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

KMT2A

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs111680	snp	A/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118447986	AGTCCTGCCTACATA[A/T]GTATAAAATGACCTC	4297
rs111681	snp	A/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118447988	TCCTGCCTACATATG[A/T]ATAAAATGACCTCTT	4297
rs125315	snp	C/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118441562	GTTATTTTCAGTCTA[C/G]GTGGTATATTCCTGT	4297
rs471239	snp	C/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118449309	acaactgtaatacca[C/G]cactgtgggaggctg	4297
rs471380	snp	A/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118453272	agctatttcagaggc[A/T]tcatggggataaaag	4297
rs471406	snp	C/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118453270	ctatttcagaggcat[C/T]atggggataaaagcc	4297
rs472368	snp	A/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118453140	atcaggtagcagcta[A/G]aggtggacgtggggt	4297
rs474155	snp	A/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118468058	TGGAAAGGACAAAAA[A/G]CAAAAGCTTCTGCTT	4297
rs474257	snp	C/T	0.00676609	0.0577691	intron-variant	KMT2A	GRCh38.p7	11:118468021	AATTTTAACCTGCTC[C/T]ATAAAAAAAAAAAGG	4297
rs475993	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118452761	ctgtaatcccagcta[A/C]ttgggaggctgaggc	4297
rs476767	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118452690	gccgagatggcgcca[A/C]tgcactccagcctgg	4297
rs476793	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118452685	gatggcgccactgca[A/C]tccagcctgggcagt	4297
rs476868	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118452654	agagtgagactccat[C/T]tcaaaaaTTTTACCA	4297
rs477101	snp	A/G	0.00755907	0.0610114	intron-variant	KMT2A	GRCh38.p7	11:118492703	AAAAGAAGAAGAACC[A/G]CATGGATCACTTTAC	4297
rs477106	snp	A/C	0.4661	0.125701	intron-variant	KMT2A	GRCh38.p7	11:118492709	AGAAGAACCGCATGG[A/C]TCACTTTACCTCAGA	4297
rs477901	snp	C/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118449137	AATGTGGGCTTCTCA[C/G]AATGTGATGGCAAAC	4297
rs478056	snp	C/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118467585	ACAAATTAGCAGGTT[C/T]ATCTCTTAAATTTAA	4297
rs478923	snp	A/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118469752	GCTGTTTCTGCTTTT[A/T]GACATTGACTTAGCT	4297
rs480925	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118444300	CAAACATTGTCCCTA[A/G]ATTATTGCCCTTAAT	4297
rs487396	snp	A/C	0.104938	0.20361	intron-variant	KMT2A	GRCh38.p7	11:118463423	ATGCATTTCACAAAG[A/C]CATCTGGGGATTTCC	4297
rs488696	snp	C/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118442807	CCTGGAAACTAAAGT[C/T]AAACTACTTTTTCCA	4297
rs490330	snp	C/G	0.225766	0.248823	intron-variant	KMT2A	GRCh38.p7	11:118506821	ATGTAACAAAATGTA[C/G]TTCCATCCATGGGCA	4297
rs490946	snp	A/C	0	0	intron-variant	KMT2A	GRCh38.p7	11:118509377	ATGTACTGGAAGAAC[A/C]CTGCACCGAGAGACA	4297
rs490968	snp	A/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118509365	AACACTGCACCGAGA[A/G]ACAGGTGCGCCAAGT	4297
rs492927	snp	A/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118463421	TGGGAAATCCCCAGA[A/T]GTCTTTGTGAAATGC	4297
rs493699	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118486324	GGAAGGATTCACACC[A/C]AAATATTAAAAGTGT	4297
rs493992	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118456332	aaaGGTTCATttttt[A/T]aatttttagtagaga	4297
rs495132	snp	C/T	0.412917	0.189626	intron-variant	KMT2A	GRCh38.p7	11:118465212	tttcactctgtcacc[C/T]agctatagtgcagtg	4297
rs496223	snp	G/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118486537	TGGCAGATACCTCTT[G/T]GGCTTATTACTTACC	4297
rs497209	snp	A/C	0	0	intron-variant	KMT2A	GRCh38.p7	11:118464949	tactacaaaaatgcc[A/C]aggaaagcttcacca	4297
rs497242	snp	C/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118464939	ttcctgggcattttt[C/G]tactaaagctttggt	4297
rs497478	snp	C/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118444324	ATCCACAAGGTTTTA[C/G]TGCTTATAATTAAAG	4297
rs498268	snp	A/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118444256	AAGTGGTCAATCCTC[A/G]TGGATGGACAGAAGT	4297
rs498362	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118444230	GAAGTTGAATATGGG[C/G]ATGTGTAAATATTTC	4297
rs498684	snp	A/G	0.485255	0.0845871	intron-variant	KMT2A	GRCh38.p7	11:118446245	tcccagctacttggg[A/G]ggctgaggcatgaga	4297
rs499189	snp	A/T	0.384401	0.210799	intron-variant	KMT2A	GRCh38.p7	11:118486899	attttttaaattttt[A/T]aaaatttttttgaga	4297
rs500041	snp	C/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118474436	ctgcaaataccactg[C/G]ctccaccatactttt	4297
rs500043	snp	C/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118509345	TTGGCCCACATTGGA[C/T]TGAAACTTGGCGCAC	4297
rs500084	snp	C/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118458876	GAACTAACAAAATTA[C/T]TGAGAACAACTAAAG	4297
rs500839	snp	A/T	0.0198	0.0975087	intron-variant	KMT2A	GRCh38.p7	11:118509393	GTTCTTCCAGTACAT[A/T]TTGTGTGATCACCTG	4297
rs502935	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118478740	ATGCATGAACATATT[C/T]TAAGAGAGAGTGAGA	4297
rs503076	snp	G/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118478692	CAAGGTATCTCCAAT[G/T]TTTCCTGAATTGTCA	4297
rs503106	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118478678	TGTTTCCTGAATTGT[C/T]ATAATTTTGTTGGGT	4297
rs503691	snp	C/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118461928	TGCTGCAAAAAAGTC[C/T]TCCTTTCACTGCACT	4297
rs503782	snp	C/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118461892	GAGCAACAGGCTTCT[C/G]ATCTTGCTCCATCAC	4297
rs507291	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118478988	atagtaggtatatat[A/T]tttatggtatacata	4297
rs514924	snp	C/T	0.409382	0.192607	intron-variant	KMT2A	GRCh38.p7	11:118476148	GGAGGCCGAGGCGGG[C/T]AGATCACCTGAGGTC	4297
rs515934	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118465013	caaagtttgcccttt[G/T]tttgatgagaggaat	4297
rs516511	snp	A/C	0	0	intron-variant	KMT2A	GRCh38.p7	11:118468002	CAAAATAGGTTAAAC[A/C]AATCCTTTTTTTTTT	4297
rs516676	snp	G/T	0	0	upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118525456	CTTAATTCTTGTTAT[G/T]GGTGTAAAAACAGAG	4297
rs517989	snp	A/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118441889	AAGGTGAGCAAAGAG[A/G]TGAGAATTAAGTCAA	4297
rs518835	snp	A/G	3.56347e-05	0.00422091	missense	KMT2A	GRCh38.p7	11:118482090	CCTCCTCACTCACCT[A/G]ATTCTGGTGGTGGAG	4297
rs520124	snp	A/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118496852	catctttaaaatgaa[A/G]ataataacgcttacc	4297
rs521816	snp	A/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118441448	TACACATAGTTCTGA[A/G]AACCTACAGAATCCC	4297
rs524103	snp	C/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118454957	ATATTCGCTAGGGTA[C/G]ACAGGAAAGGCTTCT	4297
rs524616	snp	A/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118498551	CTTTTTTTTTTTTTT[A/T]AAAGCAACTAAAGCT	4297
rs524936	snp	A/G	0.416055	0.186885	intron-variant	KMT2A	GRCh38.p7	11:118471206	ATTGAAGAGCAGCGT[A/G]TTCAAATTTGTTCAA	4297
rs525174	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118446857	CAGATTCTCAGCGCT[C/G]CATGATCTTGCTAGC	4297
rs525177	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118446863	CTCAGCGCTGCATGA[G/T]CTTGCTAGCCTGTAT	4297
rs525549	snp	A/T	0.361684	0.223667	intron-variant	KMT2A	GRCh38.p7	11:118487353	GCATGCTATTCTCTA[A/T]TTTATATTTTAGGAA	4297
rs526168	snp	A/C	0	0	intron-variant	KMT2A	GRCh38.p7	11:118441037	TGAGCTATTTAGTCC[A/C]AACttttcattttac	4297
rs528056	snp	C/T	0.400504	0.199621	intron-variant	KMT2A	GRCh38.p7	11:118447192	TAAAAAATTTAACCC[C/T]GTATACCTTATGTCG	4297
rs529378	snp	C/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118486917	CCTAGCTTGGAtttt[C/T]ttattttttaaattt	4297
rs529862	snp	G/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118471642	ATATATGCTCTTCAT[G/T]GTTTAATTTCTATAC	4297
rs530044	snp	C/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118458272	caacatagtgaaacc[C/T]tctttctataaaaaa	4297
rs530300	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118478935	AACTTCTTAAAAAAA[A/G]AAATTTCATATGAGg	4297
rs531076	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118478906	Ggccaagcactgtgg[C/G]tcatgtttgtaatcc	4297
rs531723	snp	G/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118459036	TGATTCATTGAAATT[G/T]GTTTTGTAATTGAAG	4297
rs532198	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118478743	CATATGCATGAACAT[A/T]TTCTAAGAGAGAGTG	4297
rs532536	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118459109	agagtcttgctctgt[C/T]acccaggctggagtg	4297
rs533942	snp	A/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118478578	GAGCTACAgtctgat[A/T]tggtagccactagtt	4297
rs535327	snp	A/G	0.419135	0.184101	intron-variant	KMT2A	GRCh38.p7	11:118471070	CCACTGAGTTCAGTG[A/G]TCTTATTCTGATGTG	4297
rs536256	snp	C/T	0.489434	0.0719116	intron-variant	KMT2A	GRCh38.p7	11:118456606	TCATGCCTGTAATCC[C/T]AGCACTTTGGGAGGC	4297
rs537975	snp	C/T	0.479744	0.0985793	intron-variant	KMT2A	GRCh38.p7	11:118492154	GAGAAATTTGGACTT[C/T]ATACTCTGAAGGTGA	4297
rs538421	snp	C/T	0.0607341	0.163335	intron-variant	KMT2A	GRCh38.p7	11:118460440	aaatagctgggtgtg[C/T]tggtgcatgcctgtg	4297
rs538739	snp	A/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118461877	ATGTGCTTAAGGAGA[A/G]TGATGGAGCAAGATG	4297
rs542117	snp	A/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118467851	CCTTATTTTGTTCTT[A/G]TTTTATGTGGATTTT	4297
rs542195	snp	C/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118469097	ctgcacccactaact[C/G]gtcatctagcattag	4297
rs542416	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118467426	GAAAAGGCTGAAATT[C/T]TCCTCTTCCAAGACA	4297
rs542534	snp	G/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118498191	TATATCAATACTTGT[G/T]GGCTAACTACCCTGA	4297
rs543370	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118455874	tgtgaaaccccatct[C/G]tacaaagaaaaacac	4297
rs543872	snp	C/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118468048	AATTAGAGGTAAGCA[C/G]AAGCTTTTGCTTTTT	4297
rs543875	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118444229	AAGTTGAATATGGGC[A/G]TGTGTAAATATTTCT	4297
rs545991	snp	A/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118467040	AATTTAAGGAACACA[A/G]ACTACAGTAATTTTT	4297
rs546434	snp	C/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118462516	ACTTTTACCCAAGAA[C/T]TTTCTTTGCACTTGA	4297
rs547745	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118455116	ttcatgtgagcccaa[C/G]agtttgaggctgcag	4297
rs552045	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118451398	aattttcttttctgt[C/T]ctcttttgagacaga	4297
rs552054	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118451405	ttttctgttctcttt[A/T]gagacagagtcttgc	4297
rs552738	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118461891	AGCAACAGGCTTCTC[A/G]TCTTGCTCCATCACT	4297
rs552991	snp	C/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118451509	tctcgtgcctcagcc[C/T]cctgagtagctgaga	4297
rs554423	snp	A/C	0	0	intron-variant	KMT2A	GRCh38.p7	11:118469074	tatacatgtgccatg[A/C]tggtgcgctgcaccc	4297
rs555878	snp	C/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118486334	TAATCCAACCACACT[C/T]TTAATATTTTGGTGT	4297
rs555954	snp	A/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118486307	GTGTGAATCCTTCCA[A/G]ATTGTTTTCTAGATA	4297
rs557465	snp	G/T	0	0	missense	KMT2A	GRCh38.p7	11:118501693	ATTTCAGCTGTGTTT[G/T]GACTCTCTTTGATGA	4297
rs557988	snp	A/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118441705	TTATACTGAGCATTA[A/G]AAATTCAGTCTTTAG	4297
rs558086	snp	A/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118453535	tgtgtagacagagaa[A/G]gcagtgaaaagtaga	4297
rs561775	snp	C/T	0.418814	0.184396	intron-variant	KMT2A	GRCh38.p7	11:118470497	GCAGAGAAACCATGT[C/T]TCATTTCTCAAATAA	4297
rs562780	snp	A/G	0.292953	0.246282	intron-variant	KMT2A	GRCh38.p7	11:118491699	GTCCTCTGAAGAATG[A/G]GAGAGAGGAAGAAGA	4297
rs562795	snp	C/T	0.027022	0.113052	intron-variant	KMT2A	GRCh38.p7	11:118464967	catgatggagcagga[C/T]tctggtgaagctttc	4297
rs562884	snp	C/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118464936	ctgggcatttttcta[C/G]taaagctttggttaa	4297
rs563239	snp	A/G	0	0	splice-acceptor-variant	KMT2A	GRCh38.p7	11:118490128	TTTTCTTCTTTTCTA[A/G]ATCTGTACCAAGTGT	4297
rs563387	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118440729	GAGACAGGCTTTTGG[A/G]TTGGACTTGAAAAGA	4297
rs564518	snp	A/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118509305	CTTCTTTGGAGCTTA[A/G]ATTTTTTTTTTTAAA	4297
rs565741	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118467007	TTTAATTACAtattt[G/T]gctcaggcgggtctt	4297
rs565768	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118466998	Atatttggctcaggc[G/T]ggtctttaattcctg	4297
rs566021	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118459671	ttcaaaaaaaaaaaa[A/T]TTTTTTTCAATATAC	4297
rs566022	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118459668	aaaaaaaaaaaaTTT[A/T]TTTTCAATATACCAT	4297
rs567597	snp	A/C	0	0	intron-variant	KMT2A	GRCh38.p7	11:118466818	aaaacaaaacaaaac[A/C]aaacaaaaacaacaa	4297
rs567777	snp	G/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118451872	CTTTGCAAGATACTT[G/T]GGAAATTGATAATCT	4297
rs570821	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118478667	AAATTATGTTGACCC[A/C]ACCAAATTATGACCA	4297
rs570826	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118478670	TTATGTTGACCCCAC[A/C]AAATTATGACCATTC	4297
rs570920	snp	C/T	0.00338409	0.040995	intron-variant	KMT2A	GRCh38.p7	11:118463111	ACAGTGTGTATCTCT[C/T]ACATTTATCTTTAtt	4297
rs571836	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118463212	atcctcctaccttgt[C/T]ctcccaaaggggtgg	4297
rs572126	snp	C/T	0.430982	0.172469	intron-variant	KMT2A	GRCh38.p7	11:118488446	GTACAGTATTGGACA[C/T]TGCGGGAGATTCAGA	4297
rs572650	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118463263	gcccccagccCATTT[C/T]TTTTAAAGATTAATA	4297
rs573353	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118478889	ggcctcccaaagtac[G/T]gggattacaAACATG	4297
rs573453	snp	G/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118468997	atttatttatttatt[G/T]attattgttatactt	4297
rs573581	snp	C/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118460944	TGTCTTACTCAATGT[C/T]GTATCTGGAACATAT	4297
rs573971	snp	A/G	0.478271	0.101943	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522681	GTGGTTTTCCCTACT[A/G]TCCTCCCACTCGAGA	4297
rs574245	snp	A/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118469051	aatgtgcaagttagt[A/T]acatatgtatacatg	4297
rs574387	snp	A/C	0.492435	0.0610346	intron-variant	KMT2A	GRCh38.p7	11:118466288	tgagccgtgatcaca[A/C]cactgcagtacagcc	4297
rs576818	snp	A/C	0	0	intron-variant	KMT2A	GRCh38.p7	11:118455124	tcaaactcttgggct[A/C]acatgaacctcctgc	4297
rs576950	snp	C/T	0.336702	0.234484	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520660	AAATGAGCGCCCCCC[C/T]TTTTTTTTTGAGATG	4297
rs587197	snp	A/C	0	0	intron-variant	KMT2A	GRCh38.p7	11:118440695	TTCACTTGAAATTGC[A/C]GTTTAGTTCATGTGG	4297
rs591951	snp	C/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118454048	catccaaaataagcc[C/T]taaattcaactacct	4297
rs599397	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118441115	CTTTTGGTCAAATCA[A/G]AATTTCTTATTCTGA	4297
rs607211	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118455114	cactgcagcctcaaa[C/T]tgttgggctaacatg	4297
rs613220	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118441894	TTAATTCTCACCTCT[C/T]TGCTCACATAACAAC	4297
rs616284	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118468063	CAAGCTTTTGCTTTT[G/T]GTCCTTTCCAACTAT	4297
rs624719	snp	C/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118456717	CAGTACTATATTCTT[C/T]CCCTGGGTGACTGAA	4297
rs629470	snp	A/G	0.462253	0.132093	intron-variant	KMT2A	GRCh38.p7	11:118449838	TAACCTGACTTTTGC[A/G]CCAGAATAAGAACAA	4297
rs634436	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118463222	cttgtcctcccaaag[G/T]gctgggattacaggc	4297
rs634464	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118463250	ggcatgagccactgc[A/C]cccagccCATTTCTT	4297
rs635263	snp	C/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118463395	TAGCAATGTAGTCCC[C/T]TAGTAAGTGTTGGGA	4297
rs656347	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118451269	caggctgggatgcag[G/T]ggcacaaacacagct	4297
rs658009	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118451573	tttatgtttttagta[A/G]agacggggtttcacc	4297
rs677075	snp	C/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118439010	TTTGAAAGGCCAATT[C/T]TGTATTTTTTAAGCT	4297
rs688546	snp	A/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118453782	TCTGAAGTATCACTA[A/G]TATTCCCATTTCATA	4297
rs692888	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118446681	TTAAATTTCCATTAC[G/T]TTTGGATAGTTTATT	4297
rs692924	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118447228	CTTTTGAAATGTGTC[G/T]GTCTTTGTCCCATTA	4297
rs693416	snp	A/T	0	0	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520700	ACACTCTTTGTTTAA[A/T]GCCAAACTGAACGAG	4297
rs693598	snp	A/C	0.00383876	0.0436422	missense	KMT2A	GRCh38.p7	11:118498500	AAAAAGTATATTGCC[A/C]ACGACATCGGGATTT	4297
rs693713	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118446768	caatatgatagtttt[C/G]ttaaatacagatcag	4297
rs693715	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118446769	aatatgatagttttc[G/T]taaatacagatcaga	4297
rs762872	snp	C/G	0	0	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118524635	GCCCTAGGGGTTCCA[C/G]TAGTGTCTGCTTTCC	4297
rs1064911	snp	C/G	0	0	missense, intron-variant	KMT2A	GRCh38.p7	11:118472825	AGTGCCCCCCAGCAG[C/G]AGACCTCCTCGTCTC	4297
rs1064920	snp	C/G	0	0	utr-variant-3-prime, intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118524873	GCTGTACTGTGAGCC[C/G]CTCCTCACTCTCTAC	4297
rs1064939	snp	A/T	0.0170251	0.090679	upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118525616	aataaaaaataaaaa[A/T]aaaaggaaaaaaaaa	4297
rs1181236	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118462084	tcagcctcccgagta[C/G]ctgggactacaggcg	4297
rs1181237	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118462138	tttgtatattttgta[A/G]agacggggtttcacc	4297
rs1181238	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118462155	gacggggtttcacca[G/T]gctggccaggctgat	4297
rs1181239	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118462198	gcctcaggtgaccca[A/C]ccatctctaccttcc	4297
rs1181240	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118462208	acccaaccatctcta[A/C]cttccaaagtgctgg	4297
rs1181241	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118462289	TCTTTCCCAGTGCTT[A/T]CTCAACTTGGCTTTA	4297
rs1181249	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118486388	AAAACTCAGAAAGAT[A/T]AAAAAAAAAAAACCA	4297
rs1184724	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118462372	TACATAGGCTTGGAA[A/G]TTCCAAGTTAGAAGA	4297
rs1185373	snp	A/C	0	0	synonymous-codon	KMT2A	GRCh38.p7	11:118498408	GGATGTGAGACAGCA[A/C]CCCACGGTGGCTCCT	4297
rs1185757	snp	A/T	0.495213	0.048687	intron-variant	KMT2A	GRCh38.p7	11:118463137	TTATTTTTTTTTTTT[A/T]AATAAAGATGGGGTC	4297
rs1613361	snp	A/G	0.00557542	0.0525036	intron-variant	KMT2A	GRCh38.p7	11:118457409	GTAGCTGGGACTACA[A/G]GTGCCCACCACCACG	4297
rs1613494	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118457457	ttgtattttttagta[A/G]agacagggtttcacc	4297
rs1619123	snp	A/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118490314	TCTGGAGGTGAACTA[A/G]ACTCTAGTGAAATGA	4297
rs1623291	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118451427	gcactccagcctggg[C/T]gacagggcaagactc	4297
rs1627304	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118441091	ATGATTCCTTTCTGT[G/T]GTATTAAACTTTTGG	4297
rs1734793	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118440826	AGCAACTCCCACTCT[G/T]GGTACATACATGACC	4297
rs1734794	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118441140	CTGGACTCTGACTTT[G/T]GAAATAAACTCAGAA	4297
rs1734795	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118441153	TCAAATCGTCTCACT[G/T]GACTCTGACTTTGGA	4297
rs1784241	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118451444	gccgaaattgcgcca[C/T]tgcactccagcctgg	4297
rs1784242	snp	A/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118451421	cagcctgggcgacag[A/G]gcaagactccatctc	4297
rs1784245	snp	G/T	0	0	missense	KMT2A	GRCh38.p7	11:118480230	ACACTACCTTTAGCT[G/T]GCTTCTGCAGGTAGG	4297
rs1784246	snp	G/T	0	0	missense	KMT2A	GRCh38.p7	11:118480197	TTGGAAGGCATCCAT[G/T]GTAGATTCTGACATT	4297
rs1784247	snp	G/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118480102	AACAAGTGTTCATTT[G/T]GTCTGCAACAATCAG	4297
rs1784253	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118489163	ctggagtggctcact[C/G]caacctctgcctcca	4297
rs1784291	snp	C/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118490262	AAGGTACCCAAAAAA[C/G]CCAGTTTTGCCAGCT	4297
rs1786442	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118441187	tttttgttttttttt[G/T]gagtcagggtctcac	4297
rs1786445	snp	A/C	0	0	intron-variant	KMT2A	GRCh38.p7	11:118454866	CATCAATTGTTCTGC[A/C]AGttaaaattaaaaa	4297
rs1786446	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118452726	caatcgcttgaaccc[A/C]ggaggcggaggttgc	4297
rs1786450	snp	G/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118486829	gtgataatggctcac[G/T]gcagcctcgatctcc	4297
rs1786451	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118486820	gctcactgcagcctc[A/G]atctcctgggctcaa	4297
rs1786475	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118453448	ttcttcttaactcat[G/T]ggctgttaattttca	4297
rs1786478	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118486753	tagcatgtgcctgta[G/T]tcccagctactctag	4297
rs1786479	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118486787	cagctatttgggagg[C/G]tgaggtgagaggatc	4297
rs1786482	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118449500	ccattgggctcaagc[A/C]atcctcccatcacag	4297
rs1786483	snp	G/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118480266	TAAGCAAGGAGCATT[G/T]GGGGGAAGACCTTTT	4297
rs1786484	snp	G/T			missense	KMT2A	GRCh38.p7	11:118480211	TCTGCAGGTAGGCTT[G/T]GGAAGGCATCCATGG	4297
rs1803763	snp	C/T			synonymous-codon	KMT2A	GRCh38.p7	11:118505495	TCCCCAACTTTTGGT[C/T]TCAGAATCCAGCCAG	4297
rs1939950	snp	A/G	0.105214	0.203807	intron-variant	KMT2A	GRCh38.p7	11:118441401	TTTTCTTATAAATGA[A/G]ACTGGTCAACTTCCC	4297
rs2017122	snp	C/T	0.0693013	0.172766	intron-variant	KMT2A	GRCh38.p7	11:118444134	AGTTTTTTCTTTAGG[C/T]TGTCCTTTATACTAT	4297
rs2071702	snp	C/T	0.11063	0.207547	KMT2A	11	allele_origin=T(germline)/C(germline)	11:118503146	ATCATCCATTATCAA[C/T]GAACATATGGGATCT	4297
rs2276045	snp	C/T	0.0667028	0.170006	intron-variant	KMT2A	GRCh38.p7	11:118494453	AGTTCATTGTATTCA[C/T]AGGGTAATTACTTAT	4297
rs2276058	snp	A/G	0.00191674	0.0308982	synonymous-codon, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520026	CTCCTCTTCTTCATC[A/G]TTGGGGTTGTATTCA	4297
rs2471830	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118441927	TCCTTCCGTGGGGCA[A/G]CTGTGCAAACTCTAT	4297
rs2471831	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118441935	TGGGGCAACTGTGCA[A/G]ACTCTATACCAAAGG	4297
rs2509829	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118439183	aaaaaagaaaaaaaa[A/G]aaaaaaaGGGAATTT	4297
rs2509830	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118440831	GGTTTGTACCAAGAG[G/T]GGGAGTGGCTCCTTC	4297
rs2734668	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118441971	CTTACCCTGTGGCTA[A/G]AGGGGGTGGCAACAG	4297
rs2734670	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118437153	GGCCCATCTGGCTGA[A/G]GGCGTTTGCCCCCCG	4297
rs3016464	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118451636	tcaggtgatccaccc[A/C]cctcggcctcccaaa	4297
rs3016465	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118451639	ggtgatccacccacc[C/T]cggcctcccaaagtg	4297
rs3016948	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118486405	TCTTTCTGAGTTTTT[G/T]GCAGTATGTACCACC	4297
rs3016949	snp	G/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118486473	TAGGAAGCAGTAGTT[G/T]GTCATTTATAAGGGA	4297
rs3016950	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118486522	CAGTTCTTAAATTCC[G/T]GGCAGATACCTCTTG	4297
rs3115538	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118457288	tttttttttttttga[A/G]acaaaatcttgctct	4297
rs3115539	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118457294	tttttttgaaacaaa[A/G]tcttgctctgtcacc	4297
rs3115541	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118436967	GGCGAGGAACCCCCA[A/G]GTCCGGGGTCTCGAC	4297
rs3115542	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118436994	CGACCCTCTGCGGAG[A/C]CCCCTCCCCTCCCCC	4297
rs3132786	snp	A/G	0.482083	0.0929373	intron-variant	KMT2A	GRCh38.p7	11:118495241	AACCAGGGAGGCGGA[A/G]GTTGTAGTGAGCCGA	4297
rs3132888	snp	C/G			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522628	ACGCTGTAGGTGGGG[C/G]CTGGCTGGCAAACTG	4297
rs3132889	snp	C/G	0	0	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522577	CCATTTGGGGCTTTG[C/G]CTGACCCACTCACTT	4297
rs3132890	snp	C/G			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522630	GTTTGCCAGCCAGGC[C/G]CCACCTACAGCGTCT	4297
rs3132894	snp	A/C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118452633	CCTTCtttttttttt[A/C/T]ctttcttgttttttt	4297
rs3205893	snp	A/G	0	0	synonymous-codon	KMT2A	GRCh38.p7	11:118504013	CCATAATTTATTTCG[A/G]GAGGAGGAACAGTGT	4297
rs4018726	snp	A/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118470772	AAAGAAGATTTGAGT[A/G]AAGATAGCCTAGTCT	4297
rs4121657	snp	C/T			missense	KMT2A	GRCh38.p7	11:118490165	TGTAAGAGCTGTGGA[C/T]CCACAACCCCAAGCA	4297
rs4121658	snp	C/T			synonymous-codon	KMT2A	GRCh38.p7	11:118490173	CTGTGGACCCACAAC[C/T]CCAAGCAAAGGGTGG	4297
rs4628712	snp	A/C/G/T	0	0	splice-acceptor-variant	KMT2A	GRCh38.p7	11:118497934	ATCTCTTTATTTTAT[A/C/G/T]GGATGCTGGTCGTTT	4297
rs4938511	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118507192	agccccagctattca[A/G]gaggctgaggtggga	4297
rs4938512	snp	G/T	0.00755907	0.0610114	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118517147	acgcctgtaatccca[G/T]cactttgggaggctg	4297
rs7103001	snp	A/T	0.0667028	0.170006	intron-variant	KMT2A	GRCh38.p7	11:118496954	agcTACAATTTTTTT[A/T]AAAGTTttttgtgtt	4297
rs7107035	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118497677	tgctgggattacaga[C/T]gtgaaccaccatacc	4297
rs7107305	snp	A/G	0.0937416	0.195149	KMT2A	11	allele_origin=G(germline)/A(germline)	11:118497950	GGATGCTGGTCGTTT[A/G]CTATATATTGGCCAA	4297
rs7110169	snp	A/G	0.0482946	0.147699	intron-variant	KMT2A	GRCh38.p7	11:118445763	atcccagcactttgg[A/G]aggccaaggcgggaa	4297
rs7111656	snp	C/T	0.0329836	0.124112	intron-variant	KMT2A	GRCh38.p7	11:118462022	agtggcgtgagcttt[C/T]ggctcaatgcaacct	4297
rs7113959	snp	A/T	0.130351	0.219509	intron-variant	KMT2A	GRCh38.p7	11:118508381	TGtggATCTACAATA[A/T]TTTAATGAGTCCTCT	4297
rs7113994	snp	A/G	0.136506	0.222754	intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118511612	TTTGATTAGGGGTAC[A/G]GGGAACATAAAAATA	4297
rs7116876	snp	C/G	0.0670745	0.170406	intron-variant	KMT2A	GRCh38.p7	11:118500310	AATCCACACAATAAT[C/G]ATCAAATTTTTCAAT	4297
rs7123835	snp	G/T	0.0938124	0.195206	intron-variant	KMT2A	GRCh38.p7	11:118498107	ATTTTATGAAAGAGA[G/T]TCCCTCTCAGTTTCC	4297
rs7125489	snp	A/G	0.0325976	0.123435	intron-variant	KMT2A	GRCh38.p7	11:118461802	TCTTTTGATTTCTAG[A/G]TAAGTTTAAATCCTT	4297
rs7128022	snp	A/G	0.0379877	0.132479	intron-variant	KMT2A	GRCh38.p7	11:118474698	TTAAACCAGGGACTT[A/G]ATTGTAAAGGTACAT	4297
rs7350516	snp	G/T	0	0	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118513170	gatcactggagccta[G/T]gagtatgagactgta	4297
rs7479333	snp	A/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118492282	agacacctgagccta[A/G]aggcaggattcgtag	4297
rs7931377	snp	A/G	0.00318978	0.0398085	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118515783	aacctccgcctcccg[A/G]gttcaagcaatactc	4297
rs7932119	snp	C/T	0.00279162	0.0372561	intron-variant	KMT2A	GRCh38.p7	11:118486407	tttctgagttttttg[C/T]agtatgtaccacctt	4297
rs7933684	snp	A/G	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118470845	CAGTCTTGTTTTCTT[A/G]AATGGCTTGAAAAGC	4297
rs7937140	snp	C/T	0.0566069	0.158427	intron-variant	KMT2A	GRCh38.p7	11:118477586	gatctcggctcacta[C/T]agcctccacttccca	4297
rs7939770	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118488302	CTCCCTATTTCCCCC[A/C]CCCCACTCCTTTATA	4297
rs7941217	snp	C/T	0.202959	0.245534	intron-variant	KMT2A	GRCh38.p7	11:118478532	gactgaggaaccaca[C/T]tgtttatttcgttta	4297
rs7947299	snp	A/T	0.0023933	0.0345097	intron-variant	KMT2A	GRCh38.p7	11:118486514	ATCCTTTACAGTTCT[A/T]AAATTCCTGGCAGAT	4297
rs7948661	snp	C/T	0.108048	0.20579	intron-variant	KMT2A	GRCh38.p7	11:118470934	TTTAATAAGTTGTCA[C/T]TTTGCTGTTGACATC	4297
rs7951019	snp	G/T	0.0225045	0.103662	intron-variant	KMT2A	GRCh38.p7	11:118487312	GATCTAAATTCTTTA[G/T]AGTTGTACATAGCAA	4297
rs9332742	snp	C/T	0.000842105	0.0205023	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118434793	CCCCATCCTGCGCGG[C/T]TGGAACGAAGATCGA	4297
rs9332743	snp	C/G	0.00318978	0.0398085	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118435205	CCAACGCAAGTTCTC[C/G]CGACACAAACCCCTC	4297
rs9332744	snp	C/T	0.0185938	0.0946107	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118436165	GCGCTCTGCTCCGGG[C/T]TCCCGGGCTTCCTTC	4297
rs9332745	snp	C/G	0.0246875	0.108325	KMT2A	11	allele_origin=G(germline)/C(germline)	11:118436601	ggggcctagggggcg[C/G]cccgcggcaacgcgt	4297
rs9332746	snp	A/G	0.0116955	0.0755709	synonymous-codon	KMT2A	GRCh38.p7	11:118436647	tccccccgggccccc[A/G]gtcggcggtggcggc	4297
rs9332747	snp	C/T	0.0183471	0.0940048	missense	KMT2A	GRCh38.p7	11:118436670	gtggcggccccgggg[C/T]gccccccTCCCCCCc	4297
rs9332749	snp	G/T	0.00199481	0.0315187	intron-variant	KMT2A	GRCh38.p7	11:118437442	GGGGATCGTGTCCCT[G/T]CCAGCACCTTGCTTT	4297
rs9332750	snp	A/C	0.0232847	0.105357	intron-variant	KMT2A	GRCh38.p7	11:118437682	CAGTCTCTTCCCCCC[A/C]CCGCCCCGTCTTACA	4297
rs9332751	snp	C/G/T	0.00517822	0.0506191	intron-variant	KMT2A	GRCh38.p7	11:118437683	AGTCTCTTCCCCCCC[C/G/T]CGCCCCGTCTTACAG	4297
rs9332752	snp	G/T	0.00914312	0.0669923	intron-variant	KMT2A	GRCh38.p7	11:118446991	TCTGCCTTTGTACCT[G/T]TGCTAAAGCCTCTCC	4297
rs9332753	snp	A/G	0.00478085	0.0486577	intron-variant	KMT2A	GRCh38.p7	11:118447082	TCAACTCAGATCCCC[A/G]GATCCTAACTCTTCC	4297
rs9332754	snp	A/G	0.046775	0.145601	intron-variant	KMT2A	GRCh38.p7	11:118447223	TGGTACTTTTGAAAT[A/G]TGTCTGTCTTTGTCC	4297
rs9332755	snp	G/T	0.0554779	0.157039	intron-variant	KMT2A	GRCh38.p7	11:118447464	ACTAATTTAAGTATG[G/T]CAAAGGAAAGCACAG	4297
rs9332756	snp	A/G	0.0329836	0.124112	intron-variant	KMT2A	GRCh38.p7	11:118457866	CCTCTAGCATAGCAG[A/G]CAACATACGATACTT	4297
rs9332757	snp	A/G	0.00636936	0.0560724	intron-variant	KMT2A	GRCh38.p7	11:118458528	TATTTTCATTTTACA[A/G]ACATTTATTGGGTGC	4297
rs9332758	snp	A/C	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118458878	TTAGTTGTTCTCAGT[A/C]ATTTTGTTAGTTCTC	4297
rs9332759	snp	G/T	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118459029	TTTCAATTGATTCAT[G/T]GAAATTTGTTTTGTA	4297
rs9332760	snp	C/T	0.0110494	0.0735024	intron-variant	KMT2A	GRCh38.p7	11:118467741	ATACATGTGTTCTTA[C/T]CTCTCGAGAGGAAAA	4297
rs9332761	snp	C/T	0.00716266	0.059414	intron-variant	KMT2A	GRCh38.p7	11:118468025	TTTTTTTTTATAGAG[C/T]AGGTTAAAATTAGAG	4297
rs9332762	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118468576	TACTACACAGCTCCT[A/G]TTTGTCTGTAATAAA	4297
rs9332763	snp	C/T	0.00335007	0.0407899	intron-variant	KMT2A	GRCh38.p7	11:118468943	GGATGCTCTACCATA[C/T]TTGGGTTAGGAAATG	4297
rs9332764	snp	A/C	0.0240643	0.107019	intron-variant	KMT2A	GRCh38.p7	11:118469140	atgctatccctcccc[A/C]ctccccccaGCTAGA	4297
rs9332765	in-del	-/AT	0.0118339	0.076006	intron-variant	KMT2A	GRCh38.p7	11:118469336	TGTGGTAGTGTATAT[-/AT]GTCTTTGGGAATAAT	4297
rs9332766	snp	C/G	0.0146672	0.084371	intron-variant	KMT2A	GRCh38.p7	11:118469778	TAGCTTGTGATGTGT[C/G]CTAGCATTAGGGTCT	4297
rs9332767	snp	C/T	0.0111728	0.0739025	intron-variant	KMT2A	GRCh38.p7	11:118470501	TTGAGAAATGAAACA[C/T]GGTTTCTCTGCTGTC	4297
rs9332768	snp	G/T	0.00199481	0.0315187	intron-variant	KMT2A	GRCh38.p7	11:118470778	AGATTTGATAAAATA[G/T]CCTAGTCTTACTACT	4297
rs9332769	snp	A/G	0.0170251	0.090679	intron-variant	KMT2A	GRCh38.p7	11:118470805	TACTTTTTAAAATAC[A/G]GGTTTATACAAGGTG	4297
rs9332770	snp	A/G	0.0146672	0.084371	intron-variant	KMT2A	GRCh38.p7	11:118470807	CTTTTTAAAATACAG[A/G]TTTATACAAGGTGTT	4297
rs9332771	snp	C/T	0.0569829	0.158885	intron-variant	KMT2A	GRCh38.p7	11:118471117	TTCTATTCAGTAAAA[C/T]TTTCTTAGTCTACTT	4297
rs9332772	snp	A/C/G	0.0124131	0.0777976	missense, intron-variant	KMT2A	GRCh38.p7	11:118472663	CAGGTACTTCCTGAG[A/C/G]AGCGGAGCGATACCC	4297
rs9332773	snp	C/T	0.00553948	0.052336	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473133	CCCTCCACTAACTCC[C/T]GAGGACGTTGGCTTT	4297
rs9332774	snp	C/T	3.29462e-05	0.00405857	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118474132	GAAAACCCTCTGCCT[C/T]TCCACTCCTTCATCT	4297
rs9332775	snp	A/T	0.0448719	0.142907	intron-variant	KMT2A	GRCh38.p7	11:118474402	AGTGGTTCAATTACA[A/T]CCAGTTATGAGAACC	4297
rs9332776	snp	G/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118474571	ATTTGAGGAATACTG[G/T]ATAGCTGGATTGGCA	4297
rs9332777	snp	A/G	0.0115603	0.0751433	intron-variant	KMT2A	GRCh38.p7	11:118475059	aatctcttgaacccc[A/G]gaggtagagatggca	4297
rs9332778	snp	A/G/T	0.00159649	0.0282165	intron-variant	KMT2A	GRCh38.p7	11:118475680	gtgagccgagatcac[A/G/T]gcactacactccagc	4297
rs9332779	snp	A/G	0.0119091	0.0762411	intron-variant	KMT2A	GRCh38.p7	11:118475710	cctgggtgacagggc[A/G]agactccgtctctaa	4297
rs9332780	snp	G/T	0.00557542	0.0525036	intron-variant	KMT2A	GRCh38.p7	11:118475852	ATGTTGGATGTTTTT[G/T]TGATAGGAGCAGCGG	4297
rs9332781	snp	A/G	0.0696718	0.173152	intron-variant	KMT2A	GRCh38.p7	11:118475884	TCTTTAAAATCTGAG[A/G]CATTTCTTTTGGAGC	4297
rs9332782	snp	C/T	0.0146672	0.084371	intron-variant	KMT2A	GRCh38.p7	11:118476305	ACCACACTGAACTTT[C/T]TGATAATATAGACTG	4297
rs9332783	snp	A/G	0.00833332	0.0640095	synonymous-codon	KMT2A	GRCh38.p7	11:118476939	CCTGAGTGCCTTACC[A/G]TGGGAAGAACGAGAA	4297
rs9332784	snp	A/G	0.00953873	0.0683987	intron-variant	KMT2A	GRCh38.p7	11:118477669	TGTGCCACCATGCCT[A/G]GCTAATTTTTGTATT	4297
rs9332785	snp	G/T	0.0150606	0.0854603	intron-variant	KMT2A	GRCh38.p7	11:118477699	ttttagtagagaggg[G/T]ttttgctatgttggc	4297
rs9332786	snp	G/T	0.0148549	0.0848926	intron-variant	KMT2A	GRCh38.p7	11:118478248	CTCTCAACCATAAAG[G/T]TTGCTTATTTATCCC	4297
rs9332787	snp	A/G	0.0125781	0.0782997	intron-variant	KMT2A	GRCh38.p7	11:118478410	gaatgttctgcaaca[A/G]tggaaatgttctatt	4297
rs9332788	snp	A/C	0.00716266	0.059414	intron-variant	KMT2A	GRCh38.p7	11:118478973	aatttttatgggtac[A/C]tagtaggtatatata	4297
rs9332789	snp	A/G	0.0115603	0.0751433	intron-variant	KMT2A	GRCh38.p7	11:118479256	AATTTTTTATGTGGA[A/G]ATTTTTATTACTCTA	4297
rs9332790	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118479656	AAGTTGCATTAAATT[C/T]AAGAGTTAAAGTGGA	4297
rs9332791	snp	A/C	0.0147029	0.0844706	intron-variant	KMT2A	GRCh38.p7	11:118480265	AAAAAGGTCTTCCCC[A/C]AAATGCTCCTTGCTT	4297
rs9332792	snp	A/G	0.0158469	0.0875917	intron-variant	KMT2A	GRCh38.p7	11:118480386	ggtaataggtacatg[A/G]gggttgattggacta	4297
rs9332793	snp	A/G	0.0696718	0.173152	intron-variant	KMT2A	GRCh38.p7	11:118483743	ATTTTTATTTATTAT[A/G]GATAAAGAGATAgtg	4297
rs9332794	snp	G/T	0.0696718	0.173152	intron-variant	KMT2A	GRCh38.p7	11:118483790	taatcccagcacttt[G/T]gggggccaaggcggg	4297
rs9332795	snp	C/G	0.0115144	0.0749975	intron-variant	KMT2A	GRCh38.p7	11:118483791	aatcccagcactttg[C/G]ggggccaaggcggga	4297
rs9332796	snp	A/T	0.097727	0.198275	intron-variant	KMT2A	GRCh38.p7	11:118484035	agacccagtctcttt[A/T]aaaaaaaaaTTCAAA	4297
rs9332797	snp	A/G	0.00279162	0.0372561	intron-variant	KMT2A	GRCh38.p7	11:118484124	GCATTATTATCTGTT[A/G]CAAATGTGAAGGCAA	4297
rs9332798	snp	A/G	0.0044033	0.0467147	intron-variant	KMT2A	GRCh38.p7	11:118484334	AGGTGTTCAGTGATC[A/G]TAAAGTATATTGAGT	4297
rs9332799	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118484521	TGCAGAACATACATA[A/G]TGAAACATTCCTATC	4297
rs9332800	snp	A/G	0.0118339	0.076006	intron-variant	KMT2A	GRCh38.p7	11:118484697	GCCTTTTAATAGTCC[A/G]TGTCTGAGATTAAAA	4297
rs9332801	snp	A/C	0.0949095	0.196079	KMT2A	11	allele_origin=A(germline)/C(germline)	11:118484927	GACTTCTGTTCCTAT[A/C]ACACCCAGGGTGGTT	4297
rs9332802	snp	A/G	0.00438332	0.0466095	intron-variant	KMT2A	GRCh38.p7	11:118487695	atcaaggacgttctc[A/G]tatttaaccatggta	4297
rs9332803	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118487738	caggaaattaacaca[C/T]tggtacattactatt	4297
rs9332804	snp	A/C	0.00339558	0.0410641	intron-variant	KMT2A	GRCh38.p7	11:118488219	ACAATTAAAAAAATA[A/C]AATTACAAATGGAAA	4297
rs9332805	in-del	-/T	0.0170251	0.090679	intron-variant	KMT2A	GRCh38.p7	11:118489298	aatgctgcaccattt[-/T]gtctagggacttggg	4297
rs9332806	snp	C/T	1.67428e-05	0.00289329	intron-variant	KMT2A	GRCh38.p7	11:118489915	CATGATGCTCTTTTA[C/T]AGAGAACCACCATGT	4297
rs9332807	snp	A/G	0.0123036	0.0774623	intron-variant	KMT2A	GRCh38.p7	11:118490430	CTTGTTAGTTTATAC[A/G]GGAAGTGTTAAGGGG	4297
rs9332808	snp	A/G	0.0123036	0.0774623	intron-variant	KMT2A	GRCh38.p7	11:118490756	ATGAAGGTTATACAG[A/G]GTACTGAATCTTAGG	4297
rs9332809	snp	A/G	0.0667028	0.170006	intron-variant	KMT2A	GRCh38.p7	11:118490757	TGAAGGTTATACAGA[A/G]TACTGAATCTTAGGA	4297
rs9332810	snp	A/G	0.0573587	0.15934	intron-variant	KMT2A	GRCh38.p7	11:118491019	TCTGTGAGTATTCGA[A/G]GGGCTCAGAATAATC	4297
rs9332811	snp	C/T	0.0119091	0.0762411	intron-variant	KMT2A	GRCh38.p7	11:118491139	ATGCAAGTCGAGGGC[C/T]GTAAAAACACGGGTA	4297
rs9332812	in-del	-/T	0.0118339	0.076006	intron-variant	KMT2A	GRCh38.p7	11:118491995	CTAGTGTTTTTCTTT[-/T]GTTTTACTTCATTCT	4297
rs9332813	snp	A/G	0.0162398	0.0886349	intron-variant	KMT2A	GRCh38.p7	11:118492492	agaccatcctggcta[A/G]cacggtgaaaccccg	4297
rs9332814	snp	A/G	0.00874735	0.0655527	intron-variant	KMT2A	GRCh38.p7	11:118492611	gtgaacctgggcggc[A/G]gagcttgcagtaagc	4297
rs9332815	snp	C/T	0.0115144	0.0749975	intron-variant	KMT2A	GRCh38.p7	11:118492854	AATTATCAAGAAAAG[C/T]TCCTAAGTTACCCTA	4297
rs9332816	snp	G/T	0.199873	0.244923	intron-variant	KMT2A	GRCh38.p7	11:118493689	ATGATCTATATTTGC[G/T]ATTCTGTTGTTTATT	4297
rs9332817	snp	C/G	0.0225045	0.103662	intron-variant	KMT2A	GRCh38.p7	11:118494495	ACTTTTTGCTTTGTG[C/G]TGTGTATAAAACATC	4297
rs9332818	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118494497	TTTTTGCTTTGTGGT[A/G]TGTATAAAACATCTT	4297
rs9332819	snp	C/T	0.150333	0.229274	intron-variant	KMT2A	GRCh38.p7	11:118494548	ATTCTTTGAGAGGAA[C/T]TTGGTGAGGTTGCCA	4297
rs9332820	snp	A/G	0.0142736	0.0832652	intron-variant	KMT2A	GRCh38.p7	11:118495355	tagagactgggtttc[A/G]ccattttggccagga	4297
rs9332821	snp	C/T	0.0023933	0.0345097	intron-variant	KMT2A	GRCh38.p7	11:118495357	gagactgggtttcac[C/T]attttggccaggatg	4297
rs9332822	snp	C/T	0.0298908	0.118541	intron-variant	KMT2A	GRCh38.p7	11:118495409	gatccgcctgcctca[C/T]cctcccaaaagtgct	4297
rs9332823	snp	C/T	0.0166325	0.0896639	intron-variant	KMT2A	GRCh38.p7	11:118495604	TCTGTGAATGGCTCC[C/T]ACATGGGGCAACAGG	4297
rs9332824	snp	C/T	0.00636936	0.0560724	intron-variant	KMT2A	GRCh38.p7	11:118496013	GAATTTTCAGGTCAT[C/T]CTTAAATGTAATACC	4297
rs9332825	snp	C/T	0.0023933	0.0345097	intron-variant	KMT2A	GRCh38.p7	11:118497471	catgcttttggctca[C/T]tgcaatctcggcttc	4297
rs9332826	snp	C/G	0.021333	0.101051	intron-variant	KMT2A	GRCh38.p7	11:118497623	ggctggtctcaaact[C/G]ttgggctcaagcgat	4297
rs9332827	snp	A/G	0.00279162	0.0372561	intron-variant	KMT2A	GRCh38.p7	11:118497783	TGGAAACAGAGCAAC[A/G]TTGCAAAAAGAATTC	4297
rs9332828	snp	G/T	0.00349039	0.0416295	intron-variant	KMT2A	GRCh38.p7	11:118498140	ATATTCTTCCTGTGG[G/T]TGAATATGGCCTCCC	4297
rs9332829	snp	C/G	0.00358779	0.0422022	intron-variant	KMT2A	GRCh38.p7	11:118499159	GGCACCACCTCTTTT[C/G]GGAAATACAGAAGTG	4297
rs9332830	in-del	-/GCTGTATATATCATTGGGGAAATTTCTGGTCCTCAGTTATAAAATGACCCTCAGCCAGGTGTGGTGTCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGCAGATCACTGGAGGTTCAGGAG	0.0558198	0.157461	intron-variant	KMT2A	GRCh38.p7	11:118499579	ctggaggttcaggag[lengthTooLong]ttggagaacagcctg	4297
rs9332831	snp	A/G	0.00358779	0.0422022	intron-variant	KMT2A	GRCh38.p7	11:118500324	TGATCAAATTTTTCA[A/G]TAAGAATTTATAATC	4297
rs9332832	snp	C/T	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118500358	CCTATATGAAGTAAG[C/T]TGTTAAAATGTCTAA	4297
rs9332833	snp	A/T	0.00350262	0.0417018	intron-variant	KMT2A	GRCh38.p7	11:118500868	AGAACCCATAAAATA[A/T]AGCTAAACTCTGTAA	4297
rs9332834	snp	C/T	0.00269085	0.0365812	synonymous-codon	KMT2A	GRCh38.p7	11:118501071	GTGCCGTCCTCCAGT[C/T]GTAGAGCCGGATATC	4297
rs9332835	snp	A/G	0.0667028	0.170006	intron-variant	KMT2A	GRCh38.p7	11:118502208	cagtaagccgagatc[A/G]caccactgcactcca	4297
rs9332836	snp	G/T	0.0185938	0.0946107	intron-variant	KMT2A	GRCh38.p7	11:118502259	cactgtctcaaaaaa[G/T]taataataaataaat	4297
rs9332837	snp	A/T	0.00932748	0.0676516	missense	KMT2A	GRCh38.p7	11:118502856	AAGAGCTCAGAGGGA[A/T]CTGCACATAATGTGG	4297
rs9332838	snp	C/G/T	0.00108682	0.0232861	missense	KMT2A	GRCh38.p7	11:118502962	GCTCCTTTGCTGAAC[C/G/T]CTCTTCAGTGTCGTT	4297
rs9332839	snp	A/G	0.00333889	0.0407222	missense	KMT2A	GRCh38.p7	11:118503061	ACACAGATTCTACCC[A/G]ATCAGCAAACTCCTC	4297
rs9332840	snp	A/G	0.00478329	0.0486699	synonymous-codon	KMT2A	GRCh38.p7	11:118503581	CACAGAACCAATTTC[A/G]GCCTCTGAAAATCCA	4297
rs9332841	snp	C/T	0.00301246	0.0386931	synonymous-codon	KMT2A	GRCh38.p7	11:118504542	AATCTTGGTGAAGGA[C/T]TGGGTCTTGACAGTA	4297
rs9332842	snp	A/T	0.0106051	0.0720423	KMT2A	11	allele_origin=T(germline)/A(germline)	11:118504853	AGGAGTAGATCCAAC[A/T]CCTGAAGGCCACATG	4297
rs9332843	snp	A/G	0.00503684	0.0499304	synonymous-codon	KMT2A	GRCh38.p7	11:118506101	GCCTGTGGCTTTACC[A/G]CCAAGTTCAGGAATG	4297
rs9332844	snp	A/T	0.00147402	0.0271079	synonymous-codon	KMT2A	GRCh38.p7	11:118506638	GACATCCCTGACCTC[A/T]GGCACAGGGTGAGAG	4297
rs9332845	snp	A/G	0.0121208	0.0768991	intron-variant	KMT2A	GRCh38.p7	11:118506746	GACACTCTTCTGTTC[A/G]AGTTGCATTACCTGG	4297
rs9332846	snp	A/G	0.0744748	0.178019	intron-variant	KMT2A	GRCh38.p7	11:118506808	TGAGTGGTGATTTAT[A/G]TAACAAAATGTAGTT	4297
rs9332847	snp	C/T	0.0023933	0.0345097	intron-variant	KMT2A	GRCh38.p7	11:118506972	GGGCAAAGCTCCCTC[C/T]TGTAGATCCACAGAG	4297
rs9332848	snp	C/T	0.00523274	0.0508821	intron-variant	KMT2A	GRCh38.p7	11:118507479	CCTCCACATTCAGTA[C/T]ATATTTACTGGTGGT	4297
rs9332849	snp	A/G	0.0295035	0.117819	intron-variant	KMT2A	GRCh38.p7	11:118507789	acatggtgaaacccc[A/G]tctctactaaaaata	4297
rs9332850	snp	A/G	0.0498117	0.149749	intron-variant	KMT2A	GRCh38.p7	11:118508357	AAATCGCTGCCGCCA[A/G]TTCTATTGTGTGGAT	4297
rs9332851	snp	C/T	0.0379877	0.132479	intron-variant	KMT2A	GRCh38.p7	11:118510303	AATAGCCATATTTTA[C/T]ATGAAAAGTTAATGA	4297
rs9332852	snp	C/T	0.0681886	0.171594	intron-variant	KMT2A	GRCh38.p7	11:118510354	TTGCACACACCTTAG[C/T]GGAGCCCCTGAGAAC	4297
rs9332853	snp	A/G	0.0162398	0.0886349	intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118511666	AGACTTCCATCAAGG[A/G]ATGTGAATGCGTTGG	4297
rs9332854	snp	C/T	0.00675668	0.0577294	intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118511854	GGCAAGTGTTCACAC[C/T]GTAGGGATTCTAAGC	4297
rs9332855	snp	A/G	0.0271762	0.113356	intron-variant, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512089	AATTGTTCGCCTAAG[A/G]CAGAGTTGATTCTGT	4297
rs9332856	snp	A/G	0.00119737	0.0244387	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118518380	atGCTCATTAACAGC[A/G]TGAGACGGTGAGTAG	4297
rs9332857	snp	C/T	0.0681886	0.171594	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118518725	gaggtggagttgtag[C/T]gagctgagatcggac	4297
rs9332858	snp	A/C	0.198944	0.244731	intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118519367	CATTTCTGTGTAATA[A/C]AGCAAAATAGTCCat	4297
rs9332859	snp	A/G	1.64963e-05	0.00287192	missense, nc-transcript-variant, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519620	CTGATTCTTCTAGGT[A/G]TTAACGGTTTGAGGA	4297
rs9332860	snp	A/G	0.00140553	0.0264724	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519909	CCATCATCCTTTACT[A/G]CTTTATTAAAGCATT	4297
rs9332862	snp	A/G	0.00369176	0.0428048	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520083	AGTCTTGAGTGGGGA[A/G]CAGTCATTAGAAACT	4297
rs9332863	snp	C/T	0.0463947	0.145069	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520965	CAAATGCTGGAGTGA[C/T]CTTCCTCACTCAGTA	4297
rs9332864	snp	A/G	0.0221141	0.102801	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521493	GACCCCTGGATCACA[A/G]AAGAAATAGTGTATG	4297
rs9332865	snp	A/G	0.0431296	0.140373	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521851	TGTTCTTAAAGCTGA[A/G]TTTATAAGAAATGAC	4297
rs9332866	snp	C/G/T	0.013097	0.0799021	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522327	GTCCTATACTCACAT[C/G/T]AGACATGTGATCATA	4297
rs9332867	snp	A/G	0.0718919	0.175435	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522469	GCCTGGAAGGAGCCT[A/G]TTATAGAGGGTTGGT	4297
rs9332868	snp	A/G	0.0138799	0.0821421	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522708	GAGAGTTCACTTCTG[A/G]TTGGGAGACAGGATT	4297
rs9332869	snp	C/T	0.0174175	0.0916809	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522841	TATCTCAGCCAATTA[C/T]CTTTCTTGACAGTAG	4297
rs9332870	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522941	TTCCCATGCTTCTTT[C/T]GGGTTGTAGGGGAGA	4297
rs9332871	snp	G/T	0.0763149	0.179815	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118523141	ATGTAGCATGATTTT[G/T]TAGGAGAGGAAAAAG	4297
rs9332872	snp	A/G	0.0130921	0.0798413	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118523399	GTGCAACCCACAGCT[A/G]AAGTAAATTCAATGA	4297
rs10219358	snp	A/G	0.00279162	0.0372561	intron-variant	KMT2A	GRCh38.p7	11:118496861	aatgaagataataac[A/G]cttacctcagagtgg	4297
rs11216871	snp	C/T	0.0023933	0.0345097	intron-variant	KMT2A	GRCh38.p7	11:118450852	TGACTGGTTGAATTT[C/T]ATTAACTATTTGGCT	4297
rs11216872	snp	A/G	0.0170251	0.090679	intron-variant	KMT2A	GRCh38.p7	11:118453904	accttttccattccc[A/G]gtctctttgtttctt	4297
rs11216874	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118475607	atgcgcctgtagtcc[C/T]agctactcgggaggc	4297
rs11216875	snp	A/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118482767	CAAAAAAAAAAAAAA[A/G]AAGAAGAAGAAGAAG	4297
rs11216876	snp	C/T	0.0023933	0.0345097	intron-variant	KMT2A	GRCh38.p7	11:118485089	ATTCCCTGTTTAAAC[C/T]AGCTAAAGAAATGTT	4297
rs11216878	snp	A/G	0.00318978	0.0398085	intron-variant	KMT2A	GRCh38.p7	11:118492608	ggcgtgaacctgggc[A/G]gcggagcttgcagta	4297
rs11216879	snp	C/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118501511	AACTTGAATTCGATT[C/T]AGGGAGTACTATGAT	4297
rs11299231	in-del	-/A	0	0	intron-variant	KMT2A	GRCh38.p7	11:118483377	CTCTACTAAAAATAC[-/A]AAAAAATTAGCCCGG	4297
rs11374365	in-del	-/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118515682	TTTCTTTTTCTGTCC[-/T]TTTTTTTTTTTTTTT	4297
rs11412289	in-del	-/A	0	0	intron-variant	KMT2A	GRCh38.p7	11:118489231	AAAAAAAAAAAAAAA[-/A]CTATATGGGAGGATG	4297
rs11430367	in-del	-/TT	0	0	intron-variant	KMT2A	GRCh38.p7	11:118477524	TTTTTTTTTTTTTTT[-/TT]GAGACGGAGCCTCAT	4297
rs11436622	in-del	-/A/AA/AAA	0.480144	0.097642	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118517395	GTGAGACTCTGTCTC[-/A/AA/AAA]AAAAAAAAAAAAAAA	4297
rs11443977	in-del	-/A/AA/AAA	0	0	intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118519077	AAAAAAAAAAAAAAA[-/A/AA/AAA]GAAAATTAAACTTTA	4297
rs11445156	in-del	-/T	0.497641	0.0342639	intron-variant	KMT2A	GRCh38.p7	11:118486375	TGGTTTTTTTTTTTT[-/T]AATCTTTCTGAGTTT	4297
rs11552438	snp	G/T	0	0	missense, intron-variant	KMT2A	GRCh38.p7	11:118471701	GTGGGAGACCTAGAA[G/T]TGGCTCTGACCGAAA	4297
rs11552439	snp	A/G			missense, intron-variant	KMT2A	GRCh38.p7	11:118473360	CAGGAGTATCCAATA[A/G]AAAAAAAAAAAAAAA	4297
rs11825131	snp	C/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118479483	CAGTTGGGAGAAATG[C/T]TACATTATTTACTTC	4297
rs11825985	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118486603	CCACgtcgggtgcag[G/T]ggctcacgcctgtaa	4297
rs11826676	snp	A/G	0	0	upstream-variant-2KB, downstream-variant-500B, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118526863	TTTTGGCTTTGGTTG[A/G]AGAGGGTGGAGAAAA	4297
rs12226470	snp	G/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118453798	TATTCCCATTTCATA[G/T]GCAAGGAAACACATA	4297
rs12273879	snp	A/C	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118437680	AGCAGTCTCTTCCCC[A/C]CCCCGCCCCGTCTTA	4297
rs12283467	snp	A/C	0.00318978	0.0398085	intron-variant	KMT2A	GRCh38.p7	11:118465946	GTAACATTGTAGCCT[A/C]CAAGTGTAAACCCTG	4297
rs12287684	snp	A/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118462932	TTAATGCTTCCTGTC[A/T]TTTTGGAAAGTACTT	4297
rs12363882	snp	C/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118443942	TTTTGATGTCTTTCA[C/G]CAACAAAAGATATGA	4297
rs12574896	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118454838	actttAAAAAAATGG[G/T]taatttttttttttt	4297
rs12577103	snp	A/C	0	0	intron-variant	KMT2A	GRCh38.p7	11:118492273	aaggactggagacac[A/C]tgagcctagaggcag	4297
rs12795374	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118453224	atttctactttctca[C/T]ctttcattctttcct	4297
rs12795384	snp	C/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118453229	tactttctcaccttt[C/T]attctttcctcaact	4297
rs12795394	snp	A/C	0	0	intron-variant	KMT2A	GRCh38.p7	11:118453238	acctttcattctttc[A/C]tcaactactccagtt	4297
rs12795408	snp	C/T	0.173568	0.23803	intron-variant	KMT2A	GRCh38.p7	11:118453264	cagttgggcttttat[C/T]cccatgatgcctctg	4297
rs12796769	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118453197	tccttgaaagtgctg[G/T]gtgtaattgctattt	4297
rs17122239	snp	C/T	0.0741063	0.177655	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520687	ATTTTATAAGGCACT[C/T]GTTCAGTTTGGCATT	4297
rs34034814	in-del	-/C			intron-variant	KMT2A	GRCh38.p7	11:118444230	AAATATTTACACATG[-/C]CCCATATTCAACTTC	4297
rs34036506	in-del	-/T			frameshift-variant	KMT2A	GRCh38.p7	11:118509159	CTGTTCTTCCGGAAG[-/T]TCAGGTGACCCAAAA	4297
rs34112535	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118499074	TTTTGAATTATTTCG[-/A]AATGCAAAAGAAAAA	4297
rs34166714	in-del	-/A/AA			intron-variant	KMT2A	GRCh38.p7	11:118439159	AAAAAAAAAAAAAAA[-/A/AA]GAAAAAAAAGAAAAA	4297
rs34206138	in-del	-/G			intron-variant	KMT2A	GRCh38.p7	11:118451480	CAACCTCCACCTCCT[-/G]GGGCTCAAGTGATTC	4297
rs34234946	in-del	-/G			intron-variant	KMT2A	GRCh38.p7	11:118454441	CTACTCCACCAAGGT[-/G]CTTTATATGTCTGAC	4297
rs34239485	in-del	-/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512729	TCCAAAGTGGCTATA[-/G]CCATTTTACATTTCC	4297
rs34249563	in-del	-/C			intron-variant	KMT2A	GRCh38.p7	11:118478945	ATTTCTTTTTTTAAG[-/C]AAGTTTTGTTTTAAT	4297
rs34285672	in-del	-/T			intron-variant	KMT2A	GRCh38.p7	11:118495666	GGTATACTGTAGGAG[-/T]TCAATAAATGCTTGT	4297
rs34325355	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118495519	AAGAGTCATATGTTG[-/A]AGATATTTTTTAAAA	4297
rs34333194	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118495530	GTTGAGATATTTTTT[-/A]AAAATATTGAGTTCT	4297
rs34341404	in-del	-/G			intron-variant	KMT2A	GRCh38.p7	11:118483109	TGGTAGTGGGTGCTT[-/G]GTAATCCTAGCTACT	4297
rs34361700	in-del	-/T			intron-variant	KMT2A	GRCh38.p7	11:118481117	ATACTCTTGTAATTA[-/T]TTTTAAGGGTACAGT	4297
rs34434225	in-del	-/G			frameshift-variant	KMT2A	GRCh38.p7	11:118505084	TCTCAGATTTCCAAT[-/G]GCAGCTGTCCAGACC	4297
rs34449460	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118495603	TTCTGTGAATGGCTC[A/C]TACATGGGGCAACAG	4297
rs34465772	in-del	-/T			upstream-variant-2KB	KMT2A	GRCh38.p7	11:118435340	CCCTAACTCGCCTCC[-/T]TTCTTTCCCCCTCCC	4297
rs34527196	in-del	-/G			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118523341	CAAGGCCCACAACTT[-/G]GGGGACTAGACCACC	4297
rs34541939	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118483437	ACTCAGGAGAGTGAG[C/G]CAGGAGAATGGCGTG	4297
rs34601576	in-del	-/T			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522254	TTTCCAGCAGCTGGG[-/T]AGCTCCCGGATTGCG	4297
rs34683702	snp	A/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512713	TACTGCCAGGTTTTT[A/T]TTCCAAAGTGGCTAT	4297
rs34737216	in-del	-/G			intron-variant	KMT2A	GRCh38.p7	11:118492147	TACAATGAGAAATTT[-/G]GGACTTCATACTCTG	4297
rs34850700	in-del	-/G			intron-variant	KMT2A	GRCh38.p7	11:118447536	TTGAAAGCGATGTTA[-/G]GGGTATCCTGATGGG	4297
rs34854073	in-del	-/T			frameshift-variant, intron-variant	KMT2A	GRCh38.p7	11:118472244	AGTTAGGATTATTCC[-/T]TTCTTCAAAAAGGAC	4297
rs34926267	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118514461	TTTTTTTTTCTCCAA[A/G]ACAGAGTCTTACTCT	4297
rs34947643	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118458829	TTATCGCTGCCAAGA[-/A]TGCACAGTTTGCCTC	4297
rs34995086	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118444560	AGCTCAGCCATCTTG[-/A]AAAAGTTTTTTTTGT	4297
rs35006387	in-del	-/T			intron-variant	KMT2A	GRCh38.p7	11:118495548	ATATTGAGTTCTGTG[-/T]TACTTCAGCAATTTT	4297
rs35006880	in-del	-/T			intron-variant	KMT2A	GRCh38.p7	11:118447553	GGTATCCTGATGGGA[-/T]GGCATTATCTTTTAT	4297
rs35085183	in-del	-/G			upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118526039	AAAGCCTAGTTCAGT[-/G]CCATGGCTTTTAATT	4297
rs35148798	in-del	-/T			intron-variant	KMT2A	GRCh38.p7	11:118462498	AGAAATCAATCAATA[-/T]TTTCAAGTGCAAAGA	4297
rs35278914	in-del	-/C			frameshift-variant	KMT2A	GRCh38.p7	11:118500991	GTTTACCCAGGTGTT[-/C]CCAGGGTATACTGGA	4297
rs35304075	in-del	-/T			intron-variant	KMT2A	GRCh38.p7	11:118460335	CTCTGTCACCCAGGC[-/T]TGGAGTGCAGTGGCA	4297
rs35335315	in-del	-/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118513894	GTGAGCCAAGATTAT[-/G]GGCACTGCACTCCAG	4297
rs35367335	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118459843	GGCGGGCACTACCAC[-/A]GCCCGGCTAATTTTT	4297
rs35388308	in-del	-/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118515138	GCTGAGAAAGCTGAA[-/T]TTTTTAACATGTGCC	4297
rs35403836	in-del	-/T			intron-variant	KMT2A	GRCh38.p7	11:118443670	AGAGTTAGTTGGCAG[-/T]TTTTGTGTGCAGTGT	4297
rs35416851	in-del	-/T			intron-variant	KMT2A	GRCh38.p7	11:118495522	AGTCATATGTTGAGA[-/T]TATTTTTTAAAATAT	4297
rs35483459	in-del	-/A	1.76484e-05	0.0029705	intron-variant	KMT2A	GRCh38.p7	11:118490256	TTGCTAAAGGTACCC[-/A]AAAAAGCCAGTTTTG	4297
rs35487583	in-del	-/C			intron-variant	KMT2A	GRCh38.p7	11:118463289	AATAACTTTTTATTA[-/C]CCTGTTGAATACTTT	4297
rs35544096	in-del	-/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118516659	TGTCTGGCACAGTGG[-/G]AAAGATGGAAAGAGT	4297
rs35547365	in-del	-/T			intron-variant	KMT2A	GRCh38.p7	11:118495497	ATTTGTTTCAGCAAG[-/T]TTTAACCAAGAGTCA	4297
rs35564663	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118464539	GGGAAACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	4297
rs35581948	in-del	-/G			frameshift-variant	KMT2A	GRCh38.p7	11:118505054	GTGCCCAATTCTACT[-/G]GATAGTCCTGGCCCG	4297
rs35617664	in-del	-/T			intron-variant	KMT2A	GRCh38.p7	11:118495645	ATTTATTTTATACAG[-/T]TTCTAGGTATACTGT	4297
rs35626068	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118509516	TTTTTAGTTGTTACT[-/A]AAAGAAAACTAAGAA	4297
rs35633621	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118508726	GTGAGAACCTATCTC[-/A]AAAAAAAAAAAAAAA	4297
rs35644493	in-del	-/G			intron-variant	KMT2A	GRCh38.p7	11:118458935	TATATAATGGTACTA[-/G]GAAGCCTTCAAAACA	4297
rs35648788	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118508945	GGTAAAGAATCTCAC[A/C]AAAGAGTTTTATGTT	4297
rs35666931	in-del	-/T			intron-variant	KMT2A	GRCh38.p7	11:118495458	ACCATGCCCGGCCTC[-/T]TTTTGAGTTTTTGAT	4297
rs35685990	in-del	-/C			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118514469	TCTCCAAGACAGAGT[-/C]TTACTCTGTCACCCA	4297
rs35708132	in-del	-/G			intron-variant	KMT2A	GRCh38.p7	11:118508410	TATTGATATACATTT[-/G]GGATTGTTTCCAGAA	4297
rs35722104	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118495511	GTTTAACCAAGAGTC[-/A]ATATGTTGAGATATT	4297
rs35729146	in-del	-/T			intron-variant	KMT2A	GRCh38.p7	11:118495587	TGACTTGTTCTTATA[-/T]TTCTGTGAATGGCTC	4297
rs35733051	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118441367	GTTTTCGTTGTGTGG[-/A]AAAAACATAAGGACT	4297
rs35778255	in-del	-/A			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520355	AGTACTATATATACT[-/A]AAAATGGGACTCATT	4297
rs35780241	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118483232	GCTAGACTCCATCCC[-/A]AAAAAAAAAAAAAAA	4297
rs35921372	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118454809	AGTTTTCATGTACAC[-/A]AAATATTCTTTTGAC	4297
rs35939041	in-del	-/C			intron-variant	KMT2A	GRCh38.p7	11:118495100	ACTGCTCTTGATTTT[-/C]CCATATGTAACCTTT	4297
rs35961379	in-del	-/G			intron-variant	KMT2A	GRCh38.p7	11:118452395	AGAATAACCAGGCAT[-/G]GGTGGTGAGCACTGT	4297
rs36001121	in-del	-/C			intron-variant	KMT2A	GRCh38.p7	11:118495556	TTCTGTGTACTTCAG[-/C]CAATTTTCAAACGCT	4297
rs36001785	in-del	-/T			intron-variant	KMT2A	GRCh38.p7	11:118508807	AAGCCAGCTTACTTA[-/T]TTTAAGTAACTTTAG	4297
rs36026884	snp	C/T	0.00113624	0.0238082	synonymous-codon	KMT2A	GRCh38.p7	11:118502591	CTCAGTCTCCACCAC[C/T]GGGACCGCTACTGAT	4297
rs36029035	in-del	-/C			intron-variant	KMT2A	GRCh38.p7	11:118466905	ACTGTAAAAAGTACT[-/C]CCAGTAAGCCAGGCA	4297
rs36083173	in-del	-/G			frameshift-variant	KMT2A	GRCh38.p7	11:118503627	CCCAACCAAGCCCCA[-/G]ATAATACCTCATGCC	4297
rs55744803	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118513455	AGAGGGAAGGGAAGG[A/G]AAATATTTGGATGCA	4297
rs56156715	snp	C/T	0.00676609	0.0577691	intron-variant	KMT2A	GRCh38.p7	11:118477610	CTTCCCAGGTTCAAG[C/T]GATTCTCCTGCCTCA	4297
rs57102960	in-del	-/AA			intron-variant	KMT2A	GRCh38.p7	11:118498565	AAAAAAAAAAAAAAA[-/AA]GACTTTTTTAGAGCA	4297
rs57210324	snp	A/G			upstream-variant-2KB	KMT2A	GRCh38.p7	11:118434925	CAGTGGAGGGACGTA[A/G]GTTTTCAGCACCAGG	4297
rs57606175	snp	A/G	0.0584853	0.160693	intron-variant	KMT2A	GRCh38.p7	11:118464846	TTTTGGGGATGCTCA[A/G]GGCATTTTGCTTGTT	4297
rs57817005	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118456269	CTTTGGGAGGATTGC[A/T]TGAGCTCAGGAGTTT	4297
rs57883256	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118511088	ACCTTGAGGACTTTG[A/G]AAACTTGAGGGAGTG	4297
rs57898717	in-del	-/T	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118453412	TGGATTTTTTTTTTT[-/T]AACATTGTACTCACC	4297
rs58195630	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118466407	AGCAGTCCTCCCATA[C/T]TGGCCTCTCAAGGCG	4297
rs58201978	snp	C/T	0.00478085	0.0486577	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118516086	TTAACCACAATGACC[C/T]TTGTGTTCCCCAGTC	4297
rs58723753	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118489390	GGATGACTGTGCTTA[A/G]AGTATTGCTTTCTTT	4297
rs58992225	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118509302	ATTTAAAAAAAAAAA[-/A]TCTAAGCTCCAAAGA	4297
rs59281381	in-del	-/T			intron-variant	KMT2A	GRCh38.p7	11:118482329	TTTTTTTTTTTTTTT[-/T]CTAATGGCCCTTTCT	4297
rs59473145	in-del	-/A	0	0	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118517412	AAAAAAAAAAAAAAA[-/A]GAAAAGAAAAGAAAA	4297
rs59634120	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118510891	TTTGGGTTAGGCAAA[A/G]AAGAATGCAGGGCTC	4297
rs59752221	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118466387	GCCTTGAACTCCTGG[C/G]CTCAAGCAGTCCTCC	4297
rs59939662	snp	C/T			missense, intron-variant	KMT2A	GRCh38.p7	11:118473687	GGTTTACCCCAGGCT[C/T]TCAGACTGAAAGAGG	4297
rs59972810	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118482766	ACAAAAAAAAAAAAA[-/A]GAAGAAGAAGAAGAA	4297
rs60026549	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118456274	GGAGGATTGCTTGAG[C/G]TCAGGAGTTTCAGAC	4297
rs60200569	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118456263	CCAGCACTTTGGGAG[A/G]ATTGCTTGAGCTCAG	4297
rs60560012	in-del	-/AGTTCAAGACCAGC			intron-variant	KMT2A	GRCh38.p7	11:118482716	CAGTTCAAGACCAGC[-/AGTTCAAGACCAGC]CTGGGCAACATAGCA	4297
rs60572091	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118467689	TTTTAAATTAACTGA[A/G]AAAATAATCCTTCAG	4297
rs61084765	in-del	-/A			upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118525602	CTTGATTTAAAAAAA[-/A]TAAAAAATAAAAAAA	4297
rs61370062	snp	G/T	0.0263992	0.111815	intron-variant	KMT2A	GRCh38.p7	11:118495146	AAATTCTTTTGATTT[G/T]ATTTTATTTATTTAT	4297
rs61513148	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118456285	TGAGCTCAGGAGTTT[C/G]AGACCAGCCTGGGCA	4297
rs61751531	snp	C/T			synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473112	AATATTTGATAATTT[C/T]CGACCCCCTCCACTA	4297
rs61752725	snp	A/G			synonymous-codon	KMT2A	GRCh38.p7	11:118504460	CATTATGGACTTTGT[A/G]CTAAAGAATACTCCA	4297
rs61900940	snp	A/G	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118445919	TGAGGCAGGAGAATC[A/G]CCTGAACCCAGGAGG	4297
rs61900941	snp	C/T	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118457256	ATGATACACCTCCTG[C/T]CTTTTTTTTTTTTTT	4297
rs61900942	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118457432	CCACCACGCCTGGCT[A/T]ATTTTTTTTTTGTAT	4297
rs61900943	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118460445	GCATGCACCAGCACA[C/T]CCAGCTATTTTTTTG	4297
rs61900944	snp	A/G	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118482798	TTAGCCAGGCATGGT[A/G]GCAGTTGCGTGTAGT	4297
rs61900945	snp	A/C	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118483230	AGAGCTAGACTCCAT[A/C]CCAAAAAAAAAAAAA	4297
rs61900946	snp	C/T	0.5	0	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521037	TGGGATCCTGCACCT[C/T]CTTGTGTTGAACAAG	4297
rs66869191	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118497880	AAGCTAATGCCGAGG[-/A]AAACCTCCTTTGGCA	4297
rs67179230	in-del	-/T	0	0	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118515683	TTTTTTTTTTTTTTT[-/T]GAGACAGGGTCTCAC	4297
rs67392231	in-del	-/T			frameshift-variant, intron-variant	KMT2A	GRCh38.p7	11:118473197	TCAGCCCGATTGTTT[-/T]CGCCACTCCATTCTG	4297
rs67796916	in-del	-/A	0	0	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118518796	AAAAAAAAAAAAAAA[-/A]GCCGGGCGCGGTGGC	4297
rs71469178	in-del	-/T	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118476202	GAGCCACCACCTATA[-/T]CTTTCATTTATAAGT	4297
rs71469179	in-del	-/T	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118476206	CCACCACCTATACTT[-/T]CATTTATAAGTTATT	4297
rs71469180	in-del	-/A/G	0.5	0	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118513958	AAAAAAAAAAAAAAA[-/A/G]GAAAAAGAAAAAAAA	4297
rs71482145	snp	A/G	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118477692	TTTGTATTTTTAGTA[A/G]AGAGGGGTTTTGCTA	4297
rs71482146	snp	A/G	0.5	0	missense	KMT2A	GRCh38.p7	11:118477990	TCAATTGCTGGCTCA[A/G]AAGATGCTGAACCTC	4297
rs71482147	snp	A/C	0.5	0	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118515027	CCACCTCGGCCTCCC[A/C]AAGTGCTGGGATCAC	4297
rs71482148	snp	C/T	0.5	0	synonymous-codon, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522164	AAATGCCGGAAGTTC[C/T]TAAACTAAAGCTGCT	4297
rs72218407	in-del	-/T			intron-variant	KMT2A	GRCh38.p7	11:118463124	TTACATTTATCTTTA[-/T]TTTTTTTTTTTTAAA	4297
rs72371994	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118489232	TGAGACTCCATCTCA[-/A]AAAAAAAAAAAAAAA	4297
rs73020226	snp	A/C	0.0174175	0.0916809	intron-variant	KMT2A	GRCh38.p7	11:118452209	CTACGTCTGGCTCTG[A/C]ATCAGGAGATTTTAA	4297
rs73022015	snp	G/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512803	ACTTACCTGTTTTTT[G/T]TTTTTTTTTTTTTAT	4297
rs73555267	snp	C/T	0.00517822	0.0506191	intron-variant	KMT2A	GRCh38.p7	11:118481656	GTGGCTCTGTAATTC[C/T]ATTTTAAATAAAATT	4297
rs73555280	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118493632	GATGCCTGTTAATTT[C/T]ATGATTTTAAGTATG	4297
rs73615905	snp	A/G	0.0509478	0.151255	intron-variant	KMT2A	GRCh38.p7	11:118448747	GGCATATAATGAATG[A/G]TCTCTACTTTTAACC	4297
rs73615908	snp	C/T	0.0509478	0.151255	intron-variant	KMT2A	GRCh38.p7	11:118451692	GAGATGGGGTCTCAC[C/T]ATCTTATGTAGCTGG	4297
rs73615909	snp	C/T	0.191147	0.242974	intron-variant	KMT2A	GRCh38.p7	11:118451773	CTGGGATTATAGGTG[C/T]GACCCACCATGCCCA	4297
rs74333120	snp	A/C	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118464539	AGGGAAACTCTGTCT[A/C]AAAAAAAAAAAAAAA	4297
rs74365173	snp	A/C	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118508723	GAGAACCTATCTCAA[A/C]AAAAAAAAAAAAAAG	4297
rs74387673	snp	A/G	0.000398651	0.0141126	intron-variant	KMT2A	GRCh38.p7	11:118491150	GGGCCGTAAAAACAC[A/G]GGTATGTGAGCCAAA	4297
rs74422681	snp	A/G	0.0984431	0.198823	intron-variant	KMT2A	GRCh38.p7	11:118442155	AACTGAAGGCCTTCA[A/G]TCGGGCCTTTTGTGA	4297
rs74613583	snp	A/G	0.00636936	0.0560724	intron-variant	KMT2A	GRCh38.p7	11:118442378	GCATGATGTACCTAC[A/G]TTTTAATCAGATTCT	4297
rs74713110	snp	C/T	0.0154538	0.0865337	intron-variant	KMT2A	GRCh38.p7	11:118499146	TGGTGTTCCTAGAGG[C/T]ACCACCTCTTTTGGG	4297
rs74765846	snp	A/T	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118484044	CTCTTTTAAAAAAAA[A/T]TTCAAAGATTATTTG	4297
rs74860701	snp	A/T	0.00835141	0.0640778	intron-variant	KMT2A	GRCh38.p7	11:118509450	ATACTCTTCTGCTGT[A/T]CTGGTTTTACCAGCA	4297
rs74891613	snp	A/C	0.000798403	0.0199641	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521515	TAGTGTATGTTATCA[A/C]TTCAGAGACCTTTCT	4297
rs75295603	snp	G/T	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118456339	TAAAAATTTAAAAAA[G/T]GAACCTTTTTTTTTT	4297
rs75350869	snp	A/T	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118451658	CCTCCCAAAGTGAAT[A/T]TTTTTTTTTTTTTTT	4297
rs75399345	snp	A/G	0.0165278	0.0893908	intron-variant	KMT2A	GRCh38.p7	11:118467902	TATCATTCTGTGTCT[A/G]TCTCTGGAAAGAACT	4297
rs75559225	snp	G/T	0.00716266	0.059414	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118514435	TTCCAGATCCATCCA[G/T]GTGTCTTTTTTTTTT	4297
rs75669268	snp	A/G	0.00676609	0.0577691	intron-variant	KMT2A	GRCh38.p7	11:118466943	GCATGTATGTAGTCC[A/G]AGCTATGCAGGAGGC	4297
rs75683916	snp	A/C			missense	KMT2A	GRCh38.p7	11:118504246	AGCCAAAGATGGATA[A/C]CTGCCATTCTGTAAG	4297
rs75687964	snp	A/C	0	0	intron-variant	KMT2A	GRCh38.p7	11:118483233	GCTAGACTCCATCCC[A/C]AAAAAAAAAAAAAAA	4297
rs75867055	snp	A/C	0.000662212	0.0181843	missense, intron-variant	KMT2A	GRCh38.p7	11:118471955	TCTGCTACGTTTCAG[A/C]AAGCCACAAAGATTA	4297
rs75970907	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118476648	GGATACAGTAATAGT[A/T]GATTTCTGTTTTGAT	4297
rs76035590	snp	A/G	0.0444908	0.142359	intron-variant	KMT2A	GRCh38.p7	11:118450380	GCAGGGTGGGTGGAG[A/G]TCACCTGTCTCATTT	4297
rs76062856	snp	A/T	0.444444	0.157135	intron-variant	KMT2A	GRCh38.p7	11:118495164	TTTATTTATTTATTT[A/T]TTTTTTTTTTTTTGA	4297
rs76091267	snp	G/T	0.0501905	0.150254	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512858	TATCTTTTCTTAAAG[G/T]TGAAATCATTTACCA	4297
rs76150240	snp	A/T	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118456338	CTAAAAATTTAAAAA[A/T]TGAACCTTTTTTTTT	4297
rs76167065	snp	C/T	0.00517822	0.0506191	intron-variant	KMT2A	GRCh38.p7	11:118487789	TTAGGTTTGACCAAT[C/T]GTCCCAATAATTCCT	4297
rs76196895	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118444290	AGATCAAACACAAAC[A/G]TTGTCCCTAGATTAT	4297
rs76243544	snp	A/C	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118482754	GTCTTTATTTAAACA[A/C]AAAAAAAAAAAAGAA	4297
rs76340122	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118476649	GATACAGTAATAGTT[A/G]ATTTCTGTTTTGATA	4297
rs76427799	snp	A/T	0.00874735	0.0655527	intron-variant	KMT2A	GRCh38.p7	11:118479445	GAATGAGTGAGTCAC[A/T]TGCAAGTGATTAATA	4297
rs76521734	snp	C/G	0.0107246	0.0724382	intron-variant	KMT2A	GRCh38.p7	11:118443031	GTTGAAGAAGGCCTG[C/G]GAGAAGGAAGTACAG	4297
rs76550494	snp	A/T	0.00597247	0.0543191	intron-variant	KMT2A	GRCh38.p7	11:118496684	TTGTGAAAGTTAATA[A/T]AATCTAAGTTGCATA	4297
rs76599408	snp	A/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118486720	TCTACTAAAAAAAAA[A/T]TAAAATACCAGGCAT	4297
rs76651078	snp	A/G	0.0693013	0.172766	intron-variant	KMT2A	GRCh38.p7	11:118445291	AAAAAAGAAGAAAGA[A/G]AACAAGATGGTAAAT	4297
rs76661490	snp	C/G/T	0.00914312	0.0669923	intron-variant	KMT2A	GRCh38.p7	11:118455002	CACCTCTCCACCCCC[C/G/T]ACTCCTGTCAATTCT	4297
rs76720717	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118438152	GTGTGGTGGCGGTGG[G/T]TGCTTTGGGATGGGA	4297
rs76721917	snp	C/G	0.000380332	0.0137848	missense	KMT2A	GRCh38.p7	11:118503196	AGAAAGGGAAAAAAT[C/G]CTGTAAAGAAACTTT	4297
rs76824622	snp	A/T	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118451655	CGGCCTCCCAAAGTG[A/T]ATTTTTTTTTTTTTT	4297
rs76849850	snp	A/G	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118501472	AGACTGTGTCTCAAA[A/G]AAAAAAAAAAAAAGA	4297
rs76962363	snp	G/T	0.00795532	0.062565	upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118526540	ATGTATAACAGATCT[G/T]TTTTTTTTCCTTGTG	4297
rs77069905	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118508999	GTTGTATTCATTCAA[C/T]AAGTTCTACAGAAAG	4297
rs77144326	snp	A/G	0.0329836	0.124112	intron-variant	KMT2A	GRCh38.p7	11:118445016	CACATAGGAAGCCCT[A/G]ATTGTTAGAACCAAG	4297
rs77157104	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118438149	TTAGTGTGGTGGCGG[G/T]GGTTGCTTTGGGATG	4297
rs77160873	snp	A/G	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118438602	GCCGTTGGTGCACAC[A/G]AAATATCCTGGGCAA	4297
rs77275625	snp	A/C			missense	KMT2A	GRCh38.p7	11:118494321	ATTGTGAAGATCATT[A/C]AAGCAGCCATTAATT	4297
rs77421119	snp	C/T	0.00205705	0.0320046	synonymous-codon	KMT2A	GRCh38.p7	11:118499350	AAGAGTGTTTGTGGA[C/T]TTTGAAGGAATCAGC	4297
rs77487830	snp	A/G	0.0402882	0.136092	intron-variant	KMT2A	GRCh38.p7	11:118441154	CAAAAGTCAGAGTCA[A/G]GTGAGACGATTTGAT	4297
rs77534835	snp	A/G	0.0260105	0.111035	intron-variant	KMT2A	GRCh38.p7	11:118466858	AAAAAAAGAACTTAC[A/G]TGTAAGAATTTAAAT	4297
rs77535829	snp	C/T	0.0379877	0.132479	intron-variant	KMT2A	GRCh38.p7	11:118440962	GTGGGCTCTCATCTC[C/T]GTTACTGAACAGTTA	4297
rs77546552	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118476228	TAAGTTATTTCACCC[C/G]TACTTCTCTGATGAT	4297
rs77554882	snp	A/C	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118449585	AGTGAGACTCCATCT[A/C]AAAAAAAAAAAAAAA	4297
rs77965158	snp	C/T	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118457258	GATACACCTCCTGCC[C/T]TTTTTTTTTTTTTTT	4297
rs78013188	snp	A/G	0.0221141	0.102801	intron-variant	KMT2A	GRCh38.p7	11:118441395	ACTTTGGGGAAGTTG[A/G]CCAGTTTCATTTATA	4297
rs78020509	snp	A/G	0.199873	0.244923	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118514096	ATAACTGAGTCTCCT[A/G]TCTCACCTCCTTGTA	4297
rs78025177	snp	G/T	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118467065	TAAATTTAGGTTTCA[G/T]ACATTCTTAGAATTA	4297
rs78112480	snp	C/T	0.0134861	0.0810011	intron-variant	KMT2A	GRCh38.p7	11:118453729	CTATATTCTGAGCAC[C/T]TCACATGAATTATCT	4297
rs78155594	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118454882	GCAGAACAATTGATG[G/T]TGGGCCAAATTCGGC	4297
rs78163701	snp	C/T	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118478660	TCTACTGAAATTATG[C/T]TGACCCAACAAAATT	4297
rs78316802	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118474635	ACTAAGGTTGGGACT[A/G]TATCACAGAGGATGC	4297
rs78375882	snp	A/G	0.00716266	0.059414	intron-variant	KMT2A	GRCh38.p7	11:118494613	TATCCTCGTATTAAC[A/G]GAGAAGCTGGTTTGA	4297
rs78394155	snp	A/C			stop-gained	KMT2A	GRCh38.p7	11:118504318	TCAGCTCATTGGAGT[A/C]AAGCCGCAGAGTCCA	4297
rs78418495	snp	A/T	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118486895	CCTGTCTCAAAAAAA[A/T]TTTTAAAAATTTAAA	4297
rs78558747	snp	A/G	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118494077	AGCCAATTTGTTTGC[A/G]TTCTTACCTCATTAG	4297
rs78590081	snp	C/T	1.8582e-05	0.00304806	intron-variant	KMT2A	GRCh38.p7	11:118490104	AACAAGAAATTCCTA[C/T]TGAATTTCTTTTCTT	4297
rs78761045	snp	C/T	0.00874735	0.0655527	intron-variant	KMT2A	GRCh38.p7	11:118476708	TGTGTGTTTTGATTC[C/T]AAATCATACTGAAAT	4297
rs78915574	snp	G/T	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118455087	GGTTGGAGCGCAGTG[G/T]CTCAGTCAGTTCACT	4297
rs78956418	snp	C/G	0.000798403	0.0199641	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520129	CAGCTGGTCAGGGCA[C/G]TACGTAGGAATTTGT	4297
rs79015640	snp	A/C	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118449587	TGAGACTCCATCTCA[A/C]AAAAAAAAAAAAAAA	4297
rs79111661	snp	A/T	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118509303	CATTTAAAAAAAAAA[A/T]TCTAAGCTCCAAAGA	4297
rs79275381	snp	C/G	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118509264	GGATTATGAGAATCA[C/G]CCACTTTACCTACTT	4297
rs79405108	snp	A/C			missense, intron-variant	KMT2A	GRCh38.p7	11:118471952	CCTTCTGCTACGTTT[A/C]AGCAAGCCACAAAGA	4297
rs79406650	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118526457	CAGGTAGTTGAATAA[C/T]TGTTTCAAGAGCTCA	4297
rs79587981	snp	A/G	0.00438332	0.0466095	intron-variant	KMT2A	GRCh38.p7	11:118447207	CGTATACCTTATGTC[A/G]TGGTACTTTTGAAAT	4297
rs79648960	snp	A/G	0.0142736	0.0832652	utr-variant-3-prime, intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118524909	CTAAACCCTGAGGAC[A/G]GGGGAGGAACCCACA	4297
rs79686126	snp	A/G	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118498564	TTAAAAAAAAAAAAA[A/G]AGACTTTTTTAGAGC	4297
rs79703183	snp	A/T			missense, intron-variant	KMT2A	GRCh38.p7	11:118472444	ACCCCTCGGCGGTTT[A/T]TAGAGGATGAGGATT	4297
rs80006690	snp	C/T	0.00358779	0.0422022	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118516290	CTTGATGAGGCAACA[C/T]TTGAGCTTAGACCTG	4297
rs80029483	snp	A/G	0.00874735	0.0655527	intron-variant	KMT2A	GRCh38.p7	11:118440195	CTTCTAAAACTAGGT[A/G]ACAGAACTTCCAGAT	4297
rs80320757	snp	G/T	0.00517822	0.0506191	intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118511534	TTCTGCCTCTTAACT[G/T]TAAGGAACAGAGAGG	4297
rs111274901	snp	C/G	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118478842	CTCACTGCCAACACT[C/G]AACTCCTAGGCTCCA	4297
rs111313792	snp	C/T	5.12702e-05	0.00506285	intron-variant, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118511927	ATATTTTCTGGCTTA[C/T]GGGTTTTCTTTATTT	4297
rs111321181	snp	A/G	0.5	0	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473337	AACTTCTGCTGGAAC[A/G]TCTTCTTCAGGAGTA	4297
rs111328758	snp	A/G	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118460024	TTAAGGGAGGAACTA[A/G]AAGCTATGCATTTTA	4297
rs111382006	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118453781	GTCTGAAGTATCACT[A/G]GTATTCCCATTTCAT	4297
rs111405302	snp	C/T	0.199254	0.244796	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118514976	GTTTCACCGTGCTGG[C/T]CAGGCTACTCTAGAA	4297
rs111411364	snp	A/C	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118438744	CATTTTTTAGTTGTT[A/C]GTCTTCCTGCCTCCT	4297
rs111444752	snp	C/T	1.64917e-05	0.00287151	synonymous-codon	KMT2A	GRCh38.p7	11:118502873	TGCACATAATGTGGC[C/T]TACCCTGGAATTCCT	4297
rs111619412	snp	G/T	0.0517044	0.152246	intron-variant	KMT2A	GRCh38.p7	11:118467195	CAACCTGCCCAACAT[G/T]GTAAAACCCTGTCTC	4297
rs111765539	snp	C/T	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118494678	ATATTTACATTTTGT[C/T]TGTGTTTTCTTTTAG	4297
rs111782402	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118454001	TTATTCACATCTCAC[A/G]TCTATCCCATCAGCA	4297
rs111872936	snp	A/C	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118499714	GAACCCCGGAGGCAG[A/C]GGCTGCAGTGAGCTG	4297
rs111901186	snp	A/G	0.164546	0.234942	intron-variant	KMT2A	GRCh38.p7	11:118457337	CAGTGGCATGATCTT[A/G]GCTCACTGCAACCTC	4297
rs111903103	snp	C/T	0.0333695	0.124785	intron-variant	KMT2A	GRCh38.p7	11:118437784	ATGAAGGATTAGTGG[C/T]ATCTTGGAGGGGAAA	4297
rs111910322	snp	G/T	0.5	0	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522798	TGAGCCTGCAGGCTT[G/T]GAGTGGGAGTGTTGC	4297
rs111997050	snp	C/T	0.0678174	0.1712	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118517177	GAGGTGGGCAGATCA[C/T]GAGGTCAGGAGATCG	4297
rs112089616	snp	C/G			missense	KMT2A	GRCh38.p7	11:118504114	CAACAAGGAAAAGCA[C/G]CCAGATTCCAAAAAG	4297
rs112123832	snp	C/T	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118497753	ATGGAAAAAGTAATC[C/T]TGAAAAGAAGGAAGT	4297
rs112133791	snp	A/G	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118509834	AAATGGGAATAATAA[A/G]CCAACTGTGGAATGT	4297
rs112170961	snp	A/G	0.5	0	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521099	TGCTTCCAGCGGGTC[A/G]CAGAATGGAAATAAC	4297
rs112203672	snp	A/C	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118484364	TGTCAAAGACTTTAA[A/C]TAAAGAAAATGCTAC	4297
rs112508300	snp	A/G	0.0325976	0.123435	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118514534	CAACCTCCATCTCCC[A/G]GGTTCAGGTGATTCT	4297
rs112584352	snp	C/T	0.00111617	0.0235974	intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118511907	ATTAAGAAGGGTTTA[C/T]GTGCATATTTTCTGG	4297
rs112636863	snp	C/T	0.16028	0.233346	intron-variant	KMT2A	GRCh38.p7	11:118462795	TCTCGATCTCCTGAC[C/T]TTGTGATCCTCCCAC	4297
rs112673709	snp	C/G	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118446342	GGATAGAGTGAGACT[C/G]TGTCTCAAAAGAAAG	4297
rs112678346	snp	A/G	0.00154732	0.0277717	missense	KMT2A	GRCh38.p7	11:118506288	CTCCTTGCCAGCAAA[A/G]CTGGGATTCATTCTT	4297
rs112836014	snp	A/G/T	1.65548e-05	0.002877	synonymous-codon	KMT2A	GRCh38.p7	11:118490164	CTGTAAGAGCTGTGG[A/G/T]TCCACAACTCCAGGC	4297
rs112883141	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118483384	AAAAATACAAAAAAA[A/T]TAGCCCGGCGAGGTG	4297
rs112900272	snp	C/T	0.0696718	0.173152	intron-variant	KMT2A	GRCh38.p7	11:118455730	TGAGGCAGGGTCTCA[C/T]TCTGTTATCCAGGCT	4297
rs112915987	snp	C/T	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118497886	ATGCCGAGGAAAACC[C/T]CCTTTGGCATTATAT	4297
rs112956609	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118483383	TAAAAATACAAAAAA[A/T]TTAGCCCGGCGAGGT	4297
rs113003878	snp	A/T	0.5	0	missense	KMT2A	GRCh38.p7	11:118509949	TTTCTCCCTATTAGA[A/T]CCTAAAACAGTGGAA	4297
rs113028342	snp	A/G	0.0693013	0.172766	intron-variant	KMT2A	GRCh38.p7	11:118462822	CCACGTCGGCCTCCT[A/G]AAGTCCTGGGATTAC	4297
rs113048560	snp	C/T	0.00199481	0.0315187	intron-variant	KMT2A	GRCh38.p7	11:118496430	AACTGTTTGTCCTTG[C/T]GTCCATACTTGATGA	4297
rs113051825	in-del	-/AG	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118509343	TTTGGCCCACATTGG[-/AG]ACTGAAACTTGGCGC	4297
rs113097773	snp	A/G	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118478839	TAGCTCACTGCCAAC[A/G]CTGAACTCCTAGGCT	4297
rs113123703	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118457479	GGTTTCACCATGTTG[C/G]CCAAGCTGGTCTCAA	4297
rs113126135	snp	G/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118514791	GGCATGTGCCACCAT[G/T]CCTGGCTAATTTTGT	4297
rs113164907	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118476526	TGTAGAGATGGGTTC[C/T]CGCTATGTTGCCCAT	4297
rs113171016	snp	C/T	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118489692	CTCATAATTGTGTGC[C/T]GTACTTACTTGCCAG	4297
rs113178411	snp	C/T	1.64827e-05	0.00287073	synonymous-codon	KMT2A	GRCh38.p7	11:118503764	TCCCCGTCGCAGTGC[C/T]CGTGCACGTTCTAAC	4297
rs113302539	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519433	TCACAAACATTTTCC[A/G]TATTGATAGATCTGT	4297
rs113302674	snp	A/G	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118494671	TGTTTACATATTTAC[A/G]TTTTGTTTGTGTTTT	4297
rs113303920	in-del	-/A	0	0	intron-variant	KMT2A	GRCh38.p7	11:118495628	CAACAGGTGATATCA[-/A]GAATTTATTTTATAC	4297
rs113399762	snp	C/T	0.153997	0.230832	intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118518983	CTCGGGAGGCTGAGG[C/T]AGGAGAATGGCGTGA	4297
rs113464589	snp	C/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118510636	TTGTTTTGTCCGTGT[C/T]TGTTTACTTTTATCA	4297
rs113515064	snp	A/G	0.5	0	missense	KMT2A	GRCh38.p7	11:118505737	TTAATACTTCATCTC[A/G]CCGAACTGTCCCCAA	4297
rs113523063	snp	A/G	0.000148506	0.00861575	synonymous-codon	KMT2A	GRCh38.p7	11:118489869	CCCCACCAAACCCAC[A/G]AAGAAGAAGAAAGTC	4297
rs113546126	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118493777	TGCAGTGACATGATC[C/T]CGGCTCACTGCAACC	4297
rs113566564	snp	A/G	0.0693013	0.172766	intron-variant	KMT2A	GRCh38.p7	11:118464432	CCCAGCTACTTGGGA[A/G]GTTGAGACAGGAGAA	4297
rs113571925	snp	G/T	0.5	0	intron-variant	KMT2A	GRCh38.p7	11:118470150	CTTCTCTGTTCTGCT[G/T]CTTCTACTTATCTAC	4297
rs113814572	snp	A/C/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118500906	GGCCAGGGAACCTAG[A/C/G]ATAAAGAGAGGTTTT	4297
rs114103497	snp	A/C	0.00795532	0.062565	intron-variant	KMT2A	GRCh38.p7	11:118508069	AACAAGTAAACAAAA[A/C]ATATAACAAGAATTA	4297
rs114256097	snp	G/T	0.00398564	0.0444627	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118516121	ACCTGTCCATTATAC[G/T]CCATTTCCAGTGCTG	4297
rs114256542	snp	A/C	0.0023933	0.0345097	intron-variant	KMT2A	GRCh38.p7	11:118470572	AAAGGAGCTGTGAAT[A/C]CTTAATCTATTAAAG	4297
rs114451765	snp	G/T	0.0193772	0.0965046	intron-variant	KMT2A	GRCh38.p7	11:118480713	TGTCTTTCAGGCTGG[G/T]GTGCAGTAGCATGAT	4297
rs114816148	snp	A/G	0.0119091	0.0762411	intron-variant	KMT2A	GRCh38.p7	11:118495034	TACAGCCATGTAGCT[A/G]GCCTTGTTATAAATG	4297
rs114864896	snp	C/T	0.0174175	0.0916809	intron-variant	KMT2A	GRCh38.p7	11:118475440	TTGTAATGTTATTCA[C/T]GGGCTGGGTACGGTG	4297
rs114964540	snp	G/T	0.0170251	0.090679	intron-variant	KMT2A	GRCh38.p7	11:118440595	CACAAAATATTAAAA[G/T]CAAAATTTCCATCCT	4297
rs114968644	snp	A/G	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118489739	TACTAAGTAATAGGT[A/G]TTGGGTGAAGGTAAT	4297
rs115083416	snp	A/T	0.00795532	0.062565	intron-variant	KMT2A	GRCh38.p7	11:118448179	AGAGAAATCTTAAAC[A/T]TCAAGAGAAACCAAG	4297
rs115278894	snp	C/T	0.0221141	0.102801	intron-variant	KMT2A	GRCh38.p7	11:118439401	CATTCCAAATATTAT[C/T]ACATATTCAAAAGCA	4297
rs115378027	snp	A/G	0.0325976	0.123435	intron-variant	KMT2A	GRCh38.p7	11:118457229	AACTCATGAAGGCAT[A/G]TAAGACCTTTCATGA	4297
rs115427385	snp	A/G	0.0126979	0.078662	intron-variant	KMT2A	GRCh38.p7	11:118441275	CTGGGATTCTGTTTG[A/G]TAATTTTTAATATCA	4297
rs115463365	snp	C/T	0.00874735	0.0655527	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118515969	CTGAGAGTACAGGTA[C/T]CCAGCCCCATGTCCA	4297
rs115492534	snp	A/G	0.0205511	0.0992634	intron-variant	KMT2A	GRCh38.p7	11:118495105	CTCTTGATTTTCCAT[A/G]TGTAACCTTTAATTT	4297
rs116075212	snp	C/T	0.00755907	0.0610114	intron-variant	KMT2A	GRCh38.p7	11:118442685	AGGAGGTTCTGGAAA[C/T]TGTTGAGTTAATTAA	4297
rs116213038	snp	A/G	0.00398564	0.0444627	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118513993	TGCTCATAATTTTTA[A/G]AATTCTACCCCAAAA	4297
rs116840060	snp	A/G	0.00517822	0.0506191	intron-variant	KMT2A	GRCh38.p7	11:118498600	TAGGTTCACAGCAAA[A/G]TTGACTGGAAGGTAC	4297
rs116900309	snp	A/G	0.00716266	0.059414	intron-variant	KMT2A	GRCh38.p7	11:118439902	AACCTCTGAGCTGGT[A/G]GTTTTCAGTGTAGAA	4297
rs116954303	snp	A/G	0.00636936	0.0560724	intron-variant	KMT2A	GRCh38.p7	11:118455503	CAGTCTGTATTCATT[A/G]CATTTGCTTTGACCA	4297
rs117099452	snp	A/G	0.00348735	0.0416114	missense	KMT2A	GRCh38.p7	11:118506210	ACTCAGACTACGGGC[A/G]TAACAGCCGCTTCAC	4297
rs117484600	snp	C/T	0.00716266	0.059414	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118513430	TTTTATCAGTGATGT[C/T]CTTCCTTTAAGAGGG	4297
rs117511344	snp	A/G	0.00318978	0.0398085	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118516214	TGAAGAAGATAACAT[A/G]GGGAAATGAAATAGA	4297
rs117567821	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118460050	TTTTAGTTGGGGATA[A/G]GGAAGAAAACATTAC	4297
rs117692849	snp	C/T	0.00358779	0.0422022	utr-variant-3-prime, intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118525018	CCTCTTCTAGCTCAG[C/T]CTTGAGTCCATTGCC	4297
rs117748193	snp	C/T	0.0162398	0.0886349	intron-variant	KMT2A	GRCh38.p7	11:118449446	AAAATTAGCCAAGCA[C/T]GGTGGCCTGGCGCCT	4297
rs117787306	snp	A/G	0.0023933	0.0345097	intron-variant	KMT2A	GRCh38.p7	11:118511188	GAGATGCTCAAAGAC[A/G]AGAGTTTACTAATGA	4297
rs118171488	snp	A/T	0.00279162	0.0372561	intron-variant	KMT2A	GRCh38.p7	11:118443510	AAGAATTTTGTTACG[A/T]GATTTGTAATTGTTG	4297
rs137867090	snp	A/G	3.29489e-05	0.00405874	missense, intron-variant	KMT2A	GRCh38.p7	11:118472985	TGCAAGGGAAGCGAA[A/G]ATCTATTTTGCGAGA	4297
rs137888966	snp	A/G	0.0103295	0.0711199	intron-variant	KMT2A	GRCh38.p7	11:118451712	TATGTAGCTGGTCTC[A/G]AACTCCCAGGCTCAA	4297
rs138022952	snp	C/T	0.00133543	0.0258057	intron-variant	KMT2A	GRCh38.p7	11:118498085	GCTGGTAAGACCTTA[C/T]GGGTAAATTTTATGA	4297
rs138046203	snp	C/T	6.59022e-05	0.00573993	synonymous-codon	KMT2A	GRCh38.p7	11:118505661	GTTTCTAATATGACA[C/T]TGATTAACTTCACAC	4297
rs138095222	snp	C/T	0.00716266	0.059414	intron-variant	KMT2A	GRCh38.p7	11:118475181	TTAGAAGCACTTAGC[C/T]TTGAGCCATGGAACA	4297
rs138154606	snp	C/T	0.00279162	0.0372561	intron-variant	KMT2A	GRCh38.p7	11:118453427	TAACATTGTACTCAC[C/T]TGTTTTTCTTCTTAA	4297
rs138177395	snp	A/G	0.0174175	0.0916809	intron-variant	KMT2A	GRCh38.p7	11:118475928	TCTTTTTTTTGAGAC[A/G]GAATTTCGCTCTTGT	4297
rs138194391	snp	C/T	0.00318978	0.0398085	intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118519382	AAGCAAAATAGTCCA[C/T]AGTTTGGTGGCATGC	4297
rs138256365	in-del	-/T	0.0170251	0.090679	intron-variant	KMT2A	GRCh38.p7	11:118496786	ATTTCTGTGCTTAAC[-/T]GCCTACTTATTGACT	4297
rs138422538	snp	A/G	0.00557542	0.0525036	intron-variant	KMT2A	GRCh38.p7	11:118493803	CAACCTCTGCCTCCC[A/G]TAATCAAGTGATTCT	4297
rs138446387	snp	A/G	1.65718e-05	0.00287848	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118471738	TATCCTCTCAGATCC[A/G]TCTGTGTTTTCCCCT	4297
rs138509283	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118480857	TTTTTTGCAGAGACA[C/T]GATTTTGCCATGTTG	4297
rs138521226	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118435657	GTGGCCTCAGTGCCC[C/G]GGCTGGAGAAACACA	4297
rs138551362	snp	A/G	0.000153988	0.00877328	missense	KMT2A	GRCh38.p7	11:118507609	GTGGGCAACCTGCAG[A/G]GTAAGCTGAAGAATT	4297
rs138598543	snp	A/T	1.65507e-05	0.00287664	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473340	TTCTGCTGGAACATC[A/T]TCTTCAGGAGTATCC	4297
rs138702558	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118452236	TTAAATGTTCTCAAA[A/G]TATGTAATAGCTTTT	4297
rs138741491	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, downstream-variant-500B, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118527215	AGCTGGAGAACACCT[C/T]CTCTAGCTGCACTCC	4297
rs138785863	snp	A/C	3.29516e-05	0.00405891	missense	KMT2A	GRCh38.p7	11:118503699	GACAGAAACCTAATG[A/C]TTCCAGATGGCCCCA	4297
rs138800855	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118468580	ACACAGCTCCTATTT[A/G]TCTGTAATAAAGCTG	4297
rs138846300	snp	G/T	0.00636936	0.0560724	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520594	AGGCGGAGGTTACAG[G/T]GAGCCGAGATCGCAC	4297
rs138868861	snp	A/G	0.000214849	0.0103624	synonymous-codon	KMT2A	GRCh38.p7	11:118504106	CACAGCCACAACAAG[A/G]AAAAGCAGCCAGATT	4297
rs138874232	snp	C/T	3.36361e-05	0.00410084	synonymous-codon	KMT2A	GRCh38.p7	11:118482046	AGAAGTTCCCAAAAC[C/T]ACTCCTAGTGAGCCC	4297
rs138913980	snp	C/T	3.2956e-05	0.00405918	missense	KMT2A	GRCh38.p7	11:118503322	TGACTCCTGAGTATA[C/T]GGGCCAACGACCATG	4297
rs138922408	snp	C/T	0.0501905	0.150254	intron-variant	KMT2A	GRCh38.p7	11:118485996	GCTGAGGCAGGAGAA[C/T]GGCATGAACCCGGGA	4297
rs138969270	snp	C/T	0.000214435	0.0103524	missense	KMT2A	GRCh38.p7	11:118505292	GGAGGTGGTCTCACC[C/T]TTACCACAGGACTAA	4297
rs139001366	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118444866	AAATGTGAGGCACTG[C/T]ACCCAACCAGAAAAG	4297
rs139108099	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118480597	TGTGTCACATTTCTA[C/T]GCTTCTATTTTTTAA	4297
rs139119128	snp	G/T	3.32973e-05	0.00408014	missense	KMT2A	GRCh38.p7	11:118509164	CTTCCGGAAGTTCAG[G/T]TGACCCAAAATCCAG	4297
rs139123379	snp	C/T	1.64779e-05	0.00287031	missense	KMT2A	GRCh38.p7	11:118491306	AAATGTGAGAATCTT[C/T]CAGGTACAGAAGGTT	4297
rs139132855	snp	C/T	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118486933	AAAATCCAAGCTAGG[C/T]TGAAATCTGAATGTT	4297
rs139133297	snp	C/T			intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118518909	GGTGAAACTCCGTCT[C/T]TACTAAAAATACGAA	4297
rs139176242	snp	A/G	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118489264	AAAACTATATGGGAG[A/G]ATGTGCATTTTGTTA	4297
rs139222320	snp	C/G	0.0119091	0.0762411	intron-variant	KMT2A	GRCh38.p7	11:118476270	AAGAAATAGTTTTTG[C/G]TTAGATAAGCCGTAT	4297
rs139227835	snp	A/G/T	0.00125127	0.0249816	missense, intron-variant	KMT2A	GRCh38.p7	11:118473885	CTTTGTATCCTGTGG[A/G/T]TAGGGTTTCCAAAGA	4297
rs139242749	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118454256	CAGATTCCTTACTAT[A/G]GCCAACAAAGCCACA	4297
rs139318089	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118461390	TCACTTAGGAAGTGA[C/T]ATTACATAGCTTAAT	4297
rs139366882	snp	A/G	0.000153988	0.00877328	missense	KMT2A	GRCh38.p7	11:118506243	TCTGGGGAAGCAGAC[A/G]AACACTATCAGCTTC	4297
rs139375279	snp	G/T	0.00358779	0.0422022	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118523426	ATGACACTACTGCCC[G/T]GATTACTCCTTAGGA	4297
rs139441048	in-del	-/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118513959	AAAAAAAAAAAAAAA[-/G]AAAAAGAAAAAAAAG	4297
rs139450035	snp	C/T	1.64781e-05	0.00287033	missense	KMT2A	GRCh38.p7	11:118502629	CAAGTGCCAAAGTAG[C/T]TGATCATGTCTTAGG	4297
rs139469741	snp	A/G	4.94246e-05	0.0049709	synonymous-codon	KMT2A	GRCh38.p7	11:118504589	GGGTCTTTTTGAAGT[A/G]TTTTCTCAGCAGCTG	4297
rs139485216	snp	A/G	0.00199481	0.0315187	intron-variant	KMT2A	GRCh38.p7	11:118477451	TTAGATTAGACTTTT[A/G]TTTTCAGTATTTGGA	4297
rs139632016	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118500410	AAATTCCCCTTCTAC[C/T]ACTCCCGCGTTGGAG	4297
rs139787324	snp	A/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118443283	GAAATACAGAGACAC[A/T]TGGACTGAGGGAATG	4297
rs139922222	snp	A/G	0.00318978	0.0398085	intron-variant	KMT2A	GRCh38.p7	11:118469659	ATGCATTCCCCATCT[A/G]TGCTGCCATTCTGAC	4297
rs139936114	snp	C/T	0.00398564	0.0444627	intron-variant	KMT2A	GRCh38.p7	11:118483050	CCAGCCTGGCCAACA[C/T]GGTGAAACCCTGTCT	4297
rs139989306	snp	C/T	0.00179396	0.0298958	missense, intron-variant	KMT2A	GRCh38.p7	11:118474124	GAGAAGGAGAAAACC[C/T]TCTGCCTTTCCACTC	4297
rs140033934	snp	C/T	1.64741e-05	0.00286998	synonymous-codon	KMT2A	GRCh38.p7	11:118488670	TTGTTTAGAGGAGAA[C/T]GAGCGCCCTCTGGAG	4297
rs140049161	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118460747	TAATAGGGGACCACA[A/G]CCTTGAACTCCTGGT	4297
rs140088873	snp	C/T	0.00159617	0.0282053	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118515364	TTCTTCCTGTGCCTA[C/T]GGAAATCCCAACTCT	4297
rs140149257	snp	G/T	0.00438332	0.0466095	intron-variant	KMT2A	GRCh38.p7	11:118476568	ACTCCTGGCCTCAAA[G/T]GATCTTCCCACCTCA	4297
rs140150911	in-del	-/AAAAACC			frameshift-variant	KMT2A	GRCh38.p7	11:118495777	GGAGCGAGAGGAAAA[-/AAAAACC]CAGCCACACTGAGCA	4297
rs140200473	snp	C/T	0.00121897	0.0246576	missense	KMT2A	GRCh38.p7	11:118506166	CTGCTGCAATAACAG[C/T]GGCATCTAGCATCTG	4297
rs140215902	snp	A/T	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118470550	GTTGTAATTAGGATA[A/T]GTTGAGAAAGGAGCT	4297
rs140221671	snp	C/G	1.64972e-05	0.00287199	missense, intron-variant	KMT2A	GRCh38.p7	11:118472749	TAGGAGAAGCAGAAG[C/G]TATTCAGTGTCGGAG	4297
rs140355505	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118474629	GAATGAACTAAGGTT[A/G]GGACTATATCACAGA	4297
rs140439290	snp	C/T	0.000164802	0.00907599	synonymous-codon	KMT2A	GRCh38.p7	11:118493083	TCCAGACTTAAATCC[C/T]GAGACAGAGGAGAGT	4297
rs140442678	snp	C/T	0.000153988	0.00877328	synonymous-codon	KMT2A	GRCh38.p7	11:118503356	CAATGTTTCTTCTGA[C/T]AAGATTGGTGATAAA	4297
rs140472609	snp	A/G	0.00636936	0.0560724	intron-variant	KMT2A	GRCh38.p7	11:118443546	GATATAAATCCCCTT[A/G]AAGGATTAGTCCAAA	4297
rs140529566	snp	A/G	4.94311e-05	0.00497123	missense	KMT2A	GRCh38.p7	11:118502524	AGCGGTCCAAACTCC[A/G]GATAATGTCTCCAAT	4297
rs140545520	snp	A/G	1.64754e-05	0.00287009	missense	KMT2A	GRCh38.p7	11:118498047	CTAAAGAATGTGCAT[A/G]TGGCTGTGATCAGGG	4297
rs140548273	snp	C/T	0.00398564	0.0444627	intron-variant	KMT2A	GRCh38.p7	11:118441535	GTGAATTCCAGACTA[C/T]CCAAAAGAGAAGTTA	4297
rs140579592	snp	A/C	0.00398564	0.0444627	intron-variant	KMT2A	GRCh38.p7	11:118451365	CATAGGCTCACAACA[A/C]CATGCCTACTAATTT	4297
rs140633990	snp	A/T	0.0490535	0.14873	intron-variant	KMT2A	GRCh38.p7	11:118495168	TTTATTTATTTATTT[A/T]TTTTTTTTTGAGACG	4297
rs140726591	snp	C/T	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118445027	CCCTAATTGTTAGAA[C/T]CAAGAGATTGAAAGG	4297
rs140786729	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118464309	CAGAGGCCAAGGTGG[A/G]TGGATCACCTGAGGT	4297
rs140845031	snp	A/G	1.64751e-05	0.00287007	missense, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521395	TCCAGACTGACAAGC[A/G]GGAAAAGTATTACGA	4297
rs140845386	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118526606	AAAAAAAAGGAAAAT[A/G]TGTCTAAAGTCCATC	4297
rs140941483	snp	C/G/T	6.59287e-05	0.00574113	missense	KMT2A	GRCh38.p7	11:118505235	TCTGTTAGTTCTACA[C/G/T]CCAGTGTGATGGAGA	4297
rs140950788	snp	C/G	0.00874735	0.0655527	intron-variant	KMT2A	GRCh38.p7	11:118479086	AAGCATTTATCCTTT[C/G]TATTACAAACAATCC	4297
rs141004205	snp	A/G	4.95511e-05	0.00497726	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118472416	CAGTGCTATCTCCTC[A/G]CGGATCATTAAGACC	4297
rs141036837	snp	C/T	0.00199481	0.0315187	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118524167	AGAACCCATTGATCA[C/T]CTTGTGCCCTCTTTT	4297
rs141105330	in-del	-/C	0.0174175	0.0916809	intron-variant	KMT2A	GRCh38.p7	11:118460437	GACCACAGGCATGCA[-/C]CAGCACACCCAGCTA	4297
rs141108621	snp	C/T	0.0146672	0.084371	intron-variant	KMT2A	GRCh38.p7	11:118478496	CATGTGGCTATTGAG[C/T]GCTTGACATGTGATT	4297
rs141123090	snp	A/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118475355	TTAGGGTTTTAAAAA[A/T]ATCGTCATGTAGTAG	4297
rs141131964	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118481315	AGTTCAATTGTTTTA[A/C]TTTTTAGCTCCCACA	4297
rs141164463	snp	A/C	0.00755907	0.0610114	intron-variant	KMT2A	GRCh38.p7	11:118462993	CTGACAGCTCAGTGG[A/C]ACTCTTGTTTTGGAA	4297
rs141178238	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118509861	ATGTTGTTAGGCTTA[A/G]AGATCATTTATGTAA	4297
rs141200318	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118497875	TGGAAAAGCTAATGC[C/T]GAGGAAAACCTCCTT	4297
rs141368691	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118443857	GCTGGAGTTTCTTCC[A/G]TATATAGTGTTTTAT	4297
rs141407877	snp	A/T	6.59217e-05	0.00574078	missense	KMT2A	GRCh38.p7	11:118506544	TTCAGCTGCCTCTAG[A/T]CAAAGGGAATGGCAA	4297
rs141426962	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118500632	TTTTATTTTCAGGCC[A/G]TACTTTGTATACATT	4297
rs141438728	snp	A/G	0.00676609	0.0577691	intron-variant	KMT2A	GRCh38.p7	11:118497061	CCAGGCTGGAGTGCA[A/G]TGGCGTGATCTCGGC	4297
rs141454478	snp	C/T	1.64936e-05	0.00287168	missense, intron-variant	KMT2A	GRCh38.p7	11:118473546	CCTTAAACCCAACTT[C/T]TACTTTTCCTTCTCA	4297
rs141471060	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520679	GGGCGCTCATTTTAT[A/G]AGGCACTCGTTCAGT	4297
rs141515578	snp	C/G	3.34448e-05	0.00408917	splice-donor-variant	KMT2A	GRCh38.p7	11:118507610	TGGGCAACCTGCAGG[C/G]TAAGCTGAAGAATTC	4297
rs141562970	snp	C/T	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118437233	CCGGGGTTTCCCATC[C/T]CGGGACTGAACCCCT	4297
rs141579106	snp	A/T	6.59011e-05	0.00573988	synonymous-codon	KMT2A	GRCh38.p7	11:118505978	TAGTGCGTCAGTTCC[A/T]GGACACGTCACCTTA	4297
rs141580563	snp	A/G	0.000701445	0.0187144	intron-variant	KMT2A	GRCh38.p7	11:118490281	GTTTTGCCAGCTTTC[A/G]GAGGTTGTACTTGGT	4297
rs141644096	snp	C/T	0.00141865	0.0265954	intron-variant	KMT2A	GRCh38.p7	11:118484837	AATTGTAAAACTTTC[C/T]TAAGTGACCTTTCTC	4297
rs141727765	snp	A/G	0.0016869	0.0289932	KMT2A	11	allele_origin=G(germline)/A(germline)	11:118502464	TCTCCTCTGGACTTC[A/G]AAGCATTGGCTCCAG	4297
rs141735508	snp	C/T	3.30568e-05	0.00406538	synonymous-codon	KMT2A	GRCh38.p7	11:118507559	GGCTGAGCAGCAGGA[C/T]ACAGCTAGCGTGGAG	4297
rs141783388	snp	G/T	0.00199481	0.0315187	intron-variant	KMT2A	GRCh38.p7	11:118453447	TTTCTTCTTAACTCA[G/T]TGGCTGTTAATTTTC	4297
rs141789464	snp	C/T	0.00279162	0.0372561	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118513483	GCACTTTAGAAAATA[C/T]TAACATTTGTTCATT	4297
rs141812809	snp	A/C	1.64749e-05	0.00287005	missense	KMT2A	GRCh38.p7	11:118488692	CCTCTGGAGGACCAG[A/C]TGGAAAATTGGTGTT	4297
rs141890464	in-del	-/GAA			intron-variant	KMT2A	GRCh38.p7	11:118482776	AAAAAAGAAGAAGAA[-/GAA]GAAGTTAGCCAGGCA	4297
rs141892675	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118469189	ATCTATCAGGCCACA[C/T]TGGGTTTATTCTTTC	4297
rs141926731	snp	C/T	0.00597247	0.0543191	intron-variant	KMT2A	GRCh38.p7	11:118469083	GCCATGCTGGTGCGC[C/T]GCACCCACTAACTCG	4297
rs141959511	snp	A/G	0.000153988	0.00877328	missense	KMT2A	GRCh38.p7	11:118478008	GATGCTGAACCTCTT[A/G]CTCCACCCATCAAAC	4297
rs141961986	snp	C/T	0.000777637	0.0197031	synonymous-codon	KMT2A	GRCh38.p7	11:118484969	TGCCAGTAGTGGGCA[C/T]GTAGAGGTAAGGCAT	4297
rs141971802	snp	A/G	4.94409e-05	0.00497172	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473025	TAGGTGGACTTCTTT[A/G]AAGCATTCTAGGTCA	4297
rs141987822	snp	C/T	0.0170251	0.090679	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118516906	TTTTCCCATTATCAA[C/T]ACAATATTAATCTCA	4297
rs142024724	snp	A/G	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118461141	TTAGGGTTCACTTAG[A/G]TTCTTTTGTGGGAGA	4297
rs142052731	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118511774	GAGTGTACCTTTTCG[G/T]CTCCTTTCACATGTA	4297
rs142138730	snp	C/T			missense, intron-variant	KMT2A	GRCh38.p7	11:118472438	ATTAAGACCCCTCGG[C/T]GGTTTATAGAGGATG	4297
rs142212840	snp	C/T	3.3295e-05	0.00408	missense	KMT2A	GRCh38.p7	11:118509168	CGGAAGTTCAGGTGA[C/T]CCAAAATCCAGCAAA	4297
rs142250584	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118485247	ATGTCTAAATAAGAG[-/A]AAAAATTATACAGTG	4297
rs142254191	snp	A/G	0.00478085	0.0486577	intron-variant	KMT2A	GRCh38.p7	11:118443290	AGAGACACTTGGACT[A/G]AGGGAATGACTTCCC	4297
rs142282801	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118469467	AGGCTGTATTAAAAT[-/A]AAAAAATGGAAAATT	4297
rs142319007	snp	A/C	0.00557542	0.0525036	intron-variant	KMT2A	GRCh38.p7	11:118500248	TGGATAAAACAGCTC[A/C]TGCCCTGTTCCCAAC	4297
rs142437794	snp	A/G	0.00478085	0.0486577	intron-variant	KMT2A	GRCh38.p7	11:118487261	TCCTTCAACTTCTGG[A/G]ATTAAACAGATTTTT	4297
rs142445651	snp	A/G	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118508752	AGGTGAAAATTGATT[A/G]TGGTTTATAAGCTCA	4297
rs142499035	snp	C/T	0.000412048	0.0143476	synonymous-codon	KMT2A	GRCh38.p7	11:118504349	CACAAGTACCCCCTC[C/T]GACAAAAATTTACTG	4297
rs142543449	snp	A/G	1.64887e-05	0.00287125	missense	KMT2A	GRCh38.p7	11:118476826	GAAAGTGACTCATCA[A/G]AGACCTCTGTGCGAG	4297
rs142585619	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118526236	GGATTTTTTTCTGCC[C/T]ATGAATGTTGCCAGT	4297
rs142658261	snp	C/G	8.25539e-05	0.00642418	missense	KMT2A	GRCh38.p7	11:118481802	ACGTGGTGGACTCTA[C/G]TCAGAAACCTACCCC	4297
rs142756056	snp	A/C	0.0123036	0.0774623	intron-variant	KMT2A	GRCh38.p7	11:118453095	ATATAAAACTATCTG[A/C]CTTAATATAATCCTT	4297
rs142789239	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512333	AAATCTACTTTCTGT[C/G]TCTATGTATTTGATT	4297
rs142790228	snp	A/G	0.00358779	0.0422022	intron-variant	KMT2A	GRCh38.p7	11:118446293	GGCAGAGGTTGCAGT[A/G]AGCTGAGATCACACC	4297
rs142796581	snp	A/G	0.000153988	0.00877328	missense	KMT2A	GRCh38.p7	11:118505457	CCTTCAGGCCTGCTT[A/G]TTGGGGTTCAGCCTC	4297
rs142807735	snp	C/G	0.000181268	0.00951847	missense	KMT2A	GRCh38.p7	11:118503875	GAAGAAGCGAGGCAA[C/G]AGATCAGCTGAAGGA	4297
rs142830885	snp	G/T	0.000280424	0.0118378	synonymous-codon	KMT2A	GRCh38.p7	11:118499836	CTTTCCTTGGTCAGG[G/T]TCTATGACAATCGAC	4297
rs142864236	snp	C/T	0.0103295	0.0711199	intron-variant	KMT2A	GRCh38.p7	11:118449782	TCTTACTCCCATTAC[C/T]ATTGGTCATTCAACA	4297
rs142875797	snp	A/T	0.00143244	0.0267239	synonymous-codon	KMT2A	GRCh38.p7	11:118504931	TAGCCCTCCTTGTGG[A/T]TCAGTAGAGCAAGGT	4297
rs142941582	snp	A/G/T	0.00225106	0.0334733	intron-variant	KMT2A	GRCh38.p7	11:118499264	AGTATAATGTGCAAA[A/G/T]GGACAGCCTATTAAC	4297
rs142948344	snp	G/T	0.00247586	0.035097	synonymous-codon, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520877	TAAGGAGGCAGTTGG[G/T]GTCTACAGGTATGAC	4297
rs142963699	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118456038	TTAGACAAGTCATCT[C/T]CCTTTGTTGCCCAGG	4297
rs142985138	snp	C/T	0.000874263	0.0208894	missense	KMT2A	GRCh38.p7	11:118503075	CAATCAGCAAACTCC[C/T]CTCCAGATGAAGATA	4297
rs143060040	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118435396	AGAGCTCGCCGCCGG[C/T]GGGCCCCTTCCACCC	4297
rs143123487	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118480724	CTGGGGTGCAGTAGC[A/G]TGATTATGACTCACT	4297
rs143144585	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118459843	AGGCGGGCACTACCA[C/T]GCCCGGCTAATTTTT	4297
rs143178739	in-del	-/GGGGG			intron-variant	KMT2A	GRCh38.p7	11:118496878	TACCTCAGAGTGGCT[-/GGGGG]GTGAGGATTAAATGA	4297
rs143183708	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118476409	TAAGATAGGGTCTCA[C/T]TCTGTCACCCAGGGT	4297
rs143205627	snp	A/T	0.0023933	0.0345097	intron-variant	KMT2A	GRCh38.p7	11:118478828	TGACATGATCATAGC[A/T]CACTGCCAACACTGA	4297
rs143218182	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118484689	CTAGGTGAGCCTTTT[A/C]ATAGTCCGTGTCTGA	4297
rs143317202	snp	A/G	0.000214131	0.010345	missense	KMT2A	GRCh38.p7	11:118491813	TGAACTGTACTGAGC[A/G]GCACCCTGCAGAGTG	4297
rs143349186	snp	A/G	3.30246e-05	0.0040634	missense	KMT2A	GRCh38.p7	11:118474233	ACAAGAGGGTTGCCA[A/G]CCTCCTAAAAAAGGC	4297
rs143373748	snp	A/G	0.000153988	0.00877328	missense	KMT2A	GRCh38.p7	11:118497955	CTGGTCGTTTACTAT[A/G]TATTGGCCAAAATGA	4297
rs143420861	snp	A/G	1.65457e-05	0.00287621	missense, intron-variant	KMT2A	GRCh38.p7	11:118472649	CTTCTGAGGAGATTC[A/G]GGTACTTCCTGAGGA	4297
rs143424644	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118445206	TAAACTAGGTGGAAC[C/T]AAATTGAAGGCCAGC	4297
rs143525945	snp	A/C/G	0.000115329	0.00759291	missense	KMT2A	GRCh38.p7	11:118503400	CAGGAGTCCCCAAAG[A/C/G]TCCACCCATGCAAGT	4297
rs143558196	snp	A/G	0.00159617	0.0282053	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512431	AACAGAATACTTTCC[A/G]GGTTCTTCCCTTCTG	4297
rs143699272	snp	C/T	0.0123036	0.0774623	intron-variant	KMT2A	GRCh38.p7	11:118455224	TTTGTTATATGTTTA[C/T]TTTCTGTCTCTCCAT	4297
rs143706780	snp	C/T	1.6528e-05	0.00287467	synonymous-codon	KMT2A	GRCh38.p7	11:118482471	CCGCCCAAGTATCCC[C/T]GTAAAACAAAAACCA	4297
rs143721596	snp	C/T	0.00024707	0.0111119	synonymous-codon	KMT2A	GRCh38.p7	11:118505057	GCCCAATTCTACTGA[C/T]AGTCCTGGCCCGTCT	4297
rs143740430	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118434731	AACAACGGAATCTTG[C/T]TCTGTGTATTGCGTT	4297
rs143766206	snp	C/T	0.00199481	0.0315187	intron-variant	KMT2A	GRCh38.p7	11:118451167	ACTGGGGCTCTACCA[C/T]TGGAGACGTCCCTTC	4297
rs143780031	snp	A/C	1.64795e-05	0.00287045	missense	KMT2A	GRCh38.p7	11:118506189	AGCATCTGTGTGCTC[A/C]CCTCCACTCAGACTA	4297
rs143843795	snp	A/G	0.000790722	0.019868	missense	KMT2A	GRCh38.p7	11:118504857	GTAGATCCAACTCCT[A/G]AAGGCCACATGACTC	4297
rs143955975	snp	A/G	1.64738e-05	0.00286995	missense	KMT2A	GRCh38.p7	11:118505838	GGAACTGCTGCCACA[A/G]CGGCAGGCACATCAA	4297
rs143985343	snp	C/T	1.64933e-05	0.00287165	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473421	ATCTCCTTCTCACTC[C/T]ATGAGGACAAGAAGT	4297
rs143998546	snp	A/C	3.31257e-05	0.00406962	missense, intron-variant	KMT2A	GRCh38.p7	11:118471844	AGACCTCCCACCTTC[A/C]CTGGAGTAAAAATCA	4297
rs144034334	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118441211	GTCTCACTATGTTGC[C/G]CAGGTGCATCTTGAA	4297
rs144067538	snp	A/C/T	0.000110578	0.0074349	intron-variant	KMT2A	GRCh38.p7	11:118481675	TTAAATAAAATTATT[A/C/T]TCACTATAGACAGAT	4297
rs144075635	snp	A/G	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118478301	AGGAAACTGAATGTG[A/G]TTGTAATTGAGTTGC	4297
rs144127791	snp	A/G	0.000115774	0.00760748	missense, intron-variant	KMT2A	GRCh38.p7	11:118472352	AGCTGCAGGGAAGAA[A/G]GGTGAAGACACAGGT	4297
rs144157557	snp	C/T	0.0146672	0.084371	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118524223	CAGTCTGACCACTCA[C/T]GATAAAGCAGATTTT	4297
rs144180211	snp	C/T	1.66355e-05	0.002884	missense	KMT2A	GRCh38.p7	11:118495861	AACCAGACTCACCAA[C/T]TCCTCTGCATCCTCC	4297
rs144222529	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118516998	GTGAAAATATACTTG[A/G]GTATGTAGTATGTTT	4297
rs144228979	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118499571	GGCAGATCACTGGAG[A/G]TTCAGGAGTTGGAGA	4297
rs144235455	snp	A/G	3.2963e-05	0.00405961	missense, intron-variant	KMT2A	GRCh38.p7	11:118473984	CATCACATGATTCTG[A/G]GACTGATATTACTTC	4297
rs144271443	snp	C/T	0.00107034	0.0231089	missense	KMT2A	GRCh38.p7	11:118502590	CCTCAGTCTCCACCA[C/T]CGGGACCGCTACTGA	4297
rs144359798	snp	A/G	0.00438332	0.0466095	intron-variant	KMT2A	GRCh38.p7	11:118500417	CCTTCTACCACTCCC[A/G]CGTTGGAGTCTCATT	4297
rs144409818	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118481059	GTACATGGGATGTCC[A/C]TTACCTCAAGCATTT	4297
rs144499971	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118441695	CTGAAATGGTTTATA[C/G]TGAGCATTAGAAATT	4297
rs144567514	snp	C/G	0.00279162	0.0372561	intron-variant	KMT2A	GRCh38.p7	11:118497430	AGACCAGGTCTTGCT[C/G]TGTCACCCAGACTAG	4297
rs144608351	snp	A/G	0.000153988	0.00877328	missense	KMT2A	GRCh38.p7	11:118501791	ATCTCAAAGGTCCCC[A/G]GGATTCGAACACCCA	4297
rs144675903	snp	A/G	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118447193	AAAAAATTTAACCCC[A/G]TATACCTTATGTCGT	4297
rs144687085	snp	C/T	0.00398564	0.0444627	intron-variant	KMT2A	GRCh38.p7	11:118469139	AATGCTATCCCTCCC[C/T]CCTCCCCCCAGCTAG	4297
rs144694397	snp	C/T	8.41885e-05	0.00648746	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118471969	GCAAGCCACAAAGAT[C/T]AAAAAATTAAGAGCA	4297
rs144742133	snp	G/T	1.64741e-05	0.00286998	synonymous-codon, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521986	CTTCATCAATCACTC[G/T]TGTGAGCCTAACTGC	4297
rs144791689	snp	C/T	0.00835141	0.0640778	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118515610	CAGTGTTCAGAGGAA[C/T]AGGAGAGGCTTAGGA	4297
rs144802429	snp	A/C	0.00119737	0.0244387	upstream-variant-2KB, downstream-variant-500B, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118527093	GACAAAGGAACAGGG[A/C]CTTTACCTTCTACAT	4297
rs144844866	snp	A/G	9.89413e-05	0.00703284	missense	KMT2A	GRCh38.p7	11:118510053	CTGAGAAAAAACCCA[A/G]GAAAGGACTTGTTTT	4297
rs144899568	snp	C/G	0.00795532	0.062565	intron-variant	KMT2A	GRCh38.p7	11:118470837	TTTAGAAACAGTCTT[C/G]TTTTCTTGAATGGCT	4297
rs144908612	snp	A/C	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118469976	AAGTCTTAAAACTTC[A/C]TATAGGAAAGGAATT	4297
rs144944070	snp	A/G	8.23689e-05	0.00641698	synonymous-codon	KMT2A	GRCh38.p7	11:118491826	GCGGCACCCTGCAGA[A/G]TGGCGACTGGCCCTT	4297
rs144970503	snp	C/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118462825	CGTCGGCCTCCTAAA[C/G]TCCTGGGATTACAGG	4297
rs144994538	in-del	-/C			intron-variant	KMT2A	GRCh38.p7	11:118454997	GCTAACACCTCTCCA[-/C]CCCCCACTCCTGTCA	4297
rs145028869	snp	A/G	4.962e-05	0.00498072	missense	KMT2A	GRCh38.p7	11:118503199	AAGGGAAAAAATCCT[A/G]TAAAGAAACTTTCAA	4297
rs145061625	snp	C/T	0.000164967	0.00908056	missense	KMT2A	GRCh38.p7	11:118501013	TATACTGGAGCACCA[C/T]AGATGCTCGCAAGCG	4297
rs145151822	snp	A/C	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118444700	TGTCTCAGCCTCCTA[A/C]GTAGCTGGGACTACA	4297
rs145186221	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118435434	CATAATGCCCAACGC[C/T]CTCCTCCTCCCCCTC	4297
rs145193113	in-del	-/C	0.0865458	0.189163	intron-variant	KMT2A	GRCh38.p7	11:118437676	ATACAGCAGTCTCTT[-/C]CCCCCCCCGCCCCGT	4297
rs145249825	snp	C/T	0.000428223	0.0146263	missense	KMT2A	GRCh38.p7	11:118506367	CCCAGACGGTAGACG[C/T]TCCTAATAGCATGGG	4297
rs145288366	snp	C/T	0.00517822	0.0506191	intron-variant	KMT2A	GRCh38.p7	11:118494949	AATTGCCTTTTTGTT[C/T]TTTACTTTTATATTT	4297
rs145323316	snp	A/C	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118489295	TATGCAAATGCTGCA[A/C]CATTTTGTCTAGGGA	4297
rs145356539	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118462103	GGACTACAGGCGCGT[A/G]CCACCATAACTGGAT	4297
rs145452548	snp	A/G	0.000481876	0.0155147	synonymous-codon	KMT2A	GRCh38.p7	11:118501844	CCCTGGCTGTCGACC[A/G]TTGCCTTCTGCAGGT	4297
rs145474318	snp	A/G	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118474830	TTTTTGCAGAATACA[A/G]ATGAGAAGTACTGGC	4297
rs145549283	snp	A/G	1.65457e-05	0.00287621	missense	KMT2A	GRCh38.p7	11:118476805	TTGCCTCATATTCAG[A/G]GTCAAGAAAGTGACT	4297
rs145604373	snp	A/G	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118483621	GCCCCACATGTTCTA[A/G]CCTAGGAATCTGCTT	4297
rs145665304	snp	A/G	0.00755907	0.0610114	intron-variant	KMT2A	GRCh38.p7	11:118477073	AGGCTCTTCATAGTT[A/G]GTAGGTCCTCTGAAA	4297
rs145722521	snp	A/G	0.00478085	0.0486577	intron-variant	KMT2A	GRCh38.p7	11:118457871	AGCATAGCAGGCAAC[A/G]TACGATACTTCATTA	4297
rs145789893	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118452076	CACTATGTTACCTGC[A/G]CTGGAGGGCAGTGGC	4297
rs145803732	snp	C/T	0.00279162	0.0372561	intron-variant	KMT2A	GRCh38.p7	11:118495568	TCAGCAATTTTCAAA[C/T]GCTGTGACTTGTTCT	4297
rs145811623	snp	A/T	0.000153988	0.00877328	missense	KMT2A	GRCh38.p7	11:118480221	CTTCCAAAGCCTACC[A/T]GCAGAAGCAAGCTAA	4297
rs145816717	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118496736	TAGGATAGCAGAATC[A/G]TTAAGAGCCCGAGTT	4297
rs145857563	snp	A/G	1.65247e-05	0.00287438	synonymous-codon	KMT2A	GRCh38.p7	11:118502699	CACCTCTTCAAATTT[A/G]CAAAGGACAGTGGTT	4297
rs145912719	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118492754	TTATCTTTTAATAGA[C/G]CTCCATTTTTTGAAT	4297
rs145943534	snp	C/T	0.00370147	0.0428606	synonymous-codon	KMT2A	GRCh38.p7	11:118503932	CACTTCAGATGAAGA[C/T]GACTTATACTATTAC	4297
rs145944977	snp	A/G	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118493741	TTGAGATGGAGTCTC[A/G]CTCTGTTACCCAGGC	4297
rs145977255	snp	C/T	0.0023933	0.0345097	intron-variant	KMT2A	GRCh38.p7	11:118487396	ACTCCTAAAGCATGA[C/T]CAGTGCTTGATAAAC	4297
rs146028064	snp	A/G	0.000197668	0.00993955	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118474102	CGGCCCAACTGCCCC[A/G]TCCCTGGAGAAGGAG	4297
rs146046070	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118460604	CTTCAAGAGTTAAGC[A/G]AAATTTTTTATTCCA	4297
rs146062129	in-del	-/T			frameshift-variant, intron-variant	KMT2A	GRCh38.p7	11:118472245	GTTAGGATTATTCCT[-/T]TCTTCAAAAAGGACA	4297
rs146065015	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118454894	ATGGTGGGCCAAATT[C/T]GGCCTGTGGCCCATA	4297
rs146069428	snp	C/G/T	0.000181377	0.00952144	synonymous-codon, missense	KMT2A	GRCh38.p7	11:118505265	ACAAATACTTCAGTA[C/G/T]TGGGACCCATGGGAG	4297
rs146099945	snp	A/G	0.0271762	0.113356	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118514789	CAGGCATGTGCCACC[A/G]TGCCTGGCTAATTTT	4297
rs146181710	snp	C/T	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118486554	GCTTATTACTTACCA[C/T]ATAAGATATGTATTC	4297
rs146185599	snp	C/G	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118481647	GATCATATGGTGGCT[C/G]TGTAATTCTATTTTA	4297
rs146191865	snp	C/T	0.00135055	0.0259509	missense	KMT2A	GRCh38.p7	11:118509150	GGCAAGTCGCTGTTC[C/T]TCCGGAAGTTCAGGT	4297
rs146340723	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118461169	AGAAATATTCCTATT[A/G]CTTCGTCACTCACAG	4297
rs146343645	snp	G/T			missense, intron-variant	KMT2A	GRCh38.p7	11:118472278	TGCAACCATTGCTAA[G/T]CAACTCTTACAGAGG	4297
rs146434158	snp	C/T	0.000153988	0.00877328	missense	KMT2A	GRCh38.p7	11:118506463	CATCCTCTCCATCTT[C/T]TGGACAGCGGTCAGC	4297
rs146482645	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118482155	AAAAAGCACTGATGT[C/T]TCAAACAGCATTTGA	4297
rs146486605	snp	A/G	0.00398564	0.0444627	intron-variant	KMT2A	GRCh38.p7	11:118478352	TTTGTGGTGTGGGCT[A/G]TGCTTAAATAAGAAA	4297
rs146517864	snp	G/T	1.65222e-05	0.00287417	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118472398	GTTCATCATGCCTGT[G/T]GTCAGTGCTATCTCC	4297
rs146586576	snp	A/G	0.0115144	0.0749975	intron-variant	KMT2A	GRCh38.p7	11:118449981	ATAATAAAAAGAACT[A/G]TATCTGAAAATAAAG	4297
rs146605094	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118443620	TGAATGTATTGCCCT[A/G]ATGAGTTTTAGTTTT	4297
rs146608546	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118500419	TTCTACCACTCCCGC[A/G]TTGGAGTCTCATTTT	4297
rs146635751	snp	C/G	1.64792e-05	0.00287042	missense	KMT2A	GRCh38.p7	11:118504835	CCCAGCACTGCTGAG[C/G]CCAGGAGTAGATCCA	4297
rs146812027	snp	C/T	0.000153988	0.00877328	synonymous-codon	KMT2A	GRCh38.p7	11:118504913	GGATGCAGACCACAT[C/T]TCTAGCCCTCCTTGT	4297
rs146846144	snp	C/T	0.00755907	0.0610114	intron-variant	KMT2A	GRCh38.p7	11:118455362	ACAGTCATATTTGAA[C/T]TATGCCTGTAGCCTG	4297
rs146850350	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118451343	CAGCCTCCTGAGTAG[C/T]TGGGACCATAGGCTC	4297
rs146952018	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118463868	CATATCTGAACAGGA[G/T]GTAGTTTGAGGCACT	4297
rs146967399	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118458953	AGCCTTCAAAACAAA[A/G]TATTTCAAAAAACAA	4297
rs146970550	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118453216	TAATTGCTATTTCTA[C/T]TTTCTCACCTTTCAT	4297
rs147014136	snp	G/T	0.000813132	0.0201471	missense	KMT2A	GRCh38.p7	11:118506607	CTTCTGAAGCACACA[G/T]TCCAGACCAAGAAAC	4297
rs147072909	snp	A/T	0.00105423	0.0229347	synonymous-codon	KMT2A	GRCh38.p7	11:118484897	TGTGTGGGAGATGGG[A/T]GGCTTAGGAATCTTG	4297
rs147102502	snp	G/T	0.000198623	0.00996353	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473163	TGCATCTGGTTTTTC[G/T]GCATCTGGTACCGCT	4297
rs147197118	snp	C/T	0.00318978	0.0398085	intron-variant	KMT2A	GRCh38.p7	11:118499070	TGCTTTTTGAATTAT[C/T]TCGAAATGCAAAAGA	4297
rs147223140	snp	A/G	1.64751e-05	0.00287007	missense	KMT2A	GRCh38.p7	11:118503628	CCCAACCAAGCCCCA[A/G]TAATACCTCATGCCA	4297
rs147272445	snp	A/G	9.95702e-05	0.00705515	missense, intron-variant	KMT2A	GRCh38.p7	11:118471902	AGTTACCAAAGGGAA[A/G]CAAAGAAGATAGCCT	4297
rs147292591	in-del	-/AT			intron-variant	KMT2A	GRCh38.p7	11:118502304	TCCAGTTACCTATAA[-/AT]ATATATATATATAGT	4297
rs147308365	snp	A/G	1.64993e-05	0.00287218	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473478	ACCTCTCACCCCCCC[A/G]TCTTCTGTCTCTTCC	4297
rs147317561	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118523597	GTATATTTTTCTATG[A/G]GAAGCACTTCATAGG	4297
rs147408465	snp	A/G	0.00755907	0.0610114	intron-variant	KMT2A	GRCh38.p7	11:118446412	ACACCATCAGAAACC[A/G]TCAATACACCTCAGA	4297
rs147412214	snp	C/T	9.885e-05	0.0070296	missense	KMT2A	GRCh38.p7	11:118505476	GGGTTCAGCCTCCTC[C/T]GGATCCCCAACTTTT	4297
rs147438330	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118442082	TAATTAAGATCTCTT[C/T]GTGCCTGCCCACATT	4297
rs147515118	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118476488	GGTGTGTACCACCAC[A/G]CCCAGCCAATTTTTA	4297
rs147544070	snp	A/G	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118470328	TTTTGTTTTTGAGAC[A/G]GAGTCTCACTCTGTC	4297
rs147558153	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118516204	GTAAGTACCATGAAG[A/G]AGATAACATGGGGAA	4297
rs147574394	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118510632	CATTTTGTTTTGTCC[A/G]TGTTTGTTTACTTTT	4297
rs147615342	in-del	-/G			intron-variant	KMT2A	GRCh38.p7	11:118499289	TTAACAGCTACCATG[-/G]GGTTTTATTTAAGGT	4297
rs147741426	snp	A/G	1.70411e-05	0.00291895	synonymous-codon	KMT2A	GRCh38.p7	11:118481719	TTTTCCCTCAGCTGT[A/G]AAAAAGAAAGAGAAA	4297
rs147764171	snp	A/G	0.00136636	0.0261019	synonymous-codon	KMT2A	GRCh38.p7	11:118496334	CAATAGACAGTGTGC[A/G]TTATGTTTGACTTAT	4297
rs147768466	snp	A/G	0.0314385	0.121371	intron-variant	KMT2A	GRCh38.p7	11:118462831	CCTCCTAAAGTCCTG[A/G]GATTACAGGCGTGAG	4297
rs147771916	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118458639	CAAATGTGTGAACAC[A/G]TTTTTTAAAATTCCT	4297
rs147772025	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118524540	TGTCATCATGGAGAA[A/G]TGCCAGCAGGGGACT	4297
rs147788071	snp	C/T	0.00159617	0.0282053	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118517131	CTGGGCGCGGTGGCT[C/T]ACGCCTGTAATCCCA	4297
rs147844226	snp	A/C/G/T	9.88418e-05	0.00702946	missense	KMT2A	GRCh38.p7	11:118506472	CATCTTCTGGACAGC[A/C/G/T]GTCAGCAAGCCCTTC	4297
rs147874234	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118489948	CTATTGGACTTATGT[A/G]ACTTGTATTACAAAT	4297
rs147878170	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118484717	TGAGATTAAAACTTT[C/T]TAAAGCAGCAGTTAT	4297
rs147982461	snp	A/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118445296	AGAAGAAAGAGAACA[A/T]GATGGTAAATAGGCA	4297
rs148022594	snp	A/G	3.52075e-05	0.00419554	missense	KMT2A	GRCh38.p7	11:118506640	CATCCCTGACCTCAG[A/G]CACAGGGTGAGAGAT	4297
rs148049276	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512576	TTCTATTTTCTGCTA[C/T]GAATAATGTTGCCAC	4297
rs148077979	snp	C/T	1.6476e-05	0.00287014	synonymous-codon	KMT2A	GRCh38.p7	11:118505111	GACCACTCCACCCCA[C/T]CTGAAGCCAGCCACT	4297
rs148264553	snp	A/G	0.0107246	0.0724382	intron-variant	KMT2A	GRCh38.p7	11:118460133	ACATCTAGTTACTAT[A/G]GATAATTTAGGTCTT	4297
rs148319291	snp	C/G	0.000153988	0.00877328	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473493	GTCTTCTGTCTCTTC[C/G]TCGTTAAGCATTTCT	4297
rs148324206	in-del	-/GA	0.00716266	0.059414	intron-variant	KMT2A	GRCh38.p7	11:118509342	ATTTGGCCCACATTG[-/GA]GACTGAAACTTGGCG	4297
rs148437955	snp	C/T	0.000197964	0.00994701	synonymous-codon	KMT2A	GRCh38.p7	11:118504199	TGGGGAGAAAGAACA[C/T]GTCACTAAGAGTTCT	4297
rs148439270	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118490581	TTCAGTAGTTATATT[-/A]GAAAAAAATATTAAT	4297
rs148458977	snp	C/G	1.65211e-05	0.00287407	missense	KMT2A	GRCh38.p7	11:118476811	CATATTCAGGGTCAA[C/G]AAAGTGACTCATCAG	4297
rs148466234	snp	A/G	0.0115144	0.0749975	intron-variant	KMT2A	GRCh38.p7	11:118494894	TTGAAATGCCTTTTC[A/G]GTGTGGTTTTGAGGA	4297
rs148514018	snp	A/C/G	3.40136e-05	0.00412379	missense, intron-variant	KMT2A	GRCh38.p7	11:118472151	AGCCCCAGAAAGTCC[A/C/G]GAAAGACAAGGAAGG	4297
rs148519313	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118448278	TTGTCATTTAAAGAG[A/G]TATAGTTCAGAATAG	4297
rs148548051	snp	C/T	8.23703e-05	0.00641704	synonymous-codon, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519752	GCCAATGAACCCCCC[C/T]TGAACCCTCACGGCT	4297
rs148584651	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118516032	ATTCCCAGGATTGTC[A/T]TAGATTAATCATCTG	4297
rs148598896	snp	A/G	1.64732e-05	0.0028699	missense	KMT2A	GRCh38.p7	11:118505853	GCGGCAGGCACATCA[A/G]CAATAAGCCAGGATA	4297
rs148606323	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118481306	ATCTCCATAAGTTCA[A/G]TTGTTTTAATTTTTA	4297
rs148643334	snp	C/T	0.0663309	0.169604	intron-variant	KMT2A	GRCh38.p7	11:118487437	GCGAATTTTTTAAAC[C/T]TTTTATGTTGACATG	4297
rs148725584	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118499652	GGGAGTGGTGGTACA[A/T]CCCTATAATCCCAGC	4297
rs148958705	snp	A/C	0.000284131	0.0119157	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118434685	CTCCTGCTACTCCCA[A/C]CCTTTTAGCATCTAG	4297
rs149014176	snp	A/G	0.000115513	0.00759888	synonymous-codon	KMT2A	GRCh38.p7	11:118502849	GAGTTCCAAGAGCTC[A/G]GAGGGATCTGCACAT	4297
rs149040031	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118451985	TTCTTGAGTCAGTTG[A/T]CTTACACCAAATGTA	4297
rs149047036	snp	C/G	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118471156	CAGATTGAAATATGG[C/G]ACTCTGAGCTGCCCA	4297
rs149109658	snp	C/T	0.0532157	0.154195	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118518848	TTTGGAAGGCCAAGG[C/T]GGGTGGATCACGAGG	4297
rs149137886	snp	A/G	0.000642329	0.0179096	missense	KMT2A	GRCh38.p7	11:118506439	GCCCCACCTCTCCTG[A/G]GGGTTCTCCATCCTC	4297
rs149272864	snp	A/G	0.00199481	0.0315187	intron-variant	KMT2A	GRCh38.p7	11:118493991	GCTGGGATTACAGGC[A/G]TGAGCCACTGTTTAT	4297
rs149340870	snp	C/T	8.23703e-05	0.00641704	missense	KMT2A	GRCh38.p7	11:118505968	CCCCTACAAGTAGTG[C/T]GTCAGTTCCAGGACA	4297
rs149351885	snp	A/G	3.29658e-05	0.00405978	missense	KMT2A	GRCh38.p7	11:118501710	AACACAGCTGAAATT[A/G]TAAGTCCTCCATCAC	4297
rs149404438	snp	A/G	0.00189269	0.0307044	missense	KMT2A	GRCh38.p7	11:118482054	CCAAAACCACTCCTA[A/G]TGAGCCCAAGAAAAA	4297
rs149431696	snp	A/C	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118486395	TTTTTTTTAATCTTT[A/C]TGAGTTTTTTGCAGT	4297
rs149474220	snp	A/G	0.000153988	0.00877328	synonymous-codon	KMT2A	GRCh38.p7	11:118505765	CAACATCATAAAAAG[A/G]TCTAAATCTAGCATC	4297
rs149486532	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118438946	AGGCAGCTGCAGTCA[A/G]CAGGGTTGTTTGAGA	4297
rs149518043	snp	A/G	0.0228947	0.104514	intron-variant	KMT2A	GRCh38.p7	11:118459715	CCGTTGCCCAGGCTG[A/G]AGTACAGTGGCATGA	4297
rs149529128	snp	A/G	0.000153988	0.00877328	missense	KMT2A	GRCh38.p7	11:118503616	ATGGTCCAGTGGCCC[A/G]ACCAAGCCCCAATAA	4297
rs149555769	snp	C/T	0.00358779	0.0422022	intron-variant	KMT2A	GRCh38.p7	11:118454621	CCTGAAAAACCCATA[C/T]ATCAAAAATGTCATA	4297
rs149638083	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118480994	ATATATTTATGGGGG[C/T]ACATGAGATATGTTG	4297
rs149739040	snp	C/T	0.0146672	0.084371	intron-variant	KMT2A	GRCh38.p7	11:118483525	GTGACACCGAGACTC[C/T]GTCTCAAAAAAAAAT	4297
rs149767877	snp	A/G	0.000134587	0.00820216	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118471966	TCAGCAAGCCACAAA[A/G]ATTAAAAAATTAAGA	4297
rs149816147	snp	A/G	0.00279162	0.0372561	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118515434	AACAGAAAGTCCAGA[A/G]GTAGGGACAGACGTG	4297
rs149888768	snp	C/T	0.000153988	0.00877328	missense	KMT2A	GRCh38.p7	11:118502686	GGCAAAACACTTCCA[C/T]CTCTTCAAATTTGCA	4297
rs150022687	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118443582	TAAGAGGCCAAGCTT[G/T]GTTTAACTTTTAGAT	4297
rs150026749	snp	A/C	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118461396	AGGAAGTGACATTAC[A/C]TAGCTTAATTTGCTG	4297
rs150050498	snp	C/T	4.94629e-05	0.00497283	missense	KMT2A	GRCh38.p7	11:118504801	TCACAGAAAAATCTG[C/T]AGCCTCCTCTGAAAG	4297
rs150055331	snp	G/T	0.00398564	0.0444627	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118523503	ACAGAGTCCTGAACC[G/T]GTTAAATTAAGTCAT	4297
rs150112908	snp	C/T	0.000100015	0.00707089	missense	KMT2A	GRCh38.p7	11:118507606	AGTGTGGGCAACCTG[C/T]AGGGTAAGCTGAAGA	4297
rs150130005	snp	A/C	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118464375	ACCCCATCTCCACTA[A/C]AAATACAAAAATAAC	4297
rs150199390	snp	A/C	0.0115144	0.0749975	intron-variant	KMT2A	GRCh38.p7	11:118479220	TATTTTTTTGTACCC[A/C]TTAGCCATCCCCTAA	4297
rs150249045	snp	A/G	0.039522	0.134904	intron-variant	KMT2A	GRCh38.p7	11:118485811	CATATAGCTGGGCAC[A/G]GTGGCTCACGCCTGT	4297
rs150277124	snp	A/C/T	9.98443e-05	0.00706493	missense	KMT2A	GRCh38.p7	11:118482021	CACCTACTACAGGAC[A/C/T]GCCAAGAAAAGAAGT	4297
rs150282338	snp	C/T	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118500640	TCAGGCCGTACTTTG[C/T]ATACATTGTAAGGCA	4297
rs150286876	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118509860	AATGTTGTTAGGCTT[A/G]GAGATCATTTATGTA	4297
rs150328852	snp	A/G	0.000708104	0.0188029	missense, intron-variant	KMT2A	GRCh38.p7	11:118472969	GCTTCCACTGCTCCT[A/G]TGCAAGGGAAGCGAA	4297
rs150337256	snp	A/G	0.0209421	0.100162	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118517784	ATTCAAGGTTACAGT[A/G]AGCTATGATCATGCT	4297
rs150389677	snp	A/G	0.0267878	0.112589	intron-variant	KMT2A	GRCh38.p7	11:118475580	TCCAAAAAATTAGCC[A/G]GACATGGTGGCATGC	4297
rs150412512	snp	A/G	3.29522e-05	0.00405894	missense	KMT2A	GRCh38.p7	11:118503397	TGCCAGGAGTCCCCA[A/G]AGCTCCACCCATGCA	4297
rs150465296	snp	G/T	1.65869e-05	0.00287979	missense	KMT2A	GRCh38.p7	11:118498483	TGTCTTTCTGGATGA[G/T]AAAAAAGTATATTGC	4297
rs150493660	snp	C/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118451711	TTATGTAGCTGGTCT[C/G]GAACTCCCAGGCTCA	4297
rs150502030	snp	C/T	0.000362809	0.0134638	synonymous-codon	KMT2A	GRCh38.p7	11:118504524	TCTTCATCAGAACTC[C/T]TGAATCTTGGTGAAG	4297
rs150508721	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118477285	AGATTTGGCAAAGCT[A/G]TCCAGGAGTCTTTGA	4297
rs150545040	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118446218	GCTACATGTCGTGGT[A/G]CACACCTGCAATCCC	4297
rs150570074	snp	A/C/T	3.29567e-05	0.00405924	synonymous-codon, missense	KMT2A	GRCh38.p7	11:118502511	TCCTTATCACCCCAG[A/C/T]GGTCCAAACTCCGGA	4297
rs150598681	snp	A/G	0.00199481	0.0315187	intron-variant	KMT2A	GRCh38.p7	11:118453875	ATCTAAAAAGTCTTG[A/G]CTTTCTTCCTCAAAC	4297
rs150601976	in-del	-/G			intron-variant	KMT2A	GRCh38.p7	11:118438146	CTTTAGTGTGGTGGC[-/G]GGTGGTTGCTTTGGG	4297
rs150650414	in-del	-/G			intron-variant	KMT2A	GRCh38.p7	11:118438149	TAGTGTGGTGGCGGT[-/G]GGTTGCTTTGGGATG	4297
rs150665392	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118469316	AGATTTACACATTTT[A/G]TGTTATGTGGTAGTG	4297
rs150724970	snp	C/T	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118438296	GTACTGGGGCAAGAA[C/T]GGAGTTGCTTCTATA	4297
rs150774702	snp	A/G	0.00415482	0.0453888	intron-variant	KMT2A	GRCh38.p7	11:118488452	TCTCCCGCAGTGTCC[A/G]ATACTGTACTTTTTT	4297
rs150800017	snp	C/G	1.64939e-05	0.0028717	missense	KMT2A	GRCh38.p7	11:118489816	GAGTGTAATAAGTGC[C/G]GAAACAGCTATCACC	4297
rs150804738	snp	A/G	0.00488705	0.0491899	missense	KMT2A	GRCh38.p7	11:118505283	GGACCCATGGGAGGT[A/G]GTCTCACCCTTACCA	4297
rs150824395	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118513723	ATTGTTTGAGTCTAG[G/T]AGTTCAAGACCATCC	4297
rs151031938	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118479034	GGCATGCAATGCATC[A/C]TAATCATATCATGCA	4297
rs151037125	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118495245	CTCACTACAACCTCC[A/G]CCTCCCTGGTTCAAG	4297

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