562128205	snp	C/T	0.000873398	0.0208791	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496318	TCCTAGTGATCAAAA[C/T]ATACCAGTAGGCATC	143279
rs562129530	snp	A/G	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91443512	CCTGTATGTGGTGTT[A/G]GTCAACCCCTGCTGG	143279
rs562153100	snp	C/T	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468102	ACATGCAAGCAAGCA[C/T]GGATCCAACTGCCAC	143279
rs562175864	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91504462	TGAAAACCAAGGCTC[A/G]AGAACCACGTGAAGA	143279
rs562187761	in-del	-/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501779	CTAATACTAATCCTC[-/T]TTTTTTTTTTAATCT	143279
rs562307445	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468847	AGGCTTTAGTGGGAG[A/G]ATCACTTGAGCCCAG	143279
rs562319577	snp	A/G	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476980	GGTCAGGAGATCGAG[A/G]CCATCCTGGCTAACA	143279
rs562338923	snp	C/G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91456920	GGCTCTTTGACAAGA[C/G/T]CAGTAAAATTGATAA	143279
rs562414427	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421227	GCACATTTTAGACCT[A/G]ACCACTCTTCATTAT	143279
rs562428802	snp	A/G	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502127	AACACTATTTAGATC[A/G]TATTTCCGTGGGAAA	143279
rs562502927	in-del	-/AC	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91407955	ATGTCCTGCTTTACA[-/AC]ACTCTCTTCTCCCAC	143279
rs562524713	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91456561	TTCCTAATTGAATAC[C/G]CTTTATTTCTTTCTC	143279
rs562574311	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91459232	TGAGTATGTAGAGAA[A/C]CTGGATCACTAATAT	143279
rs562588226	snp	A/G	0.00438332	0.0466095	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91430526	TCTAAGTCTCTTTGT[A/G]GGTCACTCAGGACTT	143279
rs562608571	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501046	TCTAATACGTATATA[A/G]AAGCTCACCATTCCT	143279
rs562647159	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437782	TTCTCTATTACAGGC[C/T]GTTATCTAGGTCACA	143279
rs562725943	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431239	TTGTAGAGTTTCTGC[C/T]GAGAGATCTGCTGTT	143279
rs562759075	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91486704	TAAAACTAATATATA[C/T]CTTACTGAGTTCATT	143279
rs562791438	in-del	-/AG	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91453455	AAGAAAATTATAAAC[-/AG]GGGATGGTAAGGGAG	143279
rs562791795	snp	G/T			intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462586	TTGGGTGAAGCCCAA[G/T]AATTTTCATTTGTAA	143279
rs562869524	in-del	-/T	0.00358779	0.0422022	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91495736	AATAGCATGTTTATA[-/T]CCATATGTTTATTCA	143279
rs562870456	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91411838	CTGGTTCCTGCTGCT[A/G]GTACCCTAGGTTTTC	143279
rs562911958	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470775	AATGAGCTCTGAAAT[C/T]GAATCAGTAAGAAAC	143279
rs562920510	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503547	ATCGGGTCACTCCCA[C/T]CCGAATACTGCGCTT	143279
rs562926826	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501450	ATTTTCATAGAAAAA[G/T]CTTCAGAGTAAACAT	143279
rs562932213	snp	C/G			intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462365	TTATTTTTTAATTAT[C/G]AATTAAGCAGCAAAT	143279
rs562951436	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419977	TCTGGAGTTTGGTGT[C/T]GTATTAAATACCCAG	143279
rs562962713	snp	A/C	0.00318978	0.0398085	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439581	GCTCTTTTTGGTTCC[A/C]CATGAAACGTAAAGT	143279
rs562989472	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91466573	AACACTGCTTTTGCT[A/G]TATCTCACAAATTTT	143279
rs563013325	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91475741	ACAACACACTCAAAT[G/T]GGTAAATTGGGTTAT	143279
rs563013909	snp	A/G	0.00398564	0.0444627	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91429238	GAAGCCCACTTGATC[A/G]TGGTGGAGAAGCTTT	143279
rs563029226	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449180	AAAGCTCATCTACCA[C/T]GTGAGAGAACTTACC	143279
rs563076373	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91463405	GTCTCAGGTGGCAGA[A/G]GTGAAAGAAAATAAT	143279
rs563099130	snp	A/G	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91455930	CTGTTCCATTGGTCT[A/G]TATCTCTGTTTTGGT	143279
rs563133242	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458784	TTATTGGACTTTTAG[A/G]AAAAAAATGAAACGA	143279
rs563138823	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91511023	GCATGTAAATGCACT[C/G]AGCACAGTGATTATC	143279
rs563147292	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467510	CCTCAGCCTCGCCAC[A/C]CTCACTTGCAGTGCA	143279
rs563189081	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91504499	AAGCCTCAGGAGCCA[A/G]TGCGATAAACTGGAA	143279
rs563211542	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91455123	TGGTATTTCTAGTTC[G/T]AGATCCTTGAGGAAT	143279
rs563223245	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503921	CTCCTAGTACGCAGC[C/T]GGAGATCTGAGAACA	143279
rs563292057	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467961	CCCACCAGCACCCCA[A/C]ACCTACCACACCACC	143279
rs563388317	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91407587	TGACCTGTGCACCTA[A/T]TTTGCTATTGTTCAC	143279
rs563493816	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452345	AACATCATAATTAAA[C/T]TTGTCAAAACTGAAG	143279
rs563496048	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440468	TTGATGTGCTGCTAC[A/C]TTTGGTTTGCCAGTA	143279
rs563523433	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485452	AATATCATATTTATT[A/G]AAGTATTTTCTTTTT	143279
rs563523492	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91474983	GAGAAGGGAACACAA[C/T]TGGCAAATTCAGAAA	143279
rs563543382	snp	C/T			upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91408976	ATGATGCACCATAAC[C/T]AGTATTTAGTTATAC	143279
rs563555501	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449621	GTTTGTAGATGACAT[A/G]ATTGTATATTTAGAA	143279
rs563589000	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91474217	GGGAATGGGAAAAAG[A/C]AGCATTAAAAAGTGA	143279
rs563604942	in-del	-/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440656	CAGGTGGAATGGTAA[-/C]AGCTCCTCTTTGTAT	143279
rs563661631	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439352	CTTTCCCCATTGATT[A/G]TTTTTGTCAGATTTG	143279
rs563663641	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457397	ATATCCCTCATGAAT[A/G]TAGAGGCAGAAGTCC	143279
rs563746993	snp	C/T	0.00279162	0.0372561	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502971	ATAATAATGGTATGC[C/T]TCAAAAGACAAGGAC	143279
rs563755988	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91513102	GGATTCAAGGTTATA[G/T]TCTTTTAAGTGTTGT	143279
rs563760821	snp	C/T	0.00557542	0.0525036	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445222	CACATGATTAGGGGA[C/T]TGATAACTGTTCCTG	143279
rs563894146	snp	A/C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439503	TTGTAGTATAGTTTG[A/C/T]AGTCAGGTAGTGTGA	143279
rs563946209	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91454898	TACAAAGGACATGAA[C/T]TCATCCTTTTTTATG	143279
rs563981794	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91479275	ATATATCTCAAAGAT[A/G]GTGACTGGATTTGCT	143279
rs564058941	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431786	ATATATTCTTCTAAA[A/G]TTTTTTCAAAGTTTT	143279
rs564098119	snp	A/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91430359	ATGTCTATTCTGTTG[A/T]TTTGGGGTGGAGTGT	143279
rs564104636	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91417613	GAGTGAGAACATGCG[C/G]TGTTTGGTTTTTTGT	143279
rs564113539	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509352	AAGAGAATGCTTATA[C/T]ACTGCTGGTGGGAAT	143279
rs564152257	snp	C/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91507076	ACAAAATTCAACAAC[C/G]CTTCATGCTAAAAAC	143279
rs564159181	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490934	AGAGATGAGACATAC[A/G]GAAACTGTGATGCAA	143279
rs564199270	in-del	-/A	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421127	TTCATTTGTCAATTT[-/A]TTTTGTATAGTCCGT	143279
rs564231062	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91489187	AAAGAAGGAGAATGG[C/T]AGGTGTAGACTCTGT	143279
rs564248378	snp	A/G	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91505190	AATGTAAAGACCATC[A/G]AGACTAGGAAGAAAC	143279
rs564368228	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410855	GGGCTTGGGCCCCCA[C/T]TTTCTCTAAGAGAAT	143279
rs564373172	snp	A/G	6.61627e-05	0.00575126	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462073	ATGTTGAATATACTT[A/G]ATTCTTAAATTGAAT	143279
rs564377229	snp	C/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91489922	TTAATCTGCACAATA[C/G]TTTTCATTGTTACCA	143279
rs564391074	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91473687	AGACCTTTATGATAA[C/T]TGCTTCCACTTAATA	143279
rs564395141	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91486594	TCTGGCCATGAGCAG[C/T]TTCATCTGTTCATTT	143279
rs564409405	snp	A/G	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426167	AGAGGGGTGCTTACC[A/G]ATCTGTTAATGGTTT	143279
rs564414407	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500126	CTATAACCAAGTGCC[C/T]AAACTCTACAGTGCA	143279
rs564429716	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409931	AGTCTGTGCCTACGT[C/T]CTGCCCTACTGGTAC	143279
rs564449923	snp	C/T	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91418679	ACTGTGAAAAAAAAC[C/T]ATACAAAAAGAGAAA	143279
rs564470121	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433808	TGGTGCATGTAGTCT[A/G]TACTTAGTTAATAAT	143279
rs564479437	snp	C/T	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426888	AAGTTTTAGGGTACA[C/T]GTGCACAATGTGCAG	143279
rs564515245	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476610	CCGCAGGCATCCGGG[A/G]AGGAGTGCCAAACGG	143279
rs564521553	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91453515	GTAAAATGACGATAT[A/G]AGTAGCATGTGATAA	143279
rs564539295	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91436839	GTCTACTAAACCAGT[G/T]TTCACTGACATCTCT	143279
rs564571170	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467670	ACCTCCCCTCCGTAG[C/T]TTTGCCAGCATGCAT	143279
rs564574621	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498290	AACAAGGATTAACCA[A/G]TACATACAATCCTCT	143279
rs564584025	snp	C/T	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503682	GATCAAACTGCAAGG[C/T]GGCAGCGAGGCTGGG	143279
rs564620207	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444171	ACTTTTTCCCAACCT[C/G]GCTATAAACACCTAC	143279
rs564698268	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461441	CTCATTTTCTACCCA[A/G]TATTGATTTAAACAT	143279
rs564701763	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422921	TTATTAAGAAGAGGT[A/G]AAGGAAGGGGGAAGA	143279
rs564738381	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477742	TGAAGCTTCTATTCT[C/T]TTATAAACTAAAGTA	143279
rs564755935	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91474903	AATGATGAAAATAAC[C/T]GAAACCATGAGAAGA	143279
rs564756150	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433200	TCTTAACTGTTCCTA[A/T]GGGAAGAGTTATTTT	143279
rs564770203	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482453	TTGTTCTTTGTGATA[C/T]ATGAGGCTAACTCAT	143279
rs564790043	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499388	TCTTTTAGAGCTTTA[A/C]AAACTTTCTCCAAGT	143279
rs564800967	snp	C/T	0.000384468	0.0138595	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493405	AATAATAACATTATT[C/T]GTGTGTTTTTTTAGG	143279
rs564880985	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91443869	TATCCTTTATTAAAT[A/G]TGGCAACATCCAATG	143279
rs564928523	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464815	ACTCAGCCTACCCCA[G/T]CATGGACCAGTCCTC	143279
rs564939812	snp	A/T	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477197	CGTCTCAAAAAAAAA[A/T]AAAAACCCCTGCGGG	143279
rs564947352	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481585	CAATTAGAATTCTTA[C/T]GGAAAGATAAAAGGT	143279
rs564979580	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422104	ATACAGATATGATCA[C/T]GTCATATCTTGCTTA	143279
rs565001272	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492580	TTCTGTGATTTTACA[C/G]ACTTTTTGTCCATCG	143279
rs565007874	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471472	GAGTCTTAGCCAGAG[C/G]AGTTGGGCAAGAGAA	143279
rs565040282	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431169	GATATGAAATTCTGG[A/G]TTGAAAATTCTTTTC	143279
rs565142965	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91474443	GACACCTTCTAAACC[A/G]AAGGAAGTTGAAATC	143279
rs565223948	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512090	GTCTAGAGTGGTGTC[A/T]GATACAAAGTGAGGT	143279
rs565240319	snp	A/G	0.00398564	0.0444627	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437517	GGCTTATATTCAAAG[A/G]GAGGCGAATTAGACT	143279
rs565260200	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91511213	TTCTGATGCTGTGAA[A/G]TTCATAAAGACTGAA	143279
rs565273467	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91456083	TTCCATATGAACTTT[A/C]AAGTAGTTTTTTCCA	143279
rs565285075	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91463672	AATAGCAGACCTCTT[C/T]GTCTTATTCCCAATC	143279
rs565317225	snp	A/C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437976	AACAATTTATTAGAG[A/C/T]ATAATTATATTAAGC	143279
rs565353439	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449740	AAGCATTCCTATACA[C/G]AAATAATAGCCAAAT	143279
rs565367430	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412731	AAAGCTAGAATTCAG[A/C]GCTAATAGCAGTGAA	143279
rs565380550	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471514	GCACCAAAATAGGAC[A/G]AGAGGAAGTCAAATC	143279
rs565410596	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449690	AAGCAACTTCAGCAA[A/C]GTCTCAGGATACAAA	143279
rs565431121	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438450	TATTCCATGGTGCAT[A/G]TGTGCCATATTTTCT	143279
rs565468891	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91456792	TCTAAGCCTTTAGCT[C/T]ACGGACGTAGGAAAA	143279
rs565511786	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481782	AATACATTTGCATTA[C/T]TCTTTACAATTTATA	143279
rs565562023	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422475	AAATTTGTGTGTCCA[A/G]TTTGGCATTTGTTCG	143279
rs565589677	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91510378	GGCTTAAAAGATATA[C/T]ATAATTTGGTCCTGC	143279
rs565605770	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449261	ACACAAATCAATAAA[C/T]GTAATCCATTTCAAC	143279
rs565607245	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451098	ACAGCACTGTTCACA[A/G]CAGCAAAGACTGGGA	143279
rs565652100	snp	C/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91515098	TCTTAAGTAAGTATT[C/G]CTCTCCAAAACCATT	143279
rs565685585	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440233	TCATAAATAGCTCTT[A/C]TTAAGAGAAACATCC	143279
rs565696445	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91417207	AGTGGTAAAATGTTA[C/T]ACTGGTGAGCTATAT	143279
rs565751453	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431875	GAAGCCTTCTTCTCT[C/G]AACTCTTCAAAGTCA	143279
rs565785776	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476231	GATGTAGGACTCAAA[C/T]GAAGGGATTGACCTT	143279
rs565799875	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485982	CAAATTATTTAATAC[A/T]CTGCACTTTATATCC	143279
rs565845489	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91494797	GCTTGTCACTATACT[A/G]TGAGCTATTTATATG	143279
rs565863065	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431445	TTGCTAGATTGGGGA[A/C]GTTCTCCTGGATAAT	143279
rs565896195	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433913	CCATCTCAAGGCTGT[A/G]ATAAATTCTGTAAGG	143279
rs565916184	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91486699	CATAGTAAAACTAAT[A/G]TATATCTTACTGAGT	143279
rs565966676	snp	A/T	3.90701e-05	0.00441968	intron-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483109	ATTAAGAACTTTTAT[A/T]GTCTCACAGTTTTAA	143279
rs565971189	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467124	TAATGGGATTCATTC[A/G]TGACCCCCAGCAGCT	143279
rs565985676	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91466320	CTTTTGTGATTAGTC[G/T]GGCTAGAGGCTTATC	143279
rs566009877	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433347	GTTATCTCTTGTATT[C/T]TTTCCTGTGGTTTTT	143279
rs566026690	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91494147	AATGTAATTGTTTGT[A/G]GAAGAAAGGAGGGAA	143279
rs566045437	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91473943	GTTGTTCAAGGGTCA[A/G]CTGTATTTATGTGTC	143279
rs566092873	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91515293	GTTCACCCAGATGGC[C/T]GCAAATCGTTTAGTC	143279
rs566147109	snp	A/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91428610	CCCTTGTAAGTTGGA[A/T]TCCTAAGTATTTTAT	143279
rs566189161	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493005	GTGTTTTCCTTATTC[C/T]TTAGTTTTCTTTTCT	143279
rs566201975	snp	A/C	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503121	GAACAGACACTTTTC[A/C]AAAGAAGGCAACATG	143279
rs566260257	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91427735	TTGAGTTCATTGTAG[A/T]TTCTGGATATTAGCC	143279
rs566261847	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91436383	AATCAGATTCCCCAC[A/G]AAAGTGTCTTCCAGT	143279
rs566331277	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91479340	TTCTATCTGTAACAT[A/C]AATTTCAGAATCAAT	143279
rs566339429	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462579	GTAGGTCTTGGGTGA[A/T]GCCCAAGAATTTTCA	143279
rs566402350	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461851	CATCACACCCAGCCC[C/T]TAAATGTTGTTTTTA	143279
rs566418239	snp	C/T	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419561	TTATTGTAATTACTA[C/T]GTTTTTCTGCTGTTT	143279
rs566450871	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470213	TCATTTGACCAAATG[G/T]ACCTAACAGATATCT	143279
rs566509166	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422100	TAAAATACAGATATG[A/T]TCATGTCATATCTTG	143279
rs566538559	in-del	-/AG			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91414878	TAGGCAGAAAAGCTT[-/AG]ACAGTTTTTTTTTCC	143279
rs566568934	in-del	-/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457693	AACCTGCAATTAACA[-/T]TTTATGTAGTTGTGA	143279
rs566572637	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499698	GAAGTATCATAGGAT[A/G]CCTTTCAGTCACCCC	143279
rs566604235	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478689	ATATTTTTTTCTCTC[A/G]GAACTAAATATTAGA	143279
rs566640713	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91479618	AGAATGGTTGTTTAT[A/G]TGAATAATTCCACAG	143279
rs566703620	snp	A/G	0.00398564	0.0444627	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509458	ATGCCATTATTGGGT[A/G]TGTACCCAAAGGAAT	143279
rs566850486	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460990	AGTCTCCAGAAGTTT[A/C]GCTATGAAGGGAAGG	143279
rs566910014	snp	A/G	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91469325	TCCAAAGTCAAAATG[A/G]ATGAAAAAATGTTAA	143279
rs566945233	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445452	ATTAAATAAGTAATA[A/G]GTAATGAAAAAGCAG	143279
rs566956089	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91413501	ACTTTTAAAGCCATC[A/G]TTATCCAGGCCCAAA	143279
rs566993852	snp	C/T	0.0154538	0.0865337	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91507927	ACCAAAACAGAGATA[C/T]AGATCAGTGGAACAG	143279
rs567001204	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91417814	TATTGTGAATAGTGC[C/T]GCAATAAACATACGT	143279
rs567118795	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91453696	GACTTAAGTTCTACC[C/T]TATTAAAAATTACAT	143279
rs567129092	snp	A/G	0.0391387	0.134304	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91506076	TTCTTTGAAACCAAC[A/G]AGAACAAAGATACAA	143279
rs567269596	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457681	GCATCTAGAAAAAAC[C/T]TGCAATTAACATTTT	143279
rs567282041	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457075	AAATTACAGATGAAG[C/T]GGACCAATTCCTCAA	143279
rs567295089	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91413848	AGCCCTCAGAGACTT[C/T]CAGTGTTTGGGTCTT	143279
rs567317901	snp	C/T			intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91407870	ACCCTCACTGTTGCA[C/T]GTCTGACACTTGGCA	143279
rs567344693	snp	A/G	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91465191	TATCAATGTTGCTGG[A/G]AGTCAGGTTTCTCAT	143279
rs567361650	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487109	CATAACCTTTTTATA[A/C]TGTGTAATTACAAAT	143279
rs567361863	snp	A/G	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501425	CAGGATGTGTACTCC[A/G]TTTGAAGTTATTTTC	143279
rs567370577	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439468	GGTACCAGTATCATG[C/T]TGTTTTGGTTACTGT	143279
rs567373828	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483669	TAGTAGTTATATTCT[A/C]TAATGTCACCACAAA	143279
rs567388218	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91456200	TATTGATTCTTCCTA[C/T]CCATGAGCATGGAAT	143279
rs567413624	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440089	TTCTCTTGCCTGACT[G/T]CCCTGGCCAAAATTT	143279
rs567432071	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440124	TAATATGTTGAATAA[A/G]AGTAGTGAGAGAGAG	143279
rs567446891	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477846	ATTAAACTAGAATGG[G/T]AATATTATGTTAATA	143279
rs567481509	snp	A/C	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450405	ACTTAAATGTAAAAC[A/C]TAATACTGTGAAAAC	143279
rs567492211	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477674	GTATTGGCATTTGCC[C/T]CTTTCATGTAACATG	143279
rs567495201	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503585	GGGCTTAAAAAACGG[G/T]GCACCACGAGATTAT	143279
rs567521291	snp	A/G			intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91514979	ATCCAATATTTGAAA[A/G]ATCACACAGCTATTC	143279
rs567556225	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449388	TAGGTATTGATGGAG[C/T]GTTTCTCAAAATAAT	143279
rs567584474	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492671	TTGTTGATCAGTTGA[C/T]TCTCTTACTGGGAAT	143279
rs567623113	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491899	TGGAGTGTAGTGGTA[A/C]AATCAAAGCTCACTG	143279
rs567744797	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91472937	AGAAGAAATTTCTCA[G/T]AGTAGAACTCAGGGA	143279
rs567765493	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91510064	GAAGACATATAATGG[A/G]CACAATAAGCCAGTG	143279
rs567781247	snp	A/C	0.0123036	0.0774623	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91447711	AGCAAAAAAAAAAAG[A/C]AAAAAAAAGAAAAAA	143279
rs567812219	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481764	CATAGCTAGCATACT[A/G]TTAATACATTTGCAT	143279
rs567850466	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452562	ATTCATGGGTTAATG[G/T]ATTCATGGGTTATCA	143279
rs567877721	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421561	GAATTTGTGTTGGGC[C/T]GCATTCAAAGCCATC	143279
rs567908180	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91480878	GTTATAGCCTAGTTA[A/G]CTCAGTCTTTAGTTA	143279
rs567959963	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477264	CTAGGAATGATGCTG[C/G]GAAGGAGGTGTTATA	143279
rs567980694	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487908	AAAATTCGTGTTATA[C/G]TCACCCAAAAAGTGC	143279
rs567989752	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91430692	TTTTATCAGAGACTA[A/G]GATTGCAACCTCTGC	143279
rs568067866	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91443778	ACGAAACACTCTTCC[A/T]TGGTTTTAAATGAGA	143279
rs568079234	snp	A/G	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91504010	AGGCACCCTCCAGCA[A/G]GGGCACACTGACACC	143279
rs568090502	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497630	AAAATGTTTCTTTCA[A/G]TATACTTAACTTTTT	143279
rs568093648	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91443147	AGGAGTTGTGATCCT[C/T]TGGAGGGGAAGAGGC	143279
rs568192221	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91459131	TTAAAAGCTGTTCAA[C/T]CTCATTAACCATTAG	143279
rs568197384	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91424152	GATGGTTGCCACAGT[C/T]GAGGAAAAGAGAGAA	143279
rs568211386	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468616	CAAAGATCATTGAGA[C/T]TCAGGAGAAAGTAGA	143279
rs568226535	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419230	TAGTCAATTCAGAAG[C/T]GATGATGGAAAACCA	143279
rs568231012	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91418851	CTATTTTAACTTGAA[A/T]CCTATAAATATATGT	143279
rs568246395	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421710	TGCCTAGTGAGCATT[A/G]GTTCCTTTAGTAGTT	143279
rs568258246	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91423337	TAAATACATATAGGA[A/G]TGTTATAATGTATTA	143279
rs568288728	in-del	-/GA	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440131	TTGAATAAGAGTAGT[-/GA]GAGAGAGCATCCTTG	143279
rs568328546	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91459170	AAATTAAAATCACAC[A/G]GAAATATTATGCAAC	143279
rs568341878	snp	G/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91417995	CAACAGTGTAAAAGT[G/T]TTCCTATTTCTCCAC	143279
rs568343816	snp	C/T	0.00279162	0.0372561	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91427299	TATTGTGAATAGTGC[C/T]GCAGTAAACATACGT	143279
rs568389286	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458392	ATGCATTTCCTGTCA[A/G]AATTCCTGTATGTTT	143279
rs568409166	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426478	GCCAGTGCTAGACCT[A/G]TTCTACATTCTTATA	143279
rs568449968	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439895	GTTTGTCTATATTTG[A/G]TGTATAGGAATGCTT	143279
rs568489020	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450396	GGATTAAAAACTTAA[A/G]TGTAAAACCTAATAC	143279
rs568525375	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484735	GGATTTCAAAAGACT[A/G]TAGAGGCATTCTTAA	143279
rs568529403	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431548	TGGTTTGTTCACATC[A/G]TCCCATATTTCTTGG	143279
rs568595637	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420525	ACCAGGAGGCAGAGG[G/T]TGCAGTGAGCCGAGA	143279
rs568644566	snp	A/T			intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91463034	ACTTTCATATATTTA[A/T]CTTTATCTAAATACA	143279
rs568709490	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460770	TAGGCTGCAGCAAAA[C/T]AAAGGAAACACTAAG	143279
rs568720289	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91408775	TGAAATACTTTTTGC[C/T]GACTATATGGCACTT	143279
rs568776981	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91514812	AATTAAAGCCATATG[C/T]TTAAAATATTTTATA	143279
rs568783237	in-del	-/T	0.00439234	0.046657	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493411	AACATTATTCGTGTG[-/T]TTTTTTAGGCATGTT	143279
rs568815200	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91413078	GTCTAGTTTGTGTCT[A/G]TGACTCAATTCGTGA	143279
rs568887128	in-del	-/A	0.0115144	0.0749975	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493693	AGACTTAATTGAAAG[-/A]AATGAGAGTTTGATT	143279
rs568930095	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91479509	GTTTATTACTCTAGT[A/G]ATCTGTTTGCATTTT	143279
rs568971392	snp	A/G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477054	GGCGCGGTGGCGGGC[A/G/T]CCTGTAGTCCCAGCT	143279
rs568979544	snp	C/T	0.00358779	0.0422022	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490662	TTTGGGAGGCCGAGG[C/T]GGGCGGATCACGAGG	143279
rs569032563	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91511412	AAAAACCGGAATAAT[A/T]GTATCATTCATTATA	143279
rs569078677	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452823	CTAAAAGGACTGTCA[A/G]TGCAGAATCCTATAC	143279
rs569081356	snp	A/G/T			intron-variant, splice-donor-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483271	AAATCTGTTTTTAAT[A/G/T]TAAGTAACCAATTTG	143279
rs569104962	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91454724	TCGCTCCCCCCTCCC[C/T]CTACCCCACAACAGG	143279
rs569121159	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415126	CAGAAATGAAAGAGA[A/G]GAAAGATTAATAAAG	143279
rs569158231	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445890	GGTCTTTACAACCTA[C/T]AGACAAGGAGATTCT	143279
rs569165248	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461570	TTGTTTTGTTTTGAG[A/T]TGGAGTCTCACTCTG	143279
rs569213992	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422600	ATAATAAGGAATGAT[G/T]TACTTTTTCAAATAT	143279
rs569266207	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91515064	AACATTTCATTGGCC[A/G]TAGATAGATAACTTC	143279
rs569268838	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91454541	GAGGGAAATTTATAG[C/T]AGTCATGCATACGTT	143279
rs569274895	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444823	GAATATCATAATACA[C/G]TGAAAAAAGCCAAAA	143279
rs569296139	snp	A/C	0.000187869	0.00969016	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460380	TATTTTATAATTTTG[A/C]AAAGTTTAATGATTC	143279
rs569339269	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410144	GGGGTTGACGAGGGG[G/T]ACTACCGCCGGCGCT	143279
rs569365692	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502352	GCTATGACTATTAAA[C/G]ACACAGTTTAATGTT	143279
rs569394286	snp	G/T	0.00279162	0.0372561	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409620	GGGGAAGGGGAAAGG[G/T]GGGGCCCACCACGTC	143279
rs569407136	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91513915	GTTTACTATTCTCTT[G/T]GAGATGGAAGTGATT	143279
rs569453482	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91436505	AGTAATTAGTTGTTT[A/G]CTGCCACTATGTCTT	143279
rs569508033	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492958	CTGTATAATCCTTAC[C/T]ATCTGTTAAACTTTT	143279
rs569569221	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91488586	TTGAAAAAGGAATAT[A/G]GAGTAAAAAGAAATG	143279
rs569585175	snp	A/C/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464443	TGACAGTAGAAATAA[A/C/G]TATAAGGTATAAGAT	143279
rs569641321	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458239	AAACATTACAGAATA[C/T]GTATGCTTAGAATCA	143279
rs569713191	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91424329	TTCTGCTATATTATA[C/T]GAGTGAATTCTGAAA	143279
rs569792018	snp	G/T	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433212	CTATGGGAAGAGTTA[G/T]TTTTTCTTTTTTATA	143279
rs569826629	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91434740	CATTGTTCAATAGTG[A/G]GAATAACATGAGTTT	143279
rs569850986	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449878	CAAGGAAATAAGAGA[C/G]AACACAAACAAATGG	143279
rs569872462	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503617	TCCCGCACTTGGCTC[A/G]GAGGGTCCTACCCCA	143279
rs569974074	snp	C/T	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438825	GCATTTCTCTAATGA[C/T]GAGTGATGATGAGCT	143279
rs569998063	in-del	-/GTGTGTG	0.00248601	0.0351685	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415194	TCCAAATTAGAGAAA[-/GTGTGTG]TGTGTGTGTGTGTGT	143279
rs570007329	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91424929	CACAAAAATAGTATT[A/C]TTTAAATACACAGTT	143279
rs570032619	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481969	TGGAAAAGGGGGGAA[A/G]ATGACCAAGAGGTAG	143279
rs570036637	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468376	ATCAAACCCACAAAT[A/G]CATCAAAGAAGATAA	143279
rs570054377	snp	G/T	0.0023933	0.0345097	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91430790	CTGCATGTGCGATGG[G/T]TTTCCTGAATACAGT	143279
rs570136074	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91435599	CCACCTCAGGCCGCT[A/G]TGATTCCTGTTCCTT	143279
rs570153105	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501480	TGGCCTTGAAATGTA[A/G]GAGATTTTGATTAAA	143279
rs570184666	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512450	TACTGTGCCTTTAGC[C/T]TTTTCATGTTTCTGT	143279
rs570201697	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437671	TGTTGTTTTCAGATA[C/T]TTTCTTATACTGTGT	143279
rs570229425	snp	A/T	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91414945	AACAGAGGAACAACA[A/T]AATGAAATCAGTGGT	143279
rs570272695	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91465458	ACTAAAAGAACCACA[C/G]CTCCCTAGAGAAATG	143279
rs570291076	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433804	TTCGTGGTGCATGTA[A/G]TCTATACTTAGTTAA	143279
rs570355057	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470083	AAGGAACTTCTTAGA[A/G]ATCTACAAAGAGACT	143279
rs570367558	snp	A/G	1.67388e-05	0.00289294	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478172	AATTTGGTAATCCTA[A/G]TTACCTTACTGTTTT	143279
rs570388921	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497587	GTGCTGGGATTACAG[A/G]CATGAGCCACCGTGC	143279
rs570389223	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91427619	ATGATCATTTTTTCA[C/T]GTGTTTTTTGGCAGC	143279
rs570410156	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422322	TCATGACAGTTGTCA[A/G]TGAAAAAATGCCTTC	143279
rs570477641	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497750	CCAAAAACATTAGCA[C/G]ATTTTCATAGGAATA	143279
rs570478250	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91408806	ATTCTATACCTTTTG[A/T]TAATTAACAAGTAAA	143279
rs570581624	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91505955	AATCAAACTAGAACT[C/G]AGGATTAAGAATCTC	143279
rs570588628	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91416933	ATATGTCTCAGTTCA[C/T]ATTAATTTCTTTTGA	143279
rs570606277	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461772	CAGGCTGGTCTCGAA[C/T]TCCCGACCTCGGGTG	143279
rs570642388	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419492	TGTGATTATATCATC[A/C]AAAAGACCATTGAAG	143279
rs570706678	snp	A/T	0.00517822	0.0506191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91428537	TTCCATTTGTTTATA[A/T]CCTCTTTTATTTCAT	143279
rs570726131	snp	A/G	5.03267e-05	0.00501606	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512436	ATTCACTTCCCTCTT[A/G]CTGTGCCTTTAGCCT	143279
rs570734829	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410189	CGCGAGCCCCGGGCG[A/G]GCGGGGGAGGCGAGA	143279
rs570735591	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91459261	ATATTGCTGGTGGGA[A/T]TGTGAAATGGTACAG	143279
rs570775068	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91418875	TATATGTTTATTTAT[A/C]AGTCTTTTGTCATAA	143279
rs570811513	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409276	AAAAGGAGGGGGCGA[C/G]AAGAAAGGAAAGGAA	143279
rs570839281	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468261	CGGTACCAGCACCCC[A/C]CAGAGTTAGAGCATG	143279
rs570873172	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91434929	TTAAAAAGTAATTCT[A/G]TATCTTAGGAAGTTC	143279
rs570883310	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91514068	ATAAAACTGCTTCTC[C/T]CTTACACTGCTTGAA	143279
rs570914098	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476146	GTAGAGAGGGAGAAA[C/T]GGATGATACAGGAGA	143279
rs570932115	snp	A/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485844	ATACATTCATTTCTC[A/T]TTTCTTTTGTAAGAA	143279
rs570972958	snp	A/G	0.000602664	0.0173484	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425230	TTTTTGCAATAAAAT[A/G]ATTTATAGGTAGTAG	143279
rs570996695	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91413163	TATATGAATAAAATA[A/G]TATAAATATTATCAA	143279
rs571018567	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91504918	AGCCCATCAGACTAA[A/C]AGCGGATCTCTTGGC	143279
rs571032224	in-del	-/T	0.000234541	0.0108266	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484677	TTTATTATTCTATCA[-/T]TTTTTTACTTTTCTT	143279
rs571040907	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433247	AGATAACTTTTTATT[A/G]AATAGGTAACACATC	143279
rs571083744	snp	A/G			intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91463506	TAATTCTAATAGTAC[A/G]TCAGTAAATTAACTT	143279
rs571095307	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91479965	ACTTTTGCCATTTTT[C/T]ATTGCAGATTTGCCT	143279
rs571187290	snp	A/T	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451801	GGTAGGTAAAGAAGG[A/T]AGGAAGACCTTATTA	143279
rs571199004	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439766	CTTTCCTTGAGCAGT[A/G]GTTTGTAGTTCTCCT	143279
rs571257545	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91418222	TTAATTGATTGAGAA[C/T]TTTGACTGGATCAAA	143279
rs571269287	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509877	ACCAAACCCCCATGA[C/T]ATGCAGTTTACCTTA	143279
rs571269847	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91480570	AACAAAAGCTCTTGG[C/T]CAAATCTCATACTAT	143279
rs571305619	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91472640	TAAAAAGTGGGCAAA[G/T]AACATGAGCAGACAC	143279
rs571354071	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449973	GTAATTTATAGATTC[A/C]ATGCTATCCCCATCA	143279
rs571419609	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91456990	ATGATAAATGAAATA[A/G]GAGATATTACAACAG	143279
rs571554725	snp	A/C	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91455167	TCCACAATGGTTGAA[A/C]TAGTTTACAGTCCCA	143279
rs571560897	snp	A/G	0.00755907	0.0610114	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91504922	CATCAGACTAACAGC[A/G]GATCTCTTGGCAGAA	143279
rs571580314	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91511711	GAATCTAATACTGCC[A/G]CTTATGTGACAGGAG	143279
rs571594630	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501388	TTACTGCTAATACTG[C/T]TAATGATAATACATT	143279
rs571650765	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91479768	CAAAGCAGTTATGAT[A/C]ATGTATACTTCTAAC	143279
rs571655787	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91436726	TTGCCTTCCCCGTTA[C/T]ATTCCCAGTTCCTGA	143279
rs571657859	snp	C/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91446239	CCAGGCAAACAGGGT[C/G]TGGAGTGGACCTCCA	143279
rs571669862	snp	C/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445788	GCACAAGGGATCAGA[C/G]AAATCCCTCCCCTAG	143279
rs571683073	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91454596	TTTTAATACTTTAAG[C/T]TCTAGGGTACATGTG	143279
rs571700648	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91430571	GGTGCTCCTGTGTTG[A/G]GTGCATATATATTTA	143279
rs571764360	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420568	ACTCCAGCCTGGGCG[A/G]CAGAGCAAGACTATA	143279
rs571784306	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91494649	GTATATATTGTTGTG[A/T]CTAAAGGTCCAAAGT	143279
rs571795568	snp	C/T	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491752	AACATACTTTGATTG[C/T]ATTTTCATGTATTAT	143279
rs571823952	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91429591	GAGATTCAAATTCTT[C/G]CTGGTTTAGTCTTGG	143279
rs571825182	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91430736	CCATTTGCTTGGTAG[A/G]TCTTCCTCCCTCCTT	143279
rs571883736	snp	C/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437901	AAATGATATAAACTA[C/G]TGGTTTTAAACTTAT	143279
rs571894750	snp	C/T	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490759	AGCCGGGCGTGGTGG[C/T]GGGCGCCTGTAGTCC	143279
rs571938300	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91423676	AGTTAACTAATTTCT[A/G]AAAGTCTATTAATTC	143279
rs571982981	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483700	CATGGAATTAATAAA[C/T]ACAGAACCATTGCTT	143279
rs572061581	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432790	TTAGTAGAACCTTGA[C/T]ATGACATAATGAATT	143279
rs572073107	in-del	-/GGCGCG	0.00279162	0.0372561	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410284	GGGCTCGCGCGCAAA[-/GGCGCG]GGCGCGGGCGCGGGC	143279
rs572075994	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91474900	CTTAATGATGAAAAT[A/T]ACTGAAACCATGAGA	143279
rs572134470	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464822	CTACCCCAGCATGGA[A/C]CAGTCCTCTCTGAGT	143279
rs572174620	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502616	TAAATATTTACATAT[A/G]TAATTAAATTTCTAA	143279
rs572257774	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502778	AGAGTAATCTGAGCA[A/G]TCTGTTTTAATACAA	143279
rs572265369	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91475432	ATCAAAGTGTTTAAA[A/G]AAGAAGAGTATTCCA	143279
rs572283177	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415417	GTGTTTATAACAATA[A/G]TAGCTACTTATTGAG	143279
rs572294071	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500448	AAAATAGTTCCAGTT[A/T]CACTTAAAACCATCA	143279
rs572334732	snp	C/T	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91424564	TATAGTTTAATCTTG[C/T]GCTTCAAAGTATGTG	143279
rs572365872	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91414088	GGGCAGAAATAACAG[C/T]GGCAGCGAGGATGAA	143279
rs572506488	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91473433	TTACCACCAACAGAC[A/G]TATACTTAAACTTTA	143279
rs572553904	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91469586	ACCAAACCTGCCTTA[C/T]AAGAAATCCTTAAGG	143279
rs572577560	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91495115	TCACACACACAGATA[C/T]AAAACCTATAGAAAG	143279
rs572579620	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450621	AAATGTTTGCAATCT[A/G]TCCATCTGACAAAGG	143279
rs572708476	snp	G/T	0.00199481	0.0315187	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410258	GGGGCTGGCGCGCGC[G/T]GGGGCGGCCTCGGGC	143279
rs572713104	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91456823	GAAGAGAAAATCAAC[A/C]GAAAGCAAGCAGGAA	143279
rs572767568	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419002	GAATTTTATAGACAT[A/T]GACGTTCAATTTAAA	143279
rs572917486	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476916	CCGGGCGCGGTGGCT[C/T]ATGCCTGTAATCCCA	143279
rs572959079	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415932	AAAAGGGAGGGCTAT[A/G]GCTTTATAAATACAT	143279
rs573001855	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445123	CACTGTTTTCACAGA[C/T]GTCACAACTCTCGTT	143279
rs573019669	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91413056	CCCCAGCCTAATGGT[C/T]CTGCCTGTCTAGTTT	143279
rs573021234	in-del	-/A	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421512	AAAAGAAAAAATCAC[-/A]AAAAAAAATTTATAA	143279
rs573066825	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91454032	AGTTGTAAAAACTGC[A/G]GGAGAAAAACTGGTA	143279
rs573071988	snp	A/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91436040	TTTTATAGTACCCTT[A/T]TATTTCATGGTTATA	143279
rs573085657	snp	A/G	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91506680	ATGGATTCACAGCCG[A/G]GTTCTACCAGAGGTA	143279
rs573105404	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91434660	TATAGTTTAATGGCT[C/T]CTACACCCATGTGAA	143279
rs573118059	in-del	-/AAG			intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91408149	GGACATTTATTTAAT[-/AAG]AAGTCAAAGGAAACA	143279
rs573170611	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91443459	CCTCTGGAAGCTTTG[A/T]CCCAGAGGGGCACCT	143279
rs573177649	snp	A/G	0.0023933	0.0345097	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457961	AAGAAGAAAAAAGAC[A/G]TACAGATTAGAAAAT	143279
rs573222479	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91466809	TATCATGGAAATTAT[C/T]CAGTGATAAGAAGAA	143279
rs573226427	snp	A/G	0.00438332	0.0466095	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91504336	ATTACTCTGAGCTAC[A/G]GGAGGACATTCAAAC	143279
rs573288076	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91515312	AATCGTTTAGTCTAG[G/T]GCCTAGGTTTTGGAG	143279
rs573316621	snp	A/G	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91434687	TGAATTTAGTTTTCC[A/G]TTTTATTATTTGTTT	143279
rs573347615	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91459385	ATAACCTCTACACAA[A/G]TGTTTCTAGCAGCTT	143279
rs573424124	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487024	CATTCTTTCTAAATG[C/T]ATTTATCTCTGTGTA	143279
rs573424552	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91443999	GGTAATCTTTATGAA[A/C]GGGAAAGAAAAGGGC	143279
rs573453389	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91480820	GATGATTTTATTACA[C/T]ACCTAACTACTTCCA	143279
rs573458184	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422774	TCTTTTCAATTTTCT[C/G]TCTTATCTTTGAGAC	143279
rs573518908	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431525	GGTACACCAATCAGA[C/T]GCAGATTTGGTTTGT	143279
rs573520766	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422059	TTTATTCTATTCCCT[A/G]GACTGCTACCATAGT	143279
rs573550114	snp	A/C	0.00478085	0.0486577	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438302	GTGTTCTCATTGTTC[A/C]ACTGCCACTTACGAG	143279
rs573554538	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497821	ATGTGGCAGATAGCA[A/G]TGAATTATGACAGAC	143279
rs573563594	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449551	TTGGCCAGGGCAATC[A/C]GGCAAGTGAGAGAAA	143279
rs573592393	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91504982	AATATTCAACATTCT[G/T]AAAGAATTTTCAACC	143279
rs573649730	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449169	CAGCGCATCAAAAAG[C/T]TCATCTACCACGTGA	143279
rs573734613	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468768	TTACCCCATCTCTAC[A/C]AAAAAAAATTTTTTT	143279
rs573737157	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490808	AGGCAGGAGAATGGC[A/G]TGAACCCAAGAGGCG	143279
rs573749184	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91448907	ACCAACCAAAAAAAG[C/G]CCAGGACCAGACAGA	143279
rs573775343	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91489695	CTATGCTAGGAATGC[A/G]GACTTCCTTGATAAG	143279
rs573809828	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91480136	GACTGAAGGGTTAAG[A/G]CCAAACTGGGAGTTA	143279
rs573813948	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499911	TAATATGTTTGTTGT[C/T]GAAAATACCTTTGAA	143279
rs573857465	in-del	-/AGAC	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452065	AATCAATGAACTGGA[-/AGAC]AGAACAATAGAAATT	143279
rs573895319	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502401	AAAAGTCATTATGTA[C/T]TGAGTTTCTCAAATA	143279
rs573911930	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438999	GTCAGATGGATAGAT[C/T]GCAAACATTTTCTCC	143279
rs573915045	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482337	GTGCTAGAATTTTAT[A/G]TTTTGGAAACATTAA	143279
rs573934680	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91472998	TGTATAGAGGTTAGA[A/G]TAAGAAAGACTAAAC	143279
rs573935664	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419823	CCCCAGCCCACTGTT[G/T]GTAGGCTGGCCACAT	143279
rs573955647	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415717	CAAAGAAGCTGCACC[C/T]ATGGCAGTATTTCTA	143279
rs573962723	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493112	CATAATTTATAATCT[A/G]TGAAACTATACTTTT	143279
rs573979014	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481294	GAAGATTTTTTTTAA[A/G]GTAGGATTAATAAGA	143279
rs573990347	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412637	TTATTTTTTAAAAAA[A/T]AAAACAATTTATGAC	143279
rs573998149	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470299	CACATACTTTAAGAT[C/T]GACCACATAATCATA	143279
rs574013327	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478590	CTGAAATAATGAGCA[C/T]TAAATTTAGCCTTGG	143279
rs574075325	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91430004	CTTTCCTGCTTTCTC[C/T]TGTGGGCATTTAGTG	143279
rs574081574	in-del	-/TTAA			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91495053	TTTCAAGTTAAACAA[-/TTAA]ATCTAAAAATTATAA	143279
rs574097229	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91441897	CTTGCTTTTTTTTTT[C/T]TTTTTTTTTTCTTTT	143279
rs574171291	snp	A/T	0.00279162	0.0372561	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412621	CAGTACCATTGATTA[A/T]TTATTTTTTAAAAAA	143279
rs574272350	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464690	TTGGTACTGGATGCC[A/G]TCATAACATGCTGAC	143279
rs574272439	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91455896	GTAGATGTGTGGTAT[A/T]ATTTCTGAGGGCTCT	143279
rs574274826	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91479783	AATGTATACTTCTAA[C/T]AGCAGAGGGCCTGAG	143279
rs574333722	snp	A/G	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91463331	AAGTGGAAGTGGACT[A/G]TCATAAAGGTCTTCA	143279
rs574416273	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420706	AAAGGAACAGAGACT[A/G]GCTGTTTTTTGTGCC	143279
rs574440355	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91416539	CTATATCATATAACC[C/T]AGGTGTGTAGTAAGC	143279
rs574474264	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457905	GCTCTTACTCTTATT[C/T]ATCTCAGTGCTGCAA	143279
rs574505730	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91424598	AGATTTTTTGTATAA[C/T]TACAAAATACTGATT	143279
rs574537696	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457319	TTACAAAGCTGGTAT[C/T]ACACTGATAACAAAA	143279
rs574577044	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91486243	CATTTCACATCTGAA[C/T]ACTCAGAACTGAATA	143279
rs574599156	snp	A/G	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91489417	TGGTACAATCTAAAT[A/G]TACAAAATTGGTTTC	143279
rs574632591	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467885	TAGCAACTAGCCCCC[C/T]CACCATGCTGACACC	143279
rs574655491	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91408933	ACTTGTTACAAATTG[C/T]GGGTTTGAAAACATG	143279
rs574666940	snp	C/T	1.7038e-05	0.00291868	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460390	TTTTGAAAAGTTTAA[C/T]GATTCATTATTTTGA	143279
rs574668826	snp	G/T	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452298	CTAAACAAACCTCAT[G/T]CAGAAGAAATCCAAA	143279
rs574731990	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91459458	TAGTTAACCATATAG[C/T]GGTACACCCAAATAG	143279
rs574734527	in-del	-/ATTT	0.0023933	0.0345097	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491833	TGATTCCGCTATGTG[-/ATTT]ATTTATTTATTTATT	143279
rs574735673	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467374	TCAAGGCTCACTGTG[C/T]TCCTCCTGGAGACTT	143279
rs574795871	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91465864	GATTTTTTTGCATCT[A/G]TGTTCATGAGAGGTA	143279
rs574820014	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91466575	CACTGCTTTTGCTAT[A/G]TCTCACAAATTTTGA	143279
rs574878076	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91414203	TACATTGGGTTCAAG[A/G]AAGAGCTAGATTTGA	143279
rs574943957	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497811	ATAAACAGTAATGTG[A/G]CAGATAGCAGTGAAT	143279
rs574945553	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439724	CATGAGGATGGAATG[A/T]TTTTCCCTTTGTTTG	143279
rs574973554	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91411411	AATATTTAAGTACTT[C/T]TTGAAAGTTTGCTTT	143279
rs575026851	snp	C/G	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503394	CTAGGGAGTGCCAGA[C/G]AGTGGGCGCAGGTCA	143279
rs575063589	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91514108	CAGCTTTTTAATGTA[A/G]GTTACCACTTATAAG	143279
rs575141611	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458082	AGAATTAATAAGTGA[A/G]TTCAGTATGGTTGAA	143279
rs575196506	snp	A/G	0.00014925	0.00863729	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462058	AGAATAGTCTTTAAA[A/G]TGTTGAATATACTTA	143279
rs575229554	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91455149	GGAATCGCCACACTG[A/T]CTTCCACAATGGTTG	143279
rs575304338	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500799	ATGAAATCACTCCCT[C/T]TGGGAGAAAATTCTA	143279
rs575337494	snp	C/G/T	0.375	0.216506	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410599	GTGGGCCGGGGCCGT[C/G/T]TGGCGCCCCGGACGG	143279
rs575339899	snp	C/T			intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481476	CTCCTCCATTCAAAC[C/T]TGTTTCTTGTAACTA	143279
rs575343116	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437522	ATATTCAAAGGGAGG[C/T]GAATTAGACTCCATC	143279
rs575455540	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91418601	GACTTTTCATATCTT[A/C]GTAGAAGGATGTAGA	143279
rs575455604	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91427791	AATTTTCTCCCATTT[A/T]GTAGGTTGCGAAAAA	143279
rs575480053	snp	A/G	0.00676609	0.0577691	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431847	CCTGTAGCTCGGAGT[A/G]GTTTGATTGTCTGAA	143279
rs575571220	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91411657	TCTGAGGGCCCTGAT[A/G]ACTGGAAATTGTTAA	143279
rs575604172	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91510170	AAAATAATCTTCAGT[C/T]ATTAATTGTATTCAG	143279
rs575605738	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444110	CCTATAGAGTTTTTC[C/T]TCCTCTTTACCAGGC	143279
rs575622839	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91443575	AGGGACCCACTTGAG[C/G]AGGCAGTCTGTCCCT	143279
rs575642779	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509291	AAAAAAAATAAATTT[A/T]AAAAAAAAATCAAAA	143279
rs575680400	snp	A/G	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91504471	AGGCTCGAGAACCAC[A/G]TGAAGAATGCAGAAG	143279
rs575689214	snp	C/T	0.0232847	0.105357	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91505008	CAACCCAGAATTTCA[C/T]ATCCAGCCAAACTAA	143279
rs575717622	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420025	TCTCTAATATTAATC[A/C]TTTTGCCATTGCACA	143279
rs575767893	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512826	TAGCCATATTTTCAT[A/G]TAGTGGTATACAACA	143279
rs575829127	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91454831	GGTGTTTGGTTTTTT[G/T]TCCTTGCGATAGTTT	143279
rs575846643	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451918	ATATATGTATATTTC[A/T]TTATTATAGACCTTA	143279
rs575856255	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91414557	ATGAAAAGCAAAGCA[A/G]TATGTAAAAACCACA	143279
rs575891851	in-del	-/ATT	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444753	AGACCTCAAACTGAC[-/ATT]ATAAATAGAGGCAAA	143279
rs575907748	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493323	TTATTGTTGAATTGA[C/T]TAGCTTCTAATAGAT	143279
rs575936015	snp	A/C	0.0115144	0.0749975	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431612	CTAAACTTCCCTTCT[A/C]ACTTCATTTCATTCA	143279
rs575991318	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91488349	TAGGCAAATTGTAGA[A/G]CAGTATGAAGTTATC	143279
rs576007298	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91424992	AATGTGCAAGGAACA[A/G]TGCTAATTATGTGCA	143279
rs576018066	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484802	TTATTTTCTACTTTG[A/G]TAATAGATTTCATAA	143279
rs576041404	snp	A/G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461121	ATAAATCCATAAACT[A/G/T]TATTAACTGGGACAT	143279
rs576058695	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91480920	AGCCTAGGAGAGGCA[C/T]AGAAGCACTTGTATT	143279
rs576071522	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91459386	TAACCTCTACACAAA[C/T]GTTTCTAGCAGCTTT	143279
rs576109547	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439158	TCTGTGCCCACGCCT[A/G]TGTCCTGAATGGTAT	143279
rs576121483	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502134	TTTAGATCATATTTC[C/T]GTGGGAAATAACTTT	143279
rs576133482	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91510295	TTGCAAAGCAAATTT[C/T]AAATTACATCCTTTT	143279
rs576171077	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450134	ACTTCAAACTACAAG[C/G]CTACAGTAACCAGAA	143279
rs576205361	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512033	AATGAGTTTCATGAA[A/G]GTGGTAACATTGGTT	143279
rs576322547	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432080	GCATGGAGTTTATTT[G/T]TTAAGGGCACTGCAG	143279
rs576457729	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476860	CCTAGCAAAGAGGCT[A/G]CTCAGGATGGGGAGG	143279
rs576465857	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421606	CCCTGGGGGCTGTGG[A/G]TTGGACAAGCTCGTT	143279
rs576480684	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490869	GCAGTCCAGCTTGGG[C/T]GAAAGAGTGAGACTC	143279
rs576496941	snp	C/G	0.00358779	0.0422022	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91430299	GAGCTTTACTTCCAA[C/G]TATGTGGTCAATTTT	143279
rs576528627	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420952	TGGGGACCATGAGTG[C/G]GGCAATTTAAATATA	143279
rs576558470	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457101	CTCAAAAAACAAAAG[C/G]TATTGCAGCTCATCC	143279
rs576581703	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91505261	TGACAGGATCAAATT[C/G]ACACATAACACTATT	143279
rs576604240	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503567	ATACTGCGCTTTTCC[A/G]ACGGGCTTAAAAAAC	143279
rs576686671	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449664	TCAGCCAGAAATCTC[A/C]TTAAGCTGATAAGCA	143279
rs576687910	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431900	AAGTCATTCTCCGTC[C/T]AGCTTTGTTCCATTA	143279
rs576802131	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451303	ACATGTTCTCACTCA[C/T]AAGTGGGAGTTGAAC	143279
rs576847123	snp	A/C	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91413414	TTGGTAGCATATTAA[A/C]GTCCTCATTCCTACA	143279
rs576859910	in-del	-/AC	0.00199481	0.0315187	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512839	ATATAGTGGTATACA[-/AC]ACAGTATCATTGCAA	143279
rs576870793	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409114	AATTCACTCAACCTC[C/T]AATAAAATAATGAAG	143279
rs576871442	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91489473	ACAGTGTCAAGAATT[A/G]TATCATTGTTGGGTT	143279
rs576894426	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91486205	ATTGGCCTGAAACAT[A/G]GAATGGGCTTCTGGA	143279
rs576902915	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91407834	CTAGTTTTTCCAAAG[C/T]GAATGAGTTTATACT	143279
rs577006117	snp	A/G	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91453154	AAGAAAATTATGGCC[A/G]AGTGCAGTGACTCAC	143279
rs577025324	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91443304	GATGTTGATGCTATT[C/G]CTTTCTGTTTGTTAG	143279
rs577144104	snp	A/C/T	0.0119091	0.0762411	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464787	GCCCCATGACACAGC[A/C/T]CACCTCACAGCCACT	143279
rs577144375	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426541	TTTACCTTTGATAAC[G/T]TCTTTCTTTTATTTG	143279
rs577204113	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485383	TTTAAGTTTATATGA[A/G]GTTTACACATACGTT	143279
rs577259268	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409663	ACCTCCAGGCTTTTC[C/T]TGTGTAGGCTGAAGC	143279
rs577260488	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445894	TTTACAACCTACAGA[A/C]AAGGAGATTCTCTTG	143279
rs577276147	snp	C/T	0.00795532	0.062565	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438470	CCATATTTTCTTTAT[C/T]CAGTCCATCATTGAT	143279
rs577320704	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91514436	TTTTTGGTTTACAGT[G/T]TAATAATACCTCATT	143279
rs577331275	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485536	GCATCTTTTCAAGAA[C/G]GGAGAGGTTCTATCT	143279
rs577355341	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91424752	CTTCTAAAAAAAAAT[C/T]CTGGTATGCCCAATC	143279
rs577355882	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433580	AACTGGATTTATTTA[C/G]TCAGATTCCTATTAA	143279
rs577366074	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412455	ATACAAAACTTGAGG[A/G]TTTTTTTTTTTTCTT	143279
rs577369137	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432896	GGTCTTCAGCTGAAA[A/T]CGCAATTGGATCTGT	143279
rs577406980	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91430835	TGACTCTTTATCCAG[C/T]TTGCCAGTCTGTGTG	143279
rs577421189	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438214	ATTAAGTATTTCTCC[G/T]AATGCTATCCCTTCC	143279
rs577467293	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91495742	ATGTTTATATCCATA[C/T]GTTTATTCAGTTTAG	143279
rs577482319	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437655	GTTGTTTTGTTTTTT[A/T]TGTTGTTTTCAGATA	143279
rs577514143	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91488579	TTCTTAATTGAAAAA[A/G]GAATATAGAGTAAAA	143279
rs577546019	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449139	CTCAGTAAAATACTG[C/G]CAAACCAAATGTAGC	143279
rs577604372	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91455600	CATTTGTCAATTTTG[G/T]CTTTTGTTGCCATTG	143279
rs577611499	snp	C/T	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91504124	CACCAAAAACCCATC[C/T]GTACATCACCATCAT	143279
rs577615850	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91469267	CAGAGAACCCCTGCA[A/G]TATGCAAGATGACCA	143279
rs577646188	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503696	GCGGCAGCGAGGCTG[A/G]GGGAGGGGCGCCCAC	143279
rs577664577	snp	A/G	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91510664	GCATAAAAATAAGTT[A/G]TGTAGCTTAGGACCT	143279
rs577682549	snp	C/T	1.64844e-05	0.00287087	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462172	TGCTGTGTATGATAC[C/T]TTACTTAATACTGTA	143279
rs577751682	snp	C/T	0.0123036	0.0774623	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91506371	ACAAAATTGATAGAC[C/T]GCTAGCAAGACTAAT	143279
rs577759541	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421022	GATCTTCCCTCAAAC[A/C]TTTGCATTCTTCCCC	143279
rs577764280	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91473257	GAAAATTATTTGGCT[C/G]TCAGCAGACTGCTCC	143279
rs577775479	in-del	-/AGTA	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470781	CTCTGAAATTGAATC[-/AGTA]AGAAACAGCTTACCA	143279
rs577786648	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512700	GAAAGCAAAGTACAG[C/T]GAAGAATGAATTTAT	143279
rs577798675	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91469565	ATGCTAAGGAAATTC[A/G]TTACCACCAAACCTG	143279
rs577798951	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492102	ATTAAAAATTTGAAG[G/T]CAGTAGATACCAGGA	143279
rs577805881	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91480063	CTCACGTTTCAGAAA[A/G]TCAGTTACTAGACTC	143279
rs577836897	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449515	TCTCTTACTACTCCT[A/G]TAAACATATTATTGG	143279
rs577844762	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490975	TACAGAAGGTGAATT[A/C]TTTTTGGTCCTCCAC	143279
rs577869345	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91466100	TAACAGTTATTGATT[C/T]GGTTCCTTTAGTAGA	143279
rs577875629	snp	A/G	0.00517822	0.0506191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503327	CCCAGCCTGAGCGAC[A/G]CAGAAGATGGGTGAT	143279
rs577932052	snp	A/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91488524	TGCTTGTGTTACATG[A/T]TTGCTCACAATTTTA	143279
rs577959037	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91427826	TCCCATTTTGTAGGT[C/T]GCCTGTTCACTCTGA	143279
rs577981249	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501762	TATTACCAGAAGTAC[C/G]TCTAATACTAATCCT	143279
rs577987175	snp	A/G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440446	TTGATTGTGGTGGAT[A/G/T]AGCTTTTTGATGTGC	143279
rs578008979	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500962	GCAGGAGAAAAATGG[C/T]TCCTGTACTATCCAC	143279
rs578032657	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476680	CTTGCCCTATCCTGT[G/T]GCTGGCTTCTTTCTC	143279
rs578047592	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439419	TCTGAGACCTTTATC[C/T]GGTTCCATTGGTCTA	143279
rs578048897	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499268	AAATATTTTCTACTT[G/T]TTAAAAGTAGAACTA	143279
rs578057595	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91474193	ATAACTTTCTTAACT[A/G]GAGAGTAGGGGAATG	143279
rs578063841	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498296	GATTAACCAATACAT[A/G]CAATCCTCTGTCTTA	143279
rs578118302	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91435123	AAAATTAAAACCCAA[G/T]AACTCAGCAATCAAG	143279
rs578120580	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419733	AATTCTTAGTGTTTT[C/T]CCCTGTGTTCTCTAT	143279
rs578178924	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478516	TGTATGTAAAGTTTT[C/T]TCTATGCAGATATAT	143279
rs578204815	snp	A/C	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91489561	ACTAATCTTGTTTGC[A/C]ATTAGCATCCTAGCA	143279
rs578207817	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91429022	TGTGGGTTTGTCATA[A/G]ATAGCTCTTATTATT	143279
rs578231208	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470635	ACCTAGAAAATCTAC[A/G]GAAACAAGCACAAAC	143279
rs578250415	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477871	TTAATAAACATGTTA[C/T]GCTTGGATTCTTGTT	143279
rs745324269	snp	A/G	1.65138e-05	0.00287343	synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460443	GAGAGAACCACCACC[A/G]ATTTGCCTTGATGTT	143279
rs745378141	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461747	AGAAACAGGGTTTCA[C/T]CATGTTGGCCAGGCT	143279
rs745431787	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451689	TAGCATGTTTATACT[A/C]TCTTCTAATATGGAA	143279
rs745456278	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91488016	GTAGGAAGAGTAAAT[G/T]CTTCTCACAGATTCA	143279
rs745475531	snp	C/G	1.65446e-05	0.00287612	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484599	CTGAAGAATTTCCAC[C/G]TATAACAAAGTGTTC	143279
rs745516046	snp	C/T	1.8244e-05	0.00302021	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425383	AGAAGTTCACCTGCA[C/T]ATCTTGTTTTCCCTA	143279
rs745538798	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91513336	TTTTTGATCACCAGT[C/T]GTACCAAAACACTAA	143279
rs745569948	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485935	CCACAGCTTATTTAT[A/T]ATAATAATTAATAGA	143279
rs745613587	in-del	-/T			intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481637	GCGAAGATAATGAAC[-/T]TTTTCCTCTTGATAG	143279
rs745653301	in-del	-/C	1.81145e-05	0.00300947	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483087	AAAAAGTAAATCATT[-/C]TATGATATTAAGAAC	143279
rs745654412	snp	C/T	1.65192e-05	0.00287391	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496248	ATAACAGCATCACCT[C/T]GGATATTCGTTTCCC	143279
rs745662262	snp	C/T	1.68247e-05	0.00290035	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478160	TAAACGTCACCTAAT[C/T]TGGTAATCCTAATTA	143279
rs745701338	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478641	AAATTTTTCTTATTT[A/C]TATTATAGGGACGCC	143279
rs745741988	in-del	-/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458264	GAATCATACCATGCT[-/G]GTGAAAGAAATTAAG	143279
rs745744284	snp	A/G	6.8341e-05	0.00584516	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493495	ACTATTCTGAATTCC[A/G]ATTGGTTGGAATTGT	143279
rs745765665	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412768	AAGTGTAGAAAATCT[A/G]TGCTTGGTCCTTAGT	143279
rs745776479	in-del	-/AC			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470976	CTGTGTGGCAGAGAC[-/AC]ACACACACACACGCA	143279
rs745888263	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492829	ACTATAGTTTGCTCT[A/G]TAGTAACATTTAAAG	143279
rs745902290	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91456575	CCCTTTATTTCTTTC[A/T]CCTGCCTGATTGCCC	143279
rs745935073	snp	C/T	1.64928e-05	0.00287161	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501251	GAAGTTGCTACATTT[C/T]ACTACAGGGAGTGAC	143279
rs745962657	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420352	GCACTTTGGGAGGCC[A/G]AGGCAGGTAGATCAT	143279
rs746002621	snp	C/T	1.85276e-05	0.00304359	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487625	CTTAGATTCCCTTAG[C/T]ATAATTTTGTTAAAA	143279
rs746002643	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490223	ACAATTTTATTTCCT[A/G]CTTTCTTCAGTGTAC	143279
rs746092499	snp	G/T	5.08066e-05	0.00503991	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410487	ACTCCGCTGGTGGTG[G/T]CGGCGCCCGCGCCTG	143279
rs746117086	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451183	GCACCATGTAATACT[A/G]TGCAGCCATAAAGAA	143279
rs746132909	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91466976	GGAGGAACATCTGCC[A/G]CGGAGAGACTGGACA	143279
rs746207635	in-del	-/T	5.1856e-05	0.00509169	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496179	ATTTGTTGTCATGGA[-/T]TTTTATGTTAATGCT	143279
rs746212961	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458397	TTTCCTGTCAAAATT[C/G]CTGTATGTTTTTTGT	143279
rs746258389	snp	C/G			intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91407882	GCACGTCTGACACTT[C/G]GCATAGCTAAAAAGC	143279
rs746297426	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432295	ATTCTCTAACAGCTT[C/G]TTTGCCCGTCTGATC	143279
rs746355935	snp	A/G	1.65078e-05	0.00287291	stop-gained, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461289	AGTCATCAGGAGATT[A/G]GAAAGCAGTACATGA	143279
rs746383751	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467184	GGAGCAGCCTGCTCT[G/T]GCCACGGGCCTCCGG	143279
rs746416336	in-del	-/AGA			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412354	TACTACTAGACAAAG[-/AGA]AGAATATATTCAAGA	143279
rs746434702	snp	A/T	1.6741e-05	0.00289314	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460606	TGTATAGTCATCTGC[A/T]TGTCAGCACTTTACA	143279
rs746436628	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91459351	TTTACCTCAAAGAAA[A/T]GAGGAATTATTTTAC	143279
rs746539671	snp	A/G	1.65037e-05	0.00287256	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496257	TCACCTTGGATATTC[A/G]TTTCCCTCCCTGCTG	143279
rs746554390	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444600	AGAAAAGAAAAATAA[C/T]AGACTGCAGCTGTTC	143279
rs746569149	snp	C/T			intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481505	TAGTTTTAACAGGCT[C/T]CAGGATTTTCTTTTA	143279
rs746582560	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91511658	GCAACCTAGATTCCT[C/T]GCACGTGCAGTTCAC	143279
rs746661160	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477691	TTTCATGTAACATGA[C/T]ACAAATTTTACTGAT	143279
rs746690777	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91510090	CAGTGCAGGATTTCA[A/G]TTTTAAATTCATAGA	143279
rs746693352	in-del	-/TAAAAAA	1.65258e-05	0.00287448	frameshift-variant, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512297	TGCTTCAATCAACTT[-/TAAAAAA]TGCCTTCCCCCCTAC	143279
rs746710175	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91443643	CTCTCTTCACAGCTG[C/G]CAGGCAGGAATGCTT	143279
rs746716912	snp	C/T	3.29843e-05	0.00406092	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460471	GTTAGACAAAAACAG[C/T]GTACATCTATGGATG	143279
rs746746739	snp	A/G/T	0.000124173	0.0078787	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410490	CCGCTGGTGGTGGCG[A/G/T]CGCCCGCGCCTGAGG	143279
rs746839829	snp	A/G	1.65583e-05	0.00287731	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501311	GAACTTTAAAATCTC[A/G]AAGAATGAAACTTCT	143279
rs746850709	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91473354	ATTGATTGATGTAGC[C/T]GGAGAAACTGACTTT	143279
rs746905133	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91434134	TCTGATGGCTAAAGT[A/C]CTGTGAGTCAGACTT	143279
rs746907231	snp	A/G			upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91408749	CATTTTCCCTCCAAG[A/G]CTATTAGCACTGAAA	143279
rs746914964	snp	A/G	1.73195e-05	0.00294269	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496398	AGTTATTAATATCTT[A/G]TCCTTTAATGCGAAA	143279
rs746945191	snp	C/G	1.95429e-05	0.00312587	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482924	TCTTTCCTTTTACGT[C/G]TTAACAGAATTTTAA	143279
rs746955764	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458401	CTGTCAAAATTCCTG[C/T]ATGTTTTTTGTTGTT	143279
rs746964987	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451938	TATAGACCTTAAAAT[C/G]TATAAGATATTAATC	143279
rs746977665	in-del	-/CTC			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91473617	AGACAGGAAGACCAA[-/CTC]CTCCTCTTCAGCCTC	143279
rs746993986	snp	A/C	1.71182e-05	0.00292554	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478300	ATTTAGCTAATCAGT[A/C]TAGATGTCTAACTTA	143279
rs746996761	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432784	ATGAGTTTAGTAGAA[C/T]CTTGATATGACATAA	143279
rs747057513	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502182	TAGAATCCAGAGACT[A/G]TAAAATAAAGCTCTA	143279
rs747062799	snp	A/G	6.60382e-05	0.00574585	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461301	ATTGGAAAGCAGTAC[A/G]TGATTTTTATCTAAC	143279
rs747063198	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439131	ATTGCTTTTGATGTT[G/T]TAGTCATCAAGTCTG	143279
rs747086860	snp	C/T	1.66527e-05	0.00288549	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491292	GACACATCTGGTTAG[C/T]GATTCACTTGATGAG	143279
rs747111142	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91514258	ATGTGCTTGTATATC[A/G]ATTAGCTGTGTCACT	143279
rs747147243	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500310	CTATTTACAAGATCT[A/G]TAAACTTCGGAAGCA	143279
rs747174730	snp	A/G	1.65364e-05	0.0028754	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512290	CCCATACCTGCTTCA[A/G]TCAACTTTGCCTTCC	143279
rs747176683	snp	G/T	3.34409e-05	0.00408893	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487653	AAAATACACCATTTT[G/T]CTTTTTCTTTTTTTC	143279
rs747193633	in-del	-/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91511428	GTATCATTCATTATA[-/T]TATCTACTCCTCGGC	143279
rs747243687	in-del	-/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432201	TTGCCAATAAGATTG[-/T]TTTTTTCAAAGATGC	143279
rs747293955	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91466312	CTCACTTCCTTTTGT[C/G]ATTAGTCTGGCTAGA	143279
rs747322962	snp	C/T	1.80693e-05	0.00300571	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498866	TGTAATGGCATCTCC[C/T]ATCAGGTTTTTCAAG	143279
rs747372721	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470227	GGACCTAACAGATAT[A/C]TGCAGAACTCTCCAC	143279
rs747373921	snp	A/T	1.68581e-05	0.00290324	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484395	TTAAGAAATAGAATT[A/T]GGGGGAATAGTCTAA	143279
rs747388627	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426255	GTTTTATCACGGGAA[A/G]TGTACATTACTTAAA	143279
rs747438901	snp	C/G	3.29881e-05	0.00406115	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499083	TCCTTCTGAACAAAT[C/G]CATCTATAAGCAGTT	143279
rs747463483	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458267	TCATACCATGCTGGT[G/T]AAAGAAATTAAGATC	143279
rs747551111	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457190	CTTTAAAAAAGGAAT[A/G]TTCACGTCCGGATGG	143279
rs747619116	in-del	-/T	0.00439234	0.046657	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493410	AACATTATTCGTGTG[-/T]TTTTTTTAGGCATGT	143279
rs747654114	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492302	TTAAAAATGTTAATT[A/C]TCTTTTCACTGCTCT	143279
rs747656116	snp	C/G	3.35841e-05	0.00409767	missense, intron-variant, nc-transcript-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482984	TCCTCAGTTTAATAA[C/G]ACATCTACGTATGTC	143279
rs747724786	snp	C/G			upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409909	GCCAGGGCCGTCCGT[C/G]AAGGGTAGTCTGTGC	143279
rs747738672	snp	A/G	1.64876e-05	0.00287116	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496288	TTACAAGAAATTATT[A/G]AGCCCTCCCATCATT	143279
rs747747402	in-del	-/TAAG			utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512504	CCAACTTTAAAATAT[-/TAAG]TAAGTTTTTAAAAAA	143279
rs747774144	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419397	TTTAACTATATGTTA[A/G]TAGCAGAACAGGTAC	143279
rs747850033	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91473103	ATAACTGATGTAAGA[C/T]GTGAATCCACAAATA	143279
rs747893706	in-del	-/AATCATTTTGTATAT	0.000102722	0.00716593	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487547	AAATTATACACATAC[-/AATCATTTTGTATAT]GGTAAAACACAATCC	143279
rs747901824	snp	C/T			intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91408010	TGGCAGTTGGGAATG[C/T]GTCTCTCAAGCACAC	143279
rs747915999	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509444	CATTCAACCCAGCAA[C/T]GCCATTATTGGGTAT	143279
rs747935488	snp	G/T			intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91463642	ACCTCTTTCACAATT[G/T]TGAATAAAAGAAGTA	143279
rs747941027	in-del	-/A			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415869	CATTAAATTATATGT[-/A]AAAATCAATCTGATT	143279
rs747951043	snp	G/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91513751	ATGCAAATAATACTT[G/T]CCCCAAAATCTTTCT	143279
rs747957594	snp	C/T	1.65356e-05	0.00287533	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512372	AAATTCAGAAGGTTT[C/T]GGACTTGAGTAACCT	143279
rs747970976	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91417055	TAGTTAAAGTTGAAG[A/G]AGAGTAGAGAAAGAT	143279
rs748029061	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91456127	AGCCATTGGTAGCCT[C/G]ATGGGGGGGTGGCAT	143279
rs748040618	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490019	ATGACATATTCCTTA[C/T]AGATATTTTTAAATA	143279
rs748082460	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91489873	TATTAAAGCAAATTG[C/T]TGCATGTATTTAAAA	143279
rs748108634	snp	C/T	0.0555102	0.157079	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410603	GCCGGGGCCGTCTGG[C/T]GCCCCGGACGGCGGG	143279
rs748144200	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431987	AGACCTTTTAGCAGA[A/C]TTCCTTTATCTTATT	143279
rs748144559	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498456	AGCTTTTTAGTTTCT[A/G]AAAATAAGCCTCTCC	143279
rs748172519	snp	C/T	1.65493e-05	0.00287652	intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462221	TAATATTATTCTGTG[C/T]CTCTTCTGTATATCA	143279
rs748204137	in-del	-/AAAA			utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91513974	AGGGTATTTCTTCTT[-/AAAA]AAAAATCTTGGAAAG	143279
rs748331581	in-del	-/ATTAA			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91413961	GCTGATGATGTGAAT[-/ATTAA]ATTTACTGAGGTTGA	143279
rs748333373	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478319	ATGTCTAACTTACAC[A/T]TCATATATCTTTAAC	143279
rs748365360	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438100	GCCATCTTTTTTTTT[G/T]TCTTTAAGTTCTGGG	143279
rs748368860	snp	A/G	1.64857e-05	0.00287099	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462101	AATTTGCAGAAAGAT[A/G]CCACTGCCTCATTTA	143279
rs748414092	snp	A/G	4.29387e-05	0.00463331	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425401	CTTGTTTTCCCTAAC[A/G]TCAAGAATGGTAAAT	143279
rs748421369	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500114	ACACAAGACAGACTA[C/T]AACCAAGTGCCCAAA	143279
rs748455082	snp	C/G	6.62142e-05	0.0057535	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484614	CTATAACAAAGTGTT[C/G]CTGGTGGATTCCATC	143279
rs748465110	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422068	TTCCCTAGACTGCTA[C/T]CATAGTGATTTTTTT	143279
rs748471839	in-del	-/CT			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496824	CATGCTATTATTTAC[-/CT]TTTTCTAATAATTTA	143279
rs748503667	in-del	-/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91453723	ACATTAAATGTAAAT[-/G]GTCTAAATAAAAGAT	143279
rs748515065	snp	G/T	1.96775e-05	0.00313662	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500473	CCATCACTCTTTAAT[G/T]ATTGTTTTTGATAAA	143279
rs748591729	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91469800	TATAAGAAGAAAGAC[A/C]AAACTATATGCTGTC	143279
rs748606930	snp	A/G	1.64974e-05	0.00287201	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499122	TTTATTATGGATTTC[A/G]TAGTGTGTGTGCTTC	143279
rs748694310	snp	A/T	1.7216e-05	0.00293389	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425235	GCAATAAAATAATTT[A/T]TAGGTAGTAGGAAGT	143279
rs748755195	in-del	-/TTT	3.42454e-05	0.00413782	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484661	GCTTTACTTAGTAGG[-/TTT]TTATTATTCTATCAT	143279
rs748755442	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91423955	CACTGGAAAAAGCTT[C/T]AGAAACAAGTTATGA	143279
rs748778519	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91488154	CCACTCAAACTACTG[A/G]AACATTTTCTAGGTT	143279
rs748792610	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509256	ATGTGCACATGTACC[C/T]TAAAACTTAAAGTAT	143279
rs748794078	snp	C/T	1.95551e-05	0.00312685	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484355	TTCAAGGTAAGATTT[C/T]GTATCTTTTCAAATG	143279
rs748825202	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471384	GAATGAGCAAAAGCT[A/G]CAAGTCTTCCTCTTG	143279
rs748836134	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450381	AAATTAACTCAAGAT[A/G]GATTAAAAACTTAAA	143279
rs748847125	snp	G/T	3.30956e-05	0.00406776	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484562	CTGCAATTTATTTCT[G/T]TACGCCTGTTTCCTG	143279
rs748868526	snp	G/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91513554	AAAAAGAAACTGCAT[G/T]TTAAGTCAGACAGTA	143279
rs748972642	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91489547	TGGGAGGAGTAGCTA[C/G]TAATCTTGTTTGCCA	143279
rs748993611	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470535	AACATACCAGAATCT[C/T]TGGGACCCAGCACTG	143279
rs749067341	snp	C/G	1.64827e-05	0.00287073	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462132	ACACCATTGAAGACT[C/G]TGGGATTAATGCTAA	143279
rs749079428	snp	A/G	1.67377e-05	0.00289284	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493430	TTTAGGCATGTTTAC[A/G]TATCACAAGGATTCA	143279
rs749085880	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450221	TCAGAAATAATGCCA[C/G]ACATCTACAGTAATC	143279
rs749099127	snp	C/T	1.64969e-05	0.00287196	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492373	CGGAAAAGAGCCGAT[C/T]TGAAAAAGAAGTTAA	143279
rs749108919	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437753	TACATTGTAAGTTTC[C/T]ATACTTCCTGAATTT	143279
rs749164105	in-del	-/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440180	AGGGAATGCTTCCAG[-/C]CTTTTGCCCATTCAG	143279
rs749176984	snp	A/G			intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91463212	ATTAACGTATATTTT[A/G]TGTTATATGTATTCT	143279
rs749262789	snp	G/T	1.73108e-05	0.00294195	synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425361	GAAGAAAGAAGCTGC[G/T]GAAAACAGAAGTTCA	143279
rs749374487	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452278	AAACCTGCAGATTCA[A/G]GAAGCTAAACAAACC	143279
rs749422558	snp	A/G	1.66485e-05	0.00288513	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500509	ATTGGCAGCTGCTTC[A/G]TCCAGAAGAGGTTGA	143279
rs749454632	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91475416	CATTCGTGAAGGAGA[C/G]ATCAAAGTGTTTAAA	143279
rs749467476	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497921	CTGGATAGTTTCCCC[A/G]TCTATGACCTATAAT	143279
rs749484971	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91436019	TTTCCCCTCTGAATC[A/T]TTCTTTTTTATAGTA	143279
rs749506503	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91495330	AGTAGTTCTGACAGT[A/G]TTGTGTTTCTAATAC	143279
rs749572469	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91453924	TTAGAACAAAGAAAA[C/G]TCATGGAGACAGAGG	143279
rs749584369	snp	A/G			intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481533	TTATTTTCCCATCTA[A/G]TAGGTTTTCACTTCA	143279
rs749620112	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509912	ACAAACCTGCACATG[C/T]ACCCCTGAACCTAAA	143279
rs749669753	snp	A/C/G	0.000151288	0.00869616	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487602	TTTTATATTGCTACA[A/C/G]GGGGTACCTTAGATT	143279
rs749702911	snp	C/T	1.64933e-05	0.00287165	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501197	ATTCTCTAGATACTT[C/T]TGGGATGTTGTGCTT	143279
rs749712318	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502385	CTTCCTCTGTAAAGC[C/G]AAAAGTCATTATGTA	143279
rs749759731	snp	A/C	1.65767e-05	0.00287891	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485310	CTCTCACAGGTATGA[A/C]CAAAAGTTCCTTTGA	143279
rs749765399	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421907	ATTATGCTTCAGACT[A/T]ACACCTGAAATCGCT	143279
rs749802202	in-del	-/TAGT			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91473851	ACAGTAGGCTATTGA[-/TAGT]TAAGTTTTGGGGGAG	143279
rs749824074	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483337	TTCACTTTTTATATA[A/G]CACATTCCTATTATT	143279
rs749922326	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477876	AAACATGTTACGCTT[C/G]GATTCTTGTTCATTA	143279
rs749924519	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438724	TCCTGTTTCTCCACA[A/T]CCTCTCCAGCATTTG	143279
rs750002389	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450319	GGGAAACTGGCTAGT[C/G]ATATGCAGAAAACTG	143279
rs750005495	snp	A/G	9.93493e-05	0.00704732	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487548	AATTATACACATACA[A/G]TCATTTTGTATATGG	143279
rs750039976	snp	G/T			intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91515134	GGCCCTTTTCCCCTT[G/T]TCCACATACCTCATG	143279
rs750047460	snp	A/T	1.65831e-05	0.00287945	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485191	ACAGATACTGCAAAC[A/T]ATTTAGTTCACCCTC	143279
rs750052499	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464567	ATAGATGTCAGCTGC[C/T]GAGACTGGCCAGGAG	143279
rs750091897	snp	A/G			intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91463080	ATGCGAGGGTTAGGG[A/G]CGCTAACCCCCTATG	143279
rs750093531	snp	A/G	1.72042e-05	0.00293288	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500658	GGGGGATGTGGAGAG[A/G]GAACAGCAGACAGTG	143279
rs750105208	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484767	TTTTAAACCATTTCT[A/G]TGAAGGAAAGAGTTG	143279
rs750114913	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91479847	CCTAATTTAATAAAT[G/T]AAAAGTGGATCTCAT	143279
rs750183468	in-del	-/AAAATTCTATAATATGATTATTATA	2.00214e-05	0.00316391	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491344	TATTAATTAAAGCTT[-/AAAATTCTATAATATGATTATTATA]AAAATCATAGTAAAC	143279
rs750199626	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91508075	GCTAGCCATATGTAG[A/G]AAGCTGAAACTGGAT	143279
rs750249477	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468490	CAGAACAAGAACTCC[A/G]GCAACTCAAAAAGCC	143279
rs750291136	snp	A/T	1.69192e-05	0.00290849	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496379	ATTATGCCTGTAAGT[A/T]TAAAGTTATTAATAT	143279
rs750346862	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437566	AGTATAAAATAATGT[A/G]CAGACATAATGTAGA	143279
rs750382676	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496593	GAGAGGCAGTAATTC[A/G]AATCCAGGCTCTGTC	143279
rs750411426	in-del	-/TGTGTGTGTGTA/TGTT			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412692	GTGTGTGTGTGTGTG[-/TGTGTGTGTGTA/TGTT]TGTATTTGTCAAAGA	143279
rs750444221	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91455095	TACCCAGTAATGGGA[A/T]GGCTGGGTCAAATGG	143279
rs750513625	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91510958	CCTCACCAGTAAAAT[A/G]AGAACAACCACTTTT	143279
rs750515159	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444489	CAGAATGTTAACACA[C/T]TATGTTAATGGAACT	143279
rs750532061	snp	G/T			missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461326	TCTAACAACGTTTGA[G/T]TCTTTCCCAGAATTA	143279
rs750543367	snp	C/T	1.66457e-05	0.00288489	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512257	TTTTTTTAATTTTTT[C/T]CCCTAGCTTACCTGT	143279
rs750555211	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91429194	TTTATTGATTTGCAT[A/G]TATTGAACCAGCCTT	143279
rs750623138	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422830	GATAGTTGTTGAATA[A/G]CTGTTAATTGAATTC	143279
rs750624397	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468243	AGAACAAAGCCAGGG[A/G]CTCGGTACCAGCACC	143279
rs750624809	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476285	TTGGTAGAATTTACA[C/T]AGGGACAGTGAATCT	143279
rs750634330	snp	A/G	1.65012e-05	0.00287234	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498131	CCATGGATTAAGTGA[A/G]CTCTTATCACATGAA	143279
rs750650460	in-del	-/A	5.17246e-05	0.00508523	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500660	GGGATGTGGAGAGGG[-/A]ACAGCAGACAGTGTG	143279
rs750685770	snp	C/T	1.81385e-05	0.00301146	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483087	AAAAAGTAAATCATT[C/T]TATGATATTAAGAAC	143279
rs750714395	snp	A/G	0.000100484	0.00708745	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481172	TAGTTGAAGTTGTCT[A/G]AGTCAGATCTCAATC	143279
rs750714923	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445356	GCCACTAGAGAGGAA[A/G]TAGTGATATAAAAAA	143279
rs750856947	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460250	TGTTGTGAGTGAAGT[A/G]GGGGAATAAGCCCTC	143279
rs750945985	snp	A/G	1.65886e-05	0.00287993	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492330	TCTTTGTTCTCCTCT[A/G]CTGTATAATATCTTC	143279
rs750954688	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91411778	GGGTTAGGGATTACC[C/G]TAGAAAATGCTTTGA	143279
rs750964878	snp	A/G	1.67458e-05	0.00289355	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425282	TTTTCTGTTTTCAGG[A/G]TTTGGACAGAGGAGC	143279
rs751019480	snp	C/T	1.65272e-05	0.0028746	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461245	ACGGTTAATGTGTTT[C/T]CATTTTAGGGAAGAT	143279
rs751079160	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91435596	CTGCCACCTCAGGCC[A/G]CTGTGATTCCTGTTC	143279
rs751162122	snp	A/G	1.65244e-05	0.00287436	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460549	CCTATCCAGCCCAAA[A/G]CTGTGAAAGACTTTC	143279
rs751205433	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461671	CTTGTGCCTCAGCCT[C/G]CTGAGTAGCTGGGAT	143279
rs751213426	snp	A/C	5.94301e-05	0.00545083	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487575	ATGGTAAAACACAAT[A/C]CAAAAGTAATGTTTT	143279
rs751277265	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437079	GATTTCTGTTTATAC[A/C]TGTTCCAGTATCTAT	143279
rs751277334	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412349	ACTTGTACTACTAGA[C/T]AAAGAGAAGAATATA	143279
rs751294716	in-del	-/ATCCTCC			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421279	TTTTCTTGAAACTTT[-/ATCCTCC]CATATTTTTAACACA	143279
rs751305129	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91466832	AAGAAGAAATGAGAT[A/G]CCAAGTCACAAAAAG	143279
rs751326261	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464235	AGAATGACCCAGTTA[C/T]ATACTGAACAACCTA	143279
rs751326541	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91423801	GCACCTATGCACAAG[A/G]TTCACTGTATGACAA	143279
rs751337407	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421447	CACATTGGAAGAATT[A/G]TCTTGTGTCACACAT	143279
rs751365800	in-del	-/TTTTTTTTTTTTT			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497465	CCTGGCTATTTTTTT[-/TTTTTTTTTTTTT]TTTTTTGGATTTTTA	143279
rs751389066	snp	C/T	0.000355303	0.0133239	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484329	TTATTTCTCATTTAA[C/T]GAAGACAGTATTCAA	143279
rs751416584	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460904	TACTGTAAAAGTTAT[A/G]TAACCATTCAAAAAA	143279
rs751426876	snp	G/T	1.69278e-05	0.00290923	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498964	AAATAGAAAAGGTAA[G/T]TTAATACCCTTTTTA	143279
rs751452107	snp	C/T	1.65334e-05	0.00287514	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498187	CAACATTTCAGGTAC[C/T]ATTAAGGGCAAGTAG	143279
rs751474019	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91453313	GTGCATGCCTGTAGT[C/T]CTAGCTACTCAGGAG	143279
rs751478897	snp	C/T	1.71722e-05	0.00293016	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461389	ACACTTTTCATTTCA[C/T]TTTTAGTTTTAAATT	143279
rs751553639	in-del	-/TCTT			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91436017	TATTTCCCCTCTGAA[-/TCTT]TCTTTTTTATAGTAC	143279
rs751563908	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467999	CCAGCTCAAGAGCAT[A/G]GAGCAATGCCACAAG	143279
rs751643614	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91459291	GCCACTCTGGAAAAC[A/C]AGTTTGGCAGTCTGT	143279
rs751651111	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91472877	ATTAAACAGCAGATT[A/G]GAGACTGCTGGAAAA	143279
rs751684855	snp	A/C	3.31466e-05	0.0040709	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492338	CTCCTCTACTGTATA[A/C]TATCTTCAAATAGCT	143279
rs751702096	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444430	CAGAAGCCCAGATGG[A/G]ATTTATTTTTAGTTG	143279
rs751724265	in-del	-/TTAAAACATTTAAACACTTTAG	1.69691e-05	0.00291278	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491318	TGAGGTATAATTTAT[-/TTAAAACATTTAAACACTTTAG]TCCAAAATGATATTA	143279
rs751767879	snp	A/G			intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482857	GGTTATTGTTATTTT[A/G]TAATCTCAAATTTTG	143279
rs751770903	snp	G/T	8.32702e-05	0.00645199	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484521	GATTGTCCCAGAAGA[G/T]GTTCAAACAATTGGT	143279
rs751771147	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419884	AGGACTCATAGATAA[C/T]GTATACAAAACTCAG	143279
rs751812903	snp	A/C	1.67058e-05	0.00289009	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425322	AATTTCCACTTTCAG[A/C]AGTTTTATTTCAGCT	143279
rs751857241	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509565	CTGGATAAAGAAAAT[G/T]TGGTACATATATACC	143279
rs751858400	snp	C/G	1.65293e-05	0.00287479	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478207	TGCCTACAGCCTCAA[C/G]ACGTTCAGAAGACAG	143279
rs751864916	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439933	TTGCACACTGATTTT[A/G]TATCCTGAGACTTTG	143279
rs751875620	in-del	-/A	1.65523e-05	0.00287678	frameshift-variant, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478251	CATTAACAGCCTGTT[-/A]CGAGAATGGAAAGGG	143279
rs751910169	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503631	CGGAGGGTCCTACCC[A/C]ACGGAGTCTCGCTGA	143279
rs751932540	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91414614	TCAGAGATGAGAGAA[A/G]GGAGATCACTGTGTG	143279
rs751966690	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91414949	GAGGAACAACATAAT[A/G]AAATCAGTGGTAGTG	143279
rs751969248	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450888	TGGAGAGGATGTGGA[G/T]AAATAGGAATGCTTT	143279
rs752001301	in-del	-/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452760	CAGATTTCTCATCAG[-/T]TAACCATGGAGGCCA	143279
rs752018378	snp	C/T	1.84035e-05	0.00303338	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493386	TTTTTAAGTCAATCA[C/T]GTTAATAATAACATT	143279
rs752022438	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91472500	ATAGCAAAAGAAACT[A/G]TCAACACAGTAAGTA	143279
rs752032086	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91454188	ATCAACCAACAGCAC[A/T]TTTACAGCACGCTCT	143279
rs752056020	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491895	GGGCTGGAGTGTAGT[A/G]GTACAATCAAAGCTC	143279
rs752071577	snp	C/T	6.91372e-05	0.0058791	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496176	ACTCATTTGTTGTCA[C/T]GGATTTTATGTTAAT	143279
rs752094365	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433552	TGGATGTACATTTGT[A/G]TTGAAGTAAGTAAAC	143279
rs752095505	snp	C/G	1.65356e-05	0.00287533	intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462216	GCAAGTAATATTATT[C/G]TGTGTCTCTTCTGTA	143279
rs752133867	in-del	-/A			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91504950	GAAACCCTACAAGCC[-/A]GAAGAGAGTGGGGAC	143279
rs752206032	in-del	-/T	0.000271124	0.01164	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512240	TTTCAAGACTTAGTA[-/T]TTTTTTTTAATTTTT	143279
rs752314653	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91435323	TATTAGATGTCTGTC[A/G]GAAAGACTCCTCCAA	143279
rs752351069	snp	A/G	0.000165027	0.00908221	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496338	CAGTAGGCATCTGCA[A/G]TGTTACCGTGGACGA	143279
rs752354222	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91474211	GAGTAGGGGAATGGG[A/G]AAAAGAAGCATTAAA	143279
rs752358342	snp	C/G	1.66056e-05	0.00288141	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492309	TGTTAATTCTCTTTT[C/G]ACTGCTCTTTGTTCT	143279
rs752363576	snp	C/T	1.6489e-05	0.00287128	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460478	AAAAACAGCGTACAT[C/T]TATGGATGCATCATC	143279
rs752371951	snp	A/C			intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91407523	GTTGCACTATTTCAT[A/C]GCTATACCTTCTAAA	143279
rs752374928	snp	C/T	1.68315e-05	0.00290094	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425336	GCAGTTTTATTTCAG[C/T]TGTTAGCCCGAAGAA	143279
rs752402638	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433870	TTTTCTGGGTTTCTG[G/T]CATGTTTACCCTGTT	143279
rs752417748	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91480455	ATCTGGTTGTCATAG[A/G]GGTGAACCATTTTCA	143279
rs752435739	snp	A/T	1.65081e-05	0.00287293	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461272	AGATGTAGAAAAAGT[A/T]AAGTCATCAGGAGAT	143279
rs752442173	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91494580	AGATTAATAAAAGAA[A/G]GTGTAGTAGGGAACA	143279
rs752545557	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492623	AATTGTTTAAGGACT[A/G]TTATTTACATTTTAA	143279
rs752583675	snp	A/T	1.65707e-05	0.00287838	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484543	ACAATTGGTAGAGAG[A/T]TTGCTGCAATTTATT	143279
rs752598261	snp	A/G	1.84677e-05	0.00303867	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484684	ATTCTATCATTTTTT[A/G]CTTTTCTTTTGTTAC	143279
rs752748359	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419543	AATAAGATTTTTGGT[A/T]AGTTATTGTAATTAC	143279
rs752764292	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471108	ATCTAAAAGCACATC[A/G]ACAAGCTAATCCACC	143279
rs752770990	in-del	-/TAA	1.7056e-05	0.00292022	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460387	TAATTTTGAAAAGTT[-/TAA]TGATTCATTATTTTG	143279
rs752773342	snp	A/G	1.69755e-05	0.00291332	intron-variant, splice-acceptor-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496204	AATGCTTAACATTTA[A/G]TATGCATAGCTTATG	143279
rs752789404	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468960	AAAAAAAAAAAAACA[A/C]GAGTACAGTTGCAAA	143279
rs752881488	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502880	ACATGAATCTAGAAC[A/C]TCTAGGATTCCCAGT	143279
rs752921165	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438886	GTCTTCTTTTAAGAG[A/G]TGTCTGTTCATATCC	143279
rs752958771	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91472244	GTGCTGGGATAACTC[A/G]CTTGCTATATGTAAA	143279
rs752989148	snp	A/G	0.00128617	0.0253265	utr-variant-5-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410418	CCGCCGCCGCCTGGC[A/G]CTCCCGCCGCCCGGC	143279
rs753008984	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457958	AAAAAGAAGAAAAAA[C/G]ACATACAGATTAGAA	143279
rs753098917	in-del	-/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437619	GGTTGGATGGTTGTT[-/C]TTTTTTTTTTTTTTT	143279
rs753110657	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425511	GATAGGTCTAGTTAA[C/T]ACAACAAAAAGAAGC	143279
rs753124341	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449484	CTTTAAGAACTGACA[C/G]AAGACAAGGACGCCC	143279
rs753142699	snp	C/G	1.65075e-05	0.00287289	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492365	AGCTAACCCGGAAAA[C/G]AGCCGATTTGAAAAA	143279
rs753153907	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91480851	GAGTTAATCATATTT[A/G]CCTCACAAAATGTTA	143279
rs753159211	snp	C/G/T	3.30482e-05	0.00406487	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501163	TTTGTCAAGACATTT[C/G/T]ATGTTAATTTCCTTT	143279
rs753170472	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483494	ACCTAAAAATGTCAT[C/T]GTAAAATATAGGCTA	143279
rs753187263	snp	A/G	1.67058e-05	0.00289009	synonymous-codon, intron-variant, nc-transcript-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481118	AAAAGATGATCTTAG[A/G]GCATATTTTATACTT	143279
rs753224625	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450749	AGAAGACATTTATGC[A/T]GCCAACAAACATGAA	143279
rs753248841	in-del	-/TT			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470333	CAATTCTCAGCAAAC[-/TT]TTAAAAAATGAATTC	143279
rs753248846	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487303	AATGATGGATTCTTA[C/T]ATTAATTTTGAGCAC	143279
rs753284503	snp	G/T	1.65974e-05	0.0028807	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499027	TACTATTTAAGAGAT[G/T]TAAAATTGCTTTTCA	143279
rs753314078	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450103	AGAACAAAGCTGGAG[A/G]CATCATTGCTACCTC	143279
rs753335126	in-del	-/GTGG/GTGTGG			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412673	TGTGGCAGAATGTGT[-/GTGG/GTGTGG]GTGTGTGTGTGTGTG	143279
rs753351745	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464805	CCTCACAGCCACTCA[A/G]CCTACCCCAGCATGG	143279
rs753401210	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432450	TAAGTGAGAAGTGTA[G/T]GAGTTTTACCTACTG	143279
rs753446077	in-del	-/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91455294	GGTATCTCATTGTGG[-/T]TTTGATTTGCATTTC	143279
rs753466237	snp	A/T	3.30229e-05	0.0040633	intron-variant, stop-lost	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462206	ATTATGACATGCAAG[A/T]AATATTATTCTGTGT	143279
rs753473384	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492073	AAAAAAAGAAATGAA[C/T]TATATTGTGCTAAAT	143279
rs753533776	in-del	-/AAG			intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91489173	TTTTCTTCTACTTTA[-/AAG]AAGGAGAATGGCAGG	143279
rs753549900	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91466538	TAATATATTCATTCA[C/G]TGCTATACATTTCCC	143279
rs753564446	snp	C/T	1.64882e-05	0.00287121	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460508	CATCCGAAATGAAGG[C/T]CCCAGTCCTTCCAGA	143279
rs753570981	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499809	TTGAATTATTTTTCA[C/T]GGGAGAGAGAAATGG	143279
rs753733326	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91479940	TTATCCTTTTATAAG[C/T]TTTCCACCTACTTTT	143279
rs753761920	snp	A/G	1.67066e-05	0.00289016	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460416	TTTGAATGTGTTTTT[A/G]TACTTCACAGTGAGA	143279
rs753772223	in-del	-/TGT	3.34997e-05	0.00409252	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512223	CAGTCATTTTGTGTG[-/TGT]TTCAAGACTTAGTAT	143279
rs753786315	snp	A/C	0.000185374	0.00962562	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487512	TGATACATTCTTCAC[A/C]TGGCTGTGAGAATTA	143279
rs753793933	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439589	TGGTTCCACATGAAA[C/T]GTAAAGTAGTTTTTT	143279
rs753796420	in-del	-/TGT			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509949	GGTAGAGGAAAAACA[-/TGT]TGTATTATATCTCAA	143279
rs753801716	snp	C/G	1.67276e-05	0.00289197	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481152	CAGGTAAGAGAACCA[C/G]AACCTAGTTGAAGTT	143279
rs753896339	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438800	TGGTATCTCATTGTG[C/G]TTTTGATTTGCATTT	143279
rs753962972	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449863	CTACAAATCACTCCT[C/G]AAGGAAATAAGAGAG	143279
rs754045734	snp	C/G			intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91488914	TGTTACTTGATCTTG[C/G]GTAGATATTGGCTCA	143279
rs754077156	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91456890	AAATTGAGAAAATCA[A/G]TGAAACAAAGAGATG	143279
rs754079781	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91446038	CACCAGTGACAGACT[G/T]CCTCCTCAAGTGGGT	143279
rs754080814	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91414146	AGGTGAACAGAAAAG[A/T]GAGGTTCTACATGGG	143279
rs754084276	snp	C/T	1.67508e-05	0.00289398	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478271	AATGGAAAGGGTAAA[C/T]TAATATTTTCAATAT	143279
rs754119874	snp	A/G	1.65343e-05	0.00287521	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496346	ATCTGCAATGTTACC[A/G]TGGACGACTTATGTC	143279
rs754153928	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425133	AGACAGTTAAGTCCT[A/G]GAAAAGGTAAGTCAA	143279
rs754169651	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91480218	TCAAACCTACTCATA[C/T]AATTTATTGTGCATG	143279
rs754169828	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440507	AGGATTTTCATATCC[A/T]TGTTCATCAGGGATA	143279
rs754229353	snp	C/T	1.69769e-05	0.00291345	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512240	TTTCAAGACTTAGTA[C/T]TTTTTTTTAATTTTT	143279
rs754263318	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91475844	CTGTGGGTGAGAGGG[C/T]TGCTTTACAGGAGAT	143279
rs754270999	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445617	CGAATAGGAACAGCT[C/T]CGGTCTGCAGCTCCC	143279
rs754306273	snp	C/T	1.71111e-05	0.00292494	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491184	AGCAAAACTGTTTAC[C/T]TTCTTATTTAATCAG	143279
rs754333950	snp	G/T	2.55607e-05	0.00357487	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410483	CGCCACTCCGCTGGT[G/T]GTGGCGGCGCCCGCG	143279
rs754347759	snp	A/C	7.80564e-05	0.00624677	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410541	GAGCGCGAGAAGCTG[A/C]CGCCCATCGTATCGG	143279
rs754364016	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91511273	CCTAAATGATGATAA[C/G]AACACTATCAGATAG	143279
rs754456656	snp	C/T	1.74184e-05	0.00295109	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496401	TATTAATATCTTGTC[C/T]TTTAATGCGAAATCA	143279
rs754458389	in-del	-/AT			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496537	TTTCCTTAGAGACAC[-/AT]GTCACCCACTTTGCA	143279
rs754474041	in-del	-/AAC	1.80055e-05	0.00300041	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493396	AATCATGTTAATAAT[-/AAC]ATTATTCGTGTGTTT	143279
rs754483584	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91418813	TATTAAAAATTGGTA[A/C]AGTAGGGTATCTTAA	143279
rs754530507	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433850	GGTAATGAATGGGAG[A/G]CACTTTTTCTGGGTT	143279
rs754621073	snp	A/C			intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91407892	CACTTGGCATAGCTA[A/C]AAAGCATCTTCTCCA	143279
rs754658726	snp	A/C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451559	TTGTGCCCCACTCCA[A/C/G]ACCTACTGAATCACA	143279
rs754675720	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501911	CTTATAATTTCTAAA[A/G]CTAACTTGAATAGAC	143279
rs754690974	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432451	AAGTGAGAAGTGTAG[G/T]AGTTTTACCTACTGT	143279
rs754717871	snp	C/T	1.66441e-05	0.00288474	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478182	TCCTAATTACCTTAC[C/T]GTTTTCTTTTGCCTA	143279
rs754729832	snp	A/G	1.65861e-05	0.00287972	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460565	CTGTGAAAGACTTTC[A/G]GTAAGTTTCAGCTAT	143279
rs754735604	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91455321	TTTCTCTGATGGCCA[A/G]TGATGATGAGCATTT	143279
rs754747620	snp	A/G	1.78058e-05	0.00298372	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491170	ATAGTCTAAGTAAAA[A/G]CAAAACTGTTTACTT	143279
rs754776715	snp	G/T	1.97311e-05	0.00314088	intron-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483111	TAAGAACTTTTATAG[G/T]CTCACAGTTTTAAGT	143279
rs754792780	snp	C/G	0.0555102	0.157079	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410601	GGGCCGGGGCCGTCT[C/G]GCGCCCCGGACGGCG	143279
rs754842127	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499985	ACTCTGGTAATTGTG[A/G]GAGTGGACAGAGGGA	143279
rs754846605	in-del	-/ACTT	1.67259e-05	0.00289183	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512231	TGTGTGTGTTTCAAG[-/ACTT]ACTTAGTATTTTTTT	143279
rs754923572	snp	C/T			intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91463434	ATGTATATAAGCAGA[C/T]TTGCACAATTCAAGC	143279
rs754958925	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438359	ATTCCTATGTTAGTT[A/T]GCTGAGAATGATGGT	143279
rs754985201	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91469634	AGGAAAGACTGTTAC[C/T]GGCTGCCACAAAAAC	143279
rs754995952	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91416702	GCTGAAAAGCTGTTT[A/G]TAAGCCAGCCAGCCC	143279
rs754999418	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425202	AATTAAAATCTCTTA[C/T]AAATGTTTGTGATTT	143279
rs755006859	snp	A/G	1.65963e-05	0.0028806	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498213	AGTAGTTATCTGTTA[A/G]TCATATATTTCATAT	143279
rs755017596	snp	A/G	1.6569e-05	0.00287824	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492340	CCTCTACTGTATAAT[A/G]TCTTCAAATAGCTAA	143279
rs755029828	snp	C/T	1.64961e-05	0.00287189	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462092	CTTAAATTGAATTTG[C/T]AGAAAGATGCCACTG	143279
rs755070377	snp	A/G	5.33509e-05	0.00516455	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493399	CATGTTAATAATAAC[A/G]TTATTCGTGTGTTTT	143279
rs755115396	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91486976	TCACTTTGAATGGCA[A/G]TCTAACTCCAGAAGT	143279
rs755117168	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91414848	AAGATTGCATGGGGG[A/C]TGGAGCCAGATCACT	143279
rs755145753	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468418	AATAAAATCCCATTC[A/G]AAGGGTAGCAACTCC	143279
rs755185969	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437832	CTTTTTGGTAGGTTT[A/G]TGAGTCTTTTCCATT	143279
rs755249489	snp	C/G			missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496214	ATTTAGTATGCATAG[C/G]TTATGGGACTAGCTG	143279
rs755277607	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444604	AAGAAAAATAACAGA[C/T]TGCAGCTGTTCTCAA	143279
rs755291321	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91511337	AGATAATTTTTACAT[A/G]TGCATCAAGGGGCAT	143279
rs755359732	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461577	GTTTTGAGATGGAGT[C/T]TCACTCTGTTGCCCA	143279
rs755406925	snp	C/T	0.00010057	0.00709049	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500466	CTTAAAACCATCACT[C/T]TTTAATTATTGTTTT	143279
rs755454672	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476674	GAGATGCTTGCCCTA[C/T]CCTGTTGCTGGCTTC	143279
rs755465778	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91475885	CTCTAGGGACACAGC[C/T]GACCCATGACAACCA	143279
rs755550125	snp	A/G	3.30786e-05	0.00406672	intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462218	AAGTAATATTATTCT[A/G]TGTCTCTTCTGTATA	143279
rs755619233	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91513524	TTTTTTAGAGTTTCT[A/G]ATAAAGTAGTATGTA	143279
rs755620123	snp	A/G			intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91463169	ACCTATTGTTGACCA[A/G]AAGTCTTACTGATAA	143279
rs755638398	snp	C/T	1.67438e-05	0.00289338	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499008	AGTATTTGCCATTTA[C/T]TTTTACTATTTAAGA	143279
rs755655747	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450892	GAGGATGTGGAGAAA[C/T]AGGAATGCTTTTACA	143279
rs755687238	in-del	-/A			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509930	CCCTGAACCTAAAAT[-/A]AAAGGTAGAGGAAAA	143279
rs755687291	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477980	ACCATATATGTTTGT[A/G]CATGTTGTATGCTAC	143279
rs755745489	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464606	TTAAACTAAAGGTCA[A/G]TGTAGCCATCAACTG	143279
rs755764457	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426369	ACAAACCTAGAAATA[G/T]TTAAGGACATAGTTT	143279
rs755814647	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450325	CTGGCTAGTCATATG[C/T]AGAAAACTGAAACTG	143279
rs755825991	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464434	ACTGGAACATGACAG[C/T]AGAAATAAGTATAAG	143279
rs755833365	snp	C/T	3.40038e-05	0.00412319	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460395	AAAAGTTTAATGATT[C/T]ATTATTTTGAATGTG	143279
rs755892571	in-del	-/AT	0.000179848	0.00948112	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491355	GCTTAAAATTCTATA[-/AT]ATGATTATTATAAAA	143279
rs755895829	snp	A/G	1.65685e-05	0.00287819	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462065	TCTTTAAAATGTTGA[A/G]TATACTTAATTCTTA	143279
rs755950427	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415027	CTCATGCCTGAGGCA[A/G]TGAGTGCATCCACTA	143279
rs755956224	snp	C/T	1.69697e-05	0.00291283	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425345	TTTCAGCTGTTAGCC[C/T]GAAGAAAGAAGCTGC	143279
rs755976398	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433227	TTTTTTCTTTTTTAT[A/T]TTAAAGATAACTTTT	143279
rs756019465	in-del	-/T	1.91701e-05	0.00309592	intron-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483103	TATGATATTAAGAAC[-/T]TTTATAGTCTCACAG	143279
rs756040551	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437707	GTAGAAATTCATAAT[C/T]AAAAATCAGTTTTTT	143279
rs756042772	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91453799	TAAGAAATTTGCTTC[A/G]AATATAACAGTATAA	143279
rs756057624	in-del	-/TTTA			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496918	TTCTATTTTTAAATC[-/TTTA]TTTATGGATAATTTC	143279
rs756059874	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476227	ATGGGATGTAGGACT[C/T]AAATGAAGGGATTGA	143279
rs756060061	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499678	CTATTTAGAATACCA[C/T]GTCAGAAGTATCATA	143279
rs756098083	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485035	CACAATTTTTAAATT[A/G]CCCCTTTCATTTGGA	143279
rs756113098	snp	A/G	1.65682e-05	0.00287817	synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484546	ATTGGTAGAGAGATT[A/G]CTGCAATTTATTTCT	143279
rs756138908	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445389	TTGCTGCTGGTTACA[C/T]GCTCTTGCAAAATGC	143279
rs756186159	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91511061	AAACACTGAGTAAAT[A/G]CTGATTCTAGTAGTT	143279
rs756191774	snp	C/T	6.73446e-05	0.00580239	intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496211	AACATTTAGTATGCA[C/T]AGCTTATGGGACTAG	143279
rs756193649	snp	A/G	1.65244e-05	0.00287436	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478237	GTATTAAAGGGAATC[A/G]TTAACAGCCTGTTAC	143279
rs756213222	snp	A/G	0.000182305	0.00954564	intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462231	CTGTGTCTCTTCTGT[A/G]TATCAAAAGCAGCCA	143279
rs756259120	snp	A/G			intron-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483193	AGAAATGATGCTTAT[A/G]TTCACAATGCTTCAA	143279
rs756334104	in-del	-/CT			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501986	AACATTCCCTAAGTG[-/CT]CTTAGTTCTTCCTTT	143279
rs756351802	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493410	TAACATTATTCGTGT[G/T]TTTTTTTAGGCATGT	143279
rs756405268	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476351	CTGTCCCAGGCAGGT[A/G]TGGAAGCCCAGAGCT	143279
rs756418242	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468272	CCCCCCAGAGTTAGA[G/T]CATGCAGCCCAGGAG	143279
rs756424015	in-del	-/T			intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462642	TGAGTTCATTTATGA[-/T]GTGACACATACTATA	143279
rs756431313	snp	G/T			upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409737	CTGTCTCCCCGGGCT[G/T]CGCAAGCTCCGGGCC	143279
rs756480887	snp	A/C	7.90952e-05	0.00628819	utr-variant-5-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410435	TCCCGCCGCCCGGCC[A/C]GACATGAGTGAGGCG	143279
rs756494938	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91473576	TTCACTCACACACAG[A/G]TTTTATTCCGCCTCT	143279
rs756500942	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91472974	GATAAACTATAAAAA[G/T]AATAAAGATGTATAG	143279
rs756550444	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444495	GTTAACACACTATGT[C/T]AATGGAACTTGAATT	143279
rs756565284	snp	A/G	5.37418e-05	0.00518344	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487578	GTAAAACACAATCCA[A/G]AAGTAATGTTTTATA	143279
rs756612400	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91494388	CATTATAAGCTGAGA[A/G]AATGGTGAGAATAAA	143279
rs756633011	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509818	ATAAAAGAAACTGCC[C/T]ATCAGGTACTTACTT	143279
rs756672955	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503974	GTCCCTGACACCTGA[C/T]CCCCGAGCAGCCTAA	143279
rs756692446	snp	C/T	1.70292e-05	0.00291793	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499200	GCTTTTGTAGTACTA[C/T]CATGTTAACAAATAA	143279
rs756722954	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451358	GGGGAACATCACACA[A/C]TGGGGCCTTTCGGTG	143279
rs756738981	snp	A/G	1.96192e-05	0.00313197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500474	CATCACTCTTTAATT[A/G]TTGTTTTTGATAAAT	143279
rs756743761	in-del	-/AG			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449873	CTCCTCAAGGAAATA[-/AG]AGAGAACACAAACAA	143279
rs756774377	snp	C/T	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450550	taaactaaagagctt[C/T]taaacagtaaaagaa	143279
rs756782847	snp	C/T	1.69674e-05	0.00291263	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485159	TGGAAAAAGTCTTTA[C/T]GTTAGAATTTATCTT	143279
rs756931681	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503423	CAGTGGGTGCGCACA[C/G]CGTGCGCGAGCCGAA	143279
rs756945924	snp	A/C			missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462175	TGTGTATGATACCTT[A/C]CTTAATACTGTAAGT	143279
rs756946583	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91414429	TGGGACAAAATGTAA[C/T]TACCAATTATTGAAC	143279
rs756980263	snp	A/C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461737	TATTTTTAGTAGAAA[A/C/T]AGGGTTTCACCATGT	143279
rs756986752	in-del	-/T	1.68454e-05	0.00290214	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478277	AAGGGTAAACTAATA[-/T]TTTCAATATTTAGCT	143279
rs756994043	snp	C/T	1.65559e-05	0.00287709	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499037	GAGATGTAAAATTGC[C/T]TTTCAGAATATGTAC	143279
rs757007563	in-del	-/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91510467	TTTTTCTTCAATAAA[-/C]ATTTTCATAAGATAT	143279
rs757044981	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451951	ATCTATAAGATATTA[A/G]TCATTCTGTTGTTTT	143279
rs757057019	snp	C/T	1.64895e-05	0.00287132	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460516	ATGAAGGCCCCAGTC[C/T]TTCCAGAACCTATTC	143279
rs757077094	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91423854	CAGCATGAAGGGCCA[A/G]CATTAGAATGATTAT	143279
rs757093456	in-del	-/AT			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498338	CCTGATAAAGTAGAC[-/AT]GTGTAGATGAGCAGT	143279
rs757106994	in-del	-/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464727	TAGTTGGAGCACACA[-/C]CCATGCTACCTGTGC	143279
rs757119831	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460934	ATCCAGATGCATATT[G/T]GAAGGACGAAGTGGG	143279
rs757131730	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91494976	TTTTTTTTGCAATAG[A/C]TATTAGTTTCTATTT	143279
rs757185915	snp	C/T	8.96355e-05	0.006694	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484675	GTTTTTATTATTCTA[C/T]CATTTTTTACTTTTC	143279
rs757244293	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509640	AGCAACATGGATGAA[C/G]CTAGAGGCTCCATCC	143279
rs757327469	snp	A/G/T	2.54709e-05	0.00356858	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410484	GCCACTCCGCTGGTG[A/G/T]TGGCGGCGCCCGCGC	143279
rs757353542	snp	A/G	1.69183e-05	0.00290841	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478283	AAACTAATATTTTCA[A/G]TATTTAGCTAATCAG	143279
rs757366550	snp	A/G	1.6492e-05	0.00287154	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501233	TCCTCTTGATCTTCA[A/G]AAGAAGTTGCTACAT	143279
rs757378952	snp	A/G	1.67265e-05	0.00289188	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481153	AGGTAAGAGAACCAG[A/G]ACCTAGTTGAAGTTG	143279
rs757393670	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91459330	TAAACATGCAACTGC[A/C]GTATATTTACCTCAA	143279
rs757445986	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421508	AGCTAAAAAGAAAAA[A/G]TCACAAAAAAAATTT	143279
rs757447021	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438689	ACTAATTTACACTCC[C/T]ACCAACAGTGTAAAA	143279
rs757449489	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419908	AACTCAGTAATAGCT[G/T]TGGTCCAAATTTCAG	143279
rs757503729	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444454	TTAGTTGAAAAGGTA[A/G]CTTAAACTGAAGAGT	143279
rs757516932	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471207	CATCACGTAACAGAA[C/T]TAAACACAAAAACCA	143279
rs757567482	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91511739	GAGGCAGAGCTCAGG[C/T]AGTAATGCTCGCCTG	143279
rs757568322	snp	A/G			intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482896	ATTTACCACGTACTT[A/G]TTAAGCTTAGTGTCT	143279
rs757593989	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491952	GGGTCTCAAGCCATA[C/T]TCCTACCTCAGCCTC	143279
rs757603421	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91489437	AAATTGGTTTCCTAA[C/G]CTAAAATAAGTTCCT	143279
rs757603762	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91414751	AGTGACGAAAACAGC[A/G]TGAGCAAGGCTTAAA	143279
rs757672508	snp	C/G	6.60284e-05	0.00574542	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461285	GTTAAGTCATCAGGA[C/G]ATTGGAAAGCAGTAC	143279
rs757787922	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91472522	CAGTAAGTAGACAAC[C/G]TGCAGAATAGGAGAA	143279
rs757793125	snp	A/G			upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409589	GGAAAGTGTGGACTG[A/G]CCGTCCAATCCTATG	143279
rs757822220	snp	C/T	9.82463e-05	0.0070081	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487549	ATTATACACATACAA[C/T]CATTTTGTATATGGT	143279
rs757865029	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476854	CTTGATCCTAGCAAA[C/G]AGGCTGCTCAGGATG	143279
rs757865040	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477183	ACAGAGCGAGACTCC[A/G]TCTCAAAAAAAAAAA	143279
rs757881240	snp	C/T			intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91407865	TGGATACCCTCACTG[C/T]TGCACGTCTGACACT	143279
rs757881491	in-del	-/T	0.000271124	0.01164	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512239	TTTCAAGACTTAGTA[-/T]TTTTTTTTTAATTTT	143279
rs757944172	in-del	-/TGTT			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91479513	ATTACTCTAGTAATC[-/TGTT]TGCATTTTCCTTCTT	143279
rs757949507	snp	A/G	1.65116e-05	0.00287324	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460444	AGAGAACCACCACCA[A/G]TTTGCCTTGATGTTA	143279
rs757968216	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451888	CCTGATTACATTACA[A/G]TAGAATTAAATTCTA	143279
rs758078567	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91435372	GTTCAATCTGTGAGG[A/T]GACCTGAGTGTCCTC	143279
rs758101038	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91411019	TCTTTCCCTTCCCCC[G/T]TCAGATTAAACAGGC	143279
rs758124377	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91474280	ACAAGTCCAAATATA[A/G]GAATAAGTAATTGAA	143279
rs758138491	in-del	-/TCTT			intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91407677	TACCTTGTAATTTTG[-/TCTT]TCTTTTTCTTCCAGG	143279
rs758168184	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91465224	TAGAAAAGGGAGATA[C/T]AAATATGGGATGAGG	143279
rs758187593	snp	A/G	1.6552e-05	0.00287676	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501145	TTACTTTATTATAGG[A/G]TTTTTGTCAAGACAT	143279
rs758242990	in-del	-/TGC			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457717	TTGTGAAAGACTGAA[-/TGC]TGCTTTTACCTTAAG	143279
rs758246799	snp	C/T	3.94065e-05	0.00443866	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482921	GTGTCTTTCCTTTTA[C/T]GTGTTAACAGAATTT	143279
rs758307742	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492667	CGAATTGTTGATCAG[C/T]TGATTCTCTTACTGG	143279
rs758342516	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451070	TAAAGACACATGCAC[A/C]CATATGTTTATGACA	143279
rs758396130	in-del	-/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490039	ATTTTTAAATATATT[-/G]TTTTTTACCTATTCA	143279
rs758401032	snp	C/G			intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91407739	CCACCCTGCCAAACC[C/G]TATTCCCCATAGGTA	143279
rs758434719	snp	C/T	1.66352e-05	0.00288398	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512259	TTTTTAATTTTTTTC[C/T]CTAGCTTACCTGTGG	143279
rs758466283	snp	A/G	3.30333e-05	0.00406393	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496249	TAACAGCATCACCTT[A/G]GATATTCGTTTCCCT	143279
rs758490846	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91434392	CCTGGCTGGTACTCA[A/C]ACGTTGTCAGTTAAG	143279
rs758509214	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500230	GCTTCATGCTGGTTT[A/T]TGGAGAAGAGTAATT	143279
rs758548644	in-del	-/AT			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438848	GATGAGCTTTTTTTC[-/AT]ATGTTTGTTGGCTAC	143279
rs758566472	snp	C/G	6.3014e-05	0.00561275	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410567	ATCGGCGGGCGCCGG[C/G]GCGACCGCGGTAGGT	143279
rs758577340	in-del	-/TAG	1.66718e-05	0.00288715	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460594	TTATATGTAAATGTA[-/TAG]TAGTCATCTGCATGT	143279
rs758579923	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439888	GCTCTCTGTTTGTCT[A/G]TATTTGGTGTATAGG	143279
rs758611192	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500900	ATGCTATCCTTGTAA[A/G]TAACAGTTTAATAGC	143279
rs758615227	snp	C/T	0.000176828	0.00940121	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410488	CTCCGCTGGTGGTGG[C/T]GGCGCCCGCGCCTGA	143279
rs758626491	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91417126	CTCTGAGAAGCTTTG[A/T]TTTCCCTATTTTTTC	143279
rs758664375	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91423554	TTTACTTTACTCATG[A/G]AAGTGTCCCTCAGGT	143279
rs758711616	snp	C/G/T	3.30492e-05	0.00406494	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462079	AATATACTTAATTCT[C/G/T]AAATTGAATTTGCAG	143279
rs758740128	snp	G/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91513154	GTAAACTAGTTACTT[G/T]TGTACTCTGTAATAT	143279
rs758749962	snp	G/T			intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91514981	CCAATATTTGAAAGA[G/T]CACACAGCTATTCCA	143279
rs758760011	snp	A/G	3.30322e-05	0.00406387	intron-variant, synonymous-codon	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462208	TATGACATGCAAGTA[A/G]TATTATTCTGTGTCT	143279
rs758895077	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445880	CTTTTTCCATGGTCT[G/T]TACAACCTACAGACA	143279
rs758907895	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91469830	CTTCAAGAGACCCAT[C/G]TCACATACAGTGACA	143279
rs758918801	snp	A/G			intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462940	TGTTACACATTTCTC[A/G]TTACATGTATTTCTA	143279
rs759001513	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426017	TTCTATTAAGAAGAA[C/T]ATGATATGTATGTAA	143279
rs759028601	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91466669	ACACTCATGTATTTA[A/C]CCAAATGAGTTAACA	143279
rs759035153	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422130	GCTTAGAAGTCCTCA[A/G]TGATTTTTCTCTATC	143279
rs759097626	snp	C/G	6.37423e-05	0.00564509	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491350	TTAAAGCTTAAAATT[C/G]TATAATATGATTATT	143279
rs759113357	in-del	-/ACAG			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503108	GGGCAAAGGACATGA[-/ACAG]ACACTTTTCAAAAGA	143279
rs759118771	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452865	ATTTTTCAGGAATGG[A/G]GGGAAGGGAAATCAA	143279
rs759123338	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460326	TGAATGTAATACAAA[A/G]TAATTCATTTGTTTT	143279
rs759149047	snp	C/T	1.6601e-05	0.00288101	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492490	CCAGATTATGGTAAG[C/T]ATGTAATCTAATTTT	143279
rs759175671	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91494684	AATTCCACAAAATGA[A/G]TAACGCTTAACAATT	143279
rs759204538	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467404	TTAGCCTTGAGAAGA[C/T]TGTCAGACCTGGACA	143279
rs759226453	snp	C/T	1.6863e-05	0.00290365	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498987	CCTTTTTAATTAAAA[C/T]GAATTAGTATTTGCC	143279
rs759235217	snp	A/G	3.40142e-05	0.00412383	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425259	AGGAAGTATACTGCA[A/G]TGTTAACTTTTCTGT	143279
rs759307355	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422110	ATATGATCATGTCAT[A/G]TCTTGCTTAGAAGTC	143279
rs759310480	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471925	TATTGCAATCAAACT[A/G]CCAATGGCATTCTTC	143279
rs759358333	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444770	TATAAATAGAGGCAA[A/G]TCTTTGTTCTATCAT	143279
rs759378603	in-del	-/ATAA			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444755	CCTCAAACTGACATT[-/ATAA]ATAAATAGAGGCAAA	143279
rs759399843	snp	C/G	1.65954e-05	0.00288053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499174	ATAACTTTAAATCAA[C/G]CTTTCGGTTAGCTTT	143279
rs759485053	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444098	TTTTTTGTGGCTCCT[A/G]TAGAGTTTTTCTTCC	143279
rs759513316	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91413500	AACTTTTAAAGCCAT[C/T]ATTATCCAGGCCCAA	143279
rs759523040	snp	A/T	3.32176e-05	0.00407526	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485325	ACAAAAGTTCCTTTG[A/T]TTATCCACCTAAATG	143279
rs759546780	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91459981	TATGATGTCCACACA[A/G]TGACAAAATTGCCTA	143279
rs759586839	in-del	-/TAA			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91474887	CAACAATTGAGGTCT[-/TAA]TGATGAAAATAACTG	143279
rs759618852	in-del	-/G			upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409536	CGGGAAGGGAGAGGC[-/G]GATTTGGCAGTCAAA	143279
rs759672008	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91486967	TCACTGTAGTCACTT[C/T]GAATGGCAATCTAAC	143279
rs759676892	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91514561	ATTATTGATTTTTGT[A/G]TCTGCCACAGTAAAT	143279
rs759697775	snp	A/T	1.7093e-05	0.00292339	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460376	CTTGTATTTTATAAT[A/T]TTGAAAAGTTTAATG	143279
rs759740636	snp	C/G	1.80127e-05	0.003001	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484676	TTTTTATTATTCTAT[C/G]ATTTTTTACTTTTCT	143279
rs759835696	in-del	-/TAAATAATTTAA	3.95194e-05	0.00444501	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487826	CTATAATCAGTATAG[-/TAAATAATTTAA]TAAATAATTTAAATG	143279
rs759858666	snp	A/G	1.71352e-05	0.00292699	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481057	GCTATGAGATTAAAC[A/G]TTCATCCATAATAAA	143279
rs759883507	snp	A/G/T	2.21496e-05	0.00332781	intron-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483125	GTCTCACAGTTTTAA[A/G/T]TTTGGTATTAGTAAT	143279
rs759890574	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450025	CAGAATTAGAAAAAA[A/C]TACTTTACATTTCAT	143279
rs759911720	snp	A/T	1.6528e-05	0.00287467	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478208	GCCTACAGCCTCAAG[A/T]CGTTCAGAAGACAGT	143279
rs759960487	in-del	-/TCATCTC			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426687	TCTATACTAATATCT[-/TCATCTC]TGAAGTCAGTTCGCC	143279
rs759961686	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476816	ACCTGTGAGGCCTTT[G/T]TCTTTGGCTGGGGTG	143279
rs759965012	snp	A/T	1.72579e-05	0.00293746	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496184	GTTGTCATGGATTTT[A/T]TGTTAATGCTTAACA	143279
rs760042125	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91494001	ATAGTATTATTTTAT[A/G]GTATTTTTAAAAATT	143279
rs760051607	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464250	TATACTGAACAACCT[A/G]TTGGGGAACCAAATC	143279
rs760139680	snp	C/G			intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462867	TACTGTATCCTTTTA[C/G]GTACCTAGGTCTTCT	143279
rs760154143	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91479130	TGAGGCAGGAGAGTC[A/G]TTCGAATCCTGGAGG	143279
rs760159467	in-del	-/GTAC	0.000318319	0.0126118	frameshift-variant, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410456	AGTGAGGCGGTTCGG[-/GTAC]GTACCCTCGCCCGCC	143279
rs760179188	snp	C/G	1.67108e-05	0.00289052	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492514	TAATTTTTATAAACT[C/G]TGTTTCTTCATAATT	143279
rs760203087	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457720	GTGAAAGACTGAATG[C/T]TTTTACCTTAAGTTT	143279
rs760218786	snp	C/T	1.88021e-05	0.00306606	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493536	CTTTCCACTAGGAGG[C/T]GCTAATAGATTAGAG	143279
rs760260361	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439566	GTCTTGGCTATACAG[G/T]CTCTTTTTGGTTCCA	143279
rs760274736	snp	A/C	3.30087e-05	0.00406242	intron-variant, stop-gained	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462202	AAGTATTATGACATG[A/C]AAGTAATATTATTCT	143279
rs760295613	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419248	TGATGGAAAACCATG[A/G]TTGTTATTCTTATTG	143279
rs760325031	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420739	TGCTATTCTCTTTTA[G/T]CTAGTCAGTCTTTTC	143279
rs760336208	in-del	-/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437544	ACTCCATCCTTTGTT[-/G]GGGGGGAGTATAAAA	143279
rs760350962	snp	A/T			intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481608	TAAAAGGTTTTTTTT[A/T]AATTTGTTATAAAGC	143279
rs760441128	snp	A/G	1.6574e-05	0.00287867	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500603	TGGCTATGCAAAAAC[A/G]GACTTAACTATAAAG	143279
rs760441209	in-del	-/TACTGCTAA	1.77379e-05	0.00297802	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501373	TTTAAATCTAAAGGT[-/TACTGCTAA]TACTGCTAATACTGC	143279
rs760443090	snp	A/G	1.99031e-05	0.00315454	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484698	TACTTTTCTTTTGTT[A/G]CATTTTAGGGATATT	143279
rs760494442	snp	A/G	5.00129e-05	0.0050004	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485348	CCTAAATGAAATACT[A/G]TTCAAAAGAATGACT	143279
rs760613873	in-del	-/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450475	CGTGGGCAAAGACTT[-/C]ACGGCTAAAACACCA	143279
rs760707604	in-del	-/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445833	GAGAGACTGTGCCCT[-/G]AGGAACGGTGCACTC	143279
rs760748071	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450638	CCATCTGACAAAGGG[C/T]TAATATCCAGAATCT	143279
rs760782622	snp	A/G			intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482802	TTTCACTGTATAGCC[A/G]CAGTGTAAATGAAAG	143279
rs760890999	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91514140	ACAAAAGAAACATGT[A/G]TAAGAAACCAGATTT	143279
rs760953826	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91486803	AGAACTCTCAACTTT[C/T]ATTAACAATTTTGTC	143279
rs760986640	snp	A/G	1.96524e-05	0.00313461	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410517	GAGGAGAGGAAAGGG[A/G]AGGAGTCAGAGCGCG	143279
rs761015822	snp	A/G	1.64885e-05	0.00287123	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460498	GATGCATCATCATCC[A/G]AAATGAAGGCCCCAG	143279
rs761022848	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461423	CAAAAATGATAAATT[G/T]ACCTCATTTTCTACC	143279
rs761078485	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426494	TTCTACATTCTTATA[C/G]GTTAGTATTTTTATT	143279
rs761085462	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91435168	TATAAAAGCCCCAGG[A/G]AACCCACCCCAATCA	143279
rs761089476	snp	A/G	1.66913e-05	0.00288883	missense, intron-variant, nc-transcript-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483036	CAGATAGCTACCTTA[A/G]TGGAAGCTGACCATC	143279
rs761094636	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496056	ATTATGTAAAATAAA[C/G]GGGAAATAAATGAAA	143279
rs761124941	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91436515	TGTTTACTGCCACTA[G/T]GTCTTGGTATAGTTT	143279
rs761128980	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91506772	CTCCCTAACTCATTT[G/T]ATGAGGCCAACATCA	143279
rs761151174	snp	C/T	3.34007e-05	0.00408647	synonymous-codon, intron-variant, nc-transcript-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481127	TCTTAGAGCATATTT[C/T]ATACTTTTACAGGTA	143279
rs761159164	in-del	-/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91417144	CCCTATTTTTTCTCC[-/T]TTTTTTTATAGTTTT	143279
rs761168414	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421958	TTGGCCCAGGCTGTC[A/G]TTCCTCTTCATTCCC	143279
rs761177607	snp	A/G	1.6563e-05	0.00287771	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498074	AGCTAATGCTATTCT[A/G]TTGAAAAAATCATTA	143279
rs761202944	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476634	CAAACGGGACTTGGC[A/C]AGGAAGGCCAGCATT	143279
rs761247099	in-del	-/CAGA			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476528	TTCTCAGAAACAGGG[-/CAGA]CAGAGCAAGAGGGAG	143279
rs761264676	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499240	ATTTTAGTAGATAAG[C/G]TTTTAAAATAGAAAA	143279
rs761283869	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91411829	CTTGGAGACCTGGTT[C/G]CTGCTGCTGGTACCC	143279
rs761285804	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91430193	GTTGAGCAGTTTTGA[A/G]TGAGTTTCTTAATCC	143279
rs761344141	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91488133	GGCAGAGTGTCATTA[A/G]GCAAACCACTCAAAC	143279
rs761433244	snp	C/T	1.65483e-05	0.00287644	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478198	GTTTTCTTTTGCCTA[C/T]AGCCTCAAGACGTTC	143279
rs761498644	snp	A/G	1.65386e-05	0.00287559	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487707	TGTCAGTACCCATTC[A/G]TTATTTCTGTAGCTG	143279
rs761588632	snp	C/T	1.71728e-05	0.00293021	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501349	GGTAAATTTCTGGAT[C/T]TAATTTTATTTTAAA	143279
rs761671544	snp	C/T	1.79913e-05	0.00299922	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487538	AATTAAAAGAAATTA[C/T]ACACATACAATCATT	143279
rs761783607	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470610	AGATCTCAAGTAAAC[A/T]TAATATCACACCTAG	143279
rs761819653	in-del	-/T	1.66829e-05	0.00288811	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499017	CATTTACTTTTACTA[-/T]TTAAGAGATGTAAAA	143279
rs761856606	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91473830	TTATTGGTGAGGTTC[C/T]GATCAACAGTAGGCT	143279
rs761859807	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460204	GCTCTATATTAAGTA[G/T]GCACATCCATGTAAG	143279
rs761860123	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91424228	CTCAGAAATGACAGA[C/T]GTCTTTTCCACTTGT	143279
rs761895095	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91479492	TAATGATCTTTTTCT[A/T]AGTTTATTACTCTAG	143279
rs761919692	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91475567	GACTTTAATATGCCT[A/G]TTTGGAATGAGTTGA	143279
rs761944725	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421144	TTTGTATAGTCCGTG[C/T]CACCACCATTACCCT	143279
rs761961266	snp	A/T	3.303e-05	0.00406373	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498102	TTAACAGATTTCTTT[A/T]TATAGGAGTTGGCCC	143279
rs761991817	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91411646	TTTCAAAAATGTCTG[A/C]GGGCCCTGATAACTG	143279
rs762012583	snp	A/G	1.75844e-05	0.00296511	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498880	CCATCAGGTTTTTCA[A/G]GAAGAATTTGGAATA	143279
rs762027717	in-del	-/CATTTAAAC	3.45006e-05	0.00415321	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491324	ATAATTTATTCCAAA[-/CATTTAAAC]ATGATATTAATTAAA	143279
rs762055828	snp	C/G	1.65111e-05	0.0028732	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461264	TTTAGGGAAGATGTA[C/G]AAAAAGTTAAGTCAT	143279
rs762074168	snp	A/G	1.65523e-05	0.00287678	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461337	TTGATTCTTTCCCAG[A/G]ATTAAATGCTGCATT	143279
rs762184296	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91413509	AGCCATCATTATCCA[C/G]GCCCAAATGCAGTAT	143279
rs762285811	snp	A/C	0.000165276	0.00908903	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410542	AGCGCGAGAAGCTGC[A/C]GCCCATCGTATCGGC	143279
rs762321848	snp	A/T	1.70426e-05	0.00291908	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484481	AATGTGAATTTTGAT[A/T]GCAATTATTTTGAAA	143279
rs762361924	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91435071	ATGTGTTATACATGC[A/G]GAAGACTATAATCAA	143279
rs762396393	in-del	-/CAT			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452332	ATCCACAGCAAGAAA[-/CAT]CATAATTAAACTTGT	143279
rs762398962	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491410	TGTATGCCAATAAGT[G/T]TGCTTCCTTAAATTC	143279
rs762424278	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91453120	AGCGTGGTTCTAAAT[G/T]TATGTAAAGGAAATA	143279
rs762429126	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91486293	TGGGCACCCTAGTCC[A/C]AGATGGATATTTTCT	143279
rs762525687	snp	A/G	1.759e-05	0.00296558	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501369	TTTATTTTAAATCTA[A/G]AGGTTACTGCTAATA	143279
rs762526209	snp	A/C	4.70765e-05	0.0048514	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410494	TGGTGGTGGCGGCGC[A/C]CGCGCCTGAGGAGAG	143279
rs762530736	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437039	CTTTAACAGATAAGG[A/C]GTATGAGATTCTGAG	143279
rs762552718	snp	A/G	1.66771e-05	0.00288761	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487773	CAGATGATAAACATC[A/G]CAAGGGTAAGTCAGC	143279
rs762567056	in-del	-/TT			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431059	TTCCTTCAGGAGCTC[-/TT]TTAGGGCAGGCCTGG	143279
rs762580338	snp	A/C	1.66098e-05	0.00288177	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512400	CCTAGAAGACTTGAA[A/C]TATAATCTTTTATAT	143279
rs762589145	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467815	TTGCTGCCCCCACTG[G/T]CATGTGGGCACCCAA	143279
rs762670577	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498413	CTCTAGGCAATTACA[C/T]ATCCCCTTGAGTTGG	143279
rs762677884	snp	C/T	1.65031e-05	0.00287251	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498152	ATCACATGAAGGCAA[C/T]GTTGAAGAAGATTTC	143279
rs762737264	snp	C/T	1.76095e-05	0.00296723	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491331	TATTCCAAAATGATA[C/T]TAATTAAAGCTTAAA	143279
rs762790788	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91510422	CATGTTATTGAAGCC[C/T]CTGATGGATTAAGAA	143279
rs762896478	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422227	CCAGTCATATCTTGC[C/T]GGACCATTCTCCCTT	143279
rs762955604	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484137	ATGTGCATGTCAGGA[G/T]ACTAACATCTTTCAC	143279
rs763021803	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421041	GCATTCTTCCCCCCC[C/T]CAGGCTTTTTTCCCC	143279
rs763025125	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91513094	GACTAATTGGATTCA[A/G]GGTTATATTCTTTTA	143279
rs763071909	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91416819	GCCTTTATAAACCTC[C/T]ACCGTCCCCCTCACC	143279
rs763085497	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91456824	AAGAGAAAATCAACC[A/G]AAAGCAAGCAGGAAG	143279
rs763089260	snp	A/G	1.67105e-05	0.0028905	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425287	TGTTTTCAGGGTTTG[A/G]ACAGAGGAGCCAAAG	143279
rs763090352	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491797	CAGCTAGATCTTAAT[A/G]TGGTTATTAGAAGAT	143279
rs763099258	in-del	-/C/CATTTAAAAC	8.46423e-05	0.00650499	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491316	GATGAGGTATAATTT[-/C/CATTTAAAAC]ATTCCAAAATGATAT	143279
rs763160355	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91414380	ATGAGAAGTTGGCTT[A/T]TCAGTTGTGTATAAA	143279
rs763160910	snp	C/T	5.01132e-05	0.0050054	synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484643	TCAGCCGCTAAAGTG[C/T]TGGCTTTACTTAGTA	143279
rs763165560	snp	A/G	5.10843e-05	0.00505366	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498920	TATAATTTAAAGCCC[A/G]GTGGTGATAAAATTT	143279
rs763288841	snp	G/T			upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409245	TCCCCGCCGCTCCAG[G/T]AGACTGAGAAAAAGG	143279
rs763315961	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91418947	AAAAAGTAGTTTTTA[C/T]ATGCATCACAGATTC	143279
rs763338313	snp	A/G	4.5527e-05	0.00477089	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493558	AGATTAGAGATTTTT[A/G]AAGATTTTATCTGTA	143279
rs763353296	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464451	GAAATAAGTATAAGG[C/T]ATAAGATAATTATCC	143279
rs763433122	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91479622	TGGTTGTTTATGTGA[A/C]TAATTCCACAGTGAA	143279
rs763481650	in-del	-/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496162	ATGCATAATTCAGAA[-/C]TCATTTGTTGTCATG	143279
rs763493883	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432400	GTGGATCACATGACT[A/C]GGTATGCCTGTCAAA	143279
rs763497809	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451290	AAAACCGAACACCAC[A/G]TGTTCTCACTCATAA	143279
rs763542275	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91435527	TCTTGGTGATGACAA[A/G]TATCAACATTGCTAA	143279
rs763610868	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91454761	TGTGTAATGTTCCCC[G/T]TCCTGTGTCCAAGTG	143279
rs763618254	in-del	-/T	5.7985e-05	0.00538416	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498831	CAAAGTATGTTATTA[-/T]TATCAACCATATTAA	143279
rs763626640	snp	A/T	0.00137644	0.0261978	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498998	AAAATGAATTAGTAT[A/T]TGCCATTTACTTTTA	143279
rs763699169	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431352	TGAATCTGACAATTA[C/T]GTGTTTTGGAGTTGC	143279
rs763737968	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437062	ATTCTGAGAGATTAC[A/G]TGATTTCTGTTTATA	143279
rs763753986	snp	A/G	3.30169e-05	0.00406293	intron-variant, synonymous-codon	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462205	TATTATGACATGCAA[A/G]TAATATTATTCTGTG	143279
rs763759363	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444968	TTTAGCTGGTTGCTT[A/G]GAAACATTAAGTAAA	143279
rs763792046	snp	A/G	1.64882e-05	0.00287121	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460505	CATCATCCGAAATGA[A/G]GGCCCCAGTCCTTCC	143279
rs763797010	snp	C/T	1.68459e-05	0.00290219	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492531	GTTTCTTCATAATTG[C/T]TAGAGTGAAGTAGTC	143279
rs763827980	snp	C/T	1.66743e-05	0.00288736	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485349	CTAAATGAAATACTA[C/T]TCAAAAGAATGACTA	143279
rs763954383	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422300	GTTGCTTAGTCTTAG[A/G]TAACATTCATGACAG	143279
rs763973629	in-del	-/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460332	TAATACAAAATAATT[-/C]ATTTGTTTTCTGTTC	143279
rs763996303	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444285	TTTATTAATACCATG[C/T]TGAGGTGGAAGAGTG	143279
rs764005903	snp	A/G	0.000615277	0.0175288	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499180	TTAAATCAAGCTTTC[A/G]GTTAGCTTTTGTAGT	143279
rs764014893	snp	A/C			intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482553	GGTTTTTTGCTTTTA[A/C]TTGGATGATAGTGAT	143279
rs764016881	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91510463	ACATTTTTTCTTCAA[C/T]AAACATTTTCATAAG	143279
rs764060856	snp	A/T	3.42243e-05	0.00413654	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485140	GAATGAATCTTGTAC[A/T]TGTTGGAAAAAGTCT	143279
rs764068645	in-del	-/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497127	ACCGTGCCCGGCAAA[-/T]TTTTTTTTTTTTTTT	143279
rs764095680	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91473726	ATATATTTTCTCGTG[A/G]TTTTCTTAATAACAT	143279
rs764182279	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91472392	ATTCTGGACATAGGC[C/T]CTAGCAAAGATTTCA	143279
rs764257116	snp	G/T	1.67503e-05	0.00289393	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496216	TTAGTATGCATAGCT[G/T]ATGGGACTAGCTGTT	143279
rs764306420	in-del	-/AT			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477550	GGAATGCTATATTAA[-/AT]ATATATATACGTATA	143279
rs764326398	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91511070	GTAAATGCTGATTCT[A/G]GTAGTTTTAAGTCTT	143279
rs764371610	snp	G/T			intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91515073	TTGGCCGTAGATAGA[G/T]AACTTCAGCTCTTAA	143279
rs764376822	in-del	-/A	1.65483e-05	0.00287644	splice-acceptor-variant, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478198	TTTTCTTTTGCCTAC[-/A]AGCCTCAAGACGTTC	143279
rs764385168	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91442872	TCTTCTGCTTGATCA[A/G]TTCAGCTATTGATAC	143279
rs764406314	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464509	TCTCAGACTCCTGGC[C/T]TCAAGCAGTCCTCCT	143279
rs764482557	snp	A/G	0.000325098	0.0127453	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410519	GGAGAGGAAAGGGAA[A/G]GAGTCAGAGCGCGAG	143279
rs764506596	snp	C/T	1.65416e-05	0.00287586	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498084	ATTCTATTGAAAAAA[C/T]CATTAACAGATTTCT	143279
rs764535748	snp	A/G	6.24805e-05	0.00558895	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410455	TGAGTGAGGCGGTTC[A/G]GGTACCCTCGCCCGC	143279
rs764559672	snp	A/G	1.66949e-05	0.00288915	synonymous-codon, intron-variant, nc-transcript-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483038	GATAGCTACCTTAGT[A/G]GAAGCTGACCATCAT	143279
rs764573620	snp	A/G			upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409878	GGGCGCTTGCCCGCG[A/G]GACTCGGCGCCGCAG	143279
rs764594305	snp	A/G	1.71891e-05	0.00293159	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500657	TGGGGGATGTGGAGA[A/G]GGAACAGCAGACAGT	143279
rs764631054	in-del	-/GTGA			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91488713	TTCAGTTCCCAGAAG[-/GTGA]GTATTTCTTTCTATC	143279
rs764666436	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467405	TAGCCTTGAGAAGAC[C/T]GTCAGACCTGGACAG	143279
rs764704035	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451320	AGTGGGAGTTGAACA[A/G]TGAGAACACAGGTAC	143279
rs764770523	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91466701	TTTATGTTCACCCAA[A/G]AACCTGCACACAAAT	143279
rs764949069	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91494389	ATTATAAGCTGAGAG[A/G]ATGGTGAGAATAAAA	143279
rs764972148	snp	A/G	3.51253e-05	0.00419063	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499202	TTTTGTAGTACTATC[A/G]TGTTAACAAATAATT	143279
rs764999245	snp	C/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91513637	ATATTGCCAAACCAA[C/G]ACTTCTCTACCATAC	143279
rs765011132	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492594	AGACTTTTTGTCCAT[C/T]GTAAATGTTGAATAA	143279
rs765051775	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410880	GAGAATGACCTGCAT[C/T]TTGAGTCGGCATGAT	143279
rs765071940	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439864	GAATGGGAGTTCACT[C/G]ATGATTTGGCTCTCT	143279
rs765078736	snp	A/G			intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482112	AGATTTTAGGTGAGT[A/G]TATTGGTCAGCCATA	143279
rs765086930	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444134	ACCAGGCTTACTTAC[C/G]CTTTCTTATCCCTTC	143279
rs765112994	snp	C/T	1.64961e-05	0.00287189	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460526	CAGTCCTTCCAGAAC[C/T]TATTCTTCCTATCCA	143279
rs765142750	snp	A/C			upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91408969	TTATCTCATGATGCA[A/C]CATAACTAGTATTTA	143279
rs765187418	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432280	GGACCTATGCTGGGT[A/G]TTCTCTAACAGCTTG	143279
rs765318887	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438447	TAGTATTCCATGGTG[C/T]ATATGTGCCATATTT	143279
rs765335779	snp	A/G			intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91489034	GTCTATGATTTTTTT[A/G]TATTTGTAAGAAAAT	143279
rs765355366	snp	A/C	0.000167294	0.00914434	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410546	CGAGAAGCTGCCGCC[A/C]ATCGTATCGGCGGGC	143279
rs765358067	snp	A/G	7.0538e-05	0.00593835	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483081	TGGTTTAAAAAGTAA[A/G]TCATTCTATGATATT	143279
rs765389506	snp	C/T			intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91407530	TATTTCATAGCTATA[C/T]CTTCTAAAATTAAGG	143279
rs765400670	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502749	TTTATATTAAAAACA[C/T]TTCCAATTTTAAAAG	143279
rs765410607	snp	A/G	1.69951e-05	0.00291501	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484485	TGAATTTTGATTGCA[A/G]TTATTTTGAAATCTT	143279
rs765455667	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450723	AAGGATATGAACAGA[C/G]ACTTCCCAAAAGAAG	143279
rs765462321	snp	C/G	3.31928e-05	0.00407373	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492323	TCACTGCTCTTTGTT[C/G]TCCTCTACTGTATAA	143279
rs765494652	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91472196	GACAAAGTCCACAAA[A/G]TAATAGGGAAAAGAT	143279
rs765521364	snp	A/T			intron-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483173	TTAAATATTTTCAGG[A/T]CTTTAGAAATGATGC	143279
rs765544344	snp	A/T	3.38392e-05	0.00411321	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496378	AATTATGCCTGTAAG[A/T]ATAAAGTTATTAATA	143279
rs765637235	snp	A/G			intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91463000	TTTTATTTTCCAATT[A/G]TGACTAATATATGGA	143279
rs765641725	in-del	-/A			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91495774	CTGTTCTTCACACAT[-/A]AGTCTGTTTTTAATT	143279
rs765643302	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91414227	GATTTGACTTAGGTC[A/G]GAGAGGTGAAGAGAA	143279
rs765691512	in-del	-/TTTTTTTTTTTTTTTT			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91441886	GATTGCAACCCTTGC[-/TTTTTTTTTTTTTTTT]TTTTTTTTTTTTTTT	143279
rs765712705	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91514568	ATTTTTGTATCTGCC[A/G]CAGTAAATTAAAGCA	143279
rs765753164	snp	C/G	1.68165e-05	0.00289965	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487785	ATCGCAAGGGTAAGT[C/G]AGCTATAAAAACATA	143279
rs765806337	snp	A/G	1.65605e-05	0.0028775	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461233	CTATATGTATATACG[A/G]TTAATGTGTTTTCAT	143279
rs765833578	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464410	TACTTGATTTTACCA[A/G]GGTATTTCACTGGAA	143279
rs765834388	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426896	GGGTACATGTGCACA[A/T]TGTGCAGGTTAGTTA	143279
rs766017874	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91466307	ATTTTCTCACTTCCT[G/T]TTGTGATTAGTCTGG	143279
rs766051844	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450898	GTGGAGAAATAGGAA[C/T]GCTTTTACACTGTTG	143279
rs766112176	snp	A/G	1.65332e-05	0.00287512	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501156	TAGGATTTTTGTCAA[A/G]ACATTTGATGTTAAT	143279
rs766135854	in-del	-/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420750	TTTAGCTAGTCAGTC[-/T]TTTCTATATTCCCCT	143279
rs766135930	snp	C/T	3.30082e-05	0.00406239	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498154	CACATGAAGGCAATG[C/T]TGAAGAAGATTTCTA	143279
rs766172294	snp	A/G	3.53238e-05	0.00420246	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501371	TATTTTAAATCTAAA[A/G]GTTACTGCTAATACT	143279
rs766184441	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433888	TGTTTACCCTGTTGG[A/T]ATGTCAAACCCATCT	143279
rs766220437	in-del	-/TG	3.35272e-05	0.0040942	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512217	GCATAGCAGTCATTT[-/TG]TGTGTGTTTCAAGAC	143279
rs766229870	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457766	ATGTCTGCTCTCAGC[A/C]CTCTTATTCAACATG	143279
rs766242556	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470929	TCCCTAATTCATTTT[A/G]TGAGGCCAGCATCAT	143279
rs766287254	snp	A/C	5.0974e-05	0.00504821	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461377	TATACATAAAACACA[A/C]TTTTCATTTCACTTT	143279
rs766405215	snp	G/T			intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462624	CCAGGATATGTTGAT[G/T]TATGAGTTCATTTAT	143279
rs766408553	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422844	AACTGTTAATTGAAT[C/T]CTTAATTTTTATTGT	143279
rs766419573	snp	A/T	0.000107747	0.00733907	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491334	TCCAAAATGATATTA[A/T]TTAAAGCTTAAAATT	143279
rs766427897	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458791	ACTTTTAGAAAAAAA[A/G]TGAAACGATCTTTGG	143279
rs766467052	in-del	-/AA			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468959	AAAAAAAAAAAAAAC[-/AA]GAGTACAGTTGCAAA	143279
rs766476579	snp	G/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512632	GTCCAGTTCCTCTTT[G/T]ATATAGCACTTTATC	143279
rs766501612	snp	A/G	1.6949e-05	0.00291105	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498949	TTCAGTTACCAATCA[A/G]AATAGAAAAGGTAAG	143279
rs766610854	snp	A/G	5.00079e-05	0.00500015	synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425301	GGACAGAGGAGCCAA[A/G]GGCCAAATTTCCACT	143279
rs766614731	in-del	-/AT			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91474740	GGTTACAGATAGAAA[-/AT]AAATGTGAAAACAAA	143279
rs766616300	snp	A/T			intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91488874	CTGAAGAATGAGTTT[A/T]AACAGGTATATTCAG	143279
rs766701760	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91435261	TGAATGAGTCCTGAG[A/G]AGCAAAGGACACCTC	143279
rs766702675	snp	C/T	1.93985e-05	0.0031143	intron-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483108	TATTAAGAACTTTTA[C/T]AGTCTCACAGTTTTA	143279
rs766705769	snp	C/T	1.65247e-05	0.00287438	intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462211	GACATGCAAGTAATA[C/T]TATTCTGTGTCTCTT	143279
rs766725010	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91436681	CTAGGGAGCTAACTT[C/T]TTATTCAGTTTTTAC	143279
rs766753910	snp	C/T	3.36163e-05	0.00409963	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484504	TTTTGAAATCTTTAC[C/T]AGATTGTCCCAGAAG	143279
rs766816076	snp	A/C			utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91514634	GTCCTTTTTTAAAAT[A/C]TTTGCTTAGTCAGTC	143279
rs766816730	in-del	-/GCC	7.22935e-05	0.00601178	cds-indel, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410399	CCCAGCAACACTGAG[-/GCC]GCCGCCGCCGCCTGG	143279
rs766869355	in-del	-/A			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501444	AAGTTATTTTCATAG[-/A]AAAAATCTTCAGAGT	143279
rs766869638	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496089	GGGGAAAGGAAATAT[C/G]TGATACTAATTAGAA	143279
rs766908966	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461531	AATATTATATAAGTA[G/T]ATGGGTTTTTTGAGG	143279
rs766909985	snp	A/C	7.4438e-05	0.00610028	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493376	CACTTTGATTTTTTT[A/C]AGTCAATCATGTTAA	143279
rs766921253	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91414064	GAAAGAAGAAAATGC[C/T]TAGAGGTGGGGCAGA	143279
rs766958743	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501184	AATTTCCTTTGGTAT[C/T]CTCTAGATACTTTTG	143279
rs766964526	in-del	-/AAATT			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496866	TTAATTTTTTCATAA[-/AAATT]AAATTGAAAATTTTG	143279
rs766987264	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437199	GATCAGTGGGGAAAG[C/G]TCATCTTGGTTCTCC	143279
rs766994851	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477771	TATTATCTAAATGTA[C/T]TTTATTTTCATTTAT	143279
rs767014904	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438521	AGTCTTTGCTATTGC[A/G]AACAGTGCTGTAATA	143279
rs767046615	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499360	AGTTCATTTTCTCTC[C/T]CCTTCTACTAAGTCT	143279
rs767124323	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437100	CAGTATCTATTGAAT[A/G]TATAATAATAAACCT	143279
rs767135114	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91488153	ACCACTCAAACTACT[A/G]AAACATTTTCTAGGT	143279
rs767246912	snp	C/T	4.98136e-05	0.00499042	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499175	TAACTTTAAATCAAG[C/T]TTTCGGTTAGCTTTT	143279
rs767268111	snp	G/T	1.7367e-05	0.00294673	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491178	AGTAAAAGCAAAACT[G/T]TTTACTTTCTTATTT	143279
rs767269495	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91424298	AGAGAATGGGGAATT[G/T]AGTGAGCATAAATGC	143279
rs767288953	snp	A/G	1.66018e-05	0.00288108	synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484531	GAAGAGGTTCAAACA[A/G]TTGGTAGAGAGATTG	143279
rs767310206	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464870	TTAATATGTTATATA[A/T]GTTAAAAAATTAAAT	143279
rs767321332	snp	C/G	1.66095e-05	0.00288175	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492304	AAAAATGTTAATTCT[C/G]TTTTCACTGCTCTTT	143279
rs767348192	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468427	CCATTCGAAGGGTAG[C/T]AACTCCAGAAACTGA	143279
rs767361632	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422693	CTTTAATTTACCAAT[A/G]TTATGCAAATTACAT	143279
rs767364006	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91469234	ACTAGAGAAGCCAAC[A/G]TTCAAATTCAGGAAA	143279
rs767397945	in-del	-/A			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499369	CTCTCCCCTTCTACT[-/A]AAGTCTTTTAGAGCT	143279
rs767438083	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502364	AAAGACACAGTTTAA[C/T]GTTGACTTCCTCTGT	143279
rs767441632	in-del	-/CCTC			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437011	TCTTAACCTGAAAAA[-/CCTC]CCTTTGTTTCTTTAA	143279
rs767441856	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91486676	TTGAGAACCCCTGTC[C/G]TAAAGTACATAGTAA	143279
rs767451846	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468195	AGACCTCAGCCCTTT[C/T]GGCACAGCAGGTTCC	143279
rs767500137	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91479574	AACTTAGAATAGGAA[A/T]GTACTGTAATTTACC	143279
rs767537333	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444485	CATGCAGAATGTTAA[C/T]ACACTATGTTAATGG	143279
rs767625098	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460233	AGATACAGCCTAATA[C/T]GTGTTGTGAGTGAAG	143279
rs767632823	snp	G/T	5.52695e-05	0.00525659	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484683	TATTCTATCATTTTT[G/T]ACTTTTCTTTTGTTA	143279
rs767641588	snp	C/G	1.68086e-05	0.00289896	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425335	AGCAGTTTTATTTCA[C/G]CTGTTAGCCCGAAGA	143279
rs767645184	in-del	-/ATTA	1.74421e-05	0.00295309	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491330	TTATTCCAAAATGAT[-/ATTA]ATTAAAGCTTAAAAT	143279
rs767692136	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91510917	ATCCCTGAACAGGTT[A/G]CTTGTATATTTACAT	143279
rs767713143	in-del	-/GCGCAAGCTCCGGGCC			upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409737	CTGTCTCCCCGGGCT[-/GCGCAAGCTCCGGGCC]GCCTCTCCTGGGCTC	143279
rs767731586	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445314	GGTTCAGTAGGAAGA[A/T]CCTGGGCTTCCCTTC	143279
rs767738716	in-del	-/ATAA	1.87686e-05	0.00306332	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500483	TAATTATTGTTTTTG[-/ATAA]ATAAATAATTATTGG	143279
rs767770351	snp	G/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91514021	GCATCCTGGTTTTGT[G/T]TCATTTTGCTCTGTT	143279
rs767772992	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91411716	TTGCGAACAGTAATG[A/T]TACACGTTTAAAAGC	143279
rs767802565	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491973	CCTCAGCCTCCCAAA[G/T]AGTTGGGATTACCAG	143279
rs767817874	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484743	AAAGACTATAGAGGC[A/G]TTCTTAAATTTTAAA	143279
rs767824964	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451498	ACGTTCTGCACATGT[A/G]TTCCAGAACTTAAAG	143279
rs767861029	snp	C/T	0.00252844	0.0354659	utr-variant-5-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410403	GCAACACTGAGGCCG[C/T]CGCCGCCGCCTGGCG	143279
rs767886227	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452514	AGAGGTAATTGAGTC[A/G]TGAGGGCTCTGCTCT	143279
rs767914150	snp	A/G	3.34851e-05	0.00409163	missense, intron-variant, nc-transcript-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481099	TCTTTTTCAGTCCAC[A/G]AACAAAAGATGATCT	143279
rs767933118	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91494052	CTATGATTCCTATCA[G/T]GTATATTGTAGAGGG	143279
rs767954192	snp	A/C/G	0.000313262	0.012512	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496322	AGTGATCAAAATATA[A/C/G]CAGTAGGCATCTGCA	143279
rs768060326	snp	G/T	1.72145e-05	0.00293376	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496188	TCATGGATTTTATGT[G/T]AATGCTTAACATTTA	143279
rs768064086	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91474023	AAGAAAAAGCCAAAA[G/T]ATGGGAGAATAACAA	143279
rs768084447	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91435080	ACATGCAGAAGACTA[A/T]AATCAACATTTTATA	143279
rs768098678	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457175	TTTCTAGTTTTAAAA[C/T]TTTAAAAAAGGAATA	143279
rs768170603	snp	C/T	3.29891e-05	0.00406122	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496266	ATATTCGTTTCCCTC[C/T]CTGCTGTTACAAGAA	143279
rs768197584	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457446	ATAAAATTCAGCAAT[A/T]TGTAAAAAGAGTTAT	143279
rs768201149	snp	A/T	1.71284e-05	0.00292642	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478302	TTAGCTAATCAGTAT[A/T]GATGTCTAACTTACA	143279
rs768242466	snp	C/T	1.93433e-05	0.00310987	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493542	ACTAGGAGGTGCTAA[C/T]AGATTAGAGATTTTT	143279
rs768257502	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467925	GCAAATGCATGTGCA[C/T]AGAGTCCAGCATTCC	143279
rs768271427	in-del	-/AA			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91473699	TAATTGCTTCCACTT[-/AA]TAAACAGTAGATATA	143279
rs768282970	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91424092	TTTCACATAGTCACT[A/C]AAGAACCCAAGCTAA	143279
rs768285355	snp	G/T	1.66454e-05	0.00288486	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501323	CTCAAAGAATGAAAC[G/T]TCTACTAACTGGTAA	143279
rs768358847	in-del	-/TCATGAGGGCTCTGCTCTTTTGAATAGATTAATCCAT			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452512	TAAGAGGTAATTGAG[lengthTooLong]TCATGGGTTAATGGA	143279
rs768400501	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462055	CTAAGAATAGTCTTT[A/C]AAATGTTGAATATAC	143279
rs768443600	snp	A/G	3.30912e-05	0.00406749	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487696	GGTTTTCCTTCTGTC[A/G]GTACCCATTCGTTAT	143279
rs768501744	snp	A/G	1.65293e-05	0.00287479	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512299	GCTTCAATCAACTTT[A/G]CCTTCCCCCCTACAA	143279
rs768514721	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512096	AGTGGTGTCTGATAC[A/G]AAGTGAGGTACTCAG	143279
rs768607998	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450245	AGTAATCTGATCTTT[G/T]ACAAACCTGATAAAA	143279
rs768716066	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91424624	TGATTAATTAAATAA[A/G]TACTATGAATTTTAT	143279
rs768745417	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498239	CATATATGAACAGTG[C/T]AATTTGTTATTAAAT	143279
rs768753300	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91453974	AAAGGGATAATCACC[C/T]AAAATATATAGTCAT	143279
rs768756511	snp	G/T	1.65105e-05	0.00287315	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461305	GAAAGCAGTACATGA[G/T]TTTTATCTAACAACG	143279
rs768852608	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91475457	ATTCCACCTTGTCAG[A/C]TGTTGCTGAGACATT	143279
rs768915045	snp	A/G	1.65457e-05	0.00287621	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484603	AGAATTTCCACCTAT[A/G]ACAAAGTGTTCCTGG	143279
rs768915618	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452441	AGTATTTATTTCCAC[C/G]AAAATTCATGTTGAA	143279
rs768922199	snp	C/T	3.37416e-05	0.00410727	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491314	CTTGATGAGGTATAA[C/T]TTATTCCAAAATGAT	143279
rs768934054	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91413087	GTGTCTATGACTCAA[C/T]TCGTGACCCTACAAT	143279
rs768967166	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483363	TTATTGGTTTTTTAC[A/G]TATCTCAAAGATGGT	143279
rs768978699	snp	A/G			upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409270	AAAAGGAAAAGGAGG[A/G]GGCGACAAGAAAGGA	143279
rs769016843	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91466055	TACCATTAAAGCCAT[C/G]TGGGCCTGGTGCTTT	143279
rs769021978	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91436120	TCTTCTCCCTGCATG[G/T]TGTCTGATTCTTCCA	143279
rs769025012	snp	A/G	1.71393e-05	0.00292734	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484464	TAATTTTGGAAATAG[A/G]AAATGTGAATTTTGA	143279
rs769043221	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420519	AGTAGAACCAGGAGG[C/T]AGAGGTTGCAGTGAG	143279
rs769049817	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467230	AGATTCCATGACCCC[C/G]ATGGACACTTGAGCT	143279
rs769060791	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493097	AAAATTAATTTTGAT[C/G]ATAATTTATAATCTA	143279
rs769076394	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421937	TGTTAACAATTTGGT[C/T]ATTTCTTGGCCCAGG	143279
rs769099709	snp	C/G	1.64936e-05	0.00287168	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499087	TCTGAACAAATCCAT[C/G]TATAAGCAGTTTGCT	143279
rs769121463	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485999	TGCACTTTATATCCA[C/T]ACTTCTAGTTTGGAT	143279
rs769218771	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91436444	TTCTGTTTGTGGGGA[A/G]AAGGAGATTGGGAGT	143279
rs769230775	in-del	-/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433357	TATTCTTTCCTGTGG[-/T]TTTTTTAGGCAAATG	143279
rs769256007	snp	A/G	3.60282e-05	0.00424415	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498867	GTAATGGCATCTCCC[A/G]TCAGGTTTTTCAAGA	143279
rs769287612	in-del	-/T	1.69378e-05	0.00291009	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498974	GGTAAGTTAATACCC[-/T]TTTTAATTAAAATGA	143279
rs769298441	in-del	-/A			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501790	CCTCTTTTTTTTTTT[-/A]ATCTCATGCTTTTTG	143279
rs769331308	snp	A/G	0.000209798	0.0102399	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410492	GCTGGTGGTGGCGGC[A/G]CCCGCGCCTGAGGAG	143279
rs769393811	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422179	TATACTCTGTAGCCT[A/G]AAGGCCTCATAATAT	143279
rs769403074	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444880	TTAGGGTTCATTCAG[C/T]GAACTTATGAACACT	143279
rs769419049	in-del	-/AAATAAATG			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444032	TCAGCAGCAGAAAAT[-/AAATAAATG]AAATAAATGATAGTC	143279
rs769427883	in-del	-/A			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91416182	AGCCAGAGAACCTCC[-/A]AAAAAGTCAAGTACG	143279
rs769429137	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468588	GAAGTAGAATTCAGA[A/C]TATGGATAGGAACAA	143279
rs769432085	in-del	-/C			upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409511	AGAGCAAAACGTAGG[-/C]GCGTGGGGACGGGAA	143279
rs769434012	snp	A/C	5.12142e-05	0.00506009	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491321	AGGTATAATTTATTC[A/C]AAAATGATATTAATT	143279
rs769478460	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91488083	ACCATACCACCAACC[G/T]TAGATAACCAGCAGA	143279
rs769522187	in-del	-/AAGC			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484991	CAAGTTTTCTTTTTT[-/AAGC]AAGAAACTATTGGCT	143279
rs769535448	in-del	-/TTGA			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493703	GAAAGAAATGAGAGT[-/TTGA]TTTTTTTCTGAAAAC	143279
rs769539506	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91475243	AAGCAAAAGTTGATA[A/T]TTGGATTAGCAATTT	143279
rs769546151	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91434426	TGAGTCTTTGACTCA[A/G]CTACTACCTGTAACC	143279
rs769547623	snp	A/C	0.0434568	0.140854	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410607	GGGCCGTCTGGCGCC[A/C]CGGACGGCGGGAGTT	143279
rs769567018	snp	A/C	3.31131e-05	0.00406884	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461338	TGATTCTTTCCCAGA[A/C]TTAAATGCTGCATTT	143279
rs769628474	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91473488	GAAGGATCTGAGATA[C/T]AAGAAAGAATGATGA	143279
rs769639450	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450106	ACAAAGCTGGAGGCA[G/T]CATTGCTACCTCACT	143279
rs769640220	snp	C/T	6.60099e-05	0.00574461	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492369	AACCCGGAAAAGAGC[C/T]GATTTGAAAAAGAAG	143279
rs769728390	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445266	GATGGCAACAGCAGT[A/G]TTGGAGGTAAAGAAG	143279
rs769743195	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91510297	GCAAAGCAAATTTCA[A/G]ATTACATCCTTTTCC	143279
rs769765871	snp	A/G	1.71968e-05	0.00293225	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501351	TAAATTTCTGGATCT[A/G]ATTTTATTTTAAATC	143279
rs769773780	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461037	GCGACATGTTAAGGA[C/T]GATCTTTTTTAAAAA	143279
rs769879171	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91456688	TTCCAGTTTTTGCCC[A/G]TTCAGTATGATATTG	143279
rs769940341	snp	A/G	1.64844e-05	0.00287087	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462107	CAGAAAGATGCCACT[A/G]CCTCATTTAACACCA	143279
rs769955174	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467146	CCAGCAGCTCCTGTG[A/G]AAAGGGTGAGTTGAA	143279
rs769994485	snp	A/G	1.64988e-05	0.00287213	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499127	TATGGATTTCATAGT[A/G]TGTGTGCTTCAAATG	143279
rs770039119	in-del	-/T			intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91515115	CTCCAAAACCATTCA[-/T]TTTGGCCCTTTTCCC	143279
rs770043071	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91465892	GTATTGATCTATACT[C/T]TTCCTTTCTTGTAAT	143279
rs770066075	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433100	AATAACTCCATCTAC[A/G]GGTTTCCTTAAAGAA	143279
rs770114458	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439361	TTGATTGTTTTTGTC[A/G]GATTTGTCAAAGATC	143279
rs770129926	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91479276	TATATCTCAAAGATG[G/T]TGACTGGATTTGCTT	143279
rs770188524	snp	C/T			intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481276	TATAGTTACCTGTAA[C/T]CAGAAGATTTTTTTT	143279
rs770248919	snp	A/C	1.65444e-05	0.00287609	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485281	GAATATCATACTTGG[A/C]AAAACTTTGGAAACT	143279
rs770248946	in-del	-/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91436041	TTTATAGTACCCTTT[-/T]ATTTCATGGTTATAC	143279
rs770252360	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458404	TCAAAATTCCTGTAT[A/G]TTTTTTGTTGTTGAT	143279
rs770259315	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470143	TTCAACACCCCACTG[A/G]CAATATTAGATGATT	143279
rs770275478	in-del	-/AAAAAATACCA	1.65255e-05	0.00287445	frameshift-variant, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512298	GCTTCAATCAACTTT[-/AAAAAATACCA]GCCTTCCCCCCTACA	143279
rs770310558	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91418719	TTTACCCAGGATCAA[A/G]GCCTAAAATAGTCTC	143279
rs770328303	in-del	-/A	6.62394e-05	0.00575459	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498077	AATGCTATTCTATTG[-/A]AAAAAATCATTAACA	143279
rs770379596	in-del	-/AA	1.77423e-05	0.00297839	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491172	AGTCTAAGTAAAAGC[-/AA]AACTGTTTACTTTCT	143279
rs770393620	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412518	GAAGTGCAGTAGCCT[G/T]ATCTCGGCTCACTGC	143279
rs770424343	in-del	-/CA			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500443	CAGTGAAAATAGTTC[-/CA]GTTTCACTTAAAACC	143279
rs770457724	snp	C/T	3.44062e-05	0.00414752	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425236	CAATAAAATAATTTA[C/T]AGGTAGTAGGAAGTA	143279
rs770479514	snp	C/T	0.000249453	0.0111653	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484628	TCCTGGTGGATTCCA[C/T]CAGCCGCTAAAGTGT	143279
rs770493352	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503240	GGTCAGAATGGCTAT[G/T]GTTATATTAAAAAGT	143279
rs770510683	snp	A/C	0.000168734	0.00918359	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410497	TGGTGGCGGCGCCCG[A/C]GCCTGAGGAGAGGAA	143279
rs770522117	in-del	-/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449181	AAGCTCATCTACCAC[-/G]TGAGAGAACTTACCC	143279
rs770522661	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91443806	AGAGAACAATGGTGC[C/T]GATGACACAGAAGAG	143279
rs770522684	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460958	AAGTGGGAATGATAA[A/G]GATAGAATGTAAACA	143279
rs770552200	in-del	-/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439928	ATTTTTGCACACTGA[-/T]TTTTGTATCCTGAGA	143279
rs770588844	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471694	GAGCCAAATCAAGAA[C/T]GCAATTCCACTCACA	143279
rs770601790	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91511749	TCAGGCAGTAATGCT[C/T]GCCTGCCACTCACCT	143279
rs770629559	snp	C/T	3.46969e-05	0.004165	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484380	CAAATGTTTGGCAAT[C/T]TAAGAAATAGAATTT	143279
rs770668804	snp	C/T	1.64827e-05	0.00287073	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462133	CACCATTGAAGACTC[C/T]GGGATTAATGCTAAA	143279
rs770680688	in-del	-/A			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420592	ACTATATCTCAAAAG[-/A]AAAAAAAAAAAAAGA	143279
rs770686977	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451166	GAAAGTATGGCACAT[A/G]TGCACCATGTAATAC	143279
rs770695898	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492846	AGTAACATTTAAAGC[C/G]TCTTTCATTAATGGG	143279
rs770716856	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444748	TAATTAGACCTCAAA[A/C]TGACATTATAAATAG	143279
rs770734724	in-del	-/AC			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426569	TGCATACAAACATAC[-/AC]ACACACACACACACA	143279
rs770770431	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431934	GTGAGGAACTGCGAA[G/T]TTGGGGTATTTGCAT	143279
rs770812902	snp	C/T	1.66732e-05	0.00288727	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493460	ACACTGCCATTGGTT[C/T]AGCAGCTTTAAATGT	143279
rs770859937	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91475673	AGAAGATGGCCCAAA[C/T]GAGATGTTTTAAATA	143279
rs770870960	snp	G/T	1.65124e-05	0.00287331	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500531	AGAGGTTGAAATTTT[G/T]GTCTGTGGAAGTCCT	143279
rs770876597	snp	C/T			upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91408832	GTAAATAGGTGGCAA[C/T]AGCAACTATATTAAA	143279
rs770920532	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91434261	CCACTTGTTATGACT[A/C]ATCCATTCTGGTCTT	143279
rs770924154	snp	A/G	1.65825e-05	0.00287941	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485313	TCACAGGTATGAACA[A/G]AAGTTCCTTTGATTA	143279
rs770925923	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458683	AGTGATTGGACATCT[A/G]TAAACAAAAAATAAT	143279
rs770982427	in-del	-/AT			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438539	AGTGCTGTAATAAAC[-/AT]ATGTGTGTGTGTCTT	143279
rs770990318	snp	A/T			intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91463909	ATGAAGCATATGCAT[A/T]TTCTGTAACCCAACA	143279
rs771011742	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91486811	CAACTTTTATTAACA[A/G]TTTTGTCCCATGGTA	143279
rs771045756	snp	A/C	3.29761e-05	0.00406041	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492421	GAAGCTGGTTTGGAT[A/C]TGGGTGGTTTGACTA	143279
rs771061056	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91465649	ATCATGAATGGGTAT[C/T]GGATTTCATCAACTG	143279
rs771064707	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439179	TGAATGGTATTGCCT[A/G]GGTTTTCTTCTAGGG	143279
rs771090753	snp	A/T	1.74114e-05	0.00295049	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484666	ACTTAGTAGGTTTTT[A/T]TTATTCTATCATTTT	143279
rs771097061	snp	A/G	0.000300591	0.0122558	missense, intron-variant, nc-transcript-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481128	CTTAGAGCATATTTT[A/G]TACTTTTACAGGTAA	143279
rs771101501	snp	A/C			intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482947	AATTTTAACACAATT[A/C]TCTTTAATATCTTTT	143279
rs771198349	in-del	-/TTC	1.66902e-05	0.00288874	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487658	ACACCATTTTGCTTT[-/TTC]TTTTTTTCACTTGTT	143279
rs771231186	snp	C/T	1.65102e-05	0.00287312	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499144	GTGTGCTTCAAATGC[C/T]CTAATGGTGAGTTTA	143279
rs771244607	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457205	ATTCACGTCCGGATG[A/G]TCTCACAAGATAATT	143279
rs771285498	snp	C/G	1.64876e-05	0.00287116	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496290	ACAAGAAATTATTGA[C/G]CCCTCCCATCATTCC	143279
rs771308307	snp	A/G			intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462494	TGAATCTGTAGATCA[A/G]TGGTTCTTAAACATT	143279
rs771350555	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432233	TCATTCTTGGCAGTT[A/C]TTATAATTTTCCTCC	143279
rs771370146	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470237	GATATCTGCAGAACT[C/T]TCCACCCCAAAACAA	143279
rs771398520	in-del	-/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497108	GGGATTTTAGGCATG[-/T]GCCACCGTGCCCGGC	143279
rs771436037	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501027	TTATAATGTTAGTCA[A/G]AAGTCTAATACGTAT	143279
rs771436945	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438197	ATCAACCCGTCATCT[A/G]CATTAAGTATTTCTC	143279
rs771450758	snp	C/T	6.669e-05	0.00577413	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460593	TATTATATGTAAATG[C/T]ATAGTCATCTGCATG	143279
rs771503582	snp	A/T	6.59587e-05	0.00574239	synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460479	AAAACAGCGTACATC[A/T]ATGGATGCATCATCA	143279
rs771546873	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476744	ATGAGGGCAAAGGGC[A/G]AGAGGAGTGAGAACC	143279
rs771558052	snp	A/G	1.877e-05	0.00306344	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425389	TCACCTGCACATCTT[A/G]TTTTCCCTAACATCA	143279
rs771632216	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439710	TGATTCTTCCTATCC[A/G]TGAGGATGGAATGTT	143279
rs771635140	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432649	TTTAAAAGAAATGAA[A/G]CAATTCTTCCCCAAA	143279
rs771641548	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439450	TATATATATATCTGT[A/T]TTGGTACCAGTATCA	143279
rs771656865	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91473200	ATCGTAATAAAGATA[C/T]CTTATAAGTAATCAA	143279
rs771661185	snp	C/G	1.66441e-05	0.00288474	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492498	TGGTAAGTATGTAAT[C/G]TAATTTTTATAAACT	143279
rs771671494	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458661	CCTTTTCAATAAATG[A/G]TGCCAGAGTGATTGG	143279
rs771699624	in-del	-/TTTAA	2.0556e-05	0.00320587	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493547	AGGTGCTAATAGATT[-/TTTAA]AGAGATTTTTAAAGA	143279
rs771746794	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471552	ATGTTATTATTCTAT[A/G]CCTAGAAAACCCCAA	143279
rs771759157	in-del	-/AAATT			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91472312	AAATCAACTCAAGAC[-/AAATT]AAAGACTTTAATGTA	143279
rs771782775	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91513816	CCAACCAGCAGAATT[C/T]TTCCAGGGTGGAGGA	143279
rs771823699	snp	A/G			intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91463708	ACTTCACTATTAAAT[A/G]TAAACATCCTTTGTC	143279
rs771825289	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450513	TGGCAACAAAAGCCA[A/G]AATTGACACATGGCA	143279
rs771904623	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512531	AAAATCAAATATGAA[A/G]TATGTTCAGCAAAGG	143279
rs771915306	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449735	ATCACAAGCATTCCT[A/G]TACACAAATAATAGC	143279
rs771994453	in-del	-/ACAT			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509497	TTCTGTCATAAAGAC[-/ACAT]GCATGCATATGTTCA	143279
rs772007424	snp	C/T	1.78052e-05	0.00298367	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487630	ATTCCCTTAGTATAA[C/T]TTTGTTAAAAATACA	143279
rs772024766	snp	A/G	1.70574e-05	0.00292035	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478297	AATATTTAGCTAATC[A/G]GTATAGATGTCTAAC	143279
rs772030060	snp	C/G	1.68479e-05	0.00290236	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460612	GTCATCTGCATGTCA[C/G]CACTTTACATAATTT	143279
rs772032504	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490077	TATTTTGAAAAACGG[C/T]GACAAAAGAATTTTG	143279
rs772060493	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91453045	AAATACAATAGACTT[C/T]TCTTCTCCTCTTATG	143279
rs772070638	in-del	-/A			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91486625	CAGTGTATCATTCAC[-/A]AAGTATCATTTCTCT	143279
rs772111960	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91436368	ATTTCTTCTTAGCCT[A/C]ATCAGATTCCCCACG	143279
rs772139627	in-del	-/AA			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471023	ACACGCACACACACA[-/AA]GAAAACCTCAGGCCA	143279
rs772160976	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425609	TGAAATACAAAACTC[A/G]TGAATAATAAGCAAA	143279
rs772193451	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478429	TTACAACAAAGCTGT[A/G]TAACTTGAGATTTGT	143279
rs772249317	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457106	AAAACAAAAGCTATT[A/G]CAGCTCATCCAGTTT	143279
rs772281026	snp	A/G	1.65012e-05	0.00287234	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500575	ATGCTCTGCAGAGAA[A/G]TACTCAGTATGATGG	143279
rs772306975	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432128	ATAGAAAGTTAGGCT[A/G]CATCTTCCAAATGTA	143279
rs772323511	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498486	CTGTAACTTCAACAT[G/T]AGAAGCTAGGAGTAG	143279
rs772328692	snp	C/T	1.88891e-05	0.00307314	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498849	TCAACCATATTAATA[C/T]GTGTAATGGCATCTC	143279
rs772329984	snp	A/G	1.64966e-05	0.00287194	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501270	ACAGGGAGTGACAGA[A/G]TACCTGTAGGAGGGA	143279
rs772345467	snp	C/T			intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462416	TTTAGAAAGACTTGC[C/T]AAAATCATGCTTTAC	143279
rs772387348	snp	A/T	1.66305e-05	0.00288357	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485332	TTCCTTTGATTATCC[A/T]CCTAAATGAAATACT	143279
rs772433684	snp	A/G	3.3355e-05	0.00408367	missense, intron-variant, nc-transcript-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483027	TTGCTACGACAGATA[A/G]CTACCTTAGTGGAAG	143279
rs772437292	snp	C/T	1.65723e-05	0.00287852	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498062	CTTCATTATCCTAGC[C/T]AATGCTATTCTATTG	143279
rs772444693	in-del	-/TATC			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425164	ATTTATATACGTTTT[-/TATC]TATTATCTACTCGTC	143279
rs772462398	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485877	AGTGGTTGTCCATTA[A/G]GTGCAATATAAAAAG	143279
rs772472762	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91454199	GCACATTTACAGCAC[A/G]CTCTACTCAACAACA	143279
rs772478043	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467327	TGGTATGGGAACATC[C/T]GCAGTGGAGCATGGC	143279
rs772489352	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461931	AAGTTATTAAAATAA[G/T]CTTTGTACATTTCTT	143279
rs772495943	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496982	TTTTTTTTTTTGAGA[C/G]AGAATCTCACTCTGT	143279
rs772563626	snp	A/G	1.65083e-05	0.00287296	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461293	ATCAGGAGATTGGAA[A/G]GCAGTACATGATTTT	143279
rs772564373	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491489	AGTTAAAATCAGATC[C/T]GTATTCATAATTGTC	143279
rs772577304	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91459607	TCATATAACATTCTT[G/T]AAATGACAACATTTT	143279
rs772679052	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439832	GCTAGGTATTTTATT[A/C]TCTTTGTAGCAGTTA	143279
rs772694740	snp	C/G			missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501200	CTCTAGATACTTTTG[C/G]GATGTTGTGCTTGGA	143279
rs772766977	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91475125	TCATTGAGTGTTTTC[A/G]GCAGGGATCATTTAT	143279
rs772785778	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91459580	GAAAAGGTTACATAG[G/T]TGTGATTTCTTTCAT	143279
rs772873773	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458756	AAAATGGATAATGGA[C/T]TTAAATGTTAAATTA	143279
rs772877003	snp	A/G	1.66907e-05	0.00288879	missense, intron-variant, nc-transcript-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483004	CTACGTATGTCATCT[A/G]TGCTCACTTGCTACG	143279
rs772878639	snp	A/T	1.7154e-05	0.0029286	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481052	TAGATGCTATGAGAT[A/T]AAACATTCATCCATA	143279
rs772906775	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419100	AGCACTTACTCCTTT[G/T]TTCAAGGATTGGGTT	143279
rs772911089	snp	G/T	1.73354e-05	0.00294404	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501358	CTGGATCTAATTTTA[G/T]TTTAAATCTAAAGGT	143279
rs772989121	snp	A/G	1.65649e-05	0.00287788	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487744	AAATCATTATTCAGA[A/G]AGACTCAGAGCAACA	143279
rs773024796	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91424392	AGGAGGAGATGAAAA[A/G]GAAACTCTTCCTCTA	143279
rs773025068	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450549	TTAAACTAAAGAGCT[C/T]CTAAACAGTAAAAGA	143279
rs773105859	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415673	AACACTCGACATTTG[C/T]GGTCATAGGTAATAG	143279
rs773128987	snp	C/T	1.68007e-05	0.00289828	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461368	TAAGGTAATTATACA[C/T]AAAACACACTTTTCA	143279
rs773167045	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476586	GCAGGATATGGCGCA[A/G]TGCCACCACCGCAGG	143279
rs773254454	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457595	CAAAATCCAACACCT[A/G]TTCATAATGAAAAAA	143279
rs773324955	snp	C/T	1.6483e-05	0.00287076	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462121	TGCCTCATTTAACAC[C/T]ATTGAAGACTCTGGG	143279
rs773384187	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91435154	AGCACTACTGGCACT[A/G]TAAAAGCCCCAGGGA	143279
rs773403690	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449741	AGCATTCCTATACAC[A/G]AATAATAGCCAAATC	143279
rs773466307	snp	A/G			intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91463849	ATGATGTAAGTATAA[A/G]TTGGTACAACCACTT	143279
rs773490107	snp	A/C	1.68821e-05	0.0029053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484498	CAATTATTTTGAAAT[A/C]TTTACCAGATTGTCC	143279
rs773606622	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426491	CTATTCTACATTCTT[A/G]TAGGTTAGTATTTTT	143279
rs773717807	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91475627	TGAGAGCTTTCACTA[C/T]GAAGGGAAGCAGAGA	143279
rs773774144	snp	A/G	8.24491e-05	0.0064201	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460474	AGACAAAAACAGCGT[A/G]CATCTATGGATGCAT	143279
rs773787593	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493594	GAAAACTGTTTTCTT[C/T]AGCCATTTTATCCAA	143279
rs773802659	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498662	TTTAACTGTATTAGG[C/T]AGGGTTAAGTTAAGG	143279
rs773809631	in-del	-/AG			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471024	CACGCACACACACAA[-/AG]AAAACCTCAGGCCAA	143279
rs773829470	snp	A/G	1.66098e-05	0.00288177	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484634	TGGATTCCATCAGCC[A/G]CTAAAGTGTTGGCTT	143279
rs773832532	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91454205	TTACAGCACGCTCTA[C/G]TCAACAACAGAATAC	143279
rs773837070	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91436667	GGCAAGGAAGAGATC[G/T]AGGGAGCTAACTTTT	143279
rs773842872	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91435958	CTCAAAACTCTTCTA[C/T]TGAGTATCTTACTTC	143279
rs773852550	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458631	TCCAAAAGCAATTCA[A/G]TGAAGGAAAAATAAC	143279
rs773856552	in-del	-/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437620	GTTGGATGGTTGTTC[-/T]TTTTTTTTTTTTTTT	143279
rs773901220	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509393	TTAGCCATTGTGGAA[A/G]GCAGTATGGAGGTTT	143279
rs773959658	snp	G/T	1.71997e-05	0.0029325	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425239	TAAAATAATTTATAG[G/T]TAGTAGGAAGTATAC	143279
rs773970050	in-del	-/AAAAG	1.92944e-05	0.00310593	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487527	ATGGCTGTGAGAATT[-/AAAAG]AAATTATACACATAC	143279
rs773971873	snp	C/T	0.000104641	0.00723253	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484388	TGGCAATTTAAGAAA[C/T]AGAATTTGGGGGAAT	143279
rs774002542	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470605	ATGTTAGATCTCAAG[G/T]AAACATAATATCACA	143279
rs774014090	snp	A/T	2.08914e-05	0.00323192	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410503	CGGCGCCCGCGCCTG[A/T]GGAGAGGAAAGGGAA	143279
rs774016398	in-del	-/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467942	AGTCCAGCATTCCTG[-/C]CCCCCCACCAGCACC	143279
rs774065558	snp	A/G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449727	GTGCAAAAATCACAA[A/G/T]CATTCCTATACACAA	143279
rs774067778	snp	A/C	4.03739e-05	0.00449281	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491346	TTAATTAAAGCTTAA[A/C]ATTCTATAATATGAT	143279
rs774075968	in-del	-/A			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91480965	GACTGTCTCAATAAT[-/A]ATGCATATTAATCCT	143279
rs774079201	snp	C/G	1.68525e-05	0.00290275	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478154	AACATATAAACGTCA[C/G]CTAATTTGGTAATCC	143279
rs774121434	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457490	AAGGTCACTCCAGGG[A/T]TGCTAGATGGTTCAG	143279
rs774131769	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422505	GCACTATTATTAAGA[G/T]TTTCTGACAACAAAA	143279
rs774146518	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91424186	CTAGAGTTTTGCCCC[A/C]GTCTTAAATGCATTG	143279
rs774155400	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445032	GTGGTAGGGGTTGGC[A/G]GTATATTCAAAAATG	143279
rs774155548	snp	A/G	1.65135e-05	0.00287341	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462082	ATACTTAATTCTTAA[A/G]TTGAATTTGCAGAAA	143279
rs774197749	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91513686	GAAAACTCTGAAGTT[A/G]TATTTGCAATAATAA	143279
rs774306140	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91495433	CCAATTTTTAAAAGT[C/T]ATTTTCAGTAATTTA	143279
rs774321238	snp	C/T	1.64827e-05	0.00287073	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462142	AGACTCTGGGATTAA[C/T]GCTAAATTTGTGAAT	143279
rs774353142	snp	C/G			upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410138	GCCCTCGGGGTTGAC[C/G]AGGGGGACTACCGCC	143279
rs774381143	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91488541	TGCTCACAATTTTAA[A/G]AGAGGGAAGCTTGGC	143279
rs774399944	snp	A/G	1.65225e-05	0.00287419	splice-donor-variant, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499151	TCAAATGCCCTAATG[A/G]TGAGTTTATAACTTT	143279
rs774403501	snp	A/G	1.65111e-05	0.0028732	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492465	TCTTCTAATTCGCCA[A/G]ATTTTTCATCCAGAT	143279
rs774429824	in-del	-/G	1.68315e-05	0.00290094	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498994	AATTAAAATGAATTA[-/G]TATTTGCCATTTACT	143279
rs774502958	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91473735	CTCGTGATTTTCTTA[A/G]TAACATTATCTTTTC	143279
rs774503245	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91475517	TGTCTTTCATAAGCT[A/G]TAGATAATTGATGAC	143279
rs774504422	in-del	-/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485966	TTTGTAAAACAGTCA[-/C]CAAATTATTTAATAC	143279
rs774516044	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91436239	GTTAATGAGGGAACC[A/G]AGATGGATGATTGGA	143279
rs774560079	snp	A/G	1.65866e-05	0.00287976	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485316	CAGGTATGAACAAAA[A/G]TTCCTTTGATTATCC	143279
rs774576151	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420968	GGCAATTTAAATATA[A/G]GGGAACATTAGATGG	143279
rs774593502	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91466176	TAGATTGTGTTTTTC[A/T]GTAACATATCTAGGT	143279
rs774639619	in-del	-/TA			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412855	CTAGGAAGGCCTTGG[-/TA]TATGTGTGGGGAGGG	143279
rs774649871	snp	A/G	1.64961e-05	0.00287189	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500569	ATATGCATGCTCTGC[A/G]GAGAAGTACTCAGTA	143279
rs774666505	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91459490	GGAATACTATTAAGC[A/T]ATAAAAATGAACTAT	143279
rs774759998	snp	C/T	1.64855e-05	0.00287097	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496294	GAAATTATTGAGCCC[C/T]CCCATCATTCCTAGT	143279
rs774837087	in-del	-/TTT			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493134	ATACTTTTTATAAAG[-/TTT]TTATCTGATTCATTT	143279
rs774883095	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493821	AAAGTATTTCCCATT[C/T]ATAATGAAGTATTTT	143279
rs774926911	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491404	TATTTCTGTATGCCA[A/G]TAAGTGTGCTTCCTT	143279
rs774930650	snp	C/T	1.79506e-05	0.00299583	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493523	TGTATCCTTTAAACT[C/T]TCCACTAGGAGGTGC	143279
rs774985584	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470279	TTCTTCTGAACTGTA[C/T]ATGACACATACTTTA	143279
rs775063878	in-del	-/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410650	GCCGGGCGAGGGCCG[-/T]TCAGGAGGCCTGCGT	143279
rs775073895	snp	A/T	1.64982e-05	0.00287208	intron-variant, missense	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462195	ATACTGTAAGTATTA[A/T]GACATGCAAGTAATA	143279
rs775081497	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91486260	CTCAGAACTGAATAA[A/G]AATAAGAATTTAAGT	143279
rs775086142	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91423928	AATGATTGGTTTTAT[A/G]GAAATGGTGAACACT	143279
rs775138194	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497434	TAGCTGGGATTACAG[A/G]TGTGAGCCACCACAC	143279
rs775168326	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422183	CTCTGTAGCCTGAAG[G/T]CCTCATAATATGGCC	143279
rs775222235	snp	C/T	1.66877e-05	0.00288852	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492508	GTAATCTAATTTTTA[C/T]AAACTGTGTTTCTTC	143279
rs775266307	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444912	TGCTGAACTGATAAG[C/G]AGTAATCGTTTTCCC	143279
rs775267993	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468593	AGAATTCAGAATATG[G/T]ATAGGAACAAAGATC	143279
rs775269289	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91475406	ATGGATAAGGCATTC[A/G]TGAAGGAGAGATCAA	143279
rs775322620	snp	A/G	1.65113e-05	0.00287322	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500586	AGAAGTACTCAGTAT[A/G]ATGGCTATGCAAAAA	143279
rs775367885	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460084	AAAAACATTGAGCCT[C/T]ATTGAAATACCCCCG	143279
rs775414432	snp	A/T	1.66051e-05	0.00288137	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499176	AACTTTAAATCAAGC[A/T]TTCGGTTAGCTTTTG	143279
rs775503663	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445390	TGCTGCTGGTTACAC[A/G]CTCTTGCAAAATGCT	143279
rs775532513	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512023	ATGCTTCTTAAATGA[A/G]TTTCATGAAAGTGGT	143279
rs775538959	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491759	TTTGATTGCATTTTC[A/G]TGTATTATCATAAAA	143279
rs775558429	snp	A/T			upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409136	ATAATGAAGGCACAG[A/T]TAAAAAATCTGATAG	143279
rs775564182	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444196	ACCTACAATTAAATA[C/T]AAACAGATTCATTCA	143279
rs775591511	snp	C/T	1.67008e-05	0.00288965	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478176	TGGTAATCCTAATTA[C/T]CTTACTGTTTTCTTT	143279
rs775646890	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452201	AAGGAGAGGAAAAGA[C/T]AGTAGGGCTAAAAAA	143279
rs775679783	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91510765	CTTTGTTATTTGATG[A/G]TATTTTTAATTCATA	143279
rs775689151	in-del	-/ACAT			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487172	ATAATACTAAATGTA[-/ACAT]ACATTTCTGATTTAT	143279
rs775705343	snp	A/T	1.67013e-05	0.0028897	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461209	TACTAGTTTATCTGA[A/T]TAATATTTCTATATG	143279
rs775712851	snp	C/T	5.18766e-05	0.0050927	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487636	TTAGTATAATTTTGT[C/T]AAAAATACACCATTT	143279
rs775719405	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91456742	TCTTATTATTTTGAG[A/G]TACGTCAAAAAGGGG	143279
rs775729453	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493120	ATAATCTATGAAACT[A/C]TACTTTTTATAAAGT	143279
rs775732878	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451240	CATGGACGAAGCTGG[A/G]AAGCATTATTCTCAG	143279
rs775778338	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91418765	TTATATCGTTGGCTC[C/G]AGGATGGCTCTGATT	143279
rs775805197	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490618	GAGACATGGCCGGGC[A/G]CGGTGGCTCACGCCT	143279
rs775868086	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415941	GGCTATGGCTTTATA[A/T]ATACATACCCAGCAT	143279
rs775877619	snp	C/T	1.65636e-05	0.00287776	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498070	TCCTAGCTAATGCTA[C/T]TCTATTGAAAAAATC	143279
rs775902740	snp	C/T	1.66835e-05	0.00288816	synonymous-codon, intron-variant, nc-transcript-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483032	ACGACAGATAGCTAC[C/T]TTAGTGGAAGCTGAC	143279
rs776071586	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91494331	ATTTAAAAAATGGAA[A/C]AATTACATTTGATTA	143279
rs776073775	snp	A/T	1.7227e-05	0.00293482	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478307	TAATCAGTATAGATG[A/T]CTAACTTACACATCA	143279
rs776097866	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432405	TCACATGACTAGGTA[A/T]GCCTGTCAAATTGAC	143279
rs776123156	in-del	-/AA	4.95307e-05	0.00497623	splice-acceptor-variant, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498105	CAGATTTCTTTTTAT[-/AA]AGGAGTTGGCCCATG	143279
rs776167578	snp	A/G	3.2969e-05	0.00405998	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496282	CTGCTGTTACAAGAA[A/G]TTATTGAGCCCTCCC	143279
rs776178157	in-del	-/ATTTCATTTAAAAC	1.68707e-05	0.00290432	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491312	ACTTGATGAGGTATA[-/ATTTCATTTAAAAC]ATTTATTCCAAAATG	143279
rs776209700	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444839	TGAAAAAAGCCAAAA[C/T]ATATTTATCAGTGAA	143279
rs776216122	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91510151	TAGAATAAAGTCCAT[A/G]GAGAAAATAATCTTC	143279
rs776220575	in-del	-/AGA			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432626	ATTTTTAAGTAGCAC[-/AGA]ATATCTTTAAAAGAA	143279
rs776239188	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467358	CAGGGTTGCCCATCC[C/G]TCAAGGCTCACTGTG	143279
rs776314345	snp	C/G	3.96024e-05	0.00444968	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493544	TAGGAGGTGCTAATA[C/G]ATTAGAGATTTTTAA	143279
rs776326489	snp	C/G	1.65594e-05	0.0028774	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478195	ACTGTTTTCTTTTGC[C/G]TACAGCCTCAAGACG	143279
rs776328960	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483557	TTTTTTCACAGAACT[A/G]TACCCACATGAACAA	143279
rs776477108	snp	C/T	3.30764e-05	0.00406659	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487706	CTGTCAGTACCCATT[C/T]GTTATTTCTGTAGCT	143279
rs776516619	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432910	ATCGCAATTGGATCT[A/G]TGTGTGAGTCCTGTG	143279
rs776547956	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478353	TGTGTATGTATTTTA[C/T]TCTCAGAAAAGATTT	143279
rs776589722	in-del	-/AAGTA			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499400	TTACAAACTTTCTCC[-/AAGTA]GAGTGGATGAAGGGA	143279
rs776677353	snp	A/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91514486	CTGTTACATTTTATT[A/T]ATTTAAAAAGCTAGA	143279
rs776684850	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458795	TTAGAAAAAAAATGA[A/G]ACGATCTTTGGGCTC	143279
rs776695864	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432157	TAAGCATGTTTATAG[C/T]TTCTTGATGTTTTGG	143279
rs776780063	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450653	CTAATATCCAGAATC[C/T]ACAAGGAAGTTAAAC	143279
rs776781532	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491523	TATTCATGTTTGTAT[A/G]TTTATTAATAGTTTG	143279
rs776810107	snp	A/C/T	0.000136309	0.0082546	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491320	GAGGTATAATTTATT[A/C/T]CAAAATGATATTAAT	143279
rs776849599	snp	A/C/T	9.67341e-05	0.00695405	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498824	CTGTTCACCAAAGTA[A/C/T]GTTATTATATCAACC	143279
rs776860744	snp	C/G			intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464049	ATCTAGTCCTCGAGG[C/G]ATCCAGGCTGAGTCT	143279
rs776861399	in-del	-/AGAT			frameshift-variant, intron-variant, nc-transcript-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483022	CTCACTTGCTACGAC[-/AGAT]AGCTACCTTAGTGGA	143279
rs776889727	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451167	AAAGTATGGCACATA[C/T]GCACCATGTAATACT	143279
rs776909830	snp	A/T	1.65211e-05	0.00287407	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498096	AAATCATTAACAGAT[A/T]TCTTTTTATAGGAGT	143279
rs776927620	snp	C/T	3.37211e-05	0.00410602	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425272	CAATGTTAACTTTTC[C/T]GTTTTCAGGGTTTGG	143279
rs776989954	in-del	-/TTG	1.66026e-05	0.00288115	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487671	TTTTCTTTTTTTCAC[-/TTG]TTGAGCAGGTTTTCC	143279
rs776991042	in-del	-/G	7.13343e-05	0.00597177	utr-variant-5-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410402	AGCAACACTGAGGCC[-/G]CCGCCGCCGCCTGGC	143279
rs776998471	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437033	TTGTTTCTTTAACAG[A/T]TAAGGAGTATGAGAT	143279
rs777025800	snp	C/T	1.71281e-05	0.00292639	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484470	TGGAAATAGAAAATG[C/T]GAATTTTGATTGCAA	143279
rs777165519	snp	C/T	6.69826e-05	0.00578678	synonymous-codon, intron-variant, nc-transcript-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483050	AGTGGAAGCTGACCA[C/T]CATTTCCTAGTTCAC	143279
rs777200953	snp	A/G	0.000175855	0.00937532	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484330	TATTTCTCATTTAAC[A/G]AAGACAGTATTCAAG	143279
rs777201101	snp	C/T	1.66729e-05	0.00288724	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499017	CATTTACTTTTACTA[C/T]TTAAGAGATGTAAAA	143279
rs777232373	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478654	TTCTATTATAGGGAC[A/G]CCTAAGGCCAGCTAC	143279
rs777244927	snp	C/G	1.78915e-05	0.00299089	splice-acceptor-variant, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498871	TGGCATCTCCCATCA[C/G]GTTTTTCAAGAAGAA	143279
rs777305080	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91434124	TTTATTTGGCTCTGA[C/T]GGCTAAAGTCCTGTG	143279
rs777317735	in-del	-/ATTTTTAA	2.05008e-05	0.00320156	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493549	GTGCTAATAGATTAG[-/ATTTTTAA]AGATTTTTAAAGATT	143279
rs777329058	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444570	CAAACTACAGGATGC[A/G]ACATTCAGCTATTAA	143279
rs777356172	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91510083	AATAAGCCAGTGCAG[G/T]ATTTCAATTTTAAAT	143279
rs777360958	snp	A/G	1.65012e-05	0.00287234	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492370	ACCCGGAAAAGAGCC[A/G]ATTTGAAAAAGAAGT	143279
rs777394794	in-del	-/GT			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415195	CAAATTAGAGAAAGT[-/GT]GTGTGTGTGTGTGTG	143279
rs777395878	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91411122	ATGGTTTTATTTTTC[A/G]TATGGTACAGACATG	143279
rs777403907	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412294	ACACTTCAGTTTCAA[G/T]AATTTATAGGACTTT	143279
rs777430690	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420182	GATTAATTTCATGTC[A/C]TCTCAAGTATAACGT	143279
rs777448142	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91465461	AAAAGAACCACAGCT[C/T]CCTAGAGAAATGGCT	143279
rs777456737	in-del	-/T	1.6681e-05	0.00288794	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512250	AGTATTTTTTTTTAA[-/T]TTTTTTTCCCTAGCT	143279
rs777476169	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451126	GGAACCAACCCAAAT[A/G]CCCGTCAATGATAGA	143279
rs777546059	in-del	-/A			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91494675	AAAGTGCTAAATTCC[-/A]CAAAATGAATAACGC	143279
rs777633461	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458400	CCTGTCAAAATTCCT[G/T]TATGTTTTTTGTTGT	143279
rs777676545	snp	A/C	3.3106e-05	0.0040684	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484556	AGATTGCTGCAATTT[A/C]TTTCTTTACGCCTGT	143279
rs777741222	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492725	AAAAGTAAACATTTA[A/T]GAGGAAACATCCATA	143279
rs777744189	in-del	-/A			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497973	ATGGTAGAAATCATT[-/A]ACCATTTTGTGCCCT	143279
rs777744786	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438146	GTGCAAGTTTGTTTC[A/G]TAGGTATACACGTGC	143279
rs777771105	snp	A/G	1.65636e-05	0.00287776	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478253	TTAACAGCCTGTTAC[A/G]AGAATGGAAAGGGTA	143279
rs777847290	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438993	CCCTTTGTCAGATGG[A/C]TAGATTGCAAACATT	143279
rs777852861	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439922	GCTTGTGATTTTTGC[A/G]CACTGATTTTGTATC	143279
rs778021941	snp	C/G	0.00039968	0.0141308	intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462240	TTCTGTATATCAAAA[C/G]CAGCCATACAAATAT	143279
rs778038338	snp	A/T	5.08488e-05	0.005042	splice-acceptor-variant, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493418	TTCGTGTGTTTTTTT[A/T]GGCATGTTTACATAT	143279
rs778048647	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91417152	TTTTCTCCTTTTTTT[A/G]TAGTTTTGTAGTTAA	143279
rs778070585	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497054	AACCTCCGCCTCCTG[A/G]GTTCAAGTGATTCTC	143279
rs778111898	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478459	TGACCTCTCAGTAGG[A/C]TCTATAGATGGGCAT	143279
rs778176086	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91466283	ATGATCTTTCATTTA[C/G]TAATTAGTATTTTCT	143279
rs778185845	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500933	TATGTTGAAAAATAA[C/G]ACTTGAAAGTTATGC	143279
rs778205511	snp	C/T			intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91489373	ACAAGGACAATCTTA[C/T]AAATAGTCAGTGTAA	143279
rs778210520	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502146	TTCCGTGGGAAATAA[A/C]TTTATTGCCAGTTTA	143279
rs778220903	snp	A/G	5.68715e-05	0.00533221	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487599	ATGTTTTATATTGCT[A/G]CAAGGGGTACCTTAG	143279
rs778227283	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457140	ATAGTTAATTTGCCT[C/T]GTTTTATAACCACTA	143279
rs778230406	in-del	-/ACAC			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470974	TTCTGTGTGGCAGAG[-/ACAC]ACACACACACACGCA	143279
rs778315505	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91469847	CACATACAGTGACAT[C/G]CATAGGCTCAAAGTA	143279
rs778369551	snp	C/T	1.64982e-05	0.00287208	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501186	TTTCCTTTGGTATTC[C/T]CTAGATACTTTTGGG	143279
rs778409807	snp	A/T	1.65353e-05	0.00287531	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499044	AAAATTGCTTTTCAG[A/T]ATATGTACAGCTTTA	143279
rs778428769	snp	A/C	1.67899e-05	0.00289736	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485170	TTTATGTTAGAATTT[A/C]TCTTTACAGATACTG	143279
rs778438194	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91446574	AATAAGAAACTCTTC[C/T]GAGCTAAAGGAGCAC	143279
rs778451899	snp	C/T	1.65553e-05	0.00287705	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485296	CAAAACTTTGGAAAC[C/T]CTCACAGGTATGAAC	143279
rs778452264	snp	C/T	1.79287e-05	0.002994	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425378	AAAACAGAAGTTCAC[C/T]TGCACATCTTGTTTT	143279
rs778461214	snp	A/G	1.65378e-05	0.00287552	synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484579	ACGCCTGTTTCCTGC[A/G]AAGCCTGAAGAATTT	143279
rs778477265	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415867	GATCATTAAATTATA[A/T]GTAAAATCAATCTGA	143279
rs778565141	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91455492	TTGTCAGATGAGTAG[A/T]TTGCAAAAATGTTCT	143279
rs778601867	snp	C/T			synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478242	AAAGGGAATCATTAA[C/T]AGCCTGTTACGAGAA	143279
rs778615697	snp	C/T			intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91463453	CACAATTCAAGCCTG[C/T]ATTCAAGAGTCAACT	143279
rs778633454	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433855	TGAATGGGAGGCACT[G/T]TTTCTGGGTTTCTGG	143279
rs778672081	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457967	AAAAAAGACATACAG[A/G]TTAGAAAATAAGAAA	143279
rs778766362	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492289	ACATTTCCCAGAATT[A/G]AAAATGTTAATTCTC	143279
rs778783179	snp	C/T	1.65776e-05	0.00287898	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496234	GGGACTAGCTGTTTA[C/T]AACAGCATCACCTTG	143279
rs778801098	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91417033	GTGTTTGGAAATTAA[C/G]TATTTTTAGTTAAAG	143279
rs778812209	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450440	GAAGAAAACCTAGGC[A/C]GTACCATTCAGGACA	143279
rs778812251	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464914	GGAAAAAACCCTAAA[C/T]GGAACCTAAAATGGA	143279
rs778838439	in-del	-/TT	1.67133e-05	0.00289074	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512233	TGTGTGTTTCAAGAC[-/TT]TTAGTATTTTTTTTT	143279
rs778853704	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91424971	TAACATTAATGGAGG[G/T]TGTATAATGTGCAAG	143279
rs778901539	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415499	ATGCAACCAAAAGCA[A/G]TCACAACAACCCTGT	143279
rs778908428	snp	G/T	0.000101932	0.00713831	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410485	CCACTCCGCTGGTGG[G/T]GGCGGCGCCCGCGCC	143279
rs778930988	snp	A/G	1.64917e-05	0.00287151	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501245	TCAAAAGAAGTTGCT[A/G]CATTTTACTACAGGG	143279
rs778976260	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500075	CGGTAGACTAACCCA[C/T]CTGAAAGTTGAAAAA	143279
rs779018024	snp	C/T	1.70382e-05	0.0029187	stop-gained, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493494	AACTATTCTGAATTC[C/T]GATTGGTTGGAATTG	143279
rs779165047	in-del	-/A			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91424945	TTTAAATACACAGTT[-/A]AAATTGTAGTTAACA	143279
rs779200678	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464654	TATTTCTCTTTACTA[C/T]TGGGGATTCTGGTAG	143279
rs779208551	snp	C/T	1.69215e-05	0.00290869	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478284	AACTAATATTTTCAA[C/T]ATTTAGCTAATCAGT	143279
rs779218164	in-del	-/AT			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461459	TTGATTTAAACATGC[-/AT]ATATTATGTATTGAT	143279
rs779236792	snp	C/T	0.000217506	0.0104262	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481160	AGAACCAGAACCTAG[C/T]TGAAGTTGTCTAAGT	143279
rs779250072	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91511451	TCCTCGGCTGCTAGA[C/T]GTTTTGTGTATATCA	143279
rs779261778	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498378	GTGCTTAATGAAATT[A/C]ACTAAGGGTTCAGAG	143279
rs779268779	snp	A/T	2.16106e-05	0.00328707	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487612	CTACAAGGGGTACCT[A/T]AGATTCCCTTAGTAT	143279
rs779342105	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444022	AAAAGGGCATCTCAG[C/T]AGCAGAAAATAAATA	143279
rs779375337	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450342	GAAAACTGAAACTGG[A/C]CCCCTTCCTTACACC	143279
rs779435655	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439534	TGTCTCCAGCTTTGT[G/T]CTTTTTGCTTAGGAT	143279
rs779448107	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461598	CTGTTGCCCAGGCTA[C/G]AATGCAGTGGTGCAG	143279
rs779451895	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485796	GGTTTGCAGATGCAT[G/T]ATCTAATATATTGAT	143279
rs779476888	snp	C/T	1.65078e-05	0.00287291	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461287	TAAGTCATCAGGAGA[C/T]TGGAAAGCAGTACAT	143279
rs779508063	snp	A/G	1.66538e-05	0.00288559	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491220	TCTGGTGGATAAAGT[A/G]TCTCGAAGACAGAGA	143279
rs779528097	snp	C/T	1.67567e-05	0.00289449	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460605	ATGTATAGTCATCTG[C/T]ATGTCAGCACTTTAC	143279
rs779535332	snp	A/G	1.64925e-05	0.00287158	synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460470	TGTTAGACAAAAACA[A/G]CGTACATCTATGGAT	143279
rs779557677	snp	A/T	1.65427e-05	0.00287595	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485219	CTCCCCTTATTCCTT[A/T]TACTGATTTCTATAA	143279
rs779639630	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91488113	AGCATTGAGAACTGC[A/G]GTGAGGCAGAGTGTC	143279
rs779703079	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484997	TTCTTTTTTAAGCAA[A/G]AAACTATTGGCTGCA	143279
rs779718374	in-del	-/TATC			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91480044	TATTATATTTTCCTA[-/TATC]TATCTCACGTTTCAG	143279
rs779728661	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91513534	TTTCTAATAAAGTAG[C/T]ATGTAAAAAGAAACT	143279
rs779792832	snp	A/G	0.000268276	0.0115787	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487556	ACATACAATCATTTT[A/G]TATATGGTAAAACAC	143279
rs779851358	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426378	GAAATATTTAAGGAC[A/G]TAGTTTCTGGTAAAT	143279
rs779887188	snp	A/C	1.72392e-05	0.00293586	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496395	TAAAGTTATTAATAT[A/C]TTGTCCTTTAATGCG	143279
rs779894198	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452286	AGATTCAAGAAGCTA[A/C]ACAAACCTCATTCAG	143279
rs779936786	in-del	-/ATG	2.37922e-05	0.00344899	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491357	TTAAAATTCTATAAT[-/ATG]ATTATTATAAAAATC	143279
rs779945669	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437734	TTTTATAATAGATGA[C/T]ATATACATTGTAAGT	143279
rs779976487	snp	G/T			intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481981	GAAAATGACCAAGAG[G/T]TAGTTAAGAAGAGAA	143279
rs779988034	in-del	-/TT	1.8941e-05	0.00307736	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484361	GTAAGATTTTGTATC[-/TT]TTCAAATGTTTGGCA	143279
rs780017753	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461968	TTCAGAAATTTTGCC[C/G]TAACAGTTCTTTTTT	143279
rs780017761	snp	C/T	1.65067e-05	0.00287282	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496256	ATCACCTTGGATATT[C/T]GTTTCCCTCCCTGCT	143279
rs780020126	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467190	GCCTGCTCTTGCCAC[A/G]GGCCTCCGGAATCCT	143279
rs780039338	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91435959	TCAAAACTCTTCTAT[C/T]GAGTATCTTACTTCT	143279
rs780041127	snp	G/T	1.66327e-05	0.00288376	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491289	ACGGACACATCTGGT[G/T]AGCGATTCACTTGAT	143279
rs780046282	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415035	TGAGGCAATGAGTGC[A/G]TCCACTAAGGTGGTG	143279
rs780109529	snp	A/T	1.71261e-05	0.00292622	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478299	TATTTAGCTAATCAG[A/T]ATAGATGTCTAACTT	143279
rs780116507	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468274	CCCCAGAGTTAGAGC[A/C]TGCAGCCCAGGAGTG	143279
rs780157005	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421883	TTATGGGAGGGTTTG[A/T]TCATTTTCATTATGC	143279
rs780201412	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91495322	GTTGTTCTAGTAGTT[C/G]TGACAGTATTGTGTT	143279
rs780274779	snp	A/G	1.6571e-05	0.0028784	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512273	CCCTAGCTTACCTGT[A/G]GCCCATACCTGCTTC	143279
rs780404423	in-del	-/GTTTA			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439070	TGCTGTGCAGGAGCT[-/GTTTA]GTTTAATTAGATGCC	143279
rs780408774	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440335	AGTTATTGAGAAAAT[G/T]GTGTGGTTTTTGTCA	143279
rs780428493	snp	G/T	0.000273547	0.0116918	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410489	TCCGCTGGTGGTGGC[G/T]GCGCCCGCGCCTGAG	143279
rs780495942	in-del	-/T	1.6522e-05	0.00287414	frameshift-variant, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512359	CATTGGAATTTCAAA[-/T]TTCAGAAGGTTTTGG	143279
rs780515404	snp	C/T			upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409906	CAGGCCAGGGCCGTC[C/T]GTGAAGGGTAGTCTG	143279
rs780516975	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412046	AATTTGCAAGTGTGG[A/G]TACAAGTCTACAGTC	143279
rs780525758	snp	A/G	1.65759e-05	0.00287883	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492337	TCTCCTCTACTGTAT[A/G]ATATCTTCAAATAGC	143279
rs780535473	snp	A/G	3.66764e-05	0.00428215	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498860	AATATGTGTAATGGC[A/G]TCTCCCATCAGGTTT	143279
rs780570792	in-del	-/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470181	AAACTAACAAAGATA[-/C]ATGGGACCTGAACTT	143279
rs780572950	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512217	GCATAGCAGTCATTT[G/T]GTGTGTGTTTCAAGA	143279
rs780600589	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476155	GAGAAACGGATGATA[C/T]AGGAGAGATAAGGAA	143279
rs780603413	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509881	AACCCCCATGACATG[C/T]AGTTTACCTTATATA	143279
rs780614365	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412589	CCTTGCTTGTGCCTT[A/G]TAAAGTCTTTCAGAG	143279
rs780663788	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485878	GTGGTTGTCCATTAG[A/G]TGCAATATAAAAAGA	143279
rs780680568	in-del	-/AC			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426568	TTTGCATACAAACAT[-/AC]ACACACACACACACA	143279
rs780682726	snp	C/T	1.7429e-05	0.00295199	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496402	ATTAATATCTTGTCC[C/T]TTAATGCGAAATCAT	143279
rs780772916	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460967	TGATAAAGATAGAAT[A/G]TAAACAAAGTCTCCA	143279
rs780788877	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91434266	TGTTATGACTAATCC[A/C]TTCTGGTCTTTCCTT	143279
rs780880526	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452039	CTCAACAACAGAATG[A/G]AGGGGATAGGAATCA	143279
rs780902866	snp	G/T	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410602	GGCCGGGGCCGTCTG[G/T]CGCCCCGGACGGCGG	143279
rs780908138	in-del	-/A			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458022	CATAATTGTCTATGC[-/A]AAAAAAAAAAAAAAA	143279
rs780969677	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431764	CTGTGTATTGCTTAT[A/T]CTAGTTATATATTCT	143279
rs780978280	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449171	GCGCATCAAAAAGCT[C/T]ATCTACCACGTGAGA	143279
rs780981256	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91453509	CAACTGGTAAAATGA[C/T]GATATGAGTAGCATG	143279
rs781059645	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91423870	CATTAGAATGATTAT[A/C]ATTTTAGTGGAACAA	143279
rs781062424	in-del	-/TTA			intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482894	GAATTTACCACGTAC[-/TTA]TTAAGCTTAGTGTCT	143279
rs781086071	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496473	TTACTTTTAAATATG[A/G]TTTCCTTCTACCTTT	143279
rs781091935	snp	C/T	1.66651e-05	0.00288657	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498226	TAATCATATATTTCA[C/T]ATATGAACAGTGCAA	143279
rs781105709	in-del	-/TAA	5.44786e-05	0.00521884	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482952	TAACACAATTATCTT[-/TAA]TATCTTTTTCAGAAT	143279
rs781172067	snp	A/G	3.60075e-05	0.00424293	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482953	AACACAATTATCTTT[A/G]ATATCTTTTTCAGAA	143279
rs781176681	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91495153	GATGCTGTAAAAAGC[A/G]TAATACTATATAGGA	143279
rs781233879	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490186	CTTTAAAAGACAACA[A/G]AGTTGAAATAGTACT	143279
rs781238223	snp	A/C/T	0.000160287	0.00895113	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410491	CGCTGGTGGTGGCGG[A/C/T]GCCCGCGCCTGAGGA	143279
rs781279752	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421528	AAAAAAAATTTATAA[C/T]GTTTTAAGAAAGTTT	143279
rs781324985	in-del	-/TTT			cds-indel, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91513574	GTCAGACAGTAAATG[-/TTT]TTTTTAATTTACAGC	143279
rs781338222	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509662	GCTCCATCCTAAGCA[A/C]ACTAACACAGGAACA	143279
rs781420774	snp	A/G	1.65559e-05	0.00287709	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492347	TGTATAATATCTTCA[A/G]ATAGCTAACCCGGAA	143279
rs781427835	snp	C/T			intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481157	AAGAGAACCAGAACC[C/T]AGTTGAAGTTGTCTA	143279
rs781449816	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91455319	CATTTCTCTGATGGC[C/G]AATGATGATGAGCAT	143279
rs781534170	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412875	TGTGGGGAGGGGGAG[A/G]AGGTCTTGATGTGTG	143279
rs781542127	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91466866	TGGAGAAACCTTAAA[C/T]ACATATTGCTAAGTG	143279
rs781552831	snp	A/G	0.000496335	0.0157455	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484604	GAATTTCCACCTATA[A/G]CAAAGTGTTCCTGGT	143279
rs781623994	snp	A/C	0.000295132	0.0121441	intron-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483092	GTAAATCATTCTATG[A/C]TATTAAGAACTTTTA	143279
rs781627249	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91465657	TGGGTATTGGATTTC[A/C]TCAACTGTTTCTTTT	143279
rs781644448	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471267	CTTTTGATAAAATTC[A/G]GCTTCCCTGCATGTT	143279
rs781656365	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91459331	AAACATGCAACTGCC[A/G]TATATTTACCTCAAA	143279
rs781658297	snp	C/T			intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91407880	TTGCACGTCTGACAC[C/T]TGGCATAGCTAAAAA	143279
rs781660506	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432426	TCAAATTGACTGTCC[G/T]TTTAAAAATAAGTGA	143279
rs781669664	snp	C/G	3.30978e-05	0.0040679	intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462220	GTAATATTATTCTGT[C/G]TCTCTTCTGTATATC	143279
rs781723628	snp	A/G			upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91408359	TATTTAGTCTCACAC[A/G]TGAAAAAAGAAAGCA	143279
rs796068002	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91504220	TAAAAATCAGAGCGC[C/T]TCTCCTCCTCCAAAG	143279
rs796068725	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412981	CTAGAGGTTTGCTTA[A/G]GAACCTAATTGTCAT	143279
rs796091826	in-del	-/A			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91469900	AGAACAATAGAAAAG[-/A]AAAAAAGAGCAGGGA	143279
rs796142119	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422534	AATATACAAGTAAGC[A/T]AACTTAGCCCCAGTC	143279
rs796159411	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91506357	TTTTGAAAGGATCAA[C/T]AAAATTGATAGACCG	143279
rs796174801	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91505147	TGGAAAGGAACAACC[G/T]GTACCAGCCGCTGCA	143279
rs796179000	in-del	-/A			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91424456	AAAGTGGATGTTAAA[-/A]GAAGTTAACTACTGT	143279
rs796183748	in-del	-/CGGGCC			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476890	GGATAAAAACCCCTG[-/CGGGCC]CGGGTCCGGGCCGGG	143279
rs796305878	in-del	-/A			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91480185	AGTAAAAATATCATT[-/A]AAAAAAATTCTAAGA	143279
rs796321323	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91413408	GTTACCTTGGTAGCA[A/T]ATTAAAGTCCTCATT	143279
rs796351396	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91480270	AAATGACCTTGCCAA[A/G]ATTATAAAGCTCTAG	143279
rs796498478	in-del	-/AA			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91418113	AATTCAGCTGAATTG[-/AA]AAAGTCAGTCTGAAA	143279
rs796503044	snp	A/G			intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482633	TCTTTTTCGATACTC[A/G]AAACAACCCTTAAGA	143279
rs796550545	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422513	ATTAAGATTTTCTGA[C/T]AACAAAATATACAAG	143279
rs796586003	snp	A/C			upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409735	GGCTGTCTCCCCGGG[A/C]TGCGCAAGCTCCGGG	143279
rs796648032	in-del	-/GT			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415194	TCCAAATTAGAGAAA[-/GT]GTGTGTGTGTGTGTG	143279
rs796677891	in-del	-/TTTTTTTTTAAACCACAAAGCCGTAAAGTCTCTTTGTCAACT			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415997	AGTCTCTTTGTCAAC[lengthTooLong]TTTTTTTTTAAACCA	143279
rs796712301	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91507695	AAAATGGCCATACTG[A/C]CCAAGGTAATTTACA	143279
rs796732689	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91506446	ATAAAGGGGATATCA[A/C]CACTGATCCCACAGA	143279
rs796739242	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91506391	GCAAGACTAATAAAG[A/G]AAAAAAGAGAGAAGA	143279
rs796744316	multinucleotide-polymorphism	CGA/TGT			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438314	TCAACTGCCACTTAC[CGA/TGT]TGAGAACATGCAGTG	143279
rs796855506	in-del	-/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91417701	GACATGAACTCATCA[-/T]TTTTTATGGCTGCAT	143279
rs796882938	in-del	-/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91465100	TAGTTTGGGTTTTTT[-/T]CCCCCCTCAGGGGTA	143279
rs796899598	in-del	-/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449943	ATATCATGAAAATGG[-/G]CCATACTGCCCAAAG	143279
rs796910254	snp	A/G			intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481901	ATATCAATATGTCTA[A/G]TGAAAGAACATATAC	143279
rs796910814	in-del	-/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421258	TTAACATTATTGACC[-/T]TTTTTTTTTCTTGAA	143279
rs796932932	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91506066	AATAAAGATGTTCTT[G/T]GAAACCAACGAGAAC	143279
rs796944567	in-del	-/A			intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91463076	AACAATGCGAGGGTT[-/A]GGGGCGCTAACCCCC	143279
rs796997188	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91505140	CTAAACATGGAAAGG[A/C]ACAACCGGTACCAGC	143279
rs796999434	in-del	-/A			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432679	ACTTTAAAAAAAAAA[-/A]TCTTTCCAGCCTAGG	143279
rs797004137	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91479086	AGATGTGGTTGCACC[A/G]TCCTGTAATTCCAGC	143279
rs797022277	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422252	TCCCTTTCTGATTCT[A/G]TATTCCAACTACACT	143279

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