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

HDAC6

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs1467379	snp	C/T	0	0				:	GCACAGGCTTCACCG[C/T]CAACGTGGCATGGAA	10013
rs4411026	snp	A/C	0	0				:	TCCCTTACTCCCTTT[A/C]TGGCTCCCCACTGTC	10013
rs34826345	snp	A/C	0.375	0.216506				:	TGGTACATTTGTATC[A/C]CCAACTCTTGGCACA	10013
rs35189789	snp	A/G	0	0				:	ATCTTAGGCTTTGCA[A/G]GCCACATACGGTCTC	10013
rs1127346	snp	C/T	0	0	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823380	CACTGGCCCAGACCA[C/T]CTCGGAGGCAGCCAT	10013
rs1985411	snp	A/C	0.447863	0.152807	intron-variant	HDAC6	GRCh38.p7	X:48819689	agacgtggtggcggg[A/C]gcctgtagtcccagc	10013
rs2008290	snp	C/G	0.119068	0.212972	intron-variant	HDAC6	GRCh38.p7	X:48810110	agacagggtatcact[C/G]tgtcacccaggctgg	10013
rs2075837	snp	A/G	0.35347	0.227583	intron-variant	HDAC6	GRCh38.p7	X:48818432	AGCTCAGGATAGATC[A/G]CAGGACGTATGTGAC	10013
rs2075840	snp	A/G	0.369713	0.219474	intron-variant	HDAC6	GRCh38.p7	X:48814381	GCAACTGTTGGGTTG[A/G]GGGTGTCTATGGGGA	10013
rs5905711	snp	A/C/G	0.001583	0.0280909	intron-variant	HDAC6	GRCh38.p7	X:48816100	TGGGGGTCCCTCCCC[A/C/G]TCAGGCACTAAGCCT	10013
rs5906711	snp	C/T	0.446659	0.154354	intron-variant	HDAC6	GRCh38.p7	X:48809768	GATCGCACCACTGCA[C/T]TCCAGCCTGGGTGAT	10013
rs5906712	snp	C/G	0.420951	0.182417	intron-variant	HDAC6	GRCh38.p7	X:48817519	ACCTGGATGCTCCCC[C/G]CAGCCCATTGTTTAC	10013
rs5906713	snp	C/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48817852	GAAGAGCCCAGGGCC[C/T]AGCCCCGAGCACTTG	10013
rs6609797	snp	C/T	0.00211696	0.0324653	intron-variant	HDAC6	GRCh38.p7	X:48821498	acctgCCTCtttttt[C/T]ttttttttttttttt	10013
rs12397055	snp	G/T			intron-variant	HDAC6	GRCh38.p7	X:48810727	aatcctcatgcctca[G/T]cctcctgagtagctg	10013
rs12557774	snp	C/G			intron-variant, utr-variant-3-prime	HDAC6	GRCh38.p7	X:48806867	TTGTCACCCAGACAC[C/G]TGCCTCCTCTCATGG	10013
rs12847613	snp	G/T	0	0	intron-variant	HDAC6	GRCh38.p7	X:48813237	TTTTATGTCCTACTG[G/T]GTTTCTCTTCCTCTA	10013
rs17281209	snp	A/G	0.0389457	0.134	upstream-variant-2KB	HDAC6	GRCh38.p7	X:48800821	AGCTGACATTTAGAC[A/G]TGGAGTGGGAGTTGC	10013
rs17281216	snp	C/T	0.0256233	0.11025	intron-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	HDAC6	GRCh38.p7	X:48802028	GCTGAAGAGGGTTAG[C/T]GAAACGTTAGCGGTC	10013
rs28711341	snp	G/T	0	0	intron-variant	HDAC6	GRCh38.p7	X:48808193	TGGGGTGTCCTGGTC[G/T]GGGCTCTTCCCCCAG	10013
rs34423449	in-del	-/A			intron-variant	HDAC6	GRCh38.p7	X:48810666	AGTCGTATTTGTGCC[-/A]CTGTACTCCAGTCTG	10013
rs34717743	in-del	-/T			intron-variant	HDAC6	GRCh38.p7	X:48810227	TTAGCTGGGTGTGGT[-/T]GGCACATGCCTGCAG	10013
rs34955786	snp	A/G	0	0	upstream-variant-2KB	HDAC6	GRCh38.p7	X:48800180	TGGTATTCTTTTGCA[A/G]GATTGAGGGTAGGGG	10013
rs34985248	in-del	-/C			frameshift-variant, nc-transcript-variant, intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48820248	AAAGTTACCTCTAGG[-/C]ATAAGGATAATGCGG	10013
rs34988126	in-del	-/C			intron-variant, upstream-variant-2KB	HDAC6	GRCh38.p7	X:48801497	CCAGTCACTTAGGAG[-/C]CCTTCGGGTCGGCGG	10013
rs35112134	in-del	-/T			upstream-variant-2KB	HDAC6	GRCh38.p7	X:48800243	TTGGCTTGAATGCCA[-/T]TAGTTTGCCGATCTG	10013
rs35306795	snp	A/T			upstream-variant-2KB	HDAC6	GRCh38.p7	X:48800328	CACATACGGTCTCAG[A/T]GGCATTTTTCTTTTT	10013
rs35738141	in-del	-/A			upstream-variant-2KB	HDAC6	GRCh38.p7	X:48801029	AGTTGCTGAACAGTT[-/A]CTGTGCTCCGTTTCC	10013
rs41298472	snp	A/T			intron-variant	HDAC6	GRCh38.p7	X:48817682	GGGCACTTACAAAAC[A/T]GGATCCAGGGTCCCA	10013
rs41310599	snp	A/C	0.0214859	0.101397	downstream-variant-500B, upstream-variant-2KB	HDAC6, ERAS	GRCh38.p7	X:48825106	CCATCCATTGCCCCC[A/C]AAAAACTAACTGAAA	10013
rs41312114	snp	A/G	0.00427135	0.0460155	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823730	GAGAGGCAGCTGGAG[A/G]TCAGGACATGGCTGA	10013
rs45441102	snp	C/T	0.0147244	0.0845304	intron-variant	HDAC6	GRCh38.p7	X:48803061	CCAAAGGTTCCCCAC[C/T]CTGGACAGTTCCCTC	10013
rs55842933	snp	A/G	0.0173306	0.0914601	intron-variant	HDAC6	GRCh38.p7	X:48805336	GACACCACAGTTTTG[A/G]GGTAAGCAGCTGTGG	10013
rs56747159	snp	A/G	0.0110639	0.0735497	intron-variant	HDAC6	GRCh38.p7	X:48817613	ACCCAGAGAAGGACC[A/G]AGGATGGAGCCTCTC	10013
rs57333741	snp	A/C/G	3.86294e-05	0.00439468	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48815428	AGGCGTCAGTGCTTC[A/C/G]CTCCACACCCTTCTG	10013
rs57466824	in-del	-/C			intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48815333	ATTATTATTATTCCC[-/C]TGGTCATGTCTGGTC	10013
rs57913011	snp	C/T			synonymous-codon, nc-transcript-variant, intron-variant	HDAC6	GRCh38.p7	X:48817403	CGGTTTTTGCTTTTT[C/T]AACTCTGTGGCTGTG	10013
rs61735967	snp	A/G/T	0.0499518	0.149936	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48822777	ATCGCAGATACTGGC[A/G/T]CAGCTTACGGGTCAT	10013
rs61737931	snp	C/T	0.0363512	0.129824	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48814457	TCCTCTATTTCTCCA[C/T]CCACCGCTACGAGCA	10013
rs73209760	snp	C/T	0.00357207	0.0421103	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	HDAC6	GRCh38.p7	X:48806443	CCTAGCAGACACCTA[C/T]GACTCAGTTTATCTG	10013
rs77316228	snp	C/T	0.5	0	intron-variant	HDAC6	GRCh38.p7	X:48810070	GGTTATCTTGGTGTT[C/T]TTTTTTTTTTTTTTT	10013
rs77409607	snp	G/T	0.5	0	intron-variant	HDAC6	GRCh38.p7	X:48810626	TTTATTTATTTTTTT[G/T]GAGACAAGGTCTTGC	10013
rs111255849	snp	A/G/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48819995	ATCTCTCTGACTTGC[A/G/T]TCTCCATGTCTTCAT	10013
rs111860068	snp	A/T			synonymous-codon, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48823156	CACAGGGGGAGCCAC[A/T]CTGGCCCAGACCATT	10013
rs112140048	snp	A/T			intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48807386	TTATAAAAATAAAAT[A/T]TTATTTTACACTAAC	10013
rs112427413	snp	C/T	0.5	0	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48808114	GGCAGCCCGCTATGC[C/T]CAACAGAAACACCGC	10013
rs113247595	snp	A/G	0.017851	0.0927731	intron-variant, utr-variant-3-prime, downstream-variant-500B	HDAC6	GRCh38.p7	X:48806108	GAAGAGGGTGACTGA[A/G]GGAAGGGAAGAACAG	10013
rs113573430	snp	A/C			intron-variant, upstream-variant-2KB	HDAC6	GRCh38.p7	X:48801698	GCGGTGTGGCTCAGC[A/C]CAGCTGGCGTAGCAC	10013
rs113585645	snp	A/G			intron-variant	HDAC6	GRCh38.p7	X:48816981	AGGTCCGGGCGTGAT[A/G]GCTCACACCTGTAAT	10013
rs113753590	snp	A/G	0.00158814	0.0281345	intron-variant	HDAC6	GRCh38.p7	X:48812203	CACACACAGATGTGA[A/G]ACACTGTGAATATAT	10013
rs116427806	snp	A/G	0.00896606	0.0663524	intron-variant	HDAC6	GRCh38.p7	X:48811516	AGTGTTTGTAGGTCT[A/G]TTTTCCTGAAAGGCA	10013
rs137925626	snp	C/T	0.00422943	0.0457911	upstream-variant-2KB	HDAC6	GRCh38.p7	X:48800113	CCCTGCCCATGAATC[C/T]CTGTCCTCACACACC	10013
rs138084502	snp	C/T	0.00448983	0.0471673	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823473	AAACTCCTCTAGCCT[C/T]GAGCACAGACCACCA	10013
rs138154887	snp	C/G	0.00942664	0.0680034	intron-variant	HDAC6	GRCh38.p7	X:48819923	TATTTCTTTTCTTCC[C/G]TTCTTCATTTTCAGT	10013
rs138420803	snp	A/G	0.00158814	0.0281345	intron-variant	HDAC6	GRCh38.p7	X:48809576	TTGGGAGGCCGAGGC[A/G]GATCACCTGAGGTCA	10013
rs138466917	snp	C/T	4.95577e-05	0.00497759	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48816239	TGACACCGCGCCCTG[C/T]CACAGAGGCTGAGCT	10013
rs139032847	snp	C/T	0.0168099	0.0901243	intron-variant	HDAC6	GRCh38.p7	X:48819025	AAAGGGTGTGAGCAC[C/T]GCTCTGTCACCCTGG	10013
rs139240691	snp	C/T			missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48822942	AAGGACCCTCCAGTT[C/T]TAAGTTGGTCACCAA	10013
rs139330641	snp	C/T	4.84966e-05	0.00492402	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48822776	CATCGCAGATACTGG[C/T]GCAGCTTACGGGTCA	10013
rs139655181	snp	C/T	0.00317376	0.039709	intron-variant	HDAC6	GRCh38.p7	X:48821957	GACTCCATCAGAGAG[C/T]CCAAGTTCAAACCCC	10013
rs139669611	snp	A/G	0.0772873	0.180749	intron-variant	HDAC6	GRCh38.p7	X:48814155	GTCTCTCACCAGAAC[A/G]TCTCCCTCAGCAAAC	10013
rs139742976	snp	C/T	0.0115877	0.0752302	intron-variant	HDAC6	GRCh38.p7	X:48803809	CATGAACAGATAATA[C/T]AGGTGAGGTTGGAAG	10013
rs139773351	snp	A/G	5.99251e-05	0.00547348	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48802921	TATCCCCAATCTAGC[A/G]GAGGTAAAGAAGAAA	10013
rs140347117	in-del	-/T			intron-variant	HDAC6	GRCh38.p7	X:48808226	TCACCTTGATCTCCT[-/T]GCACAGAGTCCCCTC	10013
rs141268593	snp	C/G/T	0.000265197	0.0115125	missense, nc-transcript-variant, intron-variant	HDAC6	GRCh38.p7	X:48802784	ACTCCAGTGTCACTT[C/G/T]GGTGAGGCCCTAGAC	10013
rs141405349	snp	C/T	0.00528398	0.051128	intron-variant, utr-variant-3-prime	HDAC6	GRCh38.p7	X:48806842	ATAATTAAAAATCTG[C/T]CTCCCATCCTTGTCA	10013
rs141406512	snp	C/T	2.38447e-05	0.00345279	synonymous-codon, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48823022	CGAGAAAAGAAGGTT[C/T]TGGAAGCAGGCATGG	10013
rs141467577	snp	A/G	0.000118887	0.00770903	synonymous-codon, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48814982	GATGGCCGCCACTCC[A/G]GCAGGGTTCGCCCAG	10013
rs141641633	snp	G/T	4.57509e-05	0.00478261	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48815634	TCTGGGAGGTTCTTG[G/T]GAGATCAAGTAGGAA	10013
rs141938903	snp	C/T	0.000623247	0.0176419	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48816207	GGAGCTGGGCCTTGC[C/T]GGGCGCTGCCTCACC	10013
rs142007727	snp	A/G	0.00707718	0.0590636	intron-variant	HDAC6	GRCh38.p7	X:48808177	TGGGGGTGGCATGGG[A/G]TGGGGTGTCCTGGTC	10013
rs142276149	snp	A/G	0.000140103	0.00836852	missense, nc-transcript-variant, utr-variant-3-prime	HDAC6	GRCh38.p7	X:48822669	TGGCTGCCTGCACTC[A/G]CTCCCTCCTTGGAGA	10013
rs142774634	snp	A/G	3.71581e-05	0.00431018	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823226	ACCTCAGAGGAGGCT[A/G]TCGGGGGAGCCACTC	10013
rs143030911	snp	C/T	0.00229762	0.0338162	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48823185	TTTCTGAGGCAGCCA[C/T]TGGGGGAGCCATGCT	10013
rs143074853	snp	C/T	0.01368	0.0815649	intron-variant	HDAC6	GRCh38.p7	X:48808380	CACCTCCCACCCTTA[C/T]AGGCCCAGCCAGAAG	10013
rs143480781	snp	A/G	0.00317376	0.039709	upstream-variant-2KB	HDAC6	GRCh38.p7	X:48800703	CTGTCAGTCTGATGC[A/G]GAACCCCCGGACTGC	10013
rs143498608	snp	C/T	0.00158814	0.0281345	intron-variant	HDAC6	GRCh38.p7	X:48817987	AGGGGTCTAGCCCAG[C/T]CCTCTTCCAGGGCGT	10013
rs143642817	snp	A/G	5.37844e-05	0.00518549	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823474	AACTCCTCTAGCCTC[A/G]AGCACAGACCACCAG	10013
rs143689285	snp	C/T	0.00728761	0.0599224	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48805666	AGAGCTGATGTTGGT[C/T]CACAGGTGAAGGCTT	10013
rs143759049	snp	A/G	5.77901e-05	0.0053751	synonymous-codon, intron-variant, nc-transcript-variant	HDAC6	GRCh38.p7	X:48818280	CCCCATGGGGGATGA[A/G]GGTGCCAGCAGCCAG	10013
rs144079643	in-del	-/A			intron-variant	HDAC6	GRCh38.p7	X:48812794	TTCTGTTTTCTTTTT[-/A]AACTTAGCTTGAGTG	10013
rs144699758	snp	A/G/T	0.00182387	0.0301473	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48824244	CTGGTCCTCAGCTAC[A/G/T]TCGACCTGTCAGCCT	10013
rs145147896	snp	A/G	0.00192692	0.0309798	synonymous-codon, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48823066	GGCATCATTTGGGGA[A/G]GAGTCCACTCCAGGC	10013
rs145152846	snp	C/T	0.00158814	0.0281345	intron-variant	HDAC6	GRCh38.p7	X:48818716	TGGATCTGTGTTGTA[C/T]GTGCGTGCCATCACA	10013
rs145223784	snp	C/G	8.20681e-05	0.00640526	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48815023	TGCTCATGGGTCTGG[C/G]AGGAGGCAAGCTGAT	10013
rs145263943	snp	A/G	0.016289	0.0887646	intron-variant	HDAC6	GRCh38.p7	X:48822287	CTGTATAGATTGAGC[A/G]CCTGTGGTTGTGAGG	10013
rs145349858	snp	C/G	0.000709384	0.0188199	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48802995	TCGTGGGACTGCAAG[C/G]GATGGTGAGCAGGGC	10013
rs145577593	snp	C/T	0.000529661	0.016265	intron-variant, utr-variant-3-prime	HDAC6	GRCh38.p7	X:48806814	TATATTCTCTTTTTT[C/T]CCTTTGGATTCTTGA	10013
rs145768118	snp	A/G	0.000452408	0.0150333	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	HDAC6	GRCh38.p7	X:48806665	CAGGCTGGTGGATGC[A/G]GTCCTGGGGGCTGAG	10013
rs145799176	snp	A/C	0.000189982	0.00974449	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48814563	CAATGTGCCTTGGAA[A/C]CAGGTCAGCATCTAC	10013
rs145874648	snp	A/G	0.000189982	0.00974449	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48823095	GCCAGACTAACTCAG[A/G]GACAGCTGTGGTGGC	10013
rs146047260	snp	C/T	0.00738971	0.0603345	intron-variant	HDAC6	GRCh38.p7	X:48805097	TGGGCATGGGTAATA[C/T]TTTGGCTTTTACTCA	10013
rs146616822	snp	A/T	2.4039e-05	0.00346683	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48822998	AGGTTAGCTGAGCGG[A/T]TGACCACACGAGAAA	10013
rs146634571	snp	C/T	0.000189982	0.00974449	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48814698	GCGGGATGCTGACTA[C/T]ATTGCTGCTTTCCTG	10013
rs146979948	snp	A/G	0.00190101	0.0307716	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823438	GTCAGAGGAGGCTCC[A/G]GGGGGCACCGAGCTG	10013
rs147012956	snp	C/T	0.00581083	0.0535878	intron-variant	HDAC6	GRCh38.p7	X:48807536	TTATTTATTTTGAGA[C/T]GGAGTCTCGCTCTGT	10013
rs147198199	snp	A/G	0.0256233	0.11025	intron-variant	HDAC6	GRCh38.p7	X:48822299	AGCGCCTGTGGTTGT[A/G]AGGATTGAGTTAATA	10013
rs147206457	snp	C/G			intron-variant	HDAC6	GRCh38.p7	X:48821718	TCACCATGTTGGCCA[C/G]GCTGGCCTCAAACTC	10013
rs147207522	snp	C/T	0.00110224	0.02345	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823571	CTCAGGACCTTGGAG[C/T]TAGGCAGCGAATCTC	10013
rs147285278	snp	A/G	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48821881	GGCTTGCAAAAAGTC[A/G]CACTTACTATGTGCC	10013
rs147417858	snp	C/T	7.17927e-05	0.00599092	synonymous-codon, nc-transcript-variant, intron-variant	HDAC6	GRCh38.p7	X:48817355	TGCTGTGGTGCGTCC[C/T]CCAGGACACCACGCA	10013
rs147420530	snp	C/T	0.000217834	0.0104341	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48802894	TATTAAAAAGGGAGC[C/T]GTTCCCCGCTCTATC	10013
rs147652236	snp	A/G	0.000814212	0.0201604	intron-variant, nc-transcript-variant	HDAC6	GRCh38.p7	X:48814749	CCTCGAGGTCCTGGG[A/G]ATCTGGGGTGTGTTG	10013
rs147854707	snp	A/C			upstream-variant-2KB	HDAC6	GRCh38.p7	X:48800643	GCGGCAGGACATCTT[A/C]AAGAGGATCAGAGGG	10013
rs147989097	snp	A/G	4.36119e-05	0.00466948	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48815417	GCCCTGGCTGAAGGC[A/G]TCAGTGCTTCGCTCC	10013
rs148220149	snp	C/G	0.00217788	0.0329271	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48823187	TCTGAGGCAGCCATT[C/G]GGGGAGCCATGCTGG	10013
rs148227458	snp	C/T	0.0168099	0.0901243	intron-variant	HDAC6	GRCh38.p7	X:48809024	CCTCTTAAAGTATCT[C/T]GTTCTTTGTAGTATT	10013
rs148527302	snp	C/T	0.00317376	0.039709	intron-variant	HDAC6	GRCh38.p7	X:48811886	TATCAACTCATTGGC[C/T]GATCTCATTTCATCT	10013
rs148529796	snp	A/G	0.000189982	0.00974449	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48824281	ACTACTGTCAGGCCT[A/G]TGTCCACCACCAGGT	10013
rs148657671	snp	A/T	0.000189982	0.00974449	missense, nc-transcript-variant, intron-variant	HDAC6	GRCh38.p7	X:48802778	CTCAGGACTCCAGTG[A/T]CACTTCGGTGAGGCC	10013
rs148707580	snp	A/G	0.000189982	0.00974449	synonymous-codon, nc-transcript-variant, intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48820189	CCAGGTGTCACCTGA[A/G]GGTTATGCCCACCTC	10013
rs148969792	snp	C/T	4.56897e-05	0.00477941	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48814467	CTCCATCCACCGCTA[C/T]GAGCAGGGTAGGTTC	10013
rs149286089	snp	A/G	4.8752e-05	0.00493696	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48816595	CAGCTTGCCACTGGC[A/G]CTGCCTGCCGCCTGG	10013
rs149349604	snp	G/T	0.000189982	0.00974449	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48823988	GTATGCCCCATACCT[G/T]CAGCAGGCCTAGACG	10013
rs149359047	snp	A/G	0.0282	0.115346	intron-variant	HDAC6	GRCh38.p7	X:48810463	TCATGCTTTTCTTAA[A/G]CTCTTGGAAATTATT	10013
rs149576597	snp	A/G	0.000231195	0.0107491	synonymous-codon, nc-transcript-variant, intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48820183	GGGCTGCCAGGTGTC[A/G]CCTGAGGGTTATGCC	10013
rs149727239	snp	A/G	0.000529661	0.016265	intron-variant, utr-variant-3-prime, downstream-variant-500B	HDAC6	GRCh38.p7	X:48806194	AGGGGAGCAGAGAAC[A/G]TTACCTGAACTGAGG	10013
rs149790381	snp	A/T	0.000307896	0.0124038	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	HDAC6	GRCh38.p7	X:48806644	CCTGGCCTCAGGCTC[A/T]GTCCTCAGGCTGGTG	10013
rs149901941	snp	C/G	0.000650618	0.0180246	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	HDAC6, ERAS	GRCh38.p7	X:48824876	GCAGCTCAGTGGCCC[C/G]AAGAGGGAGCTGATA	10013
rs150080446	snp	C/T	0.0529177	0.153813	intron-variant	HDAC6	GRCh38.p7	X:48816423	CAGGGAGGGGACAGA[C/T]CCTCCTCACTGTCCT	10013
rs150105386	snp	C/T	0.000745684	0.0192947	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48815933	CAATGTAGAGGAGAG[C/T]GAGGAGGAAGGACCC	10013
rs150446441	snp	C/T	0.00896606	0.0663524	intron-variant	HDAC6	GRCh38.p7	X:48809512	GGCCTTCAAAAAGTT[C/T]AGGATTTTAGGGCCG	10013
rs150537073	snp	A/G	0.00370173	0.0428621	upstream-variant-2KB	HDAC6	GRCh38.p7	X:48800747	CCCAGCTTATAGCCC[A/G]GTAGGAAATGGTGGA	10013
rs150815975	snp	A/G	0.00949095	0.0682305	intron-variant	HDAC6	GRCh38.p7	X:48819766	GCCAGGATGGTCTCA[A/G]TCTGACCTCATGATC	10013
rs150833052	snp	A/G			intron-variant	HDAC6	GRCh38.p7	X:48821691	TTTGTATTTTTAGTA[A/G]AGACGGGGGTTTCAC	10013
rs151130423	snp	A/G	0.0496864	0.149581	missense, upstream-variant-2KB, nc-transcript-variant	HDAC6, ERAS	GRCh38.p7	X:48824562	CTCCTAGATGTGAAG[A/G]ACATCGCCCACCAGA	10013
rs151262020	snp	A/G	0.000119643	0.00773351	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48822765	CCATCCAAGTCCATC[A/G]CAGATACTGGCGCAG	10013
rs151284143	snp	A/T	0.00456281	0.0475456	intron-variant, utr-variant-3-prime, nc-transcript-variant	HDAC6	GRCh38.p7	X:48805703	CTTGTAGGGATGGGG[A/T]GGAGCCTGCCCTGGA	10013
rs180839207	snp	C/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48804110	GAGGTTGCAGTGAGC[C/T]GAGATTGTGCCATTG	10013
rs181072984	snp	C/T	0.00317376	0.039709	downstream-variant-500B, upstream-variant-2KB	HDAC6, ERAS	GRCh38.p7	X:48825474	GCAGCTCAAGGGAGT[C/T]GGATCTGAGGTTTCC	10013
rs181156772	snp	C/G	0.00317376	0.039709	intron-variant	HDAC6	GRCh38.p7	X:48812517	CCAGAAAGGAAACTT[C/G]AGCTTATCTTGGGTG	10013
rs181434850	snp	C/T	0.00317376	0.039709	intron-variant	HDAC6	GRCh38.p7	X:48818679	GGCCTTCTGACTATG[C/T]ACCAATGGCCCGTGT	10013
rs181588627	snp	C/G/T	0.00422943	0.0457911	intron-variant	HDAC6	GRCh38.p7	X:48804920	ATTCTAGGCGGGGGT[C/G/T]GGGGGGCCAGCTAGA	10013
rs181600380	snp	C/T	0.000529661	0.016265	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	HDAC6, ERAS	GRCh38.p7	X:48824708	AGGGGTAGCCTCCCA[C/T]TGCATCCCATCCTGA	10013
rs182008482	snp	A/G	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48811474	GAAGGCCCATTGTAG[A/G]GGGCTGTCAGAGGAC	10013
rs182012626	snp	A/G	0.0131573	0.0800346	intron-variant	HDAC6	GRCh38.p7	X:48813129	GGCCATGCTGGTCTC[A/G]AACTTCTGGCCTCTA	10013
rs182026802	snp	C/T	3.0415e-05	0.00389956	intron-variant	HDAC6	GRCh38.p7	X:48803229	CAGGTGAGGCTGGGT[C/T]CTCCAGGCTGTCTCC	10013
rs182274491	snp	G/T	5.03455e-05	0.00501699	intron-variant, utr-variant-3-prime	HDAC6	GRCh38.p7	X:48806579	TGTTCTCTCCCTTAC[G/T]CCCTTTCTGGCTCCC	10013
rs182632183	snp	C/T	0.00105904	0.0229869	intron-variant	HDAC6	GRCh38.p7	X:48821919	GCTTGTGACAGGACA[C/T]GGTGGGAGTTAAGAA	10013
rs182847687	snp	A/G	5.15983e-05	0.00507902	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48814699	CGGGATGCTGACTAC[A/G]TTGCTGCTTTCCTGC	10013
rs182854777	snp	A/G	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48816331	GAGGTCTCAGGGGCT[A/G]GAACTTGGGTTTCCC	10013
rs182879167	snp	C/G	0.00317376	0.039709	intron-variant	HDAC6	GRCh38.p7	X:48821475	GGATTACAGGCATGA[C/G]CTACCATACCTGCCT	10013
rs183078461	snp	C/T	0.00422943	0.0457911	intron-variant	HDAC6	GRCh38.p7	X:48822458	ACAGTGGGTGCTGCC[C/T]ATCTTAAAGGTGTGG	10013
rs183507995	snp	C/T	0.00317376	0.039709	intron-variant	HDAC6	GRCh38.p7	X:48813821	CCCAGCCAGCACCCC[C/T]GCTCTAGTTCCACCC	10013
rs183744525	snp	A/T	0.000529661	0.016265	intron-variant, utr-variant-3-prime, downstream-variant-500B	HDAC6	GRCh38.p7	X:48806287	GGGAGCCAAGCCCTA[A/T]TTTGACCAGGGGGTT	10013
rs183986089	snp	C/T	0.0595685	0.161975	intron-variant, upstream-variant-2KB	HDAC6	GRCh38.p7	X:48801635	TTTACGTAGGCGCAG[C/T]ACAGCTGGCGTAGCA	10013
rs184188843	snp	A/G	0.00158814	0.0281345	upstream-variant-2KB	HDAC6	GRCh38.p7	X:48801208	AGACTCCTTCCACTC[A/G]GAATATTGCGGCAGA	10013
rs184473518	snp	C/G/T	0.000107026	0.00731448	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823748	AGGACATGGCTGATT[C/G/T]GATGCTGATGCAGGG	10013
rs184516070	snp	C/T	0	0	intron-variant	HDAC6	GRCh38.p7	X:48809366	TGAAGTGCTTGGAAC[C/T]AGAAGTATTTCACAT	10013
rs184587453	snp	G/T	0.00105904	0.0229869	intron-variant	HDAC6	GRCh38.p7	X:48818574	AGTTGGTGGCTGTGA[G/T]CACCTTGTGTATTTG	10013
rs184818576	snp	A/C/G	0.0007473	0.0193156	intron-variant	HDAC6	GRCh38.p7	X:48818028	GGTTACTGAGGTGCT[A/C/G]TCTCCTCCCCAGGAT	10013
rs185029301	snp	C/T	0.00211696	0.0324653	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48807061	CAGTATTTTCTGCTT[C/T]GTTTTTGGCATGTAA	10013
rs185259735	snp	A/G	0.0115877	0.0752302	intron-variant	HDAC6	GRCh38.p7	X:48813945	CTTAGCTGGCTCCCC[A/G]CAGCTAAGAGCCCCA	10013
rs185304271	snp	A/G			intron-variant	HDAC6	GRCh38.p7	X:48804168	ACTCTGTCTCAAAAA[A/G]TAAAAATAAAAAAAA	10013
rs185396570	snp	A/G	0.00105904	0.0229869	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	HDAC6, ERAS	GRCh38.p7	X:48824857	AGCCCAGAAGGAAAG[A/G]GGGGCAGCTCAGTGG	10013
rs185742263	snp	G/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48803636	ACTGAAACAGAAGGA[G/T]GAAACCTCCCGTTTG	10013
rs185991355	snp	C/T	0.000529661	0.016265	downstream-variant-500B, upstream-variant-2KB	HDAC6, ERAS	GRCh38.p7	X:48825346	CAGGTTTAACTTGAA[C/T]GTGGTGGTCATGGTA	10013
rs186020965	snp	C/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48818736	GTGCCATCACAAGTG[C/T]TTGAGTATGTGCGTG	10013
rs186106679	snp	A/G	0.00317376	0.039709	intron-variant	HDAC6	GRCh38.p7	X:48821481	CAGGCATGAGCTACC[A/G]TACCTGCCTCTTTTT	10013
rs186261418	snp	A/G	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48813660	CAAAACACGTGCATC[A/G]CATCTTTTCAGTATC	10013
rs186499554	snp	A/G	9.90921e-05	0.0070382	missense, nc-transcript-variant, intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48820236	GCCTTGCCAGTGGCC[A/G]CATTATCCTTATCCT	10013
rs186653243	snp	A/G	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48805224	CGAAGCAGGGAGGCC[A/G]AGGAGATGCCGCCAC	10013
rs186655863	snp	C/G	0.00317376	0.039709	intron-variant	HDAC6	GRCh38.p7	X:48812520	GAAAGGAAACTTCAG[C/G]TTATCTTGGGTGCCC	10013
rs186664222	snp	C/T	0.00211696	0.0324653	upstream-variant-2KB	HDAC6	GRCh38.p7	X:48801214	CTTCCACTCAGAATA[C/T]TGCGGCAGAATATTA	10013
rs187221799	snp	C/T	0.00186422	0.0304735	splice-donor-variant, upstream-variant-2KB	HDAC6	GRCh38.p7	X:48801946	CAATGAGTGGAGCGG[C/T]GAGTACAGCGCGTCG	10013
rs187310327	snp	A/C	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48822404	TATTGTTATCTTGCA[A/C]TTTACATCACAATTT	10013
rs187528998	snp	C/T	0.0068637	0.0581785	intron-variant	HDAC6	GRCh38.p7	X:48816857	CTGTAATCCTAGCGC[C/T]TTGAGAAGCTGAGGT	10013
rs188029286	snp	G/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48803890	AAGGAGGCCAGGCAT[G/T]GTGGCTCACGCCTAT	10013
rs188229605	snp	G/T			intron-variant	HDAC6	GRCh38.p7	X:48807703	ATTTTTAGTAGAGAC[G/T]GGGTTTCACCGTGTT	10013
rs188264171	snp	A/G	0.000147258	0.00857947	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48815487	CTGGTGCCCCCTGCC[A/G]GAGGTGAGCCCCGGT	10013
rs188815681	snp	A/G	0.000529661	0.016265	upstream-variant-2KB	HDAC6	GRCh38.p7	X:48800108	CCTGACCCTGCCCAT[A/G]AATCCCTGTCCTCAC	10013
rs188950679	snp	A/C/T	7.73681e-05	0.00621925	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	HDAC6, ERAS	GRCh38.p7	X:48824624	CTAAGCCCCAGAATA[A/C/T]GGTCCCTCTTCACCT	10013
rs189064885	snp	C/T	0.000625617	0.0176753	intron-variant	HDAC6	GRCh38.p7	X:48818438	GGATAGATCGCAGGA[C/T]GTATGTGACACGCCT	10013
rs189092231	snp	A/G			missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823349	ACTACCTCAGAGGAG[A/G]CTGTAGGAGGAGCTA	10013
rs189213724	snp	C/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48819189	GTGGCTGTGTGGTGA[C/T]GGCATGTGTATGTGA	10013
rs189292324	snp	C/T	2.57099e-05	0.00358529	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48823819	TGGGACTGTGGCTTC[C/T]TTCTCTTGCCAATTT	10013
rs189351993	snp	A/T	0.0312828	0.12109	intron-variant	HDAC6	GRCh38.p7	X:48810618	TTTATTTATTTATTT[A/T]TTTTTTTTGAGACAA	10013
rs189565038	snp	C/T	0.00422943	0.0457911	intron-variant	HDAC6	GRCh38.p7	X:48811566	GGGAATGTCCACTGA[C/T]AGGTTGCAACTTTAG	10013
rs189690352	snp	G/T	0.000529661	0.016265	intron-variant, utr-variant-3-prime	HDAC6	GRCh38.p7	X:48806538	TGCCCACCCCACCCT[G/T]GGGGAAGCAGCTGAG	10013
rs189804555	snp	C/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48812619	ATTCATTGAAGTCTC[C/T]TATTCTCTGACATCC	10013
rs189811906	snp	A/G	0.00317376	0.039709	intron-variant	HDAC6	GRCh38.p7	X:48818597	TGTATTTGTGCACAG[A/G]TGGCTGTACATGACT	10013
rs189848954	snp	G/T	0.00896606	0.0663524	downstream-variant-500B, upstream-variant-2KB	HDAC6, ERAS	GRCh38.p7	X:48825452	CCACGTGGTGAGAAT[G/T]GCTTTGGCAGCTCAA	10013
rs190069123	snp	A/G	0.00105904	0.0229869	intron-variant	HDAC6	GRCh38.p7	X:48804887	GGAGTAAGTCATGGA[A/G]ACAGTTGGAGGAAGA	10013
rs190360216	snp	C/T	0.00148748	0.027231	intron-variant	HDAC6	GRCh38.p7	X:48803118	GTCTCCTTTTTTTTT[C/T]CCTCTGCAGGATCTG	10013
rs190590343	snp	C/T			downstream-variant-500B, upstream-variant-2KB	HDAC6, ERAS	GRCh38.p7	X:48825038	CCTGGCCAGCAGAGC[C/T]GATGAGTAATGAAGG	10013
rs190591847	snp	C/T	0.00158814	0.0281345	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48820419	CATTAACAGCCTTAA[C/T]TGAGTGCTCACTATG	10013
rs191034995	snp	A/C			intron-variant	HDAC6	GRCh38.p7	X:48813798	CCTTTCACTGGCCTC[A/C]TGACAGCCCCAGCCA	10013
rs191082746	snp	A/C	0.00393213	0.0441656	intron-variant	HDAC6	GRCh38.p7	X:48814609	AAGTGAGGCCCAGCC[A/C]CGCCCTTCTGTCAGC	10013
rs191407208	snp	A/G	0.00158814	0.0281345	intron-variant	HDAC6	GRCh38.p7	X:48821632	ATGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC	10013
rs191513880	snp	C/T	0.00105904	0.0229869	intron-variant, upstream-variant-2KB	HDAC6	GRCh38.p7	X:48801462	CTAATTCCCTCGCTT[C/T]CTTGCTTGCTCTCCA	10013
rs191735691	snp	A/G	0.000140469	0.00837943	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48824108	GGCGGAGGTTGGCCC[A/G]GGAGCAAACTGCAGG	10013
rs191943015	snp	A/G	0.00791544	0.0624105	intron-variant	HDAC6	GRCh38.p7	X:48805358	CAGCTGTGGAAGGGT[A/G]GATGGGGAGATGTGG	10013
rs191952249	snp	A/G	0.00105904	0.0229869	upstream-variant-2KB	HDAC6	GRCh38.p7	X:48800253	AAACTATGGCATTCA[A/G]GCCAAAGCCAGACTG	10013
rs192190191	snp	C/T			intron-variant	HDAC6	GRCh38.p7	X:48822437	TCCCCACAACAACCA[C/T]CTTACACAGTGGGTG	10013
rs192642275	snp	G/T	0.000152884	0.00874178	intron-variant, utr-variant-3-prime	HDAC6	GRCh38.p7	X:48806737	ATTTGACTTTTTACA[G/T]TGTTTTAAAGTCCTT	10013
rs192721188	snp	C/G	0.00317376	0.039709	intron-variant	HDAC6	GRCh38.p7	X:48818530	ATGATATGAGACAGC[C/G]CATGGGTGTTTAATG	10013
rs192998875	snp	A/G	0.00179171	0.0298772	intron-variant, upstream-variant-2KB	HDAC6	GRCh38.p7	X:48802643	CCCTCACATACCCAC[A/G]CTCCTCCCCCCACCC	10013
rs193174757	snp	C/T			intron-variant	HDAC6	GRCh38.p7	X:48809073	TCTGGTTATTTAACC[C/T]CAGGACTTTTAAGAT	10013
rs199501353	snp	A/G	0.000343966	0.0131097	missense, utr-variant-3-prime, nc-transcript-variant	HDAC6	GRCh38.p7	X:48806393	ATTGATCTGATGGAA[A/G]CAACCCAGTACATGA	10013
rs199503400	snp	A/G	0.000155067	0.00880394	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48823814	GAGGCTGGGACTGTG[A/G]CTTCCTTCTCTTGCC	10013
rs199513877	snp	A/G	5.16142e-05	0.00507981	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48822929	GTAGAAGACAGAGAA[A/G]GACCCTCCAGTTCTA	10013
rs199596944	snp	A/G	0.000171766	0.00926573	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48822786	ACTGGCGCAGCTTAC[A/G]GGTCATGAGTGAGTG	10013
rs199882300	snp	A/G	0.000175753	0.0093726	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48808070	CACAGTCTTATGGAT[A/G]GCTATTGCATGTTCA	10013
rs199900920	snp	A/G	0.000487975	0.0156125	intron-variant	HDAC6	GRCh38.p7	X:48814432	ACCTCTTTTTCTTCT[A/G]CCCCCAGTGTCCTCT	10013
rs199985595	snp	A/G	2.35693e-05	0.0034328	intron-variant	HDAC6	GRCh38.p7	X:48814577	ACCAGGTCAGCATCT[A/G]CCCACCTCTGCCCCC	10013
rs200011702	in-del	-/C	0.0166897	0.0898126	intron-variant	HDAC6	GRCh38.p7	X:48824332	ACACGTGCACACTCA[-/C]CCCCCCACACACACA	10013
rs200111431	snp	A/G/T	0.000276328	0.0117511	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48823146	CAGAGGCAGCCACAG[A/G/T]GGGAGCCACTCTGGC	10013
rs200220866	snp	A/G	2.92851e-05	0.00382645	missense, intron-variant, nc-transcript-variant	HDAC6	GRCh38.p7	X:48818401	CGCCTGGTGCTTCCC[A/G]TTGCCTACGAGGTAC	10013
rs200470948	snp	A/G	0.000529661	0.016265	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48823805	GCTCAGGGAGAGGCT[A/G]GGACTGTGGCTTCCT	10013
rs200472671	snp	C/T	0.00018609	0.00964418	intron-variant	HDAC6	GRCh38.p7	X:48820071	CCAAAAGCCCCTACC[C/T]TCATGCTTATACATC	10013
rs200608395	snp	C/T	0.000381335	0.013803	intron-variant, utr-variant-3-prime, downstream-variant-500B	HDAC6	GRCh38.p7	X:48806321	GTATGGACAGCTCAG[C/T]TGGGGAAGAGACAGG	10013
rs200639202	snp	A/G	0.000168728	0.00918343	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48822996	CTAGGTTAGCTGAGC[A/G]GATGACCACACGAGA	10013
rs200729544	in-del	-/GGGCTG			intron-variant	HDAC6	GRCh38.p7	X:48815729	TCCTCTGACTTTACT[-/GGGCTG]CCTTGGTGGGAGAGG	10013
rs200736457	snp	A/C	0.000512445	0.0159987	intron-variant	HDAC6	GRCh38.p7	X:48824339	GCACACTCACCCCCC[A/C]CACACACACCCCTTC	10013
rs201041789	snp	C/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48814406	TGGGGATTGACTTCT[C/T]CAACTCTCTTACCTC	10013
rs201090076	snp	C/T	0.000165332	0.00909059	intron-variant	HDAC6	GRCh38.p7	X:48814583	TCAGCATCTACCCAC[C/T]TCTGCCCCCAAAGTG	10013
rs201209428	snp	C/T	0.000529661	0.016265	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48815338	TTATTATTCCCTGGT[C/T]ATGTCTGGTCCTTTC	10013
rs201216577	snp	C/T	0.00355279	0.0419973	intron-variant	HDAC6	GRCh38.p7	X:48816101	GGGGGTCCCTCCCCC[C/T]CAGGCACTAAGCCTC	10013
rs201220462	snp	A/G	0.000801462	0.0200022	intron-variant	HDAC6	GRCh38.p7	X:48823634	GAAGGGGCAAGAATC[A/G]GGCTTCTCTGATACA	10013
rs201520385	snp	A/G	0.000216237	0.0103957	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48815892	CTTTTAGCTGAGACC[A/G]TGGAGAGGGACAACA	10013
rs201526063	snp	A/G	8.26868e-05	0.00642935	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48805474	GCTCCATGCCATCAA[A/G]GAGCAACTGATCCAG	10013
rs201701559	snp	A/G	0.000529661	0.016265	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48824126	AGCAAACTGCAGGGG[A/G]ATGCTGACCCCCACC	10013
rs201822204	snp	C/T	0.000529661	0.016265	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	HDAC6	GRCh38.p7	X:48806617	TCTCCAGAACTCATA[C/T]TCCTGTGCCTGCCTG	10013
rs201823919	snp	C/T	0.000104745	0.00723612	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48808312	AACACAGTTCACCTT[C/T]GACCAGGACCCCAGG	10013
rs201845777	snp	C/T	0.000241493	0.0109858	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48822995	CCTAGGTTAGCTGAG[C/T]GGATGACCACACGAG	10013
rs202031097	snp	C/T	3.08043e-05	0.00392444	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48802901	AAGGGAGCCGTTCCC[C/T]GCTCTATCCCCAATC	10013
rs202088206	snp	A/G	0.000529661	0.016265	synonymous-codon, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48815036	GGCAGGAGGCAAGCT[A/G]ATCCTGTCTCTGGAG	10013
rs202245023	snp	A/G	0.000100393	0.00708423	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48803151	CCTTGAGGCTGAAGC[A/G]CTGGCTGGCACTGGC	10013
rs367581386	snp	A/G	0.000141972	0.00842413	intron-variant	HDAC6	GRCh38.p7	X:48818450	GGACGTATGTGACAC[A/G]CCTGTGCAGGTGGCA	10013
rs367764976	snp	C/T	4.10914e-05	0.00453255	intron-variant	HDAC6	GRCh38.p7	X:48805395	CAGATGTGGAGCTCC[C/T]CAGTGTCCTCATGCA	10013
rs367767249	snp	A/G	0.000622471	0.0176309	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823531	AACTACACCCCAGAT[A/G]TCTCCCAGTACACTG	10013
rs367787331	snp	G/T	2.29529e-05	0.00338761	intron-variant	HDAC6	GRCh38.p7	X:48816104	GGTCCCTCCCCCTCA[G/T]GCACTAAGCCTCTAC	10013
rs367939546	snp	A/G	4.34991e-05	0.00466344	missense, intron-variant, nc-transcript-variant	HDAC6	GRCh38.p7	X:48818303	GCAGCCAGATCGGCC[A/G]GGCTGCGGGCACAGG	10013
rs368035005	snp	G/T			intron-variant	HDAC6	GRCh38.p7	X:48807882	GCAGGGGGTGAGAGT[G/T]TGAGGGCCTCCATTA	10013
rs368186562	snp	A/G	0.000849815	0.0205958	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823450	TCCAGGGGGCACCGA[A/G]CTGATCCAAACTCCT	10013
rs368341039	snp	C/T	0.0003938	0.0140266	synonymous-codon, nc-transcript-variant, missense	HDAC6	GRCh38.p7	X:48818071	TTGGGATGTCCACCA[C/T]GGTAATGGAACTCAG	10013
rs368394917	snp	A/C	0.000987793	0.0222018	intron-variant	HDAC6	GRCh38.p7	X:48808146	TCCGGAGGTCAGCAA[A/C]AGAGGGCAGATGTGA	10013
rs368570596	snp	A/G	2.75824e-05	0.00371355	intron-variant	HDAC6	GRCh38.p7	X:48824500	AGCCGAGGTAGAGGG[A/G]TCCTCACTCTCTCTC	10013
rs368581451	snp	C/T			intron-variant, upstream-variant-2KB	HDAC6	GRCh38.p7	X:48801851	AATGGAAAAGAAAAG[C/T]CTGAGCGCTCGCGTC	10013
rs368582393	snp	C/T	2.28762e-05	0.00338195	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48815608	CTGTGCTCTGGAAGC[C/T]CTTGAGCCCTTCTGG	10013
rs368591849	snp	C/T	2.95016e-05	0.00384056	intron-variant	HDAC6	GRCh38.p7	X:48805541	AGGCCCCCAAGCCAA[C/T]ACTCTGGGTGAAGGG	10013
rs368756519	snp	C/T	2.95051e-05	0.00384079	intron-variant	HDAC6	GRCh38.p7	X:48823600	TCAGGTAAGGCTCAC[C/T]ACACCCAGGTAGGGG	10013
rs368804563	snp	A/G	2.40807e-05	0.00346984	intron-variant	HDAC6	GRCh38.p7	X:48824322	TAGACCCTTCGACAC[A/G]TGCACACTCACCCCC	10013
rs368853977	snp	C/T	0.00475684	0.0485365	intron-variant, upstream-variant-2KB	HDAC6	GRCh38.p7	X:48801561	GGACGACAGCGACGA[C/T]AGCCGAGGCAAGAAA	10013
rs368947624	snp	A/G			intron-variant	HDAC6	GRCh38.p7	X:48810180	TCCTGGGCTCAAGCA[A/G]TCCTCCTGCCTCAGC	10013
rs368982507	snp	A/G	5.02525e-05	0.00501236	intron-variant, utr-variant-3-prime, downstream-variant-500B	HDAC6	GRCh38.p7	X:48806336	TTGGGGAAGAGACAG[A/G]GCCCTGAATCTCATC	10013
rs368986528	snp	C/T	9.44629e-05	0.00687186	intron-variant	HDAC6	GRCh38.p7	X:48823663	CATCTCTTACTTCTG[C/T]GTGTCCAGGGGGCCT	10013
rs369005856	snp	C/T	0.000136922	0.00827299	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48814491	TAGGTTCTGGCCCCA[C/T]CTGAAGGCCTCTAAC	10013
rs369151284	snp	A/G/T	0.000157952	0.00888564	intron-variant	HDAC6	GRCh38.p7	X:48808336	CCCCAGGTATACCCC[A/G/T]ACTCCCACCTAGGTG	10013
rs369193053	snp	G/T			upstream-variant-2KB	HDAC6	GRCh38.p7	X:48801004	TATTATTATCACAAC[G/T]TTCCAGATGAGGAAA	10013
rs369292868	snp	A/G	6.7193e-05	0.00579586	missense, utr-variant-5-prime, nc-transcript-variant, intron-variant	HDAC6	GRCh38.p7	X:48802676	AGAACCGCGGCAGGG[A/G]CCAAGCCTCCTCAAC	10013
rs369431391	snp	A/G	0.000549127	0.0165609	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48822839	CCCAGGGAAGGAGGG[A/G]GCTGAGGGGCAGAGA	10013
rs369651408	snp	G/T	5.56793e-05	0.00527604	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48820269	AGGTAACTTTCTCTT[G/T]GTCCCTCTTCCCACA	10013
rs369700028	snp	C/T	0.000356103	0.0133388	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48814716	TGCTGCTTTCCTGCA[C/T]GTCCTGCTGCCAGTC	10013
rs369889565	snp	C/T	0.000189982	0.00974449	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	HDAC6	GRCh38.p7	X:48806452	CACCTACGACTCAGT[C/T]TATCTGCATCCGGTA	10013
rs369905433	snp	C/T	2.28809e-05	0.0033823	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48816186	GCGGATCATGTGCCG[C/T]CTGGAGGAGCTGGGC	10013
rs369996405	snp	A/G/T	6.57343e-05	0.00573261	intron-variant	HDAC6	GRCh38.p7	X:48802816	CGCCCTGATGAGGGG[A/G/T]AGAGGGAGCAAGTTG	10013
rs370045870	snp	C/T			intron-variant	HDAC6	GRCh38.p7	X:48815873	GGACAAACGTGGCCT[C/T]CCCCTTTTAGCTGAG	10013
rs370065570	snp	C/T	2.30603e-05	0.00339553	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48823909	CTTACCTAGTTTCAC[C/T]CACCCACTCCAGGCC	10013
rs370302680	snp	A/G	3.2817e-05	0.00405061	intron-variant	HDAC6	GRCh38.p7	X:48817283	AAGGAAGAAAGGAAG[A/G]TGAGGGCAGGCTGTC	10013
rs370312010	snp	A/G	5.44321e-05	0.00521662	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48815402	GGCTACAACCTCCGC[A/G]CCCTGGCTGAAGGCG	10013
rs370388702	snp	A/G	0.000189982	0.00974449	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48824110	CGGAGGTTGGCCCGG[A/G]AGCAAACTGCAGGGG	10013
rs370628443	snp	A/G	5.34295e-05	0.00516836	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48814952	AGGCTGACCCTCCAT[A/G]TCCCCCCAGGGTGAG	10013
rs370633029	snp	C/T			intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48820640	AGCCTGGCTCCAGGG[C/T]TTGTGCTTTTTACTC	10013
rs370785726	snp	A/G	0.000160278	0.0089506	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823510	CCCAACCTCACCTGT[A/G]CAGGGAACTACACCC	10013
rs370824933	snp	C/T	2.50674e-05	0.00354021	intron-variant, utr-variant-3-prime	HDAC6	GRCh38.p7	X:48806584	TCTCCCTTACTCCCT[C/T]TCTGGCTCCCCACTG	10013
rs370891084	snp	A/G	0.000189982	0.00974448	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823229	TCAGAGGAGGCTGTC[A/G]GGGGAGCCACTCCGG	10013
rs370900424	snp	A/G	0.000189982	0.00974449	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48824079	ATCAGGTATGGAGCA[A/G]AGGAAGGGGATGGGG	10013
rs371051191	snp	C/T	0.000571628	0.0168964	intron-variant	HDAC6	GRCh38.p7	X:48818131	GCTGCAGTCAGGGGC[C/T]GCAGTGTGATCAGGG	10013
rs371304801	snp	A/G	0.000164645	0.00907169	intron-variant	HDAC6	GRCh38.p7	X:48803032	GCAGTTTAGCCTCGT[A/G]TGACAATCAAAACCC	10013
rs371445841	snp	A/G			synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823243	CGGGGGAGCCACTCC[A/G]GACCAGACCACCTCA	10013
rs371474323	snp	C/T	0.0220041	0.102557	intron-variant	HDAC6	GRCh38.p7	X:48808632	TATTCACTGATTAAC[C/T]GTTGGGTTAGAGTGA	10013
rs371507088	snp	A/G	0.000189982	0.00974449	intron-variant	HDAC6	GRCh38.p7	X:48805406	CTCCCCAGTGTCCTC[A/G]TGCATCTGTGACTGT	10013
rs371512851	snp	A/G	0.000773043	0.0196449	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823552	CAGTACACTGATTGG[A/G]AGTCTCAGGACCTTG	10013
rs371640761	snp	A/G	0.000124046	0.0078745	intron-variant, utr-variant-3-prime, nc-transcript-variant	HDAC6	GRCh38.p7	X:48805705	TGTAGGGATGGGGAG[A/G]AGCCTGCCCTGGACA	10013
rs371757079	snp	G/T	0.000189982	0.00974449	intron-variant	HDAC6	GRCh38.p7	X:48816105	GTCCCTCCCCCTCAG[G/T]CACTAAGCCTCTACC	10013
rs371819184	snp	A/G	2.44529e-05	0.00349655	missense, upstream-variant-2KB, nc-transcript-variant	HDAC6, ERAS	GRCh38.p7	X:48824580	ATCGCCCACCAGAAC[A/G]AGTTTGGGGAGGATA	10013
rs371994740	snp	C/T			intron-variant	HDAC6	GRCh38.p7	X:48811579	GACAGGTTGCAACTT[C/T]AGCGAGTGTGGGCAA	10013
rs372000801	snp	C/T	0.000253328	0.0112517	intron-variant	HDAC6	GRCh38.p7	X:48815678	CTGGTGTGGGGTGGA[C/T]GTGGGATGAGCCCTG	10013
rs372128626	snp	A/C	0.000189982	0.00974449	intron-variant	HDAC6	GRCh38.p7	X:48823618	ACCCAGGTAGGGGCA[A/C]GAAGGGGCAAGAATC	10013
rs372334849	snp	A/G	7.80229e-05	0.00624543	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48808054	TGGACATCACGCCCA[A/G]CACAGTCTTATGGAT	10013
rs372435098	snp	C/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48809662	GAAAAATTAGCCAGG[C/T]GTGGTGGCACACACC	10013
rs372464158	snp	A/G	2.67151e-05	0.0036547	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823749	GGACATGGCTGATTC[A/G]ATGCTGATGCAGGGA	10013
rs372471896	snp	A/C	0.000411918	0.0143454	missense, utr-variant-3-prime, nc-transcript-variant	HDAC6	GRCh38.p7	X:48806405	GAAACAACCCAGTAC[A/C]TGAATGAGGGAGAAC	10013
rs372611311	snp	A/C	3.12867e-05	0.00395504	intron-variant	HDAC6	GRCh38.p7	X:48805569	GGGCAGGGAGCTGAC[A/C]TGACCTGGGTGCAGC	10013
rs372636491	snp	C/G	0.000409291	0.0142996	synonymous-codon, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48822937	CAGAGAAGGACCCTC[C/G]AGTTCTAAGTTGGTC	10013
rs372651111	snp	C/T	6.49266e-05	0.00569729	synonymous-codon, utr-variant-5-prime, nc-transcript-variant, intron-variant	HDAC6	GRCh38.p7	X:48802677	GAACCGCGGCAGGGG[C/T]CAAGCCTCCTCAACT	10013
rs372770967	snp	C/T	2.3228e-05	0.00340785	intron-variant	HDAC6	GRCh38.p7	X:48820073	AAAAGCCCCTACCCT[C/T]ATGCTTATACATCTC	10013
rs372814071	snp	C/G	2.4362e-05	0.00349005	intron-variant	HDAC6	GRCh38.p7	X:48824338	TGCACACTCACCCCC[C/G]ACACACACACCCCTT	10013
rs372936089	snp	C/G	0.000189982	0.00974449	intron-variant	HDAC6	GRCh38.p7	X:48816455	CGGGTGCTCCTCTCT[C/G]TGCTTCCAGTGCTGA	10013
rs373004163	snp	C/T	5.88426e-05	0.00542382	intron-variant	HDAC6	GRCh38.p7	X:48817299	TGAGGGCAGGCTGTC[C/T]GATCTTAGCACCCTG	10013
rs373100563	snp	C/T	0.000575834	0.0169583	intron-variant, upstream-variant-2KB	HDAC6	GRCh38.p7	X:48802642	CCCCTCACATACCCA[C/T]GCTCCTCCCCCCACC	10013
rs373102129	snp	A/G			intron-variant	HDAC6	GRCh38.p7	X:48818448	CAGGACGTATGTGAC[A/G]CGCCTGTGCAGGTGG	10013
rs373313895	snp	A/G	2.28613e-05	0.00338085	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48824028	CTTGTGGGGACTGTG[A/G]AACAATCCAAGAGAA	10013
rs373431660	snp	A/G	0.000189982	0.00974449	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48814539	CGGCCAAGGCCAAGG[A/G]TATACCATCAATGTG	10013
rs373500301	snp	A/G	0.00844089	0.0644143	intron-variant	HDAC6	GRCh38.p7	X:48817187	AACCTGGCAGGCGGC[A/G]CTTGCAGTGAGCCGA	10013
rs373500924	snp	A/C/G	9.61888e-05	0.00693446	intron-variant	HDAC6	GRCh38.p7	X:48802849	CATGCCCTGGACTCT[A/C/G]ACCCTTCTCTCTGAT	10013
rs373502965	snp	A/G	2.39017e-05	0.00345692	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48823037	CTGGAAGCAGGCATG[A/G]GGAAAGTCACCTCGG	10013
rs373588692	snp	C/T	5.06611e-05	0.00503269	intron-variant	HDAC6	GRCh38.p7	X:48822573	TGTCCTCCAAATTCC[C/T]CAATGAACCCCCACC	10013
rs373689994	snp	C/T	0.000219416	0.0104719	intron-variant, utr-variant-3-prime	HDAC6	GRCh38.p7	X:48806606	TCCCCACTGTCTCTC[C/T]AGAACTCATACTCCT	10013
rs373742148	snp	A/G	0.000189982	0.00974449	intron-variant, utr-variant-3-prime	HDAC6	GRCh38.p7	X:48806484	GGATGAGAACTCTGC[A/G]GGCAGGGAATGGTGG	10013
rs374088297	snp	C/T	8.91822e-05	0.00667706	missense, intron-variant, nc-transcript-variant	HDAC6	GRCh38.p7	X:48818302	AGCAGCCAGATCGGC[C/T]GGGCTGCGGGCACAG	10013
rs374215726	snp	A/G	0.000164865	0.00907773	intron-variant	HDAC6	GRCh38.p7	X:48803042	CTCGTATGACAATCA[A/G]AACCCAAAGGTTCCC	10013
rs374265406	snp	A/G	2.39123e-05	0.00345768	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48816225	GCGCTGCCTCACCCT[A/G]ACACCGCGCCCTGCC	10013
rs374272352	snp	A/G	0.000115145	0.00758678	intron-variant	HDAC6	GRCh38.p7	X:48815679	TGGTGTGGGGTGGAC[A/G]TGGGATGAGCCCTGG	10013
rs374293695	snp	C/T	0.022522	0.1037	intron-variant	HDAC6	GRCh38.p7	X:48821136	AGCCACCGCACCTGG[C/T]CCCTGGTTACTGTTA	10013
rs374453711	snp	C/T	8.73134e-05	0.00660674	intron-variant	HDAC6	GRCh38.p7	X:48818000	AGCCCTCTTCCAGGG[C/T]GTGAGTATCGTCGGT	10013
rs374499408	snp	A/C	0.000255114	0.0112912	intron-variant	HDAC6	GRCh38.p7	X:48823648	CGGGCTTCTCTGATA[A/C]ATCTCTTACTTCTGC	10013
rs374583816	snp	A/G	3.11813e-05	0.00394838	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48814992	ACTCCGGCAGGGTTC[A/G]CCCAGCTAACCCACC	10013
rs374641083	snp	C/T	8.92957e-05	0.00668131	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48815416	CGCCCTGGCTGAAGG[C/T]GTCAGTGCTTCGCTC	10013
rs374838428	snp	C/T	4.79662e-05	0.00489702	intron-variant	HDAC6	GRCh38.p7	X:48824316	CCTGGGTAGACCCTT[C/T]GACACGTGCACACTC	10013
rs374881662	snp	G/T			intron-variant	HDAC6	GRCh38.p7	X:48813762	GAGGTGGCCTGTAAG[G/T]CATTGGGGAGGAGGA	10013
rs374888007	snp	C/T	3.17163e-05	0.0039821	intron-variant	HDAC6	GRCh38.p7	X:48823655	CTCTGATACATCTCT[C/T]ACTTCTGCGTGTCCA	10013
rs374906898	snp	C/G	0.000883609	0.0210006	intron-variant	HDAC6	GRCh38.p7	X:48814388	TTGGGTTGGGGGTGT[C/G]TATGGGGATTGACTT	10013
rs374985832	in-del	-/GTT			intron-variant	HDAC6	GRCh38.p7	X:48820851	GTTGTTGTTGTTGTT[-/GTT]TGTGAGACAAGAGTC	10013
rs375017709	snp	A/T	0.000189982	0.00974449	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48808305	GTCAAGGAACACAGT[A/T]CACCTTCGACCAGGA	10013
rs375071316	snp	A/G	0.000189982	0.00974448	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823515	CCTCACCTGTGCAGG[A/G]AACTACACCCCAGAT	10013
rs375080531	snp	A/C	0.000111997	0.00748237	intron-variant	HDAC6	GRCh38.p7	X:48803265	ACAAAAATACACACA[A/C]TTAGAGCCCATTAGC	10013
rs375135223	snp	C/T	0.00105904	0.0229869	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48807251	ATGTATCTTGGAGCC[C/T]GGTAGAACACCATTG	10013
rs375159366	snp	A/G			intron-variant	HDAC6	GRCh38.p7	X:48805559	TCTGGGTGAAGGGCA[A/G]GGAGCTGACCTGACC	10013
rs375164434	snp	C/T	6.52614e-05	0.00571195	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823383	TGGCCCAGACCACCT[C/T]GGAGGCAGCCATGGA	10013
rs375225259	snp	C/T			intron-variant	HDAC6	GRCh38.p7	X:48815825	GGGTCACCTGAGTTC[C/T]AGAGTATGACGGGGA	10013
rs375315596	snp	A/G	0.000197592	0.00993765	intron-variant, utr-variant-3-prime	HDAC6	GRCh38.p7	X:48806596	CCTTTCTGGCTCCCC[A/G]CTGTCTCTCCAGAAC	10013
rs375317562	snp	C/T	0.000442596	0.0148695	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48824095	AGGAAGGGGATGGGG[C/T]GGAGGTTGGCCCGGG	10013
rs375340273	snp	C/T	2.31747e-05	0.00340394	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48822710	CTGCTGACCCTGCCA[C/T]GGCCCCCACTATCAG	10013
rs375393863	snp	A/G	0.000189982	0.00974449	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48808064	GCCCAGCACAGTCTT[A/G]TGGATGGCTATTGCA	10013
rs375526405	snp	C/T	0.000440973	0.0148422	intron-variant	HDAC6	GRCh38.p7	X:48805608	TAACCCTTTACCCCA[C/T]TTTATTCCTCATCTC	10013
rs375641404	snp	C/T			upstream-variant-2KB	HDAC6	GRCh38.p7	X:48801293	TAACTCGGAAAATCC[C/T]CACATTTAGCATCGT	10013
rs375703316	snp	A/G			upstream-variant-2KB	HDAC6	GRCh38.p7	X:48800613	GGTTCACGTAGGAGG[A/G]GTGAGAGGGAAGAGG	10013
rs375716236	snp	C/G	2.47439e-05	0.00351729	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48822971	AAGAAGGCACCCCAA[C/G]CAGCCAAACCTAGGT	10013
rs375722411	snp	A/C/G	0.000296145	0.0121655	synonymous-codon, missense, nc-transcript-variant, intron-variant	HDAC6	GRCh38.p7	X:48802743	GCAGCGAAGAAGTAG[A/C/G]CAGAACCCCCAGTCG	10013
rs376189568	snp	A/C	0.000216826	0.0104099	intron-variant	HDAC6	GRCh38.p7	X:48815361	GTCCTTTCCTGATCC[A/C]CCTTCACAACTCCTT	10013
rs376234935	snp	C/G	0.000283997	0.0119129	intron-variant, upstream-variant-2KB	HDAC6	GRCh38.p7	X:48802657	CGCTCCTCCCCCCAC[C/G]CCCAGAACCGCGGCA	10013
rs376270415	snp	A/G	2.90947e-05	0.00381399	intron-variant	HDAC6	GRCh38.p7	X:48823591	CAGCGAATCTCAGGT[A/G]AGGCTCACCACACCC	10013
rs376331158	snp	C/T			intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48815231	AGCATAATGTAATCA[C/T]CTCATATCATTGTCC	10013
rs376434799	snp	A/C	0.000189982	0.00974449	intron-variant	HDAC6	GRCh38.p7	X:48823620	CCAGGTAGGGGCAAG[A/C]AGGGGCAAGAATCGG	10013
rs376536218	snp	C/T	2.55047e-05	0.00357095	intron-variant	HDAC6	GRCh38.p7	X:48817322	GCACCCTGCTGCTTC[C/T]CAGGTTCTGAATGGT	10013
rs376760366	snp	C/T	5.06073e-05	0.00503002	intron-variant, utr-variant-3-prime	HDAC6	GRCh38.p7	X:48806573	TAGGGCTGTTCTCTC[C/T]CTTACTCCCTTTCTG	10013
rs376813905	snp	A/G	2.77627e-05	0.00372567	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48805464	GCCCTGAGCGGCTCC[A/G]TGCCATCAAGGAGCA	10013
rs376875887	snp	C/T	0.000169907	0.00921545	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48802953	GCAAAATGAAGAAGC[C/T]CGGCCAAGCAATGGA	10013
rs377099993	snp	A/G	0.000119983	0.0077445	intron-variant	HDAC6	GRCh38.p7	X:48816294	CGGTGCCTGGGGTGG[A/G]TGGATTCCCAGGACT	10013
rs377117130	snp	A/G	2.50916e-05	0.00354192	intron-variant	HDAC6	GRCh38.p7	X:48816652	TGTCCTCTGTGGGCT[A/G]GGGAGAGGAGGACCT	10013
rs377285286	snp	C/T	2.29368e-05	0.00338643	intron-variant	HDAC6	GRCh38.p7	X:48816124	TAAGCCTCTACCTCT[C/T]GTTTCCCCACTGCTA	10013
rs377345806	snp	C/T	2.29197e-05	0.00338517	synonymous-codon, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48824044	AACAATCCAAGAGAA[C/T]TGGGTGTGTCTCTCT	10013
rs377431255	snp	C/G			intron-variant	HDAC6	GRCh38.p7	X:48804891	TAAGTCATGGAGACA[C/G]TTGGAGGAAGAGTAT	10013
rs377440667	snp	A/G	5.44203e-05	0.00521605	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48823115	GCTGTGGTGGCCCTC[A/G]CTCAGGACCAGCCCT	10013
rs377532603	snp	C/T	4.88132e-05	0.00494006	intron-variant, utr-variant-3-prime	HDAC6	GRCh38.p7	X:48806605	CTCCCCACTGTCTCT[C/T]CAGAACTCATACTCC	10013
rs377535555	snp	A/G	4.67497e-05	0.00483453	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48824104	ATGGGGCGGAGGTTG[A/G]CCCGGGAGCAAACTG	10013
rs377538109	snp	A/G	0.000251656	0.0112145	missense, utr-variant-3-prime, nc-transcript-variant	HDAC6	GRCh38.p7	X:48806424	ATGAGGGAGAACTCC[A/G]TGTCCTAGCAGACAC	10013
rs377605184	snp	C/G	0.000726403	0.019044	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48814899	GGACCCCAAGGTAAG[C/G]CAGGCTCCCTGGGGC	10013
rs398122390	snp	A/T			utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	HDAC6, ERAS	GRCh38.p7	X:48824894	GAGGGAGCTGATATC[A/T]TGAGGATAACATTGG	10013
rs781782907	snp	A/G			intron-variant	HDAC6	GRCh38.p7	X:48803967	CAGGAGTTCGAGACC[A/G]GTCTGACCAACGCGA	10013
rs781785363	snp	C/G	0.00158814	0.0281345	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48815164	TACTAGCTGGACAAC[C/G]TTGCATAAGTCACTT	10013
rs781786871	snp	A/G	3.30175e-05	0.00406296	missense, intron-variant, nc-transcript-variant	HDAC6	GRCh38.p7	X:48818357	ACGGGCCCCGCATGG[A/G]TGATGCTGACTACCT	10013
rs781787249	snp	C/T	0.00211696	0.0324653	intron-variant	HDAC6	GRCh38.p7	X:48811530	TGTTTTCCTGAAAGG[C/T]ATTTCCCCAGAATGG	10013
rs781788475	snp	C/T	3.3953e-05	0.00412011	intron-variant	HDAC6	GRCh38.p7	X:48805427	CTGTGACTGTGACTC[C/T]ATCTCCCCAGCTTCC	10013
rs781789489	snp	C/T	2.31898e-05	0.00340505	missense, nc-transcript-variant, utr-variant-3-prime	HDAC6	GRCh38.p7	X:48822707	CCCCTGCTGACCCTG[C/T]CACGGCCCCCACTAT	10013
rs781792692	snp	A/G	5.7314e-05	0.00535292	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823423	ACTGGACCAGACTAC[A/G]TCAGAGGAGGCTCCA	10013
rs781792967	snp	G/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48814037	AGGGGCAGGTAGTGG[G/T]CGGACATGATCTAGA	10013
rs781793489	snp	A/G	9.61492e-05	0.00693292	intron-variant	HDAC6	GRCh38.p7	X:48818190	AGCCCCTAACCAGCC[A/G]TGGTCCGCTTCCCAC	10013
rs781794737	snp	A/G	5.01027e-05	0.00500488	synonymous-codon, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48822958	TAAGTTGGTCACCAA[A/G]AAGGCACCCCAACCA	10013
rs781795232	snp	C/G	0.000529661	0.016265	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48805513	CCTAGATCGCTGCGT[C/G]TCCTTTCAGGTAAGG	10013
rs781796142	snp	C/G	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48809891	GTAGTTTTATCTAGC[C/G]TTCTTCCTAGCTGAC	10013
rs781797483	snp	C/T			intron-variant	HDAC6	GRCh38.p7	X:48809570	AGTACTTTGGGAGGC[C/T]GAGGCGGATCACCTG	10013
rs781798715	snp	A/C	5.86743e-05	0.00541606	intron-variant	HDAC6	GRCh38.p7	X:48823598	TCTCAGGTAAGGCTC[A/C]CCACACCCAGGTAGG	10013
rs781800052	snp	C/T	0.00105904	0.0229869	intron-variant	HDAC6	GRCh38.p7	X:48811991	TATTTCAGAATGCAT[C/T]TCTAAAACATAAGTA	10013
rs781800091	snp	C/G			intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48820596	GATGGCACATTTACT[C/G]ATGGCAGAACCAGGA	10013
rs781801368	snp	G/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48818567	CCAGGGCAGTTGGTG[G/T]CTGTGATCACCTTGT	10013
rs781804134	snp	A/G	0.00105904	0.0229869	intron-variant	HDAC6	GRCh38.p7	X:48804094	CTTGATCTGGGAGGC[A/G]GAGGTTGCAGTGAGC	10013
rs781805615	snp	G/T	2.87906e-05	0.00379401	intron-variant	HDAC6	GRCh38.p7	X:48817476	TAAGGACTCCCTGGG[G/T]ACCCCCCAAATCCTG	10013
rs781805756	snp	A/G	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48807908	CATTACTCAGTTCCC[A/G]GCAGATTTTTAGGCA	10013
rs781806488	snp	G/T			intron-variant	HDAC6	GRCh38.p7	X:48816707	TCTGCTGTTTCTGGA[G/T]GCTCTGAGAGAGTCA	10013
rs781806990	snp	A/G	0.00105904	0.0229869	intron-variant, upstream-variant-2KB	HDAC6	GRCh38.p7	X:48801539	GGGGCGGCGGCTATG[A/G]CATCCGGGACGACAG	10013
rs781807565	snp	A/G	2.47464e-05	0.00351747	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48815934	AATGTAGAGGAGAGC[A/G]AGGAGGAAGGACCCT	10013
rs781810220	snp	C/T	3.30584e-05	0.00406548	intron-variant	HDAC6	GRCh38.p7	X:48808237	TCCTTGCACAGAGTC[C/T]CCTCTCTCTGCTGCT	10013
rs781810340	snp	C/T	2.42615e-05	0.00348284	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48816604	ACTGGCGCTGCCTGC[C/T]GCCTGGTGGAGGCTG	10013
rs781813174	snp	G/T	2.39639e-05	0.00346141	missense, utr-variant-3-prime, nc-transcript-variant	HDAC6	GRCh38.p7	X:48806624	AACTCATACTCCTGT[G/T]CCTGCCTGGCCTCAG	10013
rs781814032	snp	C/T	4.71365e-05	0.00485448	intron-variant	HDAC6	GRCh38.p7	X:48815554	CATTCCTTGACATCA[C/T]ATTTTCTCCCTGCCC	10013
rs781814159	snp	A/C			intron-variant	HDAC6	GRCh38.p7	X:48814154	TGTTTGCTGAGGGAG[A/C]GGTTCTGGTGAGAGA	10013
rs781814834	snp	C/T	2.61493e-05	0.00361579	intron-variant	HDAC6	GRCh38.p7	X:48803107	AATGGATCTGTGTCT[C/T]CTTTTTTTTTTCCTC	10013
rs781815084	snp	A/C	5.49609e-05	0.00524189	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48802979	ATGGAAGAAGACCTA[A/C]TCGTGGGACTGCAAG	10013
rs781816916	snp	G/T	3.18248e-05	0.00398891	intron-variant, utr-variant-3-prime	HDAC6	GRCh38.p7	X:48806742	ACTTTTTACATTGTT[G/T]TAAAGTCCTTCCTTC	10013
rs781817492	snp	A/G			intron-variant, upstream-variant-2KB	HDAC6	GRCh38.p7	X:48801625	GCGCCTGCCTTTTAC[A/G]TAGGCGCAGCACAGC	10013
rs781818835	snp	A/G	4.59908e-05	0.00479513	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48816008	GTCTCGCACAGGGCT[A/G]GTCTATGACCAAAAT	10013
rs781821341	snp	C/T	4.98405e-05	0.00499177	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48803136	TCTGCAGGATCTGAA[C/T]CTTGAGGCTGAAGCA	10013
rs781821510	snp	C/T			intron-variant	HDAC6	GRCh38.p7	X:48809019	TAGTACCTCTTAAAG[C/T]ATCTCGTTCTTTGTA	10013
rs781823204	snp	A/C	6.89077e-05	0.00586934	intron-variant	HDAC6	GRCh38.p7	X:48816096	GTGTTGGGGGTCCCT[A/C]CCCCTCAGGCACTAA	10013
rs781823349	snp	C/T	2.35139e-05	0.00342876	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48824289	CAGGCCTATGTCCAC[C/T]ACCAGGTGGGCCCTG	10013
rs781823789	snp	A/G	2.54336e-05	0.00356597	intron-variant, utr-variant-3-prime	HDAC6	GRCh38.p7	X:48806560	GCAGCTGAGTGGATA[A/G]GGCTGTTCTCTCCCT	10013
rs781824028	in-del	-/C	0.000486099	0.0155825	frameshift-variant, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823490	GCACAGACCACCAGA[-/C]CCCCCCCAACCTCAC	10013
rs781824701	snp	C/G	3.40472e-05	0.00412583	intron-variant	HDAC6	GRCh38.p7	X:48819972	TAGTCTCCAGGTTCT[C/G]TGTCTCCATCTCTCT	10013
rs781824833	snp	A/C	0.000529661	0.016265	intron-variant, upstream-variant-2KB	HDAC6	GRCh38.p7	X:48801618	ACCGCCGGCGCCTGC[A/C]TTTTACGTAGGCGCA	10013
rs781829631	snp	A/T	3.303e-05	0.00406373	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48822823	GGGGTGATGGGGGGA[A/T]CCCAGGGAAGGAGGG	10013
rs781831075	snp	A/G/T	2.43016e-05	0.00348572	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48816231	CCTCACCCTGACACC[A/G/T]CGCCCTGCCACAGAG	10013
rs781832503	snp	C/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48824505	AGGTAGAGGGGTCCT[C/T]ACTCTCTCTCACCTG	10013
rs781833780	snp	A/C/G	0.00032085	0.0126623	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823512	CAACCTCACCTGTGC[A/C/G]GGGAACTACACCCCA	10013
rs781833812	snp	A/C	0.00105904	0.0229869	intron-variant	HDAC6	GRCh38.p7	X:48811140	GAAACCCCATCTCTA[A/C]TAAAAATACAAAAAT	10013
rs781835040	snp	A/C	0.00153938	0.0277006	synonymous-codon, nc-transcript-variant, utr-variant-3-prime	HDAC6	GRCh38.p7	X:48822691	CCTTGGAGACCCACC[A/C]CCCCTGCTGACCCTG	10013
rs781835436	snp	C/G	0.000529661	0.016265	upstream-variant-2KB	HDAC6	GRCh38.p7	X:48800618	ACGTAGGAGGGGTGA[C/G]AGGGAAGAGGCGGCA	10013
rs781835578	snp	A/G	3.00784e-05	0.00387792	missense, intron-variant, nc-transcript-variant	HDAC6	GRCh38.p7	X:48818351	CATGGAACGGGCCCC[A/G]CATGGGTGATGCTGA	10013
rs781836327	snp	A/G	0.000101562	0.00712534	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48814717	GCTGCTTTCCTGCAC[A/G]TCCTGCTGCCAGTCG	10013
rs781837169	snp	A/G	0.000149653	0.00864894	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823328	GGGGGAGCCACGCTG[A/G]GCCAGACTACCTCAG	10013
rs781837182	snp	A/T	2.63262e-05	0.003628	intron-variant	HDAC6	GRCh38.p7	X:48816674	GGAGGACCTGGGGGG[A/T]ATGGAAAAAGAGAGC	10013
rs781838587	snp	C/T			intron-variant	HDAC6	GRCh38.p7	X:48804504	TCTTATTTTCCTAGC[C/T]CATGACATTGTTTGC	10013
rs781841990	snp	C/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48819899	CTATTTCTTCTACCT[C/T]TGAGTCTGTATTTCT	10013
rs781845599	snp	A/G	3.38129e-05	0.00411161	intron-variant	HDAC6	GRCh38.p7	X:48818132	CTGCAGTCAGGGGCC[A/G]CAGTGTGATCAGGGA	10013
rs781847242	snp	C/G	2.61387e-05	0.00361506	intron-variant	HDAC6	GRCh38.p7	X:48814627	CCCTTCTGTCAGCGG[C/G]TCGGGACAGGTGGCT	10013
rs781847976	snp	C/T			intron-variant	HDAC6	GRCh38.p7	X:48811854	TTCTGGCTTCTGGAA[C/T]TTAATGCTTCAACAT	10013
rs781848137	snp	C/T	4.24935e-05	0.00460922	intron-variant	HDAC6	GRCh38.p7	X:48816300	CTGGGGTGGGTGGAT[C/T]CCCAGGACTGTGGAT	10013
rs781850986	snp	A/C	0.000529661	0.016265	upstream-variant-2KB	HDAC6	GRCh38.p7	X:48800707	CAGTCTGATGCAGAA[A/C]CCCCGGACTGCTTAT	10013
rs781851100	snp	C/T	7.66401e-05	0.00618984	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48815068	TGAGTGACTCACCTT[C/T]GTCCCTCAGCCTGTG	10013
rs781852716	snp	A/C	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48804011	CTACTAAAAATACAA[A/C]AATTAGTTGGGCGTG	10013
rs781853093	snp	C/G	2.37722e-05	0.00344754	missense, nc-transcript-variant, intron-variant	HDAC6	GRCh38.p7	X:48817371	CCAGGACACCACGCA[C/G]AGCAGGATGCAGCTT	10013
rs781853300	snp	A/G			intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48807083	GGCATGTAAAATCAT[A/G]GTACATCTTATCATC	10013
rs781854201	snp	A/C	0.000141243	0.00840247	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48824133	TGCAGGGGGATGCTG[A/C]CCCCCACCTGACACT	10013
rs781857215	snp	C/G	8.08702e-05	0.00635834	intron-variant, utr-variant-3-prime, nc-transcript-variant	HDAC6	GRCh38.p7	X:48805686	GGTGAAGGCTTGGGA[C/G]CCTTGTAGGGATGGG	10013
rs781858100	snp	C/T	3.35076e-05	0.004093	intron-variant	HDAC6	GRCh38.p7	X:48808374	CCCAGCCACCTCCCA[C/T]CCTTACAGGCCCAGC	10013
rs781858496	snp	A/G	2.56456e-05	0.0035808	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48815912	GAGGGACAACATGGA[A/G]GAGGACAATGTAGAG	10013
rs781858924	snp	A/G	2.36827e-05	0.00344104	intron-variant, nc-transcript-variant	HDAC6	GRCh38.p7	X:48814799	AGGTTAGGCTGTGAG[A/G]GTAGGTAGCCTCATG	10013
rs781859538	snp	C/T	5.25183e-05	0.0051241	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823778	GATCTAGGGGCCTCA[C/T]TGATCAGGTGAGCTC	10013
rs781860199	snp	A/C	2.47881e-05	0.00352043	missense, upstream-variant-2KB, nc-transcript-variant	HDAC6, ERAS	GRCh38.p7	X:48824603	GGAGGATATGCCCCA[A/C]CCACACTAAGCCCCA	10013
rs781860471	snp	C/T			intron-variant	HDAC6	GRCh38.p7	X:48804093	GCTTGATCTGGGAGG[C/T]GGAGGTTGCAGTGAG	10013
rs781862589	snp	G/T	3.76634e-05	0.00433939	intron-variant	HDAC6	GRCh38.p7	X:48808180	GGGTGGCATGGGGTG[G/T]GGTGTCCTGGTCTGG	10013
rs781864550	snp	A/G	3.29794e-05	0.00406061	missense, nc-transcript-variant, intron-variant	HDAC6	GRCh38.p7	X:48802739	CCAGGCAGCGAAGAA[A/G]TAGGCAGAACCCCCA	10013
rs781864680	in-del	-/T	0.0217041	0.101887	intron-variant	HDAC6	GRCh38.p7	X:48803109	TGGATCTGTGTCTCC[-/T]TTTTTTTTTCCTCTG	10013
rs781864773	snp	C/T	2.32842e-05	0.00341198	synonymous-codon, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48824270	AGCCTGGTGTTACTA[C/T]TGTCAGGCCTATGTC	10013
rs781864802	snp	C/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48810220	AGCTAGGACTGCAGG[C/T]ATGTGCCACCACACC	10013
rs781865210	snp	C/G/T	0.00017934	0.00946789	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48805443	ATCTCCCCAGCTTCC[C/G/T]GGAAGGCCCTGAGCG	10013
rs781865218	snp	C/G	3.11745e-05	0.00394795	intron-variant	HDAC6	GRCh38.p7	X:48823623	GGTAGGGGCAAGAAG[C/G]GGCAAGAATCGGGCT	10013
rs781865878	snp	C/T	4.86304e-05	0.00493081	synonymous-codon, nc-transcript-variant, intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48820228	GCTGATGGGCCTTGC[C/T]AGTGGCCGCATTATC	10013
rs781867791	snp	C/G	3.20302e-05	0.00400176	synonymous-codon, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48823162	GGGAGCCACTCTGGC[C/G]CAGACCATTTCTGAG	10013
rs781868990	snp	C/T	3.01996e-05	0.00388573	intron-variant, utr-variant-3-prime	HDAC6	GRCh38.p7	X:48806730	CTACAGCATTTGACT[C/T]TTTACATTGTTTTAA	10013
rs781871653	snp	C/T	0.000153504	0.00875947	intron-variant	HDAC6	GRCh38.p7	X:48819947	TTTCAGTCTCTGCTT[C/T]TGTGTCTCCTAGTCT	10013
rs781872521	snp	C/T	5.89432e-05	0.00542845	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48815399	GGTGGCTACAACCTC[C/T]GCGCCCTGGCTGAAG	10013
rs781873093	snp	A/C	3.43147e-05	0.004142	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48808129	TCAACAGAAACACCG[A/C]ATCCGGAGGTCAGCA	10013
rs781873237	snp	C/T	2.67041e-05	0.00365394	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823503	AGACCCCCCCAACCT[C/T]ACCTGTGCAGGGAAC	10013
rs781873841	snp	C/T	8.74929e-05	0.00661353	intron-variant	HDAC6	GRCh38.p7	X:48817995	AGCCCAGCCCTCTTC[C/T]AGGGCGTGAGTATCG	10013
rs781874285	snp	A/G	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48821135	GAGCCACCGCACCTG[A/G]CCCCTGGTTACTGTT	10013
rs781875709	snp	A/G	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48814282	TGGAAGAATGGATTC[A/G]TGGATTAAATAATTA	10013
rs781875722	snp	C/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48822334	TGAAGTACTTAAAAT[C/T]GGGTCTGGCACACAG	10013
rs781875759	snp	A/G			intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48807344	TTGCTGTTTTAAAAA[A/G]ATGCTACAGCAAATA	10013
rs781877739	snp	C/T	2.32764e-05	0.0034114	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48815989	TGACATGGCCAGTGC[C/T]ACAGTCTCGCACAGG	10013
rs781879219	snp	A/C	4.87413e-05	0.00493642	synonymous-codon, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48822983	CAACCAGCCAAACCT[A/C]GGTTAGCTGAGCGGA	10013
rs781881555	snp	C/T	3.2981e-05	0.00406071	synonymous-codon, intron-variant, nc-transcript-variant	HDAC6	GRCh38.p7	X:48818343	CAACGTGGCATGGAA[C/T]GGGCCCCGCATGGGT	10013
rs781881588	in-del	-/G	0.000112765	0.00750798	intron-variant, upstream-variant-2KB	HDAC6	GRCh38.p7	X:48802642	CCCTCACATACCCAC[-/G]GCTCCTCCCCCCACC	10013
rs781884966	snp	A/G	2.55157e-05	0.00357172	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48822816	GGATTTGGGGGTGAT[A/G]GGGGGAACCCAGGGA	10013
rs781886808	snp	C/T	0.00158814	0.0281345	intron-variant	HDAC6	GRCh38.p7	X:48821417	AGGCTGGTGTTGAAC[C/T]CCTGACCTCGTGATC	10013
rs781888244	snp	A/C/G	0.00264606	0.0362887	intron-variant	HDAC6	GRCh38.p7	X:48812994	CTCACTGCAACCTCC[A/C/G]CCTCCTGGGTTCAAG	10013
rs781889204	snp	A/T	3.8768e-05	0.00440255	intron-variant	HDAC6	GRCh38.p7	X:48816291	CCCCGGTGCCTGGGG[A/T]GGGTGGATTCCCAGG	10013
rs781892024	snp	C/T			intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48820428	CCTTAATTGAGTGCT[C/T]ACTATGTGCAGAGCA	10013
rs781892999	snp	A/G			intron-variant	HDAC6	GRCh38.p7	X:48812199	ATTACACACACAGAT[A/G]TGAAACACTGTGAAT	10013
rs781893810	snp	G/T	4.76383e-05	0.00488026	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48808036	TGTCTTGCCCAGGCC[G/T]CCTGGACATCACGCC	10013
rs781894057	snp	C/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48811464	ACCCAAGAATGAAGG[C/T]CCATTGTAGGGGGCT	10013
rs781894555	snp	C/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48817612	TACCCAGAGAAGGAC[C/T]GAGGATGGAGCCTCT	10013
rs781897644	snp	A/C/T	4.82303e-05	0.00491052	intron-variant	HDAC6	GRCh38.p7	X:48814614	AGGCCCAGCCCCGCC[A/C/T]TTCTGTCAGCGGCTC	10013
rs781898016	snp	A/C	2.52557e-05	0.00355348	intron-variant, utr-variant-3-prime	HDAC6	GRCh38.p7	X:48806577	GCTGTTCTCTCCCTT[A/C]CTCCCTTTCTGGCTC	10013
rs781899448	snp	A/G	2.58331e-05	0.00359387	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48803181	CTTGGTGTTGGATGA[A/G]CAGTTAAATGAATTC	10013
rs781901449	snp	C/T			intron-variant, upstream-variant-2KB	HDAC6	GRCh38.p7	X:48801534	ACGGAGGGGCGGCGG[C/T]TATGGCATCCGGGAC	10013
rs781902196	snp	C/G	2.66216e-05	0.0036483	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823753	ATGGCTGATTCGATG[C/G]TGATGCAGGGATCTA	10013
rs781903016	snp	G/T	2.70307e-05	0.00367622	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823528	GGGAACTACACCCCA[G/T]ATATCTCCCAGTACA	10013
rs781904146	snp	C/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48819744	GAGACAGGGTTTCAC[C/T]GTGTTAGCCAGGATG	10013
rs781905937	snp	C/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48809756	GCAGTGAGCTGAGAT[C/T]GCACCACTGCACTCC	10013
rs781906565	snp	A/G	0.000114651	0.0075705	intron-variant	HDAC6	GRCh38.p7	X:48816125	AAGCCTCTACCTCTC[A/G]TTTCCCCACTGCTAG	10013
rs781907553	snp	A/C	3.03601e-05	0.00389604	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48802909	CGTTCCCCGCTCTAT[A/C]CCCAATCTAGCGGAG	10013
rs781907567	snp	A/C	3.32347e-05	0.00407631	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823378	TACACTGGCCCAGAC[A/C]ACCTCGGAGGCAGCC	10013
rs781908358	snp	A/C	3.34258e-05	0.00408801	intron-variant	HDAC6	GRCh38.p7	X:48808364	GTGCTAGACTCCCAG[A/C]CACCTCCCACCCTTA	10013
rs781908694	snp	A/G	5.38018e-05	0.00518633	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48822875	GGCAGGAAGGGTGAC[A/G]GTACCCACACTCAAG	10013
rs781909315	snp	C/T	3.97401e-05	0.00445741	intron-variant	HDAC6	GRCh38.p7	X:48805405	GCTCCCCAGTGTCCT[C/T]ATGCATCTGTGACTG	10013
rs781909716	snp	C/T	0.000529661	0.016265	intron-variant, upstream-variant-2KB	HDAC6	GRCh38.p7	X:48801708	TCAGCCCAGCTGGCG[C/T]AGCACGCCGACGCAC	10013
rs781911149	snp	C/T	7.13051e-05	0.00597055	intron-variant	HDAC6	GRCh38.p7	X:48808153	GTCAGCAACAGAGGG[C/T]AGATGTGATGGGGGT	10013
rs781914401	snp	C/T	0.000529661	0.016265	upstream-variant-2KB	HDAC6	GRCh38.p7	X:48801172	AATACTTGCTATCAT[C/T]ACCATTCCCTGCCCC	10013
rs781914689	snp	A/G	7.52181e-05	0.00613216	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48814732	GTCCTGCTGCCAGTC[A/G]CCCTCGAGGTCCTGG	10013
rs781915727	snp	C/T	0.00105904	0.0229869	intron-variant	HDAC6	GRCh38.p7	X:48822224	TGTGAGGCCAGGGGT[C/T]CCTGGACAGTGTGAA	10013
rs781916251	snp	A/G	6.09775e-05	0.00552132	missense, intron-variant, nc-transcript-variant	HDAC6	GRCh38.p7	X:48818275	TTCTTCCCCATGGGG[A/G]ATGAGGGTGCCAGCA	10013
rs781916616	snp	A/G			intron-variant	HDAC6	GRCh38.p7	X:48819135	CTGTATGTGCAAATA[A/G]CCAGCTCTTGTGGAC	10013
rs781918298	snp	A/G	2.37849e-05	0.00344846	missense, utr-variant-3-prime, nc-transcript-variant	HDAC6	GRCh38.p7	X:48806663	CTCAGGCTGGTGGAT[A/G]CGGTCCTGGGGGCTG	10013
rs781918532	snp	C/T	5.41338e-05	0.0052023	intron-variant	HDAC6	GRCh38.p7	X:48815517	TGGAGGAGGGGAAAG[C/T]GGGAGCCTCACTGCC	10013
rs781919186	snp	A/G	8.45059e-05	0.00649968	intron-variant	HDAC6	GRCh38.p7	X:48808347	CCCCGACTCCCACCT[A/G]GGTGCTAGACTCCCA	10013
rs781919553	snp	C/G			intron-variant	HDAC6	GRCh38.p7	X:48811282	GCACTCCAGCCTGGG[C/G]GATAGAGGGAGACCC	10013
rs781920475	snp	A/G	4.15024e-05	0.00455516	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48815325	ATTATCATCATTATT[A/G]TTATTCCCTGGTCAT	10013
rs781921555	snp	C/T	0.000529661	0.016265	upstream-variant-2KB	HDAC6	GRCh38.p7	X:48799966	AGGAACAGGAACCCA[C/T]AGTCTGGAGCTCTCT	10013
rs781923733	snp	C/T			upstream-variant-2KB	HDAC6	GRCh38.p7	X:48801327	CACGCCTATTTTGGC[C/T]GCCACCACCAACGTC	10013
rs781924490	snp	A/G	5.30434e-05	0.00514965	intron-variant	HDAC6	GRCh38.p7	X:48803085	TTCCCTCTGACTCAG[A/G]GCCTAAAATGGATCT	10013
rs781929744	snp	A/G	2.52516e-05	0.00355319	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48822810	GTGAGTGGATTTGGG[A/G]GTGATGGGGGGAACC	10013
rs781932009	snp	A/G			downstream-variant-500B, upstream-variant-2KB	HDAC6, ERAS	GRCh38.p7	X:48825150	CTTGACTGGCTCCAC[A/G]GGATATAAAATGGTA	10013
rs781932316	in-del	-/G	0.00158814	0.0281345	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48822816	GGATTTGGGGGTGAT[-/G]GGGGGAACCCAGGGA	10013
rs781932506	snp	A/G	2.28266e-05	0.00337828	synonymous-codon, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48823972	TCCCCATTTGGTGGC[A/G]GTATGCCCCATACCT	10013
rs781933748	snp	A/G	0.000133477	0.00816829	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823499	CACCAGACCCCCCCA[A/G]CCTCACCTGTGCAGG	10013
rs781934879	snp	C/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48812451	GATTCAGTGAGTTGG[C/T]TCTTCAGAAGGGATT	10013
rs781935289	snp	A/T	2.46697e-05	0.00351202	intron-variant	HDAC6	GRCh38.p7	X:48822614	CTCCCCTTTTCCTTA[A/T]CAAAGGGTGGCTATA	10013
rs781936382	snp	A/G	9.68617e-05	0.00695855	intron-variant	HDAC6	GRCh38.p7	X:48802842	AGTTGGTCATGCCCT[A/G]GACTCTGACCCTTCT	10013
rs781937068	snp	A/G	3.30098e-05	0.00406249	intron-variant	HDAC6	GRCh38.p7	X:48805566	GAAGGGCAGGGAGCT[A/G]ACCTGACCTGGGTGC	10013
rs781937590	snp	C/T	1.64789e-05	0.0028704	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48816240	GACACCGCGCCCTGC[C/T]ACAGAGGCTGAGCTG	10013
rs781941748	snp	A/G	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48820968	TCAGCCTCCTGAGTC[A/G]CTGGGATTACAGGCA	10013
rs781942141	snp	C/G	0.00211696	0.0324653	intron-variant	HDAC6	GRCh38.p7	X:48810876	TTTGCTGTGACCTGG[C/G]AGATTTTGTCAACTT	10013
rs781942946	snp	G/T	0.000318624	0.0126179	intron-variant, upstream-variant-2KB, utr-variant-5-prime	HDAC6	GRCh38.p7	X:48801964	GTACAGCGCGTCGAC[G/T]GCGGAGGCGGGAAGG	10013
rs781944555	snp	C/T	2.40402e-05	0.00346692	intron-variant	HDAC6	GRCh38.p7	X:48820054	CCATCACTTACTGCC[C/T]ACCAAAAGCCCCTAC	10013
rs781946147	snp	A/G	3.29652e-05	0.00405974	missense, intron-variant, nc-transcript-variant	HDAC6	GRCh38.p7	X:48818326	GGCACAGGCTTCACC[A/G]TCAACGTGGCATGGA	10013
rs781948392	snp	C/T	2.29674e-05	0.00338868	intron-variant	HDAC6	GRCh38.p7	X:48816094	AGGTGTTGGGGGTCC[C/T]TCCCCCTCAGGCACT	10013
rs781950553	snp	C/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48821799	AGGGGTGAGCCACCG[C/T]GCCCAGCCTGTGCTG	10013
rs781953295	snp	C/T	6.89275e-05	0.00587018	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48815389	CTTGCCCCAGGGTGG[C/T]TACAACCTCCGCGCC	10013
rs781955550	snp	A/G	3.21926e-05	0.00401189	intron-variant	HDAC6	GRCh38.p7	X:48815844	GTATGACGGGGATTC[A/G]GATTGAGAGGGTAGG	10013
rs781955760	snp	G/T	2.50084e-05	0.00353604	synonymous-codon, nc-transcript-variant, intron-variant	HDAC6	GRCh38.p7	X:48817328	TGCTGCTTCCCAGGT[G/T]CTGAATGGTGCTGCT	10013
rs781956368	snp	A/G			downstream-variant-500B, upstream-variant-2KB	HDAC6, ERAS	GRCh38.p7	X:48825034	CATCCCTGGCCAGCA[A/G]AGCCGATGAGTAATG	10013
rs781958232	in-del	-/GGA	4.89039e-05	0.00494465	intron-variant, nc-transcript-variant	HDAC6	GRCh38.p7	X:48814764	ATCTGGGGTGTGTTG[-/GGA]GGAGGAGGAGTGGCC	10013
rs781959020	snp	C/T			intron-variant	HDAC6	GRCh38.p7	X:48813942	AGCCTTAGCTGGCTC[C/T]CCGCAGCTAAGAGCC	10013
rs781964171	snp	A/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48813739	CCTATAAAATAGAAG[A/T]AGTAGTAGAGGTGGC	10013
rs781964685	snp	A/C	5.56746e-05	0.00527581	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48805498	GATCCAGGAGGGCCT[A/C]CTAGATCGCTGCGTG	10013
rs781964788	snp	A/G	0.000182066	0.0095394	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48805647	CCCGGTTTGCTGAAA[A/G]GGAAGAGCTGATGTT	10013
rs781965120	in-del	-/A	0.0026455	0.0362733	intron-variant	HDAC6	GRCh38.p7	X:48817096	TACTAAAAAACATAC[-/A]AAAAAATTAGCCGGG	10013
rs781969397	snp	C/T	5.7076e-05	0.00534179	intron-variant	HDAC6	GRCh38.p7	X:48815499	GCCGGAGGTGAGCCC[C/T]GGTGGAGGAGGGGAA	10013
rs781969923	snp	A/C/G	7.12891e-05	0.00596995	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	HDAC6	GRCh38.p7	X:48806635	CTGTGCCTGCCTGGC[A/C/G]TCAGGCTCTGTCCTC	10013
rs781971013	snp	C/T	0.000529661	0.016265	intron-variant, upstream-variant-2KB	HDAC6	GRCh38.p7	X:48802611	CAGAGAGGTGGGGTC[C/T]TCAGGGCACACTAGC	10013
rs781971304	snp	C/T	0.00105904	0.0229869	intron-variant	HDAC6	GRCh38.p7	X:48811846	TTGTTCATTTCTGGC[C/T]TCTGGAATTTAATGC	10013
rs781973799	snp	A/G	3.29837e-05	0.00406088	intron-variant	HDAC6	GRCh38.p7	X:48805414	TGTCCTCATGCATCT[A/G]TGACTGTGACTCCAT	10013
rs781974405	snp	C/T	2.29729e-05	0.00338909	intron-variant	HDAC6	GRCh38.p7	X:48820095	ATACATCTCTTCTCT[C/T]CCTGCCTCAGTTTAA	10013
rs781974625	snp	A/G	1.64776e-05	0.00287028	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823580	TTGGAGCTAGGCAGC[A/G]AATCTCAGGTAAGGC	10013
rs781976763	snp	C/T	0.000529661	0.016265	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48807296	ATGTTAATCAGTCCC[C/T]GACTAATGGGCATTT	10013
rs781978059	snp	C/T	2.2883e-05	0.00338245	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48823949	GCTGTGACACCACTG[C/T]CCTGGTGTCCCCATT	10013
rs781979770	snp	C/T	2.28592e-05	0.00338069	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48814514	CCTCTAACTGGTCCA[C/T]CACAGGTTTCGGCCA	10013
rs781980272	snp	G/T	0.00317376	0.039709	intron-variant	HDAC6	GRCh38.p7	X:48817125	GGCGTGGCAGCAAGC[G/T]CCTGTAGTCCTAGCT	10013
rs781983675	snp	C/T	5.0067e-05	0.0050031	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48822805	CATGAGTGAGTGGAT[C/T]TGGGGGTGATGGGGG	10013
rs781984036	snp	A/G	0.00105904	0.0229869	intron-variant	HDAC6	GRCh38.p7	X:48807658	GCTGGGACTACAGTC[A/G]CCCGCCACCACACCC	10013
rs781984478	snp	C/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48813968	GAGCCCCATGCTCCA[C/T]TTGGGCCTCCAGTGT	10013
rs781985932	snp	C/T	2.52411e-05	0.00355245	intron-variant	HDAC6	GRCh38.p7	X:48822581	AAATTCCCCAATGAA[C/T]CCCCACCATACCTTT	10013
rs781989557	snp	A/G	0.00422943	0.0457911	intron-variant	HDAC6	GRCh38.p7	X:48810658	CTGTTGCCCAGACTG[A/G]AGTACAGTGGCACAA	10013
rs781991034	snp	C/T	2.46248e-05	0.00350882	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48816576	CAGTACCTTCGCCTG[C/T]GCACAGCTTGCCACT	10013
rs781993024	snp	A/G	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48808521	ACTGTTGGGTTCCCT[A/G]TTTTACAGATAGGGG	10013
rs781993404	snp	G/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48820828	TGGATCTGGTTTTTT[G/T]TTGTTGTTGTTGTTG	10013
rs781995480	snp	A/C	0.0026455	0.0362733	intron-variant	HDAC6	GRCh38.p7	X:48815817	TTCTGTTTGGGTCAC[A/C]TGAGTTCCAGAGTAT	10013
rs781996305	snp	A/C	2.39765e-05	0.00346232	intron-variant	HDAC6	GRCh38.p7	X:48814602	GCCCCCAAAGTGAGG[A/C]CCAGCCCCGCCCTTC	10013
rs781996775	snp	C/T			intron-variant	HDAC6	GRCh38.p7	X:48822242	TGGACAGTGTGAAGA[C/T]GGATTTCTGTATGGC	10013
rs781997603	in-del	-/GCC	0.00105904	0.0229869	upstream-variant-2KB	HDAC6	GRCh38.p7	X:48801324	ACCACGCCTATTTTG[-/GCC]GCCGCCACCACCAAC	10013
rs781998158	snp	A/C	2.39788e-05	0.00346249	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48816226	CGCTGCCTCACCCTG[A/C]CACCGCGCCCTGCCA	10013
rs781998776	snp	A/G			intron-variant	HDAC6	GRCh38.p7	X:48803949	AGGTGGATCACTTGA[A/G]GTCAGGAGTTCGAGA	10013
rs781999157	snp	C/T			intron-variant	HDAC6	GRCh38.p7	X:48811045	GCGGTGGCTCATGCC[C/T]GTAATCCCAGCACTT	10013
rs782001291	in-del	-/A	0.00104058	0.0227861	splice-acceptor-variant	HDAC6	GRCh38.p7	X:48814437	TTTTCTTCTGCCCCC[-/A]AGTGTCCTCTATTTC	10013
rs782002954	snp	C/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48803581	TCCTAAACTAGTATC[C/T]GGGCTTCCCAGAAGC	10013
rs782003620	snp	A/G	2.29447e-05	0.00338701	intron-variant	HDAC6	GRCh38.p7	X:48816077	TGGAGGGCTGGATGA[A/G]TAGGTGTTGGGGGTC	10013
rs782003936	snp	A/G			intron-variant	HDAC6	GRCh38.p7	X:48818713	GGCTGGATCTGTGTT[A/G]TATGTGCGTGCCATC	10013
rs782007750	snp	C/G	2.36784e-05	0.00344074	intron-variant, utr-variant-3-prime	HDAC6	GRCh38.p7	X:48806499	GGGCAGGGAATGGTG[C/G]CAATCTTGGGGTCCC	10013
rs782011369	snp	A/G			upstream-variant-2KB	HDAC6	GRCh38.p7	X:48801113	CAGCCTTAATAATGG[A/G]AACTACCTCATAGAA	10013
rs782011997	snp	C/G			intron-variant, utr-variant-3-prime, downstream-variant-500B	HDAC6	GRCh38.p7	X:48805871	GTTTGATGTGTGTCA[C/G]GTGCTTAGAACAGGG	10013
rs782012145	snp	C/T	2.77189e-05	0.00372272	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823712	GAGAGGAGAACCTAC[C/T]AGGAGAGGCAGCTGG	10013
rs782014624	snp	C/G	0.00105904	0.0229869	intron-variant	HDAC6	GRCh38.p7	X:48804931	GGGTGGGGGGGCCAG[C/G]TAGAGTAAAGTTCTA	10013
rs782014655	snp	C/T	0.00158814	0.0281345	intron-variant	HDAC6	GRCh38.p7	X:48821104	TAGCCTCCCAGAGTG[C/T]TGGAATTACAGGCAT	10013
rs782014772	snp	A/G	6.59315e-05	0.0057412	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48808107	TGGCTGTGGCAGCCC[A/G]CTATGCTCAACAGAA	10013
rs782015285	snp	A/G			intron-variant	HDAC6	GRCh38.p7	X:48813437	CACAACTACATTATC[A/G]ACCCATTAAAATGTG	10013
rs782017697	snp	A/C/T	3.77936e-05	0.00434688	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823323	CTGTTGGGGGAGCCA[A/C/T]GCTGGGCCAGACTAC	10013
rs782023371	snp	A/G			upstream-variant-2KB	HDAC6	GRCh38.p7	X:48800837	TGGAGTGGGAGTTGC[A/G]GGGGAGAGGGGGTGC	10013
rs782023778	snp	A/G	0.00035921	0.0133969	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823554	GTACACTGATTGGGA[A/G]TCTCAGGACCTTGGA	10013
rs782023893	snp	A/G	0.000111688	0.00747206	synonymous-codon, nc-transcript-variant, utr-variant-3-prime	HDAC6	GRCh38.p7	X:48818086	CGGTAATGGAACTCA[A/G]CACATGTTTGAGGAT	10013
rs782024086	in-del	-/A	0.000529661	0.016265	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48807180	GTAGTAACATGACAT[-/A]ACTCCCTTCGTACCA	10013
rs782024099	snp	C/G/T	5.18011e-05	0.00508904	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48823098	AGACTAACTCAGAGA[C/G/T]AGCTGTGGTGGCCCT	10013
rs782024221	snp	A/G			intron-variant	HDAC6	GRCh38.p7	X:48819808	GCCTCCCAAAGTGCT[A/G]GGATTACAGGCCTGA	10013
rs782025669	snp	C/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48803646	AAGGATGAAACCTCC[C/T]GTTTGCTTTACTTTT	10013
rs782025726	snp	C/T	9.38108e-05	0.00684811	synonymous-codon, nc-transcript-variant, utr-variant-3-prime	HDAC6	GRCh38.p7	X:48822664	GTCCATGGCTGCCTG[C/T]ACTCGCTCCCTCCTT	10013
rs782031274	snp	A/G	0.00211696	0.0324653	intron-variant	HDAC6	GRCh38.p7	X:48821930	GACACGGTGGGAGTT[A/G]AGAACACAGATGACT	10013
rs782033950	snp	C/G	2.5737e-05	0.00358718	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48822932	GAAGACAGAGAAGGA[C/G]CCTCCAGTTCTAAGT	10013
rs782035991	snp	C/T	2.29568e-05	0.0033879	intron-variant	HDAC6	GRCh38.p7	X:48816099	TTGGGGGTCCCTCCC[C/T]CTCAGGCACTAAGCC	10013
rs782036567	snp	A/G	6.63031e-05	0.00575736	intron-variant	HDAC6	GRCh38.p7	X:48818439	GATAGATCGCAGGAC[A/G]TATGTGACACGCCTG	10013
rs782036783	snp	A/G	0.000121269	0.00778587	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48816521	AAACCCGGGAGCTGC[A/G]CCGTGAGAGTTCCAA	10013
rs782037409	snp	C/G	3.8937e-05	0.00441214	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48815019	CACCTGCTCATGGGT[C/G]TGGCAGGAGGCAAGC	10013
rs782041149	snp	C/T	9.80657e-05	0.00700166	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48822785	TACTGGCGCAGCTTA[C/T]GGGTCATGAGTGAGT	10013
rs782041678	snp	A/G	3.7652e-05	0.00433873	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823307	ACCACCTCAGAGGAT[A/G]CTGTTGGGGGAGCCA	10013
rs782044479	snp	C/G	2.90761e-05	0.00381277	intron-variant	HDAC6	GRCh38.p7	X:48815875	ACAAACGTGGCCTCC[C/G]CCTTTTAGCTGAGAC	10013
rs782045023	snp	C/G	0.000529661	0.016265	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48815958	GGACCCTGGGAGCCC[C/G]CTGTGCTCCCAATCC	10013
rs782046921	snp	A/T	3.21973e-05	0.00401218	intron-variant	HDAC6	GRCh38.p7	X:48802844	TTGGTCATGCCCTGG[A/T]CTCTGACCCTTCTCT	10013
rs782048778	snp	C/G	2.2837e-05	0.00337905	intron-variant	HDAC6	GRCh38.p7	X:48819921	TGTATTTCTTTTCTT[C/G]CCTTCTTCATTTTCA	10013
rs782048817	in-del	-/G	2.66869e-05	0.00365277	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48822890	AGTACCCACACTCAA[-/G]GATCTCCCTCCCTGG	10013
rs782049075	snp	A/G	0.000252468	0.0112326	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48822811	TGAGTGGATTTGGGG[A/G]TGATGGGGGGAACCC	10013
rs782049351	snp	A/G	2.28238e-05	0.00337807	synonymous-codon, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48823975	CCATTTGGTGGCAGT[A/G]TGCCCCATACCTGCA	10013
rs782052369	snp	A/G	3.19739e-05	0.00399824	missense, intron-variant, nc-transcript-variant	HDAC6	GRCh38.p7	X:48818335	TTCACCGTCAACGTG[A/G]CATGGAACGGGCCCC	10013
rs782052389	snp	C/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48811031	AGTGCCGGCTGGGTG[C/T]GGTGGCTCATGCCTG	10013
rs782053378	snp	A/G	3.53033e-05	0.00420124	intron-variant	HDAC6	GRCh38.p7	X:48816281	ACAGGTCAGACCCCG[A/G]TGCCTGGGGTGGGTG	10013
rs782054361	snp	C/T	2.33689e-05	0.00341817	intron-variant	HDAC6	GRCh38.p7	X:48815560	TTGACATCATATTTT[C/T]TCCCTGCCCTGCAGT	10013
rs782057421	snp	C/T	2.41759e-05	0.00347669	synonymous-codon, nc-transcript-variant, utr-variant-3-prime	HDAC6	GRCh38.p7	X:48822632	AAGGGTGGCTATAAC[C/T]TGACATCCATCTCAG	10013
rs782057778	snp	C/T	2.29318e-05	0.00338606	intron-variant	HDAC6	GRCh38.p7	X:48820103	CTTCTCTCCCTGCCT[C/T]AGTTTAACCCAGAAC	10013
rs782060011	snp	A/C	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48819323	GCAGTACGTGTGGCT[A/C]TGTGTGACCATCTTC	10013
rs782060090	snp	A/G			intron-variant	HDAC6	GRCh38.p7	X:48811284	ACTCCAGCCTGGGCG[A/G]TAGAGGGAGACCCTG	10013
rs782060510	snp	C/T	0.000119965	0.00774391	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48818056	GATCCTGATTGTGGA[C/T]TGGGATGTCCACCAC	10013
rs782062686	snp	A/G	4.27625e-05	0.00462379	intron-variant	HDAC6	GRCh38.p7	X:48808349	CCGACTCCCACCTAG[A/G]TGCTAGACTCCCAGC	10013
rs782062932	snp	A/G	0.000529661	0.016265	upstream-variant-2KB	HDAC6	GRCh38.p7	X:48800362	TGCAAAGCCTAAGAT[A/G]TTTACTCTCTGTCCC	10013
rs782063243	snp	A/G			intron-variant	HDAC6	GRCh38.p7	X:48803981	CGGTCTGACCAACGC[A/G]ATGAAACACTGTCTC	10013
rs782063655	snp	C/T	2.29927e-05	0.00339055	intron-variant	HDAC6	GRCh38.p7	X:48816095	GGTGTTGGGGGTCCC[C/T]CCCCCTCAGGCACTA	10013
rs782067033	snp	C/G	2.39063e-05	0.00345725	intron-variant	HDAC6	GRCh38.p7	X:48820056	ATCACTTACTGCCTA[C/G]CAAAAGCCCCTACCC	10013
rs782067556	snp	C/T			intron-variant	HDAC6	GRCh38.p7	X:48804023	CAAAAATTAGTTGGG[C/T]GTGGTGGCACACACC	10013
rs782069003	snp	C/T			utr-variant-5-prime, upstream-variant-2KB	HDAC6	GRCh38.p7	X:48801412	TCACGGCGCGTCGCG[C/T]GGGAAGTCGCGGGGA	10013
rs782071628	snp	G/T	3.7303e-05	0.00431858	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48805664	GAAGAGCTGATGTTG[G/T]TTCACAGGTGAAGGC	10013
rs782073000	snp	A/G	0.00158814	0.0281345	intron-variant	HDAC6	GRCh38.p7	X:48803926	CAGCACTTTGGGGGG[A/G]CCAAGGCAGGTGGAT	10013
rs782073213	snp	C/T	2.4643e-05	0.00351011	synonymous-codon, nc-transcript-variant, intron-variant	HDAC6	GRCh38.p7	X:48817334	TTCCCAGGTTCTGAA[C/T]GGTGCTGCTGTGGTG	10013
rs782073510	snp	A/T	3.19846e-05	0.00399891	intron-variant	HDAC6	GRCh38.p7	X:48815847	TGACGGGGATTCAGA[A/T]TGAGAGGGTAGGACA	10013
rs782073877	snp	G/T	0.000529661	0.016265	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48807444	TTTAAAACACAGGTT[G/T]TGGGCTAAGTTCCTG	10013
rs782074452	snp	C/T	3.43171e-05	0.00414215	synonymous-codon, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48815007	GCCCAGCTAACCCAC[C/T]TGCTCATGGGTCTGG	10013
rs782074795	snp	G/T	2.73153e-05	0.00369553	synonymous-codon, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48823117	TGTGGTGGCCCTCAC[G/T]CAGGACCAGCCCTCA	10013
rs782076379	snp	A/G	6.91718e-05	0.00588057	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48808134	AGAAACACCGCATCC[A/G]GAGGTCAGCAACAGA	10013
rs782078648	snp	C/T	2.45513e-05	0.00350358	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HDAC6, ERAS	GRCh38.p7	X:48824567	AGATGTGAAGAACAT[C/T]GCCCACCAGAACAAG	10013
rs782078914	snp	A/G	7.86937e-05	0.00627221	missense, utr-variant-5-prime, nc-transcript-variant, intron-variant	HDAC6	GRCh38.p7	X:48802669	CACCCCCAGAACCGC[A/G]GCAGGGGCCAAGCCT	10013
rs782080607	snp	C/T			intron-variant	HDAC6	GRCh38.p7	X:48822254	AGACGGATTTCTGTA[C/T]GGCATGAAGGCAAGT	10013
rs782080815	snp	C/G			intron-variant	HDAC6	GRCh38.p7	X:48803960	TTGAGGTCAGGAGTT[C/G]GAGACCGGTCTGACC	10013
rs782082358	snp	A/G			intron-variant	HDAC6	GRCh38.p7	X:48811070	GCACTTTGGGAGGCC[A/G]AGGTGAGTGGATCAC	10013
rs782082985	snp	G/T	5.10119e-05	0.00505009	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48822940	AGAAGGACCCTCCAG[G/T]TCTAAGTTGGTCACC	10013
rs782083581	snp	A/G	0.000529661	0.016265	upstream-variant-2KB	HDAC6	GRCh38.p7	X:48800673	GCAAAGCTACTGGGC[A/G]GTGAGACCGTCAATC	10013
rs782085183	snp	C/T			intron-variant	HDAC6	GRCh38.p7	X:48819258	AACTGTGTGTGTGTA[C/T]ATGACTAGTGCAGAT	10013
rs782086474	snp	C/T			upstream-variant-2KB	HDAC6	GRCh38.p7	X:48801129	AACTACCTCATAGAA[C/T]TGTGGTTTACAACGA	10013
rs782092409	snp	C/T	2.64746e-05	0.00363822	intron-variant	HDAC6	GRCh38.p7	X:48803082	CAGTTCCCTCTGACT[C/T]AGGGCCTAAAATGGA	10013
rs782094381	snp	C/T	0.000116158	0.00762006	intron-variant	HDAC6	GRCh38.p7	X:48819865	CCTTTCTGCCATCTC[C/T]ATGTCTCTAAGTCTG	10013
rs782097607	snp	C/T	2.57762e-05	0.00358991	synonymous-codon, nc-transcript-variant, intron-variant	HDAC6	GRCh38.p7	X:48817439	TCGCCATGCCCAGAC[C/T]ATCAGTGGGCATGCC	10013
rs782099507	snp	C/T	0.000529661	0.016265	intron-variant, utr-variant-5-prime, upstream-variant-2KB	HDAC6	GRCh38.p7	X:48802474	CGGGCCGGGCGGGGC[C/T]GGGTAGAATGGCCAC	10013
rs782099901	snp	G/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48817226	CACTGCATTCCAGCC[G/T]GGGCGACAGAGCGAG	10013
rs782102121	snp	A/C			downstream-variant-500B, upstream-variant-2KB	HDAC6, ERAS	GRCh38.p7	X:48825105	CCCATCCATTGCCCC[A/C]AAAAAACTAACTGAA	10013
rs782104785	snp	A/G	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48804910	GAGGAAGAGTATTCT[A/G]GGCGGGGGTGGGGGG	10013
rs782104833	snp	A/G	0.000753579	0.0193964	intron-variant	HDAC6	GRCh38.p7	X:48819836	TGAGCCACCATGCCC[A/G]GCCCCCATCTGTCCC	10013
rs782105125	snp	G/T	7.00476e-05	0.00591768	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48824277	TGTTACTACTGTCAG[G/T]CCTATGTCCACCACC	10013
rs782105383	snp	A/G	2.36661e-05	0.00343984	intron-variant, nc-transcript-variant	HDAC6	GRCh38.p7	X:48814800	GGTTAGGCTGTGAGG[A/G]TAGGTAGCCTCATGG	10013
rs782106418	snp	C/T	9.62232e-05	0.00693559	intron-variant	HDAC6	GRCh38.p7	X:48815545	GCCCGCCCACATTCC[C/T]TGACATCATATTTTC	10013
rs782108376	snp	C/T	2.44159e-05	0.0034939	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48816594	ACAGCTTGCCACTGG[C/T]GCTGCCTGCCGCCTG	10013
rs782111501	snp	C/G			intron-variant, upstream-variant-2KB	HDAC6	GRCh38.p7	X:48801579	CCGAGGCAAGAAAAA[C/G]CTTGCACCGCAGCCC	10013
rs782112228	snp	G/T	3.01464e-05	0.0038823	intron-variant, utr-variant-3-prime	HDAC6	GRCh38.p7	X:48806733	CAGCATTTGACTTTT[G/T]ACATTGTTTTAAAGT	10013
rs782114239	snp	C/T	8.11655e-05	0.00636994	intron-variant	HDAC6	GRCh38.p7	X:48815380	TCACAACTCCTTGCC[C/T]CAGGGTGGCTACAAC	10013
rs782114269	snp	C/T			intron-variant	HDAC6	GRCh38.p7	X:48808551	GGACTGAGGCTTATA[C/T]GTTAAGAGGTCACAC	10013
rs782116929	snp	C/T	7.19131e-05	0.00599595	intron-variant	HDAC6	GRCh38.p7	X:48814603	CCCCCAAAGTGAGGC[C/T]CAGCCCCGCCCTTCT	10013
rs782118233	snp	C/G			utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	HDAC6, ERAS	GRCh38.p7	X:48824858	GCCCAGAAGGAAAGG[C/G]GGGCAGCTCAGTGGC	10013
rs782119197	in-del	-/CCTCACACA	0.000529661	0.016265	upstream-variant-2KB	HDAC6	GRCh38.p7	X:48800117	CCCATGAATCCCTGT[-/CCTCACACA]CCTCACACACCTCAC	10013
rs782119212	snp	G/T	3.04317e-05	0.00390063	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48814987	CCGCCACTCCGGCAG[G/T]GTTCGCCCAGCTAAC	10013
rs782119289	snp	C/T	2.66813e-05	0.00365238	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823506	CCCCCCCAACCTCAC[C/T]TGTGCAGGGAACTAC	10013
rs782120256	snp	A/G	6.85816e-05	0.00585543	synonymous-codon, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48824029	TTGTGGGGACTGTGG[A/G]ACAATCCAAGAGAAT	10013
rs782120699	snp	A/T	9.47306e-05	0.00688159	intron-variant, utr-variant-3-prime	HDAC6	GRCh38.p7	X:48806502	CAGGGAATGGTGGCA[A/T]TCTTGGGGTCCCCAT	10013
rs782122874	snp	A/G			intron-variant, utr-variant-3-prime, downstream-variant-500B	HDAC6	GRCh38.p7	X:48806076	AACTTTAAGAGGAGA[A/G]AAAGAGTGAGTCAGA	10013
rs782123991	snp	C/T	3.44127e-05	0.00414791	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48808127	GCTCAACAGAAACAC[C/T]GCATCCGGAGGTCAG	10013
rs782124084	snp	G/T	2.55944e-05	0.00357723	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48822818	ATTTGGGGGTGATGG[G/T]GGGAACCCAGGGAAG	10013
rs782125064	snp	C/T	3.34353e-05	0.00408859	intron-variant	HDAC6	GRCh38.p7	X:48808367	CTAGACTCCCAGCCA[C/T]CTCCCACCCTTACAG	10013
rs782125114	snp	A/G	3.15492e-05	0.0039716	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48802875	CTGATTCACAGAAGC[A/G]AAATATTAAAAAGGG	10013
rs782125309	snp	C/T	3.38627e-05	0.00411463	intron-variant	HDAC6	GRCh38.p7	X:48805620	CCACTTTATTCCTCA[C/T]CTCTCCCCAGGCCCG	10013
rs782126523	snp	G/T	2.59387e-05	0.0036012	intron-variant, upstream-variant-2KB	HDAC6, ERAS	GRCh38.p7	X:48824534	TGCCCTATTCTTGCC[G/T]CCTCCTCAGGCTCTC	10013
rs782128854	snp	A/G	1.64912e-05	0.00287147	missense, intron-variant, nc-transcript-variant	HDAC6	GRCh38.p7	X:48818344	AACGTGGCATGGAAC[A/G]GGCCCCGCATGGGTG	10013
rs782129125	snp	C/G	2.73452e-05	0.00369755	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823723	CTACTAGGAGAGGCA[C/G]CTGGAGGTCAGGACA	10013
rs782131500	snp	A/G	0.000222695	0.0105498	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823560	TGATTGGGAGTCTCA[A/G]GACCTTGGAGCTAGG	10013
rs782134796	snp	C/T	6.03045e-05	0.00549078	intron-variant	HDAC6	GRCh38.p7	X:48818120	CCCAGGTAAGGGCTG[C/T]AGTCAGGGGCCGCAG	10013
rs782137982	snp	A/G	2.38732e-05	0.00345485	synonymous-codon, nc-transcript-variant, intron-variant	HDAC6	GRCh38.p7	X:48817358	TGTGGTGCGTCCCCC[A/G]GGACACCACGCAGAG	10013
rs782138755	snp	A/G	0.00633741	0.0559334	intron-variant	HDAC6	GRCh38.p7	X:48819630	CTCACTGCCAGCTCC[A/G]CCTCCTGGGTTCATG	10013
rs782138984	in-del	-/C			intron-variant	HDAC6	GRCh38.p7	X:48811836	GTTCTTTATTTTGTT[-/C]ATTTCTGGCTTCTGG	10013
rs782139287	snp	C/T	0.000136841	0.00827054	intron-variant	HDAC6	GRCh38.p7	X:48818444	ATCGCAGGACGTATG[C/T]GACACGCCTGTGCAG	10013
rs782140204	snp	C/T	2.56548e-05	0.00358145	synonymous-codon, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48822934	AGACAGAGAAGGACC[C/T]TCCAGTTCTAAGTTG	10013
rs782141748	snp	C/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48811393	TTTTCTTGGTCCTTC[C/T]CTTTTATGCTGATGG	10013
rs782142953	snp	C/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48818529	GATGATATGAGACAG[C/T]GCATGGGTGTTTAAT	10013
rs782144824	in-del	-/GAGGGCAG	3.67863e-05	0.00428857	intron-variant	HDAC6	GRCh38.p7	X:48817284	GGAAGAAAGGAAGGT[-/GAGGGCAG]GAGGGCAGGCTGTCC	10013
rs782145413	snp	C/T	2.72409e-05	0.00369049	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48815891	CCTTTTAGCTGAGAC[C/T]GTGGAGAGGGACAAC	10013
rs782146094	snp	C/T	3.01255e-05	0.00388096	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48816522	AACCCGGGAGCTGCA[C/T]CGTGAGAGTTCCAAC	10013
rs782146543	snp	A/G	3.76854e-05	0.00434065	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823285	GGGAGGAGCCATTCT[A/G]GACCAGACCACCTCA	10013
rs782150730	snp	A/G	0.00791544	0.0624105	intron-variant	HDAC6	GRCh38.p7	X:48813973	CCATGCTCCATTTGG[A/G]CCTCCAGTGTCACAG	10013
rs782153487	snp	A/G	2.68356e-05	0.00366293	intron-variant	HDAC6	GRCh38.p7	X:48815518	GGAGGAGGGGAAAGC[A/G]GGAGCCTCACTGCCC	10013
rs782156796	snp	A/G	3.29652e-05	0.00405974	intron-variant	HDAC6	GRCh38.p7	X:48805428	TGTGACTGTGACTCC[A/G]TCTCCCCAGCTTCCC	10013
rs782157184	snp	G/T	6.61485e-05	0.00575064	intron-variant	HDAC6	GRCh38.p7	X:48808170	GATGTGATGGGGGTG[G/T]CATGGGGTGGGGTGT	10013
rs782158440	snp	C/T			intron-variant	HDAC6	GRCh38.p7	X:48803899	AGGCATGGTGGCTCA[C/T]GCCTATAATCCCAGC	10013
rs782160694	snp	C/T	2.67405e-05	0.00365644	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823496	GACCACCAGACCCCC[C/T]CAACCTCACCTGTGC	10013
rs782161108	snp	C/T	0.00105904	0.0229869	intron-variant	HDAC6	GRCh38.p7	X:48807807	CTGAGCCACCGCACC[C/T]GGCCTTTATCATTTT	10013
rs782161146	snp	A/G			intron-variant	HDAC6	GRCh38.p7	X:48813575	GAAGGATGGATGGAT[A/G]ATAGATTATTCATTT	10013
rs782161620	snp	G/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48810744	CTCCTGAGTAGCTGG[G/T]ACCACAGGTGCACAC	10013
rs782164804	snp	G/T	2.65495e-05	0.00364336	intron-variant	HDAC6	GRCh38.p7	X:48803086	TCCCTCTGACTCAGG[G/T]CCTAAAATGGATCTG	10013
rs782165694	snp	C/T	0.00211696	0.0324653	intron-variant	HDAC6	GRCh38.p7	X:48817136	AAGCGCCTGTAGTCC[C/T]AGCTACTCAGGAGGC	10013
rs782165776	snp	A/G	2.45041e-05	0.00350021	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HDAC6, ERAS	GRCh38.p7	X:48824588	CCAGAACAAGTTTGG[A/G]GAGGATATGCCCCAC	10013
rs782166983	snp	A/T	0.00158814	0.0281345	intron-variant	HDAC6	GRCh38.p7	X:48815820	TGTTTGGGTCACCTG[A/T]GTTCCAGAGTATGAC	10013
rs782168055	snp	C/T	4.98269e-05	0.00499109	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48822965	GTCACCAAGAAGGCA[C/T]CCCAACCAGCCAAAC	10013
rs782170445	snp	G/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48820839	TTTTGTTGTTGTTGT[G/T]GTTGTTGTTGTTTGT	10013
rs782173182	snp	C/T	0.000529661	0.016265	intron-variant, upstream-variant-2KB, utr-variant-5-prime	HDAC6	GRCh38.p7	X:48801959	GGTGAGTACAGCGCG[C/T]CGACGGCGGAGGCGG	10013
rs782174981	snp	A/G	4.62412e-05	0.00480816	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48824247	GTCCTCAGCTACATC[A/G]ACCTGTCAGCCTGGT	10013
rs782175804	snp	A/T	2.88251e-05	0.00379628	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48814969	CCCCCCAGGGTGAGA[A/T]GGCCGCCACTCCGGC	10013
rs782176475	snp	A/G	2.65908e-05	0.00364619	intron-variant	HDAC6	GRCh38.p7	X:48814636	CAGCGGCTCGGGACA[A/G]GTGGCTGAACATCCC	10013
rs782177881	snp	A/C			intron-variant	HDAC6	GRCh38.p7	X:48812715	GTAGGAGGTTGAGGA[A/C]GTAAACCTGTGCTAT	10013
rs782178472	snp	C/G	0.00045798	0.0151255	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	HDAC6, ERAS	GRCh38.p7	X:48824898	GAGCTGATATCATGA[C/G]GATAACATTGGCGGG	10013
rs782178851	snp	A/G	3.56837e-05	0.00422381	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48808318	GTTCACCTTCGACCA[A/G]GACCCCAGGTATACC	10013
rs782180146	in-del	-/C	5.92312e-05	0.0054417	intron-variant	HDAC6	GRCh38.p7	X:48805603	TGCCTTAACCCTTTA[-/C]CCCACTTTATTCCTC	10013
rs782182302	snp	C/T	8.39595e-05	0.00647864	intron-variant	HDAC6	GRCh38.p7	X:48818012	GGGCGTGAGTATCGT[C/T]GGTTACTGAGGTGCT	10013
rs782183158	snp	A/G/T	2.42662e-05	0.00348318	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48816605	CTGGCGCTGCCTGCC[A/G/T]CCTGGTGGAGGCTGT	10013
rs782183383	snp	A/G			intron-variant	HDAC6	GRCh38.p7	X:48803342	ATTTGGGGAGGTAGG[A/G]CTCACACTTGAAAGG	10013
rs782183697	snp	C/T	2.46612e-05	0.00351141	intron-variant, utr-variant-3-prime	HDAC6	GRCh38.p7	X:48806597	CTTTCTGGCTCCCCA[C/T]TGTCTCTCCAGAACT	10013
rs782185203	snp	A/G	2.72442e-05	0.00369072	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823539	CCCAGATATCTCCCA[A/G]TACACTGATTGGGAG	10013
rs782185823	snp	C/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48817056	AGATCGAGACCATCC[C/T]GGATAACATGGTGAA	10013
rs782186548	snp	C/G	0.000529661	0.016265	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48820439	TGCTCACTATGTGCA[C/G]AGCACTCTTCTGAGC	10013
rs782187363	snp	C/T	3.68949e-05	0.00429489	intron-variant, upstream-variant-2KB	HDAC6	GRCh38.p7	X:48802618	GTGGGGTCCTCAGGG[C/T]ACACTAGCCCCCTCA	10013
rs782188147	snp	C/T	7.41235e-05	0.00608738	intron-variant	HDAC6	GRCh38.p7	X:48803263	CCACAAAAATACACA[C/T]ACTTAGAGCCCATTA	10013
rs782189716	snp	A/G			intron-variant	HDAC6	GRCh38.p7	X:48810223	TAGGACTGCAGGCAT[A/G]TGCCACCACACCCAG	10013
rs782190620	snp	A/G	2.77897e-05	0.00372748	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48802963	GAAGCTCGGCCAAGC[A/G]ATGGAAGAAGACCTA	10013
rs782191985	snp	C/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48813688	ATCTGTTTTGCGTGT[C/T]GGTCATACTCACCCC	10013
rs782193224	snp	C/T	3.31022e-05	0.00406817	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48822909	CTCCCTCCCTGGTTC[C/T]AGAGGTAGAAGACAG	10013
rs782194728	snp	A/C	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48811777	GGGTTTTTAATACTT[A/C]ATTAATTTTTCTGGT	10013
rs782196055	snp	A/C	2.34808e-05	0.00342635	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48824154	ACCTGACACTCACAC[A/C]CCCAACCTCAGGTCT	10013
rs782196516	snp	A/T	0.000529661	0.016265	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	HDAC6, ERAS	GRCh38.p7	X:48824825	CCCATTGCCTGCTTG[A/T]GGGGCACCACTACTC	10013
rs782197065	snp	C/T	9.90704e-05	0.00703743	missense, nc-transcript-variant, intron-variant	HDAC6	GRCh38.p7	X:48802750	AGAAGTAGGCAGAAC[C/T]CCCAGTCGCCCCCTC	10013
rs782200605	snp	C/T			missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48816149	CTGCTAGCCACCACC[C/T]TGAGGTACCCCAGCG	10013
rs782201563	snp	C/G	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48821743	AAACTCCTGACCTCA[C/G]GTAACCTTCCCGCCT	10013
rs782203131	snp	C/T	4.62305e-05	0.00480761	synonymous-codon, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48824246	GGTCCTCAGCTACAT[C/T]GACCTGTCAGCCTGG	10013
rs782203780	snp	A/G	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48817113	AAAAATTAGCCGGGC[A/G]TGGCAGCAAGCGCCT	10013
rs782204492	snp	C/T	2.83813e-05	0.00376694	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48820275	CTTTCTCTTGGTCCC[C/T]CTTCCCACAGTGGGA	10013
rs782207450	snp	C/T	0.000138735	0.00832755	synonymous-codon, intron-variant, nc-transcript-variant	HDAC6	GRCh38.p7	X:48818262	TGATCATGGCACCTT[C/T]TTCCCCATGGGGGAT	10013
rs782208112	snp	C/T	2.911e-05	0.00381499	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823691	CCTCAGAATCTCAGG[C/T]CCCAGGAGAGGAGAA	10013
rs782212703	snp	C/T	9.168e-05	0.0067699	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48814524	GTCCACCACAGGTTT[C/T]GGCCAAGGCCAAGGA	10013
rs782213675	snp	A/G	4.13693e-05	0.00454785	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48816488	ACGTGGGTCATCTCC[A/G]GGCCACAGAGAAAAT	10013
rs782213865	snp	A/G	2.83966e-05	0.00376796	intron-variant	HDAC6	GRCh38.p7	X:48815500	CCGGAGGTGAGCCCC[A/G]GTGGAGGAGGGGAAA	10013
rs782214759	snp	C/G	2.30044e-05	0.00339141	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48816199	CGTCTGGAGGAGCTG[C/G]GCCTTGCCGGGCGCT	10013
rs782214899	snp	A/C	4.5809e-05	0.00478565	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48816030	GACCAAAATATGATG[A/C]ATCACTGCAACTTGT	10013
rs782216196	snp	C/T	3.4405e-05	0.00414745	intron-variant	HDAC6	GRCh38.p7	X:48818006	CTTCCAGGGCGTGAG[C/T]ATCGTCGGTTACTGA	10013
rs782216203	snp	A/G	0.000177431	0.00941721	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48815319	TCTCTTATTATCATC[A/G]TTATTATTATTCCCT	10013
rs782217493	snp	A/C	0.000636537	0.0178287	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	HDAC6, ERAS	GRCh38.p7	X:48824877	CAGCTCAGTGGCCCC[A/C]AGAGGGAGCTGATAT	10013
rs782218086	snp	C/G	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48817741	CCTCGACAGAACCCA[C/G]GTCTAGGCTCCTGAT	10013
rs782220164	snp	A/G	0.000104833	0.00723916	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48808313	ACACAGTTCACCTTC[A/G]ACCAGGACCCCAGGT	10013
rs782220797	snp	C/T	3.28553e-05	0.00405297	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48808299	ACCACGGTCAAGGAA[C/T]ACAGTTCACCTTCGA	10013
rs782221983	snp	G/T			upstream-variant-2KB	HDAC6	GRCh38.p7	X:48800557	GTGTAGGGGTTTAAA[G/T]GTCTTAGGTCTGCAA	10013
rs782224339	snp	A/G			intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48807252	TGTATCTTGGAGCCC[A/G]GTAGAACACCATTGT	10013
rs782224712	snp	A/C	2.9055e-05	0.00381138	intron-variant	HDAC6	GRCh38.p7	X:48805530	CCTTTCAGGTAAGGC[A/C]CCCAAGCCAACACTC	10013
rs782225124	snp	A/G	3.26637e-05	0.00404114	intron-variant	HDAC6	GRCh38.p7	X:48802824	TGAGGGGGAGAGGGA[A/G]CAAGTTGGTCATGCC	10013
rs782226583	snp	C/T	2.28754e-05	0.00338189	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48823950	CTGTGACACCACTGC[C/T]CTGGTGTCCCCATTT	10013
rs782227206	snp	C/T	2.49243e-05	0.00353009	intron-variant	HDAC6	GRCh38.p7	X:48822600	CACCATACCTTTCCC[C/T]CCCCTTTTCCTTAAC	10013
rs782227503	snp	C/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48804413	TCGGTCTTCTACTCT[C/T]CCAGCTGCCTTTCAC	10013
rs782229341	snp	A/G	4.82381e-05	0.00491088	intron-variant	HDAC6	GRCh38.p7	X:48824324	GACCCTTCGACACGT[A/G]CACACTCACCCCCCA	10013
rs782231028	snp	C/G	0.00105904	0.0229869	intron-variant	HDAC6	GRCh38.p7	X:48803429	GTGATACAAATGTAC[C/G]AAACAACAGACAGGG	10013
rs782232547	snp	C/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48813105	GTAGAGACAGGGTTT[C/T]GCCATGTTGGCCATG	10013
rs782232879	snp	A/C	0.000310607	0.0124582	missense, upstream-variant-2KB, nc-transcript-variant	HDAC6	GRCh38.p7	X:48801943	GTCCAATGAGTGGAG[A/C]GGTGAGTACAGCGCG	10013
rs782233489	snp	C/G	0.000529661	0.016265	upstream-variant-2KB	HDAC6	GRCh38.p7	X:48800104	GTGACCTGACCCTGC[C/G]CATGAATCCCTGTCC	10013
rs782234669	in-del	-/CGGTGGAGGAGGGGAAAG	3.29489e-05	0.00405874	intron-variant	HDAC6	GRCh38.p7	X:48815498	GCCGGAGGTGAGCCC[-/CGGTGGAGGAGGGGAAAG]CGGTGGAGGAGGGGA	10013
rs782236164	snp	C/T	0.000108189	0.00735408	intron-variant	HDAC6	GRCh38.p7	X:48820037	TCCATGTCTCTGGGT[C/T]GCCATCACTTACTGC	10013
rs782236170	snp	C/T			intron-variant	HDAC6	GRCh38.p7	X:48815715	ACTGTCTTCAGACTT[C/T]CTCTGACTTTACTGG	10013
rs782237361	snp	C/G	3.68636e-05	0.00429307	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823233	AGGAGGCTGTCGGGG[C/G]AGCCACTCCGGACCA	10013
rs782237460	snp	C/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48808493	TCTCTCCTAATTTCA[C/T]TCTGAGGCAGGGACT	10013
rs782239345	snp	G/T	1.6476e-05	0.00287014	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48803212	CATTGCCTCTGGGAT[G/T]ACAGGTGAGGCTGGG	10013
rs782240476	snp	C/T	0.000120159	0.00775017	intron-variant	HDAC6	GRCh38.p7	X:48814607	CAAAGTGAGGCCCAG[C/T]CCCGCCCTTCTGTCA	10013
rs782240693	snp	A/G	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48817880	TTGCTCAGGCCTACC[A/G]GGCAGCCCTTGGGAA	10013
rs782241054	snp	C/T	2.41002e-05	0.00347124	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48823050	TGGGGAAAGTCACCT[C/T]GGCATCATTTGGGGA	10013
rs782242286	in-del	-/T	0.000215517	0.0103784	intron-variant	HDAC6	GRCh38.p7	X:48808015	TACTCCAAGCTGTTA[-/T]TTCCTTGTCTTGCCC	10013
rs782244231	snp	G/T	2.29584e-05	0.00338802	intron-variant	HDAC6	GRCh38.p7	X:48816086	GGATGAGTAGGTGTT[G/T]GGGGTCCCTCCCCCT	10013
rs782244361	snp	C/T	5.92338e-05	0.00544182	synonymous-codon, intron-variant, nc-transcript-variant	HDAC6	GRCh38.p7	X:48818409	GCTTCCCATTGCCTA[C/T]GAGGTACAGCTCAGG	10013
rs782245142	snp	C/T			upstream-variant-2KB	HDAC6	GRCh38.p7	X:48800145	CACACAAAAGGAATA[C/T]CTCTCCTTAGGAAAA	10013
rs782246630	snp	G/T			intron-variant	HDAC6	GRCh38.p7	X:48808878	GATTTTCTCTATAGA[G/T]GTCTGAATTTTTATT	10013
rs782248305	snp	A/G	0.00105904	0.0229869	intron-variant	HDAC6	GRCh38.p7	X:48803615	TATAGAGGAAGAGAC[A/G]TTTGTACTGAAACAG	10013
rs782249002	snp	A/G	2.66553e-05	0.00365061	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48822891	GTACCCACACTCAAG[A/G]ATCTCCCTCCCTGGT	10013
rs782249918	snp	C/T	3.00445e-05	0.00387574	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48802920	CTATCCCCAATCTAG[C/T]GGAGGTAAAGAAGAA	10013
rs782251249	snp	C/T	9.80745e-05	0.00700197	intron-variant	HDAC6	GRCh38.p7	X:48815835	AGTTCCAGAGTATGA[C/T]GGGGATTCAGATTGA	10013
rs782251435	snp	A/G	0.000529661	0.016265	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48807088	GTAAAATCATGGTAC[A/G]TCTTATCATCATTGG	10013
rs782251487	snp	C/T	2.86973e-05	0.00378785	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823422	CACTGGACCAGACTA[C/T]GTCAGAGGAGGCTCC	10013
rs782252363	snp	C/G	0.00105904	0.0229869	intron-variant	HDAC6	GRCh38.p7	X:48821587	GGCTCACTGCAGCCT[C/G]TATCTCCCAGGCTCG	10013
rs782254964	snp	C/T			intron-variant	HDAC6	GRCh38.p7	X:48812839	TATTGACTTTGATGG[C/T]TCTCTTTTAGAGTCA	10013
rs782255342	snp	C/T	0.00296996	0.0384208	synonymous-codon, nc-transcript-variant, intron-variant	HDAC6	GRCh38.p7	X:48817367	TCCCCCAGGACACCA[C/T]GCAGAGCAGGATGCA	10013
rs782255932	snp	C/G	9.46566e-05	0.00687891	intron-variant	HDAC6	GRCh38.p7	X:48818209	TCCGCTTCCCACCCC[C/G]TCCCTGGCAGTGTGC	10013
rs782256417	snp	G/T	0.000529661	0.016265	intron-variant, utr-variant-3-prime, downstream-variant-500B	HDAC6	GRCh38.p7	X:48806066	ATCTGAGCTGAACTT[G/T]AAGAGGAGAAAAAGA	10013
rs782258601	snp	A/G			intron-variant	HDAC6	GRCh38.p7	X:48805001	GAAGAGACCAGTGTA[A/G]GTGAAGCGAAGCAAA	10013
rs782259162	snp	A/T	0.00105904	0.0229869	intron-variant	HDAC6	GRCh38.p7	X:48804145	CCAGCCTGGGCAACA[A/T]GAGCAAAACTCTGTC	10013
rs782259256	snp	A/G	2.33809e-05	0.00341905	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48824179	AGGTCTACTGTGGTC[A/G]TTACATCAATGGCCA	10013
rs782260538	snp	A/G	2.33609e-05	0.00341759	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48822740	GGGGCCCTGGCCTCA[A/G]TCACTGAGACCATCC	10013
rs782262355	snp	C/G	0.000529661	0.016265	intron-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	HDAC6	GRCh38.p7	X:48802056	GTCGGGTCTGGGCAG[C/G]GGGTGGAGCTGGTTG	10013
rs782263276	snp	A/G	2.41511e-05	0.0034749	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	HDAC6	GRCh38.p7	X:48806614	GTCTCTCCAGAACTC[A/G]TACTCCTGTGCCTGC	10013
rs782263709	in-del	-/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48811665	TTGGGGTAACATCTC[-/T]TTTTTTCCCTCAGCC	10013
rs782263919	snp	A/G	5.51511e-05	0.00525095	intron-variant	HDAC6	GRCh38.p7	X:48816457	GGTGCTCCTCTCTGT[A/G]CTTCCAGTGCTGAGT	10013
rs782264394	snp	A/G	4.57091e-05	0.00478042	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48816173	CCCAGCGCATCTTGC[A/G]GATCATGTGCCGTCT	10013
rs782266253	snp	G/T			intron-variant, splice-donor-variant, upstream-variant-2KB	HDAC6	GRCh38.p7	X:48802552	GGAGAATCAGATCGC[G/T]TAAGGAATGGAATCT	10013
rs782267038	snp	C/G	5.99457e-05	0.00547442	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48815482	GTCACCTGGTGCCCC[C/G]TGCCGGAGGTGAGCC	10013
rs782267992	snp	A/C			intron-variant	HDAC6	GRCh38.p7	X:48809927	AGAATCCACTTATCC[A/C]AGATCTGAAGAATCC	10013
rs782270044	snp	C/T			intron-variant	HDAC6	GRCh38.p7	X:48807811	GCCACCGCACCCGGC[C/T]TTTATCATTTTAGTG	10013
rs782271491	snp	A/C	0.000529661	0.016265	intron-variant, upstream-variant-2KB	HDAC6	GRCh38.p7	X:48802564	CGCGTAAGGAATGGA[A/C]TCTAATAGAGGGGGC	10013
rs782272771	snp	C/G			intron-variant	HDAC6	GRCh38.p7	X:48820872	GACAAGAGTCTCGCT[C/G]TGTCACCCAGGCTAG	10013
rs782273087	snp	A/G	0.000529661	0.016265	upstream-variant-2KB	HDAC6	GRCh38.p7	X:48800829	TTTAGACATGGAGTG[A/G]GAGTTGCGGGGGAGA	10013
rs782274418	snp	A/G	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48814355	GGGGAAATGAGTGGT[A/G]GAGGAAACTGGCAAC	10013
rs782274583	snp	A/G	0.000245663	0.0110802	intron-variant	HDAC6	GRCh38.p7	X:48803008	AGGGATGGTGAGCAG[A/G]GCCTGGCTGCAGTTT	10013
rs782274867	snp	A/G			missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48815016	ACCCACCTGCTCATG[A/G]GTCTGGCAGGAGGCA	10013
rs782275540	snp	G/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48818753	TGAGTATGTGCGTGT[G/T]CGACTCTGTGCAGGC	10013
rs782276634	snp	G/T	3.16196e-05	0.00397603	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48808264	TGCTCCTAGGGTCCT[G/T]ATCGTAGATTGGGAT	10013
rs782278004	snp	C/G	5.90354e-05	0.0054327	missense, intron-variant, nc-transcript-variant	HDAC6	GRCh38.p7	X:48818278	TTCCCCATGGGGGAT[C/G]AGGGTGCCAGCAGCC	10013
rs782279526	snp	C/T	0.000529661	0.016265	upstream-variant-2KB	HDAC6	GRCh38.p7	X:48801087	TAACCTCAGTTTCCT[C/T]ATCTGCAAAGCAGCC	10013
rs782282214	snp	A/G	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48804353	GCCAGGCACCCTCTT[A/G]CCTCTGGTCTGTACC	10013
rs782283126	snp	G/T	3.17204e-05	0.00398236	intron-variant	HDAC6	GRCh38.p7	X:48823652	CTTCTCTGATACATC[G/T]CTTACTTCTGCGTGT	10013
rs782283225	snp	C/T	3.30327e-05	0.0040639	intron-variant	HDAC6	GRCh38.p7	X:48802804	AGGCCCTAGACCCGC[C/T]CTGATGAGGGGGAGA	10013
rs782283433	snp	A/C			intron-variant	HDAC6	GRCh38.p7	X:48804789	GGAGGATAGTAGGAG[A/C]AAGTACAGTGGAGGA	10013
rs782284557	snp	C/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48819167	TACCAGAGTGCATGT[C/T]GCCGTTGTGGCTGTG	10013
rs782286421	snp	A/C			intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48824136	AGGGGGATGCTGACC[A/C]CCACCTGACACTCAC	10013
rs782289273	snp	C/G	2.6077e-05	0.00361079	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	HDAC6, ERAS	GRCh38.p7	X:48824630	CCCAGAATACGGTCC[C/G]TCTTCACCTTCTGAG	10013
rs782290258	snp	C/G	2.37877e-05	0.00344867	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48816223	GGGCGCTGCCTCACC[C/G]TGACACCGCGCCCTG	10013
rs782290699	snp	A/C			intron-variant	HDAC6	GRCh38.p7	X:48818472	CAGGTGGCAGCCTGG[A/C]CCTGCCTCCTTGGCA	10013
rs782295516	snp	C/T	2.3849e-05	0.0034531	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48823029	AGAAGGTTCTGGAAG[C/T]AGGCATGGGGAAAGT	10013
rs782295603	snp	C/T			intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48815321	TCTTATTATCATCAT[C/T]ATTATTATTCCCTGG	10013
rs782295739	snp	A/C			intron-variant	HDAC6	GRCh38.p7	X:48822169	TGTATGGGTTCACAG[A/C]AGTCGTCTTGTGCAG	10013
rs782296341	snp	C/G			upstream-variant-2KB	HDAC6	GRCh38.p7	X:48800923	GTTACCCGTTGGAGG[C/G]GGCAGATAGGGAGAG	10013
rs782299234	snp	C/T	2.76365e-05	0.00371719	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823447	GGCTCCAGGGGGCAC[C/T]GAGCTGATCCAAACT	10013
rs782299618	snp	C/T	0.000153799	0.00876788	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48815333	CATTATTATTATTCC[C/T]TGGTCATGTCTGGTC	10013
rs782301760	snp	C/T	7.83269e-05	0.00625758	intron-variant	HDAC6	GRCh38.p7	X:48819984	TCTGTGTCTCCATCT[C/T]TCTGACTTGCATCTC	10013
rs782302395	snp	A/G	2.29303e-05	0.00338594	intron-variant	HDAC6	GRCh38.p7	X:48816068	GTAGGCATTTGGAGG[A/G]CTGGATGAGTAGGTG	10013
rs782306373	snp	C/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48813722	GAGTGCTCATTCTCT[C/T]GCCTATAAAATAGAA	10013
rs782306531	snp	A/G	9.68793e-05	0.00695918	synonymous-codon, nc-transcript-variant, intron-variant	HDAC6	GRCh38.p7	X:48817346	GAATGGTGCTGCTGT[A/G]GTGCGTCCCCCAGGA	10013
rs782307222	snp	A/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48821768	CCGCCTCGGCCTCCC[A/T]AAGTGCTGGGATTAT	10013
rs782308787	snp	A/G	2.29166e-05	0.00338493	intron-variant	HDAC6	GRCh38.p7	X:48815657	AGTAGGAAGTGGGGT[A/G]TGGGCCTGGTGTGGG	10013
rs782309998	snp	C/T	2.34555e-05	0.0034245	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48824160	CACTCACACCCCCAA[C/T]CTCAGGTCTACTGTG	10013
rs782310029	snp	A/C	9.34056e-05	0.00683331	intron-variant	HDAC6	GRCh38.p7	X:48820068	CTACCAAAAGCCCCT[A/C]CCCTCATGCTTATAC	10013
rs782310288	snp	C/T	6.69591e-05	0.00578576	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48816511	GAGAAAATGAAAACC[C/T]GGGAGCTGCACCGTG	10013
rs782312874	snp	C/G	0.00158814	0.0281345	intron-variant, upstream-variant-2KB	HDAC6	GRCh38.p7	X:48802606	AAGGGCAGAGAGGTG[C/G]GGTCCTCAGGGCACA	10013
rs782315110	snp	C/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48811817	ATTAATGTTTTCCTC[C/T]GACGTTCTTTATTTT	10013
rs782316278	in-del	-/TTG/TTGTTG	0.0575928	0.159694	intron-variant	HDAC6	GRCh38.p7	X:48820825	TTTGGATCTGGTTTT[-/TTG/TTGTTG]TTGTTGTTGTTGTTG	10013
rs782317052	snp	A/G	3.17058e-05	0.00398144	intron-variant	HDAC6	GRCh38.p7	X:48815853	GGATTCAGATTGAGA[A/G]GGTAGGACAAACGTG	10013
rs782318981	snp	C/T	2.51143e-05	0.00354352	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48814731	CGTCCTGCTGCCAGT[C/T]GCCCTCGAGGTCCTG	10013
rs782320893	snp	A/G			intron-variant	HDAC6	GRCh38.p7	X:48821572	CAATGGCGCTATCTC[A/G]GCTCACTGCAGCCTC	10013
rs782321254	snp	A/G			intron-variant, utr-variant-3-prime, nc-transcript-variant	HDAC6	GRCh38.p7	X:48805717	GAGGAGCCTGCCCTG[A/G]ACAAACCAGGGCAAG	10013
rs782321822	snp	A/G			intron-variant	HDAC6	GRCh38.p7	X:48813201	GGTGTGAACCACTGC[A/G]CCCAGCCCTCTGGTG	10013
rs782322341	snp	A/G	2.3376e-05	0.00341869	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48814565	ATGTGCCTTGGAACC[A/G]GGTCAGCATCTACCC	10013
rs782322391	snp	A/C	0.000529661	0.016265	upstream-variant-2KB	HDAC6	GRCh38.p7	X:48801140	AGAATTGTGGTTTAC[A/C]ACGATGCCTGTCACA	10013
rs782322706	in-del	-/TTAT	0.00844089	0.0644143	intron-variant	HDAC6	GRCh38.p7	X:48810591	TCTCTCTCTTTTTTA[-/TTAT]TTATTTATTTATTTA	10013
rs782322740	snp	C/G	3.31516e-05	0.0040712	synonymous-codon, intron-variant, nc-transcript-variant	HDAC6	GRCh38.p7	X:48818268	TGGCACCTTCTTCCC[C/G]ATGGGGGATGAGGGT	10013
rs782324521	snp	A/G	2.75676e-05	0.00371255	intron-variant	HDAC6	GRCh38.p7	X:48815510	GCCCCGGTGGAGGAG[A/G]GGAAAGCGGGAGCCT	10013
rs782328442	snp	A/G	2.64943e-05	0.00363957	intron-variant	HDAC6	GRCh38.p7	X:48803083	AGTTCCCTCTGACTC[A/G]GGGCCTAAAATGGAT	10013
rs782331503	snp	C/T	2.28993e-05	0.00338365	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48816035	AAATATGATGAATCA[C/T]TGCAACTTGTGGGAC	10013
rs782332190	snp	A/G	3.74014e-05	0.00432427	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823244	GGGGGAGCCACTCCG[A/G]ACCAGACCACCTCAG	10013
rs782333041	snp	G/T	0.000168947	0.00918941	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48815324	TATTATCATCATTAT[G/T]ATTATTCCCTGGTCA	10013
rs782334032	snp	A/G	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48804376	TCTGTACCCTGACCA[A/G]CCCCTTTCCCAGAGA	10013
rs782334928	snp	C/T	4.57629e-05	0.00478324	missense, utr-variant-3-prime, nc-transcript-variant	HDAC6	GRCh38.p7	X:48806423	AATGAGGGAGAACTC[C/T]GTGTCCTAGCAGACA	10013
rs782336249	snp	C/T	0.000117092	0.00765064	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48824107	GGGCGGAGGTTGGCC[C/T]GGGAGCAAACTGCAG	10013
rs782338585	snp	A/G	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48803501	ATTAAACAGCCAACA[A/G]CAGTATGAGGTGTTT	10013
rs782339174	snp	C/G			intron-variant	HDAC6	GRCh38.p7	X:48812970	TGGAGTGCAGTGGCC[C/G]GATCTCGGCTCACTG	10013
rs782339525	snp	G/T	2.28579e-05	0.0033806	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48823954	GACACCACTGCCCTG[G/T]TGTCCCCATTTGGTG	10013
rs782340408	snp	A/G	0.000120694	0.0077674	synonymous-codon, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48823051	GGGGAAAGTCACCTC[A/G]GCATCATTTGGGGAA	10013
rs782341352	snp	C/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48804562	TTAATATCTATATCC[C/T]TTATCCCAACCTAAG	10013
rs782341889	snp	A/G	4.98958e-05	0.00499454	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48814929	CGGCAGGTGGGTTGC[A/G]TGGAGCCAGGCTGAC	10013
rs782342506	snp	A/C			intron-variant	HDAC6	GRCh38.p7	X:48824337	GTGCACACTCACCCC[A/C]CACACACACACCCCT	10013
rs782342844	snp	G/T	2.47335e-05	0.00351655	intron-variant	HDAC6	GRCh38.p7	X:48822611	TCCCTCCCCTTTTCC[G/T]TAACAAAGGGTGGCT	10013
rs782343488	snp	A/T	0.0026455	0.0362733	intron-variant	HDAC6	GRCh38.p7	X:48810622	TTTATTTATTTATTT[A/T]TTTTGAGACAAGGTC	10013
rs782343630	snp	A/G	5.36942e-05	0.00518114	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823480	TCTAGCCTCGAGCAC[A/G]GACCACCAGACCCCC	10013
rs782346257	snp	G/T	0.000529661	0.016265	intron-variant, upstream-variant-2KB, utr-variant-5-prime	HDAC6	GRCh38.p7	X:48802001	AGGCCGACCGAAGGC[G/T]GCTAGGGACTGGCTG	10013
rs782346673	snp	A/T	3.00021e-05	0.003873	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823680	TGTCCAGGGGGCCTC[A/T]GAATCTCAGGCCCCA	10013
rs782348468	snp	G/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48808496	CTCCTAATTTCACTC[G/T]GAGGCAGGGACTGTT	10013
rs782348945	snp	A/G	2.64943e-05	0.00363957	intron-variant	HDAC6	GRCh38.p7	X:48820038	CCATGTCTCTGGGTC[A/G]CCATCACTTACTGCC	10013
rs782350991	snp	C/T			missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48815959	GACCCTGGGAGCCCC[C/T]TGTGCTCCCAATCCT	10013
rs782351313	snp	A/G	2.9304e-05	0.00382768	intron-variant	HDAC6	GRCh38.p7	X:48803222	GGGATGACAGGTGAG[A/G]CTGGGTCCTCCAGGC	10013
rs782353504	snp	A/G	2.55353e-05	0.00357309	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48822939	GAGAAGGACCCTCCA[A/G]TTCTAAGTTGGTCAC	10013
rs782353677	in-del	-/T	0.238315	0.249727	intron-variant	HDAC6	GRCh38.p7	X:48819547	GTCCCCATCTGTCCC[-/T]TTTTTTTTTTTTTTG	10013
rs782354147	snp	C/T	0.000991817	0.0222469	intron-variant	HDAC6	GRCh38.p7	X:48818035	GAGGTGCTGTCTCCT[C/T]CCCAGGATCCTGATT	10013
rs782355824	snp	C/T	2.6564e-05	0.00364435	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48822897	ACACTCAAGGATCTC[C/T]CTCCCTGGTTCCAGA	10013
rs782356857	snp	C/G/T	0.000216661	0.0104061	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823532	ACTACACCCCAGATA[C/G/T]CTCCCAGTACACTGA	10013
rs782358466	snp	A/G	9.1391e-05	0.00675923	synonymous-codon, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48814988	CGCCACTCCGGCAGG[A/G]TTCGCCCAGCTAACC	10013
rs782361475	snp	A/G			upstream-variant-2KB	HDAC6	GRCh38.p7	X:48801209	GACTCCTTCCACTCA[A/G]AATATTGCGGCAGAA	10013
rs782362450	snp	G/T	2.29561e-05	0.00338785	intron-variant	HDAC6	GRCh38.p7	X:48816089	TGAGTAGGTGTTGGG[G/T]GTCCCTCCCCCTCAG	10013
rs782363354	snp	A/G	5.07945e-05	0.00503931	intron-variant	HDAC6	GRCh38.p7	X:48818417	TTGCCTACGAGGTAC[A/G]GCTCAGGATAGATCG	10013
rs782364905	snp	A/G	2.52761e-05	0.00355492	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48815920	ACATGGAGGAGGACA[A/G]TGTAGAGGAGAGCGA	10013
rs782365359	snp	A/G	2.51215e-05	0.00354403	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48814728	GCACGTCCTGCTGCC[A/G]GTCGCCCTCGAGGTC	10013
rs782368786	snp	A/G	0.000529661	0.016265	intron-variant, utr-variant-3-prime, downstream-variant-500B	HDAC6	GRCh38.p7	X:48806106	ATGAAGAGGGTGACT[A/G]AGGGAAGGGAAGAAC	10013
rs782369174	snp	C/T	0.000114679	0.00757141	intron-variant	HDAC6	GRCh38.p7	X:48805412	AGTGTCCTCATGCAT[C/T]TGTGACTGTGACTCC	10013
rs782372342	snp	C/T	2.58505e-05	0.00359508	intron-variant, upstream-variant-2KB	HDAC6, ERAS	GRCh38.p7	X:48824536	CCCTATTCTTGCCTC[C/T]TCCTCAGGCTCTCCT	10013
rs782372385	snp	A/G	3.4462e-05	0.00415088	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48808128	CTCAACAGAAACACC[A/G]CATCCGGAGGTCAGC	10013
rs782373936	snp	A/G	0.00105904	0.0229869	intron-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	HDAC6	GRCh38.p7	X:48802161	CCGGTCCGGCCCGAT[A/G]AGGGGTGGAGTTAAG	10013
rs782374198	snp	A/G	3.29848e-05	0.00406095	intron-variant	HDAC6	GRCh38.p7	X:48815837	TTCCAGAGTATGACG[A/G]GGATTCAGATTGAGA	10013
rs782374661	snp	C/T	0.000143246	0.00846182	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48816474	TTCCAGTGCTGAGTA[C/T]GTGGGTCATCTCCGG	10013
rs782375375	snp	A/C	0.000529661	0.016265	upstream-variant-2KB	HDAC6	GRCh38.p7	X:48801007	TATTATCACAACTTT[A/C]CAGATGAGGAAACGG	10013
rs782375949	snp	A/G			intron-variant	HDAC6	GRCh38.p7	X:48818683	TTCTGACTATGCACC[A/G]ATGGCCCGTGTCCTG	10013
rs782380536	snp	A/G/T	9.24116e-05	0.00679694	synonymous-codon, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48824228	AAATTCTGGACACCC[A/G/T]CTGGTCCTCAGCTAC	10013
rs782383035	snp	A/G	2.28222e-05	0.00337795	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48814494	GTTCTGGCCCCACCT[A/G]AAGGCCTCTAACTGG	10013
rs782383335	snp	A/G	8.18978e-05	0.00639861	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823453	AGGGGGCACCGAGCT[A/G]ATCCAAACTCCTCTA	10013
rs782384780	in-del	-/C	2.47853e-05	0.00352023	frameshift-variant, upstream-variant-2KB, nc-transcript-variant	HDAC6, ERAS	GRCh38.p7	X:48824602	GGAGGATATGCCCCA[-/C]CCCACACTAAGCCCC	10013
rs782385231	snp	A/G	4.7349e-05	0.00486542	intron-variant, utr-variant-3-prime	HDAC6	GRCh38.p7	X:48806362	TCATCTCCCATCTGT[A/G]TCTAGCCTAGAATAT	10013
rs782385832	snp	A/T	2.29526e-05	0.00338759	synonymous-codon, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48823936	GGCCATATTTTATGC[A/T]GTGACACCACTGCCC	10013
rs782386516	snp	A/G			upstream-variant-2KB	HDAC6	GRCh38.p7	X:48800984	GCCATTCTGGCCCTG[A/G]GCACTATTATTATCA	10013
rs782388052	snp	C/T	0.00105904	0.0229869	intron-variant	HDAC6	GRCh38.p7	X:48817120	AGCCGGGCGTGGCAG[C/T]AAGCGCCTGTAGTCC	10013
rs782388111	snp	C/T	0.00211696	0.0324653	intron-variant	HDAC6	GRCh38.p7	X:48819029	GGTGTGAGCACCGCT[C/T]TGTCACCCTGGGCGC	10013
rs782393826	snp	A/G	0.000177475	0.0094184	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48816524	CCCGGGAGCTGCACC[A/G]TGAGAGTTCCAACTT	10013
rs782395249	snp	A/G	3.41705e-05	0.00413329	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48823196	GCCATTGGGGGAGCC[A/G]TGCTGGGCCAGACCA	10013
rs782396695	snp	C/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48819186	GTTGTGGCTGTGTGG[C/T]GATGGCATGTGTATG	10013
rs782396821	snp	A/G/T	4.89437e-05	0.00494671	intron-variant	HDAC6	GRCh38.p7	X:48815540	TCACTGCCCGCCCAC[A/G/T]TTCCTTGACATCATA	10013
rs782397073	snp	C/G	2.86041e-05	0.0037817	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823696	GAATCTCAGGCCCCA[C/G]GAGAGGAGAACCTAC	10013
rs782398421	snp	A/G/T	6.98243e-05	0.00590824	intron-variant	HDAC6	GRCh38.p7	X:48815693	CGTGGGATGAGCCCT[A/G/T]GGGGAGACTGTCTTC	10013
rs782399618	snp	A/G	2.49482e-05	0.00353178	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48822801	GGGTCATGAGTGAGT[A/G]GATTTGGGGGTGATG	10013
rs782401214	snp	A/G	0.000249885	0.011175	intron-variant	HDAC6	GRCh38.p7	X:48818013	GGCGTGAGTATCGTC[A/G]GTTACTGAGGTGCTG	10013
rs782401676	snp	C/T			utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	HDAC6, ERAS	GRCh38.p7	X:48824910	TGAGGATAACATTGG[C/T]GGGAGGGGAGTTAAC	10013
rs782402831	snp	A/G	0.000161698	0.00899016	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48816208	GAGCTGGGCCTTGCC[A/G]GGCGCTGCCTCACCC	10013
rs782404827	snp	C/T	0.00105904	0.0229869	intron-variant	HDAC6	GRCh38.p7	X:48820934	CCTCCACCTCCCGGC[C/T]TCAAGTGATCCTCCC	10013
rs782406258	snp	C/T	0.00317376	0.039709	intron-variant	HDAC6	GRCh38.p7	X:48810785	AGCTAATTTTTTAAT[C/T]TTTTGTAGAGATGGG	10013
rs782406744	snp	A/G	2.29421e-05	0.00338682	intron-variant	HDAC6	GRCh38.p7	X:48816076	TTGGAGGGCTGGATG[A/G]GTAGGTGTTGGGGGT	10013
rs782409624	snp	A/G	4.62968e-05	0.00481106	intron-variant	HDAC6	GRCh38.p7	X:48815688	GTGGACGTGGGATGA[A/G]CCCTGGGGGAGACTG	10013
rs782410300	snp	C/T	4.78029e-05	0.00488868	intron-variant	HDAC6	GRCh38.p7	X:48824311	TGGGCCCTGGGTAGA[C/T]CCTTCGACACGTGCA	10013
rs782410400	snp	A/G	0.000847099	0.0205629	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48815339	TATTATTCCCTGGTC[A/G]TGTCTGGTCCTTTCC	10013
rs782411267	snp	C/G	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48808652	GGTTAGAGTGAACCT[C/G]AAATTACTGCTTTAT	10013
rs782411797	snp	C/T	0.00158814	0.0281345	intron-variant	HDAC6	GRCh38.p7	X:48813616	AGTCAGAATTAAGCC[C/T]TCCCATGGCCCCTTG	10013
rs782412068	snp	C/T	9.22105e-05	0.00678946	intron-variant	HDAC6	GRCh38.p7	X:48820005	CTTGCATCTCCATGT[C/T]TTCATTTGTCCTTTT	10013
rs782412155	snp	C/T	7.89531e-05	0.00628254	intron-variant	HDAC6	GRCh38.p7	X:48808335	ACCCCAGGTATACCC[C/T]GACTCCCACCTAGGT	10013
rs782413222	snp	C/T	2.77824e-05	0.00372699	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823711	GGAGAGGAGAACCTA[C/T]TAGGAGAGGCAGCTG	10013
rs782414761	snp	C/G	6.97922e-05	0.00590688	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48808072	CAGTCTTATGGATGG[C/G]TATTGCATGTTCAAC	10013
rs782414993	snp	C/G			intron-variant	HDAC6	GRCh38.p7	X:48807993	CTGCAGAGGAGGACC[C/G]CTCACATACTCCAAG	10013
rs782415213	snp	C/T	5.70215e-05	0.00533924	synonymous-codon, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48814973	CCAGGGTGAGATGGC[C/T]GCCACTCCGGCAGGG	10013
rs782415406	snp	C/G/T	2.52615e-05	0.00355388	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48822807	TGAGTGAGTGGATTT[C/G/T]GGGGTGATGGGGGGA	10013
rs782417389	snp	A/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48817985	CCAGGGGTCTAGCCC[A/T]GCCCTCTTCCAGGGC	10013
rs782419695	snp	G/T	0.000441258	0.014847	intron-variant	HDAC6	GRCh38.p7	X:48817284	AGGAAGAAAGGAAGG[G/T]GAGGGCAGGCTGTCC	10013
rs782420490	snp	C/T	0.000123077	0.00784368	intron-variant	HDAC6	GRCh38.p7	X:48805606	CTTAACCCTTTACCC[C/T]ACTTTATTCCTCATC	10013
rs782420712	snp	A/C	0.000529661	0.016265	upstream-variant-2KB	HDAC6	GRCh38.p7	X:48800127	CCCTGTCCTCACACA[A/C]CTCACACAAAAGGAA	10013
rs782423190	snp	G/T	2.51956e-05	0.00354925	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48823084	GTCCACTCCAGGCCA[G/T]ACTAACTCAGAGACA	10013
rs782423251	snp	G/T	0.000529661	0.016265	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48807164	GTTTTTAACCACAAA[G/T]GGTAGTAACATGACA	10013
rs782423724	snp	A/G	2.64792e-05	0.00363853	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823762	TCGATGCTGATGCAG[A/G]GATCTAGGGGCCTCA	10013
rs782424527	snp	C/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48811680	CTTTTTTCCCTCAGC[C/T]TTTCCAAAGTGTATC	10013
rs782426162	snp	C/G	1.81276e-05	0.00301056	intron-variant, upstream-variant-2KB	HDAC6	GRCh38.p7	X:48802630	GGGCACACTAGCCCC[C/G]TCACATACCCACGCT	10013
rs782427575	snp	A/G	1.79926e-05	0.00299933	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48815083	CGTCCCTCAGCCTGT[A/G]GATCCTGGAGGGCTT	10013
rs782430389	snp	A/G	2.76155e-05	0.00371578	intron-variant	HDAC6	GRCh38.p7	X:48824499	CAGCCGAGGTAGAGG[A/G]GTCCTCACTCTCTCT	10013
rs782430393	snp	C/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48817015	AGCACTTTGGGAGGC[C/T]GAGGTGGGCAGATCA	10013
rs782431015	snp	C/G	2.33035e-05	0.00341339	intron-variant, nc-transcript-variant	HDAC6	GRCh38.p7	X:48814824	CTCATGGAGTCTGTT[C/G]CCCCTTCAGTTCCAG	10013
rs782431087	snp	A/G	2.22774e-05	0.0033374	intron-variant, utr-variant-3-prime, nc-transcript-variant	HDAC6	GRCh38.p7	X:48805716	GGAGGAGCCTGCCCT[A/G]GACAAACCAGGGCAA	10013
rs782431499	snp	A/G	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48823622	AGGTAGGGGCAAGAA[A/G]GGGCAAGAATCGGGC	10013
rs782435961	snp	A/G	0.000385282	0.0138742	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	HDAC6, ERAS	GRCh38.p7	X:48824911	GAGGATAACATTGGC[A/G]GGAGGGGAGTTAACT	10013
rs782438091	snp	C/G	5.38344e-05	0.0051879	intron-variant	HDAC6	GRCh38.p7	X:48814652	GTGGCTGAACATCCC[C/G]CATCACACTCCTGTG	10013
rs782438974	snp	A/G	3.29462e-05	0.00405857	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48815954	GGAAGGACCCTGGGA[A/G]CCCCCTGTGCTCCCA	10013
rs782439377	snp	A/T	2.3116e-05	0.00339963	synonymous-codon, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48814860	GCTGGTCCTGGTGGC[A/T]GCTGGATTTGATGCC	10013
rs782440465	snp	A/C	3.29294e-05	0.00405754	intron-variant	HDAC6	GRCh38.p7	X:48808239	CTTGCACAGAGTCCC[A/C]TCTCTCTGCTGCTCC	10013
rs782443750	snp	A/G			intron-variant	HDAC6	GRCh38.p7	X:48807527	TTTATTTATTTATTT[A/G]TTTTGAGACGGAGTC	10013
rs782443971	snp	C/T	2.28715e-05	0.0033816	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48814462	TATTTCTCCATCCAC[C/T]GCTACGAGCAGGGTA	10013
rs782444793	snp	A/C			intron-variant	HDAC6	GRCh38.p7	X:48811902	GATCTCATTTCATCT[A/C]TACCTGTACCCACTG	10013
rs782446302	snp	G/T	1.67654e-05	0.00289524	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48820287	CCCTCTTCCCACAGT[G/T]GGAGGGTAGTTTGGA	10013
rs782446410	snp	C/T	3.18471e-05	0.00399031	intron-variant	HDAC6	GRCh38.p7	X:48823639	GGCAAGAATCGGGCT[C/T]CTCTGATACATCTCT	10013
rs782448484	snp	A/C	2.53791e-05	0.00356215	intron-variant, utr-variant-3-prime	HDAC6	GRCh38.p7	X:48806563	GCTGAGTGGATAGGG[A/C]TGTTCTCTCCCTTAC	10013
rs782448638	snp	C/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48814378	CTGGCAACTGTTGGG[C/T]TGGGGGTGTCTATGG	10013
rs782449481	snp	A/C	3.22747e-05	0.004017	intron-variant, utr-variant-3-prime	HDAC6	GRCh38.p7	X:48806745	TTTTACATTGTTTTA[A/C]AGTCCTTCCTTCAAG	10013
rs782449862	snp	A/C	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48807961	TCCAGGATTAGAGAG[A/C]AGGGGACAGTCTGTC	10013
rs782450059	snp	A/G			intron-variant	HDAC6	GRCh38.p7	X:48804594	CTAACTTACTATGGG[A/G]AAAAGACTTCTTTTA	10013
rs782450419	snp	A/C	2.35264e-05	0.00342967	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48824290	AGGCCTATGTCCACC[A/C]CCAGGTGGGCCCTGG	10013
rs782451640	snp	A/G	4.78166e-05	0.00488938	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48823008	AGCGGATGACCACAC[A/G]AGAAAAGAAGGTTCT	10013
rs782453641	snp	A/G			intron-variant	HDAC6	GRCh38.p7	X:48814310	TTAATGGGGAAATTA[A/G]TGAATGAGAGAATGA	10013
rs782457060	snp	A/C/T	0.00102823	0.0226511	missense, nc-transcript-variant, utr-variant-3-prime	HDAC6	GRCh38.p7	X:48822701	CCACCACCCCTGCTG[A/C/T]CCCTGCCACGGCCCC	10013
rs782457576	snp	G/T	3.60646e-05	0.00424629	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823351	TACCTCAGAGGAGGC[G/T]GTAGGAGGAGCTACA	10013
rs782458401	snp	A/G	4.14079e-05	0.00454997	intron-variant	HDAC6	GRCh38.p7	X:48808343	TATACCCCGACTCCC[A/G]CCTAGGTGCTAGACT	10013
rs782459429	snp	A/G	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48822472	CTATCTTAAAGGTGT[A/G]GGTTCTGTTCACTTG	10013
rs782460263	snp	A/G	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48821427	TGAACTCCTGACCTC[A/G]TGATCCACCTGCCTC	10013
rs782461740	snp	A/G	4.65886e-05	0.00482619	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48824096	GGAAGGGGATGGGGC[A/G]GAGGTTGGCCCGGGA	10013
rs782463497	snp	A/G	9.75229e-05	0.00698226	intron-variant	HDAC6	GRCh38.p7	X:48819974	GTCTCCAGGTTCTGT[A/G]TCTCCATCTCTCTGA	10013
rs782464963	in-del	-/T	0.0217041	0.101887	intron-variant	HDAC6	GRCh38.p7	X:48803108	TGGATCTGTGTCTCC[-/T]TTTTTTTTTTCCTCT	10013
rs782466350	snp	C/T	0.000336793	0.0129724	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48814914	GCAGGCTCCCTGGGG[C/T]GGCAGGTGGGTTGCA	10013
rs782469771	snp	C/T	2.98748e-05	0.00386478	synonymous-codon, intron-variant, nc-transcript-variant	HDAC6	GRCh38.p7	X:48818352	ATGGAACGGGCCCCG[C/T]ATGGGTGATGCTGAC	10013
rs782470447	snp	A/G/T	0.000158554	0.00890249	intron-variant	HDAC6	GRCh38.p7	X:48816675	GAGGACCTGGGGGGA[A/G/T]TGGAAAAAGAGAGCC	10013
rs782470550	snp	A/G	2.29381e-05	0.00338652	intron-variant	HDAC6	GRCh38.p7	X:48815666	TGGGGTGTGGGCCTG[A/G]TGTGGGGTGGACGTG	10013
rs782471125	snp	A/G	3.1082e-05	0.00394208	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48802895	ATTAAAAAGGGAGCC[A/G]TTCCCCGCTCTATCC	10013
rs782471250	snp	A/G/T	0.000338897	0.0130128	intron-variant	HDAC6	GRCh38.p7	X:48818010	CAGGGCGTGAGTATC[A/G/T]TCGGTTACTGAGGTG	10013
rs782473082	snp	C/T	7.08483e-05	0.0059514	intron-variant	HDAC6	GRCh38.p7	X:48814407	GGGGATTGACTTCTC[C/T]AACTCTCTTACCTCT	10013
rs782474120	snp	G/T	4.75387e-05	0.00487515	intron-variant	HDAC6	GRCh38.p7	X:48816312	GATTCCCAGGACTGT[G/T]GATGAGGTCTCAGGG	10013
rs782476356	snp	A/G			intron-variant	HDAC6	GRCh38.p7	X:48809936	TTATCCAAGATCTGA[A/G]GAATCCAATTTAGGT	10013
rs782477252	snp	A/G	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48817846	GACCCAGAAGAGCCC[A/G]GGGCCCAGCCCCGAG	10013
rs782478749	in-del	-/G			upstream-variant-2KB	HDAC6	GRCh38.p7	X:48800920	TGGTTACCCGTTGGA[-/G]GGGGGCAGATAGGGA	10013
rs782479243	snp	A/G			intron-variant, upstream-variant-2KB	HDAC6	GRCh38.p7	X:48801656	TGGCGTAGCACGCCG[A/G]CGCACCGCCCCGTCG	10013
rs782479985	snp	A/G	0.000132654	0.00814306	intron-variant	HDAC6	GRCh38.p7	X:48814630	TTCTGTCAGCGGCTC[A/G]GGACAGGTGGCTGAA	10013
rs782480765	snp	G/T	3.36836e-05	0.00410374	intron-variant	HDAC6	GRCh38.p7	X:48808220	CCAGATTCACCTTGA[G/T]CTCCTTGCACAGAGT	10013
rs782481901	snp	G/T	2.50022e-05	0.0035356	intron-variant, utr-variant-3-prime	HDAC6	GRCh38.p7	X:48806589	CTTACTCCCTTTCTG[G/T]CTCCCCACTGTCTCT	10013
rs782482423	snp	A/G	2.49725e-05	0.0035335	missense, upstream-variant-2KB, nc-transcript-variant	HDAC6, ERAS	GRCh38.p7	X:48824608	ATATGCCCCACCCAC[A/G]CTAAGCCCCAGAATA	10013
rs782482870	snp	C/T	0.000491642	0.015671	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48815270	CAGTGAGGCACCCTT[C/T]TAAGTTCCTTGTTGC	10013
rs782483063	snp	A/C	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48814313	ATGGGGAAATTAATG[A/C]ATGAGAGAATGAACG	10013
rs782483173	snp	A/C	2.35327e-05	0.00343013	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48824135	CAGGGGGATGCTGAC[A/C]CCCACCTGACACTCA	10013
rs782485395	snp	A/G	0.00012343	0.00785492	intron-variant	HDAC6	GRCh38.p7	X:48816442	CCTCACTGTCCTGCG[A/G]GTGCTCCTCTCTGTG	10013
rs782486536	in-del	-/AGGGGCAAGA	3.29788e-05	0.00406058	intron-variant	HDAC6	GRCh38.p7	X:48823610	TCACCACACCCAGGT[-/AGGGGCAAGA]AGGGGCAAGAAGGGG	10013
rs782487564	snp	A/G	3.2975e-05	0.00406035	intron-variant	HDAC6	GRCh38.p7	X:48802837	GAGCAAGTTGGTCAT[A/G]CCCTGGACTCTGACC	10013
rs782487722	snp	C/T	9.19329e-05	0.00677923	intron-variant	HDAC6	GRCh38.p7	X:48818171	AGCACCTCAGGGGTA[C/T]TGGAGCCCCTAACCA	10013
rs782488384	snp	C/T			intron-variant	HDAC6	GRCh38.p7	X:48809189	AGGATGAATTTCTAA[C/T]AGTGGGTTGCTTGGG	10013
rs782488546	snp	A/G	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48810261	TTTAAATTATTTGTA[A/G]AGACAGGGTCTCACT	10013
rs782490423	snp	G/T	0.000529661	0.016265	upstream-variant-2KB	HDAC6	GRCh38.p7	X:48800818	CAGAGCTGACATTTA[G/T]ACATGGAGTGGGAGT	10013
rs782493528	snp	A/G	7.69201e-05	0.00620114	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48815069	GAGTGACTCACCTTC[A/G]TCCCTCAGCCTGTGG	10013
rs782494247	snp	A/G			intron-variant, utr-variant-3-prime	HDAC6	GRCh38.p7	X:48806817	AGAATCCAAAGGTAA[A/G]AAAGAGAATATAATT	10013
rs782494263	snp	C/T	2.60105e-05	0.00360619	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48823804	AGCTCAGGGAGAGGC[C/T]GGGACTGTGGCTTCC	10013
rs782495342	snp	G/T	0.000529661	0.016265	intron-variant, utr-variant-3-prime	HDAC6	GRCh38.p7	X:48806937	CAAAGTCTTATTCAA[G/T]AAATAAATACCATAT	10013
rs782495768	in-del	-/T	0.194041	0.243657	intron-variant	HDAC6	GRCh38.p7	X:48810071	GTTATCTTGGTGTTC[-/T]TTTTTTTTTTTTTTT	10013
rs782495985	snp	C/T	7.9447e-05	0.00630216	synonymous-codon, intron-variant, nc-transcript-variant	HDAC6	GRCh38.p7	X:48818244	TGTGTCCCTGCACCG[C/T]TATGATCATGGCACC	10013
rs782497046	snp	C/T	8.08228e-05	0.00635648	intron-variant, utr-variant-3-prime, nc-transcript-variant	HDAC6	GRCh38.p7	X:48805687	GTGAAGGCTTGGGAG[C/T]CTTGTAGGGATGGGG	10013
rs782497379	snp	A/G	8.70663e-05	0.00659739	intron-variant	HDAC6	GRCh38.p7	X:48817998	CCAGCCCTCTTCCAG[A/G]GCGTGAGTATCGTCG	10013
rs782501423	snp	G/T	3.28316e-05	0.00405151	intron-variant	HDAC6	GRCh38.p7	X:48817502	TCCTGATCCTTGTGG[G/T]GACCTGGATGCTCCC	10013
rs782504591	snp	A/G	3.24338e-05	0.00402689	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48823169	ACTCTGGCCCAGACC[A/G]TTTCTGAGGCAGCCA	10013
rs782505432	snp	A/G	5.12361e-05	0.00506117	intron-variant	HDAC6	GRCh38.p7	X:48816662	GGGCTGGGGAGAGGA[A/G]GACCTGGGGGGAATG	10013
rs782506012	snp	A/G	4.57671e-05	0.00478346	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48816185	TGCGGATCATGTGCC[A/G]TCTGGAGGAGCTGGG	10013
rs782509175	snp	A/G	3.30033e-05	0.00406209	intron-variant	HDAC6	GRCh38.p7	X:48823629	GGCAAGAAGGGGCAA[A/G]AATCGGGCTTCTCTG	10013
rs782509715	snp	A/G	7.23406e-05	0.00601374	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48814915	CAGGCTCCCTGGGGC[A/G]GCAGGTGGGTTGCAT	10013
rs782509940	snp	C/T	0.000395023	0.0140483	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48815305	CATGTGGTATGCACT[C/T]TCTTATTATCATCAT	10013
rs782511194	snp	C/T	5.61829e-05	0.00529984	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48815401	TGGCTACAACCTCCG[C/T]GCCCTGGCTGAAGGC	10013
rs782512413	in-del	-/T	9.89866e-05	0.00703445	intron-variant	HDAC6	GRCh38.p7	X:48822610	TCCCTCCCCTTTTCC[-/T]TTAACAAAGGGTGGC	10013
rs782514523	snp	A/G	0.000225928	0.0106261	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	HDAC6, ERAS	GRCh38.p7	X:48824653	CTTCTGAGGCCCACG[A/G]TAGACCAGCTGTAGC	10013
rs782515133	snp	A/T	0.0585734	0.160798	intron-variant	HDAC6	GRCh38.p7	X:48804175	CTCAAAAAGTAAAAA[A/T]AAAAAAAAAAAAAGT	10013
rs782515550	snp	C/T	5.67086e-05	0.00532458	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48805510	CCTCCTAGATCGCTG[C/T]GTGTCCTTTCAGGTA	10013
rs782517179	snp	A/G	0.000132979	0.00815302	intron-variant	HDAC6	GRCh38.p7	X:48819958	GCTTTTGTGTCTCCT[A/G]GTCTCCAGGTTCTGT	10013
rs782518317	snp	A/G			upstream-variant-2KB	HDAC6	GRCh38.p7	X:48800235	ACTACAGCACAGATC[A/G]GCAAACTATGGCATT	10013
rs782519094	snp	C/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48812647	TCCTTTCCACTCTCT[C/T]TTTCTGGGTTGCTGT	10013
rs782519241	snp	A/G	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48822393	GCTTTTATCAGTATT[A/G]TTATCTTGCACTTTA	10013
rs782523726	snp	A/G	2.61856e-05	0.0036183	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48803187	GTTGGATGAGCAGTT[A/G]AATGAATTCCATTGC	10013
rs782528685	snp	A/C			intron-variant	HDAC6	GRCh38.p7	X:48809227	GTCAGCATACTTTAA[A/C]GTCTGGTATACACTG	10013
rs782528830	in-del	-/T	0.00211696	0.0324653	intron-variant, upstream-variant-2KB	HDAC6	GRCh38.p7	X:48801619	CCGCCGGCGCCTGCC[-/T]TTTACGTAGGCGCAG	10013
rs782530262	snp	A/T	2.40258e-05	0.00346588	intron-variant	HDAC6	GRCh38.p7	X:48824320	GGTAGACCCTTCGAC[A/T]CGTGCACACTCACCC	10013
rs782530598	snp	C/G	4.96069e-05	0.00498006	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48815408	AACCTCCGCGCCCTG[C/G]CTGAAGGCGTCAGTG	10013
rs782531003	snp	A/G			intron-variant	HDAC6	GRCh38.p7	X:48815509	AGCCCCGGTGGAGGA[A/G]GGGAAAGCGGGAGCC	10013
rs782534073	snp	A/G			missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48814463	ATTTCTCCATCCACC[A/G]CTACGAGCAGGGTAG	10013
rs782534324	snp	C/T	4.19754e-05	0.00458104	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48808048	GCCTCCTGGACATCA[C/T]GCCCAGCACAGTCTT	10013
rs782534516	snp	A/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48803329	CTGGAAGCAGATGAT[A/T]TGGGGAGGTAGGGCT	10013
rs782535069	in-del	-/T	0.000140531	0.00838127	intron-variant, utr-variant-3-prime	HDAC6	GRCh38.p7	X:48806754	TTTTAAAGTCCTTCC[-/T]TTCAAGTGTAAAATG	10013
rs782535184	snp	C/T	2.52118e-05	0.00355039	intron-variant, utr-variant-3-prime	HDAC6	GRCh38.p7	X:48806578	CTGTTCTCTCCCTTA[C/T]TCCCTTTCTGGCTCC	10013
rs782535626	snp	C/G	7.0927e-05	0.0059547	intron-variant	HDAC6	GRCh38.p7	X:48805422	TGCATCTGTGACTGT[C/G]ACTCCATCTCCCCAG	10013
rs782535708	in-del	-/A			intron-variant	HDAC6	GRCh38.p7	X:48816954	GTGAGACCCTGTGTC[-/A]AAAAAAAAAAAAGGT	10013
rs782539433	snp	A/C	1.64806e-05	0.00287054	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48802910	GTTCCCCGCTCTATC[A/C]CCAATCTAGCGGAGG	10013
rs782539721	snp	C/G/T	0.000194661	0.00986407	intron-variant	HDAC6	GRCh38.p7	X:48818196	TAACCAGCCATGGTC[C/G/T]GCTTCCCACCCCCTC	10013
rs782541774	snp	C/T	3.34091e-05	0.00408698	missense, intron-variant, nc-transcript-variant	HDAC6	GRCh38.p7	X:48818398	CATCGCCTGGTGCTT[C/T]CCATTGCCTACGAGG	10013
rs782542834	snp	C/G/T	3.91698e-05	0.00442534	intron-variant, utr-variant-3-prime, nc-transcript-variant	HDAC6	GRCh38.p7	X:48805678	GGTTCACAGGTGAAG[C/G/T]CTTGGGAGCCTTGTA	10013
rs782543775	snp	C/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48804018	AAATACAAAAATTAG[C/T]TGGGCGTGGTGGCAC	10013
rs782545709	snp	A/T	6.73469e-05	0.00580249	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48815446	CCACACCCTTCTGGG[A/T]GACCCTTGCCCCATG	10013
rs782547023	snp	C/G	8.6179e-05	0.0065637	synonymous-codon, nc-transcript-variant, intron-variant	HDAC6	GRCh38.p7	X:48802698	CTCCTCAACTATGAC[C/G]TCAACCGGCCAGGAT	10013
rs782547427	snp	A/C			intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48815102	CCTGGAGGGCTTAAG[A/C]ACGAAGCTTTCAAGT	10013
rs782547507	snp	A/G	3.07598e-05	0.0039216	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48823145	TCAGAGGCAGCCACA[A/G]GGGGAGCCACTCTGG	10013
rs782547787	snp	C/T			intron-variant	HDAC6	GRCh38.p7	X:48812228	ATATATTCAGTGCAT[C/T]CTTCCTTATTAACAA	10013
rs782552897	snp	C/T	0.000529661	0.016265	intron-variant, upstream-variant-2KB	HDAC6	GRCh38.p7	X:48801715	AGCTGGCGTAGCACG[C/T]CGACGCACCGCCCCG	10013
rs782554974	snp	A/G	2.67705e-05	0.00365849	intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48822884	GGTGACAGTACCCAC[A/G]CTCAAGGATCTCCCT	10013
rs782556369	snp	C/G	5.08932e-05	0.0050442	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48803169	GGCTGGCACTGGCTT[C/G]GTGTTGGATGAGCAG	10013
rs782556836	snp	C/T	0.00083091	0.0203658	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	HDAC6, ERAS	GRCh38.p7	X:48824783	CTTTTAAGAGAACTG[C/T]GACGATTAATTGTGG	10013

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