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

DCAF8

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs531774679	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160250106	AGAATTAAAAGAATA[A/G]GCCAACTCAAAAAAG	50717
rs531899527	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160250927	TGGTCTGACAACTAC[C/T]TTACCTTGAGCCCGA	50717
rs531960121	snp	A/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160251681	ACATGTTGCCCAGGC[A/T]GGTCTCGAACTCCTG	50717
rs531982881	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160220250	CCAATGCCTGGAATA[A/G]TATCTATCTATAGTA	50717
rs532024442	snp	C/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160258940	CCTTCACCCGACATG[C/G]ATCTTCAGAGTTCAT	50717
rs532030416	snp	A/G	0.00159617	0.0282053	intron-variant	DCAF8	GRCh38.p7	1:160260275	CAAGGTCACATGGCT[A/G]AGAAATATTAGTCTA	50717
rs532053373	in-del	-/GAA	0.00279162	0.0372561	utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160215906	GAAAAGGGGCAGGAG[-/GAA]GAAGTATCTGGGAAT	50717
rs532146207	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160258972	AAAACACAAATGATA[C/T]AAATGCAATCTCAAC	50717
rs532164780	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160222997	TGCAGTCCTTTAGCA[A/G]CAGCCTTAGTCTCTC	50717
rs532169505	snp	A/G	0.00159617	0.0282053	intron-variant	DCAF8	GRCh38.p7	1:160252748	AAGGGATCAACATGA[A/G]AATCGTTGTAAAGGT	50717
rs532227103	snp	A/G	0.00159617	0.0282053	intron-variant	DCAF8	GRCh38.p7	1:160223903	TCCAGCCTGGACAAC[A/G]GAGTGAGATCCTGTC	50717
rs532252820	snp	A/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160230379	ATAGGCCAACTGGAT[A/T]GGGATGGATACAGCT	50717
rs532351636	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160216761	ACTTGCTTTTTAATA[A/T]ATTTATAGATATAAA	50717
rs532434802	snp	A/G	0.0178098	0.0926698	intron-variant	DCAF8	GRCh38.p7	1:160236432	TATATGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT	50717
rs532444310	snp	A/G	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160229750	AAATTGGCCAGGCAC[A/G]GTGGCTCATGCCTGC	50717
rs532508568	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160237279	AATATTAGAATTAGA[A/G]GTCATCTAGTTCATT	50717
rs532525358	snp	A/T	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160250791	AAGAATAGCAGAAAT[A/T]TAAGTAGCTCAAAGT	50717
rs532649794	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160257496	AAAAGCCTATTACTC[C/T]CCTGATAGAATACAA	50717
rs532759384	snp	C/T	0.00716266	0.059414	intron-variant	DCAF8	GRCh38.p7	1:160258002	CCAAAAGTGCTGGGA[C/T]TACAGCCATGAGCCA	50717
rs532763679	snp	A/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160234199	CCTCTGACAAGATCA[A/T]GCCACTGTACTCCAG	50717
rs532863172	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160240797	GCATAGCCATCTTCT[C/T]AGCGAAAGACGGAAA	50717
rs532926438	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160229938	TGAGGCAGGAGAATC[A/G]CTTGAACCCGGGAAG	50717
rs532980067	snp	G/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160233201	ACTTCAGCCTAGAAC[G/T]GTTCTAGGCAAAGTG	50717
rs533002802	snp	A/C	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160255003	GTTTGTACATAGTAG[A/C]CATTTATATTATTTT	50717
rs533060352	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DCAF8	GRCh38.p7	1:160262363	CCGCTTCCCGTCTTG[A/G]GTCATCCTTCTGCTA	50717
rs533261049	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160220639	GATCAAGCATCAAAG[C/T]GCTCTTGGGAGACTA	50717
rs533272808	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160232458	TCAGCCTGGACAACA[C/T]GGTGAAACCCCGTCT	50717
rs533275811	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160232011	GCCTGGCCAACATGG[C/T]GAGACCCCATCTCTA	50717
rs533304534	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160261631	TTTCAACGCTAAACC[A/G]TAACCAAACAACCTC	50717
rs533336928	snp	C/T	1.66535e-05	0.00288556	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239748	CAGTACTGGCTGCCG[C/T]CGTACCCAATCCCAC	50717
rs533376342	in-del	-/T	0.00159617	0.0282053	intron-variant	DCAF8	GRCh38.p7	1:160230644	AATTTCTAGTGCACG[-/T]TTATTTACATACGAA	50717
rs533542562	snp	A/G	1.6543e-05	0.00287597	intron-variant	DCAF8	GRCh38.p7	1:160231254	AGTATACAATGCATC[A/G]GTCTTACAAACTGTC	50717
rs533571248	snp	C/T	8.25198e-05	0.00642286	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160217637	GCCCTCCTCCTCGTC[C/T]GATGTGTCTGAGGAG	50717
rs533609755	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	DCAF8	GRCh38.p7	1:160239164	GATAAATGGCTGGTA[C/T]CAGTACAGTAGATGG	50717
rs533646425	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160227739	ATAAACAACATGTAA[A/G]GTAAGGCCATGGCTG	50717
rs533735836	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160222964	CCCAAAGAGCTCGCT[C/T]CTTAGGGCAGAGGAA	50717
rs533738466	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160232192	TCCAGCCTGCGCAAC[A/G]GAGCAAGACTGTCTC	50717
rs533759217	snp	A/C	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160253754	TCACTGGAGTCCCAG[A/C]GGTCGAGATTGCAGT	50717
rs533763924	snp	A/G	0.00119737	0.0244387	intron-variant	DCAF8	GRCh38.p7	1:160224110	ATTTTAAGCAATTCA[A/G]GACCACTGACTAAAG	50717
rs533800246	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160259650	GTTGATGAGGATCAC[C/T]GTATAGCCCAACAAG	50717
rs533803703	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160231584	ACAGGAAAAAAGCAC[A/G]TACATTTATTATATG	50717
rs533819069	snp	C/G	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160253075	ACCTAAGAAGGCTCT[C/G]GGAGAGGATGTTCAA	50717
rs533995898	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160225504	GACTTGAAAGTCCAA[A/G]CTCTTCCCACCATAC	50717
rs534056791	snp	A/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160226207	TATGGAGCTTTTTAC[A/T]TGTACATTACCTACC	50717
rs534153506	snp	A/C	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160237651	CCCACCTCAGCTGCC[A/C]AAGTAGCTGGGACTA	50717
rs534155410	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160229069	CTTTGAGAGGCCGAG[A/G]TGGGTGGATCACTTG	50717
rs534217747	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160244852	TCTCCCGAGTGATCC[A/G]CCCGCCTCGGCCTCC	50717
rs534327333	snp	C/T	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160256274	GAAGTCTGTTGCCAT[C/T]AACAGTTTTTGCCAT	50717
rs534507682	in-del	-/TTT	0.00438332	0.0466095	intron-variant	DCAF8	GRCh38.p7	1:160255617	TGGCTTTAATTATTG[-/TTT]TTTTATTTTTATTTT	50717
rs534562409	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160222344	CGCCCTGAACACTAA[C/T]GCTTTTTCATTTGGA	50717
rs534609703	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160233669	ACAAGGTCAAACAAA[C/T]ACAAAAGTTACCATG	50717
rs534618382	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	DCAF8	GRCh38.p7	1:160264261	AACAACTATTGAATT[C/G]CTGCTCTGGAAGGCC	50717
rs534811917	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160221592	ACCACTCTCTGAAAA[A/G]ACCTCATCAAGAGAT	50717
rs534913800	snp	G/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160241714	AAATTTTATCCGCCA[G/T]AAGTAAAAGCTGTCA	50717
rs535037710	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160247988	ACATACAAAAAAATT[A/G]ATCAGTTGGATTTAT	50717
rs535059901	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160218117	AAGATAGCATTACAC[A/G]TGGACGGCAATGGAC	50717
rs535094347	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160251769	CCACTGCACCTGGCC[A/G]TATAGTGTTTATTAA	50717
rs535103755	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160255215	GTATTCATGTTCTAC[A/G]AACTGCAGTAAGACA	50717
rs535108057	snp	A/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160247376	AAGAATAAAGCCTTA[A/T]ATTTTTAACCAATTA	50717
rs535169278	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	DCAF8	GRCh38.p7	1:160262577	GTCGCGCGAGCTCAC[G/T]GCTCGCAACCCTCCT	50717
rs535210422	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160250176	TGGCCTAAAAAGAGC[A/G]AATGCAGGCCGGCGC	50717
rs535239242	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160233592	GGAAAGAGAGGAGGA[A/G]CTGATGCTGCTCCTT	50717
rs535295564	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160232395	CGCCTGTAATCCCAG[C/T]ACTTTGGGAAGCCGA	50717
rs535438787	snp	G/T	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160247180	GCTGATGAGCTCACT[G/T]TCCCAGGTAGTTGGA	50717
rs535475353	snp	A/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160219048	CTCACCTTGAGCCAA[A/T]TAACTGCCCTTGATC	50717
rs535545038	in-del	-/AG	0.00358779	0.0422022	intron-variant	DCAF8	GRCh38.p7	1:160249886	TAAGTGCAATAATTC[-/AG]ACTCAAACAGCTATA	50717
rs535550586	in-del	-/GT			intron-variant	DCAF8	GRCh38.p7	1:160236314	TACATACATATATAC[-/GT]GTGTGTATATAAATA	50717
rs535858450	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160246618	GCAGAACTGTGAGAC[C/T]CTTGTCTCTATAAAT	50717
rs535891561	snp	A/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160243540	TGAGCCACCATGCCC[A/T]GCCATGTAATCTCTC	50717
rs535902396	snp	A/C	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160219596	TTGCCCTGAGCACAA[A/C]AGGCTCAGCTATAAG	50717
rs535927881	snp	C/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160223061	TCTAATCTCTTACCT[C/G]TCCCACCCTGAATCA	50717
rs535949900	snp	A/G	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160250327	AAATATTAGCCGGGC[A/G]TGGTAGTGCATGCCT	50717
rs535993015	snp	A/C	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160260819	CAGCATCACTCATCA[A/C]TCCCCAGCTTTTAGT	50717
rs536016690	snp	C/G			utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160216046	ATAGCAGCAAAAGCA[C/G]TTAAGGGCAAGAATT	50717
rs536081190	snp	C/T	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160258943	TCACCCGACATGGAT[C/T]TTCAGAGTTCATAAA	50717
rs536227680	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160242838	CTGCAATTTATAGTT[C/T]GCCAATCCTTGACCT	50717
rs536267141	snp	A/G	0.00279162	0.0372561	intron-variant	DCAF8	GRCh38.p7	1:160251028	AATCTCATGGTTTAT[A/G]TAATCCCAGCATTCT	50717
rs536337924	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160258239	GTAGTCCCAGCTACT[C/T]GAGAGGCTGAGATGG	50717
rs536503403	snp	G/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160217223	ACTGAATAGCCAGTT[G/T]TTCCCCCCACCCCTC	50717
rs536525043	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	DCAF8	GRCh38.p7	1:160264466	GTGTGCTCTTTTACA[C/T]AGGGGATTCAGAGAA	50717
rs536587484	snp	C/T	0.0115144	0.0749975	upstream-variant-2KB	DCAF8	GRCh38.p7	1:160263492	AAAAAAAAAAAAAAT[C/T]ACCCGGCATGGTGGA	50717
rs536595694	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160255325	TATTATCGTAGAGAC[A/G]GAGTCTCACTATCTT	50717
rs536617163	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160227100	TTCTGGAGGTTCACA[C/T]AATATTTGTACTTCA	50717
rs536617222	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160235914	CAGCTAATTTTTGTA[C/T]TTTTAGTAGAGGTGA	50717
rs536660508	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160249338	TTTAAATAACAAAAA[C/T]TTACTTTATTAAGTA	50717
rs536667359	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160236138	TGAATCTCTTAAACA[A/G]GAAGTATTTGTTTAT	50717
rs536676146	snp	C/T	0.00993419	0.0697739	intron-variant	DCAF8	GRCh38.p7	1:160235230	CCTCCACCTCCTGGG[C/T]TCAAGCGATTCTCCT	50717
rs536969499	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160221499	AAACCAGAAGAAAAT[C/T]TGAAATACCCTTTCA	50717
rs537002328	snp	C/T	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160256605	GGCACGTGAGGCAAA[C/T]ATGTATGCTTCACTT	50717
rs537068187	snp	A/G	0	0	intron-variant	DCAF8	GRCh38.p7	1:160257524	CAAGACTTAGAGCAC[A/G]AAACTCAAGATCCCA	50717
rs537204019	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160243821	TCCAAGGTGTTTCCT[A/G]TGTAGTTTCCTAAAC	50717
rs537262171	snp	C/T	0.0023933	0.0345097	intron-variant	DCAF8	GRCh38.p7	1:160255294	TTTTAATTTTTAAAA[C/T]AGATTTTTTTACTAT	50717
rs537311878	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160220797	TAACATTCTACGTTA[C/T]AATTACATTCTACTC	50717
rs537348162	snp	G/T	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160235201	TACAGTGGCATGATC[G/T]CAGCTCACTGCAACC	50717
rs537371812	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160226088	ATCCACATACTTCCC[A/C]TTTTAAGTGGCAATC	50717
rs537532321	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160248474	GGCGTGGAGGCTCAC[A/G]CCTGTAATCCCATCA	50717
rs537599644	snp	G/T	0.0023933	0.0345097	intron-variant	DCAF8	GRCh38.p7	1:160252846	CCAGAGAAAATCAAG[G/T]GACACAAATGAGAAG	50717
rs537604094	snp	A/T	0.0260105	0.111035	intron-variant	DCAF8	GRCh38.p7	1:160256029	TTTTTTTTTTTTTTT[A/T]TTTTTTTTTTTAAGA	50717
rs537820578	in-del	-/TATC	0.00318978	0.0398085	intron-variant	DCAF8	GRCh38.p7	1:160252270	TACAAGAGATAAAAG[-/TATC]TATCATTTTTTAAAA	50717
rs537828874	snp	G/T	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160217106	GCTGGGGGTGGGGGG[G/T]GAGCCAACTGTCATA	50717
rs538014891	snp	A/G	0.00119737	0.0244387	intron-variant	DCAF8	GRCh38.p7	1:160236452	TGTGTGTGTGTATAT[A/G]TATATATATCCTCAC	50717
rs538063046	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160252301	AAAAGATAAATAGAA[C/T]GCTGTTGTGGTTGAA	50717
rs538074260	snp	C/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160244418	ACTTCAGCATTGCCC[C/G]CTAGGCAAGAATCTT	50717
rs538076536	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160236255	ATTATGCTGAGGCAT[C/T]ACACACAAACACACA	50717
rs538185121	in-del	-/GTAGGT	0.00716266	0.059414	intron-variant	DCAF8	GRCh38.p7	1:160226862	ATATCCATTTGTTAA[-/GTAGGT]GTAGGTGTAAGTCTA	50717
rs538285534	in-del	-/A			intron-variant	DCAF8	GRCh38.p7	1:160219100	AAGGGAGGCCCACCC[-/A]ATCCTGAGCCTAAGC	50717
rs538310408	snp	A/C	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160221690	GTCATTCCTTAGAGG[A/C]CTTGGATAACCAGAC	50717
rs538340292	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160246674	CCCTAGGTGTCAAGT[A/G]TAGGAGCCACTGAAA	50717
rs538373589	snp	G/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160222401	CATCACTCAGGACAG[G/T]ACAGAGGTTCTTCCC	50717
rs538659607	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160244868	CCCGCCTCGGCCTCC[C/T]AAAGTGCTGGGATTA	50717
rs538723534	snp	G/T	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160244597	ACTCAGATGACTAAC[G/T]TCAAACCTATTATTA	50717
rs538723634	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160252129	GGCACCACCCAGTGG[C/T]CTATGTGTAAGCAAA	50717
rs538815868	snp	C/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160235346	ACCATGTTAGCCAGG[C/G]TGGTCTCGAACTCCT	50717
rs538872273	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160250104	TCAGAATTAAAAGAA[C/T]AGGCCAACTCAAAAA	50717
rs538885345	snp	A/C	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160242713	GCTCCACCACAACTA[A/C]TCAACTCCAGTATGT	50717
rs538926602	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160224142	GGGCTTTCCCTGACT[C/T]CCTAACAAGGCATTT	50717
rs539006674	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160228942	AAGTTGAGTGTAACC[C/T]AATGTCAGAGAAGAG	50717
rs539120520	snp	C/G/T	0.00358779	0.0422022	intron-variant	DCAF8	GRCh38.p7	1:160236074	AAAAAAATGGTGGGG[C/G/T]GGGGGTGACTGAGGG	50717
rs539129422	snp	A/C			missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239921	CATAGACAAAGCGGG[A/C]ACTTGAACCCAGCTC	50717
rs539156316	snp	C/G			utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160216311	AGAGTGTGTATGTAT[C/G]TGTGTGGTGTGTGTG	50717
rs539159301	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160232258	CAGGCACTGGCTCAT[A/G]CCTATAATCCCAGCA	50717
rs539184332	snp	C/T	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160243374	ATGTCCCACTCCTAG[C/T]TGGGTTGTAACTTCA	50717
rs539345189	snp	C/T	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160225272	CTGATGAAACATGAC[C/T]ACCTCAGGGGGTAGC	50717
rs539367103	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160216283	CAGCTAAAGGTAAGA[A/G]AGACAGAGTGAGAGA	50717
rs539404708	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160253870	AAGGAGGATAGTCCA[C/T]GCTTCCAAAAAAATA	50717
rs539462632	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160253217	GTTTCAAGGTGAGGA[C/T]AGGCTGGGCGCAGTG	50717
rs539466123	snp	A/T	0.00159617	0.0282053	intron-variant	DCAF8	GRCh38.p7	1:160260731	TTTTTTTTTTTTTTT[A/T]ACAAAAAATTTCCCA	50717
rs539475587	snp	G/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160226909	TGGTCTGCAGACACA[G/T]ATGTAAGTCATATAT	50717
rs539538292	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160223698	AGCCCAGGAGTTAGA[A/G]ACCAGCTTGGGCAAC	50717
rs539582342	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160231679	TAAACTAAAGGTATA[C/T]GAATGTACCATTCTT	50717
rs539741759	snp	G/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160238278	TAAACCACTAGCACC[G/T]TGAAACTGTCAAAAT	50717
rs540001660	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160259977	CACGTCTAAGCTGAC[C/T]AATTAAAAATCAGTT	50717
rs540063034	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160257276	ATCTGCTTTAAAAAA[A/C]AAAAAAGCTAATTCA	50717
rs540124401	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160229977	GCAGTGAGCCAAGAT[C/T]GTGTCACTGCACTCC	50717
rs540139096	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160245195	AGGGTATCTAACTCA[C/T]TTCCTTTTATGCCAC	50717
rs540139494	in-del	-/A			intron-variant	DCAF8	GRCh38.p7	1:160246141	AGCAAACTCCGTCTC[-/A]AAAAAAAAAAATTAA	50717
rs540176052	snp	C/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160223778	AGGCATGCACCTGTA[C/G]TCCCAGCTACTCACG	50717
rs540244842	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160251457	GCCTTCCACACTCTA[A/G]TAGCATAGTGGTTTT	50717
rs540295592	in-del	-/TTG	0.00716266	0.059414	intron-variant	DCAF8	GRCh38.p7	1:160231534	TTTGGAAAGAAAGAA[-/TTG]TTGTGTTTTCTCTGT	50717
rs540303605	snp	C/T			downstream-variant-500B	PEA15, DCAF8	GRCh38.p7	1:160215588	CAAGCACTGGAAATA[C/T]GGGTCTCCCAAAATG	50717
rs540319023	snp	A/G			upstream-variant-2KB	DCAF8	GRCh38.p7	1:160263633	ATGGAATGAGACTCC[A/G]TCTCAAAAAAAAAGT	50717
rs540490427	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160248848	GCAGTGAGCTATGAT[C/T]CTGCTACTCACTGCA	50717
rs540506163	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160237077	CATTACCAAGACATA[C/T]GGAATATGTTCAAGG	50717
rs540569404	snp	C/T	0.00478085	0.0486577	intron-variant	DCAF8	GRCh38.p7	1:160244762	AGCTGGGACTACAGG[C/T]GCCTGCCACCATGCC	50717
rs540636700	snp	A/G	0.00159617	0.0282053	intron-variant	DCAF8	GRCh38.p7	1:160248165	TACAAAAATTAGCCG[A/G]GCGTGGTGGCACATG	50717
rs540675075	snp	A/C	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160219346	AGGCTGGAAAAAACC[A/C]TCTCAGTGGCTTTCA	50717
rs540779983	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160252552	GATTAGTTAAGAAGT[A/G]TAATAAAAGCTTTGT	50717
rs540799023	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160220877	AGTAGTGCCTGGTAA[C/T]CCCCACTGCTGGAAA	50717
rs540864405	snp	A/C/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	DCAF8	GRCh38.p7	1:160262242	GGCTGGGAAGCGAGG[A/C/G]GGGGCGCAGGCCGAG	50717
rs540987346	snp	C/T	0.00318978	0.0398085	intron-variant	DCAF8	GRCh38.p7	1:160232467	ACAACACGGTGAAAC[C/T]CCGTCTCTACCAAAA	50717
rs541048611	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160260932	CAGGATGAACAGAAC[C/T]CAGGCAAACTAAGTT	50717
rs541048895	snp	A/C	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160231993	GCCAGGAATTTGAGA[A/C]CAGCCTGGCCAACAT	50717
rs541080105	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160241710	CTATAAATTTTATCC[A/G]CCAGAAGTAAAAGCT	50717
rs541085308	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160220261	AATAGTATCTATCTA[C/T]AGTAATGGACAACTT	50717
rs541088621	snp	A/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160219960	ACAACTTCTTTTAGT[A/T]CTCTCTGGACCAACC	50717
rs541109937	snp	C/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160258726	TTTGAGACCAGCCTA[C/G]GCAACAAAGTGAGAC	50717
rs541240992	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160232016	GCCAACATGGCGAGA[C/T]CCCATCTCTACTGAA	50717
rs541446137	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160244295	CTGAGTAACTGGCAG[C/T]GATTTTTCAGATGCG	50717
rs541468905	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160254734	AGGGGAAGGTTTCAG[C/T]GAGCCAAGTCATGCC	50717
rs541496686	snp	A/G	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160262085	CCCTGTGAACTGTGC[A/G]GCTGGCTCTTGGGGG	50717
rs541562145	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160261434	TTTATGAATACACTT[C/T]AGTATTTTTAGGCCT	50717
rs541665515	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160225727	TTGAAGAGCTGCAAT[C/T]TGATGTAGTGGCAGG	50717
rs541714038	snp	C/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160231726	AGCTGCAGTCCAACA[C/G]AGTAACAGCCAGTTA	50717
rs541716952	snp	A/C	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160260939	AACAGAACTCAGGCA[A/C]ACTAAGTTCCAGTTT	50717
rs541999551	snp	C/T	0.00119737	0.0244387	intron-variant	DCAF8	GRCh38.p7	1:160253329	AACATCAGGAGACCC[C/T]GTCTCTAGAAAAAAT	50717
rs542139795	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160218122	AGCATTACACATGGA[C/T]GGCAATGGACAAAAG	50717
rs542173335	snp	C/T	0.211212	0.246973	intron-variant	DCAF8	GRCh38.p7	1:160236281	ACACACACACATACA[C/T]ACACGTACGTATATA	50717
rs542365159	snp	A/G	0.00279162	0.0372561	intron-variant	DCAF8	GRCh38.p7	1:160234526	CTGCCAAAGTCATTC[A/G]CTCTATTCATTACTT	50717
rs542513663	snp	C/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160259400	TAGCTGGGCATGGTG[C/G]CGCATGCCTGTAATC	50717
rs542520210	snp	C/T	0.00119737	0.0244387	intron-variant	DCAF8	GRCh38.p7	1:160219560	AGAACCTTGCACATC[C/T]CAGGGGGAACATCCT	50717
rs542553523	in-del	-/CTAA			intron-variant	DCAF8	GRCh38.p7	1:160258419	TCTTAGCCTCCCACT[-/CTAA]CTAATCATCCTAGGA	50717
rs542736482	snp	C/T	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160231629	GGGGAAAAAAATATG[C/T]AGTGAAGTCACTTTC	50717
rs542752436	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160249509	CAGCTTCAGGAATTT[A/G]TACAAGAAAAAAGAG	50717
rs542855566	snp	G/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160257134	TAATCTAAAACTCAC[G/T]GGCTTTTGGCTCTAA	50717
rs542980271	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	DCAF8	GRCh38.p7	1:160263866	AGCCTTACTGTCACT[C/T]CAGTCAAAGCATGTC	50717
rs543193093	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160235294	ATGTGCCACCACACA[C/T]GGCTAATTTTTGTAT	50717
rs543203001	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160216425	CCTCTGGTTAGAAGA[G/T]CCATCCTTGGAACCC	50717
rs543249922	snp	C/T	0.00199481	0.0315187	intron-variant	DCAF8	GRCh38.p7	1:160219813	TCCCTAAGGGAAGGG[C/T]AGGGAAGTTCCTACC	50717
rs543257746	snp	C/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160255747	GCCTCAGCCTCCCAA[C/G]TAGCTGGGACTACAG	50717
rs543263492	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160232783	TGGTCTTGCCACTGT[A/G]CTTCTGCTTAGGTGA	50717
rs543289428	snp	A/C	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160248130	GGCCAACATGGTGAA[A/C]CCCCCGTCTCTACTA	50717
rs543315254	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	DCAF8	GRCh38.p7	1:160262939	CATTTTCCCCTGAGA[A/G]TCCCCATTTACGTAT	50717
rs543324960	snp	C/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160240679	TATAAAAGTGTGCCT[C/G]ATACATCTACCATTG	50717
rs543483944	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160248696	GACAGAGCAAGACTC[C/T]ATCTCAAAAAAAGAA	50717
rs543487467	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160225945	GCCTCATGGGTTCAA[C/G]CAATTCTCTTGCCTC	50717
rs543538869	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160219196	TCCTATGTATAGGTC[A/G]GGGGTGGCTTCATCC	50717
rs543542739	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160256464	GTAAGGTTAACAAAA[C/T]ATACCTGGTAATGTG	50717
rs543656003	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160240914	TCACGCCTGTAATCC[C/G]AGCACTTTGGGAGGC	50717
rs543795841	snp	C/T	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160221894	CTTCATTCCCTAACT[C/T]GATTCTCACTCTTCC	50717
rs543798188	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160254141	AGCCTGGCCAACATG[A/G]TGAAGCTCCGTCTCT	50717
rs544044389	snp	C/T	1.66424e-05	0.0028846	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239763	CCGTACCCAATCCCA[C/T]ACCACCACCTTCAGG	50717
rs544064274	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160221032	CTCATTTACTCTTAG[A/G]ACCACTAAAACTTAG	50717
rs544135623	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160216844	TTTCTTAAAAAAATA[A/T]CAGAAGAGGTAATAT	50717
rs544159196	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160251261	AGCAGCTGTTCAGGG[C/T]TGATCTCCATCCAAA	50717
rs544199303	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160217492	CTAAAGCAAAAAGTC[C/T]AAAGTGCGTTTCTGC	50717
rs544226234	in-del	-/T	0.00318978	0.0398085	intron-variant	DCAF8	GRCh38.p7	1:160251950	GGTAGGCTGGACAGA[-/T]TGAGCAGAAAGAAAC	50717
rs544345211	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160257358	TCTGGTTTGGATACC[A/G]TTATTTCTCTTTTAT	50717
rs544493765	snp	C/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160235413	CATGAGCCACTGCAC[C/G]TGACCAAGATTTGTT	50717
rs544497321	snp	A/G	0.000148374	0.00861191	intron-variant	DCAF8	GRCh38.p7	1:160244070	AACCAAAACAATTAG[A/G]AAACCACCTGGGAAA	50717
rs544531572	snp	C/T	1.65438e-05	0.00287605	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160225648	ATTCTCATCAATTTT[C/T]CTCTGGTCATAAATC	50717
rs544596951	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160257784	AGGCGCAATCTCAGC[A/G]CACTGCAGTGATCAC	50717
rs544641391	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160229245	AGGTTGCAGTGAGCC[A/G]AGATCGAGCCACTAC	50717
rs544692047	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160242169	AGAATCGCTTGAACC[C/T]GGGAGGTGGAGGCTG	50717
rs544702746	snp	G/T	0.00199481	0.0315187	intron-variant	DCAF8	GRCh38.p7	1:160236623	CAAACAAGATGTTGT[G/T]TTTTTTCTATGATAC	50717
rs544709190	snp	C/T	0.00398564	0.0444627	intron-variant	DCAF8	GRCh38.p7	1:160236617	TGGATCCAAACAAGA[C/T]GTTGTGTTTTTTCTA	50717
rs545014122	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160228652	AAAAGCATGTCTCCC[C/T]AGAGCTTCCCTTAAA	50717
rs545173338	snp	A/C	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160243787	AGATAAAATCAGAAG[A/C]AGCAAAAGCATAATA	50717
rs545238994	snp	A/G	0.00358779	0.0422022	intron-variant	DCAF8	GRCh38.p7	1:160250421	CGGTGAGCCAAGATC[A/G]CACCATTGCACTCCA	50717
rs545302190	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160249762	TCTTCAGCTGGGTCA[C/T]AGATAAACAAATTGT	50717
rs545328284	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160257296	AAGCTAATTCAATCT[C/T]AGAGACTTAAAAACT	50717
rs545341272	snp	C/T	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160248653	GGTTGCAGTGAGCTG[C/T]GATCGCGCCACTGCA	50717
rs545362805	snp	A/G	0.00358779	0.0422022	intron-variant	DCAF8	GRCh38.p7	1:160234091	TCAAACTTTTTTCCT[A/G]AGATGTTAGTCAATT	50717
rs545487774	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160261062	CACTTCTAGGCTTAA[A/G]TCATTTGGAGATACA	50717
rs545517247	snp	A/C	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160227209	GAAAGGAAGACACAC[A/C]CATGAACAACACTGA	50717
rs545671264	snp	C/T	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160242068	GCTAACATGGTGAAA[C/T]CCCCATTTCTACTAG	50717
rs545680925	snp	A/T	0.000399281	0.0141238	downstream-variant-500B	PEA15, DCAF8	GRCh38.p7	1:160215385	CAACTAACTGATTTT[A/T]AAATTTCTGTGAGTG	50717
rs545704691	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160231115	TCACCCCTCAGAGAC[C/T]GTTACATTAGAGAAC	50717
rs545744123	snp	A/G	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160246015	TGGTGGCACATGCCT[A/G]TAATCCCAGCTACTA	50717
rs545809052	snp	C/G	0.00119737	0.0244387	intron-variant	DCAF8	GRCh38.p7	1:160245363	AGTATAATTATGACC[C/G]CAGTCCTTGTACCCA	50717
rs545846865	snp	A/G	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160260355	TGTACTTTTCTCTTT[A/G]TATCTTACTGATACA	50717
rs546023738	snp	C/T	1.64827e-05	0.00287073	intron-variant	DCAF8	GRCh38.p7	1:160218295	AAAAGGGTCACTCCC[C/T]TGGGAATTCATTTCC	50717
rs546029664	in-del	-/AG	0.00676609	0.0577691	intron-variant	DCAF8	GRCh38.p7	1:160222374	AAAAGGTGCACGTCT[-/AG]AGATAAGTTACATCA	50717
rs546084559	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160219100	GAAGGGAGGCCCACC[C/T]ATCCTGAGCCTAAGC	50717
rs546444025	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	PEA15, DCAF8	GRCh38.p7	1:160215783	TGCATGGTTTTTAGC[C/T]CACCCTATCACCCCA	50717
rs546466043	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160222958	TATTCTCCCAAAGAG[C/T]TCGCTCCTTAGGGCA	50717
rs546505097	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160252876	GCTGGCAGGTGGGAT[A/G]AGAAATTATTCTGAA	50717
rs546615857	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160252090	AGTCTAGGCTACTCA[C/T]TTTTATACAAATCAC	50717
rs546746003	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160258244	CCCAGCTACTCGAGA[A/G]GCTGAGATGGGAGAA	50717
rs546786194	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160257472	TTTTAATAGTCACTT[C/T]ATGATTTTAAAAGCC	50717
rs546847788	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160256825	AATTTATCTGTATCA[C/T]AACACATTCCTGGGG	50717
rs546975253	snp	A/C	0.000399281	0.0141238	downstream-variant-500B	PEA15, DCAF8	GRCh38.p7	1:160215691	CATCCATTGTGAATA[A/C]ATGGACCACATACCA	50717
rs547090459	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160232217	TGTCTCAAAAAAAAA[A/G]AAGTCACTTAAAACC	50717
rs547130494	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160246950	GACGACAGAGCAAGA[C/T]ACAGTCTCCAAAAAA	50717
rs547230058	in-del	-/A	0.00279162	0.0372561	intron-variant	DCAF8	GRCh38.p7	1:160246155	TCAAAAAAAAAAATT[-/A]AAAAAAACTTATAAA	50717
rs547233674	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160252980	AAGGCCAGAGATACA[C/G]ACTTGTGAATTATCT	50717
rs547366535	snp	C/G	0.00119737	0.0244387	intron-variant	DCAF8	GRCh38.p7	1:160224134	ACTAAAGAGGGCTTT[C/G]CCTGACTCCCTAACA	50717
rs547470753	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160231224	TTCGTAACTCTCCAT[A/G]AAGGAGCACCTGGTA	50717
rs547489875	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160259806	AACAGAGAGTCCAAG[A/G]TGAAGGAACCAATGA	50717
rs547535219	snp	A/C	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160230615	CTATTTCTGAATTGA[A/C]AACCAGTATTTAAAA	50717
rs547712029	in-del	-/G	0.0019996	0.0315563	intron-variant, nc-transcript-variant	DCAF8	GRCh38.p7	1:160262240	CCGGCTGGGAAGCGA[-/G]GGGGGGCGCAGGCCG	50717
rs547745591	snp	C/G	0.00199481	0.0315187	intron-variant	DCAF8	GRCh38.p7	1:160245505	CTTCATTAAAAGTAT[C/G]CTCTGTCAAAAGACA	50717
rs547847599	snp	A/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160220545	TGTCTGAATGCCAGG[A/T]CTTATCCTGTCAATA	50717
rs547915187	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160254531	AGGTACCATGGCTCA[C/T]GCCTGTAATCCCCAC	50717
rs547952028	snp	C/T	0.00398564	0.0444627	intron-variant	DCAF8	GRCh38.p7	1:160221254	TGTCAAGAAAAAATT[C/T]ACTGGCCCCTTCTGA	50717
rs547956686	snp	G/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160224030	TACTACCACCATTCC[G/T]CCTCTTCTGCCTCAT	50717
rs547981048	snp	A/C	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160260441	CAGTCATCAGATGGA[A/C]TAAAACTCACCAGTG	50717
rs548012627	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160253613	AGATCGCACCATTGC[A/G]CTCCAGCCTGTGCGA	50717
rs548043335	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160237665	CCAAGTAGCTGGGAC[C/T]AGAGGCACAAGGCAC	50717
rs548047915	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160221891	GCTCTTCATTCCCTA[A/G]CTCGATTCTCACTCT	50717
rs548103899	snp	C/G	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160244860	GTGATCCGCCCGCCT[C/G]GGCCTCCCAAAGTGC	50717
rs548144955	snp	G/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160252626	AAAGATAATAAGATG[G/T]ACTGAAATGAAGGAA	50717
rs548151914	snp	C/T			utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	DCAF8	GRCh38.p7	1:160262515	GCGCTGCCACGCTTT[C/T]CGGCCCCGTTTGCGA	50717
rs548196683	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160230464	TGTCTGTTTTCCTTA[A/G]GTCATGTCTCAAGAG	50717
rs548308581	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160224615	GACCAGGAGGTGGGG[A/G]TTGGGGTGGGGCTTC	50717
rs548360161	snp	C/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160253003	AATTATCTGTACAGA[C/G]AAACTTCAAAATCAA	50717
rs548390704	snp	A/C	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160226103	ATTTTAAGTGGCAAT[A/C]CTCAATTCTGTCAGT	50717
rs548451805	snp	C/G	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160226858	TAATTATATCCATTT[C/G]TTAAGTAGGTGTAAG	50717
rs548506775	snp	G/T	0.00119737	0.0244387	intron-variant	DCAF8	GRCh38.p7	1:160244837	CCAGGATGGTCTCGA[G/T]CTCCCGAGTGATCCG	50717
rs548571241	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160251851	ACTCATTATATAAAG[C/T]ATGTTTATGGTAGGT	50717
rs548579569	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160217888	CAACTATTCAACTCA[C/T]TGTAGCGTGAAGGCC	50717
rs548631663	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160250323	ACAAAAATATTAGCC[A/G]GGCGTGGTAGTGCAT	50717
rs548651037	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160235082	TATGTCCTATGTAAA[C/T]CATTGCCATCCCTTA	50717
rs548787899	snp	A/C/G			intron-variant	DCAF8	GRCh38.p7	1:160233277	CAGAGGACCAGGTGT[A/C/G]GTGGCTCATGCCTAT	50717
rs548904057	snp	A/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160218694	GCCCCCTGGAGCAGG[A/T]CTATTCCTACAGAGG	50717
rs548941602	snp	C/T			utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160216255	CATGAAGTTGGATGG[C/T]TTAATGATCAAGCAG	50717
rs549043635	snp	A/G	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160247824	AAAGAACCTCAATCC[A/G]TACATTGTACAATAT	50717
rs549051740	snp	A/C	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160222284	ACTTAGTTTAGTTTA[A/C]AGGGAAGAGACATGG	50717
rs549101448	in-del	-/TG	0.0023933	0.0345097	intron-variant	DCAF8	GRCh38.p7	1:160251669	TGGTGGTGGGGAACA[-/TG]TTGCCCAGGCTGGTC	50717
rs549168325	snp	C/T	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160241709	GCTATAAATTTTATC[C/T]GCCAGAAGTAAAAGC	50717
rs549229449	snp	A/C	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160248356	ACTGTTACAACAATG[A/C]AAAGACAAGCTACAG	50717
rs549241509	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160221506	AAGAAAATTTGAAAT[A/G]CCCTTTCACCAGGGC	50717
rs549336018	snp	A/G	0.00159617	0.0282053	intron-variant	DCAF8	GRCh38.p7	1:160255820	ACACAGGGTTTTGCT[A/G]TGTTGGCTAGGCTGG	50717
rs549502921	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160217102	GGTTGCTGGGGGTGG[A/G]GGGGGAGCCAACTGT	50717
rs549590669	snp	C/G/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160249145	CAAGTGAGCTGAGAT[C/G/T]GCACCACTGCACTCC	50717
rs549680656	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160232169	GAGCAGAGATCATGC[C/T]ACGGTACTCCAGCCT	50717
rs549743365	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160231508	CTAATAAGAAACCAA[A/G]GAGATTCTCATTTGG	50717
rs549766015	snp	G/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160234200	CTCTGACAAGATCAT[G/T]CCACTGTACTCCAGC	50717
rs549857312	snp	A/G	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160236075	AAAAAATGGTGGGGC[A/G]GGGGTGACTGAGGGA	50717
rs550015534	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160255014	GTAGCCATTTATATT[A/G]TTTTTCTAGTTTCCC	50717
rs550180095	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PEA15, DCAF8	GRCh38.p7	1:160215220	TTTCAGCAGAGTCTA[A/G]TAGTTTCTCTGTAAG	50717
rs550294464	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160219562	AACCTTGCACATCCC[A/G]GGGGGAACATCCTAC	50717
rs550302469	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160232059	AGCCAGGCGTGGTGG[C/T]GCATGCCTATCATCC	50717
rs550449296	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160223006	TTAGCAGCAGCCTTA[A/G]TCTCTCAAGTTTATA	50717
rs550461810	snp	C/T	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160244269	CAAGTGCCATCTCTT[C/T]ACTTCACTCACTGAG	50717
rs550535691	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160238364	GATCTCCAAACCAAC[C/T]AGGGCTTAGCTTAGG	50717
rs550548445	snp	C/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160258159	TGAAACCAGCCTGGG[C/G]AATATGGTGAAACCT	50717
rs550755465	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160255871	GTGATCCGCCCGTCT[C/T]AGCCTCCCAAAATGC	50717
rs550761860	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160223985	TGGGAACCACAGACA[C/T]GGAACAAAACAGGCC	50717
rs550769994	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160227768	TGTGTTCCAATAAAA[C/T]TTTATTTATAAAAAC	50717
rs550822860	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	DCAF8	GRCh38.p7	1:160263389	AGCACTTTGGGAGGC[A/G]GATGTGGGCGGATCA	50717
rs550830765	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160238358	CTCAAAGATCTCCAA[A/C]CCAACTAGGGCTTAG	50717
rs550874178	snp	C/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160235831	GCAACCTCCACCTCC[C/G]AGGTTCAAGCGATTC	50717
rs550891442	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160256069	TTGCTATGTTGCCAG[C/T]CTGAAACTCCTGGGC	50717
rs550935596	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160243177	AGAGCTGGTTAAATA[A/G]CCCAGGTGGTAGTTA	50717
rs550937474	snp	C/T	0.0103295	0.0711199	intron-variant	DCAF8	GRCh38.p7	1:160235226	GCAACCTCCACCTCC[C/T]GGGCTCAAGCGATTC	50717
rs550975367	snp	A/G	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160225273	TGATGAAACATGACC[A/G]CCTCAGGGGGTAGCA	50717
rs550999032	snp	C/T	0.00199481	0.0315187	intron-variant	DCAF8	GRCh38.p7	1:160242481	GTAGAAAAGAAAAAA[C/T]AAAACACCAAAACAT	50717
rs551024198	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160248962	TTTGGGAGGCTGAGG[C/T]GGGCAGATCACCTGA	50717
rs551213115	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160219795	GACTTGGAAACATGA[A/G]CTTCCCTAAGGGAAG	50717
rs551239134	snp	A/G	0.0146672	0.084371	intron-variant	DCAF8	GRCh38.p7	1:160235792	CACTCAGGATGGAGT[A/G]CAGTGGCATGATCTC	50717
rs551380867	in-del	-/T	0.00119737	0.0244387	intron-variant	DCAF8	GRCh38.p7	1:160245225	TATAAAACATTCATA[-/T]TTTTTTTCAGAGCCT	50717
rs551427112	snp	A/T	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160241738	GCTGTCAGGAAAGGC[A/T]GACCATCCAGTATGA	50717
rs551556776	snp	C/G	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160252319	TGTTGTGGTTGAACA[C/G]AGGAAAAGATTATAT	50717
rs551567981	snp	G/T			intron-variant	DCAF8	GRCh38.p7	1:160234772	TGTAGTTCAAAAGAT[G/T]AAATGATTTCCTCAA	50717
rs551676466	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	DCAF8	GRCh38.p7	1:160262579	CGCGCGAGCTCACGG[C/T]TCGCAACCCTCCTCG	50717
rs551739080	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160248835	GGAGTTCAAGGCTGC[A/G]GTGAGCTATGATCCT	50717
rs551810211	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160221394	AGGGAAGAGTGAGAC[A/G]CACCTTGAACTTCTA	50717
rs551953515	snp	C/T			utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160217245	CCACCCCTCCCCCAG[C/T]CCAAGAAACAAGGGA	50717
rs551955432	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160259256	AAAGAACTCTTTGGC[C/T]GGGCATGGTGGTTCA	50717
rs552013634	snp	A/G	0.00914312	0.0669923	intron-variant	DCAF8	GRCh38.p7	1:160259530	GAGCAAGACTCGTCA[A/G]AAAACAAACAAACAA	50717
rs552018756	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160255220	CATGTTCTACGAACT[A/G]CAGTAAGACAATCTA	50717
rs552100795	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160232853	ACCCAGCTTAAAATA[C/T]GCACACTGAAAACTG	50717
rs552207592	snp	C/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160245824	TATCTTCTCCATCTA[C/G]AGTTTAAAATTATAT	50717
rs552240633	snp	A/C	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160229766	GTGGCTCATGCCTGC[A/C]ATCCCAGCACTTTGG	50717
rs552278852	snp	C/G	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160225895	GTCACCCAGGCTGTA[C/G]TGCAGTGGCATGACC	50717
rs552292141	snp	A/G	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160244317	TCAGATGCGAAAGTG[A/G]GAACTAAAATAAAAC	50717
rs552338394	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160259161	TTGCCAAAAAGATAC[A/G]AAAGAAAAGCCAACA	50717
rs552339632	snp	C/T	4.97211e-05	0.00498579	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160217607	TCAAGATGGCATGCA[C/T]TGCACCCGGTCAGGG	50717
rs552353545	snp	A/C	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160250804	ATTTAAGTAGCTCAA[A/C]GTTGTTCTTGTGGTT	50717
rs552421201	snp	A/G	0.00279162	0.0372561	intron-variant	DCAF8	GRCh38.p7	1:160250127	CTCAAAAAAGGATAA[A/G]TTTTACTGTATATAA	50717
rs552427413	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160219496	GCTGAGAAGAGGAGG[C/T]TGAGTTGCAGGGAGT	50717
rs552555727	snp	A/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160228988	GGCTACCTGCTTGTG[A/T]AGGATCAGCGTGCCT	50717
rs552563992	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160258084	GGGTGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC	50717
rs552607434	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160246304	AAAGCAGCTGCAGAG[A/C]ACCTCTCTCAAAACC	50717
rs552638727	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160220888	GTAACCCCCACTGCT[A/G]GAAAATTAGGACCAA	50717
rs552696420	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160244520	GTCAGATTCTGAGTA[C/T]CATTTTACACACAAA	50717
rs552730610	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160259288	ACCTGTAATCCTAGC[A/C]CTTTGGGAGGCTGAG	50717
rs552859554	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160257502	CTATTACTCCCCTGA[C/T]AGAATACAAGACTTA	50717
rs552934736	snp	A/G	0.046775	0.145601	intron-variant	DCAF8	GRCh38.p7	1:160236286	CACACATACATACAC[A/G]TACGTATATATATAC	50717
rs552997971	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160243700	TTCTGCCCATCCTTA[C/T]AGCTTTATAGAACTC	50717
rs553029526	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160244648	TTTGAGACAGAGTCT[C/T]ATTCTGTCGCCCAGG	50717
rs553069096	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160251032	TCATGGTTTATATAA[C/T]CCCAGCATTCTCTCA	50717
rs553195780	snp	A/G	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160257627	TGTTTTAAACTGGCA[A/G]CAAAGAGGCTGCTTT	50717
rs553209786	in-del	-/CC	0.00478085	0.0486577	intron-variant	DCAF8	GRCh38.p7	1:160228909	ATTCAGTTGGCTGCA[-/CC]CAGGAGAGGTGCCAG	50717
rs553416781	snp	C/T	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160248143	AAACCCCCGTCTCTA[C/T]TAAAAATACAAAAAT	50717
rs553542532	snp	A/G	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160234792	GATTTCCTCAAAGTC[A/G]GATAACTACAAAGCT	50717
rs553627512	snp	A/G	1.64928e-05	0.00287161	intron-variant	DCAF8	GRCh38.p7	1:160222790	CCTTTTACTGAAATG[A/G]TAAATGAGGGAAGAA	50717
rs553677421	snp	C/T	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160253112	AATCTTGAGGAATAC[C/T]TACCCTTAGAGAAGA	50717
rs553689013	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160223293	AAGAAGCCAAGAGTT[C/T]CAATGACTATGGTCA	50717
rs553738942	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160252390	GCTTTTAAGATGGGC[C/T]TTAAAAGACAGGCAG	50717
rs553746603	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160245965	GCAACATGGAGAAAC[C/T]CTGTCTCTACTAAAA	50717
rs553804996	snp	C/T	3.30147e-05	0.00406279	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160217701	CCAACCCCAGGTTCT[C/T]GCCAGCGCTGTGGAT	50717
rs553806208	snp	C/T	0.00119737	0.0244387	intron-variant	DCAF8	GRCh38.p7	1:160259289	CCTGTAATCCTAGCA[C/T]TTTGGGAGGCTGAGG	50717
rs553870277	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239440	TGTGCTTATACTACA[C/T]TGCCTCCTACCAGCA	50717
rs553944216	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160257071	AATGATGTTTCTTGG[C/T]TACATTTGTAAAAAT	50717
rs553948350	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160231034	GTCGAGATTACAGGT[A/G]TGAGCCACTACACCT	50717
rs553957641	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160229955	TTGAACCCGGGAAGC[A/G]GAGGTTGCAGTGAGC	50717
rs553965250	in-del	-/ATAATT	0.00199481	0.0315187	intron-variant	DCAF8	GRCh38.p7	1:160236188	AAAAAAGAAACTAAA[-/ATAATT]ATAATTATAAGCTAA	50717
rs554067156	in-del	-/AA	0.0437281	0.141251	intron-variant	DCAF8	GRCh38.p7	1:160256902	TACAGAGGTAGAGAT[-/AA]AAAAAAAAACTGCTG	50717
rs554086447	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160219073	TTGATCAGGGCTGAG[A/G]CAGCTGCTGGGGAAG	50717
rs554220573	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160222508	AAAACTCAGCACCTC[C/T]AGGCTAACTAGTCTT	50717
rs554277313	snp	A/T			intron-variant	DCAF8	GRCh38.p7	1:160256674	GGATAAACAGCAAAT[A/T]TCTAATCTAAAATGT	50717
rs554402018	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160248745	ACTAAATAATTATCG[C/T]GAGCTGGATATGGTG	50717
rs554405605	in-del	-/G			intron-variant	DCAF8	GRCh38.p7	1:160252572	AAAAGCTTTGTTGTT[-/G]GGGGGCAGGCAGTCA	50717
rs554488481	snp	A/G			utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160217444	TGGTTCACTCCTCTG[A/G]TTTGTCCTTCTCCTG	50717
rs554525404	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160258575	GAGCATCACTTGAGC[C/T]GGGCAAGTAAGACCT	50717
rs554614227	snp	C/G	0.00597247	0.0543191	intron-variant	DCAF8	GRCh38.p7	1:160230838	CTCATTGCAACCTCT[C/G]ACTCCTGAGCTCAAG	50717
rs554676211	snp	C/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160238460	TGGCTGCTTTTGCTC[C/G]TTTCTTAACCACAAA	50717
rs554678011	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160230094	ATTTTGAAGGCATGG[A/G]AATAGGGGAAGAAGA	50717
rs554739749	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160237806	CAGCCTCCCAAAGTA[C/T]TGGGATTACAGGCAT	50717
rs554755378	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160224262	GCAAGAGATGCTCTT[A/G]AGCGCTTTCTCCTCT	50717
rs554810425	snp	C/T	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160229047	GCTCACGACTGTAAT[C/T]CCAGCACTTTGAGAG	50717
rs554873153	snp	G/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160251286	TCCAAAGTACAAATT[G/T]GCTTTTCTAGGTCCC	50717
rs555154194	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160228305	TGCCTTCAGGCACCC[A/G]CTAACTTGTTACCCT	50717
rs555216548	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160232409	GCACTTTGGGAAGCC[A/G]AGGTGGGTGGATCAT	50717
rs555290298	snp	A/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160220816	TACATTCTACTCTAC[A/T]TTTACAATTTGCATG	50717
rs555341784	snp	C/G	1.98328e-05	0.00314897	intron-variant, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239574	AGGGGAGCCAAAGTA[C/G]GGCCATGTCCCGATA	50717
rs555539486	snp	C/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160246641	CTATAAATCAGTCAA[C/G]GAGGCAGAGATGCTG	50717
rs555603199	snp	A/G	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160254044	AAAATTATTTCCTGG[A/G]ATGGGTGCGTGGCTC	50717
rs555605836	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160254546	CGCCTGTAATCCCCA[C/T]ACTTTAGGAGGCCGG	50717
rs555732768	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160247246	TAAAAATAACCATAA[C/T]TCCTGCCAAACTGAA	50717
rs555859053	snp	A/G	0.00159617	0.0282053	intron-variant	DCAF8	GRCh38.p7	1:160254490	TCATCTCTTGGCTTT[A/G]AAAAGCCCTGGTTTT	50717
rs555946382	snp	C/T	1.66957e-05	0.00288922	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240177	ATGACCAGTGTCCTC[C/T]ATGCTGTCAGAGTCC	50717
rs555995113	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160224600	GCTGAAAAAAGCAGG[C/G]ACCAGGAGGTGGGGG	50717
rs556134067	snp	C/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160246020	GCACATGCCTGTAAT[C/G]CCAGCTACTAGGGAG	50717
rs556205762	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160237044	ACAAAGGTACTATTC[A/G]GATGAACCAGAGTTA	50717
rs556268467	in-del	-/T			intron-variant	DCAF8	GRCh38.p7	1:160235741	AATTACTTACAATGA[-/T]TTTTTTTTTTTTTCT	50717
rs556324476	snp	G/T			intron-variant	DCAF8	GRCh38.p7	1:160223758	CAAAAATTAGCCAGG[G/T]GTAGAGGCATGCACC	50717
rs556341853	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160253227	GAGGATAGGCTGGGC[A/G]CAGTGACTCATGCCT	50717
rs556364581	snp	A/G	1.64743e-05	0.00287	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160218924	ATGGTCTAGGCCACT[A/G]GTTGCCAGCACAGGC	50717
rs556403576	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160259884	CACCAATATCTAATA[C/T]TCTCTGTCCTCTGGT	50717
rs556476592	snp	A/C	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160226248	ACTCACGGGCAGAAA[A/C]CATGCTTAATGTAAG	50717
rs556513023	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160253966	GAGATTGAATGGAAT[A/G]CTGATTTTCTCTCCA	50717
rs556534073	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160242762	AGACACTACATAAAC[A/G]AACAGGCATGACTGT	50717
rs556622858	snp	C/T	0.00119737	0.0244387	intron-variant	DCAF8	GRCh38.p7	1:160222425	TCTTCCCTAAGATCC[C/T]TTTCTTGTCTCAATA	50717
rs556677811	snp	G/T	0.00199481	0.0315187	intron-variant	DCAF8	GRCh38.p7	1:160250240	AGGCCAAGGCGGGCA[G/T]ATCACCTGAGGTCAG	50717
rs556837719	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160258420	TCTTAGCCTCCCACT[C/G]TAATCATCCTAGGAA	50717
rs556852795	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160257473	TTTAATAGTCACTTT[A/G]TGATTTTAAAAGCCT	50717
rs556927630	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160230784	TGAGACAGAGTCTCG[C/T]TCTGTCATTCAGGCT	50717
rs556941266	snp	A/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160230388	CTGGATAGGGATGGA[A/T]ACAGCTTATTACTAA	50717
rs556975421	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160249364	AAGTACTAACAAGAA[A/G]TAGAGCAACTACAAC	50717
rs557044904	snp	A/G	0.00159617	0.0282053	intron-variant	DCAF8	GRCh38.p7	1:160257075	ATGTTTCTTGGCTAC[A/G]TTTGTAAAAATAAAA	50717
rs557179532	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	DCAF8	GRCh38.p7	1:160264385	GGGAGAGACACACAG[A/G]TAATAAAGTTATAAA	50717
rs557206711	snp	A/G/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160248482	GGCTCACGCCTGTAA[A/G/T]CCCATCACTTTGGGA	50717
rs557237024	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	DCAF8	GRCh38.p7	1:160263642	GACTCCGTCTCAAAA[A/T]AAAAGTAATGTCGTA	50717
rs557267962	snp	A/G			utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160216116	AGTGCCCAAGCTCCA[A/G]CCACTGTAATCAGTC	50717
rs557324154	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160248654	GTTGCAGTGAGCTGC[A/G]ATCGCGCCACTGCAC	50717
rs557390334	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160254670	GGTGGCATGCGCCTG[C/T]AGTCTTAGCTACTCG	50717
rs557457817	snp	C/T	0.00159617	0.0282053	intron-variant	DCAF8	GRCh38.p7	1:160257063	TTAACAGCAATGATG[C/T]TTCTTGGCTACATTT	50717
rs557461094	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160233862	GGGGCATGCAGAGGT[A/G]CTATAAAAATGATTA	50717
rs557527919	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160248110	CAGGAGTTCGAGATC[A/G]GCCTGGCCAACATGG	50717
rs557590881	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160255309	TAGATTTTTTTACTA[C/T]TATTATCGTAGAGAC	50717
rs557788731	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160256354	GATGCTCCCAAGGTA[C/T]AACTTACAATAAAAC	50717
rs557935401	snp	A/T	8.81158e-05	0.00663703	intron-variant	DCAF8	GRCh38.p7	1:160240405	GAGTAGAGGAGAGGG[A/T]AAAATAAGAAAACAG	50717
rs557971666	in-del	-/TG			intron-variant	DCAF8	GRCh38.p7	1:160236357	ATATGTGTGTACATA[-/TG]TGTGTATATAAACAT	50717
rs558006971	snp	A/G			upstream-variant-2KB	DCAF8	GRCh38.p7	1:160263512	GGCATGGTGGAGCGC[A/G]CCTGCAATCCCAGCT	50717
rs558068409	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160219801	GAAACATGAGCTTCC[C/T]TAAGGGAAGGGCAGG	50717
rs558116672	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160219551	CTGCTTGAGAGAACC[C/T]TGCACATCCCAGGGG	50717
rs558135123	snp	C/G	0.00199481	0.0315187	intron-variant	DCAF8	GRCh38.p7	1:160240972	GATCGAGACCATCCT[C/G]GCTAACATGGTGAAA	50717
rs558140812	in-del	-/A	0.00119737	0.0244387	intron-variant	DCAF8	GRCh38.p7	1:160230447	GGAGACTGAATCCAC[-/A]GTGTCTGTTTTCCTT	50717
rs558147401	in-del	-/A	0.00119737	0.0244387	intron-variant	DCAF8	GRCh38.p7	1:160253876	ATAGTCCATGCTTCC[-/A]AAAAAAATACAGAGA	50717
rs558179781	snp	C/G	0.00119737	0.0244387	intron-variant	DCAF8	GRCh38.p7	1:160260980	AAAAAATATGATCGA[C/G]ACAAAGACAAAATAC	50717
rs558247887	snp	A/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160248007	AGTTGGATTTATCAA[A/T]ATTAATAAATTCTGA	50717
rs558448469	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160254092	ACTTTGGGAGGCCGA[A/G]GCAGGCGGATCATGA	50717
rs558468522	in-del	-/AAG			intron-variant	DCAF8	GRCh38.p7	1:160249359	TTATTAAGTACTAAC[-/AAG]AAGTAGAGCAACTAC	50717
rs558524748	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160258377	CACTTTAAGAGGTTG[A/G]TGGTGGGAACTAAAA	50717
rs558590722	snp	C/T	0.00199481	0.0315187	intron-variant	DCAF8	GRCh38.p7	1:160236628	AAGATGTTGTGTTTT[C/T]TCTATGATACCACAC	50717
rs558610537	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160217362	GAGGCCATTTCTGCC[A/G]AGTCCTATGCACCTC	50717
rs558612438	snp	A/G	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160226213	GCTTTTTACATGTAC[A/G]TTACCTACCGAAAAA	50717
rs558654646	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160244923	CCAACTAACTTCAAA[C/T]TTATTAAAGGCACAG	50717
rs558675701	snp	A/C	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160217946	GGCTGCAAGCCAATG[A/C]AACTTTATTTACAAA	50717
rs558731786	snp	A/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160243415	AATCACCTTTTTTTT[A/T]TTTTTTTTTAAAAAG	50717
rs558760222	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160228177	AGCTATCCTCCAGCT[C/T]TGGCCTTCCAAAGTG	50717
rs558850236	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160242102	TACAAAAAATTAGCC[A/G]GGCGTGGTGGCATGT	50717
rs559050058	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160235101	TGCCATCCCTTACTC[A/G]ATACTGGTACTGACC	50717
rs559066163	snp	G/T	0.00398564	0.0444627	intron-variant	DCAF8	GRCh38.p7	1:160235106	TCCCTTACTCAATAC[G/T]GGTACTGACCTATAA	50717
rs559110262	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160235394	AAAGTGCTGGGGTTA[C/T]AGGCATGAGCCACTG	50717
rs559147345	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160235567	TTTTATGGTCCAACA[C/T]AGAAAAATCTCCCAC	50717
rs559198471	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160243254	CCAGTGATTTGACAC[C/T]TGGCAGCACTGGTCC	50717
rs559299070	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160242052	GTTCAAGACCAGCCC[A/G]GCTAACATGGTGAAA	50717
rs559468549	snp	G/T	0.00119737	0.0244387	upstream-variant-2KB	DCAF8	GRCh38.p7	1:160263891	CATGTCCCAGCCCTA[G/T]GGTTTTTTTCCTTTT	50717
rs559655327	in-del	-/CTGCTATCTCCAAGACAAAAT	0.0023933	0.0345097	intron-variant	DCAF8	GRCh38.p7	1:160223428	AAAACTAACCTCTAA[-/CTGCTATCTCCAAGACAAAAT]CATGACAGGTATCTG	50717
rs559757416	snp	C/T	0.00159617	0.0282053	intron-variant	DCAF8	GRCh38.p7	1:160241402	TTATTAGGAAGCATA[C/T]ATAAAATTGATAAAA	50717
rs559758177	snp	A/G	0.00199481	0.0315187	intron-variant	DCAF8	GRCh38.p7	1:160255867	TCAGGTGATCCGCCC[A/G]TCTCAGCCTCCCAAA	50717
rs559829400	snp	G/T	0.00199481	0.0315187	upstream-variant-2KB	DCAF8	GRCh38.p7	1:160263032	GGTGGTGTGGGTAAA[G/T]GTTCCCAAGAGTGGG	50717
rs559883261	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160221312	AATTCCCATTAAGAC[C/T]CAAGTGTTTTGGGTT	50717
rs559946850	snp	A/C	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160222085	TTGAATGTACGCATG[A/C]CATTTCACCCCTAAA	50717
rs559987557	snp	C/T	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160234002	TAATTACAGATGAGA[C/T]CAAAGGATTTCTTTG	50717
rs560026743	in-del	-/AGA			downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	PEA15, DCAF8	GRCh38.p7	1:160215725	AGAGCAGCAGTCGGG[-/AGA]AGAAAAGCTTTACTG	50717
rs560069833	snp	A/C	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160260226	CTTTTAGAGTTGTGG[A/C]AATTAAGAGTCAGAG	50717
rs560164354	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160251459	CTTCCACACTCTAAT[A/G]GCATAGTGGTTTTGC	50717
rs560170714	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160252684	ATTATAGTTGCCAAG[A/G]TAAGAAGTAATGAGG	50717
rs560215418	snp	C/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160237099	TGTTCAAGGCTAAGA[C/G]ATACAGTTCTGTAAT	50717
rs560289430	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160257948	TGCCTAGGCTGGACT[C/T]GAACAACTAGGATCA	50717
rs560351881	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160225733	AGCTGCAATTTGATG[C/T]AGTGGCAGGAAACTG	50717
rs560390878	snp	A/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160230378	AATAGGCCAACTGGA[A/T]AGGGATGGATACAGC	50717
rs560734600	in-del	-/G	0.00478562	0.0486817	intron-variant, nc-transcript-variant	DCAF8	GRCh38.p7	1:160262240	CGGCTGGGAAGCGAG[-/G]GGGGGGCGCAGGCCG	50717
rs560745427	in-del	-/GTGGGCTTAA	0.00199481	0.0315187	intron-variant	DCAF8	GRCh38.p7	1:160237618	TAAAGCCTCAACCTT[-/GTGGGCTTAA]GTGATCCTCCCACCT	50717
rs560789887	snp	A/G	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160248963	TTGGGAGGCTGAGGC[A/G]GGCAGATCACCTGAG	50717
rs560846481	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160258962	AGAGTTCATAAAAAC[A/G]CAAATGATACAAATG	50717
rs560862389	snp	A/T	0.00159617	0.0282053	intron-variant	DCAF8	GRCh38.p7	1:160235400	CTGGGGTTACAGGCA[A/T]GAGCCACTGCACCTG	50717
rs560992998	snp	A/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160257902	GCTTGGCTTTTTTTT[A/T]AAACTTTTTGTAGAG	50717
rs561056286	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160257388	TAATCTGGATATTTC[C/T]TAGACATGTTTAGAA	50717
rs561060919	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160236756	CAAATTTTATGTTTG[C/T]ATGTTTCTATAAATA	50717
rs561089846	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160222937	CCAGTCCCAAGAGAT[A/G]ATTTATATTCTCCCA	50717
rs561198945	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160244712	AAGCTCTGCCTCCCG[A/G]GTTCACACCATTCTC	50717
rs561278904	snp	G/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160235414	ATGAGCCACTGCACC[G/T]GACCAAGATTTGTTA	50717
rs561361092	snp	C/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160223677	TCGAGGCAGGCGGAT[C/G]ACTTGAGCCCAGGAG	50717
rs561398479	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160254799	ATCTAAAAAAAAAAG[A/G]AAAAAGAAAAGTCCT	50717
rs561424324	snp	A/G	0.00159617	0.0282053	downstream-variant-500B	PEA15, DCAF8	GRCh38.p7	1:160215589	AAGCACTGGAAATAC[A/G]GGTCTCCCAAAATGG	50717
rs561461859	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DCAF8	GRCh38.p7	1:160262171	GGTCGGCGGAAGGAA[A/G]AGACCTGAGCGCTAA	50717
rs561580513	snp	G/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160246921	CTGTGATTATACCAC[G/T]TCTCTCCAGGCAGGA	50717
rs561618729	snp	C/T	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160219231	ATATGGCCCTAGGGG[C/T]GGGTGAGTGGACTGC	50717
rs561683967	snp	G/T	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160231932	ATGGTGGCTCATGCC[G/T]GTAATCCCTACACTT	50717
rs561691553	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160226778	CCTATTCACTTCTCA[A/G]TCCATCCTAATCTGG	50717
rs561714006	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160247549	AGAGACTACGTATCC[C/T]TTGTCCGGTGTATCC	50717
rs561732229	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160229170	GCAAAGTGGCACATG[C/T]CTGTAATCCCAGCTA	50717
rs561752928	snp	C/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160218503	CCGGGACCTGATCAA[C/G]AAGGCTGATCTCCTA	50717
rs562038162	snp	A/G			utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	DCAF8	GRCh38.p7	1:160262518	CTGCCACGCTTTCCG[A/G]CCCCGTTTGCGACGA	50717
rs562128492	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160245475	CTCCGCTACCCTCTA[C/T]AGAAATCTAAGCTGC	50717
rs562171637	snp	G/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160221099	CACCTGGGCAAATGG[G/T]TTAATCATCAAACCC	50717
rs562233349	snp	C/T	0.00159617	0.0282053	intron-variant	DCAF8	GRCh38.p7	1:160246069	CTTGAACCTGGGAGG[C/T]GGAGGTTGTGGTGAG	50717
rs562290313	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160258801	TTACAGTGTGGTCCA[C/T]AGACTAGAAATACTG	50717
rs562293125	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160253386	TGACGTCTAAGTGAC[A/G]CTGGTAATCCCAGCA	50717
rs562320770	in-del	-/G			intron-variant	DCAF8	GRCh38.p7	1:160256557	AGTAGCTTTCCAGAT[-/G]GCTAAGAAAAAGCCA	50717
rs562377772	snp	C/T	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160259401	AGCTGGGCATGGTGG[C/T]GCATGCCTGTAATCC	50717
rs562388250	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160253509	AAAAATTAGCCACAC[A/G]CGGTGGCATACGCCT	50717
rs562395510	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160221895	TTCATTCCCTAACTC[A/G]ATTCTCACTCTTCCT	50717
rs562450770	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160260357	TACTTTTCTCTTTAT[A/G]TCTTACTGATACACA	50717
rs562455788	in-del	-/T	0.464309	0.12873	intron-variant	DCAF8	GRCh38.p7	1:160243406	CCTTATGTAATCACC[-/T]TTTTTTTTTTTTTTT	50717
rs562487073	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160254151	ACATGGTGAAGCTCC[A/G]TCTCTACTAAAAATA	50717
rs562499051	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160217513	GCGTTTCTGCTGAAT[A/G]TAGGGCCTGGGACAG	50717
rs562522505	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160262069	CAACGAAGCAAGGCG[C/T]CCCTGTGAACTGTGC	50717
rs562538140	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160238043	ACTCCAGGTCCACCT[A/G]TATTTTTGCTTAGGG	50717
rs562553742	snp	A/C	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160261190	AAGCTCTTTGGGAAA[A/C]TGGTAGGAATTTTAT	50717
rs562601443	snp	A/G	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160245422	CCCTTTCATTCCCAT[A/G]ACAATTATTCCAGAA	50717
rs562633782	snp	C/T	1.70067e-05	0.002916	intron-variant	DCAF8	GRCh38.p7	1:160225682	CAGTTGGAAAAGCAA[C/T]GAAAATGTAAAAATG	50717
rs562770926	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160231162	CGTGTAAGATTTTTG[A/G]AAAACGGTAAAAAAT	50717
rs562849380	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160249236	TAATCCCTTGAAAAG[A/G]TCCTCAACATTATTA	50717
rs562902501	snp	C/T	0.00119737	0.0244387	intron-variant	DCAF8	GRCh38.p7	1:160220940	AGTAAAAGACCACAT[C/T]GATCATTCAGCTTAC	50717
rs563005125	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160242178	TGAACCTGGGAGGTG[A/G]AGGCTGCAGTGAGCC	50717
rs563019275	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160252506	AAACATATATGGGTA[A/G]TCTACTTTGGCTAGA	50717
rs563067111	snp	G/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160241583	CAATGAGAACTTGAG[G/T]AATGTTCTAAAGCCA	50717
rs563128292	snp	A/C			utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160215901	GCTGGGAAAAGGGGC[A/C]GGAGGAAGAAGTATC	50717
rs563208372	snp	A/G	0.00119737	0.0244387	intron-variant	DCAF8	GRCh38.p7	1:160258085	GGTGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA	50717
rs563270515	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160232903	AATCCAGAATAATCT[C/G]TCTAAAACAGCCATA	50717
rs563320204	snp	A/G	0.00914312	0.0669923	intron-variant	DCAF8	GRCh38.p7	1:160256471	TAACAAAACATACCT[A/G]GTAATGTGGCAATCA	50717
rs563395830	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160229033	AGCCAGGCGCGGTGG[A/C]TCACGACTGTAATCC	50717
rs563484290	snp	A/G	0.0240643	0.107019	intron-variant	DCAF8	GRCh38.p7	1:160248308	AGAGACTCCATCTAG[A/G]AAAAAAAAAAAATTA	50717
rs563547323	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160255800	AATTTTTATATTTTT[A/G]GTAGACACAGGGTTT	50717
rs563562153	snp	C/T	0.00199481	0.0315187	intron-variant	DCAF8	GRCh38.p7	1:160222150	TCTAAGTAATCAAAT[C/T]AATTTAATATTGAAT	50717
rs563583231	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	DCAF8	GRCh38.p7	1:160262950	GAGAGTCCCCATTTA[C/T]GTATTTTTAAAGAAG	50717
rs563643576	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DCAF8	GRCh38.p7	1:160262439	ACCACCAACGCCGCC[A/G]CCATCTTACACTGGC	50717
rs563726852	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160232123	GCTGAGGGAAGAGAA[C/T]CACTTGAGCCTGGTA	50717
rs563792771	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160248167	CAAAAATTAGCCGGG[C/T]GTGGTGGCACATGCC	50717
rs563796179	snp	A/C	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160222847	ATATACATTCATCTC[A/C]AAGGGAATTTAGTTA	50717
rs563869884	snp	A/G	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160240598	AAATACTTCAACAAA[A/G]GCAAAGAATCTCAGG	50717
rs563925341	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160246200	AGACCAGTGTAACAT[A/G]AAGAACAGATCTGAT	50717
rs564192244	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160261034	AGAAGACATGGGGCA[A/G]GGGGCACACATTCAC	50717
rs564294790	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160219108	GCCCACCCATCCTGA[A/G]CCTAAGCCAAAGGGC	50717
rs564323518	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160232187	GGTACTCCAGCCTGC[A/G]CAACAGAGCAAGACT	50717
rs564346686	snp	A/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	DCAF8	GRCh38.p7	1:160262268	CCGAGCCGGAACGAG[A/T]CACAGACCGGGTAGG	50717
rs564386159	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160229892	GCCAGGCGTGGTGGC[A/G]TGCACCTGTAATCCC	50717
rs564433780	snp	A/C	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160220226	TCTTTTAGGCAGTGC[A/C]GTTAAAGTCCAATGC	50717
rs564513070	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	DCAF8	GRCh38.p7	1:160239125	ATAGGGGGAATGTCA[C/G]GGAAGAAAAGAGAAC	50717
rs564554393	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160220596	GCTCTGGCCTTAGAT[A/G]ACTGGGCTGGGGGAA	50717
rs564570659	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160232007	ACCAGCCTGGCCAAC[A/G]TGGCGAGACCCCATC	50717
rs564578625	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160258625	ACAAACAAAAAAAAA[A/C]CAACCAAAAATTAGC	50717
rs564593530	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160244940	TATTAAAGGCACAGA[C/T]ACTAAGGATTATAGA	50717
rs564633806	snp	G/T	1.66743e-05	0.00288736	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239747	CCAGTACTGGCTGCC[G/T]CCGTACCCAATCCCA	50717
rs564662519	snp	C/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160246721	GCACGGCAGCTCACG[C/G]CTATAATCCCAGCAC	50717
rs564797024	snp	A/C	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160228686	TTTTTAATAACCCTA[A/C]ACTAAAATTCAGTAT	50717
rs564894850	snp	A/C	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160224325	CAATTCAGGATAATC[A/C]CTCAGTGCCCATGGC	50717
rs564921035	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160240807	CTTCTTAGCGAAAGA[C/T]GGAAACCAGCTGATA	50717
rs564960698	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160216698	ATTCAGAGAATATAT[A/C]GGTATTTAAACTTTG	50717
rs565010727	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160241413	CATATATAAAATTGA[C/T]AAAAAGCTGGGCTAC	50717
rs565066088	snp	C/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160243838	GTAGTTTCCTAAACT[C/G]AGAACAACACAGGAA	50717
rs565130679	snp	C/T	0.00199481	0.0315187	intron-variant	DCAF8	GRCh38.p7	1:160250422	GGTGAGCCAAGATCG[C/T]ACCATTGCACTCCAG	50717
rs565199654	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160249792	TGGTAGGTCCACACA[A/G]TGGGATACTACTGAG	50717
rs565262494	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160248868	TACTCACTGCACTCC[A/G]GTCTACGCAACAGAG	50717
rs565505208	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	DCAF8	GRCh38.p7	1:160264234	CCTATTCATTCTTTC[A/T]TTCATTCAGTCAACA	50717
rs565529266	snp	A/C	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160234521	ATAATCTGCCAAAGT[A/C]ATTCGCTCTATTCAT	50717
rs565602296	snp	A/C	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160234162	AAGAAAATCCCCCTT[A/C]TGCCAACTTCACACA	50717
rs565787981	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160241711	TATAAATTTTATCCG[C/T]CAGAAGTAAAAGCTG	50717
rs565880585	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160238229	GTGAACTGAGAGTTT[C/G]AGCAGGTAAGCTGAA	50717
rs565982409	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160240907	CGGTGGCTCACGCCT[A/G]TAATCCCAGCACTTT	50717
rs566050647	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160219687	CTGGGTAAATTCACT[A/G]AACAAGGCAAAAGAA	50717
rs566113672	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160220614	TGGGCTGGGGGAATG[C/T]AGAGAATGGGATCAA	50717
rs566122198	snp	G/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160255204	TCTTCTTTCAAGTAT[G/T]CATGTTCTACGAACT	50717
rs566175266	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160217361	AGAGGCCATTTCTGC[C/T]GAGTCCTATGCACCT	50717
rs566179133	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	DCAF8	GRCh38.p7	1:160262570	AAGAGTGGTCGCGCG[A/G]GCTCACGGCTCGCAA	50717
rs566183411	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160254495	TCTTGGCTTTGAAAA[A/G]CCCTGGTTTTTTTTT	50717
rs566211869	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160251505	TTTAAGACAGGGTCT[C/T]GCTGTTGTCCAGGCT	50717
rs566214340	snp	A/T			intron-variant	DCAF8	GRCh38.p7	1:160221645	CACAGCTAAGAAGGA[A/T]TAAAAAGGAAGAGAG	50717
rs566322894	snp	C/G	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160244864	TCCGCCCGCCTCGGC[C/G]TCCCAAAGTGCTGGG	50717
rs566365227	snp	C/T			upstream-variant-2KB	DCAF8	GRCh38.p7	1:160264225	CCCCACCGTCCTATT[C/T]ATTCTTTCATTCATT	50717
rs566367934	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160250579	CAAGGCTGTGATTAA[C/T]AGAAGTTGACAAAAA	50717
rs566403365	snp	C/T	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160232186	CGGTACTCCAGCCTG[C/T]GCAACAGAGCAAGAC	50717
rs566510416	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160224078	TCCTCCTTCCTAGAG[A/G]TATAAGGTCACTCCC	50717
rs566514040	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160252128	TGGCACCACCCAGTG[A/G]CCTATGTGTAAGCAA	50717
rs566562449	snp	A/G	0.00159617	0.0282053	utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160216082	GGGACTTTCAGACTC[A/G]GTGACCAGTGATAAG	50717
rs566564185	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160259101	GGTCTGAATGACACA[A/G]CTGCTTTCATTGTGA	50717
rs566575019	snp	C/G	0.00119737	0.0244387	intron-variant	DCAF8	GRCh38.p7	1:160251088	CTCAAGTGCCCAACT[C/G]TCCTACATAAACACC	50717
rs566636786	snp	A/G	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160258280	TAAGCCCAAGAGGTC[A/G]AGGTTGCAGTGAGCC	50717
rs566766523	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160249149	TGAGCTGAGATCGCA[C/T]CACTGCACTCCAGCC	50717
rs566835125	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160243328	GGAAAGAAGGGAGGG[A/G]AAGTAAGGAAAGGAA	50717
rs566870631	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160243344	AAGTAAGGAAAGGAA[A/G]TAAGGAGGGGAAAGA	50717
rs567035758	snp	C/T	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160242676	AGATAGTAAAAACCT[C/T]AGGCTTTGCAGACCA	50717
rs567049153	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160218698	CCTGGAGCAGGACTA[C/T]TCCTACAGAGGAAAT	50717
rs567218263	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160258492	AAAACCCTGGAAATA[C/T]AAAAATATCTTCAAG	50717
rs567308128	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160235740	AAATTACTTACAATG[A/G]TTTTTTTTTTTTTTC	50717
rs567312501	snp	A/G	0.0023933	0.0345097	intron-variant	DCAF8	GRCh38.p7	1:160258210	AAATTAGCCAGGTAC[A/G]GTGGCGTGCACCTGT	50717
rs567373593	snp	C/T	0	0	intron-variant	DCAF8	GRCh38.p7	1:160257577	TCTATACAATGTCTC[C/T]TACTAGAATCTGTTT	50717
rs567409375	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160227882	TGATAGGCCCTTGAT[A/G]GTTTATATTTTACTT	50717
rs567552585	snp	C/G/T	0.00159617	0.0282053	intron-variant	DCAF8	GRCh38.p7	1:160222329	TTGTGTAGGAGGGTA[C/G/T]GCCCTGAACACTAAC	50717
rs567591421	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160235842	CTCCCAGGTTCAAGC[A/G]ATTCTCCTGCCTCAG	50717
rs567623300	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	DCAF8	GRCh38.p7	1:160263476	CTCTACGAAAAATAC[A/C]AAAAAAAAAAAAAAT	50717
rs567650177	snp	A/G	0.00993419	0.0697739	intron-variant	DCAF8	GRCh38.p7	1:160235227	CAACCTCCACCTCCT[A/G]GGCTCAAGCGATTCT	50717
rs567824401	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160248512	AGGCCGAGGTGGGCA[A/G]ATCACGAGGTCAGGA	50717
rs567889492	snp	C/G	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160256072	CTATGTTGCCAGCCT[C/G]AAACTCCTGGGCTCA	50717
rs568096298	snp	G/T			intron-variant	DCAF8	GRCh38.p7	1:160256682	AGCAAATATCTAATC[G/T]AAAATGTTTGCATTG	50717
rs568100648	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239355	CAAAGGTAAAATAAC[C/T]TGGCCAAGATCACTG	50717
rs568137923	snp	A/G	0.00119737	0.0244387	intron-variant	DCAF8	GRCh38.p7	1:160245940	GGTCAGGAGTTCGAG[A/G]CCAGCCTGAGCAACA	50717
rs568161320	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160246360	GACTGCCTGAACTTT[C/T]GACTCATAATTGCTC	50717
rs568200005	snp	A/C	0.0023933	0.0345097	intron-variant	DCAF8	GRCh38.p7	1:160253052	CTCACTAAAACAAAC[A/C]ATTAGTTACCTAAGA	50717
rs568239788	snp	A/G	0.00279162	0.0372561	intron-variant	DCAF8	GRCh38.p7	1:160229851	ACACGGTGAGACCTC[A/G]GTTCTACTGAAAATA	50717
rs568287413	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160222339	GGGTACGCCCTGAAC[A/G]CTAACGCTTTTTCAT	50717
rs568303564	snp	G/T	0.0023933	0.0345097	intron-variant	DCAF8	GRCh38.p7	1:160237635	GGGCTTAAGTGATCC[G/T]CCCACCTCAGCTGCC	50717
rs568463362	snp	A/G	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160219569	CACATCCCAGGGGGA[A/G]CATCCTACTACTTGC	50717
rs568569993	in-del	-/CACA/CACACA			intron-variant	DCAF8	GRCh38.p7	1:160236254	ATTATGCTGAGGCAT[-/CACA/CACACA]CACACACAAACACAC	50717
rs568706782	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160221159	CCTGCAGAATGCTTT[C/T]GGAGAATGGACAAAT	50717
rs568739519	snp	C/T	0.000798403	0.0199641	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	PEA15, DCAF8	GRCh38.p7	1:160215806	TCACCCCACCAGCAA[C/T]AGGAACACAGACCAC	50717
rs568768130	snp	A/T			utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160217290	AAACCCCATTCCCTA[A/T]CCCAAACCAGTTAAC	50717
rs568921894	snp	A/C	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160245846	AAATTATATTAATTC[A/C]TATCAAGTGGGGAAA	50717
rs568926193	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160224012	GGCCAATCTTGGGCT[A/G]GTTACTACCACCATT	50717
rs568945850	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160252777	GTAGATAATGTTTAG[C/T]TCAATAAGCAGTTAC	50717
rs568967672	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160237461	CAAAGGACAGTTGAT[C/T]TGCTATTTCAACTAA	50717
rs568985640	snp	G/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160244927	CTAACTTCAAACTTA[G/T]TAAAGGCACAGATAC	50717
rs568989439	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160259205	TCTTCATCTGTGCTG[C/T]CATATTATTAAGACG	50717
rs569153320	snp	C/T	0.00119737	0.0244387	intron-variant	DCAF8	GRCh38.p7	1:160250912	AGGGTCTATGAACAC[C/T]GGTCTGACAACTACC	50717
rs569212150	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160229028	CACATAGCCAGGCGC[A/G]GTGGCTCACGACTGT	50717
rs569396314	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160243533	ATAGGCATGAGCCAC[C/T]ATGCCCAGCCATGTA	50717
rs569416527	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160236103	GGAGCATTTACATTT[C/T]GTCTGTATACTTTAT	50717
rs569452432	snp	A/C	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160226007	CACCACCACGCCCGG[A/C]CAATTTTTGTATTTT	50717
rs569473885	snp	A/G	0	0	intron-variant	DCAF8	GRCh38.p7	1:160225337	CTAGCCATTTTATGT[A/G]CACTGTCTCATTAGG	50717
rs569565411	snp	C/T	6.61299e-05	0.00574983	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240244	CTTTCTGTGCTGGTG[C/T]GGTTGGGGCCACCAT	50717
rs569786630	snp	A/T			intron-variant	DCAF8	GRCh38.p7	1:160227105	GAGGTTCACATAATA[A/T]TTGTACTTCAAGTTA	50717
rs569862259	snp	C/T	0.00119737	0.0244387	intron-variant	DCAF8	GRCh38.p7	1:160255108	TCCAAACATCGTATA[C/T]AATATAGGACACAGT	50717
rs570280726	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	PEA15, DCAF8	GRCh38.p7	1:160215620	ACTTTCTAACACTGT[A/G]TCATGTGCAGAATGA	50717
rs570296731	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160247111	CACTATTTTTACTTT[A/G]ATCAACTTTCATGTA	50717
rs570347241	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160232975	AGATCTAAGCATTCA[A/G]TTAGTCAAATATGAC	50717
rs570359442	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160254263	GAAGGCAGAGGTTGC[A/G]ATGAGCCAAGATTGT	50717
rs570383662	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	DCAF8	GRCh38.p7	1:160239178	ACCAGTACAGTAGAT[A/G]GGGCCAAGGAGTAAA	50717
rs570423484	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160253869	TAAGGAGGATAGTCC[A/G]TGCTTCCAAAAAAAT	50717
rs570505885	snp	C/T			upstream-variant-2KB	DCAF8	GRCh38.p7	1:160263107	CCTACAGTAACCCTG[C/T]AGAGGATTACTCCCA	50717
rs570536157	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239474	ATTTAATAAGCTGCA[C/T]GCACCCTACCTATGA	50717
rs570543933	snp	C/T	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240090	CCGAGGCTGCTCTTC[C/T]TCCTCCTCTTCTTCC	50717
rs570679187	snp	A/G	1.65195e-05	0.00287393	intron-variant	DCAF8	GRCh38.p7	1:160218836	AAAATAACTTCTGCA[A/G]TCAGCCACTTACATC	50717
rs570742687	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160219508	AGGCTGAGTTGCAGG[A/G]AGTGGTGGGAGTGAT	50717
rs570792513	snp	A/T	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160259862	AATACATTTTGAAAT[A/T]TACATACACCAATAT	50717
rs570797602	snp	A/G	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160260697	TTCAGACCAGCTACA[A/G]AAGAAAGAGCAGCCA	50717
rs570862156	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160226977	ATTAGATCTCCAAGG[A/G]AAAATACAGAGAAGA	50717
rs571080188	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160222369	TTTGGAAAAGGTGCA[C/T]GTCTAGAGATAAGTT	50717
rs571081679	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160238246	GCAGGTAAGCTGAAG[C/T]TCTCACACAAGAGGA	50717
rs571141322	snp	A/C	0.00119737	0.0244387	intron-variant	DCAF8	GRCh38.p7	1:160222996	CTGCAGTCCTTTAGC[A/C]GCAGCCTTAGTCTCT	50717
rs571161821	in-del	-/G	0.00279162	0.0372561	utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160217099	GGGGTTGCTGGGGGT[-/G]GGGGGGGGAGCCAAC	50717
rs571276680	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160236322	TATATACGTGTGTGT[A/G]TATAAATACATATGT	50717
rs571407952	snp	G/T	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160235142	GTTATAATAATTTTG[G/T]TTTTTTTTTTTGAGA	50717
rs571419613	in-del	-/AT	0.00159617	0.0282053	intron-variant	DCAF8	GRCh38.p7	1:160245653	GGCAACAAAAAACAG[-/AT]ATGTGAAGCAACATG	50717
rs571489910	in-del	-/T			intron-variant	DCAF8	GRCh38.p7	1:160237757	TTGCCCAGGCTGGTC[-/T]TTTAACTGCTGGCCT	50717
rs571587026	snp	C/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160242294	GTATAAAACAACTGG[C/G]CTAGGGGCTGGAAGA	50717
rs571630242	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160253474	CCAACATGGTGAAAC[C/G]CTGTCTCTACTAAAA	50717
rs571715438	snp	C/G	0.00199481	0.0315187	intron-variant	DCAF8	GRCh38.p7	1:160248443	CCTTTAAAACTGTCG[C/G]AACAGGCTGGGGCTG	50717
rs571722736	snp	A/T	0.00119737	0.0244387	upstream-variant-2KB	DCAF8	GRCh38.p7	1:160263327	GCCAGAGTGCTTTTT[A/T]AAAATGTAAGGTCTG	50717
rs571775760	snp	G/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160248010	TGGATTTATCAAAAT[G/T]AATAAATTCTGATAA	50717
rs571845932	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	DCAF8	GRCh38.p7	1:160262585	AGCTCACGGCTCGCA[A/G]CCCTCCTCGAAGGAC	50717
rs571869268	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	DCAF8	GRCh38.p7	1:160262238	AACCGGCTGGGAAGC[A/G]AGGGGGGGCGCAGGC	50717
rs571974410	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160248163	AATACAAAAATTAGC[C/T]GGGCGTGGTGGCACA	50717
rs572036373	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	DCAF8	GRCh38.p7	1:160262858	TTGCCACAAGGATTT[C/T]TTCTGAAAATCCCCG	50717
rs572087758	snp	G/T	0.00557542	0.0525036	intron-variant	DCAF8	GRCh38.p7	1:160231941	CATGCCTGTAATCCC[G/T]ACACTTTGGGAGACT	50717
rs572114466	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160231763	AGACAATACTACAGA[C/T]ACCTTCCTACCCTTT	50717
rs572248883	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160218222	GTGGATAGGAAATCC[A/G]ACCAAGATCACCTGA	50717
rs572313796	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160260608	CTGCATTTATAAGTA[C/T]GTTCTGACTCCCTTT	50717
rs572379364	snp	C/T	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160219094	GCTGGGGAAGGGAGG[C/T]CCACCCATCCTGAGC	50717
rs572429631	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160258685	AGCTACTCAGCTGAG[A/G]TGGGAAGATCACTTG	50717
rs572474648	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160244657	GAGTCTCATTCTGTC[A/G]CCCAGGCTGGAATGC	50717
rs572486630	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160228640	GGCCACAGGCCAAAA[A/G]GCATGTCTCCCCAGA	50717
rs572508000	snp	A/G	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160246678	AGGTGTCAAGTATAG[A/G]AGCCACTGAAAAATC	50717
rs572525144	snp	A/T			utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160216767	TTTTTAATATATTTA[A/T]AGATATAAAATTAGG	50717
rs572593106	snp	A/G	0.00438332	0.0466095	intron-variant	DCAF8	GRCh38.p7	1:160235509	AATAAACTGTGGTAC[A/G]CCAATGCTATGACAT	50717
rs572649716	snp	G/T			intron-variant	DCAF8	GRCh38.p7	1:160225314	TTCTTTTGGTTGTCA[G/T]CCATGTGCTAGCCAT	50717
rs572658998	in-del	-/C	0.00318978	0.0398085	intron-variant	DCAF8	GRCh38.p7	1:160243877	TCTCTCCACTAAAAT[-/C]CAGGCCTCCACTCTA	50717
rs572704235	snp	C/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160260926	TGACAACAGGATGAA[C/G]AGAACTCAGGCAAAC	50717
rs572706465	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160253416	ACTTTGGGAGGCTGA[A/G]GCGGGTGGATCACCT	50717
rs572755749	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160254257	AAACTGGAAGGCAGA[A/G]GTTGCAATGAGCCAA	50717
rs572766420	snp	A/C	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160260166	CTTTAAATAGATTCC[A/C]TATAATACTAACAAT	50717
rs573011158	snp	A/C/T	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160225493	TCCAGATGACTGACT[A/C/T]GAAAGTCCAAGCTCT	50717
rs573108947	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160257722	CACTGGAACTGATTC[C/T]TTTTTTTGAGACTAG	50717
rs573173224	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160257223	CCTGTGTTCCAAATA[A/G]GTGAGGGTAAACAGC	50717
rs573188417	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160258665	TGATATGCCCCTGCG[A/G]TCCCAGCTACTCAGC	50717
rs573204458	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160248643	GGGAGGAGGAGGTTG[C/T]AGTGAGCTGCGATCG	50717
rs573280407	snp	A/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160235480	CTAGATATCTATCAA[A/T]AAGGTAAAGGTTAAA	50717
rs573287530	snp	A/G	0.00159617	0.0282053	intron-variant	DCAF8	GRCh38.p7	1:160236314	TACATACATATATAC[A/G]TGTGTGTATATAAAT	50717
rs573295388	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160216585	CCTAAAACCTAAAGG[A/G]TAAGTCCCAATCTCT	50717
rs573328820	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160227168	AAGACTGAGCTACTG[A/G]AGAACATCAGCATTT	50717
rs573337364	snp	A/C	0.00199481	0.0315187	intron-variant	DCAF8	GRCh38.p7	1:160234890	GTCCTCTTGAAGGTT[A/C]TATAAACAAGCAACA	50717
rs573486981	snp	C/T	0.00199481	0.0315187	intron-variant	DCAF8	GRCh38.p7	1:160241431	AAAGCTGGGCTACTA[C/T]AGTGGTGCCTAAGAC	50717
rs573508917	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160230587	AGTTCACACTAAGTG[C/T]TCCCAAGTCAAACTA	50717
rs573557359	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160243482	CTCCTGGGCTCAAGC[A/G]ATCTGCCTGTCTCAG	50717
rs573656567	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160249403	ACTGTTACTAGAAAT[A/G]CAAAACAGTACAGTT	50717
rs573663159	snp	C/T			upstream-variant-2KB	DCAF8	GRCh38.p7	1:160263781	AGGACCCTACATGAT[C/T]TGATCTAGCACCTGC	50717
rs573666773	snp	G/T	0.00279162	0.0372561	intron-variant	DCAF8	GRCh38.p7	1:160219900	GAAAAGAGGAACACA[G/T]AGGAAAGGCACCCTG	50717
rs573805968	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160229037	AGGCGCGGTGGCTCA[C/T]GACTGTAATCCCAGC	50717
rs573889469	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160241143	GGCGACAAAGCGAGA[C/T]TCCATCTCAAAAAAA	50717
rs573975324	snp	A/C/G	0.000399281	0.0141238	upstream-variant-2KB	DCAF8	GRCh38.p7	1:160263778	AGGAGGACCCTACAT[A/C/G]ATCTGATCTAGCACC	50717
rs573976457	snp	A/G	0.00119737	0.0244387	intron-variant	DCAF8	GRCh38.p7	1:160229359	ATAGAGGAATATTGA[A/G]GCTGATAAGACACAG	50717
rs574193568	snp	C/T	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160248112	GGAGTTCGAGATCAG[C/T]CTGGCCAACATGGTG	50717
rs574195093	snp	A/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160233874	GGTGCTATAAAAATG[A/T]TTATCATGGCAATAG	50717
rs574195422	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160242005	CCCAGCGCTTTGGGA[A/G]GCCAAGGCGGGTGGA	50717
rs574199933	snp	C/T	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160222027	CAATTGCCACATTTG[C/T]GTTCTCCTTATATGT	50717
rs574260881	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160241314	GTAAATATATTTTGA[C/T]TTACTTCCATTAGTT	50717
rs574321592	snp	C/T	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160240676	TTGTATAAAAGTGTG[C/T]CTGATACATCTACCA	50717
rs574388528	snp	C/T			downstream-variant-500B	PEA15, DCAF8	GRCh38.p7	1:160215565	TCCAACAGTCTCCAA[C/T]TGGAGCCCAAGCACT	50717
rs574449541	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160252449	ATTCCACAGGACCAG[A/G]GCAAGAAAAGATATG	50717
rs574536418	snp	C/T	0.00279162	0.0372561	intron-variant	DCAF8	GRCh38.p7	1:160230884	AGCCTCTTGAGCAGC[C/T]GGGACTACACGCATG	50717
rs574657084	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160226301	TTAAAACTGTATTTG[A/G]CCTGTTCTCCCTCTC	50717
rs574711702	snp	G/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160251395	TTTATTTTACTTTTC[G/T]TAATATTTCTCCTTC	50717
rs574938261	snp	C/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160248442	TCCTTTAAAACTGTC[C/G]CAACAGGCTGGGGCT	50717
rs574941852	snp	A/T			intron-variant	DCAF8	GRCh38.p7	1:160248825	CTTAAGTCTAGGAGT[A/T]CAAGGCTGCAGTGAG	50717
rs575002696	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160244955	TACTAAGGATTATAG[A/G]GCTGAAACTAGAAAT	50717
rs575163031	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160230038	AAAAAAAAAAATCTA[C/T]GGCTACACATTTAAG	50717
rs575171011	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160222483	GGAACAGGAAGAAAA[C/T]ACTCCATCAAAAACT	50717
rs575276890	in-del	-/AT	0.00767743	0.0614798	intron-variant	DCAF8	GRCh38.p7	1:160236332	TGTGTATATAAATAC[-/AT]ATGTGTGTATATGTG	50717
rs575357453	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160237725	TTGTTTGTTTTCCAC[A/G]GATGGGGTCTTGCTA	50717
rs575423211	snp	A/C	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160236672	TAAAATTTACCTATG[A/C]GTCTCAGATTCACAT	50717
rs575430589	snp	G/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160251206	CACACAGTCCCAAGT[G/T]TCTCTTGGGAGGACA	50717
rs575543901	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160242729	TCAACTCCAGTATGT[A/G]GAACAAAAGCAACTC	50717
rs575544938	snp	A/G	0.000181598	0.00952711	intron-variant	DCAF8	GRCh38.p7	1:160243918	AGGAGGACAACCTCA[A/G]TTGATAGTAAAAATA	50717
rs575599135	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	DCAF8	GRCh38.p7	1:160262698	AGTTTCTTCGGGCTT[C/G]CTTATCTTGTGATAC	50717
rs575662464	snp	G/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160261987	GGCCCTGAGGTGACG[G/T]GGAGACGCAGGGCGA	50717
rs575707226	snp	G/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160223615	CTGTTATTTTTAAAA[G/T]AACACCAGGATTGGG	50717
rs575733499	snp	A/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160227284	TAATAATGTCAAGAG[A/T]AGAGAAAAAGACTTG	50717
rs575819271	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160232370	ATAAAAAGCCGGGTG[C/T]GGTGGCTCACGCCTG	50717
rs575882584	snp	C/G	0.000399281	0.0141238	downstream-variant-500B	PEA15, DCAF8	GRCh38.p7	1:160215487	GGGAAAATACCCCAA[C/G]TGTATACCCTCACCC	50717
rs575943835	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239534	TCTAGGGTTGCCAAG[A/G]GTCTTTCAGTGTATT	50717
rs575947248	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160216355	TCACAAAGTACCACA[A/G]TAGTCTGCAGTGGTG	50717
rs576236706	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160231718	CTCAGTTTAGCTGCA[A/G]TCCAACACAGTAACA	50717
rs576346423	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160219811	CTTCCCTAAGGGAAG[A/G]GCAGGGAAGTTCCTA	50717
rs576546424	snp	A/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160259902	TCTGTCCTCTGGTTA[A/T]GAACCCCCACCAAGG	50717
rs576589624	snp	C/T	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160259370	AAACCCCTCCTCTAC[C/T]AAAAATACAAAAATT	50717
rs576603501	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160241070	GGCAGTAGAATGGCA[C/T]GAACCCAGGAGGCAG	50717
rs576621151	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160260187	TACTAACAATGACCC[C/T]GGGAGGTAAGTGGTA	50717
rs576692648	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160223898	TGCACTCCAGCCTGG[A/G]CAACAGAGTGAGATC	50717
rs576716300	in-del	-/T			intron-variant	DCAF8	GRCh38.p7	1:160251105	CTACATAAACACCCA[-/T]TATTTAAATGAGACA	50717
rs576729897	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160260984	AATATGATCGACACA[A/G]AGACAAAATACAAGG	50717
rs576742715	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160224366	GGTAGTTTCTATTTG[C/T]ATAACCTGAGTAAGA	50717
rs576758060	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160218972	AAGACAGTTTACCTG[A/G]TCAGGAAGAAAGGAA	50717
rs576797613	snp	C/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160253140	AGAGAAAGGAGAGCA[C/G]AGAGAAAAATTGAGA	50717
rs576871372	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160217841	GCCAGAGAGTAAATA[C/T]TTTAGACTTGTGGTC	50717
rs576951023	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160231093	ATAATCTCTAAAATA[C/T]GTAAAGTCACCCCTC	50717
rs577012239	snp	C/T	0.000399281	0.0141238	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160238717	CACACATGGCCAGAG[C/T]AGAATCACCACTGTT	50717
rs577072189	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160237847	ACCCAGCAACAGTTC[A/G]TTCTCGAATAAAATC	50717
rs577137714	snp	G/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160229173	AAGTGGCACATGCCT[G/T]TAATCCCAGCTACTT	50717
rs577147958	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160225523	TTCCCACCATACCAA[C/T]AAGTTCAGGTGCAGC	50717
rs577260765	in-del	-/AAAAAAAAAAAAAA	0.41833	0.184838	intron-variant	DCAF8	GRCh38.p7	1:160221818	CTAATTCTAGGTCTC[-/AAAAAAAAAAAAAA]AAAAAAAAAGATAAG	50717
rs577262393	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160220894	CCCACTGCTGGAAAA[C/T]TAGGACCAAAAAACA	50717
rs577267101	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160259304	CTTTGGGAGGCTGAG[A/G]CGGGCAGATCACAAG	50717
rs577472628	snp	A/G	0.00597247	0.0543191	intron-variant	DCAF8	GRCh38.p7	1:160243282	TCCTGAAAAGAAGGA[A/G]GAGGGAAAGGAAGGA	50717
rs577542920	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160252828	AAGTTCTTAGTCTGG[C/T]GCCCAGAGAAAATCA	50717
rs577663155	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160256383	ACATTAAAGAGAGGC[C/T]TAAAACCTCAAGAAG	50717
rs577720754	snp	A/C/T	0.000399281	0.0141238	upstream-variant-2KB	DCAF8	GRCh38.p7	1:160263592	GCAGTGAGCTGAGAT[A/C/T]GCACCACTGCACTCC	50717
rs577886969	snp	A/C	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160224204	AAACAGTTAGTCTAG[A/C]CTCCTTATGTCCAAA	50717
rs577896452	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160240545	AATCTTGTAAAGGAC[A/G]AGAAATTGAAAAGAT	50717
rs577920692	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160230483	ATGTCTCAAGAGCCA[A/G]TGTTAACAAAAGGTG	50717
rs577959110	in-del	-/AT	0.00159617	0.0282053	intron-variant	DCAF8	GRCh38.p7	1:160236372	TGTGTGTATATAAAC[-/AT]ATATGTGTGTGTATA	50717
rs578104706	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160241025	AAAAATTAGCCGGGC[A/G]CCTGTAGTCCCAGCT	50717
rs578186624	snp	A/G	0.000798403	0.0199641	intron-variant	DCAF8	GRCh38.p7	1:160261841	TAGAGGAGGTAAACT[A/G]AGATAATTATATTAC	50717
rs578202487	snp	A/C/G	0.00016513	0.00908522	intron-variant	DCAF8	GRCh38.p7	1:160222814	GGAAGAAACCACATG[A/C/G]GGGTTGGCATCAGGC	50717
rs578235665	snp	A/C	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160223437	CTCTAACTGCTATCT[A/C]CAAGACAAAATCATG	50717
rs578249987	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF8	GRCh38.p7	1:160254098	GGAGGCCGAGGCAGG[C/T]GGATCATGAGGTCAG	50717
rs578251439	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PEA15, DCAF8	GRCh38.p7	1:160215345	GCCTTGTTCTAACCC[A/G]GAATAAAGGTGATTG	50717
rs587777425	snp	A/G	1.67925e-05	0.00289758	DCAF8	1	allele_origin=G(germline)/A(germline)	1:160237145	CTTACGACGCTGGGC[A/G]GTCTTGTCTCAGGTC	50717
rs745317914	snp	A/G	1.64741e-05	0.00286998	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160218335	TTACCCGGTGATGGC[A/G]TCTCTGTCTCAGGTG	50717
rs745334092	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160224212	AGTCTAGCCTCCTTA[C/T]GTCCAAACCAATTAG	50717
rs745438760	snp	A/G			upstream-variant-2KB	DCAF8	GRCh38.p7	1:160262647	AACAGAGCGAGAGGC[A/G]CCTGCGCATTACCGA	50717
rs745507749	snp	C/T	1.65195e-05	0.00287393	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160217707	CCAGGTTCTCGCCAG[C/T]GCTGTGGATGGGAAA	50717
rs745520689	snp	C/T	3.50349e-05	0.00418524	intron-variant	DCAF8	GRCh38.p7	1:160238569	GAGAACCACAGAGGA[C/T]TTGGATTGCACAAAT	50717
rs745523906	snp	A/T			intron-variant	DCAF8	GRCh38.p7	1:160247574	GTATCCTCTTACCCA[A/T]AATGCTTGGGGCCAG	50717
rs745547104	snp	C/T	6.64849e-05	0.00576524	intron-variant	DCAF8	GRCh38.p7	1:160231443	AGAAAGTTATATACT[C/T]CAAAAGATCCAAATG	50717
rs745554133	snp	A/G	0.000189018	0.00971974	upstream-variant-2KB	DCAF8	GRCh38.p7	1:160263253	CTTAAGACTACCGCA[A/G]TAGAAACTTACCTCG	50717
rs745591149	snp	A/C	1.65751e-05	0.00287876	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160225117	TTTGGACTCACTGTT[A/C]ACCTGCAATAAGGAG	50717
rs745596263	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160232305	TGAGGCTAGGAGCTC[A/C]AGATCACCCTGGGCA	50717
rs745611838	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160248979	GGCAGATCACCTGAG[A/G]TCAGGAATTTGAGGC	50717
rs745698198	in-del	-/G	1.67815e-05	0.00289663	intron-variant	DCAF8	GRCh38.p7	1:160224598	AGGCTGAAAAAAGCA[-/G]GGACCAGGAGGTGGG	50717
rs745776382	in-del	-/TCCTCT	0.0143877	0.0835874	cds-indel, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240106	TCCTCCTCTTCTTCC[-/TCCTCT]TCCTCTTCCTCTGAG	50717
rs745787256	snp	A/C	1.64792e-05	0.00287042	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240017	CCCAGTCCTCTAGGG[A/C]CCGCTCATCATCTGA	50717
rs745800919	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160219198	CTATGTATAGGTCGG[A/G]GGTGGCTTCATCCCC	50717
rs745845817	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160256609	CGTGAGGCAAATATG[C/T]ATGCTTCACTTTAGA	50717
rs745852944	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160240739	AGTTATAGCAAATAA[C/T]TAAACAGAATATAAA	50717
rs745912703	snp	A/C/T			intron-variant	DCAF8	GRCh38.p7	1:160258044	CCTGGCAGATTCTTA[A/C/T]ACATTTAATTGACTG	50717
rs746101275	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160227319	GTACTTTGTTTGCTT[C/T]GGCAGTTAGGTTACT	50717
rs746106937	in-del	-/TA			intron-variant	DCAF8	GRCh38.p7	1:160236448	GTGTGTGTGTGTGTA[-/TA]TATATATATATATCC	50717
rs746113813	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160244244	TATAATGATATATTT[C/T]TGGGGAGGTCAAGTG	50717
rs746124785	snp	C/T	3.30322e-05	0.00406387	intron-variant	DCAF8	GRCh38.p7	1:160225576	CTGCAGCAACTGGCC[C/T]TTCATGAATCTTACC	50717
rs746187993	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160229027	TCACATAGCCAGGCG[A/C]GGTGGCTCACGACTG	50717
rs746244662	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160225277	GAAACATGACCACCT[A/C]AGGGGGTAGCATCTT	50717
rs746284391	snp	C/T	1.64746e-05	0.00287002	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160222687	CATGAACTGAATAAT[C/T]TGGCAGGATGATTTC	50717
rs746288912	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160251458	CCTTCCACACTCTAA[C/T]AGCATAGTGGTTTTG	50717
rs746363191	snp	A/C	1.65359e-05	0.00287536	intron-variant	DCAF8	GRCh38.p7	1:160218992	GAAGAAAGGAAAACA[A/C]AGACTCAGCAGTGTG	50717
rs746378683	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160252654	GAAAAGGAAAGAGAA[A/G]CAAGTTTAAAAGCTA	50717
rs746420106	snp	A/G	3.51475e-05	0.00419196	intron-variant, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239602	ATATGTAATTCCTAC[A/G]ATAACTCACTATCAG	50717
rs746477428	snp	A/C	1.648e-05	0.0028705	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240029	GGGCCCGCTCATCAT[A/C]TGATGAGTCCTGGTC	50717
rs746479342	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160237593	GTGCAGTGGCATGAT[C/T]ATGGCTCACTAAAGC	50717
rs746668609	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160261140	CTTGTAAAAGTAATT[C/T]AACCAGAGCTGGAAC	50717
rs746687484	snp	A/C	1.70685e-05	0.00292129	missense, nc-transcript-variant, downstream-variant-500B	DCAF8	GRCh38.p7	1:160238726	CCAGAGTAGAATCAC[A/C]ACTGTTAGGAAGAAA	50717
rs746755288	snp	A/T	1.65255e-05	0.00287445	intron-variant	DCAF8	GRCh38.p7	1:160231246	CACCTGGTAGTATAC[A/T]ATGCATCAGTCTTAC	50717
rs746756298	snp	G/T			intron-variant	DCAF8	GRCh38.p7	1:160246217	AGAACAGATCTGATG[G/T]TTTCCCACCTCCATA	50717
rs746783575	in-del	-/CTC	1.66183e-05	0.00288251	cds-indel, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240345	TTCAGCTCCAGACAT[-/CTC]CTCTGGACTGCTAGA	50717
rs746794374	snp	A/G			utr-variant-5-prime, upstream-variant-2KB	DCAF8	GRCh38.p7	1:160262543	CGACGATGTGCTCGA[A/G]AAGACTGAGGGAAGA	50717
rs746865442	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160230694	ATATAGTACTTGCTG[A/G]TAAACCTAAATTTAT	50717
rs746909756	snp	C/T	3.2993e-05	0.00406145	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160225625	TTCTTGAGTACTCCA[C/T]TGTTCTCATTCTCAT	50717
rs747003693	snp	C/T	1.65985e-05	0.00288079	intron-variant	DCAF8	GRCh38.p7	1:160219014	AGCAGTGTGTGGGAG[C/T]AGGGTTTAAAAACCA	50717
rs747023858	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160231962	TTGGGAGACTGAGGC[A/G]GGTGGGTCACTTGAG	50717
rs747132903	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160218676	TAGTGCCACTTCACA[A/G]CTGCCCCCTGGAGCA	50717
rs747211563	in-del	-/AA			intron-variant	DCAF8	GRCh38.p7	1:160253647	GTGAGACTCCATCTC[-/AA]AAAAAAAAAAAAAAA	50717
rs747227497	snp	C/G	1.7251e-05	0.00293687	intron-variant, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239615	ACAATAACTCACTAT[C/G]AGCTCCCAATCCATG	50717
rs747279847	snp	A/C	1.64743e-05	0.00287	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160243984	AGTCTGTTCTGCCAT[A/C]TGTGCTGCTCCCTTT	50717
rs747332040	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160256474	CAAAACATACCTGGT[A/C]ATGTGGCAATCATTA	50717
rs747389159	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160252746	AAAAGGGATCAACAT[A/G]AGAATCGTTGTAAAG	50717
rs747479876	snp	A/T			intron-variant	DCAF8	GRCh38.p7	1:160249349	AAAATTTACTTTATT[A/T]AGTACTAACAAGAAG	50717
rs747563431	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160224055	CCTCATCTAAAAGAA[C/T]TGTTTACTCCTCCTT	50717
rs747596769	in-del	-/AG			intron-variant	DCAF8	GRCh38.p7	1:160253887	CTTCCAAAAAAATAC[-/AG]AGAACAGTATACTGT	50717
rs747640326	snp	A/G	1.67156e-05	0.00289093	intron-variant	DCAF8	GRCh38.p7	1:160225666	CTGGTCATAAATCCT[A/G]CAGTTGGAAAAGCAA	50717
rs747648718	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160251263	CAGCTGTTCAGGGTT[C/G]ATCTCCATCCAAAGT	50717
rs747736198	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160236319	ACATATATACGTGTG[C/T]GTATATAAATACATA	50717
rs747785917	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160220793	GTTCTAACATTCTAC[A/G]TTACAATTACATTCT	50717
rs747789970	snp	C/G	3.33907e-05	0.00408586	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240131	CTTCCTCTGAGCGGT[C/G]ATGGACTCGATTTTC	50717
rs747821635	snp	A/T	1.65162e-05	0.00287365	intron-variant	DCAF8	GRCh38.p7	1:160218983	CCTGGTCAGGAAGAA[A/T]GGAAAACACAGACTC	50717
rs747897875	snp	G/T			intron-variant	DCAF8	GRCh38.p7	1:160222379	GTGCACGTCTAGAGA[G/T]AAGTTACATCACTCA	50717
rs747933650	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160246572	GGCTGAGAAAGGACT[A/G]CTTGAGCTCAGGAAT	50717
rs748026533	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160244572	GGGGAAGAGATTGAG[C/G]TTTCTGTTCACTCAG	50717
rs748037344	snp	A/G	8.24545e-05	0.00642032	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160217660	CTGAGGAGCTGGGAG[A/G]CTCATCAGAGTCCGC	50717
rs748045176	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160261080	ATTTGGAGATACACA[A/G]CAATAGTTTAGGACA	50717
rs748062698	snp	C/T	1.65266e-05	0.00287455	intron-variant	DCAF8	GRCh38.p7	1:160231256	TATACAATGCATCAG[C/T]CTTACAAACTGTCAA	50717
rs748162409	snp	C/T	1.64895e-05	0.00287132	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160224478	CCTTGTATCTCTTAA[C/T]ATACTGGGCCCCATC	50717
rs748200275	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160230553	GGTAGCTCAGGACAG[C/T]GAGAGCCAAAAAACC	50717
rs748226233	snp	A/T			downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	PEA15, DCAF8	GRCh38.p7	1:160215822	AGGAACACAGACCAC[A/T]CGATCACCACACATT	50717
rs748358744	snp	A/G	0.00011532	0.00759255	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160222735	CCCACAGTCACTACC[A/G]CTCACCACAAACTCA	50717
rs748364054	in-del	-/AG			intron-variant	DCAF8	GRCh38.p7	1:160248291	CAGCCTGAGTGACAA[-/AG]AGAGACTCCATCTAG	50717
rs748374917	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160254125	TCAGGAGTTTGAGAC[C/G]AGCCTGGCCAACATG	50717
rs748398683	snp	C/G/T			utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160217100	GGGGTTGCTGGGGGT[C/G/T]GGGGGGGAGCCAACT	50717
rs748439701	snp	G/T	3.33078e-05	0.00408078	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239751	TACTGGCTGCCGCCG[G/T]ACCCAATCCCACACC	50717
rs748466926	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160255909	ACAGATGTAAGCCAC[C/T]GTGCATGGCCTCTGG	50717
rs748502215	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160240721	TTGGATGGGCATTTA[C/T]TAAGTTATAGCAAAT	50717
rs748566176	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160224319	CCAGCCCAATTCAGG[A/G]TAATCCCTCAGTGCC	50717
rs748591910	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160225913	CAGTGGCATGACCCC[A/G]GCTCACTGCAACCTC	50717
rs748640166	in-del	-/T			intron-variant	DCAF8	GRCh38.p7	1:160222270	AGCCAAGATCACTAC[-/T]TTAGTTTAGTTTAAA	50717
rs748657772	snp	C/G	0.000325998	0.012763	upstream-variant-2KB	DCAF8	GRCh38.p7	1:160263405	GATGTGGGCGGATCA[C/G]TTGAGGTCAGGAGTT	50717
rs748702580	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160226005	CACACCACCACGCCC[A/G]GCCAATTTTTGTATT	50717
rs748712978	snp	C/G	1.64762e-05	0.00287016	utr-variant-5-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160244031	GATGTTTGCTGTAGC[C/G]AGCCTGGGTTTGGGA	50717
rs748728412	snp	G/T	1.65296e-05	0.00287481	intron-variant	DCAF8	GRCh38.p7	1:160231424	TTTAAGAGTAGAAAA[G/T]CACAGAAAGTTATAT	50717
rs748811621	snp	C/T			upstream-variant-2KB	DCAF8	GRCh38.p7	1:160264141	TCTTGAGGGCAAGGA[C/T]TGTGTTTTTATCATC	50717
rs748817558	in-del	-/AAAT			intron-variant	DCAF8	GRCh38.p7	1:160258344	GAGATCCTATTTCAA[-/AAAT]AAATAAATAGACTGC	50717
rs748852322	in-del	-/AG			intron-variant	DCAF8	GRCh38.p7	1:160249521	TTTATACAAGAAAAA[-/AG]AGGCTCAGACCTGTT	50717
rs748865268	snp	A/T			intron-variant	DCAF8	GRCh38.p7	1:160249013	CCTGACCAACGTGGT[A/T]AAACCCCATCTCTAT	50717
rs748896523	in-del	-/CATATGAATA			intron-variant	DCAF8	GRCh38.p7	1:160229478	ATATGATATACATAT[-/CATATGAATA]CATATGAATACATAC	50717
rs748922820	snp	C/T	1.6476e-05	0.00287014	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160231309	CACCTTACAAACTGA[C/T]CTCGTCCACCCACTG	50717
rs748935643	snp	C/T	1.65825e-05	0.00287941	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240335	CCCTCCCCTCTTCAG[C/T]TCCAGACATCTCCTC	50717
rs748958830	snp	A/G	1.64833e-05	0.00287078	intron-variant	DCAF8	GRCh38.p7	1:160243945	AATAGCTTCACCTTC[A/G]TTTTGGCCCCTTACC	50717
rs749000600	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160219414	GCAGCTGCCAATGAA[C/T]CCCCAGAGAAGAGTC	50717
rs749030701	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160228735	GAGGATCAGTAAGCT[A/G]TTTCTCTATATTCCC	50717
rs749036129	snp	A/G	1.6477e-05	0.00287024	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239853	ACCAGTATGGCCCTC[A/G]AGCCCATGCTGCAGG	50717
rs749045507	in-del	-/AAGG			intron-variant	DCAF8	GRCh38.p7	1:160243288	AAGAAGGAGGAGGGA[-/AAGG]AAGGAAGGAAGGAAG	50717
rs749147795	in-del	-/TTATT			intron-variant	DCAF8	GRCh38.p7	1:160235030	TAATCAGCCTTCATG[-/TTATT]TTATATTCCCCAATA	50717
rs749151838	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160258267	TGGGAGAATCACCTA[A/G]GCCCAAGAGGTCGAG	50717
rs749158270	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160220745	TCAGTCAGGAGATCT[A/G]GGCAAGGCAGAAAAT	50717
rs749238271	in-del	-/G	8.24015e-05	0.00641825	intron-variant	DCAF8	GRCh38.p7	1:160218465	AAAAGGTTGGGAAGA[-/G]GGGGGCAGCAATGAA	50717
rs749242987	snp	A/T			intron-variant	DCAF8	GRCh38.p7	1:160259284	TCACACCTGTAATCC[A/T]AGCACTTTGGGAGGC	50717
rs749246390	snp	A/G	3.29745e-05	0.00406031	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160217676	CTCATCAGAGTCCGC[A/G]TCTGTGGCCCCAACC	50717
rs749280662	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160244437	GGCAAGAATCTTCCA[A/G]TGTAAATAAGTGACA	50717
rs749369831	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160229162	ATAGCCAGGCAAAGT[A/G]GCACATGCCTGTAAT	50717
rs749447355	snp	A/G	1.65012e-05	0.00287234	intron-variant	DCAF8	GRCh38.p7	1:160225058	CTGGGCCCTGCTCAC[A/G]TACCTGTGCCGTCGT	50717
rs749593199	snp	A/G	1.65905e-05	0.0028801	intron-variant	DCAF8	GRCh38.p7	1:160218819	TGTGGATAAGCAGAA[A/G]GAAAATAACTTCTGC	50717
rs749639727	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160252766	TCGTTGTAAAGGTAG[A/G]TAATGTTTAGCTCAA	50717
rs749823037	snp	G/T			intron-variant	DCAF8	GRCh38.p7	1:160223213	GTATATGCCACAACT[G/T]CCTCGAGAAGCAAGT	50717
rs749829097	snp	A/G			intron-variant, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239230	TATAAGCTAACATTT[A/G]TCAAATGTTTATTAA	50717
rs749829107	in-del	-/TGACT			utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160215974	TGATTTAGAAGAATC[-/TGACT]GTCCCAGGATACAGA	50717
rs749834716	snp	A/C	1.67857e-05	0.00289699	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160238693	CTACTCGAACCTGCC[A/C]GTCACGGGCACACAT	50717
rs749847767	snp	A/G/T	0.000293293	0.0121068	intron-variant	DCAF8	GRCh38.p7	1:160238596	AAATTTTGGAGCAAG[A/G/T]TCTTACTTACCTTGT	50717
rs749916823	snp	C/T			missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240262	TTGGGGCCACCATCA[C/T]CCCCAGTCAAGCTCA	50717
rs749942748	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160242893	ATAGTATACTTTAAC[C/T]CCTCTAGAACCCTGT	50717
rs750070793	snp	G/T			intron-variant	DCAF8	GRCh38.p7	1:160244242	CATATAATGATATAT[G/T]TTTGGGGAGGTCAAG	50717
rs750184781	snp	C/T	1.65143e-05	0.00287348	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240076	CGCTGTACACGGCGC[C/T]GAGGCTGCTCTTCTT	50717
rs750185035	snp	A/T			intron-variant	DCAF8	GRCh38.p7	1:160227958	GGAGTGCAGTGGTGT[A/T]ATCACAGCTCACTGT	50717
rs750259973	snp	A/T			intron-variant	DCAF8	GRCh38.p7	1:160250858	GCTCTTTATTTTTTT[A/T]AAATTTCTCTGAATT	50717
rs750318477	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160236019	GCTGGGATTACAGGC[A/G]TGAGCCACCGTGCCC	50717
rs750324156	in-del	-/C			intron-variant	DCAF8	GRCh38.p7	1:160244194	CTTGTGAAATTTTTT[-/C]TTCCTTATGTTTTCT	50717
rs750346765	snp	C/T	1.64749e-05	0.00287005	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160218935	CACTGGTTGCCAGCA[C/T]AGGCAGGTGAGGGTG	50717
rs750347768	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160251901	ATTTTCTATTAAGTA[C/T]TTGGAGGGGTCCAAC	50717
rs750393945	snp	C/G	4.15481e-05	0.00455767	intron-variant, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239561	TATTTAGGTCATTAG[C/G]GGAGCCAAAGTAGGG	50717
rs750406641	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160220453	CAAGAGAATAACATA[C/T]AGTACCTGAATTGGA	50717
rs750453364	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160237038	ATAGGCACAAAGGTA[C/T]TATTCGGATGAACCA	50717
rs750541832	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160221961	AAGGCCAGGCAGACT[A/C]TGATACGATCATGGG	50717
rs750582995	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160259202	AACTCTTCATCTGTG[C/T]TGTCATATTATTAAG	50717
rs750591439	in-del	-/T			intron-variant	DCAF8	GRCh38.p7	1:160227734	TGGTCATAAACAACA[-/T]GTAAAGTAAGGCCAT	50717
rs750599788	snp	C/T	8.23635e-05	0.00641677	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160231354	TTGGCAGGATTCACA[C/T]AGATCGTATACAGCC	50717
rs750622814	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160260074	TTATTCAAAGCTGTA[C/T]CAATGATGTGCAAAA	50717
rs750667133	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160251800	TCAGAGAACCTCAGG[A/C]ACTGAAACTCAAAGG	50717
rs750702087	in-del	-/CAAAAAAAAAAAAA			intron-variant	DCAF8	GRCh38.p7	1:160221817	CCTAATTCTAGGTCT[-/CAAAAAAAAAAAAA]AAAAAAAAAAGATAA	50717
rs750731679	snp	A/C	1.65184e-05	0.00287384	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239799	GCTGCCACTGGCCAG[A/C]CAGGTGCCGCGCTGG	50717
rs750754570	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160261513	AACAAATAACCCACA[C/T]ACATATGGAAATAAA	50717
rs750839312	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160230353	GATGAGCCCAAAGAA[A/G]CATAGTTAAAATAGG	50717
rs750873162	snp	C/T	1.65776e-05	0.00287898	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239710	ACCTGGAACACATTA[C/T]TTTTGTGGCCACTCT	50717
rs750893488	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160234683	CTTTTTTGCTCTTCC[C/T]TATGAAAAACTTGCT	50717
rs750923596	in-del	-/CA	1.75742e-05	0.00296425	intron-variant	DCAF8	GRCh38.p7	1:160238560	ACCTTGGCTGAGAAC[-/CA]CAGAGGATTTGGATT	50717
rs750981159	snp	C/T	1.66371e-05	0.00288414	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160217593	CTAGGTATGAGGCCT[C/T]AAGATGGCATGCACT	50717
rs751100608	snp	C/T	1.64846e-05	0.0028709	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160218961	GGGTGGGGCTCAAGA[C/T]AGTTTACCTGGTCAG	50717
rs751152053	snp	C/T			intron-variant, downstream-variant-500B	DCAF8	GRCh38.p7	1:160239168	AATGGCTGGTACCAG[C/T]ACAGTAGATGGGGCC	50717
rs751206825	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160242500	ACACCAAAACATCTA[A/G]TGTTTATTGTTAAAA	50717
rs751240226	snp	A/C/G	1.66203e-05	0.00288268	missense, stop-gained, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240116	CTTCCTCCTCTTCCT[A/C/G]TTCCTCTGAGCGGTC	50717
rs751248301	in-del	-/ACACAT			intron-variant	DCAF8	GRCh38.p7	1:160236272	CACACAAACACACAC[-/ACACAT]ACATACACGTACGTA	50717
rs751298136	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160225372	ACCATCAAGGTGCAA[A/G]GCAGTTATTTTTATT	50717
rs751337542	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160226536	TTCTCACCCAGTCTC[C/T]TCCAATCTCAGAGCC	50717
rs751338030	in-del	-/A			utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160216809	GATAGGGACAGGGAG[-/A]TTGCTGCCACCAAAC	50717
rs751482480	in-del	-/G			intron-variant	DCAF8	GRCh38.p7	1:160221363	GGGGGACCTATGGAA[-/G]AGTTGGAAATGAAGC	50717
rs751525040	snp	A/T	1.65184e-05	0.00287384	intron-variant	DCAF8	GRCh38.p7	1:160222630	ATTAGGGAGCCAGCC[A/T]GCTCAGCACACCATA	50717
rs751617723	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160250631	TGAGAGCATAATGTC[C/G]AGACTTCTCACTTGA	50717
rs751645435	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160234531	AAAGTCATTCGCTCT[A/G]TTCATTACTTGCACC	50717
rs751705612	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160235775	ATGGAGTTTTGCTCC[A/G]TCACTCAGGATGGAG	50717
rs751779094	snp	A/G	8.84682e-05	0.00665028	intron-variant	DCAF8	GRCh38.p7	1:160237121	TTCTGTAATGATATT[A/G]CTGCTACACTTACGA	50717
rs751782671	snp	A/T			intron-variant	DCAF8	GRCh38.p7	1:160257886	CAAGTACTTGCCCCA[A/T]GCTTGGCTTTTTTTT	50717
rs751823172	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160220163	CCCCGTTCTTTATCT[A/C]CTCCTCCCATTCCAC	50717
rs751870443	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160258829	CTGATTTACTACATA[C/T]AGATGTCACCTGGAC	50717
rs751991038	snp	A/G	1.6517e-05	0.00287372	intron-variant	DCAF8	GRCh38.p7	1:160224564	TCTGCCAAGAACAAG[A/G]ACATAGCAGTGAAGG	50717
rs752042764	snp	A/G	1.6819e-05	0.00289987	intron-variant	DCAF8	GRCh38.p7	1:160224416	CAACAGGCTTGGGCC[A/G]AAGAAACCTAGGAAG	50717
rs752052964	snp	C/T			upstream-variant-2KB	DCAF8	GRCh38.p7	1:160264011	ACTAAAATGGAACCT[C/T]ATGTCATCCTCCTCT	50717
rs752089736	snp	C/T	4.94588e-05	0.00497262	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239809	GCCAGCCAGGTGCCG[C/T]GCTGGTTAAAGTGCA	50717
rs752091630	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160228845	TATACCAGAAGATGA[C/G]CTGTTTGGGTTCTTT	50717
rs752108380	in-del	-/G			intron-variant	DCAF8	GRCh38.p7	1:160260808	CAACTAAAGGCAGCA[-/G]TCACTCATCACTCCC	50717
rs752168406	snp	C/T			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PEA15, DCAF8	GRCh38.p7	1:160215294	ATTGCTGTGAGATTG[C/T]CCCTATCTTGTGCTC	50717
rs752213319	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160252415	AGGCAGGATTTCAAC[A/G]GGTAGAGTTGAGAAA	50717
rs752262535	snp	C/G	1.65542e-05	0.00287695	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239791	AGGTCATCGCTGCCA[C/G]TGGCCAGCCAGGTGC	50717
rs752281586	in-del	-/A			intron-variant	DCAF8	GRCh38.p7	1:160230446	GGAGACTGAATCCAC[-/A]AGTGTCTGTTTTCCT	50717
rs752353308	in-del	-/GA	3.81061e-05	0.00436482	intron-variant, downstream-variant-500B	DCAF8	GRCh38.p7	1:160238789	ACACACAAAAGAAAT[-/GA]GAGAGGTAAACTTGA	50717
rs752366102	snp	A/G	1.64795e-05	0.00287045	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160222654	CACCATACTCACCAC[A/G]CCTCCCTTGTCCCCC	50717
rs752392753	snp	C/G			intron-variant, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239413	GAACTCAGGCAGTTT[C/G]GTTCAAGAGCCTGTG	50717
rs752404018	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160253517	GCCACACGCGGTGGC[A/G]TACGCCTGTGATTCC	50717
rs752405257	in-del	-/T			intron-variant	DCAF8	GRCh38.p7	1:160241249	AGCAAGCTGAAGGGG[-/T]TAAGTGGGAATTGTG	50717
rs752414488	in-del	-/T			upstream-variant-2KB	DCAF8	GRCh38.p7	1:160263140	TGCCAGGCTGGGGTA[-/T]TTTTTTTTTTTTTCT	50717
rs752448194	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160235475	ACGATCTAGATATCT[A/G]TCAATAAGGTAAAGG	50717
rs752535523	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160223776	AGAGGCATGCACCTG[C/T]AGTCCCAGCTACTCA	50717
rs752612943	snp	A/T	8.24599e-05	0.00642053	intron-variant	DCAF8	GRCh38.p7	1:160244076	AACAATTAGGAAACC[A/T]CCTGGGAAAGAAGAC	50717
rs752625360	snp	A/C			missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160225082	CCGTCGTGGCTGTAC[A/C]CAAGACAGGTGATGT	50717
rs752665639	snp	C/G			utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160216362	GTACCACAATAGTCT[C/G]CAGTGGTGGCACCAC	50717
rs752666422	snp	C/T	3.30136e-05	0.00406273	intron-variant	DCAF8	GRCh38.p7	1:160243919	GGAGGACAACCTCAG[C/T]TGATAGTAAAAATAG	50717
rs752759630	snp	A/G	1.64773e-05	0.00287026	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239978	GCCAGCGAGGTCGGG[A/G]TAGAGCTGATGTTTC	50717
rs752778861	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160256206	TCAGTTTAACTAATT[A/C]CTAGGGAAATCTACT	50717
rs752873519	snp	C/T	1.64817e-05	0.00287064	intron-variant	DCAF8	GRCh38.p7	1:160218296	AAAGGGTCACTCCCT[C/T]GGGAATTCATTTCCA	50717
rs752875193	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160231874	GACCTTAAGGTCAGA[C/G]ACTATTGCTCAGATT	50717
rs752923101	snp	A/C/T	4.94273e-05	0.00497108	intron-variant	DCAF8	GRCh38.p7	1:160218447	CTTAATCACCTGGAA[A/C/T]CCAAAAAGGTTGGGA	50717
rs752937031	snp	A/G	3.29538e-05	0.00405904	intron-variant	DCAF8	GRCh38.p7	1:160218451	ATCACCTGGAACCCA[A/G]AAAGGTTGGGAAGAG	50717
rs752952784	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160233833	GTAAATGCAGAGTAC[A/C]TTGAACTCTGCAGGG	50717
rs753044737	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160235452	CTTTAAGACAAACAA[A/G]ACAATAAACGATCTA	50717
rs753168982	snp	A/C	8.53905e-05	0.0065336	intron-variant	DCAF8	GRCh38.p7	1:160225171	CCCCCATTTGTTATA[A/C]CATCTTCAGGAAACA	50717
rs753220340	snp	A/G	1.65061e-05	0.00287277	intron-variant	DCAF8	GRCh38.p7	1:160225028	CTAGACAGAGGGGGC[A/G]TGCCAGCCTAGGAGC	50717
rs753223067	snp	A/G	3.29908e-05	0.00406132	intron-variant	DCAF8	GRCh38.p7	1:160244081	TTAGGAAACCACCTG[A/G]GAAAGAAGACAATAG	50717
rs753245584	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160243738	CTTGACCTCTTAGAA[C/G]TACAGCTCTGTTATT	50717
rs753386209	in-del	-/CTCTTCTTCCTC	0.0323896	0.123068	cds-indel, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240083	ACGGCGCCGAGGCTG[-/CTCTTCTTCCTC]CTCTTCTTCCTCCTC	50717
rs753502833	snp	A/T			intron-variant	DCAF8	GRCh38.p7	1:160251048	CCCAGCATTCTCTCA[A/T]ACCAGTGCCTGCCTC	50717
rs753604332	snp	A/C			upstream-variant-2KB	DCAF8	GRCh38.p7	1:160264400	ATAATAAAGTTATAA[A/C]GAGTACTGTAAAGGA	50717
rs753628305	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160253401	GCTGGTAATCCCAGC[A/G]CTTTGGGAGGCTGAG	50717
rs753682351	snp	C/T	1.67332e-05	0.00289246	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160237152	CGCTGGGCGGTCTTG[C/T]CTCAGGTCAATGGTG	50717
rs753743569	snp	C/T	1.64762e-05	0.00287016	intron-variant	DCAF8	GRCh38.p7	1:160218315	AATTCATTTCCAACC[C/T]TAGCTTACCCGGTGA	50717
rs753753498	snp	A/G	1.66571e-05	0.00288587	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160238662	TTCTTGCAACACTGT[A/G]TGGCAGACAGTTCTG	50717
rs753772160	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160222338	AGGGTACGCCCTGAA[C/T]ACTAACGCTTTTTCA	50717
rs753772250	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160238288	GCACCTTGAAACTGT[A/C]AAAATACCCTAAAAA	50717
rs753796531	snp	C/G	6.38957e-05	0.00565188	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160237212	GAACGTACAGGGAGA[C/G]TCTGGTTCCAGTGCC	50717
rs753824352	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160252063	GACTCTAGCAGGTAG[A/C]CTCTAGCTGGGAGTC	50717
rs753996951	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160247042	TCTGCAGAGAACATA[C/T]TTGATTCAAATCCAA	50717
rs754013869	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160262096	GTGCGGCTGGCTCTT[C/G]GGGGCAACACCAGGG	50717
rs754014819	snp	C/T	3.3077e-05	0.00406662	intron-variant	DCAF8	GRCh38.p7	1:160225562	TGAGTCAGGGAAGCC[C/T]GCAGCAACTGGCCCT	50717
rs754038372	snp	C/G	6.63724e-05	0.00576036	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240202	GAGTCCTTATCTTCA[C/G]CTGAGCTCTCTGTGT	50717
rs754148695	in-del	-/TT			intron-variant	DCAF8	GRCh38.p7	1:160228625	TTTTTTTTTTTTTTG[-/TT]GCCACAGGCCAAAAA	50717
rs754186298	snp	G/T			intron-variant	DCAF8	GRCh38.p7	1:160235109	CTTACTCAATACTGG[G/T]ACTGACCTATAAGAT	50717
rs754225028	snp	G/T			utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160216961	AGAGAAGAGAGTGAA[G/T]GATATGTAATCAAGT	50717
rs754313895	snp	A/G	1.74714e-05	0.00295557	intron-variant	DCAF8	GRCh38.p7	1:160225699	AAAATGTAAAAATGT[A/G]CAAACGAAACCCTTG	50717
rs754339828	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160218119	GATAGCATTACACAT[A/G]GACGGCAATGGACAA	50717
rs754384736	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160255511	GATAATGATGAGGAT[C/T]CAAACTATGAATAAG	50717
rs754486094	snp	C/T	1.65067e-05	0.00287282	intron-variant	DCAF8	GRCh38.p7	1:160222632	TAGGGAGCCAGCCAG[C/T]TCAGCACACCATACT	50717
rs754596576	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160251080	TTCTGCTACTCAAGT[A/G]CCCAACTCTCCTACA	50717
rs754623008	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160231014	CCCGCCTCACCTCCC[A/G]AAGTGTCGAGATTAC	50717
rs754648502	snp	G/T			intron-variant	DCAF8	GRCh38.p7	1:160236104	GAGCATTTACATTTT[G/T]TCTGTATACTTTATT	50717
rs754738270	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160237344	TCCAAAAAGAGAAAT[C/G]TCTACCTTTTTGTCA	50717
rs754739478	snp	C/T	9.32097e-05	0.00682614	intron-variant, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239585	AGTAGGGCCATGTCC[C/T]GATATGTAATTCCTA	50717
rs754766623	snp	C/T	1.64732e-05	0.0028699	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160231365	CACATAGATCGTATA[C/T]AGCCCCACTTTCTTC	50717
rs754777334	snp	A/G	1.65102e-05	0.00287312	intron-variant	DCAF8	GRCh38.p7	1:160243917	GAGGAGGACAACCTC[A/G]GTTGATAGTAAAAAT	50717
rs754826104	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160222345	GCCCTGAACACTAAC[A/G]CTTTTTCATTTGGAA	50717
rs754933953	snp	C/T	1.65124e-05	0.00287331	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240293	AACTCAGGTCTGAGG[C/T]CTCCACTTCAATGCC	50717
rs754939549	snp	G/T			intron-variant	DCAF8	GRCh38.p7	1:160223756	TACAAAAATTAGCCA[G/T]GTGTAGAGGCATGCA	50717
rs755003597	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160255677	CAGGCTGGAGTACAC[C/T]GGTGTGATATTGGGT	50717
rs755016273	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160260602	CGAAAACTGCATTTA[C/T]AAGTATGTTCTGACT	50717
rs755017154	snp	A/G	1.64844e-05	0.00287087	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239810	CCAGCCAGGTGCCGC[A/G]CTGGTTAAAGTGCAG	50717
rs755074326	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160217904	TGTAGCGTGAAGGCC[A/G]CCACAGACAATACAC	50717
rs755091604	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160222393	ATAAGTTACATCACT[C/T]AGGACAGGACAGAGG	50717
rs755106390	snp	A/G			intron-variant, nc-transcript-variant	DCAF8	GRCh38.p7	1:160262219	CAGGCCCATCCTTAG[A/G]GGAAACCGGCTGGGA	50717
rs755148634	snp	A/C	3.33178e-05	0.00408139	intron-variant	DCAF8	GRCh38.p7	1:160217757	TGGATGGAACAAGGA[A/C]AAGCCTGTTAGGTCT	50717
rs755198024	snp	A/T			intron-variant	DCAF8	GRCh38.p7	1:160247065	AAATCCAAACTATCT[A/T]CTTCACTTTTCACTG	50717
rs755260115	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160231727	GCTGCAGTCCAACAC[A/G]GTAACAGCCAGTTAT	50717
rs755344363	snp	A/G	1.65545e-05	0.00287697	intron-variant	DCAF8	GRCh38.p7	1:160224575	CAAGAACATAGCAGT[A/G]AAGGCAAAGGCTGAA	50717
rs755349841	snp	C/G			utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160217020	GAATAAGGTGGAAAG[C/G]AAAGTGAAGAGTGTG	50717
rs755358331	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160254035	AAATCTATAAAAATT[A/C]TTTCCTGGGATGGGT	50717
rs755372012	snp	C/T	0.000194496	0.00985952	upstream-variant-2KB	DCAF8	GRCh38.p7	1:160263349	TAAGGTCTGGCCGGG[C/T]GCGGTGGCTCATGCC	50717
rs755373684	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160255732	TCAAGCAATTCTCCC[A/G]CCTCAGCCTCCCAAG	50717
rs755425348	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160235160	TTTTTTTTTGAGACA[C/G]TCTTGCTGTGTCACC	50717
rs755467313	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160240433	CAGGATAGTGACCAC[A/C]TTAGTCTAAGAAATC	50717
rs755532127	snp	C/T	1.64789e-05	0.0028704	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239974	GCTTGCCAGCGAGGT[C/T]GGGGTAGAGCTGATG	50717
rs755539970	snp	C/T	0.000100125	0.00707478	intron-variant	DCAF8	GRCh38.p7	1:160224425	TGGGCCAAAGAAACC[C/T]AGGAAGACAGTCTCA	50717
rs755593199	snp	C/T	4.95193e-05	0.00497566	intron-variant	DCAF8	GRCh38.p7	1:160243923	GACAACCTCAGTTGA[C/T]AGTAAAAATAGCTTC	50717
rs755657992	snp	C/T	7.33608e-05	0.00605599	intron-variant	DCAF8	GRCh38.p7	1:160225712	GTACAAACGAAACCC[C/T]TGAAGAGCTGCAATT	50717
rs755707515	in-del	-/TCA	1.64792e-05	0.00287042	cds-indel, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240022	TCCTCTAGGGCCCGC[-/TCA]TCATCTGATGAGTCC	50717
rs755730841	snp	G/T			intron-variant	DCAF8	GRCh38.p7	1:160261525	ACACACATATGGAAA[G/T]AAAATGAACCAACAT	50717
rs755744240	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160226738	AAAAGAACAATCAAC[A/C]TTCAATATTTCCACT	50717
rs755814231	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160249001	ATTTGAGGCTGGCCT[C/G]ACCAACGTGGTAAAA	50717
rs755879191	snp	C/T	8.23852e-05	0.00641762	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160222661	CTCACCACGCCTCCC[C/T]TGTCCCCCTCCATGA	50717
rs755887892	in-del	-/T			intron-variant	DCAF8	GRCh38.p7	1:160240877	CCTACTTTAAGAAAG[-/T]TATCAGGCCAGGCAC	50717
rs755900426	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160250956	GATCGAAACATCAAC[A/G]TGTAAATATTATTAT	50717
rs756025477	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160236047	CCCTGCCCACAATGG[C/T]TTTCAACAGCTAAAA	50717
rs756081063	snp	G/T			intron-variant	DCAF8	GRCh38.p7	1:160237039	TAGGCACAAAGGTAC[G/T]ATTCGGATGAACCAG	50717
rs756098802	snp	A/C/G	0.000132211	0.00812953	intron-variant	DCAF8	GRCh38.p7	1:160231423	CTTTAAGAGTAGAAA[A/C/G]GCACAGAAAGTTATA	50717
rs756102808	snp	A/C	1.64942e-05	0.00287173	intron-variant	DCAF8	GRCh38.p7	1:160244077	ACAATTAGGAAACCA[A/C]CTGGGAAAGAAGACA	50717
rs756104089	snp	C/T	1.65056e-05	0.00287272	intron-variant	DCAF8	GRCh38.p7	1:160225032	ACAGAGGGGGCATGC[C/T]AGCCTAGGAGCTGGG	50717
rs756111742	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160220580	CTGAGCAGAGAAAAG[A/C]GCTCTGGCCTTAGAT	50717
rs756134693	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160259220	TCATATTATTAAGAC[A/G]GTCCAGCTGTGGAGC	50717
rs756165555	snp	A/C	1.64773e-05	0.00287026	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239999	CTGATGTTTCTGAGG[A/C]CACCCAGTCCTCTAG	50717
rs756246182	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160250185	AAGAGCGAATGCAGG[C/G]CGGCGCAGTGGCTCA	50717
rs756336097	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160251808	CCTCAGGCACTGAAA[C/T]TCAAAGGATGACCCC	50717
rs756383621	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160245740	TAGACAGTTTTGTAT[A/G]GCATTCCTCACACAG	50717
rs756442087	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160230356	GAGCCCAAAGAAACA[C/T]AGTTAAAATAGGCCA	50717
rs756478163	snp	A/G			upstream-variant-2KB	DCAF8	GRCh38.p7	1:160264357	AGTGCAAGGGTTGGG[A/G]GCATAGGAGGAGGGG	50717
rs756512100	snp	C/T	1.70974e-05	0.00292376	missense, nc-transcript-variant, downstream-variant-500B	DCAF8	GRCh38.p7	1:160238729	GAGTAGAATCACCAC[C/T]GTTAGGAAGAAACTT	50717
rs756532174	snp	A/G			downstream-variant-500B	PEA15, DCAF8	GRCh38.p7	1:160215574	CTCCAATTGGAGCCC[A/G]AGCACTGGAAATACG	50717
rs756533833	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160231563	CTGTTTGTTTTGTAC[A/G]TAACAACAGGAAAAA	50717
rs756621717	snp	C/T			utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160216682	TAAGTCCCTTTATTG[C/T]ATTCAGAGAATATAT	50717
rs756690923	snp	A/G	4.96726e-05	0.00498335	intron-variant	DCAF8	GRCh38.p7	1:160225553	CCTTGGGGTTGAGTC[A/G]GGGAAGCCTGCAGCA	50717
rs756732640	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160253871	AGGAGGATAGTCCAT[A/G]CTTCCAAAAAAATAC	50717
rs756737722	in-del	-/TCC	1.70943e-05	0.0029235	cds-indel, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240091	CGAGGCTGCTCTTCT[-/TCC]TCCTCTTCTTCCTCC	50717
rs756750849	snp	C/T	2.01315e-05	0.00317259	intron-variant	DCAF8	GRCh38.p7	1:160237266	CATGAGGTTTCTAAA[C/T]ATTAGAATTAGAGGT	50717
rs756805943	snp	A/G	1.64972e-05	0.00287199	intron-variant	DCAF8	GRCh38.p7	1:160244082	TAGGAAACCACCTGG[A/G]AAAGAAGACAATAGG	50717
rs756820618	snp	A/G			intron-variant, downstream-variant-500B	DCAF8	GRCh38.p7	1:160239203	AGTAAAATCTTTCCA[A/G]AATAACAACAGTATA	50717
rs756822549	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160255306	AAATAGATTTTTTTA[A/C]TATTATTATCGTAGA	50717
rs756871430	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160224125	GGACCACTGACTAAA[A/G]AGGGCTTTCCCTGAC	50717
rs756910442	snp	C/T			missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240184	GTGTCCTCCATGCTG[C/T]CAGAGTCCTTATCTT	50717
rs756929378	snp	C/G	8.23689e-05	0.00641698	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160243977	TTAGCTAAGTCTGTT[C/G]TGCCATCTGTGCTGC	50717
rs756984861	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160247494	TGTTTAAAACTACTG[A/G]GGCTGCTCTTTTCCT	50717
rs757030309	snp	C/T			upstream-variant-2KB	DCAF8	GRCh38.p7	1:160263838	CACTGCCTAGCTCTG[C/T]TCTAGCCTCACTAGC	50717
rs757042799	in-del	-/CT			intron-variant	DCAF8	GRCh38.p7	1:160243836	GTGTAGTTTCCTAAA[-/CT]CAGAACAACACAGGA	50717
rs757088084	snp	A/C	0.000131817	0.00811735	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240002	ATGTTTCTGAGGACA[A/C]CCAGTCCTCTAGGGC	50717
rs757195407	in-del	-/AA			intron-variant, downstream-variant-500B	DCAF8	GRCh38.p7	1:160239065	AGGAAAAATCTACTT[-/AA]TGATTAAGAAAGTAA	50717
rs757199246	snp	C/T	8.35066e-05	0.00646114	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160238676	TGTGGCAGACAGTTC[C/T]GCTACTCGAACCTGC	50717
rs757237442	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160234578	GGCCTAACAGTAGTT[C/T]CCCTCTGAACCTGAT	50717
rs757250554	snp	G/T			intron-variant	DCAF8	GRCh38.p7	1:160235783	TTGCTCCGTCACTCA[G/T]GATGGAGTGCAGTGG	50717
rs757287343	snp	A/G	1.65425e-05	0.00287593	intron-variant	DCAF8	GRCh38.p7	1:160225563	GAGTCAGGGAAGCCT[A/G]CAGCAACTGGCCCTT	50717
rs757347841	in-del	-/AGAA			intron-variant	DCAF8	GRCh38.p7	1:160230110	ATAGGGGAAGAAGAG[-/AGAA]AGAAACAAGGTTTTG	50717
rs757371766	snp	C/G	0.00010545	0.00726043	intron-variant	DCAF8	GRCh38.p7	1:160225700	AAATGTAAAAATGTA[C/G]AAACGAAACCCTTGA	50717
rs757377785	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160219041	ACCACTACTCACCTT[C/G]AGCCAAATAACTGCC	50717
rs757377963	snp	G/T			intron-variant	DCAF8	GRCh38.p7	1:160257958	GGACTTGAACAACTA[G/T]GATCAAGTGATCCTC	50717
rs757523019	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160242532	TATGAGTAACAAATA[C/T]AGACAATTTTGGAGG	50717
rs757523787	snp	C/T	1.67178e-05	0.00289113	intron-variant, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239681	TCTCAGTTGCTATTA[C/T]GCTCCCTTGCCTCAC	50717
rs757546932	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160258921	TTTTCTCCTCCCATC[C/T]TTTCCTTCACCCGAC	50717
rs757548440	snp	C/T			utr-variant-5-prime, nc-transcript-variant, intron-variant	DCAF8	GRCh38.p7	1:160261302	TTCCTCCTTTTATCA[C/T]TGAAGTAAGGCCAGG	50717
rs757612981	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160244235	TAAAATCCATATAAT[C/G]ATATATTTTTGGGGA	50717
rs757654272	snp	A/G	6.60797e-05	0.00574765	intron-variant	DCAF8	GRCh38.p7	1:160218985	TGGTCAGGAAGAAAG[A/G]AAAACACAGACTCAG	50717
rs757657100	snp	C/T	1.81105e-05	0.00300914	intron-variant, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239590	GGCCATGTCCCGATA[C/T]GTAATTCCTACAATA	50717
rs757700516	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160228998	TTGTGTAGGATCAGC[A/G]TGCCTCAAAATCTTC	50717
rs757803774	snp	A/G	2.0672e-05	0.0032149	intron-variant, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239563	TTTAGGTCATTAGGG[A/G]AGCCAAAGTAGGGCC	50717
rs757966617	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160252440	GAGAAAGACATTCCA[A/C]AGGACCAGAGCAAGA	50717
rs757966981	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160235584	GAAAAATCTCCCACA[C/T]TGTAACATGAAATAA	50717
rs758000645	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160237493	TCCTCAAGAGATATG[A/G]ACAGATAGCAAAGAA	50717
rs758008424	snp	A/G			intron-variant, downstream-variant-500B	DCAF8	GRCh38.p7	1:160239054	AAGGAATAGAGGAGG[A/G]AAAATCTACTTTGAT	50717
rs758054598	snp	A/T			intron-variant	DCAF8	GRCh38.p7	1:160253572	AGAATCACTTGAACC[A/T]GGGAGGCAAAGGTTG	50717
rs758096162	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160223839	GGAGGTTGAGGCTGC[A/C]GTGCCTGGGAGGTCA	50717
rs758118744	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160261098	ATAGTTTAGGACAGA[A/C]AGACAAGAAGCCCAC	50717
rs758236805	snp	A/G	3.30011e-05	0.00406195	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160225593	TCATGAATCTTACCA[A/G]GTGATGAGGACAGAA	50717
rs758268479	snp	A/G			synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160225105	GGTGATGTTTGCTTT[A/G]GACTCACTGTTCACC	50717
rs758302043	in-del	-/A			intron-variant	DCAF8	GRCh38.p7	1:160238075	TTCTAAGAGAGTACC[-/A]ACCTCTTTTCATGGC	50717
rs758318987	snp	C/T	3.29516e-05	0.00405891	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160218939	GGTTGCCAGCACAGG[C/T]AGGTGAGGGTGGGGC	50717
rs758399407	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160248632	CCCAGCTACTAGGGA[A/G]GAGGAGGTTGCAGTG	50717
rs758424992	in-del	-/AACA			intron-variant	DCAF8	GRCh38.p7	1:160236274	ACAAACACACACACA[-/AACA]CATACATACACGTAC	50717
rs758457685	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160247234	CTGTTCCTACTCTAA[A/G]AATAACCATAACTCC	50717
rs758536857	snp	A/T			intron-variant	DCAF8	GRCh38.p7	1:160223339	TGAGACTGGCACCCT[A/T]CCTTTATCTGCCTGT	50717
rs758673063	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160256225	GGGAAATCTACTTTT[C/T]ATTTTGTTTCCATCT	50717
rs758715268	in-del	-/A	1.84232e-05	0.003035	intron-variant, downstream-variant-500B	DCAF8	GRCh38.p7	1:160238764	GGGGTGTTAAAAATG[-/A]AAAAAAAGGACACAC	50717
rs758758831	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160252381	GGAAAATTAGCTTTT[A/C]AGATGGGCTTTAAAA	50717
rs758773439	snp	C/G	8.24912e-05	0.00642175	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239802	GCCACTGGCCAGCCA[C/G]GTGCCGCGCTGGTTA	50717
rs758804943	snp	A/G	3.29478e-05	0.00405867	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160222693	CTGAATAATCTGGCA[A/G]GATGATTTCTCCCAG	50717
rs758860781	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160226927	GTAAGTCATATATCC[A/G]TGTGAAAGGTGGTAG	50717
rs758971324	snp	C/G	1.6582e-05	0.00287936	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239730	GTGGCCACTCTCAAA[C/G]TCCAGTACTGGCTGC	50717
rs758992854	in-del	-/A			intron-variant	DCAF8	GRCh38.p7	1:160240873	ATTTCCTACTTTAAG[-/A]AAAGTATCAGGCCAG	50717
rs759016200	snp	C/T			utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160216195	AAGGTTTAAGTCAAA[C/T]CCAGGAAGTCTTTCC	50717
rs759104389	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160246270	TTCACCCCACTATTA[C/T]CCACTCCCAGAGAAT	50717
rs759227992	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160230906	ACACGCATGTACCAC[C/T]ATGCCTGGCTAATTT	50717
rs759243220	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160220636	TGGGATCAAGCATCA[A/G]AGTGCTCTTGGGAGA	50717
rs759249420	in-del	-/A			intron-variant	DCAF8	GRCh38.p7	1:160259981	CTAAGCTGACCAATT[-/A]AAAAATCAGTTGGGA	50717
rs759264455	snp	A/G			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PEA15, DCAF8	GRCh38.p7	1:160215215	GTTCTTTTCAGCAGA[A/G]TCTAGTAGTTTCTCT	50717
rs759290175	snp	A/C	1.64814e-05	0.00287061	intron-variant	DCAF8	GRCh38.p7	1:160244057	TGGGAGAGGAAGAAA[A/C]CAAAACAATTAGGAA	50717
rs759324002	snp	G/T			utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160215986	ATCTGACTGTCCCAG[G/T]ATACAGAATTCTTGG	50717
rs759330947	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160254617	GCCAACATGGTAAAA[C/T]CCCATTTCTACTAAA	50717
rs759368803	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160253415	CACTTTGGGAGGCTG[A/C]GGCGGGTGGATCACC	50717
rs759409017	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160238484	CCACAAATCTTAGGA[A/C]TGAAAGAGGTGAGGC	50717
rs759585222	snp	A/G	1.65061e-05	0.00287277	intron-variant	DCAF8	GRCh38.p7	1:160222803	TGATAAATGAGGGAA[A/G]AAACCACATGAGGGT	50717
rs759590573	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160241175	GAAAGTACCACTACA[C/G]CTTCTGTCACCTAAA	50717
rs759590581	snp	A/T			intron-variant	DCAF8	GRCh38.p7	1:160224839	CTTCAGGACAGGCCC[A/T]GCCAAATATCATCTG	50717
rs759600036	snp	A/C/T	3.29496e-05	0.00405881	synonymous-codon, missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160218435	CCGCTTGTTCTTCTT[A/C/T]ATCACCTGGAACCCA	50717
rs759614609	in-del	-/TA			intron-variant	DCAF8	GRCh38.p7	1:160236291	ATACATACACGTACG[-/TA]TATATATACATACAT	50717
rs759678479	snp	A/T			intron-variant	DCAF8	GRCh38.p7	1:160226372	CAAGACTCCCTCTCC[A/T]TTCCTCATTCTTATC	50717
rs759729001	snp	C/T	8.06809e-05	0.0063509	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160237137	CTGCTACACTTACGA[C/T]GCTGGGCGGTCTTGT	50717
rs759738354	in-del	-/AT			intron-variant	DCAF8	GRCh38.p7	1:160259485	TTGCAGTGGGCTGAG[-/AT]CGCGCCACAGCACCC	50717
rs759802094	snp	C/T	1.70278e-05	0.00291781	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160238607	CAAGGTCTTACTTAC[C/T]TTGTGGGACGCTCCC	50717
rs759840395	snp	C/T	1.70087e-05	0.00291617	intron-variant	DCAF8	GRCh38.p7	1:160225169	CCCCCCCATTTGTTA[C/T]ACCATCTTCAGGAAA	50717
rs759871737	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160248189	GCACATGCCCGTAGT[C/T]CCTGCTACTGGGGAA	50717
rs759900122	snp	A/T	3.34459e-05	0.00408924	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240138	TGAGCGGTCATGGAC[A/T]CGATTTTCATCATTA	50717
rs759945614	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160250322	TACAAAAATATTAGC[C/T]GGGCGTGGTAGTGCA	50717
rs760052420	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160220984	TATGTAAGGAAATTT[A/G]CTTCAGGGGTAGCCT	50717
rs760074779	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160258694	GCTGAGGTGGGAAGA[C/T]CACTTGAGCCCAGGA	50717
rs760114581	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160257509	TCCCCTGATAGAATA[C/T]AAGACTTAGAGCACG	50717
rs760164560	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160243193	CCCAGGTGGTAGTTA[C/T]ACTCTATTAGAATTT	50717
rs760214136	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160245239	TATTTTTTTCAGAGC[C/T]TCACTGCCACCTCCA	50717
rs760387967	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160251073	TGCCTCATTCTGCTA[C/G]TCAAGTGCCCAACTC	50717
rs760409667	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160227963	GCAGTGGTGTAATCA[C/G]AGCTCACTGTAGCCT	50717
rs760414495	snp	A/G	1.66421e-05	0.00288458	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160238657	TTGTATTCTTGCAAC[A/G]CTGTGTGGCAGACAG	50717
rs760425431	snp	A/C	3.30628e-05	0.00406575	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239796	ATCGCTGCCACTGGC[A/C]AGCCAGGTGCCGCGC	50717
rs760486049	in-del	-/G			intron-variant	DCAF8	GRCh38.p7	1:160254055	CTGGGATGGGTGCGT[-/G]GCTCATGCCTGTAAT	50717
rs760499214	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160229651	AAAATTTCAGTGAAT[A/G]CTCAACTTGGAGGAG	50717
rs760695157	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160237942	TACAACTGAAAATCA[A/G]TTAACTAGTGGGTTA	50717
rs760708052	snp	C/T	1.67775e-05	0.00289629	intron-variant	DCAF8	GRCh38.p7	1:160225149	AGATACTGACTGATG[C/T]CCCACCCCCCCATTT	50717
rs760877972	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160223569	TGCAGTCCATCCCTA[C/T]TAAATCAGAATATAT	50717
rs760910324	in-del	-/C	3.37553e-05	0.0041081	intron-variant	DCAF8	GRCh38.p7	1:160225154	CTGACTGATGCCCCA[-/C]CCCCCCATTTGTTAT	50717
rs760917797	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160246937	TCTCTCCAGGCAGGA[C/T]GACAGAGCAAGACAC	50717
rs760927568	snp	A/G	0.000210641	0.0102604	intron-variant, downstream-variant-500B	DCAF8	GRCh38.p7	1:160238789	ACACACAAAAGAAAT[A/G]AGAGAGGTAAACTTG	50717
rs760937270	snp	C/T	1.64776e-05	0.00287028	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160218863	CATCTTTTAACCCTG[C/T]CAGCTCAGTGGAAGC	50717
rs761041984	snp	A/G			utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160215881	CAACATCTGGTCTCA[A/G]AGCTGCTGGGAAAAG	50717
rs761092406	snp	C/T			upstream-variant-2KB	DCAF8	GRCh38.p7	1:160263049	TTCCCAAGAGTGGGC[C/T]GGGTGATGTGGGGTG	50717
rs761179996	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160235183	GTGTCACCCAGGCTG[A/G]AGTACAGTGGCATGA	50717
rs761240699	snp	A/T	1.66682e-05	0.00288684	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240351	TCCAGACATCTCCTC[A/T]GGACTGCTAGACAGG	50717
rs761249246	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160232967	TTCTTCTCAGATCTA[A/G]GCATTCAATTAGTCA	50717
rs761265070	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160217917	CCGCCACAGACAATA[C/T]ACAGAATGGGTATGG	50717
rs761370298	snp	C/T	1.68264e-05	0.0029005	intron-variant	DCAF8	GRCh38.p7	1:160225158	CTGATGCCCCACCCC[C/T]CCATTTGTTATACCA	50717
rs761549031	snp	G/T	1.64749e-05	0.00287005	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160218915	CTTCACATCATGGTC[G/T]AGGCCACTGGTTGCC	50717
rs761559807	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160258526	GGTGCTGCGGCTATG[C/G]CTGTAATCCCAGCAC	50717
rs761584500	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160227490	TCAAACTCCTGGCCT[C/G]AAAAGATTCTCCTGC	50717
rs761591564	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160242013	TTTGGGAGGCCAAGG[C/T]GGGTGGATCACCTAA	50717
rs761671974	snp	C/T	6.25176e-05	0.00559061	intron-variant, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239558	GTGTATTTAGGTCAT[C/T]AGGGGAGCCAAAGTA	50717
rs761681556	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160221950	TGCAGAACTCAAAGG[C/T]CAGGCAGACTATGAT	50717
rs761734413	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160254441	AATTTATATACATAT[A/G]TTTATAAGAAATATT	50717
rs761858602	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160253148	GAGAGCAGAGAGAAA[A/C]ATTGAGAAGAACGAA	50717
rs761912048	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160226368	TCCTCAAGACTCCCT[C/T]TCCTTTCCTCATTCT	50717
rs761944781	snp	A/C/G	3.46736e-05	0.00416363	intron-variant	DCAF8	GRCh38.p7	1:160240397	TGAGGAAGGAGTAGA[A/C/G]GAGAGGGAAAAATAA	50717
rs761950361	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160237886	ACCCTTAAGTGCAGA[A/G]AGAAATGGTGTCCAA	50717
rs761983933	in-del	-/A	1.66286e-05	0.0028834	intron-variant	DCAF8	GRCh38.p7	1:160231445	AAAGTTATATACTCC[-/A]AAAGATCCAAATGGT	50717
rs761989923	snp	C/T	1.65455e-05	0.00287619	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240226	TCTGTGTCTGTGCCT[C/T]GACTTTCTGTGCTGG	50717
rs762065942	snp	A/G	1.65638e-05	0.00287778	intron-variant	DCAF8	GRCh38.p7	1:160222609	CCTACCTTAATGACT[A/G]GAGAGATTAGGGAGC	50717
rs762067539	in-del	-/AAG			intron-variant	DCAF8	GRCh38.p7	1:160261652	AAACAACCTCTCAAC[-/AAG]AAGCCACAGAGCAGG	50717
rs762222837	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160223404	TCTTACCAGCTCAGG[A/G]AAAAAAATAAAACTA	50717
rs762224451	snp	C/T	1.67758e-05	0.00289614	utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160217572	GGCAGCCCCAGCCTG[C/T]CCCACCTAGGTATGA	50717
rs762248679	snp	A/T			intron-variant	DCAF8	GRCh38.p7	1:160245303	AGACCAGAATTTTAT[A/T]AAGCCCTTTCAGTGA	50717
rs762264242	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160247236	GTTCCTACTCTAAAA[A/G]TAACCATAACTCCTG	50717
rs762321825	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160261744	GTAACAATCATGAGT[C/T]AGAAATTCAAGCCAC	50717
rs762407039	snp	C/T	1.67072e-05	0.00289021	intron-variant	DCAF8	GRCh38.p7	1:160231457	TCCAAAAGATCCAAA[C/T]GGTCATGGCAAAGGA	50717
rs762424411	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160231488	GAGCCAAGAGAGTCA[C/T]ATGGCTAATAAGAAA	50717
rs762520132	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160232904	ATCCAGAATAATCTG[C/T]CTAAAACAGCCATAA	50717
rs762593998	snp	C/T	1.64827e-05	0.00287073	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160222773	GGCCATAGAAATTGA[C/T]GCCTTTTACTGAAAT	50717
rs762629924	snp	C/T	1.69539e-05	0.00291147	intron-variant	DCAF8	GRCh38.p7	1:160225679	CTACAGTTGGAAAAG[C/T]AATGAAAATGTAAAA	50717
rs762683522	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160217805	CTTTAGGCCAGAGAT[C/G]AGCAGAATTTTTCTT	50717
rs762710718	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160241514	ACTTTTATCGATCTT[A/G]TCTCCTATAACTACA	50717
rs762717013	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160254915	TGCTTTTGAGTTTTT[A/C]TTTTGTAAAATGGGA	50717
rs762773509	snp	A/G	3.30158e-05	0.00406286	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240074	TGCGCTGTACACGGC[A/G]CCGAGGCTGCTCTTC	50717
rs762800357	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160226456	ATGAGGACACACATA[C/T]TATGTGTCAAATATT	50717
rs762808171	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160256951	ATAAAATTCATCACT[C/T]GCTAATTTTTGAAAA	50717
rs762816059	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160251746	ATGCTTGAGATTACA[A/G]GCACGAGCCACTGCA	50717
rs762843766	snp	C/T			upstream-variant-2KB	DCAF8	GRCh38.p7	1:160263699	AAAACCTCCAATTCC[C/T]ATCACATAATAAAAG	50717
rs762862285	snp	C/T			utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160216516	TTCCCAACCCCTACA[C/T]CAAAGCAGGGAACCA	50717
rs762947432	snp	A/G	1.65395e-05	0.00287567	intron-variant	DCAF8	GRCh38.p7	1:160222622	CTGGAGAGATTAGGG[A/G]GCCAGCCAGCTCAGC	50717
rs762984690	snp	A/C	3.32984e-05	0.00408021	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239753	CTGGCTGCCGCCGTA[A/C]CCAATCCCACACCAC	50717
rs762992498	snp	C/T	3.37115e-05	0.00410543	intron-variant, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239659	TTCTCTAACTCATGC[C/T]TGATTCTCTCAGTTG	50717
rs763081090	snp	C/G	9.31402e-05	0.00682359	intron-variant	DCAF8	GRCh38.p7	1:160237108	CTAAGAGATACAGTT[C/G]TGTAATGATATTACT	50717
rs763096243	snp	A/G	1.64762e-05	0.00287016	utr-variant-5-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160244033	TGTTTGCTGTAGCCA[A/G]CCTGGGTTTGGGAGA	50717
rs763115995	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160251612	CCAGTAGCTGGGACT[A/G]CAGGTGCATACTGCC	50717
rs763132177	snp	A/G	1.64727e-05	0.00286986	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160231356	GGCAGGATTCACATA[A/G]ATCGTATACAGCCCC	50717
rs763248507	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160242407	CAGTTTTTTGAAATG[A/C]AGCTGGGCTTGAGCT	50717
rs763263130	snp	C/T	1.64792e-05	0.00287042	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239924	AGACAAAGCGGGCAC[C/T]TGAACCCAGCTCCCG	50717
rs763298738	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160235461	AAACAAGACAATAAA[C/T]GATCTAGATATCTAT	50717
rs763302115	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160229994	TGTCACTGCACTCCA[C/G]CATGGGTAATAAGAG	50717
rs763350122	snp	A/G			utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160217215	CCCTTGGTACTGAAT[A/G]GCCAGTTGTTCCCCC	50717
rs763384961	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160220067	CTACAGACTTCCCAC[C/T]TACTTTGACTTCCAT	50717
rs763470825	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160259951	AACTCTAGGTGGGCA[A/C]TTACAAAGGACACGT	50717
rs763475475	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160221189	TGCTGGCCTGGGAGA[C/G]GGCATTCAGCCCTGC	50717
rs763536921	snp	C/G	1.64732e-05	0.0028699	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160218419	TATCTTCATCCCGCT[C/G]CCGCTTGTTCTTCTT	50717
rs763596264	snp	C/T	1.69625e-05	0.00291221	intron-variant	DCAF8	GRCh38.p7	1:160224404	GTTCTCCAAAGCCAA[C/T]AGGCTTGGGCCAAAG	50717
rs763597545	snp	C/G	1.65853e-05	0.00287964	intron-variant	DCAF8	GRCh38.p7	1:160217744	TTAGTAACTTCCCTG[C/G]ATGGAACAAGGACAA	50717
rs763651499	snp	C/T			utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160216563	GGATCCTTCCATTCT[C/T]AAGCCTCCTAAAACC	50717
rs763655949	snp	C/T	1.64942e-05	0.00287173	intron-variant	DCAF8	GRCh38.p7	1:160244079	AATTAGGAAACCACC[C/T]GGGAAAGAAGACAAT	50717
rs763690254	in-del	-/A			intron-variant	DCAF8	GRCh38.p7	1:160245033	TTAGGACTAACAGTC[-/A]AGAGTCTCTAAGCAC	50717
rs763692380	snp	C/T	1.65045e-05	0.00287263	intron-variant	DCAF8	GRCh38.p7	1:160224554	GGCCAGGAGCTCTGC[C/T]AAGAACAAGAACATA	50717
rs763743862	snp	A/C	1.648e-05	0.0028705	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239894	GCACAAAGACTCTTG[A/C]CCCACAGGCCTCATA	50717
rs763758199	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160242471	TAACAGGTCTGTAGA[A/G]AAGAAAAAATAAAAC	50717
rs763806415	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160225353	CACTGTCTCATTAGG[C/T]CTCACCATCAAGGTG	50717
rs763816614	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160255057	GACTACATTTCCTAG[A/C]AAATCCTGGACCTCT	50717
rs763862822	snp	A/G	2.10117e-05	0.00324121	intron-variant, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239552	CTTTCAGTGTATTTA[A/G]GTCATTAGGGGAGCC	50717
rs763904700	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160257048	CTTTTCTGACTGATT[C/T]TAACAGCAATGATGT	50717
rs763907889	snp	C/T	1.66454e-05	0.00288486	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160238659	GTATTCTTGCAACAC[C/T]GTGTGGCAGACAGTT	50717
rs763926812	in-del	-/AGAC			intron-variant	DCAF8	GRCh38.p7	1:160225233	CCAGAGATTTGAGAA[-/AGAC]AGACAGAGACAAGAG	50717
rs763961230	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160241521	TCGATCTTATCTCCT[A/G]TAACTACATACTGCA	50717
rs764035401	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160251767	AGCCACTGCACCTGG[C/T]CGTATAGTGTTTATT	50717
rs764059407	snp	C/T			upstream-variant-2KB	DCAF8	GRCh38.p7	1:160263750	GAGGCCATCAAAAAA[C/T]GAATTGCCTCTAAGG	50717
rs764122154	snp	G/T	1.64893e-05	0.0028713	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240065	TAGCCCGCTTGCGCT[G/T]TACACGGCGCCGAGG	50717
rs764235250	snp	A/G	1.64746e-05	0.00287002	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160218882	CTCAGTGGAAGCTTC[A/G]GCTGTGGGTGCCCAG	50717
rs764258265	snp	A/G	6.65646e-05	0.0057687	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240189	CTCCATGCTGTCAGA[A/G]TCCTTATCTTCACCT	50717
rs764360267	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160235630	ATACATATATGTTTA[C/T]ATATACATACAAGTA	50717
rs764420093	snp	A/C			utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160216120	CCCAAGCTCCAGCCA[A/C]TGTAATCAGTCCTTA	50717
rs764448266	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160220069	ACAGACTTCCCACTT[A/G]CTTTGACTTCCATCT	50717
rs764472171	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160258824	AAATACTGATTTACT[A/G]CATATAGATGTCACC	50717
rs764558476	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160244098	AAAGAAGACAATAGG[A/G]ACAAGGAGATTTAAC	50717
rs764686165	in-del	-/AA			intron-variant	DCAF8	GRCh38.p7	1:160221831	CAAAAAAAAAAAAAA[-/AA]AAAAAAAAAGATAAG	50717
rs764700416	snp	C/T			utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160216252	TGGCATGAAGTTGGA[C/T]GGCTTAATGATCAAG	50717
rs764753295	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160231211	GATTCCTATAAAATT[C/T]GTAACTCTCCATAAA	50717
rs764945366	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160238536	CACAATGGGCAGAGA[C/T]AAGGGAGAACCTTGG	50717
rs764996740	snp	A/C	1.65564e-05	0.00287714	intron-variant	DCAF8	GRCh38.p7	1:160222615	TTAATGACTGGAGAG[A/C]TTAGGGAGCCAGCCA	50717
rs765023132	in-del	-/A			intron-variant	DCAF8	GRCh38.p7	1:160218279	CTTTTTAGCCCTCTT[-/A]AAAAGGGTCACTCCC	50717
rs765023956	snp	G/T	8.33855e-05	0.00645645	intron-variant, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239560	GTATTTAGGTCATTA[G/T]GGGAGCCAAAGTAGG	50717
rs765171601	snp	C/T			missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240010	GAGGACACCCAGTCC[C/T]CTAGGGCCCGCTCAT	50717
rs765197073	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160224904	GGTCATCTACTGTAT[A/C]CTCCCGCTATGTGCT	50717
rs765240492	snp	C/G			upstream-variant-2KB	DCAF8	GRCh38.p7	1:160263607	CGCACCACTGCACTC[C/G]AGGCTGGGCAATGGA	50717
rs765296212	in-del	-/G			intron-variant	DCAF8	GRCh38.p7	1:160252828	AGTTCTTAGTCTGGC[-/G]GCCCAGAGAAAATCA	50717
rs765393551	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160259567	AAAACCTCTTCATTC[C/T]TAACTCCCCAGCCCT	50717
rs765396633	snp	A/G	6.59587e-05	0.00574239	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160231347	GTGGGTATTGGCAGG[A/G]TTCACATAGATCGTA	50717
rs765449228	snp	A/C	3.50631e-05	0.00418692	intron-variant	DCAF8	GRCh38.p7	1:160225701	AATGTAAAAATGTAC[A/C]AACGAAACCCTTGAA	50717
rs765505834	snp	C/G	8.27082e-05	0.00643018	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240227	CTGTGTCTGTGCCTC[C/G]ACTTTCTGTGCTGGT	50717
rs765515218	snp	A/G	1.65261e-05	0.0028745	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239798	CGCTGCCACTGGCCA[A/G]CCAGGTGCCGCGCTG	50717
rs765532044	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160248190	CACATGCCCGTAGTC[A/C]CTGCTACTGGGGAAG	50717
rs765546124	snp	C/T	1.65707e-05	0.00287838	intron-variant	DCAF8	GRCh38.p7	1:160217737	AGGCTTGTTAGTAAC[C/T]TCCCTGGATGGAACA	50717
rs765620945	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160233736	AAGTACTGGCTCCAC[A/G]GTTATGTAATCCTGC	50717
rs765621956	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160219933	TTGCAGCTGGACCTA[C/T]AGTCCAAGAAAACAA	50717
rs765648040	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160218274	CTGGAACTTTTTAGC[C/G]CTCTTAAAAGGGTCA	50717
rs765707826	in-del	-/CTGTAATGATATTA	9.30795e-05	0.00682137	intron-variant	DCAF8	GRCh38.p7	1:160237108	CTAAGAGATACAGTT[-/CTGTAATGATATTA]CTGCTACACTTACGA	50717
rs765709447	snp	C/T	1.66991e-05	0.00288951	utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160217583	CCTGCCCCACCTAGG[C/T]ATGAGGCCTCAAGAT	50717
rs765767030	in-del	-/TATA			intron-variant	DCAF8	GRCh38.p7	1:160236321	ATATATACGTGTGTG[-/TATA]TAAATACATATGTGT	50717
rs765841878	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160242181	ACCTGGGAGGTGGAG[A/G]CTGCAGTGAGCCGAG	50717
rs765903782	snp	A/C	1.64825e-05	0.00287071	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160218957	GTGAGGGTGGGGCTC[A/C]AGACAGTTTACCTGG	50717
rs765978244	snp	G/T	1.68499e-05	0.00290253	intron-variant, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239660	TCTCTAACTCATGCC[G/T]GATTCTCTCAGTTGC	50717
rs766091594	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160227986	TGTAGCCTCAAACTC[C/G]TGGGCTCAAGAGATC	50717
rs766169940	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160252062	AGACTCTAGCAGGTA[C/G]ACTCTAGCTGGGAGT	50717
rs766189485	snp	A/G	1.77445e-05	0.00297858	intron-variant	DCAF8	GRCh38.p7	1:160240413	GAGAGGGAAAAATAA[A/G]AAAACAGGATAGTGA	50717
rs766216059	snp	A/G	1.64833e-05	0.00287078	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160222774	GCCATAGAAATTGAC[A/G]CCTTTTACTGAAATG	50717
rs766259418	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160253374	GCGCACAGTGGCTGA[C/G]GTCTAAGTGACGCTG	50717
rs766290147	in-del	-/AT			intron-variant	DCAF8	GRCh38.p7	1:160246630	ACCCTTGTCTCTATA[-/AT]AATCAGTCAAGGAGG	50717
rs766345313	snp	A/T			intron-variant	DCAF8	GRCh38.p7	1:160238247	CAGGTAAGCTGAAGC[A/T]CTCACACAAGAGGAA	50717
rs766353311	in-del	-/AG			intron-variant	DCAF8	GRCh38.p7	1:160252043	AAACAACCCAACTGC[-/AG]AGAGACTCTAGCAGG	50717
rs766356104	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160223571	CAGTCCATCCCTATT[A/C]AATCAGAATATATGG	50717
rs766404969	snp	C/T	3.49125e-05	0.00417792	intron-variant	DCAF8	GRCh38.p7	1:160237114	GATACAGTTCTGTAA[C/T]GATATTACTGCTACA	50717
rs766483026	in-del	-/A			intron-variant	DCAF8	GRCh38.p7	1:160254798	ATCTAAAAAAAAAAG[-/A]AAAAAAGAAAAGTCC	50717
rs766547676	snp	A/G	1.65927e-05	0.00288029	intron-variant	DCAF8	GRCh38.p7	1:160217748	TAACTTCCCTGGATG[A/G]AACAAGGACAAGCCT	50717
rs766567740	snp	A/C/T	8.23627e-05	0.0064168	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160231359	AGGATTCACATAGAT[A/C/T]GTATACAGCCCCACT	50717
rs766602529	snp	C/T	1.65545e-05	0.00287697	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160217614	GGCATGCACTGCACC[C/T]GGTCAGGGCCCTCCT	50717
rs766649195	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160252035	GACAGTACAAACAAC[A/C]CAACTGCAGAGAGAC	50717
rs766671245	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160248168	AAAAATTAGCCGGGC[A/G]TGGTGGCACATGCCC	50717
rs766688438	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160261908	GAATTCTTGGACCTC[A/C]GCCTTCCGTACAAGG	50717
rs766690221	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160246957	GAGCAAGACACAGTC[C/T]CCAAAAAAATAAAAA	50717
rs766728797	in-del	-/AC	1.84783e-05	0.00303954	intron-variant, downstream-variant-500B	DCAF8	GRCh38.p7	1:160238774	AAAATGAAAAAAAGG[-/AC]ACACAAAAGAAATGA	50717
rs766756862	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160233242	ACTTAGTATCTCTGC[A/C]GCTTTTCATTAAATG	50717
rs766766853	snp	C/T	3.29625e-05	0.00405958	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239940	TGAACCCAGCTCCCG[C/T]TCCCGAAGGGCAGGG	50717
rs766813165	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160235073	TATTTTACTTATGTC[C/T]TATGTAAATCATTGC	50717
rs766870112	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160238058	ATATTTTTGCTTAGG[A/G]TTTCTAAGAGAGTAC	50717
rs766922056	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160217987	AGGCCAACTGCCAGT[C/T]TGCCAACCCCTGAAC	50717
rs767069257	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160242801	AAAACTTTACAAAAA[C/G]AAGTGGCAGGCTGGA	50717
rs767112541	snp	A/C	1.65089e-05	0.00287301	intron-variant	DCAF8	GRCh38.p7	1:160222809	ATGAGGGAAGAAACC[A/C]CATGAGGGTTGGCAT	50717
rs767163915	snp	C/T	1.64798e-05	0.00287047	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160222653	ACACCATACTCACCA[C/T]GCCTCCCTTGTCCCC	50717
rs767173530	snp	A/T			intron-variant	DCAF8	GRCh38.p7	1:160245111	TCATCCCATTTCATA[A/T]AATGGCAAACACTGT	50717
rs767301309	in-del	-/A			intron-variant	DCAF8	GRCh38.p7	1:160246630	GACCCTTGTCTCTAT[-/A]AATCAGTCAAGGAGG	50717
rs767323210	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160243127	ATATCCATTTAAAGG[C/T]GGCTTCTCTAATTTA	50717
rs767401990	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160254567	AGGAGGCCGGGCCGG[A/G]TGGATCACGAGGTCA	50717
rs767482560	snp	G/T			intron-variant	DCAF8	GRCh38.p7	1:160222246	GCTTTTATCTGCTAA[G/T]CTAAGATCCAGCCAA	50717
rs767510408	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160236703	ACAAATGAACTGTGA[C/T]AAAACAGAACTCAAC	50717
rs767554809	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160235924	TTGTATTTTTAGTAG[A/G]GGTGAGGTTTTGCCA	50717
rs767571486	snp	C/T	1.6782e-05	0.00289668	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160238619	TACCTTGTGGGACGC[C/T]CCCTTGTGCTGGGCC	50717
rs767598344	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160221956	ACTCAAAGGCCAGGC[A/G]GACTATGATACGATC	50717
rs767681472	snp	A/T			intron-variant	DCAF8	GRCh38.p7	1:160234658	TAAATAAACTTACTA[A/T]CATTTTTTCCTTTTT	50717
rs767742965	snp	A/T			intron-variant	DCAF8	GRCh38.p7	1:160237897	CAGAGAGAAATGGTG[A/T]CCAACTTCATTCCTT	50717
rs767778175	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160261755	GAGTCAGAAATTCAA[C/G]CCACCAGATGCTTTC	50717
rs767837298	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160260052	GAAGCATAAATTAAC[A/G]TATAACTTATTCAAA	50717
rs767842566	snp	A/C	0.000101798	0.00713364	intron-variant	DCAF8	GRCh38.p7	1:160225680	TACAGTTGGAAAAGC[A/C]ATGAAAATGTAAAAA	50717
rs767871140	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160245340	CAAAAGGCACTAGTA[A/G]AAGACAAAGTATAAT	50717
rs767921719	snp	A/G			upstream-variant-2KB	DCAF8	GRCh38.p7	1:160264182	CAACACCTAGAAGAG[A/G]GCTACAGCACAAAGT	50717
rs768015097	snp	A/G	1.64846e-05	0.0028709	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240056	GGTCACGGTTAGCCC[A/G]CTTGCGCTGTACACG	50717
rs768031857	snp	C/T	1.67784e-05	0.00289636	intron-variant	DCAF8	GRCh38.p7	1:160225152	TACTGACTGATGCCC[C/T]ACCCCCCCATTTGTT	50717
rs768055117	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160231492	CAAGAGAGTCACATG[C/G]CTAATAAGAAACCAA	50717
rs768081133	snp	A/G	0.000263644	0.0114783	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240032	CCCGCTCATCATCTG[A/G]TGAGTCCTGGTCACG	50717
rs768145106	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160232906	CCAGAATAATCTGTC[C/T]AAAACAGCCATAATT	50717
rs768234859	snp	A/T			intron-variant	DCAF8	GRCh38.p7	1:160235086	TCCTATGTAAATCAT[A/T]GCCATCCCTTACTCA	50717
rs768282193	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160229043	GGTGGCTCACGACTG[C/T]AATCCCAGCACTTTG	50717
rs768410733	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160220777	ACTTCTAAGATCTTT[A/G]GTTCTAACATTCTAC	50717
rs768484785	snp	A/G	1.66128e-05	0.00288204	intron-variant	DCAF8	GRCh38.p7	1:160218813	ACAGTATGTGGATAA[A/G]CAGAAAGAAAATAAC	50717
rs768528751	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160227423	GCACACACCACCATG[C/T]TGAGCTAATATTTTT	50717
rs768584326	in-del	-/TGTA			intron-variant	DCAF8	GRCh38.p7	1:160236446	ATGTGTGTGTGTGTG[-/TGTA]TATATATATATATAT	50717
rs768676380	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160242937	ACCCAGTGAAAAATA[C/T]GAACCACTTTCCTTT	50717
rs768676460	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160259285	CACACCTGTAATCCT[A/C]GCACTTTGGGAGGCT	50717
rs768693156	snp	A/G	1.64738e-05	0.00286995	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160222711	TGATTTCTCCCAGAG[A/G]AAGATGTGCCCACAG	50717
rs768709547	in-del	-/A			intron-variant	DCAF8	GRCh38.p7	1:160232640	GGGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	50717
rs768748218	snp	G/T	0.000232608	0.0107819	intron-variant	DCAF8	GRCh38.p7	1:160219017	AGTGTGTGGGAGTAG[G/T]GTTTAAAAACCACTA	50717
rs768764254	snp	G/T			intron-variant	DCAF8	GRCh38.p7	1:160244501	TCACAACATAAAGAG[G/T]TGGGTCAGATTCTGA	50717
rs768781557	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160229364	GGAATATTGAGGCTG[A/G]TAAGACACAGAAGAT	50717
rs768798753	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160252884	GTGGGATGAGAAATT[A/G]TTCTGAATAAATTTA	50717
rs768799333	snp	A/C	1.72225e-05	0.00293444	intron-variant, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239616	CAATAACTCACTATC[A/C]GCTCCCAATCCATGC	50717
rs768813831	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160233599	GAGGAGGAGCTGATG[C/T]TGCTCCTTCCCACAG	50717
rs768871849	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160251656	TTTTTTGTAGAGATG[A/G]TGGTGGGGAACATGT	50717
rs768901081	snp	C/T			downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	PEA15, DCAF8	GRCh38.p7	1:160215721	ACACAGAGCAGCAGT[C/T]GGGAGAAGAAAAGCT	50717
rs768924093	in-del	-/ATC			intron-variant	DCAF8	GRCh38.p7	1:160244605	ACTAACTTCAAACCT[-/ATC]ATTATTATTATTCTT	50717
rs768925105	snp	C/G	1.64738e-05	0.00286995	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160231320	CTGATCTCGTCCACC[C/G]ACTGCAAACTGGTGG	50717
rs769043325	snp	G/T	1.66435e-05	0.0028847	intron-variant	DCAF8	GRCh38.p7	1:160231449	TTATATACTCCAAAA[G/T]ATCCAAATGGTCATG	50717
rs769173243	snp	C/T	1.64751e-05	0.00287007	utr-variant-5-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160244021	CATCTTGAATGATGT[C/T]TGCTGTAGCCAGCCT	50717
rs769216451	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160261566	AGCCAGGCAAGTAAT[C/G]TCCCAGCTCCACTAA	50717
rs769259383	snp	A/T	1.65138e-05	0.00287343	intron-variant	DCAF8	GRCh38.p7	1:160231266	ATCAGTCTTACAAAC[A/T]GTCAAAGACACAAAA	50717
rs769306502	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160246274	CCCCACTATTATCCA[C/T]TCCCAGAGAATTCAA	50717
rs769312315	snp	A/T			intron-variant	DCAF8	GRCh38.p7	1:160224243	AAGCAACATTATTGG[A/T]GTGGCAAGAGATGCT	50717
rs769320669	snp	C/G	1.67562e-05	0.00289444	intron-variant	DCAF8	GRCh38.p7	1:160225669	GTCATAAATCCTACA[C/G]TTGGAAAAGCAATGA	50717
rs769320678	snp	C/T	1.65222e-05	0.00287417	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240315	TTCAATGCCTGAGGA[C/T]GTCTCCCTCCCCTCT	50717
rs769381187	in-del	-/T			intron-variant	DCAF8	GRCh38.p7	1:160248883	GTCTACGCAACAGAG[-/T]TGACACCATCTCAAA	50717
rs769394993	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160253424	AGGCTGAGGCGGGTG[A/G]ATCACCTGAGGTCAG	50717
rs769396144	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160247623	AATATTTGCAATATA[C/T]CAGTGGAGCATCTCA	50717
rs769446833	in-del	-/CAGT			intron-variant	DCAF8	GRCh38.p7	1:160245029	TTCCCTTAGGACTAA[-/CAGT]CAGAGTCTCTAAGCA	50717
rs769450532	snp	A/C/G	3.3319e-05	0.0040815	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239752	ACTGGCTGCCGCCGT[A/C/G]CCCAATCCCACACCA	50717
rs769475074	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160234858	GTTCCATTTCCACTA[C/T]AAATCTCCCAGTCTT	50717
rs769490638	in-del	-/CTT			intron-variant	DCAF8	GRCh38.p7	1:160224208	AGTTAGTCTAGCCTC[-/CTT]ATGTCCAAACCAATT	50717
rs769532047	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160232408	AGCACTTTGGGAAGC[C/T]GAGGTGGGTGGATCA	50717
rs769563745	snp	G/T			intron-variant	DCAF8	GRCh38.p7	1:160219215	GTGGCTTCATCCCCA[G/T]ATATGGCCCTAGGGG	50717
rs769567807	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160256717	AATCCACTAGACATA[C/T]TATTAATACATTTCA	50717
rs769577438	in-del	-/A	0.000527974	0.0162391	intron-variant	DCAF8	GRCh38.p7	1:160231274	TACAAACTGTCAAAG[-/A]CACAAAAGAGCCACA	50717
rs769614225	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160236737	AGCTACCAGTATTTT[C/T]GTTCAAATTTTATGT	50717
rs769621984	snp	A/G	3.3018e-05	0.00406299	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160217634	AGGGCCCTCCTCCTC[A/G]TCCGATGTGTCTGAG	50717
rs769655445	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160241430	AAAAGCTGGGCTACT[A/G]TAGTGGTGCCTAAGA	50717
rs769872148	in-del	-/A			upstream-variant-2KB	DCAF8	GRCh38.p7	1:160263476	CTCTACGAAAAATAC[-/A]AAAAAAAAAAAAAAT	50717
rs769900796	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160242759	CATAGACACTACATA[A/C]ACGAACAGGCATGAC	50717
rs769927285	snp	A/G	1.64893e-05	0.0028713	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160224479	CTTGTATCTCTTAAC[A/G]TACTGGGCCCCATCA	50717
rs769966568	snp	A/G			upstream-variant-2KB	DCAF8	GRCh38.p7	1:160263564	GAATTGCTTGAACCC[A/G]GAGGCGGAGGTTGCA	50717
rs769981566	snp	A/G	1.64768e-05	0.00287021	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160222744	ACTACCGCTCACCAC[A/G]AACTCACTCTTGGGG	50717
rs770031522	snp	C/T			upstream-variant-2KB	DCAF8	GRCh38.p7	1:160264501	CCTCTGCTGAGGTGA[C/T]ATCTAAATAAAGGTT	50717
rs770166441	snp	A/G	1.64732e-05	0.0028699	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160218398	ACAGGTCAGTTTGGT[A/G]CAAGCTATCTTCATC	50717
rs770252734	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160246197	AGCAGACCAGTGTAA[C/T]ATGAAGAACAGATCT	50717
rs770339942	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160222982	TAGGGCAGAGGAATC[C/T]GCAGTCCTTTAGCAG	50717
rs770375525	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160244350	GGAACAGGAGGCACA[C/T]ATCAAATGACAGGTA	50717
rs770383678	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160252698	GATAAGAAGTAATGA[C/G]GGGCTGTCTTGGGTT	50717
rs770386145	snp	C/T	1.64963e-05	0.00287192	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160217693	CTGTGGCCCCAACCC[C/T]AGGTTCTCGCCAGCG	50717
rs770429058	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160259520	CCTGGTGACAGAGCA[A/C]GACTCGTCAAAAAAC	50717
rs770439592	snp	C/T	4.97038e-05	0.00498492	intron-variant	DCAF8	GRCh38.p7	1:160231435	AAAAGCACAGAAAGT[C/T]ATATACTCCAAAAGA	50717
rs770439750	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160252771	GTAAAGGTAGATAAT[C/G]TTTAGCTCAATAAGC	50717
rs770452717	in-del	-/AG			utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160216280	AAGCAGCTAAAGGTA[-/AG]AGAGACAGAGTGAGA	50717
rs770469251	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160237683	AGGCACAAGGCACTA[C/T]ACCTGGCTAATTTTT	50717
rs770517215	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160261160	AGAGCTGGAACAAAG[C/T]CAAGAACAACACTCA	50717
rs770635527	snp	C/T	1.64757e-05	0.00287012	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160231310	ACCTTACAAACTGAT[C/T]TCGTCCACCCACTGC	50717
rs770653120	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160246218	GAACAGATCTGATGT[C/T]TTCCCACCTCCATAA	50717
rs770705755	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160232277	ATAATCCCAGCACTT[C/T]GGGAGGAACACTTGA	50717
rs770709214	in-del	-/A			intron-variant	DCAF8	GRCh38.p7	1:160248709	CCATCTCAAAAAAAG[-/A]AAAAAAAAAAAACTG	50717
rs770746802	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160230886	CCTCTTGAGCAGCTG[A/G]GACTACACGCATGTA	50717
rs770874428	snp	C/T	1.64779e-05	0.00287031	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239860	TGGCCCTCAAGCCCA[C/T]GCTGCAGGCGGAAAC	50717
rs770921808	in-del	-/AGAA	8.30792e-05	0.00644459	intron-variant	DCAF8	GRCh38.p7	1:160218815	AGTATGTGGATAAGC[-/AGAA]AGAAAATAACTTCTG	50717
rs770923431	snp	G/T			utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160215909	AAGGGGCAGGAGGAA[G/T]AAGTATCTGGGAATA	50717
rs770965261	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160242083	CCCCCATTTCTACTA[C/G]AAATACAAAAAATTA	50717
rs770987180	snp	C/T	3.29549e-05	0.00405911	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239869	AGCCCATGCTGCAGG[C/T]GGAAACGCTGCACAA	50717
rs771013024	snp	C/G			utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160217235	GTTGTTCCCCCCACC[C/G]CTCCCCCAGCCCAAG	50717
rs771039475	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160243885	CTAAAATCCAGGCCT[C/T]CACTCTATCTTGCAG	50717
rs771099714	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160240992	ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA	50717
rs771106419	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160226279	TCAATGGGTCTGTAA[C/T]CCCTCCTTAAAACTG	50717
rs771241590	snp	A/G	1.65056e-05	0.00287272	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160225069	TCACGTACCTGTGCC[A/G]TCGTGGCTGTACACA	50717
rs771269422	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160224801	TCAAAGGCATAAGAA[C/G]CTGCTCAGGCAAGCA	50717
rs771324305	snp	A/T			intron-variant	DCAF8	GRCh38.p7	1:160220085	CTTTGACTTCCATCT[A/T]ACAAATAAACAAATG	50717
rs771350216	snp	C/G			upstream-variant-2KB	DCAF8	GRCh38.p7	1:160263308	TACAGTTAAACATAA[C/G]GCAGCCAGAGTGCTT	50717
rs771378304	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160251331	ATCAACTAGTTCTAC[C/T]TTCTCCACCTCCAAT	50717
rs771431810	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160249794	GTAGGTCCACACAAT[A/G]GGATACTACTGAGTA	50717
rs771434020	snp	A/C	1.65825e-05	0.00287941	intron-variant	DCAF8	GRCh38.p7	1:160218821	TGGATAAGCAGAAAG[A/C]AAATAACTTCTGCAG	50717
rs771440294	snp	C/T			upstream-variant-2KB	DCAF8	GRCh38.p7	1:160264361	CAAGGGTTGGGAGCA[C/T]AGGAGGAGGGGAGAG	50717
rs771519666	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160235237	CTCCTGGGCTCAAGC[A/G]ATTCTCCTGTCTCAG	50717
rs771567510	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160219586	ATCCTACTACTTGCC[C/G]TGAGCACAACAGGCT	50717
rs771628518	snp	C/T	1.64732e-05	0.0028699	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160218421	TCTTCATCCCGCTCC[C/T]GCTTGTTCTTCTTAA	50717
rs771645268	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160220840	TTGCATGATATAGAA[A/C]TGCTGAGTCTACTAC	50717
rs771676096	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160247480	TACCAAGTGTCTCTT[A/G]TTTAAAACTACTGGG	50717
rs771686897	snp	C/T	1.74903e-05	0.00295717	intron-variant	DCAF8	GRCh38.p7	1:160238575	CACAGAGGATTTGGA[C/T]TGCACAAATTTTGGA	50717
rs771766220	in-del	-/TCCTCTTCCTCT	1.66152e-05	0.00288224	cds-indel, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240106	TCCTCCTCTTCTTCC[-/TCCTCTTCCTCT]TCCTCTGAGCGGTCA	50717
rs771799701	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160259395	AAAATTAGCTGGGCA[C/T]GGTGGCGCATGCCTG	50717
rs771850478	in-del	-/C	1.67384e-05	0.00289291	intron-variant	DCAF8	GRCh38.p7	1:160225149	AGATACTGACTGATG[-/C]CCCACCCCCCCATTT	50717
rs771909314	snp	A/T			upstream-variant-2KB	DCAF8	GRCh38.p7	1:160263381	GTAATCCTAGCACTT[A/T]GGGAGGCGGATGTGG	50717
rs771964960	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160259346	GAGACCACCCTGGCC[A/G]ACATGGTGAAACCCC	50717
rs772014901	snp	C/T	1.67108e-05	0.00289052	intron-variant	DCAF8	GRCh38.p7	1:160225144	GGAGCAGATACTGAC[C/T]GATGCCCCACCCCCC	50717
rs772068022	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160229622	CTGGAGCTCTAAGTA[A/G]GAACTCTCAACTCAA	50717
rs772070140	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160246199	CAGACCAGTGTAACA[C/T]GAAGAACAGATCTGA	50717
rs772088179	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160229429	TCTAAGCCTTACTCT[A/C]ACCCTGGGAAAGTAT	50717
rs772109167	snp	C/G	1.73733e-05	0.00294726	intron-variant, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239609	ATTCCTACAATAACT[C/G]ACTATCAGCTCCCAA	50717
rs772114617	snp	A/G	1.648e-05	0.0028705	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240020	AGTCCTCTAGGGCCC[A/G]CTCATCATCTGATGA	50717
rs772152452	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160253191	AACCTCTGGAAGTCA[A/G]GAATAAAAAGGTTTC	50717
rs772157467	snp	A/G	4.95683e-05	0.00497812	intron-variant	DCAF8	GRCh38.p7	1:160218835	GAAAATAACTTCTGC[A/G]GTCAGCCACTTACAT	50717
rs772202619	snp	A/G	1.64779e-05	0.00287031	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160224504	CCATCACTGTGAGAG[A/G]AGTTGAAGAGGTAAA	50717
rs772216847	snp	A/G	0.000205586	0.0101366	intron-variant, downstream-variant-500B	DCAF8	GRCh38.p7	1:160238781	AAAAAAGGACACACA[A/G]AAGAAATGAGAGAGG	50717
rs772232501	snp	C/T			intron-variant, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239492	ACCCTACCTATGAGG[C/T]TTCCAACAGTCCACA	50717
rs772292419	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160241176	AAAGTACCACTACAC[C/T]TTCTGTCACCTAAAT	50717
rs772435123	in-del	-/TTCT			intron-variant	DCAF8	GRCh38.p7	1:160244616	AACCTATTATTATTA[-/TTCT]TTCTTTTTTTTTTTT	50717
rs772461840	snp	G/T	1.66388e-05	0.00288429	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240346	TCAGCTCCAGACATC[G/T]CCTCTGGACTGCTAG	50717
rs772481841	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160240766	TAAAAAGAAGAGCCA[A/G]CTCCAGCAAGAGCTA	50717
rs772483821	snp	C/T			downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	PEA15, DCAF8	GRCh38.p7	1:160215782	GTGCATGGTTTTTAG[C/T]CCACCCTATCACCCC	50717
rs772497121	snp	C/T			upstream-variant-2KB	DCAF8	GRCh38.p7	1:160264152	AGGACTGTGTTTTTA[C/T]CATCTTTGTAATCTC	50717
rs772502901	in-del	-/C			intron-variant	DCAF8	GRCh38.p7	1:160260878	ACCAAGGGATGACAA[-/C]CCCGAAGCTGTGAGA	50717
rs772511611	snp	C/T	1.65444e-05	0.00287609	intron-variant	DCAF8	GRCh38.p7	1:160218998	AGGAAAACACAGACT[C/T]AGCAGTGTGTGGGAG	50717
rs772719009	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160236376	TGTATATAAACATAT[A/G]TGTGTGTGTATATAT	50717
rs772740255	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160259449	GAGGCAGGAGAATCG[C/G]TTGAACCAGGGAGTC	50717
rs772754319	snp	A/T	1.6513e-05	0.00287336	intron-variant	DCAF8	GRCh38.p7	1:160231268	CAGTCTTACAAACTG[A/T]CAAAGACACAAAAGA	50717
rs772810688	snp	A/T			intron-variant	DCAF8	GRCh38.p7	1:160220962	TCAGCTTACACAGAG[A/T]CAAGAATATGTAAGG	50717
rs772828196	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160244717	CTGCCTCCCGGGTTC[A/G]CACCATTCTCCTGCC	50717
rs772831142	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160258671	GCCCCTGCGGTCCCA[A/G]CTACTCAGCTGAGGT	50717
rs772838006	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160250905	GGTGCCTAGGGTCTA[C/T]GAACACTGGTCTGAC	50717
rs772868623	snp	C/T	1.67172e-05	0.00289108	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240137	CTGAGCGGTCATGGA[C/T]TCGATTTTCATCATT	50717
rs772868762	snp	A/T	0.000135126	0.00821856	intron-variant	DCAF8	GRCh38.p7	1:160225162	TGCCCCACCCCCCCA[A/T]TTGTTATACCATCTT	50717
rs772942213	snp	A/G	4.96471e-05	0.00498208	intron-variant	DCAF8	GRCh38.p7	1:160222621	ACTGGAGAGATTAGG[A/G]AGCCAGCCAGCTCAG	50717
rs772989029	snp	A/G	5.06556e-05	0.00503242	intron-variant, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239655	AGATTTCTCTAACTC[A/G]TGCCTGATTCTCTCA	50717
rs772998859	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160243185	TTAAATAACCCAGGT[C/G]GTAGTTATACTCTAT	50717
rs773003867	snp	C/T			upstream-variant-2KB	DCAF8	GRCh38.p7	1:160263496	AAAAAAAAAATTACC[C/T]GGCATGGTGGAGCGC	50717
rs773084908	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160226528	AGTATCTGTTCTCAC[C/T]CAGTCTCCTCCAATC	50717
rs773174562	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160229650	CAAAATTTCAGTGAA[C/T]GCTCAACTTGGAGGA	50717
rs773210863	snp	G/T			intron-variant	DCAF8	GRCh38.p7	1:160253210	TAAAAAGGTTTCAAG[G/T]TGAGGATAGGCTGGG	50717
rs773252286	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160230657	CGTTTATTTACATAC[A/G]AAAAAGGTAGATTAT	50717
rs773340812	snp	A/G			utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160215883	ACATCTGGTCTCAGA[A/G]CTGCTGGGAAAAGGG	50717
rs773384276	snp	A/G			downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	PEA15, DCAF8	GRCh38.p7	1:160215824	GAACACAGACCACTC[A/G]ATCACCACACATTCC	50717
rs773491214	snp	A/G	1.64784e-05	0.00287035	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160222762	CTCACTCTTGGGGCC[A/G]TAGAAATTGACGCCT	50717
rs773500769	snp	A/G			upstream-variant-2KB	DCAF8	GRCh38.p7	1:160263026	AAGAGAGGTGGTGTG[A/G]GTAAAGGTTCCCAAG	50717
rs773543946	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160224384	AACCTGAGTAAGACA[C/T]TGTGGTTCTCCAAAG	50717
rs773588708	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160247978	CACAAAAAGCACATA[C/T]AAAAAAATTAATCAG	50717
rs773765844	snp	G/T	1.64735e-05	0.00286993	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160218408	TTGGTGCAAGCTATC[G/T]TCATCCCGCTCCCGC	50717
rs773804888	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160243817	ATAGTCCAAGGTGTT[C/T]CCTGTGTAGTTTCCT	50717
rs773872246	snp	A/G	0.000380517	0.0137882	intron-variant	DCAF8	GRCh38.p7	1:160237096	ATATGTTCAAGGCTA[A/G]GAGATACAGTTCTGT	50717
rs773878796	snp	C/T	1.64757e-05	0.00287012	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160231312	CTTACAAACTGATCT[C/T]GTCCACCCACTGCAA	50717
rs773883800	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160235150	AATTTTGGTTTTTTT[C/T]TTTGAGACAGTCTTG	50717
rs773884168	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160217870	TCTATATGGTCTTTA[C/T]TGCAACTATTCAACT	50717
rs773943463	snp	C/T	0.00133244	0.0257769	utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160216909	CCACCTCTTCCCAGC[C/T]TCCCTCACCTGACCT	50717
rs773973683	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160219430	CCCCAGAGAAGAGTC[A/G]GAGAACTATATTCAT	50717
rs774216333	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160229474	GGCAATATGATATAC[A/G]TATCATATGAATACA	50717
rs774222752	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160258496	CCCTGGAAATATAAA[A/C]ATATCTTCAAGCTGG	50717
rs774313299	in-del	-/ACCAT	1.64923e-05	0.00287156	intron-variant	DCAF8	GRCh38.p7	1:160222639	CAGCCAGCTCAGCAC[-/ACCAT]ACCATACTCACCACG	50717
rs774317097	snp	A/T			intron-variant	DCAF8	GRCh38.p7	1:160227441	AGCTAATATTTTTAT[A/T]TTTTGGTGGAGACAG	50717
rs774334380	snp	A/G	1.64789e-05	0.0028704	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160224501	GCCCCATCACTGTGA[A/G]AGGAGTTGAAGAGGT	50717
rs774355322	snp	C/T	1.71193e-05	0.00292564	intron-variant	DCAF8	GRCh38.p7	1:160238603	GGAGCAAGGTCTTAC[C/T]TACCTTGTGGGACGC	50717
rs774473176	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160258822	AGAAATACTGATTTA[C/T]TACATATAGATGTCA	50717
rs774531050	snp	A/G			missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160237201	CCTGCAGATAAGAAC[A/G]TACAGGGAGAGTCTG	50717
rs774658380	snp	A/G	1.64781e-05	0.00287033	intron-variant	DCAF8	GRCh38.p7	1:160244043	AGCCAGCCTGGGTTT[A/G]GGAGAGGAAGAAACC	50717
rs774737129	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160259991	CCAATTAAAAATCAG[C/T]TGGGAAAATTAACCA	50717
rs774760051	snp	C/G/T	4.94542e-05	0.00497243	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240055	TGGTCACGGTTAGCC[C/G/T]GCTTGCGCTGTACAC	50717
rs774892096	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160223367	TGTGTACTGAGATCC[A/C]AGAACAGATTTTTCC	50717
rs774903484	snp	C/T			downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	PEA15, DCAF8	GRCh38.p7	1:160215741	GAAGAAAAGCTTTAC[C/T]GGGAGAAAATACAAC	50717
rs774929886	snp	A/G	1.81089e-05	0.00300901	intron-variant, downstream-variant-500B	DCAF8	GRCh38.p7	1:160238761	GCCTGGGGTGTTAAA[A/G]ATGAAAAAAAGGACA	50717
rs774947300	snp	A/T	1.6569e-05	0.00287824	intron-variant	DCAF8	GRCh38.p7	1:160218826	AAGCAGAAAGAAAAT[A/T]ACTTCTGCAGTCAGC	50717
rs774979882	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160224265	AGAGATGCTCTTGAG[C/T]GCTTTCTCCTCTAGC	50717
rs774997559	snp	C/T			upstream-variant-2KB	DCAF8	GRCh38.p7	1:160262790	CGGATTGGCAGGCCA[C/T]TTCCTGGATGATGGC	50717
rs775000657	snp	C/T	1.64735e-05	0.00286993	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160218423	TTCATCCCGCTCCCG[C/T]TTGTTCTTCTTAATC	50717
rs775001083	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160231480	GCAAAGGAGAGCCAA[A/G]AGAGTCACATGGCTA	50717
rs775001168	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160247632	AATATACCAGTGGAG[C/T]ATCTCAAATCAGAAA	50717
rs775067377	snp	C/T	3.29761e-05	0.00406041	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160217673	AGACTCATCAGAGTC[C/T]GCGTCTGTGGCCCCA	50717
rs775070205	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160257802	CTGCAGTGATCACTG[C/T]GCAATCTCAGCTCTA	50717
rs775095224	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160232851	AAACCCAGCTTAAAA[C/T]ATGCACACTGAAAAC	50717
rs775173329	snp	C/G			utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160216360	AAGTACCACAATAGT[C/G]TGCAGTGGTGGCACC	50717
rs775272496	in-del	-/T			intron-variant	DCAF8	GRCh38.p7	1:160253476	AACATGGTGAAACCC[-/T]GTCTCTACTAAAAAT	50717
rs775363823	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160219339	TTGCCCAAGGCTGGA[A/C]AAAACCATCTCAGTG	50717
rs775404538	snp	A/T			intron-variant	DCAF8	GRCh38.p7	1:160256766	TGTCATATTAATTAC[A/T]CCCCAATGCCCTATT	50717
rs775460223	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160227377	TCACACGATCCTCCC[A/G]CCTCAACCTGCCGCG	50717
rs775490389	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160241501	AAATAACTAGGTCAC[C/T]TTTATCGATCTTATC	50717
rs775530217	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160225148	CAGATACTGACTGAT[A/G]CCCCACCCCCCCATT	50717
rs775537639	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160251709	CTGGACTCAAGTGAT[A/C]CACCTTCCTTGGCCT	50717
rs775573215	snp	C/T	1.64779e-05	0.00287031	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160224508	CACTGTGAGAGGAGT[C/T]GAAGAGGTAAATGTC	50717
rs775603667	in-del	-/C	3.37553e-05	0.0041081	intron-variant	DCAF8	GRCh38.p7	1:160225153	CTGACTGATGCCCCA[-/C]CCCCCCCATTTGTTA	50717
rs775651321	snp	G/T	1.88991e-05	0.00307396	intron-variant, downstream-variant-500B	DCAF8	GRCh38.p7	1:160238784	AAAGGACACACAAAA[G/T]AAATGAGAGAGGTAA	50717
rs775727100	snp	A/T			upstream-variant-2KB	DCAF8	GRCh38.p7	1:160263600	CTGAGATCGCACCAC[A/T]GCACTCCAGGCTGGG	50717
rs775777406	snp	C/T	1.66593e-05	0.00288607	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240350	CTCCAGACATCTCCT[C/T]TGGACTGCTAGACAG	50717
rs775826311	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160221094	TTCCTCACCTGGGCA[A/G]ATGGGTTAATCATCA	50717
rs775929187	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160251576	CTCCCAGGCTCAAGT[C/G]ATGCTCCCACCTCAG	50717
rs775948705	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160251273	GGGTTGATCTCCATC[C/G]AAAGTACAAATTTGC	50717
rs776038139	snp	C/T	1.67069e-05	0.00289019	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240173	AGTAATGACCAGTGT[C/T]CTCCATGCTGTCAGA	50717
rs776070822	snp	A/G	1.65743e-05	0.00287869	intron-variant	DCAF8	GRCh38.p7	1:160219009	GACTCAGCAGTGTGT[A/G]GGAGTAGGGTTTAAA	50717
rs776105019	snp	A/C/G			intron-variant	DCAF8	GRCh38.p7	1:160237701	CTGGCTAATTTTTTC[A/C/G]CTTTTTTTTTGTTTG	50717
rs776164560	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160261188	TCAAGCTCTTTGGGA[A/G]ACTGGTAGGAATTTT	50717
rs776167874	snp	C/T	6.59196e-05	0.00574068	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239917	GCCTCATAGACAAAG[C/T]GGGCACTTGAACCCA	50717
rs776172059	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160244412	AAGCTAACTTCAGCA[C/T]TGCCCCCTAGGCAAG	50717
rs776243337	in-del	-/AG			intron-variant	DCAF8	GRCh38.p7	1:160220184	CCCATTCCACATATC[-/AG]CCTATTGTGAAGTTT	50717
rs776250911	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160244862	GATCCGCCCGCCTCG[C/G]CCTCCCAAAGTGCTG	50717
rs776265328	snp	A/C	1.6857e-05	0.00290314	intron-variant	DCAF8	GRCh38.p7	1:160225155	TGACTGATGCCCCAC[A/C]CCCCCATTTGTTATA	50717
rs776296304	snp	C/T			utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160216044	AAATAGCAGCAAAAG[C/T]ACTTAAGGGCAAGAA	50717
rs776340797	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160229839	CTAGCCTGGCTAACA[C/T]GGTGAGACCTCGGTT	50717
rs776375262	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160253111	GAATCTTGAGGAATA[A/C]CTACCCTTAGAGAAG	50717
rs776475469	snp	C/T	2.0867e-05	0.00323003	intron-variant, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239557	AGTGTATTTAGGTCA[C/T]TAGGGGAGCCAAAGT	50717
rs776596898	snp	A/T			utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160215963	CCTTCCTGGCCTGAT[A/T]TAGAAGAATCTGACT	50717
rs776614834	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160254576	GGCCGGGTGGATCAC[A/G]AGGTCAAGAGATCAA	50717
rs776623943	snp	C/G			synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239919	CTCATAGACAAAGCG[C/G]GCACTTGAACCCAGC	50717
rs776684358	snp	A/T			utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160217376	CGAGTCCTATGCACC[A/T]CTCCATAGAGCCCCA	50717
rs776713807	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160224613	GGGACCAGGAGGTGG[A/G]GGTTGGGGTGGGGCT	50717
rs776744486	snp	A/G	4.94222e-05	0.00497078	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160222717	CTCCCAGAGGAAGAT[A/G]TGCCCACAGTCACTA	50717
rs776784314	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160244229	TATGTTTAAAATCCA[C/T]ATAATGATATATTTT	50717
rs776795592	snp	G/T	1.65666e-05	0.00287802	intron-variant	DCAF8	GRCh38.p7	1:160222601	TGCTAAAACCTACCT[G/T]AATGACTGGAGAGAT	50717
rs776849512	snp	C/T	3.38249e-05	0.00411234	intron-variant, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239652	TTCAGATTTCTCTAA[C/T]TCATGCCTGATTCTC	50717
rs776905354	in-del	-/AG	1.65466e-05	0.00287628	intron-variant	DCAF8	GRCh38.p7	1:160231428	AGAGTAGAAAAGCAC[-/AG]AAAGTTATATACTCC	50717
rs777165555	snp	A/G	1.64727e-05	0.00286986	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160231336	ACTGCAAACTGGTGG[A/G]TATTGGCAGGATTCA	50717
rs777167629	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160250243	CCAAGGCGGGCAGAT[A/C]ACCTGAGGTCAGGAG	50717
rs777246803	snp	A/C	1.64757e-05	0.00287012	utr-variant-5-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160244030	TGATGTTTGCTGTAG[A/C]CAGCCTGGGTTTGGG	50717
rs777267214	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160242155	GAGGCTGAGGCAGAA[A/G]AATCGCTTGAACCTG	50717
rs777299798	snp	A/G	3.44768e-05	0.00415177	intron-variant	DCAF8	GRCh38.p7	1:160240392	GTTAGTGAGGAAGGA[A/G]TAGAGGAGAGGGAAA	50717
rs777317280	snp	A/G	3.30066e-05	0.00406229	intron-variant	DCAF8	GRCh38.p7	1:160243925	CAACCTCAGTTGATA[A/G]TAAAAATAGCTTCAC	50717
rs777341297	in-del	-/A/AA			upstream-variant-2KB	DCAF8	GRCh38.p7	1:160263475	CTCTACGAAAAATAC[-/A/AA]AAAAAAAAAAAAAAA	50717
rs777366581	snp	C/G	1.65302e-05	0.00287486	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240320	TGCCTGAGGATGTCT[C/G]CCTCCCCTCTTCAGC	50717
rs777407151	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160235632	ACATATATGTTTATA[C/T]ATACATACAAGTATA	50717
rs777446410	snp	G/T			utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	DCAF8	GRCh38.p7	1:160262517	GCTGCCACGCTTTCC[G/T]GCCCCGTTTGCGACG	50717
rs777538094	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160247380	ATAAAGCCTTAAATT[C/T]TTAACCAATTACATG	50717
rs777544982	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160224049	CTTCTGCCTCATCTA[A/G]AAGAATTGTTTACTC	50717
rs777550489	in-del	-/C			intron-variant	DCAF8	GRCh38.p7	1:160231918	CTTATGGCCAGGTAT[-/C]GGTGGCTCATGCCTG	50717
rs777569534	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160261113	AAGACAAGAAGCCCA[C/G]AGACAATTAAACTTG	50717
rs777574276	snp	C/T	1.64784e-05	0.00287035	intron-variant	DCAF8	GRCh38.p7	1:160218309	CTTGGGAATTCATTT[C/T]CAACCCTAGCTTACC	50717
rs777619109	snp	A/T			intron-variant	DCAF8	GRCh38.p7	1:160229556	CATTCCCCTCCAAAC[A/T]TCTTGGTCCTAGTGG	50717
rs777631572	snp	C/T	6.26311e-05	0.00559568	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160237200	ACCTGCAGATAAGAA[C/T]GTACAGGGAGAGTCT	50717
rs777706494	snp	G/T	1.64882e-05	0.00287121	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160217674	GACTCATCAGAGTCC[G/T]CGTCTGTGGCCCCAA	50717
rs777805700	snp	A/G	3.29641e-05	0.00405968	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160224491	AACATACTGGGCCCC[A/G]TCACTGTGAGAGGAG	50717
rs777857193	in-del	-/TAAA			intron-variant	DCAF8	GRCh38.p7	1:160252954	TTTAAGTTTGGAACT[-/TAAA]TAAATAAAGTAAGGC	50717
rs777867137	snp	A/G	1.64776e-05	0.00287028	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239847	GACACAACCAGTATG[A/G]CCCTCAAGCCCATGC	50717
rs777946520	snp	A/G	1.65053e-05	0.0028727	intron-variant	DCAF8	GRCh38.p7	1:160225033	CAGAGGGGGCATGCC[A/G]GCCTAGGAGCTGGGC	50717
rs778005634	snp	C/T	3.29544e-05	0.00405908	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240000	TGATGTTTCTGAGGA[C/T]ACCCAGTCCTCTAGG	50717
rs778029233	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160240779	CAACTCCAGCAAGAG[C/T]TAGCATAGCCATCTT	50717
rs778139720	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160242174	CGCTTGAACCTGGGA[A/G]GTGGAGGCTGCAGTG	50717
rs778221298	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160223726	AACATGGTGAAACCC[A/C]ATCTCCACAAAAAAT	50717
rs778274142	snp	A/G	1.65996e-05	0.00288089	intron-variant	DCAF8	GRCh38.p7	1:160218816	GTATGTGGATAAGCA[A/G]AAAGAAAATAACTTC	50717
rs778276680	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160256400	AAAACCTCAAGAAGT[A/G]CCTTCCTACAGGTTA	50717
rs778282117	snp	A/C/G	9.23957e-05	0.00679635	intron-variant, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239586	GTAGGGCCATGTCCC[A/C/G]ATATGTAATTCCTAC	50717
rs778335413	snp	A/G	1.78007e-05	0.00298329	intron-variant, downstream-variant-500B	DCAF8	GRCh38.p7	1:160238751	AAGAAACTTGGCCTG[A/G]GGTGTTAAAAATGAA	50717
rs778336122	snp	A/G	1.75449e-05	0.00296178	intron-variant	DCAF8	GRCh38.p7	1:160238563	TTGGCTGAGAACCAC[A/G]GAGGATTTGGATTGC	50717
rs778391071	snp	C/T	1.64743e-05	0.00287	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160218334	CTTACCCGGTGATGG[C/T]GTCTCTGTCTCAGGT	50717
rs778578196	snp	C/T	4.97211e-05	0.00498579	intron-variant	DCAF8	GRCh38.p7	1:160231437	AAGCACAGAAAGTTA[C/T]ATACTCCAAAAGATC	50717
rs778603719	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160220792	GGTTCTAACATTCTA[C/T]GTTACAATTACATTC	50717
rs778633124	snp	C/T	1.64741e-05	0.00286998	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160243980	GCTAAGTCTGTTCTG[C/T]CATCTGTGCTGCTCC	50717
rs778642785	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160245951	CGAGACCAGCCTGAG[C/T]AACATGGAGAAACCC	50717
rs778696420	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160237410	TACTCTTGTTCTATG[C/T]GAATTATTTATAGTT	50717
rs778731754	snp	A/G					GRCh38.p7	1:160231324	TCTCGTCCACCCACT[A/G]CAAACTGGTGGGTAT	50717
rs778736929	in-del	-/TCCTCCTCTTCC	1.65935e-05	0.00288036			GRCh38.p7	1:160240102	TCTTCCTCCTCTTCT[-/TCCTCCTCTTCC]TCCTCCTCTTCCTCT	50717
rs778766997	snp	A/G	1.64827e-05	0.00287073	intron-variant	DCAF8	GRCh38.p7	1:160218469	AGGTTGGGAAGAGGG[A/G]GCAGCAATGAAGAGG	50717
rs778846319	snp	A/C	1.65108e-05	0.00287317	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160225084	GTCGTGGCTGTACAC[A/C]AGACAGGTGATGTTT	50717
rs778901753	snp	C/G	3.29587e-05	0.00405934	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240015	CACCCAGTCCTCTAG[C/G]GCCCGCTCATCATCT	50717
rs778930916	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160218448	TTAATCACCTGGAAC[A/C]CAAAAAGGTTGGGAA	50717
rs778955754	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160231847	GAATCCCAGAAACAG[C/T]AGGCTAAAAAAGACC	50717
rs778963011	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160244531	AGTATCATTTTACAC[A/G]CAAATCAACAGAAAT	50717
rs778966689	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160260776	GTCGGAATTCTGAAA[C/T]AGACTGGACTCAGAC	50717
rs779045417	snp	A/G			utr-variant-3-prime, nc-transcript-variant	DCAF8	GRCh38.p7	1:160217055	GGTTAGGGGCTTTAA[A/G]GACTTCCCAGGAAAA	50717
rs779054504	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160230536	TATGGATAAAAAAAA[C/G]TGGTAGCTCAGGACA	50717
rs779180890	snp	A/G			intron-variant, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239350	GAAGACAAAGGTAAA[A/G]TAACTTGGCCAAGAT	50717
rs779183169	snp	A/G	3.30409e-05	0.0040644	intron-variant	DCAF8	GRCh38.p7	1:160218986	GGTCAGGAAGAAAGG[A/G]AAACACAGACTCAGC	50717
rs779210703	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160222835	GGCATCAGGCCTATA[C/T]ACATTCATCTCAAAG	50717
rs779218449	snp	A/G	1.65272e-05	0.0028746	intron-variant	DCAF8	GRCh38.p7	1:160225569	GGGAAGCCTGCAGCA[A/G]CTGGCCCTTCATGAA	50717
rs779242109	snp	C/T	8.91035e-05	0.00667412	intron-variant, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239596	GTCCCGATATGTAAT[C/T]CCTACAATAACTCAC	50717
rs779270753	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160252353	GTTTCAGGGAAAAAC[A/G]AAATGCTTCCATGGA	50717
rs779376145	snp	C/T	5.00313e-05	0.00500131	intron-variant, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239686	GTTGCTATTATGCTC[C/T]CTTGCCTCACCTGGA	50717
rs779452991	snp	A/T			intron-variant	DCAF8	GRCh38.p7	1:160240685	AGTGTGCCTGATACA[A/T]CTACCATTGGCTCTG	50717
rs779539012	in-del	-/TAT			intron-variant	DCAF8	GRCh38.p7	1:160228733	TGAGGATCAGTAAGC[-/TAT]TATTTCTCTATATTC	50717
rs779632181	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160225897	CACCCAGGCTGTAGT[A/G]CAGTGGCATGACCCC	50717
rs779709016	snp	C/G	1.6473e-05	0.00286988	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160218386	TGTGACTATCAAACA[C/G]GTCAGTTTGGTGCAA	50717
rs779740369	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160250993	TGATCCCTTTACTAA[A/G]ACCTGAATTCGGTCT	50717
rs779742527	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160234968	GAAATTCTTCTACTA[C/T]CCAAACAGCTTTTTC	50717
rs779760250	snp	A/G	1.65252e-05	0.00287443	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240246	TTCTGTGCTGGTGCG[A/G]TTGGGGCCACCATCA	50717
rs779760977	snp	G/T			intron-variant	DCAF8	GRCh38.p7	1:160240921	TGTAATCCCAGCACT[G/T]TGGGAGGCCGAGGCA	50717
rs779800545	snp	A/G	5.04104e-05	0.00502023	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160238697	TCGAACCTGCCCGTC[A/G]CGGGCACACATGGCC	50717
rs779804738	in-del	-/AT/CAAA			intron-variant	DCAF8	GRCh38.p7	1:160236276	AAACACACACACACA[-/AT/CAAA]TACATACACGTACGT	50717
rs779809514	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160220676	TGTCCTCTGATACCA[C/T]CCCCAACCCTTGTCC	50717
rs779837597	in-del	-/GTCAGA	0.000116637	0.00763575	cds-indel, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240183	AGTGTCCTCCATGCT[-/GTCAGA]GTCCTTATCTTCACC	50717
rs779872030	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160261547	AACCAACATGAAGAT[C/T]AGAAGCCAGGCAAGT	50717
rs779999241	snp	G/T	1.66507e-05	0.00288532	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240111	CTCTTCTTCCTCCTC[G/T]TCCTCTTCCTCTGAG	50717
rs780045484	snp	G/T	1.6495e-05	0.0028718	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160225615	AGGACAGAACTTCTT[G/T]AGTACTCCATTGTTC	50717
rs780135855	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160258104	GTAATCCCAGCACTC[C/T]GGGAGGCTGAGGCAG	50717
rs780165292	snp	A/G	6.91336e-05	0.00587895	intron-variant, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239613	CTACAATAACTCACT[A/G]TCAGCTCCCAATCCA	50717
rs780225645	snp	G/T			intron-variant	DCAF8	GRCh38.p7	1:160259253	AAAAAAGAACTCTTT[G/T]GCCGGGCATGGTGGT	50717
rs780276373	in-del	-/G			intron-variant, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239523	TGCTCAAGGAATCTA[-/G]GGTTGCCAAGAGTCT	50717
rs780304484	snp	G/T			intron-variant	DCAF8	GRCh38.p7	1:160229107	TTCGAGACCAGCCTG[G/T]CCAACATGGCAAAAC	50717
rs780377544	snp	A/G	3.29473e-05	0.00405864	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160222697	ATAATCTGGCAGGAT[A/G]ATTTCTCCCAGAGGA	50717
rs780420589	in-del	-/AG			intron-variant	DCAF8	GRCh38.p7	1:160258947	CCGACATGGATCTTC[-/AG]AGTTCATAAAAACAC	50717
rs780578446	snp	C/G			intron-variant	DCAF8	GRCh38.p7	1:160253917	GTCAAAAGGCTGTAA[C/G]AGTCAGAACAGCTTT	50717
rs780633765	in-del	-/TATTACT	0.000192771	0.00981572	upstream-variant-2KB	DCAF8	GRCh38.p7	1:160263233	TTCCAAGTCATTACA[-/TATTACT]TAAGACTACCGCAAT	50717
rs780659649	in-del	-/CCA			intron-variant	DCAF8	GRCh38.p7	1:160242701	AGACCATACGGAGCT[-/CCA]CCACAACTACTCAAC	50717
rs780681717	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160246847	TGTAGTCCCAGCTAC[C/T]TGGGGTAGGGCTGAG	50717
rs780727897	in-del	-/ACACAT/ACAT			intron-variant	DCAF8	GRCh38.p7	1:160236279	CACACACACACATAC[-/ACACAT/ACAT]ATACACGTACGTATA	50717
rs780736325	snp	A/G	0.00015041	0.00867077	missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240128	CCTCTTCCTCTGAGC[A/G]GTCATGGACTCGATT	50717
rs780761724	snp	C/T			intron-variant, downstream-variant-500B	DCAF8	GRCh38.p7	1:160239215	CCAGAATAACAACAG[C/T]ATAAGCTAACATTTA	50717
rs780857370	snp	A/G			missense, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240214	TCACCTGAGCTCTCT[A/G]TGTCTGTGCCTCGAC	50717
rs780878725	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160248874	CTGCACTCCAGTCTA[C/T]GCAACAGAGTGACAC	50717
rs780884914	snp	C/T	1.65015e-05	0.00287237	intron-variant	DCAF8	GRCh38.p7	1:160231417	AGTTTCCTTTAAGAG[C/T]AGAAAAGCACAGAAA	50717
rs780931358	snp	A/G	3.30191e-05	0.00406306	intron-variant	DCAF8	GRCh38.p7	1:160218980	TTACCTGGTCAGGAA[A/G]AAAGGAAAACACAGA	50717
rs780947541	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160225489	CAAATCCAGATGACT[A/G]ACTTGAAAGTCCAAG	50717
rs780983185	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160247538	AGATCTGCATAAGAG[A/C]CTACGTATCCCTTGT	50717
rs781055980	in-del	-/AAAAAAAAAAAA			intron-variant	DCAF8	GRCh38.p7	1:160253655	CTCCATCTCAAAAAA[-/AAAAAAAAAAAA]AAAAAAAAAAAATAG	50717
rs781068960	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160232301	CACTTGAGGCTAGGA[A/G]CTCAAGATCACCCTG	50717
rs781108558	snp	C/G	1.65105e-05	0.00287315	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160240297	CAGGTCTGAGGCCTC[C/G]ACTTCAATGCCTGAG	50717
rs781238757	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160259110	GACACAGCTGCTTTC[A/G]TTGTGATATTATCAG	50717
rs781248232	snp	C/T	1.6537e-05	0.00287545	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160224443	GAAGACAGTCTCACC[C/T]GTGGCATTATTTCTG	50717
rs781341973	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160219106	AGGCCCACCCATCCT[A/G]AGCCTAAGCCAAAGG	50717
rs781350797	snp	A/T			intron-variant	DCAF8	GRCh38.p7	1:160258037	CACTCAGCCTGGCAG[A/T]TTCTTATACATTTAA	50717
rs781377478	snp	A/G	1.64787e-05	0.00287038	synonymous-codon, nc-transcript-variant	DCAF8	GRCh38.p7	1:160239825	GCTGGTTAAAGTGCA[A/G]GGTATTGACACAACC	50717
rs781438350	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160220237	GTGCAGTTAAAGTCC[A/C]ATGCCTGGAATAGTA	50717
rs781449505	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160227232	AACACTGAGGAGTGG[C/T]TGGACATCAAGGAGA	50717
rs781537295	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160229020	AAAATCTTCACATAG[A/C]CAGGCGCGGTGGCTC	50717
rs781585009	snp	C/T			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PEA15, DCAF8	GRCh38.p7	1:160215328	TGTCTGCAGTGTGCA[C/T]GGCCTTGTTCTAACC	50717
rs781602578	snp	A/G			intron-variant	DCAF8	GRCh38.p7	1:160224950	CTCCCCAGCTGCTCT[A/G]CTTGGAGCTATAGCA	50717
rs781665932	snp	A/G			utr-variant-5-prime, nc-transcript-variant, intron-variant	DCAF8	GRCh38.p7	1:160261320	AAGTAAGGCCAGGCT[A/G]AGCTCCTGAGAAAAT	50717
rs781727528	snp	G/T	0.000735564	0.0191635	upstream-variant-2KB	DCAF8	GRCh38.p7	1:160263384	ATCCTAGCACTTTGG[G/T]AGGCGGATGTGGGCG	50717
rs781762894	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160251422	CTTCACAAGAAACAC[C/T]TACTTCTCCAAGCCT	50717
rs796112333	in-del	-/A			intron-variant	DCAF8	GRCh38.p7	1:160219764	TCCGAAAGGCACCCA[-/A]TGCCCCCTGCTGTCT	50717
rs796118745	multinucleotide-polymorphism	CA/TG			intron-variant	DCAF8	GRCh38.p7	1:160235226	CAACCTCCACCTCCT[CA/TG]GCTCAAGCGATTCTC	50717
rs796189653	in-del	-/A			intron-variant	DCAF8	GRCh38.p7	1:160234817	AAAGCTAGTACTAGA[-/A]GGCAGAACCCTTGTC	50717
rs796190727	in-del	-/A			intron-variant	DCAF8	GRCh38.p7	1:160258599	AGACCTCATCTCTTT[-/A]AAAAAAACAAACAAA	50717
rs796290674	in-del	-/A			intron-variant	DCAF8	GRCh38.p7	1:160258615	AAAAAACAAACAAAC[-/A]AAAAAAAAAACAACC	50717
rs796296873	in-del	-/A			intron-variant	DCAF8	GRCh38.p7	1:160256578	GAAAAAGCCAGGAAG[-/A]AAAAAAAAAATGGCA	50717
rs796325294	snp	A/C			intron-variant	DCAF8	GRCh38.p7	1:160250559	CATTAAAAACACTAA[A/C]TTCTCAAGGCTGTGA	50717
rs796428615	in-del	-/A			intron-variant	DCAF8	GRCh38.p7	1:160248895	GAGTGACACCATCTC[-/A]AAAAAAAAAAAAGAG	50717
rs796487656	snp	C/T			intron-variant	DCAF8	GRCh38.p7	1:160235247	CAAGCGATTCTCCTG[C/T]CTCAGCCTCCTGAGT	50717
rs796491255	in-del	-/AA			intron-variant	DCAF8	GRCh38.p7	1:160236262	TGAGGCATCACACAC[-/AA]ACACACACACACATA	50717
rs796503166	in-del	-/CC			intron-variant	DCAF8	GRCh38.p7	1:160227875	GAACATATGATAGGC[-/CC]TTGATAGTTTATATT	50717
rs796503680	in-del	-/AA			intron-variant	DCAF8	GRCh38.p7	1:160234243	GTGAGACTGCACCTC[-/AA]AAAAAAAAAAAAATG	50717
rs796728326	in-del	-/ACAT			intron-variant	DCAF8	GRCh38.p7	1:160236274	CACAAACACACACAC[-/ACAT]ACATACACGTACGTA	50717
rs796799398	in-del	-/A			intron-variant	DCAF8	GRCh38.p7	1:160256577	GAAAAAGCCAGGAAG[-/A]AAAAAAAAAAATGGC	50717
rs796827119	in-del	-/GTTTTT			intron-variant	DCAF8	GRCh38.p7	1:160233060	AGAGGCTTGGCTTTA[-/GTTTTT]GTTTTTAAGTCTAAG	50717
rs796979805	in-del	-/AT			intron-variant	DCAF8	GRCh38.p7	1:160236276	CAAACACACACACAC[-/AT]ACATACACGTACGTA	50717

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