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

KAT2B

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs113011713	snp	C/T	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20088865	CTTCTAGTAGTTTTA[C/T]AGTTTCAGGTCTATA	8850
rs113018260	snp	G/T	0.5	0	intron-variant	KAT2B	GRCh38.p7	3:20042169	GACAAACTCCCAAGT[G/T]ATGCTATGCTAGTCC	8850
rs113051421	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20118748	AAAAAAAAAAAAAAA[A/G]AGAGAGAGCGAACTA	8850
rs113053760	snp	A/G	0.5	0	intron-variant	KAT2B	GRCh38.p7	3:20043804	CTGTGGTTCTCTCTC[A/G]GCTTGTTTCTGCACT	8850
rs113073514	snp	C/T	0.5	0	intron-variant	KAT2B	GRCh38.p7	3:20079267	TGGAGTGCAATGGTG[C/T]AATCTCGGCTCACTG	8850
rs113083144	in-del	-/G	0.0150606	0.0854603	intron-variant	KAT2B	GRCh38.p7	3:20066330	ATCTGCATGTCCTTA[-/G]ACTGATCACATCTGC	8850
rs113149969	snp	C/G			missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20040635	GCTCGGGCGCCTGCG[C/G]TCCGGCGACGGCAGT	8850
rs113171361	snp	A/T			synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20040636	CTCGGGCGCCTGCGG[A/T]CCGGCGACGGCAGTG	8850
rs113186683	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20136275	TAAGCTTTGTCACTG[A/G]AAAAACTTGATATTA	8850
rs113210788	snp	C/T	0.444444	0.157135	intron-variant	KAT2B	GRCh38.p7	3:20107385	CATTTCAGCTGGGAG[C/T]GGTGGCCCACGCCAG	8850
rs113213072	snp	A/G	0.00398564	0.0444627	intron-variant	KAT2B	GRCh38.p7	3:20072680	CTTCTTCCTTTCAAG[A/G]GCTGAGTTGGACTGG	8850
rs113277482	snp	A/C	0.00755907	0.0610114	intron-variant	KAT2B	GRCh38.p7	3:20139513	ATAAGTTTTTGTTGA[A/C]AGATGAGGCAGTGAA	8850
rs113305197	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20113201	CATGTATTTCAGTGT[A/C]TTTTAACTGATGTAA	8850
rs113347043	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20069529	CTTTTCTTTTCTTTT[C/T]TTTTTTTTTTTTTTG	8850
rs113398215	snp	C/T	0.5	0	intron-variant	KAT2B	GRCh38.p7	3:20046418	GAAACCCTGTCTCTA[C/T]AAAAATTACGAAAAT	8850
rs113445746	snp	C/T	0.00795532	0.062565	intron-variant	KAT2B	GRCh38.p7	3:20127772	GTCAGATTAGGGCTA[C/T]GATTTTGGGATGAAA	8850
rs113456299	snp	A/G	0.0236746	0.106192	intron-variant	KAT2B	GRCh38.p7	3:20122376	TACTAACAAACAATA[A/G]CTAGAATCACCCCTT	8850
rs113460994	snp	C/T	0	0	intron-variant	KAT2B	GRCh38.p7	3:20103973	GTATGTAGTTTCTGA[C/T]ACACAGAGCAGGTGC	8850
rs113474040	in-del	-/TATT	0.441295	0.160954	intron-variant	KAT2B	GRCh38.p7	3:20138400	CAATACATTTTTGAC[-/TATT]TAGGTGTTTCTTGTA	8850
rs113478332	snp	A/G	0.00993419	0.0697739	intron-variant	KAT2B	GRCh38.p7	3:20048180	TACAAAGGAAAAAAT[A/G]TTTCATTTGGCAGGC	8850
rs113491905	snp	C/T	0.0178098	0.0926698	intron-variant	KAT2B	GRCh38.p7	3:20074551	GGCTGATGTTGTTCG[C/T]AGTAGTGGTACTATA	8850
rs113513179	snp	A/G	0.5	0	intron-variant	KAT2B	GRCh38.p7	3:20118360	TGTGTGTGTGTGTGT[A/G]TGTGTGTGTATATGT	8850
rs113514169	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20099339	TGCCCTAGATGATGC[A/G]TATGCCGTGCAGCTG	8850
rs113597336	in-del	-/T	0	0	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20136547	CTTTTCATTTGCATC[-/T]TTTTTTTTTCTTCTG	8850
rs113614921	snp	A/G	0	0	intron-variant	KAT2B	GRCh38.p7	3:20110696	AAAAAAAAAAAGAAA[A/G]AAAAAGAAAGAAAAA	8850
rs113664563	snp	C/G	0.5	0	intron-variant	KAT2B	GRCh38.p7	3:20094740	AGTGTGTCTCAATCA[C/G]AAAGGCTGAAGAAAA	8850
rs113688448	snp	C/G	0.5	0	intron-variant	KAT2B	GRCh38.p7	3:20049712	AGGCCATAAAGTAAA[C/G]AAAATAAGCATTCTT	8850
rs113710657	snp	A/G	0.0596104	0.162024	intron-variant	KAT2B	GRCh38.p7	3:20085683	ACCCGGCTATTTTTT[A/G]TGTTTTTAGTAGAGA	8850
rs113718909	snp	C/T	0.0119091	0.0762411	intron-variant	KAT2B	GRCh38.p7	3:20053994	GTAGAGATGGGGTCT[C/T]GCCATGTTGGCAAGG	8850
rs113783668	in-del	-/A	0.167484	0.23599	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038313	GTTCCCTCCCCCAAT[-/A]TGTCACTGTGAAAAT	8850
rs113831913	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20095712	TGCATGTGGCACTAA[C/T]GTAGGCATGAGGGAT	8850
rs113874624	snp	C/T	0.00795532	0.062565	intron-variant	KAT2B	GRCh38.p7	3:20045049	AGACAGGGTCTCGCT[C/T]TGTCACCCTGGCAGG	8850
rs113983972	in-del	-/G	0.5	0	intron-variant	KAT2B	GRCh38.p7	3:20100366	GTAAGTCAAGCAAAA[-/G]AAAGCAAAAAAGAAA	8850
rs114086073	snp	C/G	0.00795532	0.062565	intron-variant	KAT2B	GRCh38.p7	3:20056427	AGTTCTTTGTTGGAG[C/G]TGATACATTAGATAT	8850
rs114109630	snp	A/G	0.0611083	0.163768	intron-variant	KAT2B	GRCh38.p7	3:20051228	AACCCAAACAAAAAA[A/G]ACAAATCAAGGAGGG	8850
rs114158478	snp	A/G	0.00835141	0.0640778	intron-variant	KAT2B	GRCh38.p7	3:20044999	TGTCCCACAGATATT[A/G]ATAGGATTGGGTTAT	8850
rs114217993	snp	C/T	0.00636936	0.0560724	intron-variant	KAT2B	GRCh38.p7	3:20049875	AAGGTGCCAAATGTG[C/T]CAGAAAGTTAAGAAA	8850
rs114222419	snp	A/G	0.0360663	0.129354	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070703	GCAGCCACTCTGACA[A/G]TTTTCTTCAAATTAG	8850
rs114225933	snp	A/G	0.0248432	0.108648	intron-variant	KAT2B	GRCh38.p7	3:20084444	CCTTTGTACAGGGGA[A/G]CCTCTTTCTTCTCTT	8850
rs114238475	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20074818	GGTTCAGGATTTAAA[C/T]ACCCTGTGGAGGAGC	8850
rs114280184	snp	A/G	0.00676609	0.0577691	intron-variant	KAT2B	GRCh38.p7	3:20106571	GGAAGTTAAGAAAAA[A/G]CTGAAAAGTATAAAT	8850
rs114297877	snp	C/G	0.00597247	0.0543191	intron-variant	KAT2B	GRCh38.p7	3:20151670	TTCACCTGTAAAATA[C/G]TACAATTTAAAGCAA	8850
rs114312770	snp	A/G	0.0134861	0.0810011	intron-variant	KAT2B	GRCh38.p7	3:20084307	CTCATTGTTTATTCT[A/G]GGAAGCTTAACCTTT	8850
rs114337756	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20052316	TATCTGTTTTCCTTA[C/T]GACAATAGAAGCTCC	8850
rs114353412	snp	A/G	0.0267878	0.112589	intron-variant	KAT2B	GRCh38.p7	3:20093142	TGAGTTCCCCAAGAA[A/G]CAGACTCTGAGACAA	8850
rs114389142	snp	A/G	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20145337	AGATTTACTAGGAAT[A/G]TACTTTTACTAGTCC	8850
rs114409975	snp	A/G	0.00755907	0.0610114	intron-variant	KAT2B	GRCh38.p7	3:20059284	CAGGCGTGGTGGCAT[A/G]CGTCTAGTAGTCCCA	8850
rs114445546	snp	A/C/T	0.00755907	0.0610114	intron-variant	KAT2B	GRCh38.p7	3:20061718	ATTTGTATTTTCATA[A/C/T]GTATATATGAAAAAA	8850
rs114448070	snp	A/G	0.0162398	0.0886349	intron-variant	KAT2B	GRCh38.p7	3:20045410	GGATGGGGTACACTG[A/G]CACGATCATAGCTCA	8850
rs114448975	snp	C/T	0.00636936	0.0560724	intron-variant	KAT2B	GRCh38.p7	3:20075950	ACGGCTTTATCTCTA[C/T]ACTTTCCCTCCCTTA	8850
rs114491517	snp	C/G	0.0295035	0.117819	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070695	TCAAAGCAGCAGCCA[C/G]TCTGACAATTTTCTT	8850
rs114528005	snp	A/G	0.00029241	0.012088	intron-variant	KAT2B	GRCh38.p7	3:20122664	TTTATTTTGATCATC[A/G]TAGGAGAAAAGAGGA	8850
rs114576770	snp	C/T	0.00993419	0.0697739	intron-variant	KAT2B	GRCh38.p7	3:20047358	ATTACAGGCATGAAC[C/T]ACCACGCCTAGCCTA	8850
rs114613816	snp	A/G	0.00716266	0.059414	intron-variant	KAT2B	GRCh38.p7	3:20051834	TCTTTTCCGTAATTG[A/G]TATATTTAACAAAAT	8850
rs114768196	snp	A/G	0.0256215	0.110247	intron-variant	KAT2B	GRCh38.p7	3:20051246	AAATCAAGGAGGGGT[A/G]CTTGGCCAAGTAGAT	8850
rs114770778	snp	A/G	0.0275645	0.114116	intron-variant	KAT2B	GRCh38.p7	3:20113520	GGAGCTAAAACATCA[A/G]TGCTGCCTTCTTTTC	8850
rs114822418	snp	A/G	0.0352966	0.128072	intron-variant	KAT2B	GRCh38.p7	3:20117612	TCAGTTAGAAGTGCT[A/G]TGGGTTGGTATCTCT	8850
rs114927853	snp	A/G	0.00835141	0.0640778	intron-variant	KAT2B	GRCh38.p7	3:20098865	TGAGGTCCTTGTAAG[A/G]CACAGTTCAGTGGTG	8850
rs115001055	snp	A/G	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20128637	TCTGAATTGACAGAA[A/G]GAGCTCTCATCTATA	8850
rs115003419	snp	A/G	0.029116	0.117091	intron-variant	KAT2B	GRCh38.p7	3:20096102	GTGGTGGAGCCCAGC[A/G]AGCAGAGGGTTGGGT	8850
rs115010922	snp	C/T	0.00716266	0.059414	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20137105	TTTTCTTAATATGTT[C/T]TCAGGTAGCGTTCTT	8850
rs115012799	snp	A/G	0.0271762	0.113356	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070615	GGCCTCTCTTTTCTT[A/G]TACTGTTACACATAT	8850
rs115014362	snp	C/T	0.0331762	0.124449	intron-variant	KAT2B	GRCh38.p7	3:20140412	ACAGGCCAGTCTTAG[C/T]TGGGGTGGGTTGCAT	8850
rs115036994	snp	A/G	0.0150606	0.0854603	intron-variant	KAT2B	GRCh38.p7	3:20083172	GTTTTACATAGCAGC[A/G]ACTTCATATCTTGAG	8850
rs115089796	snp	G/T	0.0123036	0.0774623	intron-variant	KAT2B	GRCh38.p7	3:20052124	ATGTATCTCTGTATC[G/T]TGTTCTCAAAGCCTC	8850
rs115129643	snp	C/T	0.0948562	0.196037	utr-variant-5-prime, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20040068	GCCTCCCAGCGCTGG[C/T]AGACACCGTGAGGCT	8850
rs115176719	snp	A/G	0.0134861	0.0810011	intron-variant	KAT2B	GRCh38.p7	3:20072128	AGATTCCAGCCAGCA[A/G]ACAACAAAAGAAAAC	8850
rs115239756	snp	A/G	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20124976	CTATGGTTGAGTGTA[A/G]GTCAACAGATATTCT	8850
rs115257396	snp	C/T	0.125874	0.217008	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039856	ACTGGTGCAGGCGTG[C/T]GGGGGTCGGATGGGG	8850
rs115260010	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20110757	CCACTGTATGTTGGC[C/T]GAATGCACTTTCTAA	8850
rs115260750	snp	A/G	0.0554779	0.157039	intron-variant	KAT2B	GRCh38.p7	3:20064167	TTTCACATGCCTGAT[A/G]ATTTGTTATTGTCAG	8850
rs115277292	snp	C/T	0.0271762	0.113356	intron-variant	KAT2B	GRCh38.p7	3:20109395	AATCATAGCTCACAG[C/T]AGCCTAGAACTCCTA	8850
rs115453390	snp	A/G	0.02016	0.0983543	intron-variant	KAT2B	GRCh38.p7	3:20062888	GTTGTTGTTGTTGTT[A/G]TTGAGTTGTAGGCAT	8850
rs115456413	snp	C/T	0.0115144	0.0749975	intron-variant	KAT2B	GRCh38.p7	3:20134092	ATGGTGCCTTGAAGA[C/T]GTTTTAAAATTTGAA	8850
rs115495205	snp	A/G	0.0558544	0.157504	intron-variant	KAT2B	GRCh38.p7	3:20087346	ATGTTAATTAAAATG[A/G]GAAAATAATTTATTT	8850
rs115526092	snp	G/T	0.00795532	0.062565	intron-variant	KAT2B	GRCh38.p7	3:20061539	TCCATTTCTAATATT[G/T]TGAGGAACTGTCATA	8850
rs115581195	snp	A/G	0.0314385	0.121371	intron-variant	KAT2B	GRCh38.p7	3:20046206	CACAAAGCATTTATG[A/G]AGAACCCAGTTGCTT	8850
rs115614286	snp	C/T	0.0244538	0.107838	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039214	TTTCAAACGCAGCAC[C/T]GACTTGTATGCTCCA	8850
rs115705944	snp	C/T	0.0123036	0.0774623	intron-variant	KAT2B	GRCh38.p7	3:20051741	TTCATAACAACTGTC[C/T]CTGAAAAGTAGTATT	8850
rs115722607	snp	C/T	0.0107246	0.0724382	intron-variant	KAT2B	GRCh38.p7	3:20122377	ACTAACAAACAATAG[C/T]TAGAATCACCCCTTT	8850
rs115874425	snp	C/T	0.00755907	0.0610114	intron-variant	KAT2B	GRCh38.p7	3:20059851	CTTTTAGAAGATTTC[C/T]ATCACCTCCAAAGGA	8850
rs115880518	snp	A/G	0.00993419	0.0697739	intron-variant	KAT2B	GRCh38.p7	3:20089961	CAGCTTGGACAACAT[A/G]GTGAGAAGCCATCTC	8850
rs115910250	snp	C/T	0.0543475	0.155628	intron-variant	KAT2B	GRCh38.p7	3:20045075	GCAGGAGTACAGTGG[C/T]GTGATCTTGGCTCAC	8850
rs115912731	snp	C/T	0.00914312	0.0669923	intron-variant	KAT2B	GRCh38.p7	3:20083558	AATTCTGGTCAGCAT[C/T]CCCAAAGAGCCAGGA	8850
rs115968804	snp	A/G	0.0640965	0.167152	intron-variant	KAT2B	GRCh38.p7	3:20043210	TGCCTGGCTGAAAGT[A/G]TTCATTTTTATGTAT	8850
rs115988847	snp	C/T	0.0115144	0.0749975	intron-variant	KAT2B	GRCh38.p7	3:20110867	GTCCTCCTCCAGCGT[C/T]GTGCAGTGATGCTGA	8850
rs116034085	snp	C/G	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20093576	TTGTGGTTCAATGGT[C/G]AGCGCATCATGGTCT	8850
rs116035756	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20113597	TTAAATCCTTTTCAC[C/T]GAATATGACAACATT	8850
rs116053912	snp	C/T	0.00755907	0.0610114	intron-variant	KAT2B	GRCh38.p7	3:20065987	AATAACCACAAAATA[C/T]GTGGCTTAAAACAAC	8850
rs116064039	snp	C/T	0.0205511	0.0992634	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039050	TTAAAGCGTCTGGCC[C/T]GAGAGCTATACAGCA	8850
rs116143139	snp	C/G	0.00716266	0.059414	intron-variant	KAT2B	GRCh38.p7	3:20143214	CTTTCATTTGGAAGG[C/G]ATTGATTTTATCGTC	8850
rs116147381	snp	A/G	0.0314385	0.121371	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039811	TGGAAGAGAGTGAAA[A/G]GACAAATGATTGAGA	8850
rs116158633	snp	A/G	0.0115144	0.0749975	intron-variant	KAT2B	GRCh38.p7	3:20092028	TTCATGTGCACTTGA[A/G]AAGAATGTGTATTCT	8850
rs116192285	snp	G/T	0.0267878	0.112589	intron-variant	KAT2B	GRCh38.p7	3:20092432	ACGAGGTTTCACCAT[G/T]TTGGCCCCACTGGTC	8850
rs116193335	snp	C/T	0.0872718	0.189788	intron-variant	KAT2B	GRCh38.p7	3:20122033	GGGTGCCGGTGGGGG[C/T]GGGGTGGAATTAACA	8850
rs116196143	snp	C/T	0.0067357	0.057641	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20140317	TGTGAGCTAAATCCA[C/T]GGATCCCGTACACAG	8850
rs116226235	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20112818	TATTATTCAGATAGT[A/G]TTATTAGATTATGGA	8850
rs116230856	snp	A/G	0.0107246	0.0724382	intron-variant	KAT2B	GRCh38.p7	3:20045941	GCTGTTAACTTGAAA[A/G]TCAAGTAAGAGCAAC	8850
rs116280657	snp	A/G	0.00398564	0.0444627	intron-variant	KAT2B	GRCh38.p7	3:20093580	GGTTCAATGGTGAGC[A/G]CATCATGGTCTCCAG	8850
rs116306076	snp	C/G	0.00597247	0.0543191	intron-variant	KAT2B	GRCh38.p7	3:20124992	GTCAACAGATATTCT[C/G]TGGAAAGAAAACTGT	8850
rs116396223	snp	A/G	0.029116	0.117091	intron-variant	KAT2B	GRCh38.p7	3:20114370	ATCAAGTGAGTTAAT[A/G]TACATCAACCACTTA	8850
rs116396788	snp	A/T	0.0941369	0.195465	intron-variant	KAT2B	GRCh38.p7	3:20118373	GTATGTGTGTGTATA[A/T]GTATATATAAAACTT	8850
rs116476837	snp	A/T	0.00755907	0.0610114	intron-variant	KAT2B	GRCh38.p7	3:20059789	AAGTGTACAATTCAA[A/T]GATTTTTAAGAAATT	8850
rs116477699	snp	A/G	0.0271762	0.113356	intron-variant	KAT2B	GRCh38.p7	3:20090820	GGTCACTGCAACCTC[A/G]ATCTTGTGGGGTGGG	8850
rs116523332	snp	C/T	0.0107246	0.0724382	intron-variant	KAT2B	GRCh38.p7	3:20149703	CATCTATATGCTTTT[C/T]TTTCTCTCTTCTCTC	8850
rs116546565	snp	A/C	0.0535932	0.154675	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038308	ATCTGGGTTCCCTCC[A/C]CCAATTGTCACTGTG	8850
rs116591211	snp	A/G	0.0162398	0.0886349	intron-variant	KAT2B	GRCh38.p7	3:20123964	CAGCTTCCAGGAAAT[A/G]AAGAAATGGCTTGGA	8850
rs116594469	snp	A/G	0.0562307	0.157967	intron-variant	KAT2B	GRCh38.p7	3:20091850	GTCCAAAATAATTGC[A/G]GTTTTTGCCATTGAA	8850
rs116623709	snp	A/G	0.00557542	0.0525036	intron-variant	KAT2B	GRCh38.p7	3:20113989	TGAACTATTTTTAGT[A/G]CTTTTAGTTATTTCT	8850
rs116633408	snp	G/T	0.00597247	0.0543191	intron-variant	KAT2B	GRCh38.p7	3:20108221	TAATGGGAAAACATT[G/T]TACACTGTTTCCATT	8850
rs116699853	snp	C/G	0.00874735	0.0655527	intron-variant	KAT2B	GRCh38.p7	3:20121284	GAGATAGTGAGAATG[C/G]TATGTGGAGAATGTT	8850
rs116730864	snp	A/G	0.0197687	0.0974348	intron-variant	KAT2B	GRCh38.p7	3:20068699	CATGTAGTAGGCCTC[A/G]ATAAATATTGTTGAA	8850
rs116764739	snp	A/G	0.00398564	0.0444627	intron-variant	KAT2B	GRCh38.p7	3:20094501	TTACTAATACCGACC[A/G]CATGGGATTGGGGAT	8850
rs116785376	snp	C/T	0.0205511	0.0992634	intron-variant	KAT2B	GRCh38.p7	3:20148073	CAACTTAAAGAAAAA[C/T]GGCAAACTAATTGTA	8850
rs116786689	snp	C/T	0.00835141	0.0640778	intron-variant	KAT2B	GRCh38.p7	3:20090327	TGAGTGTGATGTTAA[C/T]TGTGGGTTTGTCACA	8850
rs116854133	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20142333	TTTGGAGATCTTAAC[C/T]TAGTTTTTAAAAAAG	8850
rs116860928	snp	C/G	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20063829	TACAGACGTGAGCCA[C/G]CACGCCCGGCCGAGA	8850
rs116936364	snp	C/G	0.0681886	0.171594	intron-variant	KAT2B	GRCh38.p7	3:20081720	GGATTCTTTAATGAT[C/G]AAATTCAGGTGGAGG	8850
rs117118536	snp	A/G	0.0402882	0.136092	intron-variant	KAT2B	GRCh38.p7	3:20079947	GCTCATTTGGTATAA[A/G]TTATGTCTCCCTGAC	8850
rs117322778	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20069399	CTGATAAAGGTCAAG[A/C]GTTGTCTCCAAGATC	8850
rs118005386	snp	A/C/T	0.00835141	0.0640778	intron-variant	KAT2B	GRCh38.p7	3:20049844	AAGATGAAAGAGACA[A/C/T]CTACTCAGGCTATAG	8850
rs118044954	snp	A/G	0.0146672	0.084371	intron-variant	KAT2B	GRCh38.p7	3:20042188	CTATGCTAGTCCACA[A/G]ACCACATTCCAATTC	8850
rs118097078	snp	A/T	0.0115144	0.0749975	intron-variant	KAT2B	GRCh38.p7	3:20081264	TTCACACTGCAGGGC[A/T]TGTGAGGACTGGCTG	8850
rs137884855	snp	A/C	0.000165025	0.00908213	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20119695	CAGTCCTGCCTGCAA[A/C]GCCTCTTCTGGACTT	8850
rs137893912	snp	A/C	0.0158469	0.0875917	intron-variant	KAT2B	GRCh38.p7	3:20045135	TCCTTCCACCTTAGC[A/C]TCCTGAGTAGCTGAG	8850
rs137944428	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20109742	ATAAATGCACTTTAT[A/G]ATTTTTTTCTGCTAC	8850
rs137949377	snp	C/T	0.0569829	0.158885	intron-variant	KAT2B	GRCh38.p7	3:20052599	GTAATCCCAGCACTT[C/T]AGGAGGCTGAGTTGG	8850
rs138000048	snp	A/G	0.0182019	0.0936463	intron-variant	KAT2B	GRCh38.p7	3:20112804	AGAAACTAGATTTTT[A/G]TTATTCAGATAGTGT	8850
rs138067154	snp	C/G	0.00119737	0.0244387	downstream-variant-500B	KAT2B	GRCh38.p7	3:20154559	ATAGGTCATCAGTAA[C/G]AGATTTTCAGGAGAG	8850
rs138099883	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20057685	AGTTTCTAGGCCCCA[A/G]TGTCACCCAGGACCT	8850
rs138112106	snp	C/T	0.0103295	0.0711199	intron-variant	KAT2B	GRCh38.p7	3:20149992	TCTGATGACGTGCAG[C/T]GATAGGTCTAGCAGA	8850
rs138170314	snp	C/G	0.00874735	0.0655527	intron-variant	KAT2B	GRCh38.p7	3:20098661	ATGGTCTTATTTTAA[C/G]TGGGGAAAAAAAGTA	8850
rs138210893	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20088813	ATTCAAAAAATCTTT[A/G]CGAAGACCAATGTCA	8850
rs138218027	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20103532	CATCTATCTCAGCCT[C/T]CTTAGTAGCTGGGAC	8850
rs138228097	snp	A/C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20130419	GTCCAGATGTTTCCA[A/C/G]ATGTTCAAAGTTTAA	8850
rs138261319	snp	A/C	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20083098	CTCTCACTACTGATA[A/C]AGTGTACATTGATGC	8850
rs138266237	snp	A/G	1.64787e-05	0.00287038	missense, intron-variant, nc-transcript-variant	KAT2B	GRCh38.p7	3:20127523	GAGATTGTCTTCTGT[A/G]CTGTAACCTCAAATG	8850
rs138274626	snp	A/G	0.00398564	0.0444627	intron-variant	KAT2B	GRCh38.p7	3:20093919	TAGATGGTTTATCTA[A/G]GGATCCTTTTTCAAG	8850
rs138281729	snp	C/T	0.0115144	0.0749975	intron-variant	KAT2B	GRCh38.p7	3:20060339	GGGCATGGTGGCTCA[C/T]GCCTGTAGTCCCAGT	8850
rs138328807	in-del	-/ACAG			intron-variant	KAT2B	GRCh38.p7	3:20106452	TACACACACACACAC[-/ACAG]ACACACACACACATT	8850
rs138339598	snp	C/T	0.00835141	0.0640778	intron-variant	KAT2B	GRCh38.p7	3:20054093	ATGAGCCATTGTGTC[C/T]GGCTTTAGACTTATT	8850
rs138342880	in-del	-/TTCA	0.00795532	0.062565	intron-variant	KAT2B	GRCh38.p7	3:20066352	ACATCTGCAATGAAC[-/TTCA]CTATTTCCAAATATG	8850
rs138368891	snp	G/T	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20076711	AGTTTCCTACATTTT[G/T]TCTTATCTTATTCAT	8850
rs138379232	snp	A/C/T	0.00011543	0.00759623	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20148278	ACCAGCTTTACAGCA[A/C/T]GCTCAAGAGCATCCT	8850
rs138400645	snp	A/G	0.0252325	0.109451	intron-variant	KAT2B	GRCh38.p7	3:20056113	TGGCTGCTCTGAGAA[A/G]AATAAAGTATATGAG	8850
rs138411087	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038249	TGCCTCCTGAATTCT[A/G]AGGGACGCTTGGGAG	8850
rs138419307	snp	C/G	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20151227	AGGCTTTATTCAAGA[C/G]ATAGGCAGAAGCAGC	8850
rs138511221	snp	A/G	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20120080	AACTCTGCTTCACAT[A/G]TTTCTCATAATTTTC	8850
rs138526983	snp	C/T	0.00636936	0.0560724	intron-variant	KAT2B	GRCh38.p7	3:20110621	GAGGTTGCAGTGAGC[C/T]GAGATTGTACCACTG	8850
rs138544289	snp	C/T	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20050017	CCAGCCTGGGCAACA[C/T]GGTGAGACCCGGTCT	8850
rs138551614	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20124743	TTGTTAAATTTTCAG[C/G]AGTTTTGTGAGCTGG	8850
rs138556636	in-del	-/AAGC	0.00370223	0.042865	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152573	CAAGCAGTGTGCCTA[-/AAGC]AAGGTGGTTTAGTTT	8850
rs138561084	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20113425	TTTTCCCATAACAAA[C/T]TCATTTTGCTTCTTG	8850
rs138608281	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20069209	AACTTGGGCTTATAG[A/G]CTATCTCAGCAAAGA	8850
rs138650015	snp	C/T	1.67444e-05	0.00289343	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20111772	AACGAACTCTAATCC[C/T]CACTCATTTCCCAAA	8850
rs138653461	snp	C/T	0.00636936	0.0560724	intron-variant	KAT2B	GRCh38.p7	3:20094837	ATACCTTTAGGGAGC[C/T]TGGTTTTCTGCATCT	8850
rs138659274	snp	A/G	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20071698	AGTGTTGCTAAAATA[A/G]TGGTGTTCTAGTACA	8850
rs138809710	snp	A/G	0.00795532	0.062565	intron-variant	KAT2B	GRCh38.p7	3:20059818	TTGACAAGTTGTACA[A/G]TCATCACCACAATCT	8850
rs138836969	in-del	-/TCT			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070321	TTCTTTTTTTTTTTT[-/TCT]TTGAGATGGAGTCTC	8850
rs138846321	snp	A/C	0.0150714	0.0855845	intron-variant	KAT2B	GRCh38.p7	3:20134712	AGGATTATAGGCCAC[A/C]GCGCCCAGCCCACTA	8850
rs138879671	snp	A/G	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20050885	TTTGGAAGAACCCAG[A/G]AGGGCAGGAATGTGG	8850
rs138880292	snp	A/C	0.00358779	0.0422022	intron-variant	KAT2B	GRCh38.p7	3:20141656	TAGTTTTTTGTTAGG[A/C]ATTATCTACCTAACA	8850
rs138886225	snp	A/C	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20087433	TAATGTGATATTTTG[A/C]GATGTATATATTATA	8850
rs138887198	snp	C/G	0.00755907	0.0610114	intron-variant	KAT2B	GRCh38.p7	3:20060569	TCACGCCATTGCACT[C/G]CAGCCTGGGCAACAA	8850
rs138890002	snp	C/G	0.00557542	0.0525036	intron-variant	KAT2B	GRCh38.p7	3:20127074	CTTCAGAGACACATA[C/G]CATGTTTGTCCATGA	8850
rs138943712	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20093439	GAGTAGGTTACAGTG[A/G]TAAGAAAAGCCCTTA	8850
rs138945888	snp	C/T	0.00118038	0.0242651	intron-variant	KAT2B	GRCh38.p7	3:20148497	CCATGGGTAATACCA[C/T]TAACATTTTCTAAGT	8850
rs138949460	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20065766	ATATATCAATAGGGT[A/G]TAACTTTAAAGAGTT	8850
rs139068095	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20104396	ACGTCATGTTGATGA[A/G]GAAAGGGAAGTAGAG	8850
rs139072746	in-del	-/TA			intron-variant	KAT2B	GRCh38.p7	3:20121699	ATATAGCTATATATA[-/TA]CATAATATATATGCA	8850
rs139089910	in-del	-/AG			intron-variant	KAT2B	GRCh38.p7	3:20142569	GTAGTTGTCATTAGT[-/AG]AGAGAGAGAGAGAGA	8850
rs139100340	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20061200	TGAATTTGGCTACCA[C/T]AGACACCTTATCTAA	8850
rs139131784	in-del	-/AAA			intron-variant	KAT2B	GRCh38.p7	3:20098322	TATCTTAGTGCTTAC[-/AAA]TGTGGCGCTGGAGTC	8850
rs139143308	snp	C/T	0.00517822	0.0506191	intron-variant	KAT2B	GRCh38.p7	3:20127992	CCGGTCCCTAACAGG[C/T]CACGGACTGGTAATG	8850
rs139147285	snp	C/G	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20052400	AACAGACAAGTTGTA[C/G]TGGGGATTAAATTCC	8850
rs139248240	snp	A/G	0.00874735	0.0655527	intron-variant	KAT2B	GRCh38.p7	3:20121171	AAAATTGTAAAAAAA[A/G]GAACTCGACAAAAGT	8850
rs139282755	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20073387	CCATCATTTCTCTAG[A/G]GCTTCCTGCTTACAA	8850
rs139304351	snp	C/T	0.0248432	0.108648	intron-variant	KAT2B	GRCh38.p7	3:20078193	TCAAAAATAAATAAA[C/T]AAATAAATAAATAAA	8850
rs139361011	snp	C/G/T	0.000115721	0.00760583	missense, synonymous-codon, utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152435	TTGCAAAGAGTACAA[C/G/T]CCCCCTGAGAGTGAA	8850
rs139369417	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038492	TCTCAAAGTACAAAG[A/C]GCACCATTAGAGTTC	8850
rs139385649	snp	A/G	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070337	TTGAGATGGAGTCTC[A/G]CTCTGTACCCAGGCT	8850
rs139426847	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20137335	TGGTTTCTAATAAGA[A/C]ATTCCCAGTCCTGGA	8850
rs139444898	snp	G/T	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20084949	GAGTTAAACCTACTA[G/T]ATGTAGCACCTTAAT	8850
rs139510620	in-del	-/G			intron-variant	KAT2B	GRCh38.p7	3:20129030	AAAAAAAAAAAAAAA[-/G]AATGTTATTCATTTA	8850
rs139524375	snp	A/G	0.00597247	0.0543191	intron-variant	KAT2B	GRCh38.p7	3:20099771	TGTAAGAGAGAGAGA[A/G]AGAGACAGACAGAAA	8850
rs139530682	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20136191	ATATTTGGGTCTGGA[A/C]ACTTGGATTTACTTT	8850
rs139562951	snp	A/T	0.0126979	0.078662	intron-variant	KAT2B	GRCh38.p7	3:20085198	CTATGTCTATTAATT[A/T]AAAAAAAAAGTTTAT	8850
rs139578525	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20051454	GGTTCTGGAAGATGA[C/G]TAGAGTTGCTATACG	8850
rs139598012	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20090124	TCTTTAGGGTTTTCT[A/G]TTTATAAAATTATGT	8850
rs139679499	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20054455	AAAAAGTGTGAATAA[C/T]GTCTCTAATGGTCCA	8850
rs139735292	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039633	TTAAAAAATAGTTTG[A/T]CAGAAAGTATTTAAA	8850
rs139743528	in-del	-/ATATAT/ATATATATAT/ATATATATATATATATAT	0.302686	0.244385	intron-variant	KAT2B	GRCh38.p7	3:20081878	CTCATATATATATAT[lengthTooLong]GTATAAATGTATATA	8850
rs139776907	snp	A/G	0.00398564	0.0444627	intron-variant	KAT2B	GRCh38.p7	3:20105149	CCTCGTCCTCCTAAA[A/G]TGCTGGGATTAAAGG	8850
rs139832420	in-del	-/TC	0.0248432	0.108648	intron-variant	KAT2B	GRCh38.p7	3:20140525	TTTTTTGACACAGAG[-/TC]TCTCTGTCACCTAGA	8850
rs139845144	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20066624	GGCTGGTCTCGAACT[C/G]CTGACCTCATGTGTG	8850
rs139938418	snp	A/G	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20110894	CTGAGGTGCATTTTT[A/G]ACTTTGAGTCTGAGT	8850
rs139957254	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20122034	GGTGCCGGTGGGGGC[A/G]GGGTGGAATTAACAT	8850
rs139991254	snp	C/T	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20127281	AAAAGGATGGTCTAG[C/T]GAGATAGGGGCTACA	8850
rs140018503	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20111470	CTGGCAGGGATATTG[C/T]TGCTTGTTATTGCAG	8850
rs140063664	snp	C/T	0.00199481	0.0315187	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039049	CTTAAAGCGTCTGGC[C/T]TGAGAGCTATACAGC	8850
rs140071012	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20115380	GATGCCTTCTGGAGT[C/T]GCAGTGATCCCAGAA	8850
rs140084056	snp	C/T	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20055959	GTGGTGTTGGATGCA[C/T]TGGTAGTTAATTTCT	8850
rs140118143	in-del	-/G			intron-variant	KAT2B	GRCh38.p7	3:20148161	CAATTTCAGGTTTTT[-/G]TAAGAATGAGCTGAA	8850
rs140157977	snp	C/T	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20063836	GTGAGCCACCACGCC[C/T]GGCCGAGATTCACAA	8850
rs140162853	snp	A/T	0.0193772	0.0965046	intron-variant	KAT2B	GRCh38.p7	3:20044749	TTAGAAATTATCCAA[A/T]TTCATCTGTACTCTT	8850
rs140163286	snp	A/G	0.0456336	0.143994	intron-variant	KAT2B	GRCh38.p7	3:20144388	CTGCCTCCTGGGTTC[A/G]CACCATTCTCCTTCC	8850
rs140187410	in-del	-/AAAC	0.141258	0.225111	intron-variant	KAT2B	GRCh38.p7	3:20145643	AATAATTATTTTACA[-/AAAC]AAACAAAACATCTCT	8850
rs140190605	snp	C/T	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20066743	TTTAACCCACTGCAC[C/T]GCATTAAAAAAAAAA	8850
rs140304073	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20071733	ACCTGGGAAATGTAC[A/G]TGTAAGTAGAAACCC	8850
rs140365734	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20112325	GCGTGATGAACCTCT[A/T]TACTAAATTTCTTGT	8850
rs140420206	snp	C/T	0.00755907	0.0610114	intron-variant	KAT2B	GRCh38.p7	3:20055692	ATGGGGGCCAGATTG[C/T]CAACATATAATTTTT	8850
rs140440561	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20042542	GTTCCACAAAAACCT[A/G]TGAAAAAAAAGAGCA	8850
rs140483462	snp	C/T	0.162909	0.23434	intron-variant	KAT2B	GRCh38.p7	3:20058347	ATAATCTCAGCTACT[C/T]GGGAGGCTGAGGCAG	8850
rs140495714	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20135985	CCTACGTTGGCGGTG[A/T]TCTAGCAGATTGCCT	8850
rs140517174	snp	C/G	0.00358779	0.0422022	intron-variant	KAT2B	GRCh38.p7	3:20064172	CATGCCTGATAATTT[C/G]TTATTGTCAGCTCCT	8850
rs140522055	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20146845	CAGTTCTGATGGCCG[A/G]ACACCTTACTGTTTG	8850
rs140553558	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20129608	CCTGAACTCCTGACC[C/T]CAGGTGATCTGCCCT	8850
rs140635621	snp	C/T	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20093579	TGGTTCAATGGTGAG[C/T]GCATCATGGTCTCCA	8850
rs140653171	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20063567	TTTTTTTTTTTTTGA[A/G]ATGGTTGCTCTGTTG	8850
rs140669287	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20096668	CTTCATTTTTATATG[A/G]CAAAAACAGCTAAAT	8850
rs140696434	snp	C/G	0.00914312	0.0669923	intron-variant	KAT2B	GRCh38.p7	3:20091951	GTTGGTATGATTTCA[C/G]TCTTTTAAAAGTTGT	8850
rs140701103	snp	C/T	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20056071	CCAGTGAATTCAAAT[C/T]AGATTTCCGGTTTGA	8850
rs140709878	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20124601	GGAGATTGCATTTCA[G/T]CATGAGATTTGGAGG	8850
rs140758295	snp	C/G	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20076478	CTTAGTATAACAGCT[C/G]TAGAAAACCTTTTTC	8850
rs140783456	snp	A/C	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20115849	CCTTTTCCAGAATGT[A/C]ATAGGAGTGGAATCA	8850
rs140868981	snp	G/T	0.00835141	0.0640778	intron-variant, utr-variant-5-prime	KAT2B	GRCh38.p7	3:20071603	GATCACTTAAAGAAG[G/T]CTACATCATGTTCAC	8850
rs140914544	snp	G/T	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20072808	CTTTGACCTCAGGGT[G/T]GAAACCTCAACCAAC	8850
rs140951326	snp	C/G	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20113157	TTTGGATGTTGCTCC[C/G]AAAATGGGTTATGAA	8850
rs140972380	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152803	TATTTCATGATAGAT[A/G]ATTAGGGGTTTCCTC	8850
rs140995045	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20043730	GATTTGCTTTTTTTA[A/T]AAAAAAAAAAAATTT	8850
rs140997578	snp	G/T	0.00358779	0.0422022	intron-variant	KAT2B	GRCh38.p7	3:20043668	TGCGTGGCCAAGAGG[G/T]CACTGAGGAGTGCAG	8850
rs141006551	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20102484	CTTAATATCATATCA[A/G]ACATTTCACAGGTTA	8850
rs141010149	snp	A/G	0.000231199	0.0107492	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	KAT2B, MIR3135A	GRCh38.p7	3:20136989	AGAATATCACATAAA[A/G]CATGACATCCTGAAC	8850
rs141019517	snp	A/G	0.158632	0.232706	intron-variant	KAT2B	GRCh38.p7	3:20118336	CCTAAATTTGTGTGT[A/G]TGTGTGTGTGTGTGT	8850
rs141049343	snp	C/G	0.00398564	0.0444627	intron-variant	KAT2B	GRCh38.p7	3:20086902	TTCTCCTGCCTCAGC[C/G]TCCCAAGTAGCTAGG	8850
rs141129248	in-del	-/C	0.324781	0.238553	intron-variant	KAT2B	GRCh38.p7	3:20047074	ATGGTTTTTGTTTTG[-/C]CCCCCCCCTTTTTTT	8850
rs141133935	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20081175	TATTTGAGCAGCCTT[C/T]AAATCCTATTGTGTT	8850
rs141197827	snp	A/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20086309	GAAGAAAAACAAGCT[A/G]TATTGGAGTCTGGGC	8850
rs141225309	snp	C/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20104102	TAATTGAGTGAGTGT[C/G]TAATTATTTGAATAT	8850
rs141311545	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20056217	GGTAGCAGGAATGGA[A/G]GGGTGAGAATTAGTT	8850
rs141323455	snp	C/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20134309	CAAGCTCTTTTAAGG[C/T]CTAGCTTAAACATTT	8850
rs141356365	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	KAT2B, MIR3135A	GRCh38.p7	3:20137858	CAGAAGTTTTCAGCT[C/T]AGGCCAGGTGCAGTG	8850
rs141420598	snp	C/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20057418	TGTCCAAGGAAACAA[C/T]GTATAAGGCACTACT	8850
rs141445570	snp	C/T	0.000115356	0.00759374	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20125996	ACGTGGTTGGCAATT[C/T]CCTCAACCAGAAACC	8850
rs141456670	snp	C/T	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20120793	AGACTTGACGTCAGA[C/T]AAATCTTGGATGTGA	8850
rs141557825	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20103318	CCTGAATGCATTTGC[A/G]ACTTTTAGCAGAGAA	8850
rs141568671	snp	A/G	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20114787	CTGATTGAAGGTTTG[A/G]GACGCTGATGTTAAG	8850
rs141601956	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20069225	CTATCTCAGCAAAGA[C/G]TAGTAAATTTTTAGA	8850
rs141602156	snp	A/G	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070024	GGCCAGGTTCAGCCT[A/G]GCAACAGAGAACTCT	8850
rs141704278	in-del	-/C	0.00438332	0.0466095	intron-variant	KAT2B	GRCh38.p7	3:20050449	TGCCTCCTCCCCACT[-/C]CTGGTAATCCTTATT	8850
rs141705214	snp	C/G	0.00398564	0.0444627	intron-variant	KAT2B	GRCh38.p7	3:20150184	GAAATGTGTGCTGGA[C/G]AAAGTTAAAGCTATA	8850
rs141706147	snp	A/T	0.0115144	0.0749975	intron-variant	KAT2B	GRCh38.p7	3:20066551	TTACAGGCATGTGTC[A/T]CTATGCCTGGCTAAT	8850
rs141809223	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20141568	CTTTTCTCTAACAAA[C/T]AGCTTAGGAGGACAT	8850
rs141840384	snp	C/G	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20093993	TTTGTAGGTGCTTTA[C/G]AATTTGGGTCAAACC	8850
rs141952960	snp	A/T	0.00953873	0.0683987	intron-variant	KAT2B	GRCh38.p7	3:20049662	TCCAATTGAGAGGTA[A/T]GTTCAAAGGATTTTC	8850
rs141960542	snp	A/C	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20084789	GGATGGGTTCTTGAG[A/C]CTTCTAAAAATAGAA	8850
rs141976867	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20135128	GGAGAGAAATAGTTC[A/C]TTTGTGTTTTTATCC	8850
rs142022982	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20087658	CCAGCATCTCTACCC[A/G]TACCTCACGTTCCAA	8850
rs142025762	snp	C/G	0.00914312	0.0669923	intron-variant	KAT2B	GRCh38.p7	3:20128251	ACGCAAACATGTAAT[C/G]ACAATTAGTGACACT	8850
rs142040690	snp	A/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20143984	CCAAACCTCAGCATC[A/G]CACAGTATACCCATA	8850
rs142073414	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20096237	CCTGTTTCTCACTGA[C/T]ACCAGTCACCGATTA	8850
rs142082974	snp	A/G	1.64879e-05	0.00287118	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20101432	GACTGCGATCTCCCA[A/G]TGATGATATTTCTGG	8850
rs142176899	snp	A/G	0.00914312	0.0669923	intron-variant	KAT2B	GRCh38.p7	3:20089562	TGCGCCACCATGCCC[A/G]GCTAATTTTTTTTAT	8850
rs142209125	snp	A/G	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20053223	GTTTCCTCTTCTGCA[A/G]GTTACAATTAAATTC	8850
rs142210659	snp	C/T	0.00358779	0.0422022	intron-variant	KAT2B	GRCh38.p7	3:20051811	TGAACCATCCACTTA[C/T]AAATTAGTCTTTTCC	8850
rs142246987	snp	A/G	0.00636936	0.0560724	intron-variant	KAT2B	GRCh38.p7	3:20111991	TTTGGGTTGACTGCC[A/G]TCATTGCTCCCTTAT	8850
rs142308777	snp	C/T	0.0252325	0.109451	intron-variant	KAT2B	GRCh38.p7	3:20047861	CCTCAAGTGATCTGT[C/T]TGCCTGCGCCTCCTG	8850
rs142313223	snp	A/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20108312	CATTTCAAGTGCTCA[A/G]TAGTTACCAATGGCT	8850
rs142314417	in-del	-/T	0.0554779	0.157039	intron-variant	KAT2B	GRCh38.p7	3:20142866	GGCTATGAGCAAGCA[-/T]AATTGGGTATCTATG	8850
rs142342924	snp	A/G	0.160696	0.233506	intron-variant, nc-transcript-variant	KAT2B, MIR3135A	GRCh38.p7	3:20137638	ACCTCCTGGGCTCAG[A/G]TGATTCTCCCACCTC	8850
rs142346189	snp	A/G	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20111907	ACATTCCAAGGGGAT[A/G]GGAGAAAAGACCCTC	8850
rs142347132	snp	A/G	0.00517822	0.0506191	intron-variant	KAT2B	GRCh38.p7	3:20064807	ATAAATTTTCCATCA[A/G]CGTGTTCTTGCTGTG	8850
rs142416841	snp	C/T	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20063903	TTGTGTGTGTGTTAT[C/T]AGCTAAGGGTCCAGC	8850
rs142430499	in-del	-/G	0.127254	0.217792	intron-variant	KAT2B	GRCh38.p7	3:20134437	GAGTCTCGCTCTGTC[-/G]CCAGGCTGGAGTGCG	8850
rs142439876	snp	C/T	0.00597247	0.0543191	intron-variant	KAT2B	GRCh38.p7	3:20109792	AAAAGACAACATTAA[C/T]ACTTAAGATACCCAT	8850
rs142519488	snp	A/G	0.00557542	0.0525036	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20136340	TGTTGACTACCTTTA[A/G]TTACTTTCTAATGTC	8850
rs142521636	snp	C/G	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20059194	GAGGTGGGCAGATCA[C/G]TTGAGGTCGGGAGTT	8850
rs142548774	snp	A/G/T	0.000214282	0.0103489	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20140325	AAATCCACGGATCCC[A/G/T]TACACAGAATTTTCT	8850
rs142623636	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20132035	AAGATAACATATGAG[A/T]ATTTATTTGAAGCTC	8850
rs142642257	in-del	-/GGCTGGAGTGCAGTGGCGCAGTCTC	0.485664	0.0834419	intron-variant	KAT2B	GRCh38.p7	3:20086825	AGATGGAGTCTCGCA[-/GGCTGGAGTGCAGTGGCGCAGTCTC]GGCTGGAGTGCAGTG	8850
rs142667513	snp	C/T	0.142947	0.22592	intron-variant	KAT2B	GRCh38.p7	3:20128999	GCAATGAGAGCGAAA[C/T]TCCATCTCAAAAAAA	8850
rs142668201	snp	A/G	0.0119091	0.0762411	intron-variant	KAT2B	GRCh38.p7	3:20085113	CTAGCACTTTGGGAG[A/G]CCAAGGTGGGAGGAT	8850
rs142686727	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20117716	TGAAACGTAGATGAA[C/T]GTTCTCTCTGACAAT	8850
rs142765071	snp	C/T	0.00795532	0.062565	intron-variant	KAT2B	GRCh38.p7	3:20051617	ATGTTGGAAAGAGAA[C/T]ATTCAGTCCTGTGTT	8850
rs142783084	snp	C/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20136085	GATCCTTCTGACCTT[C/G]AGGTACTGTGATTCC	8850
rs142787663	snp	G/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20127250	TGCAGGCGACCTAGC[G/T]CTAAAAAGTTCAGAT	8850
rs142805972	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20060895	GGTTGTAATAAACCA[C/T]GATCATGCCACTGCA	8850
rs142817239	snp	G/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20141851	AAGATGTCAGCCTAA[G/T]AGAGAATTCCAAGTA	8850
rs142827794	snp	G/T	0.00517822	0.0506191	intron-variant	KAT2B	GRCh38.p7	3:20054098	CCATTGTGTCCGGCT[G/T]TAGACTTATTTTTTT	8850
rs142840196	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20130604	AGTTGGACACTTTTA[A/G]GGATACTAAAGGGAA	8850
rs142892567	snp	A/T	0.00835141	0.0640778	intron-variant	KAT2B	GRCh38.p7	3:20067671	TTTCTTTATTTATTT[A/T]TTTATATTTTTTTAA	8850
rs142897081	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039397	GCACAATTTTGAAAA[A/C]TACGTAACGTTATAG	8850
rs142898246	snp	A/C	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20152148	TTTTTAAAAAACCCA[A/C]AAAAGAATGAACTTA	8850
rs142946597	snp	C/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20098289	CCCAATGGAAAGCTG[C/T]GTCCTAAAGTTGAAG	8850
rs143077218	snp	A/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20080310	TCCAAAGGTTCTTTG[A/G]ACTTTCTCCCACCTC	8850
rs143093822	in-del	-/AGAT			intron-variant	KAT2B	GRCh38.p7	3:20109284	CTTCCCCTCAGCCCC[-/AGAT]AGATAGATAGATAGA	8850
rs143107074	in-del	-/A	0.00716266	0.059414	intron-variant	KAT2B	GRCh38.p7	3:20111464	CACTAGCTGGCAGGG[-/A]TATTGTTGCTTGTTA	8850
rs143109583	snp	C/T	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20044168	GCTTCAGAGTCATTT[C/T]GGTTCTGTGTTCATT	8850
rs143156951	snp	A/C/G/T	0.00102388	0.022604	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20146376	GTTTACCCTGGACTT[A/C/G/T]CATGTTTTAAAGATG	8850
rs143213363	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20078272	ATCAAAACATAATTG[G/T]AATTTCTATTGTTAT	8850
rs143256707	snp	C/G	0.00478085	0.0486577	intron-variant	KAT2B	GRCh38.p7	3:20098165	AGTCCGGGATGCAGA[C/G]GTTGCCATGAGCTGA	8850
rs143277931	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038502	CAAAGAGCACCATTA[C/G]AGTTCAATGCTTGTG	8850
rs143282162	snp	A/G	0.00835141	0.0640778	intron-variant	KAT2B	GRCh38.p7	3:20082387	TTTAGTAAATTTAAC[A/G]TTAATATAATACCTT	8850
rs143289529	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20056928	ATGATTTGGACTGCA[A/G]TTGCCTTGGAAAGTA	8850
rs143316976	in-del	-/A	0.00755907	0.0610114	intron-variant	KAT2B	GRCh38.p7	3:20055074	AGAGACCCAGCCCAG[-/A]TAGAGGGAACAGAGT	8850
rs143391774	snp	C/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20052954	GCACTCCAGCCTGGG[C/T]GACAAGAGCTAGACT	8850
rs143397346	snp	C/G	0.0115144	0.0749975	intron-variant	KAT2B	GRCh38.p7	3:20122363	CTATATTAGAGAGTA[C/G]TAACAAACAATAGCT	8850
rs143451150	in-del	-/ATT	0.237303	0.249677	intron-variant	KAT2B	GRCh38.p7	3:20129971	ATTATTATTATTATT[-/ATT]TTGAGACAGAGTCTT	8850
rs143461671	snp	C/T	0.0248432	0.108648	intron-variant	KAT2B	GRCh38.p7	3:20075195	CTTGAACCTAGGAGG[C/T]GGAGGTTGTAGTGAG	8850
rs143487608	snp	A/G	0.0150606	0.0854603	intron-variant	KAT2B	GRCh38.p7	3:20049167	GCCTGGCCGGGCATC[A/G]CCTTAACTGCCTAGT	8850
rs143497492	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20123358	CTTAGAAAATTTAGC[C/T]TGGTTACAATATTTT	8850
rs143535597	snp	C/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20109709	AATTTCTATATGAAG[C/T]ACCTTATGAATTACA	8850
rs143548388	snp	A/G/T	4.94966e-05	0.00497456	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20125928	TCTGTCAGCACACTC[A/G/T]GCCAGGGATGAGGCG	8850
rs143552461	in-del	-/AA			intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20135654	GCAAGACTCCATCTC[-/AA]AAAAAAAAAAATAAA	8850
rs143567894	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20066072	ATGTCATCTGGGCCA[C/T]ACTCCTTTTGAAGGC	8850
rs143632609	snp	A/G	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20099650	TGGACATGAAGGCCA[A/G]TTTGGGTTACCTGAT	8850
rs143664817	snp	A/G	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20060026	TGCCGAGTGTAATGT[A/G]TTTGAGATACATCCA	8850
rs143669779	snp	A/T	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20140827	CCTTGATCTGTTTCC[A/T]TTCTCGGTTACCATT	8850
rs143698277	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20103689	GCTGAGATTACATGT[A/G]TGAGTCACTGTGCCC	8850
rs143783310	snp	A/T	0.00597247	0.0543191	intron-variant	KAT2B	GRCh38.p7	3:20134154	ATGCTTTTGCATTTT[A/T]TTTTTTCTTTAAGAA	8850
rs143788373	in-del	-/CGCAGTCTCGGCTGGAGTGCAGTGG			intron-variant	KAT2B	GRCh38.p7	3:20086817	TTTTTTTGAGATGGA[-/CGCAGTCTCGGCTGGAGTGCAGTGG]GTCTCGCAGGCTGGA	8850
rs143856943	snp	A/C/G	0.00531631	0.0512831	intron-variant	KAT2B	GRCh38.p7	3:20072470	CCTAGGTGAGTTCCT[A/C/G]AATCTTCAAGGAAAG	8850
rs143885950	snp	C/T	0.00874735	0.0655527	intron-variant	KAT2B	GRCh38.p7	3:20061568	TACTGTTTTCCATAG[C/T]AGCCATACCATTTTA	8850
rs143894331	snp	A/T	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20151553	ATAAATAGACAAATG[A/T]TAGCGTCTATTCTAA	8850
rs143896251	snp	G/T	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20096492	AACCTGCTACTGAGG[G/T]CATTGTAGATTATGT	8850
rs143909569	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20143815	ATGTTTTCTGTTATA[A/G]GTGGGAGCTGAACAT	8850
rs143961762	snp	A/G	0.0107246	0.0724382	intron-variant	KAT2B	GRCh38.p7	3:20100829	TAGTAAAGAGTTTAA[A/G]TTTTAGTTGTTTAGT	8850
rs144012806	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20120089	TCACATATTTCTCAT[A/G]ATTTTCCTGGGACTA	8850
rs144042517	in-del	-/TG	0.177824	0.239355	intron-variant	KAT2B	GRCh38.p7	3:20114064	AGGGACTTAGGTATC[-/TG]TATTTCTTTTCTCTT	8850
rs144057372	in-del	-/TCA	0.184838	0.241358	intron-variant	KAT2B	GRCh38.p7	3:20104000	GTGCTGGGAAGATGC[-/TCA]TCATCATTTTCCTCC	8850
rs144078126	snp	A/G	0.00993419	0.0697739	intron-variant	KAT2B	GRCh38.p7	3:20124911	GCAAACCACTAGGCA[A/G]ATTAAATAAGATGGG	8850
rs144078165	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20072624	CTGGGAAGGGCTTCT[C/T]GTGAGAGACAAATGC	8850
rs144087112	snp	C/G	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20135859	TAGGAGTAGAACTAA[C/G]GTCAATAAGTAGAAA	8850
rs144143548	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20076783	GGTCTAGGGAATTCT[A/G]TTAGGAATTACGCAA	8850
rs144170558	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20048622	CTCAGATGAATACTC[C/T]GTGTAGTGCCAATAA	8850
rs144181808	snp	A/G	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20121325	AGCAGTGGGATTCAC[A/G]TGTGAGGAAATAAAT	8850
rs144234568	snp	G/T	0.00478085	0.0486577	intron-variant	KAT2B	GRCh38.p7	3:20128501	GTTTTGTTTTGTTTT[G/T]TTTTGTTGCTAATTT	8850
rs144289878	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20055755	CGTTTCAACAAATAC[A/G]TATCAAGACAGAACT	8850
rs144314130	snp	C/T	0.0162398	0.0886349	intron-variant	KAT2B	GRCh38.p7	3:20047208	ACTTGGCCAGGCGCA[C/T]GTCACCATGGCCGGC	8850
rs144316560	in-del	-/A			intron-variant	KAT2B	GRCh38.p7	3:20139235	TCTTTTTTTTTAAAA[-/A]TGTGTTCTTATGTAA	8850
rs144415153	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20102198	TCACGTGACTGTAAT[C/T]CTGGCTACTTGGGAG	8850
rs144429197	snp	C/T	0.00557542	0.0525036	intron-variant	KAT2B	GRCh38.p7	3:20114423	AGAGCTATATATGTG[C/T]GTGACAAATAAAAAT	8850
rs144466502	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20100234	TTGTAAGAAGAACAC[A/G]TGAAATGTGCTTTTT	8850
rs144484975	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20105789	CTGGGTGACAGAGCA[C/T]GACCCTGTCTGAAAA	8850
rs144553523	snp	A/G	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20062727	TCAGCCTCTCAAAGT[A/G]TTGGGATTACAGGCG	8850
rs144592647	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20086846	GAGTGCAGTGGTGCA[A/G]TCTCAGCTCACCACA	8850
rs144602442	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20055146	AGAGTAGTTTAGAAC[A/G]TGGACCTGGGCACCA	8850
rs144610576	snp	C/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20131384	GAGACATCACACTGC[C/T]CAAGATATTTACATT	8850
rs144654473	snp	A/T	0.00597247	0.0543191	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20153016	ATGTGATGTTTGAAG[A/T]CTCTTTATAGACTTT	8850
rs144665869	snp	C/G	0.00914312	0.0669923	intron-variant	KAT2B	GRCh38.p7	3:20113164	GTTGCTCCCAAAATG[C/G]GTTATGAAATTAGGG	8850
rs144695992	snp	C/T	0.0414363	0.137845	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070865	AATACAAAAATTAGC[C/T]GGGTGTGGTGGTGCA	8850
rs144730487	snp	A/G	0.00874735	0.0655527	intron-variant	KAT2B	GRCh38.p7	3:20068823	GGCCTGCCATATTTA[A/G]TTGCTTTGTTGGGGC	8850
rs144738456	snp	A/C	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20127141	GTGCCAGTTCCAGAG[A/C]ACCTCTGCACATACT	8850
rs144760562	snp	C/T	0.0126979	0.078662	intron-variant	KAT2B	GRCh38.p7	3:20072967	ATTGTGTTTATTGAA[C/T]GTTTACTGGTGGTTT	8850
rs144769183	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20111438	GGTAATCTAATTGCA[G/T]TCCCAAGTTTCACTA	8850
rs144772316	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20078569	ATCTTTGGTAGAGAC[A/G]GATTTTGTTATATTG	8850
rs144796121	snp	C/G	0.00795532	0.062565	intron-variant, utr-variant-5-prime	KAT2B	GRCh38.p7	3:20071610	TAAAGAAGGCTACAT[C/G]ATGTTCACTCTTGGC	8850
rs144806388	snp	C/T	5.04511e-05	0.00502225	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20122683	GAGAAAAGAGGAAAA[C/T]GACTGATTCTCATGT	8850
rs144875299	snp	C/T	1.65858e-05	0.00287969	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20122776	TTATGTCTACCATCA[C/T]GGACCCTGCAGCAAT	8850
rs144900083	in-del	-/GT/GTGT			intron-variant	KAT2B	GRCh38.p7	3:20130854	GAATGGATGAGTTTA[-/GT/GTGT]GTGTGTGTGTGTGTG	8850
rs144957599	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20128116	CCAAGGCTTTGTTGG[A/G]CTTTGGGGCGAGGTA	8850
rs144992121	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20079709	CCATATAATTGCCCC[C/T]TCAGTTCCCATTTAT	8850
rs145050585	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20134501	GCAACCTCCGACTCC[C/T]TGGTTCATGCCGTTC	8850
rs145111357	snp	A/C	0.0205511	0.0992634	intron-variant	KAT2B	GRCh38.p7	3:20090902	GTGACACCACACCTG[A/C]CTAATTTTTATTTAT	8850
rs145138566	in-del	-/AT/ATAT/ATATATATATATATATATATATGTATAAATGTATATAGAGAGTCTCAT	0.292981	0.268108	intron-variant	KAT2B	GRCh38.p7	3:20081914	TATATATATATATAT[lengthTooLong]GAGTCTCTACGTATA	8850
rs145176614	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20052443	ATTAAATTCATATCT[C/T]GGGTGGATCATACCT	8850
rs145176889	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20095739	GGATAGAACAGTGGA[C/T]AAAACAGAGTTCTTC	8850
rs145226184	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20147167	AAACAAAATCAAACA[A/G]GCAAAAATTTTCCAG	8850
rs145240236	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20055393	AGAAGCAGACAATAA[A/G]CCAGAAAATAACAGA	8850
rs145259608	snp	A/G	0.0217236	0.101931	intron-variant	KAT2B	GRCh38.p7	3:20097698	TGTGCCGCCATGCCC[A/G]GCTAATATTTGTATT	8850
rs145362785	in-del	-/GG			intron-variant	KAT2B	GRCh38.p7	3:20123426	TCTGCTCCACTGGCT[-/GG]GTTTTTTTCAAATAA	8850
rs145379527	snp	A/G	0.00835141	0.0640778	intron-variant	KAT2B	GRCh38.p7	3:20105849	AAAGAATACATAGCA[A/G]GTTAGCTAGAACTAA	8850
rs145428780	snp	A/T	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20111490	TGTTATTGCAGGCCT[A/T]GTTTTTTTCTGCTAT	8850
rs145442589	snp	C/T	0.00557542	0.0525036	intron-variant	KAT2B	GRCh38.p7	3:20052932	GGTGAGCTGAGATTG[C/T]GCCACTGCACTCCAG	8850
rs145500471	snp	C/T	3.29826e-05	0.00406082	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20101439	ATCTCCCAATGATGA[C/T]ATTTCTGGATACAAA	8850
rs145509731	snp	C/G	0.00636936	0.0560724	intron-variant	KAT2B	GRCh38.p7	3:20115399	GTGATCCCAGAAAGA[C/G]GATCTGAATTCCTGC	8850
rs145622725	snp	A/G	8.243e-05	0.00641936	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20119627	CCTGTGGCTGGGACA[A/G]TTTCATACAATTCAA	8850
rs145660242	in-del	-/TACTACGTTT	0.00953873	0.0683987	intron-variant	KAT2B	GRCh38.p7	3:20061348	CCCTTTGAATGTATA[-/TACTACGTTT]TACTTATTTATTCAT	8850
rs145686216	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20093697	ATCACTTTTTAAATA[C/T]GTATTTTAATCTTTC	8850
rs145700702	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20117274	TTGGCGTGTACACTT[C/T]AGTATTACCTGAAGC	8850
rs145712821	in-del	-/CTTT			intron-variant	KAT2B	GRCh38.p7	3:20139220	CACCCAGCCAGACTT[-/CTTT]CTTTTTTTTTAAAAA	8850
rs145726664	snp	A/G	0.00676609	0.0577691	intron-variant	KAT2B	GRCh38.p7	3:20049741	TTTATTACTGGCCCA[A/G]GACAGACATATACAT	8850
rs145732005	snp	C/T	0.0174175	0.0916809	intron-variant	KAT2B	GRCh38.p7	3:20103126	TTATATCTTCATTTC[C/T]GTATCTTTCATTTTA	8850
rs145744142	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20097208	TCTTGGAACTGTGCT[C/T]CCTGGCAGCTCCCCA	8850
rs145780391	in-del	-/AAGG	0.00716266	0.059414			GRCh38.p7	3:20149545	TGTTAAAAATGTGAA[-/AAGG]AAGAGTGAAAGGGAC	8850
rs145812230	snp	C/G	0.00636936	0.0560724	intron-variant	KAT2B	GRCh38.p7	3:20056092	TCCGGTTTGAAGTGA[C/G]CCCTCTGGCTGCTCT	8850
rs145828732	snp	A/G	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20067138	CAGTCATTATGAACA[A/G]AAGAAATAAAAATAT	8850
rs145866875	snp	C/T	0.0111196	0.0737302	intron-variant	KAT2B	GRCh38.p7	3:20056057	CATCTGGGCTGTTTC[C/T]AGTGAATTCAAATTA	8850
rs145877913	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20133383	AAATTAAAATGAATA[G/T]TTACATCCTTGGTTA	8850
rs145879932	in-del	-/A			intron-variant	KAT2B	GRCh38.p7	3:20107360	CCAATATATAAAAAA[-/A]TGCCATTTCAGCTGG	8850
rs145929107	snp	A/T	0.00557542	0.0525036	intron-variant	KAT2B	GRCh38.p7	3:20105038	TTACAAGTGCGTGCC[A/T]CCATGCCTGGCTAAT	8850
rs145947449	snp	A/C	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20109843	CAACATTTGGGTGTA[A/C]ATTATTAAAGGAAAA	8850
rs145965717	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20066561	GTGTCACTATGCCTG[C/G]CTAATTTTTGTGTTT	8850
rs146049966	snp	C/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20127263	GCTCTAAAAAGTTCA[C/G]ATAAAAGGATGGTCT	8850
rs146051095	snp	C/G	0.00517822	0.0506191	intron-variant	KAT2B	GRCh38.p7	3:20051676	ATGCCACCCTCTCCC[C/G]AGGAATGACAGTGAG	8850
rs146070285	snp	C/T	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20130769	AGAAAAGCAATCACT[C/T]CTTGTAAGTGACTTG	8850
rs146070491	snp	A/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20054367	TTCCTGACCTCGTGA[A/T]CCACCCTCATCGGCC	8850
rs146177661	snp	G/T	0.00597247	0.0543191	intron-variant	KAT2B	GRCh38.p7	3:20151338	TGTACGTACATTTAC[G/T]TACCTTATTAAATGA	8850
rs146273319	snp	C/T	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20064808	TAAATTTTCCATCAA[C/T]GTGTTCTTGCTGTGG	8850
rs146291968	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20084948	TGAGTTAAACCTACT[A/G]TATGTAGCACCTTAA	8850
rs146313402	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20148148	TCTGGAATGGTTCCA[A/G]TTTCAGGTTTTTGTA	8850
rs146329886	snp	C/G	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20051282	TAAGGAATATGAAAG[C/G]AAGAGAGGTAGAATG	8850
rs146376210	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20151614	CAGTGAGGATTGAAG[A/G]AACCCTACTTTAGTT	8850
rs146392085	snp	C/T	0.0414363	0.137845	intron-variant	KAT2B	GRCh38.p7	3:20068099	CCTCCCGGGTTCAAG[C/T]GATTCTGCTGCCTCA	8850
rs146487562	in-del	-/AAC	0.215723	0.247639	intron-variant	KAT2B	GRCh38.p7	3:20060943	GAGACCCTGTCTCAA[-/AAC]AACAACAACAACAAC	8850
rs146498981	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20118073	TATTACCCTTTCTCT[A/G]TCCCTTCTTTTTCTC	8850
rs146499925	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20043192	TATAGGCATGGGCCA[A/C]CATGCCTGGCTGAAA	8850
rs146518387	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20122003	ATGCAAACTGATTTC[C/T]GTACATATATGGTGG	8850
rs146573717	in-del	-/ACAC	0.259951	0.249802	intron-variant	KAT2B	GRCh38.p7	3:20060617	AAAACAAACAAACAA[-/ACAC]ACAAACAACAAACTG	8850
rs146619713	snp	A/G	0.0123036	0.0774623	intron-variant	KAT2B	GRCh38.p7	3:20059654	AGCTTGCGGTGAGCC[A/G]AGATCGTACCACTGC	8850
rs146637369	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20144173	GCCATCTGTAGGTCA[C/T]TGCATTTGAGAGTCC	8850
rs146639164	snp	C/T	0.030278	0.119257	intron-variant	KAT2B	GRCh38.p7	3:20063703	GTGAGCCACCATGCC[C/T]GGTTAATTTTTGTAT	8850
rs146710195	in-del	-/TTTTG	0.102726	0.202016	intron-variant	KAT2B	GRCh38.p7	3:20128482	TGTGTTGGAGTGTCT[-/TTTTG]TTTTGTTTTGTTTTT	8850
rs146721823	snp	C/G	0.000284193	0.011917	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20122692	GGAAAATGACTGATT[C/G]TCATGTTCTGGAGGA	8850
rs146740276	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20075632	GAACTCAAGGAAACA[C/T]TTCAGTTTACTGGTT	8850
rs146778958	snp	C/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20042011	TATCCTACACTGGTT[C/T]AATAAATATTTGTTG	8850
rs146782368	in-del	-/TTTTC	0.428333	0.175206	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20069510	GCAGAGAGCTTTTCT[-/TTTTC]TTTTCTTTTCTTTTC	8850
rs146827414	snp	A/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20126553	CTAGGCCGGGCATGG[A/T]GGCTCATGCCTGTAA	8850
rs146859579	snp	C/G	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20096556	CAAAACAAAAGCACT[C/G]AGAGCTTATGGGTAG	8850
rs146878313	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20102132	ACCAGCCTGGCCAAT[A/C]TGGTGAAACCCCATC	8850
rs146900802	snp	A/G	0.00835141	0.0640778	intron-variant	KAT2B	GRCh38.p7	3:20077373	AAGAAAAGAATTCTA[A/G]CTTGGCCCTGCAGTT	8850
rs146901361	snp	C/T	0.00795532	0.062565	intron-variant	KAT2B	GRCh38.p7	3:20129524	GGAACTATAGGCACA[C/T]GCCACCATGCCCGGC	8850
rs146918118	snp	C/T	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20082292	CGCCCTCCTCAGCCT[C/T]CCAGAGTGTTGGGAT	8850
rs146935516	snp	G/T	0.00438332	0.0466095	intron-variant	KAT2B	GRCh38.p7	3:20086694	CCTTTCAATTACTTT[G/T]CTGTATTAGAAATGA	8850
rs146991175	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20149707	TATATGCTTTTCTTT[C/G]TCTCTTCTCTCTGAC	8850
rs147008268	snp	A/G	0.000798403	0.0199641	downstream-variant-500B	KAT2B	GRCh38.p7	3:20154478	GGTTGATAACCATCA[A/G]TTGAATCCTTAAACC	8850
rs147008372	snp	C/G	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20098402	TTTGGGCAAGTTAAT[C/G]TGCCTTGTTAGTAGT	8850
rs147024080	snp	A/G	0.0182019	0.0936463	intron-variant	KAT2B	GRCh38.p7	3:20103463	ATCCTGGGCTGGAGC[A/G]CAGTGGCATGATCAT	8850
rs147116092	snp	A/G	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20119905	TGCTATCTTAAAACT[A/G]TAATAACTTATTGTC	8850
rs147168994	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20095858	ACAAAGTAGGATAAG[C/T]GGAATCAGAATGGCA	8850
rs147185601	snp	A/C	0.0119091	0.0762411	intron-variant	KAT2B	GRCh38.p7	3:20099734	GAATATGGTAACTTC[A/C]TTTAAAGGCTGTGTG	8850
rs147209233	in-del	-/TTG	0.0410537	0.137264	intron-variant	KAT2B	GRCh38.p7	3:20089842	TTTTGTTTTGATAGT[-/TTG]TTGTTAGTATACAGA	8850
rs147272751	snp	G/T	0.0162398	0.0886349	intron-variant	KAT2B	GRCh38.p7	3:20115636	AAATTGAAGTATAAT[G/T]TATATATAGTAAAAT	8850
rs147304960	snp	A/G	1.64866e-05	0.00287106	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20119636	GGGACAATTTCATAC[A/G]ATTCAACCTCATCTT	8850
rs147379111	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20136146	TCTTTAGAAAAATGT[G/T]CCACCAAATTGCAGA	8850
rs147396149	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20143574	TCTTACAAAAAGATA[C/T]ATGTGCTTTTATGTT	8850
rs147396246	snp	A/G	0.00795532	0.062565	intron-variant	KAT2B	GRCh38.p7	3:20089692	AGTGTGAGCCACTGC[A/G]CCTGGCCTACTTTCT	8850
rs147457444	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20086842	GCTGGAGTGCAGTGG[C/T]GCAATCTCAGCTCAC	8850
rs147518139	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20115128	GGCTATTTTCAAACC[C/T]AATTATAGTCTCAGT	8850
rs147520060	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038953	TCCCAATGTTTATAT[A/G]TTAACCTGCATTACA	8850
rs147558849	snp	A/C	0.00557542	0.0525036	intron-variant	KAT2B	GRCh38.p7	3:20086743	CTCTCTAATTTTAAG[A/C]CCTTTAAACTGTCTT	8850
rs147575538	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20091747	TAAGTTCTTCTCTGA[A/C]CCATTGGTTGTTCAG	8850
rs147591721	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20052444	TTAAATTCATATCTC[A/G]GGTGGATCATACCTT	8850
rs147607816	snp	C/T	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20055586	CCAGAAGTGGCTTGT[C/T]GTGTGTGAGGCCTGT	8850
rs147670134	in-del	-/TATAT			intron-variant	KAT2B	GRCh38.p7	3:20062310	TATATAAAATATAAT[-/TATAT]ATATATAAAATATTT	8850
rs147677527	snp	C/G	0.00204416	0.0319109	intron-variant	KAT2B	GRCh38.p7	3:20111554	TTCTGATGACCTGGG[C/G]GTTTATGGGATATTG	8850
rs147679842	snp	C/T	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20064646	GGTAGAATGAGTAAC[C/T]CCAGGCAAGTCTCTT	8850
rs147694086	snp	C/T	0.0955749	0.196603	intron-variant	KAT2B	GRCh38.p7	3:20067746	GTGGTGCGATCTTGG[C/T]TCACTGCAACCTCTG	8850
rs147708206	snp	A/G	1.64912e-05	0.00287147	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20101384	TCCTAAACCGCATCA[A/G]CTATTGGCATCTGGA	8850
rs147765751	snp	G/T	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20128662	TCTATACCTTGTCCT[G/T]TTCTACTTTCTTGCT	8850
rs147798143	snp	G/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20085995	GCTGTTTTGAGCTGG[G/T]CATGGTGGCTCACAC	8850
rs147806208	in-del	-/TTC	0.0248432	0.108648	intron-variant	KAT2B	GRCh38.p7	3:20080078	CTGCAGCTTCTGGAG[-/TTC]TTATTTCCATTCCTG	8850
rs147870914	snp	A/T	0.00438332	0.0466095	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20153674	CCTGATTACACTACA[A/T]AGAAAAGTGAGACAT	8850
rs148013157	snp	A/G	0.0146672	0.084371	intron-variant	KAT2B	GRCh38.p7	3:20075991	AGATTGATGGGTGGG[A/G]TTGAAGGTTCCAATC	8850
rs148027576	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20066076	CATCTGGGCCACACT[C/T]CTTTTGAAGGCTGTA	8850
rs148085980	snp	A/C	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20141190	ATAGACATTTACCTT[A/C]CTGTATATTAATCTC	8850
rs148135073	snp	C/T	0.00874735	0.0655527	intron-variant	KAT2B	GRCh38.p7	3:20134290	TCTCTTGTTTTCAAT[C/T]TGACAAGCTCTTTTA	8850
rs148170754	snp	A/C/T	6.63509e-05	0.00575951	intron-variant	KAT2B	GRCh38.p7	3:20072505	ACGAGTTCATTGTAG[A/C/T]GTGAGACTCTTAACT	8850
rs148208028	in-del	-/TT			intron-variant	KAT2B	GRCh38.p7	3:20131031	TTTAGTTTCCTGGCC[-/TT]TTTTTTTTTTTTTTT	8850
rs148220473	snp	C/G	0.00438332	0.0466095	intron-variant	KAT2B	GRCh38.p7	3:20044398	CTCCAGCCTGGGTGA[C/G]AGAGCAAGATTCTCC	8850
rs148245439	snp	G/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20104054	CTCAGTCACTGCCAA[G/T]GTGGAGCTTATTAAG	8850
rs148293867	snp	A/T	0.00557542	0.0525036	intron-variant	KAT2B	GRCh38.p7	3:20098195	AGATCATGCCACTGC[A/T]CTCCAACCTGGCCGA	8850
rs148310305	snp	C/G	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20057349	GGTTGGGCTGGTTAT[C/G]TGGATGTGAGAGTCA	8850
rs148381416	snp	C/T	0.00716266	0.059414	intron-variant	KAT2B	GRCh38.p7	3:20114620	AAGATTAATGCATTT[C/T]TACTGATGTAATTCA	8850
rs148400162	snp	C/G	0.00597247	0.0543191	intron-variant	KAT2B	GRCh38.p7	3:20100659	AATTTTATTTTGCCT[C/G]CAAACTCTATTAAAT	8850
rs148416530	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20059069	AAGAGAAAACTTCTG[C/G]CAATCCCAGCTGCTT	8850
rs148471575	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20055389	TAGCAGAAGCAGACA[A/G]TAAGCCAGAAAATAA	8850
rs148473980	snp	C/T	0.0130921	0.0798413	intron-variant	KAT2B	GRCh38.p7	3:20131636	GCAGTGGCATGATCA[C/T]AGCTCCCTGCGTCTG	8850
rs148488983	snp	A/G	0.0123036	0.0774623	intron-variant	KAT2B	GRCh38.p7	3:20117691	CTTGTTGACTGAACT[A/G]TGGCTGTGTTGAAAC	8850
rs148507695	in-del	-/C	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20085003	ATCTGAAGGAATTTA[-/C]TTGATATTGTATACT	8850
rs148522136	snp	A/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20127166	CATACTCTGTTCTCT[A/G]TTTGTAAACCTCAGG	8850
rs148538708	snp	A/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20078599	GCCTGGGCTGGTCTC[A/T]AACTCCTGAGGTCAA	8850
rs148559438	snp	G/T	0.00636936	0.0560724	intron-variant	KAT2B	GRCh38.p7	3:20067159	ATAAAAATATACTTT[G/T]TACTGGGATCCCAAG	8850
rs148559450	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20075907	GCGAGACTCCCATCT[A/C]AAAAAAAAAAAAAAA	8850
rs148562347	snp	A/G	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20151993	GAGCCTCTTCTGTAT[A/G]ATTCTGACTGAATAG	8850
rs148599940	in-del	-/A	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20100327	TATTGAGGTGAGGGG[-/A]TTTAGTAGCAATGTG	8850
rs148610011	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20143830	AGTGGGAGCTGAACA[C/T]TGGGGATATATGCTC	8850
rs148625837	snp	C/T	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20096101	CGTGGTGGAGCCCAG[C/T]GAGCAGAGGGTTGGG	8850
rs148694038	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20051773	AATATATGATGAGCT[C/T]GTTATTTAATGGCTG	8850
rs148725281	snp	A/G	1.65034e-05	0.00287253	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20101358	AACAATAGTTGAGTT[A/G]GCAAAAATGTTCCTA	8850
rs148749713	snp	A/G	0.0263992	0.111815	intron-variant	KAT2B	GRCh38.p7	3:20047221	CACGTCACCATGGCC[A/G]GCTAATTTTTGTATT	8850
rs148752835	snp	C/T	0.0240643	0.107019	intron-variant	KAT2B	GRCh38.p7	3:20120375	TGGGATTACAGGTGC[C/T]CACCATCATGCCCTG	8850
rs148768607	snp	A/G/T	0.0047834	0.0487097	intron-variant	KAT2B	GRCh38.p7	3:20106360	GGAATACATGTGCTC[A/G/T]TGCACGTCCGTTTCC	8850
rs148858343	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20123075	AAAAATTTCAAGCCC[G/T]CATAAATGTTGCAGA	8850
rs148948317	snp	G/T	0.00557542	0.0525036	intron-variant	KAT2B	GRCh38.p7	3:20059945	CTGTCTCTATAAATT[G/T]GCCTTTTCTGGATGG	8850
rs148960024	snp	A/C	0.0152058	0.0858585	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20147980	GAGACAGGCTGGAAA[A/C]CGAGTGGAAAAGAGA	8850
rs148998269	snp	A/G	0.00597247	0.0543191	intron-variant	KAT2B	GRCh38.p7	3:20133792	ACCATTGCTGGCACT[A/G]GGTACATAAACTGTA	8850
rs149121653	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20074987	ATAATACCATAAGGC[C/T]GGGCGTGGTGGCTCA	8850
rs149128893	in-del	-/A			intron-variant	KAT2B	GRCh38.p7	3:20110371	TCACTTCTGGGAGAT[-/A]AAAAAAAAAATAGGG	8850
rs149138881	snp	A/G	8.57905e-05	0.00654889	intron-variant	KAT2B	GRCh38.p7	3:20148023	GACGGGCAAGAGGAT[A/G]TTAATGGAAGTGATT	8850
rs149155259	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20098155	GAATTGCTTGAGTCC[A/G]GGATGCAGAGGTTGC	8850
rs149170272	in-del	-/T	0.00636936	0.0560724	intron-variant	KAT2B	GRCh38.p7	3:20151920	AATGCAGTCTGATTG[-/T]TTTAAGTAATTAAAT	8850
rs149247089	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038361	AGTTGAAAGAATTGC[A/G]CACTGTGCCCATTAC	8850
rs149248564	snp	C/T	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20151329	TGGGGATATTGTACG[C/T]ACATTTACTTACCTT	8850
rs149277090	in-del	-/AAT			intron-variant	KAT2B	GRCh38.p7	3:20073723	CTTTTTAAAAAAATA[-/AAT]AAATAAAACAGAACG	8850
rs149314722	snp	A/G	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20065793	AGTTAGGACCACTTA[A/G]GGATGCTGAGACTAT	8850
rs149320266	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20095175	GGATTGATGGTAAGA[C/T]TGATGAAAGAGGACC	8850
rs149337134	snp	G/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20054737	CTGACAAGCTGGTGT[G/T]GAAACTAGATGGCAG	8850
rs149387593	snp	A/T	0.0130921	0.0798413	intron-variant	KAT2B	GRCh38.p7	3:20127098	TCCATGACTTCCTGC[A/T]CTCCCTGACCCCTCC	8850
rs149389663	snp	A/G	0.00716266	0.059414	intron-variant	KAT2B	GRCh38.p7	3:20051064	AATTAGCTGGGCATG[A/G]TGGCACACACCTGTA	8850
rs149478456	snp	A/G	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20143707	TTATGCAGCCATAAA[A/G]AAGAACAAAATCATG	8850
rs149479405	snp	A/G	0.00517822	0.0506191	intron-variant	KAT2B	GRCh38.p7	3:20061534	GTAATTCCATTTCTA[A/G]TATTTTGAGGAACTG	8850
rs149513220	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20068300	TGTGCTTGACCCTGT[C/G]TGGTTTAATTTCAAC	8850
rs149530028	snp	C/T	0.0111196	0.0737302	intron-variant	KAT2B	GRCh38.p7	3:20135480	TAACACAGTGAAACC[C/T]CGTCTCTACTAAAAA	8850
rs149547090	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20089043	CAGTTGACTGTAAAT[A/G]GATAGATTTCTGGGC	8850
rs149611433	snp	A/G	0.000249441	0.011165	missense, utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152491	AGAAATTCTTCTTCA[A/G]TAAAATTAAGGAAGC	8850
rs149617489	snp	C/G	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20046957	ACAGGACAACTCCCC[C/G]CAACGAATGATTATC	8850
rs149656091	snp	A/G	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20092100	CATTTTCTTTAAAGT[A/G]TAGTTCAAGCCCAGT	8850
rs149724448	snp	C/T	0.0827057	0.186409	intron-variant	KAT2B	GRCh38.p7	3:20048910	GGAGTCTTGCTCTGT[C/T]GCCAGGCTGGAGTGC	8850
rs149773039	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20040992	AGAAGGGGGATCACT[A/G]AGACGGAGAGCCCTT	8850
rs149776064	snp	C/T	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20117013	AACAGTTTCCTCCCT[C/T]AGGCAGTGGGGGACC	8850
rs149847693	snp	C/T	0.00835141	0.0640778	intron-variant	KAT2B	GRCh38.p7	3:20066835	AAAATATTATTATAA[C/T]ATGTAATCAATATAA	8850
rs149866194	snp	A/G	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20133320	TCCTAGAGACCTTTC[A/G]GCTTTAGTGCATATA	8850
rs149867259	snp	C/G	0.00398564	0.0444627	intron-variant	KAT2B	GRCh38.p7	3:20056024	TACTAGTTTGTTTAT[C/G]TGTTGACTTGTTATG	8850
rs149881135	snp	C/T	0.000710339	0.0188325	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20122756	GATGGAATTAATCAA[C/T]GAGGTTATGTCTACC	8850
rs149918250	snp	C/T	0.00358779	0.0422022	intron-variant	KAT2B	GRCh38.p7	3:20128036	GGACCTCTGTCTCAC[C/T]GTGAGTGTATGTGTA	8850
rs149934969	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20079483	TGCTGGGATTACAGG[C/T]GTGAGCCACCGCTTC	8850
rs149949115	in-del	-/AG			intron-variant	KAT2B	GRCh38.p7	3:20099760	GTGTGTGTGTGTGTA[-/AG]AGAGAGAGAGAGAGA	8850
rs149961286	in-del	-/TC	0.0626037	0.165477	intron-variant	KAT2B	GRCh38.p7	3:20049078	TGTTGCCCAAGATGG[-/TC]TCGATTTCTTGACCT	8850
rs149989566	snp	A/C/G	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20074550	TGGCTGATGTTGTTC[A/C/G]TAGTAGTGGTACTAT	8850
rs150041206	snp	A/G	0.267636	0.249377	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070462	GGCGCCTGCCACCAC[A/G]CCCGGCTAATTTTTT	8850
rs150042375	in-del	-/G	0.0111196	0.0737302	intron-variant	KAT2B	GRCh38.p7	3:20131661	CGTCTGCGACCTCCT[-/G]TGCTCAGGTAATCCT	8850
rs150061672	snp	A/G	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20137415	GGAAGGCCTCCATTT[A/G]TGACAGCAGAAAGGA	8850
rs150096934	snp	C/T	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20076524	TTCCTCCCTCCTTTC[C/T]GTGCTTTTTGAAAAA	8850
rs150164221	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20108596	CATTATGTTACAGTC[A/G]TTTGTAGTATTCAGT	8850
rs150169098	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20141599	CTGTCTTATACCCAT[A/C]TTTGTTTTCTGGTTT	8850
rs150204618	in-del	-/AC	0.00795532	0.062565	intron-variant	KAT2B	GRCh38.p7	3:20120157	AGGGCAGGAAGAAAT[-/AC]ACAGTCTCTTGAAGC	8850
rs150218994	snp	C/T	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20103004	ACACCCTTTTCCTCT[C/T]TTTCTCTTCACTTTT	8850
rs150225406	in-del	-/TCTTT			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20069518	CTTTTCTTTTTCTTT[-/TCTTT]TCTTTTCTTTTTTTT	8850
rs150233391	snp	A/G	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20087422	TTTATCGTGTATAAT[A/G]TGATATTTTGAGATG	8850
rs150235546	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20059792	TGTACAATTCAATGA[C/T]TTTTAAGAAATTGAC	8850
rs150249316	snp	A/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20050394	ACTGCCACCTAGATA[A/T]AGCTGTAGGACATTT	8850
rs150300470	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20044997	GGTGTCCCACAGATA[C/T]TGATAGGATTGGGTT	8850
rs150306830	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20119144	TTTCCTTTTTAATCA[A/G]AAAAATACTTTTGTG	8850
rs150351875	snp	A/C	0.0001157	0.00760503	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20146393	ATGTTTTAAAGATGG[A/C]GTTCGACAGATTCCT	8850
rs150358826	snp	A/C/T	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20112519	AAAATTTAAGCTAAG[A/C/T]GGTTGGATGCTGGTG	8850
rs150423426	snp	G/T	0.00438332	0.0466095	intron-variant	KAT2B	GRCh38.p7	3:20064340	ATCACTTGTCATTTC[G/T]TTGTGATGAGAACAT	8850
rs150426554	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20146852	GATGGCCGAACACCT[C/T]ACTGTTTGCACCATG	8850
rs150448813	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20129947	TAACAGCTTCACTCT[C/G]TGGTCACAGTACCCA	8850
rs150466082	snp	A/T	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20082583	TTGTTGACTTTTATA[A/T]CATTGACATTTTGAT	8850
rs150512785	in-del	-/GAA			intron-variant	KAT2B	GRCh38.p7	3:20124869	GGGCCTTCCTTCCTT[-/GAA]GAGCTGTTTGTGGAG	8850
rs150539065	snp	G/T	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20150210	CTATAAATGGTGTTC[G/T]TCAGTAGGGCAGTAT	8850
rs150557507	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20132042	CATATGAGAATTTAT[C/T]TGAAGCTCCTCTCCT	8850
rs150578715	in-del	-/A	0.0562307	0.157967	intron-variant	KAT2B	GRCh38.p7	3:20110251	CTGCTCTGAAGGAAT[-/A]AAGAATCTGTGGAAT	8850
rs150607105	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20094461	ACCATATCAGAGCCT[C/T]AGTTTCCTCAATTGT	8850
rs150623078	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20078845	AGACCCCTCACCCTA[C/T]AACCAGAATTGATTC	8850
rs150639025	snp	A/T	0.00438332	0.0466095	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039495	TTTGACAATGCTTTT[A/T]AGACAATCTTTCTTT	8850
rs150650600	snp	A/G	0.000428661	0.0146338	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20119600	TTTGCCGGGGCAGTT[A/G]TCAATCCACCTCCTG	8850
rs150747561	snp	C/T	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20104195	CTCCTGAGCCAACAG[C/T]TGAAGGCAAAAAGTG	8850
rs150763956	snp	A/G/T	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20061066	CATTATTGTGCAATC[A/G/T]TCACCACCATTCATC	8850
rs150815003	snp	C/G	0.0103295	0.0711199	intron-variant	KAT2B	GRCh38.p7	3:20135394	GCGCGGTGGCTCACG[C/G]CTGTAATCCCAGCAC	8850
rs150836867	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20121105	GAATTTGAGGACTTA[C/T]TGGTCAGATGTCTGA	8850
rs150853153	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20073079	GGCCTGTGCTAGTAT[A/G]TTGTTCTTTGTCCTA	8850
rs150884035	snp	C/T	0.000430008	0.0146567	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152456	TGAGAGTGAATACTA[C/T]AAATGTGCCAATATC	8850
rs150902545	snp	C/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070084	TAGACAAAAGACGGT[C/T]ACTTGAGCTACTCAC	8850
rs150927279	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20136817	TATATTTCATTCAGG[A/G]AAGGTCCTGGTTGGT	8850
rs150927386	in-del	-/GTT	0.00993419	0.0697739	intron-variant	KAT2B	GRCh38.p7	3:20091583	GAGGTGTAACATTAG[-/GTT]GTTCATTTGAGATCT	8850
rs150946412	snp	G/T	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20123680	GGATTGTGCATTGCA[G/T]TTAATTCTTATCTCT	8850
rs150952531	snp	A/G	3.30524e-05	0.00406511	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20146335	TTAAAAAACTGATTG[A/G]AAGAAAACAGGCACA	8850
rs151011429	snp	C/T	0.0115144	0.0749975	intron-variant, utr-variant-5-prime	KAT2B	GRCh38.p7	3:20071506	TGAACCTTTCATACG[C/T]TGAGACCTGCTGAAG	8850
rs151068697	snp	C/G	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20152248	TAATCAAACCAACAA[C/G]ATAGATTCCTTTCCC	8850
rs151085224	snp	A/C	0.0240643	0.107019	intron-variant	KAT2B	GRCh38.p7	3:20102262	CAGAGTTTGCAGTGA[A/C]CTGAGATCGTGCACT	8850
rs151134356	snp	A/G	0.00557542	0.0525036	intron-variant	KAT2B	GRCh38.p7	3:20096268	CTGCTGCCATTCCCC[A/G]TAGCTGCCTCTTCAC	8850
rs151150770	snp	A/G	0.0111196	0.0737302	intron-variant	KAT2B	GRCh38.p7	3:20055882	ATTTAGCTATTTTTC[A/G]TATAAATGTTACCAC	8850
rs151153098	snp	A/G	0.00478085	0.0486577	intron-variant	KAT2B	GRCh38.p7	3:20081150	GCCAAATTCCCATGA[A/G]CAAAAAATGTATTTG	8850
rs151203696	snp	C/T	0.00517822	0.0506191	intron-variant	KAT2B	GRCh38.p7	3:20052338	AGAAGCTCCATGAAG[C/T]GGAGATTTGGGTTCA	8850
rs151226942	snp	G/T	0.00438332	0.0466095	intron-variant	KAT2B	GRCh38.p7	3:20112049	TCTCTGACTCACATA[G/T]AATGGGGCAGTGCTT	8850
rs151252906	in-del	-/AT	0.259674	0.249813	intron-variant	KAT2B	GRCh38.p7	3:20065748	ACTCAAGGGATTCTC[-/AT]ATATATATCAATAGG	8850
rs151291624	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20064001	ATTGAATGGTCTTGG[C/T]ACACTTGTCAAAATC	8850
rs151336172	snp	A/C	0.000840772	0.0204861	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20101380	ATGTTCCTAAACCGC[A/C]TCAACTATTGGCATC	8850
rs180670618	snp	C/G	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20050183	CTAGCCTGGGCAATG[C/G]AGTGAGACCCTGTCT	8850
rs180815234	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20102854	TCCTGATTTAAAGTG[A/G]GCAGTAGTATCTTTT	8850
rs180820004	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20114403	ACACTGCCTATCATG[C/T]AGTAAGAGCTATATA	8850
rs180825357	snp	G/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20082618	GAATGTTTTAAATTT[G/T]AAAAACAAACTCTTT	8850
rs180827700	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20074450	GTTAATACATAGTAG[G/T]ATTTACCTTGCAGGA	8850
rs180830658	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20144731	GCTACTGAGGACTTG[A/C]TATGTGGTTAGTCAA	8850
rs180831120	snp	G/T	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20063573	TTTTTTTGAGATGGT[G/T]GCTCTGTTGCCCAGG	8850
rs180843614	snp	A/C	0.167158	0.235875	utr-variant-5-prime, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20040309	CCAGAGCGAGCCGGG[A/C]GAGCGGCGCGCTAGG	8850
rs180853978	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20092575	TTATATATATATTTT[A/G]TATATTTACAGCAAA	8850
rs180865280	snp	G/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20136795	GAAACGCAAGAAAGG[G/T]TGTTAATATATTTCA	8850
rs180866325	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20129502	ACCTCAGCCTCATGC[A/G]TAGCTGGGAACTATA	8850
rs180867030	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20096929	ATTTGGGGATATTAA[C/T]TTTAAAAAGAATAAT	8850
rs180868616	snp	A/G/T	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20059242	ACATGGTGAAACCCC[A/G/T]TCTCTACTAAAAATA	8850
rs180870387	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20123225	CTCCCCATGAACCAT[A/T]TGGAACCATTTCAGA	8850
rs180871046	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20079547	TCAAGAGTTAGCTTT[A/T]ACAATCACACTAGAG	8850
rs180874973	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20108087	AGTCCTGGGATTACA[A/G]GTGTGAGCCACTGCA	8850
rs180884221	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20062173	AATATATAATATATA[C/T]AATATATAATATATA	8850
rs180889507	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20045308	CAGGTGTGAGCCACT[A/G]CACCTGGCCTATTTA	8850
rs180889508	snp	C/T	0.00557542	0.0525036	intron-variant	KAT2B	GRCh38.p7	3:20086647	TGGGGTGCACACCCA[C/T]GCATATTCCTCATCA	8850
rs180900871	snp	A/G	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20150069	TGCTTGGTCCCACCC[A/G]TGAAGGTTGTGAACT	8850
rs180931884	snp	A/G	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20054855	GACTCATCCCACCTC[A/G]AAAGGAACACATCTG	8850
rs180969845	snp	C/T	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20068215	TGGCCAGGTTGGTCT[C/T]GAACTCCTGACCTCA	8850
rs181089554	snp	A/C	0.0185938	0.0946107	intron-variant	KAT2B	GRCh38.p7	3:20130058	GATCTGCTCACTGCA[A/C]CCTCCGCCTCCTGGG	8850
rs181101154	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20102965	AGCTTTCCTCTCTGA[A/C]ATTGACCTAGTTTCA	8850
rs181274730	snp	C/G	0.00835141	0.0640778	intron-variant	KAT2B	GRCh38.p7	3:20082885	TAACATCTTAAAAAC[C/G]AAGCAAAGGAACTCA	8850
rs181368689	snp	C/T	0.00358779	0.0422022	intron-variant	KAT2B	GRCh38.p7	3:20063952	GATACCTAGTTTTTC[C/T]AGCACCATTTATTGA	8850
rs181384533	snp	C/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20058822	AAGTTAATTCAGGGA[C/G]AAGAGAAAGGTGTTG	8850
rs181389650	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039351	TTTGAATTATGCTTA[C/T]ATCTTTTTCCTGGTT	8850
rs181397948	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20091535	TTTCTACTAACTTTG[G/T]ACTTTAGTTCGTTCT	8850
rs181486183	snp	C/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20150242	TTTTTTCTTGGTATT[C/G]TTCAGATGCTGAGTA	8850
rs181521291	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20050491	TACCAGAGATTAGTT[A/T]TGTCTGTTCTTAAAC	8850
rs181524275	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20073478	TCAGAGAGTATTTCA[A/G]TATTTACAGAGCATA	8850
rs181610365	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20144061	TTCTCCATACTGATT[A/T]CTAGAGGTACAGAGA	8850
rs181618899	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20114153	CTGTATTTCTAATAA[G/T]GTTTCCAGATGATTT	8850
rs181632906	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20092317	CACTGCAGCCTCCAC[C/T]TCACAGGTTCAAGTG	8850
rs181636292	snp	C/G	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20073965	CTAAGCACGTAAACA[C/G]ACATGAATGCCTGAA	8850
rs181647626	snp	C/T	0.00835141	0.0640778	intron-variant	KAT2B	GRCh38.p7	3:20059177	CAGCACTTTGGGAGG[C/T]TGAGGTGGGCAGATC	8850
rs181652106	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039594	TGACCCAGAAATTGC[C/T]ATGGGAAGAAAGTGT	8850
rs181698989	snp	C/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20108372	TAGAATCATCCCCAT[C/G]ATCAGTGAAAGCTTT	8850
rs181723330	snp	C/G	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20131284	CCTCCCAAAGTGCTG[C/G]GATTACAGTTGTGAG	8850
rs181740671	snp	A/G	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20083441	GATTGTCAGTATAGT[A/G]AATAGTTTAGCTTTG	8850
rs181790930	snp	C/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20138296	GTATTTTTTCTGTGT[C/G]TATATAAACATAAAA	8850
rs181818992	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20087230	AACACAAAGAAATGA[C/T]AAATATTTGAGATGA	8850
rs181822618	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20139589	TGAAATAGATACTTA[A/G]GGCAAATTATGTTTA	8850
rs181833536	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20109543	GGCTGGTCTTGAACT[C/T]CTGGGCTCAAGCGAT	8850
rs181834276	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20087447	GAGATGTATATATTA[C/T]AAAATGATTAAATCA	8850
rs181865349	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20056005	GTATTCTGCTGTATG[A/G]ACGTACTAGTTTGTT	8850
rs181936996	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20104118	TAATTATTTGAATAT[C/T]GCTTTAGAAATTAAG	8850
rs181994241	snp	C/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20149856	CTCTTTGTGTCCATT[C/T]CCAACCATAAATTAA	8850
rs181998658	snp	C/T	0.00438332	0.0466095	intron-variant	KAT2B	GRCh38.p7	3:20068565	CATAGCACCATCACA[C/T]TCTCCAGTATATTCT	8850
rs182003062	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20056789	TTTAGAATGCCACAG[A/G]GGAGTTCTAGGTTTT	8850
rs182228187	snp	A/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20096354	CTCCTCAAGCTTCTG[A/T]TTAGAGCCAGGACTA	8850
rs182234333	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20132260	ATGCCTGTAATCCCA[A/G]CTACTCAGAGGCTGA	8850
rs182234714	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20104550	TCAAAAATGGGTAAT[A/G]TTACTGGCTGCAGGC	8850
rs182239640	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20061632	TCTCTACATCCTCTC[C/T]AACACTGTTTTCTGT	8850
rs182248708	snp	A/G	0.00438332	0.0466095	intron-variant	KAT2B	GRCh38.p7	3:20084392	TATTTCATTCTCAGA[A/G]TAAGAGCTATCCTCT	8850
rs182250919	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20064325	ATGTTCATCACCTCA[A/G]TCACTTGTCATTTCT	8850
rs182262607	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20052821	AAAAAAACAAAAAGA[C/T]GAAAATTAGCCAGGT	8850
rs182280716	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20121784	TGTGTGTGTGTGTGT[A/G]TAGCCAAGCCCAGCA	8850
rs182299894	snp	C/T	0.00557542	0.0525036	intron-variant	KAT2B	GRCh38.p7	3:20062530	GCAGTGGCATGATCT[C/T]GGCTCATTGTAACGT	8850
rs182309969	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20046961	GACAACTCCCCCCAA[C/T]GAATGATTATCTGGT	8850
rs182434645	snp	C/G/T	0.00676609	0.0577691	intron-variant	KAT2B	GRCh38.p7	3:20075893	GCCTGGGCGACAGAG[C/G/T]GAGACTCCCATCTCA	8850
rs182442383	snp	C/T	0.00795532	0.062565	intron-variant	KAT2B	GRCh38.p7	3:20059483	AGCACTTTGGGAGGC[C/T]GAGGCAGGTGGATCA	8850
rs182475823	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20117849	CTAGCAAAGCAGCAT[C/T]CTACTTTGTACAATG	8850
rs182476211	snp	A/G	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20125687	ACATATAATACTCCA[A/G]TTTCTCAAAATGCTT	8850
rs182477373	snp	C/T	0.000364269	0.0134908	intron-variant	KAT2B	GRCh38.p7	3:20140390	GGTTGACTCCCTTAC[C/T]TTCTGTACAGGCCAG	8850
rs182486173	snp	A/G	0.000417875	0.0144486	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20099877	CTCTTGAGAAAGTCT[A/G]TTTTACAAAGAGGAA	8850
rs182493526	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20081188	TTCAAATCCTATTGT[A/G]TTATTTGCTTCTGGT	8850
rs182498117	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20077188	TAGGAAGTAATAATT[C/T]TAGCCTGTCTGGGTA	8850
rs182499329	snp	A/G	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20078601	CTGGGCTGGTCTCAA[A/G]CTCCTGAGGTCAAGC	8850
rs182531200	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20133709	AAAAATTATTTCCAG[A/C]TTGTCTTCTCAGTGG	8850
rs182539870	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20105790	TGGGTGACAGAGCAC[A/G]ACCCTGTCTGAAAAA	8850
rs182583777	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20088452	AATAGCTATCCTGAG[C/T]GTGAAGTGATATCTC	8850
rs182602911	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20057287	TGACTGGGCAGAAAT[C/G]CTGGATGTAAGCAGT	8850
rs182624854	snp	A/G	0.00835141	0.0640778	intron-variant	KAT2B	GRCh38.p7	3:20041235	CTGGGTGCAAGGAGT[A/G]GGGGTGGAGAAGACT	8850
rs182740822	snp	A/G	0.0021958	0.0330617	intron-variant	KAT2B	GRCh38.p7	3:20148011	AAAGGTAAGTATGAC[A/G]GGCAAGAGGATGTTA	8850
rs182754801	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20094859	TCTGCATCTCTGAAC[C/T]ACCAACTTACAAGTC	8850
rs182767894	snp	C/G	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20060321	CTTAAAAAACTGTGG[C/G]CTGGGCATGGTGGCT	8850
rs182823094	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20145190	TGACATTTTAGATAT[A/G]ATGGGTTAAATGAAA	8850
rs182833061	snp	C/T	0.0111196	0.0737302	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070957	GAGGATGCAGTGAGA[C/T]AAGATCTTGCCACTG	8850
rs182839346	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20124106	AAAATTGATCTTTCC[A/G]TTTCCTCCTAGATGT	8850
rs182840536	snp	A/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20065763	CATATATATCAATAG[A/G]GTATAACTTTAAAGA	8850
rs182841084	snp	C/T	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20098725	ACCAATCTTTAGATA[C/T]TCTTAGAAACATATA	8850
rs182844471	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20057886	AATTATAATATTTAG[C/G]AAAGGGAGGGCAGTT	8850
rs182846999	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20080089	GGAGTTCTTATTTCC[A/G]TTCCTGCATACCTGG	8850
rs182855622	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20111052	TTTAAATAAATCTTA[C/T]ATTTTACTCAAAGGA	8850
rs182857046	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20062331	TAAAATATTTATTAT[A/G]TATAAAATATAATAT	8850
rs182871454	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070285	TACCTTGCCAATCGT[C/T]TATTCTCTTTTCTTT	8850
rs182891979	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20075982	CTTTCTTGTAGATTG[A/G]TGGGTGGGGTTGAAG	8850
rs182901864	snp	A/G	0.00358779	0.0422022	intron-variant	KAT2B	GRCh38.p7	3:20059963	CTTTTCTGGATGGTC[A/G]TGTAAATGGAAGTAT	8850
rs183012523	snp	A/C	0.00716266	0.059414	intron-variant	KAT2B	GRCh38.p7	3:20151618	GAGGATTGAAGAAAC[A/C]CTACTTTAGTTTTAT	8850
rs183038387	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20146158	TGGTATAATATAATC[C/T]GTTCATTTCTTACTT	8850
rs183055950	snp	A/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20116540	GGACATTGGGACTTT[A/T]AAAAAGCTCCCCAGG	8850
rs183059205	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20094382	ATCACTTCCCAGCAG[A/G]TCCCTCCCTTGACAT	8850
rs183140087	snp	C/T	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20084676	CCTCCTCAGGTTTCA[C/T]TTAAGCATTTTAATT	8850
rs183144836	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20115784	TGCATTCATAGTCCT[A/G]CCTCCAGCTCTGGGA	8850
rs183346823	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20111517	CTATAGTTAATAGTA[C/T]GAGATAAACATAATT	8850
rs183407953	snp	C/G	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20046019	GGCACAGGTCACTTA[C/G]TTTTTCTCTGAGCCT	8850
rs183478909	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20051419	AATATTCATGTGAAA[C/T]CCTGTTGCCACTTGT	8850
rs183542974	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20086336	GGGCATGGTGGCTTA[C/T]ACCTGTAATTCTAGC	8850
rs183561954	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20067703	CTTCTGAGACAGGGT[C/T]TCACTCTGTCACCCA	8850
rs183565814	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20054426	GTGAAGGAGATGGAT[A/G]CATTTATTTTGGAAA	8850
rs183585924	snp	G/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20140957	CCATTTTGCATTCTG[G/T]CCTCAATTATTGTTC	8850
rs183703927	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20042054	ATCTAGCCCAGTGCT[C/T]CTCAAACTTTAATGT	8850
rs183705024	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20099254	ACGGATGGAAGGGAA[A/G]TGAAAAAAAGACTGT	8850
rs183708965	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20064077	GTTCCATTAGTATAT[A/T]AGAAGCTAGCAAACT	8850
rs183750137	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20129617	CTGACCTCAGGTGAT[A/C]TGCCCTCCCTGGTCT	8850
rs183751517	snp	A/G	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20102873	GTAGTATCTTTTGAT[A/G]GCCTGTCAAGACCAC	8850
rs183804247	snp	A/G	1.78112e-05	0.00298417	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20136914	TCCCCAGTCTAATGT[A/G]TTTGTTTGTATACTA	8850
rs183907464	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20125523	ACCCATTCTTTAACA[C/T]ATTGTCTGTGGATGC	8850
rs183933900	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20080411	TCCTCCAAGGCTTGA[C/T]TGCAGAACTCTGTAG	8850
rs183944524	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20046308	AAATAGGCCCAGGGC[A/G]TGGTGGCTTGTGCCT	8850
rs184009443	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20095715	ATGTGGCACTAACGT[A/G]GGCATGAGGGATAGA	8850
rs184012135	snp	C/G/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20078216	TAAATAAAAAGGCAG[C/G/T]CTGTTTTTACGAGCA	8850
rs184027231	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20060475	GCATGGTGGTGCATG[A/C]CTGTAATCCCAGCTA	8850
rs184036597	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20043444	TCTTGGAGTAGTTGC[A/G]GACCCAGAGCAGGAC	8850
rs184260012	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20091681	TTTGTAAGTTTTGGT[A/G]TATTGTATTTCCACT	8850
rs184261586	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20126980	AGGATTCCATAATGC[A/G]GAATTTTGCAAATTG	8850
rs184263350	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20153298	CATAAGTTCCAAAAG[A/T]TAATTTCCCTGCCCA	8850
rs184293349	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20042894	AGAAAGAGAAAATTT[A/G]TTTTAACGTCTTTTT	8850
rs184336507	snp	C/T	0.00358779	0.0422022	intron-variant	KAT2B	GRCh38.p7	3:20054192	TGCAGTGCAGTGGCG[C/T]GATCTTGGCTCACTG	8850
rs184439541	snp	C/T	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20073691	AAGTTAGAGAACTGT[C/T]CTTGATTATAATTTA	8850
rs184448213	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20059027	TACTCCTAATTACAT[A/C]AGCATAATTCAAACT	8850
rs184450164	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20100818	CAAACAAATGATAGT[A/T]AAGAGTTTAAATTTT	8850
rs184456324	snp	C/T			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039410	AACTACGTAACGTTA[C/T]AGAACCACCACCCAG	8850
rs184511239	snp	A/C/T	0.00795532	0.062565	intron-variant	KAT2B	GRCh38.p7	3:20141993	AGCAGCACATCGTTC[A/C/T]GCATTAGAGGCTGCT	8850
rs184519814	snp	A/G	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20091117	GAATTCAGCCTTGAA[A/G]CCATCAGGTCCTGGG	8850
rs184539116	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20058757	GAAGAAAAAGGGCTT[A/G]TGTCCCAGGGAAGGA	8850
rs184553288	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20112129	GTTTAGGTACATTTT[A/C]CAGCCACTCAGAAAT	8850
rs184563219	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20108105	GTGAGCCACTGCACC[C/T]GGCCAAATCCAGTGT	8850
rs184565773	snp	A/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20148601	GGTAGGAAGTGTATG[A/G]CGGGTGGTGGGATTC	8850
rs184569089	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20090844	GGGTGGGTTCAAGCA[A/G]TCCTCCAACCTCAGC	8850
rs184573877	snp	A/C	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20072634	CTTCTCGTGAGAGAC[A/C]AATGCTGCACTGTGT	8850
rs184581472	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20068239	GACCTCAGGTGATCC[A/G]CCTGCCTCGGCCTCC	8850
rs184582122	snp	A/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20058379	AGAATTGCTTGAACC[A/T]GGGAGGCGGACATTG	8850
rs184649551	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20113128	AGGGAGATTCTGAAG[C/T]ACTTAAACTGCAGTT	8850
rs184660403	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20073413	TACAAGAAATGGTGT[C/T]GCCTCCAAGGTTAGC	8850
rs184677756	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20148991	CCATGCCCTTGATGG[C/G]TACTGTTAATGTCAC	8850
rs184679737	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039018	AAGGGGAATGTTTCC[A/C]ACGAAAAGCACACCC	8850
rs184684262	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20119478	TTGTGGCTTATGTTT[C/T]AAAGATGACTTATTT	8850
rs184686386	snp	G/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20096209	ATTTATTTTGGTAAC[G/T]TAGCCACTGTTACCT	8850
rs184700295	snp	C/T	0.00676609	0.0577691	intron-variant	KAT2B	GRCh38.p7	3:20078461	TACTGCAACCTCCCC[C/T]TCTTGGGCTCAAGCG	8850
rs184703657	snp	A/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20086903	TCTCCTGCCTCAGCC[A/T]CCCAAGTAGCTAGGA	8850
rs184707874	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20118252	ATATTTACATTTTTA[C/T]AAAAATATGTAAATA	8850
rs184721436	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20054878	CACATCTGTGAGCAC[C/T]GGTTAGGGGCCTGTG	8850
rs184771785	snp	C/T	0.0126979	0.078662	intron-variant	KAT2B	GRCh38.p7	3:20134607	AGAGATGGGGTTTCA[C/T]CATGTTGTTCAGGAT	8850
rs184787029	snp	A/G	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20107409	ACGCCAGTAATCCTA[A/G]CACTTTGGGAGGCCA	8850
rs184861703	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20113791	TACATTCTTATCTTC[C/T]TATTCTTCATATGTG	8850
rs184951165	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20143686	GTACATATACACCAT[G/T]GAATATTATGCAGCC	8850
rs185084918	snp	A/T	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20081780	AATAATTAAAAATTT[A/T]CATAAAAGTCATGAG	8850
rs185104187	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20048375	GACTGTTTTGTTTTA[C/G]GAAGTGTGTGCTTGG	8850
rs185212919	snp	C/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20062756	CGTGAGTCACCGTGC[C/G]TGGCCCATTTTCATA	8850
rs185227086	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20082695	GAAAAACCTTTGCAA[A/G]CAAAACCTTAAAGAA	8850
rs185232153	snp	G/T	0.00636936	0.0560724	intron-variant	KAT2B	GRCh38.p7	3:20063655	TCAAGCAATTCTCCT[G/T]CCTCAGCCTCCCAAG	8850
rs185242344	snp	A/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20050276	CAGTATCTCAACATG[A/G]TAAAAAGGAGTCATT	8850
rs185280549	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20079645	ATTTAGGCAGATCAT[A/T]TGACTCAACACATTT	8850
rs185284563	snp	A/T	0.0119091	0.0762411	intron-variant	KAT2B	GRCh38.p7	3:20062282	ATATATAATATATAA[A/T]ATATAATATATAATA	8850
rs185295419	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20045519	CCATGCCTGCTTGGG[A/T]TTGGGTTTTTAATGT	8850
rs185340443	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20133824	ACGTATTTGCACGCC[A/G]TCAAGTGCAATATTT	8850
rs185342577	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20061269	ACTTAGCATAACATT[C/T]TCAAGTTTCATTCAG	8850
rs185354991	snp	A/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20085447	TAGTCAAACAGCAAA[A/T]AATATATTTAAACAT	8850
rs185372937	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, downstream-variant-500B	KAT2B	GRCh38.p7	3:20154404	TTTAAAAAGCTTCCA[A/G]TCTTGTGGTGTGTTT	8850
rs185394712	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20101959	ACTAGATAGCTACAC[C/T]ATAACTCTGAAATTA	8850
rs185407998	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20063367	TTTTGGTATTATATC[C/T]AAGACACCATTGCCT	8850
rs185461242	snp	G/T	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20123383	TATTTTCTAATACAG[G/T]GTTGGTGAATTACAG	8850
rs185467879	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20106682	TGTCTTCTACCCTGG[A/G]AAGATTGAATAACCT	8850
rs185472429	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20043550	GCAGGGCAGAGTGGG[A/G]TGGGGTGAAGCTTCT	8850
rs185477712	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20066877	ATGTGATATTTTAAC[A/G]TTTTTTAATACGAAG	8850
rs185501097	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20129327	AGGCATTCAATGTCA[C/T]GAAGAATTATGGAGA	8850
rs185521363	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20082071	ATGGAGACCCACTCT[C/G]TTGCTCAGGCTGGAG	8850
rs185521681	snp	A/G	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20116106	TTCTAACCTGAGATC[A/G]TAATTTCATGTATCT	8850
rs185525625	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20130209	GGAGCTTTTTGTCTT[C/T]GACTCCTAGCACTAA	8850
rs185525940	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20093749	TTTAATCTTCAAGCA[C/T]TTTTAAGCCAGCACA	8850
rs185541877	snp	C/T	0.0115144	0.0749975	intron-variant	KAT2B	GRCh38.p7	3:20049022	CCCCGCCACCACGCC[C/T]GGCTAATTTTTGTAT	8850
rs185861991	snp	A/C	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20044514	TTGTGGTCCACAAGG[A/C]CCTGCATGGCCTGGC	8850
rs185969568	snp	G/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20124644	AAACTACATCAGGAT[G/T]CAGTCACATGTTTGA	8850
rs185973596	snp	A/G	0.00716266	0.059414	intron-variant	KAT2B	GRCh38.p7	3:20151355	ACCTTATTAAATGAT[A/G]ATCCCAATGTATTTG	8850
rs185985620	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20098743	TTAGAAACATATACA[A/T]TGACTTATCTTTATT	8850
rs186073621	snp	C/T	0.00478085	0.0486577	intron-variant	KAT2B	GRCh38.p7	3:20144886	CTGCAACCTCCACCT[C/T]CCAGGTTCAAGCAAT	8850
rs186087891	snp	A/G	0.00358779	0.0422022	intron-variant	KAT2B	GRCh38.p7	3:20092768	GTGCACTGGTGTGAT[A/G]TCGGCTCACTGCAAT	8850
rs186104845	snp	A/G	0.00358779	0.0422022	intron-variant	KAT2B	GRCh38.p7	3:20059346	TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGC	8850
rs186205328	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20114495	AAGTTCTTAGAGCAG[A/T]GCAGGCACAAAGCAA	8850
rs186227781	snp	A/G	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20075396	TCCCACTCTCTGAAC[A/G]CTAGCTGGAGGTCCC	8850
rs186242463	snp	C/G	0.0197687	0.0974348	intron-variant	KAT2B	GRCh38.p7	3:20040847	CGGGACCCCCCTCCC[C/G]CTCCCGCTTCCACCT	8850
rs186251871	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20056526	TCTGGGACATTCTGA[A/C]TGCCTCATAGATGTC	8850
rs186286826	snp	A/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20114258	TCCTGCCATTTACTA[A/G]TTGTGGGAATTTGAT	8850
rs186287670	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20064160	TCCAATTTTTCACAT[A/G]CCTGATAATTTGTTA	8850
rs186292509	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20051673	TAAATGCCACCCTCT[C/G]CCCAGGAATGACAGT	8850
rs186292920	snp	C/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20092418	CATTTTCAGTAGAGA[C/T]GAGGTTTCACCATGT	8850
rs186294058	snp	A/T	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20074087	CATAATCAAGAATGA[A/T]GAATGAAAAAAAAAA	8850
rs186328694	snp	C/T	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20150088	AGGTTGTGAACTTCT[C/T]CAGTTGGATACCACC	8850
rs186450404	snp	A/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20082891	CTTAAAAACCAAGCA[A/G]AGGAACTCAAATTGG	8850
rs186467009	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20050549	AATTATTTGTGTCTG[A/G]GTTCTTTCACTCAAC	8850
rs186469242	snp	C/T	0.00874735	0.0655527	intron-variant	KAT2B	GRCh38.p7	3:20139977	TTCTGTTTTAAACTT[C/T]TTAATATTTCTTGCA	8850
rs186476663	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20109802	ATTAACACTTAAGAT[A/G]CCCATTTCAGTATTG	8850
rs186490442	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20087644	TTTGTACTCTGTGAC[C/T]AGCATCTCTACCCGT	8850
rs186494854	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20069377	TTCCCCTGGTACCCT[A/G]TCTGGGCTGATAAAG	8850
rs186502739	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20056906	GTTGTTGGGAGGGGA[A/G]CATAACATGATTTGG	8850
rs186511550	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20140533	CACAGAGTCTCTCTG[C/T]CACCTAGACTGGAGT	8850
rs186583210	snp	A/C	0.00874735	0.0655527	intron-variant	KAT2B	GRCh38.p7	3:20145209	GGTTAAATGAAATAC[A/C]TTATTAAAATCAATT	8850
rs186620620	snp	C/T	0.00398564	0.0444627	intron-variant	KAT2B	GRCh38.p7	3:20103492	ATAGCTCACTGTAGC[C/T]TCAACCTCCTAGACT	8850
rs186652414	snp	C/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20064023	GTCAAAATCATTTGA[C/T]CATTATCTGTGAGGG	8850
rs186900581	snp	C/T	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20105099	CCATGTTGGCCAGGC[C/T]AGTCTCGAACTCCTG	8850
rs186904893	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20084425	TGCTATGAAAGTTAC[C/T]CACCCTTTGTACAGG	8850
rs186909080	snp	C/G	0.00438332	0.0466095	intron-variant	KAT2B	GRCh38.p7	3:20043133	TGTTCTCAAACTCCT[C/G]AGCCCAAGCAATTTG	8850
rs186909726	snp	G/T	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20138745	TAAAAATGTTTAGTT[G/T]TACATTGATTTGTGA	8850
rs186916059	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20064935	TGTTCCTCTGGATGC[C/T]ACTCAAATATCTTCA	8850
rs186917948	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20062368	TATTTTATATATAAT[A/T]TATAATATATTATAT	8850
rs186925482	snp	A/G	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20087256	GATGATGGATATGCT[A/G]ATTACACTGATCTGA	8850
rs187013033	snp	G/T	0.00398564	0.0444627	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039999	GCGGTAGGTGTCGAA[G/T]CACTGGGGTGGGGGG	8850
rs187077089	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20059500	AGGCAGGTGGATCAC[A/G]AGGTCAGGAGATCGA	8850
rs187084255	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20041593	TGGAGGCTGTGTTCC[C/T]GAGGTGGGAGGATTG	8850
rs187100683	snp	A/G	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20080138	ATACAATGTGATCCC[A/G]TTCTCCTGCTTAACC	8850
rs187107183	snp	A/G	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20108802	GTCAGATCAGTGGTG[A/G]CATTAGATTCTCATA	8850
rs187115541	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20152267	GATTCCTTTCCCAGT[C/T]CCAGTTTTGTCAGCT	8850
rs187121035	snp	A/G	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20100194	GTGTGTTTGGGGAAG[A/G]AAAACATTAAGTAGA	8850
rs187121981	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20046192	TCAGAGTCAGTGGCC[A/G]CAAAGCATTTATGGA	8850
rs187122557	snp	A/G	0.00557542	0.0525036	intron-variant	KAT2B	GRCh38.p7	3:20126639	ACCAGCCTGACCAAC[A/G]TGGAGAAACCCCGTC	8850
rs187131732	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20081510	GATCTAAAGAAGGCA[A/G]AGCCTCCCCTCGTCC	8850
rs187137143	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20062651	GTTTTTAGTAGAGAC[A/G]GGGTTTCGCCTTGTT	8850
rs187142334	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20047306	TGAACTCCTGGGCTC[A/G]AGCAATTGGCCTGCC	8850
rs187176400	snp	A/T	0.00398564	0.0444627	intron-variant	KAT2B	GRCh38.p7	3:20104461	TCGGAGTAAAACCTC[A/T]CTGCCATGACCACAT	8850
rs187215406	snp	A/T	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20059201	GCAGATCACTTGAGG[A/T]CGGGAGTTCGAGACC	8850
rs187276504	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20122125	AATTCATAGGTCAAA[C/G]AGACAAAAATATCAG	8850
rs187307481	snp	G/T	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20078978	AACTTCCGCCTCCCA[G/T]GTTCAAGCAATTCTC	8850
rs187373789	snp	A/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20131621	TGCCCAGGCTGGAGT[A/G]CAGTGGCATGATCAC	8850
rs187380448	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20083639	TAGGAAGACTACCCT[A/G]GCAGCAGAGAGAACA	8850
rs187403856	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20128150	GGATACTGTACAAGT[G/T]CAATATGTAACTCAA	8850
rs187406655	snp	A/G			utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20153409	ATCTGGTGAATCCTC[A/G]TTCTAATAAAGGTTC	8850
rs187464788	snp	A/G	0.00557542	0.0525036	intron-variant	KAT2B	GRCh38.p7	3:20090235	GACTTCCAATACTAC[A/G]TTGAAAAGAAGTGGC	8850
rs187473362	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20149881	AATTAACTGATTTTT[A/G]CATCCTCTTCCTCTG	8850
rs187476278	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20071736	TGGGAAATGTACGTG[C/T]AAGTAGAAACCCAGG	8850
rs187480336	snp	G/T	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20058118	ACTCTTTAATATTTG[G/T]TTTTTTGATTCCTTG	8850
rs187501299	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20096444	TAGATCTATAAAGGA[A/G]GCTGCCAGAAGGAAT	8850
rs187505763	snp	C/T	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20148157	GTTCCAATTTCAGGT[C/T]TTTGTAAGAATGAGC	8850
rs187511076	snp	C/T	0.00478085	0.0486577	intron-variant	KAT2B	GRCh38.p7	3:20095204	CCTTCCACTTAAAAA[C/T]GGGGAATGTTTGGTT	8850
rs187574594	snp	A/T	0	0	intron-variant	KAT2B	GRCh38.p7	3:20061726	TTTCATACGTATATA[A/T]GAAAAAATAATATAT	8850
rs187689690	snp	C/T	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20060391	CGGATCACCTGAGGT[C/T]GGGAGTCTGAGACCA	8850
rs187726337	snp	C/G	0.0142736	0.0832652	intron-variant	KAT2B	GRCh38.p7	3:20085685	CCGGCTATTTTTTGT[C/G]TTTTTAGTAGAGACA	8850
rs187728124	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20146271	GACTTGAACTGTATC[C/T]ATAGACTTCTTTCCC	8850
rs187731576	snp	C/T	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20116799	ATCTCCTTTACATAG[C/T]TGAGGAAATAGAAGC	8850
rs187733510	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20067164	AATATACTTTGTACT[G/T]GGATCCCAAGACTCA	8850
rs187734180	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20094396	GGTCCCTCCCTTGAC[A/T]TGTGGGGATTGCAAT	8850
rs187739441	snp	C/T	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20054285	AGGGGTCTGCCACCA[C/T]ACGCAGCTAATTTTT	8850
rs187757144	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20117936	AGAGTTACAAGAAGA[A/G]GACAAAGAAATCCTG	8850
rs187759742	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20141543	ATACTTCTGTTATTC[A/G]TTTAGTGCACTTTTC	8850
rs187769328	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20112467	TTGCAGTGCTGCACC[A/T]TTGGCCTTGGAAATG	8850
rs187785398	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20090854	AAGCAATCCTCCAAC[C/G]TCAGCCTCCTGAGTA	8850
rs187787349	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20073196	AAAATTTCAGTCCAC[A/G]AAGAATCTTAGACTA	8850
rs187960061	snp	C/G	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20046385	TCACGAGTTCGAGAC[C/G]AGCCTGGGCAACATG	8850
rs187960754	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20111212	TCATTTAATGCTCAC[A/G]AGAACCCAATGAAGT	8850
rs187972140	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20077561	TGAAGACATCATAAG[C/T]AAAAACAATGCAGAA	8850
rs187976546	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070599	GTGACCCACCGTGCC[C/T]GGCCTCTCTTTTCTT	8850
rs187993966	snp	C/G	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20133794	CATTGCTGGCACTGG[C/G]TACATAAACTGTAAA	8850
rs188007194	snp	C/T	0.00716266	0.059414	intron-variant	KAT2B	GRCh38.p7	3:20135546	GTAGTCCCAGTTATT[C/T]GGGAGGCTGAGGCAG	8850
rs188014308	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20085027	GTATACTGATTGCTT[C/T]CATAGCTTATCACAA	8850
rs188022955	snp	C/T	0.161924	0.233971	intron-variant	KAT2B	GRCh38.p7	3:20061927	ATATGTATTATATAT[C/T]ATATATAAAACATAA	8850
rs188027156	snp	A/G	0.00358779	0.0422022	intron-variant	KAT2B	GRCh38.p7	3:20107487	ACATGGTGAAACCCT[A/G]TCTCTATTAAAAATA	8850
rs188033277	snp	G/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20086636	AAATGCTGTATTGGG[G/T]TGCACACCCATGCAT	8850
rs188033316	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20045182	ACCATACTTGGCTAA[C/T]TTTTGTATTTTTTTT	8850
rs188034989	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20054085	TTACAGGCATGAGCC[A/T]TTGTGTCCGGCTTTA	8850
rs188040320	snp	A/C	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20067826	ATTACAGGTGCCCAC[A/C]ACCACACCTGGCTAA	8850
rs188066135	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20057381	CATCTCAGATAATGA[C/T]TGATACCATGAGAAC	8850
rs188245531	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20088691	TCTTCCATTCCATAG[A/G]TTGTCTCTTTACTCT	8850
rs188270150	snp	A/C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20141088	CACACATAAATCAAA[A/C/T]CGTTTCAGGGTGTGT	8850
rs188290708	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20106365	ACATGTGCTCATGCA[C/T]GTCCGTTTCCTTCTT	8850
rs188307148	snp	A/G	0.00358779	0.0422022	intron-variant	KAT2B	GRCh38.p7	3:20066457	TAGCTGGAGTGCAGT[A/G]GTGCCATCTCAGCTT	8850
rs188466667	snp	A/G	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20130004	TATTATTTTGAGACA[A/G]AGTCTTGCTCTTTTG	8850
rs188469645	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20102907	TGCCCAGGTTATTTT[C/T]TGTAACAGCAGATAA	8850
rs188473712	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20082802	CCACCAAATACGTAA[A/G]CATTTGCAATGAGTA	8850
rs188486241	snp	C/T	0.00716266	0.059414	intron-variant	KAT2B	GRCh38.p7	3:20063840	GCCACCACGCCCGGC[C/T]GAGATTCACAATTTT	8850
rs188494112	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20050472	TCCTTATTCTGACTT[C/T]TATTACCAGAGATTA	8850
rs188558836	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20111827	TTGTTTGATCCCAGA[A/G]CTTGAGGTTGCTAAA	8850
rs188678877	snp	C/T	0.00755907	0.0610114	intron-variant	KAT2B	GRCh38.p7	3:20119314	TAACTACCATAACTC[C/T]GTCCTTATTTCTTTG	8850
rs188693171	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20095956	GAAGTTGAGCAGAAA[C/T]CTGAGTGGGAGATAG	8850
rs188695320	snp	A/G	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20078280	ATAATTGGAATTTCT[A/G]TTGTTATTTTGGAGT	8850
rs188705008	snp	A/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20060699	GGAGGCTGAGGTGGG[A/G]AGATCCCTTGAGTCC	8850
rs188716828	snp	G/T	0.00795532	0.062565	intron-variant	KAT2B	GRCh38.p7	3:20043509	GGCTTCCTGGAGGAA[G/T]TGTCAGTGGCTGCTA	8850
rs188758906	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20076071	GTTATCTGTGCACTA[C/T]CTTAAGTCACCTCAT	8850
rs188774540	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20042135	TGGTCTGAGGTGGAA[A/G]CTGAGAGTTTGCATT	8850
rs188800951	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20125602	CTCACAACGTCTAAA[A/G]TATTTTCTATCTGGC	8850
rs188821811	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20080616	TTCAATAATGGTAAA[A/C]TGAGGGCTGGTTGCA	8850
rs188862740	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20148603	TAGGAAGTGTATGAC[A/G]GGTGGTGGGATTCCA	8850
rs188934957	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20114130	ACCTGCCCTATTCTG[A/G]TAAGCATCTGTATTT	8850
rs188936909	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20092127	CAGTGCTTTGTCATT[A/G]ATTTTCTGTGTAAAT	8850
rs188946329	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20073913	ACATTTAAAACAGGA[C/T]CTTCTTTCTTTCTTA	8850
rs188956833	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20059085	CAATCCCAGCTGCTT[A/G]CAGTGGACTCCAGGT	8850
rs188964922	snp	A/G	0.00318978	0.0398085	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039424	ATAGAACCACCACCC[A/G]GAAACGAATCCTGTT	8850
rs189000352	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20134118	TTGAAGTATTCTACT[C/T]AATAATCAGTCTTTT	8850
rs189006059	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20149893	TTTGCATCCTCTTCC[A/T]CTGGACCATCTCAGC	8850
rs189027063	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20096716	CTTTTGCTTTGGCTG[C/T]TAGGAATCTTAGTGC	8850
rs189045485	snp	C/G/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20060078	TTCTTTATCTTTCAT[C/G/T]GCAAGTAATAATCCG	8850
rs189110619	snp	A/G	0.0486741	0.148216	intron-variant	KAT2B	GRCh38.p7	3:20062430	ATATTATTATATATA[A/G]TATATAATATATAGA	8850
rs189306316	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20122542	TCCTTTGTCACCCCT[C/T]CCCCTGGTGGTAAAG	8850
rs189316120	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20079111	TTGCCAAGTTAGCCA[C/T]GCTGGTCTCAAACTC	8850
rs189344196	snp	C/T	0.00716266	0.059414	intron-variant	KAT2B	GRCh38.p7	3:20063432	TTTTAAGAGATTCTT[C/T]CTTTCTTTCTTTTTT	8850
rs189350721	snp	G/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20054519	GGTTTAGGGTAATCT[G/T]GTCAGTAACCTCAGG	8850
rs189387027	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20120449	GTCAGGCTGGTCTCA[A/T]ACTCCTGACCTCAGG	8850
rs189391020	snp	A/T	0.0119091	0.0762411	intron-variant	KAT2B	GRCh38.p7	3:20149283	ATCTATTCCAGGTGC[A/T]AAGAACTGTGAAAGT	8850
rs189525028	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20073442	GCATGGTGTTAGGTC[A/G]TCTGAAATTTTATTT	8850
rs189541521	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039348	TCTTTTGAATTATGC[C/T]TATATCTTTTTCCTG	8850
rs189585848	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20055622	GACCTGTGTGGCTAG[A/T]TGGAGGTGGGTGGGG	8850
rs189625717	snp	A/G	0.00517822	0.0506191	intron-variant	KAT2B	GRCh38.p7	3:20144559	CTCCCAAAGTGCTGG[A/G]ATTACAGGCGTGAGC	8850
rs189630099	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20114300	ACTTCTCTGTGCCCT[A/T]GTTTCTTCATCTGTG	8850
rs189632188	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20092467	ACTCCTGACCTCACA[G/T]GATCCACCCACCTTG	8850
rs189678221	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20110320	CATGGCTACCACTGT[G/T]ATATTTATGTTTTTG	8850
rs189690712	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20087697	TAACCATCATTTTAC[C/T]TTCTGCTTCTGTGAT	8850
rs189779571	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20142268	TTCTCCTCTCCTCCC[C/G]CTCTGCCTCCAGCCT	8850
rs189780762	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20138272	AATGCTTTGACATAA[A/G]TCTTTTTAGTATTTT	8850
rs189787069	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20087206	AGATGGATGATACCG[A/T]GTGTTTCCAACACAA	8850
rs189795733	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20091346	GTGGTATCAGTTATA[A/G]TGTCTCCTTTTTCAT	8850
rs189810048	snp	C/T	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20058761	AAAAAGGGCTTGTGT[C/T]CCAGGGAAGGATTAC	8850
rs189832952	snp	A/G	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20143709	ATGCAGCCATAAAAA[A/G]GAACAAAATCATGTC	8850
rs189853455	snp	A/C	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20068312	TGTCTGGTTTAATTT[A/C]AACACGTCTTTACCC	8850
rs189867167	snp	C/T	0.00517822	0.0506191	intron-variant	KAT2B	GRCh38.p7	3:20101844	GGATTAAATAAAATA[C/T]ATTGAAGTTAATTTT	8850
rs189914689	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20133050	TTTTTTAGAAATAAT[G/T]TTTAATTATGTAAGA	8850
rs189933237	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20105331	CATGAAGAAATAACC[G/T]AAAAAGAAAGTGTCA	8850
rs189935771	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20084515	TCCATCTCCCTATTC[C/G]TTTCTACTTTGGGTT	8850
rs189945140	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20065645	TTAAAAATTTTGTAC[A/G]CTTAGGTTGTTAGGT	8850
rs190035368	snp	G/T	0.00398564	0.0444627	intron-variant	KAT2B	GRCh38.p7	3:20108117	ACCCGGCCAAATCCA[G/T]TGTGTATTTTTCACA	8850
rs190039233	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20041032	CGCTTGAAAGGAGTA[A/G]CTTCGGCATCCGAGC	8850
rs190105619	snp	A/G	0.00438332	0.0466095	intron-variant	KAT2B	GRCh38.p7	3:20045857	TAACAGTGAGGATTT[A/G]AAATGGGCTGTATTA	8850
rs190254249	snp	C/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20150129	GCTGAGTCTCACAAG[C/G]GGGGAAACTGACCTA	8850
rs190269162	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20123418	CAAGCCAAATCTGCT[C/T]CACTGGCTGTTTTTT	8850
rs190272966	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20098626	CCAAATTGAAACCCC[C/G]AAATGGGCCAAGTTC	8850
rs190289873	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20079891	AGCTGTGGGTCGGGC[A/G]CAGCAGGAGTTAAGG	8850
rs190296173	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20062296	AAATATAATATATAA[A/T]ATATAAAATATAATA	8850
rs190306110	snp	A/G	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20145221	TACATTATTAAAATC[A/G]ATTTCACCTGTTTCT	8850
rs190317339	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20116457	CCATGGAATTTGAAA[G/T]GCACTGTATACTGTT	8850
rs190324808	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20078518	GCTGGGACCACAGAC[A/G]TGCAGCAACATGCCC	8850
rs190329999	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20094082	TATTTAGTCTGTCTG[A/C]GACTGTATTAGTTCA	8850
rs190339755	snp	C/T	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20075936	AAAATTTTTTTCATA[C/T]GGCTTTATCTCTACA	8850
rs190344884	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20048381	TTTGTTTTAGGAAGT[A/G]TGTGCTTGGAAATAG	8850
rs190353920	snp	G/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20041594	GGAGGCTGTGTTCCC[G/T]AGGTGGGAGGATTGC	8850
rs190390959	snp	A/G	0.00716266	0.059414	intron-variant	KAT2B	GRCh38.p7	3:20082322	TTACAGGCTTGAGCC[A/G]CTGCACCCGGCCACG	8850
rs190573770	snp	G/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20096353	TCTCCTCAAGCTTCT[G/T]ATTAGAGCCAGGACT	8850
rs190580495	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20151410	AATTTTATAACATAC[C/T]TATAATTTGGGATAT	8850
rs190585538	snp	C/T	0.0130921	0.0798413	intron-variant	KAT2B	GRCh38.p7	3:20129362	TTACATTACATTCTT[C/T]GTTCTGTACTGTCTT	8850
rs190633333	snp	A/G	0.0166325	0.0896639	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20069776	CCTCATGATCCACCC[A/G]CCTTGGCCTCCCAAA	8850
rs190643046	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20102556	CATTTCTCTATTGCT[A/G]GACATTCAAACTCTG	8850
rs190772077	snp	A/G	0.00358779	0.0422022	intron-variant	KAT2B	GRCh38.p7	3:20151558	TAGACAAATGTTAGC[A/G]TCTATTCTAATCTGC	8850
rs190811668	snp	A/G	0.00119737	0.0244387	downstream-variant-500B	KAT2B	GRCh38.p7	3:20154555	ATCCATAGGTCATCA[A/G]TAAGAGATTTTCAGG	8850
rs190875179	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20115137	CAAACCCAATTATAG[C/T]CTCAGTCGATGGCTA	8850
rs190889930	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20057252	AGTATTGGGATGGAG[A/G]GCAAGCCTTTTTGTA	8850
rs190944795	snp	C/T	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20109122	CTCAGAATGTATTCC[C/T]GTTGTTAAGCAAGAC	8850
rs190948215	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20087322	TACCTCATAAATATG[C/T]ACAATTATATGTTAA	8850
rs190957263	snp	C/T	0.00438332	0.0466095	intron-variant	KAT2B	GRCh38.p7	3:20068530	TAAGTTCCCTGTACT[C/T]ATCCTTTTTTCTTTC	8850
rs190968513	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20056680	AGGAAGAAATGAGTT[C/G]ATAGAAGGTCTTGAA	8850
rs191093601	snp	G/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20075518	AGATGCCAATTGCAA[G/T]TCCCAGGTTATGACC	8850
rs191122516	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20145058	CACCTCGGCCTCCCA[A/G]AGTGCTGGGATTACA	8850
rs191204310	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20084174	GTAGTCATAGCTGTT[C/G]TTGTCTGGCTTTCTT	8850
rs191209666	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20064281	GAAACATGTATACAT[C/T]GTGTAATGGCCAAAT	8850
rs191246626	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20080703	GTAGCCACTAGCCAT[A/G]TGTGGCTATTGAACA	8850
rs191257721	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20141896	TTAATAAAGCACAGC[A/G]GGCTCCTCTCTCTCC	8850
rs191258963	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20062501	TAGTTTTGCTCTGTC[A/C]CCCAGGCTGGAGTGC	8850
rs191266950	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20046678	CTGTTGGCTAAGGGC[C/T]GGTGGGTGGGGCACT	8850
rs191272673	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20113122	CTGTGGAGGGAGATT[C/T]TGAAGCACTTAAACT	8850
rs191326192	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20093148	CCCCAAGAAACAGAC[C/T]CTGAGACAAGGATTT	8850
rs191331663	snp	A/G	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20140849	GTTACCATTTCTACA[A/G]GAGTCATTACTTTTT	8850
rs191346038	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20088797	TGTGCTTTTTGATCA[C/T]ATTCAAAAAATCTTT	8850
rs191346467	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20059476	TAATCCCAGCACTTT[A/G]GGAGGCCGAGGCAGG	8850
rs191358016	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20057436	ATAAGGCACTACTTA[C/T]TTTGCTCATCCTGGT	8850
rs191421567	snp	A/G	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20103927	CTCTGTCCAAGTGTC[A/G]TGACTTTTGTGAGTA	8850
rs191439429	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20064062	TGGGCTATCTATTCT[A/G]TTCCATTAGTATATA	8850
rs191507818	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20060416	AGACCAACCTGACCA[A/T]CAGGGAGAAACCCTG	8850
rs191517987	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20043416	ATTACAGAGAAGTTC[A/G]GAAAAACTACTTTCT	8850
rs191566817	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20111378	CTGTATGATGCTGCA[C/G]AATAAGGTGATTTTA	8850
rs191589740	snp	A/T			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070885	GTGGTGGTGCATGCC[A/T]GTAACCCCAGCTACT	8850
rs191657177	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20130732	AAGGTGGCCAAGCAT[C/G]ACAAACTCAGAAGGA	8850
rs191672030	snp	A/G	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20125046	TATATACATGAGGCC[A/G]GGCGCGGTGGCTCAG	8850
rs191686446	snp	A/C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20083440	TGATTGTCAGTATAG[A/C/T]AAATAGTTTAGCTTT	8850
rs191702723	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20050966	AGCACTTTGAGAGGC[C/T]GAGGTGGGCAGATCG	8850
rs191880040	snp	C/T			utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152567	ACTCACCAAGCAGTG[C/T]GCCTAAAGCAAGGTG	8850
rs191886013	snp	C/T	0	0	intron-variant	KAT2B	GRCh38.p7	3:20080275	TCATTGCATTTTGGC[C/T]ATCAGGCTGCTCCAT	8850
rs191890052	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20100791	TATATATTTTGGTAA[G/T]CTTATTGACTTCAAA	8850
rs191893208	snp	C/G	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20081519	AAGGCAAAGCCTCCC[C/G]TCGTCCCCTCACTTG	8850
rs191900055	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20046230	GTTGCTTGGGTTCTC[A/G]GCAAGGTGCCACATT	8850
rs191900817	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20062658	GTAGAGACGGGGTTT[C/T]GCCTTGTTTGCCAGA	8850
rs191959802	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20061052	TATTAAGAAATTCAC[A/G]TTATTGTGCAATCAT	8850
rs191969012	snp	C/G	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20059202	CAGATCACTTGAGGT[C/G]GGGAGTTCGAGACCA	8850
rs191978829	snp	C/G	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20098983	GCAGTAAGCGAGAAA[C/G]GAGGGAAAGATGTTA	8850
rs192095565	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20131813	AAGAGATCCTCCCTC[C/T]TTGGCCCCCCAAAGT	8850
rs192120930	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20148820	TTGGTGCAAATAGAA[A/G]AACATCAGCTTATCC	8850
rs192135299	snp	A/C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20119461	TTTACTATTTTGATG[A/C/G]CTTGTGGCTTATGTT	8850
rs192141152	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20096155	GTGGCTGTAAGTCCT[A/G]TCTCTAATGCTTTAA	8850
rs192142444	snp	C/G	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20073357	CTGACCATTATAAGT[C/G]GGTGACTTCTTATGC	8850
rs192150038	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20099462	CCTATAGTGGCCTGG[A/T]TGGGCATGTGCCAAG	8850
rs192151902	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20141413	CAGAACTGGGGAGTA[C/T]ACAAAGGCCATTTAT	8850
rs192154572	snp	C/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20078412	TTTTCTTTCTCTTCT[C/G]TCCAGGCTGATGTGC	8850
rs192169588	snp	G/T	0.00358779	0.0422022	intron-variant	KAT2B	GRCh38.p7	3:20111941	TCCCTTTGTGAATCT[G/T]CTTGGGTATTTTCCA	8850
rs192182532	snp	A/T	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20072073	CACTGGGGGCAATGG[A/T]AGCAAAGTGTGTGGG	8850
rs192192056	snp	A/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20138761	TACATTGATTTGTGA[A/G]AACTATTAGTATATA	8850
rs192195062	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20058360	CTCGGGAGGCTGAGG[C/T]AGGAGAATTGCTTGA	8850
rs192195874	snp	C/T	0.030278	0.119257	intron-variant	KAT2B	GRCh38.p7	3:20062390	ATATTATATATAACA[C/T]AATAAATTATATATT	8850
rs192291467	snp	C/G	0.00279162	0.0372561	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038134	GAAAAATAATGTTCA[C/G]TTAATGGCACAAGCC	8850
rs192306508	snp	C/T			utr-variant-5-prime, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20040250	TGGGGGAGCAGCTGC[C/T]GCCGCTGCCGCCGCC	8850
rs192380100	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20117994	TGACAGAGAAATCCT[C/G]TGTATTTTATATGCT	8850
rs192396728	snp	C/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20078033	TACAAAAATCAGCTG[C/G]TGTGGTGGCATGTGC	8850
rs192465068	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20104542	TGATCTTCTCAAAAA[C/T]GGGTAATATTACTGG	8850
rs192510317	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20074107	GAAAAAAAAAATCAC[A/G]TATCCTTTGACCTGG	8850
rs192527525	snp	A/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20125681	GTGTACACATATAAT[A/T]CTCCAATTTCTCAAA	8850
rs192532272	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20058599	CTGATCCCCACCCTG[C/T]ATACTTTCCTCTTTT	8850
rs192624917	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20134452	GCCAGGCTGGAGTGC[A/G]TTGGCGCGATCTCAG	8850
rs192633431	snp	C/G	0.00557542	0.0525036	intron-variant	KAT2B	GRCh38.p7	3:20085697	TGTGTTTTTAGTAGA[C/G]ACAGGGTTTTGCCAC	8850
rs192635397	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20053578	GGAAGGTATATGAGT[A/G]TTATGAGATCAGTGA	8850
rs192641244	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20067528	ATGAAGTTAAGATCT[A/G]TATCTCTAAAACTCT	8850
rs192647471	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20117416	CTGTGATAAATGACA[C/T]TCATAAGGATGAACC	8850
rs192651497	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20054317	TATCTTTAGTAGAGA[C/T]GGGGTTTTACCATCT	8850
rs192712668	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20090887	TGGGACTACAGGCAT[A/G]TGACACCACACCTGC	8850
rs192737615	snp	C/T	1.6498e-05	0.00287206	intron-variant	KAT2B	GRCh38.p7	3:20148318	GAAGGTGGGTGTCCT[C/T]TTTATTCACCTCATG	8850
rs192747064	snp	A/G	0.00026281	0.0114602	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20095398	AACAAGTTTATTTCT[A/G]TCTATTTAAGGTGAG	8850
rs192758413	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20143007	AATACAAGGAATTGG[G/T]GTTGGAGAAGCCAAA	8850
rs192805727	snp	A/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20106583	AAAGCTGAAAAGTAT[A/T]AATTGAGGTCTATAA	8850
rs192814046	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20066654	GATCCTCCCACCTCG[A/G]CATCCCAAAGTGCTG	8850
rs192922739	snp	C/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20128814	GGAGTTTGAGACCAG[C/T]CTGACCAATGTGGTA	8850
rs192935960	snp	C/G	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20081997	TTATATATCATAGCC[C/G]TTCCTCCCCTAAATA	8850
rs192943185	snp	C/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20048503	CCAGATTTAATTCTG[C/T]GGTTGTTAAGTAAAT	8850
rs192966230	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20113721	AGTGAGAGCTGGGAC[C/T]GGCTTCCCAGCACCC	8850
rs192991872	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20048030	GCAATATTGTCACAG[C/T]AAAGTACAAAGCATG	8850
rs193015117	snp	A/T	0.00914312	0.0669923	intron-variant	KAT2B	GRCh38.p7	3:20085201	TGTCTATTAATTTAA[A/T]AAAAAAGTTTATAAG	8850
rs193025624	snp	G/T	0.00597247	0.0543191	intron-variant	KAT2B	GRCh38.p7	3:20054138	TTTTTTGTTTTTTTG[G/T]TTTTTTTTTGAGACG	8850
rs193137963	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20094497	GCAATTACTAATACC[A/G]ACCGCATGGGATTGG	8850
rs193142083	snp	A/T	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20060242	TTCTCTTGGGTAGAT[A/T]CTTAGTGGATTTGCT	8850
rs193154426	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20133810	TACATAAACTGTAAA[C/T]GTATTTGCACGCCGT	8850
rs193162300	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20153844	AACTTGATGTTTTCT[A/G]TCAGCATAAATAAAA	8850
rs193167923	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20101887	CATTCCAGTGTGGCT[A/G]CTAGAAAATTTAAAA	8850
rs193173066	snp	A/G	0.00438332	0.0466095	intron-variant	KAT2B	GRCh38.p7	3:20063092	ATTTATTTTTAGACA[A/G]TATCTTGCTCTGTTT	8850
rs193291573	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20076705	TTAGCAAGTTTCCTA[C/T]ATTTTTTCTTATCTT	8850
rs193296069	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20042352	GCAAGCCCAGGAGTT[C/G]ATCATGAAGGGCATT	8850
rs199507569	in-del	-/AAAT			intron-variant	KAT2B	GRCh38.p7	3:20073724	TTTTAAAAAAATAAA[-/AAAT]TAAATAAAACAGAAC	8850
rs199526564	in-del	-/AT			intron-variant	KAT2B	GRCh38.p7	3:20043742	TTAAAAAAAAAAAAA[-/AT]TTAACTGGACTTGAT	8850
rs199548798	snp	A/C			utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20153937	TGCAAATGGCTATTG[A/C]GTTGGAAGTATTGTT	8850
rs199552217	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20122653	ATTGTTTGCCTTTTA[C/T]TTTGATCATCATAGG	8850
rs199552871	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20144213	GAGAAGGAAACTTTC[A/C]AATTGAAACAGTCTT	8850
rs199564445	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20062587	TTGCCTCAGCTTCCC[C/G]AGTAGCTGGGATTAC	8850
rs199589780	snp	A/G	0.0243677	0.107657	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20072363	AAATGTAATGGCTGG[A/G]AAAACCCTAACCCCT	8850
rs199599035	in-del	-/A	0.0142736	0.0832652	intron-variant	KAT2B	GRCh38.p7	3:20150972	TTAGGTGGAAAAGTG[-/A]AAAGGAATGTAAACA	8850
rs199609220	in-del	-/AA			intron-variant	KAT2B	GRCh38.p7	3:20050200	GTGAGACCCTGTCTC[-/AA]AAAAAAAAAAAAAAG	8850
rs199609549	in-del	-/G			intron-variant	KAT2B	GRCh38.p7	3:20103958	TTCCATGGGTGGTTT[-/G]TATGTAGTTTCTGAC	8850
rs199625680	snp	C/T	3.56132e-05	0.00421963	intron-variant	KAT2B	GRCh38.p7	3:20147933	ACCAAAAGCACTTCT[C/T]ATTCAGTGTTTCACT	8850
rs199626669	in-del	-/A			intron-variant	KAT2B	GRCh38.p7	3:20090609	GGTTTTCTGTTGTGT[-/A]TTTTTGCATCCATGT	8850
rs199633688	in-del	-/C			intron-variant	KAT2B	GRCh38.p7	3:20114532	GATAAATATTAGTAA[-/C]TTTTATGATGGTAAT	8850
rs199649982	in-del	-/TGTGTGTG			intron-variant	KAT2B	GRCh38.p7	3:20121733	ATACACATATGCATA[-/TGTGTGTG]TGTGTGTGTGTGTGT	8850
rs199704153	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20084823	TTCACCTCTATTTCA[A/T]CCAGAGCAACTCCTT	8850
rs199714120	snp	C/T			intron-variant, downstream-variant-500B	KAT2B, MIR3135A	GRCh38.p7	3:20137746	AGGCTGGTCTCGAGC[C/T]CCTGGACTCAAGCAA	8850
rs199733016	in-del	-/AT	0.232359	0.249377	intron-variant	KAT2B	GRCh38.p7	3:20061985	TATTATATATAAAAC[-/AT]ATAATATATAAAACA	8850
rs199840608	in-del	-/A			intron-variant	KAT2B	GRCh38.p7	3:20052673	AAGAAAAAAAAAAAA[-/A]GAGAGAAAAAGAGGC	8850
rs199845091	in-del	-/CTTC	0.0566069	0.158427	intron-variant	KAT2B	GRCh38.p7	3:20130991	ATGTGAGAAACAGTT[-/CTTC]CTTTAGTTTCCTGGC	8850
rs199880019	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20040800	GCGCTCGCCGCTCTC[G/T]GACCGCGGATGGGTG	8850
rs199900176	snp	C/G	1.66128e-05	0.00288204	intron-variant	KAT2B	GRCh38.p7	3:20101491	GATGCAAGTTCTTTT[C/G]CTTTGGCCCCATAAA	8850
rs199916721	snp	C/G	0.000181925	0.00953569	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20114934	AACTCTCCCATCTGG[C/G]ATCAGGATTTTCTCT	8850
rs199925890	snp	A/G	0.0019981	0.0315445	missense, intron-variant, nc-transcript-variant	KAT2B	GRCh38.p7	3:20148461	CAGAAGCTCCAGGAT[A/G]TTATGAAGTTATAAG	8850
rs199926199	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20051059	ACAAAAATTAGCTGG[A/G]CATGGTGGCACACAC	8850
rs199926602	snp	C/T			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070322	TTCTTTTTTTTTTTT[C/T]TGAGATGGAGTCTCG	8850
rs199935186	in-del	-/C			intron-variant	KAT2B	GRCh38.p7	3:20107365	CCCAATATATAAAAA[-/C]ATGCCATTTCAGCTG	8850
rs199977594	in-del	-/T			intron-variant	KAT2B	GRCh38.p7	3:20062418	ATTATATATTATATA[-/T]TATTATATATAATAT	8850
rs199978857	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20092235	TTTATTTATTTATTT[A/T]TTTATTTATTTGAGA	8850
rs199996527	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20144602	CCAGGTTTCTTTTTT[C/T]TTTTTTTTTTTTAAG	8850
rs200001128	in-del	-/TT			intron-variant	KAT2B	GRCh38.p7	3:20144614	TTCTTTTTTTTTTTT[-/TT]AAGATTTGGACTTAT	8850
rs200036073	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20086152	TGGTATGCACCTGTA[A/G]TCCCAGCTATTTGGG	8850
rs200042715	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20073725	TTTTAAAAAAATAAA[A/T]AAATAAAACAGAACG	8850
rs200097819	in-del	-/T			intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20137542	TCCTTTTTTTTTTTT[-/T]GAGACAGGGTCTCAC	8850
rs200121446	in-del	-/T			intron-variant	KAT2B	GRCh38.p7	3:20078892	TTTTTTTTTTTTTTT[-/T]GAGAAGGAGTCTCAC	8850
rs200142541	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20127560	TCAAGGTAAGGGTAA[A/G]CCCAAGGTCTTAGAA	8850
rs200187355	in-del	-/T			intron-variant	KAT2B	GRCh38.p7	3:20073708	TGATTATAATTTACC[-/T]TTTTTAAAAAAATAA	8850
rs200253660	in-del	-/CTG	0.162253	0.234095	intron-variant	KAT2B	GRCh38.p7	3:20054221	TGCAATCTCCGCCTC[-/CTG]GGTTCAAGCAATTCT	8850
rs200264278	snp	A/G	1.65803e-05	0.00287922	intron-variant	KAT2B	GRCh38.p7	3:20148370	CCACATGGAATTTCC[A/G]TATTAGATACCTTAC	8850
rs200282360	snp	C/T	0.000603784	0.0173645	intron-variant	KAT2B	GRCh38.p7	3:20148047	AGTGATTTTTTTTTT[C/T]CCCCACCAAGCAACT	8850
rs200290890	snp	A/T	0.00398564	0.0444627	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20154218	ATTGTCTCTTCTATA[A/T]TGAAAGCATTTTTAT	8850
rs200341228	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20047082	TGTTTTGCCCCCCCC[C/T]TTTTTTTTTCTGAGG	8850
rs200343063	in-del	-/T			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20071009	GAGAGACTCTGTATA[-/T]AAAAAAAAAAAAACC	8850
rs200387198	snp	A/G	1.67377e-05	0.00289284	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20099873	GCAGCTCTTGAGAAA[A/G]TCTATTTTACAAAGA	8850
rs200410446	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20138403	ATACATTTTTGACTA[G/T]GTGTTTCTTGTAGGT	8850
rs200430429	snp	A/C			intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20135654	GCAAGACTCCATCTC[A/C]AAAAAAAAAAAATAA	8850
rs200471371	snp	C/T	0.00036673	0.0135363	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20126113	GGCTCGTCTTTGACC[C/T]GTAAGTGGTACTTTC	8850
rs200480938	snp	A/T	8.5274e-05	0.00652915	intron-variant	KAT2B	GRCh38.p7	3:20114852	ACAGTAGTTTTTTTT[A/T]AATCTTATTGCTATT	8850
rs200481068	in-del	-/C	0.0170251	0.090679	intron-variant	KAT2B	GRCh38.p7	3:20134026	TATGTTGCAACTACA[-/C]CCCCCCCTCACTTGT	8850
rs200483308	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20146670	TAATATCCACCACTT[A/T]ATGAGTCTGCCATTT	8850
rs200539117	in-del	-/T	0.00953873	0.0683987	intron-variant	KAT2B	GRCh38.p7	3:20076791	GAATTCTGTTAGGAA[-/T]TACGCAAGCCTGAAT	8850
rs200540757	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20139217	ACTGCACCCAGCCAG[A/T]CTTCTTTTTTTTTAA	8850
rs200560854	snp	A/C/G	0.000230691	0.0107377	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20072391	CCTCACCCACTCCCC[A/C/G]CAGAGCCGACCTGCA	8850
rs200572213	snp	C/T	0.00199795	0.0315434	intron-variant	KAT2B	GRCh38.p7	3:20099836	TTAAGTTTTTCTTTT[C/T]CTTTTTTTTAATGAT	8850
rs200572606	snp	A/G	4.94246e-05	0.0049709	missense, intron-variant, nc-transcript-variant	KAT2B	GRCh38.p7	3:20127482	GTGGTATCTGTTTCC[A/G]TATGTTCCCATCTCA	8850
rs200586455	in-del	-/AC	0.0644693	0.167566	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039539	TTTCAAACAAAAATT[-/AC]AGAGAATAGTAAGTT	8850
rs200599320	in-del	-/TG			intron-variant	KAT2B	GRCh38.p7	3:20106978	ATATATATATATATA[-/TG]TATATATATATATAT	8850
rs200629500	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20140755	CCTCGGCCTCCCAAA[G/T]TGTTGGGATTACAGG	8850
rs200632861	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20085640	CTCAGCCTCCCGAGT[C/T]GCTGGGACTACTGGC	8850
rs200656305	in-del	-/C			intron-variant	KAT2B	GRCh38.p7	3:20144207	GTGAAGAGAAGGAAA[-/C]CTTTCAAATTGAAAC	8850
rs200681006	snp	A/G	1.65217e-05	0.00287412	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20146356	AACAGGCACAAATTC[A/G]AAAAGTTTACCCTGG	8850
rs200701344	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20117109	GAAAACTCCCCTTGA[C/G]CCTTGTTTGCTCAAA	8850
rs200703876	in-del	-/TATATATATGTA	0.0287284	0.116357	intron-variant	KAT2B	GRCh38.p7	3:20078694	TTTCTGATATATGTG[-/TATATATATGTA]TATATATATGTACAC	8850
rs200723262	snp	C/G/T	0.00676609	0.0577691	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20040629	CCGGGGGCTCGGGCG[C/G/T]CTGCGGTCCGGCGAC	8850
rs200767274	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20065105	ATCGGTTGCATACTA[C/T]TGACCTCTAACCCTG	8850
rs200787456	in-del	-/ATA	0.0448719	0.142907	intron-variant	KAT2B	GRCh38.p7	3:20087417	ATATATTTATCGTGT[-/ATA]ATGTGATATTTTGAG	8850
rs200804615	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20104890	TTTTGTTGTTTTTTT[G/T]TTTTTTTTTTTTTTG	8850
rs200818598	in-del	-/G			intron-variant	KAT2B	GRCh38.p7	3:20139808	TCACTTTATTTTTTT[-/G]ACCATCTTTTCTTTG	8850
rs200876395	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20138523	TGTTGCTAAATATTT[A/T]AAAAATTTCCATTTT	8850
rs200876804	snp	A/C/T	0.000179223	0.00946474	intron-variant	KAT2B	GRCh38.p7	3:20122635	TTGTGTTTAGAACCA[A/C/T]CCATTGTTTGCCTTT	8850
rs200900685	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20138399	ACCAATACATTTTTG[A/T]CTAGGTGTTTCTTGT	8850
rs200909539	in-del	-/G			intron-variant	KAT2B	GRCh38.p7	3:20151440	TTGGTAGTCAGAAGT[-/G]GGGTTTTTTTTTTCC	8850
rs200913277	in-del	-/AT	0.0119091	0.0762411	intron-variant	KAT2B	GRCh38.p7	3:20134907	TCTAAAATTATTGTC[-/AT]ATCAACATGTAATAA	8850
rs200915849	snp	C/T	1.71091e-05	0.00292476	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152542	TTTTTTTCCCCTCTG[C/T]TTCTTAGAAACTCAC	8850
rs200920992	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20126577	CCTGTAATCCCAGCA[C/T]TTTGGGAGGCTGAGG	8850
rs200923352	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20128496	AGCAACAAAAAAAAA[A/C]AAAACAAAACAAAAA	8850
rs201015820	snp	A/C/T	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20086150	GATGGTATGCACCTG[A/C/T]AGTCCCAGCTATTTG	8850
rs201018750	snp	C/T	0.00011844	0.00769455	intron-variant	KAT2B	GRCh38.p7	3:20146475	ATTTTTTAGTAATGC[C/T]GTGGTTTGTGTTTGA	8850
rs201047416	in-del	-/C	0.00874735	0.0655527	intron-variant	KAT2B	GRCh38.p7	3:20073179	AGTTTTTCCTAGATA[-/C]TAAAATTTCAGTCCA	8850
rs201056968	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20072309	TGTTAAATAATTTTG[C/T]CTCTTTCTTTATTCC	8850
rs201066836	snp	A/C/T	1.69934e-05	0.00291486	stop-gained, synonymous-codon, intron-variant, nc-transcript-variant	KAT2B	GRCh38.p7	3:20148462	AGAAGCTCCAGGATA[A/C/T]TATGAAGTTATAAGG	8850
rs201070925	in-del	-/C			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070312	TTTCTTTCTTTCTTT[-/C]TTTTTTTTTTTGAGA	8850
rs201093573	in-del	-/AGAG			intron-variant	KAT2B	GRCh38.p7	3:20096950	AAAGAATAATAGGAA[-/AGAG]AGAGAGAGAGAGAGA	8850
rs201184924	in-del	-/T			intron-variant	KAT2B	GRCh38.p7	3:20073725	TTTTAAAAAAATAAA[-/T]AAATAAAACAGAACG	8850
rs201274748	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20092236	TTATTTATTTATTTA[A/T]TTATTTATTTGAGAT	8850
rs201288517	in-del	-/TTA			intron-variant	KAT2B	GRCh38.p7	3:20146667	GTTAATATCCACCAC[-/TTA]TTAATGAGTCTGCCA	8850
rs201299792	snp	A/C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20104194	CCTCCTGAGCCAACA[A/C/G]CTGAAGGCAAAAAGT	8850
rs201328564	snp	A/G/T	0.000338918	0.0130138	intron-variant	KAT2B	GRCh38.p7	3:20146476	TTTTTTAGTAATGCC[A/G/T]TGGTTTGTGTTTGAA	8850
rs201337657	in-del	-/CCTT	0.00478085	0.0486577	intron-variant	KAT2B	GRCh38.p7	3:20124857	TGTCACCAGTTAGGG[-/CCTT]CCTTCCTTGAAGAGC	8850
rs201350372	in-del	-/TA			intron-variant	KAT2B	GRCh38.p7	3:20043728	CAGATTTGCTTTTTT[-/TA]AAAAAAAAAAAAATT	8850
rs201353871	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20086151	ATGGTATGCACCTGT[A/C]GTCCCAGCTATTTGG	8850
rs201384802	in-del	-/CA			intron-variant	KAT2B	GRCh38.p7	3:20106460	ACACACACACACACA[-/CA]CACATTCTGTCTCTC	8850
rs201390030	in-del	-/C	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20130678	CCCAGAAAGGCAATT[-/C]CCCCCCCATAACCAT	8850
rs201397595	snp	A/C	3.29739e-05	0.00406028	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20101430	AAGACTGCGATCTCC[A/C]AATGATGATATTTCT	8850
rs201414195	in-del	-/G			intron-variant	KAT2B	GRCh38.p7	3:20083254	TTATTTTATTTTTTA[-/G]TTTTTAATAATATGC	8850
rs201416372	in-del	-/A			intron-variant	KAT2B	GRCh38.p7	3:20078286	GGAATTTCTATTGTT[-/A]TTTTGGAGTCCATTG	8850
rs201528219	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20144212	AGAGAAGGAAACTTT[C/T]AAATTGAAACAGTCT	8850
rs201537605	snp	C/T	0.00199803	0.031544	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20126034	AAGATCCTGATGTGG[C/T]TGGTTGGCCTACAGA	8850
rs201620133	snp	C/G/T			intron-variant	KAT2B	GRCh38.p7	3:20062578	GCGATTCTCTTGCCT[C/G/T]AGCTTCCCGAGTAGC	8850
rs201646712	in-del	-/T/TT			intron-variant	KAT2B	GRCh38.p7	3:20141800	CTTTTTTTTTTTTTT[-/T/TT]GGAAAATACAAACAA	8850
rs201653182	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20144600	AGCCAGGTTTCTTTT[C/T]TCTTTTTTTTTTTTA	8850
rs201659919	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20141370	AATTTTCTAAGGCAG[A/G]AAAAAAAAACACTCA	8850
rs201663437	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20148359	GAAATGATTTCCCAC[A/G]TGGAATTTCCATATT	8850
rs201721343	in-del	-/AT	0.109289	0.20664	intron-variant	KAT2B	GRCh38.p7	3:20061939	TATCATATATAAAAC[-/AT]AATATATATTATATA	8850
rs201725321	in-del	-/AG			intron-variant	KAT2B	GRCh38.p7	3:20069092	GTCAGTCAGACTAAC[-/AG]AATACATTAACAAGA	8850
rs201795949	snp	C/G	1.65362e-05	0.00287538	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20101323	TACAAATTTAGTCAC[C/G]TGCCAGCAAAAGAAA	8850
rs201810024	snp	A/G	0.0095476	0.0684298	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20040662	CAGTGGCTGCAGCGG[A/G]CACGGCCGAAGGACC	8850
rs201811492	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20145517	TTTTTCCAAAATTTC[A/G]TTATGATATGTTTAA	8850
rs201815130	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20126821	AGCGAAACTCCATTT[A/C]AAAAAAAAAAAAAAA	8850
rs201828177	in-del	-/A			intron-variant	KAT2B	GRCh38.p7	3:20087943	CATACCTAGCTAATT[-/A]AAAAAAAAATTTTTT	8850
rs201839892	snp	A/G	3.30497e-05	0.00406494	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20122757	ATGGAATTAATCAAC[A/G]AGGTTATGTCTACCA	8850
rs201855469	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20072302	GGCTGCCTGTTAAAT[A/G]ATTTTGTCTCTTTCT	8850
rs201895705	in-del	-/A			intron-variant	KAT2B	GRCh38.p7	3:20096474	AGAAGGAATAACCTT[-/A]AAAAAAAATAAACCT	8850
rs201896750	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20138400	CCAATACATTTTTGA[C/T]TAGGTGTTTCTTGTA	8850
rs201896939	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20091687	AGTTTTGGTATATTG[C/T]ATTTCCACTTCTGTT	8850
rs201910873	snp	C/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20057847	CTGCCAAGGGGGTTC[C/T]AGACCTTTCAGTCAG	8850
rs201915994	snp	G/T	1.73601e-05	0.00294614	intron-variant	KAT2B	GRCh38.p7	3:20148033	AGGATGTTAATGGAA[G/T]TGATTTTTTTTTTTC	8850
rs201922668	snp	C/T	3.29592e-05	0.00405938	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20072398	CACTCCCCCCAGAGC[C/T]GACCTGCAGCAAATA	8850
rs201923590	in-del	-/T			intron-variant	KAT2B	GRCh38.p7	3:20144801	TCTTTTTTTTTTTTT[-/T]AAGAGGAAGTCTCGC	8850
rs201929856	in-del	-/CTC	0.0189856	0.0955633	intron-variant	KAT2B	GRCh38.p7	3:20113538	CTGCCTTCTTTTCTT[-/CTC]TATTACTAATGGTGG	8850
rs201934698	in-del	-/T			intron-variant	KAT2B	GRCh38.p7	3:20066746	ACCCACTGCACCGCA[-/T]TTAAAAAAAAAAAAT	8850
rs201990785	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20089462	CTGGAGTGCAATGGC[A/G]CAATCTCAGCTCACT	8850
rs202027627	in-del	-/A			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20071007	AGAGAGACTCTGTAT[-/A]ATAAAAAAAAAAAAA	8850
rs202085432	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20096973	AGAGAGAGAGAGAGA[A/G]AGAGAGTGGGGGAAG	8850
rs202106321	in-del	-/A			intron-variant	KAT2B	GRCh38.p7	3:20118727	GCGAAACTTTGTCTC[-/A]AAAAAAAAAAAAAAA	8850
rs202108631	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20141801	CTTTTTTTTTTTTTT[A/C]GAAAATACAAACAAC	8850
rs202109420	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20129030	AAAAAAAAAAAAAAA[C/T]AATGTTATTCATTTA	8850
rs202116411	snp	C/T	1.64928e-05	0.00287161	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20148261	AGAGCCCAGAGACCC[C/T]GACCAGCTTTACAGC	8850
rs202116607	in-del	-/A			intron-variant	KAT2B	GRCh38.p7	3:20138373	TTGTTGTAGAAATAG[-/A]AAAATATTTAACCAA	8850
rs202132144	snp	A/G	6.64684e-05	0.00576453	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20111760	TGCCTCTTGAAAAAC[A/G]AACTCTAATCCTCAC	8850
rs202164686	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20092243	TTTATTTATTTATTT[A/T]TTTGAGATGGAGTGT	8850
rs202165300	in-del	-/GGAC/GGACT			intron-variant	KAT2B	GRCh38.p7	3:20086149	GATGGTATGCACCTG[-/GGAC/GGACT]TAGTCCCAGCTATTT	8850
rs202184633	in-del	-/C			intron-variant	KAT2B	GRCh38.p7	3:20144285	GGATTCTTTTTTTTT[-/C]TTTTTTTTTTTTTTT	8850
rs202211242	in-del	-/AT			intron-variant	KAT2B	GRCh38.p7	3:20062465	TATATATATATATAT[-/AT]TAGAGGTAGTTTTGC	8850
rs367597536	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20142316	TGAATGGGTGATGGA[A/G]GTTTGGAGATCTTAA	8850
rs367597587	in-del	-/GTT			intron-variant	KAT2B	GRCh38.p7	3:20089847	TTTTGATAGTTTGTT[-/GTT]AGTATACAGAAACAT	8850
rs367606955	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20054971	GGAGACAGATATTAA[A/G]TGAAAGAAAAATTAA	8850
rs367647970	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20061957	ATATATATTATATAT[A/G]AAACATAATATATAT	8850
rs367655662	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20049629	AGGCATTCTGCTGTC[A/G]TTTGAAATTTATTGT	8850
rs367719673	snp	G/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20097642	CCTGAGTTCAAGTGA[G/T]TCTCCTGCCTCAGCC	8850
rs367786973	snp	C/T	0.000181481	0.00952404	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20126010	TCCCTCAACCAGAAA[C/T]CAAACAAGAAGATCC	8850
rs367805432	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20100449	GAAGCCGTTTTACTC[A/G]GGGAATCTGTTAAAA	8850
rs367834653	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20095486	GCCAGGTCGTGGCTG[G/T]GAAGGCTTTCAGCTC	8850
rs367883436	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20102931	CAGATAACATGGAAG[A/T]ATTGTATAATTTAAA	8850
rs367969548	in-del	-/ATATA	0.15665	0.231917	intron-variant	KAT2B	GRCh38.p7	3:20061867	TAATATACATAAAAT[-/ATATA]ATATATTTGTATAAA	8850
rs367987625	snp	C/T	3.30896e-05	0.00406739	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20095280	GCTCATGTTTCCCAC[C/T]TGGAGAATGTGTCAG	8850
rs367991012	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20052583	ATGGTGGCTCATGCC[C/T]GTAATCCCAGCACTT	8850
rs367997029	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20077159	TCAAGTAGAAAGAAC[A/G]TTCAGTTGGGAACTA	8850
rs368016653	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070134	GATGCTGATGTAGGT[G/T]CTTCTCCTGGCCCTG	8850
rs368108314	in-del	-/T			intron-variant	KAT2B	GRCh38.p7	3:20146672	ATATCCACCACTTAA[-/T]GAGTCTGCCATTTGT	8850
rs368125825	in-del	-/A			intron-variant	KAT2B	GRCh38.p7	3:20092802	GCCTCCTGGGTTCAA[-/A]GCAATTCTCCTGCCT	8850
rs368153924	in-del	-/TA			intron-variant	KAT2B	GRCh38.p7	3:20062037	AAACATAATATATAT[-/TA]TATATAAAACATATA	8850
rs368168370	in-del	-/AGA			intron-variant	KAT2B	GRCh38.p7	3:20124871	GCCTTCCTTCCTTGA[-/AGA]GCTGTTTGTGGAGCA	8850
rs368172380	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20132251	TGGTGGTGCATGCCT[A/G]TAATCCCAGCTACTC	8850
rs368180203	in-del	-/ATTCTTTTTTTTT			intron-variant	KAT2B	GRCh38.p7	3:20144273	GAGATTGCCCTTGGG[-/ATTCTTTTTTTTT]TTTTTTTTTTTTTTT	8850
rs368232090	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20066622	CAGGCTGGTCTCGAA[C/T]TCCTGACCTCATGTG	8850
rs368241341	snp	C/T	0.000153988	0.00877328	missense, intron-variant, nc-transcript-variant	KAT2B	GRCh38.p7	3:20127491	GTTTCCGTATGTTCC[C/T]ATCTCAAGGATTCAC	8850
rs368287383	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20058783	AAGGATTACTGAACC[A/G]TTTAATCTGTATATG	8850
rs368313257	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20053594	TTATGAGATCAGTGA[A/G]TTAAAAGCTACAAAG	8850
rs368327662	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20086188	GAGGTGGGAGGATTA[A/C]CTGAGCCCAGAAAAG	8850
rs368387985	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20088682	AAAATGTTCTCTTCC[A/G]TTCCATAGGTTGTCT	8850
rs368389160	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20061913	ATATTATATATAAAA[C/T]ATGTATTATATATCA	8850
rs368442132	snp	C/G/T	0.000117436	0.00766197	intron-variant	KAT2B	GRCh38.p7	3:20040812	CTCGGACCGCGGATG[C/G/T]GTGCTAGGGGCCCAG	8850
rs368458245	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20045302	GGATTACAGGTGTGA[A/G]CCACTGCACCTGGCC	8850
rs368471482	snp	A/C/G	1.84561e-05	0.00303772	intron-variant	KAT2B	GRCh38.p7	3:20148537	AAACTCTGGATGGCG[A/C/G]TGTGGGGGACAAATG	8850
rs368494816	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20041161	GCAAGGAAAAATCTT[C/T]TGGGGGACTGAGTGG	8850
rs368504351	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20088343	ATCCATATGGTTTAC[C/T]ATACTGGCTGTACTA	8850
rs368507599	snp	A/G	0.00438332	0.0466095	intron-variant	KAT2B	GRCh38.p7	3:20055257	TGTGGAGACAGTGAT[A/G]TATGTCAACTTTTTC	8850
rs368523401	in-del	-/T			intron-variant	KAT2B	GRCh38.p7	3:20062198	TATATAAAATATATA[-/T]ATTTTATATAAAATA	8850
rs368600802	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20083689	TATAGTAGGTTTGAC[A/G]TTCCAATGGAAGAAA	8850
rs368635967	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20131619	GTTGCCCAGGCTGGA[A/G]TGCAGTGGCATGATC	8850
rs368666068	snp	C/T	1.71613e-05	0.00292923	intron-variant	KAT2B	GRCh38.p7	3:20122665	TTATTTTGATCATCA[C/T]AGGAGAAAAGAGGAA	8850
rs368688821	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20061989	ATATATAAAACATAT[A/T]ATATATAAAACATAT	8850
rs368758501	snp	C/G	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20083560	TTCTGGTCAGCATCC[C/G]CAAAGAGCCAGGAGT	8850
rs368767930	in-del	-/CAAG			utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152576	GCAGTGTGCCTAAAG[-/CAAG]GTGGTTTAGTTTTTT	8850
rs368772080	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20128676	TGTTCTACTTTCTTG[A/C]TTTTAAGAAAAGGGA	8850
rs368773280	snp	A/C/T			intron-variant	KAT2B	GRCh38.p7	3:20142012	TTAGAGGCTGCTGGC[A/C/T]AACTAAAGCCATCAC	8850
rs368789750	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20042966	GTGCAGTGGCATGAT[C/T]GTAGCTCACTGCAGA	8850
rs368794227	in-del	-/AT			intron-variant	KAT2B	GRCh38.p7	3:20062254	TATATAATATATAAA[-/AT]ATATGATATATAATA	8850
rs368855701	in-del	-/TTATTTA/TTATTTATTTATTTA	0.465263	0.127129	intron-variant	KAT2B	GRCh38.p7	3:20092236	TATTTATTTATTTAT[-/TTATTTA/TTATTTATTTATTTA]TTATTTATTTGAGAT	8850
rs368865284	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20144276	ATTGCCCTTGGGATT[C/T]TTTTTTTTTTTTTTT	8850
rs368877446	in-del	-/T	0	0	intron-variant	KAT2B	GRCh38.p7	3:20058475	GCATCTCTGAAAACC[-/T]TTTTTTTTTTTTTTT	8850
rs368919421	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20115510	GATGCAAAATTTTGA[C/T]GTCAAGAGTTTTTTG	8850
rs368992019	snp	C/T	1.72225e-05	0.00293444	intron-variant	KAT2B	GRCh38.p7	3:20148028	GCAAGAGGATGTTAA[C/T]GGAAGTGATTTTTTT	8850
rs368993475	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20062289	ATATATAAAATATAA[A/T]ATATAATATATAAAA	8850
rs368995146	in-del	-/ATAT			intron-variant	KAT2B	GRCh38.p7	3:20121730	TACATACACATATGC[-/ATAT]GTGTGTGTGTGTGTG	8850
rs369007231	in-del	-/TAT	0.00398564	0.0444627	intron-variant	KAT2B	GRCh38.p7	3:20066824	CTGAATATTTCAAAA[-/TAT]TATTATAATATGTAA	8850
rs369026560	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20110781	TTTCTAAATTAGATG[A/G]CCTGTATTGTCAGTG	8850
rs369046076	snp	A/G	0.000118631	0.00770074	intron-variant	KAT2B	GRCh38.p7	3:20140196	GTGTATGGTGTTCAT[A/G]TGAATGAATTTACTT	8850
rs369060702	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20148624	TGGGATTCCATGCAC[A/C]GTGGCGGGTCAGTGA	8850
rs369149916	snp	A/G	0.000437904	0.0147905	intron-variant	KAT2B	GRCh38.p7	3:20148179	AGAATGAGCTGAATA[A/G]TAATCAGCTGGCAAT	8850
rs369178259	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20123556	TTATTATCTGGCTTT[G/T]CACTGAAAAGTTTGC	8850
rs369188611	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20067709	AGACAGGGTCTCACT[C/G]TGTCACCCAGGCTGG	8850
rs369191003	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20106369	GTGCTCATGCACGTC[C/T]GTTTCCTTCTTTCTG	8850
rs369196715	snp	C/T	0.000149272	0.00863793	intron-variant	KAT2B	GRCh38.p7	3:20127594	GAGCAGAATGTGGGG[C/T]TTCTCACTAAGGCCT	8850
rs369219226	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20141748	TACTTAAAGTGGCTC[A/C]GTCTTGTTCTTGTGT	8850
rs369264551	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20045040	ATTTTTTTGAGACAG[A/G]GTCTCGCTCTGTCAC	8850
rs369327692	snp	A/G/T			intron-variant	KAT2B	GRCh38.p7	3:20107180	GGATTACAGGCATGC[A/G/T]CCACCACAGCTGGCT	8850
rs369368393	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20110436	AGCACTTTGGGAAGC[C/T]GAGGTGGGTGGATCT	8850
rs369378253	in-del	-/TATAT			intron-variant	KAT2B	GRCh38.p7	3:20062309	ATATATAAAATATAA[-/TATAT]TATATATAAAATATT	8850
rs369438321	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20084586	GTAATAAATAAATAA[A/T]TAATTAATAAATGCA	8850
rs369438366	snp	A/C	0.000251714	0.0112158	intron-variant	KAT2B	GRCh38.p7	3:20101284	GCCTTCCCTCTTTTT[A/C]AGGGTGTGAATAACT	8850
rs369445086	snp	C/T	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20109822	TTTCAGTATTGTAAA[C/T]ATAAACAACATTTGG	8850
rs369486690	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20111172	CAGTAACTCCAGTTA[C/T]ACTATGCATTTTATA	8850
rs369529400	in-del	-/TT			intron-variant	KAT2B	GRCh38.p7	3:20085195	CTCTATGTCTATTAA[-/TT]TTTAAAAAAAAAGTT	8850
rs369549515	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20054802	ATAATGAAGTGAGTC[A/T]TGTAACCCAGGATTG	8850
rs369566336	snp	A/G	0.000622283	0.0176282	intron-variant	KAT2B	GRCh38.p7	3:20095227	GTTTGGTTTCCAATT[A/G]AGGTCTTACATATGT	8850
rs369580902	in-del	-/T			intron-variant	KAT2B	GRCh38.p7	3:20133901	TCTTATATTTACTGG[-/T]AATATTTATTCTTGT	8850
rs369624769	snp	C/G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20050367	ATTTTTACATGTGTA[C/G/T]ACATCTATGCAACTG	8850
rs369627172	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20081289	TGGCTGACTGTCTTC[A/C]CGAGAAGTGCAGGCC	8850
rs369627338	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20064503	GAAGTTACGGTTTTG[A/G]TCCTTGACATTTAAA	8850
rs369652846	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20062217	TTATATAAAATATAT[A/T]ATATATAAAAATATA	8850
rs369655034	snp	A/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20090026	GAAAAAAAAAAACGA[A/T]TGGTACTGATCTTTG	8850
rs369657378	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20126402	TAACACTAAGATGTT[C/G]TGCTTTCTTCATAAT	8850
rs369657764	in-del	-/CAAAGA			intron-variant	KAT2B	GRCh38.p7	3:20125819	TGTATCTTATTAGAA[-/CAAAGA]TGAGAAGCTTGGATG	8850
rs369696915	snp	A/G	1.65817e-05	0.00287933	intron-variant	KAT2B	GRCh38.p7	3:20119742	AGCTCTTAAGAGGGG[A/G]TAAGAGAGGGCTGTG	8850
rs369812781	snp	A/C	0.00041266	0.0143583	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20119707	CAAAGCCTCTTCTGG[A/C]CTTGAGGCAAACCCA	8850
rs369812859	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20151005	TACTTTTACTTAGGG[C/G]CAATTTCATTGTTTT	8850
rs369824634	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20133078	AGACATATACAAATG[C/T]GTTTTCAGATAAAAC	8850
rs369870384	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20101744	TTGAGATTTCTATGA[A/T]TGTACCAAAAAGGAG	8850
rs369886691	in-del	-/GTTTT			intron-variant	KAT2B	GRCh38.p7	3:20128496	TTTTTGTTTTGTTTT[-/GTTTT]TTTTTGTTGCTAATT	8850
rs369891339	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20075206	GAGGCGGAGGTTGTA[A/G]TGAGCCGAGATTGCA	8850
rs369891470	snp	C/G	3.29897e-05	0.00406125	intron-variant	KAT2B	GRCh38.p7	3:20148316	GTGAAGGTGGGTGTC[C/G]TCTTTATTCACCTCA	8850
rs369929349	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20130384	TTTATCATTATTCTC[C/T]GCTAGCCAAAGTGAC	8850
rs369942583	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20105240	ATATACTCCCAGGAG[C/T]AATTGTGGTTATAGA	8850
rs369993926	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20145545	TAATTTCCGGATGGG[A/T]TTTTTTTAGTTTTTT	8850
rs370017886	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20053271	GCTCACGCCTGTAAT[A/C]CCAGGTGTGGGATCC	8850
rs370021883	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20147908	AAGTATTAACTATGT[C/T]ATTCTCTTGACCAAA	8850
rs370027230	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20088943	ATAAGGGTCTAATTT[C/T]ATTCTTTTGCATGTG	8850
rs370028173	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20067557	CTGTGTTGTCTTCTC[C/T]AAGAATTTAAAGCTT	8850
rs370033994	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20078109	GCCTGAGCCTGGGAG[A/G]CAGAGGTTTCAGTGG	8850
rs370050105	in-del	-/T			intron-variant	KAT2B	GRCh38.p7	3:20120224	ATTCTTTTTTTTTTT[-/T]CCTTTTCTTTTCTTT	8850
rs370087896	in-del	-/TTTTTTTTTTTTTTT	0.0134861	0.0810011	intron-variant	KAT2B	GRCh38.p7	3:20063535	TTCTGAGTAGGCCTC[-/TTTTTTTTTTTTTTT]TTTTTTTTTTTTTTT	8850
rs370093010	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20149138	TGATTAATTGAATCA[A/T]TTGAGGTCGCTCAAA	8850
rs370110681	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20084558	CTGAGGAGAGATCAC[A/G]TATTGCATTATGGTA	8850
rs370187369	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20108215	TGTGTTTAATGGGAA[A/G]ACATTTTACACTGTT	8850
rs370194153	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20094262	GGCAGCAGGAGAGAG[A/C]GAGCGAGCGAGCGAG	8850
rs370222348	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20100020	CTTTTAATCCTCCTT[G/T]TATATCTCTATCTAC	8850
rs370252243	snp	G/T	0.00953873	0.0683987	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038713	CTGCTTTGCGGAGAA[G/T]GGCAAAAATCTGCGA	8850
rs370255992	snp	C/T	6.2965e-05	0.00561057	intron-variant	KAT2B	GRCh38.p7	3:20152299	GTGTTTAAAGGGAGT[C/T]AAAGATTGCTAATAT	8850
rs370258989	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20067894	TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA	8850
rs370283187	in-del	-/ATATATATT	0.17654	0.238964	intron-variant	KAT2B	GRCh38.p7	3:20062006	TATATAAAACATATA[-/ATATATATT]ATATATAAAACATAA	8850
rs370344547	snp	C/T	1.70061e-05	0.00291595	intron-variant	KAT2B	GRCh38.p7	3:20111591	CTTGACTTCTCTTGT[C/T]ACAGGTGGCTGTGTT	8850
rs370369827	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20054625	TGTGCAGCTTTTTGC[A/G]AGGTTTGTGTGGTAT	8850
rs370374562	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20061918	ATATATAAAATATGT[A/G]TTATATATCATATAT	8850
rs370378388	snp	C/T	0.00398564	0.0444627	intron-variant	KAT2B	GRCh38.p7	3:20062704	TGAGCTCAGGTGATC[C/T]ACCTGCCTCAGCCTC	8850
rs370382348	snp	C/T	1.65781e-05	0.00287902	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20146422	CTATAGAAAGCATTC[C/T]TGGAATTAGTACGTA	8850
rs370405641	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20086058	GATGGATCGCTTGAG[C/G]TCAGAAGTTCGAGAC	8850
rs370407598	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20106183	TTACAAATCATCATC[A/G]TGATGTGAAAAATCT	8850
rs370436695	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20060620	ACAAACAAACAAACA[A/C]ACAAACAACAAACTG	8850
rs370458547	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20054038	CCTGACCTCAAGTGA[C/T]CCATCCTCCTCGGCC	8850
rs370663537	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20108457	ATTTTTAAAATTTAG[G/T]ATCTGCATAACAACA	8850
rs370663586	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20083279	ATATGCTCCTAGACT[C/T]ATAAATAATAGAGGC	8850
rs370668916	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20117331	TTCTACTGTAATTGC[A/G]ATGTGTTCTCTTGGG	8850
rs370678850	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20073724	TTTTTAAAAAAATAA[A/T]TAAATAAAACAGAAC	8850
rs370697779	snp	A/G	0.00914312	0.0669923	intron-variant	KAT2B	GRCh38.p7	3:20147368	TTTGTTTTTTTTTTT[A/G]TACATTAACTACTCT	8850
rs370723532	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20115957	TCATCTGAACCTCAA[A/G]TTTAGGTGTAAATAT	8850
rs370743946	in-del	-/GT			intron-variant	KAT2B	GRCh38.p7	3:20114065	GGGACTTAGGTATCT[-/GT]ATTTCTTTTCTCTTT	8850
rs370748849	snp	C/G/T			intron-variant	KAT2B	GRCh38.p7	3:20112957	GTTTAACCCAAATCC[C/G/T]AAACCTTAGATAGAT	8850
rs370764509	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20051326	TGCATGTGGGCTGAT[A/G]ATGTCACTGCTGGTA	8850
rs370902258	snp	C/T			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070458	TACAGGCGCCTGCCA[C/T]CACGCCCGGCTAATT	8850
rs370959965	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20051774	ATATATGATGAGCTC[A/G]TTATTTAATGGCTGA	8850
rs371009552	in-del	-/A	0.498133	0.030494	intron-variant	KAT2B	GRCh38.p7	3:20073725	TTTAAAAAAATAAAT[-/A]AAATAAAACAGAACG	8850
rs371030771	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20102750	CATCCATTCTTTTCA[A/G]CTTTTTTATAACTTT	8850
rs371034791	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20086233	AGCCATAATTGTGCC[A/G]CTACAATCCAGCCTG	8850
rs371046808	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20131778	TGTGTTGCCCAGGCT[A/G]GTCTTGAACTCCTGG	8850
rs371071253	snp	C/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20144387	TCTGCCTCCTGGGTT[C/T]GCACCATTCTCCTTC	8850
rs371108839	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20074617	ATATACTCTGTCTAG[C/T]TTAAATAAGAAAACA	8850
rs371113392	snp	C/T			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039089	ATCTGATAATAAGCA[C/T]ATTATGACCCACATT	8850
rs371207195	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20151610	CTGACAGTGAGGATT[G/T]AAGAAACCCTACTTT	8850
rs371270987	snp	G/T	0.00438332	0.0466095	intron-variant	KAT2B	GRCh38.p7	3:20074824	GGATTTAAATACCCT[G/T]TGGAGGAGCTTGTGC	8850
rs371278706	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20089230	TTATGTAGTTCTGTA[A/C]AGATTTTAAGATTAT	8850
rs371292271	multinucleotide-polymorphism	AA/TT	0.5	0	intron-variant	KAT2B	GRCh38.p7	3:20085199	TATGTCTATTAATTT[AA/TT]AAAAAAAGTTTATAA	8850
rs371334162	snp	C/T	0.00014843	0.00861354	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20119668	CCTTGAGCAGCCAAA[C/T]GCAGGGAGCAGCAGT	8850
rs371398561	snp	A/G			intron-variant, downstream-variant-500B	KAT2B, MIR3135A	GRCh38.p7	3:20138101	TCTGACTATAAAAGT[A/G]ATGTGTAATCATTGT	8850
rs371422367	in-del	-/T			intron-variant	KAT2B	GRCh38.p7	3:20098533	TAAGAACTTTTTTTT[-/T]ATATGCACACTTATC	8850
rs371492340	in-del	-/TA			intron-variant	KAT2B	GRCh38.p7	3:20078704	ATGTGTATATATATG[-/TA]TATATATATGTACAC	8850
rs371518186	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20144588	GCCACCAAGCCCAGC[C/T]AGGTTTCTTTTTTCT	8850
rs371548043	snp	C/T	0.000240686	0.0109675	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20040695	GAGGCGGTGGCTCGG[C/T]CCGAATCGCCGTGAA	8850
rs371594734	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20046305	AAAAAATAGGCCCAG[A/G]GCATGGTGGCTTGTG	8850
rs371611191	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20100645	GTCAGTTTTCAGTAA[A/G]TTTTATTTTGCCTCC	8850
rs371635657	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20052697	AAGAGGCCGGGCACG[C/G]TGGCTCATGCCTGTA	8850
rs371770350	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20077362	AAAACAAAACCAAGA[A/G]AAGAATTCTAGCTTG	8850
rs371775631	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20092253	TATTTATTTGAGATG[C/G]AGTGTTGCTCTGTTG	8850
rs371801825	in-del	-/T			intron-variant	KAT2B	GRCh38.p7	3:20128505	GTTTTGTTTTTTTTT[-/T]GTTGCTAATTTATCT	8850
rs371804461	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20147904	TGATAAGTATTAACT[A/G]TGTTATTCTCTTGAC	8850
rs371812623	in-del	-/G			intron-variant	KAT2B	GRCh38.p7	3:20062259	TAATATATAAAATAT[-/G]ATATATAATATATAA	8850
rs371856560	snp	A/C	0.00755907	0.0610114	intron-variant	KAT2B	GRCh38.p7	3:20076537	TCCGTGCTTTTTGAA[A/C]AACTTTTTTTCTTAA	8850
rs371905290	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20061980	ATATATATTATATAT[A/G]AAACATATAATATAT	8850
rs371928511	snp	A/G	0.0123036	0.0774623	intron-variant	KAT2B	GRCh38.p7	3:20044849	ATTCTTAGCCATGCG[A/G]TTATTGACTAAGCGA	8850
rs371943920	snp	A/G	0.000153988	0.00877328	intron-variant	KAT2B	GRCh38.p7	3:20148004	AAAGAGAAAAGGTAA[A/G]TATGACGGGCAAGAG	8850
rs371989160	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20089026	GCATCTTTGTTGAAA[A/G]TCAGTTGACTGTAAA	8850
rs371998239	snp	A/C	1.65343e-05	0.00287521	intron-variant	KAT2B	GRCh38.p7	3:20127578	CAAGGTCTTAGAAGA[A/C]GAGCAGAATGTGGGG	8850
rs372005932	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20062265	ATAAAATATGATATA[A/T]AATATATAATATATA	8850
rs372018051	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038696	CCTTTAAGACTCTCA[C/T]CCTGCTTTGCGGAGA	8850
rs372035791	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20118987	CTGTTTTTGCCTCTT[G/T]TCTCAATAATGTGGT	8850
rs372053800	snp	C/T	0.000153988	0.00877328	intron-variant	KAT2B	GRCh38.p7	3:20114998	AAACAGGTAAGTTTC[C/T]TTTTACATGAATCAG	8850
rs372127593	snp	A/C	1.66799e-05	0.00288785	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20099926	CTTTGGAAAAGAAAC[A/C]CCCATTTGAAAAACC	8850
rs372129170	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20084131	TCTGAGAAGTTGGCA[C/T]ATTTAGACAACTACG	8850
rs372137807	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20071859	GTCTCATCTTCCTAA[G/T]ATTGCTAACTTCTTC	8850
rs372191144	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20053016	AGGTGCAGGGAGGTT[C/T]AGTAGCTAGCTTTGT	8850
rs372216063	snp	A/C	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20128930	GAAAATTGCTTGAAC[A/C]CGGGAGGCGGAGGTT	8850
rs372218405	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20050727	TTTTTTTTTTGAGAC[A/G]GAGTCTCGCTCTGTC	8850
rs372232659	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20104973	TCACTGCAACCTCCA[C/T]CTCCTGAGTTCAGGC	8850
rs372242549	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20127979	CGTGCTGTGCAGCCC[A/G]GTCCCTAACAGGCCA	8850
rs372249982	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20144428	CGAGTAGCTGGGACT[A/G]CAGGCACCCGCCACC	8850
rs372252029	snp	A/G			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038740	GCGAAACATCTCAGC[A/G]GAGCCAGGAGAGAGT	8850
rs372257036	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20126481	CTGTGGGCAATTATT[A/G]GGATATAAGACAGGT	8850
rs372260888	in-del	-/CTT			intron-variant	KAT2B	GRCh38.p7	3:20080080	GCAGCTTCTGGAGTT[-/CTT]ATTTCCATTCCTGCA	8850
rs372326302	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20062134	AACATATATATATAA[A/T]ATATATAATATATAA	8850
rs372340198	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20098158	TTGCTTGAGTCCGGG[A/T]TGCAGAGGTTGCCAT	8850
rs372368754	in-del	-/ATATA			intron-variant	KAT2B	GRCh38.p7	3:20062099	TATTATATATAAAAC[-/ATATA]ATATATATTATATAA	8850
rs372430785	snp	C/T	6.27018e-05	0.00559884	intron-variant	KAT2B	GRCh38.p7	3:20095459	TTATTCAAATGTACC[C/T]AGTCTCCATATGCCA	8850
rs372432629	in-del	-/TG	0.138694	0.224312	intron-variant	KAT2B	GRCh38.p7	3:20142885	GGGTATCTATGTGCC[-/TG]TGTGTGTGTGTGTGT	8850
rs372440670	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20088447	TTGATAATAGCTATC[C/G]TGAGCGTGAAGTGAT	8850
rs372460930	snp	A/G	1.65154e-05	0.00287358	intron-variant	KAT2B	GRCh38.p7	3:20072489	CTTCAAGGAAAGTAT[A/G]ACGAGTTCATTGTAG	8850
rs372590812	in-del	-/TTT			intron-variant	KAT2B	GRCh38.p7	3:20062200	TATAAAATATATATA[-/TTT]TATATAAAATATATT	8850
rs372624950	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20123183	CTCTCTGCGCCTCCC[C/T]ATATGCTCTTTTTCT	8850
rs372639814	snp	C/G	1.65971e-05	0.00288067	intron-variant	KAT2B	GRCh38.p7	3:20148222	TAATCATTGCTCCTT[C/G]TTTCCCTTTTTCCTT	8850
rs372680812	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20092385	AAGCATGTGCCGCCA[C/T]ATCCAGCTTATTTTT	8850
rs372698909	snp	A/G	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20075875	CGAGATCTCACCACT[A/G]CAGCCTGGGCGACAG	8850
rs372710550	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20119928	TTATTGTCATAGCTC[A/G]CTCATTTGGTGTGTT	8850
rs372719303	in-del	-/AA			intron-variant	KAT2B	GRCh38.p7	3:20084608	ATAAATGCAAAAAAA[-/AA]TCACAAAACCACAAG	8850
rs372751169	snp	C/T	5.00354e-05	0.00500152	synonymous-codon, intron-variant, nc-transcript-variant	KAT2B	GRCh38.p7	3:20148414	CAAGAGCCATCAAAG[C/T]GCTTGGCCCTTCATG	8850
rs372834383	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20138963	CTGTGGCATGATCAT[A/G]GCTCACTGCAGCCTC	8850
rs372874698	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038431	TCTCTGTTCATCCAC[C/T]CTTTACCCATGCATG	8850
rs372931610	snp	A/T	0.00517822	0.0506191	intron-variant	KAT2B	GRCh38.p7	3:20100203	GGGAAGAAAAACATT[A/T]AGTAGAACATGTAGT	8850
rs372942971	snp	C/T	4.94931e-05	0.00497434	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20101451	TGATATTTCTGGATA[C/T]AAAGAGAACTACACA	8850
rs372947222	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20142884	TTGGGTATCTATGTG[C/T]CTGTGTGTGTGTGTG	8850
rs372968016	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20130805	GTAGTTTTAGAAAAT[A/G]AAGATAATGAAGATT	8850
rs372985581	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20129245	TAAAAAAGCAAGTGG[A/T]ATCCAGTGAGATTAA	8850
rs373045477	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20081661	AATTAGTGTATATCA[A/G]TGCTTTGTATCAGGC	8850
rs373119307	snp	A/G	1.65201e-05	0.00287398	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20146372	AAAAGTTTACCCTGG[A/G]CTTTCATGTTTTAAA	8850
rs373175501	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20075740	GCCCTCTCCAGGTGC[A/G]CGACCCCCCAGGCAC	8850
rs373192795	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20134879	TAATTTTGACTTTTT[G/T]TTACTTAATATGTCT	8850
rs373230455	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20117396	ATGTCTGCGTATCGA[C/T]GCAACTGTGATAAAT	8850
rs373244060	in-del	-/AA			intron-variant	KAT2B	GRCh38.p7	3:20061833	AAGTATATAATATAT[-/AA]TATACATAAAATATA	8850
rs373253108	snp	A/G	7.25124e-05	0.00602087	intron-variant	KAT2B	GRCh38.p7	3:20122622	TGTATTATTTGTTTT[A/G]TGTTTAGAACCACCC	8850
rs373257280	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20123691	TGCATTTAATTCTTA[A/T]CTCTTCATTTGTTTA	8850
rs373264620	in-del	-/CA			intron-variant	KAT2B	GRCh38.p7	3:20140143	TCTTGATTCCTCACA[-/CA]GTGCCTGGAACATAG	8850
rs373348853	snp	A/G			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039703	TAGCAACAAAGAAAA[A/G]GATTAGCATGGACGG	8850
rs373400803	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20058566	AATCCCAGGCAGTTT[C/T]GTTCTCCTGAGGGAA	8850
rs373419053	in-del	-/TATAT	0.145978	0.227331	intron-variant	KAT2B	GRCh38.p7	3:20062374	ATATATAATTTATAA[-/TATAT]TATATATAACATAAT	8850
rs373419768	snp	A/G	1.89554e-05	0.00307853	intron-variant	KAT2B	GRCh38.p7	3:20099825	AGACATACCAATTAA[A/G]TTTTTCTTTTTCTTT	8850
rs373421620	in-del	-/T			intron-variant	KAT2B	GRCh38.p7	3:20062421	ATATATTATATATTA[-/T]TATATATAATATATA	8850
rs373454057	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20056890	TTACTTGTCCTACAG[A/G]GTTGTTGGGAGGGGA	8850
rs373460442	in-del	-/TTTTTTTTTTT			intron-variant	KAT2B	GRCh38.p7	3:20131022	GGCCTTTTTTTTTTT[-/TTTTTTTTTTT]GAGACGGAGTTTTGC	8850
rs373469804	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20127708	CTCCAATGGTCTCCA[A/G]CCTTTTTGGCACCAG	8850
rs373525362	snp	A/G	1.65247e-05	0.00287438	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20122755	CGATGGAATTAATCA[A/G]CGAGGTTATGTCTAC	8850
rs373527888	snp	C/T	1.65449e-05	0.00287614	intron-variant	KAT2B	GRCh38.p7	3:20148356	TTTGAAATGATTTCC[C/T]ACATGGAATTTCCAT	8850
rs373535725	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20123835	GTTTACTAAGGATTA[A/G]ATTCAAGTAAGGCAT	8850
rs373545712	snp	C/T	0.00478085	0.0486577	intron-variant	KAT2B	GRCh38.p7	3:20108044	TGAATTCTTGACCTC[C/T]GGTAATCCACCTGCC	8850
rs373605608	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20061114	CTTGCAAAACTGAAA[C/T]TCTGTGTTCATTAAA	8850
rs373650903	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20101072	TAGAATCACAACTCA[C/T]AGCCTCTCTGTCTTG	8850
rs373657180	snp	C/T	3.3211e-05	0.00407485	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152483	TATCCTGGAGAAATT[C/T]TTCTTCAGTAAAATT	8850
rs373659331	snp	A/G	1.74293e-05	0.00295201	intron-variant	KAT2B	GRCh38.p7	3:20101253	TAGTATGATTGCATA[A/G]CTGCATGAAGAAATT	8850
rs373699666	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20140865	GAGTCATTACTTTTT[A/G]AATTTGTGTAAAATA	8850
rs373721059	snp	A/C/G	0.000330226	0.0128461	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20125922	CAATTTTCTGTCAGC[A/C/G]CACTCGGCCAGGGAT	8850
rs373738745	snp	C/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20128973	GATCACAGCACTGCA[C/T]TCCAGCCTGGGCAAT	8850
rs373833642	snp	A/C	1.64901e-05	0.00287137	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20140289	GGATTATGAAGGAGC[A/C]ACTTTAATGGGATGT	8850
rs373836506	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20067895	GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG	8850
rs373875536	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20044025	AAAAAAGAAGGGAGC[A/T]AAGTCAGCCAGGGTG	8850
rs373908956	snp	G/T	5.18704e-05	0.0050924	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20137069	TTGGTTTCTCACCAC[G/T]CAACACTGTTTTGTC	8850
rs373924450	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20139015	CCTCCTGCCTCAGCT[A/G]CCTGTGTAATTGTGA	8850
rs373941573	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20140127	ACTTCAAAGAAGCTT[G/T]TCTTGATTCCTCACA	8850
rs373975643	in-del	-/AT			intron-variant	KAT2B	GRCh38.p7	3:20062025	TATTATATATAAAAC[-/AT]ATAATATATATTATA	8850
rs374022204	snp	A/C			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20040026	GGGGTGCAAACCCCG[A/C]GGGCAGCGGAAAAGA	8850
rs374059142	snp	C/T	0.00478085	0.0486577	intron-variant	KAT2B	GRCh38.p7	3:20094597	GAGAGAGTCAATGGA[C/T]AGGTCACAAAACTAT	8850
rs374072406	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20122150	TATCAGTAAGGCTCT[C/T]ACTGATATCCATACA	8850
rs374077988	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20106246	CAAATACCATCTTTA[C/T]TAGACATACAAAAAT	8850
rs374081547	snp	C/T	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20112621	TCTGTGATTATCATT[C/T]CGCCTAGATCAGCGC	8850
rs374082896	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20061919	TATATAAAATATGTA[A/T]TATATATCATATATA	8850
rs374098623	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20049816	CTGGCCCAATAGAAT[A/T]CTCTGTTGAAGAAAG	8850
rs374118051	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20092763	CTGGAGTGCACTGGT[A/G]TGATGTCGGCTCACT	8850
rs374195955	in-del	-/ATATAT			intron-variant	KAT2B	GRCh38.p7	3:20062182	TATATATAATATATA[-/ATATAT]AAAATATATATATTT	8850
rs374256390	snp	C/G			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039819	AGTGAAAGGACAAAT[C/G]ATTGAGAGGCTGCCC	8850
rs374263282	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20048738	AGTTTCCTACTCTTG[C/T]ATGCTGCTTTTCTGC	8850
rs374283840	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20093609	AGAGTAGACTGACCT[A/G]TGTCCAGCACCTGGC	8850
rs374298296	snp	G/T			intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20136731	ATTTTTATCTTTGAA[G/T]CAAGGATTTTGATTT	8850
rs374319232	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20102767	TTTTTTATAACTTTT[C/T]TATAACTTTTCTCTG	8850
rs374324427	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20124553	TCTGCCCTGATGATC[C/T]AACACTTCCCACTAG	8850
rs374329908	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20108485	ACATTTTAGTCAGCA[A/G]TGGACCACATATAAT	8850
rs374464691	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20131860	TGAGCCATTGTGCCC[A/G]ACCATAAACAGACGT	8850
rs374471209	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038905	GCCCTGTCTAAGCTA[A/G]TATCACTGTTTAGAT	8850
rs374488257	snp	A/T	0.00398564	0.0444627	intron-variant	KAT2B	GRCh38.p7	3:20041113	CTTTCCCGGGAGTGG[A/T]GCGGTGCTCTCCATG	8850
rs374529210	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20104958	GTGGCGCGACTCAGC[C/T]CACTGCAACCTCCAC	8850
rs374550574	in-del	-/GAAG			intron-variant	KAT2B	GRCh38.p7	3:20149548	TAAAAATGTGAAAAG[-/GAAG]AGTGAAAGGGACGCA	8850
rs374571237	in-del	-/TG			intron-variant	KAT2B	GRCh38.p7	3:20061915	ATTATATATAAAATA[-/TG]TATTATATATCATAT	8850
rs374706718	in-del	-/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20074863	TGTTTAACTCTGAAG[-/T]TTACCCCAAGGGAAC	8850
rs374775691	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20094445	GGAGACACAGAGCCA[A/C]ACCATATCAGAGCCT	8850
rs374789967	in-del	-/AC			intron-variant	KAT2B	GRCh38.p7	3:20073718	TTACCTTTTTAAAAA[-/AC]AATAAATAAATAAAA	8850
rs374802460	snp	C/G/T	0.00677024	0.0578401	intron-variant	KAT2B	GRCh38.p7	3:20124961	TGGTTGTGCTTCCAG[C/G/T]TATGGTTGAGTGTAG	8850
rs374814646	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20054642	GGTTTGTGTGGTATG[A/C]AGGAGGTTCCAGAAG	8850
rs374824398	snp	C/T	0.00636936	0.0560724	intron-variant	KAT2B	GRCh38.p7	3:20050936	CCGGGTATGGTGGCT[C/T]ATGCCTATAATCCCA	8850
rs374882370	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20128002	ACAGGCCACGGACTG[A/G]TAATGGTCTAGGGGT	8850
rs374883579	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20130210	GAGCTTTTTGTCTTC[A/G]ACTCCTAGCACTAAG	8850
rs374907679	snp	C/T	0.000583044	0.0170641	intron-variant	KAT2B	GRCh38.p7	3:20095444	AAACATTTTCTCTCA[C/T]TATTCAAATGTACCC	8850
rs374911835	in-del	-/C			intron-variant	KAT2B	GRCh38.p7	3:20124113	TCTTTCCATTTCCTT[-/C]CTAGATGTCCAGTCT	8850
rs374957962	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20062787	ATTATTAATGATGTT[G/T]AGCATCTTTTCATGT	8850
rs374963633	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20073385	TGCCATCATTTCTCT[A/C]GAGCTTCCTGCTTAC	8850
rs374984099	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20049220	TAGGAGTCCAGGTGC[C/T]ACCTCATTGACTTAT	8850
rs374993267	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20077170	GAACATTCAGTTGGG[A/G]ACTAGGAAGTAATAA	8850
rs374997182	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20089131	TTGATTGAGATAGCT[C/T]TGTAGTAGATTTTGA	8850
rs375008819	snp	G/T			intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20136593	AGCAGAAATTCATAA[G/T]CTACATTCATTCTGA	8850
rs375064127	snp	A/G	0.00358779	0.0422022	intron-variant	KAT2B	GRCh38.p7	3:20080841	CGTATTGAAAGAATA[A/G]TACTTTGGTATATAT	8850
rs375085710	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20145407	ACATATTCATGCTGC[A/G]GTATTTACCAGCTAT	8850
rs375101044	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20072721	AATAAGATGAAACAT[A/G]ACAATCGAGCTAGTT	8850
rs375104808	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20105466	GCTTACCCCCACACT[C/G]GGGAGATGTTTCATA	8850
rs375122069	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20091040	TATAGGCATGAGCCA[C/T]TGCACTTGGGCTTTT	8850
rs375143954	snp	A/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20113617	ATGACAACATTTAAG[A/G]CTATTGGGGATTTAT	8850
rs375147182	in-del	-/ACAG			intron-variant	KAT2B	GRCh38.p7	3:20075667	ATAAAGGATACACAG[-/ACAG]CCAGATGAAGGGATG	8850
rs375169189	snp	C/T	1.65351e-05	0.00287528	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20114925	TATAGTCAAAACTCT[C/T]CCATCTGGGATCAGG	8850
rs375170013	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20150396	ATATTCTGAAAAACT[A/G]TTTCTCTCATATGGA	8850
rs375207374	snp	A/G/T			intron-variant	KAT2B	GRCh38.p7	3:20095224	AATGTTTGGTTTCCA[A/G/T]TTGAGGTCTTACATA	8850
rs375277491	snp	A/T			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038896	TTGCCTTTTGCCCTG[A/T]CTAAGCTAATATCAC	8850
rs375283290	snp	A/G	1.79699e-05	0.00299744	intron-variant	KAT2B	GRCh38.p7	3:20099987	GCCCTCTTTTTATTG[A/G]CTCAAGGCTGAAGAA	8850
rs375299609	snp	C/T	4.95135e-05	0.00497537	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20119699	CCTGCCTGCAAAGCC[C/T]CTTCTGGACTTGAGG	8850
rs375345605	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20142558	CAGAATAAGTTGTAG[C/T]TGTCATTAGTAGAGA	8850
rs375377593	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20081081	GCCTTTTGCACATTA[C/G]TCAATTTGACAGATT	8850
rs375383719	snp	C/T	0.000116259	0.00762338	intron-variant	KAT2B	GRCh38.p7	3:20146434	TTCCTGGAATTAGTA[C/T]GTATAGACCTTCTTT	8850
rs375442309	in-del	-/CA			intron-variant	KAT2B	GRCh38.p7	3:20120160	GCAGGAAGAAATACA[-/CA]GTCTCTTGAAGCCTA	8850
rs375491076	snp	C/T	1.74668e-05	0.00295518	intron-variant	KAT2B	GRCh38.p7	3:20101246	TCAGAATTAGTATGA[C/T]TGCATAGCTGCATGA	8850
rs375575634	snp	G/T	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20095698	TTGCACATCTGTTCT[G/T]CATGTGGCACTAACG	8850
rs375588274	in-del	-/TAG			intron-variant	KAT2B	GRCh38.p7	3:20145552	CGGATGGGATTTTTT[-/TAG]TTTTTTTTTTTTTTT	8850
rs375649248	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20062544	TCGGCTCATTGTAAC[A/G]TCTGCCTCCTGGGTT	8850
rs375669279	snp	A/C			utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20153455	ATACACACAGCCACG[A/C]TGATAATATGCAAAT	8850
rs375772012	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20119936	ATAGCTCACTCATTT[A/G]GTGTGTTGCCTGAGA	8850
rs375775704	snp	C/T	0.00517822	0.0506191	intron-variant	KAT2B	GRCh38.p7	3:20138969	CATGATCATAGCTCA[C/T]TGCAGCCTCAACCTC	8850
rs375779524	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20088909	TCCATTTTGAATAGG[C/T]TTTTGTATATGGTAT	8850
rs375798522	snp	A/G	2.35513e-05	0.00343149	intron-variant	KAT2B	GRCh38.p7	3:20095433	TAACATTTTAAAAAC[A/G]TTTTCTCTCATTATT	8850
rs375806213	snp	A/G			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20069707	ATTTTTGTATTTTTA[A/G]TAGAGACGGGGTTTC	8850
rs375811086	snp	C/T			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039337	TCGATATTTATTCTT[C/T]TGAATTATGCTTATA	8850
rs375842216	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20061988	TATATATAAAACATA[A/T]AATATATAAAACATA	8850
rs375844921	in-del	-/AAG			intron-variant	KAT2B	GRCh38.p7	3:20048818	CACACATGGGGAGAG[-/AAG]GAGGGGAATCCTTGC	8850
rs375887576	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20079242	CAGAGTCTGGCTCTG[C/T]CACCCAGGCTGGAGT	8850
rs375898348	snp	C/T	0.000153988	0.00877328	synonymous-codon, intron-variant, nc-transcript-variant	KAT2B	GRCh38.p7	3:20127453	TGCTTTAATTAAAGA[C/T]GGCCGTGTTATTGGT	8850
rs375917512	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20067191	CTCAGTGGAGGAAGT[A/G]AAATCAGCCAGTTTT	8850
rs375947211	in-del	-/A	0	0	intron-variant	KAT2B	GRCh38.p7	3:20097530	AAAATAATGATTAAA[-/A]TTTTTTTTTAATTTT	8850
rs375961118	snp	C/T	0.000115423	0.00759593	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20148276	TGACCAGCTTTACAG[C/T]ACGCTCAAGAGCATC	8850
rs375993645	snp	C/T	1.65108e-05	0.00287317	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20111647	CAGTCTACCTCGGTA[C/T]GAAACCACACAGGTG	8850
rs376006797	in-del	-/GCA			intron-variant	KAT2B	GRCh38.p7	3:20086823	TTGAGATGGAGTCTC[-/GCA]GGCTGGAGTGCAGTG	8850
rs376017300	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20126133	GTGGTACTTTCTGTT[C/T]CTTCTTCCTTATTTC	8850
rs376023257	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20107134	ACCTCCTGGGTTCAA[A/G]CCATTCCCGTCTCTG	8850
rs376041573	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20100671	CCTCCAAACTCTATT[A/G]AATAAGAATTCATTG	8850
rs376085621	snp	A/G			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038051	AACACACTTTGAATA[A/G]GTCTTGAAACCACGG	8850
rs376108250	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20131280	TCGGCCTCCCAAAGT[A/G]CTGGGATTACAGTTG	8850
rs376169021	snp	C/G	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20082515	CATATCTGTTTAGTT[C/G]TCATGTCTCTTTAGT	8850
rs376186546	snp	G/T	6.64805e-05	0.00576505	intron-variant	KAT2B	GRCh38.p7	3:20148387	ATTAGATACCTTACT[G/T]TTTTCTTTACCCAAG	8850
rs376209161	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20142885	TGGGTATCTATGTGC[C/G]TGTGTGTGTGTGTGT	8850
rs376213765	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20124702	TAGTGTACTAGAGCT[A/G]GCTTGTACTGGAATG	8850
rs376243425	snp	C/G	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20076025	TAATCTTCTAATAAC[C/G]TGGTCTCTCTGGTGA	8850
rs376257618	snp	A/G	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20103773	ACTAAGAAATTGGTG[A/G]CACTTATGAATACTT	8850
rs376264367	in-del	-/CAA	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20072575	ACCTCTGTATGAGAG[-/CAA]CAACAAGAGCCTCTC	8850
rs376309145	snp	A/C/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20146810	CACATAGCCAGTAAC[A/C/G]GTCAGAATTAGAAGC	8850
rs376331395	snp	C/G	0.00597247	0.0543191	intron-variant	KAT2B	GRCh38.p7	3:20066301	GTCATTGGTTTTAGG[C/G]CTTAGGATAATTTCA	8850
rs376381067	snp	C/T	4.97475e-05	0.00498711	intron-variant	KAT2B	GRCh38.p7	3:20148371	CACATGGAATTTCCA[C/T]ATTAGATACCTTACT	8850
rs376391875	snp	C/G	0.000153988	0.00877328	intron-variant	KAT2B	GRCh38.p7	3:20119741	AAGCTCTTAAGAGGG[C/G]ATAAGAGAGGGCTGT	8850
rs376427623	in-del	-/A	0.198126	0.244559	intron-variant	KAT2B	GRCh38.p7	3:20044070	AGAGAATAGAAAAAG[-/A]AAAAAAAAAAAGAAA	8850
rs376469598	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20096694	TAAATTTTCCAGTGA[A/G]TTCCCTCTTTTGCTT	8850
rs376524638	in-del	-/TA/TATA	0.379571	0.215383	intron-variant	KAT2B	GRCh38.p7	3:20062464	ATATATATTTTATTT[-/TA/TATA]TATATATATATATAT	8850
rs376560592	in-del	-/TAA	0.00438332	0.0466095	intron-variant	KAT2B	GRCh38.p7	3:20082030	TCAATATACAGTTCC[-/TAA]TAATAAGGTTTTCTT	8850
rs376635109	snp	A/C	0.000163987	0.00905353	intron-variant	KAT2B	GRCh38.p7	3:20040784	TCCGCCTGCAAGGTA[A/C]GCGCTCGCCGCTCTC	8850
rs376649395	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20050005	AGGAGTTCGAGACCA[G/T]CCTGGGCAACACGGT	8850
rs376654765	snp	A/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20041126	GGAGCGGTGCTCTCC[A/T]TGTGGCGGGTGACCC	8850
rs376661670	snp	A/G	0.0107246	0.0724382	intron-variant	KAT2B	GRCh38.p7	3:20105166	GCTGGGATTAAAGGC[A/G]TGAGCCACCTTGCTC	8850
rs376664578	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20125205	GCAGGCTCCAGAGGC[G/T]GAGGCAGGAGAATGG	8850
rs376673410	in-del	-/TT			intron-variant	KAT2B	GRCh38.p7	3:20062411	ATTATATATTATATA[-/TT]ATATATTATTATATA	8850
rs376762888	in-del	-/G	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20072086	TAGCAAAGTGTGTGG[-/G]TCAGCTGCGTGAGCT	8850
rs376792522	in-del	-/CAAA			intron-variant	KAT2B	GRCh38.p7	3:20145650	ATTTTACAAAACAAA[-/CAAA]ACATCTCTCAAAATT	8850
rs376801435	in-del	-/AT			intron-variant	KAT2B	GRCh38.p7	3:20062259	AATATATAAAATATG[-/AT]ATATATAATATATAA	8850
rs376843877	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20061333	AAGGTTATATAATAG[C/G]CCTTTGAATGTATAT	8850
rs376888447	snp	C/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20047079	TTTTGTTTTGCCCCC[C/T]CCTTTTTTTTTTCTG	8850
rs376927131	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20093312	TAATTGGGAGCTGGT[A/G]TAGAACACTTACCTC	8850
rs376940329	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20062268	AAATATGATATATAA[A/T]ATATAATATATAAAA	8850
rs376968297	snp	C/T	0.000153988	0.00877328	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20140294	ATGAAGGAGCCACTT[C/T]AATGGGATGTGAGCT	8850
rs376968682	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20041859	ACTTCTGAATTTTGA[C/T]ATAACTATAATTTAT	8850
rs376972277	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20068846	GTTGGGGCCATTTAG[C/T]CATTTTTCTTTCTCT	8850
rs376998670	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20062189	AATATATAATATATA[A/T]AATATATATATTTTA	8850
rs377010780	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20046189	ATATCAGAGTCAGTG[A/G]CCACAAAGCATTTAT	8850
rs377019455	in-del	-/AC/ACAC			intron-variant	KAT2B	GRCh38.p7	3:20106438	AACAACACCAGAAGT[-/AC/ACAC]ACACACACACACACA	8850
rs377037575	snp	C/T	0.000277181	0.0117692	intron-variant	KAT2B	GRCh38.p7	3:20147956	GTTTCACTTTGTTGA[C/T]GTATAGGAGAGACAG	8850
rs377042076	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	KAT2B, MIR3135A	GRCh38.p7	3:20137742	ACCCAGGCTGGTCTC[A/G]AGCTCCTGGACTCAA	8850
rs377046987	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20141343	GACAGAGTTGAATAC[A/G]TAATAATTTCAAATT	8850
rs377063846	snp	A/T			intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20135661	TCCATCTCAAAAAAA[A/T]AAAAATAAAAACCAA	8850
rs377065504	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20084495	TATTTACATTTTCCC[C/T]CATCTCCATCTCCCT	8850
rs377077580	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20130110	AGCCACCTGAGTAGC[C/T]GGGATTACAGGCGTG	8850
rs377084393	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20105461	TTAAAGCTTACCCCC[A/G]CACTGGGGAGATGTT	8850
rs377087144	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20126777	TGGTGAGCCGAGACC[A/G]TGCCATTGCACTCCA	8850
rs377096260	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20132276	CTACTCAGAGGCTGA[A/G]GCAGGAGAATCACTT	8850
rs377109684	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20108773	TGAGCATTACAGCCT[A/G]AGCTCCACCTCCTGT	8850
rs377152704	in-del	-/TTTT	0.0333695	0.124785	intron-variant	KAT2B	GRCh38.p7	3:20141280	TGGTATTGAGGTGAC[-/TTTT]TTTATGCATATGAAT	8850
rs377212140	snp	C/T	0.000437904	0.0147905	intron-variant	KAT2B	GRCh38.p7	3:20147905	GATAAGTATTAACTA[C/T]GTTATTCTCTTGACC	8850
rs377245488	in-del	-/A			intron-variant	KAT2B	GRCh38.p7	3:20062251	AAATATATAATATAT[-/A]AAAATATGATATATA	8850
rs377268559	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070737	TATGCTGCTGGTCAC[A/G]GTGGCGCACGCCTGT	8850
rs377271448	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20064495	TTGGGTGAGAAGTTA[C/T]GGTTTTGATCCTTGA	8850
rs377320887	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20140825	ATCCTTGATCTGTTT[C/T]CTTTCTCGGTTACCA	8850
rs377342350	snp	A/G	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20062659	TAGAGACGGGGTTTC[A/G]CCTTGTTTGCCAGAC	8850
rs377361718	snp	A/G	0.00874735	0.0655527	intron-variant	KAT2B	GRCh38.p7	3:20139197	TGAGATTATAGGCAT[A/G]AGCCACTGCACCCAG	8850
rs377388027	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20112822	ATTCAGATAGTGTTA[C/T]TAGATTATGGAATTT	8850
rs377405463	in-del	-/TTCTTTTTTTTTT			intron-variant	KAT2B	GRCh38.p7	3:20144274	AGATTGCCCTTGGGA[-/TTCTTTTTTTTTT]TTTTTTTTTTTTTTT	8850
rs377405950	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20046399	CCAGCCTGGGCAACA[C/T]GGTGAAACCCTGTCT	8850
rs377460406	snp	A/G	0.0115144	0.0749975	intron-variant	KAT2B	GRCh38.p7	3:20060507	TGGGGAGGCTGAGGC[A/G]GGAGAATCTCTTAAA	8850
rs377468281	in-del	-/TATAT	0.490175	0.0693959	intron-variant	KAT2B	GRCh38.p7	3:20061834	GTATATAATATATAA[-/TATAT]TATACATAAAATATA	8850
rs377473233	snp	A/G	0.0158469	0.0875917	intron-variant	KAT2B	GRCh38.p7	3:20079473	CCTCCCCAAATGCTG[A/G]GATTACAGGCGTGAG	8850
rs377475879	snp	G/T	4.96093e-05	0.00498018	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20122738	AGTTATGGGGGATAT[G/T]CCGATGGAATTAATC	8850
rs377496534	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20116593	TTGAGAATGACTGTG[G/T]TAGACAATTCTCACC	8850
rs377522840	snp	C/G/T	0.00478085	0.0486577	intron-variant	KAT2B	GRCh38.p7	3:20065883	TTATAGTCTAGTGCA[C/G/T]CAATATCCAATAGTA	8850
rs377606078	in-del	-/T			intron-variant	KAT2B	GRCh38.p7	3:20116092	GTCCTTTTTTTTTTT[-/T]CTAACCTGAGATCGT	8850
rs377679644	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20053479	GGTCGAGGCTGTGGT[A/G]AGCCGTGAGTGTGCT	8850
rs377680654	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20040988	TTGAAGAAGGGGGAT[C/T]ACTAAGACGGAGAGC	8850
rs377690884	in-del	-/T	0.00517822	0.0506191	intron-variant	KAT2B	GRCh38.p7	3:20124736	AAGAAAATTGTTAAA[-/T]TTTCAGGAGTTTTGT	8850
rs377707301	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20041298	GGAGGAAAGCGCGGG[A/G]TGGGAAGGTGGGCAG	8850
rs377756015	in-del	-/GT	0.0023933	0.0345097	intron-variant, utr-variant-5-prime	KAT2B	GRCh38.p7	3:20071528	CTGCTGAAGCATACA[-/GT]GTGGTACCTGGTAGA	8850
rs386396081	in-del	-/AGA			intron-variant	KAT2B	GRCh38.p7	3:20113950	GGAAAAAATGAAGAA[-/AGA]GACCACTGATAGCTT	8850
rs386659078	multinucleotide-polymorphism	CT/GC			intron-variant	KAT2B	GRCh38.p7	3:20068375	TGTTGAGCAAGCCAG[CT/GC]ACTCTCTTGCCTTTG	8850
rs386659079	multinucleotide-polymorphism	CA/TG			intron-variant	KAT2B	GRCh38.p7	3:20068530	TAAGTTCCCTGTACT[CA/TG]TCCTTTTTTCTTTCT	8850
rs386659080	multinucleotide-polymorphism	CA/TG			intron-variant	KAT2B	GRCh38.p7	3:20090614	TCTGTTGTGTATTTT[CA/TG]CATCCATGTTCATCA	8850
rs386659081	multinucleotide-polymorphism	ACG/GCT			intron-variant	KAT2B	GRCh38.p7	3:20090695	TGGTATTAGTATAAT[ACG/GCT]GACCTTGTAAAGTGA	8850
rs386659082	multinucleotide-polymorphism	AG/CT			intron-variant	KAT2B	GRCh38.p7	3:20098966	TTGTTTCTACTGAAA[AG/CT]GCAGTAAGCGAGAAA	8850
rs386659084	multinucleotide-polymorphism	CTA/TTT			intron-variant	KAT2B	GRCh38.p7	3:20106593	AGTATAAATTGAGGT[CTA/TTT]TAAAATGACTTTGAG	8850
rs386659085	multinucleotide-polymorphism	ATA/CTG			intron-variant	KAT2B	GRCh38.p7	3:20130545	TTTTTATTTTCAAAG[ATA/CTG]GCTATACCAAACACC	8850
rs386659086	in-del	AT/TTAA			intron-variant	KAT2B	GRCh38.p7	3:20146671	AATATCCACCACTTA[AT/TTAA]GAGTCTGCCATTTGT	8850
rs397707625	in-del	-/G			intron-variant	KAT2B	GRCh38.p7	3:20150890	CCCCTTTTTGGGGGG[-/G]TACATGTTTCTTCCT	8850
rs397708539	in-del	-/A			intron-variant	KAT2B	GRCh38.p7	3:20074102	GAATGAAAAAAAAAA[-/A]TCACATATCCTTTGA	8850
rs397716148	in-del	-/T	0	0	intron-variant	KAT2B	GRCh38.p7	3:20147097	CCATTGAATATCATT[-/T]GGCAATTTTGTTCAG	8850
rs397749721	in-del	-/CTA/CTT	0	0	intron-variant	KAT2B	GRCh38.p7	3:20139223	CCAGCCAGACTTCTT[-/CTA/CTT]TTTTTTTAAAAATGT	8850
rs397762383	in-del	-/T	0.375	0.216506	intron-variant	KAT2B	GRCh38.p7	3:20089367	AAGTGATAAGATATC[-/T]TTTATGTTCACAGAT	8850
rs397776864	in-del	-/AA			intron-variant	KAT2B	GRCh38.p7	3:20051214	AAAAAAAAAAAAAAA[-/AA]CCCAAACAAAAAAAA	8850
rs397802993	in-del	-/A			intron-variant	KAT2B	GRCh38.p7	3:20110691	AAAAAAAAAAAAAAA[-/A]GAAAGAAAAAGAAAG	8850
rs397841560	in-del	-/T			intron-variant	KAT2B	GRCh38.p7	3:20139807	ATCACTTTATTTTTT[-/T]GACCATCTTTTCTTT	8850
rs397877197	in-del	-/A			intron-variant	KAT2B	GRCh38.p7	3:20043730	GATTTGCTTTTTTTA[-/A]AAAAAAAAAAAATTT	8850
rs397877959	in-del	-/C			intron-variant	KAT2B	GRCh38.p7	3:20060945	GACCCTGTCTCAAAA[-/C]AACAACAACAACAAC	8850
rs397964949	in-del	-/A			intron-variant	KAT2B	GRCh38.p7	3:20098248	TAAAAAAAAAAAAAA[-/A]GTCAGTCTTAGATGT	8850
rs398051658	in-del	-/T	0.5	0	intron-variant	KAT2B	GRCh38.p7	3:20047625	TTTTTTTTTTTTTTT[-/T]GAGACGGAGCCTCAC	8850
rs398051659	in-del	-/T	0.5	0	intron-variant	KAT2B	GRCh38.p7	3:20104904	TGTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCAC	8850
rs398062135	in-del	-/AA			intron-variant	KAT2B	GRCh38.p7	3:20043741	TTTAAAAAAAAAAAA[-/AA]TTTAACTGGACTTGA	8850
rs398062136	in-del	-/CT/T	0.425277	0.178263	intron-variant	KAT2B	GRCh38.p7	3:20112166	AAAGAGCTCAAGTGG[-/CT/T]TTTTTTTTTTTTTCC	8850
rs398062137	in-del	-/TT			intron-variant	KAT2B	GRCh38.p7	3:20148046	AAGTGATTTTTTTTT[-/TT]CCCCACCAAGCAACT	8850
rs398081940	in-del	-/A			intron-variant	KAT2B	GRCh38.p7	3:20097529	AAAAATAATGATTAA[-/A]ATTTTTTTTTAATTT	8850
rs398081941	in-del	-/T			intron-variant	KAT2B	GRCh38.p7	3:20114535	AAATATTAGTAACTT[-/T]TATGATGGTAATGAC	8850
rs398091335	in-del	-/T			intron-variant	KAT2B	GRCh38.p7	3:20068269	CCAAAGTGCTGCAAT[-/T]ATAGGTGTGAGCCAC	8850
rs398091336	in-del	-/A			intron-variant	KAT2B	GRCh38.p7	3:20141379	AGGCAGAAAAAAAAA[-/A]CACTCATGATGAAAA	8850
rs527247551	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20092597	TACAGCAAACATTAG[A/G]TGCTGTAACATTAGG	8850
rs527270655	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20143368	ATGGCTATTATTAAG[A/C]AGTTAAAAAAATAAC	8850
rs527296146	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20142787	AAACAGATTTGTGGG[C/T]ACATGAACAGGTAGG	8850
rs527302416	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20054894	GGTTAGGGGCCTGTG[A/G]CCACTTCTCTGCTAC	8850
rs527313164	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20089762	ATCTCCTTGGCTAAA[C/T]TTATTCCTAGGTATT	8850
rs527385829	snp	A/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20085803	GGCATGAGCCACTGC[A/G]CCCTGCCTACATGTA	8850
rs527398102	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20093041	CTGATATAAACATAG[C/T]TGCTCCTGCTCCTTC	8850
rs527414619	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20042853	GGGATTTGAGTGTTT[C/G]CTGGTCACTTTCATG	8850
rs527453194	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20076543	CTTTTTGAAAAACTT[C/T]TTTTCTTAATGGAAA	8850
rs527454810	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20105571	CGCTTGAGCCCAGGA[G/T]TTTGAGCCCAGCCTG	8850
rs527527609	snp	A/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20066045	TTTGGAGGCTAGAAG[A/T]CTGAGATCAAGATGT	8850
rs527542613	in-del	-/T	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20121201	TGATTTAGTAAATAA[-/T]ATGTAATACTTCTGG	8850
rs527546331	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20112657	CAGGAAGGTAAAAGG[C/T]GTAATTTGAAAAGGC	8850
rs527551396	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20054416	GATTACAGATGTGAA[G/T]GAGATGGATGCATTT	8850
rs527556301	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20086102	ATGGTGAAACCCCAT[C/G]TCTACATAAAAATAC	8850
rs527562935	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20099172	CTTTAAATTCCAGTG[A/G]CAGGAATTAAGAGCA	8850
rs527593543	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20098438	CTACCTCAAAAGGTT[G/T]TAAGTATTAAATGAG	8850
rs527645715	snp	C/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20041942	GTCACAATGGAATGT[C/G]TATGCTTGCTCTTTT	8850
rs527680841	snp	A/C	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20134352	TTCGTCTTCTCTTTA[A/C]CACCTTGATTATGGT	8850
rs527715517	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20077972	TTGAGCCCAGGAATT[C/T]GAGACCATCTTGGGC	8850
rs527738376	snp	A/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20106774	TGTATCAGAAATAAT[A/G]TCAGTCTTAGAGCCT	8850
rs527745485	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20072078	GGGGCAATGGTAGCA[A/G]AGTGTGTGGGTCAGC	8850
rs527807420	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	KAT2B	GRCh38.p7	3:20071403	TAAATGGTGAGAGTG[A/G]CAGAGTGCTAAGAAT	8850
rs527828718	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20098164	GAGTCCGGGATGCAG[A/C]GGTTGCCATGAGCTG	8850
rs527833109	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20075423	TCCCATAATTCATTT[C/T]GGTTCTGACATGACC	8850
rs527847537	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20097464	TTGGGCAAATAAGTT[A/G]TAAATAATCTATTCC	8850
rs527862313	snp	A/C	0.00676609	0.0577691	intron-variant	KAT2B	GRCh38.p7	3:20141221	TGCTTTTACTTGGCA[A/C]GTTCTGAAGGCTTAT	8850
rs527874752	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20047359	TTACAGGCATGAACC[A/G]CCACGCCTAGCCTAA	8850
rs527883816	snp	A/G	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20053772	AATTGTTCCTTTACC[A/G]TTTAGGCTTATTTTT	8850
rs527895171	snp	C/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20140733	CTGACCTCAAGTGAT[C/G]CACCTGCCTCGGCCT	8850
rs527895979	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20053095	ATAGTTAAGTGTGTT[G/T]CCCCTTGGTTCATGG	8850
rs527994310	snp	A/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20090927	ATTTATTTATTTTTA[A/T]TTTTTGTAGAAACAG	8850
rs528022648	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20048067	GGTGGATAAGATGTT[A/G]TTTTAAAAGATCAGT	8850
rs528041810	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20110949	AAATGGTAGAAGCTT[A/T]ATACTTCCTACATTT	8850
rs528076163	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20064338	CAATCACTTGTCATT[C/T]CTTTGTGATGAGAAC	8850
rs528082488	snp	C/G	0.000399281	0.0141238	downstream-variant-500B	KAT2B	GRCh38.p7	3:20154561	AGGTCATCAGTAAGA[C/G]ATTTTCAGGAGAGAC	8850
rs528090064	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20110406	CTCAGTTTGGTAGCT[C/T]ATGCCTGTAATCACA	8850
rs528102606	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20118029	CTGGTTATAAACCAA[C/T]TGTTAACATTTTGCC	8850
rs528150823	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20104617	CCTCAGGACCTATAA[C/T]GCTGGTTCAGCTTAT	8850
rs528154083	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20096652	TTTATATTTATTTGT[A/G]CTTCATTTTTATATG	8850
rs528167476	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20058934	ATCTCAGGTTCCACC[C/T]GACACCCACTGAATC	8850
rs528204160	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20068000	TTTTTCTTTCTTTCT[G/T]TTTTTTTTGTTTTTG	8850
rs528221682	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20124797	AAGTTGACTAGCATG[A/G]CACCTGGTTACCTGG	8850
rs528244267	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20151056	ACATTTTGATCTGTT[C/T]AGTCACACTTGGATG	8850
rs528251064	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039202	ACGGTACACCACTTT[C/T]AAACGCAGCACTGAC	8850
rs528284350	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20124611	TTTCAGCATGAGATT[C/T]GGAGGGGTCACACAT	8850
rs528294887	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20132102	AATTTGGGCCAGGCG[G/T]GGTGGCTCACACCTG	8850
rs528297831	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20082552	TAATCTGGAGTTCCT[C/T]AGCATTTTATTTTAT	8850
rs528301381	in-del	-/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20144040	CAATAAATTAAAAAA[-/G]ATCTCTTCTCCATAC	8850
rs528310361	snp	A/G	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20046357	GTGGCCAAGGCAGAC[A/G]GATCACTTGAGCTCA	8850
rs528370030	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20152003	TGTATAATTCTGACT[C/G]AATAGCTAACAGTAG	8850
rs528374542	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20127870	CACGCATAGTTCACA[A/G]TGGGGTTTGCACTCC	8850
rs528391892	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20076032	CTAATAACCTGGTCT[C/G]TCTGGTGAGCAGCTT	8850
rs528402933	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20117566	GCCTGGCACTTTAGT[A/G]TATTCTGATTTTTGA	8850
rs528436960	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20129952	GCTTCACTCTCTGGT[A/C]ACAGTACCCATTTTT	8850
rs528464245	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20146838	AGCAGCCCAGTTCTG[A/G]TGGCCGAACACCTTA	8850
rs528469246	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20138997	CTCCTGGGCTCAGGC[A/G]ATCCTCCTGCCTCAG	8850
rs528490029	snp	A/G	4.95585e-05	0.00497763	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20146358	CAGGCACAAATTCGA[A/G]AAGTTTACCCTGGAC	8850
rs528518910	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20042437	AGAATTAAGAACAAG[C/G]TCATGGGTACAGGGC	8850
rs528536467	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20066838	ATATTATTATAATAT[A/G]TAATCAATATAAAAT	8850
rs528579199	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20089461	ACTGGAGTGCAATGG[C/T]GCAATCTCAGCTCAC	8850
rs528580962	snp	G/T	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20088531	TCCATATACCTGTTG[G/T]CCATTTGTATGTCTT	8850
rs528591635	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20095959	GTTGAGCAGAAACCT[A/G]AGTGGGAGATAGGAG	8850
rs528611430	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20091907	TGCACCAATCCAATA[C/T]TTTCCTACCAGTGTG	8850
rs528618226	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20123665	TGAAGGATCAGTTAG[G/T]GATTGTGCATTGCAT	8850
rs528624729	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20139843	TTTAGATCAATGTTA[A/G]TTATTGATTTGCTGA	8850
rs528637428	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20116766	CCTTTTCACAAACCC[A/T]GGGAAGTTGGAATTA	8850
rs528639698	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20100221	TAGAACATGTAGTTT[G/T]TAAGAAGAACACATG	8850
rs528656989	snp	A/G	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20089790	ATTTGATTGTTTTTG[A/G]TGCTGTTATAAATGA	8850
rs528675066	snp	C/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20152090	GATTGAACCAGATGA[C/T]TAATAATGGTCCCTT	8850
rs528692079	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20116064	TACCAAAAACATGTC[A/G]AAAACATCTTTGTGT	8850
rs528713289	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152746	TAGATTTTAATCTAT[G/T]TACTACTATTAAGGT	8850
rs528733609	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20056924	TAACATGATTTGGAC[G/T]GCAATTGCCTTGGAA	8850
rs528811099	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20081817	AACGAAGAATATCCC[A/G]TAAATCCTTTCCCTA	8850
rs528850644	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20104719	ATGAAGTTAAACAGG[A/G]TTCTTTGTGGAAAAG	8850
rs528862446	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20065184	AGTGGCCTTTTCTTC[C/T]TTCTTGGTTCTGCAA	8850
rs528875184	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20074808	TGTGAGTATTGGTTC[A/G]GGATTTAAATACCCT	8850
rs528883027	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20054937	AAGCAAAAGCCACAA[A/G]GAGCCCTTTTCTTGT	8850
rs528886880	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20059051	TCAAACTGCTCATTT[C/T]CAAAGAGAAAACTTC	8850
rs528891564	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20148722	CTTAACGACACTAGA[C/T]GCAGAAAATCCACGG	8850
rs528954459	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20091092	TTAGTTCTTTTTAAA[A/G]TGTTTGGTAGAATTC	8850
rs528968524	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20097598	CTAGAGTGAAGTGGT[A/G]TGATCTCAGCTCACT	8850
rs529034340	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070603	CCCACCGTGCCCGGC[C/G]TCTCTTTTCTTATAC	8850
rs529058216	snp	G/T	0.0252325	0.109451	intron-variant	KAT2B	GRCh38.p7	3:20118330	TTTTCTCCTAAATTT[G/T]TGTGTGTGTGTGTGT	8850
rs529058312	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20126201	GTCAGCCATAGTCAT[A/C]CACCGAATACTACTG	8850
rs529104847	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20051167	ATCACACCACTGTAC[C/T]GTAGCCTGGGTGACA	8850
rs529120219	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20071303	ATGTAGATGGCTCTA[C/T]CCTAGAGTGACTTCA	8850
rs529142773	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20064473	ATATTTGGTTAGAGA[A/G]ATCTTATTGGGTGAG	8850
rs529217188	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20111113	AGGGTCTTCCTCAGC[C/T]TCTCCTTTAATTTTT	8850
rs529246487	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20046427	TCTCTACAAAAATTA[C/T]GAAAATTAGCCGGGC	8850
rs529248375	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20052950	CACTGCACTCCAGCC[A/T]GGGCGACAAGAGCTA	8850
rs529252731	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20132146	TTGGGAGGCTGAGGC[A/G]GGCGGATCACCTGAG	8850
rs529288814	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20139876	ATCCTGGGGACCCCC[C/T]CACCACTTTTGGAGA	8850
rs529304897	snp	A/G	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20089550	AGATTACAGGCGTGC[A/G]CCACCATGCCCGGCT	8850
rs529384151	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20047232	GGCCGGCTAATTTTT[G/T]TATTTTTTATAGAGA	8850
rs529389714	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20082711	CAAAACCTTAAAGAA[C/T]TGCCAACGTAGATAT	8850
rs529406041	snp	C/G/T	0.000399281	0.0141238	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039301	GGGTTTTTTTTTTCT[C/G/T]TTTAAAGTTTGAGGC	8850
rs529409540	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20138670	TTTCCATGTTTATCA[A/G]TTCTTTGTATTTGTT	8850
rs529438348	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20153728	ACCAACTAATATACA[A/C]CCATATAAATGAAGG	8850
rs529448274	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20049045	TTTTGTATTTTTAGT[A/G]GAGACGGGGTTTCAC	8850
rs529462632	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20110085	TTATTCCTCTCTTCA[A/T]TAAAGGGCTCAAAGT	8850
rs529473279	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20063882	TTTCATCTATTTTGA[G/T]TTCATTTGTGTGTGT	8850
rs529478909	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20102214	CTGGCTACTTGGGAG[G/T]CTGAGGCAGGAGAAT	8850
rs529498951	snp	C/T	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20146919	TGCTTGACTAGTCTC[C/T]CCAAACTTCTAAAAA	8850
rs529508801	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20063445	TTTCTTTCTTTCTTT[C/T]TTTTTCTTTTGAGAT	8850
rs529517502	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20051989	TCAAACTTCTTAAGA[C/T]AATTTATCACCTAGT	8850
rs529561540	snp	A/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20058348	TAATCTCAGCTACTC[A/G]GGAGGCTGAGGCAGG	8850
rs529649546	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20116169	TCTGTGCCTATTACA[C/T]GTTTCTTCTACAGTT	8850
rs529652687	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20117823	TCATCAGCTACCAGT[C/T]AGCAACACAGCTAGC	8850
rs529714814	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20131165	GGATTACAGGTGTCA[G/T]CCACCATGCCCGGCT	8850
rs529730952	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20124170	AGGGATTTAGTAACA[C/T]TACAGATTAGCTGAG	8850
rs529741208	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20109531	CTATGTTGCCCAGGC[C/T]GGTCTTGAACTCCTG	8850
rs529752749	snp	G/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20090967	ATGTTGTGCAGGCTT[G/T]TCTTGAACTCCTAGG	8850
rs529765633	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20102739	GTGACTTGGGTCATC[C/G]ATTCTTTTCAACTTT	8850
rs529769971	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20048591	AGATGCCTGGGAGCA[G/T]TCAGCACATCTGCTT	8850
rs529772406	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20069206	TAGAACTTGGGCTTA[C/T]AGGCTATCTCAGCAA	8850
rs529831889	in-del	-/A			intron-variant	KAT2B	GRCh38.p7	3:20117537	CCTATATATTGGGAG[-/A]AAAAAAACATAGAGC	8850
rs529836850	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20100801	GGTAAGCTTATTGAC[C/T]TCAAACAAATGATAG	8850
rs529837273	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20126380	TCTTTATAGCAGTGA[A/G]AGAATGTAACACTAA	8850
rs529840315	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038399	CTATTATATGGACCC[C/T]TATTTGCTTTATCAT	8850
rs529902973	snp	A/G	0	0	intron-variant	KAT2B	GRCh38.p7	3:20081315	AGGCCAATGATACAC[A/G]GAGCCAGAGGTTAGT	8850
rs529916287	snp	C/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20137203	CAAAAATAAGCTTCA[C/G]CCTGGATTAGAGAGT	8850
rs529920919	snp	C/T	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20056832	TTGTTCTTTGCCAGC[C/T]GAGTGAACTCAGGCA	8850
rs529926733	snp	C/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20050452	CTCCTCCCCACTCCT[C/G]GTAATCCTTATTCTG	8850
rs529964499	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20087538	AATTGATTCTGTTAG[A/C]AATTTTCAATTATAT	8850
rs529971647	snp	G/T	0.00398564	0.0444627	intron-variant	KAT2B	GRCh38.p7	3:20130627	AAAGGGAAACTGAAG[G/T]TATTTAATACGAATT	8850
rs529980957	snp	G/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20044963	ACTAAGTAGAGATTT[G/T]TCATATAGGACAGTT	8850
rs530015801	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20107911	CCTCCCAGGTTCAAA[C/T]GATTCTCCTGCCTCA	8850
rs530024150	snp	A/G	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20061719	TTTGTATTTTCATAC[A/G]TATATATGAAAAAAT	8850
rs530131097	snp	A/C	1.73228e-05	0.00294297	intron-variant	KAT2B	GRCh38.p7	3:20101258	TGATTGCATAGCTGC[A/C]TGAAGAAATTGCCTT	8850
rs530141661	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20100653	TCAGTAAATTTTATT[C/T]TGCCTCCAAACTCTA	8850
rs530172139	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20151866	TTTATTATCAGTTTC[C/T]CTATATGACACCAAA	8850
rs530276643	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20121811	AGCACAGAGATTCCA[A/G]TCAGTGGGTAGACTC	8850
rs530276982	in-del	-/A	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20092800	CCGCCTCCTGGGTTC[-/A]AAGCAATTCTCCTGC	8850
rs530278067	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20141145	GCACCAGTTTGATCC[A/G]CCTATTTGAATTTCA	8850
rs530287827	snp	A/G	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20073958	CTCCATTCTAAGCAC[A/G]TAAACACACATGAAT	8850
rs530341642	snp	C/G	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20128865	ATACAAAATTAGCTT[C/G]GTGTGGTGGCACATG	8850
rs530376041	snp	A/C	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20067440	CACAGCCATTATTCT[A/C]TGTCATGTTAAGACA	8850
rs530379592	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20117527	AATTCAGAAGGCCTA[C/T]ATATTGGGAGAAAAA	8850
rs530443836	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20116963	GGTGTGTGCTGCCAA[C/T]ATACAGCATACACTT	8850
rs530474193	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20114394	CCACTTACAACACTG[A/C]CTATCATGTAGTAAG	8850
rs530504316	snp	C/T	0.00557542	0.0525036	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20069986	CTCTGAAGAGGTGGA[C/T]GGTTCATTACAGAGA	8850
rs530535625	snp	A/C			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20069905	CATATTCTCCTATTC[A/C]CTGTCTTCATTGTAA	8850
rs530546683	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20124356	AGCTTCTGGGGAGGC[C/T]TCAGGGAACTTATAC	8850
rs530554132	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20132922	CGACATCCGTGTTAA[A/C]GTGAATTTCATTAGA	8850
rs530558688	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20069327	GGAAACCAATGGTAG[A/C]TCAGGGCTGGTTTTA	8850
rs530609772	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20131217	AATGGTGTTTCATCA[C/T]GTTGGCCAGGCTGGT	8850
rs530675357	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20045441	CTGCAGCCTTGAACT[C/T]CTTGACTCAGGTGAT	8850
rs530690139	in-del	-/T	0.132751	0.2208	intron-variant	KAT2B	GRCh38.p7	3:20144800	ATTTCTTTCTTTTTC[-/T]TTTTTTTTTTTTTAA	8850
rs530738453	snp	A/T	0.00358779	0.0422022	intron-variant	KAT2B	GRCh38.p7	3:20045001	TCCCACAGATATTGA[A/T]AGGATTGGGTTATTT	8850
rs530738792	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20081964	TTGTTTTTCTGGAAC[C/T]ATATGAGAATAAGTT	8850
rs530842210	snp	A/G	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20152005	TATAATTCTGACTGA[A/G]TAGCTAACAGTAGTC	8850
rs530884337	in-del	-/AGATAGATAGAT	0.0103295	0.0711199	intron-variant	KAT2B	GRCh38.p7	3:20109284	CTTCCCCTCAGCCCC[-/AGATAGATAGAT]AGATAGATAGATAGA	8850
rs530923856	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20145188	AATGACATTTTAGAT[A/G]TAATGGGTTAAATGA	8850
rs530928397	snp	A/G	5.24315e-05	0.00511986	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152568	CTCACCAAGCAGTGT[A/G]CCTAAAGCAAGGTGG	8850
rs530941104	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20045677	CATTTATATTAATAC[A/G]TAAGAGGAGGCAATA	8850
rs530963813	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20104571	GGCTGCAGGCACCAG[C/T]AGGCTTTATCTTGAT	8850
rs530985357	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20138246	TCCTCTCAGCTCATA[C/T]CTATGCTGTTAATGC	8850
rs530986543	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20068058	CTGGACTGCAGTGGC[A/G]CAATCTTGGCTCACT	8850
rs531036399	in-del	-/AG	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20123509	TTGAATAATTGAGAC[-/AG]GGAATGTGTGGCTTG	8850
rs531073974	snp	A/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20061798	ACATAAAATATATTA[A/T]ATATTATATATTATA	8850
rs531081326	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20115239	CCAGGTATAATGGTG[A/G]ATAGTGAGTGAAAGC	8850
rs531095948	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20108724	TGGCTCATTAGGAAC[C/T]GGGCTGCACAGCAGG	8850
rs531111517	snp	A/C	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20074568	GTAGTGGTACTATAA[A/C]ACTATCAGGGTTCTT	8850
rs531131388	in-del	-/TTTC	0.0015984	0.0282249	intron-variant	KAT2B	GRCh38.p7	3:20067990	TTCATTTCTTTTTTC[-/TTTC]TTTCTTTCTTTTTTT	8850
rs531135574	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20066465	GTGCAGTGGTGCCAT[C/T]TCAGCTTACTGCAAC	8850
rs531219148	in-del	-/TATAT	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20061791	TTATAATACATAAAA[-/TATAT]TATATATTATATATT	8850
rs531267465	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20080579	ATTGTGCTTATTCTT[C/T]TGTTGGTAAATAGTC	8850
rs531337720	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20129611	GAACTCCTGACCTCA[A/G]GTGATCTGCCCTCCC	8850
rs531344473	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20044043	GTCAGCCAGGGTGAC[A/G]TGCCACACCCCAGAG	8850
rs531363789	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20096390	GTGGGAAGGAAACTG[A/G]TGGTGGAAATGGATA	8850
rs531369790	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20086474	GGCATGGTGGTACAC[C/G]CCTATAGTCCCAGCC	8850
rs531370173	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20093624	GTGTCCAGCACCTGG[C/G]AGATATTCCTCAATA	8850
rs531399849	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20150758	ACACCGCCATAATTC[C/T]TGCTTTGTTTCTGCT	8850
rs531434797	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20150237	GTATTTTTTTTCTTG[G/T]TATTGTTCAGATGCT	8850
rs531457745	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20086959	GATAATTTTTATATT[C/T]TGAGTAGAGATGGGG	8850
rs531459021	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20143467	GCCCCTGTGGAAAGC[C/T]GTTTGGAGATTTCTC	8850
rs531459129	snp	A/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20079952	TTTGGTATAAGTTAT[A/G]TCTCCCTGACGTCCT	8850
rs531519995	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20099788	GAGACAGACAGAAAC[A/G]GAAGAGAGAGGAGAG	8850
rs531524976	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20054962	TCTTGTTGAGGAGAC[A/G]GATATTAAGTGAAAG	8850
rs531527040	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20076307	ATTTTCTCAGGGTAC[A/G]GGGGGTATAGGTATT	8850
rs531529833	snp	G/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20080521	CTGTGATTAAGAGTT[G/T]ACTTTTTCTCTAGTT	8850
rs531536745	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20055667	GTAGGAGATTAGGTG[G/T]AAGGGATAAATGGGG	8850
rs531539542	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20060532	CTTAAACCCAGGAGG[C/T]GGAGGTTGCAGTGAG	8850
rs531555904	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20120946	ATTCATGCAGAAACT[C/G]TTTACCAGTGAGCTT	8850
rs531597567	snp	C/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20052957	CTCCAGCCTGGGCGA[C/G]AAGAGCTAGACTCCG	8850
rs531616365	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20120286	TGGCTGGAGTGCAGT[A/G]GTGTGATCTCAGCTC	8850
rs531654232	snp	C/T	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20079147	CTCAGGTGATCCACC[C/T]GCCTCGGCCTCTCAA	8850
rs531675073	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20114226	GCATAGTAATTAATC[A/G]CTGGTTCCAATCCTG	8850
rs531699858	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20140615	CGTACCTCAGCCTCC[C/T]GAGTAGCTAAGATTA	8850
rs531736985	snp	G/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20113707	GGGCACTGTTTCAGA[G/T]TGAGAGCTGGGACCG	8850
rs531761310	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20042620	ATGCAGGAACTGTCT[C/T]AACTCAGTGTTTCTG	8850
rs531806244	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20066681	GCTGGGATTACAGGC[A/G]TGAGCCACCGCACCT	8850
rs531815810	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20106102	AACCACAGGATTTTC[A/G]GTTCAGCAAGTCAGT	8850
rs531821246	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20054303	GCAGCTAATTTTTGT[A/G]TCTTTAGTAGAGACG	8850
rs531829943	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20133911	ACTGGTAATATTTAT[C/T]CTTGTTCTAGCCTTT	8850
rs531925047	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20051172	ACCACTGTACTGTAG[C/T]CTGGGTGACAGAGCA	8850
rs531940017	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20048657	AGGATTTTCAAGGCT[C/T]AGTGGCTTCTGATTT	8850
rs531955372	snp	C/T	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20135285	GTTTACTAGACATAC[C/T]GTCCCCTTATTATTA	8850
rs531956627	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20048169	AAAGCCAAGCATACA[A/G]AGGAAAAAATGTTTC	8850
rs531990812	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20078497	TTCACTTCAGCCTCT[C/T]GAGTAGCTGGGACCA	8850
rs532027966	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20044251	TTTGGGAGGCCGAGG[C/T]GGGAGGATCACTTGA	8850
rs532062043	snp	G/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20127305	GGCTACATGAAGGAA[G/T]TTTCTATAGAAACTT	8850
rs532070197	snp	A/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20074676	CTAGAAGCTGAAAAC[A/T]ATGGGAAAACAGGTT	8850
rs532085345	snp	A/C	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20044872	CTAAGCGAATGAACC[A/C]GAGAAGAGAAAATGG	8850
rs532091684	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20104857	GTTCTGAAGAAAAGA[A/G]AAATATAAGTATTCT	8850
rs532122029	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20122413	TGCAGATGAAGGAAC[A/G]TGTGCCTTAATATTT	8850
rs532133428	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20123037	CTCACAGTTGAAGGC[A/G]TCATTCCCAGCTTTT	8850
rs532152001	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20084279	CATCTACTTTCATTT[G/T]ATCTTCCTCCACCTC	8850
rs532221020	in-del	-/A	0.148247	0.228356	intron-variant	KAT2B	GRCh38.p7	3:20044070	GAGAATAGAAAAAGA[-/A]AAAAAAAAAAAGAAA	8850
rs532236949	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20137115	ATGTTCTCAGGTAGC[A/G]TTCTTCCAAATAAGT	8850
rs532258818	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20081248	GCCCAGCTGCTGCCT[C/G]TTCACACTGCAGGGC	8850
rs532297512	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20093225	AAACACTGAGGAAAA[A/G]GTGGCCAATAAAGAG	8850
rs532440286	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20149007	TACTGTTAATGTCAC[C/T]GTATATACTCTTTAT	8850
rs532451143	snp	A/C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20073258	TCCCCCAAAATGTCA[A/C/G]CAAGGCCAGTTTGCT	8850
rs532451597	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20107621	GAGATCATGCCATTG[C/T]CCTCCAGCCTGGGGC	8850
rs532480355	snp	C/T	0.000172539	0.00928653	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20137068	GTTGGTTTCTCACCA[C/T]GCAACACTGTTTTGT	8850
rs532570482	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20060924	CACTCCTGGGCAACA[G/T]AGTGAGACCCTGTCT	8850
rs532589688	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20122164	TTACTGATATCCATA[A/C]AACATGATCTGTAAG	8850
rs532610826	snp	A/G	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20150919	CTTTTAAAACATTAT[A/G]CATATTATATTGGGC	8850
rs532613455	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20049151	AGGTGTGAGCCACCG[C/T]GCCTGGCCGGGCATC	8850
rs532617747	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20079794	GACACAGCCTCCTGA[A/G]TTGAGCCAGCATATT	8850
rs532686765	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20062943	CTGTTATCAAATATA[C/T]GGTTTGCAAATATTT	8850
rs532722114	snp	C/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20128781	GGGAGGCCAAGGTGG[C/G]TGGATCTCCTGAGAT	8850
rs532729533	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20128126	GTTGGACTTTGGGGC[A/G]AGGTACCAGGATACT	8850
rs532767996	snp	A/G	0.00358779	0.0422022	intron-variant	KAT2B	GRCh38.p7	3:20060002	TGGCCTTTTATGATG[A/G]GCTTCTTATGCCGAG	8850
rs532817681	in-del	-/T	0.0101066	0.0703643	intron-variant	KAT2B	GRCh38.p7	3:20152313	CAAAGATTGCTAATA[-/T]TTTTTTTTTCCTGTG	8850
rs532867772	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20120982	CAGCCTCAGACTTTT[A/T]AAAAAAAATCATAAA	8850
rs532888038	snp	C/T	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20099067	GATTCAAGCAAAGAT[C/T]GAAGGTAAAGAATTT	8850
rs532904863	snp	A/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20098324	TCTTAGTGCTTACAA[A/T]TGTGGCGCTGGAGTC	8850
rs532910778	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20054815	TCATGTAACCCAGGA[C/T]TGGCACATACTCACA	8850
rs532932273	in-del	-/TCAG	0.00636936	0.0560724	intron-variant	KAT2B	GRCh38.p7	3:20145671	ATCTCTCAAAATTTC[-/TCAG]TCAGTGTGATGGCTT	8850
rs532958771	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20071926	GATGCAGCTGGTGCC[G/T]TGGAACCTGCAAGGC	8850
rs532978127	snp	A/G	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20149676	TAGCCTACACCCTTT[A/G]AAGTGAACACACATC	8850
rs532980761	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20051327	GCATGTGGGCTGATG[A/G]TGTCACTGCTGGTAG	8850
rs533019284	snp	C/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20142701	ACCTGACAGGGCTTT[C/G]TGGGACATTTGTTTT	8850
rs533076365	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20048721	TAGGAAAAATTGTCA[A/G]CAGTTTCCTACTCTT	8850
rs533114708	snp	A/C	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20112019	TATCCCCTCCTCGTC[A/C]TACCTGAGTCATTGT	8850
rs533127171	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20047935	AATACCTTTTTAAAG[G/T]GATATTTTGTATCAA	8850
rs533151133	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20048866	CTGGGTGCCTTTGGG[C/T]AGCGCCCCCCTTTTC	8850
rs533177720	snp	A/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20133163	CGCATCCTTCCAGGT[A/T]CTTTGGTATTGACAC	8850
rs533239640	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20111876	ATAAATAACAAGATC[A/G]GAAATGACAGAAGAA	8850
rs533243483	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20105525	TGATGCCTGTAATCC[C/T]AGCAACTTTGGGAGG	8850
rs533259050	in-del	-/AT			intron-variant	KAT2B	GRCh38.p7	3:20133881	CTATTGAGGTCGAAC[-/AT]ATCTCTTATATTTAC	8850
rs533290474	snp	A/G	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20076977	GATAGTATCAATTCT[A/G]TTGATTAAATGTTGG	8850
rs533290676	snp	A/G	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20040954	ATTAGCTTCTTCTTG[A/G]ATAAGAGTCCTGCTG	8850
rs533302422	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20092217	AATCTCTACTTTCAC[A/G]TATTTATTTATTTAT	8850
rs533307812	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20104817	AAAGCAGACTGAACA[A/G]TAGTACTGCTTAAAT	8850
rs533307866	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20112810	TAGATTTTTATTATT[C/T]AGATAGTGTTATTAG	8850
rs533330544	snp	A/G	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20096126	GTTGGGTGGGAGGAG[A/G]TGTAGTTGGAGGAGT	8850
rs533380706	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20047316	GGCTCAAGCAATTGG[C/G]CTGCCTTGGCCTTCC	8850
rs533397930	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20147107	ATCATTGGCAATTTT[A/G]TTCAGTTCAAATCCA	8850
rs533406818	snp	C/G	0.00517822	0.0506191	intron-variant	KAT2B	GRCh38.p7	3:20140631	GAGTAGCTAAGATTA[C/G]AGGTGTGTGCTACCA	8850
rs533435980	in-del	-/C	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20135478	GCTAACACAGTGAAA[-/C]CCCGTCTCTACTAAA	8850
rs533477646	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20046150	GCTGGCTAAATAAAC[G/T]GAATTGCCTGGTGCT	8850
rs533496528	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20126437	ATATTGGTTTTGGTA[C/T]CTTAACTAGGTGCCA	8850
rs533554493	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20058859	TCAAACCATCTTTAT[C/G]TCTTCAAATCTTGGC	8850
rs533570499	snp	C/G	1.70388e-05	0.00291875	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20147992	AAACCGAGTGGAAAA[C/G]AGAAAAGGTAAGTAT	8850
rs533598416	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20072228	GACAAAGTCAGGGGT[A/G]AGGGGATAGCTGTCA	8850
rs533660721	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20078686	ATCATCTTTTTCTGA[C/T]ATATGTGTATATATA	8850
rs533700152	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20055987	TCTATTTATTGCTGA[A/G]GAGTATTCTGCTGTA	8850
rs533766160	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20127623	CTGCAGAGCTTGGGA[A/G]GATCTCTCTGTGCCA	8850
rs533767814	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20148954	AGAGGGAGAAATTCT[A/G]CTTACCACAATTCTT	8850
rs533770647	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20057928	TCCAGCATAAACACA[A/G]GGATTTCTTCCAGAC	8850
rs533781324	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20059637	GTGAACCTGGGAGGT[A/G]GAGCTTGCGGTGAGC	8850
rs533792322	snp	A/G	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20041508	GCTCAGTTTGAGGAC[A/G]CCCATTTCTTGCTAC	8850
rs533800874	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20142195	AGCGCAGAGCTATTT[C/T]AGATGGCTAACAAAG	8850
rs533907610	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20120468	CCTGACCTCAGGTAA[A/T]CTACCTGTCTCGGCC	8850
rs533912473	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20094977	GACCAGTCTTGATGC[C/T]ACCAGTACTGATTCT	8850
rs533976077	in-del	-/T			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039289	ACACTGAGTTGAGGG[-/T]TTTTTTTTTCTTTTT	8850
rs533995658	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20065615	TAGCAAATCAAGTAA[C/T]GAGTCCCATATATAT	8850
rs534019189	snp	A/G	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20073806	CTCAGGAAATGTGAC[A/G]TAATAAATGTCTGGA	8850
rs534069051	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20048332	CTGAGAAAGTGTTTT[A/G]CAGGGCAAAACAGCA	8850
rs534074458	snp	A/C	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20054058	CCTCCTCGGCCTCCC[A/C]AAGTGCTGGGATTAC	8850
rs534103535	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20133298	ACTGGAAAAAAACTT[C/T]ACATTGTCCTAGAGA	8850
rs534113485	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20101703	CCACTAGCTATATGA[A/G]CACTTGAAAATGTGG	8850
rs534139182	in-del	-/T			intron-variant	KAT2B	GRCh38.p7	3:20147356	ATTTATCTGTTTTTG[-/T]TTTTTTTTTTTGTAC	8850
rs534139521	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20132261	TGCCTGTAATCCCAG[C/T]TACTCAGAGGCTGAG	8850
rs534173254	in-del	-/TTAT	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20150343	TTTCCCACGATTTCC[-/TTAT]TTGATTTTTCTAATA	8850
rs534221114	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20118445	ATATAGGCCAGGCGT[C/G]GTGGCTGACACCTGT	8850
rs534221610	snp	A/G	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070238	AAAAGGACTCATTCA[A/G]AGGCAGATTTTTCTT	8850
rs534230061	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070746	GGTCACGGTGGCGCA[C/T]GCCTGTAATACCTGC	8850
rs534256541	snp	G/T	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20125543	TCTGTGGATGCTTTT[G/T]CATTATAGCAGAAGA	8850
rs534260124	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20117744	AATTGTCTGTACTGC[C/T]ATGCTGTGTCCTGTA	8850
rs534268438	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20097033	CAGCCATTAGCAGGC[A/G]CTGGACCACTTTAGG	8850
rs534300899	in-del	-/TG	0.00716266	0.059414	intron-variant	KAT2B	GRCh38.p7	3:20099743	ACTTCCTTTAAAGGC[-/TG]TGTGTGTGTGTGTGT	8850
rs534315249	snp	A/T	0.00557542	0.0525036	intron-variant	KAT2B	GRCh38.p7	3:20139285	CTGAAGACAGATAAA[A/T]AATCTCCTATTTATT	8850
rs534394902	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20046044	GAGCCTCAATGACTG[A/C]ATGTATAAAGTGGTG	8850
rs534428051	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20088959	ATTCTTTTGCATGTG[G/T]ATATCCGGTTGTCCC	8850
rs534470944	snp	G/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20109207	TCACGAAATTGAACT[G/T]CTGATTATGAAGATC	8850
rs534490796	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20077150	ATAGTCTGATCAAGT[A/G]GAAAGAACATTCAGT	8850
rs534500908	snp	A/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20083670	GTCTAGGGGGCTATT[A/T]TATTATAGTAGGTTT	8850
rs534502904	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20076254	AATATATATGATCAG[A/G]AAAAGGTCTGGAAGG	8850
rs534538817	snp	C/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20116442	GCACAATGGAATCAC[C/T]CATGGAATTTGAAAT	8850
rs534566854	in-del	-/A	0.0178098	0.0926698	intron-variant	KAT2B	GRCh38.p7	3:20129007	GCGAAACTCCATCTC[-/A]AAAAAAAAAAAAAAA	8850
rs534587274	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20058417	CCGAGATTGCGCCAC[C/T]GCACCGTAGCCTGGG	8850
rs534599177	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20147315	CATAATAGCAACCAT[A/G]TCATTGAATGCCTAC	8850
rs534628169	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20153859	ATCAGCATAAATAAA[A/G]TGGTCATGAATAGTC	8850
rs534629806	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20066948	ATCTCAATTTTTATT[A/G]CCAATTTTTAAAGAC	8850
rs534647154	snp	C/T	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20109604	ATGACTGGTGTAAGC[C/T]ACCATGCCATGCCTA	8850
rs534648776	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20058065	CTTGGGTCATTTCCT[C/T]ATGATATGCTTTCCA	8850
rs534667067	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20081075	TGATAAGCCTTTTGC[A/C]CATTAGTCAATTTGA	8850
rs534674748	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20052699	GAGGCCGGGCACGGT[A/G]GCTCATGCCTGTAAT	8850
rs534714149	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20044632	ACATGCTGTTCACTG[A/G]GACTGGAAGCTCTTC	8850
rs534728013	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20097713	GGCTAATATTTGTAT[A/T]TTTAGTAGAGATGGG	8850
rs534775829	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20125045	ATATATACATGAGGC[C/T]GGGCGCGGTGGCTCA	8850
rs534796402	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20081434	GGTCACTCTCTGGCA[A/C]CCTGGGTGTTTGCAA	8850
rs534805363	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20146651	GCCCCCTTGTAATAG[A/C]TGTTAATATCCACCA	8850
rs534809849	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20091101	TTTAAAGTGTTTGGT[A/T]GAATTCAGCCTTGAA	8850
rs534843076	in-del	-/AA	0.397271	0.202018	intron-variant	KAT2B	GRCh38.p7	3:20062103	ATATATAAAACATAT[-/AA]TATATATTATATAAA	8850
rs534896804	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20144510	TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTCG	8850
rs534936974	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20069370	ATGTAGATTCCCCTG[A/G]TACCCTATCTGGGCT	8850
rs534937504	snp	C/T	0.0394195	0.134744	intron-variant	KAT2B	GRCh38.p7	3:20061938	ATATCATATATAAAA[C/T]ATAATATATATTATA	8850
rs534958498	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20105032	CTAGGATTACAAGTG[C/T]GTGCCACCATGCCTG	8850
rs535006610	snp	C/G			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039006	TGGAAAAAGAAGAAG[C/G]GGAATGTTTCCCACG	8850
rs535024856	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20051437	TGTTGCCACTTGTCC[C/G]TGGTTCTGGAAGATG	8850
rs535027288	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20130146	CCACGCCCGGCCTCA[A/G]CACGAATTATAGCTG	8850
rs535029461	snp	C/T	0.00557542	0.0525036	intron-variant	KAT2B	GRCh38.p7	3:20138317	AAACATAAAAGTTGG[C/T]TCATACTGTGTATAT	8850
rs535048546	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20094087	AGTCTGTCTGAGACT[C/G]TATTAGTTCATTTTC	8850
rs535057132	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20096707	GAGTTCCCTCTTTTG[C/G]TTTGGCTGCTAGGAA	8850
rs535099385	snp	A/C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20132666	GCTAGATACAGAGGA[A/C/G]GTTCAAGTTAAAAGA	8850
rs535108668	in-del	-/TGA	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20080130	AGTGATGATACAATG[-/TGA]TGATCCCATTCTCCT	8850
rs535128758	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20149135	TAATGATTAATTGAA[C/T]CATTTGAGGTCGCTC	8850
rs535187574	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20090623	TATTTTTGCATCCAT[G/T]TTCATCAGGGATATT	8850
rs535236979	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20079754	GATGCCAAAGGACGT[A/C]AACATGGGGCCCAGC	8850
rs535246670	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20108123	CCAAATCCAGTGTGT[A/G]TTTTTCACACATCTT	8850
rs535246698	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20059291	GGTGGCATGCGTCTA[C/G]TAGTCCCAGCTACTC	8850
rs535278266	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20124781	ATATGTTGGTAGCTT[G/T]AAGTTGACTAGCATG	8850
rs535309578	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20071793	CTAAAGCTGGGAGCT[C/G]ACAGAAGTCTTGGAG	8850
rs535425649	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20140790	AGCCATCGCTCCTGG[C/G]CATAGATTTCTTTAA	8850
rs535433768	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20053150	ATCTTATGGCCTGAA[C/T]GTCTCCTACAAATCA	8850
rs535433805	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20047080	TTTGTTTTGCCCCCC[A/C]CTTTTTTTTTTCTGA	8850
rs535444364	snp	A/T	0.00716266	0.059414	intron-variant	KAT2B	GRCh38.p7	3:20052803	TGAAACCCCATGTCT[A/T]CTAAAAAAACAAAAA	8850
rs535447343	in-del	-/T			intron-variant	KAT2B	GRCh38.p7	3:20134509	CGACTCCCTGGTTCA[-/T]GCCGTTCTCCTGCCT	8850
rs535485867	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20075284	AAAAGAAAAAAGAAA[A/G]TATAATAGTATAAAA	8850
rs535510733	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20069572	ACTCTGTCGCTCAGG[C/G]TGGAGTGCAATGGCG	8850
rs535595149	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20110419	CTCATGCCTGTAATC[A/C]CAGCACTTTGGGAAG	8850
rs535620227	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20064057	ATTTCTGGGCTATCT[A/G]TTCTGTTCCATTAGT	8850
rs535665635	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20138414	ACTAGGTGTTTCTTG[G/T]AGGTAATGTGCATGT	8850
rs535665679	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20049699	ATTGAACCTGTGCAG[A/G]CCATAAAGTAAACAA	8850
rs535668165	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20117645	TGCTTGGTTTACTTA[C/T]TTTATTGCCTTCTTG	8850
rs535684955	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20145284	ATTTAAATTACATGC[A/G]TGGCTTGTATTATGT	8850
rs535693449	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20153480	GCAAATGAACATTTT[C/T]CTTTATGTCTCTCCA	8850
rs535719013	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20147663	GCCCAAAATTTGACT[C/T]TCAGTTTAAAAAATA	8850
rs535743443	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20130859	GGATGAGTTTAGTGT[A/G]TGTGTGTGTGTGCGT	8850
rs535760373	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20107408	CACGCCAGTAATCCT[A/T]GCACTTTGGGAGGCC	8850
rs535772753	snp	A/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20045174	CATGCACCACCATAC[A/T]TGGCTAATTTTTGTA	8850
rs535849652	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20131484	AGCACTTCTTCAATA[C/T]GGAGTAAAACTGAAT	8850
rs535850383	snp	G/T	0.00676609	0.0577691	intron-variant	KAT2B	GRCh38.p7	3:20062356	TAATATATAATATAT[G/T]TTATATATAATTTAT	8850
rs535857140	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20123208	TTTTCTTTCTCTCCC[C/G]ACTCCCCATGAACCA	8850
rs535912794	snp	A/G	0.00398564	0.0444627	intron-variant	KAT2B	GRCh38.p7	3:20144579	CAGGCGTGAGCCACC[A/G]AGCCCAGCCAGGTTT	8850
rs535914643	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20152172	GAACTTAAGATTTAA[A/G]AACTGTTTTCCTTGG	8850
rs535920310	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20100738	TGTAGAAAGATTAAA[C/T]TAACAGTTTTTTTAA	8850
rs535986962	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20117210	GTTGCCTGTGACCCT[A/G]TGGGAATTTTATTCG	8850
rs536032855	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20122061	ACATGACTACAAGGA[A/G]AAATAATCAAATCAA	8850
rs536034814	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20130052	TGATGTGATCTGCTC[A/G]CTGCAACCTCCGCCT	8850
rs536050250	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20056962	AACACAAATGCTTGA[C/T]GTTCTTAAGTGGCAT	8850
rs536067541	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20043528	CAGTGGCTGCTAAGA[A/T]CTCTTGGCAGGGCAG	8850
rs536090158	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20080203	TGATCTGTAGTTGAG[C/G]AAGCAGGTTCAGTTC	8850
rs536144728	snp	A/G			utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20153820	GGACAAAGTTTTAAA[A/G]GCGTATTTAACTTGA	8850
rs536167608	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20120479	GTAATCTACCTGTCT[A/C]GGCCTCCCAAAGTGC	8850
rs536208582	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20122081	AATCAAATCAACCAA[C/T]GGTTGAGGCTTTAAA	8850
rs536216026	snp	A/G	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20092788	CTCACTGCAATCTCC[A/G]CCTCCTGGGTTCAAG	8850
rs536229126	in-del	-/T	0.00398564	0.0444627	intron-variant	KAT2B	GRCh38.p7	3:20142394	TGGATTCATGTAGTA[-/T]TTTTTTTCCACAGAA	8850
rs536268003	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20056345	GCCTGAGCAACTGAA[C/T]GGATGGTAGTTCCAT	8850
rs536296846	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20068178	TTTTTGTATTTTTAG[C/T]AGAGATGGGATTTCA	8850
rs536304650	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20136538	CTTTTCATTTGCATC[C/T]TTTTTTTTTCTTCTG	8850
rs536312367	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20062744	TGGGATTACAGGCGT[A/G]AGTCACCGTGCCTGG	8850
rs536317862	in-del	-/AATA			intron-variant	KAT2B	GRCh38.p7	3:20084573	ATATTGCATTATGGT[-/AATA]AATAAATAAATAATT	8850
rs536340002	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20101756	TGATTGTACCAAAAA[G/T]GAGTTTAAAATTGCT	8850
rs536352836	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20093274	CTCACTGTGGGCAAT[C/T]GGTACTCAATTCTGT	8850
rs536390181	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20108992	CTGGTGCCAAAAAAG[C/T]TGGGGACCTCTGCCA	8850
rs536400379	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20100956	GATAGTAAAGCAATA[A/G]TTATTCTGCACAACA	8850
rs536405225	snp	C/G	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20105718	GGGAGGATTGCTTGA[C/G]CCCGGGAGGTCAAGG	8850
rs536407671	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20113864	CATTCACCTATTTAC[A/G]AAGTGTTTTTGTTTT	8850
rs536468467	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20063827	ATTACAGACGTGAGC[C/T]ACCACGCCCGGCCGA	8850
rs536503476	snp	A/G	0.0154538	0.0865337	intron-variant	KAT2B	GRCh38.p7	3:20060612	GTCTAAAAACAAACA[A/G]ACAAACACACAAACA	8850
rs536506830	snp	A/T	0.00557542	0.0525036	intron-variant	KAT2B	GRCh38.p7	3:20074219	CTGGCCTTACTTACG[A/T]TAGTAAAAAGCATGA	8850
rs536604592	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20109556	CTCCTGGGCTCAAGC[C/G]ATCTTCCTGCTTGGG	8850
rs536618650	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20057064	AAGTATTTCTTCTAG[C/T]TGGCTGATAAGGGCC	8850
rs536631123	snp	C/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20055839	CCTTGGAAGCAAGCA[C/G]TGATCTGATTTGTGT	8850
rs536633044	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20049493	GTTACTCATGAAAGC[A/G]TCTGCCCAAGTAGAT	8850
rs536643868	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20135833	AAAGCAGGAATGAGT[C/G]TTTGTAACTCTAGGA	8850
rs536679971	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20143194	GAGAAGAAGATGAGG[A/G]CATACTTTCATTTGG	8850
rs536713617	snp	A/G	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20051581	AATGCCACCTTTCTT[A/G]TGTGGGCCTAGTTGA	8850
rs536716643	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20049881	CCAAATGTGTCAGAA[A/G]GTTAAGAAATTGACT	8850
rs536724087	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20043035	CCTCTTGAGTAGCTG[A/G]GACTACAGGCATGCG	8850
rs536761560	snp	G/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20145476	CCTTTGTGAATGCAA[G/T]TAGTGATTTCTATTG	8850
rs536871303	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20113165	TTGCTCCCAAAATGG[G/T]TTATGAAATTAGGGC	8850
rs536874147	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20074357	CTGAGTTCAAATCCT[A/G]ACTCTATAACCAGTA	8850
rs536892977	snp	A/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20066396	GTTCCAGGGGAACAT[A/G]AACTTTATTTATTAT	8850
rs536914113	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20150405	AAAACTGTTTCTCTC[A/T]TATGGATGGGATCTA	8850
rs536980014	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20116233	GGTTACTGGACATAT[C/T]CTTTGCATTGCTCCC	8850
rs537011857	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20086661	ATGCATATTCCTCAT[C/G]ATGGGTCCATCACTC	8850
rs537012008	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20093966	GTGAATCATTTAGTC[A/G]ACAAAAATATGTTTG	8850
rs537014238	in-del	-/ATTTATTT			intron-variant	KAT2B	GRCh38.p7	3:20045359	TTTATTTATTTATTT[-/ATTTATTT]TAGAGACAGGGTCTT	8850
rs537022485	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20063500	TGGAGTGCAGTGGTG[C/T]GATCTCACCTCACAG	8850
rs537051508	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20044676	AAATTAACTCCCAAC[C/T]CTTCCTATAGAACTC	8850
rs537056403	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20049975	GAGGCTGAGGCAGGC[A/G]GATCGCTTGAGCTCA	8850
rs537071959	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20047259	GAGATGTTTCGCCAA[A/C]CTGGGTTTCGCCATG	8850
rs537076875	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20149449	TGTAGTGAGCTGTGA[C/T]TGCACCACTGCACTT	8850
rs537083875	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20062872	CCCATTGTAAAATTT[C/T]GTTGTTGTTGTTGTT	8850
rs537115729	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20130092	AAGTGATTCTTATGC[C/T]ACAGCCACCTGAGTA	8850
rs537127751	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20095621	TTACACTTGTATGCA[A/G]AGTTGAGTATCTTGG	8850
rs537147599	snp	C/T	0.00438332	0.0466095	intron-variant	KAT2B	GRCh38.p7	3:20125274	AGCGCCACTGCAGTC[C/T]GGCCTGGGCGAAAGA	8850
rs537148064	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20081003	GGCTCTTACTCTTAG[G/T]CTTCTCTTTTTTTTC	8850
rs537155290	in-del	-/G	0.00119737	0.0244387	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038544	TTTAAAAATTTTTGA[-/G]GCAACATTTATATCC	8850
rs537159578	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20087166	GATGACTGTGGTTAA[C/T]AATAATATCTAGTTT	8850
rs537162431	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20153037	TATAGACTTTTTATA[C/T]ATATTTTTTAAAACA	8850
rs537189211	snp	A/G	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20102311	CTCTGTCTCAAAAAA[A/G]AAATTTTTTTTAAAG	8850
rs537202813	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20106921	TCTAGTAGCTACGTA[C/T]AAAATGAATAGATAT	8850
rs537202886	snp	G/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20061394	AGGGATGCTGGGGTT[G/T]CTTGGACCTTCTTGC	8850
rs537217711	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20105204	ATATTGTTACATAAG[G/T]GTATGTTAACTGTAC	8850
rs537224408	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20061226	TCTAAGTGGAATCAT[A/G]CAGTATTTGTCATTT	8850
rs537241449	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20123158	TATGCCACATTTGCT[A/C]CCTCTCTTTCTCTCT	8850
rs537288165	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20067623	GTTTTATAAGCAAGC[C/G]CATAGGAAGAAAAGT	8850
rs537325719	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20093491	GTTGGAAACCAAGAG[C/T]TGTGGTAAGGAGGGG	8850
rs537365505	snp	A/G	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20074952	CATGAGTATGATCCC[A/G]TTTTATTACTTTAGA	8850
rs537425266	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20131037	TTTTTTTTTTTGAGA[C/T]GGAGTTTTGCTCTTG	8850
rs537430946	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20129424	CTGTTGCCCAGGCTG[C/G]AGTGCAGTGGTGTGA	8850
rs537446948	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20128267	ACAATTAGTGACACT[G/T]AACTACTGGAAAGGA	8850
rs537453479	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20056208	TTGGGCTAGGGTAGC[A/T]GGAATGGAGGGGTGA	8850
rs537460574	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20042940	GGTCTCACTCTGCCA[C/T]GTAGGCTGGAGTGCA	8850
rs537476516	snp	A/T	0.00676609	0.0577691	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20136643	CAGCAAGTGATCTTT[A/T]AGATTGAGCTAGGAA	8850
rs537500824	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20066907	GTCTTTGAAATTCAG[A/G]GTGTATTTTCAAACA	8850
rs537551995	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20103547	CCTTAGTAGCTGGGA[C/T]TACAGGCACATGCCA	8850
rs537559103	snp	A/G	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20072899	CTTCATTTTATCTTC[A/G]TATTCCTTAGTTTTG	8850
rs537604131	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20099574	GTGTCTGTTGGACCA[A/G]CATGGGTGGCCTAGG	8850
rs537650387	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20048479	TAAACCCAGTTGCCT[C/T]GGTGTTAGCCAGATT	8850
rs537657820	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20114457	ATATATAACTCATAG[C/G]GTTGATGTGAGGATT	8850
rs537665593	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20063469	TTGAGATGGGGTCTC[A/G]CCCTGTTGCTCAGGC	8850
rs537689942	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20060659	CTGGGCATGGTAGCT[C/T]ATGGCCTGTAATCTT	8850
rs537697916	in-del	-/T			intron-variant	KAT2B	GRCh38.p7	3:20129375	TTGTTCTGTACTGTC[-/T]TTTTTTTTTTTTTTT	8850
rs537698793	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20150489	AAGCATGACTTCTTG[C/T]TACCCATGGATGGCT	8850
rs537713460	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20143806	AAATACTGCATGTTT[A/T]CTGTTATAAGTGGGA	8850
rs537727353	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20100777	AATTTTGAATGATAT[A/G]TATATTTTGGTAAGC	8850
rs537773986	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20049254	GAAGATTAAATACTT[A/C]AGGATATATGAAAGT	8850
rs537778307	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20042519	ACTTATGTAATCAAA[C/T]ACCACCTGTTCCACA	8850
rs537824240	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20112569	TTGATGACTTCTCAT[A/G]GAGCAGTAACAGCGA	8850
rs537843528	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20120636	GTAGGAATAACTGCA[A/C]AGTCACATAGCAAAG	8850
rs537957113	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20148977	CAATTCTTGATTTTC[C/T]ATGCCCTTGATGGGT	8850
rs538040224	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20134883	TTTGACTTTTTTTTA[C/T]TTAATATGTCTAAAA	8850
rs538041706	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20118704	GCACTCCAGCCTGGG[C/T]GACAAAAGCGAAACT	8850
rs538048223	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20126770	GAGGTTGTGGTGAGC[C/T]GAGACCGTGCCATTG	8850
rs538055809	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20125665	ACACTGAATATCATC[C/T]GTGTACACATATAAT	8850
rs538110204	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20127701	CCTCTCACTCCAATG[A/G]TCTCCAACCTTTTTG	8850
rs538137150	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20085964	ATTAATTCCTCTCTT[C/T]TTACCTTTTAAAAAT	8850
rs538178876	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20078065	TTTTAGTCCCAGCTA[C/T]TCGGGAGACTAAGGT	8850
rs538198466	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20105138	TGATCTGCCTACCTC[A/G]TCCTCCTAAAGTGCT	8850
rs538245404	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20114615	TGAGGAAGATTAATG[C/T]ATTTCTACTGATGTA	8850
rs538290527	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20073533	AGAAGTCATCACATT[A/G]GAATAACCTTCTGAA	8850
rs538328202	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20091637	ATTTATTGCCATAAG[C/T]TTCTTTCTTAGAACT	8850
rs538418068	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20130930	TGCATGCGTGCGTGT[A/G]TGTGTGTGTTCTAAT	8850
rs538445445	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20128352	TTCTTATGACCTTGT[C/T]CCTAAGGGAAAACAA	8850
rs538445910	snp	G/T	0.00527701	0.0510946	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20040620	CCGCTGCCGCCGGGG[G/T]CTCGGGCGCCTGCGG	8850
rs538450593	snp	A/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20042983	TAGCTCACTGCAGAC[A/T]CAACCTCCCTGGGCT	8850
rs538484381	in-del	-/GCGGCA	0.136506	0.222754	utr-variant-5-prime, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20040197	TGTGCTGTGGCGGCG[-/GCGGCA]GCGGCAGCGGCAGCG	8850
rs538493268	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	KAT2B	GRCh38.p7	3:20071593	TCATAGGTCAGATCA[C/T]TTAAAGAAGGCTACA	8850
rs538527721	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20134804	CAAATGCAAGTCACA[C/T]AAGTAATTTCAAAAT	8850
rs538597743	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20106271	AAAAATGAACGAACT[A/G]TCATTTTGCTTCTTT	8850
rs538646381	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20150283	TCTTGTCCCCAAGAT[C/T]ATCTTGTATTTGAAG	8850
rs538691872	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20151201	GTGATGACATACACT[C/G]TAACCAAGATAGGCT	8850
rs538708147	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20142965	TGGGTGGGGGGATAA[A/G]TTCTTAAATCTTAAT	8850
rs538767462	snp	C/T	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20107222	TTTTAGTAGAGACGG[C/T]GTTTCACCATGTTGG	8850
rs538832270	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20093246	CAATAAAGAGTGAAT[C/T]ACTAAGCCAGCTCTC	8850
rs538848727	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20120440	GCCATATTGGTCAGG[C/T]TGGTCTCAAACTCCT	8850
rs538851963	snp	C/T	0.00128123	0.0252779	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20137528	GTTCCTTCCTTTCTC[C/T]GTTCCTCCCTTCCTT	8850
rs538859468	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20120936	GATATCACTAATTCA[C/T]GCAGAAACTCTTTAC	8850
rs538898468	snp	A/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20066780	AAAAGCCAAAAATTT[A/T]ATTTTATTAATTCTA	8850
rs538925596	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20080084	CTTCTGGAGTTCTTA[C/T]TTCCATTCCTGCATA	8850
rs538932250	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20124479	CAAATCTCATATGAA[C/G]TAACTGAGCAATAAC	8850
rs538937187	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20086578	TGCACTCCAGCTTGG[A/T]TGACCAAGGGAGACC	8850
rs538937457	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20079537	TTAAGGAAGGTCAAG[A/G]GTTAGCTTTAACAAT	8850
rs538960642	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20121341	TGTGAGGAAATAAAT[A/T]AGATCTAGACATCTT	8850
rs538979055	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20098692	AGCAACCAGAATTAT[G/T]TGTATTTAATTTTTA	8850
rs538992298	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20059220	GAGTTCGAGACCAGC[C/T]TGGCCAACATGGTGA	8850
rs539009682	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20054608	GTTGTGTACTCTTGG[C/T]TTGTGCAGCTTTTTG	8850
rs539011477	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20083958	GGGGTTCGGGGAAGA[C/T]TGGAGCTGGAGAAGA	8850
rs539021112	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20060561	AGCTGAGATCACGCC[A/G]TTGCACTCCAGCCTG	8850
rs539026839	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20091256	ACATTTTCAGGAATT[C/T]ACCCATTTCTTTTAG	8850
rs539050987	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20149882	ATTAACTGATTTTTG[C/T]ATCCTCTTCCTCTGG	8850
rs539053498	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20048189	AAAAATGTTTCATTT[A/G]GCAGGCACAATACAA	8850
rs539093709	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20049018	AGGCCCCCGCCACCA[C/T]GCCCGGCTAATTTTT	8850
rs539150266	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20084606	TAATAAATGCAAAAA[A/G]AAATCACAAAACCAC	8850
rs539165869	snp	A/G	0.0130921	0.0798413	intron-variant	KAT2B	GRCh38.p7	3:20092255	TTTATTTGAGATGGA[A/G]TGTTGCTCTGTTGCC	8850
rs539223105	snp	A/T	1.6495e-05	0.0028718	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20119671	TGAGCAGCCAAACGC[A/T]GGGAGCAGCAGTCCT	8850
rs539274332	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20103543	GCCTCCTTAGTAGCT[A/G]GGACTACAGGCACAT	8850
rs539287019	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20064642	GCAGGGTAGAATGAG[G/T]AACCCCAGGCAAGTC	8850
rs539292046	in-del	-/AAATTTGGTAGATATT	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20096896	AGAATTATATTTTTA[-/AAATTTGGTAGATATT]AAATTTGGGGATATT	8850
rs539325453	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20090753	GTTTTTTGAAGTTTT[C/T]TTTTAGAGTTTCACT	8850
rs539326296	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20148886	TCCTTTGAATAATTA[C/T]TCAGGATAATAATGA	8850
rs539330349	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20097673	TCCTGAGTAGCTGGG[A/G]TTACAGGTGTGTGCC	8850
rs539385302	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20056749	TAGTGTCCTTGCCTT[C/T]TAAGAAGGAGGAGGC	8850
rs539408654	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20087871	CCTCAAACTCCTGGG[A/C]TCAAGGGATCCTCTT	8850
rs539433112	snp	A/G	3.92773e-05	0.00443138	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20040739	CGCTCCGCTCCGCGG[A/G]CCAAGAAACTGGAGA	8850
rs539439365	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20133986	AGAAGATATTTATGT[A/G]TTTTTGATATTAAAT	8850
rs539478945	snp	A/G			utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20153220	TAGTACATAACCACT[A/G]TTTTAATAATTATTT	8850
rs539480827	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20128819	TTGAGACCAGCCTGA[C/T]CAATGTGGTAAAACC	8850
rs539484005	snp	A/G	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20126882	TCTCTAATTGAATTT[A/G]TTTTAACATACATAG	8850
rs539507747	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20064121	GTTGTACCTTGTTAC[A/G]TCCCACAAACACTGT	8850
rs539513458	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20154250	TTTTCTAATTTAAAA[A/G]TTAATATTTTCTTAT	8850
rs539571812	snp	C/T	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20041252	GGGTGGAGAAGACTC[C/T]CGGACTCCTGGCGCT	8850
rs539578627	snp	A/T	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20118377	GTGTGTGTATATGTA[A/T]ATATAAAACTTAGGG	8850
rs539592198	snp	A/G	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20087734	TTTTTAAGATTCTAC[A/G]TACAAATAAGATCAT	8850
rs539607931	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20042602	CGCAGCCAAAGTGGG[C/T]TCATGCAGGAACTGT	8850
rs539635715	snp	A/G	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20078936	ATGGAGTGCAGTGGC[A/G]CGATCTCCACGATCT	8850
rs539639324	snp	A/G	0.00398564	0.0444627	intron-variant	KAT2B	GRCh38.p7	3:20045949	CTTGAAAGTCAAGTA[A/G]GAGCAACAGACTCAG	8850
rs539643189	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20139939	CAGTACAAAATTAAA[A/C]CTAATTTTTACTTAA	8850
rs539662025	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20111236	ATGAAGTAGGTATTA[G/T]TGTTGTCCCCATTTT	8850
rs539662794	in-del	-/TT	0.451234	0.14834	intron-variant	KAT2B	GRCh38.p7	3:20131011	TTTAGTTTCCTGGCC[-/TT]TTTTTTTTTTTTTTT	8850
rs539685744	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20053230	CTTCTGCAAGTTACA[A/G]TTAAATTCTTAAGGC	8850
rs539710772	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20124114	TCTTTCCATTTCCTC[C/G]TAGATGTCCAGTCTG	8850
rs539743546	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20075820	TGGGAGACTGAGGCA[C/T]GAGAATCGATTAAAC	8850
rs539759469	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20096828	TTATTAACTTTTGTC[C/T]TTTATTGTACTAATG	8850
rs539773168	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038864	CCTCAAGACTGGACT[A/C]AAGTTGGGAGAGAAT	8850
rs539773579	snp	A/C	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20046563	ACTAGACCTTGTCTC[A/C]AAATAATAATAATAA	8850
rs539788740	snp	A/G			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20069992	AGAGGTGGATGGTTC[A/G]TTACAGAGAATTTCA	8850
rs539792656	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20047564	CACAACCCAGTGTTA[C/T]GACTTCTTCCATCCC	8850
rs539815685	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20095732	GCATGAGGGATAGAA[C/G]AGTGGACAAAACAGA	8850
rs539857799	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20076172	ATCCCAAGGGTTTTA[A/G]GAGCTTGTGACAGGA	8850
rs539872550	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20071273	GTGGCCAGAGGCTAC[C/T]GTACTGGATAGTATA	8850
rs539903348	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20065857	ACCTGGGGCTTGGGG[G/T]TGGAGTCCCTTTATA	8850
rs539965291	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20110570	CCCAGTTGTTTGGCA[A/G]GCTGAGGTAGGAGGG	8850
rs540001750	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20088843	AAGAAGCTTTTTCCT[A/G]TGTTTCCTTCTAGTA	8850
rs540029652	snp	C/G	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20052055	GAATCACATTCATCT[C/G]TAGCATCTAATTGTG	8850
rs540039926	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20047597	AAAGTTTCCTCTTGC[C/T]GTGAGTACCTTTTTT	8850
rs540047931	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20044206	TAGATCTAGGCCAGG[C/T]GCAGTGGCTCAGACC	8850
rs540085364	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20141011	TCTCCAAATACTCCA[A/G]GTGCATCTATTTACT	8850
rs540086356	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20132199	GACCAACATGGTGAA[A/G]CCCCATCTCTACCAA	8850
rs540100087	snp	A/T			intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20136617	ATTCTGAAAACTTTT[A/T]TATTACTATTCAGCA	8850
rs540124143	snp	C/T	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20082788	CCAAAAATCCCTCCC[C/T]ACCAAATACGTAAGC	8850
rs540128886	snp	A/G	0.00180736	0.0300069	intron-variant	KAT2B	GRCh38.p7	3:20040820	GCGGATGGGTGCTAG[A/G]GGCCCAGCCCGCGGG	8850
rs540141592	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20076750	CTTCTTAATTGTTAC[C/T]GACAAAGTACAAGTT	8850
rs540232339	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20118940	AAATGTAACATTGAT[A/G]TAGTATAGTTACCTA	8850
rs540247076	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20052094	TACCTGCTGCTTTGC[A/G]CACTTTTCTCTGCCA	8850
rs540264044	snp	A/C	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20058299	CCCGTCTCTATTAAA[A/C]ATACAAAAATTAGCT	8850
rs540342701	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20106031	CTAGTCTGGACTTTA[A/G]TTAAGTAACTGGGCC	8850
rs540348297	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20058734	GGAAGGATTGTCACA[A/C]AGTGGAGGAAGAAAA	8850
rs540349711	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20052405	ACAAGTTGTACTGGG[A/G]ATTAAATTCCATTAA	8850
rs540367661	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20054593	AATCAGTCCCCATGC[A/G]TTGTGTACTCTTGGC	8850
rs540391271	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20047003	ATAGAATTAACAGAA[G/T]TTGAGAAAGCCTGTT	8850
rs540409483	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039872	GGGGGTCGGATGGGG[A/G]GCCGCGGAGGGGGGA	8850
rs540411852	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20125237	ATGAACCCGGGAGGC[A/G]GAGCTTGCAGTGAGC	8850
rs540420849	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20133619	CTATCATCAGCAATG[G/T]TCTGTTTGGAAATGT	8850
rs540435613	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20124175	TTTAGTAACATTACA[G/T]ATTAGCTGAGTTTAG	8850
rs540467439	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20047220	GCACGTCACCATGGC[C/T]GGCTAATTTTTGTAT	8850
rs540477937	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20116772	CACAAACCCTGGGAA[A/G]TTGGAATTATGATCT	8850
rs540500455	snp	C/T	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20069154	CATTGCGTATGAACA[C/T]GAGAGCACCCAGTGA	8850
rs540503641	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20153702	CATCTGCCATTCCCA[A/G]CTCTGGGAAAACCAA	8850
rs540505451	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20069317	AAGTATGTGGGGAAA[C/G]CAATGGTAGATCAGG	8850
rs540590708	snp	C/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20103650	CTGACCTCAAGCAAT[C/G]CTCCCACCTTGGCCT	8850
rs540637181	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20042902	AAAATTTATTTTAAC[A/G]TCTTTTTTTTTTTTT	8850
rs540679395	snp	A/C	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20115732	AATATAGAACAGTGG[A/C]CTCCTTCCAGACAGA	8850
rs540694916	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20123370	AGCCTGGTTACAATA[C/T]TTTCTAATACAGGGT	8850
rs540705543	snp	A/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20090030	AAAAAAAACGAATGG[A/T]ACTGATCTTTGTGTG	8850
rs540719146	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20044918	GTGATGTTAGCAGTT[A/G]TGGAATTTTAACTTA	8850
rs540731541	snp	C/T			missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20148290	GCACGCTCAAGAGCA[C/T]CCTCCAGCAGGTGAA	8850
rs540773547	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20096372	AGAGCCAGGACTAAC[A/G]ATGTGGGAAGGAAAC	8850
rs540798583	in-del	-/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20091281	TTTTAGATTATCCAA[-/T]TTATTGACATAACTG	8850
rs540831531	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20078976	GCAACTTCCGCCTCC[C/G]AGGTTCAAGCAATTC	8850
rs540850681	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20108382	CCCATCATCAGTGAA[A/C]GCTTTATTGGACAAT	8850
rs540883868	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20072097	GTGTGGGTCAGCTGC[G/T]TGAGCTGTAGCATGC	8850
rs540927159	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20132046	TGAGAATTTATTTGA[A/G]GCTCCTCTCCTGATT	8850
rs540929088	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20069822	GTGTGAGCCACTGCG[C/T]CCGGCCAAGCTTTTC	8850
rs540935641	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	KAT2B, MIR3135A	GRCh38.p7	3:20137937	GCTGTGCTCAGGAGT[C/T]TGAAACAGCCTGGGC	8850
rs540945315	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20097214	AACTGTGCTCCCTGG[C/T]AGCTCCCCACTACCC	8850
rs540958006	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20109911	TAGGTTAATTTTTAA[G/T]GTAGGCAGATGAACT	8850
rs540970670	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20144826	TTTAAGAGGAAGTCT[C/T]GCTCTGTCACCCAGA	8850
rs540988888	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20116539	TGGACATTGGGACTT[C/T]TAAAAAGCTCCCCAG	8850
rs541066627	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20115051	TGAAGTGTAAGTTGC[A/G]GTTCACTGCAACTTA	8850
rs541099049	in-del	-/ATATATATATTTTTTTTTTT			intron-variant	KAT2B	GRCh38.p7	3:20107007	TATATATATATATAT[-/ATATATATATTTTTTTTTTT]TTTTTTTTTTTTTTT	8850
rs541120843	snp	C/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20075401	CTCTCTGAACACTAG[C/T]TGGAGGTCCCATAAT	8850
rs541122675	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20082331	TGAGCCACTGCACCC[A/G]GCCACGGTTTTCTCT	8850
rs541134702	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20074464	GTATTTACCTTGCAG[C/G]ATCATTGTGAGGATT	8850
rs541173123	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20067858	TTTTGTATTTTTAAT[A/G]GAGATGGGGTCTTGC	8850
rs541181905	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20086369	TTTGGGAATCCGAGA[C/T]GGGAGGATCACTTGA	8850
rs541208326	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20050461	ACTCCTGGTAATCCT[C/T]ATTCTGACTTCTATT	8850
rs541252467	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20062503	GTTTTGCTCTGTCAC[C/G]CAGGCTGGAGTGCAG	8850
rs541270175	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20151786	TCTTATTTCATTGAT[A/G]GAGCTTGAAGCAAAT	8850
rs541282096	in-del	-/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20041043	GTAGCTTCGGCATCC[-/G]GAGCTCCCGGGCTAC	8850
rs541282708	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20092942	CCTGACCTTGTGATT[C/T]GACTGCCTCAGCCTC	8850
rs541294090	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20080919	GTCTTTTTAAACACA[A/G]CTACTGGAATACTTA	8850
rs541306874	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20080447	ATAAAGGCCTTCTTA[A/G]AGCTCTGTGGCAATG	8850
rs541362082	snp	C/T	0.0150606	0.0854603	intron-variant	KAT2B	GRCh38.p7	3:20144085	ACAGAGAGCTTAGGA[C/T]GCCTCCCATTCCCAT	8850
rs541374801	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20142618	GGTGGACCAAGAGTG[A/G]AGAGTTAAGTGCTAC	8850
rs541394762	snp	A/G			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20071281	AGGCTACCGTACTGG[A/G]TAGTATATGTAGATG	8850
rs541404255	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20124258	AAGAAATACCTGAGA[C/G]TGGGTAATTTATTTT	8850
rs541441969	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20144369	TCTTGGCTCACTGCA[A/G]GCTCTGCCTCCTGGG	8850
rs541462784	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038462	GAGGCATCCATACAT[A/C]TTATTTTTGATGTAT	8850
rs541465136	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20119175	GGGAGATATTTTGAG[A/G]CTGTATAAATATCTT	8850
rs541492340	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20125039	TTAAGAATATATACA[C/T]GAGGCCGGGCGCGGT	8850
rs541492501	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20117456	ACAAGATACTCAGAT[A/G]TCTTCTGAATCACCA	8850
rs541509230	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20068359	ATTGGCCTTTACTTT[C/G]TGTTGAGCAAGCCAG	8850
rs541521742	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20062765	CCGTGCCTGGCCCAT[G/T]TTCATAATTATTAAT	8850
rs541528535	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20121194	ACAAAAGTGATTTAG[C/T]AAATAATATGTAATA	8850
rs541551604	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20115684	CTGTGTTTTGACAAA[C/T]ACATATACTTGAGTA	8850
rs541567974	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20093542	GCAGCATCCTCTATC[A/C]CAGGCTTCTGACTGA	8850
rs541590012	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20057613	AATTTCTGATAAATT[C/T]TGTGTGTGTGTATTA	8850
rs541595016	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20050007	GAGTTCGAGACCAGC[C/G]TGGGCAACACGGTGA	8850
rs541622725	snp	C/T	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20128811	TCAGGAGTTTGAGAC[C/T]AGCCTGACCAATGTG	8850
rs541634364	snp	G/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20136785	TCAAAGTTAAGAAAC[G/T]CAAGAAAGGGTGTTA	8850
rs541711761	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20131175	TGTCAGCCACCATGC[C/T]CGGCTAATTTTTGTA	8850
rs541746203	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20081838	CCTTTCCCTAGATTT[A/G]CCTATTAGTAACATT	8850
rs541751651	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20086729	TGGGTGGCCTCTACC[G/T]CTCTAATTTTAAGCC	8850
rs541766901	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20138759	TGTACATTGATTTGT[A/G]AGAACTATTAGTATA	8850
rs541769281	snp	C/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20095757	AACAGAGTTCTTCCC[C/T]TCATGCAATATATAT	8850
rs541851556	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20131932	GCACTTTAAAATCTG[C/T]ATATGGTCATTTTGG	8850
rs541882955	snp	A/G	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20108725	GGCTCATTAGGAACC[A/G]GGCTGCACAGCAGGA	8850
rs541909658	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20056834	GTTCTTTGCCAGCTG[A/G]GTGAACTCAGGCAAG	8850
rs541935641	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20110886	CAGTGATGCTGAGGT[A/G]CATTTTTGACTTTGA	8850
rs541936922	snp	A/C	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20068898	GGGCTGTGGATCAGA[A/C]CAACTATTCAGAAAA	8850
rs541948152	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20091699	TTGTATTTCCACTTC[C/T]GTTTGTCTTAAGATA	8850
rs541973043	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20062543	CTCGGCTCATTGTAA[C/T]GTCTGCCTCCTGGGT	8850
rs542001181	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20048292	CCTGCAAAGCCTTCA[G/T]ATTGCAATTTGTAGT	8850
rs542008497	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20044737	GCAGCCTTCCCATTA[G/T]AAATTATCCAAATTC	8850
rs542014418	in-del	-/C/TATAT	0.00164609	0.0286592	intron-variant	KAT2B	GRCh38.p7	3:20061750	ATATATATGAAAAAA[-/C/TATAT]TATATTATACATAAA	8850
rs542029551	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20102065	CTCACACCTGTAATC[C/G]TAGCACTTTGGGAGT	8850
rs542029889	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20085671	ATGCACCACCACACC[C/T]GGCTATTTTTTGTGT	8850
rs542043280	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20126216	CCACCGAATACTACT[A/G]CACCTGTCTTGCTGT	8850
rs542061019	snp	C/G	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20043883	CCCCTTGGCAAGTTA[C/G]ATTAGAGAGATTAGA	8850
rs542078360	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20139415	AGCTGTAACTGTAGT[G/T]CAAAGCATAAGATCT	8850
rs542091239	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20145914	AAGGGAACAGTTCCT[A/G]GTTATGGGAAGTGAA	8850
rs542106322	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20104443	AATTAGGAGAATCAA[C/T]ATTCGGAGTAAAACC	8850
rs542109466	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20052292	ATTATGTTTTAAAAA[A/G]TGATTTCCTATCTGT	8850
rs542150295	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20109126	GAATGTATTCCCGTT[G/T]TTAAGCAAGACATGA	8850
rs542154515	snp	A/G	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20146751	CTATTTTATAAATGG[A/G]GAAATCGAGTTCCAA	8850
rs542161867	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20083772	AGTCTGGTGGCTGGT[A/C]ATGTGTGGAAGGTAA	8850
rs542239913	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20116610	AGACAATTCTCACCT[C/T]ATATTATCCTAGCCC	8850
rs542248177	snp	C/T	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20115748	CTCCTTCCAGACAGA[C/T]TGCCTTGTACTTCTC	8850
rs542263550	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20063230	GCACCACTATGTCCA[C/G]CTAATTTTTAAAATT	8850
rs542279510	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20050109	GAAGGCTGAGGTGGG[A/G]CGACTGCTTGAGCCC	8850
rs542285881	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20067597	TAGCATGCATCTCAG[A/G]GCAAGGCAGAGTTTT	8850
rs542341720	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20057756	CCTGGAGAGGTCACT[C/T]GGATGTAATGAAGGG	8850
rs542366737	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20151976	TCTACTCCATATAGA[C/T]AGAGCCTCTTCTGTA	8850
rs542382038	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20087287	TCACTGTATATTAAA[C/T]GTATCAAAATATTGC	8850
rs542385141	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20045626	CTTCAAAAGAGAAAC[A/G]AAACCCATTGACTAA	8850
rs542420377	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20121443	GAGAATAGAAAGGAG[A/G]AAAAAACTACCATGC	8850
rs542423766	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20122306	TCAATCCATTTTGAC[A/G]TTTTGGTGTCATATG	8850
rs542450907	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20116303	CACCTAACTTTCAAA[C/T]GGCATTTCTTCTGCA	8850
rs542468472	snp	A/T	0.100231	0.200173	intron-variant	KAT2B	GRCh38.p7	3:20075924	AAAAAAAAAAAAAAA[A/T]TTTTTTTCATACGGC	8850
rs542495720	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20150720	GTATTCAGAATTGGT[C/T]ATAGTTATTCAGAAA	8850
rs542513300	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20060749	GAGTAACATAGTAAG[A/G]CCCTGTCTCTACCAA	8850
rs542519013	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20081139	CTAGCCTCGATGCCA[A/C]ATTCCCATGAACAAA	8850
rs542573322	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20067099	TCTTAGTTTTCAGGG[A/G]ATTTTAATTTGTTTG	8850
rs542594670	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20094166	AGGTTTAATTGACTC[A/C]CAGTTCTGCATGGCT	8850
rs542606262	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20100199	TTTGGGGAAGAAAAA[C/G]ATTAAGTAGAACATG	8850
rs542626370	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20085638	GCCTCAGCCTCCCGA[A/G]TCGCTGGGACTACTG	8850
rs542654377	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20143397	ACAGATGTTGGCAAA[A/G]CTGTGGAGAAAAGGG	8850
rs542682432	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20128509	TTGTTTTTTTTTGTT[G/T]CTAATTTATCTTCCC	8850
rs542682519	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20120878	AATATAAGAAGTGCC[A/G]TATATTTAGCATATG	8850
rs542687396	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20135156	TCCAAGTTTTATTCA[A/G]ACTCTCAGTGTTCAG	8850
rs542872221	snp	A/G	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20073115	AGTTTTATGATTAAA[A/G]TATTTAAAAAAATCA	8850
rs542894111	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20059860	GATTTCCATCACCTC[C/T]AAAGGATCCTTGGGT	8850
rs542918107	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20074820	TTCAGGATTTAAATA[A/C]CCTGTGGAGGAGCTT	8850
rs542920356	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20142591	GAGAGAGAAAACTAG[C/T]ATAGTTGGACAGGTG	8850
rs542928956	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20072650	AATGCTGCACTGTGT[C/G]CAGTGACTTTGTCCC	8850
rs542958440	snp	C/G	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20098820	CAGATGCCCCATACT[C/G]ATAATTTGTATGGCA	8850
rs543040071	snp	A/G	6.61081e-05	0.00574888	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	KAT2B, MIR3135A	GRCh38.p7	3:20137013	CCTGAACTTCCTCAC[A/G]TATGCAGATGAATAT	8850
rs543062736	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20144660	TTAAAATAAATAAAT[A/G]GAAAGCACCCATCTA	8850
rs543086342	in-del	-/CT	0.0126979	0.078662	intron-variant	KAT2B	GRCh38.p7	3:20058445	GGGCAACGAGCGAGA[-/CT]CTGTCTCAAAAAAAA	8850
rs543090998	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20049051	ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT	8850
rs543108677	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20126404	ACACTAAGATGTTCT[G/T]CTTTCTTCATAATCA	8850
rs543126021	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	KAT2B, MIR3135A	GRCh38.p7	3:20137761	TCCTGGACTCAAGCA[A/G]TCCACCCACCTCGGC	8850
rs543153468	snp	C/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20079108	ATTTTGCCAAGTTAG[C/G]CACGCTGGTCTCAAA	8850
rs543172358	snp	A/G			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070851	CTGCCTCCACTAAAA[A/G]TACAAAAATTAGCTG	8850
rs543274801	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20134421	GTTGTTGTTTGAGAC[A/G]GAGTCTCGCTCTGTC	8850
rs543285282	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20050923	ATCAAGGAGGTGGCC[A/G]GGTATGGTGGCTCAT	8850
rs543302430	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20054634	TTTTGCGAGGTTTGT[A/G]TGGTATGCAGGAGGT	8850
rs543308542	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20048605	AGTCAGCACATCTGC[C/T]TCTCAGATGAATACT	8850
rs543313230	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20066434	TGAGACAGTCTCACT[C/G]TGTCACCTAGCTGGA	8850
rs543313979	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20141939	AGAGCTGGCTTTCCT[C/T]ATTGTTCTCTCTGGA	8850
rs543342404	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20108353	GTATTGGATAGCAGA[A/G]ACATAGAATCATCCC	8850
rs543376534	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20091750	GTTCTTCTCTGACCC[A/G]TTGGTTGTTCAGGAG	8850
rs543384133	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20051122	TGAGGATGGCTTGAA[A/C]CCAGGAGGCAGAGGT	8850
rs543397686	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20087038	ACCTGCCTTGGCCTT[C/G]CAAAGTGCTGAGATA	8850
rs543445354	snp	A/G	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20056533	CATTCTGAATGCCTC[A/G]TAGATGTCAGTTACT	8850
rs543450431	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20117332	TCTACTGTAATTGCA[A/G]TGTGTTCTCTTGGGG	8850
rs543459351	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20093634	CCTGGCAGATATTCC[A/T]CAATAGCCTTTAGTT	8850
rs543474833	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20114227	CATAGTAATTAATCA[C/G]TGGTTCCAATCCTGA	8850
rs543496960	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20151775	AAGTTTGTTATTCTT[A/G]TTTCATTGATGGAGC	8850
rs543511676	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20150078	CCACCCGTGAAGGTT[A/G]TGAACTTCTCCAGTT	8850
rs543526504	snp	A/G	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20129321	TGCAACAGGCATTCA[A/G]TGTCACGAAGAATTA	8850
rs543604320	snp	A/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20106762	ACCTATCATCTTTGT[A/G]TCAGAAATAATGTCA	8850
rs543615480	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20082796	CCCTCCCCACCAAAT[A/G]CGTAAGCATTTGCAA	8850
rs543630012	in-del	-/TATT	0.00676609	0.0577691	intron-variant	KAT2B	GRCh38.p7	3:20100901	GTAATGTAAAAACAA[-/TATT]TATCTAAGAACTGCA	8850
rs543687638	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20065112	GCATACTATTGACCT[C/T]TAACCCTGGATCCTG	8850
rs543731958	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20135935	CTATATGATGCCTGA[A/G]AATGAATTGGTCTAT	8850
rs543747293	snp	A/G	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20092908	GGTTTCACCATATTG[A/G]ACAGGCTGGTCTCGA	8850
rs543762676	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20061584	AGCCATACCATTTTA[C/T]GTCTTCAGCAGGAAT	8850
rs543786837	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20089193	TTCTTTTTGCTCAAG[A/T]TTGCTTTGGCTATTT	8850
rs543902536	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20113625	ATTTAAGGCTATTGG[A/G]GATTTATACCTACAG	8850
rs543905795	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20136253	CATTAGATTTACACG[C/T]TTTCTGTAAGCTTTG	8850
rs543915152	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20066524	CTGCCTCAGCTTCCC[A/G]AGTAGCTGGGATTAC	8850
rs543925177	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20060383	AAGGCGGGCGGATCA[C/T]CTGAGGTCGGGAGTC	8850
rs543934232	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20067140	GTCATTATGAACAAA[A/G]GAAATAAAAATATAC	8850
rs543945034	snp	A/C	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20102924	GTAACAGCAGATAAC[A/C]TGGAAGAATTGTATA	8850
rs543992531	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20041755	ACTCACACACACTCA[A/C]ACCTCCCTGTATTCT	8850
rs544006542	snp	A/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20040932	GTGCTCTTGTCGCCC[A/G]CGCCCAATTAGCTTC	8850
rs544050888	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20084892	GGGGCTTTGAAAAAG[C/T]AAGCTACTATTTCAA	8850
rs544079052	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20142641	AGTGCTACTTTGTGA[G/T]TGTTGACTCCAAGGG	8850
rs544094900	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20042630	TGTCTCAACTCAGTG[C/T]TTCTGTTCTGGCTTT	8850
rs544096924	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20049650	AATTTATTGTACTCC[A/C]ATTGAGAGGTATGTT	8850
rs544137351	snp	C/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20143259	AAGATATTTTCTAGG[C/G]AGGTGAAGTTAATAC	8850
rs544182518	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20047295	CAGGCTGGTCTTGAA[C/T]TCCTGGGCTCAAGCA	8850
rs544189300	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20105465	AGCTTACCCCCACAC[G/T]GGGGAGATGTTTCAT	8850
rs544230895	in-del	-/A			intron-variant	KAT2B	GRCh38.p7	3:20110035	TGCAGAATAAGATTT[-/A]AAAAAAAAAAGTCAG	8850
rs544232654	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20112776	AAAGATTGATGAAAC[A/C]CTGTTTTGTTTGAGA	8850
rs544245810	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20140551	CCTAGACTGGAGTGC[A/G]GTGGCACTATCTCAC	8850
rs544247799	snp	A/G	1.79683e-05	0.00299731	intron-variant	KAT2B	GRCh38.p7	3:20148513	TAACATTTTCTAAGT[A/G]TAGATTTAAAACTCT	8850
rs544308974	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20150011	AGGTCTAGCAGATCT[C/T]GTCGATCATAGCCTA	8850
rs544309706	snp	C/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20141044	TCTCCAAAGTGTCTT[C/T]GTCCATTAGCCACCC	8850
rs544357990	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20077771	GGCACAATAATATTC[A/G]GTTTACAAAAATTTG	8850
rs544396491	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20119151	TTTAATCAAAAAAAT[A/G]CTTTTGTGGGGAGAT	8850
rs544484354	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20110265	ATAAGAATCTGTGGA[A/G]TAATGCTTTTTGACC	8850
rs544485231	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20119787	CTCCATTACCTGAGG[A/G]GTGCAAAAGGTAGAC	8850
rs544516257	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20088273	GATATATATCCAGAA[C/G]TGGAATTGCTGGGTC	8850
rs544637143	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20060422	ACCTGACCAACAGGG[A/T]GAAACCCTGTCTCTA	8850
rs544661468	snp	G/T	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20055500	CCAGGAAATCCTTCT[G/T]CAGAAGGGACACGGA	8850
rs544664839	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20133752	ACATTTTTCACCAGT[A/G]GTGTTGGAGAGAATA	8850
rs544674920	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20048568	GGTGAAATATAAACT[C/T]TCCTGTAAGATGCCT	8850
rs544723111	snp	C/T	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20060705	TGAGGTGGGAAGATC[C/T]CTTGAGTCCAGGAGT	8850
rs544782242	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20150601	TATTTGGTACCACCA[A/C]TATTTAGTCACCTTT	8850
rs544783539	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20110810	TGTACCCTAGAACTG[C/T]GGTCACATCTCAAGA	8850
rs544841886	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20058779	AGGGAAGGATTACTG[A/G]ACCATTTAATCTGTA	8850
rs544846752	snp	C/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070402	CTTCGCCTCCCAGGT[C/T]CACGCCATTCTCCTG	8850
rs544875716	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20120776	GTTGCATTTCTGTCC[A/G]CAGACTTGACGTCAG	8850
rs544899994	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20076504	TTTTCTGAGATTACT[C/T]TTCCTTCCTCCCTCC	8850
rs544907605	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20097970	CACGGTGGCTCACAA[C/T]TGTAATCCCAGAACT	8850
rs544910473	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20078568	TATCTTTGGTAGAGA[C/T]GGATTTTGTTATATT	8850
rs544913802	snp	G/T	0.000399281	0.0141238	downstream-variant-500B	KAT2B	GRCh38.p7	3:20154525	CTGTTGCATTTGGGG[G/T]AGGTTTCATAAAAAA	8850
rs544923187	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20123596	GCCTAATATAAAACC[A/G]TATTTAAATTTCCCA	8850
rs544948705	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20099104	CAAATTTATTTTCTG[C/T]GTTGTTCTTGGTAAG	8850
rs544970897	snp	C/T	0.00398564	0.0444627	intron-variant	KAT2B	GRCh38.p7	3:20066618	TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA	8850
rs544983010	snp	C/T	6.61102e-05	0.00574898	intron-variant	KAT2B	GRCh38.p7	3:20072495	GGAAAGTATAACGAG[C/T]TCATTGTAGCGTGAG	8850
rs544990261	snp	C/T			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039154	CCTGAGAAAAAGCCC[C/T]GGGCTTTTAAAACCT	8850
rs545012146	snp	A/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20114105	TTTAATTTTTTATTC[A/T]TTTTAAATCACCTGC	8850
rs545016594	snp	A/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20048870	GTGCCTTTGGGCAGC[A/G]CCCCCCTTTTCTTTT	8850
rs545027546	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20091693	GGTATATTGTATTTC[C/G]ACTTCTGTTTGTCTT	8850
rs545055787	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20048504	CAGATTTAATTCTGC[A/G]GTTGTTAAGTAAATC	8850
rs545070985	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20041886	TTATTCTACTAGAAC[A/G]TCTAGGTTATACTCT	8850
rs545089473	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20097891	GTGTCTCATGTGTCA[A/G]TAATTAAAGTAAAAA	8850
rs545120968	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20054164	AGACGGTGTCTCGCT[C/T]TGTCACCTAGGCTGC	8850
rs545124851	in-del	-/TTTG	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20081948	GTCTCTACGTATAAA[-/TTTG]TTTTTCTGGAACTAT	8850
rs545160086	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20072060	CTTCATGGACACCCA[C/T]TGGGGGCAATGGTAG	8850
rs545190101	snp	A/G	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20079045	TATACCACCACACCC[A/G]GCTAATTTTTATAAT	8850
rs545192260	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20118910	CTAACATAAAAACTA[C/T]AGTTTTCTGTCAGCA	8850
rs545200019	snp	A/G	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20106190	TCATCATCATGATGT[A/G]AAAAATCTGGGAGTT	8850
rs545201070	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20119930	ATTGTCATAGCTCAC[G/T]CATTTGGTGTGTTGC	8850
rs545262802	snp	G/T	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20141148	CCAGTTTGATCCACC[G/T]ATTTGAATTTCAGTT	8850
rs545320805	snp	A/G	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20105263	GTTATAGAAAAAAAT[A/G]TGGGCAAATATTTTG	8850
rs545340068	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20149122	ACCACTCTAAAATTA[A/G]TGATTAATTGAATCA	8850
rs545360118	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20082744	CTTTCTAAAAAGATT[A/C]ACATTTTTCTACAAC	8850
rs545401149	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20090892	CTACAGGCATGTGAC[A/G]CCACACCTGCCTAAT	8850
rs545429922	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20048018	GGCTTCAGATAGGCA[A/G]TATTGTCACAGCAAA	8850
rs545457573	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20125754	GTGTATGTGTCTCTG[C/T]GTGTATGTGTGCACA	8850
rs545497088	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20085606	GCCTCCACCTCCTGG[C/G]TTCAAGTGATTCTCT	8850
rs545547643	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20089295	TTGATAGGGATTGCA[C/T]TGAATCTGTAGATCA	8850
rs545571811	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20106554	AAAATAAGATTAATC[A/T]TGGAAGTTAAGAAAA	8850
rs545578029	snp	A/G	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070960	GATGCAGTGAGACAA[A/G]ATCTTGCCACTGCAC	8850
rs545590181	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20077392	GGCCCTGCAGTTTAC[C/T]AAGTTCCTTAACCTT	8850
rs545632255	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20121931	TATTATGGTTTAAGA[C/T]TCATTTGGGGTTGGT	8850
rs545635030	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20096324	TCACATCCATTCCCT[A/G]CTATAGACATACATC	8850
rs545640567	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20053579	GAAGGTATATGAGTG[A/T]TATGAGATCAGTGAG	8850
rs545654310	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20064927	CTTTCTCCTGTTCCT[C/G]TGGATGCCACTCAAA	8850
rs545706544	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20147771	ACATATGGGGCAGCG[C/T]TGTTAGTCTTGGAAA	8850
rs545712185	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20097446	CTGCAAAAAGTATTA[C/T]TCTTGGGCAAATAAG	8850
rs545733770	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20089972	ACATAGTGAGAAGCC[A/G]TCTCTATTAAAAAAC	8850
rs545740476	snp	G/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20059441	AAAAAAAAAAGGCCA[G/T]GCGTGGTGCCTCACG	8850
rs545749694	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20047169	TGGTCCTCCCACCCT[A/G]GTCTCCCAAGTAGCT	8850
rs545755273	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20076664	TTTGTTGTATCTAAC[A/C]CCCTGCTTTTATTTG	8850
rs545795880	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20125105	AGGCGGGCAGATCAC[A/G]AGGTCAGGAGATCGA	8850
rs545821677	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039666	GAGAAAGGGAGAACA[G/T]CACGTCTTTATTTTG	8850
rs545842233	snp	A/C	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20129482	TGGGTTCAAGTGATT[A/C]TCCCACCTCAGCCTC	8850
rs545848025	in-del	-/AAAGA			downstream-variant-500B	KAT2B	GRCh38.p7	3:20154799	AATGATGTCTGTAGG[-/AAAGA]AAAGAATACTATATC	8850
rs545854521	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20058285	CAACATGGTGAAACC[C/T]CGTCTCTATTAAAAA	8850
rs545886111	snp	C/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20108366	GAGACATAGAATCAT[C/T]CCCATCATCAGTGAA	8850
rs545913402	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20064320	TTAGCATGTTCATCA[C/T]CTCAATCACTTGTCA	8850
rs545915273	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152579	GTGTGCCTAAAGCAA[G/T]GTGGTTTAGTTTTTT	8850
rs545916011	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20063751	TTTCACCATGTTGGC[C/T]AGGCTGGTCTTGAAC	8850
rs545963599	in-del	-/T	0.325563	0.238307	intron-variant	KAT2B	GRCh38.p7	3:20119279	GCTGCCAAATAGTGA[-/T]TTTTTTTTTTTTTTT	8850
rs545982322	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20146227	TAAAAAAGACTGTTT[G/T]GTTAGGAAAACATTT	8850
rs545990412	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20045210	TTTGGTAGAGATGGG[A/G]TTTCGCCATGTTTGC	8850
rs545993071	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20067231	GATCTTTATTCAGTT[A/G]CATTTTTAAGCATCA	8850
rs546004998	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20057476	GCCAAAACAACAGGC[A/G]GAAGGGTGAAAAATT	8850
rs546020610	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20148019	GTATGACGGGCAAGA[C/G]GATGTTAATGGAAGT	8850
rs546089029	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039082	GCATAAAATCTGATA[A/G]TAAGCACATTATGAC	8850
rs546184627	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20104098	TGTATAATTGAGTGA[A/G]TGTGTAATTATTTGA	8850
rs546219316	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20117315	GGGCTGTCTTCTCTT[C/G]TTCTACTGTAATTGC	8850
rs546221299	snp	C/T	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20109492	TGGCTGATTTTTAAA[C/T]TTTTTGTAGAGATGG	8850
rs546257167	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20083394	AGGGTTTCTTTTAAT[A/G]ATGAATGACTCTTTT	8850
rs546281211	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20153593	CCAGGGTCATAACCC[C/T]CTAAAATCCATCATG	8850
rs546353196	snp	A/G	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20123329	TCTTACATAACCACA[A/G]TGCAGTCATTACTCT	8850
rs546384521	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20081640	AAGGGTTGGTCAATC[G/T]TGGGTAATTAGTGTA	8850
rs546396880	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20115859	AATGTCATAGGAGTG[A/G]AATCATATAGTAGAT	8850
rs546416311	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20131002	AGTTCTTCCTTTAGT[G/T]TCCTGGCCTTTTTTT	8850
rs546473643	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20068991	TAAGGGTGGTTTCCT[C/G]TGACTCTACAAAATC	8850
rs546480401	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070556	TGATCCGCCCACCTC[A/G]GCCTCCCAAAGTGCT	8850
rs546484996	snp	C/T	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20116715	AATTGATACATTTAT[C/T]AAGTGCTCAGCTAAG	8850
rs546487680	snp	G/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20075351	GACCAGATGTGTGGG[G/T]TTTTTTTTTCTTCAC	8850
rs546576902	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	KAT2B	GRCh38.p7	3:20154623	TCTTACCCACTCACC[C/T]GCTAAACAATAACAA	8850
rs546588854	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20051380	TTCTCCCCTGGAGTC[C/T]GTATTGGTGAGTCCT	8850
rs546629610	snp	A/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20051894	ACACATGGGGTGTTA[A/T]ATCTATTGCCATTTA	8850
rs546641735	in-del	-/A			intron-variant	KAT2B	GRCh38.p7	3:20134243	GTAAAGGTTTATTTT[-/A]ACCTTACATTTAGAT	8850
rs546650239	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20058423	TTGCGCCACTGCACC[A/G]TAGCCTGGGCAACGA	8850
rs546666371	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20075654	TTACTGGTTTAATAT[A/G]AAGGATACACAGACA	8850
rs546670600	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20053096	TAGTTAAGTGTGTTT[C/T]CCCTTGGTTCATGGC	8850
rs546701638	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20148703	CGTTTAGAGCCCACA[C/T]GAGCTTAACGACACT	8850
rs546749573	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20152111	ATGGTCCCTTTAATG[A/C]TAAAATGGCTGTGAT	8850
rs546756808	snp	A/C	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20117598	AAACCACTGGCTATT[A/C]AGTTAGAAGTGCTAT	8850
rs546843624	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20057681	TACTAGTTTCTAGGC[C/T]CCAGTGTCACCCAGG	8850
rs546844669	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20110412	TTGGTAGCTCATGCC[A/T]GTAATCACAGCACTT	8850
rs546866805	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20064014	GGCACACTTGTCAAA[A/G]TCATTTGACCATTAT	8850
rs546873437	snp	A/C/G	0.00398691	0.0444912	intron-variant	KAT2B	GRCh38.p7	3:20109518	GATGGGCGTCTTACT[A/C/G]TGTTGCCCAGGCTGG	8850
rs546881547	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20133803	CACTGGGTACATAAA[C/G]TGTAAACGTATTTGC	8850
rs546906753	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20056926	ACATGATTTGGACTG[A/C]AATTGCCTTGGAAAG	8850
rs546927484	in-del	-/GGC	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20048915	CTTGCTCTGTCGCCA[-/GGC]TGGAGTGCAGTGGCG	8850
rs546932707	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20088546	GCCATTTGTATGTCT[C/T]CTTTTGAGAAATGTC	8850
rs546998177	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20145256	GCCTTTTAAAAATGC[A/G]GCTAGTAGAAAAATT	8850
rs547015957	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20139025	CAGCTACCTGTGTAA[A/T]TGTGACCTCAGGTGC	8850
rs547035577	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038643	GCTCTTATTAGTATC[C/T]GTTAAATCCATGTTA	8850
rs547036015	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20130539	GCGTAATTTTTATTT[C/T]CAAAGATAGCTATAC	8850
rs547072879	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20132114	GCGTGGTGGCTCACA[C/T]CTGTAATCCCAGCAC	8850
rs547112005	in-del	-/CTTTT			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20069529	CTTTTCTTTTCTTTT[-/CTTTT]TTTTTTTTTTGAGAC	8850
rs547121253	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20122432	GCCTTAATATTTCAT[A/G]TATCTAGTTAAAAAT	8850
rs547134387	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20131361	TTAATGATTAATGAA[A/C]AACTTTTGAGACATC	8850
rs547200670	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20062722	CTGCCTCAGCCTCTC[A/C]AAGTATTGGGATTAC	8850
rs547207503	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20058621	TCCTCTTTTCACTTG[C/T]GTCAGATTTTTAAAG	8850
rs547208557	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20100420	ACTTCCTGCTACATT[A/G]TGATTCCTGGAAAGA	8850
rs547214206	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20101568	TGCCTAGTTATCATT[A/G]TGACTCCATCAATTC	8850
rs547232964	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20136435	TTTAAAATGCTATGT[A/G]TGTGATGATTCAGTT	8850
rs547233796	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20086598	CAAGGGAGACCCTGT[C/G]TTGACACTGCCCCAC	8850
rs547247124	snp	A/T	0.00676609	0.0577691	intron-variant	KAT2B	GRCh38.p7	3:20129968	ACAGTACCCATTTTT[A/T]AAAATTATTATTATT	8850
rs547294534	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20093270	AGCTCTCACTGTGGG[C/T]AATTGGTACTCAATT	8850
rs547295138	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20137142	AAGTTTCTCCCCCAG[C/T]GTTTTCTACTTATAA	8850
rs547341317	snp	G/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20090825	CTGCAACCTCAATCT[G/T]GTGGGGTGGGTTCAA	8850
rs547354115	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20102199	CACGTGACTGTAATC[C/T]TGGCTACTTGGGAGG	8850
rs547387250	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20106794	TCTTAGAGCCTTAGA[C/T]GTTTGCAGATCTCTC	8850
rs547418575	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20145594	TATTAAAGGGATAAC[A/C]TCACTGTCTTGGAAG	8850
rs547520491	snp	A/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20074765	GCCACTGAATCATTT[A/T]GGATTCAACTCCAAC	8850
rs547526666	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20093789	ATACCTAAGAGGATC[A/G]TTCTTGAGGTGCCGC	8850
rs547554150	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20143653	CCCATCAAAGGTAGA[C/T]TGGATAAAGAAAATG	8850
rs547555625	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20079275	AATGGTGCAATCTCG[G/T]CTCACTGCAACTTCT	8850
rs547591339	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20151015	TAGGGCCAATTTCAT[A/T]GTTTTTTTCTTCTTT	8850
rs547613493	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20144261	GTGTCGATTTAAGAG[A/T]TTGCCCTTGGGATTC	8850
rs547716326	snp	A/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20087075	GTGAGCCACTGCGCC[A/T]GGCTGAGATTTTTTA	8850
rs547740647	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20067267	TATTGTATGGTAGAA[C/T]TCATTAAGCACTCTA	8850
rs547743340	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20113810	TCTTCATATGTGCTG[C/T]CTTTTTTTCCACTTG	8850
rs547764659	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20116858	TAGACCTTGTAAGTG[A/G]TGGAATTGGGTTTCA	8850
rs547780759	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20072699	GAGTTGGACTGGGGG[A/G]TTGCCAAATAAGATG	8850
rs547824498	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20123386	TTTCTAATACAGGGT[C/T]GGTGAATTACAGCCT	8850
rs547870256	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20076768	CAAAGTACAAGTTGG[G/T]GTCTAGGGAATTCTG	8850
rs547877526	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152969	TTAAGGAAGGGATAC[A/G]TGATTTTAAAAAAGC	8850
rs547889504	snp	A/C/T			intron-variant	KAT2B	GRCh38.p7	3:20047075	TGGTTTTTGTTTTGC[A/C/T]CCCCCCTTTTTTTTT	8850
rs547907621	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20055769	CGTATCAAGACAGAA[C/G]TTTTCCATCCCCCTA	8850
rs547919870	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20061075	GCAATCATCACCACC[A/G]TTCATCCACAGAACA	8850
rs547997199	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20094543	ACCTTAAAAGATGGA[C/T]TGTATTTGAGTAGAA	8850
rs548019135	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20042777	TGAGCATATGTGGCC[A/T]GCATTGATATTTTTG	8850
rs548043146	snp	C/T	0.00438332	0.0466095	intron-variant	KAT2B	GRCh38.p7	3:20121691	ATTTCAAATATATAG[C/T]TATATATACATAATA	8850
rs548065725	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20056770	AGGAGGAGGCACAAG[A/G]TATTTTAGAATGCCA	8850
rs548122938	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20117400	CTGCGTATCGATGCA[A/G]CTGTGATAAATGACA	8850
rs548124412	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20152070	CTTCCTTGTGCTGAA[C/T]AGGGGATTGAACCAG	8850
rs548175574	in-del	-/T	0.204803	0.245881	intron-variant	KAT2B	GRCh38.p7	3:20129376	TTGTTCTGTACTGTC[-/T]TTTTTTTTTTTTTTT	8850
rs548180211	snp	A/G	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20099951	AAAACCTAGCATTGA[A/G]CAGGTAAAAAGATTT	8850
rs548254264	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20065995	CAAAATATGTGGCTT[A/G]AAACAACAAATACAG	8850
rs548257025	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20063447	TCTTTCTTTCTTTTT[C/T]TTTCTTTTGAGATGG	8850
rs548275925	in-del	-/TC	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20106471	CACACACACATTCTG[-/TC]TCTCTCACACACACA	8850
rs548303591	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20093824	TGTTATGTGGCAAAC[A/G]TAGTAATAGATGTTG	8850
rs548304141	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20089729	AGTGTTTTATAGTTT[G/T]CAGTGTACATATCTT	8850
rs548316769	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20087590	ATGATAGTCACCATG[C/T]CACACAATTGATCTC	8850
rs548342133	in-del	-/A			intron-variant	KAT2B	GRCh38.p7	3:20119197	AAATATCTTGTCTTC[-/A]TCAAAATTATACTCA	8850
rs548463730	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20067963	TACCTGTGCCTGTCC[C/T]GTCTGGCTTAATTTC	8850
rs548479473	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20130637	TGAAGGTATTTAATA[C/T]GAATTGGATACTTTG	8850
rs548501456	snp	A/C	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20081338	AGGTTAGTGAGGGTC[A/C]CGGCACACAGTGACA	8850
rs548535276	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20079828	CTTGGCTGGATGTCC[A/G]CTGCTGGCTAATGCA	8850
rs548567741	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20107983	CTGGCTAATGTTTAT[A/C]TTTTTTAGTAGAGAT	8850
rs548570493	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20042465	GGCATACTGCTTGGG[G/T]GATGACTACACCAAA	8850
rs548589485	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20061175	TCGGCAACCACCATT[A/C]CTATCTCTATGAATT	8850
rs548662442	snp	A/G	0.00398564	0.0444627	intron-variant	KAT2B	GRCh38.p7	3:20085845	ATGTAAGTTATTTAT[A/G]TACTTAGAAACAATT	8850
rs548676141	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20056120	TCTGAGAAGAATAAA[A/G]TATATGAGAGAAACA	8850
rs548681103	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20043645	TTGCCTAGGGCCACC[A/G]GCTGGGGTGCGTGGC	8850
rs548722894	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20144377	CACTGCAAGCTCTGC[C/T]TCCTGGGTTCGCACC	8850
rs548802717	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20094570	AGAAGAGATCACAAA[C/G]GGATGAGTGAGGAGA	8850
rs548815222	snp	G/T	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20048886	CCCCCCTTTTCTTTT[G/T]TTTGAGACGGAGTCT	8850
rs548821095	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20054910	CCACTTCTCTGCTAC[A/G]TGTGCAAAAGGAAGC	8850
rs548830211	snp	C/T	0.00597247	0.0543191	intron-variant	KAT2B	GRCh38.p7	3:20115159	CGATGGCTAGATACA[C/T]CTAGGAATCAAGTCT	8850
rs548841919	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20121845	AACAAGCCTGCCAAG[A/G]TTGAATGAGATGAGC	8850
rs548855103	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20079393	TGTTTTTAGTAGAGA[C/T]GGGTTTTATCATGTT	8850
rs548884594	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20150204	TTAAAGCTATAAATG[A/G]TGTTCTTCAGTAGGG	8850
rs548946154	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20120179	CTCTTGAAGCCTAGG[C/T]TTGGAACTTGTAAAC	8850
rs549006529	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20073369	AGTGGGTGACTTCTT[A/C]TGCCATCATTTCTCT	8850
rs549021649	snp	A/G	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20092632	TGTGTATTTACAGTT[A/G]TTATATCCTCTTGAT	8850
rs549026362	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20043261	TAGAGGGTTACCAAC[G/T]GGGTGTCAGGCATTG	8850
rs549027819	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20112232	AACCATCCCTGCCTC[A/T]GCTATAGTAGACTTG	8850
rs549048939	snp	A/G	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20079896	TGGGTCGGGCACAGC[A/G]GGAGTTAAGGGGATA	8850
rs549054085	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20128884	TGGTGGCACATGCCC[A/G]TAGTCCCAGCTGCTT	8850
rs549089376	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20092662	TGAATTGATCCCTTT[A/G]TCATTATATAATGCC	8850
rs549110936	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20086436	AAACTTTGCGCCAAC[A/G]GAAAATACAAAAAAA	8850
rs549135617	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20051949	ATGGGCTGCTTTGGA[A/T]GATTTCTGCTCAGGT	8850
rs549157125	snp	C/G			intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20136492	GTACAGTAAACACTT[C/G]GATTACTAAATATTC	8850
rs549157705	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20106001	AAGAACACTAGGAAA[C/T]AGGAGATCTGACTTC	8850
rs549175687	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20112872	GTTTTAATTCATAAC[A/G]ATAAGTTAGGTTCAA	8850
rs549220204	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20126648	ACCAACATGGAGAAA[A/C]CCCGTCTCTACTAAA	8850
rs549273649	snp	A/C	0.00358779	0.0422022	intron-variant	KAT2B	GRCh38.p7	3:20090952	AAACAGGGTCTCACT[A/C]TGTTGTGCAGGCTTG	8850
rs549276582	snp	A/G	0.00557542	0.0525036	intron-variant	KAT2B	GRCh38.p7	3:20060497	TCCCAGCTACTGGGG[A/G]GGCTGAGGCAGGAGA	8850
rs549332196	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20099220	GCATTGAGATGCCAG[A/C]ACAGTTGGCCTGCAT	8850
rs549355646	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20141295	TTTTTTTATGCATAT[A/G]AATGAAAAGAGAAGC	8850
rs549362567	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	KAT2B	GRCh38.p7	3:20071505	ATGAACCTTTCATAC[A/G]TTGAGACCTGCTGAA	8850
rs549370800	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20078436	GATGTGCAGTGGTGC[A/G]ATCTCAGCTTACTGC	8850
rs549374212	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20041049	TTCGGCATCCGAGCT[C/G]CCGGGCTACCTTGGG	8850
rs549411762	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20043367	TGTGTGTATGCATGT[C/G]TTGGGGGCCTAGGGA	8850
rs549422082	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20102691	GTACCATACAAAATA[C/T]AAGGACCTACATTTA	8850
rs549448713	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20067625	TTTATAAGCAAGCCC[A/G]TAGGAAGAAAAGTTT	8850
rs549485662	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20082178	TAGCTGGGATTACAG[A/G]TGCCTGCCACCATGC	8850
rs549500947	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20072084	ATGGTAGCAAAGTGT[A/G]TGGGTCAGCTGCGTG	8850
rs549501631	snp	A/T	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20122000	CTAATGCAAACTGAT[A/T]TCCGTACATATATGG	8850
rs549532136	snp	A/G	0.0520825	0.152737	utr-variant-5-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20040433	GACCCTGGCGGCGGC[A/G]GCGGCGCCTGACACT	8850
rs549570175	in-del	-/AAAC	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20147152	TATTTAAGCTTTAAT[-/AAAC]AAAATCAAACAAGCA	8850
rs549576486	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20048093	TCAGTCTTTAGCCAC[A/G]TAAGTTTATTGCATA	8850
rs549591389	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20047363	AGGCATGAACCACCA[C/T]GCCTAGCCTAAACCA	8850
rs549599293	snp	A/G	0.00676609	0.0577691	intron-variant	KAT2B	GRCh38.p7	3:20133304	AAAAAACTTTACATT[A/G]TCCTAGAGACCTTTC	8850
rs549603733	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20142891	TCTATGTGCCTGTGT[A/G]TGTGTGTGTGTGTAC	8850
rs549632844	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20104593	TATCTTGATGTTGCT[A/G]TAAGAGAACCTCAGG	8850
rs549637736	snp	A/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20053814	ATTTTATTTTATTTT[A/T]TTGAGATGGAGTCTC	8850
rs549665422	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20143483	GTTTGGAGATTTCTC[A/G]AAGAATTAAAAATAG	8850
rs549665496	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20135481	AACACAGTGAAACCC[C/T]GTCTCTACTAAAAAT	8850
rs549745872	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20054975	ACAGATATTAAGTGA[A/G]AGAAAAATTAAAATG	8850
rs549793368	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20124335	GAATGGCATCAGCAT[A/C]TGCTCAGCTTCTGGG	8850
rs549800789	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20120968	AGTGAGCTTGGATTC[A/G]GCCTCAGACTTTTTA	8850
rs549804569	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20113121	TCTGTGGAGGGAGAT[A/T]CTGAAGCACTTAAAC	8850
rs549818791	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20086515	CTGAGGTCAGAGGAT[C/T]GCTTAAGCTCAGGAG	8850
rs549832464	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20074133	CCTGGCAAATCCATG[A/C]CAGAAATTTAATCTG	8850
rs549860988	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20129622	CTCAGGTGATCTGCC[C/T]TCCCTGGTCTCCCCA	8850
rs549887759	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20080608	TCATTGAATTCAATA[A/T]TGGTAAAATGAGGGC	8850
rs549918233	snp	C/T			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038478	TTATTTTTGATGTAT[C/T]TCAAAGTACAAAGAG	8850
rs549964210	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20092112	AGTATAGTTCAAGCC[A/C]AGTGCTTTGTCATTG	8850
rs549976590	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20084565	GAGATCACATATTGC[A/G]TTATGGTAATAAATA	8850
rs549988442	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20150759	CACCGCCATAATTCT[G/T]GCTTTGTTTCTGCTG	8850
rs550004297	in-del	-/AGATAGATAGATAGAT	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20109284	CTTCCCCTCAGCCCC[-/AGATAGATAGATAGAT]AGATAGATAGATAGA	8850
rs550007454	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20058663	TAAAAATCCCAGCTT[A/G]AAGTCATAGCATTAT	8850
rs550089548	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20141251	TCCTTCTAGGTATTA[A/G]GTGATTTGTTATCTG	8850
rs550129173	in-del	-/TATAT	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20139614	TGTTTATATTATAAA[-/TATAT]TATTTATAATTTTGA	8850
rs550157182	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20134458	CTGGAGTGCGTTGGC[A/G]CGATCTCAGCTCAGA	8850
rs550166293	in-del	-/TTTT	0.497933	0.032082	intron-variant	KAT2B	GRCh38.p7	3:20145555	ATGGGATTTTTTTAG[-/TTTT]TTTTTTTTTTTTTTT	8850
rs550171226	snp	C/G	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20066133	TAGCATCTGGTGGTG[C/G]TTGGCAATCCTTGGC	8850
rs550193914	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20072096	TGTGTGGGTCAGCTG[C/T]GTGAGCTGTAGCATG	8850
rs550220820	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20127336	AGGACATGTCCCTCT[A/T]TCTTAGTTGGTTAAT	8850
rs550295416	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20060543	GAGGCGGAGGTTGCA[G/T]TGAGCTGAGATCACG	8850
rs550295631	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20097638	ACCACCTGAGTTCAA[C/G]TGATTCTCCTGCCTC	8850
rs550302444	snp	C/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20078068	TAGTCCCAGCTACTC[C/G]GGAGACTAAGGTGGG	8850
rs550306113	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20104783	AGCTAACTTGTAAAT[A/G]TTTATTCCATAAAAA	8850
rs550309746	snp	A/G	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20060093	TGCAAGTAATAATCC[A/G]TTATATGACTAGAAC	8850
rs550309818	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20066690	ACAGGCATGAGCCAC[C/T]GCACCTGGCTGGGAC	8850
rs550340698	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20059537	GGTGAAACCCCACCT[C/T]TACTACAAATACAAA	8850
rs550454578	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20096831	TTAACTTTTGTCTTT[C/T]ATTGTACTAATGGGT	8850
rs550471277	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20064579	GTGAGTCCTTCCTCT[C/T]TCACAACCACAGTGC	8850
rs550515150	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20098343	GGCGCTGGAGTCTAA[C/T]TACCTGGGTTTAAAA	8850
rs550545419	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20133616	TTTCTATCATCAGCA[A/G]TGTTCTGTTTGGAAA	8850
rs550555888	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20148750	CGGTAACTGCAGACA[A/G]CACTAGATTTGAAAG	8850
rs550581539	in-del	-/T			intron-variant	KAT2B	GRCh38.p7	3:20129706	GAAACCAAGCATGTA[-/T]TTTACATTTATAACA	8850
rs550584980	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20053214	CCAACCACTGTTTCC[G/T]CTTCTGCAAGTTACA	8850
rs550618127	snp	C/G			utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152916	CATTTTTTTCTAATG[C/G]AATGTGAGAGTTTAC	8850
rs550629935	snp	A/G			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20069977	CTTTGCAACCTCTGA[A/G]GAGGTGGATGGTTCA	8850
rs550637860	snp	C/G	0	0	intron-variant	KAT2B	GRCh38.p7	3:20133922	TTATTCTTGTTCTAG[C/G]CTTTGACAAATTTTC	8850
rs550647126	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070105	AGCTACTCACTGGGG[A/G]ATGTAGCTATGGGGA	8850
rs550650343	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20048179	ATACAAAGGAAAAAA[C/T]GTTTCATTTGGCAGG	8850
rs550681379	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20142030	CTAAAGCCATCACCC[C/T]GCTGTCAGCTGCTCT	8850
rs550691354	snp	A/C			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20071080	CAATATTAATAATAT[A/C]TTTTCTTTAACCCAT	8850
rs550750396	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20125384	TGAATCTGTCATCTC[A/C]AGGGTCCTTAAAGCT	8850
rs550772432	snp	C/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20111134	TTTAATTTTTTCTTT[C/T]ATCTAAACTACCATT	8850
rs550783421	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20076794	TTCTGTTAGGAATTA[C/T]GCAAGCCTGAATTCT	8850
rs550793965	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20083931	TTTGTTGGGATAGGG[A/C]GGATGGAAGGTGGGG	8850
rs550814943	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20104158	AATAGAAAAACAGCA[A/G]AAGAGTCCTTTATAG	8850
rs550816332	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20045934	GGGAGACGCTGTTAA[A/C]TTGAAAGTCAAGTAA	8850
rs550834441	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20083498	TTGACATGGGTTGGG[A/G]TTAATTAGGAGACTG	8850
rs550857426	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20066489	CTGCAACTTTGGCCT[C/G]CTGGGTTCAAGCAAT	8850
rs550879782	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20052044	TTTATAATTTTGAAT[C/T]ACATTCATCTCTAGC	8850
rs550884143	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20147028	TTGTCTGTATGTTAG[A/G]GTTGAGTTGTGTTGG	8850
rs550903421	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20082717	CTTAAAGAACTGCCA[A/G]CGTAGATATGGCTTT	8850
rs550926430	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20063620	CAATCTCAGCTCACT[A/G]CAACCTCTGCCTCCC	8850
rs550931799	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039338	CGATATTTATTCTTT[G/T]GAATTATGCTTATAT	8850
rs550994419	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20054371	TGACCTCGTGATCCA[C/T]CCTCATCGGCCTTCC	8850
rs551011066	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20089558	GGCGTGCGCCACCAT[A/G]CCCGGCTAATTTTTT	8850
rs551044197	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20117672	CTTGGCTGCTGGGAA[C/T]GTCCTTGTTGACTGA	8850
rs551045289	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20085720	TTTGCCACACTAGCC[A/G]GGCTGGCCTCTAACT	8850
rs551049103	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20092063	TCATTGAATGGAATG[C/T]TCTGTATATGTCTGT	8850
rs551101931	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20076146	TAAAAGATACTCCTC[C/T]TGCTCAGGAAATCCC	8850
rs551109497	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20124800	TTGACTAGCATGGCA[C/G]CTGGTTACCTGGATA	8850
rs551110575	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20098358	CTACCTGGGTTTAAA[A/T]CTTTGCTCTATCACT	8850
rs551127317	snp	C/G	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20075093	ACATGGTGAAACCCC[C/G]TCTCTACTAAAAATA	8850
rs551130973	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20142173	AAACCTACAGGGGAA[C/T]GCCAGAAGCGCAGAG	8850
rs551151485	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20042146	GGAAGCTGAGAGTTT[C/G]CATTTCTGACAAACT	8850
rs551181915	snp	A/C	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20057800	TAGGCTATTTGGTAA[A/C]AACTGGAGCCATTCC	8850
rs551183521	snp	A/G	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20095567	TGATTCTCTAAAATG[A/G]CCCACCATAGTTTGA	8850
rs551255769	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20065351	TTAAAGCTGCAAGGC[C/T]AACTCCCTTGGGAGT	8850
rs551258831	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20055620	GAGACCTGTGTGGCT[A/G]GATGGAGGTGGGTGG	8850
rs551268086	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20043713	AGAGTGACATTATCT[C/T]AGATTTGCTTTTTTT	8850
rs551270841	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20059588	CGGGCGCCTGTAGTC[A/C]CAGCTACTTGGGAGG	8850
rs551401998	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20053399	AATTAGCTGGGCATG[A/G]TGGCACATGTCTGTA	8850
rs551407718	snp	A/G	0.0023933	0.0345097	utr-variant-5-prime, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20040094	AGGCTGGCAGCCGCC[A/G]GCACGCACACCTAGT	8850
rs551461655	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20135380	TGATTAGTGGCCGGG[C/T]GCGGTGGCTCACGCC	8850
rs551464502	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20073584	CACAAAAGCAACACA[C/G]TAATAATTTCATCAT	8850
rs551470281	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20126479	GTCTGTGGGCAATTA[C/T]TGGGATATAAGACAG	8850
rs551499444	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20092548	ATTTATTAATGTTTG[A/C]TTTATATTATATTAT	8850
rs551505779	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20134649	CCTGACCTCATGATC[C/T]GCCCACCTCAGCCTC	8850
rs551556885	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20119308	TTTTACTAACTACCA[C/T]AACTCCGTCCTTATT	8850
rs551561749	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20104045	TCTCTAAAACTCAGT[C/T]ACTGCCAATGTGGAG	8850
rs551567120	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20071343	CATGTTATTCTAACA[A/G]TGTATCTTCTGGTTT	8850
rs551601283	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20104886	CTTTTTTTGTTGTTT[G/T]TTTGTTTTTTTTTTT	8850
rs551614320	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20112026	TCCTCGTCCTACCTG[A/T]GTCATTGTCTCTGAC	8850
rs551659856	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20140646	CAGGTGTGTGCTACC[A/G]TGCCCAGCCAATTTT	8850
rs551709679	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20076996	ATTAAATGTTGGGTT[A/T]CTTTTGCCTCAGCCA	8850
rs551735012	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20105553	AGGCTGAGGCGAGAG[A/G]ATCGCTTGAGCCCAG	8850
rs551744674	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20047350	GTGCTGGGATTACAG[A/G]CATGAACCACCACGC	8850
rs551753537	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20110393	AAAATAGGGTTGTCT[A/C]AGTTTGGTAGCTCAT	8850
rs551755484	snp	A/G	0	0	intron-variant	KAT2B	GRCh38.p7	3:20084414	CTATCCTCTTCTGCT[A/G]TGAAAGTTACTCACC	8850
rs551765988	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20109573	TCTTCCTGCTTGGGC[C/G]TTCCAAAGCACTGGG	8850
rs551805950	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20053003	GATGAGGAAACTAAG[A/G]TGCAGGGAGGTTTAG	8850
rs551816790	snp	A/C	0.00676609	0.0577691	intron-variant	KAT2B	GRCh38.p7	3:20083634	TATTTTAGGAAGACT[A/C]CCCTGGCAGCAGAGA	8850
rs551817874	snp	A/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20090577	TTCTTTTAATCTGCT[A/G]TTGAATTCAGATTGC	8850
rs551842867	snp	A/T	0.00159617	0.0282053	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20153057	TTTTTAAAACACTCA[A/T]CTAGATGAGGTGCTT	8850
rs551857053	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20096400	AACTGGTGGTGGAAA[C/T]GGATAGCAAAACTTC	8850
rs551881121	snp	A/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20102315	GTCTCAAAAAAAAAA[A/T]TTTTTTTAAAGGAAA	8850
rs551895509	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20117547	TGGGAGAAAAAAACA[C/T]AGAGCCTGGCACTTT	8850
rs551947830	snp	C/T	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20077922	GCTCACACCTGTAAT[C/T]CTAGCATTTTGGGAG	8850
rs551962213	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20089643	CTGACCTTGTGATTT[A/G]CCTGCCTCAGCCTCC	8850
rs551970109	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20081381	TTCTCAGCAAGGTTG[A/T]CAGCTGCACCGTGAT	8850
rs551987776	snp	A/C	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20052538	TGTGAGATTGGTGGA[A/C]AGGAAACTGTATTGT	8850
rs552050657	in-del	-/AT	0.0130921	0.0798413	intron-variant	KAT2B	GRCh38.p7	3:20125771	TGTATGTGTGCACAC[-/AT]GTGTATTTAGGACTC	8850
rs552058374	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20136784	TTCAAAGTTAAGAAA[C/T]GCAAGAAAGGGTGTT	8850
rs552121457	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20139116	GAGAGAATCTTGCTA[C/T]GTTGCCTGGGCTGGT	8850
rs552172575	snp	A/C	0.00358779	0.0422022	intron-variant	KAT2B	GRCh38.p7	3:20063512	GTGCGATCTCACCTC[A/C]CAGCAACTTCTGAGT	8850
rs552202099	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20103168	TAACAATAGTTCTGT[A/G]TTATTGAAACTCTGC	8850
rs552220030	in-del	-/TATAT	0.0581549	0.160298	intron-variant	KAT2B	GRCh38.p7	3:20061751	ATATATATGAAAAAA[-/TATAT]TATACATAAAAATAT	8850
rs552229596	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20147138	GGTTCTTTTTAGTAT[A/G]TTTAAGCTTTAATAA	8850
rs552268217	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20153846	CTTGATGTTTTCTAT[C/T]AGCATAAATAAAATG	8850
rs552282726	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20103127	TATATCTTCATTTCC[A/G]TATCTTTCATTTTAG	8850
rs552293823	snp	A/G	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20093967	TGAATCATTTAGTCA[A/G]CAAAAATATGTTTGT	8850
rs552295054	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20058387	TTGAACCTGGGAGGC[A/G]GACATTGCAGTGAGC	8850
rs552309171	snp	A/G	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20057898	TAGCAAAGGGAGGGC[A/G]GTTTCTTATTCAACT	8850
rs552318950	snp	A/G	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20122247	AAGAAGACACTGCAC[A/G]TTTACAAAAGATTGG	8850
rs552325286	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20068076	ATCTTGGCTCACTGC[A/G]ACCTCTGCCTCCCGG	8850
rs552336400	in-del	-/TG			intron-variant	KAT2B	GRCh38.p7	3:20121733	ATACACATATGCATA[-/TG]TGTGTGTGTGTGTGT	8850
rs552349255	snp	A/C	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20130686	AGGCAATTCCCCCCC[A/C]TAACCATGTAATTTT	8850
rs552367563	snp	C/T			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038849	TCTGCCATTTCATCC[C/T]CTCAAGACTGGACTC	8850
rs552382654	snp	A/T	0.0023933	0.0345097	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038516	AGAGTTCAATGCTTG[A/T]GATTTTTCTTTTTTT	8850
rs552397432	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20131266	GGTGATCGCCTGCTT[C/T]GGCCTCCCAAAGTGC	8850
rs552446974	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20045449	TTGAACTCCTTGACT[C/T]AGGTGATCCTCCCAC	8850
rs552462665	snp	A/G	0.0345262	0.126772	intron-variant	KAT2B	GRCh38.p7	3:20061923	TAAAATATGTATTAT[A/G]TATCATATATAAAAC	8850
rs552534468	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20094641	AACAAAGATGCAAAA[A/G]TGGGTTTGCAGCTGG	8850
rs552545462	snp	A/G/T	8.24673e-05	0.00642088	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20101378	AAATGTTCCTAAACC[A/G/T]CATCAACTATTGGCA	8850
rs552569202	snp	A/G			intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20137154	CAGTGTTTTCTACTT[A/G]TAAGAACAGGCATTT	8850
rs552577841	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20056916	GGGGAACATAACATG[A/G]TTTGGACTGCAATTG	8850
rs552653308	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20131816	AGATCCTCCCTCCTT[G/T]GCCCCCCAAAGTGCT	8850
rs552658954	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20051417	TAAATATTCATGTGA[A/C]ATCCTGTTGCCACTT	8850
rs552679002	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20042355	AGCCCAGGAGTTGAT[C/T]ATGAAGGGCATTAGA	8850
rs552765704	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20121713	TACATAATATATATG[C/T]ATACATACACATATG	8850
rs552810537	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20152013	TGACTGAATAGCTAA[C/T]AGTAGTCAGTTCATC	8850
rs552820215	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20102447	AGAAAATGTAGAATT[G/T]TGTAGCCTTTATGTC	8850
rs552844014	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20115252	TGGATAGTGAGTGAA[A/G]GCGGCAGTCTTGAGT	8850
rs552891924	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20139348	TTATGGTAAAACTCA[C/T]TGAGAACTTAATTGG	8850
rs552900591	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20074542	ATGATTATTGGCTGA[G/T]GTTGTTCGTAGTAGT	8850
rs552908764	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20081448	ACCCTGGGTGTTTGC[A/G]AGTCTGACACAGCAC	8850
rs552924862	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20128958	GTTGCAGTGAGCCAA[G/T]ATCACAGCACTGCAC	8850
rs552932549	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20088965	TTGCATGTGGATATC[C/T]GGTTGTCCCAACAGC	8850
rs552972107	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20081100	ATTTGACAGATTTCA[A/T]TGTAGTCATTAATTT	8850
rs552997071	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20063586	GTTGCTCTGTTGCCC[A/G]GGCTGGAATGTAGTG	8850
rs553069526	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20082374	TTCAATTACCAACTT[A/T]AGTAAATTTAACATT	8850
rs553115341	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20087680	ACGTTCCAAGTCCCT[A/G]ATAACCATCATTTTA	8850
rs553132146	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20045142	ACCTTAGCCTCCTGA[A/G]TAGCTGAGACCACAG	8850
rs553142149	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20107241	TCACCATGTTGGCCA[A/G]GCTGATCTCGAACTC	8850
rs553151596	in-del	-/T			intron-variant	KAT2B	GRCh38.p7	3:20149843	AATATGTTAAAACTC[-/T]TTTGTGTCCATTTCC	8850
rs553180532	snp	C/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20056391	ATACCATAGGAGAAG[C/G]AGGTTTGGGTAAGAA	8850
rs553205705	in-del	-/T	0.49831	0.0290231	intron-variant	KAT2B	GRCh38.p7	3:20087952	CTAATTAAAAAAAAA[-/T]TTTTTTTTTGTAGAG	8850
rs553225546	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20125561	TTATAGCAGAAGAAG[G/T]AGTAGTTGTGACAAA	8850
rs553266236	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20050887	TGGAAGAACCCAGGA[A/G]GGCAGGAATGTGGAT	8850
rs553301361	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20093543	CAGCATCCTCTATCC[C/G]AGGCTTCTGACTGAG	8850
rs553308313	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20049551	CTCTTCCAAAACTTT[C/T]GCATGGGGTAGAGGG	8850
rs553367742	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20125666	CACTGAATATCATCC[A/G]TGTACACATATAATA	8850
rs553370134	snp	A/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20105603	GCAACAGAATGAGAC[A/T]TCATCTCTACAAAAA	8850
rs553399019	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20097736	GAGATGGGGTTTCAC[A/G]TTGTCGGCCACGCTT	8850
rs553401194	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20120294	GTGCAGTGGTGTGAT[A/C]TCAGCTCACTGCAAC	8850
rs553408801	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20068816	TAGGTTTGGCCTGCC[A/G]TATTTAATTGCTTTG	8850
rs553411519	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20099116	CTGCGTTGTTCTTGG[C/T]AAGTGGCTCTGTGTT	8850
rs553434292	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20130827	ATGAAGATTAGTCTT[C/T]CAAAACAAAATAGAA	8850
rs553434368	snp	G/T	0.00084255	0.0205077	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20122760	GAATTAATCAACGAG[G/T]TTATGTCTACCATCA	8850
rs553444000	snp	G/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20055967	GGATGCATTGGTAGT[G/T]AATTTCTATTTATTG	8850
rs553445964	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20151557	ATAGACAAATGTTAG[C/T]GTCTATTCTAATCTG	8850
rs553488525	snp	A/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20144551	ACCTCGGCCTCCCAA[A/T]GTGCTGGGATTACAG	8850
rs553518327	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20067306	GGTTTCAACACGTGC[A/G]GTTAATATTCAAGAT	8850
rs553520505	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20123176	TCTCTTTCTCTCTGC[A/G]CCTCCCCATATGCTC	8850
rs553531437	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20094208	AGGAATCTTACAATC[A/G]TGGTGGAAGGTGAAG	8850
rs553579927	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20062001	TATAATATATAAAAC[A/T]TATAATATATATTAT	8850
rs553582997	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20128384	GACTAAGGAAATTCT[A/T]TAAGGGAAGTCATGA	8850
rs553614462	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20100917	ATTTATCTAAGAACT[A/G]CATTATATGTGGGCT	8850
rs553622061	in-del	-/T			intron-variant	KAT2B	GRCh38.p7	3:20115926	GCATTTGAGAGGTGA[-/T]TTTTGAAAAAGGTTT	8850
rs553694597	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20067668	TTCTTTCTTTATTTA[C/T]TTTTTTATATTTTTT	8850
rs553695123	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20130149	CGCCCGGCCTCAGCA[C/T]GAATTATAGCTGCTG	8850
rs553777937	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20052113	TTTTCTCTGCCATGT[A/G]TCTCTGTATCTTGTT	8850
rs553785202	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20107223	TTTAGTAGAGACGGC[A/G]TTTCACCATGTTGGC	8850
rs553841004	in-del	-/TTTG	0.00993419	0.0697739	intron-variant	KAT2B	GRCh38.p7	3:20054113	TTAGACTTATTTTTT[-/TTTG]TTTTTGTTTTTTGTT	8850
rs553843143	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20127889	GGTTTGCACTCCTAT[A/G]AGAGTCTAGTGCCAC	8850
rs553867830	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20135142	CATTTGTGTTTTTAT[C/T]CAAGTTTTATTCAAA	8850
rs553873077	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20108131	AGTGTGTATTTTTCA[C/T]ACATCTTAATTCAGT	8850
rs553879350	snp	C/G	0.00478085	0.0486577	intron-variant	KAT2B	GRCh38.p7	3:20092270	GTGTTGCTCTGTTGC[C/G]TAGGCTGGAGTGCAG	8850
rs553929475	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20105307	TCATGATAGTACACT[A/G]TTTAATTCCATGAAG	8850
rs553955299	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20086100	ACATGGTGAAACCCC[A/G]TCTCTACATAAAAAT	8850
rs553971725	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20043008	TGGGCTCAGGTGATC[C/T]TCCTACATCAGCCTC	8850
rs554041901	snp	A/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20065812	TGCTGAGACTATTCT[A/G]TGCTTAAACTGTTAG	8850
rs554094561	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20150335	TTTTACATTTTCCCA[C/T]GATTTCCTTATTTGA	8850
rs554166005	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20073957	TCTCCATTCTAAGCA[C/G]GTAAACACACATGAA	8850
rs554239465	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20050978	GGCCGAGGTGGGCAG[A/T]TCGCTTGAGGCCAAG	8850
rs554243233	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20145335	CTAGATTTACTAGGA[A/G]TATACTTTTACTAGT	8850
rs554257736	snp	A/C/T	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20144580	AGGCGTGAGCCACCA[A/C/T]GCCCAGCCAGGTTTC	8850
rs554276799	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20092770	GCACTGGTGTGATGT[C/T]GGCTCACTGCAATCT	8850
rs554280050	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20152244	AATGTAATCAAACCA[A/C]CAACATAGATTCCTT	8850
rs554309459	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20072156	AACAAAAAGCAAAGC[A/G]CTCAAATCAAATACC	8850
rs554309789	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20078618	TCCTGAGGTCAAGCG[A/G]TCTGCCCACCTCGGC	8850
rs554330735	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20101812	ACATGTAGAAATGAT[A/G]GTACATTGGATACAT	8850
rs554342671	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20085617	CTGGGTTCAAGTGAT[C/T]CTCTTGCCTCAGCCT	8850
rs554344790	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	KAT2B, MIR3135A	GRCh38.p7	3:20137642	CCTGGGCTCAGGTGA[G/T]TCTCCCACCTCAGCC	8850
rs554357486	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20056984	AAGTGGCATTTTAGA[A/G]TACAGTGATGTGAGC	8850
rs554393730	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20110762	GTATGTTGGCCGAAT[A/G]CACTTTCTAAATTAG	8850
rs554394485	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20115485	TATATCTGGCCATGG[A/G]GAAAGACAGGATGCA	8850
rs554452502	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20066289	AGGAAAACGCCAGTC[A/G]TTGGTTTTAGGGCTT	8850
rs554495947	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20060245	TCTTGGGTAGATACT[C/T]AGTGGATTTGCTGGG	8850
rs554523684	snp	A/T	0.00676609	0.0577691	intron-variant	KAT2B	GRCh38.p7	3:20062357	AATATATAATATATT[A/T]TATATATAATTTATA	8850
rs554530221	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20100999	TGTTTCAGGGGTTTT[C/G]ACCTTTTCAGTCCAT	8850
rs554543904	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20092821	ATTCTCCTGCCTCAG[C/T]CTCCTGAGTAGCTAG	8850
rs554644086	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20128510	TGTTTTTTTTTGTTG[C/T]TAATTTATCTTCCCA	8850
rs554658762	snp	C/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20056471	CAAATGCTATTTTGA[C/G]GATAAAATGAAATAA	8850
rs554661538	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20144434	GCTGGGACTACAGGC[A/G]CCCGCCACCATGCCC	8850
rs554673880	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20094367	TGCCTCCATGATCCA[A/G]TCACTTCCCAGCAGG	8850
rs554683099	in-del	-/AGAC	0.00406594	0.0449048	intron-variant	KAT2B	GRCh38.p7	3:20099774	AAGAGAGAGAGAGAG[-/AGAC]AGACAGAAACAGAAG	8850
rs554705464	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20066841	TTATTATAATATGTA[A/G]TCAATATAAAATAAT	8850
rs554730915	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20149182	GCATTGTGTGGGTGA[A/C]AACCAGTTGAAATGT	8850
rs554756539	in-del	-/A			intron-variant	KAT2B	GRCh38.p7	3:20084601	ATAATTAATAAATGC[-/A]AAAAAAAATCACAAA	8850
rs554788722	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20125179	ATACAAAAAATTAGC[C/T]GGGCGCCGTGGCAGG	8850
rs554790187	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20071784	TCTTCATTTCTAAAG[C/T]TGGGAGCTCACAGAA	8850
rs554873227	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20064691	CAGCTTTCTCTTTTA[A/T]TAATGGCAATAATTC	8850
rs554908558	snp	A/G	0.00398564	0.0444627	intron-variant	KAT2B	GRCh38.p7	3:20105722	GGATTGCTTGAGCCC[A/G]GGAGGTCAAGGCTGC	8850
rs554911733	snp	A/G	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20097885	GTTCCTGTGTCTCAT[A/G]TGTCAATAATTAAAG	8850
rs554952931	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20067737	TGGAGTGCAGTGGTG[C/T]GATCTTGGCTCACTG	8850
rs554963740	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20128614	AGTCTGGCGAGAATA[A/G]ACCAGACTCTGAATT	8850
rs555032327	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20049552	TCTTCCAAAACTTTC[A/G]CATGGGGTAGAGGGG	8850
rs555068545	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20136618	TTCTGAAAACTTTTA[C/T]ATTACTATTCAGCAA	8850
rs555118238	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20049919	AAGTTTAGAAGTCCA[A/G]CTGGGCACCGTGGCT	8850
rs555173484	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20149951	TGTGTGACTTTGGGG[A/C]CCTTTCAGCCCCTGT	8850
rs555173803	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20047727	AAGCAATTTGCCTGC[C/T]TCAGCCTCCTGAGTA	8850
rs555178871	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20059350	ACCTGGGAGGCGGAG[G/T]TTGCAGTGAGCTGAG	8850
rs555188946	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20113885	TTTTTGTTTTTGTTT[G/T]TAAGTTGTGTATCTA	8850
rs555246480	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20060632	ACACACAAACAACAA[A/G]CTGTGGTAATGCTGG	8850
rs555262174	snp	C/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20091429	GTCCATTTTTTTTAT[C/G]TTTTCAAAGAACCAA	8850
rs555291764	snp	C/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20055266	AGTGATATATGTCAA[C/G]TTTTTCCGTTTACTC	8850
rs555304200	snp	A/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20054678	GGATGAGACCTGAGT[A/G]ATATCATAGTGATTG	8850
rs555304677	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20049702	GAACCTGTGCAGGCC[A/G]TAAAGTAAACAAAAT	8850
rs555336756	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20150477	ATAGTCTGGCCCAAG[A/C]ATGACTTCTTGTTAC	8850
rs555365147	snp	A/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20085212	TTAAAAAAAAAGTTT[A/G]TAAGACAAAAATAGT	8850
rs555387085	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20109661	AGTGGCCACAGACTA[A/G]CATCTAGCAAACAAT	8850
rs555396777	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20134193	GTATCCCTAAGTTAT[A/G]TGCCCACTTTTCCTA	8850
rs555428888	snp	A/C	0.000264485	0.0114966	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20119720	GGACTTGAGGCAAAC[A/C]CAGGTAAGCTCTTAA	8850
rs555430852	snp	A/C	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20127638	AGATCTCTCTGTGCC[A/C]TGTCCAGAGAAGGTT	8850
rs555433909	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20053456	AGGAGGATCACTTGA[C/G]TCCAGGAGGTCGAGG	8850
rs555437706	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20064729	ACTTACATCGAGTGA[A/G]ATAAGAGTACATGTA	8850
rs555440056	snp	C/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20148970	CTTACCACAATTCTT[C/G]ATTTTCCATGCCCTT	8850
rs555518792	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20120485	TACCTGTCTCGGCCT[C/T]CCAAAGTGCTGGGAT	8850
rs555580686	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20059203	AGATCACTTGAGGTC[C/G]GGAGTTCGAGACCAG	8850
rs555657945	snp	C/T	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20125544	CTGTGGATGCTTTTG[C/T]ATTATAGCAGAAGAA	8850
rs555694083	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20145915	AGGGAACAGTTCCTA[A/G]TTATGGGAAGTGAAG	8850
rs555723375	snp	A/C	0.00159617	0.0282053	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039533	CAGCACTTTCAAACA[A/C]AAATTACAGAGAATA	8850
rs555739759	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20118646	GAGAATAGCTTGAAC[C/T]GGGGAGGCAGAGGAG	8850
rs555788125	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20068854	CATTTAGTCATTTTT[C/G]TTTCTCTAACTTAAG	8850
rs555821830	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20060671	GCTCATGGCCTGTAA[C/T]CTTAGTACTTTGGGA	8850
rs555827139	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20141025	AAGTGCATCTATTTA[C/G]TATTCTCCAAAGTGT	8850
rs555887054	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20066945	CACATCTCAATTTTT[A/T]TTGCCAATTTTTAAA	8850
rs555906565	snp	A/C	0.000115351	0.00759355	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20072392	CTCACCCACTCCCCC[A/C]AGAGCCGACCTGCAG	8850
rs555972995	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20049007	GTTGAGACTACAGGC[C/G]CCCGCCACCACGCCC	8850
rs556041814	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20117767	GTCCTGTATGTGACC[A/G]GTGTTATTGAGAATG	8850
rs556058270	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20042449	AAGGTCATGGGTACA[C/G]GGCATACTGCTTGGG	8850
rs556065970	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20141916	CCTCTCTCTCCCTGT[C/G]TCTCTGAAGAGCTGG	8850
rs556135019	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20077158	ATCAAGTAGAAAGAA[C/T]ATTCAGTTGGGAACT	8850
rs556215054	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20078946	GTGGCGCGATCTCCA[C/T]GATCTCAGCTCACTG	8850
rs556220215	snp	A/G	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20085254	TTATTTCTGTAAATA[A/G]CTGACATAAAAATGT	8850
rs556234194	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20048480	AAACCCAGTTGCCTC[A/G]GTGTTAGCCAGATTT	8850
rs556243128	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20113418	TAAATTTTTTTCCCA[C/T]AACAAATTCATTTTG	8850
rs556329443	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20143840	GAACATTGGGGATAT[A/G]TGCTCACAAAGATGG	8850
rs556384446	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20128347	AAGATTTCTTATGAC[C/T]TTGTCCCTAAGGGAA	8850
rs556391968	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20112405	CAAGGCATAAATGAT[C/G]ATTTAAATATTTTAA	8850
rs556393361	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20054113	TTAGACTTATTTTTT[G/T]TTGTTTTTGTTTTTT	8850
rs556598868	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20134257	TTACCTTACATTTAG[A/T]TTTCTAATCCATTTC	8850
rs556606775	snp	C/G			utr-variant-5-prime, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20040067	GGCCTCCCAGCGCTG[C/G]CAGACACCGTGAGGC	8850
rs556660985	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20091679	ATTTTGTAAGTTTTG[A/G]TATATTGTATTTCCA	8850
rs556682919	snp	A/G	0.00438332	0.0466095	intron-variant	KAT2B	GRCh38.p7	3:20065199	TTTCTTGGTTCTGCA[A/G]TGTCTGCAGAGATGT	8850
rs556753043	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070944	AACCTGAGAGGTGGA[A/G]GATGCAGTGAGACAA	8850
rs556781749	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20133486	TTGCAGGAATTTCTA[C/T]TAATGCTGATATATA	8850
rs556788929	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20104506	ACCACATACCACCAC[A/T]GCATGATGTCTCACT	8850
rs556797555	snp	A/G/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20059307	TAGTCCCAGCTACTC[A/G/T]GGAGGCTGAGGCAGG	8850
rs556806763	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20096281	CCGTAGCTGCCTCTT[C/G]ACTAGTTCTACCTCA	8850
rs556808359	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20083933	TGTTGGGATAGGGAG[A/G]ATGGAAGGTGGGGTT	8850
rs556830966	snp	A/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20154079	AGTTTGGATTAAGTA[A/T]CTTGGACTGGTTTTA	8850
rs556831711	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20093544	AGCATCCTCTATCCC[A/C]GGCTTCTGACTGAGC	8850
rs556849497	snp	A/C			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038372	TTGCGCACTGTGCCC[A/C]TTACCTAGACTCTAT	8850
rs556894709	in-del	-/TTCT			intron-variant	KAT2B	GRCh38.p7	3:20063427	TTTTCTTTTAAGAGA[-/TTCT]TTCTTTCTTTCTTTT	8850
rs556897164	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20068924	GAAAAGCTGGAGGCT[C/T]AGGGAGTTCCTGGAA	8850
rs556914904	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20110483	CGAGACAATCCTGGG[C/T]AACATAGTGAAACCC	8850
rs556941120	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20064811	ATTTTCCATCAACGT[A/G]TTCTTGCTGTGGGAC	8850
rs556954909	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20132717	AACTTGGAATCTGGA[A/G]AAGATTTTTGGAGAG	8850
rs556986174	snp	C/T	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20058519	TTACCTCACTAGTTA[C/T]CTTTTCTCTCTTACA	8850
rs557023441	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20063656	CAAGCAATTCTCCTG[C/T]CTCAGCCTCCCAAGT	8850
rs557033504	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20075750	GGTGCACGACCCCCC[A/T]GGCACCTCCACATGT	8850
rs557034441	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20140796	CGCTCCTGGCCATAG[A/G]TTTCTTTAAAGGTAT	8850
rs557052760	snp	C/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20076559	TTTTCTTAATGGAAA[C/G]TTTCAAACACCCGTA	8850
rs557080749	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20069618	GCAACCTCTGCCGCC[C/T]GGGTTCAAGTGATTC	8850
rs557092783	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20058225	CACTTTGGGAGGCCA[A/C]GGCAGGCAGATCACC	8850
rs557113936	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20047468	AAACAGCTTTATTGC[A/G]GTATAATTTATAGAT	8850
rs557146634	snp	A/G	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20146779	CAAAGCAGTTAGATC[A/G]TTTACTGTTAAAGGG	8850
rs557162117	snp	A/C	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20102501	CATTTCACAGGTTAC[A/C]TTATAGTCCATTGAG	8850
rs557192329	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20105238	ATATATACTCCCAGG[A/G]GCAATTGTGGTTATA	8850
rs557269219	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20140088	TGGTTTTAAGCTAAT[A/C]CTCTTCAGAATAGTA	8850
rs557308247	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20147689	AAATACACAGGCCCA[A/C]AGTACTGTACATATT	8850
rs557347656	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20075303	AATAGTATAAAACTT[C/T]TTTCTATTTTACTCA	8850
rs557352883	snp	G/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20083990	GTTAGCTGGTGATGT[G/T]TATTTGTTGAGAACA	8850
rs557358600	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20131611	TTTGCTCTGTTGCCC[A/G]GGCTGGAGTGCAGTG	8850
rs557378265	snp	A/G	0.00398564	0.0444627	intron-variant	KAT2B	GRCh38.p7	3:20109778	TCACTGTTTCAGACA[A/G]AAGACAACATTAACA	8850
rs557415717	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20153495	CCTTTATGTCTCTCC[A/G]GATAATGTTTATTGT	8850
rs557418198	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20116613	CAATTCTCACCTCAT[A/G]TTATCCTAGCCCCTT	8850
rs557479572	snp	A/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20104303	ATTTCTAGGTGAAAT[A/G]TAGACCAATAGCCCC	8850
rs557516137	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20131873	CCAACCATAAACAGA[C/T]GTTTTAAGTATTTAT	8850
rs557547871	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	KAT2B	GRCh38.p7	3:20071641	TACAAACATAGGGAA[G/T]TGTGAAGAGTATGTG	8850
rs557578915	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20087747	ACATACAAATAAGAT[C/T]ATGCAGTATTTGTCT	8850
rs557588177	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20126910	TAGCCCAGTAGCCTA[C/T]GGGGACTGTGATCCA	8850
rs557588653	snp	A/T	0.00119737	0.0244387	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038312	GGGTTCCCTCCCCCA[A/T]TTGTCACTGTGAAAA	8850
rs557593350	snp	A/G	0.00557542	0.0525036	intron-variant	KAT2B	GRCh38.p7	3:20087306	TCAAAATATTGCTGG[A/G]TACCTCATAAATATG	8850
rs557633986	snp	A/G	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20130875	TGTGTGTGTGTGCGT[A/G]CATGTGTGTGTTTTT	8850
rs557642110	snp	G/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20065421	CATGGGAAAGGTGTT[G/T]TGAAAGGAGACCTCT	8850
rs557661980	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20096909	TAAAATTTGGTAGAT[A/G]TTAAATTTGGGGATA	8850
rs557697989	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20063792	GTGATCCAACTGCTT[C/T]GGCCTCCCCAAGTGC	8850
rs557753935	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20091304	CATAACTGTTCATCA[G/T]AATCTCTTATAATCC	8850
rs557766498	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20047527	GCTTTTGAGTTAATG[C/T]ATGCAGTTGTGCATC	8850
rs557770099	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20048234	AGATGTCCAAATTTA[A/G]TTCTGTATCCTCAGA	8850
rs557777026	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20053281	GTAATCCCAGGTGTG[A/G]GATCCTACTTTTGGG	8850
rs557832958	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20051867	GAATTTACTTAAAGA[C/T]TGTGTGTTTGCACAC	8850
rs557835024	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20064149	TGTATGAGGATTCCA[A/G]TTTTTCACATGCCTG	8850
rs557854001	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20118787	ATATATATATTTATA[C/T]GTTATATATAAATAC	8850
rs557905898	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20052927	GTTGCGGTGAGCTGA[A/G]ATTGCGCCACTGCAC	8850
rs557912223	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20041359	CGCCCTCGGCTGGGG[C/G]CGGAGGCACTGCCGC	8850
rs557962613	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20131652	AGCTCCCTGCGTCTG[C/T]GACCTCCTGTGCTCA	8850
rs558012642	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20141534	TTCCACTTGATACTT[C/T]TGTTATTCGTTTAGT	8850
rs558043009	snp	C/T	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20047204	GGCTACTTGGCCAGG[C/T]GCACGTCACCATGGC	8850
rs558052295	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038902	TTTGCCCTGTCTAAG[C/T]TAATATCACTGTTTA	8850
rs558064202	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20133588	GAAGACATATTTGCT[G/T]ATTTCTGGTAATTTT	8850
rs558105897	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20045981	CCTGAATCCACCCCA[G/T]CTCTGCCACTTGTGT	8850
rs558146150	snp	G/T			intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20136048	CATATGGATTAGGGG[G/T]TTAGATAGAATGACT	8850
rs558161456	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20092757	ACTAGGCTGGAGTGC[A/T]CTGGTGTGATGTCGG	8850
rs558209803	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20139238	TTTTTTTTAAAAATG[C/T]GTTCTTATGTAATTA	8850
rs558224093	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20040931	AGTGCTCTTGTCGCC[C/G]GCGCCCAATTAGCTT	8850
rs558224896	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20147840	GCCATTAATTTCAGT[C/T]GTCTCTCAGAAGTAG	8850
rs558226075	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20131092	GTGATCTCGGCTCAC[A/T]GCAAACTCCGCCTCC	8850
rs558248537	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20138557	CAGCAGTGTATAAGG[A/G]GGTCAGGAAAGGAGT	8850
rs558258334	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20103560	GACTACAGGCACATG[C/T]CACCATGCCTGGCTA	8850
rs558265729	snp	A/C	0.00199481	0.0315187	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20154370	TATTGTACTGGTACA[A/C]AATAGTTTTAAATTA	8850
rs558308911	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20132356	TCAGCCTGGGCAACA[A/C]GAGTGAAACTCCATC	8850
rs558317953	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20116258	GCTCCCTCTGTACCT[C/G]TGCTATTCACTTTAC	8850
rs558379839	snp	A/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20115601	CAAAGAAAAAATGAT[A/T]TATTCTTGCTTTAAA	8850
rs558385395	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20146593	GTTACCCTTTTATGT[A/C]TTCCCTACCACCCAA	8850
rs558387061	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20117321	TCTTCTCTTGTTCTA[C/G]TGTAATTGCAATGTG	8850
rs558403047	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20088857	TATGTTTCCTTCTAG[C/T]AGTTTTACAGTTTCA	8850
rs558403108	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20081642	GGGTTGGTCAATCTT[A/G]GGTAATTAGTGTATA	8850
rs558404561	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20109153	ATGAAAGACATGACC[A/G]TATTAATTCTTACAG	8850
rs558479952	in-del	-/AAAAAAA	0.252983	0.249982	intron-variant	KAT2B	GRCh38.p7	3:20149495	GGGAGACCGTATCTC[-/AAAAAAA]AAAAAAAAAAAAAAA	8850
rs558512124	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20099480	GGCATGTGCCAAGTG[C/T]GTAGGGTTGCATACC	8850
rs558518908	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20095032	TTAGCCACCAGCCCA[C/T]TTTTAACGTTGGGTG	8850
rs558541562	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20101138	CCTCTGGGGATTGCT[A/G]TTTTCTTTTAGGGAA	8850
rs558548501	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20086667	ATTCCTCATCATGGG[C/T]CCATCACTCTGCCTT	8850
rs558557898	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20057107	CTGGCAATGAGAATG[G/T]AGAAGGTATAGATCT	8850
rs558607224	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20151705	CTATATTGGGAAATA[C/T]TCTTTGCAATAGTCT	8850
rs558619149	snp	C/T	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20045282	CTCCACCTCCCAAAG[C/T]GCTGGGATTACAGGT	8850
rs558623605	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20068750	ACTGCTTGGCTTGAA[A/T]TGCTGTTCTCCAAAC	8850
rs558655157	in-del	-/AAAT	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20087390	TAAGGTTTAATTGAC[-/AAAT]AAAAATGTATATATT	8850
rs558657332	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20081010	ACTCTTAGGCTTCTC[C/T]TTTTTTTCATTCCAG	8850
rs558697060	snp	A/C	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20061237	TCATACAGTATTTGT[A/C]ATTTTGTGACTATTT	8850
rs558702169	in-del	-/GC	0.00119737	0.0244387	utr-variant-5-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20040423	CGAGAGGGAGACCCT[-/GC]GGCGGCGGCGGCGGC	8850
rs558715172	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20129460	GCTCACTGCAACCAC[C/T]GCCTCATGGGTTCAA	8850
rs558723548	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20092911	TTCACCATATTGGAC[A/T]GGCTGGTCTCGAACT	8850
rs558736838	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20074409	CTTAATCTGCCTGGA[C/G]CTCAGTTTTTTCAAC	8850
rs558744668	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20139758	TTTGCCTGCAAAGAA[A/G]GGATTTCATTTCCTC	8850
rs558815347	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20073814	ATGTGACGTAATAAA[C/T]GTCTGGACTCAAGAA	8850
rs558816751	snp	A/C/G	0.0138799	0.0821421	intron-variant	KAT2B	GRCh38.p7	3:20068803	TGTTTTTTCCTTCTA[A/C/G]GTTTGGCCTGCCATA	8850
rs558851838	snp	A/G	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20093815	GCCGCCTCCTGTTAT[A/G]TGGCAAACGTAGTAA	8850
rs558875361	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20056555	TCAGTTACTGTTACA[A/G]TTAAAACAATGCTAA	8850
rs558889137	snp	A/C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20131138	CTCCTGCCTCAGCCT[A/C/T]CCGAGTAGCTGGGAT	8850
rs558893024	snp	A/C	0.00676609	0.0577691	intron-variant	KAT2B	GRCh38.p7	3:20099632	TCTTCATAACTCTGG[A/C]CGTGGACATGAAGGC	8850
rs558937992	snp	A/T	0.00213846	0.0326291	intron-variant	KAT2B	GRCh38.p7	3:20062464	TATATATATTTTATT[A/T]TATATATATATATAT	8850
rs558997786	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20049651	ATTTATTGTACTCCA[A/G]TTGAGAGGTATGTTC	8850
rs559032660	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20137453	GAGTTTATAAAAACC[C/T]GCAAACAGTCCTGAT	8850
rs559033251	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20130123	GCCGGGATTACAGGC[A/G]TGAGCCACCACGCCC	8850
rs559061744	in-del	-/TTA			intron-variant	KAT2B	GRCh38.p7	3:20151852	TGTTCACAGATGTAT[-/TTA]TTATCAGTTTCTCTA	8850
rs559083110	snp	C/T	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20130662	ACTTTGTCTTATTAC[C/T]TCCCAGAAAGGCAAT	8850
rs559102634	snp	A/C	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20100117	GGATCAGAGGTGTAT[A/C]CCTAATTTAATACAT	8850
rs559114580	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20044570	AGGGTTCAGGCACAT[A/G]GTTTCCTTTCACCTA	8850
rs559115801	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20045341	TATTTATTTATTTAT[G/T]TATTTATTTATTTAT	8850
rs559200179	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038414	CTATTTGCTTTATCA[C/T]ATCTCTGTTCATCCA	8850
rs559203061	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20049997	TTGAGCTCAGGAGTT[C/T]GAGACCAGCCTGGGC	8850
rs559204829	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20106936	TAAAATGAATAGATA[G/T]AAGAAATTATTCTGA	8850
rs559209293	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20055891	TTTTTCATATAAATG[G/T]TACCACATAGTACAT	8850
rs559235694	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20093504	AGTTGTGGTAAGGAG[A/G]GGGGATATATAGGTG	8850
rs559242365	in-del	-/TT	0.426399	0.208267	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20137541	CCGTTCCTCCCTTCC[-/TT]TTTTTTTTTTTTGAG	8850
rs559272245	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20136656	TTAAGATTGAGCTAG[C/G]AACTTGTGGCCCTGG	8850
rs559294134	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20059273	CAAAAATTAGCCAGG[C/T]GTGGTGGCATGCGTC	8850
rs559310285	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20143809	TACTGCATGTTTTCT[G/T]TTATAAGTGGGAGCT	8850
rs559336230	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20073919	AAAACAGGATCTTCT[G/T]TCTTTCTTAGCCGAG	8850
rs559372360	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20100464	AGGGAATCTGTTAAA[A/G]TGTAAAGAGTTTTTC	8850
rs559384199	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20138652	TGTGAAGTTTGATTT[A/C]TTTTTCCATGTTTAT	8850
rs559387739	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20116785	AAGTTGGAATTATGA[C/T]CTCCTTTACATAGTT	8850
rs559391341	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20081312	TGCAGGCCAATGATA[C/T]ACGGAGCCAGAGGTT	8850
rs559410415	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20091900	TTATTTTTGCACCAA[C/T]CCAATACTTTCCTAC	8850
rs559415186	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20151995	GCCTCTTCTGTATAA[C/T]TCTGACTGAATAGCT	8850
rs559439008	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20107750	AAGGATGTATACTTA[C/T]TTTCTTAGTACTGAG	8850
rs559464325	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20104388	CCACCATCACGTCAT[A/G]TTGATGAGGAAAGGG	8850
rs559464906	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20108514	ATGACAGTAGTCCTT[C/T]AAGATTATGCCAAAA	8850
rs559471468	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20144849	CACCCAGACTGGAGT[A/G]CAATGGCACAACCTT	8850
rs559494548	in-del	-/TTAT	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20045011	ATTGATAGGATTGGG[-/TTAT]TTATTTATTTATTTT	8850
rs559520739	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20079869	TGCCGGTTTCAGAGT[C/T]TTCAGGAGCTGTGGG	8850
rs559527143	in-del	-/AAC	0.0135832	0.0812842	intron-variant	KAT2B	GRCh38.p7	3:20060945	ACCCTGTCTCAAAAC[-/AAC]AACAACAACAACAAC	8850
rs559562635	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20087480	CTAATTAGCATATCT[A/G]TCACCTCACATACTT	8850
rs559599593	snp	A/G			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038840	TGATAAGAATCTGCC[A/G]TTTCATCCCCTCAAG	8850
rs559600149	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20151844	CACTGGTGTGTTCAC[A/G]GATGTATTTATTATC	8850
rs559607899	snp	A/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20115703	TATACTTGAGTAATG[A/G]CCACTGCCATCAAAA	8850
rs559631255	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20068370	CTTTCTGTTGAGCAA[A/G]CCAGGCACTCTCTTG	8850
rs559644814	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20073342	AGTTGCTCTTTCCAC[C/G]TGACCATTATAAGTG	8850
rs559649347	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20067890	ATGTTGGCCAGGCTG[A/G]TCTCGAACTCCTGAC	8850
rs559656841	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20080501	ATATACCAATCTGTA[C/T]TGAACTGTGATTAAG	8850
rs559687058	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20060731	GGAGTTTGAGACCAG[C/T]GTGAGTAACATAGTA	8850
rs559690680	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20051263	TTGGCCAAGTAGATG[C/T]AGATAAGGAATATGA	8850
rs559728786	snp	A/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20115130	CTATTTTCAAACCCA[A/G]TTATAGTCTCAGTCG	8850
rs559753720	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20053948	GATTACAGGCATGTA[C/T]CACCACACCGAGCTA	8850
rs559789904	in-del	-/A	0.245916	0.249967	intron-variant	KAT2B	GRCh38.p7	3:20105801	GCACGACCCTGTCTG[-/A]AAAAAAAAAAAAAAA	8850
rs559814989	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20079639	TAAATCATTTAGGCA[A/G]ATCATTTGACTCAAC	8850
rs559831750	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20063288	CTCAGGCTGGTCTTG[A/G]ACTCCTGACCTTCCC	8850
rs559866912	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20142756	TCTGCATTAGCAGAG[G/T]CTCAGAGTCCAATGG	8850
rs559908203	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20086391	ATCACTTGAGCCCAG[A/G]AGTTCAAGACTAGCC	8850
rs559912905	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20138659	TTTGATTTATTTTTC[C/G]ATGTTTATCAATTCT	8850
rs559934245	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20151364	AATGATGATCCCAAT[G/T]TATTTGGTTATAGGT	8850
rs559956222	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20085750	TCCTGACTTCAGGTG[A/G]TCCACCTGCCTTGGC	8850
rs559996745	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20049160	CCACCGCGCCTGGCC[A/G]GGCATCGCCTTAACT	8850
rs560054222	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20060015	TGGGCTTCTTATGCC[A/G]AGTGTAATGTGTTTG	8850
rs560063656	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20150651	TCAATTGAAAAAACT[C/G]TACGAAGGCCAGAGG	8850
rs560072956	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20134320	AAGGCCTAGCTTAAA[A/C]ATTTCCTTTTCCTCT	8850
rs560165795	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20092975	AAAGTGCTGGGATTA[C/G]AGGTGTGAGCCACCG	8850
rs560173907	in-del	-/T			intron-variant	KAT2B	GRCh38.p7	3:20119279	CTGCCAAATAGTGAT[-/T]TTTTTTTTTTTTTTT	8850
rs560176854	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20099681	AGTTGCCCATTTTAT[C/T]GACTTAAGGATTTGT	8850
rs560230304	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20099164	TTTGAGAGCTTTAAA[C/T]TCCAGTGGCAGGAAT	8850
rs560247612	snp	A/G			intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20136252	ACATTAGATTTACAC[A/G]TTTTCTGTAAGCTTT	8850
rs560313424	snp	A/C	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20041016	AGCCCTTCATTCCTT[A/C]CGCTTGAAAGGAGTA	8850
rs560323418	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20135381	GATTAGTGGCCGGGC[A/G]CGGTGGCTCACGCCT	8850
rs560359668	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20104551	CAAAAATGGGTAATA[C/T]TACTGGCTGCAGGCA	8850
rs560371921	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20048986	CCTGCCTCAGCCTTC[C/G]GAGTAGTTGAGACTA	8850
rs560376745	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20119973	TGATTTCAGCTAGTC[C/T]CACTCAATCTTGGCT	8850
rs560435130	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20050416	AGGACATTTTCAGCA[A/T]CTCAGAGGGTTCTCT	8850
rs560441799	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20105852	GAATACATAGCAAGT[G/T]AGCTAGAACTAACTT	8850
rs560489728	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20085024	ATTGTATACTGATTG[C/G]TTTCATAGCTTATCA	8850
rs560490035	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20077947	TGGGAGGCTGAGGCA[A/G]GTGGATTGTTTGAGC	8850
rs560493449	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20084417	TCCTCTTCTGCTATG[A/G]AAGTTACTCACCCTT	8850
rs560506509	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20097450	AAAAAGTATTATTCT[C/T]GGGCAAATAAGTTAT	8850
rs560562264	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20048569	GTGAAATATAAACTT[C/T]CCTGTAAGATGCCTG	8850
rs560636121	snp	C/T	0.00795532	0.062565	intron-variant	KAT2B	GRCh38.p7	3:20059455	AGGCGTGGTGCCTCA[C/T]GCTTGTAATCCCAGC	8850
rs560646571	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20043982	AGGCCTGATATAAAT[C/T]TGGCCTTTAAACTTC	8850
rs560649021	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20041938	CTCAGTCACAATGGA[A/C]TGTCTATGCTTGCTC	8850
rs560658711	snp	C/T	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20050140	AGGAGGCAGAGATTG[C/T]AGTGAGCTGAGATCA	8850
rs560672814	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20136216	TACTTTTATCTCTCT[G/T]TATGAGGTTCCAAAA	8850
rs560701121	snp	A/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20086441	TTGCGCCAACGGAAA[A/T]TACAAAAAAATTAGC	8850
rs560702041	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20100381	AAAAGCAAAAAAGAA[A/G]TGAGATTTTGTACCC	8850
rs560759901	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20054190	GCTGCAGTGCAGTGG[C/T]GCGATCTTGGCTCAC	8850
rs560768363	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20053640	GCATATATTCTAGAA[G/T]TCTGTATTATATTAG	8850
rs560798079	snp	C/T			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070736	TTATGCTGCTGGTCA[C/T]GGTGGCGCACGCCTG	8850
rs560837241	snp	A/G	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20143452	ATGCAAATTAGTTCA[A/G]CCCCTGTGGAAAGCC	8850
rs560868112	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20041702	GGACTTGGCCTTGTC[A/G]GCTCCTGCGGCCTGT	8850
rs560874071	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20150747	GAAAAGTCCAGACAC[C/T]GCCATAATTCTTGCT	8850
rs560877108	in-del	-/T	0.266819	0.249434	intron-variant	KAT2B	GRCh38.p7	3:20042905	ATTTATTTTAACGTC[-/T]TTTTTTTTTTTTGAG	8850
rs560893880	snp	G/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20116140	GTCCAAAACCTGTAG[G/T]GCTTTGGGGCCTGTC	8850
rs560957354	snp	C/G	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20148689	CATTCTGCAGCTGTC[C/G]TTTAGAGCCCACATG	8850
rs560974776	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20080944	TACTTAAATTTACAT[A/C]TGTGGCTTGCATTAT	8850
rs561010874	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20145506	GTTTTGTTTCGTTTT[G/T]CCAAAATTTCGTTAT	8850
rs561024465	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20067135	TCTCAGTCATTATGA[A/G]CAAAAGAAATAAAAA	8850
rs561033632	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20121475	ATCTCATGAGGAAAG[C/T]GGAAGAAAGTTCTCT	8850
rs561052033	snp	C/G	1.76783e-05	0.00297302	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20136918	CAGTCTAATGTATTT[C/G]TTTGTATACTAACTT	8850
rs561190145	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20098266	CAGTCTTAGATGTTG[A/G]ACATAAACCCAATGG	8850
rs561221656	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20127302	AGGGGCTACATGAAG[A/G]AAGTTTCTATAGAAA	8850
rs561263112	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20119192	TGTATAAATATCTTG[C/T]CTTCATCAAAATTAT	8850
rs561275184	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20121339	CATGTGAGGAAATAA[A/G]TTAGATCTAGACATC	8850
rs561284642	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20060802	TAAAATAAATTATCC[A/C]GGTGTAGAGGTACAT	8850
rs561351783	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20068904	TGGATCAGACCAACT[A/C]TTCAGAAAAGCTGGA	8850
rs561363133	snp	A/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20042607	CCAAAGTGGGCTCAT[A/G]CAGGAACTGTCTCAA	8850
rs561371713	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20071274	TGGCCAGAGGCTACC[A/G]TACTGGATAGTATAT	8850
rs561390446	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20085088	GATGCAGAGGCTCAC[A/G]CCTGTAATCCTAGCA	8850
rs561402478	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20097557	TTTTAACTTTTTTGA[A/G]ACAGAATCTTACTCT	8850
rs561415738	snp	A/G	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20042019	ACTGGTTCAATAAAT[A/G]TTTGTTGAGTGAATG	8850
rs561418456	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20050922	AATCAAGGAGGTGGC[C/G]GGGTATGGTGGCTCA	8850
rs561435772	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20134437	GAGTCTCGCTCTGTC[A/G]CCAGGCTGGAGTGCG	8850
rs561438492	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20043644	GTTGCCTAGGGCCAC[C/T]GGCTGGGGTGCGTGG	8850
rs561485438	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20065120	TTGACCTCTAACCCT[A/G]GATCCTGTTGGGATG	8850
rs561500733	in-del	-/T	0.200156	0.244981	intron-variant	KAT2B	GRCh38.p7	3:20151443	TAGTCAGAAGTGGGG[-/T]TTTTTTTTTTCCCAT	8850
rs561556729	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20049095	TCGATTTCTTGACCT[C/T]GTGATCCGCCCACCT	8850
rs561625344	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20135260	AAGAGGGAGATGATG[A/G]TACTGTTCTGTTTAC	8850
rs561642907	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20104714	TGAAAATGAAGTTAA[A/G]CAGGATTCTTTGTGG	8850
rs561666054	in-del	-/TT/TTT	0.31014	0.242659	intron-variant	KAT2B	GRCh38.p7	3:20144602	CAGGTTTCTTTTTTC[-/TT/TTT]TTTTTTTTTTTTAAG	8850
rs561712753	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20052426	ATTCCATTAAATTTT[C/T]CATTAAATTCATATC	8850
rs561750033	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20053875	ATGATCTCAGCTCAC[C/T]GCGACTTCCATCTCC	8850
rs561764819	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039873	GGGGTCGGATGGGGG[A/G]CCGCGGAGGGGGGAG	8850
rs561793000	snp	C/G	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20148712	CCCACATGAGCTTAA[C/G]GACACTAGACGCAGA	8850
rs561834803	snp	G/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20112724	TTCTGAACTGCTGAT[G/T]TAGAGAATAGAATTT	8850
rs561870494	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20065871	GGTGGAGTCCCTTTA[C/T]AGTCTAGTGCACCAA	8850
rs561882595	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20133681	ATGAATGAATATGGC[C/T]GGTCTAAATTTAAAA	8850
rs561910115	in-del	-/TTTC	0.00279385	0.0372709	intron-variant	KAT2B	GRCh38.p7	3:20067987	TAATTTCATTTCTTT[-/TTTC]TTTCTTTCTTTTTTT	8850
rs561940131	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20102382	TCATTATACATATTA[A/T]CTTCCAGGTTTTGTC	8850
rs561963828	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20118100	TCTCTTTAATTCTCT[C/T]CACTCTTCCCCTAAG	8850
rs562006082	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20090031	AAAAAAACGAATGGT[A/C]CTGATCTTTGTGTGT	8850
rs562016528	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20083884	GAGGAGTTCAGTCTT[G/T]GAGTCATTTTCCGTG	8850
rs562077575	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20140443	TTCCTTGGGTGCTGC[A/G]TGTATGTGTTTACTG	8850
rs562092036	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20153718	CTCTGGGAAAACCAA[C/G]TAATATACAACCATA	8850
rs562103579	snp	A/C	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20096029	GAGGGAGGAACGGGT[A/C]TTTTAGGCCGTGCAC	8850
rs562164282	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20065916	ATGGAGGCCGCATGT[A/T]TTATTTAACATTTTC	8850
rs562173770	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20117419	TGATAAATGACATTC[A/G]TAAGGATGAACCTGA	8850
rs562213463	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20092023	AAAATTTCATGTGCA[C/T]TTGAGAAGAATGTGT	8850
rs562215763	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20069860	TGCATTTTAATAACC[C/G]TTAGGCCAAAGTTGT	8850
rs562216771	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20046398	ACCAGCCTGGGCAAC[A/G]TGGTGAAACCCTGTC	8850
rs562235021	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20048315	TTTGTAGTTTTATAT[A/T]ACTGAGAAAGTGTTT	8850
rs562331744	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20069179	CAGTGAAGAGTAACT[C/G]AAGGAGGTAGTTAGA	8850
rs562394070	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20105504	AGAGTGGCTGTGTGC[A/T]GTAGCTGATGCCTGT	8850
rs562458318	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20076293	TGAGTTGCTGACTGA[G/T]TTTCTCAGGGTACGG	8850
rs562476390	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20065289	CTGCTACAGTAATTG[A/G]CTTGGCAGTGCACTC	8850
rs562531288	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20057865	ACCTTTCAGTCAGCG[A/G]GACCTAATTATAATA	8850
rs562537721	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20071325	GTGACTTCATCTGTG[C/T]TACATGTTATTCTAA	8850
rs562547737	snp	A/C	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20077801	GACAAAGGGATCTAA[A/C]AAAGTGCTTTAGTTG	8850
rs562562672	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20142665	CCAAGGGAAAGGTAG[A/G]ATCTGTAGGGGCCTC	8850
rs562586487	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20054769	ATGCCAAAGATGCCA[A/G]GGTCAGCATACTTTG	8850
rs562628197	snp	G/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20078376	TAGAGGTTTTTTGAT[G/T]ATTTTTCAGTGTTGT	8850
rs562637668	snp	C/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20040936	TCTTGTCGCCCGCGC[C/T]CAATTAGCTTCTTCT	8850
rs562653644	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20040002	GTAGGTGTCGAAGCA[C/G]TGGGGTGGGGGGTGC	8850
rs562659723	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20054242	TCAAGCAATTCTCTG[C/T]CTCAGCCTCCTGAGT	8850
rs562684063	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20116623	CTCATATTATCCTAG[A/C]CCCTTTTTTTCTGTA	8850
rs562708144	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20119180	ATATTTTGAGACTGT[A/G]TAAATATCTTGTCTT	8850
rs562744284	in-del	-/TTGTT			intron-variant	KAT2B	GRCh38.p7	3:20138876	ATAAAATCTATTGAC[-/TTGTT]TTGGTTTGGATTTTG	8850
rs562788511	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20110811	GTACCCTAGAACTGT[A/G]GTCACATCTCAAGAA	8850
rs562788947	snp	C/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20052868	GTAATCCCAGCTATT[C/T]GGGAGGCTGAGGCAG	8850
rs562793052	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20119881	CTTTTGGCTGTACTG[A/G]TTAGTTATTGCTATC	8850
rs562808074	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20114171	TTCCAGATGATTTCT[A/G]TGGGTTGCCAAAACT	8850
rs562828873	in-del	-/A	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20074491	ATTAAATGAGATAAG[-/A]AAAAAATCTTAGAAT	8850
rs562833480	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20140600	GGCCCAAGCAATCCT[C/T]GTACCTCAGCCTCCC	8850
rs562835131	snp	A/G	7.25005e-05	0.00602038	intron-variant	KAT2B	GRCh38.p7	3:20148521	TCTAAGTATAGATTT[A/G]AAACTCTGGATGGCG	8850
rs562838951	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20126385	ATAGCAGTGAGAGAA[C/T]GTAACACTAAGATGT	8850
rs562854757	snp	C/T	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20133148	TTTGTCAGCTTGGTA[C/T]GCATCCTTCCAGGTA	8850
rs562857249	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20133784	TTCCCCCTACCATTG[C/T]TGGCACTGGGTACAT	8850
rs562876463	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20053532	AGAGTGAGACCCTGT[C/T]TCAAAAAACAAGACA	8850
rs562909349	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	KAT2B	GRCh38.p7	3:20154547	CATAAAAAATCCATA[A/G]GTCATCAGTAAGAGA	8850
rs562909900	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20097254	TGAAGGTGGTGTCAA[A/G]GTTTCCATCCTGTCA	8850
rs562938842	snp	G/T	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20084390	TTTATTTCATTCTCA[G/T]AGTAAGAGCTATCCT	8850
rs562968958	snp	C/G/T			intron-variant	KAT2B	GRCh38.p7	3:20140475	ATAGCAAACTCTCGG[C/G/T]TTGCTGTGGGTTATC	8850
rs562987107	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20050981	CGAGGTGGGCAGATC[A/G]CTTGAGGCCAAGAAA	8850
rs563004962	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20110306	TTGGTGCCACCCTCC[A/G]TGGCTACCACTGTTA	8850
rs563006872	snp	A/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20117905	CCTTTTTGTTTGGAA[A/T]TACTGTCAAACTCAC	8850
rs563010278	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20096486	AAAATAAACCTGCTA[C/T]TGAGGGCATTGTAGA	8850
rs563026627	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20052955	CACTCCAGCCTGGGC[A/G]ACAAGAGCTAGACTC	8850
rs563029243	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20064198	CTCCTTTTGAAAAAA[A/G]AACTTATTTTGTGTT	8850
rs563065382	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20117516	GTATGCTTTGAAATT[C/T]AGAAGGCCTATATAT	8850
rs563102153	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20153822	ACAAAGTTTTAAAAG[C/T]GTATTTAACTTGATG	8850
rs563107220	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20050172	ACCACTGCACTCTAG[C/T]CTGGGCAATGGAGTG	8850
rs563123520	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20088365	GCTGTACTAATTTAC[A/C]TTCCCACCAACAGTG	8850
rs563142891	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20072719	CAAATAAGATGAAAC[A/G]TGACAATCGAGCTAG	8850
rs563157436	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20052185	CAGAGAAGCCTTCCT[A/G]ACTCTCCGGTCTAAA	8850
rs563173949	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20124353	CTCAGCTTCTGGGGA[A/G]GCCTCAGGGAACTTA	8850
rs563203467	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20129352	TGGAGACCTTTTACA[G/T]TACATTCTTTGTTCT	8850
rs563210851	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20089256	ATTATTTTTTCTATT[C/T]CTGTGAAAAATGTCA	8850
rs563233768	snp	C/G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20123901	GCATCTGAGGGCATG[C/G/T]AAGGCAATGACATTT	8850
rs563239480	snp	A/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20123389	CTAATACAGGGTTGG[A/T]GAATTACAGCCTGCA	8850
rs563263512	in-del	-/AAAC	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20060602	AGAAACTCTGTCTAA[-/AAAC]AAACAAACAAACAAA	8850
rs563298331	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20126774	TTGTGGTGAGCCGAG[A/G]CCGTGCCATTGCACT	8850
rs563299323	snp	G/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20091754	TTCTCTGACCCATTG[G/T]TTGTTCAGGAGAATG	8850
rs563361479	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20104676	AACAAAGATGTGCCG[A/C]AAATGTTTGCAGTAT	8850
rs563405304	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20069967	CCTCTGAGATCTTTG[C/T]AACCTCTGAAGAGGT	8850
rs563425340	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20043200	TGGGCCACCATGCCT[G/T]GCTGAAAGTGTTCAT	8850
rs563433728	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20132001	AGATTTTTATGTGGA[C/T]TTATTGTGCTGAAAA	8850
rs563491075	in-del	-/AGG	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20103356	GTTTCATCAAGAAAA[-/AGG]AGAATTAATTGTGAA	8850
rs563497266	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20114424	GAGCTATATATGTGC[A/G]TGACAAATAAAAATA	8850
rs563526454	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20042178	CCAAGTGATGCTATG[C/G]TAGTCCACAGACCAC	8850
rs563544011	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20144568	TGCTGGGATTACAGG[C/T]GTGAGCCACCAAGCC	8850
rs563569079	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20046264	GGAGTTTCATGGGTA[C/G]AGGACTATAAAATTA	8850
rs563657200	snp	A/G	8.59247e-05	0.006554	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152549	CCCCTCTGCTTCTTA[A/G]AAACTCACCAAGCAG	8850
rs563661598	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20062579	CGATTCTCTTGCCTC[A/G]GCTTCCCGAGTAGCT	8850
rs563715201	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20079240	CACAGAGTCTGGCTC[C/T]GTCACCCAGGCTGGA	8850
rs563728700	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20108661	GCAATAGACTAGACC[A/G]TAGAGCAGGGGTCCC	8850
rs563762188	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20146137	GTGAATGTCACTAAA[A/T]AGACATGGTATAATA	8850
rs563797181	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20104053	ACTCAGTCACTGCCA[A/G]TGTGGAGCTTATTAA	8850
rs563908849	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20122323	TTTGGTGTCATATGG[A/C]CCATGTTCTCTGACC	8850
rs563910439	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20080554	TAATATATTTAGTTC[A/G]TTGTGCATAATTGTG	8850
rs563940559	snp	C/G			intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20135767	GGACTGGGAAAGTAC[C/G]GATGGGCATGTGTGA	8850
rs563975251	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20121613	TTGTAAAAGATAAAG[G/T]GTGTCATTTTATAAT	8850
rs563995164	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20115208	TATGATGTCTGTTTT[A/G]TACATCAAGTTACCA	8850
rs564036965	in-del	-/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20151987	AGATAGAGCCTCTTC[-/T]TGTATAATTCTGACT	8850
rs564106599	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20057615	TTTCTGATAAATTCT[C/G]TGTGTGTGTATTAAA	8850
rs564123887	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070007	ATTACAGAGAATTTC[A/G]AGGCCAGGTTCAGCC	8850
rs564136739	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20089387	TCTTATCACTTATTC[A/G]TGTCTTCTTCACTTT	8850
rs564151887	snp	A/G	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20058866	ATCTTTATCTCTTCA[A/G]ATCTTGGCTACTCAA	8850
rs564189020	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20064997	TGTGAGCTCTCCACC[A/C]CTTGTCTGTCTGTAA	8850
rs564191256	snp	A/G	0.000117812	0.00767413	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20111602	TTGTCACAGGTGGCT[A/G]TGTTACTGCAACGTG	8850
rs564214976	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20088525	CATTTTTCCATATAC[C/T]TGTTGGCCATTTGTA	8850
rs564219386	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20125110	GGCAGATCACGAGGT[C/T]AGGAGATCGAGACCA	8850
rs564219878	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20146461	CTTTTAAAAGCGAAA[C/T]TTTTTAGTAATGCCG	8850
rs564241660	snp	C/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20132074	ATTTTGGAATATCCT[C/G]TAATCTAAAAACAAT	8850
rs564244102	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20058286	AACATGGTGAAACCC[C/T]GTCTCTATTAAAAAT	8850
rs564337362	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20113572	GTAAAACTACCACCC[A/G]CTTCTCCTTTTAAAT	8850
rs564382526	snp	A/C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20086643	GTATTGGGGTGCACA[A/C/T]CCATGCATATTCCTC	8850
rs564397916	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20117563	AGAGCCTGGCACTTT[A/C]GTATATTCTGATTTT	8850
rs564413464	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20052375	CCATAAGGCCTCAGC[C/T]CATAGGAGAAACAGA	8850
rs564417082	snp	C/T	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20063365	GCTTTTGGTATTATA[C/T]CCAAGACACCATTGC	8850
rs564455847	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20146833	TTAGAAGCAGCCCAG[A/T]TCTGATGGCCGAACA	8850
rs564461085	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20102636	TTTTATTGCTTATTA[C/T]TTGCAGAATAACAGA	8850
rs564478076	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20075368	TTTTTTTTCTTCACT[C/T]ACCAAGCAATTCTCC	8850
rs564485061	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20062661	GAGACGGGGTTTCGC[C/T]TTGTTTGCCAGACTG	8850
rs564513382	snp	G/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20044204	TGTAGATCTAGGCCA[G/T]GCGCAGTGGCTCAGA	8850
rs564514494	snp	A/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152642	TTGTAAATGTAATAA[A/T]TAGCACTTTTGAAAA	8850
rs564644357	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20116722	ACATTTATTAAGTGC[G/T]CAGCTAAGATGCTTC	8850
rs564647988	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20044858	CATGCGGTTATTGAC[C/T]AAGCGAATGAACCAG	8850
rs564674508	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20145016	TGGCCAGGCTGGTCT[C/T]GAGCTCCTCACCTCA	8850
rs564695789	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20129649	CCCAAGTGCTGAGAT[C/T]ACAAACATGAGCAAC	8850
rs564699840	snp	A/C	0.00716266	0.059414	intron-variant	KAT2B	GRCh38.p7	3:20051222	AAAAAAAACCCAAAC[A/C]AAAAAAACAAATCAA	8850
rs564703590	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20116009	AGTACTAGTGAATGA[A/G]GAATTTTATTTGAAT	8850
rs564718901	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20074597	TTTTACTTCACACAG[C/T]AGATATATACTCTGT	8850
rs564791284	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20108794	CACCTCCTGTCAGAT[C/G]AGTGGTGGCATTAGA	8850
rs564792358	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20058283	GCCAACATGGTGAAA[A/C]CCCGTCTCTATTAAA	8850
rs564814483	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20045980	TCCTGAATCCACCCC[A/T]GCTCTGCCACTTGTG	8850
rs564853609	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20059788	TAAGTGTACAATTCA[A/G]TGATTTTTAAGAAAT	8850
rs564870872	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20080609	CATTGAATTCAATAA[A/T]GGTAAAATGAGGGCT	8850
rs564881425	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20087071	AGGCGTGAGCCACTG[C/T]GCCTGGCTGAGATTT	8850
rs564894534	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20049980	TGAGGCAGGCGGATC[A/G]CTTGAGCTCAGGAGT	8850
rs564896326	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20055714	ATAATTTTTACACAG[C/T]GATGTCAAGATCTTT	8850
rs564941019	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20150766	ATAATTCTTGCTTTG[C/T]TTCTGCTGCATTTTA	8850
rs564985828	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20123024	ACTTACTAATAATCT[C/G]ACAGTTGAAGGCATC	8850
rs564999991	snp	A/G	1.66076e-05	0.00288158	intron-variant	KAT2B	GRCh38.p7	3:20114876	TGCTATTACTCTTGT[A/G]TCTAGATTTCTGTCC	8850
rs565006409	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20081239	TAGCTGCCTGCCCAG[C/G]TGCTGCCTGTTCACA	8850
rs565027286	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20144761	AAATTAAGGCATGCT[A/G]TAAGTATAAAATCCT	8850
rs565031096	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20061631	TTCTCTACATCCTCT[C/T]CAACACTGTTTTCTG	8850
rs565059059	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20114236	TAATCACTGGTTCCA[A/G]TCCTGATCCTGCCAT	8850
rs565072794	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20100252	AAATGTGCTTTTTCT[C/T]GTTGTTGGTGCTTTA	8850
rs565095645	snp	C/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20067785	GTTCAAGCGATTCTC[C/G]TGCCTCAGCCTCCCA	8850
rs565132184	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20085692	TTTTTTGTGTTTTTA[A/G]TAGAGACAGGGTTTT	8850
rs565153650	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20072647	ACAAATGCTGCACTG[C/T]GTGCAGTGACTTTGT	8850
rs565159746	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20085043	CATAGCTTATCACAA[A/G]AAGAGATTAAAAGTT	8850
rs565171886	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20050274	AACAGTATCTCAACA[C/T]GATAAAAAGGAGTCA	8850
rs565197552	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20106418	TAATATCAATCAATT[C/T]ATTAAAACAACACCA	8850
rs565230353	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20056033	GTTTATCTGTTGACT[C/T]GTTATGGACATCTGG	8850
rs565240366	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20073232	ACTTTCCTGCCTTCA[A/G]TTATACAGTCTCCCC	8850
rs565266741	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20140833	TCTGTTTCCTTTCTC[A/G]GTTACCATTTCTACA	8850
rs565302751	snp	A/T	0	0	intron-variant	KAT2B	GRCh38.p7	3:20123112	GTAATAAAAATCCAT[A/T]GACTCTTTACTGAGA	8850
rs565313775	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20121618	AAAGATAAAGTGTGT[C/T]ATTTTATAATAGAAA	8850
rs565340926	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20119029	TTTCCATTGCATCAG[A/G]AGGCATATGATGTTG	8850
rs565358861	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20060979	AACAAAACTGTGGTA[A/C]AATATAGATGATCTA	8850
rs565377105	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20068661	GAGAGCAGAATCTTT[A/G]TTTCATAGTCAATAG	8850
rs565433262	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20135347	GCATTGTTATATTAG[A/C]AAAAACTCCGAAAAA	8850
rs565436729	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20120981	TCAGCCTCAGACTTT[C/T]TAAAAAAAATCATAA	8850
rs565451861	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20049149	ACAGGTGTGAGCCAC[C/T]GCGCCTGGCCGGGCA	8850
rs565472923	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20079180	TGCTGGGATTACAGG[C/T]ATGAGCCACCACACC	8850
rs565481167	in-del	-/A/AA			intron-variant	KAT2B	GRCh38.p7	3:20105801	CACGACCCTGTCTGA[-/A/AA]AAAAAAAAAAAAAAA	8850
rs565489679	snp	A/C	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20129260	AATCCAGTGAGATTA[A/C]TTTTGGAAATTTATT	8850
rs565509875	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20054363	TGAATTCCTGACCTC[A/G]TGATCCACCCTCATC	8850
rs565564809	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20095056	TTGGGTGGGGAGGCT[A/G]AGGCTCAAGAACATG	8850
rs565593737	snp	A/G/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20135975	AAGGAATTGGCCTAC[A/G/T]TTGGCGGTGTTCTAG	8850
rs565627154	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20108977	TCATGAAAGCAATCC[C/G]TGGTGCCAAAAAAGT	8850
rs565673955	snp	A/C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20068621	TGTTTTCCCCATCCC[A/C/T]GGCTACCCCTAATGT	8850
rs565674627	snp	A/G	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20122059	TAACATGACTACAAG[A/G]AGAAATAATCAAATC	8850
rs565677484	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20105019	GCCTCCCAAGTAGCT[A/G]GGATTACAAGTGCGT	8850
rs565691582	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20074217	TTCTGGCCTTACTTA[C/T]GATAGTAAAAAGCAT	8850
rs565710611	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20137155	AGTGTTTTCTACTTA[C/T]AAGAACAGGCATTTG	8850
rs565712689	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20087080	CCACTGCGCCTGGCT[A/G]AGATTTTTTAAAGGA	8850
rs565768028	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20108181	AAAACTAAATGGAGT[C/G]CTACTAGAACAATCA	8850
rs565773042	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20100921	ATCTAAGAACTGCAT[C/T]ATATGTGGGCTACTC	8850
rs565834161	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20149108	GGTGCTGTGCCCACA[C/T]CACTCTAAAATTAAT	8850
rs565886602	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20061093	CATCCACAGAACACT[C/T]TTCAGCTTGCAAAAC	8850
rs565886979	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20060682	GTAATCTTAGTACTT[G/T]GGGAGGCTGAGGTGG	8850
rs565907766	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20086626	CACCCCACAAAAATG[C/G]TGTATTGGGGTGCAC	8850
rs565921359	snp	A/C	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20143161	CAGTAGATCATAGGA[A/C]TGAGCTGTGGACTTC	8850
rs565923626	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20072723	TAAGATGAAACATGA[C/G]AATCGAGCTAGTTAG	8850
rs565934357	snp	A/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20079300	ACTTCTGCCTCCCAG[A/G]TTCAAGCTATTCTCC	8850
rs565944884	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20072167	AAGCACTCAAATCAA[A/T]TACCACCTTTGGGTT	8850
rs565954251	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20067301	CAAGTGGTTTCAACA[C/T]GTGCGGTTAATATTC	8850
rs566020643	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20084665	AGGGAAATGAGCCTC[C/T]TCAGGTTTCACTTAA	8850
rs566055058	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20092775	GGTGTGATGTCGGCT[C/T]ACTGCAATCTCCGCC	8850
rs566062804	in-del	-/T			intron-variant	KAT2B	GRCh38.p7	3:20061022	TGAACTATTTTTAAG[-/T]GTCTAGTTCATTGGT	8850
rs566064698	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20151044	TTAAATGAGAGAACA[C/T]TTTGATCTGTTCAGT	8850
rs566080496	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20060574	CCATTGCACTCCAGC[C/G]TGGGCAACAAGAGAG	8850
rs566101763	snp	G/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20150349	ACGATTTCCTTATTT[G/T]ATTTTTCTAATAACA	8850
rs566217982	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20055781	GAACTTTTCCATCCC[C/T]CTAGAAAATTTCTGC	8850
rs566219969	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20146646	TAGATGCCCCCTTGT[A/T]ATAGCTGTTAATATC	8850
rs566256728	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20124728	GAATGCACAAGAAAA[C/T]TGTTAAATTTTCAGG	8850
rs566280688	snp	C/T	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20059621	GAGGCAGGAGAATGG[C/T]GTGAACCTGGGAGGT	8850
rs566334782	snp	C/T	0.00478085	0.0486577	intron-variant	KAT2B	GRCh38.p7	3:20095596	GAACACATCATTCTC[C/T]TTGAGGCTTTTACAC	8850
rs566346491	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20059290	TGGTGGCATGCGTCT[A/G]GTAGTCCCAGCTACT	8850
rs566351603	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20075481	GGTTAAGGGCACAGT[C/T]CCACAATAGTGCTCC	8850
rs566367555	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20113834	CCACTTGGCTTTAAT[A/G]TGTGCCTCTTTCCCC	8850
rs566404807	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20054402	AAAGTGCTGGGATTG[A/G]TTACAGATGTGAAGG	8850
rs566421672	snp	A/C	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20120466	CTCCTGACCTCAGGT[A/C]ATCTACCTGTCTCGG	8850
rs566432580	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20048813	CTACTCACACATGGG[A/G]AGAGAAGGAGGGGAA	8850
rs566436024	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20042779	AGCATATGTGGCCTG[A/C]ATTGATATTTTTGAT	8850
rs566472075	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20054050	TGATCCATCCTCCTC[A/G]GCCTCCCAAAGTGCT	8850
rs566472973	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20142189	GCCAGAAGCGCAGAG[C/T]TATTTTAGATGGCTA	8850
rs566487782	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20130953	GTTCTAATGGTAAGA[A/T]CCAATCTTTAGTAGA	8850
rs566503068	snp	A/G	0.00438332	0.0466095	intron-variant	KAT2B	GRCh38.p7	3:20092069	AATGGAATGTTCTGT[A/G]TATGTCTGTTAGGTC	8850
rs566547353	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20134400	TGTTTTGTTGTTTTT[A/G]TTGTTGTTGTTGTTT	8850
rs566602498	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20091343	TCTGTGGTATCAGTT[A/G]TAATGTCTCCTTTTT	8850
rs566611209	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20127611	TCTCACTAAGGCCTG[C/T]AGAGCTTGGGAAGAT	8850
rs566691972	in-del	-/GT			intron-variant	KAT2B	GRCh38.p7	3:20142890	TCTATGTGCCTGTGT[-/GT]GTGTGTGTGTGTGTA	8850
rs566700155	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20141548	TCTGTTATTCGTTTA[A/G]TGCACTTTTCTCTAA	8850
rs566705156	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20044331	ACAAAAAATAAAAAA[G/T]TAACCAGGCGTGGTG	8850
rs566720256	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20118427	AAAAAGAGAAAGAGA[A/G]CTATATAGGCCAGGC	8850
rs566731330	snp	C/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20139964	ACTTAACACCTGTTT[C/G]TGTTTTAAACTTTTT	8850
rs566787396	snp	A/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20097705	CCATGCCCGGCTAAT[A/T]TTTGTATTTTTAGTA	8850
rs566802973	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20125528	TTCTTTAACATATTG[C/T]CTGTGGATGCTTTTG	8850
rs566808165	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20149690	TAAAGTGAACACACA[C/T]CTATATGCTTTTCTT	8850
rs566813476	snp	G/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20040109	GGCACGCACACCTAG[G/T]CCGCAGTCCCGAGGA	8850
rs566858186	snp	A/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20133281	ATTGTATGCATTGCA[A/T]TACTGGAAAAAAACT	8850
rs566880667	snp	G/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20064705	AATAATGGCAATAAT[G/T]CATACTTTACTTACA	8850
rs566892095	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20042934	AGACAGGGTCTCACT[C/G]TGCCACGTAGGCTGG	8850
rs566915517	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20046782	GTCTTTTTCATTTGT[C/T]AGCATTTAGAGCAGT	8850
rs566948984	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20112044	CATTGTCTCTGACTC[A/G]CATAGAATGGGGCAG	8850
rs566976977	snp	C/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20111279	GGAAAGGCTAAATAG[C/G]GTAATCAAATTTTCA	8850
rs566981102	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	KAT2B	GRCh38.p7	3:20071385	CTGACTTGAAGCAGT[A/G]AATAAATGGTGAGAG	8850
rs566992318	snp	A/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20072843	TTAATGATAATAATG[A/T]TCATTTTTATTATTT	8850
rs567007581	in-del	-/A	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20071184	TTGCGCTAGTCTTCT[-/A]AAATCTGTATATTTT	8850
rs567025414	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20140683	TTTTAGTGGAGACAG[A/C]GTTTCACCATGTTGG	8850
rs567041616	in-del	-/TTTC			intron-variant	KAT2B	GRCh38.p7	3:20067986	TAATTTCATTTCTTT[-/TTTC]TTTCTTTCTTTCTTT	8850
rs567041710	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20090585	ATCTGCTGTTGAATT[C/G]AGATTGCTGGTTTTC	8850
rs567055572	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20100484	AAGAGTTTTTCTGTT[A/G]GGTGTTGTCAGTATC	8850
rs567056773	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20082822	TGCAATGAGTATGGC[A/C]GACTAAAGGTAGTAC	8850
rs567144664	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20145659	AACAAACAAAACATC[A/T]CTCAAAATTTCTCAG	8850
rs567169512	snp	A/G/T			intron-variant	KAT2B	GRCh38.p7	3:20042200	ACAGACCACATTCCA[A/G/T]TTCAGACCTGGACAA	8850
rs567205894	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20049236	ACCTCATTGACTTAT[C/T]GTGAAGATTAAATAC	8850
rs567233590	snp	C/T	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20079422	TTGACCAAGCTGGTC[C/T]CAAACTCCTGACCTC	8850
rs567264662	snp	G/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20090827	GCAACCTCAATCTTG[G/T]GGGGTGGGTTCAAGC	8850
rs567285803	snp	G/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20120234	TTTTTTCCTTTTCTT[G/T]TCTTTTTATTTGAGA	8850
rs567297042	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20085879	TTGATTATTCTTTTT[C/T]TATTTGATAATGTAA	8850
rs567330023	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20058914	GGAACTTTTAGAAAT[G/T]TAGAATCTCAGGTTC	8850
rs567369221	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20121941	TAAGACTCATTTGGG[A/G]TTGGTTTATTACATA	8850
rs567369235	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20113937	AAAATTTGGTTCAGG[A/G]AAAAAATGAAGAAGA	8850
rs567476911	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20060077	CTTCTTTATCTTTCA[C/T]TGCAAGTAATAATCC	8850
rs567493597	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20125599	TGGCTCACAACGTCT[A/G]AAATATTTTCTATCT	8850
rs567540792	snp	G/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20135440	CGGGCAGATCACAAG[G/T]TCAGGAGATCGAGAC	8850
rs567548221	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20065676	GTCCCATGGAGCATG[C/T]ACACATGCAAGAACC	8850
rs567589885	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20112309	ATAGAGAGCTCCTTC[A/G]GCGTGATGAACCTCT	8850
rs567619043	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20119535	TCCCATGTGCACTTC[A/G]TTTCTTGTTACCTAA	8850
rs567631565	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20126676	AAAAATACAAAATTA[A/G]CCAGGCCTGGTGACA	8850
rs567662238	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20072088	TAGCAAAGTGTGTGG[C/G]TCAGCTGCGTGAGCT	8850
rs567722134	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20056277	GGACTTAATTTGTTA[C/T]AAGGGAGGTGGTGAT	8850
rs567728419	snp	C/T	0.00199481	0.0315187	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20040541	GGGGCAGGGGCCGGG[C/T]CCGGGGCGCTGCCCC	8850
rs567747290	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20096247	ACTGACACCAGTCAC[C/T]GATTACTGCTGCCAT	8850
rs567797857	snp	A/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20133831	TGCACGCCGTCAAGT[A/G]CAATATTTCATTTTA	8850
rs567828060	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20084462	TCTTTCTTCTCTTCT[A/G]GGAAACTGTTGCTGC	8850
rs567843548	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20077161	AAGTAGAAAGAACAT[G/T]CAGTTGGGAACTAGG	8850
rs567911070	snp	A/G	0	0	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070082	CCTAGACAAAAGACG[A/G]TCACTTGAGCTACTC	8850
rs567915903	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20078043	AGCTGGTGTGGTGGC[A/G]TGTGCCTTTTAGTCC	8850
rs567923559	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20076108	AAACTCAGGTATGAT[C/T]GAAAGGGGCTCATGA	8850
rs567965605	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20144379	CTGCAAGCTCTGCCT[C/T]CTGGGTTCGCACCAT	8850
rs567988002	snp	A/G	0.0107246	0.0724382	intron-variant	KAT2B	GRCh38.p7	3:20058477	AAAAAAAAAAAAAAG[A/G]TTTTCAGAGATGCTT	8850
rs567990709	in-del	-/T/TT	0.555591	0.165669	intron-variant	KAT2B	GRCh38.p7	3:20139059	CACCATGCCCAGCAA[-/T/TT]TTTTTTTTTTTTAAT	8850
rs567993727	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20095010	AAATATACATTATTT[A/G]CATACATTAGCCACC	8850
rs568002321	in-del	-/AGTGC	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20129424	TGTTGCCCAGGCTGG[-/AGTGC]AGTGCAGTGGTGTGA	8850
rs568006892	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20103462	TATCCTGGGCTGGAG[C/T]GCAGTGGCATGATCA	8850
rs568009486	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20059024	CACTACTCCTAATTA[C/T]ATCAGCATAATTCAA	8850
rs568018131	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20052798	CATGGTGAAACCCCA[C/T]GTCTACTAAAAAAAC	8850
rs568064130	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20147560	ACTTTCTTGCATTAC[A/C]AGCAGGGCCTTAGCC	8850
rs568069932	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20064389	GCTATTTTGTAATAT[A/G]CAATATATTATTGTT	8850
rs568087586	snp	A/G	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20140753	TGCCTCGGCCTCCCA[A/G]ATTGTTGGGATTACA	8850
rs568100787	snp	C/G			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20069859	CTGCATTTTAATAAC[C/G]CTTAGGCCAAAGTTG	8850
rs568136798	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20141348	AGTTGAATACATAAT[A/G]ATTTCAAATTTTCTA	8850
rs568145613	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20047409	ATATGACTAACACTT[A/G]AAATCTGAAAAATCT	8850
rs568206466	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20053103	GTGTGTTTCCCCTTG[A/G]TTCATGGCAGACTTG	8850
rs568266976	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20110415	GTAGCTCATGCCTGT[A/C]ATCACAGCACTTTGG	8850
rs568327185	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20084616	AAAAAAAAATCACAA[A/C]ACCACAAGCACATTT	8850
rs568329152	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20106610	ATAAAATGACTTTGA[A/G]GAAATGAATGAAAGC	8850
rs568340411	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20082135	CACCTCCTGGGTTCA[A/G]ATGATTCTCATGCCT	8850
rs568374512	snp	G/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20139091	ATTTGTAGAGATGGT[G/T]AGGGGTTGGGAGAGA	8850
rs568393403	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20051928	ATTCATTTAACATTA[A/T]ATTCCATGGGCTGCT	8850
rs568403092	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20153986	TTCAGAATGCTCACA[C/T]TGAAAATGCCTCAAC	8850
rs568417268	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20080376	CCTTTCCTTCATTTT[C/T]TGCCAGGGAATTCTG	8850
rs568467297	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038662	AAATCCATGTTAGAG[G/T]TTGATCAGAGAAGCA	8850
rs568480845	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20129593	GTTGGCCAGGCTGGT[C/G]CTGAACTCCTGACCT	8850
rs568488694	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20043646	TGCCTAGGGCCACCG[A/G]CTGGGGTGCGTGGCC	8850
rs568519002	snp	A/C	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20117177	CTGTCATAGTACAGG[A/C]TGGAGAAGGAAGAGG	8850
rs568534180	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039234	TGTATGCTCCACAGT[A/C]ATCAACAGTGAAAAC	8850
rs568534735	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20059559	AAATACAAAAAATTA[A/G]CCAGGTGTGGTGGCG	8850
rs568542093	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20124679	ATTTTGGATATATTA[A/G]TATTTAGTAGTGTAC	8850
rs568578552	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20132117	TGGTGGCTCACACCT[A/G]TAATCCCAGCACTTT	8850
rs568581729	snp	A/T	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20084590	TAAATAAATAAATAA[A/T]TAATAAATGCAAAAA	8850
rs568603162	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20145268	TGCGGCTAGTAGAAA[A/G]ATTTAAATTACATGC	8850
rs568647642	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20061291	TTCATTCAGGTTGTG[A/G]CATGTGTCAGAGTTG	8850
rs568659183	snp	A/C/G	1.64895e-05	0.00287132	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20148279	CCAGCTTTACAGCAC[A/C/G]CTCAAGAGCATCCTC	8850
rs568665407	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20064633	TGTGCATCTGCAGGG[G/T]AGAATGAGTAACCCC	8850
rs568701571	snp	A/C	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20101668	TGAGGGATGTAAATC[A/C]TCTATACCCAGTGTG	8850
rs568720323	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20045144	CTTAGCCTCCTGAGT[A/G]GCTGAGACCACAGGC	8850
rs568721863	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20095477	TCTCCATATGCCAGG[C/T]CGTGGCTGTGAAGGC	8850
rs568758160	snp	G/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20130852	ATAGAATGGATGAGT[G/T]TAGTGTGTGTGTGTG	8850
rs568760861	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20138329	TGGTTCATACTGTGT[A/G]TATAATAATTTTGGT	8850
rs568782840	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20102213	CCTGGCTACTTGGGA[A/G]GCTGAGGCAGGAGAA	8850
rs568795604	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20053976	CTAATTTTTGTATTT[G/T]TAGTAGAGATGGGGT	8850
rs568835384	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20047484	GTATAATTTATAGAT[C/T]ATAAAACTTGCCCAC	8850
rs568837572	snp	A/G	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20141491	CTCCCAGTTGGGTGG[A/G]GTTTGCAGCTGTGTC	8850
rs568838732	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20148775	TGAAAGCTGGCACTT[C/T]AGATATAACTTTGCT	8850
rs568840988	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20126834	TTCAAAAAAAAAAAA[A/C]AAAAAACCCACGAAA	8850
rs569003940	snp	A/G	0.00517822	0.0506191	intron-variant	KAT2B	GRCh38.p7	3:20133975	ATTGATTCTATAGAA[A/G]ATATTTATGTATTTT	8850
rs569076920	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20104165	AAACAGCAAAAGAGT[C/G]CTTTATAGCCCAGCC	8850
rs569077645	snp	A/G	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20147102	TGAATATCATTGGCA[A/G]TTTTGTTCAGTTCAA	8850
rs569084952	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20053551	AAAAACAAGACAAAA[C/G]AAAAAAACTCAGGAA	8850
rs569095251	snp	C/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20104805	CCATAAAAATTAAAA[C/G]CAGACTGAACAGTAG	8850
rs569097753	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20059119	GTTTTTTAAAAATAT[A/T]ATTAAAATATCTTGC	8850
rs569114441	snp	C/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20146537	CTTTATTGCCCTGCC[C/G]GTCTCTGTGTTATCT	8850
rs569128460	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20124808	CATGGCACCTGGTTA[C/T]CTGGATAGCCAGTTC	8850
rs569150707	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20076157	CCTCCTGCTCAGGAA[A/G]TCCCAAGGGTTTTAA	8850
rs569187790	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20075503	TAGTGCTCCCACTTC[A/G]GATGCCAATTGCAAG	8850
rs569195516	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038723	GAGAATGGCAAAAAT[A/C]TGCGAAACATCTCAG	8850
rs569220495	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20148165	TTCAGGTTTTTGTAA[C/G]AATGAGCTGAATAGT	8850
rs569227711	snp	C/T			intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20136606	AATCTACATTCATTC[C/T]GAAAACTTTTATATT	8850
rs569349306	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20116901	ATTCCTAAATATTAC[A/G]CTGTATTAAGAGAGC	8850
rs569390987	snp	A/G	0.0271762	0.113356	intron-variant	KAT2B	GRCh38.p7	3:20122083	TCAAATCAACCAACG[A/G]TTGAGGCTTTAAACA	8850
rs569394376	snp	C/T			utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20154272	TTTTCTTATAGATAT[C/T]GTGCAATAAAGCTGA	8850
rs569418537	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20049085	CAAGATGGTCTCGAT[C/T]TCTTGACCTCGTGAT	8850
rs569419034	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20130922	TGTGTGTGTGCATGC[A/G]TGCGTGTGTGTGTGT	8850
rs569457836	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20096110	GCCCAGCGAGCAGAG[G/T]GTTGGGTGGGAGGAG	8850
rs569478900	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20134724	CACCGCGCCCAGCCC[A/T]CTATTGAAGATACAA	8850
rs569540072	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20124369	GCCTCAGGGAACTTA[C/T]ACTCATGGTGCAGGG	8850
rs569540763	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20089561	GTGCGCCACCATGCC[C/T]GGCTAATTTTTTTTA	8850
rs569552595	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20102812	GCACATCAAGCTTGC[A/T]TTAGGGAGCTTTAGT	8850
rs569557386	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20087606	CACACAATTGATCTC[C/T]AGAACTTCTGTGTAA	8850
rs569573280	in-del	-/CTTA	0.00676609	0.0577691	intron-variant	KAT2B	GRCh38.p7	3:20147244	TGCCCTCTGGCAGAT[-/CTTA]CTTTTATGCTAAATC	8850
rs569582644	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20052454	ATCTCGGGTGGATCA[C/T]ACCTTGCACATAGTA	8850
rs569607716	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20102275	GAACTGAGATCGTGC[A/G]CTCTGGGCAACAGAG	8850
rs569613394	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20116207	TAGCATTTAGTGGAC[A/G]TGTTTTCTGTGGTTA	8850
rs569623077	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20101014	GACCTTTTCAGTCCA[C/T]GGTTTTGATTTTCTC	8850
rs569625427	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20123157	TTATGCCACATTTGC[C/T]ACCTCTCTTTCTCTC	8850
rs569675313	snp	C/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20109548	GTCTTGAACTCCTGG[C/G]CTCAAGCGATCTTCC	8850
rs569676611	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20068707	AGGCCTCAATAAATA[C/T]TGTTGAAAGAATGAG	8850
rs569690791	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20122084	CAAATCAACCAACGG[C/T]TGAGGCTTTAAACAA	8850
rs569751312	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20101816	GTAGAAATGATAGTA[C/T]ATTGGATACATTGGA	8850
rs569752192	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20119534	GTCCCATGTGCACTT[C/T]GTTTCTTGTTACCTA	8850
rs569762211	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20149586	CTCCTTGAAAACTGA[C/G]TTATTTACAGGTGTT	8850
rs569765719	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20057053	AAGAGGGGAGGAAGT[A/G]TTTCTTCTAGTTGGC	8850
rs569826735	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20074262	ATTCCAATGTAGGAG[A/G]TGATTGTGAAGAAAT	8850
rs569839251	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20080916	TTTGTCTTTTTAAAC[A/G]CAGCTACTGGAATAC	8850
rs569908406	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20056202	GGTGTCTTGGGCTAG[A/G]GTAGCAGGAATGGAG	8850
rs569936536	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20109872	AAAAGTTGAGAGAAG[A/C]CATAGAAATAGTAGC	8850
rs569956713	snp	A/G	0.00478085	0.0486577	intron-variant	KAT2B	GRCh38.p7	3:20092696	TTTGGTCTCTGTATC[A/G]TTTTTTGTTGTTGTT	8850
rs569970104	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20061783	TATATAATTTATAAT[A/G]CATAAAATATATTAT	8850
rs569997486	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20100689	TAAGAATTCATTGCT[C/T]TTTTATTTGAAATTA	8850
rs570001220	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20148935	ACTTGACTGCTGTAC[G/T]TTCAGAGGGAGAAAT	8850
rs570027982	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20049934	GCTGGGCACCGTGGC[G/T]CCCCCTTGTAATCCC	8850
rs570042449	snp	G/T	0.00676609	0.0577691	intron-variant	KAT2B	GRCh38.p7	3:20138204	AATGCTTTGATTTTT[G/T]TATTTTAAAATTTTT	8850
rs570051622	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20055859	CTGATTTGTGTCACT[G/T]TAAGTTAATTTAGCT	8850
rs570064889	in-del	-/T			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038524	TGCTTGTGATTTTTC[-/T]TTTTTTTAAAAATTT	8850
rs570070130	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20151413	TTTATAACATACTTA[C/T]AATTTGGGATATTGG	8850
rs570115302	in-del	-/CAA			intron-variant	KAT2B	GRCh38.p7	3:20060966	CAACAACAACAACAA[-/CAA]AACTGTGGTAAAATA	8850
rs570120370	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20130072	AACCTCCGCCTCCTG[C/G]GTTCAAGTGATTCTT	8850
rs570128576	snp	A/C/T	0.00239393	0.0345281	intron-variant	KAT2B	GRCh38.p7	3:20087138	TGAGTTCTAGTGTTC[A/C/T]ATGCCACTGTAAGAT	8850
rs570142571	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20110402	TTGTCTCAGTTTGGT[A/G]GCTCATGCCTGTAAT	8850
rs570158923	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20119318	TACCATAACTCCGTC[C/G]TTATTTCTTTGTTGG	8850
rs570160566	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20137386	TGTGAATGAGAAAAA[C/T]AGATTCAGTTTCTGG	8850
rs570264235	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20097147	TCTTTGGAAAAAGAT[C/T]TTAGTTGAAGAAAAA	8850
rs570323991	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20082036	TACAGTTCCTAATAA[A/T]AAGGTTTTCTTTTTT	8850
rs570327957	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20075699	TGCACATTGCAAGGT[C/T]TGGGGAAGGGGAGTG	8850
rs570332071	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20098368	TTAAAACTTTGCTCT[A/G]TCACTTACTAAATGT	8850
rs570405125	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20109582	TTGGGCCTTCCAAAG[C/T]ACTGGGATGACTGGT	8850
rs570406228	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20151097	TGTGAGATTTGATGA[C/G]TCTTTGTGTTTCTTA	8850
rs570412436	snp	A/G	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20058055	GTTGTTTTGTCTTGG[A/G]TCATTTCCTCATGAT	8850
rs570414325	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20063999	CTATTGAATGGTCTT[C/G]GCACACTTGTCAAAA	8850
rs570448797	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20153849	GATGTTTTCTATCAG[A/C]ATAAATAAAATGGTC	8850
rs570450290	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20153152	AAATAATGCAAACTT[C/T]TAAAATAAGCATCTA	8850
rs570475454	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20063521	CACCTCACAGCAACT[C/T]CTGAGTAGGCCTCTT	8850
rs570586428	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20081387	GCAAGGTTGACAGCT[A/G]CACCGTGATTCTTGG	8850
rs570616164	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20068780	CTCAAGGTGTTTTTG[A/G]TTATTACTGTTTTTT	8850
rs570626484	snp	A/C/G			intron-variant	KAT2B	GRCh38.p7	3:20109048	TAGGTTCTACCATCT[A/C/G]GGTTTGTGTAGGTAC	8850
rs570628851	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20074992	ACCATAAGGCCGGGC[A/G]TGGTGGCTCACGCCT	8850
rs570686043	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038559	GGCAACATTTATATC[C/T]AGTGAAATGTACAGA	8850
rs570687440	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20063798	CAACTGCTTCGGCCT[C/T]CCCAAGTGCTGGGAT	8850
rs570687537	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20084148	TTTAGACAACTACGT[A/G]TTTATATAGTGTAGT	8850
rs570755915	in-del	-/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20074761	GCTGCCACTGAATCA[-/T]TTTAGGATTCAACTC	8850
rs570790826	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20056921	ACATAACATGATTTG[A/G]ACTGCAATTGCCTTG	8850
rs570852460	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20056320	ATGAAGGATAATGTC[C/T]AGGTTTTTGGCCTGA	8850
rs570867059	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20137523	TTGCAGTTCCTTCCT[G/T]TCTCCGTTCCTCCCT	8850
rs570869910	in-del	-/TTCTC			intron-variant	KAT2B	GRCh38.p7	3:20141556	TCGTTTAGTGCACTT[-/TTCTC]TAACAAATAGCTTAG	8850
rs570905414	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20123164	ACATTTGCTACCTCT[C/G]TTTCTCTCTGCGCCT	8850
rs570938636	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20131278	CTTCGGCCTCCCAAA[A/G]TGCTGGGATTACAGT	8850
rs571008139	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20151528	CAGACTTCAAGACAA[C/T]CAGGGAACCATAAAT	8850
rs571013242	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20044004	TTAAACTTCACAAAC[C/G]AAACCAAAAAAGAAG	8850
rs571044140	snp	A/G			missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20119712	CCTCTTCTGGACTTG[A/G]GGCAAACCCAGGTAA	8850
rs571100912	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20152025	TAACAGTAGTCAGTT[C/T]ATCATACTTATTGTT	8850
rs571102200	snp	A/G	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20050773	CAGTGGCATGATCTC[A/G]GCTCACTGCAGGATC	8850
rs571115714	snp	A/G	0	0	intron-variant	KAT2B	GRCh38.p7	3:20142925	CATATACCTATGTAC[A/G]TGTATGTGTGGATAG	8850
rs571169228	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20144506	GTGTTAGCCAGGATG[G/T]TCTCGATCTCCTGAC	8850
rs571198093	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20043415	AATTACAGAGAAGTT[C/G]AGAAAAACTACTTTC	8850
rs571210681	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20042974	GCATGATCGTAGCTC[A/G]CTGCAGACTCAACCT	8850
rs571272534	snp	C/G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20080010	CCTTCAAGTTCCTGC[C/G/T]TCTAGCACTGGCTGA	8850
rs571283425	snp	C/T	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20074140	AATCCATGCCAGAAA[C/T]TTAATCTGTGTGTAA	8850
rs571284583	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20042496	ATCTCACAAATCACC[A/G]TTAAAGAACTTATGT	8850
rs571309551	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20054532	CTTGTCAGTAACCTC[A/C]GGGCAAGTTGTATGG	8850
rs571339163	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20113722	GTGAGAGCTGGGACC[A/G]GCTTCCCAGCACCCA	8850
rs571340306	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20093154	GAAACAGACTCTGAG[A/G]CAAGGATTTGAGTGC	8850
rs571341151	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20105639	ATAAAAAACTAGCTG[A/G]GTGTGGTGGCATGTG	8850
rs571360929	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20115367	AGGAAGGAAGACAGA[C/T]GCCTTCTGGAGTCGC	8850
rs571369149	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20114584	TGGAGGGCTGAAATC[A/G]TGCTCTGAGATTCAC	8850
rs571451429	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20086050	CCACAGTGGATGGAT[C/T]GCTTGAGCTCAGAAG	8850
rs571454174	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20049811	CTGTGCTGGCCCAAT[A/T]GAATTCTCTGTTGAA	8850
rs571468347	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20092735	TGAGATGGAGTCTCC[C/T]TCTGTCACTAGGCTG	8850
rs571477753	snp	C/T	0.000399281	0.0141238	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20119652	ATTCAACCTCATCTT[C/T]CCTTGAGCAGCCAAA	8850
rs571495040	snp	A/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20128351	TTTCTTATGACCTTG[A/T]CCCTAAGGGAAAACA	8850
rs571500589	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20129002	ATGAGAGCGAAACTC[C/T]ATCTCAAAAAAAAAA	8850
rs571516126	snp	A/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20085185	TGAGACTCCATCTCT[A/G]TGTCTATTAATTTAA	8850
rs571538766	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20086538	CTCAGGAGGTCAAGG[C/T]TGCAGTGAGCCAAGA	8850
rs571613864	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20114559	TAATGACAGTGACAG[G/T]GCAGCTATATGGAGG	8850
rs571624767	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20060219	TCTTAGTATGGATAT[A/G]TTTCTGTTTCTCTTG	8850
rs571624819	snp	A/G	0.00517822	0.0506191	intron-variant	KAT2B	GRCh38.p7	3:20066741	TATTTAACCCACTGC[A/G]CCGCATTAAAAAAAA	8850
rs571675327	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20099336	CTGTGCCCTAGATGA[C/T]GCGTATGCCGTGCAG	8850
rs571692727	snp	C/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20054587	CATCCTAATCAGTCC[C/G]CATGCGTTGTGTACT	8850
rs571693479	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20055020	AAGTCAATGCAGAGA[G/T]AAACCATTGTGAGCC	8850
rs571756799	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20078127	GAGGTTTCAGTGGGC[C/T]GAGATCGCACCACTT	8850
rs571778157	snp	A/C/T			intron-variant	KAT2B	GRCh38.p7	3:20042672	TATTTATTGGGTTCT[A/C/T]ATCACCAGCACCTCT	8850
rs571792572	in-del	-/GA			intron-variant	KAT2B	GRCh38.p7	3:20096972	AGAGAGAGAGAGAGA[-/GA]AAGAGAGTGGGGGAA	8850
rs571810514	snp	C/T	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20060557	AGTGAGCTGAGATCA[C/T]GCCATTGCACTCCAG	8850
rs571841332	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20042085	GCATGGGAATCTCCT[C/G]GGGAAGCTGGTTAAA	8850
rs571860888	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20121433	AACCAAACATGAGAA[C/T]AGAAAGGAGAAAAAA	8850
rs571893758	snp	A/G			intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20137225	TTAGAGAGTGTCACT[A/G]GCACATAGTAAGTAT	8850
rs571911634	snp	A/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20107343	GCCAATAATATATAT[A/G]TTTTTTACCCAATAT	8850
rs571937688	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20072108	CTGCGTGAGCTGTAG[C/T]ATGCAGATTCCAGCC	8850
rs572019301	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20060732	GAGTTTGAGACCAGC[C/G]TGAGTAACATAGTAA	8850
rs572071980	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20135143	ATTTGTGTTTTTATC[A/C]AAGTTTTATTCAAAC	8850
rs572106449	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20050250	CAGTTTATATAAGAC[A/G]GTTCACACAACAGTA	8850
rs572142689	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070112	CACTGGGGGATGTAG[C/T]TATGGGGATGCTGAT	8850
rs572145747	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20143936	CCTGTCAGGTACTGT[A/G]CTCACTACTTGGGCA	8850
rs572155590	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20065946	CTAGTAGTCCTGTGT[A/G]TTAGTTTCTTAGGCC	8850
rs572162208	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20099637	ATAACTCTGGCCGTG[A/G]ACATGAAGGCCAATT	8850
rs572175858	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20100198	GTTTGGGGAAGAAAA[A/C]CATTAAGTAGAACAT	8850
rs572225479	snp	C/G	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20078943	GCAGTGGCGCGATCT[C/G]CACGATCTCAGCTCA	8850
rs572229020	snp	G/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20122518	TCACAATGGCTCTCT[G/T]TCCTGTCTTCCTTTG	8850
rs572231072	in-del	-/AAG	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20051206	TCTGTCTCAAAAAAA[-/AAG]AAAAAAAACCCAAAC	8850
rs572252583	snp	A/T	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20142451	TTGTTCCAACTGTGA[A/T]AAACCCCTCAAGGAA	8850
rs572255487	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20127934	GAGGCAGAGCTCAGG[C/T]GGTAATGCTCACTTG	8850
rs572269728	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20105329	TCCATGAAGAAATAA[C/G]CTAAAAAGAAAGTGT	8850
rs572281284	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20080872	TAGGTTAAATAAAAT[A/G]TATTATTTAATGAAT	8850
rs572309471	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20079598	AAGAAAATACCAGTA[G/T]TTTTCTCATGGATAT	8850
rs572341750	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20146280	TGTATCCATAGACTT[C/T]TTTCCCTAAACACAT	8850
rs572344790	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20114121	TTTTAAATCACCTGC[C/T]CTATTCTGATAAGCA	8850
rs572348495	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20106589	GAAAAGTATAAATTG[A/T]GGTCTATAAAATGAC	8850
rs572364057	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20049023	CCCGCCACCACGCCC[A/G]GCTAATTTTTGTATT	8850
rs572370307	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20048584	TCCTGTAAGATGCCT[A/G]GGAGCAGTCAGCACA	8850
rs572385399	in-del	-/C	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20040837	GCCCAGCCCGCGGGA[-/C]CCCCCTCCCCCTCCC	8850
rs572391157	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20056080	TCAAATTAGATTTCC[A/G]GTTTGAAGTGACCCC	8850
rs572405628	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20142584	AGAGAGAGAGAGAGA[A/G]AACTAGTATAGTTGG	8850
rs572406367	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20105710	GTTGAGGTGGGAGGA[C/T]TGCTTGAGCCCGGGA	8850
rs572427482	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20043028	ACATCAGCCTCTTGA[A/G]TAGCTGGGACTACAG	8850
rs572482238	snp	A/G	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20078206	AATAAATAAATAAAT[A/G]AAAAGGCAGCCTGTT	8850
rs572494444	snp	C/T	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20054624	TTGTGCAGCTTTTTG[C/T]GAGGTTTGTGTGGTA	8850
rs572520057	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20085619	GGGTTCAAGTGATTC[A/T]CTTGCCTCAGCCTCC	8850
rs572525083	snp	A/T	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20079061	GCTAATTTTTATAAT[A/T]ATTATTATTATTATT	8850
rs572525771	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20149214	TTCTTTTTATCAGCT[A/C]TGTGGCCATATTTTT	8850
rs572551986	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20077556	GTTTTTGAAGACATC[A/G]TAAGCAAAAACAATG	8850
rs572612719	snp	G/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20065813	GCTGAGACTATTCTA[G/T]GCTTAAACTGTTAGG	8850
rs572656547	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20053305	TTTTGGGTGGCCAAG[G/T]TGGGCAGATTGCTTG	8850
rs572684836	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20057071	TCTTCTAGTTGGCTG[A/C]TAAGGGCCTGAACTG	8850
rs572687415	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20141904	GCACAGCGGGCTCCT[C/G]TCTCTCCCTGTCTCT	8850
rs572699723	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20118892	ATGTCTCTCATGTAT[C/T]CTCTAACATAAAAAC	8850
rs572717436	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20052928	TTGCGGTGAGCTGAG[A/T]TTGCGCCACTGCACT	8850
rs572725540	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20045283	TCCACCTCCCAAAGC[G/T]CTGGGATTACAGGTG	8850
rs572734991	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20071247	GGATTTCTAGTGCTC[A/G]ATAGCCACATGTGGC	8850
rs572754669	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20084129	GGTCTGAGAAGTTGG[C/T]ACATTTAGACAACTA	8850
rs572811710	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20060298	ACTTTTTGAAAAAAT[C/T]GTTGTTTCTTAAAAA	8850
rs572816351	snp	A/T	0.0138799	0.0821421	intron-variant	KAT2B	GRCh38.p7	3:20083248	AGATTTTTATTTTAT[A/T]TTTTAGTTTTTAATA	8850
rs572825569	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20065057	TTATCTTCTTTCTCA[G/T]CATCCATCCTGGTTT	8850
rs572828081	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20126919	AGCCTATGGGGACTG[C/T]GATCCATGCCTGTGA	8850
rs572889418	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20125805	AAAATCCACAAATGT[G/T]TATCTTATTAGAACA	8850
rs572933390	snp	C/G	0.000399281	0.0141238	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20119697	GTCCTGCCTGCAAAG[C/G]CTCTTCTGGACTTGA	8850
rs573015996	snp	C/T	3.30066e-05	0.00406229	intron-variant	KAT2B	GRCh38.p7	3:20148328	GTCCTCTTTATTCAC[C/T]TCATGCAAATATTTT	8850
rs573029489	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20058640	AGATTTTTAAAGTTC[C/T]CATAGTTTAAAAATC	8850
rs573086404	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20048145	TCTCTAAAATGCGGT[A/G]AGTGTCATAAAGCCA	8850
rs573116916	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20131760	GTAGAGATAGGGTCT[C/G]CCTGTGTTGCCCAGG	8850
rs573132100	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20047580	GACTTCTTCCATCCC[C/T]GAAAGTTTCCTCTTG	8850
rs573178352	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20086067	CTTGAGCTCAGAAGT[G/T]CGAGACCAGCCTGGA	8850
rs573180751	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20064158	ATTCCAATTTTTCAC[A/G]TGCCTGATAATTTGT	8850
rs573182121	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20125709	AAAATGCTTTACCTG[C/T]CTTTTCTGTCTTGTC	8850
rs573191261	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070234	ACTGAAAAGGACTCA[A/T]TCAAAGGCAGATTTT	8850
rs573224177	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20133589	AAGACATATTTGCTT[A/T]TTTCTGGTAATTTTC	8850
rs573242869	snp	C/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20110665	GTGACACAGTGAGAC[C/T]CTGTCTCAAAAAAAA	8850
rs573245605	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20104398	GTCATGTTGATGAGG[A/C]AAGGGAAGTAGAGAG	8850
rs573247231	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20128991	CAGCCTGGGCAATGA[C/G]AGCGAAACTCCATCT	8850
rs573258910	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20094412	TGTGGGGATTGCAAT[G/T]TGAGATGATGTTTGG	8850
rs573290128	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20067536	AAGATCTATATCTCT[A/C]AAACTCTGTGTTGTC	8850
rs573308691	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20124157	ACTATAGTTTTTTAG[G/T]GATTTAGTAACATTA	8850
rs573318127	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20088071	GTGTGAGCCACTGTG[C/T]CTGGCCATTTCCTTA	8850
rs573374331	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20103648	TCCTGACCTCAAGCA[A/G]TCCTCCCACCTTGGC	8850
rs573391841	in-del	-/AC			intron-variant	KAT2B	GRCh38.p7	3:20086263	GGGTGACAGAGTGAG[-/AC]ACTGTCTCAAAGAAA	8850
rs573432820	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20069821	GGTGTGAGCCACTGC[A/G]CCCGGCCAAGCTTTT	8850
rs573463120	in-del	-/G			intron-variant	KAT2B	GRCh38.p7	3:20151435	GGATATTGGTAGTCA[-/G]AAGTGGGGTTTTTTT	8850
rs573487039	in-del	-/G	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20132267	AATCCCAGCTACTCA[-/G]GAGGCTGAGGCAGGA	8850
rs573514595	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20082330	TTGAGCCACTGCACC[C/T]GGCCACGGTTTTCTC	8850
rs573524646	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20047805	ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT	8850
rs573531483	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20112769	TTTGATCAAAGATTG[A/G]TGAAACACTGTTTTG	8850
rs573628331	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20118595	GGGAGTTGTGGCAGG[C/G]ACCTGTAATCTCAGC	8850
rs573636497	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20093777	ACACTTAGAGCTATA[A/C]CTAAGAGGATCGTTC	8850
rs573652169	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20120620	GTAGTCTATTCCTTT[C/T]GTAGGAATAACTGCA	8850
rs573690653	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20113298	GCATTTTATGTTTTC[A/T]GGTAATAGTTGTCAT	8850
rs573746200	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20134228	TTTTTATAATACTTT[C/T]GTAAAGGTTTATTTT	8850
rs573832658	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20053475	AGGAGGTCGAGGCTG[C/T]GGTGAGCCGTGAGTG	8850
rs573838199	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20127645	TCTGTGCCATGTCCA[A/G]AGAAGGTTCAAAGTG	8850
rs573838651	snp	G/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20148975	CACAATTCTTGATTT[G/T]CCATGCCCTTGATGG	8850
rs573855277	snp	C/T			synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20101310	TAACTTTGTGCAGTA[C/T]AAATTTAGTCACCTG	8850
rs573869566	in-del	-/TTTTTTTTTTTTTTT			intron-variant	KAT2B	GRCh38.p7	3:20063550	TTTTTTTTTTTTTTT[-/TTTTTTTTTTTTTTT]GAGATGGTTGCTCTG	8850
rs573951089	snp	C/T	0.000798403	0.0199641	downstream-variant-500B	KAT2B	GRCh38.p7	3:20154514	TCTTAAGCATTCTGT[C/T]GCATTTGGGGGAGGT	8850
rs573960502	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20054193	GCAGTGCAGTGGCGC[A/G]ATCTTGGCTCACTGC	8850
rs573968973	snp	C/T	1.67122e-05	0.00289064	intron-variant	KAT2B	GRCh38.p7	3:20119772	GACTTGCTCCAGGAG[C/T]TCCATTACCTGAGGA	8850
rs574090761	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20141032	TCTATTTACTATTCT[C/T]CAAAGTGTCTTTGTC	8850
rs574106447	snp	A/C	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20079466	GCTTCAGCCTCCCCA[A/C]ATGCTGGGATTACAG	8850
rs574142026	snp	C/T	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20097750	CATTGTCGGCCACGC[C/T]TGTCTTGAACTCCTA	8850
rs574180940	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20125021	GTTCTTTAAAAAGAG[A/G]TGTTAAGAATATATA	8850
rs574182836	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20117421	ATAAATGACATTCAT[A/G]AGGATGAACCTGAAA	8850
rs574240574	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20124234	GTACTAGTCTATTGC[A/G]TTGCTACAAAGAAAT	8850
rs574242415	snp	C/G	0.00358779	0.0422022	intron-variant	KAT2B	GRCh38.p7	3:20113064	TTTTCTTTAGAGAAC[C/G]AGTACATGAGACTAA	8850
rs574246078	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20103746	AAAAATGCAAGGCAG[C/T]CTTTGAGAATTACTA	8850
rs574262990	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20110775	ATGCACTTTCTAAAT[C/T]AGATGACCTGTATTG	8850
rs574312292	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20131931	GGCACTTTAAAATCT[A/G]TATATGGTCATTTTG	8850
rs574326163	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20102008	AAAATGCAATGACCA[C/T]ATAATGAAGTTAAAG	8850
rs574339645	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20140015	AGGGCCATTTAAAAA[A/G]TGTTGTCTTGCTTCC	8850
rs574379766	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20089120	AGCATTTTGTTTTGA[C/T]TGAGATAGCTTTGTA	8850
rs574382422	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20095744	GAACAGTGGACAAAA[C/T]AGAGTTCTTCCCCTC	8850
rs574393262	snp	C/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20045401	TGTTGCCCAGGATGG[C/G]GTACACTGGCACGAT	8850
rs574395581	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20102452	ATGTAGAATTTTGTA[A/G]CCTTTATGTCTCTTC	8850
rs574403393	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20147891	AATTTCTTGTTTTTG[A/G]TAAGTATTAACTATG	8850
rs574429753	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20082968	AAACAACTCCCTGGG[C/T]CTTCCGTTGAATGCA	8850
rs574467500	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20082375	TCAATTACCAACTTT[A/G]GTAAATTTAACATTA	8850
rs574501976	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20132634	TAAACTACCATGACT[C/G]CTAGTCACAAATACT	8850
rs574503667	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20052264	CCTTTACTGCACTTC[C/T]TAATATTTGGAAATT	8850
rs574575270	snp	A/G	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20063644	GCCTCCCAGGTTCAA[A/G]CAATTCTCCTGCCTC	8850
rs574661034	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20153453	TGATACACACAGCCA[C/T]GCTGATAATATGCAA	8850
rs574664908	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20145886	GGGCCCGTTTACCTG[C/T]TTCTCTAGTCCGAAG	8850
rs574668129	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20088160	CATTTGTTGGGGTGG[A/T]CACTTAGGTAAATTC	8850
rs574679046	in-del	-/T			intron-variant	KAT2B	GRCh38.p7	3:20081009	ACTCTTAGGCTTCTC[-/T]TTTTTTTTCATTCCA	8850
rs574691255	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20082459	CAAAAATGTTCTTTA[C/T]AACATATTTTCCTTT	8850
rs574701896	snp	C/T	0.000152386	0.00872753	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152530	TTGACAAGTGATTTT[C/T]TTTCCCCTCTGCTTC	8850
rs574822424	snp	A/G	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20051754	TCCCTGAAAAGTAGT[A/G]TTGAATATATGATGA	8850
rs574824560	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20146738	AAAGCAGGGAATCCT[A/G]TTTTATAAATGGGGA	8850
rs574841435	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20099633	CTTCATAACTCTGGC[C/T]GTGGACATGAAGGCC	8850
rs574844293	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20073669	CAATACAGAGCAAAA[A/G]TTTCAAAAGTTAGAG	8850
rs574846276	snp	A/G	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20062542	TCTCGGCTCATTGTA[A/G]CGTCTGCCTCCTGGG	8850
rs574878287	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20083954	AGGTGGGGTTCGGGG[A/G]AGATTGGAGCTGGAG	8850
rs574885408	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20108585	CAAATACTTACCATT[A/C]TGTTACAGTCGTTTG	8850
rs574900308	snp	A/G	0.00159617	0.0282053	intron-variant, nc-transcript-variant	KAT2B, MIR3135A	GRCh38.p7	3:20137606	CAGTGGTGCAATCTC[A/G]GTTCACTGCAGCCTT	8850
rs574901203	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20139112	TTGGGAGAGAATCTT[G/T]CTATGTTGCCTGGGC	8850
rs574933515	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20043832	ACTTAATATGAGCAA[A/G]CCCAAAAGGACAGAT	8850
rs574963221	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20075745	CTCCAGGTGCACGAC[A/C]CCCCAGGCACCTCCA	8850
rs574977647	snp	A/C	0.206947	0.246265	intron-variant	KAT2B	GRCh38.p7	3:20118755	AAAAAAAAGAGAGAG[A/C]GCGAACTATATATAT	8850
rs575007502	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20086892	ATTCAAGTCATTCTC[C/T]TGCCTCAGCCTCCCA	8850
rs575038040	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20117924	TGTCAAACTCACAGA[A/G]TTACAAGAAGAGGAC	8850
rs575077599	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20044703	ACTCAGATTCCTTGC[C/T]TTTCCTTTACCCCCC	8850
rs575086110	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20125097	GGAGGCCGAGGCGGG[C/G]AGATCACGAGGTCAG	8850
rs575109378	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20076651	TACATTTGCCAATTT[C/T]GTTGTATCTAACCCC	8850
rs575117183	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20094214	CTTACAATCATGGTG[A/G]AAGGTGAAGGAGAAG	8850
rs575118037	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20144540	GTGATCTGCCCACCT[C/T]GGCCTCCCAAAGTGC	8850
rs575138195	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20132729	GGAAAAGATTTTTGG[A/C]GAGATGGCAAATTTG	8850
rs575146647	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20133518	CTACTTTATTCTTTT[C/T]ATACAGTATTTTATA	8850
rs575168989	in-del	-/TT			intron-variant	KAT2B	GRCh38.p7	3:20107049	TTTTTTTTTTTTTTT[-/TT]GAGACGGAGTCTTGC	8850
rs575172601	snp	C/T	1.65375e-05	0.0028755	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20122766	ATCAACGAGGTTATG[C/T]CTACCATCACGGACC	8850
rs575183889	in-del	-/TTGAC	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20151459	TTTTTTTTTTCCCAT[-/TTGAC]TTATTTTTCCACACA	8850
rs575186402	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20089266	CTATTTCTGTGAAAA[A/G]TGTCATTGGAATTTT	8850
rs575208233	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20113510	GCTTATGCTAGGAGC[C/T]AAAACATCAATGCTG	8850
rs575213862	snp	C/T	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070465	GCCTGCCACCACGCC[C/T]GGCTAATTTTTTGTA	8850
rs575222827	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20088220	AGTGAATATGGGAAT[G/T]CAGATGTCTTTTTGA	8850
rs575227086	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20063318	CAGCGTGCTGGGATT[A/G]TACACCTGAGCCACC	8850
rs575228065	in-del	-/ACAG	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20075663	TAATATAAAGGATAC[-/ACAG]ACAGCCAGATGAAGG	8850
rs575274585	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039664	AAGAGAAAGGGAGAA[A/C]ATCACGTCTTTATTT	8850
rs575385158	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20095816	ATAATACCTTTGCAG[G/T]TGGTGATAAGTGTTG	8850
rs575394508	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20045197	TTTTTGTATTTTTTT[C/T]GGTAGAGATGGGGTT	8850
rs575439168	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20138471	TTTGCCCTCATTGAT[A/G]GTAATTTGCTTAGAA	8850
rs575439484	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20093395	TTAGTCTTTGGCTAA[A/G]AGCTGCTCTTGAGGG	8850
rs575455600	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20044837	ATCTTTGAATAGATT[A/C]TTAGCCATGCGGTTA	8850
rs575487562	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20135501	CTACTAAAAATACAA[A/G]AAATTAGCCAGGTGT	8850
rs575494258	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20147710	TGTACATATTTATTT[G/T]TTATGCTCTCCACTG	8850
rs575518014	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20096291	CTCTTCACTAGTTCT[A/G]CCTCAGCTCCATGTG	8850
rs575582513	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038333	ACTGTGAAAATTTTC[A/T]AACATACAGAAAAGT	8850
rs575585965	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20047163	CTCAGGTGGTCCTCC[C/T]ACCCTAGTCTCCCAA	8850
rs575599490	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20075806	TAATCCCAGCTACTT[A/G]GGAGACTGAGGCATG	8850
rs575611537	snp	C/T	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20144603	CAGGTTTCTTTTTTC[C/T]TTTTTTTTTTTAAGA	8850
rs575623433	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20078556	TTTTTTTTTTTGTAT[C/G]TTTGGTAGAGACGGA	8850
rs575634021	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20080092	GTTCTTATTTCCATT[C/T]CTGCATACCTGGCTT	8850
rs575635992	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20059678	CCACTGCATTCCAGC[C/T]TGGGCGACTGAGCGA	8850
rs575647705	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20102554	ACCATTTCTCTATTG[C/T]TGGACATTCAAACTC	8850
rs575650911	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20046276	GTACAGGACTATAAA[A/G]TTAGTCTTAATTGAA	8850
rs575661110	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070525	TAGCCAGGGTAATCT[C/T]GATCTCCTGACCTCG	8850
rs575677897	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20117288	TTAGTATTACCTGAA[A/G]CCATCAGAAGTGGGC	8850
rs575679905	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20109418	AACTCCTAGGTTCAA[C/G]TGATCCTACCTCCTC	8850
rs575700735	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20129176	AATATGAGGTTATAA[A/G]AGCACACATATTATG	8850
rs575706741	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20130925	GTGTGTGCATGCGTG[C/T]GTGTGTGTGTGTGTT	8850
rs575814426	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20075309	ATAAAACTTTTTTCT[A/G]TTTTACTCAACACAG	8850
rs575814443	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20130411	TGACAAATGTCCAGA[C/T]GTTTCCAAATGTTCA	8850
rs575816842	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20051580	CAATGCCACCTTTCT[C/T]ATGTGGGCCTAGTTG	8850
rs575891961	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20123286	CTAACTATTTTTGCA[G/T]GTACTGTATCTCATA	8850
rs575943605	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20056503	GTATTTAGTAACTTG[A/G]TATAGAATCTGGGAC	8850
rs575955278	snp	A/T	0.00318978	0.0398085	intron-variant	KAT2B	GRCh38.p7	3:20087895	TCCTCTTGCCTTAGG[A/T]TGCTAAGTAACTAGG	8850
rs575964563	snp	C/T	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20151620	GGATTGAAGAAACCC[C/T]ACTTTAGTTTTATCA	8850
rs575991732	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20116643	TTTTTTCTGTATGTC[G/T]TTTCATCTCCTGTGA	8850
rs576004720	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20056008	TTCTGCTGTATGGAC[A/G]TACTAGTTTGTTTAT	8850
rs576163059	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20073789	ATGGAGTTTAGGATT[G/T]CCTCAGGAAATGTGA	8850
rs576164567	snp	A/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20094994	CCAGTACTGATTCTT[A/T]AAATATACATTATTT	8850
rs576176331	snp	A/C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20121531	TGTGGAATGGTGAGA[A/C/T]TGCATCTACTTGATA	8850
rs576252425	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20108340	GCTGGTGGCTACTGT[A/G]TTGGATAGCAGAGAC	8850
rs576255583	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20144099	ACGCCTCCCATTCCC[A/G]TTAACAGTCACTTCT	8850
rs576292107	snp	A/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20107431	GGGAGGCCAAGGCGG[A/T]TGGATCACTTGACGT	8850
rs576300478	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20042428	GCTATGTACAGAATT[A/G]AGAACAAGGTCATGG	8850
rs576336609	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20105403	CTGAAGGAAAGTGCA[A/G]GTAATTAGTCTTAGA	8850
rs576337318	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20065984	ACAAATAACCACAAA[A/G]TATGTGGCTTAAAAC	8850
rs576344888	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20128606	GGTGTCGCAGTCTGG[C/T]GAGAATAAACCAGAC	8850
rs576367632	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20079706	GTACCATATAATTGC[C/T]CCCTCAGTTCCCATT	8850
rs576379144	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20109050	GGTTCTACCATCTAG[G/T]TTTGTGTAGGTACAC	8850
rs576389820	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20135864	GTAGAACTAAGGTCA[A/G]TAAGTAGAAATAACA	8850
rs576416504	snp	A/G/T	0.00239393	0.0345281	intron-variant	KAT2B	GRCh38.p7	3:20138570	GGGGGTCAGGAAAGG[A/G/T]GTTGGTAACTGAAAA	8850
rs576427764	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20086282	TGTCTCAAAGAAAAC[A/G]AAAACAAAAAGGAAG	8850
rs576436824	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20056126	AAGAATAAAGTATAT[A/G]AGAGAAACAGTAGAT	8850
rs576467751	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20043057	AGGCATGCGCCAGTA[C/T]ACTATTATTATTATT	8850
rs576557149	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20131101	GCTCACTGCAAACTC[C/T]GCCTCCTGGGTTCTG	8850
rs576575079	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20054728	GCATCAGCTCTGACA[A/G]GCTGGTGTTGAAACT	8850
rs576587559	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20060357	CTGTAGTCCCAGTAC[C/T]TTGGGAGGCCAAGGC	8850
rs576643237	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20054360	TCTTGAATTCCTGAC[C/T]TCGTGATCCACCCTC	8850
rs576690724	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20142629	AGTGGAGAGTTAAGT[A/G]CTACTTTGTGAGTGT	8850
rs576713393	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20076221	TATATTTCATACTAT[A/G]CCACAAACATGTATT	8850
rs576730508	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20109180	ACAGATAGTCTTGTG[A/G]TTGCCTAAGTCTCAC	8850
rs576785896	snp	C/G	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20145641	TTAATAATTATTTTA[C/G]AAAACAAACAAAACA	8850
rs576790893	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20095095	TTAATTATAGGTAGA[C/T]TTTGTGAGAAGACTT	8850
rs576812822	snp	A/C	0.00119737	0.0244387	intron-variant	KAT2B	GRCh38.p7	3:20081049	TTACAGAAAATGAAA[A/C]CACTTTTAAATGATA	8850
rs576840334	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20111379	TGTATGATGCTGCAG[A/T]ATAAGGTGATTTTAA	8850
rs576844729	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20049107	CCTCGTGATCCGCCC[A/G]CCTTGGCCTCTCAAA	8850
rs576852289	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20143238	TATCGTCATGGTAGG[G/T]AGTTGAAGATATTTT	8850
rs576873050	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20151972	CTGCTCTACTCCATA[C/T]AGATAGAGCCTCTTC	8850
rs576876118	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20080403	TCTGCTTATCCTCCA[A/G]GGCTTGACTGCAGAA	8850
rs576896080	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20108739	CGGGCTGCACAGCAG[C/G]AAGTGAGTGGTGGGC	8850
rs576926857	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20057185	TGCAGATTAACCTTA[C/G]GAGCTGGGAGAAGGA	8850
rs576964377	snp	C/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20081679	CTTTGTATCAGGCTC[C/T]TGGAAGACTATTTAA	8850
rs576967787	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20115049	CCTGAAGTGTAAGTT[A/G]CAGTTCACTGCAACT	8850
rs576980206	snp	C/T	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20055943	TTTTTGAGATTAATC[C/T]GTGGTGTTGGATGCA	8850
rs576989208	snp	A/G			downstream-variant-500B	KAT2B	GRCh38.p7	3:20154624	CTTACCCACTCACCC[A/G]CTAAACAATAACAAA	8850
rs577025723	snp	C/T	1.65957e-05	0.00288055	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152369	CCTCAAGAATAGGTA[C/T]TACGTGTCTAAGAAA	8850
rs577060994	in-del	-/G			intron-variant	KAT2B	GRCh38.p7	3:20132707	TCTCACAAGCAACTT[-/G]GAATCTGGAAAAGAT	8850
rs577102128	snp	C/T	0.00159617	0.0282053	intron-variant	KAT2B	GRCh38.p7	3:20062467	ATATATTTTATTTTA[C/T]ATATATATATATTAG	8850
rs577105778	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20142721	ACATTTGTTTTGAAC[C/T]GGGCAGCCTGGTGAT	8850
rs577124691	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20122227	TGAAAATACACATTC[C/T]TTCCAAGAAGACACT	8850
rs577133936	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20086359	ATTCTAGCACTTTGG[G/T]AATCCGAGACGGGAG	8850
rs577144285	snp	A/C	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20073821	GTAATAAATGTCTGG[A/C]CTCAAGAAATCCTTA	8850
rs577234942	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20062899	TGTTGTTGAGTTGTA[A/G]GCATTCTTTATATAT	8850
rs577264803	in-del	-/TCTC	0.0197687	0.0974348	upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039776	GGGTGGAGGAAGTTG[-/TCTC]TCTGTCAGAGACAGG	8850
rs577306981	snp	C/T	0.000181868	0.00953419	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20122740	TTATGGGGGATATTC[C/T]GATGGAATTAATCAA	8850
rs577326490	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20129461	CTCACTGCAACCACC[A/G]CCTCATGGGTTCAAG	8850
rs577349331	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20143812	TGCATGTTTTCTGTT[A/G]TAAGTGGGAGCTGAA	8850
rs577382272	snp	A/C	0.0023933	0.0345097	intron-variant	KAT2B	GRCh38.p7	3:20134765	CTGTACAAATGCTGC[A/C]TAACAGGAATGTAAT	8850
rs577423304	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20135039	TGAGGCTAGTGTCTA[A/C]TCTGTTGAATAGTAT	8850
rs577426047	in-del	-/A			intron-variant	KAT2B	GRCh38.p7	3:20107656	GCAATACTATGTCTC[-/A]AAAAAAAAAAAAAAA	8850
rs577450332	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20083370	TCTTCTTAATAAAAG[A/G]TTAAGAGAAGGGTTT	8850
rs577590398	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20095561	CATGACTGATTCTCT[A/C]AAATGGCCCACCATA	8850
rs577623915	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20050311	AAAACTTTTAGTTGC[A/T]TTACACATAAAGGGC	8850
rs577629031	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20150581	ATAATTTAATGGTGT[C/G]TCTATATTTGGTACC	8850
rs577678804	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20105843	GAAGAAAAAGAATAC[A/G]TAGCAAGTTAGCTAG	8850
rs577678898	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20114078	CTGTATTTCTTTTCT[C/T]TTTTTTTCTCTTTTA	8850
rs577694521	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20041789	TGCCTGCTGTAAAGA[A/G]GGTCAAGTTCCCAGA	8850
rs577721847	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20127773	TCAGATTAGGGCTAT[G/T]ATTTTGGGATGAAAC	8850
rs577760029	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20142369	TGAAGTCACTTCAAT[A/G]AAAATATATTTGGAT	8850
rs577778916	snp	A/G	0.000798403	0.0199641	intron-variant	KAT2B	GRCh38.p7	3:20127180	TATTTGTAAACCTCA[A/G]GCACTTCTTAGGTGA	8850
rs577785573	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20066372	TTCCAAATATGGCCC[C/T]ATTTTGAGGTTCCAG	8850
rs577786625	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20111513	TCTGCTATAGTTAAT[A/G]GTACGAGATAAACAT	8850
rs577809206	snp	G/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20078344	TATTAAATTTGTCTA[G/T]TAATAATATTTTAGT	8850
rs577816752	snp	A/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20106557	ATAAGATTAATCTTG[A/G]AAGTTAAGAAAAAGC	8850
rs577849134	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20091669	CTTTTGCTGCATTTT[G/T]TAAGTTTTGGTATAT	8850
rs577849493	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20074564	CGTAGTAGTGGTACT[A/G]TAACACTATCAGGGT	8850
rs577902948	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20088951	CTAATTTCATTCTTT[A/T]GCATGTGGATATCCG	8850
rs577911999	snp	G/T	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20120760	AGAGAATGTTTTGAA[G/T]GTTGCATTTCTGTCC	8850
rs577959424	snp	A/T	0.00279162	0.0372561	intron-variant	KAT2B	GRCh38.p7	3:20085578	TGCAGTGGTGCAATT[A/T]TGGCTCACTGCAGCC	8850
rs578017449	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20049010	GAGACTACAGGCCCC[C/T]GCCACCACGCCCGGC	8850
rs578150928	in-del	-/TATA/TATATA	0.0554779	0.157039	intron-variant	KAT2B	GRCh38.p7	3:20142873	GCAAGCATAATTGGG[-/TATA/TATATA]TATCTATGTGCCTGT	8850
rs578152514	snp	C/T	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20148547	TGGCGGTGTGGGGGA[C/T]AAATGGTTGCTGAGG	8850
rs578185076	snp	C/G	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20097333	TGCTTTAAAGTACAT[C/G]TTCTCTCTCTTTCTT	8850
rs578188415	in-del	-/TT			intron-variant	KAT2B	GRCh38.p7	3:20134874	GAAATTAATTTTGAC[-/TT]TTTTTTACTTAATAT	8850
rs578211750	snp	A/C	0.000399281	0.0141238	intron-variant	KAT2B	GRCh38.p7	3:20064886	ATATTTTAAGCATGA[A/C]AGAATTTTGCTAGAC	8850
rs578214884	in-del	-/TCT	0.00199481	0.0315187	intron-variant	KAT2B	GRCh38.p7	3:20075945	TCATACGGCTTTATC[-/TCT]TCTACACTTTCCCTC	8850
rs745333451	snp	C/T	1.94165e-05	0.00311575	intron-variant	KAT2B	GRCh38.p7	3:20152312	GTCAAAGATTGCTAA[C/T]ATTTTTTTTTCCTGT	8850
rs745348936	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20083984	GAAGAGGTTAGCTGG[G/T]GATGTGTATTTGTTG	8850
rs745351901	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20095994	CTGTGCAAAGTGCTA[A/G]GGGAAGAGACTCCGA	8850
rs745370505	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20055231	ACAAGCCTCAGATTT[A/C]GCAGCTGTAATGTGG	8850
rs745373528	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20060202	AGGCATCTGCATGCA[A/G]GTCTTAGTATGGATA	8850
rs745373644	snp	C/T	1.75922e-05	0.00296577	intron-variant	KAT2B	GRCh38.p7	3:20148495	CCCCATGGGTAATAC[C/T]ATTAACATTTTCTAA	8850
rs745380519	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20109381	CATTGCAGTGGCACA[A/G]TCATAGCTCACAGCA	8850
rs745477049	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20130910	GGTAAGAACGTGTGT[G/T]TGTGTGCATGCGTGC	8850
rs745505915	snp	A/C	1.90366e-05	0.00308511	intron-variant	KAT2B	GRCh38.p7	3:20099823	ATAGACATACCAATT[A/C]AGTTTTTCTTTTTCT	8850
rs745549960	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20066967	ATTTTTAAAGACTCC[A/G]TATTCGCTTGTGGCT	8850
rs745576978	snp	A/G			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039305	TTTTTTTTTCTTTTT[A/G]AAGTTTGAGGCCAAA	8850
rs745586353	snp	A/G	4.98923e-05	0.00499436	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20095363	TACCTGTGTCCACAA[A/G]GAAGAAGATGCAGAT	8850
rs745595746	snp	A/G	1.64792e-05	0.00287042	intron-variant	KAT2B	GRCh38.p7	3:20072325	CTCTTTCTTTATTCC[A/G]TTTTTAGGCCGAGGA	8850
rs745597798	snp	A/G	1.65334e-05	0.00287514	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20114914	AAGAAGAAGTATATA[A/G]TCAAAACTCTCCCAT	8850
rs745603833	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20148127	GTTTTGAGTTTCCTA[A/G]AACATTCTGGAATGG	8850
rs745604869	in-del	-/T			intron-variant	KAT2B	GRCh38.p7	3:20113676	TGTTGAAGCCTGAGG[-/T]TATTATTTGAGTCTT	8850
rs745625014	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20104977	TGCAACCTCCACCTC[C/T]TGAGTTCAGGCGATT	8850
rs745628527	in-del	-/T	7.44969e-05	0.0061027	intron-variant	KAT2B	GRCh38.p7	3:20099837	AAGTTTTTCTTTTTC[-/T]TTTTTTTTAATGATT	8850
rs745647726	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20076469	TTTATTGGTCTTAGT[A/G]TAACAGCTCTAGAAA	8850
rs745649964	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20077638	TATTTTGAATATGTT[A/G]GGTTAATGTATTATT	8850
rs745666955	snp	C/T			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038654	TATCTGTTAAATCCA[C/T]GTTAGAGGTTGATCA	8850
rs745690367	in-del	-/C			intron-variant	KAT2B	GRCh38.p7	3:20064972	TCTCACTCATTAACA[-/C]TGCGTGAACTGTGAG	8850
rs745711377	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20128700	AAAGGGAACCAGAAA[A/G]CATGTCCTTAGAATG	8850
rs745738862	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20116694	GAGACCCAGTTTTGT[C/T]ACAATAATTGATACA	8850
rs745741421	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20049345	TGGTATTAGCAGTTT[A/G]TGTGTTTGCCAAAGT	8850
rs745753374	in-del	-/TTTTCTTT			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20069525	TTTTCTTTTCTTTTC[-/TTTTCTTT]TTTTTTTTTTTGAGA	8850
rs745776071	snp	C/G	1.7306e-05	0.00294155	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20137070	TGGTTTCTCACCACG[C/G]AACACTGTTTTGTCA	8850
rs745793840	snp	C/G	1.73748e-05	0.00294739	intron-variant	KAT2B	GRCh38.p7	3:20111808	GGAGAGTTTTTGCTG[C/G]TCTTTGTTTGATCCC	8850
rs745830913	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20059684	CATTCCAGCCTGGGC[G/T]ACTGAGCGAGACTCC	8850
rs745853401	in-del	-/TC			intron-variant	KAT2B	GRCh38.p7	3:20140500	GTTATCTAGATTTCT[-/TC]TCTCTCTCTTTTTTG	8850
rs745879383	snp	A/G	1.67005e-05	0.00288963	intron-variant	KAT2B	GRCh38.p7	3:20101507	CTTTGGCCCCATAAA[A/G]CCTGTTACAGACCTA	8850
rs745925948	snp	A/C			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20071213	TTGCAACTACAGTGC[A/C]CTTTGATTTGAACTA	8850
rs745950332	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20058186	TATTCAGCCAGGTGC[A/G]GTGGCTCACGCCTGT	8850
rs745967071	snp	A/G			utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20153284	TTGCTTATGCAGGCC[A/G]TAAGTTCCAAAAGAT	8850
rs745973836	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20065864	GCTTGGGGGTGGAGT[C/T]CCTTTATAGTCTAGT	8850
rs745977347	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20085712	GACAGGGTTTTGCCA[C/T]ACTAGCCAGGCTGGC	8850
rs745993314	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20110576	TGTTTGGCAGGCTGA[A/G]GTAGGAGGGTCACTT	8850
rs746000789	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20139443	TCTCAGCTATGGTTC[C/T]TAAATGACTTGTCTG	8850
rs746019614	in-del	-/TATTTATT			intron-variant	KAT2B	GRCh38.p7	3:20045322	TGCACCTGGCCTATT[-/TATTTATT]TATTTATTTATTTAT	8850
rs746083122	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20109421	TCCTAGGTTCAAGTG[A/T]TCCTACCTCCTCAGC	8850
rs746086370	snp	A/G	3.38656e-05	0.00411481	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20126036	GATCCTGATGTGGCT[A/G]GTTGGCCTACAGAAC	8850
rs746113235	snp	A/C	1.65891e-05	0.00287998	intron-variant	KAT2B	GRCh38.p7	3:20125898	TTTCCTGTCTCTTGC[A/C]TCTCAGACCAATTTT	8850
rs746123398	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20043005	CCCTGGGCTCAGGTG[A/T]TCCTCCTACATCAGC	8850
rs746135373	in-del	-/TAA			intron-variant	KAT2B	GRCh38.p7	3:20043728	CAGATTTGCTTTTTT[-/TAA]AAAAAAAAAAAATTT	8850
rs746201534	snp	C/T	1.66626e-05	0.00288635	intron-variant	KAT2B	GRCh38.p7	3:20119763	GAGGGCTGTGACTTG[C/T]TCCAGGAGCTCCATT	8850
rs746218825	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20103605	ATAGAGATGGGGTCT[C/T]GCTGTGTTGCCCAGG	8850
rs746224461	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20052033	GAATCAAGTCTTTTA[C/T]AATTTTGAATCACAT	8850
rs746288861	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20092016	CCTAGAGAAAATTTC[A/T]TGTGCACTTGAGAAG	8850
rs746295346	in-del	-/T	1.77333e-05	0.00297764	intron-variant	KAT2B	GRCh38.p7	3:20148502	GTAATACCATTAACA[-/T]TTTTCTAAGTATAGA	8850
rs746312356	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20064022	TGTCAAAATCATTTG[A/G]CCATTATCTGTGAGG	8850
rs746335151	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20147718	TTTATTTTTTATGCT[C/T]TCCACTGAAAGGTTG	8850
rs746343951	snp	C/T	1.91518e-05	0.00309443	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20040749	CGCGGGCCAAGAAAC[C/T]GGAGAAACTCGGAGT	8850
rs746348152	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20144871	CACAACCTTGGTTCA[C/T]TGCAACCTCCACCTC	8850
rs746377893	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20114722	GTATTTGAATATACC[A/G]GGGCTGCCCAACTAA	8850
rs746401515	snp	C/T	0.000382482	0.0138237	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20040644	CCTGCGGTCCGGCGA[C/T]GGCAGTGGCTGCAGC	8850
rs746422235	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20074630	AGCTTAAATAAGAAA[A/G]CAATGCATATAAGAA	8850
rs746474530	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20073641	CAATGTGAGCTCTGA[C/G]TTTTGAAGCACTCAA	8850
rs746474785	snp	A/T	1.78844e-05	0.0029903	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20137092	GTTTTGTCACTCCTT[A/T]TCTTAATATGTTCTC	8850
rs746507398	in-del	-/A			intron-variant	KAT2B	GRCh38.p7	3:20042298	CTGAAGAAGGAATGC[-/A]AAAAAAGATGAAGTG	8850
rs746528275	snp	C/T	1.68846e-05	0.00290552	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20136937	GTATACTAACTTCCA[C/T]ACAGGGCTATGGAAC	8850
rs746544260	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20112000	ACTGCCGTCATTGCT[C/G]CCTTATCCCCTCCTC	8850
rs746611755	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20046383	GCTCACGAGTTCGAG[A/G]CCAGCCTGGGCAACA	8850
rs746636297	in-del	-/AG			intron-variant	KAT2B	GRCh38.p7	3:20120657	CATAGCAAAGAGTGT[-/AG]ATACCAGGAGGGTAA	8850
rs746671186	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20096171	TCTCTAATGCTTTAA[G/T]AGGAGAAATCAACAT	8850
rs746684361	snp	A/G	1.74306e-05	0.00295211	intron-variant	KAT2B	GRCh38.p7	3:20101250	AATTAGTATGATTGC[A/G]TAGCTGCATGAAGAA	8850
rs746722217	snp	A/G	3.34879e-05	0.0040918	missense, utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152347	ATCTGAAAACCATGA[A/G]TGAACGCCTCAAGAA	8850
rs746728029	snp	C/T	1.75456e-05	0.00296184	intron-variant	KAT2B	GRCh38.p7	3:20148050	GATTTTTTTTTTTCC[C/T]CACCAAGCAACTTAA	8850
rs746751999	snp	A/G			intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20136192	TATTTGGGTCTGGAC[A/G]CTTGGATTTACTTTT	8850
rs746774379	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20081218	TCCAGAGGAGCAGGG[A/G]CATGTTAGCTGCCTG	8850
rs746842830	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20131076	GCTGGAGTGCAATGG[C/T]GTGATCTCGGCTCAC	8850
rs746879043	snp	C/T			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039508	TTTAGACAATCTTTC[C/T]TTTAGCAACCAGCAC	8850
rs746884798	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20078634	TCTGCCCACCTCGGC[C/T]TCCCGAAGTGCTGGG	8850
rs746909644	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20117414	AACTGTGATAAATGA[C/G]ATTCATAAGGATGAA	8850
rs746920071	snp	C/T	1.64882e-05	0.00287121	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20119607	GGGCAGTTATCAATC[C/T]ACCTCCTGTGGCTGG	8850
rs746964628	snp	A/C	1.64811e-05	0.00287059	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20072405	CCCAGAGCCGACCTG[A/C]AGCAAATAATTGTCA	8850
rs746964985	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20049830	TTCTCTGTTGAAGAA[A/G]GATGAAAGAGACACC	8850
rs746974406	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20090281	TTTCTTGTTCTTAAT[C/G]TTAAAGGAAAAGCTT	8850
rs746987441	in-del	-/TTT			intron-variant	KAT2B	GRCh38.p7	3:20089400	TCGTGTCTTCTTCAC[-/TTT]TTTTTTTTTTTTTTT	8850
rs747019337	in-del	-/A			intron-variant	KAT2B	GRCh38.p7	3:20147162	TTAATAAACAAAATC[-/A]AACAAGCAAAAATTT	8850
rs747024644	snp	A/G	1.91676e-05	0.00309571	intron-variant	KAT2B	GRCh38.p7	3:20040791	GCAAGGTACGCGCTC[A/G]CCGCTCTCGGACCGC	8850
rs747030487	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20100453	CCGTTTTACTCAGGG[A/C]ATCTGTTAAAATGTA	8850
rs747047342	snp	A/T	1.65296e-05	0.00287481	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20146395	GTTTTAAAGATGGAG[A/T]TCGACAGATTCCTAT	8850
rs747063938	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20089568	ACCATGCCCGGCTAA[C/T]TTTTTTTATCTTTAG	8850
rs747128011	in-del	-/CTGTACAGCAAG			intron-variant	KAT2B	GRCh38.p7	3:20096066	AGCTTGAAGTGATGT[-/CTGTACAGCAAG]GAGGGCAGCGTGGTG	8850
rs747138172	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20127964	GCCTGCCACTCACCT[C/T]GTGCTGTGCAGCCCG	8850
rs747142728	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20068066	CAGTGGCGCAATCTT[A/G]GCTCACTGCAACCTC	8850
rs747167749	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20059760	ATTTAGGTACCATAA[C/T]ATTCTCTAGTTTTAA	8850
rs747173115	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20099523	CAATGGAAAGCCAGA[A/G]ACAGTGGGGAGAAGA	8850
rs747205285	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20140711	TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA	8850
rs747248565	snp	C/G	3.29913e-05	0.00406135	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20111657	CGGTACGAAACCACA[C/G]AGGTGTTTGGGAGAA	8850
rs747283018	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20044859	ATGCGGTTATTGACT[A/G]AGCGAATGAACCAGA	8850
rs747287869	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20110884	TGCAGTGATGCTGAG[A/G]TGCATTTTTGACTTT	8850
rs747290840	snp	G/T			utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20153482	AAATGAACATTTTCC[G/T]TTATGTCTCTCCAGA	8850
rs747303391	snp	A/T	3.49608e-05	0.00418081	intron-variant	KAT2B	GRCh38.p7	3:20099845	TCTTTTTCTTTTTTT[A/T]AATGATTTCTTTGCA	8850
rs747308010	snp	C/T	1.65512e-05	0.00287669	intron-variant	KAT2B	GRCh38.p7	3:20127398	CTAGGATAGGTAAAA[C/T]TTTGACATAATCTTA	8850
rs747316504	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20082426	CTACTGTTTGTATTC[C/T]AATTTTATCTGTTGA	8850
rs747341316	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20058276	CAGCCTGGCCAACAT[A/G]GTGAAACCCCGTCTC	8850
rs747376667	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20043774	TGGGTACGAGGGAGT[A/G]TAAGAGAGCAAAATC	8850
rs747383018	in-del	-/G			intron-variant	KAT2B	GRCh38.p7	3:20132348	ATTGCACTTCAGCCT[-/G]GGCAACAAGAGTGAA	8850
rs747399255	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20106067	CCCTGTGAACTAGGG[C/T]AGATCAGTTTATTCC	8850
rs747429331	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20134087	TACTTATGGTGCCTT[A/G]AAGACGTTTTAAAAT	8850
rs747467554	in-del	-/CA			intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20135653	AGCAAGACTCCATCT[-/CA]AAAAAAAAAAAATAA	8850
rs747506090	snp	C/T	1.65723e-05	0.00287852	stop-gained, nc-transcript-variant	KAT2B	GRCh38.p7	3:20122721	GAGGCCAAGAAACCC[C/T]GAGTTATGGGGGATA	8850
rs747512926	snp	C/G	1.65293e-05	0.00287479	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20146394	TGTTTTAAAGATGGA[C/G]TTCGACAGATTCCTA	8850
rs747515491	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20133034	CTCTAGTTAAAAAAA[G/T]TTTTTTAGAAATAAT	8850
rs747542278	snp	A/T	1.67528e-05	0.00289415	intron-variant	KAT2B	GRCh38.p7	3:20146460	TCTTTTAAAAGCGAA[A/T]TTTTTTAGTAATGCC	8850
rs747550075	snp	C/T	4.95143e-05	0.00497541	intron-variant	KAT2B	GRCh38.p7	3:20072286	AAAACCATCAGTCCA[C/T]GGCTGCCTGTTAAAT	8850
rs747596631	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20064163	AATTTTTCACATGCC[C/T]GATAATTTGTTATTG	8850
rs747597090	snp	A/G	0.000198406	0.0099581	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20119624	CCTCCTGTGGCTGGG[A/G]CAATTTCATACAATT	8850
rs747618678	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20103432	TATTTTTTTTAGAGA[C/T]GGTGTCTTATTCTGT	8850
rs747638574	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20146258	CATTAGGTTGACTGA[C/G]TTGAACTGTATCCAT	8850
rs747647666	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20144984	GTATTTTTAGTAGAA[A/G]TGGGGTTTCACCGTG	8850
rs747682483	in-del	-/ATGGCTCAGTAGGCT			intron-variant	KAT2B	GRCh38.p7	3:20073030	TAATCATTGTCAGTG[-/ATGGCTCAGTAGGCT]CTGCTGCAGTCACTC	8850
rs747708774	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20048491	CCTCGGTGTTAGCCA[C/G]ATTTAATTCTGCGGT	8850
rs747733775	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20093066	TCCTTCAGGATCCCC[C/T]ACCCCTTGGTGTTTA	8850
rs747743055	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20125759	TGTGTCTCTGTGTGT[A/G]TGTGTGCACACATGT	8850
rs747749933	in-del	-/TGATTATTGGC			intron-variant	KAT2B	GRCh38.p7	3:20074528	TGGCATGTAAATACA[-/TGATTATTGGC]TGATGTTGTTCGTAG	8850
rs747786674	snp	G/T	1.70731e-05	0.00292169	intron-variant	KAT2B	GRCh38.p7	3:20115006	AAGTTTCCTTTTACA[G/T]GAATCAGAGAACAAC	8850
rs747790685	snp	C/T	1.65143e-05	0.00287348	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20140265	AACCAAATATGTTGG[C/T]TATATCAAGGATTAT	8850
rs747793909	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20114190	GTTGCCAAAACTTGA[C/G]ATCCATTTAGTTTAA	8850
rs747825753	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20086435	GAAACTTTGCGCCAA[C/T]GGAAAATACAAAAAA	8850
rs747829195	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20138978	AGCTCACTGCAGCCT[C/T]AACCTCCTGGGCTCA	8850
rs747840974	in-del	-/ATT			intron-variant	KAT2B	GRCh38.p7	3:20079058	CAGCTAATTTTTATA[-/ATT]ATTATTATTATTATT	8850
rs747845933	snp	A/G	1.8275e-05	0.00302278	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20137100	ACTCCTTTTCTTAAT[A/G]TGTTCTCAGGTAGCG	8850
rs747861358	snp	G/T	2.09496e-05	0.00323642	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20126069	TTTCTCCCACCAGCT[G/T]CCCCGAATGCCAAAA	8850
rs747918777	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20065522	AGCAGCAGCTCAGAA[A/G]ACTTGGCAGAAAATG	8850
rs747925570	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20097391	AAATATATTTGCTTG[G/T]GGAAACACAATCCAA	8850
rs747953794	snp	A/G	3.29886e-05	0.00406118	intron-variant	KAT2B	GRCh38.p7	3:20148313	CAGGTGAAGGTGGGT[A/G]TCCTCTTTATTCACC	8850
rs747959452	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20112515	ACCAAAAATTTAAGC[C/T]AAGCGGTTGGATGCT	8850
rs747970201	in-del	-/C			intron-variant	KAT2B	GRCh38.p7	3:20063441	ATTCTTTCTTTCTTT[-/C]TTTTTTTTTCTTTTG	8850
rs747999318	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20133868	AGCGCTCTGATCACT[A/G]TTGAGGTCGAACATA	8850
rs748000164	snp	C/T			intron-variant, downstream-variant-500B	KAT2B, MIR3135A	GRCh38.p7	3:20137869	AGCTCAGGCCAGGTG[C/T]AGTGGCTTATGCCTG	8850
rs748014311	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20096222	ACTTAGCCACTGTTA[C/T]CTGTTTCTCACTGAC	8850
rs748066960	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20079979	TCCTCTGGTCATGAA[A/G]TCCTGTTTGATACTC	8850
rs748071127	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20151113	TCTTTGTGTTTCTTA[A/G]CGCTTTTAGATTTTT	8850
rs748120284	snp	A/C	1.65729e-05	0.00287857	intron-variant	KAT2B	GRCh38.p7	3:20119737	AGGTAAGCTCTTAAG[A/C]GGGGATAAGAGAGGG	8850
rs748137421	snp	G/T	1.6577e-05	0.00287893	intron-variant	KAT2B	GRCh38.p7	3:20072504	AACGAGTTCATTGTA[G/T]CGTGAGACTCTTAAC	8850
rs748159042	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20149985	CATGCACTCTGATGA[C/T]GTGCAGCGATAGGTC	8850
rs748171188	in-del	-/T			intron-variant	KAT2B	GRCh38.p7	3:20101038	TTTTCTCCTTAATGC[-/T]TCAGGATTTCAGCAG	8850
rs748234979	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20051003	GCCAAGAAATCAAGA[C/G]CAGCCTGGCCAACAT	8850
rs748268188	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20051489	AGTCGGTGAGCCATG[C/G]AGAACCATACATGTT	8850
rs748276441	snp	A/G	1.65337e-05	0.00287517	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20146398	TTAAAGATGGAGTTC[A/G]ACAGATTCCTATAGA	8850
rs748276622	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20130218	TGTCTTCGACTCCTA[A/G]CACTAAGCATCAAAG	8850
rs748292958	in-del	-/T	0.000935195	0.0216038	intron-variant	KAT2B	GRCh38.p7	3:20114843	TTATCCTTACAGTAG[-/T]TTTTTTTTTAATCTT	8850
rs748337316	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20120279	GTCACCCTGGCTGGA[A/G]TGCAGTGGTGTGATC	8850
rs748338570	snp	A/C	1.93407e-05	0.00310966	intron-variant	KAT2B	GRCh38.p7	3:20040802	GCTCGCCGCTCTCGG[A/C]CCGCGGATGGGTGCT	8850
rs748362545	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20143093	GTGATGTATTGGAGA[C/T]GGGGAACTACTCCAC	8850
rs748381323	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20049684	AGGATTTTCTAGTCC[A/C]TTGAACCTGTGCAGG	8850
rs748391294	snp	C/T	1.67711e-05	0.00289573	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20111775	GAACTCTAATCCTCA[C/T]TCATTTCCCAAAGTA	8850
rs748392043	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20143099	TATTGGAGATGGGGA[A/C]CTACTCCACTGAAAT	8850
rs748400191	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20100696	TCATTGCTCTTTTAT[C/T]TGAAATTAGATGAGA	8850
rs748422252	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20099703	AGGATTTGTTTATAT[A/G]TAGTTAAGATAAATA	8850
rs748433445	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20073370	GTGGGTGACTTCTTA[C/T]GCCATCATTTCTCTA	8850
rs748438929	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20072518	AGCGTGAGACTCTTA[A/C]CTTACTGAATTCTGT	8850
rs748479035	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20090595	GAATTCAGATTGCTG[A/G]TTTTCTGTTGTGTAT	8850
rs748486245	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20113018	AACACCCAATATTTG[C/T]ACATATATTTCAACA	8850
rs748499288	snp	C/G	1.65809e-05	0.00287926	missense, utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152475	TGTGCCAATATCCTG[C/G]AGAAATTCTTCTTCA	8850
rs748574029	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20112081	CTTTTGTATATTCAG[C/T]GGCCAGGAAGCTCTA	8850
rs748587505	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20107567	GGAGGCTGGGGCAGG[A/T]GAGTTGCTTGAATGG	8850
rs748643999	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20044981	ATATAGGACAGTTCT[A/T]GGTGTCCCACAGATA	8850
rs748649858	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20122540	CTTCCTTTGTCACCC[C/G]TTCCCCTGGTGGTAA	8850
rs748653359	snp	C/T	1.66499e-05	0.00288525	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20122785	CCATCACGGACCCTG[C/T]AGCAATGCTTGGACC	8850
rs748670741	snp	G/T			utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20153719	TCTGGGAAAACCAAC[G/T]AATATACAACCATAT	8850
rs748685129	snp	A/G	1.66899e-05	0.00288871	intron-variant	KAT2B	GRCh38.p7	3:20125878	AGAATAGCTCTGTGT[A/G]ATTTTTTCCTGTCTC	8850
rs748735261	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20053367	ATAATGAGACCCCAT[C/T]TCTATAAAAATACAA	8850
rs748741630	snp	A/G	3.30874e-05	0.00406726	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20095322	AACAGACTCCTGGGA[A/G]TAGTATTGGATGTGG	8850
rs748767163	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20094312	TTTAAACATCAGATC[C/T]CATGAGAACTCACTA	8850
rs748784369	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20128634	GACTCTGAATTGACA[C/G]AAAGAGCTCTCATCT	8850
rs748796754	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20066888	TAACATTTTTTAATA[C/T]GAAGTCTTTGAAATT	8850
rs748808946	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20104810	AAAATTAAAAGCAGA[C/G]TGAACAGTAGTACTG	8850
rs748853871	snp	C/T			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038607	CATCAGTTTGACAAA[C/T]GCCTGCAAGGTGGAA	8850
rs748878422	snp	A/G	0.00014927	0.00863786	intron-variant	KAT2B	GRCh38.p7	3:20119746	CTTAAGAGGGGATAA[A/G]AGAGGGCTGTGACTT	8850
rs748888926	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20074937	ACAGCATTGATGTTT[C/T]ATGAGTATGATCCCA	8850
rs748900754	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20116249	CTTTGCATTGCTCCC[C/T]CTGTACCTGTGCTAT	8850
rs748931526	snp	C/G	1.6585e-05	0.00287962	intron-variant	KAT2B	GRCh38.p7	3:20140403	ACCTTCTGTACAGGC[C/G]AGTCTTAGCTGGGGT	8850
rs749016752	snp	C/T	1.66222e-05	0.00288285	intron-variant	KAT2B	GRCh38.p7	3:20127601	ATGTGGGGCTTCTCA[C/T]TAAGGCCTGCAGAGC	8850
rs749037829	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20044271	GGATCACTTGAGTCC[A/G]GGAATTTGAGGCCAT	8850
rs749048577	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20127674	TGGAGTTAAGGACTT[C/T]CTGGGAATAGTCCTC	8850
rs749059553	in-del	-/A			intron-variant	KAT2B	GRCh38.p7	3:20058466	TCAAAAAAAAAAAAA[-/A]AAAAAAAAAGGTTTT	8850
rs749100988	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20095000	CTGATTCTTAAAATA[C/T]ACATTATTTGCATAC	8850
rs749111004	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20067305	TGGTTTCAACACGTG[C/T]GGTTAATATTCAAGA	8850
rs749111259	in-del	-/TCTATAAGT			intron-variant	KAT2B	GRCh38.p7	3:20101537	AAAATTGTACTTGAC[-/TCTATAAGT]ATAGGGCTGCCTAGT	8850
rs749141180	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20140402	TACCTTCTGTACAGG[C/T]CAGTCTTAGCTGGGG	8850
rs749164160	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20098331	GCTTACAAATGTGGC[G/T]CTGGAGTCTAACTAC	8850
rs749171177	in-del	-/CAATT			intron-variant	KAT2B	GRCh38.p7	3:20059781	CTAGTTTTAAGTGTA[-/CAATT]CAATGATTTTTAAGA	8850
rs749199116	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20097688	ATTACAGGTGTGTGC[C/T]GCCATGCCCGGCTAA	8850
rs749210077	snp	A/G	4.94491e-05	0.00497213	missense, intron-variant, nc-transcript-variant	KAT2B	GRCh38.p7	3:20127430	TCTTTCAGGAAACAC[A/G]AAACCCTTGCTTTAA	8850
rs749217308	snp	G/T			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070100	ACTTGAGCTACTCAC[G/T]GGGGGATGTAGCTAT	8850
rs749254950	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20056557	AGTTACTGTTACAAT[G/T]AAAACAATGCTAAAT	8850
rs749261627	snp	A/G	1.98493e-05	0.00315028	intron-variant	KAT2B	GRCh38.p7	3:20099814	GAGAGAGAGATAGAC[A/G]TACCAATTAAGTTTT	8850
rs749266325	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20151949	ATGATTGAATACAAA[C/T]GTTCCACCTGCTCTA	8850
rs749266924	in-del	-/TAA			intron-variant	KAT2B	GRCh38.p7	3:20064225	TGTTTAATTGACACC[-/TAA]TAATTATACATATTG	8850
rs749288753	snp	A/G	1.69261e-05	0.00290908	synonymous-codon, intron-variant, nc-transcript-variant	KAT2B	GRCh38.p7	3:20148459	AACAGAAGCTCCAGG[A/G]TATTATGAAGTTATA	8850
rs749303614	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20081058	ATGAAACCACTTTTA[A/T]ATGATAAGCCTTTTG	8850
rs749322628	snp	A/G			intron-variant, downstream-variant-500B	KAT2B, MIR3135A	GRCh38.p7	3:20137925	GGCAGGAGGATTGCT[A/G]TGCTCAGGAGTTTGA	8850
rs749339385	snp	G/T	1.66394e-05	0.00288434	intron-variant	KAT2B	GRCh38.p7	3:20125889	GTGTAATTTTTTCCT[G/T]TCTCTTGCATCTCAG	8850
rs749392601	snp	G/T	3.34476e-05	0.00408934	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20122792	GGACCCTGCAGCAAT[G/T]CTTGGACCAGAGGTC	8850
rs749407353	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20120401	CCCTGCTAATTTTTG[A/T]ATTTTTGGTGGAGAT	8850
rs749449236	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20080273	CTTCATTGCATTTTG[A/G]CCATCAGGCTGCTCC	8850
rs749459184	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20124892	GTTTGTGGAGCATCT[A/G]CTTGCAAACCACTAG	8850
rs749472684	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20042164	TTTCTGACAAACTCC[A/C]AAGTGATGCTATGCT	8850
rs749491984	in-del	-/CTC	1.65056e-05	0.00287272	intron-variant	KAT2B	GRCh38.p7	3:20119580	ATCTAACACCTTCTT[-/CTC]CTTTTGCCGGGGCAG	8850
rs749500189	in-del	-/C			intron-variant	KAT2B	GRCh38.p7	3:20074866	TAACTCTGAAGTTTA[-/C]CCCCAAGGGAACTAA	8850
rs749510358	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20131505	AAAACTGAATGGGTC[C/T]CAGTGGCTATAGCAT	8850
rs749533667	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20091831	TAATGATTTATATAG[A/G]TTGGTCCAAAATAAT	8850
rs749538432	snp	A/C/G	3.29616e-05	0.00405954	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20072399	ACTCCCCCCAGAGCC[A/C/G]ACCTGCAGCAAATAA	8850
rs749545381	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20130497	CCTGGAAAATATGCC[C/T]TTGGTTTGTAATTTT	8850
rs749600869	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20122569	AAAGATAGAGTTGAC[C/G]TCCATGCCCATCAAT	8850
rs749605099	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20062927	TATTTTGGATATTAA[C/G]CTGTTATCAAATATA	8850
rs749608659	snp	A/G	1.86611e-05	0.00305454	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20040639	GGGCGCCTGCGGTCC[A/G]GCGACGGCAGTGGCT	8850
rs749626295	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20051653	GAACTACTTGCTGAG[A/G]CCATTAAATGCCACC	8850
rs749627099	snp	A/G	1.64838e-05	0.00287083	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20140305	ACTTTAATGGGATGT[A/G]AGCTAAATCCACGGA	8850
rs749653975	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20145119	TGATTTTCAAGAGTT[A/C]ATATGAATAAAGCAA	8850
rs749766745	in-del	-/TT			intron-variant	KAT2B	GRCh38.p7	3:20043722	TTATCTCAGATTTGC[-/TT]TTTTTAAAAAAAAAA	8850
rs749771832	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20047226	CACCATGGCCGGCTA[A/C]TTTTTGTATTTTTTA	8850
rs749799573	snp	A/C	8.29593e-05	0.00643994	intron-variant	KAT2B	GRCh38.p7	3:20101486	AATCAGATGCAAGTT[A/C]TTTTCCTTTGGCCCC	8850
rs749809492	snp	G/T	1.64882e-05	0.00287121	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20101401	TATTGGCATCTGGAG[G/T]CACCATCTCAACGAA	8850
rs749809955	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20113132	AGATTCTGAAGCACT[G/T]AAACTGCAGTTTGGA	8850
rs749819325	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20072592	ACAACAAGAGCCTCT[C/G]TAGTCTCACGAGTTT	8850
rs749850876	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20046334	TGCCTGTAATCCCAG[A/C]AGTTTGGGTGGCCAA	8850
rs749869031	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20151328	TTGGGGATATTGTAC[A/G]TACATTTACTTACCT	8850
rs749940165	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20068630	CATCCCCGGCTACCC[C/T]TAATGTAATCTCCAG	8850
rs749946851	in-del	-/CC			intron-variant	KAT2B	GRCh38.p7	3:20078171	GGTGGCAGAGTGAGG[-/CC]CTGTCTCAAAAATAA	8850
rs749959123	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20150693	TATCTATAGCTTTAG[A/G]ATAGAAAGGAAGTAT	8850
rs750021451	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20119854	AACAGCTAGAAATAA[C/G]TTTGTATTAGGCTTT	8850
rs750038094	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20079751	GCAGATGCCAAAGGA[C/T]GTAAACATGGGGCCC	8850
rs750042925	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20041378	AGGCACTGCCGCGCG[C/T]GGTGACAGCCCTGTC	8850
rs750062124	in-del	-/TT	5.065e-05	0.00503214	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152526	TTAATTGACAAGTGA[-/TT]TTTTTTCCCCTCTGC	8850
rs750075759	snp	A/G	5.11583e-05	0.00505733	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20147984	CAGGCTGGAAACCGA[A/G]TGGAAAAGAGAAAAG	8850
rs750101129	snp	C/G	1.64784e-05	0.00287035	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20072375	TGGAAAAACCCTAAC[C/G]CCTCACCCACTCCCC	8850
rs750108941	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20090932	TTTATTTTTATTTTT[C/T]GTAGAAACAGGGTCT	8850
rs750122932	snp	C/G/T	5.0225e-05	0.00501103	intron-variant	KAT2B	GRCh38.p7	3:20146456	ACCTTCTTTTAAAAG[C/G/T]GAAATTTTTTAGTAA	8850
rs750160998	snp	A/G	1.70351e-05	0.00291843	intron-variant	KAT2B	GRCh38.p7	3:20140188	GATATTTGGTGTATG[A/G]TGTTCATATGAATGA	8850
rs750194518	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20090254	AAAAGAAGTGGCAAG[C/G]GTGGGTATATTTTTC	8850
rs750198553	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20101523	CCTGTTACAGACCTA[A/C]AATTGTACTTGACTC	8850
rs750207201	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20129683	ACCCAGCCTTATACT[A/G]ACTCTTTGAAACCAA	8850
rs750253128	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20113417	ATAAATTTTTTTCCC[A/G]TAACAAATTCATTTT	8850
rs750336790	in-del	-/G			intron-variant	KAT2B	GRCh38.p7	3:20124712	GAGCTGGCTTGTACT[-/G]GAATGCACAAGAAAA	8850
rs750340080	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20073071	ACTCAAAAGGCCTGT[A/G]CTAGTATGTTGTTCT	8850
rs750355554	snp	C/T	1.65051e-05	0.00287267	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20101356	CAAACAATAGTTGAG[C/T]TGGCAAAAATGTTCC	8850
rs750406717	snp	A/G	1.66228e-05	0.0028829	intron-variant	KAT2B	GRCh38.p7	3:20127382	AAGTATATTTATATA[A/G]CTAGGATAGGTAAAA	8850
rs750422136	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20072258	ATATAATTAGTGTAC[A/G]TTGTTCTCATGTAAA	8850
rs750422887	in-del	-/C			intron-variant	KAT2B	GRCh38.p7	3:20047073	ATGGTTTTTGTTTTG[-/C]CCCCCCCCTTTTTTT	8850
rs750427240	snp	C/T	1.6489e-05	0.00287128	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20111681	GGGAGAACATTGCTT[C/T]GCTCGGTCTTCACTG	8850
rs750430063	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20084387	GCGTTTATTTCATTC[C/T]CAGAGTAAGAGCTAT	8850
rs750442381	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20089711	GGCCTACTTTCTTTC[A/G]TCAGTGTTTTATAGT	8850
rs750453204	snp	A/C/T	0.000129174	0.00803556	intron-variant	KAT2B	GRCh38.p7	3:20148535	TAAAACTCTGGATGG[A/C/T]GGTGTGGGGGACAAA	8850
rs750459426	snp	A/G			downstream-variant-500B	KAT2B	GRCh38.p7	3:20154607	TGAGTTATCCACTGC[A/G]TCTTACCCACTCACC	8850
rs750468192	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20123058	CCCAGCTTTTTATCT[G/T]GAAAAATTTCAAGCC	8850
rs750486373	in-del	-/TT			intron-variant	KAT2B	GRCh38.p7	3:20079204	CCACACCTGGCCTCT[-/TT]TTTTTTTTTTTTTTT	8850
rs750541266	in-del	-/A			intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20135655	CAAGACTCCATCTCA[-/A]AAAAAAAAAAATAAA	8850
rs750594318	snp	A/G	1.65919e-05	0.00288022	intron-variant	KAT2B	GRCh38.p7	3:20148375	TGGAATTTCCATATT[A/G]GATACCTTACTTTTT	8850
rs750603009	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20067248	ATTTTTAAGCATCAG[A/T]GTTTATTGTATGGTA	8850
rs750644312	snp	A/G	1.78541e-05	0.00298776	intron-variant	KAT2B	GRCh38.p7	3:20122638	TGTTTAGAACCACCC[A/G]TTGTTTGCCTTTTAT	8850
rs750682650	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20093638	GCAGATATTCCTCAA[A/T]AGCCTTTAGTTTCAT	8850
rs750686672	snp	A/C/G	6.64997e-05	0.00576594	intron-variant	KAT2B	GRCh38.p7	3:20095258	TTCTTTGATCTTATC[A/C/G]TAAGCTGCTCATGTT	8850
rs750725233	in-del	-/TCTT			intron-variant	KAT2B	GRCh38.p7	3:20058084	ATATGCTTTCCACTC[-/TCTT]TCTGTAGCCTTGACC	8850
rs750745091	snp	A/T			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038988	AAAATAACACAGAGA[A/T]TCTGGAAAAAGAAGA	8850
rs750754953	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20147346	TTGTGCCACGCATTT[A/G]TCTGTTTTTGTTTTT	8850
rs750755711	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20116767	CTTTTCACAAACCCT[A/G]GGAAGTTGGAATTAT	8850
rs750768174	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20104440	GAAAATTAGGAGAAT[C/G]AATATTCGGAGTAAA	8850
rs750845352	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20115829	TTTTTGTTCTTACAG[A/T]TTTGCCTTTTCCAGA	8850
rs750873507	snp	A/T	1.86635e-05	0.00305473	intron-variant	KAT2B	GRCh38.p7	3:20114844	TTATCCTTACAGTAG[A/T]TTTTTTTTAATCTTA	8850
rs750884973	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20088544	TGGCCATTTGTATGT[C/T]TTCTTTTGAGAAATG	8850
rs750896023	in-del	-/G			intron-variant	KAT2B	GRCh38.p7	3:20054495	TACATCACCTAATAT[-/G]CAGGAGGAGGTTTAG	8850
rs750924989	snp	C/G	1.66788e-05	0.00288775	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20111765	CTTGAAAAACGAACT[C/G]TAATCCTCACTCATT	8850
rs750926711	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20048916	TTGCTCTGTCGCCAG[G/T]CTGGAGTGCAGTGGC	8850
rs750936264	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20045608	AAGTATATCATCTAC[C/T]AACTTCAAAAGAGAA	8850
rs750941748	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20127160	TCTGCACATACTCTG[C/T]TCTCTATTTGTAAAC	8850
rs751031959	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20125611	TCTAAAATATTTTCT[A/C]TCTGGCCCTTCACAG	8850
rs751035241	snp	A/G			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070910	GCTACTCAGGAGGCT[A/G]AGGCACAAGAATCAC	8850
rs751052724	in-del	-/T			intron-variant	KAT2B	GRCh38.p7	3:20043329	TTCAGGAGTTACTTA[-/T]TGTGTGTGTGCACAA	8850
rs751072873	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20084774	CCCAACAAGGGAATG[A/G]GATGGGTTCTTGAGC	8850
rs751075067	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20065250	ATCTGGGTAGCTTTC[C/T]CCTCCCTGTGCCCAG	8850
rs751076329	snp	C/T	7.12771e-05	0.00596938	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152576	GCAGTGTGCCTAAAG[C/T]AAGGTGGTTTAGTTT	8850
rs751085482	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20057472	TGGTGCCAAAACAAC[A/C]GGCGGAAGGGTGAAA	8850
rs751126222	snp	C/T	1.6492e-05	0.00287154	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20101444	CCAATGATGATATTT[C/T]TGGATACAAAGAGAA	8850
rs751179221	snp	C/T	3.29908e-05	0.00406132	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20101377	AAAATGTTCCTAAAC[C/T]GCATCAACTATTGGC	8850
rs751182920	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20097278	CCTGTCAGCCTCTAT[G/T]TAGTTTATAACCAAC	8850
rs751236716	snp	A/C	1.67337e-05	0.00289251	intron-variant	KAT2B	GRCh38.p7	3:20125866	CACTGTCTTGAGAGA[A/C]TAGCTCTGTGTAATT	8850
rs751254973	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20080647	TATATTTGCAGAGGA[A/G]CTTTCAAAGTTTATA	8850
rs751263859	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20120004	GGGCTTGGTTGCAAG[C/T]TACCCATTGATTATA	8850
rs751317207	in-del	-/TGTGTGTGTGTGTGTG			intron-variant	KAT2B	GRCh38.p7	3:20121735	ACACATATGCATATG[-/TGTGTGTGTGTGTGTG]TGTGTGTGTGTGTGT	8850
rs751342912	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20092571	TATATTATATATATA[C/T]TTTATATATTTACAG	8850
rs751362933	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20054571	CCATTAAATTCCATG[A/C]CATCCTAATCAGTCC	8850
rs751463932	snp	C/T	7.56974e-05	0.00615166	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20040692	CGGGAGGCGGTGGCT[C/T]GGCCCGAATCGCCGT	8850
rs751471866	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20050941	TATGGTGGCTCATGC[C/T]TATAATCCCAGCACT	8850
rs751483553	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20144041	AATAAATTAAAAAAG[A/T]TCTCTTCTCCATACT	8850
rs751502884	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20130069	TGCAACCTCCGCCTC[A/C]TGGGTTCAAGTGATT	8850
rs751533877	snp	C/T	1.67593e-05	0.00289471	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20111773	ACGAACTCTAATCCT[C/T]ACTCATTTCCCAAAG	8850
rs751539295	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20101715	TGAGCACTTGAAAAT[A/G]TGGCTAGTTTGAATT	8850
rs751542534	snp	A/G	1.65405e-05	0.00287576	intron-variant	KAT2B	GRCh38.p7	3:20140380	GTAAGCAGGTGGTTG[A/G]CTCCCTTACCTTCTG	8850
rs751568196	snp	A/G			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070679	AATTTTATGTATGAG[A/G]TCAAAGCAGCAGCCA	8850
rs751574402	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20142981	TTCTTAAATCTTAAT[C/T]TACATGTGACAATAC	8850
rs751578887	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20072226	ACGACAAAGTCAGGG[G/T]TGAGGGGATAGCTGT	8850
rs751598511	snp	C/T	3.36146e-05	0.00409953	intron-variant	KAT2B	GRCh38.p7	3:20140207	TCATATGAATGAATT[C/T]ACTTGCTTTTCAGGG	8850
rs751656107	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20046990	GTCCAAAATATTAAT[A/G]GAATTAACAGAAGTT	8850
rs751675665	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20084525	TATTCCTTTCTACTT[A/T]GGGTTTCATACAGAG	8850
rs751686130	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20073177	TTAGTTTTTCCTAGA[A/T]ACTAAAATTTCAGTC	8850
rs751719333	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20108846	TATTGTGAACTGTGC[A/G]TGTGAGGGATCTAAG	8850
rs751755430	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20123911	GCATGCAAGGCAATG[A/T]CATTTCTTAAGACAT	8850
rs751763518	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20095616	GGCTTTTACACTTGT[A/G]TGCAAAGTTGAGTAT	8850
rs751773529	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20061508	CAGAAGTGGAATTGC[C/T]GCGTCATATAGTAAT	8850
rs751776783	snp	C/T	0.000232176	0.0107719	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152372	CAAGAATAGGTACTA[C/T]GTGTCTAAGAAATTA	8850
rs751808253	snp	C/T	6.82012e-05	0.00583917	intron-variant	KAT2B	GRCh38.p7	3:20148010	AAAAGGTAAGTATGA[C/T]GGGCAAGAGGATGTT	8850
rs751840438	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20083660	AGAGAGAACAGTCTA[A/G]GGGGCTATTTTATTA	8850
rs751850748	snp	C/T			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038317	CCCTCCCCCAATTGT[C/T]ACTGTGAAAATTTTC	8850
rs751858765	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20054887	GAGCACCGGTTAGGG[G/T]CCTGTGGCCACTTCT	8850
rs751861624	snp	A/C	1.66771e-05	0.00288761	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20099891	TATTTTACAAAGAGG[A/C]AAACCTGTGGTTGAA	8850
rs751882779	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20075670	AAGGATACACAGACA[A/G]CCAGATGAAGGGATG	8850
rs751903375	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20106217	AGTTATTTGAACAGT[A/G]AGAAAATAGCATGCA	8850
rs751907712	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20059710	ACTCCATCTCAAAAC[A/G]AAAACAAAAACAAAA	8850
rs751915602	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20107282	GTAATCTGCCCTCCT[C/T]GGCCTCCCAAAGTGC	8850
rs751927546	snp	A/C	3.30169e-05	0.00406293	intron-variant	KAT2B	GRCh38.p7	3:20072477	GAGTTCCTAAATCTT[A/C]AAGGAAAGTATAACG	8850
rs751930557	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20094712	GGGACTTTGCAGCAG[A/G]CAGTGAGGTTTTAGT	8850
rs751938694	in-del	-/TCTTTTTTTTTTTTTT			intron-variant	KAT2B	GRCh38.p7	3:20063533	ACTTCTGAGTAGGCC[-/TCTTTTTTTTTTTTTT]TTTTTTTTTTTTTTT	8850
rs751980490	snp	A/G			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039079	CATGCATAAAATCTG[A/G]TAATAAGCACATTAT	8850
rs751991240	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20105402	GCTGAAGGAAAGTGC[A/G]AGTAATTAGTCTTAG	8850
rs752008987	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20147841	CCATTAATTTCAGTC[A/G]TCTCTCAGAAGTAGA	8850
rs752060505	in-del	-/TTCTTT			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20069527	TTCTTTTCTTTTCTT[-/TTCTTT]TTTTTTTTTTTGAGA	8850
rs752068217	in-del	-/TG			intron-variant	KAT2B	GRCh38.p7	3:20114063	AGGGACTTAGGTATC[-/TG]TGTATTTCTTTTCTC	8850
rs752088443	snp	G/T	1.64795e-05	0.00287045	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20072378	AAAAACCCTAACCCC[G/T]CACCCACTCCCCCCA	8850
rs752138277	snp	A/G	1.68599e-05	0.00290338	intron-variant	KAT2B	GRCh38.p7	3:20114859	TTTTTTTTTAATCTT[A/G]TTGCTATTACTCTTG	8850
rs752151906	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20077143	GAGTGAGATAGTCTG[A/G]TCAAGTAGAAAGAAC	8850
rs752159455	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20048313	AATTTGTAGTTTTAT[A/G]TAACTGAGAAAGTGT	8850
rs752165234	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20116105	TTTCTAACCTGAGAT[C/T]GTAATTTCATGTATC	8850
rs752167932	in-del	-/TCT			intron-variant	KAT2B	GRCh38.p7	3:20076013	GTTCCAATCCTTTAA[-/TCT]TCTAATAACCTGGTC	8850
rs752185302	snp	C/T	1.65564e-05	0.00287714	intron-variant	KAT2B	GRCh38.p7	3:20140389	TGGTTGACTCCCTTA[C/T]CTTCTGTACAGGCCA	8850
rs752208523	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20060053	TCCATGTTGTAGCAT[A/G]TGTCAGCACTTCTTT	8850
rs752219297	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20096333	TTCCCTACTATAGAC[A/G]TACATCTCCTCAAGC	8850
rs752220520	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20045844	CCGCCTCATGGCATA[A/T]CAGTGAGGATTTAAA	8850
rs752243567	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20088829	CGAAGACCAATGTCA[A/G]GAAGCTTTTTCCTAT	8850
rs752260838	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20049152	GGTGTGAGCCACCGC[A/G]CCTGGCCGGGCATCG	8850
rs752263367	snp	A/G	2.46193e-05	0.00350843	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20040708	GGCCCGAATCGCCGT[A/G]AAGAAAGCGCAACTA	8850
rs752269441	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20115992	AAATCCCTACAAACC[A/T]AAGTACTAGTGAATG	8850
rs752315535	snp	G/T	1.65586e-05	0.00287733	intron-variant	KAT2B	GRCh38.p7	3:20101478	CACAAGGTAATCAGA[G/T]GCAAGTTCTTTTCCT	8850
rs752316769	snp	C/T	2.03279e-05	0.00318803	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20040630	CGGGGGCTCGGGCGC[C/T]TGCGGTCCGGCGACG	8850
rs752319109	in-del	-/C	8.36593e-05	0.00646704	intron-variant	KAT2B	GRCh38.p7	3:20040823	GATGGGTGCTAGGGG[-/C]CCAGCCCGCGGGACC	8850
rs752416354	snp	G/T	4.30635e-05	0.00464003	intron-variant	KAT2B	GRCh38.p7	3:20126119	TCTTTGACCCGTAAG[G/T]GGTACTTTCTGTTCC	8850
rs752463021	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20105359	TCACAGGATTATGAC[C/T]TCTTAAAATACAACT	8850
rs752468701	snp	C/T			utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152874	TGGGGAAATCCATAA[C/T]ATTTTCAGACCATGA	8850
rs752551864	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20121026	CTAACAAGCAGAGGG[C/T]ATATCAAGTACAAAC	8850
rs752560328	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20151769	TAAATGAAGTTTGTT[A/G]TTCTTATTTCATTGA	8850
rs752565684	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20082419	ATCTAATCTACTGTT[G/T]GTATTCTAATTTTAT	8850
rs752621802	in-del	-/T			intron-variant	KAT2B	GRCh38.p7	3:20127046	TGTAATATTTTGGAG[-/T]TAAGACTTAACTCTT	8850
rs752639876	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20132839	AATTGGATTATGGAT[G/T]AAGGGTACAAATTTA	8850
rs752667280	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20053759	ATAGACTTTCTTTAA[A/T]TGTTCCTTTACCATT	8850
rs752716676	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20054673	TACAAGGATGAGACC[C/T]GAGTAATATCATAGT	8850
rs752727779	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20073576	CCTGATCTCACAAAA[A/G]CAACACACTAATAAT	8850
rs752731931	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20051767	GTATTGAATATATGA[G/T]GAGCTCGTTATTTAA	8850
rs752733614	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20131375	ACAACTTTTGAGACA[C/T]CACACTGCCCAAGAT	8850
rs752791214	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20102621	AAAGTGGAAATTTAT[C/T]TTTATTGCTTATTAC	8850
rs752802245	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20074420	TGGACCTCAGTTTTT[C/T]CAACTCTGAAATGGG	8850
rs752820462	in-del	-/TTTTTTTTTTTTTTTT			intron-variant	KAT2B	GRCh38.p7	3:20063535	TTCTGAGTAGGCCTC[-/TTTTTTTTTTTTTTTT]TTTTTTTTTTTTTTG	8850
rs752895781	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20114583	ATGGAGGGCTGAAAT[C/T]GTGCTCTGAGATTCA	8850
rs752913448	snp	C/T	1.66657e-05	0.00288662	intron-variant	KAT2B	GRCh38.p7	3:20114869	ATCTTATTGCTATTA[C/T]TCTTGTGTCTAGATT	8850
rs752924532	in-del	-/TTTT			intron-variant	KAT2B	GRCh38.p7	3:20144795	ATTTTCATTTCTTTC[-/TTTT]TCTTTTTTTTTTTTT	8850
rs752964854	snp	A/G	1.71773e-05	0.00293059	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20137064	ACAGGTTGGTTTCTC[A/G]CCACGCAACACTGTT	8850
rs753052266	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20123959	TCTGACAGCTTCCAG[G/T]AAATGAAGAAATGGC	8850
rs753067293	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20041659	AGCAGCGGCTTTGTT[C/T]TGACAGGGTGACAGC	8850
rs753076237	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20132914	TCTTGCATCGACATC[C/T]GTGTTAAAGTGAATT	8850
rs753100543	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20054984	AAGTGAAAGAAAAAT[G/T]AAAATGAATAATCAA	8850
rs753113282	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20055797	CTAGAAAATTTCTGC[C/T]TGCTCCTTGCCATTC	8850
rs753124153	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20095899	CGAGTTGGGGACATG[C/T]CAGCGAGGAAGGTCA	8850
rs753127633	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20134533	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA	8850
rs753142128	snp	A/C/G	1.68471e-05	0.00290228	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20136938	TATACTAACTTCCAC[A/C/G]CAGGGCTATGGAACA	8850
rs753163674	in-del	-/TTTTTTTTTTTTTT			intron-variant	KAT2B	GRCh38.p7	3:20063537	CTGAGTAGGCCTCTT[-/TTTTTTTTTTTTTT]TTTTTTTTTTTTTTG	8850
rs753219240	snp	C/G	1.66396e-05	0.00288436	intron-variant	KAT2B	GRCh38.p7	3:20146440	GAATTAGTACGTATA[C/G]ACCTTCTTTTAAAAG	8850
rs753248026	in-del	-/AG	1.81145e-05	0.00300947	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20137097	TCACTCCTTTTCTTA[-/AG]ATATGTTCTCAGGTA	8850
rs753284594	snp	A/T			utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20154245	TTATGTTTTCTAATT[A/T]AAAAATTAATATTTT	8850
rs753308396	snp	A/G	1.70804e-05	0.00292232	intron-variant	KAT2B	GRCh38.p7	3:20148020	TATGACGGGCAAGAG[A/G]ATGTTAATGGAAGTG	8850
rs753357728	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20050348	CATGTTTATAGCGCA[A/G]TTAATTTTTACATGT	8850
rs753359877	in-del	-/G			intron-variant	KAT2B	GRCh38.p7	3:20135523	GCCAGGTGTGGTGGC[-/G]GGCACCTGTAGTCCC	8850
rs753433102	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20118636	GCTGAGGCAGGAGAA[C/T]AGCTTGAACCGGGGA	8850
rs753450667	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20117222	CCTATGGGAATTTTA[C/T]TCGTTTTTCTGTGGC	8850
rs753451431	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20049730	AATAAGCATTCTTTA[C/T]TACTGGCCCAGGACA	8850
rs753454376	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20088975	ATATCCGGTTGTCCC[A/C]ACAGCATTTATTGAA	8850
rs753468658	snp	A/G	2.00254e-05	0.00316422	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20040735	ACTACGCTCCGCTCC[A/G]CGGGCCAAGAAACTG	8850
rs753470482	in-del	-/C			intron-variant	KAT2B	GRCh38.p7	3:20048894	TTCTTTTTTTTGAGA[-/C]GGAGTCTTGCTCTGT	8850
rs753479283	in-del	-/TTGAGGTC	3.36496e-05	0.00410167	intron-variant	KAT2B	GRCh38.p7	3:20095225	ATGTTTGGTTTCCAA[-/TTGAGGTC]TTACATATGTTTCTT	8850
rs753509787	snp	A/G/T	6.22715e-05	0.00557965	intron-variant	KAT2B	GRCh38.p7	3:20040827	GGTGCTAGGGGCCCA[A/G/T]CCCGCGGGACCCCCC	8850
rs753515933	snp	C/G	1.65201e-05	0.00287398	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20146368	TTCGAAAAGTTTACC[C/G]TGGACTTTCATGTTT	8850
rs753529018	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20142469	ACCCCTCAAGGAAGG[C/T]AGGGATTCATGGTGG	8850
rs753546821	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20100116	TGGATCAGAGGTGTA[C/T]ACCTAATTTAATACA	8850
rs753551372	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20128596	TATTGCAGTTGGTGT[C/T]GCAGTCTGGCGAGAA	8850
rs753562073	snp	C/T	1.65266e-05	0.00287455	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20111747	GAAAAAGATAAACTG[C/T]CTCTTGAAAAACGAA	8850
rs753575197	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20072212	TGTGTATATGGCAGA[C/T]GACAAAGTCAGGGGT	8850
rs753597150	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20112599	AGAAATGAATGAGAC[A/C]GTTCATTCTGTGATT	8850
rs753623886	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20116371	ACTGGATCTCTTTTC[C/T]TCCAGACTTTCATAG	8850
rs753626059	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20142299	TCCCTCACACATTCC[A/G]TTGAATGGGTGATGG	8850
rs753627377	snp	G/T	1.65378e-05	0.00287552	missense, utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152400	TTATTCATGGCAGAC[G/T]TACAGCGAGTCTTTA	8850
rs753644869	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20141406	AAAAGAACAGAACTG[C/G]GGAGTACACAAAGGC	8850
rs753656116	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20083194	TATCTTGAGTTTTGT[A/G]GCAGGTTGACTGCTA	8850
rs753688266	snp	A/G	6.64695e-05	0.00576457	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20111622	ACTGCAACGTGCCAC[A/G]GTTCTGCGACAGTCT	8850
rs753739665	snp	A/T	3.30513e-05	0.00406504	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20122758	TGGAATTAATCAACG[A/T]GGTTATGTCTACCAT	8850
rs753746527	snp	C/T	1.65403e-05	0.00287574	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20101322	GTACAAATTTAGTCA[C/T]CTGCCAGCAAAAGAA	8850
rs753753399	snp	G/T			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20071157	AAACATTGTTAATGA[G/T]GTATTTTATATTTTG	8850
rs753775668	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20044551	TATCTGTGGCTCCTT[A/G]TCGAGGGTTCAGGCA	8850
rs753865068	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20052703	CCGGGCACGGTGGCT[C/T]ATGCCTGTAATCCCA	8850
rs753874278	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20057799	CTAGGCTATTTGGTA[A/G]CAACTGGAGCCATTC	8850
rs753883880	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20043655	CCACCGGCTGGGGTG[C/T]GTGGCCAAGAGGGCA	8850
rs753971896	snp	A/G	1.65086e-05	0.00287298	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20119705	TGCAAAGCCTCTTCT[A/G]GACTTGAGGCAAACC	8850
rs753979254	snp	C/G	3.36095e-05	0.00409922	intron-variant	KAT2B	GRCh38.p7	3:20095232	GTTTCCAATTGAGGT[C/G]TTACATATGTTTCTT	8850
rs753991358	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20145389	TGTTTAACTGTTAGG[A/G]TTACATATTCATGCT	8850
rs754006312	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20065077	CATCCTGGTTTCTGC[A/G]TACTATAACAACATC	8850
rs754019198	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20115711	AGTAATGACCACTGC[C/T]ATCAAAATATAGAAC	8850
rs754025728	snp	A/G	1.65124e-05	0.00287331	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20140361	CATTAAAAAGCAGAA[A/G]GAGGTAAGCAGGTGG	8850
rs754030761	snp	A/G	3.30434e-05	0.00406455	intron-variant	KAT2B	GRCh38.p7	3:20072492	CAAGGAAAGTATAAC[A/G]AGTTCATTGTAGCGT	8850
rs754096979	snp	C/T	1.65211e-05	0.00287407	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20111642	TGCGACAGTCTACCT[C/T]GGTACGAAACCACAC	8850
rs754103404	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20126670	TCTACTAAAAATACA[A/G]AATTAGCCAGGCCTG	8850
rs754122213	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20103006	ACCCTTTTCCTCTCT[G/T]TCTCTTCACTTTTGC	8850
rs754175441	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20048894	TTCTTTTTTTTGAGA[C/T]GGAGTCTTGCTCTGT	8850
rs754188545	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20114649	CATATGTCTGTATCC[C/T]GTGCTGTGTTAAGCT	8850
rs754201882	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20050110	AAGGCTGAGGTGGGA[C/T]GACTGCTTGAGCCCA	8850
rs754216246	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20044948	AATCACTTCTTGACA[A/G]CTAAGTAGAGATTTG	8850
rs754269127	in-del	-/A			intron-variant	KAT2B	GRCh38.p7	3:20146110	AGGGACAAGTAACTC[-/A]AAGATGTTTTTGTGA	8850
rs754271123	in-del	-/TG			intron-variant	KAT2B	GRCh38.p7	3:20087638	TGAAACTTTGTACTC[-/TG]TGACCAGCATCTCTA	8850
rs754273964	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20086166	AGTCCCAGCTATTTG[A/G]GAGACTGAGGTGGGA	8850
rs754302887	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20097900	GTGTCAATAATTAAA[A/G]TAAAAATGTGTTACA	8850
rs754313473	snp	A/G	8.34341e-05	0.00645834	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20099930	GGAAAAGAAACCCCC[A/G]TTTGAAAAACCTAGC	8850
rs754323730	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20097089	GGCTGTGAGGTTTGA[A/G]TCATTCAGCTCGAAC	8850
rs754342415	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20064672	CTCTTATCACCTAGA[A/G]CCTCAGCTTTCTCTT	8850
rs754352939	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20057340	TGCTTTACAGGTTGG[G/T]CTGGTTATGTGGATG	8850
rs754389731	snp	C/G	0.000147254	0.00857935	intron-variant	KAT2B	GRCh38.p7	3:20126141	TTCTGTTCCTTCTTC[C/G]TTATTTCCTTTTTAA	8850
rs754421986	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20048397	TGTGCTTGGAAATAG[C/T]GATTTGTGATATAGC	8850
rs754441060	snp	C/G	1.65748e-05	0.00287874	intron-variant	KAT2B	GRCh38.p7	3:20148368	TCCCACATGGAATTT[C/G]CATATTAGATACCTT	8850
rs754443326	snp	C/T	0.00424627	0.0458814	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20040623	CTGCCGCCGGGGGCT[C/T]GGGCGCCTGCGGTCC	8850
rs754480942	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20059095	TGCTTACAGTGGACT[C/G]CAGGTGTTGTTTTTT	8850
rs754488732	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20125711	AATGCTTTACCTGCC[C/T]TTTCTGTCTTGTCTT	8850
rs754491380	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20086370	TTGGGAATCCGAGAC[A/G]GGAGGATCACTTGAG	8850
rs754496726	snp	A/G	1.64953e-05	0.00287182	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20101448	TGATGATATTTCTGG[A/G]TACAAAGAGAACTAC	8850
rs754498235	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20113588	CTTCTCCTTTTAAAT[C/T]CTTTTCACCGAATAT	8850
rs754510646	snp	C/T	1.6736e-05	0.0028927	intron-variant	KAT2B	GRCh38.p7	3:20140213	GAATGAATTTACTTG[C/T]TTTTCAGGGTTTCTC	8850
rs754511355	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20057500	AAAAATTCTATTAGT[C/T]AGCTGGTTGTCTGAA	8850
rs754535544	in-del	-/T			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20069529	TTTTCTTTTCTTTTC[-/T]TTTTTTTTTTTTTTG	8850
rs754552709	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20138214	TTTTTTTATTTTAAA[A/T]TTTTTTCTGTTATTT	8850
rs754578482	in-del	-/TTTA			intron-variant	KAT2B	GRCh38.p7	3:20076450	GTTGGAATGCCAGTG[-/TTTA]TTTATTGGTCTTAGT	8850
rs754654855	snp	C/T	1.64762e-05	0.00287016	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20125959	GCAAGGTTGGAAGAG[C/T]GCAGGGGTGTAATTG	8850
rs754659716	in-del	-/AA/AAA			intron-variant	KAT2B	GRCh38.p7	3:20126821	GCGAAACTCCATTTC[-/AA/AAA]AAAAAAAAAAAAAAA	8850
rs754665595	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20097358	TTTCTTCCCTCCTTC[A/G]TCTTAAAATAACAGT	8850
rs754722619	snp	C/T	1.64887e-05	0.00287125	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20148281	AGCTTTACAGCACGC[C/T]CAAGAGCATCCTCCA	8850
rs754726307	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20068702	GTAGTAGGCCTCAAT[A/C]AATATTGTTGAAAGA	8850
rs754728246	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20080725	TATTGAACACTTGCA[A/G]TTTCACTAGTTTGAA	8850
rs754734829	in-del	-/TG			intron-variant	KAT2B	GRCh38.p7	3:20142887	GTATCTATGTGCCTG[-/TG]TGTGTGTGTGTGTGT	8850
rs754753642	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20108952	CCCCCAGCCATGGAA[A/G]AATTGTCTCTCATGA	8850
rs754800123	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20041879	CTATAATTTATTCTA[C/G]TAGAACATCTAGGTT	8850
rs754831947	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20120269	GTCTCACACTGTCAC[C/G]CTGGCTGGAGTGCAG	8850
rs754834262	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20081254	CTGCTGCCTGTTCAC[A/G]CTGCAGGGCATGTGA	8850
rs754847408	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20100273	TGGTGCTTTAAAATG[A/C]AGTCTTTGTCCATTT	8850
rs754867626	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20091590	AACATTAGGTTGTTC[A/G]TTTGAGATCTTTTTT	8850
rs754888600	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20051681	ACCCTCTCCCCAGGA[A/G]TGACAGTGAGAAGCA	8850
rs754938316	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20130135	GGCGTGAGCCACCAC[G/T]CCCGGCCTCAGCACG	8850
rs754962896	snp	A/G	1.67871e-05	0.00289711	intron-variant	KAT2B	GRCh38.p7	3:20114862	TTTTTTAATCTTATT[A/G]CTATTACTCTTGTGT	8850
rs755004501	snp	A/C	1.64879e-05	0.00287118	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20119608	GGCAGTTATCAATCC[A/C]CCTCCTGTGGCTGGG	8850
rs755026773	snp	C/T	8.27164e-05	0.0064305	intron-variant	KAT2B	GRCh38.p7	3:20140382	AAGCAGGTGGTTGAC[C/T]CCCTTACCTTCTGTA	8850
rs755056109	snp	A/G	1.65326e-05	0.00287507	missense, upstream-variant-2KB, nc-transcript-variant	KAT2B, MIR3135A	GRCh38.p7	3:20137015	TGAACTTCCTCACAT[A/G]TGCAGATGAATATGC	8850
rs755066402	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20142990	CTTAATCTACATGTG[A/T]CAATACAAGGAATTG	8850
rs755077493	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20062677	TTGTTTGCCAGACTG[G/T]TCTTGCATTCCTGAG	8850
rs755088472	snp	A/G/T	3.35133e-05	0.00409338	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20111774	CGAACTCTAATCCTC[A/G/T]CTCATTTCCCAAAGT	8850
rs755117207	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20100495	TGTTAGGTGTTGTCA[A/G]TATCTCTCATTAGCA	8850
rs755127564	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20047030	TGTTTTAGACAAATA[A/C]CTTTGCAGCACAGAA	8850
rs755143014	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20113571	GGTAAAACTACCACC[A/C]ACTTCTCCTTTTAAA	8850
rs755167857	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20041293	GAAGGGGAGGAAAGC[A/G]CGGGGTGGGAAGGTG	8850
rs755216745	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20123925	GACATTTCTTAAGAC[A/C]TACCTGTCTTAAGAC	8850
rs755219664	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20045831	GGAATGATGTTACCC[A/G]CCTCATGGCATAACA	8850
rs755223348	in-del	-/G			intron-variant	KAT2B	GRCh38.p7	3:20056286	TGTTACAAGGGAGGT[-/G]GGTGATGAAAAGACA	8850
rs755230758	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20112901	AAAACAACAAAAATA[A/G]AATGGTTTTCTGACA	8850
rs755233743	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20084551	CAGAGCTCTGAGGAG[A/G]GATCACATATTGCAT	8850
rs755254218	snp	A/G	3.30972e-05	0.00406786	intron-variant	KAT2B	GRCh38.p7	3:20127585	TTAGAAGAAGAGCAG[A/G]ATGTGGGGCTTCTCA	8850
rs755332489	snp	A/G	3.31983e-05	0.00407407	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20122777	TATGTCTACCATCAC[A/G]GACCCTGCAGCAATG	8850
rs755350046	snp	C/G/T	5.01855e-05	0.00500906	intron-variant	KAT2B	GRCh38.p7	3:20125870	GTCTTGAGAGAATAG[C/G/T]TCTGTGTAATTTTTT	8850
rs755377027	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20094813	GAGCTCTCCACAGGA[C/T]TTAGAGCTATACCTT	8850
rs755429982	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20054061	CCTCGGCCTCCCAAA[A/G]TGCTGGGATTACAGG	8850
rs755444571	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20130407	AAAGTGACAAATGTC[C/T]AGATGTTTCCAAATG	8850
rs755477559	snp	A/T	1.64795e-05	0.00287045	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20072386	TAACCCCTCACCCAC[A/T]CCCCCCAGAGCCGAC	8850
rs755541363	snp	A/C			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039087	AAATCTGATAATAAG[A/C]ACATTATGACCCACA	8850
rs755545429	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20147875	TTATTGTCATGCCTA[C/T]AATTTCTTGTTTTTG	8850
rs755556318	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20104675	GAACAAAGATGTGCC[A/G]AAAATGTTTGCAGTA	8850
rs755560108	snp	C/G			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038493	CTCAAAGTACAAAGA[C/G]CACCATTAGAGTTCA	8850
rs755588030	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20117131	TTGCTCAAAATTCTC[C/T]AGTCTGCTCAACTTC	8850
rs755614826	in-del	-/G	0.00262473	0.0361314	frameshift-variant, nc-transcript-variant	KAT2B	GRCh38.p7	3:20072360	GTAAATGTAATGGCT[-/G]GGAAAAACCCTAACC	8850
rs755635891	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20077203	CTAGCCTGTCTGGGT[A/G]TGGTGGTTTGTGCCT	8850
rs755636037	snp	C/T	2.25497e-05	0.00335773	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20040716	TCGCCGTGAAGAAAG[C/T]GCAACTACGCTCCGC	8850
rs755651420	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20049153	GTGTGAGCCACCGCG[C/G]CTGGCCGGGCATCGC	8850
rs755664243	snp	A/G	3.31625e-05	0.00407188	intron-variant	KAT2B	GRCh38.p7	3:20119740	TAAGCTCTTAAGAGG[A/G]GATAAGAGAGGGCTG	8850
rs755706566	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20099286	ACAGTGAAAGTTGCC[C/T]ATTTAGAGCTCTGCA	8850
rs755734041	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20075989	GTAGATTGATGGGTG[A/G]GGTTGAAGGTTCCAA	8850
rs755818467	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20114490	GTAAGAAGTTCTTAG[A/G]GCAGTGCAGGCACAA	8850
rs755832585	snp	C/T	0.00128287	0.0252941	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20040633	GGGCTCGGGCGCCTG[C/T]GGTCCGGCGACGGCA	8850
rs755865540	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20057897	TTAGCAAAGGGAGGG[A/C]AGTTTCTTATTCAAC	8850
rs755873712	snp	G/T	2.17176e-05	0.0032952	intron-variant	KAT2B	GRCh38.p7	3:20152284	CAGTTTTGTCAGCTG[G/T]TGTTTAAAGGGAGTC	8850
rs755926739	snp	A/C	1.66955e-05	0.0028892	missense, intron-variant, nc-transcript-variant	KAT2B	GRCh38.p7	3:20148422	ATCAAAGCGCTTGGC[A/C]CTTCATGGAACCTGT	8850
rs755952449	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20082451	TGTTGACCCAAAAAT[A/G]TTCTTTATAACATAT	8850
rs755972428	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20110091	CTCTCTTCATTAAAG[A/G]GCTCAAAGTTCATTG	8850
rs755974321	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20084819	AGCTTTCACCTCTAT[G/T]TCATCCAGAGCAACT	8850
rs755984701	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20082198	TGCCACCATGCCCAG[A/C]TAATTTTTTTATTTT	8850
rs756001338	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20080829	TAATATTGCATACGT[A/G]TTGAAAGAATAATAC	8850
rs756073591	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20151772	ATGAAGTTTGTTATT[A/C]TTATTTCATTGATGG	8850
rs756102146	snp	C/G/T	6.60692e-05	0.00574725	intron-variant	KAT2B	GRCh38.p7	3:20072491	TCAAGGAAAGTATAA[C/G/T]GAGTTCATTGTAGCG	8850
rs756118685	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20064882	TCCAATATTTTAAGC[A/G]TGACAGAATTTTGCT	8850
rs756121808	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20103180	TGTATTATTGAAACT[C/T]TGCTATATTATTGAA	8850
rs756143984	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20042642	GTGTTTCTGTTCTGG[C/G]TTTATTTTAAAATTT	8850
rs756151455	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20145283	AATTTAAATTACATG[C/T]GTGGCTTGTATTATG	8850
rs756186772	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20131413	TTTTCACTGGCGTAT[A/C]GTCTAAGATAAAGAT	8850
rs756187022	snp	C/T	1.65359e-05	0.00287536	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20095288	TTCCCACCTGGAGAA[C/T]GTGTCAGAGGAAGAA	8850
rs756192781	snp	G/T	0.000132	0.00812297	intron-variant	KAT2B	GRCh38.p7	3:20119584	AACACCTTCTTCTCC[G/T]TTTGCCGGGGCAGTT	8850
rs756239469	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20073701	ACTGTCCTTGATTAT[A/C]ATTTACCTTTTTAAA	8850
rs756246510	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20117160	TCCAGCCACATTGTT[A/T]TCTGTCATAGTACAG	8850
rs756259279	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20091703	ATTTCCACTTCTGTT[G/T]GTCTTAAGATATTTT	8850
rs756277738	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20063818	AGTGCTGGGATTACA[A/G]ACGTGAGCCACCACG	8850
rs756292917	snp	A/G/T	0.000215264	0.0103728	intron-variant	KAT2B	GRCh38.p7	3:20072498	AAGTATAACGAGTTC[A/G/T]TTGTAGCGTGAGACT	8850
rs756296440	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20062863	AGTCCTTTGCCCATT[A/G]TAAAATTTCGTTGTT	8850
rs756327127	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20143263	TATTTTCTAGGGAGG[A/T]GAAGTTAATACACTA	8850
rs756361258	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20074422	GACCTCAGTTTTTTC[A/G]ACTCTGAAATGGGTT	8850
rs756414770	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20047218	GCGCACGTCACCATG[G/T]CCGGCTAATTTTTGT	8850
rs756425301	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20148625	GGGATTCCATGCACC[A/G]TGGCGGGTCAGTGAT	8850
rs756479878	snp	C/G	1.65644e-05	0.00287783	intron-variant	KAT2B	GRCh38.p7	3:20101480	CAAGGTAATCAGATG[C/G]AAGTTCTTTTCCTTT	8850
rs756532890	snp	C/T	1.64808e-05	0.00287057	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20125997	CGTGGTTGGCAATTC[C/T]CTCAACCAGAAACCA	8850
rs756565360	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20041694	GGGGGCGGGGACTTG[G/T]CCTTGTCAGCTCCTG	8850
rs756597188	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20095904	TGGGGACATGCCAGC[A/G]AGGAAGGTCAGTTAG	8850
rs756619045	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20123186	TCTGCGCCTCCCCAT[A/G]TGCTCTTTTTCTTTC	8850
rs756630580	snp	C/T	1.64925e-05	0.00287158	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20148264	GCCCAGAGACCCTGA[C/T]CAGCTTTACAGCACG	8850
rs756637093	in-del	-/A			intron-variant	KAT2B	GRCh38.p7	3:20085529	TTTTTTTTTTTTTGC[-/A]GGGGGCAGAGTCTTG	8850
rs756637853	snp	C/T	3.33294e-05	0.00408211	intron-variant	KAT2B	GRCh38.p7	3:20125886	TCTGTGTAATTTTTT[C/T]CTGTCTCTTGCATCT	8850
rs756737337	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20105588	TTGAGCCCAGCCTGG[A/G]CAACAGAATGAGACT	8850
rs756746276	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20041122	GAGTGGAGCGGTGCT[C/G]TCCATGTGGCGGGTG	8850
rs756747536	snp	A/G	1.6799e-05	0.00289814	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20122684	AGAAAAGAGGAAAAT[A/G]ACTGATTCTCATGTT	8850
rs756761837	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20078460	TTACTGCAACCTCCC[C/T]CTCTTGGGCTCAAGC	8850
rs756763799	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20078377	AGAGGTTTTTTGATT[A/G]TTTTTCAGTGTTGTC	8850
rs756765231	snp	A/G	4.9579e-05	0.00497866	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20122759	GGAATTAATCAACGA[A/G]GTTATGTCTACCATC	8850
rs756781413	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20080459	TTAGAGCTCTGTGGC[A/G]ATGTTCCTTCTTATA	8850
rs756787213	snp	C/T	5.00822e-05	0.00500386	intron-variant	KAT2B	GRCh38.p7	3:20146449	CGTATAGACCTTCTT[C/T]TAAAAGCGAAATTTT	8850
rs756872980	in-del	-/T			intron-variant	KAT2B	GRCh38.p7	3:20076951	ACAAAACATACTGGC[-/T]TATTGATTGAGATAG	8850
rs756957144	in-del	-/T	0.0553964	0.156938	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20137542	CCGTTCCTCCCTTCC[-/T]TTTTTTTTTTTGAGA	8850
rs756963775	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20077496	TGGCCACATGAAATG[C/T]GTTTACTCTGAATTG	8850
rs757023652	snp	C/T	1.65269e-05	0.00287457	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152414	CTTACAGCGAGTCTT[C/T]ACCAATTGCAAAGAG	8850
rs757031967	in-del	-/ATC	1.6654e-05	0.00288561	intron-variant	KAT2B	GRCh38.p7	3:20095255	TGTTTCTTTGATCTT[-/ATC]ATAAGCTGCTCATGT	8850
rs757041196	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20128638	CTGAATTGACAGAAA[C/G]AGCTCTCATCTATAC	8850
rs757065160	snp	C/T	5.54257e-05	0.00526401	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20136898	TTTGTAAAAATTTTT[C/T]TCCCCAGTCTAATGT	8850
rs757103731	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20116388	CCAGACTTTCATAGA[A/G]CCTTGAATATATCCT	8850
rs757123069	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20068712	TCAATAAATATTGTT[A/G]AAAGAATGAGTCAGT	8850
rs757125232	in-del	-/T			intron-variant	KAT2B	GRCh38.p7	3:20113493	CCCATAGTTCTGGCA[-/T]TGCTTATGCTAGGAG	8850
rs757133117	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20141416	AACTGGGGAGTACAC[A/G]AAGGCCATTTATTGA	8850
rs757135189	in-del	-/TG			intron-variant	KAT2B	GRCh38.p7	3:20081890	GCTCATATATATATA[-/TG]TATAAATGTATATAG	8850
rs757137681	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20072233	AGTCAGGGGTGAGGG[G/T]ATAGCTGTCATATAA	8850
rs757149853	snp	A/G/T	6.23012e-05	0.00558098	intron-variant	KAT2B	GRCh38.p7	3:20152301	GTTTAAAGGGAGTCA[A/G/T]AGATTGCTAATATTT	8850
rs757150190	snp	G/T			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20071159	ACATTGTTAATGATG[G/T]ATTTTATATTTTGCG	8850
rs757161045	snp	C/T	1.6582e-05	0.00287936	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20111629	CGTGCCACAGTTCTG[C/T]GACAGTCTACCTCGG	8850
rs757172805	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20044589	TCCTTTCACCTAGTC[A/G]GGGGTGAGGTGGGGT	8850
rs757180740	snp	C/G			utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20153058	TTTTAAAACACTCAT[C/G]TAGATGAGGTGCTTT	8850
rs757185835	in-del	-/TT			intron-variant	KAT2B	GRCh38.p7	3:20050488	ATTACCAGAGATTAG[-/TT]TTTTGTCTGTTCTTA	8850
rs757203322	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20122223	AATATGAAAATACAC[A/G]TTCTTTCCAAGAAGA	8850
rs757222683	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20087281	ATCTGATCACTGTAT[A/T]TTAAATGTATCAAAA	8850
rs757248757	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20110369	TCTTCACTTCTGGGA[A/G]ATAAAAAAAAAATAG	8850
rs757258616	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20053958	ATGTACCACCACACC[A/G]AGCTAATTTTTGTAT	8850
rs757285187	in-del	-/AT			intron-variant	KAT2B	GRCh38.p7	3:20078701	TATATGTGTATATAT[-/AT]GTATATATATATGTA	8850
rs757323568	in-del	-/TATT			intron-variant	KAT2B	GRCh38.p7	3:20045326	CCTGGCCTATTTATT[-/TATT]TATTTATTTATTTAT	8850
rs757336536	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20121204	TTTAGTAAATAATAT[A/G]TAATACTTCTGGAAG	8850
rs757338504	snp	A/G	5.03048e-05	0.00501496	intron-variant	KAT2B	GRCh38.p7	3:20095237	CAATTGAGGTCTTAC[A/G]TATGTTTCTTTGATC	8850
rs757349633	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20057906	GGAGGGCAGTTTCTT[A/G]TTCAACTCCAGCATA	8850
rs757369302	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20077726	GGTTTAGAATATTCT[A/C]GTTCATTCTCTGAAA	8850
rs757377789	snp	C/T	4.97277e-05	0.00498612	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20126023	AACCAAACAAGAAGA[C/T]CCTGATGTGGCTGGT	8850
rs757479044	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20127956	GCTCACTTGCCTGCC[A/C]CTCACCTCGTGCTGT	8850
rs757496555	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20103039	ATATATGCAATTTCA[G/T]TTATAAAGTATTTTC	8850
rs757506888	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20147647	TTTTACAGGGTGATC[A/T]GCCCAAAATTTGACT	8850
rs757532388	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20149631	AATGTTTCACATGAA[C/T]ATTTTATATATTTGT	8850
rs757535652	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20092703	TCTGTATCGTTTTTT[G/T]TTGTTGTTGTTGTTT	8850
rs757541428	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20100054	TTCCCTCCTCCATAC[C/T]CAGGTTAGAGATGTT	8850
rs757573083	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20144766	AAGGCATGCTGTAAG[A/T]ATAAAATCCTCTGAT	8850
rs757606591	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20073786	TGAATGGAGTTTAGG[A/G]TTGCCTCAGGAAATG	8850
rs757661549	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20072781	TCATTTTGGGGGTTG[A/G]GGCCTGAGGGTCTTT	8850
rs757698263	in-del	-/AGAT			intron-variant	KAT2B	GRCh38.p7	3:20109283	CTTCCCCTCAGCCCC[-/AGAT]AGATAGATAGATAGA	8850
rs757704987	snp	A/G	1.65179e-05	0.00287379	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20111643	GCGACAGTCTACCTC[A/G]GTACGAAACCACACA	8850
rs757718297	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20043387	GGGCCTAGGGATGAG[C/G]GCAGTGAACCAAAAT	8850
rs757748985	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20113974	ATAGCTTCACCACTC[C/T]GAACTATTTTTAGTG	8850
rs757770882	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20048109	TAAGTTTATTGCATA[C/G]AATTGTATCCTGTGG	8850
rs757787844	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20111868	AAGCCTGCATAAATA[A/G]CAAGATCGGAAATGA	8850
rs757831242	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20124192	TTAGCTGAGTTTAGG[C/T]TTTTTTCAGCTATAA	8850
rs757831683	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20138747	AAAATGTTTAGTTGT[A/G]CATTGATTTGTGAGA	8850
rs757846897	snp	A/G	1.75185e-05	0.00295955	intron-variant	KAT2B	GRCh38.p7	3:20101236	GTGTGGGTGTTCAGA[A/G]TTAGTATGATTGCAT	8850
rs757858323	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20057361	TATGTGGATGTGAGA[A/G]TCATCATCTCAGATA	8850
rs757860653	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20047269	GCCAACCTGGGTTTC[A/G]CCATGTTTAACAGGC	8850
rs757872004	snp	C/T	1.65037e-05	0.00287256	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20101357	AAACAATAGTTGAGT[C/T]GGCAAAAATGTTCCT	8850
rs757877323	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20096007	TAGGGGAAGAGACTC[C/T]GAGGCAGAGGGAGGA	8850
rs757893210	snp	A/C	1.66319e-05	0.00288369	intron-variant	KAT2B	GRCh38.p7	3:20127377	CCAAAAAGTATATTT[A/C]TATAACTAGGATAGG	8850
rs757901772	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20068647	AATGTAATCTCCAGG[A/T]GAGCAGAATCTTTGT	8850
rs757911346	snp	A/G	1.67607e-05	0.00289483	intron-variant	KAT2B	GRCh38.p7	3:20125855	TGTCCCATCCCCACT[A/G]TCTTGAGAGAATAGC	8850
rs757921307	snp	C/T			intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20137367	TTTGGTGGGTAGCAT[C/T]CTCTGTGAATGAGAA	8850
rs757946489	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20055994	ATTGCTGAGGAGTAT[G/T]CTGCTGTATGGACGT	8850
rs757949175	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20150855	ACTTCTTTGTGTCGT[C/G]TCATCCTTTTACTCC	8850
rs757973227	snp	C/G	1.65329e-05	0.0028751	missense, utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152440	AAGAGTACAACCCCC[C/G]TGAGAGTGAATACTA	8850
rs757995824	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20079763	GGACGTAAACATGGG[G/T]CCCAGCTAGCACAAT	8850
rs758013145	in-del	-/CTTC			intron-variant	KAT2B	GRCh38.p7	3:20130990	ATGTGAGAAACAGTT[-/CTTC]CTTCCTTTAGTTTCC	8850
rs758013667	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20108750	GCAGGAAGTGAGTGG[C/T]GGGCGAGTGAGCATT	8850
rs758109228	snp	A/G	1.65611e-05	0.00287755	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20122769	AACGAGGTTATGTCT[A/G]CCATCACGGACCCTG	8850
rs758121013	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20149656	ATTTGTAGTAATGAT[C/T]TCAGTAGCCTACACC	8850
rs758144002	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20091009	CTCCTACCTCAGCCT[C/T]CTGAAGTGCTGGGAT	8850
rs758154868	snp	C/G			downstream-variant-500B	KAT2B	GRCh38.p7	3:20154704	TTGTTTTTATACTTT[C/G]CATCTGTGAAATATA	8850
rs758155618	snp	C/T	1.69573e-05	0.00291177	intron-variant	KAT2B	GRCh38.p7	3:20140195	GGTGTATGGTGTTCA[C/T]ATGAATGAATTTACT	8850
rs758167989	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20078532	CATGCAGCAACATGC[C/T]CAGCTAATTTTTTTT	8850
rs758183214	in-del	-/C	1.66305e-05	0.00288357	intron-variant	KAT2B	GRCh38.p7	3:20146280	TGTATCCATAGACTT[-/C]TTTCCCTAAACACAT	8850
rs758186530	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20050649	TAAAAAATTAAAACA[C/T]TGCCAGCAATTTTCA	8850
rs758223038	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20128704	GGAACCAGAAAACAT[A/G]TCCTTAGAATGTTAT	8850
rs758249551	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20119154	AATCAAAAAAATACT[C/T]TTGTGGGGAGATATT	8850
rs758278000	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20060372	TTTGGGAGGCCAAGG[C/T]GGGCGGATCACCTGA	8850
rs758295068	snp	C/G	3.48712e-05	0.00417545	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20137075	TCTCACCACGCAACA[C/G]TGTTTTGTCACTCCT	8850
rs758317698	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20100297	TCCATTTGCTTGGCA[C/T]TGTCTGAGAAAGCCT	8850
rs758323367	in-del	-/TAAT			intron-variant	KAT2B	GRCh38.p7	3:20059032	CTAATTACATCAGCA[-/TAAT]TCAAACTGCTCATTT	8850
rs758342976	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20049143	GGGATTACAGGTGTG[A/C]GCCACCGCGCCTGGC	8850
rs758351272	snp	A/G	1.64925e-05	0.00287158	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152550	CCCTCTGCTTCTTAG[A/G]AACTCACCAAGCAGT	8850
rs758369735	snp	A/G			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070594	CAGGCGTGACCCACC[A/G]TGCCCGGCCTCTCTT	8850
rs758388012	in-del	-/T	7.44969e-05	0.0061027	intron-variant	KAT2B	GRCh38.p7	3:20099838	AAGTTTTTCTTTTTC[-/T]TTTTTTTAATGATTT	8850
rs758388907	snp	A/G	1.65222e-05	0.00287417	intron-variant	KAT2B	GRCh38.p7	3:20127564	GGTAAGGGTAAACCC[A/G]AGGTCTTAGAAGAAG	8850
rs758461474	snp	C/T			downstream-variant-500B	KAT2B	GRCh38.p7	3:20154756	CCGATTTTTAAACAT[C/T]TCCCATATGAGCTTC	8850
rs758526610	snp	C/T	1.64885e-05	0.00287123	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20111685	GAACATTGCTTCGCT[C/T]GGTCTTCACTGTTAT	8850
rs758527261	snp	C/G/T	4.94958e-05	0.00497452	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20111653	ACCTCGGTACGAAAC[C/G/T]ACACAGGTGTTTGGG	8850
rs758539445	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20069010	CTCTACAAAATCTTA[A/G]TGATACTTTTGTAGG	8850
rs758577764	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20044814	TGATTATTTGATGTG[C/T]ATTTAGAATCTTTGA	8850
rs758600308	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20107184	TACAGGCATGCGCCA[A/C]CACAGCTGGCTCATT	8850
rs758602233	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20083476	TAGAGTGAGGTTCAC[C/T]TGGGTGTTGACATGG	8850
rs758635666	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20093704	TTTAAATACGTATTT[C/T]AATCTTTCTTTAAAA	8850
rs758645515	in-del	-/G			intron-variant	KAT2B	GRCh38.p7	3:20095530	CCCTCAGAGTTTGCT[-/G]AACAATACGTTTCTT	8850
rs758645542	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20094682	ATGTTGAATGTCAAG[C/T]TAAAATAGGCCGTGG	8850
rs758731507	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20105259	TGTGGTTATAGAAAA[A/G]AATGTGGGCAAATAT	8850
rs758748350	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20077016	TGCCTCAGCCATATA[C/T]GTTCTTTGGAGCTGT	8850
rs758761296	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20133971	TTGTATTGATTCTAT[A/G]GAAGATATTTATGTA	8850
rs758794416	snp	A/C	3.29538e-05	0.00405904	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20072376	GGAAAAACCCTAACC[A/C]CTCACCCACTCCCCC	8850
rs758820026	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20065262	TTCCCCTCCCTGTGC[C/T]CAGGTTGCTAGCTGC	8850
rs758824446	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20128105	GTAGGGTTGTACCAA[A/G]GCTTTGTTGGACTTT	8850
rs758843305	snp	C/T	2.16055e-05	0.00328668	intron-variant	KAT2B	GRCh38.p7	3:20040832	TAGGGGCCCAGCCCG[C/T]GGGACCCCCCTCCCC	8850
rs758847449	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20132915	CTTGCATCGACATCC[A/G]TGTTAAAGTGAATTT	8850
rs758851292	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20147455	AGAGGCAACTTACTC[C/T]TATTTAGGGTGAGTT	8850
rs758881409	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20115974	TTAGGTGTAAATATA[A/G]CTAAATCCCTACAAA	8850
rs758921013	snp	A/C	1.64768e-05	0.00287021	missense, intron-variant, nc-transcript-variant	KAT2B	GRCh38.p7	3:20127450	CCTTGCTTTAATTAA[A/C]GATGGCCGTGTTATT	8850
rs758925186	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20112270	TCTTTGGAAACTAGA[C/T]TGCAAAAGCAGGGAT	8850
rs758925603	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20096085	ACAGCAAGGAGGGCA[A/G]CGTGGTGGAGCCCAG	8850
rs758938190	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20145963	TGAGTAGTGAATGCT[C/G]AGGGCTGCTTTCCTG	8850
rs758961236	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20127229	GGGAGTGCTGATGAC[A/G]TCTTGTGCAGGCGAC	8850
rs759038296	snp	C/T	1.67136e-05	0.00289076	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20111770	AAAACGAACTCTAAT[C/T]CTCACTCATTTCCCA	8850
rs759100700	snp	A/G	3.05984e-05	0.0039113	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20126103	TACATCACACGGCTC[A/G]TCTTTGACCCGTAAG	8850
rs759104393	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20082989	GTTGAATGCAGATCA[A/C]AACAGTAGGGGGTGC	8850
rs759129425	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20111307	TCAAAGTTATGCAGC[C/T]AGTTAAGTGACACAG	8850
rs759145421	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20084779	CAAGGGAATGGGATG[G/T]GTTCTTGAGCCTTCT	8850
rs759146278	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20043422	GAGAAGTTCAGAAAA[A/G]CTACTTTCTTGGAGT	8850
rs759170516	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20044207	AGATCTAGGCCAGGC[A/G]CAGTGGCTCAGACCT	8850
rs759214145	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20093161	ACTCTGAGACAAGGA[G/T]TTGAGTGCAAGTAGT	8850
rs759230001	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20094350	AACAGCATGGGGGAA[A/G]CTGCCTCCATGATCC	8850
rs759265729	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20133593	CATATTTGCTTATTT[C/G]TGGTAATTTTCTATC	8850
rs759297227	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20053643	TATATTCTAGAAGTC[C/T]GTATTATATTAGTAA	8850
rs759301611	snp	A/G	1.65274e-05	0.00287462	intron-variant	KAT2B	GRCh38.p7	3:20148347	TGCAAATATTTTGAA[A/G]TGATTTCCCACATGG	8850
rs759302009	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20103603	TTATAGAGATGGGGT[C/G]TCGCTGTGTTGCCCA	8850
rs759357568	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20132723	GAATCTGGAAAAGAT[A/T]TTTGGAGAGATGGCA	8850
rs759357702	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20146558	TGTGTTATCTCTAGT[C/T]TTTTAAGAAGGCAGC	8850
rs759358125	snp	C/T	1.7814e-05	0.00298441	intron-variant	KAT2B	GRCh38.p7	3:20122640	TTTAGAACCACCCAT[C/T]GTTTGCCTTTTATTT	8850
rs759358276	snp	C/G	4.96874e-05	0.0049841	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20146416	AGATTCCTATAGAAA[C/G]CATTCCTGGAATTAG	8850
rs759382998	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20052281	AATATTTGGAAATTA[C/T]GTTTTAAAAAATGAT	8850
rs759385124	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20065903	ATCCAATAGTAATAT[A/G]GAGGCCGCATGTATT	8850
rs759404912	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20095131	CTACAGGAGTTCAGA[A/C]ATTTTCTCTTATTAC	8850
rs759409572	snp	C/T	1.65299e-05	0.00287483	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20146329	AGATAATTAAAAAAC[C/T]GATTGAAAGAAAACA	8850
rs759446928	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20073440	TAGCATGGTGTTAGG[G/T]CGTCTGAAATTTTAT	8850
rs759494135	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20074316	GAGGTTTTATAATTT[A/T]GGACTAAATTATTGG	8850
rs759510956	snp	A/G	3.29772e-05	0.00406048	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20111686	AACATTGCTTCGCTC[A/G]GTCTTCACTGTTATG	8850
rs759511211	snp	A/G	3.64239e-05	0.00426739	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20040693	GGGAGGCGGTGGCTC[A/G]GCCCGAATCGCCGTG	8850
rs759511333	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20048685	TTTAGTTAGTCTGTC[A/G]TTAAGAGAAAAGTGG	8850
rs759516127	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20102550	CCTAACCATTTCTCT[A/G]TTGCTGGACATTCAA	8850
rs759546287	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20115481	AGTTTATATCTGGCC[A/C]TGGGGAAAGACAGGA	8850
rs759588937	snp	A/C	0.00145243	0.0269092	intron-variant, downstream-variant-500B	KAT2B, MIR3135A	GRCh38.p7	3:20137661	CCCACCTCAGCCTCC[A/C]AAGTAGCTGTGACTA	8850
rs759599161	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20047817	GACGGGGTTTCACCA[C/T]GTTGGCCAGGCTGGT	8850
rs759607666	in-del	-/AAAA			intron-variant	KAT2B	GRCh38.p7	3:20075264	GCGAGACTCTGTCTC[-/AAAA]AAAAAGAAAAAAGAA	8850
rs759619739	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20126344	ATATTTTACATTGCT[C/G]ATGACTCTCCTGTGC	8850
rs759620565	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20086900	CATTCTCCTGCCTCA[A/G]CCTCCCAAGTAGCTA	8850
rs759628939	snp	C/T			intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20136616	CATTCTGAAAACTTT[C/T]ATATTACTATTCAGC	8850
rs759643294	snp	C/T			intron-variant, downstream-variant-500B	KAT2B, MIR3135A	GRCh38.p7	3:20138043	TTGACTGCATATTAT[C/T]TTTAATAGTGATTTA	8850
rs759705157	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20110930	AAAAATGTACCTAGG[C/T]GACAAATGGTAGAAG	8850
rs759734783	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20151198	GATGTGATGACATAC[A/G]CTCTAACCAAGATAG	8850
rs759772034	in-del	-/ACT			intron-variant	KAT2B	GRCh38.p7	3:20064090	ATAAGAAGCTAGCAA[-/ACT]GTTTTCCAAGGTGGT	8850
rs759798473	snp	C/T	6.61244e-05	0.0057496	intron-variant	KAT2B	GRCh38.p7	3:20148235	TTGTTTCCCTTTTTC[C/T]TTTCAAGTAAAGAGC	8850
rs759807800	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20134459	TGGAGTGCGTTGGCG[C/T]GATCTCAGCTCAGAT	8850
rs759813724	snp	A/G	4.97393e-05	0.0049867	missense, utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152373	AAGAATAGGTACTAC[A/G]TGTCTAAGAAATTAT	8850
rs759821361	snp	C/T	3.29728e-05	0.00406021	stop-gained, nc-transcript-variant	KAT2B	GRCh38.p7	3:20101413	GAGGCACCATCTCAA[C/T]GAAGACTGCGATCTC	8850
rs759830094	snp	C/T	1.64958e-05	0.00287187	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20119680	AAACGCAGGGAGCAG[C/T]AGTCCTGCCTGCAAA	8850
rs759860880	snp	C/G			intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20136748	AAGGATTTTGATTTT[C/G]TTTTGGTTTTATAGC	8850
rs759879850	snp	C/T	1.65751e-05	0.00287876	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20101308	AATAACTTTGTGCAG[C/T]ACAAATTTAGTCACC	8850
rs759916188	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20068461	TCAAGTCTTTGCTCT[A/C]AGGTCATCTCAAAAA	8850
rs759916964	in-del	-/C	1.70804e-05	0.00292232	intron-variant, nc-transcript-variant	KAT2B	GRCh38.p7	3:20122828	GGTAAACCTGGGCAG[-/C]CAGCTGGTAGACCTC	8850
rs759923486	in-del	-/AG			intron-variant	KAT2B	GRCh38.p7	3:20099791	ACAGACAGAAACAGA[-/AG]AGAGAGGAGAGAGAG	8850
rs759945616	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20080398	GGAATTCTGCTTATC[C/G]TCCAAGGCTTGACTG	8850
rs759961036	snp	A/G	1.65078e-05	0.00287291	intron-variant	KAT2B	GRCh38.p7	3:20072479	GTTCCTAAATCTTCA[A/G]GGAAAGTATAACGAG	8850
rs760031254	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20079963	TTATGTCTCCCTGAC[A/G]TCCTCTGGTCATGAA	8850
rs760066743	snp	A/T	1.76971e-05	0.0029746	intron-variant	KAT2B	GRCh38.p7	3:20111824	TCTTTGTTTGATCCC[A/T]GAGCTTGAGGTTGCT	8850
rs760069006	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20050147	AGAGATTGCAGTGAG[A/C]TGAGATCATACCACT	8850
rs760091740	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20052110	CACTTTTCTCTGCCA[C/T]GTATCTCTGTATCTT	8850
rs760101922	snp	C/T	8.24178e-05	0.00641889	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20140322	GCTAAATCCACGGAT[C/T]CCGTACACAGAATTT	8850
rs760140894	snp	C/T	6.08057e-05	0.00551354	intron-variant	KAT2B	GRCh38.p7	3:20040823	GATGGGTGCTAGGGG[C/T]CCAGCCCGCGGGACC	8850
rs760142819	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20050095	GTCCCAGCTACTCAG[A/G]AGGCTGAGGTGGGAC	8850
rs760157279	snp	C/T	1.65091e-05	0.00287303	intron-variant	KAT2B	GRCh38.p7	3:20119576	AGTCATCTAACACCT[C/T]CTTCTCCTTTTGCCG	8850
rs760243684	in-del	-/ACAC			intron-variant	KAT2B	GRCh38.p7	3:20106440	CAACACCAGAAGTAC[-/ACAC]ACACACACACACACA	8850
rs760247699	snp	A/T	1.64885e-05	0.00287123	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20111699	TCGGTCTTCACTGTT[A/T]TGAGGCGACAACTCC	8850
rs760313273	in-del	-/AG	1.65345e-05	0.00287524	frameshift-variant, upstream-variant-2KB, nc-transcript-variant	KAT2B, MIR3135A	GRCh38.p7	3:20137019	CTTCCTCACATATGC[-/AG]ATGAATATGCAATTG	8850
rs760344503	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20083145	GGTTAAATTAGGGAG[C/T]GATACATCAAAGTTT	8850
rs760371103	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20054378	GTGATCCACCCTCAT[C/T]GGCCTTCCAAAGTGC	8850
rs760384379	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20084265	CAGACTGTCCACTCC[A/G]TCTACTTTCATTTGA	8850
rs760442086	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20045257	TCCTGGGCTCAAGCA[A/G]TCTGCCTGCCTCCAC	8850
rs760472826	in-del	-/TTTTTTTTTTTTTTT			intron-variant	KAT2B	GRCh38.p7	3:20063536	TCTGAGTAGGCCTCT[-/TTTTTTTTTTTTTTT]TTTTTTTTTTTTTTG	8850
rs760495333	snp	C/G	1.68043e-05	0.0028986	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20122799	GCAGCAATGCTTGGA[C/G]CAGAGGTCAGCAGGG	8850
rs760499367	snp	C/T	1.66588e-05	0.00288602	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20099902	GAGGAAAACCTGTGG[C/T]TGAAGGCTCTTTGGA	8850
rs760534103	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20107997	TATTTTTTAGTAGAG[A/G]TGGGGTTTCATCATG	8850
rs760571917	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20133773	GGAGAGAATAGTTCC[C/G]CCTACCATTGCTGGC	8850
rs760581446	snp	G/T	1.64746e-05	0.00287002	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20072341	TTTTTAGGCCGAGGA[G/T]TCTTGTAAATGTAAT	8850
rs760585703	snp	C/T	1.66026e-05	0.00288115	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20146429	AAGCATTCCTGGAAT[C/T]AGTACGTATAGACCT	8850
rs760656281	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20093305	GCAGGAATAATTGGG[A/G]GCTGGTGTAGAACAC	8850
rs760683584	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20105035	GGATTACAAGTGCGT[A/G]CCACCATGCCTGGCT	8850
rs760687116	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20065959	GTATTAGTTTCTTAG[A/G]CCTGTCATAACAAAT	8850
rs760693000	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20120457	GGTCTCAAACTCCTG[A/C]CCTCAGGTAATCTAC	8850
rs760694429	snp	C/G	1.65048e-05	0.00287265	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20119698	TCCTGCCTGCAAAGC[C/G]TCTTCTGGACTTGAG	8850
rs760713783	snp	A/C			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038766	AGAGTAACACTGGTA[A/C]CGTGAAGCACGTCAA	8850
rs760720849	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20146639	GGGAGCTTAGATGCC[C/G]CCTTGTAATAGCTGT	8850
rs760723794	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20149418	GGAGGATCACTTGAG[C/G]CTGGGAGTTTGAGGC	8850
rs760757315	snp	C/T	3.33122e-05	0.00408105	intron-variant	KAT2B	GRCh38.p7	3:20146267	GACTGACTTGAACTG[C/T]ATCCATAGACTTCTT	8850
rs760768270	in-del	-/TCTGGAG			intron-variant	KAT2B	GRCh38.p7	3:20115372	GGAAGACAGATGCCT[-/TCTGGAG]TCGCAGTGATCCCAG	8850
rs760775300	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20103975	ATGTAGTTTCTGACA[C/T]ACAGAGCAGGTGCTG	8850
rs760779027	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20126398	AATGTAACACTAAGA[C/T]GTTCTGCTTTCTTCA	8850
rs760832028	in-del	-/TG			intron-variant	KAT2B	GRCh38.p7	3:20142886	GGGTATCTATGTGCC[-/TG]TGTGTGTGTGTGTGT	8850
rs760850144	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20093712	CGTATTTTAATCTTT[A/C]TTTAAAAATCATTTC	8850
rs760862078	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20060804	AAATAAATTATCCAG[G/T]TGTAGAGGTACATGC	8850
rs760923919	snp	A/T	4.52458e-05	0.00475614	intron-variant	KAT2B	GRCh38.p7	3:20126122	TTGACCCGTAAGTGG[A/T]ACTTTCTGTTCCTTC	8850
rs760965921	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20113046	ACAACCTGATTGTCA[A/G]ATTTTTCTTTAGAGA	8850
rs760971345	snp	A/C	7.2767e-05	0.00603143	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20040669	TGCAGCGGGCACGGC[A/C]GAAGGACCGGGAGGC	8850
rs760985560	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20048033	ATATTGTCACAGCAA[A/G]GTACAAAGCATGGAG	8850
rs761019901	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20125427	ATTCCTTGAAGCCAG[A/G]GGTTGGCAAACTATA	8850
rs761033567	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20044691	CCTTCCTATAGAACT[C/T]AGATTCCTTGCCTTT	8850
rs761034062	snp	C/T	6.67011e-05	0.00577461	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152354	AACCATGAGTGAACG[C/T]CTCAAGAATAGGTAC	8850
rs761050687	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20097780	AGCCTCAAGTGATCT[C/G]CCCCCTCGGCCTTCC	8850
rs761069822	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20108420	TAAACCTTTCATTGC[A/G]GAAGATTGGACATAT	8850
rs761080858	in-del	-/ATATATA			intron-variant	KAT2B	GRCh38.p7	3:20062423	ATATTATATATTATT[-/ATATATA]ATATATAATATATAG	8850
rs761088774	in-del	-/G			intron-variant	KAT2B	GRCh38.p7	3:20066442	CTCACTCTGTCACCT[-/G]AGCTGGAGTGCAGTG	8850
rs761094668	snp	C/T	1.79371e-05	0.0029947	intron-variant	KAT2B	GRCh38.p7	3:20148512	TTAACATTTTCTAAG[C/T]ATAGATTTAAAACTC	8850
rs761096488	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20057222	CAACAAAGGGAATAG[C/G]GTAGTTGAAAAGGGA	8850
rs761104242	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20080494	TATAATTATATACCA[A/G]TCTGTACTGAACTGT	8850
rs761108091	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20138243	TTTTCCTCTCAGCTC[A/G]TACCTATGCTGTTAA	8850
rs761138879	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20109508	TTTTTGTAGAGATGG[A/G]CGTCTTACTATGTTG	8850
rs761141783	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20064297	GTGTAATGGCCAAAT[A/C]AGTGTAATTAGCATG	8850
rs761161509	in-del	-/T	0.42	0.183303	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152526	TTAATTGACAAGTGA[-/T]TTTTTTTCCCCTCTG	8850
rs761260398	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20120664	AAGAGTGTAGATACC[A/G]GGAGGGTAAAGAATT	8850
rs761297083	in-del	-/C	3.52871e-05	0.00420027	intron-variant	KAT2B	GRCh38.p7	3:20152323	CTAATATTTTTTTTT[-/C]CTGTGCAGATCTGAA	8850
rs761338234	in-del	-/A			intron-variant	KAT2B	GRCh38.p7	3:20139174	CTGCCTCAGTCTCCC[-/A]AAAGTGCTGAGATTA	8850
rs761342906	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20079562	AACAATCACACTAGA[G/T]CTTACTTCTTGAGTA	8850
rs761350216	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20132283	GAGGCTGAGGCAGGA[C/G]AATCACTTGAACCCA	8850
rs761352188	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20119779	TCCAGGAGCTCCATT[A/G]CCTGAGGAGTGCAAA	8850
rs761392475	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20061474	GACTTCCTACTTTCA[A/G]TTCTTTTGGGTATAT	8850
rs761459475	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20063278	TTGTTTGTTGCTCAG[G/T]CTGGTCTTGAACTCC	8850
rs761460614	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20144040	CAATAAATTAAAAAA[G/T]ATCTCTTCTCCATAC	8850
rs761504640	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20143604	TCATTGCAGCGCTAT[C/T]CACAATAACAAAGAC	8850
rs761506826	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20046453	CGGGCATGATGGTGC[A/G]TGCCTGTAGTCCCTA	8850
rs761510735	snp	A/G	6.59196e-05	0.00574068	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20072373	GCTGGAAAAACCCTA[A/G]CCCCTCACCCACTCC	8850
rs761537683	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20123605	AAAACCGTATTTAAA[C/T]TTCCCATATAGCCAG	8850
rs761538578	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20113357	ACTCCTCCCTTCCCA[A/G]CACCTGTTATGGTAT	8850
rs761543745	in-del	-/CT			intron-variant	KAT2B	GRCh38.p7	3:20040842	GCCCGCGGGACCCCC[-/CT]CCCCCTCCCGCTTCC	8850
rs761593639	snp	C/T	1.7324e-05	0.00294307	intron-variant	KAT2B	GRCh38.p7	3:20114832	TAATTAGGGCTGTTA[C/T]CCTTACAGTAGTTTT	8850
rs761597101	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20055425	AGTGGTAAGTGCCTC[A/G]CAGAGAATGAAAACA	8850
rs761624829	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20112688	TGGCTAGGTATGATA[C/T]AGCCTTCCTTCCCCA	8850
rs761625144	snp	A/G	1.64871e-05	0.00287111	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20101423	CTCAACGAAGACTGC[A/G]ATCTCCCAATGATGA	8850
rs761629718	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20112852	TTTGTCTCAGTGAAG[A/G]TAGAGTTTTAATTCA	8850
rs761633377	snp	G/T	1.71097e-05	0.00292481	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152543	TTTTTTCCCCTCTGC[G/T]TCTTAGAAACTCACC	8850
rs761735374	in-del	-/TTTTTTTTTTTTT			intron-variant	KAT2B	GRCh38.p7	3:20144279	TGCCCTTGGGATTCT[-/TTTTTTTTTTTTT]TTTTTTTTTTTTTTT	8850
rs761748890	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20089689	CCCAGTGTGAGCCAC[C/T]GCGCCTGGCCTACTT	8850
rs761802592	snp	A/G	1.67346e-05	0.00289258	intron-variant	KAT2B	GRCh38.p7	3:20148201	GCTGGCAATAGGGTA[A/G]AACTCTAATCATTGC	8850
rs761822849	snp	C/T			intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20136917	CCAGTCTAATGTATT[C/T]GTTTGTATACTAACT	8850
rs761838031	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20105105	TGGCCAGGCTAGTCT[C/T]GAACTCCTGACCTCA	8850
rs761839145	snp	A/C	2.04234e-05	0.00319551	intron-variant	KAT2B	GRCh38.p7	3:20095421	AAGGTGAGATTTTAA[A/C]ATTTTAAAAACATTT	8850
rs761841676	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20054579	TTCCATGCCATCCTA[A/G]TCAGTCCCCATGCGT	8850
rs761842920	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20083371	CTTCTTAATAAAAGG[C/T]TAAGAGAAGGGTTTC	8850
rs761868414	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20135100	CTTCCCCATTTTACT[A/G]TCGTCTCCTCAAGGA	8850
rs761878043	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20059488	TTTGGGAGGCCGAGG[C/T]AGGTGGATCACGAGG	8850
rs761889092	snp	A/T			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038942	ACTCCCCCACCTCCC[A/T]ATGTTTATATATTAA	8850
rs761898798	in-del	-/CATTGCCTTG			intron-variant	KAT2B	GRCh38.p7	3:20123877	ATGCTGCTGTCATCT[-/CATTGCCTTG]CATCTGAGGGCATGC	8850
rs761904977	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20105930	CTATTGCCATGTATA[C/T]TGAGCATTCATTATT	8850
rs761915404	snp	G/T	3.30901e-05	0.00406743	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20122732	ACCCCGAGTTATGGG[G/T]GATATTCCGATGGAA	8850
rs761921756	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20151052	GAGAACATTTTGATC[C/T]GTTCAGTCACACTTG	8850
rs761927918	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20116638	CCCCTTTTTTTCTGT[A/G]TGTCTTTTCATCTCC	8850
rs761932837	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20094514	CCGCATGGGATTGGG[G/T]ATTAAATGTAATAAC	8850
rs761949828	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20077894	TAAAAAGCAGCTTGG[A/G]TCTTGCATGGTGGCT	8850
rs762001355	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20117552	GAAAAAAACATAGAG[A/C]CTGGCACTTTAGTAT	8850
rs762012041	snp	C/G	1.66286e-05	0.0028834	intron-variant	KAT2B	GRCh38.p7	3:20146286	CATAGACTTCTTTCC[C/G]TAAACACATTTCCTT	8850
rs762039418	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20076692	TTGCCAGAGTATTTT[A/G]GCAAGTTTCCTACAT	8850
rs762079689	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20147139	GTTCTTTTTAGTATA[C/T]TTAAGCTTTAATAAA	8850
rs762133394	snp	C/G			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038340	AAATTTTCAAACATA[C/G]AGAAAAGTTGAAAGA	8850
rs762163690	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20049535	TGCACCATTTTGCCT[C/G]CTCTTCCAAAACTTT	8850
rs762207314	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20047668	GCTGGAGTGGAGTGC[A/G]GTGGTGTGATCTCAG	8850
rs762223190	snp	A/G/T	3.30514e-05	0.00406507	synonymous-codon, missense, upstream-variant-2KB, nc-transcript-variant	KAT2B, MIR3135A	GRCh38.p7	3:20136977	GAATCATTTGAAAGA[A/G/T]TATCACATAAAGCAT	8850
rs762224379	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20097925	GTTACATATTTTAGT[A/G]GAATTAAAAAATTTC	8850
rs762227355	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20095594	TTGAACACATCATTC[C/T]CTTTGAGGCTTTTAC	8850
rs762240111	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20086982	AGATGGGGTTTCACC[A/G]TGTTGGCCAGGCTGC	8850
rs762269482	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20043862	TTGCTCTACCTTTGC[A/C]ACAGGCCCCTTGGCA	8850
rs762269902	snp	C/T	1.64751e-05	0.00287007	missense, intron-variant, nc-transcript-variant	KAT2B	GRCh38.p7	3:20127487	ATCTGTTTCCGTATG[C/T]TCCCATCTCAAGGAT	8850
rs762298110	snp	C/G			missense, utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152399	ATTATTCATGGCAGA[C/G]TTACAGCGAGTCTTT	8850
rs762340800	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20081747	GAGGAAAGATTGTAA[A/G]AACACTTTTAATTTG	8850
rs762343587	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20058794	AACCATTTAATCTGT[A/G]TATGAAAAGCTAAAG	8850
rs762403927	snp	C/T	0.000148514	0.00861596	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20125927	TTCTGTCAGCACACT[C/T]GGCCAGGGATGAGGC	8850
rs762406692	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20111209	ATTTCATTTAATGCT[C/T]ACAAGAACCCAATGA	8850
rs762438108	in-del	-/C			intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20135653	AGCAAGACTCCATCT[-/C]AAAAAAAAAAAAATA	8850
rs762459103	snp	C/T	1.66015e-05	0.00288105	intron-variant	KAT2B	GRCh38.p7	3:20148221	CTAATCATTGCTCCT[C/T]GTTTCCCTTTTTCCT	8850
rs762472149	in-del	-/TCT			intron-variant	KAT2B	GRCh38.p7	3:20104530	TCTCACTGATACTGA[-/TCT]TCTCAAAAATGGGTA	8850
rs762487887	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20104579	GCACCAGCAGGCTTT[A/T]TCTTGATGTTGCTGT	8850
rs762513968	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20043264	AGGGTTACCAACTGG[C/G]TGTCAGGCATTGGGC	8850
rs762573361	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20131089	GGCGTGATCTCGGCT[C/G]ACTGCAAACTCCGCC	8850
rs762607505	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20052137	TCTTGTTCTCAAAGC[C/G]TCATTCCAGTCTGTT	8850
rs762663547	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20143770	ATTATCCTAAGCAGA[C/T]TAACACAGGAACAGA	8850
rs762702192	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20093136	TTAGTTTGAGTTCCC[C/T]AAGAAACAGACTCTG	8850
rs762725222	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20064480	GTTAGAGAGATCTTA[C/T]TGGGTGAGAAGTTAC	8850
rs762726271	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20079148	TCAGGTGATCCACCC[A/G]CCTCGGCCTCTCAAA	8850
rs762728649	snp	A/G	3.34762e-05	0.00409108	intron-variant	KAT2B	GRCh38.p7	3:20146457	CCTTCTTTTAAAAGC[A/G]AAATTTTTTAGTAAT	8850
rs762742633	snp	A/G	0.000123054	0.00784296	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20040688	GGACCGGGAGGCGGT[A/G]GCTCGGCCCGAATCG	8850
rs762789728	snp	C/T	1.65296e-05	0.00287481	intron-variant	KAT2B	GRCh38.p7	3:20140374	AAGGAGGTAAGCAGG[C/T]GGTTGACTCCCTTAC	8850
rs762820176	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20075003	GGGCGTGGTGGCTCA[C/T]GCCTGTAATTCCAGC	8850
rs762823707	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20047705	GCAGCCTCCACCTCC[C/T]GGGTTCAAGCAATTT	8850
rs762835780	snp	C/T	1.6489e-05	0.00287128	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20101436	GCGATCTCCCAATGA[C/T]GATATTTCTGGATAC	8850
rs762909661	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20074028	TTTGTTTCCTTTTTT[A/G]TTTCTTACCAAGCTT	8850
rs762912165	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20046907	TGGCAACTAGTGAGT[A/G]GAGGCCAGTAATGTT	8850
rs762920270	snp	C/G	2.73288e-05	0.00369643	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20126095	CAAAAGAATACATCA[C/G]ACGGCTCGTCTTTGA	8850
rs762933079	snp	G/T	1.72116e-05	0.00293351	intron-variant	KAT2B	GRCh38.p7	3:20111575	TGGGATATTGATGGT[G/T]CTTGACTTCTCTTGT	8850
rs762935449	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20113489	CTCAGCCCATAGTTC[G/T]GGCATGCTTATGCTA	8850
rs762961759	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20085309	GCCTGTTTCCCAAAG[G/T]CTTCAGATTGACCTC	8850
rs762993932	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20041046	AGCTTCGGCATCCGA[C/G]CTCCCGGGCTACCTT	8850
rs762995811	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20095538	GTTTGCTGAACAATA[C/T]GTTTCTTCATGACTG	8850
rs763002342	snp	G/T	1.66048e-05	0.00288134	missense, utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152366	ACGCCTCAAGAATAG[G/T]TACTACGTGTCTAAG	8850
rs763031394	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20123735	CAACTCCCCAGCCTT[C/G]TTTTGGTCTTTTGCA	8850
rs763049785	snp	C/T	3.39282e-05	0.00411861	intron-variant	KAT2B	GRCh38.p7	3:20101275	GAAGAAATTGCCTTC[C/T]CTCTTTTTAAGGGTG	8850
rs763051895	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20096271	CTGCCATTCCCCGTA[G/T]CTGCCTCTTCACTAG	8850
rs763062001	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20063922	TAAGGGTCCAGCTTC[A/C]TTCTTGTGCACACAG	8850
rs763084224	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20134140	CAGTCTTTTACTTCA[G/T]GCTTTTGCATTTTAT	8850
rs763114490	in-del	-/A			downstream-variant-500B	KAT2B	GRCh38.p7	3:20154887	ACCAACTGAGAAGTT[-/A]AAAAAAAAAAAAAAA	8850
rs763135714	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20132398	AAATATTGAATTTGA[C/T]ATTATATACAGCTTT	8850
rs763185872	snp	A/G	1.65381e-05	0.00287555	intron-variant	KAT2B	GRCh38.p7	3:20119549	CGTTTCTTGTTACCT[A/G]AGAAAGGAGTCAGTC	8850
rs763234716	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20117620	AAGTGCTATGGGTTG[A/G]TATCTCTCTTGCTTG	8850
rs763242464	snp	A/G	0.00128617	0.0253265	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20137559	TTTTTTTTTTGAGAC[A/G]GGGTCTCACTTTGGT	8850
rs763307456	snp	C/T	1.65258e-05	0.00287448	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20122752	TTCCGATGGAATTAA[C/T]CAACGAGGTTATGTC	8850
rs763309541	snp	A/T			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039736	ACTTTTCAAAAATAT[A/T]TTTTTTTTCCTCTGG	8850
rs763313076	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20048199	CATTTGGCAGGCACA[A/G]TACAAAAAGCCTGAG	8850
rs763340511	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20116822	ATAGAAGCTCAGGGA[A/G]GAGCAACAAATTGCC	8850
rs763347357	in-del	-/TTTTC			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20069515	GAGCTTTTCTTTTTC[-/TTTTC]TTTTCTTTTCTTTTT	8850
rs763396420	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20129152	AATAGAAATATAAAG[C/T]AGCCTGCAAATATGA	8850
rs763397741	snp	C/T			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20069786	CACCCGCCTTGGCCT[C/T]CCAAAGTGCTGGAAT	8850
rs763417546	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20128179	AAGTGTAGTCGATAG[C/G]AAATGAAGGGATATT	8850
rs763450728	in-del	-/TAC			intron-variant	KAT2B	GRCh38.p7	3:20120366	CTGAGTAGCTGGGAT[-/TAC]AGGTGCCCACCATCA	8850
rs763471342	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20089864	TAGTATACAGAAACA[C/T]GGCTGGGCATGGTTA	8850
rs763487969	snp	C/T	2.59595e-05	0.00360265	intron-variant	KAT2B	GRCh38.p7	3:20095442	AAAAACATTTTCTCT[C/T]ATTATTCAAATGTAC	8850
rs763539616	snp	A/C	4.14748e-05	0.00455365	intron-variant	KAT2B	GRCh38.p7	3:20040826	GGGTGCTAGGGGCCC[A/C]GCCCGCGGGACCCCC	8850
rs763548402	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20050249	CCAGTTTATATAAGA[C/T]GGTTCACACAACAGT	8850
rs763559145	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20088723	TTGATTGTTTCTTTT[C/G]CTATATAGAAGCTTT	8850
rs763576818	snp	C/T	1.65201e-05	0.00287398	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20146363	ACAAATTCGAAAAGT[C/T]TACCCTGGACTTTCA	8850
rs763586082	snp	A/G	1.65162e-05	0.00287365	missense, upstream-variant-2KB, nc-transcript-variant	KAT2B, MIR3135A	GRCh38.p7	3:20137003	AGCATGACATCCTGA[A/G]CTTCCTCACATATGC	8850
rs763589872	snp	A/C	3.29832e-05	0.00406085	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20111724	AACTCCTGGAACAAG[A/C]AAGACAGGAAAAAGA	8850
rs763631131	in-del	-/TT	1.78267e-05	0.00298547	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20137090	CTGTTTTGTCACTCC[-/TT]TTCTTAATATGTTCT	8850
rs763639026	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20118616	TAATCTCAGCTACTC[A/G]GGAGGCTGAGGCAGG	8850
rs763660261	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20050278	GTATCTCAACATGAT[A/G]AAAAGGAGTCATTAA	8850
rs763665386	in-del	-/AGT	1.6522e-05	0.00287414	intron-variant	KAT2B	GRCh38.p7	3:20072492	AAGGAAAGTATAACG[-/AGT]AGTTCATTGTAGCGT	8850
rs763704129	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20040928	GGAAGTGCTCTTGTC[C/G]CCCGCGCCCAATTAG	8850
rs763776765	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20142234	TTTTTAGAAGCCAAG[G/T]CTCCCTCCCCATTCT	8850
rs763828284	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20082786	AACCAAAAATCCCTC[C/T]CCACCAAATACGTAA	8850
rs763841855	snp	A/G	1.69473e-05	0.0029109	intron-variant, nc-transcript-variant	KAT2B	GRCh38.p7	3:20122812	GACCAGAGGTCAGCA[A/G]GGTAAACCTGGGCAG	8850
rs763859890	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20141252	CCTTCTAGGTATTAA[G/T]TGATTTGTTATCTGG	8850
rs763865060	snp	C/T			intron-variant, nc-transcript-variant	KAT2B	GRCh38.p7	3:20122829	GTAAACCTGGGCAGC[C/T]AGCTGGTAGACCTCT	8850
rs763893962	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20087208	ATGGATGATACCGAG[G/T]GTTTCCAACACAAAG	8850
rs763900256	in-del	-/GAAAT			intron-variant	KAT2B	GRCh38.p7	3:20076908	AGTAATTGTACACAC[-/GAAAT]GAAATATTCTTGAAT	8850
rs763903349	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20082278	GACCTCAAATGATCC[A/G]CCCTCCTCAGCCTCC	8850
rs763927504	in-del	-/AG			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039786	AGTTGTCTCTCTGTC[-/AG]AGACAGGGTGGAAGA	8850
rs763931751	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20053924	TGCCTCAGTCTCCCA[A/G]GTAGCTGAGATTACA	8850
rs763941376	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20045258	CCTGGGCTCAAGCAA[C/T]CTGCCTGCCTCCACC	8850
rs763947759	snp	G/T			downstream-variant-500B	KAT2B	GRCh38.p7	3:20154419	ATCTTGTGGTGTGTT[G/T]TATTCATTCAGTAGG	8850
rs763980181	snp	A/G	3.30989e-05	0.00406797	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20101317	GTGCAGTACAAATTT[A/G]GTCACCTGCCAGCAA	8850
rs764031294	snp	C/T	1.66524e-05	0.00288547	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20099910	CCTGTGGTTGAAGGC[C/T]CTTTGGAAAAGAAAC	8850
rs764088579	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20094500	ATTACTAATACCGAC[C/T]GCATGGGATTGGGGA	8850
rs764125658	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20106740	GGATTTTATGATAAT[A/T]TTTATAACCTATCAT	8850
rs764159478	snp	C/G	1.68125e-05	0.00289931	intron-variant	KAT2B	GRCh38.p7	3:20095229	TTGGTTTCCAATTGA[C/G]GTCTTACATATGTTT	8850
rs764179147	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20052632	ATCCAGCCTAGGCTA[C/T]GGAGAGAGACCCCAT	8850
rs764184705	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20105064	CTAATTTTTGTATTT[G/T]TAGTAAAGATGGGGT	8850
rs764194304	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20076540	GTGCTTTTTGAAAAA[C/T]TTTTTTTCTTAATGG	8850
rs764226308	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20132847	TATGGATGAAGGGTA[C/G]AAATTTATAGTTTCT	8850
rs764228915	in-del	-/TTTTCTTTTC			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20069510	GCAGAGAGCTTTTCT[-/TTTTCTTTTC]TTTTCTTTTCTTTTT	8850
rs764232813	snp	A/G	1.70446e-05	0.00291925	intron-variant	KAT2B	GRCh38.p7	3:20140185	GTAGATATTTGGTGT[A/G]TGGTGTTCATATGAA	8850
rs764248330	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20149526	AAAAAAAAAATTGTG[A/G]AAGTGTTAAAAATGT	8850
rs764248956	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20094400	CCTCCCTTGACATGT[C/G]GGGATTGCAATTTGA	8850
rs764259517	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20114621	AGATTAATGCATTTC[C/T]ACTGATGTAATTCAT	8850
rs764269194	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20064962	TTCACACCCATCTCA[C/T]TCATTAACACTGCGT	8850
rs764270572	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20104119	AATTATTTGAATATC[A/G]CTTTAGAAATTAAGA	8850
rs764314693	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20048054	AAGCATGGAGGGAGG[A/T]GGATAAGATGTTGTT	8850
rs764317165	in-del	-/AG			intron-variant	KAT2B	GRCh38.p7	3:20072803	AGGGTCTTTGACCTC[-/AG]GGTTGAAACCTCAAC	8850
rs764326189	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20115668	TACTCTTTTTACTGT[A/G]CTGTGTTTTGACAAA	8850
rs764334568	snp	A/T	1.64977e-05	0.00287203	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20140349	ATTTTCTGTCATCAT[A/T]AAAAAGCAGAAGGAG	8850
rs764363246	in-del	-/AC			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039538	TTTCAAACAAAAATT[-/AC]ACAGAGAATAGTAAG	8850
rs764381505	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20048773	GTCATCTGATTCAAA[C/T]GGGGAATTAGAACAG	8850
rs764403827	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20115231	AGTTACCACCAGGTA[C/T]AATGGTGGATAGTGA	8850
rs764428528	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20126483	GTGGGCAATTATTGG[A/G]ATATAAGACAGGTTA	8850
rs764430238	in-del	-/T			intron-variant	KAT2B	GRCh38.p7	3:20096899	ATTATATTTTTAAAA[-/T]TTGGTAGATATTAAA	8850
rs764433031	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20066443	CTCACTCTGTCACCT[A/G]GCTGGAGTGCAGTGG	8850
rs764448971	in-del	-/ATT			intron-variant	KAT2B	GRCh38.p7	3:20129974	CCATTTTTTAAAATT[-/ATT]ATTATTATTATTATT	8850
rs764508390	snp	C/T	1.65403e-05	0.00287574	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20111635	ACAGTTCTGCGACAG[C/T]CTACCTCGGTACGAA	8850
rs764538271	snp	C/T	3.29495e-05	0.00405877	missense, intron-variant, nc-transcript-variant	KAT2B	GRCh38.p7	3:20127481	GGTGGTATCTGTTTC[C/T]GTATGTTCCCATCTC	8850
rs764543611	in-del	-/TTTT			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20069520	TTTCTTTTTCTTTTC[-/TTTT]CTTTTCTTTTTTTTT	8850
rs764591571	snp	C/G	3.48195e-05	0.00417236	intron-variant	KAT2B	GRCh38.p7	3:20126134	TGGTACTTTCTGTTC[C/G]TTCTTCCTTATTTCC	8850
rs764622394	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20097014	TGAACAGCTGGATTC[C/T]CCACAGCCATTAGCA	8850
rs764646719	snp	C/T	1.65704e-05	0.00287836	intron-variant	KAT2B	GRCh38.p7	3:20148367	TTCCCACATGGAATT[C/T]CCATATTAGATACCT	8850
rs764651046	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20111418	GACACAAGTGGTGAT[A/G]TAAGGGTAATCTAAT	8850
rs764684238	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20042393	GAACAGGACACCGAC[C/T]GTAGTAGGCAGAAGG	8850
rs764694634	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20150676	CAGAGGAAGAAGAAT[C/G]CTATCTATAGCTTTA	8850
rs764742214	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20080502	TATACCAATCTGTAC[C/T]GAACTGTGATTAAGA	8850
rs764763522	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20090903	TGACACCACACCTGC[C/G]TAATTTTTATTTATT	8850
rs764817661	snp	G/T	1.67237e-05	0.00289164	intron-variant	KAT2B	GRCh38.p7	3:20146455	GACCTTCTTTTAAAA[G/T]CGAAATTTTTTAGTA	8850
rs764828592	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20119799	AGGAGTGCAAAAGGT[A/G]GACTTGAACCAAGTA	8850
rs764916630	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20130667	GTCTTATTACTTCCC[A/G]GAAAGGCAATTCCCC	8850
rs764918638	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20118003	AATCCTGTGTATTTT[A/G]TATGCTTTACCTGGT	8850
rs764920595	snp	A/C	1.64798e-05	0.00287047	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20072374	CTGGAAAAACCCTAA[A/C]CCCTCACCCACTCCC	8850
rs764956009	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20142407	GTATTTTTTTCCACA[G/T]AATTCAGTTGATTTT	8850
rs765005938	in-del	-/T	0.42	0.183303	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152525	TTAATTGACAAGTGA[-/T]TTTTTTTTCCCCTCT	8850
rs765007593	snp	C/G	1.71528e-05	0.0029285	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152545	TTTTCCCCTCTGCTT[C/G]TTAGAAACTCACCAA	8850
rs765012634	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20071833	AGTGTGCCTTCAGCT[C/G]GGTGTGCCCCGTCTC	8850
rs765020319	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20061510	GAAGTGGAATTGCTG[C/T]GTCATATAGTAATTC	8850
rs765021156	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20113360	CCTCCCTTCCCAACA[C/T]CTGTTATGGTATTTA	8850
rs765021821	snp	A/T	1.65061e-05	0.00287277	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20125924	ATTTTCTGTCAGCAC[A/T]CTCGGCCAGGGATGA	8850
rs765032548	in-del	-/G			intron-variant	KAT2B	GRCh38.p7	3:20042543	TCCACAAAAACCTAT[-/G]GAAAAAAAAGAGCAA	8850
rs765044482	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20144200	GTCCCTTGGTGAAGA[C/G]AAGGAAACTTTCAAA	8850
rs765050894	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20142660	TGACTCCAAGGGAAA[A/G]GTAGGATCTGTAGGG	8850
rs765060330	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20072248	GATAGCTGTCATATA[A/C]TTAGTGTACATTGTT	8850
rs765086965	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20045643	AACCCATTGACTAAC[C/T]CTTCCTAAAGGAGCA	8850
rs765111212	snp	A/G			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039878	CGGATGGGGGGCCGC[A/G]GAGGGGGGAGGTGGC	8850
rs765138297	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20123020	GTCCACTTACTAATA[A/T]TCTCACAGTTGAAGG	8850
rs765159204	snp	A/G	4.95397e-05	0.00497668	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20101342	CAGCAAAAGAAAGGC[A/G]AACAATAGTTGAGTT	8850
rs765199450	snp	C/G	1.67753e-05	0.00289609	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20099867	TTCTTTGCAGCTCTT[C/G]AGAAAGTCTATTTTA	8850
rs765247811	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20084331	AACCTTTCTCATACA[A/G]TATTCTCCTGCTTCA	8850
rs765251940	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20054581	CCATGCCATCCTAAT[C/G]AGTCCCCATGCGTTG	8850
rs765295902	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20107121	CACTGCAACCTCCAC[C/T]TCCTGGGTTCAAGCC	8850
rs765305736	snp	A/C	5.00188e-05	0.00500069	intron-variant	KAT2B	GRCh38.p7	3:20095252	ATATGTTTCTTTGAT[A/C]TTATCATAAGCTGCT	8850
rs765335654	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20083379	TAAAAGGTTAAGAGA[A/G]GGGTTTCTTTTAATA	8850
rs765338229	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20067162	AAAATATACTTTGTA[C/T]TGGGATCCCAAGACT	8850
rs765360282	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20059493	GAGGCCGAGGCAGGT[A/G]GATCACGAGGTCAGG	8850
rs765415523	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20057911	GCAGTTTCTTATTCA[A/G]CTCCAGCATAAACAC	8850
rs765456046	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20076751	TTCTTAATTGTTACC[A/G]ACAAAGTACAAGTTG	8850
rs765501786	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20148780	GCTGGCACTTTAGAT[A/G]TAACTTTGCTTATAT	8850
rs765545370	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20116685	TGATGGTCAGAGACC[C/T]AGTTTTGTCACAATA	8850
rs765573715	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20128068	GTGTGTGAGGAGAGT[A/G]AGTGGTTTCACCTAC	8850
rs765587521	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20147339	TGCCTACTTGTGCCA[C/T]GCATTTATCTGTTTT	8850
rs765627638	snp	A/C/T	8.52649e-05	0.00652887	intron-variant	KAT2B	GRCh38.p7	3:20040828	GTGCTAGGGGCCCAG[A/C/T]CCGCGGGACCCCCCT	8850
rs765651555	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20049559	AAACTTTCGCATGGG[A/G]TAGAGGGGGTCGCTT	8850
rs765653646	snp	A/C			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038360	AAGTTGAAAGAATTG[A/C]GCACTGTGCCCATTA	8850
rs765665727	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20126979	AAGGATTCCATAATG[C/T]GGAATTTTGCAAATT	8850
rs765679129	snp	G/T	1.83906e-05	0.00303232	intron-variant	KAT2B	GRCh38.p7	3:20148532	ATTTAAAACTCTGGA[G/T]GGCGGTGTGGGGGAC	8850
rs765688747	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20114843	GTTATCCTTACAGTA[G/T]TTTTTTTTTAATCTT	8850
rs765741738	snp	A/G	1.66302e-05	0.00288355	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20111762	CCTCTTGAAAAACGA[A/G]CTCTAATCCTCACTC	8850
rs765743656	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20048914	TCTTGCTCTGTCGCC[A/G]GGCTGGAGTGCAGTG	8850
rs765748742	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20057449	TATTTTGCTCATCCT[C/G]GTTGATTTGGTGCCA	8850
rs765749090	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20065092	ATACTATAACAACAT[C/G]GGTTGCATACTATTG	8850
rs765768113	in-del	-/TA			intron-variant	KAT2B	GRCh38.p7	3:20099310	TCTGCAGACTTTCTT[-/TA]CCTAAAGAGCCTGTG	8850
rs765768640	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20058797	CATTTAATCTGTATA[C/T]GAAAAGCTAAAGTTA	8850
rs765803113	snp	C/T	1.64765e-05	0.00287019	missense, intron-variant, nc-transcript-variant	KAT2B	GRCh38.p7	3:20127515	GATTCACAGAGATTG[C/T]CTTCTGTGCTGTAAC	8850
rs765836560	snp	A/T			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20069469	CTTTAAGAATTTATG[A/T]CCTGCTTCTGGGGAT	8850
rs765867291	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20151594	ATTCCTTAAATTAGT[C/T]CTGACAGTGAGGATT	8850
rs765885080	snp	A/G			missense, utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152431	CCAATTGCAAAGAGT[A/G]CAACCCCCCTGAGAG	8850
rs765891305	in-del	-/AG			intron-variant	KAT2B	GRCh38.p7	3:20084005	GTATTTGTTGAGAAC[-/AG]AAAGTTCAGCGCTAC	8850
rs765898446	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20139955	CTAATTTTTACTTAA[C/T]ACCTGTTTCTGTTTT	8850
rs765904687	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20097936	TAGTAGAATTAAAAA[A/G]TTTCAGTCTTAGTCT	8850
rs765907257	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20081766	ACTTTTAATTTGCAA[A/G]TAATTAAAAATTTAC	8850
rs765951665	in-del	-/AAAGC			intron-variant, downstream-variant-500B	KAT2B, MIR3135A	GRCh38.p7	3:20138129	TGTAGAAAATGTAAT[-/AAAGC]AAAAGAAGGAAAGAA	8850
rs766015408	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20104868	AAGAAAAATATAAGT[A/G]TTCTTTTTTTGTTGT	8850
rs766031840	in-del	-/G			intron-variant	KAT2B	GRCh38.p7	3:20046010	GTGATCTTAGGCACA[-/G]GTCACTTAGTTTTTC	8850
rs766036186	in-del	-/A			intron-variant	KAT2B	GRCh38.p7	3:20113943	TGGTTCAGGGAAAAA[-/A]TGAAGAAGACCACTG	8850
rs766072546	snp	G/T	1.70336e-05	0.00291831	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20147999	GTGGAAAAGAGAAAA[G/T]GTAAGTATGACGGGC	8850
rs766077980	snp	A/C/T	8.2549e-05	0.00642406	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20119708	AAAGCCTCTTCTGGA[A/C/T]TTGAGGCAAACCCAG	8850
rs766104919	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20119999	TGGCTGGGCTTGGTT[A/G]CAAGTTACCCATTGA	8850
rs766116877	snp	C/T	3.94438e-05	0.00444076	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20040690	ACCGGGAGGCGGTGG[C/T]TCGGCCCGAATCGCC	8850
rs766147738	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20051655	ACTACTTGCTGAGGC[C/T]ATTAAATGCCACCCT	8850
rs766156407	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20145048	GTGATCCACCCACCT[C/T]GGCCTCCCAAAGTGC	8850
rs766188109	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20101649	ATCATAATATGTTGA[G/T]GTGTGAGGGATGTAA	8850
rs766219587	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20064487	AGATCTTATTGGGTG[A/G]GAAGTTACGGTTTTG	8850
rs766249180	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20143982	GCCCAAACCTCAGCA[A/T]CACACAGTATACCCA	8850
rs766252498	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20073179	AGTTTTTCCTAGATA[C/T]TAAAATTTCAGTCCA	8850
rs766266744	snp	A/C	1.65891e-05	0.00287998	intron-variant	KAT2B	GRCh38.p7	3:20146298	TCCCTAAACACATTT[A/C]CTTCCTGTGCTTTAC	8850
rs766301823	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20114500	CTTAGAGCAGTGCAG[A/G]CACAAAGCAAGCACT	8850
rs766304790	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20085424	AAGTGATGAGGTAAC[G/T]TATTGTATAGTCAAA	8850
rs766319621	snp	G/T	3.3066e-05	0.00406595	intron-variant	KAT2B	GRCh38.p7	3:20140376	GGAGGTAAGCAGGTG[G/T]TTGACTCCCTTACCT	8850
rs766330079	in-del	-/GG/GTGG			intron-variant	KAT2B	GRCh38.p7	3:20130868	AGTGTGTGTGTGTGT[-/GG/GTGG]GTGCGTGCATGTGTG	8850
rs766357990	snp	C/T	1.65162e-05	0.00287365	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	KAT2B, MIR3135A	GRCh38.p7	3:20137004	GCATGACATCCTGAA[C/T]TTCCTCACATATGCA	8850
rs766394753	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20096312	GCTCCATGTGGGTCA[C/T]ATCCATTCCCTACTA	8850
rs766400627	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20046987	CTGGTCCAAAATATT[A/T]ATAGAATTAACAGAA	8850
rs766486939	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20055587	CAGAAGTGGCTTGTC[A/G]TGTGTGAGGCCTGTC	8850
rs766491434	snp	C/G			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038298	TTAATGTTAAATCTG[C/G]GTTCCCTCCCCCAAT	8850
rs766524411	snp	A/G	1.65337e-05	0.00287517	intron-variant	KAT2B	GRCh38.p7	3:20127576	CCCAAGGTCTTAGAA[A/G]AAGAGCAGAATGTGG	8850
rs766543832	snp	A/G	1.84578e-05	0.00303786	intron-variant	KAT2B	GRCh38.p7	3:20148536	AAAACTCTGGATGGC[A/G]GTGTGGGGGACAAAT	8850
rs766557229	snp	A/G	3.33851e-05	0.00408551	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20099885	AAAGTCTATTTTACA[A/G]AGAGGAAAACCTGTG	8850
rs766576676	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20054880	CATCTGTGAGCACCG[A/G]TTAGGGGCCTGTGGC	8850
rs766606577	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20108816	GGCATTAGATTCTCA[C/T]AGGAGCCTGAACTCT	8850
rs766609577	in-del	-/AG			intron-variant	KAT2B	GRCh38.p7	3:20142570	AGTTGTCATTAGTAG[-/AG]AGAGAGAGAGAGAAA	8850
rs766614101	snp	A/C			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039755	TTTTTCCTCTGGCTC[A/C]CGCTAGGGTGGAGGA	8850
rs766616087	snp	C/G			utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20153318	TTCCCTGCCCACAAA[C/G]GCATAAACTTGAAAA	8850
rs766618266	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20148925	AGATTAAAGTACTTG[A/T]CTGCTGTACTTTCAG	8850
rs766623810	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20132620	ACCAAGGCAGTACTT[A/G]AACTACCATGACTGC	8850
rs766641479	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20123145	CAGCAGTTAACATTA[C/T]GCCACATTTGCTACC	8850
rs766703746	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20050051	CTAAAAATACAAATA[A/T]TAGCAGGGCGTGGTG	8850
rs766728301	snp	A/G	1.70041e-05	0.00291577	intron-variant	KAT2B	GRCh38.p7	3:20114854	AGTAGTTTTTTTTTA[A/G]TCTTATTGCTATTAC	8850
rs766735470	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20079936	ATATTTTCTCTGCTC[A/G]TTTGGTATAAGTTAT	8850
rs766752808	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20129184	GTTATAAAAGCACAC[A/G]TATTATGTGCTTTTA	8850
rs766790571	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20078003	AACATGGCGAAACTC[A/C]ACCTCTACAAAAAAT	8850
rs766799213	in-del	-/T			intron-variant	KAT2B	GRCh38.p7	3:20078878	AGAGACTCCCAGAGC[-/T]TTTTTTTTTTTTTTG	8850
rs766824131	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20116878	ATTGGGTTTCACATC[C/T]GTATCTAATTCCTAA	8850
rs766871792	snp	C/T	3.29549e-05	0.00405911	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20072377	GAAAAACCCTAACCC[C/T]TCACCCACTCCCCCC	8850
rs766894799	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20115870	AGTGGAATCATATAG[C/T]AGATAGCTTTTTGAG	8850
rs766908911	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20049648	GAAATTTATTGTACT[A/C]CAATTGAGAGGTATG	8850
rs766908932	in-del	-/G			intron-variant	KAT2B	GRCh38.p7	3:20118747	AAAAAAAAAAAAAAA[-/G]GAGAGAGAGCGAACT	8850
rs766916682	in-del	-/GTT			intron-variant	KAT2B	GRCh38.p7	3:20062873	CCATTGTAAAATTTC[-/GTT]GTTGTTGTTGTTGTT	8850
rs766931880	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20127269	AAAAGTTCAGATAAA[A/C]GGATGGTCTAGCGAG	8850
rs766957958	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20118147	ATAAAAAAAAATTTA[C/G]GAGAAAAAAATTAAA	8850
rs766971872	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20089947	GAATTTGAGAAGAAC[A/G]GCTTGGACAACATAG	8850
rs766980810	in-del	-/C			intron-variant	KAT2B	GRCh38.p7	3:20053360	GGCAACATAATGAGA[-/C]CCCCATCTCTATAAA	8850
rs766985807	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20098225	ACAGAGTGAGACAAC[A/G]TCCCAAATTAAAAAA	8850
rs766994810	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20060037	ATGTGTTTGAGATAC[A/G]TCCATGTTGTAGCAT	8850
rs767040126	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20111518	TATAGTTAATAGTAC[A/G]AGATAAACATAATTG	8850
rs767042302	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20087135	GAATGAGTTCTAGTG[C/T]TCTATGCCACTGTAA	8850
rs767045793	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20141137	CTTCTCTAGCACCAG[A/T]TTGATCCACCTATTT	8850
rs767046913	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20071889	CGGTTCTATGGGTTT[C/G]CCTTCTGGTCCATGG	8850
rs767052616	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20083001	TCAAAACAGTAGGGG[A/G]TGCTTATTAATTTTC	8850
rs767061655	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20088814	TTCAAAAAATCTTTG[C/T]GAAGACCAATGTCAA	8850
rs767087293	snp	A/C/G	0.000115693	0.00760488	intron-variant	KAT2B	GRCh38.p7	3:20148349	CAAATATTTTGAAAT[A/C/G]ATTTCCCACATGGAA	8850
rs767211822	snp	A/C	0.000174373	0.00933574	intron-variant	KAT2B	GRCh38.p7	3:20095451	TTCTCTCATTATTCA[A/C]ATGTACCCAGTCTCC	8850
rs767218896	snp	G/T			utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20154070	TCATGATACAGTTTG[G/T]ATTAAGTATCTTGGA	8850
rs767252159	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20109806	ACACTTAAGATACCC[A/C]TTTCAGTATTGTAAA	8850
rs767282085	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20133606	TTCTGGTAATTTTCT[A/G]TCATCAGCAATGTTC	8850
rs767323005	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20080754	AATTGTGCTGTAAGC[G/T]TGAAATGCACACAGG	8850
rs767328405	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20092648	TTATATCCTCTTGAT[A/G]AATTGATCCCTTTAT	8850
rs767330656	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20054645	TTGTGTGGTATGCAG[G/T]AGGTTCCAGAAGTAC	8850
rs767356489	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20093247	AATAAAGAGTGAATT[A/C]CTAAGCCAGCTCTCA	8850
rs767371939	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20132801	TATTTACCAAAGAAC[C/T]ATTGTTGTTCTTGAG	8850
rs767372484	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20043493	CTGGTAGGGTGGGAT[C/T]GGCTTCCTGGAGGAA	8850
rs767377212	snp	C/G			missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20072390	CCCTCACCCACTCCC[C/G]CCAGAGCCGACCTGC	8850
rs767384311	snp	C/T	1.97221e-05	0.00314017	intron-variant	KAT2B	GRCh38.p7	3:20040817	ACCGCGGATGGGTGC[C/T]AGGGGCCCAGCCCGC	8850
rs767409837	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20057253	GTATTGGGATGGAGG[A/G]CAAGCCTTTTTGTAA	8850
rs767416068	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20102591	TAGTCTTGGATTGAA[C/G]ATATATTTTCTTCTA	8850
rs767417068	snp	C/T	1.6525e-05	0.00287441	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20122753	TCCGATGGAATTAAT[C/T]AACGAGGTTATGTCT	8850
rs767428322	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20075299	ATATAATAGTATAAA[A/G]CTTTTTTCTATTTTA	8850
rs767446392	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20103865	TCTCTCCCTTTTTAC[A/G]TGAGCTTTAGACCAG	8850
rs767461506	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20145260	TTTAAAAATGCGGCT[A/G]GTAGAAAAATTTAAA	8850
rs767470394	snp	C/T	1.77109e-05	0.00297576	intron-variant	KAT2B	GRCh38.p7	3:20122646	ACCACCCATTGTTTG[C/T]CTTTTATTTTGATCA	8850
rs767470529	snp	C/T	1.65677e-05	0.00287812	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20146419	TTCCTATAGAAAGCA[C/T]TCCTGGAATTAGTAC	8850
rs767549732	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20144226	TCAAATTGAAACAGT[C/G]TTCAGCATATTCTCT	8850
rs767572232	snp	C/G/T	6.60146e-05	0.00574487	intron-variant	KAT2B	GRCh38.p7	3:20119582	CTAACACCTTCTTCT[C/G/T]CTTTTGCCGGGGCAG	8850
rs767623469	snp	G/T	1.73039e-05	0.00294137	intron-variant	KAT2B	GRCh38.p7	3:20140178	GCACTCAGTAGATAT[G/T]TGGTGTATGGTGTTC	8850
rs767635082	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20041510	TCAGTTTGAGGACAC[C/T]CATTTCTTGCTACCC	8850
rs767640176	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20063759	TGTTGGCCAGGCTGG[C/T]CTTGAACTCCTGACC	8850
rs767656919	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20074350	TATCAGCCTGAGTTC[A/G]AATCCTAACTCTATA	8850
rs767676495	snp	G/T	3.38341e-05	0.00411289	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20137056	TTTAAGAAACAGGTT[G/T]GTTTCTCACCACGCA	8850
rs767692961	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20085967	AATTCCTCTCTTCTT[A/G]CCTTTTAAAAATGCT	8850
rs767713614	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20114577	AGCTATATGGAGGGC[C/T]GAAATCGTGCTCTGA	8850
rs767728550	snp	C/T	0.00010185	0.00713546	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152533	ACAAGTGATTTTTTT[C/T]CCCCTCTGCTTCTTA	8850
rs767729527	in-del	-/GAG			intron-variant	KAT2B	GRCh38.p7	3:20115013	CTTTTACATGAATCA[-/GAG]AACAACCAGGGAGGC	8850
rs767801784	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20113598	TAAATCCTTTTCACC[A/G]AATATGACAACATTT	8850
rs767826775	snp	C/T			intron-variant, downstream-variant-500B	KAT2B, MIR3135A	GRCh38.p7	3:20138083	AACATTTTCATTTAC[C/T]TTTCTGACTATAAAA	8850
rs767845859	snp	A/C	6.60338e-05	0.00574566	intron-variant	KAT2B	GRCh38.p7	3:20072482	CCTAAATCTTCAAGG[A/C]AAGTATAACGAGTTC	8850
rs767898192	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20123928	ATTTCTTAAGACATA[C/T]CTGTCTTAAGACATT	8850
rs767911128	snp	A/G	4.94287e-05	0.00497111	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20125960	CAAGGTTGGAAGAGC[A/G]CAGGGGTGTAATTGA	8850
rs767947876	snp	A/C/T	3.36424e-05	0.00410125	intron-variant	KAT2B	GRCh38.p7	3:20095225	ATGTTTGGTTTCCAA[A/C/T]TGAGGTCTTACATAT	8850
rs767959187	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20106357	GGAGGAATACATGTG[C/T]TCATGCACGTCCGTT	8850
rs767967905	snp	C/T	1.64939e-05	0.0028717	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20148260	AAGAGCCCAGAGACC[C/T]TGACCAGCTTTACAG	8850
rs767968078	in-del	-/AT			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070627	CTTATACTGTTACAC[-/AT]ATATACACACTTCAG	8850
rs768015791	snp	A/G	1.65921e-05	0.00288024	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20114964	TCAGCCTCTTCCAGA[A/G]CCAGCCAGCTAGGCA	8850
rs768049210	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20062614	TTACAGGCATGCGCC[A/G]CCACGCCCAGCCAAT	8850
rs768055355	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20081892	TCATATATATATATG[C/T]ATAAATGTATATAGA	8850
rs768195217	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20091434	TTTTTTTTATCTTTT[C/G]AAAGAACCAACTTTT	8850
rs768202883	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20078293	CTATTGTTATTTTGG[A/G]GTCCATTGTTCTGAA	8850
rs768208907	in-del	-/AC	1.64876e-05	0.00287116	frameshift-variant, intron-variant, nc-transcript-variant	KAT2B	GRCh38.p7	3:20127426	TTATTCTTTCAGGAA[-/AC]ACAAAACCCTTGCTT	8850
rs768239853	snp	G/T	1.79519e-05	0.00299593	intron-variant	KAT2B	GRCh38.p7	3:20111831	TTGATCCCAGAGCTT[G/T]AGGTTGCTAAATACA	8850
rs768255475	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20113322	TTGTCATTCTGTCTC[C/T]GAGTCAAGGTACAAA	8850
rs768291648	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20055299	CAAATTGTTATTTAA[A/T]GTGCCAGGTGTTGAT	8850
rs768307155	snp	A/C	7.20292e-05	0.00600079	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20137094	TTTGTCACTCCTTTT[A/C]TTAATATGTTCTCAG	8850
rs768359872	snp	C/T	3.30945e-05	0.0040677	missense, utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152460	AGTGAATACTACAAA[C/T]GTGCCAATATCCTGG	8850
rs768368635	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20056146	AAACAGTAGATAAAG[A/T]GGGCCAGTTGGAAGT	8850
rs768395523	snp	A/C			intron-variant, downstream-variant-500B	KAT2B, MIR3135A	GRCh38.p7	3:20137677	AAGTAGCTGTGACTA[A/C]ACCCAGCTAATTTTT	8850
rs768408934	in-del	-/TTT/TTTT			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070309	TTCTTTCTTTCTTTC[-/TTT/TTTT]TTTTTTTTTTTTTTG	8850
rs768435794	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20046402	GCCTGGGCAACATGG[C/T]GAAACCCTGTCTCTA	8850
rs768482330	in-del	-/AC			intron-variant	KAT2B	GRCh38.p7	3:20142905	TGTGTGTGTGTGTGT[-/AC]GTACATATACCTATG	8850
rs768489478	snp	C/T	1.65463e-05	0.00287626	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20125910	TGCATCTCAGACCAA[C/T]TTTCTGTCAGCACAC	8850
rs768506289	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20061019	ATCTGAACTATTTTT[A/G]AGTGTCTAGTTCATT	8850
rs768513053	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20108007	TAGAGATGGGGTTTC[A/T]TCATGTTCCCCAGGC	8850
rs768530791	snp	A/G	1.64814e-05	0.00287061	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20072410	AGCCGACCTGCAGCA[A/G]ATAATTGTCAGTCTA	8850
rs768585725	snp	A/C			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038923	TCACTGTTTAGATCT[A/C]CAAACTCCCCCACCT	8850
rs768622514	snp	A/G	5.75921e-05	0.00536588	intron-variant	KAT2B	GRCh38.p7	3:20040794	AGGTACGCGCTCGCC[A/G]CTCTCGGACCGCGGA	8850
rs768632240	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20067130	GGAAGTCTCAGTCAT[A/T]ATGAACAAAAGAAAT	8850
rs768663728	snp	A/G	1.6638e-05	0.00288422	intron-variant	KAT2B	GRCh38.p7	3:20146276	GAACTGTATCCATAG[A/G]CTTCTTTCCCTAAAC	8850
rs768665623	in-del	-/CA			intron-variant	KAT2B	GRCh38.p7	3:20050419	ACATTTTCAGCATCT[-/CA]GAGGGTTCTCTTGTG	8850
rs768668750	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20077712	TATTGAATTGTGCTG[C/G]TTTAGAATATTCTAG	8850
rs768677305	in-del	-/CAA			intron-variant	KAT2B	GRCh38.p7	3:20152242	AAAATGTAATCAAAC[-/CAA]CAACATAGATTCCTT	8850
rs768678029	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20097689	TTACAGGTGTGTGCC[A/G]CCATGCCCGGCTAAT	8850
rs768706191	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20117431	TTCATAAGGATGAAC[C/T]TGAAATTTTACAAGA	8850
rs768722036	snp	G/T	1.8011e-05	0.00300087	intron-variant	KAT2B	GRCh38.p7	3:20122627	TATTTGTTTTGTGTT[G/T]AGAACCACCCATTGT	8850
rs768732961	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20117263	ACCAAGTTAAGTTGG[C/T]GTGTACACTTTAGTA	8850
rs768756768	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20089602	AGATGGGTTTTCACC[A/G]TATTAGCCAGGCTGG	8850
rs768816916	snp	A/T	1.64898e-05	0.00287135	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20111674	GGTGTTTGGGAGAAC[A/T]TTGCTTCGCTCGGTC	8850
rs768821743	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20049833	TCTGTTGAAGAAAGA[C/T]GAAAGAGACACCTAC	8850
rs768928628	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20068089	GCAACCTCTGCCTCC[C/T]GGGTTCAAGCGATTC	8850
rs768979614	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20044878	GAATGAACCAGAGAA[G/T]AGAAAATGGAAGAAA	8850
rs768988027	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20098860	GGAGTTGAGGTCCTT[G/T]TAAGACACAGTTCAG	8850
rs768996722	in-del	-/ATTA	1.67105e-05	0.0028905	frameshift-variant, utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152510	AATTAAGGAAGCTGG[-/ATTA]ATTGACAAGTGATTT	8850
rs769003551	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20059856	AGAAGATTTCCATCA[A/C]CTCCAAAGGATCCTT	8850
rs769025990	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20141665	GTTAGGCATTATCTA[C/T]CTAACAGCCCTAAAG	8850
rs769036453	snp	A/G	1.74042e-05	0.00294988	intron-variant	KAT2B	GRCh38.p7	3:20099846	CTTTTTCTTTTTTTT[A/G]ATGATTTCTTTGCAG	8850
rs769054500	snp	C/T	0.000110162	0.00742086	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20040677	GCACGGCCGAAGGAC[C/T]GGGAGGCGGTGGCTC	8850
rs769055854	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20053280	TGTAATCCCAGGTGT[A/G]GGATCCTACTTTTGG	8850
rs769073240	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20043812	CTCTCTCAGCTTGTT[G/T]CTGCACTTAATATGA	8850
rs769093948	snp	A/G	4.97277e-05	0.00498612	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152375	GAATAGGTACTACGT[A/G]TCTAAGAAATTATTC	8850
rs769106490	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20082481	TTTTCCTTTCCATTA[A/G]GCCTCCACTCAAGAA	8850
rs769126094	snp	C/T	3.34035e-05	0.00408664	missense, utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152352	AAAACCATGAGTGAA[C/T]GCCTCAAGAATAGGT	8850
rs769138850	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20094029	CAGTTTCAAACCCTA[A/G]CTCTGCCTTGTTGGC	8850
rs769145877	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20065442	GGAGACCTCTTATCT[C/T]GAAGAACAGTGGCCA	8850
rs769165203	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20148518	TTTTCTAAGTATAGA[C/T]TTAAAACTCTGGATG	8850
rs769171342	in-del	-/C			intron-variant	KAT2B	GRCh38.p7	3:20128479	CATGTGTTGGAGTGT[-/C]CTTTTTGTTTTGTTT	8850
rs769183925	in-del	-/C			intron-variant	KAT2B	GRCh38.p7	3:20104370	CAACCTCCCCCACGT[-/C]CCCCACCATCACGTC	8850
rs769210466	in-del	-/A			intron-variant	KAT2B	GRCh38.p7	3:20126822	GCGAAACTCCATTTC[-/A]AAAAAAAAAAAAAAA	8850
rs769236702	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20121617	AAAAGATAAAGTGTG[C/T]CATTTTATAATAGAA	8850
rs769282141	snp	C/T	1.67089e-05	0.00289035	intron-variant	KAT2B	GRCh38.p7	3:20148206	CAATAGGGTAAAACT[C/T]TAATCATTGCTCCTT	8850
rs769328397	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20133052	TTTTAGAAATAATTT[C/T]TAATTATGTAAGACA	8850
rs769385091	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20145877	GACTTTCTGGGGCCC[A/G]TTTACCTGCTTCTCT	8850
rs769406695	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20102263	AGAGTTTGCAGTGAA[C/T]TGAGATCGTGCACTC	8850
rs769425465	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20145003	GGTTTCACCGTGTTG[G/T]CCAGGCTGGTCTCGA	8850
rs769429837	snp	C/G	0.000131924	0.00812063	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20140285	TCAAGGATTATGAAG[C/G]AGCCACTTTAATGGG	8850
rs769438323	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20047516	GTAACTATGCTGCTT[C/T]TGAGTTAATGTATGC	8850
rs769459234	snp	A/T	1.64846e-05	0.0028709	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20072426	ATAATTGTCAGTCTA[A/T]CAGAATCCTGTCGGA	8850
rs769486889	snp	A/G	3.3475e-05	0.00409101	intron-variant	KAT2B	GRCh38.p7	3:20148193	AGTAATCAGCTGGCA[A/G]TAGGGTAAAACTCTA	8850
rs769489207	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20124754	TCAGGAGTTTTGTGA[A/G]CTGGTTGTTCCATAT	8850
rs769492861	in-del	-/AT			intron-variant	KAT2B	GRCh38.p7	3:20062099	TATTATATATAAAAC[-/AT]ATAATATATATTATA	8850
rs769494428	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20114442	ACAAATAAAAATAGA[A/G]TATATAACTCATAGG	8850
rs769510529	snp	C/T	3.53769e-05	0.00420562	intron-variant	KAT2B	GRCh38.p7	3:20115034	AACCAGGGAGGCCAA[C/T]CTGAAGTGTAAGTTG	8850
rs769511836	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20097427	TCAGCATTCTCCCCA[C/T]CTCCTGCAAAAAGTA	8850
rs769547391	snp	A/G	3.3077e-05	0.00406662	intron-variant	KAT2B	GRCh38.p7	3:20127402	GATAGGTAAAACTTT[A/G]ACATAATCTTATTCT	8850
rs769554331	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20125820	GTATCTTATTAGAAC[A/G]AAGATGAGAAGCTTG	8850
rs769566860	in-del	-/AAAC			intron-variant	KAT2B	GRCh38.p7	3:20044095	AAGAAAAAAGAAAAG[-/AAAC]AAACAAACTTGTTTC	8850
rs769597236	snp	G/T	1.73405e-05	0.00294448	intron-variant	KAT2B	GRCh38.p7	3:20111555	TCTGATGACCTGGGG[G/T]TTTATGGGATATTGA	8850
rs769601797	snp	A/G	2.21364e-05	0.00332682	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20126078	CCAGCTGCCCCGAAT[A/G]CCAAAAGAATACATC	8850
rs769655840	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20086449	ACGGAAAATACAAAA[A/C]AATTAGCCAGGCATG	8850
rs769656875	snp	C/T	1.64955e-05	0.00287184	intron-variant	KAT2B	GRCh38.p7	3:20148315	GGTGAAGGTGGGTGT[C/T]CTCTTTATTCACCTC	8850
rs769657817	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20073943	AGCCGAGCAGATTGT[C/T]TCCATTCTAAGCACG	8850
rs769719682	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20068857	TTAGTCATTTTTCTT[A/T]CTCTAACTTAAGGTC	8850
rs769729991	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20061155	CTCTTCCTTCCTCCA[A/G]CCCCTCGGCAACCAC	8850
rs769749403	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20096232	TGTTACCTGTTTCTC[A/G]CTGACACCAGTCACC	8850
rs769763836	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20109915	TTAATTTTTAATGTA[C/G]GCAGATGAACTAACA	8850
rs769772021	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20081414	TTGGCAGCAGTCACA[C/T]GGCGGGTCACTCTCT	8850
rs769776772	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20105980	AGATTTATCAGGAAG[C/T]ATGGAAAGAACACTA	8850
rs769795235	in-del	-/AAAAAAAAAAAAA			intron-variant	KAT2B	GRCh38.p7	3:20058454	GCGAGACTCTGTCTC[-/AAAAAAAAAAAAA]AAAAAAAAAGGTTTT	8850
rs769812469	snp	A/G			intron-variant, downstream-variant-500B	KAT2B, MIR3135A	GRCh38.p7	3:20137902	ATCCTAGTACTTTGG[A/G]AGGCCAGGGCAGGAG	8850
rs769815129	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20134002	TTTTTGATATTAAAT[C/G]TTTGTAATATATGTT	8850
rs769815761	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20068326	TCAACACGTCTTTAC[A/C]CACTGCGCTGTAGCC	8850
rs769820920	snp	A/G			intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20136522	CTAGTGAAGATTAGC[A/G]CTTTTCATTTGCATC	8850
rs769829584	in-del	-/TAA			intron-variant	KAT2B	GRCh38.p7	3:20133487	TGCAGGAATTTCTAT[-/TAA]TGCTGATATATAGCT	8850
rs769848771	in-del	-/T	0.000935195	0.0216038	intron-variant	KAT2B	GRCh38.p7	3:20114844	TTATCCTTACAGTAG[-/T]TTTTTTTTAATCTTA	8850
rs769876529	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20099674	ACCTGATAGTTGCCC[A/G]TTTTATTGACTTAAG	8850
rs769898227	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20151114	CTTTGTGTTTCTTAG[C/T]GCTTTTAGATTTTTA	8850
rs769954271	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20117564	GAGCCTGGCACTTTA[A/G]TATATTCTGATTTTT	8850
rs769965806	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20042080	AATGTGCATGGGAAT[C/T]TCCTGGGGAAGCTGG	8850
rs769969403	snp	A/G	6.59272e-05	0.00574101	intron-variant	KAT2B	GRCh38.p7	3:20072320	TTTGTCTCTTTCTTT[A/G]TTCCATTTTTAGGCC	8850
rs769995400	in-del	-/AG			utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152621	GACATGATGTATTGA[-/AG]AGACTTGTAAATGTA	8850
rs769997231	in-del	-/TTT			intron-variant	KAT2B	GRCh38.p7	3:20050706	TCATGGGATGAATCT[-/TTT]TTTTTTTTTTTTTTT	8850
rs770018553	snp	C/T	9.02535e-05	0.00671704	intron-variant	KAT2B	GRCh38.p7	3:20147914	TAACTATGTTATTCT[C/T]TTGACCAAAAGCACT	8850
rs770032609	in-del	-/GAAAG			intron-variant	KAT2B	GRCh38.p7	3:20110692	AAAAAAAAAAAAAAA[-/GAAAG]AAAAAGAAAGAAAAA	8850
rs770052552	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20101169	AAGGAAGAGATTTTT[A/G]TGAATAGAGAAATGT	8850
rs770056827	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20051017	ACCAGCCTGGCCAAC[A/G]TGACAAAACCTTGTT	8850
rs770060825	snp	C/T			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039688	TTTATTTTGGTGAAT[C/T]AGCAACAAAGAAAAA	8850
rs770075217	snp	A/G	0.000148924	0.00862785	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20146409	GTTCGACAGATTCCT[A/G]TAGAAAGCATTCCTG	8850
rs770104400	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20060006	CTTTTATGATGGGCT[G/T]CTTATGCCGAGTGTA	8850
rs770108858	snp	A/G	1.6588e-05	0.00287988	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152477	TGCCAATATCCTGGA[A/G]AAATTCTTCTTCAGT	8850
rs770148293	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20060744	AGCGTGAGTAACATA[A/G]TAAGACCCTGTCTCT	8850
rs770148575	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20049928	AGTCCAGCTGGGCAC[C/T]GTGGCTCCCCCTTGT	8850
rs770154341	in-del	-/C			intron-variant	KAT2B	GRCh38.p7	3:20074775	ATTTAGGATTCAACT[-/C]CCAACTGCCTCTGTC	8850
rs770213985	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20117706	GTGGCTGTGTTGAAA[C/T]GTAGATGAACGTTCT	8850
rs770214374	snp	G/T			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20069693	ACCATACCCGGCTAA[G/T]TTTTGTATTTTTAGT	8850
rs770229343	snp	A/G			utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20153760	CATCTTGATGGTCTC[A/G]ACACTAATTTTTATG	8850
rs770233547	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20107607	AGTTGCAGTGAGTCG[A/C]GATCATGCCATTGCC	8850
rs770261467	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20088654	ATATTAGCTTCATCA[A/G]ATGTATGGTGTGAAA	8850
rs770271757	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20083911	CGTGATGGTGGTGCA[C/T]CTATTTTGTTGGGAT	8850
rs770299133	snp	A/G	1.66217e-05	0.0028828	missense, utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152362	GTGAACGCCTCAAGA[A/G]TAGGTACTACGTGTC	8850
rs770312847	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20087016	TGAACTCCTGACCTC[A/G]TGATCCACCTGCCTT	8850
rs770371640	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20082899	CCAAGCAAAGGAACT[A/C]AAATTGGCAGGTACA	8850
rs770391112	snp	C/T	1.71602e-05	0.00292913	intron-variant	KAT2B	GRCh38.p7	3:20101267	AGCTGCATGAAGAAA[C/T]TGCCTTCCCTCTTTT	8850
rs770396097	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20112258	ACTTGCCCCCACTCT[C/T]TGGAAACTAGACTGC	8850
rs770411932	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20106487	CTCTCTCACACACAC[A/G]CACATTGACTCAGCC	8850
rs770425092	snp	C/T	2.78006e-05	0.0037282	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20126097	AAAGAATACATCACA[C/T]GGCTCGTCTTTGACC	8850
rs770461699	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20094329	ATGAGAACTCACTAT[C/T]ATGAGAACAGCATGG	8850
rs770487291	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20121841	CATGAACAAGCCTGC[C/G]AAGATTGAATGAGAT	8850
rs770558843	snp	A/G	3.3195e-05	0.00407387	intron-variant	KAT2B	GRCh38.p7	3:20119751	GAGGGGATAAGAGAG[A/G]GCTGTGACTTGCTCC	8850
rs770577339	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20133520	ACTTTATTCTTTTTA[C/T]ACAGTATTTTATAAT	8850
rs770592770	snp	C/G			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038625	CTGCAAGGTGGAACC[C/G]AAGCTCTTATTAGTA	8850
rs770598367	snp	C/T	1.65715e-05	0.00287845	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20095345	GGATGTGGAATATCT[C/T]TTTACCTGTGTCCAC	8850
rs770602277	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20058404	ACATTGCAGTGAGCC[A/G]AGATTGCGCCACTGC	8850
rs770609904	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20128721	CCTTAGAATGTTATT[C/G]ATTTAGGGCTGGGCA	8850
rs770616447	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20066939	TCATAACACATCTCA[A/G]TTTTTATTGCCAATT	8850
rs770651239	snp	A/C	1.6601e-05	0.00288101	intron-variant	KAT2B	GRCh38.p7	3:20072511	TCATTGTAGCGTGAG[A/C]CTCTTAACTTACTGA	8850
rs770682628	snp	C/T	3.36802e-05	0.00410353	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20111779	TCTAATCCTCACTCA[C/T]TTCCCAAAGTAAGGG	8850
rs770687714	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20116273	GTGCTATTCACTTTA[A/C]CTTGGATTTGATCTC	8850
rs770704633	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20065773	AATAGGGTATAACTT[A/T]AAAGAGTTAGGACCA	8850
rs770730357	in-del	-/A			intron-variant	KAT2B	GRCh38.p7	3:20059412	CAGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	8850
rs770736546	snp	G/T	0.000117431	0.00766169	intron-variant	KAT2B	GRCh38.p7	3:20040811	TCTCGGACCGCGGAT[G/T]GGTGCTAGGGGCCCA	8850
rs770743880	snp	G/T	1.64895e-05	0.00287132	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20111682	GGAGAACATTGCTTC[G/T]CTCGGTCTTCACTGT	8850
rs770748607	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20098348	TGGAGTCTAACTACC[A/T]GGGTTTAAAACTTTG	8850
rs770764489	in-del	-/TCCATC			intron-variant	KAT2B	GRCh38.p7	3:20059849	ACCTTTTAGAAGATT[-/TCCATC]ACCTCCAAAGGATCC	8850
rs770772318	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20048600	GGAGCAGTCAGCACA[A/T]CTGCTTCTCAGATGA	8850
rs770798889	snp	C/T	1.64814e-05	0.00287061	missense, intron-variant, nc-transcript-variant	KAT2B	GRCh38.p7	3:20127434	TCAGGAAACACAAAA[C/T]CCTTGCTTTAATTAA	8850
rs770854511	in-del	-/A			intron-variant	KAT2B	GRCh38.p7	3:20064786	TGTTGGATCAGTTAT[-/A]ACTGAATAAATTTTC	8850
rs770859350	in-del	-/T			intron-variant	KAT2B	GRCh38.p7	3:20044427	CCCTAAAAAAAAAAA[-/T]AAATAAATAAATAAA	8850
rs770864312	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20047796	TTTTTTTGTATTTTT[A/G]GTAGAGACGGGGTTT	8850
rs770877886	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20086555	GCAGTGAGCCAAGAT[C/T]GCACCATTGCACTCC	8850
rs770880255	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20075031	AGCACTTTGGGAGGC[A/C]GAGGCTGGCAGATCA	8850
rs770941469	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20126305	ACAATTTACAAATTT[C/T]CTTGTTAATGATGAT	8850
rs770983812	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20042867	TCCTGGTCACTTTCA[G/T]GACCCAACAAGAGAA	8850
rs770986993	snp	A/C	1.68007e-05	0.00289828	missense, utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152521	CTGGATTAATTGACA[A/C]GTGATTTTTTTTCCC	8850
rs771014472	in-del	-/A	1.65793e-05	0.00287913	intron-variant	KAT2B	GRCh38.p7	3:20119742	AGCTCTTAAGAGGGG[-/A]TAAGAGAGGGCTGTG	8850
rs771031417	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20125051	ACATGAGGCCGGGCG[C/T]GGTGGCTCAGCCTGT	8850
rs771105112	snp	A/G	1.6486e-05	0.00287102	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20101406	GCATCTGGAGGCACC[A/G]TCTCAACGAAGACTG	8850
rs771156251	snp	C/G	1.66153e-05	0.00288225	intron-variant	KAT2B	GRCh38.p7	3:20125893	AATTTTTTCCTGTCT[C/G]TTGCATCTCAGACCA	8850
rs771192776	in-del	-/A	3.3521e-05	0.00409382	intron-variant	KAT2B	GRCh38.p7	3:20148200	AGCTGGCAATAGGGT[-/A]AAACTCTAATCATTG	8850
rs771195931	snp	A/G	1.64939e-05	0.0028717	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20119669	CTTGAGCAGCCAAAC[A/G]CAGGGAGCAGCAGTC	8850
rs771200519	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20042174	ACTCCCAAGTGATGC[C/T]ATGCTAGTCCACAGA	8850
rs771208264	snp	A/C/G	0.00088271	0.0209934	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20040642	CGCCTGCGGTCCGGC[A/C/G]ACGGCAGTGGCTGCA	8850
rs771209664	snp	C/T	1.67346e-05	0.00289258	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20122793	GACCCTGCAGCAATG[C/T]TTGGACCAGAGGTCA	8850
rs771262627	in-del	-/CTAGCA			intron-variant	KAT2B	GRCh38.p7	3:20080012	TTCAAGTTCCTGCCT[-/CTAGCA]CTGGCTGAATTTAGG	8850
rs771321091	snp	A/G	6.63405e-05	0.00575898	intron-variant	KAT2B	GRCh38.p7	3:20140405	CTTCTGTACAGGCCA[A/G]TCTTAGCTGGGGTGG	8850
rs771322400	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20051796	AATGGCTGATTCATT[G/T]GAACCATCCACTTAT	8850
rs771337770	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20130518	TTGTAATTTTAGAAA[A/C]AGATGGCGTAATTTT	8850
rs771355514	in-del	-/TATGTGTGTGTGTGTG			intron-variant	KAT2B	GRCh38.p7	3:20121731	ACATACACATATGCA[-/TATGTGTGTGTGTGTG]TGTGTGTGTGTGTGT	8850
rs771381627	snp	C/G			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20071042	AAAGTTTGGATAACT[C/G]TATTACAAAAGTAAA	8850
rs771420454	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20073537	GTCATCACATTGGAA[A/T]AACCTTCTGAAAATA	8850
rs771421070	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20084968	TAGCACCTTAATTAG[A/G]TGGTTTCATATTATG	8850
rs771426760	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20061001	GATGATCTAAAGTTT[A/G]CCATCTGAACTATTT	8850
rs771514707	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20072652	TGCTGCACTGTGTGC[A/G]GTGACTTTGTCCCTT	8850
rs771530564	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20101103	TCACTTTTCATCCAC[C/T]GTGATCTGAGGCAAG	8850
rs771554287	in-del	-/CTTTTTTTTTTTTTT			intron-variant	KAT2B	GRCh38.p7	3:20063534	CTTCTGAGTAGGCCT[-/CTTTTTTTTTTTTTT]TTTTTTTTTTTTTTT	8850
rs771607683	snp	C/T	1.64893e-05	0.0028713	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20111689	ATTGCTTCGCTCGGT[C/T]TTCACTGTTATGAGG	8850
rs771629729	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20112311	AGAGAGCTCCTTCAG[C/T]GTGATGAACCTCTAT	8850
rs771633611	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20058935	TCTCAGGTTCCACCC[G/T]ACACCCACTGAATCT	8850
rs771660443	snp	C/T	6.59022e-05	0.00573993	missense, intron-variant, nc-transcript-variant	KAT2B	GRCh38.p7	3:20127457	TTAATTAAAGATGGC[C/T]GTGTTATTGGTGGTA	8850
rs771673032	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20089357	AATTCTTCCAATCTG[C/T]GAACATAAAAGATAT	8850
rs771675789	snp	A/G			intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20136036	GACCTCTAGCCTCAT[A/G]TGGATTAGGGGGTTA	8850
rs771703439	snp	A/C/G	9.93542e-05	0.0070475	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20122724	GCCAAGAAACCCCGA[A/C/G]TTATGGGGGATATTC	8850
rs771749672	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20134568	CACGTGCCACCACGC[C/T]CAGCTAATTTTTGTA	8850
rs771757229	snp	C/G	3.51549e-05	0.0041924	intron-variant	KAT2B	GRCh38.p7	3:20152323	CTAATATTTTTTTTT[C/G]CTGTGCAGATCTGAA	8850
rs771799250	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20077644	GAATATGTTGGGTTA[A/T]TGTATTATTAAAATT	8850
rs771831244	snp	A/G			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039372	TTTCCTGGTTAATAC[A/G]CACGCGGTGGCACAA	8850
rs771849982	snp	C/T	1.74181e-05	0.00295106	intron-variant	KAT2B	GRCh38.p7	3:20111810	AGAGTTTTTGCTGGT[C/T]TTTGTTTGATCCCAG	8850
rs771888629	snp	A/G	1.64773e-05	0.00287026	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20072336	TTCCATTTTTAGGCC[A/G]AGGAGTCTTGTAAAT	8850
rs771919200	snp	C/G			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038676	GGTTGATCAGAGAAG[C/G]ACAGCCTTTAAGACT	8850
rs771924792	in-del	-/A			intron-variant	KAT2B	GRCh38.p7	3:20128915	GGAGGCTGAGGCAGG[-/A]AAAATTGCTTGAACC	8850
rs771929406	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20146579	AGAAGGCAGCAAATG[C/T]TACCCTTTTATGTCT	8850
rs771977841	snp	A/G	1.76789e-05	0.00297307	intron-variant	KAT2B	GRCh38.p7	3:20147939	AGCACTTCTCATTCA[A/G]TGTTTCACTTTGTTG	8850
rs772002333	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20105015	CTTAGCCTCCCAAGT[A/G]GCTAGGATTACAAGT	8850
rs772034404	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20126355	TGCTGATGACTCTCC[C/T]GTGCTTCATTCTTTA	8850
rs772059137	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20049372	AAGTGTTATGTCTCA[C/T]GACATTTGATTCTTC	8850
rs772068487	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20087813	AGGCTCTCACTTTGT[A/T]GTCCAGGCCAGAATG	8850
rs772091773	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20127950	GGTAATGCTCACTTG[C/T]CTGCCACTCACCTCG	8850
rs772092263	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20116333	AAACTCTTCCCTAAG[C/T]TCTCCCATCCCCTCT	8850
rs772124073	snp	G/T	0.000769777	0.0196035	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20126038	TCCTGATGTGGCTGG[G/T]TGGCCTACAGAACGT	8850
rs772125502	snp	C/T	3.29696e-05	0.00406001	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20140324	TAAATCCACGGATCC[C/T]GTACACAGAATTTTC	8850
rs772131342	in-del	-/A			intron-variant	KAT2B	GRCh38.p7	3:20105802	ACGACCCTGTCTGAA[-/A]AAAAAAAAAAAAAAA	8850
rs772149023	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20059699	GACTGAGCGAGACTC[C/T]ATCTCAAAACAAAAA	8850
rs772160646	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20098536	AGAACTTTTTTTTAT[A/T]TGCACACTTATCCCA	8850
rs772201923	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20043765	GGACTTGATTGGGTA[C/T]GAGGGAGTGTAAGAG	8850
rs772251043	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20121458	AAAAAAACTACCATG[A/C]AATCTCATGAGGAAA	8850
rs772259882	snp	A/G	0.000207104	0.0101739	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20040652	CCGGCGACGGCAGTG[A/G]CTGCAGCGGGCACGG	8850
rs772263983	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20047303	TCTTGAACTCCTGGG[C/T]TCAAGCAATTGGCCT	8850
rs772277545	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20114803	GACGCTGATGTTAAG[A/G]TGATTGTCACAGATA	8850
rs772295868	snp	A/G	1.70026e-05	0.00291565	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20095387	TGCAGATACCAAACA[A/G]GTTTATTTCTATCTA	8850
rs772313252	snp	C/T	1.73745e-05	0.00294737	intron-variant	KAT2B	GRCh38.p7	3:20111548	GAATATTTCTGATGA[C/T]CTGGGGGTTTATGGG	8850
rs772323442	snp	A/G			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20071240	ACTAGCTGGATTTCT[A/G]GTGCTCAATAGCCAC	8850
rs772328121	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20152022	AGCTAACAGTAGTCA[C/G]TTCATCATACTTATT	8850
rs772329625	in-del	-/AAG			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038997	CAGAGAATCTGGAAA[-/AAG]AAGAAGGGGAATGTT	8850
rs772366442	snp	A/G	4.94629e-05	0.00497283	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20101414	AGGCACCATCTCAAC[A/G]AAGACTGCGATCTCC	8850
rs772390952	snp	A/T	1.66866e-05	0.00288842	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20122695	AAATGACTGATTCTC[A/T]TGTTCTGGAGGAGGC	8850
rs772392527	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20109491	CTGGCTGATTTTTAA[A/G]CTTTTTGTAGAGATG	8850
rs772417989	in-del	-/C			intron-variant	KAT2B	GRCh38.p7	3:20054083	GATTACAGGCATGAG[-/C]CATTGTGTCCGGCTT	8850
rs772496832	snp	A/T	1.65993e-05	0.00288086	intron-variant	KAT2B	GRCh38.p7	3:20140410	GTACAGGCCAGTCTT[A/T]GCTGGGGTGGGTTGC	8850
rs772502355	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20120540	GCTGACTTCTGCCTC[A/G]TTCTGTCGTCCAAAG	8850
rs772516362	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20092787	GCTCACTGCAATCTC[C/T]GCCTCCTGGGTTCAA	8850
rs772521582	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20102186	CTGGGCATGGTGTCA[C/T]GTGACTGTAATCCTG	8850
rs772544886	in-del	-/T	0.0101066	0.0703643	intron-variant	KAT2B	GRCh38.p7	3:20152314	CAAAGATTGCTAATA[-/T]TTTTTTTTCCTGTGC	8850
rs772570133	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20064115	AAGGTGGTTGTACCT[G/T]GTTACATCCCACAAA	8850
rs772592541	snp	A/G	1.70679e-05	0.00292124	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20147982	GACAGGCTGGAAACC[A/G]AGTGGAAAAGAGAAA	8850
rs772654072	snp	C/G	1.66532e-05	0.00288554	intron-variant	KAT2B	GRCh38.p7	3:20148215	AAAACTCTAATCATT[C/G]CTCCTTGTTTCCCTT	8850
rs772666423	in-del	-/AG			intron-variant	KAT2B	GRCh38.p7	3:20069091	GTCAGTCAGACTAAC[-/AG]AGAATACATTAACAA	8850
rs772666760	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20132321	GAGGTTGCGGTGAGC[C/T]AAGATTGTGCTATTG	8850
rs772671390	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20132229	AAAATACAAAATTAG[C/T]TGGGTGTGGTGGTGC	8850
rs772755583	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20133112	AATCCCATTTCCCCT[A/T]CCCACTACCATCCTG	8850
rs772756681	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20145013	TGTTGGCCAGGCTGG[A/T]CTCGAGCTCCTCACC	8850
rs772757307	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20130545	TTTTTATTTTCAAAG[A/G]TAGCTATACCAAACA	8850
rs772771300	snp	A/G	1.9071e-05	0.00308791	intron-variant	KAT2B	GRCh38.p7	3:20040785	CCGCCTGCAAGGTAC[A/G]CGCTCGCCGCTCTCG	8850
rs772783892	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20056545	CTCATAGATGTCAGT[C/T]ACTGTTACAATTAAA	8850
rs772826687	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20120750	TTTCACAGTTAGAGA[A/G]TGTTTTGAAGGTTGC	8850
rs772885480	in-del	-/G			intron-variant	KAT2B	GRCh38.p7	3:20091757	TCTGACCCATTGGTT[-/G]TTCAGGAGAATGCTG	8850
rs772944315	snp	G/T	0.000242693	0.0110131	intron-variant	KAT2B	GRCh38.p7	3:20111556	CTGATGACCTGGGGG[G/T]TTATGGGATATTGAT	8850
rs772950002	snp	C/T	1.6492e-05	0.00287154	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20072446	ATCCTGTCGGAGTTG[C/T]AGCCATGCCCTAGGT	8850
rs772973485	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20063343	GCCACCACACCTGGC[C/T]GCCTGTGCTTTTGGT	8850
rs772995262	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20046785	TTTTTCATTTGTCAG[C/T]ATTTAGAGCAGTGGC	8850
rs773002789	snp	C/T	1.64727e-05	0.00286986	intron-variant	KAT2B	GRCh38.p7	3:20119547	TTCGTTTCTTGTTAC[C/T]TAAGAAAGGAGTCAG	8850
rs773027860	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20123716	TGTTTAGTCTCCTTT[A/G]AAACAACTCCCCAGC	8850
rs773037735	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20073130	ATATTTAAAAAAATC[A/G]TGTGTTGTTTGAGTA	8850
rs773072043	in-del	-/T			intron-variant	KAT2B	GRCh38.p7	3:20050706	CTCATGGGATGAATC[-/T]TTTTTTTTTTTTTTT	8850
rs773075158	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20063499	CTGGAGTGCAGTGGT[A/G]CGATCTCACCTCACA	8850
rs773083086	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20068964	CGGCAACTAAGAGAG[G/T]TTGGCCCACAATAAG	8850
rs773085565	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20047695	TCAGTTTACTGCAGC[A/C]TCCACCTCCCGGGTT	8850
rs773091117	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20071874	GATTGCTAACTTCTT[C/T]GGTTCTATGGGTTTC	8850
rs773114824	snp	A/C	2.28752e-05	0.00338187	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20126081	GCTGCCCCGAATGCC[A/C]AAAGAATACATCACA	8850
rs773123954	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20081469	GACACAGCACTGAGA[A/G]GTGCCAAGGTATACC	8850
rs773147919	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20074022	GCCAACTTTGTTTCC[G/T]TTTTTATTTCTTACC	8850
rs773167944	snp	C/G	3.30093e-05	0.00406246	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20125925	TTTTCTGTCAGCACA[C/G]TCGGCCAGGGATGAG	8850
rs773186424	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20040995	AGGGGGATCACTAAG[A/G]CGGAGAGCCCTTCAT	8850
rs773232310	snp	C/T	1.67058e-05	0.00289009	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20122791	CGGACCCTGCAGCAA[C/T]GCTTGGACCAGAGGT	8850
rs773235992	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20085273	ACATAAAAATGTTGA[C/T]CTAATTGTCTGCAGA	8850
rs773292852	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20068361	TGGCCTTTACTTTCT[A/G]TTGAGCAAGCCAGGC	8850
rs773305503	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20061221	CCTTATCTAAGTGGA[A/G]TCATACAGTATTTGT	8850
rs773353383	in-del	-/CTT	1.65117e-05	0.00287325	intron-variant	KAT2B	GRCh38.p7	3:20119574	TCAGTCATCTAACAC[-/CTT]CTTCTCCTTTTGCCG	8850
rs773373698	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20151134	TTAGATTTTTATCTC[C/T]CTCCAAACTGTTTTA	8850
rs773377889	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20049938	GGCACCGTGGCTCCC[C/G]CTTGTAATCCCAGCA	8850
rs773379452	snp	C/T			intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20136565	TCTGAGATTCTCAAA[C/T]ACCTTAAAGATAAGC	8850
rs773429521	in-del	-/AGA			intron-variant	KAT2B	GRCh38.p7	3:20143180	GCTGTGGACTTCAGG[-/AGA]AGAAGATGAGGACAT	8850
rs773436380	snp	C/T	1.64806e-05	0.00287054	intron-variant	KAT2B	GRCh38.p7	3:20072324	TCTCTTTCTTTATTC[C/T]ATTTTTAGGCCGAGG	8850
rs773457566	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20042158	TTTGCATTTCTGACA[A/G]ACTCCCAAGTGATGC	8850
rs773469356	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20150042	CTTGCAGCCTGCTTT[C/T]TGAAAGTGTTTTGCT	8850
rs773498073	in-del	-/GCCTT			intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20137179	GCATTTGTTTTACAA[-/GCCTT]ATGTCAAAAATAAGC	8850
rs773542818	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20129091	GCTCCGGATGATTAA[C/G]ATGGCTGCTGAGAAA	8850
rs773549177	snp	A/G			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039734	GTACTTTTCAAAAAT[A/G]TATTTTTTTTCCTCT	8850
rs773600279	snp	C/G	1.65553e-05	0.00287705	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20146412	CGACAGATTCCTATA[C/G]AAAGCATTCCTGGAA	8850
rs773605058	snp	C/T	3.41892e-05	0.00413442	intron-variant	KAT2B	GRCh38.p7	3:20101270	TGCATGAAGAAATTG[C/T]CTTCCCTCTTTTTAA	8850
rs773619049	snp	G/T	1.66145e-05	0.00288218	missense, utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152363	TGAACGCCTCAAGAA[G/T]AGGTACTACGTGTCT	8850
rs773685312	snp	A/G	0.00128123	0.0252779	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20137529	TTCCTTCCTTTCTCC[A/G]TTCCTCCCTTCCTTT	8850
rs773686140	in-del	-/G			intron-variant	KAT2B	GRCh38.p7	3:20120361	GTCTCCTGAGTAGCT[-/G]GGATTACAGGTGCCC	8850
rs773690090	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20097797	CCCCTCGGCCTTCCA[A/G]AGTGCTGGGATTACA	8850
rs773710809	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20100835	AGAGTTTAAATTTTA[A/G]TTGTTTAGTTCAGTG	8850
rs773719527	in-del	-/AT			intron-variant	KAT2B	GRCh38.p7	3:20151478	CTTATTTTTCCACAC[-/AT]AGTTAATACAATTAT	8850
rs773728961	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20049571	GGGGTAGAGGGGGTC[A/G]CTTTTCTTCCAAATG	8850
rs773744935	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20088690	CTCTTCCATTCCATA[A/G]GTTGTCTCTTTACTC	8850
rs773789128	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20121957	TTGGTTTATTACATA[C/G]CAATAACTAACCAAT	8850
rs773798395	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20087100	TTTTTAAAGGATACA[A/G]AATTACTGCTGGATA	8850
rs773815555	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20094330	TGAGAACTCACTATC[A/G]TGAGAACAGCATGGG	8850
rs773827860	snp	C/T	1.65759e-05	0.00287883	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20095348	TGTGGAATATCTCTT[C/T]ACCTGTGTCCACAAG	8850
rs773844740	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20045020	ATTGGGTTATTTATT[G/T]ATTTATTTTTTTGAG	8850
rs773846019	snp	C/G	1.65143e-05	0.00287348	intron-variant	KAT2B	GRCh38.p7	3:20148334	TTTATTCACCTCATG[C/G]AAATATTTTGAAATG	8850
rs773852620	snp	G/T	5.13027e-05	0.00506445	synonymous-codon, intron-variant, nc-transcript-variant	KAT2B	GRCh38.p7	3:20148471	AGGATATTATGAAGT[G/T]ATAAGGTTCCCCATG	8850
rs773888839	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20112265	CCCACTCTTTGGAAA[C/T]TAGACTGCAAAAGCA	8850
rs773890763	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20098977	GAAAAGGCAGTAAGC[A/G]AGAAAGGAGGGAAAG	8850
rs773908616	snp	A/G	2.82841e-05	0.00376049	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20126098	AAGAATACATCACAC[A/G]GCTCGTCTTTGACCC	8850
rs773965499	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20134366	ACCACCTTGATTATG[A/G]TCTTTTTCACTATCG	8850
rs774024845	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20054318	ATCTTTAGTAGAGAC[A/G]GGGTTTTACCATCTT	8850
rs774058123	snp	A/G	1.68542e-05	0.0029029	intron-variant	KAT2B	GRCh38.p7	3:20095212	TTAAAAATGGGGAAT[A/G]TTTGGTTTCCAATTG	8850
rs774076623	in-del	-/G			intron-variant	KAT2B	GRCh38.p7	3:20102806	TCAGAGGCACATCAA[-/G]CTTGCATTAGGGAGC	8850
rs774079636	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20146546	CCTGCCCGTCTCTGT[A/G]TTATCTCTAGTCTTT	8850
rs774105877	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20075032	GCACTTTGGGAGGCC[A/G]AGGCTGGCAGATCAC	8850
rs774145898	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20132697	CACAGCCCTTTCTCA[C/T]AAGCAACTTGGAATC	8850
rs774152195	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20074983	AAATATAATACCATA[A/G]GGCCGGGCGTGGTGG	8850
rs774160523	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20126425	TTCATAATCAAAATA[C/T]TGGTTTTGGTATCTT	8850
rs774169398	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20145137	ATGAATAAAGCAATG[C/T]AAAATATCTTACACT	8850
rs774173364	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20044546	ACTGCTATCTGTGGC[G/T]CCTTATCGAGGGTTC	8850
rs774181151	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20114534	TAAATATTAGTAACT[C/T]TTATGATGGTAATGA	8850
rs774185147	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20103550	TAGTAGCTGGGACTA[C/T]AGGCACATGCCACCA	8850
rs774192633	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20056918	GGAACATAACATGAT[A/T]TGGACTGCAATTGCC	8850
rs774193696	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20086679	GGGTCCATCACTCTG[C/G]CTTTCAATTACTTTT	8850
rs774206732	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20052212	TAAAGTAGCAGCACC[C/T]CATCTATCACTCTAT	8850
rs774231806	snp	A/C	1.6531e-05	0.00287493	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20146326	TACAGATAATTAAAA[A/C]ACTGATTGAAAGAAA	8850
rs774251405	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20048631	ATACTCCGTGTAGTG[C/T]CAATAAAATTAGGAT	8850
rs774269395	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20139258	TTATGTAATTAGAAA[C/G]CTTTTTGTGCTCTGA	8850
rs774275826	snp	A/C	1.69781e-05	0.00291355	intron-variant	KAT2B	GRCh38.p7	3:20111592	TTGACTTCTCTTGTC[A/C]CAGGTGGCTGTGTTA	8850
rs774293236	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20064645	GGGTAGAATGAGTAA[C/T]CCCAGGCAAGTCTCT	8850
rs774295065	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20087732	ACTTTTTAAGATTCT[A/G]CATACAAATAAGATC	8850
rs774307623	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20149027	ATACTCTTTATTTTA[C/T]GCTTTGTCTCATATC	8850
rs774359585	snp	C/T	3.38238e-05	0.00411227	utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152526	TTAATTGACAAGTGA[C/T]TTTTTTTCCCCTCTG	8850
rs774367100	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20115386	TTCTGGAGTCGCAGT[A/G]ATCCCAGAAAGAGGA	8850
rs774376560	snp	C/T	1.64784e-05	0.00287035	missense, intron-variant, nc-transcript-variant	KAT2B	GRCh38.p7	3:20127440	AACACAAAACCCTTG[C/T]TTTAATTAAAGATGG	8850
rs774419775	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20042823	CATGGGTGAGATGTA[A/G]CACCACTTCCAAGTG	8850
rs774435018	in-del	-/TTTCC	1.65567e-05	0.00287716	intron-variant	KAT2B	GRCh38.p7	3:20148231	CTCCTTGTTTCCCTT[-/TTTCC]TTTCAAGTAAAGAGC	8850
rs774487070	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20068432	GATACCTAATGACCA[A/G]CTCCCACCTTTCTTC	8850
rs774498089	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20134340	CCTTTTCCTCTATTC[A/G]TCTTCTCTTTACCAC	8850
rs774502035	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20065827	ATGCTTAAACTGTTA[C/G]GGTCCATAGTGAAGA	8850
rs774506837	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20056771	GGAGGAGGCACAAGG[C/T]ATTTTAGAATGCCAC	8850
rs774535805	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20150315	CAAGATTGACAAATC[A/C]GTAATTTTACATTTT	8850
rs774544316	snp	C/T	0.000263883	0.0114835	intron-variant	KAT2B	GRCh38.p7	3:20119590	TTCTTCTCCTTTTGC[C/T]GGGGCAGTTATCAAT	8850
rs774546926	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20125183	AAAAAATTAGCTGGG[C/T]GCCGTGGCAGGCTCC	8850
rs774564899	in-del	-/TATA			frameshift-variant, nc-transcript-variant	KAT2B	GRCh38.p7	3:20114908	TGCTAGAAGAAGAAG[-/TATA]TAGTCAAAACTCTCC	8850
rs774565376	in-del	-/AT			intron-variant	KAT2B	GRCh38.p7	3:20075125	AAAAATTAGCTGGGC[-/AT]GGTGGCAAGCACCTA	8850
rs774617444	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20042939	GGGTCTCACTCTGCC[A/G]CGTAGGCTGGAGTGC	8850
rs774642774	snp	C/G	1.64866e-05	0.00287106	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20101408	ATCTGGAGGCACCAT[C/G]TCAACGAAGACTGCG	8850
rs774650619	in-del	-/TTCT			intron-variant	KAT2B	GRCh38.p7	3:20067653	TTTTAGATCCTTGAA[-/TTCT]TTCTTTATTTATTTT	8850
rs774691663	snp	C/T	1.66101e-05	0.0028818	intron-variant	KAT2B	GRCh38.p7	3:20125894	ATTTTTTCCTGTCTC[C/T]TGCATCTCAGACCAA	8850
rs774695733	snp	C/T	1.66217e-05	0.0028828	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20101298	TAAGGGTGTGAATAA[C/T]TTTGTGCAGTACAAA	8850
rs774699311	snp	A/G	1.65261e-05	0.0028745	intron-variant	KAT2B	GRCh38.p7	3:20119561	CCTAAGAAAGGAGTC[A/G]GTCATCTAACACCTT	8850
rs774743242	snp	A/G	1.67621e-05	0.00289495	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20122796	CCTGCAGCAATGCTT[A/G]GACCAGAGGTCAGCA	8850
rs774759565	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20080339	TCTGCCTTAGATCTG[C/G]AAGCTCACACCACCT	8850
rs774797002	in-del	-/C	3.59441e-05	0.00423919	intron-variant	KAT2B	GRCh38.p7	3:20122632	GTTTTGTGTTTAGAA[-/C]CACCCATTGTTTGCC	8850
rs774806913	snp	A/G	1.64844e-05	0.00287087	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20140318	GTGAGCTAAATCCAC[A/G]GATCCCGTACACAGA	8850
rs774833897	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20117682	GGGAATGTCCTTGTT[A/G]ACTGAACTGTGGCTG	8850
rs774857705	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20099789	AGACAGACAGAAACA[A/G]AAGAGAGAGGAGAGA	8850
rs774884336	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20049986	AGGCGGATCGCTTGA[A/G]CTCAGGAGTTCGAGA	8850
rs774892766	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20073616	TTGTTGACTTAATTG[A/G]TATCTCAAACAATGT	8850
rs774900860	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20061171	CCCCTCGGCAACCAC[C/G]ATTCCTATCTCTATG	8850
rs774921997	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20129217	TTTTCTAGTAGTTAT[A/G]TGTATATATTTTTAA	8850
rs774922461	snp	A/T	1.64893e-05	0.0028713	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20111695	TCGCTCGGTCTTCAC[A/T]GTTATGAGGCGACAA	8850
rs774926399	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20112459	ATAGAAAGTTGCAGT[A/G]CTGCACCATTGGCCT	8850
rs774953258	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20084146	CATTTAGACAACTAC[A/G]TATTTATATAGTGTA	8850
rs774973443	snp	C/G			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039570	TTTTTTCCCCTCCTC[C/G]GGCAGATTTGACCCA	8850
rs774973502	snp	A/C/G	9.88507e-05	0.00702969	missense, intron-variant, nc-transcript-variant	KAT2B	GRCh38.p7	3:20127458	TAATTAAAGATGGCC[A/C/G]TGTTATTGGTGGTAT	8850
rs774974747	snp	C/T			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20071201	AATCTGTATATTTTG[C/T]AACTACAGTGCACTT	8850
rs775022480	snp	C/T	1.85081e-05	0.00304199	intron-variant	KAT2B	GRCh38.p7	3:20099832	CCAATTAAGTTTTTC[C/T]TTTTCTTTTTTTTAA	8850
rs775032447	in-del	-/CT			intron-variant	KAT2B	GRCh38.p7	3:20143504	TAAAAATAGAATTAC[-/CT]CATTCCACACAGAAA	8850
rs775076711	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20071958	CAACCTTAGCCTAGA[C/T]CTTAGCTGTGTTTGT	8850
rs775089833	snp	C/T	1.74772e-05	0.00295606	intron-variant	KAT2B	GRCh38.p7	3:20147949	ATTCAGTGTTTCACT[C/T]TGTTGACGTATAGGA	8850
rs775090537	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20142291	TCCAGCCTTCCCTCA[C/T]ACATTCCGTTGAATG	8850
rs775120277	snp	A/G	3.48572e-05	0.00417461	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20136924	AATGTATTTGTTTGT[A/G]TACTAACTTCCACAC	8850
rs775170028	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20046374	ATCACTTGAGCTCAC[A/G]AGTTCGAGACCAGCC	8850
rs775255430	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20065923	CCGCATGTATTATTT[A/G]ACATTTTCTAGTAGT	8850
rs775259983	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20045215	TAGAGATGGGGTTTC[A/G]CCATGTTTGCCAGGC	8850
rs775264860	snp	A/T			utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20154157	CCTGTGAAAGTTTGT[A/T]ATTTTCTGAGTAGAC	8850
rs775274612	snp	A/G			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20038753	GCAGAGCCAGGAGAG[A/G]GTAACACTGGTAACG	8850
rs775303782	snp	A/G	1.77333e-05	0.00297764	intron-variant	KAT2B	GRCh38.p7	3:20148502	GGTAATACCATTAAC[A/G]TTTTCTAAGTATAGA	8850
rs775328554	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20133733	TCAGTGGGTCTCCCA[C/G]TTTACATTTTTCACC	8850
rs775335540	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20076498	AAACCTTTTTCTGAG[A/T]TTACTCTTCCTTCCT	8850
rs775341503	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20094408	GACATGTGGGGATTG[C/T]AATTTGAGATGATGT	8850
rs775350628	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20107842	GAGTTGGAGTCTTGC[C/T]GTGTTTCCCAGGCTG	8850
rs775403639	in-del	-/CCTT			intron-variant	KAT2B	GRCh38.p7	3:20130994	TGAGAAACAGTTCTT[-/CCTT]TAGTTTCCTGGCCTT	8850
rs775421038	snp	C/T	3.30748e-05	0.00406649	intron-variant	KAT2B	GRCh38.p7	3:20148233	CCTTGTTTCCCTTTT[C/T]CCTTTCAAGTAAAGA	8850
rs775435325	in-del	-/ATA			intron-variant	KAT2B	GRCh38.p7	3:20075286	AAGAAAAAAGAAAAT[-/ATA]ATAGTATAAAACTTT	8850
rs775449119	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20075130	TTAGCTGGGCATGGT[A/G]GCAAGCACCTATAAT	8850
rs775504161	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20095156	TATTACCAGTGAACT[C/T]AAAGGATTGATGGTA	8850
rs775504963	snp	C/G	1.76752e-05	0.00297276	intron-variant	KAT2B	GRCh38.p7	3:20111822	GGTCTTTGTTTGATC[C/G]CAGAGCTTGAGGTTG	8850
rs775541059	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20087882	TGGGCTCAAGGGATC[C/T]TCTTGCCTTAGGTTG	8850
rs775628839	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20087022	CCTGACCTCGTGATC[C/T]ACCTGCCTTGGCCTT	8850
rs775636060	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20057221	CCAACAAAGGGAATA[A/G]GGTAGTTGAAAAGGG	8850
rs775645714	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20114801	GAGACGCTGATGTTA[A/G]GGTGATTGTCACAGA	8850
rs775679304	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20084016	GAACAGAAAGTTCAG[C/T]GCTACTTCCTCAGAG	8850
rs775709466	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20126378	ATTCTTTATAGCAGT[A/G]AGAGAATGTAACACT	8850
rs775726050	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20081436	TCACTCTCTGGCACC[C/G]TGGGTGTTTGCAAGT	8850
rs775739443	in-del	-/AGTT			intron-variant	KAT2B	GRCh38.p7	3:20122490	ATGAATTGGGTTGGC[-/AGTT]ATTGTGAGCTCACAA	8850
rs775779116	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20120564	TCCAAAGCAAGTCAC[A/G]TAGTTGAACTCAGAG	8850
rs775794383	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20152236	ATGATAAAAATGTAA[G/T]CAAACCAACAACATA	8850
rs775797331	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20139537	CAGTGAACTGCTGGC[A/G]ATGGTGCTGAAGTTC	8850
rs775827585	in-del	-/ATT			intron-variant	KAT2B	GRCh38.p7	3:20129972	TACCCATTTTTTAAA[-/ATT]ATTATTATTATTATT	8850
rs775851095	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20067970	GCCTGTCCCGTCTGG[C/T]TTAATTTCATTTCTT	8850
rs775863470	snp	C/T	1.64868e-05	0.00287109	stop-gained, nc-transcript-variant	KAT2B	GRCh38.p7	3:20101422	TCTCAACGAAGACTG[C/T]GATCTCCCAATGATG	8850
rs775949909	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20052085	GCATGTGGTTACCTG[C/T]TGCTTTGCACACTTT	8850
rs775950104	snp	C/G	0.00010038	0.00708377	intron-variant	KAT2B	GRCh38.p7	3:20119775	TTGCTCCAGGAGCTC[C/G]ATTACCTGAGGAGTG	8850
rs775954057	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20042312	GCAAAAAAGATGAAG[C/T]GGGGAGTGTGCTTCT	8850
rs775987740	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20090878	CTGAGTAGCTGGGAC[A/T]ACAGGCATGTGACAC	8850
rs776005322	snp	A/G	1.6504e-05	0.00287258	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20119696	AGTCCTGCCTGCAAA[A/G]CCTCTTCTGGACTTG	8850
rs776016330	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20063234	CACTATGTCCAGCTA[A/C]TTTTTAAAATTTTTG	8850
rs776040039	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20051383	TCCCCTGGAGTCCGT[A/T]TTGGTGAGTCCTTAC	8850
rs776048012	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20125229	AGAATGGCATGAACC[C/T]GGGAGGCGGAGCTTG	8850
rs776067737	snp	A/C	0.00182853	0.0301815	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20072368	TAATGGCTGGAAAAA[A/C]CCTAACCCCTCACCC	8850
rs776072965	snp	A/G			synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20119647	ATACAATTCAACCTC[A/G]TCTTCCCTTGAGCAG	8850
rs776088282	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20080418	AGGCTTGACTGCAGA[A/C]CTCTGTAGAGAGAAT	8850
rs776101965	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20092123	AGCCCAGTGCTTTGT[C/T]ATTGATTTTCTGTGT	8850
rs776110594	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20073805	CCTCAGGAAATGTGA[C/T]GTAATAAATGTCTGG	8850
rs776131138	in-del	-/AGA	3.30606e-05	0.00406561	intron-variant	KAT2B	GRCh38.p7	3:20127572	TAAACCCAAGGTCTT[-/AGA]AGAAGAGCAGAATGT	8850
rs776150307	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20121213	TAATATGTAATACTT[C/T]TGGAAGAATCGTCTA	8850
rs776171694	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20042479	GTGATGACTACACCA[A/G]AATCTCACAAATCAC	8850
rs776189626	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20102187	TGGGCATGGTGTCAC[A/G]TGACTGTAATCCTGG	8850
rs776198352	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20114172	TCCAGATGATTTCTA[A/T]GGGTTGCCAAAACTT	8850
rs776208730	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20143656	ATCAAAGGTAGATTG[A/G]ATAAAGAAAATGTAG	8850
rs776218431	in-del	-/TCTTA	1.67615e-05	0.0028949	frameshift-variant, utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152516	GAAGCTGGATTAATT[-/TCTTA]GACAAGTGATTTTTT	8850
rs776232228	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20144941	ACTGGGATTACAGGC[A/G]TGCACTACCATGCCC	8850
rs776236274	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20130609	GACACTTTTAGGGAT[A/C]CTAAAGGGAAACTGA	8850
rs776274872	in-del	-/CTC			intron-variant	KAT2B	GRCh38.p7	3:20066256	TGTCTGTCTCCAAAT[-/CTC]CTTCTTCTTTCTCTT	8850
rs776321993	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20143541	TACTGAGCATATACC[C/T]GAAGGAAAATAAATT	8850
rs776344007	snp	A/G	1.67959e-05	0.00289787	intron-variant	KAT2B	GRCh38.p7	3:20114991	GGCATCCAAACAGGT[A/G]AGTTTCCTTTTACAT	8850
rs776386589	in-del	-/ATGTGTGT			intron-variant	KAT2B	GRCh38.p7	3:20121732	CATACACATATGCAT[-/ATGTGTGT]GTGTGTGTGTGTGTG	8850
rs776389057	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20123509	TTGAATAATTGAGAC[A/G]GGGAATGTGTGGCTT	8850
rs776391286	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20072850	TAATAATGATCATTT[C/T]TATTATTTCTGTTGC	8850
rs776396620	snp	G/T	3.609e-05	0.00424779	intron-variant	KAT2B	GRCh38.p7	3:20111834	ATCCCAGAGCTTGAG[G/T]TTGCTAAATACAATG	8850
rs776397913	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20054460	GTGTGAATAATGTCT[C/G]TAATGGTCCACTTGG	8850
rs776398143	snp	A/G	1.67466e-05	0.00289362	intron-variant	KAT2B	GRCh38.p7	3:20148197	ATCAGCTGGCAATAG[A/G]GTAAAACTCTAATCA	8850
rs776404886	snp	A/G	1.82277e-05	0.00301886	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20137098	TCACTCCTTTTCTTA[A/G]TATGTTCTCAGGTAG	8850
rs776451190	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20135056	CTGTTGAATAGTATA[C/T]CTCTATACACATGTG	8850
rs776455238	in-del	-/TGC			intron-variant	KAT2B	GRCh38.p7	3:20044152	TGTCCTGGTAAAGGT[-/TGC]TTCAGAGTCATTTTG	8850
rs776457966	snp	C/T	1.65436e-05	0.00287602	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	KAT2B, MIR3135A	GRCh38.p7	3:20136968	ACACCTGATGAATCA[C/T]TTGAAAGAATATCAC	8850
rs776479046	snp	A/G			intron-variant, nc-transcript-variant	KAT2B	GRCh38.p7	3:20122946	CCTGGTGGTCAGTGT[A/G]GAGAGGGCAGGAACA	8850
rs776493175	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20131695	ACCTCAGCATTCTGA[A/G]TAGTTGGGATCACAG	8850
rs776493805	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20133821	TAAACGTATTTGCAC[A/G]CCGTCAAGTGCAATA	8850
rs776507831	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20055302	ATTGTTATTTAATGT[A/G]CCAGGTGTTGATTTA	8850
rs776513052	snp	A/G			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039639	AATAGTTTGACAGAA[A/G]GTATTTAAAAAGAGA	8850
rs776517684	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20068318	GTTTAATTTCAACAC[A/G]TCTTTACCCACTGCG	8850
rs776521405	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20109752	TTTATAATTTTTTTC[C/T]GCTACCAAGATCACT	8850
rs776542665	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20117510	ACTCCAGTATGCTTT[C/G]AAATTCAGAAGGCCT	8850
rs776564290	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20096185	AGAGGAGAAATCAAC[A/T]TATTCCAAATTTATT	8850
rs776596621	snp	C/G	1.71252e-05	0.00292614	intron-variant, nc-transcript-variant	KAT2B	GRCh38.p7	3:20122831	AAACCTGGGCAGCCA[C/G]CTGGTAGACCTCTTC	8850
rs776599229	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20059467	TCACGCTTGTAATCC[C/T]AGCACTTTGGGAGGC	8850
rs776636904	snp	C/T	1.65332e-05	0.00287512	stop-gained, nc-transcript-variant	KAT2B	GRCh38.p7	3:20146397	TTTAAAGATGGAGTT[C/T]GACAGATTCCTATAG	8850
rs776641465	snp	A/C/G	3.29664e-05	0.00405984	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20072420	CAGCAAATAATTGTC[A/C/G]GTCTAACAGAATCCT	8850
rs776649331	snp	A/G	1.71593e-05	0.00292905	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20147964	TTGTTGACGTATAGG[A/G]GAGACAGGCTGGAAA	8850
rs776654246	snp	C/T	5.27709e-05	0.00513641	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20095399	ACAAGTTTATTTCTA[C/T]CTATTTAAGGTGAGA	8850
rs776730887	snp	G/T	4.92162e-05	0.00496041	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20040680	CGGCCGAAGGACCGG[G/T]AGGCGGTGGCTCGGC	8850
rs776767562	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20047567	AACCCAGTGTTATGA[C/G]TTCTTCCATCCCCGA	8850
rs776787752	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20076610	ATGAACTGCCTTGGA[C/T]TCAGCACCCAGCTCT	8850
rs776796970	in-del	-/TTT			intron-variant	KAT2B	GRCh38.p7	3:20151028	ATTGTTTTTTTCTTC[-/TTT]AAATGAGAGAACATT	8850
rs776817924	in-del	AGATGCTTCTGA/GGTGCCTT			intron-variant	KAT2B	GRCh38.p7	3:20058485	AAAAAAGGTTTTCAG[AGATGCTTCTGA/GGTGCCTT]TAGTGAATTACCTCA	8850
rs776833916	snp	A/T	5.40916e-05	0.00520028	intron-variant	KAT2B	GRCh38.p7	3:20122628	ATTTGTTTTGTGTTT[A/T]GAACCACCCATTGTT	8850
rs776848012	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20098869	GTCCTTGTAAGACAC[A/C]GTTCAGTGGTGAGAC	8850
rs776873114	snp	C/T	1.92406e-05	0.0031016	intron-variant	KAT2B	GRCh38.p7	3:20040796	GTACGCGCTCGCCGC[C/T]CTCGGACCGCGGATG	8850
rs776883730	snp	C/T	1.66247e-05	0.00288307	intron-variant	KAT2B	GRCh38.p7	3:20146281	GTATCCATAGACTTC[C/T]TTCCCTAAACACATT	8850
rs776924379	snp	A/G	1.64898e-05	0.00287135	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20111677	GTTTGGGAGAACATT[A/G]CTTCGCTCGGTCTTC	8850
rs776981539	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20117360	GGGGAACAGAAGAGT[C/G]TAATCATCTACTTAA	8850
rs776993968	snp	G/T	1.66871e-05	0.00288847	missense, utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152353	AAACCATGAGTGAAC[G/T]CCTCAAGAATAGGTA	8850
rs776996893	snp	A/T	1.80755e-05	0.00300623	intron-variant	KAT2B	GRCh38.p7	3:20148519	TTTCTAAGTATAGAT[A/T]TAAAACTCTGGATGG	8850
rs777011461	snp	C/T	3.31022e-05	0.00406817	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20122728	AGAAACCCCGAGTTA[C/T]GGGGGATATTCCGAT	8850
rs777020899	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20139673	ATTATGGCTTAAAGT[A/G]TGTAAATGAGTATAT	8850
rs777055591	snp	A/T			missense, utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152387	CGTGTCTAAGAAATT[A/T]TTCATGGCAGACTTA	8850
rs777071940	snp	C/T	1.69318e-05	0.00290957	intron-variant	KAT2B	GRCh38.p7	3:20099859	TTAATGATTTCTTTG[C/T]AGCTCTTGAGAAAGT	8850
rs777099126	snp	A/G			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039109	TGACCCACATTGCAT[A/G]TAACAAAAAGTAGGG	8850
rs777102993	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20043849	CCAAAAGGACAGATT[A/G]CTCTACCTTTGCCAC	8850
rs777117863	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20141705	CAGTGTCTGGTGCAT[A/G]GTAGTTACTCATTAA	8850
rs777123262	snp	C/T	2.0112e-05	0.00317106	intron-variant	KAT2B	GRCh38.p7	3:20095415	CTATTTAAGGTGAGA[C/T]TTTAACATTTTAAAA	8850
rs777169352	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20139924	TTTAATTATGTAATT[C/T]AGTACAAAATTAAAC	8850
rs777186006	snp	A/T			missense, utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152392	CTAAGAAATTATTCA[A/T]GGCAGACTTACAGCG	8850
rs777188425	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20106149	CTGTGTTCACATTTT[A/T]AATTTCTGTTCACAG	8850
rs777247394	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20081736	AAATTCAGGTGGAGG[A/C]AAGATTGTAAAAACA	8850
rs777261588	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20084355	TGCTTCAGTGCTCCC[C/G]CTACCACTCCAGACC	8850
rs777263800	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20053318	AGGTGGGCAGATTGC[G/T]TGAGCTCAAGGGTTT	8850
rs777264379	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20104774	TCATTACAGAGCTAA[C/T]TTGTAAATATTTATT	8850
rs777299779	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20109554	AACTCCTGGGCTCAA[A/G]CGATCTTCCTGCTTG	8850
rs777398044	snp	C/T			missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20126079	CAGCTGCCCCGAATG[C/T]CAAAAGAATACATCA	8850
rs777421549	snp	C/T	1.68926e-05	0.0029062	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20040724	AAGAAAGCGCAACTA[C/T]GCTCCGCTCCGCGGG	8850
rs777432304	in-del	-/C			intron-variant	KAT2B	GRCh38.p7	3:20046098	AAAAGAAAAAAGTGT[-/C]CCCAGAATTCCTAGA	8850
rs777435480	snp	G/T	1.65597e-05	0.00287743	intron-variant	KAT2B	GRCh38.p7	3:20140392	TTGACTCCCTTACCT[G/T]CTGTACAGGCCAGTC	8850
rs777440493	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20088966	TGCATGTGGATATCC[A/G]GTTGTCCCAACAGCA	8850
rs777445881	in-del	-/T			intron-variant	KAT2B	GRCh38.p7	3:20083101	TCACTACTGATACAG[-/T]GTACATTGATGCACA	8850
rs777454223	snp	G/T			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20071155	ATAAACATTGTTAAT[G/T]ATGTATTTTATATTT	8850
rs777482348	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20048518	CGGTTGTTAAGTAAA[C/T]CCATAGGGTCTGATC	8850
rs777501635	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20127406	GGTAAAACTTTGACA[A/T]AATCTTATTCTTTCA	8850
rs777526136	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20110239	GGATGATTTGGGTCT[G/T]CTCTGAAGGAATAAG	8850
rs777585016	snp	A/G	1.71003e-05	0.00292401	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20122668	TTTTGATCATCATAG[A/G]AGAAAAGAGGAAAAT	8850
rs777613324	snp	A/T	0.000441422	0.0148498	intron-variant	KAT2B	GRCh38.p7	3:20152298	GGTGTTTAAAGGGAG[A/T]CAAAGATTGCTAATA	8850
rs777613415	snp	A/C	1.65176e-05	0.00287376	intron-variant	KAT2B	GRCh38.p7	3:20127407	GTAAAACTTTGACAT[A/C]ATCTTATTCTTTCAG	8850
rs777627247	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20087657	ACCAGCATCTCTACC[C/T]GTACCTCACGTTCCA	8850
rs777666389	snp	C/G	1.68224e-05	0.00290016	missense, intron-variant, nc-transcript-variant	KAT2B	GRCh38.p7	3:20148446	AACCTGTGAAGAGAA[C/G]AGAAGCTCCAGGATA	8850
rs777719882	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20080135	ATGATACAATGTGAT[A/C]CCATTCTCCTGCTTA	8850
rs777732031	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20121135	AAAATATTGTTACTT[A/G]TCTCCAAAAACAAAC	8850
rs777765617	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20065607	GTCCTTTTTAGCAAA[G/T]CAAGTAACGAGTCCC	8850
rs777768090	snp	A/T			utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152970	TAAGGAAGGGATACA[A/T]GATTTTAAAAAAGCC	8850
rs777808561	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20109246	TTTAACTCTATGGTT[G/T]CATTACTAGTTATTT	8850
rs777813180	snp	C/G	2.00801e-05	0.00316854	intron-variant	KAT2B	GRCh38.p7	3:20099811	GAGGAGAGAGAGATA[C/G]ACATACCAATTAAGT	8850
rs777823557	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20120376	GGGATTACAGGTGCC[C/T]ACCATCATGCCCTGC	8850
rs777838615	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20063821	GCTGGGATTACAGAC[A/G]TGAGCCACCACGCCC	8850
rs777853878	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20151861	ATGTATTTATTATCA[G/T]TTTCTCTATATGACA	8850
rs777868109	snp	A/C	1.65356e-05	0.00287533	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20095315	AGAAATGAACAGACT[A/C]CTGGGAATAGTATTG	8850
rs777887377	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20144445	AGGCACCCGCCACCA[C/T]GCCCAGCTAATTTTT	8850
rs777905172	in-del	-/A			intron-variant	KAT2B	GRCh38.p7	3:20058453	GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	8850
rs777910129	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20131429	GTCTAAGATAAAGAT[G/T]GCTGAGCTCTGCCAA	8850
rs777923094	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20146825	GGTCAGAATTAGAAG[A/C]AGCCCAGTTCTGATG	8850
rs777936328	in-del	-/TT	0.00101956	0.0225553	intron-variant	KAT2B	GRCh38.p7	3:20148037	TGTTAATGGAAGTGA[-/TT]TTTTTTTTTCCCCAC	8850
rs777985994	snp	A/G	1.6566e-05	0.00287797	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20114888	TGTGTCTAGATTTCT[A/G]TCCATGCTAGAAGAA	8850
rs777986437	snp	C/G	0.00102407	0.022605	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20040634	GGCTCGGGCGCCTGC[C/G]GTCCGGCGACGGCAG	8850
rs778010994	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20124859	TCACCAGTTAGGGCC[G/T]TCCTTCCTTGAAGAG	8850
rs778040097	snp	C/T	1.6588e-05	0.00287988	intron-variant	KAT2B	GRCh38.p7	3:20101484	GTAATCAGATGCAAG[C/T]TCTTTTCCTTTGGCC	8850
rs778087139	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20113073	GAGAACCAGTACATG[A/G]GACTAAGTCATGACA	8850
rs778088129	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20102923	TGTAACAGCAGATAA[C/T]ATGGAAGAATTGTAT	8850
rs778090145	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20091772	GTTCAGGAGAATGCT[A/G]TTTAATTTCAACCTA	8850
rs778120598	snp	C/G	1.80059e-05	0.00300043	intron-variant	KAT2B	GRCh38.p7	3:20147919	ATGTTATTCTCTTGA[C/G]CAAAAGCACTTCTCA	8850
rs778121451	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20073497	TTACAGAGCATACAA[A/G]TAGATAATGTGATCT	8850
rs778124471	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20062884	TTTCGTTGTTGTTGT[C/T]GTTGTTGAGTTGTAG	8850
rs778131889	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20046271	CATGGGTACAGGACT[A/C]TAAAATTAGTCTTAA	8850
rs778134232	in-del	-/T/TT	0.308832	0.243371	intron-variant	KAT2B	GRCh38.p7	3:20148036	TGTTAATGGAAGTGA[-/T/TT]TTTTTTTTTTTCCCC	8850
rs778160643	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20123278	CTTCACCCCTAACTA[G/T]TTTTGCATGTACTGT	8850
rs778165184	in-del	-/TTT			intron-variant	KAT2B	GRCh38.p7	3:20079203	ACCACACCTGGCCTC[-/TTT]TTTTTTTTTTTTTTT	8850
rs778172722	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20062752	CAGGCGTGAGTCACC[A/G]TGCCTGGCCCATTTT	8850
rs778236219	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20133215	TTACAGGTAAGAGGT[C/G]ACTGTGTGTTTTGTT	8850
rs778277168	snp	G/T	1.79078e-05	0.00299226	intron-variant	KAT2B	GRCh38.p7	3:20099986	AGCCCTCTTTTTATT[G/T]GCTCAAGGCTGAAGA	8850
rs778293971	snp	A/G	1.64904e-05	0.00287139	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20101387	TAAACCGCATCAACT[A/G]TTGGCATCTGGAGGC	8850
rs778374040	snp	A/C	1.64857e-05	0.00287099	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20126003	TGGCAATTCCCTCAA[A/C]CAGAAACCAAACAAG	8850
rs778400911	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20041698	GCGGGGACTTGGCCT[A/T]GTCAGCTCCTGCGGC	8850
rs778408775	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20055913	ATAGTACATACTGTT[C/G]TTTCACTCAGTATAT	8850
rs778424973	snp	A/C/G			intron-variant	KAT2B	GRCh38.p7	3:20060168	TTCTGCCTTTTGGCT[A/C/G]TCATGAATAATGTTG	8850
rs778429148	snp	A/T	1.64887e-05	0.00287125	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20148274	CCTGACCAGCTTTAC[A/T]GCACGCTCAAGAGCA	8850
rs778429289	snp	G/T	1.66532e-05	0.00288554	intron-variant	KAT2B	GRCh38.p7	3:20125888	TGTGTAATTTTTTCC[G/T]GTCTCTTGCATCTCA	8850
rs778432596	snp	A/G	1.66123e-05	0.00288199	intron-variant	KAT2B	GRCh38.p7	3:20119755	GGATAAGAGAGGGCT[A/G]TGACTTGCTCCAGGA	8850
rs778450398	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20149401	CTTGGGAGGCTGAGG[C/T]TGGAGGATCACTTGA	8850
rs778483303	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20076339	AAAAAATATTTCCCC[C/G]TACTCCTTCCTTTCT	8850
rs778502914	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20055186	GGTTTGAACCCTGAT[A/G]TGTGACTATGGGGAG	8850
rs778573481	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20089351	AGTATTAATTCTTCC[A/T]ATCTGTGAACATAAA	8850
rs778576070	snp	A/C	1.67374e-05	0.00289282	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20122689	AGAGGAAAATGACTG[A/C]TTCTCATGTTCTGGA	8850
rs778580377	snp	A/G			downstream-variant-500B	KAT2B	GRCh38.p7	3:20154544	TTTCATAAAAAATCC[A/G]TAGGTCATCAGTAAG	8850
rs778592506	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20078407	CACCTTTTTCTTTCT[C/G]TTCTGTCCAGGCTGA	8850
rs778601931	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20060276	TCATGTGGTAAATTT[A/T]TGTTTAACTTTTTGA	8850
rs778619954	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20049751	GCCCAGGACAGACAT[A/T]TACATGCTCTTGATT	8850
rs778625185	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20078665	ATTACAGCTACCGCA[A/C]CCTTCATCATCTTTT	8850
rs778644918	in-del	-/C			intron-variant	KAT2B	GRCh38.p7	3:20074585	TATCAGGGTTCTTTT[-/C]ACTTCACACAGCAGA	8850
rs778693926	snp	A/G	1.79255e-05	0.00299373	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20136912	TCTCCCCAGTCTAAT[A/G]TATTTGTTTGTATAC	8850
rs778713786	snp	C/T					GRCh38.p7	3:20049322	TTTATTTGTAAAAAA[C/T]GTTCCATTGGTATTA	8850
rs778728754	in-del	-/AG					GRCh38.p7	3:20099761	GTGTGTGTGTGTAAG[-/AG]AGAGAGAGAGAGAGA	8850
rs778733965	snp	C/G					GRCh38.p7	3:20117307	TCAGAAGTGGGCTGT[C/G]TTCTCTTGTTCTACT	8850
rs778748599	snp	A/C	1.6941e-05	0.00291036			GRCh38.p7	3:20111785	CCTCACTCATTTCCC[A/C]AAGTAAGGGAGAGTT	8850
rs778773213	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20099413	ATCTTGGTCTCTCAC[A/G]TCTTTAAATAAGATC	8850
rs778807206	in-del	-/A	1.66156e-05	0.00288228	intron-variant	KAT2B	GRCh38.p7	3:20095259	CTTTGATCTTATCAT[-/A]AAGCTGCTCATGTTT	8850
rs778821928	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20128645	GACAGAAAGAGCTCT[C/T]ATCTATACCTTGTCC	8850
rs778831265	in-del	-/A			intron-variant	KAT2B	GRCh38.p7	3:20119792	TTACCTGAGGAGTGC[-/A]AAAGGTAGACTTGAA	8850
rs778860966	snp	A/G	4.9516e-05	0.00497549	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20111648	AGTCTACCTCGGTAC[A/G]AAACCACACAGGTGT	8850
rs778875846	snp	A/G			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070206	GGTTAGGTATTCCAG[A/G]TTCACATGGCCCACT	8850
rs778878329	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20046548	AGATCATGCCACTGC[A/C]CTAGACCTTGTCTCA	8850
rs778915280	in-del	-/TTTTCT			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20069520	TTTCTTTTTCTTTTC[-/TTTTCT]TTTCTTTTTTTTTTT	8850
rs778932303	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20127873	GCATAGTTCACAATG[G/T]GGTTTGCACTCCTAT	8850
rs778947538	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20121209	TAAATAATATGTAAT[A/G]CTTCTGGAAGAATCG	8850
rs778948873	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20110555	GTGCATGCCTGTGGT[C/T]CCAGTTGTTTGGCAG	8850
rs778976740	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20141060	GTCCATTAGCCACCC[C/T]GTTCACTCAGCACAC	8850
rs779027526	snp	C/G			utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20153189	TGATAATTCTGTCTA[C/G]TTACAACAAACTTGT	8850
rs779039411	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20132894	ATGGTGCATACAACA[A/G]TCTCTCTTGCATCGA	8850
rs779045431	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20127965	CCTGCCACTCACCTC[A/G]TGCTGTGCAGCCCGG	8850
rs779137479	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20055739	ATCTTTAGTTCTGAT[A/C]CGTTTCAACAAATAC	8850
rs779180298	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20065143	TTGGGATGAAAACAT[C/T]ATCCCAGTCCTGTTG	8850
rs779188811	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20054053	TCCATCCTCCTCGGC[C/T]TCCCAAAGTGCTGGG	8850
rs779197480	snp	C/T	1.9187e-05	0.00309728	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20040748	CCGCGGGCCAAGAAA[C/T]TGGAGAAACTCGGAG	8850
rs779198091	snp	C/G	6.66433e-05	0.00577211	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20126027	AAACAAGAAGATCCT[C/G]ATGTGGCTGGTTGGC	8850
rs779226188	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20102177	AAAAATTAACTGGGC[A/G]TGGTGTCACGTGACT	8850
rs779226862	snp	A/C	1.80023e-05	0.00300014	intron-variant	KAT2B	GRCh38.p7	3:20148048	GTGATTTTTTTTTTT[A/C]CCCACCAAGCAACTT	8850
rs779234626	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20081220	CAGAGGAGCAGGGAC[A/G]TGTTAGCTGCCTGCC	8850
rs779254313	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20147700	CCCACAGTACTGTAC[A/G]TATTTATTTTTTATG	8850
rs779267982	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20051941	TAAATTCCATGGGCT[G/T]CTTTGGAAGATTTCT	8850
rs779285255	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20072800	CTGAGGGTCTTTGAC[C/T]TCAGGGTTGAAACCT	8850
rs779288317	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20125017	AACTGTTCTTTAAAA[A/G]GAGGTGTTAAGAATA	8850
rs779307344	snp	A/C/T	6.63475e-05	0.00575934	intron-variant	KAT2B	GRCh38.p7	3:20140406	TTCTGTACAGGCCAG[A/C/T]CTTAGCTGGGGTGGG	8850
rs779307893	in-del	-/TG			intron-variant	KAT2B	GRCh38.p7	3:20128036	GGACCTCTGTCTCAC[-/TG]TGAGTGTATGTGTAT	8850
rs779312421	in-del	-/CTT			intron-variant	KAT2B	GRCh38.p7	3:20088735	TTTCCTATATAGAAG[-/CTT]TTTAGTTTGATGCAA	8850
rs779317047	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20132086	CCTGTAATCTAAAAA[C/T]AATTTGGGCCAGGCG	8850
rs779324378	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20092758	CTAGGCTGGAGTGCA[C/T]TGGTGTGATGTCGGC	8850
rs779350464	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20086307	AGGAAGAAAAACAAG[C/T]TGTATTGGAGTCTGG	8850
rs779398366	in-del	-/A			intron-variant	KAT2B	GRCh38.p7	3:20094071	GATGAAACAATATTT[-/A]AGTCTGTCTGAGACT	8850
rs779420979	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20125565	AGCAGAAGAAGGAGT[A/T]GTTGTGACAAACACC	8850
rs779454134	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20145422	AGTATTTACCAGCTA[A/T]ATGTTTGAAATCAAT	8850
rs779490955	in-del	-/GTAA			intron-variant	KAT2B	GRCh38.p7	3:20048143	CTTCTCTAAAATGCG[-/GTAA]GTGTCATAAAGCCAA	8850
rs779572932	snp	A/T	1.66241e-05	0.00288302	intron-variant	KAT2B	GRCh38.p7	3:20127381	AAAGTATATTTATAT[A/T]ACTAGGATAGGTAAA	8850
rs779579225	snp	C/G	4.98451e-05	0.004992	intron-variant	KAT2B	GRCh38.p7	3:20101492	ATGCAAGTTCTTTTC[C/G]TTTGGCCCCATAAAG	8850
rs779618348	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20084986	GTTTCATATTATGGA[A/G]CATCTGAAGGAATTT	8850
rs779653126	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20047283	CGCCATGTTTAACAG[G/T]CTGGTCTTGAACTCC	8850
rs779660415	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20041544	CTCCATGCCAGTTTA[C/G]GCACCCTGTCACCTC	8850
rs779680888	snp	C/G			downstream-variant-500B	KAT2B	GRCh38.p7	3:20154827	ATCCTTTTGGGGTTT[C/G]AGAGGACCCAACCAA	8850
rs779693044	in-del	-/TTTC			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20069526	TTTCTTTTCTTTTCT[-/TTTC]TTTTTTTTTTTTTTG	8850
rs779697857	snp	A/G	1.65608e-05	0.00287752	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20122772	GAGGTTATGTCTACC[A/G]TCACGGACCCTGCAG	8850
rs779703942	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20081102	TTGACAGATTTCATT[G/T]TAGTCATTAATTTTA	8850
rs779725220	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20063212	GGCTGTGACTGCAGG[C/T]GTGCACCACTATGTC	8850
rs779726832	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20135001	AACTGGACTAGTCTC[A/G]TATCAATTGCTCAGT	8850
rs779731612	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20068663	GAGCAGAATCTTTGT[A/T]TCATAGTCAATAGTA	8850
rs779765572	snp	G/T	1.65345e-05	0.00287524	missense, utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152447	CAACCCCCCTGAGAG[G/T]GAATACTACAAATGT	8850
rs779811352	snp	C/G	1.65367e-05	0.00287543	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20114930	TCAAAACTCTCCCAT[C/G]TGGGATCAGGATTTT	8850
rs779818532	snp	C/T	1.69726e-05	0.00291308	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152334	TTTTCCTGTGCAGAT[C/T]TGAAAACCATGAGTG	8850
rs779827145	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20055265	CAGTGATATATGTCA[A/G]CTTTTTCCGTTTACT	8850
rs779856448	snp	C/T	1.76993e-05	0.00297478	intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20137086	AACACTGTTTTGTCA[C/T]TCCTTTTCTTAATAT	8850
rs779867237	snp	C/T	1.64806e-05	0.00287054	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20072402	CCCCCCAGAGCCGAC[C/T]TGCAGCAAATAATTG	8850
rs779930508	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20090261	GTGGCAAGGGTGGGT[A/G]TATTTTTCTTGTTCT	8850
rs779935577	snp	C/T	1.64882e-05	0.00287121	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20119605	CGGGGCAGTTATCAA[C/T]CCACCTCCTGTGGCT	8850
rs779935930	snp	C/T			upstream-variant-2KB	KAT2B	GRCh38.p7	3:20039422	TTATAGAACCACCAC[C/T]CAGAAACGAATCCTG	8850
rs779952720	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20117032	CAGTGGGGGACCAAA[A/G]TTATTCAGCAGGATC	8850
rs779963362	in-del	-/AT	1.64871e-05	0.00287111	frameshift-variant, nc-transcript-variant	KAT2B	GRCh38.p7	3:20101434	TGCGATCTCCCAATG[-/AT]ATGATATTTCTGGAT	8850
rs779980305	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20105674	TGGTGGCATGAGCCT[A/G]TGGTCCCAGCGACTC	8850
rs780022721	in-del	-/T	0.00432171	0.0462837	intron-variant	KAT2B	GRCh38.p7	3:20148037	TGTTAATGGAAGTGA[-/T]TTTTTTTTTTCCCCA	8850
rs780068967	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20140641	GATTACAGGTGTGTG[C/T]TACCATGCCCAGCCA	8850
rs780072771	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20128719	GTCCTTAGAATGTTA[C/T]TCATTTAGGGCTGGG	8850
rs780092721	snp	A/G	1.65625e-05	0.00287766	intron-variant	KAT2B	GRCh38.p7	3:20127394	ATAACTAGGATAGGT[A/G]AAACTTTGACATAAT	8850
rs780125313	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20087938	AGCCACCATACCTAG[C/G]TAATTAAAAAAAAAT	8850
rs780135296	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20142726	TGTTTTGAACTGGGC[A/G]GCCTGGTGATGAAAT	8850
rs780160838	snp	C/T			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20070636	TTACACATATATACA[C/T]ACTTCAGAAATGATC	8850
rs780215258	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20060376	GGAGGCCAAGGCGGG[C/T]GGATCACCTGAGGTC	8850
rs780217674	in-del	-/TT			intron-variant	KAT2B	GRCh38.p7	3:20089401	CGTGTCTTCTTCACT[-/TT]TTTTTTTTTTTTTTT	8850
rs780262356	snp	A/G	1.66565e-05	0.00288583	missense, intron-variant, nc-transcript-variant	KAT2B	GRCh38.p7	3:20148403	TTTTCTTTACCCAAG[A/G]GCCATCAAAGCGCTT	8850
rs780263030	snp	C/G	1.91057e-05	0.00309071	intron-variant	KAT2B	GRCh38.p7	3:20040786	CGCCTGCAAGGTACG[C/G]GCTCGCCGCTCTCGG	8850
rs780301580	snp	C/T	1.64825e-05	0.00287071	intron-variant	KAT2B	GRCh38.p7	3:20072319	TTTTGTCTCTTTCTT[C/T]ATTCCATTTTTAGGC	8850
rs780331317	snp	C/T	1.89705e-05	0.00307975	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20126057	CCTACAGAACGTTTT[C/T]TCCCACCAGCTGCCC	8850
rs780334007	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20043772	ATTGGGTACGAGGGA[A/G]TGTAAGAGAGCAAAA	8850
rs780379672	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20092850	AGAACTACAGGCACG[C/T]ACCACCATGCCCAGC	8850
rs780400504	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20065282	TTGCTAGCTGCTACA[A/G]TAATTGGCTTGGCAG	8850
rs780413341	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20128154	ACTGTACAAGTTCAA[C/T]ATGTAACTCAAGTGT	8850
rs780446583	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20122305	TTCAATCCATTTTGA[C/T]GTTTTGGTGTCATAT	8850
rs780458718	snp	C/T	1.6609e-05	0.0028817	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20122711	TGTTCTGGAGGAGGC[C/T]AAGAAACCCCGAGTT	8850
rs780474573	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20093750	TTAATCTTCAAGCAT[G/T]TTTAAGCCAGCACAC	8850
rs780498888	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20066711	TGGCTGGGACATGAA[A/C]TTTAGGGCACACACT	8850
rs780542825	in-del	-/GTTT			intron-variant	KAT2B	GRCh38.p7	3:20056014	TGTATGGACGTACTA[-/GTTT]GTTTATCTGTTGACT	8850
rs780579292	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20116002	AAACCAAAGTACTAG[C/T]GAATGAGGAATTTTA	8850
rs780579364	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20103412	TTTTGTTTTATTTTT[A/G]TTTTTATTTTTTTTA	8850
rs780607954	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20149809	CTGATTTGGGAATCA[A/G]TATTGTCCACTATGT	8850
rs780640772	snp	C/T	1.65042e-05	0.0028726	intron-variant	KAT2B	GRCh38.p7	3:20072284	GTAAAACCATCAGTC[C/T]ACGGCTGCCTGTTAA	8850
rs780667078	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20114791	TTGAAGGTTTGAGAC[A/G]CTGATGTTAAGGTGA	8850
rs780714520	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20146074	CTGTGTGTTTTCTCA[A/G]TATTGGCTTTTCTGG	8850
rs780739619	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20124505	ATAACTCATTCATCA[A/G]CAAGGGGATGGTGCT	8850
rs780741800	snp	C/T	3.3134e-05	0.00407012	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	KAT2B	GRCh38.p7	3:20152471	CAAATGTGCCAATAT[C/T]CTGGAGAAATTCTTC	8850
rs780770589	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20074903	GGTCCTTTCCCAAAT[A/G]CAGGATGCTGACTCA	8850
rs780782344	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20056337	GGTTTTTGGCCTGAG[C/T]AACTGAATGGATGGT	8850
rs780795633	in-del	-/G			intron-variant	KAT2B	GRCh38.p7	3:20043937	ATAAGGTAGTTCACT[-/G]GGGGGGCTTTTGAAA	8850
rs780829414	snp	G/T			intron-variant, downstream-variant-500B	KAT2B, MIR3135A	GRCh38.p7	3:20137722	AGACAGGGTTTTGTC[G/T]TGTTACCCAGGCTGG	8850
rs780838303	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20125743	ATAACTTGTATGTGT[A/G]TGTGTCTCTGTGTGT	8850
rs780848746	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20065459	AAGAACAGTGGCCAG[G/T]CCTGAACATTGGAAT	8850
rs780893087	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20042627	AACTGTCTCAACTCA[A/G]TGTTTCTGTTCTGGC	8850
rs780897947	snp	G/T			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20069883	AAAGTTGTATATTTC[G/T]GTTTGCCATATTCTC	8850
rs780920831	snp	C/T	1.6604e-05	0.00288127	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20140228	CTTTTCAGGGTTTCT[C/T]CAAAGAAATTAAAAT	8850
rs780930414	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20138945	GTCACCAAGGCTGGA[A/G]TGCTGTGGCATGATC	8850
rs780955809	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20086429	CATGGTGAAACTTTG[C/T]GCCAACGGAAAATAC	8850
rs781024946	snp	A/G	1.64893e-05	0.0028713	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20148296	TCAAGAGCATCCTCC[A/G]GCAGGTGAAGGTGGG	8850
rs781033613	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20112400	AGCTCCAAGGCATAA[A/G]TGATCATTTAAATAT	8850
rs781036971	in-del	-/C			intron-variant	KAT2B	GRCh38.p7	3:20150790	CATTTTAGGCTCTCT[-/C]CATCTTTTCTTACCC	8850
rs781041414	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20097376	TTAAAATAACAGTGC[A/G]AATATATTTGCTTGT	8850
rs781087719	snp	C/T	1.65652e-05	0.0028779	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20095270	ATCATAAGCTGCTCA[C/T]GTTTCCCACCTGGAG	8850
rs781113807	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20111046	AGGCATTTTAAATAA[A/C]TCTTACATTTTACTC	8850
rs781129104	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20131287	CCCAAAGTGCTGGGA[C/T]TACAGTTGTGAGCCA	8850
rs781180091	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20041964	TGCTCTTTTTCCACA[C/T]CATATGCTCAGGTTT	8850
rs781203335	snp	A/T			intron-variant	KAT2B	GRCh38.p7	3:20151100	GAGATTTGATGAGTC[A/T]TTGTGTTTCTTAGCG	8850
rs781226491	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20100498	TAGGTGTTGTCAGTA[C/T]CTCTCATTAGCATCA	8850
rs781238082	snp	A/G	1.65718e-05	0.00287848	intron-variant	KAT2B	GRCh38.p7	3:20119735	CCAGGTAAGCTCTTA[A/G]GAGGGGATAAGAGAG	8850
rs781249434	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20091697	TATTGTATTTCCACT[C/T]CTGTTTGTCTTAAGA	8850
rs781292946	snp	G/T	9.93098e-05	0.00704592	intron-variant	KAT2B	GRCh38.p7	3:20140386	AGGTGGTTGACTCCC[G/T]TACCTTCTGTACAGG	8850
rs781294913	snp	C/T	1.64874e-05	0.00287113	missense, nc-transcript-variant	KAT2B	GRCh38.p7	3:20119609	GCAGTTATCAATCCA[C/T]CTCCTGTGGCTGGGA	8850
rs781304334	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20143087	GACTGGGTGATGTAT[C/T]GGAGATGGGGAACTA	8850
rs781356511	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20050970	CTTTGAGAGGCCGAG[A/G]TGGGCAGATCGCTTG	8850
rs781373205	snp	C/G	1.67598e-05	0.00289476	intron-variant	KAT2B	GRCh38.p7	3:20114863	TTTTTAATCTTATTG[C/G]TATTACTCTTGTGTC	8850
rs781490524	in-del	-/TTCT/TTT			intron-variant	KAT2B	GRCh38.p7	3:20139221	ACCCAGCCAGACTTC[-/TTCT/TTT]TTTTTTTTTAAAAAT	8850
rs781494522	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20088342	TATCCATATGGTTTA[C/T]CATACTGGCTGTACT	8850
rs781503012	snp	A/G	8.51665e-05	0.00652503	intron-variant	KAT2B	GRCh38.p7	3:20148012	AAGGTAAGTATGACG[A/G]GCAAGAGGATGTTAA	8850
rs781543067	snp	A/G	0.0002653	0.0115143	intron-variant	KAT2B	GRCh38.p7	3:20072506	CGAGTTCATTGTAGC[A/G]TGAGACTCTTAACTT	8850
rs781565526	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20045841	TACCCGCCTCATGGC[A/G]TAACAGTGAGGATTT	8850
rs781644336	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20054943	AAGCCACAAGGAGCC[A/C]TTTTCTTGTTGAGGA	8850
rs781681560	snp	A/G			intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20135768	GACTGGGAAAGTACG[A/G]ATGGGCATGTGTGAG	8850
rs781690402	snp	C/T	1.66421e-05	0.00288458	synonymous-codon, nc-transcript-variant	KAT2B	GRCh38.p7	3:20122783	TACCATCACGGACCC[C/T]GCAGCAATGCTTGGA	8850
rs781753299	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20059908	TGTTCCTACCCCCCA[C/T]CCCAGATGACCACTA	8850
rs781769207	in-del	-/TATTT			intron-variant	KAT2B	GRCh38.p7	3:20078351	TTTGTCTAGTAATAA[-/TATTT]TAGTTTAGAGGTTTT	8850
rs796068467	in-del	-/AG			intron-variant	KAT2B	GRCh38.p7	3:20142569	GTAGTTGTCATTAGT[-/AG]AGAGAGAGAGAGAAA	8850
rs796080833	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20053527	GTGACAGAGTGAGAC[C/T]CTGTCTCAAAAAACA	8850
rs796086486	in-del	AT/CAAA			intron-variant	KAT2B	GRCh38.p7	3:20073720	ACCTTTTTAAAAAAA[AT/CAAA]AATAAATAAAACAGA	8850
rs796089048	in-del	-/A			intron-variant	KAT2B	GRCh38.p7	3:20096466	AGAAGGAATAACCTT[-/A]AAAAAAAATAAACCT	8850
rs796104160	in-del	-/TAT			intron-variant	KAT2B	GRCh38.p7	3:20062416	ATATTATATATTATA[-/TAT]TATTATATATAATAT	8850
rs796158842	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20060909	ATGATCATGCCACTG[C/T]ACTCCTGGGCAACAG	8850
rs796176819	in-del	-/AG			intron-variant	KAT2B	GRCh38.p7	3:20096950	AAAGAATAATAGGAA[-/AG]AGAGAGAGAGAGAGA	8850
rs796197019	in-del	-/T			intron-variant	KAT2B	GRCh38.p7	3:20120224	CATTCTTTTTTTTTT[-/T]CCTTTTCTTTTCTTT	8850
rs796199418	in-del	-/A			intron-variant	KAT2B	GRCh38.p7	3:20059435	AAAAAAAAAAAAAAA[-/A]GGCCAGGCGTGGTGC	8850
rs796275318	snp	A/C			intron-variant	KAT2B	GRCh38.p7	3:20094616	TCACAAAACTATAGT[A/C]AGACAACAGAACAAA	8850
rs796394882	in-del	-/T			intron-variant	KAT2B	GRCh38.p7	3:20114536	AATATTAGTAACTTT[-/T]ATGATGGTAATGACA	8850
rs796397176	in-del	-/T			intron-variant	KAT2B	GRCh38.p7	3:20120213	ACTTCTGCCACATTC[-/T]TTTTTTTTTTTCCTT	8850
rs796405249	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20049772	GCTCTTGATTGTTTT[A/G]AAGTTGACAATCAAG	8850
rs796505789	multinucleotide-polymorphism	AAA/TTT			intron-variant	KAT2B	GRCh38.p7	3:20085199	ATGTCTATTAATTTA[AAA/TTT]AAAAAGTTTATAAGA	8850
rs796515283	in-del	-/AG			intron-variant	KAT2B	GRCh38.p7	3:20099759	GTGTGTGTGTGTGTA[-/AG]AGAGAGAGAGAGAGA	8850
rs796521880	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20147009	GTAGTTTTCCTAAGG[A/G]TTCTTGTCTGTATGT	8850
rs796534993	in-del	AT/C			intron-variant	KAT2B	GRCh38.p7	3:20139235	CTTTTTTTTTAAAAA[AT/C]TGTTCTTATGTAATT	8850
rs796556696	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20091918	AATACTTTCCTACCA[A/G]TGTGGTTGGAATAGA	8850
rs796612600	snp	G/T			intron-variant	KAT2B	GRCh38.p7	3:20048510	TAATTCTGCGGTTGT[G/T]AAGTAAATCCATAGG	8850
rs796640091	in-del	-/T			intron-variant	KAT2B	GRCh38.p7	3:20112167	AAGAGCTCAAGTGGC[-/T]TTTTTTTTTTTTTCC	8850
rs796727176	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20057566	TCCACTGTGTCGAAG[C/T]CTGAGCTGACTGCTC	8850
rs796738631	in-del	-/C			intron-variant	KAT2B	GRCh38.p7	3:20134033	CAACTACACCCCCCC[-/C]TCACTTGTCATTTGT	8850
rs796793473	in-del	-/AA			intron-variant	KAT2B	GRCh38.p7	3:20105801	GCACGACCCTGTCTG[-/AA]AAAAAAAAAAAAAAA	8850
rs796814780	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20063528	CAGCAACTTCTGAGT[A/G]GGCCTCTTTTTTTTT	8850
rs796834940	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20110868	TCCTCCTCCAGCGTC[A/G]TGCAGTGATGCTGAG	8850
rs796854886	in-del	-/TTTTTTTTTTT			intron-variant	KAT2B	GRCh38.p7	3:20131011	TTTAGTTTCCTGGCC[-/TTTTTTTTTTT]TTTTTTTTTTTGAGA	8850
rs796882439	snp	C/T			intron-variant	KAT2B	GRCh38.p7	3:20118941	AATGTAACATTGATA[C/T]AGTATAGTTACCTAA	8850
rs796935467	in-del	ATA/TG			intron-variant	KAT2B	GRCh38.p7	3:20107367	CAATATATAAAAAAT[ATA/TG]CATTTCAGCTGGGAG	8850
rs796950685	snp	A/G			intron-variant	KAT2B	GRCh38.p7	3:20150336	TTTACATTTTCCCAC[A/G]ATTTCCTTATTTGAT	8850
rs796973527	snp	A/G			intron-variant, upstream-variant-2KB	KAT2B	GRCh38.p7	3:20069565	GAGTCTCACTCTGTC[A/G]CTCAGGCTGGAGTGC	8850
rs796988791	in-del	-/A			intron-variant, upstream-variant-2KB	KAT2B, MIR3135A	GRCh38.p7	3:20135654	GCAAGACTCCATCTC[-/A]AAAAAAAAAAAATAA	8850
rs796995109	snp	C/G			intron-variant	KAT2B	GRCh38.p7	3:20080645	CATATATTTGCAGAG[C/G]AGCTTTCAAAGTTTA	8850

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