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

DTX2

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs544065076	snp	C/T	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76490288	CCAAGATCACACCAC[C/T]GCACTCCAGCCTGGT	113878
rs544130333	snp	A/G	0.00874735	0.0655527	utr-variant-5-prime, upstream-variant-2KB	DTX2	GRCh38.p7	7:76480450	CTGGGCAATGACCCC[A/G]GGACTCCAGGCCAGA	113878
rs544147973	snp	A/G			intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501787	CTGTCCGTCCTCCCC[A/G]TTTGGTGGCTTCTGC	113878
rs544213095	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76472781	AAAAGGTCTTCTATC[A/G]TTTCTCCACTCAAAG	113878
rs544329534	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76500058	CGTGGTGCCACAACG[C/T]CCCCTGGAGTAGTTT	113878
rs544329584	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76504961	GGAGCTTTGGAAAAG[C/T]TCTGGCCGTGTGAGA	113878
rs544336070	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	DTX2	GRCh38.p7	7:76463526	TAAAACCTGATCATC[A/T]TCTTCCTCGTTGGCA	113878
rs544421823	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76488913	AAAAAAAAAAAGTGG[A/G]GGGAAGAGTTGAAAC	113878
rs544471494	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502238	CCTCTTTTTCCAAGA[C/T]TGGCCCACGTCAGCC	113878
rs544471592	snp	A/C	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76491837	CACCACCACACTTGG[A/C]AGACTTTTAAAAATT	113878
rs544508356	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501781	CCTGCCCTGTCCGTC[A/C]TCCCCATTTGGTGGC	113878
rs544517113	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505960	GCTTCTTTTACCTCA[A/G]TTTTGTTTGCAATAA	113878
rs544786090	snp	G/T	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76501052	TCAGACTCCTGTTGC[G/T]CTTCCATAGAACCTG	113878
rs545079051	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, intron-variant	DTX2	GRCh38.p7	7:76463689	AAGGGACAGTTTGTG[C/T]CAGCTCTCCAGAGAG	113878
rs545096122	snp	A/G	0.00119737	0.0244387	intron-variant	DTX2	GRCh38.p7	7:76490408	CTTGATTTTTCACCA[A/G]TTTCCCACTACTGTC	113878
rs545218718	snp	A/G	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76481119	ACTCAGTGGCTGTGT[A/G]CCCTGGGCAGGCAAC	113878
rs545245337	snp	A/C			intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474075	TACAGGCATGTGCCA[A/C]CACGCCCGGCAAATT	113878
rs545266927	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76494885	CTGGAGAGCAGTGTC[C/T]TGTCACCCTGGTGTG	113878
rs545303902	snp	C/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76493331	CCCCTGGGCTGAAGC[C/G]ATCCTTCTGCCTCAG	113878
rs545321713	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502276	CTGTTGGCGAGCATG[A/C]CCCATGTTTGGTCTC	113878
rs545347146	snp	C/T	6.97618e-05	0.00590559	missense	DTX2	GRCh38.p7	7:76505441	GCACGTCCAGCACCA[C/T]GGGTGAGACGGACAC	113878
rs545465455	snp	C/G	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501826	CGGGCCTGTGCTGCT[C/G]GTAAGCCCTTCAGAG	113878
rs545565669	snp	C/T	0.000133905	0.00818134	missense, intron-variant	DTX2	GRCh38.p7	7:76503534	ATGTCGCTCCCCGGC[C/T]ACGAGGACTGCGGGA	113878
rs545618548	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76496273	AGTGGCTGGCCTGGC[C/T]GCCCTTCACCCCTGA	113878
rs545664021	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76483963	TTGGGAGACTGAGGC[A/G]GGAGGATTGCTGGAG	113878
rs545700963	snp	A/G	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76498208	TCAGCAGGTCCTCTC[A/G]GAGCCTCCGCTTAGC	113878
rs545759254	snp	C/T	0.00636936	0.0560724	intron-variant	DTX2	GRCh38.p7	7:76488862	GAGATCACGCCACTG[C/T]GCTCCAGCCTGGATG	113878
rs545800214	snp	A/C	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76468658	AGACAAGGTTTCACC[A/C]TGTTGGCCAGGCTGG	113878
rs545822100	snp	A/G	0.00517822	0.0506191	intron-variant	DTX2	GRCh38.p7	7:76486516	GCCCCCTGGGAACAG[A/G]CCGTGATACAAGAAA	113878
rs545910807	snp	G/T	0.0154538	0.0865337	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76478514	AACTCCTGGGCTCAA[G/T]CCATCCTCCTGCCTC	113878
rs546026257	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76503907	TGGGAGGAACCCTGC[A/G]GAGGGGCTGGAGAAG	113878
rs546097609	snp	A/C	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471572	CTCGCTCTGTTGCCC[A/C]GGTTGGAGTGTAGTG	113878
rs546234521	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471153	TTCTGGTTTCCATTC[A/G]TTCTTTTTTTTTTTT	113878
rs546274019	snp	A/C	0.00119737	0.0244387	intron-variant	DTX2	GRCh38.p7	7:76483353	GTCCTGGCGGTCACC[A/C]CACGGGTTAGAATCT	113878
rs546319627	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76497223	GACCTGTGCGTCCCC[A/G]TGGCCATTGATGGTG	113878
rs546439085	snp	A/G	0.021333	0.101051	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76477602	CGTGCCTGTAGTCTC[A/G]GCTGGGTGACAGAGG	113878
rs546463318	snp	A/G	0.0023933	0.0345097	intron-variant	DTX2	GRCh38.p7	7:76505072	GGTGGGCGGGCGCTC[A/G]TCCAGCAACGGCTGT	113878
rs546589733	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76469253	CCAGAGAGGACGTTC[C/T]AGCCACCATTGCAGT	113878
rs546698253	snp	A/G	0.000111744	0.00747393	intron-variant	DTX2	GRCh38.p7	7:76497526	GCTAAGCCTCCTTCC[A/G]GCCTCGCTGCCTCTG	113878
rs546707018	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76504251	GGAAATTCAGGAACA[C/T]TCGGGGTTGGCATCT	113878
rs546980105	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76500749	AGCCCCTCCTCTCCC[A/G]GCCCTGGCCTCTCCA	113878
rs547118841	snp	A/G	0.00199481	0.0315187	intron-variant	DTX2	GRCh38.p7	7:76464239	CTTAGAAAGTGGGGC[A/G]CAGTCACCTGGGAGA	113878
rs547124539	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	DTX2	GRCh38.p7	7:76506168	CGGTACTGGGCTGTG[C/T]GGCCTCCACATGCCC	113878
rs547143607	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76480177	GGGTGTGGTGGTGAA[C/T]GCCTATTGTCCCAGC	113878
rs547211112	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76500249	GGTGGGACTGGGGAA[A/G]GCTTTGCCCGACGGA	113878
rs547274028	snp	C/T	0.00318978	0.0398085	intron-variant	DTX2	GRCh38.p7	7:76488149	GAGCTTTCTACAGAA[C/T]ATTCTCCTGGTTCCT	113878
rs547397112	snp	A/G	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76494608	GGTCCTGTCCAGGCT[A/G]TGTCCCAAATTGTCC	113878
rs547546799	snp	C/T	0.00358779	0.0422022	intron-variant	DTX2	GRCh38.p7	7:76466743	AGCTAGGATTACAGG[C/T]ATGCGCCACCATGCC	113878
rs547656205	snp	G/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76495378	TTCACTCTTCAGGGC[G/T]CTGACAGCGGGAATC	113878
rs547701065	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76481989	AGGCTCGAGCCGTCA[C/T]GCCCAGCCCTGGAAA	113878
rs547739980	in-del	-/T			intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474225	CTTTCTTTCTTTTCT[-/T]TTTTTTTTTTTAAGA	113878
rs547751606	snp	G/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76503246	TGGCATGAGTTGCTG[G/T]TGCAAAACAAAGCTT	113878
rs547856779	snp	G/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76502780	CCACTTGTAAGCACC[G/T]CAGACACTGTCTCCC	113878
rs547885065	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76476873	GCCTGGGCCATGGTG[C/T]GCCCTCCATTGGGGA	113878
rs547899687	snp	C/T	7.19645e-05	0.00599809	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502477	CCCACTGGCCCAGGG[C/T]GGAGGCGGGTGGCCC	113878
rs547921752	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76476186	TTGAGGCTTTTTCCC[A/G]TGGCCAATTATAATA	113878
rs548004885	snp	A/T	0.00119737	0.0244387	intron-variant	DTX2	GRCh38.p7	7:76467400	CTGAATATCTCCTCT[A/T]ATGTTTATTGGCATA	113878
rs548128521	snp	G/T	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76495466	GGCTGTCAGGAGTTT[G/T]GGGGGCTGTCCCTAG	113878
rs548465387	snp	C/G	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76496043	AGGAACCGCATTTGA[C/G]CCCAGGAACAAGCTT	113878
rs548469172	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76476403	GGTGCCTGTGCCCCT[C/G]GAGCAGAAGGCTCAC	113878
rs548585067	snp	C/T			intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502199	TGACTTTGACTGCAC[C/T]TCCAGCATTTCAGCA	113878
rs548593041	snp	C/T	0.0314385	0.121371	intron-variant	DTX2	GRCh38.p7	7:76467750	ATAATGGCACTGAGA[C/T]GTCATGTGGGCATTG	113878
rs548629834	snp	A/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76476921	GAAAGTTTTAGCTGA[A/T]GTCCTCGCCTGTATT	113878
rs548876627	snp	C/T	0.00517822	0.0506191	intron-variant	DTX2	GRCh38.p7	7:76504040	GGAGACTCAGACGGG[C/T]CCTAGCCCTTTCGGT	113878
rs548880756	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76497565	GCACAGACCCTCTTC[C/T]TTCTCTCTGCTCCCT	113878
rs548913215	snp	C/T	0.000235612	0.0108513	intron-variant	DTX2	GRCh38.p7	7:76503626	CACTCCTGGCCACTC[C/T]TCTTCCCACCCCGCC	113878
rs548945034	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	DTX2	GRCh38.p7	7:76460995	GCCACCACGCCCGGC[C/T]AGTTTTTTTTGGTAT	113878
rs548988496	snp	A/G	0.00159617	0.0282053	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76472170	TGGGGGGATGTGTCT[A/G]CTGTCAGGGAGGTGC	113878
rs549025603	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76480288	GTAGCCTGGGTGAGA[A/G]AGTGAGACCCTGTAA	113878
rs549074404	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76472996	AATTGTTTTCTTTTC[C/T]GTTTTTTTTAATAAA	113878
rs549150805	snp	A/T			intron-variant	DTX2	GRCh38.p7	7:76463155	TGGTGACTCGAGCCT[A/T]TAATCCCAGCTACTC	113878
rs549150958	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76464298	TACCGGGACACAGCT[A/G]GGCTACTGTAAGTAG	113878
rs549173941	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76481407	GGCCAGGCTGGTGTC[A/G]AGCTCCTGACCTCAG	113878
rs549193433	snp	C/G	0.0023933	0.0345097	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474506	CTTTCATCTTCTCTC[C/G]GGACGGCAGAGGCAG	113878
rs549210409	snp	A/G	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76492082	CCACTTGGCCATGAC[A/G]CAGTGTTTCTCCAGC	113878
rs549274842	snp	A/G	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501522	CTGGAACCGCCAGCA[A/G]GACCCCCAACTCACA	113878
rs549278980	snp	A/G	0.0023933	0.0345097	downstream-variant-500B	DTX2	GRCh38.p7	7:76506031	TGCATGCGTGTGTGC[A/G]CACTTGTGTGTGTGT	113878
rs549315930	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505764	CCTGCCTCTCTCTCC[C/T]CCTCCCCTCTGGGAA	113878
rs549378573	in-del	-/ACTG	0.00478085	0.0486577	intron-variant	DTX2	GRCh38.p7	7:76490898	CGTGGGGTTTATGAT[-/ACTG]ACCTGTCTTTTACTG	113878
rs549437537	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501850	TTCAGAGGCACAGGT[C/G]CCGGTGACTCACCTG	113878
rs549579003	snp	G/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76481950	TGATCCTCCTGCCTT[G/T]GCCTCCGAAAGTGTT	113878
rs549742474	snp	C/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474278	CAGACTGGTCTCAAA[C/T]GCCTGGCCTCAAGTG	113878
rs549785903	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	DTX2	GRCh38.p7	7:76461955	CGTGGGTGTGAGGGG[A/G]ACCGACGGCCGGGGC	113878
rs549873607	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76464100	GTTGTCAGTGTGATA[C/T]ATACTGAGCTGGGAG	113878
rs549943990	snp	A/G	0.00119737	0.0244387	intron-variant	DTX2	GRCh38.p7	7:76466702	GTTCAAGCTACTCCC[A/G]ATTCTCCTGCCTCAG	113878
rs549975041	snp	A/T	0.00636936	0.0560724	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76475097	AGATCACCTGAGGTC[A/T]GGAGTTCGAGACCAG	113878
rs550004840	snp	G/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76465117	CTGATTTAGAGGGTG[G/T]TTGCTTTCTGCTGGG	113878
rs550011717	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76481961	CCTTGGCCTCCGAAA[A/G]TGTTGGGATTACAGG	113878
rs550083900	snp	A/G	5.04401e-05	0.0050217	missense, downstream-variant-500B	DTX2	GRCh38.p7	7:76502370	GACAGCAAGGCAATC[A/G]GGTCCCTAGCTGTGG	113878
rs550117954	snp	C/T			missense	DTX2	GRCh38.p7	7:76482919	CTGCATACCCCGTCC[C/T]CCAGCACCCCCCACA	113878
rs550120252	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76501921	TGAGACGGAGTCTCG[C/G]TCTGTCACCCAGGCT	113878
rs550244776	snp	C/G	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76494371	GAAATCACAGTGTAC[C/G]GTGTGTGCATGTGCG	113878
rs550348866	snp	A/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76483425	GCAGAGTTAAAGGCC[A/T]GTGGCCTCTGCTTGC	113878
rs550352074	snp	C/T	0.00119737	0.0244387	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471310	GGGACTACAGGCACC[C/T]GCCACCGCGCCCGGC	113878
rs550380032	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76475692	CTCCTTCTCAAAAAT[A/T]AAAAAAAAGAAAAAA	113878
rs550389043	snp	A/G	0.00199481	0.0315187	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76470075	GAGCCTTCTCTCCCC[A/G]CCCTTGCAGTCTCTA	113878
rs550530960	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76479716	AACCTACCCGGGAGG[C/T]GGAGGTTGCAGTGAG	113878
rs550617052	snp	C/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76478662	AAACCACCCTCCTGT[C/G]GCAGCCTCCCTAAAC	113878
rs550638982	snp	A/G	0.0836354	0.186609	intron-variant	DTX2	GRCh38.p7	7:76500793	ATCCTGGGAGCAGGA[A/G]TTCCAGAGACAAGGG	113878
rs550675743	snp	C/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76500335	GTCTGGGCCCCTCTC[C/G]CATTTCCTCCTGGCA	113878
rs550795048	in-del	-/C	0.00517822	0.0506191	intron-variant	DTX2	GRCh38.p7	7:76486417	AAGCCCGAGAACCGA[-/C]TTTTTACTGGCAGCC	113878
rs550804327	snp	C/G	0.000167631	0.00915353	intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501326	AGGAGCCTGAACGTC[C/G]TCCTCATGTGTCCCA	113878
rs550811814	snp	C/G	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76505193	GGTTCATGTGGGATC[C/G]TAATGTACTATCCAG	113878
rs550865746	snp	A/G	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76490884	CCAGAGCATCCTATC[A/G]TGGGGTTTATGATAC	113878
rs550961162	snp	A/G/T	8.74721e-05	0.00661281	synonymous-codon	DTX2	GRCh38.p7	7:76480722	CCAGGCAGACCCCTC[A/G/T]CTGGCCCCTTACATT	113878
rs551025065	snp	C/T			intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76472087	AAAGCCCCATCTCGC[C/T]GTGCTCACAGGACTA	113878
rs551262168	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76480342	GTGGAAAAGCATCAC[A/G]TGTTTCCCCTGCGCT	113878
rs551318957	snp	G/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471873	CTGGTTGACCACAAG[G/T]GAATTGTAGGTTACT	113878
rs551427698	snp	C/T	0.0252325	0.109451	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471396	TCGATCTCCTGACCT[C/T]GTGATCCGCCCGCCT	113878
rs551443469	snp	G/T	0.00711172	0.0592054	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505717	TGTTGAGGGTGTGGG[G/T]TGTGCCCCACCTGAA	113878
rs551446793	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76491142	AGCTGGGATTACAGG[C/T]GCCTGCCACCACGCC	113878
rs551465314	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76479815	AAACACACTAAGCAG[C/T]TGGGTCAGAGGGGAA	113878
rs551557928	in-del	-/G	0.0023933	0.0345097	intron-variant	DTX2	GRCh38.p7	7:76463932	TAAGACATGCTTTAT[-/G]GGGATAGAAGACACA	113878
rs551603171	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76492028	GCCTCCACACAGGCA[C/T]CCAAGGAGCGTAAAA	113878
rs551607052	snp	G/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76480852	CTGCGCCAGGTGTTG[G/T]GGTGATGGACGTGAC	113878
rs551608200	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501443	GTTTCACCCCAGGCT[C/T]CTCCTCTCCAAGCTG	113878
rs551648374	snp	G/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76505273	GAGTCACCTGGGAGG[G/T]GCTGGGATGGGAAGA	113878
rs551683893	in-del	-/CT	0.0217236	0.101931	intron-variant	DTX2	GRCh38.p7	7:76491716	TGAGACAGGGTCTCA[-/CT]CTGTCGCCCAGGCTG	113878
rs551713421	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76500916	GGAGAGCTGGTCAAG[A/G]TTCTTATAATTTTTT	113878
rs551848891	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76502949	GCCTACACATGAAGA[A/G]CCGCGCCCAGACTGA	113878
rs551998589	snp	A/G	5.54145e-05	0.00526347	missense, intron-variant	DTX2	GRCh38.p7	7:76497471	TTGAGGAAAATGTCC[A/G]TGAAAGGTAGTTCTT	113878
rs552000434	snp	A/G	3.30028e-05	0.00406205	missense	DTX2	GRCh38.p7	7:76482955	CCGCTTCTGTGTTTG[A/G]GACCCACCAGGCCTT	113878
rs552061290	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76473626	CCCTGGCCAACATAG[C/T]GAAACCCCGTTTCTA	113878
rs552061839	snp	A/C	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76483258	CCTAGGTGGTCCTGC[A/C]GTGGCATCTCATTTG	113878
rs552272442	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76503206	CTCGCCACCTGTCTC[C/T]TGATAGCATGTCCCT	113878
rs552283460	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	DTX2, FDPSP2	GRCh38.p7	7:76469783	GGCCAGTTTGTCCGT[C/T]GTCAGTCTGTCTTGG	113878
rs552396260	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76499350	AGAATTAAACAAACC[A/G]TGCCGACTCCAGCCT	113878
rs552573699	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76469217	GCCCTAGCCATAGGG[A/G]GTCATGGTAGCTGTG	113878
rs552576670	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76500122	GCCTCAGAAGCGCCG[A/G]GGTCGGTTCCTCACT	113878
rs552606802	snp	A/T			intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502121	CAAATTCCTGACCTC[A/T]AGTGATCGGCCTCCT	113878
rs552614190	snp	A/G	0.0158469	0.0875917	intron-variant, upstream-variant-2KB, utr-variant-5-prime	DTX2	GRCh38.p7	7:76477041	CGGCCGTGGCTGCCC[A/G]AGAGATGCGTGACAC	113878
rs552618975	snp	C/T	0.00676609	0.0577691	intron-variant	DTX2	GRCh38.p7	7:76504629	GACCTCACATAGCCT[C/T]GAGGGAGGAGGAGAG	113878
rs552652846	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76476687	TTGGGGGCTGGTATA[A/G]AGGGAGGATCAATTG	113878
rs552701459	snp	C/T	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76504080	TGAGCCAAGGTGGAT[C/T]GTAGGGCCTGGGGCA	113878
rs552755970	snp	C/T	0.00438332	0.0466095	intron-variant	DTX2	GRCh38.p7	7:76467097	GCAGAGGCAGCTTCA[C/T]TGTGTTGCCCAGGCT	113878
rs552800881	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76500892	GGCTGTCCTGCCCCC[C/T]GGCTATTGGGAGAGC	113878
rs552887109	snp	A/G	0.00159617	0.0282053	intron-variant	DTX2	GRCh38.p7	7:76484523	AGAGTGGTAGCTGGG[A/G]CAGGGCTTTCTGAGA	113878
rs552904573	snp	C/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76503762	GAGGCAGTGCCGGGG[C/G]TTAGGGTAAGCTCTT	113878
rs552923848	snp	G/T	0.00755907	0.0610114	intron-variant	DTX2	GRCh38.p7	7:76499277	TATTCGTCTTTCCCG[G/T]TTGAGATCAGGGAAC	113878
rs553157530	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76467991	CGGGCAGGGCATCCC[A/G]AGGACAGCTTTGGGT	113878
rs553328255	snp	C/T	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76484642	CTGGTCGGCATCCTG[C/T]TGCCTCCCTGCTCAC	113878
rs553406982	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76483601	CGGTGTGAGGGAGGG[C/T]AGAATGTGGAGCACG	113878
rs553443250	snp	C/G/T	0.000399281	0.0141238	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505876	GCTGCTTCGGGCCCG[C/G/T]GGTGCTCGGGGCCTG	113878
rs553445766	snp	C/T	0.0829062	0.185956	intron-variant	DTX2	GRCh38.p7	7:76497837	GTGTCTCGGGAAAGG[C/T]CCCCAGACAGCGGCC	113878
rs553600677	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501689	TCCTCCCTCTTCCGG[A/G]TGCCCACTCTGTGCT	113878
rs553643841	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76478219	TAGTTACAGTGACGT[C/T]CTCATAGTCGCATGG	113878
rs553666596	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76470579	GACAACAGATTTGTG[C/T]CTTTTTTCGGTGCAT	113878
rs553769368	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474597	AGTGATCAGATGGGT[C/T]TCTCACATATTGTTA	113878
rs553829288	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502087	AGATGGGGTTTTCCC[G/T]TGTTGGCCAGGCTGG	113878
rs553892445	snp	A/G	0.000399281	0.0141238	missense	DTX2	GRCh38.p7	7:76492199	CCAGGGAGCGTCCCT[A/G]CCACTGTGCCCATGC	113878
rs553904874	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76464528	GCCTCAAATTCCTGG[A/G]CTCTGGGGTAGCTGA	113878
rs554098349	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B, utr-variant-3-prime	DTX2	GRCh38.p7	7:76502222	TTTCAGCACATGAAA[A/G]CCTCTTTTTCCAAGA	113878
rs554132136	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76481621	AATGTTTGGAGACAT[C/T]GTTGGTTGTTACAGC	113878
rs554183579	snp	G/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76494917	TTGTGGGTTGAGGAA[G/T]TATACCATGCCCGGC	113878
rs554247902	snp	C/G			intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76479430	AGACATGAGGAGCTA[C/G]AACCTGTGCTGCAGT	113878
rs554346964	snp	C/G	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76481747	TAAGGAATTATTGGC[C/G]CACAGTGTCACCAGT	113878
rs554385895	snp	A/G	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76492361	CCTCAGGGAGAGCCA[A/G]AGGGGCTCCCTGGGG	113878
rs554423518	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76495755	CATAGAAACAGAGGG[A/G]AGTGCAAAGCAGGAG	113878
rs554628363	snp	A/G	0.00119737	0.0244387	intron-variant	DTX2	GRCh38.p7	7:76494745	CCTAAGGAAATAGGA[A/G]AGCCTGGAGGCTGTG	113878
rs554789796	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76482037	TGTCGTAGAGTCTGT[A/G]AAAACTGTGGCTGTC	113878
rs554845846	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474633	AAAGTAGCCGTGGCT[C/T]AGTATGAGTTGAGTA	113878
rs554863961	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76465436	GAATTTCATTCTAGA[A/G]ATCCAGGGGAGGTGT	113878
rs554940290	snp	C/G			intron-variant	DTX2	GRCh38.p7	7:76502759	AGGGCACCGCCTCCC[C/G]CTCGGCCACTTGTAA	113878
rs555030423	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76466945	CCTTGTAACCCAGGC[A/G]GCTGGAGTGCAGTGG	113878
rs555055291	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76504743	TAGACCAGGTGACCA[C/T]GGAAGGCTGGAGCAG	113878
rs555222086	snp	A/G	1.66358e-05	0.00288402	missense	DTX2	GRCh38.p7	7:76483024	CTGCGCCCAGGCTGA[A/G]CACCACCAACGCCTG	113878
rs555314149	snp	C/T	0.00159617	0.0282053	intron-variant	DTX2	GRCh38.p7	7:76495081	TGGCATAGCCCAGTC[C/T]CTCTATCGGGTGGGG	113878
rs555318591	snp	A/G	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76497260	CCTTGGCCTGAGCAG[A/G]GTTTGTTGGCGTCAC	113878
rs555380925	snp	A/G	0.00119737	0.0244387	utr-variant-5-prime, upstream-variant-2KB	DTX2	GRCh38.p7	7:76480428	GTTCACAGATCTGCC[A/G]GAGGCGCTGGGCAAT	113878
rs555386605	snp	C/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76500960	GGGTGCACACTGTCG[C/G]CCAGGCTCAGTGCAG	113878
rs555405513	snp	G/T	0.00318978	0.0398085	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76473974	TTGCCCAGGCTGGAG[G/T]GCAATGGCGCGATCT	113878
rs555428734	snp	A/G	0.00159617	0.0282053	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471451	CAGGTGTGAGCCACC[A/G]CGCCCAGCCTGGTTT	113878
rs555431510	in-del	-/T	0.354045	0.227321	intron-variant	DTX2	GRCh38.p7	7:76466594	TGTTTCTCTGTCTCT[-/T]TTTTTTTTTTCTTTG	113878
rs555442385	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76480996	CCCTTCCCCTTGTCT[C/T]GCAAAGCAGAAATGC	113878
rs555444007	snp	A/G	0.0023933	0.0345097	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76472602	AAAGTGCTGGGGATT[A/G]CAGGCATGAGCCACT	113878
rs555493452	snp	C/T	0.0319915	0.122361	intron-variant	DTX2	GRCh38.p7	7:76500546	TGGGACCTTGGCTGC[C/T]TTTGTTTCTGTTTGG	113878
rs555631457	snp	C/T	0.00557542	0.0525036	intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501741	CTCCCTTGTAAGACC[C/T]CACGCCGAGGGCCTC	113878
rs555652435	snp	A/G	0.0023933	0.0345097	intron-variant	DTX2	GRCh38.p7	7:76488662	GCACTTTGGGAGGCC[A/G]AGGTGGGTGGATCAC	113878
rs555731512	snp	A/C	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76463425	CCAGGCTATTGGAAA[A/C]TAAATCTGGTGATTT	113878
rs556099717	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76504969	GGAAAAGCTCTGGCC[A/G]TGTGAGAATGGGCTT	113878
rs556128089	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76481352	CCACCACACCTGGCT[A/G]ATTTTTGTATTTTTA	113878
rs556195156	snp	C/T	0.0134861	0.0810011	intron-variant	DTX2	GRCh38.p7	7:76464362	GCAGAGGGCTCTGAG[C/T]GAGGAGGGTTATGTG	113878
rs556256715	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	DTX2	GRCh38.p7	7:76463535	ATCATCTTCTTCCTC[A/G]TTGGCAAAGGTGCCT	113878
rs556327807	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474141	GGTCAGGCTGGTCTC[A/G]AACTCCCGACCTCAG	113878
rs556353071	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501532	CAGCAGGACCCCCAA[A/C]TCACACACAGCCCCA	113878
rs556438131	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76492426	AGAGTGAGCCCAGGT[A/G]CCCCTCCTTTTGCTC	113878
rs556443491	snp	G/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	DTX2	GRCh38.p7	7:76480452	GGGCAATGACCCCGG[G/T]ACTCCAGGCCAGAGG	113878
rs556476889	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502244	TTTCCAAGACTGGCC[C/G]ACGTCAGCCCAGCCC	113878
rs556566197	snp	G/T	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76481537	GGCACCAGTTTCCTC[G/T]CGGAGCCATCCCTTA	113878
rs556606345	snp	A/G	0.0023933	0.0345097	intron-variant	DTX2	GRCh38.p7	7:76469432	GATTCTCATTCTGTC[A/G]CCCAAGCTGGAGTGC	113878
rs556684382	in-del	-/A	0.0130921	0.0798413	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76475151	GTCTCTACTAAATAC[-/A]AAAAAAAAAATTAGC	113878
rs556815744	snp	C/G	5.85006e-05	0.00540804	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502498	CGGGTGGCCCGCCCC[C/G]ACAGTCCTGAGCTGT	113878
rs556833389	snp	A/G	0.00119737	0.0244387	intron-variant	DTX2	GRCh38.p7	7:76498135	CGCTCTTGAGTGGGC[A/G]TGGTGGCGGGCAGGG	113878
rs556835481	snp	C/T	0.00768562	0.0615121	intron-variant	DTX2	GRCh38.p7	7:76504492	GGGGCCCTGACCAGG[C/T]GGCAGGAGGCCAGGC	113878
rs556872387	snp	A/G	0.0329836	0.124112	intron-variant	DTX2	GRCh38.p7	7:76503818	CCTCCACTCTTTCCT[A/G]AACCAAGGAAGCCTT	113878
rs556896762	snp	C/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76499527	CCCCTTCTGGTCCTG[C/G]AGTCTGGGACGACCG	113878
rs556960778	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-5-prime, upstream-variant-2KB	DTX2	GRCh38.p7	7:76477165	GCCCGCCCGCCCGCC[C/T]GAGGGCACTCCAGGT	113878
rs557153724	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76488253	CAAGGACTTCTTGTT[C/T]GTTCTTTAGGAACGG	113878
rs557409474	snp	A/G	0.0337553	0.125452	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76479316	AGCAGGGGCCAGGTC[A/G]GGGAGTGGGTGCAGA	113878
rs557448393	snp	G/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76484997	AGACCCCAAGAGTGG[G/T]CTATCTGGGGCACAT	113878
rs557513342	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76478957	TTCACTCTGTCATTC[C/T]GAAGCAGTGTGTAGA	113878
rs557614022	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76496014	CTTCTCTCCACCCGA[C/T]ATTCAGTTCCCACAG	113878
rs557632160	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471048	GCATCTCCTGTCTCT[A/G]GGTGCCCCATCTCAT	113878
rs557690146	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76488508	TCCAACTACGGGCTT[A/G]AGCTCAGTGCTGCCC	113878
rs557693594	snp	A/T	0.00279162	0.0372561	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471534	GCTTGGCTGTTATTT[A/T]TTTTTTTTTAAAGAG	113878
rs557766488	snp	C/T	0.000414955	0.0143981	intron-variant	DTX2	GRCh38.p7	7:76500414	CTGTGCTCCTCAGGA[C/T]GCTGCTTATGTACTT	113878
rs557780702	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	DTX2, FDPSP2	GRCh38.p7	7:76469548	CAGGCGCTCGCCACC[A/G]CACTTGGCTAATTTT	113878
rs557905763	snp	G/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76504523	GCCACACTGGACTCT[G/T]CTTCTGCAGCGGAGG	113878
rs558087274	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76494815	ACCTACTGGGGGAGC[A/G]TTGTCTAGGGGAGCA	113878
rs558116272	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76472452	CTGCCTCAGCTTCCC[A/G]GGTAGCTGGGATTAC	113878
rs558206125	in-del	-/CTCA			intron-variant	DTX2	GRCh38.p7	7:76500132	CGCCGGGGTCGGTTC[-/CTCA]CTCAATGTGCGCGGG	113878
rs558211857	snp	C/T	1.66532e-05	0.00288554	missense	DTX2	GRCh38.p7	7:76482705	AACTACACTGTCAAC[C/T]ACACCACCCACACGC	113878
rs558217094	snp	G/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471740	TGCTGCCCCTATTAC[G/T]CCCCTACTTTGCCCT	113878
rs558250624	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76495642	CAGCAAACACAGAGG[A/G]CTGCAGGCTTCCCAG	113878
rs558383004	snp	A/G	0.00119737	0.0244387	intron-variant	DTX2	GRCh38.p7	7:76463309	TAAAAAATTTTAAAA[A/G]GAGCTCAGGGTTTTT	113878
rs558417941	snp	C/T	2.80792e-05	0.00374684	synonymous-codon	DTX2	GRCh38.p7	7:76505553	GCAGAACGTGCTGGC[C/T]GAGCTGGCTGCCCAG	113878
rs558518627	snp	C/T	0.0130921	0.0798413	intron-variant	DTX2	GRCh38.p7	7:76505102	TGGAAGCAGGGAGGA[C/T]TCGAGCATGGTGCCT	113878
rs558543165	snp	G/T	0.00199481	0.0315187	intron-variant	DTX2	GRCh38.p7	7:76467889	CGATGGGCATTCTCA[G/T]TGGGGGACGAAGGGC	113878
rs558710880	snp	C/T	0.00199481	0.0315187	intron-variant	DTX2	GRCh38.p7	7:76483584	GCAAGGGGCTGTCAG[C/T]GCGGTGTGAGGGAGG	113878
rs558763490	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76476514	TGTTTTGGTGGGGAG[A/G]AGGCCACTGAAACCA	113878
rs558816292	snp	C/T	0.00676609	0.0577691	intron-variant	DTX2	GRCh38.p7	7:76465769	TATTTTTAGTAGAGA[C/T]GGGGTTTCCCTCTGT	113878
rs558902478	snp	C/G			intron-variant	DTX2	GRCh38.p7	7:76494277	GAGAGGAGCTGGAGT[C/G]GGGCAGGGGAGACAG	113878
rs558962720	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76475292	CTCCAGCCTGGGCAA[C/G]AAGAATGAAACTCTG	113878
rs559041165	in-del	-/T	0.158962	0.232835	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76478415	CTGCATCAGCTCTGA[-/T]TTTTTTTTTTTTTTT	113878
rs559041708	snp	C/T	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76503374	CGGTGGAGGTGACGG[C/T]CTTGGGTGTTCTCAG	113878
rs559093030	snp	A/G	6.5987e-05	0.00574362	missense, intron-variant	DTX2	GRCh38.p7	7:76497339	CACACCCGTGCAGGC[A/G]TGACGAGTGTTCTGA	113878
rs559121206	snp	C/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76464892	ACTGAAAAGGAACTT[C/G]CTAAGAGGGTGTTTT	113878
rs559156206	snp	A/G	0.0115144	0.0749975	intron-variant	DTX2	GRCh38.p7	7:76497707	CCAGTCACAGCTGGC[A/G]TGAGGGGGCTTGTTC	113878
rs559156215	snp	A/G/T	6.70493e-05	0.00578971	missense	DTX2	GRCh38.p7	7:76483044	ACCAACGCCTGGGGC[A/G/T]CAGCTCCTCCTTCCC	113878
rs559188806	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76477939	GAACAAACCCAGGTC[A/G]GGTCTGGCTCTAAGG	113878
rs559297188	snp	C/G	0.00199481	0.0315187	intron-variant	DTX2	GRCh38.p7	7:76496373	AGCCGGCTGTGCCCA[C/G]CTCCTGAGCCAGGTT	113878
rs559316443	snp	C/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76483564	CCCCTGAGCCCTAGT[C/G]TAGTGCAAGGGGCTG	113878
rs559439445	snp	C/T	9.90982e-05	0.00703841	missense, intron-variant	DTX2	GRCh38.p7	7:76497361	GTGTTCTGATGTCAG[C/T]CATTGGACTCCCTGT	113878
rs559605865	snp	A/G	3.55682e-05	0.00421697	intron-variant	DTX2	GRCh38.p7	7:76483153	GTGCAGTCAGGTATC[A/G]TGGGCAACGGCCGCT	113878
rs559640949	in-del	-/T	0.29432	0.24604	upstream-variant-2KB	DTX2	GRCh38.p7	7:76460830	TTCTTCTTCTTCGTC[-/T]TTTTTTTTTTTTTCT	113878
rs559738855	snp	C/T	1.64849e-05	0.00287092	synonymous-codon	DTX2	GRCh38.p7	7:76482911	CAACCTCCCTGCATA[C/T]CCCGTCCCCCAGCAC	113878
rs559903456	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76476882	ATGGTGCGCCCTCCA[C/T]TGGGGAGGCTGCGTG	113878
rs559936836	snp	A/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76468997	CTCAAACTCCTGGCC[A/T]CAAATGATCCACCCA	113878
rs560047651	snp	C/T	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76501053	CAGACTCCTGTTGCG[C/T]TTCCATAGAACCTGA	113878
rs560091232	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	DTX2, FDPSP2	GRCh38.p7	7:76469670	AGTGCTGGGATTACA[A/G]GTGTGAGCCACTGAG	113878
rs560126879	snp	G/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76472965	ATTTTTAAACCTCTT[G/T]ATACATATATTACCA	113878
rs560212817	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB	DTX2	GRCh38.p7	7:76460967	TCCCGAGTAGCTGGG[A/G]TTACAGGCACGAGCC	113878
rs560302738	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76480240	AGACCAGGAGTTTGA[C/G]GCTGCTGTGAGCCAA	113878
rs560303017	snp	C/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76490616	GACAAAGATAATGCC[C/G]TTTATTATTTCTTTT	113878
rs560328680	snp	A/G	0.00199481	0.0315187	intron-variant	DTX2	GRCh38.p7	7:76503106	CCAGGGCCCAGCTCC[A/G]CAGATCAGACGCTGC	113878
rs560383485	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76463717	GAGAAAAGGTGAGAG[C/T]CATGGGGACTTGACC	113878
rs560388357	snp	A/C	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76482385	TAAATAAACAAATAG[A/C]AGCATGACTGTGTAC	113878
rs560390290	snp	C/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474942	GTGGCGAAGACCTGA[C/T]GAGAGACTGTAAAGG	113878
rs560407577	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501833	GTGCTGCTGGTAAGC[C/G]CTTCAGAGGCACAGG	113878
rs560428912	snp	C/T	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76481924	GCTGGTCTTCAACTC[C/T]TGAGCTCAAGTGATC	113878
rs560686132	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76493573	GGTATGTAAGGAGGT[A/G]GATGGCGCCATCGTT	113878
rs560894212	snp	A/T	0.499137	0.0207489	intron-variant	DTX2	GRCh38.p7	7:76491688	GTTTTCAGAGTCTTT[A/T]TTTTTTTTTTTTTGA	113878
rs560944828	snp	C/T	0.0448719	0.142907	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474181	GCCTGGCCTACTTTT[C/T]TTTTTCTTTTTCTTT	113878
rs560983562	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76473021	AATAAATAGAGATGG[A/G]GGTCTCTCTGTGTTG	113878
rs561057322	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76481175	CTGCTTTTTGGTCTG[C/T]GATGTGTTTTGATCT	113878
rs561061534	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76480221	GAGTTGTGAGGATTG[C/T]TTGAGACCAGGAGTT	113878
rs561098852	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76463984	AGTGGCAGTTTTCAT[C/T]TCTTTTGTTGCATAA	113878
rs561187469	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76464679	TAGGATTACAGGCCT[A/G]AGCCACCGTGCCTGG	113878
rs561215956	snp	C/T	0.0123036	0.0774623	downstream-variant-500B	DTX2	GRCh38.p7	7:76506048	ACTTGTGTGTGTGTG[C/T]GCCCCCCCCCACTTC	113878
rs561225811	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76476786	CGGGCTTGGTGTGAG[C/T]AGGAACAGTGGCTGG	113878
rs561238228	snp	C/T	1.67764e-05	0.00289619	synonymous-codon, downstream-variant-500B	DTX2	GRCh38.p7	7:76502354	ATACAGCGATGTGAC[C/T]GACAGCAAGGCAATC	113878
rs561240011	snp	A/G	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76466661	CAATGGCACGATCTC[A/G]GCTCACTGCAACCTC	113878
rs561259457	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76493895	GGGCTTGGCGTGTGT[A/G]AATTCATTTCGTCCT	113878
rs561266344	snp	C/G	0.00874735	0.0655527	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76475553	TTAGCCAGGCGTAGT[C/G]GTGCGTGCCTGTAAT	113878
rs561402758	snp	A/G	0.00318978	0.0398085	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502592	CTGGGCGTGGGGCCA[A/G]CTTGAAGACCTTTCT	113878
rs561490883	snp	C/G/T	0.000143465	0.0084684	intron-variant	DTX2	GRCh38.p7	7:76482489	AGCAGACTAACCTTT[C/G/T]GTTTTCCTTTGAAAA	113878
rs561620655	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76499999	ACCCCAGACTCCCTT[A/G]TCCCTGTGATGTTCA	113878
rs561627789	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76480080	TGGGAAGGCTGAGGC[A/G]AGTCTATCCCTTGAG	113878
rs561632311	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76503954	TGTGCGTCGAGGAAC[C/T]TTGGGTTGGGAGTGG	113878
rs561662161	snp	C/T	0.0134861	0.0810011	intron-variant	DTX2	GRCh38.p7	7:76497788	GCCCGGCTCAGGATG[C/T]GGGGACAACCGTCCC	113878
rs561664014	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76479616	GAAACCCCGTCTCTA[C/T]TAAAAATACAAAAAA	113878
rs561688364	snp	C/T	0.0854556	0.188216	intron-variant	DTX2	GRCh38.p7	7:76487757	CCTGCATAGAAAACT[C/T]GGAGTCCTCATGTCT	113878
rs561788141	snp	A/G	0.00119737	0.0244387	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471768	CCTCTGGGTAGGCCC[A/G]TAAACCAGGGCTCCA	113878
rs561792861	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76504540	TTCTGCAGCGGAGGA[C/T]AGAGGCTGAGGCCGG	113878
rs561849241	snp	A/C	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76498389	CACGCCCTGCCCTTC[A/C]CCTGCCCTGGGGGAG	113878
rs561918063	snp	C/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76500760	TCCCGGCCCTGGCCT[C/G]TCCATAGCCTGATGG	113878
rs562073705	snp	A/G	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76501180	CGGCCGGGAGTACCA[A/G]TACCCAGAGATCTTC	113878
rs562179171	snp	C/G	0.0600435	0.162532	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505612	AGTGACCTCGCACCC[C/G]AGCACGCCCGCCTCT	113878
rs562236432	snp	C/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76490748	AAGTAGCTGGGACCA[C/G]AGGTGCATGCCACCA	113878
rs562321812	snp	C/G	3.61037e-05	0.00424859	intron-variant	DTX2	GRCh38.p7	7:76482476	TCTTGGGGATGCTAG[C/G]AGACTAACCTTTTGT	113878
rs562437206	snp	A/G	0.0217236	0.101931	intron-variant	DTX2	GRCh38.p7	7:76500080	GAGTAGTTTGTGCCC[A/G]AAGCGGCTGTCTGAC	113878
rs562565130	snp	A/G	0.0189856	0.0955633	intron-variant	DTX2	GRCh38.p7	7:76489426	ATTGCCCTCCAGCCT[A/G]GGTAACAGAGCAAGA	113878
rs562598877	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76479727	GAGGTGGAGGTTGCA[G/T]TGAGCCGAGATCACA	113878
rs562604077	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76500662	AGCCCCTTTGGTTTC[A/G]TCTCCCAGCCTCCCG	113878
rs562604237	snp	C/T	0.00119737	0.0244387	intron-variant	DTX2	GRCh38.p7	7:76487947	GCCCCCATCTGGGAA[C/T]GTTCTGCAGGTCCGA	113878
rs562660665	snp	C/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471844	GAGCCAGTGGGTTCT[C/T]GGTTCTGGAGAAGCT	113878
rs562754098	snp	C/T	0.000167997	0.00916352	intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501329	AGCCTGAACGTCCTC[C/T]TCATGTGTCCCACCC	113878
rs562785135	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76472881	TGCTGTAGTGAATAG[C/T]TTCACGTCAAAATTT	113878
rs562879704	snp	A/C	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76491895	GCCCAGGCTGGTCTC[A/C]AACTCCTGGCCTCAA	113878
rs562988333	snp	C/T	0.0166325	0.0896639	intron-variant	DTX2	GRCh38.p7	7:76467145	CTCAAGCAATTCACC[C/T]GCCTTGGCCTCCCAA	113878
rs563038526	snp	C/T	0.00119737	0.0244387	intron-variant	DTX2	GRCh38.p7	7:76481229	TCTGGCTCTGTTGCC[C/T]AAACTGGAGTGCAGT	113878
rs563104288	snp	C/G	0.0023933	0.0345097	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505970	CCTCAATTTTGTTTG[C/G]AATAAATGCTCTATA	113878
rs563113707	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76496096	CCCGGGCTCAAACCT[C/T]TGTCCTCTGATGCAC	113878
rs563117666	snp	C/T	5.02433e-05	0.0050119	missense, intron-variant	DTX2	GRCh38.p7	7:76503510	AAGATGGAGGTATTA[C/T]GGTTCCAGATGTCGC	113878
rs563493514	snp	C/G	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76483838	GCAGGAAGATCATTT[C/G]AACCCAGCAGTCAGA	113878
rs563754213	snp	C/T	0.00953873	0.0683987	intron-variant, downstream-variant-500B	DTX2, FDPSP2	GRCh38.p7	7:76469763	CCAAGCAAAACACAT[C/T]TACAGGCCAGTTTGT	113878
rs563779219	in-del	-/GCGGCT	0.499265	0.0191552	intron-variant	DTX2	GRCh38.p7	7:76486846	TTTCTGTTGTGGTGG[-/GCGGCT]GCTGCTGCTGCTGCT	113878
rs563829530	snp	A/C	0.000331148	0.0128633	intron-variant	DTX2	GRCh38.p7	7:76497493	GTAGTTCTTGTTCCC[A/C]AAAGCTCTCTGGCCT	113878
rs564015216	snp	C/G	0.00119737	0.0244387	intron-variant	DTX2	GRCh38.p7	7:76504047	CAGACGGGCCCTAGC[C/G]CTTTCGGTCTCCTGT	113878
rs564039055	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76478527	AAGCCATCCTCCTGC[C/T]TCAGCCTCTTGAGTA	113878
rs564099764	snp	C/T	0.00318978	0.0398085	intron-variant	DTX2	GRCh38.p7	7:76498236	AGCAGAGGGGCTTGG[C/T]GAGGTCTAGGAAATA	113878
rs564134904	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76503913	GAACCCTGCGGAGGG[A/G]CTGGAGAAGCGGGGC	113878
rs564447466	snp	A/G	0.00676609	0.0577691	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471188	TTTTTTTGAGACGGA[A/G]TCTTGCTCTGTCGCC	113878
rs564467059	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	DTX2, FDPSP2	GRCh38.p7	7:76469825	GGAACTCTGGAAACA[C/G]ATTTGGGTTTTCTCA	113878
rs564613301	snp	C/G	0.00279162	0.0372561	intron-variant	DTX2	GRCh38.p7	7:76500688	TCCCGAGACCCACAT[C/G]GTTATGGTCTGAGCT	113878
rs564669495	snp	A/G	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76504630	ACCTCACATAGCCTC[A/G]AGGGAGGAGGAGAGG	113878
rs564975774	snp	A/G	0.00199481	0.0315187	intron-variant	DTX2	GRCh38.p7	7:76464173	TAGAGGGAAGGTCAG[A/G]AAGGCTCCTGGAAGG	113878
rs565013473	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474905	CATGGTGCCTCAGCC[A/G]CGATCCTCTGGACAG	113878
rs565163871	in-del	-/TG	0.00398564	0.0444627	intron-variant	DTX2	GRCh38.p7	7:76483606	TGAGGGAGGGCAGAA[-/TG]TGGAGCACGTGGCAG	113878
rs565252434	snp	A/G	0.00199481	0.0315187	intron-variant	DTX2	GRCh38.p7	7:76495086	TAGCCCAGTCCCTCT[A/G]TCGGGTGGGGGCAGG	113878
rs565313194	snp	C/T	0.00159617	0.0282053	downstream-variant-500B	DTX2	GRCh38.p7	7:76506206	ATCTCCCTGCCATGC[C/T]AGAGGCTGTCACCCC	113878
rs565377740	snp	A/G	0.000115533	0.00759957	missense	DTX2	GRCh38.p7	7:76482877	GCCCCGTGTCAGGCC[A/G]CTACCGCCACTCCAT	113878
rs565461048	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76477211	GGTTGTGGGCTTTTG[C/T]CGGAGGAATTGGCAG	113878
rs565594421	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76467306	CTCCACAGTCTTACC[A/G]ACATTTGCTGTTGGC	113878
rs565679856	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502129	TGACCTCAAGTGATC[A/G]GCCTCCTAGAGTGCT	113878
rs565766204	in-del	-/G	0.0103295	0.0711199	intron-variant	DTX2	GRCh38.p7	7:76492295	CAGTCTGTGCCCTGC[-/G]GGACTTGGTGGGGAG	113878
rs565835497	snp	A/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76494706	TTTACTTGTGGGGAA[A/T]TAGATTCGGGAAGCT	113878
rs565864215	snp	C/T	0.00716266	0.059414	intron-variant	DTX2	GRCh38.p7	7:76495386	TCAGGGCTCTGACAG[C/T]GGGAATCCTCCCAGA	113878
rs565898747	in-del	-/T	0.282105	0.24793	intron-variant	DTX2	GRCh38.p7	7:76491297	CACTGCACCCAGCCA[-/T]TTTTTTTTTTTTTTT	113878
rs565972136	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76475198	TGCCTGTAATCCCAG[C/G]TACTTGGAAGGCTGA	113878
rs565972500	snp	G/T	3.31274e-05	0.00406972	missense	DTX2	GRCh38.p7	7:76482644	CTATCTGGAGCAGCA[G/T]GTGGCCAGGGGCAAC	113878
rs566020104	snp	C/T	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76467523	ATTGCTGATTTTAAT[C/T]CTTCGTGTCTATTGC	113878
rs566363463	in-del	-/G	0.00159617	0.0282053	intron-variant	DTX2	GRCh38.p7	7:76468954	TTTTTTGGTAGATAC[-/G]GGGTTTCACTGTATT	113878
rs566416146	snp	A/T	0.000798403	0.0199641	intron-variant, utr-variant-5-prime, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76470302	AATTTTCCTTCAGGA[A/T]CTGGTACTGTTCTGG	113878
rs566428149	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76479828	AGTTGGGTCAGAGGG[A/G]AATTATCAGTAGCAA	113878
rs566458418	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471431	CTCCCAAAGTGCTGG[A/G]ATTACAGGTGTGAGC	113878
rs566539313	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76472149	CATTTTTGTGGAGCT[C/T]GGGGATGGGGGGATG	113878
rs566618410	snp	A/G	0.00279162	0.0372561	intron-variant	DTX2	GRCh38.p7	7:76480894	CTGCTCTCTCCCTGC[A/G]GCACACGTGGTGGTG	113878
rs566635576	snp	C/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76504770	GCAGTGGTGTCTGCA[C/G]TGAGACATGAATAGG	113878
rs566676772	snp	A/G	0.00119737	0.0244387	intron-variant	DTX2	GRCh38.p7	7:76481376	ATTTTTAGTAGAGAC[A/G]GGGTTTTGCCACGTT	113878
rs566691920	snp	A/G	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76505300	AAGAACATGGTGCCA[A/G]CCCGTGCCTGCTCAC	113878
rs566757410	snp	C/T	0.0023933	0.0345097	intron-variant	DTX2	GRCh38.p7	7:76500921	GCTGGTCAAGGTTCT[C/T]ATAATTTTTTTATTC	113878
rs566839780	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474330	AAAACGCTGAGATTA[C/T]AGGTGTGAGCCACCA	113878
rs566905168	snp	A/G	0.0119091	0.0762411	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76473826	GAAAAGAACTCACCT[A/G]TTTTGCAAAGGAGCT	113878
rs566984725	snp	A/G	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76491143	GCTGGGATTACAGGC[A/G]CCTGCCACCACGCCT	113878
rs567112085	snp	A/T			intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76476900	GGGAGGCTGCGTGCC[A/T]TCGTGGAAAGTTTTA	113878
rs567363470	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	DTX2	GRCh38.p7	7:76461243	AGAGAGAAAAAAAGA[A/C]AAGAAAAAGACAAAA	113878
rs567455041	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505765	CTGCCTCTCTCTCCT[C/T]CTCCCCTCTGGGAAT	113878
rs567477593	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76475055	CTCACGCCTGTAATC[C/T]CAGCACTTTGGAAGG	113878
rs567487442	snp	C/T	0.00874735	0.0655527	intron-variant	DTX2	GRCh38.p7	7:76464301	CGGGACACAGCTGGG[C/T]TACTGTAAGTAGCTT	113878
rs567492749	snp	C/T	0.0012312	0.0247807	intron-variant	DTX2	GRCh38.p7	7:76505357	CCTTCCTCTTCCCCC[C/T]CCTCCTCCCCGGGCA	113878
rs567558533	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76491190	TTTAGTAGAGACAGG[A/G]TTTTGCCATCTTGGC	113878
rs567622394	snp	A/G	0.00104907	0.0228787	intron-variant	DTX2	GRCh38.p7	7:76492102	GTTTCTCCAGCTCTC[A/G]TTTCCAATAAGTCAG	113878
rs567625337	snp	G/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76465049	GCTCAAGAGGTTCTT[G/T]TGCCTCAGCTTCCCG	113878
rs567671905	snp	C/T	0.00835141	0.0640778	intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501897	AATGGACTTTTTTTT[C/T]TTTTTTTCTGAGACG	113878
rs567779132	snp	C/T	0.00119737	0.0244387	intron-variant	DTX2	GRCh38.p7	7:76481436	AGGTGATCTGCCTGC[C/T]TCGGCCTCCCAAAGT	113878
rs567870042	snp	C/T	0.00119737	0.0244387	intron-variant	DTX2	GRCh38.p7	7:76469415	TTTTTTTTTTTGAGA[C/T]GGATTCTCATTCTGT	113878
rs567870185	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76478623	TCACTATGTTGCCCA[C/G]GCTGGCCTCAAACTC	113878
rs568051675	snp	C/T	0.00159617	0.0282053	intron-variant	DTX2	GRCh38.p7	7:76497227	TGTGCGTCCCCGTGG[C/T]CATTGATGGTGTCAC	113878
rs568066210	snp	G/T	7.04573e-05	0.00593495	intron-variant	DTX2	GRCh38.p7	7:76503614	TCTTGAGTCCCCCAC[G/T]CCTGGCCACTCCTCT	113878
rs568100026	snp	A/G	0.000399281	0.0141238	missense	DTX2	GRCh38.p7	7:76504408	CCAGAGGGTTTCCCC[A/G]CCAGTGCTACCTTCC	113878
rs568262109	snp	A/C/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76504712	GAGTGTGACAGGCAG[A/C/G]GACCGGGGGCTGTGT	113878
rs568568953	snp	G/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76500300	CGCTGAGCTCTCCCG[G/T]CCCGCACACTGGCCT	113878
rs568608765	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76470183	GATGAGACCCATAAC[A/G]TGGCTGTAACTGTCT	113878
rs568669610	snp	A/G	0.00119737	0.0244387	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471368	GGGTTTCACCATGTT[A/G]GCCACGATGGTCTCG	113878
rs568733861	snp	A/G	0.00119737	0.0244387	intron-variant	DTX2	GRCh38.p7	7:76484425	GTGAATGGGCTGGCC[A/G]TAGCCCTCTGACTGT	113878
rs568764472	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471506	AGGGCTGTGTTCCTG[A/G]ATGCGGGTTCCTGCT	113878
rs568764864	snp	G/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76489821	GAACGAGACTCTGTC[G/T]CAAAAAATCCAAAGA	113878
rs568807688	snp	C/T	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76477904	AAGGTCACACATACA[C/T]GACTAAGAGGCAGCA	113878
rs568882468	snp	C/T	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76498596	TGCTGTGCCCGGCCT[C/T]ACCAGGGCTGGGCAG	113878
rs569057717	snp	A/G	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76500840	CACTCTCCACCTTGC[A/G]GATGCTGGTGTAGAA	113878
rs569061275	snp	A/G			intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76470130	TTGTGCACAAGCCCC[A/G]GAAAGATGGCTGGGG	113878
rs569118562	snp	A/C	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76489906	AAAAAAAAAAACAAC[A/C]ACCTTTATTTTATGG	113878
rs569149424	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76463712	CCAGAGAGAAAAGGT[A/G]AGAGCCATGGGGACT	113878
rs569179504	snp	G/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76504724	CAGGGACCGGGGGCT[G/T]TGTTAGACCAGGTGA	113878
rs569218339	snp	G/T	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76505212	TGTACTATCCAGTGG[G/T]CAGTTTTGGGGTCCC	113878
rs569297323	snp	A/C	1.86232e-05	0.00305143	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502492	CGGAGGCGGGTGGCC[A/C]GCCCCCACAGTCCTG	113878
rs569326734	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76480354	CACGTGTTTCCCCTG[C/T]GCTGAGGCTGATTCT	113878
rs569522521	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76495568	CATTGAAAAGGACAC[A/G]TGTGTCACTCATGCG	113878
rs569531583	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76473264	CCCCCGTGGGTGGCC[A/G]TCTGCCCTGTGAGAA	113878
rs569772168	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76499693	AGAACGCCCCGGGCC[A/G]CGCCGATCCTCACCA	113878
rs569793695	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76491229	TCTTGAACTCCTGAC[C/T]TCGCGATCCACCCAC	113878
rs569847974	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76476927	TTTAGCTGATGTCCT[C/T]GCCTGTATTTCCCAG	113878
rs569884280	snp	G/T	6.59859e-05	0.00574357	missense	DTX2	GRCh38.p7	7:76482949	ACAGGACCGCTTCTG[G/T]GTTTGGGACCCACCA	113878
rs569962247	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76466962	CTGGAGTGCAGTGGC[A/G]TAATCACGGATCACT	113878
rs570024216	snp	G/T	0.0023933	0.0345097	intron-variant	DTX2	GRCh38.p7	7:76467860	GAATTAAGAGATGAG[G/T]AAGTGGACAAGTGCG	113878
rs570076992	in-del	-/T			intron-variant	DTX2	GRCh38.p7	7:76484904	GGCTGAGCAGTGTTC[-/T]TTCGCTTACAGGAGA	113878
rs570077712	snp	G/T	0.00159617	0.0282053	intron-variant	DTX2	GRCh38.p7	7:76495665	CTTCCCAGGGATCAG[G/T]CACTGCCCCAGCGGG	113878
rs570239747	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76496856	TACCCCAGCGCTGTC[A/G]CTGAAGGCCCTGGCA	113878
rs570283968	snp	A/G	0.00517822	0.0506191	intron-variant	DTX2	GRCh38.p7	7:76503360	CCTTTACCATCTGAC[A/G]GTGGAGGTGACGGTC	113878
rs570410506	snp	C/T	0.0107246	0.0724382	intron-variant	DTX2	GRCh38.p7	7:76497583	CTCTCTGCTCCCTGA[C/T]TCCTGGGGGAAGGGG	113878
rs570431895	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76502951	CTACACATGAAGAGC[C/T]GCGCCCAGACTGACC	113878
rs570576069	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-5-prime	DTX2, FDPSP2	GRCh38.p7	7:76476978	AGAGTTGGTTCATCC[A/G]GGCCATGAGGACATG	113878
rs570668870	snp	A/G	0.00597247	0.0543191	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76477574	GATGATACAATAGCC[A/G]GGCATGGTGGCGCGT	113878
rs570717880	in-del	-/TAAATAAA			intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76477801	GTGAGACTCGGACTC[-/TAAATAAA]TAAATAAATAAATAA	113878
rs570737881	snp	G/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76467902	CAGTGGGGGACGAAG[G/T]GCATGAAACATCCTG	113878
rs570962290	snp	A/G	0.00119737	0.0244387	intron-variant	DTX2	GRCh38.p7	7:76504081	GAGCCAAGGTGGATC[A/G]TAGGGCCTGGGGCAG	113878
rs570962646	snp	A/G	0.00119737	0.0244387	intron-variant	DTX2	GRCh38.p7	7:76503738	GAGCCATGGAGGGCC[A/G]GGAATGGGGAGGCAG	113878
rs571148023	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76488091	GCAGGGACACACACC[A/G]GGGAGGAACTGCGAT	113878
rs571149442	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76500155	ATGTGCGCGGGGATG[C/T]GGCTCCCAGGAGACT	113878
rs571150244	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76478974	AAGCAGTGTGTAGAA[C/G]ATTCTAGAACACTCA	113878
rs571187784	snp	A/G	0.00199481	0.0315187	intron-variant	DTX2	GRCh38.p7	7:76484551	AGAGTGCCCTGGTGC[A/G]GGTGGTGAGGGAGTG	113878
rs571385067	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502022	CTCCCGAGTAGCTGG[G/T]ATTATAGGCACCTGC	113878
rs571469160	snp	C/T	0.0134861	0.0810011	intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501581	CCAGACCCCCGAGGG[C/T]GCGCCTCTCCCTGAT	113878
rs571554992	snp	G/T	0.00119737	0.0244387	intron-variant	DTX2	GRCh38.p7	7:76481539	CACCAGTTTCCTCTC[G/T]GAGCCATCCCTTACT	113878
rs571593144	snp	C/T	0.00268597	0.0365482	synonymous-codon	DTX2	GRCh38.p7	7:76492180	CAGCGGTCCCTCAAG[C/T]AGCCCAGGGAGCGTC	113878
rs571689620	snp	A/G	0.00119737	0.0244387	intron-variant	DTX2	GRCh38.p7	7:76465147	GCACATCCAGGCATC[A/G]TGGGAAGTGCTGTTT	113878
rs571723258	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505903	CCTGGTGTGGGGCGA[A/G]TAGAGACTTCCCCAG	113878
rs571750184	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76475105	TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA	113878
rs571843846	snp	A/G			intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76476580	CGTGCACACAAGGGT[A/G]GGTGGAGCCAGCCGT	113878
rs571930156	snp	A/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76490643	TTTTTTGACAGAGTC[A/T]CCAGCCTGGGCTGGA	113878
rs571968762	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76501076	GAACCTGAACCTCTA[C/T]TGAGCCACGTTTTGG	113878
rs571986560	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501733	ATTCCTGTCTCCCTT[A/G]TAAGACCCCACGCCG	113878
rs572147706	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76491620	ACTAGTGAGTATAAA[A/G]TATCTTTTTTTTTCT	113878
rs572150355	snp	C/T	0.000642076	0.017906	intron-variant	DTX2	GRCh38.p7	7:76492269	GTAGGTGCCTGACCT[C/T]GGGCTGCAGAGCAGT	113878
rs572238814	snp	C/T	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76481705	ATGCTGCTCGCCATC[C/T]GGCAGTGCACTGGGC	113878
rs572274639	snp	A/G	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76481156	CCTCTGCATGTGTGC[A/G]TTTCTGCTTTTTGGT	113878
rs572287651	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76464591	ATCTAGAGACAGTGC[C/T]GCTCTACGTTGTCCA	113878
rs572320128	snp	C/T	0.00119737	0.0244387	intron-variant	DTX2	GRCh38.p7	7:76465256	GGGTGGGGACAGACA[C/T]GCTGATGCACATGGG	113878
rs572400442	snp	G/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474614	CTCACATATTGTTAA[G/T]TTGAAAGTAGCCGTG	113878
rs572450293	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76482430	TTTGTTTATTTTGGC[A/G]GTTGAAAAAAGAATT	113878
rs572583548	snp	A/C	0.00478085	0.0486577	intron-variant	DTX2	GRCh38.p7	7:76494955	ACGAGCGTTTGCGCA[A/C]AGGCTTTTTGCAGAG	113878
rs572684272	snp	C/T	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76483586	AAGGGGCTGTCAGCG[C/T]GGTGTGAGGGAGGGC	113878
rs572695730	snp	G/T	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76495778	AGCAGGAGTCCAGCA[G/T]GGTGGGGCGGGAGGC	113878
rs572867335	snp	A/G	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76479924	CGGTACGTAGGCTGC[A/G]GGATTGACTTTGAAT	113878
rs572932122	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76499958	GTGTGGCGGTCGGCG[C/T]GTGTGCAGCTGCCTG	113878
rs572967098	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76504533	ACTCTGCTTCTGCAG[C/T]GGAGGACAGAGGCTG	113878
rs573134039	snp	A/G	0.000555556	0.0166574	missense	DTX2	GRCh38.p7	7:76500483	CAGAGCAGGTCATAA[A/G]AAACTACACGGAAGA	113878
rs573286227	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471763	TTTGCCCTCTGGGTA[A/G]GCCCGTAAACCAGGG	113878
rs573392687	in-del	-/AGG	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76475593	TTGGGAGGCTGCAGC[-/AGG]AGAACTGCTTGAACC	113878
rs573674553	snp	A/C	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76504543	TGCAGCGGAGGACAG[A/C]GGCTGAGGCCGGGCC	113878
rs573684223	in-del	-/G	0.0023933	0.0345097	intron-variant	DTX2	GRCh38.p7	7:76499525	GCCCCTTCTGGTCCT[-/G]GGAGTCTGGGACGAC	113878
rs573777097	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	DTX2	GRCh38.p7	7:76463480	ATCCAACATCTGTAC[C/T]TTTGTTTTTACTAAC	113878
rs573861778	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76500972	TCGCCCAGGCTCAGT[A/G]CAGTGGCGTGATCAC	113878
rs573891853	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505948	GGTTCTGGGTCAGCT[G/T]CTTTTACCTCAATTT	113878
rs573906870	snp	G/T	0.0640965	0.167152	intron-variant	DTX2	GRCh38.p7	7:76500613	TGCTTGAAGGGTGCT[G/T]CCCAGGTGCCTCTGG	113878
rs573914414	snp	C/T			intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76479613	GGTGAAACCCCGTCT[C/T]TACTAAAAATACAAA	113878
rs573987031	snp	C/T	0.00597247	0.0543191	utr-variant-5-prime, upstream-variant-2KB	DTX2	GRCh38.p7	7:76480449	GCTGGGCAATGACCC[C/T]GGGACTCCAGGCCAG	113878
rs574188604	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76468080	ATGGAGAGAGGAGGG[A/G]AGGAGGGGAGAGGGA	113878
rs574209580	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	DTX2	GRCh38.p7	7:76506453	GCAAAATTGCAAGAC[C/T]TCATCTCTAAAAAAA	113878
rs574222544	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-5-prime	DTX2	GRCh38.p7	7:76477067	GACACCCAGGAGTAA[C/T]TGGCTTGGAAGGCAG	113878
rs574506211	snp	C/G	0.0166325	0.0896639	intron-variant	DTX2	GRCh38.p7	7:76467106	GCTTCACTGTGTTGC[C/G]CAGGCTGGTCTTGAA	113878
rs574515440	snp	G/T	0.0349115	0.127424	intron-variant	DTX2	GRCh38.p7	7:76503781	GGGTAAGCTCTTAGG[G/T]CTGTGGCAGCAAAAG	113878
rs574724171	snp	G/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76498062	AACCTTTCCCAAGCG[G/T]GTGCTGGCCCTGCTT	113878
rs574880002	snp	C/T	0.00159617	0.0282053	intron-variant	DTX2	GRCh38.p7	7:76483695	GCCTGGTAGAGCGCT[C/T]AGCTCCTTGAGAGAG	113878
rs574897019	snp	A/G	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76502816	CCTTACAGCATCCCT[A/G]TGCAGTCAGCACAGT	113878
rs575055001	snp	C/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB, utr-variant-5-prime	DTX2	GRCh38.p7	7:76479041	GCTGTGAATGAAGCA[C/G]GCTTGGGGTTGCTGC	113878
rs575057013	snp	C/T	0.00676609	0.0577691	intron-variant, downstream-variant-500B	DTX2, FDPSP2	GRCh38.p7	7:76469688	GTGAGCCACTGAGCC[C/T]GGCCAAATATTCCAA	113878
rs575094745	snp	A/G	0.095934	0.196885	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76478229	gacgtcctcatagtc[A/G]catggcttgtgaTAA	113878
rs575144031	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76477194	GTCTGATCTTCGGGG[C/T]AGGTTGTGGGCTTTT	113878
rs575190984	snp	A/G	0.00119737	0.0244387	intron-variant	DTX2	GRCh38.p7	7:76498143	AGTGGGCGTGGTGGC[A/G]GGCAGGGAGGGTGGC	113878
rs575219088	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76486270	TAGTAAATACCTGAC[C/T]TCTTAACCTAGCAGG	113878
rs575237020	snp	A/T	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76483899	TCTCCACAAAAAAAA[A/T]TTTTTTAATTAGCCA	113878
rs575237115	snp	C/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76499609	GTGGCACTGGGCTCC[C/G]CGTCCCTCTTTCACC	113878
rs575243749	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76470934	GCATCCAGTTTCCTC[A/G]GCTCCACCAGCTCCC	113878
rs575324213	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76503881	TCTGGGCAGAAGGGC[A/G]GGCAGTTCAGTGGGA	113878
rs575536087	snp	A/G	0.00252157	0.0354179	intron-variant	DTX2	GRCh38.p7	7:76504493	GGGCCCTGACCAGGC[A/G]GCAGGAGGCCAGGCG	113878
rs575656254	snp	A/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502237	GCCTCTTTTTCCAAG[A/T]CTGGCCCACGTCAGC	113878
rs575761949	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471057	GTCTCTGGGTGCCCC[A/G]TCTCATCCTCAGTCA	113878
rs575769091	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471560	AAGAGACAGGGTCTC[A/G]CTCTGTTGCCCAGGT	113878
rs575972607	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76491835	CGCACCACCACACTT[A/G]GCAGACTTTTAAAAA	113878
rs575978281	snp	C/G	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76492364	CAGGGAGAGCCAAAG[C/G]GGCTCCCTGGGGGAG	113878
rs576128692	snp	A/G	0.0726307	0.176182	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76475243	TTGAACCCGGGAGGC[A/G]GAGGTTGCAGTGAGC	113878
rs576133790	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76481759	GGCCCACAGTGTCAC[C/T]AGTGAGGAAACTTGA	113878
rs576257603	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76464756	GGTTTAGACTGGATT[A/G]TTCGCTTTGTGGCGG	113878
rs576312867	snp	A/G			intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76479860	AAAGAAGCTGGGCTG[A/G]TGACTAGCACCCGGA	113878
rs576313480	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474749	CTCACAGCTGGGCAG[A/G]GTGATTTCCACTCAA	113878
rs576395958	snp	C/T	0.0126979	0.078662	intron-variant	DTX2	GRCh38.p7	7:76482274	CTAAGGCAGGAGGAT[C/T]GCTTGAGCCCAGGAG	113878
rs576430862	snp	C/T	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76494859	GCCTGGCCAGCACCC[C/T]GGAGCCAGAGCTGGA	113878
rs576502359	snp	C/T	0.00159617	0.0282053	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502619	TTCTAAAGGCCTGGC[C/T]GGCTCTCCTAGGCCT	113878
rs576563961	snp	A/G	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76503043	ACCGAGTCATGTGGC[A/G]CATCGGAGCCTGGCT	113878
rs576694832	snp	A/G	1.65272e-05	0.0028746	intron-variant	DTX2	GRCh38.p7	7:76497287	TCACATGCCGAAGGA[A/G]TCTTCTAATGTCTCT	113878
rs576710616	snp	A/G	1.66416e-05	0.00288453	missense	DTX2	GRCh38.p7	7:76483026	GCGCCCAGGCTGAAC[A/G]CCACCAACGCCTGGG	113878
rs576723507	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76476813	CTGGTCATGGAGGGG[C/T]TTGTGTGCCTTGTCA	113878
rs576853161	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76476515	GTTTTGGTGGGGAGA[A/C]GGCCACTGAAACCAG	113878
rs576853919	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76496028	ACATTCAGTTCCCAC[A/G]GGAACCGCATTTGAG	113878
rs576857970	snp	A/G	0.0832709	0.186283	intron-variant	DTX2	GRCh38.p7	7:76466268	CTAAGCTGAGAACAA[A/G]ATTGATTAGTACACA	113878
rs577144022	snp	A/G	0.000153142	0.00874915	intron-variant	DTX2	GRCh38.p7	7:76503382	GTGACGGTCTTGGGT[A/G]TTCTCAGACTGCCAG	113878
rs577458937	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	DTX2, FDPSP2	GRCh38.p7	7:76469612	ATTAGCCAGGATGGT[C/G]TCGCTCTCCTGACCT	113878
rs577480934	snp	A/G	0.0158469	0.0875917	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76477231	GGAATTGGCAGCTCC[A/G]TGGCGGGCCTGGCAC	113878
rs577518480	snp	A/C/T	3.5204e-05	0.00419535	missense	DTX2	GRCh38.p7	7:76483129	TGCCCCCAGGATCCT[A/C/T]CACCTCCGGTGCAGT	113878
rs577589087	snp	G/T	0.000399281	0.0141238	utr-variant-5-prime, intron-variant	DTX2	GRCh38.p7	7:76463685	CCAGAAGGGACAGTT[G/T]GTGCCAGCTCTCCAG	113878
rs577639787	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76477968	GGCCCATTTTCTTAG[C/G]TAGGAGGGCTCAGTC	113878
rs577726843	snp	A/G	2.48284e-05	0.00352329	utr-variant-5-prime, upstream-variant-2KB	DTX2	GRCh38.p7	7:76480466	GGACTCCAGGCCAGA[A/G]GGGTCTGAAGCTGTT	113878
rs577753765	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76464394	GCCATGCCAAGACTC[A/G]GGAGTGGAAGGATTT	113878
rs577848714	in-del	-/C	0.00119737	0.0244387	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474734	TCACCCGCCCCGGGG[-/C]TCACAGCTGGGCAGG	113878
rs577851659	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76501036	TAATGAACAGGACCA[A/G]TCAGACTCCTGTTGC	113878
rs577857102	snp	C/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474146	GGCTGGTCTCAAACT[C/G]CCGACCTCAGGTGAT	113878
rs577878052	snp	C/T	0.00159617	0.0282053	intron-variant	DTX2	GRCh38.p7	7:76491447	TGTGTGCCAGCATGC[C/T]CAGCTAATTTTTTAT	113878
rs577914930	snp	A/C	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76490336	TCCCCTCACCCCCCC[A/C]AAAAAAGAAAATTAC	113878
rs577997574	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505979	TGTTTGCAATAAATG[C/G]TCTATAGCCAAAGCC	113878
rs578023908	snp	A/C			intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474353	AGCCACCACGCTTGG[A/C]CTGTTTTACATGTTG	113878
rs578105583	snp	A/G	1.68457e-05	0.00290216	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502273	CCACTGTTGGCGAGC[A/G]TGACCCATGTTTGGT	113878
rs578218650	snp	A/G	3.88871e-05	0.00440931	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502499	GGGTGGCCCGCCCCC[A/G]CAGTCCTGAGCTGTC	113878
rs745337399	snp	G/T	1.6834e-05	0.00290116	missense, downstream-variant-500B	DTX2	GRCh38.p7	7:76502302	GTCTCCTCCAGGACT[G/T]CATCATCTGCATGGA	113878
rs745376129	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76481290	CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG	113878
rs745386317	snp	C/T	8.29772e-05	0.00644063	missense	DTX2	GRCh38.p7	7:76483015	GGGCCCGGTCTGCGC[C/T]CAGGCTGAACACCAC	113878
rs745488629	snp	A/G	2.78129e-05	0.00372903	missense	DTX2	GRCh38.p7	7:76505471	CCGTGGTATGGAACG[A/G]GATCCACCACAAGAC	113878
rs745621522	snp	A/G	0.000251124	0.0112026	missense, intron-variant	DTX2	GRCh38.p7	7:76503537	TCGCTCCCCGGCCAC[A/G]AGGACTGCGGGACCA	113878
rs745654588	in-del	-/GA			intron-variant	DTX2	GRCh38.p7	7:76483703	AGCGCTCAGCTCCTT[-/GA]GAGAGAGAGAGAATG	113878
rs745674937	snp	C/T	0.000115956	0.00761346	missense, intron-variant	DTX2	GRCh38.p7	7:76497369	ATGTCAGCCATTGGA[C/T]TCCCTGTGTGTCTTA	113878
rs745692855	snp	A/G	1.71076e-05	0.00292464	intron-variant	DTX2	GRCh38.p7	7:76503592	ATGGTATCCAGGTGA[A/G]GGGCCTTCTTGAGTC	113878
rs745791636	snp	C/T	1.8014e-05	0.00300111	missense	DTX2	GRCh38.p7	7:76480739	TGGCCCCTTACATTA[C/T]TGACCTCCCCAGCTG	113878
rs745845061	snp	C/T	0.000393921	0.0140287	intron-variant	DTX2	GRCh38.p7	7:76480814	GCACATATCTGGGTG[C/T]CGCACCTGCTTTCCC	113878
rs746041371	in-del	-/C			intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471252	CTGCAAACTCCACTT[-/C]CTGGGTTCACGCCAT	113878
rs746131098	snp	C/T	0.00015749	0.00887244	synonymous-codon	DTX2	GRCh38.p7	7:76480557	GGTGTACACCAGCCC[C/T]GCGGCTGTGGCCGTG	113878
rs746249602	snp	C/G	1.66568e-05	0.00288585	missense	DTX2	GRCh38.p7	7:76482676	AGCTCGTGGACTTGG[C/G]CCCCCTGGGGTACAA	113878
rs746295240	snp	G/T	4.17336e-05	0.00456783	missense	DTX2	GRCh38.p7	7:76505425	CTCATCTTCACAGTG[G/T]GCACGTCCAGCACCA	113878
rs746371706	snp	A/G	3.93136e-05	0.00443342	missense	DTX2	GRCh38.p7	7:76492217	ACTGTGCCCATGCAG[A/G]TGCCAAAGCCCAGCA	113878
rs746424742	snp	A/G	1.65239e-05	0.00287431	intron-variant	DTX2	GRCh38.p7	7:76497295	CGAAGGAGTCTTCTA[A/G]TGTCTCTCCCTCTCT	113878
rs746434863	snp	C/G	0.000330376	0.0128483	synonymous-codon	DTX2	GRCh38.p7	7:76482599	GAGCGACGATGGCTC[C/G]TGGACTGCCTATGAA	113878
rs746479588	snp	C/T	1.72606e-05	0.00293768	missense	DTX2	GRCh38.p7	7:76483089	CTCTACCGCTCCAGC[C/T]TCTCCCACCTGGGAC	113878
rs746534819	snp	C/T	3.15721e-05	0.00397304	intron-variant	DTX2	GRCh38.p7	7:76480817	CATATCTGGGTGCCG[C/T]ACCTGCTTTCCCACA	113878
rs746560210	snp	A/G			downstream-variant-500B	DTX2	GRCh38.p7	7:76506207	TCTCCCTGCCATGCC[A/G]GAGGCTGTCACCCCA	113878
rs746628260	snp	A/G	1.67908e-05	0.00289743	missense, downstream-variant-500B	DTX2	GRCh38.p7	7:76502364	GTGACTGACAGCAAG[A/G]CAATCGGGTCCCTAG	113878
rs746680101	snp	A/G			utr-variant-3-prime	DTX2	GRCh38.p7	7:76505779	TCCTCCCCTCTGGGA[A/G]TTGGGCAGCCCTGGG	113878
rs746734108	snp	A/G	0.000104961	0.00724359	missense, intron-variant	DTX2	GRCh38.p7	7:76497442	CTTCCAAAAGTCACG[A/G]CTCAGTTAAGAGATT	113878
rs746771647	snp	C/T	8.37889e-05	0.00647205	missense	DTX2	GRCh38.p7	7:76504407	GCCAGAGGGTTTCCC[C/T]GCCAGTGCTACCTTC	113878
rs746824999	snp	C/T	0.000673741	0.0183417	intron-variant	DTX2	GRCh38.p7	7:76500346	TCTCGCATTTCCTCC[C/T]GGCAGCTTAGACCTC	113878
rs746889603	snp	G/T	1.72928e-05	0.00294043	intron-variant	DTX2	GRCh38.p7	7:76503605	GAGGGGCCTTCTTGA[G/T]TCCCCCACTCCTGGC	113878
rs746907828	snp	A/C	1.64738e-05	0.00286995	synonymous-codon	DTX2	GRCh38.p7	7:76482509	TCCTTTGAAAATAGG[A/C]ACCATGCGGGCTGTG	113878
rs747104897	snp	C/T	3.30147e-05	0.00406279	intron-variant	DTX2	GRCh38.p7	7:76497309	AATGTCTCTCCCTCT[C/T]TGCGTGTCTGCTCTC	113878
rs747125833	snp	C/G/T	3.34825e-05	0.00409149	missense, intron-variant	DTX2	GRCh38.p7	7:76503528	TTCCAGATGTCGCTC[C/G/T]CCGGCCACGAGGACT	113878
rs747239083	snp	C/G	5.22826e-05	0.00511259	missense	DTX2	GRCh38.p7	7:76480716	CTTGGGCCAGGCAGA[C/G]CCCTCGCTGGCCCCT	113878
rs747244729	snp	C/T	8.43832e-05	0.00649496	synonymous-codon	DTX2	GRCh38.p7	7:76480635	CGTCTGCAGCTTCAT[C/T]GAGCAGCAGTTTGTC	113878
rs747246711	in-del	-/TG	3.49718e-05	0.00418147	intron-variant	DTX2	GRCh38.p7	7:76492286	GGCTGCAGAGCAGTC[-/TG]TGCCCTGCGGACTTG	113878
rs747339432	snp	C/T	0.000390376	0.0139655	missense	DTX2	GRCh38.p7	7:76505507	TGGACCGCAACATTA[C/T]GGGCCACGGCTATCC	113878
rs747510336	snp	A/C	0.000133213	0.00816021	synonymous-codon	DTX2	GRCh38.p7	7:76482680	CGTGGACTTGGCCCC[A/C]CTGGGGTACAACTAC	113878
rs747544596	snp	A/G	1.65042e-05	0.0028726	missense, intron-variant	DTX2	GRCh38.p7	7:76497354	ATGACGAGTGTTCTG[A/G]TGTCAGCCATTGGAC	113878
rs747565446	snp	A/G	4.96323e-05	0.00498133	missense	DTX2	GRCh38.p7	7:76482753	AGCTTCTGCCGCAGC[A/G]TGCGGCGCCAAGCAG	113878
rs747694774	snp	A/G	6.61934e-05	0.00575259	missense	DTX2	GRCh38.p7	7:76482570	CCTGGCCGAGGTGTC[A/G]TCTGGGAGTGGCTGA	113878
rs747797686	in-del	-/A			downstream-variant-500B	DTX2	GRCh38.p7	7:76506439	GAGACCAGCCTGAGC[-/A]AAAATTGCAAGACCT	113878
rs747801084	snp	C/G	3.57213e-05	0.00422604	intron-variant	DTX2	GRCh38.p7	7:76483167	CGTGGGCAACGGCCG[C/G]TCGTTTTGTCTGCCC	113878
rs747856154	snp	C/T	3.92981e-05	0.00443255	missense	DTX2	GRCh38.p7	7:76492163	CCCAGTGCCTCCCTC[C/T]CCAGCGGTCCCTCAA	113878
rs747887912	snp	A/G	0.000165412	0.00909279	intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501302	AATCTGGTAAGTAAA[A/G]GTTTGGAAAGGAGCC	113878
rs747982040	snp	A/G	1.6495e-05	0.0028718	missense	DTX2	GRCh38.p7	7:76482942	CCCCCACACAGGACC[A/G]CTTCTGTGTTTGGGA	113878
rs748045715	snp	C/T	0.000235988	0.0108599	intron-variant	DTX2	GRCh38.p7	7:76500376	CTTCCTTCCCTTCCT[C/T]GCCCTCTGGCCTCCT	113878
rs748045937	snp	A/C	1.66649e-05	0.00288655	splice-acceptor-variant	DTX2	GRCh38.p7	7:76505372	TCCTCCTCCCCGGGC[A/C]GGTCCTAGAGCTCCT	113878
rs748124114	snp	A/G	1.65157e-05	0.0028736	missense, intron-variant	DTX2	GRCh38.p7	7:76497363	GTTCTGATGTCAGCC[A/G]TTGGACTCCCTGTGT	113878
rs748256743	snp	C/T	5.49451e-05	0.00524114	intron-variant	DTX2	GRCh38.p7	7:76480800	GCTGTCTGCCTCTCG[C/T]ACATATCTGGGTGCC	113878
rs748260034	snp	A/C	1.70406e-05	0.0029189	missense, intron-variant	DTX2	GRCh38.p7	7:76497418	CCAGCCCTCCCGCCT[A/C]CCGTCTGGCTTCCAA	113878
rs748418088	snp	C/T	8.21659e-05	0.00640907	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505803	CCCTGGGCAGTTGTA[C/T]TCATGGGGGCTTAGG	113878
rs748763928	snp	A/G	3.017e-05	0.00388382	missense	DTX2	GRCh38.p7	7:76505458	GGTGAGACGGACACC[A/G]TGGTATGGAACGAGA	113878
rs748780379	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76503134	TGCAAGGCTGTCTAT[C/T]CGACTGCAAATGCGA	113878
rs748903280	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76483413	CCTCCACATGGAGCA[A/G]AGTTAAAGGCCTGTG	113878
rs748933743	snp	C/T	6.60971e-05	0.00574841	synonymous-codon	DTX2	GRCh38.p7	7:76482590	GGAGTGGCTGAGCGA[C/T]GATGGCTCCTGGACT	113878
rs748984492	in-del	-/T	0.000102049	0.0071424	frameshift-variant, intron-variant	DTX2	GRCh38.p7	7:76497410	CCAGCCCACCAGCCC[-/T]CCCGCCTCCCGTCTG	113878
rs748985178	snp	A/G	3.32209e-05	0.00407546	missense	DTX2	GRCh38.p7	7:76482666	AGGGGCAACCAGCTC[A/G]TGGACTTGGCCCCCC	113878
rs749198761	in-del	-/TG			downstream-variant-500B	DTX2	GRCh38.p7	7:76506409	AGACAGGAGGCTCAC[-/TG]TAGTCCAGACATTTG	113878
rs749222258	snp	C/G	1.68499e-05	0.00290253	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502289	TGACCCATGTTTGGT[C/G]TCCTCCAGGACTGCA	113878
rs749268963	snp	A/G	1.65729e-05	0.00287857	missense	DTX2	GRCh38.p7	7:76483006	CACTCTCCGGGGCCC[A/G]GTCTGCGCCCAGGCT	113878
rs749409113	snp	C/T	8.24491e-05	0.0064201	synonymous-codon	DTX2	GRCh38.p7	7:76482887	AGGCCGCTACCGCCA[C/T]TCCATGACCAACCTC	113878
rs749612129	snp	G/T	1.80843e-05	0.00300696	intron-variant	DTX2	GRCh38.p7	7:76483184	CGTTTTGTCTGCCCT[G/T]TGTTTCCGCTCTTAG	113878
rs749615626	snp	A/G	5.0119e-05	0.0050057	synonymous-codon	DTX2	GRCh38.p7	7:76492186	TCCCTCAAGCAGCCC[A/G]GGGAGCGTCCCTGCC	113878
rs749712313	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76481047	GAAGGGTTCCTTTGG[C/T]CGGCAGGCCGGCATG	113878
rs749746176	snp	A/C	1.76736e-05	0.00297262	missense	DTX2	GRCh38.p7	7:76480550	TGGTGCAGGTGTACA[A/C]CAGCCCCGCGGCTGT	113878
rs749904794	snp	A/G	0.000181663	0.00952882	missense	DTX2	GRCh38.p7	7:76505578	GCCCAGGGGGTGACC[A/G]AGGACTGCCTGGAGC	113878
rs749972814	snp	C/T	0.287396	0.247187	synonymous-codon	DTX2	GRCh38.p7	7:76482866	CAGCAGAACTGGCCC[C/T]GTGTCAGGCCGCTAC	113878
rs750062248	snp	C/G	1.69023e-05	0.00290704	missense, intron-variant	DTX2	GRCh38.p7	7:76497400	GCCGCGCACCCCAGC[C/G]CACCAGCCCTCCCGC	113878
rs750077248	snp	A/G	4.96438e-05	0.00498191	missense	DTX2	GRCh38.p7	7:76482748	CTTCCAGCTTCTGCC[A/G]CAGCGTGCGGCGCCA	113878
rs750216576	snp	C/T	0.000136218	0.0082517	intron-variant	DTX2	GRCh38.p7	7:76492118	TTTCCAATAAGTCAG[C/T]GGTGTGCAGTAAGCT	113878
rs750239426	snp	A/C/G/T	5.30775e-05	0.00515135	intron-variant	DTX2	GRCh38.p7	7:76482505	GTTTTCCTTTGAAAA[A/C/G/T]AGGCACCATGCGGGC	113878
rs750308075	snp	A/C	2.14323e-05	0.00327348	utr-variant-5-prime, upstream-variant-2KB	DTX2	GRCh38.p7	7:76480501	AAAGCAGCGGGACTC[A/C]TTGGGAAGATGGCCA	113878
rs750414249	snp	A/T	1.78077e-05	0.00298388	intron-variant	DTX2	GRCh38.p7	7:76483159	TCAGGTATCGTGGGC[A/T]ACGGCCGCTCGTTTT	113878
rs750563156	snp	C/T	1.65411e-05	0.00287581	missense	DTX2	GRCh38.p7	7:76482994	ACAACAAACCCTCAC[C/T]CTCCGGGGCCCGGTC	113878
rs750652106	snp	A/G	3.3543e-05	0.00409516	missense	DTX2	GRCh38.p7	7:76505444	CGTCCAGCACCACGG[A/G]TGAGACGGACACCGT	113878
rs750705032	snp	A/C	3.37092e-05	0.0041053	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502278	GTTGGCGAGCATGAC[A/C]CATGTTTGGTCTCCT	113878
rs750788526	snp	A/G	1.67416e-05	0.00289318	missense, intron-variant	DTX2	GRCh38.p7	7:76503558	TGCGGGACCATCCTC[A/G]TAGTTTACAGCATTC	113878
rs750818736	snp	C/T	1.65004e-05	0.00287227	synonymous-codon, intron-variant	DTX2	GRCh38.p7	7:76497347	TGCAGGCATGACGAG[C/T]GTTCTGATGTCAGCC	113878
rs750902333	snp	C/T	3.4534e-05	0.00415521	missense	DTX2	GRCh38.p7	7:76480699	CTGGCCCACAGCATC[C/T]CCTTGGGCCAGGCAG	113878
rs750978103	snp	A/C	1.67399e-05	0.00289304	missense, intron-variant	DTX2	GRCh38.p7	7:76503519	GTATTACGGTTCCAG[A/C]TGTCGCTCCCCGGCC	113878
rs751041788	snp	A/G	6.64945e-05	0.00576566	missense	DTX2	GRCh38.p7	7:76480777	TTCCGCCAGGACACC[A/G]GTAAGACGCTGTCTG	113878
rs751050295	snp	A/G	3.42179e-05	0.00413615	missense	DTX2	GRCh38.p7	7:76480586	TGTGGGAATGGCAGG[A/G]CGGGCTGGGCACCTG	113878
rs751064400	snp	A/T	1.69315e-05	0.00290955	missense, downstream-variant-500B	DTX2	GRCh38.p7	7:76502412	AAGTGCAGCCATGCC[A/T]TCCACCTGCTGTGCC	113878
rs751117493	snp	C/T	9.20853e-05	0.00678485	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502483	GGCCCAGGGCGGAGG[C/T]GGGTGGCCCGCCCCC	113878
rs751158935	snp	C/T	4.95201e-05	0.0049757	missense	DTX2	GRCh38.p7	7:76482876	GGCCCCGTGTCAGGC[C/T]GCTACCGCCACTCCA	113878
rs751208016	in-del	-/ATTTTTTTTTTT			intron-variant	DTX2	GRCh38.p7	7:76468448	ATCTGGCCCACTGCC[-/ATTTTTTTTTTT]TTTTTTTTTTTTTTT	113878
rs751283284	snp	C/T	1.64781e-05	0.00287033	missense	DTX2	GRCh38.p7	7:76480529	CCATGGCCCCAAGCC[C/T]TTCCCTGGTGCAGGT	113878
rs751323273	snp	C/G	8.1616e-05	0.00638759	intron-variant	DTX2	GRCh38.p7	7:76505365	TTCCCCCTCCTCCTC[C/G]CCGGGCAGGTCCTAG	113878
rs751532127	snp	A/G	0.000100629	0.00709256	intron-variant	DTX2	GRCh38.p7	7:76492122	CAATAAGTCAGCGGT[A/G]TGCAGTAAGCTCTGC	113878
rs751557710	snp	C/T	1.66037e-05	0.00288125	stop-gained	DTX2	GRCh38.p7	7:76482561	CACTCAGCCCCTGGC[C/T]GAGGTGTCGTCTGGG	113878
rs751685365	snp	C/T	4.90822e-05	0.00495365	intron-variant	DTX2	GRCh38.p7	7:76480787	ACACCGGTAAGACGC[C/T]GTCTGCCTCTCGCAC	113878
rs751720408	snp	A/G	1.65534e-05	0.00287688	missense	DTX2	GRCh38.p7	7:76483000	AACCCTCACTCTCCG[A/G]GGCCCGGTCTGCGCC	113878
rs751764209	snp	C/G	5.03166e-05	0.00501555	missense, downstream-variant-500B	DTX2	GRCh38.p7	7:76502338	TGTCCACAGCGTCTG[C/G]ATACAGCGATGTGAC	113878
rs751941616	snp	A/C	3.60737e-05	0.00424683	intron-variant	DTX2	GRCh38.p7	7:76482477	CTTGGGGATGCTAGC[A/C]GACTAACCTTTTGTT	113878
rs751953292	snp	A/G	0.00044082	0.0148397	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505690	GTGCCCAGCCCGAGA[A/G]GCTGGGAGGTTTGTT	113878
rs752001142	snp	A/T	1.6775e-05	0.00289607	missense, intron-variant	DTX2	GRCh38.p7	7:76503578	TTACAGCATTCCCCA[A/T]GGTATCCAGGTGAGG	113878
rs752053882	snp	C/G	1.70124e-05	0.00291649	missense, intron-variant	DTX2	GRCh38.p7	7:76497408	CCCCAGCCCACCAGC[C/G]CTCCCGCCTCCCGTC	113878
rs752152848	snp	A/C	2.11441e-05	0.0032514	intron-variant	DTX2	GRCh38.p7	7:76503636	CACTCCTCTTCCCAC[A/C]CCGCCCACATCCCAG	113878
rs752290730	snp	A/G	2.62264e-05	0.00362112	intron-variant	DTX2	GRCh38.p7	7:76492296	CAGTCTGTGCCCTGC[A/G]GACTTGGTGGGGAGG	113878
rs752323328	in-del	-/A			intron-variant	DTX2	GRCh38.p7	7:76501102	TTTGGGGGCTGCAGC[-/A]CCACTTTCCCCTGAT	113878
rs752344409	snp	G/T	3.6974e-05	0.00429949	intron-variant	DTX2	GRCh38.p7	7:76503404	GACTGCCAGCTCAGT[G/T]GGTTGCGTCTGCCTC	113878
rs752437258	snp	A/G	3.08494e-05	0.00392731	missense	DTX2	GRCh38.p7	7:76505455	ACGGGTGAGACGGAC[A/G]CCGTGGTATGGAACG	113878
rs752490534	snp	C/T	2.55555e-05	0.00357451	missense	DTX2	GRCh38.p7	7:76505528	ACGGCTATCCCGACC[C/T]CAACTACCTGCAGAA	113878
rs752490607	snp	C/T	5.05813e-05	0.00502872	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502281	GGCGAGCATGACCCA[C/T]GTTTGGTCTCCTCCA	113878
rs752627787	snp	A/G	1.64961e-05	0.00287189	intron-variant	DTX2	GRCh38.p7	7:76497331	TCTGCTCTCACACCC[A/G]TGCAGGCATGACGAG	113878
rs752744436	snp	C/T	1.66565e-05	0.00288583	synonymous-codon	DTX2	GRCh38.p7	7:76482707	CTACACTGTCAACTA[C/T]ACCACCCACACGCAG	113878
rs752751942	snp	A/G	1.67778e-05	0.00289631	synonymous-codon	DTX2	GRCh38.p7	7:76482536	TGTGCGGAGACACCT[A/G]TTCCCCCAGCACTCA	113878
rs752826429	in-del	-/C	1.65228e-05	0.00287422	frameshift-variant	DTX2	GRCh38.p7	7:76482863	TGGCAGCAGAACTGG[-/C]CCCGTGTCAGGCCGC	113878
rs752856351	snp	A/C	1.76817e-05	0.00297331	synonymous-codon	DTX2	GRCh38.p7	7:76483142	CTCCACCTCCGGTGC[A/C]GTCAGGTATCGTGGG	113878
rs753029476	snp	C/T	1.7939e-05	0.00299486	intron-variant	DTX2	GRCh38.p7	7:76482488	TAGCAGACTAACCTT[C/T]TGTTTTCCTTTGAAA	113878
rs753079365	snp	A/G	1.79677e-05	0.00299725	synonymous-codon	DTX2	GRCh38.p7	7:76480542	CCCTTCCCTGGTGCA[A/G]GTGTACACCAGCCCC	113878
rs753180358	snp	A/G	4.94809e-05	0.00497373	missense	DTX2	GRCh38.p7	7:76482883	TGTCAGGCCGCTACC[A/G]CCACTCCATGACCAA	113878
rs753236679	snp	A/G			downstream-variant-500B	DTX2	GRCh38.p7	7:76506107	GGCTCATCGGCTCCC[A/G]TTTGATAACTGAAGA	113878
rs753243070	in-del	-/CCT	9.57809e-05	0.00691963	intron-variant	DTX2	GRCh38.p7	7:76505355	CTCCTTCCTCTTCCC[-/CCT]CCTCCTCCCCGGGCA	113878
rs753457366	snp	A/G			downstream-variant-500B	DTX2	GRCh38.p7	7:76506176	GGCTGTGCGGCCTCC[A/G]CATGCCCTACACTGA	113878
rs753661686	snp	A/C	0.000121929	0.00780702	missense	DTX2	GRCh38.p7	7:76483078	GGAGCCAGCCCCTCT[A/C]CCGCTCCAGCCTCTC	113878
rs753742812	snp	C/T	1.65373e-05	0.00287548	synonymous-codon	DTX2	GRCh38.p7	7:76482791	TTACCCGGTGACCAC[C/T]ATCATCGCTCCGCCG	113878
rs753747000	in-del	-/GTTTCACCT			intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501427	TGGTGTGACTGGGCC[-/GTTTCACCT]GTTTCACCCCAGGCT	113878
rs753825018	snp	A/G	8.38891e-05	0.00647592	missense, downstream-variant-500B	DTX2	GRCh38.p7	7:76502349	TCTGGATACAGCGAT[A/G]TGACTGACAGCAAGG	113878
rs754003845	snp	A/G	1.66696e-05	0.00288696	synonymous-codon	DTX2	GRCh38.p7	7:76482551	GTTCCCCCAGCACTC[A/G]GCCCCTGGCCGAGGT	113878
rs754307157	in-del	-/CT			utr-variant-3-prime	DTX2	GRCh38.p7	7:76505754	GCTCCCCCTGCCTGC[-/CT]CTCTCTCCTCCTCCC	113878
rs754340583	snp	C/G	1.69746e-05	0.00291325	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502267	CCCAGCCCACTGTTG[C/G]CGAGCATGACCCATG	113878
rs754352385	in-del	-/TT	1.70054e-05	0.00291589	frameshift-variant	DTX2	GRCh38.p7	7:76480668	GCAGAAGGGCCAACG[-/TT]TTGGGCTTGGGAGCC	113878
rs754368794	snp	C/T	5.09351e-05	0.00504628	missense	DTX2	GRCh38.p7	7:76480598	AGGACGGGCTGGGCA[C/T]CTGGCACCCCTACAG	113878
rs754463201	snp	A/G	1.65179e-05	0.00287379	synonymous-codon	DTX2	GRCh38.p7	7:76482977	CCAGGCCTTTGCACC[A/G]TACAACAAACCCTCA	113878
rs754477568	snp	A/G	3.65851e-05	0.00427683	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502484	GCCCAGGGCGGAGGC[A/G]GGTGGCCCGCCCCCA	113878
rs754597098	snp	C/T	1.85225e-05	0.00304317	synonymous-codon	DTX2	GRCh38.p7	7:76480533	GGCCCCAAGCCCTTC[C/T]CTGGTGCAGGTGTAC	113878
rs754706871	snp	C/T	1.7002e-05	0.0029156	synonymous-codon, downstream-variant-500B	DTX2	GRCh38.p7	7:76502426	CTTCCACCTGCTGTG[C/T]CTCCTGGCCATGTAC	113878
rs754752737	snp	C/T	0.000320179	0.0126486	intron-variant	DTX2	GRCh38.p7	7:76505367	CCCCCTCCTCCTCCC[C/T]GGGCAGGTCCTAGAG	113878
rs754766592	snp	C/G	1.65449e-05	0.00287614	missense	DTX2	GRCh38.p7	7:76482633	AGCGTCTGTGACTAT[C/G]TGGAGCAGCAGGTGG	113878
rs754853252	snp	A/G	4.97558e-05	0.00498753	missense	DTX2	GRCh38.p7	7:76482562	ACTCAGCCCCTGGCC[A/G]AGGTGTCGTCTGGGA	113878
rs754969071	snp	C/T	5.42814e-05	0.00520939	intron-variant	DTX2	GRCh38.p7	7:76480798	ACGCTGTCTGCCTCT[C/T]GCACATATCTGGGTG	113878
rs755110367	in-del	-/TAAA			intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76477800	GTGAGACTCGGACTC[-/TAAA]TAAATAAATAAATAA	113878
rs755130056	snp	A/T	1.68026e-05	0.00289845	synonymous-codon	DTX2	GRCh38.p7	7:76483049	CGCCTGGGGCGCAGC[A/T]CCTCCTTCCCTGGGG	113878
rs755207175	snp	C/G	0.000104743	0.00723606	synonymous-codon	DTX2	GRCh38.p7	7:76480719	GGGCCAGGCAGACCC[C/G]TCGCTGGCCCCTTAC	113878
rs755226446	snp	A/C	2.05214e-05	0.00320317	intron-variant	DTX2	GRCh38.p7	7:76497502	GTTCCCAAAAGCTCT[A/C]TGGCCTTTGCTAAGC	113878
rs755233813	snp	A/C			intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76501989	CCCCCTGAGTTCAAG[A/C]GATTCTCTTGCCTCA	113878
rs755336068	snp	A/G			missense	DTX2	GRCh38.p7	7:76505493	CCACAAGACAGAGAT[A/G]GACCGCAACATTACG	113878
rs755346853	snp	A/G	0.00101989	0.0225589	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505736	GCCCCACCTGAAGCC[A/G]GGGCTCCCCCTGCCT	113878
rs755566999	in-del	-/GGCTTGGGAGCCTGGCCCACAGCATCC	1.70571e-05	0.00292032	cds-indel	DTX2	GRCh38.p7	7:76480673	AGGGCCAACGTTTTG[-/GGCTTGGGAGCCTGGCCCACAGCATCC]CCTTGGGCCAGGCAG	113878
rs755588244	snp	C/T	7.55601e-05	0.00614608	intron-variant	DTX2	GRCh38.p7	7:76492300	CTGTGCCCTGCGGAC[C/T]TGGTGGGGAGGAAAT	113878
rs755621540	snp	C/T	4.95937e-05	0.0049794	synonymous-codon	DTX2	GRCh38.p7	7:76482587	CTGGGAGTGGCTGAG[C/T]GACGATGGCTCCTGG	113878
rs755665034	snp	G/T	1.6615e-05	0.00288223	stop-gained	DTX2	GRCh38.p7	7:76505380	CCCGGGCAGGTCCTA[G/T]AGCTCCTGAAGGTGG	113878
rs755739783	snp	A/G	1.65762e-05	0.00287886	missense	DTX2	GRCh38.p7	7:76482652	AGCAGCAGGTGGCCA[A/G]GGGCAACCAGCTCGT	113878
rs755816487	snp	C/T	1.82944e-05	0.00302438	intron-variant	DTX2	GRCh38.p7	7:76503410	CAGCTCAGTGGGTTG[C/T]GTCTGCCTCTGTCAG	113878
rs755843135	snp	C/G	1.6855e-05	0.00290297	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502286	GCATGACCCATGTTT[C/G]GTCTCCTCCAGGACT	113878
rs755962712	in-del	-/A/AT/ATT/TT			intron-variant	DTX2	GRCh38.p7	7:76469361	GCTTGAAATCTAGAT[-/A/AT/ATT/TT]TTTTTTTTTTTTTTT	113878
rs755964572	in-del	-/GCT			intron-variant	DTX2	GRCh38.p7	7:76486849	CTGTTGTGGTGGGCT[-/GCT]GCTGCTGCTGCTGCT	113878
rs755973929	snp	C/T	1.67804e-05	0.00289653	synonymous-codon, downstream-variant-500B	DTX2	GRCh38.p7	7:76502345	AGCGTCTGGATACAG[C/T]GATGTGACTGACAGC	113878
rs756017195	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76492045	CAAGGAGCGTAAAAG[C/T]GCGAAGACACCTCAG	113878
rs756074116	snp	C/G/T	6.11663e-05	0.00552993	synonymous-codon	DTX2	GRCh38.p7	7:76505457	GGGTGAGACGGACAC[C/G/T]GTGGTATGGAACGAG	113878
rs756084900	snp	C/T	1.66449e-05	0.00288482	synonymous-codon	DTX2	GRCh38.p7	7:76482713	TGTCAACTACACCAC[C/T]CACACGCAGACCAAC	113878
rs756368645	snp	A/C			intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76480388	GGGCTACTGATGTGC[A/C]TTGGTAACTGCTCAT	113878
rs756390618	snp	C/G	3.29712e-05	0.00406011	missense	DTX2	GRCh38.p7	7:76482928	CCGTCCCCCAGCACC[C/G]CCCACACAGGACCGC	113878
rs756438614	snp	A/G	0.000102304	0.00715131	splice-donor-variant, intron-variant	DTX2	GRCh38.p7	7:76503588	CCCCATGGTATCCAG[A/G]TGAGGGGCCTTCTTG	113878
rs756457469	snp	C/T	1.7747e-05	0.00297879	synonymous-codon	DTX2	GRCh38.p7	7:76480548	CCTGGTGCAGGTGTA[C/T]ACCAGCCCCGCGGCT	113878
rs756693764	snp	C/T			intron-variant, utr-variant-5-prime	DTX2	GRCh38.p7	7:76477014	ACATACCCCGTGTGC[C/T]GATGATGGAGGCGGC	113878
rs756835652	snp	G/T	1.66167e-05	0.00288237	missense	DTX2	GRCh38.p7	7:76482672	AACCAGCTCGTGGAC[G/T]TGGCCCCCCTGGGGT	113878
rs756836378	snp	A/G	1.68275e-05	0.0029006	missense, downstream-variant-500B	DTX2	GRCh38.p7	7:76502299	TTGGTCTCCTCCAGG[A/G]CTGCATCATCTGCAT	113878
rs756977113	snp	C/T	1.73357e-05	0.00294407	missense	DTX2	GRCh38.p7	7:76483080	AGCCAGCCCCTCTAC[C/T]GCTCCAGCCTCTCCC	113878
rs757012199	snp	C/G	1.68454e-05	0.00290214	missense, downstream-variant-500B	DTX2	GRCh38.p7	7:76502379	GCAATCGGGTCCCTA[C/G]CTGTGGGCCACCTCA	113878
rs757097732	snp	C/T	2.76974e-05	0.00372128	intron-variant	DTX2	GRCh38.p7	7:76480802	TGTCTGCCTCTCGCA[C/T]ATATCTGGGTGCCGC	113878
rs757166814	snp	A/T	1.67761e-05	0.00289617	missense, downstream-variant-500B	DTX2	GRCh38.p7	7:76502350	CTGGATACAGCGATG[A/T]GACTGACAGCAAGGC	113878
rs757243367	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76493203	GTGCTGGGATTACAG[A/G]CATGAGCCACCGTGC	113878
rs757338585	snp	A/G	1.64898e-05	0.00287135	missense	DTX2	GRCh38.p7	7:76482891	CGCTACCGCCACTCC[A/G]TGACCAACCTCCCTG	113878
rs757340640	snp	C/T	5.26316e-05	0.00512962	missense	DTX2	GRCh38.p7	7:76500488	CAGGTCATAAAAAAC[C/T]ACACGGAAGAGCTGA	113878
rs757469796	snp	C/G	1.64866e-05	0.00287106	missense	DTX2	GRCh38.p7	7:76482930	GTCCCCCAGCACCCC[C/G]CACACAGGACCGCTT	113878
rs757523819	snp	A/C	1.71991e-05	0.00293245	missense	DTX2	GRCh38.p7	7:76480690	CTTGGGAGCCTGGCC[A/C]ACAGCATCCCCTTGG	113878
rs757576615	snp	C/T	0.00381921	0.0435318	intron-variant	DTX2	GRCh38.p7	7:76500233	AGCCGGGTCCCCGGA[C/T]GGTGGGACTGGGGAA	113878
rs757631975	snp	G/T	4.95831e-05	0.00497886	intron-variant	DTX2	GRCh38.p7	7:76497288	CACATGCCGAAGGAG[G/T]CTTCTAATGTCTCTC	113878
rs757686165	snp	G/T	1.6743e-05	0.0028933	synonymous-codon, intron-variant	DTX2	GRCh38.p7	7:76503512	GATGGAGGTATTACG[G/T]TTCCAGATGTCGCTC	113878
rs757749277	snp	A/C	0.000457127	0.0151114	missense	DTX2	GRCh38.p7	7:76480605	GCTGGGCACCTGGCA[A/C]CCCTACAGTGCCACC	113878
rs757925978	snp	C/T	0.000140138	0.00836954	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505727	GTGGGGTGTGCCCCA[C/T]CTGAAGCCGGGGCTC	113878
rs758145884	snp	A/G	0.000203355	0.0100815	intron-variant	DTX2	GRCh38.p7	7:76492119	TTCCAATAAGTCAGC[A/G]GTGTGCAGTAAGCTC	113878
rs758156975	snp	C/T	4.35606e-05	0.00466674	missense	DTX2	GRCh38.p7	7:76505584	GGGGTGACCGAGGAC[C/T]GCCTGGAGCAGCAGT	113878
rs758253915	snp	A/G	0.00134499	0.0258976	missense	DTX2	GRCh38.p7	7:76504377	GAGCACCCCAATCCC[A/G]GAAAGCCGTTCACTG	113878
rs758272689	snp	A/C	1.66654e-05	0.00288659	missense	DTX2	GRCh38.p7	7:76482553	TCCCCCAGCACTCAG[A/C]CCCTGGCCGAGGTGT	113878
rs758494603	in-del	-/C	4.94621e-05	0.00497279	frameshift-variant	DTX2	GRCh38.p7	7:76482925	CCCCGTCCCCCAGCA[-/C]CCCCCCACACAGGAC	113878
rs758570695	snp	C/T	1.68491e-05	0.00290245	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502279	TTGGCGAGCATGACC[C/T]ATGTTTGGTCTCCTC	113878
rs758610020	snp	A/C	1.72791e-05	0.00293926	missense	DTX2	GRCh38.p7	7:76480700	TGGCCCACAGCATCC[A/C]CTTGGGCCAGGCAGA	113878
rs758670196	snp	A/C	0.000165057	0.00908303	missense	DTX2	GRCh38.p7	7:76482933	CCCCAGCACCCCCCA[A/C]ACAGGACCGCTTCTG	113878
rs758703814	snp	A/G/T	3.30002e-05	0.00406192	missense, intron-variant	DTX2	GRCh38.p7	7:76497348	GCAGGCATGACGAGT[A/G/T]TTCTGATGTCAGCCA	113878
rs758827753	snp	C/T	1.69539e-05	0.00291147	missense, intron-variant	DTX2	GRCh38.p7	7:76497403	GCGCACCCCAGCCCA[C/T]CAGCCCTCCCGCCTC	113878
rs758838587	snp	C/T			downstream-variant-500B	DTX2	GRCh38.p7	7:76506109	CTCATCGGCTCCCAT[C/T]TGATAACTGAAGAAC	113878
rs758946621	snp	A/T	2.34849e-05	0.00342665	intron-variant	DTX2	GRCh38.p7	7:76480783	CAGGACACCGGTAAG[A/T]CGCTGTCTGCCTCTC	113878
rs759082773	snp	A/G	1.70113e-05	0.00291639	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502251	GACTGGCCCACGTCA[A/G]CCCAGCCCACTGTTG	113878
rs759160377	snp	A/C			intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474931	GACAGAGATTTGTGG[A/C]GAAGACCTGACGAGA	113878
rs759179506	snp	G/T	1.86712e-05	0.00305536	intron-variant	DTX2	GRCh38.p7	7:76503399	TCTCAGACTGCCAGC[G/T]CAGTGGGTTGCGTCT	113878
rs759267168	snp	A/G	1.66538e-05	0.00288559	missense	DTX2	GRCh38.p7	7:76482703	ACAACTACACTGTCA[A/G]CTACACCACCCACAC	113878
rs759313120	in-del	-/C			intron-variant	DTX2	GRCh38.p7	7:76500886	CAGGTGGCTGTCCTG[-/C]CCCCCCGGCTATTGG	113878
rs759360406	snp	C/G	4.94858e-05	0.00497398	intron-variant	DTX2	GRCh38.p7	7:76497322	CTCTGCGTGTCTGCT[C/G]TCACACCCGTGCAGG	113878
rs759568472	snp	C/T	3.52995e-05	0.00420101	synonymous-codon	DTX2	GRCh38.p7	7:76483136	AGGATCCTCCACCTC[C/T]GGTGCAGTCAGGTAT	113878
rs759574652	snp	A/G	1.7564e-05	0.0029634	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502465	CAATAAGGTGCCCCC[A/G]CTGGCCCAGGGCGGA	113878
rs759623433	snp	A/G	0.0095185	0.0683275	intron-variant	DTX2	GRCh38.p7	7:76483192	CTGCCCTGTGTTTCC[A/G]CTCTTAGCCGGGAAG	113878
rs759736162	snp	A/C/T	6.71686e-05	0.00579486	missense, downstream-variant-500B	DTX2	GRCh38.p7	7:76502377	AGGCAATCGGGTCCC[A/C/T]AGCTGTGGGCCACCT	113878
rs759751825	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76469131	TTACACATTGTTTAT[A/G]GTTGTTCTTGTGGTC	113878
rs759817310	snp	C/G	2.41946e-05	0.00347803	utr-variant-5-prime, upstream-variant-2KB	DTX2	GRCh38.p7	7:76480479	GAGGGGTCTGAAGCT[C/G]TTTGGGAAAGCAGCG	113878
rs759881389	snp	C/G	0.000109475	0.00739767	intron-variant	DTX2	GRCh38.p7	7:76505331	TGAGCCCCTCTCACT[C/G]TCCGTCCCCTCCTTC	113878
rs759912494	in-del	-/TCC	0.015189	0.0858125	intron-variant	DTX2	GRCh38.p7	7:76504345	TATCCTGGTGTCTGT[-/TCC]TCCCGCAGGGCCCTG	113878
rs759952236	snp	C/T	3.37935e-05	0.00411043	missense	DTX2	GRCh38.p7	7:76482525	ACCATGCGGGCTGTG[C/T]GGAGACACCTGTTCC	113878
rs760008191	snp	A/G	0.00025112	0.0112025	intron-variant	DTX2	GRCh38.p7	7:76500415	TGTGCTCCTCAGGAC[A/G]CTGCTTATGTACTTC	113878
rs760099339	in-del	-/T			intron-variant	DTX2	GRCh38.p7	7:76463345	GTTTGCTTTTTGTTG[-/T]TTTCTTCAACCATCT	113878
rs760164498	snp	C/T	1.64969e-05	0.00287196	synonymous-codon, intron-variant	DTX2	GRCh38.p7	7:76497338	TCACACCCGTGCAGG[C/T]ATGACGAGTGTTCTG	113878
rs760201680	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76502813	CTTCCTTACAGCATC[C/T]CTGTGCAGTCAGCAC	113878
rs760252180	in-del	-/TCC			intron-variant, cds-indel	DTX2	GRCh38.p7	7:76501671	TCCTCGTTCAGAACG[-/TCC]TCCTCCCTCTTCCGG	113878
rs760290601	snp	A/G	1.67494e-05	0.00289386	missense, intron-variant	DTX2	GRCh38.p7	7:76503546	GGCCACGAGGACTGC[A/G]GGACCATCCTCATAG	113878
rs760293276	snp	C/T	5.63788e-05	0.00530907	synonymous-codon	DTX2	GRCh38.p7	7:76480749	CATTATTGACCTCCC[C/T]AGCTGGACCCAGTTC	113878
rs760353589	in-del	-/CAC	1.68724e-05	0.00290446	cds-indel, downstream-variant-500B	DTX2	GRCh38.p7	7:76502393	AGCTGTGGGCCACCT[-/CAC]CAAGTGCAGCCATGC	113878
rs760370340	snp	A/G	1.71062e-05	0.00292451	synonymous-codon	DTX2	GRCh38.p7	7:76480680	ACGTTTTGGGCTTGG[A/G]AGCCTGGCCCACAGC	113878
rs760402246	snp	G/T	2.61393e-05	0.00361511	synonymous-codon	DTX2	GRCh38.p7	7:76505538	CGACCCCAACTACCT[G/T]CAGAACGTGCTGGCT	113878
rs760456971	snp	A/G	4.13693e-05	0.00454785	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505640	TCTGGTGGCCACCCC[A/G]CTGCCCCATGGCTGG	113878
rs760550523	snp	C/T	1.65274e-05	0.00287462	missense	DTX2	GRCh38.p7	7:76482829	CAGGCGTCGCCTGCT[C/T]TTGCCACCAGTGCCT	113878
rs760631730	snp	C/T	8.3515e-05	0.00646146	missense, intron-variant	DTX2	GRCh38.p7	7:76497387	CCTGTGTGTCTTAGC[C/T]GCGCACCCCAGCCCA	113878
rs760653490	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76505004	TGGCGGAGCTGGAGG[C/T]GGGGAGAGGGCAGGG	113878
rs760694781	snp	A/C	1.67497e-05	0.00289389	missense	DTX2	GRCh38.p7	7:76482540	CGGAGACACCTGTTC[A/C]CCCAGCACTCAGCCC	113878
rs760696777	snp	C/T	6.56858e-05	0.00573049	stop-gained	DTX2	GRCh38.p7	7:76492241	CCCAGCAGAGTCCAG[C/T]AGGCGCTCGCAGGTA	113878
rs760749861	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76500869	AAGTGAGGTGGCCTC[A/G]TCCAGGTGGCTGTCC	113878
rs760758112	snp	A/C	1.65293e-05	0.00287479	missense	DTX2	GRCh38.p7	7:76482616	GGACTGCCTATGAAG[A/C]CAGCGTCTGTGACTA	113878
rs760921023	snp	G/T	3.97243e-05	0.00445652	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502507	CGCCCCCACAGTCCT[G/T]AGCTGTCCCCTGCAG	113878
rs760961897	snp	C/T			downstream-variant-500B	DTX2	GRCh38.p7	7:76506022	GTGTGTGCATGCATG[C/T]GTGTGTGCGCACTTG	113878
rs761113916	snp	C/T	1.65141e-05	0.00287346	missense	DTX2	GRCh38.p7	7:76482975	CACCAGGCCTTTGCA[C/T]CGTACAACAAACCCT	113878
rs761188367	snp	C/T	0.000117281	0.00765682	synonymous-codon, intron-variant	DTX2	GRCh38.p7	7:76497389	TGTGTGTCTTAGCCG[C/T]GCACCCCAGCCCACC	113878
rs761242077	snp	A/C	1.65318e-05	0.002875	missense	DTX2	GRCh38.p7	7:76505432	TCACAGTGGGCACGT[A/C]CAGCACCACGGGTGA	113878
rs761244074	snp	A/G	0.000104723	0.00723537	synonymous-codon	DTX2	GRCh38.p7	7:76500451	TCTAGGAGCGACCCC[A/G]AAGCCAGAGCCAGAG	113878
rs761244579	snp	C/G	1.65468e-05	0.00287631	intron-variant	DTX2	GRCh38.p7	7:76503611	CCTTCTTGAGTCCCC[C/G]ACTCCTGGCCACTCC	113878
rs761375152	in-del	-/AGCCAG	0.00165309	0.0287021	cds-indel	DTX2	GRCh38.p7	7:76500452	TAGGAGCGACCCCGA[-/AGCCAG]AGCCAGAGCCAGAGC	113878
rs761434032	snp	C/T	1.67435e-05	0.00289335	missense, intron-variant	DTX2	GRCh38.p7	7:76503555	GACTGCGGGACCATC[C/T]TCATAGTTTACAGCA	113878
rs761443424	snp	C/T	1.77615e-05	0.00298001	synonymous-codon, intron-variant	DTX2	GRCh38.p7	7:76497456	GGCTCAGTTAAGAGA[C/T]TGAGGAAAATGTCCG	113878
rs761554477	snp	C/T	1.80902e-05	0.00300745	intron-variant	DTX2	GRCh38.p7	7:76482462	GAACGTTCCCTGTAT[C/T]TTGGGGATGCTAGCA	113878
rs761570621	snp	A/G	0.00113035	0.0237465	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502473	TGCCCCCACTGGCCC[A/G]GGGCGGAGGCGGGTG	113878
rs761652752	snp	C/T	9.03526e-05	0.00672072	utr-variant-5-prime, upstream-variant-2KB	DTX2	GRCh38.p7	7:76480493	TGTTTGGGAAAGCAG[C/T]GGGACTCCTTGGGAA	113878
rs761665777	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76491196	AGAGACAGGATTTTG[C/T]CATCTTGGCCAGGCT	113878
rs761778612	snp	C/T	3.30442e-05	0.0040646	synonymous-codon	DTX2	GRCh38.p7	7:76482863	TGGCAGCAGAACTGG[C/T]CCCGTGTCAGGCCGC	113878
rs761833509	snp	G/T	0.00025826	0.0113606	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505699	CCGAGAGGCTGGGAG[G/T]TTTGTTGAGGGTGTG	113878
rs761907061	snp	C/T	1.66588e-05	0.00288602	synonymous-codon	DTX2	GRCh38.p7	7:76482695	CCTGGGGTACAACTA[C/T]ACTGTCAACTACACC	113878
rs762387798	snp	A/G	2.10378e-05	0.00324322	utr-variant-5-prime, upstream-variant-2KB	DTX2	GRCh38.p7	7:76480505	CAGCGGGACTCCTTG[A/G]GAAGATGGCCATGGC	113878
rs762406130	snp	C/T	5.32042e-05	0.00515745	intron-variant	DTX2	GRCh38.p7	7:76500390	TCGCCCTCTGGCCTC[C/T]TCTCCAGCCTGTGCT	113878
rs762466989	snp	C/T	3.29701e-05	0.00406005	missense	DTX2	GRCh38.p7	7:76482918	CCTGCATACCCCGTC[C/T]CCCAGCACCCCCCAC	113878
rs762712606	snp	C/T	2.51228e-05	0.00354412	synonymous-codon	DTX2	GRCh38.p7	7:76492249	AGTCCAGCAGGCGCT[C/T]GCAGGTAGGTGCCTG	113878
rs762826288	snp	A/G			intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76476772	GGTATCAAAGGTGGC[A/G]GGCTTGGTGTGAGTA	113878
rs762849001	snp	A/T			intron-variant	DTX2	GRCh38.p7	7:76481825	TTTAGTTTTATTTTT[A/T]AAAGTATGGGTTTTT	113878
rs762947547	snp	C/G	5.15167e-05	0.00507501	synonymous-codon	DTX2	GRCh38.p7	7:76480572	CGCGGCTGTGGCCGT[C/G]TGGGAATGGCAGGAC	113878
rs762950989	snp	G/T	0.00142959	0.0266974	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505618	CTCGCACCCCAGCAC[G/T]CCCGCCTCTGGTGGC	113878
rs762997466	snp	C/T	0.000117569	0.0076662	missense, downstream-variant-500B	DTX2	GRCh38.p7	7:76502373	AGCAAGGCAATCGGG[C/T]CCCTAGCTGTGGGCC	113878
rs763169322	snp	A/T	1.67455e-05	0.00289352	missense, intron-variant	DTX2	GRCh38.p7	7:76503562	GGACCATCCTCATAG[A/T]TTACAGCATTCCCCA	113878
rs763364309	snp	A/G	3.61415e-05	0.00425082	intron-variant	DTX2	GRCh38.p7	7:76482471	CTGTATCTTGGGGAT[A/G]CTAGCAGACTAACCT	113878
rs763742769	snp	C/T	3.32729e-05	0.00407864	missense	DTX2	GRCh38.p7	7:76482718	ACTACACCACCCACA[C/T]GCAGACCAACAAGAC	113878
rs763824482	snp	A/C/G	3.34942e-05	0.00409221	missense, intron-variant	DTX2	GRCh38.p7	7:76503511	AGATGGAGGTATTAC[A/C/G]GTTCCAGATGTCGCT	113878
rs763999026	snp	A/C/G	2.66571e-05	0.00365073	missense	DTX2	GRCh38.p7	7:76505545	AACTACCTGCAGAAC[A/C/G]TGCTGGCTGAGCTGG	113878
rs764137584	snp	A/G			intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76479734	AGGTTGCAGTGAGCC[A/G]AGATCACACGCCTGG	113878
rs764145554	snp	A/G	3.30617e-05	0.00406568	missense	DTX2	GRCh38.p7	7:76482618	ACTGCCTATGAAGCC[A/G]GCGTCTGTGACTATC	113878
rs764156140	snp	A/G	0.00867874	0.0652997	synonymous-codon	DTX2	GRCh38.p7	7:76482782	AGGGCCGCCTTACCC[A/G]GTGACCACCATCATC	113878
rs764238019	snp	C/T	3.43708e-05	0.00414538	intron-variant	DTX2	GRCh38.p7	7:76505346	CTCCGTCCCCTCCTT[C/T]CTCTTCCCCCTCCTC	113878
rs764329477	snp	C/G	1.67253e-05	0.00289178	missense	DTX2	GRCh38.p7	7:76482543	AGACACCTGTTCCCC[C/G]AGCACTCAGCCCCTG	113878
rs764351511	snp	C/T	0.000132135	0.00812713	missense	DTX2	GRCh38.p7	7:76482976	ACCAGGCCTTTGCAC[C/T]GTACAACAAACCCTC	113878
rs764404421	snp	A/C/G	3.43131e-05	0.00414193	synonymous-codon	DTX2	GRCh38.p7	7:76480686	TGGGCTTGGGAGCCT[A/C/G]GCCCACAGCATCCCC	113878
rs764457239	snp	C/T			intron-variant, upstream-variant-2KB, utr-variant-5-prime	DTX2	GRCh38.p7	7:76479104	AGCCACACGTGGACG[C/T]GGTTACTAGGGTTCT	113878
rs764509375	snp	A/G			synonymous-codon, intron-variant	DTX2	GRCh38.p7	7:76503473	CATCTATGGAGAGAA[A/G]ACGGGGACCCAGCCC	113878
rs764614517	snp	C/T	3.75002e-05	0.00432998	synonymous-codon	DTX2	GRCh38.p7	7:76505433	CACAGTGGGCACGTC[C/T]AGCACCACGGGTGAG	113878
rs764648661	snp	A/C			missense	DTX2	GRCh38.p7	7:76500452	CTAGGAGCGACCCCG[A/C]AGCCAGAGCCAGAGC	113878
rs764703677	snp	C/G	1.69983e-05	0.00291528	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502259	CACGTCAGCCCAGCC[C/G]ACTGTTGGCGAGCAT	113878
rs764704468	snp	C/T	1.65192e-05	0.00287391	missense	DTX2	GRCh38.p7	7:76482864	GGCAGCAGAACTGGC[C/T]CCGTGTCAGGCCGCT	113878
rs764721404	snp	G/T	1.77839e-05	0.00298189	missense, intron-variant	DTX2	GRCh38.p7	7:76497457	GCTCAGTTAAGAGAT[G/T]GAGGAAAATGTCCGT	113878
rs764883046	snp	A/G	0.00016758	0.00915215	missense, intron-variant	DTX2	GRCh38.p7	7:76497390	GTGTGTCTTAGCCGC[A/G]CACCCCAGCCCACCA	113878
rs765101680	snp	A/G	1.68513e-05	0.00290265	missense, downstream-variant-500B	DTX2	GRCh38.p7	7:76502382	ATCGGGTCCCTAGCT[A/G]TGGGCCACCTCACCA	113878
rs765119620	snp	A/G	1.65386e-05	0.00287559	utr-variant-5-prime, upstream-variant-2KB	DTX2	GRCh38.p7	7:76480494	GTTTGGGAAAGCAGC[A/G]GGACTCCTTGGGAAG	113878
rs765227179	snp	G/T	0.000601142	0.0173266	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505700	CGAGAGGCTGGGAGG[G/T]TTGTTGAGGGTGTGG	113878
rs765387474	snp	C/G			intron-variant	DTX2	GRCh38.p7	7:76505320	TGCCTGCTCACTGAG[C/G]CCCTCTCACTCTCCG	113878
rs765433775	snp	A/G	6.87994e-05	0.00586472	synonymous-codon	DTX2	GRCh38.p7	7:76505442	CACGTCCAGCACCAC[A/G]GGTGAGACGGACACC	113878
rs765492234	snp	A/G			intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76501990	CCCCTGAGTTCAAGC[A/G]ATTCTCTTGCCTCAG	113878
rs765567732	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76488056	TGGATCCTTGTACGG[C/T]TCAGTTCCTAGAGGT	113878
rs765638612	in-del	-/G			intron-variant	DTX2	GRCh38.p7	7:76498809	GGTGTGTGGAGGTGT[-/G]GGGGTGTGTGGGGTG	113878
rs765664461	in-del	-/CCC			intron-variant	DTX2	GRCh38.p7	7:76468439	CTCAGCCAAATCTGG[-/CCC]ACTGCCATTTTTTTT	113878
rs765684567	snp	C/T	0.000574941	0.0169452	synonymous-codon	DTX2	GRCh38.p7	7:76480776	GTTCCGCCAGGACAC[C/T]GGTAAGACGCTGTCT	113878
rs765845899	snp	C/T	1.72329e-05	0.00293533	synonymous-codon	DTX2	GRCh38.p7	7:76480695	GAGCCTGGCCCACAG[C/T]ATCCCCTTGGGCCAG	113878
rs765845959	snp	C/T	5.01341e-05	0.00500645	synonymous-codon	DTX2	GRCh38.p7	7:76483034	GCTGAACACCACCAA[C/T]GCCTGGGGCGCAGCT	113878
rs765850925	snp	A/G	5.15282e-05	0.00507558	stop-gained	DTX2	GRCh38.p7	7:76480574	CGGCTGTGGCCGTGT[A/G]GGAATGGCAGGACGG	113878
rs765851932	in-del	-/G	0.00118064	0.0242678	intron-variant	DTX2	GRCh38.p7	7:76504466	TGCCACCATGCGCCC[-/G]GGGGGTGGACGGGGC	113878
rs765864484	snp	A/C	6.5937e-05	0.00574144	missense	DTX2	GRCh38.p7	7:76482921	GCATACCCCGTCCCC[A/C]AGCACCCCCCACACA	113878
rs765900261	in-del	-/T	1.82068e-05	0.00301713	intron-variant	DTX2	GRCh38.p7	7:76503411	GCTCAGTGGGTTGCG[-/T]TCTGCCTCTGTCAGG	113878
rs765903594	snp	A/G	5.73455e-05	0.00535439	missense	DTX2	GRCh38.p7	7:76480525	ATGGCCATGGCCCCA[A/G]GCCCTTCCCTGGTGC	113878
rs765960793	in-del	-/A			intron-variant	DTX2	GRCh38.p7	7:76466986	GATCACTGCCGCCCC[-/A]AATTCCTGGGTTCAA	113878
rs765964433	snp	A/G	1.91896e-05	0.00309749	intron-variant	DTX2	GRCh38.p7	7:76497487	TGAAAGGTAGTTCTT[A/G]TTCCCAAAAGCTCTC	113878
rs766027737	snp	A/T	1.65113e-05	0.00287322	missense	DTX2	GRCh38.p7	7:76482870	AGAACTGGCCCCGTG[A/T]CAGGCCGCTACCGCC	113878
rs766115071	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76464699	ACCGTGCCTGGCCTC[A/G]TGAGGGACATTTTAA	113878
rs766189525	snp	A/G	3.26036e-05	0.00403741	missense	DTX2	GRCh38.p7	7:76492253	CAGCAGGCGCTCGCA[A/G]GTAGGTGCCTGACCT	113878
rs766243282	snp	G/T	4.48914e-05	0.00473747	intron-variant	DTX2	GRCh38.p7	7:76492121	CCAATAAGTCAGCGG[G/T]GTGCAGTAAGCTCTG	113878
rs766248708	snp	C/G/T	0.000181942	0.00953634	missense	DTX2	GRCh38.p7	7:76482630	GCCAGCGTCTGTGAC[C/G/T]ATCTGGAGCAGCAGG	113878
rs766376964	snp	A/G	3.612e-05	0.00424955	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502481	CTGGCCCAGGGCGGA[A/G]GCGGGTGGCCCGCCC	113878
rs766396204	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76501090	ACTGAGCCACGTTTT[A/G]GGGGCTGCAGCACCA	113878
rs766432007	snp	A/G	0.000337939	0.0129944	intron-variant	DTX2	GRCh38.p7	7:76503396	TGTTCTCAGACTGCC[A/G]GCTCAGTGGGTTGCG	113878
rs766439166	snp	C/T	1.67947e-05	0.00289777	missense, downstream-variant-500B	DTX2	GRCh38.p7	7:76502374	GCAAGGCAATCGGGT[C/T]CCTAGCTGTGGGCCA	113878
rs766544115	snp	C/T	0.00010227	0.00715016	synonymous-codon	DTX2	GRCh38.p7	7:76505526	CCACGGCTATCCCGA[C/T]CCCAACTACCTGCAG	113878
rs766617296	snp	C/T	2.38718e-05	0.00345475	intron-variant	DTX2	GRCh38.p7	7:76480784	AGGACACCGGTAAGA[C/T]GCTGTCTGCCTCTCG	113878
rs766618118	snp	C/T	5.43188e-05	0.00521118	intron-variant	DTX2	GRCh38.p7	7:76503627	ACTCCTGGCCACTCC[C/T]CTTCCCACCCCGCCC	113878
rs766697228	snp	C/T	1.69519e-05	0.0029113	synonymous-codon, intron-variant	DTX2	GRCh38.p7	7:76497404	CGCACCCCAGCCCAC[C/T]AGCCCTCCCGCCTCC	113878
rs766735237	in-del	-/AA	1.69772e-05	0.00291347	frameshift-variant	DTX2	GRCh38.p7	7:76480663	TCCAGCAGAAGGGCC[-/AA]AACGTTTTGGGCTTG	113878
rs766952685	snp	G/T	3.4071e-05	0.00412727	missense	DTX2	GRCh38.p7	7:76480671	GAAGGGCCAACGTTT[G/T]GGGCTTGGGAGCCTG	113878
rs766966279	snp	C/T	1.67753e-05	0.00289609	missense, intron-variant	DTX2	GRCh38.p7	7:76503576	GTTTACAGCATTCCC[C/T]ATGGTATCCAGGTGA	113878
rs767019386	snp	C/G	1.85589e-05	0.00304616	intron-variant	DTX2	GRCh38.p7	7:76503402	CAGACTGCCAGCTCA[C/G]TGGGTTGCGTCTGCC	113878
rs767077825	in-del	-/A			intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76475703	AAATAAAAAAAAAGA[-/A]AAAAAATCCCATAAT	113878
rs767227824	snp	A/G	1.6504e-05	0.00287258	missense	DTX2	GRCh38.p7	7:76482964	TGTTTGGGACCCACC[A/G]GGCCTTTGCACCGTA	113878
rs767311932	snp	A/G	1.67671e-05	0.00289539	missense, intron-variant	DTX2	GRCh38.p7	7:76503490	CGGGGACCCAGCCCC[A/G]GGGAAAGATGGAGGT	113878
rs767412406	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76498425	AGACTCGTTGGCAGC[C/T]CGGGCTGGCAACCTT	113878
rs767477706	snp	A/G	3.59913e-05	0.00424197	intron-variant	DTX2	GRCh38.p7	7:76482482	GGATGCTAGCAGACT[A/G]ACCTTTTGTTTTCCT	113878
rs767509314	snp	C/T	6.8327e-05	0.00584456	intron-variant	DTX2	GRCh38.p7	7:76492276	CCTGACCTCGGGCTG[C/T]AGAGCAGTCTGTGCC	113878
rs767569894	snp	C/T	1.85754e-05	0.00304752	intron-variant	DTX2	GRCh38.p7	7:76483195	CCCTGTGTTTCCGCT[C/T]TTAGCCGGGAAGACT	113878
rs767675268	snp	C/T	1.68363e-05	0.00290136	missense	DTX2	GRCh38.p7	7:76482531	CGGGCTGTGCGGAGA[C/T]ACCTGTTCCCCCAGC	113878
rs767727619	snp	A/G	3.53513e-05	0.00420409	missense	DTX2	GRCh38.p7	7:76483137	GGATCCTCCACCTCC[A/G]GTGCAGTCAGGTATC	113878
rs767772081	snp	C/T	5.30969e-05	0.00515224	intron-variant	DTX2	GRCh38.p7	7:76500420	TCCTCAGGACGCTGC[C/T]TATGTACTTCTCTCT	113878
rs767995188	snp	C/T	1.66222e-05	0.00288285	intron-variant	DTX2	GRCh38.p7	7:76480827	TGCCGCACCTGCTTT[C/T]CCACAGGCTCTGCGC	113878
rs768094479	snp	A/G	6.53944e-05	0.00571777	intron-variant	DTX2	GRCh38.p7	7:76503639	TCCTCTTCCCACCCC[A/G]CCCACATCCCAGCAG	113878
rs768155478	snp	C/T	1.7582e-05	0.00296491	intron-variant	DTX2	GRCh38.p7	7:76505334	GCCCCTCTCACTCTC[C/T]GTCCCCTCCTTCCTC	113878
rs768279091	snp	A/G	1.75443e-05	0.00296173	missense	DTX2	GRCh38.p7	7:76482510	CCTTTGAAAATAGGC[A/G]CCATGCGGGCTGTGC	113878
rs768322395	snp	G/T	0.000110193	0.00742188	intron-variant	DTX2	GRCh38.p7	7:76500348	TCGCATTTCCTCCTG[G/T]CAGCTTAGACCTCTT	113878
rs768405188	snp	A/C			intron-variant	DTX2	GRCh38.p7	7:76483414	CTCCACATGGAGCAG[A/C]GTTAAAGGCCTGTGG	113878
rs768456000	snp	A/G	1.73414e-05	0.00294455	missense	DTX2	GRCh38.p7	7:76483096	GCTCCAGCCTCTCCC[A/G]CCTGGGACCGCAGCA	113878
rs768512774	snp	C/G	1.65302e-05	0.00287486	missense	DTX2	GRCh38.p7	7:76482853	AGTGCCTCAGTGGCA[C/G]CAGAACTGGCCCCGT	113878
rs768583102	snp	A/C	0.0121947	0.0771273	intron-variant	DTX2	GRCh38.p7	7:76504461	GTGAGTGCCACCATG[A/C]GCCCGGGGGGTGGAC	113878
rs768588909	in-del	-/GGTTCCTCACTA	0.000348857	0.0132025	intron-variant	DTX2	GRCh38.p7	7:76500126	AGAAGCGCCGGGGTC[-/GGTTCCTCACTA]GGTTCCTCACTCAAT	113878
rs768671215	snp	C/T	3.5025e-05	0.00418465	missense, intron-variant	DTX2	GRCh38.p7	7:76497444	TCCAAAAGTCACGGC[C/T]CAGTTAAGAGATTGA	113878
rs768764013	snp	C/T	3.27338e-05	0.00404547	missense	DTX2	GRCh38.p7	7:76492245	GCAGAGTCCAGCAGG[C/T]GCTCGCAGGTAGGTG	113878
rs768767133	snp	A/G	1.65037e-05	0.00287256	intron-variant	DTX2	GRCh38.p7	7:76497311	TGTCTCTCCCTCTCT[A/G]CGTGTCTGCTCTCAC	113878
rs768926968	snp	A/G	1.68261e-05	0.00290048	missense, intron-variant	DTX2	GRCh38.p7	7:76503469	AAACCATCTATGGAG[A/G]GAAGACGGGGACCCA	113878
rs768952838	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76481060	GGCCGGCAGGCCGGC[A/G]TGGAGGTGGTGCGTC	113878
rs769059523	snp	C/G/T	0.000148181	0.00860631	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505605	GAGCAGCAGTGACCT[C/G/T]GCACCCCAGCACGCC	113878
rs769130113	snp	G/T	1.65143e-05	0.00287348	missense, downstream-variant-500B	DTX2	GRCh38.p7	7:76502315	CTGCATCATCTGCAT[G/T]GAGAAGCTGTCCACA	113878
rs769177459	snp	C/T	1.65457e-05	0.00287621	missense	DTX2	GRCh38.p7	7:76482756	TTCTGCCGCAGCGTG[C/T]GGCGCCAAGCAGGGC	113878
rs769220579	in-del	-/G			intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76472346	TTTGTTTTTTGTTTT[-/G]TTTTTTGAGGCTCAT	113878
rs769341153	snp	A/G	0.0001569	0.0088558	intron-variant	DTX2	GRCh38.p7	7:76500377	TTCCTTCCCTTCCTC[A/G]CCCTCTGGCCTCCTC	113878
rs769359297	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76483232	AATTCCTGCAGATGC[A/G]GCTCCTGCCCCCTAG	113878
rs769421747	snp	C/T	1.6495e-05	0.0028718	missense	DTX2	GRCh38.p7	7:76482943	CCCCACACAGGACCG[C/T]TTCTGTGTTTGGGAC	113878
rs769547551	snp	A/G	0.000168808	0.00918561	synonymous-codon	DTX2	GRCh38.p7	7:76480638	CTGCAGCTTCATCGA[A/G]CAGCAGTTTGTCCAG	113878
rs769574745	snp	C/T	1.72546e-05	0.00293718	synonymous-codon	DTX2	GRCh38.p7	7:76480569	CCCCGCGGCTGTGGC[C/T]GTGTGGGAATGGCAG	113878
rs769594727	snp	A/G	1.73661e-05	0.00294665	missense	DTX2	GRCh38.p7	7:76482515	GAAAATAGGCACCAT[A/G]CGGGCTGTGCGGAGA	113878
rs769623442	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76481476	ACAAGCATGAGCCAC[C/T]GCGCCTGGACCTGCA	113878
rs769680630	snp	A/G			utr-variant-3-prime	DTX2	GRCh38.p7	7:76505884	GGGCCCGCGGTGCTC[A/G]GGGCCTGGTGTGGGG	113878
rs769683109	in-del	-/TG			intron-variant	DTX2	GRCh38.p7	7:76482043	AGAGTCTGTGAAAAC[-/TG]TGGCTGTCAGTCAGC	113878
rs769752444	snp	G/T	0.000166681	0.00912757	intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501318	GTTTGGAAAGGAGCC[G/T]GAACGTCCTCCTCAT	113878
rs769827782	snp	C/G	1.65411e-05	0.00287581	missense	DTX2	GRCh38.p7	7:76482808	TCATCGCTCCGCCGG[C/G]CCACACAGGCGTCGC	113878
rs769857912	snp	A/G	3.30792e-05	0.00406675	synonymous-codon	DTX2	GRCh38.p7	7:76482764	CAGCGTGCGGCGCCA[A/G]GCAGGGCCGCCTTAC	113878
rs769884635	snp	C/T	2.55869e-05	0.0035767	synonymous-codon	DTX2	GRCh38.p7	7:76505517	CATTACGGGCCACGG[C/T]TATCCCGACCCCAAC	113878
rs770221413	in-del	-/C			intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76472076	CCTTTTCAAGCAAAG[-/C]CCCATCTCGCCGTGC	113878
rs770273048	snp	C/T	3.50349e-05	0.00418524	missense	DTX2	GRCh38.p7	7:76483116	GGACCGCAGCACCTG[C/T]CCCCAGGATCCTCCA	113878
rs770326343	snp	C/T	3.57609e-05	0.00422838	intron-variant	DTX2	GRCh38.p7	7:76483169	TGGGCAACGGCCGCT[C/T]GTTTTGTCTGCCCTG	113878
rs770326426	snp	A/T	1.80847e-05	0.00300699	intron-variant	DTX2	GRCh38.p7	7:76482464	ACGTTCCCTGTATCT[A/T]GGGGATGCTAGCAGA	113878
rs770491166	snp	A/C	4.37665e-05	0.00467775	synonymous-codon	DTX2	GRCh38.p7	7:76505421	GCGGCTCATCTTCAC[A/C]GTGGGCACGTCCAGC	113878
rs770572041	snp	C/T	0.000234256	0.01082	intron-variant	DTX2	GRCh38.p7	7:76500399	GGCCTCCTCTCCAGC[C/T]TGTGCTCCTCAGGAC	113878
rs770641812	snp	C/T	1.76092e-05	0.0029672	missense	DTX2	GRCh38.p7	7:76480727	CAGACCCCTCGCTGG[C/T]CCCTTACATTATTGA	113878
rs770677116	snp	A/G	1.64988e-05	0.00287213	intron-variant	DTX2	GRCh38.p7	7:76497315	TCTCCCTCTCTGCGT[A/G]TCTGCTCTCACACCC	113878
rs770841504	snp	A/G	3.36044e-05	0.00409891	synonymous-codon, intron-variant	DTX2	GRCh38.p7	7:76503476	CTATGGAGAGAAGAC[A/G]GGGACCCAGCCCCAG	113878
rs770973374	snp	A/C	1.76424e-05	0.00297	synonymous-codon	DTX2	GRCh38.p7	7:76480551	GGTGCAGGTGTACAC[A/C]AGCCCCGCGGCTGTG	113878
rs770997221	snp	C/T	0.0012747	0.0252136	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505874	GGGCTGCTTCGGGCC[C/T]GCGGTGCTCGGGGCC	113878
rs771152679	snp	A/G	0.000307267	0.0123911	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505622	CACCCCAGCACGCCC[A/G]CCTCTGGTGGCCACC	113878
rs771297466	snp	A/G	1.65384e-05	0.00287557	missense	DTX2	GRCh38.p7	7:76482822	GGCCACACAGGCGTC[A/G]CCTGCTCTTGCCACC	113878
rs771341183	snp	A/C			intron-variant	DTX2	GRCh38.p7	7:76500273	CGACGGAGCTCGGGG[A/C]TCTGTGCCTGGCGCT	113878
rs771569668	in-del	-/G	1.68001e-05	0.00289823	frameshift-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502315	CTGCATCATCTGCAT[-/G]GAGAAGCTGTCCACA	113878
rs771637071	snp	C/T	5.42098e-05	0.00520596	synonymous-codon	DTX2	GRCh38.p7	7:76480740	GGCCCCTTACATTAT[C/T]GACCTCCCCAGCTGG	113878
rs771655815	snp	A/T	1.68136e-05	0.0028994	missense, downstream-variant-500B	DTX2	GRCh38.p7	7:76502305	TCCTCCAGGACTGCA[A/T]CATCTGCATGGAGAA	113878
rs771754261	snp	G/T	6.85906e-05	0.00585582	intron-variant	DTX2	GRCh38.p7	7:76503594	GGTATCCAGGTGAGG[G/T]GCCTTCTTGAGTCCC	113878
rs771972559	snp	C/T	9.18709e-05	0.00677695	intron-variant	DTX2	GRCh38.p7	7:76480815	CACATATCTGGGTGC[C/T]GCACCTGCTTTCCCA	113878
rs771982305	snp	C/G	1.65658e-05	0.00287795	missense, intron-variant	DTX2	GRCh38.p7	7:76497373	CAGCCATTGGACTCC[C/G]TGTGTGTCTTAGCCG	113878
rs771985167	in-del	-/GT			intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76478684	CCCTAAACACTGGCA[-/GT]TTGCAGGTGTGAGCC	113878
rs772031003	snp	A/G/T	3.30749e-05	0.00406652	synonymous-codon	DTX2	GRCh38.p7	7:76482773	GCGCCAAGCAGGGCC[A/G/T]CCTTACCCGGTGACC	113878
rs772055212	snp	A/G	1.67424e-05	0.00289326	missense, intron-variant	DTX2	GRCh38.p7	7:76503544	CCGGCCACGAGGACT[A/G]CGGGACCATCCTCAT	113878
rs772180849	snp	C/T	3.32176e-05	0.00407526	synonymous-codon	DTX2	GRCh38.p7	7:76492228	GCAGATGCCAAAGCC[C/T]AGCAGAGTCCAGCAG	113878
rs772212863	snp	C/T	1.6863e-05	0.00290365	synonymous-codon	DTX2	GRCh38.p7	7:76480623	CTACAGTGCCACCGT[C/T]TGCAGCTTCATCGAG	113878
rs772220149	in-del	-/TA			upstream-variant-2KB	DTX2	GRCh38.p7	7:76460355	TATTATTATTATTAT[-/TA]TTTTTTTTTTTTTTG	113878
rs772386339	snp	G/T			intron-variant, utr-variant-5-prime, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76470415	GGGTCCCCAGAGAAG[G/T]CAAGGTAATCATCCT	113878
rs772447293	snp	A/G	3.49229e-05	0.00417854	missense	DTX2	GRCh38.p7	7:76480558	GTGTACACCAGCCCC[A/G]CGGCTGTGGCCGTGT	113878
rs772539201	snp	C/T	1.70206e-05	0.00291719	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502252	ACTGGCCCACGTCAG[C/T]CCAGCCCACTGTTGG	113878
rs772565087	snp	C/T	4.104e-05	0.00452971	synonymous-codon	DTX2	GRCh38.p7	7:76505427	CATCTTCACAGTGGG[C/T]ACGTCCAGCACCACG	113878
rs772590571	snp	A/G	1.65252e-05	0.00287443	intron-variant	DTX2	GRCh38.p7	7:76497297	AAGGAGTCTTCTAAT[A/G]TCTCTCCCTCTCTGC	113878
rs772608727	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76481176	TGCTTTTTGGTCTGC[A/G]ATGTGTTTTGATCTT	113878
rs772614157	snp	A/G	7.87329e-05	0.00627378	missense	DTX2	GRCh38.p7	7:76505498	AGACAGAGATGGACC[A/G]CAACATTACGGGCCA	113878
rs772729416	snp	C/T	0.000154297	0.00878207	intron-variant	DTX2	GRCh38.p7	7:76500381	TTCCCTTCCTCGCCC[C/T]CTGGCCTCCTCTCCA	113878
rs772781142	in-del	-/AGA	1.68022e-05	0.00289842	cds-indel, downstream-variant-500B	DTX2	GRCh38.p7	7:76502317	GCATCATCTGCATGG[-/AGA]AGCTGTCCACAGCGT	113878
rs772890960	snp	C/T	7.33286e-05	0.00605466	synonymous-codon, intron-variant	DTX2	GRCh38.p7	7:76497470	ATTGAGGAAAATGTC[C/T]GTGAAAGGTAGTTCT	113878
rs772962215	snp	C/T	1.73555e-05	0.00294575	missense	DTX2	GRCh38.p7	7:76482516	AAAATAGGCACCATG[C/T]GGGCTGTGCGGAGAC	113878
rs773030862	snp	C/G	0.000168813	0.00918576	missense	DTX2	GRCh38.p7	7:76480639	TGCAGCTTCATCGAG[C/G]AGCAGTTTGTCCAGC	113878
rs773085420	snp	A/G	0.000103348	0.00718774	missense	DTX2	GRCh38.p7	7:76480570	CCCGCGGCTGTGGCC[A/G]TGTGGGAATGGCAGG	113878
rs773088098	snp	A/C/T	0.000113558	0.00753441	intron-variant	DTX2	GRCh38.p7	7:76503394	GGTGTTCTCAGACTG[A/C/T]CAGCTCAGTGGGTTG	113878
rs773143032	in-del	-/G			intron-variant	DTX2	GRCh38.p7	7:76491433	GCTGGGACTACAGCT[-/G]TGTGCCAGCATGCCC	113878
rs773145330	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76498427	ACTCGTTGGCAGCCC[A/G]GGCTGGCAACCTTCT	113878
rs773194901	snp	G/T	3.29891e-05	0.00406122	synonymous-codon	DTX2	GRCh38.p7	7:76482944	CCCACACAGGACCGC[G/T]TCTGTGTTTGGGACC	113878
rs773195533	snp	A/G	1.67388e-05	0.00289294	missense, downstream-variant-500B	DTX2	GRCh38.p7	7:76502331	GAGAAGCTGTCCACA[A/G]CGTCTGGATACAGCG	113878
rs773361567	snp	A/G	1.65389e-05	0.00287562	missense	DTX2	GRCh38.p7	7:76482769	TGCGGCGCCAAGCAG[A/G]GCCGCCTTACCCGGT	113878
rs773421398	snp	A/G	1.6659e-05	0.00288604	missense	DTX2	GRCh38.p7	7:76482699	GGGTACAACTACACT[A/G]TCAACTACACCACCC	113878
rs773471312	snp	A/C	2.5583e-05	0.00357643	missense	DTX2	GRCh38.p7	7:76505522	CGGGCCACGGCTATC[A/C]CGACCCCAACTACCT	113878
rs773506200	snp	A/G	1.65685e-05	0.00287819	synonymous-codon, intron-variant	DTX2	GRCh38.p7	7:76497368	GATGTCAGCCATTGG[A/G]CTCCCTGTGTGTCTT	113878
rs773707841	snp	G/T	1.68055e-05	0.0028987	missense, downstream-variant-500B	DTX2	GRCh38.p7	7:76502371	ACAGCAAGGCAATCG[G/T]GTCCCTAGCTGTGGG	113878
rs773754831	in-del	-/T			intron-variant	DTX2	GRCh38.p7	7:76490995	GCTATGAGAACCTGC[-/T]TTTTTTTTTTTTTTT	113878
rs773824914	snp	C/G	1.65004e-05	0.00287227	missense	DTX2	GRCh38.p7	7:76482954	ACCGCTTCTGTGTTT[C/G]GGACCCACCAGGCCT	113878
rs773838700	snp	A/G	1.75468e-05	0.00296194	synonymous-codon	DTX2	GRCh38.p7	7:76483121	GCAGCACCTGCCCCC[A/G]GGATCCTCCACCTCC	113878
rs773999130	snp	G/T	4.31397e-05	0.00464414	missense	DTX2	GRCh38.p7	7:76505422	CGGCTCATCTTCACA[G/T]TGGGCACGTCCAGCA	113878
rs774058609	in-del	-/GAG			intron-variant	DTX2	GRCh38.p7	7:76483763	GGTGGCATTTAAAAT[-/GAG]GAGATTGGTCAGGCA	113878
rs774218815	in-del	-/C	0.000304275	0.0123307	intron-variant	DTX2	GRCh38.p7	7:76500309	CTCCCGTCCCGCACA[-/C]TGGCCTCCCTGTCTG	113878
rs774229088	snp	C/G	1.69663e-05	0.00291253	missense	DTX2	GRCh38.p7	7:76480661	TTGTCCAGCAGAAGG[C/G]CCAACGTTTTGGGCT	113878
rs774282054	snp	C/G	7.07752e-05	0.00594833	missense	DTX2	GRCh38.p7	7:76480730	ACCCCTCGCTGGCCC[C/G]TTACATTATTGACCT	113878
rs774305774	snp	C/T	1.64974e-05	0.00287201	intron-variant	DTX2	GRCh38.p7	7:76497320	CTCTCTGCGTGTCTG[C/T]TCTCACACCCGTGCA	113878
rs774312459	snp	A/C	1.76565e-05	0.00297118	missense	DTX2	GRCh38.p7	7:76483131	CCCCCAGGATCCTCC[A/C]CCTCCGGTGCAGTCA	113878
rs774413822	snp	A/G	1.87806e-05	0.0030643	intron-variant	DTX2	GRCh38.p7	7:76503397	GTTCTCAGACTGCCA[A/G]CTCAGTGGGTTGCGT	113878
rs774439426	snp	A/G	1.72484e-05	0.00293665	missense, downstream-variant-500B	DTX2	GRCh38.p7	7:76502448	GCCATGTACTGCAAC[A/G]GCAATAAGGTGCCCC	113878
rs774467274	snp	A/C	1.67778e-05	0.00289631	missense, intron-variant	DTX2	GRCh38.p7	7:76503486	AAGACGGGGACCCAG[A/C]CCCAGGGAAAGATGG	113878
rs774548053	snp	A/G	1.65184e-05	0.00287384	missense	DTX2	GRCh38.p7	7:76482594	TGGCTGAGCGACGAT[A/G]GCTCCTGGACTGCCT	113878
rs774600171	snp	C/G	0.00254777	0.0356004	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505892	GGTGCTCGGGGCCTG[C/G]TGTGGGGCGAGTAGA	113878
rs774600298	snp	C/G	1.67973e-05	0.00289799	missense, downstream-variant-500B	DTX2	GRCh38.p7	7:76502376	AAGGCAATCGGGTCC[C/G]TAGCTGTGGGCCACC	113878
rs774607429	snp	C/G	5.3126e-05	0.00515366	intron-variant	DTX2	GRCh38.p7	7:76505329	ACTGAGCCCCTCTCA[C/G]TCTCCGTCCCCTCCT	113878
rs774623322	in-del	-/TT/TTAT			upstream-variant-2KB	DTX2	GRCh38.p7	7:76460354	TTATTATTATTATTA[-/TT/TTAT]TTTTTTTTTTTTTTT	113878
rs774673597	snp	C/T	1.65326e-05	0.00287507	missense	DTX2	GRCh38.p7	7:76482825	CACACAGGCGTCGCC[C/T]GCTCTTGCCACCAGT	113878
rs774775418	snp	C/T	0.000179864	0.00948155	missense	DTX2	GRCh38.p7	7:76492194	GCAGCCCAGGGAGCG[C/T]CCCTGCCACTGTGCC	113878
rs774827421	in-del	-/TGTAGTGAAT			intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76472869	TAATAGAGACAGTGC[-/TGTAGTGAAT]AGCTTCACGTCAAAA	113878
rs774852183	snp	C/T	0.000129365	0.0080415	intron-variant	DTX2	GRCh38.p7	7:76483191	TCTGCCCTGTGTTTC[C/T]GCTCTTAGCCGGGAA	113878
rs775032249	snp	A/T	0.00011041	0.00742918	missense	DTX2	GRCh38.p7	7:76480745	CTTACATTATTGACC[A/T]CCCCAGCTGGACCCA	113878
rs775217433	snp	A/T	1.68083e-05	0.00289894	missense, downstream-variant-500B	DTX2	GRCh38.p7	7:76502308	TCCAGGACTGCATCA[A/T]CTGCATGGAGAAGCT	113878
rs775221494	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76481812	TTTCAATTTTAATTT[C/T]AGTTTTATTTTTAAA	113878
rs775237045	snp	C/T	0.000100526	0.00708893	synonymous-codon, intron-variant	DTX2	GRCh38.p7	7:76503545	CGGCCACGAGGACTG[C/T]GGGACCATCCTCATA	113878
rs775405620	snp	A/G	6.98434e-05	0.00590904	missense, intron-variant	DTX2	GRCh38.p7	7:76497441	GCTTCCAAAAGTCAC[A/G]GCTCAGTTAAGAGAT	113878
rs775526701	snp	A/G	4.85826e-05	0.00492838	synonymous-codon	DTX2	GRCh38.p7	7:76492240	GCCCAGCAGAGTCCA[A/G]CAGGCGCTCGCAGGT	113878
rs775584121	in-del	-/AT			intron-variant	DTX2	GRCh38.p7	7:76481619	ACAATGTTTGGAGAC[-/AT]TGTTGGTTGTTACAG	113878
rs775753992	snp	C/T	1.86548e-05	0.00305402	intron-variant	DTX2	GRCh38.p7	7:76483197	CTGTGTTTCCGCTCT[C/T]AGCCGGGAAGACTCA	113878
rs775816588	snp	C/T	5.23821e-05	0.00511745	missense	DTX2	GRCh38.p7	7:76480559	TGTACACCAGCCCCG[C/T]GGCTGTGGCCGTGTG	113878
rs775845256	in-del	-/T			upstream-variant-2KB	DTX2	GRCh38.p7	7:76460519	ACTACGCCCGCTTAA[-/T]TTTTTTTTTTTTTTG	113878
rs775933858	snp	C/T	1.65255e-05	0.00287445	missense	DTX2	GRCh38.p7	7:76482607	ATGGCTCCTGGACTG[C/T]CTATGAAGCCAGCGT	113878
rs776021087	snp	C/G/T	0.000935231	0.0216045	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502253	CTGGCCCACGTCAGC[C/G/T]CAGCCCACTGTTGGC	113878
rs776131330	snp	A/G	0.000108737	0.0073727	intron-variant	DTX2	GRCh38.p7	7:76505335	CCCCTCTCACTCTCC[A/G]TCCCCTCCTTCCTCT	113878
rs776142303	snp	C/T	1.73827e-05	0.00294806	intron-variant	DTX2	GRCh38.p7	7:76503609	GGCCTTCTTGAGTCC[C/T]CCACTCCTGGCCACT	113878
rs776306896	snp	C/T	1.67435e-05	0.00289335	synonymous-codon, intron-variant	DTX2	GRCh38.p7	7:76503554	GGACTGCGGGACCAT[C/T]CTCATAGTTTACAGC	113878
rs776334760	snp	A/G			utr-variant-3-prime	DTX2	GRCh38.p7	7:76505875	GGCTGCTTCGGGCCC[A/G]CGGTGCTCGGGGCCT	113878
rs776357746	snp	C/T	3.48292e-05	0.00417294	missense	DTX2	GRCh38.p7	7:76483105	TCTCCCACCTGGGAC[C/T]GCAGCACCTGCCCCC	113878
rs776365572	snp	C/G	1.77065e-05	0.00297539	missense, intron-variant	DTX2	GRCh38.p7	7:76497454	ACGGCTCAGTTAAGA[C/G]ATTGAGGAAAATGTC	113878
rs776403312	snp	C/G	3.64252e-05	0.00426747	intron-variant	DTX2	GRCh38.p7	7:76480829	CCGCACCTGCTTTCC[C/G]ACAGGCTCTGCGCCA	113878
rs776464727	snp	C/G	1.64846e-05	0.0028709	missense	DTX2	GRCh38.p7	7:76482912	AACCTCCCTGCATAC[C/G]CCGTCCCCCAGCACC	113878
rs776499453	snp	C/G	0.00011633	0.00762572	missense	DTX2	GRCh38.p7	7:76482854	GTGCCTCAGTGGCAG[C/G]AGAACTGGCCCCGTG	113878
rs776547636	snp	C/G	4.77909e-05	0.00488806	utr-variant-5-prime, upstream-variant-2KB	DTX2	GRCh38.p7	7:76480484	GTCTGAAGCTGTTTG[C/G]GAAAGCAGCGGGACT	113878
rs776671136	snp	A/G	1.66601e-05	0.00288614	synonymous-codon	DTX2	GRCh38.p7	7:76482683	GGACTTGGCCCCCCT[A/G]GGGTACAACTACACT	113878
rs776853130	snp	C/T	3.26557e-05	0.00404064	missense	DTX2	GRCh38.p7	7:76492248	GAGTCCAGCAGGCGC[C/T]CGCAGGTAGGTGCCT	113878
rs776952855	snp	C/G			intron-variant	DTX2	GRCh38.p7	7:76485049	GGAAGGCAGGGGGCT[C/G]TTTTAATACATTTTA	113878
rs777086054	in-del	-/C	3.46542e-05	0.00416244	intron-variant	DTX2	GRCh38.p7	7:76503606	GGGGCCTTCTTGAGT[-/C]CCCCCACTCCTGGCC	113878
rs777111226	snp	C/T			utr-variant-3-prime	DTX2	GRCh38.p7	7:76505769	CTCTCTCTCCTCCTC[C/T]CCTCTGGGAATTGGG	113878
rs777158978	snp	A/C/G	0.00452847	0.0473686	synonymous-codon	DTX2	GRCh38.p7	7:76483031	CAGGCTGAACACCAC[A/C/G]AACGCCTGGGGCGCA	113878
rs777293914	in-del	-/CAAAAAA			intron-variant	DTX2	GRCh38.p7	7:76463066	AGGGAGACCCCGTCT[-/CAAAAAA]CAAAAAACAAACAAA	113878
rs777307642	snp	A/G	0.000165254	0.00908843	intron-variant	DTX2	GRCh38.p7	7:76497286	GTCACATGCCGAAGG[A/G]GTCTTCTAATGTCTC	113878
rs777357419	snp	C/T			downstream-variant-500B	DTX2	GRCh38.p7	7:76506153	GCATGGAGGAGCCCA[C/T]GGTACTGGGCTGTGC	113878
rs777415062	snp	C/T	4.98583e-05	0.00499266	synonymous-codon	DTX2	GRCh38.p7	7:76482665	CAGGGGCAACCAGCT[C/T]GTGGACTTGGCCCCC	113878
rs777517183	snp	C/T	3.3145e-05	0.0040708	missense	DTX2	GRCh38.p7	7:76483005	TCACTCTCCGGGGCC[C/T]GGTCTGCGCCCAGGC	113878
rs777578252	snp	A/G	1.65266e-05	0.00287455	missense	DTX2	GRCh38.p7	7:76482588	TGGGAGTGGCTGAGC[A/G]ACGATGGCTCCTGGA	113878
rs777617264	snp	C/T	0.00016707	0.00913823	intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501322	GGAAAGGAGCCTGAA[C/T]GTCCTCCTCATGTGT	113878
rs777742013	snp	A/G	1.68522e-05	0.00290272	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502287	CATGACCCATGTTTG[A/G]TCTCCTCCAGGACTG	113878
rs777873988	snp	C/T	1.654e-05	0.00287571	synonymous-codon	DTX2	GRCh38.p7	7:76482818	GCCGGGCCACACAGG[C/T]GTCGCCTGCTCTTGC	113878
rs778077665	snp	A/G	3.41577e-05	0.00413251	intron-variant	DTX2	GRCh38.p7	7:76503590	CCATGGTATCCAGGT[A/G]AGGGGCCTTCTTGAG	113878
rs778090809	snp	A/G	1.64914e-05	0.00287149	missense	DTX2	GRCh38.p7	7:76482886	CAGGCCGCTACCGCC[A/G]CTCCATGACCAACCT	113878
rs778143954	snp	A/C	1.77084e-05	0.00297554	missense	DTX2	GRCh38.p7	7:76480549	CTGGTGCAGGTGTAC[A/C]CCAGCCCCGCGGCTG	113878
rs778181397	snp	C/T	7.503e-05	0.00612449	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502494	GAGGCGGGTGGCCCG[C/T]CCCCACAGTCCTGAG	113878
rs778185566	snp	G/T	1.70208e-05	0.00291721	missense	DTX2	GRCh38.p7	7:76480592	AATGGCAGGACGGGC[G/T]GGGCACCTGGCACCC	113878
rs778192630	snp	A/G	9.92408e-05	0.00704348	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505823	GGGGGCTTAGGATGC[A/G]GCTACCTCAGTGCGC	113878
rs778198302	in-del	-/A	0.000148494	0.00861539	frameshift-variant	DTX2	GRCh38.p7	7:76482932	CCCCCAGCACCCCCC[-/A]CACAGGACCGCTTCT	113878
rs778202426	snp	A/G	0.359655	0.224668	intron-variant	DTX2	GRCh38.p7	7:76504321	CCTGTGCGGGCTCTC[A/G]GAGCACCCTATCCTG	113878
rs778207414	snp	C/T	1.70781e-05	0.00292212	missense, downstream-variant-500B	DTX2	GRCh38.p7	7:76502434	TGCTGTGCCTCCTGG[C/T]CATGTACTGCAACGG	113878
rs778266867	snp	C/T	1.68337e-05	0.00290114	synonymous-codon, downstream-variant-500B	DTX2	GRCh38.p7	7:76502300	TGGTCTCCTCCAGGA[C/T]TGCATCATCTGCATG	113878
rs778434414	snp	C/T	9.9341e-05	0.00704703	missense	DTX2	GRCh38.p7	7:76482747	ACTTCCAGCTTCTGC[C/T]GCAGCGTGCGGCGCC	113878
rs778463778	snp	C/G	3.59253e-05	0.00423809	missense	DTX2	GRCh38.p7	7:76505576	CTGCCCAGGGGGTGA[C/G]CGAGGACTGCCTGGA	113878
rs778489108	snp	A/G	9.89952e-05	0.00703476	synonymous-codon, intron-variant	DTX2	GRCh38.p7	7:76497344	CCGTGCAGGCATGAC[A/G]AGTGTTCTGATGTCA	113878
rs778500050	snp	A/G	2.81472e-05	0.00375137	missense	DTX2	GRCh38.p7	7:76505470	ACCGTGGTATGGAAC[A/G]AGATCCACCACAAGA	113878
rs778577800	snp	A/G	1.66288e-05	0.00288343	synonymous-codon	DTX2	GRCh38.p7	7:76482674	CCAGCTCGTGGACTT[A/G]GCCCCCCTGGGGTAC	113878
rs778614789	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76503303	TCCGGGCAGGAGGCT[A/G]CCAGCAACTCCCTGG	113878
rs778806693	in-del	-/ATT			upstream-variant-2KB	DTX2	GRCh38.p7	7:76460335	CACCACACCCAGTTA[-/ATT]ATTATTATTATTATT	113878
rs778870566	snp	A/C/T	5.03388e-05	0.0050167	missense, downstream-variant-500B	DTX2	GRCh38.p7	7:76502353	GATACAGCGATGTGA[A/C/T]TGACAGCAAGGCAAT	113878
rs779129877	snp	C/G	1.75693e-05	0.00296384	missense	DTX2	GRCh38.p7	7:76480554	GCAGGTGTACACCAG[C/G]CCCGCGGCTGTGGCC	113878
rs779291726	snp	C/G	0.000115408	0.00759543	missense	DTX2	GRCh38.p7	7:76482895	ACCGCCACTCCATGA[C/G]CAACCTCCCTGCATA	113878
rs779329603	snp	C/T	1.92306e-05	0.00310079	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502496	GGCGGGTGGCCCGCC[C/T]CCACAGTCCTGAGCT	113878
rs779399752	snp	C/T	1.7246e-05	0.00293644	missense	DTX2	GRCh38.p7	7:76483084	AGCCCCTCTACCGCT[C/T]CAGCCTCTCCCACCT	113878
rs779455693	snp	C/G	1.73279e-05	0.00294341	missense, intron-variant	DTX2	GRCh38.p7	7:76503433	TCTGTCAGGATGGAA[C/G]TCTGCAGTGTCCCTC	113878
rs779458207	snp	A/G	2.56631e-05	0.00358202	missense	DTX2	GRCh38.p7	7:76505515	AACATTACGGGCCAC[A/G]GCTATCCCGACCCCA	113878
rs779523857	in-del	-/GCAGACCCCTC	6.9365e-05	0.00588877	frameshift-variant	DTX2	GRCh38.p7	7:76480711	ATCCCCTTGGGCCAG[-/GCAGACCCCTC]GCTGGCCCCTTACAT	113878
rs779688007	snp	C/T	0.0016767	0.0289057	synonymous-codon, downstream-variant-500B	DTX2	GRCh38.p7	7:76502408	CACCAAGTGCAGCCA[C/T]GCCTTCCACCTGCTG	113878
rs779805472	snp	A/G	6.27392e-05	0.00560051	intron-variant	DTX2	GRCh38.p7	7:76480816	ACATATCTGGGTGCC[A/G]CACCTGCTTTCCCAC	113878
rs779874454	in-del	-/CT	1.65155e-05	0.00287359	intron-variant	DTX2	GRCh38.p7	7:76497305	TTCTAATGTCTCTCC[-/CT]CTCTGCGTGTCTGCT	113878
rs779910965	snp	A/G	1.67882e-05	0.00289721	missense, downstream-variant-500B	DTX2	GRCh38.p7	7:76502359	GCGATGTGACTGACA[A/G]CAAGGCAATCGGGTC	113878
rs780106612	snp	C/G	1.719e-05	0.00293167	intron-variant	DTX2	GRCh38.p7	7:76503596	TATCCAGGTGAGGGG[C/G]CTTCTTGAGTCCCCC	113878
rs780204346	snp	A/G/T	5.05534e-05	0.00502738	missense, intron-variant	DTX2	GRCh38.p7	7:76503463	CCTGCAAAACCATCT[A/G/T]TGGAGAGAAGACGGG	113878
rs780237865	in-del	-/CCCA/CCT			downstream-variant-500B	DTX2	GRCh38.p7	7:76506050	TGTGTGTGTGTGTGC[-/CCCA/CCT]CCCCCCCCACTTCCT	113878
rs780280956	snp	C/G	1.72868e-05	0.00293992	synonymous-codon	DTX2	GRCh38.p7	7:76480701	GGCCCACAGCATCCC[C/G]TTGGGCCAGGCAGAC	113878
rs780357158	snp	A/G	5.02214e-05	0.00501081	synonymous-codon, intron-variant	DTX2	GRCh38.p7	7:76503524	ACGGTTCCAGATGTC[A/G]CTCCCCGGCCACGAG	113878
rs780368395	snp	C/T	3.30923e-05	0.00406756	synonymous-codon	DTX2	GRCh38.p7	7:76482752	CAGCTTCTGCCGCAG[C/T]GTGCGGCGCCAAGCA	113878
rs780438446	snp	A/T	1.68746e-05	0.00290466	missense	DTX2	GRCh38.p7	7:76480633	ACCGTCTGCAGCTTC[A/T]TCGAGCAGCAGTTTG	113878
rs780472737	snp	C/T	1.65239e-05	0.00287431	intron-variant	DTX2	GRCh38.p7	7:76497299	GGAGTCTTCTAATGT[C/T]TCTCCCTCTCTGCGT	113878
rs780539494	snp	C/T	1.74698e-05	0.00295544	synonymous-codon	DTX2	GRCh38.p7	7:76482512	TTTGAAAATAGGCAC[C/T]ATGCGGGCTGTGCGG	113878
rs780553587	snp	C/G			intron-variant	DTX2	GRCh38.p7	7:76498889	GTGTGGAGGTGTGGG[C/G]TGTATGGAGGTGTGG	113878
rs780588027	snp	A/G	2.59447e-05	0.00360162	missense	DTX2	GRCh38.p7	7:76505501	CAGAGATGGACCGCA[A/G]CATTACGGGCCACGG	113878
rs780747866	snp	A/G			downstream-variant-500B	DTX2	GRCh38.p7	7:76506336	CAGGTTCAAAGGTGC[A/G]ATGACTTGAACCAGG	113878
rs780763932	snp	A/G	1.83306e-05	0.00302737	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502485	CCCAGGGCGGAGGCG[A/G]GTGGCCCGCCCCCAC	113878
rs780820968	snp	A/G	0.000154226	0.00878004	missense	DTX2	GRCh38.p7	7:76492154	CTTTTCTCCCCCAGT[A/G]CCTCCCTCCCCAGCG	113878
rs780825417	snp	C/T	0.000169076	0.0091929	intron-variant	DTX2	GRCh38.p7	7:76501244	CCAGTACCCAGGGAC[C/T]CTTCACTTGTCTCTT	113878
rs780924836	snp	C/G	1.70461e-05	0.00291938	synonymous-codon, downstream-variant-500B	DTX2	GRCh38.p7	7:76502432	CCTGCTGTGCCTCCT[C/G]GCCATGTACTGCAAC	113878
rs780962381	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76464154	CATCCAGAAAGGGGA[C/T]GGTTAGAGGGAAGGT	113878
rs781140461	snp	A/G	1.65589e-05	0.00287736	missense	DTX2	GRCh38.p7	7:76482567	GCCCCTGGCCGAGGT[A/G]TCGTCTGGGAGTGGC	113878
rs781172309	snp	G/T	7.87495e-05	0.00627443	intron-variant	DTX2	GRCh38.p7	7:76505368	CCCCTCCTCCTCCCC[G/T]GGCAGGTCCTAGAGC	113878
rs781307590	snp	C/T	1.65154e-05	0.00287358	synonymous-codon, intron-variant	DTX2	GRCh38.p7	7:76497362	TGTTCTGATGTCAGC[C/T]ATTGGACTCCCTGTG	113878
rs781338210	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76505104	GAAGCAGGGAGGACT[C/T]GAGCATGGTGCCTGG	113878
rs781339036	snp	C/T	3.37952e-05	0.00411053	missense	DTX2	GRCh38.p7	7:76483056	GGCGCAGCTCCTCCT[C/T]CCCTGGGGAGCCAGC	113878
rs781397067	snp	C/T	3.3976e-05	0.00412151	missense, intron-variant	DTX2	GRCh38.p7	7:76503583	GCATTCCCCATGGTA[C/T]CCAGGTGAGGGGCCT	113878
rs781584052	snp	A/G	1.80175e-05	0.00300141	missense	DTX2	GRCh38.p7	7:76480541	GCCCTTCCCTGGTGC[A/G]GGTGTACACCAGCCC	113878
rs781764378	snp	C/T			downstream-variant-500B	DTX2	GRCh38.p7	7:76506034	ATGCGTGTGTGCGCA[C/T]TTGTGTGTGTGTGTG	113878
rs796171756	snp	A/T			intron-variant	DTX2	GRCh38.p7	7:76488950	AGGAAGGGGAGGAGC[A/T]TGCTCCAAATGAATG	113878
rs796267938	in-del	-/TT			intron-variant	DTX2	GRCh38.p7	7:76469361	AGCTTGAAATCTAGA[-/TT]TTTTTTTTTTTTTTT	113878
rs796315591	in-del	-/T			intron-variant	DTX2	GRCh38.p7	7:76469395	TACTGTGAATATTCC[-/T]TTTTTTTTTTTTTTT	113878
rs796351762	in-del	-/AT			intron-variant	DTX2	GRCh38.p7	7:76469360	AAGCTTGAAATCTAG[-/AT]TTTTTTTTTTTTTTT	113878
rs796441594	in-del	-/T			intron-variant	DTX2	GRCh38.p7	7:76481846	ATGGGTTTTTTTTTT[-/T]CGTGTTTGTTTGTTT	113878
rs796526977	snp	C/T			intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474503	TAGCTTTCATCTTCT[C/T]TCGGGACGGCAGAGG	113878
rs796570859	snp	C/G			intron-variant	DTX2	GRCh38.p7	7:76487189	CAGCCTCCTGAGTGG[C/G]CAGGACTACAGGCTT	113878
rs796662212	multinucleotide-polymorphism	CA/GG			intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474507	TTCATCTTCTCTCGG[CA/GG]CGGCAGAGGCAGGAC	113878
rs796905633	snp	G/T			intron-variant	DTX2	GRCh38.p7	7:76491146	GGGATTACAGGCGCC[G/T]GCCACCACGCCTGGC	113878
rs796963703	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76495942	CCAGATTCTCTTGAG[A/G]AAAACTGCACCTGTC	113878

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