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
rs7398	snp	A/G	0.468098	0.122202	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505817	ACTCATGGGGGCTTA[A/G]GATGCAGCTACCTCA	113878
rs723378	snp	C/T	0	0	intron-variant	DTX2	GRCh38.p7	7:76486163	GCACGAGCCTATCTA[C/T]GCGCTGAAAAACAGG	113878
rs723380	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76486232	TTAACCCTCCTCTGA[C/T]GGATGTAGAGCCAGA	113878
rs880777	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76477886	ACCttgagttattca[A/G]ccaaggtcacacata	113878
rs887044	snp	C/T	0.499325	0.0183582	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76479395	GGTGCCCTGAAGCAT[C/T]GCTAACCAAAAAGGA	113878
rs917425	snp	C/G	0.473818	0.111381	intron-variant	DTX2	GRCh38.p7	7:76500368	AGAGGGCGAGGAAGG[C/G]AAGGAAGAGGTCTAA	113878
rs1010933	snp	C/T	0	0	synonymous-codon	DTX2	GRCh38.p7	7:76505502	AGAGATGGACCGCAA[C/T]ATTACGGGCCACGGC	113878
rs1051646	snp	A/G			utr-variant-3-prime	DTX2	GRCh38.p7	7:76505906	GGTGTGGGGCGAGTA[A/G]AGACTTCCCCAGCCT	113878
rs1055094	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474928	CGTCAGGTCTTCGCC[A/G]CAAATCTCTGTCCAG	113878
rs1055096	snp	A/C	0.330714	0.236612	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474864	GTTCTACTGGAGATG[A/C]AATTTCATCCAAAAG	113878
rs1465314	snp	A/C	0.422158	0.181278	intron-variant	DTX2	GRCh38.p7	7:76504886	GCTCTACCCCTGGTG[A/C]TGGCCTGGGGGGCAC	113878
rs1467939	snp	C/T	0	0	intron-variant	DTX2	GRCh38.p7	7:76465462	ACTAACGTTCTGATC[C/T]TGTCTTTTACACACC	113878
rs1476932	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76467189	tagacatgagccacc[A/G]tgctcggcAGTGTTC	113878
rs1476934	snp	A/G	0	0	intron-variant	DTX2	GRCh38.p7	7:76467384	TCCCTGAGCCCtgct[A/G]ctgaatatctcctct	113878
rs1476935	snp	C/T	0	0	intron-variant	DTX2	GRCh38.p7	7:76467897	ATTCTCAGTGGGGGA[C/T]GAAGGGCATGAAACA	113878
rs1548823	snp	A/G	0	0	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505626	GCGGGGTGGCCACCA[A/G]AGGCGGGCGTGCTGG	113878
rs1613849	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76469017	AGCACTTCGGGAGGC[C/T]GAGGTGGGTGGATCA	113878
rs1614739	snp	C/T	0.5	0	intron-variant	DTX2	GRCh38.p7	7:76492403	CTCACTCTGGGGTGA[C/T]ACCATCACCAGAAAG	113878
rs1616563	snp	A/G	0	0	intron-variant	DTX2	GRCh38.p7	7:76469425	agcttgggcgacaga[A/G]tgagaatccgtctca	113878
rs1621319	snp	C/G	0.5	0	intron-variant	DTX2	GRCh38.p7	7:76499600	GGGACGGGGAGCCCA[C/G]TGCCACCCGTGGAGG	113878
rs1622742	snp	A/G	0.491936	0.0629843	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76476021	GCACTTTGGGAGGCC[A/G]AGGCGGGCGGATCGC	113878
rs1623251	snp	A/C/T	0.0541011	0.15593	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76475226	CCTCCCGGGTTCAAG[A/C/T]GATTCTTCTGCCTCA	113878
rs1627895	snp	A/G	0.483995	0.0880135	intron-variant	DTX2	GRCh38.p7	7:76481979	TGGGCATGACGGCTC[A/G]AGCCTGTAATCCCAA	113878
rs1628199	snp	C/T	0.483923	0.0882034	intron-variant	DTX2	GRCh38.p7	7:76481251	tgcagtgagccgaga[C/T]tgcgccactgcactc	113878
rs1628255	snp	C/T	0.483923	0.0882034	intron-variant	DTX2	GRCh38.p7	7:76481232	gccactgcactccag[C/T]ttaggcaacagagcc	113878
rs1631301	snp	A/C			intron-variant, utr-variant-5-prime	DTX2	GRCh38.p7	7:76462005	CCGATCCCCCCGACA[A/C]CCCCGATCTCCCGGG	113878
rs1631425	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76488820	ACCTCTCTGCCTCCC[A/G]GGCTCAAGCAATTCT	113878
rs1638067	snp	C/G	0	0	intron-variant	DTX2	GRCh38.p7	7:76487571	TGAGCATGGCAAGTC[C/G]CCTTCCCGAGCCTCA	113878
rs1638072	snp	C/T	0.498206	0.0298983	intron-variant	DTX2	GRCh38.p7	7:76484014	GCTGAAGTGCAGTGG[C/T]GCGATCACAGCTCAC	113878
rs1638073	snp	C/T	0.351492	0.228472	intron-variant	DTX2	GRCh38.p7	7:76483170	ACAGGGCAGACAAAA[C/T]GAGCGGCCGTTGCCC	113878
rs1638074	snp	A/G	0.495992	0.0445839	synonymous-codon	DTX2	GRCh38.p7	7:76482743	CCGCACGCTGCGGCA[A/G]AAGCTGGAAGTCTTG	113878
rs1638075	snp	C/G	0.308133	0.243155	synonymous-codon	DTX2	GRCh38.p7	7:76482677	GTTGTACCCCAGGGG[C/G]GCCAAGTCCACGAGC	113878
rs1638076	snp	C/G	0.483923	0.0882034	intron-variant	DTX2	GRCh38.p7	7:76482215	ATGACACCACACCCA[C/G]CTAACTTCAAATCGA	113878
rs1638077	snp	A/T	0	0	intron-variant	DTX2	GRCh38.p7	7:76500971	TGATCACGCCACTGC[A/T]CTGAGCCTGGGCGAC	113878
rs1638081	snp	A/G	0.486464	0.0811471	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76476871	CCCAATGGAGGGCGC[A/G]CCATGGCCCAGGCCC	113878
rs1638082	snp	A/G	0.5	0	intron-variant	DTX2	GRCh38.p7	7:76498716	CCCCAGCTCAGGGTC[A/G]CCCTCCGTGTGGCTG	113878
rs1638083	snp	C/G	0.485187	0.0847778	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474507	CCTGCCTCTGCCGTC[C/G]CGAGAGAAGATGAAA	113878
rs1638084	snp	C/T			intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76473898	CACAGAAATGTGGGA[C/T]GTTGTTTTTGACACA	113878
rs1638085	snp	C/T	0.5	0	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76473574	caagtgatctgccca[C/T]ctcggtctcctcaag	113878
rs1638086	snp	C/T	0.462582	0.131564	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76472903	CTAACTTCAGAAAAT[C/T]ATAGAAAAATTTTGA	113878
rs1638087	snp	C/T	0.332106	0.236133	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76472382	CCGAGAACTGCACCA[C/T]TGCACTCCAGCCTGG	113878
rs1638088	snp	G/T	0.456214	0.141336	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76472323	AAAACAAACCTCCCT[G/T]AAAATGCCAAACACT	113878
rs1638089	snp	C/T	0.375	0.216506	intron-variant, utr-variant-5-prime, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76470409	ATTACCTTGACTTCT[C/T]TGGGGACCCCAGTGT	113878
rs1638091	snp	A/G	0.4032	0.19756	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76470159	GGGCAGGGGCTCTGC[A/G]TACTATTCGATGAGA	113878
rs1638094	snp	A/G	0.486984	0.079614	intron-variant	DTX2	GRCh38.p7	7:76469133	TAGACCACAAGAACA[A/G]CCATAAACAATGTGT	113878
rs1638095	snp	A/G	0.491368	0.0651254	intron-variant	DTX2	GRCh38.p7	7:76469051	GGGGCTGAATGCGGT[A/G]GCTCACGCCTGTAAT	113878
rs1638096	snp	C/T	0.212425	0.24716	intron-variant	DTX2	GRCh38.p7	7:76468832	gaggctgcagtgagc[C/T]gagactgtgccactg	113878
rs1638101	snp	C/T	0.496616	0.0409947	intron-variant	DTX2	GRCh38.p7	7:76465227	CCCCATGACTCTGCT[C/T]CACCCTGAATCCCAC	113878
rs1638102	snp	A/G	0.362732	0.22314	intron-variant	DTX2	GRCh38.p7	7:76497540	CTGTGCAGAAGAGTC[A/G]GAGGCAGCGAGGCCG	113878
rs1638103	snp	C/T	0.5	0	intron-variant	DTX2	GRCh38.p7	7:76464245	GACTCCTCTCCCAGG[C/T]GACTGTGCCCCACTT	113878
rs1638119	snp	A/G	0	0	intron-variant	DTX2	GRCh38.p7	7:76495842	CGGCAACACTGCCTC[A/G]GCGGGCAGGCCTTCC	113878
rs1638120	snp	C/G	0.305186	0.243833	intron-variant	DTX2	GRCh38.p7	7:76500642	CCAAAGGGGCTGGAG[C/G]AAGGCCCTGGCACCC	113878
rs1638150	snp	A/G	0.375	0.216506	intron-variant	DTX2	GRCh38.p7	7:76494327	ACGGTGACTTCAGTG[A/G]GCAGGGACTTTCTGG	113878
rs1638151	snp	C/G	0.5	0	intron-variant	DTX2	GRCh38.p7	7:76493860	CTGCTCCTCAGTTGT[C/G]ACTGGCTGCACTCCA	113878
rs1638153	snp	C/T	0.277778	0.248452	intron-variant	DTX2	GRCh38.p7	7:76493649	CCCTCTCAGCCACTA[C/T]GACAGCAACTCCCCT	113878
rs1638154	snp	C/T	0.451359	0.148171	intron-variant	DTX2	GRCh38.p7	7:76492052	GGAGTCACTGAGGTG[C/T]CTTCGCGCTTTTACG	113878
rs1638155	snp	C/T	0.493748	0.0555599	intron-variant	DTX2	GRCh38.p7	7:76491615	AAAAAAGATATTTTA[C/T]ACTCACTAGTGTCAT	113878
rs1799127	snp	C/T	0.465683	0.126415	intron-variant	DTX2	GRCh38.p7	7:76498537	GAAAGCTCCCTTCTG[C/T]TCTGAAAAGCTGCAA	113878
rs1799148	snp	C/G	0	0	intron-variant	DTX2	GRCh38.p7	7:76494959	GCGTTTGCGCACAGG[C/G]TTTTTGCAGAGAGGT	113878
rs1799157	snp	C/T	0.277778	0.248452	intron-variant	DTX2	GRCh38.p7	7:76488741	TCTCTACTAAAAATA[C/T]AAAAATTAGCCAGGC	113878
rs1799158	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76488789	TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	113878
rs1799161	snp	A/G	0.375	0.216506	intron-variant	DTX2	GRCh38.p7	7:76496909	TGGAGCACACACAGC[A/G]CCCAGTGGAGGCTGG	113878
rs1799163	snp	A/T			intron-variant	DTX2	GRCh38.p7	7:76485555	TCCCTGAGCCTGGCT[A/T]GCCTATGTCTATGTC	113878
rs1799167	snp	C/T	0.5	0	intron-variant	DTX2	GRCh38.p7	7:76484582	TCCCTGGGACCAGGG[C/T]GGCCCCAGGCCCACC	113878
rs1799169	snp	A/G	0.498852	0.0239341	intron-variant	DTX2	GRCh38.p7	7:76484046	TTAAGACAGGGTCTC[A/G]CTCTGTCACCTAGGG	113878
rs1799171	snp	A/G	0.408163	0.193609	intron-variant	DTX2	GRCh38.p7	7:76483385	AGGCCCTTAATCATC[A/G]TGAGTGAAAGGACTG	113878
rs1799172	snp	G/T	0.451359	0.148171	intron-variant	DTX2	GRCh38.p7	7:76497754	TTTTGTAAGCAACAA[G/T]TTGTGGGTGAGAGGC	113878
rs1799173	snp	C/G	0.485049	0.0851591	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76480273	CTCTCACCCAGGCTA[C/G]AGTGCAGCAGTGTGA	113878
rs1799178	snp	C/T			intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76479710	GCAACCTCCACCTCC[C/T]GGGTAGGTTCAAGTG	113878
rs1799179	snp	A/T	0.467439	0.123371	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76479610	gtatttttagtagag[A/T]cggggtttcaccatg	113878
rs1799182	snp	C/T	0.466204	0.125522	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76478687	GGTGGCTCACACCTG[C/T]AATGCCAGTGTTTAG	113878
rs1799183	snp	C/T	0	0	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76477728	ACTGCAGCCCCATGG[C/T]CTCCTGGGCTAAAGC	113878
rs1799186	snp	A/G	0.485933	0.0826777	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76477244	GGCAGCTCTGTGGGT[A/G]CCAGGCCCGCCACGG	113878
rs1799187	snp	A/G	0.485866	0.0828688	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76477235	GTGGGTGCCAGGCCC[A/G]CCACGGAGCTGCCAA	113878
rs1799188	snp	C/T	0.49703	0.0384237	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76476872	CCCCAATGGAGGGCG[C/T]ACCATGGCCCAGGCC	113878
rs1799189	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76476402	TGAGCCTTCTGCTCC[A/G]GGGGCACAGGCACCT	113878
rs1799191	snp	A/G	0.5	0	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76472035	GCCAGTGCCTCCCAC[A/G]TCTTACTGGAAGATG	113878
rs1799192	snp	A/G	0.375	0.216506	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471322	TACAAAAAATTAGCC[A/G]GGCGCGGTGGCGGGT	113878
rs1799193	snp	A/T	0.375	0.216506	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471287	GTAGTCCCGGCTACT[A/T]GGGAGGCTGAGGCAG	113878
rs1799196	snp	A/T	0.49703	0.0384237	intron-variant	DTX2	GRCh38.p7	7:76467241	ACTGGTATAAGCACT[A/T]CATTCAGGAAATGGT	113878
rs1799197	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76465673	GAATCACTTGAACCC[A/G]GGAGGTGGAGGTTGC	113878
rs1799198	snp	A/G	0.442791	0.15916	intron-variant	DTX2	GRCh38.p7	7:76465471	GCTTCCTGAACTAAC[A/G]TTCTGATCTTGTCTT	113878
rs1799200	snp	A/G	0	0	intron-variant	DTX2	GRCh38.p7	7:76464698	TAAAATGTCCCTCAC[A/G]AGGCCAGGCACGGTG	113878
rs1799201	snp	A/G	0.495818	0.0455352	intron-variant	DTX2	GRCh38.p7	7:76464421	TAAAATGACCCTCAT[A/G]GAAATCTCCTAAAAT	113878
rs1799202	snp	C/G	0.4982	0.0299459	upstream-variant-2KB	DTX2	GRCh38.p7	7:76461569	AGGCGCACCTGCTCC[C/G]GTCTATGTTTTCTTC	113878
rs1799203	snp	A/G	0.46875	0.121031	upstream-variant-2KB	DTX2	GRCh38.p7	7:76459774	CAGGATCTGAGGAGT[A/G]TGGGGAGAAGCCGGG	113878
rs1978294	snp	C/T	0.420255	0.183066	intron-variant	DTX2	GRCh38.p7	7:76503060	GACACTAGGGAAGGC[C/T]GAGCCAGGCTCCGAT	113878
rs2005531	snp	A/G			intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76477757	gtgagtggtgattgc[A/G]gccactgcactctag	113878
rs2257223	snp	C/G	0.449345	0.150869	intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501515	TCCCTGCCTGGAACC[C/G]CCAGCAGGACCCCCA	113878
rs2258205	snp	A/G			intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76475676	tggcgacagagcaag[A/G]ctccttctcaaaaat	113878
rs2258686	snp	A/C/G	0.212077	0.24714	synonymous-codon	DTX2	GRCh38.p7	7:76482932	CCCCCAGCACCCCCC[A/C/G]CACAGGACCGCTTCT	113878
rs2258855	snp	A/C	0.497933	0.032082	intron-variant	DTX2	GRCh38.p7	7:76489896	TCATATTAAAAAAAA[A/C]AAAAACAACAACCTT	113878
rs2259255	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76482069	GTCAGCTCCCAAGTC[A/G]TTGCCTTCACAGTGT	113878
rs2260214	snp	C/T	0.5	0	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502136	AAGTGATCGGCCTCC[C/T]AGAGTGCTGGGATTA	113878
rs2260306	snp	C/G	0.0210502	0.100409	intron-variant	DTX2	GRCh38.p7	7:76504466	TGCCACCATGCGCCC[C/G]GGGGGTGGACGGGGC	113878
rs2260344	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76481620	CAATGTTTGGAGACA[C/T]TGTTGGTTGTT	113878
rs2261368	snp	C/G	0.5	0	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502011	CTTGCCTCAGCCTCC[C/G]GAGTAGCTGGGATTA	113878
rs2261681	snp	A/G	0.5	0	intron-variant	DTX2	GRCh38.p7	7:76466631	agtttcactcttatt[A/G]cctaggctggagtgc	113878
rs2261946	snp	C/T	0.5	0	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76472447	TTCTCCTGCCTCAGC[C/T]TCCCAGGTAGCTGGG	113878
rs2262041	snp	C/G	0.5	0	intron-variant	DTX2	GRCh38.p7	7:76500047	TTGAATCAAATCGTG[C/G]TGCCACAACGCCCCC	113878
rs2270253	snp	C/T	0.00664027	0.0572367	missense	DTX2	GRCh38.p7	7:76482916	TCCCTGCATACCCCG[C/T]CCCCCAGCACCCCCC	113878
rs2280611	snp	A/G	0.5	0	intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501661	ATGAGCTGGCTCCTC[A/G]TTCAGAACGTCCTCC	113878
rs2429285	snp	C/T	0.494568	0.0518327	intron-variant	DTX2	GRCh38.p7	7:76490142	gacggggtttcgcta[C/T]gttgcccaggatggt	113878
rs2429286	snp	C/G	0.48666	0.0805725	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76476227	TCATAATGAAGAACC[C/G]GCATCATTAGGAGCT	113878
rs2429290	snp	C/T	0.5	0	intron-variant	DTX2	GRCh38.p7	7:76494762	GGGGAGGCAGGAGTC[C/T]ACACAGCCTCCAGGC	113878
rs2430300	snp	G/T			intron-variant	DTX2	GRCh38.p7	7:76469481	cactgcaacctccac[G/T]tcttaggttcaagca	113878
rs2430301	snp	G/T	0.5	0	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76472989	ATTACCAAATTGTTT[G/T]CTTTTCCGTTTTTTT	113878
rs2430309	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76483201	GTTTCCGCTCTTAGC[C/T]GGGAAGACTCACCCC	113878
rs2430310	snp	A/C			intron-variant	DTX2	GRCh38.p7	7:76486814	GGCCCTGCAAAACGG[A/C]GCTCAGCTCTTGGTG	113878
rs2430312	snp	A/C	0.375	0.216506	intron-variant	DTX2	GRCh38.p7	7:76489899	TATTAAAAAAAAAAA[A/C]AACAACAACCTTTAT	113878
rs2430314	snp	C/T	0.498908	0.0233371	intron-variant	DTX2	GRCh38.p7	7:76490257	CTTGAACCTGGGAGG[C/T]AGAGGTTTCAGTGAG	113878
rs2462258	snp	C/T	0	0	intron-variant, synonymous-codon	DTX2	GRCh38.p7	7:76501290	GTCCATGAGAAAAAT[C/T]TGGTAAGTAAAGGTT	113878
rs2462259	snp	C/T	0	0	intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501400	CAGCTCTGTCTCGGC[C/T]CTGGTGTCCATCTGG	113878
rs2462260	snp	A/G			intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501840	TGGTAAGCCCTTCAG[A/G]GGCACAGGTCCCGGT	113878
rs2462302	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76469416	TTTTTTTTTTGAGAC[A/G]GATTCTCATTCTGTC	113878
rs2462305	snp	A/G			intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76475456	CTTTGGGAGGCTGAG[A/G]CGGGTGGATCACTTG	113878
rs2462309	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76481479	agcatgagccaccgc[A/G]cctggACCTGCAGTG	113878
rs2462311	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76481775	agtgaggaaacttga[A/G]aaacTGGTttttcct	113878
rs2462312	snp	A/G	3.38547e-05	0.00411415	missense	DTX2	GRCh38.p7	7:76482519	ATAGGCACCATGCGG[A/G]CTGTGCGGAGACACC	113878
rs2462313	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76486805	TGGCTCAGTGGCCCT[A/G]CAAAACGGCGCTCAG	113878
rs2530606	snp	A/C/G/T	0.487995	0.0765403	intron-variant	DTX2	GRCh38.p7	7:76488434	TGGGCTATGCAGCAG[A/C/G/T]CTAGGCAGCACTGGC	113878
rs2530607	snp	A/G	0	0	intron-variant	DTX2	GRCh38.p7	7:76488171	GCTCACCCTGCGAAT[A/G]GAGAGCAGGAACCAG	113878
rs2530609	snp	C/T	0.00542192	0.0517838	missense	DTX2	GRCh38.p7	7:76483042	GAAGGAGGAGCTGCG[C/T]CCCAGGCGTTGGTGG	113878
rs2530610	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76481148	GCAGAAACGCACACA[C/T]GCAGAGGGGCGCAGT	113878
rs2530616	snp	C/T			intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76475082	tgacctcaggtgatc[C/T]acctgccttggcctt	113878
rs2530619	snp	A/G	0.5	0	intron-variant	DTX2	GRCh38.p7	7:76498191	AGAGGACCTGCTGAG[A/G]TGACACAGACACTGA	113878
rs2530620	snp	A/C	0.5	0	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471154	AAAAAAAAAAAAAGA[A/C]CGAATGGAAACCAGA	113878
rs2530626	snp	A/G	0	0	intron-variant	DTX2	GRCh38.p7	7:76469330	TCCCTTGAAAATCAG[A/G]AAAGATGGCAATATT	113878
rs2530628	snp	C/T	0	0	intron-variant	DTX2	GRCh38.p7	7:76466964	gcagtgatccgtgat[C/T]atgccactgcactcc	113878
rs2530629	snp	C/T	0	0	intron-variant	DTX2	GRCh38.p7	7:76466929	gcctgggttacaagg[C/T]gagacactgtctcta	113878
rs2530630	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76466888	gaaaTAggccaggcg[C/T]ggtgcctcacgcctg	113878
rs2530631	snp	A/G	0	0	intron-variant	DTX2	GRCh38.p7	7:76466877	ggcgcggtgcctcac[A/G]cctgtaatcccagca	113878
rs2530632	snp	A/G	0.5	0	intron-variant	DTX2	GRCh38.p7	7:76466844	ttgggaggccgaggc[A/G]ggtggatcacctgag	113878
rs2530641	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76496408	TAGCCATCTCTTAAG[A/G]TGGCTTCCAGGGTCT	113878
rs2530648	snp	C/G/T	0.00159617	0.0282053	intron-variant	DTX2	GRCh38.p7	7:76494969	CTGGTTATAAACCTC[C/G/T]CTGCAAAAAGCCTGT	113878
rs2530652	snp	C/T	0.495745	0.0459295	intron-variant	DTX2	GRCh38.p7	7:76494537	CACACCCAGAGCACT[C/T]AGATCTGTGTCATGG	113878
rs2530654	snp	A/T	0.444444	0.157135	intron-variant	DTX2	GRCh38.p7	7:76493247	GAGCAAGATCCTGTC[A/T]CTTATAACAAGAAAA	113878
rs2539606	snp	A/G	0.375	0.216506	intron-variant	DTX2	GRCh38.p7	7:76465661	tcctggctcactgca[A/G]cctccacctcccggg	113878
rs2539607	snp	G/T			intron-variant	DTX2	GRCh38.p7	7:76465886	gcgcccggcAGGGAG[G/T]GGGTAAAGTGAGAGG	113878
rs2539617	snp	A/G			intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474447	ACTGCCAGAATCACA[A/G]AACCTAGAGAAGGGG	113878
rs2539618	snp	C/T					GRCh38.p7	7:76474495	CCACCCAGTAGCTTT[C/T]ATCTTCTCTCGGGAC	113878
rs2539619	snp	C/G	0	0	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474563	AAGGATTAGTTGTAA[C/G]AGATTTCAGCAGGTC	113878
rs2539628	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76478852	GGCACTCCAACAGCC[A/G]GTGCCCTGGGGGGCA	113878
rs2539633	snp	C/T					GRCh38.p7	7:76481016	AGCAGAAATGCCTGT[C/T]CCGACCACAGAGGTT	113878
rs2539640	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76486498	CGTGCACAGCTTCCA[C/T]GTGCCCCCTGGGAAC	113878
rs2539641	snp	A/G	0.5	0	intron-variant	DTX2	GRCh38.p7	7:76486658	CTAAATGTGTCATGC[A/G]TGCTCTTGTCTCCCT	113878
rs2539643	snp	G/T	0.494774	0.0508504	intron-variant	DTX2	GRCh38.p7	7:76486883	gctgctgctgctgct[G/T]ctgcCCTTGCCTCTA	113878
rs2539644	snp	C/T	0.494774	0.0508504			GRCh38.p7	7:76486884	ctgctgctgctgctg[C/T]tgcCCTTGCCTCTAA	113878
rs2539646	snp	C/T	0.42	0.183303			GRCh38.p7	7:76488501	TCTGGGCTCCAACTA[C/T]GGGCTTGAGCTCAGT	113878
rs2539648	snp	C/T	0.5	0			GRCh38.p7	7:76494005	AGCCCTTGGCAGAGC[C/T]GAGACACAGCCCCGG	113878
rs2539654	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76498853	gtgtgtggggtgtgt[A/G]gaggtgagggtgtgt	113878
rs2690526	snp	A/G	0.491732	0.0637633	intron-variant	DTX2	GRCh38.p7	7:76503645	TCCCACCCCGCCCAC[A/G]TCCCAGCAGTCTGCC	113878
rs2690527	snp	A/G	0.0543475	0.155628	intron-variant	DTX2	GRCh38.p7	7:76503724	GTCCCCTAAGGCCAG[A/G]GCCATGGAGGGCCGG	113878
rs2690569	snp	C/T	0.375	0.216506	intron-variant	DTX2	GRCh38.p7	7:76496433	GAGAAAGGGGAAGCC[C/T]AGAGCTTCTTAGCCA	113878
rs2690570	snp	C/T	0	0	intron-variant	DTX2	GRCh38.p7	7:76496415	AGCTTCTTAGCCATC[C/T]CTTAAGGTGGCTTCC	113878
rs2690576	snp	C/T	0.5	0	intron-variant	DTX2	GRCh38.p7	7:76493797	CAACCCCCCGCCTGA[C/T]GGCTCATGCCTCTGA	113878
rs2690578	snp	G/T	0.375	0.216506	intron-variant	DTX2	GRCh38.p7	7:76498768	CCCGAACCCAAATCC[G/T]GTCACGGTGGCGAGA	113878
rs2690581	snp	A/G	0.5	0	intron-variant	DTX2	GRCh38.p7	7:76486452	TTTTCAATTTCACGC[A/G]CTCACATGGTATTTC	113878
rs2690583	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76483307	CAGGTAGGCTCTGGA[C/T]GGCCACGGCACCTCG	113878
rs2690587	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76481057	GCACCACCTCCATGC[C/T]GGCCTGCCGGCCAAA	113878
rs2690589	snp	C/T	6.74593e-05	0.00580733	missense	DTX2	GRCh38.p7	7:76480621	CGATGAAGCTGCAGA[C/T]GGTGGCACTGTAGGG	113878
rs2690600	snp	C/T	0	0	intron-variant	DTX2	GRCh38.p7	7:76464867	TTCAGTTCTCTATGT[C/T]CACTTTATCTCTTCA	113878
rs2690601	snp	A/T			intron-variant	DTX2	GRCh38.p7	7:76464715	GTTCCAGTGTGCTCC[A/T]TTAAAATGTCCCTCA	113878
rs2690625	snp	A/C	0	0	intron-variant	DTX2	GRCh38.p7	7:76499478	AGAATTCTCTGCAGC[A/C]CCTGAAGGCCGTGAG	113878
rs2690626	snp	A/G	0	0	intron-variant	DTX2	GRCh38.p7	7:76499482	TTCTCTGCAGCCCCT[A/G]AAGGCCGTGAGCTTG	113878
rs2690636	snp	C/T	0.5	0	intron-variant	DTX2	GRCh38.p7	7:76498291	GCTGGAGGTCGGACA[C/T]GATCGGAAGCCACCC	113878
rs2690664	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76501075	AGAACCTGAACCTCT[A/G]CTGAGCCACGTTTTG	113878
rs2690683	snp	A/G	0.499913	0.00659276	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502269	CAGCCCACTGTTGGC[A/G]AGCATGACCCATGTT	113878
rs2903802	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76481336	agccaggtgtggtgg[C/T]ggatgcctataatcc	113878
rs2903803	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76481289	tgaggcaggagaatc[A/G]cttgaacccaggagg	113878
rs3748133	snp	C/T	0.00676609	0.0577691	intron-variant	DTX2	GRCh38.p7	7:76505264	GGAGTGGATGAGTCA[C/T]CTGGGAGGGGCTGGG	113878
rs3748135	snp	A/G	0.337386	0.23423	downstream-variant-500B	DTX2	GRCh38.p7	7:76506023	TGTGTGCATGCATGC[A/G]TGTGTGCGCACTTGT	113878
rs3972782	snp	A/C	0.372592	0.217879	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474515	CTGGCTGTCCTGCCT[A/C]TGCCGTCCCGAGAGA	113878
rs3972783	snp	C/T	0.327445	0.237702	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474514	TGGCTGTCCTGCCTC[C/T]GCCGTCCCGAGAGAA	113878
rs3972896	snp	G/T	0.496483	0.0417852	intron-variant	DTX2	GRCh38.p7	7:76491411	agtcccagctattca[G/T]taggctgaggcagga	113878
rs4236506	snp	A/G	0.37124	0.218634	synonymous-codon	DTX2	GRCh38.p7	7:76482518	AATAGGCACCATGCG[A/G]GCTGTGCGGAGACAC	113878
rs4236507	snp	A/C	0.445196	0.1562	intron-variant	DTX2	GRCh38.p7	7:76502953	ACACATGAAGAGCCG[A/C]GCCCAGACTGACCCC	113878
rs4368901	snp	C/T	0.0807149	0.183963	intron-variant	DTX2	GRCh38.p7	7:76466786	tatttttagtagaga[C/T]ggagtttctccatgt	113878
rs4618620	snp	C/T	0.078151	0.181571	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76480079	ttgggaaggctgagg[C/T]gagtctatcccttga	113878
rs4727187	snp	A/C	0.448323	0.15221	intron-variant	DTX2	GRCh38.p7	7:76503156	CAAATGCGATTCACC[A/C]GTGGAGATTTCTGCT	113878
rs4728773	snp	C/T	0.447809	0.152878	intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501744	CCTTGTAAGACCCCA[C/T]GCCGAGGGCCTCCCC	113878
rs4728774	snp	C/T	0.5	0	intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501852	CAGAGGCACAGGTCC[C/T]GGTGACTCACCTGTG	113878
rs4728775	snp	A/G	0.441461	0.160757	synonymous-codon, downstream-variant-500B	DTX2	GRCh38.p7	7:76502378	GGCAATCGGGTCCCT[A/G]GCTGTGGGCCACCTC	113878
rs4728783	snp	C/T	0.449091	0.151204	downstream-variant-500B	DTX2	GRCh38.p7	7:76506360	AACCAGGCATGGTGA[C/T]GCATGCCTGTTATCC	113878
rs6465152	snp	A/G	0.451608	0.147832	intron-variant	DTX2	GRCh38.p7	7:76491187	agttttagtagagac[A/G]ggattttgccatctt	113878
rs6465153	snp	A/G	0.493201	0.0579089	intron-variant	DTX2	GRCh38.p7	7:76491535	tgatccacctgcctc[A/G]gcctcccaaagtgct	113878
rs6958774	snp	A/G	0.441063	0.16123	synonymous-codon, downstream-variant-500B	DTX2	GRCh38.p7	7:76502333	GAAGCTGTCCACAGC[A/G]TCTGGATACAGCGAT	113878
rs6963784	snp	C/G	0.472104	0.114789	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502495	AGGCGGGTGGCCCGC[C/G]CCCACAGTCCTGAGC	113878
rs6964085	snp	C/G	0.5	0	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502657	TCTTCTAGGTCTGCC[C/G]CACACTTTAGAAAGG	113878
rs6965836	snp	C/G			intron-variant	DTX2	GRCh38.p7	7:76491212	catcttggccaggct[C/G]gtcttgaactcctga	113878
rs6966793	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76491154	aggcgcctgccacca[C/T]gcctggctaattttt	113878
rs6966938	snp	C/G/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76491215	cttggccaggctggt[C/G/T]ttgaactcctgacct	113878
rs6979487	snp	A/G	0.374445	0.216826	missense, downstream-variant-500B	DTX2	GRCh38.p7	7:76502328	ATGGAGAAGCTGTCC[A/G]CAGCGTCTGGATACA	113878
rs7456609	snp	C/T			intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474186	gcctACttttttttt[C/T]ctttttctttttctt	113878
rs7799234	snp	C/T	0.432651	0.170701	downstream-variant-500B	DTX2	GRCh38.p7	7:76506086	AGAGCAAGAGGGGGT[C/T]CCATGGGCTCATCGG	113878
rs7807719	snp	A/C	0.44858	0.151875	intron-variant	DTX2	GRCh38.p7	7:76505116	ACTCGAGCATGGTGC[A/C]TGGGCATCAGGACCA	113878
rs10247123	snp	A/G	0.0036324	0.0424618	intron-variant	DTX2	GRCh38.p7	7:76483163	GTATCGTGGGCAACG[A/G]CCGCTCGTTTTGTCT	113878
rs10257113	snp	A/C	0.0178098	0.0926698	intron-variant	DTX2	GRCh38.p7	7:76502756	CCCAGGGCACCGCCT[A/C]CCCCTCGGCCACTTG	113878
rs10588542	in-del	-/TGTA			intron-variant	DTX2	GRCh38.p7	7:76498789	TGGGTTCGGGCAGTC[-/TGTA]TGGGTGTGTGGAGGT	113878
rs11308718	in-del	-/T	0.499703	0.0121769	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474224	TCTTTCTTTCTTTTC[-/T]TTTTTTTTTTTTAAG	113878
rs11320055	in-del	-/T	0.486464	0.0811471	intron-variant	DTX2	GRCh38.p7	7:76481190	CGATGTGTTTTGATC[-/T]TTTTTTTTTTTTTTG	113878
rs11980492	snp	C/T	0.448066	0.152544	intron-variant	DTX2	GRCh38.p7	7:76504919	GTTCTGAGCGCCCAG[C/T]GAAGCCACGGAGGTG	113878
rs12534498	snp	A/G	0.0280485	0.115055	missense	DTX2	GRCh38.p7	7:76482621	GCCTATGAAGCCAGC[A/G]TCTGTGACTATCTGG	113878
rs13236917	snp	A/T	0.375	0.216506	upstream-variant-2KB	DTX2	GRCh38.p7	7:76460354	attattattattatt[A/T]ttttttttttttttt	113878
rs17855260	snp	C/T	0.469784	0.119142	synonymous-codon, intron-variant	DTX2	GRCh38.p7	7:76503581	CAGCATTCCCCATGG[C/T]ATCCAGGTGAGGGGC	113878
rs28405799	snp	C/G	0	0	upstream-variant-2KB	DTX2	GRCh38.p7	7:76460514	CCACCACTACGCCCG[C/G]TTAATTTTTTTTTTT	113878
rs28412600	snp	A/C	0.5	0	intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501649	GCTTTAGTGCCCATG[A/C]GCTGGCTCCTCGTTC	113878
rs28437796	snp	C/T			upstream-variant-2KB	DTX2	GRCh38.p7	7:76460330	ACGCGCCACCACACC[C/T]AGTTAATTATTATTA	113878
rs28449857	snp	C/T	0	0	intron-variant, utr-variant-5-prime, upstream-variant-2KB	DTX2	GRCh38.p7	7:76477157	ACCATTCCGCCCGCC[C/T]GCCCGCCCGAGGGCA	113878
rs28483714	snp	G/T			intron-variant	DTX2	GRCh38.p7	7:76499017	GTGTGTAGAAGTGTG[G/T]GGTGTGTGAGGTGGG	113878
rs28533048	snp	G/T			intron-variant	DTX2	GRCh38.p7	7:76499020	TGTAGAAGTGTGGGG[G/T]GTGTGAGGTGGGGTG	113878
rs28538438	snp	A/G	0.451732	0.147663	intron-variant	DTX2	GRCh38.p7	7:76503080	TCCCTAGTGTCTGCC[A/G]TCCTGGGCAGCCAGG	113878
rs28714524	snp	C/T	0	0	upstream-variant-2KB	DTX2	GRCh38.p7	7:76460515	CACCACTACGCCCGC[C/T]TAATTTTTTTTTTTT	113878
rs35538069	snp	C/T	0.454784	0.1434	intron-variant	DTX2	GRCh38.p7	7:76499368	GGTGGCGTGGTGGGG[C/T]GGAGGCTGGAGTCGG	113878
rs55746915	snp	C/T			utr-variant-3-prime	DTX2	GRCh38.p7	7:76505937	GGACGGGCGTGGGTT[C/T]TGGGTCAGCTTCTTT	113878
rs55921935	snp	C/T			utr-variant-3-prime	DTX2	GRCh38.p7	7:76505773	CTCTCCTCCTCCCCT[C/T]TGGGAATTGGGCAGC	113878
rs56035536	snp	C/T	0.000253582	0.0112573	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505855	GGGCCCGTCTGTCCT[C/T]TGGGGGCTGCTTCGG	113878
rs57638500	snp	A/G	0.084364	0.187256	intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501814	CTGCTGTCATGTCGG[A/G]CCTGTGCTGCTGGTA	113878
rs57655854	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76499130	AGCTGTGTGGGGTGT[A/G]TGGAGGTGTAGGGTG	113878
rs57887395	in-del	-/GGC/GGCTGCTGCTGCTGC			intron-variant	DTX2	GRCh38.p7	7:76486848	TCTGTTGTGGTGGGC[-/GGC/GGCTGCTGCTGCTGC]TGCTGCTGCTGCTGC	113878
rs58029674	snp	C/T	0.00755907	0.0610114	intron-variant	DTX2	GRCh38.p7	7:76503290	TTGGAAGCCAGTTTC[C/T]GGGCAGGAGGCTGCC	113878
rs58734174	snp	A/G	0.5	0	intron-variant	DTX2	GRCh38.p7	7:76499663	TTCTGTGGTTCTGCT[A/G]CTCCCACTACCTAGA	113878
rs58741690	snp	A/C			intron-variant	DTX2	GRCh38.p7	7:76487264	GGTCTCACTATATTG[A/C]CCAGGCTGGTCCCAA	113878
rs58883565	snp	C/G			intron-variant	DTX2	GRCh38.p7	7:76499136	GTGGGGTGTATGGAG[C/G]TGTAGGGTGTGAGGA	113878
rs58971525	snp	C/G			intron-variant	DTX2	GRCh38.p7	7:76499058	TGTGGAGGTGGGTGT[C/G]TGGAGCTGTGTGTGG	113878
rs59102620	snp	A/G	0.00795532	0.062565	intron-variant	DTX2	GRCh38.p7	7:76503180	TTCTGCTCAGGATCC[A/G]AGTTTTCCCACTCGC	113878
rs59141704	snp	G/T			intron-variant	DTX2	GRCh38.p7	7:76499071	GTGTGGAGCTGTGTG[G/T]GGTGTGTGGAGGTGT	113878
rs59218104	snp	A/G	0.0287789	0.116453	synonymous-codon	DTX2	GRCh38.p7	7:76482806	CATCATCGCTCCGCC[A/G]GGCCACACAGGCGTC	113878
rs59266144	snp	G/T			intron-variant	DTX2	GRCh38.p7	7:76499154	TAGGGTGTGAGGAGG[G/T]GTGGAGGTGTGGGGT	113878
rs59479345	snp	C/T	0.0836354	0.186609	intron-variant	DTX2	GRCh38.p7	7:76481923	GGCTGGTCTTCAACT[C/T]CTGAGCTCAAGTGAT	113878
rs59534834	snp	G/T			intron-variant	DTX2	GRCh38.p7	7:76499076	GAGCTGTGTGTGGTG[G/T]GTGGAGGTGTGAGGT	113878
rs59594095	in-del	-/TTTTGC			intron-variant	DTX2	GRCh38.p7	7:76486887	TGCTGCTGCTGCTGC[-/TTTTGC]CCTTGCCTCTAAAAG	113878
rs59997938	snp	A/T			intron-variant	DTX2	GRCh38.p7	7:76499115	GTGTGGGGTGTGTGG[A/T]GCTGTGTGGGGTGTA	113878
rs60006089	snp	A/G	0.000165349	0.00909106	missense	DTX2	GRCh38.p7	7:76482819	CCGGGCCACACAGGC[A/G]TCGCCTGCTCTTGCC	113878
rs60078111	snp	G/T			intron-variant	DTX2	GRCh38.p7	7:76499124	GTGTGGAGCTGTGTG[G/T]GGTGTATGGAGGTGT	113878
rs60347271	snp	G/T			intron-variant	DTX2	GRCh38.p7	7:76499135	TGTGGGGTGTATGGA[G/T]GTGTAGGGTGTGAGG	113878
rs60411665	in-del	-/TG			intron-variant	DTX2	GRCh38.p7	7:76499016	GTGTGTAGAAGTGTG[-/TG]GGGTGTGTGAGGTGG	113878
rs60539801	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76468149	ACGCCCGGTGTGGCT[C/T]TGGGGAGCACCTGGG	113878
rs60782153	snp	C/T	0.0836354	0.186609	intron-variant	DTX2	GRCh38.p7	7:76481018	CAGAAATGCCTGTCC[C/T]GACCACAGAGGTTGA	113878
rs60815284	snp	G/T			intron-variant	DTX2	GRCh38.p7	7:76499047	GGTGTGAGGTGTGTG[G/T]AGGTGGGTGTGTGGA	113878
rs60859861	in-del	-/C/CC/CCC	0	0	downstream-variant-500B	DTX2	GRCh38.p7	7:76506058	TGTGTGCCCCCCCCC[-/C/CC/CCC]ACTTCCTGCATCAGA	113878
rs61549812	snp	C/T	0.438105	0.164671	intron-variant	DTX2	GRCh38.p7	7:76503757	ATGGGGAGGCAGTGC[C/T]GGGGCTTAGGGTAAG	113878
rs61570712	snp	C/T	0.0821764	0.185298	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474906	ATGGTGCCTCAGCCA[C/T]GATCCTCTGGACAGA	113878
rs61647172	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76499088	GTGTGTGGAGGTGTG[A/G]GGTGTGTGGAGGTGT	113878
rs62475625	snp	A/C			upstream-variant-2KB	DTX2	GRCh38.p7	7:76460646	AGCCACTGCGCCCGG[A/C]CTCCACACCCAGTTA	113878
rs62475626	snp	G/T			intron-variant	DTX2	GRCh38.p7	7:76464152	CACATCCAGAAAGGG[G/T]ACGGTTAGAGGGAAG	113878
rs62475630	snp	A/T	0.353371	0.227628	intron-variant, downstream-variant-500B	DTX2, FDPSP2	GRCh38.p7	7:76469908	CAGTTGTGGTATGGA[A/T]ATATCCCGCTTCCCC	113878
rs62475631	snp	C/G			intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76470878	AAGCTTGCAGCAGTT[C/G]CGCATACCAGCCCAC	113878
rs62475632	snp	C/T			intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471230	GCAGTGGCGCGATCT[C/T]GGCTCACTGCAAACT	113878
rs62475634	snp	A/G	0.322959	0.239117	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76472482	CAGGTGCATGCCACC[A/G]TGCCCAGCTAATTTT	113878
rs62475646	snp	A/G	0.32955	0.237006	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76475271	AGCCGAGATCACGCC[A/G]TTGCACTCCAGCCTG	113878
rs62475647	snp	A/G			intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76476017	TCAAGCGATCCGCCC[A/G]CCTCGGCCTCCCAAA	113878
rs62475650	snp	A/C	0.490175	0.0693959	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76477666	AGTTGAGTATGGTGG[A/C]ACATGCCTGTAGTCC	113878
rs62475652	snp	C/T			intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76480034	AAGCGTGAGACCAGG[C/T]GCGGTGGCTCACACC	113878
rs62475653	snp	G/T	0.33693	0.2344	intron-variant	DTX2	GRCh38.p7	7:76481706	TGCTGCTCGCCATCC[G/T]GCAGTGCACTGGGCT	113878
rs62475656	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76486810	CAGTGGCCCTGCAAA[A/G]CGGCGCTCAGCTCTT	113878
rs62476489	snp	G/T			intron-variant	DTX2	GRCh38.p7	7:76501133	TTTAGCTGGGAGCCC[G/T]GGAGATACTGTTGGG	113878
rs62476491	snp	G/T			intron-variant	DTX2	GRCh38.p7	7:76503174	GGAGATTTCTGCTCA[G/T]GATCCGAGTTTTCCC	113878
rs62476492	snp	C/G			intron-variant	DTX2	GRCh38.p7	7:76503807	AAAAGGCTGGCCCTC[C/G]ACTCTTTCCTGAACC	113878
rs62476493	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76504267	TCGGGGTTGGCATCT[C/T]GGAGCGGGGGAGGAG	113878
rs62476494	snp	C/G/T	0.346372	0.230678	intron-variant	DTX2	GRCh38.p7	7:76504312	GGGCCTGTCCCTGTG[C/G/T]GGGCTCTCGGAGCAC	113878
rs62476495	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76504546	AGCGGAGGACAGAGG[C/T]TGAGGCCGGGCCGAG	113878
rs62476496	snp	A/T			intron-variant	DTX2	GRCh38.p7	7:76504773	GTGGTGTCTGCACTG[A/T]GACATGAATAGGGAC	113878
rs62476497	snp	G/T	0.325091	0.238456	downstream-variant-500B	DTX2	GRCh38.p7	7:76506083	ATCAGAGCAAGAGGG[G/T]GTTCCATGGGCTCAT	113878
rs66658628	in-del	-/TGTT			intron-variant	DTX2	GRCh38.p7	7:76481849	GGTTTTTTTTTTTCG[-/TGTT]TGTTTGTTTGTTTGT	113878
rs66718202	in-del	-/T			intron-variant	DTX2	GRCh38.p7	7:76466593	TTGTTTCTCTGTCTC[-/T]TTTTTTTTTTTCTTT	113878
rs66725205	in-del	-/T	0.458084	0.138567	intron-variant	DTX2	GRCh38.p7	7:76498918	GGAGTGTGTGTGGAG[-/T]GTGTGTGGAGGTGTG	113878
rs67541833	in-del	-/AT			intron-variant	DTX2	GRCh38.p7	7:76469360	AGCTTGAAATCTAGA[-/AT]TTTTTTTTTTTTTTT	113878
rs67632183	in-del	-/G	0.111224	0.207945	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502201	TGTGCTGAAATGCTG[-/G]AAGTGCAGTCAAAGT	113878
rs71085418	in-del	-/AAAAAA	0	0	upstream-variant-2KB	DTX2	GRCh38.p7	7:76460533	CTCTACTAAAAATAC[-/AAAAAA]AAAAAAAAAAAAAAA	113878
rs71229518	multinucleotide-polymorphism	CGGTGCCTCACA/TGGTGCCTCACG	0.5	0	intron-variant	DTX2	GRCh38.p7	7:76466877	GAAATAGGCCAGGCG[CGGTGCCTCACA/TGGTGCCTCACG]CCTGTAATCCCAGCA	113878
rs71552450	snp	A/C	0.000335413	0.0129458	intron-variant	DTX2	GRCh38.p7	7:76492265	GCAGGTAGGTGCCTG[A/C]CCTCGGGCTGCAGAG	113878
rs71562434	snp	A/C	0.00676609	0.0577691	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76480228	GAGGATTGCTTGAGA[A/C]CAGGAGTTTGAGGCT	113878
rs71562435	snp	A/G	0.0919752	0.193722	intron-variant	DTX2	GRCh38.p7	7:76481111	GTCCCACCACTCAGT[A/G]GCTGTGTGCCCTGGG	113878
rs71562436	snp	A/G	0.5	0	intron-variant	DTX2	GRCh38.p7	7:76482029	TCCAGGAGTGTCGTA[A/G]AGTCTGTGAAAACTG	113878
rs73140090	snp	C/G	0.109809	0.206994	intron-variant	DTX2	GRCh38.p7	7:76505356	TCCTTCCTCTTCCCC[C/G]TCCTCCTCCCCGGGC	113878
rs73363181	snp	C/T	0.0593169	0.161679	synonymous-codon	DTX2	GRCh38.p7	7:76505412	CTGGAAGAGGCGGCT[C/T]ATCTTCACAGTGGGC	113878
rs73703176	snp	C/G	0.0115144	0.0749975	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76480399	GTGCATTGGTAACTG[C/G]TCATGTCTGTCCTGT	113878
rs73703177	snp	A/G	0.499918	0.00638925	intron-variant	DTX2	GRCh38.p7	7:76495931	GCGCAGAGGCACCAG[A/G]TTCTCTTGAGGAAAA	113878
rs73703178	snp	A/G	0.0174175	0.0916809	intron-variant	DTX2	GRCh38.p7	7:76499286	TTCCCGTTTGAGATC[A/G]GGGAACCGAGGCTCA	113878
rs73703179	snp	A/G	0.304701	0.243942	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502247	CCAAGACTGGCCCAC[A/G]TCAGCCCAGCCCACT	113878
rs73703182	snp	C/G	0.0115547	0.0751255	synonymous-codon, intron-variant	DTX2	GRCh38.p7	7:76503488	GACGGGGACCCAGCC[C/G]CAGGGAAAGATGGAG	113878
rs73703183	snp	A/G	0.0314385	0.121371	intron-variant	DTX2	GRCh38.p7	7:76504718	GACAGGCAGGGACCG[A/G]GGGCTGTGTTAGACC	113878
rs73703185	snp	A/G	0.0188781	0.095303	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505922	AGACTTCCCCAGCCT[A/G]GACGGGCGTGGGTTC	113878
rs74325932	snp	C/G			intron-variant	DTX2	GRCh38.p7	7:76495047	TGACAGTGCCTCCAG[C/G]TGACAGCTCCCCTGG	113878
rs74908045	snp	C/T	0	0	intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501903	CTTTTTTTTTTTTTT[C/T]TCTGAGACGGAGTCT	113878
rs75142968	snp	A/T			downstream-variant-500B	DTX2	GRCh38.p7	7:76506008	CCAGCAGGTCCTGAG[A/T]GTGTGCATGCATGCG	113878
rs77036139	snp	G/T	0.126564	0.217402	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76472156	GTGGAGCTCGGGGAT[G/T]GGGGGATGTGTCTGC	113878
rs77283929	snp	C/T	0.5	0	intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501905	TTTTTTTTTTTTTTT[C/T]TGAGACGGAGTCTCG	113878
rs78788541	snp	C/T	0.48818	0.0759629	intron-variant	DTX2	GRCh38.p7	7:76488153	TTTCTACAGAACATT[C/T]TCCTGGTTCCTGCTC	113878
rs79153110	snp	G/T	0.5	0	intron-variant	DTX2	GRCh38.p7	7:76486849	TCTGTTGTGGTGGgc[G/T]gctgctgctgctgct	113878
rs79750972	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76483346	TACCTGAGTCCTGGC[A/G]GTCACCACACGGGTT	113878
rs79848975	snp	A/T	0.488786	0.0740357	intron-variant	DTX2	GRCh38.p7	7:76488125	ATGGGGGAAGTGGTG[A/T]CATTTTTAGAGCTTT	113878
rs80344060	snp	C/T	0	0	intron-variant	DTX2	GRCh38.p7	7:76488186	TATTCGCAGGGTGAG[C/T]GCCCACTGGAAGCCT	113878
rs111304404	snp	A/C			intron-variant	DTX2	GRCh38.p7	7:76493268	GATCTTGCTCTGTTC[A/C]CCAGGCTGGTGTGCA	113878
rs111308286	snp	A/G	0.0260105	0.111035	intron-variant	DTX2	GRCh38.p7	7:76469166	GGCAGAGTCACTGCA[A/G]AGACTTTTTCTGTCC	113878
rs111534570	snp	A/G			intron-variant, downstream-variant-500B	DTX2, FDPSP2	GRCh38.p7	7:76469576	TTTTTGTATTTTTTA[A/G]TAGAGACAGGGTTTC	113878
rs111861716	snp	G/T			intron-variant, downstream-variant-500B	DTX2, FDPSP2	GRCh38.p7	7:76469725	AACATCAGCTCAGTT[G/T]TTAAAAGCCAAACCT	113878
rs111922570	snp	C/G	0.5	0	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76475134	caacatggtgaagcc[C/G]cgtctctactaaata	113878
rs112023990	in-del	-/GG	0.5	0	downstream-variant-500B	DTX2	GRCh38.p7	7:76506083	ATCAGAGCAAGAGGG[-/GG]TTCCATGGGCTCATC	113878
rs112174566	snp	C/T	0.089084	0.191327	downstream-variant-500B	DTX2	GRCh38.p7	7:76506494	AGGTGCAGTGGCTCA[C/T]GCCTCTAATCCTAGC	113878
rs112371280	snp	A/G	0	0	intron-variant	DTX2	GRCh38.p7	7:76505058	CACCAGGGAGGGTGG[A/G]TGGGCGGGCGCTCGT	113878
rs112706472	in-del	-/ATT	0.5	0	intron-variant	DTX2	GRCh38.p7	7:76491267	TCCCAAAGTGCTGAG[-/ATT]ATAGGCGTGAGCCAC	113878
rs112928973	snp	C/T			intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76470799	ATGCCCAGCTTCTGA[C/T]ACCAGGAGATCTGTC	113878
rs112943563	snp	A/G	0.0788843	0.182262	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76472887	AGTGAATAGCTTCAC[A/G]TCAAAATTTTTCTAT	113878
rs113065010	snp	G/T			intron-variant	DTX2	GRCh38.p7	7:76468741	TGGGATTATAGGCGT[G/T]AGCCACCACGCCCAG	113878
rs113066563	in-del	-/A	0.5	0	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76475010	ACTAAAAAAAAGAAG[-/A]AAAAAAAAAACTTTG	113878
rs113186985	snp	A/C			intron-variant	DTX2	GRCh38.p7	7:76484097	GCCTGTAGTTCCAGC[A/C]CTTTGGGAGGCCGAG	113878
rs113190194	snp	C/T	0.215446	0.2476	intron-variant	DTX2	GRCh38.p7	7:76505081	GCGCTCGTCCAGCAA[C/T]GGCTGTGGAAGCAGG	113878
rs113440354	snp	A/G	0.0836354	0.186609	intron-variant	DTX2	GRCh38.p7	7:76482094	CAGTGTGTGAAGTCA[A/G]CTGAGAAAGATAGCA	113878
rs113457633	snp	A/G	0	0	intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501842	GTAAGCCCTTCAGAG[A/G]CACAGGTCCCGGTGA	113878
rs113506813	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76498987	TGAGGTGTGTGGAGG[A/G]GTGAGGTGTGTAGGG	113878
rs113507079	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76466600	TCTGTCTCTTTTTTT[C/T]TTTTCTTTGAGGCAG	113878
rs113540239	snp	G/T	0.5	0	intron-variant	DTX2	GRCh38.p7	7:76499628	CCCTCTTTCACCCCC[G/T]CACGGGCTTGGCTGC	113878
rs113549464	snp	C/T			intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76470740	TCAGCAGGCAGTAGA[C/T]ACATGCTTCCAGAAG	113878
rs113613956	snp	A/T			intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76479593	GAGACCAGCCTGGCC[A/T]ACATGGTGAAACCCC	113878
rs113825285	snp	C/T	0.0818113	0.184966	intron-variant	DTX2	GRCh38.p7	7:76483345	GTACCTGAGTCCTGG[C/T]GGTCACCACACGGGT	113878
rs113825695	snp	C/G	0.499732	0.0115784	intron-variant	DTX2	GRCh38.p7	7:76495983	CTCATCTCTCTGCCA[C/G]CCGCGCCCGCTTGTC	113878
rs113834200	snp	C/G			intron-variant	DTX2	GRCh38.p7	7:76499002	GGTGAGGTGTGTAGG[C/G]TGTGTAGAAGTGTGG	113878
rs113900068	snp	A/C			intron-variant	DTX2	GRCh38.p7	7:76491428	GAATAGCTGGGACTA[A/C]AGCTGTGTGCCAGCA	113878
rs114049378	snp	A/G	0.00199481	0.0315187	intron-variant	DTX2	GRCh38.p7	7:76495782	GGAGTCCAGCAGGGT[A/G]GGGCGGGAGGCTTGG	113878
rs114314090	snp	C/T	0.0260105	0.111035	intron-variant	DTX2	GRCh38.p7	7:76499354	TTAAACAAACCGTGC[C/T]GACTCCAGCCTCCAC	113878
rs114817577	snp	A/T	0.00874735	0.0655527	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76476748	TGGAACTTTCTAGAA[A/T]TAGATGTAGGTATCA	113878
rs114827474	snp	C/T	0.0170251	0.090679	intron-variant	DTX2	GRCh38.p7	7:76504685	GGTGGGGTCAGGAGC[C/T]CCTGAGAGTCAGAGT	113878
rs115954225	snp	C/T	0.021333	0.101051	intron-variant	DTX2	GRCh38.p7	7:76481155	CCCTCTGCATGTGTG[C/T]GTTTCTGCTTTTTGG	113878
rs116187285	snp	C/G	0.0295035	0.117819	intron-variant	DTX2	GRCh38.p7	7:76505167	ACTGAGGCGGGGTGG[C/G]CTGGAGCCCAGGTTC	113878
rs116423476	snp	A/G	0.00716266	0.059414	intron-variant	DTX2	GRCh38.p7	7:76495787	CCAGCAGGGTGGGGC[A/G]GGAGGCTTGGAGGGA	113878
rs116848658	snp	C/T	0.459861	0.135861	intron-variant	DTX2	GRCh38.p7	7:76483638	TGGCTGCAGGTGGCA[C/T]GGGTGACCTGGCCCC	113878
rs117127389	snp	A/G	0.00159617	0.0282053	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474561	TGAAGGATTAGTTGT[A/G]ACAGATTTCAGCAGG	113878
rs117218704	snp	A/G	0.0659589	0.169201	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76479907	TTCATGGGCCTGTGC[A/G]GCGGTACGTAGGCTG	113878
rs117327610	snp	C/G	0.0803336	0.186944	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505735	TGCCCCACCTGAAGC[C/G]GGGGCTCCCCCTGCC	113878
rs118035240	snp	A/G	0.152778	0.230321	intron-variant	DTX2	GRCh38.p7	7:76503048	GTCATGTGGCGCATC[A/G]GAGCCTGGCTCGGCC	113878
rs118124993	snp	C/T	0.0648419	0.167978	intron-variant	DTX2	GRCh38.p7	7:76502760	GGGCACCGCCTCCCC[C/T]TCGGCCACTTGTAAG	113878
rs137896500	snp	A/G/T	0.000335179	0.0129415	missense, intron-variant	DTX2	GRCh38.p7	7:76497388	CTGTGTGTCTTAGCC[A/G/T]CGCACCCCAGCCCAC	113878
rs138102519	snp	C/G/T	0.000198513	0.00996088	missense	DTX2	GRCh38.p7	7:76482759	TGCCGCAGCGTGCGG[C/G/T]GCCAAGCAGGGCCGC	113878
rs138132666	snp	A/T			intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76479251	GGAGAAGGTCTCGGG[A/T]GGTGGAGCTCGGGAT	113878
rs138141868	snp	C/T	0.00132646	0.025719	missense	DTX2	GRCh38.p7	7:76483012	CCGGGGCCCGGTCTG[C/T]GCCCAGGCTGAACAC	113878
rs138213538	snp	A/G	0.481932	0.0933148	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76479529	TCTTCAGGATGGTGG[A/G]TGCTAATAGGGAGGC	113878
rs138278579	snp	C/T			synonymous-codon	DTX2	GRCh38.p7	7:76505529	CGGCTATCCCGACCC[C/T]AACTACCTGCAGAAC	113878
rs138326422	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76491266	CTCCCAAAGTGCTGA[A/G]ATTATAGGCGTGAGC	113878
rs138408537	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76497008	CACCCAGGAGACCCC[A/G]TGCCCCGGGCGGCTT	113878
rs138409926	snp	A/G	0.00026469	0.0115011	synonymous-codon	DTX2	GRCh38.p7	7:76482803	CACCATCATCGCTCC[A/G]CCGGGCCACACAGGC	113878
rs138461485	snp	A/G	0.00119737	0.0244387	downstream-variant-500B	DTX2	GRCh38.p7	7:76506495	GGTGCAGTGGCTCAC[A/G]CCTCTAATCCTAGCA	113878
rs138592614	snp	C/T	0.000204043	0.0100985	synonymous-codon, intron-variant	DTX2	GRCh38.p7	7:76503584	CATTCCCCATGGTAT[C/T]CAGGTGAGGGGCCTT	113878
rs138608765	snp	A/G	0.000153988	0.00877327	utr-variant-5-prime, upstream-variant-2KB	DTX2	GRCh38.p7	7:76480508	CGGGACTCCTTGGGA[A/G]GATGGCCATGGCCCC	113878
rs138731251	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76477537	AGAAAGCAAGCTTGG[A/C]GAGCTTAGATACTTC	113878
rs138807459	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76484333	TGGGCAACAAAGAGC[A/G]AAACTCCATCTCGGG	113878
rs138819395	snp	A/G	0.0629771	0.165899	intron-variant	DTX2	GRCh38.p7	7:76468178	GGGCTTCCCAGGGGC[A/G]GGTGCTGTTGGCATG	113878
rs139338193	snp	G/T			intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76470661	CCAATCTCAGTCTGA[G/T]AAGAATTCTGCTGGA	113878
rs139355667	snp	A/G	9.54426e-05	0.0069074	synonymous-codon	DTX2	GRCh38.p7	7:76505451	CACCACGGGTGAGAC[A/G]GACACCGTGGTATGG	113878
rs139451476	snp	C/T	0.491263	0.0655142	intron-variant	DTX2	GRCh38.p7	7:76494579	TGCCCCCTTCCTCTG[C/T]TCTTGAGGCTGAAGG	113878
rs139607197	snp	G/T	0.0670745	0.170406	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76479873	TGGTGACTAGCACCC[G/T]GAATTTATGCTCTCT	113878
rs139768070	snp	A/G/T	0.000272623	0.0116723	synonymous-codon	DTX2	GRCh38.p7	7:76480590	GGAATGGCAGGACGG[A/G/T]CTGGGCACCTGGCAC	113878
rs139847148	snp	C/G	0.000153988	0.00877328	missense, downstream-variant-500B	DTX2	GRCh38.p7	7:76502316	TGCATCATCTGCATG[C/G]AGAAGCTGTCCACAG	113878
rs139870332	snp	A/G	0.00358779	0.0422022	intron-variant	DTX2	GRCh38.p7	7:76499800	CCTCCAGCTTCGTGC[A/G]CGTGTGCACAGACAG	113878
rs140016316	snp	A/G	0.00119737	0.0244387	intron-variant	DTX2	GRCh38.p7	7:76482009	AGCCCTGGAAACTAT[A/G]TGTTTCCAGGAGTGT	113878
rs140118064	snp	C/G/T	9.89078e-05	0.00703172	missense	DTX2	GRCh38.p7	7:76482924	TACCCCGTCCCCCAG[C/G/T]ACCCCCCACACAGGA	113878
rs140184005	snp	G/T			intron-variant	DTX2	GRCh38.p7	7:76485462	TCCGGGGCATCTTCT[G/T]CCAGGAGTTGGGGCA	113878
rs140372801	snp	C/T	0.0825414	0.185628	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474148	CTGGTCTCAAACTCC[C/T]GACCTCAGGTGATCC	113878
rs140389019	snp	A/T			intron-variant	DTX2	GRCh38.p7	7:76504677	CCCTGCCGGGTGGGG[A/T]CAGGAGCTCCTGAGA	113878
rs140413917	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76495030	GAGGCACTGCTTCCA[A/G]GTGACAGTGCCTCCA	113878
rs140991145	snp	C/G	0.00125102	0.0249789	missense	DTX2	GRCh38.p7	7:76505598	CTGCCTGGAGCAGCA[C/G]TGACCTCGCACCCCA	113878
rs141099391	snp	C/T	0.494526	0.0520291	intron-variant	DTX2	GRCh38.p7	7:76489624	GTCAGGAGTTTGAAA[C/T]CAGCCTGGCCAACAC	113878
rs141181111	snp	A/G	0.000104362	0.0072229	missense	DTX2	GRCh38.p7	7:76505408	TGGCCTGGAAGAGGC[A/G]GCTCATCTTCACAGT	113878
rs141299024	snp	A/C/T	0.00126984	0.0251705	missense, intron-variant	DTX2	GRCh38.p7	7:76497343	CCCGTGCAGGCATGA[A/C/T]GAGTGTTCTGATGTC	113878
rs141436878	snp	C/T	0.0134394	0.0808645	synonymous-codon	DTX2	GRCh38.p7	7:76482605	CGATGGCTCCTGGAC[C/T]GCCTATGAAGCCAGC	113878
rs141532437	snp	A/C	0.0948562	0.196037	intron-variant	DTX2	GRCh38.p7	7:76465038	TCACCTCCCAGGCTC[A/C]AGAGGTTCTTGTGCC	113878
rs141567991	snp	A/G	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76504744	AGACCAGGTGACCAC[A/G]GAAGGCTGGAGCAGT	113878
rs141587206	snp	C/T	0.207696	0.246395	synonymous-codon, downstream-variant-500B	DTX2	GRCh38.p7	7:76502327	CATGGAGAAGCTGTC[C/T]ACAGCGTCTGGATAC	113878
rs141623125	snp	A/G	0.000185756	0.00963553	missense, downstream-variant-500B	DTX2	GRCh38.p7	7:76502389	CCCTAGCTGTGGGCC[A/G]CCTCACCAAGTGCAG	113878
rs141629645	snp	A/T			intron-variant	DTX2	GRCh38.p7	7:76496802	GTATGGGGATGCTGC[A/T]GTGTGGGAGCAGGCC	113878
rs141720355	snp	G/T	0.215446	0.2476	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76476095	TTTTTTAAGACTGAT[G/T]TGTATTCCATCATTA	113878
rs141762993	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76490334	CGTCCCCTCACCCCC[C/T]CAAAAAAAGAAAATT	113878
rs141848345	snp	C/T	0.0948562	0.196037	intron-variant	DTX2	GRCh38.p7	7:76481956	TCCTGCCTTGGCCTC[C/T]GAAAGTGTTGGGATT	113878
rs142037291	in-del	-/AAA	0.488606	0.0746142	intron-variant	DTX2	GRCh38.p7	7:76463090	AAAAACAAACAAACT[-/AAA]AAAACGAACTTTTTT	113878
rs142063346	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76494941	GCCCGGCTGCGGAGA[C/T]GAGCGTTTGCGCACA	113878
rs142067417	snp	C/G	0.293551	0.246177	intron-variant	DTX2	GRCh38.p7	7:76499985	CCTGTACATGCTGGA[C/G]CCCAGACTCCCTTGT	113878
rs142130454	snp	C/T	3.41886e-05	0.00413438	synonymous-codon	DTX2	GRCh38.p7	7:76480677	CCAACGTTTTGGGCT[C/T]GGGAGCCTGGCCCAC	113878
rs142155908	snp	A/C/G	0.000104523	0.00722854	missense	DTX2	GRCh38.p7	7:76483081	GCCAGCCCCTCTACC[A/C/G]CTCCAGCCTCTCCCA	113878
rs142244705	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76503047	AGTCATGTGGCGCAT[C/T]GGAGCCTGGCTCGGC	113878
rs142279985	snp	A/G	0.00119737	0.0244387	downstream-variant-500B	DTX2	GRCh38.p7	7:76506493	CAGGTGCAGTGGCTC[A/G]CGCCTCTAATCCTAG	113878
rs142283581	snp	A/G			intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76480077	acttgggaaggctga[A/G]gcgagtctatccctt	113878
rs142391670	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76498804	TGTATGGGTGTGTGG[A/G]GGTGTGGGGTGTGTG	113878
rs142474507	snp	A/G	0.000397219	0.0140873	missense	DTX2	GRCh38.p7	7:76482999	AAACCCTCACTCTCC[A/G]GGGCCCGGTCTGCGC	113878
rs142505659	snp	C/T	0.0015985	0.0282258	synonymous-codon, intron-variant	DTX2	GRCh38.p7	7:76497413	GCCCACCAGCCCTCC[C/T]GCCTCCCGTCTGGCT	113878
rs142596194	snp	A/C	0.0287284	0.116357	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76480396	GATGTGCATTGGTAA[A/C]TGCTCATGTCTGTCC	113878
rs142622275	snp	A/T			intron-variant	DTX2	GRCh38.p7	7:76499011	TGTAGGGTGTGTAGA[A/T]GTGTGGGGTGTGTGA	113878
rs142622941	snp	G/T	0.0836354	0.186609	intron-variant	DTX2	GRCh38.p7	7:76466836	CTCCTGACCTCAGGT[G/T]ATCCACCTGCCTCGG	113878
rs142812861	snp	C/T	0.030278	0.119257	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474163	CGACCTCAGGTGATC[C/T]GTGCCTGGCCTACTT	113878
rs142909384	snp	C/T	0.0941369	0.195465	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76480301	GAGAGTGAGACCCTG[C/T]AACCAAAAAAAAAAA	113878
rs142956876	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76485311	TTGGCCTCAAGCAAT[C/T]CTCTTGCCCCAGCCT	113878
rs143114796	snp	A/G	0.000479348	0.015474	splice-acceptor-variant	DTX2	GRCh38.p7	7:76492151	GCTCTTTTCTCCCCC[A/G]GTGCCTCCCTCCCCA	113878
rs143157862	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76490182	AATACATAAATTAGC[C/T]GGGTGTGGTGGCACG	113878
rs143259796	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76497750	TGATTTTTGTAAGCA[A/G]CAAGTTGTGGGTGAG	113878
rs143281708	snp	A/G	0.0178098	0.0926698	intron-variant	DTX2	GRCh38.p7	7:76464859	AGTCTAGTTGAAGAG[A/G]TAAAGTGAACATAGA	113878
rs143367620	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505780	CCTCCCCTCTGGGAA[C/T]TGGGCAGCCCTGGGC	113878
rs143601393	snp	C/T	8.3729e-05	0.00646973	synonymous-codon, intron-variant	DTX2	GRCh38.p7	7:76503551	CGAGGACTGCGGGAC[C/T]ATCCTCATAGTTTAC	113878
rs143637084	snp	A/G	4.99239e-05	0.00499594	synonymous-codon	DTX2	GRCh38.p7	7:76482719	CTACACCACCCACAC[A/G]CAGACCAACAAGACT	113878
rs143688035	snp	C/T	0.000337524	0.0129865	synonymous-codon	DTX2	GRCh38.p7	7:76480620	CCCCTACAGTGCCAC[C/T]GTCTGCAGCTTCATC	113878
rs143749495	in-del	-/AG			intron-variant	DTX2	GRCh38.p7	7:76504111	GGTGGGAAGATAACG[-/AG]GGGCAGCAGGCAGCG	113878
rs143776913	snp	A/C	0.00203217	0.0318112	synonymous-codon	DTX2	GRCh38.p7	7:76482794	CCCGGTGACCACCAT[A/C]ATCGCTCCGCCGGGC	113878
rs143934697	snp	C/G	3.29761e-05	0.00406041	missense	DTX2	GRCh38.p7	7:76482926	CCCCGTCCCCCAGCA[C/G]CCCCCACACAGGACC	113878
rs144058012	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76503232	TCCCTTAACGAAAAT[A/G]GCATGAGTTGCTGGT	113878
rs144382908	snp	C/T	0.000141423	0.00840782	stop-gained	DTX2	GRCh38.p7	7:76505593	GAGGACTGCCTGGAG[C/T]AGCAGTGACCTCGCA	113878
rs144402741	snp	C/T	0.0158469	0.0875917	intron-variant	DTX2	GRCh38.p7	7:76499488	GCAGCCCCTGAAGGC[C/T]GTGAGCTTGGATTCA	113878
rs144508207	snp	A/G	0.0134995	0.0811632	intron-variant	DTX2	GRCh38.p7	7:76466981	TCACGGATCACTGCC[A/G]CCCCAAATTCCTGGG	113878
rs144733078	in-del	-/C/CC/CCC/CCCC			downstream-variant-500B	DTX2	GRCh38.p7	7:76506049	TTGTGTGTGTGTGTG[-/C/CC/CCC/CCCC]CCCCCCCCCACTTCC	113878
rs144760720	snp	C/T	0.000418329	0.0144565	missense, downstream-variant-500B	DTX2	GRCh38.p7	7:76502329	TGGAGAAGCTGTCCA[C/T]AGCGTCTGGATACAG	113878
rs144789597	snp	G/T			intron-variant	DTX2	GRCh38.p7	7:76498805	GTATGGGTGTGTGGA[G/T]GTGTGGGGTGTGTGG	113878
rs144849274	snp	G/T	0.494484	0.0522255	intron-variant	DTX2	GRCh38.p7	7:76489640	CAGCCTGGCCAACAC[G/T]GTGAAACCCCTGTCT	113878
rs144914725	snp	C/T	0.0124508	0.0779125	synonymous-codon	DTX2	GRCh38.p7	7:76482902	CTCCATGACCAACCT[C/T]CCTGCATACCCCGTC	113878
rs145065555	in-del	-/TT			intron-variant	DTX2	GRCh38.p7	7:76469395	TACTGTGAATATTCC[-/TT]TTTTTTTTTTTTTTG	113878
rs145091528	snp	C/T			intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76472412	GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAG	113878
rs145151450	snp	A/G	0.00612774	0.055012	missense	DTX2	GRCh38.p7	7:76482982	CCTTTGCACCGTACA[A/G]CAAACCCTCACTCTC	113878
rs145254031	snp	A/G	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76505060	CCAGGGAGGGTGGGT[A/G]GGCGGGCGCTCGTCC	113878
rs145386505	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76466717	GATTCTCCTGCCTCA[A/G]ACTCCGGAGTAGCTA	113878
rs145491861	in-del	-/TTT			intron-variant	DTX2	GRCh38.p7	7:76486883	CTGCTGCTGCTGCTG[-/TTT]CTGCCCTTGCCTCTA	113878
rs145545137	snp	C/T	0.00088158	0.0209765	synonymous-codon, intron-variant	DTX2	GRCh38.p7	7:76503452	GCAGTGTCCCTCCTG[C/T]AAAACCATCTATGGA	113878
rs145648578	snp	A/T	0.464947	0.127663	intron-variant	DTX2	GRCh38.p7	7:76489667	GTCTCTACTAAAAAT[A/T]CAAAAATTAGCAGGG	113878
rs145964625	snp	A/C/T	0.363406	0.222853	missense, intron-variant	DTX2	GRCh38.p7	7:76497420	AGCCCTCCCGCCTCC[A/C/T]GTCTGGCTTCCAAAA	113878
rs146074154	snp	A/G	0.0209421	0.100162	intron-variant	DTX2	GRCh38.p7	7:76481980	TGGGATTACAGGCTC[A/G]AGCCGTCATGCCCAG	113878
rs146317679	in-del	-/TT			intron-variant	DTX2	GRCh38.p7	7:76463102	CTAAAAAAACGAACT[-/TT]TTTTTTTTTTTTTAA	113878
rs146431580	snp	A/G	0.499968	0.00399348	intron-variant	DTX2	GRCh38.p7	7:76489469	GCCCAGCATGCTTCC[A/G]GTGTGTCACTCTACC	113878
rs146537218	snp	A/G	0.000430442	0.0146641	synonymous-codon	DTX2	GRCh38.p7	7:76483001	ACCCTCACTCTCCGG[A/G]GCCCGGTCTGCGCCC	113878
rs146583498	snp	G/T	0.0652144	0.168387	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76475069	CCCAGCACTTTGGAA[G/T]GCCAAGGCAGGTAGA	113878
rs146593354	snp	A/C/G	4.9561e-05	0.00497775	missense	DTX2	GRCh38.p7	7:76482591	GAGTGGCTGAGCGAC[A/C/G]ATGGCTCCTGGACTG	113878
rs146616572	snp	G/T	0.197393	0.244402	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76472236	TACACTGGGATAGCA[G/T]CAGCCATTTAAAGTA	113878
rs146948125	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76468814	GTTGCCCAGGCTGGA[A/G]TACAGTGGCACAGTC	113878
rs146985587	snp	C/T	4.96225e-05	0.00498084	synonymous-codon	DTX2	GRCh38.p7	7:76482749	TTCCAGCTTCTGCCG[C/T]AGCGTGCGGCGCCAA	113878
rs146996594	in-del	-/G	0.4973	0.0366419	intron-variant	DTX2	GRCh38.p7	7:76498728	GGGCGACCCTGAGCT[-/G]GGGGCCATCGTTCTG	113878
rs147032778	snp	C/T	0.497329	0.0364438	intron-variant	DTX2	GRCh38.p7	7:76487975	CGAGCCCTCTGAGGA[C/T]GGTGAGGGCGATTGA	113878
rs147079258	in-del	-/TTTTTCTTTTTC			intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474182	CCTGGCCTACTTTTT[-/TTTTTCTTTTTC]TTTTTCTTTTTCTTT	113878
rs147150115	snp	A/G/T	8.43952e-05	0.00649548	missense	DTX2	GRCh38.p7	7:76480640	GCAGCTTCATCGAGC[A/G/T]GCAGTTTGTCCAGCA	113878
rs147213959	snp	C/T	0.000231535	0.010757	synonymous-codon	DTX2	GRCh38.p7	7:76482797	GGTGACCACCATCAT[C/T]GCTCCGCCGGGCCAC	113878
rs147393790	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474326	TCCCAAAACGCTGAG[A/G]TTACAGGTGTGAGCC	113878
rs147396948	snp	C/T	8.54197e-05	0.00653472	synonymous-codon	DTX2	GRCh38.p7	7:76480587	GTGGGAATGGCAGGA[C/T]GGGCTGGGCACCTGG	113878
rs147467766	snp	G/T			intron-variant	DTX2	GRCh38.p7	7:76485450	GAGTCAGAGTTTTCC[G/T]GGGCATCTTCTGCCA	113878
rs147644708	snp	A/G	0.0590772	0.161395	missense	DTX2	GRCh38.p7	7:76500441	ACTTCTCTCTTCTAG[A/G]AGCGACCCCGAAGCC	113878
rs147803309	in-del	-/AGCA	0.0096173	0.0686743	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505613	GTGACCTCGCACCCC[-/AGCA]CGCCCGCCTCTGGTG	113878
rs147908269	snp	C/T	6.75026e-05	0.00580919	missense, downstream-variant-500B	DTX2	GRCh38.p7	7:76502388	TCCCTAGCTGTGGGC[C/T]ACCTCACCAAGTGCA	113878
rs148119060	snp	A/C	0.000153988	0.00877328	missense	DTX2	GRCh38.p7	7:76482729	CACACGCAGACCAAC[A/C]AGACTTCCAGCTTCT	113878
rs148274129	snp	A/T	0.0652144	0.168387	intron-variant	DTX2	GRCh38.p7	7:76481925	CTGGTCTTCAACTCC[A/T]GAGCTCAAGTGATCC	113878
rs148279131	snp	C/T	0.0408906	0.137015	synonymous-codon	DTX2	GRCh38.p7	7:76492192	AAGCAGCCCAGGGAG[C/T]GTCCCTGCCACTGTG	113878
rs148349044	snp	C/G	0.00676609	0.0577691	downstream-variant-500B	DTX2	GRCh38.p7	7:76506263	CCTGGGGTTGTGGTT[C/G]ACAAAATGCCATTCA	113878
rs148430404	snp	C/T	0.0015163	0.0274927	missense	DTX2	GRCh38.p7	7:76482882	GTGTCAGGCCGCTAC[C/T]GCCACTCCATGACCA	113878
rs148587797	snp	C/G	0.000686049	0.0185082	missense, downstream-variant-500B	DTX2	GRCh38.p7	7:76502332	AGAAGCTGTCCACAG[C/G]GTCTGGATACAGCGA	113878
rs148666668	in-del	-/T	0.499984	0.00279548	intron-variant	DTX2	GRCh38.p7	7:76466413	TAATCTTTTTTTTTT[-/T]AATTTTAAAAAACTT	113878
rs148924865	snp	C/T	1.66549e-05	0.00288568	synonymous-codon	DTX2	GRCh38.p7	7:76482698	GGGGTACAACTACAC[C/T]GTCAACTACACCACC	113878
rs148933215	snp	A/G			intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501839	CTGGTAAGCCCTTCA[A/G]AGGCACAGGTCCCGG	113878
rs148985152	in-del	-/TTTT			intron-variant	DTX2	GRCh38.p7	7:76490996	CTATGAGAACCTGCT[-/TTTT]TTTTTTTTTTTTTTT	113878
rs149301449	snp	A/G	0.00125161	0.0249847	synonymous-codon	DTX2	GRCh38.p7	7:76480560	GTACACCAGCCCCGC[A/G]GCTGTGGCCGTGTGG	113878
rs149336008	snp	C/T	0.480853	0.0959518	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76470243	ATCCAGCTCCTCGTA[C/T]AGTGCCTTCACCCGG	113878
rs149401871	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76493023	TCTGCCTCCCAGGTT[C/T]AAGCAATTCTCCTGC	113878
rs149515676	snp	A/T	0.0652144	0.168387	intron-variant	DTX2	GRCh38.p7	7:76481922	AGGCTGGTCTTCAAC[A/T]CCTGAGCTCAAGTGA	113878
rs149540302	snp	C/T	0.49999	0.00219646	intron-variant	DTX2	GRCh38.p7	7:76488550	GAATGCCTTCACTTA[C/T]GGAACCTTAGAGTTG	113878
rs149647142	snp	C/T	0.000386175	0.0138902	synonymous-codon	DTX2	GRCh38.p7	7:76505514	CAACATTACGGGCCA[C/T]GGCTATCCCGACCCC	113878
rs149663777	snp	C/T	0.00358779	0.0422022	intron-variant	DTX2	GRCh38.p7	7:76499801	CTCCAGCTTCGTGCA[C/T]GTGTGCACAGACAGC	113878
rs149711050	snp	C/G	0.00557542	0.0525036	intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501529	CGCCAGCAGGACCCC[C/G]AACTCACACACAGCC	113878
rs149983793	snp	C/T	0.000429241	0.0146436	missense	DTX2	GRCh38.p7	7:76482973	CCCACCAGGCCTTTG[C/T]ACCGTACAACAAACC	113878
rs150141824	snp	A/G	0.000309629	0.0124386	missense, downstream-variant-500B	DTX2	GRCh38.p7	7:76502445	CTGGCCATGTACTGC[A/G]ACGGCAATAAGGTGC	113878
rs150185502	snp	A/G	0.0103295	0.0711199	intron-variant	DTX2	GRCh38.p7	7:76468140	ATGTTATCAACGCCC[A/G]GTGTGGCTCTGGGGA	113878
rs150299899	snp	C/T	0.00270716	0.0366913	missense, intron-variant	DTX2	GRCh38.p7	7:76497364	TTCTGATGTCAGCCA[C/T]TGGACTCCCTGTGTG	113878
rs150348976	snp	C/T	0.45762	0.139261	intron-variant	DTX2	GRCh38.p7	7:76495368	GAGTGGGGGCTTCAC[C/T]CTTCAGGGCTCTGAC	113878
rs150414605	snp	A/G	0.214541	0.247473	intron-variant	DTX2	GRCh38.p7	7:76491053	CCAGGCTGGAGTGCA[A/G]TGGTGCAATCTCGGC	113878
rs150478839	snp	A/G	0.0836354	0.186609	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76476895	CATTGGGGAGGCTGC[A/G]TGCCTTCGTGGAAAG	113878
rs150633953	snp	G/T	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76484217	GGCATGGTGGCCAGC[G/T]CCTGTAATCCCAGCT	113878
rs150741596	snp	A/G/T	0.000100674	0.00709424	missense	DTX2	GRCh38.p7	7:76480766	GCTGGACCCAGTTCC[A/G/T]CCAGGACACCGGTAA	113878
rs150857694	snp	C/T	0.0161463	0.0883881	missense	DTX2	GRCh38.p7	7:76482514	TGAAAATAGGCACCA[C/T]GCGGGCTGTGCGGAG	113878
rs150873946	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76498072	AAGCGGGTGCTGGCC[C/T]TGCTTCCACCCCTGG	113878
rs151048323	snp	A/C/T	0.000134475	0.00819884	synonymous-codon, downstream-variant-500B	DTX2	GRCh38.p7	7:76502369	TGACAGCAAGGCAAT[A/C/T]GGGTCCCTAGCTGTG	113878
rs151280183	snp	G/T			intron-variant	DTX2	GRCh38.p7	7:76504092	GATCGTAGGGCCTGG[G/T]GCAGGGTGGGAAGAT	113878
rs151329883	snp	C/G/T	0.011929	0.0763043	synonymous-codon	DTX2	GRCh38.p7	7:76482929	CGTCCCCCAGCACCC[C/G/T]CCACACAGGACCGCT	113878
rs181002707	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76479409	CAATGCTTCAGGGCA[C/T]CTGGGAGACATGAGG	113878
rs181043779	snp	A/C/G	0.00212683	0.0325414	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502472	GTGCCCCCACTGGCC[A/C/G]AGGGCGGAGGCGGGT	113878
rs181424929	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76501047	ACCAATCAGACTCCT[A/G]TTGCGCTTCCATAGA	113878
rs181447664	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76503340	GGCCAGCCCATTCCC[A/G]GGGCCCTTTACCATC	113878
rs181493521	snp	C/T	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76466684	GCAACCTCCACCTCC[C/T]GGGTTCAAGCTACTC	113878
rs181503294	snp	A/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB, utr-variant-5-prime	DTX2, FDPSP2	GRCh38.p7	7:76476974	TGTGAGAGTTGGTTC[A/T]TCCGGGCCATGAGGA	113878
rs181888318	snp	C/T	0.00279162	0.0372561	intron-variant	DTX2	GRCh38.p7	7:76464833	GAGTGGTTTTGCCCT[C/T]AGTTGCTTATAGTCT	113878
rs181991981	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76502964	GCCGCGCCCAGACTG[A/G]CCCCCAGCTGCTCTC	113878
rs182057291	snp	C/T	0.00716266	0.059414	intron-variant	DTX2	GRCh38.p7	7:76468825	TGGAGTACAGTGGCA[C/T]AGTCTCGGCTCACTG	113878
rs182560727	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76498828	GTGTGTGGGGTGTGT[A/G]GAGGTGAGGGTGTGT	113878
rs182742366	snp	C/T	0.00279162	0.0372561	intron-variant	DTX2	GRCh38.p7	7:76494771	CTGTGTAGACTCCTG[C/T]CTCCCCCAATTCAAG	113878
rs182992343	snp	A/G	0.00119737	0.0244387	intron-variant	DTX2	GRCh38.p7	7:76504534	CTCTGCTTCTGCAGC[A/G]GAGGACAGAGGCTGA	113878
rs183022704	snp	A/T	0.00483621	0.0489358	utr-variant-5-prime, upstream-variant-2KB	DTX2	GRCh38.p7	7:76480482	GGGTCTGAAGCTGTT[A/T]GGGAAAGCAGCGGGA	113878
rs183146539	snp	A/G	0.00159617	0.0282053	intron-variant	DTX2	GRCh38.p7	7:76490197	TGGGTGTGGTGGCAC[A/G]CACCTGTAGTCCCAG	113878
rs183274510	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76504816	GAGAAGGTTGGGGAC[A/G]AGCCTTCCAGGAAGG	113878
rs183551286	snp	C/T			intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471822	CAGATTGCTCTTGGC[C/T]ACCCAGGAGCCAGTG	113878
rs184199441	snp	C/T	0.0952156	0.196321	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474082	ATGTGCCACCACGCC[C/T]GGCAAATTTTGTATT	113878
rs184250301	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502641	CCTAGGCCTGCCCTA[C/T]TCTTCTAGGTCTGCC	113878
rs184488408	snp	C/G			intron-variant	DTX2	GRCh38.p7	7:76464310	GCTGGGCTACTGTAA[C/G]TAGCTTAGTATGTAA	113878
rs184596432	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76501034	TGTAATGAACAGGAC[C/T]AATCAGACTCCTGTT	113878
rs184919488	snp	C/T	0.00676609	0.0577691	intron-variant	DTX2	GRCh38.p7	7:76464263	TGGGAGAGGAGTCAG[C/T]GTTTGCAAAGTCATG	113878
rs184990425	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76479906	CTTCATGGGCCTGTG[C/T]GGCGGTACGTAGGCT	113878
rs185120009	snp	A/G	0.00636936	0.0560724	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505989	AAATGCTCTATAGCC[A/G]AAGCCAGCAGGTCCT	113878
rs185331531	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76483441	GTGGCCTCTGCTTGC[A/G]GGCTGCATGGCGAGC	113878
rs185335562	snp	C/T	0.00199481	0.0315187	intron-variant	DTX2	GRCh38.p7	7:76466713	TCCCGATTCTCCTGC[C/T]TCAGACTCCGGAGTA	113878
rs185483425	snp	C/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76478254	TGATAAGATGGGGAC[C/T]CTGGCTTCTGGTGTG	113878
rs185596389	snp	A/G	0.434467	0.168736	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502280	TGGCGAGCATGACCC[A/G]TGTTTGGTCTCCTCC	113878
rs185727007	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76481880	TGTTTTTTGTAAAGA[C/T]TGGGTCTCCATTGCC	113878
rs186018731	snp	A/G	0.0209421	0.100162	intron-variant	DTX2	GRCh38.p7	7:76491188	GTTTTAGTAGAGACA[A/G]GATTTTGCCATCTTG	113878
rs186332222	snp	A/G	0.00279162	0.0372561	intron-variant	DTX2	GRCh38.p7	7:76503148	TCCGACTGCAAATGC[A/G]ATTCACCCGTGGAGA	113878
rs186751870	snp	C/T	0.00041609	0.0144178	intron-variant	DTX2	GRCh38.p7	7:76503413	CTCAGTGGGTTGCGT[C/T]TGCCTCTGTCAGGAT	113878
rs186911365	snp	A/G	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76466570	TTTTATCTTACATGT[A/G]TATTTCTTTGTTTCT	113878
rs186981766	snp	G/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474166	CCTCAGGTGATCCGT[G/T]CCTGGCCTACTTTTT	113878
rs187010008	snp	C/G	0.0138799	0.0821421	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76480327	AAAAAAAAATCAGCT[C/G]TGGAAAAGCATCACG	113878
rs187313909	snp	C/T	0.000399281	0.0141238	synonymous-codon	DTX2	GRCh38.p7	7:76480692	TGGGAGCCTGGCCCA[C/T]AGCATCCCCTTGGGC	113878
rs187428017	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501323	GAAAGGAGCCTGAAC[G/T]TCCTCCTCATGTGTC	113878
rs187546018	snp	C/T	0.000385443	0.0138771	missense	DTX2	GRCh38.p7	7:76505450	GCACCACGGGTGAGA[C/T]GGACACCGTGGTATG	113878
rs187665637	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76504699	CTCCTGAGAGTCAGA[A/G]TGTGACAGGCAGGGA	113878
rs187831133	snp	C/T	0.00676609	0.0577691	intron-variant	DTX2	GRCh38.p7	7:76495991	TCTGCCACCCGCGCC[C/T]GCTTGTCCTTCTCTC	113878
rs187946371	snp	C/T	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76469466	GGCATAATCTTGGCT[C/T]ACTGCAACCTCCACT	113878
rs188650862	snp	C/T	6.59391e-05	0.00574153	synonymous-codon	DTX2	GRCh38.p7	7:76482914	CCTCCCTGCATACCC[C/T]GTCCCCCAGCACCCC	113878
rs188746200	snp	G/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76472203	TGGTAAGTTGACAGG[G/T]CCTGATATTAGTGAA	113878
rs189225160	snp	A/T			intron-variant	DTX2	GRCh38.p7	7:76499484	CTCTGCAGCCCCTGA[A/T]GGCCGTGAGCTTGGA	113878
rs189446344	snp	C/T	0.0123036	0.0774623	intron-variant	DTX2	GRCh38.p7	7:76464801	TCATGCCAGCTTCTT[C/T]GTGGGGAGAGGCAGG	113878
rs189456784	snp	G/T			intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76478297	ACTACCCCAGCAAGG[G/T]TTCAGTGAGAAGGGT	113878
rs189491181	snp	C/T	0.00199481	0.0315187	intron-variant	DTX2	GRCh38.p7	7:76488156	CTACAGAACATTCTC[C/T]TGGTTCCTGCTCTCT	113878
rs189574022	snp	C/T	0.00159617	0.0282053	intron-variant	DTX2	GRCh38.p7	7:76504815	AGAGAAGGTTGGGGA[C/T]GAGCCTTCCAGGAAG	113878
rs189583450	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76502954	CACATGAAGAGCCGC[A/G]CCCAGACTGACCCCC	113878
rs189752116	snp	C/T	0.00119737	0.0244387	intron-variant	DTX2	GRCh38.p7	7:76466980	ATCACGGATCACTGC[C/T]GCCCCAAATTCCTGG	113878
rs190199563	snp	A/G	0.00119737	0.0244387	intron-variant	DTX2	GRCh38.p7	7:76482007	CCAGCCCTGGAAACT[A/G]TGTGTTTCCAGGAGT	113878
rs190310682	snp	C/T	0.00993419	0.0697739	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76475259	GAGGTTGCAGTGAGC[C/T]GAGATCACGCCATTG	113878
rs190403484	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76502930	GATCCTGGGCCCCAC[A/G]GCAGCCTACACATGA	113878
rs190531013	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76475042	CCAGGTGCAGTGGCT[C/T]ACGCCTGTAATCCCA	113878
rs190665875	snp	C/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76480195	CTATTGTCCCAGCTG[C/T]TCTGGAGGCTGAGTT	113878
rs190683513	snp	A/G	0.0352966	0.128072	intron-variant	DTX2	GRCh38.p7	7:76503291	TGGAAGCCAGTTTCC[A/G]GGCAGGAGGCTGCCA	113878
rs191150389	snp	C/T	0.00051813	0.0160872	intron-variant	DTX2	GRCh38.p7	7:76503623	CCCCACTCCTGGCCA[C/T]TCCTCTTCCCACCCC	113878
rs191309249	snp	C/T	0.00835141	0.0640778	intron-variant	DTX2	GRCh38.p7	7:76466660	GCAATGGCACGATCT[C/T]GGCTCACTGCAACCT	113878
rs191599863	snp	A/G	0.0162398	0.0886349	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474279	AGACTGGTCTCAAAC[A/G]CCTGGCCTCAAGTGG	113878
rs191733394	snp	A/G	0.0345262	0.126772	intron-variant	DTX2	GRCh38.p7	7:76481109	CTGTCCCACCACTCA[A/G]TGGCTGTGTGCCCTG	113878
rs191861142	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76480389	GGCTACTGATGTGCA[C/T]TGGTAACTGCTCATG	113878
rs191917906	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501811	CTTCTGCTGTCATGT[C/T]GGGCCTGTGCTGCTG	113878
rs192219767	snp	C/T	0.00874735	0.0655527	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471258	ACTCCACTTCCTGGG[C/T]TCACGCCATTCTCCT	113878
rs192277062	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505837	CAGCTACCTCAGTGC[A/G]CAGGGCCCGTCTGTC	113878
rs192290514	snp	C/T	4.96192e-05	0.00498067	missense	DTX2	GRCh38.p7	7:76482805	CCATCATCGCTCCGC[C/T]GGGCCACACAGGCGT	113878
rs192435820	snp	C/T	0.00517822	0.0506191	intron-variant	DTX2	GRCh38.p7	7:76500674	TTCATCTCCCAGCCT[C/T]CCGAGACCCACATCG	113878
rs193233487	snp	A/T	0.107694	0.205546	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76475183	GGGCTTGGTGGTGGG[A/T]GCCTGTAATCCCAGC	113878
rs199532626	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76464903	ACTTGCTAAGAGGGT[A/G]TTTTCTTTCATTCTT	113878
rs199547870	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76484659	GCCTCCCTGCTCACC[A/G]GCCCACCCCTGCCCA	113878
rs199598165	snp	A/G	9.89054e-05	0.00703157	missense	DTX2	GRCh38.p7	7:76482915	CTCCCTGCATACCCC[A/G]TCCCCCAGCACCCCC	113878
rs199716653	in-del	-/A	0.449091	0.151204	intron-variant	DTX2	GRCh38.p7	7:76491688	GTTTTCAGAGTCTTT[-/A]TTTTTTTTTTTTTGA	113878
rs199743411	snp	A/G	0.00128716	0.0253362	intron-variant	DTX2	GRCh38.p7	7:76483166	TCGTGGGCAACGGCC[A/G]CTCGTTTTGTCTGCC	113878
rs199752778	snp	A/G	0.000596186	0.0172551	missense	DTX2	GRCh38.p7	7:76480589	GGGAATGGCAGGACG[A/G]GCTGGGCACCTGGCA	113878
rs199765447	snp	C/T			intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471452	AGGTGTGAGCCACCG[C/T]GCCCAGCCTGGTTTC	113878
rs199785248	snp	C/G/T			intron-variant	DTX2	GRCh38.p7	7:76495959	AAACTGCACCTGTCC[C/G/T]TGTCCTCTCTCATCT	113878
rs199799760	in-del	-/C			intron-variant	DTX2	GRCh38.p7	7:76494572	AGCACCTGCCCCCTT[-/C]CCTCTGCTCTTGAGG	113878
rs199811851	snp	C/T	0.00642596	0.0563177	missense	DTX2	GRCh38.p7	7:76483083	CAGCCCCTCTACCGC[C/T]CCAGCCTCTCCCACC	113878
rs199903121	snp	C/T	0.0782233	0.181639	intron-variant	DTX2	GRCh38.p7	7:76497524	TTGCTAAGCCTCCTT[C/T]CGGCCTCGCTGCCTC	113878
rs199908903	snp	C/G	0.000152855	0.00874093	missense	DTX2	GRCh38.p7	7:76492184	GGTCCCTCAAGCAGC[C/G]CAGGGAGCGTCCCTG	113878
rs199923654	snp	A/C			upstream-variant-2KB	DTX2	GRCh38.p7	7:76460148	TTTTCTTCTTTCTTT[A/C]TTTTCTTTTCTTTTC	113878
rs199998408	snp	C/T	0.0948562	0.196037	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76477499	AACACTTAGGATACA[C/T]GTTGATAACTGCATT	113878
rs200024612	in-del	-/T	0.351853	0.228311	intron-variant	DTX2	GRCh38.p7	7:76464421	ATTTTAGGAGATTTC[-/T]ATGAGGGTCATTTTA	113878
rs200046885	snp	C/G			intron-variant	DTX2	GRCh38.p7	7:76498732	GACCCTGAGCTGGGG[C/G]CCATCGTTCTGGTCT	113878
rs200191073	snp	A/T			intron-variant	DTX2	GRCh38.p7	7:76466424	TAATCTTTTTTTTTT[A/T]ATTTTAAAAAACTTT	113878
rs200206920	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76481847	TGGGTTTTTTTTTTT[C/T]GTGTTTGTTTGTTTG	113878
rs200270057	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76483691	GAGTGCCTGGTAGAG[C/T]GCTCAGCTCCTTGAG	113878
rs200270179	snp	C/T	0.0232847	0.105357	intron-variant	DTX2	GRCh38.p7	7:76463349	TGCTTTTTGTTGTTT[C/T]TTCAACCATCTCCTT	113878
rs200339465	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76488896	GAGTGAGACTCCGAG[A/G]AAAAAAAAAAAAGTG	113878
rs200381241	in-del	-/TCGTG			intron-variant	DTX2	GRCh38.p7	7:76481846	ATGGGTTTTTTTTTT[-/TCGTG]TTTGTTTGTTTGTTT	113878
rs200382355	snp	C/G	0.00636936	0.0560724	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76478575	GCACCTCCGCACCTG[C/G]CTAACTTTTAAATTT	113878
rs200401428	in-del	-/T			intron-variant	DTX2	GRCh38.p7	7:76491684	ATTGTTTTCAGAGTC[-/T]TTTATTTTTTTTTTT	113878
rs200404371	in-del	-/AA			intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76475702	AAAATAAAAAAAAAG[-/AA]AAAAAATCCCATAAT	113878
rs200474916	snp	C/T	0.000100642	0.00709303	synonymous-codon, downstream-variant-500B	DTX2	GRCh38.p7	7:76502348	GTCTGGATACAGCGA[C/T]GTGACTGACAGCAAG	113878
rs200539611	snp	A/G	0.0103295	0.0711199	intron-variant	DTX2	GRCh38.p7	7:76469052	TTACAGGCGTGAGCT[A/G]CCGCATTCAGCCCCA	113878
rs200545789	snp	C/T			upstream-variant-2KB	DTX2	GRCh38.p7	7:76460441	ACTGCAAGCTCCGCC[C/T]CCCGGGTTCACGCCA	113878
rs200602962	snp	A/G	0.00755907	0.0610114	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76472682	ACTTTAGAAAATGTG[A/G]AAAGTTCAGATATAT	113878
rs200752892	in-del	-/GCCCGCCT	0.449853	0.150196	intron-variant, utr-variant-5-prime, upstream-variant-2KB	DTX2	GRCh38.p7	7:76477157	CCATTCCGCCCGCCC[-/GCCCGCCT]GCCCGCCCGAGGGCA	113878
rs200793617	snp	C/G			intron-variant	DTX2	GRCh38.p7	7:76467116	GTTGCCCAGGCTGGT[C/G]TTGAACTCCTGGGCT	113878
rs200814868	snp	G/T			intron-variant	DTX2	GRCh38.p7	7:76481204	CTTTTTTTTTTTTTT[G/T]GAGACGGAGTCTGGC	113878
rs200872991	in-del	-/TAAA			intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76477801	GTGAGACTCGGACTC[-/TAAA]TAAATAAATAAATAA	113878
rs200874572	snp	C/T	0.000102323	0.00715199	synonymous-codon	DTX2	GRCh38.p7	7:76505523	GGGCCACGGCTATCC[C/T]GACCCCAACTACCTG	113878
rs200877207	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76467853	GAGCTAGGAATTAAG[A/G]GATGAGTAAGTGGAC	113878
rs200877417	snp	A/T	0.202651	0.245475	intron-variant	DTX2	GRCh38.p7	7:76488559	CACTTATGGAACCTT[A/T]GAGTTGCAGAGACCA	113878
rs200915063	snp	C/G			intron-variant	DTX2	GRCh38.p7	7:76464369	GCTCTGAGCGAGGAG[C/G]GTTATGTGGGCCATG	113878
rs200956113	snp	G/T			intron-variant	DTX2	GRCh38.p7	7:76498831	TGTGGGGTGTGTAGA[G/T]GTGAGGGTGTGTGGG	113878
rs201072127	snp	A/T			upstream-variant-2KB	DTX2	GRCh38.p7	7:76460357	ATTATTATTATTATT[A/T]TTTTTTTTTTTTGAG	113878
rs201114672	in-del	-/C	0.0142736	0.0832652	intron-variant	DTX2	GRCh38.p7	7:76483429	GTTAAAGGCCTGTGG[-/C]CCTCTGCTTGCGGGC	113878
rs201148598	snp	C/T			intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474223	TTCTTTCTTTCTTTT[C/T]TTTTTTTTTTTTTAA	113878
rs201157714	snp	A/G	0.000342231	0.0130766	missense, downstream-variant-500B	DTX2	GRCh38.p7	7:76502367	ACTGACAGCAAGGCA[A/G]TCGGGTCCCTAGCTG	113878
rs201182215	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76481851	TTTTTTTTTTTCGTG[C/T]TTGTTTGTTTGTTTG	113878
rs201238884	snp	A/G	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76483969	GACTGAGGCAGGAGG[A/G]TTGCTGGAGACCAGG	113878
rs201287277	in-del	-/A			intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76472761	AGTTTAAAAAAAAAG[-/A]AAAAAAAAGGTCTTC	113878
rs201377237	snp	C/G	0.206336	0.246157	intron-variant	DTX2	GRCh38.p7	7:76489553	GTGGCCAGGTATGGT[C/G]TCTCATGCCTGTAAT	113878
rs201380110	snp	A/T			intron-variant	DTX2	GRCh38.p7	7:76468448	ATCTGGCCCACTGCC[A/T]TTTTTTTTTTTTTTT	113878
rs201396226	in-del	-/TA			intron-variant	DTX2	GRCh38.p7	7:76491687	TGTTTTCAGAGTCTT[-/TA]TTTTTTTTTTTTTGA	113878
rs201473481	snp	G/T			intron-variant	DTX2	GRCh38.p7	7:76481852	TTTTTTTTTTCGTGT[G/T]TGTTTGTTTGTTTGT	113878
rs201483863	snp	A/G			intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76475051	GTGGCTCACGCCTGT[A/G]ATCCCAGCACTTTGG	113878
rs201596835	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76485253	TTTTCAGTTTTACGT[A/G]GAGGCAAGGTCTTGC	113878
rs201672530	in-del	-/AAAG	0.0126979	0.078662	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76475004	TGTTAATACTAAAAA[-/AAAG]AAGAAAAAAAAAACT	113878
rs201699508	snp	A/C/T	0.00299551	0.0385847	intron-variant	DTX2	GRCh38.p7	7:76482469	CCCTGTATCTTGGGG[A/C/T]TGCTAGCAGACTAAC	113878
rs201730830	in-del	-/C			intron-variant	DTX2	GRCh38.p7	7:76489899	ATTAAAAAAAAAAAA[-/C]AACAACAACCTTTAT	113878
rs201802917	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76504036	CAGAGGAGACTCAGA[C/T]GGGCCCTAGCCCTTT	113878
rs201870580	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76481205	TTTTTTTTTTTTTTT[A/G]AGACGGAGTCTGGCT	113878
rs201879668	snp	G/T			upstream-variant-2KB	DTX2	GRCh38.p7	7:76460188	TTTTTTTTTTTTTTT[G/T]AGACAGATTCCCACT	113878
rs201931701	snp	C/G	0.00119737	0.0244387	intron-variant	DTX2	GRCh38.p7	7:76505340	CTCACTCTCCGTCCC[C/G]TCCTTCCTCTTCCCC	113878
rs202057776	snp	C/T			intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471589	GTTGGAGTGTAGTGG[C/T]ACGATCATAGCTCAC	113878
rs202109159	snp	A/T			upstream-variant-2KB	DTX2	GRCh38.p7	7:76461234	AGGAAAGAAAGAGAG[A/T]AAAAAAGAAAAGAAA	113878
rs202178115	snp	A/T			upstream-variant-2KB	DTX2	GRCh38.p7	7:76460360	ATTATTATTATTTTT[A/T]TTTTTTTTTGAGACG	113878
rs202208940	snp	A/G	0.0183765	0.0940775	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505606	AGCAGCAGTGACCTC[A/G]CACCCCAGCACGCCC	113878
rs202211419	snp	C/G			intron-variant	DTX2	GRCh38.p7	7:76500645	TGCCAGGGCCTTGCT[C/G]CAGCCCCTTTGGTTT	113878
rs202227195	snp	C/T			intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474000	GATCTCGGCTCACTG[C/T]AACCTCCACCTCCCG	113878
rs367647576	snp	C/T	0.0147051	0.0844766	missense	DTX2	GRCh38.p7	7:76504384	CCAATCCCGGAAAGC[C/T]GTTCACTGCCAGAGG	113878
rs367675268	snp	C/T	1.65389e-05	0.00287562	missense	DTX2	GRCh38.p7	7:76482781	CAGGGCCGCCTTACC[C/T]GGTGACCACCATCAT	113878
rs367843947	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76490385	AACTAAAGGTTTTTT[C/T]TTTCTTTCTTGATTT	113878
rs367864021	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76466627	GCAGAGTTTCACTCT[C/T]ATTGCCTAGGCTGGA	113878
rs367896423	snp	C/T	0.499759	0.0109798	intron-variant	DTX2	GRCh38.p7	7:76495969	TGTCCTTGTCCTCTC[C/T]CATCTCTCTGCCACC	113878
rs367959879	snp	C/T	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76476771	AGGTATCAAAGGTGG[C/T]GGGCTTGGTGTGAGT	113878
rs367968035	snp	C/T	0.0017479	0.029511	intron-variant	DTX2	GRCh38.p7	7:76497312	GTCTCTCCCTCTCTG[C/T]GTGTCTGCTCTCACA	113878
rs367986216	snp	A/G			intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76501928	GAGTCTCGCTCTGTC[A/G]CCCAGGCTGGAGTGC	113878
rs368054433	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76489157	AACAGTCAACAAACA[A/G]ACTCAAACAGGCCAT	113878
rs368235303	snp	C/T	4.97088e-05	0.00498517	synonymous-codon, intron-variant	DTX2	GRCh38.p7	7:76497374	AGCCATTGGACTCCC[C/T]GTGTGTCTTAGCCGC	113878
rs368267038	snp	C/G			intron-variant	DTX2	GRCh38.p7	7:76463838	ACTGTTGATTGCCAC[C/G]TGTCTCAAATAAATT	113878
rs368392380	snp	C/T	0.000133956	0.00818292	synonymous-codon, intron-variant	DTX2	GRCh38.p7	7:76503530	CCAGATGTCGCTCCC[C/T]GGCCACGAGGACTGC	113878
rs368488057	snp	C/T	4.99663e-05	0.00499806	synonymous-codon	DTX2	GRCh38.p7	7:76482681	GTGGACTTGGCCCCC[C/T]TGGGGTACAACTACA	113878
rs368500347	snp	A/G	8.25593e-05	0.0064244	missense	DTX2	GRCh38.p7	7:76482867	AGCAGAACTGGCCCC[A/G]TGTCAGGCCGCTACC	113878
rs368550154	snp	C/G	1.73357e-05	0.00294407	intron-variant	DTX2	GRCh38.p7	7:76503607	GGGGCCTTCTTGAGT[C/G]CCCCACTCCTGGCCA	113878
rs368555421	snp	G/T	0.407158	0.194426	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76477378	GGCAAGTGCTAGGGG[G/T]GAGGGGCCAGGAGAG	113878
rs368597411	snp	C/G	0.00137919	0.0262239	intron-variant	DTX2	GRCh38.p7	7:76503421	GTTGCGTCTGCCTCT[C/G]TCAGGATGGAAGTCT	113878
rs368603053	in-del	-/A			intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76475702	AAAATAAAAAAAAAG[-/A]AAAAAAATCCCATAA	113878
rs368665521	snp	A/G	3.90465e-05	0.00441834	synonymous-codon	DTX2	GRCh38.p7	7:76505430	CTTCACAGTGGGCAC[A/G]TCCAGCACCACGGGT	113878
rs368726061	snp	G/T			intron-variant	DTX2	GRCh38.p7	7:76481425	CTCCTGACCTCAGGT[G/T]ATCTGCCTGCCTCGG	113878
rs368803468	snp	A/G	0.000153988	0.00877328	missense	DTX2	GRCh38.p7	7:76480543	CCTTCCCTGGTGCAG[A/G]TGTACACCAGCCCCG	113878
rs368859519	snp	A/G	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501481	CACAGCCAGCACGCA[A/G]CTTGGATCATGGGAG	113878
rs368859945	snp	C/T			intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501783	TGCCCTGTCCGTCCT[C/T]CCCATTTGGTGGCTT	113878
rs368870644	snp	A/G			intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76478613	AGATGGGATCTCACT[A/G]TGTTGCCCAGGCTGG	113878
rs368965162	in-del	-/CCTG			intron-variant	DTX2	GRCh38.p7	7:76483484	AACACTGGGTCACTG[-/CCTG]TACACTGACTCCCGC	113878
rs368991320	snp	C/T	0.00155356	0.0278275	synonymous-codon	DTX2	GRCh38.p7	7:76482980	GGCCTTTGCACCGTA[C/T]AACAAACCCTCACTC	113878
rs369145620	snp	A/G	0.00119737	0.0244387	intron-variant	DTX2	GRCh38.p7	7:76484022	TGATCGCACCACTGC[A/G]CTTCAGCCCCCTAGG	113878
rs369153706	snp	C/T	0.0298908	0.118541	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502526	TGTCCCCTGCAGGGG[C/T]GGGAGGGTTCCGGGG	113878
rs369183807	snp	C/T	5.57476e-05	0.00527927	intron-variant	DTX2	GRCh38.p7	7:76497525	TGCTAAGCCTCCTTC[C/T]GGCCTCGCTGCCTCT	113878
rs369195858	snp	C/T	0.000671771	0.0183149	synonymous-codon, downstream-variant-500B	DTX2	GRCh38.p7	7:76502447	GGCCATGTACTGCAA[C/T]GGCAATAAGGTGCCC	113878
rs369196839	snp	A/G	0.0111196	0.0737302	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76475260	AGGTTGCAGTGAGCC[A/G]AGATCACGCCATTGC	113878
rs369263978	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76503923	GAGGGGCTGGAGAAG[C/T]GGGGCCACAGCAGGG	113878
rs369379953	snp	C/T	0.111576	0.20818	intron-variant	DTX2	GRCh38.p7	7:76462814	CTCATGCCTGTAATC[C/T]CAGCCCTTTGGGAGG	113878
rs369395261	snp	C/T	0.499824	0.00938333	intron-variant	DTX2	GRCh38.p7	7:76496011	GTCCTTCTCTCCACC[C/T]GACATTCAGTTCCCA	113878
rs369495187	snp	A/G	1.87352e-05	0.0030606	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502493	GGAGGCGGGTGGCCC[A/G]CCCCCACAGTCCTGA	113878
rs369497406	snp	C/T	0.107694	0.205546	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76475574	TGCCTGTAATCCCAA[C/T]TACTTGGGAGGCTGC	113878
rs369577858	snp	A/T	0.000591789	0.0171914	utr-variant-5-prime, upstream-variant-2KB	DTX2	GRCh38.p7	7:76480470	TCCAGGCCAGAGGGG[A/T]CTGAAGCTGTTTGGG	113878
rs369794491	snp	C/T	3.49498e-05	0.00418015	missense	DTX2	GRCh38.p7	7:76483110	CACCTGGGACCGCAG[C/T]ACCTGCCCCCAGGAT	113878
rs369802603	snp	C/G	0.000214279	0.0103486	missense	DTX2	GRCh38.p7	7:76482923	ATACCCCGTCCCCCA[C/G]CACCCCCCACACAGG	113878
rs369804097	in-del	-/TTTTTC			intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474181	CCTGGCCTACTTTTT[-/TTTTTC]TTTTTCTTTTTCTTT	113878
rs369939692	snp	A/G	0.00874735	0.0655527	intron-variant	DTX2	GRCh38.p7	7:76483410	GGGCCTCCACATGGA[A/G]CAGAGTTAAAGGCCT	113878
rs369940151	snp	A/G			intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76478746	CTTGGTTTCCTGTCC[A/G]TAAGTGGGAGAAATG	113878
rs369985387	snp	A/G	0.000207297	0.0101787	synonymous-codon	DTX2	GRCh38.p7	7:76505508	GGACCGCAACATTAC[A/G]GGCCACGGCTATCCC	113878
rs370007296	snp	A/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76476428	GCTCACCCCTCCTTT[A/G]GTGTTTCAGAGCCTC	113878
rs370023447	snp	C/G	0.00159617	0.0282053	intron-variant	DTX2	GRCh38.p7	7:76504607	TAGGTACAGGGAGGG[C/G]AGCCTGGACCTCACA	113878
rs370124494	snp	A/G			intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471352	ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT	113878
rs370219816	snp	C/T	0.000153988	0.00877328	synonymous-codon	DTX2	GRCh38.p7	7:76482701	GTACAACTACACTGT[C/T]AACTACACCACCCAC	113878
rs370235862	in-del	-/GCT			intron-variant	DTX2	GRCh38.p7	7:76486847	TTTCTGTTGTGGTGG[-/GCT]GCTGCTGCTGCTGCT	113878
rs370289441	snp	C/T	0.00323431	0.0400836	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505639	CTCTGGTGGCCACCC[C/T]GCTGCCCCATGGCTG	113878
rs370431095	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76473162	ATGTTTTAAACAAAA[C/T]TTCTAGTAAAGTAGA	113878
rs370586191	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76493214	ACAGGCATGAGCCAC[C/T]GTGCCTGGCCATTTT	113878
rs370718408	snp	C/T	0.00119737	0.0244387	intron-variant	DTX2	GRCh38.p7	7:76468841	AGTCTCGGCTCACTG[C/T]AGCCTCCGCCTCCTG	113878
rs370743551	snp	A/C/T	6.7216e-05	0.00579691	missense, intron-variant	DTX2	GRCh38.p7	7:76503475	TCTATGGAGAGAAGA[A/C/T]GGGGACCCAGCCCCA	113878
rs370774997	snp	C/T	9.99151e-05	0.00706736	synonymous-codon	DTX2	GRCh38.p7	7:76482554	CCCCCAGCACTCAGC[C/T]CCTGGCCGAGGTGTC	113878
rs370872905	snp	C/T	0.000562678	0.0167637	missense	DTX2	GRCh38.p7	7:76480765	AGCTGGACCCAGTTC[C/T]GCCAGGACACCGGTA	113878
rs371033766	in-del	-/GGTGTGTAG			intron-variant	DTX2	GRCh38.p7	7:76498992	TGTGTGGAGGGGTGA[-/GGTGTGTAG]GGTGTGTAGAAGTGT	113878
rs371035434	in-del	-/TT	0.0995058	0.199628	intron-variant	DTX2	GRCh38.p7	7:76466593	TTGTTTCTCTGTCTC[-/TT]TTTTTTTTTTCTTTG	113878
rs371090096	in-del	-/TT			intron-variant	DTX2	GRCh38.p7	7:76463101	ACTAAAAAAACGAAC[-/TT]TTTTTTTTTTTTTTA	113878
rs371236219	snp	C/T			intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501747	TGTAAGACCCCACGC[C/T]GAGGGCCTCCCCCAG	113878
rs371261404	snp	C/T	0.00174647	0.0294989	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502246	TCCAAGACTGGCCCA[C/T]GTCAGCCCAGCCCAC	113878
rs371466218	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76491060	GGAGTGCAGTGGTGC[A/G]ATCTCGGCTCACTGC	113878
rs371502989	snp	A/G			intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76477408	GGCAGGGAGGCCAAG[A/G]TGGGTTGACTCTCTG	113878
rs371517327	snp	G/T			utr-variant-3-prime	DTX2	GRCh38.p7	7:76505869	TCTGGGGGCTGCTTC[G/T]GGCCCGCGGTGCTCG	113878
rs371579923	snp	G/T			intron-variant	DTX2	GRCh38.p7	7:76484857	TCCTGAGCAGGCTGC[G/T]TGAGTGACTTCACTC	113878
rs371583169	in-del	-/C	0.449979	0.150028	intron-variant	DTX2	GRCh38.p7	7:76484379	AGATAAAATGAGGAA[-/C]CCCCCCAGGATTTCC	113878
rs371602656	in-del	-/TTT			intron-variant	DTX2	GRCh38.p7	7:76486884	TGCTGCTGCTGCTGC[-/TTT]TGCCCTTGCCTCTAA	113878
rs371714277	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	DTX2, FDPSP2	GRCh38.p7	7:76469703	CGGCCAAATATTCCA[A/G]TTTTTAAACATCAGC	113878
rs371728466	snp	C/T			intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76501951	TGGAGTGCAGTGGCA[C/T]AATCTCAGCTCTGCA	113878
rs371768271	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76464456	TTATTTTTTTGAGTT[A/G]GGGTCTGCTTCTGCT	113878
rs371801097	snp	A/G	0.0373696	0.131485	intron-variant	DTX2	GRCh38.p7	7:76500202	TCTTCTGCATCCTCC[A/G]TGGCTCCTGGGGCTG	113878
rs371833707	snp	C/T	5.10026e-05	0.00504962	missense	DTX2	GRCh38.p7	7:76480666	CAGCAGAAGGGCCAA[C/T]GTTTTGGGCTTGGGA	113878
rs371856720	snp	C/T	0.000128877	0.00802633	intron-variant	DTX2	GRCh38.p7	7:76503638	CTCCTCTTCCCACCC[C/T]GCCCACATCCCAGCA	113878
rs372062282	snp	A/G	0.00199481	0.0315187	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502527	GTCCCCTGCAGGGGC[A/G]GGAGGGTTCCGGGGG	113878
rs372225395	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76477766	GATTGCAGCCACTGC[A/T]CTCTAGCCTGGGTGA	113878
rs372226447	snp	A/C	0.000346275	0.0131536	synonymous-codon	DTX2	GRCh38.p7	7:76482884	GTCAGGCCGCTACCG[A/C]CACTCCATGACCAAC	113878
rs372228863	snp	A/G	8.37051e-05	0.00646881	missense, intron-variant	DTX2	GRCh38.p7	7:76503531	CAGATGTCGCTCCCC[A/G]GCCACGAGGACTGCG	113878
rs372256230	snp	C/T	0.000264638	0.0114999	missense	DTX2	GRCh38.p7	7:76482802	CCACCATCATCGCTC[C/T]GCCGGGCCACACAGG	113878
rs372298248	snp	A/G			synonymous-codon	DTX2	GRCh38.p7	7:76505574	GGCTGCCCAGGGGGT[A/G]ACCGAGGACTGCCTG	113878
rs372440890	snp	A/G	6.60022e-05	0.00574428	intron-variant	DTX2	GRCh38.p7	7:76497313	TCTCTCCCTCTCTGC[A/G]TGTCTGCTCTCACAC	113878
rs372453520	snp	C/T			intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76479439	GAGCTAGAACCTGTG[C/T]TGCAGTTCCCAGCTC	113878
rs372457239	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76498616	GGGCTGGGCAGAGGC[A/G]AGGCCCAGGCTCACC	113878
rs372516310	snp	G/T			intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471540	CTGTTATTTATTTTT[G/T]TTTAAAGAGACAGGG	113878
rs372688420	snp	C/T	0.000461893	0.0151899	missense	DTX2	GRCh38.p7	7:76482931	TCCCCCAGCACCCCC[C/T]ACACAGGACCGCTTC	113878
rs372791517	snp	G/T			intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471117	ACGAAATCCTGCTTT[G/T]CTTGGGCATAAATAT	113878
rs372806582	snp	A/G	0.00046754	0.0152824	intron-variant	DTX2	GRCh38.p7	7:76480799	CGCTGTCTGCCTCTC[A/G]CACATATCTGGGTGC	113878
rs372863887	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76499683	CACTACCTAGAGAAC[A/G]CCCCGGGCCGCGCCG	113878
rs372967799	snp	A/G	3.40472e-05	0.00412583	missense, intron-variant	DTX2	GRCh38.p7	7:76497414	CCCACCAGCCCTCCC[A/G]CCTCCCGTCTGGCTT	113878
rs372970386	snp	A/T			intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76475709	AAAAAAAGAAAAAAA[A/T]TCCCATAATTCTTTG	113878
rs373052232	snp	C/T	0.00232597	0.0340232	intron-variant	DTX2	GRCh38.p7	7:76483152	GGTGCAGTCAGGTAT[C/T]GTGGGCAACGGCCGC	113878
rs373052973	snp	C/G	0.000218412	0.0104479	missense	DTX2	GRCh38.p7	7:76505436	AGTGGGCACGTCCAG[C/G]ACCACGGGTGAGACG	113878
rs373066661	snp	C/T			intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76475916	CTGATACTACAGGCA[C/T]GCACCACCACAAATG	113878
rs373077713	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76503943	CCACAGCAGGGTGTG[C/T]GTCGAGGAACCTTGG	113878
rs373098370	in-del	-/GA			intron-variant	DTX2	GRCh38.p7	7:76498813	TGTGGAGGTGTGGGG[-/GA]TGTGTGGGGTGTGTA	113878
rs373138655	snp	G/T			intron-variant	DTX2	GRCh38.p7	7:76464316	CTACTGTAAGTAGCT[G/T]AGTATGTAATAGAGG	113878
rs373250889	snp	C/T	0.422158	0.181278	intron-variant	DTX2	GRCh38.p7	7:76490109	AAGGCAGGCGGATTA[C/T]GAAGTCGAGAGATCA	113878
rs373466186	snp	C/T	0.000628827	0.0177206	synonymous-codon	DTX2	GRCh38.p7	7:76482998	CAAACCCTCACTCTC[C/T]GGGGCCCGGTCTGCG	113878
rs373560779	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76501009	CTGCAGCCCTGTCCT[C/T]CTGACCTCCTGTAAT	113878
rs373642190	snp	C/T	3.30764e-05	0.00406659	missense	DTX2	GRCh38.p7	7:76482772	GGCGCCAAGCAGGGC[C/T]GCCTTACCCGGTGAC	113878
rs373645575	snp	A/C	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76503020	GGCAGAGTTTAGAGG[A/C]TTAGAGAACCGAGTC	113878
rs373665199	snp	A/G			intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76472210	TTGACAGGGCCTGAT[A/G]TTAGTGAAACTACAC	113878
rs373669106	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76502775	CTCGGCCACTTGTAA[A/G]CACCGCAGACACTGT	113878
rs373678060	in-del	-/G	0.320096	0.239972	intron-variant	DTX2	GRCh38.p7	7:76488894	AGAGTGAGACTCCGA[-/G]GAAAAAAAAAAAAAG	113878
rs373764063	snp	A/G			intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76476664	TCTGGAAGGATGGGC[A/G]TGTTTGCTTGGGGGC	113878
rs373777117	snp	A/G	0.000165986	0.00910855	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505648	CCACCCCGCTGCCCC[A/G]TGGCTGGCTGGGTGG	113878
rs373806641	in-del	-/A			upstream-variant-2KB	DTX2	GRCh38.p7	7:76460354	ATTATTATTATTATT[-/A]TTTTTTTTTTTTTTT	113878
rs373888603	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76505265	GAGTGGATGAGTCAC[C/T]TGGGAGGGGCTGGGA	113878
rs373937329	snp	C/T			intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76472171	GGGGGGATGTGTCTG[C/T]TGTCAGGGAGGTGCC	113878
rs373955567	snp	A/G			intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502545	AGGGTTCCGGGGGTG[A/G]CTGTAGGAATGGGCC	113878
rs374020583	snp	C/G			intron-variant	DTX2	GRCh38.p7	7:76466590	TCTTTGTTTCTCTGT[C/G]TCTTTTTTTTTTTTC	113878
rs374268771	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76466351	AATAAATGTAGTAAG[C/T]TCTGGCAATCTAGGC	113878
rs374422589	snp	C/T			intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501776	AGGATCCTGCCCTGT[C/T]CGTCCTCCCCATTTG	113878
rs374522089	snp	C/T	0.00146332	0.0270096	intron-variant	DTX2	GRCh38.p7	7:76483165	ATCGTGGGCAACGGC[C/T]GCTCGTTTTGTCTGC	113878
rs374530870	snp	G/T			intron-variant	DTX2	GRCh38.p7	7:76486842	GTGGCTTTCTGTTGT[G/T]GTGGGCTGCTGCTGC	113878
rs374557489	snp	C/T	0.000399281	0.0141238	missense	DTX2	GRCh38.p7	7:76482673	ACCAGCTCGTGGACT[C/T]GGCCCCCCTGGGGTA	113878
rs374755114	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76469221	TAGCCATAGGGAGTC[A/G]TGGTAGCTGTGGCCA	113878
rs374758181	snp	A/G	0.000181061	0.00951303	intron-variant	DTX2	GRCh38.p7	7:76483186	TTTTGTCTGCCCTGT[A/G]TTTCCGCTCTTAGCC	113878
rs374855456	snp	C/G	0.0024057	0.0345986	intron-variant	DTX2	GRCh38.p7	7:76505359	TTCCTCTTCCCCCTC[C/G]TCCTCCCCGGGCAGG	113878
rs374991250	snp	A/G			intron-variant, downstream-variant-500B	DTX2, FDPSP2	GRCh38.p7	7:76469784	GCCAGTTTGTCCGTC[A/G]TCAGTCTGTCTTGGT	113878
rs375003111	snp	C/T			upstream-variant-2KB	DTX2	GRCh38.p7	7:76460929	TCTGCCTCCCGGGTT[C/T]AAGCGATTCTCTTGC	113878
rs375026440	snp	C/T	0.0331398	0.124385	intron-variant	DTX2	GRCh38.p7	7:76504351	GGTGTCTGTTCCTCC[C/T]GCAGGGCCCTGAGCA	113878
rs375034710	snp	C/T			intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474298	GGCCTCAAGTGGTCC[C/T]CCCACCTTGGCCTCC	113878
rs375137481	snp	C/T	0.0146672	0.084371	intron-variant, downstream-variant-500B	DTX2, FDPSP2	GRCh38.p7	7:76469766	AGCAAAACACATCTA[C/T]AGGCCAGTTTGTCCG	113878
rs375142588	snp	C/T	0.0023933	0.0345097	intron-variant	DTX2	GRCh38.p7	7:76483300	TGGGTGCCGAGGTGC[C/T]GTGGCCATCCAGAGC	113878
rs375196799	in-del	-/CCGTTTCAC			intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501425	TCTGGTGTGACTGGG[-/CCGTTTCAC]CCGTTTCACCCCAGG	113878
rs375217866	snp	A/G	0.218151	0.247963	intron-variant	DTX2	GRCh38.p7	7:76480917	TGGTGGTGGGTGGGT[A/G]CAGTGAGTGGGAACA	113878
rs375224831	snp	A/G	0.0189856	0.0955633	intron-variant	DTX2	GRCh38.p7	7:76500686	CCTCCCGAGACCCAC[A/G]TCGTTATGGTCTGAG	113878
rs375259629	snp	C/G	1.67438e-05	0.00289338	missense, intron-variant	DTX2	GRCh38.p7	7:76503516	GAGGTATTACGGTTC[C/G]AGATGTCGCTCCCCG	113878
rs375549335	snp	C/T	0.000150657	0.00867788	synonymous-codon, intron-variant	DTX2	GRCh38.p7	7:76503536	GTCGCTCCCCGGCCA[C/T]GAGGACTGCGGGACC	113878
rs375711612	snp	A/G	0.0146672	0.084371	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76479915	CCTGTGCGGCGGTAC[A/G]TAGGCTGCGGGATTG	113878
rs375720500	snp	A/G	0.00398564	0.0444627	intron-variant	DTX2	GRCh38.p7	7:76499511	TGGATTCAAACCAGA[A/G]CCCCTTCTGGTCCTG	113878
rs375794680	snp	C/T	0.0066097	0.0571066	intron-variant	DTX2	GRCh38.p7	7:76497330	GTCTGCTCTCACACC[C/T]GTGCAGGCATGACGA	113878
rs375829293	snp	C/T			intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76475710	AAAAAAGAAAAAAAA[C/T]CCCATAATTCTTTGA	113878
rs375831438	snp	A/G	0.00159647	0.0282079	missense, intron-variant	DTX2	GRCh38.p7	7:76497421	GCCCTCCCGCCTCCC[A/G]TCTGGCTTCCAAAAG	113878
rs375844762	snp	C/G	0.000508345	0.0159347	intron-variant	DTX2	GRCh38.p7	7:76501243	CCCAGTACCCAGGGA[C/G]TCTTCACTTGTCTCT	113878
rs375909136	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76495499	CTCCTCCTCTCCAGG[C/T]TTCTGGGTTGAAACT	113878
rs376049821	snp	G/T			intron-variant	DTX2	GRCh38.p7	7:76464249	GGGGCACAGTCACCT[G/T]GGAGAGGAGTCAGCG	113878
rs376209701	snp	C/T	1.68091e-05	0.00289901	synonymous-codon, downstream-variant-500B	DTX2	GRCh38.p7	7:76502312	GGACTGCATCATCTG[C/T]ATGGAGAAGCTGTCC	113878
rs376289670	snp	A/G	0.000144652	0.00850346	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502478	CCACTGGCCCAGGGC[A/G]GAGGCGGGTGGCCCG	113878
rs376310305	snp	C/T	0.000163987	0.00905352	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505617	CCTCGCACCCCAGCA[C/T]GCCCGCCTCTGGTGG	113878
rs376375118	snp	A/G/T	3.322e-05	0.00407542	synonymous-codon, missense	DTX2	GRCh38.p7	7:76483019	CCGGTCTGCGCCCAG[A/G/T]CTGAACACCACCAAC	113878
rs376441256	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76504584	TGCTCTTTTCTGGGG[A/G]CCTGCTGTAGGTACA	113878
rs376443274	snp	C/G			intron-variant	DTX2	GRCh38.p7	7:76463401	AGACTGTTGTACCTC[C/G]TGCTCCACCCAGGCT	113878
rs376471639	snp	A/C/T	0.000535107	0.0163485	intron-variant	DTX2	GRCh38.p7	7:76483161	AGGTATCGTGGGCAA[A/C/T]GGCCGCTCGTTTTGT	113878
rs376547215	snp	A/G			intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474589	AGGTCTGCAGTGATC[A/G]GATGGGTTTCTCACA	113878
rs376553180	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76503359	CCCTTTACCATCTGA[C/T]GGTGGAGGTGACGGT	113878
rs376629505	snp	A/G	0.00159617	0.0282053	intron-variant	DTX2	GRCh38.p7	7:76483405	ATTAAGGGCCTCCAC[A/G]TGGAGCAGAGTTAAA	113878
rs376648361	snp	A/G			intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471622	CAACTTTGAACCCCT[A/G]GGCTCAAAGCAGTCC	113878
rs376653406	snp	C/T	0.000115467	0.00759737	synonymous-codon	DTX2	GRCh38.p7	7:76482941	CCCCCCACACAGGAC[C/T]GCTTCTGTGTTTGGG	113878
rs376786877	snp	C/T	8.54153e-05	0.00653455	synonymous-codon	DTX2	GRCh38.p7	7:76505469	CACCGTGGTATGGAA[C/T]GAGATCCACCACAAG	113878
rs376836387	snp	C/T			upstream-variant-2KB	DTX2	GRCh38.p7	7:76460173	CTTTTCTTTCTTTTT[C/T]TTTTTTTTTTTTTTG	113878
rs376852955	snp	A/G	7.28233e-05	0.00603377	intron-variant	DTX2	GRCh38.p7	7:76503411	AGCTCAGTGGGTTGC[A/G]TCTGCCTCTGTCAGG	113878
rs376871413	snp	C/T	0.499759	0.0109798	intron-variant	DTX2	GRCh38.p7	7:76495963	TGCACCTGTCCTTGT[C/T]CTCTCTCATCTCTCT	113878
rs376890002	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76502779	GCCACTTGTAAGCAC[C/T]GCAGACACTGTCTCC	113878
rs376942434	snp	C/T	1.70388e-05	0.00291875	missense, intron-variant	DTX2	GRCh38.p7	7:76503447	AGTCTGCAGTGTCCC[C/T]CCTGCAAAACCATCT	113878
rs377120126	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76481943	GCTCAAGTGATCCTC[C/T]TGCCTTGGCCTCCGA	113878
rs377172273	snp	C/T	0.000153988	0.00877328	synonymous-codon	DTX2	GRCh38.p7	7:76480527	GGCCATGGCCCCAAG[C/T]CCTTCCCTGGTGCAG	113878
rs377182749	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76499056	TGTGTGGAGGTGGGT[A/G]TGTGGAGCTGTGTGT	113878
rs377390517	snp	A/G	0.179105	0.239737	intron-variant	DTX2	GRCh38.p7	7:76503944	CACAGCAGGGTGTGC[A/G]TCGAGGAACCTTGGG	113878
rs377413711	snp	A/G	3.45214e-05	0.00415446	missense	DTX2	GRCh38.p7	7:76482517	AAATAGGCACCATGC[A/G]GGCTGTGCGGAGACA	113878
rs377446110	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76488482	CAGTGCCAAATTTCA[A/G]CTTTCTGGGCTCCAA	113878
rs377456527	snp	A/T	0.0146672	0.084371	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76479839	AGGGGAATTATCAGT[A/T]GCAAGAAAGAAGCTG	113878
rs377529609	in-del	-/GT			intron-variant	DTX2	GRCh38.p7	7:76499011	GTAGGGTGTGTAGAA[-/GT]GTGTGGGGTGTGTGA	113878
rs377646114	snp	C/G			intron-variant	DTX2	GRCh38.p7	7:76465179	AATTGGGCCATAAAA[C/G]GGTGGGTAAGGTGAG	113878
rs377676639	snp	G/T			intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501745	CTTGTAAGACCCCAC[G/T]CCGAGGGCCTCCCCC	113878
rs386714816	multinucleotide-polymorphism	AG/GT			intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474514	TTCTCTCGGGACGGC[AG/GT]AGGCAGGACAGCCAG	113878
rs397839838	snp	C/G			intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474918	TCGCCACAAATCTCT[C/G]TCCAGAGGATCGTGG	113878
rs527260554	in-del	-/C			intron-variant	DTX2	GRCh38.p7	7:76465499	GCTTAATCTTTTCTG[-/C]CCCCCCCATCTGAGA	113878
rs527437404	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	DTX2	GRCh38.p7	7:76460978	TGGGATTACAGGCAC[A/G]AGCCACCACGCCCGG	113878
rs527489407	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76472974	CCTCTTGATACATAT[A/G]TTACCAAATTGTTTT	113878
rs527633398	snp	C/G	0.0023933	0.0345097	intron-variant	DTX2	GRCh38.p7	7:76463779	TGGGGATTGGGGAGG[C/G]TGGAATTTGAGGTCT	113878
rs527680020	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501837	TGCTGGTAAGCCCTT[C/T]AGAGGCACAGGTCCC	113878
rs527723651	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	DTX2	GRCh38.p7	7:76506027	TGCATGCATGCGTGT[A/G]TGCGCACTTGTGTGT	113878
rs527741783	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76492071	CTCAGTGACTCCCAC[C/T]TGGCCATGACGCAGT	113878
rs527862065	snp	A/C	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474363	CTTGGCCTGTTTTAC[A/C]TGTTGACGGACAGCA	113878
rs527899297	snp	A/G	0	0	intron-variant	DTX2	GRCh38.p7	7:76493664	ATAGTGGCTGAGAGG[A/G]GACAGGCCTGGAGGT	113878
rs527900839	snp	C/G	0.00835141	0.0640778	intron-variant	DTX2	GRCh38.p7	7:76481385	AGAGACGGGGTTTTG[C/G]CACGTTGGCCAGGCT	113878
rs528022047	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474965	TGTAAAGGAAAAGCA[A/G]GGTTTGTTTTTCCTG	113878
rs528071117	snp	C/G	0.000470438	0.0153296	synonymous-codon, intron-variant	DTX2	GRCh38.p7	7:76503557	CTGCGGGACCATCCT[C/G]ATAGTTTACAGCATT	113878
rs528123625	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76503238	AACGAAAATGGCATG[A/G]GTTGCTGGTGCAAAA	113878
rs528249997	snp	C/T	0.00636936	0.0560724	intron-variant	DTX2	GRCh38.p7	7:76484013	AGTGAGCTGTGATCG[C/T]ACCACTGCACTTCAG	113878
rs528251769	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76477585	AGCCAGGCATGGTGG[C/T]GCGTGCCTGTAGTCT	113878
rs528304513	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76498376	GCCCAGGGCTCTGCA[C/T]GCCCTGCCCTTCCCC	113878
rs528377935	snp	C/T	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76490311	AGCCTGGTAATAGAG[C/T]GAGACTCCGTCCCCT	113878
rs528412254	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76478567	ATTGGCATGCACCTC[C/T]GCACCTGGCTAACTT	113878
rs528453859	snp	C/T	0.0252325	0.109451	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471200	GGAGTCTTGCTCTGT[C/T]GCCCAGGCTGGAGTG	113878
rs528481922	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	DTX2, FDPSP2	GRCh38.p7	7:76469832	TGGAAACAGATTTGG[G/T]TTTTCTCAGTCCCTG	113878
rs528623097	snp	A/G			intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502137	AGTGATCGGCCTCCT[A/G]GAGTGCTGGGATTAC	113878
rs528660943	snp	A/G	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76505090	CAGCAACGGCTGTGG[A/G]AGCAGGGAGGACTCG	113878
rs528742189	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76500739	TCCTGAGCAAAGCCC[C/T]TCCTCTCCCGGCCCT	113878
rs528880910	snp	C/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76498491	CTTGGTGGGTCGCCT[C/G]GCTGGCCCCTTCTGA	113878
rs528928988	snp	A/G	0.00119737	0.0244387	intron-variant	DTX2	GRCh38.p7	7:76504037	AGAGGAGACTCAGAC[A/G]GGCCCTAGCCCTTTC	113878
rs528959931	snp	A/C	0.0023933	0.0345097	intron-variant	DTX2	GRCh38.p7	7:76500052	TCAAATCGTGGTGCC[A/C]CAACGCCCCCTGGAG	113878
rs529070168	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76479673	GTAGTCCTAGCTACT[C/T]GGGAGGCTGAGGCAG	113878
rs529076011	snp	C/T	0.0178098	0.0926698	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76478658	GCTCAAACCACCCTC[C/T]TGTCGCAGCCTCCCT	113878
rs529109742	snp	A/G	0.00119737	0.0244387	intron-variant	DTX2	GRCh38.p7	7:76487921	GAAGGACACTTCAGG[A/G]GGCAGTTGGTGCCCC	113878
rs529197731	snp	C/T	0.00636936	0.0560724	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471281	ATTCTCCTGCCTCAG[C/T]CTCCCTAGTAGCCGG	113878
rs529258221	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471798	ACCTTCTGACTGGCT[A/G]CAGGTGGTCAGATTG	113878
rs529463012	snp	C/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76489855	AATGAGTGACTTGAA[C/G]ATAATCATTGTAGGG	113878
rs529463943	snp	A/C			downstream-variant-500B	DTX2	GRCh38.p7	7:76506362	CCAGGCATGGTGACG[A/C]ATGCCTGTTATCCCA	113878
rs529477895	snp	C/T	0.000637958	0.0178486	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505610	GCAGTGACCTCGCAC[C/T]CCAGCACGCCCGCCT	113878
rs529479820	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76500790	GCCATCCTGGGAGCA[A/G]GAATTCCAGAGACAA	113878
rs529551160	snp	G/T	0.00119737	0.0244387	intron-variant	DTX2	GRCh38.p7	7:76490854	AAATCCCCCCAAAAT[G/T]GTGTTGCATCCCTCC	113878
rs529552382	snp	G/T	0.0119091	0.0762411	intron-variant, downstream-variant-500B	DTX2, FDPSP2	GRCh38.p7	7:76469856	GTCCCTGGATATCCT[G/T]GGGCAAGCTGCATGT	113878
rs529614162	snp	C/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76466617	TTTCTTTGAGGCAGA[C/G]TTTCACTCTTATTGC	113878
rs529648883	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76475334	AAAACAAAAAAAACC[C/G]TTTGATCATTAAAAA	113878
rs529710593	snp	C/T	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76464921	TTCTTTCATTCTTTT[C/T]GTTGTTGTTGTTTTG	113878
rs529832992	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76503132	GCTGCAAGGCTGTCT[A/G]TCCGACTGCAAATGC	113878
rs529870617	snp	C/T	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76502762	GCACCGCCTCCCCCT[C/T]GGCCACTTGTAAGCA	113878
rs529899593	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76495429	AAGGCTGTGGCCCTC[C/T]GAGTTATTCAGGTGT	113878
rs529961720	snp	A/G	1.65762e-05	0.00287886	missense	DTX2	GRCh38.p7	7:76482651	GAGCAGCAGGTGGCC[A/G]GGGGCAACCAGCTCG	113878
rs530264209	snp	C/T	0.00318978	0.0398085	intron-variant	DTX2	GRCh38.p7	7:76467707	CTTGCCTTTAAGGAG[C/T]GTATGCATTCTCCAG	113878
rs530264221	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76477258	GCACCCACAGAGCTG[C/T]CAATTCCTGTGTTCG	113878
rs530435926	snp	A/G	0.00119737	0.0244387	intron-variant	DTX2	GRCh38.p7	7:76467229	AGCTATTGCTAGACC[A/G]TTTCCTGAATGTAGT	113878
rs530596747	snp	C/T	6.97764e-05	0.00590621	synonymous-codon, intron-variant	DTX2	GRCh38.p7	7:76497440	GGCTTCCAAAAGTCA[C/T]GGCTCAGTTAAGAGA	113878
rs530626548	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76491181	TTTTGTAGTTTTAGT[A/G]GAGACAGGATTTTGC	113878
rs530632058	snp	C/T	0.497211	0.037236	intron-variant	DTX2	GRCh38.p7	7:76496160	TCACCCTGCCCACCT[C/T]GGCTCTGCTGCCCAG	113878
rs530707991	snp	A/G/T	1.6498e-05	0.00287206	synonymous-codon	DTX2	GRCh38.p7	7:76482950	CAGGACCGCTTCTGT[A/G/T]TTTGGGACCCACCAG	113878
rs530750641	snp	C/T	3.34896e-05	0.0040919	missense, intron-variant	DTX2	GRCh38.p7	7:76503523	TACGGTTCCAGATGT[C/T]GCTCCCCGGCCACGA	113878
rs530899604	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76478290	AGACTGTACTACCCC[A/G]GCAAGGTTTCAGTGA	113878
rs530999889	snp	G/T	0.00318978	0.0398085	intron-variant	DTX2	GRCh38.p7	7:76504074	CTGTCTTGAGCCAAG[G/T]TGGATCGTAGGGCCT	113878
rs531186811	snp	A/G	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76498751	TCGTTCTGGTCTGGC[A/G]TTCTCGCCACCGTGA	113878
rs531191367	snp	C/T	0.0111196	0.0737302	intron-variant	DTX2	GRCh38.p7	7:76504626	CTGGACCTCACATAG[C/T]CTCGAGGGAGGAGGA	113878
rs531192630	snp	A/G	0.00398564	0.0444627	intron-variant	DTX2	GRCh38.p7	7:76481181	TTTGGTCTGCGATGT[A/G]TTTTGATCTTTTTTT	113878
rs531318941	snp	C/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76473043	TCTGTGTTGCCCAGG[C/G]TGGTCTTGACCTCCT	113878
rs531461685	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76461904	CGCGGGGTGGCGCGG[A/G]GAGCCGGAGCCTAGC	113878
rs531481765	snp	C/T	0.0115144	0.0749975	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474221	TTTTCTTTCTTTCTT[C/T]TCTTTTTTTTTTTTT	113878
rs531524837	snp	A/G	0.000798403	0.0199641	downstream-variant-500B	DTX2	GRCh38.p7	7:76506080	TGCATCAGAGCAAGA[A/G]GGGGTTCCATGGGCT	113878
rs531549537	snp	A/G	0.00557542	0.0525036	intron-variant	DTX2	GRCh38.p7	7:76464017	CCTTACTGGGTGCCA[A/G]ATAAGATCTCTGTCT	113878
rs531589045	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76501919	TCTGAGACGGAGTCT[C/T]GCTCTGTCACCCAGG	113878
rs531715240	snp	C/T	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76493909	TGAATTCATTTCGTC[C/T]TTAAATCACTGAGGT	113878
rs531795908	snp	A/G			intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76472016	TCACATGCTAGTTTC[A/G]TGCCATCTTCCAGTA	113878
rs531799179	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76494994	AACCAGGAGGTCATG[C/T]TTTGGAAGGACTGAG	113878
rs531871708	snp	A/G	0.00676609	0.0577691	intron-variant	DTX2	GRCh38.p7	7:76481957	CCTGCCTTGGCCTCC[A/G]AAAGTGTTGGGATTA	113878
rs532091892	snp	A/G	0.0146672	0.084371	intron-variant	DTX2	GRCh38.p7	7:76464222	GTGAAGGAGGAGTAG[A/G]ACTTAGAAAGTGGGG	113878
rs532138267	snp	A/G	0.00318978	0.0398085	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474316	CACCTTGGCCTCCCA[A/G]AACGCTGAGATTACA	113878
rs532258927	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502683	AAAGGAGGACCAGTG[C/T]GGCTGGTTCCCTCCA	113878
rs532326466	snp	A/G/T	0.000853322	0.0206384	missense, downstream-variant-500B	DTX2	GRCh38.p7	7:76502433	CTGCTGTGCCTCCTG[A/G/T]CCATGTACTGCAACG	113878
rs532528346	snp	C/T	1.65326e-05	0.00287507	synonymous-codon	DTX2	GRCh38.p7	7:76482620	TGCCTATGAAGCCAG[C/T]GTCTGTGACTATCTG	113878
rs532564531	snp	A/G	0.00279162	0.0372561	intron-variant	DTX2	GRCh38.p7	7:76467343	AATGGGTAGAAAATG[A/G]AATCTTTGGGAACTT	113878
rs532744614	snp	A/G	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76466735	TCCGGAGTAGCTAGG[A/G]TTACAGGCATGCGCC	113878
rs532924775	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76479744	GAGCCGAGATCACAC[A/G]CCTGGGTGACAAGAG	113878
rs532933568	snp	C/T	0.0850919	0.187897	intron-variant	DTX2	GRCh38.p7	7:76487960	AACGTTCTGCAGGTC[C/T]GAGCCCTCTGAGGAC	113878
rs532970520	snp	C/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76500120	CAGCCTCAGAAGCGC[C/G]GGGGTCGGTTCCTCA	113878
rs532985173	snp	C/T	0.0252325	0.109451	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471394	TCTCGATCTCCTGAC[C/T]TCGTGATCCGCCCGC	113878
rs533043116	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	DTX2	GRCh38.p7	7:76460438	CTCACTGCAAGCTCC[A/G]CCTCCCGGGTTCACG	113878
rs533114148	snp	C/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471845	AGCCAGTGGGTTCTT[C/G]GTTCTGGAGAAGCTG	113878
rs533154096	snp	A/C	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76480227	TGAGGATTGCTTGAG[A/C]CCAGGAGTTTGAGGC	113878
rs533329378	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76491982	ACCCCTCCTGAGTCT[C/T]TCTGAATTGCCCAGG	113878
rs533333806	snp	C/T	0.00835141	0.0640778	intron-variant	DTX2	GRCh38.p7	7:76469248	GCCACCCAGAGAGGA[C/T]GTTCCAGCCACCATT	113878
rs533349723	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505663	ATGGCTGGCTGGGTG[A/G]CCAGGCAGGAAGTGC	113878
rs533367376	snp	G/T	0.00119737	0.0244387	intron-variant	DTX2	GRCh38.p7	7:76491093	CCTCTGCTGCCCGAG[G/T]TTCAAGTGATTCTCC	113878
rs533420977	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501440	GCCGTTTCACCCCAG[A/G]CTCCTCCTCTCCAAG	113878
rs533482968	in-del	-/T	0.00119737	0.0244387	intron-variant	DTX2	GRCh38.p7	7:76464305	ACACAGCTGGGCTAC[-/T]GTAAGTAGCTTAGTA	113878
rs533569077	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76466490	ATCTAATCATTTCAT[C/T]TGAACTTGTTTTCTG	113878
rs533573438	snp	A/G	0.00438332	0.0466095	intron-variant, utr-variant-5-prime, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76470308	CCTTCAGGATCTGGT[A/G]CTGTTCTGGAGTGGC	113878
rs533764602	snp	A/T	0.0310518	0.120672	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471434	CCAAAGTGCTGGGAT[A/T]ACAGGTGTGAGCCAC	113878
rs533790316	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76479838	GAGGGGAATTATCAG[C/T]AGCAAGAAAGAAGCT	113878
rs533855917	snp	A/G	0.000851426	0.0206152	missense	DTX2	GRCh38.p7	7:76500518	AAAGTGCCCCCAGAT[A/G]AGGTTTGTGTCTTGG	113878
rs533915329	snp	C/G	0.00676609	0.0577691	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76472225	ATTAGTGAAACTACA[C/G]TGGGATAGCAGCAGC	113878
rs533930272	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	DTX2	GRCh38.p7	7:76480427	TGTTCACAGATCTGC[C/T]GGAGGCGCTGGGCAA	113878
rs533989738	snp	C/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76472530	CGGGATTTCACCATG[C/T]TGGCCAGGCTGGTCT	113878
rs533991492	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76479396	CCTTTTTGGTTAGCA[A/G]TGCTTCAGGGCACCT	113878
rs534069059	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76500945	TTTATTCTTAAAGAC[A/G]GGTGCACACTGTCGC	113878
rs534145280	snp	A/G	0.00318978	0.0398085	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76473972	TATTGCCCAGGCTGG[A/G]GTGCAATGGCGCGAT	113878
rs534206398	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505920	AGAGACTTCCCCAGC[C/T]TGGACGGGCGTGGGT	113878
rs534235924	snp	C/T	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76490146	TCCTGGGCAACATAG[C/T]GAAACCCCGTCTCTA	113878
rs534254041	snp	A/G	0.0471551	0.14613	intron-variant	DTX2	GRCh38.p7	7:76464264	GGGAGAGGAGTCAGC[A/G]TTTGCAAAGTCATGA	113878
rs534354999	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76495699	CTGGAGATGCAGCTA[C/T]GGGTGGGACCTCGTG	113878
rs534372550	snp	C/T	0.0275645	0.114116	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76476540	AACCAGGGAGTGCGG[C/T]TGTGTTTGCGTAAGT	113878
rs534395955	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76463388	AGTGGGTGGAGGAAG[A/G]CTGTTGTACCTCCTG	113878
rs534499939	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76467976	ACGGTTTGAGGGGCT[C/T]GGGCAGGGCATCCCG	113878
rs534528103	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-5-prime	DTX2, FDPSP2	GRCh38.p7	7:76476987	TCATCCGGGCCATGA[A/G]GACATGTTGGGACAT	113878
rs534608263	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76496889	CAGATCAGCCAGGAG[A/G]GGCATGGAGCACACA	113878
rs534726299	snp	A/C			intron-variant	DTX2	GRCh38.p7	7:76499450	GCAGGTGCAGTTGTG[A/C]GCCCTCAGGCTTAGA	113878
rs534962073	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76469249	CCACCCAGAGAGGAC[A/G]TTCCAGCCACCATTG	113878
rs534977445	in-del	-/T	0.00119737	0.0244387	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471734	ATCCACTGCTGCCCC[-/T]ATTACTCCCCTACTT	113878
rs535081216	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-5-prime	DTX2	GRCh38.p7	7:76477102	CTGATTTGTACCTCA[C/T]TGTGGTTACAGAAAC	113878
rs535092096	snp	C/T	0	0	intron-variant	DTX2	GRCh38.p7	7:76504125	CGGGGCAGCAGGCAG[C/T]GGGCACTGGCTGCCA	113878
rs535132278	snp	C/T	0.00159617	0.0282053	intron-variant	DTX2	GRCh38.p7	7:76504558	AGGCTGAGGCCGGGC[C/T]GAGTGTCTGCTGCTC	113878
rs535139642	snp	A/G	8.29607e-05	0.00643999	synonymous-codon	DTX2	GRCh38.p7	7:76483013	CGGGGCCCGGTCTGC[A/G]CCCAGGCTGAACACC	113878
rs535140415	snp	C/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76468101	GGGAGAGGGAGGCCA[C/G]GGCCTGATTCCCGGA	113878
rs535140461	snp	C/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76477748	GGGGCTGCAGTGAGT[C/G]GTGATTGCAGCCACT	113878
rs535225394	snp	C/T	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76484617	ATCATCTCCTTTCTC[C/T]GCACTGGCCCTGGTC	113878
rs535256607	snp	C/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76470074	AGAGCCTTCTCTCCC[C/T]GCCCTTGCAGTCTCT	113878
rs535291138	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76469431	GGATTCTCATTCTGT[C/T]GCCCAAGCTGGAGTG	113878
rs535294880	snp	A/G	0.0700422	0.173537	intron-variant, upstream-variant-2KB, utr-variant-5-prime	DTX2	GRCh38.p7	7:76479036	ATGCAGCTGTGAATG[A/G]AGCAGGCTTGGGGTT	113878
rs535332671	snp	C/T	0.0988009	0.199095	intron-variant	DTX2	GRCh38.p7	7:76503814	TGGCCCTCCACTCTT[C/T]CCTGAACCAAGGAAG	113878
rs535449530	snp	A/G	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76504717	TGACAGGCAGGGACC[A/G]GGGGCTGTGTTAGAC	113878
rs535469960	snp	C/T	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76497557	ACTCTTCTGCACAGA[C/T]CCTCTTCCTTCTCTC	113878
rs535510380	snp	G/T	0.000257433	0.0113424	intron-variant	DTX2	GRCh38.p7	7:76500325	TGGCCTCCCTGTCTG[G/T]GCCCCTCTCGCATTT	113878
rs535522754	in-del	-/C			intron-variant	DTX2	GRCh38.p7	7:76488410	ACCATGGGCTTAGAG[-/C]CCCTCTGGGCCAGTG	113878
rs535532833	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76484803	TAAGACACAGTGACA[A/G]CGCCTCCCGCTCATT	113878
rs535940192	in-del	-/G	0.00557542	0.0525036	intron-variant	DTX2	GRCh38.p7	7:76500211	TCCTCCATGGCTCCT[-/G]GGGCTGAGCCGGGTC	113878
rs535952614	snp	A/G	0.00119737	0.0244387	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502155	GTGCTGGGATTACAG[A/G]CCTGAGCCACTGCGC	113878
rs536023616	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76479887	CGGAATTTATGCTCT[C/G]TTTCTTCATGGGCCT	113878
rs536094248	snp	C/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76494726	TTCGGGAAGCTGGTT[C/G]AGGCCTAAGGAAATA	113878
rs536175339	snp	A/C	0.0023933	0.0345097	upstream-variant-2KB	DTX2	GRCh38.p7	7:76460933	CCTCCCGGGTTCAAG[A/C]GATTCTCTTGCCTCA	113878
rs536191481	snp	C/T	0.0154538	0.0865337	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471510	CTGTGTTCCTGGATG[C/T]GGGTTCCTGCTTGGC	113878
rs536270406	snp	A/G			intron-variant, upstream-variant-2KB, utr-variant-5-prime	DTX2, FDPSP2	GRCh38.p7	7:76476993	GGGCCATGAGGACAT[A/G]TTGGGACATACCCCG	113878
rs536318353	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76492314	CTTGGTGGGGAGGAA[A/G]TTGTGATGTGGGGCC	113878
rs536517697	snp	C/T	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76497253	GTCACATCCTTGGCC[C/T]GAGCAGGGTTTGTTG	113878
rs536638331	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76494801	GGCCCAGTGTTGGTA[C/T]CTACTGGGGGAGCAT	113878
rs536642580	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76502909	GCCAGGCCTTGAGGC[A/G]GGGCTGATCCTGGGC	113878
rs536649631	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76465257	GGTGGGGACAGACAC[A/G]CTGATGCACATGGGA	113878
rs536668060	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76476313	CAGAGACTGGTGCAC[C/T]GACACGCCACTGTAT	113878
rs536698217	snp	A/T	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76495590	ACTCATGCGGCCTCC[A/T]GGGGGCTGGTGGTGG	113878
rs536796170	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76504912	AGAGCTGGTTCTGAG[C/T]GCCCAGCGAAGCCAC	113878
rs536824161	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76476491	CAGCTCTGCCCTCAG[A/G]GAGTTTCTGTTTTGG	113878
rs536875818	snp	A/G	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76503004	GCCTTCAGGCGGGAT[A/G]GGCAGAGTTTAGAGG	113878
rs537113697	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76503371	TGACGGTGGAGGTGA[C/T]GGTCTTGGGTGTTCT	113878
rs537391929	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-5-prime	DTX2, FDPSP2	GRCh38.p7	7:76476945	CTGTATTTCCCAGGC[C/T]GTTTTTGCAGAGTTG	113878
rs537443812	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76467873	AGTAAGTGGACAAGT[A/G]CGATGGGCATTCTCA	113878
rs537635332	snp	A/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76497636	CCCGCTCGGCAGCAG[A/T]GGCGGCCCCTGGAAG	113878
rs537672092	snp	C/T	0.000115665	0.00760389	intron-variant	DTX2	GRCh38.p7	7:76497293	GCCGAAGGAGTCTTC[C/T]AATGTCTCTCCCTCT	113878
rs537677696	snp	C/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76503711	CTCAGGCCCCCAGGT[C/G]CCCTAAGGCCAGAGC	113878
rs537695240	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76483496	CTGCCTGTACACTGA[C/T]TCCCGCCTTGTGCCA	113878
rs537825729	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474093	CGCCCGGCAAATTTT[A/G]TATTTTTAGTAGAGA	113878
rs537826618	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76481478	AAGCATGAGCCACCG[C/T]GCCTGGACCTGCAGT	113878
rs538012697	snp	G/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76465108	CATGCCTGGCTGATT[G/T]AGAGGGTGTTTGCTT	113878
rs538028566	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501531	CCAGCAGGACCCCCA[A/G]CTCACACACAGCCCC	113878
rs538063748	snp	A/C	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76500993	GCGTGATCACAGCTC[A/C]CTGCAGCCCTGTCCT	113878
rs538074033	snp	A/C	0.00119737	0.0244387	intron-variant	DTX2	GRCh38.p7	7:76464332	AGTATGTAATAGAGG[A/C]GGCTGGAAAAGCAGG	113878
rs538251863	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76481048	AAGGGTTCCTTTGGC[C/T]GGCAGGCCGGCATGG	113878
rs538258625	snp	C/T	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76492115	TCGTTTCCAATAAGT[C/T]AGCGGTGTGCAGTAA	113878
rs538277903	snp	C/T	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76463168	CTATAATCCCAGCTA[C/T]TCGGGAAGCTGAGGC	113878
rs538320907	snp	C/T	0.00517822	0.0506191	downstream-variant-500B	DTX2	GRCh38.p7	7:76506104	ATGGGCTCATCGGCT[C/T]CCATTTGATAACTGA	113878
rs538484738	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502086	GAGATGGGGTTTTCC[C/T]GTGTTGGCCAGGCTG	113878
rs538531513	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	DTX2	GRCh38.p7	7:76506462	CAAGACCTCATCTCT[A/G]AAAAAAAAATTAGGC	113878
rs538636352	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76475133	CCAACATGGTGAAGC[C/T]GCGTCTCTACTAAAT	113878
rs538698245	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501584	GACCCCCGAGGGCGC[A/G]CCTCTCCCTGATCCT	113878
rs538736980	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505846	CAGTGCGCAGGGCCC[A/G]TCTGTCCTCTGGGGG	113878
rs538788782	snp	A/G	0.0287284	0.116357	intron-variant	DTX2	GRCh38.p7	7:76465224	TGGGTGGGATTCAGG[A/G]TGAAGCAGAGTCATG	113878
rs538792507	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76491276	GCTGAGATTATAGGC[A/G]TGAGCCACTGCACCC	113878
rs538891213	snp	C/T	0.00119737	0.0244387	intron-variant	DTX2	GRCh38.p7	7:76481559	CATCCCTTACTCTAA[C/T]CTGGTGGTTGTCACT	113878
rs539042366	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474581	ATTTCAGCAGGTCTG[C/T]AGTGATCAGATGGGT	113878
rs539042914	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	DTX2, FDPSP2	GRCh38.p7	7:76469525	AGCCTCCCGAGTAAC[G/T]GGGACTACAGGCGCT	113878
rs539079683	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76477938	AGAACAAACCCAGGT[C/T]GGGTCTGGCTCTAAG	113878
rs539268075	in-del	-/A			intron-variant	DTX2	GRCh38.p7	7:76483890	AGACCCCATCTCCAC[-/A]AAAAAAAATTTTTTT	113878
rs539308196	in-del	-/GTTT			intron-variant	DTX2	GRCh38.p7	7:76481866	TTTGTTTGTTTGTTT[-/GTTT]TTTGTAAAGACTGGG	113878
rs539330659	snp	A/C	3.91581e-05	0.00442465	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502500	GGTGGCCCGCCCCCA[A/C]AGTCCTGAGCTGTCC	113878
rs539355737	snp	A/G	0.000356824	0.0133523	intron-variant	DTX2	GRCh38.p7	7:76504494	GGCCCTGACCAGGCG[A/G]CAGGAGGCCAGGCGC	113878
rs539398384	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76478837	GTTGGACCCTGGACC[A/G]GCACTCCAACAGCCG	113878
rs539438288	snp	A/G	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76488453	CTGCATAGCCCATTT[A/G]TTTTGTAGACTTGCA	113878
rs539441803	snp	C/T	0.00119737	0.0244387	intron-variant	DTX2	GRCh38.p7	7:76500890	GTGGCTGTCCTGCCC[C/T]CCGGCTATTGGGAGA	113878
rs539457177	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76484450	GACTGTCTGGGTGAC[C/T]TGGGGCTTCGTCATT	113878
rs539477008	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76500401	CCTCCTCTCCAGCCT[A/G]TGCTCCTCAGGACGC	113878
rs539503561	snp	C/G	0.00914312	0.0669923	intron-variant	DTX2	GRCh38.p7	7:76490056	TGGTTGGCTGGGCAC[C/G]GTGGCTCACTCCTGC	113878
rs539504901	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76479910	ATGGGCCTGTGCGGC[A/G]GTACGTAGGCTGCGG	113878
rs539560314	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76470210	GTCTTTCTCATACTG[C/T]AAGAACACGGCTGGC	113878
rs539683849	snp	A/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76504742	TTAGACCAGGTGACC[A/T]CGGAAGGCTGGAGCA	113878
rs539786012	snp	C/T	0.0829062	0.185956	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76473400	TAAGGACTTTAACGG[C/T]GGTGTGGGTTGAGTT	113878
rs539937490	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76498379	CAGGGCTCTGCACGC[C/T]CTGCCCTTCCCCTGC	113878
rs540230511	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471767	CCCTCTGGGTAGGCC[C/T]GTAAACCAGGGCTCC	113878
rs540266116	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471218	CCAGGCTGGAGTGCA[A/G]TGGCGCGATCTTGGC	113878
rs540351030	snp	A/G	0.0023933	0.0345097	intron-variant	DTX2	GRCh38.p7	7:76503947	AGCAGGGTGTGCGTC[A/G]AGGAACCTTGGGTTG	113878
rs540532750	snp	C/T	0.157311	0.232183	intron-variant	DTX2	GRCh38.p7	7:76487718	GATCTCCTTCCTCTC[C/T]GGCCTCCTGGCTTTG	113878
rs540659858	snp	A/G	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76482286	GATCGCTTGAGCCCA[A/G]GAGGTCAGGGTGGCA	113878
rs540666828	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76475288	TGCACTCCAGCCTGG[A/G]CAACAAGAATGAAAC	113878
rs540735799	snp	A/G	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76466279	ACAAGATTGATTAGT[A/G]CACACTCCTCAGTGT	113878
rs540906603	snp	C/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76501131	ATTTTAGCTGGGAGC[C/G]CTGGAGATACTGTTG	113878
rs541240888	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76467058	GGCACAGGCTACCAT[A/G]CTTAGCTAATTTTTA	113878
rs541424814	snp	C/G	0.00358779	0.0422022	intron-variant	DTX2	GRCh38.p7	7:76467143	GGCTCAAGCAATTCA[C/G]CCGCCTTGGCCTCCC	113878
rs541592800	snp	C/G			intron-variant	DTX2	GRCh38.p7	7:76482099	TGTGAAGTCAACTGA[C/G]AAAGATAGCAGACAG	113878
rs541640321	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76478087	ACACCCTCATTGTGA[A/C]AACACGCCCATGAAG	113878
rs541668836	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	DTX2, FDPSP2	GRCh38.p7	7:76469644	ATGATCTGCCTGCCT[C/T]GGCCTCCCAAAGTGC	113878
rs541726565	snp	A/G	1.67593e-05	0.00289471	missense, intron-variant	DTX2	GRCh38.p7	7:76503496	CCCAGCCCCAGGGAA[A/G]GATGGAGGTATTACG	113878
rs541848857	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76498079	TGCTGGCCCTGCTTC[C/T]ACCCCTGGGCTGTGG	113878
rs542071399	snp	A/G	0.0271762	0.113356	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76479262	CGGGAGGTGGAGCTC[A/G]GGATGTGGGGAAGAG	113878
rs542197031	snp	C/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76483808	CCTTTAATCCCAGCA[C/T]TTTGGGAGGCCAAGG	113878
rs542234006	snp	A/G	0.0821764	0.185298	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76477273	CCAATTCCTGTGTTC[A/G]GAGTTGTTGCAGGCC	113878
rs542253896	in-del	-/TTC	0.00199481	0.0315187	upstream-variant-2KB	DTX2	GRCh38.p7	7:76460816	TTTTCTTTTTCTTTT[-/TTC]TTCTTCTTCGTCTTT	113878
rs542259462	snp	A/G	0.0952156	0.196321	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76478231	CGTCCTCATAGTCGC[A/G]TGGCTTGTGATAAGA	113878
rs542306631	snp	G/T	0.00358779	0.0422022	intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501737	CTGTCTCCCTTGTAA[G/T]ACCCCACGCCGAGGG	113878
rs542368044	snp	A/T	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76491655	ATTTTCTTTATTCAC[A/T]ACAGGTATGAAATGA	113878
rs542387011	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76503179	TTTCTGCTCAGGATC[C/T]GAGTTTTCCCACTCG	113878
rs542417726	snp	C/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471024	AGGACCTCCTTGAGC[C/T]GGGCAGTAGCATCTC	113878
rs542521485	snp	C/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76464623	GCTGGTCTCTAACTC[C/G]TGGCCTCAAGGGATC	113878
rs542631398	snp	C/T			intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76479791	AGAAAAAAAAATACA[C/T]GCATGATGAAACACA	113878
rs542654584	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76490657	CTCCAGCCTGGGCTG[A/G]AGTACAGTGGTGAGA	113878
rs542718810	snp	A/C	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76481160	TGCATGTGTGCGTTT[A/C]TGCTTTTTGGTCTGC	113878
rs542783130	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76463887	TGCTTCTCCTGTTTA[A/G]CTAACTAGTCTTAGA	113878
rs542842869	snp	A/G	1.80315e-05	0.00300257	intron-variant	DTX2	GRCh38.p7	7:76482478	TTGGGGATGCTAGCA[A/G]ACTAACCTTTTGTTT	113878
rs542843293	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474627	AAGTTGAAAGTAGCC[A/G]TGGCTCAGTATGAGT	113878
rs542864220	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76475455	ACTTTGGGAGGCTGA[A/G]GCGGGTGGATCACTT	113878
rs542880031	snp	C/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474173	TGATCCGTGCCTGGC[C/T]TACTTTTTTTTTTCT	113878
rs543043086	snp	G/T	0.029116	0.117091	intron-variant	DTX2	GRCh38.p7	7:76481836	TTTTAAAAGTATGGG[G/T]TTTTTTTTTTCGTGT	113878
rs543044257	snp	A/G	0.0119091	0.0762411	intron-variant	DTX2	GRCh38.p7	7:76492422	CCCCAGAGTGAGCCC[A/G]GGTGCCCCTCCTTTT	113878
rs543073306	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76493692	GGTAGGGCGGCTGGT[A/G]CAGAGCCTGACCTCA	113878
rs543111051	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502538	GGGCGGGAGGGTTCC[A/G]GGGGTGGCTGTAGGA	113878
rs543279359	snp	A/C/G/T	0.000132338	0.00813353	missense	DTX2	GRCh38.p7	7:76482798	GTGACCACCATCATC[A/C/G/T]CTCCGCCGGGCCACA	113878
rs543433322	snp	A/T	0.000798403	0.0199641	intron-variant	DTX2	GRCh38.p7	7:76481203	TCTTTTTTTTTTTTT[A/T]TGAGACGGAGTCTGG	113878
rs543639562	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76465551	AGAGTTGGAGAAGCT[A/G]TTTGGGAGGGAGCAC	113878
rs543647384	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76476867	CCTAGGGCCTGGGCC[A/G]TGGTGCGCCCTCCAT	113878
rs543651729	snp	A/G	0.00159617	0.0282053	intron-variant	DTX2	GRCh38.p7	7:76464794	ACATACATCATGCCA[A/G]CTTCTTCGTGGGGAG	113878
rs543877689	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502620	TCTAAAGGCCTGGCC[A/G]GCTCTCCTAGGCCTG	113878
rs543900598	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76503045	CGAGTCATGTGGCGC[A/G]TCGGAGCCTGGCTCG	113878
rs544024397	snp	C/T	8.38104e-05	0.00647288	synonymous-codon	DTX2	GRCh38.p7	7:76483043	CACCAACGCCTGGGG[C/T]GCAGCTCCTCCTTCC	113878
rs544055337	snp	A/G	0.00993419	0.0697739	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471804	TGACTGGCTGCAGGT[A/G]GTCAGATTGCTCTTG	113878

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