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
rs410792	snp	C/T	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449363	TTCATGCTAAAAACT[C/T]TCAATAAATTAGGTA	143279
rs1329652	snp	C/T	0.340559	0.233022	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91486390	TAATAATTCTTGGCG[C/T]TGTTTTGTGGTTGTA	143279
rs1360187	snp	C/T	0.34101	0.232846	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501045	GGAATGGTGAGCTTC[C/T]ATATACGTATTAGAC	143279
rs2068724	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412008	AACCTATTCATCTCA[A/T]AACTGAAAAATTGCC	143279
rs2068725	snp	C/G	0.0244538	0.107838	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412217	TGCTAAAGGGAAAAA[C/G]TCAGTAGCGTCATGT	143279
rs2068866	snp	C/T	0.290201	0.246747	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91488632	ATTTATGCTTTAGGA[C/T]TCTTTTTATACTCTT	143279
rs2421517	snp	A/C	0.243633	0.249919	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461843	ATACAAGCCATCACA[A/C]CCAGCCCTTAAATGT	143279
rs2631678	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91413527	agaaattctgattta[A/C]caatactgcatttgg	143279
rs3834407	in-del	-/GA	0.375	0.216506	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487103	ATTTTCATAACCTTT[-/GA]TTATAATGTGTAATT	143279
rs3834408	in-del	-/A	0.144296	0.226554	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512698	GGGAAAGCAAAGTAC[-/A]GTGAAGAATGAATTT	143279
rs4376822	snp	A/G	0.298144	0.245321	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91480409	GGGTTTTGTTTTTCA[A/G]TCCAGGACCCAGTTA	143279
rs4405220	snp	A/G	0.00331674	0.0405878	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91488249	AGAAATATGCCCAAA[A/G]AAGGTGAAAGATGTT	143279
rs4415665	snp	A/G	0.336017	0.234736	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91430834	ttgactctttatcca[A/G]tttgccagtctgtgt	143279
rs4537674	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91428335	AGCTTTGTTCTTTTG[A/G]CTTAGGATTGACTTG	143279
rs4537675	snp	A/G	0.299158	0.245119	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91428403	aagtagttttttcca[A/G]ttctgtgaagaaagt	143279
rs4567363	snp	A/C	0.337386	0.23423	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431208	tgttgaatattggcc[A/C]ccactctcttctggc	143279
rs4590777	snp	G/T	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91436156	CTTTTGTCTGTTTGT[G/T]TTGGTCTCTGTCCTC	143279
rs5786959	in-del	-/A	0.0271762	0.113356	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91513341	ATCACCAGTTGTACC[-/A]AAAACACTAATTTTT	143279
rs6583775	snp	C/T	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457300	ggaacacttcttttt[C/T]gttttacaaagctgg	143279
rs6583776	snp	C/T	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91459489	tggaatactattaag[C/T]aataaaaatgaacta	143279
rs6583777	snp	C/T	0.340784	0.232934	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91495399	TTACACCTTAGCAAA[C/T]TGAAATTTTGGTGGT	143279
rs7071064	snp	A/T	0.139225	0.224118	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458854	acaccaaaagtacaa[A/T]ccataagagaaaaat	143279
rs7072087	snp	G/T	0.340333	0.233109	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482429	CAGAAGCTGTATGTG[G/T]TTCTCCCCTTGTTCT	143279
rs7074559	snp	C/G	0.243347	0.249911	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509048	caaacaccgcatatt[C/G]tcactcataggtggg	143279
rs7075344	snp	A/G	0.325563	0.238307	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509692	agaaaaccaaatacc[A/G]catattcttacttgt	143279
rs7075424	snp	A/G	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468865	cacttgagcccagga[A/G]ttcaaaactgtggtg	143279
rs7076784	snp	A/G	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432419	ATGCCTGTCAAATTG[A/G]CTGTCCTTTTAAAAA	143279
rs7076967	snp	G/T	0.0267878	0.112589	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409445	ATCTCTAACATAAAC[G/T]GAAAGGAACAAGGAA	143279
rs7077014	snp	C/G	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432299	TCTAACAGCTTGTTT[C/G]CCCGTCTGATCTTCA	143279
rs7081363	snp	A/G	0.325327	0.238382	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410192	GAGCCCCGGGCGGGC[A/G]GGGGAGGCGAGAGCA	143279
rs7081569	snp	C/G	0.000309885	0.0124437	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410493	CTGGTGGTGGCGGCG[C/G]CCGCGCCTGAGGAGA	143279
rs7081707	snp	A/G	0.138886	0.22395	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433203	TAACTGTTCCTATGG[A/G]AAGAGTTATTTTTTC	143279
rs7085276	snp	A/T	0.305685	0.24372	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493796	TTTAAGGCATTTTTT[A/T]AAAAAAATCAAAGTA	143279
rs7087338	snp	C/G	0.139225	0.224118	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458930	agaccctgtgcagag[C/G]atgaaaagacaggct	143279
rs7093711	snp	A/T	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502533	AGTAATCACACATGG[A/T]AAGTGCCCAATAGCT	143279
rs7098874	snp	C/T	0	0	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410013	CCCGACTGCCCGTCC[C/T]TAGTCCAGGTTCTCC	143279
rs7100516	snp	A/C	0.145305	0.227022	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497398	caggtccgagcaatt[A/C]tcctgcctcagcctc	143279
rs7100786	snp	A/G/T	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497484	ttttttttttttttg[A/G/T]atttttagtagagac	143279
rs7342052	snp	A/G	0.340559	0.233022	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432826	GTTTTTACACCCCCT[A/G]GAGAAAAGCATACTG	143279
rs7476690	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437641	tttttttttttttgg[G/T]tgttttgtttttttt	143279
rs7478184	snp	C/T	0.34146	0.23267	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91510215	CTAAAAGGGCATGAA[C/T]CCTTGGCAATATTTT	143279
rs7894248	snp	C/T	0.340333	0.233109	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476506	CCAGACTAAGAAGCC[C/T]CTAGGCTTCTCAGAA	143279
rs7895635	snp	A/C	0.139903	0.224452	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450691	caagaaaaaaaaaaa[A/C]catcaaaaagtgggc	143279
rs7895666	snp	C/T	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471636	aatgcaaaatcaata[C/T]ataaaaatcagtagc	143279
rs7898769	snp	A/T	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91417470	tggtgtgctgcaccc[A/T]ttaactcatcattta	143279
rs7898845	snp	A/T	0.340333	0.233109	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91480947	TATTTTCAGCATATT[A/T]TGGACTGTCTCAATA	143279
rs7899190	snp	G/T	0.00514135	0.0504405	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91494865	ATCACAATTTAGATT[G/T]GGATGATATTTTGAC	143279
rs7899549	snp	A/G	0.140242	0.224618	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451130	ccaacccaaatgccc[A/G]tcaatgatagactgg	143279
rs7900774	snp	A/G	0.326976	0.237854	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491711	GAGGTCTGACCTACA[A/G]GGTATATTGGGTCTA	143279
rs7904419	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415393	AGATATTACAAATAT[A/G]CAAAATAAGTGTTTA	143279
rs7904917	snp	C/T	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415632	TAACAGAGATGTTTC[C/T]GACTCATGTTCTTTG	143279
rs7906306	snp	C/T	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431688	ggctcctgaggcttc[C/T]gcattcttcacgtgg	143279
rs7907010	snp	G/T	0.347914	0.230028	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458015	gcagatggcataatt[G/T]tctatgcaaaaaaaa	143279
rs7908457	snp	A/G	0.340333	0.233109	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476242	caaatgaagggattg[A/G]ccttggtcaagtgca	143279
rs7908769	snp	C/T	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437169	ttttattcacaaata[C/T]gtaatttgtgtggag	143279
rs7910115	snp	A/G	0.190519	0.242821	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433979	AACTTTATAGAGAGG[A/G]GACTTTCAAATATTT	143279
rs7910297	snp	A/G	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471440	actcttagcactcct[A/G]ttcaacatagtactg	143279
rs7914133	snp	C/T	0.340559	0.233022	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485851	CATTTCTCATTTCTT[C/T]TGTAAGAAAAAGTGG	143279
rs7914794	snp	C/T	0.340559	0.233022	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91486315	ATATTTTCTTGGCAA[C/T]GTTTACTTTACAAAG	143279
rs7916523	snp	G/T	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421403	TCCTTATATTATCAG[G/T]TGTGTCCAATCTTTT	143279
rs7918822	snp	A/G	0.0283406	0.115616	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91466188	ttcagtaacatatct[A/G]ggttatcaaatttgt	143279
rs7919792	snp	C/T	0.202651	0.245475	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490933	aaGAGATGAGACATA[C/T]GGAAACTGTGATGCA	143279
rs7919797	snp	C/G	0.338976	0.23363	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91430769	attttgagcccatgt[C/G]tgtctctgcatgtgc	143279
rs7920553	snp	C/T	0.242488	0.249887	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91511950	ACTCGAACAAGACCC[C/T]ACAGCTAGTAAGTGG	143279
rs7920604	snp	A/G	0.17366	0.238059	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461320	TTTTTATCTAACAAC[A/G]TTTGATTCTTTCCCA	143279
rs7920790	snp	A/G	0.340559	0.233022	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431613	taaacttcccttctc[A/G]cttcatttcattcat	143279
rs9651433	snp	A/G	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420466	TGGTGGCATGTGCCT[A/G]TAATCCCAGCTACTC	143279
rs9664423	snp	A/C/G	0.0655868	0.168795	intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462266	AATATTGTAAAAATC[A/C/G]CCTTATAATTACCTT	143279
rs9732191	snp	A/T	0.338976	0.23363	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91456354	tgtgaatgggagttc[A/T]ctcatgatttggctc	143279
rs9732307	snp	C/G	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439217	ggttttaggtttaat[C/G]cttaagtctttaatt	143279
rs9732335	snp	A/C	0.0244538	0.107838	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439397	attgtagatgtgtgg[A/C]attatttctgagacc	143279
rs9761396	snp	G/T	0.375	0.216506	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449254	TGGATTACGTTTATT[G/T]ATTTGTGTATGTTGA	143279
rs9804186	snp	A/G	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438163	AGGTATACACGTGCA[A/G]TGGTGGTTGCCTGCA	143279
rs9804311	snp	C/T	0.34146	0.23267	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438314	TTCAACTGCCACTTA[C/T]GAGTGAGAACATGCA	143279
rs9943307	snp	A/G	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444679	CTGTTCTCACAGATG[A/G]TTCTTAAAATATAAT	143279
rs10450389	snp	A/G	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433492	tttctgtatcagtac[A/G]tagaaaacttcttta	143279
rs10786000	snp	C/G	0.00914312	0.0669923	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91414920	AGTGGGAAGCTATTG[C/G]AATTTCTGAAACAGA	143279
rs10786001	snp	A/G	0.0178098	0.0926698	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470986	GAGACACACACACAC[A/G]CACGCACACACACAC	143279
rs10881915	snp	C/T	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497091	cagcctcctgagtat[C/T]tgggattttaggcat	143279
rs11186558	snp	A/G	0.316726	0.240931	intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91407751	ACCCTATTCCCCATA[A/G]GTATAATTAATGAGC	143279
rs11186559	snp	A/C			upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91408290	CTTGCCTTGTTTTGC[A/C]AATATTTAAGCAGTT	143279
rs11186560	snp	C/T	0.340333	0.233109	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91411010	CTTCGCTTTTCTTTC[C/T]CTTCCCCCTTCAGAT	143279
rs11186561	snp	A/G	0.00793638	0.0624916	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412666	ACAGGATCTGTGGCA[A/G]AAtgtgtgtgtgtgt	143279
rs11186562	snp	A/G	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91416019	TTAAACCACAAAGCC[A/G]TAAAGTCTCTTTGTC	143279
rs11186563	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91418583	TGTACCTTGAAAGTA[A/G]CTGACTTTTCATATC	143279
rs11186565	snp	C/T	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91423701	TAATTCTAGAGACTT[C/T]TTAATTCTATGTGTA	143279
rs11186567	snp	A/G	0.190519	0.242821	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431670	CTTCCAGTTGATCGC[A/G]TCGGCTCCTGAGGCT	143279
rs11186570	snp	A/G	0.340333	0.233109	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91436326	TAGCCTGTTGATTGA[A/G]GAACCCTGATGTCCG	143279
rs11186571	snp	C/T	0.298905	0.24517	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91443496	TGCCAGCTGGAGCTC[C/T]CCTGTATGTGGTGTT	143279
rs11186572	snp	C/T	0.175897	0.238765	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445618	GAATAGGAACAGCTC[C/T]GGTCTGCAGCTCCCA	143279
rs11186573	snp	C/G	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91453218	AGGAGGATGGCCTGA[C/G]GCCAAGAGTTTGAGA	143279
rs11186574	snp	A/G	0.157972	0.232445	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457844	TCTTAATGGCTAAAG[A/G]CTTAGTGCTTTCCCT	143279
rs11186575	snp	C/T	0.192088	0.2432	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460347	CATTTGTTTTCTGTT[C/T]ATGTTGAATTAATCT	143279
rs11186577	snp	A/G	0.00716266	0.059414	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470994	CACACACACACGCAC[A/G]CACACACAGACACAC	143279
rs11186578	snp	C/G	0.0023933	0.0345097	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471003	ACGCACACACACACA[C/G]ACACACACGCACACA	143279
rs11186579	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471016	CAGACACACACGCAC[A/G]CACACAAAGAAAACC	143279
rs11186580	snp	C/T	0.340784	0.232934	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482066	AAACATATGTAGAGA[C/T]AGTAAAAGCTAGAAA	143279
rs11186581	snp	C/G	0.0138799	0.0821421	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483869	AACTCACGGCTAGCA[C/G]CACTGTAACTCATGC	143279
rs11186582	snp	G/T	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485519	TTTTGGTTTGGTTAA[G/T]AGCATCTTTTCAAGA	143279
rs11186583	snp	A/T	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485582	TATCTCTTACTATTC[A/T]ATGCAcaggggtcag	143279
rs11186584	snp	A/G	0.340784	0.232934	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91486918	TTGTACCACCTGACT[A/G]TGCTCAGAGGGATTC	143279
rs11186585	snp	A/G	0.330249	0.23677	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91494027	AAATTTTATAAGTCC[A/G]TCTGCAATCCTATGA	143279
rs11186586	snp	A/G	0.34101	0.232846	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91494804	ACTATACTATGAGCT[A/G]TTTATATGTTCATAC	143279
rs11186587	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497127	accgtgcccggcaaa[A/T]ttttttttttttttt	143279
rs11186588	snp	A/G	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497340	ctgttgtccaggcta[A/G]aatgcagtggaacaa	143279
rs11186589	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497527	TGTTGGCCAGGCTGG[G/T]CTTGAACTCCTGACC	143279
rs11186590	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497546	GAACTCCTGACCTTG[G/T]GATCTGCCCACCTCG	143279
rs11186591	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497614	GTGCCCGGCTAACCA[A/G]AAAATGTTTCTTTCA	143279
rs11186594	snp	A/C/T	0.0138799	0.0821421	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503224	GATACCATCTCACAG[A/C/T]GGTCAGAATGGCTAT	143279
rs11186595	snp	C/T	0.338976	0.23363	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503335	GAGCGACGCAGAAGA[C/T]GGGTGATTTCTGCAT	143279
rs11186596	snp	G/T	0.326035	0.238157	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91514035	TTTCATTTTGCTCTG[G/T]TTTAAATCCATATGC	143279
rs11186597	snp	A/G	0.341235	0.232758	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91514614	CAGTATTTTTTAAAC[A/G]TCCTGTCCTTTTTTA	143279
rs11318501	in-del	-/A	0.358515	0.225221	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432669	TCTTCCCCAAACTTT[-/A]AAAAAAAAAATCTTT	143279
rs11333012	in-del	-/T	0.2776	0.248472	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91416038	AGTCTCTTTGTCAAC[-/T]TTTTTTTTTAAACCA	143279
rs11492696	snp	G/T	0.175576	0.238665	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91454711	TCTCCTAATGCTATC[G/T]CTCCCCCCTCCCCCT	143279
rs11498512	snp	C/T	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91506892	AAAATACTGGCAAAA[C/T]GAATCCAGCAGCACA	143279
rs11498669	snp	A/G	0.295854	0.245759	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91506698	TCTACCAGAGGTACA[A/G]GGAGGAACTGGTACC	143279
rs11498670	snp	A/C	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91506891	TAAAATACTGGCAAA[A/C]CGAATCCAGCAGCAC	143279
rs11498671	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91508460	CATCAAAAAGTGGGC[A/G]AAGGACATGAACAGA	143279
rs11498672	snp	A/G	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91508705	TTCAACCATTGTGGA[A/G]GTCAGTGTGGCGATT	143279
rs11522500	snp	C/G	0.193966	0.243639	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91429428	CCCTCTTTTTCTATT[C/G]ATTGGAATAGTTTCA	143279
rs11639341	snp	A/G	0.221737	0.248397	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91504707	gaaaacactctgcag[A/G]atattatccaggaga	143279
rs12217566	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91427002	ctatccctcccccct[C/T]cccccaccccacaac	143279
rs12218668	snp	A/G	0.488726	0.0742286	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91418176	TTGGTTTTGTTCTAG[A/G]TGTTTTTGTTAAAAA	143279
rs12240287	snp	C/G	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450077	tatagtcaagacaat[C/G]ctaagcaaaaagaac	143279
rs12240706	snp	C/G	0.186105	0.241697	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420448	aaaaaaaaaagctgg[C/G]catggtggcatgtgc	143279
rs12240933	snp	A/G	0.0138799	0.0821421	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437969	TTAAAAAAACAATTT[A/G]TTAGAGCATAATTAT	143279
rs12241990	snp	A/G	0.243061	0.249904	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91508912	ggattaagaaaatgt[A/G]gcacatatacaccat	143279
rs12242257	snp	A/C	0.157642	0.232314	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450968	tgattcctcaagaat[A/C]tagaaccagaaatac	143279
rs12242663	snp	C/T	0.243633	0.249919	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481688	AAAGAAATTAAGATC[C/T]AGACAAATGAAAAGC	143279
rs12242821	snp	A/G	0.190519	0.242821	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421602	TGCACCCTGGGGGCT[A/G]TGGGTTGGACAAGCT	143279
rs12244852	snp	C/T	0.140242	0.224618	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91511827	tctctggccctgggg[C/T]tgggaactcctgGTT	143279
rs12245101	snp	A/T	0.0790232	0.182392	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512225	GTCATTTTGTGTGTG[A/T]TTCAAGACTTAGTAT	143279
rs12246881	snp	A/G	0.0134861	0.0810011	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91416291	GAAGTCTAAATTAAC[A/G]CACATAAAACATTTA	143279
rs12247442	snp	C/T	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91455005	tccaagtcttagcta[C/T]tgtgaatagtgccgc	143279
rs12247942	snp	C/T	0.339429	0.233457	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91428835	caaacagggacaatt[C/T]gacttcctcttttcc	143279
rs12249854	snp	A/T	0.340559	0.233022	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426505	TATAGGTTAGTATTT[A/T]TATTGCCTCATTTTT	143279
rs12250037	snp	C/G	0.29789	0.24537	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91429756	ttattgcatctattt[C/G]attcttctctccttt	143279
rs12250424	snp	C/G	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490611	AAGAGATGAGACATg[C/G]ccgggcgcggtggct	143279
rs12252076	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490745	aaatacaaaaaatta[C/G]ccgggcgtggtggtg	143279
rs12252082	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490764	ggcgtggtggtgggc[C/G]cctgtagtcccagct	143279
rs12253137	snp	A/G	0.340333	0.233109	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419322	TCAGTCTGTTCCTCA[A/G]TAGAGGTTGAAAGTA	143279
rs12255064	snp	A/G	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450156	taaccagaatagcac[A/G]gtactggtaccaaaa	143279
rs12257543	snp	C/T	0.0569829	0.158885	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444529	AAGAAAGGCAGAATC[C/T]TTTGCTCAGATTAGT	143279
rs12257663	snp	A/G	0.298398	0.245271	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497219	ggcctcaagtgatcc[A/G]cctgcctcagcctcc	143279
rs12258185	snp	G/T	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91430428	agttcaattcctggg[G/T]atccttgttaacttt	143279
rs12261288	snp	A/G	0.0850919	0.187897	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445809	cctcccctagccaag[A/G]gaagtcgtgagagac	143279
rs12262756	snp	A/T	0.306679	0.24349	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91429132	ctgcatctattgaga[A/T]aatcatgtggttttt	143279
rs12263089	snp	C/T	0.340559	0.233022	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452489	gcagtgttgagaggt[C/T]ggacctttaagaggt	143279
rs12265269	snp	C/T	0.339882	0.233284	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497106	ctgggattttaggca[C/T]gtgccaccgtgcccg	143279
rs12266111	snp	A/G	0.138886	0.22395	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91465959	cacagaaggacttag[A/G]aagtattctctctgc	143279
rs12266112	snp	A/G	0.186421	0.24178	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91465964	aaggacttagaaagt[A/G]ttctctctgcttctg	143279
rs12268013	snp	A/G	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419420	ACAGGTACTCTAAGT[A/G]TTTGTCTGTTTAAAT	143279
rs12269643	snp	A/G	0.243633	0.249919	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449761	atagccaaatcatga[A/G]tgacccccattcaca	143279
rs12354425	snp	C/T	0.00338409	0.040995	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420061	ATGCCCGTTTTTTTT[C/T]TCATGAAAGTCTTAG	143279
rs12355866	snp	A/G	0.0444908	0.142359	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91416661	gttaagtgacacatg[A/G]ttgTGTTTATAAAGC	143279
rs12358444	snp	A/G	0.00472811	0.0483911	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445473	GAAAAAGCAGTCTTA[A/G]AAGTATGGGACTGGG	143279
rs12359578	snp	C/T	0.040671	0.13668	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483512	AAAATATAGGCTAGC[C/T]ATCAATATCAATTTG	143279
rs12415354	snp	A/C	0.00396038	0.0443227	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91434245	GACAATGATGTAAAA[A/C]CCACTTGTTATGACT	143279
rs12761520	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450389	tcaagatggattaaa[A/G]acttaaatgtaaaac	143279
rs12761521	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450395	tggattaaaaactta[A/C]atgtaaaacctaata	143279
rs12761546	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450424	tactgtgaaaactct[A/G]gaagaaaacctaggc	143279
rs12763130	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450406	cttaaatgtaaaacc[C/T]aatactgtgaaaact	143279
rs12763152	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450421	taatactgtgaaaac[C/T]ctagaagaaaaccta	143279
rs12768965	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497112	ttttaggcatgtgcc[A/C]ccgtgcccggcaaat	143279
rs12770078	snp	A/G	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490598	AACTTTGCTATTTAA[A/G]AGATGAGACATggcc	143279
rs12775063	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91435904	tttcttttttacttg[G/T]atttctcttctcttt	143279
rs12775728	snp	A/G	0.0185938	0.0946107	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461114	AAGAATTATAAATCC[A/G]TAAACTATATTAACT	143279
rs12778255	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91418955	GTTTTTATATGCATC[A/G]CAGATTCTTGGACTC	143279
rs13376715	snp	A/T	0.243633	0.249919	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471540	aaatctttgcagatg[A/T]tattattctatacct	143279
rs13376868	snp	A/G	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91434973	ACAATGTATGTAGAT[A/G]AGCAGTTTAGTTGTG	143279
rs17093783	snp	A/C	0.0271762	0.113356	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91514088	CACTGCTTGAACTAG[A/C]AAATCAGCTTTTTAA	143279
rs17106657	snp	G/T	0.340559	0.233022	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426637	TAAGGAGGCACCTTT[G/T]AGTTCACACTCTAAT	143279
rs17106676	snp	C/G	0.0271762	0.113356	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460844	TAATTAAATAATAGA[C/G]TGTTACCATTTTTAG	143279
rs17106706	snp	G/T	0.140242	0.224618	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512695	ACTGGGAAAGCAAAG[G/T]ACAGTGAAGAATGAA	143279
rs28836802	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91507449	ATACAAAATCAGTGT[A/G]CAAAAATCACAAGCA	143279
rs28859028	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91507119	AGGTATTGATGGGAC[A/G]TATTTCAAAATAATA	143279
rs34031656	in-del	-/GT/GTGTGTGTGTGTGTGT	0.0023933	0.0345097	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415194	CCAAATTAGAGAAAG[-/GT/GTGTGTGTGTGTGTGT]TGTGTGTGTGTGTGT	143279
rs34096833	snp	A/C	0.444444	0.157135	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452439	TGAGTATTTATTTCC[A/C]CCAAAATTCATGTTG	143279
rs34157168	in-del	-/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421052	CCCCTCAGGCTTTTT[-/T]CCCCTTCAGTAAAGC	143279
rs34166692	in-del	-/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91514524	TGTAGTTACTTTTTT[-/T]ACATATATAATCTGT	143279
rs34254753	in-del	-/TT	0.375	0.216506	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497481	TTTTTTTTTTTTTTT[-/TT]GGATTTTTAGTAGAG	143279
rs34302420	snp	C/T	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471670	TCTATACACCAACAT[C/T]TAAGCAGAGAGCCAA	143279
rs34402156	in-del	-/C			intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462610	TTGTAACAAGTTCCC[-/C]AGGATATGTTGATTT	143279
rs34422401	in-del	-/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91489790	CTCCAAATTAGTGTT[-/G]TTATTATAGTAATCT	143279
rs34483967	in-del	-/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476336	CCTAGAAAGCTTCCC[-/C]TGTCCCAGGCAGGTA	143279
rs34500938	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497357	ATGCAGTGGAACAAT[C/T]TCAGCTCACTGCAAC	143279
rs34553731	snp	A/G	0.00959175	0.0685848	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500606	TCACTTTATAGTTAA[A/G]TCCGTTTTTGCATAG	143279
rs34591206	in-del	-/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91494120	TCTACATTAGCTTTT[-/T]AGATTCCAAGAAATG	143279
rs34606737	in-del	-/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91411405	GACATAATATTTAAG[-/C]TACTTTTTGAAAGTT	143279
rs34670314	in-del	-/G			intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482922	GTCTTTCCTTTTACG[-/G]TGTTAACAGAATTTT	143279
rs34718593	snp	A/G	0.030278	0.119257	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512067	TTGTCTGTAACCACA[A/G]CCTTAGTGTCTAGAG	143279
rs34782955	in-del	-/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91475105	ATTGTATGGTAATGG[-/G]AAAGTCATTGAGTGT	143279
rs34784301	in-del	-/G			frameshift-variant, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492444	TTGACTAAAGAATGG[-/G]TTCCTTCTTCTAATT	143279
rs34801372	in-del	-/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419539	GTGAAATAAGATTTT[-/T]GGTTAGTTATTGTAA	143279
rs34836601	in-del	-/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91510633	AATGTTATTGAATGG[-/G]ATGCATGAAACACTG	143279
rs34852217	in-del	-/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458651	GGAAAAATAACCTTT[-/T]CAATAAATGGTGCCA	143279
rs34865895	in-del	-/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91465896	GATCTATACTTTTCC[-/C]TTTCTTGTAATATCT	143279
rs34939219	in-del	-/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91418447	GCGTTGATTTTTTTT[-/T]GTGACAAAATTTTGT	143279
rs35085085	in-del	-/G			upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91408612	AAGCAGAAAATAATG[-/G]TTATGTTCCTCTCTA	143279
rs35165435	in-del	-/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477946	GTTATATAAAAATTC[-/C]TGTTGGTCATCAACC	143279
rs35201953	in-del	-/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91465790	ATAAATCACACTTGG[-/G]TTGTGTTGTATAATT	143279
rs35268555	in-del	-/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91486842	AAGCCATCTCACTTT[-/T]CAGTTTACACTAAGG	143279
rs35321363	in-del	-/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91511363	GCATCTACTGTCCCC[-/C]AAAATGCTCTTTTTT	143279
rs35338875	in-del	-/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91454624	TGTACAACATGTAGG[-/G]TTTGTTACATATGTA	143279
rs35403049	snp	C/T	0.0236746	0.106192	intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91463202	TAAACAGTCAATTAA[C/T]GTATATTTTATGTTA	143279
rs35412589	in-del	-/A			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91435512	AAAGGCAGTCAGGGT[-/A]CTTGGTGATGACAAG	143279
rs35460330	in-del	-/G			intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482269	TTTCACAATTTCAGG[-/G]AGGTTTTTTTCAATA	143279
rs35478503	in-del	-/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477435	AGCACATTTGTTTGG[-/G]TTTTTCTCCTGCAGC	143279
rs35518057	in-del	-/T			intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462403	TATCCAATCCTTTTT[-/T]AGAAAGACTTGCTAA	143279
rs35529459	in-del	-/A/AA	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468957	AAAAAAAAAAAAAAA[-/A/AA]CAAGAGTACAGTTGC	143279
rs35573602	in-del	-/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440454	GGTGGATAAGCTTTT[-/T]GATGTGCTGCTACAT	143279
rs35581877	in-del	-/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464729	GTTGGAGCACACACC[-/C]ATGCTACCTGTGCAC	143279
rs35618355	in-del	-/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91511298	GATAGTAGGTGGGGG[-/G]AGATGACACCAAAAG	143279
rs35649537	in-del	-/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438337	ACATGCAGTGTTTGG[-/G]TTTTCTATTCCTATG	143279
rs35719024	snp	C/T	0.030278	0.119257	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91504107	AACAGAAAGGACATC[C/T]ACACCAAAAACCCAT	143279
rs35719750	in-del	-/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490616	TGAGACATGGCCGGG[-/G]CGCGGTGGCTCACGC	143279
rs35745527	in-del	-/A			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91414304	GGAAGACAAGGGGAA[-/A]GAGTTTGAGGGTGAG	143279
rs35765581	in-del	-/A			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91495673	CTCCAAGTAACATAA[-/A]GTCTTTCAAGTTTTA	143279
rs35912153	in-del	-/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91428733	ATTGATTTTGTATCC[-/C]TGAGACTTTGCTGAA	143279
rs35926209	in-del	-/ATAA	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444756	CCTCAAACTGACATT[-/ATAA]ATAGAGGCAAATCTT	143279
rs36198704	snp	A/G	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449526	CCTATACAACATAGT[A/G]TTGGATGTTCTGGCC	143279
rs41286930	snp	A/G	4.94727e-05	0.00497332	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460472	TTAGACAAAAACAGC[A/G]TACATCTATGGATGC	143279
rs41286932	snp	C/G	0.0107246	0.0724382	intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462478	TATATTGGAATTACA[C/G]TGAATCTGTAGATCA	143279
rs55667468	snp	A/G	0.338523	0.233803	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426974	CATTTAGCATTAGGT[A/G]TATCTCCTAATGCTA	143279
rs55680455	in-del	-/A			intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482523	TTTTTCTAGCTTTTA[-/A]TCAAGGAACACCCAG	143279
rs55704027	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91443769	CAAAATACTACGAAA[C/T]ACTCTTCCATGGTTT	143279
rs55718133	snp	C/T	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440352	TGTGGTTTTTGTCAT[C/T]GGTTCTTTTTAAGTG	143279
rs55762845	snp	A/T	0.324145	0.238752	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412631	GATTATTTATTTTTT[A/T]AAAAAAAAAACAATT	143279
rs55814310	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91446616	AGGCAAGGAAGCTGT[A/G]AACCTTGATAAAAGG	143279
rs55907162	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444435	GCCCAGATGGGATTT[A/G]TTTTTAGTTGAAAAG	143279
rs55909420	snp	A/G	0.0103295	0.0711199	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500286	GTTTTTCTGGCAAAC[A/G]GCTAATTACTATTTA	143279
rs55916968	snp	G/T	0.00676609	0.0577691	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91429130	TTCTGCATCTATTGA[G/T]AAAATCATGTGGTTT	143279
rs55990545	snp	C/T	0.0119091	0.0762411	intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91463900	TCTCCTAACATGAAG[C/T]ATATGCATATTCTGT	143279
rs56097320	snp	A/G	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449176	TCAAAAAGCTCATCT[A/G]CCACGTGAGAGAACT	143279
rs56923120	in-del	-/TT			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497154	TTTTTTTTTTTTTTT[-/TT]AGCAGAGACGGGGTT	143279
rs57033814	snp	C/T	0.311859	0.242226	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91408522	TATCTGAAATTGCAG[C/T]TAAAATAAAGGCTTC	143279
rs57090051	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496965	TGTAAGAAAATCTTT[C/T]TTTTTTTTTTTTGAG	143279
rs57105282	in-del	-/A			frameshift-variant, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487731	GTAGCTGCAAAAAAA[-/A]TCATTATTCAGAGAG	143279
rs57159565	snp	C/T	0.186421	0.24178	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476115	TCTGCGTTGTTATAC[C/T]GATAGGAATGTTTTA	143279
rs57281864	snp	A/C	0.340333	0.233109	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91418678	AACTGTGAAAAAAAA[A/C]CATACAAAAAGAGAA	143279
rs57314370	snp	A/G	0.239037	0.24976	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471012	CACACAGACACACAC[A/G]CACACACACAAAGAA	143279
rs57937605	in-del	-/A			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477202	AAAAAAAAAAAAAAA[-/A]CCCCTGCGGGTCCAA	143279
rs57988119	snp	C/G	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499508	TTACAACTTCTTAAT[C/G]ATTAAGGAACATATG	143279
rs57998663	in-del	-/AATA			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444759	CAAACTGACATTATA[-/AATA]GAGGCAAATCTTTGT	143279
rs58135026	in-del	-/G	0.340333	0.233109	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490232	TTCCTACTTTCTTCA[-/G]GTGTACCTTCCTTGT	143279
rs58167250	in-del	-/A	0.354019	0.227333	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91424453	TTAAAAGTGGATGTT[-/A]AAAGAAGTTAACTAC	143279
rs58209119	in-del	-/A			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493695	ACTTAATTGAAAGAA[-/A]TGAGAGTTTGATTTT	143279
rs58234316	in-del	-/CA			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426584	ACACACACACACACA[-/CA]AGCACACACACACCC	143279
rs58238306	snp	G/T	0.0360663	0.129354	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91423090	TATAAAAGTAGAGAT[G/T]ACATCAGCCACAAAG	143279
rs58290272	in-del	-/AAG	0.316968	0.240864	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91408651	TATTTCAGTAGTTTT[-/AAG]AAGGAAAGAAAATCC	143279
rs58296918	in-del	-/A	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420295	CAAAAAAAAAAAAAA[-/A]GAAAATCAGGCTGGG	143279
rs58350586	snp	C/G	0.0107246	0.0724382	intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91407738	CCCACCCTGCCAAAC[C/G]CTATTCCCCATAGGT	143279
rs58548755	in-del	-/T	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91434628	TGTTCTTCTTTTTTT[-/T]GGGACATCTTATAGT	143279
rs58691011	in-del	-/GTGT/GTGTGTGT	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412695	TGTGTGTGTGTGTGT[-/GTGT/GTGTGTGT]ATTTGTCAAAGAGAG	143279
rs58916172	in-del	-/AT			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438540	AGTGCTGTAATAAAC[-/AT]GTGTGTGTGTCTTGA	143279
rs59198703	snp	G/T	0.247905	0.249991	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503648	CGGAGTCTCGCTGAT[G/T]GCTAGCGCAGCAGTC	143279
rs59758370	snp	C/T	0.186421	0.24178	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503628	GCTCGGAGGGTCCTA[C/T]CCCACGGAGTCTCGC	143279
rs59785873	in-del	-/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437638	TTTTTTTTTTTTTTT[-/T]GGTTGTTTTGTTTTT	143279
rs59929049	snp	G/T	0.0279526	0.114869	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477250	TAGCAAGGTCATAGC[G/T]AGGAATGATGCTGGG	143279
rs60132366	in-del	-/G	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449941	CAATATCATGAAAAT[-/G]GGCCATACTGCCCAA	143279
rs60167819	snp	A/G	0.0119091	0.0762411	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451451	GTGCCGGAAACCACC[A/G]TGGCATATGTATACC	143279
rs60231237	snp	A/T	0.0115144	0.0749975	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512239	GTTTCAAGACTTAGT[A/T]TTTTTTTTTAATTTT	143279
rs60618386	in-del	-/GTG	0.340559	0.233022	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412007	AACCTATTCATCTCA[-/GTG]TAACTGAAAAATTGC	143279
rs60640820	snp	A/G	0.316968	0.240864	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91408513	AGCACAGAATATCTG[A/G]AATTGCAGCTAAAAT	143279
rs60649813	in-del	-/GTGTGTGTGT			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415231	TGTGTGTGTGTGTGT[-/GTGTGTGTGT]ACTTAACAACAATAT	143279
rs60938850	in-del	-/TCTC			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496439	TCTACCTGCACAGTC[-/TCTC]CTCCTAATGCTATTC	143279
rs61035151	in-del	-/A			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490919	AAAAAAAAAAAAAAA[-/A]GAGATGAGACATACG	143279
rs61346715	snp	A/G	0.187369	0.242028	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91418680	CTGTGAAAAAAAACC[A/G]TACAAAAAGAGAAAC	143279
rs61474836	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438562	TGTGTCTTGATAGTA[A/G]AATGATTTATCTTCC	143279
rs61579794	snp	A/C	0.159622	0.233092	intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91463068	GACCCTTGAACAATG[A/C]GAGGGTTAGGGGCGC	143279
rs61606120	snp	C/T	0.0123036	0.0774623	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91436474	TCTCTCTTGATTGGT[C/T]AATCACTTAGTATTC	143279
rs61754653	snp	C/G	0.00207742	0.032162	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498116	TTTATAGGAGTTGGC[C/G]CATGGATTAAGTGAA	143279
rs61754654	snp	A/T	0.0122419	0.0772729	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460485	GCGTACATCTATGGA[A/T]GCATCATCATCCGAA	143279
rs61754655	snp	A/G	0.00725504	0.0597904	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461261	CATTTTAGGGAAGAT[A/G]TAGAAAAAGTTAAGT	143279
rs61877863	snp	A/T	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420299	AAAAAAAAAAAAGAA[A/T]ATCAGGCTGGGTGCA	143279
rs61877864	snp	A/T	0.0178098	0.0926698	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91427806	TGTAGGTTGCGAAAA[A/T]TTTTTCCCATTTTGT	143279
rs61877867	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91429958	TTTTTCTAGTTCTTT[C/T]AACTGTGATGTTAGG	143279
rs61877868	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438957	AATTTGTTGAAGTTC[A/C]TTGTAGATTTTGGAT	143279
rs61877869	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438997	TTGTCAGATGGATAG[A/G]TTGCAAACATTTTCT	143279
rs61877870	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439002	AGATGGATAGATTGC[A/G]AACATTTTCTCCATT	143279
rs61877872	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439018	AACATTTTCTCCATT[C/T]TGTAGGTTGCCTCTT	143279
rs61877873	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439031	TTCTGTAGGTTGCCT[C/G]TTCACTCTGATGATA	143279
rs61877875	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439065	TCTTTTGCTGTGCAG[A/G]AGCTGTTTAGTTTAA	143279
rs61877876	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439070	TGCTGTGCAGGAGCT[C/G]TTTAGTTTAATTAGA	143279
rs61877877	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439087	TTAGTTTAATTAGAT[C/G]CCATTTGTCAATTTT	143279
rs61877878	snp	A/G	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449496	ACAGAAGACAAGGAC[A/G]CCCTCTCTTACTACT	143279
rs61877880	snp	C/T	0.040671	0.13668	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467863	CTGCAAAAATGCACA[C/T]GGACACTAGCAACTA	143279
rs61877892	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91507360	GCAGATGACATGATT[C/G]TATATCTAGAAAACC	143279
rs61877893	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91507368	CATGATTGTATATCT[A/G]GAAAACCCCATTGTC	143279
rs61877894	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91508670	AACACTTTTACACTG[C/T]TGGTGGGACTGTAAA	143279
rs62006507	snp	C/T	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449228	ATTGAACCAGCCTTG[C/T]GTCCCAGGGATGAAG	143279
rs62085443	snp	C/T	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449389	TATTATTTTGAGATA[C/T]GTCCCATCAATACCT	143279
rs62326573	snp	A/G	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449235	TGCGTATATTGAACC[A/G]GCCTTGCATCCCAGG	143279
rs71025355	in-del	-/C	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410609	CCCAACTCCCGCCGT[-/C]CGGGGCGCCAGACGG	143279
rs71479082	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482458	CTTTGTGATATATGA[A/G]GCTAACTCATTTTAC	143279
rs71949434	in-del	-/GTGT			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412676	GGCAGAATGTGTGTG[-/GTGT]TGTGTGTGTGTGTGT	143279
rs72128875	in-del	-/AATT	0.0119091	0.0762411	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91495051	TATTTCAAGTTAAAC[-/AATT]AAATCTAAAAATTAT	143279
rs72815495	snp	G/T	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91408855	ATATTAAAGTAGAAA[G/T]CCTTTCTATAAATGA	143279
rs72819209	snp	A/G	0.0329836	0.124112	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91414572	ATATGTAAAAACCAC[A/G]ATGAGCCATAGAAAC	143279
rs72819210	snp	A/G	0.00318978	0.0398085	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440211	TATGATATTAGCTGC[A/G]GCTTTGTCATAAATA	143279
rs72819214	snp	C/T	0.00279162	0.0372561	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91469638	AAGACTGTTACCGGC[C/T]GCCACAAAAACACAC	143279
rs72819215	snp	A/T	0.0322114	0.122752	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91472983	TAAAAATAATAAAGA[A/T]GTATAGAGGTTAGAA	143279
rs72819217	snp	C/T	0.0174175	0.0916809	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476812	GAGCACCTGTGAGGC[C/T]TTTGTCTTTGGCTGG	143279
rs72819219	snp	C/T	0.0185938	0.0946107	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481534	TATTTTCCCATCTAG[C/T]AGGTTTTCACTTCAC	143279
rs73316216	snp	C/T	0.340333	0.233109	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91416196	CAAAAAAGTCAAGTA[C/T]GATTCTGCTTTGCTG	143279
rs73316246	snp	A/G	0.190519	0.242821	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91466793	ACTGTGGTACATTCC[A/G]TATCATGGAAATTAT	143279
rs73316255	snp	C/T	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91480993	CCTAGTTTTTGGCTT[C/T]TCTCAACTCAGTCTT	143279
rs73316259	snp	A/G	0.0166325	0.0896639	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484943	TAAATGGCCATCTGC[A/G]TATTCCCTTTAATAC	143279
rs73316284	snp	A/G	0.144296	0.226554	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500319	AGATCTATAAACTTC[A/G]GAAGCAAAAATATCT	143279
rs73316291	snp	A/G	0.0174175	0.0916809	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91514318	AAATTTTTAGATGAC[A/G]AAGTCCATAAATAAC	143279
rs74149207	snp	G/T	0.0119091	0.0762411	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419562	TATTGTAATTACTAC[G/T]TTTTTCTGCTGTTTG	143279
rs74149208	snp	A/C	0.0150606	0.0854603	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419639	CCTAGAGAGTCAGGT[A/C]TATTATTTATTAGGT	143279
rs74149209	snp	C/G	0.0119091	0.0762411	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421013	TGCATAGTAGATCTT[C/G]CCTCAAACCTTTGCA	143279
rs74149211	snp	G/T	0.0119091	0.0762411	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91424759	AAAAAAATTCTGGTA[G/T]GCCCAATCACAGTGC	143279
rs74149212	snp	A/C	0.00755907	0.0610114	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91424804	ACTCTAAAGGGTTAT[A/C]TTTTTACCTGAACTT	143279
rs74149213	snp	A/G	0.0119091	0.0762411	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432415	AGGTATGCCTGTCAA[A/G]TTGACTGTCCTTTTA	143279
rs74149215	snp	C/G	0.0119091	0.0762411	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444057	ATAGTCATCTCCTCT[C/G]TTCAACACCAGTCTT	143279
rs74149218	snp	A/G	0.0119091	0.0762411	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91454272	AATGGATCATATTCT[A/G]GGCCATAAAACAACT	143279
rs74149221	snp	A/C	0.0119091	0.0762411	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467567	CTGGGGCATAGCTCA[A/C]CAGCAGACCACTCCT	143279
rs74149234	snp	A/C	0.0490535	0.14873	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91473424	AAACTGCCTTTACCA[A/C]CAACAGACGTATACT	143279
rs74149236	snp	G/T	0.0119091	0.0762411	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91474192	AATAACTTTCTTAAC[G/T]GGAGAGTAGGGGAAT	143279
rs74149237	snp	A/G	0.0119091	0.0762411	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476389	CACCACACCTGCTCA[A/G]TCACCCAGAAATAGG	143279
rs74149239	snp	A/G	0.0119091	0.0762411	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91494303	CAATGTATTTTTCCC[A/G]GAGAGGATAGAGATT	143279
rs74321605	snp	A/C/G/T	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449383	AAATTAGGTATTGAC[A/C/G/T]GGACGTATTTCAAAA	143279
rs74326832	snp	A/C	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449225	GAACCAGCCTTGAAT[A/C]CCAGGGATGAAGCTG	143279
rs74332424	snp	A/C	0.375	0.216506	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449232	ATATATTGAACCAGC[A/C]TTGCATCCCAGGGAT	143279
rs74364545	snp	C/G	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444232	AAATTAACTTATTCA[C/G]ACACAGAGCATATAT	143279
rs74467159	snp	A/T	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432679	ACTTTAAAAAAAAAA[A/T]TCTTTCCAGCCTAGG	143279
rs74495696	snp	A/G	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471214	AATCATGTGGTTTTT[A/G]TCTTTAGTTCTGTTT	143279
rs74546958	snp	C/T	0.00517822	0.0506191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91479941	TATCCTTTTATAAGT[C/T]TTCCACCTACTTTTG	143279
rs74581054	snp	A/C	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451928	ATTTCATTATTATAG[A/C]CCTTAAAATCTATAA	143279
rs74639251	snp	A/C	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449236	TTGCATATGTTGAAC[A/C]AGCCTTGCATCCCAG	143279
rs74650963	snp	A/G	0.139225	0.224118	intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462807	GAGAACCATACTGCT[A/G]TAGATCAATTTGTGA	143279
rs74670987	snp	A/C	0.0486741	0.148216	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91459764	GTCCCCTAGATTATA[A/C]TACTATATTTTTACT	143279
rs74711831	snp	A/T	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449362	CTTCATGCTAAAAAC[A/T]CTCAATAAATTAGGT	143279
rs74745574	snp	C/T	0.0383715	0.133092	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482754	AATTAGCCCTCAGAC[C/T]CAGATCTGTCTTAAC	143279
rs74815269	snp	A/G	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449369	CTAAAAACTCTCAAT[A/G]AATTAGGTATTGATG	143279
rs74882783	snp	A/G	0.0185938	0.0946107	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492538	CATAATTGTTAGAGT[A/G]AAGTAGTCACCCTTA	143279
rs74887456	snp	C/T	0.0387552	0.1337	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409650	CGCACTCCTCCCCAC[C/T]TCCAGGCTTTTCCTG	143279
rs74933208	snp	C/T	0.00557542	0.0525036	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425721	TATGTAATGGATATC[C/T]CATATTTGAGCAATA	143279
rs74979969	snp	A/C	0.00517822	0.0506191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426643	GGCACCTTTTAGTTC[A/C]CACTCTAATTTCTAT	143279
rs74992644	snp	A/G	0.0275645	0.114116	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91475185	CAGAAAATGGTCTGT[A/G]GTGTGTCAAGAGAAA	143279
rs75086698	snp	C/G	0.611111	0.124226	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471273	GTAAAATTCCACATC[C/G]CTTCATGTTAAAAAC	143279
rs75191395	snp	C/T	0.0425829	0.139564	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91495616	ATAAATAATCCTGAG[C/T]AAAATTTGTAACATC	143279
rs75339987	snp	A/G	0.0240643	0.107019	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91495205	TTGTGGTCAGGTAAG[A/G]AGTTGGGAACTGAAA	143279
rs75353616	snp	C/T	0.0240643	0.107019	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91459198	AACTATCAAAAATAA[C/T]GACACCACCAAATGC	143279
rs75489763	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91469044	GATTCTCCTAAATAG[C/T]TCAGTCAGACAAAAA	143279
rs75494572	snp	C/G	0.0306952	0.120022	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477473	GCTCAGGGGCAAACA[C/G]TAAGTGGTTGAGCAG	143279
rs75499195	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467548	TGCCCAACCAAGGTA[A/C]TTCCTGGGGCATAGC	143279
rs75595353	snp	A/T	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471938	CTACCAATGACATTC[A/T]TCACTGAATTAGAAA	143279
rs75621038	snp	A/C	0.00517822	0.0506191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91465910	CCTTTCTTGTAATAT[A/C]TTTCTCTTTTGAGCA	143279
rs75662313	snp	A/G	0.030665	0.119967	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433666	CTCTGTACATATGTC[A/G]CTTTGTTCATCTGCA	143279
rs75664166	snp	C/T	0.0271762	0.113356	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91413438	TCCTACATCTCACCC[C/T]AGAGCACCTGTTTTC	143279
rs75702719	snp	A/G	0.00993419	0.0697739	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91434359	GGGATCCTTCAACTT[A/G]TAGCTCATTTATTAT	143279
rs75714152	snp	G/T	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502230	ATCTACCAGTTTTCA[G/T]TTCTTTCTATGCTTT	143279
rs75727580	snp	A/G	0.0248432	0.108648	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410790	ACACCTACCACCCTC[A/G]GGAAATGTTGGGGGT	143279
rs75742049	snp	C/G	0.0119091	0.0762411	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470579	TATAAATCTAAATGC[C/G]TACATCAAAAATGTT	143279
rs75770938	snp	G/T	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449394	TTGATGGGATGTATC[G/T]CAAAATAATAAGAGC	143279
rs75827527	snp	C/G	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419478	TTACATATAATCTAT[C/G]TGATTATATCATCAA	143279
rs75887891	snp	A/G	0.0119091	0.0762411	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457268	TGTACAATCTCTACC[A/G]GAAAATAGACGAAAA	143279
rs75960787	snp	C/T	0.00279162	0.0372561	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458304	AGTGTAAAGGCATAC[C/T]GTGTTCATGGATTAG	143279
rs76070020	snp	C/T	0.157642	0.232314	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439227	TTAATCCTTAAGTCT[C/T]TAATTCATCTTGAGT	143279
rs76071173	snp	A/C	0.375	0.216506	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449375	ACATCCCATCAATAC[A/C]TAATTTATTGAGAGT	143279
rs76355341	snp	C/T	0.375	0.216506	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449124	ATTGATGCAAAAATC[C/T]TCAATAAAATACTGG	143279
rs76522006	snp	A/G	0.0271762	0.113356	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415066	GCCACAGGACAGAGT[A/G]TAAGGGATGGGAGCA	143279
rs76592016	snp	A/C	0.0174175	0.0916809	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91472301	ACAATATACAAAAAT[A/C]AACTCAAGACAAATT	143279
rs76595201	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91472096	TCTGTTTTTGTACTA[C/G]TACCATGCTGTTTTG	143279
rs76608596	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512173	GTGAAATAGATTTGA[A/G]TGTGTGTGTCCTGGT	143279
rs76727931	snp	C/T	0.00874735	0.0655527	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91456863	ATAAAATCAGTGAAA[C/T]TGAAAACAGAAAAAT	143279
rs76733435	snp	A/C	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449100	TTTAGACCAATATCC[A/C]TGATGAACATTGATG	143279
rs76801282	snp	C/T	0.0119091	0.0762411	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468455	TGAACGAATGTCAAC[C/T]CACTCAGATGAGAAA	143279
rs76802730	snp	G/T	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91505924	CTATAACAAACTATC[G/T]CTCAGACCACAGTGC	143279
rs76855484	snp	C/T	0.0252325	0.109451	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509924	ATGTACCCCTGAACC[C/T]AAAATAAAAGGTAGA	143279
rs76876752	snp	G/T	0.375	0.216506	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91505964	AGAACTCAGGATTAA[G/T]AATCTCACTCAAAGC	143279
rs76876864	snp	A/G	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420295	CAAAAAAAAAAAAAA[A/G]GAAAATCAGGCTGGG	143279
rs76933514	snp	A/G	0.0023933	0.0345097	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457692	AAACCTGCAATTAAC[A/G]TTTTATGTAGTTGTG	143279
rs76989045	snp	C/T	0.46875	0.121031	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449248	ATGTTTATTGATTTG[C/T]GTATGTTAAACCAGC	143279
rs77023499	snp	A/G	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471912	GGTAGTTTGATAGGA[A/G]TAGAATTAAATCTGT	143279
rs77068203	snp	A/T	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449148	ATACTGGCAAACCGA[A/T]TCCAGCAGCACATCA	143279
rs77083627	snp	A/G	0.0023933	0.0345097	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467590	CCACTCCTGACCATC[A/G]TAGGGTCCAGCAGAG	143279
rs77116173	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452996	CTTGAGATGTGAGGA[A/G]AGGGGAAAGAAGGTG	143279
rs77117715	snp	A/G	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420442	TACAAAAAAAAAAAA[A/G]GCTGGGCATGGTGGC	143279
rs77188327	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449084	AAAAAAAAAAGAAAA[A/T]TTCAGGCCAATATCC	143279
rs77217947	snp	A/G	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471951	TCATCACTGAATTAG[A/G]AAAAAAAAACTATTT	143279
rs77305076	snp	A/C/G	0.0287504	0.116538	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91413763	CAGTAGAAATCAGGC[A/C/G]TGGTGGGGAATTGAA	143279
rs77365372	snp	C/T	0.375	0.216506	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449099	TTTCAGGCCAATATC[C/T]CTGATGAAACTCGAT	143279
rs77395094	snp	A/G	0.0486741	0.148216	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91414323	TTTGAGGGTGAGCAT[A/G]AGGTGTGTCGAGAGA	143279
rs77418731	snp	C/T	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449365	CATGCTAAAAACTCT[C/T]AATAAATTAGGTATT	143279
rs77451747	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91434791	TTGAATTCTAGCTCC[A/G]TAACATACAAACTGT	143279
rs77688461	snp	A/C	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450692	AAGAAAAAAAAAAAC[A/C]ATCAAAAAGTGGGCA	143279
rs77702525	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431840	ATTTCCTCCTGTAGC[G/T]CGTAGTTTGATCGTC	143279
rs77757595	snp	G/T	0.00478085	0.0486577	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509697	ACCAAATACCACATA[G/T]TCTTACTTGTAAGTG	143279
rs77814765	snp	A/C	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450690	ACAAGAAAAAAAAAA[A/C]CCATCAAAAAGTGGG	143279
rs77935307	snp	C/T	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449111	ATCCCTGATGAACAT[C/T]GATGCAAAAATCCTC	143279
rs77969496	snp	A/G	0.0271762	0.113356	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415812	AATCATGGGAAAGAT[A/G]TGTTCTAGGATATCT	143279
rs77975415	snp	A/G	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449246	AGGCTGGTTCAACAT[A/G]CGCAAATCAATAAAC	143279
rs78002787	snp	A/G	0.144969	0.226867	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476105	GTGATGTTAGTCTGC[A/G]TTGTTATACTGATAG	143279
rs78075614	snp	A/G	0.0275645	0.114116	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91475094	CATGCAAGTTTAATT[A/G]TATGGTAATGGAAAG	143279
rs78076723	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91416429	AATGCCTTTTCTGTT[C/T]AGATATGTTTAGATG	143279
rs78154484	snp	A/C	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449233	TGTATGTTGAACCAG[A/C]CTTGCATCCCAGGGA	143279
rs78164599	snp	A/G	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449335	AAAGGCCTTTGACAA[A/G]ATTCAACTGCCCTTC	143279
rs78182738	in-del	-/TAA	0.00932878	0.0676562	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493389	TTAAGTCAATCATGT[-/TAA]TAATAACATTATTCG	143279
rs78316581	snp	C/T	0.0452528	0.143452	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91454376	ATAACAGGAGCATCT[C/T]CAAAATACTTGGAAA	143279
rs78400350	snp	A/C	0.00517822	0.0506191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500060	TTTAATCTCTGTAGG[A/C]GGTAGACTAACCCAC	143279
rs78472585	snp	A/C	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468943	ACTGTCTCACTCAAA[A/C]AAAAAAAAAAAAAAC	143279
rs78608093	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91453097	GTTGAAACAAAAATT[A/G]TAACACCAGCGTGGT	143279
rs78610098	snp	A/T	0	0	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481741	TTGAGGAAGAAATAC[A/T]TTATTACCATAGCTA	143279
rs78704150	snp	A/G	0.00874735	0.0655527	intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91407704	TTCCAGGGAAATAAT[A/G]AGTTCTCTAACCCTC	143279
rs78725237	snp	A/T	0.0275645	0.114116	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91480186	AGTAAAAATATCATT[A/T]AAAAAATTCTAAGAA	143279
rs78736775	snp	A/G	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471914	TCAGTAGTTTGCTAG[A/G]AATAGCATTGAATCT	143279
rs78757252	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426351	ACACCCTAACCAAAC[A/C]AAACAAACCTAGAAA	143279
rs78769766	snp	G/T	0.139564	0.224285	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422074	AGACTGCTACCATAG[G/T]GATTTTTTTCTAAAA	143279
rs78802668	snp	A/G	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420293	TACAAAAAAAAAAAA[A/G]AAGAAAATCAGGCTG	143279
rs78820827	snp	C/T	0.0193772	0.0965046	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91494436	GGGCTTGGTAGAGAG[C/T]AGCAGCAAGCGCACT	143279
rs78903138	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471970	TTTTGGTTCCAYATG[C/T]ATTTTAAAATAGTTT	143279
rs78910834	snp	A/G	0.0486741	0.148216	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444688	CAGATGATTCTTAAA[A/G]TATAATTCAAAAAGA	143279
rs79110488	snp	A/G	0.00478085	0.0486577	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460143	GGAAAGAAATGCTAA[A/G]TTACATTAACAAACA	143279
rs79111467	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449243	TTATGATTTGTGTAT[A/G]TTGAACCAGCCTTGC	143279
rs79118386	snp	A/C	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449081	TATTGGTCTAAAATT[A/C]TCTTTTTTGGTTGTG	143279
rs79158368	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483206	ATATTCACAATGCTT[A/C]AAAAGCCAGTTACAA	143279
rs79165698	snp	C/T	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91472057	ATCTTGTAATATAGT[C/T]TGAAGTTGAGTAACA	143279
rs79168137	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478006	GCTACACATACCAGG[G/T]ATACTCTTACTGTAA	143279
rs79192080	snp	A/C	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449368	ATCAACACCTAATTT[A/C]TTGAGAGTTTTTAGC	143279
rs79211652	snp	A/C	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471023	ACACGCACACACACA[A/C]AGAAAACCTCAGGCC	143279
rs79311005	snp	A/T	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512251	AGTATTTTTTTTTAA[A/T]TTTTTTCCCTAGCTT	143279
rs79400986	snp	A/G	0.0244538	0.107838	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445220	GCCACATGATTAGGG[A/G]ATTGATAACTGTTCC	143279
rs79411656	snp	C/T	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449146	ATGTGCTGCTGGATT[C/T]GGTTTGCCAGTATTT	143279
rs79532967	snp	A/G	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431881	TTCTTCTCTCGACTC[A/G]TCAAAGTCATTCTCC	143279
rs79601487	snp	C/T	0.0119091	0.0762411	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457586	ATAATTTGACAAAAT[C/T]CAACACCTATTCATA	143279
rs79615444	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91427789	AAAATTTTCTCCCAT[G/T]TTGTAGGTTGCGAAA	143279
rs79675242	snp	A/C	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420282	GCTTTTATGATTACA[A/C]AAAAAAAAAAAAAGA	143279
rs79737798	snp	A/G	0.0240643	0.107019	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91488729	TGAGTATTTCTTTCT[A/G]TCACAGAGAAGGACA	143279
rs79837339	snp	A/C	0.375	0.216506	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91505849	CACACCACACCTATT[A/C]CAAAATTGACCACAT	143279
rs79856746	snp	C/G	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503051	TTGAATATTCATTCA[C/G]TAGATTTTTGTTAAA	143279
rs79869631	snp	A/G	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420296	AAAAAAAAAAAAAAA[A/G]AAAATCAGGCTGGGT	143279
rs79870737	snp	C/G	0.095934	0.196885	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412855	GCTAGGAAGGCCTTG[C/G]TATGTGTGGGGAGGG	143279
rs79909213	snp	A/T	0.046775	0.145601	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91466237	AATAGTCATAAATTA[A/T]CCTTTTAATGTCTAT	143279
rs79928483	snp	C/G	0.0244538	0.107838	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410958	GAGGTGCCTGCCTGC[C/G]TGCCTGCCTTGGAGG	143279
rs80032692	snp	C/T	0.0429648	0.14013	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91479968	TTTGCCATTTTTTAT[C/T]GCAGATTTGCCTGAT	143279
rs80099715	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410609	GCCGTCTGGCGCCCC[C/G]GACGGCGGGAGTTGG	143279
rs80200256	snp	G/T	0.00358779	0.0422022	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431290	GTGGGTAACCCAACC[G/T]TTCTCTCTGGCTTCC	143279
rs111261920	snp	C/T	0.444444	0.157135	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91416821	CTTTATAAACCTCCA[C/T]CGTCCCCCTCACCTC	143279
rs111264717	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492892	AGAATTCATGAATTA[A/C]TTTTTTAAGAAAAAA	143279
rs111271955	snp	A/G	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476521	TCTAGGCTTCTCAGA[A/G]ACAGGGCAGACAGAG	143279
rs111309031	snp	A/G	0	0	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410148	TTGACGAGGGGGACT[A/G]CCGCCGGCGCTCCCG	143279
rs111358393	snp	C/T	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501640	AATGTTCATTTTTAT[C/T]TAAATGTGAAATGTG	143279
rs111361031	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91448983	TTCCACCTGAAACTA[C/T]TCTAAACAACAGAAA	143279
rs111465573	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91448674	AATCAAATAGACACA[A/T]TAAAAAACGATAAAG	143279
rs111475807	snp	G/T	0.00874735	0.0655527	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91479911	AACATTTTATCATTT[G/T]TTGCTATTTTTATTT	143279
rs111551484	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91447332	AAATGCTGAGAGATT[C/T]TGTCACCACCAGGCC	143279
rs111583851	snp	A/G	0.18989	0.242666	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503948	AACAGGCAGACTGCC[A/G]CCTCAAGTGGGTCCC	143279
rs111608011	snp	C/T	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425608	ATGAAATACAAAACT[C/T]GTGAATAATAAGCAA	143279
rs111629000	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91447491	TGATCGTGTCATTAT[A/G]ATGCTAGCTGTTTAT	143279
rs111631819	snp	C/T	0.0618563	0.164627	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91434790	TTTGAATTCTAGCTC[C/T]GTAACATACAAACTG	143279
rs111641207	in-del	-/CT	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91416582	ATTTGTATAAGTACA[-/CT]CTGTGATGTTTGCAC	143279
rs111643758	snp	A/G/T	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445975	ATTTGAGCAGACACC[A/G/T]AACTTGCTGCAGGAA	143279
rs111651622	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487952	ACAATTTGGGAGACA[A/C]GATAACTCTCATCTC	143279
rs111679609	snp	A/G	0.5	0	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500572	TGCATGCTCTGCAGA[A/G]AAGTACTCAGTATGA	143279
rs111692040	snp	A/C/G	0.139564	0.224285	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420496	CAGGAGGCTGAGGCA[A/C/G]GAGAATCAGTAGAAC	143279
rs111731488	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481455	ACAGAATGGAAGCAC[C/T]TCTTCCTCCTCCATT	143279
rs111763278	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91505966	AACTCAGGATTAAGA[A/C]TCTCACTCAAAGCCA	143279
rs111778827	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91430285	ACATTTGCTGAGGAG[A/G]GCTTTACTTCCAAGT	143279
rs111841889	snp	C/T	0.00438332	0.0466095	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451446	GATGGGTGCCGGAAA[C/T]CACCATGGCATATGT	143279
rs111866072	snp	C/T	0.243633	0.249919	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450646	caaagggctaatatc[C/T]agaatctacaaggaa	143279
rs111871435	snp	A/T	0.5	0	upstream-variant-2KB, intron-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409327	GTGGAGGTGGGGGGT[A/T]TTTTAATTTCATAAT	143279
rs111886488	snp	A/C/T	0.000348068	0.0131878	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461231	TTCTATATGTATATA[A/C/T]GGTTAATGTGTTTTC	143279
rs111889497	snp	A/G	0.139564	0.224285	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438942	TTGATTTTTCTTGCA[A/G]ATTTGTTGAAGTTCC	143279
rs111912355	snp	A/G	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91465167	TTGAACTAAACAAAC[A/G]AGTAAATATATCAAT	143279
rs111917656	snp	C/T	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91418640	AGCATTTCATGATTT[C/T]GTAACCCACCATCCT	143279
rs111936662	snp	A/G	0.0178098	0.0926698	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91443450	CTGTTCCTTCCTCTG[A/G]AAGCTTTGTCCCAGA	143279
rs111944395	snp	C/T	0.00398564	0.0444627	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91411245	GGGTTATTTGGAGAG[C/T]GCTGTCAGGCTTCAA	143279
rs111955010	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91447342	AGATTCTGTCACCAC[C/G]AGGCCTGCCTTACAA	143279
rs111989228	snp	A/T	0.00438332	0.0466095	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91480736	AGCATATTTTCTTTC[A/T]TTAATACATAAATGT	143279
rs111999349	in-del	-/T	0.338296	0.233889	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412455	TACAAAACTTGAGGG[-/T]TTTTTTTTTTTTCTT	143279
rs112003082	in-del	-/C	0.139225	0.224118	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440181	AGGGAATGCTTCCAG[-/C]TTTTGCCCATTCAGT	143279
rs112026917	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91441930	TTTTGCTTTCCATTT[G/T]TGTGGGAAATATTCC	143279
rs112156820	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91513665	TACTTTAACAGCTTT[C/T]CTTCAGAAAACTCTG	143279
rs112173014	snp	A/C	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433643	GCAGACAATGCCACA[A/C]TGAATGACTCTGTAC	143279
rs112226806	snp	C/G	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476908	GGTCCGGGCCGGGCG[C/G]GGTGGCTCATGCCTG	143279
rs112249993	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91507479	ATTCTTATACACCAA[C/T]AACAGACAAACAGCC	143279
rs112258937	snp	A/G	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485929	GCCTTACCACAGCTT[A/G]TTTATTATAATAATT	143279
rs112314220	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91442222	CAGTGGCTGGTACCA[A/G]TTTTCCTTTCCATAT	143279
rs112340404	snp	C/T	0.5	0	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498134	TGGATTAAGTGAACT[C/T]TTATCACATGAAGGC	143279
rs112489054	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440282	TGAGAGTTTTTAGCA[G/T]GAATGGGGTGTTGAA	143279
rs112491442	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450958	GATGGTGTGGTGATT[C/T]CTCAAGAATCTAGAA	143279
rs112498667	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91407748	CAAACCCTATTCCCC[A/G]TAGGTATAATTAATG	143279
rs112531458	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499375	CCCTTCTACTAAGTC[C/T]TTTAGAGCTTTACAA	143279
rs112536398	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91507062	AGAAAAGGCCTTTGA[C/T]AAAATTCAACAACGC	143279
rs112581557	snp	C/T	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91510857	GTTTTTTAAGTCAGA[C/T]TGATCTGGGTCTGAA	143279
rs112596242	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91430140	TTTCGTTATGTACCC[A/T]GTAGTCATTCAGGAG	143279
rs112601724	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91429175	GTTTATATGCTGGAT[G/T]ACATTTATTGATTTG	143279
rs112620253	in-del	-/AAAG	0.243919	0.249926	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471022	CACACGCACACACAC[-/AAAG]AAAACCTCAGGCCAA	143279
rs112678461	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478510	TTAAATTGTATGTAA[A/G]GTTTTTTCTATGCAG	143279
rs112725424	snp	C/T	0.0611083	0.163768	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450404	AACTTAAATGTAAAA[C/T]CTAATACTGTGAAAA	143279
rs112753764	snp	A/G	0.0174175	0.0916809	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91488228	AAAGTGTGTCTTGGA[A/G]AACTGAGAAATATGC	143279
rs112787598	snp	C/T	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491379	TTATAAAAATCATAG[C/T]AAACTTTTTTATTTC	143279
rs112790924	in-del	-/TG	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500674	GAACAGCAGACAGTG[-/TG]GTTCATTTATTTGCA	143279
rs112803175	in-del	-/C	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91418679	ACTGTGAAAAAAAAC[-/C]ATACAAAAAGAGAAA	143279
rs112808115	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91469416	ACCTTTGAGCAGAAA[C/T]CCTTCAAGACAGAAG	143279
rs112825421	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91459338	CAACTGCCGTATATT[C/T]ACCTCAAAGAAATGA	143279
rs112838068	snp	C/T	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91423231	CAGATTTCATGGTCA[C/T]TCAAACTGGAGTTTG	143279
rs112954618	snp	A/G	0.5	0	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484518	CCAGATTGTCCCAGA[A/G]GAGGTTCAAACAATT	143279
rs112955574	snp	A/T	0.00318978	0.0398085	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461046	TAAGGATGATCTTTT[A/T]TAAAAATAAGTAAAT	143279
rs113052172	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499350	CACCCCAGTCAGTTC[A/G]TTTTCTCTCCCCTTC	143279
rs113105866	snp	A/G	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501464	ATCTTCAGAGTAAAC[A/G]TGGCCTTGAAATGTA	143279
rs113108141	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438540	AGTGCTGTAATAAAC[A/G]TGTGTGTGTGTCTTG	143279
rs113116194	snp	A/C	0.196456	0.247571	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91454790	TGTTCTCATTGTTCA[A/C]TTTCCACCTGTGAGT	143279
rs113118944	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440978	TCTCTTTTCTTCTTT[A/G]TTCGTCTGGCTAGTG	143279
rs113150082	snp	A/G	0.0614824	0.164198	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91454525	GCTACAGCAGTGCTG[A/G]GAGGGAAATTTATAG	143279
rs113184485	in-del	-/T	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445991	AACTTGCTGCAGGAA[-/T]TTTTTTTTTTATAAC	143279
rs113195755	in-del	-/T	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426851	CTTGAACTTGGGGTA[-/T]TTTTTTTTATTATTA	143279
rs113239106	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91441084	TCTATCTCCTTCAGT[C/T]CTGCTCTAAACTTAG	143279
rs113244089	snp	A/G	0.0244538	0.107838	intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91489285	CATTATCAGTTTTTT[A/G]TGGGTGTTTCCCAAC	143279
rs113314450	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425849	ATCTAAAGACCAAAA[G/T]GTAGTTTGAATGGAA	143279
rs113327266	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91441742	TTATGACTCTGGGTA[C/T]TCCTGTATTGGGTGC	143279
rs113344259	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91466362	TCTCTTCAAAAAAAA[A/G]TCAGCATTTTGTTGT	143279
rs113416881	in-del	-/A	0.339882	0.233284	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420429	CTCTACTAAGAATAC[-/A]AAAAAAAAAAAAAGC	143279
rs113450507	snp	A/T	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478110	TCAAGTCTGATTTTA[A/T]CTATTGAAACAGATC	143279
rs113454180	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491726	GGGTATATTGGGTCT[A/G]TACAGGTTCTAACAT	143279
rs113460100	snp	G/T	0.00398564	0.0444627	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432525	TGATAAATGATAGAG[G/T]AGAGGAGGTTAGCAC	143279
rs113467056	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91505657	AAAGAGACTTAGACT[C/G]CCACACATTAATAAT	143279
rs113477679	snp	C/T	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501565	TTTTACTTTGCTAGG[C/T]CATATAAGTGCTTTG	143279
rs113627904	snp	G/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91436858	ACTGACATCTCTGCT[G/T]CTTTTTACCTTTGAG	143279
rs113643223	snp	A/C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462265	AAATATTGTAAAAAT[A/C/T]ACCTTATAATTACCT	143279
rs113658584	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449305	AAAAACACTTAATTA[A/C]CTCAATAGATGTATA	143279
rs113689362	snp	A/G	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490708	CATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTC	143279
rs113722068	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91507527	CCATTCACAACTGCT[A/T]CAAAGAGAATAAAAT	143279
rs113734501	snp	G/T	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425628	ATAATAAGCAAATTT[G/T]ATTAAAGAGGTGGCT	143279
rs113739277	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451724	AAACCCCCACACTAA[C/T]GAAATTTATCTTTGC	143279
rs113811339	snp	C/T	0.5	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471345	AGGAATCGTCTGTGA[C/T]AAACCCACAGCCAAC	143279
rs113899704	snp	G/T	0.0263992	0.111815	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91417768	TCCAGTCTATCATTG[G/T]TGGACATTTGGGTTG	143279
rs113900644	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449085	ACAAAAAAAGAAAAT[C/T]TCAGGCCAATATCCC	143279
rs113905082	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91428547	TTATATCCTCTTTTA[C/T]TTCATTGAGCAGTGG	143279
rs113933491	snp	A/G	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438885	TGTCTTCTTTTAAGA[A/G]GTGTCTGTTCATATC	143279
rs113986375	in-del	-/G	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91469336	AATGAATGAAAAAAT[-/G]TTAAAGGCAGCTACA	143279
rs114135463	snp	A/G	0.0383715	0.133092	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500725	CAATTAAGTTAGTCA[A/G]AATATTAGAGAGTCC	143279
rs114352174	snp	C/T	0.0240643	0.107019	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457095	CAATTCCTCAAAAAA[C/T]AAAAGCTATTGCAGC	143279
rs114433783	snp	A/G	0.00279162	0.0372561	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91413945	TGTATGGATATGAAG[A/G]GCTGATGATGTGAAT	143279
rs114448770	snp	C/G	0.0244538	0.107838	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415662	GCCCAATTCTGAACA[C/G]TCGACATTTGCGGTC	143279
rs114474691	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91511928	TGGGATTTGGGGATA[C/T]TATGCAACTCGAACA	143279
rs114532589	snp	A/G	0.0040338	0.0447284	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500570	TATGCATGCTCTGCA[A/G]AGAAGTACTCAGTAT	143279
rs114561852	snp	C/T	0.0325976	0.123435	intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91463850	TGATGTAAGTATAAA[C/T]TGGTACAACCACTTT	143279
rs114564197	snp	A/G	0.0271762	0.113356	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422220	TACCTTCCCAGTCAT[A/G]TCTTGCTGGACCATT	143279
rs114576418	snp	A/T	0.00478085	0.0486577	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419668	GTTGAAATAAATACA[A/T]ATCTATTATTTAAAG	143279
rs114724408	snp	A/G	0.0158469	0.0875917	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452194	GTCCCAGAAGGAGAG[A/G]AAAAGACAGTAGGGC	143279
rs114784427	snp	C/G/T	0.00517822	0.0506191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500118	AAGACAGACTATAAC[C/G/T]AAGTGCCCAAACTCT	143279
rs114881518	snp	C/G	0.00478085	0.0486577	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91466270	AATCAGTGTGAGAAT[C/G]ATCTTTCATTTAGTA	143279
rs114904404	snp	A/G	0.00478085	0.0486577	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490211	AGTACTGTAAACACA[A/G]TTTTATTTCCTACTT	143279
rs114917389	snp	C/T	0.0271762	0.113356	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91479029	TGTCAGTCTGGCCAA[C/T]ATGGTGAAACCCCAT	143279
rs114964653	snp	A/G	0.00755907	0.0610114	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458876	GAGAAAAATTTATCA[A/G]TTTGACTTCATCAAA	143279
rs114999855	snp	C/T	0.0174175	0.0916809	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415664	CCAATTCTGAACACT[C/T]GACATTTGCGGTCAT	143279
rs115067310	snp	A/G	0.0271762	0.113356	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503266	AAAGTCAAAAAATGA[A/G]GGAGGAGCCAAGATG	143279
rs115084987	snp	C/T	0.00438339	0.0466099	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460581	GTAAGTTTCAGCTAT[C/T]ATATGTAAATGTATA	143279
rs115119445	snp	C/T	0.0325976	0.123435	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91511806	GGCCACCAACAACCA[C/T]ACCCATCTCTGGCCC	143279
rs115144900	snp	C/T	0.00492436	0.0493754	synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425367	AGAAGCTGCTGAAAA[C/T]AGAAGTTCACCTGCA	143279
rs115165792	snp	C/T	0.0425829	0.139564	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492277	AGACTGCCTAACACA[C/T]TTCCCAGAATTAAAA	143279
rs115242581	snp	A/G	0.00676609	0.0577691	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91489383	TCTTACAAATAGTCA[A/G]TGTAAGCAAGAGCTT	143279
rs115315827	snp	C/G	0.0240643	0.107019	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477465	CTTTTGTTGCTCAGG[C/G]GCAAACACTAAGTGG	143279
rs115387354	snp	C/T	0.0387552	0.1337	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458780	TAAATTATTGGACTT[C/T]TAGAAAAAAAATGAA	143279
rs115438842	snp	A/T	0.00478085	0.0486577	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91466271	ATCAGTGTGAGAATG[A/T]TCTTTCATTTAGTAA	143279
rs115440963	snp	A/G/T	0.0387552	0.1337	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512742	ACCCAGTGGCAGATT[A/G/T]TACACTGCTAGCACT	143279
rs115446963	snp	C/G	0.0271762	0.113356	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91443696	CAGTCGCCCCTTCCC[C/G]CAGGAAGAATTTGTA	143279
rs115524669	snp	A/G	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432739	GACATTTACCTTGAG[A/G]GCAAGCTCATAGCCA	143279
rs115562626	snp	A/C	0.0486741	0.148216	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499714	CCTTTCAGTCACCCC[A/C]GCTACCCAGCACACA	143279
rs115605753	snp	A/C	0.0260105	0.111035	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91469418	CTTTGAGCAGAAACC[A/C]TTCAAGACAGAAGAG	143279
rs115883504	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464792	ATGACACAGCCCACC[C/T]CACAGCCACTCAGCC	143279
rs115908906	snp	A/G	0.00478085	0.0486577	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496632	GCTCTGTGAATTTGG[A/G]CAAGTTATTTAACCC	143279
rs115985032	snp	A/G	0.0146672	0.084371	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499620	GTTATGGTGGACTCA[A/G]TTTGGTCTGACTTGT	143279
rs115985431	snp	A/G	0.0260105	0.111035	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91434233	AGTCATCCTATAGAC[A/G]ATGATGTAAAAACCA	143279
rs115990620	snp	A/T	0.0111196	0.0737302	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91414592	GCCATAGAAACAATT[A/T]GTACTATCAGAGATG	143279
rs116062296	snp	C/T	0.0325976	0.123435	intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91408014	AGTTGGGAATGTGTC[C/T]CTCAAGCACACCACG	143279
rs116127279	snp	C/T	0.0271762	0.113356	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91489830	TAAGTAGCCTTAAAT[C/T]GTAGATTTGTGATAC	143279
rs116173425	snp	A/G	0.00517822	0.0506191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501981	CATTGAACATTCCCT[A/G]AGTGCTCTTAGTTCT	143279
rs116213176	snp	C/G	0.0271762	0.113356	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482122	TGAGTATATTGGTCA[C/G]CCATAAGCTCTGCTC	143279
rs116246243	snp	C/G	0.0379877	0.132479	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91465874	CATCTATGTTCATGA[C/G]AGGTATTGATCTATA	143279
rs116295758	snp	G/T	0.0240643	0.107019	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487365	CTCCCTCCTGGTTCT[G/T]GTATTGGCCATGTTG	143279
rs116386081	snp	A/G	0.00874735	0.0655527	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499679	TATTTAGAATACCAT[A/G]TCAGAAGTATCATAG	143279
rs116390178	snp	A/T	0.0134861	0.0810011	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415046	GTGCATCCACTAAGG[A/T]GGTGGCCACAGGACA	143279
rs116438573	snp	C/G	0.0240643	0.107019	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91475124	GTCATTGAGTGTTTT[C/G]GGCAGGGATCATTTA	143279
rs116488171	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433113	ACAGGTTTCCTTAAA[C/G]AATGAACTGATTTTA	143279
rs116611263	snp	A/G	0.00517822	0.0506191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490410	ATTGGGATAAAGGAT[A/G]TGAATATTGTGATGG	143279
rs116732929	snp	A/G	0.0325976	0.123435	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91473592	TTTTATTCCGCCTCT[A/G]CCATGTCTGAGACAG	143279
rs116920797	snp	C/T	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91459450	TGGTTGAATAGTTAA[C/T]CATATAGCGGTACAC	143279
rs117051037	snp	A/G	0.00279162	0.0372561	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467666	CAGAACCTCCCCTCC[A/G]TAGCTTTGCCAGCAT	143279
rs117142383	snp	A/T	0.00438332	0.0466095	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91472581	GGTCTAATATCCAGA[A/T]TCTATAAAAAACTGA	143279
rs117144859	snp	C/G	0.030278	0.119257	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471197	AAATGTGATTCATCA[C/G]GTAACAGAACTAAAC	143279
rs117261962	snp	C/T	0.0174175	0.0916809	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432491	TAGTGATGATATCTC[C/T]TCAGAGAAACAACCT	143279
rs117588698	snp	A/C	0.0850919	0.187897	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452939	ATTTACTCTAAAAGA[A/C]TAAAGGAGTTCTCTA	143279
rs117679427	snp	G/T	0.0134861	0.0810011	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461542	AGTATATGGGTTTTT[G/T]GAGGGGGTTGTTTTG	143279
rs117761150	snp	A/G	0.02016	0.0983543	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91510799	ATGTATGTCTGGTGC[A/G]TAAAAAATTAAGAAT	143279
rs118071562	snp	A/C	0.00438332	0.0466095	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422143	CAATGATTTTTCTCT[A/C]TCTCTGTTCAGGATA	143279
rs118108658	snp	A/G	0.0165278	0.0893908	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470178	AAGAAACTAACAAAG[A/G]TACATGGGACCTGAA	143279
rs118119919	snp	A/G	0.00716266	0.059414	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91435618	TTCCTGTTCCTTTGA[A/G]TCAGATGTCTCTCTA	143279
rs118144312	snp	A/T	0.0023933	0.0345097	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415028	TCATGCCTGAGGCAA[A/T]GAGTGCATCCACTAA	143279
rs118182931	snp	A/G	0.0123036	0.0774623	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444223	TTCAAATATAAATTA[A/G]CTTATTCACACACAG	143279
rs137867844	snp	A/G	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432264	CTCTTCTCTGGTAGT[A/G]GGACCTATGCTGGGT	143279
rs137937830	snp	A/G	0.00279162	0.0372561	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477687	CCTCTTTCATGTAAC[A/G]TGACACAAATTTTAC	143279
rs137957667	in-del	-/TA	0.0275645	0.114116	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457458	ATATGTAAAAAGAGT[-/TA]TATACACCATGACCA	143279
rs138012676	snp	A/C	0.00478085	0.0486577	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439281	AAGGATTCCAGTTTC[A/C]GTTTTCTGCATATGG	143279
rs138110296	in-del	-/A	0.188631	0.242351	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91454065	CCTGAACCCAGAAAC[-/A]AAAAAATCCACAATT	143279
rs138138057	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487271	TTCTGGAACTCACAC[A/G]TCAGAAGTCACCATA	143279
rs138141146	snp	C/T	0.0115144	0.0749975	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502149	CGTGGGAAATAACTT[C/T]ATTGCCAGTTTAAGT	143279
rs138212999	snp	C/G	0.00636936	0.0560724	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91427480	CAACAGTGTAAGAGT[C/G]TTCCTGTCTCACCAC	143279
rs138219455	snp	A/C	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91494765	TTTCATCTTCATTGA[A/C]GGGCCTAATCATTGA	143279
rs138279937	in-del	-/ATA			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91495114	ATCACACACACAGAT[-/ATA]AAACCTATAGAAAGC	143279
rs138289031	snp	A/C	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470690	AGAAATAACCAAAAT[A/C]GGAGTTGAACTGAAA	143279
rs138316283	in-del	-/AG	0.0205511	0.0992634	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91456753	TGAGATACGTCAAAA[-/AG]GGGGAAAGTTTCAAA	143279
rs138331649	snp	C/T	0.0193772	0.0965046	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450178	GTACCAAAACAGATA[C/T]ATAAACCAATGGAAC	143279
rs138337856	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91413950	GGATATGAAGGGCTG[A/G]TGATGTGAATATTAA	143279
rs138414842	snp	A/G	0.000307953	0.0124049	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425372	CTGCTGAAAACAGAA[A/G]TTCACCTGCACATCT	143279
rs138545622	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468263	GTACCAGCACCCCCC[A/G]GAGTTAGAGCATGCA	143279
rs138583425	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91495335	TTCTGACAGTATTGT[A/G]TTTCTAATACAATTA	143279
rs138606572	snp	G/T	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471057	ATTCCTGATGAAAAT[G/T]GATGCAAAAACCCCT	143279
rs138606624	snp	A/G	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433156	AAGATCTTTCCCTAG[A/G]TCAGAGTGGGTAACT	143279
rs138607470	snp	A/G	0.00438332	0.0466095	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91486553	CCTGAACCTAGAGGG[A/G]AACAGGAGCCCTATG	143279
rs138762222	in-del	-/TCTC	0.189576	0.242588	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496437	TTTCTACCTGCACAG[-/TCTC]TCCTCCTAATGCTAT	143279
rs138808828	snp	A/G	0.000134118	0.00818786	synonymous-codon, intron-variant, nc-transcript-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482987	TCAGTTTAATAACAC[A/G]TCTACGTATGTCATC	143279
rs138831745	snp	A/G	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91495727	TAGCTTATCAATAGC[A/G]TGTTTATATCCATAT	143279
rs138882537	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500834	CAAGTTTCTACAAAA[C/G]TGTAGAGATTTTACT	143279
rs138988222	snp	A/G	0.00478085	0.0486577	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420151	TTTATTATTCTATCA[A/G]TGTGTGAAAATGTCT	143279
rs139084796	snp	C/T	0.00517822	0.0506191	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410152	CGAGGGGGACTACCG[C/T]CGGCGCTCCCGACCC	143279
rs139103320	snp	A/T	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461948	TTTGTACATTTCTTT[A/T]TATTTTCAGAAATTT	143279
rs139123218	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415414	TAAGTGTTTATAACA[A/G]TAATAGCTACTTATT	143279
rs139201790	snp	C/G	0.0275645	0.114116	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468823	TGCTTATAGTCCCAG[C/G]TACTTGGGAGGCTTT	143279
rs139241648	in-del	-/TATGGT	0.0162398	0.0886349	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462024	ATTATGAAGGAATAG[-/TATGGT]TCAAATTTTACTAAG	143279
rs139289660	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481296	AGATTTTTTTTAAAG[C/T]AGGATTAATAAGATT	143279
rs139358344	snp	G/T	0.00398564	0.0444627	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444888	CATTCAGCGAACTTA[G/T]GAACACTGTGCTGAA	143279
rs139365240	snp	A/G	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467198	TTGCCACGGGCCTCC[A/G]GAATCCTGGCAACAG	143279
rs139385765	in-del	-/AC			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470974	TTCTGTGTGGCAGAG[-/AC]ACACACACACACACG	143279
rs139418126	snp	A/C	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91515296	CACCCAGATGGCCGC[A/C]AATCGTTTAGTCTAG	143279
rs139505974	snp	A/G	0.00279162	0.0372561	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91435747	TCCCTTGTGCTATAT[A/G]CTCGGTCTAGCAGCT	143279
rs139542139	snp	A/C	0.0138799	0.0821421	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440284	AGAGTTTTTAGCATG[A/C]ATGGGGTGTTGAATT	143279
rs139563239	in-del	-/A	0.221737	0.248397	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450680	AAACAGATTTACAAG[-/A]AAAAAAAAAACCATC	143279
rs139571543	snp	A/C	0.00517822	0.0506191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502818	TACTTCTAAACTTTC[A/C]CAATAATTATTATTA	143279
rs139586669	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91473453	CTTAAACTTTAAAAG[A/G]TATATTTTAGAGAGA	143279
rs139638633	snp	C/T	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91416149	ACAATTGGAGAAAAG[C/T]GGTCATTATAAATTG	143279
rs139653131	snp	C/T	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91479857	TAAATGAAAAGTGGA[C/T]CTCATTTTTATGTAC	143279
rs139653225	snp	A/G	0.00795532	0.062565	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91418052	GACTTTTTAATGATC[A/G]CCAATGAATGTGCCT	143279
rs139690402	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422161	TCTGTTCAGGATAGA[A/G]TCTATACTCTGTAGC	143279
rs139713115	snp	A/G	1.66985e-05	0.00288946	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491208	TAATCAGCAAAGTCT[A/G]GTGGATAAAGTATCT	143279
rs139739753	snp	A/C	0.0023933	0.0345097	intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91488819	GAAGAAATTTTATTG[A/C]CTATGCCCATCAAGG	143279
rs139759784	snp	C/T	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91430802	TGGGTTTCCTGAATA[C/T]AGTACACTGATGGGT	143279
rs139876186	snp	A/C	0.0115144	0.0749975	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497688	ATGAACTGTATATTC[A/C]TGAATGCACATGAAT	143279
rs139916017	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91435982	TTACTTCTGCTGTTA[G/T]GCCTTTAATTGTGAA	143279
rs139973089	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457551	ATACTAACATGCTAA[A/G]AATGATTCCATGCAG	143279
rs139985402	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91423129	TGAAAATAGGCTGAT[A/G]TGTTCAACACACGTA	143279
rs140079267	snp	G/T	0.0221141	0.102801	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512476	TCTGTCTCAAAACAC[G/T]TTGACAAAGCTCACC	143279
rs140090339	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452644	CATACTCAGCCCCCT[C/T]ACCATGTGATGCCCT	143279
rs140098027	snp	C/G	1.65455e-05	0.00287619	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512376	TCAGAAGGTTTTGGA[C/G]TTGAGTAACCTAGAA	143279
rs140186441	snp	C/G	0.00478085	0.0486577	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483933	CTGTAGGGCACATCA[C/G]AACCTTCTTGTTAGG	143279
rs140275903	snp	A/G	0.00557542	0.0525036	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457906	CTCTTACTCTTATTC[A/G]TCTCAGTGCTGCAAA	143279
rs140281991	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500083	TAACCCACCTGAAAG[C/T]TGAAAAAAACAAGAG	143279
rs140310907	snp	C/T	0.00795532	0.062565	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476582	CCAGGCAGGATATGG[C/T]GCAATGCCACCACCG	143279
rs140609807	snp	A/T	0.0023933	0.0345097	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470512	GAAACTAATGAGAAC[A/T]AAGATAAAACATACC	143279
rs140631266	snp	C/T	0.0298908	0.118541	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91506283	AAAATCAGAGCAGAA[C/T]TGAAGGAAATAGAGA	143279
rs140699115	snp	C/G	0.00103608	0.0227369	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425324	TTTCCACTTTCAGCA[C/G]TTTTATTTCAGCTGT	143279
rs140762242	snp	A/C	0.00557542	0.0525036	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91486284	TTTAAGTTCTGGGCA[A/C]CCTAGTCCCAGATGG	143279
rs140781458	snp	A/G	0.00557542	0.0525036	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426269	AATGTACATTACTTA[A/G]ATACTTCTAAGTGCC	143279
rs140817593	snp	A/C	0.0023933	0.0345097	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91475083	CTGCATATGACCATG[A/C]AAGTTTAATTGTATG	143279
rs140859695	snp	A/G	0.00358779	0.0422022	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91495230	CTGAAATTTGAGAAA[A/G]AACAGGTATGAACAT	143279
rs140867330	in-del	-/TGAA	0.0240643	0.107019	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464960	AACCTAACTGTATTT[-/TGAA]TGAATGAACACTATA	143279
rs140899600	in-del	-/AC/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458037	AAAAAAAAAAAAAAA[-/AC/C]CCCATGAAATCTCAA	143279
rs140911337	snp	C/G	0.0275645	0.114116	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91455211	AGTGTTCCTATTTCT[C/G]TACATCCTCTCCAGC	143279
rs140912661	in-del	-/TT	0.145642	0.227177	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91416906	GCACTCTCTGAACTC[-/TT]TGGGGCTGGTATATG	143279
rs140937176	in-del	-/AC/ACAC	0.343722	0.251152	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426567	TTTGCATACAAACAT[-/AC/ACAC]ACACACACACACACA	143279
rs140984260	snp	C/T	0.0329836	0.124112	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450155	GTAACCAGAATAGCA[C/T]AGTACTGGTACCAAA	143279
rs141076805	snp	G/T	0.0182019	0.0936463	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91453791	TCTATTTATAAGAAA[G/T]TTGCTTCAAATATAA	143279
rs141175665	in-del	-/A			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91510702	AGCAGAGCACTTTAG[-/A]AAAAAATATATTAAA	143279
rs141201903	snp	A/G	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498597	GAGCTCCAGGGACCC[A/G]CTGTGTATTATCTAG	143279
rs141320148	snp	A/G	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91454077	AACAAAAAAATCCAC[A/G]ATTAGGTATTGAAGT	143279
rs141342572	snp	A/G	0.0023933	0.0345097	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470740	AACCAGGAAGAAATG[A/G]AAACCCTAAACAGAC	143279
rs141348612	snp	A/C/G	0.000396085	0.0140682	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499139	AGTGTGTGTGCTTCA[A/C/G]ATGCCCTAATGGTGA	143279
rs141382383	snp	C/T	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422085	ATAGTGATTTTTTTC[C/T]AAAATACAGATATGA	143279
rs141407993	snp	A/T	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91454586	TGTCTTTTTTTTTTA[A/T]TACTTTAAGTTCTAG	143279
rs141441353	in-del	-/C	0.0368353	0.130617	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91423707	AGAGACTTCTTAATT[-/C]CTATGTGTATAGTGT	143279
rs141512971	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461560	GGGGGTTGTTTTGTT[C/T]TGTTTTGAGATGGAG	143279
rs141537605	snp	A/G	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412188	TTAATAACTGTAATG[A/G]AATTATGTGTTCATG	143279
rs141578219	snp	C/G	0.00795532	0.062565	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419312	AATTTAAGATTCAGT[C/G]TGTTCCTCAATAGAG	143279
rs141587418	snp	A/G	0.00438332	0.0466095	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471309	ACAACTAGGCATTGA[A/G]GGAACATGCCTCAAA	143279
rs141589394	snp	A/G	0.00358779	0.0422022	upstream-variant-2KB, intron-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409324	GTGGTGGAGGTGGGG[A/G]GTATTTTAATTTCAT	143279
rs141683229	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415172	TTCCAGATGAGGTCA[A/G]TAGCATTCCAAATTA	143279
rs141702891	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468031	CCACTCCTACTAGTA[A/C]CTTGCCCCAGCAGAT	143279
rs141811013	in-del	-/GG/GGG/GGGG			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420709	GAACAGAGACTGGCT[-/GG/GGG/GGGG]GTTTTTTGTGCCTCT	143279
rs141813198	snp	A/G	0.0123036	0.0774623	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471698	CAAATCAAGAACGCA[A/G]TTCCACTCACAATAG	143279
rs141854224	in-del	-/TG/TGTG/TGTGTGTGTG	0.407845	0.193868	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412668	GGATCTGTGGCAGAA[-/TG/TGTG/TGTGTGTGTG]TGTGTGTGTGTGTGT	143279
rs141970861	snp	C/T	0.0115144	0.0749975	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496162	ATGCATAATTCAGAA[C/T]TCATTTGTTGTCATG	143279
rs141995546	snp	C/T	0.00716266	0.059414	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500989	CCACTGCTGAACTTA[C/T]ATACTTTTATAAAAA	143279
rs141996197	snp	A/G	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91435093	TATAATCAACATTTT[A/G]TACATTTTAATAATA	143279
rs142029829	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445430	GTTTCAATATAAATA[A/G]TTTTTAATTAAATAA	143279
rs142073626	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91513788	GGCTATTTTCTTGCT[A/G]TGCTTCCTGCACCCA	143279
rs142174452	snp	A/G	0.00517822	0.0506191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410878	AAGAGAATGACCTGC[A/G]TCTTGAGTCGGCATG	143279
rs142211925	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458475	GAACTGGAATGGGTA[A/G]AACTGTTTTTTAAAA	143279
rs142330175	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91466724	ACACAAATGGTTACA[A/G]CAGCCAAAAATTAAT	143279
rs142335643	snp	C/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415677	CTCGACATTTGCGGT[C/G]ATAGGTAATAGGGAC	143279
rs142395000	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91469748	AGGAATGTAAAAAGG[A/C]TAAATGTCTACTTAA	143279
rs142427582	snp	C/G/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421031	TCAAACCTTTGCATT[C/G/T]TTCCCCCCCTCAGGC	143279
rs142434813	snp	C/G	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91411418	AAGTACTTTTTGAAA[C/G]TTTGCTTTGATATAT	143279
rs142437208	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91443976	ATGGCTTCTTATAGA[A/T]TATATTTGGTAATCT	143279
rs142473066	snp	A/G	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91424500	TCTGGAAATTGGAAC[A/G]TAGTATAAAAAGATC	143279
rs142488308	in-del	-/GGTTG			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437639	TTTTTTTTTTTTTTT[-/GGTTG]TTTTGTTTTTTTTGT	143279
rs142628720	snp	A/G	0.00318978	0.0398085	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464568	TAGATGTCAGCTGCC[A/G]AGACTGGCCAGGAGG	143279
rs142746349	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440317	ATTGAAGGACTTTTC[A/G]GTAGTTATTGAGAAA	143279
rs142831555	snp	C/T	0.00279162	0.0372561	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450590	AGAGTGAAGAGGCAG[C/T]CTACAGAATGAGAGA	143279
rs142842808	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91479250	AGCACATTCCTATTA[C/T]TGGTTTTTTATATAT	143279
rs142897056	snp	C/T	0.0244538	0.107838	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91429251	TCATGGTGGAGAAGC[C/T]TTTTGATGTGCTGCT	143279
rs142933341	snp	A/C	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91486727	AGTTCATTGCATTTT[A/C]TTTTTATTTCCAATT	143279
rs142994582	snp	A/G	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476163	GATGATACAGGAGAG[A/G]TAAGGAAAAACTTTA	143279
rs143008675	snp	A/G	0.000118274	0.00768916	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478150	AATTAACATATAAAC[A/G]TCACCTAATTTGGTA	143279
rs143018136	in-del	-/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91459272	GGAATGTGAAATGGT[-/C]ACAGCCACTCTGGAA	143279
rs143073026	snp	C/T	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491705	AAATTAGAGGTCTGA[C/T]CTACAGGGTATATTG	143279
rs143156010	snp	A/C	0.0275645	0.114116	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91480088	AGACTCAAAAAGATG[A/C]AACCCCTGTTACATC	143279
rs143184142	snp	C/T	0.0232847	0.105357	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499840	ACTATAGAAGTTGCT[C/T]TGGGGCAAAACCAAG	143279
rs143288851	snp	C/T	0.00358779	0.0422022	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91454086	ATCCACAATTAGGTA[C/T]TGAAGTCTCCAACTG	143279
rs143439131	snp	A/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457745	AAGTTTGGGAACAAG[A/T]CAAGGATGTCTGCTC	143279
rs143514405	snp	A/G	0.00517822	0.0506191	intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462702	ATGCATATTTGAAGG[A/G]CTAAGTGGGAATGAT	143279
rs143515247	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485056	TTCATTTGGAGCTAC[A/G]TTTATTTAAAATAGG	143279
rs143557737	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512916	GATTCTTCTCAGCAG[C/T]TGCTGAAAAGCATGT	143279
rs143598172	snp	C/T	0.021333	0.101051	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449546	AAATTTTGGCCAGGG[C/T]AATCAGGCAAGTGAG	143279
rs143657644	snp	G/T	0.00318978	0.0398085	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458757	AAATGGATAATGGAC[G/T]TAAATGTTAAATTAT	143279
rs143668915	snp	C/T	0.0023933	0.0345097	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419319	GATTCAGTCTGTTCC[C/T]CAATAGAGGTTGAAA	143279
rs143686203	snp	A/G	0.0271762	0.113356	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91427635	GTGTTTTTTGGCAGC[A/G]TAAATGTCTTCTTTT	143279
rs143763899	snp	C/T	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467360	GGGTTGCCCATCCCT[C/T]AAGGCTCACTGTGCT	143279
rs143774911	snp	A/G	0.0174175	0.0916809	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432637	GCACAGAATATCTTT[A/G]AAAGAAATGAAGCAA	143279
rs143802686	in-del	-/A			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91494401	GAGAATGGTGAGAAT[-/A]AAAAAGGCTAAATTG	143279
rs143873838	snp	C/G	0.0267878	0.112589	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421039	TTGCATTCTTCCCCC[C/G]CTCAGGCTTTTTTCC	143279
rs143892025	snp	C/G	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484267	TGAAGACTGAATATT[C/G]AAAGTCTTTAAAATG	143279
rs143927425	snp	C/T	1.66363e-05	0.00288407	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484524	TGTCCCAGAAGAGGT[C/T]CAAACAATTGGTAGA	143279
rs143930446	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91488331	TAGCAAGCAGACTGA[A/G]TTTAGGCAAATTGTA	143279
rs143944464	snp	A/G	0.00557542	0.0525036	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91513049	CAGCTTTTACAAATC[A/G]ATAAAGATGATTGTA	143279
rs144011570	snp	A/G	0.00874735	0.0655527	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487419	AAATTATTTGTATAG[A/G]CAATGTAAGTGGTTA	143279
rs144083028	snp	A/G	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91469248	CATTCAAATTCAGGA[A/G]ATTCAGAGAACCCCT	143279
rs144139704	snp	A/G	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460194	AAGGGAAGAAGCTCT[A/G]TATTAAGTATGCACA	143279
rs144210928	snp	C/T	0.0185938	0.0946107	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440459	ATAAGCTTTTTGATG[C/T]GCTGCTACATTTGGT	143279
rs144224897	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445853	ACGGTGCACTCCGGC[A/C]CAGATACTACACTTT	143279
rs144377481	snp	A/C	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502300	TGCCTTTCTTCCTCC[A/C]TGCTTTCAAGTTGTT	143279
rs144418321	snp	G/T	0.000307953	0.0124049	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499072	TTATACTGACTTCCT[G/T]CTGAACAAATCCATC	143279
rs144484208	snp	G/T	0.00636936	0.0560724	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91456704	TTCAGTATGATATTG[G/T]CTGTGGGTTTGTCAT	143279
rs144529733	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91434377	GCTCATTTATTATTA[C/T]CTGGCTGGTACTCAC	143279
rs144557375	snp	C/G	0.00318978	0.0398085	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91435778	TCATGTCCTTAAATT[C/G]CAGAAAATTTTCTTG	143279
rs144638484	snp	C/G	0.00478085	0.0486577	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91469797	TTGTATAAGAAGAAA[C/G]ACCAAACTATATGCT	143279
rs144676392	snp	C/G	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91475204	TGTCAAGAGAAAGGA[C/G]TTAGGAAGGCCTTGT	143279
rs144768243	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91418920	TATCTCAGGAAGCTA[C/T]TCATTCTTTTGAAAA	143279
rs144798104	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91453982	AATCACCCAAAATAT[A/G]TAGTCATCACAAGTG	143279
rs144829494	snp	A/C	0.00318978	0.0398085	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451054	ataaatcattctgct[A/C]taaagacacatgcac	143279
rs144840689	snp	C/T	0.000347777	0.0131821	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496351	CAATGTTACCGTGGA[C/T]GACTTATGTCAAATT	143279
rs144846347	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502368	ACACAGTTTAATGTT[A/G]ACTTCCTCTGTAAAG	143279
rs145033788	snp	A/G	0.0267878	0.112589	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498763	TTTTATAGTTTATGT[A/G]TTTAGAAGGAAGGGG	143279
rs145070400	snp	A/C	0.188	0.24219	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410255	CGCGGGGCTGGCGCG[A/C]GCGGGGGCGGCCTCG	143279
rs145074472	snp	A/G	0.00318978	0.0398085	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91453717	AAAATTACATTAAAT[A/G]TAAATGGTCTAAATA	143279
rs145092388	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470946	GAGGCCAGCATCATC[C/T]TGATATCATCTTTTC	143279
rs145123858	snp	C/T	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503082	TAAGAATGGTAATTC[C/T]ATTAAAAGGTGGGCA	143279
rs145162657	snp	G/T	0.00318978	0.0398085	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444889	ATTCAGCGAACTTAT[G/T]AACACTGTGCTGAAC	143279
rs145217168	snp	A/G	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422836	TGTTGAATAACTGTT[A/G]ATTGAATTCTTAATT	143279
rs145217749	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91423437	TTAACCCAGACATTA[C/T]TGAGCTGAAATCTGG	143279
rs145295482	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91489602	TATTAGTTATTTCCA[A/G]TGTGACAGCTGCCCA	143279
rs145417431	snp	A/G	0.00358779	0.0422022	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500673	GGAACAGCAGACAGT[A/G]TGGTTCATTTATTTG	143279
rs145436805	snp	C/T	0.00517822	0.0506191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445978	TGAGCAGACACCGAA[C/T]TTGCTGCAGGAATTT	143279
rs145689336	snp	A/T	0.0263992	0.111815	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509276	ACTTAAAGTATAATT[A/T]AAAAAAATAAATTTA	143279
rs145729205	snp	G/T	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91475612	AGTACAGATAATTCT[G/T]GAGAGCTTTCACTAT	143279
rs145770948	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458300	AGTAAGTGTAAAGGC[A/G]TACTGTGTTCATGGA	143279
rs145797571	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437065	CTGAGAGATTACGTG[A/G]TTTCTGTTTATACAT	143279
rs145818667	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425501	GCATTGTTCTGATAG[A/G]TCTAGTTAATACAAC	143279
rs145963596	snp	A/G	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468130	CACTACCCCAGTCAA[A/G]TGTTTTGTCTGACAC	143279
rs146085273	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91495694	TCAAGTTTTACTGTT[A/G]GAAATTACCTATCCT	143279
rs146153729	snp	C/T	0.0023933	0.0345097	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432849	GCATACTGTGATCTT[C/T]GTCACCCTGAAATAG	143279
rs146175460	snp	C/T	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468662	ATCTAAAGAATACAA[C/T]AAAATAATACAGGAG	143279
rs146185708	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471505	AAATAGAAGGCACCA[A/T]AATAGGACGAGAGGA	143279
rs146186055	snp	A/G	0.00517822	0.0506191	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410151	ACGAGGGGGACTACC[A/G]CCGGCGCTCCCGACC	143279
rs146212536	snp	A/G	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415266	AGCTAGGTATTTGGA[A/G]CAATCTTGTATGAAA	143279
rs146233911	snp	A/T	0.0119091	0.0762411	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438316	CAACTGCCACTTACG[A/T]GTGAGAACATGCAGT	143279
rs146293559	snp	A/G	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496472	CTTACTTTTAAATAT[A/G]GTTTCCTTCTACCTT	143279
rs146304491	snp	A/G	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501091	TTCAGGATATTATGT[A/G]TGCTTAAGGAAAGTC	143279
rs146331559	snp	C/G	0.0260105	0.111035	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440268	AATACCTAGTTTATT[C/G]AGAGTTTTTAGCATG	143279
rs146413659	snp	A/G	0.00517822	0.0506191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457259	CACCATTTCTGTACA[A/G]TCTCTACCAGAAAAT	143279
rs146468869	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91411527	CCTACTTGCGGTTCA[C/T]TTCTTAAAACCTCCC	143279
rs146474503	snp	A/T	0.185472	0.241529	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91505775	ACACCAAGCAGACCT[A/T]ATAGACATCTACAGA	143279
rs146523990	in-del	-/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420280	AAGCTTTTATGATTA[-/C]AAAAAAAAAAAAAAA	143279
rs146615071	snp	A/G	0.000329826	0.0128376	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499105	TAAGCAGTTTGCTGC[A/G]TTTTATTATGGATTT	143279
rs146618495	snp	A/G	0.0681886	0.171594	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91430886	CTATTTACATTTAAA[A/G]TTAATATCATTATGT	143279
rs146628901	snp	A/T	0.0126979	0.078662	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91435920	ATTTCTCTTCTCTTT[A/T]GCTTTATGATTTAGG	143279
rs146740810	snp	A/G	0.0850919	0.187897	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457902	TTTGCTCTTACTCTT[A/G]TTCATCTCAGTGCTG	143279
rs146752407	snp	G/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91463073	TTGAACAATGCGAGG[G/T]TTAGGGGCGCTAACC	143279
rs146778781	snp	A/G	0.00438332	0.0466095	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91430536	TTTGTAGGTCACTCA[A/G]GACTTGTTTTATGAA	143279
rs146856368	in-del	-/GGGG	0.139225	0.224118	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451008	AGCAATCCCGTTACT[-/GGGG]GGGTTTTATCCTTTT	143279
rs146862261	snp	A/C	0.000205782	0.0101414	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91484290	TTAAAATGTTTGTTA[A/C]TAACTTTATAGTAAT	143279
rs146873555	snp	C/T	0.00358779	0.0422022	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91424734	CCCAAGTGCTTAGCA[C/T]TACTTCTAAAAAAAA	143279
rs146873876	snp	G/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91488342	CTGAGTTTAGGCAAA[G/T]TGTAGAGCAGTATGA	143279
rs146913627	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467197	CTTGCCACGGGCCTC[C/T]GGAATCCTGGCAACA	143279
rs146922444	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91494732	ATTCTAGTATCTGCA[A/G]TAATCATTTGTTGAA	143279
rs146932488	snp	A/C/G	0.0115144	0.0749975	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431709	CTTCACGTGGTTCTC[A/C/G]AGCCTTGGCTTTCAG	143279
rs146955629	snp	C/T	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437354	CTTTTTCAGGTGGCT[C/T]TTGGCATCCTCACAG	143279
rs147008685	snp	C/T	0.00755907	0.0610114	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91486966	TTCACTGTAGTCACT[C/T]TGAATGGCAATCTAA	143279
rs147060057	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91465693	TATTGCTATGATCCC[A/C]TGATTTTTCTTTTTT	143279
rs147186057	snp	A/C	0.00835141	0.0640778	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422986	ACATGAGAAGTTTCC[A/C]TAAAGTACACTTAGT	143279
rs147291583	snp	G/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451394	GGACCAGGGGAGGGA[G/T]AGCATTAGGAGAAAT	143279
rs147301911	snp	G/T	0.0146672	0.084371	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91455134	GTTCGAGATCCTTGA[G/T]GAATCGCCACACTGT	143279
rs147397267	snp	A/T	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91474884	AGGCAACAATTGAGG[A/T]CTTAATGATGAAAAT	143279
rs147406640	snp	C/G	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91479600	TTACCTAACCATTCT[C/G]CAAGAATGGTTGTTT	143279
rs147487868	in-del	-/G	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91494960	ATGAAATTGCTCATT[-/G]TTTTTTTTGCAATAG	143279
rs147497801	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502810	GGTGACATTACTTCT[A/G]AACTTTCCCAATAAT	143279
rs147521028	snp	C/T	0.0142736	0.0832652	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512184	TTGAATGTGTGTGTC[C/T]TGGTATTTTTTAAAG	143279
rs147552421	snp	G/T	0.00727415	0.0598679	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498844	TTATATCAACCATAT[G/T]AATATGTGTAATGGC	143279
rs147689382	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91469487	TTCCAACCAAGAATT[G/T]CATATACAGCCAAAC	143279
rs147783278	snp	C/T	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493223	TATATATTTAATATA[C/T]ATATTTATATTTGCT	143279
rs147793304	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498399	GGGTTCAGAGTACTC[C/T]CTAGGCAATTACATA	143279
rs147887060	snp	A/G	0.0244538	0.107838	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91411655	TGTCTGAGGGCCCTG[A/G]TAACTGGAAATTGTT	143279
rs147896982	snp	C/T	0.0103295	0.0711199	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419284	GGTAGAAAAATATGA[C/T]GAAGAAATTGGAAAT	143279
rs147979310	snp	A/G	0.00478085	0.0486577	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471567	ACCTAGAAAACCCCA[A/G]ACCCTCTGCCCAAAA	143279
rs148048715	snp	C/T	1.64887e-05	0.00287125	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460489	ACATCTATGGATGCA[C/T]CATCATCCGAAATGA	143279
rs148094226	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509510	ACACATGCATGCATA[A/T]GTTCATTGTTCACTG	143279
rs148128977	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467479	GTGTCCCCCTGACTG[C/T]TGGCCTCTCCCAGGG	143279
rs148182687	snp	A/G	0.00478085	0.0486577	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421562	AATTTGTGTTGGGCC[A/G]CATTCAAAGCCATCC	143279
rs148254287	snp	A/G	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499912	AATATGTTTGTTGTC[A/G]AAAATACCTTTGAAA	143279
rs148277411	snp	C/T	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438728	GTTTCTCCACATCCT[C/T]TCCAGCATTTGTTGT	143279
rs148307076	snp	A/G	0.00557542	0.0525036	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91454565	ATACGTTAGAAAGGT[A/G]GAAAGTGTCTTTTTT	143279
rs148457995	in-del	-/AA	0.139564	0.224285	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91418116	AATTCAGCTGAATTG[-/AA]AAAGTCAGTCTGAAA	143279
rs148473428	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464045	GGCAATCTAGTCCTC[A/G]AGGGATCCAGGCTGA	143279
rs148535574	snp	A/G	0.0204879	0.099117	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487543	AAAGAAATTATACAC[A/G]TACAATCATTTTGTA	143279
rs148586448	snp	C/T	0.0267878	0.112589	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91496792	TTATTATGTAAAATA[C/T]AGAAAATCATTCTAA	143279
rs148629500	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91513219	TATTAGAAAAGAAAT[A/C]AGACCTAAATAATCA	143279
rs148663877	snp	A/C	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91469401	TCAGGCTAACAGCAG[A/C]CCTTTGAGCAGAAAC	143279
rs148779179	snp	C/T	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502307	CTTCCTCCATGCTTT[C/T]AAGTTGTTCCCTTTA	143279
rs148802398	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91443832	AAGAGTTTATTAAAT[C/G]TACTTCAGTGTTACA	143279
rs148821829	snp	C/T	4.21381e-05	0.00458991	synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425400	TCTTGTTTTCCCTAA[C/T]ATCAAGAATGGTAAA	143279
rs148853604	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437093	CATGTTCCAGTATCT[A/G]TTGAATATATAATAA	143279
rs148895234	snp	A/G	0.0197687	0.0974348	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91504885	CCAGAGAGAAAGGTC[A/G]GTTTACCCTCAAAGA	143279
rs148927756	snp	A/G	0.00914312	0.0669923	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91475679	TGGCCCAAACGAGAT[A/G]TTTTAAATAAAGTCA	143279
rs148978365	in-del	-/A	0.0115144	0.0749975	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91414684	TTAAGCTGGCTGGCC[-/A]TTGAAAAATGATAGG	143279
rs149060975	snp	G/T	0.00438332	0.0466095	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91489879	AGCAAATTGCTGCAT[G/T]TATTTAAAATGTCTG	143279
rs149090351	in-del	-/C	0.0182019	0.0936463	intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91408057	GCTATAATTCTACAG[-/C]TTTCCAGCAGGCCCC	143279
rs149123459	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499705	CATAGGATACCTTTC[A/G]GTCACCCCAGCTACC	143279
rs149137847	snp	A/G	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91423772	ATTTCTTTAAAAAGT[A/G]AATTTAAAGTGTAGC	143279
rs149205373	in-del	-/TGAG	0.00478085	0.0486577	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512580	CACACAGAAATCGCT[-/TGAG]TGAGGAAAAGTCCAC	143279
rs149238846	snp	A/C	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426733	GCCTACAAGTTTTTG[A/C]TTGGCCATATTGACT	143279
rs149280520	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464794	GACACAGCCCACCTC[A/C]CAGCCACTCAGCCTA	143279
rs149283325	snp	C/T	0.0271762	0.113356	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91456638	AGTGGTGAGAGAGGG[C/T]ATCCCTGTCTTGTGC	143279
rs149422678	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467309	TGTGGCGCCCAGATG[A/G]TTTGGTATGGGAACA	143279
rs149443990	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451041	CACCCAAAGGATGAT[A/G]AATCATTCTGCTATA	143279
rs149453116	snp	A/C	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478023	TACTCTTACTGTAAT[A/C]TTATGTCATTGATGC	143279
rs149471229	snp	A/G	0.000313188	0.0125098	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462099	TGAATTTGCAGAAAG[A/G]TGCCACTGCCTCATT	143279
rs149600929	snp	C/T	0.0325976	0.123435	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91495489	TATGATCCTATAAAA[C/T]GAATTACTTCCTTAA	143279
rs149633817	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91414191	ATAGGGTACCAGTAC[A/G]TTGGGTTCAAGAAAG	143279
rs149651981	snp	C/T	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502245	TTTCTTTCTATGCTT[C/T]AGTCAACAGGCTGTT	143279
rs149699666	snp	A/C	0.00478085	0.0486577	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498338	CCTGATAAAGTAGAC[A/C]TGTGTAGATGAGCAG	143279
rs149760758	snp	A/G	0.000149602	0.00864747	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491239	CGAAGACAGAGACCT[A/G]ATATGAATATATTAT	143279
rs149793759	in-del	-/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91413794	GAAATGGCAGTGGCA[-/G]GTGGTTCCAGTTAGA	143279
rs149946893	snp	C/T	0.00636936	0.0560724	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91469020	AAAGAATTTCAGAGC[C/T]CAAAGACTGATTCTC	143279
rs149964627	snp	G/T	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452907	ATGAAGAAAAACTAA[G/T]AATTTGTTGCCACTA	143279
rs149999458	snp	A/G	0.00279162	0.0372561	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91423359	AATGTATTAAAGTAG[A/G]TACTGTAGTAGTAGG	143279
rs150041285	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91488822	GAAATTTTATTGCCT[A/G]TGCCCATCAAGGGAA	143279
rs150088551	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91486509	TTAGGGTTTTAATCC[C/T]AGGATCCTGTCAACC	143279
rs150111508	snp	C/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426606	CACACACCCCTCCGT[C/G]ACGCCAATATTGCCC	143279
rs150143763	snp	C/T	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91495233	AAATTTGAGAAAGAA[C/T]AGGTATGAACATTGA	143279
rs150183845	snp	C/T	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91510136	TCTCCCAGTGCCTCT[C/T]AGAATAAAGTCCATG	143279
rs150229000	snp	A/G	0.00438332	0.0466095	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458177	CTAAAATAAAAATGC[A/G]TATCATTTGTAATCA	143279
rs150309016	in-del	-/AAGA	0.00874735	0.0655527	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91479381	TGTCTCAAAAAAAAG[-/AAGA]AAGTAAAAAATGTTT	143279
rs150322963	snp	A/G	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476760	AGAGGAGTGAGAACC[A/G]TCTTCTTGAAGTTCT	143279
rs150350607	snp	G/T	0.0138799	0.0821421	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438947	TTTTCTTGCAAATTT[G/T]TTGAAGTTCCTTGTA	143279
rs150489682	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91413358	CTAGTGAGGAGGTGC[A/C]TAACACAGTGGTTTC	143279
rs150503265	in-del	-/T	0.0256215	0.110247	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91417383	TCATTTACTTTTTTC[-/T]TTTTTTTTATTACAC	143279
rs150582936	snp	A/G	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471893	ATACTGCCCAAAGCA[A/G]TTTACAGTTGCAGTG	143279
rs150639591	snp	C/T	1.65578e-05	0.00287726	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487738	CAAAAAAAATCATTA[C/T]TCAGAGAGACTCAGA	143279
rs150659009	snp	A/G	0.00755907	0.0610114	intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91407741	ACCCTGCCAAACCCT[A/G]TTCCCCATAGGTATA	143279
rs150889664	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444698	TTAAAATATAATTCA[A/G]AAAGAGAAAATCAAT	143279
rs150961470	snp	G/T	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485805	ATGCATGATCTAATA[G/T]ATTGATCACACACAG	143279
rs150971617	snp	A/G	0.00438332	0.0466095	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464901	ATACAGATATGAGGG[A/G]AAAAACCCTAAATGG	143279
rs151024853	snp	A/G	0.00318978	0.0398085	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419447	AAATATCTTGAGATT[A/G]TTTTATATTATAATC	143279
rs151121240	snp	A/G	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476273	GTTGCAGGCAAATTG[A/G]TAGAATTTACATAGG	143279
rs151130208	snp	G/T	0.0174175	0.0916809	intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91515148	TGTCCACATACCTCA[G/T]GCTTAAGGAAGGAAG	143279
rs151147408	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450050	TTTCATATAGAACCA[A/G]AAAAGAGCCCATATA	143279
rs151235089	snp	G/T	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91469970	ACAACAATCAAAAAA[G/T]ACAAGAGCATTACAT	143279
rs180675992	snp	A/C	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91423086	CATCTATAAAAGTAG[A/C]GATTACATCAGCCAC	143279
rs180676078	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477206	AAAAAAAAAAAACCC[C/T]TGCGGGTCCAATGCA	143279
rs180677558	snp	C/T	0.0240643	0.107019	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450076	ATATAGTCAAGACAA[C/T]CCTAAGCAAAAAGAA	143279
rs180682097	snp	A/C	0.0236746	0.106192	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503604	CCACGAGATTATATC[A/C]CGCACTTGGCTCGGA	143279
rs180687694	snp	C/T	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467981	ACCACACCACCACTG[C/T]TGCCAGCTCAAGAGC	143279
rs180698156	snp	C/T	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91411941	AAATGTATGTACTTA[C/T]AGAAACAGTTAAATG	143279
rs180699892	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91435265	TGAGTCCTGAGAAGC[A/C]AAGGACACCTCTTGG	143279
rs180710624	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91456483	GATTTTGGGCTGAGA[C/T]GATGGGTTTTTCTAG	143279
rs180751593	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493650	ATTAGATTTTCAGTA[A/G]TCTTCATTATGTGTA	143279
rs180921373	snp	A/C	0.0433465	0.140692	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431018	TGCAGCGGCTGGTAC[A/C]GGTTGTGCCTTTCCA	143279
rs180933441	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91472673	CAAAAGAAGACATAC[A/G]TGTGTCCAACCAGCA	143279
rs180937030	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91514969	TGAAATGTATATCCA[A/G]TATTTGAAAGATCAC	143279
rs180965332	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461680	CAGCCTCCTGAGTAG[C/T]TGGGATTACAGGTGC	143279
rs180965657	snp	C/G	0.0023933	0.0345097	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451957	AAGATATTAATCATT[C/G]TGTTGTTTTAGAAGG	143279
rs180969852	snp	A/C	0.00478085	0.0486577	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419108	CTCCTTTTTTCAAGG[A/C]TTGGGTTAGAATGTG	143279
rs180975254	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91488221	GTAACAAAAAGTGTG[C/T]CTTGGAGAACTGAGA	143279
rs181153739	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457433	AAAATATTAGCAAAT[A/G]AAATTCAGCAATATG	143279
rs181167877	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91478520	TGTAAAGTTTTTTCT[A/G]TGCAGATATATATGC	143279
rs181198298	snp	C/T	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91436721	TATTTTTGCCTTCCC[C/T]GTTATATTCCCAGTT	143279
rs181199661	snp	A/G	0.00517822	0.0506191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492726	AAAGTAAACATTTAT[A/G]AGGAAACATCCATAT	143279
rs181208413	snp	C/T	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422489	AATTTGGCATTTGTT[C/T]GCACTATTATTAAGA	143279
rs181251042	snp	A/T	0.00636936	0.0560724	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503960	GCCGCCTCAAGTGGG[A/T]CCCTGACACCTGACC	143279
rs181270494	snp	A/G	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91467030	GCAGATCTTCAGAGG[A/G]AAGGCATTGAGATTG	143279
rs181317062	snp	C/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449691	AGCAACTTCAGCAAA[C/G]TCTCAGGATACAAAA	143279
rs181371951	snp	C/T	0.000150081	0.0086613	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461215	TTTATCTGAATAATA[C/T]TTCTATATGTATATA	143279
rs181374874	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487883	TAGCATAATCAGGAA[C/T]GTTAAAAGCAAAATT	143279
rs181402548	snp	A/G	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91418434	TATATGATCAATTGC[A/G]TTGATTTTTTTTTGT	143279
rs181402837	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438907	GTTCATATCCTTTGC[C/G]CACTTTTTGATGGAG	143279
rs181609964	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422094	TTTTTCTAAAATACA[A/G]ATATGATCATGTCAT	143279
rs181620964	snp	C/T	0.00199481	0.0315187	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91513991	AAAATCTTGGAAAGC[C/T]TAAGAGAGTTAAAGG	143279
rs181791278	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91435820	TGATGATTTTCTCTC[C/G]TCTGTATTTTCTATC	143279
rs181857165	snp	A/G	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477539	GAGGAAGAGAAAGGA[A/G]TGCTATATTAAATAT	143279
rs181890621	snp	A/C	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91473497	GAGATATAAGAAAGA[A/C]TGATGAAAAAGAAAT	143279
rs181897888	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91499588	CTTTTACCCTTAGCA[A/G]GTAGTTTATCTCTAG	143279
rs181914225	snp	G/T	0.0244538	0.107838	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431591	TTTCTTTTTATTCTT[G/T]TTTCTCTAAACTTCC	143279
rs181915783	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91452302	ACAAACCTCATTCAG[A/G]AGAAATCCAAAGAAA	143279
rs181999301	snp	C/T	0.0271762	0.113356	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91417611	ACGAGTGAGAACATG[C/T]GGTGTTTGGTTTTTT	143279
rs182025424	snp	A/T	0.0279526	0.114869	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412632	ATTATTTATTTTTTA[A/T]AAAAAAAAACAATTT	143279
rs182050816	snp	G/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91456955	CTAGGAAGACTGACA[G/T]AAAAAGGTAGATTGT	143279
rs182081675	snp	C/T	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91508846	TTATTGCGGTATTAT[C/T]CACAATAGCAAAGAC	143279
rs182084837	snp	A/G	1.66488e-05	0.00288515	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460586	TTTCAGCTATTATAT[A/G]TAAATGTATAGTCAT	143279
rs182101810	snp	A/T	0.00398564	0.0444627	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512514	AAATATTAAGTTTTT[A/T]AAAAATCAAATATGA	143279
rs182110963	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457899	ATGTTTGCTCTTACT[C/T]TTATTCATCTCAGTG	143279
rs182112902	snp	G/T	0.00279162	0.0372561	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91425170	ATACGTTTTTATCTA[G/T]TATCTACTCGTCATC	143279
rs182113664	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91481553	TTTTCACTTCACTAT[C/G]TATTTTTCAATAACT	143279
rs182115596	snp	G/T	0.00398564	0.0444627	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450817	ATCAAACCACAATGA[G/T]ATACCATCTCATGCC	143279
rs182122402	snp	G/T	0.00358779	0.0422022	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503756	GCAGCCAGGAAGCTC[G/T]AACTGGGTGGAACCC	143279
rs182284682	snp	A/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91454303	GAAATTTTGAAGAAT[A/T]GAGATAATGTAAAGT	143279
rs182297759	snp	A/G	0.00478085	0.0486577	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438131	ATACATGTGCAGAAC[A/G]TGCAAGTTTGTTTCA	143279
rs182303881	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91408034	AGCACACCACGAGTT[C/T]CCCCAGAGCTATAAT	143279
rs182311481	snp	A/G	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432337	TTAGGGAAACTGCAA[A/G]AACCCAGCGTGGGTT	143279
rs182370748	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91413703	AGTTTGTGGAGCAGC[A/G]TTTGAAATGGACTTG	143279
rs182387140	snp	A/C	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91486911	GTCACAGTTGTACCA[A/C]CTGACTATGCTCAGA	143279
rs182438642	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497536	GGCTGGTCTTGAACT[C/T]CTGACCTTGTGATCT	143279
rs182477076	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490443	TTTGATACATGTTGA[A/C]AAGTCACTTTTGTAA	143279
rs182509586	snp	A/C	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91413295	GAAAGGGCAGCCCTG[A/C]AGTGTTTTATCCTAA	143279
rs182665878	snp	A/G	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470758	ACCCTAAACAGACCA[A/G]TAATGAGCTCTGAAA	143279
rs182681069	snp	A/C	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91474987	AGGGAACACAATTGG[A/C]AAATTCAGAAATAAG	143279
rs182694490	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91436966	TTAAAGTGGAATTTC[A/G]GGAGGAATTAAAATA	143279
rs182900799	snp	C/T	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91489749	GTTAATAGCATTTAG[C/T]GTTGTATATAGGAGA	143279
rs182930995	snp	C/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91443816	GGTGCTGATGACACA[C/G]AAGAGTTTATTAAAT	143279
rs182933089	snp	C/T	0.0271762	0.113356	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420566	GCACTCCAGCCTGGG[C/T]GACAGAGCAAGACTA	143279
rs182945206	snp	A/T			intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91463756	AACATTACACATCCA[A/T]CAAAATTAATAAAAT	143279
rs182952832	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91424410	AACTCTTCCTCTACT[A/G]TGAAAGTGAAGACGT	143279
rs182968640	snp	A/G	0.00557542	0.0525036	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501732	CTTTTCTAGGGGGTT[A/G]GGGGATACTATAATT	143279
rs183131205	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91494208	AGTATAAAAGGGGTG[A/G]GGGGGAATTCTTAAT	143279
rs183143982	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91423661	TCTGTGAAATGAAGG[A/G]GTTAACTAATTTCTA	143279
rs183159578	snp	C/T	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450289	AAAGGATTCCCTATT[C/T]AATAAATGGTGCTGG	143279
rs183161147	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468635	GGAGAAAGTAGAAGC[C/T]CAATATAAGGAATCT	143279
rs183211704	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432852	TACTGTGATCTTTGT[C/T]ACCCTGAAATAGCCA	143279
rs183237290	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91407293	TTCAAACTCCTGACC[C/T]CAAGTGAGCCACCTG	143279
rs183244897	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91453787	GTTTTCTATTTATAA[A/G]AAATTTGCTTCAAAT	143279
rs183251875	snp	C/T	0.00159617	0.0282053	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450555	TAAAGAGCTTCTAAA[C/T]AGTAAAAGAAACTAT	143279
rs183274238	snp	A/G	0.0482946	0.147699	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91454913	CTCATCCTTTTTTAT[A/G]GCTGCATAGTATTCC	143279
rs183275924	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476029	TCTAGTTGATACAGT[C/T]CTTCAGAATTGGCCT	143279
rs183283309	snp	C/T	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502628	TATATAATTAAATTT[C/T]TAAACAAAATTTACA	143279
rs183304586	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91495525	TTATATAATAATTGA[C/G]TGTTGAAATACTATG	143279
rs183320969	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91500236	TGCTGGTTTTTGGAG[A/G]AGAGTAATTTGGATT	143279
rs183480059	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431931	CTGGTGAGGAACTGC[A/G]AAGTTGGGGTATTTG	143279
rs183537878	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437348	TATGGCCTTTTTCAG[A/G]TGGCTCTTGGCATCC	143279
rs183549025	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91474334	TCACTGGTTAGAAGA[A/G]ACTATCACTTTAGAT	143279
rs183565282	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482889	TTCCTGAATTTACCA[C/T]GTACTTATTAAGCTT	143279
rs183722534	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485656	ACTATAGGTTACACA[A/G]GTTCTATTTTGCTAT	143279
rs183728999	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91511317	TGACACCAAAAGGAT[C/T]CAGAAGATAATTTTT	143279
rs183782385	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458472	GAAGAACTGGAATGG[A/G]TAAAACTGTTTTTTA	143279
rs183804584	snp	A/G	0.00199481	0.0315187	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91414019	ATTAGTTACTGATGT[A/G]TTACACATGTTTAAA	143279
rs183827476	snp	C/G			intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462844	GACATCTTTTCAATC[C/G]ATAAGCATACTGTAT	143279
rs183841087	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509186	GCTAGATGACGGGTT[A/T]GTGGGTGCAGCACAC	143279
rs183867907	snp	A/C	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91419705	ATATTTTGAGTATTT[A/C]TTTCCCTCAAAGAAT	143279
rs183897394	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91411090	TGTCAGTGTAGTGGG[A/G]GGTAGATGCATCAGT	143279
rs183921134	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91515209	GTTATGGGTGATTAA[G/T]GAAAGAAAATAGGTA	143279
rs183963001	snp	C/T	0.00358779	0.0422022	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91434085	GTAAAAAGTACATCT[C/T]TAAAATCTAATGAAT	143279
rs183963991	snp	A/C	0.00636936	0.0560724	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91456158	TGAATCTATAAATTA[A/C]CTTGGGCAGTATGGC	143279
rs183970127	snp	A/G	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476903	CTGCGGGTCCGGGCC[A/G]GGCGCGGTGGCTCAT	143279
rs184016815	snp	G/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91440366	TCGGTTCTTTTTAAG[G/T]GATAGGTTACATTTA	143279
rs184023063	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91408834	AAATAGGTGGCAACA[A/G]CAACTATATTAAAGT	143279
rs184025062	snp	C/T	0.00159617	0.0282053	intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91489371	ACACAAGGACAATCT[C/T]ACAAATAGTCAGTGT	143279
rs184168029	snp	C/T	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91416400	TGACAGATCACATAA[C/T]CTGAAGGCAGTCTAA	143279
rs184177361	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485364	TTCAAAAGAATGACT[A/G]GAGTTTAAGTTTATA	143279
rs184187061	snp	A/G	0.000798403	0.0199641	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509819	TAAAAGAAACTGCCT[A/G]TCAGGTACTTACTTA	143279
rs184203800	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415382	GAATAAACTACAGAT[A/G]TTACAAATATACAAA	143279
rs184204006	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437683	ATATTTTCTTATACT[C/G]TGTTTAAGGTAGAAA	143279
rs184212872	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458813	GATCTTTGGGCTCTA[A/G]AACTAGAAAATAGTT	143279
rs184220292	snp	G/T	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91422101	AAAATACAGATATGA[G/T]CATGTCATATCTTGC	143279
rs184274673	snp	A/G	0.0023933	0.0345097	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449475	AAGCATTCCCTTTAA[A/G]AACTGACAGAAGACA	143279
rs184276668	snp	C/T	0.0023933	0.0345097	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91466841	TGAGATACCAAGTCA[C/T]AAAAAGACATGGAGA	143279
rs184286758	snp	A/G	0.000399281	0.0141238	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91492432	GGATATGGGTGGTTT[A/G]ACTAAAGAATGGTTC	143279
rs184309277	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437869	TTGAATAGTTGTAGA[G/T]ATGAAAGTGATCTAA	143279
rs184444840	snp	A/G	0.00119737	0.0244387	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91426604	CACACACACCCCTCC[A/G]TCACGCCAATATTGC	143279
rs184466545	snp	C/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445716	GACTGGTTAGACAGT[C/G]GGTGCAGACTGTGGG	143279
rs184489983	snp	C/G/T	0.00199529	0.0315338	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451369	CACACTGGGGCCTTT[C/G/T]GGTGGATTGGGACCA	143279
rs184493925	snp	G/T	0.029116	0.117091	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91417619	GAACATGCGGTGTTT[G/T]GTTTTTTGTCCTTGT	143279
rs184505257	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471198	AATGTGATTCATCAC[A/G]TAACAGAACTAAACA	143279
rs184509570	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497992	ATTTTGTGCCCTGGA[A/G]AATACATGTCAAATA	143279
rs184588923	snp	G/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420979	TATAAGGGAACATTA[G/T]ATGGCAGCCATGGTA	143279
rs184641171	snp	A/G	0.00755907	0.0610114	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503475	CTCGGGAAGCGCAAG[A/G]GGTCAGGGAGTTCCC	143279
rs184662173	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91464973	TTTTGAATGAACACT[A/G]TAACCATATTTTCCA	143279
rs184745556	snp	A/C	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421909	TATGCTTCAGACTTA[A/C]ACCTGAAATCGCTGT	143279
rs184775831	snp	A/T	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91430372	TGATTTGGGGTGGAG[A/T]GTTCTGTAGATGTCT	143279
rs184787269	snp	C/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471773	GTAAGAGAGCATTAA[C/T]AATGAGAATTACAAA	143279
rs184895689	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451768	TGGTAGAGCCAAGGA[C/T]AGATGCTTGAATAGG	143279
rs184939487	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91456710	ATGATATTGGCTGTG[A/G]GTTTGTCATAAATAG	143279
rs184959563	snp	A/G	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91498737	AATACAAATATTGCA[A/G]GAGCTTAGCCTTTTA	143279
rs184991712	snp	C/T	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91477447	TTGGTTTTTCTCCTG[C/T]AGCTTTTGTTGCTCA	143279
rs184999913	snp	A/G	0.00636936	0.0560724	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91503642	ACCCCACGGAGTCTC[A/G]CTGATGGCTAGCGCA	143279
rs185034048	snp	A/G	0.000399281	0.0141238	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91455414	ACCCACTTGTTGATG[A/G]GGTTGTTTGTTTTTT	143279
rs185059673	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HECTD2, HECTD2-AS1	GRCh38.p7	10:91514985	TATTTGAAAGATCAC[A/G]CAGCTATTCCACCAA	143279
rs185061189	snp	C/G	0.00478085	0.0486577	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409883	CTTGCCCGCGGGACT[C/G]GGCGCCGCAGGCCAG	143279

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