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
rs151058616	snp	A/C	1.64738e-05	0.00286995	synonymous-codon, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521369	GTATGCCGGCAACGT[A/C]ATCCGCTCCATCCAG	4297
rs151144961	in-del	-/T			intron-variant	KMT2A	GRCh38.p7	11:118455671	CCCTTATTATTATTA[-/T]TTTTTTTTATTTTTA	4297
rs151193477	snp	A/C/T	9.92563e-05	0.0070441	missense, synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473358	TTCAGGAGTATCCAA[A/C/T]AGAAAAAGGAAAAGA	4297
rs151249834	snp	A/G	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118443499	ACATTTGAAAGAAGA[A/G]TTTTGTTACGTGATT	4297
rs151318976	snp	A/G	0.0064749	0.056529	intron-variant	KMT2A	GRCh38.p7	11:118509226	GGGTAAAAGGTTAGA[A/G]TCAGAGAATATCAAT	4297
rs151337923	snp	A/G	0.000197664	0.00993947	synonymous-codon	KMT2A	GRCh38.p7	11:118498004	TGCTTTGTGGTCAGC[A/G]GAAGTGTTTGAAGAT	4297
rs180809790	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118465636	CCTAAACCAACCCTT[C/T]TCTCCCCACATCCAG	4297
rs180828634	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118442569	AAGACAAGACAATCA[A/G]ATGAAATTATTGATT	4297
rs180830778	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118485150	TCTGCTATTAGAGTA[A/G]CAAAGTTATTGAGAG	4297
rs180966088	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118507777	CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT	4297
rs181059213	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118461150	ACTTAGGTTCTTTTG[C/T]GGGAGAAATATTCCT	4297
rs181076880	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118481397	TAACATAATGTCCTC[C/T]AGTTCCATCCATGTT	4297
rs181083745	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118443228	CTTTTGTTAGCCTTT[C/T]CATTTTGCCCCTCAA	4297
rs181116978	snp	C/T	0.00358779	0.0422022	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118513184	AGGAGTATGAGACTG[C/T]ATTAAGCTATGATCT	4297
rs181122034	snp	C/T	0.0146672	0.084371	intron-variant	KMT2A	GRCh38.p7	11:118485939	TACAAAAAAATTAGC[C/T]GGGTGTGGTGGCGGG	4297
rs181217887	snp	G/T	0.000183249	0.00957032	intron-variant	KMT2A	GRCh38.p7	11:118500956	TTCTATCCTCTCCCT[G/T]ATGATGATTTTCCCA	4297
rs181226207	snp	A/G			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118523647	GCTATTTTTTAAACC[A/G]CGGTATTATCCTAAT	4297
rs181248473	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118492665	GCCTGGGTGACAGAG[C/T]GAGAGTCCATCTCAA	4297
rs181338655	snp	C/T	0.00318978	0.0398085	intron-variant	KMT2A	GRCh38.p7	11:118461909	GAAGCCTGTTGCTCA[C/T]GATAGTGCAGTGAAA	4297
rs181350301	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118508628	CAGTCCAAGCTAAGG[C/T]GGGAGGATTGCTTGA	4297
rs181415065	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118438505	GGGCTGAAGCGAAGG[C/G]GGGTAGGGGGTTGCT	4297
rs181457789	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118482302	TTTTAATTTCCTGTT[C/T]GAAGCCTAGAGTTTA	4297
rs181491981	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118471236	AAGCCAGAATTCTGA[A/G]TTGAAAAGATGGGAT	4297
rs181497044	snp	A/G	0.00318978	0.0398085	intron-variant	KMT2A	GRCh38.p7	11:118450062	TGGTACTTTCCTATT[A/G]GAGAAAAATAAACCC	4297
rs181617468	snp	A/G	0.00279162	0.0372561	intron-variant	KMT2A	GRCh38.p7	11:118486642	CTTTGGGAGGCTGAC[A/G]CAGGAGGACCGCTTG	4297
rs181635398	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118514023	AATATAAGTCACATC[C/T]CTTTCTTTTTCTCTG	4297
rs181714445	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118444475	GTAGTGGTGTGAGAT[C/T]GTTTAGCATAGTAAT	4297
rs181715956	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118466279	AGGCTGCAGTGAGCC[A/G]TGATCACACCACTGC	4297
rs181763308	snp	A/G	0.00318978	0.0398085	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118518684	GCTACTTGGGAGGCT[A/G]AGGCAGGAGAATTGC	4297
rs181772677	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118459215	GCTGGGATTAAAGGC[A/G]TGTACCACTATGCCC	4297
rs181775729	snp	C/T	3.3048e-05	0.00406484	intron-variant	KMT2A	GRCh38.p7	11:118480160	GTTTCATGGTTTATT[C/T]GTTGTTTTCCTAGGA	4297
rs181834631	snp	A/G	0.0162398	0.0886349	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118436382	CTCTGCATAGCGGCC[A/G]GCAGGGTGCAGGCGG	4297
rs181901354	snp	G/T	0.00318978	0.0398085	intron-variant	KMT2A	GRCh38.p7	11:118476083	GCTAATTTTGTATTT[G/T]TAGTAGAGACAGGGT	4297
rs181929744	snp	C/T	0.00199481	0.0315187	intron-variant	KMT2A	GRCh38.p7	11:118450619	GAATTATTGTCTTAG[C/T]GCTCTTTAATCCCAA	4297
rs181961282	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118513033	CATTTGAGGCCAGGA[A/G]TTCAAGACCAGCCTG	4297
rs181965620	snp	A/T	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118476391	TAGTTGTTTGTTTGT[A/T]TTTAAGATAGGGTCT	4297
rs181965878	snp	C/G	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118454243	GCTAGGATAAATCCA[C/G]ATTCCTTACTATGGC	4297
rs182155872	snp	G/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118453491	GCTTCCCTCCTCTGC[G/T]TAACTCTCCTGAATA	4297
rs182183744	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118499567	GGCGGGCAGATCACT[C/G]GAGGTTCAGGAGTTG	4297
rs182196067	snp	A/G	0.00199481	0.0315187	intron-variant	KMT2A	GRCh38.p7	11:118500377	TAAAATGTCTAACAA[A/G]CTAACAATATAAGTT	4297
rs182218872	snp	A/C			missense, intron-variant	KMT2A	GRCh38.p7	11:118472339	AAAGAAGCAGCTCAG[A/C]TGCAGGGAAGAAAGG	4297
rs182309277	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118483700	AGCAATTATTTGTCT[G/T]TAAAAATCACCCTTC	4297
rs182313996	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118510380	AGAACTCTGCTTCCC[C/T]CTCCAGCCTTGTTTT	4297
rs182390575	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118451363	ACCATAGGCTCACAA[C/T]ACCATGCCTACTAAT	4297
rs182470418	snp	A/G	0.00398564	0.0444627	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118523026	GTTCCCTGAGCCTGT[A/G]AGCACTCCAGGTGGG	4297
rs182520928	snp	A/T	0.0520825	0.152737	intron-variant	KMT2A	GRCh38.p7	11:118455673	CTTATTATTATTATT[A/T]TTTTTTATTTTTATT	4297
rs182531319	snp	C/T	1.6703e-05	0.00288985	intron-variant	KMT2A	GRCh38.p7	11:118477030	CAGACTTTTGATTTG[C/T]TTGTTGATTATTCTG	4297
rs182531430	snp	A/G	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118445847	GTCTCTACTAAAAAT[A/G]CAAAAATTAGCTGGG	4297
rs182676246	snp	A/T	1.65081e-05	0.00287293	missense, intron-variant	KMT2A	GRCh38.p7	11:118472731	AGAAAATGAGAGTAA[A/T]GATAGGAGAAGCAGA	4297
rs182686716	snp	G/T			intron-variant, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519531	GCAGCCTCTGGCAGA[G/T]TGACTATAGCATAGG	4297
rs182693041	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118440540	CAGTAACTAGTCTTC[A/G]TTTATTAATGTCATA	4297
rs182696916	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118519314	GGTCATTATGAGCAC[A/G]AAATGAAATAACACG	4297
rs182751765	snp	G/T	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118452007	CCAAATGTAATACAT[G/T]AATCAGGAGGGTTTT	4297
rs182756704	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118474321	CAAAGCACAGGTACT[C/G]TTTTCCACCTTGCCT	4297
rs182758319	snp	A/C	0.00676609	0.0577691	intron-variant	KMT2A	GRCh38.p7	11:118495551	ATTGAGTTCTGTGTA[A/C]TTCAGCAATTTTCAA	4297
rs182898701	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118516845	TGCCTTCCTCTGCTG[C/T]GAGCTCCTTAAGAAC	4297
rs182961506	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118487865	AAATCCTATATCAAT[A/G]TGAAAATAACTTATT	4297
rs182962865	snp	C/T	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118494123	TTGCCACAGGTTAAT[C/T]GTGAATTGAATCTCA	4297
rs182965863	snp	A/G/T			intron-variant	KMT2A	GRCh38.p7	11:118463124	CTTACATTTATCTTT[A/G/T]TTTTTTTTTTTTAAA	4297
rs183087916	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118439231	TCAAAATTGAGACTT[C/G]CCTGGTTATATGTAG	4297
rs183095470	snp	A/C	0.00199481	0.0315187	intron-variant	KMT2A	GRCh38.p7	11:118462614	CCCAGGCTGGAGTGC[A/C]GTGGTGCGATCTCGG	4297
rs183148155	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118468523	ACTATCCTCTGTGTA[C/T]TATGCACCAAAGATG	4297
rs183166836	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118489041	GCCTGAGCCAACATG[A/G]TGAAACCCCATCTCT	4297
rs183193316	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118482565	GGAAAAGCCTTATCC[G/T]TGACTTCTATGTAGA	4297
rs183200691	snp	C/T	0.00636936	0.0560724	intron-variant	KMT2A	GRCh38.p7	11:118509388	GCAGTGTTCTTCCAG[C/T]ACATATTGTGTGATC	4297
rs183237345	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118467421	TCAGATGTCTTTGAA[A/G]AGGAGAATTTCAGCC	4297
rs183239854	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118478639	TTATGTATAATTTTT[A/G]TTGGGTCTACTGAAA	4297
rs183240996	snp	A/G	4.94368e-05	0.00497152	missense	KMT2A	GRCh38.p7	11:118503448	AATTACAGGCACCAC[A/G]GAAACGCACAGTCAA	4297
rs183250503	snp	A/G	0.00914312	0.0669923	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118516247	GTGACACAGAGGTGG[A/G]TAGTTGGTGACAGGA	4297
rs183368790	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118515114	GTGAATCAGAATCCC[C/T]GGGCTTGGAGCTGAG	4297
rs183368979	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118456687	AGAACTCTGCCATCT[A/G]CCCTCCTTTTCTTTC	4297
rs183563725	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118478416	TCTGCAACAATGGAA[A/G]TGTTCTATTGGAATA	4297
rs183578164	snp	A/G	0.0023933	0.0345097	utr-variant-3-prime, intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118525168	ACCAAGGGAATCTCC[A/G]CACAAAAGTGCAGAT	4297
rs183682229	snp	A/C/G	0.00358779	0.0422022	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118513163	GCAGGAGGATCACTG[A/C/G]AGCCTAGGAGTATGA	4297
rs183750033	snp	A/G	0.00199481	0.0315187	intron-variant	KMT2A	GRCh38.p7	11:118475462	GGTACGGTGGCTTAC[A/G]CCTGTAATCCCAGCA	4297
rs183751438	snp	C/T	0.0138799	0.0821421	intron-variant	KMT2A	GRCh38.p7	11:118452865	TCTCGAACTCCTGAC[C/T]TCGTGATCTGCCCAC	4297
rs183785164	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118456223	AAACTTTTAGGGCCA[C/T]GCATGGTGGCTAACA	4297
rs183818442	snp	C/G/T	0.0023933	0.0345097	intron-variant	KMT2A	GRCh38.p7	11:118452152	GCTTAAGCGATTCTA[C/G/T]TCCCTCAGCCTCCAA	4297
rs183845014	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118495952	GCAGATGATTGACTT[C/T]GTGAATCCAATTCAC	4297
rs183961365	snp	A/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118466933	GCATAGTGGTGCATG[A/T]ATGTAGTCCGAGCTA	4297
rs183969521	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118479084	TTAAGCATTTATCCT[G/T]TGTATTACAAACAAT	4297
rs183982809	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118449297	GCACAGTGGCTCACA[A/G]CTGTAATACCAGCAC	4297
rs183985126	snp	A/G	0.0023933	0.0345097	upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118526588	TTAGAGAAAAAGAGA[A/G]AAAAAAAAAAGGAAA	4297
rs183996150	snp	A/G	0.00716266	0.059414	intron-variant	KMT2A	GRCh38.p7	11:118453471	AATTTTCAGTATTCT[A/G]TATGGCTTCCCTCCT	4297
rs184015552	snp	A/T	0.00636936	0.0560724	intron-variant	KMT2A	GRCh38.p7	11:118475731	CCGTCTCTAAAAAAA[A/T]AAATAAATAAAATTA	4297
rs184024553	snp	A/G	0.00358779	0.0422022	intron-variant	KMT2A	GRCh38.p7	11:118499104	ACAAAAATACAGCAA[A/G]ATGATAAACTGTTTT	4297
rs184025970	snp	C/T	0.00279162	0.0372561	intron-variant	KMT2A	GRCh38.p7	11:118474871	GGCTCATGCCTGTAA[C/T]CCCATCACTTTGGGA	4297
rs184026673	snp	A/G	0.00119737	0.0244387	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521766	AAGATAGTACTGGGA[A/G]AAATCTGGAAATTTT	4297
rs184033711	snp	A/G	1.71372e-05	0.00292717	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519917	CTTTACTGCTTTATT[A/G]AAGCATTTCTCTAAA	4297
rs184068654	snp	A/G	0.00199481	0.0315187	upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118526188	AACAGTCCATTCCTC[A/G]GATCAGAGAAAAATG	4297
rs184119935	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118444890	AGAAAAGTTTTTGAA[C/T]CTCTCCATACCTCTG	4297
rs184127699	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118487041	TACAAATTATTGCCT[A/G]CTATTCATTTACTAA	4297
rs184166806	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118442713	TAAGAATACCCTTGT[A/G]GGCTCCACTATTTCT	4297
rs184171418	snp	C/T	0.00117861	0.024247	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520892	TGTCTACAGGTATGA[C/T]TAAAATTCTAGAAAG	4297
rs184174394	snp	A/G	0.00398564	0.0444627	intron-variant	KMT2A	GRCh38.p7	11:118485585	AATCTTTCTTTCTGA[A/G]GGAATTATTTGGAAA	4297
rs184311599	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118465673	CCTCACTGGCATCAC[A/G]TATGAGAAGACTGGA	4297
rs184650271	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118491544	TTCCATAACCTGATT[C/T]TCAATAACCAAATTC	4297
rs184665705	snp	C/T	0.00398564	0.0444627	intron-variant	KMT2A	GRCh38.p7	11:118447283	GCCATTTCTAAGTCA[C/T]CATTTATGTTTTATG	4297
rs184713326	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118457984	AATGGCCGATATATA[C/T]TTTAATGAGTGAGTG	4297
rs184781728	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118464691	CATGTCTTTGAAGAA[C/T]TGTAACAGGAGATGA	4297
rs184789325	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118511313	TGGAGAGGGGAGAGT[A/C]AAAGATGACCCTAAA	4297
rs184806319	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118518132	CACCATTACTGTTTC[C/T]ATATCTATTAATAAT	4297
rs184820566	snp	A/T	0.000115393	0.00759493	missense, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118511992	GTCCAGGAAGCTCGA[A/T]CAAATGCCCGCCTAA	4297
rs184856843	snp	C/T	0.000498795	0.0157844	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118435029	CGACCCTCTCCCTCC[C/T]TCCCAAATTCGCCGC	4297
rs184895314	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118465605	ATTACATAGTCTGAG[A/G]GAATCAGACTGAGAC	4297
rs184898825	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118442013	CTCAGAGGCATAACA[C/G]ACTGCAGTGCCTCTC	4297
rs184902576	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118483937	CTCTTGAGAAGCTGA[A/G]GCAGGAGGATCACGA	4297
rs184959184	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118507396	TATTCTAACCTTTAT[A/G]ACCTTAGGTCAGTTT	4297
rs184973989	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118441388	CATAAGGACTTTGGG[G/T]AAGTTGACCAGTTTC	4297
rs185140096	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118458849	CAGTTTGCCTCCTGG[A/T]TATTTCTTCAACTTT	4297
rs185155002	snp	A/C			missense	KMT2A	GRCh38.p7	11:118505508	GTTTCAGAATCCAGC[A/C]AGAGGACAGACCTCA	4297
rs185201958	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118454915	GTGGCCCATAGTTTT[C/T]CAGTCTTCGGTAAAC	4297
rs185207728	snp	A/C	0.00199481	0.0315187	intron-variant	KMT2A	GRCh38.p7	11:118476447	GTGATCCTCTTGTCC[A/C]AGCCTCCTGAGTAGC	4297
rs185209545	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118500511	TTAGCTGGCAGCTTT[C/T]CACACAAACCAGATT	4297
rs185315919	snp	G/T			upstream-variant-2KB	KMT2A	GRCh38.p7	11:118435731	AGTAGAGCGAGGAGG[G/T]GGCAGGAGACCTGCC	4297
rs185498653	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118444128	GAGAATAGTTTTTTC[C/T]TTAGGCTGTCCTTTA	4297
rs185570106	snp	C/T	0.00795532	0.062565	intron-variant	KMT2A	GRCh38.p7	11:118470161	TGCTGCTTCTACTTA[C/T]CTACCAAAAGAGTTT	4297
rs185585437	snp	A/C	0.00119737	0.0244387	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118517869	TGCTTATCTAGAGAC[A/C]ACATTCTTTTTGTTT	4297
rs185614326	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522955	TCGGGTTGTAGGGGA[C/G]ACTGACTGCCTGCTC	4297
rs185632002	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118508076	AAACAAAAAATATAA[A/C]AAGAATTATTTAAAT	4297
rs185640309	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118451641	TGATCCACCCACCTC[A/G]GCCTCCCAAAGTGAA	4297
rs185689787	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118447853	AAATAGGTTTAAACC[A/G]AAATCAGGAGTAGTT	4297
rs185742655	snp	C/T	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118450210	CACCTTTCTTGAGTT[C/T]TTGGTTTTTTTTTTT	4297
rs185742759	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118438566	GGGAAAGATAACAAC[C/G]AGCCGTTTCCTGCGT	4297
rs185748586	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118471377	CTCATCTAAAATTGT[A/T]AGAAAATCAGTTTTG	4297
rs185750613	snp	A/C	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118492829	TTCAGCTTCTTCATA[A/C]TAGGTTTGGAATTAT	4297
rs185757845	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118523163	AGGAAAAAGATTATT[C/T]AAATAGGATTTAAAT	4297
rs185765474	snp	C/T	0.00398564	0.0444627	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118518639	TACAAAAAAATTAGC[C/T]GGGCATGGTGACGTG	4297
rs185771329	snp	A/C	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118487148	AATATTCAGTCTACA[A/C]GTGCCAGGGGTCTAC	4297
rs185883375	snp	C/T	0.0023933	0.0345097	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118523752	CAAAGTCTGGTTTTT[C/T]CTGCCCAACTTCCCC	4297
rs185909130	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118515450	GTAGGGACAGACGTG[C/T]CAGGATTGATTGGTA	4297
rs186141399	snp	A/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519495	AATTTCGAGCTAATA[A/T]GTACTATAATTCACC	4297
rs186178493	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118466755	GGGAGGCTGAGGTGG[C/T]GCCATTGTACTCCAG	4297
rs186178636	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118444665	TTCAGCCTCAACCTC[C/T]AGGGCTCAAGCAATC	4297
rs186196683	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118486652	CTGACGCAGGAGGAC[C/T]GCTTGAGCTCAGGAG	4297
rs186258245	snp	C/T	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118461165	TGGGAGAAATATTCC[C/T]ATTGCTTCGTCACTC	4297
rs186392877	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118466086	TTTAGATTTTTTTTA[A/G]ATTGGGAGGCCAGTA	4297
rs186432076	snp	A/C	0.000115702	0.00760509	synonymous-codon	KMT2A	GRCh38.p7	11:118481941	ATCCAAACAGGCCAC[A/C]ACTCCAGCTTCCAGG	4297
rs186462551	snp	A/C	0	0	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118434857	GTGTCTCCTCCCTTT[A/C]ATTGCTCCTCTCCAG	4297
rs186471007	snp	A/C	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118457386	GATTCTCCGCCTCAG[A/C]CTCCTGAGTAGCTGG	4297
rs186485271	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118478783	TTTTTAAGAGACAGG[A/G]TCTTGCTCTGTTGCC	4297
rs186489777	snp	C/G	0.000692201	0.0185909	synonymous-codon	KMT2A	GRCh38.p7	11:118504346	CCACACAAGTACCCC[C/G]TCCGACAAAAATTTA	4297
rs186509104	snp	A/T	0.00199481	0.0315187	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118513770	ACCTCATCTCTATAT[A/T]AAAAAAAATTGTTTA	4297
rs186509514	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118526237	GATTTTTTTCTGCCC[A/G]TGAATGTTGCCAGTC	4297
rs186541154	snp	C/T	3.30568e-05	0.00406538	synonymous-codon	KMT2A	GRCh38.p7	11:118482465	GGCTCCCCGCCCAAG[C/T]ATCCCTGTAAAACAA	4297
rs186718411	snp	A/T	0.00517822	0.0506191	intron-variant	KMT2A	GRCh38.p7	11:118455674	TTATTATTATTATTT[A/T]TTTTTATTTTTATTT	4297
rs186718622	snp	C/T	0.0123036	0.0774623	intron-variant	KMT2A	GRCh38.p7	11:118485951	AGCCGGGTGTGGTGG[C/T]GGGCGCCTGTAGTCC	4297
rs186733758	snp	C/G	0.000148411	0.00861298	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521430	AAGGTAAGTCTCCCA[C/G]TTGCACTCACACAGT	4297
rs186778395	snp	G/T	0.0103295	0.0711199	intron-variant	KMT2A	GRCh38.p7	11:118509034	CTGTGGCTCATTTTC[G/T]AGCAGTTATTTTGTA	4297
rs186863897	snp	C/T	0.00358779	0.0422022	intron-variant	KMT2A	GRCh38.p7	11:118461936	GAAAGGAGGACTTTT[C/T]TGCAGCACCCTCTTT	4297
rs187111009	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118499737	GTGAGCTGAGATTGC[A/G]CCACTGCATTCCAGC	4297
rs187112243	snp	A/G	0.000399281	0.0141238	missense	KMT2A	GRCh38.p7	11:118505202	AATGGAGTGACCCAA[A/G]AAATCCAATTGACCT	4297
rs187140142	snp	A/T	0.00199481	0.0315187	upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118526696	ATGCTGAAAGCTCTC[A/T]ACGAAAGACTGAATG	4297
rs187176268	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118453743	CTTCACATGAATTAT[C/G]TCACCTAACCTTCAT	4297
rs187278291	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118476357	ATTTAAAATAGTAGT[A/G]TAATTGGGAATAGAA	4297
rs187324386	snp	A/G	0.00914312	0.0669923	intron-variant	KMT2A	GRCh38.p7	11:118446019	CAAAAAAAAGAAAGA[A/G]AAAAAGAAAAGTACA	4297
rs187336836	snp	A/G	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118467655	AAAAATGGCTAAGAC[A/G]GTTAGCACCTGACTC	4297
rs187368344	snp	A/G	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118474501	AGAAAGTGGCAGGAC[A/G]TAACATTCTAAGTAG	4297
rs187368763	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118441806	AGGCACATACTCCTG[C/G]AGGAAATCATCATTC	4297
rs187372921	snp	C/T	3.36185e-05	0.00409977	synonymous-codon	KMT2A	GRCh38.p7	11:118495718	TGGGATGTTACCAAA[C/T]GCAGTGCTTCCACCT	4297
rs187374908	snp	A/G	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118464726	TGGCTTTACCAATAC[A/G]ATCCTGAAAACAAAG	4297
rs187379713	snp	A/G	6.6558e-05	0.00576841	intron-variant, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519583	TTTCCTGTTGACTGC[A/G]CTCCTCACTTCCCTG	4297
rs187393476	snp	A/G	0.00478085	0.0486577	intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118518915	ACTCCGTCTCTACTA[A/G]AAATACGAAAAAAAT	4297
rs187432701	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118450860	TGAATTTCATTAACT[A/G]TTTGGCTTAAGAAGT	4297
rs187509620	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118445373	AGGCCAAGGCAGCTA[A/T]AATGGGGTTGCTACC	4297
rs187572733	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118447528	ATTGGGGTTTTGAAA[C/G]CGATGTTAGGGTATC	4297
rs187577786	snp	C/T	0.00557542	0.0525036	intron-variant	KMT2A	GRCh38.p7	11:118469310	ATCCTCAGATTTACA[C/T]ATTTTGTGTTATGTG	4297
rs187579316	snp	C/T	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118489323	GGACTTGGGCATCCA[C/T]GGACTTTGGTATCCT	4297
rs187584304	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118516941	AATCTCTCTGGTGAG[G/T]GAGAGTTGAACATTC	4297
rs187644535	snp	G/T	0.0023933	0.0345097	intron-variant	KMT2A	GRCh38.p7	11:118463293	AACTTTTTATTACCT[G/T]TTGAATACTTTACCT	4297
rs187649721	snp	C/T	0.00914312	0.0669923	intron-variant	KMT2A	GRCh38.p7	11:118493688	CATGATCTATATTTG[C/T]GATTCTGTTGTTTAT	4297
rs187656844	snp	A/C	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118510744	TTCATCCACCTTTGA[A/C]GGACTAGTAAATGTT	4297
rs187678279	snp	A/G	0.0150606	0.0854603	intron-variant	KMT2A	GRCh38.p7	11:118467352	ACTGCACTCCAGCCT[A/G]GGTGACAGAGCAAGA	4297
rs187919444	snp	A/G	0.00557542	0.0525036	intron-variant	KMT2A	GRCh38.p7	11:118462747	TGTATTTTTTTTAGT[A/G]GAGACAGGGTTTCAC	4297
rs187924929	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118483802	TTTGGGGGGCCAAGG[C/T]GGGAGGATCACTTGA	4297
rs187925402	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118439521	ACCAGAATATTTTAT[A/C]TGTTGGTCTTTGACA	4297
rs187929157	snp	A/T	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118483398	ATTAGCCCGGCGAGG[A/T]GGCGGGCGCCTGTAG	4297
rs187946618	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118509620	TGAATTTGATTAGGA[A/G]ACAAATGGTCACTTC	4297
rs188083816	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118516485	ATTAAATTAAATTAA[C/G]TATGTTTTCTAAAGT	4297
rs188092390	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118479344	TTATTTAAAATAGAT[C/T]GAGATAGTAGCATAA	4297
rs188131432	snp	A/G	0.00517822	0.0506191	intron-variant	KMT2A	GRCh38.p7	11:118437459	CAGCACCTTGCTTTC[A/G]AAAACCCGATGAACC	4297
rs188174972	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118452067	ACGAGGTCTCACTAT[A/G]TTACCTGCGCTGGAG	4297
rs188211846	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118440761	AGTACTCCTGCAGCT[A/G]AAAGGTAGTAGGAGA	4297
rs188216921	snp	A/C/G/T	0.00104575	0.0228433	intron-variant	KMT2A	GRCh38.p7	11:118484339	TTCAGTGATCATAAA[A/C/G/T]TATATTGAGTGTCAA	4297
rs188226419	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118453119	AATCCTTTAAAAAAA[C/T]GCTTGACCCCACGTC	4297
rs188234517	snp	C/T	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118475578	AATCCAAAAAATTAG[C/T]CAGACATGGTGGCAT	4297
rs188240343	snp	C/T	0.00318978	0.0398085	intron-variant	KMT2A	GRCh38.p7	11:118460487	GAGATGGGGGTCTCA[C/T]CATGTTGCCCAGCCT	4297
rs188250633	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118480748	ACTCACTGTAGCTTC[A/G]ACCTCCCACGCTCAA	4297
rs188435877	snp	C/T	3.29587e-05	0.00405934	missense	KMT2A	GRCh38.p7	11:118502896	GAATTCCTAAACTGG[C/T]CCCACAGGTTCATAA	4297
rs188455217	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118487868	TCCTATATCAATATG[A/G]AAATAACTTATTTCT	4297
rs188456718	snp	G/T	0.00398564	0.0444627	intron-variant	KMT2A	GRCh38.p7	11:118458384	GAGCCACCTCGTCCT[G/T]CCCCTATACATTCTT	4297
rs188507661	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118511699	ATTCAGAGTTCATTT[C/T]AGAAGGTCTGACTTT	4297
rs188663067	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118471167	ATGGGACTCTGAGCT[A/G]CCCAAGGAGTTGGTA	4297
rs188664812	snp	A/T	0.0142736	0.0832652	intron-variant	KMT2A	GRCh38.p7	11:118449423	TAAATTTAAAAAATT[A/T]AAAAAAAAAAATTAG	4297
rs188680136	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118492446	GCACTTCGGGAGGCC[A/G]AGGCGGGCGGATCAC	4297
rs188687710	snp	G/T	0.00398564	0.0444627	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118518251	GTGGCAGTTGTAATT[G/T]TGCCCTGTCCCTTTA	4297
rs188721968	snp	C/T	0.00478085	0.0486577	intron-variant	KMT2A	GRCh38.p7	11:118456431	GCAACCTCCGCCTCC[C/T]GGGCTCAAGCAATTC	4297
rs188723449	snp	A/C			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118525304	CTTATAGCTTTGCTG[A/C]TAGAACCTGTTGTGG	4297
rs188890469	snp	A/G	0.00398564	0.0444627	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520668	AAAAAAAAGGGGGGC[A/G]CTCATTTTATAAGGC	4297
rs188907223	snp	C/T	0.00755907	0.0610114	intron-variant	KMT2A	GRCh38.p7	11:118499562	GCTGAGGCGGGCAGA[C/T]CACTGGAGGTTCAGG	4297
rs188913109	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522269	GAGCTCCCGGATTGC[A/G]TGGCACAGCTGAGGG	4297
rs188940970	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118471489	ATTTGCTGACTTCTT[G/T]GAGGCAAATTTTGGG	4297
rs188946751	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118492833	GCTTCTTCATACTAG[C/G]TTTGGAATTATCAAG	4297
rs188958258	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118518651	AGCTGGGCATGGTGA[C/T]GTGCCCCTGTAGTCC	4297
rs188972322	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118475150	AAATAAATAAATAAA[C/T]AAATAAACAAACAGA	4297
rs189000227	snp	A/T	0.0023933	0.0345097	intron-variant	KMT2A	GRCh38.p7	11:118478454	ACAATAATGGAAATG[A/T]TTAGTTCAGTATGCA	4297
rs189001933	snp	A/T	0.0023933	0.0345097	intron-variant	KMT2A	GRCh38.p7	11:118447981	AGTACAGTCCTGCCT[A/T]CATATGTATAAAATG	4297
rs189128796	snp	A/G	0.00137546	0.0261885	intron-variant	KMT2A	GRCh38.p7	11:118491338	GAGTCTTTTTATTTC[A/G]GTTTTCTTCTTTCTA	4297
rs189136239	snp	C/T	0.0193772	0.0965046	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118436205	TTTCCCGAGCAATGC[C/T]TCTCCCGGAGGGCGG	4297
rs189156873	snp	A/T	0.00290179	0.03798	intron-variant	KMT2A	GRCh38.p7	11:118496399	ACAGGGCCCTAGTTA[A/T]TACATACTCCAAAAG	4297
rs189184291	snp	C/G	0.000798403	0.0199641	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118513171	ATCACTGGAGCCTAG[C/G]AGTATGAGACTGTAT	4297
rs189237793	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118452260	AGCTTTTTCAGTCAG[G/T]CATGGTGGCTCACAC	4297
rs189263095	snp	G/T	0.00398564	0.0444627	intron-variant	KMT2A	GRCh38.p7	11:118465919	CTGTTTTTGTTTTGT[G/T]TTGTTTTTTTGGTAA	4297
rs189296114	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118470361	CCAGGCTCTGGGCAG[A/G]AGTTTTATTTTGTTA	4297
rs189416780	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118518046	AACTGTATGTCTGTT[A/G]GAATTGCATATGTGC	4297
rs189532479	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118442828	AGTTTCCAGGACCTT[C/T]GTATTCAAAATACAG	4297
rs189551520	snp	A/G	0.0150606	0.0854603	intron-variant	KMT2A	GRCh38.p7	11:118485910	ACACAGTGAAACCCC[A/G]TCTCTATTAAAAATA	4297
rs189568282	snp	A/G	0.00279162	0.0372561	intron-variant	KMT2A	GRCh38.p7	11:118465612	AGTCTGAGAGAATCA[A/G]ACTGAGACCCTAAAC	4297
rs189572278	snp	A/G	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118442043	CTCTTTTGGAAACTC[A/G]CTGTGTTTTAATTGT	4297
rs189586944	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118485097	TTTAAACCAGCTAAA[A/G]AAATGTTTTGAAGTA	4297
rs189588792	snp	A/T	0.00358779	0.0422022	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512710	AAGTACTGCCAGGTT[A/T]TTTTTCCAAAGTGGC	4297
rs189627778	snp	A/G	0.00755907	0.0610114	intron-variant	KMT2A	GRCh38.p7	11:118483503	GCGCCACTGCACTCC[A/G]GCTTGGGTGACACCG	4297
rs189629718	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118509692	GCTTATTGAAAAACT[A/G]TCAGATCGTCATACT	4297
rs189702894	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118462762	AGAGACAGGGTTTCA[C/T]CGTGTTAGCCAGGAT	4297
rs189706555	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118439944	TTTTTTTTTTTTAAC[A/G]TAGCCTTACTAATCA	4297
rs189787326	snp	C/T			upstream-variant-2KB	KMT2A	GRCh38.p7	11:118435062	CAGGCTGTAATATTA[C/T]ATGCAGTGCGCTGTA	4297
rs189831114	snp	C/T	0.00795532	0.062565	intron-variant	KMT2A	GRCh38.p7	11:118453477	CAGTATTCTGTATGG[C/T]TTCCCTCCTCTGCTT	4297
rs189848221	snp	A/G	0.00755907	0.0610114	intron-variant	KMT2A	GRCh38.p7	11:118455299	TGTATCTTGAGAGTC[A/G]AACAGTACCTGGCAA	4297
rs189868629	snp	C/T	0.00199481	0.0315187	intron-variant	KMT2A	GRCh38.p7	11:118500538	GATTCCACTAGCATT[C/T]AGCAGATTTGAAGCA	4297
rs189880899	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118523190	AAATCATGCAACAAC[A/G]AGAGTATCACAGCCA	4297
rs190072394	snp	A/C/T			intron-variant	KMT2A	GRCh38.p7	11:118458861	TGGATATTTCTTCAA[A/C/T]TTTAGTTGTTCTCAG	4297
rs190087851	snp	A/G	9.89495e-05	0.00703313	synonymous-codon	KMT2A	GRCh38.p7	11:118506125	AGGAATGTTTCCACA[A/G]CTGGGGACATCACAG	4297
rs190105887	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118451762	CTCTCAAAGTGCTGG[G/T]ATTATAGGTGCGACC	4297
rs190124475	snp	A/C	0.000399281	0.0141238	intron-variant, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519528	GGAGCAGCCTCTGGC[A/C]GAGTGACTATAGCAT	4297
rs190193631	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118476047	AGTAGCTGGGATTAC[A/G]GGCATGCACCACCAC	4297
rs190232444	snp	C/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118513874	GCCTGGGAGGTCAAG[C/T]CTACAGTGAGCCAAG	4297
rs190236402	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522964	AGGGGAGACTGACTG[A/C]CTGCTCAAGGACACT	4297
rs190327077	snp	C/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118450448	TTGACATGGAGTGGG[C/G]ATGAGGGGTACTACC	4297
rs190329497	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118479714	CATTTGAATTTTATT[A/G]AATCTAAATTTAGGG	4297
rs190455363	snp	A/C	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118444170	TTCTAAACACTAGGG[A/C]AAAGTTAATTCTTAT	4297
rs190473004	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118466103	TTGGGAGGCCAGTAT[A/G]GGAGGATCACTTGAG	4297
rs190478808	snp	A/G	0.00398564	0.0444627	intron-variant	KMT2A	GRCh38.p7	11:118486592	GTAAAGAAAATCCAC[A/G]TCGGGTGCAGTGGCT	4297
rs190505891	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118438770	CTCCTTTTTTTTAAT[C/T]GTTTCTAAGGCAGCC	4297
rs190518681	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118476381	AATAGAAGCTTAGTT[A/G]TTTGTTTGTTTTTAA	4297
rs190524628	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118462064	GTTCAAGTAATTCTC[A/G]TGCCTCAGCCTCCCG	4297
rs190528642	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118482553	TCTATTTTGTAGGGA[A/G]AAGCCTTATCCTTGA	4297
rs190548021	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118524284	GTGTAGTCCAAGTAG[A/T]GGGTGGGGCACCCTT	4297
rs190750820	snp	C/T	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118466777	GTACTCCAGCCTGGG[C/T]GACAGAGCAAGACTC	4297
rs190751669	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118451295	CAGCTCACTGCAGCC[G/T]CAAACTCCTGGGCTC	4297
rs190755170	snp	A/G	0.00716266	0.059414	intron-variant	KMT2A	GRCh38.p7	11:118486946	GGTTGAAATCTGAAT[A/G]TTGAGCAGTCAGTGA	4297
rs190759246	snp	A/G	0.00795532	0.062565	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118514869	AACTCCTGACCTCAG[A/G]TAATCTGCCCGCCTC	4297
rs190767682	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118453844	GGATACCTAATAGGT[A/G]TCTCTTACTTACCAT	4297
rs190770247	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118493893	ATTTTGTATTTTTGG[C/T]GGAGATTGGGTTTCA	4297
rs190783803	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118500089	TTGGGACTATGTTAG[C/T]GGAATCCAGTTATAG	4297
rs190806091	snp	C/T	0.00755907	0.0610114	intron-variant	KMT2A	GRCh38.p7	11:118467415	ACTTTTTCAGATGTC[C/T]TTGAAGAGGAGAATT	4297
rs190935037	snp	A/G	0.00676609	0.0577691	intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118519147	ACATAAGCTTATAGA[A/G]CCTAGATAATCCATT	4297
rs191014566	snp	C/T	0.000330546	0.0128516	missense, intron-variant	KMT2A	GRCh38.p7	11:118472678	GAGCGGAGCGATACC[C/T]CTGAAGTTCATCCTC	4297
rs191043573	snp	A/G	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118445646	TGGAACTTGAGCAGA[A/G]TGGTCAAAAGCAGAT	4297
rs191072295	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118487525	CAAATTCCCTAAGTG[A/T]TAATATGTTTCTCTG	4297
rs191201819	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118452448	GAGATGGGAGCATCA[C/T]TTAAGCCCAGGAATA	4297
rs191277635	snp	G/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118508079	CAAAAAATATAACAA[G/T]AATTATTTAAATAAT	4297
rs191307994	snp	A/C	0.0092418	0.067346	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118435004	AGAGCTGAGTGCAAC[A/C]TGCTCACAACGACCC	4297
rs191317739	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118438262	GATGAAGGGTCAGAG[A/C]GTTGCCCCTTCCCCA	4297
rs191329636	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118482174	AACAGCATTTGAAAG[C/T]AGGAAATGTATGATT	4297
rs191446381	snp	A/G	3.29587e-05	0.00405934	missense	KMT2A	GRCh38.p7	11:118504879	ACATGACTCCTGATC[A/G]TTTTATCCAAGGACA	4297
rs191454309	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118526465	TGAATAATTGTTTCA[A/G]GAGCTCAACAGATGA	4297
rs191483551	snp	A/G	0.000214226	0.0103473	synonymous-codon	KMT2A	GRCh38.p7	11:118501802	CCCCAGGATTCGAAC[A/G]CCCAGTTATTCTCCA	4297
rs191500081	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521715	CCTCTAGACTAGTGG[C/T]CTGTAATCTAGGAAA	4297
rs191559762	snp	A/G	0.0170251	0.090679	intron-variant	KMT2A	GRCh38.p7	11:118455680	TTATTATTTTTTTTT[A/G]TTTTTATTTTTATTT	4297
rs191566875	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118461452	AGTTAACAGTATTTT[A/G]CAGTGCTCTACTTGG	4297
rs191576793	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118453132	AACGCTTGACCCCAC[A/G]TCCACCTCTAGCTGC	4297
rs191613432	snp	C/T	0.000852641	0.0206299	intron-variant	KMT2A	GRCh38.p7	11:118509090	GGTTTTTTCTTTGAA[C/T]TGAAGAACTAGCTGA	4297
rs191850647	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118478378	AGAAATACTCTGGGG[C/G]CATGCTGTCATTAAT	4297
rs191853604	snp	C/T	0.00517822	0.0506191	intron-variant	KMT2A	GRCh38.p7	11:118478614	GATTTCTACTTAAAA[C/T]CTGACAACTTTATGT	4297
rs191872671	snp	A/G	0.00358779	0.0422022	upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118526163	ACCTCTAACCATAAA[A/G]GAATGGTAGAACAGT	4297
rs192063424	snp	A/G	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118446094	TGGCTCAATCCTGTA[A/G]TCCCAACACTTTGGA	4297
rs192066946	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118468424	GTATTGGGGCTGTAT[A/G]TTTCTGCCATTATAC	4297
rs192081955	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118488862	TATCTGGGAAAAAAT[G/T]AGTAGTTGCCTCTGT	4297
rs192084444	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118444827	TGGTCCCCCTACCTC[A/C]GCCTCCCAAAGTGTT	4297
rs192089018	snp	A/G	0.00119737	0.0244387	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118516650	CCTAAGGTCCTGTCT[A/G]GCACAGTGGAAAGAT	4297
rs192173056	snp	A/G	0.000131796	0.00811668	synonymous-codon	KMT2A	GRCh38.p7	11:118502975	ACCCTCTTCAGTGTC[A/G]TTTTCTTCTAAAGAG	4297
rs192198576	snp	G/T	0.0023933	0.0345097	intron-variant	KMT2A	GRCh38.p7	11:118441977	CTGTGGCTAGAGGGG[G/T]TGGCAACAGTGCTTT	4297
rs192245846	snp	G/T	1.65883e-05	0.00287991	intron-variant	KMT2A	GRCh38.p7	11:118496418	ATACTCCAAAAGAAC[G/T]GTTTGTCCTTGTGTC	4297
rs192307705	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118464937	TAACCAAAGCTTTAG[C/T]AGAAAAATGCCCAGG	4297
rs192315937	snp	A/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519609	CCCTGGTGCTTCTGA[A/T]TCTTCTAGGTGTTAA	4297
rs192318191	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118484723	TAAAACTTTTTAAAG[C/T]AGCAGTTATTTTTGG	4297
rs192329155	snp	G/T	0.00159617	0.0282053	intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118511890	TTGTGCACATCATTG[G/T]TATTAAGAAGGGTTT	4297
rs192369191	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118456573	TCAAACTCCTGACCT[C/T]ATGATTCGCCCACCT	4297
rs192437990	snp	A/C	0	0	intron-variant	KMT2A	GRCh38.p7	11:118489610	CTCATCACTGAGTGC[A/C]TTTGGCAGGAAATAA	4297
rs192498323	snp	C/T	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118470438	ACTACCAGTCTACCT[C/T]GAATGTTGTCTTGTT	4297
rs192508140	snp	C/T	0.00159617	0.0282053	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118518067	GCATATGTGCAATTG[C/T]AGTCCTAATACAATT	4297
rs192583814	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118440928	AGTGCACGAAGCCTC[C/T]GAGTAGAAGTCAGTG	4297
rs192604302	snp	C/T	0.00636936	0.0560724	intron-variant	KMT2A	GRCh38.p7	11:118483919	CACCTGTAGTCCCAG[C/T]TACTCTTGAGAAGCT	4297
rs192652720	snp	G/T	0.00755907	0.0610114	intron-variant	KMT2A	GRCh38.p7	11:118475263	GACCAGCATTTTTGT[G/T]TTTTTTTTATTGTTT	4297
rs192792879	snp	C/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118449293	CTGGGCACAGTGGCT[C/G]ACAACTGTAATACCA	4297
rs192803019	snp	G/T	0.00676609	0.0577691	intron-variant	KMT2A	GRCh38.p7	11:118491442	TAAATTTATTTTTTA[G/T]TCTCTAGAATAAGCA	4297
rs192855784	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118464536	AAGAGGGAAACTCTG[C/T]CTCAAAAAAAAAAAA	4297
rs192863035	snp	C/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118510968	CATTTGGTGGGTTTA[C/G]AGTAGTGTCAGGTGA	4297
rs192869509	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118458690	TGTGAGCATGTCTTT[A/C]AGGTGCAACATTAAG	4297
rs192922463	snp	A/G	0.00318978	0.0398085	intron-variant	KMT2A	GRCh38.p7	11:118474679	CCTTATAAGTTTGAT[A/G]TAATTAAACCAGGGA	4297
rs192938390	snp	C/T	0.00438332	0.0466095	upstream-variant-2KB, downstream-variant-500B, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118527101	AACAGGGCCTTTACC[C/T]TCTACATAGCTCCCC	4297
rs193039912	snp	C/T	0.0178098	0.0926698	intron-variant	KMT2A	GRCh38.p7	11:118447852	AAAATAGGTTTAAAC[C/T]GAAATCAGGAGTAGT	4297
rs193072190	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118435632	CACCGCGTCGTTAGC[A/G]GAGCACGCCGTGGCC	4297
rs193076362	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118479415	ACAAATAATAGGTGT[A/C]AATAGATATTTGCTG	4297
rs193161441	snp	A/C	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118452132	TTACAGACTTGAAAT[A/C]CTGAGCTTAAGCGAT	4297
rs193192906	snp	C/T	1.67379e-05	0.00289287	missense	KMT2A	GRCh38.p7	11:118495879	CTCTGCATCCTCCTA[C/T]ACCACCAATTTTGAG	4297
rs193226713	snp	C/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118469902	GGGGGCAGTTGGCCA[C/G]TAGTGTCCCAGTATC	4297
rs199551818	snp	C/T	0.000125903	0.00793319	intron-variant	KMT2A	GRCh38.p7	11:118490280	AGTTTTGCCAGCTTT[C/T]GGAGGTTGTACTTGG	4297
rs199606724	snp	A/G	1.64776e-05	0.00287028	synonymous-codon	KMT2A	GRCh38.p7	11:118502549	TCCAATGAGAACTGG[A/G]AATACTTACTCTAGG	4297
rs199612120	snp	A/G	0.0024693	0.0350507	intron-variant, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512037	GCAGGTAATGGCTGG[A/G]GGTGTTATTCCACTC	4297
rs199620348	snp	G/T	1.64754e-05	0.00287009	missense	KMT2A	GRCh38.p7	11:118476842	AGACCTCTGTGCGAG[G/T]ACCCCGGATTAAACA	4297
rs199656572	snp	C/G	0.000494112	0.0157102	missense	KMT2A	GRCh38.p7	11:118506483	CAGCGGTCAGCAAGC[C/G]CTTCAGTGCCGGGTC	4297
rs199659721	snp	C/G	3.29603e-05	0.00405944	synonymous-codon	KMT2A	GRCh38.p7	11:118506185	ATCTAGCATCTGTGT[C/G]CTCCCCTCCACTCAG	4297
rs199777895	in-del	-/CGTCTCTCGGG			intron-variant	KMT2A	GRCh38.p7	11:118437389	AGTTTTCCTCTCGGG[-/CGTCTCTCGGG]TGATGGCCTCATCCA	4297
rs199805835	in-del	-/T			intron-variant	KMT2A	GRCh38.p7	11:118483374	TGTCTCTACTAAAAA[-/T]ACAAAAAAATTAGCC	4297
rs199821596	snp	C/T	6.9856e-05	0.00590958	intron-variant	KMT2A	GRCh38.p7	11:118491964	TTCTGAGAGCTTGTT[C/T]TTAGGTAGTCTTTAC	4297
rs199822229	snp	C/T	1.65416e-05	0.00287586	missense	KMT2A	GRCh38.p7	11:118474259	AAGGCCAAAGCTCAG[C/T]TCTGCAAGATTGAGA	4297
rs199851071	snp	C/T	0.000216603	0.0104046	synonymous-codon	KMT2A	GRCh38.p7	11:118509175	TCAGGTGACCCAAAA[C/T]CCAGCAAATGAACAA	4297
rs199853158	snp	A/G	0.000116812	0.00764148	intron-variant	KMT2A	GRCh38.p7	11:118500945	CTAGTTTCTGCTTCT[A/G]TCCTCTCCCTTATGA	4297
rs199861855	in-del	-/G	0.0134861	0.0810011	intron-variant	KMT2A	GRCh38.p7	11:118486373	TTTATTTGTTTCTCT[-/G]GGTTTTTTTTTTTTA	4297
rs199868811	snp	C/T	0.00199792	0.0315431	missense	KMT2A	GRCh38.p7	11:118501067	TGGAGTGCCGTCCTC[C/T]AGTCGTAGAGCCGGA	4297
rs199922480	snp	C/G	6.59783e-05	0.00574324	missense, intron-variant	KMT2A	GRCh38.p7	11:118473476	TCACCTCTCACCCCC[C/G]CGTCTTCTGTCTCTT	4297
rs200008889	snp	A/G	3.30344e-05	0.004064	synonymous-codon	KMT2A	GRCh38.p7	11:118503110	AGTCAAAACCTTGAA[A/G]CTATCTGGAATGAGC	4297
rs200069252	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118484035	GACCCAGTCTCTTTT[-/A]AAAAAAAAATTCAAA	4297
rs200074613	in-del	-/T			intron-variant	KMT2A	GRCh38.p7	11:118458054	CATTCTCCCTATGCA[-/T]TTTTTTTTTGAGATG	4297
rs200088623	snp	G/T	6.61376e-05	0.00575017	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521243	TCACGCACTTAACCT[G/T]ACTTGCAAAATTTGT	4297
rs200112360	snp	G/T			missense	KMT2A	GRCh38.p7	11:118506213	CAGACTACGGGCATA[G/T]CAGCCGCTTCACCTT	4297
rs200127166	snp	A/G	0.000230631	0.010736	missense	KMT2A	GRCh38.p7	11:118498049	AAAGAATGTGCATAT[A/G]GCTGTGATCAGGGGC	4297
rs200134640	snp	A/G	0.00041175	0.0143424	missense, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521367	GAGTATGCCGGCAAC[A/G]TCATCCGCTCCATCC	4297
rs200141649	snp	C/T	4.94376e-05	0.00497156	missense	KMT2A	GRCh38.p7	11:118505220	ATCCAATTGACCTCT[C/T]CTGTTAGTTCTACAC	4297
rs200146007	snp	G/T	0.003992	0.0444979	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521842	ATTGGGACATGTTCT[G/T]AAAGCTGAGTTTATA	4297
rs200153433	snp	A/T	0.00199481	0.0315187	intron-variant	KMT2A	GRCh38.p7	11:118463128	CATTTATCTTTATTT[A/T]TTTTTTTTAAATAAA	4297
rs200177201	snp	G/T	0.00199792	0.0315431	missense	KMT2A	GRCh38.p7	11:118503983	TTCTTCAGGTGGAGA[G/T]GAACGACTGGCATCC	4297
rs200178227	snp	A/G	0.000221569	0.0105231	intron-variant	KMT2A	GRCh38.p7	11:118495912	AGCCACCAAAAGGAG[A/G]GTCGTCACCCATTTC	4297
rs200209840	snp	C/T	1.64732e-05	0.0028699	missense, intron-variant	KMT2A	GRCh38.p7	11:118474137	CCCTCTGCCTTTCCA[C/T]TCCTTCATCTAGCAC	4297
rs200232275	snp	A/G	8.25948e-05	0.00642577	intron-variant	KMT2A	GRCh38.p7	11:118499814	TAATCTTCTCTAATC[A/G]GTTCTTCTTTCCTTG	4297
rs200238069	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118470277	CTTTTGATGTATTTC[C/T]GGGCAGGAGTTGTTT	4297
rs200242242	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118514668	GACAGAGTTTCTTTC[C/T]TGTTGCCCAGGCTGG	4297
rs200249108	snp	C/T	6.6024e-05	0.00574523	intron-variant	KMT2A	GRCh38.p7	11:118499922	GATATCAGTAAGTAG[C/T]ACTATAAAGAGAAGA	4297
rs200260418	snp	C/G	1.64746e-05	0.00287002	missense	KMT2A	GRCh38.p7	11:118506272	TCAGCATGTGAACCA[C/G]CTCCTTGCCAGCAAA	4297
rs200324977	snp	C/T	0.00199792	0.0315431	missense	KMT2A	GRCh38.p7	11:118505721	TTAGATTTGGGGTCA[C/T]TTAATACTTCATCTC	4297
rs200365395	snp	A/G	0.00023062	0.0107358	synonymous-codon	KMT2A	GRCh38.p7	11:118505969	CCCTACAAGTAGTGC[A/G]TCAGTTCCAGGACAC	4297
rs200371479	snp	A/C/T	1.64754e-05	0.00287009	missense	KMT2A	GRCh38.p7	11:118506498	CCTTCAGTGCCGGGT[A/C/T]CCACTAAACCCAAAC	4297
rs200372591	snp	C/T	0.000689564	0.0185555	intron-variant	KMT2A	GRCh38.p7	11:118498571	AAAAAAAAAAGACTT[C/T]TTTAGAGCAGTTTTA	4297
rs200497972	snp	A/C	0.000132536	0.00813943	synonymous-codon	KMT2A	GRCh38.p7	11:118502463	CTCTCCTCTGGACTT[A/C]GAAGCATTGGCTCCA	4297
rs200547771	snp	A/C	0.00299558	0.0385852	intron-variant	KMT2A	GRCh38.p7	11:118498341	CATATGAAAGTCTGA[A/C]TAGGACTCTGTTCTT	4297
rs200569641	snp	C/G			intron-variant, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521257	TTACTTGCAAAATTT[C/G]TGTCTGACCTCTTTT	4297
rs200575492	snp	C/T	1.65274e-05	0.00287462	intron-variant	KMT2A	GRCh38.p7	11:118493260	TGAGCCATCAGAATT[C/T]CTAGTGCCAATAAAG	4297
rs200576371	snp	C/T	0.000181188	0.00951636	synonymous-codon, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521360	GGTGATTGAGTATGC[C/T]GGCAACGTCATCCGC	4297
rs200597062	snp	C/T	4.94311e-05	0.00497123	synonymous-codon, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519766	CTTGAACCCTCACGG[C/T]TCAGCCAGGGCTGAA	4297
rs200600434	snp	A/G	4.94295e-05	0.00497115	missense, intron-variant	KMT2A	GRCh38.p7	11:118473843	AAGAGAAAAGGAAAA[A/G]GGGATCAGAAATTCA	4297
rs200629846	snp	C/T	1.65042e-05	0.0028726	synonymous-codon	KMT2A	GRCh38.p7	11:118488730	TTGCAAATTCTGTCA[C/T]GTTTGTGGAAGGCAA	4297
rs200633378	snp	C/T	0.00199806	0.0315443	missense	KMT2A	GRCh38.p7	11:118502830	GAGAGAAGACCAAAG[C/T]GCTGAGTTCCAAGAG	4297
rs200690158	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118463137	TTATTTTTTTTTTTT[-/A]AATAAAGATGGGGTC	4297
rs200698383	snp	A/G	1.67542e-05	0.00289427	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118471948	GACACCTTCTGCTAC[A/G]TTTCAGCAAGCCACA	4297
rs200708161	snp	A/G	3.30595e-05	0.00406554	synonymous-codon	KMT2A	GRCh38.p7	11:118482474	CCCAAGTATCCCTGT[A/G]AAACAAAAACCAAAA	4297
rs200726332	snp	G/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118518243	AAAGAAGTGTGGCAG[G/T]TGTAATTGTGCCCTG	4297
rs200727599	snp	C/G	0.000504589	0.0158758	synonymous-codon	KMT2A	GRCh38.p7	11:118490239	TGATTGCGCCAAGCT[C/G]TTTGCTAAAGGTACC	4297
rs200739718	snp	G/T	3.29516e-05	0.00405891	missense	KMT2A	GRCh38.p7	11:118505150	CATAGTTGTTAACCA[G/T]AACATGCAGCCACTT	4297
rs200775587	snp	A/G/T	6.71958e-05	0.00579605	intron-variant	KMT2A	GRCh38.p7	11:118476778	ACATGTATGGTTGTT[A/G/T]TTGTTTTTGGATTGC	4297
rs200807035	snp	A/G	0.00119391	0.0244035	intron-variant	KMT2A	GRCh38.p7	11:118477929	ACCAGGTTTGAATTC[A/G]GTACTCCCTTGGAAC	4297
rs200854315	snp	A/G	8.36113e-05	0.00646519	intron-variant	KMT2A	GRCh38.p7	11:118493026	TTGGTTTTAGTGTTA[A/G]ATAAAAGCAACATAT	4297
rs200865931	snp	C/G	0.000232196	0.0107724	intron-variant	KMT2A	GRCh38.p7	11:118482503	AAGAAAAGGTGAGGA[C/G]AGATTTGTTTCTCTG	4297
rs200897156	snp	C/T	1.64806e-05	0.00287054	intron-variant	KMT2A	GRCh38.p7	11:118488604	CTATCTTCCCATGTT[C/T]TTACTATAGTTTGTG	4297
rs200914297	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118452053	TGTTTTTTTAAGAGA[C/T]GAGGTCTCACTATGT	4297
rs200927500	snp	A/C	0.000715003	0.0188942	missense	KMT2A	GRCh38.p7	11:118505532	GACCTCAGTACCACA[A/C]TAGCCACTCCATCCT	4297
rs200935930	snp	C/T	3.29614e-05	0.00405951	synonymous-codon	KMT2A	GRCh38.p7	11:118502495	GCGTCACAGTACCTC[C/T]TCCTTATCACCCCAG	4297
rs200946943	snp	C/G	0.000399281	0.0141238	missense, intron-variant	KMT2A	GRCh38.p7	11:118473507	CCTCGTTAAGCATTT[C/G]TGTTAGTCCTCTTGC	4297
rs201036125	in-del	-/A	0.0170251	0.090679	intron-variant	KMT2A	GRCh38.p7	11:118485507	AAATTAAAGCATGAT[-/A]AAAAAAAGAATCCTG	4297
rs201067303	snp	C/T	0.000399281	0.0141238	synonymous-codon	KMT2A	GRCh38.p7	11:118510093	CAGTGATGATGGCTT[C/T]CAGATCTGTGCAGAA	4297
rs201093582	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118467304	ATCGCTTGAACCCAG[A/G]AGGCGGAGGTTGCAG	4297
rs201104615	in-del	-/T			intron-variant	KMT2A	GRCh38.p7	11:118445059	AGCAGGGTTATAATC[-/T]TTTTTTTTTCATCAA	4297
rs201139747	snp	G/T	0.000399281	0.0141238	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118472680	GCGGAGCGATACCCC[G/T]GAAGTTCATCCTCCA	4297
rs201155865	snp	C/T	0.000399281	0.0141238	missense	KMT2A	GRCh38.p7	11:118436799	CTTCGTCTTCGTCAT[C/T]GTCCTCAGCCTCTTC	4297
rs201228089	in-del	-/C			intron-variant	KMT2A	GRCh38.p7	11:118483229	AGAGCTAGACTCCAT[-/C]CCCAAAAAAAAAAAA	4297
rs201233324	snp	C/G	0.00199801	0.0315438	intron-variant	KMT2A	GRCh38.p7	11:118477006	AGAAGGTCAATCTTG[C/G]AGTCGGAACAGACTT	4297
rs201281130	snp	A/G	0.000197811	0.00994315	synonymous-codon	KMT2A	GRCh38.p7	11:118504337	CCGCAGAGTCCACAC[A/G]AGTACCCCCTCCGAC	4297
rs201345346	snp	A/G	0.000164769	0.0090751	missense	KMT2A	GRCh38.p7	11:118506219	ACGGGCATAACAGCC[A/G]CTTCACCTTCTGGGG	4297
rs201348021	snp	A/G	0.00289989	0.0379676	intron-variant	KMT2A	GRCh38.p7	11:118498567	AAAAAAAAAAAAAAG[A/G]CTTTTTTAGAGCAGT	4297
rs201363598	snp	A/G	0.00498744	0.0496875	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521830	CATCAAGAGAAGATT[A/G]GGACATGTTCTTAAA	4297
rs201377865	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118495164	TTTATTTATTTATTT[-/A]TTTTTTTTTTTTTGA	4297
rs201380680	in-del	-/AN			intron-variant	KMT2A	GRCh38.p7	11:118502315	TAAATATATATATAT[-/AN]ATAGTCAAATCATTG	4297
rs201391355	snp	A/C	0.00299544	0.0385843	intron-variant	KMT2A	GRCh38.p7	11:118437471	TTCGAAAACCCGATG[A/C]ACCCTCGCGCCATCC	4297
rs201447376	snp	C/T	0.000576412	0.0169668	missense	KMT2A	GRCh38.p7	11:118505839	GAACTGCTGCCACAG[C/T]GGCAGGCACATCAAC	4297
rs201461822	snp	C/T	6.62504e-05	0.00575507	intron-variant	KMT2A	GRCh38.p7	11:118499796	AAAATAAAATGACGC[C/T]CATAATCTTCTCTAA	4297
rs201483860	snp	C/T	0.00107387	0.023147	synonymous-codon	KMT2A	GRCh38.p7	11:118502468	CTCTGGACTTCGAAG[C/T]ATTGGCTCCAGGCGT	4297
rs201494411	snp	A/T	0.000399281	0.0141238	synonymous-codon	KMT2A	GRCh38.p7	11:118490194	CAAAGGGTGGGATGC[A/T]CAGTGGTCTCATGAT	4297
rs201542632	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118515781	GCAACCTCCGCCTCC[C/T]GGGTTCAAGCAATAC	4297
rs201569160	snp	A/G	3.36661e-05	0.00410267	intron-variant	KMT2A	GRCh38.p7	11:118476772	ATTTCAACATGTATG[A/G]TTGTTATTGTTTTTG	4297
rs201616070	in-del	-/T			intron-variant	KMT2A	GRCh38.p7	11:118495160	GATTTTATTTATTTA[-/T]TTTATTTTTTTTTTT	4297
rs201653626	snp	A/G	0.000728573	0.0190724	intron-variant	KMT2A	GRCh38.p7	11:118477011	GTCAATCTTGGAGTC[A/G]GAACAGACTTTTGAT	4297
rs201724179	snp	C/T	0.000131841	0.00811808	synonymous-codon, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522142	GCCCTGCAACTGTGG[C/T]GCCAAGAAATGCCGG	4297
rs201724738	snp	A/G	0.000131876	0.00811915	missense	KMT2A	GRCh38.p7	11:118510031	CAAAAGCGGAAGGAA[A/G]GCATTACTGAGAAAA	4297
rs201733392	snp	C/T	1.64741e-05	0.00286998	synonymous-codon	KMT2A	GRCh38.p7	11:118506446	CTCTCCTGGGGGTTC[C/T]CCATCCTCTCCATCT	4297
rs201740733	snp	C/T	1.65515e-05	0.00287671	missense, intron-variant	KMT2A	GRCh38.p7	11:118472618	CCCAGTGTTGATACC[C/T]CCACAGACTCTCAGG	4297
rs201742004	snp	A/C/G/T	8.76549e-05	0.00661976	intron-variant	KMT2A	GRCh38.p7	11:118491961	TTTTTCTGAGAGCTT[A/C/G/T]TTCTTAGGTAGTCTT	4297
rs201765973	snp	A/G	0.000345893	0.0131464	missense	KMT2A	GRCh38.p7	11:118488650	TGTGAGCCCTTCCAC[A/G]AGTTTTGTTTAGAGG	4297
rs201783253	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118509899	TACATGTAGTCAGTG[C/T]TCAGTGAGCATTTGT	4297
rs201784858	snp	A/G	1.71067e-05	0.00292456	synonymous-codon	KMT2A	GRCh38.p7	11:118490218	TCATGATTTCTCACT[A/G]TGTCATGATTGCGCC	4297
rs201813757	snp	A/C	0.000399281	0.0141238	missense	KMT2A	GRCh38.p7	11:118482470	CCCGCCCAAGTATCC[A/C]TGTAAAACAAAAACC	4297
rs201862340	snp	A/T	1.73468e-05	0.00294501	intron-variant	KMT2A	GRCh38.p7	11:118507494	CATATTTACTGGTGG[A/T]TTGTCTTGAAAAGAT	4297
rs201869352	snp	A/G	3.29495e-05	0.00405877	missense	KMT2A	GRCh38.p7	11:118502946	AATGTTAGTAAAATC[A/G]GCTCCTTTGCTGAAC	4297
rs201876561	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118509292	TTATTTTCTACATTT[-/A]AAAAAAAAAAATCTA	4297
rs201886469	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118466798	GCAAGACTCTGCCTC[-/A]AAAAAAAACAAAACA	4297
rs201921171	snp	A/G	1.64825e-05	0.00287071	missense	KMT2A	GRCh38.p7	11:118505415	GCAGCTACTCAAAGT[A/G]GTTTCCCACCAAACA	4297
rs201960342	snp	C/T	1.64982e-05	0.00287208	missense, intron-variant	KMT2A	GRCh38.p7	11:118473495	CTTCTGTCTCTTCCT[C/T]GTTAAGCATTTCTGT	4297
rs202002114	snp	A/T	1.64732e-05	0.0028699	synonymous-codon	KMT2A	GRCh38.p7	11:118499359	TGTGGACTTTGAAGG[A/T]ATCAGCTTGAGAAGG	4297
rs202043482	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118453401	CCACTCCCTTCTTGG[A/T]TTTTTTTTTTTAACA	4297
rs202054321	in-del	-/A	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118467020	GCAAAATATGTAATT[-/A]AAAAAAAAATTACTG	4297
rs202074087	snp	A/C/G	0.000644605	0.0179427	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521858	AAAGCTGAGTTTATA[A/C/G]GAAATGACAAGTTCT	4297
rs202080031	in-del	-/TTTTG/TTTTGTTTTG	0.0127182	0.0789156	intron-variant	KMT2A	GRCh38.p7	11:118462312	GGCTTTACTTAGTTT[-/TTTTG/TTTTGTTTTG]TTTTGTTTTGTTTTG	4297
rs202162367	snp	A/G	0.00697554	0.058644	intron-variant	KMT2A	GRCh38.p7	11:118498310	GTCTATAGAGGAGAC[A/G]GTAAACGTCTTAAAA	4297
rs202163335	snp	A/G	0.000399281	0.0141238	missense	KMT2A	GRCh38.p7	11:118505493	GATCCCCAACTTTTG[A/G]TTTCAGAATCCAGCC	4297
rs202184506	snp	C/T	0.000228445	0.010685	intron-variant	KMT2A	GRCh38.p7	11:118488777	TACAAAACTTGGTAA[C/T]AGAACTACAGCTGGG	4297
rs202187224	snp	C/T	1.65201e-05	0.00287398	intron-variant	KMT2A	GRCh38.p7	11:118496404	GCCCTAGTTAATACA[C/T]ACTCCAAAAGAACTG	4297
rs202232120	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118467309	TTGAACCCAGGAGGC[G/T]GAGGTTGCAGTGAGC	4297
rs367597386	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118482582	GACTTCTATGTAGAT[A/G]GCAGTGGAATTTCTT	4297
rs367599045	snp	A/T	0.000153988	0.00877328	missense	KMT2A	GRCh38.p7	11:118503706	ACCTAATGCTTCCAG[A/T]TGGCCCCAAACCTCA	4297
rs367630393	snp	C/T	1.66615e-05	0.00288626	intron-variant	KMT2A	GRCh38.p7	11:118482526	TTTCTCTGCCATTTC[C/T]CAGGGATGTATTCTA	4297
rs367660449	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118475967	CTGGAGTGCAATGGC[A/G]TGATCTTGGCTCACT	4297
rs367729437	snp	A/G	0.000153988	0.00877328	intron-variant	KMT2A	GRCh38.p7	11:118499466	CTGTATATATCATTG[A/G]GGAAATTTCTGGTCC	4297
rs367807796	in-del	-/T			intron-variant	KMT2A	GRCh38.p7	11:118481224	TGTACCCATTAACCA[-/T]CCCCACTTTCCCCCT	4297
rs367846617	snp	C/T	4.94654e-05	0.00497295	synonymous-codon, nc-transcript-variant, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519625	TCTTCTAGGTGTTAA[C/T]GGTTTGAGGATGCTG	4297
rs367851276	snp	C/T			missense	KMT2A	GRCh38.p7	11:118476917	TGTTTCCTGATGACA[C/T]GCCCACCCTGAGTGC	4297
rs367897365	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118494992	GGAGCTTGGTTTAAT[G/T]GTGACAAATGTACAA	4297
rs367939528	snp	A/T	8.23866e-05	0.00641767	missense	KMT2A	GRCh38.p7	11:118502577	AGGAATAATGTTTCC[A/T]CAGTCTCCACCACCG	4297
rs367939996	snp	G/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512801	ACACTTACCTGTTTT[G/T]TGTTTTTTTTTTTTT	4297
rs367948360	snp	A/G	0.000197801	0.00994291	intron-variant	KMT2A	GRCh38.p7	11:118480242	AGCAAGCTAAAGGTA[A/G]TGTTGTTAAAAAGGT	4297
rs367955473	in-del	-/G			intron-variant	KMT2A	GRCh38.p7	11:118471502	TTTGAGGCAAATTTT[-/G]GGTGAAAAGAAACTA	4297
rs367955871	snp	A/G	1.85407e-05	0.00304467	intron-variant	KMT2A	GRCh38.p7	11:118488800	CAGCTGGGCCTCTGT[A/G]TCAGTGGGTTCTGTA	4297
rs368088982	snp	A/T			missense	KMT2A	GRCh38.p7	11:118503685	ATCTTCCAGTACAGG[A/T]CAGAAACCTAATGCT	4297
rs368102328	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118466314	CAGCCTGAGTGACAG[A/G]GTGAGCACTGGCAAA	4297
rs368107581	snp	C/T	0.000157987	0.00888644	missense	KMT2A	GRCh38.p7	11:118436792	GCCTCGTCTTCGTCT[C/T]CGTCATCGTCCTCAG	4297
rs368226668	snp	C/G	0.000153988	0.00877328	intron-variant, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512057	TTATTCCACTCCTGT[C/G]TCAGAATATTATGGT	4297
rs368245102	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118442902	CTATCTTTTATTAAG[A/T]AAAAGGAATCTTAAG	4297
rs368263875	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118518387	TTAACAGCATGAGAC[A/G]GTGAGTAGAACAAAG	4297
rs368269082	snp	A/G	3.34364e-05	0.00408865	synonymous-codon	KMT2A	GRCh38.p7	11:118498372	TTTGGATTTTTAGAG[A/G]TGTGAATTCTGCCAA	4297
rs368395489	snp	A/C	1.65059e-05	0.00287275	synonymous-codon	KMT2A	GRCh38.p7	11:118484299	TGGAGTCCACAGGAT[A/C]AGAGTGGACTTTAAG	4297
rs368396469	snp	A/G	0.000153988	0.00877328	intron-variant	KMT2A	GRCh38.p7	11:118481692	CACTATAGACAGATG[A/G]TGTTGTTGTGTTTTT	4297
rs368484535	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118465912	GTTTTGGCTGTTTTT[C/G]TTTTGTTTTGTTTTT	4297
rs368516174	snp	C/T	3.31526e-05	0.00407127	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473175	TTCTGCATCTGGTAC[C/T]GCTGCTTCAGCCCGA	4297
rs368516469	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118443875	TATAGTGTTTTATCC[A/G]TTTTCTTGCATTTCT	4297
rs368581848	snp	A/G	0.00636936	0.0560724	intron-variant	KMT2A	GRCh38.p7	11:118477707	GAGAGGGGTTTTGCT[A/G]TGTTGGCCAGGCTGG	4297
rs368589265	snp	C/T	3.29506e-05	0.00405884	missense	KMT2A	GRCh38.p7	11:118503607	ATCCAGGAGATGGTC[C/T]AGTGGCCCAACCAAG	4297
rs368593143	snp	G/T	0.000153988	0.00877328	intron-variant	KMT2A	GRCh38.p7	11:118507620	GCAGGGTAAGCTGAA[G/T]AATTCGTCTTTTAAG	4297
rs368607157	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118514404	TTGTTCTGCAGCCAC[A/G]CTACACTATTTACTG	4297
rs368659701	snp	C/G	3.29473e-05	0.00405864	missense, intron-variant	KMT2A	GRCh38.p7	11:118472961	TTTTGCCTGCTTCCA[C/G]TGCTCCTATGCAAGG	4297
rs368664186	snp	C/G	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118489501	AATTGGGTGTAATCA[C/G]TTGCCTATTTTGTGT	4297
rs368675058	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118440552	TTCGTTTATTAATGT[C/T]ATAATCCAGTTACCT	4297
rs368715915	snp	C/G	0.000153988	0.00877328	intron-variant	KMT2A	GRCh38.p7	11:118477024	TCGGAACAGACTTTT[C/G]ATTTGTTTGTTGATT	4297
rs368730687	in-del	-/AT			intron-variant	KMT2A	GRCh38.p7	11:118502303	TCCAGTTACCTATAA[-/AT]ATATATATATATATA	4297
rs368780499	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118486428	GTACCACCTTTACAA[G/T]GAGGAAGGAAAAAGT	4297
rs368787188	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118437818	GTCCACTGTCCCCTA[A/G]GCTTAGAGAAGAGCA	4297
rs368814892	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118498317	GAGGAGACGGTAAAC[A/G]TCTTAAAACATATGA	4297
rs368824862	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118510203	ATTAGCACCATTTAG[A/G]TGGCTGTTTTATGCT	4297
rs368828398	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118456581	CTGACCTCATGATTC[A/G]CCCACCTTGGCCTCC	4297
rs368865070	snp	A/G	1.64732e-05	0.0028699	synonymous-codon	KMT2A	GRCh38.p7	11:118504667	AGAGGAACAGTTTGA[A/G]TTGCCTCTAGAGCTA	4297
rs368903972	snp	C/G	1.65869e-05	0.00287979	intron-variant	KMT2A	GRCh38.p7	11:118484852	CTAAGTGACCTTTCT[C/G]TCTCCACAGGAGGAT	4297
rs368904319	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118456126	TAGATGTGAGCCACT[A/G]CACCTGGCCTCTCCC	4297
rs368926838	snp	C/G/T	3.40234e-05	0.00412439	missense, intron-variant	KMT2A	GRCh38.p7	11:118472150	AAGCCCCAGAAAGTC[C/G/T]GGAAAGACAAGGAAG	4297
rs368932372	snp	A/T	3.31483e-05	0.004071	intron-variant	KMT2A	GRCh38.p7	11:118499786	CTCTCTCAAAAAAAT[A/T]AAATGACGCTCATAA	4297
rs368968210	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118460235	CATCCTTTGGAAGAA[C/T]TTTGAAATTTGAATA	4297
rs368968658	snp	G/T	4.06529e-05	0.0045083	intron-variant	KMT2A	GRCh38.p7	11:118491945	TAGGCCAAGTCTCAT[G/T]TTTTTCTGAGAGCTT	4297
rs368998107	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118479158	ATTATTTACTACAAT[C/T]ACCCTGTTGTGCTAT	4297
rs369080295	snp	C/T	4.94572e-05	0.00497254	synonymous-codon	KMT2A	GRCh38.p7	11:118491200	TTTGCTTTCAGGAAA[C/T]TTCTGCCCTCTCTGT	4297
rs369115378	snp	C/T	1.64944e-05	0.00287175	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521434	TAAGTCTCCCACTTG[C/T]ACTCACACAGTTCTT	4297
rs369115623	snp	A/C			upstream-variant-2KB	KMT2A	GRCh38.p7	11:118436034	CTGTTCGATTCCCAG[A/C]GCGTCCCGGGAACGT	4297
rs369139972	snp	C/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118514581	GAGTAGCTGGGACTA[C/T]AGGCGCATGCTACCA	4297
rs369165358	snp	A/G	1.67175e-05	0.0028911	intron-variant	KMT2A	GRCh38.p7	11:118491360	TTCTTTCTAGGTACT[A/G]CTACATTTATTAGCC	4297
rs369182428	snp	A/G	3.29995e-05	0.00406185	missense, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522156	GCGCCAAGAAATGCC[A/G]GAAGTTCCTAAACTA	4297
rs369226798	snp	G/T			upstream-variant-2KB, downstream-variant-500B, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118526888	AGAAAAGCGGGAGGG[G/T]CATGGCCTGTGACCT	4297
rs369292004	snp	A/G	0.000214233	0.0103475	synonymous-codon	KMT2A	GRCh38.p7	11:118506005	CTTAACCAACCCAAG[A/G]TTGCTTGGTACCCCA	4297
rs369299385	snp	A/G	1.64841e-05	0.00287085	missense	KMT2A	GRCh38.p7	11:118506156	ACCCCCTCTACTGCT[A/G]CAATAACAGCGGCAT	4297
rs369338239	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118507301	TATGTAGCCACCACT[C/G]GGATCAAGATACAGA	4297
rs369354491	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118481048	ATCACATCAGGGTAC[A/G]TGGGATGTCCATTAC	4297
rs369360540	snp	A/G	1.65844e-05	0.00287957	intron-variant	KMT2A	GRCh38.p7	11:118468734	TGTGTTTGTATGCAC[A/G]TTTTTGCTTCTGATT	4297
rs369376897	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118487519	CTCACCCAAATTCCC[G/T]AAGTGTTAATATGTT	4297
rs369386177	snp	A/C	0.0170251	0.090679	intron-variant	KMT2A	GRCh38.p7	11:118474961	ACGGTGAAACCTCAT[A/C]TCTACTAAAAAAAAA	4297
rs369443279	snp	C/T	0.000153988	0.00877328	missense	KMT2A	GRCh38.p7	11:118502596	TCTCCACCACCGGGA[C/T]CGCTACTGATCTTGA	4297
rs369519117	snp	C/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521030	CATATCCTGGGATCC[C/T]GCACCTCCTTGTGTT	4297
rs369525225	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118447092	TCCCCAGATCCTAAC[A/T]CTTCCATGAAGTTTT	4297
rs369529777	snp	C/T	0.000165229	0.00908775	synonymous-codon	KMT2A	GRCh38.p7	11:118481764	TGAAAAGAAAGACAG[C/T]AAAGAGAGCAGTGTT	4297
rs369566552	snp	G/T	3.33389e-05	0.00408269	missense, intron-variant	KMT2A	GRCh38.p7	11:118473221	CATTCTGGAACAAGG[G/T]TTGATATGCACAAAA	4297
rs369587768	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118466437	GCTGGGATTACAGGT[A/T]TGAGCTACTGTGCTG	4297
rs369637853	snp	A/C	1.64773e-05	0.00287026	missense	KMT2A	GRCh38.p7	11:118504911	ATGGATGCAGACCAC[A/C]TCTCTAGCCCTCCTT	4297
rs369646146	snp	C/G	4.94303e-05	0.00497119	missense	KMT2A	GRCh38.p7	11:118491848	CTGGCCCTTGAAAAA[C/G]AGCTGCAGATTTCTC	4297
rs369656714	snp	C/T	0.00557542	0.0525036	intron-variant	KMT2A	GRCh38.p7	11:118487916	CTGGGCGTGGTGGCT[C/T]ACGCCTATAATCCCA	4297
rs369677044	snp	C/T	0.00318978	0.0398085	intron-variant	KMT2A	GRCh38.p7	11:118497843	AATTATAGTTGCTTT[C/T]TTGAGGTTATCTTCA	4297
rs369766899	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118507672	ACCTCATTTAAAAAA[C/T]AGTTCTTCCAGGCCG	4297
rs369776198	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118471019	GGGAGTAGATTTAGT[A/G]GACACATTATGTCAC	4297
rs369782631	snp	C/G	0.000153988	0.00877328	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473568	TCCTTCTCATTCCCT[C/G]ACTCAGTCTGGGGAA	4297
rs369813563	snp	A/T			missense	KMT2A	GRCh38.p7	11:118506115	CGCCAAGTTCAGGAA[A/T]GTTTCCACAACTGGG	4297
rs369821804	snp	A/G	0.000153988	0.00877328	missense, intron-variant	KMT2A	GRCh38.p7	11:118473779	GAGAAGGACAAGAGT[A/G]GAGAGAGAGACCGGG	4297
rs369909433	snp	A/G	8.62984e-05	0.00656824	intron-variant	KMT2A	GRCh38.p7	11:118509943	ATCTATTTTCTCCCT[A/G]TTAGAACCTAAAACA	4297
rs369943312	snp	A/G	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118482277	AAAAACAGTTAAATT[A/G]GAGGTATTGTTTTAA	4297
rs369945343	snp	C/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118515586	TCCCACAATAACATT[C/T]AGTCATCACAGTGTT	4297
rs369974258	snp	A/C	3.35031e-05	0.00409273	missense	KMT2A	GRCh38.p7	11:118495881	CTGCATCCTCCTACA[A/C]CACCAATTTTGAGTA	4297
rs369982584	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118489636	AATAAATCTATCTCA[A/G]TGCTTTAATTGGGAG	4297
rs369995531	snp	A/T	0.000153988	0.00877328	missense	KMT2A	GRCh38.p7	11:118510112	ATCTGTGCAGAAAGT[A/T]TTGAAGGTGAGTGGA	4297
rs370006264	snp	C/T	9.96628e-05	0.00705843	intron-variant	KMT2A	GRCh38.p7	11:118501667	GTTTTTATTTCCTGC[C/T]ACAGAAAGTTCATCA	4297
rs370121930	snp	C/T	0.000153988	0.00877328	missense	KMT2A	GRCh38.p7	11:118501830	CCAACACAGAGATCC[C/T]CTGGCTGTCGACCGT	4297
rs370130777	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118447055	TTGGGCTTATTATTC[A/G]TCTCCCATGGTTCAA	4297
rs370177252	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118466256	CATTGCTAGAGCCCA[A/G]GAGTTTGAGGCTGCA	4297
rs370181042	snp	A/G	9.89446e-05	0.00703296	missense	KMT2A	GRCh38.p7	11:118474211	GCAGACAAGCTTCCA[A/G]TGACTGACAAGAGGG	4297
rs370196316	snp	C/T	0.000148249	0.00860829	synonymous-codon	KMT2A	GRCh38.p7	11:118505831	TGTGGGAGGAACTGC[C/T]GCCACAGCGGCAGGC	4297
rs370201364	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118464143	GGAAAAAATTCATCT[C/T]GTTCATGCCGTAATT	4297
rs370344265	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118475744	AATAAATAAATAAAA[G/T]TAATGTTATTCAACC	4297
rs370374383	snp	C/T	4.95724e-05	0.00497833	missense	KMT2A	GRCh38.p7	11:118481876	CCTCCTCCACGAAAG[C/T]CCGTCGAGGAAAAGA	4297
rs370430917	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118458797	ATTCCCAAAGGGGAA[G/T]TGGTATTCTTTTTAA	4297
rs370434090	snp	A/G	3.48699e-05	0.00417537	intron-variant	KMT2A	GRCh38.p7	11:118495944	CTCTAGATGCAGATG[A/G]TTGACTTCGTGAATC	4297
rs370435161	snp	C/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118516101	CTTGTGTTCCCCAGT[C/G]CAAAACCTGTCCATT	4297
rs370448160	snp	A/G	5.69028e-05	0.00533368	intron-variant	KMT2A	GRCh38.p7	11:118482382	AGTACTAAAGTAGTC[A/G]TTGCCAGCATCTGAC	4297
rs370487885	snp	A/G	0.000304646	0.0123382	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520921	AGAATTACAGAAAAC[A/G]AATGCAGTTTTTCAA	4297
rs370519458	snp	C/T	0.000197664	0.00993947	synonymous-codon	KMT2A	GRCh38.p7	11:118506365	TACCCAGACGGTAGA[C/T]GCTCCTAATAGCATG	4297
rs370542169	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118485810	GCATATAGCTGGGCA[C/T]GGTGGCTCACGCCTG	4297
rs370652587	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118456124	TATAGATGTGAGCCA[C/T]TGCACCTGGCCTCTC	4297
rs370698782	snp	C/T	3.46164e-05	0.00416017	missense	KMT2A	GRCh38.p7	11:118506625	CAGACCAAGAAACGA[C/T]ATCCCTGACCTCAGG	4297
rs370731183	snp	A/G	1.65302e-05	0.00287486	missense	KMT2A	GRCh38.p7	11:118481918	AATGTCTCGGCCCCT[A/G]GGCCTGAATCCAAAC	4297
rs370745462	snp	A/G/T	3.29501e-05	0.00405884	missense	KMT2A	GRCh38.p7	11:118503408	CCCAAAGCTCCACCC[A/G/T]TGCAAGTAGAAGGAT	4297
rs370764446	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118451265	CACCCAGGCTGGGAT[A/G]CAGTGGCACAAACAC	4297
rs370779303	snp	C/T	1.67699e-05	0.00289563	intron-variant	KMT2A	GRCh38.p7	11:118507519	AAAGATACAAATGCC[C/T]GTGTTCCAGGACTCC	4297
rs370781768	snp	A/C/T	0.000100638	0.00709301	synonymous-codon	KMT2A	GRCh38.p7	11:118509142	TTTATTTAGGCAAGT[A/C/T]GCTGTTCTTCCGGAA	4297
rs370793886	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118491417	TGGTTGTGTTGTTAT[A/T]TGAAATCTCTAAATT	4297
rs370795871	snp	C/T			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118524074	AAGTTGAATGGCAAC[C/T]TGACATTTTTGCATC	4297
rs370812470	snp	G/T	1.65135e-05	0.00287341	missense	KMT2A	GRCh38.p7	11:118503096	GATGAAGATACTGAA[G/T]TCAAAACCTTGAAGC	4297
rs370854390	snp	C/T	0.000153988	0.00877328	missense, intron-variant	KMT2A	GRCh38.p7	11:118472930	ATGCCTCCAACAATC[C/T]CCTTAGCATCACCAT	4297
rs370899148	snp	A/G	3.29815e-05	0.00406075	missense	KMT2A	GRCh38.p7	11:118502482	GCATTGGCTCCAGGC[A/G]TCACAGTACCTCTTC	4297
rs370949437	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118475723	GCGAGACTCCGTCTC[C/T]AAAAAAATAAATAAA	4297
rs371059297	snp	A/C/G	8.25438e-05	0.00642389	intron-variant, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512060	TTCCACTCCTGTCTC[A/C/G]GAATATTATGGTAAA	4297
rs371070385	snp	C/T	1.64749e-05	0.00287005	synonymous-codon	KMT2A	GRCh38.p7	11:118499386	AAGGAAGTTTCTCAA[C/T]GGCTTGGAACCAGAA	4297
rs371190424	snp	A/C			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118518781	AGTTAGAGTCTGTCT[A/C]AAAAAAAAAAAAAAA	4297
rs371238665	snp	A/G	0.000184575	0.00960485	intron-variant	KMT2A	GRCh38.p7	11:118476781	TGTATGGTTGTTATT[A/G]TTTTTGGATTGCCTC	4297
rs371281004	snp	G/T	1.6492e-05	0.00287154	synonymous-codon	KMT2A	GRCh38.p7	11:118506128	AATGTTTCCACAACT[G/T]GGGACATCACAGACC	4297
rs371289157	snp	C/T	0.000153988	0.00877328	synonymous-codon, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519763	CCCCTTGAACCCTCA[C/T]GGCTCAGCCAGGGCT	4297
rs371299248	snp	A/G	0.000153988	0.00877328	synonymous-codon	KMT2A	GRCh38.p7	11:118491251	TGACTATGAGAGTAA[A/G]ATGATGCAATGTGGA	4297
rs371302797	snp	C/T	1.68741e-05	0.00290461	intron-variant, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118511932	TTCTGGCTTACGGGT[C/T]TTCTTTATTTCCTTT	4297
rs371343232	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118437590	CCCGCCCTACCCCAC[C/T]GGGGAAAATCTCTCC	4297
rs371376109	snp	C/T	0.000153988	0.00877328	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473178	TGCATCTGGTACCGC[C/T]GCTTCAGCCCGATTG	4297
rs371413016	snp	C/T	4.94548e-05	0.00497242	synonymous-codon	KMT2A	GRCh38.p7	11:118498071	ATCAGGGGCAAGCAG[C/T]TGGTAAGACCTTATG	4297
rs371553631	snp	A/G/T	8.23749e-05	0.00641728	synonymous-codon	KMT2A	GRCh38.p7	11:118505477	GGTTCAGCCTCCTCC[A/G/T]GATCCCCAACTTTTG	4297
rs371576161	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118487590	CATATACACATTTTA[A/C]CTGTAGATACACATG	4297
rs371588017	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118446710	TTGTGGTAATCTTCT[C/T]ATTGGTCTTCCCACC	4297
rs371635542	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118466930	CAGGCATAGTGGTGC[A/C]TGTATGTAGTCCGAG	4297
rs371669527	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118479556	TGGTTTGGTCTGACC[C/T]TAAACAAGAATCTTG	4297
rs371770346	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118456625	TTACAGGCATGAGCC[A/G]CCGCGCCTGGCATGC	4297
rs371772102	snp	A/T	0.000197707	0.00994053	missense	KMT2A	GRCh38.p7	11:118502539	GGATAATGTCTCCAA[A/T]GAGAACTGGGAATAC	4297
rs371789726	snp	A/C/G	4.97088e-05	0.00498517	intron-variant	KMT2A	GRCh38.p7	11:118499794	AAAAAATAAAATGAC[A/C/G]CTCATAATCTTCTCT	4297
rs371822279	snp	C/T	3.30704e-05	0.00406622	intron-variant	KMT2A	GRCh38.p7	11:118496408	TAGTTAATACATACT[C/T]CAAAAGAACTGTTTG	4297
rs371836362	snp	C/T	0.00159617	0.0282053	intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118518950	CAGGCGTGGTGGCGG[C/T]GCCCGTAGTCCCAGC	4297
rs371837293	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118437168	GGGCGTTTGCCCCCC[C/G]CTCTCCTCCCCCTGA	4297
rs371867946	snp	A/G	4.94181e-05	0.00497057	synonymous-codon	KMT2A	GRCh38.p7	11:118505822	ACCACAGAGTGTGGG[A/G]GGAACTGCTGCCACA	4297
rs372015978	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118477369	GTTCTTAAGTGCAGA[G/T]TAGCCACTCAGAACA	4297
rs372071770	snp	A/C	0.000153988	0.00877328	missense	KMT2A	GRCh38.p7	11:118490158	TGTTCGCTGTAAGAG[A/C]TGTGGATCCACAACT	4297
rs372125752	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118474601	ATCTGTGGAAAACTG[A/G]TGAACTAAGGCTGAA	4297
rs372133306	snp	A/G	1.64779e-05	0.00287031	synonymous-codon	KMT2A	GRCh38.p7	11:118503716	TCCAGATGGCCCCAA[A/G]CCTCAGGAGGATGGC	4297
rs372145951	snp	A/G	1.69893e-05	0.00291451	intron-variant	KMT2A	GRCh38.p7	11:118507626	TAAGCTGAAGAATTC[A/G]TCTTTTAAGACTAAG	4297
rs372168235	snp	A/G	0.000153988	0.00877328	intron-variant	KMT2A	GRCh38.p7	11:118484144	TGTGAAGGCAAATAG[A/G]GTGTGATTTTGTTCT	4297
rs372208886	snp	A/G	4.94491e-05	0.00497213	synonymous-codon	KMT2A	GRCh38.p7	11:118504364	CGACAAAAATTTACT[A/G]GACACCTATAATACT	4297
rs372232178	snp	C/T	1.64966e-05	0.00287194	missense, intron-variant	KMT2A	GRCh38.p7	11:118473522	CTGTTAGTCCTCTTG[C/T]CACTAGTGCCTTAAA	4297
rs372236307	snp	G/T	0.0023933	0.0345097	intron-variant	KMT2A	GRCh38.p7	11:118456416	TGACCTTGGTTTACT[G/T]CAACCTCCGCCTCCT	4297
rs372259453	in-del	-/C			intron-variant	KMT2A	GRCh38.p7	11:118482752	CTGTCTTTATTTAAA[-/C]AAAAAAAAAAAAAAG	4297
rs372354558	snp	C/T	1.65206e-05	0.00287403	synonymous-codon	KMT2A	GRCh38.p7	11:118504169	GAACTTAAAGATTGA[C/T]AGACCTGAAGATGCT	4297
rs372359068	in-del	-/T			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522863	GACAGTAGGAGCGGC[-/T]TTCCCTCTCCCATTC	4297
rs372396978	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118438287	TCCCCATTAGTACTG[A/G]GGCAAGAACGGAGTT	4297
rs372465982	snp	C/G/T	3.29762e-05	0.00406045	intron-variant	KMT2A	GRCh38.p7	11:118480255	TAGTGTTGTTAAAAA[C/G/T]GTCTTCCCCCAAATG	4297
rs372478830	snp	A/T	0.000153988	0.00877328	missense	KMT2A	GRCh38.p7	11:118505941	ATGTTGTATCCATGC[A/T]AACTACCACAACCCC	4297
rs372482881	snp	A/C/G	4.95342e-05	0.00497645	intron-variant	KMT2A	GRCh38.p7	11:118499926	TCAGTAAGTAGCACT[A/C/G]TAAAGAGAAGAGAGC	4297
rs372495758	snp	A/G	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118459906	CTCTGGTCATGTCAG[A/G]ATGGTCTCAAACTCC	4297
rs372502484	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118513249	ACTTTGTCACAAAAA[A/G]AAGAAGAAGAAGAAG	4297
rs372503677	snp	A/G	1.66468e-05	0.00288498	intron-variant	KMT2A	GRCh38.p7	11:118489778	TATCTTTTTGCCATT[A/G]TATTTTCTTACAGCA	4297
rs372553474	snp	A/G	1.67038e-05	0.00288992	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520756	TTCAAGACTCAAAAC[A/G]TTATTTCCTGAAAAA	4297
rs372658892	snp	A/C			upstream-variant-2KB	KMT2A	GRCh38.p7	11:118435433	TCATAATGCCCAACG[A/C]TCTCCTCCTCCCCCT	4297
rs372664716	snp	C/T			missense	KMT2A	GRCh38.p7	11:118490204	GATGCACAGTGGTCT[C/T]ATGATTTCTCACTGT	4297
rs372686008	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118494439	TTTAATGCTTACCTA[C/T]AAGTAATTACCCTGT	4297
rs372694407	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118514494	CACCCAGGCTGGAGT[A/G]CAGTGGCGTGATCTC	4297
rs372697144	snp	A/G	0.0023933	0.0345097	intron-variant	KMT2A	GRCh38.p7	11:118478482	GCAGCCATTAGCCAC[A/G]TGTGGCTATTGAGCG	4297
rs372708660	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118518804	AAAAAAAAGCCGGGC[A/G]CGGTGGCTCACACCT	4297
rs372739146	snp	C/T	8.27904e-05	0.00643338	intron-variant	KMT2A	GRCh38.p7	11:118500979	TTTTCCCAAATCTGT[C/T]TACCCAGGTGTTCCA	4297
rs372755187	snp	A/T	0.000153988	0.00877328	synonymous-codon	KMT2A	GRCh38.p7	11:118503113	CAAAACCTTGAAGCT[A/T]TCTGGAATGAGCAAC	4297
rs372761509	in-del	-/A			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520650	GCGAAACTCCATCTC[-/A]AAAAAAAAAAGGGGG	4297
rs372770910	in-del	-/A/AA	0.477853	0.102875	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118518781	GTTAGAGTCTGTCTC[-/A/AA]AAAAAAAAAAAAAAA	4297
rs372782628	snp	C/T	0.000214817	0.0103616	synonymous-codon	KMT2A	GRCh38.p7	11:118481878	TCCTCCACGAAAGCC[C/T]GTCGAGGAAAAGAGT	4297
rs372784331	snp	C/G/T	4.95081e-05	0.00497514	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521450	ACTCACACAGTTCTT[C/G/T]TGTTTTGCTGTAGAA	4297
rs372798047	snp	A/G	0.000313622	0.0125185	intron-variant	KMT2A	GRCh38.p7	11:118468854	CTTCAGGTACGGCCA[A/G]TTAAGTGCATGGTGC	4297
rs372849484	snp	A/G			synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473352	ATCTTCTTCAGGAGT[A/G]TCCAATAGAAAAAGG	4297
rs372966870	snp	C/T	0.000153988	0.00877328	intron-variant	KMT2A	GRCh38.p7	11:118485026	CATAAATTATTTTTC[C/T]GTGGATGAAATTACT	4297
rs372974093	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118518652	GCTGGGCATGGTGAC[A/G]TGCCCCTGTAGTCCC	4297
rs372983967	snp	A/G	0.00358779	0.0422022	intron-variant	KMT2A	GRCh38.p7	11:118486653	TGACGCAGGAGGACC[A/G]CTTGAGCTCAGGAGT	4297
rs372992626	snp	C/G	6.59337e-05	0.0057413	intron-variant	KMT2A	GRCh38.p7	11:118488589	TTATTTGACATACTT[C/G]TATCTTCCCATGTTC	4297
rs372995209	snp	A/G	1.67287e-05	0.00289207	missense	KMT2A	GRCh38.p7	11:118501854	CGACCGTTGCCTTCT[A/G]CAGGTAAAAGACTTT	4297
rs373014626	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118447173	GTGTTTTGTATGTTA[A/T]CCTTAAAAAATTTAA	4297
rs373020975	snp	A/G	1.64811e-05	0.00287059	synonymous-codon	KMT2A	GRCh38.p7	11:118503020	ACACCTCCATTTGAG[A/G]GGGCAAAGGAATGAT	4297
rs373064982	snp	C/G	0.000153988	0.00877328	missense	KMT2A	GRCh38.p7	11:118504969	ACAATCAGGATTTAA[C/G]TAGGAACAGTAGCAC	4297
rs373098708	snp	A/G	1.64849e-05	0.00287092	synonymous-codon	KMT2A	GRCh38.p7	11:118510024	GCAAGAACAAAAGCG[A/G]AAGGAAAGCATTACT	4297
rs373111056	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118500880	ATAAAGCTAAACTCT[C/G]TAATTAAGAGGGCCA	4297
rs373125614	snp	C/T	1.64746e-05	0.00287002	synonymous-codon	KMT2A	GRCh38.p7	11:118506395	GGGACTGGAGCAGAA[C/T]AAGGCTTTATCCTCA	4297
rs373127478	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118450427	CATCTTTGCTGCTTA[C/T]TCTTGTTGACATGGA	4297
rs373156033	snp	A/G			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118523155	TGTAGGAGAGGAAAA[A/G]GATTATTTAAATAGG	4297
rs373165991	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118497212	TTTCTCCATGTTGGT[A/C]AGGCTGGTCTCAAAC	4297
rs373188614	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118511064	GTTTTAGAGGGCTTT[C/T]AGTGCCAAACCTTGA	4297
rs373195384	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118482217	TTCAAGAAAATCAGC[G/T]CTCTTTCTAACTATT	4297
rs373199348	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118438504	GGGGCTGAAGCGAAG[C/G]GGGGTAGGGGGTTGC	4297
rs373277063	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118475097	GAGATCCCGCCACTG[C/T]ACTCCAGCCTGGGCC	4297
rs373329927	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118455244	TGTCTCTCCATTAGA[C/T]TGTAGCTTCATGGGG	4297
rs373330424	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118507727	CCTAGTAGTCTGGGA[C/G]GCCGAGGCAGGTGGA	4297
rs373345566	snp	G/T	9.88843e-05	0.00703081	missense	KMT2A	GRCh38.p7	11:118506180	GCGGCATCTAGCATC[G/T]GTGTGCTCCCCTCCA	4297
rs373383201	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118460683	TTTTTTTAGAGACAG[G/T]ATCTGGCTATGTTGC	4297
rs373406129	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118482325	AGAGTTTAAATAGTT[G/T]TTTTTTTTTTTTTCT	4297
rs373435126	snp	C/G/T	0.000365794	0.0135193	missense	KMT2A	GRCh38.p7	11:118491896	GCTTTGTTGAATTCT[C/G/T]GGACTACCAGCCATT	4297
rs373457908	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118490091	TAAAGATATTAAAAA[C/T]AAGAAATTCCTATTG	4297
rs373487642	snp	A/G	0.000153988	0.00877328	synonymous-codon	KMT2A	GRCh38.p7	11:118504769	TATCTCAGACTCAGG[A/G]GAGAAGAGAGTAACC	4297
rs373574814	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118444045	TCATTCTTATTTTAC[A/G]GCATCAAGGTAATGG	4297
rs373584515	snp	C/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118517121	AGTTTGCCAGCTGGG[C/T]GCGGTGGCTCACGCC	4297
rs373610224	snp	C/T	3.32027e-05	0.00407434	intron-variant	KMT2A	GRCh38.p7	11:118482508	AAGGTGAGGAGAGAT[C/T]TGTTTCTCTGCCATT	4297
rs373625999	snp	A/G	3.30786e-05	0.00406672	synonymous-codon	KMT2A	GRCh38.p7	11:118503191	GAGACAGAAAGGGAA[A/G]AAATCCTGTAAAGAA	4297
rs373716647	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118463814	CAGAATTTCAAAATT[G/T]TGTATGCACCAAAAT	4297
rs373756201	snp	C/T			utr-variant-3-prime, intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118525046	GCCAAATTTTCAGCA[C/T]ACCTGCCAGCAACTT	4297
rs373803711	snp	A/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520161	TGCATCAGAATTTCC[A/T]GGATAAGATTTAAAA	4297
rs373805126	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118510711	CTTATTCATCTTTGT[A/G]TCGCAAGCATCTAAG	4297
rs373837159	snp	C/T	0.0023933	0.0345097	intron-variant	KMT2A	GRCh38.p7	11:118493634	TGCCTGTTAATTTTA[C/T]GATTTTAAGTATGTA	4297
rs373950413	snp	A/G	0.000104592	0.00723083	intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118511908	TTAAGAAGGGTTTAC[A/G]TGCATATTTTCTGGC	4297
rs374005016	snp	C/T	0.000153988	0.00877328	missense, intron-variant	KMT2A	GRCh38.p7	11:118473585	CTCAGTCTGGGGAAT[C/T]TGCAGAGAAAAATCA	4297
rs374068637	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118508399	TAATGAGTCCTCTAT[G/T]GATATACATTTGGAT	4297
rs374085090	snp	C/T	4.95618e-05	0.00497779	missense, intron-variant	KMT2A	GRCh38.p7	11:118472478	ACCCTCCAATTAAAA[C/T]TGCCCGATTAGAGTC	4297
rs374176458	in-del	-/C			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118515666	ATTTGGTACCATGTC[-/C]ATTTCTTTTTCTGTC	4297
rs374178581	snp	G/T	0.000153988	0.00877327	intron-variant	KMT2A	GRCh38.p7	11:118481688	TTCTCACTATAGACA[G/T]ATGATGTTGTTGTGT	4297
rs374190903	snp	C/T	1.6473e-05	0.00286988	synonymous-codon	KMT2A	GRCh38.p7	11:118476915	TGTGTTTCCTGATGA[C/T]ATGCCCACCCTGAGT	4297
rs374209348	snp	A/C/G	1.7626e-05	0.00296861	intron-variant	KMT2A	GRCh38.p7	11:118490254	CTTTGCTAAAGGTAC[A/C/G]CAAAAAAGCCAGTTT	4297
rs374335124	snp	A/G	3.38158e-05	0.00411178	intron-variant	KMT2A	GRCh38.p7	11:118510125	GTATTGAAGGTGAGT[A/G]GATTAAATCAGGTTG	4297
rs374337395	snp	A/G	0.000115495	0.00759831	synonymous-codon	KMT2A	GRCh38.p7	11:118501694	ATCAAAAGAGAGTCA[A/G]AACACAGCTGAAATT	4297
rs374337880	snp	C/G	1.64947e-05	0.00287177	intron-variant, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512036	TGCAGGTAATGGCTG[C/G]AGGTGTTATTCCACT	4297
rs374385218	snp	G/T	1.64822e-05	0.00287068	missense, intron-variant	KMT2A	GRCh38.p7	11:118474011	CTTCTGTGACTCTTG[G/T]GGATACAACAGCTGT	4297
rs374420996	snp	A/C	3.29511e-05	0.00405887	missense	KMT2A	GRCh38.p7	11:118503664	CTCAAAGTAACAACT[A/C]TCAGAATCTTCCAGT	4297
rs374437257	snp	G/T	1.69238e-05	0.00290888	intron-variant	KMT2A	GRCh38.p7	11:118501181	TGGGACTTGAGGCTG[G/T]GCACAGTGGCTCACG	4297
rs374441662	snp	C/T	0.000153988	0.00877328	intron-variant, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519575	CCATGCTGTTTCCTG[C/T]TGACTGCGCTCCTCA	4297
rs374441915	snp	C/T	1.64741e-05	0.00286998	missense	KMT2A	GRCh38.p7	11:118505539	GTACCACAGTAGCCA[C/T]TCCATCCTCTGGACT	4297
rs374454716	snp	A/C	0.000153988	0.00877328	synonymous-codon	KMT2A	GRCh38.p7	11:118499389	GAAGTTTCTCAATGG[A/C]TTGGAACCAGAAAAT	4297
rs374464983	in-del	-/TT			intron-variant	KMT2A	GRCh38.p7	11:118470896	AAATTGGCAAATTCC[-/TT]TTATTTAGAATAGAA	4297
rs374476166	snp	C/G	1.65209e-05	0.00287405	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519805	CAGGCAAGTTCCCTT[C/G]TTTTCTGTCAGCAGT	4297
rs374476571	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118456424	GTTTACTGCAACCTC[A/C]GCCTCCTGGGCTCAA	4297
rs374481108	snp	C/T	0.000153988	0.00877328	synonymous-codon	KMT2A	GRCh38.p7	11:118502697	TCCACCTCTTCAAAT[C/T]TGCAAAGGACAGTGG	4297
rs374491736	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118467444	TTTCAGCCTTTTCTT[A/C]AATAGTCCAATACTT	4297
rs374507145	snp	C/G	0.000153988	0.00877328	intron-variant	KMT2A	GRCh38.p7	11:118478220	AGTGGGTGTTTCACT[C/G]TGAGATGTTGACCTC	4297
rs374534268	snp	A/G	0.00795532	0.062565	intron-variant	KMT2A	GRCh38.p7	11:118465521	GATTTCACATAAATT[A/G]TTTATTCCTTACAGT	4297
rs374545538	snp	C/G	3.3066e-05	0.00406595	missense, intron-variant	KMT2A	GRCh38.p7	11:118473134	CCTCCACTAACTCCC[C/G]AGGACGTTGGCTTTG	4297
rs374588598	snp	G/T	3.29468e-05	0.00405861	missense	KMT2A	GRCh38.p7	11:118496286	GAGTCGAGAAGACAG[G/T]CCAGAGCTGAACCCA	4297
rs374612428	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118486805	AGGTGAGAGGATCAC[C/T]TGAGCCCAGGAGATC	4297
rs374626588	snp	A/C	3.29587e-05	0.00405934	missense	KMT2A	GRCh38.p7	11:118503558	TTGCAAATAGAGTCA[A/C]CATCTCCCACAGAAC	4297
rs374632181	snp	A/G	4.95389e-05	0.00497664	missense	KMT2A	GRCh38.p7	11:118481780	AAAGAGAGCAGTGTT[A/G]TGAAGAACGTGGTGG	4297
rs374716873	snp	C/G	9.92326e-05	0.00704318	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118472668	ACTTCCTGAGGAGCG[C/G]AGCGATACCCCTGAA	4297
rs374776027	snp	C/T	1.70319e-05	0.00291816	intron-variant	KMT2A	GRCh38.p7	11:118509131	TACATTTGGTTTTTA[C/T]TTAGGCAAGTCGCTG	4297
rs374786136	snp	A/C	3.29826e-05	0.00406082	intron-variant	KMT2A	GRCh38.p7	11:118498080	AAGCAGCTGGTAAGA[A/C]CTTATGGGTAAATTT	4297
rs374789593	snp	C/T	9.89283e-05	0.00703238	intron-variant	KMT2A	GRCh38.p7	11:118496235	CTGGATCTCAAGGTA[C/T]TGATGGGAGTCTTTT	4297
rs374953594	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118494579	GAGTGGATGGATCTT[C/T]CTCTTGGTGGCCTGA	4297
rs374983006	snp	A/C	1.66888e-05	0.00288862	missense	KMT2A	GRCh38.p7	11:118474300	TCTTAAACAAACCGA[A/C]CAGCCCAAAGCACAG	4297
rs375010813	snp	C/T	9.89136e-05	0.00703186	synonymous-codon	KMT2A	GRCh38.p7	11:118506149	ATCACAGACCCCCTC[C/T]ACTGCTGCAATAACA	4297
rs375047310	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118435464	CTCTTAATCAGAAAC[A/G]TGCTCGCGAGCCCCC	4297
rs375049498	snp	C/T	0.000153988	0.00877328	missense	KMT2A	GRCh38.p7	11:118504035	GAACAGTGTGATCTT[C/T]CAAAAATCTCACAGT	4297
rs375077411	snp	A/G	3.63286e-05	0.00426181	intron-variant	KMT2A	GRCh38.p7	11:118506682	CTAGGCTGGGTCTGT[A/G]GGATTTCATGTTGTA	4297
rs375079278	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118449750	TTTAGAAAGAAGGAA[-/A]GTTGTGGATTCCTCA	4297
rs375125520	in-del	-/GA			intron-variant	KMT2A	GRCh38.p7	11:118509344	TTGGCCCACATTGGA[-/GA]CTGAAACTTGGCGCA	4297
rs375139717	in-del	-/A			intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118511896	CATCATTGGTATTAA[-/A]GAAGGGTTTACGTGC	4297
rs375240261	snp	C/T	0.000131933	0.00812089	missense, intron-variant	KMT2A	GRCh38.p7	11:118473560	TTTACTTTTCCTTCT[C/T]ATTCCCTGACTCAGT	4297
rs375244485	snp	A/G	3.59725e-05	0.00424087	intron-variant	KMT2A	GRCh38.p7	11:118509245	GAGAATATCAATGCT[A/G]AAAGGATTATGAGAA	4297
rs375252378	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520942	AGTTTTTCAAAATCA[A/G]AGCAGACCAAATGCT	4297
rs375252630	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118487988	GATTGAGACCATCCT[C/T]GCTAACACAGTGAAA	4297
rs375261287	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118446858	AGATTCTCAGCGCTG[C/T]ATGATCTTGCTAGCC	4297
rs375274654	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118437775	TCCTTTAGAATGAAG[A/G]ATTAGTGGCATCTTG	4297
rs375281059	snp	C/G	4.95054e-05	0.00497496	synonymous-codon, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522157	CGCCAAGAAATGCCG[C/G]AAGTTCCTAAACTAA	4297
rs375284231	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118489293	TATATGCAAATGCTG[C/T]ACCATTTTGTCTAGG	4297
rs375292090	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118480447	TTCCATAATAAATTT[C/T]TTAAATTTATATAAA	4297
rs375294084	in-del	-/G			intron-variant	KMT2A	GRCh38.p7	11:118446245	CCCAGCTACTTGGGG[-/G]GGCTGAGGCATGAGA	4297
rs375370470	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118502252	GTGAGACACTGTCTC[-/A]AAAAAAGTAATAATA	4297
rs375382456	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118509923	CATTTGTTACTGCAA[C/T]CACTATCTATTTTCT	4297
rs375402329	in-del	-/C			intron-variant	KMT2A	GRCh38.p7	11:118437675	ATACAGCAGTCTCTT[-/C]CCCCCCCCCGCCCCG	4297
rs375432648	snp	A/G	0.000153988	0.00877328	intron-variant	KMT2A	GRCh38.p7	11:118488798	TACAGCTGGGCCTCT[A/G]TATCAGTGGGTTCTG	4297
rs375458433	in-del	-/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118516265	GTTGGTGACAGGAAA[-/T]CTGGAATCTCTTGAT	4297
rs375465696	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118459942	TCAAGTGATCTGCCT[A/G]CCTTGGCCTCCCAAA	4297
rs375471954	snp	C/T	1.64762e-05	0.00287016	synonymous-codon	KMT2A	GRCh38.p7	11:118488700	GGACCAGCTGGAAAA[C/T]TGGTGTTGTCGTCGT	4297
rs375482063	in-del	-/T	0.0174175	0.0916809	intron-variant	KMT2A	GRCh38.p7	11:118459072	TGATTTTTCAAACTC[-/T]TTTTTTTCCCCCCTT	4297
rs375503116	snp	A/G	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118443298	TTGGACTGAGGGAAT[A/G]ACTTCCCATAAAATG	4297
rs375510527	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118477539	TTGAGACGGAGCCTC[A/T]TTGTGTTGCCCAAGC	4297
rs375512905	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118501881	CTTTATTGACCTACT[C/T]GACCTAAGAAGATCA	4297
rs375529564	snp	C/T	1.90235e-05	0.00308406	intron-variant	KMT2A	GRCh38.p7	11:118482381	CAGTACTAAAGTAGT[C/T]GTTGCCAGCATCTGA	4297
rs375533652	snp	A/G	6.76899e-05	0.00581725	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118472011	TCCTCTCAAGTCTAA[A/G]TTTAAGACAGGGAAG	4297
rs375617107	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118509372	GCACCTGTCTCTCGG[A/T]GCAGTGTTCTTCCAG	4297
rs375636934	snp	G/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118438323	TATAAACATTATTCG[G/T]CCCCCTTCAGCAAAA	4297
rs375644428	snp	A/G			missense	KMT2A	GRCh38.p7	11:118504350	ACAAGTACCCCCTCC[A/G]ACAAAAATTTACTGG	4297
rs375654135	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118511378	GCATGGAGAACAAAG[G/T]AGATAAGTAAGGAGT	4297
rs375734242	snp	C/T	1.64735e-05	0.00286993	missense	KMT2A	GRCh38.p7	11:118505947	TATCCATGCAAACTA[C/T]CACAACCCCTACAAG	4297
rs375780849	in-del	-/A	0.0689305	0.172377	intron-variant	KMT2A	GRCh38.p7	11:118485927	CTCTATTAAAAATAC[-/A]AAAAAATTAGCCGGG	4297
rs375815017	snp	A/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118517688	CCACAAGAAATTTAA[A/T]AATTAGCCAAACACA	4297
rs375826193	snp	C/T	1.64882e-05	0.00287121	intron-variant	KMT2A	GRCh38.p7	11:118488568	TTGATTATGTTTTTC[C/T]ACATATTATTTGACA	4297
rs375849517	snp	C/T	6.60349e-05	0.0057457	synonymous-codon	KMT2A	GRCh38.p7	11:118481788	CAGTGTTGTGAAGAA[C/T]GTGGTGGACTCTAGT	4297
rs375852658	snp	A/G	4.94303e-05	0.00497119	missense	KMT2A	GRCh38.p7	11:118505985	TCAGTTCCAGGACAC[A/G]TCACCTTAACCAACC	4297
rs375901478	in-del	-/T			intron-variant	KMT2A	GRCh38.p7	11:118459079	TCAAACTCTTTTTTT[-/T]CCCCCCTTTGAGACA	4297
rs375905420	in-del	-/C			intron-variant	KMT2A	GRCh38.p7	11:118482339	TTTTTTTTTTTTTTT[-/C]TAATGGCCCTTTCTT	4297
rs375934901	snp	C/G			missense, intron-variant	KMT2A	GRCh38.p7	11:118474100	CTCGGCCCAACTGCC[C/G]CATCCCTGGAGAAGG	4297
rs375952502	snp	C/T	1.648e-05	0.0028705	synonymous-codon	KMT2A	GRCh38.p7	11:118504865	AACTCCTGAAGGCCA[C/T]ATGACTCCTGATCAT	4297
rs376123888	in-del	-/C	0.00318978	0.0398085	intron-variant	KMT2A	GRCh38.p7	11:118487199	ATACAGTGCTTTGCA[-/C]CCCATATATATGCCA	4297
rs376129606	snp	G/T			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118523811	GTGTAGCTTGTTTGT[G/T]CCCTGTTGACATAAA	4297
rs376136270	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118437304	CCTCCCTCCCTCCTA[A/G]AGACCTGATCCCGCC	4297
rs376154793	snp	C/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118514736	CCTCCCGAATTCAAG[C/T]GATTCTCCTGCCTCA	4297
rs376161579	snp	A/C/T	4.94298e-05	0.0049712	missense	KMT2A	GRCh38.p7	11:118505109	CAGACCACTCCACCC[A/C/T]ACCTGAAGCCAGCCA	4297
rs376170743	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118515583	AGTTCCCACAATAAC[A/G]TTCAGTCATCACAGT	4297
rs376174646	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118482222	GAAAATCAGCTCTCT[G/T]TCTAACTATTATGTT	4297
rs376179724	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118439569	TAATCAGGGGCTAAA[C/T]GTTTTCTTATCTACT	4297
rs376208372	in-del	-/T	0	0	intron-variant	KMT2A	GRCh38.p7	11:118486387	TGGTTTTTTTTTTTT[-/T]AATCTTTCTGAGTTT	4297
rs376213306	snp	C/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118469530	TATCTAGAATATCTT[C/G]AAATTCTAGACTTAC	4297
rs376303494	snp	A/G	8.26276e-05	0.00642705	missense	KMT2A	GRCh38.p7	11:118481879	CCTCCACGAAAGCCC[A/G]TCGAGGAAAAGAGTG	4297
rs376354703	snp	A/C	0.000153988	0.00877328	intron-variant	KMT2A	GRCh38.p7	11:118474319	CCCAAAGCACAGGTA[A/C]TCTTTTCCACCTTGC	4297
rs376463533	snp	A/G	1.69243e-05	0.00290893	intron-variant, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118511930	TTTTCTGGCTTACGG[A/G]TTTTCTTTATTTCCT	4297
rs376527206	snp	A/G	3.2956e-05	0.00405918	synonymous-codon, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522127	TGCCAGCAACAAGCT[A/G]CCCTGCAACTGTGGC	4297
rs376531474	snp	C/G	1.64765e-05	0.00287019	synonymous-codon	KMT2A	GRCh38.p7	11:118502588	TTCCTCAGTCTCCAC[C/G]ACCGGGACCGCTACT	4297
rs376575596	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118467372	ACAGAGCAAGACTCC[A/G]TCTCAAAAAAAAAAA	4297
rs376575957	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118445652	TTGAGCAGAATGGTC[A/C]AAAGCAGATTAGAGT	4297
rs376579850	snp	A/G	1.64857e-05	0.00287099	missense	KMT2A	GRCh38.p7	11:118503039	CAAAGGAATGATCGA[A/G]ACCAACACACAGATT	4297
rs376588074	snp	C/T	1.65765e-05	0.00287888	intron-variant	KMT2A	GRCh38.p7	11:118499962	CACAACCTGAACACA[C/T]TGAAGCCATGTGCAG	4297
rs376682610	snp	A/G	0.00478085	0.0486577	intron-variant	KMT2A	GRCh38.p7	11:118462764	AGACAGGGTTTCACC[A/G]TGTTAGCCAGGATGG	4297
rs376683569	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118445342	AACACAGTGCCTCCA[A/T]GAGTTGCTAATTATC	4297
rs376694691	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118501485	AGAAAAAAAAAAAAA[-/A]GATGTGATGGAACTT	4297
rs376704082	snp	C/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118514702	GCAATGGCGCAATCT[C/G]GGTTCACCGCAACCT	4297
rs376755301	snp	C/T	0.000307953	0.0124049	intron-variant	KMT2A	GRCh38.p7	11:118484827	AAAGTTGTGTAATTG[C/T]AAAACTTTCCTAAGT	4297
rs376775659	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118447803	AGGAATGGTAACCAG[C/T]GGTTTCCCAGCTCCA	4297
rs376776245	snp	C/T	3.29484e-05	0.00405871	missense	KMT2A	GRCh38.p7	11:118491812	GTGAACTGTACTGAG[C/T]GGCACCCTGCAGAGT	4297
rs376817515	snp	C/T	1.64808e-05	0.00287057	synonymous-codon	KMT2A	GRCh38.p7	11:118484248	CCTCAGCACTCTCTC[C/T]AATGGCAATAGTTCT	4297
rs376833433	in-del	-/CAGT			intron-variant	KMT2A	GRCh38.p7	11:118455348	TGAATGATTGAGTGA[-/CAGT]CATATTTGAATTATG	4297
rs376842254	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118507918	CAGTGAGCTGAGATC[A/G]CGCCACTGCACTCCA	4297
rs376865829	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118440361	CATTTTTTGCCTTTC[C/G]CCTTCCCTCTGTAGT	4297
rs376880734	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118462078	CGTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA	4297
rs376914389	snp	A/G	1.64942e-05	0.00287173	synonymous-codon, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520805	CTTATCTCTTAGGAG[A/G]GCAACTAGCATGGAT	4297
rs376927185	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118468199	TATCACAGGCATTTT[A/T]AAAATTATACCATAA	4297
rs376937581	snp	C/T	4.94197e-05	0.00497066	missense	KMT2A	GRCh38.p7	11:118506358	CCAACTTTACCCAGA[C/T]GGTAGACGCTCCTAA	4297
rs376974388	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118488995	AAAGTATATGGTGGG[C/T]GGATCACTTGAAGCC	4297
rs376986915	snp	C/T	4.94238e-05	0.00497086	missense	KMT2A	GRCh38.p7	11:118505728	TGGGGTCACTTAATA[C/T]TTCATCTCACCGAAC	4297
rs377066546	snp	C/T	1.6476e-05	0.00287014	missense, intron-variant	KMT2A	GRCh38.p7	11:118474160	TCTAGCACTGTTAAA[C/T]ATTCCACTTCCTCCA	4297
rs377089256	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118483406	GGCGAGGTGGCGGGC[A/G]CCTGTAGTCCCAGCT	4297
rs377156559	snp	C/T	4.94825e-05	0.00497381	missense	KMT2A	GRCh38.p7	11:118502481	AGCATTGGCTCCAGG[C/T]GTCACAGTACCTCTT	4297
rs377199235	snp	C/G/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118442042	TCTCTTTTGGAAACT[C/G/T]GCTGTGTTTTAATTG	4297
rs377204856	snp	A/G	3.30344e-05	0.004064	synonymous-codon	KMT2A	GRCh38.p7	11:118481842	AGAGGATCCTGCCCC[A/G]AAGAAAAGCAGTAGT	4297
rs377232966	snp	A/G	3.30573e-05	0.00406541	synonymous-codon	KMT2A	GRCh38.p7	11:118502711	TTTGCAAAGGACAGT[A/G]GTTACTGTAGGCAAT	4297
rs377278387	snp	A/C			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118517395	GGTGAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA	4297
rs377289398	snp	C/G	3.29734e-05	0.00406025	missense	KMT2A	GRCh38.p7	11:118504316	GCTCAGCTCATTGGA[C/G]TCAAGCCGCAGAGTC	4297
rs377361643	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118450545	ATTAAATATTTGAAA[A/T]CTGGACTTCATTCTT	4297
rs377388490	snp	C/G	1.65567e-05	0.00287716	intron-variant	KMT2A	GRCh38.p7	11:118468882	TGCCTTTTAAGTTTT[C/G]TTTGTTAGGAGATTG	4297
rs377410177	snp	C/T	0.000153988	0.00877328	intron-variant	KMT2A	GRCh38.p7	11:118510159	CATCAGCAGAAGCCC[C/T]GTTTCAGCTAGAGCT	4297
rs377416766	snp	C/T			missense, intron-variant	KMT2A	GRCh38.p7	11:118473720	GAAATAAAGACAAGG[C/T]CCCCGAGGAGCTGTC	4297
rs377462697	snp	A/G	4.94434e-05	0.00497184	missense	KMT2A	GRCh38.p7	11:118488711	AAAATTGGTGTTGTC[A/G]TCGTTGCAAATTCTG	4297
rs377478871	snp	A/G			upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118526602	AAAAAAAAAAAAGGA[A/G]AATGTGTCTAAAGTC	4297
rs377485215	snp	A/G	0.000214247	0.0103478	missense	KMT2A	GRCh38.p7	11:118491857	GAAAAAGAGCTGCAG[A/G]TTTCTCTGAAGCAAG	4297
rs377531018	snp	A/G	0.000296648	0.0121752	intron-variant	KMT2A	GRCh38.p7	11:118488591	ATTTGACATACTTCT[A/G]TCTTCCCATGTTCTT	4297
rs377564464	snp	C/T	1.64732e-05	0.0028699	synonymous-codon, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522043	GCAGAAGCACATTGT[C/T]ATCTTTGCCATGCGT	4297
rs377588214	snp	A/G	6.58935e-05	0.00573955	missense	KMT2A	GRCh38.p7	11:118496276	GTACTGATAGGAGTC[A/G]AGAAGACAGTCCAGA	4297
rs377663970	snp	G/T	1.65902e-05	0.00288008	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522176	TTCCTAAACTAAAGC[G/T]GCTCTTCTCCCCCAG	4297
rs377682443	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118453763	CTAACCTTCATGACC[A/G]TTGTCTGAAGTATCA	4297
rs377688685	snp	A/G	0.000153988	0.00877328	missense, intron-variant	KMT2A	GRCh38.p7	11:118472642	TCTCAGGCTTCTGAG[A/G]AGATTCAGGTACTTC	4297
rs377724112	snp	C/T	1.64762e-05	0.00287016	missense	KMT2A	GRCh38.p7	11:118493108	GAGAGTATACCTTCC[C/T]GCAGCTCCCCCGAAG	4297
rs377739026	snp	A/G	4.99721e-05	0.00499836	missense, intron-variant	KMT2A	GRCh38.p7	11:118473716	GGGAGAAATAAAGAC[A/G]AGGCCCCCGAGGAGC	4297
rs386757952	multinucleotide-polymorphism	CC/TT			frameshift-variant	KMT2A	GRCh38.p7	11:118502590	CCTCAGTCTCCACCA[CC/TT]GGGACCGCTACTGAT	4297
rs387907275	snp	C/T			stop-gained	KMT2A	GRCh38.p7	11:118503036	GGGCAAAGGAATGAT[C/T]GAGACCAACACACAG	4297
rs398122878	in-del	-/GTCT			frameshift-variant	KMT2A	GRCh38.p7	11:118504698	CCATCTGATCTGTCT[-/GTCT]TGACCACCCGGAGTC	4297
rs398122879	in-del	-/T			frameshift-variant	KMT2A	GRCh38.p7	11:118504159	ATGGAACAGAGAACT[-/T]AAAGATTGATAGACC	4297
rs398122880	in-del	-/T			frameshift-variant	KMT2A	GRCh38.p7	11:118502805	GTGTCCAAGAGCTCC[-/T]CTTTAAAGGGAGAGA	4297
rs398122881	in-del	-/T			frameshift-variant	KMT2A	GRCh38.p7	11:118490152	AAGTGTGTTCGCTGT[-/T]AAGAGCTGTGGATCC	4297
rs527261214	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118476624	GGCCTTTTTTTGTGC[G/T]GCCAATTAGGATACA	4297
rs527390222	snp	C/T	0.000122165	0.00781458	intron-variant	KMT2A	GRCh38.p7	11:118494801	ACTTTTTTTTCTCCT[C/T]ATCGGCTAGAAATCT	4297
rs527409576	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118438182	AGAAAAAGGATTATC[A/G]AGCAAAGTTATTCCT	4297
rs527465744	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118447978	AAAAGTACAGTCCTG[A/C]CTACATATGTATAAA	4297
rs527468385	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118437679	CAGCAGTCTCTTCCC[A/C]CCCCCGCCCCGTCTT	4297
rs527501404	snp	A/G	0.00011533	0.00759287	missense	KMT2A	GRCh38.p7	11:118502538	CGGATAATGTCTCCA[A/G]TGAGAACTGGGAATA	4297
rs527525816	snp	C/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118455967	GTGCTAGGATTACAG[C/G]CATGAGCCACTGTGC	4297
rs527567085	snp	G/T	0.00119737	0.0244387	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512806	TACCTGTTTTTTGTT[G/T]TTTTTTTTTTATTTT	4297
rs527569031	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522381	TCGAAGAAAAGATCC[A/G]TGATCGGCTTTCTCC	4297
rs527586731	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118455262	TAGCTTCATGGGGCA[A/G]GAATTTTGTTAGTTC	4297
rs527590550	snp	C/G			upstream-variant-2KB	KMT2A	GRCh38.p7	11:118434495	GAGAGAGAGAGAGAA[C/G]GAACAAATCAGGATG	4297
rs527627532	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118507911	GAGCTTGCAGTGAGC[C/T]GAGATCGCGCCACTG	4297
rs527657640	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118465327	ATGTTTCAGTTCCCA[C/T]GACCCCCAGTTCTTT	4297
rs527671779	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118478911	ACAAACATGAGCCAC[A/G]GTGCTTGGCCTCATA	4297
rs527914982	in-del	-/A	0.299158	0.245119	intron-variant	KMT2A	GRCh38.p7	11:118464540	GGGAAACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	4297
rs527937874	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118436335	CCCGAGGCCGCTATA[C/T]AGATTGCGGGGCTGG	4297
rs527957871	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118501221	GCAGCACTTTGGGAG[G/T]CTGAGGCAGGTGAAT	4297
rs527969472	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118492275	GGACTGGAGACACCT[C/G]AGCCTAGAGGCAGGA	4297
rs528016297	snp	A/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118445937	TGAACCCAGGAGGTG[A/G]AGGTTGCAGTAAGCT	4297
rs528018032	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118511640	ATACCAAACATTCAG[A/G]TGTGAGACCCAGACT	4297
rs528030892	snp	C/G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118500446	TTTTGCAATATATGC[C/G/T]CCAACTTACTCTGTA	4297
rs528044061	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118478829	GACATGATCATAGCT[C/T]ACTGCCAACACTGAA	4297
rs528066201	in-del	-/A	0.0551013	0.156571	intron-variant	KMT2A	GRCh38.p7	11:118486711	GACCTCATCTCTACT[-/A]AAAAAAAAATAAAAT	4297
rs528092574	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118510676	CAGCGAGCTCTCCAT[A/G]AGGGCTGGAATTTTA	4297
rs528137662	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118443997	TAGAGAGATCCACTT[A/G]TATTATCTATGCTTT	4297
rs528158809	snp	C/T	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118509738	GAGAGCATAACTTCA[C/T]GTAAAAAAAAATCTG	4297
rs528186276	snp	A/G	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118471125	AGTAAAACTTTCTTA[A/G]TCTACTTTGGCAAAA	4297
rs528219220	snp	C/T	0.0460142	0.144533	intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118518947	AGCCAGGCGTGGTGG[C/T]GGCGCCCGTAGTCCC	4297
rs528244377	snp	A/C	3.29484e-05	0.00405871	missense, intron-variant	KMT2A	GRCh38.p7	11:118473916	GAAGGTTGTTGGTGA[A/C]GATGTTGCCACTTCA	4297
rs528322887	snp	C/T	6.61956e-05	0.00575269	missense, intron-variant	KMT2A	GRCh38.p7	11:118472610	CTAGTAGCCCCAGTG[C/T]TGATACCTCCACAGA	4297
rs528361199	snp	C/T	1.65127e-05	0.00287334	missense	KMT2A	GRCh38.p7	11:118481814	CTAGTCAGAAACCTA[C/T]CCCATCAGCAAGAGA	4297
rs528392910	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118486710	GACCTCATCTCTACT[-/A]AAAAAAAAAATAAAA	4297
rs528399568	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118507240	GAGTTAGAGGCTAAA[A/T]GATCCATGGTCATGT	4297
rs528422578	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118490486	GAAATCCTCTAAGCT[A/G]GTATTTCCCAAAGTG	4297
rs528424399	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118480796	GCCTCCCTAGTAGCT[A/G]GGACTACAGGTGCGC	4297
rs528567888	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118498663	ATGCACAGCCTCCCC[A/C]ATGATCAGCATCCCC	4297
rs528619665	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118497819	TCTGTGTGCCTCCCT[C/T]CATTAAAGAATTATA	4297
rs528626983	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118508274	ATACTGTACATACTG[C/T]TCTGTATTTGGTTTT	4297
rs528682281	snp	C/G	1.65405e-05	0.00287576	missense	KMT2A	GRCh38.p7	11:118507577	AGCTAGCGTGGAGCA[C/G]TCCTCCCAGAAGGAG	4297
rs528768227	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118454923	TAGTTTTCCAGTCTT[C/T]GGTAAACTATTGCCT	4297
rs528772375	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118459774	GCCCTCCCAACCCCC[C/T]GCCCCGGGTTCAAGC	4297
rs528822610	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118526156	GGGGGGAACCTCTAA[C/T]CATAAAGGAATGGTA	4297
rs528831980	snp	C/G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118458718	AAGACCTTGGTATTT[C/G/T]GAAGCTTGTAGCAGT	4297
rs528885633	snp	A/T	0.0023933	0.0345097	utr-variant-3-prime, intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118524818	CAGGGGGTGGGGGGA[A/T]CTCAGCTAAATAGAC	4297
rs528888707	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118442602	TCCTAAGTTGTATCG[A/G]CTTTGAGACACAGAC	4297
rs528901222	in-del	-/T	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118450723	TGTTATGCATTCAAA[-/T]AATCATTGTTCTCTT	4297
rs529001696	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118475773	CCTAGGGCCATAGTT[-/A]CATTTACTAATTCTG	4297
rs529146122	snp	C/T	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118441063	GCTCATGAATCTGTT[C/T]TGTGTCAGTATTATG	4297
rs529166709	snp	A/C	3.29468e-05	0.00405861	missense	KMT2A	GRCh38.p7	11:118506343	CAGGGCCCCAGGTAT[A/C]CAACTTTACCCAGAC	4297
rs529182127	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118495569	CAGCAATTTTCAAAC[G/T]CTGTGACTTGTTCTT	4297
rs529259508	snp	A/T	0.00398564	0.0444627	intron-variant	KMT2A	GRCh38.p7	11:118493898	GTATTTTTGGCGGAG[A/T]TTGGGTTTCACCATG	4297
rs529275565	snp	A/T	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118444643	TGTAATGGCACAAAC[A/T]TTTCATTTCAGCCTC	4297
rs529276917	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118514758	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA	4297
rs529290401	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118448970	AACAAGAGATGTAAA[A/G]TTCATAAAACTGCTT	4297
rs529311706	snp	A/G	0	0	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118523218	CCAGGATGACCCTTG[A/G]GTCCCATTCCTAAGA	4297
rs529332464	in-del	-/A	0.263809	0.249618	intron-variant	KMT2A	GRCh38.p7	11:118508721	GTGAGAACCTATCTC[-/A]AAAAAAAAAAAAAAA	4297
rs529379599	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118498270	AATAGATAAAATGAA[C/T]TGTAGGAACTGTAGA	4297
rs529484845	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118466445	TACAGGTATGAGCTA[C/T]TGTGCTGGCCAAGAG	4297
rs529588768	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118475815	TTGTAGCAGGAATGT[A/G]ATGGGACTTATTTTT	4297
rs529594365	snp	A/T	0.00517822	0.0506191	intron-variant	KMT2A	GRCh38.p7	11:118489141	GGGAGGAAAATCGCT[A/T]GAACTTTGGAGGCAG	4297
rs529612382	snp	C/T			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118525293	GAGCCAGCTCACTTA[C/T]AGCTTTGCTGCTAGA	4297
rs529709559	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118437611	AAATCTCTCCTCTGC[A/T]CCTTGCCTGGTCTCA	4297
rs529766983	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118447116	AAGTTTTCACAGATT[G/T]TACTGCTAGTTGAAA	4297
rs529772045	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118464391	AAATACAAAAATAAC[C/G]AGGTGTAGTAGTGCA	4297
rs529789387	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512672	GGAATGGCTGGGTCA[C/T]ATGGTAACTCTTTAA	4297
rs529812808	snp	A/C	0.00597247	0.0543191	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118436447	GGCCCCGTGCCCCCC[A/C]CTCCGCCTCCCCGCC	4297
rs529816474	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118455192	CACCATGCCCAGCCC[C/G]TAGTGTCTTTTATTT	4297
rs529886909	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118454413	GCCTTTGCACTTGCT[C/G]TCAGGCTAGAACACT	4297
rs529950159	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118464059	ATAAATAATTGGATG[A/G]CTCATTTTAAGAAGG	4297
rs529963620	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520747	AACCTTCGATTCAAG[A/T]CTCAAAACATTATTT	4297
rs530010374	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118463092	GTTGTTAATAATGAA[C/T]CTAACAGTGTGTATC	4297
rs530017751	snp	C/T	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118474774	GGAGGGGAGCATTCT[C/T]TTCCTCTGAGTAGTG	4297
rs530083042	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118474725	ACATTTTAATAGTCA[A/G]ATTGTTTTACTATCC	4297
rs530090576	snp	G/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118516848	CTTCCTCTGCTGTGA[G/T]CTCCTTAAGAACAGA	4297
rs530225101	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118435300	TTTCCCGCAATAAAG[A/T]AAACCCGGTGGATAT	4297
rs530268183	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118492146	GTTACAATGAGAAAT[C/T]TGGACTTTATACTCT	4297
rs530283719	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118434652	CTTAGCAGAGCCTTG[C/G]GGCTGCCGTTTAAGA	4297
rs530304742	snp	C/T	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118510536	AAGATCCAGCTCAGA[C/T]GGTCTTCCCTGACCT	4297
rs530304747	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118486455	AAGTAGCACAATTTT[A/G]AATAGGAAGCAGTAG	4297
rs530307162	in-del	-/AAG			intron-variant	KMT2A	GRCh38.p7	11:118482780	AAGAAGAAGAAGAAG[-/AAG]TTAGCCAGGCATGGT	4297
rs530333520	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118500416	CCCTTCTACCACTCC[C/T]GCGTTGGAGTCTCAT	4297
rs530393782	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118499751	CGCCACTGCATTCCA[G/T]CCTGGGCGACAGAGT	4297
rs530436523	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118443877	TAGTGTTTTATCCAT[G/T]TTCTTGCATTTCTGG	4297
rs530454631	in-del	-/T	0.00199481	0.0315187	intron-variant	KMT2A	GRCh38.p7	11:118491992	TACCTAGTGTTTTTC[-/T]TTTGTTTTACTTCAT	4297
rs530496789	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118465153	TGAGGCAGGAGAATC[A/G]CTTGAACCCAGGAGA	4297
rs530504213	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118452778	AGCTGGGATTACAGG[C/T]GCCCACCACCACGCC	4297
rs530561756	snp	G/T	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522229	GCCATCCAAAGCAAC[G/T]CTGAAGGCCTTTTCC	4297
rs530572017	in-del	-/C	0.00160489	0.0282819	intron-variant, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118511926	ATATTTTCTGGCTTA[-/C]CGGGTTTTCTTTATT	4297
rs530574757	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118506790	TTTGACTTTTTTTCT[C/G]TCTGAGTGGTGATTT	4297
rs530639255	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118510601	TGAATCTTACATGTT[C/G]TTCTCTCATAGCTTA	4297
rs530639306	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118459701	AATGGAGTCTTGCTC[C/T]GTTGCCCAGGCTGGA	4297
rs530642780	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118471204	TGATTGAAGAGCAGC[A/G]TATTCAAATTTGTTC	4297
rs530687517	snp	A/G	0.00318978	0.0398085	intron-variant	KMT2A	GRCh38.p7	11:118471042	TATGTCACTTCACTG[A/G]TTAGTTCACATGCCA	4297
rs530714844	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118479784	TTATAGTGGTAGACA[A/G]AGGAGTTGTTTGATA	4297
rs530763781	snp	C/T	0.000251465	0.0112102	intron-variant	KMT2A	GRCh38.p7	11:118488495	CTTAATGAATATGTA[C/T]TGAATTAAATATATG	4297
rs530827450	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118497658	CCACTTCAGCCTCCA[A/G]AAGTGCTGGGATTAC	4297
rs530833253	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118489429	GTATTTCTGTCTTCC[A/G]GTTAAGATTTTGTAT	4297
rs530890904	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118507446	TCAGATCCTGATAGA[C/G]CCATTTCTTTCGACT	4297
rs530984888	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118459599	AGTAGCTCTGGAGCC[G/T]CCATCTTAGCCTGGT	4297
rs530992035	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118450059	TTATGGTACTTTCCT[A/G]TTAGAGAAAAATAAA	4297
rs531051778	snp	G/T	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118453585	TCCAGGCCTCATCTA[G/T]ACGCTGACAACTAAG	4297
rs531063854	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118493342	AATTGTATTATATTT[A/G]GAAATGTCACGTGGC	4297
rs531074720	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118516721	TTATTGAATGAATAA[A/G]TGAGTCTCCCACAAG	4297
rs531079455	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118524496	ATGCAGGGAGCCCAG[C/T]ACTGTGGCCAGGATG	4297
rs531138900	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118526010	AGGAACTAATATAGT[A/G]ATGCACCATGTAACA	4297
rs531234554	snp	A/G	0.00199481	0.0315187	intron-variant	KMT2A	GRCh38.p7	11:118477609	ACTTCCCAGGTTCAA[A/G]CGATTCTCCTGCCTC	4297
rs531301091	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118478437	TATTGGAATAGTAGA[C/G]AACAATAATGGAAAT	4297
rs531372480	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118487466	TGATTTCAGACTTAC[A/G]AAAAAACTATGAGTT	4297
rs531391885	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118439503	GGGACCTAATGTCTG[A/G]GCACCAGAATATTTT	4297
rs531421006	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118508857	CCTTTCATTTTTTTC[C/T]AATACTGAGTATGAG	4297
rs531494566	snp	A/G	1.65762e-05	0.00287886	missense, intron-variant	KMT2A	GRCh38.p7	11:118471886	GGAAAGGACATTTCA[A/G]AGTTACCAAAGGGAA	4297
rs531496642	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118495536	GATATTTTTTAAAAT[A/G]TTGAGTTCTGTGTAC	4297
rs531526377	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118448045	GTAAATAAATTCTTA[C/T]TCAGCTCCTCGAAGC	4297
rs531555284	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118513942	GACCCTGTCTCAAAA[A/G]AAAAAAAAAAAAAAA	4297
rs531588793	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118448839	GTTGGCAAAGCGAAG[A/G]GCAGTTTGACTCCTT	4297
rs531618181	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522562	TTTCCCAAGCACTGT[A/G]AGTGAGTGGGTCAGG	4297
rs531620249	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118514638	TATTTTTTTATTTTT[A/G]TTTTTATTTTTTGAG	4297
rs531632658	snp	A/G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118452868	CGAACTCCTGACCTC[A/G/T]TGATCTGCCCACCTC	4297
rs531712610	snp	C/G	0.00656237	0.0569045	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118435087	GCTGTACCGGTGCGG[C/G]AGTCCAGGAAGGCTG	4297
rs531789163	snp	A/G			upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118525644	AAATACAACACACAC[A/G]CAAAAATAAAAAAAA	4297
rs531798430	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521639	TCTGAGTGGCTCCTA[A/G]TATCAGAAGCAAATA	4297
rs531942770	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118502317	AAATATATATATATA[G/T]AGTCAAATCATTGAA	4297
rs531946287	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118485791	GGGTTAAAATAAGCA[A/T]AGGGCATATAGCTGG	4297
rs532004906	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118501398	CACTTGAACCAGGGA[A/G]GCAGATGTTGCAGTC	4297
rs532064851	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118511772	GGGAGTGTACCTTTT[C/T]GGCTCCTTTCACATG	4297
rs532091956	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118492736	CAGAGCTAAGCTGCT[A/G]TTTTATCTTTTAATA	4297
rs532224828	snp	C/G	0.000798403	0.0199641	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512276	ATCCCTAAAAGAAAC[C/G]CCCTATTCATTAGCA	4297
rs532262645	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118445210	CTAGGTGGAACCAAA[C/T]TGAAGGCCAGCCACC	4297
rs532288058	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118516409	TTATAGTGTGCCAAG[A/G]TCATACCTGTGAATA	4297
rs532317440	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118453971	CATGTAAGATTTATC[A/G]TCGATTTATCTCTTT	4297
rs532343313	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118482795	AAGTTAGCCAGGCAT[G/T]GTGGCAGTTGCGTGT	4297
rs532343835	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519845	CGATTTTCTTATCTC[A/C]TGACACTGTCATCTT	4297
rs532377501	snp	C/T	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118462875	CCTGACTACTTATTT[C/T]TTATTTCCTTATTCC	4297
rs532434991	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118491996	TAGTGTTTTTCTTTT[G/T]TTTTACTTCATTCTC	4297
rs532492158	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118434492	AGAGAGAGAGAGAGA[A/G]AACGAACAAATCAGG	4297
rs532551039	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118443838	AGTAGCATTTATTTC[A/G]GGAGCTGGAGTTTCT	4297
rs532620650	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118498878	TCCTCTGTGCTCTGC[A/C]TATTCATCCCTGCCT	4297
rs532621703	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118443132	CCTAATTCTCTAATT[A/G]CTGGCATTTATGACA	4297
rs532769398	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118455170	AGCTAGGATTACAGG[C/T]GAGAGCCACCATGCC	4297
rs532773133	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118509356	TGGACTGAAACTTGG[C/T]GCACCTGTCTCTCGG	4297
rs532841731	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118518859	AAGGCGGGTGGATCA[C/T]GAGGTCAGGAGATCG	4297
rs532856607	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118526211	GAAAAATGCAGACAT[A/G]GTGTCACCTGGATTT	4297
rs532900326	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118498984	GAATCATATAGTACA[C/T]AGCCTTTTCAGACTG	4297
rs532921889	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118460805	CCAAATAGTTGGGAC[G/T]ACAGGCGCACACCAC	4297
rs532935420	snp	G/T			missense	KMT2A	GRCh38.p7	11:118504219	CTAAGAGTTCTGTTG[G/T]CCACAAAAATGAGCC	4297
rs532948634	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118527153	GTATTGATTTTTATC[A/G]GTTTTCTCAACTGTG	4297
rs532983949	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118458615	TCAGAGTACACACTC[C/T]AAAGAAGACAAATGT	4297
rs532991008	in-del	-/A	0.385741	0.209939	intron-variant	KMT2A	GRCh38.p7	11:118449585	GTGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA	4297
rs533037781	snp	C/T	0.000658718	0.0181363	synonymous-codon	KMT2A	GRCh38.p7	11:118476876	CTGCAGAAGAGCAGC[C/T]GTTGCCCTTGGCCGA	4297
rs533041122	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118499521	AGGTGTGGTGTCTCA[C/T]GCCTGTAATCCCAGC	4297
rs533072595	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118487688	TTTAAAAATCAAGGA[C/T]GTTCTCGTATTTAAC	4297
rs533098181	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118444600	GGTTTGTTTGAGACA[C/G]GATCTTGCTTTGTTG	4297
rs533133663	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118496658	TCTAATGGAAGTTCC[C/T]CAAGAATATTTTGTG	4297
rs533185127	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118488391	TGTATTATATTTATT[A/T]TGTTACTTTCTATTT	4297
rs533235014	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118515953	TTGGCCTCCCAAAGC[A/G]CTGAGAGTACAGGTA	4297
rs533348482	snp	C/T	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118492437	GTAATCCCAGCACTT[C/T]GGGAGGCCGAGGCGG	4297
rs533392657	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118467454	TTCTTAAATAGTCCA[A/G]TACTTTAATCTTAGC	4297
rs533411416	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118450089	ACCCTGTGATTGTGA[A/T]GCTTAACTTAATTTT	4297
rs533440802	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118477434	GGTTTCTATTCTCGA[C/T]TTTAGATTAGACTTT	4297
rs533476111	snp	A/G	0.0023933	0.0345097	intron-variant	KMT2A	GRCh38.p7	11:118458374	TTTCAGGTGTGAGCC[A/G]CCTCGTCCTGCCCCT	4297
rs533478161	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118449361	CCAGGAGTTCAAGAC[C/T]AGCCTGGGCAACTTG	4297
rs533517533	snp	C/T	0.00199481	0.0315187	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118524254	TCTCTGCCTCTGCCA[C/T]AAGGTTTCAGAGTAG	4297
rs533523277	snp	G/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118465870	TCATTATTGTGATAA[G/T]ATTTTATATTAATTG	4297
rs533671138	snp	A/G			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118523052	GTGGGGAAGTGGACA[A/G]GAGCCATTGGTCATA	4297
rs533693209	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118488111	CTTGAACCCAGGAGG[C/T]GGAGGTTGCAGTGAG	4297
rs533795027	snp	C/G	0.000515929	0.016053	missense	KMT2A	GRCh38.p7	11:118436739	GGGCTGGGGTTCCAG[C/G]GGGAGCGGCCGCCGC	4297
rs533826575	snp	C/T	1.65927e-05	0.00288029	missense	KMT2A	GRCh38.p7	11:118501843	CCCCTGGCTGTCGAC[C/T]GTTGCCTTCTGCAGG	4297
rs533904103	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118445465	AACAGCTCTGAGGCT[C/T]TTCAGGGTTCTTGGG	4297
rs533904194	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118454537	TTGAAACTACTCCAC[C/T]CTGTTGTTGTAAGTG	4297
rs533984034	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118488770	ACAAAGGTACAAAAC[C/T]TGGTAATAGAACTAC	4297
rs534030002	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118463158	AGATGGGGTCTTGCT[A/G]TGTTGCCCAGGCTGG	4297
rs534039039	in-del	-/T	0.396182	0.202807	intron-variant	KMT2A	GRCh38.p7	11:118453401	CACTCCCTTCTTGGA[-/T]TTTTTTTTTTTAACA	4297
rs534077210	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118492514	GAAACCCCGTCTCTA[C/T]TAAAAATACAAAAAA	4297
rs534088699	snp	A/C	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118474401	AAGTGGTTCAATTAC[A/C]TCCAGTTATGAGAAC	4297
rs534092128	in-del	-/T	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118470680	TCTGTTAGCAAGCAG[-/T]TCCATTGTAAAAATG	4297
rs534103703	snp	A/C/T	0.000798403	0.0199641	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118435823	TTTTTAAAGTGCGTT[A/C/T]ATTGAGGGCCTTTCT	4297
rs534190752	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118511222	TATTGCTAGAGTAGA[A/G]ATGTCTGGTAATAAA	4297
rs534370076	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118462679	TTCTCCTGCCTCAGC[C/T]TCCTGAGTAGCTGGG	4297
rs534394153	snp	C/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118513049	TTCAAGACCAGCCTG[C/G]GCTTCATACAGAGAA	4297
rs534491697	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118442506	GAGTAAAATATTGTC[A/G]TGGAGTAAATCTCAG	4297
rs534519600	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118518597	ACCAGCCTGGCCAAT[A/G]TGGTGAAACCTTGTC	4297
rs534525295	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118507942	CACTCCAGCCTGGGC[A/G]ATAGAGCAAGACTCC	4297
rs534577734	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118517696	AATTTAAAAATTAGC[C/G]AAACACAGTGGCATA	4297
rs534620846	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118490255	TTTGCTAAAGGTACC[C/T]AAAAAAGCCAGTTTT	4297
rs534705759	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118497527	CAGCCTCCTGAGTAG[C/T]TGAGACCACAGATGC	4297
rs534714984	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118443347	ATGATGAGCCGCTTT[C/T]CTTGACCTATCCAAA	4297
rs534715283	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118479965	ATAATTTGATATTTG[C/T]TCCTTTTAGATCCTA	4297
rs534761797	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118508728	CCTATCTCAAAAAAA[A/G]AAAAAAAAAGGTGAA	4297
rs534797226	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118459922	ATGGTCTCAAACTCC[C/T]GACCTCAAGTGATCT	4297
rs534834830	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118487857	ATTTTTGAAAATCCT[A/G]TATCAATATGAAAAT	4297
rs534847809	snp	C/T	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118451699	GGTCTCACCATCTTA[C/T]GTAGCTGGTCTCGAA	4297
rs534894171	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118496915	GTATGTAAAGCCTCT[A/G]TTTGGTGCCTGGCAC	4297
rs534969722	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118495983	TAAAATTAGATATAC[C/T]TGGATATCAGAAAGG	4297
rs535019591	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118440489	GACTAGAAGTTAGGC[A/T]GTTGTAATAATAAAC	4297
rs535053025	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118449694	TAATTTTACACTGCT[C/T]CTTCAGCAAACTGAC	4297
rs535069551	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118447060	CTTATTATTCGTCTC[C/T]CATGGTTCAACTCAG	4297
rs535164148	snp	G/T	3.4114e-05	0.00412987	intron-variant	KMT2A	GRCh38.p7	11:118489741	CTAAGTAATAGGTGT[G/T]GGGTGAAGGTAATAT	4297
rs535170983	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118456679	TATTCCTCAGAACTC[A/T]GCCATCTACCCTCCT	4297
rs535198027	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118443163	GTGTGGATGCTACTG[A/G]CCCTGTGGCTGAGGT	4297
rs535265349	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118441416	TTCATTTATAAGAAA[A/G]ATGAGGATAAAGTTT	4297
rs535515166	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118523650	ATTTTTTAAACCGCG[A/G]TATTATCCTAATTTA	4297
rs535525227	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118437693	CCCCCCCGCCCCGTC[A/T]TACAGGGCTACAGTT	4297
rs535531404	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118467889	GAATCTGAAATTCTA[C/T]CATTCTGTGTCTGTC	4297
rs535588825	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118447468	ATTTAAGTATGGCAA[A/G]GGAAAGCACAGGTGC	4297
rs535596785	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118477687	TAATTTTTGTATTTT[C/T]AGTAGAGAGGGGTTT	4297
rs535604901	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512999	ATCCCAACACTTTGG[A/G]TGACCAAGGCAGAAG	4297
rs535704325	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521198	GTCCCTCCTGGGGAA[C/T]TAACAGACCAGGAGA	4297
rs535790312	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118485479	TTTTTAGCCCTCTAG[A/T]GACCAAAAACTGGAA	4297
rs535839795	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118457043	TTTTCCCCTTAATCC[A/G]TATGGCCACTACAGT	4297
rs535847778	snp	C/T	3.29864e-05	0.00406105	missense	KMT2A	GRCh38.p7	11:118504216	TCACTAAGAGTTCTG[C/T]TGGCCACAAAAATGA	4297
rs535885436	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118442324	GTTTGCATATGTTAT[C/T]TTCAGGGATTAAGAA	4297
rs535920328	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118492790	AATTAGCTGCTTTCT[A/G]TGTTAAAAGGAACTG	4297
rs535975716	in-del	-/A			upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118526587	GTTAGAGAAAAAGAG[-/A]AAAAAAAAAAAGGAA	4297
rs536031523	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118455535	ACCATACAAGAATTA[A/T]CAAGGTTCTGATTAT	4297
rs536038552	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512338	TACTTTCTGTCTCTA[C/T]GTATTTGATTATTCT	4297
rs536039449	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118484556	CTGAGCAGTATCAGA[A/G]GAAGTAATTCCTTCA	4297
rs536042773	snp	G/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118500648	TACTTTGTATACATT[G/T]TAAGGCAATAGTTCG	4297
rs536124980	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118511155	GCTCTCTATATGAGA[C/T]AGATTGAGCATGAAC	4297
rs536152267	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118453711	TGTTTATTGTGGGCC[A/G]GGCTATATTCTGAGC	4297
rs536154032	snp	A/G	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118464625	ATCAGCTGCAGACAA[A/G]TGTAGAGCATTCAAT	4297
rs536218759	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118452989	TCTGGATCCCATCTC[C/T]TCTCATCTAGTCAGG	4297
rs536229197	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118467463	AGTCCAATACTTTAA[C/T]CTTAGCAATCTCAGA	4297
rs536238765	snp	C/T			intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118518954	CGTGGTGGCGGCGCC[C/T]GTAGTCCCAGCTACT	4297
rs536259110	snp	A/G	0.00159617	0.0282053	intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118518940	AAAAATTAGCCAGGC[A/G]TGGTGGCGGCGCCCG	4297
rs536265496	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118474581	TACTGGATAGCTGGA[A/T]TGGCATCTGTGGAAA	4297
rs536283415	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118462589	TTTGAGACAGAGTCT[C/T]GCTCTGTCGCCCAGG	4297
rs536324387	snp	A/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118483498	AGATCGCGCCACTGC[A/T]CTCCAGCTTGGGTGA	4297
rs536366797	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118461279	AATTTAGTGGTAAAG[G/T]TATGCTTGGAAGCTC	4297
rs536367085	snp	G/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512504	GCCAAATATTCCATT[G/T]TGTAGATATACCATA	4297
rs536418114	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118474872	GCTCATGCCTGTAAT[A/C]CCATCACTTTGGGAG	4297
rs536475692	in-del	-/A	0.00199481	0.0315187	intron-variant	KMT2A	GRCh38.p7	11:118482258	TAAAGAAACAGAAAC[-/A]AAAAAAAACAGTTAA	4297
rs536639703	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118519188	TTATATTTGTAGTTA[G/T]GCAGTCCAGAGTTCA	4297
rs536644786	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118508622	CATCCACAGTCCAAG[A/C]TAAGGCGGGAGGATT	4297
rs536815209	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118471318	CGAGGAAGTTCAGAT[G/T]TTTTTTCTTTACAAT	4297
rs536818082	snp	A/T	0.00279162	0.0372561	intron-variant	KMT2A	GRCh38.p7	11:118450644	TCCCAAGTGACCTTT[A/T]TGTGTTAACATTTCT	4297
rs536867346	snp	A/G	0.00279162	0.0372561	intron-variant	KMT2A	GRCh38.p7	11:118481297	TCTGTCTCTATCTCC[A/G]TAAGTTCAATTGTTT	4297
rs536899540	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118525236	AGGGGCATCCCAAAT[C/T]CCTGAGGAGTAACAG	4297
rs536983420	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118499000	AGCCTTTTCAGACTG[A/G]CTTCTTCTGCATAGC	4297
rs537074714	snp	C/T	0.000230593	0.0107351	synonymous-codon	KMT2A	GRCh38.p7	11:118478109	GTGTGGGCAGTGTCC[C/T]GGCTGCCAGGTGCCT	4297
rs537090552	snp	A/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118442460	AAAGTATTTCCTTGG[A/T]TCTTATCTAGACTGG	4297
rs537112945	snp	A/G	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118507827	AATTAGCCGGGCGTG[A/G]TGGCGGGCGCCTGTA	4297
rs537123033	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118496735	ATAGGATAGCAGAAT[C/T]GTTAAGAGCCCGAGT	4297
rs537125451	snp	A/G	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118487179	TGTATCCTCTTTTCC[A/G]TCTTAATACAGTGCT	4297
rs537152459	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118451683	TTTTTTGTAGAGATG[A/G]GGTCTCACCATCTTA	4297
rs537181053	snp	A/T	0.00119737	0.0244387	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118517245	CTAAAAAATACAAAA[A/T]ATTAGCCAGGCGTGG	4297
rs537226064	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118451855	TATTCACATTTTTAA[C/T]ACTTTGCAAGATACT	4297
rs537245615	snp	C/T	3.29582e-05	0.00405931	synonymous-codon	KMT2A	GRCh38.p7	11:118503947	CGACTTATACTATTA[C/T]AACTTCACTAGAACA	4297
rs537250793	snp	C/T	0.000461148	0.0151777	missense	KMT2A	GRCh38.p7	11:118505854	CGGCAGGCACATCAA[C/T]AATAAGCCAGGATAC	4297
rs537310820	snp	A/G	1.64876e-05	0.00287116	synonymous-codon	KMT2A	GRCh38.p7	11:118504793	AGTAACCATCACAGA[A/G]AAATCTGTAGCCTCC	4297
rs537345741	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118448393	GTTAGTTAGTATTAT[A/T]AAAGCCTCTGACCCT	4297
rs537370162	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118514295	TGCTCTTTGAGGTTT[C/T]CTGTCTACGGATCCT	4297
rs537400950	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118469586	CAATGGAAATAACAT[C/T]TAATGGCTTGCCTAA	4297
rs537408474	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118456626	TACAGGCATGAGCCG[C/T]CGCGCCTGGCATGCC	4297
rs537413789	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118478733	TGTGCTTTCTCACTC[C/T]CTCTTAGAATATGTT	4297
rs537434700	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522942	TCCCATGCTTCTTTC[A/G]GGTTGTAGGGGAGAC	4297
rs537473001	snp	A/C	0.000801764	0.020006	intron-variant	KMT2A	GRCh38.p7	11:118466802	AGACTCTGCCTCAAA[A/C]AAAACAAAACAAAAC	4297
rs537525713	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118481629	CTAGCTGTGGGATTG[A/C]TGGATCATATGGTGG	4297
rs537669083	snp	A/G	0.00318978	0.0398085	intron-variant	KMT2A	GRCh38.p7	11:118485324	AAAGCCTCTTCATCT[A/G]TAAGGAGCTCTTACC	4297
rs537682548	snp	A/T	0.00199481	0.0315187	intron-variant	KMT2A	GRCh38.p7	11:118438858	GCGTGTTCCTTGCTA[A/T]GTAGCTAGCTGCAGC	4297
rs537736391	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118494085	TGTTTGCATTCTTAC[A/C]TCATTAGCCTGGCAT	4297
rs537751943	snp	A/G	0.00318978	0.0398085	intron-variant	KMT2A	GRCh38.p7	11:118457753	GCTTTATCATCCTTC[A/G]AAAGATTAAGTTTTC	4297
rs537778603	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118523557	CAGTTTACTATTTAA[C/G]GTTTTATAAATGTAA	4297
rs537829994	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118437064	GGGGTCCCTGACCCG[A/G]GGCGAATGGCTCTCC	4297
rs537890035	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118446697	TTTGGATAGTTTATT[A/G]TGGTAATCTTCTCAT	4297
rs537954683	snp	A/G	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118454673	ACTTACAAGCTCGTC[A/G]TAAAGTCAAAAATTG	4297
rs537983656	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521098	CTGCTTCCAGCGGGT[C/T]ACAGAATGGAAATAA	4297
rs538002696	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118494775	TCAAGCAAGTAAGTG[A/T]ATTTAGCATAACTTT	4297
rs538019539	snp	A/C	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118440154	AATGACTATAACTTG[A/C]CTATGTAACAACACC	4297
rs538191855	snp	C/T			upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118526567	TGTGTTCTTCCAAGC[C/T]TCTGGTTAGAGAAAA	4297
rs538201176	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118450195	AGGATTCTGGAAATA[C/T]ACCTTTCTTGAGTTT	4297
rs538217487	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118483461	TGGCGTGAACCCGGG[G/T]GGCGGAGCCTGCAGT	4297
rs538244548	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118501961	TTTACTGATTGAAAA[C/T]GTAGATTCCGGGTGG	4297
rs538246362	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512874	TGAAATCATTTACCA[G/T]TGGTATTAGACTTCA	4297
rs538280193	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118492401	AGAACCACACGGGGC[C/T]GGGCGCGGTGGCTCA	4297
rs538394110	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118500025	CTTTAAACTGCTACT[A/G]AAAATTAATCACTTA	4297
rs538398682	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118453860	TCTCTTACTTACCAT[A/C]TCTAAAAAGTCTTGA	4297
rs538407706	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118464534	GCAAGAGGGAAACTC[C/T]GTCTCAAAAAAAAAA	4297
rs538425365	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118475559	AAACCCTGTCTCTAC[C/T]AAAAATCCAAAAAAT	4297
rs538425507	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520388	CCAGGCACAGTGGCT[A/C]ATGCCTGTAATTCCA	4297
rs538430308	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521807	ACTTTCTCAGCCGCT[A/G]TAGGTAACATCAAGA	4297
rs538467372	snp	C/T	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118474993	AAAAAATTAGCTGGG[C/T]GTGGTGATGCATGCC	4297
rs538469129	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118463332	TTATATGTATAGTTG[C/T]TTGAGCTGTCAATCA	4297
rs538498991	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118452874	CCTGACCTCGTGATC[A/T]GCCCACCTCGGCCTC	4297
rs538509376	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118448529	ATTGGGATTATTCAT[A/G]TAGATTACCAAAAGT	4297
rs538512659	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118457194	GGATGAGGTCTACAC[A/G]TCCTCAAAGATAAAC	4297
rs538560726	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118462473	GTACTTATTTTTTAA[A/G]GCATGCTTCAAGAAA	4297
rs538565391	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118518281	AATGGAAAAAGCCAA[A/G]TAATTTTAAAATGAA	4297
rs538641774	snp	A/G	0.00199481	0.0315187	intron-variant	KMT2A	GRCh38.p7	11:118507693	TTCCAGGCCGGGCGC[A/G]GTGGCTCACGCCTGT	4297
rs538651796	snp	G/T	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118482327	AGTTTAAATAGTTTT[G/T]TTTTTTTTTTTCTAA	4297
rs538687700	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118435508	CATACATTAGGGTCT[A/G]CTTTGCATGCAGCGG	4297
rs538714509	snp	A/T	1.64735e-05	0.00286993	missense	KMT2A	GRCh38.p7	11:118491810	GTGTGAACTGTACTG[A/T]GCGGCACCCTGCAGA	4297
rs538751569	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118434996	GGAGGGCCAGAGCTG[A/C]GTGCAACCTGCTCAC	4297
rs538804060	snp	A/G/T			intron-variant	KMT2A	GRCh38.p7	11:118458379	GGTGTGAGCCACCTC[A/G/T]TCCTGCCCCTATACA	4297
rs538817636	snp	A/C	1.65031e-05	0.00287251	missense	KMT2A	GRCh38.p7	11:118489807	CAGCTGCTGGAGTGT[A/C]ATAAGTGCCGAAACA	4297
rs538880753	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118460910	GTCTGCCTTAGATAC[C/T]TCTTGGGAGCAGGAA	4297
rs538930086	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118452212	CGTCTGGCTCTGAAT[C/T]AGGAGATTTTAAATG	4297
rs538962176	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118442281	GGGAGGAATTTATTC[A/G]AGGATTGCTGGGATG	4297
rs539010445	snp	A/G	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118497001	TTTGTTTTTTTGAGC[A/G]GAGTTTCGCTCTTGT	4297
rs539023675	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118441701	TGGTTTATACTGAGC[A/G]TTAGAAATTCAGTCT	4297
rs539226576	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118457958	TCTCTGTTTTCATAC[C/T]GTAGCCTAGGAATGG	4297
rs539251803	snp	C/T	0	0	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118523888	CCCAACTCCATTGGG[C/T]CACTCCCCTCCTTCC	4297
rs539306268	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118497867	ATCTTCACTGGAAAA[A/G]CTAATGCCGAGGAAA	4297
rs539389451	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118507709	GTGGCTCACGCCTGT[A/G]ATCCTAGTAGTCTGG	4297
rs539451626	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118507064	CACTTTGGAAGGCTG[A/G]GGCAGAAGGATTGCT	4297
rs539469982	snp	A/C/G	1.6593e-05	0.00288031	intron-variant	KMT2A	GRCh38.p7	11:118496419	TACTCCAAAAGAACT[A/C/G]TTTGTCCTTGTGTCC	4297
rs539515636	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118496706	AGTTGCATATTAAAA[A/G]GCTTGTGTTTCATAT	4297
rs539529548	snp	A/C	1.64751e-05	0.00287007	synonymous-codon	KMT2A	GRCh38.p7	11:118505618	TGCTCCCTCTAGTAC[A/C]CCTTCAAACATTGCC	4297
rs539532382	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118451260	TCTTCCACCCAGGCT[A/G]GGATGCAGTGGCACA	4297
rs539575655	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118460894	AAATTGCACACTGCC[C/T]GTCTGCCTTAGATAC	4297
rs539596480	snp	C/T	4.94417e-05	0.00497176	missense	KMT2A	GRCh38.p7	11:118504392	ACTGAGCTCCTGAAA[C/T]CAGATTCAGACAATA	4297
rs539656885	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118514153	AAATCTTACTATTGC[C/T]TACTAGTTACAGAGT	4297
rs539696770	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118485424	AATTAGAAATAAATA[C/T]ATGTTGGGTGGCAGG	4297
rs539714014	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522791	CAAACATTGAGCCTG[C/T]AGGCTTTGAGTGGGA	4297
rs539736088	snp	A/G	0.00199481	0.0315187	intron-variant	KMT2A	GRCh38.p7	11:118477886	ATATTTTATTTTAAT[A/G]TATTTCATTTTTGGA	4297
rs539758748	snp	C/G			upstream-variant-2KB	KMT2A	GRCh38.p7	11:118436134	TCCTCGCCCCCTCCC[C/G]CTCTCTCCGGAACCC	4297
rs539802616	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118487073	CAAATATTCTCTTAG[C/T]CCCTATTACGAACAA	4297
rs539837639	snp	C/T	8.23635e-05	0.00641677	synonymous-codon, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521366	TGAGTATGCCGGCAA[C/T]GTCATCCGCTCCATC	4297
rs539841471	snp	A/G	1.70003e-05	0.00291545	missense	KMT2A	GRCh38.p7	11:118495709	TTTCAGCAGTGGGAT[A/G]TTACCAAACGCAGTG	4297
rs539862844	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118486590	TGGTAAAGAAAATCC[A/G]CGTCGGGTGCAGTGG	4297
rs539943476	snp	C/G	0.00279162	0.0372561	intron-variant	KMT2A	GRCh38.p7	11:118463698	TGGGCAAGTCATTTG[C/G]CCTTTTAGAGCTTCA	4297
rs539955212	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118438623	TCCTGGGCAAACCCC[A/T]TGTCCCCTATTGTGC	4297
rs539992728	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118474637	TAAGGTTGGGACTAT[A/G]TCACAGAGGATGCTG	4297
rs540001108	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118441962	ATTGCCTCCCTTACC[C/T]TGTGGCTAGAGGGGG	4297
rs540017928	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118448251	ATTTGTAGCTTTTAT[A/G]TCCATTTTCAGTTGT	4297
rs540066359	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118456542	ATGGGGTTTCACTAT[A/G]TTGGCCAGGCTGGTC	4297
rs540080099	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118447530	TGGGGTTTTGAAAGC[A/G]ATGTTAGGGTATCCT	4297
rs540130684	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118466687	AGGTGTGGTGGCACA[C/T]GCCTGTAATTCCAGC	4297
rs540182052	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118491950	CAAGTCTCATTTTTT[G/T]CTGAGAGCTTGTTCT	4297
rs540193148	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118454969	TGTCTACCCTAGCGA[A/G]TATAACCCCACAGCT	4297
rs540202663	snp	A/C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118445969	AGATTCCGCCACTAC[A/C/G]CTCCAGCCTGGGCGA	4297
rs540237246	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118435195	CCAGCCTCAGCCAAC[C/G]CAAGTTCTCCCGACA	4297
rs540265747	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118444624	TTTGTTGCCTAGGCT[A/G]GAGTGTAATGGCACA	4297
rs540275607	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118500311	ATCCACACAATAATG[A/T]TCAAATTTTTCAATA	4297
rs540287276	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118471171	GACTCTGAGCTGCCC[A/G]AGGAGTTGGTATGTT	4297
rs540331743	in-del	-/T	0.00199481	0.0315187	intron-variant	KMT2A	GRCh38.p7	11:118456505	ACCACGCCCAGCTAA[-/T]TTTTTTGTGTTTTTA	4297
rs540332959	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118443817	ACCAGTGGGCAGCAT[A/C]GGTCCAGTAGCATTT	4297
rs540394733	snp	C/G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118452473	GGAATAGGAGGCTGC[C/G/T]GTGAGGTATGATCAT	4297
rs540421954	snp	C/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118515446	AGAGGTAGGGACAGA[C/T]GTGTCAGGATTGATT	4297
rs540438266	snp	C/T	1.64746e-05	0.00287002	missense, intron-variant	KMT2A	GRCh38.p7	11:118473921	TTGTTGGTGAAGATG[C/T]TGCCACTTCATCTTC	4297
rs540461485	snp	A/C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118464115	CTGTAGTAGCAGACT[A/C/G]TCCAGTTTGCAAGGA	4297
rs540824392	snp	A/G	0.00119737	0.0244387	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118518849	TTGGAAGGCCAAGGC[A/G]GGTGGATCACGAGGT	4297
rs540885998	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118518072	TGTGCAATTGCAGTC[C/T]TAATACAATTACACT	4297
rs540886080	snp	C/T	9.8868e-05	0.00703024	missense	KMT2A	GRCh38.p7	11:118503453	CAGGCACCACGGAAA[C/T]GCACAGTCAAAGTGA	4297
rs540914931	snp	C/G	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118460689	TAGAGACAGGATCTG[C/G]CTATGTTGCTCAGGC	4297
rs540949555	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118458213	CTCAACCTCCCAAGT[A/G]GCTGGGACTACAGGC	4297
rs540995018	snp	G/T	0.00119737	0.0244387	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118516555	TGGGAATATCTTTGA[G/T]GTGTTTATTGTCTGT	4297
rs540999292	snp	A/G	3.29468e-05	0.00405861	synonymous-codon	KMT2A	GRCh38.p7	11:118506359	CAACTTTACCCAGAC[A/G]GTAGACGCTCCTAAT	4297
rs541009116	snp	C/T	3.29625e-05	0.00405958	missense, intron-variant	KMT2A	GRCh38.p7	11:118474044	AAACCAAAATACTTA[C/T]AAAGAAAGGGAGAGG	4297
rs541026115	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118525537	CCAGCCCGCCACCCT[A/G]CTCGCCTCCGTCAAA	4297
rs541047410	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118480574	TAACTGCAGGAAACT[A/G]AGAATGTTGTGTCAC	4297
rs541132022	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118492215	CAGTAACCTGATCAG[A/T]GTTGCTTCTTAGAAA	4297
rs541173759	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118488371	TAGCATGTTCTGTTA[A/T]ATCTTGTATTATATT	4297
rs541230473	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118497344	AACTGGCTTTGAAAT[A/G]CAGTTTATAGATGTC	4297
rs541254946	snp	A/C	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118441956	ATACCAATTGCCTCC[A/C]TTACCCTGTGGCTAG	4297
rs541288439	snp	A/G	0.00318978	0.0398085	intron-variant	KMT2A	GRCh38.p7	11:118452436	CCTCAGGAGACTGAG[A/G]TGGGAGCATCACTTA	4297
rs541289679	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118507248	GGCTAAATGATCCAT[A/G]GTCATGTCACTGCAC	4297
rs541351408	in-del	-/T			intron-variant	KMT2A	GRCh38.p7	11:118448963	TCAGAAAACAAGAGA[-/T]TGTAAAATTCATAAA	4297
rs541395734	snp	A/C	0	0	intron-variant	KMT2A	GRCh38.p7	11:118459291	CAGGCTGATCTTGAA[A/C]TCTGGCCTCAAGTGA	4297
rs541395847	snp	A/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118450024	TAATTTTTCTAGCCT[A/T]TTCAAATCAATCTGG	4297
rs541431062	snp	A/C	3.36542e-05	0.00410195	missense	KMT2A	GRCh38.p7	11:118494696	TGTTTTCTTTTAGCA[A/C]ATGGAACGTGTTTTT	4297
rs541457206	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118458254	CCCAGTTAATTTTTT[C/T]TATTTTTTATAGAAA	4297
rs541457481	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118448520	AAAACTTGAATTGGG[A/T]TTATTCATATAGATT	4297
rs541497025	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118468525	TATCCTCTGTGTACT[A/G]TGCACCAAAGATGAC	4297
rs541497419	snp	A/G	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118438085	GGGCTTGGAAGGGGT[A/G]GGGGAAGCCAGGTTG	4297
rs541584165	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118455759	CTGGAGTTCAGTGGC[A/G]CAATCATGGCTCACT	4297
rs541622963	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118486024	GGAGGTGGAGCTTGC[A/G]GTGAGCCGAGATCGC	4297
rs541643752	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118455211	TGTCTTTTATTTATT[A/T]GTTATATGTTTATTT	4297
rs541756890	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118483173	GCGAGGCGGAGGCTG[C/T]AGTGAGCCGAGATTG	4297
rs541783879	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118439165	TACAGCAGCAAAAAA[A/G]AAAAAAAAGAAAAAA	4297
rs541803521	snp	A/G	0.00199481	0.0315187	intron-variant	KMT2A	GRCh38.p7	11:118475520	CGAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA	4297
rs541880219	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118514490	CTGTCACCCAGGCTG[C/G]AGTGCAGTGGCGTGA	4297
rs542026586	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118436184	CGGGCTTCCTTCCCC[C/G]CTCCTTTTCCCGAGC	4297
rs542027269	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118466060	GATAATTTTTTTATT[C/T]TAAAATTACTTTTAG	4297
rs542065416	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118501206	CTCACGCCTGTAATC[A/G]CAGCACTTTGGGAGG	4297
rs542107417	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521518	TGTATGTTATCAATT[C/T]AGAGACCTTTCTTAA	4297
rs542128754	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118511584	CTGCTTAAATCATTA[C/T]TACTAGTGCTGTTTT	4297
rs542151074	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520496	TCTCTACTAAAAATA[C/T]AAAAATTAGCCCGGC	4297
rs542250159	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118484667	ATATTCAATATGAAT[G/T]GAACAACTAGGTGAG	4297
rs542311386	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118493316	ACTGAGTATAAGTAA[A/G]TTTAAAAATGAATTG	4297
rs542334625	in-del	-/CGTCTCTCGGG			intron-variant	KMT2A	GRCh38.p7	11:118437379	AGTTTTCCTCTCGGG[-/CGTCTCTCGGG]TGATGGCCTCATCCA	4297
rs542339031	snp	C/T	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118502143	CTGTAATCCCAGCTA[C/T]CCAGGAGGCTAAGGC	4297
rs542341518	snp	A/C/G	3.30985e-05	0.00406797	missense, intron-variant	KMT2A	GRCh38.p7	11:118473648	AGCCATTTTCATCAA[A/C/G]TAGTCCTACTCCTCT	4297
rs542504480	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118444905	CCTCTCCATACCTCT[G/T]TTTCTTCATTTGTAA	4297
rs542536164	snp	C/T	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118453970	ACATGTAAGATTTAT[C/T]GTCGATTTATCTCTT	4297
rs542602341	snp	C/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118453371	AAACCCTTTGGCAGC[C/G]TTTGAACCAGCTGAC	4297
rs542602403	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118463622	TGTATCTATTATGGT[A/G]GGAAAACTATTCTAC	4297
rs542630628	in-del	-/CCAGCAGTTCAAGA	0.0170251	0.090679	intron-variant	KMT2A	GRCh38.p7	11:118482697	GAGGATTGCTTGAGG[-/CCAGCAGTTCAAGA]CCAGCAGTTCAAGAC	4297
rs542680888	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118510617	TTCTCTCATAGCTTA[C/T]ATTTTGTTTTGTCCG	4297
rs542693464	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118452382	TCTACAACAGAATAA[A/G]AATAACCAGGCATGG	4297
rs542752721	snp	A/G	4.95864e-05	0.00497903	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118472500	ATTAGAGTCTACACC[A/G]AATAGTAGATTCAGT	4297
rs542807054	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118502062	GTTCAAGACCAGCCT[A/G]GCCAACATGGTGAAA	4297
rs542811833	snp	C/T	1.65302e-05	0.00287486	synonymous-codon	KMT2A	GRCh38.p7	11:118481761	CAGTGAAAAGAAAGA[C/T]AGCAAAGAGAGCAGT	4297
rs542835580	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118470642	TTAGAAAGCTCAACA[A/G]TAAAACCTTTGTTGA	4297
rs542835900	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118459667	TATGGTATATTGAAA[A/C]TAATTTTTTTTTTTT	4297
rs542897156	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118469803	GGGTCTCACTTAAGA[A/G]TCATCATATATTATC	4297
rs542928942	snp	C/T	3.30006e-05	0.00406192	intron-variant	KMT2A	GRCh38.p7	11:118480274	TTCCCCCAAATGCTC[C/T]TTGCTTAAATGGTGT	4297
rs542952116	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118497876	GGAAAAGCTAATGCC[A/G]AGGAAAACCTCCTTT	4297
rs542969287	snp	A/G	0.00199481	0.0315187	intron-variant	KMT2A	GRCh38.p7	11:118452142	GAAATCCTGAGCTTA[A/G]GCGATTCTACTCCCT	4297
rs543061127	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118508089	AACAAGAATTATTTA[A/T]ATAATGGATAATAGT	4297
rs543107992	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118451851	TAAGTATTCACATTT[C/T]TAATACTTTGCAAGA	4297
rs543119165	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118487501	AGAGAATTCTAAGTA[C/T]CCCTCACCCAAATTC	4297
rs543122404	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118517905	TTTGTTTGTTTTTGA[A/G]ATGAGGTCTCACTCT	4297
rs543161921	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118441882	TCCCATCTTGACTTA[A/G]TTCTCATCTCTTTGC	4297
rs543220529	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118526982	CCCACCTTCAGGTCC[A/C]CTCCACACTGGCTCT	4297
rs543283835	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118526099	ACAGTTGCTAGTAGC[C/G]GCAGGAAGATGTCAG	4297
rs543313228	snp	A/G	0.00279162	0.0372561	intron-variant	KMT2A	GRCh38.p7	11:118464768	TAATGGCTACCAGGA[A/G]GTAGAAGTGGTCCAG	4297
rs543336095	snp	A/G	0.00199481	0.0315187	intron-variant	KMT2A	GRCh38.p7	11:118440381	CCCTCTGTAGTGTCA[A/G]TATCCCATTTTTCTA	4297
rs543351675	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118448850	GAAGGGCAGTTTGAC[C/T]CCTTAATTATAAAGT	4297
rs543408828	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118488172	GCGACAGCGAGACTC[C/T]GTCTCAAAAAAATAA	4297
rs543509419	snp	A/G	0.00199481	0.0315187	intron-variant	KMT2A	GRCh38.p7	11:118497295	GGCGTGAGCCACCGT[A/G]CCCGGCCAAAAGCTT	4297
rs543535134	in-del	-/T	0.00517822	0.0506191	intron-variant	KMT2A	GRCh38.p7	11:118480321	AGTAGAAGAGAATAC[-/T]TTTTTTTTTAAAGTA	4297
rs543572659	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118507126	ACATAGTAAGACCCT[C/G]TCTCTACAAAAAATT	4297
rs543633398	snp	A/G			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118523004	GCATAGGATGTGCCT[A/G]CAAAAAGTTCCCTGA	4297
rs543638379	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118449933	AATGAAGTTAACCAC[C/T]TAAACTTGTCATATG	4297
rs543656966	snp	A/T	0.00279162	0.0372561	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118515631	AGGCTTAGGAACAAA[A/T]GGACATCTCACAGAC	4297
rs543672906	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118494561	AACTTGGTGAGGTTG[C/T]CAGAGTGGATGGATC	4297
rs543699715	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118494534	AATTTGATCCCCTGA[G/T]TCTTTGAGAGGAACT	4297
rs543713821	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118524133	TTTCCCTCTGCCCAC[A/C]AAGTCCTCATATCTG	4297
rs543733077	snp	A/G	4.95552e-05	0.00497747	missense	KMT2A	GRCh38.p7	11:118503120	TTGAAGCTATCTGGA[A/G]TGAGCAACAGATCAT	4297
rs543760853	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118447491	ACAGGTGCCATGATG[C/T]GACATTTTTGTAAAG	4297
rs543797601	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118502341	CATTGAAACCAGTGA[C/T]TTCTACACATTTGTT	4297
rs543801142	snp	A/G	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118457185	TAGCCTTCAGGATGA[A/G]GTCTACACGTCCTCA	4297
rs543801172	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118468298	AGGAACTGACAATTA[C/T]GGCACTTTCAGTCTC	4297
rs543853325	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118461791	TATTACTGTAGTCTT[G/T]TGATTTCTAGATAAG	4297
rs543885239	snp	A/G	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118477074	GGCTCTTCATAGTTA[A/G]TAGGTCCTCTGAAAA	4297
rs543929068	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512565	ATTTGGGTTTTTTCT[A/G]TTTTCTGCTACGAAT	4297
rs543935101	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118486637	CAGTACTTTGGGAGG[C/T]TGACGCAGGAGGACC	4297
rs543984671	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521484	GACCAGTATGACCCC[C/T]GGATCACAAAAGAAA	4297
rs543999430	in-del	-/T			intron-variant	KMT2A	GRCh38.p7	11:118468008	AGGTTAAACAAATCC[-/T]TTTTTTTTTTATAGA	4297
rs544026901	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118464004	AAGAATGGTGAAATC[A/G]TTGATGCTTTACATA	4297
rs544131318	snp	A/G	0.0023933	0.0345097	intron-variant	KMT2A	GRCh38.p7	11:118437834	GCTTAGAGAAGAGCA[A/G]CTTTCCACCACTCCC	4297
rs544135781	snp	C/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520448	ATGAGGTCAGGAGTT[C/T]GAGACCAGCCTGACC	4297
rs544160747	snp	A/G	0.00812208	0.0632066	intron-variant	KMT2A	GRCh38.p7	11:118447633	TTTCTAGGTTCCTCA[A/G]CTTAAAAGGGATGAG	4297
rs544198726	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118437517	ATACTGCCAGCCACT[A/C]CCCCTTCCTTCACCT	4297
rs544219331	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118483772	TGTGGTGGCTCACAT[C/T]TATAATCCCAGCACT	4297
rs544241674	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118436107	CTCCCTACGCCTCCA[A/T]CCTCCGCGTAGTCCT	4297
rs544251228	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522281	TGCGTGGCACAGCTG[A/T]GGGGCCTCTGTGATG	4297
rs544281191	snp	C/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118492554	CATGGTAGCGGTCAC[C/G]TGTAGTCCCAGCTAC	4297
rs544303559	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118435219	CCCGACACAAACCCC[C/T]CCCTACCCTCTCGGC	4297
rs544470638	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118484646	ATCCCAGTGTATTTT[C/T]GCAATATATTCAATA	4297
rs544658551	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118492093	GACCTTCTTTAGCGT[A/G]AGAAATAGGAAGGAG	4297
rs544695055	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118445748	TGGCTCACGCCTATA[A/G]TCCCAGCACTTTGGG	4297
rs544744890	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118511499	GGTTAGAGCTGGAAG[A/G]AACTGTAAGGATTTT	4297
rs544750320	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118443313	GACTTCCCATAAAAT[A/G]GTTCTTTATGTTTTT	4297
rs544808283	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118510445	CTCTCCCTTGTGTGC[C/G]TTCACACGTGCTTTC	4297
rs544814728	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118499169	CTTTTGGGAAATACA[A/G]AAGTGTCCTGCTAAG	4297
rs544824783	snp	A/G	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118490302	TGTACTTGGTGTTCT[A/G]GAGGTGAACTAGACT	4297
rs544856400	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118465065	TCAGTATCATTAAGT[A/G]TGCTGATTTGTCTCC	4297
rs544878736	snp	A/C	0.0023933	0.0345097	intron-variant	KMT2A	GRCh38.p7	11:118452655	TGTTTTTTTTTTGAG[A/C]TGGAGTCTCACTCTG	4297
rs544907816	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118518904	AACATGGTGAAACTC[C/T]GTCTCTACTAAAAAT	4297
rs544908934	snp	C/T	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118462752	TTTTTTTAGTAGAGA[C/T]AGGGTTTCACCGTGT	4297
rs544940569	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118461930	TGCAGTGAAAGGAGG[A/T]CTTTTTTGCAGCACC	4297
rs544991942	snp	C/T	0.0023933	0.0345097	intron-variant	KMT2A	GRCh38.p7	11:118507437	TAGACTTTATCAGAT[C/T]CTGATAGAGCCATTT	4297
rs544992374	snp	A/C	0.00438332	0.0466095	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118517805	TGATCATGCTACTGC[A/C]CTCCAGCCTGGGCAA	4297
rs545037599	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118451731	TCCCAGGCTCAAGCA[A/G]TCGTCCTGCCTTGAC	4297
rs545067358	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118497742	AGTTTCAGTCTATGG[A/T]AAAAGTAATCTTGAA	4297
rs545083619	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118518923	TCTACTAAAAATACG[A/G]AAAAAATTAGCCAGG	4297
rs545098406	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118460405	GGATCCTCCTACCTC[A/T]GCCTCCCGAGTAGCT	4297
rs545137424	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118449395	AGACCTGATCTCTAC[A/C]AAATAAAAATTTTAA	4297
rs545159100	snp	C/G/T	3.29717e-05	0.00406015	missense	KMT2A	GRCh38.p7	11:118504336	GCCGCAGAGTCCACA[C/G/T]AAGTACCCCCTCCGA	4297
rs545161512	snp	A/G	0.00199481	0.0315187	intron-variant	KMT2A	GRCh38.p7	11:118480604	CATTTCTACGCTTCT[A/G]TTTTTTAAATGTATT	4297
rs545209935	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118468660	GGAATGATGATAATT[A/C]ATATATAAAGGCAAC	4297
rs545252424	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118498283	AATTGTAGGAACTGT[A/G]GAATGGGATGAGTCT	4297
rs545273174	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118478382	ATACTCTGGGGCCAT[A/G]CTGTCATTAATAGAA	4297
rs545276311	snp	C/T	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118495261	CCTCCCTGGTTCAAG[C/T]GATTCTCCTCCCTCA	4297
rs545388306	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118441983	CTAGAGGGGGTGGCA[A/G]CAGTGCTTTGCTTGC	4297
rs545411349	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118451141	TTTATACTCTAGGTG[A/G]ATGACCAGCTACTGG	4297
rs545432427	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118440812	TTTTAATGTTTACTG[A/G]TCATGTATGTACCAA	4297
rs545471644	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118459433	AGCTGCTAAAGGGCA[C/T]GTTTGAGATGCCTAC	4297
rs545493967	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118486845	GTGAGCCATTATCAC[A/G]CCACTGCACTCCAGC	4297
rs545494394	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118439346	ATTTTCTTCTTGTTC[A/T]GTATGCTTATTTATT	4297
rs545499730	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118525668	AAAAAAATATTCTAA[C/T]GAATGTATCTTTCTA	4297
rs545555084	snp	C/T	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118495455	AGCCACCATGCCCGG[C/T]CTCTTTTGAGTTTTT	4297
rs545561953	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118448750	ATATAATGAATGGTC[C/T]CTACTTTTAACCAGT	4297
rs545584537	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118437216	TGGCACAGACCCCCT[C/T]GCCGGGGTTTCCCAT	4297
rs545610880	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118485772	GTCCATCTATAGGGA[A/G]CATGGGTTAAAATAA	4297
rs545692866	in-del	-/T	0.00914312	0.0669923	intron-variant	KMT2A	GRCh38.p7	11:118445884	GGTTGCGCACCTGTA[-/T]CCCCAGCTACTCGGG	4297
rs545715501	in-del	-/A	0.00279162	0.0372561	intron-variant	KMT2A	GRCh38.p7	11:118492872	TAAGTTACCCTAGCT[-/A]AAGCTATTACATAAC	4297
rs545732630	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118487423	AAACTCTCCTCCATG[C/T]GAATTTTTTAAACTT	4297
rs545808942	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118440908	AGGGAACACAAGCAG[A/G]GTGGAGTGCACGAAG	4297
rs545831095	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118466201	GCTGAGTGCTGGTAC[A/C]TGCCTGTAGTCCCAG	4297
rs545956369	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118515478	GTACAGGAGCTTGCA[A/G]TGTCATCAAATACCT	4297
rs546008256	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118456842	ATTCAGATGTCTAAA[A/G]TGATCTCTCTTCCCA	4297
rs546017786	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118514624	TTTTGTATTATTATT[A/T]TTTTTTTATTTTTAT	4297
rs546038469	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118523137	ACATATGTAGCATGA[G/T]TTTGTAGGAGAGGAA	4297
rs546071196	snp	A/G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118467060	TTCCTTAAATTTAGG[A/G/T]TTCATACATTCTTAG	4297
rs546124912	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512502	TTGCCAAATATTCCA[C/T]TGTGTAGATATACCA	4297
rs546249146	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118510714	ATTCATCTTTGTATC[A/G]CAAGCATCTAAGTGT	4297
rs546304451	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118509815	TCTTGGGTTTGTTAT[C/T]TATAAATGGGAATAA	4297
rs546304738	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118485610	TGGAAATATATATCT[A/G]TCTTTAAAATAGGTA	4297
rs546326399	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118494510	GTGTGTATAAAACAT[C/T]TTTGGTTTAATTTGA	4297
rs546358109	snp	C/T			upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118525557	CCTCCGTCAAACCCC[C/T]GGCCAATGCAGTGAG	4297
rs546477598	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118436337	CGAGGCCGCTATACA[A/G]ATTGCGGGGCTGGCG	4297
rs546491675	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118462220	CTACCTTCCAAAGTG[C/T]TGGGATTACAGGTGT	4297
rs546510417	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118501301	CATCTCTACTAAAAA[C/T]ACAAAAAAATTAGCC	4297
rs546537348	snp	A/T	1.6516e-05	0.00287362	missense	KMT2A	GRCh38.p7	11:118481832	CATCAGCAAGAGAGG[A/T]TCCTGCCCCAAAGAA	4297
rs546599012	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118480819	AGGTGCGCACCACCA[C/T]GCCCAGCTAATTTTT	4297
rs546620460	snp	A/G			intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118511860	TGTTCACACTGTAGG[A/G]ATTCTAAGCAGTGCT	4297
rs546635239	snp	C/T	6.59554e-05	0.00574224	synonymous-codon	KMT2A	GRCh38.p7	11:118499878	TCTAAATGATCTCTC[C/T]GACTGTGAAGATAAG	4297
rs546661939	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118489634	GAAATAAATCTATCT[C/T]AATGCTTTAATTGGG	4297
rs546677558	snp	C/T	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118487762	TACTATTATCTGATC[C/T]ATAGGCCTTATTTAG	4297
rs546755581	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118442999	TTTTTGTTGTTGTTA[C/T]TGTCATTTCATTGGT	4297
rs546768408	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118452867	TCGAACTCCTGACCT[C/T]GTGATCTGCCCACCT	4297
rs546816222	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118498736	GACACATGGTTATCA[C/T]CCTGACTCCTGTAGT	4297
rs546851915	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118455096	GCAGTGGCTCAGTCA[A/G]TTCACTGCAGCCTCA	4297
rs546852883	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118507259	CCATGGTCATGTCAC[G/T]GCACTCCAGCCTAGG	4297
rs546877630	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118508285	ACTGTTCTGTATTTG[G/T]TTTTTCACTTATGTA	4297
rs546882342	snp	A/G	0.00358779	0.0422022	intron-variant	KMT2A	GRCh38.p7	11:118451347	CTCCTGAGTAGCTGG[A/G]ACCATAGGCTCACAA	4297
rs546912129	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118471129	AAACTTTCTTAGTCT[A/G]CTTTGGCAAAACAGA	4297
rs546945595	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118450394	GGTCACCTGTCTCAT[C/T]TGCTTTGCTGTTTTC	4297
rs547034973	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118459775	CCCTCCCAACCCCCC[A/G]CCCCGGGTTCAAGCA	4297
rs547094206	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118469933	TGTGCTATTCAGACA[A/G]TAGCAGTGTTCTCTT	4297
rs547129080	snp	A/G	0.0023933	0.0345097	intron-variant	KMT2A	GRCh38.p7	11:118442723	CTTGTAGGCTCCACT[A/G]TTTCTTGAGATTTTC	4297
rs547233290	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118507687	TAGTTCTTCCAGGCC[A/G]GGCGCAGTGGCTCAC	4297
rs547387693	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118458802	CAAAGGGGAAGTGGT[A/G]TTCTTTTTAAACTTA	4297
rs547448531	snp	A/G	0.00279162	0.0372561	intron-variant	KMT2A	GRCh38.p7	11:118469115	CATCTAGCATTAGGT[A/G]TATCTCCCAATGCTA	4297
rs547463710	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118524846	GACCTAGTTACTGCC[C/T]TGCTAGGCCATGCTG	4297
rs547505104	snp	C/G	0.00119737	0.0244387	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118523269	CTTGTTAAGACATAG[C/G]AAGACTTAATTTTTA	4297
rs547507729	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118496389	ACTTTGCAACACAGG[A/G]CCCTAGTTAATACAT	4297
rs547567552	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522729	AGACAGGATTCCTAG[C/T]ACCTCCGGTGTCAAA	4297
rs547617104	snp	A/T	0.00398564	0.0444627	intron-variant	KMT2A	GRCh38.p7	11:118454855	AATTTTTTTTTTTTT[A/T]AATTTTAACTTGCAG	4297
rs547622667	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118487642	GTTGCAGACATAAAC[A/C]ATTTTACCTCTAAAT	4297
rs547687222	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118486981	CAAACTAGCTAAGAA[A/G]GTCAACCCTGCCCAC	4297
rs547705864	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118495588	TGACTTGTTCTTATA[A/T]TCTGTGAATGGCTCC	4297
rs547734820	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118439939	ACTTTTTTTTTTTTT[C/T]TAACATAGCCTTACT	4297
rs547751003	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118491024	GAGTATTCGAGGGGC[C/T]CAGAATAATCTTGAG	4297
rs547753576	in-del	-/A	0.00358779	0.0422022	upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118526737	AGTGTACATAGTTGT[-/A]AAAAAAAAGGAGTTT	4297
rs547769395	snp	C/T	0.000399281	0.0141238	missense	KMT2A	GRCh38.p7	11:118505494	ATCCCCAACTTTTGG[C/T]TTCAGAATCCAGCCA	4297
rs547790601	snp	C/G	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118485057	ATAGTCTGTTTTGTT[C/G]GTATTTAGCAGGTAC	4297
rs547814904	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118484568	AGAGGAAGTAATTCC[C/T]TCACATGGAAAGTAT	4297
rs547840041	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118449016	ACGGGATTATAAAAG[C/G]AAAGACAAATTGTCT	4297
rs547903505	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118448238	GAAACAAATAAGTAT[G/T]TGTAGCTTTTATGTC	4297
rs547937773	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118444655	AACATTTCATTTCAG[C/T]CTCAACCTCCAGGGC	4297
rs547988693	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118466534	AAGTAAAAAGAACTG[G/T]CTGGGCACAGTGGCT	4297
rs548049533	snp	G/T	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118476545	TATGTTGCCCATACT[G/T]GTCTTGAACTCCTGG	4297
rs548053958	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118478576	GTAACTAGTGGCTAC[C/T]ATATCAGACTGTAGC	4297
rs548064252	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118454489	TAACCAGGTTTGGCA[A/G]GTTTTTTTCTGCAAA	4297
rs548078066	snp	C/T	1.64738e-05	0.00286995	synonymous-codon	KMT2A	GRCh38.p7	11:118501769	TGGCTCCTGTTATTA[C/T]CATGTCATCTCAAAG	4297
rs548175500	snp	C/T			upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118525955	ACTTGCAACTTTTTG[C/T]TTGTTTTGGTTTTCA	4297
rs548180145	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118474759	ATAGAATAGAAAACC[A/G]GAGGGGAGCATTCTC	4297
rs548265332	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118437654	CTGAAGATAACGGTG[A/G]TTCCTCATACAGCAG	4297
rs548324745	snp	C/T	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118447137	CTAGTTGAAACTGAA[C/T]TTCTTTCCTGTTTTC	4297
rs548373987	snp	A/C	0.00015738	0.00886934	intron-variant	KMT2A	GRCh38.p7	11:118474330	GGTACTCTTTTCCAC[A/C]TTGCCTATTAAAACT	4297
rs548435224	in-del	-/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118517023	ATGTTTTTCAATGTC[-/T]TTTTTTTTTAACCTA	4297
rs548495196	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118508737	AAAAAAAAAAAAAAA[-/A]GGTGAAAATTGATTG	4297
rs548528154	snp	C/G/T	6.64413e-05	0.00576343	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520776	TTCCTGAAAAAAATT[C/G/T]GTTAATAGTATGTCT	4297
rs548584814	snp	A/G	1.69284e-05	0.00290928	synonymous-codon, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520044	TGAAGAAGAGGAGGA[A/G]GTACAGCTGAAGTCA	4297
rs548659944	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118443899	CATTTCTGGTTTTGT[A/G]TTTTGTTGGGATGTT	4297
rs548698736	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118509511	CTTCACTTTTTAGTT[A/G]TTACTAAAGAAAACT	4297
rs548801652	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118435354	CCTTCTTTCCCCCTC[C/T]CCCCTCAGCTTACTA	4297
rs548868778	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118491401	TTTAAACCTAAAATT[A/G]TGGTTGTGTTGTTAT	4297
rs549019207	snp	C/T	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118452790	AGGCGCCCACCACCA[C/T]GCCCTGCTAATTTTT	4297
rs549070729	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118459832	GCTAGGATTACAGGC[A/G]GGCACTACCACGCCC	4297
rs549086164	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118518507	TGAGGCTGGCTGGGT[G/T]CTGTGGCTCACACCT	4297
rs549133042	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118445776	GGGAGGCCAAGGCGG[A/G]AAGATTGCCTGAGGT	4297
rs549240414	snp	A/G	0.000513075	0.0160086	intron-variant	KMT2A	GRCh38.p7	11:118495916	ACCAAAAGGAGAGTC[A/G]TCACCCATTTCCCTC	4297
rs549240640	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118446486	GGCTAGTAAGTGGCA[A/G]GGCTAGAATTTAAAT	4297
rs549272028	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118451184	GGAGACGTCCCTTCC[C/T]TCATGAAACTTGCTA	4297
rs549290735	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118437866	TTGGAGAGGAGGCAG[C/G]CTTTCCCTCCAGCTC	4297
rs549290766	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118479839	TTACTTGATGGATAT[C/T]AACATCGTAAGAGAG	4297
rs549310201	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118457778	GTTTTCATCCTCTCT[G/T]CAATGGCCTTCCCGA	4297
rs549312102	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118469020	TTATACTTTAAGTTT[C/T]AGGGTACATGTGCAC	4297
rs549344499	in-del	-/A	0.0023933	0.0345097	intron-variant	KMT2A	GRCh38.p7	11:118499623	AACCCTGTCTCTACT[-/A]AAAAAAATTAGCTGG	4297
rs549374911	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118467746	TGTGTTCTTACCTCT[C/T]GAGAGGAAAATGTTA	4297
rs549490812	in-del	-/AG	0.0107246	0.0724382	intron-variant	KMT2A	GRCh38.p7	11:118509303	ATTTAAAAAAAAAAA[-/AG]TCTAAGCTCCAAAGA	4297
rs549556140	in-del	-/A	0.00795532	0.062565	intron-variant	KMT2A	GRCh38.p7	11:118449748	CCTTTAGAAAGAAGG[-/A]AAGTTGTGGATTCCT	4297
rs549572838	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118450233	TTTTTTTTAAAGATT[C/T]TGCAGAATAATTTGG	4297
rs549611729	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118516117	CAAAACCTGTCCATT[A/C]TACTCCATTTCCAGT	4297
rs549877223	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118486907	AAATTTTTAAAAATT[A/T]AAAAAATAAGAAAAT	4297
rs549948307	snp	A/C	0.00199481	0.0315187	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512889	TTGGTATTAGACTTC[A/C]TATTAAATTTAGGCA	4297
rs549993458	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118455479	TCTACATTTGAGAAC[C/T]AATGGTAGCAGTCTG	4297
rs550009614	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521653	AGTATCAGAAGCAAA[C/T]AGCTATACAAGTTTT	4297
rs550055377	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118495003	TAATTGTGACAAATG[C/T]ACAATACATGTGTGG	4297
rs550109490	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118448120	GAAGTAATGGTTTTT[C/G]TAGTGGCTTTATAGG	4297
rs550127841	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118513950	CTCAAAAAAAAAAAA[A/G]AAAAAAAAGAAAAAG	4297
rs550155463	snp	A/C	0.00676609	0.0577691	intron-variant	KMT2A	GRCh38.p7	11:118486005	GGAGAACGGCATGAA[A/C]CCGGGAGGTGGAGCT	4297
rs550172932	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118456239	GCATGGTGGCTAACA[A/C]CTGTAATCCCAGCAC	4297
rs550188805	snp	A/T	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522637	AGCCAGGCCCCACCT[A/T]CAGCGTCTGTCGAAC	4297
rs550216966	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118501425	AGTCAGCCAAGATCA[C/T]GCCACTGCCCTCCAG	4297
rs550235275	snp	C/T	0.00013185	0.00811835	missense	KMT2A	GRCh38.p7	11:118484196	AGGAAAAACCACCTC[C/T]GGTCAATAAGCAGGA	4297
rs550298010	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118492743	AAGCTGCTGTTTTAT[C/T]TTTTAATAGAGCTCC	4297
rs550341707	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118511001	TGGCATTGAAATCCA[C/T]GTGAGGTAATAGTGA	4297
rs550403686	snp	C/T			upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118525920	AATCATGAATACTAG[C/T]CAAGTCACACACTCT	4297
rs550409787	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118480029	AGGCTCAGATTTAAT[C/T]TGAGTAATGAGCAGT	4297
rs550431566	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118516460	ACACAGTGAAACTCT[C/T]TTAAAAAAAATTAAA	4297
rs550448107	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118462953	GAAAGTACTTAGAAA[C/G]TTTAAATATTGGCAG	4297
rs550464573	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118456034	TTTTTTAGACAAGTC[A/T]TCTCCCTTTGTTGCC	4297
rs550508140	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118462567	ATTTTTATTTATTTA[C/T]TTATTTTTTGAGACA	4297
rs550630027	snp	A/G	0.00438332	0.0466095	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118436440	GTTCCGGGGCCCCGT[A/G]CCCCCCCCTCCGCCT	4297
rs550647979	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118446115	ACACTTTGGAAGGCC[A/G]AGGCAGGCAGATCAC	4297
rs550710755	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118454376	TGTCTGTCATGCATG[C/T]TGTGCCTGTTGCTGT	4297
rs550728480	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118434535	ATCCACGTGGTCGCC[A/C]ATCTGTAACTGATCA	4297
rs550762734	snp	A/C/G	9.83731e-05	0.00701275	intron-variant	KMT2A	GRCh38.p7	11:118482130	AATTGCTGAACCACA[A/C/G]GTACTAACAAAAAAG	4297
rs550821530	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118466948	TATGTAGTCCGAGCT[A/G]TGCAGGAGGCTGAGG	4297
rs550853346	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118443184	TGGCTGAGGTAGATT[A/G]TGCTGGGAATAGGGA	4297
rs550854430	snp	A/G	0.0182019	0.0936463	intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118519093	AAAAAAAAAAAAAAA[A/G]AAAAAAGAAAATTAA	4297
rs550920870	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118442331	TATGTTATTTTCAGG[A/G]ATTAAGAAAGGTTAA	4297
rs550954564	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118482970	AGGCGCAGCGGCTCA[C/T]GCCTGTGATCCCAGC	4297
rs551050942	snp	A/G	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118452105	GCTGTTCACAGGCAT[A/G]ATCATCATGTATTAC	4297
rs551065396	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118518162	TACCAAACCAGTATT[C/T]GTAAATGAAATAATA	4297
rs551114304	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118461037	TGAAAAGTTGTCTTA[A/G]TAGTACATAATTCCT	4297
rs551128730	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, downstream-variant-500B, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118527158	GATTTTTATCGGTTT[C/T]CTCAACTGTGAATAT	4297
rs551144488	snp	A/G	6.59652e-05	0.00574267	missense	KMT2A	GRCh38.p7	11:118489817	AGTGTAATAAGTGCC[A/G]AAACAGCTATCACCC	4297
rs551185278	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118499679	CAGCTACTTGGGAGG[C/G]TGAGGCACAGGAATC	4297
rs551247010	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118498969	AGTTTCACATAGTTG[A/G]AATCATATAGTACAT	4297
rs551309958	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118508544	GAGTTTGAAACCAAC[C/T]TTGGCAACATAGGGA	4297
rs551350623	snp	C/T			upstream-variant-2KB	KMT2A	GRCh38.p7	11:118434921	TCGCCAGTGGAGGGA[C/T]GTAGGTTTTCAGCAC	4297
rs551378657	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118451530	GTAGCTGAGACTACA[A/G]GCACATGCCACCACA	4297
rs551471898	snp	A/G	0.000559938	0.0167229	missense	KMT2A	GRCh38.p7	11:118505796	ATGTATTTTGAACCG[A/G]CACCCCTGTTACCAC	4297
rs551473039	snp	A/G/T	1.65113e-05	0.00287322	intron-variant	KMT2A	GRCh38.p7	11:118499287	CTATTAACAGCTACC[A/G/T]TGGGTTTTATTTAAG	4297
rs551488819	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118455242	TCTGTCTCTCCATTA[A/G]ATTGTAGCTTCATGG	4297
rs551522109	snp	A/T	0.00279162	0.0372561	intron-variant	KMT2A	GRCh38.p7	11:118479313	TGTGGAGGTACTTTC[A/T]GCCATCTGGCATACT	4297
rs551535171	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118515067	CCACTGTGCCCGGCC[C/T]ATCCATGTGTCTTAA	4297
rs551537456	snp	C/T	1.67122e-05	0.00289064	missense	KMT2A	GRCh38.p7	11:118495875	ACTCCTCTGCATCCT[C/T]CTACACCACCAATTT	4297
rs551549047	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118469986	ACTTCATATAGGAAA[A/G]GAATTAGAGAGATCA	4297
rs551573591	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118450150	TTTCTGCTTTAGCAA[G/T]TAGATAAACCAGTTC	4297
rs551614247	snp	A/T	0.00318978	0.0398085	intron-variant	KMT2A	GRCh38.p7	11:118469174	CTTTATGGGACTCTT[A/T]TCTATCAGGCCACAT	4297
rs551635043	snp	C/G	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118467601	AACCTGCTAATTTGT[C/G]CTAAAAGTTATATAT	4297
rs551680091	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118487689	TTAAAAATCAAGGAC[A/G]TTCTCGTATTTAACC	4297
rs551742232	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118496670	TCCTCAAGAATATTT[C/T]GTGAAAGTTAATAAA	4297
rs551758865	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118488443	TACTCTGAATCTCCC[A/G]CAGTGTCCAATACTG	4297
rs551819015	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118486077	GACAGAGCAAGACTC[C/T]GTCTCAAAAAAAAAT	4297
rs551820238	snp	A/G	0	0	intron-variant	KMT2A	GRCh38.p7	11:118441973	TACCCTGTGGCTAGA[A/G]GGGGTGGCAACAGTG	4297
rs551826161	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118466748	TGAACCTGGGAGGCT[A/G]AGGTGGCGCCATTGT	4297
rs551922664	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118438215	GAAAGGACTTGGGGT[C/T]GTCTCTGATTCTTGT	4297
rs551965455	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118457433	CACCACGCCTGGCTA[A/G]TTTTTTTTTTGTATT	4297
rs552104331	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118446494	AGTGGCAGGGCTAGA[A/T]TTTAAATCTGAACCT	4297
rs552276253	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118494835	AGTTCTCATATTTCT[A/G]GATTGCAGTTTTCCA	4297
rs552302087	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118454574	CAACCATAGGCAATA[C/T]AGATGCTCCCCAACT	4297
rs552416138	snp	C/T			upstream-variant-2KB	KMT2A	GRCh38.p7	11:118434698	CACCCTTTTAGCATC[C/T]AGTAAACCACGCGCT	4297
rs552514608	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512810	TGTTTTTTGTTTTTT[G/T]TTTTTTATTTTAGAC	4297
rs552555743	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118465335	GTTCCCACGACCCCC[A/G]GTTCTTTAGGGATGG	4297
rs552581677	snp	G/T	1.64874e-05	0.00287113	missense, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512016	CGCCTAAAGCAGCTC[G/T]CATTTGCAGGTAATG	4297
rs552583822	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521601	CTGAGGATTAGTACA[C/G]AAAGTTGCTCTTAGA	4297
rs552631121	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118492294	CTAGAGGCAGGATTC[A/G]TAGTTAGGGGACAGT	4297
rs552668217	snp	A/G	1.90326e-05	0.00308479	intron-variant	KMT2A	GRCh38.p7	11:118482376	TCAGTCAGTACTAAA[A/G]TAGTCGTTGCCAGCA	4297
rs552680760	in-del	-/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521504	ACAAAAGAAATAGTG[-/T]TATGTTATCAATTCA	4297
rs552743834	snp	C/T	0.0023933	0.0345097	intron-variant	KMT2A	GRCh38.p7	11:118474899	GGAGGCCAAGGTGGG[C/T]GGATCACTTGAGGTC	4297
rs552787233	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118446273	AGAATCGCTTGAACC[C/T]GGGAGGCAGAGGTTG	4297
rs552789671	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118518626	TCTCTACTAAAAATA[A/C]AAAAAAATTAGCTGG	4297
rs552819570	snp	G/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118517310	CTGAGGCAGCAGAAT[G/T]GTGTGAACCCAGGAG	4297
rs552878891	snp	A/T	0.0023933	0.0345097	intron-variant	KMT2A	GRCh38.p7	11:118483187	GCAGTGAGCCGAGAT[A/T]GCATCATTGCACTCT	4297
rs552932611	snp	A/G	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118491674	TAGTAAGTTCAGTGG[A/G]ATAGTTTCCTCTTCT	4297
rs552970615	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118455758	GCTGGAGTTCAGTGG[C/T]GCAATCATGGCTCAC	4297
rs552976864	snp	A/C			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118516639	ACCTGTAAGTTCCTA[A/C]GGTCCTGTCTGGCAC	4297
rs552993181	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118481454	TTTTATGGCTGAATA[A/G]TACTCCATTGTGGAT	4297
rs553023123	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118479996	AAGGTAGGTGAAATT[A/G]CTGATCCAGGGATTC	4297
rs553029743	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118460288	ATATAGAAGGAAGAA[C/T]AGACTTTTTCTTTTT	4297
rs553095088	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118470482	TCTCGATATGCTTCA[A/T]TATTTGAGAAATGAG	4297
rs553110444	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118498256	GTTTTCAATTTATCA[A/G]TAGATAAAATGAATT	4297
rs553154860	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118443352	GAGCCGCTTTTCTTG[A/G]CCTATCCAAAGAAAT	4297
rs553171834	snp	C/T	0.00597247	0.0543191	intron-variant	KMT2A	GRCh38.p7	11:118507944	CTCCAGCCTGGGCGA[C/T]AGAGCAAGACTCCGT	4297
rs553213170	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118487385	GCCTGCACTGCACTC[C/G]TAAAGCATGACCAGT	4297
rs553218245	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118452198	AGTGCACACAACTAC[A/G]TCTGGCTCTGAATCA	4297
rs553222174	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118442523	GGAGTAAATCTCAGA[C/G]TCGTGATTTTTGTGG	4297
rs553286274	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118497604	AGTCTCCCTATGTTG[C/T]CCAGGCTGGTCTCAA	4297
rs553335144	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118459349	TGGGATTACAGGTGT[A/G]AGCCACCATGCCAGG	4297
rs553352573	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118496918	TGTAAAGCCTCTATT[G/T]GGTGCCTGGCACACA	4297
rs553370409	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118449777	CTCAGTCTTACTCCC[A/G]TTACTATTGGTCATT	4297
rs553394575	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118469614	TAATTCAGTTCTGTA[C/T]AGGAGAAAGCTATGT	4297
rs553425903	snp	A/G	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118448527	GAATTGGGATTATTC[A/G]TATAGATTACCAAAA	4297
rs553431704	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118457896	TCATTAATTTACTCA[A/T]CTGTTTTTAAGATTA	4297
rs553431895	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118443467	TGCTGCCAAACATTC[A/G]CTTCTAAAGACTTAA	4297
rs553489152	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118456720	TACTATATTCTTTCC[C/G]TGGGTGACTGAATTC	4297
rs553626055	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118467980	CCATCTTTCTTGAGA[A/C]CTTGTGCAAAATAGG	4297
rs553717686	in-del	-/AAAGA	0.00199481	0.0315187	intron-variant	KMT2A	GRCh38.p7	11:118446353	ACTGTGTCTCAAAAG[-/AAAGA]AAAGAAAAGAAAAGA	4297
rs553790474	snp	C/T	5.08712e-05	0.00504311	intron-variant	KMT2A	GRCh38.p7	11:118510128	TTGAAGGTGAGTGGA[C/T]TAAATCAGGTTGACC	4297
rs553808074	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118476151	CTCAGGTGATCTACC[C/T]GCCTCGGCCTCCCAA	4297
rs553913700	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118523676	ATTTAAAAGAAGATC[A/G]GTTTTTAATAATTTT	4297
rs553919297	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118457462	TTTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT	4297
rs553998740	snp	C/T	1.6473e-05	0.00286988	synonymous-codon	KMT2A	GRCh38.p7	11:118476882	AAGAGCAGCTGTTGC[C/T]CTTGGCCGAAAACGA	4297
rs554025495	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118437243	CCATCCCGGGACTGA[A/C]CCCCTCCTCCCTTTC	4297
rs554051422	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521202	CTCCTGGGGAACTAA[C/T]AGACCAGGAGAACTT	4297
rs554056481	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118502168	TAAGGCAGGAGAATC[A/G]CTGGAACCCAGGAGG	4297
rs554118330	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512429	TCAACAGAATACTTT[C/G]CAGGTTCTTCCCTTC	4297
rs554207321	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118485547	GGACTTTCTGTTGGT[A/G]GAAAGAAATATAGAT	4297
rs554229477	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118437717	TACAGTTTCTAGCCT[A/G]TTGGTAGCCGGGAAT	4297
rs554244083	snp	C/T	0.00203163	0.0318071	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118435125	TTCCAGCGAACTCCC[C/T]CTCGGCTTGGGGGAT	4297
rs554266191	snp	A/C	0.000296521	0.0121726	synonymous-codon	KMT2A	GRCh38.p7	11:118502915	ACAGGTTCATAACAC[A/C]ACATCTAGAGAACTG	4297
rs554273231	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118463628	TATTATGGTAGGAAA[A/G]CTATTCTACAGCCAG	4297
rs554334656	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118474619	AACTAAGGCTGAATG[A/G]ACTAAGGTTGGGACT	4297
rs554362741	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118447512	TTTTGTAAAGGTATT[A/G]ATTGGGGTTTTGAAA	4297
rs554407711	snp	C/G			upstream-variant-2KB	KMT2A	GRCh38.p7	11:118435606	GCCACCCAGCTTCAG[C/G]TTCGTTGTAACACCG	4297
rs554421662	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118481361	GTGATGTTTGTCTCT[C/T]TGTGTCTGGCTTATT	4297
rs554424269	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118447035	CTTTCCCATTTTGAC[C/G]TGTCTTGGGCTTATT	4297
rs554424447	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118455633	CTCCAATCCTTGCAT[C/G]TGATTTTCTTCCCCC	4297
rs554487393	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118454914	TGTGGCCCATAGTTT[C/T]CCAGTCTTCGGTAAA	4297
rs554559968	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118453092	ACCATATAAAACTAT[C/T]TGCCTTAATATAATC	4297
rs554592127	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118500298	TCTAAAACTATAAAT[A/C]CACACAATAATGATC	4297
rs554621034	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118444476	TAGTGGTGTGAGATC[A/G]TTTAGCATAGTAATT	4297
rs554686952	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118461573	GTGGCTATACTGTCT[C/T]GGAATGCTGTGCTCA	4297
rs554732759	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118468133	TTTCATCCTATATGC[A/C]GTCAATTCATGATCC	4297
rs554753181	in-del	-/AA			upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118525658	CACAAAAATAAAAAA[-/AA]TATTCTAATGAATGT	4297
rs554777115	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118435659	GGCCTCAGTGCCCGG[C/G]CTGGAGAAACACAAC	4297
rs554810090	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118500795	ATTTTCTGAGAGGCT[A/G]AGAAAAACCAAGGAC	4297
rs554838866	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118445348	GTGCCTCCATGAGTT[A/G]CTAATTATCAGGCCA	4297
rs554929369	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118460469	TTTTTTGTATTTTTA[A/G]TGGAGATGGGGGTCT	4297
rs555023370	snp	C/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512644	TATTTTTTTTCAGTA[C/T]ATACCTCAGAGTGGA	4297
rs555046348	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118519267	GCCTGTTTGCTCACC[C/T]GAAAATGAAGCTAGT	4297
rs555054058	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118518830	CACCTGTAATCCCAG[C/T]ATTTTGGAAGGCCAA	4297
rs555088832	snp	A/C/T	3.29648e-05	0.00405974	missense, intron-variant	KMT2A	GRCh38.p7	11:118472843	ACCTCCTCGTCTCCA[A/C/T]CTCCACCTCTGCTGA	4297
rs555154152	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118442464	TATTTCCTTGGATCT[C/T]ATCTAGACTGGTTTA	4297
rs555188885	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118507851	GCCTGTAGTCCCAGC[C/T]ACTCAGGAGGCTGAG	4297
rs555217482	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118451685	TTTTGTAGAGATGGG[C/G]TCTCACCATCTTATG	4297
rs555249560	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118525431	CCACCCACCACCTCT[C/T]GCACAGCCCCTCTGT	4297
rs555259966	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118517268	AGGCGTGGTGGCGGG[C/T]GCCTGTAGTCCCAGC	4297
rs555277053	snp	A/G	6.60567e-05	0.00574665	intron-variant	KMT2A	GRCh38.p7	11:118480290	TTGCTTAAATGGTGT[A/G]TAGTTGTATACACCC	4297
rs555310772	snp	C/T	0.00234209	0.0341403	missense	KMT2A	GRCh38.p7	11:118506582	AAAGTTTCCCATTTG[C/T]GGACCAGTTCTTCTG	4297
rs555399991	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118489029	AGTTCGAGACCAGCC[G/T]GAGCCAACATGGTGA	4297
rs555409991	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118494960	TGTTCTTTACTTTTA[C/T]ATTTGTTTTATTGTA	4297
rs555459464	snp	C/T	9.88354e-05	0.00702908	synonymous-codon	KMT2A	GRCh38.p7	11:118498025	GTTTGAAGATGATGA[C/T]GGATCACTAAAGAAT	4297
rs555485233	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118441902	CATCTCTTTGCTCAC[C/T]TTAGAGCTGTCCTTC	4297
rs555520003	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118507158	TTTAAAACAGCTGGG[C/T]GTGGTGTTGCACACC	4297
rs555554390	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118450671	TTCTCAATATCAGGC[A/G]GAGATCATATTTAAA	4297
rs555608383	snp	A/C	0.0023933	0.0345097	intron-variant	KMT2A	GRCh38.p7	11:118460071	AAAACATTACAGTTT[A/C]TCAGTTGAAATTTTA	4297
rs555677951	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118497092	TCACTACAACCTCCG[C/T]CTCCTATGTTCAAGC	4297
rs555679853	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118459067	GGATTTGATTTTTCA[A/G]ACTCTTTTTTTTCCC	4297
rs555706943	snp	C/T	0.0023933	0.0345097	intron-variant	KMT2A	GRCh38.p7	11:118440440	CTGTACTTTGCCATC[C/T]AAATAAACATAGTAC	4297
rs555750078	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118456636	AGCCGCCGCGCCTGG[C/T]ATGCCTATATATTTC	4297
rs555750258	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118442706	AGTTAATTAAGAATA[C/T]CCTTGTAGGCTCCAC	4297
rs555768018	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118449458	GCATGGTGGCCTGGC[A/G]CCTTGTAGTCCCAGC	4297
rs555806941	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118515135	TGGAGCTGAGAAAGC[C/T]GAATTTTTAACATGT	4297
rs555809633	snp	A/C	0.00199481	0.0315187	intron-variant	KMT2A	GRCh38.p7	11:118466812	TCAAAAAAAACAAAA[A/C]AAAACAAAACAAAAA	4297
rs555872890	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118465992	ATTTATTTGGGGTTC[A/T]GATTCACATGTTGTA	4297
rs555889168	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118489308	CACCATTTTGTCTAG[A/G]GACTTGGGCATCCAT	4297
rs555893489	snp	A/G			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118523649	TATTTTTTAAACCGC[A/G]GTATTATCCTAATTT	4297
rs555997103	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118442581	TCAGATGAAATTATT[C/G]ATTGCTCCTAAGTTG	4297
rs555998401	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522302	CTCTGTGATGGCTGA[A/G]CTCTCTTATGTCCTA	4297
rs556011318	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118438876	AGCTAGCTGCAGCGT[C/T]CCCTTTCCCTGCCTC	4297
rs556071121	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118448457	CTCAGAATGAAACCT[G/T]TTTAGATATGTTGGG	4297
rs556107767	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118514354	TCATCTGTTCAGTCT[C/T]AGCTTTCCCCACTTC	4297
rs556162756	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118437120	GCAGACCCCCAGGCG[C/G]CCCCACCCCGGGGTT	4297
rs556215502	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118484654	GTATTTTCGCAATAT[A/G]TTCAATATGAATTGA	4297
rs556259724	in-del	-/AAAT	0.00716266	0.059414	intron-variant	KMT2A	GRCh38.p7	11:118475134	TAAGTCTCTATCTCA[-/AAAT]AAATAAATAAATAAA	4297
rs556318781	snp	C/T	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118476062	GGGCATGCACCACCA[C/T]GCCCAGCTAATTTTG	4297
rs556360921	snp	A/T			synonymous-codon	KMT2A	GRCh38.p7	11:118495796	CCACACTGAGCAGCC[A/T]CCTTTAATGAAGAAA	4297
rs556380142	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118485447	GTGGCAGGGGGAGGT[A/G]AAGGGAGGGTGTCTG	4297
rs556463636	snp	A/G	0.00199481	0.0315187	intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118511501	TTAGAGCTGGAAGGA[A/G]CTGTAAGGATTTTCT	4297
rs556527243	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520440	GACAGATCATGAGGT[A/C]AGGAGTTCGAGACCA	4297
rs556592051	snp	A/G	0.000399281	0.0141238	synonymous-codon	KMT2A	GRCh38.p7	11:118493185	GCAGCCTTTAGATCT[A/G]GAAGGAGTCAAGAGG	4297
rs556602909	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118446718	ATCTTCTCATTGGTC[G/T]TCCCACCTATCTTTT	4297
rs556639970	snp	C/T	0.00159617	0.0282053	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512294	CTATTCATTAGCAGT[C/T]ATTCCTCAGCCCCTG	4297
rs556652833	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118501971	GAAAATGTAGATTCC[A/G]GGTGGGTGAGGTGGC	4297
rs556703175	snp	A/C	0.00438332	0.0466095	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521138	TTGGCCATGTGTTAG[A/C]TGGCCAAATCAAGTG	4297
rs556778557	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118499218	TTGAGATATGCTATG[G/T]GCCTTCCACTCTGAG	4297
rs556841574	snp	G/T	0.00358779	0.0422022	intron-variant	KMT2A	GRCh38.p7	11:118509045	TTTCTAGCAGTTATT[G/T]TGTATACCACAGCTG	4297
rs556857791	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118484479	GAGCTTTGGTCAGTG[C/T]TGTTAGGTCACTGTT	4297
rs556867251	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118463345	TGCTTGAGCTGTCAA[C/T]CATTGTAGCATTTGG	4297
rs556907816	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118483482	AGCCTGCAGTGAGCC[A/G]AGATCGCGCCACTGC	4297
rs556928410	snp	A/G	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118462753	TTTTTTAGTAGAGAC[A/G]GGGTTTCACCGTGTT	4297
rs556928784	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118474513	GACATAACATTCTAA[A/G]TAGAGGGAACAGTGT	4297
rs556971085	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118492408	CACGGGGCCGGGCGC[A/G]GTGGCTCACGCCTGT	4297
rs557019904	snp	A/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118514437	CCAGATCCATCCATG[A/T]GTCTTTTTTTTTTTT	4297
rs557021774	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118500619	GGTTTGCCCTTTGTT[A/T]TATTTTCAGGCCGTA	4297
rs557066711	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118470554	TAATTAGGATATGTT[A/G]AGAAAGGAGCTGTGA	4297
rs557076786	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118507900	CCCAGGAGGCGGAGC[C/T]TGCAGTGAGCTGAGA	4297
rs557084225	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118460958	TTGTATCTGGAACAT[A/G]TAGCCCTAGGGCAAG	4297
rs557098835	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118490348	AAAAAGTCTCACACA[C/T]TATGTCAAGGATACC	4297
rs557143783	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118444366	AAGCTTAGCTAATGA[A/G]GAAATCCTTTTGTAA	4297
rs557209079	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118452883	GTGATCTGCCCACCT[C/T]GGCCTCCCAAAGTGC	4297
rs557325720	snp	C/T	0.0023933	0.0345097	intron-variant	KMT2A	GRCh38.p7	11:118488840	TCAACCAACCTTGGA[C/T]TGAATGTATCTGGGA	4297
rs557352644	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118441770	CATGTCCCCATCTTT[A/C]ACTTCCATTTAATTA	4297
rs557397215	snp	A/G	0.00358779	0.0422022	intron-variant	KMT2A	GRCh38.p7	11:118460413	CTACCTCAGCCTCCC[A/G]AGTAGCTGGACCACA	4297
rs557438229	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118526758	AAAGGAGTTTTTAAA[C/T]ATGTTTATTTTCTAT	4297
rs557478747	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118456874	TCCTTTAAACCTGTC[G/T]CCTTTCTGTGTTCCC	4297
rs557504584	snp	C/T	0.0023933	0.0345097	intron-variant	KMT2A	GRCh38.p7	11:118461563	TTTAGGTTTTGTGGC[C/T]ATACTGTCTTGGAAT	4297
rs557652052	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118487937	TATAATCCCAGCACT[C/T]TGGGAGGCCGAGGCA	4297
rs557830458	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118507083	AGAAGGATTGCTGGA[A/G]CTCAGGAGTTCAAGA	4297
rs557841427	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118500067	CTCGGATTCGTCTGC[G/T]TGTAGATTGGGACTA	4297
rs557856601	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118487118	TGCAGAAGTTCAGAT[A/G]TCATTGAGACTGAGA	4297
rs557882878	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118449858	AATAAGAACAACAAA[C/T]GGAAGAAAAAAACTG	4297
rs557891829	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118516271	GACAGGAAATCTGGA[A/T]TCTCTTGATGAGGCA	4297
rs557924781	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118449423	TAAATTTAAAAAATT[-/A]AAAAAAAAAAATTAG	4297
rs557944528	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118457959	CTCTGTTTTCATACC[A/G]TAGCCTAGGAATGGC	4297
rs557951262	snp	A/G	0.00159617	0.0282053	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118515553	ATCTTCAAGCTGATA[A/G]CAAATGGCTGCAGCA	4297
rs557958957	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118523934	CAAAAGGCTACAGTA[A/G]TATCTTGATACAACA	4297
rs557966718	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118514187	ATCTTCAACCCTTAC[A/G]TATTTGTTATTAGTA	4297
rs557972584	snp	A/G	1.64942e-05	0.00287173	synonymous-codon	KMT2A	GRCh38.p7	11:118503062	CACAGATTCTACCCA[A/G]TCAGCAAACTCCTCT	4297
rs558048708	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118494526	TTTGGTTTAATTTGA[C/T]CCCCTGATTCTTTGA	4297
rs558066156	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118491017	TTTCTGTGAGTATTC[A/G]AGGGGCTCAGAATAA	4297
rs558119471	snp	A/G	0.00358779	0.0422022	intron-variant	KMT2A	GRCh38.p7	11:118467143	GCACTTTGGGAGGCC[A/G]AGGTGGGCAGATCAC	4297
rs558184405	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118486591	GGTAAAGAAAATCCA[C/T]GTCGGGTGCAGTGGC	4297
rs558277695	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118454977	CTAGCGAATATAACC[C/T]CACAGCTAACACCTC	4297
rs558319950	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118484554	TCCTGAGCAGTATCA[A/G]AGGAAGTAATTCCTT	4297
rs558382037	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118483656	TAAAGGCCATTTGGC[C/G]TAATTATTTTTTGAC	4297
rs558405021	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118437785	TGAAGGATTAGTGGC[A/T]TCTTGGAGGGGAAAA	4297
rs558413828	snp	A/G/T			intron-variant	KMT2A	GRCh38.p7	11:118482201	GATTTGAAGTCTTCA[A/G/T]TTCAAGAAAATCAGC	4297
rs558474126	snp	A/C/G	0.000690846	0.0185727	intron-variant	KMT2A	GRCh38.p7	11:118447579	TTTATGTAGATAATA[A/C/G]TTAGCACTGATCATC	4297
rs558477219	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118435881	CTTCTGTTTTGCATG[C/T]AGTACAATAAGGGCT	4297
rs558532733	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118485606	TATTTGGAAATATAT[A/G]TCTATCTTTAAAATA	4297
rs558593023	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118492540	AAAAATTAGCCAGGC[A/G]TGGTAGCGGTCACCT	4297
rs558656161	snp	C/G	1.6698e-05	0.00288941	intron-variant	KMT2A	GRCh38.p7	11:118500947	AGTTTCTGCTTCTAT[C/G]CTCTCCCTTATGATG	4297
rs558767603	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118492882	CTAGCTAAGCTATTA[C/T]ATAACAGTCTCATTT	4297
rs558823598	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118453131	AAACGCTTGACCCCA[C/T]GTCCACCTCTAGCTG	4297
rs558886656	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118462680	TCTCCTGCCTCAGCC[C/T]CCTGAGTAGCTGGGA	4297
rs558969875	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118475441	TGTAATGTTATTCAC[A/G]GGCTGGGTACGGTGG	4297
rs558987090	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118453787	AGTATCACTAGTATT[C/T]CCATTTCATAGGCAA	4297
rs558987194	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118475115	TCCAGCCTGGGCCAA[C/T]AGAGTAAGTCTCTAT	4297
rs559013973	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118483383	TAAAAATACAAAAAA[-/A]TTAGCCCGGCGAGGT	4297
rs559036994	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118527152	AGTATTGATTTTTAT[C/T]GGTTTTCTCAACTGT	4297
rs559047647	snp	A/G	0.00914312	0.0669923	intron-variant	KMT2A	GRCh38.p7	11:118463188	GTCTTGCACTCCTGG[A/G]GTCAAGCAATCCTCC	4297
rs559099337	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520188	AAAAGGACTGAAAAC[C/T]ATTTGTGTTGAAGTA	4297
rs559106168	snp	A/G			missense	KMT2A	GRCh38.p7	11:118503906	CAGGTGGATGGGGCC[A/G]ATGACTTAAGCACTT	4297
rs559186919	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118509707	ATCAGATCGTCATAC[C/T]AGAAATTCTACCACA	4297
rs559239789	snp	C/T	1.86468e-05	0.00305337	intron-variant	KMT2A	GRCh38.p7	11:118471635	CAGCTAAATATATGC[C/T]CTTCATTGTTTAATT	4297
rs559290078	snp	A/T	0.000798403	0.0199641	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118516463	CAGTGAAACTCTCTT[A/T]AAAAAAATTAAATTA	4297
rs559359542	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118469959	CTCTTTAACATGTGA[C/T]GAAGTCTTAAAACTT	4297
rs559388214	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118507279	TCCAGCCTAGGTGGA[A/G]TGCACCTATGTAGCC	4297
rs559393545	snp	C/G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118443929	TTGGGTATAGATGTT[C/G/T]TGATGTCTTTCAGCA	4297
rs559414688	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118524243	AAGCAGATTTTTCTC[C/T]GCCTCTGCCACAAGG	4297
rs559420164	snp	C/T			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118524513	CTGTGGCCAGGATGG[C/T]AGAGACTTCCTTGTC	4297
rs559424041	snp	A/G	0.0023933	0.0345097	intron-variant	KMT2A	GRCh38.p7	11:118476746	GTATACCTTGGCTTC[A/G]TTCAGTTATAATTTC	4297
rs559442160	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118480594	TGTTGTGTCACATTT[A/C]TACGCTTCTATTTTT	4297
rs559471742	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118523294	TTTTTAAACGGTCAG[C/T]GTCCAGTTGAAGGCA	4297
rs559565422	snp	A/C/G	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118488382	GTTAAATCTTGTATT[A/C/G]TATTTATTTTGTTAC	4297
rs559580450	snp	A/G	0.00199481	0.0315187	intron-variant	KMT2A	GRCh38.p7	11:118477393	CAGAACAAATTTAGA[A/G]GTTTGAAGAATCCTT	4297
rs559583811	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118495196	ACGGAGTCTCGTTCT[A/G]TCACCAGGCTGGAGT	4297
rs559631998	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118464363	CAACATGACGAAACC[C/T]CATCTCCACTAAAAA	4297
rs559632544	snp	A/G	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118486759	GTGCCTGTAGTCCCA[A/G]CTACTCTAGTCCCAG	4297
rs559663507	snp	A/G	0.000214142	0.0103453	missense	KMT2A	GRCh38.p7	11:118506366	ACCCAGACGGTAGAC[A/G]CTCCTAATAGCATGG	4297
rs559726304	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118441204	AGTCAGGGTCTCACT[A/G]TGTTGCCCAGGTGCA	4297
rs559853821	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118447930	AAAAAGGTTACCAAA[A/G]TAATTTTATTATCTT	4297
rs559896131	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118467450	CCTTTTCTTAAATAG[A/T]CCAATACTTTAATCT	4297
rs559916897	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118455902	ACATTGTTGCCCAGG[C/T]TGGTCTTGAACTGCT	4297
rs559918363	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118492407	ACACGGGGCCGGGCG[C/T]GGTGGCTCACGCCTG	4297
rs559933522	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118437967	GCTGCTCTCCTACCC[C/T]ACCCACTGCGCCTGA	4297
rs560038892	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118499243	TCTGAGACAGTCAGG[A/T]TCATAAGTATAATGT	4297
rs560045207	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118486577	ATGTATTCAAAGGTG[G/T]TAAAGAAAATCCACG	4297
rs560096677	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118445322	AGGCAAGTAAGATAC[C/T]GAGGAACACAGTGCC	4297
rs560114932	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512805	TTACCTGTTTTTTGT[G/T]TTTTTTTTTTTATTT	4297
rs560132433	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118494798	ATAACTTTTTTTTCT[C/G]CTCATCGGCTAGAAA	4297
rs560158256	snp	A/G			upstream-variant-2KB	KMT2A	GRCh38.p7	11:118435785	GAGCTCCAGCATGAA[A/G]ATGGGAGGGGCTCCT	4297
rs560173852	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118438138	ACAGTTATACTTTAG[C/T]GTGGTGGCGGTGGTT	4297
rs560252699	snp	A/T	4.95045e-05	0.00497492	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521446	TTGCACTCACACAGT[A/T]CTTTTGTTTTGCTGT	4297
rs560329727	snp	C/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118513851	CTGATGTGGGAGGAG[C/T]GCATTGAGCCTGGGA	4297
rs560334184	snp	A/C	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118474845	AATGAGAAGTACTGG[A/C]CAGGTGCGATGGCTC	4297
rs560353951	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118513505	TTGTTCATTTTATGT[A/G]ACAGGTACATGCATG	4297
rs560417477	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522340	ATCAGACATGTGATC[A/G]TAGTCCCAGAGACAG	4297
rs560463865	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521532	TCAGAGACCTTTCTT[A/C]AAAAAATAAACTCTG	4297
rs560527889	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118475540	CATCCTGGCTAACAC[A/G]GTGAAACCCTGTCTC	4297
rs560562240	snp	A/G			utr-variant-3-prime, intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118525110	AAAGAAGGCAAAAAC[A/G]GCACAGCTATCTCCA	4297
rs560592573	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118483803	TTGGGGGGCCAAGGC[A/G]GGAGGATCACTTGAG	4297
rs560592574	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118493364	TCACGTGGCTTTAGA[C/T]ACCTAAAAATGTATG	4297
rs560603386	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118435395	CAGAGCTCGCCGCCG[A/G]CGGGCCCCTTCCACC	4297
rs560660299	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118444986	ATGCATGTAAGCACT[C/T]AGCATTTTGCCTGGC	4297
rs560785779	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118501209	ACGCCTGTAATCGCA[A/G]CACTTTGGGAGGCTG	4297
rs560810459	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118453977	AGATTTATCGTCGAT[G/T]TATCTCTTTTATTCA	4297
rs560820420	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118445867	AATTAGCTGGGTGTG[G/T]TGGTTGCGCACCTGT	4297
rs560871800	snp	A/T	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118490466	TCATTATAACTAACC[A/T]CAAAGAAATCCTCTA	4297
rs560915401	snp	A/G	0.000399281	0.0141238	missense, intron-variant	KMT2A	GRCh38.p7	11:118472609	TCTAGTAGCCCCAGT[A/G]TTGATACCTCCACAG	4297
rs560933520	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118489599	TAATATGAATACTCA[C/T]CACTGAGTGCCTTTG	4297
rs560958795	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118465422	AGAAATAAAATTTAT[A/C]TTTTTAATTTTTATC	4297
rs560993536	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118462072	AATTCTCGTGCCTCA[A/G]CCTCCCGAGTAGCTG	4297
rs561065915	snp	A/G	5.00914e-05	0.00500432	missense, intron-variant	KMT2A	GRCh38.p7	11:118473738	CCGAGGAGCTGTCCA[A/G]AGATCGAGATGCTGA	4297
rs561096499	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118454164	TGTTTCTCACATAGC[A/G]ACAGTAAACTCTGGT	4297
rs561159545	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118457735	CTCCCCCACCCCCCA[A/C]CAGCTTTATCATCCT	4297
rs561191141	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118445982	ACACTCCAGCCTGGG[C/T]GAAAGAGCAAGACTC	4297
rs561202068	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118442778	ATTTTCAGAATAAGA[C/T]AAAATAGCTTTTCTG	4297
rs561236770	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118508223	TAACGTGGTATATAT[A/G]TGAATATGTATACAC	4297
rs561253995	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118515078	GGCCCATCCATGTGT[C/T]TTAAAGTGTAGCCTA	4297
rs561284345	in-del	-/A	0.00755907	0.0610114	intron-variant	KMT2A	GRCh38.p7	11:118485368	AGGAATGACATCCAG[-/A]AAAAAAAAATAGGCA	4297
rs561296039	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118518044	CAAACTGTATGTCTG[C/T]TGGAATTGCATATGT	4297
rs561350981	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118443662	AAAGATATAAGAGTT[A/G]GTTGGCAGTTTTGTG	4297
rs561452141	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118469897	TAGTTGGGGGCAGTT[A/G]GCCAGTAGTGTCCCA	4297
rs561493578	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118440819	GTTTACTGGTCATGT[A/G]TGTACCAAGAGTGGG	4297
rs561500118	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB, downstream-variant-500B, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118527038	TCAGTGATGTATGTT[C/G]AGGACCTAATTAATT	4297
rs561518797	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118479238	AGCCATCCCCTAATA[G/T]GGAATTTTTTATGTG	4297
rs561563033	snp	A/G	0.00438332	0.0466095	upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118526148	CCCGAAATGGGGGGA[A/G]CCTCTAACCATAAAG	4297
rs561680189	in-del	-/A	0.00199481	0.0315187	intron-variant	KMT2A	GRCh38.p7	11:118495167	TTTATTTATTTATTT[-/A]TTTTTTTTTTGAGAC	4297
rs561716503	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118524135	TCCCTCTGCCCACCA[A/G]GTCCTCATATCTGCA	4297
rs561725360	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118488242	AATGGAAAGGACAAA[C/T]CAGACCTTACAACTG	4297
rs561748420	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118440966	GCTCTCATCTCCGTT[A/G]CTGAACAGTTATGAG	4297
rs561786764	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118497298	GTGAGCCACCGTGCC[C/T]GGCCAAAAGCTTTTA	4297
rs561813587	snp	A/C	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118449953	CTTGTCATATGGGGG[A/C]CCAAAATTTCTTATA	4297
rs561846584	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118515713	TTTTTTTGAGACAGG[G/T]TCTCACACTGTTGCC	4297
rs561851428	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118496403	GGCCCTAGTTAATAC[A/G]TACTCCAAAAGAACT	4297
rs562004782	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118458060	TCCCTATGCATTTTT[C/T]TTTGAGATGCTTTCA	4297
rs562013159	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118441250	CCTCCTGCCTTAGCC[C/T]CCTGAGTAGCTGGGA	4297
rs562013258	in-del	-/A	0.00318978	0.0398085	intron-variant	KMT2A	GRCh38.p7	11:118492029	ACTTAATTTTTAGTT[-/A]ACTTGTTTTGGCTAT	4297
rs562017467	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118465001	ATGTCCCTGCTCATT[C/T]CTCTCATCAAACAAG	4297
rs562027971	snp	A/G/T	1.64781e-05	0.00287033	missense	KMT2A	GRCh38.p7	11:118505434	TCCCACCAAACATCA[A/G/T]CAATCCTCCTTCAGG	4297
rs562056538	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118448917	GAACAAATTCATACT[C/T]TCCCTATAACTTTTA	4297
rs562066180	snp	C/T	0.00199481	0.0315187	intron-variant	KMT2A	GRCh38.p7	11:118494604	GCCTGAAATTATCCT[C/T]GTATTAACAGAGAAG	4297
rs562071227	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118477144	TAGAAGAAATGCCTG[A/G]GAAGGAAAACGGGGA	4297
rs562080859	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118444607	TTGAGACAGGATCTT[A/G]CTTTGTTGCCTAGGC	4297
rs562088498	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118514703	CAATGGCGCAATCTC[A/G]GTTCACCGCAACCTC	4297
rs562132138	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118467400	AAAAAAAATTATAAT[A/G]CTTTTTCAGATGTCT	4297
rs562189014	snp	C/T	1.75259e-05	0.00296017	missense	KMT2A	GRCh38.p7	11:118502409	TTAGGAAGTCCTACC[C/T]CAACCACTCATGAAA	4297
rs562193280	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118466324	GACAGAGTGAGCACT[A/G]GCAAATTTTAAAATT	4297
rs562275944	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118455158	AGCCTTCCTGGTAGC[C/T]AGGATTACAGGCGAG	4297
rs562292744	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118437840	AGAAGAGCAGCTTTC[C/T]ACCACTCCCCTTGGA	4297
rs562295657	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118478497	ATGTGGCTATTGAGC[A/G]CTTGACATGTGATTA	4297
rs562338891	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118464980	GAGTCCTGCTCCATC[A/C]TGGCAATGTCCCTGC	4297
rs562352863	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118447782	AACATGAATGGATCC[A/G]TTATTAGGAATGGTA	4297
rs562357550	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118482999	GCACTTTGGGAAGCC[A/G]AAGCAGGCAGATCAC	4297
rs562389969	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118513318	TGACTTTGTTTTATC[C/T]ATATCTACCTCTCCT	4297
rs562411051	snp	G/T	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118464006	GAATGGTGAAATCAT[G/T]GATGCTTTACATAAA	4297
rs562433761	snp	A/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520504	AAAAATACAAAAATT[A/T]GCCCGGCGTGGTGGC	4297
rs562474306	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118474745	TTTTACTATCCCCGA[C/T]AGAATAGAAAACCGG	4297
rs562477650	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118437538	TCCTTCACCTCCACC[C/T]TCTACCCCCACCCCA	4297
rs562484392	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118446190	CCTGTCTCTACTTAA[A/T]ATACAATAATTAGCT	4297
rs562518283	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118511882	AGCAGTGCTTGTGCA[C/T]ATCATTGGTATTAAG	4297
rs562547345	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118454399	GTTGCTGTCTTGGGG[A/C]CTTTGCACTTGCTCT	4297
rs562573543	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520713	GCATTAAACAAAGAG[G/T]GTACTAATTGTCTCT	4297
rs562576040	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118447107	TCTTCCATGAAGTTT[C/T]CACAGATTGTACTGC	4297
rs562597737	snp	A/C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118475452	TCACGGGCTGGGTAC[A/C/G]GTGGCTTACGCCTGT	4297
rs562629128	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118436118	TCCATCCTCCGCGTA[C/G]TCCTCGCCCCCTCCC	4297
rs562691965	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118435266	GCGTCTAACGCTATG[C/G]TCGAGGCGCCCTCCC	4297
rs562753908	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118434625	AACCGTCCACAATGG[A/G]GTGTCTCTGTCCTTA	4297
rs562799896	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118482998	AGCACTTTGGGAAGC[C/T]GAAGCAGGCAGATCA	4297
rs562861276	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118492134	AAAGGTCTTGCTGTT[A/T]CAATGAGAAATTTGG	4297
rs562928572	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118492583	ACTCGGCAGGCTGAG[A/G]CAGGAGAATGGCGTG	4297
rs563073039	snp	G/T	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118452695	CTGGAGTGCAGTGGC[G/T]CCATCTCGGCTCACA	4297
rs563121921	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118510482	GCCTGGAGTTCTCTC[C/T]CTGCCCTCAATCACC	4297
rs563165614	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118453242	TTCATTCTTTCCTCA[A/G]CTACTCCAGTTGGGC	4297
rs563183217	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118509448	CCATACTCTTCTGCT[A/G]TACTGGTTTTACCAG	4297
rs563208077	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519453	GATAGATCTGTATCA[A/G]CATCATTTTAATGGC	4297
rs563211966	in-del	-/G			intron-variant	KMT2A	GRCh38.p7	11:118474996	AAATTAGCTGGGCGT[-/G]GTGATGCATGCCTCT	4297
rs563235715	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118510581	GCCCTCCCTCTCCCT[C/T]CTTTTGAATCTTACA	4297
rs563235802	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118459633	TAAAGAACTCTAGGC[A/G]GGTGATTTTTGCTCT	4297
rs563247438	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118498302	TGGGATGAGTCTATA[C/G]AGGAGACGGTAAACG	4297
rs563296550	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118465125	ATCTATGAAGGAGGC[A/G]GAGCATCTAGGCTGA	4297
rs563325896	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118497641	GGGCTCAAGCGATCC[C/T]ACCACTTCAGCCTCC	4297
rs563331233	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118461125	TATGTTTAATACTTA[C/T]TTAGGGTTCACTTAG	4297
rs563370323	snp	A/G	0.00199481	0.0315187	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521538	ACCTTTCTTAAAAAA[A/G]TAAACTCTGAAATTT	4297
rs563379183	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118489325	ACTTGGGCATCCATG[A/G]ACTTTGGTATCCTCT	4297
rs563389604	snp	A/G	0.00199481	0.0315187	intron-variant	KMT2A	GRCh38.p7	11:118507444	TATCAGATCCTGATA[A/G]AGCCATTTCTTTCGA	4297
rs563390985	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118471032	GTGGACACATTATGT[C/T]ACTTCACTGATTAGT	4297
rs563497795	in-del	-/TA	0.00755907	0.0610114	intron-variant	KMT2A	GRCh38.p7	11:118469331	TGTTATGTGGTAGTG[-/TA]TATATGTCTTTGGGA	4297
rs563537718	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118469711	TTTTATGTGGATAGA[C/T]ACTCCAGCTAAATAT	4297
rs563599025	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118468729	TGGGATGTGTTTGTA[C/T]GCACGTTTTTGCTTC	4297
rs563600676	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118451162	CAGCTACTGGGGCTC[C/T]ACCATTGGAGACGTC	4297
rs563663655	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118459504	TAGAAAAGGAAGGTG[A/G]GGGTGTGAGCAAAGT	4297
rs563702560	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118526005	TATATAGGAACTAAT[A/G]TAGTAATGCACCATG	4297
rs563724002	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118478543	CACACTGTTTATTTC[C/G]TTTAACTTTAGCCAT	4297
rs563837431	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118450189	AACCTGAGGATTCTG[A/G]AAATACACCTTTCTT	4297
rs563900307	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118458458	ATTTTCTACTATAGT[A/G]CTATTACCACAGTAG	4297
rs563942926	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118524472	AACATTGTCACTGTT[C/T]TCACTGTCATGCAGG	4297
rs563976087	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118438100	GGGGGAAGCCAGGTT[A/G]GGGTGAGGAGAGTAG	4297
rs564138763	snp	C/T	0.00279162	0.0372561	intron-variant	KMT2A	GRCh38.p7	11:118448834	CAATTGTTGGCAAAG[C/T]GAAGGGCAGTTTGAC	4297
rs564150671	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118486898	GTCTCAAAAAAATTT[A/T]TAAAAATTTAAAAAA	4297
rs564199515	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118457084	CTGTTCTTCCTGCCT[C/T]TACTTCTCTACTGCT	4297
rs564213616	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118495500	TTGTTTCAGCAAGTT[C/T]AACCAAGAGTCATAT	4297
rs564267796	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118443531	GTAATTGTTGTGGAT[G/T]ATATAAATCCCCTTG	4297
rs564302711	snp	A/T	0.000798403	0.0199641	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118514632	TATTATTATTTTTTT[A/T]TTTTTATTTTTATTT	4297
rs564364113	snp	A/G	0.00119737	0.0244387	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118513850	GCTGATGTGGGAGGA[A/G]CGCATTGAGCCTGGG	4297
rs564379757	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118448006	AAAATGACCTCTTAA[A/G]CTACCTTTTCCTTCT	4297
rs564383105	snp	C/G	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118465345	CCCCCAGTTCTTTAG[C/G]GATGGGCTAAATAGC	4297
rs564391923	snp	A/G	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118440912	AACACAAGCAGAGTG[A/G]AGTGCACGAAGCCTC	4297
rs564439338	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118485624	TATCTTTAAAATAGG[C/T]ATATCCTCTAACATA	4297
rs564442168	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118456115	TGCTAGGATTATAGA[C/T]GTGAGCCACTGCACC	4297
rs564458541	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522491	AGGGTTGGTTATGTT[A/G]GGAGATTGGGCCTGA	4297
rs564507404	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512535	TGTTGCTTATCCATT[C/T]ATTAGTCAGTGGACA	4297
rs564529574	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118486842	GCAGTGAGCCATTAT[C/T]ACGCCACTGCACTCC	4297
rs564634683	snp	A/T	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118483185	CTGCAGTGAGCCGAG[A/T]TTGCATCATTGCACT	4297
rs564681854	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118484782	GTGATGTCACACTAA[G/T]TTTATGCTTTTCATC	4297
rs564690648	snp	A/G	0.0001812	0.00951667	missense, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519741	AGCCAGAGGAGGCCA[A/G]TGAACCCCCCTTGAA	4297
rs564693995	snp	C/G	0.0023933	0.0345097	intron-variant	KMT2A	GRCh38.p7	11:118501376	CAGGAGGCAGAGGCA[C/G]AAGAATCACTTGAAC	4297
rs564752704	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118437449	GTGTCCCTTCCAGCA[A/C]CTTGCTTTCGAAAAC	4297
rs564815953	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118436373	GGCCCGGCGCTCTGC[A/T]TAGCGGCCGGCAGGG	4297
rs564817477	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118447062	TATTATTCGTCTCCC[A/G]TGGTTCAACTCAGAT	4297
rs564851534	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118482638	CTTTTAGCTGGGCAC[A/G]GTGGCTCACGCTGGT	4297
rs565026072	snp	C/T	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118463821	TCAAAATTTTGTATG[C/T]ACCAAAATAAACTTG	4297
rs565084981	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118443830	ATCGGTCCAGTAGCA[C/T]TTATTTCAGGAGCTG	4297
rs565128826	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118462245	AGGTGTGAACCACCA[C/T]GCCCGGCTGCAGCAC	4297
rs565148361	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118452609	CCTTCTACCATCAAA[A/G]AAGTGCCCCCTTCTT	4297
rs565447335	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118509262	AAGGATTATGAGAAT[C/T]ACCCACTTTACCTAC	4297
rs565477048	snp	A/G	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118460702	TGGCTATGTTGCTCA[A/G]GCTGGAGTGCAGTGG	4297
rs565503838	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118518857	CCAAGGCGGGTGGAT[C/T]ACGAGGTCAGGAGAT	4297
rs565547145	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118461839	CCAACACTCTTACCT[G/T]GTTTCCAACCTCCAG	4297
rs565566583	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118518122	CCAAAATTAACACCA[C/T]TACTGTTTCTATATC	4297
rs565624853	snp	A/G	0.00358779	0.0422022	intron-variant	KMT2A	GRCh38.p7	11:118507021	ATCATTGAAAGCCAA[A/G]CACAGTGGCTCATGT	4297
rs565630641	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118517025	GTTTTTCAATGTCTT[C/T]TTTTTTTAACCTAAG	4297
rs565666859	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118459831	AGCTAGGATTACAGG[C/T]GGGCACTACCACGCC	4297
rs565689196	snp	A/G	0.00199481	0.0315187	intron-variant	KMT2A	GRCh38.p7	11:118455127	AACTCTTGGGCTCAC[A/G]TGAACCTCCTGCCTC	4297
rs565695935	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118516225	ACATGGGGAAATGAA[A/G]TAGAGAGTGACACAG	4297
rs565762131	snp	A/G/T	0.00322365	0.0400184	synonymous-codon, missense	KMT2A	GRCh38.p7	11:118496292	AGAAGACAGTCCAGA[A/G/T]CTGAACCCACCCCCA	4297
rs565853636	snp	A/T	0.00398564	0.0444627	intron-variant	KMT2A	GRCh38.p7	11:118468018	AATCCTTTTTTTTTT[A/T]ATAGAGCAGGTTAAA	4297
rs565897936	snp	G/T	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118494050	ACCTGCTTGGATAAT[G/T]TATCATGATACAGCC	4297
rs565920886	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118487652	TAAACCATTTTACCT[A/C]TAAATATTTTAGTGT	4297
rs565946523	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522735	GATTCCTAGCACCTC[C/T]GGTGTCAAAAGGCTG	4297
rs565966604	snp	C/T	3.30109e-05	0.00406256	missense	KMT2A	GRCh38.p7	11:118505530	CAGACCTCAGTACCA[C/T]AGTAGCCACTCCATC	4297
rs566099865	snp	A/G	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118487548	TTTCTCTGTGTGTAT[A/G]TATTTTACAAAATAA	4297
rs566136013	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118438609	GTGCACACAAAATAT[C/G]CTGGGCAAACCCCTT	4297
rs566144398	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118449129	TGCCACCTAATGTGG[A/G]CTTCTCAGAATGTGA	4297
rs566169557	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118485063	TGTTTTGTTGGTATT[C/T]AGCAGGTACTATTCC	4297
rs566204598	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118466559	GTGGCTCACGCCTGT[A/G]AATCCCAGCACTTTG	4297
rs566212114	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118448250	TATTTGTAGCTTTTA[C/T]GTCCATTTTCAGTTG	4297
rs566231128	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118484508	TTTGTGAACTGACTG[C/T]AGAACATACATAATG	4297
rs566236120	snp	A/C/G			upstream-variant-2KB	KMT2A	GRCh38.p7	11:118436016	GGAAGCTGCTCTCCC[A/C/G]GGCTGTTCGATTCCC	4297
rs566274832	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118456497	GCACCTGCCACCACG[C/T]CCAGCTAATTTTTTG	4297
rs566297535	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118441499	AGGCCCTCTTGTTTG[A/G]CTAAATGTGTTGTCA	4297
rs566336234	snp	A/T	0.00597247	0.0543191	intron-variant	KMT2A	GRCh38.p7	11:118455670	CCCCTTATTATTATT[A/T]TTTTTTTTTATTTTT	4297
rs566379466	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118474551	AATGGAAAAGTAAGA[A/C]ATATATTTGAGGAAT	4297
rs566387625	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118465700	TGGATTGGCCCCCTC[C/T]ACAATTATAATATTC	4297
rs566394339	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118446385	AAGAAAAGATTTGCT[A/G]ACATACTCAGTACAC	4297
rs566449106	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118475866	TGTGATAGGAGCAGC[A/G]GCTCTTTAAAATCTG	4297
rs566455935	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118454522	GCCAGATGGCCTCTG[A/T]TGAAACTACTCCACT	4297
rs566487102	snp	C/G	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118437671	TCCTCATACAGCAGT[C/G]TCTTCCCCCCCCCGC	4297
rs566704051	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118511193	GCTCAAAGACGAGAG[C/T]TTACTAATGAGAGTA	4297
rs566740957	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118464230	TGGTTCAGCTTACAC[A/G]ATTCTGACTGAAAAA	4297
rs566748015	snp	C/T	0.000298493	0.012213	intron-variant, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118511948	TTCTTTATTTCCTTT[C/T]AGATGCCTGGAAGTC	4297
rs566889266	snp	A/G	1.65053e-05	0.0028727	synonymous-codon	KMT2A	GRCh38.p7	11:118504076	TGATGATGGGACAGA[A/G]AGTGATACTAGTGTC	4297
rs566939193	snp	G/T	0.0014985	0.0273314	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118472875	TCCACCGCCACCACT[G/T]CAGCCAGCCTCCAGT	4297
rs566953050	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118517124	TTGCCAGCTGGGCGC[A/G]GTGGCTCACGCCTGT	4297
rs566969260	snp	C/T	3.67458e-05	0.0042862	intron-variant	KMT2A	GRCh38.p7	11:118474353	TTAAAACTAACAGTT[C/T]ATTGAGCCCTTTCTA	4297
rs566987474	snp	A/C			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512786	TCTCCACCTTTGCCA[A/C]CACTTACCTGTTTTT	4297
rs567014227	snp	A/T	0.0460142	0.144533	intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118518944	ATTAGCCAGGCGTGG[A/T]GGCGGCGCCCGTAGT	4297
rs567046325	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118483134	GCTACTTGGGAGGCT[A/G]AGGCAGGGGAATTGC	4297
rs567076277	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118518553	TGGGAAGCTGAGGCA[G/T]GTGGATCACCTGAGG	4297
rs567109061	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118482283	AGTTAAATTGGAGGT[A/G]TTGTTTTAATTTCCT	4297
rs567109180	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118492172	ACTCTGAAGGTGATA[A/G]GGAGCCAGTGAAGCA	4297
rs567141219	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118517484	ATACAGTTGTGTTAC[A/G]TAGTGTTACATACCT	4297
rs567178722	snp	C/T	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118499072	CTTTTTGAATTATTT[C/T]GAAATGCAAAAGAAA	4297
rs567204017	snp	A/C	0.00119737	0.0244387	upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118526477	TCAAGAGCTCAACAG[A/C]TGACAAGCTTCTTTT	4297
rs567219056	snp	C/T	1.6563e-05	0.00287771	intron-variant	KMT2A	GRCh38.p7	11:118499797	AAATAAAATGACGCT[C/T]ATAATCTTCTCTAAT	4297
rs567239938	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118508692	TGCCACTGCACTCCA[A/G]CCTGGACAGCAAAGT	4297
rs567332519	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118452853	TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCG	4297
rs567395731	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118452144	AATCCTGAGCTTAAG[C/T]GATTCTACTCCCTCA	4297
rs567431339	snp	C/T	0.00199481	0.0315187	intron-variant	KMT2A	GRCh38.p7	11:118497816	ATTTCTGTGTGCCTC[C/T]CTCCATTAAAGAATT	4297
rs567460579	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118470406	CATGGTAGTTTCCTC[A/T]TAAGTTTTTTTTCAT	4297
rs567496858	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118459849	GCACTACCACGCCCG[C/G]CTAATTTTTGTATTT	4297
rs567519257	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118460093	GAAATTTTATCAGAT[C/G]AGTGGTATTACTAGA	4297
rs567528020	snp	C/G	0.00358779	0.0422022	intron-variant	KMT2A	GRCh38.p7	11:118479909	TTCTGTGTGGTGCTA[C/G]TCAGTGTTGGATTAC	4297
rs567575274	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118480757	AGCTTCAACCTCCCA[C/T]GCTCAAGCCATCCTC	4297
rs567582552	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118450369	CTTTTTCTGAAGCAG[G/T]GTGGGTGGAGGTCAC	4297
rs567590812	snp	C/T			synonymous-codon	KMT2A	GRCh38.p7	11:118505444	CATCAGCAATCCTCC[C/T]TCAGGCCTGCTTATT	4297
rs567611720	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118450602	TGTTATTGAAGAACA[C/G]AGAATTATTGTCTTA	4297
rs567645305	snp	A/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118458683	GTAATTATGTGAGCA[A/T]GTCTTTAAGGTGCAA	4297
rs567705139	in-del	-/A/AA	0.408394	0.230253	intron-variant	KMT2A	GRCh38.p7	11:118439158	AAAAGATACAGCAGC[-/A/AA]AAAAAAAAAAAAAAA	4297
rs567749358	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118446914	CTCCTGAATGTACAT[C/T]GTTACTGCTTCAACC	4297
rs567768672	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118467826	GGTTCCAGAATGTCT[A/G]TTCTTCATTCCTTAT	4297
rs567785359	snp	A/G	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118442061	GTGTTTTAATTGTAG[A/G]TCTCCTAATTAAGAT	4297
rs567819594	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118489730	GAAATGGGGTACTAA[A/G]TAATAGGTGTTGGGT	4297
rs567864448	in-del	-/A	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118446017	CCAAAAAAAAGAAAG[-/A]AAAAAAAGAAAAGTA	4297
rs567917986	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118440487	TTGACTAGAAGTTAG[A/G]CTGTTGTAATAATAA	4297
rs567974810	snp	A/G	0.00874735	0.0655527	intron-variant	KMT2A	GRCh38.p7	11:118449602	AAAAAAAAAAAAAAA[A/G]AGAGAAAAAAAATTG	4297
rs568001520	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118515292	ACACAACAAACTCCT[A/G]TTAATCCTTTAAGAC	4297
rs568014087	snp	A/G	0.0023933	0.0345097	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118524553	AAGTGCCAGCAGGGG[A/G]CTGGGAAAAGCACTC	4297
rs568037811	snp	C/T	0.00279162	0.0372561	intron-variant	KMT2A	GRCh38.p7	11:118469033	TTTAGGGTACATGTG[C/T]ACAATGTGCAAGTTA	4297
rs568080544	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118523625	AGGGAGAAGCACTTA[A/T]GACAAGGCTATTTTT	4297
rs568317760	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118456661	TATTTCTAAGTATGT[A/G]GGTATTCCTCAGAAC	4297
rs568368313	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118448165	TAAGTGGAGCTAAGA[A/G]AGAAATCTTAAACAT	4297
rs568375559	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118495020	CAATACATGTGTGGT[A/G]CAGCCATGTAGCTGG	4297
rs568398475	snp	A/G	0.00318978	0.0398085	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118513967	AAAAAAAGAAAAAGA[A/G]AAAAAAGTCTTGCTC	4297
rs568439743	snp	A/G	0.000598946	0.0172949	intron-variant	KMT2A	GRCh38.p7	11:118494403	TCTTCATTCGGGTGA[A/G]TGATATTACTAATTC	4297
rs568443458	snp	C/G/T	0.0103295	0.0711199	intron-variant	KMT2A	GRCh38.p7	11:118437684	GTCTCTTCCCCCCCC[C/G/T]GCCCCGTCTTACAGG	4297
rs568535933	snp	C/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118456381	TCTCACATTGTCACC[C/G]GGGCTGGAGTGCAAT	4297
rs568537763	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512925	CAAACTTATTAATAC[A/G]CTTGTTTTGAGCAAA	4297
rs568556248	snp	C/G			upstream-variant-2KB	KMT2A	GRCh38.p7	11:118435389	CGCGCACAGAGCTCG[C/G]CGCCGGCGGGCCCCT	4297
rs568582848	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521180	TTATTTTCTCAAGTA[C/T]ATGTCCCTCCTGGGG	4297
rs568620025	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118492417	GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC	4297
rs568621945	snp	A/G	0.0023933	0.0345097	intron-variant	KMT2A	GRCh38.p7	11:118501610	GCTGACTTTTTATTG[A/G]TTAATTTGTTTGATA	4297
rs568722128	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118464552	CTCAAAAAAAAAAAA[A/C]AAAAACCTAAAGTTG	4297
rs568728420	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118486588	GGTGGTAAAGAAAAT[C/T]CACGTCGGGTGCAGT	4297
rs568736836	snp	A/G			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522410	CCTGGGGCCCCTCCA[A/G]TTGTTTACTGTTAGA	4297
rs568800908	snp	G/T			synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473577	TTCCCTGACTCAGTC[G/T]GGGGAATCTGCAGAG	4297
rs568806539	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118483488	CAGTGAGCCGAGATC[A/G]CGCCACTGCACTCCA	4297
rs568835875	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118489137	CTGAGGGAGGAAAAT[C/T]GCTTGAACTTTGGAG	4297
rs568875049	snp	C/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512499	TTATTGCCAAATATT[C/T]CATTGTGTAGATATA	4297
rs568902701	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118462582	TTTATTTTTTGAGAC[A/G]GAGTCTCGCTCTGTC	4297
rs568950957	snp	C/T	0.0023933	0.0345097	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118436444	CGGGGCCCCGTGCCC[C/T]CCCCTCCGCCTCCCC	4297
rs569012271	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118435633	ACCGCGTCGTTAGCG[A/G]AGCACGCCGTGGCCT	4297
rs569024135	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118444439	TTTACAGAAGAAAGG[A/G]AGAATCTCATAATCT	4297
rs569070347	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118511090	CTTGAGGACTTTGAA[A/G]ACTTGAGGGAGTGAA	4297
rs569087465	snp	A/G	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118452901	CCTCCCAAAGTGCTG[A/G]GATTGCAGGCGTGAG	4297
rs569099153	snp	A/G	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118453648	GAGTTCCAGGCTTGT[A/G]TAGCCTGCTGCCAAT	4297
rs569336562	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118481257	ACCTCACTACCCTTC[C/G]CAGCCTCTCATAACT	4297
rs569463074	snp	C/T	0.00151475	0.0274787	synonymous-codon	KMT2A	GRCh38.p7	11:118502585	TGTTTCCTCAGTCTC[C/T]ACCACCGGGACCGCT	4297
rs569576909	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118457169	AGTCACTAATCTGCT[A/G]TAGCCTTCAGGATGA	4297
rs569629079	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118452110	TCACAGGCATAATCA[G/T]CATGTATTACAGACT	4297
rs569638812	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118508599	AGTTAACCAGGCATG[A/G]TGGTGCACATCCACA	4297
rs569640189	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118455430	GTTCATTATATATAC[C/T]ATTTCCAGAATAAAC	4297
rs569745081	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118464881	TTCTGGAGGACCAAA[C/G]AATGATAGCATCAGC	4297
rs569824221	snp	C/T	4.94238e-05	0.00497086	missense	KMT2A	GRCh38.p7	11:118506493	CAAGCCCTTCAGTGC[C/T]GGGTCCCACTAAACC	4297
rs569824650	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118458984	GTGCATCAGGAGTGA[C/T]TTTGATACTGTCTAT	4297
rs569831386	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118496746	GAATCGTTAAGAGCC[C/T]GAGTTCTGCCGCCTG	4297
rs569851377	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118525183	GCACAAAAGTGCAGA[C/T]TGAGGAATTGTGATG	4297
rs569861287	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118451774	TGGGATTATAGGTGC[A/G]ACCCACCATGCCCAG	4297
rs569870052	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118478703	GAAACATTGGAGATA[A/C]CTTGCATAAATATCT	4297
rs569888069	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118479740	TAGGGGTGAAGTATA[C/T]ATCAAAGCCACCAGA	4297
rs570008322	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118514198	TTACGTATTTGTTAT[C/T]AGTAAATATTTACTG	4297
rs570032741	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118467604	CTGCTAATTTGTCCT[A/G]AAAGTTATATATGTC	4297
rs570138929	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118441277	GGGATTCTGTTTGGT[A/G]ATTTTTAATATCAGA	4297
rs570198914	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118440223	GATGACTTTGCTGTT[A/T]GAACTCCCTTAGCCA	4297
rs570212246	snp	A/G	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118457464	TTTTAGTAGAGACAG[A/G]GTTTCACCATGTTGG	4297
rs570231000	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118475969	GGAGTGCAATGGCGT[A/G]ATCTTGGCTCACTGC	4297
rs570258431	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118481589	ATCTCTTTGATATAC[C/T]GATTTCCTTTATTTT	4297
rs570289240	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118448299	TTCAGAATAGCTCTT[G/T]TTAAGGCTGTCACTG	4297
rs570367506	in-del	-/G	0.00119737	0.0244387	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512809	TGTTTTTTGTTTTTT[-/G]TTTTTTTATTTTAGA	4297
rs570387924	snp	A/C	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118437681	GCAGTCTCTTCCCCC[A/C]CCCGCCCCGTCTTAC	4297
rs570445507	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118447212	ACCTTATGTCGTGGT[A/G]CTTTTGAAATGTGTC	4297
rs570449576	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118437058	CATCTCGGGGTCCCT[C/G]ACCCGGGGCGAATGG	4297
rs570459440	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118486226	CACTGAGTGAAAAGA[A/G]CAGGTTACAAGATAA	4297
rs570507050	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118446663	TGTTCCTGCTGTCCT[A/C]GTTTAAATTTCCATT	4297
rs570752376	snp	A/G	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118455321	ACCTGGCAATACTCA[A/G]TAAATACTTATTGAA	4297
rs570790752	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521637	TGTCTGAGTGGCTCC[C/T]AGTATCAGAAGCAAA	4297
rs570830965	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118501928	GTAATTCTTTCAGGC[A/G]ACTTTATCTTGGTGA	4297
rs570922084	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520995	AAGTGAGGATTTTAC[A/G]GACACTATTTATTGA	4297
rs570923787	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118479101	GTATTACAAACAATC[C/T]AATTATACTCTTTCA	4297
rs570977342	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118482691	GAGGTGGGAGGATTG[C/T]TTGAGGCCAGCAGTT	4297
rs571064203	snp	C/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118509824	TGTTATCTATAAATG[C/G]GAATAATAAACCAAC	4297
rs571084708	snp	C/G	0.00274522	0.0369469	intron-variant	KMT2A	GRCh38.p7	11:118447606	CATCCCCTTACTTGA[C/G]TGTTGTTTCCATTTC	4297
rs571088938	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521736	ATCTAGGAAATCCTC[A/G]TGGAAGCATCTTGAA	4297
rs571101678	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118474409	CAATTACATCCAGTT[A/T]TGAGAACCAAGAAAA	4297
rs571125125	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118518971	TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGTAGG	4297
rs571191158	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118492324	TTATAGTAATCAACT[A/G]GAAAAACACTTTCTG	4297
rs571208488	snp	A/C			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512235	GTATAACCACCACTA[A/C]TCTATAATTCTAGAA	4297
rs571230532	snp	A/G	3.30901e-05	0.00406743	missense, intron-variant	KMT2A	GRCh38.p7	11:118472651	TCTGAGGAGATTCAG[A/G]TACTTCCTGAGGAGC	4297
rs571250390	snp	C/G	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118500527	CACACAAACCAGATT[C/G]CACTAGCATTCAGCA	4297
rs571325301	snp	C/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118516836	ATACGTCTCTGCCTT[C/T]CTCTGCTGTGAGCTC	4297
rs571333863	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118434903	CCGCTCTGCACAAAT[A/G]TTTCGCCAGTGGAGG	4297
rs571382642	in-del	-/T			intron-variant	KMT2A	GRCh38.p7	11:118465922	TTTTGTTTTGTTTTG[-/T]TTTTTTTGGTAACAT	4297
rs571449143	in-del	-/AAAAC	0.00637825	0.056111	intron-variant	KMT2A	GRCh38.p7	11:118466807	TGCCTCAAAAAAAAC[-/AAAAC]AAAACAAAACAAAAC	4297
rs571480243	snp	C/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118462232	GTGCTGGGATTACAG[C/G]TGTGAACCACCATGC	4297
rs571514712	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118446854	TTTCAGATTCTCAGC[A/G]CTGCATGATCTTGCT	4297
rs571579179	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118442248	AGAAGGGGGAAGCTT[C/T]GTGACTATCACTACT	4297
rs571632587	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118457744	CCCCCACCAGCTTTA[C/T]CATCCTTCGAAAGAT	4297
rs571715079	snp	A/G	1.67248e-05	0.00289173	synonymous-codon	KMT2A	GRCh38.p7	11:118488751	TGGAAGGCAACATCA[A/G]GCTACAAAGGTACAA	4297
rs571770215	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118439262	CATTTTAGCCCCATG[C/T]ATATTTGAGTTTAAT	4297
rs571779280	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118497863	GGTTATCTTCACTGG[A/T]AAAGCTAATGCCGAG	4297
rs571780725	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118498778	TTCACTCTTGGTGTT[G/T]TACATTCTGTGGGTT	4297
rs571884060	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118438441	GTTCGAATTGTAGAG[G/T]GGGGAGGATGGCATG	4297
rs571901678	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118496111	ATAGATGATGAGGTA[A/G]CGTAACTCTGAACAC	4297
rs572121925	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118490548	GACATTATTTTAGTT[A/G]CTACCCAAACATTTT	4297
rs572129477	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118457899	TTAATTTACTCATCT[A/G]TTTTTAAGATTAGCA	4297
rs572129912	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118456772	ATATTCATTGAGTCA[A/G]ATGTGTTTTCTTCAG	4297
rs572191837	snp	C/T	0.00438332	0.0466095	intron-variant	KMT2A	GRCh38.p7	11:118458337	CAAGCCATCCTCCCT[C/T]CTCGGCCTCCCATTG	4297
rs572230921	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118514601	GCATGCTACCACACC[C/T]GGCTATTTTTTGTAT	4297
rs572253387	snp	A/G			upstream-variant-2KB	KMT2A	GRCh38.p7	11:118435642	TTAGCGGAGCACGCC[A/G]TGGCCTCAGTGCCCG	4297
rs572292854	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118523088	ACAGAATTTGGAAAC[A/G]TTTTCATAAAGCTCC	4297
rs572316333	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118486641	ACTTTGGGAGGCTGA[C/T]GCAGGAGGACCGCTT	4297
rs572363330	in-del	-/C	0.00318978	0.0398085	intron-variant	KMT2A	GRCh38.p7	11:118475374	GTCATGTAGTAGATG[-/C]CTATTTATGGCAGCA	4297
rs572386719	in-del	-/T	0.00199481	0.0315187	intron-variant	KMT2A	GRCh38.p7	11:118441716	ATTAGAAATTCAGTC[-/T]TTAGAACTTTTCTTC	4297
rs572442254	snp	C/G	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118476152	TCAGGTGATCTACCC[C/G]CCTCGGCCTCCCAAA	4297
rs572445603	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521212	ACTAACAGACCAGGA[A/G]AACTTATTCATGTAT	4297
rs572481234	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118437740	CCGGGAATTACTCTA[C/T]CTTCACTCCACCCTT	4297
rs572507220	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520602	GTTACAGTGAGCCGA[A/G]ATCGCACCACTGGAC	4297
rs572557316	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118493445	TGTCTTAAAATAGTT[A/C]TTTTATTTGGCTTTC	4297
rs572595669	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118437350	TCTCTGGGCAGATGT[A/G]TTACTCCTAGGGCAG	4297
rs572616851	snp	A/G	0.0023933	0.0345097	intron-variant	KMT2A	GRCh38.p7	11:118502202	AGGTTGCAGTAAGCC[A/G]AGATCGCACCACTGC	4297
rs572783697	snp	C/G			missense	KMT2A	GRCh38.p7	11:118481789	AGTGTTGTGAAGAAC[C/G]TGGTGGACTCTAGTC	4297
rs572793420	snp	C/T	3.43077e-05	0.00414158	synonymous-codon	KMT2A	GRCh38.p7	11:118491914	ACTACCAGCCATTTG[C/T]TACGCTACCGGCAGG	4297
rs572798917	snp	A/C	0.00318978	0.0398085	intron-variant	KMT2A	GRCh38.p7	11:118475245	GCCAAATATTTTTAC[A/C]AAGACCAGCATTTTT	4297
rs572843360	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118463642	AACTATTCTACAGCC[A/G]GTTTAGACACTTAGG	4297
rs572862641	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118454117	TATAGTCTCTTGGTT[A/G]GAGTTGCTTATGTTA	4297
rs572907081	snp	A/T			intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118519094	AAAAAAAAAAAAAAA[A/T]AAAAAGAAAATTAAA	4297
rs573028268	in-del	-/TTTTTA	0.0166325	0.0896639	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118514626	TGTATTATTATTATT[-/TTTTTA]TTTTTATTTTTATTT	4297
rs573070638	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118457973	CGTAGCCTAGGAATG[A/G]CCGATATATATTTTA	4297
rs573088930	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118461790	ATATTACTGTAGTCT[C/T]TTGATTTCTAGATAA	4297
rs573147931	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118460614	TAAGCAAAATTTTTT[A/T]TTCCAGAATATGAAT	4297
rs573207631	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118510333	ATACAGATTATGTTT[G/T]CAACATTGCACACAC	4297
rs573217200	snp	A/G	0.00199481	0.0315187	intron-variant	KMT2A	GRCh38.p7	11:118443787	AATTATTGCTGCAGC[A/G]GTACCCTGTGAAGTA	4297
rs573280197	snp	C/G	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118462625	GTGCAGTGGTGCGAT[C/G]TCGGCTCACTGCAGG	4297
rs573334832	in-del	-/A	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118488025	CTCTACTAAAAATAC[-/A]AAAAATTAGCCAGGT	4297
rs573354552	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118497827	CCTCCCTCCATTAAA[A/G]AATTATAGTTGCTTT	4297
rs573432491	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118471428	AAACTTTTTATTATC[A/T]TTTTGTATCAAAAAA	4297
rs573544692	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118492090	TAGGACCTTCTTTAG[A/C]GTAAGAAATAGGAAG	4297
rs573640982	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118525463	TTTACACCAATAACA[A/G]GAATTAAGGGGGAAG	4297
rs573709036	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118442489	GGTTTATGAAACTTG[A/C]TGAGTAAAATATTGT	4297
rs573731379	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118507919	AGTGAGCTGAGATCG[C/T]GCCACTGCACTCCAG	4297
rs573746510	snp	A/C	0.00199481	0.0315187	intron-variant	KMT2A	GRCh38.p7	11:118441946	TGCAGACTCTATACC[A/C]ATTGCCTCCCTTACC	4297
rs573771484	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118488357	ACTCTTAGGTCACTT[A/G]GCATGTTCTGTTAAA	4297
rs573832938	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118497299	TGAGCCACCGTGCCC[A/G]GCCAAAAGCTTTTAA	4297
rs573834204	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118516447	CACCAGCTGAGCAAC[A/T]CAGTGAAACTCTCTT	4297
rs573860827	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118507051	TCTGTAATCCCAGCA[A/C]TTTGGAAGGCTGAGG	4297
rs573896393	snp	C/G	3.30628e-05	0.00406575	intron-variant	KMT2A	GRCh38.p7	11:118468869	ATTAAGTGCATGGTG[C/G]CTTTTAAGTTTTGTT	4297
rs573921515	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118515736	CTGTTGCCCAGGCTG[C/G]AGTGTGTAGTGGTGC	4297
rs573953725	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118469437	TATGTGAAACATTTT[C/T]ACCTGATTCTTGAAA	4297
rs573983121	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118495353	AATAGAGACTGGGTT[G/T]CACCATTTTGGCCAG	4297
rs573987920	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118452259	TAGCTTTTTCAGTCA[C/G]GCATGGTGGCTCACA	4297
rs573998220	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118459151	CTCAGCTCACTGCAA[A/C]CTCTGCCTCCTGGGT	4297
rs574019586	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118497185	AATTTTGTATTTTTA[C/G]TAGAGACGGAGTTTC	4297
rs574061287	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118442736	CTATTTCTTGAGATT[C/T]TCAGGAATTGTCTAG	4297
rs574062078	snp	C/T	0.0023933	0.0345097	intron-variant	KMT2A	GRCh38.p7	11:118478261	AGGTTGCTTATTTAT[C/T]CCTAGTTTGTTGCAG	4297
rs574069002	snp	G/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118458135	GTCACCCAGCCTGGA[G/T]TGCAGTGTCTCGATC	4297
rs574115720	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118448253	TTGTAGCTTTTATGT[C/T]CATTTTCAGTTGTCA	4297
rs574151523	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118477231	GAAGGAGCAGGGGAA[A/G]GAAGGCAGAATCTTC	4297
rs574253929	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118442903	TATCTTTTATTAAGA[A/G]AAAGGAATCTTAAGT	4297
rs574267581	snp	A/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118466057	AGAGATAATTTTTTT[A/T]TTTTAAAATTACTTT	4297
rs574271491	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118483024	GATCACTTGAGGTCA[A/G]GAGTTGGAGACCAGC	4297
rs574281253	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118438902	GCCTCTTTCTGCTCT[A/G]TCTCCACCTCCTTTT	4297
rs574340225	snp	A/G	0.0023933	0.0345097	intron-variant	KMT2A	GRCh38.p7	11:118448471	TTTTTAGATATGTTG[A/G]GTTGCAGAAAGCATT	4297
rs574366841	snp	A/G	0.0023933	0.0345097	intron-variant	KMT2A	GRCh38.p7	11:118437904	GGGGGCCCCTGTGAG[A/G]GGAGGTGTTTGTTGG	4297
rs574564055	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522958	GGTTGTAGGGGAGAC[C/T]GACTGCCTGCTCAAG	4297
rs574655269	snp	G/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118485456	GGAGGTGAAGGGAGG[G/T]TGTCTGTTTTTTAGC	4297
rs574692364	snp	C/G			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118523903	CCACTCCCCTCCTTC[C/G]CCTATTGAAGCTCCT	4297
rs574751268	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118484656	ATTTTCGCAATATAT[C/T]CAATATGAATTGAAC	4297
rs574802088	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118437194	CCTGACCCTTCCCCA[A/C]ATCCCTTGGCACAGA	4297
rs574964465	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118445835	TGGTGAAACCCTGTC[C/T]CTACTAAAAATACAA	4297
rs574975018	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118492594	TGAGGCAGGAGAATG[A/G]CGTGAACCTGGGCGG	4297
rs574985085	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118502026	GGGAGGCCAGGGCAG[A/G]TGGATCACCTGAGGT	4297
rs575038604	snp	C/T	5.17862e-05	0.00508826	intron-variant	KMT2A	GRCh38.p7	11:118501195	GGGCACAGTGGCTCA[C/T]GCCTGTAATCGCAGC	4297
rs575044892	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118453311	GGTTCTCAAGGAGCT[C/T]TATTTTACCAGATTG	4297
rs575055890	snp	A/C	0.00358779	0.0422022	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520493	CTATCTCTACTAAAA[A/C]TACAAAAATTAGCCC	4297
rs575071761	snp	C/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519457	GATCTGTATCAGCAT[C/G]ATTTTAATGGCTATC	4297
rs575133150	snp	G/T	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118500196	AAGATTCCTCCAAAT[G/T]CCATTCATCTCCATG	4297
rs575198886	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118461268	TGAATAACGTGAATT[C/T]AGTGGTAAAGGTATG	4297
rs575225519	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118463346	GCTTGAGCTGTCAAT[C/T]ATTGTAGCATTTGGA	4297
rs575288656	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118461529	GATCTAGTCTCCAAG[A/G]ACATCAGTGTCAGCA	4297
rs575361538	in-del	-/T	0.00159712	0.0282137	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118524703	TGTATTCCTATTTTT[-/T]TTTAAAGAAAAAAAA	4297
rs575386760	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118490427	TGTCTTGTTAGTTTA[C/T]ACGGGAAGTGTTAAG	4297
rs575476436	snp	C/T			synonymous-codon	KMT2A	GRCh38.p7	11:118501089	AGAGCCGGATATCAA[C/T]AGCACTGTTGAACAT	4297
rs575512145	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118435019	CTGCTCACAACGACC[C/G]TCTCCCTCCTTCCCA	4297
rs575537229	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118442715	AGAATACCCTTGTAG[A/G]CTCCACTATTTCTTG	4297
rs575633348	snp	G/T	0.000798403	0.0199641	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118517873	TATCTAGAGACAACA[G/T]TCTTTTTGTTTGTTT	4297
rs575694710	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, downstream-variant-500B, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118526953	AGGTGGCATCACTAA[A/G]TTATTCCCTGTAGCC	4297
rs575841329	snp	A/C	6.59729e-05	0.005743	intron-variant	KMT2A	GRCh38.p7	11:118480267	AAAGGTCTTCCCCCA[A/C]ATGCTCCTTGCTTAA	4297
rs575849802	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118461623	AAGGAAAAGTGTGTG[A/T]TGAATGGTTGCCTGA	4297
rs575850891	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118479156	TTATTATTTACTACA[A/G]TCACCCTGTTGTGCT	4297
rs575912762	snp	A/G	0.00199481	0.0315187	intron-variant	KMT2A	GRCh38.p7	11:118438254	CCAAGGTGGATGAAG[A/G]GTCAGAGCGTTGCCC	4297
rs575919583	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118488050	CCAGGTGTGGTGGCA[C/T]GCGCCTGTGATCCCA	4297
rs576117110	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118450630	TTAGCGCTCTTTAAT[C/T]CCAAGTGACCTTTTT	4297
rs576120081	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118447416	GAGAACTTAAGACTA[C/T]GAACAGAATATTTGG	4297
rs576142171	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118497193	ATTTTTAGTAGAGAC[A/G]GAGTTTCTCCATGTT	4297
rs576148041	snp	C/T	0.000798403	0.0199641	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118516288	CTCTTGATGAGGCAA[C/T]ATTTGAGCTTAGACC	4297
rs576148887	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118449859	ATAAGAACAACAAAC[A/G]GAAGAAAAAAACTGA	4297
rs576203263	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118507114	TCAGTCTGTGCAACA[C/T]AGTAAGACCCTGTCT	4297
rs576210370	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118457975	TAGCCTAGGAATGGC[C/T]GATATATATTTTAAT	4297
rs576240145	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118524017	GGAGACGGCAATCTT[C/T]ACATTTCCCTCATCT	4297
rs576332588	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118523150	GATTTTGTAGGAGAG[C/G]AAAAAGATTATTTAA	4297
rs576385136	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118513208	ATGATCTTAGCACTG[C/T]ACTCCAGCCTGAACG	4297
rs576392832	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118461088	ATTTTTCTAATATAC[C/T]TTATATTTTATACAC	4297
rs576395969	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118485662	CACTTCAAACACTTA[G/T]GGATATAATTAGATA	4297
rs576424054	snp	C/T	0.00159617	0.0282053	intron-variant	KMT2A	GRCh38.p7	11:118468171	AAACGCTGCTGCCCA[C/T]CATTAAGTCTCTTAT	4297
rs576455381	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512557	CAGTGGACATTTGGG[G/T]TTTTTCTATTTTCTG	4297
rs576483315	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118468514	GAAATTAGGACTATC[C/T]TCTGTGTACTATGCA	4297
rs576485905	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118477943	CAGTACTCCCTTGGA[A/T]CTAATGCCACATTTC	4297
rs576531663	snp	C/T	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118495244	GCTCACTACAACCTC[C/T]GCCTCCCTGGTTCAA	4297
rs576547151	snp	C/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118464889	GACCAAAGAATGATA[C/G]CATCAGCTTATTTGA	4297
rs576550650	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118485717	GAAGTGTTCATTTCA[A/G]TATTGCTCATAATAA	4297
rs576608575	snp	A/C			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520232	GGTAAGGAGTGAGGA[A/C]TATAAGGTACAGAGG	4297
rs576608678	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118475359	GGTTTTAAAAAAATC[A/G]TCATGTAGTAGATGC	4297
rs576669234	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118474687	GTTTGATGTAATTAA[A/G]CCAGGGACTTAATTG	4297
rs576707091	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118438836	GAGCAAGGAGGACAT[A/G]ATGGGGGCGTGTTCC	4297
rs576754943	snp	A/T	0.00993419	0.0697739	intron-variant	KMT2A	GRCh38.p7	11:118455676	ATTATTATTATTTTT[A/T]TTTATTTTTATTTTT	4297
rs576764559	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118447069	CGTCTCCCATGGTTC[A/G]ACTCAGATCCCCAGA	4297
rs576770217	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118437817	AGTCCACTGTCCCCT[A/G]GGCTTAGAGAAGAGC	4297
rs576824930	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118436091	GCTGCAGGCGGCCCG[A/G]CTCCCTACGCCTCCA	4297
rs576853947	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521471	TGCTGTAGAAAGGGA[C/T]CAGTATGACCCCTGG	4297
rs576884235	snp	A/G	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118445729	AGTTTTGGGTTGGGC[A/G]CAGTGGCTCACGCCT	4297
rs576887016	snp	C/G	0.00279162	0.0372561	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118435211	CAAGTTCTCCCGACA[C/G]AAACCCCTCCCTACC	4297
rs577009687	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118484572	GAAGTAATTCCTTCA[C/T]ATGGAAAGTATCAAA	4297
rs577070092	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118492907	TCATTTTTAACTTTC[C/T]TTTTCTATTTGAGAA	4297
rs577138679	snp	C/G	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118492548	GCCAGGCATGGTAGC[C/G]GTCACCTGTAGTCCC	4297
rs577327437	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520227	TGCCTGGTAAGGAGT[A/G]AGGAATATAAGGTAC	4297
rs577393117	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519395	CATAGTTTGGTGGCA[C/T]GCTTTTTTCACTTAG	4297
rs577410998	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118511472	CAGACAGGAAAAGAT[C/T]ACAGAATCTTGGGTT	4297
rs577449342	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118508784	GCAGCTTATTTTTTA[A/G]TTTTAGTTAAGCCAG	4297
rs577470983	snp	A/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118510409	TTTTGCCATTCCCTC[A/T]TGCGCCTTCTGTGCC	4297
rs577471092	snp	A/C	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118464812	AGACTGTTTAAGAGC[A/C]AAGGTCATGGCAACA	4297
rs577511232	snp	C/T	0.00119737	0.0244387	intron-variant	KMT2A	GRCh38.p7	11:118508010	TCACATTGATTTTTG[C/T]TTTCTTGCCAAAGTT	4297
rs577532482	in-del	-/A	0.00557542	0.0525036	intron-variant	KMT2A	GRCh38.p7	11:118486082	GCAAGACTCCGTCTC[-/A]AAAAAAAAATAAAAG	4297
rs577575320	snp	A/C	0.00159617	0.0282053	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118517795	CAGTGAGCTATGATC[A/C]TGCTACTGCACTCCA	4297
rs577598609	in-del	-/G	0.00119737	0.0244387	utr-variant-3-prime, intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118524811	GGCCAGTCAGGGGGT[-/G]GGGGGAACTCAGCTA	4297
rs577619340	snp	A/C/G	6.5982e-05	0.00574345	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473472	GCTCTCACCTCTCAC[A/C/G]CCCCCGTCTTCTGTC	4297
rs577621721	snp	C/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118513811	GCATGATGGCTCATG[C/T]CTGTGGTCCCAGCTA	4297
rs577680799	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118482326	GAGTTTAAATAGTTT[G/T]TTTTTTTTTTTTCTA	4297
rs577681070	snp	G/T	3.32474e-05	0.00407708	missense, intron-variant	KMT2A	GRCh38.p7	11:118471914	GAAACAAAGAAGATA[G/T]CCTGAAAAAAATTAA	4297
rs577726462	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118517042	TTTTTTAACCTAAGA[A/G]TTCACAGCAATCTAG	4297
rs577756852	snp	G/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118481646	GGATCATATGGTGGC[G/T]CTGTAATTCTATTTT	4297
rs577848493	snp	A/C	0.00318978	0.0398085	intron-variant	KMT2A	GRCh38.p7	11:118450789	CCTGCCCCTGACAAT[A/C]TGTTCACAAGAGAAT	4297
rs577931627	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118453252	CCTCAACTACTCCAG[C/T]TGGGCTTTTATCCCC	4297
rs577942705	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118500459	GCTCCAACTTACTCT[C/G]TATTCCTATTCCTAT	4297
rs577950836	in-del	-/T	0.126219	0.217206	intron-variant	KMT2A	GRCh38.p7	11:118450214	TTCTTGAGTTTTTGG[-/T]TTTTTTTTTTTAAAG	4297
rs577952533	snp	G/T	0.000798403	0.0199641	intron-variant	KMT2A	GRCh38.p7	11:118460290	ATAGAAGGAAGAATA[G/T]ACTTTTTCTTTTTTC	4297
rs577994678	snp	C/T	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118459373	TGCCAGGCCCTGATT[C/T]TTCATAAGACTAAAA	4297
rs577998661	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118456319	TAGTGAGACCTCATC[G/T]CTACTAAAAATTTAA	4297
rs578023817	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118525629	AAAAAAAGGAAAAAA[A/G]AATACAACACACACA	4297
rs578039295	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118469622	TTCTGTATAGGAGAA[A/G]GCTATGTATCTTTTG	4297
rs578058102	snp	A/G	0.000399281	0.0141238	intron-variant	KMT2A	GRCh38.p7	11:118451122	CATTTATCAAAGAAC[A/G]TCTTTTATACTCTAG	4297
rs578082162	in-del	-/T			intron-variant	KMT2A	GRCh38.p7	11:118452641	TTTTTTTCTTTCTTG[-/T]TTTTTTTTTTGAGAT	4297
rs587783676	in-del	-/GA			frameshift-variant, intron-variant	KMT2A	GRCh38.p7	11:118473832	GGAGTCAAGGAAAGA[-/GA]AAAGGAAAAAGGGAT	4297
rs587783677	snp	A/T			missense	KMT2A	GRCh38.p7	11:118488707	CTGGAAAATTGGTGT[A/T]GTCGTCGTTGCAAAT	4297
rs587783678	snp	C/G			stop-gained	KMT2A	GRCh38.p7	11:118468800	TCTTAGGTTTTGGCT[C/G]AGATGAAGAAGTCAG	4297
rs587783679	snp	G/T			stop-gained	KMT2A	GRCh38.p7	11:118503723	GGCCCCAAACCTCAG[G/T]AGGATGGCTCTTTTA	4297
rs587783680	snp	C/T			stop-gained	KMT2A	GRCh38.p7	11:118503987	TCAGGTGGAGAGGAA[C/T]GACTGGCATCCCATA	4297
rs727503777	snp	C/T			stop-gained, intron-variant	KMT2A	GRCh38.p7	11:118473392	GTGTTTAGTCCTATT[C/T]GATCTGAACCAAGAT	4297
rs745443430	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118468385	CTGTAGACTTAAATA[C/G]TTTTTGAAAAGCATT	4297
rs745636858	snp	A/T	1.64735e-05	0.00286993	synonymous-codon	KMT2A	GRCh38.p7	11:118505849	CACAGCGGCAGGCAC[A/T]TCAACAATAAGCCAG	4297
rs745869642	in-del	-/TC			intron-variant	KMT2A	GRCh38.p7	11:118488386	ATCTTGTATTATATT[-/TC]TATTTTGTTACTTTC	4297
rs745922442	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118486599	AAATCCACGTCGGGT[A/G]CAGTGGCTCACGCCT	4297
rs746200920	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118463237	TGCTGGGATTACAGG[A/C]ATGAGCCACTGCACC	4297
rs746252390	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118457858	AGTGTCTTCCTCTAG[C/G]ATAGCAGGCAACATA	4297
rs746472635	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118437664	CGGTGATTCCTCATA[C/G]AGCAGTCTCTTCCCC	4297
rs746789821	snp	C/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118513500	AACATTTGTTCATTT[C/T]ATGTGACAGGTACAT	4297
rs747019062	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118452063	AGAGACGAGGTCTCA[C/T]TATGTTACCTGCGCT	4297
rs747091987	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118489005	GTGGGCGGATCACTT[A/G]AAGCCAGGAGTTCGA	4297
rs747397870	in-del	-/G			utr-variant-3-prime, intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118525077	GGGGGAATAAGCGAA[-/G]GTTTCCCTACAAGAG	4297
rs747410771	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118463930	CCCTATCAGAGCAAC[A/G]TAAGTTCTGCTAAAA	4297
rs747699848	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118495929	TCGTCACCCATTTCC[C/T]TCTAGATGCAGATGA	4297
rs747876903	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118437935	GGGACTGAGGCAGCA[A/T]CCTCCCAGGGGAAGC	4297
rs748227357	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118456809	ATACCCTTTAGACAA[C/T]GTGGATAAACATTTC	4297
rs748254599	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118492455	GAGGCCGAGGCGGGC[A/G]GATCACGAGGTCAGG	4297
rs748337387	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118449254	TATTCCTAAAAAATA[A/G]TAAGTCAAAATTGTG	4297
rs748533574	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118490009	CTTTTTGCCTCATTA[C/T]TAGGAAATCATCTCA	4297
rs748775392	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118467396	AAAAAAAAAAAATTA[C/T]AATACTTTTTCAGAT	4297
rs748830529	snp	A/G			missense	KMT2A	GRCh38.p7	11:118505329	GCTTGCCAACTTCTC[A/G]ATCTTTGTTCCCTTC	4297
rs749059930	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118486040	GTGAGCCGAGATCGC[C/G]CCACTGCACTCCCGC	4297
rs749129781	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118438664	TTTAGATTTACGGAA[A/G]GATCCTGGGAAGAAG	4297
rs749354451	snp	G/T			missense, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519714	GTCGAAATTACAAAT[G/T]CCGTTTCCACAAGCC	4297
rs749587086	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118457459	GTATTTTTTAGTAGA[A/G]ACAGGGTTTCACCAT	4297
rs749647502	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118495228	CAGTGACATGATCTC[A/G]GCTCACTACAACCTC	4297
rs749700173	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118492975	TAATCATTCAGTACC[A/G]TCTTTATTAATTTTA	4297
rs749867464	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118477442	TTCTCGATTTTAGAT[G/T]AGACTTTTGTTTTCA	4297
rs749915665	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118518347	ATGTTGTTTTCATAA[A/G]ATAAAAATAAATAAA	4297
rs750998886	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118441533	TTGTGAATTCCAGAC[C/T]ATCCAAAAGAGAAGT	4297
rs751084487	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118485253	AAATAAGAGAAAAAA[A/T]TATACAGTGGTCTAT	4297
rs751137667	snp	C/T			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522386	GAAAAGATCCATGAT[C/T]GGCTTTCTCCTGGGG	4297
rs751141744	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118481187	ATACTAGATCTCATT[A/C]ACTTCTATCTAGCTA	4297
rs751640163	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118492290	GAGCCTAGAGGCAGG[A/C]TTCGTAGTTAGGGGA	4297
rs751867095	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118476000	AACGTCCGCCTCCCA[A/G]GTTCAAGCAATTCTC	4297
rs751892915	snp	G/T			intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118511431	TGATGTGGAGTGATG[G/T]AAGAAATCCATGTGG	4297
rs751944265	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118507871	AGGAGGCTGAGGCAG[C/G]AGAAGGGCGTGAACC	4297
rs752356525	snp	C/G			upstream-variant-2KB, downstream-variant-500B, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118527115	CTTCTACATAGCTCC[C/G]CTGTTTCATCCAAGG	4297
rs752518405	snp	C/T			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522867	AGTAGGAGCGGCTTC[C/T]CTCTCCCATTCCCTC	4297
rs752791595	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118497090	GCTCACTACAACCTC[C/T]GCCTCCTATGTTCAA	4297
rs752843399	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118494940	GTTATAAGCAATTGC[C/T]TTTTTGTTCTTTACT	4297
rs753016009	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118479539	GAAGTAGTTCTGTGC[C/T]TTGGTTTGGTCTGAC	4297
rs753071205	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118476442	CTCAAGTGATCCTCT[C/T]GTCCCAGCCTCCTGA	4297
rs753264100	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118508687	GTGATTGCCACTGCA[C/T]TCCAGCCTGGACAGC	4297
rs753313583	snp	A/T			intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118511884	CAGTGCTTGTGCACA[A/T]CATTGGTATTAAGAA	4297
rs753487084	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118491049	CTTGAGACTGCAGAT[A/G]TGTGAACATTCCACA	4297
rs753582614	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118445897	TATCCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	4297
rs753637509	in-del	-/CTTG			intron-variant	KMT2A	GRCh38.p7	11:118488374	CATGTTCTGTTAAAT[-/CTTG]TATTATATTTATTTT	4297
rs753925021	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118465528	CATAAATTATTTATT[A/C]CTTACAGTGCTCAAA	4297
rs754165571	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118441140	TTCTGAGTTTATTTC[-/A]AAAGTCAGAGTCAAG	4297
rs754202278	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118437235	GGGGTTTCCCATCCC[A/G]GGACTGAACCCCTCC	4297
rs754584211	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118485575	GATTAGTTACAATCT[G/T]TCTTTCTGAGGGAAT	4297
rs754861168	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118456724	ATATTCTTTCCCTGG[A/G]TGACTGAATTCATAC	4297
rs755071219	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118492396	TTAGAAGAACCACAC[A/G]GGGCCGGGCGCGGTG	4297
rs755723799	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118445570	GGTCTACAGAGATCA[A/G]TGCAAGTAACCATTT	4297
rs755741033	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118487838	CTGGATTATCCTAGT[G/T]AGTATTTTTGAAAAT	4297
rs755778811	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118442194	TCTCTTTCCATTCTT[C/T]CTCTGCCAAGGTGGA	4297
rs755922083	snp	G/T			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522922	CTGTCTTCATGCCAC[G/T]GCTTTCCCATGCTTC	4297
rs756050267	snp	C/T			intron-variant, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519437	AAACATTTTCCATAT[C/T]GATAGATCTGTATCA	4297
rs756212110	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118462053	CTGCCTCCCAGGTTC[A/G]AGTAATTCTCGTGCC	4297
rs756454275	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118437176	GCCCCCCGCTCTCCT[A/C]CCCCTGACCCTTCCC	4297
rs756562807	snp	A/G			missense	KMT2A	GRCh38.p7	11:118476890	CTGTTGCCCTTGGCC[A/G]AAAACGAGCTGTGTT	4297
rs756582747	snp	C/T	1.65285e-05	0.00287471	synonymous-codon, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118511955	TTTCCTTTCAGATGC[C/T]TGGAAGTCATTGACA	4297
rs756873110	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118450695	ATTTAAACAGTTTCA[A/G]TCTCTTCCTATCTGT	4297
rs757048058	in-del	-/T			intron-variant	KMT2A	GRCh38.p7	11:118488379	CTGTTAAATCTTGTA[-/T]TTATATTTATTTTGT	4297
rs757178260	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118486047	GAGATCGCCCCACTG[C/T]ACTCCCGCCTGGGCG	4297
rs757370068	snp	C/T			missense	KMT2A	GRCh38.p7	11:118501737	TCACCAGACCGACCT[C/T]CTCATTCACAAACCT	4297
rs757449280	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118465533	ATTATTTATTCCTTA[A/C]AGTGCTCAAATAAAA	4297
rs757712041	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118480913	CTCAAGCAATCCTCT[C/T]GCCTTGGCCTCCCAA	4297
rs758042410	snp	G/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118518500	ACTTTAGTGAGGCTG[G/T]CTGGGTGCTGTGGCT	4297
rs758081290	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118513106	ATATTAGCCGGCACC[A/G]TGGCATGCACACCTG	4297
rs758187152	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118455982	GCATGAGCCACTGTG[C/T]CCAGCCTTGGCTACA	4297
rs758242286	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118450942	CTTACTGATTGAGCA[A/G]CATTATTTTTATATT	4297
rs758334108	in-del	-/C			intron-variant	KMT2A	GRCh38.p7	11:118488391	GTATTATATTTATTT[-/C]TGTTACTTTCTATTT	4297
rs758501523	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118470573	AAGGAGCTGTGAATC[C/T]TTAATCTATTAAAGG	4297
rs758803222	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118498304	GGATGAGTCTATAGA[A/G]GAGACGGTAAACGTC	4297
rs759510518	in-del	-/AG			intron-variant	KMT2A	GRCh38.p7	11:118440514	ATAAACCCCTGAAAC[-/AG]TGTGTTTATCAGTAA	4297
rs759685702	snp	C/T			upstream-variant-2KB	KMT2A	GRCh38.p7	11:118435446	CGCTCTCCTCCTCCC[C/T]CTCTCTTAATCAGAA	4297
rs760142198	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118490892	TTCTTACAAATGTGT[A/G]AGAAACTTCTCTCTT	4297
rs760246118	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118450482	TTCTCTAGTTACAAA[A/G]TGAGTAGCATTTGTG	4297
rs760469192	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118465229	GTGACAGAGTGAAAC[G/T]CTTATCTTAAAAAGA	4297
rs760547801	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118469185	TCTTATCTATCAGGC[C/T]ACATTGGGTTTATTC	4297
rs760983904	snp	C/T	0.000263904	0.011484	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521438	TCTCCCACTTGCACT[C/T]ACACAGTTCTTTTGT	4297
rs761064369	snp	A/G			synonymous-codon	KMT2A	GRCh38.p7	11:118480198	ATGTCAGAATCTACA[A/G]TGGATGCCTTCCAAA	4297
rs761377647	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118458623	CACACTCTAAAGAAG[A/G]CAAATGTGTGAACAC	4297
rs761393864	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118493759	CTGTTACCCAGGCTG[G/T]CATGCAGTGACATGA	4297
rs761787498	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118475422	ATGGCCATAAACTTA[C/T]ATTTGTAATGTTATT	4297
rs762073230	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118443818	CCAGTGGGCAGCATC[A/G]GTCCAGTAGCATTTA	4297
rs762335703	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118485029	AAATTATTTTTCTGT[A/G]GATGAAATTACTATA	4297
rs762361864	snp	A/G			upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118525810	TTTTGTTTTTAAGGA[A/G]AAGCGGGTCATTGCA	4297
rs762536601	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118459779	CCCAACCCCCCGCCC[C/T]GGGTTCAAGCAATTC	4297
rs762926042	snp	C/T			upstream-variant-2KB	KMT2A	GRCh38.p7	11:118435191	TCCCCCAGCCTCAGC[C/T]AACGCAAGTTCTCCC	4297
rs763186376	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118510864	AAGATTCTATTAAAG[A/G]AGAAAATGGAATTTG	4297
rs763494078	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118490469	TTATAACTAACCACA[A/G]AGAAATCCTCTAAGC	4297
rs763685802	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118488051	CAGGTGTGGTGGCAC[A/G]CGCCTGTGATCCCAG	4297
rs763776428	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118491041	AGAATAATCTTGAGA[C/T]TGCAGATGTGTGAAC	4297
rs764088480	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118469722	TAGACACTCCAGCTA[A/G]ATATGATATTGTTAG	4297
rs764147732	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118465455	TTAATTCCATTTTCC[A/G]TGAACCTTTTGAAGT	4297
rs764397442	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118497474	GCTTTTGGCTCACTG[C/T]AATCTCGGCTTCCGG	4297
rs764505268	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118437210	ATCCCTTGGCACAGA[C/T]CCCCTCGCCGGGGTT	4297
rs764539270	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118517952	TGCAGTGGCATGATC[A/G]TCTGCTTTTTCATCT	4297
rs764942352	snp	A/C	1.64741e-05	0.00286998	synonymous-codon	KMT2A	GRCh38.p7	11:118491266	GATGATGCAATGTGG[A/C]AAGTGTGATCGCTGG	4297
rs765697979	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118485074	TATTTAGCAGGTACT[-/A]TTCCCTGTTTAAACC	4297
rs765817466	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118487247	TTTTATAGCACCAGT[C/T]CTTCAACTTCTGGGA	4297
rs766330532	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118494268	TTTAAGAATAATTAA[C/T]ATTTTGTTTTTGTAT	4297
rs766489123	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118475987	CTTGGCTCACTGCAA[C/T]GTCCGCCTCCCAGGT	4297
rs766672797	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118507836	GGCGTGATGGCGGGC[A/G]CCTGTAGTCCCAGCC	4297
rs767267936	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118485604	ATTATTTGGAAATAT[A/G]TATCTATCTTTAAAA	4297
rs767281212	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118465193	CAGTGAGCCAAGATT[C/G]TGCCACTGCACTATA	4297
rs767466774	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118460738	CAGGTGCAATAATAG[A/G]GGACCACAGCCTTGA	4297
rs767997756	snp	C/T			intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118511831	ATAACAAAACACTGC[C/T]CTAGGAGGGCAAGTG	4297
rs768113799	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118493740	TTTGAGATGGAGTCT[C/T]GCTCTGTTACCCAGG	4297
rs768694882	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118509699	GAAAAACTATCAGAT[C/T]GTCATACTAGAAATT	4297
rs768785037	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118449090	TAAAAAATACCAGGG[A/G]CTTTCTTTTTTTTAA	4297
rs768838451	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118443613	GTTGAATTGAATGTA[C/T]TGCCCTAATGAGTTT	4297
rs768896167	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118489447	TAAGATTTTGTATCT[A/G]TATTATTTCTCTTTT	4297
rs769221157	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118464246	ATTCTGACTGAAAAA[C/G]TAAAGTTGGCTGGGC	4297
rs769365560	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118499541	GTAATCCCAGCACTT[A/T]GGGAGGCTGAGGCGG	4297
rs769576027	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118438304	GCAAGAACGGAGTTG[A/C]TTCTATAAACATTAT	4297
rs769824763	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118478510	GCGCTTGACATGTGA[C/T]TAGTGTGACTGAGGA	4297
rs770019077	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118452558	CTTTTTCCCTCCTGT[G/T]AAAATGGAACTTAGA	4297
rs770351051	in-del	-/AAGTA			intron-variant	KMT2A	GRCh38.p7	11:118490073	AAGATCTTTTTAGTT[-/AAGTA]AAGATATTAAAAACA	4297
rs770458074	snp	A/G	1.64787e-05	0.00287038	missense	KMT2A	GRCh38.p7	11:118505437	CACCAAACATCAGCA[A/G]TCCTCCTTCAGGCCT	4297
rs770459353	in-del	-/AAAT			upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118525970	TTTGTTTTGGTTTTC[-/AAAT]AAATATAAATATGAT	4297
rs770541345	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118464583	AGCAACTTTCTACCA[A/C]ATGGGTGCCAAAACC	4297
rs770640843	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118500114	TTATAGAAGGAAAGT[A/G]TTATTGACATAATTT	4297
rs770732347	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118439761	AGAAGAGTGGTTGAC[C/T]CCTTACATTAAACTT	4297
rs770806396	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118443349	GATGAGCCGCTTTTC[C/T]TGACCTATCCAAAGA	4297
rs771062659	snp	C/T	1.6585e-05	0.00287962	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519830	AGCAGTTTTGGGTCT[C/T]GATTTTCTTATCTCA	4297
rs771122086	snp	C/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118515635	TTAGGAACAAATGGA[C/T]ATCTCACAGACCAGA	4297
rs771280739	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118457660	AATTTCACTCCATGC[A/C]ACATTCTTTTGTGTC	4297
rs771532622	snp	C/G/T			synonymous-codon	KMT2A	GRCh38.p7	11:118493119	TTCCCGCAGCTCCCC[C/G/T]GAAGGACCTGATCCA	4297
rs771582258	snp	C/T	3.333e-05	0.00408214	synonymous-codon	KMT2A	GRCh38.p7	11:118474297	GAGTCTTAAACAAAC[C/T]GACCAGCCCAAAGCA	4297
rs771768830	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118468506	TATAGTTTGAAATTA[A/G]GACTATCCTCTGTGT	4297
rs771962002	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118447406	CATAAACTAGGAGAA[C/T]TTAAGACTACGAACA	4297
rs771969296	snp	C/T			missense	KMT2A	GRCh38.p7	11:118505989	TTCCAGGACACGTCA[C/T]CTTAACCAACCCAAG	4297
rs772195191	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118486606	CGTCGGGTGCAGTGG[C/T]TCACGCCTGTAATCC	4297
rs772304745	snp	G/T			utr-variant-3-prime, intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118524878	ACTGTGAGCCCCTCC[G/T]CACTCTCTACCAACC	4297
rs772587977	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118458307	AGAACTAGGCTGGTC[C/T]ACAACTCCTGGGCTC	4297
rs772645105	snp	C/G			missense	KMT2A	GRCh38.p7	11:118495885	ATCCTCCTACACCAC[C/G]AATTTTGAGTAAGCC	4297
rs772662209	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118464356	GCCTGGCCAACATGA[C/G]GAAACCCCATCTCCA	4297
rs772717209	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118459568	ATTGGAGCTTATTCA[A/G]TAGAGGAATTCTCAA	4297
rs772910633	in-del	-/CT			intron-variant	KMT2A	GRCh38.p7	11:118496117	GATGAGGTAGCGTAA[-/CT]CTGAACACTTTTTGA	4297
rs773084602	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118438523	GTAGGGGGTTGCTGC[C/T]CTGGAGTGCTCTTGA	4297
rs773347246	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118452691	CAGGCTGGAGTGCAG[C/T]GGCGCCATCTCGGCT	4297
rs774211376	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118496556	TTTGTCACTTAGTTC[A/G]TGGCACTTGGAGTTT	4297
rs774365740	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118482720	TTCAAGACCAGCCTG[A/G]GCAACATAGCAAGAC	4297
rs774384850	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118440313	GTAGAATTGAGGTTT[G/T]GTTTTATTGAGCACT	4297
rs774415018	snp	C/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520667	AAAAAAAAAGGGGGG[C/T]GCTCATTTTATAAGG	4297
rs774610839	in-del	-/TAC			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118515966	CGCTGAGAGTACAGG[-/TAC]TACCCAGCCCCATGT	4297
rs774992425	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118453635	TGACTACTTCTCAGA[A/G]TTCCAGGCTTGTATA	4297
rs775025829	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118490762	GTTATACAGAGTACT[C/G]AATCTTAGGAAGTGC	4297
rs775095951	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118468624	ATTTATTTCAATATT[A/C]GTTATTTTATAGTAT	4297
rs775486061	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118443520	TTACGTGATTTGTAA[C/T]TGTTGTGGATGATAT	4297
rs775730474	snp	C/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118516707	TGTGCTGTAAATATT[C/T]ATTGAATGAATAAAT	4297
rs775733457	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118483950	GAGGCAGGAGGATCA[C/T]GAGCCCACAAGGTCT	4297
rs775883126	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521141	GCCATGTGTTAGATG[A/G]CCAAATCAAGTGGGT	4297
rs776154752	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118454738	CCATTAACAACTGAA[C/T]GTGGCCATGTTCCAA	4297
rs776716231	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118449124	GTTAATGCCACCTAA[C/T]GTGGGCTTCTCAGAA	4297
rs776755606	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118469883	TGGTATTGTCATTCT[A/C]GTTGGGGGCAGTTGG	4297
rs776770204	snp	C/T	1.64947e-05	0.00287177	synonymous-codon	KMT2A	GRCh38.p7	11:118510000	CTCCCCACTGATGCT[C/T]TGGCTTCAGCAAGAA	4297
rs776771451	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118489473	CTTTTTACTTAGTCT[C/G]TCTTTAGCATTTAAT	4297
rs777018567	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118487083	CTTAGTCCCTATTAC[A/G]AACAACTTATTGTTC	4297
rs777072851	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521742	GAAATCCTCGTGGAA[A/G]CATCTTGAAAGATAG	4297
rs777149030	snp	C/T			upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118525528	TGCCGGGACCCAGCC[C/T]GCCACCCTGCTCGCC	4297
rs777598668	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118442255	GGAAGCTTTGTGACT[A/G]TCACTACTTTGGGAG	4297
rs777759428	snp	A/T			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118523013	GTGCCTGCAAAAAGT[A/T]CCCTGAGCCTGTAAG	4297
rs778180072	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118495151	CTTTTGATTTGATTT[G/T]ATTTATTTATTTATT	4297
rs778424780	snp	C/T			intron-variant, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512081	TTATGGTAAATTGTT[C/T]GCCTAAGGCAGAGTT	4297
rs778426115	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118508888	AAGAATTTCAAGGGC[A/G]CAATTTACAACTTTA	4297
rs778675942	snp	C/T			missense	KMT2A	GRCh38.p7	11:118505574	AAAAGACCCATATCT[C/T]GTCTACAGACCCGAA	4297
rs778700222	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118443370	TATCCAAAGAAATCC[A/G]TACCACCACTGTTAA	4297
rs778858979	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118486598	AAAATCCACGTCGGG[C/T]GCAGTGGCTCACGCC	4297
rs778914461	snp	A/G			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118523537	ATTTTACTCTGTTCT[A/G]TTTACAGTTTACTAT	4297
rs779361151	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118457835	TCTTTCTGCTGTGCT[C/T]CTCCAGCAGTGTCTT	4297
rs779561229	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118481174	GTTGTACTATCAAAT[-/A]CTAGATCTCATTCAC	4297
rs780010419	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118448066	TCCTCGAAGCAATAA[C/T]TACTTTCCAGTAGGA	4297
rs780538462	snp	C/T	1.64749e-05	0.00287005	synonymous-codon	KMT2A	GRCh38.p7	11:118502945	GAATGTTAGTAAAAT[C/T]GGCTCCTTTGCTGAA	4297
rs780609278	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118463889	TTGAGGCACTAAGAA[A/G]GATAAGACATCAGTT	4297
rs780783879	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118442007	TGCTTGCTCAGAGGC[A/C]TAACAGACTGCAGTG	4297
rs780980336	in-del	-/GGG			intron-variant	KMT2A	GRCh38.p7	11:118437918	GGGGAGGTGTTTGTT[-/GGG]GGACTGAGGCAGCAT	4297
rs781023500	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118456766	ATTCATATATTCATT[A/G]AGTCAGATGTGTTTT	4297
rs781782812	snp	A/G	8.34982e-05	0.00646082	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520759	AAGACTCAAAACATT[A/G]TTTCCTGAAAAAAAT	4297
rs781784128	snp	G/T	1.64735e-05	0.00286993	missense	KMT2A	GRCh38.p7	11:118505059	CCAATTCTACTGATA[G/T]TCCTGGCCCGTCTCA	4297
rs781784357	snp	C/T	4.97723e-05	0.00498835	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473688	GTTTACCCCAGGCTC[C/T]CAGACTGAAAGAGGG	4297
rs781784530	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118515578	GCAGCAGTTCCCACA[A/G]TAACATTCAGTCATC	4297
rs781785518	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118454100	ACCTCAGACTCTCCC[A/G]TTATAGTCTCTTGGT	4297
rs781786089	snp	A/G	1.65198e-05	0.00287395	missense, intron-variant	KMT2A	GRCh38.p7	11:118473114	TATTTGATAATTTCC[A/G]ACCCCCTCCACTAAC	4297
rs781786930	snp	A/T	1.64798e-05	0.00287047	missense	KMT2A	GRCh38.p7	11:118503523	AAAATGCCCTGAAAG[A/T]AAGTAGTCCTGCTTC	4297
rs781787241	snp	A/G	9.88419e-05	0.00702931	missense	KMT2A	GRCh38.p7	11:118493120	TCCCGCAGCTCCCCC[A/G]AAGGACCTGATCCAC	4297
rs781787305	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118498815	AATGTATAATGATGT[A/G]TATCCACCATTATAC	4297
rs781788502	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118466741	AATCTCTTGAACCTG[C/G]GAGGCTGAGGTGGCG	4297
rs781788826	snp	C/T			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522487	ATAGAGGGTTGGTTA[C/T]GTTGGGAGATTGGGC	4297
rs781789464	snp	A/G	4.94458e-05	0.00497197	synonymous-codon	KMT2A	GRCh38.p7	11:118484197	GGAAAAACCACCTCC[A/G]GTCAATAAGCAGGAG	4297
rs781789564	snp	C/T	1.65422e-05	0.0028759	synonymous-codon	KMT2A	GRCh38.p7	11:118504136	TCCAAAAAGAAATGG[C/T]AAAGAAAATGGAACA	4297
rs781789646	snp	A/G	1.65507e-05	0.00287664	missense, intron-variant	KMT2A	GRCh38.p7	11:118472631	CCTCCACAGACTCTC[A/G]GGCTTCTGAGGAGAT	4297
rs781790351	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118510662	TATCACTCACTCAAC[A/T]GCGAGCTCTCCATAA	4297
rs781790615	snp	C/T	5.20775e-05	0.00510255	intron-variant	KMT2A	GRCh38.p7	11:118474327	ACAGGTACTCTTTTC[C/T]ACCTTGCCTATTAAA	4297
rs781790977	snp	A/T	6.60895e-05	0.00574808	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519806	AGGCAAGTTCCCTTC[A/T]TTTCTGTCAGCAGTT	4297
rs781792393	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118446274	GAATCGCTTGAACCC[A/G]GGAGGCAGAGGTTGC	4297
rs781793118	snp	C/T	1.71507e-05	0.00292832	intron-variant	KMT2A	GRCh38.p7	11:118494688	TTTGTTTGTGTTTTC[C/T]TTTAGCAAATGGAAC	4297
rs781793404	snp	C/G	1.65127e-05	0.00287334	missense	KMT2A	GRCh38.p7	11:118503252	TTTTTGGAACCTGGT[C/G]AGGTGACAACTGGTG	4297
rs781793601	in-del	-/TCGTCT	4.49913e-05	0.00474275	cds-indel	KMT2A	GRCh38.p7	11:118436779	TCCTCGTCGTCCGCC[-/TCGTCT]TCGTCTTCGTCTTCG	4297
rs781793777	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118517911	TGTTTTTGAGATGAG[A/G]TCTCACTCTGTTGCC	4297
rs781794132	snp	A/T	1.67815e-05	0.00289663	missense, intron-variant	KMT2A	GRCh38.p7	11:118471710	CTAGAAGTGGCTCTG[A/T]CCGAAATTCAGCTAT	4297
rs781794901	snp	C/T	1.64991e-05	0.00287215	intron-variant	KMT2A	GRCh38.p7	11:118468763	TTTTAAAATAATTTT[C/T]CTTTGTTGTAGGATG	4297
rs781795624	snp	A/G	1.6492e-05	0.00287154	missense	KMT2A	GRCh38.p7	11:118499849	GGGTCTATGACAATC[A/G]ACTGCTTAGGAATTC	4297
rs781795821	snp	C/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512298	TCATTAGCAGTCATT[C/T]CTCAGCCCCTGGCCA	4297
rs781796447	in-del	-/G	1.65655e-05	0.00287793	intron-variant	KMT2A	GRCh38.p7	11:118468740	TGTATGCACGTTTTT[-/G]CTTCTGATTTTAAAA	4297
rs781796481	snp	C/G	1.64939e-05	0.0028717	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473475	CTCACCTCTCACCCC[C/G]CCGTCTTCTGTCTCT	4297
rs781796607	snp	C/T	1.64765e-05	0.00287019	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118472873	ACTCCACCGCCACCA[C/T]TGCAGCCAGCCTCCA	4297
rs781796692	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118452580	GAACTTAGATGTGAC[C/T]ACATGCTCTGCTGCC	4297
rs781797424	snp	C/G	1.64808e-05	0.00287057	missense	KMT2A	GRCh38.p7	11:118476833	ACTCATCAGAGACCT[C/G]TGTGCGAGGACCCCG	4297
rs781797746	snp	A/C/G	3.29768e-05	0.00406048	missense, synonymous-codon	KMT2A	GRCh38.p7	11:118510048	CATTACTGAGAAAAA[A/C/G]CCCAAGAAAGGACTT	4297
rs781797864	snp	A/C	1.65187e-05	0.00287386	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118472417	AGTGCTATCTCCTCG[A/C]GGATCATTAAGACCC	4297
rs781798054	snp	C/T	2.03147e-05	0.00318699	missense	KMT2A	GRCh38.p7	11:118436700	CGGCTGTGGCGGCCG[C/T]GGCGGCGGCGGCGGG	4297
rs781798126	snp	C/T	5.23218e-05	0.0051145	synonymous-codon	KMT2A	GRCh38.p7	11:118436722	GGCGGCGGGAAGCAG[C/T]GGGGCTGGGGTTCCA	4297
rs781798587	snp	A/C	1.64795e-05	0.00287045	missense, intron-variant	KMT2A	GRCh38.p7	11:118474029	ATACAACAGCTGTCA[A/C]AACCAAAATACTTAT	4297
rs781798961	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118450615	CAGAGAATTATTGTC[C/T]TAGCGCTCTTTAATC	4297
rs781799317	snp	A/T	1.65312e-05	0.00287495	missense	KMT2A	GRCh38.p7	11:118507555	CAGAGGCTGAGCAGC[A/T]GGATACAGCTAGCGT	4297
rs781800324	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118507008	TTTTTAAAACTTTAT[C/T]ATTGAAAGCCAAGCA	4297
rs781800986	snp	A/G	1.64963e-05	0.00287192	synonymous-codon	KMT2A	GRCh38.p7	11:118501014	ATACTGGAGCACCAC[A/G]GATGCTCGCAAGCGC	4297
rs781801231	snp	C/T	1.6477e-05	0.00287024	synonymous-codon, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522125	GATGCCAGCAACAAG[C/T]TGCCCTGCAACTGTG	4297
rs781801270	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118458666	TCCTTCTGCTAATAC[G/T]AGTAATTATGTGAGC	4297
rs781801551	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118444860	GATTACAAATGTGAG[A/G]CACTGCACCCAACCA	4297
rs781802334	snp	A/T	3.5823e-05	0.00423205	splice-acceptor-variant	KMT2A	GRCh38.p7	11:118502396	TTTTCTCTCTTGTTT[A/T]GGAAGTCCTACCCCA	4297
rs781803942	snp	C/G	1.68724e-05	0.00290446	missense	KMT2A	GRCh38.p7	11:118506601	CCAGTTCTTCTGAAG[C/G]ACACATTCCAGACCA	4297
rs781804121	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118488557	GAAGGGTATGGTTGA[C/T]TATGTTTTTCTACAT	4297
rs781804532	snp	C/G	1.64874e-05	0.00287113	missense	KMT2A	GRCh38.p7	11:118506145	GGACATCACAGACCC[C/G]CTCTACTGCTGCAAT	4297
rs781805197	snp	A/G	1.64727e-05	0.00286986	missense	KMT2A	GRCh38.p7	11:118478068	CCCCAGGAACCTCCA[A/G]TAAAGAAAGGACGTC	4297
rs781805421	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118481301	TCTCTATCTCCATAA[A/G]TTCAATTGTTTTAAT	4297
rs781805479	snp	C/T	3.30486e-05	0.00406487	missense	KMT2A	GRCh38.p7	11:118495819	TGAAGAAAATCATTC[C/T]AGCTCCCAAACCCAA	4297
rs781805661	snp	C/G	0.000183033	0.00956467	missense	KMT2A	GRCh38.p7	11:118498526	GATTTGATCAAAGGC[C/G]AAGTGAGAGAGCTTT	4297
rs781805862	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118440299	ATGACAATTAGGAAG[C/T]AGAATTGAGGTTTTG	4297
rs781806682	snp	C/T	1.64735e-05	0.00286993	missense, intron-variant	KMT2A	GRCh38.p7	11:118473875	AGTAGTTCTGCTTTG[C/T]ATCCTGTGGGTAGGG	4297
rs781806860	snp	A/G	3.30033e-05	0.00406209	missense, intron-variant	KMT2A	GRCh38.p7	11:118473389	AAAGTGTTTAGTCCT[A/G]TTCGATCTGAACCAA	4297
rs781807137	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118447301	TTTATGTTTTATGTT[C/T]TTTATAATGGTGACT	4297
rs781807340	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118495025	CATGTGTGGTACAGC[C/T]ATGTAGCTGGCCTTG	4297
rs781807704	in-del	-/A	4.99704e-05	0.00499827	intron-variant	KMT2A	GRCh38.p7	11:118489777	TATCTTTTTGCCATT[-/A]ATATTTTCTTACAGC	4297
rs781808874	snp	A/G	5.01308e-05	0.00500628	intron-variant	KMT2A	GRCh38.p7	11:118482536	ATTTCTCAGGGATGT[A/G]TTCTATTTTGTAGGG	4297
rs781809083	snp	A/G	1.64762e-05	0.00287016	synonymous-codon	KMT2A	GRCh38.p7	11:118506494	AAGCCCTTCAGTGCC[A/G]GGTCCCACTAAACCC	4297
rs781809969	snp	C/T	0.000148269	0.00860886	missense	KMT2A	GRCh38.p7	11:118503679	ATCAGAATCTTCCAG[C/T]ACAGGACAGAAACCT	4297
rs781811920	snp	A/G	4.97244e-05	0.00498596	intron-variant	KMT2A	GRCh38.p7	11:118499468	GTATATATCATTGGG[A/G]AAATTTCTGGTCCTC	4297
rs781812638	snp	A/T	1.64819e-05	0.00287066	missense	KMT2A	GRCh38.p7	11:118506010	CCAACCCAAGGTTGC[A/T]TGGTACCCCAGATAT	4297
rs781812939	snp	G/T	2.90221e-05	0.00380923	intron-variant, missense	KMT2A	GRCh38.p7	11:118439095	GACTGAACCGTTCAG[G/T]TTACTTGCATGGAGT	4297
rs781814523	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118455528	TGACCATACCATACA[A/G]GAATTAACAAGGTTC	4297
rs781815053	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118491027	TATTCGAGGGGCTCA[A/G]AATAATCTTGAGACT	4297
rs781816490	snp	C/T	1.66186e-05	0.00288254	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118471912	GGGAAACAAAGAAGA[C/T]AGCCTGAAAAAAATT	4297
rs781816491	snp	A/G	1.64863e-05	0.00287104	missense	KMT2A	GRCh38.p7	11:118489850	AGTGCCTGGGACCAA[A/G]CTACCCCACCAAACC	4297
rs781816513	snp	C/T	1.65151e-05	0.00287355	missense	KMT2A	GRCh38.p7	11:118504174	TAAAGATTGATAGAC[C/T]TGAAGATGCTGGGGA	4297
rs781816624	snp	C/G	3.32945e-05	0.00407997	missense	KMT2A	GRCh38.p7	11:118509163	TCTTCCGGAAGTTCA[C/G]GTGACCCAAAATCCA	4297
rs781817780	snp	A/G	1.648e-05	0.0028705	missense	KMT2A	GRCh38.p7	11:118504868	TCCTGAAGGCCACAT[A/G]ACTCCTGATCATTTT	4297
rs781818062	snp	A/G	1.65203e-05	0.002874	missense	KMT2A	GRCh38.p7	11:118502694	ACTTCCACCTCTTCA[A/G]ATTTGCAAAGGACAG	4297
rs781818465	snp	A/G	1.64904e-05	0.00287139	missense	KMT2A	GRCh38.p7	11:118480175	CGTTGTTTTCCTAGG[A/G]TGAGAAAATGTCAGA	4297
rs781818869	snp	A/C/G	3.30225e-05	0.0040633	missense, intron-variant	KMT2A	GRCh38.p7	11:118472727	CCCCAGAAAATGAGA[A/C/G]TAATGATAGGAGAAG	4297
rs781819293	snp	C/G	0.000148279	0.00860914	missense	KMT2A	GRCh38.p7	11:118503345	CGACCATGTAACAAT[C/G]TTTCTTCTGATAAGA	4297
rs781819920	snp	C/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521512	AAATAGTGTATGTTA[C/T]CAATTCAGAGACCTT	4297
rs781821970	snp	A/G	1.64944e-05	0.00287175	missense	KMT2A	GRCh38.p7	11:118504063	AGTTGGATGGTGTTG[A/G]TGATGGGACAGAGAG	4297
rs781822024	snp	A/G	1.65337e-05	0.00287517	intron-variant	KMT2A	GRCh38.p7	11:118484319	TGGACTTTAAGGTAA[A/G]GGTGTTCAGTGATCA	4297
rs781822139	snp	C/T	1.64779e-05	0.00287031	synonymous-codon	KMT2A	GRCh38.p7	11:118504562	TCTTGACAGTAATCG[C/T]GAAAAAGACATGGGT	4297
rs781822315	snp	C/T	0.000198079	0.00994988	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118434630	TCCACAATGGGGTGT[C/T]TCTGTCCTTAGCAGA	4297
rs781822608	snp	G/T	1.64741e-05	0.00286998	missense, nc-transcript-variant, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519662	CTCCATGATGCAGTT[G/T]TGTTCCTCATTGAGC	4297
rs781822906	snp	A/T	1.64974e-05	0.00287201	missense	KMT2A	GRCh38.p7	11:118474218	AGCTTCCAATGACTG[A/T]CAAGAGGGTTGCCAG	4297
rs781823487	snp	A/C	1.65466e-05	0.00287628	missense	KMT2A	GRCh38.p7	11:118481979	GCAAGCAGGTCTCCC[A/C]GCCAGCACTGGTCAT	4297
rs781823685	snp	A/C	2.22883e-05	0.00333821	synonymous-codon	KMT2A	GRCh38.p7	11:118436806	TTCGTCATCGTCCTC[A/C]GCCTCTTCAGGGCCG	4297
rs781823826	snp	C/G/T	3.5027e-05	0.0041848	missense	KMT2A	GRCh38.p7	11:118491918	CCAGCCATTTGCTAC[C/G/T]CTACCGGCAGGTAGG	4297
rs781824294	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521813	TCAGCCGCTATAGGT[A/G]ACATCAAGAGAAGAT	4297
rs781824886	snp	A/G	1.64849e-05	0.00287092	missense	KMT2A	GRCh38.p7	11:118505241	AGTTCTACACCCAGT[A/G]TGATGGAGACAAATA	4297
rs781825703	snp	C/T	4.94678e-05	0.00497307	synonymous-codon	KMT2A	GRCh38.p7	11:118502876	ACATAATGTGGCTTA[C/T]CCTGGAATTCCTAAA	4297
rs781826148	snp	A/C			missense	KMT2A	GRCh38.p7	11:118499873	GGAATTCTAAATGAT[A/C]TCTCCGACTGTGAAG	4297
rs781827264	snp	A/G	1.64741e-05	0.00286998	intron-variant	KMT2A	GRCh38.p7	11:118509919	TGAGCATTTGTTACT[A/G]CAACCACTATCTATT	4297
rs781828113	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118486203	ATGGAAAGATGTCCA[C/T]GACATATCACTGAGT	4297
rs781828974	snp	G/T	1.96868e-05	0.00313736	intron-variant	KMT2A	GRCh38.p7	11:118482131	ATTGCTGAACCACAA[G/T]TACTAACAAAAAAGC	4297
rs781829726	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118463075	TAAAAATGACTCATT[A/G]GGTTGTTAATAATGA	4297
rs781829749	snp	C/T	3.44364e-05	0.00414934	synonymous-codon	KMT2A	GRCh38.p7	11:118490227	CTCACTGTGTCATGA[C/T]TGCGCCAAGCTCTTT	4297
rs781830267	snp	A/G	8.23757e-05	0.00641725	missense	KMT2A	GRCh38.p7	11:118503696	CAGGACAGAAACCTA[A/G]TGCTTCCAGATGGCC	4297
rs781830772	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118460329	GGACTTGCTCTGTCA[C/T]CCAGGCTGGAGTGCA	4297
rs781831426	in-del	-/AGTGGACTTTAAGGTAAAGGTGTTCAGTGATCAT	3.30126e-05	0.00406266	frameshift-variant	KMT2A	GRCh38.p7	11:118484301	AGTCCACAGGATCAG[lengthTooLong]AGTGGACTTTAAGGT	4297
rs781831865	snp	C/T	1.77896e-05	0.00298237	intron-variant	KMT2A	GRCh38.p7	11:118507659	CTCAGTTTTGTCCAC[C/T]TCATTTAAAAAATAG	4297
rs781831913	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118466382	GGCTAGCCTTGAACT[C/T]CTGGCCTCAAGCAGT	4297
rs781832439	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118510547	CAGACGGTCTTCCCT[A/G]ACCTTCTGAGGTAGC	4297
rs781832472	in-del	-/T			intron-variant	KMT2A	GRCh38.p7	11:118476711	TGTTTTGATTCTAAA[-/T]TCATACTGAAATTGA	4297
rs781832858	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118500326	ATCAAATTTTTCAAT[A/G]AGAATTTATAATCTT	4297
rs781832980	snp	A/C	1.7221e-05	0.00293432	intron-variant	KMT2A	GRCh38.p7	11:118495927	AGTCGTCACCCATTT[A/C]CCTCTAGATGCAGAT	4297
rs781835065	in-del	-/TTT	1.76235e-05	0.0029684	intron-variant	KMT2A	GRCh38.p7	11:118498568	AAAAAAAAAAAAGAC[-/TTT]TTTTTTAGAGCAGTT	4297
rs781835226	snp	A/G	3.29728e-05	0.00406021	intron-variant	KMT2A	GRCh38.p7	11:118488571	ATTATGTTTTTCTAC[A/G]TATTATTTGACATAC	4297
rs781835391	snp	C/G	3.32552e-05	0.00407756	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473703	TCAGACTGAAAGAGG[C/G]AGAAATAAAGACAAG	4297
rs781835429	in-del	-/A/AA	0.0341001	0.126163	intron-variant	KMT2A	GRCh38.p7	11:118498550	AGCTTTAGTTGCTTT[-/A/AA]AAAAAAAAAAAAAAA	4297
rs781835522	snp	C/G	1.64735e-05	0.00286993	missense	KMT2A	GRCh38.p7	11:118493180	GATCAGCAGCCTTTA[C/G]ATCTAGAAGGAGTCA	4297
rs781835973	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118516936	ATTGTAATCTCTCTG[A/G]TGAGTGAGAGTTGAA	4297
rs781836381	in-del	-/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118515979	AGGTACCCAGCCCCA[-/T]GTCCATTTCTAAGCC	4297
rs781837466	snp	C/T	3.30387e-05	0.00406427	missense, intron-variant	KMT2A	GRCh38.p7	11:118472465	GATGAGGATTATGAC[C/T]CTCCAATTAAAATTG	4297
rs781838224	snp	A/G	1.73978e-05	0.00294934	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520936	GAATGCAGTTTTTCA[A/G]AATCAAAGCAGACCA	4297
rs781838580	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118475363	TTAAAAAAATCGTCA[C/T]GTAGTAGATGCCTAT	4297
rs781838646	snp	A/T	1.64738e-05	0.00286995	synonymous-codon	KMT2A	GRCh38.p7	11:118506368	CCAGACGGTAGACGC[A/T]CCTAATAGCATGGGA	4297
rs781840426	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118441918	TTAGAGCTGTCCTTC[C/T]GTGGGGCAGCTGTGC	4297
rs781840795	snp	C/G			missense, intron-variant	KMT2A	GRCh38.p7	11:118472132	ATTAATTCTGAACTG[C/G]AAAAGCCCCAGAAAG	4297
rs781841326	snp	C/T	1.64746e-05	0.00287002	synonymous-codon	KMT2A	GRCh38.p7	11:118499380	CTTGAGAAGGAAGTT[C/T]CTCAATGGCTTGGAA	4297
rs781842495	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118456143	ACCTGGCCTCTCCCT[A/G]TTACTGTTAATCAGC	4297
rs781842820	snp	C/T	3.29946e-05	0.00406155	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473487	CCCCCCGTCTTCTGT[C/T]TCTTCCTCGTTAAGC	4297
rs781843315	snp	C/G	3.2956e-05	0.00405918	missense	KMT2A	GRCh38.p7	11:118501797	AAGGTCCCCAGGATT[C/G]GAACACCCAGTTATT	4297
rs781843828	snp	G/T	1.6546e-05	0.00287624	intron-variant	KMT2A	GRCh38.p7	11:118496414	ATACATACTCCAAAA[G/T]AACTGTTTGTCCTTG	4297
rs781846454	snp	A/G	3.29495e-05	0.00405877	missense, intron-variant	KMT2A	GRCh38.p7	11:118472897	GCCTCCAGTATCTCT[A/G]ACCACACACCTTGGC	4297
rs781846955	snp	C/G	0.000181227	0.00951738	missense	KMT2A	GRCh38.p7	11:118506252	GCAGACGAACACTAT[C/G]AGCTTCAGCATGTGA	4297
rs781847193	snp	A/G	6.80654e-05	0.00583336	intron-variant	KMT2A	GRCh38.p7	11:118494783	GTAAGTGAATTTAGC[A/G]TAACTTTTTTTTCTC	4297
rs781847861	snp	G/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519892	GATTTCCAGTTTTAA[G/T]GCCATCATCCTTTAC	4297
rs781848142	snp	A/G	3.29794e-05	0.00406061	missense	KMT2A	GRCh38.p7	11:118499879	CTAAATGATCTCTCC[A/G]ACTGTGAAGATAAGC	4297
rs781848545	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118439726	ACTTTTTCCTGAACA[A/G]TAGTTGCTGCTTCAT	4297
rs781848874	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118496757	AGCCCGAGTTCTGCC[A/G]CCTGCCTGAATACAT	4297
rs781850395	snp	C/T	9.77756e-05	0.0069913	missense	KMT2A	GRCh38.p7	11:118436709	CGGCCGCGGCGGCGG[C/T]GGCGGGAAGCAGCGG	4297
rs781850427	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118475681	TGAGCCGAGATCACG[A/G]CACTACACTCCAGCC	4297
rs781850447	snp	A/G	1.65157e-05	0.0028736	intron-variant	KMT2A	GRCh38.p7	11:118498100	TGGGTAAATTTTATG[A/G]AAGAGATTCCCTCTC	4297
rs781850448	snp	A/G	3.29457e-05	0.00405854	missense	KMT2A	GRCh38.p7	11:118505931	TCTGTCTTGAATGTT[A/G]TATCCATGCAAACTA	4297
rs781850643	snp	A/G	3.63498e-05	0.00426305	intron-variant	KMT2A	GRCh38.p7	11:118482099	CAGAATCAGGTGAGT[A/G]AGGAGGGCAAGAAGG	4297
rs781850824	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118446209	CAATAATTAGCTACA[A/T]GTCGTGGTGCACACC	4297
rs781851230	snp	A/G	1.64963e-05	0.00287192	synonymous-codon	KMT2A	GRCh38.p7	11:118501035	TCGCAAGCGCTGTGT[A/G]TATACATGCAAGATA	4297
rs781851252	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118444572	TTGAAAAAGTTTTTT[G/T]TGTGTTTTGTTTGGT	4297
rs781851366	snp	A/G	1.6501e-05	0.00287232	missense	KMT2A	GRCh38.p7	11:118502851	GTTCCAAGAGCTCAG[A/G]GGGATCTGCACATAA	4297
rs781851809	snp	C/G	0.000399381	0.0141255	synonymous-codon	KMT2A	GRCh38.p7	11:118506584	AGTTTCCCATTTGCG[C/G]ACCAGTTCTTCTGAA	4297
rs781852468	snp	C/G	1.64735e-05	0.00286993	missense	KMT2A	GRCh38.p7	11:118505794	TCATGTATTTTGAAC[C/G]GGCACCCCTGTTACC	4297
rs781852744	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118488191	TCAAAAAAATAAATA[A/G]ATAAAAATTAAAACA	4297
rs781852802	snp	C/T	9.95718e-05	0.00705521	intron-variant	KMT2A	GRCh38.p7	11:118468733	ATGTGTTTGTATGCA[C/T]GTTTTTGCTTCTGAT	4297
rs781853027	snp	A/G	1.64933e-05	0.00287165	missense	KMT2A	GRCh38.p7	11:118505276	AGTATTGGGACCCAT[A/G]GGAGGTGGTCTCACC	4297
rs781854914	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118498330	ACGTCTTAAAACATA[C/T]GAAAGTCTGAATAGG	4297
rs781855910	snp	A/C/T	1.73972e-05	0.00294929	missense	KMT2A	GRCh38.p7	11:118502413	GAAGTCCTACCCCAA[A/C/T]CACTCATGAAATAGT	4297
rs781857470	snp	A/G	1.80383e-05	0.00300314	intron-variant	KMT2A	GRCh38.p7	11:118474347	TGCCTATTAAAACTA[A/G]CAGTTTATTGAGCCC	4297
rs781857541	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118493387	AATGTATGAGTTATT[G/T]TAGCTTTGTGTTTCA	4297
rs781857853	snp	A/G	0.000132087	0.00812565	intron-variant	KMT2A	GRCh38.p7	11:118484160	GTGTGATTTTGTTCT[A/G]TATTCATCTTTTGTC	4297
rs781858437	snp	A/C/G	6.59439e-05	0.0057418	missense	KMT2A	GRCh38.p7	11:118504345	TCCACACAAGTACCC[A/C/G]CTCCGACAAAAATTT	4297
rs781858602	snp	A/G	0.000186341	0.00965069	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118435081	CAGTGCGCTGTACCG[A/G]TGCGGGAGTCCAGGA	4297
rs781859703	snp	C/T	3.29473e-05	0.00405864	missense	KMT2A	GRCh38.p7	11:118505070	GATAGTCCTGGCCCG[C/T]CTCAGATTTCCAATG	4297
rs781859799	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118484102	CTATTAATAAAATTT[G/T]TCATTTGCATTATTA	4297
rs781860369	snp	A/G	1.65184e-05	0.00287384	missense	KMT2A	GRCh38.p7	11:118481849	CCTGCCCCAAAGAAA[A/G]GCAGTAGTGAGCCTC	4297
rs781860916	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118490784	AGGAAGTGCTCCTCT[A/C]AGCTCTAATGTAAAT	4297
rs781862085	snp	A/G	1.64909e-05	0.00287144	synonymous-codon	KMT2A	GRCh38.p7	11:118506131	GTTTCCACAACTGGG[A/G]ACATCACAGACCCCC	4297
rs781862311	snp	C/G	1.64757e-05	0.00287012	missense	KMT2A	GRCh38.p7	11:118502970	GCTGAACCCTCTTCA[C/G]TGTCGTTTTCTTCTA	4297
rs781862712	snp	A/T			synonymous-codon	KMT2A	GRCh38.p7	11:118503533	GAAAGAAAGTAGTCC[A/T]GCTTCCCCTTTGCAA	4297
rs781862991	snp	A/G	1.65828e-05	0.00287943	synonymous-codon	KMT2A	GRCh38.p7	11:118481998	AGCACTGGTCATCCC[A/G]CCTCAGCCACCTACT	4297
rs781863004	snp	A/T	1.64781e-05	0.00287033	missense	KMT2A	GRCh38.p7	11:118503549	GCTTCCCCTTTGCAA[A/T]TAGAGTCAACATCTC	4297
rs781863312	snp	A/G	1.65002e-05	0.00287225	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473079	AAAGTATGCCAAAGA[A/G]GGTCTTATTCGCAAA	4297
rs781864198	snp	C/G	1.64743e-05	0.00287	missense, intron-variant	KMT2A	GRCh38.p7	11:118473888	TGTATCCTGTGGGTA[C/G]GGTTTCCAAAGAGAA	4297
rs781864279	snp	C/T	3.29478e-05	0.00405867	missense	KMT2A	GRCh38.p7	11:118505554	CTCCATCCTCTGGAC[C/T]CAAGAAAAGACCCAT	4297
rs781864733	snp	C/T			synonymous-codon, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521312	CCATGGCCGGGGTCT[C/T]TTCTGTAAGAGAAAC	4297
rs781865040	snp	A/T	6.60993e-05	0.0057485	missense	KMT2A	GRCh38.p7	11:118503132	GGAATGAGCAACAGA[A/T]CATCCATTATCAACG	4297
rs781866544	snp	C/T	1.65488e-05	0.00287647	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118472614	TAGCCCCAGTGTTGA[C/T]ACCTCCACAGACTCT	4297
rs781866935	snp	A/G/T	4.94583e-05	0.00497264	missense, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522143	CCCTGCAACTGTGGC[A/G/T]CCAAGAAATGCCGGA	4297
rs781867236	snp	A/G	1.66355e-05	0.002884	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520772	TTATTTCCTGAAAAA[A/G]ATTCGTTAATAGTAT	4297
rs781867752	snp	C/T	3.30486e-05	0.00406487	synonymous-codon	KMT2A	GRCh38.p7	11:118504166	AGAGAACTTAAAGAT[C/T]GATAGACCTGAAGAT	4297
rs781867843	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118476605	TTTTTATTTTTTGAT[G/T]AGAGGCCTTTTTTTG	4297
rs781868296	in-del	-/G	0.000118998	0.00771264	intron-variant	KMT2A	GRCh38.p7	11:118439170	AGCAAAAAAAAAAAA[-/G]AAAGAAAAAAAAGAA	4297
rs781868819	snp	A/G	3.29516e-05	0.00405891	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473844	AGAGAAAAGGAAAAA[A/G]GGATCAGAAATTCAG	4297
rs781869397	snp	C/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118515907	TGGCCAGGATGGTCT[C/T]GAACTTCTGACCTCA	4297
rs781870146	snp	A/G	3.332e-05	0.00408153	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118471933	GAAAAAAATTAAAAG[A/G]ACACCTTCTGCTACG	4297
rs781870373	snp	A/C/G	6.6264e-05	0.00575571	intron-variant	KMT2A	GRCh38.p7	11:118484327	AAGGTAAAGGTGTTC[A/C/G]GTGATCATAAAGTAT	4297
rs781871135	snp	A/C	1.65353e-05	0.00287531	missense, intron-variant	KMT2A	GRCh38.p7	11:118472358	AGGGAAGAAAGGTGA[A/C]GACACAGGTCAAAAA	4297
rs781871743	snp	G/T	1.64784e-05	0.00287035	missense	KMT2A	GRCh38.p7	11:118488706	GCTGGAAAATTGGTG[G/T]TGTCGTCGTTGCAAA	4297
rs781871965	snp	A/G	8.23866e-05	0.00641767	missense	KMT2A	GRCh38.p7	11:118503319	TTTTGACTCCTGAGT[A/G]TATGGGCCAACGACC	4297
rs781872314	snp	C/G	1.64789e-05	0.0028704	missense	KMT2A	GRCh38.p7	11:118504855	GAGTAGATCCAACTC[C/G]TGAAGGCCACATGAC	4297
rs781872417	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118510959	GCAGGACTGCATTTG[A/G]TGGGTTTAGAGTAGT	4297
rs781872445	snp	A/T	0.000185082	0.00961805	intron-variant	KMT2A	GRCh38.p7	11:118439150	TGCTTTTTTAAAAGA[A/T]ACAGCAGCAAAAAAA	4297
rs781872582	snp	A/G	0.000561877	0.0167518	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118434723	CGCGCTGTAACAACG[A/G]AATCTTGTTCTGTGT	4297
rs781872678	snp	A/G	2.59084e-05	0.0035991	intron-variant	KMT2A	GRCh38.p7	11:118494438	TTTTAATGCTTACCT[A/G]TAAGTAATTACCCTG	4297
rs781874357	snp	A/G	1.65425e-05	0.00287593	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473346	TGGAACATCTTCTTC[A/G]GGAGTATCCAATAGA	4297
rs781874908	snp	C/T			missense, intron-variant	KMT2A	GRCh38.p7	11:118473605	GAGAAAAATCAGAGA[C/T]CAAGGAAGCAGACTA	4297
rs781874946	snp	A/G			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522642	GGCCCCACCTACAGC[A/G]TCTGTCGAACAAACA	4297
rs781875512	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118478855	CTGAACTCCTAGGCT[C/T]CAGTGATCCTCCTGC	4297
rs781875933	snp	A/T	1.64735e-05	0.00286993	synonymous-codon	KMT2A	GRCh38.p7	11:118491808	TTGTGTGAACTGTAC[A/T]GAGCGGCACCCTGCA	4297
rs781876156	snp	A/G	0.000161188	0.00897597	missense	KMT2A	GRCh38.p7	11:118436816	TCCTCAGCCTCTTCA[A/G]GGCCGGCCCTGCTCC	4297
rs781877164	snp	A/G	1.64942e-05	0.00287173	missense	KMT2A	GRCh38.p7	11:118510058	AAAAAACCCAAGAAA[A/G]GACTTGTTTTTGAAA	4297
rs781877382	snp	A/G	1.65974e-05	0.0028807	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519831	GCAGTTTTGGGTCTC[A/G]ATTTTCTTATCTCAT	4297
rs781878057	snp	C/T	1.65029e-05	0.00287248	missense	KMT2A	GRCh38.p7	11:118495795	GCCACACTGAGCAGC[C/T]TCCTTTAATGAAGAA	4297
rs781878460	snp	G/T	1.64792e-05	0.00287042	missense	KMT2A	GRCh38.p7	11:118504029	GAGGAGGAACAGTGT[G/T]ATCTTCCAAAAATCT	4297
rs781879065	snp	A/C	1.66211e-05	0.00288275	intron-variant	KMT2A	GRCh38.p7	11:118489899	CTGGGTGAGTTATAC[A/C]CATGATGCTCTTTTA	4297
rs781879283	in-del	-/T			intron-variant	KMT2A	GRCh38.p7	11:118481190	CTAGATCTCATTCAC[-/T]TCTATCTAGCTATAT	4297
rs781881705	snp	C/T	1.98714e-05	0.00315203	intron-variant	KMT2A	GRCh38.p7	11:118491941	CAGGTAGGCCAAGTC[C/T]CATTTTTTTCTGAGA	4297
rs781881717	snp	A/T	1.65236e-05	0.00287429	intron-variant	KMT2A	GRCh38.p7	11:118493256	ACAGTGAGCCATCAG[A/T]ATTTCTAGTGCCAAT	4297
rs781881985	snp	A/G	3.32364e-05	0.00407641	missense	KMT2A	GRCh38.p7	11:118498509	ATTGCCAACGACATC[A/G]GGATTTGATCAAAGG	4297
rs781882727	snp	G/T	1.84879e-05	0.00304033	intron-variant	KMT2A	GRCh38.p7	11:118471643	TATATGCTCTTCATT[G/T]TTTAATTTCTATACA	4297
rs781882766	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118518133	ACCATTACTGTTTCT[A/G]TATCTATTAATAATA	4297
rs781883825	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118500125	AAGTATTATTGACAT[A/G]ATTTCAGAATTACTT	4297
rs781883834	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118450770	GAGAGAATCTGCCCT[C/T]GTTCCTGCCCCTGAC	4297
rs781884348	snp	A/T	1.64806e-05	0.00287054	missense	KMT2A	GRCh38.p7	11:118474181	ACTTCCTCCATAGGC[A/T]CCATGTTGGCTCAGG	4297
rs781884825	snp	A/G	1.64757e-05	0.00287012	missense	KMT2A	GRCh38.p7	11:118506504	GTGCCGGGTCCCACT[A/G]AACCCAAACCAAAAA	4297
rs781886915	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118455738	GGTCTCACTCTGTTA[A/T]CCAGGCTGGAGTTCA	4297
rs781886946	snp	A/G/T	0.000115317	0.00759253	missense	KMT2A	GRCh38.p7	11:118505740	ATACTTCATCTCACC[A/G/T]AACTGTCCCCAACAT	4297
rs781887338	snp	A/G	1.66807e-05	0.00288792	missense, intron-variant	KMT2A	GRCh38.p7	11:118473726	AAGACAAGGCCCCCG[A/G]GGAGCTGTCCAAAGA	4297
rs781887574	snp	A/C	1.64811e-05	0.00287059	missense	KMT2A	GRCh38.p7	11:118499411	CCAGAAAATATCCAC[A/C]TGATGATTGGTATGA	4297
rs781888074	snp	A/T	1.6498e-05	0.00287206	synonymous-codon, nc-transcript-variant, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519619	TCTGATTCTTCTAGG[A/T]GTTAACGGTTTGAGG	4297
rs781888203	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118453624	TTCTCTAACACTGAC[C/T]ACTTCTCAGAGTTCC	4297
rs781888216	in-del	-/ACCT			intron-variant	KMT2A	GRCh38.p7	11:118460532	GAGCTCAAGCAATCC[-/ACCT]ACCTGCCTTGGCCTC	4297
rs781889183	snp	A/G	1.71484e-05	0.00292812	intron-variant	KMT2A	GRCh38.p7	11:118501631	TTGTTTGATATTTTA[A/G]TTGGGCCTTTTTAGT	4297
rs781889756	snp	A/C	1.64749e-05	0.00287005	missense	KMT2A	GRCh38.p7	11:118505592	CTACAGACCCGAAAG[A/C]ATAAAAAACTTGCTC	4297
rs781891521	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118507159	TTAAAACAGCTGGGT[A/G]TGGTGTTGCACACCT	4297
rs781891897	snp	C/T	1.6513e-05	0.00287336	synonymous-codon	KMT2A	GRCh38.p7	11:118502678	TAGTTTAGGGCAAAA[C/T]ACTTCCACCTCTTCA	4297
rs781891929	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118501522	GATTCAGGGAGTACT[A/G]TGATTGAAAGCTGGG	4297
rs781892445	snp	A/C/T	3.42403e-05	0.00413753	intron-variant	KMT2A	GRCh38.p7	11:118507637	ATTCGTCTTTTAAGA[A/C/T]TAAGCTCTCAGTTTT	4297
rs781892517	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118443396	GTTAAATATTTCAAT[A/G]AGTTTTTTACCTTGT	4297
rs781892796	snp	A/G			intron-variant, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519413	TTTTTTCACTTAGCC[A/G]TCTATCACAAACATT	4297
rs781893618	snp	A/G	1.66366e-05	0.0028841	intron-variant	KMT2A	GRCh38.p7	11:118497893	GGAAAACCTCCTTTG[A/G]CATTATATTCTTTAG	4297
rs781894017	snp	A/G	3.29924e-05	0.00406142	synonymous-codon	KMT2A	GRCh38.p7	11:118499908	GCTCTTTCCTATTGG[A/G]TATCAGTAAGTAGCA	4297
rs781894404	snp	A/G	1.6501e-05	0.00287232	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473496	TTCTGTCTCTTCCTC[A/G]TTAAGCATTTCTGTT	4297
rs781894433	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118460198	CCTAGTTACAATACT[A/G]AGGAATGGAGATATA	4297
rs781894940	snp	A/T	1.73327e-05	0.00294381	intron-variant	KMT2A	GRCh38.p7	11:118507495	ATATTTACTGGTGGT[A/T]TGTCTTGAAAAGATA	4297
rs781895419	snp	C/G	6.59141e-05	0.00574045	missense	KMT2A	GRCh38.p7	11:118504895	TTTTATCCAAGGACA[C/G]ATGGATGCAGACCAC	4297
rs781896383	snp	A/G	3.29451e-05	0.00405851	missense	KMT2A	GRCh38.p7	11:118505899	CAGGGTCTGTGTCTG[A/G]CTTGGCATCCAGTTC	4297
rs781896727	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118467460	AATAGTCCAATACTT[C/T]AATCTTAGCAATCTC	4297
rs781896757	snp	C/T	1.64781e-05	0.00287033	synonymous-codon	KMT2A	GRCh38.p7	11:118477986	GTCATCAATTGCTGG[C/T]TCAGAAGATGCTGAA	4297
rs781896886	snp	A/G	4.94409e-05	0.00497172	missense, intron-variant	KMT2A	GRCh38.p7	11:118473992	GATTCTGGGACTGAT[A/G]TTACTTCTGTGACTC	4297
rs781897465	snp	C/T	1.64814e-05	0.00287061	missense	KMT2A	GRCh38.p7	11:118501804	CCAGGATTCGAACAC[C/T]CAGTTATTCTCCAAC	4297
rs781897852	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520164	ATCAGAATTTCCTGG[A/G]TAAGATTTAAAAGGA	4297
rs781900175	snp	C/G	1.64985e-05	0.0028721	missense	KMT2A	GRCh38.p7	11:118502857	AGAGCTCAGAGGGAT[C/G]TGCACATAATGTGGC	4297
rs781900312	snp	A/G	2.79943e-05	0.00374117	intron-variant, missense	KMT2A	GRCh38.p7	11:118439068	AACCAAAGGCCACAT[A/G]CATGACAAAAAGACT	4297
rs781900603	snp	A/G	3.39512e-05	0.00412001	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118472092	TCCATCAACAGAAAG[A/G]ATAAAGACCCCTTCG	4297
rs781902838	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118446017	TCCAAAAAAAAGAAA[G/T]AAAAAAAGAAAAGTA	4297
rs781902954	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118490747	AGAAAATTTATGAAG[G/T]TTATACAGAGTACTG	4297
rs781903029	snp	C/T	1.64779e-05	0.00287031	missense	KMT2A	GRCh38.p7	11:118505439	CCAAACATCAGCAAT[C/T]CTCCTTCAGGCCTGC	4297
rs781903097	snp	C/T	3.30115e-05	0.00406259	synonymous-codon	KMT2A	GRCh38.p7	11:118484867	CTCTCCACAGGAGGA[C/T]TGTGAAGCAGAAAAT	4297
rs781903399	snp	G/T			upstream-variant-2KB, downstream-variant-500B, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118527034	TTCATCAGTGATGTA[G/T]GTTCAGGACCTAATT	4297
rs781903452	snp	C/G	1.64768e-05	0.00287021	missense	KMT2A	GRCh38.p7	11:118506242	TTCTGGGGAAGCAGA[C/G]GAACACTATCAGCTT	4297
rs781903822	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118438388	GGTTCAGCCAGTGGC[A/G]TTGCGCATTTGTTTT	4297
rs781904316	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118439170	CAGCAAAAAAAAAAA[A/G]AAAGAAAAAAAAGAA	4297
rs781904444	snp	C/T	1.64787e-05	0.00287038	missense, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521293	TTTGTCCTAGGTCTC[C/T]CATCCATGGCCGGGG	4297
rs781904699	snp	C/T	1.6528e-05	0.00287467	intron-variant	KMT2A	GRCh38.p7	11:118493054	TATCTTTCCTGGCAA[C/T]AGGCTGCCAAGCCTC	4297
rs781906309	snp	C/T	1.68903e-05	0.00290601	intron-variant	KMT2A	GRCh38.p7	11:118476764	CAGTTATAATTTCAA[C/T]ATGTATGGTTGTTAT	4297
rs781906517	snp	A/C	0.000109727	0.00740619	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118435104	GTCCAGGAAGGCTGC[A/C]TGACCTTCCAGCGAA	4297
rs781907666	snp	A/G	2.55196e-05	0.003572	intron-variant	KMT2A	GRCh38.p7	11:118488524	TGCCAGTGGACTACT[A/G]AAACCCAAAGTATAT	4297
rs781908837	snp	A/G	1.96817e-05	0.00313695	intron-variant	KMT2A	GRCh38.p7	11:118482127	AGGAATTGCTGAACC[A/G]CAAGTACTAACAAAA	4297
rs781908849	snp	C/T	1.68182e-05	0.00289979	missense	KMT2A	GRCh38.p7	11:118490193	GCAAAGGGTGGGATG[C/T]ACAGTGGTCTCATGA	4297
rs781909350	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118477247	GAAGGCAGAATCTTC[C/T]TAGACTGCTGTGCAG	4297
rs781910930	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118478693	GACAATTCAGGAAAC[A/G]TTGGAGATACCTTGC	4297
rs781911547	snp	A/G	1.64768e-05	0.00287021	synonymous-codon	KMT2A	GRCh38.p7	11:118503725	CCCCAAACCTCAGGA[A/G]GATGGCTCTTTTAAA	4297
rs781911944	snp	C/G	1.6476e-05	0.00287014	missense	KMT2A	GRCh38.p7	11:118502983	CAGTGTCGTTTTCTT[C/G]TAAAGAGGCCCTCTC	4297
rs781912210	snp	A/T	4.95381e-05	0.0049766	synonymous-codon	KMT2A	GRCh38.p7	11:118505531	AGACCTCAGTACCAC[A/T]GTAGCCACTCCATCC	4297
rs781915159	snp	A/C	1.64803e-05	0.00287052	missense	KMT2A	GRCh38.p7	11:118502497	GTCACAGTACCTCTT[A/C]CTTATCACCCCAGCG	4297
rs781915176	snp	G/T			intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118511876	ATTCTAAGCAGTGCT[G/T]GTGCACATCATTGGT	4297
rs781915476	snp	G/T	1.66043e-05	0.00288129	intron-variant	KMT2A	GRCh38.p7	11:118477918	TACCAATTAAAACCA[G/T]GTTTGAATTCAGTAC	4297
rs781916022	snp	C/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521100	GCTTCCAGCGGGTCA[C/T]AGAATGGAAATAACT	4297
rs781917086	snp	C/T	8.49533e-05	0.00651686	synonymous-codon	KMT2A	GRCh38.p7	11:118436749	TCCAGGGGGAGCGGC[C/T]GCCGCCTCAGCAGCC	4297
rs781917809	snp	C/G	1.68832e-05	0.00290539	intron-variant	KMT2A	GRCh38.p7	11:118501174	ATCAAGATGGGACTT[C/G]AGGCTGGGCACAGTG	4297
rs781918846	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118476386	AAGCTTAGTTGTTTG[C/T]TTGTTTTTAAGATAG	4297
rs781919296	snp	A/G	1.64811e-05	0.00287059	missense	KMT2A	GRCh38.p7	11:118503021	CACCTCCATTTGAGA[A/G]GGCAAAGGAATGATC	4297
rs781919638	snp	A/T	1.64741e-05	0.00286998	missense	KMT2A	GRCh38.p7	11:118499372	GGAATCAGCTTGAGA[A/T]GGAAGTTTCTCAATG	4297
rs781919840	snp	C/T	1.64732e-05	0.0028699	missense	KMT2A	GRCh38.p7	11:118506309	ATTCATTCTTCCCAG[C/T]GTGATCTTGATTCTG	4297
rs781920014	snp	C/G/T	3.30831e-05	0.00406702	missense	KMT2A	GRCh38.p7	11:118507578	GCTAGCGTGGAGCAG[C/G/T]CCTCCCAGAAGGAGT	4297
rs781920905	snp	C/G	1.64789e-05	0.0028704	synonymous-codon	KMT2A	GRCh38.p7	11:118504832	TGACCCAGCACTGCT[C/G]AGCCCAGGAGTAGAT	4297
rs781921088	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118506770	TACCTGGGAGTTTTC[C/T]GGGTTTTGACTTTTT	4297
rs781922324	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118470685	TAGCAAGCAGTTCCA[C/T]TGTAAAAATGTTCAT	4297
rs781922536	snp	A/C/T	4.94208e-05	0.00497075	missense, synonymous-codon	KMT2A	GRCh38.p7	11:118501772	CTCCTGTTATTATCA[A/C/T]GTCATCTCAAAGGTC	4297
rs781922583	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118487983	CAGGAGATTGAGACC[A/G]TCCTCGCTAACACAG	4297
rs781922604	snp	C/T	1.67077e-05	0.00289026	intron-variant	KMT2A	GRCh38.p7	11:118489773	ATGCTTATCTTTTTG[C/T]CATTATATTTTCTTA	4297
rs781923821	snp	A/G	1.64751e-05	0.00287007	synonymous-codon	KMT2A	GRCh38.p7	11:118502612	CGCTACTGATCTTGA[A/G]TCAAGTGCCAAAGTA	4297
rs781923848	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118445395	GTTGCTACCTGTTGT[C/T]TCTATAACTAGTGTT	4297
rs781924648	snp	C/T	1.64806e-05	0.00287054	synonymous-codon	KMT2A	GRCh38.p7	11:118484242	GAACATCCTCAGCAC[C/T]CTCTCCAATGGCAAT	4297
rs781924864	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118499522	GGTGTGGTGTCTCAC[A/G]CCTGTAATCCCAGCA	4297
rs781925188	snp	A/G	1.64773e-05	0.00287026	missense	KMT2A	GRCh38.p7	11:118503993	GGAGAGGAACGACTG[A/G]CATCCCATAATTTAT	4297
rs781925449	snp	A/G	1.65282e-05	0.00287469	missense	KMT2A	GRCh38.p7	11:118481906	AGTGAAGAAGGGAAT[A/G]TCTCGGCCCCTGGGC	4297
rs781926193	snp	A/G	5.13633e-05	0.00506744	intron-variant	KMT2A	GRCh38.p7	11:118478242	GTTGACCTCTCAACC[A/G]TAAAGGTTGCTTATT	4297
rs781926658	snp	C/G	1.66205e-05	0.00288271	intron-variant, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519587	CTGTTGACTGCGCTC[C/G]TCACTTCCCTGGTGC	4297
rs781926768	snp	C/T	3.30207e-05	0.00406316	missense	KMT2A	GRCh38.p7	11:118502838	ACCAAAGTGCTGAGT[C/T]CCAAGAGCTCAGAGG	4297
rs781927232	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118482753	TGTCTTTATTTAAAC[-/A]AAAAAAAAAAAAAGA	4297
rs781927823	snp	A/T	8.26767e-05	0.00642896	missense	KMT2A	GRCh38.p7	11:118503211	CCTGTAAAGAAACTT[A/T]CAAAGAAAAGCATTC	4297
rs781928099	snp	A/G	1.64974e-05	0.00287201	synonymous-codon	KMT2A	GRCh38.p7	11:118504505	GGGTGAGAGCCCAGA[A/G]TCATCTTCATCAGAA	4297
rs781928900	snp	C/G	1.64955e-05	0.00287184	missense, intron-variant	KMT2A	GRCh38.p7	11:118473457	GCTTAGTAGTTCTGA[C/G]CTCTCACCTCTCACC	4297
rs781929360	snp	C/G	3.29587e-05	0.00405934	missense	KMT2A	GRCh38.p7	11:118505223	CAATTGACCTCTTCT[C/G]TTAGTTCTACACCCA	4297
rs781929665	snp	A/G	1.86956e-05	0.00305736	intron-variant	KMT2A	GRCh38.p7	11:118490103	AAACAAGAAATTCCT[A/G]TTGAATTTCTTTTCT	4297
rs781929937	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118467913	GTCTGTCTCTGGAAA[G/T]AACTCAATCTCTGAA	4297
rs781930829	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118437981	CCACCCACTGCGCCT[A/G]AGAGCACGCAGTCTC	4297
rs781930926	snp	C/T	1.65897e-05	0.00288003	intron-variant	KMT2A	GRCh38.p7	11:118488481	TTACATAGTCATTGC[C/T]TAATGAATATGTATT	4297
rs781931131	snp	A/G	1.67388e-05	0.00289294	intron-variant	KMT2A	GRCh38.p7	11:118468705	TTGTGTCTCCTCTGG[A/G]CATTTCTTTGGGATG	4297
rs781933086	snp	C/T	1.73429e-05	0.00294468	synonymous-codon	KMT2A	GRCh38.p7	11:118482076	CAAGAAAAAGCAGCC[C/T]CCACCACCAGAATCA	4297
rs781933899	snp	A/G	8.27096e-05	0.00643024	missense, intron-variant	KMT2A	GRCh38.p7	11:118472349	CTCAGCTGCAGGGAA[A/G]AAAGGTGAAGACACA	4297
rs781934055	snp	G/T	1.64909e-05	0.00287144	missense	KMT2A	GRCh38.p7	11:118504229	TGTTGGCCACAAAAA[G/T]GAGCCAAAGATGGAT	4297
rs781934256	snp	C/T	1.64855e-05	0.00287097	missense, intron-variant	KMT2A	GRCh38.p7	11:118472832	CCCAGCAGCAGACCT[C/T]CTCGTCTCCACCTCC	4297
rs781934381	snp	C/T	1.65636e-05	0.00287776	synonymous-codon	KMT2A	GRCh38.p7	11:118491887	GTTCTGACAGCTTTG[C/T]TGAATTCTCGGACTA	4297
rs781934445	snp	A/G	1.73441e-05	0.00294478	intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118511914	AGGGTTTACGTGCAT[A/G]TTTTCTGGCTTACGG	4297
rs781935868	snp	A/T	3.31868e-05	0.00407336	intron-variant	KMT2A	GRCh38.p7	11:118491154	CGTAAAAACACGGGT[A/T]TGTGAGCCAAAGCAC	4297
rs781936012	snp	G/T	1.67063e-05	0.00289014	synonymous-codon	KMT2A	GRCh38.p7	11:118495874	AACTCCTCTGCATCC[G/T]CCTACACCACCAATT	4297
rs781936584	snp	C/T	1.69951e-05	0.00291501	intron-variant	KMT2A	GRCh38.p7	11:118484833	GTGTAATTGTAAAAC[C/T]TTCCTAAGTGACCTT	4297
rs781937325	snp	A/G	3.29495e-05	0.00405877	missense	KMT2A	GRCh38.p7	11:118488686	GAGCGCCCTCTGGAG[A/G]ACCAGCTGGAAAATT	4297
rs781937357	snp	A/G	1.6563e-05	0.00287771	missense, intron-variant	KMT2A	GRCh38.p7	11:118471811	AAAGATTCTAAAAGT[A/G]TAGAAAAGAAGAGAG	4297
rs781938256	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118461965	TTATTTATTTATTTA[A/T]TTTTGAGACGGAGTT	4297
rs781938682	snp	A/T	0.000162061	0.00900025	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118434978	GCGTGAAGTGCACCC[A/T]CCGGAGGGCCAGAGC	4297
rs781939042	snp	C/G	1.87345e-05	0.00306054	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520081	TAAGTCTTGAGTGGG[C/G]AGCAGTCATTAGAAA	4297
rs781939416	snp	C/G	1.69418e-05	0.00291043	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118472023	TAAGTTTAAGACAGG[C/G]AAGCTTCAAATAGGA	4297
rs781939861	snp	G/T	1.6476e-05	0.00287014	missense	KMT2A	GRCh38.p7	11:118503410	CAAAGCTCCACCCAT[G/T]CAAGTAGAAGGATCT	4297
rs781939908	in-del	-/T	2.01153e-05	0.00317131	intron-variant	KMT2A	GRCh38.p7	11:118491943	GTAGGCCAAGTCTCA[-/T]TTTTTTTCTGAGAGC	4297
rs781940332	snp	C/T			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118523114	GCTCCATGGAGAGTT[C/T]TAAAGAAACATATGT	4297
rs781941668	snp	A/C	6.63669e-05	0.00576013	missense	KMT2A	GRCh38.p7	11:118474283	ATTGAGAAGAGTAAG[A/C]GTCTTAAACAAACCG	4297
rs781941851	snp	C/T	5.11967e-05	0.00505922	synonymous-codon	KMT2A	GRCh38.p7	11:118436920	CGTGTTTGGGGAGAG[C/T]GGCGGGGGAGGCGGC	4297
rs781942657	snp	C/T	3.36067e-05	0.00409905	intron-variant	KMT2A	GRCh38.p7	11:118507615	AACCTGCAGGGTAAG[C/T]TGAAGAATTCGTCTT	4297
rs781943198	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118489775	GCTTATCTTTTTGCC[A/G]TTATATTTTCTTACA	4297
rs781944045	snp	A/G			upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118525558	CTCCGTCAAACCCCC[A/G]GCCAATGCAGTGAGC	4297
rs781944403	snp	A/C/G	3.85136e-05	0.00438812	missense	KMT2A	GRCh38.p7	11:118494397	AGTCCTTCTTCATTC[A/C/G]GGTGAATGATATTAC	4297
rs781944987	snp	A/G	6.7587e-05	0.00581282	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522211	GGAGTGCAAGGAGGC[A/G]GGGCCATCCAAAGCA	4297
rs781945114	snp	A/G	1.66674e-05	0.00288676	intron-variant	KMT2A	GRCh38.p7	11:118493033	TAGTGTTAGATAAAA[A/G]CAACATATCTTTCCT	4297
rs781945281	snp	A/G	9.88338e-05	0.00702902	missense, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519717	GAAATTACAAATTCC[A/G]TTTCCACAAGCCAGA	4297
rs781947198	snp	A/G	1.74427e-05	0.00295314	intron-variant	KMT2A	GRCh38.p7	11:118507480	CTCCACATTCAGTAC[A/G]TATTTACTGGTGGTT	4297
rs781948266	snp	C/G	1.65463e-05	0.00287626	missense	KMT2A	GRCh38.p7	11:118509984	AGGAAAGTAATTTCA[C/G]CTCCCCACTGATGCT	4297
rs781948454	snp	A/G	3.29462e-05	0.00405857	missense	KMT2A	GRCh38.p7	11:118505858	AGGCACATCAACAAT[A/G]AGCCAGGATACTAGC	4297
rs781948619	snp	G/T	1.66579e-05	0.00288595	missense, intron-variant	KMT2A	GRCh38.p7	11:118473284	CCAAGTGAGGCTCAC[G/T]CTAGAATATTTGAGT	4297
rs781948984	snp	C/T	1.6476e-05	0.00287014	synonymous-codon	KMT2A	GRCh38.p7	11:118491790	AGAAAGTGTGGCCTA[C/T]ACTTGTGTGAACTGT	4297
rs781949220	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118497654	CCTACCACTTCAGCC[A/T]CCAAAAGTGCTGGGA	4297
rs781949543	snp	C/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118515952	CTTGGCCTCCCAAAG[C/T]GCTGAGAGTACAGGT	4297
rs781949883	snp	A/G	1.65113e-05	0.00287322	missense, intron-variant	KMT2A	GRCh38.p7	11:118473819	AGGAGAATAAGCGGG[A/G]GTCAAGGAAAGAGAA	4297
rs781950327	snp	C/T	3.29462e-05	0.00405857	missense	KMT2A	GRCh38.p7	11:118496312	ACCCACCCCCAGGCA[C/T]AGAAGACAATAGACA	4297
rs781950365	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118463816	GAATTTCAAAATTTT[A/G]TATGCACCAAAATAA	4297
rs781950848	snp	C/T	3.34392e-05	0.00408883	synonymous-codon	KMT2A	GRCh38.p7	11:118509145	ATTTAGGCAAGTCGC[C/T]GTTCTTCCGGAAGTT	4297
rs781951109	in-del	-/G	0.000119753	0.00773707	intron-variant	KMT2A	GRCh38.p7	11:118439167	AGCAGCAAAAAAAAA[-/G]AAAAAAGAAAAAAAA	4297
rs781951838	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118443892	TTTCTTGCATTTCTG[A/G]TTTTGTGTTTTGTTG	4297
rs781952112	snp	C/T	1.65056e-05	0.00287272	intron-variant	KMT2A	GRCh38.p7	11:118499826	ATCGGTTCTTCTTTC[C/T]TTGGTCAGGGTCTAT	4297
rs781952152	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118484619	AGTCAGCAAAACTGT[-/A]AGAGAAATTCAATCC	4297
rs781952663	snp	A/G	0.00018143	0.00952271	missense	KMT2A	GRCh38.p7	11:118495773	TGGCAGGAGCGAGAG[A/G]AAAACAGCCACACTG	4297
rs781953449	snp	A/G	1.87647e-05	0.00306301	intron-variant	KMT2A	GRCh38.p7	11:118471631	TACACAGCTAAATAT[A/G]TGCTCTTCATTGTTT	4297
rs781953915	snp	A/C			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521840	AGATTGGGACATGTT[A/C]TTAAAGCTGAGTTTA	4297
rs781955393	snp	A/T			missense	KMT2A	GRCh38.p7	11:118510020	TTCAGCAAGAACAAA[A/T]GCGGAAGGAAAGCAT	4297
rs781955490	snp	A/G	1.6476e-05	0.00287014	synonymous-codon	KMT2A	GRCh38.p7	11:118505720	GTTAGATTTGGGGTC[A/G]CTTAATACTTCATCT	4297
rs781955604	snp	C/T	0.000182033	0.00953853	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118472602	CTCTCGATCTAGTAG[C/T]CCCAGTGTTGATACC	4297
rs781956004	snp	C/T	3.33456e-05	0.0040831	intron-variant	KMT2A	GRCh38.p7	11:118500952	CTGCTTCTATCCTCT[C/T]CCTTATGATGATTTT	4297
rs781956838	snp	A/G	1.64738e-05	0.00286995	synonymous-codon	KMT2A	GRCh38.p7	11:118498031	AGATGATGACGGATC[A/G]CTAAAGAATGTGCAT	4297
rs781957536	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118438554	TTGAAACAGAAAGGG[A/G]AAGATAACAACCAGC	4297
rs781959189	snp	A/G	0.000181331	0.00952012	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473043	GCATTCTAGGTCAGA[A/G]CCACAATACTTTTCC	4297
rs781959322	snp	G/T	4.49711e-05	0.00474168	synonymous-codon	KMT2A	GRCh38.p7	11:118436782	CTCGTCGTCCGCCTC[G/T]TCTTCGTCTTCGTCA	4297
rs781959523	snp	C/T	1.64741e-05	0.00286998	missense	KMT2A	GRCh38.p7	11:118505041	AGAACCAGAAGTATG[C/T]GCCCAATTCTACTGA	4297
rs781960499	snp	A/T	1.64746e-05	0.00287002	missense	KMT2A	GRCh38.p7	11:118502933	ATCTAGAGAACTGAA[A/T]GTTAGTAAAATCGGC	4297
rs781960530	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118442262	TTGTGACTATCACTA[C/T]TTTGGGAGGAATTTA	4297
rs781961490	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118485558	TGGTGGAAAGAAATA[C/T]AGATTAGTTACAATC	4297
rs781961869	snp	C/T	1.64906e-05	0.00287142	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473052	GTCAGAGCCACAATA[C/T]TTTTCCTCAGCAAAG	4297
rs781961947	snp	C/G	1.71634e-05	0.0029294	intron-variant	KMT2A	GRCh38.p7	11:118501892	TACTTGACCTAAGAA[C/G]ATCAGCCCAAAGACT	4297
rs781963873	snp	A/G	1.65773e-05	0.00287895	missense	KMT2A	GRCh38.p7	11:118506577	AGCACAAAGTTTCCC[A/G]TTTGCGGACCAGTTC	4297
rs781965108	snp	C/T	1.65397e-05	0.00287569	synonymous-codon	KMT2A	GRCh38.p7	11:118498459	CATGTGTTCCCGAGC[C/T]AAGAACTGTGTCTTT	4297
rs781965936	snp	A/G	1.65233e-05	0.00287426	intron-variant	KMT2A	GRCh38.p7	11:118468863	CGGCCAATTAAGTGC[A/G]TGGTGCCTTTTAAGT	4297
rs781966368	snp	C/T			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522324	TATGTCCTATACTCA[C/T]ATCAGACATGTGATC	4297
rs781967523	snp	A/T	4.96134e-05	0.00498039	synonymous-codon	KMT2A	GRCh38.p7	11:118504121	GAAAAGCAGCCAGAT[A/T]CCAAAAAGAAATGGT	4297
rs781967539	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118464156	CTTGTTCATGCCGTA[A/G]TTGAAGAGGAATGAT	4297
rs781968103	snp	A/G	3.30038e-05	0.00406212	missense	KMT2A	GRCh38.p7	11:118506093	CAGGACCAGCCTGTG[A/G]CTTTACCGCCAAGTT	4297
rs781968542	snp	C/T	4.94645e-05	0.00497291	synonymous-codon	KMT2A	GRCh38.p7	11:118503047	TGATCGAGACCAACA[C/T]ACAGATTCTACCCAA	4297
rs781968810	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118449519	TGAGCCCAATGGGTC[A/G]AGGCTGCAGTGAGCC	4297
rs781969976	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118480443	AATTTTCCATAATAA[A/T]TTTTTTAAATTTATA	4297
rs781970017	snp	G/T	1.64727e-05	0.00286986	intron-variant	KMT2A	GRCh38.p7	11:118491729	CCTCATCATGGTAGG[G/T]TTTTGTTTTCTTAGA	4297
rs781970154	snp	A/G	1.64787e-05	0.00287038	intron-variant	KMT2A	GRCh38.p7	11:118488610	TCCCATGTTCTTACT[A/G]TAGTTTGTGTATTGC	4297
rs781970936	snp	G/T	1.64885e-05	0.00287123	missense	KMT2A	GRCh38.p7	11:118504780	CAGGGGAGAAGAGAG[G/T]AACCATCACAGAAAA	4297
rs781971174	in-del	-/TTTG			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118517881	ACAACATTCTTTTTG[-/TTTG]TTTGTTTGTTTGTTT	4297
rs781971827	snp	G/T	1.64792e-05	0.00287042	missense	KMT2A	GRCh38.p7	11:118505525	GAGGACAGACCTCAG[G/T]ACCACAGTAGCCACT	4297
rs781972734	snp	C/T	4.94442e-05	0.00497188	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473976	GAAGTCTTCATCACA[C/T]GATTCTGGGACTGAT	4297
rs781973183	snp	A/G	3.29625e-05	0.00405958	missense	KMT2A	GRCh38.p7	11:118484250	TCAGCACTCTCTCCA[A/G]TGGCAATAGTTCTAA	4297
rs781973852	snp	A/C	0.000153504	0.00875947	synonymous-codon	KMT2A	GRCh38.p7	11:118436590	CGGGGGGCGCCGGGG[A/C]CTAGGGGGCGCCCCG	4297
rs781973902	snp	C/T	1.65321e-05	0.00287502	synonymous-codon	KMT2A	GRCh38.p7	11:118503227	CAAAGAAAAGCATTC[C/T]AGTAAATCTTTTTTG	4297
rs781974413	snp	A/G	1.64814e-05	0.00287061	missense	KMT2A	GRCh38.p7	11:118502637	AAAGTAGTTGATCAT[A/G]TCTTAGGGCCACTGA	4297
rs781975229	snp	A/G	8.24627e-05	0.00642063	intron-variant	KMT2A	GRCh38.p7	11:118477962	ATGCCACATTTCTTT[A/G]ACAGACAAGTCATCA	4297
rs781976352	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118456832	AACATTTCAAATTCA[C/G]ATGTCTAAAATGATC	4297
rs781976863	snp	A/G	1.64996e-05	0.0028722	missense	KMT2A	GRCh38.p7	11:118505302	TCACCCTTACCACAG[A/G]ACTAAATCCAAGCTT	4297
rs781977882	snp	C/T	1.64732e-05	0.0028699	synonymous-codon, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522088	AGAGGAACTCACTTA[C/T]GACTATAAGTTCCCC	4297
rs781978013	snp	A/G	1.65299e-05	0.00287483	missense, intron-variant	KMT2A	GRCh38.p7	11:118472681	CGGAGCGATACCCCT[A/G]AAGTTCATCCTCCAC	4297
rs781978595	snp	A/G	3.39236e-05	0.00411833	missense, intron-variant	KMT2A	GRCh38.p7	11:118472061	GGGTACAAATTGTAC[A/G]ACGGAGAGGAAGGCC	4297
rs781980190	snp	A/T	1.64749e-05	0.00287005	missense, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521398	AGACTGACAAGCGGG[A/T]AAAGTATTACGACAG	4297
rs781980227	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118506890	GCTCTGATTTCAAAC[A/C]GTGTTGCTGTTTGTT	4297
rs781981734	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118461462	ATTTTGCAGTGCTCT[A/G]CTTGGCAAGGGTGTT	4297
rs781982199	snp	G/T	1.65392e-05	0.00287564	splice-acceptor-variant, intron-variant	KMT2A	GRCh38.p7	11:118489791	TTATATTTTCTTACA[G/T]CAGCTGCTGGAGTGT	4297
rs781982867	snp	A/G	1.6566e-05	0.00287797	missense, intron-variant	KMT2A	GRCh38.p7	11:118471862	GGAGTAAAAATCAAA[A/G]TAACACATGGAAAGG	4297
rs781984541	snp	A/G	1.72824e-05	0.00293954	splice-acceptor-variant	KMT2A	GRCh38.p7	11:118495698	GAATCAATTATTTTC[A/G]GCAGTGGGATGTTAC	4297
rs781984702	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118459785	CCCCCGCCCCGGGTT[C/T]AAGCAATTCTCCTTC	4297
rs781985434	snp	C/T	3.29522e-05	0.00405894	missense, intron-variant	KMT2A	GRCh38.p7	11:118473930	AAGATGTTGCCACTT[C/T]ATCTTCTGCCAAAAA	4297
rs781986487	snp	A/G	6.59098e-05	0.00574026	missense	KMT2A	GRCh38.p7	11:118503588	CCAATTTCAGCCTCT[A/G]AAAATCCAGGAGATG	4297
rs781986682	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118509018	TTCTACAGAAAGCCC[C/T]CTGTGGCTCATTTTC	4297
rs781987936	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118442770	TCTAGAGTATTTTCA[A/G]AATAAGATAAAATAG	4297
rs781989219	snp	C/G			intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118518970	GTAGTCCCAGCTACT[C/G]GGGAGGCTGAGGTAG	4297
rs781989300	snp	G/T	1.64743e-05	0.00287	synonymous-codon	KMT2A	GRCh38.p7	11:118506473	ATCTTCTGGACAGCG[G/T]TCAGCAAGCCCTTCA	4297
rs781989747	snp	C/T	4.99954e-05	0.00499952	intron-variant, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519582	GTTTCCTGTTGACTG[C/T]GCTCCTCACTTCCCT	4297
rs781990391	snp	C/T	1.65567e-05	0.00287716	missense	KMT2A	GRCh38.p7	11:118490147	TGTACCAAGTGTGTT[C/T]GCTGTAAGAGCTGTG	4297
rs781990501	snp	C/T	1.64855e-05	0.00287097	missense, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520842	ATGCCCATGCGCTTC[C/T]GGCACTTAAAAAAGA	4297
rs781990814	snp	G/T	1.76241e-05	0.00296846	intron-variant	KMT2A	GRCh38.p7	11:118438997	ATTATTATTTTTTTT[G/T]GAAAGGCCAATTCTG	4297
rs781991205	snp	G/T	1.64732e-05	0.0028699	missense	KMT2A	GRCh38.p7	11:118506327	GATCTTGATTCTGCT[G/T]CAGGGCCCCAGGTAT	4297
rs781991683	snp	A/T	1.65405e-05	0.00287576	missense, intron-variant	KMT2A	GRCh38.p7	11:118472543	GGATCTTCTGAAAAA[A/T]CAAGTGCAGCTTCTC	4297
rs781991854	snp	C/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520920	AAGAATTACAGAAAA[C/T]GAATGCAGTTTTTCA	4297
rs781992422	snp	C/T	1.65647e-05	0.00287786	synonymous-codon	KMT2A	GRCh38.p7	11:118501095	GGATATCAACAGCAC[C/T]GTTGAACATGATGAA	4297
rs781992679	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118467539	TAGTATGCAAAGGCT[A/G]GGCCTTAAATGTTTT	4297
rs781993197	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118497598	AGACAAAGTCTCCCT[A/G]TGTTGCCCAGGCTGG	4297
rs781995178	snp	C/T	1.64732e-05	0.0028699	synonymous-codon	KMT2A	GRCh38.p7	11:118499353	AGTGTTTGTGGACTT[C/T]GAAGGAATCAGCTTG	4297
rs781995207	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118457766	TCGAAAGATTAAGTT[C/T]TCATCCTCTCTGCAA	4297
rs781995221	snp	A/T	1.66877e-05	0.00288852	missense	KMT2A	GRCh38.p7	11:118474299	GTCTTAAACAAACCG[A/T]CCAGCCCAAAGCACA	4297
rs781995666	snp	A/G	1.66186e-05	0.00288254	missense, intron-variant	KMT2A	GRCh38.p7	11:118473189	CCGCTGCTTCAGCCC[A/G]ATTGTTTTCGCCACT	4297
rs781996318	snp	C/T	3.28337e-05	0.00405164	synonymous-codon	KMT2A	GRCh38.p7	11:118436866	CGCGGCGCTGCAGGT[C/T]TCGGCCGCCATCGGC	4297
rs781996431	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118509701	AAAACTATCAGATCG[C/T]CATACTAGAAATTCT	4297
rs781996665	snp	A/T	1.74503e-05	0.00295379	intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118511903	TGGTATTAAGAAGGG[A/T]TTACGTGCATATTTT	4297
rs781996718	snp	C/T			utr-variant-3-prime, intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118525029	TCAGCCTTGAGTCCA[C/T]TGCCAAATTTTCAGC	4297
rs781998336	snp	A/G/T	3.30531e-05	0.00406518	missense	KMT2A	GRCh38.p7	11:118481900	GAAAAGAGTGAAGAA[A/G/T]GGAATGTCTCGGCCC	4297
rs781998887	snp	A/G	4.94376e-05	0.00497156	synonymous-codon	KMT2A	GRCh38.p7	11:118506206	CTCCACTCAGACTAC[A/G]GGCATAACAGCCGCT	4297
rs782000286	snp	C/G	1.64817e-05	0.00287064	missense, intron-variant	KMT2A	GRCh38.p7	11:118472862	CACCTCTGCTGACTC[C/G]ACCGCCACCACTGCA	4297
rs782000341	snp	A/G	1.68386e-05	0.00290155	missense	KMT2A	GRCh38.p7	11:118482047	GAAGTTCCCAAAACC[A/G]CTCCTAGTGAGCCCA	4297
rs782000656	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118483549	AAAAAATAAAAAGTT[C/T]AGGCTTTAGCCTGTT	4297
rs782001089	snp	A/G	1.64757e-05	0.00287012	missense	KMT2A	GRCh38.p7	11:118501732	CTCCATCACCAGACC[A/G]ACCTCCTCATTCACA	4297
rs782001177	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118453191	CAAAACTCCTTGAAA[A/G]TGCTGTGTGTAATTG	4297
rs782001337	snp	C/T	1.64738e-05	0.00286995	synonymous-codon	KMT2A	GRCh38.p7	11:118496349	GTTATGTTTGACTTA[C/T]GGTGATGACAGTGCT	4297
rs782001750	snp	A/C	1.64931e-05	0.00287163	missense	KMT2A	GRCh38.p7	11:118505379	CCCATGTCTCATCAC[A/C]AGCACTTACATTCCT	4297
rs782002766	snp	C/G	1.66382e-05	0.00288424	intron-variant	KMT2A	GRCh38.p7	11:118484348	CATAAAGTATATTGA[C/G]TGTCAAAGACTTTAA	4297
rs782003068	snp	C/T	3.31066e-05	0.00406844	intron-variant	KMT2A	GRCh38.p7	11:118477010	GGTCAATCTTGGAGT[C/T]GGAACAGACTTTTGA	4297
rs782003557	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118499688	GGGAGGCTGAGGCAC[A/C]GGAATCACTTGAACC	4297
rs782004426	snp	C/T	1.654e-05	0.00287571	synonymous-codon	KMT2A	GRCh38.p7	11:118502786	GTCCAGTGCTTCAGA[C/T]TTGGTGTCCAAGAGC	4297
rs782004439	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118445564	AGTGCTGGTCTACAG[A/C]GATCAATGCAAGTAA	4297
rs782004828	snp	C/G	1.65414e-05	0.00287583	synonymous-codon	KMT2A	GRCh38.p7	11:118503197	GAAAGGGAAAAAATC[C/G]TGTAAAGAAACTTTC	4297
rs782006839	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118438184	AAAAAGGATTATCAA[A/G]CAAAGTTATTCCTTA	4297
rs782007598	snp	C/T	1.64942e-05	0.00287173	missense	KMT2A	GRCh38.p7	11:118499841	CTTGGTCAGGGTCTA[C/T]GACAATCGACTGCTT	4297
rs782008257	snp	A/C	1.66194e-05	0.00288261	intron-variant	KMT2A	GRCh38.p7	11:118482514	AGGAGAGATTTGTTT[A/C]TCTGCCATTTCTCAG	4297
rs782008329	in-del	-/T	6.4255e-05	0.00566775	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118436467	GCCTCCCCGCCCCCC[-/T]GTGTTGTCGCCTCTC	4297
rs782008634	snp	A/T	5.05574e-05	0.00502754	intron-variant	KMT2A	GRCh38.p7	11:118478221	GTGGGTGTTTCACTC[A/T]GAGATGTTGACCTCT	4297
rs782008907	snp	G/T	1.65723e-05	0.00287852	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473670	TACTCCTCTCTTCCC[G/T]TGGTTTACCCCAGGC	4297
rs782008943	snp	C/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118516595	GAAGTAAAAGCTCTA[C/T]GAATACAGGTACCTT	4297
rs782009331	snp	A/G			intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118511552	AGGAACAGAGAGGTT[A/G]TGATCTTCCCACAGT	4297
rs782011284	snp	A/G	1.83092e-05	0.0030256	intron-variant	KMT2A	GRCh38.p7	11:118502366	TTTGTTCTATCTACA[A/G]TAGCATTTATTACTT	4297
rs782013311	snp	C/T	1.65023e-05	0.00287244	missense	KMT2A	GRCh38.p7	11:118506087	GGGATTCAGGACCAG[C/T]CTGTGGCTTTACCGC	4297
rs782013681	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118516868	TTAAGAACAGACGGG[A/G]GCCCACACATAATGC	4297
rs782013822	snp	C/T	1.66098e-05	0.00288177	intron-variant	KMT2A	GRCh38.p7	11:118500969	CTTATGATGATTTTC[C/T]CAAATCTGTTTACCC	4297
rs782014369	snp	A/G	1.66219e-05	0.00288283	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118472293	GCAACTCTTACAGAG[A/G]GCAAAAAAGGGGGCT	4297
rs782014564	snp	A/G	1.64743e-05	0.00287	missense	KMT2A	GRCh38.p7	11:118505016	CCTGTTTCCCCAACT[A/G]TTCCCATCCAGAACC	4297
rs782014615	snp	C/T	0.000118066	0.00768239	intron-variant	KMT2A	GRCh38.p7	11:118490084	AGTTAAGTAAAGATA[C/T]TAAAAACAAGAAATT	4297
rs782015181	snp	C/G	1.64863e-05	0.00287104	missense	KMT2A	GRCh38.p7	11:118504255	TGGATAACTGCCATT[C/G]TGTAAGCAGAGTTAA	4297
rs782015188	snp	A/G	1.66004e-05	0.00288096	intron-variant	KMT2A	GRCh38.p7	11:118468893	TTTTGTTTGTTAGGA[A/G]ATTGTGGCTTCCTCT	4297
rs782015263	snp	C/T	0.000131972	0.0081221	intron-variant	KMT2A	GRCh38.p7	11:118480271	GTCTTCCCCCAAATG[C/T]TCCTTGCTTAAATGG	4297
rs782015794	snp	C/T			upstream-variant-2KB	KMT2A	GRCh38.p7	11:118435126	TCCAGCGAACTCCCC[C/T]TCGGCTTGGGGGATG	4297
rs782015892	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118443658	CAACAAAGATATAAG[A/T]GTTAGTTGGCAGTTT	4297
rs782016574	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118496076	GAGGACTTGATATAA[A/C]TACTCTGGAGTATTG	4297
rs782016740	snp	C/G	1.64768e-05	0.00287021	missense	KMT2A	GRCh38.p7	11:118503438	TCTGCCAAGGAATTA[C/G]AGGCACCACGGAAAC	4297
rs782017800	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118474968	AACCTCATCTCTACT[-/A]AAAAAAAAAAAAAAA	4297
rs782018357	snp	C/G	1.64784e-05	0.00287035	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520097	AGCAGTCATTAGAAA[C/G]TGCTTTCCCTCTCCT	4297
rs782019001	snp	C/T	1.6473e-05	0.00286988	synonymous-codon, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522022	TCGGGTCATCAATAT[C/T]GATGGGCAGAAGCAC	4297
rs782019032	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118489945	TGACTATTGGACTTA[C/T]GTAACTTGTATTACA	4297
rs782019308	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118458309	AACTAGGCTGGTCTA[C/T]AACTCCTGGGCTCAA	4297
rs782021031	snp	G/T			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118523207	GAGTATCACAGCCAG[G/T]ATGACCCTTGGGTCC	4297
rs782021081	snp	C/T	1.64895e-05	0.00287132	missense	KMT2A	GRCh38.p7	11:118484280	AGCAAAAAATTCCAG[C/T]AGATGGAGTCCACAG	4297
rs782022294	snp	C/T	1.65326e-05	0.00287507	synonymous-codon	KMT2A	GRCh38.p7	11:118504112	CACAACAAGGAAAAG[C/T]AGCCAGATTCCAAAA	4297
rs782022323	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118475184	GAAGCACTTAGCCTT[A/G]AGCCATGGAACAGGA	4297
rs782022457	snp	A/C	0.000247539	0.0111224	intron-variant	KMT2A	GRCh38.p7	11:118480283	ATGCTCCTTGCTTAA[A/C]TGGTGTATAGTTGTA	4297
rs782022579	snp	C/T	5.41668e-05	0.00520389	intron-variant	KMT2A	GRCh38.p7	11:118490300	GTTGTACTTGGTGTT[C/T]TGGAGGTGAACTAGA	4297
rs782022978	snp	A/G	1.69456e-05	0.00291075	synonymous-codon	KMT2A	GRCh38.p7	11:118494347	TAATTCAGATGGAGG[A/G]CAGCCAGAAATTAAA	4297
rs782023315	snp	C/G	0.00398008	0.044432	intron-variant	KMT2A	GRCh38.p7	11:118458194	ACTTAAGTGATTCTC[C/G]CACCTCAACCTCCCA	4297
rs782023622	snp	C/T	1.64743e-05	0.00287	missense	KMT2A	GRCh38.p7	11:118505491	CGGATCCCCAACTTT[C/T]GGTTTCAGAATCCAG	4297
rs782024189	snp	A/C	1.69097e-05	0.00290768	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118472002	TAAACTCTCTCCTCT[A/C]AAGTCTAAGTTTAAG	4297
rs782024927	snp	C/T	3.29473e-05	0.00405864	synonymous-codon, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519742	GCCAGAGGAGGCCAA[C/T]GAACCCCCCTTGAAC	4297
rs782025944	snp	A/G	0.000159375	0.00892537	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118434938	TAGGTTTTCAGCACC[A/G]GGAGGCTGTGGACCT	4297
rs782026239	snp	C/T	1.66078e-05	0.00288161	missense	KMT2A	GRCh38.p7	11:118506580	ACAAAGTTTCCCATT[C/T]GCGGACCAGTTCTTC	4297
rs782026475	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118500928	AGAGGTTTTGAAAAA[C/T]GCTAGTTTCTGCTTC	4297
rs782026566	snp	A/G	3.33272e-05	0.00408197	missense, intron-variant	KMT2A	GRCh38.p7	11:118473215	CCACTCCATTCTGGA[A/G]CAAGGTTTGATATGC	4297
rs782028032	snp	A/G	1.64819e-05	0.00287066	missense	KMT2A	GRCh38.p7	11:118504741	CCAGCCAGAATCCCA[A/G]TAGACTAGCTGTTAT	4297
rs782029181	snp	C/G	3.30409e-05	0.0040644	missense, intron-variant	KMT2A	GRCh38.p7	11:118472700	TTCATCCTCCACTGC[C/G]CATTTCCCAGTCCCC	4297
rs782030215	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118464052	GCCCCAAATAAATAA[C/T]TGGATGGCTCATTTT	4297
rs782030378	snp	C/T	1.64732e-05	0.0028699	synonymous-codon	KMT2A	GRCh38.p7	11:118498013	GTCAGCGGAAGTGTT[C/T]GAAGATGATGACGGA	4297
rs782030513	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118483493	AGCCGAGATCGCGCC[-/A]CTGCACTCCAGCTTG	4297
rs782030602	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118470252	CAAGTCTACCACAAT[A/G]GTAAGGAATCTTTTG	4297
rs782030921	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118508374	TCTATTGTGTGGATC[C/T]ACAATATTTTAATGA	4297
rs782031291	snp	A/T	1.66073e-05	0.00288156	synonymous-codon	KMT2A	GRCh38.p7	11:118495730	AAACGCAGTGCTTCC[A/T]CCTTCACTTGACCAT	4297
rs782033469	snp	C/T	1.65847e-05	0.0028796	intron-variant	KMT2A	GRCh38.p7	11:118491739	GTAGGTTTTTGTTTT[C/T]TTAGATGAGATGTAT	4297
rs782033811	snp	C/G	1.64814e-05	0.00287061	synonymous-codon	KMT2A	GRCh38.p7	11:118503905	ACAGGTGGATGGGGC[C/G]GATGACTTAAGCACT	4297
rs782035603	in-del	-/C			intron-variant	KMT2A	GRCh38.p7	11:118508506	TTTGGGAGGCTGAGG[-/C]CAGGAGGATTGCTTG	4297
rs782036702	snp	G/T	1.65441e-05	0.00287607	missense, intron-variant	KMT2A	GRCh38.p7	11:118472579	TCCTCTCAAATGTCT[G/T]CAGACTCCTCTCGAT	4297
rs782037174	snp	A/C			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520754	GATTCAAGACTCAAA[A/C]CATTATTTCCTGAAA	4297
rs782037215	snp	C/G	1.64838e-05	0.00287083	missense, intron-variant	KMT2A	GRCh38.p7	11:118473033	CTTCTTTAAAGCATT[C/G]TAGGTCAGAGCCACA	4297
rs782038033	snp	A/G	1.66346e-05	0.00288393	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473793	TAGAGAGAGAGACCG[A/G]GAGAGAGAAAAGGAG	4297
rs782039100	snp	A/G	3.31428e-05	0.00407066	missense, intron-variant	KMT2A	GRCh38.p7	11:118471877	ATAACACATGGAAAG[A/G]ACATTTCAGAGTTAC	4297
rs782039443	snp	A/T			intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118511712	TTCAGAAGGTCTGAC[A/T]TTCCTTAGTGCTTCT	4297
rs782039577	snp	A/C	1.65326e-05	0.00287507	intron-variant, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519611	CTGGTGCTTCTGATT[A/C]TTCTAGGTGTTAACG	4297
rs782039939	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118454663	CGTTTAATACACTTA[A/C]AAGCTCGTCGTAAAG	4297
rs782040203	in-del	-/T			intron-variant	KMT2A	GRCh38.p7	11:118439926	TGTAGAAGCAAGCAC[-/T]TTTTTTTTTTTTTTA	4297
rs782040269	snp	A/G			missense	KMT2A	GRCh38.p7	11:118503331	AGTATATGGGCCAAC[A/G]ACCATGTAACAATGT	4297
rs782040883	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118444356	ACATCTCTTTAAGCT[C/T]AGCTAATGAGGAAAT	4297
rs782041487	snp	A/G	1.72534e-05	0.00293708	missense	KMT2A	GRCh38.p7	11:118494366	CCAGAAATTAAAAAA[A/G]CCAACAGCATGGTCA	4297
rs782042221	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118510413	GCCATTCCCTCATGC[A/G]CCTTCTGTGCCCTTC	4297
rs782042739	in-del	-/T	3.29701e-05	0.00406005	intron-variant	KMT2A	GRCh38.p7	11:118480244	AAGCTAAAGGTAGTG[-/T]TTGTTAAAAAGGTCT	4297
rs782042971	snp	A/G	1.65592e-05	0.00287738	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473808	GGAGAGAGAAAAGGA[A/G]AATAAGCGGGAGTCA	4297
rs782043365	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118507027	GAAAGCCAAGCACAG[C/T]GGCTCATGTCTGTAA	4297
rs782043967	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118500055	ATTTTGCTAGTTCTC[A/G]GATTCGTCTGCTTGT	4297
rs782043979	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118462026	GCGTGAGCTTTTGGC[C/T]CAATGCAACCTCTGC	4297
rs782044507	snp	C/T	1.65515e-05	0.00287671	synonymous-codon	KMT2A	GRCh38.p7	11:118498429	TCTCACATCCTGCAC[C/T]AGCAACTATCACTTC	4297
rs782044763	snp	C/G	1.66704e-05	0.00288703	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520900	GGTATGACTAAAATT[C/G]TAGAAAGAATTACAG	4297
rs782046765	snp	C/T	1.64849e-05	0.00287092	synonymous-codon	KMT2A	GRCh38.p7	11:118484882	TTGTGAAGCAGAAAA[C/T]GTGTGGGAGATGGGA	4297
rs782046856	snp	C/T	1.64822e-05	0.00287068	missense	KMT2A	GRCh38.p7	11:118505233	CTTCTGTTAGTTCTA[C/T]ACCCAGTGTGATGGA	4297
rs782047584	snp	C/T	2.80147e-05	0.00374254	intron-variant, synonymous-codon	KMT2A	GRCh38.p7	11:118439083	ACATGACAAAAAGAC[C/T]GAACCGTTCAGGTTA	4297
rs782047771	snp	C/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118516742	CTCCCACAAGCAGAA[C/T]AGATTGTTCCTTCTT	4297
rs782047867	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118467925	AAAGAACTCAATCTC[C/T]GAATCATTGAATTTC	4297
rs782047994	snp	C/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118513650	CCCATAGCATGAAAG[C/G]GTACTCAATCTCAGC	4297
rs782049209	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118483778	GCTCACATCTATAAT[-/A]CCCAGCACTTTGGGG	4297
rs782049264	snp	C/G	1.65184e-05	0.00287384	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118472713	GCCCATTTCCCAGTC[C/G]CCAGAAAATGAGAGT	4297
rs782049421	snp	A/G	1.76724e-05	0.00297252	intron-variant	KMT2A	GRCh38.p7	11:118509236	TTAGAATCAGAGAAT[A/G]TCAATGCTAAAAGGA	4297
rs782049484	snp	C/T	1.65446e-05	0.00287612	synonymous-codon	KMT2A	GRCh38.p7	11:118491745	TTTTGTTTTCTTAGA[C/T]GAGATGTATGAGATT	4297
rs782049489	snp	C/T	1.64868e-05	0.00287109	synonymous-codon	KMT2A	GRCh38.p7	11:118504250	AAAGATGGATAACTG[C/T]CATTCTGTAAGCAGA	4297
rs782049684	snp	A/C	1.64762e-05	0.00287016	synonymous-codon	KMT2A	GRCh38.p7	11:118503614	AGATGGTCCAGTGGC[A/C]CAACCAAGCCCCAAT	4297
rs782049886	snp	C/G	1.70237e-05	0.00291746	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118472107	GATAAAGACCCCTTC[C/G]GGTCTCCTCATTAAT	4297
rs782050529	snp	C/T	1.6477e-05	0.00287024	missense	KMT2A	GRCh38.p7	11:118503427	AAGTAGAAGGATCTG[C/T]CAAGGAATTACAGGC	4297
rs782052879	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118447325	GGTGACTTTTTATAT[A/G]GTATTTGTTGAATTG	4297
rs782054087	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118453478	AGTATTCTGTATGGC[C/T]TCCCTCCTCTGCTTA	4297
rs782055040	snp	A/G	0.000247621	0.0111243	missense	KMT2A	GRCh38.p7	11:118495765	ATGCTCAGTGGCAGG[A/G]GCGAGAGGAAAACAG	4297
rs782055111	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118465903	CTGTTAGGAGTTTTG[A/G]CTGTTTTTGTTTTGT	4297
rs782055143	snp	A/T			intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118519269	CTGTTTGCTCACCTG[A/T]AAATGAAGCTAGTAA	4297
rs782055593	snp	G/T	2.20179e-05	0.0033179	synonymous-codon	KMT2A	GRCh38.p7	11:118436800	TTCGTCTTCGTCATC[G/T]TCCTCAGCCTCTTCA	4297
rs782057036	snp	C/T	1.65405e-05	0.00287576	synonymous-codon	KMT2A	GRCh38.p7	11:118498438	CTGCACCAGCAACTA[C/T]CACTTCATGTGTTCC	4297
rs782057521	snp	A/C	1.65455e-05	0.00287619	missense, intron-variant	KMT2A	GRCh38.p7	11:118472589	TGTCTTCAGACTCCT[A/C]TCGATCTAGTAGCCC	4297
rs782057720	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118459879	TTTGGTAGAGACAGG[A/G]TTTCACCATGTCTCT	4297
rs782059730	snp	A/G	1.72761e-05	0.002939	synonymous-codon	KMT2A	GRCh38.p7	11:118491916	TACCAGCCATTTGCT[A/G]CGCTACCGGCAGGTA	4297
rs782060016	snp	A/G	0.000102283	0.00715058	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522221	GAGGCGGGGCCATCC[A/G]AAGCAACGCTGAAGG	4297
rs782062928	snp	C/G	5.07395e-05	0.00503659	intron-variant	KMT2A	GRCh38.p7	11:118501178	AGATGGGACTTGAGG[C/G]TGGGCACAGTGGCTC	4297
rs782063898	snp	C/T	1.70927e-05	0.00292336	intron-variant	KMT2A	GRCh38.p7	11:118495915	CACCAAAAGGAGAGT[C/T]GTCACCCATTTCCCT	4297
rs782063956	snp	C/G	1.65971e-05	0.00288067	missense, intron-variant	KMT2A	GRCh38.p7	11:118473691	TACCCCAGGCTCTCA[C/G]ACTGAAAGAGGGAGA	4297
rs782064249	snp	A/G	4.9423e-05	0.00497082	synonymous-codon	KMT2A	GRCh38.p7	11:118499374	AATCAGCTTGAGAAG[A/G]AAGTTTCTCAATGGC	4297
rs782065183	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118490703	AAGTTCATTAAGTAA[A/C]AAATAATATAGGAGA	4297
rs782065233	snp	C/T	1.74278e-05	0.00295188	intron-variant	KMT2A	GRCh38.p7	11:118507483	CACATTCAGTACATA[C/T]TTACTGGTGGTTTGT	4297
rs782066353	snp	A/C	1.65263e-05	0.00287452	missense	KMT2A	GRCh38.p7	11:118509987	AAAGTAATTTCAGCT[A/C]CCCACTGATGCTTTG	4297
rs782067101	snp	A/T	1.64735e-05	0.00286993	synonymous-codon	KMT2A	GRCh38.p7	11:118493134	CGAAGGACCTGATCC[A/T]CCAGTTCTTACTGAG	4297
rs782067204	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118441179	TTTGATAATTTTTGT[G/T]TTTTTTTTGAGTCAG	4297
rs782067347	snp	C/T	0.000151757	0.00870949	intron-variant	KMT2A	GRCh38.p7	11:118458224	AAGTAGCTGGGACTA[C/T]AGGCACCCACCACAC	4297
rs782067532	snp	A/G	1.64792e-05	0.00287042	missense, intron-variant	KMT2A	GRCh38.p7	11:118473957	AAAAAGCAACAGGGC[A/G]GAAGAAGTCTTCATC	4297
rs782068152	snp	A/G	1.64727e-05	0.00286986	synonymous-codon	KMT2A	GRCh38.p7	11:118505882	TACTAGCCACCTCAC[A/G]TCAGGGTCTGTGTCT	4297
rs782068215	snp	C/G	1.74503e-05	0.00295379	intron-variant	KMT2A	GRCh38.p7	11:118474329	AGGTACTCTTTTCCA[C/G]CTTGCCTATTAAAAC	4297
rs782068559	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118444048	TTCTTATTTTACAGC[A/G]TCAAGGTAATGGTAG	4297
rs782068838	snp	A/G	1.64762e-05	0.00287016	missense	KMT2A	GRCh38.p7	11:118502619	GATCTTGAATCAAGT[A/G]CCAAAGTAGTTGATC	4297
rs782068963	snp	C/T			missense	KMT2A	GRCh38.p7	11:118505445	ATCAGCAATCCTCCT[C/T]CAGGCCTGCTTATTG	4297
rs782070012	snp	A/G	1.64874e-05	0.00287113	synonymous-codon	KMT2A	GRCh38.p7	11:118505249	ACCCAGTGTGATGGA[A/G]ACAAATACTTCAGTA	4297
rs782070071	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118438682	TCCTGGGAAGAAGGG[C/G]AGGGAGGAGATCCCA	4297
rs782070742	snp	C/T	0.000115709	0.00760534	missense	KMT2A	GRCh38.p7	11:118481910	AAGAAGGGAATGTCT[C/T]GGCCCCTGGGCCTGA	4297
rs782071887	snp	C/G	1.64887e-05	0.00287125	synonymous-codon	KMT2A	GRCh38.p7	11:118499875	AATTCTAAATGATCT[C/G]TCCGACTGTGAAGAT	4297
rs782072736	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118493002	TTTAATAGAATTTAC[A/G]TGGACACCTTGGTTT	4297
rs782073017	snp	C/G	3.2994e-05	0.00406152	missense, intron-variant	KMT2A	GRCh38.p7	11:118473485	ACCCCCCCGTCTTCT[C/G]TCTCTTCCTCGTTAA	4297
rs782073705	snp	C/T			upstream-variant-2KB	KMT2A	GRCh38.p7	11:118435326	GATATTCATTCCCCT[C/T]CCTAACTCGCCTCCT	4297
rs782073757	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118500552	CAGCAGATTTGAAGC[-/A]AGTTACATTTCTCTT	4297
rs782074242	snp	A/C/T	3.31693e-05	0.00407231	missense, synonymous-codon	KMT2A	GRCh38.p7	11:118506578	GCACAAAGTTTCCCA[A/C/T]TTGCGGACCAGTTCT	4297
rs782074740	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118442539	TCGTGATTTTTGTGG[A/G]CTCTGAGGTTGTTGA	4297
rs782074982	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118510603	AATCTTACATGTTCT[C/T]CTCTCATAGCTTACA	4297
rs782075034	snp	A/G	1.69608e-05	0.00291206	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118472053	AAGGAAGGGGGTACA[A/G]ATTGTACGACGGAGA	4297
rs782075035	snp	C/G	0.00010538	0.00725801	synonymous-codon	KMT2A	GRCh38.p7	11:118502408	TTTAGGAAGTCCTAC[C/G]CCAACCACTCATGAA	4297
rs782075347	snp	A/G	1.65353e-05	0.00287531	missense	KMT2A	GRCh38.p7	11:118503217	AAGAAACTTTCAAAG[A/G]AAAGCATTCCAGTAA	4297
rs782076480	snp	C/G	1.6641e-05	0.00288448	intron-variant	KMT2A	GRCh38.p7	11:118468726	CTTTGGGATGTGTTT[C/G]TATGCACGTTTTTGC	4297
rs782077383	snp	A/G	0.000258231	0.01136	synonymous-codon	KMT2A	GRCh38.p7	11:118436701	GGCTGTGGCGGCCGC[A/G]GCGGCGGCGGCGGGA	4297
rs782077803	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118485571	TATAGATTAGTTACA[A/G]TCTTTCTTTCTGAGG	4297
rs782078199	snp	C/G	1.64866e-05	0.00287106	missense	KMT2A	GRCh38.p7	11:118504323	TCATTGGAGTCAAGC[C/G]GCAGAGTCCACACAA	4297
rs782078211	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118466540	AAAGAACTGGCTGGG[A/C]ACAGTGGCTCACGCC	4297
rs782078278	snp	C/T	1.65037e-05	0.00287256	missense	KMT2A	GRCh38.p7	11:118502848	TGAGTTCCAAGAGCT[C/T]AGAGGGATCTGCACA	4297
rs782078596	snp	A/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118515433	TAACAGAAAGTCCAG[A/T]GGTAGGGACAGACGT	4297
rs782078623	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118478580	CTAGTGGCTACCATA[A/T]CAGACTGTAGCTCTG	4297
rs782079486	snp	A/G	1.64738e-05	0.00286995	missense	KMT2A	GRCh38.p7	11:118505046	CAGAAGTATGTGCCC[A/G]ATTCTACTGATAGTC	4297
rs782079693	snp	C/T	1.64789e-05	0.0028704	missense	KMT2A	GRCh38.p7	11:118505527	GGACAGACCTCAGTA[C/T]CACAGTAGCCACTCC	4297
rs782080138	snp	A/G	5.77284e-05	0.00537223	missense	KMT2A	GRCh38.p7	11:118436924	TTTGGGGAGAGCGGC[A/G]GGGGAGGCGGCAGCG	4297
rs782080650	snp	C/T	0.000152616	0.00873411	intron-variant	KMT2A	GRCh38.p7	11:118484835	GTAATTGTAAAACTT[C/T]CCTAAGTGACCTTTC	4297
rs782081109	snp	C/T			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522331	TATACTCACATCAGA[C/T]ATGTGATCATAGTCC	4297
rs782081647	snp	A/T	1.74157e-05	0.00295085	synonymous-codon	KMT2A	GRCh38.p7	11:118482079	GAAAAAGCAGCCTCC[A/T]CCACCAGAATCAGGT	4297
rs782082584	snp	C/G	1.64787e-05	0.00287038	synonymous-codon	KMT2A	GRCh38.p7	11:118503455	GGCACCACGGAAACG[C/G]ACAGTCAAAGTGACA	4297
rs782085508	snp	C/G	1.65389e-05	0.00287562	missense	KMT2A	GRCh38.p7	11:118504122	AAAAGCAGCCAGATT[C/G]CAAAAAGAAATGGTA	4297
rs782086527	in-del	-/CCTCT			intron-variant	KMT2A	GRCh38.p7	11:118436994	GACCCTCTGCGGAGC[-/CCTCT]CCCCTCCCCTCCCCC	4297
rs782086591	snp	C/G	1.64784e-05	0.00287035	synonymous-codon, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519772	CCCTCACGGCTCAGC[C/G]AGGGCTGAAGTCCAC	4297
rs782086872	snp	A/G			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118523446	ACTCCTTAGGATGTG[A/G]TCAAAACAGCATCAA	4297
rs782087155	snp	C/T	1.65296e-05	0.00287481	synonymous-codon	KMT2A	GRCh38.p7	11:118503230	AGAAAAGCATTCCAG[C/T]AAATCTTTTTTGGAA	4297
rs782087392	snp	C/T	1.64784e-05	0.00287035	missense	KMT2A	GRCh38.p7	11:118503951	TTATACTATTACAAC[C/T]TCACTAGAACAGTGA	4297
rs782087590	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118467590	TTTAAGAGATGAACC[G/T]GCTAATTTGTCCTAA	4297
rs782087903	snp	C/T	1.65877e-05	0.00287986	intron-variant	KMT2A	GRCh38.p7	11:118491155	GTAAAAACACGGGTA[C/T]GTGAGCCAAAGCACT	4297
rs782087955	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118480469	TTATATAAAAATCAT[A/G]GTTCATTATATTTCC	4297
rs782087987	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118464206	AGCCAACACCATAGA[C/T]ATCTCAATTGGTTCA	4297
rs782088770	snp	A/G	1.64732e-05	0.0028699	missense, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522089	GAGGAACTCACTTAC[A/G]ACTATAAGTTCCCCA	4297
rs782089764	snp	A/C	1.64751e-05	0.00287007	missense	KMT2A	GRCh38.p7	11:118491792	AAAGTGTGGCCTACA[A/C]TTGTGTGAACTGTAC	4297
rs782089806	in-del	-/G	2.06354e-05	0.00321205	intron-variant	KMT2A	GRCh38.p7	11:118439168	GCAGCAAAAAAAAAA[-/G]AAAAAGAAAAAAAAG	4297
rs782090027	snp	A/G			missense	KMT2A	GRCh38.p7	11:118494364	AGCCAGAAATTAAAA[A/G]AGCCAACAGCATGGT	4297
rs782090440	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118487577	AACAAATAAAATACA[C/T]ATACACATTTTACCT	4297
rs782090480	snp	A/G	1.6534e-05	0.00287519	intron-variant	KMT2A	GRCh38.p7	11:118484143	ATGTGAAGGCAAATA[A/G]GGTGTGATTTTGTTC	4297
rs782091928	snp	A/G/T	3.33941e-05	0.00408609	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520758	CAAGACTCAAAACAT[A/G/T]ATTTCCTGAAAAAAA	4297
rs782092743	snp	A/G	4.96167e-05	0.00498055	synonymous-codon	KMT2A	GRCh38.p7	11:118501080	TCCAGTCGTAGAGCC[A/G]GATATCAACAGCACT	4297
rs782092804	snp	A/G	1.67609e-05	0.00289486	synonymous-codon	KMT2A	GRCh38.p7	11:118509190	TCCAGCAAATGAACA[A/G]GAAAGTGCAGGTATG	4297
rs782094382	snp	A/C	1.66446e-05	0.00288479	missense	KMT2A	GRCh38.p7	11:118474294	TAAGAGTCTTAAACA[A/C]ACCGACCAGCCCAAA	4297
rs782094920	snp	C/T	3.29462e-05	0.00405857	missense	KMT2A	GRCh38.p7	11:118496333	ACAATAGACAGTGTG[C/T]GTTATGTTTGACTTA	4297
rs782096084	snp	A/G	1.65488e-05	0.00287647	missense, intron-variant	KMT2A	GRCh38.p7	11:118472606	CGATCTAGTAGCCCC[A/G]GTGTTGATACCTCCA	4297
rs782096521	snp	C/T	1.65075e-05	0.00287289	missense, intron-variant	KMT2A	GRCh38.p7	11:118473822	AGAATAAGCGGGAGT[C/T]AAGGAAAGAGAAAAG	4297
rs782096692	snp	G/T			intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118511559	GAGAGGTTATGATCT[G/T]CCCACAGTCCTGCTT	4297
rs782097955	snp	A/C	0.0041526	0.0453768	missense	KMT2A	GRCh38.p7	11:118495777	AGGAGCGAGAGGAAA[A/C]CAGCCACACTGAGCA	4297
rs782098204	snp	G/T	1.66538e-05	0.00288559	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473286	AAGTGAGGCTCACTC[G/T]AGAATATTTGAGTCT	4297
rs782098738	in-del	-/G	0.000173021	0.00929949	intron-variant	KMT2A	GRCh38.p7	11:118510160	ATCAGCAGAAGCCCT[-/G]TTTCAGCTAGAGCTT	4297
rs782099821	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118476342	TGAATTTTGAGGGGA[A/T]TTTAAAATAGTAGTA	4297
rs782100291	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118506952	AATGATTATTCTTAT[C/T]TTGAGGGCAAAGCTC	4297
rs782101853	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118459812	CTTCCTCAGCCTCCC[A/G]AGTAGCTAGGATTAC	4297
rs782102967	snp	A/G			upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118525517	CCAGACTCCTTTGCC[A/G]GGACCCAGCCCGCCA	4297
rs782103460	snp	A/C	1.81955e-05	0.0030162	intron-variant	KMT2A	GRCh38.p7	11:118506690	GGTCTGTGGGATTTC[A/C]TGTTGTAAATTAGGG	4297
rs782103810	snp	C/T	1.66718e-05	0.00288715	intron-variant	KMT2A	GRCh38.p7	11:118500954	GCTTCTATCCTCTCC[C/T]TTATGATGATTTTCC	4297
rs782104438	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118442934	CCTTTACCTGGACCC[A/G]GATGGCTTCATTGAT	4297
rs782104513	snp	G/T	3.29468e-05	0.00405861	missense	KMT2A	GRCh38.p7	11:118498037	TGACGGATCACTAAA[G/T]AATGTGCATATGGCT	4297
rs782104581	snp	A/G	1.64893e-05	0.0028713	synonymous-codon	KMT2A	GRCh38.p7	11:118506140	ACTGGGGACATCACA[A/G]ACCCCCTCTACTGCT	4297
rs782104887	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118441148	TTATTTCAAAAGTCA[G/T]AGTCAAGTGAGACGA	4297
rs782106027	snp	A/G	1.72528e-05	0.00293703	intron-variant	KMT2A	GRCh38.p7	11:118501897	GACCTAAGAAGATCA[A/G]CCCAAAGACTAATTT	4297
rs782106243	snp	A/G	1.64743e-05	0.00287	missense	KMT2A	GRCh38.p7	11:118505557	CATCCTCTGGACTCA[A/G]GAAAAGACCCATATC	4297
rs782106779	snp	C/T	1.64762e-05	0.00287016	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118474165	CACTGTTAAACATTC[C/T]ACTTCCTCCATAGGC	4297
rs782106829	snp	A/T	1.64814e-05	0.00287061	missense	KMT2A	GRCh38.p7	11:118506006	TTAACCAACCCAAGG[A/T]TGCTTGGTACCCCAG	4297
rs782107284	snp	A/G	1.72988e-05	0.00294093	intron-variant	KMT2A	GRCh38.p7	11:118495933	CACCCATTTCCCTCT[A/G]GATGCAGATGATTGA	4297
rs782107354	snp	A/C	3.29462e-05	0.00405857	missense	KMT2A	GRCh38.p7	11:118506333	GATTCTGCTTCAGGG[A/C]CCCAGGTATCCAACT	4297
rs782109128	snp	A/C	1.64895e-05	0.00287132	missense	KMT2A	GRCh38.p7	11:118505387	TCATCACCAGCACTT[A/C]CATTCCTTCCCTGCA	4297
rs782109378	snp	A/G	0.00016478	0.0090754	missense	KMT2A	GRCh38.p7	11:118502512	CCTTATCACCCCAGC[A/G]GTCCAAACTCCGGAT	4297
rs782109994	snp	C/T	4.94703e-05	0.0049732	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473055	AGAGCCACAATACTT[C/T]TCCTCAGCAAAGTAT	4297
rs782110855	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118483594	TTCCTTGTTGCTTTT[A/C]CCTTCTTTGTGGCCC	4297
rs782111079	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118447265	GACTCCCTTAAGACA[C/T]GGGCCATTTCTAAGT	4297
rs782112254	snp	A/G	1.64746e-05	0.00287002	missense	KMT2A	GRCh38.p7	11:118502941	AACTGAATGTTAGTA[A/G]AATCGGCTCCTTTGC	4297
rs782112520	snp	C/G	2.21771e-05	0.00332988	missense	KMT2A	GRCh38.p7	11:118436787	CGTCCGCCTCGTCTT[C/G]GTCTTCGTCATCGTC	4297
rs782112729	snp	A/G			upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118526181	ATGGTAGAACAGTCC[A/G]TTCCTCGGATCAGAG	4297
rs782112874	snp	A/G	1.72704e-05	0.00293852	intron-variant	KMT2A	GRCh38.p7	11:118501196	GGCACAGTGGCTCAC[A/G]CCTGTAATCGCAGCA	4297
rs782113710	snp	G/T	0.000476304	0.0154248	missense	KMT2A	GRCh38.p7	11:118436594	GGGCGCCGGGGCCTA[G/T]GGGGCGCCCCGCGGC	4297
rs782113711	snp	A/G	1.64817e-05	0.00287064	missense	KMT2A	GRCh38.p7	11:118504551	GAAGGATTGGGTCTT[A/G]ACAGTAATCGTGAAA	4297
rs782113867	snp	A/G	3.29495e-05	0.00405877	missense	KMT2A	GRCh38.p7	11:118499385	GAAGGAAGTTTCTCA[A/G]TGGCTTGGAACCAGA	4297
rs782113912	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118476615	TTGATTAGAGGCCTT[G/T]TTTTGTGCTGCCAAT	4297
rs782115031	snp	A/G	3.29571e-05	0.00405924	missense	KMT2A	GRCh38.p7	11:118506207	TCCACTCAGACTACG[A/G]GCATAACAGCCGCTT	4297
rs782115318	snp	A/C	1.64909e-05	0.00287144	missense	KMT2A	GRCh38.p7	11:118503052	GAGACCAACACACAG[A/C]TTCTACCCAATCAGC	4297
rs782115705	snp	G/T	1.6486e-05	0.00287102	synonymous-codon	KMT2A	GRCh38.p7	11:118502645	TGATCATGTCTTAGG[G/T]CCACTGAATTCAAGT	4297
rs782117646	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118438189	GGATTATCAAGCAAA[C/G]TTATTCCTTAGAAAG	4297
rs782118554	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118499706	AATCACTTGAACCCC[A/G]GAGGCAGAGGCTGCA	4297
rs782119861	snp	C/T			synonymous-codon, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521926	TATGTTCCGAATTGA[C/T]GACTCAGAGGTAGTG	4297
rs782119903	snp	A/G	3.67999e-05	0.00428936	intron-variant	KMT2A	GRCh38.p7	11:118482105	CAGGTGAGTGAGGAG[A/G]GCAAGAAGGAATTGC	4297
rs782120345	snp	A/G	3.29625e-05	0.00405958	missense	KMT2A	GRCh38.p7	11:118484256	CTCTCTCCAATGGCA[A/G]TAGTTCTAAGCAAAA	4297
rs782120374	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118494910	GTGTGGTTTTGAGGA[C/T]TACATTTAATGTTTG	4297
rs782121049	snp	A/G	1.6492e-05	0.00287154	intron-variant	KMT2A	GRCh38.p7	11:118477963	TGCCACATTTCTTTA[A/G]CAGACAAGTCATCAA	4297
rs782121890	snp	A/G	1.64849e-05	0.00287092	synonymous-codon	KMT2A	GRCh38.p7	11:118504301	TTCCTTGGAAGCTCA[A/G]CTCAGCTCATTGGAG	4297
rs782122011	snp	A/G			synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118472800	GACGAAAAAATTATC[A/G]ACTCTACAAAGTGCC	4297
rs782123293	snp	C/T	3.31159e-05	0.00406901	intron-variant	KMT2A	GRCh38.p7	11:118484855	AGTGACCTTTCTCTC[C/T]CCACAGGAGGATTGT	4297
rs782124549	snp	A/G	4.94352e-05	0.00497143	missense	KMT2A	GRCh38.p7	11:118501798	AGGTCCCCAGGATTC[A/G]AACACCCAGTTATTC	4297
rs782124589	snp	A/C/T			intron-variant	KMT2A	GRCh38.p7	11:118486053	GCCCCACTGCACTCC[A/C/T]GCCTGGGCGACAGAG	4297
rs782124830	snp	A/G	1.64746e-05	0.00287002	synonymous-codon	KMT2A	GRCh38.p7	11:118488640	CCAAGTCTGTTGTGA[A/G]CCCTTCCACAAGTTT	4297
rs782125310	snp	A/G	1.66452e-05	0.00288484	missense	KMT2A	GRCh38.p7	11:118491897	CTTTGTTGAATTCTC[A/G]GACTACCAGCCATTT	4297
rs782126366	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118460308	TTTTTCTTTTTTCTG[A/C]GATAGGGACTTGCTC	4297
rs782126576	snp	A/G	8.48025e-05	0.00651107	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118472074	ACGACGGAGAGGAAG[A/G]CCTCCATCAACAGAA	4297
rs782127986	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118458340	GCCATCCTCCCTCCT[C/T]GGCCTCCCATTGTTA	4297
rs782128844	snp	C/T	3.29527e-05	0.00405898	missense	KMT2A	GRCh38.p7	11:118505676	TTGATTAACTTCACA[C/T]CCTCCCAGCTTCCTA	4297
rs782129160	snp	A/G	0.000313933	0.0125247	missense, intron-variant	KMT2A	GRCh38.p7	11:118472688	ATACCCCTGAAGTTC[A/G]TCCTCCACTGCCCAT	4297
rs782129370	snp	C/T	1.65644e-05	0.00287783	intron-variant	KMT2A	GRCh38.p7	11:118480151	ATTTAATTTGTTTCA[C/T]GGTTTATTCGTTGTT	4297
rs782129680	snp	C/T	1.64795e-05	0.00287045	missense	KMT2A	GRCh38.p7	11:118503447	GAATTACAGGCACCA[C/T]GGAAACGCACAGTCA	4297
rs782129810	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118489992	GATGTCAGTATGACA[A/G]TCTTTTTGCCTCATT	4297
rs782130634	snp	A/G	1.6501e-05	0.00287232	synonymous-codon	KMT2A	GRCh38.p7	11:118502852	TTCCAAGAGCTCAGA[A/G]GGATCTGCACATAAT	4297
rs782130840	snp	C/G	1.64738e-05	0.00286995	missense	KMT2A	GRCh38.p7	11:118505027	AACTGTTCCCATCCA[C/G]AACCAGAAGTATGTG	4297
rs782131131	snp	A/C			intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118511870	GTAGGGATTCTAAGC[A/C]GTGCTTGTGCACATC	4297
rs782131244	snp	A/G	1.69275e-05	0.0029092	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520923	AATTACAGAAAACGA[A/G]TGCAGTTTTTCAAAA	4297
rs782131280	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118453723	GCCAGGCTATATTCT[C/G]AGCACTTCACATGAA	4297
rs782131351	snp	A/G	3.28003e-05	0.00404958	intron-variant	KMT2A	GRCh38.p7	11:118488513	AATTAAATATATGCC[A/G]GTGGACTACTAAAAC	4297
rs782131394	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118498551	AGCTTTAGTTGCTTT[-/A]AAAAAAAAAAAAAAG	4297
rs782131470	snp	C/G	1.73084e-05	0.00294175	intron-variant	KMT2A	GRCh38.p7	11:118507497	ATTTACTGGTGGTTT[C/G]TCTTGAAAAGATACA	4297
rs782131845	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118475190	CTTAGCCTTGAGCCA[G/T]GGAACAGGAAAGCTA	4297
rs782132538	snp	C/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118516899	ATCTTTGTTTTCCCA[C/T]TATCAACACAATATT	4297
rs782132678	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118468244	CTCTCTGGATCTCAA[A/G]TGTACAGAAATCACA	4297
rs782132712	snp	A/T	3.30584e-05	0.00406548	missense, splice-acceptor-variant	KMT2A	GRCh38.p7	11:118489793	ATATTTTCTTACAGC[A/T]GCTGCTGGAGTGTAA	4297
rs782134028	snp	A/G	1.697e-05	0.00291285	intron-variant	KMT2A	GRCh38.p7	11:118495904	TTTGAGTAAGCCACC[A/G]AAAGGAGAGTCGTCA	4297
rs782134872	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118480360	TCTCAGGGAGTAGAT[C/T]GTTGAAGCTAGGTAA	4297
rs782134894	snp	C/T	2.04059e-05	0.00319414	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520106	TAGAAACTGCTTTCC[C/T]TCTCCTCCAGCTGGT	4297
rs782136104	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118456793	TTTTCTTCAGATCAT[C/T]ATACCCTTTAGACAA	4297
rs782136369	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118496638	ACCCTTGATGTCTAG[C/T]AATTTCTAATGGAAG	4297
rs782137297	snp	A/G	6.60502e-05	0.00574637	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473097	TCTTATTCGCAAACC[A/G]ATATTTGATAATTTC	4297
rs782137818	snp	C/G	1.65364e-05	0.0028754	missense	KMT2A	GRCh38.p7	11:118504118	AAGGAAAAGCAGCCA[C/G]ATTCCAAAAAGAAAT	4297
rs782138472	snp	C/T			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118523287	GACTTAATTTTTAAA[C/T]GGTCAGTGTCCAGTT	4297
rs782140426	snp	C/T	1.64735e-05	0.00286993	missense	KMT2A	GRCh38.p7	11:118491253	ACTATGAGAGTAAGA[C/T]GATGCAATGTGGAAA	4297
rs782140495	snp	A/C	1.75813e-05	0.00296485	intron-variant	KMT2A	GRCh38.p7	11:118439005	TTTTTTTTGAAAGGC[A/C]AATTCTGTATTTTTT	4297
rs782141187	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118439221	CTGCTTATTTTCAAA[A/G]TTGAGACTTGCCTGG	4297
rs782141414	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118500953	TGCTTCTATCCTCTC[C/T]CTTATGATGATTTTC	4297
rs782141758	snp	A/G			intron-variant, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519577	ATGCTGTTTCCTGTT[A/G]ACTGCGCTCCTCACT	4297
rs782141865	snp	A/T	1.65693e-05	0.00287826	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118471867	AAAAATCAAAATAAC[A/T]CATGGAAAGGACATT	4297
rs782142171	snp	A/G/T	0.000131884	0.00811956	missense	KMT2A	GRCh38.p7	11:118510023	AGCAAGAACAAAAGC[A/G/T]GAAGGAAAGCATTAC	4297
rs782142232	snp	A/C	1.64751e-05	0.00287007	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473850	AAGGAAAAAGGGATC[A/C]GAAATTCAGAGTAGT	4297
rs782142241	snp	A/G	1.64754e-05	0.00287009	missense	KMT2A	GRCh38.p7	11:118496359	ACTTATGGTGATGAC[A/G]GTGCTAATGTAAGTA	4297
rs782143255	snp	G/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118513047	AGTTCAAGACCAGCC[G/T]GGGCTTCATACAGAG	4297
rs782143434	snp	C/G	1.64743e-05	0.00287	synonymous-codon, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519748	GGAGGCCAATGAACC[C/G]CCCTTGAACCCTCAC	4297
rs782144224	snp	C/T	1.64762e-05	0.00287016	synonymous-codon	KMT2A	GRCh38.p7	11:118506248	GGAAGCAGACGAACA[C/T]TATCAGCTTCAGCAT	4297
rs782145320	snp	A/C	1.64784e-05	0.00287035	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118472869	GCTGACTCCACCGCC[A/C]CCACTGCAGCCAGCC	4297
rs782145460	snp	A/G	1.64931e-05	0.00287163	missense	KMT2A	GRCh38.p7	11:118499846	TCAGGGTCTATGACA[A/G]TCGACTGCTTAGGAA	4297
rs782147840	snp	A/G	2.79263e-05	0.00373663	intron-variant	KMT2A	GRCh38.p7	11:118494448	TACCTATAAGTAATT[A/G]CCCTGTGAATACAAT	4297
rs782148609	snp	G/T	1.68635e-05	0.0029037	intron-variant	KMT2A	GRCh38.p7	11:118478224	GGTGTTTCACTCTGA[G/T]ATGTTGACCTCTCAA	4297
rs782149580	snp	G/T			missense	KMT2A	GRCh38.p7	11:118503337	TGGGCCAACGACCAT[G/T]TAACAATGTTTCTTC	4297
rs782149629	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118443981	AACATTCATACTGTT[G/T]TAGAGAGATCCACTT	4297
rs782150410	snp	A/G	1.65864e-05	0.00287974	missense, intron-variant	KMT2A	GRCh38.p7	11:118473684	CTTGGTTTACCCCAG[A/G]CTCTCAGACTGAAAG	4297
rs782150443	snp	C/T	1.64735e-05	0.00286993	missense	KMT2A	GRCh38.p7	11:118505067	ACTGATAGTCCTGGC[C/T]CGTCTCAGATTTCCA	4297
rs782151492	snp	C/G	1.65345e-05	0.00287524	missense	KMT2A	GRCh38.p7	11:118502798	AGACTTGGTGTCCAA[C/G]AGCTCCTCTTTAAAG	4297
rs782152021	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118450112	TTAATTTTCTACAGT[C/G]AATCAGTTAAGTGGG	4297
rs782152509	snp	C/T	6.65314e-05	0.00576726	intron-variant	KMT2A	GRCh38.p7	11:118488469	TACTGTACTTTTTTA[C/T]ATAGTCATTGCTTAA	4297
rs782153029	snp	A/C/G	3.30941e-05	0.0040677	missense	KMT2A	GRCh38.p7	11:118495834	CAGCTCCCAAACCCA[A/C/G]AGGTCCTGGAGAACC	4297
rs782153387	snp	C/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118515120	CAGAATCCCTGGGCT[C/T]GGAGCTGAGAAAGCT	4297
rs782153447	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118485812	ATATAGCTGGGCACG[C/G]TGGCTCACGCCTGTA	4297
rs782154797	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118454823	CAAAATATTCTTTTG[A/C]CTTTAAAAAAATGGT	4297
rs782154992	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118510452	TTGTGTGCCTTCACA[C/T]GTGCTTTCTCCTCTG	4297
rs782156703	snp	C/T	3.32154e-05	0.00407512	intron-variant	KMT2A	GRCh38.p7	11:118468896	TGTTTGTTAGGAGAT[C/T]GTGGCTTCCTCTTGC	4297
rs782157422	snp	G/T	3.29723e-05	0.00406018	missense	KMT2A	GRCh38.p7	11:118476828	AAGTGACTCATCAGA[G/T]ACCTCTGTGCGAGGA	4297
rs782158314	in-del	-/A	0.000195446	0.00988356	intron-variant	KMT2A	GRCh38.p7	11:118447691	TCAAAAGATGATTAT[-/A]ATGATTGGAAGTCAG	4297
rs782158657	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118476436	GGGTGGCTCAAGTGA[A/T]CCTCTTGTCCCAGCC	4297
rs782159152	snp	A/G	1.64776e-05	0.00287028	missense	KMT2A	GRCh38.p7	11:118505988	GTTCCAGGACACGTC[A/G]CCTTAACCAACCCAA	4297
rs782159203	snp	A/G	1.82261e-05	0.00301872	intron-variant	KMT2A	GRCh38.p7	11:118502378	ACAATAGCATTTATT[A/G]CTTTTTCTCTCTTGT	4297
rs782159541	snp	A/G	3.30633e-05	0.00406578	missense	KMT2A	GRCh38.p7	11:118504156	AAAATGGAACAGAGA[A/G]CTTAAAGATTGATAG	4297
rs782160804	snp	A/G	1.64738e-05	0.00286995	synonymous-codon	KMT2A	GRCh38.p7	11:118488661	CCACAAGTTTTGTTT[A/G]GAGGAGAACGAGCGC	4297
rs782160840	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118484365	GTCAAAGACTTTAAA[A/T]AAAGAAAATGCTACT	4297
rs782160865	snp	A/G	1.65334e-05	0.00287514	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519812	GTTCCCTTCTTTTCT[A/G]TCAGCAGTTTTGGGT	4297
rs782162747	snp	C/T	1.65029e-05	0.00287248	missense	KMT2A	GRCh38.p7	11:118503259	AACCTGGTCAGGTGA[C/T]AACTGGTGAGGAAGG	4297
rs782163929	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118442741	TCTTGAGATTTTCAG[A/G]AATTGTCTAGGCTTC	4297
rs782164421	snp	C/T	3.29506e-05	0.00405884	synonymous-codon	KMT2A	GRCh38.p7	11:118502954	TAAAATCGGCTCCTT[C/T]GCTGAACCCTCTTCA	4297
rs782164581	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118506793	GACTTTTTTTCTCTC[C/T]GAGTGGTGATTTATG	4297
rs782165681	snp	C/T	1.64765e-05	0.00287019	missense	KMT2A	GRCh38.p7	11:118502530	CCAAACTCCGGATAA[C/T]GTCTCCAATGAGAAC	4297
rs782166237	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118447175	GTTTTGTATGTTATC[C/T]TTAAAAAATTTAACC	4297
rs782166364	snp	A/C	1.65674e-05	0.00287809	missense, intron-variant	KMT2A	GRCh38.p7	11:118472328	AGAAAATTGAAAAAG[A/C]AGCAGCTCAGCTGCA	4297
rs782167026	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118478768	CATATGGAATTTTTT[C/T]TTTTAAGAGACAGGG	4297
rs782169177	snp	C/T	1.66258e-05	0.00288316	intron-variant	KMT2A	GRCh38.p7	11:118491149	AGGGCCGTAAAAACA[C/T]GGGTATGTGAGCCAA	4297
rs782169403	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118448808	GAAGCTGGATTGTTG[A/C]AGGAATTCTGCAATT	4297
rs782170406	snp	C/T	1.64996e-05	0.0028722	missense	KMT2A	GRCh38.p7	11:118505359	CTGCTAGCAAAGGAT[C/T]GCTACCCATGTCTCA	4297
rs782171210	snp	A/G	4.94279e-05	0.00497107	missense	KMT2A	GRCh38.p7	11:118505643	ATTGCCCCTTCTGAT[A/G]TGGTTTCTAATATGA	4297
rs782171502	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118438064	CCTTTTCCTAGGCCA[A/G]TCCTGGGGCTTGGAA	4297
rs782171611	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118487189	TTTCCGTCTTAATAC[A/C]GTGCTTTGCACCCAT	4297
rs782171684	snp	C/T	1.64776e-05	0.00287028	missense	KMT2A	GRCh38.p7	11:118503994	GAGAGGAACGACTGG[C/T]ATCCCATAATTTATT	4297
rs782171990	snp	A/T	1.65111e-05	0.0028732	missense	KMT2A	GRCh38.p7	11:118503085	ACTCCTCTCCAGATG[A/T]AGATACTGAAGTCAA	4297
rs782172505	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118440920	CAGAGTGGAGTGCAC[A/G]AAGCCTCCGAGTAGA	4297
rs782173052	snp	C/T	9.04118e-05	0.00672293	intron-variant	KMT2A	GRCh38.p7	11:118509108	AAGAACTAGCTGATA[C/T]TATATCTTACATTTG	4297
rs782173501	snp	A/G	5.04223e-05	0.00502082	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118471954	TTCTGCTACGTTTCA[A/G]CAAGCCACAAAGATT	4297
rs782174272	snp	A/G	6.60338e-05	0.00574566	missense	KMT2A	GRCh38.p7	11:118506079	AGAGCCTGGGGATTC[A/G]GGACCAGCCTGTGGC	4297
rs782174587	snp	A/C	1.65436e-05	0.00287602	missense	KMT2A	GRCh38.p7	11:118502769	TCTTCAGAAATGAAG[A/C]AGTCCAGTGCTTCAG	4297
rs782174887	snp	A/G	0.000159732	0.00893534	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118434940	GGTTTTCAGCACCAG[A/G]AGGCTGTGGACCTTC	4297
rs782175106	snp	C/T	1.64944e-05	0.00287175	synonymous-codon	KMT2A	GRCh38.p7	11:118504523	ATCTTCATCAGAACT[C/T]CTGAATCTTGGTGAA	4297
rs782175796	snp	A/T	0.000141133	0.00839921	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118434850	CTTGCCTGTGTCTCC[A/T]CCCTTTCATTGCTCC	4297
rs782176578	snp	A/G	1.64754e-05	0.00287009	missense	KMT2A	GRCh38.p7	11:118504953	GAGCAAGGTCATGGC[A/G]ACAATCAGGATTTAA	4297
rs782177007	snp	C/T	1.64768e-05	0.00287021	synonymous-codon	KMT2A	GRCh38.p7	11:118502570	TTACTCTAGGAATAA[C/T]GTTTCCTCAGTCTCC	4297
rs782178264	snp	A/C	1.64765e-05	0.00287019	missense	KMT2A	GRCh38.p7	11:118506412	AGGCTTTATCCTCAG[A/C]TGTGCAAGCCAGCCC	4297
rs782179214	snp	C/T	1.64781e-05	0.00287033	synonymous-codon	KMT2A	GRCh38.p7	11:118478157	TACTAATTGCTTAGA[C/T]AAGCCCAAGTTTGGT	4297
rs782181274	snp	A/G	0.000115698	0.00760496	missense	KMT2A	GRCh38.p7	11:118503147	TCATCCATTATCAAC[A/G]AACATATGGGATCTA	4297
rs782181355	snp	C/T	1.68687e-05	0.00290414	intron-variant	KMT2A	GRCh38.p7	11:118501869	GCAGGTAAAAGACTT[C/T]ATTGACCTACTTGAC	4297
rs782182398	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118507788	AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT	4297
rs782182788	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118495953	CAGATGATTGACTTC[A/G]TGAATCCAATTCACT	4297
rs782183780	snp	A/C	1.65258e-05	0.00287448	synonymous-codon	KMT2A	GRCh38.p7	11:118504103	TGTCACAGCCACAAC[A/C]AGGAAAAGCAGCCAG	4297
rs782184234	snp	C/G	3.30699e-05	0.00406618	missense, intron-variant	KMT2A	GRCh38.p7	11:118473626	AAGCAGACTAGTGCT[C/G]CGGCAGAGCCATTTT	4297
rs782184802	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512600	TTGCCACAAATATTC[A/G]TGTTCAAGTTATTGT	4297
rs782184805	snp	A/C	3.29538e-05	0.00405904	synonymous-codon	KMT2A	GRCh38.p7	11:118504727	GAGTCCCACTGTCCC[A/C]AGCCAGAATCCCAGT	4297
rs782185843	snp	C/G	1.648e-05	0.0028705	synonymous-codon	KMT2A	GRCh38.p7	11:118502498	TCACAGTACCTCTTC[C/G]TTATCACCCCAGCGG	4297
rs782187139	snp	A/C/T	5.03808e-05	0.00501875	intron-variant	KMT2A	GRCh38.p7	11:118489922	CTCTTTTATAGAGAA[A/C/T]CACCATGTGACTATT	4297
rs782187838	snp	C/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118518508	GAGGCTGGCTGGGTG[C/T]TGTGGCTCACACCTG	4297
rs782187884	snp	C/T	3.29614e-05	0.00405951	intron-variant	KMT2A	GRCh38.p7	11:118488600	ACTTCTATCTTCCCA[C/T]GTTCTTACTATAGTT	4297
rs782188358	snp	C/G	1.64735e-05	0.00286993	missense	KMT2A	GRCh38.p7	11:118505950	CCATGCAAACTACCA[C/G]AACCCCTACAAGTAG	4297
rs782188541	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118439159	AAAAGATACAGCAGC[-/A]AAAAAAAAAAAAAAG	4297
rs782188552	snp	C/T	1.6473e-05	0.00286988	missense, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519722	TACAAATTCCGTTTC[C/T]ACAAGCCAGAGGAGG	4297
rs782188607	snp	C/T			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118524504	AGCCCAGCACTGTGG[C/T]CAGGATGGCAGAGAC	4297
rs782189523	snp	A/G	1.65677e-05	0.00287812	synonymous-codon	KMT2A	GRCh38.p7	11:118474273	GCTCTGCAAGATTGA[A/G]AAGAGTAAGAGTCTT	4297
rs782189997	snp	C/T	1.64958e-05	0.00287187	synonymous-codon	KMT2A	GRCh38.p7	11:118505285	ACCCATGGGAGGTGG[C/T]CTCACCCTTACCACA	4297
rs782191019	snp	C/G	5.59534e-05	0.00528901	missense	KMT2A	GRCh38.p7	11:118436750	CCAGGGGGAGCGGCC[C/G]CCGCCTCAGCAGCCT	4297
rs782192447	snp	A/G	1.6473e-05	0.00286988	missense, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522014	TGCTATTCTCGGGTC[A/G]TCAATATTGATGGGC	4297
rs782192738	snp	C/T	1.65018e-05	0.00287239	intron-variant, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512050	GGAGGTGTTATTCCA[C/T]TCCTGTCTCAGAATA	4297
rs782192767	snp	C/T	1.681e-05	0.00289909	intron-variant	KMT2A	GRCh38.p7	11:118491700	CTTCTTCCTCTCTCT[C/T]ATTCTTCAGAGGACC	4297
rs782194780	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118449725	TTTATGGAGAGATAA[C/T]CCTGTTTACCTTTAG	4297
rs782195145	snp	C/T	3.29979e-05	0.00406175	intron-variant	KMT2A	GRCh38.p7	11:118468848	GGTCTCCTTCAGGTA[C/T]GGCCAATTAAGTGCA	4297
rs782196437	snp	C/T	1.66671e-05	0.00288674	intron-variant	KMT2A	GRCh38.p7	11:118489776	CTTATCTTTTTGCCA[C/T]TATATTTTCTTACAG	4297
rs782197460	in-del	-/T			intron-variant	KMT2A	GRCh38.p7	11:118444893	AAGTTTTTGAACCTC[-/T]TCCATACCTCTGTTT	4297
rs782197542	snp	C/T	1.65296e-05	0.00287481	missense, intron-variant	KMT2A	GRCh38.p7	11:118472510	ACACCGAATAGTAGA[C/T]TCAGTGCCCCGTCCT	4297
rs782198212	in-del	-/T			intron-variant	KMT2A	GRCh38.p7	11:118463072	TATAAAAATGACTCA[-/T]TTAGGTTGTTAATAA	4297
rs782198350	snp	C/T			synonymous-codon	KMT2A	GRCh38.p7	11:118484203	ACCACCTCCGGTCAA[C/T]AAGCAGGAGAATGCA	4297
rs782199067	snp	C/G	1.64806e-05	0.00287054	missense	KMT2A	GRCh38.p7	11:118484243	AACATCCTCAGCACT[C/G]TCTCCAATGGCAATA	4297
rs782199290	snp	A/G	1.648e-05	0.0028705	synonymous-codon	KMT2A	GRCh38.p7	11:118503890	GAGATCAGCTGAAGG[A/G]CAGGTGGATGGGGCC	4297
rs782199472	snp	A/G	6.59446e-05	0.00574177	missense	KMT2A	GRCh38.p7	11:118503037	GGCAAAGGAATGATC[A/G]AGACCAACACACAGA	4297
rs782199640	snp	A/G			missense, intron-variant	KMT2A	GRCh38.p7	11:118474039	TGTCAAAACCAAAAT[A/G]CTTATAAAGAAAGGG	4297
rs782200100	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118439169	GCAGCAAAAAAAAAA[A/G]AAAAGAAAAAAAAGA	4297
rs782201002	snp	C/T	3.31928e-05	0.00407373	synonymous-codon	KMT2A	GRCh38.p7	11:118491892	GACAGCTTTGTTGAA[C/T]TCTCGGACTACCAGC	4297
rs782201274	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118499446	GCCTTGGTTATTGGG[A/G]AAGGCTGTATATATC	4297
rs782201855	snp	G/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118515007	CTCCTGAGCTTGTGA[G/T]CTGCCCACCTCGGCC	4297
rs782203458	snp	A/T	1.64743e-05	0.00287	missense, intron-variant	KMT2A	GRCh38.p7	11:118473919	GGTTGTTGGTGAAGA[A/T]GTTGCCACTTCATCT	4297
rs782203646	snp	A/G	1.65842e-05	0.00287955	intron-variant	KMT2A	GRCh38.p7	11:118497909	CATTATATTCTTTAG[A/G]AAAAAAGAAATCTCT	4297
rs782203750	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118447059	GCTTATTATTCGTCT[C/G]CCATGGTTCAACTCA	4297
rs782204025	snp	A/G	1.64781e-05	0.00287033	synonymous-codon	KMT2A	GRCh38.p7	11:118503560	GCAAATAGAGTCAAC[A/G]TCTCCCACAGAACCA	4297
rs782204033	snp	A/G	3.36412e-05	0.00410115	missense, intron-variant	KMT2A	GRCh38.p7	11:118472210	ACAGTTGTCAGACAA[A/G]GCCCTCGAAGGATTA	4297
rs782204370	snp	C/T	1.78854e-05	0.00299038	intron-variant	KMT2A	GRCh38.p7	11:118495658	CAGTTCTAGGTATAC[C/T]GTAGGAGTTCAATAA	4297
rs782206199	snp	G/T	5.05659e-05	0.00502796	intron-variant	KMT2A	GRCh38.p7	11:118476766	GTTATAATTTCAACA[G/T]GTATGGTTGTTATTG	4297
rs782206792	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118454451	CAAGGTCTTTATATG[A/T]CTGACTTTTTCTCAT	4297
rs782206846	snp	C/G	1.64936e-05	0.00287168	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473460	TAGTAGTTCTGAGCT[C/G]TCACCTCTCACCCCC	4297
rs782207243	snp	C/T	2.00656e-05	0.0031674	synonymous-codon	KMT2A	GRCh38.p7	11:118436539	CTGTCGGTGGCGCTT[C/T]CCCGCCCGACCCGGG	4297
rs782207980	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118509529	ACTAAAGAAAACTAA[G/T]AACCATTTTTATTAG	4297
rs782209629	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118511130	AATTTCAGGAAACAT[A/G]ATGTGATAAGCTCTC	4297
rs782210632	snp	A/G	1.6534e-05	0.00287519	missense	KMT2A	GRCh38.p7	11:118507572	GATACAGCTAGCGTG[A/G]AGCAGTCCTCCCAGA	4297
rs782210790	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118440624	CTGATCATAACATAG[C/T]AAACTTTAATTAGAT	4297
rs782210802	snp	A/G			synonymous-codon	KMT2A	GRCh38.p7	11:118506623	TCCAGACCAAGAAAC[A/G]ACATCCCTGACCTCA	4297
rs782211560	snp	C/T	1.64887e-05	0.00287125	synonymous-codon	KMT2A	GRCh38.p7	11:118502483	CATTGGCTCCAGGCG[C/T]CACAGTACCTCTTCC	4297
rs782211630	snp	A/T	0.000152958	0.0087439	intron-variant	KMT2A	GRCh38.p7	11:118498336	TAAAACATATGAAAG[A/T]CTGAATAGGACTCTG	4297
rs782211693	snp	C/T	1.64732e-05	0.0028699	missense	KMT2A	GRCh38.p7	11:118506301	AAACTGGGATTCATT[C/T]TTCCCAGCGTGATCT	4297
rs782212238	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118459359	GGTGTGAGCCACCAT[G/T]CCAGGCCCTGATTTT	4297
rs782212726	snp	A/C	1.65688e-05	0.00287821	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118471823	AGTATAGAAAAGAAG[A/C]GAGGAAGACCTCCCA	4297
rs782213033	snp	A/G	1.6537e-05	0.00287545	missense, intron-variant	KMT2A	GRCh38.p7	11:118472672	CCTGAGGAGCGGAGC[A/G]ATACCCCTGAAGTTC	4297
rs782213495	snp	C/G	1.64999e-05	0.00287222	missense	KMT2A	GRCh38.p7	11:118505326	CAAGCTTGCCAACTT[C/G]TCAATCTTTGTTCCC	4297
rs782215946	snp	A/C/G	5.01931e-05	0.00500944	missense, intron-variant	KMT2A	GRCh38.p7	11:118473759	GAGATGCTGACAAGA[A/C/G]CGTGGAGAAGGACAA	4297
rs782215977	snp	A/G	1.76993e-05	0.00297478	intron-variant	KMT2A	GRCh38.p7	11:118481702	AGATGATGTTGTTGT[A/G]TTTTTCCCTCAGCTG	4297
rs782216478	snp	A/G			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522736	ATTCCTAGCACCTCC[A/G]GTGTCAAAAGGCTGT	4297
rs782218480	snp	A/G	1.6473e-05	0.00286988	missense	KMT2A	GRCh38.p7	11:118505823	CCACAGAGTGTGGGA[A/G]GAACTGCTGCCACAG	4297
rs782218555	in-del	-/G	1.83998e-05	0.00303308	intron-variant	KMT2A	GRCh38.p7	11:118494279	TAACATTTTGTTTTT[-/G]GTATACAGTTGGAGT	4297
rs782218911	snp	C/T	1.65323e-05	0.00287505	missense	KMT2A	GRCh38.p7	11:118478183	TTGGTGGTCGCAATA[C/T]AAAGAAGCAGTGCTG	4297
rs782219735	snp	C/T	0.000197664	0.00993947	synonymous-codon	KMT2A	GRCh38.p7	11:118499344	TTTCAGAAGAGTGTT[C/T]GTGGACTTTGAAGGA	4297
rs782219744	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118452921	GCAGGCGTGAGCCAC[C/T]GTGCCTGGCGGAAGT	4297
rs782220474	snp	C/G	3.30518e-05	0.00406507	missense	KMT2A	GRCh38.p7	11:118481890	GCCCGTCGAGGAAAA[C/G]AGTGAAGAAGGGAAT	4297
rs782220511	snp	A/G	0.000155171	0.0088069	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118434915	AATGTTTCGCCAGTG[A/G]AGGGACGTAGGTTTT	4297
rs782220782	snp	C/G	1.64765e-05	0.00287019	synonymous-codon	KMT2A	GRCh38.p7	11:118502996	TTCTAAAGAGGCCCT[C/G]TCCTTCCCACACCTC	4297
rs782220808	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118474813	GAGCAATAGATAATA[C/T]GTTTTTGCAGAATAC	4297
rs782221510	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118457461	ATTTTTTAGTAGAGA[C/G]AGGGTTTCACCATGT	4297
rs782222821	snp	A/C	1.64846e-05	0.0028709	missense	KMT2A	GRCh38.p7	11:118504429	GTGATGACTGTGGGA[A/C]TATCCTGCCTTCAGA	4297
rs782224592	snp	A/T	1.6476e-05	0.00287014	synonymous-codon	KMT2A	GRCh38.p7	11:118503596	AGCCTCTGAAAATCC[A/T]GGAGATGGTCCAGTG	4297
rs782224867	snp	A/C	1.64781e-05	0.00287033	missense	KMT2A	GRCh38.p7	11:118484208	CTCCGGTCAATAAGC[A/C]GGAGAATGCAGGCAC	4297
rs782224958	snp	A/G			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118523048	CCAGGTGGGGAAGTG[A/G]ACAGGAGCCATTGGT	4297
rs782226053	snp	A/G	1.64754e-05	0.00287009	missense, intron-variant	KMT2A	GRCh38.p7	11:118474094	TTGGACCTCGGCCCA[A/G]CTGCCCCATCCCTGG	4297
rs782226185	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118497192	TATTTTTAGTAGAGA[C/T]GGAGTTTCTCCATGT	4297
rs782226640	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118486879	GGCAACTAAGCAAGA[A/C]CCTGTCTCAAAAAAA	4297
rs782226750	snp	C/T	4.94262e-05	0.00497098	missense	KMT2A	GRCh38.p7	11:118501726	TAAGTCCTCCATCAC[C/T]AGACCGACCTCCTCA	4297
rs782227542	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118443439	CAGGGGAAGCCAACC[A/G]TGAGACTGTAGCTGC	4297
rs782227605	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118479867	GAGTAGGACTGATGC[A/G]ACTACAAGAAATACT	4297
rs782228102	snp	C/T	3.35255e-05	0.0040941	synonymous-codon	KMT2A	GRCh38.p7	11:118482040	AAGAAAAGAAGTTCC[C/T]AAAACCACTCCTAGT	4297
rs782228317	snp	C/G	1.6476e-05	0.00287014	missense	KMT2A	GRCh38.p7	11:118505469	CTTATTGGGGTTCAG[C/G]CTCCTCCGGATCCCC	4297
rs782228523	snp	G/T	1.64776e-05	0.00287028	synonymous-codon	KMT2A	GRCh38.p7	11:118505183	TGTTCTCCAAACTCT[G/T]CCAAATGGAGTGACC	4297
rs782228819	snp	A/G	3.29533e-05	0.00405901	missense	KMT2A	GRCh38.p7	11:118506526	AACCAAAAACCAAAC[A/G]GTTTCAGCTGCCTCT	4297
rs782228843	snp	C/T	2.7436e-05	0.00370368	missense	KMT2A	GRCh38.p7	11:118436841	TGCTCCGGGTGGGCC[C/T]GGGCTTCGACGCGGC	4297
rs782229111	snp	A/G	3.29489e-05	0.00405874	missense	KMT2A	GRCh38.p7	11:118491831	ACCCTGCAGAGTGGC[A/G]ACTGGCCCTTGAAAA	4297
rs782230027	snp	A/C/T	1.658e-05	0.00287919	synonymous-codon	KMT2A	GRCh38.p7	11:118481995	GCCAGCACTGGTCAT[A/C/T]CCGCCTCAGCCACCT	4297
rs782230850	snp	A/C	1.64917e-05	0.00287151	synonymous-codon	KMT2A	GRCh38.p7	11:118504220	TAAGAGTTCTGTTGG[A/C]CACAAAAATGAGCCA	4297
rs782231421	snp	C/T	1.6797e-05	0.00289797	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522202	CCCAGTGTTGGAGTG[C/T]AAGGAGGCGGGGCCA	4297
rs782233076	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118502118	ATTAGCCAGGTGTGG[C/T]GGTGCATGCCTGTAA	4297
rs782233787	snp	A/G	0.0010537	0.022929	missense	KMT2A	GRCh38.p7	11:118436730	GAAGCAGCGGGGCTG[A/G]GGTTCCAGGGGGAGC	4297
rs782234076	snp	A/G	1.66779e-05	0.00288768	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118472251	GATTATTCCTTCTTC[A/G]AAAAGGACAGATGCA	4297
rs782234708	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118489437	GTCTTCCAGTTAAGA[C/T]TTTGTATCTATATTA	4297
rs782235007	snp	C/G	8.25307e-05	0.00642328	missense	KMT2A	GRCh38.p7	11:118506072	AGCCAGCAGAGCCTG[C/G]GGATTCAGGACCAGC	4297
rs782235146	snp	A/C	3.30836e-05	0.00406702	missense	KMT2A	GRCh38.p7	11:118502779	TGAAGCAGTCCAGTG[A/C]TTCAGACTTGGTGTC	4297
rs782236782	snp	C/T	1.65266e-05	0.00287455	intron-variant	KMT2A	GRCh38.p7	11:118491970	GAGCTTGTTCTTAGG[C/T]AGTCTTTACCTAGTG	4297
rs782236871	snp	A/G	1.64885e-05	0.00287123	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118472788	TGGATCTAGAACGAC[A/G]AAAAAATTATCAACT	4297
rs782237038	snp	A/C	1.64732e-05	0.0028699	missense	KMT2A	GRCh38.p7	11:118504674	CAGTTTGAGTTGCCT[A/C]TAGAGCTACCATCTG	4297
rs782238174	snp	A/G	1.65026e-05	0.00287246	missense, intron-variant	KMT2A	GRCh38.p7	11:118473587	CAGTCTGGGGAATCT[A/G]CAGAGAAAAATCAGA	4297
rs782238472	snp	C/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118514924	AGGCGTGAGCCACCA[C/T]GCCCGGCCTAATTTT	4297
rs782238661	snp	C/T	3.29576e-05	0.00405928	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118474063	GAAAGGGAGAGGAAA[C/T]CTGGAAAAAACCAAC	4297
rs782240356	snp	C/T	1.85482e-05	0.00304529	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520077	TCGGTAAGTCTTGAG[C/T]GGGGAGCAGTCATTA	4297
rs782241971	snp	C/T	3.30502e-05	0.00406497	missense	KMT2A	GRCh38.p7	11:118504090	AGAGTGATACTAGTG[C/T]CACAGCCACAACAAG	4297
rs782242103	snp	C/G	1.71737e-05	0.00293028	splice-acceptor-variant	KMT2A	GRCh38.p7	11:118509947	ATTTTCTCCCTATTA[C/G]AACCTAAAACAGTGG	4297
rs782242466	snp	C/G	1.64827e-05	0.00287073	synonymous-codon	KMT2A	GRCh38.p7	11:118503818	CTATGGAGTAAGATC[C/G]TATGGTGAAGAAGAC	4297
rs782243132	snp	A/G	1.64846e-05	0.0028709	synonymous-codon, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521941	TGACTCAGAGGTAGT[A/G]GATGCCACCATGCAT	4297
rs782244678	snp	C/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118516626	GCCTGTCTTGCTCAC[C/T]TGTAAGTTCCTAAGG	4297
rs782245671	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118509705	CTATCAGATCGTCAT[A/C]CTAGAAATTCTACCA	4297
rs782247010	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118460640	TGAATATGAATTACA[C/T]ATAGTATTTTATCCT	4297
rs782247800	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118471466	AATGTTCTTTCAGGT[A/G]GAATGTTATTTGCTG	4297
rs782249194	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521804	GAAACTTTCTCAGCC[A/G]CTATAGGTAACATCA	4297
rs782249940	snp	A/G	1.65195e-05	0.00287393	synonymous-codon	KMT2A	GRCh38.p7	11:118506569	TGGCAAGAAGCACAA[A/G]GTTTCCCATTTGCGG	4297
rs782251728	snp	C/T	1.6473e-05	0.00286988	synonymous-codon, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519709	GCACTGTCGAAATTA[C/T]AAATTCCGTTTCCAC	4297
rs782251942	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118456580	CCTGACCTCATGATT[A/C]GCCCACCTTGGCCTC	4297
rs782253408	snp	A/T	1.8051e-05	0.0030042	intron-variant	KMT2A	GRCh38.p7	11:118490298	AGGTTGTACTTGGTG[A/T]TCTGGAGGTGAACTA	4297
rs782253584	snp	A/C	6.58924e-05	0.0057395	synonymous-codon, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521322	GGTCTTTTCTGTAAG[A/C]GAAACATTGATGCAG	4297
rs782253798	snp	C/G	6.76739e-05	0.00581656	missense	KMT2A	GRCh38.p7	11:118494324	GTGAAGATCATTCAA[C/G]CAGCCATTAATTCAG	4297
rs782254170	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118469242	TGGGAAGTAGGTTTC[C/T]ACAGAATTACTGGGA	4297
rs782254286	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118451918	CAGAACTAATGTTAA[C/T]AGAATTGTCCTTGGG	4297
rs782255667	snp	C/T	1.64743e-05	0.00287	synonymous-codon	KMT2A	GRCh38.p7	11:118506431	GCAAGCCAGCCCCAC[C/T]TCTCCTGGGGGTTCT	4297
rs782256145	snp	A/C	1.6492e-05	0.00287154	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473425	CCTTCTCACTCCATG[A/C]GGACAAGAAGTGGAA	4297
rs782256438	snp	A/C	3.29468e-05	0.00405861	synonymous-codon	KMT2A	GRCh38.p7	11:118497962	TTTACTATATATTGG[A/C]CAAAATGAGTGGACA	4297
rs782257059	snp	C/T	1.64727e-05	0.00286986	synonymous-codon	KMT2A	GRCh38.p7	11:118478097	TCGATCGAGGCGGTG[C/T]GGGCAGTGTCCCGGC	4297
rs782257694	snp	A/G	1.65037e-05	0.00287256	missense	KMT2A	GRCh38.p7	11:118506090	ATTCAGGACCAGCCT[A/G]TGGCTTTACCGCCAA	4297
rs782258040	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118454225	TCTGTGTCTCCCCAC[A/C]CTGCTAGGATAAATC	4297
rs782258416	snp	C/T	1.65798e-05	0.00287917	intron-variant	KMT2A	GRCh38.p7	11:118499793	AAAAAAATAAAATGA[C/T]GCTCATAATCTTCTC	4297
rs782258934	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118496232	TAACTGGATCTCAAG[A/G]TATTGATGGGAGTCT	4297
rs782259353	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118452700	GTGCAGTGGCGCCAT[C/G]TCGGCTCACAGCAAC	4297
rs782260266	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118443674	GTTAGTTGGCAGTTT[C/T]GTGTGCAGTGTATGA	4297
rs782260289	snp	G/T	1.66131e-05	0.00288206	intron-variant	KMT2A	GRCh38.p7	11:118491733	ATCATGGTAGGTTTT[G/T]GTTTTCTTAGATGAG	4297
rs782260851	snp	A/G	1.64779e-05	0.00287031	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473007	TTTGCGAGAACCGAC[A/G]TTTAGGTGGACTTCT	4297
rs782261382	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118440401	CCATTTTTCTAAGGA[C/T]TCTCTCAGGTAATGT	4297
rs782261855	snp	C/T	1.64746e-05	0.00287002	synonymous-codon	KMT2A	GRCh38.p7	11:118505519	CAGCCAGAGGACAGA[C/T]CTCAGTACCACAGTA	4297
rs782261966	snp	C/T	4.94262e-05	0.00497098	missense, intron-variant	KMT2A	GRCh38.p7	11:118473935	GTTGCCACTTCATCT[C/T]CTGCCAAAAAAGCAA	4297
rs782262170	snp	C/T			upstream-variant-2KB	KMT2A	GRCh38.p7	11:118435204	GCCAACGCAAGTTCT[C/T]CCGACACAAACCCCT	4297
rs782262576	snp	A/G/T	3.36662e-05	0.0041027	intron-variant	KMT2A	GRCh38.p7	11:118501864	CTTCTGCAGGTAAAA[A/G/T]ACTTTATTGACCTAC	4297
rs782262729	snp	C/T	1.65157e-05	0.0028736	synonymous-codon	KMT2A	GRCh38.p7	11:118474238	AGGGTTGCCAGCCTC[C/T]TAAAAAAGGCCAAAG	4297
rs782263390	snp	C/G	1.67164e-05	0.00289101	missense, intron-variant	KMT2A	GRCh38.p7	11:118473775	CGTGGAGAAGGACAA[C/G]AGTAGAGAGAGAGAC	4297
rs782263597	snp	C/T	1.64819e-05	0.00287066	synonymous-codon	KMT2A	GRCh38.p7	11:118480219	GCCTTCCAAAGCCTA[C/T]CTGCAGAAGCAAGCT	4297
rs782263606	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118487370	AGAGAATAGCATGCT[G/T]CCTGCACTGCACTCC	4297
rs782263730	snp	G/T	1.65018e-05	0.00287239	intron-variant	KMT2A	GRCh38.p7	11:118499292	AACAGCTACCATGGG[G/T]TTTATTTAAGGTGGT	4297
rs782264066	snp	C/T	1.65433e-05	0.002876	missense, intron-variant	KMT2A	GRCh38.p7	11:118472565	CAGCTTCTCAGCACT[C/T]CTCTCAAATGTCTTC	4297
rs782264742	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118446885	AGCCTGTATTTCTAA[A/G]TTTTGAACCGTGTCT	4297
rs782265781	snp	C/G	3.3184e-05	0.00407319	synonymous-codon	KMT2A	GRCh38.p7	11:118498402	AAAGCCAGGAGCCAC[C/G]GTGGGTTGCTGTCTC	4297
rs782266039	snp	C/T	1.64741e-05	0.00286998	synonymous-codon	KMT2A	GRCh38.p7	11:118505966	AACCCCTACAAGTAG[C/T]GCGTCAGTTCCAGGA	4297
rs782266425	snp	C/G	1.64732e-05	0.0028699	missense	KMT2A	GRCh38.p7	11:118506291	CTTGCCAGCAAAACT[C/G]GGATTCATTCTTCCC	4297
rs782267324	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118488943	ATAACAACTATTTAC[A/C]TTGTATTAGGTATGA	4297
rs782267350	snp	C/T	1.658e-05	0.00287919	synonymous-codon	KMT2A	GRCh38.p7	11:118501104	CAGCACTGTTGAACA[C/T]GATGAAAACAGGACC	4297
rs782267863	snp	A/G	3.29592e-05	0.00405938	missense	KMT2A	GRCh38.p7	11:118502895	GGAATTCCTAAACTG[A/G]CCCCACAGGTTCATA	4297
rs782268376	snp	C/T	1.65277e-05	0.00287464	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118472494	TGCCCGATTAGAGTC[C/T]ACACCGAATAGTAGA	4297
rs782268821	snp	C/T	4.96726e-05	0.00498335	intron-variant	KMT2A	GRCh38.p7	11:118499953	GAGCAGCCCCACAAC[C/T]TGAACACACTGAAGC	4297
rs782269172	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512402	TAGCCTTTTGTGACC[A/G]TCTTCTTTCACTCAA	4297
rs782269485	snp	A/C	1.6473e-05	0.00286988	missense	KMT2A	GRCh38.p7	11:118505814	CCCCTGTTACCACAG[A/C]GTGTGGGAGGAACTG	4297
rs782269735	snp	C/T	1.64817e-05	0.00287064	synonymous-codon	KMT2A	GRCh38.p7	11:118504409	AGATTCAGACAATAA[C/T]AACAGTGATGACTGT	4297
rs782270340	snp	C/G	8.24831e-05	0.00642143	synonymous-codon	KMT2A	GRCh38.p7	11:118505297	TGGTCTCACCCTTAC[C/G]ACAGGACTAAATCCA	4297
rs782270743	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118500466	CTTACTCTGTATTCC[C/T]ATTCCTATGACACAG	4297
rs782270841	snp	A/C/T	3.29708e-05	0.00406011	missense	KMT2A	GRCh38.p7	11:118504756	GTAGACTAGCTGTTA[A/C/T]CTCAGACTCAGGGGA	4297
rs782271033	snp	C/G	1.67424e-05	0.00289326	missense	KMT2A	GRCh38.p7	11:118506592	ATTTGCGGACCAGTT[C/G]TTCTGAAGCACACAT	4297
rs782271167	snp	C/T	1.66471e-05	0.00288501	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473205	ATTGTTTTCGCCACT[C/T]CATTCTGGAACAAGG	4297
rs782271387	snp	A/T			missense	KMT2A	GRCh38.p7	11:118474194	GCTCCATGTTGGCTC[A/T]GGCAGACAAGCTTCC	4297
rs782271461	snp	A/T	1.65581e-05	0.00287728	missense, intron-variant	KMT2A	GRCh38.p7	11:118471801	GATCAAGAAGAAAGA[A/T]TCTAAAAGTATAGAA	4297
rs782271829	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118445136	TACATACACCTATTT[C/G]AGTGCTATAATCTTA	4297
rs782272214	snp	A/G	3.29533e-05	0.00405901	missense	KMT2A	GRCh38.p7	11:118502592	TCAGTCTCCACCACC[A/G]GGACCGCTACTGATC	4297
rs782272243	snp	C/T	3.29516e-05	0.00405891	synonymous-codon	KMT2A	GRCh38.p7	11:118505147	ACTCATAGTTGTTAA[C/T]CAGAACATGCAGCCA	4297
rs782272480	snp	C/T	1.64787e-05	0.00287038	synonymous-codon	KMT2A	GRCh38.p7	11:118484221	GCAGGAGAATGCAGG[C/T]ACTTTGAACATCCTC	4297
rs782272564	in-del	-/T	0.00414077	0.0453127	intron-variant	KMT2A	GRCh38.p7	11:118438988	TGCTGTAGATTATTA[-/T]TTTTTTTTTGAAAGG	4297
rs782272657	snp	G/T			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522830	CCCAGGAGCCTTATC[G/T]CAGCCAATTACCTTT	4297
rs782273023	snp	A/C	1.64833e-05	0.00287078	missense	KMT2A	GRCh38.p7	11:118502491	CCAGGCGTCACAGTA[A/C]CTCTTCCTTATCACC	4297
rs782273725	snp	A/G	1.67044e-05	0.00288997	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522190	CTGCTCTTCTCCCCC[A/G]GTGTTGGAGTGCAAG	4297
rs782275407	snp	A/C/G	0.000149384	0.00864116	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520777	TCCTGAAAAAAATTC[A/C/G]TTAATAGTATGTCTT	4297
rs782277230	snp	C/T	1.64806e-05	0.00287054	synonymous-codon	KMT2A	GRCh38.p7	11:118503015	TTCCCACACCTCCAT[C/T]TGAGAGGGCAAAGGA	4297
rs782278331	snp	C/T	0.000113714	0.0075395	utr-variant-5-prime	KMT2A	GRCh38.p7	11:118436508	CTTCACTTCACGGGG[C/T]GAACATGGCGCACAG	4297
rs782278463	in-del	-/AT			intron-variant	KMT2A	GRCh38.p7	11:118502305	CAGTTACCTATAAAT[-/AT]ATATATATATATAGT	4297
rs782279032	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118470283	ATGTATTTCCGGGCA[G/T]GAGTTGTTTTGTTTG	4297
rs782279632	snp	A/G	1.64863e-05	0.00287104	missense	KMT2A	GRCh38.p7	11:118468821	AAGAAGTCAGAGTGC[A/G]AAGTCCCACAAGGTC	4297
rs782280560	snp	A/G	1.66735e-05	0.00288729	synonymous-codon	KMT2A	GRCh38.p7	11:118481737	AAAGAAAGAGAAAAA[A/G]TCTAAGACCAGTGAA	4297
rs782281385	snp	A/G			missense	KMT2A	GRCh38.p7	11:118491277	GTGGAAAGTGTGATC[A/G]CTGGGTCCATTCCAA	4297
rs782281934	snp	C/T	1.66147e-05	0.0028822	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521890	CTCCCTTCTTCTGCA[C/T]GTGCAGGGCATTGGT	4297
rs782282462	snp	C/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118514694	GCTGGAGTGCAATGG[C/G]GCAATCTCGGTTCAC	4297
rs782283493	snp	C/T	1.64863e-05	0.00287104	missense, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520824	ACTAGCATGGATCTG[C/T]CAATGCCCATGCGCT	4297
rs782283835	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118457570	GCCACCATGCCTGAC[C/T]GCCTTTTTTTCCCTT	4297
rs782284425	snp	A/G	1.66991e-05	0.00288951	missense, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520027	GAATACAACCCCAAT[A/G]ATGAAGAAGAGGAGG	4297
rs782284952	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118467452	TTTTCTTAAATAGTC[C/G]AATACTTTAATCTTA	4297
rs782285342	snp	C/T	3.33578e-05	0.00408384	intron-variant	KMT2A	GRCh38.p7	11:118484352	AAGTATATTGAGTGT[C/T]AAAGACTTTAAATAA	4297
rs782286910	snp	A/G	1.69714e-05	0.00291298	intron-variant	KMT2A	GRCh38.p7	11:118489755	TTGGGTGAAGGTAAT[A/G]TGATGCTTATCTTTT	4297
rs782286998	snp	A/G	1.65091e-05	0.00287303	intron-variant, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512063	CACTCCTGTCTCAGA[A/G]TATTATGGTAAATTG	4297
rs782287256	snp	G/T	1.67835e-05	0.0028968	intron-variant	KMT2A	GRCh38.p7	11:118491366	CTAGGTACTACTACA[G/T]TTATTAGCCTCTAGA	4297
rs782287416	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118481592	TCTTTGATATACTGA[A/T]TTCCTTTATTTTGGT	4297
rs782289098	snp	A/C	1.64871e-05	0.00287111	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118472815	AACTCTACAAAGTGC[A/C]CCCCAGCAGCAGACC	4297
rs782290138	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118451385	CCTACTAATTTTTAA[G/T]TTTCTTTTCTGTTCT	4297
rs782290578	snp	G/T	1.65479e-05	0.0028764	missense, intron-variant	KMT2A	GRCh38.p7	11:118473156	TTGGCTTTGCATCTG[G/T]TTTTTCTGCATCTGG	4297
rs782291827	snp	C/T	1.64735e-05	0.00286993	missense, nc-transcript-variant, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519672	CAGTTGTGTTCCTCA[C/T]TGAGCAGCTGTCTGG	4297
rs782292919	snp	C/T	1.66974e-05	0.00288936	missense	KMT2A	GRCh38.p7	11:118495872	CCAACTCCTCTGCAT[C/T]CTCCTACACCACCAA	4297
rs782293850	snp	A/G	0.00039553	0.0140573	missense	KMT2A	GRCh38.p7	11:118506549	CTGCCTCTAGACAAA[A/G]GGAATGGCAAGAAGC	4297
rs782294071	snp	A/G	1.78096e-05	0.00298404	intron-variant	KMT2A	GRCh38.p7	11:118506653	AGGCACAGGGTGAGA[A/G]ATCCAAATACTAGCT	4297
rs782295106	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118459658	TGCTCTGACTATGGT[A/T]TATTGAAAATAATTT	4297
rs782295708	snp	A/G	1.64789e-05	0.0028704	missense, intron-variant	KMT2A	GRCh38.p7	11:118474082	GAAAAAACCAACTTG[A/G]ACCTCGGCCCAACTG	4297
rs782295732	snp	C/G	1.90729e-05	0.00308805	intron-variant	KMT2A	GRCh38.p7	11:118490100	TAAAAACAAGAAATT[C/G]CTATTGAATTTCTTT	4297
rs782296239	snp	C/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118516437	ATAGCCACGGCACCA[C/G]CTGAGCAACACAGTG	4297
rs782296522	snp	C/T	1.67312e-05	0.00289229	intron-variant	KMT2A	GRCh38.p7	11:118493024	CCTTGGTTTTAGTGT[C/T]AGATAAAAGCAACAT	4297
rs782296695	snp	A/G	1.64789e-05	0.0028704	missense	KMT2A	GRCh38.p7	11:118506199	TGCTCCCCTCCACTC[A/G]GACTACGGGCATAAC	4297
rs782296960	snp	C/T	1.64735e-05	0.00286993	synonymous-codon	KMT2A	GRCh38.p7	11:118496298	CAGTCCAGAGCTGAA[C/T]CCACCCCCAGGCATA	4297
rs782297546	in-del	-/C	0.00054482	0.0164958	frameshift-variant, intron-variant	KMT2A	GRCh38.p7	11:118473470	AGCTCTCACCTCTCA[-/C]CCCCCCCGTCTTCTG	4297
rs782297577	snp	A/G	1.70136e-05	0.00291659	intron-variant	KMT2A	GRCh38.p7	11:118498327	TAAACGTCTTAAAAC[A/G]TATGAAAGTCTGAAT	4297
rs782298490	snp	C/T	3.48341e-05	0.00417323	intron-variant	KMT2A	GRCh38.p7	11:118509936	AACCACTATCTATTT[C/T]CTCCCTATTAGAACC	4297
rs782298665	in-del	-/GCAC	1.65701e-05	0.00287833	intron-variant	KMT2A	GRCh38.p7	11:118491165	GGTATGTGAGCCAAA[-/GCAC]GCACTGCTGTAAACT	4297
rs782298668	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118445470	CTCTGAGGCTCTTCA[A/G]GGTTCTTGGGCTCCA	4297
rs782298932	snp	C/T	1.64741e-05	0.00286998	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473910	CAAAGAGAAGGTTGT[C/T]GGTGAAGATGTTGCC	4297
rs782299975	snp	C/G	3.83811e-05	0.00438053	synonymous-codon	KMT2A	GRCh38.p7	11:118436905	GCGCCGGTTCCGGGC[C/G]GTGTTTGGGGAGAGC	4297
rs782301365	snp	G/T	1.64923e-05	0.00287156	missense, intron-variant	KMT2A	GRCh38.p7	11:118473444	CAAGAAGTGGAAGGC[G/T]TAGTAGTTCTGAGCT	4297
rs782301554	snp	C/T	1.6517e-05	0.00287372	missense	KMT2A	GRCh38.p7	11:118501060	AAGATAGTGGAGTGC[C/T]GTCCTCCAGTCGTAG	4297
rs782301558	snp	C/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521691	TCTCTCCTGCAGAGA[C/T]ATTAGAAACCTCTAG	4297
rs782301834	snp	C/T			synonymous-codon	KMT2A	GRCh38.p7	11:118504709	GTCTGTCTTGACCAC[C/T]CGGAGTCCCACTGTC	4297
rs782302108	snp	A/G	1.65318e-05	0.002875	intron-variant	KMT2A	GRCh38.p7	11:118499281	GACAGCCTATTAACA[A/G]CTACCATGGGTTTTA	4297
rs782302349	snp	A/C	3.38364e-05	0.00411303	missense, intron-variant	KMT2A	GRCh38.p7	11:118472009	TCTCCTCTCAAGTCT[A/C]AGTTTAAGACAGGGA	4297
rs782302481	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118469815	AGAGTCATCATATAT[C/T]ATCATCTAATTCAAA	4297
rs782302671	in-del	-/T			intron-variant	KMT2A	GRCh38.p7	11:118494108	CCTGGCATCTCTTAA[-/T]TGCCACAGGTTAATC	4297
rs782302713	in-del	-/GGA	0.000238635	0.0109206	cds-indel	KMT2A	GRCh38.p7	11:118436563	CCCGGGACCACCGGG[-/GGA]GGCGGCGGCGGCGGG	4297
rs782302975	snp	A/G	6.28792e-05	0.00560675	intron-variant	KMT2A	GRCh38.p7	11:118488476	CTTTTTTACATAGTC[A/G]TTGCTTAATGAATAT	4297
rs782305107	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118464033	TAAAGTTTATGGGGA[A/C]AATGCCCCAAATAAA	4297
rs782306227	in-del	-/GAA			intron-variant	KMT2A	GRCh38.p7	11:118464309	AGAGGCCAAGGTGGG[-/GAA]TGGATCACCTGAGGT	4297
rs782306856	snp	A/G	1.65004e-05	0.00287227	missense	KMT2A	GRCh38.p7	11:118509997	CAGCTCCCCACTGAT[A/G]CTTTGGCTTCAGCAA	4297
rs782307765	snp	C/T	1.89468e-05	0.00307783	intron-variant	KMT2A	GRCh38.p7	11:118490101	AAAAACAAGAAATTC[C/T]TATTGAATTTCTTTT	4297
rs782308631	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118484540	AACATTCCTATCCAT[A/C]CTGAGCAGTATCAGA	4297
rs782309219	snp	A/G	6.69478e-05	0.00578528	intron-variant	KMT2A	GRCh38.p7	11:118468704	TTTGTGTCTCCTCTG[A/G]GCATTTCTTTGGGAT	4297
rs782309429	snp	C/T	1.65586e-05	0.00287733	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118472335	TGAAAAAGAAGCAGC[C/T]CAGCTGCAGGGAAGA	4297
rs782309790	snp	C/T	1.64852e-05	0.00287094	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118472830	CCCCCAGCAGCAGAC[C/T]TCCTCGTCTCCACCT	4297
rs782309823	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118508368	GCCAATTCTATTGTG[A/T]GGATCTACAATATTT	4297
rs782309932	snp	A/G	1.64991e-05	0.00287215	missense	KMT2A	GRCh38.p7	11:118491872	ATTTCTCTGAAGCAA[A/G]TTCTGACAGCTTTGT	4297
rs782310121	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520723	AAGAGTGTACTAATT[A/G]TCTCTAGGAACCTTC	4297
rs782310765	snp	A/G	1.64806e-05	0.00287054	synonymous-codon	KMT2A	GRCh38.p7	11:118503896	AGCTGAAGGACAGGT[A/G]GATGGGGCCGATGAC	4297
rs782311152	snp	C/G	1.70301e-05	0.00291801	synonymous-codon	KMT2A	GRCh38.p7	11:118482061	CACTCCTAGTGAGCC[C/G]AAGAAAAAGCAGCCT	4297
rs782311184	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118515019	TGATCTGCCCACCTC[A/G]GCCTCCCAAAGTGCT	4297
rs782311824	snp	A/C/T	6.59983e-05	0.00574416	missense	KMT2A	GRCh38.p7	11:118506102	CCTGTGGCTTTACCG[A/C/T]CAAGTTCAGGAATGT	4297
rs782312028	snp	A/G	3.33322e-05	0.00408228	synonymous-codon	KMT2A	GRCh38.p7	11:118509154	AGTCGCTGTTCTTCC[A/G]GAAGTTCAGGTGACC	4297
rs782312317	snp	C/T	1.64781e-05	0.00287033	missense, intron-variant	KMT2A	GRCh38.p7	11:118474085	AAAACCAACTTGGAC[C/T]TCGGCCCAACTGCCC	4297
rs782313440	snp	A/G	9.96463e-05	0.00705785	missense	KMT2A	GRCh38.p7	11:118436919	CCGTGTTTGGGGAGA[A/G]CGGCGGGGGAGGCGG	4297
rs782313557	snp	C/G	1.66996e-05	0.00288956	missense	KMT2A	GRCh38.p7	11:118495873	CAACTCCTCTGCATC[C/G]TCCTACACCACCAAT	4297
rs782313679	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118467251	GCATGGTGACAAGGG[C/T]CTCTAGTCTTAGCTA	4297
rs782313746	snp	A/G	3.30814e-05	0.00406689	missense, intron-variant	KMT2A	GRCh38.p7	11:118472667	TACTTCCTGAGGAGC[A/G]GAGCGATACCCCTGA	4297
rs782315435	snp	A/C	1.64768e-05	0.00287021	missense	KMT2A	GRCh38.p7	11:118503568	AGTCAACATCTCCCA[A/C]AGAACCAATTTCAGC	4297
rs782315965	snp	C/G	0.000148577	0.00861781	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118434893	ATCCCATCGTCCGCT[C/G]TGCACAAATGTTTCG	4297
rs782317770	snp	A/G	1.64732e-05	0.0028699	missense	KMT2A	GRCh38.p7	11:118496309	TGAACCCACCCCCAG[A/G]CATAGAAGACAATAG	4297
rs782318292	in-del	-/G	6.20752e-05	0.00557079	intron-variant	KMT2A	GRCh38.p7	11:118439166	CAGCAGCAAAAAAAA[-/G]AAAAAAAGAAAAAAA	4297
rs782319915	snp	A/T	1.64735e-05	0.00286993	synonymous-codon	KMT2A	GRCh38.p7	11:118498028	TGAAGATGATGACGG[A/T]TCACTAAAGAATGTG	4297
rs782320025	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118454646	GTCATAAGTCAAAGA[C/T]ACGTTTAATACACTT	4297
rs782320114	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118467376	GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	4297
rs782320299	snp	C/T	6.59065e-05	0.00574012	synonymous-codon	KMT2A	GRCh38.p7	11:118505984	GTCAGTTCCAGGACA[C/T]GTCACCTTAACCAAC	4297
rs782320376	snp	C/T	1.82101e-05	0.0030174	missense	KMT2A	GRCh38.p7	11:118494388	GCATGGTCAAGTCCT[C/T]CTTCATTCGGGTGAA	4297
rs782320999	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118452966	AAGGCCAACCTCTCC[A/G]TTTGAGCTCTGGATC	4297
rs782321171	snp	A/G	1.64814e-05	0.00287061	missense	KMT2A	GRCh38.p7	11:118501712	CACAGCTGAAATTAT[A/G]AGTCCTCCATCACCA	4297
rs782321599	snp	A/G	0.000161616	0.00898788	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118434965	ACCTTCTCTGGAGGC[A/G]TGAAGTGCACCCTCC	4297
rs782321970	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118492201	CACTTCACCCAAGAC[A/G]GTAACCTGATCAGAG	4297
rs782322487	snp	C/T	1.64738e-05	0.00286995	missense	KMT2A	GRCh38.p7	11:118506460	CTCCATCCTCTCCAT[C/T]TTCTGGACAGCGGTC	4297
rs782323062	snp	C/T	4.94189e-05	0.00497062	synonymous-codon	KMT2A	GRCh38.p7	11:118506305	TGGGATTCATTCTTC[C/T]CAGCGTGATCTTGAT	4297
rs782323193	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118459426	AAGATATAGCTGCTA[A/C]AGGGCATGTTTGAGA	4297
rs782323499	snp	C/G	4.95626e-05	0.00497784	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473817	AAAGGAGAATAAGCG[C/G]GAGTCAAGGAAAGAG	4297
rs782323910	snp	C/G	1.65132e-05	0.00287339	missense	KMT2A	GRCh38.p7	11:118478177	CCAAGTTTGGTGGTC[C/G]CAATATAAAGAAGCA	4297
rs782324036	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118506654	GGCACAGGGTGAGAG[A/T]TCCAAATACTAGCTA	4297
rs782324246	snp	C/T	3.39974e-05	0.00412281	intron-variant	KMT2A	GRCh38.p7	11:118501879	GACTTTATTGACCTA[C/T]TTGACCTAAGAAGAT	4297
rs782326801	snp	C/T	1.65002e-05	0.00287225	synonymous-codon	KMT2A	GRCh38.p7	11:118505339	TTCTCAATCTTTGTT[C/T]CCTTCTGCTAGCAAA	4297
rs782326991	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118497322	GCTTTTAAATACCAT[C/T]TGAGAGAACTGGCTT	4297
rs782327685	snp	A/G	1.65433e-05	0.002876	missense	KMT2A	GRCh38.p7	11:118502770	CTTCAGAAATGAAGC[A/G]GTCCAGTGCTTCAGA	4297
rs782327950	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118445392	GGGGTTGCTACCTGT[C/T]GTCTCTATAACTAGT	4297
rs782329775	snp	C/G	1.64887e-05	0.00287125	intron-variant	KMT2A	GRCh38.p7	11:118480258	TGTTGTTAAAAAGGT[C/G]TTCCCCCAAATGCTC	4297
rs782329968	snp	C/T	1.65364e-05	0.0028754	missense, intron-variant	KMT2A	GRCh38.p7	11:118473627	AGCAGACTAGTGCTC[C/T]GGCAGAGCCATTTTC	4297
rs782330796	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118499508	ATGACCCTCAGCCAG[C/G]TGTGGTGTCTCACGC	4297
rs782334356	snp	A/G	1.65146e-05	0.0028735	missense	KMT2A	GRCh38.p7	11:118481774	GACAGCAAAGAGAGC[A/G]GTGTTGTGAAGAACG	4297
rs782334550	snp	A/G			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118523065	CAGGAGCCATTGGTC[A/G]TAACCAGACAGAATT	4297
rs782334675	snp	A/G	1.64746e-05	0.00287002	synonymous-codon	KMT2A	GRCh38.p7	11:118502930	AACATCTAGAGAACT[A/G]AATGTTAGTAAAATC	4297
rs782335158	snp	A/C	1.65732e-05	0.00287859	missense	KMT2A	GRCh38.p7	11:118474277	TGCAAGATTGAGAAG[A/C]GTAAGAGTCTTAAAC	4297
rs782335392	snp	A/T	2.34717e-05	0.00342568	missense	KMT2A	GRCh38.p7	11:118436771	TCAGCAGCCTCCTCG[A/T]CGTCCGCCTCGTCTT	4297
rs782335823	snp	A/G	1.64893e-05	0.0028713	missense, intron-variant	KMT2A	GRCh38.p7	11:118473051	GGTCAGAGCCACAAT[A/G]CTTTTCCTCAGCAAA	4297
rs782337410	snp	G/T	1.67186e-05	0.0028912	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118472233	AAGGATTAAGCCAGT[G/T]AGGATTATTCCTTCT	4297
rs782337956	snp	C/T	1.64868e-05	0.00287109	synonymous-codon	KMT2A	GRCh38.p7	11:118504433	TGACTGTGGGAATAT[C/T]CTGCCTTCAGACATT	4297
rs782339231	snp	C/G			intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118519001	GAGAATGGCGTGAAC[C/G]CGGGAGGTGGAGCTT	4297
rs782339326	snp	A/G	1.64762e-05	0.00287016	missense, intron-variant	KMT2A	GRCh38.p7	11:118472997	GAAAATCTATTTTGC[A/G]AGAACCGACATTTAG	4297
rs782339955	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118480149	AAATTTAATTTGTTT[C/T]ATGGTTTATTCGTTG	4297
rs782340087	snp	A/G	1.79958e-05	0.0029996	intron-variant	KMT2A	GRCh38.p7	11:118490283	TTTGCCAGCTTTCGG[A/G]GGTTGTACTTGGTGT	4297
rs782343209	snp	C/T	5.02694e-05	0.0050132	intron-variant	KMT2A	GRCh38.p7	11:118491704	TTCCTCTCTCTCATT[C/T]TTCAGAGGACCTCAT	4297
rs782343352	snp	A/G	1.79832e-05	0.00299854	intron-variant	KMT2A	GRCh38.p7	11:118485019	GGAAGTACATAAATT[A/G]TTTTTCTGTGGATGA	4297
rs782343724	snp	C/G	1.64762e-05	0.00287016	missense	KMT2A	GRCh38.p7	11:118503597	GCCTCTGAAAATCCA[C/G]GAGATGGTCCAGTGG	4297
rs782345096	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118465631	GAGACCCTAAACCAA[C/T]CCTTCTCTCCCCACA	4297
rs782345273	snp	C/T	1.64917e-05	0.00287151	synonymous-codon	KMT2A	GRCh38.p7	11:118504223	GAGTTCTGTTGGCCA[C/T]AAAAATGAGCCAAAG	4297
rs782345465	snp	A/G	1.64746e-05	0.00287002	missense	KMT2A	GRCh38.p7	11:118505614	AACTTGCTCCCTCTA[A/G]TACCCCTTCAAACAT	4297
rs782345531	snp	C/T	4.31909e-05	0.00464689	intron-variant	KMT2A	GRCh38.p7	11:118494253	TTCAGAGCACACTGT[C/T]TTAAGAATAATTAAC	4297
rs782345654	snp	A/G	9.18021e-05	0.00677441	synonymous-codon	KMT2A	GRCh38.p7	11:118436581	CGGCGGCGGCGGGGG[A/G]CGCCGGGGCCTAGGG	4297
rs782346116	snp	C/T	7.01533e-05	0.00592214	intron-variant	KMT2A	GRCh38.p7	11:118495686	TAAATGCTTGTTGAA[C/T]CAATTATTTTCAGCA	4297
rs782347860	snp	C/G	3.29511e-05	0.00405887	missense	KMT2A	GRCh38.p7	11:118504938	CCTTGTGGTTCAGTA[C/G]AGCAAGGTCATGGCA	4297
rs782348341	snp	C/G	3.53682e-05	0.0042051	intron-variant	KMT2A	GRCh38.p7	11:118490112	ATTCCTATTGAATTT[C/G]TTTTCTTCTTTTCTA	4297
rs782348394	snp	C/T	3.39225e-05	0.00411826	missense, intron-variant	KMT2A	GRCh38.p7	11:118472055	GGAAGGGGGTACAAA[C/T]TGTACGACGGAGAGG	4297
rs782348668	snp	C/T	1.65362e-05	0.00287538	synonymous-codon, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520880	GGAGGCAGTTGGTGT[C/T]TACAGGTATGACTAA	4297
rs782349572	snp	C/T	3.38244e-05	0.0041123	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522210	TGGAGTGCAAGGAGG[C/T]GGGGCCATCCAAAGC	4297
rs782349849	snp	C/T			upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118525527	TTGCCGGGACCCAGC[C/T]CGCCACCCTGCTCGC	4297
rs782350135	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118497652	ATCCTACCACTTCAG[C/T]CTCCAAAAGTGCTGG	4297
rs782350466	snp	C/G	0.000132192	0.00812887	intron-variant	KMT2A	GRCh38.p7	11:118499938	ACTATAAAGAGAAGA[C/G]AGCAGCCCCACAACC	4297
rs782350622	snp	A/C	0.000702318	0.0187261	missense	KMT2A	GRCh38.p7	11:118504092	AGTGATACTAGTGTC[A/C]CAGCCACAACAAGGA	4297
rs782352824	in-del	-/CCGCTTA	1.64806e-05	0.00287054	frameshift-variant, intron-variant	KMT2A	GRCh38.p7	11:118474007	TTACTTCTGTGACTC[-/CCGCTTA]TTGGGGATACAACAG	4297
rs782352996	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118453343	ATAGATAATTCTCAG[C/T]TCTCATCTTGTTAAA	4297
rs782353352	snp	A/G	1.68564e-05	0.00290309	intron-variant	KMT2A	GRCh38.p7	11:118476767	TTATAATTTCAACAT[A/G]TATGGTTGTTATTGT	4297
rs782355924	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118463652	CAGCCAGTTTAGACA[C/T]TTAGGTTCTTTGTAG	4297
rs782355983	snp	C/T	1.6566e-05	0.00287797	synonymous-codon	KMT2A	GRCh38.p7	11:118509982	AGAGGAAAGTAATTT[C/T]AGCTCCCCACTGATG	4297
rs782357160	snp	C/T	1.64751e-05	0.00287007	synonymous-codon, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521971	TGGAAATGCTGCACG[C/T]TTCATCAATCACTCG	4297
rs782357341	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118514969	AGACGGGGTTTCACC[A/G]TGCTGGTCAGGCTAC	4297
rs782357560	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118457976	AGCCTAGGAATGGCC[A/G]ATATATATTTTAATG	4297
rs782359380	snp	C/G	1.8582e-05	0.00304806	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520078	CGGTAAGTCTTGAGT[C/G]GGGAGCAGTCATTAG	4297
rs782359683	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118471522	AAAAGAAACTAAGCA[C/T]AATTAAGATGTTTGA	4297
rs782359762	snp	A/G	8.24205e-05	0.00641899	missense	KMT2A	GRCh38.p7	11:118505406	TCCTTCCCTGCAGCT[A/G]CTCAAAGTAGTTTCC	4297
rs782360640	snp	A/C	1.65608e-05	0.00287752	missense	KMT2A	GRCh38.p7	11:118501094	CGGATATCAACAGCA[A/C]TGTTGAACATGATGA	4297
rs782362678	snp	C/T	3.367e-05	0.00410291	intron-variant	KMT2A	GRCh38.p7	11:118498357	TAGGACTCTGTTCTT[C/T]TTGGATTTTTAGAGA	4297
rs782363038	snp	C/G	3.29571e-05	0.00405924	missense	KMT2A	GRCh38.p7	11:118506208	CCACTCAGACTACGG[C/G]CATAACAGCCGCTTC	4297
rs782363211	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118443828	GCATCGGTCCAGTAG[C/G]ATTTATTTCAGGAGC	4297
rs782363512	snp	C/T	1.65356e-05	0.00287533	missense, intron-variant	KMT2A	GRCh38.p7	11:118472520	GTAGATTCAGTGCCC[C/T]GTCCTGTGGATCTTC	4297
rs782364358	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118451924	TAATGTTAACAGAAT[A/T]GTCCTTGGGAGCAAT	4297
rs782364761	snp	C/G	1.64762e-05	0.00287016	synonymous-codon	KMT2A	GRCh38.p7	11:118505705	TAATCATCCAAGTCT[C/G]TTAGATTTGGGGTCA	4297
rs782364997	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118500192	TCTTAAGATTCCTCC[-/A]AATTCCATTCATCTC	4297
rs782365456	snp	A/G	1.65839e-05	0.00287953	missense, intron-variant	KMT2A	GRCh38.p7	11:118473176	TCTGCATCTGGTACC[A/G]CTGCTTCAGCCCGAT	4297
rs782366377	snp	C/T	1.6473e-05	0.00286988	missense, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519716	CGAAATTACAAATTC[C/T]GTTTCCACAAGCCAG	4297
rs782366796	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118469682	ATTCTGACTTCATAT[A/C]TGGTTTTCTTTGATT	4297
rs782368382	snp	G/T	4.96151e-05	0.00498047	synonymous-codon	KMT2A	GRCh38.p7	11:118506572	CAAGAAGCACAAAGT[G/T]TCCCATTTGCGGACC	4297
rs782369249	snp	G/T	3.29462e-05	0.00405857	synonymous-codon	KMT2A	GRCh38.p7	11:118506293	TGCCAGCAAAACTGG[G/T]ATTCATTCTTCCCAG	4297
rs782369726	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118494068	TCATGATACAGCCAA[A/T]TTGTTTGCATTCTTA	4297
rs782370583	snp	G/T	1.65018e-05	0.00287239	synonymous-codon	KMT2A	GRCh38.p7	11:118506092	TCAGGACCAGCCTGT[G/T]GCTTTACCGCCAAGT	4297
rs782371090	snp	C/T	1.66247e-05	0.00288307	intron-variant	KMT2A	GRCh38.p7	11:118484344	TGATCATAAAGTATA[C/T]TGAGTGTCAAAGACT	4297
rs782371816	snp	A/G	3.29473e-05	0.00405864	synonymous-codon	KMT2A	GRCh38.p7	11:118505033	TCCCATCCAGAACCA[A/G]AAGTATGTGCCCAAT	4297
rs782371906	snp	G/T	3.2505e-05	0.00403131	missense	KMT2A	GRCh38.p7	11:118436864	GACGCGGCGCTGCAG[G/T]TCTCGGCCGCCATCG	4297
rs782372027	snp	G/T	1.65255e-05	0.00287445	missense	KMT2A	GRCh38.p7	11:118481893	CGTCGAGGAAAAGAG[G/T]GAAGAAGGGAATGTC	4297
rs782372675	snp	C/G	1.64887e-05	0.00287125	missense	KMT2A	GRCh38.p7	11:118505524	AGAGGACAGACCTCA[C/G]TACCACAGTAGCCAC	4297
rs782373153	snp	A/C	1.65652e-05	0.0028779	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473664	TAGTCCTACTCCTCT[A/C]TTCCCTTGGTTTACC	4297
rs782373169	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118446894	TTCTAAATTTTGAAC[C/T]GTGTCTCCTGAATGT	4297
rs782373344	snp	A/G	1.64991e-05	0.00287215	missense	KMT2A	GRCh38.p7	11:118505301	CTCACCCTTACCACA[A/G]GACTAAATCCAAGCT	4297
rs782373770	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118485160	GAGTAGCAAAGTTAT[C/T]GAGAGTGAAAAGATC	4297
rs782373846	snp	A/T	1.64743e-05	0.00287	synonymous-codon	KMT2A	GRCh38.p7	11:118506437	CAGCCCCACCTCTCC[A/T]GGGGGTTCTCCATCC	4297
rs782373978	snp	C/G	1.64757e-05	0.00287012	missense	KMT2A	GRCh38.p7	11:118501731	CCTCCATCACCAGAC[C/G]GACCTCCTCATTCAC	4297
rs782374097	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118442261	TTTGTGACTATCACT[A/G]CTTTGGGAGGAATTT	4297
rs782374753	snp	A/G	1.64787e-05	0.00287038	missense	KMT2A	GRCh38.p7	11:118476977	TGTCTTCCATGGGGA[A/G]TGATGGTAGGTCAAG	4297
rs782375454	snp	C/T	3.36468e-05	0.0041015	intron-variant	KMT2A	GRCh38.p7	11:118478218	TAAGTGGGTGTTTCA[C/T]TCTGAGATGTTGACC	4297
rs782377744	snp	A/T	3.30743e-05	0.00406645	missense	KMT2A	GRCh38.p7	11:118504119	AGGAAAAGCAGCCAG[A/T]TTCCAAAAAGAAATG	4297
rs782378727	snp	C/T	3.29462e-05	0.00405857	missense, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522054	TTGTCATCTTTGCCA[C/T]GCGTAAGATCTACCG	4297
rs782378796	snp	A/G	1.64953e-05	0.00287182	missense	KMT2A	GRCh38.p7	11:118499840	CCTTGGTCAGGGTCT[A/G]TGACAATCGACTGCT	4297
rs782379016	in-del	-/T/TT			intron-variant	KMT2A	GRCh38.p7	11:118482322	CTAGAGTTTAAATAG[-/T/TT]TTTTTTTTTTTTTTT	4297
rs782379505	snp	A/G	1.67674e-05	0.00289541	intron-variant	KMT2A	GRCh38.p7	11:118493008	AGAATTTACATGGAC[A/G]CCTTGGTTTTAGTGT	4297
rs782379558	snp	C/T	1.64868e-05	0.00287109	missense, intron-variant	KMT2A	GRCh38.p7	11:118472798	ACGACGAAAAAATTA[C/T]CAACTCTACAAAGTG	4297
rs782379755	snp	A/C	1.65411e-05	0.00287581	synonymous-codon	KMT2A	GRCh38.p7	11:118502783	GCAGTCCAGTGCTTC[A/C]GACTTGGTGTCCAAG	4297
rs782382171	snp	C/T	1.64741e-05	0.00286998	missense, intron-variant	KMT2A	GRCh38.p7	11:118474101	TCGGCCCAACTGCCC[C/T]ATCCCTGGAGAAGGA	4297
rs782382981	snp	C/G	1.83522e-05	0.00302915	intron-variant	KMT2A	GRCh38.p7	11:118502357	TTCTACACATTTGTT[C/G]TATCTACAATAGCAT	4297
rs782383599	snp	A/G	1.64961e-05	0.00287189	intron-variant	KMT2A	GRCh38.p7	11:118480268	AAGGTCTTCCCCCAA[A/G]TGCTCCTTGCTTAAA	4297
rs782385017	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118461428	CTTAATCACTGGAAG[A/C]TAAATATGAGTTAAC	4297
rs782387384	snp	C/G	3.29549e-05	0.00405911	missense	KMT2A	GRCh38.p7	11:118503582	ACAGAACCAATTTCA[C/G]CCTCTGAAAATCCAG	4297
rs782388146	snp	C/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118513105	TATATTAGCCGGCAC[C/T]GTGGCATGCACACCT	4297
rs782388617	snp	A/G	1.6661e-05	0.00288621	missense, intron-variant	KMT2A	GRCh38.p7	11:118472258	CCTTCTTCAAAAAGG[A/G]CAGATGCAACCATTG	4297
rs782388777	snp	A/G	1.6473e-05	0.00286988	missense	KMT2A	GRCh38.p7	11:118505817	CTGTTACCACAGAGT[A/G]TGGGAGGAACTGCTG	4297
rs782389309	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118470432	TTCATGACTACCAGT[C/T]TACCTTGAATGTTGT	4297
rs782390157	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118474506	GTGGCAGGACATAAC[A/G]TTCTAAGTAGAGGGA	4297
rs782391165	snp	C/G	1.68863e-05	0.00290566	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118471993	AAGAGCAGGTAAACT[C/G]TCTCCTCTCAAGTCT	4297
rs782391557	snp	C/T	1.64822e-05	0.00287068	synonymous-codon	KMT2A	GRCh38.p7	11:118504412	TTCAGACAATAACAA[C/T]AGTGATGACTGTGGG	4297
rs782392727	snp	A/G	0.000424358	0.0145602	intron-variant	KMT2A	GRCh38.p7	11:118458183	GTATCTTCTGGACTT[A/G]AGTGATTCTCCCACC	4297
rs782393372	snp	C/T	1.66308e-05	0.00288359	missense	KMT2A	GRCh38.p7	11:118507602	AAGGAGTGTGGGCAA[C/T]CTGCAGGGTAAGCTG	4297
rs782393383	snp	C/T	1.66824e-05	0.00288806	intron-variant, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519571	AGGACCATGCTGTTT[C/T]CTGTTGACTGCGCTC	4297
rs782393695	snp	A/G	1.65037e-05	0.00287256	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473595	GGAATCTGCAGAGAA[A/G]AATCAGAGACCAAGG	4297
rs782394009	snp	C/T			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118525239	GGCATCCCAAATCCC[C/T]GAGGAGTAACAGCTG	4297
rs782394137	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118455081	CACCCAGGTTGGAGC[A/G]CAGTGGCTCAGTCAG	4297
rs782394274	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118491612	CAATATGTGTCATAT[C/G]CATGAGGACATTAAA	4297
rs782394435	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118481624	TATACCTAGCTGTGG[C/G]ATTGCTGGATCATAT	4297
rs782395397	snp	G/T	1.64741e-05	0.00286998	missense	KMT2A	GRCh38.p7	11:118488645	TCTGTTGTGAGCCCT[G/T]CCACAAGTTTTGTTT	4297
rs782395415	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118467536	GCCTAGTATGCAAAG[C/G]CTGGGCCTTAAATGT	4297
rs782395671	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118459672	TATATTGAAAATAAT[G/T]TTTTTTTTTTTGAAA	4297
rs782396775	snp	C/T	1.78293e-05	0.00298569	intron-variant	KMT2A	GRCh38.p7	11:118506655	GCACAGGGTGAGAGA[C/T]CCAAATACTAGCTAG	4297
rs782397511	snp	C/T	8.24804e-05	0.00642132	missense	KMT2A	GRCh38.p7	11:118504201	GGGAGAAAGAACATG[C/T]CACTAAGAGTTCTGT	4297
rs782397592	snp	C/G	1.67069e-05	0.00289019	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522191	TGCTCTTCTCCCCCA[C/G]TGTTGGAGTGCAAGG	4297
rs782397997	snp	A/G	0.000795355	0.019926	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118434933	GGACGTAGGTTTTCA[A/G]CACCAGGAGGCTGTG	4297
rs782398305	snp	G/T	1.69189e-05	0.00290846	missense	KMT2A	GRCh38.p7	11:118494346	TTAATTCAGATGGAG[G/T]ACAGCCAGAAATTAA	4297
rs782398425	snp	A/G	1.64863e-05	0.00287104	synonymous-codon, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520826	TAGCATGGATCTGCC[A/G]ATGCCCATGCGCTTC	4297
rs782398718	snp	C/G	3.36746e-05	0.00410319	intron-variant	KMT2A	GRCh38.p7	11:118476771	AATTTCAACATGTAT[C/G]GTTGTTATTGTTTTT	4297
rs782399090	in-del	-/T	1.66128e-05	0.00288204	intron-variant	KMT2A	GRCh38.p7	11:118480146	TCTAAATTTAATTTG[-/T]TTCATGGTTTATTCG	4297
rs782399714	snp	G/T	5.4156e-05	0.00520337	intron-variant	KMT2A	GRCh38.p7	11:118490299	GGTTGTACTTGGTGT[G/T]CTGGAGGTGAACTAG	4297
rs782400603	snp	A/C	1.67413e-05	0.00289316	missense, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520032	CAACCCCAATGATGA[A/C]GAAGAGGAGGAGGTA	4297
rs782400739	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118465254	AAAAGAAAAAAAAGA[A/T]ATCTATGAAGGGCAC	4297
rs782402053	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118457746	CCCACCAGCTTTATC[A/G]TCCTTCGAAAGATTA	4297
rs782402408	snp	C/T	1.66571e-05	0.00288587	missense, intron-variant	KMT2A	GRCh38.p7	11:118473210	TTTCGCCACTCCATT[C/T]TGGAACAAGGTTTGA	4297
rs782402913	snp	A/G	9.8837e-05	0.00702914	synonymous-codon	KMT2A	GRCh38.p7	11:118505840	AACTGCTGCCACAGC[A/G]GCAGGCACATCAACA	4297
rs782403472	snp	G/T	8.30461e-05	0.0064433	intron-variant	KMT2A	GRCh38.p7	11:118491734	TCATGGTAGGTTTTT[G/T]TTTTCTTAGATGAGA	4297
rs782404733	snp	A/T	1.66021e-05	0.0028811	missense	KMT2A	GRCh38.p7	11:118482440	CAGAGCAGAGCAAAC[A/T]GAAAAAAGTGGCTCC	4297
rs782404790	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118451577	TGTTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT	4297
rs782404924	snp	A/G	1.65034e-05	0.00287253	missense	KMT2A	GRCh38.p7	11:118506562	AAGGGAATGGCAAGA[A/G]GCACAAAGTTTCCCA	4297
rs782405399	snp	A/G	1.64732e-05	0.0028699	missense	KMT2A	GRCh38.p7	11:118506312	CATTCTTCCCAGCGT[A/G]ATCTTGATTCTGCTT	4297
rs782406478	snp	A/G	1.65233e-05	0.00287426	synonymous-codon	KMT2A	GRCh38.p7	11:118474240	GGTTGCCAGCCTCCT[A/G]AAAAAGGCCAAAGCT	4297
rs782407221	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118497476	TTTTGGCTCACTGCA[A/G]TCTCGGCTTCCGGGG	4297
rs782407414	snp	A/C/T	6.59201e-05	0.00574078	synonymous-codon, missense, intron-variant	KMT2A	GRCh38.p7	11:118473956	AAAAAAGCAACAGGG[A/C/T]GGAAGAAGTCTTCAT	4297
rs782407775	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118450290	ACTATCTGAAGTAGT[A/G]CATTCATTTTGCTGT	4297
rs782408767	snp	C/T	6.62328e-05	0.00575431	intron-variant	KMT2A	GRCh38.p7	11:118499954	AGCAGCCCCACAACC[C/T]GAACACACTGAAGCC	4297
rs782409499	snp	A/G	1.64757e-05	0.00287012	missense	KMT2A	GRCh38.p7	11:118505655	GATGTGGTTTCTAAT[A/G]TGACATTGATTAACT	4297
rs782409744	snp	A/G	1.64741e-05	0.00286998	missense	KMT2A	GRCh38.p7	11:118499370	AAGGAATCAGCTTGA[A/G]AAGGAAGTTTCTCAA	4297
rs782410250	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118499611	CCAATGTGGTGAAAC[A/C]CTGTCTCTACTAAAA	4297
rs782411332	snp	A/G	1.65902e-05	0.00288008	missense	KMT2A	GRCh38.p7	11:118498403	AAGCCAGGAGCCACC[A/G]TGGGTTGCTGTCTCA	4297
rs782411723	snp	C/T	1.65869e-05	0.00287979	synonymous-codon	KMT2A	GRCh38.p7	11:118501107	CACTGTTGAACATGA[C/T]GAAAACAGGACCATT	4297
rs782411879	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118440932	CACGAAGCCTCCGAG[C/T]AGAAGTCAGTGGATG	4297
rs782412257	snp	A/C			intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118511515	AACTGTAAGGATTTT[A/C]TAGTTCTGCCTCTTA	4297
rs782412654	snp	C/T	1.6486e-05	0.00287102	synonymous-codon	KMT2A	GRCh38.p7	11:118504253	GATGGATAACTGCCA[C/T]TCTGTAAGCAGAGTT	4297
rs782413082	snp	A/G	3.29603e-05	0.00405944	missense	KMT2A	GRCh38.p7	11:118484240	TTGAACATCCTCAGC[A/G]CTCTCTCCAATGGCA	4297
rs782413640	snp	G/T	1.74802e-05	0.00295632	intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118511900	CATTGGTATTAAGAA[G/T]GGTTTACGTGCATAT	4297
rs782414041	snp	A/G			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118523007	TAGGATGTGCCTGCA[A/G]AAAGTTCCCTGAGCC	4297
rs782414402	snp	G/T	2.94816e-05	0.00383926	missense	KMT2A	GRCh38.p7	11:118436747	GTTCCAGGGGGAGCG[G/T]CCGCCGCCTCAGCAG	4297
rs782416047	snp	C/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118516793	ATATTATACCTTAAT[C/T]TGGACACCTGCACAT	4297
rs782416273	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118448851	AAGGGCAGTTTGACT[C/T]CTTAATTATAAAGTT	4297
rs782418508	snp	A/G	4.94181e-05	0.00497057	missense, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522018	ATTCTCGGGTCATCA[A/G]TATTGATGGGCAGAA	4297
rs782418763	snp	A/G			missense, intron-variant	KMT2A	GRCh38.p7	11:118472095	ATCAACAGAAAGGAT[A/G]AAGACCCCTTCGGGT	4297
rs782419238	snp	C/T	1.64757e-05	0.00287012	synonymous-codon	KMT2A	GRCh38.p7	11:118502597	CTCCACCACCGGGAC[C/T]GCTACTGATCTTGAA	4297
rs782419591	snp	A/G	1.6543e-05	0.00287597	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118472572	TCAGCACTCCTCTCA[A/G]ATGTCTTCAGACTCC	4297
rs782421006	snp	A/G	1.67273e-05	0.00289195	intron-variant	KMT2A	GRCh38.p7	11:118489772	GATGCTTATCTTTTT[A/G]CCATTATATTTTCTT	4297
rs782421888	snp	C/T	1.7364e-05	0.00294647	intron-variant	KMT2A	GRCh38.p7	11:118509939	CACTATCTATTTTCT[C/T]CCTATTAGAACCTAA	4297
rs782422569	snp	A/G	5.67972e-05	0.00532873	utr-variant-5-prime	KMT2A	GRCh38.p7	11:118436511	CACTTCACGGGGCGA[A/G]CATGGCGCACAGCTG	4297
rs782422727	snp	C/G	1.6964e-05	0.00291233	intron-variant	KMT2A	GRCh38.p7	11:118491698	CTCTTCTTCCTCTCT[C/G]TCATTCTTCAGAGGA	4297
rs782423928	snp	G/T			missense, intron-variant	KMT2A	GRCh38.p7	11:118473778	GGAGAAGGACAAGAG[G/T]AGAGAGAGAGACCGG	4297
rs782424015	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118445509	CCCATTAGTCTATAC[C/T]TGATGACATTTGTTC	4297
rs782424472	snp	A/G			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118523180	AATAGGATTTAAATC[A/G]TGCAACAACGAGAGT	4297
rs782424602	snp	C/T	1.65321e-05	0.00287502	synonymous-codon	KMT2A	GRCh38.p7	11:118502804	GGTGTCCAAGAGCTC[C/T]TCTTTAAAGGGAGAG	4297
rs782424796	snp	A/C	1.64928e-05	0.00287161	missense	KMT2A	GRCh38.p7	11:118501819	CCAGTTATTCTCCAA[A/C]ACAGAGATCCCCTGG	4297
rs782424852	snp	A/G	1.64741e-05	0.00286998	missense, intron-variant	KMT2A	GRCh38.p7	11:118473914	GAGAAGGTTGTTGGT[A/G]AAGATGTTGCCACTT	4297
rs782425097	snp	A/G	1.70583e-05	0.00292042	intron-variant	KMT2A	GRCh38.p7	11:118478239	GATGTTGACCTCTCA[A/G]CCATAAAGGTTGCTT	4297
rs782425157	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118466161	ACATAGTGAGACCCC[A/G]TCTCTGTAAATAATT	4297
rs782425462	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118475127	CAATAGAGTAAGTCT[C/G]TATCTCAAAATAAAT	4297
rs782425634	snp	C/T	1.64787e-05	0.00287038	missense	KMT2A	GRCh38.p7	11:118506205	CCTCCACTCAGACTA[C/T]GGGCATAACAGCCGC	4297
rs782426344	snp	A/C	1.68125e-05	0.00289931	intron-variant	KMT2A	GRCh38.p7	11:118484362	AGTGTCAAAGACTTT[A/C]AATAAAGAAAATGCT	4297
rs782426483	snp	C/G	1.9078e-05	0.00308847	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520088	TGAGTGGGGAGCAGT[C/G]ATTAGAAACTGCTTT	4297
rs782426529	snp	G/T	3.29484e-05	0.00405871	synonymous-codon	KMT2A	GRCh38.p7	11:118505489	TCCGGATCCCCAACT[G/T]TTGGTTTCAGAATCC	4297
rs782426604	snp	C/T	5.11165e-05	0.00505526	intron-variant	KMT2A	GRCh38.p7	11:118489936	ACCACCATGTGACTA[C/T]TGGACTTATGTAACT	4297
rs782427196	snp	C/T	1.64735e-05	0.00286993	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118474126	GAAGGAGAAAACCCT[C/T]TGCCTTTCCACTCCT	4297
rs782427944	snp	A/C	1.64822e-05	0.00287068	synonymous-codon	KMT2A	GRCh38.p7	11:118505234	TTCTGTTAGTTCTAC[A/C]CCCAGTGTGATGGAG	4297
rs782430019	snp	C/T	0.000182124	0.0095409	missense, intron-variant	KMT2A	GRCh38.p7	11:118471802	ATCAAGAAGAAAGAT[C/T]CTAAAAGTATAGAAA	4297
rs782430428	snp	A/C	1.64792e-05	0.00287042	missense	KMT2A	GRCh38.p7	11:118504732	CCACTGTCCCCAGCC[A/C]GAATCCCAGTAGACT	4297
rs782430517	snp	G/T	4.95831e-05	0.00497886	missense	KMT2A	GRCh38.p7	11:118481901	AAAAGAGTGAAGAAG[G/T]GAATGTCTCGGCCCC	4297
rs782432077	snp	C/T	1.64757e-05	0.00287012	missense	KMT2A	GRCh38.p7	11:118504986	AGGAACAGTAGCACC[C/T]CTGGCCTTCAGGTAC	4297
rs782432590	snp	C/G	1.64735e-05	0.00286993	synonymous-codon	KMT2A	GRCh38.p7	11:118505801	TTTTGAACCGGCACC[C/G]CTGTTACCACAGAGT	4297
rs782432998	snp	G/T	1.66821e-05	0.00288804	missense, intron-variant	KMT2A	GRCh38.p7	11:118473727	AGACAAGGCCCCCGA[G/T]GAGCTGTCCAAAGAT	4297
rs782433790	snp	C/T	1.66477e-05	0.00288506	missense	KMT2A	GRCh38.p7	11:118481739	AGAAAGAGAAAAAGT[C/T]TAAGACCAGTGAAAA	4297
rs782433864	snp	A/C	0.00354211	0.0419346	missense	KMT2A	GRCh38.p7	11:118506082	GCCTGGGGATTCAGG[A/C]CCAGCCTGTGGCTTT	4297
rs782434040	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118478463	GAAATGTTTAGTTCA[A/G]TATGCAGCCATTAGC	4297
rs782434088	snp	A/G	1.64738e-05	0.00286995	missense	KMT2A	GRCh38.p7	11:118501771	GCTCCTGTTATTATC[A/G]TGTCATCTCAAAGGT	4297
rs782434873	snp	A/G	1.64741e-05	0.00286998	missense	KMT2A	GRCh38.p7	11:118505575	AAAGACCCATATCTC[A/G]TCTACAGACCCGAAA	4297
rs782435022	snp	G/T	3.63981e-05	0.00426588	intron-variant	KMT2A	GRCh38.p7	11:118488547	AAGTATATAAGAAGG[G/T]TATGGTTGATTATGT	4297
rs782435447	snp	A/G	1.65299e-05	0.00287483	synonymous-codon	KMT2A	GRCh38.p7	11:118481947	ACAGGCCACCACTCC[A/G]GCTTCCAGGAAGTCA	4297
rs782436427	snp	A/T	1.65045e-05	0.00287263	intron-variant	KMT2A	GRCh38.p7	11:118480167	GGTTTATTCGTTGTT[A/T]TCCTAGGATGAGAAA	4297
rs782436496	snp	A/G	1.70072e-05	0.00291605	intron-variant	KMT2A	GRCh38.p7	11:118498329	AACGTCTTAAAACAT[A/G]TGAAAGTCTGAATAG	4297
rs782437043	snp	A/T	3.58494e-05	0.0042336	intron-variant	KMT2A	GRCh38.p7	11:118481695	TATAGACAGATGATG[A/T]TGTTGTGTTTTTCCC	4297
rs782437914	snp	A/G	1.64762e-05	0.00287016	missense	KMT2A	GRCh38.p7	11:118503432	GAAGGATCTGCCAAG[A/G]AATTACAGGCACCAC	4297
rs782438210	snp	C/G	3.29772e-05	0.00406048	missense	KMT2A	GRCh38.p7	11:118468830	GAGTGCGAAGTCCCA[C/G]AAGGTCTCCTTCAGG	4297
rs782439084	snp	A/G	4.94279e-05	0.00497107	missense, intron-variant	KMT2A	GRCh38.p7	11:118474088	ACCAACTTGGACCTC[A/G]GCCCAACTGCCCCAT	4297
rs782439470	snp	A/G	3.30808e-05	0.00406686	missense	KMT2A	GRCh38.p7	11:118503202	GGAAAAAATCCTGTA[A/G]AGAAACTTTCAAAGA	4297
rs782439948	snp	C/T	1.65151e-05	0.00287355	synonymous-codon	KMT2A	GRCh38.p7	11:118504175	AAAGATTGATAGACC[C/T]GAAGATGCTGGGGAG	4297
rs782440708	snp	C/G			missense	KMT2A	GRCh38.p7	11:118503730	AACCTCAGGAGGATG[C/G]CTCTTTTAAAAGGAG	4297
rs782442429	snp	A/G	1.67198e-05	0.0028913	missense, intron-variant	KMT2A	GRCh38.p7	11:118471713	GAAGTGGCTCTGACC[A/G]AAATTCAGCTATCCT	4297
rs782443306	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118438645	CTATTGTGCCCCGCA[C/T]CCCTTTAGATTTACG	4297
rs782444743	snp	C/T	0.000280059	0.0118301	missense	KMT2A	GRCh38.p7	11:118502992	TTTCTTCTAAAGAGG[C/T]CCTCTCCTTCCCACA	4297
rs782444905	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118509559	GATAGTCAGATTTTG[A/G]TTACAATACCAGATA	4297
rs782445787	snp	C/T	0.000157965	0.00888582	intron-variant	KMT2A	GRCh38.p7	11:118494804	TTTTTTTCTCCTCAT[C/T]GGCTAGAAATCTGAG	4297
rs782446211	snp	C/T	1.64977e-05	0.00287203	synonymous-codon	KMT2A	GRCh38.p7	11:118504067	GGATGGTGTTGATGA[C/T]GGGACAGAGAGTGAT	4297
rs782446565	snp	A/C	1.65985e-05	0.00288079	missense, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520013	ATCGTCAGCCTCCTG[A/C]ATACAACCCCAATGA	4297
rs782447123	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118509213	CAGGTATGTGGGTGG[A/G]TAAAAGGTTAGAATC	4297
rs782448566	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118468438	TGTTTCTGCCATTAT[A/C]CTTATTTGCTTACCT	4297
rs782449908	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118495091	GGTGCTTTGTACTGC[C/T]CTTGATTTTCCATAT	4297
rs782449930	snp	A/G	1.64947e-05	0.00287177	missense	KMT2A	GRCh38.p7	11:118502863	CAGAGGGATCTGCAC[A/G]TAATGTGGCTTACCC	4297
rs782450149	snp	C/T			upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118526710	CTACGAAAGACTGAA[C/T]GTAAAAGTAAAAAGT	4297
rs782450420	snp	C/T	0.000198311	0.00995571	missense, intron-variant	KMT2A	GRCh38.p7	11:118473120	ATAATTTCCGACCCC[C/T]TCCACTAACTCCCGA	4297
rs782450739	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118486340	AAATATTAAGAGTGT[A/G]GTTGGATTATGGGTG	4297
rs782451966	snp	A/C	3.29457e-05	0.00405854	synonymous-codon	KMT2A	GRCh38.p7	11:118476895	GCCCTTGGCCGAAAA[A/C]GAGCTGTGTTTCCTG	4297
rs782452561	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118479169	CAATCACCCTGTTGT[A/G]CTATCAAATGCTAAG	4297
rs782454349	snp	A/G	1.76263e-05	0.00296864	intron-variant	KMT2A	GRCh38.p7	11:118509922	GCATTTGTTACTGCA[A/G]CCACTATCTATTTTC	4297
rs782454484	snp	C/G	1.64754e-05	0.00287009	missense	KMT2A	GRCh38.p7	11:118504574	TCGTGAAAAAGACAT[C/G]GGTCTTTTTGAAGTA	4297
rs782454722	snp	C/T	1.64901e-05	0.00287137	intron-variant	KMT2A	GRCh38.p7	11:118468769	AATAATTTTCCTTTG[C/T]TGTAGGATGAGCAAT	4297
rs782455453	snp	A/G	1.65326e-05	0.00287507	missense	KMT2A	GRCh38.p7	11:118503156	ATCAACGAACATATG[A/G]GATCTAGTTCCAGAG	4297
rs782456089	snp	A/G/T	6.74427e-05	0.00580667	intron-variant	KMT2A	GRCh38.p7	11:118476765	AGTTATAATTTCAAC[A/G/T]TGTATGGTTGTTATT	4297
rs782456246	snp	C/G	1.64836e-05	0.0028708	missense	KMT2A	GRCh38.p7	11:118506013	ACCCAAGGTTGCTTG[C/G]TACCCCAGATATTGG	4297
rs782456481	snp	A/G	1.6904e-05	0.00290719	intron-variant	KMT2A	GRCh38.p7	11:118489929	ATAGAGAACCACCAT[A/G]TGACTATTGGACTTA	4297
rs782456666	snp	A/C	3.30349e-05	0.00406403	missense, intron-variant	KMT2A	GRCh38.p7	11:118472457	TTATAGAGGATGAGG[A/C]TTATGACCCTCCAAT	4297
rs782456937	snp	A/G	1.64798e-05	0.00287047	missense	KMT2A	GRCh38.p7	11:118476835	TCATCAGAGACCTCT[A/G]TGCGAGGACCCCGGA	4297
rs782457878	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118443190	AGGTAGATTATGCTG[A/G]GAATAGGGAGGAAAA	4297
rs782458108	snp	A/G	1.64901e-05	0.00287137	missense, intron-variant	KMT2A	GRCh38.p7	11:118491318	CTTTCAGGTACAGAA[A/G]GTTGGAGTCTTTTTA	4297
rs782458275	snp	C/T	3.29582e-05	0.00405931	synonymous-codon	KMT2A	GRCh38.p7	11:118504871	TGAAGGCCACATGAC[C/T]CCTGATCATTTTATC	4297
rs782459865	snp	A/G	7.64906e-05	0.00618381	synonymous-codon	KMT2A	GRCh38.p7	11:118436833	GCCGGCCCTGCTCCG[A/G]GTGGGCCCGGGCTTC	4297
rs782460416	snp	C/G			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522787	TTACCAAACATTGAG[C/G]CTGCAGGCTTTGAGT	4297
rs782460936	snp	A/G	4.95209e-05	0.00497574	missense	KMT2A	GRCh38.p7	11:118506073	GCCAGCAGAGCCTGG[A/G]GATTCAGGACCAGCC	4297
rs782461218	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118493651	ATTTTAAGTATGTAT[A/G]GGAAATGATTATTTA	4297
rs782462305	snp	G/T	3.29516e-05	0.00405891	synonymous-codon	KMT2A	GRCh38.p7	11:118503353	TAACAATGTTTCTTC[G/T]GATAAGATTGGTGAT	4297
rs782462364	snp	C/G	1.65529e-05	0.00287683	missense, intron-variant	KMT2A	GRCh38.p7	11:118472633	TCCACAGACTCTCAG[C/G]CTTCTGAGGAGATTC	4297
rs782463811	snp	C/G	4.68834e-05	0.00484144	missense	KMT2A	GRCh38.p7	11:118436724	CGGCGGGAAGCAGCG[C/G]GGCTGGGGTTCCAGG	4297
rs782465152	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118441954	CTATACCAATTGCCT[C/T]CCTTACCCTGTGGCT	4297
rs782465215	snp	A/C/G	6.58896e-05	0.00573943	synonymous-codon	KMT2A	GRCh38.p7	11:118478088	GAAAGGACGTCGATC[A/C/G]AGGCGGTGTGGGCAG	4297
rs782465551	snp	C/G	1.64808e-05	0.00287057	missense	KMT2A	GRCh38.p7	11:118484198	GAAAAACCACCTCCG[C/G]TCAATAAGCAGGAGA	4297
rs782467433	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118463076	AAAAATGACTCATTA[G/T]GTTGTTAATAATGAA	4297
rs782468587	snp	A/G	1.64738e-05	0.00286995	missense	KMT2A	GRCh38.p7	11:118505943	GTTGTATCCATGCAA[A/G]CTACCACAACCCCTA	4297
rs782468725	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118454039	TCTGTATTACATCCA[A/G]AATAAGCCCTAAATT	4297
rs782468942	snp	C/T	1.6501e-05	0.00287232	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473391	AGTGTTTAGTCCTAT[C/T]CGATCTGAACCAAGA	4297
rs782469162	snp	A/T	4.94205e-05	0.0049707	missense, nc-transcript-variant, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519666	ATGATGCAGTTGTGT[A/T]CCTCATTGAGCAGCT	4297
rs782469193	in-del	-/TCGTCC	1.67245e-05	0.00289171	cds-indel	KMT2A	GRCh38.p7	11:118436797	TCTTCGTCTTCGTCA[-/TCGTCC]TCGTCCTCAGCCTCT	4297
rs782469438	in-del	-/T	3.30816e-05	0.00406691	intron-variant	KMT2A	GRCh38.p7	11:118468870	TAAGTGCATGGTGCC[-/T]TTTTAAGTTTTGTTT	4297
rs782469546	snp	A/G	1.64996e-05	0.0028722	intron-variant	KMT2A	GRCh38.p7	11:118498088	GGTAAGACCTTATGG[A/G]TAAATTTTATGAAAG	4297
rs782470415	snp	C/T	1.7969e-05	0.00299736	intron-variant	KMT2A	GRCh38.p7	11:118498547	AGAGAGCTTTAGTTG[C/T]TTTAAAAAAAAAAAA	4297
rs782470917	snp	A/G	1.65963e-05	0.0028806	synonymous-codon	KMT2A	GRCh38.p7	11:118507535	GTGTTCCAGGACTCC[A/G]GGAGCAGAGGCTGAG	4297
rs782472065	snp	C/T	1.64765e-05	0.00287019	synonymous-codon	KMT2A	GRCh38.p7	11:118496268	ATTTCAAGGTACTGA[C/T]AGGAGTCGAGAAGAC	4297
rs782472770	snp	G/T	4.95511e-05	0.00497726	missense	KMT2A	GRCh38.p7	11:118503112	TCAAAACCTTGAAGC[G/T]ATCTGGAATGAGCAA	4297
rs782475453	snp	A/G			missense	KMT2A	GRCh38.p7	11:118503343	AACGACCATGTAACA[A/G]TGTTTCTTCTGATAA	4297
rs782475506	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118448131	TTTTGTAGTGGCTTT[A/T]TAGGAGAATACAAAT	4297
rs782476723	snp	A/G	1.6473e-05	0.00286988	missense	KMT2A	GRCh38.p7	11:118504711	CTGTCTTGACCACCC[A/G]GAGTCCCACTGTCCC	4297
rs782476945	snp	C/G	3.30808e-05	0.00406686	intron-variant	KMT2A	GRCh38.p7	11:118484320	GGACTTTAAGGTAAA[C/G]GTGTTCAGTGATCAT	4297
rs782477344	snp	C/T	1.65067e-05	0.00287282	missense, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118511963	CAGATGCCTGGAAGT[C/T]ATTGACAGATAAAGT	4297
rs782478537	snp	A/T	3.0519e-05	0.00390622	intron-variant, missense	KMT2A	GRCh38.p7	11:118439108	AGGTTACTTGCATGG[A/T]GTTGGTGCTTAAATG	4297
rs782479167	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118440056	ATAGCTCTGTATCAA[A/G]TCTTATCTGGATTCA	4297
rs782479337	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118460374	GCCCACTGCAACCTC[C/T]GTCCCCCAGGCTCAG	4297
rs782479498	snp	A/G	1.64808e-05	0.00287057	missense	KMT2A	GRCh38.p7	11:118506543	TTTCAGCTGCCTCTA[A/G]ACAAAGGGAATGGCA	4297
rs782481919	snp	C/G	1.64819e-05	0.00287066	missense	KMT2A	GRCh38.p7	11:118480205	AATCTACAATGGATG[C/G]CTTCCAAAGCCTACC	4297
rs782483401	snp	G/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512271	TCATCATCCCTAAAA[G/T]AAACCCCCTATTCAT	4297
rs782483583	snp	A/G	6.59033e-05	0.00573997	missense	KMT2A	GRCh38.p7	11:118502542	TAATGTCTCCAATGA[A/G]AACTGGGAATACTTA	4297
rs782483996	snp	A/G	3.29495e-05	0.00405877	missense	KMT2A	GRCh38.p7	11:118506264	TATCAGCTTCAGCAT[A/G]TGAACCAGCTCCTTG	4297
rs782485631	snp	C/G	1.64895e-05	0.00287132	missense, intron-variant	KMT2A	GRCh38.p7	11:118472762	AGGTATTCAGTGTCG[C/G]AGAGAAGTTTTGGAT	4297
rs782486737	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118490898	CAAATGTGTGAGAAA[C/G]TTCTCTCTTCCATTC	4297
rs782486872	snp	A/G	1.64849e-05	0.00287092	missense	KMT2A	GRCh38.p7	11:118484940	ATAACACCCAGGGTG[A/G]TTTGCTTTCTCTGTG	4297
rs782487109	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118488337	CATAGCTCTTTGTTT[A/T]TACCACTCTTAGGTC	4297
rs782489094	snp	C/T	1.75191e-05	0.0029596	intron-variant	KMT2A	GRCh38.p7	11:118481708	TGTTGTTGTGTTTTT[C/T]CCTCAGCTGTGAAAA	4297
rs782489222	snp	C/T	1.64882e-05	0.00287121	missense	KMT2A	GRCh38.p7	11:118502877	CATAATGTGGCTTAC[C/T]CTGGAATTCCTAAAC	4297
rs782490280	snp	A/G	1.6501e-05	0.00287232	synonymous-codon	KMT2A	GRCh38.p7	11:118474222	TCCAATGACTGACAA[A/G]AGGGTTGCCAGCCTC	4297
rs782490618	snp	A/C	1.64787e-05	0.00287038	synonymous-codon	KMT2A	GRCh38.p7	11:118503005	GGCCCTCTCCTTCCC[A/C]CACCTCCATTTGAGA	4297
rs782490706	snp	C/T	3.30513e-05	0.00406504	synonymous-codon	KMT2A	GRCh38.p7	11:118510078	TGTTTTTGAAATTTC[C/T]AGTGATGATGGCTTT	4297
rs782490771	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118509408	ATTGTGTGATCACCT[A/G]TCAGCTAAGGACTCA	4297
rs782491835	snp	C/G	8.28288e-05	0.00643487	missense	KMT2A	GRCh38.p7	11:118481987	GTCTCCCAGCCAGCA[C/G]TGGTCATCCCGCCTC	4297
rs782491860	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118496788	TTCTGTGCTTAACTG[C/T]CTACTTATTGACTTT	4297
rs782491946	snp	C/T	6.30975e-05	0.00561647	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118436480	CCTGTGTTGTCGCCT[C/T]TCCCTCTCGCTGCTT	4297
rs782494435	snp	A/G	9.88403e-05	0.00702925	missense	KMT2A	GRCh38.p7	11:118505083	CGTCTCAGATTTCCA[A/G]TGCAGCTGTCCAGAC	4297
rs782494615	snp	C/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521472	GCTGTAGAAAGGGAC[C/T]AGTATGACCCCTGGA	4297
rs782495161	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118481036	CAATGGGTAATAATC[A/G]CATCAGGGTACATGG	4297
rs782495468	snp	A/T	1.64939e-05	0.0028717	synonymous-codon	KMT2A	GRCh38.p7	11:118505279	ATTGGGACCCATGGG[A/T]GGTGGTCTCACCCTT	4297
rs782495804	snp	C/T	1.64784e-05	0.00287035	missense	KMT2A	GRCh38.p7	11:118503555	CCTTTGCAAATAGAG[C/T]CAACATCTCCCACAG	4297
rs782496408	snp	C/G	8.9815e-05	0.0067007	synonymous-codon	KMT2A	GRCh38.p7	11:118436809	GTCATCGTCCTCAGC[C/G]TCTTCAGGGCCGGCC	4297
rs782497028	snp	G/T	9.88794e-05	0.00703064	missense	KMT2A	GRCh38.p7	11:118503847	ACATTCCATTCTACA[G/T]CAGCTCAACTGGGAA	4297
rs782497639	snp	A/G			synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473829	GCGGGAGTCAAGGAA[A/G]GAGAAAAGGAAAAAG	4297
rs782497834	snp	G/T	1.65135e-05	0.00287341	intron-variant	KMT2A	GRCh38.p7	11:118493246	GTATGTTTCTACAGT[G/T]AGCCATCAGAATTTC	4297
rs782498012	snp	C/G	1.64781e-05	0.00287033	missense	KMT2A	GRCh38.p7	11:118484209	TCCGGTCAATAAGCA[C/G]GAGAATGCAGGCACT	4297
rs782499672	snp	C/T	1.64751e-05	0.00287007	missense	KMT2A	GRCh38.p7	11:118491839	GAGTGGCGACTGGCC[C/T]TTGAAAAAGAGCTGC	4297
rs782499682	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118511013	CCATGTGAGGTAATA[C/G]TGAAAGAGAAAATTG	4297
rs782499842	snp	C/T	1.65192e-05	0.00287391	missense, intron-variant	KMT2A	GRCh38.p7	11:118472468	GAGGATTATGACCCT[C/T]CAATTAAAATTGCCC	4297
rs782500523	snp	C/T	1.67837e-05	0.00289682	intron-variant	KMT2A	GRCh38.p7	11:118491364	TTCTAGGTACTACTA[C/T]ATTTATTAGCCTCTA	4297
rs782500667	in-del	-/G	3.30175e-05	0.00406296	intron-variant	KMT2A	GRCh38.p7	11:118499289	ATTAACAGCTACCAT[-/G]GGTTTTATTTAAGGT	4297
rs782500897	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118498646	GCCCCCTGCACCCAC[A/G]TATGCACAGCCTCCC	4297
rs782500964	snp	A/G	1.64732e-05	0.0028699	missense, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521337	AGAAACATTGATGCA[A/G]GTGAGATGGTGATTG	4297
rs782502223	snp	A/G	1.65337e-05	0.00287517	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473136	TCCACTAACTCCCGA[A/G]GACGTTGGCTTTGCA	4297
rs782502838	snp	C/G	1.64885e-05	0.00287123	missense	KMT2A	GRCh38.p7	11:118489859	GACCAAACTACCCCA[C/G]CAAACCCACAAAGAA	4297
rs782502879	snp	C/T	1.64874e-05	0.00287113	missense	KMT2A	GRCh38.p7	11:118502484	ATTGGCTCCAGGCGT[C/T]ACAGTACCTCTTCCT	4297
rs782503325	snp	A/G	1.64735e-05	0.00286993	missense, intron-variant	KMT2A	GRCh38.p7	11:118472927	CTTATGCCTCCAACA[A/G]TCCCCTTAGCATCAC	4297
rs782503601	snp	C/G/T	4.94607e-05	0.00497276	synonymous-codon	KMT2A	GRCh38.p7	11:118468798	ATTCTTAGGTTTTGG[C/G/T]TCAGATGAAGAAGTC	4297
rs782503918	in-del	-/TTTTG			intron-variant	KMT2A	GRCh38.p7	11:118462317	TACTTAGTTTTTTTG[-/TTTTG]TTTTGTTTTGTTTTG	4297
rs782504564	snp	A/G	1.65496e-05	0.00287655	missense, intron-variant	KMT2A	GRCh38.p7	11:118471773	ATAAATCAGAGACCA[A/G]ATCTGGAGATAAGAT	4297
rs782504650	snp	A/T	1.64863e-05	0.00287104	intron-variant	KMT2A	GRCh38.p7	11:118488577	TTTTTCTACATATTA[A/T]TTGACATACTTCTAT	4297
rs782505642	snp	A/G	0.000197778	0.00994234	synonymous-codon	KMT2A	GRCh38.p7	11:118506167	TGCTGCAATAACAGC[A/G]GCATCTAGCATCTGT	4297
rs782505711	in-del	-/A	1.76484e-05	0.0029705	intron-variant	KMT2A	GRCh38.p7	11:118490255	TTGCTAAAGGTACCC[-/A]AAAAAAGCCAGTTTT	4297
rs782505839	snp	A/C	3.29609e-05	0.00405948	missense	KMT2A	GRCh38.p7	11:118504032	GAGGAACAGTGTGAT[A/C]TTCCAAAAATCTCAC	4297
rs782506181	snp	A/G	1.77574e-05	0.00297966	intron-variant	KMT2A	GRCh38.p7	11:118509907	GTCAGTGCTCAGTGA[A/G]CATTTGTTACTGCAA	4297
rs782507041	snp	A/T	1.65296e-05	0.00287481	synonymous-codon	KMT2A	GRCh38.p7	11:118507562	TGAGCAGCAGGATAC[A/T]GCTAGCGTGGAGCAG	4297
rs782508225	snp	A/G	1.65866e-05	0.00287976	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519832	CAGTTTTGGGTCTCG[A/G]TTTTCTTATCTCATG	4297
rs782508310	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118518343	ATAAATGTTGTTTTC[A/G]TAAAATAAAAATAAA	4297
rs782508319	snp	C/T	1.93845e-05	0.00311318	intron-variant	KMT2A	GRCh38.p7	11:118488812	TGTATCAGTGGGTTC[C/T]GTATCCCTGGACTCA	4297
rs782508679	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118457423	AGGTGCCCACCACCA[C/T]GCCTGGCTAATTTTT	4297
rs782509176	snp	C/G	4.99729e-05	0.0049984	missense, intron-variant	KMT2A	GRCh38.p7	11:118473715	AGGGAGAAATAAAGA[C/G]AAGGCCCCCGAGGAG	4297
rs782509272	snp	C/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118515921	TCGAACTTCTGACCT[C/T]AGGTAATCTACCCAC	4297
rs782509432	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118445166	AGAATGTTCTTGATA[C/T]TAGTCTGAGTGTCAA	4297
rs782509729	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118479653	ATAAAGTTGCATTAA[A/C]TTTAAGAGTTAAAGT	4297
rs782510356	in-del	-/A	7.65492e-05	0.00618617	intron-variant	KMT2A	GRCh38.p7	11:118438988	TTGCTGTAGATTATT[-/A]TTTTTTTTTGAAAGG	4297
rs782510721	snp	A/G	3.30447e-05	0.00406464	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521466	TGTTTTGCTGTAGAA[A/G]GGGACCAGTATGACC	4297
rs782511279	snp	C/T	1.6483e-05	0.00287076	synonymous-codon	KMT2A	GRCh38.p7	11:118504421	TAACAACAGTGATGA[C/T]TGTGGGAATATCCTG	4297
rs782511879	snp	A/G	1.64762e-05	0.00287016	synonymous-codon	KMT2A	GRCh38.p7	11:118506515	CACTAAACCCAAACC[A/G]AAAACCAAACGGTTT	4297
rs782512444	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118497165	ATGTGCCACCATGCC[C/T]GGCTAATTTTGTATT	4297
rs782512467	snp	A/G	1.65773e-05	0.00287895	intron-variant	KMT2A	GRCh38.p7	11:118499259	TCATAAGTATAATGT[A/G]CAAAGGGACAGCCTA	4297
rs782512555	snp	A/T	1.72502e-05	0.0029368	intron-variant	KMT2A	GRCh38.p7	11:118494789	GAATTTAGCATAACT[A/T]TTTTTTCTCCTCATC	4297
rs782513413	snp	A/G	1.70232e-05	0.00291741	missense, intron-variant	KMT2A	GRCh38.p7	11:118472144	CTGGAAAAGCCCCAG[A/G]AAGTCCGGAAAGACA	4297
rs782513935	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118455784	CTCACTGCAACCTTG[A/C]CCTCCTGGGCTCTGG	4297
rs782513958	snp	A/G	1.64931e-05	0.00287163	synonymous-codon	KMT2A	GRCh38.p7	11:118499893	CGACTGTGAAGATAA[A/G]CTCTTTCCTATTGGA	4297
rs782517007	snp	C/G	1.64806e-05	0.00287054	missense, intron-variant	KMT2A	GRCh38.p7	11:118474067	GGGAGAGGAAATCTG[C/G]AAAAAACCAACTTGG	4297
rs782517476	snp	C/T	1.64988e-05	0.00287213	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473490	CCCGTCTTCTGTCTC[C/T]TCCTCGTTAAGCATT	4297
rs782517973	snp	A/T	1.65002e-05	0.00287225	synonymous-codon	KMT2A	GRCh38.p7	11:118505348	TTTGTTCCCTTCTGC[A/T]AGCAAAGGATTGCTA	4297
rs782519433	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118452779	GCTGGGATTACAGGC[A/G]CCCACCACCACGCCC	4297
rs782519862	snp	C/T	1.6477e-05	0.00287024	synonymous-codon	KMT2A	GRCh38.p7	11:118502558	AACTGGGAATACTTA[C/T]TCTAGGAATAATGTT	4297
rs782521121	snp	A/G	1.65091e-05	0.00287303	intron-variant	KMT2A	GRCh38.p7	11:118484162	GTGATTTTGTTCTAT[A/G]TTCATCTTTTGTCTC	4297
rs782521888	snp	C/T	1.65501e-05	0.00287659	missense, intron-variant	KMT2A	GRCh38.p7	11:118472616	GCCCCAGTGTTGATA[C/T]CTCCACAGACTCTCA	4297
rs782521960	snp	C/T	0.000116137	0.00761939	missense	KMT2A	GRCh38.p7	11:118482006	TCATCCCGCCTCAGC[C/T]ACCTACTACAGGACC	4297
rs782522865	snp	A/G	3.29995e-05	0.00406185	synonymous-codon	KMT2A	GRCh38.p7	11:118501041	GCGCTGTGTATATAC[A/G]TGCAAGATAGTGGAG	4297
rs782523334	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118489127	ACTTGGGAGGCTGAG[C/G]GAGGAAAATCGCTTG	4297
rs782524513	snp	C/T	3.29511e-05	0.00405887	missense	KMT2A	GRCh38.p7	11:118502974	AACCCTCTTCAGTGT[C/T]GTTTTCTTCTAAAGA	4297
rs782524769	snp	A/T	1.64743e-05	0.00287	synonymous-codon	KMT2A	GRCh38.p7	11:118505603	AAAGAATAAAAAACT[A/T]GCTCCCTCTAGTACC	4297
rs782525125	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118443419	TACCTTGTCAGGTTA[C/T]ACACCAGGGGAAGCC	4297
rs782526007	snp	C/T	1.65307e-05	0.0028749	synonymous-codon	KMT2A	GRCh38.p7	11:118502717	AAGGACAGTGGTTAC[C/T]GTAGGCAATAAAAAC	4297
rs782526178	snp	A/G	1.64914e-05	0.00287149	missense	KMT2A	GRCh38.p7	11:118505269	ATACTTCAGTATTGG[A/G]ACCCATGGGAGGTGG	4297
rs782526334	snp	A/G	1.6473e-05	0.00286988	synonymous-codon	KMT2A	GRCh38.p7	11:118476867	TAAACATGTCTGCAG[A/G]AGAGCAGCTGTTGCC	4297
rs782526423	snp	A/G	1.64741e-05	0.00286998	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473889	GTATCCTGTGGGTAG[A/G]GTTTCCAAAGAGAAG	4297
rs782526778	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118447712	TGGAAGTCAGTCCTA[C/T]GAGGAAAGGTTGAGA	4297
rs782527192	snp	A/G	1.64933e-05	0.00287165	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473427	TTCTCACTCCATGAG[A/G]ACAAGAAGTGGAAGG	4297
rs782527592	snp	C/T	4.99588e-05	0.00499769	missense	KMT2A	GRCh38.p7	11:118495863	CCAGACTCACCAACT[C/T]CTCTGCATCCTCCTA	4297
rs782528203	snp	C/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118514868	GAACTCCTGACCTCA[C/G]GTAATCTGCCCGCCT	4297
rs782529723	snp	A/G			upstream-variant-2KB, downstream-variant-500B, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118527194	ACTGAAAGCATTTCA[A/G]GGAGAAGCTGGAGAA	4297
rs782530588	snp	C/T	1.6477e-05	0.00287024	synonymous-codon	KMT2A	GRCh38.p7	11:118505450	CAATCCTCCTTCAGG[C/T]CTGCTTATTGGGGTT	4297
rs782531013	snp	C/T	0.000148245	0.00860815	synonymous-codon	KMT2A	GRCh38.p7	11:118505901	GGGTCTGTGTCTGGC[C/T]TGGCATCCAGTTCCT	4297
rs782531805	snp	A/G/T	0.000205604	0.0101374	synonymous-codon	KMT2A	GRCh38.p7	11:118436716	GGCGGCGGCGGCGGG[A/G/T]AGCAGCGGGGCTGGG	4297
rs782532585	snp	A/C	0.00016815	0.0091677	intron-variant	KMT2A	GRCh38.p7	11:118439155	TTTTAAAAGATACAG[A/C]AGCAAAAAAAAAAAA	4297
rs782532613	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118441839	ACAATAGTGATCCAT[A/C]TTCTTATTGGAAGTT	4297
rs782532794	snp	A/G	1.64741e-05	0.00286998	missense	KMT2A	GRCh38.p7	11:118504630	AACCTGTGGATAGTA[A/G]TGTCTCTTCCTCTAT	4297
rs782533062	snp	C/G	1.65143e-05	0.00287348	missense	KMT2A	GRCh38.p7	11:118504087	CAGAGAGTGATACTA[C/G]TGTCACAGCCACAAC	4297
rs782533855	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118463298	TTTATTACCTGTTGA[A/T]TACTTTACCTATTGA	4297
rs782534757	snp	A/T	0.000140538	0.00838149	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118434726	GCTGTAACAACGGAA[A/T]CTTGTTCTGTGTATT	4297
rs782534802	snp	A/G	1.65222e-05	0.00287417	synonymous-codon	KMT2A	GRCh38.p7	11:118481860	GAAAAGCAGTAGTGA[A/G]CCTCCTCCACGAAAG	4297
rs782535052	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118475560	AACCCTGTCTCTACT[A/G]AAAATCCAAAAAATT	4297
rs782535422	snp	C/T	3.34549e-05	0.00408978	missense, intron-variant	KMT2A	GRCh38.p7	11:118471947	GGACACCTTCTGCTA[C/T]GTTTCAGCAAGCCAC	4297
rs782535595	snp	G/T	3.29457e-05	0.00405854	synonymous-codon, nc-transcript-variant, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519685	CATTGAGCAGCTGTC[G/T]GGTGCCAAGCACTGT	4297
rs782536016	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118514210	TATTAGTAAATATTT[A/G]CTGACCACTTGTAAA	4297
rs782536573	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118480810	TGGGACTACAGGTGC[A/G]CACCACCACGCCCAG	4297
rs782537837	in-del	-/A	0.000181835	0.00953333	intron-variant	KMT2A	GRCh38.p7	11:118439157	TAAAAGATACAGCAG[-/A]CAAAAAAAAAAAAAA	4297
rs782538080	snp	G/T			missense	KMT2A	GRCh38.p7	11:118501779	TATTATCATGTCATC[G/T]CAAAGGTCCCCAGGA	4297
rs782538380	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520185	TTTAAAAGGACTGAA[A/G]ACCATTTGTGTTGAA	4297
rs782539046	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118456329	TCATCTCTACTAAAA[A/T]TTTAAAAAATGAACC	4297
rs782539624	snp	G/T	1.64781e-05	0.00287033	missense	KMT2A	GRCh38.p7	11:118503544	GTCCTGCTTCCCCTT[G/T]GCAAATAGAGTCAAC	4297
rs782540221	snp	A/C	1.64939e-05	0.0028717	missense	KMT2A	GRCh38.p7	11:118501698	AAAGAGAGTCAAAAC[A/C]CAGCTGAAATTATAA	4297
rs782540496	snp	A/C	3.30033e-05	0.00406209	synonymous-codon, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521920	TTGCTATATGTTCCG[A/C]ATTGATGACTCAGAG	4297
rs782541228	snp	A/G	1.64743e-05	0.00287	synonymous-codon, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521306	TCCCATCCATGGCCG[A/G]GGTCTTTTCTGTAAG	4297
rs782541447	snp	A/G	7.06972e-05	0.00594505	synonymous-codon	KMT2A	GRCh38.p7	11:118436821	AGCCTCTTCAGGGCC[A/G]GCCCTGCTCCGGGTG	4297
rs782541963	snp	C/T	1.74573e-05	0.00295438	intron-variant	KMT2A	GRCh38.p7	11:118495945	TCTAGATGCAGATGA[C/T]TGACTTCGTGAATCC	4297
rs782542236	snp	A/G	3.30518e-05	0.00406507	missense	KMT2A	GRCh38.p7	11:118503144	AGATCATCCATTATC[A/G]ACGAACATATGGGAT	4297
rs782542399	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118471300	TTGGTGGCTAGGATA[C/T]GGCGAGGAAGTTCAG	4297
rs782543327	snp	A/C/G	3.30372e-05	0.0040642	missense	KMT2A	GRCh38.p7	11:118495815	TTAATGAAGAAAATC[A/C/G]TTCCAGCTCCCAAAC	4297
rs782544004	snp	C/G	1.79432e-05	0.00299521	intron-variant	KMT2A	GRCh38.p7	11:118490275	AAGCCAGTTTTGCCA[C/G]CTTTCGGAGGTTGTA	4297
rs782546456	in-del	-/T	1.77732e-05	0.00298099	intron-variant	KMT2A	GRCh38.p7	11:118488783	ACTTGGTAATAGAAC[-/T]ACAGCTGGGCCTCTG	4297
rs782546469	snp	C/G	1.67447e-05	0.00289345	intron-variant	KMT2A	GRCh38.p7	11:118484985	GTAGAGGTAAGGCAT[C/G]CTGCTTCTTTGTACC	4297
rs782547369	snp	C/G	1.64974e-05	0.00287201	missense, intron-variant	KMT2A	GRCh38.p7	11:118473515	AGCATTTCTGTTAGT[C/G]CTCTTGCCACTAGTG	4297
rs782547460	in-del	-/AA			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118517393	GGGTGAGACTCTGTC[-/AA]TCAAAAAAAAAAAAA	4297
rs782548783	snp	A/G	1.6681e-05	0.00288794	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520767	AAACATTATTTCCTG[A/G]AAAAAATTCGTTAAT	4297
rs782548809	snp	C/T	6.58946e-05	0.0057396	missense, intron-variant	KMT2A	GRCh38.p7	11:118472966	CCTGCTTCCACTGCT[C/T]CTATGCAAGGGAAGC	4297
rs782549032	snp	A/T	1.80016e-05	0.00300008	intron-variant	KMT2A	GRCh38.p7	11:118509110	GAACTAGCTGATATT[A/T]TATCTTACATTTGGT	4297
rs782549981	snp	A/G	1.66291e-05	0.00288345	intron-variant	KMT2A	GRCh38.p7	11:118497895	AAAACCTCCTTTGGC[A/G]TTATATTCTTTAGGA	4297
rs782550041	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118464599	ATGGGTGCCAAAACC[A/G]TTGCACCCAAATCAG	4297
rs782550245	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512382	AAATGAAATCAGACA[A/G]TATGTAGCCTTTTGT	4297
rs782550908	snp	A/T	1.6492e-05	0.00287154	missense	KMT2A	GRCh38.p7	11:118506415	CTTTATCCTCAGCTG[A/T]GCAAGCCAGCCCCAC	4297
rs782551269	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118510664	TCACTCACTCAACAG[C/T]GAGCTCTCCATAAGG	4297
rs782551459	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118466838	AAAAACAACAAAAAA[A/C]CAACAAAAAAAGAAC	4297
rs782551573	snp	C/T	1.64811e-05	0.00287059	missense	KMT2A	GRCh38.p7	11:118474185	CCTCCATAGGCTCCA[C/T]GTTGGCTCAGGCAGA	4297
rs782551612	snp	C/T	3.32447e-05	0.00407691	synonymous-codon	KMT2A	GRCh38.p7	11:118498513	CCAACGACATCGGGA[C/T]TTGATCAAAGGCGAA	4297
rs782553179	snp	A/G	3.6505e-05	0.00427214	intron-variant	KMT2A	GRCh38.p7	11:118471654	CATTGTTTAATTTCT[A/G]TACACAGTTAAAACT	4297
rs782555285	in-del	-/T	1.66305e-05	0.00288357	intron-variant	KMT2A	GRCh38.p7	11:118500963	TCTCCCTTATGATGA[-/T]TTTTCCCAAATCTGT	4297
rs782555430	snp	A/G	1.65064e-05	0.00287279	missense, intron-variant	KMT2A	GRCh38.p7	11:118472733	AAAATGAGAGTAATG[A/G]TAGGAGAAGCAGAAG	4297
rs782556163	snp	A/G	0.000164745	0.00907442	missense	KMT2A	GRCh38.p7	11:118503367	CTGATAAGATTGGTG[A/G]TAAAGGCCTTTCTAT	4297
rs782556267	snp	G/T	1.64817e-05	0.00287064	intron-variant	KMT2A	GRCh38.p7	11:118488594	TGACATACTTCTATC[G/T]TCCCATGTTCTTACT	4297
rs782556543	snp	C/T	4.94197e-05	0.00497066	synonymous-codon	KMT2A	GRCh38.p7	11:118478010	TGCTGAACCTCTTGC[C/T]CCACCCATCAAACCA	4297
rs782556948	snp	C/G			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522502	TGTTGGGAGATTGGG[C/G]CTGAATTTCTCCACA	4297
rs782557235	snp	A/C/G/T	0.000393038	0.0140133	intron-variant	KMT2A	GRCh38.p7	11:118501637	GATATTTTAATTGGG[A/C/G/T]CTTTTTAGTTAAGAG	4297
rs782557321	snp	A/G	1.65304e-05	0.00287488	missense	KMT2A	GRCh38.p7	11:118507557	GAGGCTGAGCAGCAG[A/G]ATACAGCTAGCGTGG	4297
rs782558955	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118446694	ACTTTTGGATAGTTT[A/T]TTGTGGTAATCTTCT	4297
rs782558969	snp	C/G	3.29468e-05	0.00405861	synonymous-codon	KMT2A	GRCh38.p7	11:118505954	GCAAACTACCACAAC[C/G]CCTACAAGTAGTGCG	4297
rs782559329	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118458946	TACTAGAAGCCTTCA[A/G]AACAAAGTATTTCAA	4297
rs782559798	snp	C/T			upstream-variant-2KB, downstream-variant-500B, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118526880	GAGGGTGGAGAAAAG[C/T]GGGAGGGGCATGGCC	4297
rs782560620	snp	C/T	1.69275e-05	0.0029092	missense, intron-variant	KMT2A	GRCh38.p7	11:118472175	AGGAAGGAACACCTC[C/T]ACTTACAAAAGAAGA	4297
rs782561563	snp	C/T	1.64735e-05	0.00286993	synonymous-codon, nc-transcript-variant, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519670	TGCAGTTGTGTTCCT[C/T]ATTGAGCAGCTGTCT	4297
rs782561971	snp	A/G	1.6534e-05	0.00287519	intron-variant	KMT2A	GRCh38.p7	11:118493264	CCATCAGAATTTCTA[A/G]TGCCAATAAAGCTTC	4297
rs782563370	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118514586	GCTGGGACTACAGGC[A/G]CATGCTACCACACCC	4297
rs782563918	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118451296	AGCTCACTGCAGCCT[C/T]AAACTCCTGGGCTCA	4297
rs782564633	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118453039	CATCTCTCCTGCTGC[A/G]TAGGTAATTTCTCTC	4297
rs782565049	snp	A/G	1.65064e-05	0.00287279	intron-variant	KMT2A	GRCh38.p7	11:118496212	AGACATAGTATTGCC[A/G]ATTTTAACTGGATCT	4297
rs782565214	snp	C/T	1.64936e-05	0.00287168	missense	KMT2A	GRCh38.p7	11:118468838	AGTCCCACAAGGTCT[C/T]CTTCAGGTACGGCCA	4297
rs782565279	snp	A/G			synonymous-codon	KMT2A	GRCh38.p7	11:118504676	GTTTGAGTTGCCTCT[A/G]GAGCTACCATCTGAT	4297
rs782565480	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118497423	CCTTTTGAGACCAGG[C/T]CTTGCTCTGTCACCC	4297
rs782566884	snp	C/G	1.64925e-05	0.00287158	intron-variant	KMT2A	GRCh38.p7	11:118491958	ATTTTTTTCTGAGAG[C/G]TTGTTCTTAGGTAGT	4297
rs782567126	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118509562	AGTCAGATTTTGGTT[A/G]CAATACCAGATACAT	4297
rs782567500	snp	C/T	3.4534e-05	0.00415521	intron-variant	KMT2A	GRCh38.p7	11:118510156	ACCCATCAGCAGAAG[C/T]CCTGTTTCAGCTAGA	4297
rs782567752	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118477197	AGCTGTCAGACTGTG[C/T]TGCCCATCTCACCCC	4297
rs782567761	snp	C/T	3.30366e-05	0.00406413	intron-variant	KMT2A	GRCh38.p7	11:118499441	ACCTAGCCTTGGTTA[C/T]TGGGGAAGGCTGTAT	4297
rs782567920	in-del	-/T	1.80172e-05	0.00300138	intron-variant	KMT2A	GRCh38.p7	11:118502393	ACTTTTTCTCTCTTG[-/T]TTAGGAAGTCCTACC	4297
rs782568864	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118459632	GTAAAGAACTCTAGG[C/T]GGGTGATTTTTGCTC	4297
rs782569880	snp	C/G	3.30109e-05	0.00406256	intron-variant	KMT2A	GRCh38.p7	11:118499432	ATTGGTATGACCTAG[C/G]CTTGGTTATTGGGGA	4297
rs782570144	snp	C/T	8.25784e-05	0.00642514	missense	KMT2A	GRCh38.p7	11:118502680	GTTTAGGGCAAAACA[C/T]TTCCACCTCTTCAAA	4297
rs782570546	snp	A/G	3.52063e-05	0.00419546	intron-variant	KMT2A	GRCh38.p7	11:118494805	TTTTTTCTCCTCATC[A/G]GCTAGAAATCTGAGA	4297
rs782571190	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118439167	CAGCAGCAAAAAAAA[A/G]AAAAAAGAAAAAAAA	4297
rs782571627	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521641	TGAGTGGCTCCTAGT[A/G]TCAGAAGCAAATAGC	4297
rs782573096	snp	C/T	3.38198e-05	0.00411202	missense, intron-variant	KMT2A	GRCh38.p7	11:118472181	GAACACCTCCACTTA[C/T]AAAAGAAGATAAGAC	4297
rs782573731	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118442871	TAGATCTACATGTGG[C/T]ATGCTAGAGAAAATG	4297
rs782574080	snp	C/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520122	TCTCCTCCAGCTGGT[C/T]AGGGCACTACGTAGG	4297
rs782575526	snp	A/C	1.77118e-05	0.00297583	synonymous-codon	KMT2A	GRCh38.p7	11:118506644	CCTGACCTCAGGCAC[A/C]GGGTGAGAGATCCAA	4297
rs782575685	snp	A/G	3.30055e-05	0.00406222	missense, intron-variant	KMT2A	GRCh38.p7	11:118472739	AGAGTAATGATAGGA[A/G]AAGCAGAAGGTATTC	4297
rs782575816	snp	C/T	1.92944e-05	0.00310593	utr-variant-5-prime	KMT2A	GRCh38.p7	11:118436512	ACTTCACGGGGCGAA[C/T]ATGGCGCACAGCTGT	4297
rs782576050	snp	A/T	6.61113e-05	0.00574903	missense, intron-variant	KMT2A	GRCh38.p7	11:118472502	TAGAGTCTACACCGA[A/T]TAGTAGATTCAGTGC	4297
rs782576223	snp	A/C	1.64999e-05	0.00287222	synonymous-codon	KMT2A	GRCh38.p7	11:118504073	TGTTGATGATGGGAC[A/C]GAGAGTGATACTAGT	4297
rs782577251	snp	C/G/T	0.000128222	0.00800589	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118436465	CCGCCTCCCCGCCCC[C/G/T]CTGTGTTGTCGCCTC	4297
rs782577475	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118511212	CTAATGAGAGTATTG[A/C]TAGAGTAGAGATGTC	4297
rs782578101	snp	A/C	1.65345e-05	0.00287524	synonymous-codon	KMT2A	GRCh38.p7	11:118482456	GAAAAAAGTGGCTCC[A/C]CGCCCAAGTATCCCT	4297
rs782578668	snp	A/G	6.62712e-05	0.00575597	missense, intron-variant	KMT2A	GRCh38.p7	11:118473171	GTTTTTCTGCATCTG[A/G]TACCGCTGCTTCAGC	4297
rs782580553	snp	A/G	1.64743e-05	0.00287	missense	KMT2A	GRCh38.p7	11:118506396	GGACTGGAGCAGAAC[A/G]AGGCTTTATCCTCAG	4297
rs782581690	snp	A/G	1.64912e-05	0.00287147	synonymous-codon	KMT2A	GRCh38.p7	11:118480174	TCGTTGTTTTCCTAG[A/G]ATGAGAAAATGTCAG	4297
rs782582229	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118468492	TTTTGGGCTGTATCT[A/G]TAGTTTGAAATTAGG	4297
rs782582553	snp	C/T	1.65381e-05	0.00287555	missense	KMT2A	GRCh38.p7	11:118501079	CTCCAGTCGTAGAGC[C/T]GGATATCAACAGCAC	4297
rs782583649	snp	C/T	1.65979e-05	0.00288074	intron-variant	KMT2A	GRCh38.p7	11:118497906	TGGCATTATATTCTT[C/T]AGGAAAAAAGAAATC	4297
rs782585188	snp	A/C	1.65272e-05	0.0028746	missense	KMT2A	GRCh38.p7	11:118504099	CTAGTGTCACAGCCA[A/C]AACAAGGAAAAGCAG	4297
rs782585360	snp	C/G	1.64762e-05	0.00287016	missense	KMT2A	GRCh38.p7	11:118502994	TCTTCTAAAGAGGCC[C/G]TCTCCTTCCCACACC	4297
rs782585423	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118469776	CTTAGCTTGTGATGT[A/G]TGCTAGCATTAGGGT	4297
rs782585538	snp	A/G	1.65318e-05	0.002875	missense	KMT2A	GRCh38.p7	11:118478182	TTTGGTGGTCGCAAT[A/G]TAAAGAAGCAGTGCT	4297
rs782585584	snp	C/G	1.75965e-05	0.00296613	intron-variant	KMT2A	GRCh38.p7	11:118509924	ATTTGTTACTGCAAC[C/G]ACTATCTATTTTCTC	4297
rs782585877	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118457516	GACCTCATGATCCAC[A/C]TGCGTTGGCCTCCCA	4297
rs782587358	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118481223	TTGTACCCATTAACC[A/G]TCCCCACTTTCCCCC	4297
rs782589332	snp	G/T	1.64803e-05	0.00287052	missense	KMT2A	GRCh38.p7	11:118484199	AAAAACCACCTCCGG[G/T]CAATAAGCAGGAGAA	4297
rs782589960	snp	C/T	1.65168e-05	0.00287369	missense	KMT2A	GRCh38.p7	11:118501831	CAACACAGAGATCCC[C/T]TGGCTGTCGACCGTT	4297
rs782589998	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118494470	GAATACAATGAACTT[G/T]TTCTCTTCTACTTTT	4297
rs782591418	snp	G/T	1.65051e-05	0.00287267	synonymous-codon	KMT2A	GRCh38.p7	11:118506074	CCAGCAGAGCCTGGG[G/T]ATTCAGGACCAGCCT	4297
rs782591573	snp	A/G	0.000186978	0.00966716	intron-variant	KMT2A	GRCh38.p7	11:118498335	TTAAAACATATGAAA[A/G]TCTGAATAGGACTCT	4297
rs782591672	snp	C/T	1.84099e-05	0.00303391	intron-variant	KMT2A	GRCh38.p7	11:118509099	TTTGAATTGAAGAAC[C/T]AGCTGATATTATATC	4297
rs782591851	snp	A/C/T	3.3093e-05	0.00406763	missense, intron-variant	KMT2A	GRCh38.p7	11:118472645	CAGGCTTCTGAGGAG[A/C/T]TTCAGGTACTTCCTG	4297
rs782592821	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118454097	AAAACCTCAGACTCT[C/G]CCATTATAGTCTCTT	4297
rs782593902	snp	C/T	2.66237e-05	0.00364844	missense	KMT2A	GRCh38.p7	11:118436840	CTGCTCCGGGTGGGC[C/T]CGGGCTTCGACGCGG	4297
rs782594163	snp	G/T	1.64743e-05	0.00287	missense	KMT2A	GRCh38.p7	11:118491829	GCACCCTGCAGAGTG[G/T]CGACTGGCCCTTGAA	4297
rs782595300	snp	C/G	1.64751e-05	0.00287007	missense	KMT2A	GRCh38.p7	11:118504951	TAGAGCAAGGTCATG[C/G]CAACAATCAGGATTT	4297
rs782596170	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118484130	TTATCTGTTGCAAAT[A/G]TGAAGGCAAATAGGG	4297
rs782596303	snp	C/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512530	CCATATGTTGCTTAT[C/G]CATTCATTAGTCAGT	4297
rs782596360	snp	A/G	1.66299e-05	0.00288352	missense, intron-variant	KMT2A	GRCh38.p7	11:118471724	GACCGAAATTCAGCT[A/G]TCCTCTCAGATCCAT	4297
rs782596573	snp	A/G	0.000214145	0.0103454	missense	KMT2A	GRCh38.p7	11:118506267	CAGCTTCAGCATGTG[A/G]ACCAGCTCCTTGCCA	4297
rs782597627	snp	A/T	1.78908e-05	0.00299084	intron-variant	KMT2A	GRCh38.p7	11:118481696	ATAGACAGATGATGT[A/T]GTTGTGTTTTTCCCT	4297
rs782597910	in-del	-/T	3.30816e-05	0.00406691	intron-variant	KMT2A	GRCh38.p7	11:118468871	TAAGTGCATGGTGCC[-/T]TTTAAGTTTTGTTTG	4297
rs782600332	snp	G/T	1.6473e-05	0.00286988	missense, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521354	TGAGATGGTGATTGA[G/T]TATGCCGGCAACGTC	4297
rs782600535	snp	A/C/T	3.29458e-05	0.00405857	missense	KMT2A	GRCh38.p7	11:118505799	TATTTTGAACCGGCA[A/C/T]CCCTGTTACCACAGA	4297
rs782600770	snp	A/G	1.65397e-05	0.00287569	missense	KMT2A	GRCh38.p7	11:118503187	ATAGGAGACAGAAAG[A/G]GAAAAAATCCTGTAA	4297
rs782600875	snp	G/T	4.20495e-05	0.00458508	synonymous-codon	KMT2A	GRCh38.p7	11:118436728	GGGAAGCAGCGGGGC[G/T]GGGGTTCCAGGGGGA	4297
rs782601484	snp	C/T	1.64757e-05	0.00287012	missense	KMT2A	GRCh38.p7	11:118501725	ATAAGTCCTCCATCA[C/T]CAGACCGACCTCCTC	4297
rs782602225	snp	C/G	1.65323e-05	0.00287505	missense	KMT2A	GRCh38.p7	11:118507569	CAGGATACAGCTAGC[C/G]TGGAGCAGTCCTCCC	4297
rs782603046	snp	A/T	3.29511e-05	0.00405887	synonymous-codon	KMT2A	GRCh38.p7	11:118504721	CACCCGGAGTCCCAC[A/T]GTCCCCAGCCAGAAT	4297
rs782603151	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118475795	CTAATTCTGCCAGTT[C/G]AGAATTGTAGCAGGA	4297
rs782603194	in-del	-/AAAGA			intron-variant	KMT2A	GRCh38.p7	11:118446358	GTCTCAAAAGAAAGA[-/AAAGA]AAAGAAAAGAAAAGA	4297
rs782603430	snp	G/T	1.8069e-05	0.00300569	intron-variant	KMT2A	GRCh38.p7	11:118488790	AATAGAACTACAGCT[G/T]GGCCTCTGTATCAGT	4297
rs782603477	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118440136	GGTTCGCCTTCAGTG[A/C]ATAATGACTATAACT	4297
rs782604149	snp	C/G	1.648e-05	0.0028705	missense, intron-variant	KMT2A	GRCh38.p7	11:118474048	CAAAATACTTATAAA[C/G]AAAGGGAGAGGAAAT	4297
rs782604487	snp	A/G	1.66751e-05	0.00288744	missense	KMT2A	GRCh38.p7	11:118482030	CAGGACCGCCAAGAA[A/G]AGAAGTTCCCAAAAC	4297
rs782604997	snp	C/T	7.90045e-05	0.00628459	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118434905	GCTCTGCACAAATGT[C/T]TCGCCAGTGGAGGGA	4297
rs782605513	snp	A/G	3.29766e-05	0.00406045	missense	KMT2A	GRCh38.p7	11:118468778	CCTTTGTTGTAGGAT[A/G]AGCAATTCTTAGGTT	4297
rs782605777	snp	A/G	1.65425e-05	0.00287593	missense	KMT2A	GRCh38.p7	11:118502776	AAATGAAGCAGTCCA[A/G]TGCTTCAGACTTGGT	4297
rs782607124	snp	A/G			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118524341	TGGAAGTCTAGCAAA[A/G]CAATACGACTCAGCC	4297
rs782607680	in-del	-/TCC			intron-variant	KMT2A	GRCh38.p7	11:118489964	CTTGTATTACAAATA[-/TCC]TCTATGCTTGAGGAT	4297
rs782607956	snp	C/T	3.30398e-05	0.00406434	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118472464	GGATGAGGATTATGA[C/T]CCTCCAATTAAAATT	4297
rs782607990	in-del	-/C			intron-variant	KMT2A	GRCh38.p7	11:118437812	AAAATAGTCCACTGT[-/C]CCCTAGGCTTAGAGA	4297
rs782608062	snp	A/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118516036	CCAGGATTGTCTTAG[A/T]TTAATCATCTGGGGT	4297
rs782608459	snp	A/G	6.59055e-05	0.00574007	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473004	TATTTTGCGAGAACC[A/G]ACATTTAGGTGGACT	4297
rs782608868	snp	C/T	1.65151e-05	0.00287355	missense	KMT2A	GRCh38.p7	11:118504173	TTAAAGATTGATAGA[C/T]CTGAAGATGCTGGGG	4297
rs782610110	snp	A/G			missense	KMT2A	GRCh38.p7	11:118504485	ACTCCATCCATGCAG[A/G]CTTTGGGTGAGAGCC	4297
rs782610117	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118454348	CTGCTATATAGCCAC[A/G]CTAGCCTTTTTCTGT	4297
rs782610565	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118440592	CTTCACAAAATATTA[A/C]AAGCAAAATTTCCAT	4297
rs782611606	snp	A/C/G	6.81435e-05	0.00583676	intron-variant	KMT2A	GRCh38.p7	11:118489935	AACCACCATGTGACT[A/C/G]TTGGACTTATGTAAC	4297
rs782612820	snp	C/T	1.80211e-05	0.0030017	intron-variant	KMT2A	GRCh38.p7	11:118490286	GCCAGCTTTCGGAGG[C/T]TGTACTTGGTGTTCT	4297
rs782612837	in-del	-/CC	1.67428e-05	0.00289329	intron-variant	KMT2A	GRCh38.p7	11:118489915	ATGATGCTCTTTTAT[-/CC]AGAGAACCACCATGT	4297
rs782613036	snp	A/C/G	6.96403e-05	0.00590045	intron-variant	KMT2A	GRCh38.p7	11:118488445	CTCTGAATCTCCCGC[A/C/G]GTGTCCAATACTGTA	4297
rs782613318	snp	G/T	0.00244039	0.0348459	intron-variant, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512040	GGTAATGGCTGGAGG[G/T]GTTATTCCACTCCTG	4297
rs782614384	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118452811	GCTAATTTTTGTATT[C/T]TTAGTAGAGATGGGG	4297
rs782614654	snp	C/T	3.29739e-05	0.00406028	missense, intron-variant	KMT2A	GRCh38.p7	11:118472784	GTTTTGGATCTAGAA[C/T]GACGAAAAAATTATC	4297
rs782615088	snp	A/G	1.64765e-05	0.00287019	synonymous-codon	KMT2A	GRCh38.p7	11:118503335	TATGGGCCAACGACC[A/G]TGTAACAATGTTTCT	4297
rs782616287	snp	C/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118518489	ATTGCTTTTAAACTT[C/T]AGTGAGGCTGGCTGG	4297
rs782617059	snp	C/G	1.73893e-05	0.00294862	missense	KMT2A	GRCh38.p7	11:118506630	CAAGAAACGACATCC[C/G]TGACCTCAGGCACAG	4297
rs782617745	snp	A/C			missense	KMT2A	GRCh38.p7	11:118503406	TCCCCAAAGCTCCAC[A/C]CATGCAAGTAGAAGG	4297
rs782619122	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118457438	CGCCTGGCTAATTTT[C/T]TTTTTGTATTTTTTA	4297
rs782621411	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118459358	AGGTGTGAGCCACCA[C/T]GCCAGGCCCTGATTT	4297
rs782621598	snp	C/T	1.66969e-05	0.00288932	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118472239	TAAGCCAGTTAGGAT[C/T]ATTCCTTCTTCAAAA	4297
rs782621668	snp	A/G	1.68388e-05	0.00290158	synonymous-codon	KMT2A	GRCh38.p7	11:118510117	TGCAGAAAGTATTGA[A/G]GGTGAGTGGATTAAA	4297
rs782621928	snp	C/G	5.74564e-05	0.00535956	utr-variant-5-prime	KMT2A	GRCh38.p7	11:118436504	GCTGCTTCACTTCAC[C/G]GGGCGAACATGGCGC	4297
rs782622119	snp	A/T	0.000141173	0.0084004	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118434696	CCCACCCTTTTAGCA[A/T]CTAGTAAACCACGCG	4297
rs782622722	snp	C/T	1.77351e-05	0.00297779	intron-variant	KMT2A	GRCh38.p7	11:118509910	AGTGCTCAGTGAGCA[C/T]TTGTTACTGCAACCA	4297
rs782623345	snp	A/G	2.00918e-05	0.00316946	intron-variant	KMT2A	GRCh38.p7	11:118494266	GTTTTAAGAATAATT[A/G]ACATTTTGTTTTTGT	4297
rs782623689	snp	C/G	1.64942e-05	0.00287173	missense, intron-variant	KMT2A	GRCh38.p7	11:118473564	CTTTTCCTTCTCATT[C/G]CCTGACTCAGTCTGG	4297
rs782625001	snp	A/C	3.44602e-05	0.00415077	missense	KMT2A	GRCh38.p7	11:118506622	TTCCAGACCAAGAAA[A/C]GACATCCCTGACCTC	4297
rs782626212	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118501910	CAGCCCAAAGACTAA[C/T]TTGTAATTCTTTCAG	4297
rs782627212	snp	A/T	1.64732e-05	0.0028699	synonymous-codon	KMT2A	GRCh38.p7	11:118506296	CAGCAAAACTGGGAT[A/T]CATTCTTCCCAGCGT	4297
rs782627272	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118511077	TTCAGTGCCAAACCT[G/T]GAGGACTTTGAAAAC	4297
rs782627566	snp	A/G	1.64741e-05	0.00286998	synonymous-codon	KMT2A	GRCh38.p7	11:118497953	TGCTGGTCGTTTACT[A/G]TATATTGGCCAAAAT	4297
rs782627776	snp	A/G	1.64819e-05	0.00287066	missense	KMT2A	GRCh38.p7	11:118506174	ATAACAGCGGCATCT[A/G]GCATCTGTGTGCTCC	4297
rs782628184	snp	A/G	1.67489e-05	0.00289381	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522196	TTCTCCCCCAGTGTT[A/G]GAGTGCAAGGAGGCG	4297
rs782629027	in-del	-/G			intron-variant	KMT2A	GRCh38.p7	11:118482838	CAGGAGGCTGAGATA[-/G]GAAGGATTGTCTTGA	4297
rs782629519	snp	A/G	1.65272e-05	0.0028746	synonymous-codon	KMT2A	GRCh38.p7	11:118502708	AAATTTGCAAAGGAC[A/G]GTGGTTACTGTAGGC	4297
rs782629582	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118443420	ACCTTGTCAGGTTAC[A/G]CACCAGGGGAAGCCA	4297
rs782629999	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118450861	GAATTTCATTAACTA[G/T]TTGGCTTAAGAAGTT	4297
rs782630016	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118441912	CTCACCTTAGAGCTG[C/T]CCTTCCGTGGGGCAG	4297
rs782630604	snp	A/C/G	3.36946e-05	0.00410443	intron-variant	KMT2A	GRCh38.p7	11:118476769	ATAATTTCAACATGT[A/C/G]TGGTTGTTATTGTTT	4297
rs782630630	snp	A/G	1.65658e-05	0.00287795	intron-variant	KMT2A	GRCh38.p7	11:118499792	CAAAAAAATAAAATG[A/G]CGCTCATAATCTTCT	4297
rs782630773	snp	C/T			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522907	TTTTCTTCCTTTCCC[C/T]TGTCTTCATGCCACT	4297
rs782631753	snp	A/C/T	8.23708e-05	0.00641712	missense	KMT2A	GRCh38.p7	11:118505605	AGAATAAAAAACTTG[A/C/T]TCCCTCTAGTACCCC	4297
rs782633253	snp	A/G	1.6513e-05	0.00287336	missense	KMT2A	GRCh38.p7	11:118501687	AAAGTTCATCAAAAG[A/G]GAGTCAAAACACAGC	4297
rs782634628	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118455845	TGAGACTACACCACA[C/T]CCAGCTAATTTTTGT	4297
rs782635067	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118486844	AGTGAGCCATTATCA[C/T]GCCACTGCACTCCAG	4297
rs782635734	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520290	GTTTTCTTTAATGAT[A/G]GTATACTCTGTCAGC	4297
rs782636439	snp	C/T	1.65381e-05	0.00287555	intron-variant	KMT2A	GRCh38.p7	11:118499947	AGAAGAGAGCAGCCC[C/T]ACAACCTGAACACAC	4297
rs782636717	snp	C/T	1.64762e-05	0.00287016	missense	KMT2A	GRCh38.p7	11:118506525	AAACCAAAAACCAAA[C/T]GGTTTCAGCTGCCTC	4297
rs782637506	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118479866	AGAGTAGGACTGATG[C/T]GACTACAAGAAATAC	4297
rs782637744	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118507879	GAGGCAGGAGAAGGG[A/C]GTGAACCCAGGAGGC	4297
rs782638304	in-del	-/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512803	CTTACCTGTTTTTTG[-/T]TTTTTTTTTTTTTAT	4297
rs782638615	snp	C/T	1.64852e-05	0.00287094	synonymous-codon	KMT2A	GRCh38.p7	11:118502486	TGGCTCCAGGCGTCA[C/T]AGTACCTCTTCCTTA	4297
rs782638810	snp	A/G	1.64904e-05	0.00287139	missense	KMT2A	GRCh38.p7	11:118506033	CCAGATATTGGCTCA[A/G]TAAGCAATCTTTTAA	4297
rs782639068	snp	G/T	1.64798e-05	0.00287047	missense	KMT2A	GRCh38.p7	11:118502893	CTGGAATTCCTAAAC[G/T]GGCCCCACAGGTTCA	4297
rs782639231	snp	C/T	1.6477e-05	0.00287024	missense	KMT2A	GRCh38.p7	11:118505179	TTTATGTTCTCCAAA[C/T]TCTTCCAAATGGAGT	4297
rs782639582	snp	A/G	0.00647333	0.0565222	intron-variant	KMT2A	GRCh38.p7	11:118439148	TTTGCTTTTTTAAAA[A/G]ATACAGCAGCAAAAA	4297
rs782639799	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118471301	TGGTGGCTAGGATAT[A/G]GCGAGGAAGTTCAGA	4297
rs782640359	snp	G/T	1.6477e-05	0.00287024	missense	KMT2A	GRCh38.p7	11:118504926	ATCTCTAGCCCTCCT[G/T]GTGGTTCAGTAGAGC	4297
rs782640926	snp	A/G	1.67379e-05	0.00289287	missense, intron-variant	KMT2A	GRCh38.p7	11:118473761	GATGCTGACAAGAGC[A/G]TGGAGAAGGACAAGA	4297
rs782641177	snp	C/T	9.88549e-05	0.00702977	missense	KMT2A	GRCh38.p7	11:118505458	CTTCAGGCCTGCTTA[C/T]TGGGGTTCAGCCTCC	4297
rs782644725	snp	C/T	1.65173e-05	0.00287374	synonymous-codon	KMT2A	GRCh38.p7	11:118504088	AGAGAGTGATACTAG[C/T]GTCACAGCCACAACA	4297
rs782645001	snp	C/G			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118523675	AATTTAAAAGAAGAT[C/G]GGTTTTTAATAATTT	4297
rs782645802	snp	A/C	0.000131885	0.00811942	missense	KMT2A	GRCh38.p7	11:118504344	GTCCACACAAGTACC[A/C]CCTCCGACAAAAATT	4297
rs782646508	snp	C/T	1.64898e-05	0.00287135	missense, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521931	TCCGAATTGATGACT[C/T]AGAGGTAGTGGATGC	4297
rs782646794	snp	A/G	1.64776e-05	0.00287028	missense	KMT2A	GRCh38.p7	11:118484211	CGGTCAATAAGCAGG[A/G]GAATGCAGGCACTTT	4297
rs782647276	snp	A/G			missense	KMT2A	GRCh38.p7	11:118481888	AAGCCCGTCGAGGAA[A/G]AGAGTGAAGAAGGGA	4297
rs782647777	snp	C/T	8.27506e-05	0.00643183	missense, intron-variant	KMT2A	GRCh38.p7	11:118471775	AAATCAGAGACCAAA[C/T]CTGGAGATAAGATCA	4297
rs782649329	snp	C/T	1.64909e-05	0.00287144	missense	KMT2A	GRCh38.p7	11:118484946	CCCAGGGTGGTTTGC[C/T]TTCTCTGTGCCAGTA	4297
rs782649425	snp	C/T	1.64855e-05	0.00287097	intron-variant	KMT2A	GRCh38.p7	11:118488586	ATATTATTTGACATA[C/T]TTCTATCTTCCCATG	4297
rs782651115	snp	C/G	1.64808e-05	0.00287057	missense	KMT2A	GRCh38.p7	11:118480209	TACAATGGATGCCTT[C/G]CAAAGCCTACCTGCA	4297
rs782651251	snp	A/T			missense, intron-variant	KMT2A	GRCh38.p7	11:118473650	CCATTTTCATCAAGT[A/T]GTCCTACTCCTCTCT	4297
rs782651889	snp	A/G	1.64735e-05	0.00286993	missense, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521320	GGGGTCTTTTCTGTA[A/G]GAGAAACATTGATGC	4297
rs782653043	snp	C/T	1.64735e-05	0.00286993	missense, intron-variant	KMT2A	GRCh38.p7	11:118472955	CACCATTTTTGCCTG[C/T]TTCCACTGCTCCTAT	4297
rs782653173	in-del	-/T			intron-variant	KMT2A	GRCh38.p7	11:118441915	ACCTTAGAGCTGTCC[-/T]TCCGTGGGGCAGCTG	4297
rs782653473	snp	C/T	1.65203e-05	0.002874	intron-variant	KMT2A	GRCh38.p7	11:118493252	TTCTACAGTGAGCCA[C/T]CAGAATTTCTAGTGC	4297
rs782653687	snp	A/G	3.30967e-05	0.00406783	intron-variant	KMT2A	GRCh38.p7	11:118493270	GAATTTCTAGTGCCA[A/G]TAAAGCTTCTTTGGA	4297
rs782653706	snp	A/G/T	9.3691e-05	0.00684384	missense	KMT2A	GRCh38.p7	11:118436742	CTGGGGTTCCAGGGG[A/G/T]AGCGGCCGCCGCCTC	4297
rs782653794	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118456529	GTTTTTAGTAGAGAT[C/G]GGGTTTCACTATGTT	4297
rs782653980	snp	A/C	1.67615e-05	0.0028949	intron-variant	KMT2A	GRCh38.p7	11:118491365	TCTAGGTACTACTAC[A/C]TTTATTAGCCTCTAG	4297
rs782655113	snp	A/C	1.64787e-05	0.00287038	missense	KMT2A	GRCh38.p7	11:118503009	CTCTCCTTCCCACAC[A/C]TCCATTTGAGAGGGC	4297
rs782655826	snp	C/T	3.46081e-05	0.00415967	intron-variant	KMT2A	GRCh38.p7	11:118494795	AGCATAACTTTTTTT[C/T]CTCCTCATCGGCTAG	4297
rs782656966	snp	A/G	3.29766e-05	0.00406045	synonymous-codon	KMT2A	GRCh38.p7	11:118468783	GTTGTAGGATGAGCA[A/G]TTCTTAGGTTTTGGC	4297
rs782657563	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118514880	TCAGGTAATCTGCCC[A/G]CCTCAGCCTCCCAAA	4297
rs782657698	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118463575	ACTTTAGACAACTTA[C/T]TCAATTCCTTTAAAT	4297
rs782658526	in-del	-/T	0.00414077	0.0453127	intron-variant	KMT2A	GRCh38.p7	11:118438989	TGCTGTAGATTATTA[-/T]TTTTTTTTGAAAGGC	4297
rs782658611	snp	A/G	1.6473e-05	0.00286988	missense, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519699	CTGGTGCCAAGCACT[A/G]TCGAAATTACAAATT	4297
rs782659759	snp	A/C/G	3.29849e-05	0.00406098	synonymous-codon, missense, intron-variant	KMT2A	GRCh38.p7	11:118473442	GACAAGAAGTGGAAG[A/C/G]CTTAGTAGTTCTGAG	4297
rs782660217	snp	C/G	1.64882e-05	0.00287121	missense, intron-variant	KMT2A	GRCh38.p7	11:118472814	CAACTCTACAAAGTG[C/G]CCCCCAGCAGCAGAC	4297
rs782660276	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118454190	CTGGTATCAAATCCT[A/G]TTCCTTCACTTTAAA	4297
rs782661362	snp	C/T	1.6516e-05	0.00287362	synonymous-codon	KMT2A	GRCh38.p7	11:118506566	GAATGGCAAGAAGCA[C/T]AAAGTTTCCCATTTG	4297
rs782661653	snp	A/G	3.29647e-05	0.00405971	missense	KMT2A	GRCh38.p7	11:118503810	ACCCCACTCTATGGA[A/G]TAAGATCCTATGGTG	4297
rs782661777	snp	A/G	1.65293e-05	0.00287479	missense	KMT2A	GRCh38.p7	11:118507558	AGGCTGAGCAGCAGG[A/G]TACAGCTAGCGTGGA	4297
rs782662091	snp	G/T	1.64885e-05	0.00287123	missense, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512022	AAGCAGCTCTCATTT[G/T]CAGGTAATGGCTGGA	4297
rs782663689	snp	A/G	4.94866e-05	0.00497402	missense	KMT2A	GRCh38.p7	11:118499903	GATAAGCTCTTTCCT[A/G]TTGGATATCAGTAAG	4297
rs782663858	snp	A/C	1.648e-05	0.0028705	missense, intron-variant	KMT2A	GRCh38.p7	11:118474074	GAAATCTGGAAAAAA[A/C]CAACTTGGACCTCGG	4297
rs782664456	snp	A/G			missense	KMT2A	GRCh38.p7	11:118491235	AATGTTATGATGATG[A/G]TGACTATGAGAGTAA	4297
rs782664461	snp	G/T	1.80478e-05	0.00300392	intron-variant	KMT2A	GRCh38.p7	11:118481691	TCACTATAGACAGAT[G/T]ATGTTGTTGTGTTTT	4297
rs782665441	snp	C/G/T	1.64798e-05	0.00287047	synonymous-codon, missense	KMT2A	GRCh38.p7	11:118503936	TCAGATGAAGACGAC[C/G/T]TATACTATTACAACT	4297
rs782665690	snp	C/T	3.33045e-05	0.00408058	missense	KMT2A	GRCh38.p7	11:118495864	CAGACTCACCAACTC[C/T]TCTGCATCCTCCTAC	4297
rs782665766	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118510789	TACTAGAAGAGTTCA[A/T]AGAAGAGAAAGGTCA	4297
rs782665812	snp	C/T	1.65332e-05	0.00287512	intron-variant	KMT2A	GRCh38.p7	11:118498112	ATGAAAGAGATTCCC[C/T]CTCAGTTTCCAGATA	4297
rs782666041	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118498974	CACATAGTTGGAATC[A/C]TATAGTACATAGCCT	4297
rs782666181	snp	G/T	3.30235e-05	0.00406333	missense	KMT2A	GRCh38.p7	11:118501058	GCAAGATAGTGGAGT[G/T]CCGTCCTCCAGTCGT	4297
rs782666540	snp	A/T	1.64838e-05	0.00287083	synonymous-codon	KMT2A	GRCh38.p7	11:118501709	AAACACAGCTGAAAT[A/T]ATAAGTCCTCCATCA	4297
rs782667443	snp	C/G	0.000115315	0.00759236	missense	KMT2A	GRCh38.p7	11:118506426	GCTGTGCAAGCCAGC[C/G]CCACCTCTCCTGGGG	4297
rs782667502	snp	A/G	3.30262e-05	0.0040635	missense, intron-variant	KMT2A	GRCh38.p7	11:118473608	AAAAATCAGAGACCA[A/G]GGAAGCAGACTAGTG	4297
rs782669019	snp	A/G	4.94336e-05	0.00497135	synonymous-codon	KMT2A	GRCh38.p7	11:118503548	TGCTTCCCCTTTGCA[A/G]ATAGAGTCAACATCT	4297
rs782669151	snp	A/G	1.66546e-05	0.00288566	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520769	ACATTATTTCCTGAA[A/G]AAAATTCGTTAATAG	4297
rs782669781	snp	A/G	1.64738e-05	0.00286995	missense	KMT2A	GRCh38.p7	11:118505964	ACAACCCCTACAAGT[A/G]GTGCGTCAGTTCCAG	4297
rs782670336	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118442075	GGTCTCCTAATTAAG[A/T]TCTCTTTGTGCCTGC	4297
rs782670360	snp	A/G	4.94189e-05	0.00497062	missense	KMT2A	GRCh38.p7	11:118506310	TTCATTCTTCCCAGC[A/G]TGATCTTGATTCTGC	4297
rs782670845	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118445123	GTATATGTATGCATA[C/T]ATACACCTATTTGAG	4297
rs782672091	snp	C/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512390	TCAGACAATATGTAG[C/T]CTTTTGTGACCGTCT	4297
rs782672328	snp	C/T	1.6477e-05	0.00287024	missense	KMT2A	GRCh38.p7	11:118502559	ACTGGGAATACTTAC[C/T]CTAGGAATAATGTTT	4297
rs782673356	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118446705	GTTTATTGTGGTAAT[C/T]TTCTCATTGGTCTTC	4297
rs782673496	snp	C/T			utr-variant-3-prime, intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118525109	GAAAGAAGGCAAAAA[C/T]GGCACAGCTATCTCC	4297
rs782673676	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118479199	GTCTTATTCATTCTT[G/T]CTGATTATTTTTTTG	4297
rs782673964	snp	C/T	1.64741e-05	0.00286998	missense	KMT2A	GRCh38.p7	11:118506289	TCCTTGCCAGCAAAA[C/T]TGGGATTCATTCTTC	4297
rs782674872	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118452694	GCTGGAGTGCAGTGG[C/T]GCCATCTCGGCTCAC	4297
rs782675040	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118518063	AATTGCATATGTGCA[A/G]TTGCAGTCCTAATAC	4297
rs782675095	snp	A/G	1.64738e-05	0.00286995	missense, intron-variant	KMT2A	GRCh38.p7	11:118473908	TCCAAAGAGAAGGTT[A/G]TTGGTGAAGATGTTG	4297
rs782675548	snp	A/G	1.6832e-05	0.00290099	intron-variant	KMT2A	GRCh38.p7	11:118501865	TTCTGCAGGTAAAAG[A/G]CTTTATTGACCTACT	4297
rs782675823	snp	A/G	1.64749e-05	0.00287005	missense	KMT2A	GRCh38.p7	11:118505136	GCCACTGAGAAACTC[A/G]TAGTTGTTAACCAGA	4297
rs782676153	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118481406	GTCCTCTAGTTCCAT[C/T]CATGTTGTTTCAGAT	4297
rs782676585	snp	C/T	1.65348e-05	0.00287526	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473139	ACTAACTCCCGAGGA[C/T]GTTGGCTTTGCATCT	4297
rs782677148	snp	A/G	1.65748e-05	0.00287874	intron-variant	KMT2A	GRCh38.p7	11:118484330	GTAAAGGTGTTCAGT[A/G]ATCATAAAGTATATT	4297
rs782677378	snp	G/T			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522804	TGCAGGCTTTGAGTG[G/T]GAGTGTTGCCCCCAG	4297
rs782677866	snp	G/T	1.6476e-05	0.00287014	missense	KMT2A	GRCh38.p7	11:118503579	CCCACAGAACCAATT[G/T]CAGCCTCTGAAAATC	4297
rs782678655	snp	A/G	1.70304e-05	0.00291803	missense	KMT2A	GRCh38.p7	11:118506612	GAAGCACACATTCCA[A/G]ACCAAGAAACGACAT	4297
rs782678769	snp	A/T	1.68798e-05	0.0029051	intron-variant	KMT2A	GRCh38.p7	11:118476758	TTCGTTCAGTTATAA[A/T]TTCAACATGTATGGT	4297
rs782678915	snp	C/G	1.67649e-05	0.0028952	intron-variant	KMT2A	GRCh38.p7	11:118493010	AATTTACATGGACAC[C/G]TTGGTTTTAGTGTTA	4297
rs782679150	snp	A/G	1.64966e-05	0.00287194	missense	KMT2A	GRCh38.p7	11:118505295	GGTGGTCTCACCCTT[A/G]CCACAGGACTAAATC	4297
rs782680161	snp	C/G	3.29484e-05	0.00405871	missense	KMT2A	GRCh38.p7	11:118478137	CCTGAGGACTGTGGT[C/G]TTTGTACTAATTGCT	4297
rs782682980	snp	A/C	6.58903e-05	0.00573941	missense	KMT2A	GRCh38.p7	11:118505808	CCGGCACCCCTGTTA[A/C]CACAGAGTGTGGGAG	4297
rs782683534	snp	A/G	1.65239e-05	0.00287431	missense	KMT2A	GRCh38.p7	11:118481871	GTGAGCCTCCTCCAC[A/G]AAAGCCCGTCGAGGA	4297
rs782685419	snp	C/T	3.33801e-05	0.00408521	utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522189	GCTGCTCTTCTCCCC[C/T]AGTGTTGGAGTGCAA	4297
rs782685497	snp	A/G	1.67486e-05	0.00289379	intron-variant	KMT2A	GRCh38.p7	11:118489918	GATGCTCTTTTATAG[A/G]GAACCACCATGTGAC	4297
rs782685611	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118484828	AAGTTGTGTAATTGT[A/G]AAACTTTCCTAAGTG	4297
rs782685763	snp	C/T	1.64836e-05	0.0028708	synonymous-codon	KMT2A	GRCh38.p7	11:118476831	TGACTCATCAGAGAC[C/T]TCTGTGCGAGGACCC	4297
rs782686356	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118491140	TGCAAGTCGAGGGCC[A/G]TAAAAACACGGGTAT	4297
rs782686359	snp	A/C/T	3.52313e-05	0.00419698	intron-variant	KMT2A	GRCh38.p7	11:118485011	GTACCCCAGGAAGTA[A/C/T]ATAAATTATTTTTCT	4297
rs782686435	snp	C/T	6.59576e-05	0.00574234	synonymous-codon, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520814	TAGGAGGGCAACTAG[C/T]ATGGATCTGCCAATG	4297
rs782686740	snp	A/C/G	4.88714e-05	0.00494305	synonymous-codon	KMT2A	GRCh38.p7	11:118436827	TTCAGGGCCGGCCCT[A/C/G]CTCCGGGTGGGCCCG	4297
rs782687082	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118440340	CACTGTAAGAAATCA[A/G]AGGTCCATTTTTTGC	4297
rs782689014	snp	A/T	1.65436e-05	0.00287602	missense	KMT2A	GRCh38.p7	11:118502764	CTTCATCTTCAGAAA[A/T]GAAGCAGTCCAGTGC	4297
rs782689864	snp	A/G	1.64757e-05	0.00287012	missense	KMT2A	GRCh38.p7	11:118502955	AAAATCGGCTCCTTT[A/G]CTGAACCCTCTTCAG	4297
rs782690725	snp	C/G	1.64746e-05	0.00287002	missense	KMT2A	GRCh38.p7	11:118505586	TCTCGTCTACAGACC[C/G]GAAAGAATAAAAAAC	4297
rs782691048	snp	A/G	1.66299e-05	0.00288352	synonymous-codon	KMT2A	GRCh38.p7	11:118482016	TCAGCCACCTACTAC[A/G]GGACCGCCAAGAAAA	4297
rs782691915	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118497048	TCGCTCTTGTTGCCC[A/G]GGCTGGAGTGCAATG	4297
rs782692901	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118446006	AAGACTCTGTCTCCA[A/G]AAAAAAGAAAGAAAA	4297
rs782694778	snp	A/G	1.65135e-05	0.00287341	missense	KMT2A	GRCh38.p7	11:118504176	AAGATTGATAGACCT[A/G]AAGATGCTGGGGAGA	4297
rs782695422	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118490720	AATAATATAGGAGAT[C/G]TCTGTATATAAAGAA	4297
rs782696375	snp	C/T	1.65718e-05	0.00287848	intron-variant	KMT2A	GRCh38.p7	11:118493046	AAGCAACATATCTTT[C/T]CTGGCAATAGGCTGC	4297
rs782696657	snp	A/G	3.29538e-05	0.00405904	missense	KMT2A	GRCh38.p7	11:118502902	CTAAACTGGCCCCAC[A/G]GGTTCATAACACAAC	4297
rs782697858	snp	C/T	1.64789e-05	0.0028704	synonymous-codon	KMT2A	GRCh38.p7	11:118506227	AACAGCCGCTTCACC[C/T]TCTGGGGAAGCAGAC	4297
rs782698036	snp	A/G	1.66771e-05	0.00288761	intron-variant	KMT2A	GRCh38.p7	11:118482530	TCTGCCATTTCTCAG[A/G]GATGTATTCTATTTT	4297
rs782698697	snp	A/C	3.61723e-05	0.00425262	intron-variant	KMT2A	GRCh38.p7	11:118502389	TATTACTTTTTCTCT[A/C]TTGTTTAGGAAGTCC	4297
rs782698989	snp	C/T	3.29451e-05	0.00405851	missense	KMT2A	GRCh38.p7	11:118505884	CTAGCCACCTCACAT[C/T]AGGGTCTGTGTCTGG	4297
rs782699097	snp	A/C	1.66294e-05	0.00288347	synonymous-codon	KMT2A	GRCh38.p7	11:118498519	ACATCGGGATTTGAT[A/C]AAAGGCGAAGTGAGA	4297
rs782699596	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118458293	CACTATGTTGGTCTA[G/T]AACTAGGCTGGTCTA	4297
rs782699640	snp	C/G	1.64754e-05	0.00287009	missense	KMT2A	GRCh38.p7	11:118504575	CGTGAAAAAGACATG[C/G]GTCTTTTTGAAGTAT	4297
rs782699755	snp	A/G	0.000359777	0.0134074	missense	KMT2A	GRCh38.p7	11:118436696	CCCCCGGCTGTGGCG[A/G]CCGCGGCGGCGGCGG	4297
rs782700054	snp	A/T	1.6498e-05	0.00287206	synonymous-codon, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118511970	CTGGAAGTCATTGAC[A/T]GATAAAGTCCAGGAA	4297
rs782700081	snp	A/G	4.94776e-05	0.00497357	synonymous-codon	KMT2A	GRCh38.p7	11:118491763	GATGTATGAGATTCT[A/G]TCTAATCTGCCAGAA	4297
rs782700266	snp	C/T	2.81345e-05	0.00375053	intron-variant, missense	KMT2A	GRCh38.p7	11:118439087	GACAAAAAGACTGAA[C/T]CGTTCAGGTTACTTG	4297
rs782701399	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118438693	AGGGGAGGGAGGAGA[C/T]CCCAAGGACCCTGGC	4297
rs782702303	snp	C/G	1.64749e-05	0.00287005	missense	KMT2A	GRCh38.p7	11:118505738	TAATACTTCATCTCA[C/G]CGAACTGTCCCCAAC	4297
rs782702702	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118452112	ACAGGCATAATCATC[A/G]TGTATTACAGACTTG	4297
rs782702779	snp	G/T	1.64996e-05	0.0028722	intron-variant	KMT2A	GRCh38.p7	11:118480275	TCCCCCAAATGCTCC[G/T]TGCTTAAATGGTGTA	4297
rs782704160	snp	A/C	1.64727e-05	0.00286986	missense	KMT2A	GRCh38.p7	11:118478053	ACTAGAAACAAGGCA[A/C]CCCAGGAACCTCCAG	4297
rs782704291	snp	A/T			missense	KMT2A	GRCh38.p7	11:118505691	CCCTCCCAGCTTCCT[A/T]ATCATCCAAGTCTGT	4297
rs782705469	snp	A/G	1.64879e-05	0.00287118	missense	KMT2A	GRCh38.p7	11:118504324	CATTGGAGTCAAGCC[A/G]CAGAGTCCACACAAG	4297
rs782705773	snp	A/T	1.65078e-05	0.00287291	missense	KMT2A	GRCh38.p7	11:118484304	TCCACAGGATCAGAG[A/T]GGACTTTAAGGTAAA	4297
rs782706061	snp	A/G	3.30338e-05	0.00406397	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118472716	CATTTCCCAGTCCCC[A/G]GAAAATGAGAGTAAT	4297
rs782707093	snp	A/G	1.6495e-05	0.0028718	intron-variant, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521275	TCTGACCTCTTTTCC[A/G]TCTTTGTCCTAGGTC	4297
rs782707495	snp	A/C	3.30371e-05	0.00406417	missense	KMT2A	GRCh38.p7	11:118502685	GGGCAAAACACTTCC[A/C]CCTCTTCAAATTTGC	4297
rs782711000	snp	A/G	1.65162e-05	0.00287365	missense	KMT2A	GRCh38.p7	11:118481826	CTACCCCATCAGCAA[A/G]AGAGGATCCTGCCCC	4297
rs782711321	snp	C/T	4.94605e-05	0.0049727	synonymous-codon	KMT2A	GRCh38.p7	11:118489830	CCGAAACAGCTATCA[C/T]CCTGAGTGCCTGGGA	4297
rs782711341	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118466579	CCAGCACTTTGGGAA[A/G]CCAAGGTGGGTGGAT	4297
rs782711809	snp	C/G	1.65488e-05	0.00287647	missense, intron-variant	KMT2A	GRCh38.p7	11:118472592	CTTCAGACTCCTCTC[C/G]ATCTAGTAGCCCCAG	4297
rs782711965	snp	C/T	1.65269e-05	0.00287457	missense	KMT2A	GRCh38.p7	11:118503238	ATTCCAGTAAATCTT[C/T]TTTGGAACCTGGTCA	4297
rs782712242	snp	C/T	1.65389e-05	0.00287562	synonymous-codon	KMT2A	GRCh38.p7	11:118498441	CACCAGCAACTATCA[C/T]TTCATGTGTTCCCGA	4297
rs782712716	snp	G/T	3.30874e-05	0.00406726	missense	KMT2A	GRCh38.p7	11:118481972	AAGTCAAGCAAGCAG[G/T]TCTCCCAGCCAGCAC	4297
rs782712792	snp	A/C	1.64803e-05	0.00287052	missense	KMT2A	GRCh38.p7	11:118503505	AAAATGAGAGTCAAT[A/C]CAAAAATGCCCTGAA	4297
rs782713492	snp	C/T	2.20621e-05	0.00332123	missense	KMT2A	GRCh38.p7	11:118436802	CGTCTTCGTCATCGT[C/T]CTCAGCCTCTTCAGG	4297
rs782715103	snp	A/T	0.000131785	0.00811635	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118474144	CCTTTCCACTCCTTC[A/T]TCTAGCACTGTTAAA	4297
rs782716433	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118461690	GATGTCTCCTGTACC[C/T]TCTCTCTTCAGGGCT	4297
rs782716600	snp	C/T	3.32591e-05	0.0040778	intron-variant, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519586	CCTGTTGACTGCGCT[C/T]CTCACTTCCCTGGTG	4297
rs782717207	snp	A/C	1.64885e-05	0.00287123	missense	KMT2A	GRCh38.p7	11:118510043	GAAAGCATTACTGAG[A/C]AAAAACCCAAGAAAG	4297
rs782717776	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118458633	AGAAGACAAATGTGT[A/G]AACACATTTTTTAAA	4297
rs782718488	snp	C/T	1.7184e-05	0.00293117	synonymous-codon	KMT2A	GRCh38.p7	11:118490224	TTTCTCACTGTGTCA[C/T]GATTGCGCCAAGCTC	4297
rs782718622	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118464409	GTGTAGTAGTGCATG[C/T]CTGTAGTCCCAGCTA	4297
rs782719601	snp	A/G	1.65575e-05	0.00287724	missense	KMT2A	GRCh38.p7	11:118507542	AGGACTCCAGGAGCA[A/G]AGGCTGAGCAGCAGG	4297
rs782719950	snp	A/T	1.64808e-05	0.00287057	missense, intron-variant	KMT2A	GRCh38.p7	11:118474014	CTGTGACTCTTGGGG[A/T]TACAACAGCTGTCAA	4297
rs782720565	in-del	-/G	3.30628e-05	0.00406575	intron-variant	KMT2A	GRCh38.p7	11:118484143	ATGTGAAGGCAAATA[-/G]GGTGTGATTTTGTTC	4297
rs782721532	snp	A/G	1.64762e-05	0.00287016	missense, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118522117	CCATTGAGGATGCCA[A/G]CAACAAGCTGCCCTG	4297
rs782721568	snp	C/T	1.73525e-05	0.0029455	missense	KMT2A	GRCh38.p7	11:118491917	ACCAGCCATTTGCTA[C/T]GCTACCGGCAGGTAG	4297
rs782721966	snp	C/G	1.70359e-05	0.0029185	intron-variant	KMT2A	GRCh38.p7	11:118509208	AAGTGCAGGTATGTG[C/G]GTGGGTAAAAGGTTA	4297
rs782722258	snp	C/T	1.66927e-05	0.00288895	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473265	GAGAGCTCCAAGATT[C/T]ACTCCAAGTGAGGCT	4297
rs782723403	snp	A/G	1.64779e-05	0.00287031	missense, intron-variant	KMT2A	GRCh38.p7	11:118473960	AAGCAACAGGGCGGA[A/G]GAAGTCTTCATCACA	4297
rs782723723	snp	A/G	1.66117e-05	0.00288194	missense, intron-variant	KMT2A	GRCh38.p7	11:118473698	GGCTCTCAGACTGAA[A/G]GAGGGAGAAATAAAG	4297
rs782723872	snp	A/G			missense	KMT2A	GRCh38.p7	11:118501108	ACTGTTGAACATGAT[A/G]AAAACAGGACCATTG	4297
rs782725093	snp	A/C/T	3.30553e-05	0.00406531	missense	KMT2A	GRCh38.p7	11:118481913	AAGGGAATGTCTCGG[A/C/T]CCCTGGGCCTGAATC	4297
rs782727037	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118457125	TTGGCAGCAAAAATC[C/G]AAATCTAATCATACT	4297
rs782727086	snp	C/T	1.64882e-05	0.00287121	missense	KMT2A	GRCh38.p7	11:118506142	TGGGGACATCACAGA[C/T]CCCCTCTACTGCTGC	4297
rs782727635	snp	A/C	3.29484e-05	0.00405871	missense	KMT2A	GRCh38.p7	11:118499375	ATCAGCTTGAGAAGG[A/C]AGTTTCTCAATGGCT	4297
rs782727718	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118452510	GCACTCCAGCCTGGG[C/T]GACAGAATAAGACCC	4297
rs782728249	snp	A/G	1.654e-05	0.00287571	missense	KMT2A	GRCh38.p7	11:118504132	AGATTCCAAAAAGAA[A/G]TGGTAAAGAAAATGG	4297
rs782728957	snp	A/G	3.36378e-05	0.00410094	synonymous-codon	KMT2A	GRCh38.p7	11:118506599	GACCAGTTCTTCTGA[A/G]GCACACATTCCAGAC	4297
rs782730000	snp	C/T			upstream-variant-2KB	KMT2A	GRCh38.p7	11:118436269	GCGGGCAGGAGGCGG[C/T]GGCCCGGGCCTCGGG	4297
rs782730461	snp	A/G	1.64898e-05	0.00287135	missense	KMT2A	GRCh38.p7	11:118495768	CTCAGTGGCAGGAGC[A/G]AGAGGAAAACAGCCA	4297
rs782730865	snp	A/C/T	1.64735e-05	0.00286993	missense, synonymous-codon	KMT2A	GRCh38.p7	11:118493155	TCTTACTGAGGTCAG[A/C/T]AAACAGGATGATCAG	4297
rs782730962	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118506968	TTGAGGGCAAAGCTC[C/T]CTCTTGTAGATCCAC	4297
rs782731643	snp	A/T	1.65042e-05	0.0028726	intron-variant	KMT2A	GRCh38.p7	11:118498091	AAGACCTTATGGGTA[A/T]ATTTTATGAAAGAGA	4297
rs782731658	snp	C/T	1.64732e-05	0.0028699	synonymous-codon	KMT2A	GRCh38.p7	11:118506335	TTCTGCTTCAGGGCC[C/T]CAGGTATCCAACTTT	4297
rs782732033	snp	A/T	1.70281e-05	0.00291783	missense, intron-variant	KMT2A	GRCh38.p7	11:118472122	GGGTCTCCTCATTAA[A/T]TCTGAACTGGAAAAG	4297
rs782732392	snp	A/G	1.88624e-05	0.00307097	intron-variant	KMT2A	GRCh38.p7	11:118471621	AAACCTAAACTACAC[A/G]GCTAAATATATGCTC	4297
rs782732794	snp	A/G			missense	KMT2A	GRCh38.p7	11:118503633	CCAAGCCCCAATAAT[A/G]CCTCATGCCAGGATT	4297
rs782732945	snp	A/C/T	0.000100072	0.00707299	intron-variant	KMT2A	GRCh38.p7	11:118480135	AGTGCTTTTCTTCTA[A/C/T]ATTTAATTTGTTTCA	4297
rs782733088	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118513428	AATTTTATCAGTGAT[A/G]TTCTTCCTTTAAGAG	4297
rs782733922	snp	A/G	1.64765e-05	0.00287019	missense, intron-variant	KMT2A	GRCh38.p7	11:118472888	CTGCAGCCAGCCTCC[A/G]GTATCTCTGACCACA	4297
rs782734171	snp	G/T	1.64751e-05	0.00287007	missense	KMT2A	GRCh38.p7	11:118501785	CATGTCATCTCAAAG[G/T]TCCCCAGGATTCGAA	4297
rs782734515	snp	C/G	1.64787e-05	0.00287038	missense	KMT2A	GRCh38.p7	11:118503955	ACTATTACAACTTCA[C/G]TAGAACAGTGATTTC	4297
rs782735656	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118483612	TTCTTTGTGGCCCCA[A/C]ATGTTCTAGCCTAGG	4297
rs782735983	in-del	-/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521609	AGTACAGAAAGTTGC[-/T]TCTTAGAAGGTTTGT	4297
rs782736692	snp	A/T	1.65119e-05	0.00287327	intron-variant	KMT2A	GRCh38.p7	11:118477952	CTTGGAACTAATGCC[A/T]CATTTCTTTAACAGA	4297
rs782736916	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118496857	TTAAAATGAAGATAA[G/T]AACGCTTACCTCAGA	4297
rs782736936	snp	A/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521042	TCCTGCACCTCCTTG[A/T]GTTGAACAAGGACTT	4297
rs782737765	snp	C/T	1.6492e-05	0.00287154	missense	KMT2A	GRCh38.p7	11:118504060	CACAGTTGGATGGTG[C/T]TGATGATGGGACAGA	4297
rs782738245	snp	C/T	1.8449e-05	0.00303713	intron-variant	KMT2A	GRCh38.p7	11:118481665	TAATTCTATTTTAAA[C/T]AAAATTATTCTCACT	4297
rs782738899	snp	A/G/T	3.2948e-05	0.00405871	missense	KMT2A	GRCh38.p7	11:118505560	CCTCTGGACTCAAGA[A/G/T]AAGACCCATATCTCG	4297
rs782739191	snp	C/T	1.65315e-05	0.00287498	synonymous-codon	KMT2A	GRCh38.p7	11:118503224	TTTCAAAGAAAAGCA[C/T]TCCAGTAAATCTTTT	4297
rs782739484	snp	A/G	1.65165e-05	0.00287367	missense	KMT2A	GRCh38.p7	11:118481843	GAGGATCCTGCCCCA[A/G]AGAAAAGCAGTAGTG	4297
rs782739856	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118467993	GAACTTGTGCAAAAT[-/A]GGTTAAACAAATCCT	4297
rs782741215	snp	A/G	0.000232504	0.0107795	synonymous-codon	KMT2A	GRCh38.p7	11:118436704	TGTGGCGGCCGCGGC[A/G]GCGGCGGCGGGAAGC	4297
rs782741633	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118499736	AGTGAGCTGAGATTG[C/T]GCCACTGCATTCCAG	4297
rs782743581	snp	A/C	1.64762e-05	0.00287016	missense	KMT2A	GRCh38.p7	11:118502545	TGTCTCCAATGAGAA[A/C]TGGGAATACTTACTC	4297
rs782744154	in-del	-/GCG/GCGGCGGCG	0	0	cds-indel	KMT2A	GRCh38.p7	11:118436698	CCGGCTGTGGCGGCC[-/GCG/GCGGCGGCG]GCGGCGGCGGCGGCG	4297
rs782744821	snp	A/C	1.66932e-05	0.002889	synonymous-codon	KMT2A	GRCh38.p7	11:118494762	GCCAAATAAAGTATC[A/C]AGCAAGTAAGTGAAT	4297
rs782744910	snp	A/T	1.67489e-05	0.00289381	intron-variant	KMT2A	GRCh38.p7	11:118507612	GGCAACCTGCAGGGT[A/T]AGCTGAAGAATTCGT	4297
rs782744952	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118442939	ACCTGGACCCAGATG[C/G]CTTCATTGATCACAT	4297
rs782745599	snp	A/G	3.29679e-05	0.00405991	missense	KMT2A	GRCh38.p7	11:118505238	GTTAGTTCTACACCC[A/G]GTGTGATGGAGACAA	4297
rs782746928	snp	G/T	1.64972e-05	0.00287199	missense, intron-variant	KMT2A	GRCh38.p7	11:118473486	CCCCCCCGTCTTCTG[G/T]CTCTTCCTCGTTAAG	4297
rs782748241	snp	G/T	1.65263e-05	0.00287452	intron-variant	KMT2A	GRCh38.p7	11:118484145	GTGAAGGCAAATAGG[G/T]TGTGATTTTGTTCTA	4297
rs782748892	snp	C/G	1.64819e-05	0.00287066	missense	KMT2A	GRCh38.p7	11:118506009	ACCAACCCAAGGTTG[C/G]TTGGTACCCCAGATA	4297
rs782750298	snp	A/G	1.65304e-05	0.00287488	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521468	TTTTGCTGTAGAAAG[A/G]GACCAGTATGACCCC	4297
rs782751175	snp	G/T	1.65184e-05	0.00287384	intron-variant	KMT2A	GRCh38.p7	11:118491183	ACTGCTGTAAACTTT[G/T]CTTTGCTTTCAGGAA	4297
rs782751440	snp	A/G/T	8.43926e-05	0.00649542	intron-variant	KMT2A	GRCh38.p7	11:118488504	TATGTATTGAATTAA[A/G/T]TATATGCCAGTGGAC	4297
rs782751697	snp	A/T	3.40768e-05	0.00412762	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520927	ACAGAAAACGAATGC[A/T]GTTTTTCAAAATCAA	4297
rs782752523	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118438513	GCGAAGGGGGGTAGG[A/G]GGTTGCTGCTCTGGA	4297
rs782753112	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118441150	ATTTCAAAAGTCAGA[A/G]TCAAGTGAGACGATT	4297
rs782753854	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118516912	CATTATCAACACAAT[A/G]TTAATCTCATTGTAA	4297
rs782753944	snp	A/T			intron-variant	KMT2A	GRCh38.p7	11:118468264	CAGAAATCACATCTA[A/T]ATGTCAATTCCTGAG	4297
rs782754391	snp	A/G	3.32591e-05	0.0040778	missense, intron-variant	KMT2A	GRCh38.p7	11:118471925	GATAGCCTGAAAAAA[A/G]TTAAAAGGACACCTT	4297
rs782754583	snp	C/T	3.42607e-05	0.00413874	intron-variant	KMT2A	GRCh38.p7	11:118507638	TTCGTCTTTTAAGAC[C/T]AAGCTCTCAGTTTTG	4297
rs782755319	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118471003	AAGAACCTCTAAGCA[A/G]GGGAGTAGATTTAGT	4297
rs782755322	snp	G/T	1.6477e-05	0.00287024	missense	KMT2A	GRCh38.p7	11:118476839	CAGAGACCTCTGTGC[G/T]AGGACCCCGGATTAA	4297
rs782755833	snp	C/G	1.69752e-05	0.0029133	intron-variant	KMT2A	GRCh38.p7	11:118507511	TGTCTTGAAAAGATA[C/G]AAATGCCTGTGTTCC	4297
rs782757827	snp	A/G	0.000264577	0.0114986	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118472356	GCAGGGAAGAAAGGT[A/G]AAGACACAGGTCAAA	4297
rs782758095	snp	C/T	1.67223e-05	0.00289151	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520755	ATTCAAGACTCAAAA[C/T]ATTATTTCCTGAAAA	4297
rs782758288	snp	A/G	1.64866e-05	0.00287106	missense	KMT2A	GRCh38.p7	11:118504315	AGCTCAGCTCATTGG[A/G]GTCAAGCCGCAGAGT	4297
rs782758324	snp	C/G	1.64735e-05	0.00286993	missense	KMT2A	GRCh38.p7	11:118491807	CTTGTGTGAACTGTA[C/G]TGAGCGGCACCCTGC	4297
rs782759164	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118490017	CTCATTACTAGGAAA[C/T]CATCTCAGCAGAGAA	4297
rs782759721	snp	A/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118512125	AAAAATCAGTTAAAA[A/T]TTTTTTTCACAGCTT	4297
rs782760872	snp	C/G	9.89576e-05	0.00703342	synonymous-codon	KMT2A	GRCh38.p7	11:118501029	AGATGCTCGCAAGCG[C/G]TGTGTATATACATGC	4297
rs782760907	snp	C/G	1.66037e-05	0.00288125	intron-variant	KMT2A	GRCh38.p7	11:118468731	GGATGTGTTTGTATG[C/G]ACGTTTTTGCTTCTG	4297
rs782761669	snp	C/G/T	9.89159e-05	0.00703201	missense	KMT2A	GRCh38.p7	11:118506025	TTGGTACCCCAGATA[C/G/T]TGGCTCAATAAGCAA	4297
rs782761989	snp	A/C	1.64925e-05	0.00287158	missense	KMT2A	GRCh38.p7	11:118495779	GAGCGAGAGGAAAAC[A/C]GCCACACTGAGCAGC	4297
rs782761996	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118466362	AAGACTCACTATGTT[A/G]CCCAGGCTAGCCTTG	4297
rs782762976	snp	C/T	1.64754e-05	0.00287009	synonymous-codon	KMT2A	GRCh38.p7	11:118502963	CTCCTTTGCTGAACC[C/T]TCTTCAGTGTCGTTT	4297
rs782763882	snp	C/T	9.3194e-05	0.00682556	intron-variant	KMT2A	GRCh38.p7	11:118471636	AGCTAAATATATGCT[C/T]TTCATTGTTTAATTT	4297
rs782763989	snp	A/G	3.32574e-05	0.00407769	missense	KMT2A	GRCh38.p7	11:118506583	AAGTTTCCCATTTGC[A/G]GACCAGTTCTTCTGA	4297
rs782764234	snp	A/C	1.64727e-05	0.00286986	missense	KMT2A	GRCh38.p7	11:118505908	TGTCTGGCTTGGCAT[A/C]CAGTTCCTCTGTCTT	4297
rs782764703	snp	A/G			utr-variant-3-prime, intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118523411	GCTAAAGTAAATTCA[A/G]TGACACTACTGCCCT	4297
rs782765039	snp	A/G	1.64781e-05	0.00287033	missense	KMT2A	GRCh38.p7	11:118504561	GTCTTGACAGTAATC[A/G]TGAAAAAGACATGGG	4297
rs782765477	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118464152	TCATCTTGTTCATGC[C/T]GTAATTGAAGAGGAA	4297
rs782766701	snp	A/C			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118514269	ACAGTCGCTGAGTAG[A/C]GACCCAGCCCTGCTC	4297
rs782768278	snp	A/G	3.29864e-05	0.00406105	missense	KMT2A	GRCh38.p7	11:118501028	CAGATGCTCGCAAGC[A/G]CTGTGTATATACATG	4297
rs782768622	snp	A/C			intron-variant	KMT2A	GRCh38.p7	11:118507325	ATACAGAACATTTCT[A/C]GCAACCCACAAGGGT	4297
rs782768624	snp	A/C	2.29329e-05	0.00338614	synonymous-codon	KMT2A	GRCh38.p7	11:118436815	GTCCTCAGCCTCTTC[A/C]GGGCCGGCCCTGCTC	4297
rs782768829	snp	C/T	1.64982e-05	0.00287208	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473073	CTCAGCAAAGTATGC[C/T]AAAGAAGGTCTTATT	4297
rs782769037	snp	C/T	6.65845e-05	0.00576956	intron-variant	KMT2A	GRCh38.p7	11:118438995	AGATTATTATTTTTT[C/T]TTGAAAGGCCAATTC	4297
rs782770260	snp	G/T	1.7345e-05	0.00294486	intron-variant	KMT2A	GRCh38.p7	11:118495936	CCATTTCCCTCTAGA[G/T]GCAGATGATTGACTT	4297
rs782771192	in-del	-/G			intron-variant	KMT2A	GRCh38.p7	11:118439169	CAGCAAAAAAAAAAA[-/G]AAAAGAAAAAAAAGA	4297
rs782771544	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118460315	TTTTTCTGAGATAGG[C/G]ACTTGCTCTGTCACC	4297
rs782771940	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118453368	GTTAAACCCTTTGGC[-/A]GCCTTTGAACCAGCT	4297
rs782771955	snp	C/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519843	CTCGATTTTCTTATC[C/T]CATGACACTGTCATC	4297
rs782772276	snp	C/T	1.71531e-05	0.00292852	intron-variant	KMT2A	GRCh38.p7	11:118501627	TAATTTGTTTGATAT[C/T]TTAATTGGGCCTTTT	4297
rs782772360	snp	A/G	4.94214e-05	0.00497074	synonymous-codon	KMT2A	GRCh38.p7	11:118505762	CCCCAACATCATAAA[A/G]AGATCTAAATCTAGC	4297
rs782773165	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118510537	AGATCCAGCTCAGAC[G/T]GTCTTCCCTGACCTT	4297
rs782775238	snp	G/T	1.65405e-05	0.00287576	intron-variant	KMT2A	GRCh38.p7	11:118484321	GACTTTAAGGTAAAG[G/T]TGTTCAGTGATCATA	4297
rs782775875	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118456813	CCTTTAGACAACGTG[G/T]ATAAACATTTCAAAT	4297
rs782775993	snp	C/T	2.20218e-05	0.0033182	missense	KMT2A	GRCh38.p7	11:118436793	CCTCGTCTTCGTCTT[C/T]GTCATCGTCCTCAGC	4297
rs782776155	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118515205	TCATATCAGCATAAC[A/G]TGGTTGATGCAGTTC	4297
rs782776461	snp	C/T			synonymous-codon	KMT2A	GRCh38.p7	11:118503527	TGCCCTGAAAGAAAG[C/T]AGTCCTGCTTCCCCT	4297
rs782778561	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521179	TTTATTTTCTCAAGT[A/G]TATGTCCCTCCTGGG	4297
rs782778643	snp	C/G	1.65102e-05	0.00287312	missense	KMT2A	GRCh38.p7	11:118484865	CTCTCTCCACAGGAG[C/G]ATTGTGAAGCAGAAA	4297
rs782779403	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118475234	GTTAAGATGATGCCA[A/G]ATATTTTTACAAAGA	4297
rs782779444	in-del	-/T	1.68701e-05	0.00290427	intron-variant	KMT2A	GRCh38.p7	11:118484989	GGTAAGGCATCCTGC[-/T]TTCTTTGTACCCCAG	4297
rs782779521	snp	A/G	3.64352e-05	0.00426805	missense	KMT2A	GRCh38.p7	11:118491924	ATTTGCTACGCTACC[A/G]GCAGGTAGGCCAAGT	4297
rs782781212	snp	A/G	6.60338e-05	0.00574566	missense, intron-variant	KMT2A	GRCh38.p7	11:118472730	CAGAAAATGAGAGTA[A/G]TGATAGGAGAAGCAG	4297
rs782782024	snp	A/G	4.95864e-05	0.00497903	missense	KMT2A	GRCh38.p7	11:118481939	GAATCCAAACAGGCC[A/G]CCACTCCAGCTTCCA	4297
rs782782746	snp	A/C	0.000198409	0.00995818	intron-variant	KMT2A	GRCh38.p7	11:118468747	ACGTTTTTGCTTCTG[A/C]TTTTAAAATAATTTT	4297
rs782782893	snp	A/G	1.64822e-05	0.00287068	missense	KMT2A	GRCh38.p7	11:118484258	CTCTCCAATGGCAAT[A/G]GTTCTAAGCAAAAAA	4297
rs782784187	snp	A/G	1.64819e-05	0.00287066	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473985	ATCACATGATTCTGG[A/G]ACTGATATTACTTCT	4297
rs782784333	snp	C/T	6.6096e-05	0.00574836	missense	KMT2A	GRCh38.p7	11:118504165	CAGAGAACTTAAAGA[C/T]TGATAGACCTGAAGA	4297
rs782784769	snp	A/G	3.31076e-05	0.0040685	intron-variant	KMT2A	GRCh38.p7	11:118480153	TTAATTTGTTTCATG[A/G]TTTATTCGTTGTTTT	4297
rs782784936	snp	C/T			upstream-variant-2KB	KMT2A	GRCh38.p7	11:118435849	TTTCTGTTTTGCATA[C/T]AGTAAACTGGGCAGC	4297
rs782785261	snp	A/G	4.95299e-05	0.00497619	synonymous-codon	KMT2A	GRCh38.p7	11:118481791	TGTTGTGAAGAACGT[A/G]GTGGACTCTAGTCAG	4297
rs782785673	snp	A/G	1.6612e-05	0.00288196	missense	KMT2A	GRCh38.p7	11:118498503	AAGTATATTGCCAAC[A/G]ACATCGGGATTTGAT	4297
rs782785709	snp	A/G	6.59022e-05	0.00573993	missense	KMT2A	GRCh38.p7	11:118506250	AAGCAGACGAACACT[A/G]TCAGCTTCAGCATGT	4297
rs782786105	snp	G/T	1.64844e-05	0.00287087	missense	KMT2A	GRCh38.p7	11:118477972	TCTTTAACAGACAAG[G/T]CATCAATTGCTGGCT	4297
rs782786807	snp	C/T	0.000260981	0.0114203	intron-variant	KMT2A	GRCh38.p7	11:118488523	ATGCCAGTGGACTAC[C/T]AAAACCCAAAGTATA	4297
rs782788461	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118488112	TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGT	4297
rs782788552	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118457375	TGGGTTCAAGCGATT[C/G]TCCGCCTCAGCCTCC	4297
rs782788997	snp	A/G	1.64776e-05	0.00287028	missense	KMT2A	GRCh38.p7	11:118505994	GGACACGTCACCTTA[A/G]CCAACCCAAGGTTGC	4297
rs782789544	snp	A/G	1.64762e-05	0.00287016	missense, intron-variant	KMT2A	GRCh38.p7	11:118474166	ACTGTTAAACATTCC[A/G]CTTCCTCCATAGGCT	4297
rs782789725	snp	C/T	6.59055e-05	0.00574007	missense	KMT2A	GRCh38.p7	11:118502523	CAGCGGTCCAAACTC[C/T]GGATAATGTCTCCAA	4297
rs782789739	snp	C/T	1.64923e-05	0.00287156	missense	KMT2A	GRCh38.p7	11:118505275	CAGTATTGGGACCCA[C/T]GGGAGGTGGTCTCAC	4297
rs782789983	snp	C/T	1.65217e-05	0.00287412	missense, intron-variant	KMT2A	GRCh38.p7	11:118472693	CCTGAAGTTCATCCT[C/T]CACTGCCCATTTCCC	4297
rs782791496	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118446071	AAAGATTTGCAGGCC[A/G]GGTGGGGTGGCTCAA	4297
rs782791692	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118480897	GTCTTGAACTCCTGG[A/G]CTCAAGCAATCCTCT	4297
rs782793053	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118476523	TTGTGTAGAGATGGG[C/T]TCTCGCTATGTTGCC	4297
rs782793308	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118515838	GGACTACAGGTACAC[A/G]CCACCACACCCAGCT	4297
rs782794087	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118442768	CTTCTAGAGTATTTT[C/T]AGAATAAGATAAAAT	4297
rs782794345	snp	A/T	0.000209358	0.0102291	upstream-variant-2KB	KMT2A	GRCh38.p7	11:118435096	GTGCGGGAGTCCAGG[A/T]AGGCTGCATGACCTT	4297
rs782794908	in-del	-/T	1.65026e-05	0.00287246	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118521448	GCACTCACACAGTTC[-/T]TTTGTTTTGCTGTAG	4297
rs782795153	snp	A/T	1.69677e-05	0.00291266	missense, intron-variant	KMT2A	GRCh38.p7	11:118472084	GGAAGGCCTCCATCA[A/T]CAGAAAGGATAAAGA	4297
rs782795995	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118508388	CTACAATATTTTAAT[A/G]AGTCCTCTATTGATA	4297
rs782797135	snp	A/G	3.29571e-05	0.00405924	missense	KMT2A	GRCh38.p7	11:118503301	CAGAGTTTATGGATG[A/G]GGTTTTGACTCCTGA	4297
rs782797240	snp	A/G	4.94996e-05	0.00497467	synonymous-codon	KMT2A	GRCh38.p7	11:118505360	TGCTAGCAAAGGATT[A/G]CTACCCATGTCTCAT	4297
rs782797798	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118444540	ACTGCCTGAGTTCAA[A/G]TCTAAGCTCAGCCAT	4297
rs782797999	snp	A/G	3.29946e-05	0.00406155	missense	KMT2A	GRCh38.p7	11:118502659	GGCCACTGAATTCAA[A/G]TACTAGTTTAGGGCA	4297
rs782798879	snp	A/G	1.65119e-05	0.00287327	missense, intron-variant	KMT2A	GRCh38.p7	11:118473098	CTTATTCGCAAACCA[A/G]TATTTGATAATTTCC	4297
rs782799010	snp	A/G	1.77944e-05	0.00298276	intron-variant	KMT2A	GRCh38.p7	11:118509240	AATCAGAGAATATCA[A/G]TGCTAAAAGGATTAT	4297
rs782799073	snp	C/G	1.64741e-05	0.00286998	missense	KMT2A	GRCh38.p7	11:118493118	CTTCCCGCAGCTCCC[C/G]CGAAGGACCTGATCC	4297
rs782799412	snp	C/T	1.68707e-05	0.00290432	missense	KMT2A	GRCh38.p7	11:118491908	TCTCGGACTACCAGC[C/T]ATTTGCTACGCTACC	4297
rs782799419	snp	A/C	1.75761e-05	0.00296441	intron-variant	KMT2A	GRCh38.p7	11:118439007	TTTTTTGAAAGGCCA[A/C]TTCTGTATTTTTTAA	4297
rs782800112	snp	C/T	0.000148254	0.00860844	missense	KMT2A	GRCh38.p7	11:118505068	CTGATAGTCCTGGCC[C/T]GTCTCAGATTTCCAA	4297
rs782800336	snp	A/C	1.64773e-05	0.00287026	synonymous-codon	KMT2A	GRCh38.p7	11:118503995	AGAGGAACGACTGGC[A/C]TCCCATAATTTATTT	4297
rs782800923	snp	A/G	1.67189e-05	0.00289122	missense	KMT2A	GRCh38.p7	11:118474302	TTAAACAAACCGACC[A/G]GCCCAAAGCACAGGT	4297
rs782802145	snp	C/T			upstream-variant-2KB, utr-variant-3-prime, intron-variant	TTC36, KMT2A, LOC101929089	GRCh38.p7	11:118525761	CTTCTAAGTTCGGTT[C/T]GGGATTTTTTTTTTT	4297
rs782802602	snp	A/G	1.65688e-05	0.00287821	missense, intron-variant	KMT2A	GRCh38.p7	11:118471874	AAAATAACACATGGA[A/G]AGGACATTTCAGAGT	4297
rs782803269	snp	C/T	1.88677e-05	0.0030714	intron-variant	KMT2A	GRCh38.p7	11:118482117	GAGGGCAAGAAGGAA[C/T]TGCTGAACCACAAGT	4297
rs782804513	snp	C/T	1.64928e-05	0.00287161	synonymous-codon	KMT2A	GRCh38.p7	11:118499848	AGGGTCTATGACAAT[C/T]GACTGCTTAGGAATT	4297
rs782806241	in-del	-/A			intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118519303	CTGCCCTGTGTGGTC[-/A]TTATGAGCACGAAAT	4297
rs782806555	snp	C/T	5.67832e-05	0.00532808	intron-variant	KMT2A	GRCh38.p7	11:118494658	GTATCTAAATGAGTG[C/T]TTACATATTTACATT	4297
rs782807569	snp	A/C	1.67047e-05	0.00288999	intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118520902	TATGACTAAAATTCT[A/C]GAAAGAATTACAGAA	4297
rs782808474	snp	C/T	3.37234e-05	0.00410616	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118471705	GAGACCTAGAAGTGG[C/T]TCTGACCGAAATTCA	4297
rs782808603	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118443341	TTTAAAATGATGAGC[C/T]GCTTTTCTTGACCTA	4297
rs782809939	snp	A/G	3.295e-05	0.00405881	synonymous-codon	KMT2A	GRCh38.p7	11:118503617	TGGTCCAGTGGCCCA[A/G]CCAAGCCCCAATAAT	4297
rs782810170	snp	C/T			intron-variant	KMT2A	GRCh38.p7	11:118467943	ATCATTGAATTTCTA[C/T]TAATCAGTTTGTTTA	4297
rs782811050	snp	A/G	8.24232e-05	0.0064191	missense	KMT2A	GRCh38.p7	11:118506022	TGCTTGGTACCCCAG[A/G]TATTGGCTCAATAAG	4297
rs782811073	snp	A/G			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118518139	ACTGTTTCTATATCT[A/G]TTAATAATACCAAAC	4297
rs782811887	snp	A/G	1.70197e-05	0.00291711	intron-variant	KMT2A	GRCh38.p7	11:118495908	AGTAAGCCACCAAAA[A/G]GAGAGTCGTCACCCA	4297
rs782812412	snp	A/T	1.65132e-05	0.00287339	intron-variant, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118519613	GGTGCTTCTGATTCT[A/T]CTAGGTGTTAACGGT	4297
rs782812514	in-del	-/A			intron-variant	KMT2A	GRCh38.p7	11:118469507	GTCATTATTCTCACC[-/A]AACAAAATATCTAGA	4297
rs782813188	snp	A/G	1.66441e-05	0.00288474	missense	KMT2A	GRCh38.p7	11:118490180	TCCACAACTCCAGGC[A/G]AAGGGTGGGATGCAC	4297
rs782813354	snp	G/T			intron-variant	KMT2A	GRCh38.p7	11:118464810	GCAGACTGTTTAAGA[G/T]CAAAGGTCATGGCAA	4297
rs782814987	snp	C/G	1.65875e-05	0.00287984	synonymous-codon, intron-variant	KMT2A	GRCh38.p7	11:118473685	TTGGTTTACCCCAGG[C/G]TCTCAGACTGAAAGA	4297
rs782815641	snp	C/T	1.64768e-05	0.00287021	missense, intron-variant	KMT2A	GRCh38.p7	11:118472870	CTGACTCCACCGCCA[C/T]CACTGCAGCCAGCCT	4297
rs782816031	snp	A/G	0.000119012	0.0077131	intron-variant, nc-transcript-variant	KMT2A, LOC101929089	GRCh38.p7	11:118511928	TATTTTCTGGCTTAC[A/G]GGTTTTCTTTATTTC	4297
rs782816466	snp	A/G	6.59011e-05	0.00573988	missense	KMT2A	GRCh38.p7	11:118506501	TCAGTGCCGGGTCCC[A/G]CTAAACCCAAACCAA	4297
rs782817600	snp	C/T	1.64779e-05	0.00287031	synonymous-codon	KMT2A	GRCh38.p7	11:118496367	TGATGACAGTGCTAA[C/T]GTAAGTACTTTGCAA	4297
rs782817695	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118500104	CGGAATCCAGTTATA[A/G]AAGGAAAGTATTATT	4297
rs782818085	snp	C/T	1.70647e-05	0.00292097	intron-variant	KMT2A	GRCh38.p7	11:118507632	GAAGAATTCGTCTTT[C/T]AAGACTAAGCTCTCA	4297
rs782818534	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118459925	GTCTCAAACTCCTGA[C/G]CTCAAGTGATCTGCC	4297
rs782818853	snp	A/G	0.000164728	0.00907398	missense, intron-variant	KMT2A	GRCh38.p7	11:118473861	GATCAGAAATTCAGA[A/G]TAGTTCTGCTTTGTA	4297
rs782818980	snp	A/G			intron-variant, downstream-variant-500B	KMT2A, LOC101929089	GRCh38.p7	11:118511773	GGAGTGTACCTTTTC[A/G]GCTCCTTTCACATGT	4297
rs782818984	snp	A/G			intron-variant	KMT2A	GRCh38.p7	11:118462250	TGAACCACCATGCCC[A/G]GCTGCAGCACCCTCT	4297
rs782819380	in-del	-/TCGTCGTCCGCCTCGTCT	2.36902e-05	0.00344159	cds-indel	KMT2A	GRCh38.p7	11:118436767	GCCTCAGCAGCCTCC[-/TCGTCGTCCGCCTCGTCT]TCGTCGTCCGCCTCG	4297
rs782820569	snp	C/G			intron-variant	KMT2A	GRCh38.p7	11:118501267	GTTCAAGAACAGCCT[C/G]GCCAACATGGTGAAA	4297
rs782821114	snp	C/T			intron-variant	KMT2A, LOC101929089	GRCh38.p7	11:118513709	AACATCTTGGGAGGA[C/T]TGTTTGAGTCTAGGA	4297
rs796281679	in-del	-/T			intron-variant	KMT2A	GRCh38.p7	11:118451673	TTTTTTTTTTTTTTT[-/T]GTAGAGATGGGGTCT	4297
rs797044565	in-del	-/CAGT			frameshift-variant	KMT2A	GRCh38.p7	11:118503457	CACCACGGAAACGCA[-/CAGT]CAAAGTGACACTGAC	4297
rs797044937	in-del	-/A			frameshift-variant, intron-variant	KMT2A	GRCh38.p7	11:118473027	GGTGGACTTCTTTAA[-/A]GCATTCTAGGTCAGA	4297
rs797045051	snp	A/C			missense	KMT2A	GRCh38.p7	11:118495830	ATTCCAGCTCCCAAA[A/C]CCAAAGGTCCTGGAG	4297
rs797045656	in-del	-/A			frameshift-variant	KMT2A	GRCh38.p7	11:118502703	TCTTCAAATTTGCAA[-/A]GGACAGTGGTTACTG	4297
rs863224887	in-del	-/G			frameshift-variant	KMT2A	GRCh38.p7	11:118481731	GTGAAAAAGAAAGAG[-/G]AAAAAGTCTAAGACC	4297
rs863224888	in-del	-/C			frameshift-variant	KMT2A	GRCh38.p7	11:118506226	AACAGCCGCTTCACC[-/C]TTCTGGGGAAGCAGA	4297
rs863224889	snp	A/G			splice-donor-variant	KMT2A	GRCh38.p7	11:118482496	AAACCAAAAGAAAAG[A/G]TGAGGAGAGATTTGT	4297
rs863224895	snp	C/T			missense	KMT2A	GRCh38.p7	11:118488623	CTATAGTTTGTGTAT[C/T]GCCAAGTCTGTTGTG	4297
rs864309568	snp	C/G			missense, intron-variant	KMT2A	GRCh38.p7	11:118474064	AAAGGGAGAGGAAAT[C/G]TGGAAAAAACCAACT	4297
rs864309569	snp	C/G			stop-gained	KMT2A	GRCh38.p7	11:118501681	CCACAGAAAGTTCAT[C/G]AAAAGAGAGTCAAAA	4297
rs522707	snp	A/G	0	0				:	TAACGCTATGCTCGA[A/G]GCGCCCTCCCCTCTT	4297
rs658411	snp	A/C	0	0				:	TAACTTAATGTAATA[A/C]AAACCAGTTATTTTG	4297
rs693023	snp	C/T	0	0				:	TCCAGTATAACGCGG[C/T]GGCTGGGTCGGGGAG	4297
rs1939735	snp	A/G	0.00394476	0.0442359				:	CCCTGGGCTGACATA[A/G]AATTCTAAAGACTGC	4297
rs2205076	snp	A/G	0	0				:	GTGTCTCTGTCCTTA[A/G]CAGAGCCTTGGGGCT	4297
rs9332861	snp	A/C	0.00331674	0.0405878				:	ACATGTCAAATGCTG[A/C]CTTCCTGGGGCCAAA	4297
rs199657206	snp	C/T						:	ACTTGCTATCTAATT[C/T]TTTTTTTTTTTTTTT	4297
rs200278958	snp	A/G						:	CTAAAGTTTAATTTT[A/G]TTTTTTTTTTTTTTT	4297
rs548774171	snp	A/G	0.000399281	0.0141238				:	CAGTAGAGCGAGGAG[A/G]TGGCAGGAGACCTGC	4297

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