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

MYCBP2

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs74679458	snp	A/G	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77208392	CTTCCACATGTGTGT[A/G]AAACTCTGTGTGTAG	23077
rs74700316	snp	C/T	0.0614824	0.164198	intron-variant	MYCBP2	GRCh38.p7	13:77207798	TTTAAGATTTCCCCT[C/T]GGTCTTTAGTGTTCA	23077
rs74707095	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77277774	ACATGCTAATGAGAA[C/T]TGAGAACCACATAAT	23077
rs74744261	snp	A/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77314744	CAAGAGTGAACCCTA[A/T]TGTAAACTCTGGACT	23077
rs74759343	snp	G/T	0.0614824	0.164198	intron-variant	MYCBP2	GRCh38.p7	13:77146457	AAAACAGATAACATC[G/T]TTTGAGTACATTAAA	23077
rs74794675	snp	C/T	0.0185938	0.0946107	intron-variant	MYCBP2	GRCh38.p7	13:77115205	GACACTGTCAGAAGG[C/T]ACAGGACATAAAATG	23077
rs74799193	snp	C/T	0.0333695	0.124785	intron-variant	MYCBP2	GRCh38.p7	13:77264662	TTCATCAATACTGCA[C/T]GTATCTCCATAGAAT	23077
rs74803093	snp	A/G	0.0146672	0.084371	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291102	TTCCCCCAAAAGCAA[A/G]CCACAGAACAGGAGA	23077
rs74807428	snp	C/T	0.0667028	0.170006	intron-variant	MYCBP2	GRCh38.p7	13:77107867	TGCATAATCAATACA[C/T]CTAATATTCTTCTTT	23077
rs74826208	snp	A/G	0.00953873	0.0683987	intron-variant	MYCBP2	GRCh38.p7	13:77316546	TTTCGCCTATTATAC[A/G]ATTAGGATTCACTTG	23077
rs74859810	snp	A/G	0.0158469	0.0875917	intron-variant	MYCBP2	GRCh38.p7	13:77088766	TAAAAAAGTGGCATC[A/G]TGAAATAGAATCATC	23077
rs74862883	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77104464	GTATACATCACATCA[A/G]GTGCTGAGAAACTTG	23077
rs74863929	snp	A/T	0.0425829	0.139564	intron-variant	MYCBP2	GRCh38.p7	13:77068953	TCAATTTAATACTAT[A/T]CTCCCAGTTAATTCT	23077
rs74875083	snp	C/T	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77217313	ACTACACAAAATTCT[C/T]AGAGCATTTTCACTC	23077
rs74922977	snp	A/G	0.00557542	0.0525036	intron-variant	MYCBP2	GRCh38.p7	13:77238427	ACGAAACAGAGTGCT[A/G]AAAAGGAATATAAGG	23077
rs74933311	snp	C/T	0.000263757	0.0114808	missense	MYCBP2	GRCh38.p7	13:77261297	TTGGAGATTTTGTAA[C/T]TGGTAGCTCAACCCA	23077
rs74966554	snp	C/T	0.124491	0.216211	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77074808	TCCAGGAAAAGGCAA[C/T]ACAACACTGGCAGAA	23077
rs74967649	snp	C/T	0.000381841	0.0138121	missense	MYCBP2	GRCh38.p7	13:77098978	TTCCTGATGTAGAGG[C/T]TGGTTTAGAAGATGT	23077
rs74971347	snp	A/C	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77072595	AGGAAAATCAATGAA[A/C]CAAAAAGCTAGTTCT	23077
rs74985186	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77210147	AAGCTAGAAACACTA[A/G]GAAGGGTAACTTATT	23077
rs75040389	snp	A/C	0.0263992	0.111815	intron-variant	MYCBP2	GRCh38.p7	13:77130676	AGGGGAAAAATGTCT[A/C]TACTGGTTCATCCAC	23077
rs75041072	snp	C/G	0.5	0	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77073756	ATGAACAATTGGAAA[C/G]TGAAATAAAAAATAC	23077
rs75058393	snp	A/C	0.5	0	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228507	GTGAGACCCTGTCTC[A/C]AAAAAAAAAAAAAAA	23077
rs75094931	snp	C/G	0.0607341	0.163335	intron-variant	MYCBP2	GRCh38.p7	13:77316729	CTAGATTCCTTTAAT[C/G]TATGGCTAGTATTTC	23077
rs75095574	snp	G/T	0.0614824	0.164198	intron-variant	MYCBP2	GRCh38.p7	13:77310567	CATATAAATATGTCA[G/T]ATATATGATTATAGA	23077
rs75145274	snp	G/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77164783	ACTTTGGCCCACTTT[G/T]TCCTTGGTTTTATCT	23077
rs75148636	snp	A/G	0.0271762	0.113356	intron-variant	MYCBP2	GRCh38.p7	13:77068150	TTCAAAATCTTTAAG[A/G]AAAGAAATATGATTT	23077
rs75199997	snp	C/T	0.0221141	0.102801	intron-variant	MYCBP2	GRCh38.p7	13:77323356	GAGTAATTAATTCAT[C/T]TGACATTGACTGATA	23077
rs75224607	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77207838	CTAACTCTCTTGATG[G/T]TAAATAATAGAAACA	23077
rs75259844	snp	C/G/T	0.0162398	0.0886349	intron-variant	MYCBP2	GRCh38.p7	13:77300253	TTCCTGAGCCTGTGA[C/G/T]GTAAAGCAGGAATAG	23077
rs75266338	snp	A/G	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77198039	ATCTCTTAGAGCTAG[A/G]AAAAAAAATATCCTC	23077
rs75280078	snp	C/T	0.0225045	0.103662	intron-variant	MYCBP2	GRCh38.p7	13:77284340	AGAAAAGGAGCAAAC[C/T]AGGATAATAGCAGCA	23077
rs75302039	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77137142	TCCTCTAACCTTTGT[A/T]ACTCCCTTCTTTCCC	23077
rs75305491	snp	G/T	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77157104	TAGTTAATTTTTTTT[G/T]GAGATAGGGTCTTGC	23077
rs75318030	snp	C/T	0.00676609	0.0577691	intron-variant	MYCBP2	GRCh38.p7	13:77097271	TAAGATACTATAAAT[C/T]CCCTATCCTTTGACA	23077
rs75325744	snp	A/T	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77307657	AAAAAAAAAAAAACT[A/T]CATTGTATTGAAGTT	23077
rs75338878	snp	C/T	0.0103295	0.0711199	intron-variant	MYCBP2	GRCh38.p7	13:77236290	AGGGGTATGAGATAA[C/T]CAGGTTTAGATAGAA	23077
rs75339559	snp	C/G	0.0614824	0.164198	intron-variant	MYCBP2	GRCh38.p7	13:77222635	TCAAGGACCACTCCC[C/G]ACCCCTGTCCCACCC	23077
rs75341918	snp	A/G	0.0614824	0.164198	intron-variant	MYCBP2	GRCh38.p7	13:77222334	GATATTAGTCATTAA[A/G]TATTTATGATTGTGA	23077
rs75342485	snp	A/T	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77114787	AATAAAAAAAGTATT[A/T]AAAAGTTTCTGGGAG	23077
rs75345734	snp	C/G/T	0.0189856	0.0955633	intron-variant	MYCBP2	GRCh38.p7	13:77297236	GAAAAAAATATGTGA[C/G/T]AAAGAATAAGAATTA	23077
rs75382987	snp	C/T	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77279526	AAACAAAAGACAAAT[C/T]CCATTTCTCAGGCAA	23077
rs75398204	snp	C/T	0.030278	0.119257	intron-variant	MYCBP2	GRCh38.p7	13:77180509	AATTATCTGTCTCTG[C/T]GTATCAAAGTACCAT	23077
rs75403892	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77208759	ATACAGAGTATGACC[A/T]TCCTTTTTCCTGTAT	23077
rs75451147	snp	C/G	0.0325976	0.123435	intron-variant	MYCBP2	GRCh38.p7	13:77153769	TTTTTTTTTAATTCA[C/G]AGGAAGTTTCAAAAA	23077
rs75508205	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77316280	TCATATCAAACAACT[A/G]AAAAATAGGAAAAAC	23077
rs75543926	snp	A/C	0.0356815	0.128715	intron-variant	MYCBP2	GRCh38.p7	13:77094111	TTTTTGTTGCTTATT[A/C]ATTTTATTGTAATAG	23077
rs75563150	snp	A/T	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77307476	ATTAAAAAAAAAAAA[A/T]TTAGCCAGGCACGGT	23077
rs75612389	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77222174	TCTGCATTTCAGTAA[C/T]GTTACTCAATTGCAA	23077
rs75627634	snp	A/T	0.0509478	0.151255	intron-variant	MYCBP2	GRCh38.p7	13:77221992	TGTTAATAGTTGTTA[A/T]ACTCTGTTGTTTAGG	23077
rs75684723	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77135067	TATAGTTTGTTTGAG[G/T]TGGGATCCAAATAAC	23077
rs75692080	snp	C/G	0.0345262	0.126772	intron-variant	MYCBP2	GRCh38.p7	13:77125583	TCCAATACATTTCTA[C/G]TAAGAAATTAGTTTC	23077
rs75693429	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77131724	ATATACGAACACACA[C/T]ATATATAAAATAACA	23077
rs75710357	snp	C/T	0.0655868	0.168795	intron-variant	MYCBP2	GRCh38.p7	13:77105803	AGAATCAGGATTTTT[C/T]TCCAGTGCTCATTTG	23077
rs75748267	snp	A/G	0.00914312	0.0669923	intron-variant	MYCBP2	GRCh38.p7	13:77120287	GTACCCGAAGTAAGC[A/G]AGCAGATGATACCCA	23077
rs75764975	snp	C/T	0.0663309	0.169604	intron-variant	MYCBP2	GRCh38.p7	13:77068243	AGTAGTGGTAATTAC[C/T]AACCCAAGGCAGCAC	23077
rs75778094	snp	A/G	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77248541	TCACTAATCACTGGA[A/G]AAATTCAAATCAAAA	23077
rs75800789	snp	C/T	0.0614824	0.164198	intron-variant	MYCBP2	GRCh38.p7	13:77240009	ATCTATAAACTCACC[C/T]GTCAGGAAAAAGCAT	23077
rs75801480	snp	A/T	0.00914312	0.0669923	intron-variant	MYCBP2	GRCh38.p7	13:77184321	GCTATTGATTTTTAC[A/T]GTAATTCTACTGTGG	23077
rs75802187	snp	A/G/T			intron-variant	MYCBP2	GRCh38.p7	13:77193590	AATTCTTAGGATTAC[A/G/T]TAGAGAGGACTGATA	23077
rs75830615	snp	A/G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77047007	ACTGCAGCCCTTGGG[A/G/T]TTTTTCAAGGAAAAA	23077
rs75836667	snp	C/T	0.0341408	0.126114	intron-variant	MYCBP2	GRCh38.p7	13:77283154	TACAGGGTGGTGAGT[C/T]TGATGCAATCATGCA	23077
rs75851769	snp	A/C	0.0217236	0.101931	intron-variant	MYCBP2	GRCh38.p7	13:77142919	AGTCCAAAATCTAGA[A/C]TACTTCTGGTGCCAA	23077
rs75888704	snp	C/T	0.0663309	0.169604	intron-variant	MYCBP2	GRCh38.p7	13:77123619	ACTGAGGCACAGAGA[C/T]ATTAGGTTAACTTGG	23077
rs75896226	snp	A/T	0.0154538	0.0865337	intron-variant	MYCBP2	GRCh38.p7	13:77205734	TTAAACATCATTTCA[A/T]GGAAGAATGCTTAAA	23077
rs75913481	snp	A/G	0.00795532	0.062565	intron-variant	MYCBP2	GRCh38.p7	13:77105022	AGCTATTGTTAAAAT[A/G]TCAGTTAGGAGGGTG	23077
rs75930936	snp	A/G	0.5	0	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77080944	AGACTCCATCTCAGA[A/G]AAAAAAAAAAAAGCT	23077
rs75931929	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77102024	ATTTTTCTAACTTTA[A/T]AGGAAACCTGAAGAA	23077
rs75961986	snp	A/C	0.0256215	0.110247	intron-variant	MYCBP2	GRCh38.p7	13:77221395	TTAAAAGCTGACATG[A/C]ACACCTTCCCTCTCA	23077
rs75986452	snp	A/G	0.00438332	0.0466095	intron-variant	MYCBP2	GRCh38.p7	13:77177519	TAGAGATAGGGTTTT[A/G]CCATATTGCCTAGGC	23077
rs76035588	snp	A/T	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77059060	ATCACCAAAATGCAG[A/T]TTTTTTTTTTTTTTA	23077
rs76040514	snp	A/C	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77315361	AAGAAAAGAAAAAAA[A/C]CCGATTACAGACCAA	23077
rs76046348	snp	C/T	0.186737	0.241863	intron-variant	MYCBP2	GRCh38.p7	13:77284290	CAAGAAGGAATGGGA[C/T]AGCCACACACTTAGG	23077
rs76052618	snp	A/G	0.0637235	0.166737	intron-variant	MYCBP2	GRCh38.p7	13:77323710	TCTGCAATACTGCCT[A/G]GCACAGAGCAGGCAC	23077
rs76076778	snp	A/T	0.0158469	0.0875917	intron-variant	MYCBP2	GRCh38.p7	13:77054419	GTATTAATTAGCAGC[A/T]GTGTAAGGGATGCAA	23077
rs76095813	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77307841	CCTGCCCCCTGTCCC[A/G]CCAGCTTCTAGAACC	23077
rs76113738	snp	G/T	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77157105	AGTTAATTTTTTTTT[G/T]AGATAGGGTCTTGCT	23077
rs76168093	snp	G/T	0.00150202	0.0273634	intron-variant	MYCBP2	GRCh38.p7	13:77161997	AAAATATGTCAATAT[G/T]TAGTTTAGTTTAATT	23077
rs76185719	snp	A/T	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77201811	GGGTACACAATGAAA[A/T]GAAGGCAGAAATAAA	23077
rs76255587	snp	C/T	0.0260105	0.111035	intron-variant	MYCBP2	GRCh38.p7	13:77214695	TTATACAAACCTAGA[C/T]GGTATATCTACTACA	23077
rs76290235	snp	A/C	0.0337553	0.125452	intron-variant	MYCBP2	GRCh38.p7	13:77047704	ACCTTCAATCAGATA[A/C]AGGACAAGACCTGGG	23077
rs76314932	snp	C/T	0.0126979	0.078662	intron-variant	MYCBP2	GRCh38.p7	13:77285103	GTTATCTTAAGAATG[C/T]CTGATATTTCATTTA	23077
rs76340465	snp	A/C	0.0146672	0.084371	intron-variant	MYCBP2	GRCh38.p7	13:77144240	AGTCATGAGGGCTAC[A/C]GTGCCTGGGCGGACA	23077
rs76340999	snp	C/T	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77089650	GATCATGTAACTGTT[C/T]TTTTTTTTTTTTTAA	23077
rs76348904	snp	G/T	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77054618	CTTTTTTTTTTTTTT[G/T]GAGACAGGGTCTCAC	23077
rs76352716	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77089881	AGGTCAATTTATTCT[C/T]GAACAATCACTGAAT	23077
rs76355063	snp	A/T	0.0614824	0.164198	intron-variant	MYCBP2	GRCh38.p7	13:77206580	AATTACATATAAATT[A/T]AAATACTCTAAAAAA	23077
rs76384479	snp	A/C/G	0.0142736	0.0832652	intron-variant	MYCBP2	GRCh38.p7	13:77223608	CATGCAATTTAAGAA[A/C/G]CTGATGAGGCAGTTC	23077
rs76400406	snp	A/G	0.0614824	0.164198	intron-variant	MYCBP2	GRCh38.p7	13:77261453	TGAGGAAAAAAAAGG[A/G]CATCAATATTTTATT	23077
rs76408768	snp	C/T	0.00223495	0.0333538	intron-variant	MYCBP2	GRCh38.p7	13:77097357	TATACGTACATTCAA[C/T]AGTATCATTTACCTG	23077
rs76432865	snp	C/T	0.0130921	0.0798413	intron-variant	MYCBP2	GRCh38.p7	13:77182827	TGAGTGTAGATACCA[C/T]GTGTCTTGTTTCCAA	23077
rs76442421	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77055995	CATGAAAATTCCATT[C/T]TATTAGCTTTATATT	23077
rs76454430	snp	C/T	0.0064721	0.0565169	intron-variant	MYCBP2	GRCh38.p7	13:77166562	AATGTCACCTGAGGT[C/T]AACAGGCAAAGTGAC	23077
rs76473008	snp	A/G	0.0460142	0.144533	intron-variant	MYCBP2	GRCh38.p7	13:77154173	TCCAGCTAATATAAT[A/G]TGATATTAATACATT	23077
rs76478651	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77116645	ATGATTCAGAAAATT[A/G]CTAATTGAAACATAG	23077
rs76514084	snp	A/G	0.00953873	0.0683987	intron-variant	MYCBP2	GRCh38.p7	13:77251807	TCCAAGGTCTTCAGA[A/G]GAACAAAACTCAGCA	23077
rs76535005	snp	C/T	0.00676609	0.0577691	intron-variant	MYCBP2	GRCh38.p7	13:77306502	GGGGAGGACTATAAA[C/T]AAAGCTACCTTGGCA	23077
rs76537252	snp	C/T	0.00636936	0.0560724	intron-variant	MYCBP2	GRCh38.p7	13:77239559	GGTCATTGGATCAAA[C/T]CGCAAAGTGCAAACA	23077
rs76604541	snp	A/T	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77280993	GAATTTTTAATATTT[A/T]GCTATGGATTATTGC	23077
rs76605892	snp	G/T	0.00716266	0.059414	intron-variant	MYCBP2	GRCh38.p7	13:77158209	ATAGGCCTTTACGGA[G/T]AAATCATTTTCTCCA	23077
rs76608411	snp	A/G	0.029116	0.117091	intron-variant	MYCBP2	GRCh38.p7	13:77054169	GTGGCAGGTCAGAGT[A/G]AAATATGCAGGGGGA	23077
rs76626802	snp	C/T	0.00914312	0.0669923	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77080427	GAAAAAAATTCTAAA[C/T]GAGGTAGAAGAAAGG	23077
rs76628406	snp	A/G	0.000235337	0.010845	intron-variant	MYCBP2	GRCh38.p7	13:77118551	ATTAACATCCAAAAT[A/G]GCAAAGTAAATGGTG	23077
rs76650130	snp	A/C	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77134583	AACAACAAAAATAAC[A/C]AAAAAAAAAAGGAAA	23077
rs76687585	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77073024	CATACCATGCTATTC[A/T]TCTGTTTAAAGCATA	23077
rs76712682	snp	C/T	0.0704125	0.17392	intron-variant	MYCBP2	GRCh38.p7	13:77116109	ATGTTTCCTTCTCTG[C/T]AAAACAGACATAAGA	23077
rs76726325	snp	A/G	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77093588	TTTCCATCTTCCAGT[A/G]TTTTGGTGAATAAGC	23077
rs76744435	snp	C/T	0.0028112	0.0373858	missense	MYCBP2	GRCh38.p7	13:77185330	TTCTGGTTTTTCCAA[C/T]ACACTCTGCTAATTT	23077
rs76751678	snp	A/G	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77130984	ACAACATGTACAATG[A/G]TATTTTAAAATGATG	23077
rs76751964	snp	G/T	0.0618563	0.164627	intron-variant	MYCBP2	GRCh38.p7	13:77060451	AATTAAATTGATTCG[G/T]ATTTACACCTAACTC	23077
rs76770405	snp	G/T	0.0637235	0.166737	intron-variant	MYCBP2	GRCh38.p7	13:77284139	AACTCAATTTATTAG[G/T]AACTAAATAATAATT	23077
rs76794457	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77099433	ATTTCCAGCAGAGTG[A/G]TACCTCGCATCCTTA	23077
rs76799921	snp	C/T	0.0614824	0.164198	intron-variant	MYCBP2	GRCh38.p7	13:77242801	TGGCACAGTTCTTAA[C/T]ATGGCTGACTTATGC	23077
rs76801435	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77286844	TCTTAAATATACCAA[C/T]ACTTAAACAGAACAG	23077
rs76925591	snp	C/T	0.0275645	0.114116	intron-variant	MYCBP2	GRCh38.p7	13:77178342	CAGAGCTCTAGAAAT[C/T]CTGCAGAGATAGGTG	23077
rs76948027	snp	A/T	0.00914312	0.0669923	intron-variant	MYCBP2	GRCh38.p7	13:77321285	AGTTAGGAAACTAAT[A/T]CATTTCACATTTCTA	23077
rs76965947	snp	C/T	0.00914312	0.0669923	intron-variant	MYCBP2	GRCh38.p7	13:77218511	TGGCTGGTTGTGAAT[C/T]CTGGCTCCCCAACTT	23077
rs76971183	snp	A/G	0.0111196	0.0737302	intron-variant	MYCBP2	GRCh38.p7	13:77248415	TTCCTAAAACTCATC[A/G]ACAACAACAAAAGAA	23077
rs76980261	snp	G/T	0.158632	0.232706	intron-variant	MYCBP2	GRCh38.p7	13:77170822	CCTCATGATCTGCCT[G/T]CCTCGGCCTCCCAAA	23077
rs77007972	snp	A/T	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77059061	TCACCAAAATGCAGA[A/T]TTTTTTTTTTTTTAA	23077
rs77025939	snp	A/G	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77114888	AACTATTCAGCCTCT[A/G]GAACAGTAGGTAGAA	23077
rs77037763	snp	A/G	0.0333695	0.124785	intron-variant	MYCBP2	GRCh38.p7	13:77180456	CAAATCTTTCTGGTT[A/G]TATGTGGAGCCACTT	23077
rs77066362	snp	C/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77094927	CAGGATTTTGTTATA[C/T]TCATACATTCAGGGC	23077
rs77081743	snp	A/G	0.0111196	0.0737302	intron-variant	MYCBP2	GRCh38.p7	13:77265881	TGTATCTTCAGGAAT[A/G]TATCAAGCAACATCT	23077
rs77087496	snp	A/C	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77261047	AGTTACATCAAGTCA[A/C]TGATATATATATAAA	23077
rs77100360	snp	C/T	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77057836	TTTCAATCAACTGCT[C/T]TTTTTTTTTTTTTTT	23077
rs77135978	snp	C/G	0.0185938	0.0946107	intron-variant	MYCBP2	GRCh38.p7	13:77125546	CCAGTAAAAATCTTA[C/G]GTGTCTGAATAGTGT	23077
rs77140803	snp	A/C	0.0481883	0.147553	missense	MYCBP2	GRCh38.p7	13:77051098	CCAAAACAGAAAAAA[A/C]CAGCCACTGAACAGC	23077
rs77162960	snp	C/T	0.00835141	0.0640778	intron-variant	MYCBP2	GRCh38.p7	13:77108158	TCCACATGATCTGAA[C/T]GTGGAAAGAAGATGG	23077
rs77195856	snp	C/G	0.5	0	missense	MYCBP2	GRCh38.p7	13:77061783	TCATCATGGTTATCA[C/G]ACATAGGCTAAAATA	23077
rs77201999	snp	C/T	0.0225045	0.103662	intron-variant	MYCBP2	GRCh38.p7	13:77299577	CATTTGCTAGTAATA[C/T]AACACACCATTATAT	23077
rs77241178	in-del	-/TTT			intron-variant	MYCBP2	GRCh38.p7	13:77089661	TGTTTTTTTTTTTTT[-/TTT]AAATCGATTAAGGGC	23077
rs77244118	snp	C/G	0.0603597	0.1629	intron-variant	MYCBP2	GRCh38.p7	13:77255842	TTGTTAATTTATACA[C/G]CATTAATCCTCGAAA	23077
rs77260767	snp	A/C	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77111698	TGCAATTAACCTTAG[A/C]TTAAACCCTACTCAG	23077
rs77276886	snp	A/G	0.0569829	0.158885	intron-variant	MYCBP2	GRCh38.p7	13:77182770	TTCACGAAGGAGGGC[A/G]GGGAGGCCTAGGACT	23077
rs77280083	snp	C/T	0.0341408	0.126114	intron-variant	MYCBP2	GRCh38.p7	13:77221253	TTGAGCATATTGCTA[C/T]AATATTATTACCTGA	23077
rs77293643	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77158686	CTCCTGGCCTCAAGT[A/T]ATCCTCCCACCTTGC	23077
rs77321199	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77208758	GATACAGAGTATGAC[A/C]ATCCTTTTTCCTGTA	23077
rs77385622	snp	A/G	0.00716266	0.059414	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77085575	CCATCAACAGGTGGA[A/G]TTTATTTCTCAGTCT	23077
rs77392480	snp	C/G	0.0547245	0.156101	intron-variant	MYCBP2	GRCh38.p7	13:77302103	ATAATTGGAATCCCA[C/G]AAAGAGAGAAAAAAG	23077
rs77434767	snp	C/T	0.00636936	0.0560724	intron-variant	MYCBP2	GRCh38.p7	13:77143474	CTTATTATTAGTGGC[C/T]CTCCTGGATTCTCAG	23077
rs77525720	snp	C/T	0.0240643	0.107019	intron-variant	MYCBP2	GRCh38.p7	13:77114503	CAAGCTAAGTAAACA[C/T]AGTACTTTAGTGTGT	23077
rs77543341	snp	G/T	0.0329836	0.124112	intron-variant	MYCBP2	GRCh38.p7	13:77181337	CTTTATTTTCTTATT[G/T]TTCTATCTTAGAAAT	23077
rs77548353	snp	C/T	0.0329836	0.124112	intron-variant	MYCBP2	GRCh38.p7	13:77260878	AAACTCCTGGAGGGC[C/T]CAATCTCTAAATTAG	23077
rs77561524	snp	C/T	0.0271762	0.113356	intron-variant	MYCBP2	GRCh38.p7	13:77256523	TTCCTAATTCACAAA[C/T]ATAACGTCAAAGAGC	23077
rs77570008	snp	C/G	0.0360663	0.129354	intron-variant	MYCBP2	GRCh38.p7	13:77250266	AGCCTTAAAGAAAAG[C/G]CCTGTTATATATGAC	23077
rs77575542	snp	A/C			missense	MYCBP2	GRCh38.p7	13:77097654	AAAGAGATGTCTTCC[A/C]AAAAAGCCACTAAAT	23077
rs77595208	snp	C/T	0.0772408	0.180705	intron-variant	MYCBP2	GRCh38.p7	13:77278721	TATTAATTATATTCA[C/T]TTTTAAATGCTTCAC	23077
rs77599787	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77243345	TGGCTAGGCATGGTG[A/G]CCCACACCTGTAATC	23077
rs77616957	snp	C/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77214409	GAGAAACTGAATGAA[C/T]AAACTATCATATATA	23077
rs77633146	snp	G/T	0.0256215	0.110247	intron-variant	MYCBP2	GRCh38.p7	13:77226044	CTGCCCATAAGTATT[G/T]TGAAACTCAACTGAA	23077
rs77644830	snp	C/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77117539	ACAAATAACTTAGAC[C/T]TAAGTGTGAATGTAC	23077
rs77672507	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77285617	CATGGAGAAACCCCA[G/T]CTCTAATAAAAATAC	23077
rs77682582	snp	A/C	0.0614824	0.164198	intron-variant	MYCBP2	GRCh38.p7	13:77142744	AAGTTGAGCATCTCT[A/C]ATCTGAAAACCCCAA	23077
rs77717774	snp	C/T	0.0509478	0.151255	intron-variant	MYCBP2	GRCh38.p7	13:77188610	CTCAAGTAGTAATCA[C/T]GCTTTTTTGGGCCAG	23077
rs77750160	snp	A/G	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77219923	ATTCTTGTATTTTTC[A/G]TAGAGACCCCATGTC	23077
rs77775046	snp	A/C/T	0.00716713	0.0594884	intron-variant	MYCBP2	GRCh38.p7	13:77215056	CATTACCTCCAAGTA[A/C/T]GGAATGAAAGGTGTG	23077
rs77806805	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77096676	ATCAATTAAATGATG[C/T]CCCAAATATGAGAGA	23077
rs77822043	snp	A/G	0.00755907	0.0610114	intron-variant	MYCBP2	GRCh38.p7	13:77319226	TGATAGTCAGTAGGC[A/G]AGAGAGGAGGAGCTG	23077
rs77831696	snp	A/T	0.0168055	0.0901129	intron-variant	MYCBP2	GRCh38.p7	13:77130632	AAAGTGAAAAACATA[A/T]TGCAGAGCATTTTGA	23077
rs77836204	snp	A/G	0.0337553	0.125452	intron-variant	MYCBP2	GRCh38.p7	13:77104223	TAAACTAGACATAAC[A/G]CACACTTTTCTTAAA	23077
rs77838585	snp	A/G	0.0360663	0.129354	intron-variant	MYCBP2	GRCh38.p7	13:77299819	TATCCATCAGATTTG[A/G]AAGAATTGTGGTTGA	23077
rs77884242	snp	C/T	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77049330	GGAGAAACAGTAAAA[C/T]AATTTTTATTTGACA	23077
rs77912992	in-del	-/AAGAA			intron-variant	MYCBP2	GRCh38.p7	13:77055144	GGTTAAAAAAAAAAA[-/AAGAA]GAAGTAGTTAAAGAT	23077
rs77914018	snp	A/C	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77197609	AAGAGAATGCATATA[A/C]GAATATGTGAAGAAA	23077
rs77938935	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77286847	TAAATATACCAATAC[C/T]TAAACAGAACAGAGT	23077
rs77947105	snp	C/G	0.115438	0.210697	intron-variant	MYCBP2	GRCh38.p7	13:77273974	TCCTATCAAGTAATA[C/G]ACTACTTGTCATACT	23077
rs78000342	snp	C/T	0.0337553	0.125452	intron-variant	MYCBP2	GRCh38.p7	13:77189543	TACCAGAAAGAAAGA[C/T]AGGGAGATAGAATCA	23077
rs78003014	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77131513	ACACACACACACACA[A/C]ACAAACACACACACA	23077
rs78012799	snp	C/T	0.0341408	0.126114	intron-variant	MYCBP2	GRCh38.p7	13:77154220	ACAAATCACTTCTTC[C/T]AGATAGTATTTAGAG	23077
rs78015623	snp	C/T	0.0850919	0.187897	intron-variant, downstream-variant-500B	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087994	CTCACATGTTGCCCA[C/T]GCTGGTCTCAAACTC	23077
rs78023615	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77276684	TTTTTTTTGGTAGAG[A/T]TGAGGTCTCATTCTG	23077
rs78025576	snp	C/T	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77268992	GGAACTTGGGCTTCA[C/T]TGTTCAGGTAGGTAC	23077
rs78052178	snp	C/T	0.00993419	0.0697739	intron-variant	MYCBP2	GRCh38.p7	13:77266483	GATCACACTTTTTTA[C/T]AAGTATGGACATATA	23077
rs78092558	snp	C/T	0.0256215	0.110247	intron-variant	MYCBP2	GRCh38.p7	13:77248767	CCACTTCTGGGTATA[C/T]GCCCAAAAGAACTGA	23077
rs78097360	snp	C/T	0.0310518	0.120672	intron-variant	MYCBP2	GRCh38.p7	13:77299207	CCTAAAGACAAGTTA[C/T]AACTGACTCAAATTT	23077
rs78105111	snp	C/G/T	0.0049398	0.0494933	intron-variant	MYCBP2	GRCh38.p7	13:77190370	ATACCAAAAACAACA[C/G/T]GATCATTACAGGAAA	23077
rs78105595	snp	A/G	0.0130921	0.0798413	intron-variant	MYCBP2	GRCh38.p7	13:77168194	ACACTATACTTGTAG[A/G]AAGATTTAAGAACAA	23077
rs78111222	snp	A/G	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77282102	AAGAGAGGAGGAGAA[A/G]GCTAAGATGGAGAAT	23077
rs78111387	snp	G/T	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77258155	GGTCTAAGCACAAAG[G/T]AGTCCATAAATAATT	23077
rs78112389	snp	A/C	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77188072	CGAGACTCTGCCTCA[A/C]CAAAAAAAAAAAAAA	23077
rs78142496	snp	A/T	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77153087	AAAAAAAAAAAAAAA[A/T]ATCTGCTGTATTCAC	23077
rs78147268	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77084321	CCAATGTAAGCCCAT[C/G]AAACTTTTTAAACTA	23077
rs78152703	snp	C/T	0.104149	0.203046	intron-variant	MYCBP2	GRCh38.p7	13:77197605	TCAAAAGAGAATGCA[C/T]ATACGAATATGTGAA	23077
rs78186824	snp	G/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77194981	GGTTATGAAATTAAG[G/T]GAAAATAAGAATTAT	23077
rs78187980	snp	C/T	0.0217236	0.101931	intron-variant	MYCBP2	GRCh38.p7	13:77100324	GCTGGAGAATCTGCC[C/T]CAGTCTTTGTCAAGG	23077
rs78228335	snp	A/C	0.0146672	0.084371	intron-variant	MYCBP2	GRCh38.p7	13:77309082	GTTATCTAATCCAAA[A/C]GATTAATTATTTGTC	23077
rs78229620	snp	C/T	0.0256215	0.110247	intron-variant	MYCBP2	GRCh38.p7	13:77324017	CTCCATTTAGCCTCC[C/T]ATATTTGCATATCCC	23077
rs78239717	snp	A/C			missense	MYCBP2	GRCh38.p7	13:77068591	TTCTCGCTGCTTCAC[A/C]CAGCCTCTCCTAGAG	23077
rs78263587	snp	C/T	0.0603597	0.1629	intron-variant	MYCBP2	GRCh38.p7	13:77226233	TGCTTTCACTCCTTC[C/T]TTCCTCCTCCCTTCT	23077
rs78310772	snp	C/T	0.0197687	0.0974348	intron-variant	MYCBP2	GRCh38.p7	13:77174745	TAAGGTAAGTATCAT[C/T]ACTATCCCTATTTTA	23077
rs78322020	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77218233	TGAAAAACTGGTGCT[A/G]CATTTATTTTTAATC	23077
rs78323561	snp	A/G	0.0614824	0.164198	intron-variant	MYCBP2	GRCh38.p7	13:77257054	TACTATTTAACCATA[A/G]AAAACACTGAGATCC	23077
rs78325821	snp	C/T	0.0614824	0.164198	intron-variant	MYCBP2	GRCh38.p7	13:77182239	TTCAAAGGGAGATGC[C/T]AAAAAGGCCCCAATT	23077
rs78333014	snp	A/C	0.5	0	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77329021	ATAGATGTTGGCTGA[A/C]TGAATGAATGTTGCT	23077
rs78354543	snp	A/G	0.0252325	0.109451	intron-variant	MYCBP2	GRCh38.p7	13:77132895	ACTAGCTCACATTTT[A/G]CAGATTCCACATCTT	23077
rs78359926	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77108643	AGAGACAACGCTTAC[A/G]CAGCACAAAGACAGC	23077
rs78378439	snp	A/G	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77177592	CTCTCAAAGAGCTGA[A/G]ATTACAGGTGTGAGC	23077
rs78387739	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77281994	ATTGTTTGTATAAAG[C/T]AAATATTTGGTACAG	23077
rs78397431	snp	A/G	0.00760872	0.0612084	intron-variant	MYCBP2	GRCh38.p7	13:77144416	AGTTATTTGAAGTAA[A/G]TAGTAGCTCATGGCT	23077
rs78449361	snp	G/T	0.0329836	0.124112	intron-variant	MYCBP2	GRCh38.p7	13:77211523	ATGCTCCTAATCTCT[G/T]GCTATACCACTCTAT	23077
rs78495089	snp	G/T	0.5	0	utr-variant-3-prime	MYCBP2	GRCh38.p7	13:77044901	CTGTCCTAACACAAT[G/T]TTTTTTTTTTTTTTA	23077
rs78505755	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77134245	TTCTCAGCCGGGTGC[A/T]GTGGCTCACGTCTTT	23077
rs78521360	in-del	-/T	0.0614824	0.164198	intron-variant	MYCBP2	GRCh38.p7	13:77159060	TTTTTTCATAGAAAA[-/T]AATTACATTTCTAGT	23077
rs78532309	snp	C/T	0.0146672	0.084371	intron-variant	MYCBP2	GRCh38.p7	13:77221855	CTGCAGCTACCAAAC[C/T]CTAGGGATGCTCAAA	23077
rs78557367	snp	C/T	0.00795532	0.062565	intron-variant	MYCBP2	GRCh38.p7	13:77102607	TTTGTCAATTGTCAA[C/T]AGTTTAAACATTTCT	23077
rs78563384	in-del	-/AA			intron-variant	MYCBP2	GRCh38.p7	13:77055144	GGTTAAAAAAAAAAA[-/AA]GAAGAAGTAGTTAAA	23077
rs78572426	snp	A/G	0.00835141	0.0640778	intron-variant	MYCBP2	GRCh38.p7	13:77177366	TTTTGAGACAGGGTC[A/G]GGTCTCACTCTGCTG	23077
rs78588845	snp	G/T	0.00993419	0.0697739	intron-variant	MYCBP2	GRCh38.p7	13:77274698	TATCTCATCATCATC[G/T]TTCCAATCCATGCTA	23077
rs78609216	in-del	-/G	0.0345262	0.126772	intron-variant	MYCBP2	GRCh38.p7	13:77214016	GTTAGAAAAAGCACA[-/G]GGAAACACATGCCCC	23077
rs78612904	snp	A/G	0.0486741	0.148216	intron-variant	MYCBP2	GRCh38.p7	13:77175229	TGCGCTACTGTGCCC[A/G]GCAATAAGGGATTTT	23077
rs78635110	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77285614	CAACATGGAGAAACC[C/T]CATCTCTAATAAAAA	23077
rs78640596	snp	A/G			intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77074251	TCTTCTCAATGAATC[A/G]TAGTAGAACAATTGA	23077
rs78654836	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77171146	GGGTACCCCAGAGTT[C/T]TGGGTGGATAGCGAT	23077
rs78702450	snp	C/G	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77154700	TTGAGAAATTCATCA[C/G]TGAATACACAATATA	23077
rs78729180	snp	C/T	0.0667028	0.170006	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77084725	GAAGCTAAGAATCTG[C/T]TCAGTTCTCAGCTTA	23077
rs78740511	snp	A/C	0.0263992	0.111815	intron-variant	MYCBP2	GRCh38.p7	13:77136366	CAACTCTTTAACTAT[A/C]GTGCATTCACTATAT	23077
rs78741973	snp	C/T	0.00993419	0.0697739	intron-variant	MYCBP2	GRCh38.p7	13:77305804	ATATGATCACTTCAA[C/T]AGAAACAGAAAAAGT	23077
rs78742695	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77148225	ATTTATTTCGGATAT[A/T]GAATTCATAATGAGA	23077
rs78755726	snp	A/C	0.0158469	0.0875917	intron-variant	MYCBP2	GRCh38.p7	13:77188193	AGGATACTTTTATCT[A/C]ATTCCTACCAGGAAT	23077
rs78774979	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77129548	TTCTTTAAATGAGGA[C/T]GTATTTGTTCTAATA	23077
rs78841403	snp	A/T	0.00914312	0.0669923	intron-variant	MYCBP2	GRCh38.p7	13:77132071	ATTACAATCTTAATT[A/T]AACTGTTTTAATCTC	23077
rs78866616	snp	A/G	0.0263992	0.111815	intron-variant	MYCBP2	GRCh38.p7	13:77120310	GATACCCAATCCTAT[A/G]AGATAGGCTAGTCCA	23077
rs78874804	snp	G/T			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087261	GGTAGAAATGAGGCT[G/T]AACTCAGGCTCCTAG	23077
rs78932558	snp	A/G	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77256969	CACAATAGCAAAGAT[A/G]TGGAATCAACCTAAG	23077
rs78940355	snp	A/G	0.0614824	0.164198	intron-variant	MYCBP2	GRCh38.p7	13:77143289	AGTGGAGTAGGTGGA[A/G]AAGATCTGCTTTCAA	23077
rs78946390	snp	G/T	0.030665	0.119967	intron-variant	MYCBP2	GRCh38.p7	13:77224762	ACACTTAAAAATTCG[G/T]ATAAATGCCATTTAA	23077
rs78992190	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	MYCBP2	GRCh38.p7	13:77044645	TTTTTTAAACAATAC[C/T]TCCCACAGTGGTAGA	23077
rs78998431	snp	C/T	0.126219	0.217206	intron-variant	MYCBP2	GRCh38.p7	13:77050370	TAAAATTCTCTCCTA[C/T]GGTTGCACGGACCTC	23077
rs79022785	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77134255	GGTGCAGTGGCTCAC[A/G]TCTTTAATCCCAGTC	23077
rs79076697	snp	G/T	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77049661	TTGCTTTTTTTTTTT[G/T]AAACAGCTCTGTCGC	23077
rs79083193	snp	A/C	0.00478085	0.0486577	intron-variant	MYCBP2	GRCh38.p7	13:77154063	AATTAGCTATTACTG[A/C]ATAAAGATTTTAACA	23077
rs79090275	snp	C/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77068223	CATACTATTCAAATG[C/G]TAATAGTAGTGGTAA	23077
rs79098688	snp	A/G	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77113078	CACTGCCTGACACGT[A/G]GGTGGACTCAATAAA	23077
rs79181378	snp	A/C	0.0236746	0.106192	intron-variant	MYCBP2	GRCh38.p7	13:77107115	TAGAATGATGGGAAC[A/C]GTGTTGCTGACTTTC	23077
rs79189048	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77073023	ACATACCATGCTATT[C/T]ATCTGTTTAAAGCAT	23077
rs79200217	snp	C/G	0.0379877	0.132479	intron-variant	MYCBP2	GRCh38.p7	13:77105752	CTTTTTTGGGTATCA[C/G]TAAGTTTAAGAGAAT	23077
rs79217148	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77091564	CTGTCTTGCCTCCTG[C/T]AGGATGGTTAGCAAC	23077
rs79225062	in-del	-/AA			intron-variant	MYCBP2	GRCh38.p7	13:77053150	CTCAAAAAAAAAAAA[-/AA]GGCAAATTTGATAAT	23077
rs79231242	snp	C/G	0.0138799	0.0821421	intron-variant	MYCBP2	GRCh38.p7	13:77271496	ATACTCATATGGTTT[C/G]GTTGTGTTCCCACTC	23077
rs79231543	snp	C/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77061557	CTCAACCAAGGTCTT[C/T]GATTCCAAAGTCCAC	23077
rs79245939	snp	G/T	0.0225045	0.103662	intron-variant	MYCBP2	GRCh38.p7	13:77285163	CCCTAGGAATCCATT[G/T]TTCTTGTTTATGCAA	23077
rs79265272	snp	G/T	0.0752113	0.178743	intron-variant	MYCBP2	GRCh38.p7	13:77306490	GTCTTCACATGGGGG[G/T]AGGACTATAAATAAA	23077
rs79281940	snp	C/T	0.0205511	0.0992634	intron-variant	MYCBP2	GRCh38.p7	13:77141262	AATCTTATCTGACAA[C/T]ATCCAATCAGAATAC	23077
rs79287012	snp	G/T	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77302340	AAGGAACAATAAAAT[G/T]GATAGTTTCCATTCT	23077
rs79314178	in-del	-/NAA			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228512	CCCTGTCTCAAAAAA[-/NAA]AAAAAAAAAATCTGT	23077
rs79331866	snp	C/T	0.00953873	0.0683987	intron-variant	MYCBP2	GRCh38.p7	13:77198687	ATAGGTGTGGTAACA[C/T]ATGACTCTCAATGAT	23077
rs79332069	snp	C/G	0.0614824	0.164198	intron-variant	MYCBP2	GRCh38.p7	13:77223584	CAAGTTTATTTCTCA[C/G]GCAAGAAGCATGCAA	23077
rs79336758	snp	A/G	0.0138799	0.0821421	intron-variant	MYCBP2	GRCh38.p7	13:77174786	ATCTGAGGTTCAGAG[A/G]AGTTAAGTAACTTGT	23077
rs79353704	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77143586	GGTGTGGCCCATAAT[A/G]GGACTTTTCAGACTC	23077
rs79393692	snp	A/T	0.5	0	intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77325674	TTTCCCCTTTTCCCT[A/T]CAAAACCCTCTCTAC	23077
rs79395926	snp	C/T	0.00716266	0.059414	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77294337	CCTCTTACTCATCTT[C/T]GTATCCCAAACATCC	23077
rs79425400	snp	A/G	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77272634	AAATAATTAAGGACC[A/G]TAAAAAGGGACAAAA	23077
rs79427491	snp	C/T	0.0189856	0.0955633	intron-variant	MYCBP2	GRCh38.p7	13:77131589	TTTAGTCTAAAGATA[C/T]GAACATTCAGGAAAA	23077
rs79445702	snp	C/T	0.0509478	0.151255	intron-variant	MYCBP2	GRCh38.p7	13:77135152	TAGACACAAACAGTG[C/T]TGAAGGCAACTTTTC	23077
rs79448613	snp	C/T	0.0138799	0.0821421	intron-variant	MYCBP2	GRCh38.p7	13:77106735	TTCCTTTTTTTTCTT[C/T]CCAATTTTTTTCTTT	23077
rs79463642	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77102023	CATTTTTCTAACTTT[A/T]AAGGAAACCTGAAGA	23077
rs79480195	snp	A/G	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77058147	GCCCGGCCTCAATCA[A/G]TGTTTATTTGACAAA	23077
rs79524295	snp	A/G	0.0271762	0.113356	intron-variant	MYCBP2	GRCh38.p7	13:77299075	GGTATTTGAGCAACA[A/G]GAATACATAACTACT	23077
rs79548290	snp	C/T	0.0111196	0.0737302	intron-variant	MYCBP2	GRCh38.p7	13:77271035	TCATTTCTAGGAGTT[C/T]GATTTGTTTTTTTTC	23077
rs79548492	snp	C/T	0.0256215	0.110247	intron-variant	MYCBP2	GRCh38.p7	13:77229431	GAGTTTAATCATAAA[C/T]AAGGCTCATGCATTT	23077
rs79556351	snp	C/T	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77048073	AATGAGAGACTGTTA[C/T]ATCTTGGTGCACTGC	23077
rs79593836	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77191221	GAACTGAAAAGTACT[C/T]TATACGTGAAAGTTA	23077
rs79598830	snp	A/G	0.0178098	0.0926698	intron-variant	MYCBP2	GRCh38.p7	13:77279249	TACAAGGAGCTTTTC[A/G]TCTTAGCCTTTTCTA	23077
rs79657547	snp	A/G	0.00835141	0.0640778	intron-variant	MYCBP2	GRCh38.p7	13:77198683	ACGAATAGGTGTGGT[A/G]ACATATGACTCTCAA	23077
rs79658721	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77077739	ACTTTATCTATATCA[A/T]CTGTAAGTGGAAACC	23077
rs79667502	snp	C/T	0.0329836	0.124112	intron-variant	MYCBP2	GRCh38.p7	13:77059354	GTTTGGGCTTGAGAG[C/T]CTTATTTGACCCATT	23077
rs79672481	snp	C/T	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77297588	AGAAAAATTTTAAGC[C/T]TAGGTCACTTGGAGG	23077
rs79678147	snp	A/T	0.116138	0.211142	intron-variant	MYCBP2	GRCh38.p7	13:77108709	TAAGATACTTTATTT[A/T]TTTTTTTTTTTTGAG	23077
rs79698158	snp	A/C/T	0.0592355	0.161582	intron-variant	MYCBP2	GRCh38.p7	13:77217964	GGACATCCCCTAGGT[A/C/T]AAAAAAAAAAAAAGT	23077
rs79703206	snp	A/C	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77154557	TGCAAAGGAGAAAAC[A/C]CAAGAAAGAAAATAC	23077
rs79752193	snp	C/T	0.0271762	0.113356	intron-variant	MYCBP2	GRCh38.p7	13:77127149	TACTCTCTAATATTG[C/T]ACAAATAAAAACGTC	23077
rs79774540	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77280151	AAGGTAAGTCAATTG[C/T]AGTTCTGATTAACAT	23077
rs79789387	snp	C/T	0.0138799	0.0821421	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77074263	ATCGTAGTAGAACAA[C/T]TGAACATCTATATGC	23077
rs79793712	snp	A/C	0.0618563	0.164627	intron-variant	MYCBP2	GRCh38.p7	13:77059826	AAAGAAATTAAAGAC[A/C]TATCTGAAGCCAAAT	23077
rs79866244	snp	C/G	0.119281	0.213102	intron-variant	MYCBP2	GRCh38.p7	13:77108685	CCAAAAACAGAAGTG[C/G]TTTTAGGATAAGATA	23077
rs79893521	in-del	-/GT			intron-variant	MYCBP2	GRCh38.p7	13:77089647	CCAGATCATGTAACT[-/GT]TTTTTTTTTTTTTTT	23077
rs79930730	snp	C/T	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77089649	AGATCATGTAACTGT[C/T]TTTTTTTTTTTTTTA	23077
rs79951076	snp	G/T	0.0256215	0.110247	intron-variant	MYCBP2	GRCh38.p7	13:77294838	TCCTTAGGGTAACTA[G/T]TCCTCCCTCATTTCA	23077
rs79957986	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77285943	GCTATTAGAGTAGGT[A/G]CAGTTAGGACATTGC	23077
rs79959280	snp	C/T	0.0667028	0.170006	intron-variant	MYCBP2	GRCh38.p7	13:77105828	CATTTGAAGTTAATA[C/T]TGTTTGCTTACTATA	23077
rs80001232	snp	C/T	0.0614824	0.164198	intron-variant	MYCBP2	GRCh38.p7	13:77242903	GAAGCATGAATACCC[C/T]GAATATTTTCCCATT	23077
rs80012196	snp	C/T	0.0263992	0.111815	intron-variant	MYCBP2	GRCh38.p7	13:77320116	GTCTTATAGCAAAAG[C/T]GCTAGGCATTTATAT	23077
rs80013713	snp	C/T	0.0158469	0.0875917	intron-variant	MYCBP2	GRCh38.p7	13:77290371	CTTGGACATTTACAC[C/T]AGAGAAATAAAAACT	23077
rs80039578	snp	C/T	0.00557542	0.0525036	intron-variant	MYCBP2	GRCh38.p7	13:77158205	TCAGATAGGCCTTTA[C/T]GGAGAAATCATTTTC	23077
rs80044312	snp	A/G	0.0134861	0.0810011	intron-variant	MYCBP2	GRCh38.p7	13:77264214	ATTTATAAATCTTCC[A/G]TAACCAAGGACCTGA	23077
rs80048581	snp	A/T	0.0345262	0.126772	intron-variant	MYCBP2	GRCh38.p7	13:77288602	TGACAAGGGCTGGAA[A/T]AGGATGGGCAAAAAA	23077
rs80058812	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77225805	GATCTGGTTATGGAT[A/G]AAACCTTATGTAATA	23077
rs80062212	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77134259	CAGTGGCTCACGTCT[A/T]TAATCCCAGTCTGTA	23077
rs80103339	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77290250	ATGAGGAGAAACTTA[C/T]ACATTGCTGATGGTC	23077
rs80121007	snp	A/T	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77059062	CACCAAAATGCAGAT[A/T]TTTTTTTTTTTTAAA	23077
rs80134907	snp	C/T	0.0584853	0.160693	intron-variant	MYCBP2	GRCh38.p7	13:77182759	CAATGATTTTTTTCA[C/T]GAAGGAGGGCGGGGA	23077
rs80143630	snp	A/G	0.00914312	0.0669923	intron-variant	MYCBP2	GRCh38.p7	13:77297585	AAGAGAAAAATTTTA[A/G]GCCTAGGTCACTTGG	23077
rs80144707	snp	C/T	0.0614824	0.164198	intron-variant	MYCBP2	GRCh38.p7	13:77244810	CAAAGAACTTAAACA[C/T]ATTTACAAGAAAACA	23077
rs80146913	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77286846	TTAAATATACCAATA[A/C]TTAAACAGAACAGAG	23077
rs80198095	snp	A/C	0.0256215	0.110247	intron-variant	MYCBP2	GRCh38.p7	13:77263431	GAGAAATTATTAGTC[A/C]ATTCCTTAGAATGGT	23077
rs80204129	snp	A/T	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77048058	GGCATTATCTCAGAC[A/T]ATGAGAGACTGTTAT	23077
rs80208414	snp	C/T	0.125528	0.21681	intron-variant	MYCBP2	GRCh38.p7	13:77071736	TTGAACTAACTGATA[C/T]TTATAGAACCCCTCA	23077
rs80223665	snp	C/G	0.5	0	missense	MYCBP2	GRCh38.p7	13:77263684	TTTCCAGATCGAATA[C/G]TGAGATACCACAGGC	23077
rs80233601	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77084090	CCACTTCAGAACAGT[C/T]ATTTAGGTTGTTTCC	23077
rs80274039	snp	A/T	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77047587	ATCCCCATATAACAT[A/T]AAAAGCAGTTGGGGA	23077
rs80276147	snp	A/C	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77143967	AATGCTATGAGGTAC[A/C]TGACTGTATAGATAT	23077
rs80315881	snp	A/G	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77063580	AAAAAAAAAAAAAAA[A/G]AGACAACTGTTTTCA	23077
rs80327140	snp	A/C	0.0279526	0.114869	intron-variant	MYCBP2	GRCh38.p7	13:77217613	GTCCAATTCTAACAA[A/C]GCTGTTAAATTCAAT	23077
rs80335169	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77095274	CTAATAAAGTGTAGG[C/T]CAAATACCGAACTAC	23077
rs111239264	snp	C/T	0.5	0	missense	MYCBP2	GRCh38.p7	13:77267886	GTGTTTCAGGGCTTA[C/T]CCTTATGGCTGTCAT	23077
rs111247542	snp	C/T	1.67147e-05	0.00289086	synonymous-codon, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77078839	CTGCTTTATTCTGCA[C/T]AAATCTTCTACTGCT	23077
rs111253288	snp	C/T	0.00953873	0.0683987	intron-variant	MYCBP2	GRCh38.p7	13:77131505	ACACACACACACACA[C/T]ACACACAAACAAACA	23077
rs111256048	snp	C/T	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77093746	CCTATCATCACTGCC[C/T]TGGTTCATGCTTATT	23077
rs111269915	snp	A/T	0.0659589	0.169201	intron-variant	MYCBP2	GRCh38.p7	13:77262839	GGCTTTAAAAATTTT[A/T]AATCTGTAATTTCAA	23077
rs111296062	snp	A/G	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77125514	GCTTGATTCTTTCAG[A/G]GAACTCAGTCTGAAA	23077
rs111313240	snp	C/T	0.0704125	0.17392	intron-variant	MYCBP2	GRCh38.p7	13:77139869	TTAGTCATTTTTTAA[C/T]GATAAAATAAATGAA	23077
rs111319604	in-del	-/T	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77112273	TTGCACTGGACTGTA[-/T]CCCCTCTTCTTTATA	23077
rs111388294	snp	A/G	0.0185938	0.0946107	intron-variant	MYCBP2	GRCh38.p7	13:77298323	TAACTCCCCACACTG[A/G]ATGAGTTTCCCTAAT	23077
rs111394444	snp	C/T	0.5	0	synonymous-codon	MYCBP2	GRCh38.p7	13:77263751	TTGCTGTAGAACAGG[C/T]TCAGTGCTTGTGGCA	23077
rs111396170	snp	G/T	0.0345262	0.126772	intron-variant	MYCBP2	GRCh38.p7	13:77276666	TGGGATTTTTTGGGG[G/T]TTTTTTTTTTGGTAG	23077
rs111403765	snp	G/T	0.0197687	0.0974348	intron-variant	MYCBP2	GRCh38.p7	13:77159613	TTCCCCCTTGCTGTT[G/T]TCCTTACAATATCTG	23077
rs111404634	snp	G/T	0.00914312	0.0669923	intron-variant	MYCBP2	GRCh38.p7	13:77300396	ATAAAGAGAGGAGTG[G/T]GCATATATTACAATA	23077
rs111442757	snp	A/G	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77272956	TTTCCCACCACTAAA[A/G]TGGTGATGAGCTTGT	23077
rs111454949	snp	G/T	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77134510	CTGAACTCCAGCTTG[G/T]GTGGCAGGGCAAGGT	23077
rs111455068	snp	A/G	0.5	0	synonymous-codon	MYCBP2	GRCh38.p7	13:77156130	GGTGGTAGGCCAACC[A/G]CAACGAATATCATCC	23077
rs111465775	snp	A/G	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77119335	GGTGATGCAGAAACT[A/G]GAAAATAGTATCTTT	23077
rs111467156	snp	G/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77105367	AAGGCTAGAGAGACT[G/T]GATTCCTAGGTATGA	23077
rs111469217	snp	A/G	0.0111196	0.0737302	intron-variant	MYCBP2	GRCh38.p7	13:77095191	ATACCTATTACCATA[A/G]AGTCATTATGTCAGT	23077
rs111475464	snp	A/G	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77181471	AAGGTGTGTGATTAA[A/G]CCGTTAGAGCAAAAA	23077
rs111479834	snp	A/G	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77195186	AGAAATCTTTCTCCA[A/G]CTCAGCTCTTATTCT	23077
rs111488895	snp	C/T	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77168722	GCATTACAATAATTG[C/T]TGGTTACTCTAATAA	23077
rs111493966	snp	A/G	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77095842	TTTAACACCTAACTA[A/G]TTAAATCTAAATGTA	23077
rs111496525	snp	A/G	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77067427	ATAAATGACACTTTT[A/G]TTATATACATGACCT	23077
rs111508032	snp	C/T	0.0107246	0.0724382	intron-variant	MYCBP2	GRCh38.p7	13:77048687	CCATCTACTCGCAGA[C/T]TGTAAAAATGGAGCA	23077
rs111548873	snp	A/G	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77055076	CCAAGGTAAGGAAGT[A/G]TTTATTAAGTAGGCA	23077
rs111551045	snp	C/T	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77090834	TATAAAAGAACTTAA[C/T]GGTTTTATTCAGGCT	23077
rs111558798	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77226377	TATAAAAATTTTTGT[C/T]TGGAATGTGTAAATA	23077
rs111596962	snp	A/C	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77224197	ATATTTTGTGACAAT[A/C]ATAATCACTCTCCTA	23077
rs111600531	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77312546	CCTGTAAAAAGTTAG[A/G]TATGCATACTGTAAT	23077
rs111603868	snp	C/G	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77322040	TGGTGCATGCCTGTA[C/G]TCCCAGCTACTGGAG	23077
rs111630085	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77294417	ATGAATGAACTTACT[C/T]ACATCACTGTTATCT	23077
rs111642157	snp	C/T	0.00358746	0.0422002	missense	MYCBP2	GRCh38.p7	13:77166442	GGTCCATATCCTGAA[C/T]TCTGAACAGTTCTGA	23077
rs111645024	snp	C/T	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77190925	TTATATAACTTCAAC[C/T]GATTTCAAATAGTTT	23077
rs111669948	snp	G/T	0.0479149	0.147179	intron-variant	MYCBP2	GRCh38.p7	13:77058086	ACCTCGTGATCCACC[G/T]GCCTCGGCCTCCCAA	23077
rs111672638	snp	A/G	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77321511	TCAAGGGTGATCAGT[A/G]TCTACTGAATAAAAT	23077
rs111676944	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77092825	AGTTAGGAGGCACTG[C/T]AAACAATAATCCAAG	23077
rs111683492	snp	A/T	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77314942	AAAAAATATTTTTTT[A/T]AAAAAAGGAGGGAGT	23077
rs111691082	snp	C/T	0.000153988	0.00877328	missense	MYCBP2	GRCh38.p7	13:77171537	CCTTAGAGGCTCGAA[C/T]GACAGTGCTTACAAC	23077
rs111705515	snp	A/C	0.0130921	0.0798413	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77292527	AGGGAAAGACACCAG[A/C]TTTAAAAAAAAAAGA	23077
rs111710729	snp	C/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77072419	CTAATGTAGTGCTTA[C/G]AAGAAAATAATAGCA	23077
rs111712731	snp	C/T	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77052226	TTCTTTGAGACGGGC[C/T]CTCACTCTGTTGCCC	23077
rs111722153	snp	A/C	0.00474123	0.0484576	intron-variant	MYCBP2	GRCh38.p7	13:77157891	TTTCAGAAATGAAGA[A/C]AGATGAAAGCCCTAA	23077
rs111723741	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77207956	CCCATCCCCCCACCA[A/T]GCCCCACCCGCCCCA	23077
rs111724751	in-del	-/T	0.0103295	0.0711199	intron-variant	MYCBP2	GRCh38.p7	13:77163050	TAGGCTGTATAGGTC[-/T]ACTTTTTCAAAGAGC	23077
rs111729842	snp	C/T	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77188377	ATTAGAAATTCAAAA[C/T]GCTATGATGTAATTT	23077
rs111730591	in-del	-/A	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77284238	TTAATCATGTTAAGG[-/A]AAAAAAAAAAAGAGT	23077
rs111738158	snp	C/T	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77058868	CGCGCGCCTGTAATC[C/T]CAGCTACTTAGGAAG	23077
rs111744353	snp	A/G	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77142482	ACATACAATTACATC[A/G]ATGTAAAGTACCTCT	23077
rs111747243	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77107977	ACATAAATGTTGGTA[C/T]ACTAAAAGAATTAGA	23077
rs111748216	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77137066	ATTAACAACCTCCGC[A/G]CTCACATTCCAGTGA	23077
rs111774023	in-del	-/A	0.00199481	0.0315187	intron-variant, nc-transcript-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087755	AAATCTTTTTTAATT[-/A]AAAAAAAATGCCTTA	23077
rs111854684	snp	C/G	0.030665	0.119967	intron-variant	MYCBP2	GRCh38.p7	13:77152851	CGGGCGAATCACAAG[C/G]TCAGGAGATCGAGAC	23077
rs111877092	snp	C/T	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77260715	ACTATTTGTTTATTT[C/T]CACAAAGGCCTGGGC	23077
rs111899664	snp	C/T	0.0103295	0.0711199	intron-variant	MYCBP2	GRCh38.p7	13:77116563	CAAAATTTAGAGACG[C/T]CCTGTTGCGAATAAG	23077
rs111923896	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77239023	TACTCGGGAGGCCGA[G/T]GCAGGAGAATCGCTT	23077
rs111941735	snp	C/T	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77163707	TTCAAATGGACCGCC[C/T]TTCCTTACTTTCCAT	23077
rs111969133	snp	A/G	0.5	0	missense, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77083174	AGAGTGGATGTTCAC[A/G]TACTCTTGTATCTTT	23077
rs111969799	in-del	-/AT/TA	0.5	0	downstream-variant-500B	MYCBP2	GRCh38.p7	13:77044459	ATATTTACCTACGAA[-/AT/TA]TATATATATATATAT	23077
rs111972013	snp	C/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77070334	CCTGCAGCCGGGGGA[C/G]TGCCTGTGGCCCAGG	23077
rs111981666	snp	A/G	0.0150606	0.0854603	intron-variant	MYCBP2	GRCh38.p7	13:77177503	TGCGTTGTATTTTTC[A/G]TAGAGATAGGGTTTT	23077
rs111998384	snp	C/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77109429	CCTCCTGCTGTACAG[C/G]TGGGTTCCTAACAGG	23077
rs112047202	snp	C/G	0.5	0	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291660	TAATCCCAGCTCCTC[C/G]GGAGCCTGAGGCAGG	23077
rs112077311	snp	A/G	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77319110	GTGCAGTTTGGGAAC[A/G]TGTGTGTGTGTGTGT	23077
rs112083604	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77210057	CTACTAAGGCCGGCC[A/G]CAAAAGGAAAGAAGT	23077
rs112115008	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77299998	ATTCAGTGATATAGA[C/T]CAATAGTTTCTCTAT	23077
rs112132093	snp	A/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77144826	TCAGATACAACCTCA[A/T]AGTTGCAATGTGATT	23077
rs112138190	snp	A/G	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77171085	AGATTCCAATGGAAA[A/G]ACTCATAGAGCTGAA	23077
rs112173340	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77120257	AAAGATCTAGCTTAA[A/G]TTAATGGAAATCAGG	23077
rs112189688	snp	A/G	0.00835141	0.0640778	intron-variant	MYCBP2	GRCh38.p7	13:77283421	ACAATGCTTTCTTGA[A/G]GGCAGGAATTATGTC	23077
rs112191845	snp	A/G	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77167957	AAAAACAAAGAATAC[A/G]GATTTTGAATACTCT	23077
rs112203623	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77139770	TTAAAATGTCATGAA[A/G]AACTATACCCATTTT	23077
rs112245465	in-del	-/TCTT	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77162435	TATTTTATTTATTGA[-/TCTT]TCTTTGATAGTTTAA	23077
rs112282669	snp	C/G	0.0150606	0.0854603	intron-variant	MYCBP2	GRCh38.p7	13:77310499	AGAACAGAGCTGCAT[C/G]GTTGCAACAGAGACT	23077
rs112295294	snp	C/T	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77178139	TTCTAAATTCACAAA[C/T]CAATGTCACTTGACA	23077
rs112299450	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77188704	CTAGAAAAGCAAATC[A/G]TTATTTGTTTCAAAA	23077
rs112315526	snp	A/G	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77224276	TCTACAAAAGCACTC[A/G]ACCATAAGATCAGAA	23077
rs112345320	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77285884	GAAAGGAAAGGAAAG[C/G]AAAGGAAAGGAAAGC	23077
rs112359634	snp	A/G	0.0146672	0.084371	intron-variant	MYCBP2	GRCh38.p7	13:77134305	GAAGCCAAGGTAGGT[A/G]GATCACTTGAGGCCA	23077
rs112364456	snp	A/C	0.5	0	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081772	GATTATGAATAACTT[A/C]CAGTTTCTCCTTTGA	23077
rs112368198	snp	C/T	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77191569	GCAGTTATATTATGC[C/T]CTAGTCTTCCTAAGC	23077
rs112373867	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77194093	ATGTTTATTCATTTA[C/T]AATAAATTTTTAATA	23077
rs112402430	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77066397	ATGTGGAGCTTAACC[A/G]GAATATAAATTCACT	23077
rs112427066	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77189255	TTTAAATCCTACCTT[C/T]GCAAGACCGAGTAGT	23077
rs112428785	snp	A/G	0.0130921	0.0798413	intron-variant	MYCBP2	GRCh38.p7	13:77169752	TTAAAACTATAGTCA[A/G]AAGGTAATTTCATTG	23077
rs112444395	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77116140	GACAGTATCTCAAAT[A/G]AGGCTGTATCAAAGT	23077
rs112493272	snp	A/G	0.00953873	0.0683987	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076515	CACAGAAATGATTAC[A/G]AATGAATGCAAAAAC	23077
rs112517967	snp	C/T	0.0700422	0.173537	intron-variant	MYCBP2	GRCh38.p7	13:77186965	TACAAGTGCGCACCA[C/T]CATACCCAGCTAATT	23077
rs112528747	snp	C/G	0.0475351	0.146656	intron-variant	MYCBP2	GRCh38.p7	13:77169252	ATACAAAAAATTAGC[C/G]GGGCGCAGTGGCGGG	23077
rs112534014	snp	C/T	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77057171	GGAGATTATTTAATG[C/T]AAGGCACTACTTAAA	23077
rs112536251	snp	A/G	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77244528	TTCAAGATGGATTAA[A/G]GATTTAAACATAAGA	23077
rs112537738	snp	A/G	0.0085026	0.0646452	intron-variant	MYCBP2	GRCh38.p7	13:77288136	AGGTTACACATCTAA[A/G]TATTAATAGAACTCA	23077
rs112546069	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77062287	ACTGATTACATTTTA[A/G]TAAAATATCTAGTCA	23077
rs112546758	snp	G/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77092026	GCAGCTTCAAAGAAA[G/T]TCTGACGAGTAATCC	23077
rs112557299	snp	A/G	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77276567	GGATGGAAGACAGAC[A/G]AAAGGCAGTACAGCA	23077
rs112588163	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77183962	AAAACCAACTTTTAG[C/T]TGTGTTAATTTTCTC	23077
rs112594731	snp	A/G	0.0134861	0.0810011	intron-variant	MYCBP2	GRCh38.p7	13:77110219	CTCCTAGCAAGGAAT[A/G]TTAAATATTAAGACC	23077
rs112604336	snp	A/G	0.5	0	synonymous-codon	MYCBP2	GRCh38.p7	13:77139306	TTGTCTCATCATTCA[A/G]CCTCAGCCACACACC	23077
rs112606389	snp	A/G	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77159226	AAAATGTATAAACTG[A/G]TCATCAAATAATCTC	23077
rs112617552	in-del	-/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77110592	CTCCCTGTTCTTGCA[-/T]CCCCTCCCTTTTTGA	23077
rs112625408	snp	C/T	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77102267	CACAATACTATATAC[C/T]ATATAGCACAGGTTG	23077
rs112643713	snp	A/G	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77070466	GCCTTAGTGTATTTT[A/G]TGTGTAGCCTAAGAC	23077
rs112676620	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77143232	AGGCATTACTTTTGC[A/G]TCTGTGAGGGTGTTT	23077
rs112695545	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77199068	AGGAACAGCTCCGGT[C/G]TACAGCTCCCAGCGT	23077
rs112698039	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77125123	GAGTCTATATGTTTC[A/G]AATTTTCTTTTAATT	23077
rs112777445	snp	C/T	0.104859	0.203554	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291054	TACCATGTTCATGGA[C/T]TGGAAAATTCAATAT	23077
rs112780359	snp	A/C	0.020175	0.0985024	intron-variant	MYCBP2	GRCh38.p7	13:77282591	TTCTTGATCCCACCC[A/C]CTCCGATCTCTCACA	23077
rs112792584	snp	C/T	0.0185938	0.0946107	intron-variant	MYCBP2	GRCh38.p7	13:77193780	ATGGTCAAACATGAC[C/T]ACTTGACGCTAATTA	23077
rs112794096	snp	A/G	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77182151	GGTCAAGAAAAATCA[A/G]GCTCCTGTCCTCTAG	23077
rs112804113	in-del	-/A	0.200182	0.244986	intron-variant	MYCBP2	GRCh38.p7	13:77214451	GTATTACATGGAGGT[-/A]AAAAAAAAAATGAAG	23077
rs112817143	snp	C/T	0.0379877	0.132479	intron-variant	MYCBP2	GRCh38.p7	13:77057443	TTCTTTTGGAGACTA[C/T]TATTATCTTGGAATC	23077
rs112840940	snp	C/T	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77256827	AGAACAGTATGGAGC[C/T]TCCCCAAAAAACTGA	23077
rs112842472	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77193640	CTTAATGAACCTTCA[C/T]AAATAAACATACTAA	23077
rs112844764	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77055009	CTCAAAAATTTTGGG[A/G]GGTCATAAACATATA	23077
rs112850991	in-del	-/A	0.5	0	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291767	GCGAAACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	23077
rs112902293	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77136067	CTTGTGATCCACCCG[C/T]CTTGGCCTCCCAAAG	23077
rs112903813	snp	A/G	0.00119518	0.0244164	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081389	ATACTAAGATCTGAA[A/G]AGAGCTAAAGAGCCG	23077
rs112907371	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77112378	ATTTATATAATATAT[A/T]ATATATATTTTATAT	23077
rs112942524	snp	C/G/T	0.0479149	0.147179	intron-variant	MYCBP2	GRCh38.p7	13:77122545	ATACAAAAAATTAGC[C/G/T]GGGCGTGGTGGCCGG	23077
rs112958058	snp	C/T	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77176343	TGGTACAACATTAGG[C/T]ACGTAGTAGGTACTC	23077
rs112996971	snp	A/C	6.72955e-05	0.00580028	intron-variant	MYCBP2	GRCh38.p7	13:77206853	AGAATAATTACAGCA[A/C]CTCAATGTGGTTTTG	23077
rs112997266	snp	A/G	0.5	0	missense	MYCBP2	GRCh38.p7	13:77181832	CAATCGGGAAGATGG[A/G]AGTCAGCTTAACAGA	23077
rs113004975	snp	A/G	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77051986	GGGAGATACAGTATG[A/G]GCATAGTGAAAGTAA	23077
rs113028996	snp	G/T	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77260705	CATTTATGACACTAT[G/T]TGTTTATTTTCACAA	23077
rs113029613	snp	A/G	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77189130	ATTATACATTTTTGA[A/G]TGGGAAAATAAATTA	23077
rs113035665	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77174188	GAATTTGTACAAGTA[A/T]GTGCTAAGAAGATAC	23077
rs113036886	snp	G/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77106740	TTTTTTTCTTTCCAA[G/T]TTTTTTCTTTCCAAC	23077
rs113045088	snp	A/G	3.29462e-05	0.00405857	intron-variant	MYCBP2	GRCh38.p7	13:77140813	AAACGTAAAAATTGA[A/G]TGATTCCGGCTCTCA	23077
rs113072502	in-del	-/AT	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77116399	CTTGGGGAGTCTTAA[-/AT]GTTGGCACTTTGCCA	23077
rs113092101	snp	A/G	0.5	0	synonymous-codon, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081888	GCTAAAACTCTCTTC[A/G]CTATCGCCATCATCT	23077
rs113102797	snp	A/G	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77303928	ATAGAGGTTATCAGG[A/G]AGCCAAAAATTGGTT	23077
rs113105732	in-del	-/TA	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77171735	TCATTTAATTTATAG[-/TA]CTTTTTAAAAGTTAA	23077
rs113139974	in-del	-/T	0.5	0	intron-variant, downstream-variant-500B	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087956	AGCTGATTTTAAAAC[-/T]TTTTTTTTTGTAGAA	23077
rs113160061	snp	A/G	0.0103295	0.0711199	intron-variant	MYCBP2	GRCh38.p7	13:77231380	GGATTACAGGCATGT[A/G]CCACCACACTGGGCT	23077
rs113163458	snp	A/G	0.00199481	0.0315187	intron-variant, nc-transcript-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087718	TACCTCCATGGATTA[A/G]GACTTCAAAGAAAGA	23077
rs113176902	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77253510	AAGAAACTGGACACA[A/G]AAGAGTTCATACTGC	23077
rs113187583	snp	C/T	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77224594	CATTTCTATCACAAC[C/T]ATACTAAAAGCAGTG	23077
rs113231711	snp	A/G	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77150468	AGTACTTTCACAGGA[A/G]CTGAAACTCAGCCTA	23077
rs113236951	snp	A/G	0.0154538	0.0865337	intron-variant	MYCBP2	GRCh38.p7	13:77266877	TGAAATGTCATATTT[A/G]CTTTAACATAGTGTC	23077
rs113244816	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77066457	AGCTGACTTTTTTCC[C/T]AGCAAGACTACAGGA	23077
rs113249335	snp	C/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77109266	AAGATGGAACTGCTC[C/G]ACCTCAGATCATCAG	23077
rs113327532	snp	C/T	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77048102	GCTGAGACTACAACA[C/T]TAACACCAATGTTAT	23077
rs113327890	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77109143	GTGGCAGGTAGAGGA[C/T]GGTTTCCTTAGTTCT	23077
rs113328217	snp	A/C	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77139750	ATTTCAAAACAAACA[A/C]CATTTTAAAATGTCA	23077
rs113363855	snp	A/C	0.0275645	0.114116	intron-variant	MYCBP2	GRCh38.p7	13:77170721	AGCTAGGATTACAGG[A/C]ACCTGCCACCACGCC	23077
rs113374698	snp	A/G	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77289324	ATCCAGAGATATTAC[A/G]AGTATTAGCTATTCA	23077
rs113376179	snp	A/C	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77257539	ATAAAATTTTTAAAA[A/C]AAATTTAAATAGGAA	23077
rs113379493	snp	C/T	0.0130921	0.0798413	intron-variant	MYCBP2	GRCh38.p7	13:77167732	TGCTTTAAAACAATA[C/T]AGGAGGTTAGGAAGT	23077
rs113381176	snp	C/T	0.0869089	0.189476	intron-variant	MYCBP2	GRCh38.p7	13:77134284	TCTGTAATCCCAGCA[C/T]TGTGGGAAGCCAAGG	23077
rs113393090	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77182330	TGCAAATTATAAATC[A/T]GTGCTATTACAAGCA	23077
rs113414890	snp	C/G	0.00199481	0.0315187	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076059	TGACTTCTCTTTTTG[C/G]AAATGGATGAAGTAC	23077
rs113416352	in-del	-/CAGT	0.00203019	0.0317958	intron-variant	MYCBP2	GRCh38.p7	13:77065972	ACTTCACTGCCAAAA[-/CAGT]CAGAAGAATGGGAAC	23077
rs113443182	snp	C/G	0.0130921	0.0798413	intron-variant	MYCBP2	GRCh38.p7	13:77178146	TTCACAAATCAATGT[C/G]ACTTGACAGTATTTT	23077
rs113443880	snp	A/G	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77212229	TTCATAAAGTTAAGG[A/G]GGCAGTAGATAAAAA	23077
rs113444459	snp	A/G	0.5	0	synonymous-codon	MYCBP2	GRCh38.p7	13:77176518	AGGAACCACTTTGTC[A/G]AGTCTGATCTCAGCT	23077
rs113447343	snp	A/G/T	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77249129	AGGGAAGAATGAGGA[A/G/T]TCATTGTTTAACAGT	23077
rs113452218	snp	C/T	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77145966	GTATTATGTAATATA[C/T]TGGCAGTATTACAGT	23077
rs113506252	snp	C/T	0.00993419	0.0697739	intron-variant	MYCBP2	GRCh38.p7	13:77310329	CCTGAATTCACAATG[C/T]AGCTCCAGCAACGAT	23077
rs113526687	snp	G/T	0.00953873	0.0683987	intron-variant	MYCBP2	GRCh38.p7	13:77269824	TTGAACCTCTTATGA[G/T]TTCTGAGACAGTGTT	23077
rs113546442	snp	A/C	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77091899	AATCACACTTGTCAG[A/C]CTAGCCTCAAAACAG	23077
rs113547395	snp	A/G	0.0197687	0.0974348	intron-variant	MYCBP2	GRCh38.p7	13:77066876	TGACTACTGGCATTT[A/G]TAAGTTTTTTTCTGT	23077
rs113602515	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77131614	GGAAAATGTTAATTT[C/T]TCCAAAGCCCCAATT	23077
rs113602798	snp	A/C	0.5	0	missense	MYCBP2	GRCh38.p7	13:77190276	AACTGAGGTATCTGA[A/C]CCGCATTAACATCTG	23077
rs113604514	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77225655	AAGAGAAAAATGTTA[A/C]AAGGAACAAGCAAGA	23077
rs113622838	snp	C/G	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77051416	GATTTAATAAGCAAG[C/G]TACTTAATTTCTTTA	23077
rs113624086	in-del	-/C	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77126657	TCAATATAAAAAAAA[-/C]ACATAACTAAAGATA	23077
rs113625592	in-del	-/T	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77054604	GAGATTGGTAAAGTC[-/T]TTTTTTTTTTTTTTG	23077
rs113626238	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77135635	TAGAGCCCTATGCCA[A/G]TTAATTTTGCCATAC	23077
rs113626968	snp	A/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77106728	CTTTAAGTTCCTTTT[A/T]TTTCTTTCCAATTTT	23077
rs113668644	snp	A/T	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77172074	CCCAGCTAATTTTTC[A/T]GTTTTTAGTAGAGAT	23077
rs113670389	snp	C/T	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77296505	TTCAGCACATACTAA[C/T]AAAATGGTTTAATTA	23077
rs113675544	snp	C/T	0.0103295	0.0711199	intron-variant	MYCBP2	GRCh38.p7	13:77253138	ATATAAAACATAATA[C/T]GTAAAAAAGCTCCTA	23077
rs113698672	snp	A/G	0.5	0	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77079461	ATATCTTAAGGCTGA[A/G]TAAGTTTTACGCAAA	23077
rs113704459	snp	C/T	0.00128154	0.025281	intron-variant	MYCBP2	GRCh38.p7	13:77055521	CATATAGGTAAGCTC[C/T]AGTTTTTAAAACTTC	23077
rs113751699	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77110180	AAACAGATGTGCAAG[C/T]AGGAGAGATATCACT	23077
rs113751873	snp	C/T	0.5	0	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77078599	GTAGGTACAATATAA[C/T]TGCTCATGACTGGGG	23077
rs113755658	snp	A/C	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77148379	CAGCCACTCACACCA[A/C]AAGTCACAGACCTGT	23077
rs113756311	snp	A/G	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77263578	TGAACTGGTGAAAAC[A/G]CAATGTTCATTTTTA	23077
rs113777599	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77155913	ACTAATTAATATAAA[C/T]AAGTCATTTAAACAA	23077
rs113779220	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77118797	GAACGAAGACTCTAT[A/G]AAGAATCAGTGATAA	23077
rs113789794	in-del	-/A	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77243621	CCATCTCAAAAAAAG[-/A]AAAAAAAAAAAAAGA	23077
rs113829824	snp	C/T	0.5	0	missense	MYCBP2	GRCh38.p7	13:77267906	ATGGCTGTCATGCTG[C/T]GGTTATTCACATCTC	23077
rs113832891	snp	A/G	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77134716	AAAATTATTTTGGAA[A/G]CGATACAGTCATAAT	23077
rs113842102	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77050226	ATTAAGCTGTTTTCC[A/G]GAGAGGTCTATCACT	23077
rs113847001	snp	A/C	0.0185938	0.0946107	intron-variant	MYCBP2	GRCh38.p7	13:77265372	GGGTGAGGAGTGAAG[A/C]GGCGCAAGAAGAGTA	23077
rs113858070	snp	A/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77062420	CCATATACTATGAAG[A/T]AGGGACTCTCTGAAA	23077
rs113859446	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77047670	CTAAAGACATGCCCA[C/T]GGCTGCACAGACAGA	23077
rs113902194	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77161576	CCTTTCTCTAGCAGG[C/T]AAAAAAAGAAAAACA	23077
rs113903211	snp	A/G	0.5	0	synonymous-codon	MYCBP2	GRCh38.p7	13:77185962	TAAATCTAGGAGTGT[A/G]GCTGTGAACTGGAAT	23077
rs113905622	snp	A/G	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77225231	ACAGACTAGAAGTTA[A/G]ATCTCTAGACAAGTA	23077
rs113913927	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77253070	ATTTTGACATCAAAA[C/T]TTTAAAATTATACAT	23077
rs113967371	snp	A/C/G	0.00321455	0.0399622	intron-variant	MYCBP2	GRCh38.p7	13:77205409	TAAATCATAATCTAT[A/C/G]TTTTAAAAGATCCAT	23077
rs113986547	snp	A/G	0.5	0	intron-variant	MYCBP2	GRCh38.p7	13:77241919	ATCATGCCATTTCTA[A/G]TAAGCATTTAAAATA	23077
rs114006768	snp	A/G	0.00243654	0.0348186	intron-variant	MYCBP2	GRCh38.p7	13:77093161	CAGGAGAGAACTAAA[A/G]TACCTTGGTGGCATA	23077
rs114020406	snp	A/G	0.0170251	0.090679	intron-variant	MYCBP2	GRCh38.p7	13:77180750	TAAGACTTTGTCTCT[A/G]CAAAATGTTTTTTTA	23077
rs114058195	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77184903	CAACTGCACAATGTG[C/G]CTACCAATTTTGTAA	23077
rs114127060	snp	A/G	0.0513262	0.151752	intron-variant	MYCBP2	GRCh38.p7	13:77240130	TTGTTTTTAAATAAA[A/G]ATTGCTTAATGGAGT	23077
rs114128676	snp	A/C	0.0271762	0.113356	intron-variant	MYCBP2	GRCh38.p7	13:77090622	CACCAAATAGAAAGA[A/C]AATGGATATGTACAC	23077
rs114244488	snp	C/T	0.0256215	0.110247	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291977	CAGAGCAATGGACCA[C/T]GCCTCCTGGCCTGTC	23077
rs114246108	snp	C/T	0.00557542	0.0525036	intron-variant	MYCBP2	GRCh38.p7	13:77045724	GGGTCCCTTACTCAC[C/T]ATATCCTGCCTAGAG	23077
rs114249415	snp	A/C	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77261747	GTGACACAGAGACAC[A/C]AAGTGAGCACAGGCG	23077
rs114386672	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77219163	TTTTAGATACAGACC[A/G]AGGAAGAACAGCTCA	23077
rs114386691	snp	A/G	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77299736	TATTCTAAATCAATC[A/G]AAGCTTAATGAAGAA	23077
rs114389879	snp	A/T	0.0236746	0.106192	intron-variant	MYCBP2	GRCh38.p7	13:77125127	CTATATGTTTCGAAT[A/T]TTCTTTTAATTTTCT	23077
rs114449292	snp	C/T	0.0107246	0.0724382	intron-variant	MYCBP2	GRCh38.p7	13:77142629	GTCCCACGATAAGGA[C/T]TAAACATAGTCAGAC	23077
rs114449341	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77196864	ATTTAAAAGTCATCA[A/G]AGATAAATGTCCATG	23077
rs114480593	snp	A/G	0.00478085	0.0486577	intron-variant	MYCBP2	GRCh38.p7	13:77062325	AGACTCTGGCTAAAA[A/G]TAAATTTTGATATGA	23077
rs114511789	snp	G/T	0.0341408	0.126114	intron-variant	MYCBP2	GRCh38.p7	13:77154457	GGTTAAAAAAAGAAC[G/T]CTAAGATGAAAAGAA	23077
rs114564224	snp	C/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77209620	TGGTTCTTAATACCT[C/G]ATGTCTTCATAAGAA	23077
rs114568195	snp	C/T	0.0146672	0.084371	intron-variant	MYCBP2	GRCh38.p7	13:77129104	ACACAAAATTTGTTA[C/T]ACATGCTGAAATACC	23077
rs114568287	snp	A/G	0.0256215	0.110247	intron-variant	MYCBP2	GRCh38.p7	13:77279992	GAACATGTCTTAAAC[A/G]GCTTAATACCTCCCA	23077
rs114573489	snp	A/C	0.0263992	0.111815	intron-variant	MYCBP2	GRCh38.p7	13:77125766	TTTTCTTTTTTCTGC[A/C]TCTAAAATGTCCTAA	23077
rs114584873	snp	C/T	0.00381769	0.0435232	intron-variant	MYCBP2	GRCh38.p7	13:77150689	TGTTGGTTAAATAAA[C/T]AAATGCTGAAAACTA	23077
rs114670016	snp	A/G	0.0263992	0.111815	intron-variant	MYCBP2	GRCh38.p7	13:77264403	GTCACAGAAAAATAC[A/G]ACCTAAAGCTTCTGT	23077
rs114686299	snp	C/T	0.0240643	0.107019	intron-variant	MYCBP2	GRCh38.p7	13:77258945	AGATTAAGTAAACTG[C/T]TACCCAATTAAAAGC	23077
rs114689017	snp	A/G	0.0228947	0.104514	intron-variant	MYCBP2	GRCh38.p7	13:77149069	CAAATATGTAACTCT[A/G]TCTCTATTAATAAGA	23077
rs114748609	snp	C/T	0.0182019	0.0936463	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076421	CGTAAAAAAGTTTCA[C/T]GAAGAAGACAGTACT	23077
rs114759769	snp	C/T	0.0341408	0.126114	intron-variant	MYCBP2	GRCh38.p7	13:77309711	CTGCAACTGTCTCTT[C/T]AAAGGTAGCCCTGCT	23077
rs114809603	snp	C/T	0.0279526	0.114869	intron-variant	MYCBP2	GRCh38.p7	13:77267323	GAAGCATAAGAAGCA[C/T]AAATGATGAAATTAA	23077
rs114812291	snp	C/T	0.0341408	0.126114	intron-variant	MYCBP2	GRCh38.p7	13:77300162	AAGATTTTAATAAAT[C/T]CAAATTTACAGAACT	23077
rs114816028	snp	C/T	0.00914312	0.0669923	intron-variant	MYCBP2	GRCh38.p7	13:77133156	CGGAACATAAATGCA[C/T]GGGCTTTGGAATCAT	23077
rs114843277	snp	C/T	0.0232847	0.105357	intron-variant	MYCBP2	GRCh38.p7	13:77303717	GTAGAATGCTGCTAA[C/T]GCAGTACTTCCACAA	23077
rs114879521	snp	C/T	0.0256215	0.110247	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77292136	TGAGCAAAAACAATA[C/T]ACACATTTCTCTGTA	23077
rs114891592	snp	A/C	0.0329836	0.124112	intron-variant	MYCBP2	GRCh38.p7	13:77270149	GGTGAATGACATTTA[A/C]TGCATGTATTTCAAT	23077
rs114984826	snp	A/G	0.0240643	0.107019	intron-variant	MYCBP2	GRCh38.p7	13:77211871	AAAAGCTACAAAAGT[A/G]CATTTCATTAAAGGG	23077
rs115011557	snp	A/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77279998	GTCTTAAACGGCTTA[A/T]TACCTCCCATGCCTA	23077
rs115016158	snp	A/G	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77108534	AGTTGCAAGGGAAAA[A/G]TATTAATTATACATC	23077
rs115076298	snp	C/T	0.0256215	0.110247	intron-variant	MYCBP2	GRCh38.p7	13:77307378	GGAAAAAAGTTTAAG[C/T]AATCCTCTATCCCTC	23077
rs115083196	snp	A/G	0.0228947	0.104514	intron-variant	MYCBP2	GRCh38.p7	13:77146582	GCATCCATAACATAT[A/G]GAGAATAAATCCATA	23077
rs115091489	snp	C/T	0.00953873	0.0683987	intron-variant	MYCBP2	GRCh38.p7	13:77128416	ATAATATTCCTAGTG[C/T]ATTTAATTAATTATA	23077
rs115092351	snp	A/G	0.00796617	0.0626069	intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326451	CGGCATGGGGCGCAA[A/G]GAAGGGCACCCTGGG	23077
rs115189680	snp	C/G	0.0263992	0.111815	intron-variant	MYCBP2	GRCh38.p7	13:77320734	CACAACCTCTGGATG[C/G]GATGCAACATGCAGT	23077
rs115202165	snp	C/T	0.0236746	0.106192	intron-variant	MYCBP2	GRCh38.p7	13:77136059	CTGCTAACCTTGTGA[C/T]CCACCCGTCTTGGCC	23077
rs115205067	snp	A/C	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77105189	CATAGCAGGAAGACA[A/C]AGGAATAGGAAATCA	23077
rs115217924	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77148219	ACAAATATTTATTTC[A/G]GATATAGAATTCATA	23077
rs115276949	snp	C/T	0.0314385	0.121371	intron-variant	MYCBP2	GRCh38.p7	13:77116452	TATAAAAAATACAAT[C/T]CTGAATTATTTTAAA	23077
rs115295480	snp	C/G	0.0185938	0.0946107	intron-variant	MYCBP2	GRCh38.p7	13:77155546	TAATATTTCAGGTAA[C/G]AGGTATCCTAAAAAC	23077
rs115299440	snp	A/G	0.0379877	0.132479	intron-variant	MYCBP2	GRCh38.p7	13:77277043	GTTCTAGTTTTAAAA[A/G]AATAAAGGAAAGAAA	23077
rs115364558	snp	A/G	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77054087	GGAGGTGAAACCTGA[A/G]CTGAAGCCCGAGGTA	23077
rs115438215	snp	A/G/T	0.00953873	0.0683987	intron-variant	MYCBP2	GRCh38.p7	13:77253021	CTCTCACCAGGCTAC[A/G/T]TTCATCAAAAATTTA	23077
rs115481459	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77101405	AATACCTGCTGATGC[C/T]ACCTCTATTCTAGGA	23077
rs115506448	snp	A/G	0.0174175	0.0916809	intron-variant	MYCBP2	GRCh38.p7	13:77315617	AACTATCAGCAAGCC[A/G]GGTGCGATGGCTCAC	23077
rs115633540	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77161820	TAATGAATGAACCCA[A/G]TGGTCAAGACAAATA	23077
rs115683128	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77113687	TAGGATGAAGTAAAG[C/G]GTGGATGAATAAATC	23077
rs115690425	snp	C/T	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77180491	CTTAGAAGTTCTTTT[C/T]TGAATTATCTGTCTC	23077
rs115726915	snp	A/G	0.0189856	0.0955633	intron-variant	MYCBP2	GRCh38.p7	13:77264176	CTAATTCAACTAATC[A/G]TACTTATTACATTTT	23077
rs115732189	snp	A/G	0.00557542	0.0525036	intron-variant	MYCBP2	GRCh38.p7	13:77104593	TGACCAAATAGATGA[A/G]GATGTAGAAAGGAGA	23077
rs115735839	snp	C/T	0.0325976	0.123435	intron-variant	MYCBP2	GRCh38.p7	13:77296153	GGCTGGGCACAGTGG[C/T]TCATGTCTGCAATGT	23077
rs115747082	snp	C/G	0.0260105	0.111035	intron-variant	MYCBP2	GRCh38.p7	13:77113222	AAGTCCTTCAACACT[C/G]TGAGTAGGACCTGCC	23077
rs115788844	snp	A/T	0.0256215	0.110247	intron-variant	MYCBP2	GRCh38.p7	13:77231078	AAAATAGGGTACCAA[A/T]TGATAAATTATTATT	23077
rs115838033	snp	A/T	0.0146672	0.084371	intron-variant	MYCBP2	GRCh38.p7	13:77250820	CAACAGAAAGAAATA[A/T]AATAGATATCTAGCA	23077
rs115859076	snp	A/G	0.0263992	0.111815	intron-variant	MYCBP2	GRCh38.p7	13:77130692	TACTGGTTCATCCAC[A/G]TATATAAGAATTTGT	23077
rs115861532	snp	G/T	0.0244538	0.107838	intron-variant	MYCBP2	GRCh38.p7	13:77124545	ATTACAAAACTTCAT[G/T]AGCAACTAGTATGTG	23077
rs115900693	snp	C/G/T	0.00438332	0.0466095	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77327310	GCTGTCAGCTACTGA[C/G/T]GTTCGACTTCAGGTT	23077
rs115900776	snp	A/G/T	0.0193847	0.0965802	intron-variant	MYCBP2	GRCh38.p7	13:77287940	GATCTCCCTTCCTGC[A/G/T]CTTTCCAGTGAATTA	23077
rs115910637	snp	C/T	0.00953873	0.0683987	intron-variant	MYCBP2	GRCh38.p7	13:77130306	TTAGATAATGAAACT[C/T]TTCTCATTATCTCAT	23077
rs115917452	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77082592	TTTCAAATTGAAATT[A/G]GAATCTGTTGAGCAT	23077
rs115930817	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77297030	AAGAAAAAAAATCTG[C/T]TCTTTTTGGTAGTGA	23077
rs115952728	snp	C/T	0.0263992	0.111815	intron-variant	MYCBP2	GRCh38.p7	13:77160272	CAAACTGCCAGCGAA[C/T]AAATCCCAGTGCAGT	23077
rs115957793	snp	A/G	0.0107246	0.0724382	intron-variant	MYCBP2	GRCh38.p7	13:77185642	AATTAAACTTTATTA[A/G]ATTATTTAACTTTGG	23077
rs116070827	snp	A/T	0.0337553	0.125452	intron-variant	MYCBP2	GRCh38.p7	13:77219009	TGATCGATATGGGGC[A/T]AGGAAGATTTTTTTT	23077
rs116079114	snp	A/G	0.0267878	0.112589	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77227559	AATAAGACGCCAGAT[A/G]TAAAGAAATTTTACG	23077
rs116137655	snp	A/G	0.00478085	0.0486577	intron-variant	MYCBP2	GRCh38.p7	13:77055254	GGAATGGTTAGCAGA[A/G]TCAAGTGAGAGAAGT	23077
rs116158808	snp	C/T	0.0341408	0.126114	intron-variant	MYCBP2	GRCh38.p7	13:77154322	GTCAAGGAAAGATAG[C/T]AGGAGAAGCAAATAT	23077
rs116184451	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77256252	TATACGCCAGAAAGA[C/T]TGCTGCCAAAAATGG	23077
rs116235181	snp	C/T	0.00557542	0.0525036	intron-variant	MYCBP2	GRCh38.p7	13:77307181	TTCCTCCTTCCCCCA[C/T]CCCAAAAGAGACAGC	23077
rs116242207	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77242626	ACTATGTCCAAATGA[C/T]AATGAGCATAAATGA	23077
rs116268248	snp	A/G	0.0138799	0.0821421	intron-variant	MYCBP2	GRCh38.p7	13:77268131	CATTATTGAAAATTG[A/G]TGTAACATATTCCCA	23077
rs116301370	snp	C/T	0.0228947	0.104514	intron-variant	MYCBP2	GRCh38.p7	13:77222628	CATCCTATCAAGGAC[C/T]ACTCCCCACCCCTGT	23077
rs116323716	snp	A/G	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77255854	ACAGCATTAATCCTC[A/G]AAATTATTGGTACTT	23077
rs116325290	snp	C/T	0.0111196	0.0737302	intron-variant	MYCBP2	GRCh38.p7	13:77247170	AAGAAGTAAAATTAT[C/T]TATGTTCACAGATAA	23077
rs116394466	snp	C/T	0.0513262	0.151752	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075490	TTCTCTCTACTAATC[C/T]CATTTGAATCCCTTC	23077
rs116408676	snp	C/T	0.00993419	0.0697739	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77327869	TTGTGACGGAGACTG[C/T]ATAGCGTCTGAAAAT	23077
rs116444143	snp	A/G	0.0256215	0.110247	intron-variant	MYCBP2	GRCh38.p7	13:77276770	CTCCTGGGCTCGAGC[A/G]GTCCTCCCACCTTAG	23077
rs116450257	snp	C/T	0.0142736	0.0832652	intron-variant	MYCBP2	GRCh38.p7	13:77130089	TTCGTAGTTATCTCA[C/T]GCTATCAATCTATAT	23077
rs116498760	snp	C/T	0.0256215	0.110247	intron-variant	MYCBP2	GRCh38.p7	13:77263423	GCAAAAAAGAGAAAT[C/T]ATTAGTCAATTCCTT	23077
rs116525466	snp	C/T	0.0275645	0.114116	intron-variant	MYCBP2	GRCh38.p7	13:77282940	CTGTCACTACCATAA[C/T]TCCAACCCTCATTAA	23077
rs116529824	snp	A/C/G	0.243465	0.272379	intron-variant	MYCBP2	GRCh38.p7	13:77063582	AAAAAAAAAAAAAAA[A/C/G]ACAACTGTTTTCAGA	23077
rs116551378	snp	A/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77314200	ACTAGATTTAACCAT[A/T]CCCCAATGTATATGT	23077
rs116560337	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77246672	AGGGGCAGGGGGAGG[A/C]AAAAAAAAAAACCCC	23077
rs116561007	snp	A/G	0.0414363	0.137845	intron-variant	MYCBP2	GRCh38.p7	13:77159732	GATTGTAAGTTTCCT[A/G]AGGCCTCCTCAGCCA	23077
rs116585793	snp	C/T	0.0244538	0.107838	intron-variant	MYCBP2	GRCh38.p7	13:77047880	ATTCCTTCCCCTTTC[C/T]AGTCCATAAAAACCC	23077
rs116613331	snp	C/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77135546	CATACCTGTCCCTGC[C/T]TATGCCAGGCCTCTG	23077
rs116615614	snp	C/T	0.0240643	0.107019	intron-variant	MYCBP2	GRCh38.p7	13:77230252	CTCCTTACACCCTCA[C/T]AAAAAAGTCACAGTC	23077
rs116648901	snp	C/T	0.00638801	0.0561534	intron-variant	MYCBP2	GRCh38.p7	13:77168401	GCCAAGTTTTACATT[C/T]GAATCACACTAAGAA	23077
rs116673060	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77196629	TAGAATCAAGGATGA[C/T]TCCAAGATTTTTGGC	23077
rs116701306	snp	C/T	0.0107246	0.0724382	intron-variant	MYCBP2	GRCh38.p7	13:77234508	AATTATGTTTCTAGA[C/T]ATAAACAAAAATGCA	23077
rs116729876	snp	C/T	0.00557542	0.0525036	intron-variant	MYCBP2	GRCh38.p7	13:77108422	AATAACTTCAAAATA[C/T]AAGAGACAGGTATTG	23077
rs116734648	snp	C/T	0.0287284	0.116357	intron-variant	MYCBP2	GRCh38.p7	13:77172507	GCTGTAGAGAACTGA[C/T]TGTAGGAGACCAATA	23077
rs116766455	snp	A/C	0.00557542	0.0525036	intron-variant	MYCBP2	GRCh38.p7	13:77254554	GAGTTTTCATACATG[A/C]ATATAATGTCTAATG	23077
rs116793057	snp	C/G	0.00478085	0.0486577	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77073865	ACAAAACACTGCTGA[C/G]AGAAATTTTAAACAG	23077
rs116813747	snp	C/T	0.0146672	0.084371	intron-variant	MYCBP2	GRCh38.p7	13:77176823	TTCTTGAGAAGACTA[C/T]AACATAAATAAGCTT	23077
rs116815446	snp	A/G	0.0263992	0.111815	intron-variant	MYCBP2	GRCh38.p7	13:77111634	TCGCTTTGTTGTCCA[A/G]ACTGGTCCTAAGCAT	23077
rs116845341	snp	A/C	0.04875	0.148319	intron-variant	MYCBP2	GRCh38.p7	13:77274398	TCCATAGAACGGAGA[A/C]TTGAAAATCCTTATA	23077
rs116847421	snp	C/T	0.108755	0.206276	intron-variant	MYCBP2	GRCh38.p7	13:77049790	ACAGGTACCCGCCAC[C/T]ATGCCTGGCTAATTT	23077
rs116875836	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77276030	CTACTTTCCTCCATA[C/T]GATTTATCCACATTT	23077
rs116927180	snp	A/C	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77161403	GCAAACAATAATAAA[A/C]ACAACAAATGATGGC	23077
rs116930853	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77276394	AGATTAAAAAAAGGA[A/G]GAGAGGCAAGTTTCA	23077
rs116934611	snp	C/T	0.00755907	0.0610114	intron-variant	MYCBP2	GRCh38.p7	13:77155362	GCTCTAAGCTTCAAA[C/T]AACCAATCACTCTAT	23077
rs116943441	snp	A/C	0.0193772	0.0965046	intron-variant	MYCBP2	GRCh38.p7	13:77063765	AAAATAGGGACAGAA[A/C]AATAGAAAAAGAAAT	23077
rs116957494	snp	A/G	0.00229008	0.0337609	missense	MYCBP2	GRCh38.p7	13:77098791	TTATGGTTGGGGGAT[A/G]ATGACCTACTGTGGG	23077
rs116990622	snp	C/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77090704	GGTGTCTTCAGTGTT[C/G]TGTGAGGTTTCTCAC	23077
rs117026543	snp	A/G	0.00279162	0.0372561	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77083505	AGTGTGTGTGCATAT[A/G]TATGTATGTGTATGG	23077
rs117060749	snp	C/T	0.00333536	0.0407008	intron-variant	MYCBP2	GRCh38.p7	13:77194293	ATCAGCTATACATAT[C/T]TGATGAACAATGTGT	23077
rs117061469	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77182241	CAAAGGGAGATGCCA[A/G]AAAGGCCCCAATTAG	23077
rs117062806	snp	C/G	0.0614824	0.164198	intron-variant	MYCBP2	GRCh38.p7	13:77137887	CCTCGCCTGGCTCTC[C/G]CATCTGTATAAAAAA	23077
rs117092082	snp	A/G	0.00478085	0.0486577	intron-variant	MYCBP2	GRCh38.p7	13:77096930	TACAGAAATCATTAC[A/G]TTTACTGAAAATGCA	23077
rs117094441	snp	C/T	0.00835141	0.0640778	intron-variant	MYCBP2	GRCh38.p7	13:77109075	CTCAAAATGGGAATA[C/T]GTGTTAATTAGGGAA	23077
rs117193528	snp	G/T	0.0228947	0.104514	intron-variant	MYCBP2	GRCh38.p7	13:77300532	AAAAACAAGAATTGG[G/T]CCTCATTGGTCTGTG	23077
rs117200503	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77051651	ATCGCCCAAAGGAAA[C/T]AATATATATGAAATA	23077
rs117251882	snp	A/T	0.00716266	0.059414	intron-variant	MYCBP2	GRCh38.p7	13:77312333	AACACAAAATACTAG[A/T]TTTTTCCTCTAAGTT	23077
rs117264754	snp	A/G	0.126219	0.217206	intron-variant	MYCBP2	GRCh38.p7	13:77089625	GGGGCTGTTGATACC[A/G]ACTGGTCCAGATCAT	23077
rs117338692	snp	C/T	0.00953873	0.0683987	intron-variant	MYCBP2	GRCh38.p7	13:77093847	GAAAAATATTAGATA[C/T]ATGAAATTTTCTGTG	23077
rs117360108	snp	A/T	0.0327778	0.123752	intron-variant	MYCBP2	GRCh38.p7	13:77310534	GGCCCATAAAGTCTA[A/T]GTTATTTACTATCTG	23077
rs117392941	snp	C/T	0.0165278	0.0893908	intron-variant	MYCBP2	GRCh38.p7	13:77175532	TCTTCCTGATGAAAC[C/T]TCTCGTGTACCGATC	23077
rs117406235	snp	C/T	0.0217236	0.101931	intron-variant	MYCBP2	GRCh38.p7	13:77091045	TCACCTGAATTCAAA[C/T]TGGAATATTTTTGCT	23077
rs117419823	snp	C/T	0.0174175	0.0916809	intron-variant	MYCBP2	GRCh38.p7	13:77247039	CTGAAAGCTTTTCCT[C/T]GTAATATCAGGAAGA	23077
rs117425231	snp	C/T	0.00597247	0.0543191	utr-variant-3-prime	MYCBP2	GRCh38.p7	13:77045048	CTTGAAAGCCAGCAT[C/T]GTTCTTAGTCCATGG	23077
rs117470816	snp	C/T	0.0644693	0.167566	intron-variant	MYCBP2	GRCh38.p7	13:77186790	GCTCCTGAAAACGAG[C/T]TTATAGATTCAATTT	23077
rs117483909	snp	C/T	0.0130921	0.0798413	intron-variant	MYCBP2	GRCh38.p7	13:77214683	ATCAGAGTGGACTTA[C/T]ACAAACCTAGACGGT	23077
rs117520191	snp	G/T	0.0228947	0.104514	intron-variant	MYCBP2	GRCh38.p7	13:77127478	CATTGTCATCATTAC[G/T]CCTTTAAAAGAGATT	23077
rs117535899	snp	A/G	0.0547245	0.156101	intron-variant	MYCBP2	GRCh38.p7	13:77275706	AAAGGAATCTTGGCC[A/G]GGCGCAGTGGCTCAT	23077
rs117549404	snp	A/G	0.00557542	0.0525036	intron-variant	MYCBP2	GRCh38.p7	13:77271959	CCATGTTAAGGTAAT[A/G]GGCTTTAATATGGAG	23077
rs117551055	snp	A/G	0.00914312	0.0669923	intron-variant	MYCBP2	GRCh38.p7	13:77144205	CACCTGACTAGTAAC[A/G]TCAGGAAATGGAGGG	23077
rs117562874	snp	A/T	0.0618563	0.164627	intron-variant	MYCBP2	GRCh38.p7	13:77130998	GATATTTTAAAATGA[A/T]GTTAACTGCTAACTG	23077
rs117639927	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77254141	GTAGAAAAATGTAAA[C/T]AACAGATTAACACTT	23077
rs117641427	snp	C/T	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77094905	CCGAGTATGAGTACA[C/T]AGAAGCCAGGATTTT	23077
rs117669442	snp	C/T	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77320808	GAACACCTAATAAAC[C/T]CTTAAGGTCTAGCTT	23077
rs117682347	snp	A/T	0.0267878	0.112589	intron-variant	MYCBP2	GRCh38.p7	13:77218862	AAATGTAATTATGAC[A/T]CTTTAAATTTTAAAA	23077
rs117722214	snp	A/T	0.102766	0.202045	synonymous-codon, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326713	GGCGGCTGGGTAGAA[A/T]CCGTCCCCGCCGAGC	23077
rs117725397	snp	C/T	0.0217236	0.101931	intron-variant	MYCBP2	GRCh38.p7	13:77257104	GATGTAACTGGAGGA[C/T]ATTATGTTAAGTGAA	23077
rs117727264	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77170918	GCTGCCAGTGTGAAG[A/T]ATAACTAAACAACTA	23077
rs117730227	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77319300	AGTAGAAGAAGGCCA[C/T]TTCTGCAGGCCCAGA	23077
rs117804568	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77304043	GGGAATGTGAATTAG[G/T]ACAACCATTGTGGAA	23077
rs117823495	snp	A/G	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77147419	GAAACTTGGCACATT[A/G]TTCTGAATACTTCTG	23077
rs117836900	snp	C/T	0.0162599	0.0886879	synonymous-codon	MYCBP2	GRCh38.p7	13:77051811	AAATGTTCTGCCTAC[C/T]TGAGCCCTGGAAACA	23077
rs117842808	snp	C/T	0.0257374	0.110482	intron-variant	MYCBP2	GRCh38.p7	13:77174298	TTTCCGTTATCTCTA[C/T]ACATTCACCCACCTA	23077
rs117884376	snp	G/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77317638	CAAATGATTCTCCTA[G/T]TCTATAAAAGTGGGT	23077
rs117885044	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77093433	AGCACATGTAAATCA[C/T]AGTTAAAGGCAAAGC	23077
rs117908295	snp	A/G	0.00049412	0.0157104	synonymous-codon	MYCBP2	GRCh38.p7	13:77174358	GGTTTGGTTTGTGCC[A/G]TTACTGCTCAAGCTG	23077
rs117935000	snp	C/G	0.00676609	0.0577691	intron-variant	MYCBP2	GRCh38.p7	13:77172999	AGGTGAAATAACACA[C/G]GTAACATACTCAAAG	23077
rs117936226	snp	A/C	0.0383715	0.133092	intron-variant	MYCBP2	GRCh38.p7	13:77220414	AAGATCATATAGCTA[A/C]CAAGTGACAGAATCA	23077
rs117937242	snp	A/C	0.00478085	0.0486577	intron-variant, utr-variant-5-prime, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77292349	TGAGTCCTTCTGGCA[A/C]ATCAAAGGAAAAACC	23077
rs117940352	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77053652	TATAATGTTTAGTAC[A/G]TGAAACACACAGAAA	23077
rs117967756	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77107010	TGCTATACATACCTA[C/T]GTTTATGTATTTATA	23077
rs117974296	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77304342	CACCGTGGATGAGCC[G/T]GGAGGACATTATCTT	23077
rs118007583	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77307083	TAAGATCTAGAAAAC[A/G]GATCAGAAAAAGAAT	23077
rs118011687	snp	C/T	0.00993419	0.0697739	intron-variant	MYCBP2	GRCh38.p7	13:77141449	CAGTATCTAACTCAC[C/T]GAGCTGTTGTAGGAA	23077
rs118013936	snp	G/T	0.0360663	0.129354	intron-variant	MYCBP2	GRCh38.p7	13:77255671	TTCTTTTGTTCCTTC[G/T]TCATTTGCCAATATA	23077
rs118014192	snp	A/G	0.0414363	0.137845	intron-variant	MYCBP2	GRCh38.p7	13:77110402	AATTGAGGTCAGATC[A/G]GTTCTCTGCTCTTGA	23077
rs118024837	snp	A/G	0.00993419	0.0697739	intron-variant	MYCBP2	GRCh38.p7	13:77195406	GTTTGACACCAGCCT[A/G]GTCAACATGGTGAAA	23077
rs118051938	snp	A/C	0.00597247	0.0543191	intron-variant	MYCBP2	GRCh38.p7	13:77221626	TGACTGAGACCCCAT[A/C]TTATCTAACTGCAAT	23077
rs118092420	snp	A/G	0.0166325	0.0896639	intron-variant	MYCBP2	GRCh38.p7	13:77096919	TTAGTCAATGTTACA[A/G]AAATCATTACATTTA	23077
rs118094074	snp	A/C	0.00478085	0.0486577	intron-variant	MYCBP2	GRCh38.p7	13:77151921	AATACCACTTTAGTT[A/C]TTCAGCAGGTATCAC	23077
rs118104584	snp	A/C	0.0119091	0.0762411	intron-variant	MYCBP2	GRCh38.p7	13:77217081	TAACCAGATATTCTA[A/C]ACACTGTTCTTAGTT	23077
rs118115161	snp	C/T	0.00636936	0.0560724	intron-variant	MYCBP2	GRCh38.p7	13:77279991	GGAACATGTCTTAAA[C/T]GGCTTAATACCTCCC	23077
rs137865219	snp	A/C	0.00755907	0.0610114	intron-variant	MYCBP2	GRCh38.p7	13:77050925	TCACTTGAAACAGAG[A/C]TTTCATATAATGTTT	23077
rs137885458	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77048008	CTTTGTATCTGTGCT[C/T]CTTAATCTTCTTGGA	23077
rs137887130	snp	A/G	0.0252325	0.109451	intron-variant	MYCBP2	GRCh38.p7	13:77136786	CAACCTCTTCCCTTC[A/G]TCCCTCCCTCCTCTA	23077
rs137914116	snp	C/T	0.00597247	0.0543191	intron-variant	MYCBP2	GRCh38.p7	13:77277520	GTCCCCACATGCGAC[C/T]AAAAAAGAAAAATCT	23077
rs137929772	snp	G/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77168768	TTTTCCACTAGTTAA[G/T]TTTTTGTCCAAAGAG	23077
rs137933465	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77182804	AGTGCACTGCTGAAT[A/G]TAAGTGGTGAGTGTA	23077
rs137933490	snp	A/T	0.00874735	0.0655527	intron-variant	MYCBP2	GRCh38.p7	13:77130388	TTTACTGTTTTCTAG[A/T]TCTATATTTTCCATA	23077
rs137952837	snp	A/C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77178610	ACTTTGGGTTGAAAT[A/C/T]GCTCTTTTTATTTAC	23077
rs137962761	snp	A/G	0.0422008	0.138995	intron-variant	MYCBP2	GRCh38.p7	13:77271692	TGCCATCCACGTAAG[A/G]CATGACTTGCTCCTC	23077
rs137964601	snp	C/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77310425	GTAAATAAAGTTATA[C/T]TGGAACACAGCCATG	23077
rs137965695	snp	A/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77323108	TGATTCATTTAATCT[A/T]CAAAACAATTCATGT	23077
rs137967857	snp	A/T	1.64966e-05	0.00287194	missense	MYCBP2	GRCh38.p7	13:77180155	GCTGACGCTGTCAGT[A/T]CACTGACAATGCTGG	23077
rs137978096	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77096090	GTCAATAAGGCATAT[A/G]TAGCAGAGGTTATCT	23077
rs137984313	in-del	-/T	0.00716266	0.059414	intron-variant	MYCBP2	GRCh38.p7	13:77296523	AATGGTTTAATTATA[-/T]TTTTTAATCTTGGCA	23077
rs137998662	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77147236	GAATGAGAATCACTA[C/T]ACTCAGGGCAGTGGT	23077
rs138001580	snp	A/G	0.0146672	0.084371	intron-variant	MYCBP2	GRCh38.p7	13:77235097	CTAATTTATTCACCA[A/G]ATTTTCTGATTATCT	23077
rs138041898	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77164260	GTGTCCATGTGCGTG[C/T]GTAAATTAAAAAAGG	23077
rs138046283	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77252383	TGAAGACGGTAATAC[C/T]GAGCTGTTATGAAGC	23077
rs138065722	snp	C/T			synonymous-codon	MYCBP2	GRCh38.p7	13:77098991	GGCTGGTTTAGAAGA[C/T]GTTGAGATGTTTCCT	23077
rs138066103	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77306111	TATTTGTAGATAATT[A/G]TATTTATAGAAAATA	23077
rs138088729	snp	C/T	0.00517822	0.0506191	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77077877	AAAAATTACATAATA[C/T]GTAACTTCACACTTG	23077
rs138118779	in-del	-/CA			intron-variant	MYCBP2	GRCh38.p7	13:77131519	AACAAACACACACAC[-/CA]ACACACACACACACT	23077
rs138130811	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77218932	ACTAGGAGCAGTGCA[A/G]AGTGAAAGAGATGGT	23077
rs138164811	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77213358	CATGGGCCTGTAATC[C/T]CAGCTACTCAGGAGG	23077
rs138180895	snp	A/T	0.000153988	0.00877328	missense, intron-variant	MYCBP2	GRCh38.p7	13:77233218	AGTCTGGCTAGAGCC[A/T]GTTCTCGATGGTTCA	23077
rs138183340	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77073082	ATATGTGCAACTATC[A/G]TCGTCAGTCAATATT	23077
rs138202943	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77122798	TGCAATTCTGCTAAA[C/T]CAGTGGTACTGTATA	23077
rs138216698	snp	C/T	5.1093e-05	0.00505409	intron-variant	MYCBP2	GRCh38.p7	13:77068883	GGTTAGTTTGATTTA[C/T]TACTCCTAGCAAAAC	23077
rs138220917	snp	A/C/G	8.38604e-05	0.00647491	synonymous-codon, missense	MYCBP2	GRCh38.p7	13:77097482	CTGGGCCATCTCTCC[A/C/G]AACAAATTACCCCTG	23077
rs138230973	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77158391	GCCAGTCCTCTATAT[A/G]TTATGTCCTCATTTT	23077
rs138270620	snp	C/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77208490	TCACTGATGGGCAAA[C/T]AGTTAAGTATATTTG	23077
rs138274825	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77300874	GGTGGAAGAGCACTT[C/T]CAAGGCAGCTGAGAC	23077
rs138275817	snp	C/G	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77285310	TGTGACTCACACATA[C/G]ACAGAATTGGTATTC	23077
rs138314951	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77154614	AGTATGAACATGGTA[G/T]TAGAATGTTGTCACA	23077
rs138323978	snp	A/C	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77056649	CAAACACCAGAGGAT[A/C]ATTCTTCTTTTTGGT	23077
rs138328025	snp	A/C	0.0182019	0.0936463	intron-variant	MYCBP2	GRCh38.p7	13:77318944	CTGCAAAAATATGAC[A/C]TCATCAAAAGAAATG	23077
rs138344561	snp	A/G	0.00676609	0.0577691	intron-variant	MYCBP2	GRCh38.p7	13:77106015	GATAATAATAAAACC[A/G]TGTAACTTTTCTTTC	23077
rs138347513	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77195847	TACTTTCTTAATCTA[A/C]AATTATTCCTTGGTT	23077
rs138354076	snp	A/G	0.0596104	0.162024	intron-variant	MYCBP2	GRCh38.p7	13:77200316	GATGAAATAAATGAA[A/G]TGAAGCGAGAAGGGA	23077
rs138366975	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77295760	AAATGTTCAGTATAA[A/G]AAAGATGGATTTTAT	23077
rs138419360	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77172307	AATGAAGACATGTAT[A/G]GCTGGAAGAAAAGGA	23077
rs138435094	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77052253	GCCCAGGCTGGAGCA[C/T]AGTGGCGCAATCATG	23077
rs138444193	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77142697	ATGTTAATGTAGATT[C/G]TGTGAATGTCTCAAG	23077
rs138454562	snp	A/T	0.00874735	0.0655527	intron-variant	MYCBP2	GRCh38.p7	13:77100816	ATACAGTATTAACAG[A/T]TGGGGCTAAGTTTTG	23077
rs138483052	snp	C/T	0.0240643	0.107019	intron-variant	MYCBP2	GRCh38.p7	13:77152763	TGAGAGCCACTTCCA[C/T]CGTTTGATAAAATCC	23077
rs138485010	snp	A/T	0.0244538	0.107838	intron-variant	MYCBP2	GRCh38.p7	13:77096660	ACTTGATCAAAAAGC[A/T]ATCAATTAAATGATG	23077
rs138487892	snp	C/T	0.0256215	0.110247	intron-variant	MYCBP2	GRCh38.p7	13:77239033	GCCGAGGCAGGAGAA[C/T]CGCTTGAAACCGAGA	23077
rs138513121	snp	C/G	0.00795532	0.062565	intron-variant	MYCBP2	GRCh38.p7	13:77236438	GATATATTTCAAGAT[C/G]ATAAAAATTATTATC	23077
rs138514850	in-del	-/AC			intron-variant	MYCBP2	GRCh38.p7	13:77316651	GGAAAGTGGGTCAAA[-/AC]CCACAGCCCCAGCCA	23077
rs138515040	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77095298	GAACTACCCTAGATA[C/T]CAATAAACAATCGCT	23077
rs138522394	snp	C/T	0.000153988	0.00877328	synonymous-codon	MYCBP2	GRCh38.p7	13:77098073	TCTGGCACATTCGGC[C/T]ACAGAAGGAGACATG	23077
rs138526126	snp	C/T	0.000153988	0.00877328	missense	MYCBP2	GRCh38.p7	13:77177830	ACAACTATTCCAGGT[C/T]TGTCTACTGAAAAAC	23077
rs138528311	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77090915	TACAAAGTTATTAAG[A/G]GAGCTATACAATTTC	23077
rs138535884	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77177487	GCTGGGATTACAGGC[A/G]TGCGTTGTATTTTTC	23077
rs138539424	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77147792	TGAAAGAAGAGACCA[C/T]ATTTCATCTTTCCAT	23077
rs138539756	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77188762	TTAAAATCATAGGCC[A/G]ACACCTCCATTTTTC	23077
rs138546129	snp	C/T	0.000100702	0.00709511	missense	MYCBP2	GRCh38.p7	13:77099007	GTTGAGATGTTTCCT[C/T]GATCACCTGTATGGT	23077
rs138551080	snp	C/G/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77283866	TCACGCCACTGCACT[C/G/T]CAGCCCCAGTGACAG	23077
rs138554155	snp	G/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77230856	GTCACAGGAGGTCAG[G/T]TGTGGAATTTCCCAC	23077
rs138587675	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77290411	ACAAAAACCAGTACA[C/T]GAATGTTCGTAATAG	23077
rs138588879	snp	C/G	1.64991e-05	0.00287215	synonymous-codon, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77083148	AGCTTCCCCGGCAAT[C/G]ACTATGTCTGAGAGT	23077
rs138593208	snp	A/G	0.0267878	0.112589	intron-variant	MYCBP2	GRCh38.p7	13:77117882	TGATCAATTTAACAT[A/G]TTAGGAACAACAACA	23077
rs138600326	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77209324	CTTAGTTATACTGTT[A/G]TTGCTAACTTAGTGA	23077
rs138620131	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77223897	GCACGATCATGTCAC[A/G]AACTAAAACTAAAAC	23077
rs138623147	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77259776	CATATTTATCACACA[C/T]AAAATCCTTCCAAGT	23077
rs138640240	snp	G/T	0.0182019	0.0936463	intron-variant	MYCBP2	GRCh38.p7	13:77135968	AGCCTCCTGAGTAGC[G/T]GGGACTATAGGCGTC	23077
rs138642704	snp	A/C/T	0.011919	0.0763696	intron-variant	MYCBP2	GRCh38.p7	13:77306594	TGAGGGGAAGAGAAC[A/C/T]CTCTGAAAAGCTTTG	23077
rs138653964	snp	A/G	0.0376037	0.131863	intron-variant	MYCBP2	GRCh38.p7	13:77301181	GCACTTTGGGAAGCT[A/G]AGGCGGGCAGATTAC	23077
rs138681893	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77213924	GTTCTCTCCACCCAC[C/T]GGCTACTGCAAACCT	23077
rs138693855	snp	A/G	0.0146672	0.084371	intron-variant	MYCBP2	GRCh38.p7	13:77062398	TAAATAAAAGCCCCT[A/G]AAGTTTCCATATACT	23077
rs138700076	snp	A/G	0.000153988	0.00877328	missense, utr-variant-5-prime	MYCBP2	GRCh38.p7	13:77278760	CCTTGGCTCTTACCT[A/G]GGACCTCAGGTGGCT	23077
rs138702517	snp	C/T	1.6525e-05	0.00287441	missense	MYCBP2	GRCh38.p7	13:77267895	GGCTTATCCTTATGG[C/T]TGTCATGCTGTGGTT	23077
rs138799004	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77116709	TGGTAAATAAAGTGG[C/T]GGTACTGATAACACA	23077
rs138802594	snp	G/T	0.000115516	0.007599	synonymous-codon, utr-variant-5-prime	MYCBP2	GRCh38.p7	13:77225511	GCCTGGAGGGTATGT[G/T]GTGATTTTGCTTGCA	23077
rs138813052	snp	A/G/T	0.000560889	0.0167375	synonymous-codon, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081894	ACTCTCTTCACTATC[A/G/T]CCATCATCTGACTTT	23077
rs138819877	snp	C/T	0.0263992	0.111815	intron-variant	MYCBP2	GRCh38.p7	13:77111303	GCTAAGTCATCCAAC[C/T]GAACTCATTTTTCCT	23077
rs138837742	snp	G/T	5.02871e-05	0.00501408	missense	MYCBP2	GRCh38.p7	13:77171633	CTCCATCAAATTCAC[G/T]CCTGTAGCATGAGCA	23077
rs138865949	snp	G/T	0.0244538	0.107838	intron-variant	MYCBP2	GRCh38.p7	13:77163493	TAAAGATGGATTTTG[G/T]GGGGGTAAGAAAATA	23077
rs138866254	snp	C/T	0.00438332	0.0466095	intron-variant	MYCBP2	GRCh38.p7	13:77106380	ACATTCAATAACAAT[C/T]TGCTAAATTATTGGC	23077
rs138869496	snp	C/T	0.000971441	0.0220176	missense	MYCBP2	GRCh38.p7	13:77067654	CAGCTGTTCCAGTGA[C/T]GGTGGTTCCTTTGGC	23077
rs138907688	snp	C/T	0.0614824	0.164198	intron-variant	MYCBP2	GRCh38.p7	13:77245599	CATCACATACTGGGG[C/T]CTGTTGGGGGGTGGG	23077
rs138908012	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77304893	ATGCTGCCCATAAAT[C/T]TGACAAATAAAATGG	23077
rs138910267	in-del	-/T	0.0225045	0.103662	intron-variant	MYCBP2	GRCh38.p7	13:77102132	TAAATGACCCATACA[-/T]TTTTTTCATGCCCAA	23077
rs138921032	snp	A/C	0.00159617	0.0282053	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77078680	TTCCTATGTTTTGGA[A/C]CACTTGTCAATTTAG	23077
rs138925101	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77167956	AAAAAACAAAGAATA[C/T]GGATTTTGAATACTC	23077
rs138927713	snp	A/G	0.000153988	0.00877328	synonymous-codon	MYCBP2	GRCh38.p7	13:77158068	TGGTGAATGAGAAAG[A/G]GCTAGACCCTTTCCA	23077
rs138946380	snp	A/C	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77318477	CTACAAATACTGGGC[A/C]AGGCGCAGTGGCTCA	23077
rs138957893	snp	C/T	0.0414363	0.137845	intron-variant	MYCBP2	GRCh38.p7	13:77152996	AGTGAACCCAGGAAG[C/T]GGAGCTTGCAGTGAG	23077
rs138965285	snp	A/G	0.00755907	0.0610114	intron-variant	MYCBP2	GRCh38.p7	13:77219315	CTCGATTTAGCAGAA[A/G]GAGGTCTCTTTGGTG	23077
rs138976175	snp	C/G	0.0185938	0.0946107	intron-variant	MYCBP2	GRCh38.p7	13:77309847	GGCTGGGCGCAGTGG[C/G]TCACGCCTGTAATCT	23077
rs138979222	snp	C/G/T	0.0326909	0.124155	intron-variant	MYCBP2	GRCh38.p7	13:77278348	GTTTTGTTTGCCCCC[C/G/T]GCTTCATCATACTAA	23077
rs139012619	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77236831	TGGGCCCAGTTGTTC[A/G]AGGCCAGCCTGGGCA	23077
rs139018163	snp	A/T	0.00597247	0.0543191	intron-variant	MYCBP2	GRCh38.p7	13:77323991	CCCTCTCTCACTTCT[A/T]CACTCTGTCTCTCCA	23077
rs139024119	snp	C/G	0.0189856	0.0955633	intron-variant	MYCBP2	GRCh38.p7	13:77297509	GGGAGGAGGTTGTTC[C/G]AGATGCTGAAGGGGT	23077
rs139043935	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77079872	TGCTCAACCTATAAC[A/G]TAGAGGAAGCCTGTT	23077
rs139088786	snp	A/G	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326005	TGGAAAGGGCTGGAA[A/G]GAATGTCATGGGAGA	23077
rs139104264	snp	A/G	0.000214385	0.0103512	missense	MYCBP2	GRCh38.p7	13:77098906	GATCAGCAGTAGTCC[A/G]GCTCATACGTCCATC	23077
rs139114119	snp	C/T	8.25076e-05	0.00642238	missense	MYCBP2	GRCh38.p7	13:77098300	ATTCACTGCTGTCAT[C/T]GCAGGTGCTGTCTGT	23077
rs139114452	snp	A/G	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77162257	TAGTGTATTCGTTTT[A/G]TCTAAAAAAAGAGGG	23077
rs139139112	snp	A/T	0.0256215	0.110247	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77292077	GACTAACAAGATATG[A/T]CTGTGTGACCAAACC	23077
rs139141565	in-del	-/C	0.00953873	0.0683987	intron-variant	MYCBP2	GRCh38.p7	13:77241437	TTCATTCATGTCGCT[-/C]AACCTAATATTTCTA	23077
rs139218239	in-del	-/AAAAAACCC			intron-variant	MYCBP2	GRCh38.p7	13:77213012	CACAGCAAGAAAACA[-/AAAAAACCC]CAGCCACAAACTAAC	23077
rs139220239	snp	A/C	6.60219e-05	0.00574513	missense	MYCBP2	GRCh38.p7	13:77097756	GTTTTCCCATCCTCA[A/C]ATTTTTCATGCAGAG	23077
rs139222388	snp	C/T	3.30224e-05	0.00406326	missense	MYCBP2	GRCh38.p7	13:77139332	ACACCATCATCATTA[C/T]GGATCTATAGAAAAA	23077
rs139223461	snp	A/G	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77156529	TGTGCATAATTTGAA[A/G]TCCTGAGCAGGCTCA	23077
rs139238905	snp	A/G	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77124689	CTAGTGGTGAGCACA[A/G]TTCTTTAGGAACACA	23077
rs139244139	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77105088	AGCCTCTGAATGGAA[A/G]AGTTAATTCAGGGGG	23077
rs139244174	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77052509	GGCCTAAAGCTATTT[C/T]GACTCTCAAATGGAT	23077
rs139250824	in-del	-/C			intron-variant	MYCBP2	GRCh38.p7	13:77222635	CAAGGACCACTCCCC[-/C]ACCCCTGTCCCACCC	23077
rs139261875	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77195314	TAAAAAGTCTGAAAT[A/C]GGCCAGGCCTGGTGG	23077
rs139292704	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77312179	AAAGTAAAATAAATA[C/T]ATTCTCAAAGAAAAA	23077
rs139300280	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77189465	CAGATTGCACGGTGC[A/G]TAAAAACCAAACAAA	23077
rs139303777	snp	C/T	0.000313322	0.0125125	synonymous-codon	MYCBP2	GRCh38.p7	13:77098184	TCTATTAGCACATTT[C/T]CGACTTATTTTGGGA	23077
rs139326012	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77196794	GAGAGTCACGTGGAG[A/T]CACAGCGTAGGCTGT	23077
rs139330477	snp	G/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77237845	AAATTCTTCATATAA[G/T]ACTTTAATTTAAAAA	23077
rs139336865	snp	C/T	0.0154538	0.0865337	intron-variant	MYCBP2	GRCh38.p7	13:77101880	AAAAATTGTATGTTG[C/T]GGCTGCTCAAAATAC	23077
rs139346993	snp	A/C	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77166225	AGTAGGTCTTTAATA[A/C]ATTTCTCTAAAAATT	23077
rs139348989	snp	A/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77255875	ATTGGTACTTTAACC[A/T]AAGTTCAACGCTTAG	23077
rs139385593	snp	A/C	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77179744	CAGAGCTGAAGTCTA[A/C]ACCTCATTACCTTTC	23077
rs139391125	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77239351	AGAAATAAAAGATCT[A/G]TATGTATGGCAGCCG	23077
rs139409100	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77092960	TTTAATTCCTTCACT[A/G]GTTGATCTCTTCTCT	23077
rs139432268	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77231778	ATATATTTGGGGGAA[A/G]AAAGAAACTGAAAAA	23077
rs139454502	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77246885	ACATGATCATCTCAA[C/T]TGATGTACAAAAAGC	23077
rs139471339	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77114294	AGAAGGACTTTTTCT[A/G]TATTTTCCTCAAAGC	23077
rs139472835	snp	C/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77123295	ATGATCACCAAATAT[C/T]CATATTTATGTCTGT	23077
rs139522142	snp	A/G	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77255202	ATCTATGTTTTCCAT[A/G]GTTGCTGTACTAATT	23077
rs139561281	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77249358	TATTCTGATATATTC[A/T]GTTTGCTTCATTCAT	23077
rs139570825	snp	C/T	0.000153988	0.00877328	synonymous-codon, utr-variant-5-prime	MYCBP2	GRCh38.p7	13:77288197	CTCTTTGGATTCCTC[C/T]TCTTCATCACTATCT	23077
rs139610742	snp	A/G	0.00716266	0.059414	intron-variant	MYCBP2	GRCh38.p7	13:77063513	CAGTGAGCCAAGATC[A/G]TACCATTGCACTCCA	23077
rs139619886	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77059471	CTGTATGAAGTAAAG[A/G]TGTCACAGGGGAACA	23077
rs139643090	snp	C/T	0.0146672	0.084371	intron-variant	MYCBP2	GRCh38.p7	13:77150399	TTCCCTCCTTGGCCT[C/T]CCAAAGCCCTGGGAT	23077
rs139650163	snp	A/G	0.00557542	0.0525036	intron-variant	MYCBP2	GRCh38.p7	13:77109144	TGGCAGGTAGAGGAC[A/G]GTTTCCTTAGTTCTC	23077
rs139655587	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77321372	AGGATTCCACTGATA[C/T]AACAGCTACATGAAG	23077
rs139664293	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77197129	GCTGAGGCTTGACTA[C/T]TGAATTTAGCAATAT	23077
rs139670540	snp	C/T	0.00914312	0.0669923	intron-variant	MYCBP2	GRCh38.p7	13:77221213	CGTATTTCATGAAGA[C/T]GATAAATTCAAGCAA	23077
rs139678705	snp	C/G	0.000280804	0.0118458	missense	MYCBP2	GRCh38.p7	13:77257792	TTTGCCCATAGCTAC[C/G]TGAGTTACAAAATGG	23077
rs139711839	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076004	CAAGGTGATTATTTG[C/T]AGCATTTAAAGACAC	23077
rs139713487	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77131834	CTAAATTAATGAACA[C/T]CAAATTGCAACTCTA	23077
rs139725026	snp	A/G	0.0275645	0.114116	intron-variant	MYCBP2	GRCh38.p7	13:77144251	CTACAGTGCCTGGGC[A/G]GACACCAGAAATTAT	23077
rs139729113	snp	A/G	3.33912e-05	0.00408589	synonymous-codon	MYCBP2	GRCh38.p7	13:77186025	GACTAAGGTGGTCCA[A/G]CTCCAGTGAAGAATA	23077
rs139732400	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77125964	ATGAATGGGAACAAA[G/T]AAATGAAACCTTTTG	23077
rs139739967	snp	A/C	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77215874	GTATGAGCCACCACA[A/C]CTGGCCTATGATTTC	23077
rs139745277	snp	A/G	0.00478085	0.0486577	intron-variant	MYCBP2	GRCh38.p7	13:77268776	AAGAGCAAAACTACA[A/G]CTCCAAAAAAAAAAA	23077
rs139759478	snp	A/C/T	0.00209905	0.0323299	intron-variant	MYCBP2	GRCh38.p7	13:77267806	CACATTTCTTAAAAT[A/C/T]GCTTGTGGAGAAAAA	23077
rs139766052	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77069947	GATATTTTTATGTTA[C/T]GTAGCACCCCATTAT	23077
rs139774533	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77054825	TGGGTGGTCTCAAAC[G/T]CCAGAGCTCAAGAAA	23077
rs139795202	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77065297	TGAGAAAATATCCAC[A/G]CTGTTGGGAAAAGTG	23077
rs139807000	snp	A/G	0.021333	0.101051	intron-variant	MYCBP2	GRCh38.p7	13:77287244	AGGCCGGAGTGCAAT[A/G]GCATGATCTCGGCTC	23077
rs139807523	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77210080	AAAGAAGTGCTCAGC[C/T]CTGTGATGAGCCACT	23077
rs139851956	snp	C/T	3.29826e-05	0.00406082	missense, intron-variant	MYCBP2	GRCh38.p7	13:77126427	CCCGTCTTCACTACC[C/T]TGTACATGCCTGGCC	23077
rs139852725	snp	A/G	5.02812e-05	0.00501379	missense	MYCBP2	GRCh38.p7	13:77185114	TTACCTGATCCAAAC[A/G]ATTCAGCAGATCACA	23077
rs139859461	snp	A/C	0.00119737	0.0244387	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77085814	GAAAGAGTCATTCCT[A/C]TCAGTGGAGCCTTGC	23077
rs139859896	snp	C/T	0.00914312	0.0669923	intron-variant	MYCBP2	GRCh38.p7	13:77211043	ACTGAGACAGAATTG[C/T]AGTTATTAGATAAAC	23077
rs139872031	snp	C/G	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77303515	GGACTGAATGATAAG[C/G]TAATTCTCTGGTCAT	23077
rs139897314	snp	C/G	0.0263992	0.111815	intron-variant	MYCBP2	GRCh38.p7	13:77139920	ACATTCTATAAAATA[C/G]TTTTAAAATATTTCC	23077
rs139900344	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77086119	TGCCCTCATATTTAC[A/G]CTTTCTTTTCTCTTC	23077
rs139908095	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77241385	AAGGATGTGCTATAC[C/T]GTAGTTTAAATGTAA	23077
rs139912388	snp	C/G	1.65359e-05	0.00287536	missense	MYCBP2	GRCh38.p7	13:77098440	TCTGTAGAATCCTTT[C/G]GTACTGATTTTGGTT	23077
rs139930687	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77155503	AATCACAAATAATTA[C/T]GTATAATATGCTCTG	23077
rs139931694	snp	A/T	0.0236746	0.106192	intron-variant	MYCBP2	GRCh38.p7	13:77099595	TAGACTAGTTTACAA[A/T]GAGCACATGAATGCC	23077
rs139939362	in-del	-/AAGTG	0.0543475	0.155628	intron-variant	MYCBP2	GRCh38.p7	13:77059117	ATCCACATTCTTATT[-/AAGTG]AATTGAGAAACCAAA	23077
rs139940323	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77138622	AGCAATCTTGTGAAC[A/C]CTGGCTCTATTCTAC	23077
rs139940806	snp	C/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77226236	TTTCACTCCTTCTTT[C/T]CTCCTCCCTTCTCAC	23077
rs139943687	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77278974	AACACTTTCTAAGCA[A/G]TTTAGTTGGTACAAG	23077
rs139951153	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77151258	GTGGAATGAATCTAC[A/G]TTAAGTTATTGCAGG	23077
rs139952272	snp	A/G	0.0146672	0.084371	intron-variant	MYCBP2	GRCh38.p7	13:77238019	GAGGCCAAGGCAGGC[A/G]GATTACAAGGTCAGG	23077
rs139954555	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77297113	AAAATCCCCAGCTCA[C/T]ATACTTTATGTCTCC	23077
rs139973023	snp	C/T	0.00597247	0.0543191	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77292911	GCAGTGAGCTGAGAT[C/T]GCACACCACTGCACT	23077
rs139975510	in-del	-/CA/CACA	0.163048	0.239529	intron-variant	MYCBP2	GRCh38.p7	13:77264867	CAAGCAAGTTAAAAG[-/CA/CACA]CACACACACACACAC	23077
rs139981698	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77324895	TAAAGATGTTCCTGC[A/G]GTGCCATAATTTAGA	23077
rs139983670	snp	A/G	0.0146672	0.084371	intron-variant	MYCBP2	GRCh38.p7	13:77273796	CAATTACTTTGCTTT[A/G]GTTTCTTTCTAGTTA	23077
rs140020103	snp	C/T	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77308173	GCTACTTCAAAATCC[C/T]TCCCCTACCCATCAA	23077
rs140025108	snp	G/T	1.65529e-05	0.00287683	missense	MYCBP2	GRCh38.p7	13:77171611	CTCAGAAGTTGGGAT[G/T]GTAAATCTCCATCAA	23077
rs140029202	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77181025	TGTGTAAATCACTTT[C/T]TTAACAAAATTCTTT	23077
rs140060369	snp	C/T	0.000153988	0.00877328	synonymous-codon	MYCBP2	GRCh38.p7	13:77045438	CTCTTCCCCAGTGGG[C/T]GGATGAACAACATGG	23077
rs140078246	snp	A/G/T	0.000395328	0.0140541	missense, synonymous-codon	MYCBP2	GRCh38.p7	13:77058314	ACTTTTGTCACAGCC[A/G/T]TGTAGACAGGGCAGA	23077
rs140096667	snp	C/T	0.0271762	0.113356	intron-variant	MYCBP2	GRCh38.p7	13:77102982	AAGTAAGAGTAATGT[C/T]TAACCTATAGATGTA	23077
rs140142289	snp	C/T	0.00597247	0.0543191	intron-variant	MYCBP2	GRCh38.p7	13:77119865	AGGTAGCTGGGACTA[C/T]AGGCATGAGCCACTA	23077
rs140142475	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77172840	TGGTTAAGGGTGTAT[A/C]ACCTGAAATCTGACT	23077
rs140146141	snp	C/T	0.0399052	0.1355	intron-variant	MYCBP2	GRCh38.p7	13:77056073	AAAGTTACCTTGTTG[C/T]CACAAATAAGACACG	23077
rs140160000	snp	G/T	0.0119091	0.0762411	intron-variant	MYCBP2	GRCh38.p7	13:77146956	TACAGAATGTTTATT[G/T]CAGTACAGTTTATAA	23077
rs140164433	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77264292	GTAAACATGCACCAC[A/G]ATGAACAAACTATAA	23077
rs140184460	snp	C/T	0.0279526	0.114869	intron-variant	MYCBP2	GRCh38.p7	13:77311671	ATAAGAAAATGGAGA[C/T]GGGAGAAAAGAGTCT	23077
rs140225013	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77182683	GCCCCTGGAAATTGA[C/G]TGGTAAAACATACTA	23077
rs140227340	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77238830	CTGAGCAAGGCTTTA[A/G]TACAAGAACTAGGGC	23077
rs140246419	snp	C/G	3.35661e-05	0.00409657	missense	MYCBP2	GRCh38.p7	13:77205558	TGTACTTGCAACACC[C/G]ATTTTTAAGTCCTGC	23077
rs140250757	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77322803	ATACCACCATTCACA[C/T]TCAGAACAGATCATA	23077
rs140280767	snp	C/T	0.000252094	0.0112242	synonymous-codon, nc-transcript-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087559	TGGTGCAGGAGTCAG[C/T]GATGCCACAAAATGC	23077
rs140285290	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77213074	AGAACCAGGGAAGGA[A/C]ACATGGCAAGCACAT	23077
rs140293207	snp	C/T	0.0256215	0.110247	intron-variant	MYCBP2	GRCh38.p7	13:77305134	GACTCTTTTAGACAA[C/T]ATAAAAAGAAGAAAC	23077
rs140298631	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77318444	GGAAGAAAAATATTT[G/T]TATTTCCTTCTTAAA	23077
rs140311566	snp	C/T	0.000822444	0.0202619	synonymous-codon, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77078827	AATTTCAATTACCTG[C/T]TTTATTCTGCACAAA	23077
rs140315999	snp	A/G	4.94295e-05	0.00497115	synonymous-codon	MYCBP2	GRCh38.p7	13:77070682	TATGATTCCAACCAT[A/G]TGTTCTTTCAGGTCA	23077
rs140316142	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77161457	GCCCTAACCACTTAA[C/T]ATGACATACTGGTTT	23077
rs140321042	snp	C/G	1.67416e-05	0.00289318	intron-variant	MYCBP2	GRCh38.p7	13:77088786	ATAGAATCATCACAT[C/G]ATTTGTATAATCAAT	23077
rs140357805	snp	C/T	0.0333695	0.124785	intron-variant	MYCBP2	GRCh38.p7	13:77141598	CACCATAGTGAAACC[C/T]CATCTCTACTAAAAA	23077
rs140361083	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77210482	CAGGCGTGAGCCACC[A/G]CACCCGGCCCAGCAC	23077
rs140369025	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77303131	TGAGGTCAGGTGTTC[A/G]AGACCAGCCTCACCA	23077
rs140370311	snp	A/G	0.00438332	0.0466095	intron-variant	MYCBP2	GRCh38.p7	13:77050369	GTAAAATTCTCTCCT[A/G]TGGTTGCACGGACCT	23077
rs140372040	snp	A/G	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77229363	AAACTAAGGCTTGAA[A/G]GGTTAAGGGGTTAAG	23077
rs140397633	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77282650	GTGATAACTCCCAAA[G/T]CTATTTTTCTAGCTG	23077
rs140406161	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77297981	CCTAACTCAACTTTT[A/G]AAGACACAAACCTGA	23077
rs140443023	snp	C/T	0.0123036	0.0774623	intron-variant	MYCBP2	GRCh38.p7	13:77300348	GTTGCAACTACTCAA[C/T]GGTTACAGCACGAAA	23077
rs140449422	snp	C/G	0.000181538	0.00952554	synonymous-codon, nc-transcript-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076835	AGCATCTCCAGAGAT[C/G]AGCTTTCCAAATACC	23077
rs140450381	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77045757	GATCACTTCGAGCTA[C/T]AGATCTTTTTCTATT	23077
rs140450758	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77100246	AAAATGTTTTTTATG[C/T]TTCCGTGCATGTGTT	23077
rs140452628	snp	C/T	0.0611083	0.163768	intron-variant	MYCBP2	GRCh38.p7	13:77187901	CATGGTGAAACCCCC[C/T]CTCTACTAAAAATAC	23077
rs140458711	snp	A/G	0.027039	0.113086	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77082022	ATATAAGCAATATAC[A/G]AAATAATTATTTTCC	23077
rs140488606	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77117303	GCTAGAAATTGATAG[C/T]ACTTATATTTCCAAA	23077
rs140494245	snp	C/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77208194	CTGAAGGCCTCAAAC[C/G]TCTTCAGAAAAAGTA	23077
rs140528841	snp	C/T	1.66538e-05	0.00288559	synonymous-codon	MYCBP2	GRCh38.p7	13:77097401	CATGTGATAGGTCAC[C/T]GGGTATGGATGTGAC	23077
rs140552075	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77164682	TAAATTGAGAGTAGA[C/T]GAGATTCAGTACTCA	23077
rs140587080	snp	C/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77258438	TCAACTCTAAATTGA[C/T]TGAAGCATCTTTAAC	23077
rs140609762	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77244116	TTTAAAGAAAAGATA[C/T]AAATAGCAGAATAAT	23077
rs140616447	snp	C/T	0.00478085	0.0486577	intron-variant	MYCBP2	GRCh38.p7	13:77251794	CCTCCAGTGACCTTC[C/T]AAGGTCTTCAGAAGA	23077
rs140639905	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075077	GCTGGGCACGGTGAC[A/G]TGCACCTGTAGTTCC	23077
rs140691735	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77072720	AGATATTAAAAAGAC[A/G]TAAGGGTATATTATG	23077
rs140730309	snp	G/T	0.00365453	0.04259	intron-variant	MYCBP2	GRCh38.p7	13:77050961	AAACTATGGTATATA[G/T]ATCATAATCGTGATT	23077
rs140735153	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77180495	GAAGTTCTTTTTTGA[A/G]TTATCTGTCTCTGCG	23077
rs140737867	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77121069	ATGATAAAAATCAAA[G/T]TTTACTAGATTTAGT	23077
rs140739745	snp	A/C	0.0119091	0.0762411	intron-variant	MYCBP2	GRCh38.p7	13:77068324	TCATGGTAATATGGT[A/C]ATCAGTAGCCAGAAT	23077
rs140746240	snp	C/T	0.000230985	0.0107443	synonymous-codon	MYCBP2	GRCh38.p7	13:77212125	CTTTGCATTCCAATA[C/T]GGCACATCCAAAATT	23077
rs140746287	snp	A/G	0.000153988	0.00877327	stop-gained	MYCBP2	GRCh38.p7	13:77190325	TTGAACTCTTGAACT[A/G]GAAAACAACCCTAAG	23077
rs140756301	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77100334	CTGCCCCAGTCTTTG[C/T]CAAGGGCAGGTATTT	23077
rs140758979	snp	A/G	0.0275645	0.114116	intron-variant	MYCBP2	GRCh38.p7	13:77188003	TTGAACTCAGGACGC[A/G]GAGGTTGCAGTGAGC	23077
rs140771286	snp	A/C/G	3.30033e-05	0.00406209	missense, synonymous-codon	MYCBP2	GRCh38.p7	13:77211232	ATCCTCTTGTTCTGA[A/C/G]TCATTAAAAGTTTTA	23077
rs140774945	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77232381	GTTCAAAGGCCAGGA[C/T]ACAAGGCAAAAATTT	23077
rs140777927	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77142270	TTCACAATCCTCATT[A/G]AAGTGTTAACACTTG	23077
rs140779604	snp	C/T	0.030278	0.119257	intron-variant	MYCBP2	GRCh38.p7	13:77239010	CTATAATCCCAGCTA[C/T]TCGGGAGGCCGAGGC	23077
rs140783759	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77328023	TTTGATTCCTACTAC[A/G]TTTTATCCTTTGACT	23077
rs140787103	snp	A/G	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77320280	AAGAGCTAGGGGAAC[A/G]TGTGCCTGAAAGCGG	23077
rs140790174	snp	C/G	0.0126979	0.078662	intron-variant	MYCBP2	GRCh38.p7	13:77229959	TCCTAACTATGTACA[C/G]TATTAACACATTTTT	23077
rs140798899	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77115208	ACTGTCAGAAGGTAC[A/G]GGACATAAAATGAAG	23077
rs140818937	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77135159	AAACAGTGCTGAAGG[C/T]AACTTTTCAGTACTT	23077
rs140826619	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77317242	CAGGCGTGAGCCATC[A/G]TGCCCAGCCTGGTGA	23077
rs140827899	snp	C/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77283188	CTGATGATATTCTTT[C/T]GCTTAAAATCTTCAA	23077
rs140837234	snp	C/T	0.000215348	0.0103744	utr-variant-3-prime	MYCBP2	GRCh38.p7	13:77045372	TAGACAAAGGATCTG[C/T]GTGTTCTAAAAAGTG	23077
rs140847422	snp	C/T	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77309500	ATAAGCCTGAGACAA[C/T]CAAAGAAGAAAATTC	23077
rs140865970	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77181382	TAGAATGTAAAGTAT[C/T]TGCAACTTACCTTCA	23077
rs140867336	snp	A/T	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228275	CTTTGGGAGGCTGAG[A/T]AAGGCAGATTACTTG	23077
rs140868200	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77275587	ACAGCTACTTGGGAG[C/G]TGGAGGCAGGAGGAT	23077
rs140888236	snp	A/C	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77321651	TTCCTACTGTTACCT[A/C]CATACAAACTGTGCT	23077
rs140899635	in-del	-/A	0.0460142	0.144533	intron-variant	MYCBP2	GRCh38.p7	13:77304953	AACATTAAACAAGGG[-/A]AAAAAAATGTAATAT	23077
rs140921504	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77277532	GACCAAAAAAGAAAA[A/T]TCTGACATGTAGTTA	23077
rs140926429	snp	C/T	0.0460142	0.144533	intron-variant	MYCBP2	GRCh38.p7	13:77218271	CTGTATACTGACTGG[C/T]CTGTTAGAGATCTTT	23077
rs140947279	snp	C/G	0.0263992	0.111815	intron-variant	MYCBP2	GRCh38.p7	13:77127841	TACATGACTGGTCAG[C/G]GAAAATGTTAAAGTC	23077
rs140992315	in-del	-/AAAAAAAAAAAC/AAAAAACC/AAAC/C/CC	0.000423924	0.0145537	frameshift-variant, cds-indel	MYCBP2	GRCh38.p7	13:77051098	CAAAACAGAAAAAAA[lengthTooLong]CAGCCACTGAACAGC	23077
rs140994741	snp	A/G	3.29516e-05	0.00405891	synonymous-codon	MYCBP2	GRCh38.p7	13:77068793	TTCACGGACTCTGGT[A/G]GCTTCCATGCGAATA	23077
rs141005456	snp	A/G	4.95152e-05	0.00497545	missense	MYCBP2	GRCh38.p7	13:77098711	ACAACCGAGAACCTG[A/G]TCCTGGGGATTCAGC	23077
rs141032332	snp	A/C/G	4.94885e-05	0.00497415	synonymous-codon, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77083142	ATGAGCAGCTTCCCC[A/C/G]GCAATCACTATGTCT	23077
rs141062318	snp	A/G	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77185019	TATACAAGTTAAGAA[A/G]ATATGGCAACTGCAA	23077
rs141065113	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77095207	AGTCATTATGTCAGT[C/T]AAGGCAACTCAAAAA	23077
rs141069068	snp	C/T	3.31181e-05	0.00406914	missense, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081612	TTTTTATGTCAACAA[C/T]GCTGGTTAAGTCCTT	23077
rs141111402	snp	C/G	3.29516e-05	0.00405891	missense	MYCBP2	GRCh38.p7	13:77158022	TTTGGATTTGGAGTG[C/G]TAAATTTCCCTCAAG	23077
rs141115025	snp	A/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77234281	ATTTGACAGGTTACC[A/T]TTAACTGAAACAGGA	23077
rs141115332	snp	C/G	0	0	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076523	TGATTACAAATGAAT[C/G]CAAAAACCCAAGGTA	23077
rs141123352	snp	C/T	0.0158469	0.0875917	intron-variant	MYCBP2	GRCh38.p7	13:77110774	AATAGAAAGAACCTA[C/T]GTTGAAATATTGGGG	23077
rs141143323	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77129301	CATCTGCAGAAGATG[C/T]GTGCACAGTAACAAC	23077
rs141146303	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77219453	AAAATGAAGCTGAAG[C/G]AGAGGATTTTTTTTT	23077
rs141151504	snp	C/T	0.000148568	0.00861752	MYCBP2	13	allele_origin=T(somatic)/C(germline)	13:77098150	GAAAACTCGATTTTT[C/T]TTTTTTGGGCCTGGT	23077
rs141153284	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77089361	TCATTTTCTAAAAGA[C/T]GGCTTTATAAGAAAC	23077
rs141155253	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77146025	CTATACATTATTATA[C/T]GACATCTCTATCGGC	23077
rs141165449	snp	C/T	0.000153988	0.00877328	missense	MYCBP2	GRCh38.p7	13:77095404	TTTTCACAGGAAGAT[C/T]CTCAGAAATGCCTTC	23077
rs141165815	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77271282	TTCTGAGCTCAAATG[C/T]AATAAATAGTGTTTT	23077
rs141180935	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77110001	CCATTATTGTACAAA[C/T]TGATTGTAAAACATG	23077
rs141238364	snp	A/G	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77073425	CCCAAAAAATCTACA[A/G]TTCACATCACACTTA	23077
rs141247876	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77304331	GTCATTTGCAGCACC[A/G]TGGATGAGCCTGGAG	23077
rs141282908	snp	C/T	0.0256215	0.110247	intron-variant	MYCBP2	GRCh38.p7	13:77212541	GTCACTTTGACATAG[C/T]AAGTTGATAGTATAA	23077
rs141317634	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77174961	TATATATTATATATA[C/T]ATATTTTTTTCTGAG	23077
rs141358281	snp	C/T	0.000153988	0.00877328	missense	MYCBP2	GRCh38.p7	13:77267933	TCTCTATATAATAAA[C/T]AACCCTGATAACAGC	23077
rs141360002	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77265958	CATTCTTCACCACTA[A/C]TACAGCACACACTTA	23077
rs141361966	snp	A/G	0.0345262	0.126772	intron-variant	MYCBP2	GRCh38.p7	13:77317735	CGAGGTCAGGAGTTC[A/G]AGACCATCCTGGTCC	23077
rs141384111	snp	C/T	0.000153988	0.00877328	synonymous-codon	MYCBP2	GRCh38.p7	13:77261175	ACTCAACTTACTTGA[C/T]TCTCCATCTTCTCCT	23077
rs141386907	snp	A/G	0.00283188	0.0375222	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77078775	GAAGGCTGAGAAGAA[A/G]AAATTTCTCTCTAGG	23077
rs141388278	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77116186	TTACTACATAGTGGC[A/G]ACTATCAGTATAAAC	23077
rs141401592	snp	A/G	0.0166325	0.0896639	intron-variant	MYCBP2	GRCh38.p7	13:77171732	ATCCTCATTTAATTT[A/G]TAGCTTTTTAAAAGT	23077
rs141406246	snp	C/T	1.67309e-05	0.00289226	synonymous-codon	MYCBP2	GRCh38.p7	13:77097476	TGCCAGCTGGGCCAT[C/T]TCTCCAAACAAATTA	23077
rs141452388	snp	A/G	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77149007	TCTATTTTTATATTC[A/G]GAGTATCTTTATTGT	23077
rs141454180	snp	A/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77314361	ACTTGGAAGCAACCC[A/T]ATTGTCCTCCAAACT	23077
rs141471964	snp	C/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77164213	ACACTATACCCACTG[C/T]CTGGCTCAAAGCATG	23077
rs141477685	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77166729	GGAGGAACAGAGTAA[A/G]GAGGACAGAGATAAA	23077
rs141479417	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291463	TGGAAAAGAGTTTTC[C/T]AGTTTCTTAAAAAGC	23077
rs141489190	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77073944	AATATTATTGACATG[A/G]CGATTCTCCCTAAAC	23077
rs141498635	snp	A/C	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77306782	GGAATGAGAGCAAGC[A/C]AATAACTAAGAACAC	23077
rs141514914	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77091998	GCACTGCACTCTGGA[A/G]AAAATGTCAAGAGCA	23077
rs141538124	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77231537	AGGCATGTGCCACTG[C/T]GCCCAGCCTCACTGA	23077
rs141553092	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77105118	GAATCCAACCTGCCA[A/G]TATAGGAAGGAATAC	23077
rs141601776	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77091199	CTCTAAGCTTATGTA[C/T]ATTCTTGTTTGAATA	23077
rs141604813	snp	A/T	8.25716e-05	0.00642487	synonymous-codon	MYCBP2	GRCh38.p7	13:77156076	CATATTGGGAACATG[A/T]ACCACATCCCCATAC	23077
rs141605192	snp	C/T	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77301708	AAGAAGCAAAATATG[C/T]GGCAGACACATAATC	23077
rs141608171	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77177594	CTCAAAGAGCTGAGA[C/T]TACAGGTGTGAGCCA	23077
rs141624966	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77172188	ATAGGAGTGAGCCGC[A/G]CACCCAGCTGACCTG	23077
rs141626388	snp	C/T	0.000264752	0.0115024	synonymous-codon	MYCBP2	GRCh38.p7	13:77165390	AAAAAGGGCCTCATT[C/T]CCTAATAAAAATGCC	23077
rs141640392	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	MYCBP2	GRCh38.p7	13:77044658	ACCTCCCACAGTGGT[A/G]GACTTTATCACTGTA	23077
rs141643874	snp	A/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77223753	AGCCAGCAAGCTGGG[A/T]AGAGAGAAGGACAAA	23077
rs141645188	snp	C/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77230916	TTTCAGATCTTGGAG[C/T]ATTTCGAATTTTCAA	23077
rs141648704	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77314769	TGGACTTGAGAGTGA[C/T]TATGATGTGTCAGTG	23077
rs141649596	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77172503	CTGTGCTGTAGAGAA[C/T]TGATTGTAGGAGACC	23077
rs141667910	snp	A/G	4.94474e-05	0.00497205	missense	MYCBP2	GRCh38.p7	13:77177836	ATTCCAGGTTTGTCT[A/G]CTGAAAAACAGATTG	23077
rs141687157	snp	C/T	0.00517822	0.0506191	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77086072	ACCATGACATATCAT[C/T]ACTTTTTACATAGTC	23077
rs141696339	snp	A/C/T	0.00953873	0.0683987	intron-variant	MYCBP2	GRCh38.p7	13:77128078	AATGTAAAATACGCA[A/C/T]TTTATATACTCATCA	23077
rs141701958	snp	C/T	0.000461148	0.0151777	missense	MYCBP2	GRCh38.p7	13:77125420	TCTCACAGAACTCTA[C/T]CATGCTGTTCTGATC	23077
rs141717634	snp	C/T	0.00107021	0.0231076	missense	MYCBP2	GRCh38.p7	13:77168483	CTCTCTATGACAGCA[C/T]AGTGACTGGAGGTTG	23077
rs141726107	snp	C/T	0.00438332	0.0466095	intron-variant	MYCBP2	GRCh38.p7	13:77167922	TATCCTTCTCTTCCT[C/T]AATTTGCATGATACA	23077
rs141738031	snp	C/T	0.125182	0.216612	intron-variant	MYCBP2	GRCh38.p7	13:77199192	GGTGTGCGCACCATG[C/T]GCGAGCTGAAGCAGG	23077
rs141742109	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77294791	AAGGGATACAGTGAA[C/G]AGATTATTTTTCTGC	23077
rs141744264	in-del	-/A	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77235517	CTTGGAGAGGTATGC[-/A]AAAAAAACAGATAAT	23077
rs141746740	snp	A/C/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77245995	TCAGCCCTTTCATAT[A/C/T]GATTGTGAACCATAT	23077
rs141772648	snp	G/T	0.00117623	0.0242225	synonymous-codon	MYCBP2	GRCh38.p7	13:77098970	CTCTGATTTTCCTGA[G/T]GTAGAGGCTGGTTTA	23077
rs141783311	snp	A/T	3.31807e-05	0.00407299	missense	MYCBP2	GRCh38.p7	13:77273587	AGGCAAGCACAGGAA[A/T]GTGCTGTTAAGGACT	23077
rs141784628	snp	C/T	0.0256215	0.110247	intron-variant	MYCBP2	GRCh38.p7	13:77288536	CCAACTTCTAGTCCC[C/T]TTTTCTATACCTCAC	23077
rs141785865	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77241715	TATCAATCAACATCA[C/T]TTATCAGATGCTATG	23077
rs141795465	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77246283	CAATTTGGAAGATCA[C/T]TTACTACACAGTAAA	23077
rs141830285	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77195388	GATCATATGAGGTCA[C/T]GAGTTTGACACCAGC	23077
rs141855928	snp	A/C	0.0138799	0.0821421	intron-variant	MYCBP2	GRCh38.p7	13:77189962	CATTTGAAATTAGTA[A/C]GAAAATCAATGGATA	23077
rs141878897	in-del	-/G	0.00993419	0.0697739	intron-variant	MYCBP2	GRCh38.p7	13:77296745	AAAGCTATCAAAAAT[-/G]GGTATTTCCAAAGTA	23077
rs141898987	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77239803	CAGCACCTGAAAGAG[A/T]GTCCTCCATCCAATT	23077
rs141912493	in-del	-/T	0.00755907	0.0610114	intron-variant	MYCBP2	GRCh38.p7	13:77068947	TGATACTCAATTTAA[-/T]ACTATTCTCCCAGTT	23077
rs141914753	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77117678	CATGAGAACTGAATG[C/T]CAAGAAGAACACACT	23077
rs141933651	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77049006	GCTGGTTATCTCCCA[A/T]GCTCCTCCAGGTCAT	23077
rs141934212	snp	C/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77062458	GTGAGATGAACTTGG[C/T]CGAAGGGACACAATC	23077
rs141936784	snp	C/T	0.00438332	0.0466095	intron-variant	MYCBP2	GRCh38.p7	13:77138114	TATTTTACTTATAGA[C/T]GTATCATTGTTCAAC	23077
rs141958299	snp	A/G	4.95511e-05	0.00497726	synonymous-codon, nc-transcript-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77083061	CTGTAATGAACTGCC[A/G]CTGGGGAGAGACATC	23077
rs141963129	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77278085	TGCTAAGTCAGAAGT[C/T]TAATCCATAACACAA	23077
rs141978651	snp	A/G	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77061902	TCGGAAGTCTATTAA[A/G]AATTTAGAATCTGAA	23077
rs141979695	in-del	-/ACACAC			intron-variant	MYCBP2	GRCh38.p7	13:77245745	CCAGAACGTAAAGTA[-/ACACAC]ACACACACACACACA	23077
rs141986739	snp	C/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77183843	ATGAGCCACCGTGCC[C/T]GGTGAACCCCTATTT	23077
rs142006501	snp	C/T	0.000236827	0.0108792	intron-variant	MYCBP2	GRCh38.p7	13:77058180	TATTCCCCATCTTAA[C/T]GTCTGGATACATTCA	23077
rs142015517	snp	A/G	9.89527e-05	0.00703325	missense	MYCBP2	GRCh38.p7	13:77059614	GCTTCTGAGCTACTC[A/G]TGGTGGGTTTGCCTA	23077
rs142015874	snp	C/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77066283	GTTATTTGAGTTCCC[C/T]TTCAAGTATTTCTCT	23077
rs142020119	snp	C/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77323576	ATGAAATAGGTTTTA[C/T]TGCCTTCACAGTTAC	23077
rs142034972	snp	C/T	0.000938542	0.0216423	missense	MYCBP2	GRCh38.p7	13:77067657	CTGTTCCAGTGATGG[C/T]GGTTCCTTTGGCTTT	23077
rs142045136	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77106774	TATTTTAGGTTCAAG[A/G]GGGACATGTGTAGGT	23077
rs142049232	snp	A/G	0.00597247	0.0543191	intron-variant	MYCBP2	GRCh38.p7	13:77196699	CAGTTAACTGGGATG[A/G]GGAAGAACATGAGGA	23077
rs142071043	snp	A/G	0.000153988	0.00877328	synonymous-codon, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081897	CTCTTCACTATCGCC[A/G]TCATCTGACTTTGAC	23077
rs142079611	snp	A/G	0.00918525	0.0671436	synonymous-codon	MYCBP2	GRCh38.p7	13:77194206	AAGAAGGTCACCATC[A/G]GTTTCATGATCTCCT	23077
rs142089567	snp	A/G			synonymous-codon	MYCBP2	GRCh38.p7	13:77098004	TAGGAAAGAAGAACA[A/G]GCCATTGCATCATGT	23077
rs142095220	snp	G/T	0.0422008	0.138995	intron-variant	MYCBP2	GRCh38.p7	13:77271696	ATCCACGTAAGACAT[G/T]ACTTGCTCCTCCTTG	23077
rs142099944	snp	C/T	0.0150606	0.0854603	intron-variant	MYCBP2	GRCh38.p7	13:77071200	CTTATTATGTGCACG[C/T]TGTTCTTCTAAGTGC	23077
rs142116713	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77152635	CAACTGATGAGACGC[A/G]CGGCTTAACCTCAGA	23077
rs142120541	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77119591	CTTGGACAGTATTAA[C/G]AGTTAAAATGGGAAC	23077
rs142123450	snp	C/T	0.00597247	0.0543191	intron-variant	MYCBP2	GRCh38.p7	13:77210763	TATAAACAGGATTGA[C/T]GACAGACTAAAAATA	23077
rs142125756	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77243250	TTCAAGAAAGTAAAA[A/G]CTAGCAAAAACATTG	23077
rs142132264	snp	A/C	0.00676609	0.0577691	intron-variant	MYCBP2	GRCh38.p7	13:77178998	TCTGAGGCCAAACTC[A/C]AAGTTAACCAAGAAA	23077
rs142155607	snp	A/G	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77222611	AAAAACTCTGATGCT[A/G]GCATCCTATCAAGGA	23077
rs142162370	snp	C/T	0.0130921	0.0798413	intron-variant	MYCBP2	GRCh38.p7	13:77050207	GGTAATTTTGAGAGG[C/T]ACTATTAAGCTGTTT	23077
rs142163517	snp	A/G	0.00835141	0.0640778	intron-variant	MYCBP2	GRCh38.p7	13:77141474	TAGGAAATAAATGAC[A/G]TAAAATGTACAAGGG	23077
rs142163972	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77313722	GACACATCTGATAAA[A/G]GACTGTTATCCAAAA	23077
rs142181383	snp	C/T	0.0166325	0.0896639	intron-variant	MYCBP2	GRCh38.p7	13:77267610	TCAGAGATTAGGCCA[C/T]AGACGGCCAAGTTTG	23077
rs142181650	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77155859	AAAATGTAAAGAACA[A/G]ACTCACAAAAAAAAC	23077
rs142185344	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77318624	CCGAGTGTGGTGGGA[C/T]ACGCCTGTAATCCCA	23077
rs142199953	snp	C/T	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77064267	CAAAGGACCTTCGGT[C/T]TATCACAGCATAATG	23077
rs142210215	snp	C/G	0.0256215	0.110247	intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77325770	AGATCACAAGAGTAA[C/G]TGCAACCTCATTTCT	23077
rs142245813	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77219055	TAGATAGTGGTAATA[C/T]TCACTTAAGCTATGA	23077
rs142246436	snp	C/T	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77221638	CATCTTATCTAACTG[C/T]AATGCACCTTTCCCA	23077
rs142270230	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77316756	TTTCTGTTGGTCCAG[A/G]TGGCTGACTTCATGG	23077
rs142271901	snp	A/G	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77134061	AAATATTTACTAAAT[A/G]AGCAATTAATGAATT	23077
rs142294005	snp	C/T	0.000703026	0.0187355	intron-variant	MYCBP2	GRCh38.p7	13:77273462	CTAAGCAGATATAAA[C/T]ATGAAATACCTGAAT	23077
rs142342966	snp	C/T	0.000329451	0.0128303	missense	MYCBP2	GRCh38.p7	13:77251224	AGTCTCCACAGACAG[C/T]GCAAACCATGCACTG	23077
rs142388586	snp	A/G	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77174028	TGAAATTGCAGACCA[A/G]AAATTATAGAGTGAC	23077
rs142402567	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77214977	TATAAAATAGTGTGT[C/T]TGCATGCTTATATAT	23077
rs142448637	snp	G/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77299934	AGCTACACTGCTTAA[G/T]AAAAATCAAATACTT	23077
rs142457195	snp	C/T	0.00953873	0.0683987	intron-variant	MYCBP2	GRCh38.p7	13:77130845	AAGTAACATGAAAGG[C/T]AATTGTTAAAAGTAA	23077
rs142463744	snp	C/T	0.00874735	0.0655527	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081762	GGATCAAATTGATTA[C/T]GAATAACTTACAGTT	23077
rs142478549	snp	C/T	0.00478085	0.0486577	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77082225	GACCCATTTTAAATA[C/T]AAAAGAATTAGACAG	23077
rs142482599	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77171087	ATTCCAATGGAAAAA[C/T]TCATAGAGCTGAATT	23077
rs142509768	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77296372	GACTCCAGCCTGGGT[A/G]ACAAAACAAGACCCT	23077
rs142514250	in-del	-/GAC			intron-variant	MYCBP2	GRCh38.p7	13:77316142	GAGATCAGAAAGAAA[-/GAC]AATATGATTATTTAC	23077
rs142529798	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77152345	TCAACTCAAACACAT[A/G]TGCCAGCATAAAAAG	23077
rs142553020	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77294458	TTAAAAAGAAGATAT[A/G]GAAATACTGAGAGCA	23077
rs142563735	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075800	TCAATTGACTTAACA[G/T]GTAGTTACACAGTCT	23077
rs142564223	snp	A/C	0.0256215	0.110247	intron-variant	MYCBP2	GRCh38.p7	13:77299657	GAATATAAAAGAGAA[A/C]CTCTAAAAACCAGTC	23077
rs142565851	snp	A/G	0.0174175	0.0916809	intron-variant	MYCBP2	GRCh38.p7	13:77239293	AGTATAATTATTAAC[A/G]TACTACTAAATTTTT	23077
rs142567657	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77166050	ATTTGGACCCAACTA[C/T]ACAGACAGCTAGCTA	23077
rs142592449	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77181156	TCAAGAAGTCACAGA[A/G]TCTCAATAAAGGAAA	23077
rs142601380	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77292318	AGCCATGAGTATAAA[C/T]TGCTTGTGAGATTTA	23077
rs142602360	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77152764	GAGAGCCACTTCCAC[C/T]GTTTGATAAAATCCG	23077
rs142620503	snp	C/T	0.000148619	0.00861902	missense	MYCBP2	GRCh38.p7	13:77093294	TCATCCTGGAATAGA[C/T]TGTCATCTTGATAGC	23077
rs142637287	snp	A/C/G	0.00189586	0.03073	intron-variant	MYCBP2	GRCh38.p7	13:77233119	GTGGAAGAAATTGGG[A/C/G]AAGTATCCCACCTAG	23077
rs142641439	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77321504	AAAACCATCAAGGGT[A/G]ATCAGTGTCTACTGA	23077
rs142651122	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77294968	ATGATGCAGGTAAAC[C/T]GAAAATCCTACCCAA	23077
rs142662799	in-del	-/ATAAA			intron-variant	MYCBP2	GRCh38.p7	13:77267392	TGAAACCCCTTTAAC[-/ATAAA]ATAAAATAAAATAAA	23077
rs142664502	snp	C/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77108636	CTGAGAAAGAGACAA[C/T]GCTTACGCAGCACAA	23077
rs142670993	snp	A/C/T	0.00557542	0.0525036	intron-variant	MYCBP2	GRCh38.p7	13:77254442	TAATATTTCAATATG[A/C/T]TCTGTACTTTCCTGG	23077
rs142671800	snp	A/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77310308	TGTTTTGCACTTCTT[A/T]GATTCCCTGAATTCA	23077
rs142719870	snp	A/C	0.00716266	0.059414	intron-variant	MYCBP2	GRCh38.p7	13:77306640	TCATGCATATTTGTA[A/C]TCTTAAGTAAACATA	23077
rs142753608	snp	C/G	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77268417	GTGGCAAATAAAAAT[C/G]TGATGAGATATTTTA	23077
rs142757927	snp	C/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77304061	AACCATTGTGGAAAA[C/T]AGAATGGAGGCTCCT	23077
rs142782752	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77054369	CTACCGTATTATAAG[C/T]AGAAGAGTGATCCAG	23077
rs142783857	snp	C/G	8.23879e-05	0.00641772	synonymous-codon	MYCBP2	GRCh38.p7	13:77066037	GATCTCTGAGATCTG[C/G]GTAGGGGTTGAGCCC	23077
rs142790976	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77173730	GCTACAAGAAAAATT[C/G]AGACTCAGTGAGAAA	23077
rs142802398	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77200070	GAGCTGAGAGAAGAA[A/G]GCTTCAGATGATCAA	23077
rs142807127	snp	A/C/T	0.00219226	0.0330356	missense	MYCBP2	GRCh38.p7	13:77098632	TGTGGTGAGGAGGAG[A/C/T]GTGGAGAACTAGCAC	23077
rs142825478	snp	G/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77068922	AAAAGAATAAGACAA[G/T]AATGTAAATTGATAC	23077
rs142832510	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77058026	TGTATTTTTGTAGTA[A/G]AGACGGGGTCTCACT	23077
rs142832927	snp	A/C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77158861	TGGGTGGAAGCCTGA[A/C/T]TGTGGCAGCACACAC	23077
rs142838697	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77317209	CACTCATCTCGGCCT[C/T]CCAAAGTGCTGGGAT	23077
rs142855337	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77117968	TTGTCATACATTTCA[C/T]AGATACCAAATTCAC	23077
rs142862318	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77208760	TACAGAGTATGACCA[C/T]CCTTTTTCCTGTATG	23077
rs142862648	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77154981	TGTATATATAAAGTA[C/T]ATTATATGTACTTAA	23077
rs142887854	snp	C/G/T	0.000978506	0.0220977	synonymous-codon	MYCBP2	GRCh38.p7	13:77181815	TACTTCTCCATCATA[C/G/T]GCAATCGGGAAGATG	23077
rs142899707	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77063785	GAAAAAGAAATAATG[C/T]ATGCAAGGAGGAAGG	23077
rs142900411	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77263844	AGAGGTCGTTCAAGG[C/T]TCTACAGTCTATCTA	23077
rs142906868	snp	C/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77259992	CTACAATGTGCCAGA[C/T]ACTGTGCTGGGCACT	23077
rs142925528	snp	A/G	1.64838e-05	0.00287083	missense, intron-variant	MYCBP2	GRCh38.p7	13:77233215	CTGAGTCTGGCTAGA[A/G]CCTGTTCTCGATGGT	23077
rs142951653	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77225174	TAAAGGATTATTTCA[C/T]CTTCCAGACTGTCTT	23077
rs142974804	snp	C/T	1.6537e-05	0.00287545	missense	MYCBP2	GRCh38.p7	13:77051884	TCTCCCCGTCCAGCC[C/T]CAGCATCGCAGCGAG	23077
rs142979925	snp	C/T	0.00438332	0.0466095	intron-variant	MYCBP2	GRCh38.p7	13:77127364	AATGCTGTGATAAAA[C/T]TGTTTCCTATGTGAA	23077
rs142999420	snp	C/T	0.00478085	0.0486577	intron-variant	MYCBP2	GRCh38.p7	13:77311495	TATAAATATGCTACA[C/T]TGAGGAAAGACAAGG	23077
rs143010585	snp	A/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77271178	TAATTTCAATATCTA[A/T]GGACTTGGCAGGATT	23077
rs143022675	snp	C/T	0.00795532	0.062565	intron-variant	MYCBP2	GRCh38.p7	13:77055915	ATTTGAAAAACATTC[C/T]GTAAATTCTTTAGAA	23077
rs143029082	snp	A/G	0.0126979	0.078662	intron-variant	MYCBP2	GRCh38.p7	13:77317894	GTCAGCTGAGATCAC[A/G]CCATTGCACTCCAGC	23077
rs143036573	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77237266	TGTGTTCTTCTTGTA[C/T]TGTAAAATGAGAAAA	23077
rs143042145	snp	C/T	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77104253	AAAAAGTGCTGTTTT[C/T]GGCTGATTCATTATT	23077
rs143050819	in-del	-/G	0.00953873	0.0683987	intron-variant	MYCBP2	GRCh38.p7	13:77121965	ACTGTTCTAAGTTAT[-/G]AATGTGAAAATTATG	23077
rs143069733	snp	A/T	0.00094373	0.0217019	synonymous-codon	MYCBP2	GRCh38.p7	13:77263992	AATATTTTGACCTTC[A/T]GTGTGGCAATCTGTG	23077
rs143120354	snp	A/G	0.0256215	0.110247	intron-variant	MYCBP2	GRCh38.p7	13:77234358	TTTTCATGATTCTCT[A/G]TTGATCTTCAGTTTA	23077
rs143120621	snp	C/G	0.0283406	0.115616	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77292958	AGCAAGACTCCGTCT[C/G]AAAAAAAAAAAAAAA	23077
rs143124998	in-del	-/AC	0.991952	0.0256364	intron-variant	MYCBP2	GRCh38.p7	13:77070574	CAGACAAACAAACAA[-/AC]ACACACACACACACA	23077
rs143197906	snp	C/T	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77129090	CAAAGGTTTTAAAGA[C/T]ACAAAATTTGTTATA	23077
rs143197944	snp	C/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77147502	ATGTCCAACTGCTCA[C/T]CTACTTCTAACTCCT	23077
rs143232862	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77056187	AGGGGAAGGCAGAAC[A/G]CCAGGTGACAGAAGT	23077
rs143239823	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291066	GGATTGGAAAATTCA[A/G]TATCATTAAAATGGC	23077
rs143250859	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77073479	TTTCAAGATCCAGAA[C/T]AAGTCAGAGCTATCT	23077
rs143271961	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77052847	TAAGAAGAAAAGGCC[A/G]GCTGGGCATGGTGGC	23077
rs143277437	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77212659	AAATATGTAATGTTG[C/T]TTTCACATGATATGT	23077
rs143288023	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77143315	TTCAATGTGGACAGG[C/T]GCTGTCCAATCAGCT	23077
rs143297755	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77121775	GATACATTACTGAAT[A/G]CATACTAATATTTCT	23077
rs143312842	snp	A/C	1.68838e-05	0.00290544	missense, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087549	CTGGTTCCACTGGTG[A/C]AGGAGTCAGTGATGC	23077
rs143321266	snp	C/T	0.0260105	0.111035	intron-variant	MYCBP2	GRCh38.p7	13:77142906	CAAAATCAGAAAAAG[C/T]CCAAAATCTAGAATA	23077
rs143328241	snp	A/C/T	0.000197737	0.00994142	missense	MYCBP2	GRCh38.p7	13:77174446	TCTCCATTGGCTGTA[A/C/T]GGCTTCCATAGTTCC	23077
rs143342012	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77284504	ATGGCTGCCAAAAAA[C/T]ATCACCTGAAAGTTT	23077
rs143350113	snp	C/G	1.65441e-05	0.00287607	missense	MYCBP2	GRCh38.p7	13:77097857	GGGTGCAATATTAAA[C/G]ATATTCAGTGCAGAT	23077
rs143351131	in-del	-/G	0.0376037	0.131863	intron-variant	MYCBP2	GRCh38.p7	13:77248798	AAACAGGGTCTCAAA[-/G]AGCTCCTTGTACACT	23077
rs143363601	snp	A/G	1.68207e-05	0.00290001	missense	MYCBP2	GRCh38.p7	13:77097577	ACTCTTTCTTTTTAA[A/G]AACTGCACAGGAACC	23077
rs143369248	snp	A/G	0.00993419	0.0697739	intron-variant	MYCBP2	GRCh38.p7	13:77103075	ACTCAAACATATATA[A/G]ATGTAAATAAAATGA	23077
rs143371754	in-del	-/CCCCC			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77293738	AGAAAACTCAACCAA[-/CCCCC]CCGCCACTGGCTTTG	23077
rs143379789	snp	C/T	1.64781e-05	0.00287033	synonymous-codon	MYCBP2	GRCh38.p7	13:77139229	ACTCTTGCCAAGATG[C/T]TGATTAAAAGAGAGG	23077
rs143404195	snp	A/C/G	0.00716266	0.059414	intron-variant	MYCBP2	GRCh38.p7	13:77207975	CCACCCGCCCCAGCC[A/C/G]CAGATGAATGAGTAT	23077
rs143409725	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77119088	AATATTTTGCTTAGA[G/T]GAATAATTTAAAAAT	23077
rs143410657	snp	A/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77099815	AAAAGAAGAATCACC[A/T]CCCTTTTCTAAGGCA	23077
rs143411857	snp	C/T	0.0267878	0.112589	intron-variant	MYCBP2	GRCh38.p7	13:77210337	AGCTGGGATTACAGG[C/T]GCCCGCCACCACGCC	23077
rs143420440	snp	A/C/G/T	0.00152814	0.0276002	missense	MYCBP2	GRCh38.p7	13:77206787	GCATCAGCAACCACC[A/C/G/T]CATTGTAACACCACA	23077
rs143427584	snp	G/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77223614	ATTTAAGAAGCTGAT[G/T]AGGCAGTTCATGGTG	23077
rs143444094	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77100278	AGTGTGTATAGTCAC[A/G]CTCTATTTCTCTATG	23077
rs143501376	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77151349	ATTTTAAAGCACTAA[C/T]GTCAGTTTGAGCTGC	23077
rs143508394	snp	C/T	0.0372196	0.131242	intron-variant	MYCBP2	GRCh38.p7	13:77238115	CGGTGTGGTGGTGAA[C/T]GCCTGCAGTCCCAGC	23077
rs143544881	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77256996	TAAGTGTCCATCAAC[A/T]GATGAGTGGATAAAG	23077
rs143546875	snp	C/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77311830	TTTGTAAGGTCAGAA[C/G]AAAGACACAATGGTA	23077
rs143594658	snp	C/T	4.94425e-05	0.0049718	missense	MYCBP2	GRCh38.p7	13:77066014	ATATCCTTGATAAGT[C/T]TAATGATGATCTCTG	23077
rs143606038	snp	C/G	0.0217236	0.101931	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77078075	AATAGACATTAAGTT[C/G]ATATTATTTTAATTA	23077
rs143610810	snp	A/G	0.00438332	0.0466095	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77083883	CCACTGGCAATTTCT[A/G]TTACCAGTTTCTTGG	23077
rs143639527	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77308371	TCCTTCAGCCTGCTA[C/T]GTCAAGATAGGTTAA	23077
rs143656557	snp	C/T	0.00636936	0.0560724	intron-variant	MYCBP2	GRCh38.p7	13:77239483	AGTGACTCAGATCTA[C/T]TTCCAAGACCCTTGA	23077
rs143700322	snp	C/T	0.00676609	0.0577691	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77074423	CATACATAAAAATCA[C/T]GAATCAAAAAAACAA	23077
rs143701774	snp	A/G	8.24994e-05	0.00642206	synonymous-codon, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081900	TTCACTATCGCCATC[A/G]TCTGACTTTGACAAA	23077
rs143702720	snp	A/G	0.0349115	0.127424	intron-variant	MYCBP2	GRCh38.p7	13:77295399	GGCCTCCCAAAGTGC[A/G]GGGATTACAGGCGTG	23077
rs143702848	snp	C/T	0.0115144	0.0749975	intron-variant	MYCBP2	GRCh38.p7	13:77054896	GTGAGCCACTGTGCC[C/T]GGCCAAGATTGATGA	23077
rs143710456	snp	C/T	0.0127008	0.0786707	utr-variant-3-prime	MYCBP2	GRCh38.p7	13:77045336	CATCCTCTTGGGGGA[C/T]GAAGGCAATTTTTCT	23077
rs143733643	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77123148	ATCTTTGTACTTCCA[C/T]ATTAAATATTATCAC	23077
rs143766994	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77323358	GTAATTAATTCATTT[C/G]ACATTGACTGATAAC	23077
rs143783438	snp	C/T	0.0134861	0.0810011	intron-variant	MYCBP2	GRCh38.p7	13:77110432	AACCCTGTTTTCTGT[C/T]AAGATGTTTATCAAG	23077
rs143786765	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77125030	TAGAAGGGATAGAAC[A/G]TTCAGTCCTGGACTG	23077
rs143804920	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77250484	AAAGCTGATCACACA[A/G]AGAATATCCCATCAT	23077
rs143826033	snp	C/T	0.00478085	0.0486577	intron-variant	MYCBP2	GRCh38.p7	13:77173074	TCCAAATGAAGATGT[C/T]AGAAGAGAGACCCGG	23077
rs143827073	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77143854	GGTAACTGTAACACA[A/G]TGGTAAGGATTTGCA	23077
rs143830500	snp	C/T	0.00795532	0.062565	intron-variant	MYCBP2	GRCh38.p7	13:77232042	TATTTCTGCAGAGTA[C/T]ATCTTAAGTTGTGCT	23077
rs143830725	snp	A/C	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77162984	TATGCAAAAATGGGA[A/C]CTTCTTCTGCAACTT	23077
rs143831208	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77120262	TCTAGCTTAAGTTAA[G/T]GGAAATCAGGTACCC	23077
rs143838484	snp	C/T	0.000153988	0.00877328	missense, intron-variant	MYCBP2	GRCh38.p7	13:77233224	GCTAGAGCCTGTTCT[C/T]GATGGTTCATAAAAA	23077
rs143907596	snp	A/G	0.0146672	0.084371	intron-variant	MYCBP2	GRCh38.p7	13:77119232	AGATAATGAAATTAT[A/G]TGATGGATAATAACT	23077
rs143918923	snp	C/T	0.00478085	0.0486577	intron-variant	MYCBP2	GRCh38.p7	13:77170288	AAGAAAAGCACTTTG[C/T]TGATTAACATTTTAG	23077
rs143923006	snp	A/C	0.0142736	0.0832652	intron-variant	MYCBP2	GRCh38.p7	13:77264480	AATGGATATTCAAAA[A/C]CAGTTGTACATTTCC	23077
rs143929151	in-del	-/T	0.0368353	0.130617	intron-variant	MYCBP2	GRCh38.p7	13:77320569	GCTAAAAGCATTAGG[-/T]TAAAAGGCATTCACA	23077
rs143948094	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77262336	TAATCTGTTTCTCTT[A/G]TTCCAAACCAGTACC	23077
rs143950298	snp	C/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77297762	ATGTTATCCTTGACA[C/T]TGCCTTCAGTTTCAC	23077
rs143960871	snp	A/G	0.0217236	0.101931	intron-variant	MYCBP2	GRCh38.p7	13:77048556	TCTAAATGAATGGAT[A/G]AGTTAGAGGGATGTG	23077
rs143967767	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77282702	GCCCTACATAGCACA[C/T]ACTGGATACTTCACA	23077
rs143968169	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77310609	TCAAACAGTATCATA[C/T]ATATATAATTGGATT	23077
rs143968936	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77101115	GACAGCTGGAGACAT[A/G]TTTATCACCTTTATC	23077
rs143988183	snp	C/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77063863	ACTGTCAAAAATACC[C/T]ATTTCAGGTGTCACA	23077
rs143989652	snp	A/C	0.00199481	0.0315187	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77327926	TGTCTATAAAAAAGT[A/C]ACATTTGCTCAGTCC	23077
rs144042363	snp	C/G	0.0422008	0.138995	intron-variant	MYCBP2	GRCh38.p7	13:77200340	GAAGGGAAGTTTAGA[C/G]AAAAAAGAATAAAAA	23077
rs144059496	in-del	-/A/AA			intron-variant	MYCBP2	GRCh38.p7	13:77248154	CTTAAAGTATAATCA[-/A/AA]AAAAAAAAAAAAGAA	23077
rs144077319	snp	C/G	0.00478085	0.0486577	intron-variant	MYCBP2	GRCh38.p7	13:77112827	CAACTGAATTACTCT[C/G]ATTAGAAAACAACCT	23077
rs144088780	snp	C/T	0.0637235	0.166737	intron-variant	MYCBP2	GRCh38.p7	13:77058939	GCAGTGAGCCGAGAT[C/T]GTGCCACTGTACTCC	23077
rs144091852	snp	G/T	0.00835141	0.0640778	intron-variant	MYCBP2	GRCh38.p7	13:77150412	CTCCCAAAGCCCTGG[G/T]ATTATAGGTGTGGGC	23077
rs144096472	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77147934	GAATGGTATTCCATA[C/T]CTGCTCTAAACCTAG	23077
rs144104931	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77236522	ATTTTTAAAGGATTT[C/T]ACCTCAAAGGTGTTT	23077
rs144111490	snp	A/C	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77196977	GAAGATGATGAGCAA[A/C]CAGCAGGAGACTAAG	23077
rs144132500	snp	A/C	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77253577	ATTTATGGTAATTAA[A/C]TGAAGGGCAGAGAGG	23077
rs144134869	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77055097	TAAGTAGGCAAGAAT[A/G]GAGCTCTAGGAAAAC	23077
rs144137984	snp	C/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77286126	AGAAGAACCTGACAA[C/T]ATGATTAAGGATGGT	23077
rs144163347	in-del	-/ACAC			intron-variant	MYCBP2	GRCh38.p7	13:77245745	CCAGAACGTAAAGTA[-/ACAC]ACACACACACACACA	23077
rs144180857	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77212243	GAGGCAGTAGATAAA[A/G]ATCAATCTATGAAAC	23077
rs144183951	in-del	-/AC/CC			intron-variant	MYCBP2	GRCh38.p7	13:77216993	GTGTGAGAAAGAGAA[-/AC/CC]CAGCCACATGTGCAA	23077
rs144188721	snp	C/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77109549	GATATTGTTAATTAC[C/T]GGCCTGGCAAAAGTT	23077
rs144209096	snp	A/G	6.59011e-05	0.00573988	missense	MYCBP2	GRCh38.p7	13:77243095	GCCTTCTGATTACAC[A/G]TTGCCGTTTTTCTTC	23077
rs144228579	snp	C/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77161512	TACCAACCTCACCTT[C/T]TGCTGCTTCTTATAA	23077
rs144242210	snp	C/G	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77319623	CAAAAGCCATCTGAT[C/G]ATTGTCCTCATAATT	23077
rs144244516	snp	G/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77247470	GTTCATGGATTAGAA[G/T]ACTTAATGTTTTTAA	23077
rs144281411	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77200071	AGCTGAGAGAAGAAG[C/G]CTTCAGATGATCAAA	23077
rs144283320	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77303368	CCATGATTAATCAAC[C/T]TGACCTAATTGGCAT	23077
rs144362722	snp	C/G	0.0174175	0.0916809	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228498	GGTGATAGAGTGAGA[C/G]CCTGTCTCAAAAAAA	23077
rs144373860	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77317661	AAGTGGGTCCCGGCC[A/G]GGCGCGGTGGCTCAC	23077
rs144377809	snp	A/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77133707	CTCTGCTTTACCTAT[A/T]TCAACTATTCATTAG	23077
rs144400361	snp	C/T	1.64776e-05	0.00287028	missense	MYCBP2	GRCh38.p7	13:77068717	AGGCATCAGAGGAGG[C/T]ATCTTCATCATTTGG	23077
rs144404634	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77273161	TACTAAAAAACTCAG[C/G]GAAAGATGGGAAGAA	23077
rs144409085	snp	C/G	1.66896e-05	0.00288869	missense, utr-variant-5-prime	MYCBP2	GRCh38.p7	13:77288364	TGATTACTGTATTCT[C/G]TAAGTTTTCAGACTG	23077
rs144436188	snp	A/G	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77221366	AAGTAATGTTTTTAG[A/G]TAATCTCTTCATTTT	23077
rs144464392	snp	A/G	0.0182019	0.0936463	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075193	ATCCTGGATGACAGA[A/G]AGAGACCCGGTCTCA	23077
rs144465482	snp	C/T	0.000153988	0.00877328	synonymous-codon	MYCBP2	GRCh38.p7	13:77121404	TCCATAATCAAATCC[C/T]TGGGCACTGCAACTT	23077
rs144474570	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076048	CTAGTCAGAGTTGAC[G/T]TCTCTTTTTGCAAAT	23077
rs144484713	snp	C/T	5.02138e-05	0.00501043	missense	MYCBP2	GRCh38.p7	13:77191695	CATCATCTGTGGTAA[C/T]AGATGCCTGTCCATG	23077
rs144485377	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77124185	CTGCTATGTCACCAG[C/T]TGTACAACCATAGAC	23077
rs144488320	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77214109	AGCACCAACTAAAGG[C/T]AAAGGAACTTGGAAG	23077
rs144508071	snp	C/T	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77091511	AGATGACATCTTTAA[C/T]TGAATGGCTACCCTG	23077
rs144509920	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77301420	AGAGCAAGACTCCAT[C/T]TCAAAAAAAAAAAAA	23077
rs144520983	snp	A/C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77113560	GTAGCAAACAAAGAG[A/C/G]TGGGGGAAGAGGGAG	23077
rs144530761	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77217000	GAAAGAGAACAGCCA[C/T]ATGTGCAATAATAAA	23077
rs144565262	snp	A/G	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77069450	ATATGGTGAAATCCC[A/G]TCTCTACTAAAAATA	23077
rs144565671	snp	G/T	0.00835141	0.0640778	intron-variant	MYCBP2	GRCh38.p7	13:77146461	CAGATAACATCTTTT[G/T]AGTACATTAAAATTT	23077
rs144565711	snp	A/G	0.000346452	0.013157	synonymous-codon	MYCBP2	GRCh38.p7	13:77161924	CAATGCAGCCTCCTC[A/G]AGAATTTCAAGGTCT	23077
rs144590133	snp	A/G	3.29462e-05	0.00405857	synonymous-codon	MYCBP2	GRCh38.p7	13:77150830	CCCTCCATAAGTCAT[A/G]TCAGTATTAGAAGAT	23077
rs144591787	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77209659	AAAGACCACTCACCC[A/G]TAGTCTCTTGTTATT	23077
rs144601872	snp	C/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77089594	ATTCTTGAGGTAGAA[C/T]CCCCAGCTCCAATTT	23077
rs144602473	snp	A/G	0.0103295	0.0711199	intron-variant	MYCBP2	GRCh38.p7	13:77301380	AAGAGCCAAGATCGC[A/G]CCACTGCACTCCAGC	23077
rs144622707	snp	A/G	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77142448	ATCTGAGTCTATATA[A/G]TTACATTAATGTATG	23077
rs144624584	snp	A/C/T	0.000131829	0.0081178	missense	MYCBP2	GRCh38.p7	13:77171561	TTACAACAGACAATG[A/C/T]TCTGCTACAGTTTTT	23077
rs144627155	snp	C/T	0.00102155	0.0225772	missense	MYCBP2	GRCh38.p7	13:77177822	AACCAACCACAACTA[C/T]TCCAGGTTTGTCTAC	23077
rs144629115	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77230612	AATTACTCACATAGC[C/T]GAAAGATAATTTTAT	23077
rs144652087	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77102340	TTTATACTGTCAATT[A/G]TATAATGAGAAACAT	23077
rs144652744	snp	C/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77180524	CGTATCAAAGTACCA[C/T]ACATTTACGAAATGT	23077
rs144657404	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77223779	ACAAATGGAAAGGTA[C/T]ACCCTTTCCCTTTAA	23077
rs144662591	in-del	-/AC			intron-variant	MYCBP2	GRCh38.p7	13:77274281	AGTGGTGAAGATGAA[-/AC]ACACACACACACAAA	23077
rs144664478	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77227471	AAAAGCCTACACACA[C/T]ACACACACATACACA	23077
rs144691865	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77093818	TGGGTAGGAACATAC[A/C]TAAGATCATATTTGA	23077
rs144698035	snp	A/C	0.0182019	0.0936463	intron-variant	MYCBP2	GRCh38.p7	13:77320769	AGCGCCATATACAAT[A/C]TTCTTGCTAAAAAAT	23077
rs144699563	snp	A/G	0.0275645	0.114116	intron-variant	MYCBP2	GRCh38.p7	13:77154417	AGGGAAGAAGAGAGG[A/G]AAAAAAAAAGCAGAT	23077
rs144702217	in-del	-/GT			intron-variant	MYCBP2	GRCh38.p7	13:77319110	GTGCAGTTTGGGAAC[-/GT]GTGTGTGTGTGTGTT	23077
rs144729494	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087169	CAGAGTGACTGGGAA[A/T]AAGATAAATGTCACC	23077
rs144737618	snp	C/T	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77174245	AGTTAGCAATTTTAC[C/T]TGGTAGTAGACTGTG	23077
rs144747705	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77232789	AAGCATATAAACAGC[A/G]TTCAAAAAAGAATTG	23077
rs144749229	snp	C/G/T	0.00993419	0.0697739	intron-variant	MYCBP2	GRCh38.p7	13:77301081	TTCCCAGTGGTATAT[C/G/T]TCCTCAGAAATGTAA	23077
rs144761855	snp	C/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77096171	AGTACAAATATTAAA[C/T]TTGTATATGATTTCC	23077
rs144762909	snp	C/G/T	3.30421e-05	0.0040645	synonymous-codon, missense	MYCBP2	GRCh38.p7	13:77051817	TCTGCCTACCTGAGC[C/G/T]CTGGAAACATCAGAA	23077
rs144780646	snp	A/G	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77249505	TAATTTATAGATTTT[A/G]TTCACGATATATACT	23077
rs144829532	snp	A/G	0.0271762	0.113356	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77086269	ACTGACAGCCTTTTA[A/G]ACAAACTCAGTATTT	23077
rs144830142	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77173268	GTATTTTGTATAAGA[C/T]ATAAAGTTTGGATGG	23077
rs144855892	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77316766	TCCAGGTGGCTGACT[C/T]CATGGGGTGGTCACT	23077
rs144862453	snp	G/T	8.26562e-05	0.00642816	synonymous-codon	MYCBP2	GRCh38.p7	13:77095590	GCATTGGTTTTCTCC[G/T]AGATTGTTTGACCTG	23077
rs144875480	snp	C/T	0.00755907	0.0610114	intron-variant	MYCBP2	GRCh38.p7	13:77103729	TCATGGCTTAACCTA[C/T]TGTCACTTGGTTTCC	23077
rs144890507	snp	C/T	8.4139e-05	0.00648555	missense	MYCBP2	GRCh38.p7	13:77261373	TTTGCCAGTGTAATA[C/T]ATCTTATGTATTAAA	23077
rs144898759	snp	C/T	0.00478085	0.0486577	intron-variant	MYCBP2	GRCh38.p7	13:77242722	AGTCCGGGTGAAGGA[C/T]AAGTTGTGAGAATAT	23077
rs144934192	snp	C/T	6.59761e-05	0.00574314	missense	MYCBP2	GRCh38.p7	13:77066077	CAATGACTTTCACCT[C/T]GTCGGAGATAACTAC	23077
rs144941816	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77111013	ATGATAAGGATGAGA[A/C]GTCTGATTACAAAAA	23077
rs144978250	snp	A/G	3.31719e-05	0.00407245	synonymous-codon	MYCBP2	GRCh38.p7	13:77098973	TGATTTTCCTGATGT[A/G]GAGGCTGGTTTAGAA	23077
rs145007183	in-del	-/A	0.0667028	0.170006	intron-variant	MYCBP2	GRCh38.p7	13:77096937	TCATTACATTTACTG[-/A]AAAATGCAGTCTTCT	23077
rs145009274	snp	A/G	0.0103295	0.0711199	intron-variant	MYCBP2	GRCh38.p7	13:77065890	AATAGTCTTTAAGTA[A/G]AGTTACACTAATCTA	23077
rs145021130	snp	A/C/G/T	0.000184581	0.00960532	missense, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081634	TAAGTCCTTTAAGCA[A/C/G/T]ATTACTATGCATAAT	23077
rs145024098	snp	C/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77163191	CCACCCTTCAACATA[C/T]ACTTTTTGAGTATTT	23077
rs145047601	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77304564	ACTATCATAAACAAC[A/G]ATGTATTATACAACT	23077
rs145047716	snp	C/T	0.0189856	0.0955633	intron-variant	MYCBP2	GRCh38.p7	13:77245286	TTATAAATCATCCTA[C/T]TACAAAGACACATGT	23077
rs145055995	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77199996	GCAACTCTCCTCCTC[A/C]AAAGAAACACAGTTC	23077
rs145067678	in-del	-/ATG	0.00874735	0.0655527	intron-variant	MYCBP2	GRCh38.p7	13:77059959	AATACCATAAAAAAT[-/ATG]ATAACCAAAAATTAA	23077
rs145092128	snp	A/G	0.000181454	0.00952334	synonymous-codon, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081559	GGTTTCTGTGGAGCC[A/G]TCTGTCAAACTGCCA	23077
rs145095322	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77318470	TTAAAAACTACAAAT[A/G]CTGGGCCAGGCGCAG	23077
rs145100956	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77114521	TACTTTAGTGTGTTC[A/G]TATTCTCAAATGTAA	23077
rs145126830	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77229937	ATCTCTAGAACAATT[C/G]AGATGTTCCTAACTA	23077
rs145140124	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77110022	GTAAAACATGTGTGT[C/T]TGAACAACATGAAAT	23077
rs145152361	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77255327	TTACTTTACTCATCT[C/G]CTTTCTAATTCATTA	23077
rs145156333	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77198542	ATTCAGGCAGAAACT[A/G]TAGTTTTCTCTTTCA	23077
rs145172182	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77116434	TTACCTTTCCCAACA[C/T]GGTATAAAAAATACA	23077
rs145190849	snp	C/T	0.0115144	0.0749975	intron-variant	MYCBP2	GRCh38.p7	13:77136208	TAACTTCTTAGTTCC[C/T]AGACTTAGGCACTTG	23077
rs145190951	snp	A/G	0.0368353	0.130617	intron-variant	MYCBP2	GRCh38.p7	13:77187944	GGCGTGGTGGCAGGC[A/G]CCTGTAATCCCAGCT	23077
rs145194377	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77274324	CAGCAGAGGTCTCTG[C/T]ACAAAATTCCCTGAA	23077
rs145194677	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77121638	ATCAATTTAAATACC[A/C]GTCAGGTCATCTTAA	23077
rs145213353	snp	A/G	0.000132433	0.00813627	synonymous-codon	MYCBP2	GRCh38.p7	13:77140137	GATGCGAAGCCCCGC[A/G]CTGTCCTTGGCCACA	23077
rs145222136	snp	A/G	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77265638	ATGGTATTCATTACC[A/G]TCTATAAACCTGACA	23077
rs145236140	in-del	-/AG	0.0948562	0.196037	intron-variant	MYCBP2	GRCh38.p7	13:77124801	CCACCAAGATATCAA[-/AG]AGAGGGGGACAAAAA	23077
rs145241279	snp	A/G	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77047912	GGGCCCCAGCCTCAC[A/G]GGAGCATCCTGTTTG	23077
rs145241559	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77170990	ATTAACCCTATATTA[A/C]AAAATGAAATGTACT	23077
rs145245218	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77276994	AGATAAGACTAAAGC[A/G]CATATTATATGCCAA	23077
rs145259609	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77049948	GCCTAATTTACTTTT[C/T]TCATCTGATGCTATC	23077
rs145281513	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77312471	GGAGAATAAAAGGAT[C/G]TGTAGGGTTGCAAGG	23077
rs145284771	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77182725	GGATGCAAAGTTGCC[A/T]GGGATGCATTAGTGA	23077
rs145299813	snp	C/T	0.00676609	0.0577691	intron-variant	MYCBP2	GRCh38.p7	13:77070268	ATAAAAGGGCGAGCA[C/T]AAAAAAGCCTTCATA	23077
rs145313509	snp	C/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77066677	ATATTTAAAATATAG[C/T]TAGATATTATAAACA	23077
rs145324155	snp	A/G			upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77328391	AAGACATGTGGAATC[A/G]TAGTATTTTAGTACT	23077
rs145332191	snp	A/G	0.0146672	0.084371	intron-variant	MYCBP2	GRCh38.p7	13:77322869	CCAACAGAATGTTCC[A/G]ATTTTGATTGGCCTC	23077
rs145332823	snp	C/T	0.000148649	0.00861987	missense	MYCBP2	GRCh38.p7	13:77185936	CAGGTACCCACAAAG[C/T]GCAGTCTCTCTAAAT	23077
rs145345667	snp	C/T	0.00953873	0.0683987	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77086376	TGGCTGCTTAAAAGA[C/T]CTCTTTCTTTGTTTT	23077
rs145353505	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77115436	TTTTTCATGTCTCTG[C/T]GTGCACACACATAAG	23077
rs145356573	snp	A/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77206131	AGCAACAAAATACAT[A/T]GTTACATAGAGTGAT	23077
rs145372801	snp	C/T	1.64741e-05	0.00286998	synonymous-codon	MYCBP2	GRCh38.p7	13:77174376	ACTGCTCAAGCTGCA[C/T]GTGCTGAATGTGAAT	23077
rs145377950	snp	C/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77140223	TAGAGATCTTACAAG[C/T]AGCAAGAAGTAAAAT	23077
rs145382394	snp	A/T	0.00874735	0.0655527	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228055	ATTAAAATATATATT[A/T]TATATATATATCTGT	23077
rs145406662	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77256556	CTCAAATCCAATTAA[A/C]AAATGTGAAAAAGTT	23077
rs145417376	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77252192	CAGGGATTCCTTCAC[A/G]GCAAGAAATCAGCAA	23077
rs145438156	snp	C/T	0.00676609	0.0577691	intron-variant	MYCBP2	GRCh38.p7	13:77060777	CAACCTTATAATAAA[C/T]AGAGATCTTAGTGAT	23077
rs145445811	snp	C/G	0.00478085	0.0486577	intron-variant	MYCBP2	GRCh38.p7	13:77151446	ATCTTATACCTAAAG[C/G]CCAAATATGTTTCTT	23077
rs145466513	snp	C/G	0.0150606	0.0854603	intron-variant	MYCBP2	GRCh38.p7	13:77197281	TACAGAGACTATCTA[C/G]GTGGCTAGTCCAAGA	23077
rs145470432	snp	A/G	0.0111196	0.0737302	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77293205	CTGTAAGAAAGTGAA[A/G]TCATGTGCTGGAAGG	23077
rs145473285	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77222549	AGCTCGAAGGGTAGA[C/G]AGTGGTTCTCATCCT	23077
rs145498722	in-del	-/ATAAAG	0.0614824	0.164198	intron-variant	MYCBP2	GRCh38.p7	13:77122011	AACTTATTTTATCAC[-/ATAAAG]ATATTTTTCCCAAAT	23077
rs145501788	snp	A/C	0.0111196	0.0737302	intron-variant	MYCBP2	GRCh38.p7	13:77205732	CTTTAAACATCATTT[A/C]ATGGAAGAATGCTTA	23077
rs145512194	snp	C/T	0.00557542	0.0525036	intron-variant	MYCBP2	GRCh38.p7	13:77298995	AAATAAAACACAATA[C/T]GTATTCTTCATACTA	23077
rs145572767	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77050873	AGGATCAAGGAATTC[C/T]TCCTGCTTCTTTAGG	23077
rs145574936	snp	C/G	0.00795532	0.062565	intron-variant	MYCBP2	GRCh38.p7	13:77142210	ATGTCTTGTGTGTCA[C/G]TACTTATATTCTACT	23077
rs145612391	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77152910	CTCTACTAAAAATAC[-/A]AAAAATTAGCCAGGC	23077
rs145619884	in-del	-/GGAAAGGAAAGGAAA	0.0391387	0.134304	intron-variant	MYCBP2	GRCh38.p7	13:77285858	AAAGGAGAAAGGAAG[-/GGAAAGGAAAGGAAA]GGAAAGGAAAGGAAA	23077
rs145621832	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77222885	TTCTCTTTCTTTCAC[C/T]GTATGTAAAGGAGAA	23077
rs145635858	snp	C/T	6.78081e-05	0.00582232	intron-variant	MYCBP2	GRCh38.p7	13:77068880	TAGGGTTAGTTTGAT[C/T]TACTACTCCTAGCAA	23077
rs145655803	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77117414	AAGGTGGATAAAGTA[A/G]TGAATAATATCATTT	23077
rs145662101	snp	C/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77275801	CCAGCCTGGCCAACA[C/T]AGTGAAACCCTGTCT	23077
rs145667096	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77093404	TTTTTAATCTCTTTC[A/G]TAACAGGAAAAGCAG	23077
rs145679206	snp	C/G	0.125182	0.216612	intron-variant	MYCBP2	GRCh38.p7	13:77199976	TGGAAACTCTAAAAA[C/G]CAGAGCAACTCTCCT	23077
rs145680205	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77258635	TTCACCTTTCACTAG[C/T]TTAGGTCTTTTTGTT	23077
rs145705006	in-del	-/CAAT	0.0482946	0.147699	intron-variant	MYCBP2	GRCh38.p7	13:77258459	CATCTTTAACATTAA[-/CAAT]CAAAGATTATTATTT	23077
rs145711874	snp	C/T	0.0182019	0.0936463	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77077090	AAATATTTTGTTACA[C/T]TCTTAAAATATATTA	23077
rs145749793	snp	C/T	0.0146672	0.084371	intron-variant	MYCBP2	GRCh38.p7	13:77094521	CAATCTTAACCTGGG[C/T]TACAGAGCCCGACAT	23077
rs145766473	snp	A/G	0.0103295	0.0711199	intron-variant	MYCBP2	GRCh38.p7	13:77277604	CTAAATAGCCAAGTC[A/G]GAAAAAAAGGACCAA	23077
rs145808306	in-del	-/CTATGTGACTTT	0.0944967	0.195752	intron-variant	MYCBP2	GRCh38.p7	13:77153706	TTATTCTTGTATTTC[-/CTATGTGACTTT]CTCTTGTCAATAAAT	23077
rs145809048	snp	C/G/T	0.000116217	0.00762209	synonymous-codon, missense	MYCBP2	GRCh38.p7	13:77190317	TGATTTCTTTGAACT[C/G/T]TTGAACTGGAAAACA	23077
rs145814887	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77162408	TTCTCCTTTATTAGT[C/T]AATATAGAACATATT	23077
rs145826223	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77288480	CTGACTTGCAGAAGA[C/T]ACATTATGTGACACA	23077
rs145840125	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77303755	CTCCTTTTGCATACA[C/T]ATAAATGCATATACT	23077
rs145900781	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77073038	CATCTGTTTAAAGCA[C/T]AGAATTCAATGGTTT	23077
rs145909398	snp	C/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77171284	AAGAAAATAAGAATA[C/T]ATGGTAACTCCTTTT	23077
rs145948114	snp	C/T	0.00835141	0.0640778	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77082919	GCACCATCTATATAA[C/T]GTAGGGATTCTATCT	23077
rs145949314	snp	C/T	0.00597247	0.0543191	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77085785	ACTTGAAGCACACTA[C/T]GTAACCAAAACAGGA	23077
rs145957420	snp	C/T	0.0130921	0.0798413	intron-variant	MYCBP2	GRCh38.p7	13:77313880	ACCGAACAAGATATA[C/T]AGATGGCAAATAAGC	23077
rs145975915	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77080304	CCAATCCTACCACTG[C/T]GGCTCTTCCTGAGAA	23077
rs145976056	snp	C/T	0.0267878	0.112589	intron-variant	MYCBP2	GRCh38.p7	13:77137532	CCAAGGTAAGATGAT[C/T]GCTTGAGCTCAGGAG	23077
rs145989990	snp	C/T	0.0588605	0.161139	intron-variant	MYCBP2	GRCh38.p7	13:77155156	CTTTTCCATACAGTT[C/T]TATTTACTGGTCTTA	23077
rs145990671	snp	A/G	0.0256215	0.110247	intron-variant	MYCBP2	GRCh38.p7	13:77240424	ACCAGCCTGGCCAAC[A/G]TGGTGAAACCTCGCC	23077
rs146002243	snp	C/T	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77296824	CTTTACATACACATA[C/T]AAGATACTAACATAT	23077
rs146009453	snp	A/C	0.00191606	0.0308927	synonymous-codon	MYCBP2	GRCh38.p7	13:77098418	TCTATTTTCAGATCC[A/C]GGGGAATCTGTAGAA	23077
rs146013862	snp	C/T	0.000940152	0.0216608	intron-variant	MYCBP2	GRCh38.p7	13:77150957	ACTTCCACCTAAACA[C/T]GGTATTATAGAAACC	23077
rs146022222	snp	C/T	0.00318978	0.0398085	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77078142	ACAAACACAATCTCA[C/T]TGAATAGGATTATTT	23077
rs146027799	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77167923	ATCCTTCTCTTCCTT[A/C]ATTTGCATGATACAA	23077
rs146029068	snp	A/G	0.0376037	0.131863	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77292811	AAAAATACAAAAATT[A/G]GCTGGACGTGGTGGC	23077
rs146032966	snp	C/T	0.000891074	0.0210889	synonymous-codon	MYCBP2	GRCh38.p7	13:77061194	TCGGAATTCCACCAT[C/T]GCCTTCATTGTTTTA	23077
rs146037336	snp	C/T	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77222858	TTTATTTAATGACTA[C/T]GTGAAGGTAAGTTCT	23077
rs146060379	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77261817	TTGTCACAAACCTTC[A/G]ATTTGTAAAAAGAGC	23077
rs146074719	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77106230	TGAGTCAACAACTAA[A/G]CAATGATTGGAAATG	23077
rs146085110	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77159310	ATTGCCTAACAAATA[A/G]TAAGTGTTTAATACA	23077
rs146085601	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77102643	TAAAATATTAAAACT[C/T]AGTCACTAGGAAAAC	23077
rs146110113	snp	G/T	0.00438332	0.0466095	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77086114	AGATATGCCCTCATA[G/T]TTACACTTTCTTTTC	23077
rs146112679	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77172512	AGAGAACTGATTGTA[A/G]GAGACCAATAGTGAA	23077
rs146115956	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77219286	AATGCTCTAAGGAGA[C/T]ATACACCTAACCACT	23077
rs146119710	snp	A/G	1.83444e-05	0.00302851	synonymous-codon, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326530	GTCATTGAGCGCAGC[A/G]GTATAAATCCTCCGG	23077
rs146123250	snp	A/G	0.021333	0.101051	intron-variant	MYCBP2	GRCh38.p7	13:77225633	AATCAGTTTATTATG[A/G]AAGAACAAGAGAAAA	23077
rs146126892	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77316350	CGATCAACCAGTTCA[C/T]TCAGGCTGCCCCCAA	23077
rs146150082	snp	C/T	0.0103295	0.0711199	intron-variant	MYCBP2	GRCh38.p7	13:77221453	GAAGGATGTTGTGCT[C/T]ATGCTGCTCATTCTT	23077
rs146231409	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77107026	GTTTATGTATTTATA[C/T]ATATTTCTTTAGATA	23077
rs146232428	snp	A/G	0.00636936	0.0560724	intron-variant	MYCBP2	GRCh38.p7	13:77196741	GGCAGATCATCAGAA[A/G]CATAGTATTGAATAT	23077
rs146244484	snp	G/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77246059	TGACTTGGGGTCAGG[G/T]AAAGTAACTTCTTAG	23077
rs146270363	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77241755	CTTCATGTGCCAAGT[A/G]TATGTTTTACAATTT	23077
rs146309631	snp	A/C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77188698	GATTTACTAGAAAAG[A/C/T]AAATCGTTATTTGTT	23077
rs146310432	in-del	-/AATTA	0.0678174	0.1712	intron-variant	MYCBP2	GRCh38.p7	13:77144286	AAATGTTAATGCACT[-/AATTA]AATACTCATTATGAA	23077
rs146312878	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77063197	CTTGTTGCCCCAGAA[A/C]GCCTAATACTATACT	23077
rs146339203	snp	C/T	1.71337e-05	0.00292687	missense, utr-variant-5-prime	MYCBP2	GRCh38.p7	13:77278899	AAACTTCACAAAGGC[C/T]AACCTCAATAATCTA	23077
rs146339409	snp	G/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77058679	CATATTTGTCATCAT[G/T]CACAGCTATAAAGCA	23077
rs146339860	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77111477	GGGTCTTGCTCTTTT[C/T]GCCCAGGCTGCTCAC	23077
rs146354817	snp	A/C	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77221158	CAATGTTTAATCTTC[A/C]TAAGAAACCCTGATA	23077
rs146366893	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77272083	GATTGAGCATAAATA[C/T]TGGAGACAGATAAGC	23077
rs146392778	snp	A/G	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77267688	ATGTATTAACTTCAC[A/G]TAGACTATAAAATGC	23077
rs146414199	snp	A/C	0.00438332	0.0466095	intron-variant	MYCBP2	GRCh38.p7	13:77193694	TCAGTAAAGCTAGTC[A/C]CCTCCCCAAGTGTGT	23077
rs146414292	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77142224	ACTACTTATATTCTA[C/T]TTCATAAGATTTTTG	23077
rs146429663	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77282891	TATTACTAATTCCTG[C/T]CAATTCTGCTTAACA	23077
rs146440953	snp	A/G	0.00557542	0.0525036	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77327992	ATATGCTCTAGAAAT[A/G]TACGTGCCAATGCAC	23077
rs146458777	in-del	-/TA/TATATA/TGTA	0.495999	0.0445491	intron-variant	MYCBP2	GRCh38.p7	13:77071237	GTATATATGTGTGTG[-/TA/TATATA/TGTA]TATATATATATATGC	23077
rs146476533	in-del	-/ACAC			intron-variant	MYCBP2	GRCh38.p7	13:77166967	TACTTCAAAGACAAA[-/ACAC]ACACATACACACACA	23077
rs146482643	snp	C/T	0.000283388	0.0119001	synonymous-codon	MYCBP2	GRCh38.p7	13:77095366	TTATTACCTAGCTAA[C/T]GTCTGCAGGTAGAGA	23077
rs146511284	snp	A/C	8.67817e-05	0.0065866	intron-variant	MYCBP2	GRCh38.p7	13:77055810	CAGAATCATTTATTA[A/C]CCAACTCAACAAACA	23077
rs146512442	snp	C/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77145365	ATCTCACTGGCCATT[C/T]TTTGTCAGTGTTTTG	23077
rs146551145	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77212248	AGTAGATAAAAATCA[A/G]TCTATGAAACCTTAT	23077
rs146618319	snp	A/G	0.00153338	0.0276467	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081408	GCTAAAGAGCCGTAA[A/G]TCACGTTTGCTTTCT	23077
rs146625544	snp	C/T	0.000386766	0.0139008	missense	MYCBP2	GRCh38.p7	13:77191782	CAGCTTGCAGGAGAA[C/T]AGGCTCATCAAACAT	23077
rs146633340	snp	G/T	0.00382932	0.0435889	synonymous-codon	MYCBP2	GRCh38.p7	13:77166522	AGGGTCAAATTCGAT[G/T]GTCATCCACCTCACA	23077
rs146636859	snp	C/T	3.30628e-05	0.00406575	synonymous-codon	MYCBP2	GRCh38.p7	13:77260576	TTTATAAGGTTTGGA[C/T]TGCCGTCTGCTCTTA	23077
rs146644162	snp	A/C	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77162994	TGGGACCTTCTTCTG[A/C]AACTTGCTTTTCTCA	23077
rs146646456	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77308043	GTTCAATAAGCTATA[A/G]CAACCCTAAACAATA	23077
rs146669237	snp	C/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77234787	CAGATATATAAATTA[C/G]TATAAAAAGTATTTT	23077
rs146672811	snp	A/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77322339	ATTGTTTTCACTAAC[A/T]TTGTTCTTCTAGGAC	23077
rs146684390	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77195137	CAAGTACTGTGCTAG[A/G]TGTCTAAATTTTTAA	23077
rs146714359	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77055011	CAAAAATTTTGGGGG[A/G]TCATAAACATATACA	23077
rs146740296	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77103136	GAACATGACTGAGAC[A/G]AACGGAAACATCTTT	23077
rs146740809	snp	C/T	0.0271762	0.113356	intron-variant	MYCBP2	GRCh38.p7	13:77050263	CTGATAGGCAGCAGA[C/T]GGCAGTGTGTGTTTT	23077
rs146752347	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77100058	GAAAAGCAATCTGAC[C/T]GAAGGGTTTCAAGTG	23077
rs146753203	snp	C/T	0.00478085	0.0486577	intron-variant	MYCBP2	GRCh38.p7	13:77187871	TCGAGGTCAGGGGTT[C/T]GAGACCACCACCAAC	23077
rs146760457	in-del	-/AAGCTATCGGAACACCAAGTCATCAAAGA	0.0622301	0.165053	intron-variant	MYCBP2	GRCh38.p7	13:77071113	TAGTGGTCTTAAATT[lengthTooLong]AATGTATCATAAGGA	23077
rs146763428	snp	C/T	3.30497e-05	0.00406494	missense	MYCBP2	GRCh38.p7	13:77098470	TTTGGTGACGTTGAC[C/T]GTCCTCTCAAAGGTT	23077
rs146765497	snp	C/T	0.0271762	0.113356	intron-variant	MYCBP2	GRCh38.p7	13:77182654	AGTTGTGCACTAGTC[C/T]AGGCAATAATCTTGC	23077
rs146765544	snp	G/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77238596	GTTATCACAAACCAT[G/T]GAACTAAAATCTATA	23077
rs146766860	snp	A/G	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77325817	CGGTTATCAAAGTAC[A/G]GCTCTAAAAATCTCT	23077
rs146792401	snp	A/T	0.00636936	0.0560724	intron-variant	MYCBP2	GRCh38.p7	13:77257926	GTTTATTTCTGGGGC[A/T]AAATAACTCAACAAA	23077
rs146798180	snp	A/G	4.96981e-05	0.00498463	missense	MYCBP2	GRCh38.p7	13:77095601	CTCCTAGATTGTTTG[A/G]CCTGGCGAAGAAAAA	23077
rs146803783	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77308391	AGATAGGTTAAGAGT[A/G]CAGAATTTAGAAACA	23077
rs146834921	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075959	GGTGAGACAAGGGAA[A/T]TCCTTGAAATTTATC	23077
rs146841995	snp	C/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77101261	GTTTTCTCTCTAATT[C/T]ATAAAAAAGGACAAC	23077
rs146860872	snp	C/T	0.0115144	0.0749975	intron-variant	MYCBP2	GRCh38.p7	13:77125174	AGTACTCACGTATTT[C/T]ACAAACCAATTTTAA	23077
rs146861129	snp	A/G	0.0271762	0.113356	intron-variant	MYCBP2	GRCh38.p7	13:77072267	CTGCACTCCAGCCTG[A/G]GCGACAGGGCAAGAC	23077
rs146865501	snp	C/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77189444	TATTACAAACAGTAA[C/T]TATAACAGATTGCAC	23077
rs146871678	in-del	-/G			intron-variant	MYCBP2	GRCh38.p7	13:77314786	TGATGTGTCAGTGGA[-/G]GGTTAAACAATGGCC	23077
rs146873025	snp	C/T	0.0271762	0.113356	intron-variant	MYCBP2	GRCh38.p7	13:77120372	TCCTTCATAAAAATA[C/T]TTTGTGGAAAGTAAT	23077
rs146875296	snp	A/G	0.00597247	0.0543191	intron-variant	MYCBP2	GRCh38.p7	13:77211593	GATAACTTGGTCTTC[A/G]TGAAATTTCAAAGTT	23077
rs146887259	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77265267	AGAACACAAAGAGGC[A/G]CAAGAAAGATGCTTC	23077
rs146899884	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77239334	AAGTATCAACAGGCC[A/G]AAGAAATAAAAGATC	23077
rs146901215	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77328853	GAGATTGAGGGAGGA[A/C]TTAAAGGATCTAGGA	23077
rs146923342	snp	C/G	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77314739	AACCCCAAGAGTGAA[C/G]CCTAATGTAAACTCT	23077
rs146949484	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77060829	TTGTGGGGCAACAAC[C/T]AGCAGAACTAGAAGG	23077
rs146959275	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77056087	GCCACAAATAAGACA[C/T]GCTCTGTGTTTGGTG	23077
rs146971407	snp	A/G	0.0142736	0.0832652	intron-variant	MYCBP2	GRCh38.p7	13:77128108	ATATATATTTGTAAG[A/G]ATTTATATATATGCA	23077
rs146972135	snp	A/G	0.000198416	0.00995834	missense	MYCBP2	GRCh38.p7	13:77270039	TTCTGTTTCTAATAC[A/G]GGATGTAGAATTGTA	23077
rs146973705	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77218649	TCCTGTGAACAGTAA[A/G]GAGGCCCATACGTGT	23077
rs146996747	snp	G/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77270659	TCAGAATGATATTTC[G/T]CATGCCAGCAAAAAG	23077
rs147004512	snp	A/C	0.00597247	0.0543191	intron-variant	MYCBP2	GRCh38.p7	13:77171935	AGACAGAGTCTTGCT[A/C]TGTCGCCCAGGCTGG	23077
rs147005501	snp	A/C	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77267038	GTAGCTCTCACTTTC[A/C]GATGGTCAAACGCTT	23077
rs147067099	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77077787	GGTTCTTTTTTTGTG[C/T]ATCCTCACATTAAAG	23077
rs147075646	snp	A/G	4.99988e-05	0.00499969	missense	MYCBP2	GRCh38.p7	13:77098990	AGGCTGGTTTAGAAG[A/G]TGTTGAGATGTTTCC	23077
rs147076719	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77152695	GAGACGGCTGGGCTT[C/T]AGGGAAATATCACCT	23077
rs147087914	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77061551	TGTGAACTCAACCAA[C/G]GTCTTTGATTCCAAA	23077
rs147094928	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77056490	TTAGCTTGCCAAAAC[A/C]ACTTCCTACTTGCTG	23077
rs147098289	snp	A/C	0.000153988	0.00877328	synonymous-codon	MYCBP2	GRCh38.p7	13:77156106	CTGGTCTTTTGTTTG[A/C]ACAGTTATGGTGGTA	23077
rs147099220	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77147678	GTCTTTAGCCATACA[A/C]AGGTGAGAAAAGGAA	23077
rs147099586	snp	C/T	0.0422008	0.138995	intron-variant	MYCBP2	GRCh38.p7	13:77199322	CCCACCTGAATACTG[C/T]ACTTTTCTGACGGGC	23077
rs147100704	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77294876	TATTCACCAGGGTGC[G/T]CACCCACTGCCCATC	23077
rs147130319	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77070402	TTCTTAAAGTATTAG[C/G]AGATTTTTTTTTCTT	23077
rs147130447	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77161401	AAGCAAACAATAATA[A/C]AAACAACAAATGATG	23077
rs147131716	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77213747	ACTGGAGGACAATGA[C/T]TGTCTGACGTCAAAT	23077
rs147143036	snp	G/T	0.00874735	0.0655527	intron-variant	MYCBP2	GRCh38.p7	13:77301765	CTCACAGAAAACCCA[G/T]ATATTAACGTTAGGA	23077
rs147147421	snp	A/G	3.37086e-05	0.00410526	missense, nc-transcript-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087552	GTTCCACTGGTGCAG[A/G]AGTCAGTGATGCCAC	23077
rs147169898	in-del	-/A	0.0130921	0.0798413	intron-variant	MYCBP2	GRCh38.p7	13:77282985	CTGCAATAACTGCCT[-/A]AATGGTTCCTCTGTC	23077
rs147212736	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77164891	ATAGCCAACTGAGCA[A/G]GTTCAGGGCAGGTAT	23077
rs147225376	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77074727	GATAAATCTCAAAAG[C/T]ATTACACTAAAGTGA	23077
rs147226003	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77306339	TTATCTCATTACTAA[A/G]TAGAAAACTTTTATT	23077
rs147234242	snp	A/G	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77093419	ATAACAGGAAAAGCA[A/G]CACATGTAAATCATA	23077
rs147236415	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77236557	CAACTTTATTCATTA[C/T]AGCAACATTTTAAAA	23077
rs147246406	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77232334	TTAAGAAAATGGGAG[C/T]TTTAAGTTGTGCTAG	23077
rs147258516	snp	C/T	0.0189856	0.0955633	intron-variant	MYCBP2	GRCh38.p7	13:77143959	CTGACCAAAATGCTA[C/T]GAGGTACATGACTGT	23077
rs147276224	in-del	-/TTT	0.0221141	0.102801	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77327724	TTTTTTAAATTACTC[-/TTT]TTTATTGACTCCTCA	23077
rs147280171	snp	A/C	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77280903	GTTTAACAAATGGGA[A/C]AACATTCATTTTCAG	23077
rs147297931	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77052344	GCTAGGATCATAGGT[A/G]CACGCCACCACACCC	23077
rs147307074	in-del	-/CT	0.158962	0.232835	intron-variant	MYCBP2	GRCh38.p7	13:77148510	CTCTTACTTCCTTGA[-/CT]CTCTGAAATTTCTTC	23077
rs147308178	snp	A/T	0.0126979	0.078662	intron-variant	MYCBP2	GRCh38.p7	13:77049124	CTCCAAGCTCAAGTC[A/T]TCTAGAGTCATCTAG	23077
rs147331532	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77097109	GACAGACACATTAAT[G/T]GCACACCCTTTGGGT	23077
rs147341605	snp	A/C	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77113882	GTGACAGATGTTATA[A/C]AGTCAAGTGGAAAAG	23077
rs147341706	snp	A/G	0.00558539	0.05255	intron-variant	MYCBP2	GRCh38.p7	13:77168402	CCAAGTTTTACATTC[A/G]AATCACACTAAGAAC	23077
rs147344299	snp	C/G/T	0.00557542	0.0525036	intron-variant	MYCBP2	GRCh38.p7	13:77260762	TAAAATCAGTGAACC[C/G/T]GCTAGCCTCATCTGG	23077
rs147354596	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77254487	TAAAATATTCCTTTA[C/T]GTTCGTTTTAAATTG	23077
rs147364305	snp	C/T	0.00033416	0.0129216	intron-variant	MYCBP2	GRCh38.p7	13:77165417	TGCCAGAATTGAGTT[C/T]AAACTCTAAAACAAT	23077
rs147377745	snp	C/T	0.00597247	0.0543191	intron-variant	MYCBP2	GRCh38.p7	13:77306717	TGTAACACTTTCTAA[C/T]GATATCATGAATACA	23077
rs147387384	snp	A/G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77303494	CAAGTCTAAACAAAT[A/G/T]TCCAAGGACTGAATG	23077
rs147435974	snp	C/G	3.29663e-05	0.00405981	missense, intron-variant	MYCBP2	GRCh38.p7	13:77233216	TGAGTCTGGCTAGAG[C/G]CTGTTCTCGATGGTT	23077
rs147436641	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77118278	CTAATTAGTAACTGA[C/T]AAGCAACTCAGAACA	23077
rs147444569	snp	C/T	0.040671	0.13668	intron-variant	MYCBP2	GRCh38.p7	13:77049834	AGAGATGGGGTTTCA[C/T]CATGTTGGCCAGGCT	23077
rs147448479	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77139394	GTCCTATGAGGCTAG[C/T]AAGGTCTGAAAGTCT	23077
rs147448730	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77189559	AGGGAGATAGAATCA[C/T]AGTTCTAGACCATTT	23077
rs147450769	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77284884	ACTGAGGCACGGATG[C/T]GTCAAATAACTTCCA	23077
rs147463840	snp	A/G	0.000153988	0.00877328	missense	MYCBP2	GRCh38.p7	13:77181858	ACAGACGTGTGACAC[A/G]GAGCTGACATAACAG	23077
rs147482821	snp	C/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77324173	GACCTGAAAACGGTT[C/T]TCACTTTCTTCAACA	23077
rs147492112	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77320966	GCGGTCAGTAACCAG[A/G]GGTAGGAGGGCCTGA	23077
rs147540066	snp	C/T	0.000153988	0.00877328	missense	MYCBP2	GRCh38.p7	13:77098069	CAGCTCTGGCACATT[C/T]GGCCACAGAAGGAGA	23077
rs147551721	snp	C/T	9.90099e-05	0.00703528	synonymous-codon, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076781	TTCTCCTTCAGGTGA[C/T]GACAATAGTGCTTTT	23077
rs147575241	snp	G/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77066184	GAATGCAGCATTTTA[G/T]ATTTTTAAGTGACTG	23077
rs147576294	in-del	-/A	0.101658	0.201233	intron-variant	MYCBP2	GRCh38.p7	13:77241850	AAAAAGAATAGCTAG[-/A]AAAAAAATATAATGA	23077
rs147582397	snp	G/T	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77061063	CAATGATGTCATAAT[G/T]AAACATCAGAATATC	23077
rs147594639	snp	C/G	1.64874e-05	0.00287113	missense	MYCBP2	GRCh38.p7	13:77058354	TCGTTTTTAACACCC[C/G]CGCATGGATGGCCAC	23077
rs147596695	snp	A/G	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77199027	TTAGTATTACTGTAG[A/G]GGGGGAGGAGGCAAG	23077
rs147619895	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77275565	GCAGCAGTGTGTACC[C/T]ATAGTCACAGCTACT	23077
rs147629519	snp	A/G	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77270832	TGTGGAACTCAGATT[A/G]TATTACATTAGATTT	23077
rs147679930	snp	C/T	0.00517822	0.0506191	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77086550	CTCTTCCATTCTGTC[C/T]TCTCCTTCTGAAACT	23077
rs147689670	snp	A/G	0.00279162	0.0372561	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77082171	TTTTTGAGAAATAAA[A/G]GTAACTTCTTTGGAA	23077
rs147689929	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77140443	TAAGAAGGATAAAAA[A/C]CATTTCTTTCTGTTA	23077
rs147691450	snp	A/G			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228230	TTCTGCTCAAGCTGG[A/G]CATGGTGGTTCACAC	23077
rs147701329	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77222584	ACATATAGAATCTGG[A/G]GACCTTTTAGAAAAA	23077
rs147711528	snp	C/T	0.0103295	0.0711199	intron-variant	MYCBP2	GRCh38.p7	13:77157608	AAAAAGAAAAATAGC[C/T]GGGTGTGGTGGCATA	23077
rs147724831	snp	G/T	0.0217236	0.101931	intron-variant	MYCBP2	GRCh38.p7	13:77299320	AATACTTCTTTCTAT[G/T]CATGATGGCATTTAA	23077
rs147733575	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77294939	AGTATCCCGTATCTC[C/T]GTGGTCAAAGCAAAT	23077
rs147783851	snp	C/T	0.0130921	0.0798413	intron-variant	MYCBP2	GRCh38.p7	13:77109814	TCCCCAAATTAATAC[C/T]TTTATAATTTCTTAC	23077
rs147793109	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77162119	TGGCATACAGTTTAA[C/T]ATATAAGATACTTCC	23077
rs147793615	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77104497	AGTCATATGCCTACA[A/G]ATGTGTCATTCTCCA	23077
rs147796654	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77248929	ATAGAATATTATTCA[A/G]CCTCAAAAAGCAAAG	23077
rs147806803	snp	A/G	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77243375	CCCAGCACTTTGGGA[A/G]GCCAAGGTGGGCAGA	23077
rs147816670	snp	C/T	0.00106576	0.0230596	intron-variant	MYCBP2	GRCh38.p7	13:77174287	ACTGTAAAGTATTTC[C/T]GTTATCTCTATACAT	23077
rs147829617	snp	A/G	0.0681886	0.171594	intron-variant	MYCBP2	GRCh38.p7	13:77317714	GAGGCTGACGTGGCC[A/G]GATCACGAGGTCAGG	23077
rs147839519	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77313994	CCAAAATCCAGAACA[C/T]AGACAACATCAAATG	23077
rs147877804	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77134302	TGGGAAGCCAAGGTA[A/G]GTGGATCACTTGAGG	23077
rs147886448	in-del	-/CA	0.467642	0.123012	intron-variant	MYCBP2	GRCh38.p7	13:77310786	GTGTGCGTGCGCATG[-/CA]CACACACACACACAC	23077
rs147887434	snp	G/T	0.000399281	0.0141238	downstream-variant-500B	MYCBP2	GRCh38.p7	13:77044596	CTTTCTGAGGAAAAC[G/T]GGACTTTTAGACCTT	23077
rs147900947	snp	G/T	0.0119091	0.0762411	intron-variant	MYCBP2	GRCh38.p7	13:77180785	GTTAGCTGGGTGTGG[G/T]GGTATGTGCCTACAG	23077
rs147901208	snp	G/T	0.00835141	0.0640778	intron-variant	MYCBP2	GRCh38.p7	13:77128043	AACACTCAAAAAACT[G/T]AGATTTACAACCGAA	23077
rs147901983	snp	A/C	0.00128207	0.0252862	missense	MYCBP2	GRCh38.p7	13:77273516	TGTTGGTGAGGATAG[A/C]AGAGATGGCCTGAAG	23077
rs147903867	snp	G/T	0.00065874	0.0181366	missense	MYCBP2	GRCh38.p7	13:77150862	CAGCTGTTACTGCAG[G/T]ACTGCCAGGAATCCT	23077
rs147933894	snp	A/G	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77249950	AGTTCATGGCCGGGC[A/G]CGGTGGCTCACGCCT	23077
rs147944066	snp	C/T	0.000393504	0.0140213	intron-variant	MYCBP2	GRCh38.p7	13:77243789	CAGTGTAGCATAGTA[C/T]AATCAATCAAAATTA	23077
rs147976490	snp	A/G	0.000197703	0.00994045	synonymous-codon	MYCBP2	GRCh38.p7	13:77125364	GAGGTACTGGTTTCC[A/G]CCTCTGTCTCTAGCT	23077
rs147986932	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77223702	AACTTATCTCTGTGA[C/T]GACTTCTTTAGTTTC	23077
rs148009867	snp	C/T	3.61651e-05	0.0042522	missense	MYCBP2	GRCh38.p7	13:77206820	TCTCTAGTATTTGGT[C/T]GAAACCTTTAAAGAA	23077
rs148015779	snp	A/G	0.00557542	0.0525036	intron-variant	MYCBP2	GRCh38.p7	13:77091644	ACAAAGTTATTTCCA[A/G]ATATTTCCAGATGTC	23077
rs148050936	snp	C/T	0.000148303	0.00860985	missense	MYCBP2	GRCh38.p7	13:77066018	CCTTGATAAGTTTAA[C/T]GATGATCTCTGAGAT	23077
rs148069555	snp	A/G	0.0349115	0.127424	intron-variant	MYCBP2	GRCh38.p7	13:77172058	GGCATGCACCACCAC[A/G]CCCAGCTAATTTTTC	23077
rs148072855	snp	C/G	0.0744748	0.178019	intron-variant	MYCBP2	GRCh38.p7	13:77301409	GCCTGGGCTACAGAG[C/G]AAGACTCCATCTCAA	23077
rs148093218	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77189621	ACATTTTTCAGTAAC[A/G]GTTTATATCCATTTG	23077
rs148102361	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77239500	TCCAAGACCCTTGAC[C/T]CATAAATTCTGATTC	23077
rs148107342	in-del	-/TAAACATA	0.0614824	0.164198	intron-variant	MYCBP2	GRCh38.p7	13:77206973	CTTCTGGATCTAAGC[-/TAAACATA]TAAAAAAACTATATC	23077
rs148120265	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77167818	ATGATGGATAAACAA[A/G]TGCACTGTACTAGCT	23077
rs148124113	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77259084	ACACAGTGAAACCTC[C/G]TCTCTACTAAAAATA	23077
rs148132880	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77048622	GTTCTTAGGCCAGTT[C/T]ATTAACCTCCCTAGC	23077
rs148144092	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77183644	GCAACCTTCACCTCC[C/T]GCCTTCAAGCAATTC	23077
rs148157671	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77323445	ATAAATTCCCAGAAC[A/G]TTCTTCCTCTACATC	23077
rs148164631	snp	A/G	0.0154538	0.0865337	intron-variant	MYCBP2	GRCh38.p7	13:77110660	CTCAGAGGACATCAC[A/G]GTCCTACCAATATGT	23077
rs148199676	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77271230	GCTAATTCTCAATAA[C/T]GGTGCCTTTTTCCAT	23077
rs148227333	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77138066	AAAATTTAATAAGAC[A/G]TAATTGATGTAATTT	23077
rs148238922	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77121901	ATATTAGTATTAGAA[C/T]AGAGAAAAAAACTAA	23077
rs148260306	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77234844	TTAAGGTAATAATAT[A/T]GTTATATTACCATTT	23077
rs148280869	snp	C/T	0.000399281	0.0141238	intron-variant, missense	MYCBP2	GRCh38.p7	13:77129191	AAGTCCATGAAAATA[C/T]GTCCAAATCCCTGAC	23077
rs148285213	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77253823	TGGAAAATCCAACTC[C/T]ACTGGTGAGAGTATA	23077
rs148315280	in-del	-/AGCCT	0.0146672	0.084371	intron-variant	MYCBP2	GRCh38.p7	13:77143781	TGGGTTATATGGTAC[-/AGCCT]AGCCTATTGGTCTTA	23077
rs148315706	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291341	GGAAACCCCTACTTA[A/G]TAGGCTGACTAAAAT	23077
rs148320479	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77073808	TGTTAAATGTTTAGG[A/C]ATAAATTTAATAAAA	23077
rs148333398	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77212975	GAACACTCTGGTCAC[A/G]TTCTCATCCAACCAC	23077
rs148354925	snp	A/C	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77143225	CCTGGTAAGGCATTA[A/C]TTTTGCGTCTGTGAG	23077
rs148357162	snp	A/C	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77231494	TCAAGTGATCCACCC[A/C]CTCAGCCTTCCAAAG	23077
rs148366858	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77284525	CTGAAAGTTTCACTC[C/G]CCACCCATAGTATCT	23077
rs148372975	snp	A/C	0.0337553	0.125452	intron-variant	MYCBP2	GRCh38.p7	13:77068009	CACAGCTCACTGCAG[A/C]CTTGAACTCCTAGGC	23077
rs148374262	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77158184	TTTTTCAACATGCAG[A/G]TACTTTCAGATAGGC	23077
rs148405843	in-del	-/CAC	0.0146672	0.084371	intron-variant	MYCBP2	GRCh38.p7	13:77324114	ATTCCATTCACTCCT[-/CAC]CACATCCCTCTATTC	23077
rs148406683	in-del	-/CTCCACTAC			intron-variant	MYCBP2	GRCh38.p7	13:77223917	AAACTAAAACTAAAA[-/CTCCACTAC]CAAATGAAGTAGGGA	23077
rs148416281	snp	A/G	3.30071e-05	0.00406232	synonymous-codon	MYCBP2	GRCh38.p7	13:77093221	TACATTAGGACTTGC[A/G]TCAGGAGTTACTGAT	23077
rs148416822	snp	A/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77165501	ATAGGTAAAAACACA[A/T]ATCATATACTACATA	23077
rs148422358	snp	G/T	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77293343	ACTTGAGATTGATGA[G/T]CATGAATGTGTATCA	23077
rs148428108	snp	G/T	0.0275645	0.114116	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075680	ATTTCTTTTTGGGGG[G/T]GGTGAGGGGAATGCA	23077
rs148429310	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77306739	ATGAATACAATCTAT[C/T]CATCCCAGGCCTCAG	23077
rs148440093	snp	C/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77214854	TAGTCAAAGTACTTA[C/T]TATAATCTTATGGGA	23077
rs148451019	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77232994	AAGCATGACAGTCAC[C/T]GACAAACGGTATCAC	23077
rs148456186	in-del	-/TAT	0.00438332	0.0466095	intron-variant	MYCBP2	GRCh38.p7	13:77270182	TGGTTTTCAAATAAA[-/TAT]TATTACACTAAAATT	23077
rs148460099	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77107904	AACTTAGGAGGAATA[C/T]GGAATTATGTGAATG	23077
rs148460530	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77144619	AAGCAGTCAACATCA[G/T]TACGATAGTTCAGCA	23077
rs148470203	snp	A/G	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77160041	AGCTCCCTATGATCA[A/G]AAGACAGTGTTCAAA	23077
rs148471490	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77246125	TTCATCAGATCAGTT[A/C]TTGAAACTTTTGACA	23077
rs148509999	snp	C/T	0.00755907	0.0610114	intron-variant	MYCBP2	GRCh38.p7	13:77102563	AGTGTTTCAAAAAAC[C/T]AAAAACATATTTTTA	23077
rs148527512	in-del	-/TACAATAA	0.0422008	0.138995	intron-variant	MYCBP2	GRCh38.p7	13:77268030	TACAGGTTTTTGAGG[-/TACAATAA]TACATCAATATTGAT	23077
rs148594764	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77086325	TTAAGCAATTATTCT[C/T]ACTGTCCCTCTTTTG	23077
rs148595891	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77173702	CATGACTACCTAAGA[C/T]GCCAGCTTTGCCGCT	23077
rs148596992	snp	C/G/T	0.000297616	0.0121952	synonymous-codon, missense	MYCBP2	GRCh38.p7	13:77051883	ATCTCCCCGTCCAGC[C/G/T]TCAGCATCGCAGCGA	23077
rs148625811	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77119375	TTTCTGAAATATAAT[A/G]AAGTTTCATATGTGA	23077
rs148629050	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77242765	AGTTGCCATTTCTAA[C/T]AGTTATTGATAGTAG	23077
rs148650890	snp	A/T	0.000399281	0.0141238	synonymous-codon	MYCBP2	GRCh38.p7	13:77263724	TTTTCTAGCCAGTTT[A/T]AGTTGCAATTCTTGC	23077
rs148659498	snp	C/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77187701	AACAAGCAAGCATGT[C/T]GTAGAGCATCCTGTA	23077
rs148660398	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77280987	ATTAAAGAATTTTTA[A/G]TATTTAGCTATGGAT	23077
rs148666671	snp	C/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77064263	TCTCCAAAGGACCTT[C/T]GGTCTATCACAGCAT	23077
rs148683885	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77325608	ATTCAGATTTTCTAG[C/G]TAGTGGCAGTTGAAC	23077
rs148689057	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77113528	GAAAGATGGTAATGA[A/T]GGGTGAAATAAACAC	23077
rs148700860	snp	C/T	3.31774e-05	0.00407279	missense	MYCBP2	GRCh38.p7	13:77181813	AATACTTCTCCATCA[C/T]ACGCAATCGGGAAGA	23077
rs148720553	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77148695	TCACAAATAATCTTC[A/G]ATTTCAACTGATTAT	23077
rs148754778	snp	A/G	0.000504549	0.0158751	synonymous-codon	MYCBP2	GRCh38.p7	13:77243933	ACAACCAGATTCTCC[A/G]GAACCACAACCACAG	23077
rs148755149	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77140444	AAGAAGGATAAAAAC[C/G]ATTTCTTTCTGTTAG	23077
rs148795923	snp	C/T	1.64969e-05	0.00287196	missense, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081558	AGGTTTCTGTGGAGC[C/T]GTCTGTCAAACTGCC	23077
rs148806068	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77133854	CCATTCCACAACTTA[C/T]CACAATGCAATTTAA	23077
rs148809166	snp	C/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77221635	CCCCATCTTATCTAA[C/T]TGCAATGCACCTTTC	23077
rs148818330	snp	C/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77151627	TGCAAAAAACAGATT[C/T]GTTAATGGATGTTAA	23077
rs148827324	snp	C/T	0.00557542	0.0525036	intron-variant	MYCBP2	GRCh38.p7	13:77060800	TTAGTGATCATCTAG[C/T]GCAGCAATTTTTATT	23077
rs148841867	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77197343	AGTCTTTTTTGTGGA[A/G]AAGAAAGAGATATAG	23077
rs148871856	in-del	-/TCTATTTTCTAATAGACGGC	0.0414363	0.137845	intron-variant	MYCBP2	GRCh38.p7	13:77091131	CCCTTGGTAAAATTA[-/TCTATTTTCTAATAGACGGC]TAACTGCCTAGGTGT	23077
rs148891027	snp	A/G/T	6.59863e-05	0.00574364	synonymous-codon, missense	MYCBP2	GRCh38.p7	13:77098558	ATTTAGAACGTTCCC[A/G/T]AGGAGGATCAAGCTT	23077
rs148903870	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77223012	GAATTGCTGAGTGAA[A/G]TCTGGCTTGAAGCTG	23077
rs148914583	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77136090	TCCCAAAGTGCTGGC[A/G]TAATAGGCGTGAGCC	23077
rs148955084	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77218499	TTAAAGCTAGACTGG[C/T]TGGTTGTGAATCCTG	23077
rs148958125	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77308982	GTGTTTCTTTTCAGG[C/T]AGATAGTCATAGATG	23077
rs148963318	snp	C/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77094539	CAGAGCCCGACATTA[C/G]TTGGGTGAACCAATC	23077
rs148968342	snp	A/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77323115	TTTAATCTACAAAAC[A/T]ATTCATGTTAGTATT	23077
rs148975808	snp	C/T	0.0718919	0.175435	intron-variant	MYCBP2	GRCh38.p7	13:77110274	GGGGAGGTCTATAAA[C/T]GGCTGCTCTGGGAGT	23077
rs148979209	snp	A/T	0.00914312	0.0669923	intron-variant	MYCBP2	GRCh38.p7	13:77235231	TGAAATATTACAATA[A/T]ATGCTATAAAAGAAA	23077
rs149008886	snp	A/G/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77303974	TATACATAACAAAAA[A/G/T]ACAAAAAATAAATGC	23077
rs149027222	snp	C/T	0.004905	0.0492792	intron-variant	MYCBP2	GRCh38.p7	13:77194141	ACAATGAATAATGCA[C/T]AAATTATTTACCTAG	23077
rs149032492	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77317815	GGTGATGTGCACCTG[C/T]AGTCCCAGCAACTCA	23077
rs149038537	snp	A/T	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77103831	ACTTTTCTGGGTCCA[A/T]CTTCAGTGAAAACGT	23077
rs149066307	snp	A/G	0.000266818	0.0115472	synonymous-codon	MYCBP2	GRCh38.p7	13:77263679	GTCCTTTTCCAGATC[A/G]AATAGTGAGATACCA	23077
rs149103585	snp	A/G	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77128652	ACTGACAGACATAAA[A/G]TCATAGAACTGTGCC	23077
rs149113191	snp	C/T	0.0236746	0.106192	intron-variant	MYCBP2	GRCh38.p7	13:77175750	TGGATCACTTGAGGG[C/T]AGGAGTTCGAGACCA	23077
rs149115172	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77270934	TAATTTCTTCCTCTT[C/T]ATCTTTCAGTTCACC	23077
rs149120830	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77055824	AACCAACTCAACAAA[C/T]ACTTAGCATGCACCT	23077
rs149142466	snp	C/T	0.000197674	0.00993972	missense	MYCBP2	GRCh38.p7	13:77150793	TTGGTTCATATGAAA[C/T]ATCTAGCTTTGGTGA	23077
rs149147384	in-del	-/T			intron-variant	MYCBP2	GRCh38.p7	13:77287602	GTGATTTTTTTTTTT[-/T]CCTAATCAAGGGAAA	23077
rs149154041	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77121725	TTAGAAATGAGATAG[C/G]CTCTTATGAAGCCAA	23077
rs149154232	snp	C/T	0.000260804	0.0114164	missense	MYCBP2	GRCh38.p7	13:77097534	TTTTTCTTTTTTTCC[C/T]TTTTGGACTTCTTAT	23077
rs149167244	snp	A/C	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77265871	ATTTTAAGCTTGTAT[A/C]TTCAGGAATATATCA	23077
rs149189180	snp	A/T	1.69424e-05	0.00291048	intron-variant	MYCBP2	GRCh38.p7	13:77188923	AGGACTGAAGAGAAA[A/T]GCTGAAATTTTTTAA	23077
rs149190305	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77284379	TGAGGCACAGAGAAG[A/G]TCAAAGGGAAAAGAA	23077
rs149196565	snp	C/T	0.000280045	0.0118298	synonymous-codon	MYCBP2	GRCh38.p7	13:77174424	CTGAACTGTGGTCAT[C/T]CCTCCATCTCCATTG	23077
rs149197578	snp	G/T	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77066717	AAAGGCTGCAGCAAT[G/T]TATATGAGATGAAAA	23077
rs149200570	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77328757	GCCCTGGAATTGGAT[C/T]CTGACTCTGCTACTT	23077
rs149208660	snp	C/T	0.0130921	0.0798413	intron-variant	MYCBP2	GRCh38.p7	13:77207035	TAGTAACGTAGATTA[C/T]AATACTTAATACAGA	23077
rs149219802	snp	A/C	0.00795532	0.062565	intron-variant	MYCBP2	GRCh38.p7	13:77256906	AAAAGAAAGGAAATT[A/C]GTACATCAAAGAGAT	23077
rs149252726	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77214099	TGAGGATCAGAGCAC[C/T]AACTAAAGGCAAAGG	23077
rs149264610	snp	A/G	0.00557542	0.0525036	intron-variant	MYCBP2	GRCh38.p7	13:77123901	ATATGAAGTAAATAT[A/G]CAGCAATATATAATA	23077
rs149272381	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77142726	AGTGAGACTACCATA[C/T]ACAAGTTGAGCATCT	23077
rs149281685	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77052292	CAGCCTCAACCTCTT[A/G]GGCTCAGGCGATCCG	23077
rs149291522	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77069418	ATGAGATCAGGAGAT[C/T]GAGACCATCCTGGCT	23077
rs149295747	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77159426	TAAAGATCTCTCCAT[A/G]TCTGGTCTAGATGAC	23077
rs149304679	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77209325	TTAGTTATACTGTTA[C/T]TGCTAACTTAGTGAA	23077
rs149313090	snp	C/T			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77083657	AAAAGCTCCTTTCTA[C/T]GCAAATGGACCACAG	23077
rs149333798	in-del	-/T	0.0185938	0.0946107	intron-variant	MYCBP2	GRCh38.p7	13:77047310	TAAAATTATTTTTTC[-/T]GATTCTTAGATACCT	23077
rs149334563	in-del	-/A	0.078151	0.181571	intron-variant	MYCBP2	GRCh38.p7	13:77269936	TGATTAAACAAGGAC[-/A]AATCACATGTTGTAA	23077
rs149338680	snp	C/T	0.00755907	0.0610114	intron-variant	MYCBP2	GRCh38.p7	13:77278542	TTTAAAAACTGCAAA[C/T]TGACAATTTATAATT	23077
rs149346241	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77153479	GATATTAAATTACAG[A/T]CACTATTTTTATACA	23077
rs149349473	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77239452	GTGCCAGAGAAGAGC[C/T]TTAGAACACTGTGCA	23077
rs149359740	snp	C/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77295360	GATGGTCTCGACCTC[C/T]TGACCTCGTGATCTG	23077
rs149386447	snp	A/G	3.32585e-05	0.00407776	synonymous-codon, utr-variant-5-prime	MYCBP2	GRCh38.p7	13:77278822	CAGCACGTTGAGCAG[A/G]GCTTGGAGACTCCTG	23077
rs149435923	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77226823	AAACCTCACTAATTC[A/G]GAATAACATAGAACA	23077
rs149442845	snp	C/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77102053	AAATAATAATGACAG[C/G]ATAGAAACTTAGGGC	23077
rs149473670	snp	C/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77048125	AATGTTATGGTGTTA[C/G]GAGGTGGAGCTGTGG	23077
rs149484278	snp	C/T	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77183020	GCTATATGGAGGAAA[C/T]CATCAATTTGCCTTC	23077
rs149487974	snp	G/T	0.0146672	0.084371	intron-variant	MYCBP2	GRCh38.p7	13:77220947	TCAGTTACCACTCAA[G/T]GGAACAAGGACCAAA	23077
rs149496455	snp	A/C	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77096168	CTTAGTACAAATATT[A/C]AATTTGTATATGATT	23077
rs149499562	snp	G/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77324968	TCTCACGTAGTTTTG[G/T]GCTATTTTCAAAAGC	23077
rs149505488	snp	C/T	0.00557542	0.0525036	intron-variant	MYCBP2	GRCh38.p7	13:77112138	TCTCCATGGTAACTC[C/T]GAGCTGATAAGTGCT	23077
rs149517796	snp	A/G	0.0146672	0.084371	intron-variant	MYCBP2	GRCh38.p7	13:77253256	GTGAGAGAACCAGCA[A/G]TTCTACTCCTAGGTA	23077
rs149528360	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77164326	ATTACCAGTACATGA[A/G]GCAGTTATTGCTCAT	23077
rs149541006	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77306301	CATGTTCAAGCATCA[A/G]TGAATAAATTAGGGA	23077
rs149551259	snp	A/G	0.0150606	0.0854603	intron-variant	MYCBP2	GRCh38.p7	13:77318983	GCTAATGTCAAAACC[A/G]TGAACTACCTCAAGC	23077
rs149559115	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77106103	TCAGGACCCTGACCT[C/T]ATCTCTGGAACCACA	23077
rs149559366	snp	C/T	0.00953873	0.0683987	intron-variant	MYCBP2	GRCh38.p7	13:77195984	GCACAGTTCTAGAAA[C/T]TGGGCATAAAGGGGC	23077
rs149569279	snp	A/G	0.0146672	0.084371	intron-variant	MYCBP2	GRCh38.p7	13:77245139	TGGAGAAATAGGAAC[A/G]CTTTTACACTGTTGG	23077
rs149602238	in-del	-/C	0.0134861	0.0810011	intron-variant	MYCBP2	GRCh38.p7	13:77132663	TTCTCTTCCACTCAA[-/C]CCCCCTCACAATGTT	23077
rs149637341	snp	G/T	0.000153988	0.00877328	synonymous-codon	MYCBP2	GRCh38.p7	13:77121389	TTTGCTATTTCCGAG[G/T]CCATAATCAAATCCT	23077
rs149642504	snp	A/G	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77179827	CTTCCAGCAGTGAGA[A/G]CTATCTTTGCTTTTC	23077
rs149646035	snp	A/T	0.00676609	0.0577691	intron-variant	MYCBP2	GRCh38.p7	13:77272859	GAGAAGAGTAGACAG[A/T]CAGGTCTTAAGATCA	23077
rs149649903	snp	A/G	3.2969e-05	0.00405998	synonymous-codon	MYCBP2	GRCh38.p7	13:77068655	ATATTGCCGGCCAAC[A/G]TTAGAGCCACTCAGT	23077
rs149653485	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77057156	ACAGTTGAGTGACTG[A/G]GAGATTATTTAATGC	23077
rs149654415	snp	C/T	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77197251	AATGGAGACAGAAAG[C/T]ATAGAAAGAATATGT	23077
rs149657232	snp	G/T	9.90737e-05	0.00703754	missense	MYCBP2	GRCh38.p7	13:77088895	TGCTATTTCAAGACC[G/T]TCTAGATCATGATGT	23077
rs149658327	snp	A/G	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77322324	GTCACAATCCCCTCT[A/G]TTGTTTTCACTAACA	23077
rs149662853	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075179	TACCACTGCACTCTA[C/T]CCTGGATGACAGAGA	23077
rs149676141	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77220241	GTAGGAAATAAAGTT[-/A]AAAAAAGGGTGAAAA	23077
rs149686048	in-del	-/AAAT			intron-variant	MYCBP2	GRCh38.p7	13:77099166	AAGGAAAGAAGGGGG[-/AAAT]AAATATTTCTAATAA	23077
rs149695986	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77066444	TACTATTTAGTTCAG[C/T]TGACTTTTTTCCTAG	23077
rs149708199	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77285889	GAAAGGAAAGGAAAG[C/G]AAAGGAAAGCAAAGG	23077
rs149717702	snp	A/G	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77192081	TTTCATATTAAAATT[A/G]GAATGTTTTAAACTG	23077
rs149739688	snp	A/G	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77275710	GAATCTTGGCCAGGC[A/G]CAGTGGCTCATGCCT	23077
rs149746084	snp	C/T	0.0189856	0.0955633	intron-variant	MYCBP2	GRCh38.p7	13:77060364	AGTATACAGCACTGA[C/T]AGATTATAGGAGGAA	23077
rs149773015	in-del	-/AATATATAATATATATTATATATATTTTAAATATA	0.495596	0.0467178	intron-variant	MYCBP2	GRCh38.p7	13:77174910	ATACTATATATATAT[lengthTooLong]AATATATATTATATA	23077
rs149782128	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77218281	ACTGGCCTGTTAGAG[A/T]TCTTTATAAATAATT	23077
rs149791917	snp	A/G	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77269163	ACAGCATTAAGACAC[A/G]AAAACCCAGGGCTTT	23077
rs149798244	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77307393	TAATCCTCTATCCCT[C/T]TTCATCACTAAATTT	23077
rs149800496	snp	A/G	0.00993419	0.0697739	intron-variant	MYCBP2	GRCh38.p7	13:77144252	TACAGTGCCTGGGCG[A/G]ACACCAGAAATTATT	23077
rs149822734	snp	C/T	0.0479149	0.147179	intron-variant	MYCBP2	GRCh38.p7	13:77072102	GACCATCCTGGCTAA[C/T]GTGGTGAAACCCCAT	23077
rs149828151	snp	C/T	1.64898e-05	0.00287135	missense	MYCBP2	GRCh38.p7	13:77189019	TTTGCTGTTTGCCTT[C/T]TGAAGCACTGCCATC	23077
rs149834415	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77211490	AATAAAACCTCAAGA[C/T]GTCTAAATCCACAAC	23077
rs149836734	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77303718	TAGAATGCTGCTAAC[A/G]CAGTACTTCCACAAA	23077
rs149844885	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77086240	ATTTTCTTTCAGCAC[A/G]TTGAAAAAAACCAAC	23077
rs149853089	in-del	-/ACTA	0.0146672	0.084371	intron-variant	MYCBP2	GRCh38.p7	13:77288460	GTAAAGATTAGACAC[-/ACTA]ACTGACTTGCAGAAG	23077
rs149854402	snp	C/G	0.000230658	0.0107366	synonymous-codon	MYCBP2	GRCh38.p7	13:77139250	AAAAGAGAGGCACCA[C/G]GCTTCAGTGTAACCA	23077
rs149866153	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77242582	ATGAAAGCATAGTTA[C/T]GTGCTGAACTGGAGG	23077
rs149877885	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77157146	AGCTGGTTGCAGTGG[C/T]ACAATCACAGCAACC	23077
rs149903282	snp	A/T	3.30218e-05	0.00406323	missense	MYCBP2	GRCh38.p7	13:77098324	TGTCTGTTAGACTAT[A/T]TGTTTTTAAAGTACT	23077
rs149918096	snp	C/T	0.00557542	0.0525036	intron-variant	MYCBP2	GRCh38.p7	13:77237924	GTCAAATCAAGAAAA[C/T]CATAATGGTTTTAAG	23077
rs149956740	snp	C/T	3.30229e-05	0.0040633	synonymous-codon	MYCBP2	GRCh38.p7	13:77140095	CACTATGCCTATCTG[C/T]TCACTCTGAAGGGAA	23077
rs149960121	snp	C/T	0.00835141	0.0640778	intron-variant	MYCBP2	GRCh38.p7	13:77103377	ATTTAGCAGAGAACA[C/T]AAGCAAAAACAAAGC	23077
rs149995434	snp	A/G	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77265614	ACCTGATTTATGTCA[A/G]CTTGAAACATGGTAT	23077
rs149999848	snp	C/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77049894	ACCTGCTTCGGTCTC[C/T]CATAGTGCTGGGATT	23077
rs150005058	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77312260	ACATTAGGCTGAAAG[A/G]AAATGCTGCATCTTC	23077
rs150009936	snp	C/T	0.000594933	0.017237	synonymous-codon	MYCBP2	GRCh38.p7	13:77098463	TTTTGGTTTTGGTGA[C/T]GTTGACCGTCCTCTC	23077
rs150014334	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77186449	AAAAATAAAGCTTTT[C/T]ACAGTCACTGTAGTA	23077
rs150035176	snp	A/T	0.00557542	0.0525036	intron-variant	MYCBP2	GRCh38.p7	13:77115351	ACCAATTCTAAAAAC[A/T]ATATAATTAGTTTTT	23077
rs150047029	snp	C/T	0.00755907	0.0610114	intron-variant	MYCBP2	GRCh38.p7	13:77256315	TAATAAAAAAATGTT[C/T]GGAAAAGACTTTTCT	23077
rs150053649	in-del	-/T	0.110167	0.207236	intron-variant	MYCBP2	GRCh38.p7	13:77054410	CTAGAAGTATTAATT[-/T]AGCAGCAGTGTAAGG	23077
rs150054254	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77133454	AGTGTAATTTTTAAT[A/G]CTTAGGAAGAAACAA	23077
rs150112063	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77314856	AGGCTATGCGTGAGT[A/G]GGGGAAAGGGATAGA	23077
rs150117946	snp	C/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77100552	AGGTGACATTAGTTA[C/T]TGATGTGCAAGGGTT	23077
rs150119828	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77188559	AAGTGGTTCAACAAA[C/T]TTCCTAGTTAGATAT	23077
rs150128132	snp	C/T	0.00438332	0.0466095	intron-variant	MYCBP2	GRCh38.p7	13:77117748	AGGTTCAGGAGGTTA[C/T]TAAGAAAAAAGAACA	23077
rs150131264	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77208997	GTGCAATGCATATGA[C/T]AATTATAAAATTTAA	23077
rs150141272	snp	A/G	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77259464	AATATACAAGTTTCC[A/G]TCAGCTCTACCCAGT	23077
rs150148665	snp	A/G	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77045711	GGAAGAAGTGATGGG[A/G]TCCCTTACTCACTAT	23077
rs150152461	snp	A/G	1.64857e-05	0.00287099	synonymous-codon	MYCBP2	GRCh38.p7	13:77212077	AGTAGCTTTTCTTCC[A/G]TATTTTGATCCAATG	23077
rs150173396	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77182568	CAACATTTGCTAAAT[A/C]TAGCCTGTTCTGTAG	23077
rs150180383	snp	A/C/T			intron-variant	MYCBP2	GRCh38.p7	13:77233876	AGAGAGAGAGAGAGA[A/C/T]CGAGAGAGAGAGAGA	23077
rs150185560	snp	A/G	0.0256215	0.110247	intron-variant	MYCBP2	GRCh38.p7	13:77295043	GCAAATGGAGTTGGA[A/G]CTACTGGCAGCCTCA	23077
rs150190050	snp	A/T	0.00279162	0.0372561	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076983	ACTATTTTTCTTAAT[A/T]ACAAATGCAACATGG	23077
rs150200070	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77127919	ATAACCAATTTTTAC[C/T]TATACAAATATGTAC	23077
rs150236976	snp	A/C/T	3.2961e-05	0.00405951	missense, utr-variant-5-prime	MYCBP2	GRCh38.p7	13:77288229	ATTCTCCACTCTGCA[A/C/T]AGAGTTCTTAGATGC	23077
rs150267633	snp	C/T	0.000461255	0.0151794	missense	MYCBP2	GRCh38.p7	13:77158027	ATTTGGAGTGGTAAA[C/T]TTCCCTCAAGTGCTT	23077
rs150275330	snp	C/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77061933	TATTAAACAGAATTA[C/T]TGCAAATGTACTTAA	23077
rs150278131	snp	C/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77323593	GCCTTCACAGTTACT[C/T]ATTACTAAGTGAAAT	23077
rs150307006	snp	A/G	0.0271762	0.113356	intron-variant	MYCBP2	GRCh38.p7	13:77095954	GAAAAGAGAGAGTAG[A/G]TATGGAATAGGAAAA	23077
rs150327506	snp	A/G	0.000231076	0.0107464	missense	MYCBP2	GRCh38.p7	13:77180146	GATCCCAGGGCTGAC[A/G]CTGTCAGTTCACTGA	23077
rs150329519	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77147065	GACCTATAGCTACAC[A/G]GCTGAACCTCAAAAA	23077
rs150340001	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77164257	AGGGTGTCCATGTGC[A/G]TGTGTAAATTAAAAA	23077
rs150357286	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77089200	TTCAGAAAGATTAAA[C/T]ATGTTACTCTCTGAA	23077
rs150361011	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77175698	GGGCGCGGTGGCTCA[C/T]GCTTGTAATCCCAGA	23077
rs150361610	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77213087	GAAACATGGCAAGCA[C/G]ATGATTAGAGAAGCA	23077
rs150370405	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77229818	TAATATTTTCATCAC[A/G]CTGCACCATTTCCAA	23077
rs150378820	in-del	-/T	0.0744748	0.178019	intron-variant	MYCBP2	GRCh38.p7	13:77312825	TTGACAGTGGATTTC[-/T]TTTTTTTAAGGGCAA	23077
rs150390066	snp	A/G	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77158206	CAGATAGGCCTTTAC[A/G]GAGAAATCATTTTCT	23077
rs150393139	snp	C/G	0.0614824	0.164198	intron-variant	MYCBP2	GRCh38.p7	13:77244723	TATCATCAGAGTGAA[C/G]AGGCAACCTACAGAA	23077
rs150395648	snp	A/G	0.000182423	0.00954872	synonymous-codon	MYCBP2	GRCh38.p7	13:77097440	CAGTTCACAGATGGT[A/G]TCTTTCTCTGGTCCT	23077
rs150401246	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77121551	GCTATTCCCTATTCA[C/T]ACAACAAAGAGAGAA	23077
rs150402973	snp	A/T	0.0189856	0.0955633	intron-variant	MYCBP2	GRCh38.p7	13:77300460	ATTCTCTTCCTTTTT[A/T]ATTTTCTTTTCAACC	23077
rs150417680	in-del	-/C	0.0414363	0.137845	intron-variant	MYCBP2	GRCh38.p7	13:77132646	TTCCCTTGATATAAA[-/C]TTTCTCTTCCACTCA	23077
rs150445210	snp	C/T	0.00993419	0.0697739	intron-variant	MYCBP2	GRCh38.p7	13:77239012	ATAATCCCAGCTACT[C/T]GGGAGGCCGAGGCAG	23077
rs150447548	in-del	-/A	0.0379877	0.132479	intron-variant	MYCBP2	GRCh38.p7	13:77248691	TGGTTGGCCGCTGTG[-/A]AAAATAGTATGGCAG	23077
rs150498921	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77123252	TTCCTTATCACTCCA[C/G]GTTTTATATTAAAAT	23077
rs150502237	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77246406	GAGAACAAGAATTCA[A/T]TCTTTGAGGTCAGGA	23077
rs150522437	snp	C/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77172191	GGAGTGAGCCGCGCA[C/T]CCAGCTGACCTGAAT	23077
rs150542766	snp	A/G	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77255472	TTTCACAAGAGTTTC[A/G]GAATAAGGAAACAAT	23077
rs150582666	snp	C/T	0.00478085	0.0486577	intron-variant	MYCBP2	GRCh38.p7	13:77108922	GTTAGCCAGGATGGT[C/T]GACCTCGTGATTCAC	23077
rs150612472	snp	A/G	0.0217236	0.101931	intron-variant	MYCBP2	GRCh38.p7	13:77179482	CTTTACAAAATGTAA[A/G]GGCACTTTCAAAGTG	23077
rs150637697	snp	A/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77189968	AAATTAGTAAGAAAA[A/T]CAATGGATAGATTTT	23077
rs150644522	snp	A/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77069248	CAATTGAAAGCATCT[A/T]AGATTCAATGAAACA	23077
rs150670125	snp	A/T	1.66852e-05	0.0028883	missense	MYCBP2	GRCh38.p7	13:77263966	TTAATATATTCTCCA[A/T]CAGTGAATAAAATAT	23077
rs150679425	snp	A/G	0.0185938	0.0946107	intron-variant	MYCBP2	GRCh38.p7	13:77138139	TTCAACTTAACCTCC[A/G]TAAAGCAGTAAGCCA	23077
rs150689990	snp	C/G	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77278321	GATTATTTCTGGATT[C/G]CAGGGATTTATGTTT	23077
rs150706323	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77079146	TTCCCTCTCCTTATT[C/G]AAAGTCTAAATATTC	23077
rs150751268	in-del	-/AAAC			intron-variant	MYCBP2	GRCh38.p7	13:77303334	CGAGACTCCGTCTCA[-/AAAC]AAACAAACAAACAAA	23077
rs150759879	snp	A/G			intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77074218	ATTTATGGTAAATTG[A/G]CTATTGATAAATGAT	23077
rs150794561	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77155877	TCACAAAAAAAACAG[A/G]TGTAACTTGGACACT	23077
rs150806245	snp	A/G	0.00676609	0.0577691	intron-variant	MYCBP2	GRCh38.p7	13:77297206	AGGAAGCCCCTGAAT[A/G]ACTTTTGAGAAACAG	23077
rs150834693	snp	C/T	3.30186e-05	0.00406303	missense	MYCBP2	GRCh38.p7	13:77097811	CCTTGTTTTTGTTGA[C/T]GCTACCCATCTTAGA	23077
rs150845109	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77149755	GTGAATTTCATCTTT[C/T]ATTTCCTACCTTTCT	23077
rs150848293	snp	A/C	0.0146672	0.084371	intron-variant	MYCBP2	GRCh38.p7	13:77237831	TACTTATACTCTCTA[A/C]ATTCTTCATATAATA	23077
rs150858572	snp	C/G	0.0256215	0.110247	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77292003	CTGTCAGACTGCTCT[C/G]CATGTACGAACATCA	23077
rs150881630	snp	A/G	0.00557542	0.0525036	intron-variant	MYCBP2	GRCh38.p7	13:77307455	ACATAGCAAGACCCC[A/G]TCTCTATTAAAAAAA	23077
rs150885628	snp	C/T	1.65425e-05	0.00287593	missense	MYCBP2	GRCh38.p7	13:77257703	ATGGCACCAGTATCT[C/T]GTCCACACTGTCCTT	23077
rs150891159	snp	A/G	1.64727e-05	0.00286986	synonymous-codon	MYCBP2	GRCh38.p7	13:77067715	GCATCCTAGAAACAT[A/G]TCCAAGATACCCAGC	23077
rs150901012	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77231628	TTGGTTTTCATTTAA[C/T]GTTTCATTTAAAAAT	23077
rs150932279	snp	A/G	0.0138799	0.0821421	intron-variant	MYCBP2	GRCh38.p7	13:77100291	ACGCTCTATTTCTCT[A/G]TGGCTCAGGACAGTA	23077
rs150932342	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77200080	AAGAAGGCTTCAGAT[A/G]ATCAAATTACTCTGA	23077
rs150953735	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77115138	ATTGATGAAATGGTA[A/G]TCTTAAATACCTACA	23077
rs150955834	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77152430	ATATACTGGATAGGA[C/G]AAGGTGGTTCCCTGG	23077
rs150956935	snp	C/T	0.00557542	0.0525036	intron-variant	MYCBP2	GRCh38.p7	13:77238852	AACTAGGGCCCAGGC[C/T]GAGCGCAGTGGCTCA	23077
rs150967421	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77294677	CACCAAAAAGTTGAA[A/C]AGGGATAGAGGTTGG	23077
rs150972540	snp	A/C	1.67231e-05	0.00289159	utr-variant-3-prime	MYCBP2	GRCh38.p7	13:77045358	AATTTTTCTCTCTGT[A/C]GACAAAGGATCTGCG	23077
rs150977758	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77309366	ATACTGAACATAATG[C/T]ATCTGAACAGGACTG	23077
rs150986738	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77181314	ATTAAGTAGATATTT[A/T]AAAAATCCTTTATTT	23077
rs150994434	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77059055	TCCGCATCACCAAAA[G/T]GCAGATTTTTTTTTT	23077
rs151008732	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77233915	GGAGCTTGGGCTTTA[C/T]ATTGATGGTAAAGGG	23077
rs151027249	snp	C/T	0.00557542	0.0525036	intron-variant	MYCBP2	GRCh38.p7	13:77127805	CAAGAATTCTGTATA[C/T]CTGCTACTTTGTTAA	23077
rs151034063	snp	C/T	0.000165038	0.00908251	synonymous-codon	MYCBP2	GRCh38.p7	13:77098649	TGGAGAACTAGCACC[C/T]GATGGGCTAGACCTA	23077
rs151037137	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77173942	ATCAAGGCAACACCA[C/T]TATCTGAGTACAGTC	23077
rs151040580	snp	A/G	0.0341408	0.126114	intron-variant	MYCBP2	GRCh38.p7	13:77268694	TGAGGCAAGAGAATC[A/G]CCTGAACCTGGGAGG	23077
rs151065051	in-del	-/A	0.125182	0.216612	intron-variant	MYCBP2	GRCh38.p7	13:77314583	CTATGGAGACAGTAA[-/A]GTGATTACCTGGGGT	23077
rs151069766	snp	A/G	6.60611e-05	0.00574684	missense	MYCBP2	GRCh38.p7	13:77185937	AGGTACCCACAAAGC[A/G]CAGTCTCTCTAAATC	23077
rs151082775	snp	C/T	0.00438332	0.0466095	intron-variant	MYCBP2	GRCh38.p7	13:77210829	AATGATAATAGCAAA[C/T]ACTTATATGGCACCT	23077
rs151088212	snp	A/C/T	4.96186e-05	0.00498069	missense	MYCBP2	GRCh38.p7	13:77156134	GTAGGCCAACCACAA[A/C/T]GAATATCATCCTTAT	23077
rs151126336	snp	A/G	0.00914312	0.0669923	intron-variant	MYCBP2	GRCh38.p7	13:77250844	TCTAGCATTAAATAG[A/G]CTTTGAAAAATAATA	23077
rs151146039	snp	C/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77146593	ATATAGAGAATAAAT[C/T]CATACAAAAGAGATA	23077
rs151151149	snp	A/G	9.98486e-05	0.00706501	missense	MYCBP2	GRCh38.p7	13:77057057	TTTCTAATACTCGCC[A/G]ACAGCACTGTAAGTG	23077
rs151151673	in-del	-/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77287904	TTTTTTAATTGCCCC[-/T]ATAACAGACTCCAAC	23077
rs151156718	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77287585	AGTTCAGTTGGTTCA[C/T]AGGTGATTTTTTTTT	23077
rs151158886	in-del	-/A	0.0988943	0.199166	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77077025	TAGGGCTATGAAAAG[-/A]AAAAAATGGGCAACA	23077
rs151163687	snp	A/G	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77071259	TATATATGCATGCAC[A/G]TGTGTGCACACGCAC	23077
rs151186300	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77088013	GGTCTCAAACTCTTG[C/T]GCTCAAGTGATCCTC	23077
rs151195990	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77141588	TCAGCCTGGCCACCA[C/T]AGTGAAACCCCATCT	23077
rs151198179	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228637	AGATGTGAATAATCT[C/T]ATAATTGGCCATTTA	23077
rs151200615	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77265952	TTGGTTCATTCTTCA[C/T]CACTAATACAGCACA	23077
rs151204446	snp	C/T	0.000115532	0.0075995	missense, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77077210	TCCTCTGCTGGGCCA[C/T]ACTGGCTGAAATCTG	23077
rs151221521	snp	C/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77281987	TTTTAAAATTGTTTG[C/T]ATAAAGCAAATATTT	23077
rs151226181	in-del	-/A	0.0414363	0.137845	intron-variant	MYCBP2	GRCh38.p7	13:77168801	ATCTTTCAATTGATT[-/A]AAAAAAGATTTATCT	23077
rs151226951	snp	A/G	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77064526	TTATGTTGACTTAGT[A/G]ATTAAAATTTGTTTA	23077
rs151230999	in-del	-/AG			intron-variant	MYCBP2	GRCh38.p7	13:77233887	AGAACGAGAGAGAGA[-/AG]GAGAGAGAGAAAGGA	23077
rs151239610	snp	C/T	0.000672338	0.0183226	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77082021	TATATAAGCAATATA[C/T]GAAATAATTATTTTC	23077
rs151240012	snp	A/G	0.0115144	0.0749975	intron-variant	MYCBP2	GRCh38.p7	13:77170404	AATACTGATTCCTAG[A/G]TCTGCTGTTATATCA	23077
rs151251370	snp	C/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77221647	TAACTGCAATGCACC[C/T]TTCCCAGTTTCTATG	23077
rs151252830	snp	A/C	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77311908	AGCTCAGTACTCTTC[A/C]AAGAGGATAAACTTA	23077
rs151293153	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77166119	TTTTTTTCACAAAAT[A/C]CTTAAAACATTGTCT	23077
rs151312983	in-del	-/GCT	0.0283406	0.115616	intron-variant	MYCBP2	GRCh38.p7	13:77253615	AGTGGGGCTTTCTGG[-/GCT]GCTGGTAATATGTGG	23077
rs151327482	snp	C/G	1.66488e-05	0.00288515	missense	MYCBP2	GRCh38.p7	13:77176618	TGAGTTGAATCTCCT[C/G]CATGTTCACTCTAAA	23077
rs180699002	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77052979	TCAAAAATACAAACA[A/G]ACACAGAAATTAGCC	23077
rs180715196	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77072635	TCAAACTGATGAATC[G/T]TTAGAGAAACTATTT	23077
rs180729841	snp	C/T	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77092776	TTCTATTCAGCTTTC[C/T]GAGAAGCTCTTTACT	23077
rs180760496	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77212932	CTCCCCTCACAGCAT[C/T]CTGGAACAAGGGAGC	23077
rs180764064	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77142850	GAATTTTGAAATTTT[A/G]AATTAGGGATGCTCA	23077
rs180769249	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77173388	ATGTACTATTTATTG[C/T]AGTGCTTATGTAACA	23077
rs180769604	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77192727	ATCCTTCAATGCTCC[C/G]AATGCCTTAGGAGTC	23077
rs180774614	snp	A/G	0.0197687	0.0974348	intron-variant	MYCBP2	GRCh38.p7	13:77122639	AGCTTGCAGTGAGCC[A/G]AGATCGCGCCACTGC	23077
rs180781661	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77152075	TATTTTTAAGTAATT[A/G]AGAGCTACCTCAGAA	23077
rs180807187	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77165905	ACCATAAGTTTTAAA[A/G]CATAGTTTCTCTTCA	23077
rs180813472	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77112654	ATGTTGTCTTGGCTG[A/G]TCTCAAACTCCTGGC	23077
rs180820217	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291068	ATTGGAAAATTCAAT[A/G]TCATTAAAATGGCAA	23077
rs180826899	snp	A/T	0.00795532	0.062565	intron-variant	MYCBP2	GRCh38.p7	13:77234309	GGAATTATGACACTA[A/T]ATAAGCACTGAACAT	23077
rs180829765	snp	A/G	0.00874735	0.0655527	intron-variant	MYCBP2	GRCh38.p7	13:77271060	TTTTTCCTAATGTCT[A/G]ACTACTTTTTATATT	23077
rs180834020	snp	C/T	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77261716	AAGTCTGAAATATTT[C/T]GAGAATTACCAAAGT	23077
rs180835537	snp	C/G	0.0023928	0.0345062	intron-variant	MYCBP2	GRCh38.p7	13:77251133	ACATGTTCTTTAGTA[C/G]GAATCATTGTCTCTT	23077
rs180837792	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77223856	CATCCTGCTGCAATG[G/T]AAGCTGAGAAAGGGA	23077
rs180850480	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77183768	TGTTAGGCTGGTCTC[A/G]AACTCCTGACCTCAA	23077
rs180858435	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77244356	GATAAGTGAAGGCAG[C/G]TGTTGGTAGCCTTCA	23077
rs180862287	snp	C/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77281906	TCCTATACTTTTATA[C/T]TTGAAAAAGCTCAAA	23077
rs180864595	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77309578	CCCTTTCTATCTAGA[C/T]GAAAATCATTATTAT	23077
rs180874180	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77117059	CTTTGTTTTTCCCTT[C/T]GTCCTTACCTTTAAA	23077
rs180886215	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77208881	TTTATCTGCTCTTTA[C/T]AGATGTTGTTTCTAA	23077
rs180891963	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77201972	GACACCCTAACATCA[C/T]AATTAAAGGAACTAG	23077
rs180893432	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77256226	GCATGTGCTGTTAAA[C/T]GGGAAGATAATATAC	23077
rs180899391	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77110045	CATGAAATCAGTGCA[C/T]CTTGAAAATGAACAG	23077
rs180903775	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77097145	ATAATATTTTTTAAA[A/C]CATGCTACATGAAAG	23077
rs180909742	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77136391	CTATATTGTTCTAGG[A/C]TTTTATTAAATCTTC	23077
rs180914124	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77187768	ATGGTCTGGGAAGGC[C/T]GGGTGCGGTGGCTCA	23077
rs180920398	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77169321	GAATGGCGTGAACCC[C/G]GAAGGCGGAGCTTGC	23077
rs180925258	snp	A/C	0.00716266	0.059414	intron-variant	MYCBP2	GRCh38.p7	13:77148440	ATCAAAATAAAATGG[A/C]CTGTTCAGTTTTTTA	23077
rs180926403	snp	C/G	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77057357	TATAAAGTAAGCTAG[C/G]TTAGGAAAAAAAGTA	23077
rs180928479	snp	A/T	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77127260	AGGAGAAATTAAACA[A/T]GGATTTAAGTAAATA	23077
rs180930975	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076027	AAAGACACTAGAATA[C/T]TGAGACTAGTCAGAG	23077
rs180941318	snp	A/G	0.0471551	0.14613	intron-variant	MYCBP2	GRCh38.p7	13:77238238	ACAGAGCGAGACTCC[A/G]TCTCAAAAAAAAAAA	23077
rs180944043	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77196736	GTTTAGGCAGATCAT[C/T]AGAAGCATAGTATTG	23077
rs180955187	snp	A/G			intron-variant, downstream-variant-500B	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77088153	ATAATTTGGGGTTTT[A/G]ATTTAAAAAAAACAG	23077
rs180961554	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77294687	TTGAAAAGGGATAGA[G/T]GTTGGAATGACTGTA	23077
rs180962190	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77156910	CTCCAATCACTATTT[C/T]GTGATTTTTAAAAAC	23077
rs180968374	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77306675	AGGTAGGCCAGGGAA[A/C]CTCAAGCCTTGAAGC	23077
rs180969524	snp	G/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77314440	ATTATTCAGTGGTAA[G/T]AAATGAGCTATCAAG	23077
rs180970749	snp	C/T	0.00636936	0.0560724	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228766	CAGTAGCTACAAAGC[C/T]TTGGCAACTATGTAA	23077
rs180973479	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77217087	GATATTCTACACACT[G/T]TTCTTAGTTGTGCAA	23077
rs180975153	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77247655	AGTACTCGGTTTTGA[C/T]TTCAAAACTTACTAC	23077
rs180983942	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77069361	GGTGCCGTGGCTCAC[A/G]CCTGTAATCCCAGCA	23077
rs180996797	snp	A/G	4.95569e-05	0.00497755	synonymous-codon	MYCBP2	GRCh38.p7	13:77176539	GATCTCAGCTATATC[A/G]CTGGGTGAGTCATCC	23077
rs181009697	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77286927	TCTAGCTCTGTTGTC[C/G]AGGCTGGAGTGCAGT	23077
rs181011399	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77328382	ACAAAGGACAAGACA[C/T]GTGGAATCATAGTAT	23077
rs181021878	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77266872	GGACATGAAATGTCA[C/T]ATTTACTTTAACATA	23077
rs181084304	snp	C/T	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77239365	TGTATGTATGGCAGC[C/T]GGAACACTAACATTT	23077
rs181094373	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77197965	GCCTCCATAATTCTA[G/T]ATACTACAGTGTTTG	23077
rs181098488	snp	C/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77218684	TACTTGGATCAGCGT[C/G]TGGCACACAGTTAAC	23077
rs181102514	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77286247	TACACAATCCCTTGT[A/G]GATATGTATAAGCTT	23077
rs181104006	snp	A/G	0.00557542	0.0525036	intron-variant	MYCBP2	GRCh38.p7	13:77246935	CCTTTCATAATAAAA[A/G]CAGTAGACAAACTAG	23077
rs181107282	snp	C/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77179124	AATGAAATTCTAAAG[C/G]CTAAACTGTCACAAT	23077
rs181111042	snp	C/T	0.00478085	0.0486577	intron-variant	MYCBP2	GRCh38.p7	13:77265583	AGACAAGCTGGAACA[C/T]GAAGCTCAAGGAATT	23077
rs181118755	snp	C/G	0.00755907	0.0610114	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77227316	TCTAATGTGGGTTTG[C/G]CAAATTAAATCAAAG	23077
rs181126101	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77187578	AATTAGAATAATGGT[A/T]CGCAAACGGAGAAGA	23077
rs181134267	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77208518	TTGGTATACCCAGAC[A/T]ACAGAATTCCACAAT	23077
rs181137904	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77315820	GACTTGCTGGATCCC[A/G]GGAGGCAGAGGCTTC	23077
rs181149982	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77052126	TAAAGCTATTTCTTC[C/T]TTTTCTTTCTTCCCC	23077
rs181154024	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77277887	TAGTTAGCATCGGAG[A/G]AAAAAAGCAATTAAC	23077
rs181160152	snp	A/G	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77304435	AAAAAAGTTGATCTC[A/G]TAAAAGTAGAAAGTA	23077
rs181165441	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77257062	AACCATAAAAAACAC[G/T]GAGATCCTATCATTT	23077
rs181168875	snp	C/T	0.00199481	0.0315187	upstream-variant-2KB, intron-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77327261	TCCGGGTTTTACTGG[C/T]AGCTTGAAGAAGAGT	23077
rs181274913	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77069111	CTTACAGTTTAGCAC[A/G]TCAAAAACCAATCAC	23077
rs181281684	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77088025	TTGCGCTCAAGTGAT[C/T]CTCCCTCCTCCGCCT	23077
rs181301295	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77321797	TTGCACTTCCAGATA[A/G]ACAGTAAACTCAAGT	23077
rs181302884	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77302034	AAACAAAAATGGGAT[A/G]AACCAAACAGAGAAC	23077
rs181329947	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77147603	AAATGAATTAGAAAT[A/G]ATCTAGCTGACTTTA	23077
rs181342108	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77126092	AATACCAAACATTTA[C/T]ATATACAATACAAAT	23077
rs181348715	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77109822	TTAATACTTTTATAA[G/T]TTCTTACACCTGTTT	23077
rs181356351	snp	C/G	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77047165	TGAGAAATAAAAATA[C/G]TGAAAACACACCTGC	23077
rs181371889	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77046926	GGTGGGGGAGAGTGC[A/G]CAGGATGGGGACACT	23077
rs181425854	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77169183	GGAGGGCGAGGCGGG[C/T]GGATCACGAGGTCAG	23077
rs181443033	snp	A/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77056928	TATGTTTATTTTGAA[A/T]GGTGAAAAGAAAGAA	23077
rs181475522	snp	A/C	0.00140697	0.026486	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076700	TGAATTATTTCACTG[A/C]AAAAAAGAATAAAAA	23077
rs181488425	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77067456	CTTTTTAGATATTAG[C/T]CAGTTGTTTATGGAT	23077
rs181522054	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77109169	GTTCTCTAACACAAT[A/G]GTCCCCTAACTTTCT	23077
rs181525083	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77178355	ATTCTGCAGAGATAG[C/G]TGTGCAAGGAAGAGG	23077
rs181526966	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77197509	CTTTAACATATTTAC[A/G]TGAAAATGCATCAAA	23077
rs181539027	snp	A/C	0.00592509	0.0541058	intron-variant	MYCBP2	GRCh38.p7	13:77157916	CCCTAAAATAAAGTA[A/C]GTAACTTAAAGTACA	23077
rs181539878	snp	A/G	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77137125	ACTCCACTCCTTACC[A/G]CTCCTCTAACCTTTG	23077
rs181545918	snp	C/T	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77117870	ACTGGAATCAAATGA[C/T]CAATTTAACATATTA	23077
rs181551745	snp	C/T	4.95242e-05	0.0049759	missense	MYCBP2	GRCh38.p7	13:77098509	GGCATTTTCTTCTTG[C/T]GGAGGGTATCTGGAT	23077
rs181566243	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77131264	GTGCATGCCTATACT[C/T]GTAGCTATTCAGAAG	23077
rs181571986	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77112431	TATTATATCTGTATA[C/T]ATACATATTAGAGAC	23077
rs181576351	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77092282	ACTGAAATCTTCATG[A/T]CATCTTAAACTTATC	23077
rs181584919	snp	A/G	0.00914312	0.0669923	intron-variant	MYCBP2	GRCh38.p7	13:77072208	AGGCAGGAGAATGGC[A/G]TGAACCCAGGAGTCA	23077
rs181626627	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087216	TACAGACATGGAAAC[C/T]GAGGCCTACAAGTCA	23077
rs181631916	snp	C/T	0.0189856	0.0955633	intron-variant	MYCBP2	GRCh38.p7	13:77058902	AGGCAGGAGAATCGC[C/T]TGAACCCGGGAGGCG	23077
rs181639141	snp	A/C	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77223415	TAATAAATTCTTTGC[A/C]TATCTAATCCTGTCT	23077
rs181644630	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77125577	AATCATTCCAATACA[C/T]TTCTACTAAGAAATT	23077
rs181649618	snp	C/T	0.00874735	0.0655527	intron-variant	MYCBP2	GRCh38.p7	13:77243673	CATATTGTCAGTTAC[C/T]GTAAAAGCAGTATTG	23077
rs181652114	snp	C/G	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77201458	GGGAGACTTTAACAC[C/G]CCACTGTCAACATCA	23077
rs181672795	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77187099	ATAGGCGTGAGCCAA[C/T]GTGCTAAGCCCTATA	23077
rs181681242	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77321626	CACCTGCATTCTAGC[G/T]CTAACAGAATTCCTA	23077
rs181683754	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77146246	ACCAGTCTGAACAAT[C/T]GTAAAATCATTTAAA	23077
rs181700596	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77295596	GTAGGAAACAATTGC[C/T]TCTATAGTTGCTATA	23077
rs181709290	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77300839	GAAGCAATGAGGACT[A/G]AAAGAACAAAAAATC	23077
rs181712302	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77260219	CCCTTGCCAAGCTCT[A/G]TGATTAGCTTTGCAT	23077
rs181713295	snp	C/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77256700	TCTCTCCCCAGTTAA[C/T]GTGGCTTTTATCCAA	23077
rs181717848	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77281358	TTTAGAAAAATGTTC[G/T]GATTTTTCAAATCAT	23077
rs181720505	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77217600	CTGAAATAAACATGT[A/C]CAATTCTAACAAAGC	23077
rs181724275	snp	C/T	0.00557542	0.0525036	intron-variant	MYCBP2	GRCh38.p7	13:77251544	ACTCTCCCCATTTCA[C/T]TTCTGCAAAAGAAGG	23077
rs181725290	snp	C/T	0.00636936	0.0560724	intron-variant	MYCBP2	GRCh38.p7	13:77122505	AGGAGATCGAGACCA[C/T]GGTGAAACCCCTTCT	23077
rs181769056	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77168983	TATCCTTTAACATTG[C/T]TATTGTTATTAATGA	23077
rs181787156	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291384	TACCATATGTTTGCA[A/G]AGATATGAAGCAACT	23077
rs181787938	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77277147	AGGAAAGAAATAACA[C/T]GTTCAAAGTAGGAAA	23077
rs181791832	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77271407	CTGCTTTAAACTCTC[C/T]GTTAAGCTTTATGAA	23077
rs181799234	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77083283	ACTTAAAAAATGGTC[A/G]TGTAACAGAAATACA	23077
rs181799710	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77310105	AACGGAGTGAGACTC[C/T]GTCTCAGAAAAACAG	23077
rs181804737	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77221818	TCCCTCAGCATCCAT[A/G]GGGAATTGGTTCCAG	23077
rs181812090	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77163895	TTCTCTCCTCTTCAC[C/T]GACTGTTCCTTCACA	23077
rs181830553	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77273078	AACCAATCAAAAATA[C/T]ATCAGATTGATACCA	23077
rs181837906	snp	C/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77238671	CTAGACTATTAATAA[C/T]ACAAAGATTTAAAAT	23077
rs181846509	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77310767	ACACACAGAGACACA[C/G]ACGTGTGTGCGTGCG	23077
rs181905579	snp	C/G	0.00318978	0.0398085	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77329016	GGGAAATAGATGTTG[C/G]CTGAATGAATGAATG	23077
rs181909702	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77307541	TGAGGTGGGAAGATC[A/G]CTTTGGTCCAGGAGT	23077
rs181934003	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77104133	AAAGTTTTTAACTCA[A/T]AGCAATTAAAATTAA	23077
rs181939077	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77242940	GTTATCAGAATATTG[C/T]TAATTTTAATTTTGA	23077
rs181942813	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77213539	GGGATATATTCTGCT[C/T]TTGGAGGAAAAATAA	23077
rs182001315	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77053904	TACTAGAGATAGAAA[A/G]ATGAAAAAACATACT	23077
rs182044736	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77182755	ATGACAATGATTTTT[C/T]TCACGAAGGAGGGCG	23077
rs182046412	snp	A/G	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77064513	GGTTAAAAAATAATT[A/G]TGTTGACTTAGTGAT	23077
rs182054489	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77162411	TCCTTTATTAGTTAA[A/T]ATAGAACATATTTTA	23077
rs182065858	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77183266	AATTAGTTGGGAAGT[C/G]TTGCCTCCTGTATTT	23077
rs182075353	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77142014	TCAGCTTCATTCCAA[A/G]AAACAAATATAAGTG	23077
rs182079278	snp	A/G	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77065015	TTACTCTCACATCTG[A/G]TAAAAACATAACAGA	23077
rs182081990	snp	C/T	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77122352	TATCTCAAGTATATT[C/T]TTAAATATCTTATTT	23077
rs182085393	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77103483	TTTCTCTAAAACTGA[A/G]AACAAAGGTCGAATT	23077
rs182089488	snp	A/C	0.00478085	0.0486577	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77082937	AGGGATTCTATCTTA[A/C]TATTTAAAGAGCTTT	23077
rs182105105	snp	A/G	0.00478085	0.0486577	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291661	AATCCCAGCTCCTCG[A/G]GAGCCTGAGGCAGGA	23077
rs182115926	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77252647	ATCACATCCATTTAA[C/T]ATACAGCTATCACTC	23077
rs182145228	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77105261	TGTGAAAAACTATGA[C/G]GAAACTTATAAGATG	23077
rs182169955	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77083890	CAATTTCTATTACCA[A/G]TTTCTTGGACTGTCT	23077
rs182208428	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77078437	CTGCAGTGTTATAAG[C/T]GTTATAACAGACAGA	23077
rs182213916	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77234924	ATCACACCCACACCC[A/G]TTTAATGTCTTGCTA	23077
rs182220369	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77193375	TATCTTGTACAAGCA[A/G]AGTCAGTATCTTACG	23077
rs182254304	snp	A/G	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77236261	TCTTTCATTGGGAGA[A/G]GAGTGAGTAAAATAG	23077
rs182264633	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77119447	AAAGAACTGTGTACA[C/T]GAGCCATATATCTTT	23077
rs182269521	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77195249	TTCTATACCTTCTTC[C/T]TGCCTTCTCTGTTCT	23077
rs182271665	snp	G/T	0.0138799	0.0821421	intron-variant	MYCBP2	GRCh38.p7	13:77100164	GGTAGATTTGTTAAC[G/T]GGCTATAACTGCATG	23077
rs182276136	snp	C/T	3.42442e-05	0.00413775	intron-variant	MYCBP2	GRCh38.p7	13:77061333	GAACAGGGAAAAATA[C/T]GCTTATTTATCACTC	23077
rs182276397	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77214883	GAACACCTTAGCATA[C/T]GCAGTCCATCACTGA	23077
rs182284025	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77174812	CTTGTTCAAAGTCAC[A/G]CAGCTAGTAAGTGAT	23077
rs182293667	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77132021	AGCAAAATGATGAAA[C/T]GACTCAGGAAAATTA	23077
rs182328850	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77063792	AAATAATGCATGCAA[C/G]GAGGAAGGGGAATGC	23077
rs182382111	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77230942	TTCAAATTAGGGATG[C/T]TCAACATGTCGTAAA	23077
rs182398408	snp	G/T	0.00438332	0.0466095	intron-variant	MYCBP2	GRCh38.p7	13:77248706	AAAAATAGTATGGCA[G/T]TTCCTCAAAAGATTA	23077
rs182406248	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77278458	TACCCCTGCTGTTTC[C/T]GTACCACAATTAAAT	23077
rs182408539	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77210286	CAAATTCCGCCTCCC[A/G]GGTTCACGCCATTCT	23077
rs182415560	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77171969	GCAGTGGCATGATCT[C/T]GGCTCACTGCAACCT	23077
rs182416756	snp	A/G	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77190730	AAATCATACAGTCCA[A/G]GGTCAAAGTAGTCAC	23077
rs182425705	snp	A/G	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77314756	CTAATGTAAACTCTG[A/G]ACTTGAGAGTGATTA	23077
rs182465543	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77298619	CCTTACTCAGAGATT[A/G]AAATAAGGTATCTAC	23077
rs182469799	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77269021	ACTGTATGGAAAAAA[A/G]TATTTCTAGTCCCTC	23077
rs182471572	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77317210	ACTCATCTCGGCCTC[C/T]CAAAGTGCTGGGATT	23077
rs182476388	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77297252	AAAGAATAAGAATTA[C/T]GGTGCAAGAAACAAG	23077
rs182477546	snp	A/G	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77319993	GGGGCAGTGAAAGAC[A/G]TAAGACTGAACAGAG	23077
rs182485031	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77114697	GTCTTTTGACATATA[A/T]CATATATTTCATGTT	23077
rs182489848	snp	A/G	0.00835141	0.0640778	intron-variant	MYCBP2	GRCh38.p7	13:77289638	AAGATTGTGATCCAG[A/G]CAAATTGGTCTACTC	23077
rs182510252	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77170488	TGGGGATAAATCTAA[C/T]AGTCTTTATTTTCAG	23077
rs182514154	snp	A/G	0.00874735	0.0655527	intron-variant	MYCBP2	GRCh38.p7	13:77150169	AGAGCTAAAAATCCC[A/G]AAGAGTTCTAGGAGA	23077
rs182531389	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77110684	AATATGTGATGTCAC[C/T]GCCAGAGGCCCAGCT	23077
rs182546728	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77074694	AAAGAATGAACCATG[A/G]CTACATGCTACAACA	23077
rs182554387	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77152467	CCCCACTCTCAAGCC[G/T]GGAAACCATGACCCT	23077
rs182562792	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77154009	GCATTTTGGAACTCA[C/T]TGAAATATTAGCTGC	23077
rs182570981	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77113109	ATACTTTGTGATTCA[C/T]TGGATCTCTGTAATG	23077
rs182602625	snp	A/G	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77324773	ATACACAGAAATCAT[A/G]TTACACTAGTAGTAG	23077
rs182629212	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77158986	TTTTTGGAGAGACTT[C/G]TTTTAAATGCTGGAA	23077
rs182642337	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77048247	CAGCAAGAAAGTGCC[A/G]CCTATGAGGCTGAGA	23077
rs182702279	snp	C/T	0.000224488	0.0105921	intron-variant	MYCBP2	GRCh38.p7	13:77273709	TATTCATCCAACATA[C/T]GGAACATTATATGCG	23077
rs182707970	snp	A/G	0.00438332	0.0466095	intron-variant	MYCBP2	GRCh38.p7	13:77240568	GGCCAAGATTGTGCA[A/G]CTGCACTCCAGCCTG	23077
rs182711943	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77253666	GATTACATGAATACA[A/G]TCAATTTGAGAAAAT	23077
rs182717490	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77198232	CAAGAGTCCTAATCA[C/T]TATTCTATCACTATA	23077
rs182717911	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77292339	GTGAGATTTATGAGT[C/T]CTTCTGGCAAATCAA	23077
rs182726550	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77307834	TTACATCCCTGCCCC[C/T]TGTCCCGCCAGCTTC	23077
rs182733995	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77133669	TATTCTCCCCAGTAC[A/G]TATCTGTTTTCCACC	23077
rs182751309	snp	C/G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77093943	TGTTAGCATTTTTCA[C/G/T]GTTTTACAATTTGAT	23077
rs182796336	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77049722	CTCACTGCAACCTCC[A/G]CCTCTCAGGCTCAAG	23077
rs182800643	snp	C/T	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77070251	CACATTCTGCAGGAC[C/T]TATAAAAGGGCGAGC	23077
rs182803451	snp	C/T	0.00557542	0.0525036	intron-variant	MYCBP2	GRCh38.p7	13:77101936	AATCTTCAGACTATA[C/T]GTAATACTTTCACAT	23077
rs182808730	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77054969	TCCAAATGTCTGGTA[C/T]GCAGTTGGTTATTTG	23077
rs182809723	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77090540	GCTCCTTTTAGAATC[A/G]AAAGCACTGGGGTGG	23077
rs182815893	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77138626	ATCTTGTGAACACTG[C/G]CTCTATTCTACTATA	23077
rs182820627	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77288456	AAAAGTAAAGATTAG[A/G]CACACTAACTGACTT	23077
rs182845892	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77248104	TATGTAACTAACCTG[A/C]ACGTTGCGCACATGT	23077
rs182850368	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77248659	AACATCTGTACACTA[C/T]TGGTGGGAATGTAAA	23077
rs182856703	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77219983	CAAATAGTTCAATAC[C/T]ACACAACAGGAGGAT	23077
rs182858558	snp	A/G	6.66078e-05	0.00577057	intron-variant	MYCBP2	GRCh38.p7	13:77267813	CTTAAAATTGCTTGT[A/G]GAGAAAAAATGACTA	23077
rs182860291	snp	A/G	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77181129	ATTCCAACCCCTACC[A/G]GTAGAAAAATTTCAA	23077
rs182860608	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77230149	GATGAATTCTGACCT[C/T]CTCTGAATTTTCTCC	23077
rs182863544	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77198757	ATCTCTCACTCCTCC[C/T]GGTCTCCACTCCTGG	23077
rs182866187	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77159943	CTTAAGGTACAAAGA[C/T]TTAACTTTAAAAAAG	23077
rs182881705	snp	C/T	0.00874735	0.0655527	intron-variant	MYCBP2	GRCh38.p7	13:77139620	CAGTAAAATCAGATG[C/T]TTCCCAAAGGAATAT	23077
rs182886502	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77119910	CATGCTATTTTTGAA[C/T]GATATTCACAAAATC	23077
rs182906390	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77180532	AGTACCATACATTTA[C/T]GAAATGTTTTTATTA	23077
rs182924392	snp	A/C	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77139057	TCATTACACAGAAGC[A/C]CTTAAGAATTCAAGA	23077
rs182968852	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77257309	ATTAGATACAAGAGA[G/T]CTACTATTTGATAGC	23077
rs182973095	snp	C/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77219174	GACCGAGGAAGAACA[C/G]CTCACAGACATCTAG	23077
rs182976724	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77263048	AAACTAAAACTCTCA[A/G]GAGAACTCATGATCC	23077
rs182982988	snp	C/T	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77225105	ATCACTGAACATTAA[C/T]AAAATATGGGAACAT	23077
rs182991407	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77048895	CTTCCTTATTTTTAG[C/T]ATTCTTATTTCTGTT	23077
rs182991887	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77245453	AGTTCGTGTTCTTTG[C/T]AGGGACATGAATGAA	23077
rs183001190	snp	C/T	0.223522	0.248594	intron-variant	MYCBP2	GRCh38.p7	13:77069689	GTGAAACCCCGTCTG[C/T]ACTAAAAAAAAAAAA	23077
rs183014282	snp	C/T	1.66729e-05	0.00288724	intron-variant	MYCBP2	GRCh38.p7	13:77263892	TAAGGAAAAGGAATT[C/T]CATTTACACTAGCTA	23077
rs183021518	snp	C/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77303203	CCGGGCGTGGTGGCA[C/T]GCACCTGTAATCCCA	23077
rs183047146	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77283330	TTTCTCTAACGTGTT[C/G]CACTATATCTAGCAC	23077
rs183049451	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77225320	CAGATTTGAGAGACT[G/T]CCACGCTACAGCTTT	23077
rs183052858	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77189845	TCCAACTCATTTTAT[C/T]AGTCTTATGAGACTA	23077
rs183054442	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77322625	GTGCGGACATAATGT[C/T]CTTTTGATAACACTA	23077
rs183060736	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77303026	AAAACAGCACTGACA[C/T]AGAAAAACTTGAAAA	23077
rs183066274	snp	A/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77203573	ATGGAACCAAAAAAG[A/T]GCCCGCAAGACCAAG	23077
rs183070233	snp	G/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77224678	CAAATTTGTATTTAA[G/T]GAGAAATTAATTTTA	23077
rs183071664	snp	A/G	0.00557542	0.0525036	intron-variant	MYCBP2	GRCh38.p7	13:77184262	TGCTTACTTAGAAGT[A/G]CTGTCATTTTCCAAA	23077
rs183087997	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77114955	ATATAGTTTTTCAGT[A/T]GGATAATCTTGCTTA	23077
rs183088018	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77166191	CCTTATTTATTCCTC[A/G]AATGCAATCCAGATA	23077
rs183088769	snp	A/C	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77193733	AATATATTCTAGCAG[A/C]ATGATGTCAGAGTAC	23077
rs183090961	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77143930	AGGACCACCATTATA[C/T]ACGCTGTTCGTCACT	23077
rs183093605	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77152893	ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA	23077
rs183095375	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77095057	TACACTTCAGCATTT[C/T]GCACTAACAGAGTGA	23077
rs183099459	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77123419	TTGAAAGAAGCTTCT[A/G]TCTTCTAAGTTTATA	23077
rs183101643	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77132713	AGAGTACCCAAAGAA[A/T]TGGGTGTGTAAGTTT	23077
rs183105162	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77054107	AGCCCGAGGTATGAC[A/G]AGACAGATTAGGCTC	23077
rs183110821	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77114335	TTAAGTATTTGCATC[A/C]AAAGGCAATAATAAC	23077
rs183114714	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77158504	CAGGAGTACAGTGGT[A/G]CCATCATAGCTCATT	23077
rs183115781	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77073793	CAATAGCTTTACAAA[C/T]GTTAAATGTTTAGGA	23077
rs183117746	snp	A/G			downstream-variant-500B	MYCBP2	GRCh38.p7	13:77044278	TGAGGCTGGAGGATC[A/G]CTTGAGCCCAGTTGG	23077
rs183119087	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77093594	TCTTCCAGTGTTTTG[C/G]TGAATAAGCCCACCA	23077
rs183122531	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77060765	CATAAAATCATACAA[C/T]CTTATAATAAATAGA	23077
rs183129838	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77268322	AGCATAGTGGTTTCA[A/G]AAGGTGTGGTATGCC	23077
rs183134081	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77307698	TTACTATCAAACTCA[G/T]GCAAGTCTATGAGAC	23077
rs183151597	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77245153	CGCTTTTACACTGTT[A/G]GTGGGAGTGTAAATT	23077
rs183170144	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77230477	TTGAAATGCTTGGGA[C/T]CAGAAGTGTTTTGGA	23077
rs183179908	snp	C/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77099252	AAACAACAGGTTGAA[C/T]AAATCCAGTGTGAAC	23077
rs183269179	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77287504	CAATACATGCTTCTA[C/T]TATAGAAATACCAAC	23077
rs183280011	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77283876	GCACTCCAGCCCCAG[G/T]GACAGAGCCAGACCC	23077
rs183282142	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77312441	CAACTATAACATAAA[G/T]GTCTCTGGGGGAGGG	23077
rs183299303	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77246090	TCACATATTTTGTAG[A/G]AGGTATAGCTTTAAT	23077
rs183309722	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77313406	AGAAAATTAAGAAAG[A/C]CAAAAGTTGGTTCTT	23077
rs183328101	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77149539	TGACTTCATAAGTAA[C/T]GTAAGTGCTAATGAT	23077
rs183348978	snp	C/T	0.00597247	0.0543191	intron-variant	MYCBP2	GRCh38.p7	13:77110149	AGCCACATTTTTCTT[C/T]TTACAGAGAGCCTAT	23077
rs183393422	snp	A/T	0.00119737	0.0244387	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77077019	AGGTGTTTAGGGCTA[A/T]GAAAAGAAAAAATGG	23077
rs183414062	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77188325	CACATTCAGATGGTG[C/T]CTTACAGTTCCAAAA	23077
rs183418215	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77106475	TTCAGGAGGCTAGGC[A/G]TCTAATCACAATGCA	23077
rs183420850	snp	A/G	0.000200918	0.0100209	synonymous-codon, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77078881	GAAGGTCATTGAGGT[A/G]ACTTTATTCTGAAAT	23077
rs183425859	snp	A/C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77118718	ACCAAATCTTATATA[A/C/G]AAGCCCACCTATAAA	23077
rs183445681	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77085276	TATCTAATTCTTATA[C/T]ACTAGCAATAAAGAC	23077
rs183483027	snp	C/G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291192	CTGGCAATTCAATAA[C/G/T]AAGAAGACAATTACA	23077
rs183492377	snp	A/C	0.00874735	0.0655527	intron-variant	MYCBP2	GRCh38.p7	13:77309853	GCGCAGTGGCTCACG[A/C]CTGTAATCTCAGTAC	23077
rs183503241	snp	C/G	0.00438332	0.0466095	intron-variant	MYCBP2	GRCh38.p7	13:77124374	CCAAATTGCCTCTTG[C/G]AATAATAAGTATTAT	23077
rs183509364	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77200025	TCCTCACCAGCAACG[A/G]AACAAAGCTGGATGG	23077
rs183568404	snp	A/G	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77236022	GTTTTAAACAGAGAA[A/G]TGCTACTGATCTGAT	23077
rs183576153	snp	A/C	0.00438332	0.0466095	intron-variant	MYCBP2	GRCh38.p7	13:77205060	TAATAATAATAAATA[A/C]ATAAATTTAAAAAAT	23077
rs183580898	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77128297	CATAGTTGGAAGGGG[A/C]AAGTTTTAATCCCAC	23077
rs183585359	snp	A/C	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77166674	CAACAGGATAAAGTA[A/C]AAAATTAAAATAGAA	23077
rs183592968	snp	A/G	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77088774	TGGCATCGTGAAATA[A/G]AATCATCACATGATT	23077
rs183642171	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77175070	AAGCAATCCTCCCAC[C/T]GGTGTGTTCCATCAC	23077
rs183650084	snp	A/G	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77061882	TTACAAAAATAAACC[A/G]TTATTCGGAAGTCTA	23077
rs183659408	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77209606	GACCATTCTAACTTT[A/G]GTTCTTAATACCTCA	23077
rs183660342	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77135136	GAAAAGGTTGAAGAG[A/G]TAGACACAAACAGTG	23077
rs183677654	snp	C/G/T	0.000101087	0.00710877	intron-variant	MYCBP2	GRCh38.p7	13:77169725	ATCAGCTAAAAAAAG[C/G/T]CATAAAAGGCATTAA	23077
rs183687404	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77066311	TCTGTTTGCACATTA[G/T]TTCTGTGTGCATCTT	23077
rs183711400	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77254488	AAAATATTCCTTTAC[A/G]TTCGTTTTAAATTGA	23077
rs183712042	snp	A/C			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076646	ATATGAACTGCATAA[A/C]ACTGTTATTACATAT	23077
rs183717040	snp	C/T	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77322299	GGTTAAGTTTAGATT[C/T]CCCATTTTGGTCACA	23077
rs183721941	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77214963	TATAGGTATATATAT[A/G]TAAAATAGTGTGTCT	23077
rs183738420	snp	A/G	0.00914312	0.0669923	intron-variant	MYCBP2	GRCh38.p7	13:77282279	GCCAGGCATGGTGGC[A/G]CATGCCTGTAATCCC	23077
rs183749182	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77167237	TTTATGTATATACAT[A/G]TATAAATATAACATG	23077
rs183763961	snp	C/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77045663	AAAGTAAAAAATGTT[C/G]ACTATAAAAAATTCA	23077
rs183764158	snp	G/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77144953	TATTCCCTCAACATT[G/T]TTATGCTGCAATCAC	23077
rs183764659	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77271310	TTTATTTGCAGAAAG[C/G]CTTTGAAGTCAAGAG	23077
rs183765853	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77320628	CTTGTTCTTTACAAA[C/T]GGAAAAAGCATACAT	23077
rs183768560	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77124647	GTATGAAGAAATAAA[A/C]ATGAACTTCACTATG	23077
rs183771372	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77066679	ATTTAAAATATAGTT[A/C]GATATTATAAACAGA	23077
rs183773062	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77107661	GAGGATCACTAGAGC[C/T]TGGGAGAGGGAGGTT	23077
rs183774117	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77086017	TTACAGTATTAGGTA[A/G]ATACATATCCAGGAT	23077
rs183803229	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77214206	CAATTCTGTGGAAAC[A/G]GGCAATCTCATACAC	23077
rs183804211	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77112545	ATTTGCCTGCTTCAG[C/T]CTCTCAAGTAGCTAG	23077
rs183809060	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77184572	CCTAGTTCCTCTATT[A/C]ATTACTGAAAGAGGA	23077
rs183811379	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77092487	TGGAGTTCAGTGGTG[C/T]AATCTCAGCTCACTG	23077
rs183830201	snp	C/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77063643	TAAGCTTCAGTTTTA[C/T]ATAGAATGATATATC	23077
rs183834837	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77082676	TTTTCCCCAAGATTC[C/T]TTTCAAGTCAAAACT	23077
rs183851426	snp	A/C	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77258783	TGCTTTGAGACCTTA[A/C]ATGATGTGCTAAGCA	23077
rs183860153	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77220943	TCTTTCAGTTACCAC[C/T]CAATGGAACAAGGAC	23077
rs183866036	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77241283	ATATACTATACCTAG[A/G]GAAGAATAGCTTTTT	23077
rs183867923	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77192336	TGAAAATAATATCCT[G/T]CTCATAGAGTTGTCC	23077
rs183868012	snp	A/C	0.00835141	0.0640778	intron-variant	MYCBP2	GRCh38.p7	13:77199074	AGCTCCGGTCTACAG[A/C]TCCCAGCGTGAGCAA	23077
rs183871147	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77154549	ATAAAAGGTGCAAAG[G/T]AGAAAACACAAGAAA	23077
rs183873748	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77173105	AGTCCAGGGCTCAGA[A/G]GTCATGAAGGCTAGG	23077
rs183874006	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77072231	AGGAGTCAGAGCTTG[C/T]AGTGAGCCGAGATTG	23077
rs183875227	snp	C/T	0.00874735	0.0655527	intron-variant	MYCBP2	GRCh38.p7	13:77151807	AATACTTTTTAGAAA[C/T]ATTTCCCAGAAATTA	23077
rs183886093	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77131542	CACACACACACACAC[A/T]TGAATAGTGTTCTTT	23077
rs183888895	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77297898	CCACCACCTCTTACC[G/T]GGACCACTGCAAAAG	23077
rs183903557	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77141537	GCACTTTGGGAGGCC[A/G]GGGCAGGCGGATCAC	23077
rs183909040	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77302179	CCAAAAGTGAAGAAA[C/G]AAATCAACTGAGAGA	23077
rs183914027	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77258120	GGTAATACCTCTCCA[C/T]AGTACTTTCAAACTT	23077
rs183922088	snp	G/T	0.00874735	0.0655527	intron-variant	MYCBP2	GRCh38.p7	13:77121839	ATACAAGAGTATTTT[G/T]CAAAACAAAATGGAT	23077
rs183928249	snp	C/T	4.94328e-05	0.00497131	missense	MYCBP2	GRCh38.p7	13:77150759	GTTATGGCAATATAT[C/T]GAGCTTCCTTCACTA	23077
rs183928296	snp	A/G	0.000399281	0.0141238	intron-variant, missense	MYCBP2	GRCh38.p7	13:77103248	AGAGAGCAGAGGCAG[A/G]CCCAGCTACACCATA	23077
rs183932652	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77261824	AAACCTTCAATTTGT[A/T]AAAAGAGCAATTATT	23077
rs183939236	snp	A/G	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77236628	TAAATGGAATAATAC[A/G]CAGCCATTAAAATGA	23077
rs183941222	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77195569	ATCACTGCACTCCAG[C/T]GTGGGCTACCAAAGA	23077
rs183989687	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77255743	ACACACACAGACACA[C/T]GAATAAGGCAAAGAC	23077
rs183996742	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77275858	GCATTGTGGAACGCG[C/T]CTGTAGTCCAAGCTA	23077
rs184003002	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77238018	GGAGGCCAAGGCAGG[C/T]GGATTACAAGGTCAG	23077
rs184016238	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77196662	GAGGAAACAGAAGAA[C/T]GAAGTTAACTCCATG	23077
rs184019248	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77216259	ATACCAATAATAAGT[A/G]GAAAAACAAGTAAAC	23077
rs184033131	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77065543	GTAACTCCCTGTCCT[C/T]CACACTCCCAGATCT	23077
rs184062877	snp	A/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77294347	ATCTTTGTATCCCAA[A/T]CATCCAGCATAATGC	23077
rs184068335	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77318352	AAACAGTAGTGTTTA[G/T]TAAGTAGTTAGATCC	23077
rs184079621	snp	A/C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77314257	TAAAAACATACAATG[A/C/T]CATTTGTCAATTTCT	23077
rs184092057	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77278966	AAGCTAGTAACACTT[C/T]CTAAGCAGTTTAGTT	23077
rs184095105	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77240864	AGAAAAGATATTCAC[C/T]ATATATTGTTTTACC	23077
rs184184549	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77084862	CAGCTCTGTACCACT[A/G]GTGCCCTGCTTCCCA	23077
rs184228181	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075673	TTTGTTGATTTCTTT[C/T]TGGGGGGGGTGAGGG	23077
rs184251174	snp	A/G	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77071766	AAAGAAGAACAGCAG[A/G]GTTCACATTTTTTTG	23077
rs184301288	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77185523	TAGAGATTAAGTGTA[A/G]TCCCAATTTTTAATC	23077
rs184301569	snp	C/T	0.00438332	0.0466095	intron-variant	MYCBP2	GRCh38.p7	13:77156441	AATACAGTATAAAAA[C/T]ACTTTTTAAAACCAG	23077
rs184319166	snp	C/G	0.00478085	0.0486577	intron-variant	MYCBP2	GRCh38.p7	13:77116404	GGAGTCTTAAATGTT[C/G]GCACTTTGCCACATT	23077
rs184326055	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77092104	AAAAAAACCTCATTT[G/T]GATATATATGTCCCA	23077
rs184360886	snp	A/G	0.000285151	0.0119371	intron-variant	MYCBP2	GRCh38.p7	13:77056958	ACAAAAGAAAAAGAA[A/G]GTACATGATTTCAGA	23077
rs184362145	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77050819	CACTCATGATGATGA[A/G]CCTGCTTCCTAATTC	23077
rs184363572	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075295	ATGATACAGTTTAAA[A/G]TGAGGAATTTCTGTA	23077
rs184370656	snp	A/G	0.00478085	0.0486577	intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326405	CACACACACACGCGG[A/G]TGCACGCGCGGCATG	23077
rs184377314	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77304151	CAAAGGAAAAAAATC[C/T]GTATGTTGAAAAGAT	23077
rs184381797	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77116018	CCTTTGTAGTCAACA[G/T]AATTGACCTCAAGTT	23077
rs184386573	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77095807	ACACAAACTATACTT[C/T]CTTTCCTTCTTCAGA	23077
rs184402257	snp	A/G	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77130166	AATTTTATTGCTTAT[A/G]TAAATATTATGATAA	23077
rs184418865	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77091379	GTTTTCAGAGGAAGT[G/T]TTCTACTAACTTAAA	23077
rs184425147	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77215545	GACAGGTAAGAAAGA[A/C]CCTTGTGGGAATGGA	23077
rs184430336	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77136237	TGTAGTGACTTCCAC[A/G]TGCACTGCACTTCAG	23077
rs184430500	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77205919	ATTCTTAAAGTGCTA[C/T]TTGAGGAAGACACAT	23077
rs184442494	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77175188	CCTCCCTCCCTGGTG[C/T]CTCAAAAGTACTGGA	23077
rs184442684	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77196485	CTGTAATAATACAAA[C/T]GAGAATGGCTGTGGC	23077
rs184451934	snp	A/C	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77097115	CACATTAATGGCACA[A/C]CCTTTGGGTAACACA	23077
rs184458604	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77155707	TTGAGTCTTTCAAAA[A/C]TATACACAAAATTTA	23077
rs184459912	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77135585	TGAGTCCTCAGTTAA[C/T]ACCTGTACTGAAGTA	23077
rs184461936	snp	A/G	0.0123036	0.0774623	intron-variant	MYCBP2	GRCh38.p7	13:77199702	GGAGATCTGAGAAAG[A/G]GCAGACTGCCTCCTC	23077
rs184471389	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087419	ATGCAAATTATTGGA[C/T]TATTTGAAGGTATAC	23077
rs184473318	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77161675	TTTGTTTTTTTCTCC[C/T]GAAGGATTTTTGTCT	23077
rs184494903	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77070922	TAGGAAATTCAGAGA[A/G]GTATATTCTCCTTTC	23077
rs184504883	snp	A/G	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77280665	ACAGTAAGACTGCCT[A/G]ATGAACAGGTTCTTG	23077
rs184525258	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77241933	AATAAGCATTTAAAA[C/T]ATGCAATATCAGTAA	23077
rs184536425	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77111402	GTAGATGTCATTTGA[A/G]ACTGGCTCCTAACTT	23077
rs184560509	snp	C/G	0.00438332	0.0466095	intron-variant	MYCBP2	GRCh38.p7	13:77140419	TTTCTAAATACTGAA[C/G]ATACGTGTTAAGAAG	23077
rs184563854	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075076	AGCTGGGCACGGTGA[C/T]GTGCACCTGTAGTTC	23077
rs184575601	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77102513	AAATTTAATTAAATA[A/T]TACTTTAAGACAAAA	23077
rs184584645	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77182704	AAACATACTACTCTG[C/T]TACATGGATGCAAAG	23077
rs184597021	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77212691	CCTAAATTATTTCAT[C/T]TATGTTTTAAAATAA	23077
rs184623008	snp	C/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77314602	TGATTACCTGGGGTT[C/G]AGTGGCAGAGAAACA	23077
rs184632196	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77294701	AGGTTGGAATGACTG[C/T]ATTTGTTAGAGGTTT	23077
rs184644578	snp	A/G	0.000399281	0.0141238	missense	MYCBP2	GRCh38.p7	13:77181816	ACTTCTCCATCATAC[A/G]CAATCGGGAAGATGG	23077
rs184656617	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291029	AAAGACTTAAATAAA[C/T]GGAGACATATACCAT	23077
rs184657957	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77299361	CAATTCTTATGAATC[C/T]GAACCCATCAATTCT	23077
rs184673895	snp	G/T	0.0103295	0.0711199	intron-variant	MYCBP2	GRCh38.p7	13:77221601	TGAAGTGCCCTCTTT[G/T]CTGCATACATGACTG	23077
rs184682139	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77264687	TAGAATAGTACACCA[C/T]ATACTTTGATCAAAA	23077
rs184685941	snp	A/C	0.00676609	0.0577691	intron-variant	MYCBP2	GRCh38.p7	13:77160841	TCTTCCATTCTAAGA[A/C]CTTTCCATCTGGGGC	23077
rs184691324	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77246855	AACACATTAACAGAA[C/T]GAAAGAAAAGAAACA	23077
rs184694356	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77251008	ATAAGAATTATAATA[C/T]TTTCTTGGCCTTTTG	23077
rs184696058	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77285161	CACCCTAGGAATCCA[C/T]TGTTCTTGTTTATGC	23077
rs184699247	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77121210	CAGCAAAAAACAATA[C/T]TATGAAAAGAACACC	23077
rs184742981	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77233963	ACATTTTGGAAACAT[C/T]TTTCATTAAATCATT	23077
rs184747109	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77080801	ACAAAAATTAGCCAA[C/G]CATGGTGGCGTGTGC	23077
rs184751378	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77052143	TTTCTTTCTTCCCCT[C/T]CTACCTTCCTTCCCT	23077
rs184766280	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77225876	TAACAGTTTATATGG[G/T]AAAATTTAGTTTCCA	23077
rs184769686	snp	A/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77246337	GACTGACACTATTTT[A/T]AAAATAGTGTTTATG	23077
rs184772749	snp	C/T	6.64772e-05	0.00576491	synonymous-codon	MYCBP2	GRCh38.p7	13:77206786	GGCATCAGCAACCAC[C/T]GCATTGTAACACCAC	23077
rs184794477	snp	C/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77186249	TTAAATTACCCTCAA[C/T]AGTAACTTTGAAGTT	23077
rs184800297	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77309067	GAACATCTCCTACAG[A/G]TTATCTAATCCAAAA	23077
rs184802557	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77168149	CTACTACTATTGCAA[A/G]TCACAGCATGAAGTT	23077
rs184805686	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77145739	AAATCTGAAGTTAAC[A/G]GAATTACTTACGGGC	23077
rs184823472	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77055048	GTGAAGGTATAGATG[C/T]AAAAGAGGTCACCCA	23077
rs184831840	snp	A/C	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77270067	GTATATATGGCCCTG[A/C]AAAAAAAACAAAAGT	23077
rs184845125	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77264090	AAGTCAAAATGAGAG[G/T]TCTCCACGCAATAAG	23077
rs184915079	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77269708	AAGAACTCTAAAGAA[A/G]GTATGTTTAATCCCA	23077
rs184921566	snp	C/G	0.000165678	0.00910009	intron-variant	MYCBP2	GRCh38.p7	13:77243010	GTGGTTTCAGGATAG[C/G]GTAGGAAAGTGGATT	23077
rs184931449	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77249860	AAACATAAAGCACTA[C/T]AGAATAAATATTATC	23077
rs184931590	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77289954	CACAGACTGGGAGAA[A/G]ATATTTGCAAACCAC	23077
rs184933305	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77175962	ACTCCATCTAAAAAA[A/T]AATAATAATAATAAT	23077
rs184937748	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77222061	ACAGATGCAATTATC[A/G]TAGGCCTAACTATGT	23077
rs184939770	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77182934	AGATTTAGGAGTTTC[C/T]TTATATCCTACTTTC	23077
rs184953410	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77162969	ATATACAGAGTAATG[A/T]ATGCAAAAATGGGAC	23077
rs184957273	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77327777	TATCTCTTGGCAGTG[A/G]TCATTTAATGGTTTA	23077
rs184959108	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77142083	CCACTATTAGATAAG[A/T]TGATGAAAAAAACTC	23077
rs184997868	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77308783	AGCCAGTTACCCTGA[A/T]GGGGAACTAGGGCCT	23077
rs184998397	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77047631	TGCAGGCACCGATGA[A/G]GGAACTAGCACAGGG	23077
rs185001636	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77259760	AAACTCAAAGGCTTT[A/C]CATATTTATCACACA	23077
rs185008461	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77069181	CATTATGTTCATAAG[A/G]TGCTTTATAGCTGAT	23077
rs185018279	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77088048	CTCCGCCTCCCAAAG[C/T]GCTAGGATTACAAGC	23077
rs185036998	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77109842	TACACCTGTTTTTAC[C/T]GCAATCTCTGAACAT	23077
rs185136489	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77151004	TAATTGTCACTGACA[A/T]CAAAATAAGCAACTT	23077
rs185153281	snp	A/C/T	0.00636936	0.0560724	intron-variant	MYCBP2	GRCh38.p7	13:77111921	AAGACCCTTCATGAT[A/C/T]CAGCCCCAACCTCTC	23077
rs185179467	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77105745	TTTGATTCTTTTTTG[G/T]GTATCACTAAGTTTA	23077
rs185192883	snp	C/T	0.00438332	0.0466095	intron-variant	MYCBP2	GRCh38.p7	13:77056458	ATTCTTCAAAAACAG[C/T]TTTTTGTTAATCATT	23077
rs185218723	snp	A/G	0.000929584	0.021539	intron-variant	MYCBP2	GRCh38.p7	13:77251142	TTAGTAGGAATCATT[A/G]TCTCTTACCCTCCGG	23077
rs185237921	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77234579	TATGACTACTACAGA[C/T]AGAAACATGCTAATT	23077
rs185244508	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77165938	CAAGAAAGTGGTTTA[C/T]GAATTCTCTTACAAT	23077
rs185245428	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77172517	ACTGATTGTAGGAGA[A/C]CAATAGTGAAAGGAG	23077
rs185246783	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77065225	GTGTTCCTAAATATT[A/G]CTCCTAAATATTTTA	23077
rs185253094	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77084594	CACTGCCCTTACTCC[C/T]AAGGCATGGTCTGTA	23077
rs185255241	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77213195	AAATGTAAACAGGGG[C/T]CAGGTGCAGTAGCTC	23077
rs185257874	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77130494	ACTAATTCATAAATA[C/T]AAGACATATAAAACT	23077
rs185262648	snp	C/T	0.0256215	0.110247	intron-variant	MYCBP2	GRCh38.p7	13:77142907	AAAATCAGAAAAAGT[C/T]CAAAATCTAGAATAC	23077
rs185262886	snp	A/G	0.00478085	0.0486577	intron-variant	MYCBP2	GRCh38.p7	13:77192976	TCTACTAAAAATACA[A/G]ACATTAGCCGGGCCT	23077
rs185266039	snp	A/G	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77173456	TTTTGTATTTCAGCA[A/G]CAACAATGAACTACA	23077
rs185266282	snp	C/T	0.0126979	0.078662	intron-variant	MYCBP2	GRCh38.p7	13:77122646	AGTGAGCCGAGATCG[C/T]GCCACTGCACCCCAG	23077
rs185277200	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77169048	ACCTCAGTTAACATA[A/G]TCTTTCCTTACATAT	23077
rs185296254	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77125677	TATTTATGAATTTGG[C/T]TAAAATAATAACTTT	23077
rs185321922	snp	A/G	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77313965	GAGATTCTACTACAC[A/G]CCTATCAGAATGGCC	23077
rs185355251	snp	A/G	0.00795532	0.062565	intron-variant	MYCBP2	GRCh38.p7	13:77237560	TTAGAAGATGACAAC[A/G]AAATAAAAACAATAA	23077
rs185359416	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77274762	TATCTCTTACCATTC[C/G]CTTTTGCCCCAATAG	23077
rs185364316	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77064895	GAACTAAAATTTCTT[C/T]GTGATCCTATGGAAA	23077
rs185365011	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77207448	CCTCTTTTAGGGGTC[G/T]GGAAGTGAGGGATGC	23077
rs185380899	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77108532	TTAGTTGCAAGGGAA[A/G]AATATTAATTATACA	23077
rs185399159	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77146460	ACAGATAACATCTTT[C/T]GAGTACATTAAAATT	23077
rs185423630	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77066974	ATACTTCTATATTAT[C/G]CTAACAAGTCATTGT	23077
rs185424120	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77109371	TGAGAATCTAATGCC[A/G]CAGCTGATCTGACAG	23077
rs185446413	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77293741	AAAACTCAACCAACC[A/G]CCACTGGCTTTGAAG	23077
rs185458934	snp	A/T	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77325811	AAGGCCCGGTTATCA[A/T]AGTACAGCTCTAAAA	23077
rs185466071	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77226239	CACTCCTTCTTTCCT[C/T]CTCCCTTCTCACAAT	23077
rs185479773	snp	C/T	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77187113	ATGTGCTAAGCCCTA[C/T]AGTTTACCTTTTAAA	23077
rs185483544	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77187644	CCATGATATATAATA[C/T]GAAATTTTCTAAAAA	23077
rs185485002	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77255114	TTTTGATACATATAC[C/G]CAGAAGTGGAATTGC	23077
rs185489075	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77125167	TGCATTAAGTACTCA[C/T]GTATTTTACAAACCA	23077
rs185492784	snp	C/T	0.00597247	0.0543191	intron-variant	MYCBP2	GRCh38.p7	13:77256482	TATCAGTAAATATTA[C/T]CAAATAAATAAGAAA	23077
rs185495876	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77169184	GAGGGCGAGGCGGGC[A/G]GATCACGAGGTCAGG	23077
rs185501904	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77217102	GTTCTTAGTTGTGCA[A/G]TCTTTCTGTAAGTTT	23077
rs185506513	snp	A/G	0.00478085	0.0486577	intron-variant	MYCBP2	GRCh38.p7	13:77284341	GAAAAGGAGCAAACT[A/G]GGATAATAGCAGCAT	23077
rs185513559	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77148033	AACTGAAGCATGTTC[A/G]TAGGAAACTAAAAGA	23077
rs185515205	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77126186	AATTATGTATTTGCA[A/G]TACAAGTAAAGATAA	23077
rs185543899	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77046378	TAGTTTTCAAAATAA[C/T]AAATCTAAATTCTGA	23077
rs185549811	snp	C/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77197037	GAAGTGTAGTGTCGT[C/G]GGGGACAAGAGAAGA	23077
rs185557615	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77132933	TTAATTTAAAATCAA[A/T]CAATGTTCCCCAGGT	23077
rs185563648	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77086928	TATTTCTTCTTACAA[C/T]TTCTTCTCATATTTT	23077
rs185571016	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77114389	AATCCCATTTTATAA[G/T]GAGGTAACAAAAATT	23077
rs185585873	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77231949	CTTAAATATTTATGG[C/T]ATTGTTAGAGCACTC	23077
rs185595653	snp	A/G	0.00874735	0.0655527	intron-variant	MYCBP2	GRCh38.p7	13:77191591	TTCCTAAGCTTTTGA[A/G]TCCTGCTGAAAGTAC	23077
rs185596666	snp	A/T	0.0256215	0.110247	intron-variant	MYCBP2	GRCh38.p7	13:77276669	GATTTTTTGGGGGTT[A/T]TTTTTTTGGTAGAGA	23077
rs185621745	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77214499	TGGAGTGATTTCTAG[A/G]AGAGATGCTGAAGCG	23077
rs185626022	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77260660	ATAATGGTTTGTATA[A/T]AAAGCTAAAAAAAAA	23077
rs185626157	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77281569	TTACCTTTACTGCTG[C/T]TCTCAAATAATTAAA	23077
rs185627028	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77303743	CACAAAATGCATCTC[C/G]TTTTGCATACACATA	23077
rs185631947	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77223492	TATTACTTTTGACCA[A/G]AAGTATTCTGACTGC	23077
rs185636531	snp	C/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77238347	ATCTACAGCTCACAA[C/T]TATGAAACTTGGATA	23077
rs185640464	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77244121	AGAAAAGATATAAAT[A/T]GCAGAATAATTAAAA	23077
rs185642173	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77193768	GTAATCTGAATTATG[A/G]TCAAACATGACCACT	23077
rs185654289	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77153111	TATTCACGCATTCAT[C/T]GCGTTTCAAACCATT	23077
rs185675083	snp	C/T	0.00874735	0.0655527	intron-variant	MYCBP2	GRCh38.p7	13:77287596	TTCATAGGTGATTTT[C/T]TTTTTTCCTAATCAA	23077
rs185679259	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77321706	AGCCAGCCTAGAATG[C/T]CATGCCTTTGTCATA	23077
rs185687565	snp	C/T	0.00914312	0.0669923	intron-variant	MYCBP2	GRCh38.p7	13:77301252	AAACCCCGTCTCTAC[C/T]AAAAATGCAAAAAAT	23077
rs185690181	snp	A/C	0.0700422	0.173537	intron-variant	MYCBP2	GRCh38.p7	13:77307639	TCAAAAAAAAAAAAA[A/C]AAAAAAAAAAAAAAA	23077
rs185706864	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77268031	ACAGGTTTTTGAGGT[A/C]CAATAATACATCAAT	23077
rs185733656	snp	A/C	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77210511	ACCACAATAAATTTC[A/C]AACAAATGCAACATA	23077
rs185750016	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77320889	GGCCCTGCCCTTAAG[C/G]AGCTAGATTTATATG	23077
rs185761939	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77281131	GAAGTCTTATAGTCA[A/G]TGAAAACACATATTT	23077
rs185764330	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77296755	AAAATGGGTATTTCC[A/G]AAGTAGACATTTGGA	23077
rs185766163	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77257209	CTCATGAAGATAGAG[A/G]GTACAATGCTGGTTA	23077
rs185774060	snp	C/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77278199	TTTCCTTTTCCCCTG[C/T]TTTTTAAAACTATTG	23077
rs185775406	snp	A/C	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77322137	TTGCACTCCAGCCTG[A/C]CTCAAAATAAGTAAA	23077
rs185777632	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77218899	TAGTAGTTTGGGTAA[C/T]TTATGATGAAGGCCT	23077
rs185781740	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77239482	AAGTGACTCAGATCT[A/G]TTTCCAAGACCCTTG	23077
rs185795179	snp	C/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77244944	CCATCAAAAAGTGGG[C/T]GAAGGATAAGAACAG	23077
rs185826079	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77316218	ATGAGCTTAACAAGA[C/T]CAGAGATACAAGGTT	23077
rs185893933	snp	A/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77302117	AGAAAGAGAGAAAAA[A/T]GAATGGAACAAAAGC	23077
rs185906064	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77046995	GTGGTGACACAAACT[G/T]CAGCCCTTGGGTTTT	23077
rs185912750	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77067967	GGGTCTTGCTTTGTT[A/G]CCCAGGTTGGAGTGC	23077
rs185934278	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77261752	ACAGAGACACAAAGT[G/T]AGCACAGGCGGTTAG	23077
rs186024555	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77054045	GGTGGTGGTGTTGAT[A/G]GAAGTGAGATGGGGG	23077
rs186025268	snp	A/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77061026	CCATAGAACACTCTA[A/T]ATATTTAGTAAATAT	23077
rs186036699	snp	A/G	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77073635	CATGATTATCTAAGA[A/G]AACCCCAAAGAGTCT	23077
rs186053136	snp	A/G	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77122440	GTCGCGGTGGCTTAC[A/G]CTTGTAATCCCAGCA	23077
rs186067952	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77131682	ATTTCACAGATTATT[A/G]TAAGCACAGCTTGTG	23077
rs186084022	snp	C/G	0.0111196	0.0737302	intron-variant	MYCBP2	GRCh38.p7	13:77092807	CTGATACTACCATAC[C/G]TAAGTTAGGAGGCAC	23077
rs186104885	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77053505	TAAACGGTCGTTCAC[C/T]AGCTAAACCTAACCC	23077
rs186125145	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77202325	CCTGGACACATACAC[C/T]CTCCCAAGACTAAAC	23077
rs186171331	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77230098	GATTCAGTCTATATA[C/T]TCTGCTTTGCCTTTA	23077
rs186175382	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77266977	TATATTTAAAAATAA[A/G]CATGCAGCCCAGGAG	23077
rs186182746	snp	A/C	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77247943	CTATTACAAAAAAAA[A/C]CAAAAAACTCTTAGA	23077
rs186186378	snp	C/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77209139	TTAATCTCTGTTTTC[C/T]AACAATGGAGAAATT	23077
rs186187608	snp	C/T	0.00755907	0.0610114	intron-variant	MYCBP2	GRCh38.p7	13:77152128	TTGTTCTTAACAACG[C/T]GATTCTATGGAATCA	23077
rs186195232	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77138002	TAAAATACACTTTCA[C/T]AGAGGGTCAAAATCC	23077
rs186201981	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77117967	ATTGTCATACATTTC[A/G]TAGATACCAAATTCA	23077
rs186203172	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77169533	CAAAGATGCAAGTTT[C/T]TGTAAAGACAAGACA	23077
rs186204935	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77188001	GCTTGAACTCAGGAC[A/G]CGGAGGTTGCAGTGA	23077
rs186209407	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77112910	ATCTTGTATCTTCTC[C/T]CTTAGTATCTTCTCT	23077
rs186210311	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77183582	TTTTGAGATGGAGTA[C/T]CATTCTGTCACCAGG	23077
rs186226715	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77142575	TAATTGGTATTATTA[C/T]TATCTCCACCCTGTT	23077
rs186239292	snp	C/G	0.00438332	0.0466095	intron-variant	MYCBP2	GRCh38.p7	13:77104731	TGACACCTTAGAACC[C/G]ACAACTGAATTTGGC	23077
rs186242280	snp	C/T	1.65299e-05	0.00287483	missense	MYCBP2	GRCh38.p7	13:77224466	CTGGAGTTGACATCT[C/T]CATGTCCTAGCTGCC	23077
rs186244331	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77073021	TCACATACCATGCTA[C/T]TCATCTGTTTAAAGC	23077
rs186245928	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77238795	CAGTAACTAAATTAC[A/G]TCAATAGGCCTGAAG	23077
rs186262372	snp	A/C	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77252755	GCAAGCAGAAAAATT[A/C]GATAACCAAGCATCA	23077
rs186263220	snp	A/T	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77217787	AGCTAATATAGACAA[A/T]TTATAAGGCAATGGT	23077
rs186265913	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77178484	TAAGATTGAATACTA[C/T]GAATATATACAGTGA	23077
rs186269886	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77197700	GAACCTACAAAGAGA[C/T]AGAAGAAAAAACTAC	23077
rs186278098	snp	A/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77158283	CCTAGGAGAGAAAAA[A/T]ATGAGACAATATTTC	23077
rs186298605	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77083747	TTAATAATATTAACT[A/C]TGGAATAACTTTTTA	23077
rs186310428	snp	A/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291616	CTACTAAAAATACAA[A/T]ATTAGCCGGGCGTGG	23077
rs186316595	snp	C/T	0.000152894	0.00874205	intron-variant	MYCBP2	GRCh38.p7	13:77262138	CCTGTACCTGAAATA[C/T]GAGACTAATAAATAC	23077
rs186332918	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77310517	TGCAACAGAGACTCT[A/G]TGGCCCATAAAGTCT	23077
rs186339492	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77245163	CTGTTGGTGGGAGTG[C/T]AAATTAGTTCAACCA	23077
rs186340914	snp	A/G	0.00111991	0.0236369	synonymous-codon	MYCBP2	GRCh38.p7	13:77058341	CAGACAGTGCTCTTC[A/G]TTTTTAACACCCCCG	23077
rs186344753	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77136681	TTCAAATATTCATTG[C/T]ATTTCTCAACCCCCT	23077
rs186346666	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77292008	AGACTGCTCTGCATG[C/T]ACGAACATCAAGCTT	23077
rs186347183	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77117200	AGAAGGAAAAAACTA[C/T]TTCGCACATGTGACA	23077
rs186350362	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076116	CAGGACCGAAAAAGT[A/T]AAGCAACTGTATTTT	23077
rs186360690	snp	A/G	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77227916	AATAATACTAGAAAC[A/G]TTTTGTTCATTGAAA	23077
rs186361607	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77164893	AGCCAACTGAGCAGG[G/T]TCAGGGCAGGTATAA	23077
rs186366760	snp	A/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77158618	CTGGCTAATTTTTTT[A/T]AAAACTTTTTGTAGA	23077
rs186375513	snp	A/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77118921	CGGCAGTATATTTCA[A/T]GCAGAAAATAAGCAA	23077
rs186395572	snp	C/G	0.00210437	0.0323691	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77077025	TTAGGGCTATGAAAA[C/G]AAAAAATGGGCAACA	23077
rs186398090	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77304545	TATATAGCACCACAG[G/T]GTGACTATCATAAAC	23077
rs186401263	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77317720	GACGTGGCCGGATCA[C/T]GAGGTCAGGAGTTCG	23077
rs186406283	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77282558	TTCAACTTTTCAAAG[A/C]TATTTTTTCAAACAA	23077
rs186416352	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77236148	ATAGGCAAAGAAAAG[A/G]AGCCTCAGCTAAGGA	23077
rs186461807	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77201858	AACGAGAACAAAGAC[A/G]CAACATACCAGAATC	23077
rs186463138	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77198057	AAAAAATATCCTCCT[A/G]ATGAGCTTATTAGAC	23077
rs186468047	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77266162	TCTATTAAATGTGCA[A/G]GGTTTCTCAGAAGTA	23077
rs186469401	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77113780	CAGCTCAGTGAAGAT[A/G]AATTCAAGCCCATGC	23077
rs186522520	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77273392	GAGTGAGAAAAAGCA[G/T]AATTCCTATTGACAG	23077
rs186540817	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77311165	TTAAAATTCCAAGTT[A/G]AAACTCTTTCTGGCC	23077
rs186542656	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77314985	TCCCATAGACCTTAA[A/C]GGATAATGAAAGAAT	23077
rs186555651	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77208528	CAGACTACAGAATTC[A/C]ACAATTTTAATAATG	23077
rs186564460	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77248106	TGTAACTAACCTGCA[C/T]GTTGCGCACATGTAC	23077
rs186566731	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77179845	ATCTTTGCTTTTCAC[A/G]GGGCATGGTGGTGGG	23077
rs186572661	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77277271	TAAAATAAATCAAAT[A/C]TTCAGTAAAATGCTG	23077
rs186573902	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77138775	ATTAGACAGAACACA[C/T]AGAACTATCTGCAAA	23077
rs186596652	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77099436	TCCAGCAGAGTGATA[C/T]CTCGCATCCTTAGGG	23077
rs186599730	snp	A/G	0.0144041	0.0836335	intron-variant	MYCBP2	GRCh38.p7	13:77273710	ATTCATCCAACATAC[A/G]GAACATTATATGCGT	23077
rs186614889	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77253723	TGCATGCATATTATA[A/C]TTCAATGTAACAAAT	23077
rs186620786	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-5-prime, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77292424	ACACACACATACACA[C/T]ACAAGTGCATATATA	23077
rs186627122	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77185552	TCTAAATGGAAGGGG[G/T]AATAAAAACCTAGTT	23077
rs186631116	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77236272	GAGAGGAGTGAGTAA[A/C]ATAGGGGTATGAGAT	23077
rs186635845	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77167363	TCCTACCAGAAAGCA[A/C]GGAAGCTAGGAATGA	23077
rs186637042	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77195396	GAGGTCACGAGTTTG[A/T]CACCAGCCTGGTCAA	23077
rs186640129	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77214884	AACACCTTAGCATAC[A/G]CAGTCCATCACTGAC	23077
rs186654293	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77286350	TTTTGAATAGCTCTG[C/T]TTAGAAAAAAGCAAT	23077
rs186655803	snp	A/G	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77247254	GAAAATGAATTCAGC[A/G]AAGTAGGAAGATACA	23077
rs186676093	snp	A/T	0.00103142	0.0226859	intron-variant, nc-transcript-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77083016	TGTACCTAGGATATG[A/T]GGATACCAAAATTAC	23077
rs186814229	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77256746	AAATGTTGGAGAGGA[C/T]GTGGAGAAAAGGGAA	23077
rs186820283	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77230152	GAATTCTGACCTTCT[C/G]TGAATTTTCTCCAAT	23077
rs186822313	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77308587	TGCTAAACACATTTT[C/T]ATTATTATTCCCATG	23077
rs186824160	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77295877	GAGCTACCAACAGTC[A/C]AAAGAGGCTCAGAAC	23077
rs186880604	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77063915	TAAATTGACTTTTTC[C/T]GCCCTAGGGATATAT	23077
rs186912077	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77086265	ACCAACTGACAGCCT[C/T]TTAAACAAACTCAGT	23077
rs186934441	snp	C/T	0.00597247	0.0543191	intron-variant	MYCBP2	GRCh38.p7	13:77103794	ATCTCAGAATGGACT[C/T]GGGGTGACACTGTGT	23077
rs186935552	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77209836	CTGAATGCAAGCCTC[A/G]TTATTAATCTCTATT	23077
rs186942015	snp	C/T	3.29576e-05	0.00405928	intron-variant	MYCBP2	GRCh38.p7	13:77059519	TGTGTCACTATATAC[C/T]CACCTGGCAATCTGC	23077
rs186942286	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77145223	CACCAATGACCACCA[C/T]GTCCCCAAGTTCAAT	23077
rs186944372	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77124934	TCAATGCTCTTTCCC[C/T]AAGACAAAATGCAAT	23077
rs186953264	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77169833	TATAGTTGACACCAA[C/T]TGGGTGCTTGTCAAG	23077
rs186953382	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77107803	TGATTTGTATATACT[C/T]TTAGCTATGGCAGCC	23077
rs186963059	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77255212	TCCATAGTTGCTGTA[A/C]TAATTTACATTTCCA	23077
rs186969374	snp	A/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77283545	AATCTTTTAATAATG[A/T]GGCATGACTGGCTTC	23077
rs186977981	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77237692	TTAAAGGGAATACAA[A/G]CAGGACACCAATATC	23077
rs186978174	snp	C/G	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77324085	TTGAAATCCCCTTGA[C/G]TTACCAAAAACACAT	23077
rs186987276	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77303075	CGCGGTGGCTCATGC[C/T]TGTAATCCCAGCACT	23077
rs186988179	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77069505	AGCAGTTTGGGAGGC[C/T]GAGGCAGGTGGATCA	23077
rs187003616	snp	C/T	0.00119737	0.0244387	downstream-variant-500B	MYCBP2	GRCh38.p7	13:77044319	GAGCTGAGATCACGC[C/T]GCTGTACTCCAGCCT	23077
rs187005718	snp	C/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77263430	AGAGAAATTATTAGT[C/T]AATTCCTTAGAATGG	23077
rs187007527	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77215568	GGAATGGATTGGAAG[C/T]AGAAGTCACAGTGGG	23077
rs187014627	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77066349	TACAGTCCAGGGACC[A/T]CACACGACTTATTTC	23077
rs187023132	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77085374	ACAGTCAATTTCCAT[A/C]GACATTTGTGTGTAT	23077
rs187043750	snp	A/C	0.00557542	0.0525036	intron-variant	MYCBP2	GRCh38.p7	13:77148946	AATGAAACAAGCACT[A/C]CTCCTCCTCCTATTT	23077
rs187052187	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77093722	CAGAGCCATTCTCTC[C/T]TCTCATTCCCTATCA	23077
rs187058640	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77177223	CTTTAATTCTACTTT[A/C]AATCTTTCTCTTTCT	23077
rs187062126	snp	C/T	0.00597247	0.0543191	intron-variant	MYCBP2	GRCh38.p7	13:77110069	TGAACAGAACAACAG[C/T]GATTTTCAAGGAACA	23077
rs187103312	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77298857	TATACCTGCTTATAG[A/G]ATCTACTCAACTACT	23077
rs187107822	snp	C/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77280148	CTGAAGGTAAGTCAA[C/T]TGTAGTTCTGATTAA	23077
rs187111897	snp	A/G	0.00914312	0.0669923	intron-variant	MYCBP2	GRCh38.p7	13:77320575	AAGCATTAGGTAAAA[A/G]GCATTCACAATGTGC	23077
rs187127260	snp	G/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77188458	CCTTAATTTATACTT[G/T]CATTTATTTACATCA	23077
rs187143310	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77258838	TCTTCATAACAACTA[C/T]ATGAAGCAGGTGCTA	23077
rs187147533	snp	C/T	8.25008e-05	0.00642212	synonymous-codon, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076784	TCCTTCAGGTGATGA[C/T]AATAGTGCTTTTTCC	23077
rs187153352	snp	C/T	0.00716266	0.059414	intron-variant	MYCBP2	GRCh38.p7	13:77297314	TTAATATGTTTTATG[C/T]TCACCATGCTGAGAT	23077
rs187154642	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77241454	ACCTAATATTTCTAA[A/C]GAAAGAAGAAACAGG	23077
rs187171949	snp	C/G	0.00119737	0.0244387	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77328623	TGGAGTGAGAACCAA[C/G]ACAATGGTGTAGAGG	23077
rs187182952	snp	C/T	0.00874735	0.0655527	intron-variant	MYCBP2	GRCh38.p7	13:77129550	CTTTAAATGAGGATG[C/T]ATTTGTTCTAATACA	23077
rs187186348	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77111131	AATCCTTCCTAAATT[A/G]AGTGCAAAATCATGA	23077
rs187194491	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77090818	TGTTGTATTTACACT[C/T]TATAAAAGAACTTAA	23077
rs187203577	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77258122	TAATACCTCTCCACA[A/G]TACTTTCAAACTTTT	23077
rs187204031	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77088186	AAAATAATTTATAAG[A/G]TACAATACCAAAATA	23077
rs187209264	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77152523	TCCGCCTAAATGTTG[C/T]CTTTTTGGCCAGCCC	23077
rs187217360	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77241079	AGTCAGATACAACAA[C/T]ATAATTTCTTTAAAT	23077
rs187225876	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77198822	GTCCCTAAACAGTTG[G/T]GCCTCCTCTGTCATT	23077
rs187227702	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77220448	CCCAACCTAGAGACT[G/T]AACTCAGTCATTCTG	23077
rs187233774	snp	A/G	0.0185938	0.0946107	intron-variant	MYCBP2	GRCh38.p7	13:77210232	TTGAGACAGAGTCTC[A/G]CCCAGGCTGGAGTGC	23077
rs187238618	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77181590	GCACCAAGCTAAATA[C/T]GCTTAGCTTGGTGTG	23077
rs187247438	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77127279	TTTAAGTAAATATAA[C/T]GTAAATTTATTATTG	23077
rs187250102	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77190368	TGATACCAAAAACAA[C/T]ATGATCATTACAGGA	23077
rs187250455	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77157425	CACAGGATTTCACCA[C/T]GTTGGCCAGACTTGT	23077
rs187251654	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77272176	CTCTATGCTATAGCT[A/G]TACTAAACTTCTTTC	23077
rs187254513	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77170654	CGATCTCGGCTCACT[A/G]CAGCCTCCGCCTCCT	23077
rs187269822	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77048437	AGAATTAACAGGGTT[C/G]AGAGTGGTTAGAGAA	23077
rs187312329	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77235360	GGAAAGGAAGAGAGG[A/G]CATTCCAGTTAAAAG	23077
rs187332694	snp	C/G	0.00874735	0.0655527	intron-variant	MYCBP2	GRCh38.p7	13:77302513	TTAGATCCATGAAAG[C/G]TGATATAATTCACAT	23077
rs187367236	snp	A/C	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77306783	GAATGAGAGCAAGCA[A/C]ATAACTAAGAACACA	23077
rs187394442	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77308913	CTGGTGGAAAGTTTT[C/T]CTGAAGGCATTAACT	23077
rs187408563	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77174088	CATTTCAATGATATT[A/G]AAGAAATAACAGCAA	23077
rs187421479	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77289970	ATATTTGCAAACCAC[A/G]TATCCAACAAAGGAT	23077
rs187428457	snp	C/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77132204	ATTGAGATTAAAACA[C/T]GGGTTATGTATACAC	23077
rs187433512	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77246220	AGTTTAAAAGACATA[C/G]CTAGACACCCTGTGA	23077
rs187445131	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77206426	TTTTAAGGGTCTACC[C/T]CTGTGAAAATTAAAT	23077
rs187484732	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77324780	GAAATCATATTACAC[C/T]AGTAGTAGGAAGTCA	23077
rs187496407	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77160291	TCCCAGTGCAGTTGC[C/T]CACTAGCTGTATGAT	23077
rs187501016	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77284308	CCACACACTTAGGAG[A/G]AGCAACAGAGGAACA	23077
rs187504928	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77252486	TTGAAGGAACACAGT[A/G]TTATAAGACCCTATG	23077
rs187514740	snp	A/C	0.00438332	0.0466095	intron-variant	MYCBP2	GRCh38.p7	13:77140261	GTTTGAAAGTATCGT[A/C]ATTCTTAATAAGGTT	23077
rs187556810	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77061555	AACTCAACCAAGGTC[C/T]TTGATTCCAAAGTCC	23077
rs187562716	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77078728	ATTCCCTATAATACT[C/T]TGGTTGTGTGCCAAG	23077
rs187566867	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77213834	TATATGTGACTCAAA[C/T]CTTCAGCAGTGGAAG	23077
rs187586268	snp	A/G	0.00557542	0.0525036	intron-variant	MYCBP2	GRCh38.p7	13:77119601	ATTAAGAGTTAAAAT[A/G]GGAACTACTGTTACA	23077
rs187602227	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77100372	TTACTCTTCACTGAT[A/G]TAATACCAAGAATGA	23077
rs187605090	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77089777	AACTGTGAATGTGTA[C/T]GTCATTGGAACTCCT	23077
rs187628429	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77322300	GTTAAGTTTAGATTC[C/T]CCATTTTGGTCACAA	23077
rs187672220	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77069976	ATATGAACAATATAG[C/T]GCTATTTCCTCACCT	23077
rs187700056	snp	C/T	9.91539e-05	0.00704039	intron-variant	MYCBP2	GRCh38.p7	13:77225404	GCACAATTGTAAAAA[C/T]GCAGTTATACCCTAA	23077
rs187701233	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77159580	CTGGCGGGAGGTGAC[C/T]GAATCATGGGGGCAG	23077
rs187704284	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77139425	GCAAAGCAGAAAAAT[C/G]ATGGTGCATGTGCAG	23077
rs187741304	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77174816	TTCAAAGTCACGCAG[C/T]TAGTAAGTGATGGAA	23077
rs187752862	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77134279	CCCAGTCTGTAATCC[C/T]AGCACTGTGGGAAGC	23077
rs187757484	snp	A/C	0.000133251	0.00816136	intron-variant	MYCBP2	GRCh38.p7	13:77263908	CATTTACACTAGCTA[A/C]TTAAGATTCAGGATA	23077
rs187761438	snp	G/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77303264	CTTGAACCCGAGAGG[G/T]GGCGGTTGCAGTGTG	23077
rs187761822	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77115694	ATTCGGAAAAAAAAA[A/C]CCAAAGAATTACAGA	23077
rs187762017	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77166223	ATAGTAGGTCTTTAA[A/T]AAATTTCTCTAAAAA	23077
rs187763109	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77144050	AAAATGCATTCATTC[A/C]TCCATATTTGCTGTC	23077
rs187767183	snp	A/G	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77095077	TAACAGAGTGAAGTC[A/G]GCCTACCAAAGAGTA	23077
rs187771823	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77055008	TCTCAAAAATTTTGG[A/G]GGGTCATAAACATAT	23077
rs187776281	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77094660	CTTTACTCACCTGGG[C/T]TATTCTTCCAAGAGT	23077
rs187803205	snp	C/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77074250	GTCTTCTCAATGAAT[C/T]GTAGTAGAACAATTG	23077
rs187803860	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77191416	TAATTTCTAATTTGG[A/T]AATCAAGCTCGTAAA	23077
rs187826260	snp	C/T	0.00438332	0.0466095	intron-variant	MYCBP2	GRCh38.p7	13:77056188	GGGGAAGGCAGAACG[C/T]CAGGTGACAGAAGTG	23077
rs187830534	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77203577	AACCAAAAAAGAGCC[C/T]GCAAGACCAAGTCAA	23077
rs187832628	snp	A/G			intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075133	GGATCCATTGAGCCC[A/G]GGAGGTTGAGGTTGC	23077
rs187838815	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77224977	AGGAATTTAACATTT[G/T]TGTTTTTATAAAGGT	23077
rs187848433	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77269667	TAAAGGTGGTCTTCA[A/T]TTCTTATCTAGAGGC	23077
rs187852831	snp	C/G	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77135279	TTTTACAATTAACAG[C/G]CATGATTAAAGTTCA	23077
rs187852972	snp	A/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77184457	AAAATCATGTGTACT[A/T]GAAAAGAATATGTAT	23077
rs187858719	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77249290	GTACTTTATCATAAT[A/G]AGATATGTAGTCACA	23077
rs187866658	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77289736	GGAAAAAGGCAAGAA[A/G]TATTTTCTAAAAAAG	23077
rs187874906	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77231727	TGAAATGTGAATATT[C/T]AACCTCAGTTAAACT	23077
rs187894403	snp	A/G	0.0174175	0.0916809	intron-variant	MYCBP2	GRCh38.p7	13:77210383	ATTTTTAGTAGAGAC[A/G]GGGTTTCACTGTGTT	23077
rs187899690	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77184575	AGTTCCTCTATTAAT[C/T]ACTGAAAGAGGAGTG	23077
rs187928572	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77106792	GACATGTGTAGGTTT[A/G]TTACATGGGTAAACT	23077
rs187972483	snp	C/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77225190	CTTCCAGACTGTCTT[C/G]AATTATAAAAGAAGT	23077
rs187992937	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77313495	ACTCAAAATGGAAAA[C/T]GGACTTTATATGTAA	23077
rs188003416	snp	G/T	0.00438332	0.0466095	intron-variant	MYCBP2	GRCh38.p7	13:77294511	AAGGGCACAAAGCTA[G/T]TTGGAGGCCGAATTG	23077
rs188015295	snp	A/C	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77276120	GCACATTCTTAGCAC[A/C]TAACAAAGGGGGTGC	23077
rs188025156	snp	A/C	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77314439	GATTATTCAGTGGTA[A/C]GAAATGAGCTATCAA	23077
rs188030096	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77154163	TAATTTTGTTTCCAG[C/T]TAATATAATATGATA	23077
rs188032583	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77199099	GAGCAACACAGAAGA[A/C]GGGTGATTTCTGCAT	23077
rs188033300	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77208725	AGGCTAGTGGAATTC[A/G]GTATGGGAAAAGAAA	23077
rs188033342	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77255903	TAGTTCTAATAATAT[A/G]TATGTATGGTTTAAT	23077
rs188036902	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77050279	GGCAGTGTGTGTTTT[C/T]TAGCTTTGACAACAC	23077
rs188040302	snp	C/G			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228581	TAAGACCAAAGCTTA[C/G]ATCTATATAAAAAAT	23077
rs188046356	snp	C/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77114767	TTAAAAATAAAACAT[C/T]ATAAAATAAAAAAAG	23077
rs188048647	snp	A/C/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77238136	CAGTCCCAGCTACTC[A/C/G]GGAGGCTGAGGCAGA	23077
rs188049023	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77160999	GGGTCTGAGTAACAC[C/T]GATCCAGTTGAGAGA	23077
rs188051828	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77230646	ATATTTTAAATAATT[G/T]GGTGCATGAAAATTT	23077
rs188053313	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77187664	TTTTCTAAAAAAGAT[A/G]AAAACTGTAAGTATC	23077
rs188064007	snp	A/G			intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77074899	TGAGAGAAATTTGGG[A/G]AGTGATGTGTTTTAA	23077
rs188076126	snp	A/G	0.0019996	0.0315563	intron-variant	MYCBP2	GRCh38.p7	13:77054403	GATTTTAGATCTAGA[A/G]GTATTAATTAGCAGC	23077
rs188112341	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77268511	CAGGCTGGGGGCGGT[C/G]GCTCACGCCTGTAAT	23077
rs188116588	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77307733	CAATACCACAAACTT[C/T]CTAGTAGCCAATTCA	23077
rs188158022	snp	C/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291337	AATGGGAAACCCCTA[C/T]TTAGTAGGCTGACTA	23077
rs188176075	snp	C/T	3.31972e-05	0.004074	intron-variant	MYCBP2	GRCh38.p7	13:77205421	TATGTTTTAAAAGAT[C/T]CATATATATTTCAGT	23077
rs188180806	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77310004	GTAGTCCCTGCTATG[C/T]AGAAGGCTGAGGCAG	23077
rs188182919	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77251418	ATAAAAGATGGATGA[C/T]TATATTTCCCAGTTT	23077
rs188187831	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77279463	CTAAAGATTGAGAGA[A/G]CAAATTGCAATGAAT	23077
rs188187944	snp	A/C	0.00914312	0.0669923	intron-variant	MYCBP2	GRCh38.p7	13:77166676	ACAGGATAAAGTACA[A/C]AATTAAAATAGAATA	23077
rs188192941	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77271328	TTGAAGTCAAGAGTT[C/T]AACCCTCCAGAAAGG	23077
rs188196777	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77234618	ACAGAAGAATAAGTT[C/T]TCAATAATGCAGTAC	23077
rs188203845	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77124416	CTTTTGAATAAAGAT[A/G]CATGTTCTCTTATTT	23077
rs188229147	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77274943	ATCCTTTCCTCTACC[C/T]TTTCCTCCAGCTATC	23077
rs188239260	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77245543	TTCTCACTCATAAGT[A/G]GGAGTTGAACAATGA	23077
rs188264377	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77303770	CATAAATGCATATAC[A/T]GAAAAAAAAAACACT	23077
rs188277126	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77318531	GAGAACGAGGCAGGC[A/G]GATCACGAGGTGAGG	23077
rs188321547	snp	C/G	0.0193772	0.0965046	intron-variant	MYCBP2	GRCh38.p7	13:77248688	AAATGGTTGGCCGCT[C/G]TGAAAAATAGTATGG	23077
rs188326861	snp	C/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77070262	GGACCTATAAAAGGG[C/T]GAGCATAAAAAAGCC	23077
rs188332839	snp	A/T	0.00126203	0.0250883	intron-variant	MYCBP2	GRCh38.p7	13:77181966	ACCAAAAAATATAGC[A/T]TCAGTATAATCTAAG	23077
rs188395173	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77066746	AATGCCTATTTCCTC[A/G]TAATGTTGCCAAAGC	23077
rs188406712	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77221182	CCTGATATTTTGTTT[C/G]AACATTAAATGCTAT	23077
rs188409648	snp	A/C	0.000438094	0.0147937	intron-variant	MYCBP2	GRCh38.p7	13:77057142	TATAATAATGATAAA[A/C]AGTTGAGTGACTGGG	23077
rs188410389	snp	C/T			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77294117	GGCTATATATATATA[C/T]ATATATATATATACA	23077
rs188410954	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77288744	CACTGTAGAGTCTCA[A/G]TGACCTACTACAAAC	23077
rs188456549	snp	G/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77109706	ATGAGTTAGCAGACT[G/T]GTTGCGGAAAGTCAG	23077
rs188466524	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77135823	CCAATGGTAAACACA[A/T]TGTTTTTATCTTTTT	23077
rs188469525	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77116021	TTGTAGTCAACAGAA[C/T]TGACCTCAAGTTCTG	23077
rs188477097	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77062197	AGATACCCATCAAAC[C/T]TACTTAAGTATATAT	23077
rs188508645	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77047051	TCAACAAATATTTAC[C/T]GCATGCCTAATATAT	23077
rs188520733	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77069052	AAATATTTAAATCAA[C/T]TACTATGTGCAAACT	23077
rs188528989	snp	C/T	0.000217502	0.0104261	missense, nc-transcript-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087611	GTGGTTTGGATGACA[C/T]TACACAGAAGCCAGT	23077
rs188539457	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77196488	TAATAATACAAATGA[A/G]AATGGCTGTGGCATG	23077
rs188542651	snp	C/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77298069	CAAAAGCACCGACAT[C/T]GTTTAAAAGATCCTC	23077
rs188543060	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77175324	AAAAAATGGTGAGTC[C/T]ATTATATTTTTAAGA	23077
rs188556447	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77101972	TCCTAATTTATTTAA[C/T]GACTGTACTTTTACA	23077
rs188560720	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77269724	GTATGTTTAATCCCA[C/T]ATTAAAGCTAAATAA	23077
rs188561683	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77128600	TAATAAGTATAAAAC[A/G]AAGTTTATCCAATTC	23077
rs188605823	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77151891	CTAGGCAACCACAAA[C/T]GTACACACAATTTGA	23077
rs188611676	snp	C/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77131543	ACACACACACACACT[C/T]GAATAGTGTTCTTTG	23077
rs188621957	snp	A/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77112605	TGATCTTTAAAAAAA[A/T]TTTTCTTAATTTTTA	23077
rs188658614	snp	C/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77234253	AATGTCTTCAAATTT[C/G]AAAACACTCTAAATT	23077
rs188669255	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77212907	CTTCCACCCCTGGCT[C/T]GGGACCTCTCTCCCC	23077
rs188677368	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77219190	CTCACAGACATCTAG[A/G]ATAAACCACACAGAA	23077
rs188687797	snp	A/C	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77173320	CAGCTTTCTGAAACA[A/C]GTAACTCTTACGCAT	23077
rs188691250	snp	C/T	1.64749e-05	0.00287005	synonymous-codon	MYCBP2	GRCh38.p7	13:77150782	CTTCACTATCATTGG[C/T]TCATATGAAACATCT	23077
rs188691995	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77192389	AGGTGTTTGGAGTCT[C/G]TCACATAATATCTAT	23077
rs188693798	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77180693	GCTGAGATGGGAGGA[C/T]CACTTGAGGCCAGGA	23077
rs188705370	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77314087	AGCCACTTTGTAAGA[C/T]AGTTTGGTGATTTCC	23077
rs188709987	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77111552	CTCCCAAGTAGCCAG[A/G]AATATAGGTGCAGCC	23077
rs188759987	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77063300	CAGTGGCACATGCCT[C/G]TAATCCCAGCACTTT	23077
rs188766145	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081370	CAGAAATGAAAGTGC[A/G]TGAATACTAAGATCT	23077
rs188770915	snp	G/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77257374	GTATACTTTAACAAC[G/T]GAGGGAGTATAACTG	23077
rs188771065	snp	G/T			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77079486	CGCAAAGCACATCAA[G/T]AAATAGATTAACATT	23077
rs188792689	snp	A/G	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77130726	GTACTTGGTCAATGG[A/G]TTTTTCTCCCTTACA	23077
rs188796270	snp	A/C/T			intron-variant	MYCBP2	GRCh38.p7	13:77123515	AGACCTAACTTACCA[A/C/T]CCATTAGCTTTATCT	23077
rs188827471	snp	A/G	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77121083	ATTTTACTAGATTTA[A/G]TGAAATAGAATCTTT	23077
rs188830330	snp	A/C/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77321795	TCTTGCACTTCCAGA[A/C/T]AGACAGTAAACTCAA	23077
rs188835863	snp	A/T	0.00676609	0.0577691	intron-variant	MYCBP2	GRCh38.p7	13:77236876	TGCCTCTACAAAAAA[A/T]AAATAAATAAATAAA	23077
rs188837650	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77149912	TAAAACCAAGTCATG[C/T]TTCTTGATCATCTGC	23077
rs188838348	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77084881	CCCTGCTTCCCACAT[C/T]CCAAAGTTACAGTCC	23077
rs188849576	snp	C/T	0.00438332	0.0466095	intron-variant	MYCBP2	GRCh38.p7	13:77196054	GTCTATGGTTGGGAA[C/T]TGAATTTACAGTTTT	23077
rs188858161	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77154737	CTTCAACATCTTAAC[A/G]TGTATTGTACTGTGA	23077
rs188869085	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77281850	TAATTCTTTACCCTT[A/G]AAAATTGTATCTTGT	23077
rs188869559	snp	A/G	0.000399281	0.0141238	missense	MYCBP2	GRCh38.p7	13:77261248	ACTAAAAGGGCGTGA[A/G]AGCCATCGTGTCCAA	23077
rs188887051	snp	G/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77183165	ATATTTTTAAGAGCA[G/T]CTATGTTTCTGAGTG	23077
rs188891093	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77163446	AGGGAGGAAAAAAAT[A/G]ACAGTGGGAAGAGTA	23077
rs188895958	snp	C/T	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77051226	CAATCACACTTAAGA[C/T]AGGCATATACATAGA	23077
rs188921445	snp	G/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77274550	CAATTCTCTAAAAAC[G/T]AAAATGCCACCTGTG	23077
rs188940308	snp	A/G	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77260197	AGTCACAGCTACAGC[A/G]AAGCTTCCCTTGCCA	23077
rs188946710	snp	A/G	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77281234	ATTTGTGTGTAAAAA[A/G]CATTTTAATGTGTAC	23077
rs188954710	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77243337	TCTCATTCTGGCTAG[A/G]CATGGTGGCCCACAC	23077
rs188962631	snp	A/G	0.0232847	0.105357	intron-variant	MYCBP2	GRCh38.p7	13:77201415	TGAGTGACCTACAAA[A/G]AGACTTAGACTCCCA	23077
rs188963894	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77172128	CTGGTCTCAAACTCC[C/T]GACCTCGTGATCCAC	23077
rs188971383	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77222161	CCCAGATTCAGCCTC[C/T]GCATTTCAGTAATGT	23077
rs188977845	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77198261	TACTCCATATAACTA[A/T]AGGAGCTTTAAATTT	23077
rs188979880	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77130184	AATATTATGATAAAC[G/T]GTTATTTTGAACCAA	23077
rs188983241	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77216433	GAAGCAGGCATCTTA[A/G]AAGTGTCAACCTACA	23077
rs188987432	snp	A/C	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77176177	ATTCTTCCCAATCTA[A/C]AGATAAGTCTCAAAG	23077
rs189006190	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77136390	ACTATATTGTTCTAG[A/G]ATTTTATTAAATCTT	23077
rs189042420	snp	A/G	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77247315	TAGACACTAACAATG[A/G]ACAATATGAAAAGGA	23077
rs189045857	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77240665	AGGCATCACTTTGCA[C/T]AGTGCTGTGTTAACT	23077
rs189049470	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77278518	CTTCATAAGAGAAGC[C/T]CTTCACTTTTTAAAA	23077
rs189052101	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77052093	CTGACTGTATGTAGG[A/G]TGGATCAGGGTAAGA	23077
rs189062384	snp	A/C	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77071830	ATTATAGGCCAGAAT[A/C]CAAATCTTAACAATT	23077
rs189079832	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77304414	TTTTACTCATATGTG[A/G]AAGCTAAAAAAGTTG	23077
rs189082384	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77106647	GTTCTCAATCTTGAG[A/G]AGGTAGTGGAGCCGT	23077
rs189089325	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77112017	TGTTCTTGGACAGGG[A/C]TAAAAGTTGATTCCC	23077
rs189091336	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77327192	CACTCCCTCCGCCTC[C/G]GGGCTTTGGGTTTGG	23077
rs189097437	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77092123	ATATATGTCCCATTG[C/T]GCTCATTAAAGTATT	23077
rs189108390	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77065660	AATGAGAAACTTCCA[C/T]TTTCGAGAGCTCTCT	23077
rs189108942	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77286529	GAGGCCGAGGCAGGC[A/G]GATCACGAGGTCAGG	23077
rs189110610	snp	A/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77215140	ATTTTTGTATAACTT[A/T]ATTTTTAGCAACATG	23077
rs189112795	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77285649	AAATTAGCCAGGCGC[A/G]GTGGCACATGCCTGT	23077
rs189121048	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77328063	AAGAGTTTCCTAATT[C/T]ACAGTCCTGACAAAA	23077
rs189134700	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77175113	TTTTAGGGTGTTTCT[A/G]TAGAGATAAGGTCTG	23077
rs189165954	snp	C/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77293374	TTATCAGTTAACTCT[C/T]GTGTAACTCTCTTTG	23077
rs189201011	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77254666	TATATTGTTGTTAAC[A/G]ACATTCACCCTACTC	23077
rs189217091	snp	A/G	0.00835141	0.0640778	intron-variant	MYCBP2	GRCh38.p7	13:77299461	TGTTGTTGTTGATTT[A/G]GTTTGCAGAGGAAGA	23077
rs189260669	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77196710	GATGGGGAAGAACAT[A/G]AGGATAGCAGGTTTA	23077
rs189281172	snp	A/G	0.00874735	0.0655527	intron-variant	MYCBP2	GRCh38.p7	13:77213419	GCCGGAGGTTTCAGT[A/G]AGCTGAGATCATCAT	23077
rs189289764	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77156836	AATTCTACCATGCAT[C/T]ACATAAAAACGTCTG	23077
rs189304074	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77116547	TCTGGAATTTGGAAG[C/T]CAAAATTTAGAGACG	23077
rs189326159	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77097141	ACACATAATATTTTT[A/T]AAAACATGCTACATG	23077
rs189328686	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77266828	TTTATTAAGTCATCC[A/G]CTTTCCAAAGCTCCT	23077
rs189374632	snp	A/G	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77141946	TAGGAAGAAGAGCAG[A/G]GAAGTTGAGTATGGA	23077
rs189378605	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77121884	AAATAAAAGTATTTT[C/G]CATATTAGTATTAGA	23077
rs189387322	snp	A/G	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77305924	AACCTACTTTTAACA[A/G]TGTATTCAACTATAC	23077
rs189389084	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77103444	AATAGTTTATATTCT[A/G]CTATATTTTTGAACA	23077
rs189427001	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77063754	CAAGAGATGTTAAAA[C/T]AGGGACAGAAAAATA	23077
rs189437037	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77082771	TGAGGTAGGAGACTG[G/T]GGAAAGTGAGGGAGA	23077
rs189446265	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77182733	AGTTGCCTGGGATGC[A/G]TTAGTGATGACAATG	23077
rs189466046	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77320638	ACAAATGGAAAAAGC[A/T]TACATTTACAGAGAT	23077
rs189466575	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77161823	TGAATGAACCCAATG[G/T]TCAAGACAAATAGGC	23077
rs189484484	snp	C/T	0.00517822	0.0506191	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076132	AAGCAACTGTATTTT[C/T]GCAAGAAATTTCAAG	23077
rs189485032	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77280702	CTGGTAAGTTTAAGG[C/T]GTAATAACAAGTGAA	23077
rs189516504	snp	G/T	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77136865	CTCTCTAAGGTGCCC[G/T]TAATTCCATTTCCTC	23077
rs189522156	snp	A/C/T	3.29457e-05	0.00405854	synonymous-codon	MYCBP2	GRCh38.p7	13:77168572	AGGGTTGAAGGCAGG[A/C/T]GGTGCATACTTCTGA	23077
rs189524591	snp	C/T	0.00953873	0.0683987	intron-variant	MYCBP2	GRCh38.p7	13:77186817	ATTTTTTTTTTTTTT[C/T]TTTTTTGAGATAGAG	23077
rs189525482	snp	A/G	0.0166325	0.0896639	intron-variant	MYCBP2	GRCh38.p7	13:77169313	AGGCAGGAGAATGGC[A/G]TGAACCCGGAAGGCG	23077
rs189529073	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77148145	TTAATAGTAGAAATA[A/T]TTTTAAAATTTGATA	23077
rs189529413	snp	C/T	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075385	TCATGGGCACACACA[C/T]GACAGTATAACCTTT	23077
rs189529735	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77226263	TCACAATTTCCTTCA[C/T]TGAGCTTGCTTTAAG	23077
rs189529954	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77117373	GGAAACCCAGAAAAG[A/T]TTATACTCTTGTGTA	23077
rs189537182	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77187224	GTTACCAAGCACAGA[A/C]AAGTGAGATCACTAA	23077
rs189538079	snp	A/T	1.66344e-05	0.0028839	synonymous-codon	MYCBP2	GRCh38.p7	13:77097458	TTTCTCTGGTCCTCC[A/T]ACTGCCAGCTGGGCC	23077
rs189541782	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77126940	TGTATATTGTTATGG[A/G]TAAAAAAAAGTCTAA	23077
rs189549007	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77109973	TAAGCTGAGAATGTA[C/G]GTCACCTCAGGACCA	23077
rs189559875	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77046014	GATTCCTGTAATTTT[C/T]AAAAGTACCTGAAGG	23077
rs189560557	snp	G/T	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77147026	AGATCCCCAATGGAA[G/T]GCTTTAAAGCAGTTA	23077
rs189568507	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77264215	TTTATAAATCTTCCA[A/T]AACCAAGGACCTGAG	23077
rs189579031	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77303818	ACTTACAACTCAAGA[A/G]GCTAGAAAGAAAACC	23077
rs189580153	snp	A/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77088058	CAAAGTGCTAGGATT[A/T]CAAGCATGGGCTACT	23077
rs189586676	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77284647	TGCTTGCATAATTTT[A/T]TTAATAAACTGAAGA	23077
rs189588959	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77226019	CTAAATAGATCTTAG[A/G]AAGGCTACACTGCCC	23077
rs189589194	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77061041	TATATTTAGTAAATA[C/T]ATAGATCAATGATGT	23077
rs189593779	snp	A/C			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075836	TCATTCAAATGAAAT[A/C]TCCAAAAGATGTTGA	23077
rs189597139	snp	C/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77246415	AATTCATTCTTTGAG[C/G]TCAGGATTACCCCAA	23077
rs189597346	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77078432	TATAGCTGCAGTGTT[A/G]TAAGTGTTATAACAG	23077
rs189603452	snp	A/T	0.00059998	0.0173098	intron-variant	MYCBP2	GRCh38.p7	13:77206873	ATGTGGTTTTGTTTT[A/T]AAAAAAAATTCCTAA	23077
rs189611786	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77157871	ATATTCTAATGACTC[A/C]CCTCTTTCAGAAATG	23077
rs189667115	snp	C/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77092581	AGGTGTGTGTCACCA[C/T]GCTCGGCTAATTTTT	23077
rs189675363	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77121258	TTAGCTTTCCATGAA[C/T]AAATTTTAATTTAAT	23077
rs189681180	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77052259	GCTGGAGCATAGTGG[C/T]GCAATCATGGCTCCC	23077
rs189710025	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77270830	CTTGTGGAACTCAGA[C/T]TGTATTACATTAGAT	23077
rs189741822	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77203171	AGCCCAAAACCTCCT[C/T]AAGCTGATAAACAAC	23077
rs189749584	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77316892	TGTGGAACACAGCCC[C/T]ACCTCCTCCACATGA	23077
rs189752332	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77184226	TTTAAAATTTCCTTT[A/G]TAACTTCTTCTTTGA	23077
rs189772603	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77309321	GAGGCAGTTTGTGAG[C/T]GACAGTATGTTCACG	23077
rs189779365	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77096870	TAGACAAAGAAAAAA[A/G]TTAACCAAATTTGTA	23077
rs189788419	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77296926	TTGAATTCTGCAAAA[A/C]CATAAACTTAAAACA	23077
rs189790813	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77257278	AAATGGGATGGTTAG[C/T]TGGCACAAAAATATA	23077
rs189795332	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77278351	TTGTTTGCCCCCCGC[C/T]TCATCATACTAATTG	23077
rs189796189	snp	A/G	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77210761	AATATAAACAGGATT[A/G]ATGACAGACTAAAAA	23077
rs189798003	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77056495	TTGCCAAAACAACTT[C/T]CTACTTGCTGACTAC	23077
rs189812383	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77142397	AGCAAAGGCTGCTGG[C/T]GAAGGTCTCTAGAAT	23077
rs189813861	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77208460	TATCGTAATATTAAA[A/C]AAAATCTAAAATGTT	23077
rs189818764	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77172915	TCTAGACAATTCAGC[A/G]TCTCAGTTCCATCAT	23077
rs189831029	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77103889	GTTTTGTAGATCCTA[C/G]TTCTGATATCAAATC	23077
rs189831378	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77169180	TTGGGAGGGCGAGGC[A/G]GGCGGATCACGAGGT	23077
rs189841756	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77125813	TTATTTAGGTTGAGA[A/G]TATCCATAGTGTAAC	23077
rs189845799	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77102565	TGTTTCAAAAAACCA[A/G]AAACATATTTTTAAA	23077
rs189852043	snp	C/T	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77072255	GAGATTGCACCACTG[C/T]ACTCCAGCCTGGGCG	23077
rs189852704	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77236497	TCTATCCTAAAGAAA[A/G]CTCTAAAATATTTTT	23077
rs189884110	snp	A/G	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77249886	TTATCCTTTGATAAA[A/G]ACGACTTTATTGCTT	23077
rs189906828	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77312854	AAGGTTCTATACTAG[C/T]TGCCTAAGAGGAGAA	23077
rs189923686	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77321042	TGGTGATAGTTTCAG[G/T]ACTCTTCAAATGAAC	23077
rs189930585	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77140522	ACCAAAATGCCTGTA[C/T]TTACTCTTTAGATTT	23077
rs189935868	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77292819	AAAAATTAGCTGGAC[A/G]TGGTGGCTGGTGCCT	23077
rs189939709	snp	A/C/T	0.00159649	0.0282165	intron-variant	MYCBP2	GRCh38.p7	13:77254422	ATGGTAGAGACACAA[A/C/T]TTTTTAATATTTCAA	23077
rs189948895	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77273808	TTTAGTTTCTTTCTA[A/G]TTACTCTCTTCCCCA	23077
rs189967543	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77251088	AGTAGAGTATACTCC[A/G]GAATGATTTTGCAAA	23077
rs190013400	snp	A/T	0.00597247	0.0543191	intron-variant	MYCBP2	GRCh38.p7	13:77265503	TGACAATTATCAGAT[A/T]AAAAAAGTATGTTTT	23077
rs190031652	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291039	ATAAATGGAGACATA[C/T]ACCATGTTCATGGAT	23077
rs190049794	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77233018	GTATCACTTTCAGAA[C/T]GTTCTTTCTCCTCAG	23077
rs190059305	snp	A/G	5.21055e-05	0.00510392	intron-variant	MYCBP2	GRCh38.p7	13:77191641	ATTCCTCTAACAAAA[A/G]TAAGTATTGCTTAAG	23077
rs190077633	snp	C/T	0.0236746	0.106192	intron-variant	MYCBP2	GRCh38.p7	13:77122476	GGAGGCCAAGGCAGG[C/T]GGATCACGAGGTCAG	23077
rs190084435	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77151335	CACAATCTCAGCACA[C/T]TTTAAAGCACTAATG	23077
rs190093393	snp	A/T	1.64912e-05	0.00287147	synonymous-codon, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77083130	GTGTGGTAAAGGATG[A/T]GCAGCTTCCCCGGCA	23077
rs190106837	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77300646	TGAGTATGCAACACA[G/T]ATAAAACTATTCAAA	23077
rs190125777	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77065005	TCAAGGGCAATTACT[C/G]TCACATCTGATAAAA	23077
rs190131414	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77063916	AAATTGACTTTTTCC[A/G]CCCTAGGGATATATA	23077
rs190134612	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77083828	AAAAATACCATAAAA[A/T]GTCTCCCTGTCTCTA	23077
rs190151309	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77049477	TGGAAGCAACTTTCC[C/T]TAGTCTCTACCCTCA	23077
rs190159968	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77069977	TATGAACAATATAGC[A/G]CTATTTCCTCACCTG	23077
rs190163272	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77105076	TAGAACGGTGGCAGC[C/T]TCTGAATGGAAGAGT	23077
rs190197121	snp	A/C	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77178672	AATTTTGGGAGACTA[A/C]ATAGATACAAAAATG	23077
rs190208934	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77129260	TTAAGAAAGAAAAAT[A/G]TCAACAAAGAAAGGG	23077
rs190211172	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77158329	CTCAAAAATAAATGC[C/T]TTGTCAGAGATCTGC	23077
rs190215531	snp	C/T	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77110247	ACCCTAAGAAAAGAA[C/T]TGCATTCCTGGGGGG	23077
rs190225325	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77138186	TGATCACATATCTTC[C/T]TTCTCTTTCTTGCTC	23077
rs190278511	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77246917	TTTGACAAAATTCAA[C/T]GCCCTTTCATAATAA	23077
rs190324993	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77315623	CAGCAAGCCGGGTGC[A/G]ATGGCTCACGCCTGT	23077
rs190341633	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77193338	TTCTTTAGATTTACT[C/G]TTTTGTTTTCAAAAG	23077
rs190347780	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77259135	CTGGGTGTTGTGGCA[C/T]GTGCCTATAATCTCA	23077
rs190352670	snp	C/T	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77174622	ATAATTAAATAAGTT[C/T]TTAATGAATCAAACA	23077
rs190352869	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77195211	TATTCTCAACAGTCA[A/T]TGGATTCCCTTTGTC	23077
rs190353881	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77204911	TGTGGGGTGGGGGGA[C/G]GGGGGAGGGATAGCA	23077
rs190357207	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77221743	TCTTCTGTGTCCCAA[C/T]TCTCAAATGAGAAAC	23077
rs190361476	snp	C/T	0.00438332	0.0466095	intron-variant	MYCBP2	GRCh38.p7	13:77152159	GTAGTTTGAGACTTT[C/T]GCTATTTATATAATG	23077
rs190367575	snp	A/C/T	0.00279242	0.0372774	intron-variant	MYCBP2	GRCh38.p7	13:77153697	AAAAAAAAGTTATTC[A/C/T]TGTATTTCCTATGTG	23077
rs190374005	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77184542	TGTTCAAATCTGCAT[C/T]GCTGATGTTTTTGGC	23077
rs190375602	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77133267	ATGAGAATTATAATA[G/T]GCTTAACATCACAGG	23077
rs190387125	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087204	TTACTTTCATTTTAC[A/G]GACATGGAAACCGAG	23077
rs190401356	snp	A/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77302517	ATCCATGAAAGCTGA[A/T]ATAATTCACATAAAG	23077
rs190409421	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77282968	TAACACTCTCTAGAC[A/C]ACTGCAATAACTGCC	23077
rs190425590	snp	A/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77236160	AAGAAGCCTCAGCTA[A/T]GGAAACAGTAAGATT	23077
rs190430464	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77263015	TCACTATTAAACCTG[C/G]AGTGGCATGGCAAGC	23077
rs190438911	snp	G/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77310573	AATATGTCATATATA[G/T]GATTATAGACACATA	23077
rs190439112	snp	A/G	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77225079	GAAAGTAAATTTGTT[A/G]ACATACATTTATCAC	23077
rs190440208	snp	G/T	0.00438332	0.0466095	intron-variant	MYCBP2	GRCh38.p7	13:77214597	TATATTTATGTACAG[G/T]CACATGTCACTTAAT	23077
rs190447280	snp	A/G	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77245360	GGAACCAACCCAAAT[A/G]CTCATCAATGATAGG	23077
rs190453115	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77132448	TCAACTCTACTTCAA[A/T]TCTTTCAGGTTCCAA	23077
rs190461019	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77114227	CATTTGTCCCTTTCT[A/G]AATTCCTTCCTGCAA	23077
rs190466383	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77093461	AGCATTAAAATAATC[A/G]TAGATGTAGGTAGGT	23077
rs190466970	snp	C/T	0.000280174	0.0118325	missense	MYCBP2	GRCh38.p7	13:77125347	TTGCCATCTTCATGT[C/T]GGAGGTACTGGTTTC	23077
rs190472011	snp	C/T	0.00835141	0.0640778	intron-variant	MYCBP2	GRCh38.p7	13:77046654	ATAAAAAGTAAGTTC[C/T]GTACAAGAGTAAGAC	23077
rs190487797	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77238644	CCTAAAAAGATAAAT[C/T]AAAAAAATTAACTAG	23077
rs190496917	snp	C/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77054077	ATGTTACAGAGGAGG[C/T]GAAACCTGAGCTGAA	23077
rs190507343	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77073749	ACTAGAAATGAACAA[C/T]TGGAAAGTGAAATAA	23077
rs190520770	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77197399	ATTTCCGGCCTATGT[A/G]TCAAGCATATGGTGG	23077
rs190534500	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77152551	CCCTGCCCCCCTACC[C/T]TATGCCCCTATAAAT	23077
rs190568766	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77277058	GAATAAAGGAAAGAA[A/G]GTATGTACAGAATGG	23077
rs190579477	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77314642	GGAGCACAGATGATA[C/T]TGAGGGCAGTGAAAA	23077
rs190590535	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77241964	ACATTTCTAATCAAA[A/G]TTTTGCCTATTGGAG	23077
rs190595009	snp	A/C	0.0696718	0.173152	intron-variant	MYCBP2	GRCh38.p7	13:77307643	AAAAAAAAAAAAAAA[A/C]AAAAAAAAAAACTTC	23077
rs190597076	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77099805	AAACAGGATGAAAAG[A/G]AGAATCACCTCCCTT	23077
rs190609947	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77173571	CTATCTACGTAGGCA[C/T]CATCCCTAGACTCTT	23077
rs190618997	snp	A/C	0.0103295	0.0711199	intron-variant	MYCBP2	GRCh38.p7	13:77199751	TGACCCTCCAGCAGC[A/C]TAACTGGGAGGCACC	23077
rs190621287	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77131869	GATAATCTTTCATGG[A/C]GTAGAAAAGAGACCA	23077
rs190637587	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77069314	GTAGTTCATTGAAAA[G/T]AATAATAGTGTAGAA	23077
rs190639361	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77218976	ATGTAAGGAACAGAA[C/T]TGATGAAACTTGGCA	23077
rs190639830	snp	A/C	0.00478085	0.0486577	intron-variant	MYCBP2	GRCh38.p7	13:77277345	CTATCATAACAATAA[A/C]CAACACGGTGCTTGC	23077
rs190650407	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77256980	AGATTTGGAAGCAAC[C/T]TAAGTGTCCATCAAC	23077
rs190666334	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77238916	ACCTGAGGTCAGAAG[C/T]TTGAGACCAGCCTGG	23077
rs190667975	snp	G/T	0.0126979	0.078662	intron-variant	MYCBP2	GRCh38.p7	13:77180453	CTACAAATCTTTCTG[G/T]TTATATGTGGAGCCA	23077
rs190679477	snp	C/T	0.00874735	0.0655527	intron-variant	MYCBP2	GRCh38.p7	13:77197845	CCACTCACTGGATAA[C/T]TGAATACAAAAGGCA	23077
rs190681284	snp	A/C	1.66056e-05	0.00288141	intron-variant	MYCBP2	GRCh38.p7	13:77217828	ATTATTAATGTTTTA[A/C]AAATTCCTTACAGAA	23077
rs190681892	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77138815	TAACATACATTTATA[C/T]ATGTTTTTGAATGTA	23077
rs190705990	snp	C/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77288850	CTTAATTTTCATCAG[C/T]TCATTTCATTCTCAT	23077
rs190710503	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77146134	GACAACACATGTTTT[A/G]GTTATACTTTGAGAA	23077
rs190730626	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77067212	TTTTAAAAAGAAATG[C/T]ACATAAAGCTTTAGT	23077
rs190744833	snp	A/G	0.00755907	0.0610114	intron-variant	MYCBP2	GRCh38.p7	13:77256576	GTGAAAAAGTTCTGA[A/G]TAGACATTTTTCAAA	23077
rs190749499	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77217562	ACAGAATTAGCTCTA[C/T]TGAATGCTTAAAAGA	23077
rs190779751	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77177663	TCAGTGATTGATCTA[C/G]TAAACCCCTGAACAT	23077
rs190782726	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77261823	CAAACCTTCAATTTG[A/T]AAAAAGAGCAATTAT	23077
rs190803718	snp	C/T			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77084746	TCTCAGCTTACAATT[C/T]ATTTCCACTGCTAGA	23077
rs190811479	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77325972	ACTCCTCTTGGTGAA[A/G]GGCAGATTGAAGGGA	23077
rs190812078	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77224622	GTGTAATTTTCACTA[C/T]TTAAGATTTATAGAA	23077
rs190836472	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77295238	CTCCCGGGTTCAAGC[A/G]ATCTCCTGCCTCAGC	23077
rs190842560	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77119385	ATAATAAAGTTTCAT[A/G]TGTGAAAATTTCAAC	23077
rs190845775	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77165942	AAAGTGGTTTACGAA[C/T]TCTCTTACAATGAAG	23077
rs190858510	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77302121	AGAGAGAAAAAAGAA[C/T]GGAACAAAAGCAATA	23077
rs190860117	snp	A/C	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77143427	TCCCTTGACATTTGA[A/C]CTCCAGGGTCCCCAG	23077
rs190866503	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77123138	ATAGTGCCAAATCTT[C/T]GTACTTCCATATTAA	23077
rs190871908	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77105878	ATGGTTCTTTATGGG[A/T]CATTTTGTTTTCTTT	23077
rs190897797	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77239964	TGGAGAATATTTAGG[A/C]AACAAATTGTAAAGA	23077
rs190898060	snp	G/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77198191	GCCAAACTACTATTT[G/T]TCTTATTATCAAAAT	23077
rs190917569	snp	G/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77158639	TTTTTGTAGAGATGG[G/T]GTCTTGCTATGTTGC	23077
rs190952242	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77307744	ACTTTCTAGTAGCCA[A/G]TTCAACTGCCCATCT	23077
rs190997414	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77209450	AAACAGTAAAACATC[A/C]ATTTACACCTAAGTC	23077
rs191012788	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77053562	ACTGCTTACTCCAGC[G/T]GTTTCACTTTTCTAT	23077
rs191013646	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77311733	CTCATCTGAAAAACA[C/G]AGAAAAAAAATTGAT	23077
rs191043767	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77282134	CTGAATGTGAGGCCG[A/G]GTGTGGTAGCTCACA	23077
rs191044302	snp	A/G	0.0182019	0.0936463	intron-variant	MYCBP2	GRCh38.p7	13:77287167	GCTGGGATTACAGGC[A/G]TGAGCCATTACGCCC	23077
rs191047195	snp	C/T	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77058855	CCAGGCATGGTGGCG[C/T]GCGCCTGTAATCCCA	23077
rs191047552	snp	C/T	0.00478085	0.0486577	intron-variant	MYCBP2	GRCh38.p7	13:77245068	AGAAAACATGTCACG[C/T]CAGTTACAATGGTGA	23077
rs191053043	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77328971	TCAACCATCACAGGC[C/T]CCTAGCACAGGGTCT	23077
rs191062815	snp	C/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77247982	AACATCACACACCGG[C/G]GCCTGTTGTGGGGTG	23077
rs191077808	snp	C/T	0.00839839	0.0642547	intron-variant	MYCBP2	GRCh38.p7	13:77267798	TTAACATGCACATTT[C/T]TTAAAATTGCTTGTG	23077
rs191077988	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77181120	GATAAGAAAATTCCA[A/G]CCCCTACCGGTAGAA	23077
rs191079853	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77230102	CAGTCTATATACTCT[A/G]CTTTGCCTTTAGTCA	23077
rs191080016	snp	G/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77198536	ATTGAAATTCAGGCA[G/T]AAACTATAGTTTTCT	23077
rs191124252	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77322260	CTAACAAGAAAGAGA[C/T]AAAGCAGCTGAAAAA	23077
rs191134731	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77150112	TCTGAAGATAACTAA[A/G]ACATCCAAAATATAT	23077
rs191164132	snp	G/T	8.0048e-05	0.00632595	intron-variant	MYCBP2	GRCh38.p7	13:77118320	ATGCTTGATGAGGCA[G/T]GTAAGGCTGACAGAC	23077
rs191171952	snp	A/C	0.00835141	0.0640778	intron-variant	MYCBP2	GRCh38.p7	13:77047679	TGCCCACGGCTGCAC[A/C]GACAGAAAAACCTTC	23077
rs191178777	snp	C/T	0.00199481	0.0315187	intron-variant, nc-transcript-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076929	CTCATTAGCTGATTC[C/T]GCAGGTTTTATAATA	23077
rs191218551	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77054728	GCCTCAGTCCCCCAA[A/G]TAGCTGGGACTACAG	23077
rs191234846	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77122580	TGTAGTCCCAGCTAC[A/T]CAGAGAGGCTGAGGC	23077
rs191244562	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77082470	GCATTCCATCAATCT[A/G]TTTCTTGTATACATT	23077
rs191263685	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77280648	ATTGAACCTTGCCAG[A/G]AACAGTAAGACTGCC	23077
rs191274542	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77320586	AAAAGGCATTCACAA[C/T]GTGCTCAAATTTTTA	23077
rs191281085	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77298897	AGGGCATGATGAATG[C/T]CTATTTCAACTGTGT	23077
rs191286667	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77190514	GTTAGTCAGTAAAAT[C/G]AAAGAACTGAACGTG	23077
rs191294998	snp	A/C	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77170664	TCACTGCAGCCTCCG[A/C]CTCCTGGGTTCAAGC	23077
rs191302278	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77150629	TAATATCCATCAAAT[G/T]CTCTTTGGACTTACA	23077
rs191302334	snp	A/G	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77103140	ATGACTGAGACGAAC[A/G]GAAACATCTTTAATG	23077
rs191308090	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77129956	GCAGAGCATTTAGGA[C/T]CTCTAAGTTTAAGTC	23077
rs191309273	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77201971	TGACACCCTAACATC[A/G]TAATTAAAGGAACTA	23077
rs191316880	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77111392	GAGCATAAAAGTAGA[C/T]GTCATTTGAGACTGG	23077
rs191317485	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77165487	TCTTTTATCACAAGA[C/T]AGGTAAAAACACAAA	23077
rs191328004	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77093769	TGCTTATTATTTCTT[A/G]CACAGACCACTGAAA	23077
rs191337984	snp	C/G	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77273403	AGCAGAATTCCTATT[C/G]ACAGAAATTGAGACG	23077
rs191353980	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77230842	TGGGACTGCAACCTG[C/T]CACAGGAGGTCAGGT	23077
rs191363128	snp	C/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77248698	CCGCTGTGAAAAATA[C/G]TATGGCAGTTCCTCA	23077
rs191367340	snp	G/T	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77210252	GGCTGGAGTGCAGTG[G/T]TGCGATCTCGGCTCA	23077
rs191371725	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77244201	AAATACACACAGATT[C/T]GACTATCATCAAAGT	23077
rs191409219	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77059841	CTATCTGAAGCCAAA[A/T]ACACTCTCGACTAAT	23077
rs191428888	snp	A/G	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77185783	TAAATGCAGCTGGGG[A/G]GCATAAACTCTCAGT	23077
rs191437691	snp	G/T	0.00557542	0.0525036	intron-variant	MYCBP2	GRCh38.p7	13:77252520	GGAGAACAAATCTGT[G/T]GGAGTCAAGTAATTA	23077
rs191445237	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77168106	TGTTAGTTCAAAAAA[C/T]ACAATTTAAAATTGT	23077
rs191449508	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77145621	TCTAAATTCTATGGA[A/G]GTGATCTCTCCAAAG	23077
rs191449695	snp	A/C	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77214033	GAAACACATGCCCCC[A/C]AAAAGAAAGTTAACC	23077
rs191461165	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77124950	AAGACAAAATGCAAT[C/G]AAATGAAGTTGCCTG	23077
rs191467595	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77074538	TAATTGGTAAAAGAC[C/G]TGCAAAGATCTGTAT	23077
rs191468861	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77144166	CAGGGGAGAGACAGG[G/T]TAACAGCAGCGTGGA	23077
rs191469291	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77107975	TTACATAAATGTTGG[C/T]ATACTAAAAGAATTA	23077
rs191472864	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77174096	TGATATTGAAGAAAT[A/G]ACAGCAAAAATATTT	23077
rs191495574	snp	A/C	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77322467	CAAAACCTTCCATTT[A/C]TTTTTTCTTTAACCC	23077
rs191505214	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77255547	TTCATATTATATATT[A/T]AAAAAACCCGATTCT	23077
rs191506813	snp	C/T	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291659	GTAATCCCAGCTCCT[C/T]GGGAGCCTGAGGCAG	23077
rs191509196	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77283686	CAGACTGCTTGAGCT[A/C]AAGAGTTCGAGACCA	23077
rs191517375	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77275301	TCAAATTCTTTAACA[C/T]GGCATGTAAAGCTCT	23077
rs191517948	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77206451	TTAAATAATTGGGCA[C/T]ACATAAATCTTTGAT	23077
rs191519342	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77237868	TTTAAAAAGAGACTT[C/T]TATGTGTCACTGGAA	23077
rs191519559	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77324247	AGAGGCTACTGTTTC[A/G]TGATTTTCTTCTTAA	23077
rs191521162	snp	G/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77303153	GCCTCACCAACATGG[G/T]GAAATACCGTCTCTA	23077
rs191523958	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77225747	AAGATAGACTATATA[C/T]TTCCATTTGCAAATA	23077
rs191527505	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77223675	TTCTGCCATTCTCAG[C/T]ACACAGTCTCCAACT	23077
rs191554491	snp	C/G	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77183733	ATTTTTGTATTTTTG[C/G]TAGAGACTGAGTTTT	23077
rs191556792	snp	A/C	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77114692	GTACTGTCTTTTGAC[A/C]TATATCATATATTTC	23077
rs191562753	snp	A/G	0.00438332	0.0466095	intron-variant	MYCBP2	GRCh38.p7	13:77142766	AAACCCCAAATCCAA[A/G]ATGATCTAAAATCTA	23077
rs191591854	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77292205	ATGAAAGCTCAGTCA[A/G]TGAAGAACTAGGAAG	23077
rs191596411	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77296182	GTCAGTACTTTGGGA[A/G]GCCGAGGTGAGAGGA	23077
rs191598423	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77230407	AGAGAAAAATATATG[C/T]AGAAAAAATACTTAT	23077
rs191606484	snp	C/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77189620	AACATTTTTCAGTAA[C/T]GGTTTATATCCATTT	23077
rs191674848	snp	A/G	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77268290	ACAAGTATTGAGTTT[A/G]CTATTTGAAAATGAA	23077
rs191703068	snp	A/C/T	0.000731568	0.0191117	intron-variant	MYCBP2	GRCh38.p7	13:77166599	ACAGATATATATATA[A/C/T]ACAAACATACACATC	23077
rs191707318	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77235484	TATATGTGATGGAGC[A/G]AAAGTCTTGGGAAAT	23077
rs191709696	snp	A/G	0.00874735	0.0655527	intron-variant	MYCBP2	GRCh38.p7	13:77193676	ATAAACTCCCAAAAG[A/G]TTTCAGTAAAGCTAG	23077
rs191725803	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77123969	TGATTTACATCAAGC[A/G]GAACCCTTATCTTTT	23077
rs191772609	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77272818	AGGCATCCCTTCCAC[C/G]TGCCCTAGGGTTGCC	23077
rs191830936	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77318331	TCATAGGCCAAAAGA[A/C]ATACCAAACAGTAGT	23077
rs191842244	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77196577	AAGTGGAAACGATAA[C/T]ATTTGCTCCCGAAGT	23077
rs191850107	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77215760	CCCAGCTAATTTTTT[A/T]AATAGAGATGGGGTC	23077
rs191857318	snp	C/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77175778	CCAGCCTGGTCAACA[C/G]AGTGAAACCCCTCTA	23077
rs191862114	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77156337	CTTCATTTCCAACTC[A/G]GTGATAATCATGAGT	23077
rs191866883	snp	A/G	0.00557542	0.0525036	intron-variant	MYCBP2	GRCh38.p7	13:77248186	ACAGTAACCCTTCAC[A/G]ACACTAGATTGGGAA	23077
rs191869858	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77124542	TGTATTACAAAACTT[C/T]ATGAGCAACTAGTAT	23077
rs191878628	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77106943	CAAGAGCTTGAGGAG[G/T]TTTTATAAATAAGTC	23077
rs191882022	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075173	TGATCATACCACTGC[A/C]CTCTATCCTGGATGA	23077
rs191900764	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	MYCBP2	GRCh38.p7	13:77045104	ATCTATAAATGTCCA[A/G]TGCTTCACAGGCCAA	23077
rs191910101	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77209860	CTCTATTTTGGAACA[C/T]GGAAGAAAATTACCA	23077
rs191911784	snp	C/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77066515	GATGTTATCTGCATA[C/T]TGTCATGGATTGGCT	23077
rs191913845	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77170307	TTAACATTTTAGTCA[A/G]TTATCCATGAACATG	23077
rs191923006	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77085951	CTCACATTGTAACTG[C/T]AGACTGTCCTATTTT	23077
rs191939362	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77154975	TGTGTATGTATATAT[A/G]AAGTATATTATATGT	23077
rs191946690	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77135306	TTCATTTACTTTAAA[C/T]GAACTGAAGTAAGAA	23077
rs191954838	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77287939	TGATCTCCCTTCCTG[C/T]GCTTTCCAGTGAATT	23077
rs191956493	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77115800	GTTAACCAGGATCTT[C/G]AGTTATGACATTCAG	23077
rs191960949	snp	A/G	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77113076	TACACTGCCTGACAC[A/G]TAGGTGGACTCAATA	23077
rs191967706	snp	A/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77095279	AAAGTGTAGGTCAAA[A/T]ACCGAACTACCCTAG	23077
rs191985487	snp	A/G	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77056212	AGAAGTGAACAGGTA[A/G]TATTTGCTGTAAAAC	23077
rs191986532	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77048606	CTCAATCTCAGTGTA[C/T]GTTCTTAGGCCAGTT	23077
rs191997873	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77088559	ATGACATTCTGAGTA[C/T]AAAAAGCTTTTAAAA	23077
rs192059739	snp	A/T	0.000441762	0.0148555	intron-variant	MYCBP2	GRCh38.p7	13:77169576	TTAAAAAAGATATTT[A/T]AAAAAAACATTCAAA	23077
rs192061269	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77226104	TTTATTCAATATATT[A/G]CAGTTCAATGGCCTA	23077
rs192070196	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77246668	GGAGAGGGGCAGGGG[A/G]AGGCAAAAAAAAAAA	23077
rs192072483	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77127527	TACAGTAATATGAAC[A/T]CTATAATTTATTTCA	23077
rs192080162	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77207027	TTTGAAAATAGTAAC[A/G]TAGATTATAATACTT	23077
rs192098689	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77172973	TACCTCCTGGGGTTA[C/T]TGTGAGGACAAGGTG	23077
rs192099040	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77199065	AATAGGAACAGCTCC[A/G]GTCTACAGCTCCCAG	23077
rs192099836	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77240834	AATTGAGGTTCATAC[C/T]GAAGATTCCACTCAA	23077
rs192101430	snp	A/G	5.25767e-05	0.00512695	missense, utr-variant-5-prime	MYCBP2	GRCh38.p7	13:77278907	CAAAGGCCAACCTCA[A/G]TAATCTATTTAAAAG	23077
rs192103918	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77151448	CTTATACCTAAAGCC[C/T]AAATATGTTTCTTTA	23077
rs192103944	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77220875	TAGGCACAGTATATA[G/T]GTATGACTACTGCAT	23077
rs192112697	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326041	CACGTGCAAATAACA[C/T]TGCGGCAGAGACACT	23077
rs192118702	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77303916	AGCAGACATTCAATA[A/G]AGGTTATCAGGGAGC	23077
rs192119226	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77297753	CAGATGAAAATGTTA[C/T]CCTTGACATTGCCTT	23077
rs192120439	snp	A/T	1.65471e-05	0.00287633	missense	MYCBP2	GRCh38.p7	13:77181779	CTCTGTACTAACTTG[A/T]TTAACAATTGATCGT	23077
rs192124444	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77160692	AGTGCTCTACAGATA[C/T]TATTTAAATCACTAT	23077
rs192136972	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77264661	TTTCATCAATACTGC[A/C]TGTATCTCCATAGAA	23077
rs192152030	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77298278	ACCACTACTTATCTT[C/G]GAGGTCTCAGCATAA	23077
rs192153107	snp	G/T	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77284833	GTCACTACAACCCTA[G/T]GAGGTAGATGCAACC	23077
rs192159106	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77279464	TAAAGATTGAGAGAG[A/C]AAATTGCAATGAATG	23077
rs192175560	snp	A/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77258158	CTAAGCACAAAGGAG[A/T]CCATAAATAATTTAT	23077
rs192184659	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77141223	AAAATGGAAAATAAT[A/T]AAAAAAAGAACCCTT	23077
rs192185448	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77065246	AAATATTTTAATTCA[A/G]TGAACACCCTGAGAA	23077
rs192191668	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77092897	CTCAAAGTAACCCTT[C/T]CCTACTCTGATTTAC	23077
rs192196792	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77241230	ATGTCAAGTTATCAA[C/T]GCACGATTCAATGTT	23077
rs192216909	snp	C/G	0.00438332	0.0466095	intron-variant	MYCBP2	GRCh38.p7	13:77070373	GAATGTGGCCCAACA[C/G]AAATTCATAAACTTT	23077
rs192231611	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77258897	AAACAAAAAGAAAAC[C/T]CTTAAATGTTTAGTA	23077
rs192234731	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77221550	CCCTTTCCACTCTGG[C/T]AAGACCATGAAATAC	23077
rs192262023	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77181990	ATCTAAGTTTCTGAA[C/T]ACATAAAAGGTAAAC	23077
rs192327095	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77069575	AAACCCCGTCTCTAC[C/T]AAAAATACAAAAATA	23077
rs192334427	snp	C/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77195489	GTAGTCCCAGCTACT[C/T]GGGAAGCTGAGGCAG	23077
rs192357109	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77308687	GTAGTTATTTTGAGA[A/G]GTGATCCCAGGAAAA	23077
rs192366174	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77154319	TAAGTCAAGGAAAGA[C/T]AGTAGGAGAAGCAAA	23077
rs192371347	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77269704	ACACAAGAACTCTAA[A/G]GAAGGTATGTTTAAT	23077
rs192379650	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77264081	CCTCTGTTGAAGTCA[A/G]AATGAGAGTTCTCCA	23077
rs192387583	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77249747	CAGGAGAATAAATTT[C/T]AATTCCAACATTGTT	23077
rs192387727	snp	A/C	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77289774	TTTACTTGTAAAAAA[A/C]CATGTAGAGAATCTT	23077
rs192387948	snp	A/G	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77303312	TCCTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCC	23077
rs192419939	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77074961	TATCTGTAATCTCAG[A/C]ACTTTGGGAGGCCAA	23077
rs192420879	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77188171	GAAAAATCTTTCATA[C/T]ACTTTTAGGATACTT	23077
rs192428489	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77149357	TCTCTCCAAACCCAC[C/T]GAATCTAAATCTCTG	23077
rs192456079	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77110116	AGGTCTGACTGCCTG[C/T]GGGGTTAGGCAGAAT	23077
rs192484938	snp	A/C	0.00874735	0.0655527	intron-variant	MYCBP2	GRCh38.p7	13:77257503	ACTCATGTACCCCAT[A/C]CATATACCTACTATC	23077
rs192496884	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77219205	AATAAACCACACAGA[A/T]AGAAAGAACTCAAGG	23077
rs192543293	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77314129	AACCTACTCTTAGCA[C/T]GTGATCCCACAATCA	23077
rs192546735	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77061562	CCAAGGTCTTTGATT[C/T]CAAAGTCCACTTTTT	23077
rs192589111	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77121282	ATTTAATAAAGATTT[C/T]TGGGTGAACACAAAT	23077
rs192616523	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77050734	AGTGCTGAACAGCCA[C/T]CTTTTCACCAATCCT	23077
rs192617138	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77159941	ATCTTAAGGTACAAA[G/T]ATTTAACTTTAAAAA	23077
rs192619589	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77139584	AAAAACACAAGGAAA[C/T]CACACTTTAAGATAC	23077
rs192628193	snp	C/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77119642	TTAGATATATTTCAT[C/G]AAGTTTAAGTTTCTT	23077
rs192632536	snp	A/C	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77241714	TTATCAATCAACATC[A/C]CTTATCAGATGCTAT	23077
rs192637843	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77101408	ACCTGCTGATGCTAC[C/T]TCTATTCTAGGAATG	23077
rs192639283	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77268962	GGAAATCTTTATTCT[C/T]TATCCTTATACAAAG	23077
rs192641419	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77231863	ATAACAATTTCATTG[C/T]ATACCCCAAATATTA	23077
rs192657934	snp	A/T	0.00119737	0.0244387	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77080199	CTCTTTTACTTACTC[A/T]ATACCAGGGAGGAAT	23077
rs192663578	snp	A/C/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77199187	CAGTGGGTGTGCGCA[A/C/G]CATGCGCGAGCTGAA	23077
rs192665830	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77051351	GTGGCCTGTCCAAAA[C/G]GTCTGGACAAAGATC	23077
rs192672911	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77161399	TAAAGCAAACAATAA[C/T]AAAAACAACAAATGA	23077
rs192722074	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77214886	CACCTTAGCATACGC[A/G]GTCCATCACTGACCA	23077
rs192723005	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77174964	ATATTATATATATAT[A/T]TTTTTTTCTGAGACA	23077
rs192737929	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77135042	CAATCTCTGCCCCCA[C/T]TCCTCTCTCTATAGT	23077
rs192741610	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77284311	CACACTTAGGAGGAG[A/C]AACAGAGGAACAAAG	23077
rs192756254	snp	C/T	0.00874735	0.0655527	intron-variant	MYCBP2	GRCh38.p7	13:77246228	AGACATAGCTAGACA[C/T]CCTGTGAAATGTGTC	23077
rs192757686	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77097009	TCAATCTAATCTAAT[C/T]TAATTTGCAATTCTG	23077
rs192780322	snp	C/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77246011	GATTGTGAACCATAT[C/G]GGGTATATGTTGACA	23077
rs192782645	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77325367	CTGTGGGAAAAAAAA[C/G]ATGAAGCCAACTCCC	23077
rs192795446	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77205776	TTATCCCTTGTCTGA[A/T]TAATGATCATATTTA	23077
rs192799759	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77136236	TTGTAGTGACTTCCA[C/T]GTGCACTGCACTTCA	23077
rs192845881	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77066159	TGAAAAAGATGAAAA[C/T]GTTATTTCAGAATGC	23077
rs192864384	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77255023	ACTTAAGTTGATTCC[A/G]TATCTTGGTGTTGTG	23077
rs192866534	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77215147	TATAACTTAATTTTT[A/G]GCAACATGTAAATGT	23077
rs192890432	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77102112	AAATGGTAAGCATTC[A/G]TTCACTAAATGACCC	23077
rs192896414	snp	A/C	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77293541	TAATTCCCCAGAACC[A/C]AGGTGAATATTACCT	23077
rs192926561	snp	C/T	0.00438332	0.0466095	intron-variant	MYCBP2	GRCh38.p7	13:77121162	AAGCACTCTCATAAA[C/T]TTAAGCCAAAACTGG	23077
rs192938795	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77269779	GTTGTCCAGTCATAC[A/G]GCTAGTAGGAAGCAG	23077
rs192946069	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77233402	TTTCTTCCAATTTCC[C/G]CACTCCAGCCCCCCA	23077
rs192947227	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77191887	TATTTTTTCAAAATC[A/C]CTTGTGAACAAAAAC	23077
rs192963020	snp	C/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77144859	TAAACCTACTTTCCC[C/T]TGCCTTCTCTCATGG	23077
rs192965703	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77309014	TTGCAGAAGACAGTA[C/T]GCAAATGGATGCCAA	23077
rs192992583	snp	A/G	9.27773e-05	0.00681029	intron-variant	MYCBP2	GRCh38.p7	13:77263632	AAATATAGGGAAAAC[A/G]CTTAATTTGCTATCT	23077
rs192997700	snp	C/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77225303	TAAATACAAAGGTCT[C/T]ACAGATTTGAGAGAC	23077
rs193001913	snp	C/T	0.00835141	0.0640778	intron-variant	MYCBP2	GRCh38.p7	13:77184589	TTACTGAAAGAGGAG[C/T]GTTAAAGTCCCCAGC	23077
rs193002592	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77281125	CAGTTTGAAGTCTTA[C/T]AGTCAATGAAAACAC	23077
rs193003970	snp	A/C/T	0.000798403	0.0199641	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075610	AGCCAATGTCATCTG[A/C/T]AATTTTTTTCACACA	23077
rs193043570	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77320833	TAGCTTCCACTTACA[A/G]GAAATACAGATACAA	23077
rs193045363	snp	C/T	0.029116	0.117091	downstream-variant-500B	MYCBP2	GRCh38.p7	13:77044170	GTTTGAGACCAGCCT[C/T]GGCAACATGGCAAAA	23077
rs193055054	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77085260	CTTGTTATTGTTTTG[C/T]TATCTAATTCTTATA	23077
rs193066441	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77237543	AAATAAGTAAAACTT[G/T]ATTAGAAGATGACAA	23077
rs193068770	snp	G/T	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77046180	CAGTATTTTAAAAAA[G/T]AAAATTATTATATTA	23077
rs193069129	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77274710	ATCTTTCCAATCCAT[A/G]CTATCATCATCTCTT	23077
rs193076959	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77086570	CTTCTGAAACTCCAA[A/G]TAGGTAAGTTGTACA	23077
rs193081116	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77114842	TTTGCCATTTTTCTA[A/C]CACAAACAAATAAAT	23077
rs193082767	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77196446	TGGGGTGAGGACAGA[C/T]GTAGAACACAAGTTG	23077
rs193125571	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77130477	CATCTACATAAATAT[A/G]TACTAATTCATAAAT	23077
rs193128670	snp	G/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77313831	AAACAAACAACTCAA[G/T]TAAAGATGGGGCAAA	23077
rs193143535	snp	A/C/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77210414	AGCCAGGATGGTCTC[A/C/G]ATCTCCTGACCTCGT	23077
rs193149060	snp	G/T	0.00478085	0.0486577	intron-variant	MYCBP2	GRCh38.p7	13:77172370	ACAAGAGTCAAATTG[G/T]GTAAGGTTTGTAGGC	23077
rs193162835	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77140316	CCTCTGCAAATAACA[A/G]TATAACAACACTAAC	23077
rs193170772	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291013	TTGCTGAGTGAAATT[C/T]AAAGACTTAAATAAA	23077
rs193172126	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77250458	ACTCCCCCAAATCAG[C/T]CAATTATTACAAAGC	23077
rs193172911	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77319363	CAAGTGCACTCAGAT[A/G]CCCCATCCTAAGGGT	23077
rs193174613	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77212513	TTAGTATTCCAAATT[A/G]TTCATTTAAAAAGTC	23077
rs193207586	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77259318	TCCATAACCATTCAA[C/T]ACCACTTCCCCAATA	23077
rs193239324	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77066769	GCCAAAGCATCAAAG[A/G]TATTTTGCAATTATT	23077
rs193244858	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77094961	GCACAAGGCTGGTAG[G/T]TGCCCAGTTGGTATT	23077
rs193280209	snp	A/C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77111917	TTACAAGACCCTTCA[A/C/T]GATCCAGCCCCAACC	23077
rs193295145	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77191435	CAAGCTCGTAAACAA[C/T]GTAATACCCAGAAAT	23077
rs193296007	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77071720	AATATTATTGATCAA[A/C]TTGAACTAACTGATA	23077
rs193299926	snp	C/T	8.23676e-05	0.00641693	missense	MYCBP2	GRCh38.p7	13:77150897	GGTTTCTTTGCTTGA[C/T]CTTGTTGTAAAGACA	23077
rs193920951	snp	A/C/G	3.29849e-05	0.00406098	MYCBP2	13	allele_origin=G(germline)/A(somatic)	13:77126432	AGGAGGGCCAGGCAT[A/C/G]TACAAGGTAGTGAAG	23077
rs199501276	snp	C/T	0.000675336	0.0183633	missense	MYCBP2	GRCh38.p7	13:77144528	CAATAAGTCCCATCA[C/T]TATTGACACGGATCA	23077
rs199543488	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77169173	CAGCACTTTGGGAGG[C/G]CGAGGCGGGCGGATC	23077
rs199549924	in-del	-/G	0.0263992	0.111815	intron-variant	MYCBP2	GRCh38.p7	13:77128628	TTCTTGTGCTAAACA[-/G]TATAAAACACTGACA	23077
rs199551229	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77052926	TTGAGCTCAGGAGTT[C/G]AAGACCAGCCTGGGC	23077
rs199552610	in-del	-/G			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087072	TGCTCATGGTGTCTT[-/G]TTTGTGAGTTTTAAG	23077
rs199562220	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77071237	TGTATATATGTGTGT[A/G]TATATATATATATGC	23077
rs199569666	snp	A/G	0.00279162	0.0372561	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77079042	CCTCCAACTAACCAC[A/G]GTTCCTATAACTTTA	23077
rs199589543	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77200129	AACCAAAGGCAAAGA[A/G]GTTGAAAACTTTGAA	23077
rs199591828	snp	A/G	0.00199806	0.0315442	intron-variant	MYCBP2	GRCh38.p7	13:77064781	GACCAGAAATGTATT[A/G]CCATAGTAAACTCTT	23077
rs199599409	snp	A/T			utr-variant-3-prime	MYCBP2	GRCh38.p7	13:77044918	TTTTTTTTTTTTTAA[A/T]TAACAGTCTAGGAAA	23077
rs199599448	snp	C/T	0.000115444	0.00759662	missense	MYCBP2	GRCh38.p7	13:77098905	TGATCAGCAGTAGTC[C/T]GGCTCATACGTCCAT	23077
rs199630456	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77243174	AGCTAGATGATTGGC[A/C]AAAAACAACAACAAC	23077
rs199670865	snp	A/G	0.000613736	0.0175069	intron-variant	MYCBP2	GRCh38.p7	13:77068841	ACACACCTATTTAAA[A/G]TTAACACAGAACATG	23077
rs199676134	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77166976	GACAAAACACACACA[C/T]ACACACACACACACA	23077
rs199679583	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77068935	AAGAATGTAAATTGA[C/T]ACTCAATTTAATACT	23077
rs199704188	in-del	-/TAAT			intron-variant	MYCBP2	GRCh38.p7	13:77144285	AAAATGTTAATGCAC[-/TAAT]TAAATACTCATTATG	23077
rs199708305	snp	A/G	1.64857e-05	0.00287099	synonymous-codon	MYCBP2	GRCh38.p7	13:77166432	TGTCAATTTTGGTCC[A/G]TATCCTGAATTCTGA	23077
rs199751511	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77169870	GTACTATTCTAAAGG[C/T]TTTTGAGAATACATG	23077
rs199820026	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77072322	AAAAAAAAAAAGAAA[C/T]CAAATGGGAATAAGA	23077
rs199829350	snp	C/T	0.000445313	0.014915	missense	MYCBP2	GRCh38.p7	13:77098609	TTTTTTGAGGTAGAT[C/T]TTTATCATGTGGTGA	23077
rs199844133	snp	G/T			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087077	ATGGTGTCTTGTTTG[G/T]GAGTTTTAAGAATTT	23077
rs199846749	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77049295	CCTGCTACTTCTATT[-/A]AAAAAAAAACAGTAT	23077
rs199858534	snp	C/G	0.00010652	0.00729717	synonymous-codon, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326575	GGCCCGGCCTGACAG[C/G]AGCAGCTGGTAGTGA	23077
rs199859615	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77238268	AAAAAAAAAAAAAAA[C/T]AAATATGCCTGGACA	23077
rs199862611	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77108848	AGCTGGGACTACAGG[C/T]GCCTGCCACCACACC	23077
rs199868815	snp	C/T	0.000412109	0.0143487	missense	MYCBP2	GRCh38.p7	13:77261281	GAGAAGTGTACTATC[C/T]TTGGAGATTTTGTAA	23077
rs199871171	in-del	-/C	0.00835141	0.0640778	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77086300	TAACTTGTAATGTTG[-/C]TACCAAAAATTAAGC	23077
rs199880675	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77201691	AAATTATAACAAACT[A/G]TCTCTCAGACCACAG	23077
rs199887178	in-del	-/ATTGT			intron-variant	MYCBP2	GRCh38.p7	13:77307659	AAAAAAAAAAACTTC[-/ATTGT]ATTGAAGTTTTTTAA	23077
rs199897420	snp	G/T	0.0012381	0.0248498	intron-variant	MYCBP2	GRCh38.p7	13:77257833	CAGTTACCAAACCTA[G/T]AGGAAAGAAACAAAT	23077
rs199903393	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77134593	TAACAAAAAAAAAAA[-/A]GGAAAAGTGTTCTAA	23077
rs199915400	in-del	-/AAAAAAAAAAAAAAAA			intron-variant	MYCBP2	GRCh38.p7	13:77301423	GCAAGACTCCATCTC[-/AAAAAAAAAAAAAAAA]AAAAAAAAAAAGAGG	23077
rs199937743	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77223911	CGAACTAAAACTAAA[A/C]CTAAAACAAATGAAG	23077
rs199956144	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77206598	TACTCTAAAAAAAAA[-/A]CCCTGGACAGCACAC	23077
rs199969684	in-del	-/AGG			intron-variant	MYCBP2	GRCh38.p7	13:77246540	AGGAAAAGAAGGAGA[-/AGG]AGGAGGAGGAGGAGC	23077
rs199974362	snp	C/T	0.00199804	0.0315441	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087459	CTATAAAAATATGCA[C/T]AATCAAAACAAAAAT	23077
rs199997994	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77285857	AAAAGGAGAAAGGAA[A/G]GGAAAGGAAAGGAAA	23077
rs200013434	snp	C/T	0.000198705	0.00996559	intron-variant	MYCBP2	GRCh38.p7	13:77121514	CAATAAAAGCCATAG[C/T]TGTAACATTAGTTTC	23077
rs200019716	snp	A/C/T	0.00029868	0.0122171	missense	MYCBP2	GRCh38.p7	13:77169622	TACACACCTTGGGAA[A/C/T]AGCAGCAGCTACTGG	23077
rs200029633	in-del	-/TAAG	0.00993419	0.0697739	intron-variant	MYCBP2	GRCh38.p7	13:77281787	TTATTATTTCATGAC[-/TAAG]TGTGATCATAAAAGT	23077
rs200030860	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77072323	AAAAAAAAAAGAAAT[A/C]AAATGGGAATAAGAA	23077
rs200033933	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77183541	TGATAGTCCCTATTT[C/T]TTTTTTTTTTTTTTT	23077
rs200035013	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77172345	TGAAGCGTGATGGGT[A/G]GGAAGGGAAACAAGA	23077
rs200043974	in-del	-/GG			intron-variant	MYCBP2	GRCh38.p7	13:77056098	ACACGCTCTGTGTTT[-/GG]GGTGTGTGTGTGTGT	23077
rs200056944	snp	A/G	0.000528375	0.0162453	synonymous-codon	MYCBP2	GRCh38.p7	13:77260564	TATCTTTTTAGGTTT[A/G]TAAGGTTTGGATTGC	23077
rs200095232	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77197742	CAAAACAAAACAAAA[A/C]AATACAGAAGGGCTT	23077
rs200099423	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77310786	TGTGTGCGTGCGCAT[A/G]CACACACACACACAC	23077
rs200139496	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77071669	AAAACCAGTAAGGCT[C/T]TTAAAGACTTGAATA	23077
rs200149490	snp	A/T	0.0379877	0.132479	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77292531	AAAGACACCAGATTT[A/T]AAAAAAAAAGAGCAC	23077
rs200152309	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77223908	TCACGAACTAAAACT[A/C]AAACTAAAACAAATG	23077
rs200163933	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77204825	ACACCGCATATTCTC[A/G]CTCATAGGTGGGAAT	23077
rs200173979	in-del	-/ACACACACAT			intron-variant	MYCBP2	GRCh38.p7	13:77166967	TACTTCAAAGACAAA[-/ACACACACAT]ACACACACACACACA	23077
rs200206492	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77302776	GCTATTTTAATATTT[G/T]ACAAAGTAATTTTTA	23077
rs200206870	snp	C/T	0.00199808	0.0315444	synonymous-codon	MYCBP2	GRCh38.p7	13:77176617	ATGAGTTGAATCTCC[C/T]GCATGTTCACTCTAA	23077
rs200219506	snp	A/G	1.64738e-05	0.00286995	synonymous-codon	MYCBP2	GRCh38.p7	13:77125400	CCATGCCTCTCCTTC[A/G]TCACTCTCACAGAAC	23077
rs200227639	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77223915	CTAAAACTAAAACTA[A/T]AACAAATGAAGTAGG	23077
rs200232924	in-del	-/AC	0.00914312	0.0669923	intron-variant	MYCBP2	GRCh38.p7	13:77149934	ATCATCTGCCCAATT[-/AC]ACTGTCCATATTCCA	23077
rs200250987	snp	C/G	0.00199792	0.0315431	synonymous-codon	MYCBP2	GRCh38.p7	13:77144482	AACATGAAGAGTGTA[C/G]AGTCCAATAGCCCCT	23077
rs200275406	in-del	-/T	0.000449809	0.0149901	intron-variant	MYCBP2	GRCh38.p7	13:77206868	CTCAATGTGGTTTTG[-/T]TTTTTAAAAAAAATT	23077
rs200276090	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77311565	GAGAAGTTTTTTTTT[G/T]TTTTTTTTTTTTTGT	23077
rs200311408	snp	G/T	0.000440305	0.014831	intron-variant	MYCBP2	GRCh38.p7	13:77061123	GGCACGGTTTAATCT[G/T]TTTTTGTGGGTTTTA	23077
rs200327011	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77245865	ATACACACACACACA[C/T]ATATATATACACACA	23077
rs200348251	in-del	-/T	0.0146672	0.084371	intron-variant	MYCBP2	GRCh38.p7	13:77103660	ATAAAGATTTACAAG[-/T]TTTTTTTTTAATAGT	23077
rs200361515	snp	C/T	0.000679635	0.0184216	intron-variant	MYCBP2	GRCh38.p7	13:77180322	ATTCTCTTCACTCTG[C/T]GATACATAAGAAAAA	23077
rs200386850	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77154417	AGAGGAAAAAAAAAA[-/A]GCAGATCCATCATAT	23077
rs200393657	snp	C/T	0.00199792	0.0315431	synonymous-codon	MYCBP2	GRCh38.p7	13:77097446	ACAGATGGTATCTTT[C/T]TCTGGTCCTCCTACT	23077
rs200405135	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77072317	AAAAAAAAAAAAAAA[A/G]GAAATCAAATGGGAA	23077
rs200433675	snp	A/T	0.224493	0.248695	intron-variant	MYCBP2	GRCh38.p7	13:77243963	GATCCTAGGGGGAAA[A/T]ACAAAAAAAAAAAAA	23077
rs200444498	in-del	-/T			intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77074007	ATCCCCACCGCCCCC[-/T]CCCCCTTTTTTTTTT	23077
rs200479565	snp	C/G	0.00199792	0.0315431	missense	MYCBP2	GRCh38.p7	13:77098954	TGTGTTTAGAGGACA[C/G]CTCTGATTTTCCTGA	23077
rs200480392	snp	A/G	0.0028173	0.0374261	intron-variant	MYCBP2	GRCh38.p7	13:77095622	CGAAGAAAAAAATCA[A/G]ACTAATCTTTTCTGA	23077
rs200496039	snp	A/T	0.0391387	0.134304	intron-variant	MYCBP2	GRCh38.p7	13:77267404	AACATAAAATAAAAT[A/T]AAATAAAATTAAATT	23077
rs200548331	snp	A/C/T	4.95111e-05	0.00497525	missense, utr-variant-5-prime	MYCBP2	GRCh38.p7	13:77225488	AGCTCACAGTCAAAT[A/C/T]GCACAGAGCCTGGAG	23077
rs200563433	snp	A/T	0.00476192	0.0485622	intron-variant	MYCBP2	GRCh38.p7	13:77055554	AGTATAATTTATAGC[A/T]TACCTTTCTGCATTT	23077
rs200669454	in-del	-/TA	0.0471551	0.14613	intron-variant	MYCBP2	GRCh38.p7	13:77245836	TAATACATATATATG[-/TA]TATATATATATGTAT	23077
rs200679288	in-del	-/T			intron-variant	MYCBP2	GRCh38.p7	13:77195035	GTCCTTTTTTTTTTT[-/T]AAGAAAACCTTTTTC	23077
rs200679589	in-del	-/T			intron-variant	MYCBP2	GRCh38.p7	13:77250239	AAAAAAAAAAAAAAA[-/T]CATATCTCAGCAGCC	23077
rs200685646	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77153751	ATTTCCTTAAAATAA[A/C]CTTTTTTTTTTAATT	23077
rs200687911	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77186801	CGAGTTTATAGATTC[A/T]ATTTTTTTTTTTTTT	23077
rs200690773	snp	C/T	0.00199802	0.0315439	intron-variant	MYCBP2	GRCh38.p7	13:77205466	TCCTAAACCGAAGTA[C/T]ACATACTTTCAAACC	23077
rs200731545	snp	A/G	0.0370032	0.130891	missense	MYCBP2	GRCh38.p7	13:77098674	GACCTATTGGCTGGG[A/G]GAGTCTTTGGCTTAG	23077
rs200747205	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77160269	CACCAAACTGCCAGC[A/G]AACAAATCCCAGTGC	23077
rs200748233	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77109941	TTTACTTTAATCTCT[C/T]AATCCTGTTATCTTT	23077
rs200776219	snp	C/T			missense, utr-variant-5-prime	MYCBP2	GRCh38.p7	13:77288175	CCTTTGGAAGCTTGA[C/T]AGGGGGCTCTTTGGA	23077
rs200791802	snp	G/T	0.142987	0.225939	intron-variant	MYCBP2	GRCh38.p7	13:77070727	CTTTACATAGAAAAA[G/T]AAAAAAAAAAAAAAG	23077
rs200803417	snp	A/G	8.25498e-05	0.00642402	synonymous-codon	MYCBP2	GRCh38.p7	13:77251156	TGTCTCTTACCCTCC[A/G]GGGACTCTGTCTGGC	23077
rs200851216	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77219821	CCGAGAGCAGGAGTT[C/T]TCAACTCAGATATAA	23077
rs200851938	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77303772	TAAATGCATATACTG[-/A]AAAAAAAAACACTGA	23077
rs200865918	snp	G/T	1.651e-05	0.0028731	synonymous-codon	MYCBP2	GRCh38.p7	13:77096321	AAATACCTTCTCCCT[G/T]GCAGCAGCCTGTTTT	23077
rs200876431	in-del	-/A	0.0232847	0.105357	intron-variant	MYCBP2	GRCh38.p7	13:77308187	CCTCCCCTACCCATC[-/A]ACTCAGAGCAGAGAA	23077
rs200910560	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77311579	TGTTTTTTTTTTTTT[G/T]TTTTTTTTTTAAAGA	23077
rs200915072	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77131517	ACACACACACAAACA[A/C]ACACACACACACACA	23077
rs200915979	snp	A/G	0.000307953	0.0124049	missense	MYCBP2	GRCh38.p7	13:77058297	TGCTTCAGGCTTGTG[A/G]CACTTTTGTCACAGC	23077
rs200921734	snp	C/G	0.00299544	0.0385843	utr-variant-3-prime	MYCBP2	GRCh38.p7	13:77045327	ACTTCACCGCATCCT[C/G]TTGGGGGATGAAGGC	23077
rs200925861	snp	A/G/T			intron-variant	MYCBP2	GRCh38.p7	13:77223913	AACTAAAACTAAAAC[A/G/T]AAAACAAATGAAGTA	23077
rs200927936	in-del	-/T			intron-variant	MYCBP2	GRCh38.p7	13:77249279	CAATTTTATATGTAC[-/T]TTATCATAATAAGAT	23077
rs200944068	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77234845	TAAGGTAATAATATT[A/G]TTATATTACCATTTT	23077
rs200949024	in-del	-/TT	0.00716266	0.059414	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087070	CTTGCTCATGGTGTC[-/TT]GTTTGTGAGTTTTAA	23077
rs200958716	in-del	-/ACAAACACACAC			intron-variant	MYCBP2	GRCh38.p7	13:77131514	CACACACACACACAA[-/ACAAACACACAC]ACACACACACACACA	23077
rs200961214	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77057640	GGGATAATCTAATTA[C/T]TTCCCCCTGGCTTCT	23077
rs200975511	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77187706	GCAAGCATGTTGTAG[A/G]GCATCCTGTATTTGA	23077
rs201029559	snp	A/T	0.00244964	0.0349116	intron-variant	MYCBP2	GRCh38.p7	13:77058416	GTATTCCTGTTAAAG[A/T]TGAATTACAATGTTA	23077
rs201032324	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77072300	CATTTCAAAAAAAAA[A/G]AAAAAAAAAAAAAAA	23077
rs201035069	in-del	-/T	0.0275645	0.114116	intron-variant	MYCBP2	GRCh38.p7	13:77104019	AGCACTTAATTTATC[-/T]TTTTTTTGAAGAATT	23077
rs201049836	in-del	-/TA	0.0232847	0.105357	intron-variant	MYCBP2	GRCh38.p7	13:77049412	TTTTGAAATGGATAG[-/TA]TATGTTTCACATGGT	23077
rs201071696	in-del	-/TA	0.0209421	0.100162	intron-variant	MYCBP2	GRCh38.p7	13:77262632	TTCAGATTCTCTGCC[-/TA]TGTCTTTTTCTACAG	23077
rs201072926	in-del	-/A	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77156877	TAGTGAGGCTGACTT[-/A]AGTGATTTGACATTC	23077
rs201117052	in-del	-/AT	0.0437281	0.141251	intron-variant	MYCBP2	GRCh38.p7	13:77110014	AATTGATTGTAAAAC[-/AT]GTGTGTTTGAACAAC	23077
rs201118256	snp	A/C	0.0227355	0.104168	intron-variant	MYCBP2	GRCh38.p7	13:77243965	TCCTAGGGGGAAATA[A/C]AAAAAAAAAAAAAAA	23077
rs201119595	in-del	-/T			intron-variant	MYCBP2	GRCh38.p7	13:77202033	GCAGAAGGCAAGAAA[-/T]AACTAAAATCAGAGA	23077
rs201124867	in-del	-/ACC	0.0256215	0.110247	intron-variant	MYCBP2	GRCh38.p7	13:77297888	AGCTAGGTTACCACC[-/ACC]TCTTACCTGGACCAC	23077
rs201140348	snp	C/G	0.000330814	0.0128568	missense	MYCBP2	GRCh38.p7	13:77267903	CTTATGGCTGTCATG[C/G]TGTGGTTATTCACAT	23077
rs201150887	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77223917	AAAACTAAAACTAAA[A/C]CAAATGAAGTAGGGA	23077
rs201166357	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77285867	AGGAAGGGAAAGGAA[A/G]GGAAAGGAAAGGAAA	23077
rs201181392	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77111597	AATTTTTTTTTTTTT[C/T]CTTTTAAGTAGAGAC	23077
rs201198960	snp	A/G/T	1.79855e-05	0.00299873	intron-variant	MYCBP2	GRCh38.p7	13:77176643	TCTAAAAAAAAAAAA[A/G/T]GAAACACAAAAATTC	23077
rs201237819	snp	A/G	0.00199792	0.0315431	synonymous-codon	MYCBP2	GRCh38.p7	13:77098259	GCTAAAATGAACTTT[A/G]TTTGAACCTTCATCC	23077
rs201267307	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77230418	TATGTAGAAAAAATA[C/T]TTATTAAAAGACTGA	23077
rs201282387	in-del	-/C			intron-variant	MYCBP2	GRCh38.p7	13:77218271	CTGTATACTGACTGG[-/C]CTGTTAGAGATCTTT	23077
rs201293964	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77245873	ACACACACATATATA[C/T]ACACACACACAAACA	23077
rs201311103	snp	A/G	0.0125049	0.0780773	synonymous-codon	MYCBP2	GRCh38.p7	13:77051091	TGTTGTTCCAAAACA[A/G]AAAAAAACAGCCACT	23077
rs201320617	snp	A/C	0.154661	0.231107	intron-variant	MYCBP2	GRCh38.p7	13:77223909	CACGAACTAAAACTA[A/C]AACTAAAACAAATGA	23077
rs201342476	snp	A/T	1.64841e-05	0.00287085	missense	MYCBP2	GRCh38.p7	13:77166457	TTCTGAACAGTTCTG[A/T]CAGGAATCAACAAAC	23077
rs201388190	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77166972	CAAAGACAAAACACA[C/T]ACATACACACACACA	23077
rs201408082	snp	A/G/T	0.000280542	0.0118404	missense	MYCBP2	GRCh38.p7	13:77098510	GCATTTTCTTCTTGC[A/G/T]GAGGGTATCTGGATC	23077
rs201417174	in-del	-/TTG	0.0271762	0.113356	intron-variant	MYCBP2	GRCh38.p7	13:77150621	GCAAATTTAATATCC[-/TTG]ATCAAATGCTCTTTG	23077
rs201437966	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77161399	AAAGCAAACAATAAT[-/A]AAAAACAACAAATGA	23077
rs201455771	in-del	-/AC	0.0479149	0.147179	intron-variant	MYCBP2	GRCh38.p7	13:77245873	CACACACATATATAT[-/AC]ACACACACACAAACA	23077
rs201462986	in-del	-/A	0.00755907	0.0610114	intron-variant	MYCBP2	GRCh38.p7	13:77144152	CACAGACACACCCAC[-/A]GGGGAGAGACAGGGT	23077
rs201464351	in-del	-/AA	0.154661	0.231107	intron-variant	MYCBP2	GRCh38.p7	13:77223914	ACTAAAACTAAAACT[-/AA]AACAAATGAAGTAGG	23077
rs201467354	snp	C/G/T	0.000225206	0.0106095	intron-variant	MYCBP2	GRCh38.p7	13:77164555	CCCTATGGAATTGCA[C/G/T]AAAATTTGCTGCTTT	23077
rs201476336	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77128834	TGAAAGTGTTGGCAG[A/C]AGAAAAAATAAAAGA	23077
rs201491157	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77072321	AAAAAAAAAAAAGAA[A/T]TCAAATGGGAATAAG	23077
rs201501710	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77199454	CTGCAAGGCGGCAGC[C/G]AGGCTGGGGGAGGGG	23077
rs201518602	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77071271	CACGTGTGTGCACAC[A/G]CACACACACACACAC	23077
rs201520245	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77177143	TTTCTTGAAAAATGA[A/C]AATATAAAAAAAAAA	23077
rs201556511	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77286787	AAAAAAAAAAAAAAA[A/T]AAATATATATATATA	23077
rs201562906	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77188390	AATGCTATGATGTAA[G/T]TTACTTAGGTAACAT	23077
rs201598847	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77118698	TTTTTTAATGGAAGC[A/G]CCCCACCAAATCTTA	23077
rs201603612	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77092081	GCATGTATTTTTAAT[A/G]AAAAAAAAAAAAAAC	23077
rs201604251	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77173321	AGCTTTCTGAAACAC[A/G]TAACTCTTACGCATA	23077
rs201618940	snp	A/G	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77157107	TTAATTTTTTTTTGA[A/G]ATAGGGTCTTGCTCT	23077
rs201627874	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77250239	AAAAAAAAAAAAAAA[A/T]CATATCTCAGCAGCC	23077
rs201663943	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77072318	AAAAAAAAAAAAAAA[A/G]AAATCAAATGGGAAT	23077
rs201674123	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77142952	ATTTCAGATAAAAGA[C/T]ACTCATCCCAAACCA	23077
rs201693569	in-del	-/ATT			intron-variant	MYCBP2	GRCh38.p7	13:77266696	TTTAATATTATTGTC[-/ATT]ATTATTATTATTATT	23077
rs201714806	snp	A/G	1.64836e-05	0.0028708	missense	MYCBP2	GRCh38.p7	13:77096362	ATTTTTCTCTACAGC[A/G]ATCACATACCAGATA	23077
rs201718297	in-del	-/G			intron-variant	MYCBP2	GRCh38.p7	13:77072318	AAAAAAAAAAAAAAA[-/G]AAATCAAATGGGAAT	23077
rs201721664	snp	A/C/G	5.60568e-05	0.00529394	synonymous-codon, missense	MYCBP2	GRCh38.p7	13:77055756	TTTTAGTACTATGTG[A/C/G]TTAATTTTGTTCTGC	23077
rs201733944	in-del	-/AA			intron-variant	MYCBP2	GRCh38.p7	13:77183782	CGAACTCCTGACCTC[-/AA]GTGATCCACCCACCT	23077
rs201739266	snp	A/C/G	8.24687e-05	0.00642093	synonymous-codon	MYCBP2	GRCh38.p7	13:77098904	CTGATCAGCAGTAGT[A/C/G]CGGCTCATACGTCCA	23077
rs201750287	snp	A/T			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77292530	GAAAGACACCAGATT[A/T]AAAAAAAAAAGAGCA	23077
rs201750399	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77157765	TCAAAAACAAACAAA[G/T]AAACAACCGCCAAAC	23077
rs201765075	in-del	-/T			intron-variant	MYCBP2	GRCh38.p7	13:77092666	CCTGACCTCAGGTGA[-/T]CCACCCGCCTTGGCC	23077
rs201767550	snp	C/G/T	0.000530353	0.016276	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087455	GTTTCTATAAAAATA[C/G/T]GCACAATCAAAACAA	23077
rs201768936	snp	A/G	0.00398564	0.0444627	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77077676	TACGATATGGCTTCC[A/G]AGCAAAATTATATGA	23077
rs201776748	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77169190	GAGGCGGGCGGATCA[C/T]GAGGTCAGGAGATCG	23077
rs201777858	in-del	-/AAAG			intron-variant	MYCBP2	GRCh38.p7	13:77055143	AGGTTAAAAAAAAAA[-/AAAG]AAGAAGTAGTTAAAG	23077
rs201784495	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77200100	AATTACTCTGAGCTA[C/T]GGGAGGACATTCAAA	23077
rs201785008	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77317141	ATTTGTAGTACAAAC[A/G]GGGTCTCACCATGTT	23077
rs201798735	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77174927	ATATATATTATATAT[A/T]TATAATATATATATA	23077
rs201826002	in-del	-/AAAC	0.0263992	0.111815	intron-variant	MYCBP2	GRCh38.p7	13:77318755	CGAGACTCTGCCTCA[-/AAAC]AAACAAACAAACAAA	23077
rs201835625	in-del	-/AT	0.0256215	0.110247	intron-variant	MYCBP2	GRCh38.p7	13:77275178	ATCCAGGGAAAGAAA[-/AT]AGTCAATAGTTTAAA	23077
rs201880594	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77259870	ACAAGTTTTTGAGAT[A/T]AGCATTTATAAATAT	23077
rs201896706	in-del	-/TG/TGTG			intron-variant	MYCBP2	GRCh38.p7	13:77071229	CCACATATGTATATA[-/TG/TGTG]TGTGTGTGTATATAT	23077
rs201898321	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77223914	ACTAAAACTAAAACT[A/C]AAACAAATGAAGTAG	23077
rs201916187	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77131525	ACAAACAAACACACA[A/C]ACACACACACACACA	23077
rs201924004	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77200989	ACTGCATCAATTAAC[A/G]AGCAAAATAACCAGC	23077
rs201959295	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77072316	AAAAAAAAAAAAAAA[A/G]AGAAATCAAATGGGA	23077
rs201968430	snp	C/T	3.31669e-05	0.00407215	missense	MYCBP2	GRCh38.p7	13:77169655	CTATGTAGGCTATAA[C/T]AAGGGGGAGCAGCAT	23077
rs201974403	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77286789	AAAAAAAAAAAAAAA[A/T]ATATATATATATATA	23077
rs201977083	snp	C/T	0.00199792	0.0315431	synonymous-codon	MYCBP2	GRCh38.p7	13:77164476	AAGTGCTAGGTCCTT[C/T]TTCATCAGAGCTGCT	23077
rs201978264	snp	G/T	0.000131933	0.00812089	missense	MYCBP2	GRCh38.p7	13:77051089	TGTGTTGTTCCAAAA[G/T]AGAAAAAAACAGCCA	23077
rs201986498	snp	C/T	0.00296356	0.0383796	intron-variant	MYCBP2	GRCh38.p7	13:77176458	TTAACTACATAATAA[C/T]ACCTCTTATTCACAA	23077
rs201990039	snp	C/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77198457	TTTAGATATTATTGA[C/G]AGAACTAAGAAAATA	23077
rs202007141	snp	A/G	0.00199805	0.0315442	intron-variant	MYCBP2	GRCh38.p7	13:77263606	TTAAGAGTATGAAAA[A/G]TTGAAAATTAAAATA	23077
rs202043205	snp	C/T	6.58892e-05	0.00573936	synonymous-codon	MYCBP2	GRCh38.p7	13:77067676	TCCTTTGGCTTTTAG[C/T]TGTACAGTGAGTGCT	23077
rs202055190	snp	A/G	0.000134467	0.00819851	intron-variant	MYCBP2	GRCh38.p7	13:77058196	GTCTGGATACATTCA[A/G]TACTTTAAAAGCTGA	23077
rs202064321	in-del	-/TAAAT	0.00676609	0.0577691	intron-variant	MYCBP2	GRCh38.p7	13:77206334	TTAACATAATATACA[-/TAAAT]TAAATATTATATACT	23077
rs202065288	snp	A/C/T	3.29527e-05	0.00405898	missense	MYCBP2	GRCh38.p7	13:77180252	TCCTGACTGGTAGCA[A/C/T]AACAATGACCAGCAT	23077
rs202082829	in-del	-/TGTGTG			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228692	CTAAGATGAATATGT[-/TGTGTG]TGTGTGTGTGTGTGT	23077
rs202088979	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77073344	AAAAGAATCCATTCT[A/G]ATAGAAATTCTCAGC	23077
rs202176824	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77222410	TTGTGTTTTTAATAA[G/T]AAGTTCAACTCAATG	23077
rs202176868	in-del	-/TA			intron-variant	MYCBP2	GRCh38.p7	13:77234012	GTACATATATATATA[-/TA]CATATATAAATACAT	23077
rs202206637	snp	A/G	9.91752e-05	0.00704115	synonymous-codon	MYCBP2	GRCh38.p7	13:77270382	CATCATTCTGAAGTA[A/G]ACATTGGTCATCTTC	23077
rs202233048	snp	A/G/T			intron-variant	MYCBP2	GRCh38.p7	13:77199407	CGCTCATGGAGTCTC[A/G/T]CTGATTGCTAGCACA	23077
rs202233238	snp	C/T	0.0129154	0.0793153	intron-variant	MYCBP2	GRCh38.p7	13:77144622	CAGTCAACATCATTA[C/T]GATAGTTCAGCAAAC	23077
rs202240362	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77111598	ATTTTTTTTTTTTTT[C/T]TTTTAAGTAGAGACA	23077
rs367545920	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77250037	GACCATCCCGGCTAA[A/C]ACGGTGAAACCCCGT	23077
rs367548125	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77299185	AAATCCAAATTCAGA[C/T]AGATTTCCTAAAGAC	23077
rs367548727	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77188261	GGGAAAGAAACATTC[C/T]TCCTATGCATTTTAC	23077
rs367551047	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77154924	TAAAAAATAAGATAG[A/C]GAAAGCATCAGAGTA	23077
rs367555175	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77289751	GTATTTTCTAAAAAA[G/T]AAATGTTTTTACTTG	23077
rs367559938	snp	C/G			upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77327501	AAACCATCCCAATTA[C/G]AAGTGCCTTTAGCGA	23077
rs367562338	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77263602	ATTTTTAAGAGTATG[A/G]AAAATTGAAAATTAA	23077
rs367571105	snp	A/C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77313868	AACAGACACCTCACC[A/C/G]AACAAGATATATAGA	23077
rs367581734	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77232348	GTTTTAAGTTGTGCT[A/G]GCTAAGGAAGAACAC	23077
rs367589616	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77142120	CTGAAATTTTACCAG[A/G]ATTTTTAGAGAAAAG	23077
rs367591474	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77200360	AAGAATAAAAAGAAA[C/T]GAACAAAGCCTCCAA	23077
rs367602410	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77153443	AGGGGTCAAGGGAAC[C/T]CTCCTGTCTCAAACA	23077
rs367604232	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77090768	TGGCTGCATCAAGGT[C/G]TCATGAGAGGTAACA	23077
rs367617985	snp	C/T	1.72779e-05	0.00293916	missense	MYCBP2	GRCh38.p7	13:77191808	AACATCATTGCATAT[C/T]TTTCTCTGAGAAAAA	23077
rs367631291	snp	C/T	0.000515756	0.0160503	intron-variant	MYCBP2	GRCh38.p7	13:77251112	TTGCAAAGAAATGTG[C/T]TCTGCACATGTTCTT	23077
rs367651238	snp	C/T	5.31835e-05	0.00515644	intron-variant	MYCBP2	GRCh38.p7	13:77097346	AAAAAAGCACTTATA[C/T]GTACATTCAACAGTA	23077
rs367656843	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77050588	GCTCACTACACTACT[A/G]ATTCCCAGCCATTCT	23077
rs367663098	snp	G/T	1.64974e-05	0.00287201	missense, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076789	CAGGTGATGACAATA[G/T]TGCTTTTTCCTCTTG	23077
rs367666253	snp	C/T	3.36615e-05	0.00410239	synonymous-codon, nc-transcript-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087556	CACTGGTGCAGGAGT[C/T]AGTGATGCCACAAAA	23077
rs367673507	snp	C/T			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076192	AAAATTTACTAAACA[C/T]GTGTGTGATGCTACC	23077
rs367687841	snp	G/T	1.93283e-05	0.00310866	missense	MYCBP2	GRCh38.p7	13:77055762	TACTATGTGATTAAT[G/T]TTGTTCTGCAATAAA	23077
rs367691739	in-del	-/G			intron-variant	MYCBP2	GRCh38.p7	13:77311579	TGTTTTTTTTTTTTT[-/G]TTTTTTTTTTAAAGA	23077
rs367726903	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77217197	AAATGTCATCTCAGA[C/T]ACTTAGGTTCAAGAG	23077
rs367728959	in-del	-/AT	0.00636936	0.0560724	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77080656	AGTAGACACTTGAAG[-/AT]ATAGGCTGGGTGCAG	23077
rs367752994	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77046982	CAACATATCAATGGT[A/G]GTGACACAAACTGCA	23077
rs367784750	snp	A/G	3.51278e-05	0.00419078	intron-variant	MYCBP2	GRCh38.p7	13:77045545	TTTAAGAATACACAC[A/G]TATAAACCTCACAGA	23077
rs367816837	snp	A/C	0.000153988	0.00877328	intron-variant	MYCBP2	GRCh38.p7	13:77093381	GATGGCAATACAGAT[A/C]CTCTCCATTTTTAAT	23077
rs367828120	snp	A/C	0.000167972	0.00916284	missense, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326506	AGCGCTGCCGCCCCC[A/C]TGGTCCCTGTCATTG	23077
rs367834587	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77174899	AGAATATTAGCCATA[C/T]TATATATATATAATA	23077
rs367864042	snp	C/T	0.000153988	0.00877328	intron-variant	MYCBP2	GRCh38.p7	13:77261404	AAAAAAAAGGAATTA[C/T]GGTACTTTTTGGAAT	23077
rs367871922	snp	A/G	0.00277923	0.0371738	intron-variant	MYCBP2	GRCh38.p7	13:77166314	CACATAAAACAGAAG[A/G]AAAAAAAAACTTACC	23077
rs367875741	snp	A/C	3.34113e-05	0.00408712	intron-variant	MYCBP2	GRCh38.p7	13:77251135	ATGTTCTTTAGTAGG[A/C]ATCATTGTCTCTTAC	23077
rs367885877	snp	C/T	0.000247095	0.0111124	missense	MYCBP2	GRCh38.p7	13:77144507	GCCCCTGGAGTCCAA[C/T]TTGCACAATAAGTCC	23077
rs367886310	snp	A/G	4.97533e-05	0.0049874	intron-variant	MYCBP2	GRCh38.p7	13:77205402	GAATATATAAATCAT[A/G]ATCTATGTTTTAAAA	23077
rs367907213	snp	A/T	0.000218408	0.0104478	intron-variant	MYCBP2	GRCh38.p7	13:77057135	AAGCAAATATAATAA[A/T]GATAAACAGTTGAGT	23077
rs367910147	in-del	-/TAAAT			intron-variant	MYCBP2	GRCh38.p7	13:77144289	TGTTAATGCACTAAT[-/TAAAT]ACTCATTATGAAAGA	23077
rs367928347	snp	C/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77287709	GGCTTTGTAGTTCTA[C/T]TTCAAGAAAAATAAA	23077
rs367936445	snp	C/T	0.000199853	0.00999434	intron-variant	MYCBP2	GRCh38.p7	13:77288116	ATTATAGCCAGAACA[C/T]CTGCAGGTTACACAT	23077
rs367938429	snp	C/T	0.000153988	0.00877328	synonymous-codon	MYCBP2	GRCh38.p7	13:77176557	GGGTGAGTCATCCGT[C/T]GTGTACGTTCCTTTC	23077
rs367957407	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77093577	TTTTGAGAACTTTTC[C/T]ATCTTCCAGTGTTTT	23077
rs367974168	snp	A/C/T	0.00875692	0.0656968	intron-variant	MYCBP2	GRCh38.p7	13:77210393	GAGACAGGGTTTCAC[A/C/T]GTGTTAGCCAGGATG	23077
rs367975301	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77186719	TTAAATGACAACAGA[C/T]ACCACCTGAATCTCA	23077
rs367979579	snp	A/G	0.00021435	0.0103503	synonymous-codon	MYCBP2	GRCh38.p7	13:77261256	GGCGTGAGAGCCATC[A/G]TGTCCAACTGAGAAG	23077
rs367987070	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77315300	ATGTAACTCACTTTA[C/T]GAGACGAGGATAACT	23077
rs367989717	snp	A/G	1.91287e-05	0.00309257	intron-variant	MYCBP2	GRCh38.p7	13:77051953	AGATTACAGCAGGAA[A/G]AAAGAAAACTCTGGC	23077
rs367995669	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77125271	AACAAAAGCAATACA[A/G]TAGGCATTAAACTTC	23077
rs368010045	snp	A/T	1.65326e-05	0.00287507	missense	MYCBP2	GRCh38.p7	13:77098074	CTGGCACATTCGGCC[A/T]CAGAAGGAGACATGG	23077
rs368037205	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77200522	GCAGGCCAACATTCA[A/G]ATTCAGGAAATACAG	23077
rs368061872	snp	A/G	1.6571e-05	0.0028784	missense	MYCBP2	GRCh38.p7	13:77097955	AACTACTCCTTATAG[A/G]AGCATGTTCTTTGGA	23077
rs368081404	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77106205	AGTAGCATATATTAT[C/T]TTTGAGTGTTGAGTC	23077
rs368103288	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77202139	CAAAATTGATAGACC[G/T]CTAACAAGACTAATA	23077
rs368104139	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77175563	TTATCCAAAATTCTG[A/C]TCTATAATGAAATTT	23077
rs368107169	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77282589	TGTTCTTGATCCCAC[A/C]CCCTCCGATCTCTCA	23077
rs368118401	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77173331	AACACGTAACTCTTA[C/T]GCATAACAGAGTTTT	23077
rs368141542	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77109550	ATATTGTTAATTACC[A/G]GCCTGGCAAAAGTTC	23077
rs368148302	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77304191	CCATGTTCACTGCTA[C/T]ACTATTCACAATAGC	23077
rs368169983	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77159287	AATGCATATAAAGTA[C/T]ATAATACATTGCCTA	23077
rs368205678	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77183936	GGAGTTTACCAACTT[C/T]TTTTCTTCAAAAAAC	23077
rs368205988	snp	A/G	0.000307953	0.0124049	synonymous-codon	MYCBP2	GRCh38.p7	13:77156181	TTTCTGAGGATCCGC[A/G]TATGAATCTGGCTGA	23077
rs368206108	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77134407	GGTGTGGTGGTGTAT[A/G]CCTGTAATACCAGCT	23077
rs368206459	in-del	A/CC			intron-variant	MYCBP2	GRCh38.p7	13:77301863	ATTTATAAAAAAAGA[A/CC]CCAAGTGGACATTCT	23077
rs368208189	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77047487	AATTTATATACTGAC[A/G]TGTTAATGAAAGGAG	23077
rs368209761	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77133733	ATTAGTTCACATACA[C/T]AGCATGTCCCCATAA	23077
rs368225135	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77320300	CCTGAAAGCGGGATC[C/T]GAAAGCCTAACCACA	23077
rs368228999	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77305132	TAGACTCTTTTAGAC[A/G]ATATAAAAAGAAGAA	23077
rs368229385	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77202933	ACAAACCCACAGCCA[A/G]TATCATACTGAATGG	23077
rs368235641	snp	C/T	8.26003e-05	0.00642599	synonymous-codon	MYCBP2	GRCh38.p7	13:77211280	ATTTATCAGAAGGCA[C/T]TTAAATGGAGGAGGT	23077
rs368238213	snp	C/T	4.95307e-05	0.00497623	missense	MYCBP2	GRCh38.p7	13:77098327	CTGTTAGACTATTTG[C/T]TTTTAAAGTACTTGA	23077
rs368239193	snp	A/C	1.64781e-05	0.00287033	missense	MYCBP2	GRCh38.p7	13:77157945	CATTTACCTTGCAAG[A/C]CTTCCACCACTTGAT	23077
rs368244954	snp	A/C			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77084059	GAATAAAAATACCAT[A/C]GTTTATTTCATCAGT	23077
rs368245125	snp	A/T	0.000153988	0.00877328	synonymous-codon, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081532	TTTATCTTCATCTCC[A/T]GATTCCCAAAAGGTT	23077
rs368279791	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77095189	AAATACCTATTACCA[C/T]AAAGTCATTATGTCA	23077
rs368288211	snp	C/T	3.37598e-05	0.00410838	intron-variant	MYCBP2	GRCh38.p7	13:77140192	AGATAAACAGTGAGG[C/T]AGGAAGAACATAGAA	23077
rs368294060	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77114186	ATTACATTGCAAAAA[C/T]AGACCCAAAAGGAAC	23077
rs368299928	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77066842	GTTTACTGGCATTTA[C/T]AAGTTTTTTTCTGTG	23077
rs368301696	snp	A/C/G	0.000153988	0.00877328	missense, synonymous-codon	MYCBP2	GRCh38.p7	13:77185219	GAAGGACAGCTTCTA[A/C/G]AAGACTCAAGGGTTG	23077
rs368306266	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77189313	ATATATAATGTATAT[A/G]ACATATAACTTATAT	23077
rs368323389	snp	C/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77050883	AATTCCTCCTGCTTC[C/T]TTAGGCTAGTTTGAA	23077
rs368325414	snp	C/T	3.44851e-05	0.00415227	intron-variant	MYCBP2	GRCh38.p7	13:77126272	TTTGGTTGTATTACA[C/T]TAAAAATGAGTATCT	23077
rs368337423	snp	C/T	1.64757e-05	0.00287012	missense	MYCBP2	GRCh38.p7	13:77059579	ACTCTGTTCCACTCC[C/T]GGAACCACAGAAGCG	23077
rs368379465	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77146065	AAATGCTATAAAGTA[A/T]TTATTTATAGAAAAT	23077
rs368384737	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77070409	AGTATTAGGAGATTT[C/T]TTTTTCTTGCAATTT	23077
rs368399415	snp	A/G	3.44021e-05	0.00414727	intron-variant	MYCBP2	GRCh38.p7	13:77095311	TATCAATAAACAATC[A/G]CTGTTAATCCAAAGG	23077
rs368438330	snp	A/G	0.000153988	0.00877328	intron-variant	MYCBP2	GRCh38.p7	13:77191842	AGTGAGTCAAAAACA[A/G]TATTTTCTTACTTCT	23077
rs368474102	snp	C/G/T			intron-variant	MYCBP2	GRCh38.p7	13:77128503	AACTAATTATAATTG[C/G/T]AAACTAGTCACTGAA	23077
rs368491573	snp	A/T			intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075056	TCTGCAGATATATTA[A/T]AATCAGCTGGGCACG	23077
rs368501535	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77114517	ATAGTACTTTAGTGT[A/G]TTCATATTCTCAAAT	23077
rs368502518	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77203405	AAAAGAGGATACAAA[C/G]AAATGGAAGAACATC	23077
rs368507698	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77236009	GAATAGCCTTTTGGT[C/T]TTAAACAGAGAAGTG	23077
rs368509244	snp	A/T	2.08723e-05	0.00323043	intron-variant	MYCBP2	GRCh38.p7	13:77186108	AATTAATTCAAATGA[A/T]ACCATAAACGGAATC	23077
rs368527680	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77305300	CCCAAATGCTCACCA[A/G]CTAATGAATGTATAA	23077
rs368539114	snp	A/G	0.000153988	0.00877328	intron-variant	MYCBP2	GRCh38.p7	13:77151000	TATTTAATTGTCACT[A/G]ACATCAAAATAAGCA	23077
rs368544796	snp	A/G	3.34499e-05	0.00408948	synonymous-codon	MYCBP2	GRCh38.p7	13:77061296	TTCTTCTTCTTCTTT[A/G]AAGACCTATTATTTC	23077
rs368552600	snp	A/C	0.000153988	0.00877328	missense	MYCBP2	GRCh38.p7	13:77171549	GAACGACAGTGCTTA[A/C]AACAGACAATGCTCT	23077
rs368563196	in-del	-/TT			intron-variant	MYCBP2	GRCh38.p7	13:77174919	TATATATAATATATA[-/TT]ATATATATATAATAT	23077
rs368569293	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77312691	GAGGAAGAAAGGAAC[A/T]AAAAAAGAGAAACAG	23077
rs368581011	snp	A/C	0.000153988	0.00877328	intron-variant	MYCBP2	GRCh38.p7	13:77263646	CACTTAATTTGCTAT[A/C]TTACTTATAATATGC	23077
rs368617424	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77191043	AATGTTGGATTTAGA[A/G]TCAACAGGTTACAGG	23077
rs368619287	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77289362	CAATATATAAAAAAG[C/T]AATACATTATGACCA	23077
rs368626955	snp	C/T			missense	MYCBP2	GRCh38.p7	13:77262127	CCTCATCAAATCCTG[C/T]ACCTGAAATACGAGA	23077
rs368641011	snp	C/G	3.31719e-05	0.00407245	missense	MYCBP2	GRCh38.p7	13:77205476	AAGTATACATACTTT[C/G]AAACCTGTTTACCAC	23077
rs368647528	snp	C/G	0.000153156	0.00874955	intron-variant	MYCBP2	GRCh38.p7	13:77096520	TATTTAACACTCCAA[C/G]TGTCCTTAATAGTTT	23077
rs368647771	snp	C/G	1.65165e-05	0.00287367	synonymous-codon, utr-variant-5-prime	MYCBP2	GRCh38.p7	13:77288179	TGGAAGCTTGATAGG[C/G]GGCTCTTTGGATTCC	23077
rs368651865	snp	C/G	1.66588e-05	0.00288602	intron-variant	MYCBP2	GRCh38.p7	13:77068848	TATTTAAAGTTAACA[C/G]AGAACATGTAAAAAT	23077
rs368660041	snp	A/C/T	0.000150522	0.00867409	intron-variant	MYCBP2	GRCh38.p7	13:77088797	ACATGATTTGTATAA[A/C/T]CAATGAATCAGTAAT	23077
rs368678020	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77201135	CCATCAGTGTGCTGT[A/G]TTCAGGAAACCCATC	23077
rs368691722	snp	A/C	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77252195	GGATTCCTTCACGGC[A/C]AGAAATCAGCAAACC	23077
rs368699605	in-del	-/GTCTGAATGAACT	0.0189856	0.0955633	intron-variant	MYCBP2	GRCh38.p7	13:77190694	GCCATGACATTCCAA[-/GTCTGAATGAACT]GTCTATGAAAATCAT	23077
rs368710108	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77174893	ACTGCTAGAATATTA[G/T]CCATACTATATATAT	23077
rs368713277	in-del	-/C	0.0236746	0.106192	intron-variant	MYCBP2	GRCh38.p7	13:77301416	CTACAGAGCAAGACT[-/C]CATCTCAAAAAAAAA	23077
rs368720361	snp	C/T	3.68439e-05	0.00429192	intron-variant	MYCBP2	GRCh38.p7	13:77212190	AAACCATATTAGCAA[C/T]ATTGCTGTGTAAACA	23077
rs368723070	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77272019	TGGCAGGTCTGTAGA[A/G]AACTGCAGCTATTGA	23077
rs368726492	snp	C/G/T	0.000153988	0.00877328	missense, intron-variant	MYCBP2	GRCh38.p7	13:77126527	TGAAAAAGTCATCAG[C/G/T]ATTAGTTTTAGATTC	23077
rs368726958	snp	A/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77155194	TAAGCAATGTGTTCT[A/T]ATTTTTTACTTAGGT	23077
rs368731630	in-del	-/TATTTT			intron-variant	MYCBP2	GRCh38.p7	13:77270871	TCGATCCATGTTTCT[-/TATTTT]ATCTTCCATATTTCT	23077
rs368737966	snp	C/T	4.96323e-05	0.00498133	intron-variant	MYCBP2	GRCh38.p7	13:77157901	GAAGAAAGATGAAAG[C/T]CCTAAAATAAAGTAA	23077
rs368739801	snp	C/T	0.000153988	0.00877328	missense	MYCBP2	GRCh38.p7	13:77055719	CATCCTCATAGAGTT[C/T]TTTTATTGGATCAAG	23077
rs368741681	snp	A/G	0.000153988	0.00877327	intron-variant	MYCBP2	GRCh38.p7	13:77089043	ACTTCTATTAAAGAA[A/G]AAGAAAATTATTAAT	23077
rs368779649	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77103976	AAAAAATGTTAGGAA[C/T]GTCAATGATTTACTA	23077
rs368800349	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77048644	CTCCCTAGCCCTCAA[A/T]TTTCCATTTGATAAC	23077
rs368803460	in-del	-/GTGAA			intron-variant	MYCBP2	GRCh38.p7	13:77059119	CCACATTCTTATTAA[-/GTGAA]TTGAGAAACCAAAAA	23077
rs368825757	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77099495	AACTGAATTTATGCA[C/T]AGACACAATTATAAT	23077
rs368829213	snp	C/T	0.00597247	0.0543191	intron-variant	MYCBP2	GRCh38.p7	13:77050648	AACGGTTCCAGGCTT[C/T]GTTAAAAAAAAAAAA	23077
rs368842824	snp	C/T	7.2808e-05	0.00603313	intron-variant	MYCBP2	GRCh38.p7	13:77243779	GAGGACAACTCAGTG[C/T]AGCATAGTATAATCA	23077
rs368846600	snp	C/T	4.94629e-05	0.00497283	missense	MYCBP2	GRCh38.p7	13:77058355	CGTTTTTAACACCCC[C/T]GCATGGATGGCCACA	23077
rs368877996	snp	A/T	6.59914e-05	0.00574381	synonymous-codon	MYCBP2	GRCh38.p7	13:77177925	GTTAGCACTAGCTTT[A/T]ACAGAGTGAAGAGAA	23077
rs368880586	snp	C/T	1.65037e-05	0.00287256	synonymous-codon	MYCBP2	GRCh38.p7	13:77061197	GAATTCCACCATTGC[C/T]TTCATTGTTTTAGAA	23077
rs368923189	snp	C/T	8.60163e-05	0.0065575	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77078794	TTTCTCTCTAGGTAG[C/T]GAAACATTTAATGAC	23077
rs368924227	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77089685	ATTAAGGGCTATTTA[A/T]ATCCCCAAAGTTTTA	23077
rs368931889	snp	A/G			synonymous-codon	MYCBP2	GRCh38.p7	13:77251225	GTCTCCACAGACAGT[A/G]CAAACCATGCACTGC	23077
rs368972148	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77114710	TATCATATATTTCAT[A/G]TTTGAAATTGCTGGA	23077
rs369007025	snp	A/T	2.05916e-05	0.00320864	intron-variant	MYCBP2	GRCh38.p7	13:77267981	AAATATTTATTACTA[A/T]TTCAGCAGAAACAGC	23077
rs369018459	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77056761	AAATGAACTTTCTCA[C/T]GTAATATGTTTAACA	23077
rs369042984	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77052348	GGATCATAGGTGCAC[A/G]CCACCACACCCGGCT	23077
rs369058514	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77107016	ACATACCTACGTTTA[A/T]GTATTTATATATATT	23077
rs369059812	snp	C/T	3.50036e-05	0.00418337	intron-variant	MYCBP2	GRCh38.p7	13:77206611	AAACCCTGGACAGCA[C/T]ACATTAATGTGAATT	23077
rs369071454	snp	C/T	6.60742e-05	0.00574741	intron-variant	MYCBP2	GRCh38.p7	13:77168418	AATCACACTAAGAAC[C/T]GGTGCCTACCTTGTA	23077
rs369092962	snp	C/T	8.35122e-05	0.00646136	intron-variant	MYCBP2	GRCh38.p7	13:77169596	AAACATTCAAAGTTA[C/T]AGAATTAAATTACAC	23077
rs369109891	snp	A/C/G	9.91038e-05	0.00703869	missense	MYCBP2	GRCh38.p7	13:77088965	TATTAATTTTCATA[A/C/G]	23077
rs369111856	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77268306	CTATTTGAAAATGAA[C/T]AGCATAGTGGTTTCA	23077
rs369112050	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77315498	TTTAACATTCAAAAA[C/T]TAATTAATGTAATTC	23077
rs369112343	snp	C/G	5.44618e-05	0.00521804	intron-variant	MYCBP2	GRCh38.p7	13:77058452	GTATGTAAAAAAGCA[C/G]ACATTCTGGTAATTT	23077
rs369127845	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77319709	AGGAATAGCATTCCA[A/G]CTCACCACCAGTGAA	23077
rs369180688	in-del	-/ATT			intron-variant	MYCBP2	GRCh38.p7	13:77072993	TTTAAAAACATCTTT[-/ATT]GAGATATAGTTCACA	23077
rs369181084	snp	C/T	1.66382e-05	0.00288424	missense	MYCBP2	GRCh38.p7	13:77097460	TCTCTGGTCCTCCTA[C/T]TGCCAGCTGGGCCAT	23077
rs369183826	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77135689	TCACCACCCAAAACA[G/T]AAATCCTTATGTCAT	23077
rs369184643	snp	A/G	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77213707	ACATTTAAATTCATA[A/G]AAGTTCACAACTAGG	23077
rs369203327	snp	C/T	4.95438e-05	0.00497689	missense	MYCBP2	GRCh38.p7	13:77166389	ATTTCTTTAATTCTA[C/T]CCATGAATTAAGATT	23077
rs369214006	in-del	-/G			intron-variant	MYCBP2	GRCh38.p7	13:77072300	CATTTCAAAAAAAAA[-/G]AAAAAAAAAAAAAAA	23077
rs369230161	snp	A/G	0.00795532	0.062565	intron-variant	MYCBP2	GRCh38.p7	13:77240437	ACATGGTGAAACCTC[A/G]CCTCTACTAAAAATA	23077
rs369258451	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77199951	TGGGGAAAAAACAGA[A/G]CAGAAAAACTGGAAA	23077
rs369260935	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77155745	ATTCTTTCATGCATT[C/T]ATTCAATCAATACAT	23077
rs369273195	snp	C/T			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291842	TTAACGCTGCAGGCA[C/T]GATTGCTTACTCCTT	23077
rs369277478	in-del	-/CTG			intron-variant	MYCBP2	GRCh38.p7	13:77253619	GGGCTTTCTGGGCTG[-/CTG]GTAATATGTGGTTTC	23077
rs369278773	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77296977	GTGTTTTATACTTTA[A/T]CCATAGTGGGATGTT	23077
rs369278934	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77274286	TGAAGATGAAACACA[C/T]ACACACACAAATGTT	23077
rs369279158	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77156847	GCATTACATAAAAAC[A/G]TCTGCATAGTATAGT	23077
rs369333299	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77286450	TAACTATATCTACTA[C/T]ATAGAAAAAATATAT	23077
rs369345138	snp	A/G	0.00109516	0.0233748	intron-variant	MYCBP2	GRCh38.p7	13:77224400	AAAAGAAGGAAAAGA[A/G]AACAGAAGAAAAAAT	23077
rs369353648	snp	G/T	3.33656e-05	0.00408432	intron-variant	MYCBP2	GRCh38.p7	13:77174284	ACCACTGTAAAGTAT[G/T]TCCGTTATCTCTATA	23077
rs369359736	snp	A/T			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77085473	CTGTGTACTTTCTGA[A/T]TCTTTTTCTCTGCCT	23077
rs369361199	snp	C/T	0.000133469	0.00816803	intron-variant	MYCBP2	GRCh38.p7	13:77139164	CAAACAGCGTGTATC[C/T]ATAATGCTTTTTAAA	23077
rs369371747	snp	C/G	1.65222e-05	0.00287417	missense	MYCBP2	GRCh38.p7	13:77095512	GGGACAGCAGGAAGA[C/G]TGCATTGGCTTTAAT	23077
rs369373750	snp	A/G	4.99763e-05	0.00499856	intron-variant	MYCBP2	GRCh38.p7	13:77061811	ATAAGACATTTCCAC[A/G]TTACTTAGATTAACA	23077
rs369377951	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77061014	ATGCTCTCTTCACCA[C/T]AGAACACTCTATATA	23077
rs369379958	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77314128	AAACCTACTCTTAGC[A/C]CGTGATCCCACAATC	23077
rs369381169	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77247217	GAAAACCCTAAAGAT[G/T]GCACTCAAAAAAACC	23077
rs369384332	snp	A/C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77272440	ATTCATAAGCTCATA[A/C/T]GTTGGTGGTCACTAT	23077
rs369389626	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77190527	ATGAAAGAACTGAAC[A/G]TGATTAGGACTCCTA	23077
rs369397476	snp	C/T	0.00132564	0.0257111	intron-variant	MYCBP2	GRCh38.p7	13:77267948	TAACCCTGATAACAG[C/T]AAAAAATTTTCCTGT	23077
rs369419146	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77131345	AAGACAGAGAGACCT[C/T]GTCTCTACAAAATAA	23077
rs369423674	snp	C/G			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77082525	GTGAGTCCAGTATGT[C/G]AATCTAGTAACAAGG	23077
rs369428371	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77193839	AATAACTGTATTATT[A/G]CTAGAACACCAGCAA	23077
rs369435483	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77138121	CTTATAGATGTATCA[C/T]TGTTCAACTTAACCT	23077
rs369443685	snp	C/T			synonymous-codon	MYCBP2	GRCh38.p7	13:77243864	AATTCCTCTTTGTCT[C/T]GCCTCTTGACCATCT	23077
rs369448891	in-del	-/AC			intron-variant	MYCBP2	GRCh38.p7	13:77131487	AAGACTTCATCTCAA[-/AC]ACACACACACACACA	23077
rs369449185	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77112822	TCTTTCAACTGAATT[A/C]CTCTCATTAGAAAAC	23077
rs369454450	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77174948	TATATATATATTTTA[A/T]ATATTATATATATAT	23077
rs369460802	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77259214	AGGTTGCAGTAAGCT[G/T]AGATTGTGCCACTGC	23077
rs369461038	in-del	-/AACATAACAT			intron-variant	MYCBP2	GRCh38.p7	13:77317939	AAGACTCCGTCTCAA[-/AACATAACAT]AACATAACATAACAT	23077
rs369470663	snp	C/T	1.6557e-05	0.00287719	missense, intron-variant	MYCBP2	GRCh38.p7	13:77126476	TATCTTGTTCTTGCA[C/T]TGTTGCTTCCTGTGG	23077
rs369495855	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77069875	TCCCTCTCGAAAAAA[A/G]AAAAAGTTAGAATAA	23077
rs369499367	in-del	-/T			intron-variant	MYCBP2	GRCh38.p7	13:77059075	ATTTTTTTTTTTTTT[-/T]AAAAAGGTACCTTTG	23077
rs369532282	snp	C/G	6.61081e-05	0.00574888	intron-variant	MYCBP2	GRCh38.p7	13:77064769	ATTTTAATAAGTGAC[C/G]AGAAATGTATTACCA	23077
rs369553141	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77275011	TTGGAGGAAGGATGG[A/G]TAGATGGAAATATGG	23077
rs369553651	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77203483	GCCCAAGGTAATTTA[C/T]AGATTCAATGCCATC	23077
rs369562463	snp	C/T	0.000153988	0.00877328	intron-variant	MYCBP2	GRCh38.p7	13:77189062	TCTAAAGGCAGTAGA[C/T]ACATATAAAATTATG	23077
rs369585749	snp	C/G/T	0.000247427	0.01112	synonymous-codon	MYCBP2	GRCh38.p7	13:77098748	GCTAGAAGGCATCCT[C/G/T]CCATCAGATTTCAAT	23077
rs369591612	snp	A/C	0.000247793	0.0111281	intron-variant	MYCBP2	GRCh38.p7	13:77225415	AAAACGCAGTTATAC[A/C]CTAAAGTTCCAGCCG	23077
rs369600531	snp	A/G	4.94523e-05	0.00497229	synonymous-codon	MYCBP2	GRCh38.p7	13:77051085	AAAATGTGTTGTTCC[A/G]AAACAGAAAAAAACA	23077
rs369634987	in-del	-/AAGT			intron-variant	MYCBP2	GRCh38.p7	13:77244705	CTGCACAGCAAAAGA[-/AAGT]ATCATCAGAGTGAAC	23077
rs369662313	snp	C/T			missense	MYCBP2	GRCh38.p7	13:77097634	AAGCAGCTTTGATAG[C/T]AGCCAAAGAGATGTC	23077
rs369668756	snp	A/G	4.94482e-05	0.00497209	synonymous-codon	MYCBP2	GRCh38.p7	13:77139312	CATCATTCAGCCTCA[A/G]CCACACACCATCATC	23077
rs369704783	snp	A/C/T	0.000116235	0.00762274	intron-variant	MYCBP2	GRCh38.p7	13:77095607	GATTGTTTGACCTGG[A/C/T]GAAGAAAAAAATCAA	23077
rs369713320	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77047849	TGCGGGCCAAGACAG[C/T]CCACAGACTAAGCAC	23077
rs369723309	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77283294	TCTCTCTCTTGCTCT[A/G]TCTCAGCCAGTGTTG	23077
rs369755823	in-del	-/GAC			intron-variant	MYCBP2	GRCh38.p7	13:77063582	AAAAAAAAAAAAAAA[-/GAC]AACTGTTTTCAGAAA	23077
rs369757801	snp	A/G	3.30972e-05	0.00406786	missense	MYCBP2	GRCh38.p7	13:77260581	AAGGTTTGGATTGCC[A/G]TCTGCTCTTAGCTTT	23077
rs369775974	snp	C/T	1.65012e-05	0.00287234	missense	MYCBP2	GRCh38.p7	13:77161919	ACCTGCAATGCAGCC[C/T]CCTCAAGAATTTCAA	23077
rs369779556	snp	C/T	0.000153988	0.00877328	missense	MYCBP2	GRCh38.p7	13:77186041	CTCCAGTGAAGAATA[C/T]TCAACAATGACTCAA	23077
rs369779701	snp	C/T	1.64776e-05	0.00287028	missense	MYCBP2	GRCh38.p7	13:77066039	TCTCTGAGATCTGGG[C/T]AGGGGTTGAGCCCTT	23077
rs369790644	snp	C/T	0.000153988	0.00877328	missense	MYCBP2	GRCh38.p7	13:77098566	CGTTCCCGAGGAGGA[C/T]CAAGCTTTGTCTTAA	23077
rs369810319	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77061490	AGAAATTAAGTGTTT[C/T]TAAGGATAAAACAAC	23077
rs369825218	snp	C/T	0.000115899	0.00761157	missense	MYCBP2	GRCh38.p7	13:77270057	ATGTAGAATTGTATA[C/T]ATGGCCCTGCAAAAA	23077
rs369831910	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77149077	TAACTCTATCTCTAT[C/T]AATAAGACCCCATAC	23077
rs369840419	snp	A/G	0.00914312	0.0669923	intron-variant	MYCBP2	GRCh38.p7	13:77296152	AGGCTGGGCACAGTG[A/G]CTCATGTCTGCAATG	23077
rs369884004	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77241493	AGATAGAATGGTAAC[G/T]AATCTGAAAAAATTA	23077
rs369885556	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77248428	TCAACAACAACAAAA[G/T]AAACTGACAACCTGA	23077
rs369893551	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77199578	CTCTGTAGGCTCCAC[C/T]TCTGGGGGCAGGGCA	23077
rs369943113	snp	G/T	1.65323e-05	0.00287505	missense	MYCBP2	GRCh38.p7	13:77206757	GACTGCATGTCTGCT[G/T]CAGAGGGAAGCCTGG	23077
rs369948518	snp	C/T	1.65726e-05	0.00287855	intron-variant	MYCBP2	GRCh38.p7	13:77225599	TTAAGCCATTATTCA[C/T]CTTCAAAATAAAAAT	23077
rs369963541	snp	C/T	5.0929e-05	0.00504598	intron-variant	MYCBP2	GRCh38.p7	13:77140203	GAGGTAGGAAGAACA[C/T]AGAATAGAGATCTTA	23077
rs369984255	snp	C/G/T	6.81064e-05	0.00583517	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081811	TAACTAACAGGACAA[C/G/T]CAGGATAATAACTGA	23077
rs369986996	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075678	TGATTTCTTTTTGGG[A/G]GGGGTGAGGGGAATG	23077
rs370002127	snp	C/T	0.00039555	0.0140577	synonymous-codon	MYCBP2	GRCh38.p7	13:77257744	ACCAAATGTCCACAC[C/T]TCTCCATTCTTCATT	23077
rs370010038	snp	A/G	1.65792e-05	0.00287912	missense	MYCBP2	GRCh38.p7	13:77169642	GCAGCTACTGGTCCT[A/G]TGTAGGCTATAATAA	23077
rs370017897	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77181131	TCCAACCCCTACCGG[C/T]AGAAAAATTTCAAGA	23077
rs370018704	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77201845	GTTCTTTGAAACCAA[C/T]GAGAACAAAGACGCA	23077
rs370021830	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77154797	TTTCATATCACTATC[A/T]GGATAACTTTATTTT	23077
rs370030949	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77273802	CTTTGCTTTAGTTTC[C/T]TTCTAGTTACTCTCT	23077
rs370036386	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77129657	ATGCAATTATCATTA[C/T]GAATAATAATGGCAT	23077
rs370039299	in-del	-/TTTGTTTTTTTTTT			intron-variant	MYCBP2	GRCh38.p7	13:77311576	TTTTGTTTTTTTTTT[-/TTTGTTTTTTTTTT]AAAGAACCAAATGTA	23077
rs370071486	snp	A/G	4.94907e-05	0.00497422	intron-variant	MYCBP2	GRCh38.p7	13:77144575	TCTGAAAAGAAATAA[A/G]ATGGATATTGGAAAT	23077
rs370096422	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77106780	AGGTTCAAGGGGGAC[A/G]TGTGTAGGTTTGTTA	23077
rs370096587	snp	A/G	8.30613e-05	0.00644389	intron-variant, nc-transcript-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076896	ATGACAGGCATTAAC[A/G]CTATATTGGCCAGAG	23077
rs370098506	snp	A/G	6.59131e-05	0.0057404	synonymous-codon	MYCBP2	GRCh38.p7	13:77243156	AACCCCGGGCACTGG[A/G]ACAGCTAGATGATTG	23077
rs370118596	snp	G/T	3.62312e-05	0.00425609	intron-variant	MYCBP2	GRCh38.p7	13:77273683	TCTGTGGATAAAATA[G/T]AATTCAATTATATTC	23077
rs370137023	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77170141	CTTAGGTTCACAACA[A/G]TATTCCTCTCATTTG	23077
rs370165348	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77065355	TCCTCCCACTTCTCA[C/T]ATCCACATGATTTAA	23077
rs370165805	snp	A/G	1.70179e-05	0.00291696	intron-variant	MYCBP2	GRCh38.p7	13:77070744	AAAAAAAAAAAAAGA[A/G]TGAAGTGGTCTCTTT	23077
rs370173382	snp	C/T	3.29734e-05	0.00406025	missense	MYCBP2	GRCh38.p7	13:77261309	TAATTGGTAGCTCAA[C/T]CCATTTTCCTGCTGA	23077
rs370179285	snp	A/C	5.06385e-05	0.00503157	intron-variant	MYCBP2	GRCh38.p7	13:77156009	AAAATTTTATCAGTC[A/C]TTGCAGCCAGTATAT	23077
rs370182215	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77120383	AATACTTTGTGGAAA[A/G]TAATGAAGCTATTCA	23077
rs370183337	snp	G/T	1.68675e-05	0.00290405	intron-variant	MYCBP2	GRCh38.p7	13:77181681	TGCCTCTGTATAAAA[G/T]ATTTCAGAGACAGAC	23077
rs370187475	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77093442	AAATCATAGTTAAAG[A/G]CAAAGCATTAAAATA	23077
rs370191441	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77200597	CATAATTGTCAGATT[C/T]ACCAAAGTTGAAATG	23077
rs370195450	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77167217	TGTACATAAACATAT[A/G]TACATTTATGTATAT	23077
rs370200301	snp	C/G	3.31285e-05	0.00406978	missense	MYCBP2	GRCh38.p7	13:77176600	GATGTCCATCTGTGG[C/G]AATGAGTTGAATCTC	23077
rs370201129	snp	A/G	1.65578e-05	0.00287726	intron-variant	MYCBP2	GRCh38.p7	13:77121513	ACAATAAAAGCCATA[A/G]CTGTAACATTAGTTT	23077
rs370227728	snp	A/C	6.94252e-05	0.00589133	missense	MYCBP2	GRCh38.p7	13:77270538	TTAGAATTGTTGGCA[A/C]CTAATCAAAAGAGAA	23077
rs370244138	snp	A/G			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77077044	AAATGGGCAACATTT[A/G]TAGCCAGAAATTTCT	23077
rs370252300	snp	C/T	3.53582e-05	0.0042045	intron-variant	MYCBP2	GRCh38.p7	13:77211138	CTGCATCAAAACTTA[C/T]TGACTATTTTATAAA	23077
rs370264968	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77254732	ACTGTATTTTTGTAC[C/T]TATTAACCAACCACT	23077
rs370270066	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77195193	TTTCTCCAGCTCAGC[A/T]CTTATTCTCAACAGT	23077
rs370279729	snp	C/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77232729	GTAATGGCAGTCTTA[C/T]TATCATCATTTAATA	23077
rs370288803	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77284011	AAAACTTAATGTAGA[A/G]GCATTCAGGGAATAG	23077
rs370356352	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77304432	GCTAAAAAAGTTGAT[C/T]TCATAAAAGTAGAAA	23077
rs370363729	snp	C/G	1.72308e-05	0.00293515	intron-variant	MYCBP2	GRCh38.p7	13:77093144	ACTAGCTATTCAACA[C/G]ACAGGAGAGAACTAA	23077
rs370377727	snp	C/T	3.68378e-05	0.00429157	intron-variant	MYCBP2	GRCh38.p7	13:77260643	ATGTACAAATAATAA[C/T]AATAATGGTTTGTAT	23077
rs370382189	snp	C/T			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77078042	CAAGAAATGACCTGG[C/T]GATTTCTATGTGATT	23077
rs370399117	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77306613	TGAAAAGCTTTGGCT[A/G]TAGACCCTGCCTCAT	23077
rs370401180	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77260667	TTTGTATATAAAGCT[-/A]AAAAAAAAACCCATA	23077
rs370409949	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77124199	GCTGTACAACCATAG[A/T]CACGTTAGTTTAAAT	23077
rs370413688	in-del	-/A	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77305270	AAATACTGCACAGCC[-/A]AAAAATAGCAACAAC	23077
rs370430664	snp	A/G			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228727	TGTGTGTGTGTGTGT[A/G]TATACCATGTAACAC	23077
rs370451384	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77216801	ATGCCTGATCCTAGA[C/T]TGGAGGGGAAAGAAA	23077
rs370452028	snp	C/T	0.000280558	0.0118406	missense	MYCBP2	GRCh38.p7	13:77097750	GTCTCGGTTTTCCCA[C/T]CCTCACATTTTTCAT	23077
rs370459374	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77202380	AGACCAATAACAGGA[G/T]CTGAAATTGTGGCAA	23077
rs370463847	snp	G/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77159494	ATATATGAACTCTGA[G/T]ATGGTTTGGCTCTGT	23077
rs370470030	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77173478	TGAACTACATAGCTA[A/T]TTGCTGCCTGCTATT	23077
rs370474590	snp	C/T	9.90638e-05	0.00703719	synonymous-codon	MYCBP2	GRCh38.p7	13:77093206	CTCTGGCTCTTCAAA[C/T]ACATTAGGACTTGCA	23077
rs370480794	snp	C/T			upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77328392	AGACATGTGGAATCA[C/T]AGTATTTTAGTACTG	23077
rs370484623	snp	C/T	0.000153988	0.00877328	missense	MYCBP2	GRCh38.p7	13:77059546	CTGCATCAGAACAAA[C/T]ACTGCCAACAGCAGA	23077
rs370494020	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77050361	TATCTTATGTAAAAT[A/T]CTCTCCTATGGTTGC	23077
rs370495276	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77065745	GAGCATATTTTATTT[C/T]ATTAGATTTTAAAGT	23077
rs370496545	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77071251	TGTATATATATATAT[A/G]CATGCACGTGTGTGC	23077
rs370500650	snp	A/G	1.64803e-05	0.00287052	synonymous-codon	MYCBP2	GRCh38.p7	13:77180193	TCCACAGGTGTTAGA[A/G]ACGAGGTGGGAGGAG	23077
rs370528019	multinucleotide-polymorphism	GTA/TTT			intron-variant	MYCBP2	GRCh38.p7	13:77276667	GGGATTTTTTGGGGG[GTA/TTT]TTTTTTTGGTAGAGA	23077
rs370543937	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77321796	CTTGCACTTCCAGAT[A/G]GACAGTAAACTCAAG	23077
rs370547924	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77188703	ACTAGAAAAGCAAAT[C/T]GTTATTTGTTTCAAA	23077
rs370558587	snp	A/G	6.7348e-05	0.00580254	intron-variant	MYCBP2	GRCh38.p7	13:77188930	AAGAGAAAAGCTGAA[A/G]TTTTTTAAAACATGG	23077
rs370575075	snp	C/T	1.65059e-05	0.00287275	missense	MYCBP2	GRCh38.p7	13:77150736	TAAAATAAATTACCT[C/T]CATCATTGTTATGGC	23077
rs370579839	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77100665	TGTTTAATTGCAACA[C/T]GCCAATATTTAAGAT	23077
rs370595507	snp	C/T	1.64844e-05	0.00287087	missense	MYCBP2	GRCh38.p7	13:77166458	TCTGAACAGTTCTGA[C/T]AGGAATCAACAAACG	23077
rs370598387	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77269891	AGTAAAAATATATTA[C/T]CATTTCTGTTTAAAT	23077
rs370599018	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77049055	TGATTTTTCTCTTGG[A/C]TCCTATTTCTTTCCA	23077
rs370621222	snp	A/G	6.68729e-05	0.00578204	synonymous-codon	MYCBP2	GRCh38.p7	13:77211187	AATTACATCATATAC[A/G]GGATCAAGACACACA	23077
rs370630682	snp	A/G	1.65866e-05	0.00287976	missense	MYCBP2	GRCh38.p7	13:77169669	ATAAGGGGGAGCAGC[A/G]TGGAAAACAGACTGG	23077
rs370634675	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77146015	TTCTGCAAATCTATA[C/T]ATTATTATATGACAT	23077
rs370635870	snp	A/C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77278374	ACTAATTGAGAAATG[A/C/T]GTGTGCACGAACTTC	23077
rs370639868	snp	A/T	6.59152e-05	0.00574049	synonymous-codon	MYCBP2	GRCh38.p7	13:77125466	CCCTTCAGAATTGGT[A/T]ACCTGGTACATAACA	23077
rs370645855	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77122201	CAACTGGCTCCAAGA[A/C]TCTGTCTGATATAAA	23077
rs370663971	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77125956	TGAGACCTATGAATG[C/G]GAACAAAGAAATGAA	23077
rs370667662	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77184862	CCTCTCTCAGAATCA[C/T]TCACTCCAATTCAAA	23077
rs370673788	snp	A/G	4.94833e-05	0.00497385	synonymous-codon	MYCBP2	GRCh38.p7	13:77051847	ACAGGCACCACAAAT[A/G]AGCTCTCTGGGATCA	23077
rs370677233	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77222561	AGAGAGTGGTTCTCA[C/T]CCTGGATACATATAG	23077
rs370678076	snp	A/C			intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326402	AAGCACACACACACG[A/C]GGGTGCACGCGCGGC	23077
rs370683130	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77233562	CAAGAAGTTCAATTT[A/G]AATCAATCAAATTAT	23077
rs370686035	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77177562	CCTGTGCTCAAGTCA[C/T]CCAACTGCCTCAGCC	23077
rs370702547	in-del	-/T			intron-variant	MYCBP2	GRCh38.p7	13:77137606	TTTTTGTGTTTTTTT[-/T]GAGACAGAGATTCGC	23077
rs370705989	snp	A/G	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77094171	TCTGCTACACAAAGA[A/G]GACAATTTCCAAAAT	23077
rs370709629	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77274851	GTTAATTTCTTCCTC[C/T]CTTCTGTCTTCTTTT	23077
rs370725412	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77046075	TAAAAACATGAACAA[C/T]GTTATAAAATACAAT	23077
rs370764370	snp	A/G	3.30071e-05	0.00406232	missense	MYCBP2	GRCh38.p7	13:77174468	CATAGTTCCTCAAGC[A/G]CACAGCATATTTAAC	23077
rs370768841	snp	C/T	1.64732e-05	0.0028699	intron-variant	MYCBP2	GRCh38.p7	13:77140836	GGCTCTCAATTCATT[C/T]TGCCCTAACCTTATT	23077
rs370778014	in-del	-/TG			intron-variant	MYCBP2	GRCh38.p7	13:77166625	ACATCTGCATCTGTA[-/TG]TGTGTGTGTGTCTAT	23077
rs370784622	snp	C/T	3.29734e-05	0.00406025	missense	MYCBP2	GRCh38.p7	13:77067804	GGGATTTCACTCCTA[C/T]GATGCTGGCCAGACG	23077
rs370803139	snp	A/C	3.42015e-05	0.00413516	intron-variant	MYCBP2	GRCh38.p7	13:77191661	TATTGCTTAAGTAAC[A/C]CTTGGGCATTTACTT	23077
rs370809774	snp	A/G	3.30147e-05	0.00406279	synonymous-codon	MYCBP2	GRCh38.p7	13:77165288	CTCATCAGGTCCAGG[A/G]CTAAATTCATATCCA	23077
rs370811933	snp	C/T	4.95152e-05	0.00497545	synonymous-codon	MYCBP2	GRCh38.p7	13:77098931	TCCATCAGGTTTAAG[C/T]GATCTGCTGTGTTTA	23077
rs370818997	snp	C/T	0.000357882	0.0133721	intron-variant	MYCBP2	GRCh38.p7	13:77261151	TTTTTATTAAATGCA[C/T]AGTTGATCACTCAAC	23077
rs370839657	snp	A/G	1.65828e-05	0.00287943	intron-variant	MYCBP2	GRCh38.p7	13:77243202	AACAACAACATATAT[A/G]TTATATAATAGCTAT	23077
rs370841131	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77164640	CATTACTTTTGAAAT[A/G]AGAAGGAAGCACGTG	23077
rs370846515	snp	C/G	4.9889e-05	0.0049942	intron-variant	MYCBP2	GRCh38.p7	13:77144395	GATAAAAATAATTTT[C/G]ACTCTAGTTATTTGA	23077
rs370847849	in-del	-/TAAA	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77134916	ATTCTAAAACATGAG[-/TAAA]TAAACAAGACAGCAT	23077
rs370863085	snp	C/T	1.65037e-05	0.00287256	synonymous-codon	MYCBP2	GRCh38.p7	13:77068631	AAGCAGGGTTAGCTG[C/T]TGAGCCAGATATTGC	23077
rs370909379	in-del	-/T			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77294152	ATATACATATATATA[-/T]AAATATATATAAAGT	23077
rs370933034	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77152709	TCAGGGAAATATCAC[C/T]TTCTTCTCACACCAT	23077
rs370956440	snp	C/T	3.43601e-05	0.00414474	intron-variant	MYCBP2	GRCh38.p7	13:77121333	GGTAATAAAAAATAT[C/T]GAAGTTAGGTAAGTA	23077
rs370967546	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77178240	TCTTATCAGTCATAA[C/T]GTATGAATAAATCAT	23077
rs370969754	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77205700	TAAAATAAATAAACT[C/T]AGAATGTTACTCCAA	23077
rs370979081	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77200211	AAGGAGCTGATGGAG[A/C]TGAAAACCAAGGCTC	23077
rs370980789	snp	A/T			intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77074022	CCCCCCTTTTTTTTT[A/T]AAAGAAACGGTCAAG	23077
rs370991532	snp	A/G			intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075120	GGCTGAGACAGGAGG[A/G]TCCATTGAGCCCGGG	23077
rs370992928	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77298356	ACACTCTCATTCATC[A/G]TATATTTATGTTTCA	23077
rs371018243	snp	C/T	1.65329e-05	0.0028751	synonymous-codon	MYCBP2	GRCh38.p7	13:77270380	TCCATCATTCTGAAG[C/T]AGACATTGGTCATCT	23077
rs371019723	snp	A/C/T	3.29935e-05	0.00406149	missense	MYCBP2	GRCh38.p7	13:77166409	GAATTAAGATTTTCA[A/C/T]GAACAGATGTCAATT	23077
rs371057099	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77250537	ATGTAGAAAATAGAT[A/T]CAAAATTCTTCCTAA	23077
rs371068547	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77201508	AAGTCAACAAGGATA[C/T]CCAGGAATTGAACTC	23077
rs371075623	in-del	-/C			intron-variant	MYCBP2	GRCh38.p7	13:77210203	CAATAATTTTTTTTT[-/C]TTTTTTTTTTTTTTT	23077
rs371076433	snp	A/G			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77079147	TCCCTCTCCTTATTC[A/G]AAGTCTAAATATTCA	23077
rs371080820	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77248142	AACTTAAAGTATAAT[A/C]AAAAAAAAAAAAAGA	23077
rs371081406	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77275143	CAAAGAATGTCTCTA[C/G]CCTTTCAAAAAGGTT	23077
rs371090681	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77297665	GCCTGCTGGAAAAAA[A/C]GTAATGGGTTTGATT	23077
rs371090840	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77189547	AGAAAGAAAGATAGG[A/G]AGATAGAATCACAGT	23077
rs371102746	snp	C/T	3.29538e-05	0.00405904	synonymous-codon	MYCBP2	GRCh38.p7	13:77180247	GCTGTTCCTGACTGG[C/T]AGCACAACAATGACC	23077
rs371116053	snp	A/G	0.000153988	0.00877328	synonymous-codon	MYCBP2	GRCh38.p7	13:77097611	ACTTGGAAAAATCAT[A/G]TTCTGGGAAGCAGCT	23077
rs371118024	snp	C/T	0.000153988	0.00877328	intron-variant	MYCBP2	GRCh38.p7	13:77150965	TGTTAGCATTGGTC[C/T]	23077
rs371123822	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77053755	TTTCTGGCTATCATC[C/T]CTCTACTTAGACATC	23077
rs371128207	snp	A/T			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291588	CCAGCCTCCACATGG[A/T]GAAACCCCGTCTCTA	23077
rs371143304	snp	A/T	0.000186749	0.00966125	intron-variant	MYCBP2	GRCh38.p7	13:77146243	GAGACCAGTCTGAAC[A/T]ATCGTAAAATCATTT	23077
rs371159398	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77281582	TGCTCTCAAATAATT[A/C]AATTTTGAAGGTTAT	23077
rs371162741	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77229816	TATAATATTTTCATC[A/T]CACTGCACCATTTCC	23077
rs371198339	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77096797	AAGTATAAAAGTTCT[A/C]TAACAATGATATATT	23077
rs371205486	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77226448	ATCACTAACATATGA[C/T]CTTTATATCATCAAG	23077
rs371224062	in-del	-/C			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77086663	TCTAGATAATTTCTA[-/C]AGGTCTCTTATATTT	23077
rs371224735	snp	C/T	0.000539802	0.0164198	intron-variant	MYCBP2	GRCh38.p7	13:77251128	TCTGCACATGTTCTT[C/T]AGTAGGAATCATTGT	23077
rs371232979	in-del	-/G	0.00959509	0.0685965	intron-variant	MYCBP2	GRCh38.p7	13:77070727	CTTTACATAGAAAAA[-/G]AAAAAAAAAAAAAAG	23077
rs371261984	snp	C/G	3.29794e-05	0.00406061	synonymous-codon	MYCBP2	GRCh38.p7	13:77096342	AGCCTGTTTTTCGCG[C/G]AGGTATTTTTCTCTA	23077
rs371271450	snp	C/G			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77293489	ATACAAGGGAGATAT[C/G]GTAGGTAAATAATAG	23077
rs371283713	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77318703	AGGTTGCAGTGAGCC[A/G]AGATCGCACCACTGC	23077
rs371290441	snp	A/G	9.24616e-05	0.00679869	intron-variant	MYCBP2	GRCh38.p7	13:77288394	GAAATACAAAACAGA[A/G]TATTTCCATTTCACA	23077
rs371311366	snp	C/T	4.94214e-05	0.00497074	synonymous-codon	MYCBP2	GRCh38.p7	13:77168458	ACAGGCAGGTTTATA[C/T]GGGTGCTCACTCTCT	23077
rs371335659	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77249745	TCCAGGAGAATAAAT[A/T]TCAATTCCAACATTG	23077
rs371350567	snp	C/T	1.65652e-05	0.0028779	missense	MYCBP2	GRCh38.p7	13:77095421	TCAGAAATGCCTTCT[C/T]TTACACTGGGCAACT	23077
rs371362078	snp	G/T	0.000153988	0.00877328	synonymous-codon	MYCBP2	GRCh38.p7	13:77061734	ACATAAATTTCCACA[G/T]ACATTGCATAAAATG	23077
rs371370595	snp	C/T	0.000160464	0.00895578	synonymous-codon, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087523	TTTATTTTCTTCATC[C/T]TCTTCTTCCTCTGGT	23077
rs371397296	snp	A/C	0.0174175	0.0916809	upstream-variant-2KB, intron-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77327178	CCCCTCTCCGCCACC[A/C]CTCCCTCCGCCTCGG	23077
rs371397673	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77325664	GTTCTGCAGTTTTCC[C/T]CTTTTCCCTACAAAA	23077
rs371398697	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77178438	GTGAATTTGCAAGTA[A/T]AACTTCATTTGAAGA	23077
rs371418517	snp	A/C	4.94654e-05	0.00497295	missense	MYCBP2	GRCh38.p7	13:77217930	TGTGCTAGGGCCTGG[A/C]AATGCTTGAACAAGA	23077
rs371422206	snp	A/G	0.00058183	0.0170463	intron-variant	MYCBP2	GRCh38.p7	13:77164402	CCTTTTATAATACAT[A/G]CAAAACAAAACAAAA	23077
rs371446054	in-del	-/TCAAACTAGACATG			intron-variant	MYCBP2	GRCh38.p7	13:77306986	ACATTTGAAAAAAAA[-/TCAAACTAGACATG]AAAAATAACTGACAC	23077
rs371457906	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77223332	CTCTTAATGTTATGC[G/T]GGAACCTAGACTCCT	23077
rs371461362	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77062957	TCTTCTATCTGACAA[A/G]TAAAATTATCCTTTA	23077
rs371483740	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77188207	TCATTCCTACCAGGA[A/G]TATATATTCACTTGG	23077
rs371507870	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77303242	GGAGGCTGAGGCAGG[A/G]GAATCGCTTGAACCC	23077
rs371514332	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77246794	ACCATAACGAAGTGG[C/G]ATTTACTCCTGGAAT	23077
rs371526226	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77047998	CTAACCTCACCTTTG[C/T]ATCTGTGCTCCTTAA	23077
rs371527588	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77136053	CTTGAACTGCTAACC[G/T]TGTGATCCACCCGTC	23077
rs371538316	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77294922	TAACTCAGTCTAACC[A/G]AAGTATCCCGTATCT	23077
rs371548762	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77319938	TGCAGATGTGCACAC[C/T]GGAAGTTTATTGCGG	23077
rs371549099	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77186757	GCACTTACTGCCCCA[C/T]TCCCACCAAATCCCA	23077
rs371554123	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77122612	GGAGAATGGCATGAA[C/G]CTGGGAGGCGGAGCT	23077
rs371567103	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77216841	ATAATTATTAGGTCA[A/T]TTCACAAAATACAAA	23077
rs371574146	snp	C/G	3.31203e-05	0.00406928	intron-variant	MYCBP2	GRCh38.p7	13:77224444	CAAATGAAAAGTTAG[C/G]AAGTACCTGGAGTTG	23077
rs371575235	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77254325	GGGAGAAATGGAATA[C/T]GATAATAAGCCTTGG	23077
rs371575329	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77169395	ACAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	23077
rs371584721	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77194353	TGGACCATACCAAAT[A/G]TAAAAAATCAGAGTA	23077
rs371592082	snp	C/T	5.00271e-05	0.0050011	intron-variant	MYCBP2	GRCh38.p7	13:77139166	AACAGCGTGTATCTA[C/T]AATGCTTTTTAAAAC	23077
rs371592965	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77174901	AATATTAGCCATACT[A/T]TATATATATAATATA	23077
rs371611092	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77245853	ATATATATATGTATA[C/T]ACACACACACACATA	23077
rs371627279	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77251049	AGTGAAGATGCCACT[A/G]GTCTTTAAGAAAAAA	23077
rs371629812	snp	G/T	1.87485e-05	0.00306169	intron-variant	MYCBP2	GRCh38.p7	13:77058456	GTAAAAAAGCACACA[G/T]TCTGGTAATTTTCCT	23077
rs371636741	snp	C/T	1.65061e-05	0.00287277	missense, utr-variant-5-prime	MYCBP2	GRCh38.p7	13:77225534	TGCTTGCATCCTTTT[C/T]GCCTCTTTCTCCACT	23077
rs371670683	snp	C/T	1.6604e-05	0.00288127	synonymous-codon	MYCBP2	GRCh38.p7	13:77181821	TCCATCATACGCAAT[C/T]GGGAAGATGGAAGTC	23077
rs371681456	snp	A/G	0.000153988	0.00877328	intron-variant	MYCBP2	GRCh38.p7	13:77062711	AGCTGTTGAAAGGGA[A/G]GGCTGTTACACCACT	23077
rs371687613	snp	C/T	0.000153988	0.00877328	missense	MYCBP2	GRCh38.p7	13:77098266	TGAACTTTATTTGAA[C/T]CTTCATCCACACTCT	23077
rs371695445	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77115664	AAATTTCCAAAGATA[A/G]GTGTAAAAACTATGA	23077
rs371704019	snp	A/G	1.74439e-05	0.00295325	intron-variant	MYCBP2	GRCh38.p7	13:77206614	CCCTGGACAGCACAC[A/G]TTAATGTGAATTAAT	23077
rs371706876	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77192779	TGAAGAAATCCTAGA[C/T]GATTCTCTATAAATG	23077
rs371720729	snp	A/C/G	3.41747e-05	0.00413357	intron-variant, nc-transcript-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087652	AAGAAATGACGGTTA[A/C/G]ATGAGTTCAAGAATA	23077
rs371732115	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77289932	TCAAAAATAATAGCA[C/T]TGAAGTCACAGACTG	23077
rs371755393	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77305887	CAGATTTTACTTAAT[A/C]TAATACAGATTATCT	23077
rs371775112	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77153713	TGTATTTCCTATGTG[A/C]CTTTCTCTTGTCAAT	23077
rs371811849	snp	G/T	1.67584e-05	0.00289464	intron-variant	MYCBP2	GRCh38.p7	13:77174263	GTAGTAGACTGTGTA[G/T]GTTCTACCACTGTAA	23077
rs371821679	snp	A/G	1.73918e-05	0.00294883	intron-variant	MYCBP2	GRCh38.p7	13:77190206	ATTCTACTTCATTAT[A/G]GCAAAATAATAAACC	23077
rs371822880	in-del	-/A	0.0433465	0.140692	intron-variant	MYCBP2	GRCh38.p7	13:77105619	ATCTATACACAAAAG[-/A]AAAAAAGTTGATAGA	23077
rs371829428	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77236088	GCTAATGGCTTAGAA[A/G]ATAAGACTGGAGGTA	23077
rs371876519	in-del	-/GAG			intron-variant	MYCBP2	GRCh38.p7	13:77246554	AAGGAGGAGGAGGAG[-/GAG]CAGGAGGAGAAGGAG	23077
rs371891262	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77295423	AGGCGTGAGCCACTG[C/T]ACCCAGCCAATGATA	23077
rs371897268	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77272878	GTCTTAAGATCATAA[C/T]TTCTTTCTCAATTTC	23077
rs371905394	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77161383	AAACGAGCAAAAAAG[G/T]TAAAGCAAACAATAA	23077
rs371918031	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77111294	CCAACTGGAGCTAAG[A/T]CATCCAACCGAACTC	23077
rs371937237	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77244989	AAGACATTTATGCAG[C/T]CAACAAACGAAAAAA	23077
rs371964307	snp	C/G	0.000465601	0.0152507	intron-variant	MYCBP2	GRCh38.p7	13:77264050	ACAAGCAAACACCTT[C/G]CAAAATGAATTTACT	23077
rs371967933	snp	C/T	6.96662e-05	0.00590155	intron-variant	MYCBP2	GRCh38.p7	13:77181971	AAAATATAGCATCAG[C/T]ATAATCTAAGTTTCT	23077
rs372000674	snp	C/T	3.29783e-05	0.00406055	synonymous-codon	MYCBP2	GRCh38.p7	13:77251171	GGGGACTCTGTCTGG[C/T]CGTCCACTACTGACA	23077
rs372014600	snp	A/T	1.64768e-05	0.00287021	missense	MYCBP2	GRCh38.p7	13:77144527	ACAATAAGTCCCATC[A/T]TTATTGACACGGATC	23077
rs372015278	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77197997	AGATAAGGTCCACTA[C/T]GTTGTTCACTATTCC	23077
rs372016633	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77055484	AATAATTAGATATCA[C/T]TGTACAATTTGAATT	23077
rs372031998	in-del	-/ATT	0.00716266	0.059414	intron-variant	MYCBP2	GRCh38.p7	13:77130312	AATGAAACTTTTCTC[-/ATT]ATCTCATTTTAGATA	23077
rs372037284	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77133745	ACATAGCATGTCCCC[A/G]TAACTCTGAACATTT	23077
rs372044297	in-del	-/TGTA			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228726	GTGTGTGTGTGTGTG[-/TGTA]TACCATGTAACACTG	23077
rs372046418	snp	C/T			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77082561	AGTGTAAAAGCAATG[C/T]TAAATTCTCAACACA	23077
rs372051985	in-del	-/AT			intron-variant	MYCBP2	GRCh38.p7	13:77049415	TGAAATGGATAGTAT[-/AT]GTTTCACATGGTTTA	23077
rs372057713	in-del	-/ATAATA			intron-variant	MYCBP2	GRCh38.p7	13:77174929	ATATATTATATATAT[-/ATAATA]TATATATATTTTATA	23077
rs372069326	snp	C/T	0.000105852	0.00727425	intron-variant	MYCBP2	GRCh38.p7	13:77262168	CTATTGCATTTCTAA[C/T]ATGAAGAATTCTAAA	23077
rs372076584	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77052040	CATTATCTACTAGAC[C/T]ATCCCTTGAAATGCC	23077
rs372081264	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77278014	TCACTGATATGAAAG[G/T]CAAGAATCGGAACAT	23077
rs372117168	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77180607	ATTCTATATGACAGA[C/G]AGAAAACTTCTTTCC	23077
rs372121545	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77187679	GAAAACTGTAAGTAT[C/T]GTAAGAAACAAGCAA	23077
rs372124482	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77129146	TTATTGTTCCTTACA[A/G]TTAACTCACCTGGGG	23077
rs372127001	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77264565	ACTTTTTAAATGTTT[G/T]TCCAACAAGAGCAGA	23077
rs372157257	in-del	-/AAG			intron-variant	MYCBP2	GRCh38.p7	13:77225202	CTTGAATTATAAAAG[-/AAG]TCCACAGGAAGACAG	23077
rs372164925	snp	A/G			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076440	GAAGACAGTACTTTT[A/G]AGCTGAACTGTGAAG	23077
rs372220356	snp	A/C	1.78468e-05	0.00298715	intron-variant	MYCBP2	GRCh38.p7	13:77097329	GATCTGGTTCATTAA[A/C]GAAAAAAGCACTTAT	23077
rs372223660	snp	C/G/T	0.000131829	0.0081178	intron-variant	MYCBP2	GRCh38.p7	13:77070627	GAAATAGCTGTTAAC[C/G/T]AACCTGTTTTTGTAA	23077
rs372226581	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77089034	GAAGAACCAACTTCT[A/G]TTAAAGAAAAAGAAA	23077
rs372233408	in-del	-/G			intron-variant	MYCBP2	GRCh38.p7	13:77097088	CCACTGTTTCTGCTG[-/G]TGTGAGACAGACACA	23077
rs372249641	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77106245	GCAATGATTGGAAAT[C/G]TTAAATTTCATGAGT	23077
rs372256800	snp	C/T	1.65045e-05	0.00287263	missense, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77077330	TTTTTATGATGTGAT[C/T]ATCCCCTCCTGGAAG	23077
rs372271310	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77060640	ACATACATAGGTTAC[C/T]TTTTGTTTTATGTCT	23077
rs372301749	snp	A/C	1.64953e-05	0.00287182	missense	MYCBP2	GRCh38.p7	13:77158075	TGAGAAAGAGCTAGA[A/C]CCTTTCCAAGAATTC	23077
rs372301899	snp	C/T	0.000132111	0.00812639	missense	MYCBP2	GRCh38.p7	13:77098339	TTGTTTTTAAAGTAC[C/T]TGAGGTGCAGACTTC	23077
rs372351334	snp	A/G	6.90274e-05	0.00587443	intron-variant	MYCBP2	GRCh38.p7	13:77211938	TTGGAAGGGGCATTT[A/G]TTTATTTCTGGTATT	23077
rs372363588	snp	C/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77055944	AAGCCCATATTTTTC[C/G]AAGAGCAGGGAAAAT	23077
rs372412852	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77322881	TCCGATTTTGATTGG[C/T]CTCATTCATCCAAAA	23077
rs372422045	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77263901	GGAATTCCATTTACA[C/T]TAGCTACTTAAGATT	23077
rs372434186	snp	A/C/T	0.000799548	0.019981	intron-variant, nc-transcript-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087646	AGCCTGAAGAAATGA[A/C/T]GGTTAAATGAGTTCA	23077
rs372497777	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77139655	CTTCCTTCCCTTATA[C/T]TTATATTTTAAGAAA	23077
rs372501299	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77318549	TCACGAGGTGAGGAG[C/T]TCGAGACCAGCCTGA	23077
rs372568958	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77059260	AATACAGTTCATAAA[C/T]TTTTAACTGTTTCTA	23077
rs372569923	snp	C/G	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77287369	TTTGTATTTTTAGTA[C/G]AGACAGGGTTTCACC	23077
rs372574991	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77309171	TAAATACTCCCATGT[C/T]CAGCCTCACTTTCCC	23077
rs372591009	in-del	-/G	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77325127	AAACTGGTTAACCTA[-/G]AAAAAGTGTGAACAA	23077
rs372615358	snp	A/C	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77238533	AGCACTTCACTTGCA[A/C]AGTTAAATTAATACA	23077
rs372626725	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77262296	AACCATAGGTATAGT[A/T]CTCCAAGGAAAGATA	23077
rs372637222	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77312864	ACTAGTTGCCTAAGA[C/G]GAGAAACTTTAAATA	23077
rs372651340	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77106872	AAGCATTACCTGACA[A/G]TTCTTCAATCTTCAT	23077
rs372681229	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77138753	GCCGAGAAGGAAGAG[A/G]GTCAAAATTAGACAG	23077
rs372684766	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77199227	GGCATTGCCTCACTC[A/G]GGAAGCGCAAGGGGT	23077
rs372685334	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77154854	ATGCTTTTTGCATTG[C/T]ATAGAATAATTCCAA	23077
rs372689241	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77207447	ACCTCTTTTAGGGGT[C/T]GGGAAGTGAGGGATG	23077
rs372693691	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77129919	ACAGGCCTACTTTTC[C/T]CTATCTCAAAGTTTA	23077
rs372696724	snp	A/T	1.6838e-05	0.0029015	missense	MYCBP2	GRCh38.p7	13:77205566	CAACACCCATTTTTA[A/T]GTCCTGCATAGCTGC	23077
rs372702467	snp	C/G	1.6507e-05	0.00287284	missense, utr-variant-5-prime	MYCBP2	GRCh38.p7	13:77288189	ATAGGGGGCTCTTTG[C/G]ATTCCTCTTCTTCAT	23077
rs372713519	snp	C/T	1.65034e-05	0.00287253	intron-variant	MYCBP2	GRCh38.p7	13:77233114	AATGAGTGGAAGAAA[C/T]TGGGAAAGTATCCCA	23077
rs372749213	snp	C/T			intron-variant, downstream-variant-500B	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77088224	AAATCACATTTTACT[C/T]TGAAAATTCATTTTA	23077
rs372766769	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77185692	TCAGAATGACATGTA[A/T]TCTATTTTACTCTTT	23077
rs372767179	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77202942	CAGCCAGTATCATAC[C/T]GAATGGGCAAAAACT	23077
rs372770016	snp	C/T	3.32452e-05	0.00407695	intron-variant	MYCBP2	GRCh38.p7	13:77088821	CAGTAATTTCATTAA[C/T]GTCTTCATACCTCCA	23077
rs372771477	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77125168	GCATTAAGTACTCAC[A/G]TATTTTACAAACCAA	23077
rs372775457	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77089730	TGATGGCAGCTCCAA[C/G]AGTTATCAAGCTTCA	23077
rs372790848	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77137374	ATGAGCAAAGAAATC[A/T]GAGAAAATTTGGACT	23077
rs372799682	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77175228	GTGCGCTACTGTGCC[C/T]GGCAATAAGGGATTT	23077
rs372804709	snp	A/G	0.000376719	0.0137192	intron-variant	MYCBP2	GRCh38.p7	13:77051201	ACACAAGATCATAGT[A/G]AGACTATTTCAATCA	23077
rs372808544	snp	C/T	0.000976686	0.0220769	intron-variant	MYCBP2	GRCh38.p7	13:77189091	TGTTAGAAAGTCCAA[C/T]GTCATTTTTTCTTTT	23077
rs372819840	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77160440	AAAGATGAAATAAAT[A/G]TTTTCATTATTACCG	23077
rs372837844	snp	G/T	0.000153988	0.00877328	missense, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081617	ATGTCAACAATGCTG[G/T]TTAAGTCCTTTAAGC	23077
rs372839934	in-del	-/AACATAACATAACATAACAT			intron-variant	MYCBP2	GRCh38.p7	13:77317939	AAGACTCCGTCTCAA[-/AACATAACATAACATAACAT]AACATAACATAACAT	23077
rs372847961	snp	G/T	6.64883e-05	0.00576539	utr-variant-3-prime	MYCBP2	GRCh38.p7	13:77045366	TCTCTGTAGACAAAG[G/T]ATCTGCGTGTTCTAA	23077
rs372869743	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77155393	AAGACAACTTTGAAG[A/G]AGGAAAGGGCTGGGG	23077
rs372871064	in-del	-/ACACACAC			intron-variant	MYCBP2	GRCh38.p7	13:77245745	CCAGAACGTAAAGTA[-/ACACACAC]ACACACACACACACA	23077
rs372874238	snp	C/G	0.000306279	0.0123712	intron-variant	MYCBP2	GRCh38.p7	13:77126290	AAAATGAGTATCTTA[C/G]AAGTCATGAAGCTAC	23077
rs372885860	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77107318	GTTTATTGATTCTTA[C/T]AGACAATATATAAAT	23077
rs372887677	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77174894	CTGCTAGAATATTAG[A/C]CATACTATATATATA	23077
rs372910895	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77052655	TGAGAAATTTTTCTC[A/T]TTTTGAAATATTAAA	23077
rs372917179	in-del	-/AC	0.219049	0.248077	intron-variant	MYCBP2	GRCh38.p7	13:77070573	CAGACAAACAAACAA[-/AC]ACACACACACACACA	23077
rs372930550	in-del	-/GAAAG			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77292978	AAAAAAAAAAAAAAA[-/GAAAG]AAAAAAAAAGAAAAC	23077
rs372986609	snp	A/G	0.000171733	0.00926482	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77078795	TTCTCTCTAGGTAGC[A/G]AAACATTTAATGACA	23077
rs372987085	in-del	-/CACATACAGA			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076320	AAAATGAAGAAGAGA[-/CACATACAGA]TTATTATGAACTCCA	23077
rs373002519	snp	A/G	0.000153988	0.00877328	synonymous-codon	MYCBP2	GRCh38.p7	13:77270058	TGTAGAATTGTATAT[A/G]TGGCCCTGCAAAAAA	23077
rs373012467	snp	A/G	1.65029e-05	0.00287248	missense	MYCBP2	GRCh38.p7	13:77165304	CTAAATTCATATCCA[A/G]TTGCAAAACACTTAA	23077
rs373027602	snp	C/G	1.66026e-05	0.00288115	synonymous-codon	MYCBP2	GRCh38.p7	13:77098976	TTTTCCTGATGTAGA[C/G]GCTGGTTTAGAAGAT	23077
rs373027753	snp	C/T	3.29935e-05	0.00406149	missense, nc-transcript-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77083104	ATGGTCTGCAGCAAG[C/T]GGTGAAAGGTGTGTG	23077
rs373039956	snp	G/T	0.000493072	0.0156937	intron-variant	MYCBP2	GRCh38.p7	13:77051957	TACAGCAGGAAAAAA[G/T]AAAACTCTGGCATGG	23077
rs373040412	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77124001	CAAATGAACAGTTCT[A/G]CTGTTTCAGGACATT	23077
rs373053395	snp	A/G	6.65535e-05	0.00576822	intron-variant	MYCBP2	GRCh38.p7	13:77174288	CTGTAAAGTATTTCC[A/G]TTATCTCTATACATT	23077
rs373062870	snp	A/G	0.00167611	0.0289006	intron-variant	MYCBP2	GRCh38.p7	13:77095608	ATTGTTTGACCTGGC[A/G]AAGAAAAAAATCAAA	23077
rs373067865	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77315764	GTCAGGCATAGTGGC[A/G]TGTGCCTGTAATCCC	23077
rs373069851	snp	A/G/T	8.40462e-05	0.00648204	intron-variant	MYCBP2	GRCh38.p7	13:77177989	TTGTATCAGTAGTTG[A/G/T]TATACCTTTAACAAA	23077
rs373080461	snp	C/T	1.65002e-05	0.00287225	synonymous-codon	MYCBP2	GRCh38.p7	13:77098652	AGAACTAGCACCCGA[C/T]GGGCTAGACCTATTG	23077
rs373097361	snp	A/G	0.00233033	0.0340549	intron-variant	MYCBP2	GRCh38.p7	13:77045525	GAGGCAAAGGAAAAT[A/G]ATGTTTTAAGAATAC	23077
rs373099504	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77259670	TGTTCTACAGGTGTA[A/G]TTTCCCCAGCATGGG	23077
rs373116953	snp	A/G	1.6715e-05	0.00289089	intron-variant	MYCBP2	GRCh38.p7	13:77068544	CAAAAGCAATGGAAA[A/G]GCTGTAGTGTGATCA	23077
rs373118949	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77246261	TTTTAAAAGCAAGCA[G/T]TATAAACAATTTGGA	23077
rs373134767	snp	A/G	0.000214764	0.0103603	synonymous-codon	MYCBP2	GRCh38.p7	13:77121488	ATTCTGATCCAGAAG[A/G]GCTTGTTCTACAATA	23077
rs373144931	snp	A/G	1.65225e-05	0.00287419	synonymous-codon	MYCBP2	GRCh38.p7	13:77088973	AGAAAGAGAGCTGTG[A/G]GCTGAGATTAGCCGA	23077
rs373150640	snp	C/T	0.000440141	0.0148282	intron-variant	MYCBP2	GRCh38.p7	13:77058454	ATGTAAAAAAGCACA[C/T]ATTCTGGTAATTTTC	23077
rs373151240	in-del	-/T			intron-variant	MYCBP2	GRCh38.p7	13:77299012	ATTCTTCATACTWTT[-/T]TWRGAAACCAACTTT	23077
rs373166489	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77206038	TATTTATGATATGGT[A/G]ATTATATTTAGGAAT	23077
rs373166671	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77165932	TTCACACAAGAAAGT[A/G]GTTTACGAATTCTCT	23077
rs373174370	snp	C/G			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291300	CATCATTAGTCATTA[C/G]AGAAAAGCAAGCTAA	23077
rs373176576	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77214174	CAAATTAAAGGTACC[A/G]CAACACATTCTGTTG	23077
rs373177112	snp	C/T	3.89014e-05	0.00441012	missense	MYCBP2	GRCh38.p7	13:77296603	AGCAGCTTTACCTTG[C/T]TTCTTGTCTTCACTT	23077
rs373180863	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77174955	ATATTTTATATATTA[A/T]ATATATATATTTTTT	23077
rs373182682	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77279810	TTTATAATCTAATAG[C/G]GTAAATTAGTCATGC	23077
rs373197297	snp	G/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77319918	CCAGGAAACAGACTC[G/T]CAAATGCAGATGTGC	23077
rs373201127	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77252244	AATAATTTAGGCTCT[C/G]TGGCCCATACAAATC	23077
rs373215506	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77154417	AGGGAAGAAGAGAGG[-/A]AAAAAAAAAGCAGAT	23077
rs373238281	snp	C/T	6.75664e-05	0.00581194	intron-variant	MYCBP2	GRCh38.p7	13:77095642	ATCTTTTCTGACTTA[C/T]ATTAAAATCCTTAGT	23077
rs373242306	snp	C/T	0.000102698	0.00716507	synonymous-codon	MYCBP2	GRCh38.p7	13:77191801	CTCATCAAACATCAT[C/T]GCATATTTTTCTCTG	23077
rs373242870	snp	A/C/T	0.000165541	0.00909632	intron-variant	MYCBP2	GRCh38.p7	13:77066102	AACTACAAGAAAAAT[A/C/T]AGCACTTAAAAAGCC	23077
rs373265249	snp	C/T	1.74424e-05	0.00295312	intron-variant	MYCBP2	GRCh38.p7	13:77260629	AAATCAAGACCTCTA[C/T]GTACAAATAATAATA	23077
rs373265556	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77131358	CTCGTCTCTACAAAA[C/T]AATTTAAAAATATAG	23077
rs373272431	snp	A/G/T	1.64895e-05	0.00287132	missense	MYCBP2	GRCh38.p7	13:77166428	CAGATGTCAATTTTG[A/G/T]TCCATATCCTGAATT	23077
rs373272453	snp	G/T	0.000153988	0.00877328	intron-variant	MYCBP2	GRCh38.p7	13:77169598	ACATTCAAAGTTATA[G/T]AATTAAATTACACAC	23077
rs373274658	snp	A/C	1.64868e-05	0.00287109	synonymous-codon	MYCBP2	GRCh38.p7	13:77150941	AACAGGGACAGCTTT[A/C]ACTTCCACCTAAACA	23077
rs373274836	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77107908	TAGGAGGAATATGGA[A/C]TTATGTGAATGGTAA	23077
rs373275545	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77236514	TCTAAAATATTTTTA[A/G]AGGATTTCACCTCAA	23077
rs373276068	snp	A/G/T	8.5486e-05	0.00653732	intron-variant	MYCBP2	GRCh38.p7	13:77206643	ATGGTACATCAAATC[A/G/T]CAACCCTACCTAAAA	23077
rs373282966	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291597	ACATGGAGAAACCCC[A/G]TCTCTACTAAAAATA	23077
rs373283371	snp	C/T	3.76471e-05	0.00433845	intron-variant	MYCBP2	GRCh38.p7	13:77267964	AAAAAATTTTCCTGT[C/T]AAAATATTTATTACT	23077
rs373284997	snp	C/T	0.000877518	0.0209282	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77078900	TTATTCTGAAATAGA[C/T]AATTCACAATAGTTA	23077
rs373285836	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77049784	CGGATTACAGGTACC[C/T]GCCACCATGCCTGGC	23077
rs373289449	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77230999	TTAAATGACAAGACA[A/G]TGAGTGTAAATGGTT	23077
rs373306699	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77303268	AACCCGAGAGGTGGC[A/G]GTTGCAGTGTGCGTA	23077
rs373323088	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77095045	ACACACTTTCTTTAC[A/T]CTTCAGCATTTCGCA	23077
rs373326515	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77167618	AAATTTACATGATGT[C/T]TGCAGACATTAAATT	23077
rs373348275	in-del	-/G			intron-variant	MYCBP2	GRCh38.p7	13:77089647	CCAGATCATGTAACT[-/G]TTTTTTTTTTTTTTT	23077
rs373350885	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77211437	CAGAGAATAAAAGAG[A/G]CTAAGTAATTAAAAA	23077
rs373355617	snp	A/G	0.000153988	0.00877328	missense	MYCBP2	GRCh38.p7	13:77206818	GCTCTCTAGTATTTG[A/G]TCGAAACCTTTAAAG	23077
rs373362862	snp	C/G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77130793	ATCACTTTTTTTTAG[C/G/T]GTATTCTATTTTTTA	23077
rs373372501	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77199700	CTGGAGATCTGAGAA[A/C]GGGCAGACTGCCTCC	23077
rs373379032	snp	A/G	4.96866e-05	0.00498406	intron-variant	MYCBP2	GRCh38.p7	13:77121516	ATAAAAGCCATAGCT[A/G]TAACATTAGTTTCTT	23077
rs373386928	snp	C/G	8.24232e-05	0.0064191	intron-variant	MYCBP2	GRCh38.p7	13:77059495	GGGAACATGGACAAT[C/G]GGATGGCCTGTGTCA	23077
rs373406775	snp	C/T			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77079041	CCCTCCAACTAACCA[C/T]GGTTCCTATAACTTT	23077
rs373444704	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77112960	ACTTCTCTATACTCA[C/T]TGTCTCCAATTTCTC	23077
rs373447497	snp	C/T	1.64743e-05	0.00287	missense	MYCBP2	GRCh38.p7	13:77174402	TGAATGTCACACCAT[C/T]AGGGCACTGAACTGT	23077
rs373453210	snp	C/T			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77082668	AGGCTCTGTTTTCCC[C/T]AAGATTCTTTTCAAG	23077
rs373460327	snp	C/T	6.85248e-05	0.00585301	intron-variant	MYCBP2	GRCh38.p7	13:77140214	AACATAGAATAGAGA[C/T]CTTACAAGTAGCAAG	23077
rs373462099	snp	A/G	1.66807e-05	0.00288792	intron-variant	MYCBP2	GRCh38.p7	13:77188940	CTGAAATTTTTTAAA[A/G]CATGGCTTACCACTG	23077
rs373473643	snp	C/T	0.00993419	0.0697739	intron-variant	MYCBP2	GRCh38.p7	13:77058815	TATGGTGAAACCCCA[C/T]CTCTACTAAAAATAC	23077
rs373484896	snp	A/G	0.000181433	0.00952279	missense	MYCBP2	GRCh38.p7	13:77098915	TAGTCCGGCTCATAC[A/G]TCCATCAGGTTTAAG	23077
rs373490818	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77234695	AAAATGTAATAAAAT[A/T]GATATTTCAAATATG	23077
rs373492358	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77249133	AAGAATGAGGAGTCA[C/T]TGTTTAACAGTTACA	23077
rs373501431	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77274775	TCGCTTTTGCCCCAA[C/T]AGCCAGGGAGAATTT	23077
rs373504393	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77062848	TTCCTGATGTGGTAG[C/T]AGGCATACACGATCA	23077
rs373514613	snp	A/C			intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77325596	AATCTACGCGCTATT[A/C]AGATTTTCTAGCTAG	23077
rs373540930	snp	A/G	0.000115547	0.0076	intron-variant	MYCBP2	GRCh38.p7	13:77225430	CCTAAAGTTCCAGCC[A/G]CTACCTGAATGGTGA	23077
rs373547435	snp	C/T	1.66874e-05	0.0028885	intron-variant	MYCBP2	GRCh38.p7	13:77139385	TTCCTGTAAGTCCTA[C/T]GAGGCTAGCAAGGTC	23077
rs373559570	snp	A/G	1.65625e-05	0.00287766	intron-variant	MYCBP2	GRCh38.p7	13:77065956	TGTCAGCTTCCTGCC[A/G]CACTTCACTGCCAAA	23077
rs373568330	snp	A/G	1.6591e-05	0.00288015	synonymous-codon	MYCBP2	GRCh38.p7	13:77097935	TGTAGGTTGTTGGCT[A/G]TTTAAACTACTCCTT	23077
rs373580383	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77221983	TAAACACCATGTTAA[A/T]AGTTGTTATACTCTG	23077
rs373595823	in-del	-/TTATTT	0.0146672	0.084371	intron-variant	MYCBP2	GRCh38.p7	13:77270870	CTCGATCCATGTTTC[-/TTATTT]TATCTTCCATATTTC	23077
rs373598061	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77177227	AATTCTACTTTAAAT[A/C]TTTCTCTTTCTGAAA	23077
rs373616322	in-del	-/CA	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77071292	ACACACACACACACA[-/CA]CACACACACACACAC	23077
rs373621221	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77275444	TAAATGCTGTTATTT[C/T]TGCCTAGAGCACTTA	23077
rs373621541	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77307429	AGAAAAAAATGGTCC[G/T]GGCCTGGGCAACATA	23077
rs373630117	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77061044	ATTTAGTAAATATAT[A/G]GATCAATGATGTCAT	23077
rs373637205	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77245728	CGTTCTGCACATGTA[A/T]CCCAGAACGTAAAGT	23077
rs373647636	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77294584	TATCATATGCCACCA[C/T]TTCAGGAAAATCACC	23077
rs373670146	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77284060	TCAATGATTACTGAT[A/C]CGCAAAACACAAAAA	23077
rs373671441	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77218267	TACTCTGTATACTGA[C/T]TGGCCTGTTAGAGAT	23077
rs373686371	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77202106	TGAATCCAGGAGCTG[A/G]TTTTTTGAAAGGATC	23077
rs373703572	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77201470	CACCCCACTGTCAAC[A/T]TCAGACAGATCAACA	23077
rs373706389	in-del	-/A	0.00874735	0.0655527	intron-variant	MYCBP2	GRCh38.p7	13:77208756	CAGATACAGAGTATG[-/A]CCATCCTTTTTCCTG	23077
rs373730663	snp	C/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77276035	TTCCTCCATACGATT[C/T]ATCCACATTTGTAAT	23077
rs373740059	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77117012	AAATTTTCTAGTATA[A/C]ATTTTCTACCTGACT	23077
rs373757649	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77210190	ATATAAAGCACCACA[A/G]TAATTTTTTTTTCTT	23077
rs373804139	snp	C/G	1.64857e-05	0.00287099	missense	MYCBP2	GRCh38.p7	13:77166437	ATTTTGGTCCATATC[C/G]TGAATTCTGAACAGT	23077
rs373809573	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77126928	TTACTGCATTACTGT[A/G]TATTGTTATGGGTAA	23077
rs373810121	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77169795	GCTGTACTAAATCTA[C/T]ATTCTGCTCTTTTGA	23077
rs373814105	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77105599	AATCTATGAGATACA[C/T]TGATATCTATACACA	23077
rs373818917	snp	A/G	3.37935e-05	0.00411043	missense, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087548	TCTGGTTCCACTGGT[A/G]CAGGAGTCAGTGATG	23077
rs373822012	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77121744	TTATGAAGCCAATTT[A/G]CTTTTATTGTGGCAG	23077
rs373823546	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77241973	ATCAAAATTTTGCCT[A/G]TTGGAGGAATAAAAT	23077
rs373842786	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77277616	TTAGACTAAAACTTG[A/G]TCCTTTTTTTCCGAC	23077
rs373845613	snp	C/T	1.77347e-05	0.00297776	intron-variant	MYCBP2	GRCh38.p7	13:77097344	AGAAAAAAGCACTTA[C/T]ACGTACATTCAACAG	23077
rs373847200	snp	C/T	0.000115646	0.00760327	synonymous-codon	MYCBP2	GRCh38.p7	13:77270416	AACAGATATTTCTTT[C/T]AATGGCCACTTGTGC	23077
rs373848002	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77207219	TCCTCAATGTATAAG[A/G]GCTAGAAACAATCAA	23077
rs373854372	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77046006	AGGCCAATGATTCCT[A/G]TAATTTTTAAAAGTA	23077
rs373855283	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77186659	GCATATGAGTTTAAG[A/G]TGGTAGATTTTCTTT	23077
rs373856491	snp	C/T	1.648e-05	0.0028705	synonymous-codon	MYCBP2	GRCh38.p7	13:77070703	TTTCAGGTCAGCATC[C/T]GATGTTGCCTTTACA	23077
rs373866521	snp	A/C	0.000153988	0.00877328	intron-variant	MYCBP2	GRCh38.p7	13:77093142	ACACTAGCTATTCAA[A/C]AGACAGGAGAGAACT	23077
rs373873724	snp	C/G/T	4.96096e-05	0.00498024	splice-acceptor-variant, intron-variant	MYCBP2	GRCh38.p7	13:77233265	AAATACAAGGGGGCC[C/G/T]GAGGAGAAACATTTT	23077
rs373879730	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77200499	GAGAACTTCCCCAAT[C/G]TAGCAAGGCAGGCCA	23077
rs373889859	snp	A/T	0.00438332	0.0466095	intron-variant	MYCBP2	GRCh38.p7	13:77128073	AAATAAATGTAAAAT[A/T]CGCATTTTATATACT	23077
rs373925934	snp	C/T	0.00101315	0.0224844	intron-variant	MYCBP2	GRCh38.p7	13:77089077	CATAGGCAGTGCATA[C/T]ATATTTAAGATAATA	23077
rs373926392	snp	A/G			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77086849	ATCTCAAAACTAAAA[A/G]TATCAATTATACTTA	23077
rs373964746	in-del	-/TCT	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77274858	TCTTCCTCCCTTCTG[-/TCT]TCTTTTCTTTCCCCC	23077
rs374024718	snp	A/C	4.14688e-05	0.00455332	synonymous-codon, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326620	GGCGGGTAGCCCCAG[A/C]CCCAGCCCCGCAGCA	23077
rs374080860	snp	C/T			intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326092	CACTGTTGCAATTCT[C/T]TTCGTGTATCATCCT	23077
rs374083338	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77315894	GCAAGGCTCTGTCTC[-/A]AAAAAAAAAAAAAAA	23077
rs374094798	in-del	-/A	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77177257	AGTACAAAAAATATG[-/A]AGCAGTAGTGACCCA	23077
rs374103444	snp	C/T	6.37816e-05	0.00564683	intron-variant	MYCBP2	GRCh38.p7	13:77118550	CATTAACATCCAAAA[C/T]GGCAAAGTAAATGGT	23077
rs374122731	snp	C/G	0.000153988	0.00877328	intron-variant	MYCBP2	GRCh38.p7	13:77156034	GTATATAGATGTCTG[C/G]TAATTTAATCCAGTT	23077
rs374147981	snp	A/G	3.47373e-05	0.00416743	intron-variant	MYCBP2	GRCh38.p7	13:77211156	ACTATTTTATAAACT[A/G]AGATGCTTACCTCCA	23077
rs374161549	snp	G/T	4.94548e-05	0.00497242	missense	MYCBP2	GRCh38.p7	13:77096349	TTTTCGCGGAGGTAT[G/T]TTTCTCTACAGCGAT	23077
rs374218845	snp	C/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77285543	TGTAATCCCAGCACT[C/T]TGGGAGGCCAAGGTG	23077
rs374228593	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77248235	TACCAAAGGCACAGG[C/T]GACAATAACCAAAAA	23077
rs374229415	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77271817	CATCTCTATCAGCAG[C/T]GTGAAAACGGACTTA	23077
rs374230147	snp	A/C	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075486	CCCATTCTCTCTACT[A/C]ATCTCATTTGAATCC	23077
rs374230158	in-del	-/AT	0.0146672	0.084371	intron-variant	MYCBP2	GRCh38.p7	13:77105473	TGCTGAAAACAACAC[-/AT]GTTCTACACATTAAA	23077
rs374242789	in-del	-/A	0.883099	0.162184	intron-variant	MYCBP2	GRCh38.p7	13:77217965	GACATCCCCTAGGTT[-/A]AAAAAAAAAAAAGTA	23077
rs374244427	snp	A/C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77315842	AGAGGCTTCAGTGAG[A/C/G]CGAGATTATGCCACT	23077
rs374244751	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77200267	CCTCAGGAGCCGATG[A/C]GATCAACTGGAAGAA	23077
rs374253523	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77319426	AGCATAGCTGAGAGA[G/T]AATTCTACCTACCTT	23077
rs374254799	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77114514	AACATAGTACTTTAG[G/T]GTGTTCATATTCTCA	23077
rs374256378	in-del	-/T			intron-variant	MYCBP2	GRCh38.p7	13:77174952	TATATATTTTATATA[-/T]TATATATATATATTT	23077
rs374293878	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77183850	ACCGTGCCCGGTGAA[A/C]CCCTATTTCACTTTT	23077
rs374313272	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77133359	TTAAACAGAATGATC[A/G]TATCAAATGCAAAGA	23077
rs374320270	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77196379	GAAGAGACAATGATG[C/T]AATCTGTTGTACATT	23077
rs374370943	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77185042	AACTGCAATTTATTT[C/T]CTTGAAGAGTATTAA	23077
rs374377264	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77063600	AACTGTTTTCAGAAA[C/T]AGTTAAAAATTTCTG	23077
rs374396426	snp	C/T	4.07407e-05	0.00451317	intron-variant	MYCBP2	GRCh38.p7	13:77177709	AATCCTGATACACAA[C/T]CCACTAATCAGGATA	23077
rs374398514	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77051666	TAATATATATGAAAT[A/C]ATGTGAAAAATTATA	23077
rs374409620	snp	A/G	0.000132848	0.00814902	intron-variant	MYCBP2	GRCh38.p7	13:77146146	TTTGGTTATACTTTG[A/G]GAAAACGATCCTTAC	23077
rs374423721	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77262672	CTTATATAGCTACTC[C/T]ATCAATTCAAATATA	23077
rs374426018	snp	C/G	1.65018e-05	0.00287239	missense, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77077300	TCAGTGTATTTTCTG[C/G]GCCTTTTAATTCAAT	23077
rs374435633	snp	A/C/G/T	0.000263622	0.0114779	missense	MYCBP2	GRCh38.p7	13:77171533	AGGTCCTTAGAGGCT[A/C/G/T]GAACGACAGTGCTTA	23077
rs374438930	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77271606	TGCTGTTCTCATGAT[A/G]GCGAATAAGCCTCAC	23077
rs374459658	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77132045	AAAATTAAGAATAGC[A/G]TATATATATTATTAC	23077
rs374475747	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77046944	GGATGGGGACACTCA[A/G]TGGCAGATCTAGTTC	23077
rs374476996	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77059002	AAAAATAAAAAATAA[A/G]AAAAGTTCCCCAATG	23077
rs374477882	in-del	-/T			intron-variant	MYCBP2	GRCh38.p7	13:77174910	CATACTATATATATA[-/T]AATATATATTATATA	23077
rs374483186	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77095802	ATCAAACACAAACTA[C/T]ACTTCCTTTCCTTCT	23077
rs374491274	snp	A/T	5.05872e-05	0.00502902	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081383	GCATGAATACTAAGA[A/T]CTGAAAAGAGCTAAA	23077
rs374493937	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77122625	AACCTGGGAGGCGGA[G/T]CTTGCAGTGAGCCGA	23077
rs374509126	snp	A/G	0.000153988	0.00877328	intron-variant	MYCBP2	GRCh38.p7	13:77061152	TAAAGGCATGGCTCA[A/G]TCTTTAAACCTTTTA	23077
rs374511779	snp	G/T	1.68863e-05	0.00290566	intron-variant	MYCBP2	GRCh38.p7	13:77121352	GTTAGGTAAGTAAAA[G/T]ACTTACTTTTAAATA	23077
rs374531490	snp	C/T	1.67044e-05	0.00288997	missense	MYCBP2	GRCh38.p7	13:77055712	CTTCTGACATCCTCA[C/T]AGAGTTCTTTTATTG	23077
rs374541044	snp	A/G	2.07329e-05	0.00321963	intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326457	GGGGCGCAAGGAAGG[A/G]CACCCTGGGGACGCA	23077
rs374548954	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77153784	CAGGAAGTTTCAAAA[A/G]TAGATGAAATGTCCT	23077
rs374556131	snp	C/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77071018	TATTAGTTCACATCC[C/G]ACATTTAATTGTTTG	23077
rs374562517	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77048156	GAGGTGATGAGGTCA[C/T]GGGGTGGAATCCATG	23077
rs374566013	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77134157	AAGATTAGAAAAAAA[-/A]TGGAAGTGAAACCAT	23077
rs374583670	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77152831	AGCACTTTTGGAGTC[C/T]GAGGCGGGCGAATCA	23077
rs374583679	snp	A/G			missense, utr-variant-5-prime	MYCBP2	GRCh38.p7	13:77288232	CTCCACTCTGCACAG[A/G]GTTCTTAGATGCGGC	23077
rs374600562	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77060091	GAATTCCTACCTCAG[A/G]AACTCTGCAATTTGA	23077
rs374616566	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77189114	TTTCTTTTTAAAGTA[C/T]ATTATACATTTTTGA	23077
rs374618095	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77152779	CGTTTGATAAAATCC[A/G]CCGTGGCTGGGCGCG	23077
rs374625362	snp	A/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77197360	AGAAAGAGATATAGG[A/T]GGCCTATCAAGAAAA	23077
rs374641618	snp	C/T	0.000153988	0.00877328	intron-variant	MYCBP2	GRCh38.p7	13:77139160	AAAACAAACAGCGTG[C/T]ATCTATAATGCTTTT	23077
rs374649668	snp	C/T	4.96151e-05	0.00498047	synonymous-codon	MYCBP2	GRCh38.p7	13:77095477	GTAACACAGAATGCT[C/T]GGTTCTGCTGCACTG	23077
rs374652237	snp	A/G	0.000153988	0.00877328	missense	MYCBP2	GRCh38.p7	13:77061750	ACATTGCATAAAATG[A/G]TTGCTGCAGTTTCAC	23077
rs374655730	snp	C/T	1.64906e-05	0.00287142	missense	MYCBP2	GRCh38.p7	13:77212025	TAAGTGCTTCATCAA[C/T]TCGTAAAAAAGTTTG	23077
rs374664360	snp	C/T	9.94365e-05	0.00705042	missense, intron-variant	MYCBP2	GRCh38.p7	13:77126479	CTTGTTCTTGCATTG[C/T]TGCTTCCTGTGGGCA	23077
rs374707190	snp	A/C/G	0.000232597	0.010782	intron-variant	MYCBP2	GRCh38.p7	13:77121534	ACATTAGTTTCTTAC[A/C/G]TGCTATTCCCTATTC	23077
rs374708705	snp	A/G	3.41122e-05	0.00412976	intron-variant	MYCBP2	GRCh38.p7	13:77093154	CAACAGACAGGAGAG[A/G]ACTAAAATACCTTGG	23077
rs374719205	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77146581	TGCATCCATAACATA[G/T]AGAGAATAAATCCAT	23077
rs374721826	snp	A/C/T	4.94395e-05	0.00497169	intron-variant	MYCBP2	GRCh38.p7	13:77059512	GATGGCCTGTGTCAC[A/C/T]ATATACTCACCTGGC	23077
rs374723349	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77123485	GCATGGAAGGCATTT[C/T]GCATTTTAACAATAA	23077
rs374726501	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77096863	TAATATGTAGACAAA[C/G]AAAAAAATTAACCAA	23077
rs374736886	snp	A/T	0.00062433	0.0176572	intron-variant	MYCBP2	GRCh38.p7	13:77057145	AATAATGATAAACAG[A/T]TGAGTGACTGGGAGA	23077
rs374737921	snp	C/T	0.000153988	0.00877328	intron-variant	MYCBP2	GRCh38.p7	13:77174273	GTGTATGTTCTACCA[C/T]TGTAAAGTATTTCCG	23077
rs374762361	snp	C/T	9.89625e-05	0.0070336	missense	MYCBP2	GRCh38.p7	13:77261216	ATCCTGTAAAGAATA[C/T]GCTCCCATCTTCTGC	23077
rs374766943	snp	C/T			upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77328320	AAATAATGGATGGAT[C/T]TCATTTAGTTTTTTT	23077
rs374781457	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77154627	TATTAGAATGTTGTC[A/G]CATGAATAAAAAACT	23077
rs374786546	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77141337	TTGTGAGAAGCTGAG[C/G]TTCTCATGTTAGACT	23077
rs374790892	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77117821	TGTGAATTACTATCA[C/T]GAATGAAGGACTAGA	23077
rs374808776	in-del	-/ATCT			intron-variant	MYCBP2	GRCh38.p7	13:77138987	TACTACTTCCTGCCT[-/ATCT]GTGATGGATCATAAT	23077
rs374827981	snp	C/T	0.000384162	0.013854	intron-variant	MYCBP2	GRCh38.p7	13:77273694	AATAGAATTCAATTA[C/T]ATTCATCCAACATAC	23077
rs374829463	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77296864	ATTGAGAAGATAACA[C/T]GGGGCAGCTAAGCAA	23077
rs374854839	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77203477	CATACTGCCCAAGGT[A/C]ATTTACAGATTCAAT	23077
rs374855029	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77174895	TGCTAGAATATTAGC[C/T]ATACTATATATATAT	23077
rs374855247	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77091206	CTTATGTACATTCTT[C/G]TTTGAATAGACTATA	23077
rs374860061	snp	C/T	1.66413e-05	0.0028845	synonymous-codon	MYCBP2	GRCh38.p7	13:77166540	CATCCACCTCACACA[C/T]TCTGGGAATGTCACC	23077
rs374869936	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77166123	TTTCACAAAATCCTT[A/G]AAACATTGTCTTCTC	23077
rs374883170	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77061437	AATATTTCCAATCTT[C/G]TCTTTAATCTTCACA	23077
rs374910231	snp	C/T	0.000245313	0.0110723	intron-variant	MYCBP2	GRCh38.p7	13:77191629	TTTCAAAACAATATT[C/T]CTCTAACAAAAATAA	23077
rs374913077	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77184716	TGTGGCTTCCTCATG[A/C]ATGAATGAACAATGC	23077
rs374914298	snp	C/T	1.65649e-05	0.00287788	synonymous-codon	MYCBP2	GRCh38.p7	13:77189047	ATCACTGGTTGGAAG[C/T]CTAAAGGCAGTAGAC	23077
rs374919204	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77052000	GGGCATAGTGAAAGT[A/G]AGATCTAGGGGTTTT	23077
rs374923387	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77161425	AATGATGGCTCCCAA[A/T]TGTCTACAGGCAACT	23077
rs374925672	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77289733	AAGGGAAAAAGGCAA[C/G]AAGTATTTTCTAAAA	23077
rs374931740	snp	A/G	3.29973e-05	0.00406172	synonymous-codon	MYCBP2	GRCh38.p7	13:77098736	TTCAGCTCTGGAGCT[A/G]GAAGGCATCCTCCCA	23077
rs374933749	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77324504	AATCATCAATAGAGT[A/T]GTTGCAGGCTACTTT	23077
rs374947496	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77089945	ATTTAGAGATGCACA[C/T]TTATAGCTATGTCAT	23077
rs374961577	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77174904	ATTAGCCATACTATA[A/T]ATATATAATATATAT	23077
rs374971761	snp	A/G	3.29462e-05	0.00405857	synonymous-codon	MYCBP2	GRCh38.p7	13:77168506	GGAGGTTGTACAAGC[A/G]GAGAGGCCCTGTTCA	23077
rs374982453	snp	G/T	0.000280859	0.011847	synonymous-codon	MYCBP2	GRCh38.p7	13:77088865	ACAAGCAGATTTCCT[G/T]AGGGCCTGTTTCATT	23077
rs374987058	snp	C/T	1.65209e-05	0.00287405	missense	MYCBP2	GRCh38.p7	13:77176538	TGATCTCAGCTATAT[C/T]ACTGGGTGAGTCATC	23077
rs374999696	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77191539	TGGCATGAGGTTACA[A/T]GAATTTAATTTTTAG	23077
rs375003621	in-del	-/CACA			intron-variant	MYCBP2	GRCh38.p7	13:77071271	ACGTGTGTGCACACG[-/CACA]CACACACACACACAC	23077
rs375019450	snp	A/T	0.000299142	0.0122263	intron-variant	MYCBP2	GRCh38.p7	13:77243210	CATATATGTTATATA[A/T]TAGCTATGACAGAAC	23077
rs375028868	snp	A/C	1.6571e-05	0.0028784	intron-variant	MYCBP2	GRCh38.p7	13:77144415	TAGTTATTTGAAGTA[A/C]GTAGTAGCTCATGGC	23077
rs375055687	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77141835	AATGCACAATAAATG[C/T]TAGCTATTATTATTA	23077
rs375098777	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77113763	TCACTGAGAAGATGG[C/T]TCAGCTCAGTGAAGA	23077
rs375109692	snp	C/G	0.00159617	0.0282053	intron-variant, downstream-variant-500B	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77088148	AGTTAATAATTTGGG[C/G]TTTTAATTTAAAAAA	23077
rs375128713	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77050635	TTCATTTTATGGCAA[C/T]GGTTCCAGGCTTCGT	23077
rs375132774	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77059761	TGACAGTTTTAGAAC[A/G]GAAGGTTTCTAAGTT	23077
rs375137786	snp	A/C/G	0.000781082	0.0197479	intron-variant	MYCBP2	GRCh38.p7	13:77164405	TTTATAATACATACA[A/C/G]AACAAAACAAAACCC	23077
rs375138500	snp	C/T	0.0138799	0.0821421	intron-variant	MYCBP2	GRCh38.p7	13:77210942	GACACAGAAAGCAAG[C/T]TGTGGAGCTGGGATA	23077
rs375138614	in-del	-/AAT			intron-variant	MYCBP2	GRCh38.p7	13:77050934	ACAGAGCTTTCATAT[-/AAT]GTTTACATAAAACTA	23077
rs375160543	in-del	-/ACCC			intron-variant	MYCBP2	GRCh38.p7	13:77064132	TCCTCAAAGATTTCC[-/ACCC]TGACCCTGCCCTGGA	23077
rs375164087	snp	A/G	1.89038e-05	0.00307433	intron-variant	MYCBP2	GRCh38.p7	13:77174530	TTTTATTCACAATGT[A/G]CAGAGGATATATAAA	23077
rs375166187	snp	G/T	1.66568e-05	0.00288585	synonymous-codon	MYCBP2	GRCh38.p7	13:77057004	GCAAATGGGACAAGA[G/T]ATAAATCCAAATGTT	23077
rs375170846	snp	C/T	1.64768e-05	0.00287021	synonymous-codon	MYCBP2	GRCh38.p7	13:77140921	TTTTGGTGGGTCTTT[C/T]ACTTTTACTTCCAGA	23077
rs375180723	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77320150	TACACTGTATAGATA[A/T]TAGATGTAAACTGCC	23077
rs375191988	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076549	AGGTATAGAGCAAAT[G/T]TGCTGTTACTTAAAA	23077
rs375197836	snp	A/C/T			intron-variant	MYCBP2	GRCh38.p7	13:77199216	AAGCAGGGCGAGGCA[A/C/T]TGCCTCACTCGGGAA	23077
rs375218951	snp	A/T	0.000153988	0.00877328	intron-variant	MYCBP2	GRCh38.p7	13:77224570	TATTTTTTCATTATA[A/T]GCATTTTACATTTCT	23077
rs375236072	snp	C/T	0.000153988	0.00877328	synonymous-codon	MYCBP2	GRCh38.p7	13:77139310	CTCATCATTCAGCCT[C/T]AGCCACACACCATCA	23077
rs375243739	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77183537	ATAGTGATAGTCCCT[A/T]TTTCTTTTTTTTTTT	23077
rs375248261	snp	C/T	0.0422008	0.138995	intron-variant	MYCBP2	GRCh38.p7	13:77202743	GGATGGTTCAATATA[C/T]GCAAATCAATAAATG	23077
rs375263043	snp	A/T	0.000153988	0.00877328	intron-variant	MYCBP2	GRCh38.p7	13:77262030	AGAGAATGCTCATTT[A/T]TAATCCAAAGAGAAT	23077
rs375265207	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77177277	GTAGTGACCCAAGGT[A/G]GAAAGATGGAACACA	23077
rs375268001	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77305059	GGATGGCTTTGTTGG[C/T]GAATTCTTCCAAATA	23077
rs375297699	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77061476	TTTTTTATAAATGGA[A/G]AAATTAAGTGTTTCT	23077
rs375314778	snp	C/T	4.94238e-05	0.00497086	synonymous-codon	MYCBP2	GRCh38.p7	13:77144497	GAGTCCAATAGCCCC[C/T]GGAGTCCAATTTGCA	23077
rs375353115	snp	A/G	1.64833e-05	0.00287078	missense	MYCBP2	GRCh38.p7	13:77066008	GCTGCCATATCCTTG[A/G]TAAGTTTAATGATGA	23077
rs375373359	in-del	-/AAAAAGATTTC	0.0271762	0.113356	intron-variant	MYCBP2	GRCh38.p7	13:77057813	TGCCTAGTGATATAA[-/AAAAAGATTTC]AAAAAGATTTCAATC	23077
rs375375640	snp	C/T			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228812	TATGTACACATTATA[C/T]ATAATTATATACACA	23077
rs375382406	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77079334	TTTGAAGTAGGATAT[A/G]TGAGAGGAGGTTCTA	23077
rs375398778	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77275504	TCTAAATCTCATATG[A/T]CACATCTTCAGGGAG	23077
rs375406066	snp	C/G			upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77327291	TAAGGAAAGTGCTGG[C/G]GAGGCTGTCAGCTAC	23077
rs375406262	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77071252	GTATATATATATATG[C/T]ATGCACGTGTGTGCA	23077
rs375406442	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77250609	CATATTAACTGTAAA[C/T]TGACAATAATATAGA	23077
rs375460794	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77054049	GTGGTGTTGATGGAA[A/G]TGAGATGGGGGTATG	23077
rs375467184	snp	A/G	1.65809e-05	0.00287926	intron-variant	MYCBP2	GRCh38.p7	13:77205460	AACATTTCCTAAACC[A/G]AAGTATACATACTTT	23077
rs375482116	snp	A/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77094391	CAGTAATGCACTTTT[A/T]TCTAGTCTCCACATT	23077
rs375483472	snp	A/C/T	0.00714183	0.0593296	missense	MYCBP2	GRCh38.p7	13:77251194	TACTGACACAGCTGG[A/C/T]TCCATAACCTGTACA	23077
rs375488455	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77200560	CACAAAGATACTCCT[C/T]GAGAAGAGCAACTCC	23077
rs375513411	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77062850	CCTGATGTGGTAGCA[C/G]GCATACACGATCACT	23077
rs375531837	snp	C/T	3.30409e-05	0.0040644	synonymous-codon	MYCBP2	GRCh38.p7	13:77176563	GTCATCCGTTGTGTA[C/T]GTTCCTTTCACTAAT	23077
rs375535435	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77117642	TCATTCAATTAATGT[A/G]TTTATATATTGTATA	23077
rs375544582	in-del	-/T			intron-variant	MYCBP2	GRCh38.p7	13:77047012	GCCCTTGGGTTTTTT[-/T]CAAGGAAAAAATGAG	23077
rs375553875	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77286530	AGGCCGAGGCAGGCG[A/G]ATCACGAGGTCAGGA	23077
rs375557921	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77237123	TATTACAGTAAAACC[C/T]ACAAAAACTTACAAT	23077
rs375568605	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77289108	CAATAATTAGAGTAT[A/G]TCCAGGAAGTATCTA	23077
rs375571804	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77282811	TTCAGTAAAGGCCCT[C/T]ACCACACAAAACCTT	23077
rs375578898	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77312360	AGTTCTATAAAGTAC[A/T]CATGACTGTCGACAA	23077
rs375598534	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77148295	TTTAACAGCCAGTGG[A/T]CAATTCACCTAGAAC	23077
rs375616114	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77164877	TTACTCAGAAAGGTA[C/T]AGCCAACTGAGCAGG	23077
rs375634583	snp	A/C/G	0.000248514	0.0111446	intron-variant	MYCBP2	GRCh38.p7	13:77263641	GAAAACACTTAATTT[A/C/G]CTATCTTACTTATAA	23077
rs375639279	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77309884	TTTGGGAGGTCGAGG[C/T]GGGCAAATCACGAGG	23077
rs375648188	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77286785	AAAAAAAAAAAAAAA[A/T]AAAAATATATATATA	23077
rs375648665	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77190151	ATAATTTGCTGAATG[C/T]TTCAAATAATTTCTC	23077
rs375657146	snp	A/G	0.000153988	0.00877328	intron-variant	MYCBP2	GRCh38.p7	13:77288154	TTAATAGAACTCAGT[A/G]GCTTACCTTTGGAAG	23077
rs375658084	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77047697	CAGAAAAACCTTCAA[C/T]CAGATAAAGGACAAG	23077
rs375661939	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291613	TCTCTACTAAAAATA[C/T]AAAATTAGCCGGGCG	23077
rs375698865	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77183505	AGGCTGAAAAATTCA[C/G]CAGTATAAAGTTGTT	23077
rs375700885	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77201751	ATCTCACTCAAAACC[A/G]CTCAACTACATGGAA	23077
rs375713281	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77254464	CTTTCCTGGTTTAAA[C/T]AAACTTTTAAAATAT	23077
rs375717825	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77282323	GCTGAGGCAGGAGAA[C/T]CACTTGAACCCAGGA	23077
rs375720710	snp	C/T	1.71132e-05	0.00292511	missense	MYCBP2	GRCh38.p7	13:77270532	GCGAATTTAGAATTG[C/T]TGGCACCTAATCAAA	23077
rs375723459	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77231131	AGTAAAAAGATAAAA[A/C]TATCTCACTCTATAA	23077
rs375735068	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77175403	CCCATAGGAAAAAAG[A/C]TGTCCAAAATATAAT	23077
rs375742271	in-del	-/TATTG			intron-variant	MYCBP2	GRCh38.p7	13:77307663	AAAAAAACTTCATTG[-/TATTG]AAGTTTTTTAACACC	23077
rs375755477	snp	C/T	0.000155988	0.00883004	intron-variant	MYCBP2	GRCh38.p7	13:77064564	TACTAAAAAAGAACA[C/T]GCAATGATACACACC	23077
rs375759363	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77170712	CTTCTGAGTAGCTAG[A/G]ATTACAGGCACCTGC	23077
rs375772342	snp	A/G			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77084951	TTGGGCTCTTTTCCC[A/G]ATTGTGGGGCTTACC	23077
rs375783156	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77215672	TCTCACTACAGCCTC[A/G]ACCTCCAGGGCTCAA	23077
rs375789398	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77236108	GACTGGAGGTAAGGC[C/T]AGTTAAAAGGCTTTT	23077
rs375803464	in-del	-/AAC	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77293693	AAGAGGAGGAGATAA[-/AAC]AACAGAAAACTATCA	23077
rs375807007	snp	A/G	1.64988e-05	0.00287213	synonymous-codon	MYCBP2	GRCh38.p7	13:77211250	ATTAAAAGTTTTACA[A/G]CTCCCATCCACTTTA	23077
rs375819712	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77085217	AACTCATTTGGAAGC[A/G]TTACTTAATTTCCCT	23077
rs375835452	snp	A/G	0.000153988	0.00877328	intron-variant	MYCBP2	GRCh38.p7	13:77126271	CTTTGGTTGTATTAC[A/G]TTAAAAATGAGTATC	23077
rs375841107	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77136368	ACTCTTTAACTATAG[C/T]GCATTCACTATATTG	23077
rs375856607	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77170322	GTTATCCATGAACAT[G/T]GTGCTGGAAAGATAA	23077
rs375863786	snp	A/C	0.000153988	0.00877328	missense	MYCBP2	GRCh38.p7	13:77146197	AAAACGTAGTTCTTC[A/C]AATGAATAATTTTCA	23077
rs375874647	snp	A/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77319125	GTGTGTGTGTGTGTG[A/T]TTGTGTGTACAGTCC	23077
rs375885803	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77210262	CAGTGGTGCGATCTC[A/G]GCTCACTGCAAATTC	23077
rs375918443	snp	C/G	2.05539e-05	0.0032057	intron-variant	MYCBP2	GRCh38.p7	13:77278944	ATATATATACTTTAT[C/G]ACATGTAAGCTAGTA	23077
rs375923506	snp	A/T	0.000273376	0.0116882	intron-variant	MYCBP2	GRCh38.p7	13:77205638	TAACTCCTTGAAATT[A/T]AAATGTCCTATGGTA	23077
rs375938599	snp	C/T			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77078480	GAGGACAATAACCTG[C/T]ATTAACTCAAAGTAT	23077
rs375940133	snp	A/T			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77293582	AAGGGACTCTGTATA[A/T]GTGATTAAACTAAGG	23077
rs375951566	snp	A/G	8.2648e-05	0.00642784	missense	MYCBP2	GRCh38.p7	13:77058378	TGGCCACAAGGATGC[A/G]TCTTACTACAGGCTA	23077
rs375991120	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77305258	ACATAGAAGCAAAAA[C/T]ACTGCACAGCCAAAA	23077
rs375993356	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77057725	GCTGAGCATGCAACA[C/T]AGAAAGCACAGCATA	23077
rs375994555	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77220404	TAACCTGGCCAAGAT[C/T]ATATAGCTACCAAGT	23077
rs376000473	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087811	TAAGAGACAGTGTCT[C/T]GCTCTGTCACCCAGG	23077
rs376015537	snp	A/G	1.73078e-05	0.0029417	intron-variant	MYCBP2	GRCh38.p7	13:77264005	TCAGTGTGGCAATCT[A/G]TGCAAAAGAAAAAGT	23077
rs376030235	in-del	-/ACACACAT			intron-variant	MYCBP2	GRCh38.p7	13:77166969	CTTCAAAGACAAAAC[-/ACACACAT]ACACACACACACACA	23077
rs376038131	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77050876	ATCAAGGAATTCCTC[C/T]TGCTTCTTTAGGCTA	23077
rs376040303	in-del	-/T			intron-variant	MYCBP2	GRCh38.p7	13:77257530	TATCTACCCATAAAA[-/T]TTTTAAAAAAAATTT	23077
rs376054534	in-del	-/C			intron-variant	MYCBP2	GRCh38.p7	13:77177334	CAATTTCTTTTCTTT[-/C]TTTTTTTTTTTTTTT	23077
rs376080390	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77246927	TTCAATGCCCTTTCA[C/T]AATAAAAACAGTAGA	23077
rs376083823	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77056110	GTTTGGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT	23077
rs376111946	snp	A/T	6.60273e-05	0.00574537	intron-variant	MYCBP2	GRCh38.p7	13:77194260	CTAAGGAAAGGAGAA[A/T]GACAATCATTTATAT	23077
rs376118942	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77163896	TCTCTCCTCTTCACT[A/G]ACTGTTCCTTCACAG	23077
rs376141324	snp	C/T	0.0107246	0.0724382	intron-variant	MYCBP2	GRCh38.p7	13:77202497	CCATTCCTTCTGAAA[C/T]TATTCCAATCAATAG	23077
rs376144635	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77047178	TAGTGAAAACACACC[A/T]GCAAACATCTGAGTG	23077
rs376155094	snp	A/G	1.99189e-05	0.0031558	intron-variant	MYCBP2	GRCh38.p7	13:77288409	ATATTTCCATTTCAC[A/G]CTCTTTTCTATCATC	23077
rs376156645	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291510	GTGCAGTGACTCACG[C/T]CTGTAATCCCAGCAC	23077
rs376162422	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77071954	CCCAAATATTTGGGA[A/G]TTAAACAAGGTGCTT	23077
rs376191917	snp	A/G			missense	MYCBP2	GRCh38.p7	13:77156174	AAGATGTTTTCTGAG[A/G]ATCCGCATATGAATC	23077
rs376198378	snp	A/G	1.65151e-05	0.00287355	missense	MYCBP2	GRCh38.p7	13:77206697	GTAGTGAGGGCCCTT[A/G]ATCCTGTTGGTAAGG	23077
rs376204786	snp	C/T	0.000120386	0.00775747	synonymous-codon	MYCBP2	GRCh38.p7	13:77097509	CCTGGGCCTAACTTC[C/T]GCCTTTTCTTTTTTC	23077
rs376208328	snp	C/T	0.00279162	0.0372561	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77080272	GCAGACTGGCCTGCA[C/T]CCAGGTTATCTGAGA	23077
rs376208791	snp	A/G	4.96093e-05	0.00498018	intron-variant	MYCBP2	GRCh38.p7	13:77121500	AAGAGCTTGTTCTAC[A/G]ATAAAAGCCATAGCT	23077
rs376237908	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77209242	CAACCAGCTGAACAT[A/C]ATACTTGAGAGTTCT	23077
rs376252859	snp	C/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77054218	TTAAACACCAATGGC[C/T]TGTGCAATGGCATGG	23077
rs376258720	snp	A/T			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77086474	GGCTTCTTGACTCAA[A/T]GGGTTGTTATCTGTA	23077
rs376268218	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77290067	CAAATGGGCAAAAGA[C/T]AGGAATAAACACATC	23077
rs376279711	snp	A/T	1.65124e-05	0.00287331	missense	MYCBP2	GRCh38.p7	13:77165276	ATTCATTCTTACCTC[A/T]TCAGGTCCAGGGCTA	23077
rs376292784	snp	C/T	1.68653e-05	0.00290385	intron-variant	MYCBP2	GRCh38.p7	13:77051799	TTGTTTCTAATAAAA[C/T]GTTCTGCCTACCTGA	23077
rs376328232	in-del	G/TCC			intron-variant	MYCBP2	GRCh38.p7	13:77219382	AGAATACACAAAGTA[G/TCC]CTCTAAGTATCCCAG	23077
rs376387854	snp	C/T			intron-variant, utr-variant-5-prime	MYCBP2	GRCh38.p7	13:77227111	TCTTGAGCCCTTGGT[C/T]TGAAAAGCTAGTGAT	23077
rs376398832	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77053398	TCAAAAAGCTATGTC[C/T]GGATTGGGAATAAAC	23077
rs376401653	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77269984	GTTTATTGTGGATAG[C/T]TTCTTACCTGAGCAT	23077
rs376419770	snp	C/T	1.67792e-05	0.00289643	intron-variant	MYCBP2	GRCh38.p7	13:77096292	TCATTAAAAGTATAG[C/T]TCCAAATGGAATAAA	23077
rs376423689	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77278526	GAGAAGCTCTTCACT[C/T]TTTAAAAACTGCAAA	23077
rs376425526	snp	A/T	0.000153988	0.00877328	intron-variant	MYCBP2	GRCh38.p7	13:77233105	CAAAATTCAAATGAG[A/T]GGAAGAAATTGGGAA	23077
rs376439838	snp	A/G	1.66239e-05	0.00288299	intron-variant	MYCBP2	GRCh38.p7	13:77270087	AAAACAAAAGTTAGT[A/G]TATCAGTGGTTTCAT	23077
rs376446166	snp	A/G	0.000153988	0.00877328	intron-variant	MYCBP2	GRCh38.p7	13:77191830	TGAGAAAAAATTAGT[A/G]AGTCAAAAACAATAT	23077
rs376448046	snp	C/T	0.000121863	0.00780492	intron-variant	MYCBP2	GRCh38.p7	13:77099039	CATTTTACAGTGAAA[C/T]TTATTAATAAAATTA	23077
rs376456478	snp	C/T	1.88014e-05	0.003066	missense, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087515	TTGCTTGTTTTATTT[C/T]CTTCATCCTCTTCTT	23077
rs376465915	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77180756	TTTGTCTCTACAAAA[C/T]GTTTTTTTAAAAAGT	23077
rs376471324	snp	C/G	3.29527e-05	0.00405898	missense	MYCBP2	GRCh38.p7	13:77251314	CTAGTTCTTCTTCCA[C/G]GTCTTCATCCATTGC	23077
rs376484861	snp	A/G	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77258715	GGTAAGGGTGTGTGT[A/G]TATATATAAAACAGT	23077
rs376490580	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77307885	TCCTTCTACCTCTGA[C/T]GGTGGTTCCTTCTCA	23077
rs376496408	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77287236	TGTCACCCAGGCCGG[A/G]GTGCAATGGCATGAT	23077
rs376501966	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77286404	CATTTAAAAATGTCT[A/G]TATTTTCACCTATTC	23077
rs376518193	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77258379	TTTCATTATATTTGT[C/G]ATATCCAAGTGCCAC	23077
rs376529609	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77162845	TATTTTTAGTAGAGA[C/T]GGGGTTTCACTGTGT	23077
rs376535637	snp	A/G	0.000116677	0.00763708	intron-variant	MYCBP2	GRCh38.p7	13:77150716	ACTAAAATTTTTCTG[A/G]TAAGTAAAATAAATT	23077
rs376544724	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77205077	TAAATTTAAAAAATT[A/T]AGTATTACTGTATTC	23077
rs376545668	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77237917	TTGATGCGTCAAATC[A/G]AGAAAACCATAATGG	23077
rs376550357	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77204909	GTTGTGGGGTGGGGG[A/G]AGGGGGGAGGGATAG	23077
rs376550921	snp	C/T	3.34465e-05	0.00408927	missense, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77078874	CAGTTAAGAAGGTCA[C/T]TGAGGTAACTTTATT	23077
rs376572662	snp	C/T	1.65334e-05	0.00287514	missense	MYCBP2	GRCh38.p7	13:77185170	GTTGGGTAGAAAGAA[C/T]GAAAGCAGGCAGTGA	23077
rs376574018	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77123896	TATGAATATGAAGTA[A/T]ATATACAGCAATATA	23077
rs376579301	snp	A/G	8.30517e-05	0.00644352	synonymous-codon	MYCBP2	GRCh38.p7	13:77064681	GGTCAAGGCAATGAT[A/G]GTTTCTGCAATAGCA	23077
rs376586155	snp	A/T	1.64988e-05	0.00287213	missense	MYCBP2	GRCh38.p7	13:77098294	TCTTAAATTCACTGC[A/T]GTCATCGCAGGTGCT	23077
rs376621562	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77124111	CTCAATGTGTACAGC[A/G]TGGTGTAATGAGTAC	23077
rs376623733	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77110454	TTTATCAAGACAATA[C/T]GTGCACAGCTGAACA	23077
rs376632688	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77150361	TACTGAGGCTGGTCT[C/T]GAACTCTTGGCCTCA	23077
rs376640072	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77306859	AAAGACACCTATATA[G/T]ACTTCAGATGGTGGG	23077
rs376643235	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77200869	TCACCACCAGGCCTG[A/C]CCTAAAAGAGCTCCT	23077
rs376652177	snp	C/G	0.000447482	0.0149513	intron-variant	MYCBP2	GRCh38.p7	13:77177710	ATCCTGATACACAAC[C/G]CACTAATCAGGATAA	23077
rs376656285	snp	C/T	3.3195e-05	0.00407387	missense	MYCBP2	GRCh38.p7	13:77146172	CTTACCTCTTAGGAG[C/T]TGGTGATGCAAAACG	23077
rs376662062	snp	A/C/G			intron-variant	MYCBP2	GRCh38.p7	13:77106902	TCCTCCTCCCACCTT[A/C/G]GATGCAATCTTAACT	23077
rs376676410	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77254297	ATCAAAGTCATGATC[A/G]CGGTTAGCTCTGGGG	23077
rs376704124	snp	C/G/T	0.00106782	0.0230819	intron-variant	MYCBP2	GRCh38.p7	13:77211923	AATCAAGACAAGAGT[C/G/T]TGGAAGGGGCATTTG	23077
rs376705113	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77201495	TCAACAAGACAGAAA[G/T]TCAACAAGGATATCC	23077
rs376726932	in-del	-/T			intron-variant	MYCBP2	GRCh38.p7	13:77210194	AAAGCACCACAATAA[-/T]TTTTTTTTCTTTTTT	23077
rs376741378	snp	A/G/T	0.00029776	0.0121982	intron-variant	MYCBP2	GRCh38.p7	13:77058455	TGTAAAAAAGCACAC[A/G/T]TTCTGGTAATTTTCC	23077
rs376787733	snp	G/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77151379	CACTGTTCTACAGAA[G/T]AAAATGTACTCTATT	23077
rs376826068	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77247658	ACTCGGTTTTGACTT[C/T]AAAACTTACTACAAA	23077
rs376827492	snp	C/T			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77082914	GGGAGGCACCATCTA[C/T]ATAATGTAGGGATTC	23077
rs376829233	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77148656	TGATTGTTTTATCCA[G/T]GCTCATATGACTCAC	23077
rs376835651	snp	C/T	0.000153988	0.00877328	intron-variant	MYCBP2	GRCh38.p7	13:77062549	AGCTAAGCTAAAGCT[C/T]ACTGTAAAGGAAAGC	23077
rs376836697	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77295456	ATTTCATCCCCGGAT[A/C]CATCTGTGTCTCAAG	23077
rs376867730	snp	A/G	3.60036e-05	0.0042427	intron-variant	MYCBP2	GRCh38.p7	13:77169570	CTTTTTTTAAAAAAG[A/G]TATTTAAAAAAAACA	23077
rs376873859	in-del	-/TA			intron-variant	MYCBP2	GRCh38.p7	13:77275179	TCCAGGGAAAGAAAA[-/TA]GTCAATAGTTTAAAC	23077
rs376901350	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77130145	TCTAGTGAGTAGCAA[C/T]TGCACAATTTTATTG	23077
rs376931021	snp	A/G	6.76155e-05	0.00581405	missense	MYCBP2	GRCh38.p7	13:77270519	ACACTTCTCTGTAGC[A/G]AATTTAGAATTGTTG	23077
rs376940997	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77216767	AAAGGAGACTAAAGA[C/T]ACACAACAGGCAAAT	23077
rs376951416	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77139587	AACACAAGGAAACCA[C/T]ACTTTAAGATACATA	23077
rs376958432	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77252682	CAGGTCTATCTAACC[A/C]AGAAATAAACTCATA	23077
rs376967825	snp	C/T	1.65359e-05	0.00287536	intron-variant, nc-transcript-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076860	AATACCTGATGAAGA[C/T]ATGCATGTGAGAAGG	23077
rs376980736	snp	A/G	0.00110542	0.0234838	synonymous-codon, utr-variant-5-prime	MYCBP2	GRCh38.p7	13:77225535	GCTTGCATCCTTTTC[A/G]CCTCTTTCTCCACTT	23077
rs376981551	snp	A/G	0.000102189	0.00714729	intron-variant, nc-transcript-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087647	GCCTGAAGAAATGAC[A/G]GTTAAATGAGTTCAA	23077
rs376996843	snp	A/C	1.64893e-05	0.0028713	missense	MYCBP2	GRCh38.p7	13:77065997	GGGAACTTACTGCTG[A/C]CATATCCTTGATAAG	23077
rs376997274	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77318582	AATATGGTGAAACCC[C/T]ACCTCTAGTAAAAAT	23077
rs377007998	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77192170	CTCATTCATTCAGCT[A/G]AATAGTTTTGAAAGG	23077
rs377013710	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77119825	AAACTCCTGGCCTCA[A/G]GTGATCCTGTTGCCT	23077
rs377034695	snp	C/T			intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77325655	TATTCTGAAGTTCTG[C/T]AGTTTTCCCCTTTTC	23077
rs377042669	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77209683	TGTTATTTCATCTAC[C/G]CTGCACAATGCTGCC	23077
rs377054820	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77106474	ATTCAGGAGGCTAGG[C/T]GTCTAATCACAATGC	23077
rs377071981	snp	A/G	1.66217e-05	0.0028828	intron-variant	MYCBP2	GRCh38.p7	13:77177964	ATCAACCTGTGAACA[A/G]TAAAAGCAATTGTAT	23077
rs377079165	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77129485	AAATTAAGAGCCAGA[C/T]GTTGTTATAAAGCTT	23077
rs377106679	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77155459	TCAGAAATAAAAGTT[A/T]TAAATGAGATATTCA	23077
rs377110074	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77053133	ATATGGTGAGACCCC[A/G]TCTCAAAAAAAAAAA	23077
rs377113806	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77107445	CATAGGATTTTTCAG[A/G]AAGTGACAGGACTAG	23077
rs377115366	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77128663	TAAAGTCATAGAACT[A/G]TGCCTATCATGCTCA	23077
rs377129003	snp	A/C/G	9.97165e-05	0.00706041	intron-variant	MYCBP2	GRCh38.p7	13:77140989	TGAGAAAAAAAGAGA[A/C/G]GGAAGATCCTTAAAC	23077
rs377145676	snp	C/T	3.29734e-05	0.00406025	missense, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081450	CTCGGGAATTGTCCA[C/T]GTGAACAGACACATA	23077
rs377163127	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77099233	AACTATTTTCATGGA[C/T]GCAAAACAACAGGTT	23077
rs377177103	snp	C/G	0.000116567	0.00763346	synonymous-codon	MYCBP2	GRCh38.p7	13:77185914	GACACGCAATAACCT[C/G]AGACAACAGGTACCC	23077
rs377179218	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77203229	AATGTACAAAAATCA[C/T]AAGCATTCTTATACA	23077
rs377179330	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77124585	TTTCAGTACTAGGAA[G/T]GGAAAGATAAAAACC	23077
rs377188860	snp	C/G/T	4.95334e-05	0.00497641	synonymous-codon	MYCBP2	GRCh38.p7	13:77180145	AGATCCCAGGGCTGA[C/G/T]GCTGTCAGTTCACTG	23077
rs377190370	snp	A/T	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77048173	GGGTGGAATCCATGA[A/T]TGGGATTAGTGCTCT	23077
rs377222674	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77158539	CCTCAACCTCCTGGG[A/C]TCAAGCGATCCTTCT	23077
rs377226293	snp	C/T			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77292656	TAGGGAGGGATGGAA[C/T]CAGCAGAGGGTAAGA	23077
rs377242753	in-del	-/AACT			intron-variant	MYCBP2	GRCh38.p7	13:77288463	AAGATTAGACACACT[-/AACT]GACTTGCAGAAGACA	23077
rs377254574	snp	A/G	0.000315209	0.0125501	intron-variant	MYCBP2	GRCh38.p7	13:77264009	TGTGGCAATCTGTGC[A/G]AAAGAAAAAGTATTT	23077
rs377261717	snp	C/T	1.65061e-05	0.00287277	missense	MYCBP2	GRCh38.p7	13:77185990	AATCCTTTTAATCCT[C/T]TAAGTTCTTCAACTC	23077
rs377267671	snp	C/T	0.000115671	0.00760408	synonymous-codon	MYCBP2	GRCh38.p7	13:77098457	TACTGATTTTGGTTT[C/T]GGTGACGTTGACCGT	23077
rs377269565	snp	C/T	1.75745e-05	0.00296428	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081681	TATAAGTACTTATGA[C/T]ACTTAAAAGCAAATC	23077
rs377274684	snp	A/G	4.96504e-05	0.00498224	utr-variant-3-prime	MYCBP2	GRCh38.p7	13:77045373	AGACAAAGGATCTGC[A/G]TGTTCTAAAAAGTGT	23077
rs377280278	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77281428	GATATTTAATAAAAA[A/T]AATAATTATAACAAT	23077
rs377284467	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77229760	TGTAGTTCTAGTAAA[C/T]GACAAATTCAGAAAT	23077
rs377286511	snp	G/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77197246	GAGAGAATGGAGACA[G/T]AAAGTATAGAAAGAA	23077
rs377308267	snp	A/G	1.71202e-05	0.00292572	intron-variant	MYCBP2	GRCh38.p7	13:77261150	ATTTTTATTAAATGC[A/G]TAGTTGATCACTCAA	23077
rs377308547	snp	C/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77284386	CAGAGAAGGTCAAAG[C/G]GAAAAGAAAAATGCC	23077
rs377310506	snp	C/G/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77199028	TAGTATTACTGTAGG[C/G/T]GGGGAGGAGGCAAGA	23077
rs377311458	snp	A/G	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77244667	AAAATTGACAAATGG[A/G]ATCTAATTAAACTAA	23077
rs377315425	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77182988	AACTGCTAGTTTCAT[C/T]AACCACTGTTCCTGT	23077
rs377363501	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087846	AGTACAGTGGTGTGA[C/T]CATGGCTCACTGCAG	23077
rs377372455	snp	A/C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77248826	ACTCATCTTCACAGC[A/C/G]CATTACTCACAATAG	23077
rs377373008	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77125879	ACTACATCTTCAAGC[A/T]TATCAGCTGAGGCAA	23077
rs377376035	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77134593	ATAACAAAAAAAAAA[-/A]GGAAAAGTGTTCTAA	23077
rs377379998	snp	A/G	9.91015e-05	0.00703853	missense	MYCBP2	GRCh38.p7	13:77067819	TGATGCTGGCCAGAC[A/G]ACTAGGGGTTACTTC	23077
rs377383858	snp	A/G	8.23635e-05	0.00641677	intron-variant	MYCBP2	GRCh38.p7	13:77140821	AAATTGAATGATTCC[A/G]GCTCTCAATTCATTC	23077
rs377389935	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77100250	TGTTTTTTATGCTTC[C/T]GTGCATGTGTTAAGT	23077
rs377390731	snp	A/G	0.000153988	0.00877328	synonymous-codon	MYCBP2	GRCh38.p7	13:77067708	TGGCAATGCATCCTA[A/G]AAACATGTCCAAGAT	23077
rs377421523	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77092911	TCCCTACTCTGATTT[A/G]CTACAGCATTAAGTA	23077
rs377430340	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77113117	TGATTCATTGGATCT[C/T]TGTAATGTAACTCAT	23077
rs377452207	snp	C/T	5.3294e-05	0.0051618	intron-variant	MYCBP2	GRCh38.p7	13:77211128	AAGAGTATAACTGCA[C/T]CAAAACTTATTGACT	23077
rs377479834	snp	A/T			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77294080	ATAGAGGGGTTGATG[A/T]TAGCCATAAAGTAGA	23077
rs377480303	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77065502	AATGACAAGGAGCAA[C/T]TAATCAGAGCCAGGC	23077
rs377487912	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77173314	GCTCTCCAGCTTTCT[A/G]AAACACGTAACTCTT	23077
rs377516675	snp	A/G	1.66078e-05	0.00288161	intron-variant	MYCBP2	GRCh38.p7	13:77174291	TAAAGTATTTCCGTT[A/G]TCTCTATACATTCAC	23077
rs377540606	snp	C/T			intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77325948	AAAACTCAACCAATC[C/T]ATACCATGACTCCTC	23077
rs377552284	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77298315	CTTAAGTCTAACTCC[A/C]CACACTGGATGAGTT	23077
rs377553580	snp	C/T	3.78329e-05	0.00434914	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076732	GGGAAATAAATATCT[C/T]TAGAATACAAATAAA	23077
rs377559701	snp	C/T	1.69017e-05	0.00290699	missense	MYCBP2	GRCh38.p7	13:77211177	CTTACCTCCAAATTA[C/T]ATCATATACAGGATC	23077
rs377565885	snp	C/G	4.95954e-05	0.00497948	missense	MYCBP2	GRCh38.p7	13:77260484	AGTTCTCCATCTTTA[C/G]AAATAACAGAACTAC	23077
rs377565904	snp	G/T	8.23676e-05	0.00641693	missense	MYCBP2	GRCh38.p7	13:77125401	CATGCCTCTCCTTCA[G/T]CACTCTCACAGAACT	23077
rs377584025	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77239028	GGGAGGCCGAGGCAG[A/G]AGAATCGCTTGAAAC	23077
rs377597588	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77170343	GGAAAGATAAGCTGA[A/G]CCTATACTGTGAAGA	23077
rs377600565	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77145787	ACAATCAAATACAAG[G/T]ATACCACATGCTGAA	23077
rs377603176	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77213938	CCGGCTACTGCAAAC[C/G]TGAGCATGTGCAAAG	23077
rs377606008	in-del	-/TTTA			intron-variant	MYCBP2	GRCh38.p7	13:77112326	TTTTATATATAATGT[-/TTTA]TTTATATAATATATA	23077
rs377626874	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77270798	CAAGTACTCTATCTC[C/T]ACAAATCTATTATTG	23077
rs377655525	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77297649	TTAGAAGGAAGAGTT[A/G]GCCTGCTGGAAAAAA	23077
rs377717882	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77304528	GGAGTAAGTTTGAGT[A/G]TTATATAGCACCACA	23077
rs377762522	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77151454	CCTAAAGCCCAAATA[C/T]GTTTCTTTACTCGGG	23077
rs386352333	snp	A/G			missense	MYCBP2	GRCh38.p7	13:77051078	TTCTGTTTTGGAACA[A/G]CACATTTTTGTAATG	23077
rs386379836	in-del	-/T			intron-variant	MYCBP2	GRCh38.p7	13:77299011	TATTCTTCATACTAT[-/T]TTAGGAAACCAACTT	23077
rs386772501	multinucleotide-polymorphism	CGC/TGT			intron-variant	MYCBP2	GRCh38.p7	13:77048681	ATAATACCATCTACT[CGC/TGT]AGATTGTAAAAATGG	23077
rs386772502	multinucleotide-polymorphism	AT/GC			intron-variant	MYCBP2	GRCh38.p7	13:77104397	AGGAACAAAGTCCCT[AT/GC]TCTCACAGAGTTTAT	23077
rs386772503	multinucleotide-polymorphism	CT/TC			intron-variant	MYCBP2	GRCh38.p7	13:77142906	CAAAATCAGAAAAAG[CT/TC]CAAAATCTAGAATAC	23077
rs386772504	in-del	AAA/C			intron-variant	MYCBP2	GRCh38.p7	13:77223915	CTAAAACTAAAACTA[AAA/C]CAAATGAAGTAGGGA	23077
rs397697122	in-del	-/T	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77153762	TAAACTTTTTTTTTT[-/T]AATTCACAGGAAGTT	23077
rs397707421	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77072325	AAAAAAAGAAATCAA[-/A]ATGGGAATAAGAAAA	23077
rs397712661	in-del	-/A	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77243981	AAAAAAAAAAAAAAA[-/A]GACAACTGAGATATT	23077
rs397715625	in-del	-/AC	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77131541	CACACACACACACAC[-/AC]TTGAATAGTGTTCTT	23077
rs397730940	in-del	-/A	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77092095	GAAAAAAAAAAAAAA[-/A]CCTCATTTGGATATA	23077
rs397775603	in-del	-/A			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77292539	AGATTTAAAAAAAAA[-/A]AGAGCACTCACAATA	23077
rs397775939	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77072326	AAAAAAGAAATCAAA[-/A]TGGGAATAAGAAAAC	23077
rs397782661	in-del	-/AAG			intron-variant	MYCBP2	GRCh38.p7	13:77222411	TGTGTTTTTAATAAG[-/AAG]TTCAACTCAATGATA	23077
rs397795046	in-del	-/A	0	0	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77292540	GATTTAAAAAAAAAA[-/A]GAGCACTCACAATAT	23077
rs397814778	in-del	-/T			intron-variant	MYCBP2	GRCh38.p7	13:77176033	CTTTTTTTTTTTTTT[-/T]AAATGAGTTAGGGCA	23077
rs397832830	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77056103	ACGCTCTGTGTTTGg[G/T]gtgtgtgtgtgtgtg	23077
rs397840781	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77166323	CAGAAGAAAAAAAAA[-/A]CTTACCTGGCAACAC	23077
rs397841264	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77048864	ACTGAGTTCTCTAAA[-/A]GTGTTTCATTGTTAA	23077
rs397841691	in-del	-/AT			intron-variant	MYCBP2	GRCh38.p7	13:77068976	TTAATTCTCCATCAT[-/AT]GTCATTCTCTTAACT	23077
rs397851660	in-del	-/T			intron-variant	MYCBP2	GRCh38.p7	13:77276817	ATTTCCATGCCCAGT[-/T]TTTTTTTTTTTTTTT	23077
rs397851931	in-del	-/T			intron-variant	MYCBP2	GRCh38.p7	13:77176020	ACAAAACAAAAACAC[-/T]TTTTTTTTTTTTTAA	23077
rs397944571	in-del	-/A			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77080956	GAAAAAAAAAAAAAA[-/A]GCTGATTACACTATA	23077
rs398023530	in-del	-/GA	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77233897	AGAGAGAGAGAGAGA[-/GA]AAGGAGCTTGGGCTT	23077
rs398023532	in-del	-/T	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77276839	TTTTTTTTTTTTTTT[-/T]GGAGAGATAGGGGTC	23077
rs398023536	in-del	-/AC	0	0	intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326283	CACACACACACACAC[-/AC]GAGAAACTGCAGCCA	23077
rs398023537	in-del	-/A	0	0	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77328177	TTCTCTTAAAAAAAA[-/A]TAAAATAAATGTTAA	23077
rs398037679	in-del	-/C	0.5	0	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77074012	CCACCGCCCCCCCCC[-/C]TTTTTTTTTTAAAGA	23077
rs398077406	in-del	-/T			intron-variant	MYCBP2	GRCh38.p7	13:77111596	TAATTTTTTTTTTTT[-/T]TCTTTTAAGTAGAGA	23077
rs398117586	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77195600	ACTCTTAAAAAAAAA[-/A]TAGTCCGAAATAATC	23077
rs398117587	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77261396	TATTAAAAAAAAAAA[-/A]GGAATTATGGTACTT	23077
rs398117588	in-del	-/AC			intron-variant	MYCBP2	GRCh38.p7	13:77310803	CACACACACACACAC[-/AC]CATATTTAGGTACAA	23077
rs398117589	in-del	-/T			intron-variant	MYCBP2	GRCh38.p7	13:77316962	TGTTGTTTTTTTTTT[-/T]GTTTTGAGATGGAGT	23077
rs527241831	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77218049	ACAAGGAGTAGGAAA[C/G]ATAAAAGGCACTCAT	23077
rs527276691	snp	G/T	1.65293e-05	0.00287479	missense, intron-variant	MYCBP2	GRCh38.p7	13:77126465	CAAGAATGGCATATC[G/T]TGTTCTTGCATTGTT	23077
rs527301793	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77179544	AAACTTTGTGATAAT[A/G]TACAACTAAGTACAA	23077
rs527303592	snp	A/G	6.61474e-05	0.00575059	missense, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77077369	TTACCCAGCCAATGT[A/G]CCTGGAATCCAGATC	23077
rs527312265	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77272487	ATATGGTATCTGAAT[A/G]TTTGTGTTACTTTAT	23077
rs527322526	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77235718	TAATGAGGGGAGGGA[G/T]GGTTTACACACAACT	23077
rs527339164	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77265962	CTTCACCACTAATAC[A/T]GCACACACTTATGAA	23077
rs527343591	snp	C/T	4.95282e-05	0.00497611	intron-variant	MYCBP2	GRCh38.p7	13:77225429	CCCTAAAGTTCCAGC[C/T]GCTACCTGAATGGTG	23077
rs527351664	in-del	-/T			upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77328425	ATTAGCCCTGTTAAG[-/T]TTTTGTATTTGTCTT	23077
rs527367393	snp	A/T	1.66067e-05	0.00288151	synonymous-codon	MYCBP2	GRCh38.p7	13:77061764	GATTGCTGCAGTTTC[A/T]CCATCATCATGGTTA	23077
rs527375508	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77120051	ATGACTGATTTACTG[G/T]GATAGCTATTAGTAC	23077
rs527380148	snp	A/G			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77085972	GTCCTATTTTTCCTT[A/G]CAGTCTGTCAATTGT	23077
rs527384335	snp	C/T	0.00478085	0.0486577	intron-variant	MYCBP2	GRCh38.p7	13:77205673	TGACATTAAATGCTA[C/T]AGGGGATAAATTAAA	23077
rs527402546	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77117918	ATAAAAATAAAGACA[A/G]GAAACAACAATTTGA	23077
rs527405285	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77218806	GAAACACAACCATTA[C/T]AGAAATAGTCCACAC	23077
rs527408726	snp	C/G/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77169163	CCTGTAATCCCAGCA[C/G/T]TTTGGGAGGGCGAGG	23077
rs527418830	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77152988	GAGAATGGAGTGAAC[C/T]CAGGAAGCGGAGCTT	23077
rs527420537	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77317893	AGTCAGCTGAGATCA[C/T]GCCATTGCACTCCAG	23077
rs527423616	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77273146	CATGAATGAATTCCA[C/T]ACTAAAAAACTCAGG	23077
rs527425113	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77171170	TAGCGATACATTACT[A/G]GAAAAAGAACAGAGA	23077
rs527430326	snp	A/G	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77069868	GCGAGACTCCCTCTC[A/G]AAAAAAAAAAAAGTT	23077
rs527431251	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77311307	AGAATTATAATAAAC[A/C]CTAGAGTTTACAAAA	23077
rs527436905	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77163656	CCTCATCTCTGTTCT[A/G]CTTCAATGAAAAATT	23077
rs527455428	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77054804	TGGGGTTTTGCCATC[C/T]TGCCCTGGGTGGTCT	23077
rs527463558	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77150170	GAGCTAAAAATCCCA[A/C]AGAGTTCTAGGAGAT	23077
rs527479972	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77324310	TCTCACACCTTTAAA[C/T]CTGATGCTCACTAGA	23077
rs527485895	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77110739	CTCTTTTTTTCTCAG[A/C]CTGGCCAATGCTTAG	23077
rs527495723	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77318556	GTGAGGAGTTCGAGA[C/G]CAGCCTGACCAATAT	23077
rs527495923	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77047836	AGCTGAGTCACGCTG[C/T]GGGCCAAGACAGCCC	23077
rs527502083	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77177011	CCCATTTTAATAAAA[C/G]TCAGGTACTTTAATT	23077
rs527508322	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77310618	ATCATATATATATAA[C/T]TGGATTCCCAGAAGG	23077
rs527510417	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77258229	ACTTGCCATAGTATA[C/T]TGACATGAAATTGTT	23077
rs527511003	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77249243	CCACAGAACTGTCTA[C/T]TTAAAAATGGTTAAG	23077
rs527514416	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77164818	GTATGATTTAAAACA[C/T]TTAGACAAGATGATA	23077
rs527519850	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77211391	CCAAAACCCATAAAG[C/T]AGTATTATCTCCATT	23077
rs527552190	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77095086	GAAGTCAGCCTACCA[A/C]AGAGTAAAAGATAGC	23077
rs527559599	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77086759	TTAGATTAATTTTTA[C/T]GTATTTTCTTTAGTT	23077
rs527578110	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77151267	ATCTACATTAAGTTA[C/T]TGCAGGGACTAACAA	23077
rs527588187	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77143242	TTTGCGTCTGTGAGG[A/G]TGTTTCCAGACAAGA	23077
rs527595202	snp	A/G	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77203972	AGGCATTACCATTCA[A/G]GACATAGGCATGGGC	23077
rs527596819	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77299429	TAATTATAAATTACT[C/T]TTACTGTGTTTTTTG	23077
rs527612562	snp	C/T	0.000798403	0.0199641	intron-variant, missense	MYCBP2	GRCh38.p7	13:77103298	CGAGAAGCAAGGTTG[C/T]GAGATGGAGATTCTA	23077
rs527619569	snp	A/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77250697	TTTAGAAGCAAGCAT[A/T]CAACGTTTCTAAATT	23077
rs527652295	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77124573	GTGTCAAAACTGTTT[C/T]AGTACTAGGAATGGA	23077
rs527654066	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77236554	CTACAACTTTATTCA[C/T]TATAGCAACATTTTA	23077
rs527669243	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77197647	TAGGGCTGGGTCTTT[A/G]AGGAACTCCTACATT	23077
rs527671399	snp	A/G	3.29549e-05	0.00405911	synonymous-codon, utr-variant-5-prime	MYCBP2	GRCh38.p7	13:77288245	AGAGTTCTTAGATGC[A/G]GCTGCCAATGATATT	23077
rs527690271	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087405	CTGCGAATGATTTCA[A/T]GCAAATTATTGGACT	23077
rs527693820	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77155681	TCAGTAATACCAAAC[A/G]CAGAACGTACTTGAG	23077
rs527736796	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77181229	AGCTGATTTCCAGCA[G/T]GAAAATGATTTATGT	23077
rs527756518	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77088010	GCTGGTCTCAAACTC[G/T]TGCGCTCAAGTGATC	23077
rs527765873	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77237340	ACATATGTCTACACT[G/T]TCACATATGTGTAAG	23077
rs527794046	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77136923	CATCTATATCTTTAA[C/T]TTCTCCCTTTTTCTA	23077
rs527824944	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77078681	TCCTATGTTTTGGAC[C/T]ACTTGTCAATTTAGT	23077
rs527834251	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77183753	GACTGAGTTTTGCCA[A/T]GTTAGGCTGGTCTCG	23077
rs527845961	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77220685	TGTTGTAGTTAATAC[A/G]TATGCTATAGAAGCT	23077
rs527880362	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77327585	TTACTTACAAAGACA[A/G]GTAGTAATCTAGCAC	23077
rs527905895	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77172794	ACTAGCCAACTATAA[C/T]GAACATCCTTAAAGA	23077
rs527908248	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77210434	CCTGACCTCGTGATC[C/T]GCCCGCCTTGGCCTC	23077
rs527932345	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228870	GTTCAGTATCTAAGG[A/G]ACTCTAACTTCTAAT	23077
rs527937627	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77119172	CTAAAATATCGATTC[C/T]AACATTTTTCCTTGT	23077
rs527939417	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77128988	CACTTAAACTAATAA[C/T]ACATTCTTTTTGGCA	23077
rs527940008	snp	A/T	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77112344	ATTTATATAATATAT[A/T]TTTTATATATAATAT	23077
rs527968760	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77064859	AGACCATGGAATTTT[A/C]GATTATGGGCACAAA	23077
rs527971065	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77158902	CCTGCCTAAGCCTTA[C/G]TAAAGTTAAGAAGAA	23077
rs527974574	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77055427	AAACATTGGGAAACA[C/T]TGTACCAAGCTATCT	23077
rs527988574	snp	C/T	0.00478085	0.0486577	intron-variant	MYCBP2	GRCh38.p7	13:77268364	TGCTATAATAATATA[C/T]TTTCCACGGCATTAT	23077
rs527997234	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77052031	AGAAAATACCATTAT[C/T]TACTAGACCATCCCT	23077
rs527997349	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77221344	CACTGGTATAATCAG[C/G]ACCACGAAGTAATGT	23077
rs528007001	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77312442	AACTATAACATAAAG[G/T]TCTCTGGGGGAGGGG	23077
rs528008253	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77320296	TGTGCCTGAAAGCGG[A/G]ATCTGAAAGCCTAAC	23077
rs528010118	snp	A/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77173468	GCAGCAACAATGAAC[A/T]ACATAGCTATTTGCT	23077
rs528010814	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77111580	GCCCTCAATGCTTGG[C/T]TAATTTTTTTTTTTT	23077
rs528014452	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77120743	TAACTATTGTTTGGA[C/T]AGTCCATGATGCTGG	23077
rs528031046	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77165878	CTGGTTAACTGGTTA[A/G]GAATGCAACAAACCA	23077
rs528045176	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77139751	TTTCAAAACAAACAA[A/C]ATTTTAAAATGTCAT	23077
rs528047740	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77140650	GCAGGAAGAATACAA[C/T]ATGTACCAAATAAAG	23077
rs528056224	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77192679	TAGAAGAGTAGTGGT[A/G]GAAAGTCAAAAAAGA	23077
rs528056977	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77247714	GTGGCATAAAGACAG[C/T]CATACAGACCAATGG	23077
rs528070764	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77091365	CAGACATTTGTTCTG[C/T]TTTCAGAGGAAGTTT	23077
rs528076096	in-del	-/A	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77240549	GGAGGGAGAGGTTGC[-/A]GTGGGCCAAGATTGT	23077
rs528077914	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291624	AATACAAAATTAGCC[A/G]GGCGTGGCGGTGCAT	23077
rs528110964	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77146669	ATCTGAAAGGTCAAT[A/G]AAGACTAGAAAAGTT	23077
rs528112751	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77321649	AATTCCTACTGTTAC[C/T]TACATACAAACTGTG	23077
rs528160449	snp	A/G	1.65053e-05	0.0028727	synonymous-codon, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77083154	CCCGGCAATCACTAT[A/G]TCTGAGAGTGGATGT	23077
rs528171289	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77066413	GAATATAAATTCACT[G/T]TATCACTAAGCACAC	23077
rs528201983	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77131377	TTAAAAATATAGCTC[A/G]GCATGGTAGTACATG	23077
rs528208865	snp	C/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77070939	TATATTCTCCTTTCA[C/T]AAATTTCTTTAATGT	23077
rs528238650	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77196775	ACCTCCAAAATGCCT[A/C]TCAGAGAGTCACGTG	23077
rs528263093	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77323028	CCCCTCATTCTCAGC[A/G]AAAACAAACAGACAA	23077
rs528280575	snp	C/T			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77227515	ACACACACACACACA[C/T]ACAAATACATATCTT	23077
rs528315435	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77223408	ATGTATCTAATAAAT[A/T]CTTTGCATATCTAAT	23077
rs528317225	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77255652	AGTAATCCATTTCTT[C/T]TCTTTCTTTTGTTCC	23077
rs528323655	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77233101	GAGACAAAATTCAAA[C/T]GAGTGGAAGAAATTG	23077
rs528343076	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77263582	CTGGTGAAAACACAA[C/T]GTTCATTTTTAAGAG	23077
rs528345803	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77271332	AGTCAAGAGTTCAAC[C/T]CTCCAGAAAGGATTT	23077
rs528369908	snp	A/G	1.80647e-05	0.00300533	intron-variant	MYCBP2	GRCh38.p7	13:77169569	TCTTTTTTTAAAAAA[A/G]ATATTTAAAAAAAAC	23077
rs528376513	snp	A/T	1.66721e-05	0.00288717	intron-variant	MYCBP2	GRCh38.p7	13:77161979	TAAATAAAGAGTTTT[A/T]CTAAAATATGTCAAT	23077
rs528377993	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77298919	CAACTGTGTACTTTC[A/C]GCACCTGCATCAATG	23077
rs528397272	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77115259	AATGAAAATAAGGAA[G/T]GTAATATTCTTAAAG	23077
rs528401105	snp	A/G	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77271162	CACATTCTATATCAA[A/G]TAATTTCAATATCTA	23077
rs528407232	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77070573	ACAGACAAACAAACA[A/C]ACACACACACACACA	23077
rs528409310	snp	C/T	1.65326e-05	0.00287507	missense	MYCBP2	GRCh38.p7	13:77224511	CCAAATGTATAGACA[C/T]CTCCATTTTCCATTA	23077
rs528416515	snp	C/T	3.35728e-05	0.00409698	intron-variant	MYCBP2	GRCh38.p7	13:77067552	TCACTCTATTCTGTT[C/T]TGGTACTAAAATAGA	23077
rs528420832	snp	C/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77169167	TAATCCCAGCACTTT[C/G]GGAGGGCGAGGCGGG	23077
rs528429046	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77309245	GTTGGCTCATTATAA[A/T]TTCTTATTGCCAACC	23077
rs528439317	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77200964	TAAAGACCATCGAGA[A/C]TAGGAAGAAACTGCA	23077
rs528452101	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77201901	TCAAAGCAGTGTGTA[C/G]AGGGAAATTTATAGC	23077
rs528460134	in-del	-/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77189155	AATTATATATTTAAA[-/T]TTTTTTTGCCAGGTA	23077
rs528478781	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77108809	CCCAGGTTTACACCA[C/T]TCTCCCGCCTCAGCT	23077
rs528486593	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77235408	GGATTTTATAAAAGC[A/G]TAAAGATATTAAACA	23077
rs528490197	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77264076	TTACTCCTCTGTTGA[A/G]GTCAAAATGAGAGTT	23077
rs528497370	snp	G/T	8.42339e-05	0.00648921	utr-variant-3-prime	MYCBP2	GRCh38.p7	13:77045349	GATGAAGGCAATTTT[G/T]CTCTCTGTAGACAAA	23077
rs528500806	snp	A/C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77216819	GAGGGGAAAGAAATG[A/C/T]CAAAAAATAATTATT	23077
rs528502021	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77051695	TACAACACTGAACAA[A/G]TATCAGAAAATACTG	23077
rs528509657	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77059406	TGATGCTTCACATAG[C/G]TAATACACTCATTTA	23077
rs528521031	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77214401	ATAAACATGAGAAAC[C/T]GAATGAATAAACTAT	23077
rs528530572	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77093009	CCATCAAGGACCTTA[C/T]CTTAGTCATACATGT	23077
rs528531754	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77262593	GCTTGGAACAATGCC[A/T]TGCAGATATTTGAAT	23077
rs528531891	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77310106	ACGGAGTGAGACTCC[A/G]TCTCAGAAAAACAGA	23077
rs528550118	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77194906	AAACAAATGGCTCTT[A/C]AAAAAGAGGGGAAGA	23077
rs528557282	snp	C/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77201749	GAATCTCACTCAAAA[C/G]CACTCAACTACATGG	23077
rs528560038	snp	A/T			downstream-variant-500B	MYCBP2	GRCh38.p7	13:77044364	GACCCTGTCTCATAA[A/T]TAAATAAATAAAGTT	23077
rs528571384	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77148779	ATAACAATTTCATTT[C/T]ATCCGCTTTGTTTCA	23077
rs528573572	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77301920	TAAGAACTTCTCATA[C/T]GATTTTAAAAGCAGA	23077
rs528573586	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77293523	CCAAAAACTTCTATA[C/T]CCTAATTCCCCAGAA	23077
rs528576606	snp	A/G	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77066524	TGCATATTGTCATGG[A/G]TTGGCTCTACAAGTA	23077
rs528579257	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77257347	GGTGGCTACAGTTGG[C/T]GATAATTTTTTGTAT	23077
rs528585031	snp	A/C	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77200785	GAATTTCATATCCAG[A/C]CAAACTAAGCTTCAT	23077
rs528594079	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77100277	AAGTGTGTATAGTCA[C/T]GCTCTATTTCTCTAT	23077
rs528605258	snp	A/G	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77046276	GGCTTACTTTGTCAG[A/G]AAAACACGCTAGGCT	23077
rs528634273	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77301289	GGTATGGTGGTGCAC[A/G]CCTGCAATCCCAGCA	23077
rs528636600	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77133546	AGAGGTACATAAACA[C/T]AAATGGGCTGAAGGC	23077
rs528659997	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77142334	CAGAACCAAAAAACA[C/T]TTGCTGAACTAAAGG	23077
rs528660431	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77294672	CATAGCACCAAAAAG[C/T]TGAAAAGGGATAGAG	23077
rs528664924	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77093557	ATTGAACTCAGTTTC[A/T]TTCCTTTTGAGAACT	23077
rs528664947	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77241000	ATATATTTAGGACTG[A/C]AGATGAAACCTATTT	23077
rs528666784	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77249678	GGGATTACAGACATG[G/T]GCCACTACACCCAGC	23077
rs528669740	snp	C/G/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291144	AATGCAGATATCTGA[C/G/T]AAAAGACTTGTATTT	23077
rs528677729	snp	A/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77186138	CAAATGGAAAGGCAA[A/T]GGTAGACAACTTCAA	23077
rs528680914	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77259847	AGAAAATCTAGTAAC[C/T]AAATATGACAAGTTT	23077
rs528715743	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77149600	GATCACTCAGGTCTG[C/T]ACATCTAACTTTGTT	23077
rs528726715	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77320576	AGCATTAGGTAAAAG[C/G]CATTCACAATGTGCT	23077
rs528740455	in-del	-/A	0.0133709	0.080664	intron-variant	MYCBP2	GRCh38.p7	13:77261386	TATATCTTATGTATT[-/A]AAAAAAAAAAGGAAT	23077
rs528746444	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77287326	AGTAGCTGGGATTAT[A/G]GGCGACTGCCACAAT	23077
rs528759380	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77045971	TTACTGATGAAAAAG[C/T]CCACACTGGTAAAAT	23077
rs528822921	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076125	AAAAGTAAAGCAACT[A/G]TATTTTTGCAAGAAA	23077
rs528833298	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77286959	GCGCCATCTCGGCTC[A/G]CTGCAAGCTCCGCCT	23077
rs528839001	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77186958	CTGGGACTACAAGTG[C/T]GCACCACCATACCCA	23077
rs528849259	snp	A/G	1.65176e-05	0.00287376	missense, intron-variant	MYCBP2	GRCh38.p7	13:77233258	GACCAGCAAATACAA[A/G]GGGGCCTGAGGAGAA	23077
rs528867173	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77184802	CGGGGGCCTCCTGGT[A/G]CTATCCCTGCTCTCC	23077
rs528867576	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77194560	GTGAGAGAACTCCAA[C/G]AAAAAATTTTAACTA	23077
rs528895941	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77083377	TTTAGGGAAAAAAGC[C/T]GTAAGTTTAGTCACA	23077
rs528908833	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77140424	AAATACTGAAGATAC[A/G]TGTTAAGAAGGATAA	23077
rs528915580	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77177606	AGATTACAGGTGTGA[A/G]CCACTGTGGCCAGTC	23077
rs528928215	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77248680	GGAATGTAAAATGGT[C/T]GGCCGCTGTGAAAAA	23077
rs528939789	snp	A/C	0.000399281	0.0141238	missense, utr-variant-5-prime	MYCBP2	GRCh38.p7	13:77278834	CAGGGCTTGGAGACT[A/C]CTGAGACACAGGGAT	23077
rs528941288	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77239804	AGCACCTGAAAGAGA[A/G]TCCTCCATCCAATTA	23077
rs528952456	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77112660	TCTTGGCTGGTCTCA[A/G]ACTCCTGGCCTCAAG	23077
rs528961156	snp	A/G	6.58924e-05	0.0057395	missense	MYCBP2	GRCh38.p7	13:77067764	TCTGTTGAGTGAATG[A/G]TATCACTGATATCTG	23077
rs528975619	in-del	-/T	0.0123036	0.0774623	intron-variant	MYCBP2	GRCh38.p7	13:77111163	AATGCTTTAATAATA[-/T]TTTTTAATAAAATGT	23077
rs529000668	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77285940	GGAGCTATTAGAGTA[C/G]GTACAGTTAGGACAT	23077
rs529016260	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77234167	AAATAAATTTTAGTT[A/C]CAACTTAAAATTTTA	23077
rs529032687	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77185643	ATTAAACTTTATTAG[A/G]TTATTTAACTTTGGC	23077
rs529050527	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77316372	TGCCCCCAAGAATGA[G/T]CCATCACCTAGGGCC	23077
rs529055552	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77267674	TCTATTCTCTTGATA[C/T]GTATTAACTTCACGT	23077
rs529058677	in-del	-/A	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77188811	TTATCTGTGGTCTAG[-/A]ATATAAATGTGAATA	23077
rs529069594	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77216906	CACAAGACATTGTCA[A/G]AGGATTTGAGAAAAA	23077
rs529076385	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77302614	CATAATTCACTGTCA[A/G]GAGACCAATATTACA	23077
rs529086384	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77158815	GTTCTCTTGGGTGGG[C/T]GGGCACCAAGGTCTT	23077
rs529088330	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77108815	TTTACACCATTCTCC[C/T]GCCTCAGCTTCCTGA	23077
rs529097023	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77271446	GTAGTATGCATTTGG[A/G]TGCCAAAACAAATCT	23077
rs529103668	snp	C/T	0.000382641	0.0138266	intron-variant	MYCBP2	GRCh38.p7	13:77068558	AGGCTGTAGTGTGAT[C/T]AGTCACCTGTCTCTG	23077
rs529137045	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77100316	ACAGTAGTGCTGGAG[A/T]ATCTGCCCCAGTCTT	23077
rs529143476	snp	C/T	0.0142736	0.0832652	intron-variant	MYCBP2	GRCh38.p7	13:77242270	AGGCGCACACCACCA[C/T]GCCCAGCTAATTTTT	23077
rs529166409	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77163356	ACCAATATTAAGTGG[A/G]AGAAAAGGGATGGAG	23077
rs529179098	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77155318	AAATTAGCTACCCAA[A/T]GAGCAAAAAGGATTT	23077
rs529191520	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77170640	GGAGTGCAGTGGTGC[A/G]ATCTCGGCTCACTGC	23077
rs529199117	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77108841	CCTGAGTAGCTGGGA[A/C]TACAGGTGCCTGCCA	23077
rs529207784	snp	A/C/G	0.000280174	0.0118328	synonymous-codon	MYCBP2	GRCh38.p7	13:77217906	ATGGTTGCTGCCTGC[A/C/G]GTGACTTGTGTGCTA	23077
rs529212987	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77162787	CCAGCCTCCCGAGTA[C/G]CTGGGACTACAGGCA	23077
rs529235630	snp	A/G	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77264116	ATAAGGATAAACTCA[A/G]AAGGAGACTGTGCTT	23077
rs529242435	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77249687	GACATGGGCCACTAC[A/G]CCCAGCTAACACTGA	23077
rs529248081	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77201880	ACCAGAATCTCTGGG[A/T]CACATTCAAAGCAGT	23077
rs529260600	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77149846	GACAACTCACTAGTC[C/T]AACTGATCAGCATAT	23077
rs529275301	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77258098	CTCCTGAATGCTTCC[C/T]CCAAATGGTAATACC	23077
rs529276100	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77053050	GGCTGAGGTGGGAGG[C/T]TTGTTTGAGCCCAGG	23077
rs529286809	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77309896	AGGCGGGCAAATCAC[A/G]AGGTCAAGAGATGAA	23077
rs529300737	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77281328	TCAAATATTACTTCC[A/G]ATTTTTAATACCTCT	23077
rs529305914	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77156352	AGTGATAATCATGAG[C/T]GTCTCCCTCAGAAAC	23077
rs529312464	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77257447	GGAGACCCCATTTAC[A/C]CTGTGATTATTATTA	23077
rs529313617	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77085912	TTATGCAGGAACAGA[G/T]AGCTGTTACAGGTAT	23077
rs529316434	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77310814	CACACCATATTTAGG[C/T]ACAATACAGTCAAGC	23077
rs529337903	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77256481	TTATCAGTAAATATT[A/G]TCAAATAAATAAGAA	23077
rs529342948	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77187062	CAATCCTCCTGCCTC[A/G]GCCTCCAAAAGTGCT	23077
rs529355519	snp	C/T	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77202329	GACACATACACTCTC[C/T]CAAGACTAAACCAGG	23077
rs529370447	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77250371	GCAACTATTACAGAG[C/T]TGACAAAGAGGAAGG	23077
rs529382496	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77328530	TAGGTATCCAGTAAG[C/T]ATTTATTAGACTAAA	23077
rs529387170	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77295346	ACCATGTTGGCCAGG[A/T]TGGTCTCGACCTCTT	23077
rs529397829	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77311447	GACGATGCACATGTT[C/G]TAATTATCCAACAAT	23077
rs529399357	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77150623	CAAATTTAATATCCA[C/T]CAAATGCTCTTTGGA	23077
rs529404706	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77235881	AAAGGAGGTAACAAG[C/T]AGCATAAAGGTTCAG	23077
rs529432733	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77302956	AATACAAATCCACAA[C/T]TGAAAGAGTAAGTTC	23077
rs529444870	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77049291	CAAAGCCTGCTACTT[A/C]TATTAAAAAAAAACA	23077
rs529447939	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77086476	CTTCTTGACTCAATG[G/T]GTTGTTATCTGTAAT	23077
rs529468371	snp	G/T	1.65397e-05	0.00287569	intron-variant, nc-transcript-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076862	TACCTGATGAAGATA[G/T]GCATGTGAGAAGGAA	23077
rs529474856	snp	C/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77159579	CCTGGCGGGAGGTGA[C/T]TGAATCATGGGGGCA	23077
rs529490395	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77134585	CAACAAAAATAACAA[A/C]AAAAAAAAGGAAAAG	23077
rs529493384	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77287449	CTTGGCCTCCCAAAG[C/T]GCTGGGATTACAGGT	23077
rs529500044	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77190918	TATACTGTTATATAA[C/G]TTCAACTGATTTCAA	23077
rs529520281	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77273309	TCAGAGTTAAACATA[A/C]ATATCACTTAATTGA	23077
rs529534139	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326369	GAAAGCTCAATAAAT[A/G]CGCAGGTACACACAC	23077
rs529537537	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77143011	ACCCCTTTCCTTGAG[A/G]AGCATCAGGAAAAAT	23077
rs529538371	snp	A/G	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77242770	CCATTTCTAATAGTT[A/G]TTGATAGTAGGCAGA	23077
rs529572917	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77171325	AATAATTCTGCATTA[C/T]AGTATGGAGAGTGTG	23077
rs529591918	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77220686	GTTGTAGTTAATACA[C/T]ATGCTATAGAAGCTT	23077
rs529594572	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77126740	GCTATTTAAAATAAA[A/G]TTGAAGGCAAGAAAA	23077
rs529608183	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77094882	CACTAACATGTCTGA[C/G]TTGACATCCGAGTAT	23077
rs529608572	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77187817	TTTGGGAGGCCGAGG[C/T]GGGTGGGTCATGAGG	23077
rs529614103	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77116053	CTCTACCATTTTACT[A/G]TGTATGTTTCTGGGG	23077
rs529634982	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77077483	CAAGCTCAAATAACA[A/G]AGAATTGCACAGAGT	23077
rs529647128	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77305881	CAGGAACAGATTTTA[C/T]TTAATCTAATACAGA	23077
rs529647559	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77080857	TGAAGCAGGAGAATC[A/G]TTTGAACCTGGAGGC	23077
rs529660136	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77288089	AAGTATTTTAGCAAT[C/G]CGTATATATGCATTA	23077
rs529668387	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77152668	GCACCACTTAGGAGA[A/G]GAGCATGGCTGGAGA	23077
rs529673450	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77205922	CTTAAAGTGCTATTT[A/G]AGGAAGACACATTAG	23077
rs529673575	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77213609	ATTCCCTTACTACCA[A/T]CTAATATGAAGAAAA	23077
rs529704291	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77089241	CTATTAAGTTGTAGA[C/G]GTGGGTTTTGAATCA	23077
rs529708204	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77097206	AATATTAGAATTTAT[C/G]TGTTTTTCACAAAAC	23077
rs529710568	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77313411	ATTAAGAAAGCCAAA[A/T]GTTGGTTCTTTGGAT	23077
rs529720870	in-del	-/ACA			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77292482	ATGAACTATTGATAT[-/ACA]ACAACATTAACACAA	23077
rs529722076	in-del	-/AC	0.0256215	0.110247	intron-variant	MYCBP2	GRCh38.p7	13:77205027	ACATTGTGCACATGT[-/AC]CCTAAAACTTAAAGT	23077
rs529730109	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77152138	CAACGCGATTCTATG[A/G]AATCAGTAGTTTGAG	23077
rs529751646	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77207466	AAGTGAGGGATGCAA[A/G]CTATTGTTTAATAAC	23077
rs529769874	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77190118	TGTTAAATATATTTA[C/T]AGTTCTACCAGCATA	23077
rs529769977	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77048931	ACATAGAGGAAACTT[G/T]AAGTAAAATCTAGAT	23077
rs529778410	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77245162	ACTGTTGGTGGGAGT[A/G]TAAATTAGTTCAACC	23077
rs529786712	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77289976	GCAAACCACATATCC[A/C]ACAAAGGATGAGTAT	23077
rs529787597	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77049759	TCTGGCCTCAGCCTC[A/G]TGAGTAGCTCGGATT	23077
rs529792813	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77298702	ACTAAGGAGTTATCC[C/T]TGGGATTATTTTGCA	23077
rs529803191	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77149748	TCAATATGTGAATTT[A/C]ATCTTTTATTTCCTA	23077
rs529808832	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77198431	AAGAGTGTTAACATA[A/T]TGATATCATTTTTAG	23077
rs529809465	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77153043	GTACTCCAGCCTGGG[C/T]GACAGAGCGAGACTC	23077
rs529843185	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77261492	AAATTCACATAAAAA[A/C]AAACTCTTTTTTACA	23077
rs529854166	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77245833	AAAATAATACATATA[C/T]ATGTATATATATATG	23077
rs529880108	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77174564	AACTCTAGCAGTAAA[A/C]TAGGCAAATATACTG	23077
rs529955710	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77130441	TACATATATATGTAC[A/G]GATGAATGTGGGTAC	23077
rs529961738	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77276566	AGGATGGAAGACAGA[C/T]GAAAGGCAGTACAGC	23077
rs529975804	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77183853	GTGCCCGGTGAACCC[C/T]TATTTCACTTTTGAT	23077
rs529975957	snp	C/G/T	1.64746e-05	0.00287002	synonymous-codon	MYCBP2	GRCh38.p7	13:77174385	GCTGCACGTGCTGAA[C/G/T]GTGAATGTCACACCA	23077
rs529987146	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081251	TGGAATTCCACAGTG[C/T]TCCCAATCATATTAA	23077
rs530008341	snp	C/G/T			intron-variant	MYCBP2	GRCh38.p7	13:77153508	CATACTATTTCAATT[C/G/T]AACCTTTCTGTAAGC	23077
rs530024472	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77122858	TGATTTAAAAAACCA[A/G]TCTTAGCACTTCCCT	23077
rs530033161	snp	A/G	0.0174175	0.0916809	intron-variant	MYCBP2	GRCh38.p7	13:77058974	TGGGCGACACAGCCA[A/G]ACTCCGTCTCAAAAA	23077
rs530041216	in-del	-/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77282916	TTAACATTTCCTATA[-/T]TCAAAACACTGTCAC	23077
rs530061316	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77269321	ATTTGGCCTCAGGAC[A/G]TGTATACATTTCCAA	23077
rs530065655	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77277247	AAAACCGAGCAAAAT[A/G]TTGTTAAATAAAATA	23077
rs530066499	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77066603	ACATCCTTGCATATA[C/T]ACCTTGGTGCAAATG	23077
rs530069916	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77183318	TTGACATTATTTCTT[C/T]CTTAAATGTTTAACA	23077
rs530081045	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77231946	TTCCTTAAATATTTA[C/T]GGCATTGTTAGAGCA	23077
rs530090093	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77107266	TATTTGAGAAATTAA[C/T]TTTTAAATTATTTAT	23077
rs530092498	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77113530	AAGATGGTAATGAAG[A/G]GTGAAATAAACACAG	23077
rs530108504	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77321825	AGTCTAGAATTTGTG[C/T]CTTATAAATTTTTAT	23077
rs530115499	snp	A/C	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77161298	GACGTAACAGATCCA[A/C]AGGGGGTATTGCACT	23077
rs530120200	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77074201	CCAGAAACAGACCTA[C/T]CATTTATGGTAAATT	23077
rs530129239	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77262289	AAATATTAACCATAG[A/G]TATAGTACTCCAAGG	23077
rs530130818	snp	A/G	1.65351e-05	0.00287528	intron-variant	MYCBP2	GRCh38.p7	13:77066094	TCGGAGATAACTACA[A/G]GAAAAATTAGCACTT	23077
rs530187065	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77146878	CATGCCCTACAACTT[A/C]ACAATTCCACTTCTA	23077
rs530188454	snp	A/G	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77132248	TATTAACAAAATCAG[A/G]AAATCTGGGGTATGT	23077
rs530239621	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77263321	TTTTTAAATAGTTGA[A/C]AAATGATGCAGCATA	23077
rs530245937	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77314621	GGCAGAGAAACAGGA[A/C]TAGGTGGAGCACAGA	23077
rs530258500	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77050899	TTAGGCTAGTTTGAA[C/T]TGAGTTTCTGTCACT	23077
rs530269669	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77299584	TAGTAATATAACACA[C/T]CATTATATCTCTATA	23077
rs530277977	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77051526	TCACTGAAGAGGGGA[A/G]AACCTAAAAGTTTCA	23077
rs530302330	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77207980	CGCCCCAGCCCCAGA[C/T]GAATGAGTATTTGAC	23077
rs530303175	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77193788	ACATGACCACTTGAC[A/G]CTAATTATTTATTAC	23077
rs530305036	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77108068	CTAAAAGAATCATGC[C/T]AATAGAATGAAAGAA	23077
rs530310556	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77247820	CAATAGAGAAAGGAT[A/C]ATCATTTCAATAAAC	23077
rs530334406	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77307433	AAAAATGGTCCTGGC[C/G]TGGGCAACATAGCAA	23077
rs530349468	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77215546	ACAGGTAAGAAAGAA[C/T]CTTGTGGGAATGGAT	23077
rs530367066	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77300373	ACGAAAGCAGCCATC[A/G]GCAGCACATAAAGAG	23077
rs530368486	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77266759	ATGAAAAAAAAAAAA[A/C]AAAAAAAAACCCTGT	23077
rs530381890	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77307150	TATGTCCCTGAGACC[A/T]TTTCAAATCTGAAAC	23077
rs530400359	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77301186	TTGGGAAGCTGAGGC[A/G]GGCAGATTACTTGAG	23077
rs530413500	snp	A/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77105742	AATTTTGATTCTTTT[A/T]TGGGTATCACTAAGT	23077
rs530439016	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77153130	TTTCAAACCATTCAT[A/G]TGACCTGATTCTTCC	23077
rs530451820	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77099239	TTTCATGGACGCAAA[A/C]CAACAGGTTGAACAA	23077
rs530468990	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77279459	GTTACTAAAGATTGA[A/G]AGAGCAAATTGCAAT	23077
rs530475865	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77192545	TGAAAGAAGAATAAA[A/G]GGCATTTAAAGAAGC	23077
rs530484741	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77298814	GAAAGAGAAAGATTA[A/G]CAGTGCCAAATGCTA	23077
rs530493860	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77254866	TGTCTCTGTCCCTGG[C/T]TTATTTTATTGCAGT	23077
rs530495313	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081399	CTGAAAAGAGCTAAA[C/G]AGCCGTAAATCACGT	23077
rs530527774	snp	G/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77194922	AAAAAGAGGGGAAGA[G/T]CCTCTGGGTAAGAAA	23077
rs530530755	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77254244	AAAATATAAAAGAAC[A/G]TGTAAAAATATATAA	23077
rs530555947	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77090369	ATTTCATGTGGAGAA[A/G]CAAAATCAAAGCCAA	23077
rs530557828	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77191513	CTCCTTGTTCTGTCT[A/G]GACCTCAATTTGGCA	23077
rs530565505	snp	C/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77299380	CCCATCAATTCTTAA[C/G]TACAGGCCATCCAAG	23077
rs530581248	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77183169	TTTTAAGAGCATCTA[C/T]GTTTCTGAGTGATAT	23077
rs530588052	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77131262	TAGTGCATGCCTATA[C/G]TCGTAGCTATTCAGA	23077
rs530593867	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77221309	TATCTCTTCAGACTT[A/G]GGAATCGAAGAATGG	23077
rs530595179	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77321853	TATAGGGCCAATGGT[C/T]AGTGCCAAGTAATAA	23077
rs530600398	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77091189	CTCACCACTTCTCTA[A/T]GCTTATGTACATTCT	23077
rs530614136	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77138890	GCTGTATAAATAAGA[A/T]AGAAAAAAATGTAAC	23077
rs530631478	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77183919	CCCAGTCAGGTTTGC[C/T]AGGAGTTTACCAACT	23077
rs530656378	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77069811	AGGCGGAGCTTGCAG[C/T]GGGCCGAGATCGCAC	23077
rs530665337	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77239087	ATCGCACCACTGCAC[C/T]CCAGCCTGGGTAACA	23077
rs530729135	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77233002	CAGTCACTGACAAAC[A/G]GTATCACTTTCAGAA	23077
rs530729141	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77222903	ATGTAAAGGAGAAAC[C/T]ATAGAAGTCCCCTTG	23077
rs530738384	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77249548	TCAGAGAGTGGGGAT[A/G]TTAAATTTTATTTTT	23077
rs530739936	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77073646	AAGAAAACCCCAAAG[A/G]GTCTATAAAAAGTTT	23077
rs530740866	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77175497	ACAATAAAAGCTTTT[C/T]GGTTTTTCAGTATCT	23077
rs530749320	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77283989	AGTGACAGTTTGAGC[C/T]GGTTAAAAAACTTAA	23077
rs530755372	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77139604	CTTTAAGATACATAA[A/T]CAGTAAAATCAGATG	23077
rs530779864	snp	A/C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77278023	TGAAAGGCAAGAATC[A/C/G]GAACATACTTTAAGA	23077
rs530792903	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77115165	TACAGTCAATAAACA[C/T]TCCTTGAATGCCTGT	23077
rs530798964	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77107342	TATAAATTATGCCTT[C/T]AACTTGGCCAAAAGA	23077
rs530800702	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77215681	AGCCTCGACCTCCAG[A/G]GCTCAAGTGATCCTC	23077
rs530803594	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77322063	TACTGGAGGAGACTG[A/G]GGCAGGAAGATCACT	23077
rs530812803	snp	A/G	5.01895e-05	0.00500921	intron-variant	MYCBP2	GRCh38.p7	13:77168687	AAATGAGATACACGT[A/G]AAAGTGGTTCTAAAA	23077
rs530822486	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77176286	CAAAACTTCCTACTA[C/T]TCCTGACTTTAAGAA	23077
rs530826834	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77117940	ACAATTTGAGAAAAC[C/T]GGGAAAACTAAATTG	23077
rs530831941	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77122002	TTAACTTTTAACTTA[A/T]TTTATCACATAAAGA	23077
rs530844904	in-del	-/T	0.225597	0.248806	intron-variant	MYCBP2	GRCh38.p7	13:77059060	TCACCAAAATGCAGA[-/T]TTTTTTTTTTTTTTA	23077
rs530847480	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77101003	CAGCATATGGCAAAT[C/T]TGGTAAACAAATTAT	23077
rs530853647	snp	A/G	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77066879	CTACTGGCATTTATA[A/G]GTTTTTTTCTGTGAA	23077
rs530867360	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77277364	CACGGTGCTTGCCTG[A/C]CAACATGACAGCTTC	23077
rs530867991	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77099432	AATTTCCAGCAGAGT[C/G]ATACCTCGCATCCTT	23077
rs530875253	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77288594	AACCAATCTGACAAG[C/G]GCTGGAAAAGGATGG	23077
rs530886393	snp	G/T			synonymous-codon, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076790	AGGTGATGACAATAG[G/T]GCTTTTTCCTCTTGT	23077
rs530888205	snp	A/G	1.65562e-05	0.00287712	intron-variant	MYCBP2	GRCh38.p7	13:77161874	TTTAAATTAATGTAC[A/G]AAGTTTATCCTTAAA	23077
rs530891777	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77058854	ACCAGGCATGGTGGC[A/G]CGCGCCTGTAATCCC	23077
rs530901550	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77255894	TTCAACGCTTAGTTC[C/T]AATAATATATATGTA	23077
rs530907071	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77154764	GTGATCAAAAATCTG[C/T]CCTTGAGTAGTAATT	23077
rs530910137	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77231992	AATCACAAATTTTAC[C/T]GTGGTTAATTGCATT	23077
rs530933508	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77108260	GAAAACATACTCATA[A/G]CATATTATTGAATAT	23077
rs530943928	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77101670	TAGGCATACAAATAA[C/T]GGCAGAAATATTTCT	23077
rs530955944	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77067446	TATACATGACCTTTT[C/T]AGATATTAGCCAGTT	23077
rs530965396	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77301249	GTGAAACCCCGTCTC[C/T]ACTAAAAATGCAAAA	23077
rs530978498	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77069819	CTTGCAGTGGGCCGA[A/G]ATCGCACCACTGCAC	23077
rs530995347	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77200038	CGGAACAAAGCTGGA[A/T]GGAGAATGACTTTGA	23077
rs530996552	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77286680	AGAATGGCCTGAACC[C/T]GGGAGGCGGAGCTTG	23077
rs531003107	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77210293	CGCCTCCCAGGTTCA[C/T]GCCATTCTCCTGCCT	23077
rs531018995	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77256606	AAGTAGACATATGAA[C/T]AGCAAACAGGTATAT	23077
rs531020119	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77051597	CATTGTTTAACTATG[A/G]TGATCATTTCATGGA	23077
rs531020908	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77247979	AGGAACATCACACAC[C/T]GGGGCCTGTTGTGGG	23077
rs531046951	snp	A/C	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77147590	TTTGTTTTCATAAAA[A/C]TGAATTAGAAATGAT	23077
rs531050305	snp	C/T	0.0162398	0.0886349	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77074019	CCCCCCCCCTTTTTT[C/T]TTTAAAGAAACGGTC	23077
rs531058641	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77316147	CAGAAAGAAAGACAA[C/T]ATGATTATTTACACA	23077
rs531062843	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77308319	ACTCTATTAATTATT[C/T]CCATTCTCTCTCTCT	23077
rs531063514	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77185759	TCTCCCCTCATTTTA[A/G]AAGCAGCTTAAATGC	23077
rs531086884	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77148688	CTGTTATTCACAAAT[A/G]ATCTTCAATTTCAAC	23077
rs531103486	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77193895	GAAAGTAAAGGTGTA[C/T]AAAATATATGCATAT	23077
rs531133956	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77166771	TTTCATAAATTTGAC[C/T]TCAAAGTATGTAATT	23077
rs531181313	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77263539	TAATAGTAACAGACA[C/T]AAAATAGCTGCTACA	23077
rs531186372	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77244413	CATGTAATATGTCTC[C/T]TTCCCATTCCCTATT	23077
rs531193655	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77110183	CAGATGTGCAAGTAG[A/G]AGAGATATCACTAAA	23077
rs531219124	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77294517	ACAAAGCTAGTTGGA[A/G]GCCGAATTGAAGGGG	23077
rs531237388	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77227716	TAAATGTATTGATGC[C/T]TAGTTATAAGGTTTT	23077
rs531246597	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77127801	GATTCAAGAATTCTG[A/T]ATACCTGCTACTTTG	23077
rs531263957	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	MYCBP2	GRCh38.p7	13:77045319	GAGTTTAAACTTCAC[C/T]GCATCCTCTTGGGGG	23077
rs531268469	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77083488	TATGCATGTGTATGT[A/G]TAGTGTGTGTGCATA	23077
rs531272780	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77092916	ACTCTGATTTACTAC[A/G]GCATTAAGTAATGTC	23077
rs531275516	snp	A/G	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77212908	TTCCACCCCTGGCTC[A/G]GGACCTCTCTCCCCT	23077
rs531302442	snp	C/T	0.00250178	0.0352793	intron-variant	MYCBP2	GRCh38.p7	13:77165429	GTTCAAACTCTAAAA[C/T]AATTTTATAAAAATT	23077
rs531329091	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77318670	GAGGCAGAAGAATCA[C/G]TTGAACCTGGCAGGC	23077
rs531347180	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77327008	CCCCGCCACCCCGGG[A/G]ATGTGAGGAGGAGGC	23077
rs531354836	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77143905	TAGAAAAGGTACAGG[A/C]AAATCTTATAGGACC	23077
rs531356167	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77172040	CAAATAGCTGGGATT[A/G]TAGGCATGCACCACC	23077
rs531356411	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77152004	TGGTTGGCAAGAACA[C/G]GTAATTCAACAGAAT	23077
rs531357415	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77120991	GAAGTAATAGTTTGA[C/T]TTTAAATGGATCATT	23077
rs531389947	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77289247	CATCAAAAAGTTAAA[C/T]TGGCATGGCATATAA	23077
rs531399009	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77103404	AAGCATTTCAAATGG[C/T]ATGCAAGTATAAACT	23077
rs531413431	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77092875	AATGCCACTGCTCCC[A/G]TGAAAACTCAAAGTA	23077
rs531414609	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77259526	TTATTTTTAAACTGT[A/G]CAAGAACCCACTCCC	23077
rs531416218	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77151340	TCTCAGCACATTTTA[A/C]AGCACTAATGTCAGT	23077
rs531418036	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77251374	TTTGACAGATCAATT[C/T]GTAATTTTTATACAG	23077
rs531427000	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77054843	AGAGCTCAAGAAATC[C/T]GCCCACCTTGGCCTC	23077
rs531439070	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77212341	TATTTATAAAGTAAT[A/G]AAATAATTTCTATTA	23077
rs531450883	snp	A/G			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77293665	TACAAGTGAAAGAGG[A/G]AGGCTGGACAGTAAG	23077
rs531463044	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77165408	TAATAAAAATGCCAG[A/C]ATTGAGTTCAAACTC	23077
rs531468024	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77319278	TCTGCAAGCAACCCC[C/T]CTAGCTAGTAGAAGA	23077
rs531471082	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77288910	AGATGCTTCCCTAAG[C/T]TCTCTCTCACCTATC	23077
rs531489627	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77144295	TGCACTAATTAAATA[C/T]TCATTATGAAAGAGA	23077
rs531492043	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77304315	AAAAGAGTAAAATTC[C/T]GTCATTTGCAGCACC	23077
rs531510937	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77197293	CTAGGTGGCTAGTCC[A/T]AGACAAATACCTTTG	23077
rs531531323	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77095192	TACCTATTACCATAA[A/C]GTCATTATGTCAGTC	23077
rs531543987	snp	C/T	1.69255e-05	0.00290903	intron-variant	MYCBP2	GRCh38.p7	13:77095644	CTTTTCTGACTTACA[C/T]TAAAATCCTTAGTTT	23077
rs531552818	in-del	-/A	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77207629	CAATTAAAAAATTTT[-/A]AATTATTTTTAAAAA	23077
rs531567012	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77237965	GTAATAGCAACATGC[C/T]GGACGCGGTGGCTCA	23077
rs531586439	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77189251	TTCCTTTAAATCCTA[C/G]CTTCGCAAGACCGAG	23077
rs531609406	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77088121	TCACTGAAAGCACAC[A/G]GAACTTGAAACAGTT	23077
rs531620243	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77244352	AGCAGATAAGTGAAG[A/G]CAGGTGTTGGTAGCC	23077
rs531654076	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77245081	CGCCAGTTACAATGG[C/T]GATCATTAAAAAGTC	23077
rs531673237	snp	A/C/G	0.000270741	0.0116317	intron-variant, nc-transcript-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087640	GTTGAAAGCCTGAAG[A/C/G]AATGACGGTTAAATG	23077
rs531683145	in-del	-/CAA			intron-variant	MYCBP2	GRCh38.p7	13:77130967	AAGTGCTTTCTCAGT[-/CAA]CAACATGTACAATGA	23077
rs531690335	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228999	CATTAAAACAAATCA[C/G]CAAGGACAAAAGTAG	23077
rs531731175	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77306553	AAAAAGAAAAGAGGG[G/T]AGGGGAATATGGAAG	23077
rs531746298	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77079439	TACATGTTCAAACTA[C/G]TGTCAAATATCTTAA	23077
rs531760057	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77182207	ATCCTCACAATCACA[A/G]TACTCTCTAGCACTG	23077
rs531784253	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77313685	AAGACAAGGCACAGA[C/T]TGAAAGAAAATATTT	23077
rs531789896	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77275667	GTCCCTAAAGATAAA[C/T]AAATAAAAAATTTTT	23077
rs531794839	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77049778	GTAGCTCGGATTACA[C/G]GTACCCGCCACCATG	23077
rs531828422	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77269630	GATTCTGTCTCAATT[-/A]AAAAAAAAAATGTGC	23077
rs531835088	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77160681	GAAACCTATGAAGTG[C/T]TCTACAGATATTATT	23077
rs531869311	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77230067	TTACTGTATTTTATA[G/T]GGAATTTTACTTATT	23077
rs531874074	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77158800	GAGTAAGGTGTGTCT[C/G]TTCTCTTGGGTGGGT	23077
rs531879394	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77207619	TTTTTTACCACAATT[A/T]AAAAATTTTAAATTA	23077
rs531881949	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77080168	GAGGAAATAGCTCAT[A/G]TTATATTAGCTAAGC	23077
rs531886898	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77160248	ATGAGACGGGGTTTC[C/T]TTTGTCACCAAACTG	23077
rs531889500	in-del	-/G			intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77074010	CCCACCGCCCCCCCC[-/G]CCTTTTTTTTTTAAA	23077
rs531901104	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77175946	TGGGCGACAGAGTGA[A/G]ACTCCATCTAAAAAA	23077
rs531909060	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77187202	ACTTAAACATAAATA[A/C]AAAGGGGTTACCAAG	23077
rs531917853	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77214212	TGTGGAAACAGGCAA[A/T]CTCATACACCGTTAG	23077
rs531919228	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77112598	GCCCAGCTGATCTTT[A/G]AAAAAATTTTTCTTA	23077
rs531920420	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77167407	GTCTGAAAGAACCAG[C/T]AGGTAAGCTGAAGAG	23077
rs531931692	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77221915	ACATAAACTACACAT[C/T]CTCCTGTATACTTTA	23077
rs531934108	in-del	-/TTATAGCAGC	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77048378	GTTTACAGTATTTTG[-/TTATAGCAGC]TTGAATGGATGAAGA	23077
rs531939889	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77320319	AGCCTAACCACAGCA[A/C]CTGCCACACCACCAC	23077
rs531945292	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77269198	TCTCTCTTGTGATTC[C/T]TTGCATATTCTTCAT	23077
rs531951503	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77213553	TTTTGGAGGAAAAAT[A/G]AATTAGTTATCTTTT	23077
rs531961369	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77111454	TTTTTTTTTTTTTTT[A/G]AGAGGCAGGGTCTTG	23077
rs531963296	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77103536	TTAAGGTCCAAATTT[C/G]TTAACTTAAAACTTA	23077
rs531971022	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77221400	AGCTGACATGAACAC[C/T]TTCCCTCTCAGCGGC	23077
rs531981262	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77120907	TTAACTAAGATTACT[A/G]GGTTAGAAATTCAAA	23077
rs531993209	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77096996	AAGCCTATAGAAATC[A/T]ATCTAATCTAATTTA	23077
rs532002763	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77106554	AAAAATTTTTTTCAA[A/G]GACATTCCACTGGGA	23077
rs532005361	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77220542	ACCACAATATTGATC[C/T]TAAACAACACATTAT	23077
rs532038321	snp	A/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77212400	TTTTTTAAAAAAAAG[A/T]TTGAAATATTTTCCA	23077
rs532041820	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77261551	AATACACATATTTTG[C/T]CAAGAAGACACAGTT	23077
rs532052373	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77119568	CTTACAAAAAACAGC[C/T]CTTCGATCTTGGACA	23077
rs532059085	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77113294	AAGCTTTCCTATGTT[G/T]CCATTGCATCCTGTG	23077
rs532066715	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77252086	CACTACCTCCTCAGT[A/G]CCTGTTTATACCTCA	23077
rs532070439	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77159721	CCTTCTGCCATGATT[C/G]TAAGTTTCCTGAGGC	23077
rs532078168	snp	A/G	0.00597247	0.0543191	intron-variant	MYCBP2	GRCh38.p7	13:77194099	ATTCATTTATAATAA[A/G]TTTTTAATATTAAGT	23077
rs532089555	in-del	-/CTC	0.00478085	0.0486577	cds-indel, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326927	GACAGCGACCTCCTT[-/CTC]CTCCTCCTTCTTCTC	23077
rs532106180	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77158646	AGAGATGGGGTCTTG[C/G]TATGTTGCCCAGGCT	23077
rs532130465	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77312384	TCGACAACAAAAACT[A/G]TAACATTGTTTGGTG	23077
rs532143291	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77320730	ACCTCACAACCTCTG[A/G]ATGGGATGCAACATG	23077
rs532143419	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77313234	AGATAAAAATTCATA[C/G]CTTTAAATACTTATA	23077
rs532146069	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77137163	CTTCTTTCCCTGACC[C/T]TAAGGAGACTGTCTA	23077
rs532149170	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77048727	GAAAATGCCCAGGAC[C/T]GAGGTCATTCCTTCC	23077
rs532154853	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77054897	TGAGCCACTGTGCCC[A/G]GCCAAGATTGATGAA	23077
rs532167459	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77165650	ACTCCCCTGCTTAAT[A/G]AAGTACTTCAGTTAC	23077
rs532178774	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77244441	ATTTAATAAATGGTG[C/T]TGGGAAAACTGGCTA	23077
rs532181812	in-del	-/GC			intron-variant	MYCBP2	GRCh38.p7	13:77319019	TTTGTGACAGATATT[-/GC]GCTGTGTTTCCTTTA	23077
rs532182264	snp	A/C	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77144996	CATGCATCATCAATT[A/C]CTCTCAATTTAGTGA	23077
rs532183680	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77288586	CAATAACCAACCAAT[C/T]TGACAAGGGCTGGAA	23077
rs532189688	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77095843	TTAACACCTAACTAG[A/T]TAAATCTAAATGTAA	23077
rs532213359	snp	G/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77197793	AGAGGTGAAGGGAAG[G/T]AAAAAAAAAGACTGA	23077
rs532213916	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77230899	TGTTGGTGCTCAAAA[A/G]GTTTCAGATCTTGGA	23077
rs532233683	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77152104	AACTACAGACTGTCT[C/T]TATGTTTATTGTTCT	23077
rs532240552	snp	C/T			missense	MYCBP2	GRCh38.p7	13:77188998	AAATGTGTACAGGTT[C/T]ACTGGTTTGCTGTTT	23077
rs532271410	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291000	AAACAAAAAAGTGTT[G/T]CTGAGTGAAATTTAA	23077
rs532275373	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77170792	ATGTTGCTCAGGCTC[A/G]TCTCAAACTCCTGAC	23077
rs532282236	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77138115	ATTTTACTTATAGAT[A/G]TATCATTGTTCAACT	23077
rs532325320	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77189263	CTACCTTCGCAAGAC[C/T]GAGTAGTAGAGGCTT	23077
rs532331069	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77088174	AAAAAAACAGGAAAA[A/G]TAATTTATAAGATAC	23077
rs532338594	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77089145	TTTTTGAACATGACA[C/T]AAATCATAACAATTT	23077
rs532346438	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77259276	TCTCAAAAAAAAAAA[A/G]TGTTGGTGCTAGGAT	23077
rs532347472	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77275709	GGAATCTTGGCCAGG[C/T]GCAGTGGCTCATGCC	23077
rs532350849	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77196905	ACTATGAGGAAGAGA[A/G]TACTTTTAAAAGATG	23077
rs532364439	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77230794	GGGCTGAGAGGATTG[C/T]TTTCACTTTAGGACA	23077
rs532372004	snp	C/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77305667	GTATGTGTATTACCC[C/G]TTTTATTTTTAAAAA	23077
rs532375086	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77207568	ACCACTGACTGCAGA[C/T]TTTCAAAATGATTAA	23077
rs532380273	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77283668	TTGGAAGGCTGAGGC[A/G]GTCAGACTGCTTGAG	23077
rs532412300	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77237981	GGACGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC	23077
rs532438101	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77289868	ATTACTATATAAAAA[G/T]GAGTAGTATATCCAC	23077
rs532440772	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77238595	AGTTATCACAAACCA[C/T]TGAACTAAAATCTAT	23077
rs532457086	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77113448	GCTCATCACCATAAC[C/T]TAGCACAGAGTAGAT	23077
rs532484377	snp	A/C	0.00478085	0.0486577	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77079573	CAAATGCTGTGTACA[A/C]GGCTCTGTGGTAGGC	23077
rs532484737	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77167521	ACTTATAGATTTAAA[A/G]GGACTTAAGATTAAA	23077
rs532486925	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77065934	TTCAGCAGAGTAAGC[C/T]GTTTTGTGTCAGCTT	23077
rs532507985	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77276339	TAACACGAAAACAAC[C/T]GAATGGGAAAAAAAG	23077
rs532511554	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77221546	ACTTCCCTTTCCACT[C/G]TGGCAAGACCATGAA	23077
rs532518436	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77121950	AATTTTCATTTGTTA[A/C]CTGTTCTAAGTTATG	23077
rs532531219	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77045678	CACTATAAAAAATTC[A/G]ACACAGATATGTACA	23077
rs532550261	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77314547	GTATGATTTCAACTA[C/T]AGCACATTCTGGAAA	23077
rs532554159	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77328620	CCCTGGAGTGAGAAC[C/T]AAGACAATGGTGTAG	23077
rs532619521	snp	A/C/T	9.98493e-05	0.0070651	synonymous-codon, missense	MYCBP2	GRCh38.p7	13:77057022	AAATCCAAATGTTAT[A/C/T]CTTGGGCCAAGCCAT	23077
rs532623987	snp	C/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77056401	AGGGAGAGCTTAATA[C/G]AACAAAAAGGGGCGA	23077
rs532661284	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77199627	GCAGTAACCTCTGCA[A/G]ACTTAAATGTCCCTG	23077
rs532662222	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77154023	ATTGAAATATTAGCT[A/G]CAAATCAACTTTTAT	23077
rs532683266	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77255082	AGGCATCTCTCTGAC[A/G]TACAGATTTCCTTTC	23077
rs532688546	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77065256	ATTCAATGAACACCC[C/T]GAGAAAGTCTGTTTG	23077
rs532693378	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77162858	GACGGGGTTTCACTG[C/T]GTTAGCCAGGATGGT	23077
rs532696629	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77153411	GCCACACGACACCCA[C/T]GTCCCAAGTCCCACA	23077
rs532702346	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77307219	CTATCCAAGTATGCA[A/C]TTCCTCTCATACACC	23077
rs532703831	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77208673	TAAAAGGTGTCAGAT[G/T]ATATAAATCAAACTT	23077
rs532719250	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77235682	ACAAGATACAATCTC[C/T]GCTTCAAGAAGCTCA	23077
rs532725922	snp	A/G	5.10547e-05	0.0050522	intron-variant	MYCBP2	GRCh38.p7	13:77262139	CTGTACCTGAAATAC[A/G]AGACTAATAAATACT	23077
rs532732795	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77134318	GTGGATCACTTGAGG[C/T]CAGGAGTTCGAGAGC	23077
rs532732988	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77191346	TTTAATATCACATAT[C/T]TACTTCTTTTTTATG	23077
rs532746896	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77286839	TCCAGTCTTAAATAT[A/C]CCAATACTTAAACAG	23077
rs532755109	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77314033	GCTTTAATGCAAGAG[G/T]AACTCTCATTTATTG	23077
rs532758409	in-del	-/TGTTCATGGTTCATGT	0.00438332	0.0466095	intron-variant	MYCBP2	GRCh38.p7	13:77264295	ACATGCACCACGATG[-/TGTTCATGGTTCATGT]AACAAACTATAATGT	23077
rs532759203	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77261694	AACAGATATAATAAT[A/T]ATAAAGAAGTCTGAA	23077
rs532764230	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77262785	ATATGGTACATTTTA[C/T]GACTTTGTCCAGCTA	23077
rs532789371	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77214376	AAAGTATTGGAAACC[A/T]CGTAAATATATAAAC	23077
rs532805689	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77177633	AGTCTTTTTCAATTT[C/T]TTTAGTGTCATTCAT	23077
rs532807306	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77090599	ACAGTCAGATATAAT[C/T]GTAAGTGCACCAAAT	23077
rs532813056	snp	A/G	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291592	CCTCCACATGGAGAA[A/G]CCCCGTCTCTACTAA	23077
rs532835036	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77146155	ACTTTGAGAAAACGA[A/T]CCTTACCTCTTAGGA	23077
rs532837177	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77050856	AAAGTCATAAGCTTA[A/C]AAGGATCAAGGAATT	23077
rs532849337	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77199130	TTCCATCTGAGGTAC[C/T]GGGTTCATCTCACTA	23077
rs532858507	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77325270	CAATTGCCTAATAAA[C/T]TGCACATTCAATAAA	23077
rs532869940	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77059718	GCAAACTAGGTTTGT[A/G]TAAGTTGCTATCCTT	23077
rs532876613	snp	A/T	0.00597247	0.0543191	intron-variant	MYCBP2	GRCh38.p7	13:77135840	GTTTTTATCTTTTTT[A/T]TCTTTTTTTTTTTTG	23077
rs532890358	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77116159	CTGTATCAAAGTGCT[G/T]AAGTACAGTGTTTAC	23077
rs532897932	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77236316	TAGAAGCTACACTCA[C/T]GTGTAGACAATGGGT	23077
rs532902722	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77234730	AATATGAACAAAATG[C/T]CTTATTTTCTTAACA	23077
rs532904017	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77279533	AGACAAATTCCATTT[C/T]TCAGGCAATGTCAAC	23077
rs532905728	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77224758	ATACACACTTAAAAA[C/T]TCGTATAAATGCCAT	23077
rs532923528	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77099557	AAGAGTTGCTTAAGA[A/G]GCACTCTGTTTTATG	23077
rs532925251	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77164170	CTTTTGGTTTAATAC[A/T]ATATATTCAGTGCTT	23077
rs532933319	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77209650	ATGATCACAAAAGAC[C/G]ACTCACCCATAGTCT	23077
rs532962959	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77247339	AAAAGGAAATTACAG[A/G]AACAATTCCATAGCA	23077
rs532975646	snp	A/C	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77273082	AATCAAAAATATATC[A/C]GATTGATACCATATC	23077
rs532983468	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77163459	ATAACAGTGGGAAGA[A/G]TAATCTTCAATGAAG	23077
rs532993142	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77317117	AACATGCCCGGCTAA[C/T]TGTTTTGTATTTGTA	23077
rs532998904	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77264745	GATACCAGTATTACA[A/G]AAGGACCACAGGAAC	23077
rs533000556	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77277241	TCCAAGAAAACCGAG[C/T]AAAATATTGTTAAAT	23077
rs533028968	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77069404	GAGGCGGGCGGATCA[C/T]GAGATCAGGAGATCG	23077
rs533034491	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77093762	TGGTTCATGCTTATT[A/C]TTTCTTGCACAGACC	23077
rs533073215	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77225377	ATCAAATCTGAAGAA[A/G]TAAGTTACTGAGCAC	23077
rs533074639	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77150083	CTACCTTGATAATTC[C/G]GATTAACATTGCCTC	23077
rs533094295	in-del	-/AGG			intron-variant	MYCBP2	GRCh38.p7	13:77055180	AATGACTAGAAAGGA[-/AGG]AGGACAGAAAAAGAG	23077
rs533106098	snp	A/T	2.22254e-05	0.0033335	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076716	AAAAAAGAATAAAAA[A/T]GGGAAATAAATATCT	23077
rs533134922	snp	C/T	0.00438332	0.0466095	intron-variant	MYCBP2	GRCh38.p7	13:77295376	TGACCTCGTGATCTG[C/T]CAGCCTCGGCCTCCC	23077
rs533136090	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77196653	TTTTGGCCTGAGGAA[A/C]CAGAAGAATGAAGTT	23077
rs533138950	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77242877	AAATACCTAAACGTA[C/T]GTTATTAGAAGAAGC	23077
rs533149339	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77317805	AGCTGGGCGTGGTGA[A/T]GTGCACCTGTAGTCC	23077
rs533177763	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77303087	TGCCTGTAATCCCAG[A/C]ACTTTGGGAGGCCAA	23077
rs533181618	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77305831	AAGTATTTTTAAAAC[A/T]CAACAACCACTAGTG	23077
rs533195938	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77116880	TTTTTGTAAAGACTT[A/G]CAATGATTCTTTAGC	23077
rs533213504	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77314726	CCAAAAAATGTATAA[A/C]CCCAAGAGTGAACCC	23077
rs533218130	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77202434	AAGAGTCCAGGACCA[C/G]ATGGATTCACAGCCG	23077
rs533227444	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77077666	CAGGCCTGACTACGA[C/T]ATGGCTTCCGAGCAA	23077
rs533238678	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087353	ATTAATACTTTGCCC[A/G]TAGCACTAAAATATT	23077
rs533253547	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77258131	TCCACAGTACTTTCA[A/G]ACTTTTCTGGTCTAA	23077
rs533253897	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77157414	TTTTTTGTAGACACA[C/G]GATTTCACCATGTTG	23077
rs533256116	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77211162	TTATAAACTGAGATG[C/T]TTACCTCCAAATTAC	23077
rs533269790	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77287578	ATGCAGAAGTTCAGT[C/T]GGTTCATAGGTGATT	23077
rs533286983	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77110054	AGTGCACCTTGAAAA[C/T]GAACAGAACAACAGC	23077
rs533293159	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77257534	TACCCATAAAATTTT[A/T]AAAAAAAATTTAAAT	23077
rs533300162	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77138875	AATTCATTCCACACA[A/G]CTGTATAAATAAGAA	23077
rs533312522	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77227999	TTACAAGTAAAAAAA[C/T]TGAGATGAGGGTCTT	23077
rs533327967	snp	A/G			intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77073642	ATCTAAGAAAACCCC[A/G]AAGAGTCTATAAAAA	23077
rs533330007	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77251099	CTCCGGAATGATTTT[A/G]CAAAGAAATGTGTTC	23077
rs533333319	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77327053	CGCCGCCACCACCGC[C/T]ACCACCGCCACCACC	23077
rs533335791	snp	C/T	0.00478085	0.0486577	intron-variant	MYCBP2	GRCh38.p7	13:77143137	AAAACAAAAGAAATA[C/T]GTTTTTCAAAGTTAA	23077
rs533355770	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77094453	GCAAACCAGTTCATG[C/T]ATTTCTCTGTTTAAA	23077
rs533361061	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77070002	CACCTGGTTATATTT[A/T]AAAATATTAACACTG	23077
rs533361324	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77078550	AAATTTTAAGATACC[A/C]TGAGTCTTTGTTGGG	23077
rs533373076	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77273989	GACTACTTGTCATAC[G/T]TATTTTACCTTTTAG	23077
rs533404445	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77127068	TATGCATTAAAAATA[C/T]AGCTATATCTTGCTA	23077
rs533415870	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77267242	GCAGTGATTTAAGTG[A/G]ATATATAAAAGCCTC	23077
rs533418370	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77327506	ATCCCAATTAGAAGT[A/G]CCTTTAGCGATCTTA	23077
rs533430443	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77318788	AAACTTCAATTACTT[C/G]ATAATATGACATGTG	23077
rs533448544	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77172688	AGGTGTAAAGTATGA[A/G]GGAAAGAGAAGTCCA	23077
rs533462543	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77107630	CCAGTCCTCACTACT[C/T]AGGAGGCAGAGGTGG	23077
rs533472847	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77135302	AAAGTTCATTTACTT[C/T]AAACGAACTGAAGTA	23077
rs533474805	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77143729	CATTGTGCAAACATC[A/G]GAGTGGACTTAAGCA	23077
rs533491956	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77194300	ATACATATCTGATGA[A/G]CAATGTGTTCATAAT	23077
rs533494231	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77070749	AAAAAAAAGAATGAA[A/G]TGGTCTCTTTAAATA	23077
rs533499861	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77104767	AAAAGTCACAGACTG[A/T]CTACAGCAGTTTCCG	23077
rs533500643	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77086571	TTCTGAAACTCCAAG[G/T]AGGTAAGTTGTACAT	23077
rs533501376	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77161843	GACAAATAGGCTGAT[C/G]TGAGTGACAATACTT	23077
rs533515616	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77296075	AATAAGAATAAATAG[C/T]AAATAATTTTCAACA	23077
rs533534283	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77094199	AATGGAACTGTTGGT[C/T]GGCAAGCCATGTCAG	23077
rs533542671	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77134540	TGCTGTAAAAACAAA[C/T]AAACAAACAAAAAAC	23077
rs533543050	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77281034	CAGACATGTTCTTAA[A/T]TAAGTCTTTTTCTGC	23077
rs533549337	in-del	-/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77257884	CCCTTCTGAGCCTAG[-/T]TAAAAGAACTACCTC	23077
rs533552998	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77127892	ATTTTGTGAATCTCA[C/T]TATAGTGATGAATAA	23077
rs533557223	snp	A/G	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77316684	ACAGACGGTAAAATT[A/G]ATATCAACAACTCTT	23077
rs533565580	snp	A/C	0.00557542	0.0525036	intron-variant	MYCBP2	GRCh38.p7	13:77264299	TGCACCACGATGAAC[A/C]AACTATAATGTTGGT	23077
rs533567318	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77052125	ATAAAGCTATTTCTT[C/T]TTTTTCTTTCTTCCC	23077
rs533590750	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77108638	GAGAAAGAGACAACG[C/T]TTACGCAGCACAAAG	23077
rs533611912	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77236489	CCTAGGAATCTATCC[C/T]AAAGAAAACTCTAAA	23077
rs533612390	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77136098	TGCTGGCATAATAGG[C/T]GTGAGCCACCGTGCC	23077
rs533622353	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77274807	AAACCAAAAATCTGA[C/T]TGTCTACTTAAAATT	23077
rs533622729	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77156718	TCCTCATTACCTTGC[C/T]TTCCACCTAAAATGC	23077
rs533659826	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77063162	AGATAATAAAAGTTC[C/T]TCAGAAGTCTTTGTT	23077
rs533682961	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77118998	AACATAGCAATGTGT[G/T]TACATTATAGTTATA	23077
rs533683679	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77257061	TAACCATAAAAAACA[C/T]TGAGATCCTATCATT	23077
rs533708287	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77172106	GGGTTTCACCACGTT[C/G]GCCAGGCTGGTCTCA	23077
rs533712032	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77274230	AAATTGAGATATGTG[G/T]TATCAAAAGATTTTT	23077
rs533714692	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77152531	AATGTTGCCTTTTTG[A/G]CCAGCCCTGCCCCCC	23077
rs533743133	snp	C/T			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77292676	AGAGGGTAAGAAAAC[C/T]GGCCAGGCACGGTGG	23077
rs533753460	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77150134	AAAATATATATTTTT[A/T]AAATGTCTAAAGGTA	23077
rs533755072	snp	A/C	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77302302	AGAAAATCTTTAAAG[A/C]AGCCAGAGAAGAGAT	23077
rs533768153	in-del	-/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77212399	ATTTTTTAAAAAAAA[-/G]TTTGAAATATTTTCC	23077
rs533787680	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77242199	GCTCACTGCAAGCTC[C/T]ACCTGCCAGGTTCAA	23077
rs533788228	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77162918	CCTTGGCCTCACAAA[A/G]TGCTGGGATTACAGG	23077
rs533788538	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77236945	AAACACTACTCTTAT[A/T]CATTAGTCTAGGGAG	23077
rs533816632	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77279949	GGAACATGTCTTAAA[C/T]GGCTTGTATTATCTT	23077
rs533823153	snp	C/T	0.000148499	0.00861553	missense	MYCBP2	GRCh38.p7	13:77093264	GGTACAGATGTTGAA[C/T]GTAGATATCTCATTT	23077
rs533825109	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77101643	GGTGACAGCTAAATA[C/T]CTGTTGAAGTTTAGG	23077
rs533846546	snp	C/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77187394	TGGCTCTTTTGGAAG[C/G]TCAACTTTGAGAGGA	23077
rs533854270	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77287136	TCGTGATCCGCCCGC[C/T]TTGGCCTCCCAAAGA	23077
rs533874256	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77295414	GGGGATTACAGGCGT[A/G]AGCCACTGCACCCAG	23077
rs533883425	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77257584	AGAGCCACTCATTTT[A/G]AAAAGAACAAGACTT	23077
rs533888288	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77100445	AGTAATATATTCCAA[C/T]TTTCTTGATTTTTTT	23077
rs533893515	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77210796	AACAGAACTCTCAAC[A/T]GTAAAATTAATAATT	23077
rs533910259	snp	A/C	0.000399281	0.0141238	missense, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326553	TCCTCCGGTAGCGGT[A/C]GGCCAGGGCCCGGCC	23077
rs533916213	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77179925	TTTATATTCCTGTGG[A/G]TGCTGGGTAAACTGG	23077
rs533917371	snp	A/G	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77310098	GCCTGGCAACGGAGT[A/G]AGACTCCGTCTCAGA	23077
rs533931205	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77170943	CAACTAGATGGAGAA[C/T]GGGGGAAAGGCAGCA	23077
rs533937089	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77271382	ATCTTGCAGTACTAC[C/T]ATGTCTACCCTGCTT	23077
rs533937631	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77069614	GTAATCCCAGCACTT[C/T]GGGAGGCCGAGGCGG	23077
rs533943117	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77218844	GAGAGCTCTGCTTTT[C/G]AGAAATGTAATTATG	23077
rs533944760	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77242375	TGCCTCAGCTTCCCA[A/G]AGTGCTGGGATTACA	23077
rs533946929	snp	A/G			synonymous-codon, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77078836	TACCTGCTTTATTCT[A/G]CACAAATCTTCTACT	23077
rs533947527	snp	A/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77225965	AGTACTAGCCATTTT[A/T]AAAAAATTGCTAATG	23077
rs533955799	in-del	-/TTAAG			intron-variant	MYCBP2	GRCh38.p7	13:77132176	TTTACTAATGTTGTA[-/TTAAG]TTAATATTATTGAGA	23077
rs533969639	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77238645	CTAAAAAGATAAATT[A/T]AAAAAATTAACTAGA	23077
rs533974515	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77135406	ATTTAGGTGTGTTAT[C/T]TCCTTGAGAAGATGA	23077
rs533985338	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77261104	AAACTTTATCTTAAT[A/T]AAGTTTTATTTTTAC	23077
rs533988999	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77111158	ATGAGAATGCTTTAA[C/T]AATATTTTTTAATAA	23077
rs533990427	snp	A/C	0.00438332	0.0466095	intron-variant	MYCBP2	GRCh38.p7	13:77195630	CATTTTTCCATATTT[A/C]TCTGCCATTACTGTA	23077
rs533994056	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77327086	CGGGGCTACCCGCAA[C/T]GGGAAGCTGCCGGCC	23077
rs533994379	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77117830	CTATCATGAATGAAG[A/G]ACTAGAGCAATCCTA	23077
rs533995858	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77318392	GAATTCATGTCCTAA[C/T]AAATGAGTAGACATT	23077
rs534006321	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77062153	TGGTGAAAGGGCCTA[C/T]ATAAAGTTTTCCTTT	23077
rs534024025	snp	G/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77202165	TAATAAAGAAAAAAA[G/T]AGAGAAGAATCAAAT	23077
rs534066413	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77070261	AGGACCTATAAAAGG[G/T]CGAGCATAAAAAAGC	23077
rs534066792	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77287638	ATATCAAGAGTACAA[C/T]TATAAGCTTAGGCAG	23077
rs534073406	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77242915	CCCTGAATATTTTCC[C/T]ATTATATGAGTTATC	23077
rs534083508	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77134888	AAAGTTCATACTTAA[C/T]GATGAATACACGAAT	23077
rs534084540	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77054995	ATTTGTAACTAAATC[G/T]CAAAAATTTTGGGGG	23077
rs534085064	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77212471	TTAAATGAAAAGTAC[A/G]ACAAATACACACAAT	23077
rs534108479	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77110930	ACTTGAAATTATGCC[A/G]TCATAAGACATAACG	23077
rs534125379	in-del	-/CACAC	0.00159744	0.0282165	intron-variant	MYCBP2	GRCh38.p7	13:77245746	CAGAACGTAAAGTAA[-/CACAC]ACACACACACACACA	23077
rs534130263	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77318973	TGTGGCATGAGCTAA[C/T]GTCAAAACCGTGAAC	23077
rs534134738	snp	A/T	3.30442e-05	0.0040646	intron-variant	MYCBP2	GRCh38.p7	13:77165262	AGAATGAAAAGATAA[A/T]TCATTCTTACCTCAT	23077
rs534140504	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77048197	GTGCTCTTCCTATCA[A/G]TGAGACCCAGGAGAG	23077
rs534148956	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77258769	AGTACTAGCTGACAT[A/G]CTTTGAGACCTTACA	23077
rs534150657	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77178678	GGGAGACTAAATAGA[C/T]ACAAAAATGGAAGTT	23077
rs534156665	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77127258	AAAGGAGAAATTAAA[A/C]ATGGATTTAAGTAAA	23077
rs534159968	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77247025	ATAATGGTGAGAGAC[C/T]GAAAGCTTTTCCTCG	23077
rs534169029	snp	A/C/T	3.29692e-05	0.00406001	missense	MYCBP2	GRCh38.p7	13:77212064	TTGCACCTATCCAAG[A/C/T]AGCTTTTCTTCCATA	23077
rs534174996	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77095282	GTGTAGGTCAAATAC[C/T]GAACTACCCTAGATA	23077
rs534178491	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77300401	GAGAGGAGTGTGCAT[A/G]TATTACAATAAAACT	23077
rs534183936	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77280447	AAGTCAAAGATCTCC[A/G]GAGTACAAAATATGG	23077
rs534211472	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77126009	TCCATACCGATCACA[C/T]AGAATATTTTAAGTG	23077
rs534237088	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77094837	ACATACTTCTATTGT[A/T]GCACTCCTCACATGG	23077
rs534237762	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77103679	TTTTTTAATAGTGGA[A/G]GATAAAGAAATGTTA	23077
rs534241512	snp	A/G	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77205102	GTATTCGATTTTAGC[A/G]ATGTTTTCTCTATCG	23077
rs534247555	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77266455	TAGATTAAAAAAGCA[A/G]TATGTAGCATATGAT	23077
rs534265108	snp	A/C/T	0.00115783	0.0240331	intron-variant	MYCBP2	GRCh38.p7	13:77164545	TTGGATGACTCCCTA[A/C/T]GGAATTGCATAAAAT	23077
rs534282952	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77219129	AGATCCTAATTTCCC[C/T]TATGAGTCTCTTCTA	23077
rs534290138	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77105764	TCACTAAGTTTAAGA[A/G]AATAATATTAAAAAC	23077
rs534300590	snp	A/G	0.000829141	0.0203441	intron-variant, synonymous-codon	MYCBP2	GRCh38.p7	13:77118377	GGAAAGGGGCTGTCC[A/G]AACACAAATGGGCTG	23077
rs534301361	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77183404	ATAATTTTTAAATGG[A/T]TATGAGGCAATTCAG	23077
rs534323751	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77136210	ACTTCTTAGTTCCTA[C/G]ACTTAGGCACTTGTA	23077
rs534358962	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77218057	TAGGAAAGATAAAAG[G/T]CACTCATAAGAATAT	23077
rs534383605	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77321433	TACACATACAGATTC[A/G]ATCCCGCATTACTTC	23077
rs534387546	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77181474	GTGTGTGATTAAACC[G/T]TTAGAGCAAAAAAAC	23077
rs534389189	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77308986	TTCTTTTCAGGCAGA[C/T]AGTCATAGATGTTTG	23077
rs534395927	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77311731	ACCTCATCTGAAAAA[C/G]AGAGAAAAAAAATTG	23077
rs534396549	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77157653	TACCTGGGAGGCTGA[A/G]GCACAAGAATCGCTT	23077
rs534397552	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77222298	ATTCTGCCAAACACA[C/T]CTTTTGCTCTTTGCA	23077
rs534418866	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77267399	CCTTTAACATAAAAT[A/G]AAATAAAATAAAATT	23077
rs534442229	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77110369	TCAGAAGGCGGGGAA[A/C]AAACCCCACCCTGGT	23077
rs534451364	snp	C/G	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77065657	GAGAATGAGAAACTT[C/G]CACTTTCGAGAGCTC	23077
rs534469448	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77050694	TTTAAATGGTTCTGT[A/T]ATATTGAACTTCATA	23077
rs534472139	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77215085	TGGGGAGGCAGGAAT[A/G]TCAAGGATATGGGAG	23077
rs534487940	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77106859	CACCCAGGTAATCAA[A/G]CATTACCTGACAGTT	23077
rs534501215	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77251517	ATTTTAATTTAGGGA[C/G]CACTAATAAACACTC	23077
rs534531496	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77057499	GGCAAAAGTTAAAAA[A/G]ACCTATTTAGTGCAC	23077
rs534540540	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77303902	CCAATGAAATGGAAA[A/G]CAGACATTCAATAGA	23077
rs534560001	snp	C/G	1.65034e-05	0.00287253	missense	MYCBP2	GRCh38.p7	13:77098930	GTCCATCAGGTTTAA[C/G]CGATCTGCTGTGTTT	23077
rs534561838	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77113645	TGTCTTGTAAGCAAC[A/G]TCAGCATTCTTTGTG	23077
rs534568368	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77255408	TTACTTTGATTATTA[C/T]AAAATGTCACTGAAG	23077
rs534617521	snp	C/T	4.95111e-05	0.00497525	synonymous-codon	MYCBP2	GRCh38.p7	13:77098148	AAGAAAACTCGATTT[C/T]TCTTTTTTGGGCCTG	23077
rs534619401	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77107535	TGAGCCCAGGAGTTT[C/G]AGACCAGCTTAGGCA	23077
rs534620291	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77230529	TGGAATATTTGCATA[C/T]ACATTATGAGATATC	23077
rs534629949	in-del	-/CT	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77104106	CTGAATTTAAAAAAA[-/CT]CACTGTATTTAAAGT	23077
rs534636281	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77209207	CCATTGCTACTACCA[C/T]AAATGGAAAAGACAA	23077
rs534638375	snp	A/C	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77307640	CAAAAAAAAAAAAAA[A/C]AAAAAAAAAAAAAAC	23077
rs534641880	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77139116	GGGTTACCTCAGAAC[C/T]GAAAAGCCTTAATTA	23077
rs534652137	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77262684	CTCCATCAATTCAAA[C/T]ATATATATATGTAAA	23077
rs534665277	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77269613	CCTGGGTGACACAGC[A/G]AGATTCTGTCTCAAT	23077
rs534715376	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77247314	CTAGACACTAACAAT[C/G]AACAATATGAAAAGG	23077
rs534730342	snp	A/C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77147150	AAACTTCTGGAAAAC[A/C/G]TATTGAACAACCCAA	23077
rs534740096	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77199767	TAACTGGGAGGCACC[C/T]CACAGCAGGGGCAGA	23077
rs534753385	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77198091	GTCAAATAGAACTAC[A/G]TAACACATTGAGGTT	23077
rs534772688	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77208270	TCCTCAACCTTGGAA[A/G]AATAAACTTCTAAAG	23077
rs534786455	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77240175	AAAGATAAAATCATA[A/G]AAGTGTCATATCAGA	23077
rs534788892	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77270126	ATCAATGAAAAATAA[C/T]ACAAATGGGTGAATG	23077
rs534790285	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77131715	TGCATGTGTATATAC[A/G]AACACACATATATAT	23077
rs534798580	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77163010	AACTTGCTTTTCTCA[A/G]TATAATTTGGACAGC	23077
rs534816639	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77160719	CTATTACTAACTACA[C/T]ATACCTAGTATAGAA	23077
rs534818413	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77306929	TTAAAGAAATAAAAG[A/C]CTATCATTAAAATAT	23077
rs534822223	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77314277	TGTCAATTTCTAAAA[A/G]AGAAAATGTATGTCC	23077
rs534822471	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77168738	TGGTTACTCTAATAA[C/T]AATTTCCATCTAAAT	23077
rs534840527	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77261992	TAAACTAATCAACAG[A/G]TTGTATTTTAATCTC	23077
rs534865795	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77222945	TACACTGTGACTGCG[A/G]GGAAGAATAAGGCAG	23077
rs534875088	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77224150	TATTGCCATGCACAG[A/C]CTTTAAAAAGATAAT	23077
rs534882192	snp	C/T			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228587	CAAAGCTTAGATCTA[C/T]ATAAAAAATTAAACA	23077
rs534890695	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77278392	GTGCACGAACTTCAA[C/T]TCTTAAACCATAACT	23077
rs534900310	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77314504	ACATTACTAAGTGAA[A/G]GAAACCAATCTGAAA	23077
rs534905485	snp	C/G/T	5.07535e-05	0.00503732	intron-variant	MYCBP2	GRCh38.p7	13:77051183	GCAAAAGAGAAGAGA[C/G/T]AGACACAAGATCATA	23077
rs534912929	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77233484	ATAATTTATAAAGTA[C/T]AAAACCCGTCTTGTA	23077
rs534938625	in-del	-/CAA			intron-variant	MYCBP2	GRCh38.p7	13:77256633	ATATGAAAAGGTGCT[-/CAA]CATCATGGATCATCA	23077
rs534955536	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77254865	TTGTCTCTGTCCCTG[A/G]TTTATTTTATTGCAG	23077
rs534958588	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77153598	ATGAACCTTGAAGTA[A/G]ATCACTGAATAATTT	23077
rs534968972	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77300552	ATTGGTCTGTGGGTC[C/T]TTGTTTGCTCGCCCC	23077
rs534996404	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77125100	TTAAAAGCCTGTTTT[A/T]TAAAGATGAGTCTAT	23077
rs535002054	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77142316	CCCAGGAAAATGTAT[A/G]CTCAGAACCAAAAAA	23077
rs535011958	snp	C/T	0.00835141	0.0640778	intron-variant	MYCBP2	GRCh38.p7	13:77200262	AGAAGCCTCAGGAGC[C/T]GATGAGATCAACTGG	23077
rs535014763	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291881	CCAAGGAAACCATGA[C/T]TGACCCTTGGCTAAC	23077
rs535019331	snp	C/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77115682	GTAAAAACTATGATT[C/T]GGAAAAAAAAAACCA	23077
rs535034226	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77271174	CAAATAATTTCAATA[C/T]CTAAGGACTTGGCAG	23077
rs535037224	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77169327	CGTGAACCCGGAAGG[C/T]GGAGCTTGCAGTGAG	23077
rs535039231	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77169168	AATCCCAGCACTTTG[G/T]GAGGGCGAGGCGGGC	23077
rs535056789	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77284164	ATAATTTAAAACTCA[A/G]GAATGGGAAAAATAA	23077
rs535060983	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77223183	TTGGATGCACGAGGA[C/T]ATTCGTCCCCTGGGG	23077
rs535089493	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77277549	CTGACATGTAGTTAG[A/G]TTCATGCAGTTTGGT	23077
rs535116929	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77140788	CTGGCCATTTTGAAG[A/C]ATCAGTGACAAACGT	23077
rs535133178	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77149974	GTTACAAAACACAAA[C/T]CTAATCAAGCCATTC	23077
rs535135735	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77210729	TATGAGAACAAAAAA[C/T]AGAATGAATTCTATA	23077
rs535148899	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77314821	AAATGCCACTCTGGT[A/G]GGGGATGTTGATATG	23077
rs535149376	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77092208	TTTAATAAGCACATT[C/G]TCTTTTCATTCAGCA	23077
rs535163092	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77292580	TATATGAAGTTCTAG[A/G]AAATGAAAACTAATC	23077
rs535207420	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77286146	TTAAGGATGGTGGTG[G/T]ACTTAGGAACAGCCA	23077
rs535211331	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77248323	ATCAACAGAGTAAAA[A/G]CACAACCCACAGACA	23077
rs535223136	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77168861	TATTTTTAAAAACTT[A/G]TTTTTTCATGATCTG	23077
rs535242061	snp	G/T	1.76558e-05	0.00297113	intron-variant	MYCBP2	GRCh38.p7	13:77270287	AGGAACTGTAAGGAA[G/T]CACATTACCCTAACT	23077
rs535260066	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77199808	ACACTGCCTGGTACT[A/C]CAACAGACCTGCAGC	23077
rs535288587	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77308525	GAAAACAGTACCTCT[A/C]CCACTGGATGATGTC	23077
rs535295365	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77271090	TCTCACTACTTAATC[A/G]TACTTTTGATATTTT	23077
rs535295558	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77209270	TCTGTTAAGACCCCA[C/T]GGAAATGGTTCTAGT	23077
rs535307598	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77051250	ACATAGACAGCTCCT[A/T]AATTCATATTTTGAG	23077
rs535324710	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77149316	TTTGAATCACTGCAT[A/G]TTTGTTTCAGGTAAA	23077
rs535330775	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77201101	ACACAGACTGGCACA[C/T]TGGGTAAAGAGTCAA	23077
rs535342755	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77315139	TAACTATTAAAGAAC[A/G]TGAATTTGTCAAAAG	23077
rs535364400	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77200286	CAACTGGAAGAAAGG[C/G]TATCAGCGATGGAAG	23077
rs535391362	snp	G/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77214953	TACATACATATATAG[G/T]TATATATATATAAAA	23077
rs535406665	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77123315	TTTATGTCTGTATCT[A/G]TACATCAAGAGTAAA	23077
rs535417117	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77184980	ATAAGTCATGTACAC[C/T]GAATGATTTCCTAAT	23077
rs535418045	snp	A/G			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77086855	AAACTAAAAATATCA[A/G]TTATACTTAGATTAG	23077
rs535429531	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77154577	AAAGAAAATACAACT[A/G]AAGAAATATCAGAAG	23077
rs535436484	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77074890	AAAGGAACATGAGAG[A/G]AATTTGGGGAGTGAT	23077
rs535437077	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77132863	ACTTGCATTGTCCCT[C/G]ATATTTGAAACATTC	23077
rs535454068	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77083670	TACGCAAATGGACCA[C/T]AGCTAGGAAAGAGAA	23077
rs535455475	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77213768	GACGTCAAATCTTAT[C/T]ACTCACATAACCACC	23077
rs535455812	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77093095	GAACTTCTACAGGAC[C/T]CTTTTCTAGTTCAAA	23077
rs535457031	snp	C/T	1.69043e-05	0.00290721	missense	MYCBP2	GRCh38.p7	13:77185375	CAACTGCTTTTCCTG[C/T]AGCTTTGAGGGGGAA	23077
rs535474326	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77222539	ACCCTGCCTCAGCTC[A/G]AAGGGTAGAGAGTGG	23077
rs535485093	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77232517	AACCCAGAACTCTGA[C/G]ATCTCAAAGGACAAC	23077
rs535499835	snp	A/G	1.658e-05	0.00287919	intron-variant	MYCBP2	GRCh38.p7	13:77140978	ACTGTAACATTTGAG[A/G]AAAAAAGAGAAGGAA	23077
rs535548402	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77279144	TGATTGTACTCAAGG[A/G]AAATTCAGTACTCTT	23077
rs535583151	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77275482	ATTCACTCCCTCCTA[A/T]TCACCCTCTAAATCT	23077
rs535609264	snp	A/G/T	0.00239393	0.0345281	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075675	TGTTGATTTCTTTTT[A/G/T]GGGGGGGTGAGGGGA	23077
rs535609302	in-del	-/T			intron-variant	MYCBP2	GRCh38.p7	13:77059260	AATACAGTTCATAAA[-/T]TTTTAACTGTTTCTA	23077
rs535618066	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77116431	CATTTACCTTTCCCA[A/T]CACGGTATAAAAAAT	23077
rs535629287	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77217516	GAAAAATTCATCTCT[A/G]CAAGTTAGATGAGAA	23077
rs535638885	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77125740	AGAATTACCCAAGAA[C/T]ACATGGCTCATTTTC	23077
rs535641382	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77162016	TTTAGTTTAATTTTC[C/T]AGTCCTTTGCATTCA	23077
rs535647340	snp	A/T	0.000798403	0.0199641	downstream-variant-500B	MYCBP2	GRCh38.p7	13:77044397	AAATGCTGCTAGTTA[A/T]AATAGAAGTTAATTT	23077
rs535662560	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77255465	GCTCAATTTTCACAA[A/G]AGTTTCAGAATAAGG	23077
rs535669395	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77215931	ATAAATATATGCATA[C/G]CAGAGATCCAAAGAC	23077
rs535675263	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77255052	TGGATATGGCTATGA[C/T]AAACCTGAGAATGCA	23077
rs535681206	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77243034	GTGGATTTTCATGTA[C/G]TTTTTCTCTGTAGCT	23077
rs535698046	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77235016	TAAAAATTAAAGCAA[C/T]TGGGCTCGAAAATAC	23077
rs535710282	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77265495	GAATAAAATGACAAT[C/T]ATCAGATAAAAAAAG	23077
rs535722945	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77147983	GAAATATTGCATTCC[A/G]TTGTGGTAACAAAAT	23077
rs535734315	in-del	-/AA	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77206906	CATAACTGATGATAC[-/AA]AGAGAATAAATAATA	23077
rs535747369	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77256904	CCAAAAGAAAGGAAA[C/T]TAGTACATCAAAGAG	23077
rs535765286	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77099654	CAGGTTACACTCCAA[A/C]AGTTCAGGAAGCTTA	23077
rs535773424	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77309399	AGAATCCTAGCAGTA[A/G]ACTTTTCAAAATACA	23077
rs535782600	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77108979	ATTACAGGCATGAGC[C/T]ACTGTGCCCAGCCAG	23077
rs535792980	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77264402	TGTCACAGAAAAATA[C/T]GACCTAAAGCTTCTG	23077
rs535805003	snp	A/C/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77293707	AAACAACAGAAAACT[A/C/G]TCAGTGATGCCGCAT	23077
rs535805850	in-del	-/TTC	0.00279162	0.0372561	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77086916	TTCATCACTTCATAT[-/TTC]TTCTTACAATTTCTT	23077
rs535809435	snp	G/T	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77047858	AGACAGCCCACAGAC[G/T]AAGCACATTCCTTCC	23077
rs535814264	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77069487	AATTACACCTGTAAT[A/C]CCAGCAGTTTGGGAG	23077
rs535815430	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77244496	GACCCCTTCCTTACA[C/T]CTTATACAAAAATTA	23077
rs535815715	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77236880	TCTACAAAAAATAAA[A/T]AAATAAATAAATAAA	23077
rs535852137	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77249005	CTAAGTGAAATAAGC[C/G]AGTCACAAAAAAGAC	23077
rs535862471	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77301379	CAAGAGCCAAGATCG[C/T]GCCACTGCACTCCAG	23077
rs535863205	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77149006	TTCTATTTTTATATT[C/T]GGAGTATCTTTATTG	23077
rs535868531	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77197832	GAAAGGCCTTAGCCC[A/G]CTCACTGGATAATTG	23077
rs535884659	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77247639	TGAAAAAGAAGAACA[A/T]AGTACTCGGTTTTGA	23077
rs535908865	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076242	ATTAGACATGGACTT[G/T]GTCTTTAAGAAGCTA	23077
rs535920022	snp	A/T			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77227811	CAATAGAGACATAGC[A/T]TCAAGGAAGGAGATT	23077
rs535921098	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77286977	GCAAGCTCCGCCTCC[C/T]GGGTTCACGCCATTC	23077
rs535927088	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77178053	TAACCTTTATTTAAT[A/G]AGTGGATATAAACAT	23077
rs535934386	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77079814	CATATCTGTGTTCAA[A/G]AAGTTTCAGATTCTG	23077
rs535937989	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77063323	AGCACTTTGGGAGGC[C/T]AAGGTGGGTGGATCA	23077
rs535953873	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77137435	ATAACATTTTATTAG[A/G]GACTTAAGAAAATTT	23077
rs535957855	snp	A/C			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77078549	TAAATTTTAAGATAC[A/C]CTGAGTCTTTGTTGG	23077
rs535960265	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77286277	TTCAAGGCATAATTT[C/T]AAGGTATCAGTTTAG	23077
rs535965977	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77319242	AGAGAGGAGGAGCTG[C/G]GGGTAAGAGGGACAG	23077
rs535967013	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77088407	CAGATTTACTATATA[C/T]AGGCCTGTAATATAC	23077
rs535983701	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77186234	TTTATAGTTCATTTA[C/T]TAAATTACCCTCAAC	23077
rs535986399	in-del	-/TTTG	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77062511	TATGTTGATGTGTTT[-/TTTG]TTTGTTTGTTTGTTT	23077
rs535993765	snp	C/T	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77110776	TAGAAAGAACCTACG[C/T]TGAAATATTGGGGGC	23077
rs536001728	in-del	-/CAGA	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77074819	GCAACACAACACTGG[-/CAGA]ATATAGTTCAGTAGT	23077
rs536005958	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77129995	TTTTGTTAAGGAACA[A/G]TTAATTCACAGAAAC	23077
rs536014108	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77278349	TTTTGTTTGCCCCCC[A/G]CTTCATCATACTAAT	23077
rs536029118	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77279682	GGAAGAATATTCTCT[C/T]TGCTGATATTTTTGC	23077
rs536033908	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77325565	GAAGGTGTAGCCAAC[A/C]CAAGTAAAAGAGACA	23077
rs536045003	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77178779	ACTCCCAAAGTTGTA[C/T]ACCAGGCACCCTGTA	23077
rs536063880	snp	A/G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77124998	GGTAGTTGGAATACC[A/G/T]AAGTTTCATTTTATT	23077
rs536064076	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77295766	TCAGTATAAAAAAGA[C/T]GGATTTTATAGAGAT	23077
rs536099523	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77268709	GCCTGAACCTGGGAG[A/G]CGGAGGTTGCAGTGA	23077
rs536109342	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77163722	CTTCCTTACTTTCCA[C/T]TCTCCCTCTCTACTC	23077
rs536137455	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77052631	CTATGCTTTTTTCAG[A/G]GTAAAGTTTGAGAAA	23077
rs536196534	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77136518	CAGCAGCTCAGCAAC[C/T]AGTACTATAATTTGC	23077
rs536197193	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77060315	AAAAGGATGGTTTAC[A/G]AGGATGGTTTGACAT	23077
rs536198729	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77275842	TACAAAAATTAGCCG[A/G]GCATTGTGGAACGCG	23077
rs536203615	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77156857	AAAACGTCTGCATAG[C/T]ATAGTAGTGAGGCTG	23077
rs536209481	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77297489	GGAATGCAGGGAGAA[C/T]GAAGGGGAGGAGGTT	23077
rs536216227	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77118045	TACCCACTGATAAGA[A/G]TGAAATGGCTTTATC	23077
rs536244172	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77263292	TAATAACATTTACAA[A/C]GTAAGTTTTCAAATT	23077
rs536249890	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77288570	TTTTTGAGCAATGCA[C/G]CAATAACCAACCAAT	23077
rs536250197	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77233580	TCAATCAAATTATCT[C/T]ACAAATACTTTTTTA	23077
rs536253335	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77159888	TTGCCTGACACATAT[C/T]GTTTATTATATATCT	23077
rs536254798	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77114735	GCTGGAAGATGTCTA[A/C]TATGTACCCATCAAA	23077
rs536261412	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77144053	ATGCATTCATTCATC[A/C]ATATTTGCTGTCATT	23077
rs536270611	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77296489	GCTTTTACAAAATTA[C/T]TTCAGCACATACTAA	23077
rs536271154	snp	C/G	0.000150184	0.00866426	intron-variant	MYCBP2	GRCh38.p7	13:77261130	TTTACTAAAATAAAG[C/G]ATTTATTTTTATTAA	23077
rs536279799	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77197423	ATGGTGGATGGTACT[A/T]ATCATGAGAGAGAGA	23077
rs536314189	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77071473	GAGAATGTCCCTTTC[A/G]CCCTAACAATGAGGA	23077
rs536325546	snp	A/G	3.30677e-05	0.00406605	missense	MYCBP2	GRCh38.p7	13:77181733	TATGTGCCACCAAAA[A/G]GGGAAAACGATGAAC	23077
rs536328163	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77145569	TATTTCCAGCCTATA[C/T]ATAATTCTGCTATCT	23077
rs536341415	in-del	-/ATATA	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77112351	TAATATATATTTTAT[-/ATATA]ATATTTTATTTATAT	23077
rs536349409	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77287630	AAACCACAATATCAA[G/T]AGTACAATTATAAGC	23077
rs536362174	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77289413	CAATGCTGGCACAAC[A/C]CTGGAAAAGCAACCA	23077
rs536362600	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77180801	GGTATGTGCCTACAG[C/T]CCCAGCTACTTGGGA	23077
rs536376290	snp	C/T			intron-variant, nc-transcript-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075549	ATATCCCCTAAGAAG[C/T]CTTCTCTGACCACTC	23077
rs536377350	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77298514	GTTCCTGGGATATAG[C/T]ACTCAACGAGTATTT	23077
rs536391056	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77152881	CCATCCTGGCTAACA[C/G]GGTGAAACCCCGTCT	23077
rs536397061	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77148491	TCTACTTTGACGTCT[A/G]GTCCCTCTTACTTCC	23077
rs536429361	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77275247	TATTCTTCATGTAAT[A/G]AAATAGAGAATGACT	23077
rs536430516	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77217264	GTATTAGCACAGTCT[C/T]GCAAAGATTTTTCTT	23077
rs536434678	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77319958	GTTTATTGCGGAGTG[C/T]CCTCCGAACCAACAA	23077
rs536460011	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77142042	GTGGATTTTTCTTAT[C/G]TAATTTGTATCAGTT	23077
rs536467049	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77146361	AATTACCTACTTTAG[A/T]CCATTTATTAAAGAT	23077
rs536468535	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77203536	TCTTCACAGAATTGG[A/C]AAAAACTACTTTAAA	23077
rs536498672	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77328004	AATATACGTGCCAAT[A/G]CACTTTGATTCCTAC	23077
rs536512083	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77159383	CAATTTGGGACACCA[G/T]TTTTTTTTTTCTTGA	23077
rs536516905	snp	G/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77284516	AAATATCACCTGAAA[G/T]TTTCACTCCCCACCC	23077
rs536532319	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77130732	GGTCAATGGGTTTTT[C/T]TCCCTTACAAAGCAT	23077
rs536567705	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77213401	AATTGCTTGAATCTG[A/G]GAGCCGGAGGTTTCA	23077
rs536570376	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77071921	AGAAATTAATAATAT[A/G]AAGCTAACAGGAAAA	23077
rs536592333	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77072765	ATAAATCCAGAAACT[A/T]AGATGAAATGGACAA	23077
rs536597425	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77168951	CTCTTGAATATGTCA[C/G]TATTTTAAAACACTC	23077
rs536632310	snp	A/T	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77316769	AGGTGGCTGACTTCA[A/T]GGGGTGGTCACTGGG	23077
rs536639253	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77206927	AATAAATAATATAGT[C/T]AGCTTAAAGAGGACA	23077
rs536639487	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77314106	TTGGTGATTTCCTAC[A/G]AAAACTAAACCTACT	23077
rs536642085	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77306315	AATGAATAAATTAGG[A/G]AGGAATAGTTATCTC	23077
rs536646844	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77129660	CAATTATCATTATGA[A/G]TAATAATGGCATGTA	23077
rs536649885	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77079897	CCTGTTAAAAGGAAA[A/G]TAGATGTCAGCTTAC	23077
rs536649938	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77089534	AAGTGATCTCTCTGA[G/T]AATTGATCACTATAT	23077
rs536657418	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77313848	AAAGATGGGGCAAAG[A/G]CCTTAACAGACACCT	23077
rs536674145	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77213990	GAAGGAGGACAGAGG[C/T]GTGTGAAGAAGTTAG	23077
rs536696450	snp	C/T	0.000399281	0.0141238	synonymous-codon	MYCBP2	GRCh38.p7	13:77097707	AGACTTAGACTTCAT[C/T]GTGTTATGCATGGAC	23077
rs536696696	snp	A/T	0.00557542	0.0525036	intron-variant	MYCBP2	GRCh38.p7	13:77089664	TTTTTTTTTTTTTTT[A/T]AATCGATTAAGGGCT	23077
rs536699907	snp	A/C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77105057	AATTCTTCAAGACAC[A/C/G]AACTAGAACGGTGGC	23077
rs536738715	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77130047	TCTTCACAAAATGTT[C/T]TACTGATAATTTAAA	23077
rs536765128	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77208148	TTTTTCTTTTCCTTT[G/T]CTCCTCCTGCTCTCT	23077
rs536785477	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77253674	GAATACAATCAATTT[A/G]AGAAAATTCATCAAG	23077
rs536786187	snp	C/T	0.000329641	0.012834	intron-variant	MYCBP2	GRCh38.p7	13:77191646	TCTAACAAAAATAAG[C/T]ATTGCTTAAGTAACA	23077
rs536786623	snp	C/G	0.00517822	0.0506191	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77080638	TTCATGAGGACTGTG[C/G]CAAAGTAGACACTTG	23077
rs536803423	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77222196	CAATTGCAAAGCAAA[A/G]TATCAGTTGGCATCT	23077
rs536827288	snp	A/C	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77247060	ATCAGGAAGAAGACA[A/C]GGATGCTCACTTTGA	23077
rs536827896	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77188318	AATAAATCACATTCA[A/G]ATGGTGCCTTACAGT	23077
rs536830389	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77090649	ACACATGAAAACCTA[A/G]TAAAACAGGAAGCAA	23077
rs536860986	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77065585	CACCATCTTAAGACA[A/G]AGGGTATATGACATT	23077
rs536865936	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77138588	ACGAAGTGTGGGTTA[C/T]TATTATACTTCATGA	23077
rs536879542	in-del	-/A	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77233544	TAGTCTCAAATAGAT[-/A]ATCAAGAAGTTCAAT	23077
rs536885188	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77230972	AAGTAAAAGCAGTGA[A/C]TGGAGAGATAATTAA	23077
rs536899192	in-del	-/T	0.0126979	0.078662	intron-variant	MYCBP2	GRCh38.p7	13:77056099	CACGCTCTGTGTTTG[-/T]GTGTGTGTGTGTGTG	23077
rs536906306	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77236145	CAGATAGGCAAAGAA[A/G]AGAAGCCTCAGCTAA	23077
rs536914887	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77082670	GCTCTGTTTTCCCCA[A/C]GATTCTTTTCAAGTC	23077
rs536923314	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77276870	TAAGTTGCCCAGACT[C/G]GTCCCAAACTCCCAG	23077
rs536925753	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77184158	TTTAAGCAATGCTTT[A/G]GCTAAATCCCACAAA	23077
rs536952934	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77113561	TAGCAAACAAAGAGG[C/T]GGGGGAAGAGGGAGA	23077
rs536955277	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77106347	TGATTTCTTACTATG[C/T]TCTATAATCAAGCTG	23077
rs536959174	snp	A/T	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77214467	AAAAAAAAAATGAAG[A/T]GCTTTATGAATTGAT	23077
rs536963750	snp	A/G	1.6817e-05	0.0028997	intron-variant	MYCBP2	GRCh38.p7	13:77062568	GTAAAGGAAAGCAAG[A/G]TAAATTCTTACAAAA	23077
rs536986337	in-del	-/TA	0.0283406	0.115616	intron-variant	MYCBP2	GRCh38.p7	13:77112289	CCCTCTTCTTTATAT[-/TA]TATATATATATAAAA	23077
rs536987759	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77269575	AGGTTGCAGTGAGCC[A/G]AGACTGTGCCACTCC	23077
rs537035742	snp	C/T	4.95184e-05	0.00497562	missense	MYCBP2	GRCh38.p7	13:77097733	TGGACATTTCAAAAG[C/T]GGTCTCGGTTTTCCC	23077
rs537062196	snp	C/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77237811	TATGCTGATCTATTT[C/T]TTCTTACTTATACTC	23077
rs537071786	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77289526	TAGAAAAAAAAAAAG[G/T]CTAAGTTAGGAATAG	23077
rs537089993	in-del	-/A	0.00597247	0.0543191	intron-variant	MYCBP2	GRCh38.p7	13:77060315	AAAAGGATGGTTTAC[-/A]AGGATGGTTTGACAT	23077
rs537094011	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77106795	ATGTGTAGGTTTGTT[A/T]CATGGGTAAACTGTG	23077
rs537095622	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77173960	TCTGAGTACAGTCTA[C/T]CTGATCATTAGTTTG	23077
rs537107200	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77328963	GTGTCTGTTCAACCA[C/T]CACAGGCTCCTAGCA	23077
rs537111904	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77283773	GTGGTGGCAAACACC[C/T]GTAGTCCCAGCTACA	23077
rs537117201	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77275938	GCAGTGAGCCAAGAT[C/G]GCACCACTGCATTCC	23077
rs537126602	in-del	-/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77057320	TTTGGCTTCTCCTGC[-/T]TTTTAACATTCATGC	23077
rs537146856	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77283068	ACAAAGTTACTTACT[A/G]ACTGGAGTACAAAGT	23077
rs537168302	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77090849	TGGTTTTATTCAGGC[A/T]TAAGTAAACTAACAG	23077
rs537182806	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77299720	ATGATTTAGGGCTTT[A/G]TATTCTAAATCAATC	23077
rs537182930	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77072239	GAGCTTGCAGTGAGC[C/T]GAGATTGCACCACTG	23077
rs537202910	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77071511	ATCATCTACAAAACC[-/A]AAAACTTTTTTTTTG	23077
rs537230943	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77268926	AACAAATCTCACAAG[C/T]TCAGCAAGGCAGGCA	23077
rs537236829	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77284576	ATCTCATCACTTCTT[A/C]CTCTCTTTACCTCTC	23077
rs537246838	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77254683	CATTCACCCTACTCT[C/G]CTCCTGAACATTAGA	23077
rs537254729	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77317187	GAACTCCTGACTTCA[C/T]GTGATCCACTCATCT	23077
rs537257086	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77046588	ACCCAATAAATGTTG[C/G]CTATTACTACTATTA	23077
rs537275323	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291759	GGAACAAGAGCGAAA[A/C]TCTGTCTCAAAAAAA	23077
rs537282106	snp	A/G	0.00478085	0.0486577	intron-variant	MYCBP2	GRCh38.p7	13:77139868	TTTAGTCATTTTTTA[A/G]TGATAAAATAAATGA	23077
rs537299613	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77320756	ACATGCAGTACCCAG[C/T]GCCATATACAATATT	23077
rs537301845	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77247416	CTACAAAACATTGCT[C/G]AAAGAAATTAAAGAT	23077
rs537310098	snp	G/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77311570	GTTTTTTTTTGTTTT[G/T]TTTTTTTTGTTTTTT	23077
rs537312796	in-del	-/GAG			intron-variant	MYCBP2	GRCh38.p7	13:77282091	GCAGCAGCAGAAAGA[-/GAG]GAGGAGAAGGCTAAG	23077
rs537319756	snp	A/G	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77168893	AGTAAATCAGGTTTT[A/G]CTTAATTATGCCAAA	23077
rs537326163	snp	C/T	0.00438332	0.0466095	intron-variant	MYCBP2	GRCh38.p7	13:77050018	CCTCACTCTTTTTTT[C/T]TTTTAAACTGATGCG	23077
rs537350117	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77277606	AAATAGCCAAGTCGG[A/G]AAAAAAGGACCAAGT	23077
rs537351852	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77123576	TTTATGTGGTTATGA[A/C]CTATAAGGTCATTTT	23077
rs537352248	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77285363	AGTCCTCCAGCCCTA[C/T]GTCCTAACTCAACTA	23077
rs537384492	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77175909	TTGCAGTGAGCCAAG[A/G]TCACACCACTGCACT	23077
rs537391753	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77167828	AACAAGTGCACTGTA[C/G]TAGCTTGTTTACTTC	23077
rs537398194	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77066245	ATCAAACCATTACCC[A/C]AAATCCCAAGACAGC	23077
rs537398399	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77159997	CTTTTTAAAACTCAG[A/G]CGTTTCTTAACATTA	23077
rs537427253	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77166098	TCTGCTTTGCTCAAG[C/G]TAATCTTTTTTTCAC	23077
rs537435306	snp	A/G	0.00478085	0.0486577	intron-variant	MYCBP2	GRCh38.p7	13:77199234	CCTCACTCGGGAAGC[A/G]CAAGGGGTCAGGGAG	23077
rs537440449	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77302435	GGTGGGGGAAAGTAA[C/T]CTGGAATCATGTAAC	23077
rs537441111	snp	G/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77209124	TTACCAAAACATCTC[G/T]TAATCTCTGTTTTCC	23077
rs537451939	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77306820	CAAGGCACTCTGAGT[A/G]AGAACAGCAGAACTA	23077
rs537453812	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77314732	AATGTATAACCCCAA[C/G]AGTGAACCCTAATGT	23077
rs537467854	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77262447	CAAAGTTTTATTGAG[C/T]GTTTATTAGGTACCA	23077
rs537495043	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77109712	TAGCAGACTTGTTGC[A/G]GAAAGTCAGAGATCC	23077
rs537506114	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77094554	CTTGGGTGAACCAAT[C/T]ACTTTGAACGGGCTT	23077
rs537514799	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77225246	GATCTCTAGACAAGT[-/A]CCTGTTCCATCATGC	23077
rs537525313	snp	C/T	0.000399281	0.0141238	missense	MYCBP2	GRCh38.p7	13:77150811	CTAGCTTTGGTGATG[C/T]CAGCCCTCCATAAGT	23077
rs537527364	snp	A/C	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77142821	CTCAAAAAAAGTGCT[A/C]ACTGGAGCATTCTGA	23077
rs537547911	snp	A/G	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77192004	TATTTATGTTATGGT[A/G]ATAGAATTACATTTC	23077
rs537547991	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77199740	TCCCTGACCCCTGAC[C/T]CTCCAGCAGCCTAAC	23077
rs537562374	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77160268	TCACCAAACTGCCAG[C/T]GAACAAATCCCAGTG	23077
rs537573299	snp	A/C	1.64958e-05	0.00287187	missense	MYCBP2	GRCh38.p7	13:77098799	GGGGGATAATGACCT[A/C]CTGTGGGAATCTGAC	23077
rs537584442	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77258591	TACATTATTAGCTCA[C/G]ATATCACTACCTTAA	23077
rs537588412	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77150334	TTTTGTAGAGATGGG[A/G]TCTCACTACATTACT	23077
rs537637118	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77082736	TTTTCCCTCTCTCTT[C/T]TTGGGACATTTAAGT	23077
rs537666652	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77143270	AGACTGGCGTGTGAG[C/T]GTGAGTGGAGTAGGT	23077
rs537686820	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77265222	CAAAGAGAGGAGAAA[G/T]CAAAAGAAAGAGTTC	23077
rs537686953	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77295138	TTTGATTATTTTTAT[A/T]TATTTATTTATTTTT	23077
rs537702721	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77177095	AAGAATCACCCATTA[G/T]TACTCTATGACATAG	23077
rs537722045	snp	C/G			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77292938	CACTCCAGCCTGGGA[C/G]ACAGAGCAAGACTCC	23077
rs537722225	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77285422	AGCATAAGAAATTAC[A/C]ATTAGAGACCATAAT	23077
rs537724718	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77234221	CTATAGTTTCCTTGA[A/G]TTTTAACAACATCAA	23077
rs537742496	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77136256	ACTGCACTTCAGCCA[C/T]CCTCCCATGGCAATG	23077
rs537753489	snp	A/G	0.000314918	0.0125443	intron-variant	MYCBP2	GRCh38.p7	13:77288419	TTCACACTCTTTTCT[A/G]TCATCAAGTCCCATT	23077
rs537755298	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77280592	TTTTTGGCTAAGGTT[C/T]ATTTATTATAGATAC	23077
rs537778163	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77102415	TAGTTGAAAAACTTA[C/T]ACAATATGTTAGGCA	23077
rs537778863	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075051	ACATCTCTGCAGATA[C/T]ATTAAAATCAGCTGG	23077
rs537788447	snp	G/T	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77184949	GCAGATTTAAAAAAT[G/T]TTAAACTTTGCTTAT	23077
rs537791527	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77188433	TCAATTAATACATGA[A/G]AGATCAAGACCTTAA	23077
rs537814517	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77177124	AGTCCATCTCAACAT[A/T]GTGTTTCTTGAAAAA	23077
rs537825099	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77210484	GGCGTGAGCCACCGC[A/G]CCCGGCCCAGCACCA	23077
rs537833129	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77202201	CAATAAAAAATGATA[A/T]AGGGGATATCATCAC	23077
rs537833381	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77101773	ATTAAAAAAAACTAT[C/G]CTTGTTAAGTGGGGT	23077
rs537834990	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77310719	GACATCACACAGATC[C/T]AACAAACTGAAAGGA	23077
rs537836135	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77319095	CTTTGGGGTGCCTTG[G/T]TGCAGTTTGGGAACG	23077
rs537847287	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77310255	CTCCTCATTTTTATG[C/T]ACCCCGCTACCTACA	23077
rs537847452	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77318020	ACAGTGGGTCCCTTA[G/T]TCTGAAATGATCCCT	23077
rs537850989	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77245606	TACTGGGGCCTGTTG[C/G]GGGGTGGGGGCTAGG	23077
rs537863258	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77280473	TATGGGGCTCTATTC[C/T]CAAGCCAATGGAAGA	23077
rs537878485	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77210837	TAGCAAACACTTATA[C/T]GGCACCTAGTATGCA	23077
rs537904844	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77196744	AGATCATCAGAAGCA[C/T]AGTATTGAATATGTT	23077
rs537917887	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77319617	ATTTACCAAAAGCCA[G/T]CTGATGATTGTCCTC	23077
rs537936147	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77165939	AAGAAAGTGGTTTAC[A/G]AATTCTCTTACAATG	23077
rs537941350	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77195880	TCATCTCCTCCACAG[A/C]ATGATATGAAGGTTC	23077
rs537946038	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77250776	ACTCTTTATGATATC[A/G]ATAATTTTATTTAGA	23077
rs537968216	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77109874	AATTGTGAAGATTTC[A/T]TGGACATTTATCAGT	23077
rs537968776	snp	G/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77220780	TCTTGGTTGCTACTT[G/T]CCAAGTTCCACAAAA	23077
rs537976863	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77303265	TTGAACCCGAGAGGT[A/G]GCGGTTGCAGTGTGC	23077
rs537985719	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77091836	AAGCCATCCTCTTGC[C/T]TCAGCCTCCTGGATT	23077
rs537995825	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77275048	TCCTTCAGTGAGTAC[A/G]TCTGTTGATTATTCA	23077
rs537999581	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77063412	AATACAAAAAAAATT[A/G]GCCAGGTGTGGTGGT	23077
rs538006074	snp	C/T			intron-variant, downstream-variant-500B	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77088075	AAGCATGGGCTACTA[C/T]GCTTGGCACCTTGAA	23077
rs538023501	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77188000	TGCTTGAACTCAGGA[C/T]GCGGAGGTTGCAGTG	23077
rs538036864	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77086853	CAAAACTAAAAATAT[A/C]AATTATACTTAGATT	23077
rs538043365	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77206011	ATTTGAGAAAAAAGA[A/G]ACAAAGAGTTATATT	23077
rs538056515	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77159125	AATCATCTTTGGAAT[A/C]AAATAGACTTAAATT	23077
rs538064960	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77295448	ATGATATCATTTCAT[C/T]CCCGGATCCATCTGT	23077
rs538074425	snp	A/G/T	0.00104499	0.0228348	intron-variant	MYCBP2	GRCh38.p7	13:77205407	TATAAATCATAATCT[A/G/T]TGTTTTAAAAGATCC	23077
rs538098602	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77073408	TATTAAAAAGATTCA[A/C]CCCCAAAAAATCTAC	23077
rs538111446	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77088677	TATTCATAAACTTTA[C/G]AGTCTGATTTTTATA	23077
rs538114732	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77226974	AGTGTGGTTACCTAC[A/G]TTATATTTCAAAATA	23077
rs538115960	snp	A/G	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77070270	AAAAGGGCGAGCATA[A/G]AAAAGCCTTCATAAA	23077
rs538116262	snp	G/T			intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326017	GAAGGAATGTCATGG[G/T]AGAGGCGGCACGTGC	23077
rs538122978	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77236610	AAACTATAATACATC[A/T]ACTAAATGGAATAAT	23077
rs538132466	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77117134	TGCAACACAAAATTA[A/G]TAAACTAACTCCTCA	23077
rs538134522	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77127280	TTAAGTAAATATAAC[A/G]TAAATTTATTATTGA	23077
rs538150268	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77197917	GTTTGAAAAAGAAAA[A/C]TAGGGCCAATATAAA	23077
rs538174604	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77077870	TTTGAACAAAAATTA[C/T]ATAATATGTAACTTC	23077
rs538178068	snp	A/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77180008	AAGAAAAACAATGCA[A/T]TGGGGTTGCTAATCC	23077
rs538191580	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77049064	TCTTGGCTCCTATTT[A/C]TTTCCAGACCACAAC	23077
rs538196693	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77152292	AAACCCATTCTTATA[G/T]TTAAAAAATGGCAGT	23077
rs538197912	snp	G/T			intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075364	TCTCTTAAAAATCAT[G/T]TTATTTCATGGGCAC	23077
rs538207081	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77295489	AGAGCCACCAAATAA[A/G]TGCCATCCCCCAACC	23077
rs538207811	snp	A/C	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77119357	AGTATCTTTCTAGTC[A/C]TATTTCTGAAATATA	23077
rs538218674	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77274412	ACTTGAAAATCCTTA[C/T]AGAGTGAATAATCAG	23077
rs538229358	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77108708	ATAAGATACTTTATT[A/T]TTTTTTTTTTTTTGA	23077
rs538265188	snp	C/T	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77250870	TAATACAAATAAAAG[C/T]ACAGCCCCAAGTCTT	23077
rs538268724	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77275065	CTGTTGATTATTCAG[C/G]AAATATATACCGAAC	23077
rs538269737	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77259041	GAGTGTATCACTTGA[G/T]GTCAGGAGTTCGAGA	23077
rs538271206	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77118618	AACCATGCCAATTCA[G/T]AAATGAGTGAAAATT	23077
rs538282517	snp	C/T	0.00199481	0.0315187	upstream-variant-2KB, intron-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77327153	AACTGCCGCCCCTTT[C/T]CCTCCCCACCCCCTC	23077
rs538300608	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77079208	TCTGCTTGTCACTTA[C/T]GTCAGACTCTTGTTG	23077
rs538314862	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087818	CAGTGTCTCGCTCTG[C/T]CACCCAGGTTGGAGT	23077
rs538329668	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77094608	GTCCTTTAACAACCC[A/G]TGATTCCTGAAATGT	23077
rs538336795	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77243566	TGCAGTGAGCTGAGA[C/T]TGAGCTACTGTACTC	23077
rs538342601	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77298588	AAATGAGGAAGTTGA[C/G]AGCTACAGCTACATG	23077
rs538345305	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77135768	CCAAACTATTCCCAT[C/T]CCCCCATGACTTTAA	23077
rs538350861	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77111040	AAAAATGAACGTTTT[A/G]TTCAGCTTAAGTAAT	23077
rs538355666	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77144004	GGTTCTGTCTCTCTG[A/G]AGAACCCAGATTAAC	23077
rs538366670	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77124724	ATTCTTTGCTCTGTT[C/G]TGATCAGTTAAAGCA	23077
rs538375691	snp	C/T	1.65119e-05	0.00287327	intron-variant	MYCBP2	GRCh38.p7	13:77243030	GAAAGTGGATTTTCA[C/T]GTACTTTTTCTCTGT	23077
rs538376099	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77095272	AGCTAATAAAGTGTA[A/G]GTCAAATACCGAACT	23077
rs538376934	snp	A/T	0.166506	0.235645	intron-variant	MYCBP2	GRCh38.p7	13:77267414	AAAATAAAATAAAAT[A/T]AAATTAAATTAAATA	23077
rs538382321	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77141703	TTGAACCTGTGAGGT[A/G]GAGGTTGCAGTGGGC	23077
rs538419842	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77237559	ATTAGAAGATGACAA[C/T]GAAATAAAAACAATA	23077
rs538429465	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77304867	AAATAAGAAAGGAGA[C/T]ATCACTACAGATGCT	23077
rs538444181	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77289153	ATACCTCAAGTACCA[A/G]AAACACTTGGTCCCA	23077
rs538456040	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77151741	AACAAAACGGGACTA[A/T]CTTTGATCTACTAAC	23077
rs538463190	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77260006	ACACTGTGCTGGGCA[C/G]TGGGGATAGAATAGT	23077
rs538514352	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77165468	TTTTATCCAATGGAC[C/T]TTCTCTTTTATCACA	23077
rs538517386	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77144656	TAATTTGTTTGCATA[C/T]CTCCTGGCAATCCTA	23077
rs538529715	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77244719	AAAGTATCATCAGAG[C/T]GAACAGGCAACCTAC	23077
rs538537229	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77253338	TGTTCACAGCAACAT[C/T]ATTCATAATAACCAA	23077
rs538547203	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77282086	AAGAGGCAGCAGCAG[A/G]AAGAGAGGAGGAGAA	23077
rs538563908	in-del	-/AGACACATAC	0.00199481	0.0315187	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076317	AGAAAAATGAAGAAG[-/AGACACATAC]AGATTATTATGAACT	23077
rs538573758	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77252426	AAGAAAGACAGACAT[A/T]AATCAAATAACCAAA	23077
rs538575741	snp	C/G/T	6.81832e-05	0.00583848	intron-variant	MYCBP2	GRCh38.p7	13:77181668	TTTAGAGTTTTAGTG[C/G/T]CTCTGTATAAAAGAT	23077
rs538636846	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77289528	GAAAAAAAAAAAGTC[G/T]AAGTTAGGAATAGAA	23077
rs538636933	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77303754	TCTCCTTTTGCATAC[A/G]CATAAATGCATATAC	23077
rs538641233	snp	C/G	0.00478085	0.0486577	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77080156	CTTAGGTCTGAGGAG[C/G]AAATAGCTCATATTA	23077
rs538649038	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77311581	TTTTTTTTTTTTTGT[A/T]TTTTTTTTAAAGAAC	23077
rs538654433	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77166160	TCAGATCAGGCTGTG[C/T]CCCTTGCCCAGGGTA	23077
rs538657695	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77131773	TTTTAAAGGCAGAAA[A/T]GTTCTGTCAAGAAAA	23077
rs538662782	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77049118	CCCTTCCTCCAAGCT[C/T]AAGTCATCTAGAGTC	23077
rs538663709	snp	C/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77202846	ACAAAATTCAACAAC[C/G]CTTCATGCTAAAAAC	23077
rs538666759	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77064112	CTGAAGAATGCAATC[C/T]CATTTCCTCAAAGAT	23077
rs538703473	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77119977	AATAACAAATTTTCT[C/T]GGCAATGTTTGTGTC	23077
rs538703639	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77077987	TTCTTGACACTATTC[C/T]CTTCATAAAATAAAA	23077
rs538712219	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77260851	CTCAGTGAGTAATAT[C/T]AGTTTTCTACCAAAC	23077
rs538715370	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77047359	AGCAATACCTAACTC[A/T]TGGGGTGCTGTGAAG	23077
rs538751174	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77312987	CAAGTGTGTATAATA[C/T]AATCACCAAGACAGA	23077
rs538763056	snp	A/G	0.0123036	0.0774623	intron-variant	MYCBP2	GRCh38.p7	13:77296399	CCCTGTTTCAAAAAA[A/G]AAAAAAAAAAGGCAA	23077
rs538784576	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77313746	TCCAAAATACCAAGA[A/G]CTTTTTTCCCCATCT	23077
rs538786873	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77268578	TGGGATTAAGAGTTC[A/G]AGACAAGCCTGGCCG	23077
rs538789305	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77201992	AAAGGAACTAGAAAA[A/G]CAAGAGCAAACACAT	23077
rs538791365	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77159295	TAAAGTATATAATAC[A/C]TTGCCTAACAAATAG	23077
rs538799290	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77298366	TCATCGTATATTTAT[G/T]TTTCATTGTACAGCC	23077
rs538803565	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77168320	TCTATATGTAAATAC[C/T]ATAAAAGAAAATACA	23077
rs538813740	snp	A/G/T	0.00159649	0.0282165	intron-variant	MYCBP2	GRCh38.p7	13:77145420	TTTAATTTAAGGAAT[A/G/T]CCCCAGGATTTGGGT	23077
rs538841691	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77165649	AACTCCCCTGCTTAA[C/T]AAAGTACTTCAGTTA	23077
rs538851689	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77288530	ATGGACCCAACTTCT[A/G]GTCCCCTTTTCTATA	23077
rs538860665	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77306263	AGATTCATTCTGTGT[A/G]ATTAATGTAATGATA	23077
rs538880971	snp	G/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77152824	TAATCCCAGCACTTT[G/T]GGAGTCTGAGGCGGG	23077
rs538898238	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77063474	TGAGACAGGAGAATC[A/G]CTTGTACCTGCAGGC	23077
rs538907710	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77072027	GATACAGTGGCTCAC[A/G]CCTGTAATCCCAGCA	23077
rs538919693	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77220033	ACTGGTTGAATCTGG[A/T]AATTAAGTATCAATC	23077
rs538930633	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77080706	TAGCACTTTGGGAGG[C/T]TGAGGTGGGCAGATC	23077
rs538938726	snp	C/G	0	0	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291108	CAAAAGCAAGCCACA[C/G]AACAGGAGAAATGTA	23077
rs538956131	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77190438	AATGAAAATGATTCA[C/T]TCTTTTACATAAAGA	23077
rs538960385	snp	A/T			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77077895	AACTTCACACTTGTG[A/T]TTCCTTATTTCACTA	23077
rs539011902	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77312714	AGAAACAGAAGACAA[C/T]AAAGTGGCAGACCTA	23077
rs539024397	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77319818	ATTGCCAGCCAGCCA[G/T]CCAATAATCCAGCTT	23077
rs539030131	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77145324	CCTTCTTTTTGCTTC[C/T]GTGACATTTTCCTGG	23077
rs539036352	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77055019	TTGGGGGGTCATAAA[C/T]ATATACATGGTAGGT	23077
rs539043365	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77271156	CACATACACATTCTA[C/T]ATCAAATAATTTCAA	23077
rs539064969	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77111198	TATGAATAATTTTCT[A/C]TTTTCAACTTGTCAG	23077
rs539065842	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77157367	TAGCTGGGACTACAG[A/G]AGTGTGCCACCATGC	23077
rs539071931	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77058556	AAGTTATTTCTAATC[G/T]TTGTTTGAATATAAA	23077
rs539083021	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77220927	CACTTCATGTAATCA[A/G]TCTTTCAGTTACCAC	23077
rs539089031	snp	A/C/T	0.000626173	0.0176844	missense	MYCBP2	GRCh38.p7	13:77096361	TATTTTTCTCTACAG[A/C/T]GATCACATACCAGAT	23077
rs539089126	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77252564	ACTTTCCTAAAGGAT[C/T]TAAGTTATGAGGTTA	23077
rs539091078	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77105915	GATCCCAAGTATTAA[A/G]TTCCCTGAGTCATAT	23077
rs539108461	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77323175	TGAGGCATAGAAGTT[A/G]TGTAATATACTCAAA	23077
rs539131812	snp	C/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77052082	CATATTGCTTGCTGA[C/T]TGTATGTAGGGTGGA	23077
rs539131865	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77162894	TTTCCTGACCTTGTG[A/G]TCCACCCACCTTGGC	23077
rs539146659	snp	C/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77155100	AATATTTGAAAGATA[C/T]TGCTAAAAGACTGAT	23077
rs539147220	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77206282	TAAGAAGAAACAGAA[C/G]ATGTATATAAAATTC	23077
rs539152100	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77104871	ATAAAGCCATCTTAA[A/T]CTAAGTTTTAAAAAG	23077
rs539158118	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77213840	TGACTCAAACCTTCA[A/G]CAGTGGAAGGAGACA	23077
rs539189567	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77185746	AGCAAGCTGACTTTC[C/T]CCCCTCATTTTAGAA	23077
rs539197195	snp	A/T	1.66007e-05	0.00288098	missense	MYCBP2	GRCh38.p7	13:77263727	TCTAGCCAGTTTAAG[A/T]TGCAATTCTTGCTGT	23077
rs539198773	in-del	-/AT	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77112802	CCTCCTGCATTATTA[-/AT]ATTTCTTTCAACTGA	23077
rs539216655	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77088717	AATACTTTTAATTGG[A/C]TAATGCCTTTTAATT	23077
rs539229517	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77097072	CTGTGTGTATGGGCA[C/T]GCCACTGTTTCTGCT	23077
rs539230578	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77214077	TACTAAATATGGATC[C/T]GAACTTTGAGGATCA	23077
rs539239449	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77092550	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC	23077
rs539254439	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77198004	GTCCACTACGTTGTT[C/G]ACTATTCCGAAAAGA	23077
rs539259215	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77309524	AAAATTCAGAGAGAA[A/G]AATCCCAAGAATGGA	23077
rs539259418	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77172483	TTTTTATCAGATCAC[C/T]CTGGCTGTGCTGTAG	23077
rs539279436	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77148157	ATAATTTTAAAATTT[C/G]ATACTAAAATAGCCA	23077
rs539299810	snp	C/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77099715	TGGAAACCACAGAAA[C/T]GGTGGATCCTCAGAA	23077
rs539303161	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77195166	AAATTATATGCTAAT[C/G]ACTTAGAAATCTTTC	23077
rs539305503	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77085104	ACTGGCTGTTTCATC[A/G]TAACTATAACTAGAA	23077
rs539312175	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77238239	CAGAGCGAGACTCCG[C/T]CTCAAAAAAAAAAAA	23077
rs539317378	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77186341	ATTTAAAAATAAATT[G/T]TTCAGTGTTCCTGCT	23077
rs539338630	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77138426	AGCTAACTTTATAAA[C/T]GGATTTTTAAGAAAT	23077
rs539369323	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77245442	AAAAAAGAATGAGTT[C/T]GTGTTCTTTGCAGGG	23077
rs539385122	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77094183	AGAGGACAATTTCCA[A/G]AATGGAACTGTTGGT	23077
rs539388408	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77293886	CTTGATTTTAGCTCA[A/G]TGAGATCCATTTTGG	23077
rs539390902	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77045662	AAAAGTAAAAAATGT[C/T]CACTATAAAAAATTC	23077
rs539391768	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77216034	TCTTGGAGAAATGGC[A/T]GATTCTAGGACAGTC	23077
rs539393811	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77153363	GTGCTCGCCATCCTG[C/T]AAGGGGTTTGAGTGC	23077
rs539407541	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77115480	GTTAACTTTTACTTC[G/T]ATAACATTCTACTTC	23077
rs539431329	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77178190	TATGAAACTATACTT[G/T]CCACTTAATTTATAA	23077
rs539445628	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77085965	GTAGACTGTCCTATT[C/T]TTCCTTGCAGTCTGT	23077
rs539448905	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77124319	AAGATACTCCATCAT[C/T]ATTGCAAATTTCAAA	23077
rs539466175	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77254482	ACTTTTAAAATATTC[A/C]TTTACGTTCGTTTTA	23077
rs539477721	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77223960	ACCACCAGTCTCTCT[A/C]CTACTATTTGCAATA	23077
rs539521886	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77069533	TCATGAGGTCAGGAG[A/T]TCGAGACCATTCTGG	23077
rs539544669	snp	A/G	0.00716266	0.059414	intron-variant	MYCBP2	GRCh38.p7	13:77108626	AAGTGACATCCTGAG[A/G]AAGAGACAACGCTTA	23077
rs539564196	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77271533	CATCTTGAATTCCCA[C/T]GTGTTGTGGAAGGGA	23077
rs539566368	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77059015	AAAAAAAGTTCCCCA[A/G]TGTATAATTTCCCAG	23077
rs539593054	in-del	-/ACAC			intron-variant	MYCBP2	GRCh38.p7	13:77166977	ACAAAACACACACAT[-/ACAC]ACACACACACACACA	23077
rs539605367	snp	A/G	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77218978	GTAAGGAACAGAATT[A/G]ATGAAACTTGGCAGA	23077
rs539605702	snp	A/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77210894	CATAAATGAGAAAAC[A/T]GAGGCACACAGTCAA	23077
rs539612648	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77201182	ATATAGGCTCAAAAT[A/G]AAAGGATGGAGGAAG	23077
rs539637135	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77245548	ACTCATAAGTGGGAG[C/T]TGAACAATGAGAACA	23077
rs539641142	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77281811	TCATAAAAGTTTAGT[C/T]ACATCACATTTGGAT	23077
rs539644508	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77155762	TTCAATCAATACATA[C/T]TGAGGGGCTTCACTG	23077
rs539646062	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77210382	TATTTTTAGTAGAGA[C/T]AGGGTTTCACTGTGT	23077
rs539646765	snp	A/G	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77317516	GCCTCACCCTTGCAG[A/G]GCATCATGCCCAAGC	23077
rs539661516	snp	A/G	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77171476	AATATGACTACTGAG[A/G]AAGAAAAAATATTAC	23077
rs539676475	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77274834	AATTCTTTCACTCCT[G/T]TGTTAATTTCTTCCT	23077
rs539677483	snp	C/G	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77307540	CTGAGGTGGGAAGAT[C/G]GCTTTGGTCCAGGAG	23077
rs539689152	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77108893	TATTTTTAGTAGAGA[C/T]GGGGTTTCACTGTGT	23077
rs539695424	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77226732	ACAAAATCTACCTAC[A/G]TTATTACTTTCCTTT	23077
rs539729362	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77054380	TAAGTAGAAGAGTGA[A/T]CCAGTTAGATTTTAG	23077
rs539735913	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77249752	GAATAAATTTCAATT[A/C]CAACATTGTTAAAAA	23077
rs539783754	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77235074	TTTCTTTAAATATAG[C/T]TGAGTCACTAATTTA	23077
rs539792273	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77061999	TAATGTGCTTTGCAG[A/G]TTCAATGATTAATAC	23077
rs539806026	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77193742	TAGCAGCATGATGTC[A/G]GAGTACATGGGTAAT	23077
rs539810959	snp	C/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77287073	TTTGTGTTTTTAGTA[C/G]AGACGGGGTTTCACC	23077
rs539814305	snp	C/G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77134717	AAATTATTTTGGAAA[C/G/T]GATACAGTCATAATA	23077
rs539826177	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77173575	CTACGTAGGCACCAT[C/T]CCTAGACTCTTCATG	23077
rs539845883	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77155203	TGTTCTTATTTTTTA[C/T]TTAGGTAAGATGCTA	23077
rs539852912	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77147401	AATGGGCTGTAGGTA[C/T]ATGAAACTTGGCACA	23077
rs539858730	in-del	-/AAC			intron-variant	MYCBP2	GRCh38.p7	13:77221689	AACCACCAGCTAAAT[-/AAC]AACAACAATAGCCAC	23077
rs539892072	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77170871	TGAGCCACCATGTCC[A/G]GCCATAACCATGTTT	23077
rs539896863	snp	C/G	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77199949	GATGGGGAAAAAACA[C/G]AGCAGAAAAACTGGA	23077
rs539905828	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77280239	GTCTTTGGAGAAGTT[A/G]TCTAAAATGCTAACA	23077
rs539928408	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77125870	GCATGACACACTACA[C/T]CTTCAAGCTTATCAG	23077
rs539942885	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77279752	TATTGTGCAAACTCA[C/G]TTTAGGAAATATGAA	23077
rs539985293	snp	A/G	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77251689	AAGCCTCCCAACCAT[A/G]CTCCAAGCCAAGAGT	23077
rs539988329	snp	A/T	0.00119737	0.0244387	utr-variant-3-prime	MYCBP2	GRCh38.p7	13:77044909	ACACAATGTTTTTTT[A/T]TTTTTTAAATAACAG	23077
rs540011921	in-del	-/AATG			intron-variant	MYCBP2	GRCh38.p7	13:77102097	TTACTAAACATGTTA[-/AATG]AATGGTAAGCATTCA	23077
rs540013722	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77318308	TCATCGGTAATTTTT[C/T]CATGCACTCATAGGC	23077
rs540020184	snp	A/G	0.00597247	0.0543191	intron-variant	MYCBP2	GRCh38.p7	13:77221214	GTATTTCATGAAGAC[A/G]ATAAATTCAAGCAAT	23077
rs540022546	snp	C/T	0.000184457	0.0096018	intron-variant	MYCBP2	GRCh38.p7	13:77224557	AAACACACAGCTTTA[C/T]TTTTTCATTATATGC	23077
rs540050432	snp	A/G	7.16936e-05	0.00598679	intron-variant	MYCBP2	GRCh38.p7	13:77278749	CACTGAATGAGCCTT[A/G]GCTCTTACCTAGGAC	23077
rs540053624	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77294345	TCATCTTTGTATCCC[A/C]AACATCCAGCATAAT	23077
rs540054109	in-del	-/AGGAGA	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77246561	AGGAGGAGGAGCAGG[-/AGGAGA]AGGAGAAGGAGGAAA	23077
rs540058616	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77233988	ATCATTTCTTCTAAA[A/G]TGCCACTATGTACAT	23077
rs540070137	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77117428	AATGAATAATATCAT[C/T]TGCTAGCTACATACT	23077
rs540087598	snp	A/G	0.0260105	0.111035	intron-variant	MYCBP2	GRCh38.p7	13:77285907	AGGAAAGCAAAGGAA[A/G]GCAAAGGAAGGAAGG	23077
rs540097241	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77324831	AAAATTATTGCATAA[A/G]TCTGGAAACCATACA	23077
rs540103641	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77069279	CTGCTAGAAAGATAA[A/G]GCAAAAATAAATTCA	23077
rs540119801	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77157584	AACTCTGTTTCTACA[A/G]AAAATACAAAAAAGA	23077
rs540127062	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77287919	TATAACAGACTCCAA[C/G]CCACTGATCTCCCTT	23077
rs540127741	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77097198	GCCATCATAATATTA[A/G]AATTTATCTGTTTTT	23077
rs540145844	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77317204	TGATCCACTCATCTC[A/G]GCCTCCCAAAGTGCT	23077
rs540145950	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77178289	GCTAAAAATTTCATC[A/G]AAATTCTATAGATCA	23077
rs540149002	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77211850	TCTTTGAGCAGAAAG[A/G]AAACAAAAAGCTACA	23077
rs540154824	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77129007	TTCTTTTTGGCAGGA[A/G]TGAGAAAACTCAATT	23077
rs540165108	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77266244	AGAATTTTTCTTCTA[C/T]GTCATTATCCTAAAA	23077
rs540167690	snp	A/G/T	3.34645e-05	0.0040904	intron-variant	MYCBP2	GRCh38.p7	13:77068541	TAACAAAAGCAATGG[A/G/T]AAGGCTGTAGTGTGA	23077
rs540182622	snp	C/T	0.00155807	0.0278677	missense	MYCBP2	GRCh38.p7	13:77164510	CAAACCCCACCAAGA[C/T]TGGCTAATTCTTTTT	23077
rs540187163	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77200487	GATATTATCCAGGAG[A/C]ACTTCCCCAATCTAG	23077
rs540188462	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076537	TGCAAAAACCCAAGG[C/T]ATAGAGCAAATTTGC	23077
rs540198807	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77091599	CTGGCCTCAACTCAC[G/T]AGGATGCCCACTCAA	23077
rs540211710	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77099901	CAGTGTCTCTCCTTC[A/G]TTCTATTTTATGCTT	23077
rs540229952	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77308802	GAACTAGGGCCTGAA[C/T]CAGTGGAGAACTCTG	23077
rs540235123	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77218425	TCTTAGAATCACAGT[C/T]AATGAGTCAAAACAC	23077
rs540247649	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77309876	CTCAGTACTTTGGGA[A/G]GTCGAGGCGGGCAAA	23077
rs540253794	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77247802	AAAGGAGCCAAGATG[G/T]TTCAATAGAGAAAGG	23077
rs540268743	snp	C/T	0.00220507	0.0331311	intron-variant	MYCBP2	GRCh38.p7	13:77099226	CACCAAAAACTATTT[C/T]CATGGACGCAAAACA	23077
rs540274971	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77084298	ATGTTTGTTCTTCCA[C/T]CTTGCTACCAATGTA	23077
rs540286651	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77234027	ACATATATAAATACA[C/T]ACCCACACAGATTAT	23077
rs540322582	in-del	-/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77307307	GTTTACCCTTTATGC[-/T]TTTTTTCTGTGGTTT	23077
rs540325654	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77240652	AAAACATACAAGCAG[A/G]CATCACTTTGCATAG	23077
rs540343937	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77092672	CTCAGGTGATCCACC[C/T]GCCTTGGCCTCCCAA	23077
rs540346294	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77194546	TGCATCTGAAAAAGG[G/T]GAGAGAACTCCAACA	23077
rs540347343	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77053738	GCATGTATTTATCTG[A/C]CTTTCTGGCTATCAT	23077
rs540353969	snp	A/C			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77083708	TTGAATTTCATTTCT[A/C]ATTACAACCCTCAGA	23077
rs540360279	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77048650	AGCCCTCAATTTTCC[A/G]TTTGATAACATAGGG	23077
rs540361443	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77248613	CCAAAATAACAGATC[A/G]TAAGTGTTAAGAAGG	23077
rs540370812	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77109920	TTACAGTTTCTTATG[C/T]CTGTCTTTACTTTAA	23077
rs540386865	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77201831	GCAGAAATAAAGATG[C/T]TCTTTGAAACCAACG	23077
rs540390760	snp	A/C			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77080117	ACTTTCCAGTAAGAT[A/C]AAGTAGTTACACCAG	23077
rs540400536	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77164001	ATCTTCTCTTTCTTA[A/T]CTACTTGCTGTAGAA	23077
rs540404718	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77094345	CTGAGGTCCAATATA[C/T]GAAAACAGAATACTA	23077
rs540415998	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075952	AACACAGGGTGAGAC[A/G]AGGGAAATCCTTGAA	23077
rs540420650	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77230522	CAAATTTTGGAATAT[C/T]TGCATATACATTATG	23077
rs540429671	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77112669	GTCTCAAACTCCTGG[A/C]CTCAAGCCATCCTTC	23077
rs540442768	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77133205	ACCAGCTCCACTACT[G/T]TCTACTTGTGATCCT	23077
rs540457473	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77161404	CAAACAATAATAAAA[A/G]CAACAAATGATGGCT	23077
rs540463725	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77303327	GACAGAGCGAGACTC[C/T]GTCTCAAAACAAACA	23077
rs540464488	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77101969	ATCTCCTAATTTATT[C/T]AATGACTGTACTTTT	23077
rs540473487	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77170585	GAGGTAACTTTTTTT[C/T]TTTTTTTTTGAGATG	23077
rs540502028	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77225221	CCACAGGAAGACAGA[C/T]TAGAAGTTAGATCTC	23077
rs540503194	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77272097	ATTGGAGACAGATAA[A/G]CCCTCGAGTCCTGTC	23077
rs540521825	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77235779	AAAAGGAGGCACACA[A/T]ACTAGAGGAGAAGCT	23077
rs540521860	snp	C/T	6.59011e-05	0.00573988	missense	MYCBP2	GRCh38.p7	13:77243094	TGCCTTCTGATTACA[C/T]GTTGCCGTTTTTCTT	23077
rs540522777	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087061	TTGTTAGTTCTTGCT[C/T]ATGGTGTCTTGTTTG	23077
rs540528834	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77279374	CTGGTACTTTTCCTT[C/T]AATTATCTTACTATT	23077
rs540593544	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77213562	AAAAATAAATTAGTT[A/G]TCTTTTTCATTGACT	23077
rs540593915	snp	A/C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77196935	GTCAAAAACTGAGTT[A/C/T]TTGGCACTCCAACAT	23077
rs540595051	snp	A/C	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77051458	TGGCTGGTCAAACTG[A/C]AAATTAATGAAATTA	23077
rs540610233	in-del	-/A	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77146340	ATATAGGAGAAAAAG[-/A]AAAAAAATTACCTAC	23077
rs540613184	snp	C/G	0.00636936	0.0560724	intron-variant	MYCBP2	GRCh38.p7	13:77241045	ACTAAGTGCCTAGAA[C/G]CTCAATCTATCTTTG	23077
rs540617985	snp	A/C	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77251888	TTCCCTCTGCTCTCC[A/C]AACACCCTGTGTCCT	23077
rs540624244	snp	G/T	1.65151e-05	0.00287355	intron-variant	MYCBP2	GRCh38.p7	13:77064757	GCAGAACAGAGTATT[G/T]TAATAAGTGACCAGA	23077
rs540642530	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77069106	CTATGCTTACAGTTT[A/G]GCACGTCAAAAACCA	23077
rs540643970	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77045989	ACACTGGTAAAATGG[A/G]AAGGCCAATGATTCC	23077
rs540650567	snp	C/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77320777	ATACAATATTCTTGC[C/T]AAAAAATTTTCTAAT	23077
rs540655847	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77248816	CTCCTTGTACACTCA[A/T]CTTCACAGCGCATTA	23077
rs540662303	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77178611	CTTTGGGTTGAAATC[A/G]CTCTTTTTATTTACA	23077
rs540662920	snp	A/C/G	4.98611e-05	0.00499284	missense	MYCBP2	GRCh38.p7	13:77166361	ATAGTAGGCCACCCA[A/C/G]AGGATCCTGAAAATT	23077
rs540678926	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77258006	TGTAACTTTGTAACG[A/T]AGCTTCAGTGAATCC	23077
rs540692423	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77209420	CATTTAAAAATAAAA[C/G]ATGTAAGAACTACAA	23077
rs540693579	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77232762	CTGAATTTAGTAATA[C/T]TGTTTATCCTAAAGC	23077
rs540701816	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77282428	AAAAAAAAAAAAAAA[C/G]AAAGAAAGTATGAGT	23077
rs540702171	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77295644	TTGTTTCTTTAACTC[A/G]AAGTGAAGCTATTCA	23077
rs540706891	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77214097	TTTGAGGATCAGAGC[A/C]CCAACTAAAGGCAAA	23077
rs540740727	snp	C/T			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77294066	ATGGATGAGGAGAAA[C/T]AGAGGGGTTGATGAT	23077
rs540756889	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77156303	AAAACTTGTATCAAA[A/C]AAAATGCTAAAACAT	23077
rs540769849	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77182917	GTAAATATCTTTTTA[A/T]CAGATTTAGGAGTTT	23077
rs540776838	snp	C/G	0.000310434	0.0124547	intron-variant	MYCBP2	GRCh38.p7	13:77099192	AATAAAATTTCTACA[C/G]ATCATTACACAACAT	23077
rs540781506	in-del	-/T	0.00119737	0.0244387	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77077777	ATCAGAAAAGGGTTC[-/T]TTTTTTGTGCATCCT	23077
rs540805403	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77097170	TGAAAGTGAAATAGC[A/G]CTAAATGACCTGGCC	23077
rs540807086	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77056017	CTTTATATTTCCTGC[A/G]TCTGAAATATATCTC	23077
rs540808773	snp	A/G			intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326420	GTGCACGCGCGGCAT[A/G]GGGCGCAAGGAAGGG	23077
rs540867111	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77106428	TTGTAAACAGGCTAT[C/T]CAGAAGGACAATATA	23077
rs540868115	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77202289	TAAACTAGAAAATCT[A/G]GAAGAAATGGATAAG	23077
rs540875900	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77077438	GCTGGATCACTTTTA[C/T]CACTGTGCTGGACTT	23077
rs540877694	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77323542	CCTAAAATAGCCCCA[C/G]TACAAATTGCCCTAT	23077
rs540888655	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77160313	CTGTATGATCGTGGG[C/T]GAACTGCCTAAATGC	23077
rs540888924	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77254037	ATGTTCACTGTGTGG[C/T]ATATTACACATTAGT	23077
rs540913177	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77207324	TCAACCATATGAATA[A/C]ACAGTAAAAACCAAT	23077
rs540914570	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77320597	ACAATGTGCTCAAAT[A/T]TTTACCCTGTGATTA	23077
rs540915365	snp	A/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77302751	CAGTGTCCCAAAAAA[A/T]GTTGGAGTGGCTATT	23077
rs540919368	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081243	TTCAGAAATGGAATT[A/C]CACAGTGCTCCCAAT	23077
rs540951124	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77187698	AGAAACAAGCAAGCA[C/T]GTTGTAGAGCATCCT	23077
rs540958975	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77245809	AAACATTCACACATT[C/G]GAAAGGAAAAAATAA	23077
rs540970849	in-del	-/TTATTA	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77258737	TAAAACAGTAGTTAT[-/TTATTA]TTATTATTAACAGTA	23077
rs540981009	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77089837	TGGTTGTAACATTTG[A/G]CTTAGATACCTAACA	23077
rs540987577	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77130853	TGAAAGGCAATTGTT[A/G]AAAGTAATGCAGGTA	23077
rs541006684	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77258779	GACATGCTTTGAGAC[C/T]TTACATGATGTGCTA	23077
rs541007627	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77145987	GTATTACAGTTGAAT[A/G]TAAACACATTCTTTC	23077
rs541031308	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77065131	AGGAACCTAAAATAT[A/G]AACAGGTTCAAACTG	23077
rs541044859	snp	C/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77239014	AATCCCAGCTACTCG[C/G]GAGGCCGAGGCAGGA	23077
rs541051333	snp	A/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77049654	CTGCAATTTGCTTTT[A/T]TTTTTTGAAACAGCT	23077
rs541064068	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77320293	ACATGTGCCTGAAAG[C/T]GGGATCTGAAAGCCT	23077
rs541094221	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77152636	AACTGATGAGACGCG[C/T]GGCTTAACCTCAGAT	23077
rs541096087	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77160088	TTTTTTTTTTTGAGA[C/T]GGCGTTTCACTCTTG	23077
rs541096663	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77056783	TGTTTAACAGAATGT[A/C]ATCAGTTTTAAATGG	23077
rs541101392	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291508	GGGTGCAGTGACTCA[C/T]GCCTGTAATCCCAGC	23077
rs541101709	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77277703	ACAAACTTTTGGGCC[C/T]CACCCCAAGTCTATG	23077
rs541101744	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77269845	AGACAGTGTTCTTTA[C/T]GCTACACTATTCAGT	23077
rs541103126	snp	C/G	0.00597247	0.0543191	intron-variant	MYCBP2	GRCh38.p7	13:77206534	GATTTAACTTATTTT[C/G]TACATTATTATTATT	23077
rs541119830	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77168321	CTATATGTAAATACT[A/G]TAAAAGAAAATACAC	23077
rs541131484	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77113143	CTCATGTTATCCTTA[C/T]AGTTGGAATGCTCCA	23077
rs541138735	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77277181	GACATCCAAGTCTTC[A/G]CGGGTATTTCAACAT	23077
rs541160842	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77222667	CAAGCCTTTCAACAC[A/G]CACATCTCTCAGAAA	23077
rs541217487	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77161216	GATTACTAGCTAGCT[A/G]AAGTCAGACTAATGA	23077
rs541218760	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77298655	TGGTATCGACATGAG[C/T]GCATTTAAAGCATCT	23077
rs541219120	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77306881	GATGGTGGGATTTTC[A/G]GAAAGATTGCAACAA	23077
rs541228414	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77107201	GATATTTTTGACAGC[A/G]ATAGGCTCCTACAAG	23077
rs541231290	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77306515	AATAAAGCTACCTTG[C/G]CAATGGGCAGAGCAG	23077
rs541231440	snp	A/C	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77153019	GCAGTGAGCTGAAAT[A/C]GTGCCACTGTACTCC	23077
rs541234735	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77050188	GCTGAAGGGTTGATA[C/T]GCTGGTAATTTTGAG	23077
rs541246321	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77314974	ATTATCAGAGATCCC[A/G]TAGACCTTAAAGGAT	23077
rs541252084	in-del	-/A	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77159988	TGCCAATGGCTTTTT[-/A]AAACTCAGACGTTTC	23077
rs541263658	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77123633	ATATTAGGTTAACTT[A/G]GTCAAGGTCACATGA	23077
rs541268285	snp	A/C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77058030	TTTTTGTAGTAGAGA[A/C/T]GGGGTCTCACTGTGT	23077
rs541271152	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77091033	CTCCTTTTTCTGTCA[C/T]CTGAATTCAAATTGG	23077
rs541277426	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77157824	AGCAAGTTAAACATA[C/T]ATAAACCAGACTTTT	23077
rs541296347	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77146509	AATACTATACAGAAA[A/G]GAAAAGCTTCCACCT	23077
rs541301090	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77114055	GCTGAGATTATAATC[C/T]GGGGTAGAAATGACT	23077
rs541318116	in-del	-/G	0.00795532	0.062565	intron-variant	MYCBP2	GRCh38.p7	13:77234985	AAATCAAGAAGGCAC[-/G]GGGGGCAATCATGTC	23077
rs541349718	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77254665	ATATATTGTTGTTAA[C/T]GACATTCACCCTACT	23077
rs541353452	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77161760	CCAAAGGGAGCAATG[A/G]TAAGTTATTTATCTC	23077
rs541381780	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77207477	GCAAGCTATTGTTTA[A/G]TAACTATAGAGTCTC	23077
rs541392952	in-del	-/AA/TA			intron-variant	MYCBP2	GRCh38.p7	13:77234843	TTAAGGTAATAATAT[-/AA/TA]TGTTATATTACCATT	23077
rs541405515	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77263293	AATAACATTTACAAC[A/G]TAAGTTTTCAAATTT	23077
rs541406518	snp	C/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77314384	TCCAAACTCACCAAA[C/T]TGTAGGTGAACAGAC	23077
rs541429238	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77056838	ATAACAGAGAGATTA[C/T]ATTCTCAGGTTCCAC	23077
rs541433969	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77106508	TATCACTGTCACCAA[C/T]ACTCAGAGCAGGTGA	23077
rs541437741	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77139497	CTCCAGGGAAAAAAA[A/G]AGCAGCAAAGAGTGC	23077
rs541438267	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77194114	ATTTTTAATATTAAG[C/T]ATGCAAGAGTTACAA	23077
rs541458002	in-del	-/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77250902	AAAACTTATGGTCTG[-/T]TTTTTAAATAATGGT	23077
rs541459273	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77138215	TCTCTGTCTATATAC[A/C]GTCTCCACTGTGCTA	23077
rs541469717	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77321620	TCATGACACCTGCAT[C/T]CTAGCTCTAACAGAA	23077
rs541509275	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77232875	AGCAATAATTATTTT[C/T]TCCACCTTCCCTTAA	23077
rs541520014	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77254819	CTATCTCCATGAAAT[C/G]AATTTTTTAGTTCCC	23077
rs541532113	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77307087	ATCTAGAAAACAGAT[C/T]AGAAAAAGAATCTGG	23077
rs541592811	snp	A/C	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77164120	TCAGTTGTCTACTTG[A/C]TATTTCCACTAGAAT	23077
rs541605248	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77169035	ATAAATGTGAAAAAC[C/T]TCAGTTAACATAATC	23077
rs541610219	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77215469	AGTGAGAAATAAATA[C/T]ATTGATATTGTTGAG	23077
rs541619190	in-del	-/C	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77217548	TAACCTTTCCTATGA[-/C]AGAATTAGCTCTATT	23077
rs541619608	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77223556	AAAGACAAGTAAGAG[C/G]GACTTCAAGATACAA	23077
rs541644634	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77067148	TTTAAGAAGGTCTTA[A/T]CAAATTGAAGATTAC	23077
rs541647911	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77199381	TCCTGCACCTGACTC[A/G]GAGGGTCCTACGCTC	23077
rs541667165	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77299354	GTTGTAACAATTCTT[A/G]TGAATCTGAACCCAT	23077
rs541669893	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77089892	TTCTCGAACAATCAC[C/T]GAATGATCTCCAGAT	23077
rs541676885	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77315711	ACCAGAGTGGCCAAC[A/G]TGGTGAAATCTCATC	23077
rs541681584	snp	A/C	0.000134837	0.00820976	intron-variant, nc-transcript-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77083022	TAGGATATGTGGATA[A/C]CAAAATTACCTCAGG	23077
rs541683049	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77246700	CCCTACAGACCAATA[C/T]CCCTTATGAATAATG	23077
rs541691775	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77238120	TGGTGGTGAACGCCT[A/G]CAGTCCCAGCTACTC	23077
rs541692998	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77206468	CATAAATCTTTGATA[A/G]TGTTAGTACAGGTCT	23077
rs541710093	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77231947	TCCTTAAATATTTAT[A/G]GCATTGTTAGAGCAC	23077
rs541728358	in-del	-/G	0.00320898	0.0399273	intron-variant	MYCBP2	GRCh38.p7	13:77248153	AATCAAAAAAAAAAA[-/G]AAGAAGAAGAAAAGA	23077
rs541729244	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77209372	TTCCACACTGCCAAT[G/T]TTTATTTTTGTTTTG	23077
rs541744946	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77082068	ACTCTTAGATGAGTA[C/T]TCTGTAGCTAATATC	23077
rs541749606	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77058595	CTTAACAAAGTTTTT[C/T]TTTTTTGATGCGATT	23077
rs541760818	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77183872	TTCACTTTTGATTAT[A/G]GTATTTCATGTTTTT	23077
rs541775323	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77123781	TAGAAGTCACCTAAG[C/T]TGTTCTCATATTTAA	23077
rs541787976	snp	A/C/T			intron-variant	MYCBP2	GRCh38.p7	13:77198055	AAAAAAAATATCCTC[A/C/T]TGATGAGCTTATTAG	23077
rs541808367	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77141113	CAAGAGAAATATTTT[A/T]AAAATGGCCCTGAGA	23077
rs541809991	snp	C/T			intron-variant, downstream-variant-500B	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087890	GGCACAAATGATCCT[C/T]CCACCTCAGCCTCCC	23077
rs541811184	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77113737	AAAATACCTGGGTCA[A/C]AGCTTTTAGGTCACT	23077
rs541824279	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77232961	CTTTATGAAAGCTAA[C/T]GACAACAAAAAAACA	23077
rs541831609	snp	A/C	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77261498	ACATAAAAACAAACT[A/C]TTTTTTACACTATTC	23077
rs541839012	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77122886	CCTTAGGCAATACTC[C/T]TCAGCATGCAATATT	23077
rs541866282	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77152508	AGTTTATCCTTGTAT[C/T]CCGCCTAAATGTTGC	23077
rs541867686	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77179945	GGGTAAACTGGTGAG[A/C]GAGAAGTAACAAATC	23077
rs541885801	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77263362	ACATTCACCAATATC[C/T]ATCCATAATTCTCAT	23077
rs541888594	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77050770	GACTTCATTCTCACT[C/T]CCCATGAGATCTGCT	23077
rs541891414	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77183405	TAATTTTTAAATGGA[C/T]ATGAGGCAATTCAGA	23077
rs541895900	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77134900	TAACGATGAATACAC[A/G]AATTCTAAAACATGA	23077
rs541912326	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77115030	CACAGTATAGTTGGC[C/T]TTAATTACTAAGAGA	23077
rs541913179	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77153723	ATGTGACTTTCTCTT[C/G]TCAATAAATAAGATT	23077
rs541930111	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77068288	TTTCTTTCTGGTCAG[C/G]GCTAAATGACATTAT	23077
rs541930506	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77190913	GAATATATACTGTTA[C/T]ATAACTTCAACTGAT	23077
rs541933579	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77160911	AAAGTAGTACATTTT[A/T]AAAGAGTGTTTTTAC	23077
rs541934273	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77215566	TGGGAATGGATTGGA[A/G]GTAGAAGTCACAGTG	23077
rs541958798	in-del	-/CAGGGGGTTATGAC	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77063347	TGGATCACCTGAGGT[-/CAGGGGGTTATGAC]CAGCCTGACTAACAT	23077
rs541962893	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77270831	TTGTGGAACTCAGAT[C/T]GTATTACATTAGATT	23077
rs541972701	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77153109	TGTATTCACGCATTC[A/G]TCGCGTTTCAAACCA	23077
rs541993328	snp	A/C	3.65845e-05	0.00427679	intron-variant	MYCBP2	GRCh38.p7	13:77262032	AGAATGCTCATTTTT[A/C]ATCCAAAGAGAATAA	23077
rs542001065	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291596	CACATGGAGAAACCC[C/T]GTCTCTACTAAAAAT	23077
rs542002785	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77299976	GAACAAATCAATTTT[G/T]CAAATTATTCAGTGA	23077
rs542003008	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77209413	TTTACTTCATTTAAA[A/G]ATAAAACATGTAAGA	23077
rs542044609	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77308949	GCGCATGTGAGTTGC[C/T]CTGCACACAGGCCAA	23077
rs542047099	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77115794	TTTCTAGTTAACCAG[G/T]ATCTTGAGTTATGAC	23077
rs542055800	snp	C/T	3.30535e-05	0.00406518	synonymous-codon	MYCBP2	GRCh38.p7	13:77098376	CTCACTGTGGAGGTT[C/T]TCCTGTACCACATGG	23077
rs542067374	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77154685	TAACAACTCACTACA[C/T]TGAGAAATTCATCAG	23077
rs542069034	snp	C/T			missense	MYCBP2	GRCh38.p7	13:77051875	TCATAATCATCTCCC[C/T]GTCCAGCCTCAGCAT	23077
rs542077965	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77257113	GGAGGATATTATGTT[A/G]AGTGAAAGAAGCCAG	23077
rs542086811	snp	C/T	0.000399281	0.0141238	missense	MYCBP2	GRCh38.p7	13:77140118	GAAGGGAAGGGTGGC[C/T]ACGGATGCGAAGCCC	23077
rs542109291	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77193589	TAATTCTTAGGATTA[C/T]GTAGAGAGGACTGAT	23077
rs542109775	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77175344	TATTTTTAAGAAAAA[C/T]TCAGAGATAGAAATA	23077
rs542130664	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77301213	TGAGGTCAGGAGTTC[A/G]AGACCAGCTTGGCCA	23077
rs542139625	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77047348	AAAATAGACACAGCA[A/C]TACCTAACTCATGGG	23077
rs542165961	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77296384	GGTGACAAAACAAGA[C/T]CCTGTTTCAAAAAAG	23077
rs542176312	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77210406	ACTGTGTTAGCCAGG[A/T]TGGTCTCGATCTCCT	23077
rs542183251	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77147335	AATCTGTTTCTTAAT[A/T]AAAAAATAACAAAAT	23077
rs542189949	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77161990	TTTTACTAAAATATG[C/T]CAATATTTAGTTTAG	23077
rs542206974	snp	C/T			intron-variant, downstream-variant-500B	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77088086	ACTATGCTTGGCACC[C/T]TGAAAATCTGACCTT	23077
rs542219890	in-del	-/AGA	0.0150606	0.0854603	intron-variant	MYCBP2	GRCh38.p7	13:77122032	ATATTTTTCCCAAAT[-/AGA]AGGATAATAATAAAC	23077
rs542221406	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77176190	TACAGATAAGTCTCA[A/G]AGTGGTTAAATAATG	23077
rs542224083	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77236320	AGCTACACTCATGTG[C/T]AGACAATGGGTAATT	23077
rs542226550	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77131741	TATATAAAATAACAT[G/T]TCATTCTCAAATACT	23077
rs542230184	snp	C/T	1.90065e-05	0.00308268	missense, intron-variant	MYCBP2	GRCh38.p7	13:77126535	TCATCAGTATTAGTT[C/T]TAGATTCCTGAAAAT	23077
rs542255988	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77198882	AAAGGCACTGGTATT[A/G]CTAGGCCACCAGAAG	23077
rs542262064	in-del	-/A	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77116924	TTCTCCTTTCTCCTT[-/A]GTTCTTTTGTCTGCT	23077
rs542263145	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77069581	CGTCTCTACTAAAAA[A/T]ACAAAAATATTATGC	23077
rs542286015	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77224240	ATCAGCTTTTCTCCT[A/G]AAACTACAAAATCCT	23077
rs542292697	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77188136	AATAGTAGGTATATA[C/T]GGTGATCATGAGAAT	23077
rs542305152	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77315002	GATAATGAAAGAATG[C/T]TATGGATAACTTCAT	23077
rs542313394	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77212399	ATTTTTTAAAAAAAA[A/G]TTTGAAATATTTTCC	23077
rs542317590	snp	A/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77169348	TTGCAGTGAGCGGAG[A/T]TCGCGCCACAGCACT	23077
rs542337689	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228455	AAGGCTGCAGTGAGC[C/T]GTGATCATGCCATTG	23077
rs542343197	snp	C/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77067325	TTTTGTATATGGTGA[C/G]AGGTAGGTATCTAGA	23077
rs542367951	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77281538	AGAAAATAGTCTTTT[A/G]TAAATTTACTGAATT	23077
rs542379007	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77169137	CAACAGGCCGGGCGC[A/G]GTGGCTCACGCCTGT	23077
rs542380745	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77177420	GATTATGGCTCACTG[A/C]AGCCTCAACCTCCCG	23077
rs542381784	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77108669	ACAGCTAAAACCTAA[A/G]CCAAAAACAGAAGTG	23077
rs542384004	in-del	-/GGAAA			intron-variant	MYCBP2	GRCh38.p7	13:77285858	AAAGGAGAAAGGAAG[-/GGAAA]GGAAAGGAAAGGAAA	23077
rs542395906	snp	A/T	0.00835141	0.0640778	intron-variant	MYCBP2	GRCh38.p7	13:77267439	TAAATAAAATTAAAT[A/T]AAATTAAATAAGGAG	23077
rs542397071	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77317330	ACAGGATTCTCATAG[C/T]GCCCTCTGTTGGAAA	23077
rs542416823	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77092097	AAAAAAAAAAAAAAC[C/G]TCATTTGGATATATA	23077
rs542420726	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77162344	GACTTTAGTAAACAA[C/T]AGGGACTCACAGAAA	23077
rs542427496	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77072933	TGAGTCTCTTTTAGA[C/T]AGTTCTTTCATCTTG	23077
rs542438844	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77119476	TTTTTTGAAATAATA[A/C]ATAAATGCTGTAGAT	23077
rs542447544	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77216384	CAGGAAAGAATGATC[A/G]ATGGATGCTAAATCT	23077
rs542450368	snp	A/T	0.00676609	0.0577691	intron-variant	MYCBP2	GRCh38.p7	13:77059075	ATTTTTTTTTTTTTT[A/T]AAAAGGTACCTTTGA	23077
rs542466103	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77106529	GAGCAGGTGAGATAA[C/T]ACAGATAAAAAAAAT	23077
rs542475518	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77260351	GCCACCAACATAAAT[A/T]TTCTAGATATGTCTT	23077
rs542481132	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77209595	TATCCCACTGTGACC[A/C]TTCTAACTTTGGTTC	23077
rs542491340	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77315984	TCAAATTGATAGAGG[C/T]CATTGAAACACCTAC	23077
rs542501004	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77220248	ATAAAGTTAAAAAAA[A/G]GGTGAAAAAAGAGTA	23077
rs542511652	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77309704	AGAGTTACTGCAACT[A/G]TCTCTTTAAAGGTAG	23077
rs542518776	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77100041	CCAGTTAGTTGTTAG[A/G]AGAAAAGCAATCTGA	23077
rs542527787	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77312873	CTAAGAGGAGAAACT[A/T]TAAATATAAAAACAT	23077
rs542535967	snp	A/G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77313876	CCTCACCGAACAAGA[A/G/T]ATATAGATGGCAAAT	23077
rs542549593	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77225833	ATAAACGGGTCATTA[A/G]GTTATAGAAATAACA	23077
rs542557890	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77155264	TGAAAGAATGCATGA[A/G]GTAGTTGAAATAGTT	23077
rs542558300	snp	G/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77200589	CCAAGGCACATAATT[G/T]TCAGATTTACCAAAG	23077
rs542563167	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77259415	CCATCAATCACTAAT[A/G]TATCACCCATGCTCA	23077
rs542569191	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77104185	CAGGTAGTAAGGAGA[C/T]AGTTGTCTTAGTATT	23077
rs542588067	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77052179	CCTTCCTTCCCTTCT[C/T]TTCTCTTCTCCTCTT	23077
rs542606646	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77297812	ACAAAATCTGGTCAA[C/T]TATATCTCATAAACA	23077
rs542637033	snp	A/G	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77069869	CGAGACTCCCTCTCG[A/G]AAAAAAAAAAAGTTA	23077
rs542640102	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77196716	GAAGAACATGAGGAT[A/G]GCAGGTTTAGGCAGA	23077
rs542645032	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77180445	GTCAATTTCTACAAA[A/T]CTTTCTGGTTATATG	23077
rs542646637	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77198051	TAGAAAAAAAAATAT[A/C]CTCCTGATGAGCTTA	23077
rs542658282	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77167689	TCTTTATATTTTGGA[G/T]ACATTGTATCAATAA	23077
rs542658504	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77164879	ACTCAGAAAGGTATA[C/G]CCAACTGAGCAGGTT	23077
rs542663005	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77305322	AATGTATAAAGTGTA[A/G]CACTTCCATATAAGA	23077
rs542676195	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77182142	ATTAAGTCTGGTCAA[A/G]AAAAATCAGGCTCCT	23077
rs542678639	snp	C/T			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77227402	CCAAAATAAAATATA[C/T]TCAGTTCAAAGCCTC	23077
rs542685214	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77219353	GCACCACAATGCAGC[A/G]GATAAGGAGTCAGAG	23077
rs542712718	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77062843	AAGTCTTCCTGATGT[G/T]GTAGCAGGCATACAC	23077
rs542715872	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77273971	TCATCCTATCAAGTA[A/G]TAGACTACTTGTCAT	23077
rs542715978	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77080103	CTTTGTTACACTTGA[A/C]TTTCCAGTAAGATAA	23077
rs542731377	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77289650	CAGGCAAATTGGTCT[A/G]CTCTCAGCAACTCAT	23077
rs542736525	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77137962	AAAAAAAACTGTACA[A/G]AAGTGGTTGCTATAA	23077
rs542753419	in-del	-/AG			intron-variant	MYCBP2	GRCh38.p7	13:77255464	CGCTCAATTTTCACA[-/AG]AGTTTCAGAATAAGG	23077
rs542757104	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77189667	AAGTATTGCAGTAGT[C/T]TAGAAATAAATAAGG	23077
rs542764834	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77047851	CGGGCCAAGACAGCC[C/T]ACAGACTAAGCACAT	23077
rs542767765	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326954	CTTCTCCTCCTCCCC[C/G]CCGCGCCGCCCTCGC	23077
rs542771300	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77320324	AACCACAGCACCTGC[C/G]ACACCACCACTGGAC	23077
rs542772000	snp	C/T	0.000593257	0.0172127	intron-variant	MYCBP2	GRCh38.p7	13:77070611	AACTAATGAAGACAA[C/T]GAAATAGCTGTTAAC	23077
rs542779269	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77103355	GCACAGATTCAATGG[A/G]AAAAAAATTTAGCAG	23077
rs542783097	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77290358	CAGCAATTATGTTCT[C/T]GGACATTTACACCAG	23077
rs542788546	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77173472	CAACAATGAACTACA[C/T]AGCTATTTGCTGCCT	23077
rs542794970	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77145961	AGGTAGTATTATGTA[A/C]TATATTGGCAGTATT	23077
rs542798039	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77112232	TGGATAACTATTTAT[A/G]ATCCCACTTAGCCAA	23077
rs542811995	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77054816	ATCTTGCCCTGGGTG[C/G]TCTCAAACTCCAGAG	23077
rs542842572	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77110748	TCTCAGACTGGCCAA[C/T]GCTTAGGGAAAATAG	23077
rs542844153	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77290663	TTAAAATGGCAAAAT[C/T]ATAAATGCTGAACAG	23077
rs542847119	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77283359	ACTCCCTATCAATCC[G/T]TAAGGCACTAGAGAA	23077
rs542847362	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77063626	TTCTGAGGCTTAAAG[C/G]GTAAGCTTCAGTTTT	23077
rs542849109	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77072368	TGTGAATTGAATGAA[A/T]ATAAAAACAGAATAC	23077
rs542882792	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77056094	ATAAGACACGCTCTG[C/T]GTTTGGTGTGTGTGT	23077
rs542886407	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77212271	AACCTTATTTTTCAC[C/T]AATTGTTAGTTTGGG	23077
rs542902424	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77167264	CATGTGTGTGTATGT[A/G]TAACAGAAATCAGGA	23077
rs542924160	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77310615	AGTATCATATATATA[C/T]AATTGGATTCCCAGA	23077
rs542930814	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77221836	GAATTGGTTCCAGGA[A/T]CCCCTGCAGCTACCA	23077
rs542959496	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77276075	ATCCAACTCTCTGAT[A/G]CTAAGTTCCATAATA	23077
rs542960039	snp	A/G	1.67548e-05	0.00289432	synonymous-codon	MYCBP2	GRCh38.p7	13:77205552	TTCCTCTGTACTTGC[A/G]ACACCCATTTTTAAG	23077
rs542990488	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77137974	ACAAAAGTGGTTGCT[A/T]TAATTATCTCTTTAA	23077
rs542993734	snp	A/G	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77062859	GTAGCAGGCATACAC[A/G]ATCACTGTCCTATGT	23077
rs542997812	snp	A/G	1.81168e-05	0.00300966	intron-variant	MYCBP2	GRCh38.p7	13:77189092	GTTAGAAAGTCCAAT[A/G]TCATTTTTTCTTTTT	23077
rs543025905	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228597	ATCTATATAAAAAAT[A/T]AAACATTGTCAATAA	23077
rs543030324	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77244232	CACTACTTTAAAAAC[A/C]ATCCTTTAAAAGTCT	23077
rs543034092	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77287592	TTGGTTCATAGGTGA[C/T]TTTTTTTTTTCCTAA	23077
rs543034597	snp	A/C	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77197652	CTGGGTCTTTGAGGA[A/C]CTCCTACATTCAGTG	23077
rs543043902	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77262290	AATATTAACCATAGG[G/T]ATAGTACTCCAAGGA	23077
rs543048021	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77314527	ATCTGAAAAGGCCAC[A/C]TACTGTATGATTTCA	23077
rs543049520	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77071718	TGAATATTATTGATC[A/T]ACTTGAACTAACTGA	23077
rs543068700	in-del	-/T	0.29936	0.245079	intron-variant	MYCBP2	GRCh38.p7	13:77195025	TTTAAAAAATGTCCT[-/T]TTTTTTTTTTAAGAA	23077
rs543087162	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77158352	AGATCTGCATGCTGG[A/G]TAAAATGGTGTATCT	23077
rs543090387	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77304736	CCCCATGTATAAGTA[A/C]AATTATTTGTGAATT	23077
rs543090943	snp	A/G	3.34459e-05	0.00408924	intron-variant	MYCBP2	GRCh38.p7	13:77095627	AAAAAAATCAAACTA[A/G]TCTTTTCTGACTTAC	23077
rs543091714	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77049281	TTGCTTCTTTCAAAG[C/T]CTGCTACTTCTATTA	23077
rs543110782	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77320222	TCAGGGCAATGCGTG[A/G]AGTGGGACTCAGCTG	23077
rs543119533	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77268124	AGTCATACATTATTG[A/G]AAATTGATGTAACAT	23077
rs543120011	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77111394	GCATAAAAGTAGATG[C/T]CATTTGAGACTGGCT	23077
rs543128517	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77079359	GTTCTATCCCCCAAG[A/G]TACTTGCCAAACTAG	23077
rs543141385	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77237871	AAAAAGAGACTTTTA[C/T]GTGTCACTGGAATAT	23077
rs543149240	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77136961	CTTTCTTTTAACTTA[C/T]AAAACTCTCAAGTCA	23077
rs543156112	snp	C/T	0.000923894	0.0214731	synonymous-codon	MYCBP2	GRCh38.p7	13:77260525	GCAGGCTGTATATAC[C/T]ACAATCTTTCCTTCC	23077
rs543159499	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77275460	TGCCTAGAGCACTTA[C/T]AATCGAATTCACTCC	23077
rs543160851	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77318349	CCAAACAGTAGTGTT[-/A]TATTAAGTAGTTAGA	23077
rs543174239	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77328087	GACAAAATAATTTAT[A/G]AGTTCTGTCATCCCA	23077
rs543188925	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77109827	ACTTTTATAATTTCT[A/T]ACACCTGTTTTTACT	23077
rs543189210	snp	A/T	2.10826e-05	0.00324667	intron-variant	MYCBP2	GRCh38.p7	13:77260380	TTTGTCATACATAAC[A/T]AGTATTGAAACTTCT	23077
rs543197002	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77080810	AGCCAAGCATGGTGG[C/T]GTGTGCTTGTAATCC	23077
rs543197930	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77120758	CAGTCCATGATGCTG[G/T]TCTCTTCCATTAATG	23077
rs543204908	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77206480	ATAGTGTTAGTACAG[G/T]TCTCATGTATTGTTT	23077
rs543229649	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77173262	AACACTGTATTTTGT[A/C]TAAGATATAAAGTTT	23077
rs543235921	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77282636	CTTGTGCCTACATAG[G/T]GATAACTCCCAAATC	23077
rs543236427	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77186396	AAACAAGGGAAAAAT[A/G]AGAAGCACTTATAAA	23077
rs543237279	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77124101	TCAAGTTGTGCTCAA[C/T]GTGTACAGCATGGTG	23077
rs543263215	snp	A/C	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77253777	AGCCACCAAACTGAC[A/C]AAAATCAGTCTGTCA	23077
rs543264111	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77212795	TAGGGACCTGGTCAG[A/G]TAAGAGTTTAATTTA	23077
rs543299392	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77144959	CTCAACATTTTTATG[C/T]TGCAATCACCTTGTT	23077
rs543334444	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77073040	TCTGTTTAAAGCATA[G/T]AATTCAATGGTTTTT	23077
rs543342620	snp	C/T	1.64855e-05	0.00287097	missense	MYCBP2	GRCh38.p7	13:77166443	GTCCATATCCTGAAT[C/T]CTGAACAGTTCTGAC	23077
rs543384042	snp	C/T	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77319287	AACCCCTCTAGCTAG[C/T]AGAAGAAGGCCACTT	23077
rs543387678	in-del	-/AACT	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77179826	TCTTCCAGCAGTGAG[-/AACT]ATCTTTGCTTTTCAC	23077
rs543394341	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77274769	TACCATTCGCTTTTG[C/T]CCCAATAGCCAGGGA	23077
rs543400930	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77152545	GGCCAGCCCTGCCCC[C/G]CTACCCTATGCCCCT	23077
rs543403201	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	MYCBP2	GRCh38.p7	13:77290840	CACAGACTTAGGTGC[A/G]CACAAACACATACAC	23077
rs543430232	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77138107	AATTTAGTATTTTAC[C/T]TATAGATGTATCATT	23077
rs543434422	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77282403	CAAGCAGAGTGAAAC[G/T]CCATCTTGAAAAAAA	23077
rs543435965	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77145728	AAAAAGTCCTTAAAT[A/C]TGAAGTTAACAGAAT	23077
rs543447186	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77327333	TTCAGGTTCCCTCCA[A/G]GTGGAAGAACGAGGA	23077
rs543464281	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77298594	GGAAGTTGAGAGCTA[C/T]AGCTACATGCCTTAC	23077
rs543475597	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77064522	ATAATTATGTTGACT[C/T]AGTGATTAAAATTTG	23077
rs543481685	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77302414	AGTGGAGGGATGGGG[C/G]TTAGAGGTGGGGGAA	23077
rs543504292	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77267639	TGAAAACAAATATTA[A/C]AACTTGTTATATTTC	23077
rs543515976	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77055150	AAAAAAAAAAAGAAG[A/T]AGTAGTTAAAGATAA	23077
rs543519131	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77174228	TTTAATTATAAGTAT[C/T]CAGTTAGCAATTTTA	23077
rs543545018	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77126626	TAATAGCTTTTATAG[A/C]AAGTCTACAGTACTG	23077
rs543576639	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77165536	AAATAGACTTGCGGC[A/G]GGGAGCGTTCCTATA	23077
rs543596967	snp	A/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77049403	TTATCTTTATTTTGA[A/T]ATGGATAGTATATGT	23077
rs543605743	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77167409	CTGAAAGAACCAGCA[A/G]GTAAGCTGAAGAGGC	23077
rs543629165	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77305553	AATAGAAACTGACTG[A/C]TAATAGCTTTGGGAT	23077
rs543631081	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77321696	GATGCTTTTAAGCCA[A/G]CCTAGAATGCCATGC	23077
rs543636211	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77276151	TATTACATTTCAGTG[A/G]GTACTCGAGAATATA	23077
rs543644814	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77104259	TGCTGTTTTCGGCTG[A/T]TTCATTATTATGATC	23077
rs543651440	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77065830	CATAAATGACAAATT[A/G]TCACTCACTGAAAAG	23077
rs543654675	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77245090	CAATGGTGATCATTA[A/C]AAAGTCAGGACACAA	23077
rs543674636	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77314463	CTATCAAGTCTCATA[C/T]ACAAAAAAAGAATGA	23077
rs543677273	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77297931	TAACTCATTTCTGCA[C/T]ATCCATACCCTTCAA	23077
rs543679145	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77161044	TCTATCTTCACACCA[C/T]TGCTAGATGCAAAAT	23077
rs543689447	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77152958	TAGTCTCAGCTACTC[A/G]GGAGGCTGAGGCAGG	23077
rs543690560	snp	C/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77313012	GACAGAACATATCCT[C/G]GGCAATAAAACAAAT	23077
rs543715461	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77207052	ATACTTAATACAGAA[A/G]ATAGTAATGTAGATT	23077
rs543725975	snp	C/T	0.000399281	0.0141238	missense	MYCBP2	GRCh38.p7	13:77262087	ATTAGCGCAAACTCT[C/T]GTCCTGCACCAAGAA	23077
rs543730720	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77048707	AAAATGGAGCAAATA[C/T]GTGTGAAAATGCCCA	23077
rs543754782	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77198192	CCAAACTACTATTTT[C/T]CTTATTATCAAAATA	23077
rs543772739	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77308008	TATATTCACTTCTAT[A/C]CTGGTTAGTTACAAA	23077
rs543784490	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77089702	TCCCCAAAGTTTTAT[C/T]ATCTACTTAGAATGA	23077
rs543807697	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77149313	GAATTTGAATCACTG[C/T]ATATTTGTTTCAGGT	23077
rs543814011	snp	G/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77293223	ATGTGCTGGAAGGTA[G/T]AATTTATCAGAGGTT	23077
rs543817394	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77324855	CCATACACAAAATAA[A/T]TTTAAATTCTTTGAG	23077
rs543829204	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77190787	ATGCACATAACAACA[C/G]ATGTGATTTTTCTAC	23077
rs543855805	snp	A/G	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77185676	ACTATTACTTTTTGT[A/G]TCAGAATGACATGTA	23077
rs543861212	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77163704	ATATTCAAATGGACC[A/G]CCCTTCCTTACTTTC	23077
rs543864946	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77183702	GATTACAGCTGTGCA[A/C]CACCATGCCTGGCTA	23077
rs543867337	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77189858	ATCAGTCTTATGAGA[C/T]TACAATATATCAACC	23077
rs543869829	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77178458	TCATTTGAAGAAAAT[A/G]GTCTATACCCTAAGA	23077
rs543877711	in-del	-/AAT	0.000965581	0.0219513	intron-variant	MYCBP2	GRCh38.p7	13:77262043	TTTTAATCCAAAGAG[-/AAT]AATTTACCTTTCCAT	23077
rs543878569	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77240696	GAAACACAGAAATAC[A/G]GGAACTCTGTCCTCC	23077
rs543897112	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77194567	AACTCCAACAAAAAA[A/T]TTTAACTAAGTGAGT	23077
rs543897687	in-del	-/AGT			intron-variant	MYCBP2	GRCh38.p7	13:77160898	ACATTGCTGATAAAA[-/AGT]AGTACATTTTTAAAG	23077
rs543911906	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291365	CTAAAATTTAAAAAG[C/T]GAATACCATATGTTT	23077
rs543918804	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77100806	TGTTTTATAAATACA[A/G]TATTAACAGATGGGG	23077
rs543919429	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77286717	GCCGAGATGGCACCA[C/G]TGCACTCCAGCCTGG	23077
rs543932336	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77230673	ATTTGTATCCCTGCA[C/T]TATCAGAAAGCAAAG	23077
rs543937470	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77187586	TAATGGTACGCAAAC[A/G]GAGAAGACTGACAGA	23077
rs543944140	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77142207	TGTATGTCTTGTGTG[C/T]CACTACTTATATTCT	23077
rs543953992	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77045775	ATCTTTTTCTATTAA[C/T]AAATGCATCAGATAT	23077
rs543954686	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77080966	AAAAAAGCTGATTAC[A/G]CTATAGGTCAAAGAT	23077
rs543972108	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77242485	ATAAACAATAGACCT[A/T]TCTTTGCAAATGAAA	23077
rs543975773	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77175158	CCTAGCCTCAAACTC[C/T]CAAGCTCAAGTGATC	23077
rs544031198	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77287176	ACAGGCGTGAGCCAT[C/T]ACGCCCAGCCAGTTT	23077
rs544032593	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77126103	TTTATATATACAATA[C/T]AAATCATTTGTTAAT	23077
rs544040215	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77221969	TACCTAATACAATGT[A/G]AACACCATGTTAATA	23077
rs544042247	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77231675	TACTTGTCCATGAGA[C/T]ACTAACATGGAGCTG	23077
rs544053167	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77179234	GGAATTATAAAAGTA[A/C]AATAGAGAAAAGAAG	23077
rs544057838	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77270599	TACAAACACAGAACA[A/C]AGATACTTTGGTAAT	23077
rs544066165	snp	C/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77057958	TTCTCCTGACTCAGC[C/G]TCCTGAGTAGCTGGG	23077
rs544069264	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77272201	TCTTTCAGCTTTCAA[A/G]TATTTCACTCTTACT	23077
rs544091408	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77135063	TCTCTATAGTTTGTT[G/T]GAGTTGGGATCCAAA	23077
rs544101642	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77234546	CAAATTGTATGAAAA[A/G]CCATGAATAACATAT	23077
rs544134287	in-del	-/ACC	0.00557542	0.0525036	intron-variant	MYCBP2	GRCh38.p7	13:77126885	TACTATACTATGTGA[-/ACC]ACAAGGGAATAATTT	23077
rs544135787	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77170997	CTATATTAAAAAATG[A/G]AATGTACTTGCACCA	23077
rs544152093	snp	A/C	0.0283406	0.115616	intron-variant	MYCBP2	GRCh38.p7	13:77202379	TAGACCAATAACAGG[A/C]TCTGAAATTGTGGCA	23077
rs544157941	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77064382	TTTCTAACCAGTGTA[C/T]CCTTGGCTTCCTAAA	23077
rs544186982	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77311071	AAATTTCCCAGTTTG[A/G]TTGTTTTTCTCCTTT	23077
rs544203417	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77155036	TCCATCATATATTAT[A/G]TTTATATCTTTGGGT	23077
rs544203740	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77301802	TACCTGAGATGCAGA[C/G]ATTAACAATATGTGT	23077
rs544204271	in-del	-/T			intron-variant	MYCBP2	GRCh38.p7	13:77149387	GGGTGCTTGGAAATC[-/T]TTTTTTTTTTTTAAG	23077
rs544210900	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77164709	CTCAATGTTGTGGCT[C/T]AGGCTGGTTATAAGG	23077
rs544212573	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77093409	AATCTCTTTCATAAC[A/G]GGAAAAGCAGCACAT	23077
rs544218105	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77249610	ATGCTGCTGAAGCTG[C/G]TTTCAAACTCCTGGC	23077
rs544228960	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77283611	TTACTATTTAAAAAT[A/T]ATGCACCAGGCACGG	23077
rs544242440	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77176402	TAACTTACAAATAGC[C/T]ATAGGTAACAAACAA	23077
rs544250443	snp	A/G	0.00597247	0.0543191	intron-variant	MYCBP2	GRCh38.p7	13:77201539	AGCTCTGCACCAAGC[A/G]GACCTAATAGACATC	23077
rs544259155	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77266595	ATTCATTCTTTTTTG[C/T]TCATATGATTTTTAT	23077
rs544270108	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77092884	GCTCCCATGAAAACT[C/T]AAAGTAACCCTTCCC	23077
rs544297800	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77047646	GGGAACTAGCACAGG[A/G]CATTGTGCCTAAAGA	23077
rs544342050	snp	G/T	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77128428	GTGCATTTAATTAAT[G/T]ATAACAATAATTCTA	23077
rs544344324	snp	C/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77054528	GAGATGTAATGGAAA[C/G]AAAAAAGGACTCAAG	23077
rs544353113	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77241290	ATACCTAGAGAAGAA[C/T]AGCTTTTTTAGAGGG	23077
rs544363894	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77151108	ATTGAAAAGAGTTCA[A/C]ATGACCTCAAGATGG	23077
rs544377651	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77116717	AAAGTGGTGGTACTG[A/G]TAACACATATGCATA	23077
rs544382664	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77238007	CCAGCACTTTGGGAG[G/T]CCAAGGCAGGCGGAT	23077
rs544390178	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77069386	CCAGCAATTTGGGAG[G/T]CCGAGGCGGGCGGAT	23077
rs544394925	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77197470	TGAATTCAGTTGAGA[C/T]ATTATGACTGATAAC	23077
rs544416398	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77250397	GAAGGTCAAGAGGCA[A/G]GGATGGCTGTCTTCC	23077
rs544420752	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77225325	TTGAGAGACTGCCAC[A/G]CTACAGCTTTTAACA	23077
rs544422598	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77053575	GCTGTTTCACTTTTC[C/T]ATATCCTCTGCTTGG	23077
rs544429112	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77157772	CAAACAAACAAACAA[C/T]CGCCAAACAAAAATA	23077
rs544430214	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77235308	CAGGACAATCAGCAA[G/T]GTTTCAAAGAATGAC	23077
rs544462466	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77265855	TTATCCATCATGTAA[C/T]ATTTTAAGCTTGTAT	23077
rs544468260	snp	C/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77164070	TATTCAATTACATTT[C/G]TATCGACCTGTTCTC	23077
rs544470506	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77218538	ACTTAATAATAATGC[A/G]ACCAGACTTCGAACA	23077
rs544476307	snp	A/G	2.66273e-05	0.00364869	synonymous-codon	MYCBP2	GRCh38.p7	13:77296646	TCTGTTTTCTTTTCA[A/G]TTTCTTCTTATTTAA	23077
rs544490159	snp	A/C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77303941	GGGAGCCAAAAATTG[A/C/G]TTCTCTGAAAAGATT	23077
rs544500989	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77273042	CTCAGAAACGAATCA[A/G]TTCATAAAAAAATCA	23077
rs544511620	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77117791	TAATTTTTTTGGGTA[C/T]CTTTTCCAAACCAAT	23077
rs544543620	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77064149	CCTGACCCTGCCCTG[G/T]ACAAGCACTTCTTGC	23077
rs544545553	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77180914	GACAGAATGAGCTAG[A/T]CTTAAAAAACAAAAA	23077
rs544566044	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77237186	ATAAACTATGGTATA[C/G]CCATATTATGATATT	23077
rs544567442	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77135129	TTAACTAGAAAAGGT[G/T]GAAGAGATAGACACA	23077
rs544587616	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77110470	GTGCACAGCTGAACA[C/T]AGACCCTCATCAGTA	23077
rs544592379	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77323798	AATAGGATATGATGC[C/T]TATCCTCAATAAACT	23077
rs544593141	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77211556	TATAATTATTCACAG[C/T]ATCATGGACACAGTA	23077
rs544604766	snp	A/G	0.000585093	0.017094	synonymous-codon	MYCBP2	GRCh38.p7	13:77243921	TCCACACACAGCACA[A/G]CCAGATTCTCCGGAA	23077
rs544605116	snp	C/T			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77229036	TTTACTAAGCACTTG[C/T]TGTGTGCTAACTGAA	23077
rs544607225	snp	A/G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77157244	CACCATGCTTGGCTA[A/G/T]TTTTTGTATTTTTTG	23077
rs544620622	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77242621	GCAGGACTATGTCCA[A/G]ATGATAATGAGCATA	23077
rs544621077	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77115638	TTAACTTAATGTGCC[A/G]GATTATTTTCAAATT	23077
rs544628856	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77134332	GCCAGGAGTTCGAGA[C/G]CAGCCTGGCCAACAT	23077
rs544634015	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77211035	TGTGAATCACTGAGA[C/T]AGAATTGCAGTTATT	23077
rs544664802	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77303468	AATAGATAATATGCT[A/G]GACCACAGACCAAGT	23077
rs544666316	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77226749	TATTACTTTCCTTTC[C/T]GTAACTAAATGCCTA	23077
rs544670281	snp	G/T	0.00119737	0.0244387	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77086279	TTTTAAACAAACTCA[G/T]TATTTTAACTTGTAA	23077
rs544694372	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77072370	TGAATTGAATGAAAA[C/T]AAAAACAGAATACCC	23077
rs544701567	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77094415	CCACATTAGCTTCCA[C/T]ATTCCACAGTGATTT	23077
rs544705075	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77255335	CTCATCTGCTTTCTA[A/C]TTCATTACTTACCAG	23077
rs544714810	snp	A/G	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77280048	GTAGGCACACATTAA[A/G]TATTTGTTTAATTTA	23077
rs544720086	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77268957	TGCAGGGAAATCTTT[A/G]TTCTTTATCCTTATA	23077
rs544730990	snp	A/C	0.00993419	0.0697739	intron-variant	MYCBP2	GRCh38.p7	13:77069661	GGAGATCGAGACCAT[A/C]CTGGCTAACACGGTG	23077
rs544768409	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77288090	AGTATTTTAGCAATG[C/T]GTATATATGCATTAT	23077
rs544776554	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77144134	GCTCACAGTCAGGAG[A/T]GGCACAGACACACCC	23077
rs544789609	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77287825	CACTGGCTCAGAGCT[C/G]TACTTCCATCTGCCA	23077
rs544794907	in-del	-/C			intron-variant	MYCBP2	GRCh38.p7	13:77119026	ATAAATTAATACTTT[-/C]TTTTTTAAGTTGTTA	23077
rs544824770	snp	A/C	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77051296	AAAAATTGATTGAAA[A/C]ACTGATGATACACAT	23077
rs544834302	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77251567	AAAGAAGGCAAGGAA[A/G]GCTATTGTCAAATGT	23077
rs544852256	snp	A/G	0.000101293	0.00711592	intron-variant	MYCBP2	GRCh38.p7	13:77070723	TTGCCTTTACATAGA[A/G]AAAGAAAAAAAAAAA	23077
rs544857024	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77296212	ATTGCTTGAGCCCAC[A/G]AGTTCGAGACAAGCC	23077
rs544864641	snp	A/G			upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77327996	GCTCTAGAAATATAC[A/G]TGCCAATGCACTTTG	23077
rs544874072	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77157808	TATCATTTTATATTT[A/C]AGCAAGTTAAACATA	23077
rs544885645	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77227329	TGCCAAATTAAATCA[A/G]AGAATGGATGGACTA	23077
rs544892886	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77180480	GCCACTTTTCACTTA[A/G]AAGTTCTTTTTTGAA	23077
rs544898684	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77294657	ATACTCCGATTTGCA[A/C]ATAGCACCAAAAAGT	23077
rs544917222	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77136785	TCAACCTCTTCCCTT[C/T]GTCCCTCCCTCCTCT	23077
rs544918512	in-del	-/TTTTTTT	0.132066	0.220435	intron-variant	MYCBP2	GRCh38.p7	13:77057835	ATTTCAATCAACTGC[-/TTTTTTT]TTTTTTTTTTTTTTT	23077
rs544919536	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77121169	CTCATAAACTTAAGC[C/G]AAAACTGGTTAAAAA	23077
rs544934593	in-del	-/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77115821	GACATTCAGGAAATC[-/T]TTTTTTTCCATTCAA	23077
rs544937365	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77288620	GATGGGCAAAAAACT[G/T]AGAAATATTCTTGTA	23077
rs544938038	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77319153	TCCCTTCCTCCCTTC[A/G]CAGATCCAGCACCCC	23077
rs544959356	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77197145	TGAATTTAGCAATAT[C/G]AAAGTCATCAGTGTC	23077
rs544985922	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77120887	TCATTTCACATAATT[A/C]TAAATTAACTAAGAT	23077
rs544987710	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77287234	TCTGTCACCCAGGCC[A/G]GAGTGCAATGGCATG	23077
rs545002108	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77295049	GGAGTTGGAGCTACT[G/T]GCAGCCTCAGCCTCA	23077
rs545004325	snp	A/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77303552	ATTAAACGAGAAATT[A/T]AAAAAAAACAAACAA	23077
rs545010898	snp	A/G	0.000241221	0.0109796	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076741	ATATCTTTAGAATAC[A/G]AATAAATACATTGTA	23077
rs545014234	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77222772	TCACTAATCTTTACC[-/A]ATGTAAATGGCAGAA	23077
rs545017460	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77163332	AAGGTCTCATTTCCA[C/T]ACATATATACCAATA	23077
rs545035877	snp	C/G	0.000232153	0.0107714	intron-variant	MYCBP2	GRCh38.p7	13:77205442	ATATTTCAGTTGTAA[C/G]ACAACATTTCCTAAA	23077
rs545038589	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77288514	GAGACAGTCTAAGTC[G/T]ATGGACCCAACTTCT	23077
rs545052309	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77252202	TTCACGGCAAGAAAT[C/G]AGCAAACCTTTTATA	23077
rs545053320	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77259330	CAATACCACTTCCCC[A/G]ATATTTAAGTTCTGT	23077
rs545068372	snp	C/T			synonymous-codon, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076787	TTCAGGTGATGACAA[C/T]AGTGCTTTTTCCTCT	23077
rs545073995	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326022	AATGTCATGGGAGAG[A/G]CGGCACGTGCAAATA	23077
rs545075320	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77312166	TCCTTTAGGAATGAA[A/C]GTAAAATAAATACAT	23077
rs545086013	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77126283	TACATTAAAAATGAG[C/T]ATCTTAGAAGTCATG	23077
rs545086701	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77047745	CTTTGTCCTTTGTAT[A/G]GTCAGGGGGCTCTCT	23077
rs545094292	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77179438	TTAAGTTATAAGAAA[G/T]AGTAAGGCAGTGAAA	23077
rs545094463	snp	A/G			intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77074379	TAAAGGAAAAGAAGA[A/G]AATATCTGTGTGACC	23077
rs545101855	in-del	-/T	0.334642	0.235236	intron-variant	MYCBP2	GRCh38.p7	13:77287192	CGCCCAGCCAGTTTC[-/T]TTTTTTTTTTTTTGA	23077
rs545172092	in-del	-/G	0.00159904	0.0282305	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228695	AGATGAATATGTTGT[-/G]TGTGTGTGTGTGTGT	23077
rs545185390	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77079297	TTATGAGTGTCACAA[G/T]GTACCCAGACTTCCT	23077
rs545191387	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77189607	CTTAACGAATGACAA[C/T]ATTTTTCAGTAACGG	23077
rs545228411	snp	A/C	1.70519e-05	0.00291987	intron-variant	MYCBP2	GRCh38.p7	13:77189070	CAGTAGACACATATA[A/C]AATTATGTTAGAAAG	23077
rs545232814	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77218660	GTAAAGAGGCCCATA[C/T]GTGTCAAGTACTTGG	23077
rs545244971	snp	A/G	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77323103	TACATTGATTCATTT[A/G]ATCTACAAAACAATT	23077
rs545246765	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77196544	TTCAGAAGTGGTTAG[A/C]TACGGGATTTATTTT	23077
rs545248489	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77328129	TTCATCTATGTACTA[G/T]TTCTTATATCTGTGC	23077
rs545254358	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77258884	TGCAGGTAGAAAAAA[A/C]CAAAAAGAAAACTCT	23077
rs545259179	snp	A/G	0.0146672	0.084371	intron-variant	MYCBP2	GRCh38.p7	13:77072304	TCAAAAAAAAAGAAA[A/G]AAAAAAAAAAAAAGA	23077
rs545261481	snp	A/G	0.000798403	0.0199641	utr-variant-5-prime, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326867	TTTTCCAACGACGAC[A/G]GCTCCGGCGGCGGCC	23077
rs545270218	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77289606	TAACATGGTAATAGA[C/T]TGAATGCTTTCCCTC	23077
rs545281919	snp	A/G	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77298996	AATAAAACACAATAC[A/G]TATTCTTCATACTAT	23077
rs545291121	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77266860	TATTTCTGAAATGGA[C/T]ATGAAATGTCATATT	23077
rs545310470	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77212235	AAGTTAAGGAGGCAG[C/T]AGATAAAAATCAATC	23077
rs545324351	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77130592	AATTAAAAGTGGATA[A/G]GGAATACGTCCTTTC	23077
rs545325302	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77110702	CAGAGGCCCAGCTGT[A/G]AAATTCCTCTTTGTA	23077
rs545348110	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77173413	GTAACAGAAAGCTTT[C/T]CTTGACTGGGGCAAA	23077
rs545353233	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77199567	GGCCTGCCTGCCTCT[A/G]TAGGCTCCACCTCTG	23077
rs545373412	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77229744	ACATTTTGCACAGCC[A/T]TGTAGTTCTAGTAAA	23077
rs545388030	snp	C/T			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076558	GCAAATTTGCTGTTA[C/T]TTAAAATACTAGCTA	23077
rs545393052	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77151164	GTGTAAAAACAAGGC[C/T]TCATAGTTTTGGAAT	23077
rs545397534	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77314850	TGGATGAGGCTATGC[A/G]TGAGTGGGGGAAAGG	23077
rs545400453	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77103982	TGTTAGGAACGTCAA[C/T]GATTTACTATGCAGG	23077
rs545404824	snp	A/C	0.00676609	0.0577691	intron-variant	MYCBP2	GRCh38.p7	13:77096082	AAATATTTGTCAATA[A/C]GGCATATGTAGCAGA	23077
rs545405614	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77050834	GCCTGCTTCCTAATT[C/T]ACCCAGAAAGTCATA	23077
rs545408003	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77237841	CTCTAAATTCTTCAT[A/G]TAATACTTTAATTTA	23077
rs545423661	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77319683	GCACTCACCAGTGCA[C/T]TCCCTTCAACAGGAA	23077
rs545434567	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77203787	CCTGAGAAAAACAAG[A/C]AATGGGGAAAGGATT	23077
rs545466644	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77212549	GACATAGTAAGTTGA[C/T]AGTATAAAAGAAAGT	23077
rs545481568	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77298035	ATCAGTATCTTCTCA[A/G]TTCTCTTAAGATAAA	23077
rs545487982	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77153865	TCAGACACTGATGGT[A/G]CTGAACCAAAACCAG	23077
rs545515038	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77199922	AAGACCAAAAGTCGA[C/T]AAAACCACAAAGATG	23077
rs545530441	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77143730	ATTGTGCAAACATCA[A/G]AGTGGACTTAAGCAA	23077
rs545536054	snp	C/G	1.6615e-05	0.00288223	missense	MYCBP2	GRCh38.p7	13:77095395	GACAAGGCATTTTCA[C/G]AGGAAGATCCTCAGA	23077
rs545541332	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77051302	TGATTGAAAAACTGA[G/T]GATACACATGTTTGA	23077
rs545560443	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77251733	TCATCCTCCTACTGC[C/T]ACCAATCACCCTCCC	23077
rs545563101	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77139393	AGTCCTATGAGGCTA[G/T]CAAGGTCTGAAAGTC	23077
rs545578781	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77128885	TCACCTAAATAAGTT[A/C]GTTGTGAAAACACTA	23077
rs545578858	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77137792	ACGGGGTTTCACCAT[A/G]TTGGCCAGGCTGGTC	23077
rs545581206	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77281736	TTTCAAGGTTTTATT[C/T]TGCCCTTCTCAAATC	23077
rs545584686	snp	A/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77194327	TAATTTTGTGCATGA[A/T]GAATGTATGCTGGAC	23077
rs545606428	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77300024	TCTATCAGCTTATTA[C/G]TGAGTATACTTTATA	23077
rs545624652	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77146607	TCCATACAAAAGAGA[A/T]AAACAACAACAAAAA	23077
rs545635991	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77244762	AATTTTTGCAATTTA[A/C]TCATCTGACAAAGGG	23077
rs545640321	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77136859	AGCAAGCTCTCTAAG[A/G]TGCCCTTAATTCCAT	23077
rs545689194	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77275522	CATCTTCAGGGAGCC[C/T]GTTAAAGACTCTCAG	23077
rs545691878	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77172761	GAATATTCTAGCCAC[A/G]TGAAACCTCAGATGT	23077
rs545696251	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77239629	AGAATCACCTGGAAC[G/T]CTATTAAAGCACAGT	23077
rs545716413	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228828	ATAATTATATACACA[C/T]ATTTGTATACACAGA	23077
rs545766434	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77216431	GAGAAGCAGGCATCT[C/T]AAAAGTGTCAACCTA	23077
rs545774237	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77123910	AAATATACAGCAATA[C/T]ATAATAAGCACATAG	23077
rs545778997	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77092766	TGTAACAAGTTTCTA[C/T]TCAGCTTTCCGAGAA	23077
rs545784384	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77176400	GATAACTTACAAATA[A/G]CTATAGGTAACAAAC	23077
rs545785618	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77123478	ATCCTTAGCATGGAA[A/G]GCATTTTGCATTTTA	23077
rs545832583	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77215366	GGTGGGAGGGGAAAG[A/G]GCAAGAATGACCTTT	23077
rs545853912	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77316212	TAATAAATGAGCTTA[A/T]CAAGATCAGAGATAC	23077
rs545864880	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77179595	CCACTGAACTGTACA[C/T]GTAAAAATGATTAGA	23077
rs545865418	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77147338	CTGTTTCTTAATAAA[A/T]AAATAACAAAATGAC	23077
rs545868706	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77247641	AAAAAGAAGAACAAA[C/G]TACTCGGTTTTGACT	23077
rs545897519	snp	A/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77108711	AGATACTTTATTTTT[A/T]TTTTTTTTTTGAGAT	23077
rs545921038	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77323651	GTGGATTTTCCAAGA[C/T]GGCAGAGACTTTGTC	23077
rs545926645	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77154972	ATGTGTGTATGTATA[A/T]ATAAAGTATATTATA	23077
rs545928788	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77154532	AGATATCAAAAGAGA[C/T]AATAAAAGGTGCAAA	23077
rs545955996	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77060495	TCGTGTCAGTCAAAT[C/G]GCAGACTGCAGATGT	23077
rs545965824	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77101041	AGATTAAATCAGTAG[C/T]CATGGCCATTAATTT	23077
rs545968008	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77210319	TGCCTCAGCCTCCCG[A/G]GTAGCTGGGATTACA	23077
rs545971002	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77284927	TAGTAATTTTAATGG[G/T]GTTTGAACCCCAGCA	23077
rs545977098	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77141070	TGATTTCTGTCCTTT[C/T]AAGGTGATGGATATT	23077
rs545978745	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77131870	ATAATCTTTCATGGC[A/G]TAGAAAAGAGACCAA	23077
rs545984416	snp	C/T	3.73853e-05	0.00432334	intron-variant	MYCBP2	GRCh38.p7	13:77264034	GTATTTATATTACAA[C/T]ACAAGCAAACACCTT	23077
rs546029151	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77109106	AGTAGGGAAACTGTT[C/T]CATTGTTTCCTTTAT	23077
rs546043424	snp	C/T	0.00755907	0.0610114	intron-variant	MYCBP2	GRCh38.p7	13:77250055	GGTGAAACCCCGTCT[C/T]TACTAAAAATACAAA	23077
rs546083769	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77185500	AATATCTTAGAAATG[A/C]AACAACTTAGAGATT	23077
rs546106263	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77240472	AATTAGCCAGGCGTG[G/T]TGGCGGGCACCTGTA	23077
rs546107564	in-del	-/ATC	0.0225045	0.103662	intron-variant	MYCBP2	GRCh38.p7	13:77204769	TGGATGAAATTGGAA[-/ATC]ATCATTCTCAGTAAA	23077
rs546115231	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77132963	TATGCAATCAAAGAA[C/T]AACTCATGTCATCTT	23077
rs546131365	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77285859	AAGGAGAAAGGAAGG[C/G]AAAGGAAAGGAAAGG	23077
rs546131871	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77249667	CCCAAAGTGCTGGGA[C/T]TACAGACATGGGCCA	23077
rs546134216	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77094260	AGCTGATGAAAAAAA[C/T]TTGGTTTTGGTATAT	23077
rs546150994	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77115891	AAATAATCAATCTGA[A/G]CAAAGCTAATACTCT	23077
rs546159206	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77324772	GATACACAGAAATCA[C/T]ATTACACTAGTAGTA	23077
rs546164342	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77108637	TGAGAAAGAGACAAC[A/G]CTTACGCAGCACAAA	23077
rs546177507	snp	A/T	0.00874735	0.0655527	intron-variant	MYCBP2	GRCh38.p7	13:77068460	TAACAAAATACGAAA[A/T]AAAAATCTATACTTA	23077
rs546180810	snp	C/G	0.000399281	0.0141238	intron-variant, missense, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77292284	TGCTTGCTCTGTATC[C/G]TTTGTTGTAATAAAT	23077
rs546191255	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77272949	GATTATTTTTCCCAC[C/T]ACTAAAATGGTGATG	23077
rs546201934	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77202269	TACAAAATCCTCTAC[A/G]CAAATAAACTAGAAA	23077
rs546205923	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77294557	CTTGACTTCTCCTCA[C/T]CTCTTCCTGGATATC	23077
rs546233098	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291639	GGGCGTGGCGGTGCA[C/T]GCCTGTAATCCCAGC	23077
rs546233374	in-del	-/T			intron-variant	MYCBP2	GRCh38.p7	13:77189979	AAATCAATGGATAGA[-/T]TTTTTTTTAAAGTCA	23077
rs546242596	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77316770	GGTGGCTGACTTCAT[C/G]GGGTGGTCACTGGGC	23077
rs546242762	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77264526	TGTTTATTCACAGCA[C/T]TTTTAGCATTTAGTG	23077
rs546292854	snp	C/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77052233	AGACGGGCTCTCACT[C/G]TGTTGCCCAGGCTGG	23077
rs546314300	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77059232	GTGAATAATGTCTGT[A/T]AGAGATAAAGGAAAT	23077
rs546314514	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77184622	TCAATGTGAATCTAT[C/T]TCTCCCTGTAGTTCT	23077
rs546332234	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075299	TACAGTTTAAAATGA[C/G]GAATTTCTGTATGTA	23077
rs546336515	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77201608	TTTTTCAGCACCACA[C/T]CACACCTATTCCAAA	23077
rs546351708	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77162422	TTAATATAGAACATA[C/T]TTTATTTATTGATCT	23077
rs546370434	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77045904	TGTGTAGAATGTTTT[C/T]CTATAAGTAAAAACA	23077
rs546370663	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77222947	CACTGTGACTGCGAG[A/G]AAGAATAAGGCAGAG	23077
rs546373396	snp	A/G	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77281629	ATAAAGAAACATGAA[A/G]CCCAAATAATTACCT	23077
rs546387668	snp	C/T	3.35542e-05	0.00409585	synonymous-codon	MYCBP2	GRCh38.p7	13:77156178	TGTTTTCTGAGGATC[C/T]GCATATGAATCTGGC	23077
rs546404208	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77246589	GGAGGAAAAGAAGGA[A/G]AAGGAGGAAGAGGAG	23077
rs546407269	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77301836	ATAATGCAATTGGCA[A/G]TTTTCAACATAATTT	23077
rs546409257	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77310394	ACATGCCAAAAACAG[A/C]TTCCTGTCTATCTTT	23077
rs546425167	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77323065	GTAACTAATATTTCA[G/T]AGCAGTCAACATGCC	23077
rs546431593	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77052825	CATCCTCTGATCACA[C/T]ATTTTTTAAGAAGAA	23077
rs546439679	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77188645	ATCCTTAACTTTTCC[C/T]TCATTTTCTAATTCA	23077
rs546468044	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77216835	CAAAAAATAATTATT[A/T]GGTCAATTCACAAAA	23077
rs546476781	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77163107	GCCATTACTTATTTA[A/T]CCAGTTCCCAACTGA	23077
rs546509167	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	MYCBP2	GRCh38.p7	13:77045320	AGTTTAAACTTCACC[A/G]CATCCTCTTGGGGGA	23077
rs546512884	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77323781	TTGGGATTATCAAAA[C/T]GAATAGGATATGATG	23077
rs546521019	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77058933	GAGGTTGCAGTGAGC[C/T]GAGATCGTGCCACTG	23077
rs546530492	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77162679	TTTTTTCTTTTGAGA[C/T]GGAGTCTCACTCTGT	23077
rs546534400	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77308394	TAGGTTAAGAGTACA[A/G]AATTTAGAAACAAAT	23077
rs546550800	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77256123	TATTGTGAAGAAGGT[A/G]TGTCTACAATTTAGT	23077
rs546553258	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77082501	AATTAGGAGAATTTA[C/T]TTATAAGTGTGAGTC	23077
rs546573847	snp	C/T	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075467	TCTCTGATCAGTCCT[C/T]GCTCCCATTCTCTCT	23077
rs546597793	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77315243	AACAATCTTACGCAA[A/T]CATTTTAAAAATTGG	23077
rs546611403	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77237350	ACACTTTCACATATG[C/T]GTAAGTCTCTGTACA	23077
rs546616980	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77201950	GAAGCAGGAAAGATC[C/T]AAAATTGACACCCTA	23077
rs546623496	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77099615	ACATGAATGCCCTGA[A/G]GCTGTTATTTAATTA	23077
rs546631469	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77210342	GGATTACAGGTGCCC[A/G]CCACCACGCCCGGCT	23077
rs546649968	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77241014	GCAGATGAAACCTAT[C/T]TGTCACAAAATATAC	23077
rs546654127	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77235480	AGAGTATATGTGATG[C/G]AGCAAAAGTCTTGGG	23077
rs546667122	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77175007	GTCACCCAGCCTGGA[A/G]TGCAGTGGTGCAATT	23077
rs546692577	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77232639	TGCACTTATCTCTAC[A/T]TAACCCACAACCATC	23077
rs546698997	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77093078	CTCACAGATGTATTA[A/T]AGAACTTCTACAGGA	23077
rs546716417	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77200266	GCCTCAGGAGCCGAT[A/G]AGATCAACTGGAAGA	23077
rs546739364	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77249681	ATTACAGACATGGGC[C/T]ACTACACCCAGCTAA	23077
rs546750494	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77169170	TCCCAGCACTTTGGG[A/T]GGGCGAGGCGGGCGG	23077
rs546751863	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77239740	CCAAGTGATGCTGGT[C/T]CCTTTGAGACCACCT	23077
rs546771527	in-del	-/A	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77274828	ACTTAAAATTCTTTC[-/A]CTCCTTTGTTAATTT	23077
rs546831913	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77124145	ATTTAAAACACGAAT[A/G]AAGATTCTGGCTGAA	23077
rs546832122	snp	C/T	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77316315	CTAGTTACAGTAGCA[C/T]TAAAAACCATAAAAT	23077
rs546840585	snp	G/T	1.66776e-05	0.00288765	intron-variant	MYCBP2	GRCh38.p7	13:77051804	TCTAATAAAATGTTC[G/T]GCCTACCTGAGCCCT	23077
rs546863617	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77085904	TGGGGTAGTTATGCA[A/G]GAACAGATAGCTGTT	23077
rs546869921	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77125711	AGCACAAAGATAACA[C/G]CTAAATAATTTTAAG	23077
rs546871140	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77108381	TGAGCATAATTTGAT[C/G]GGTATATATCTTAGG	23077
rs546884031	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77142358	CTAAAGGCTTTATGA[A/G]TATATTGAAATAAAG	23077
rs546885630	snp	C/T	3.33723e-05	0.00408473	intron-variant	MYCBP2	GRCh38.p7	13:77161980	AAATAAAGAGTTTTA[C/T]TAAAATATGTCAATA	23077
rs546919066	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77268672	TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAAG	23077
rs546922492	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77286209	TCCATTTATGCTGCT[A/G]TTTCCAAGTAGTAAA	23077
rs546923382	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77234953	TAAATTCAATCTTTT[C/T]AGAATCTTTTGATTT	23077
rs546926137	snp	C/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77201033	ACAGGACCAAATTCA[C/G]ACATAACAATATTAA	23077
rs546929377	snp	A/G			intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77074969	ATCTCAGCACTTTGG[A/G]AGGCCAATGCTGGCA	23077
rs546931328	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77125104	AAGCCTGTTTTATAA[A/C]GATGAGTCTATATGT	23077
rs546939288	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77107123	TGGGAACAGTGTTGC[C/T]GACTTTCCTCAGCTT	23077
rs546959008	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77256795	GAGAATGTAAATTTA[G/T]TACAGCCACTCTGGA	23077
rs546963477	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77289165	CCAAAAACACTTGGT[C/T]CCAAATATTCGACTC	23077
rs546997887	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77301336	CAGGAGAATCGCTTG[A/G]ACCTGGAAGGCAGAG	23077
rs546998825	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77213054	CTGAGCTTCAATCCC[C/T]GGACAGAACCAGGGA	23077
rs547000307	snp	C/T	1.64972e-05	0.00287199	missense, nc-transcript-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076825	GTGTAGGTTCAGCAT[C/T]TCCAGAGATGAGCTT	23077
rs547004242	snp	A/G	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77155551	TTTCAGGTAAGAGGT[A/G]TCCTAAAAACTCTAT	23077
rs547005873	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77147867	GTGAATGGTTGATAA[A/G]GAAAATTTCCTTTCC	23077
rs547015351	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77103581	TCTGATAAATCAAAA[C/T]TGAGCATTTCATTTT	23077
rs547019514	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77218377	TTTTATGATCATCTT[G/T]TCTAACTTTTATCAC	23077
rs547020886	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77134494	AGCCAAGATCGTGCC[A/C]CTGAACTCCAGCTTG	23077
rs547048487	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77244454	TGCTGGGAAAACTGG[A/C]TAGACATATGCAGAA	23077
rs547056460	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77213941	GCTACTGCAAACCTG[A/C]GCATGTGCAAAGCAC	23077
rs547056580	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77247272	GTAGGAAGATACAAA[A/G]TCAACACACAAAAAT	23077
rs547059806	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77259725	AAACTTCATTAATTC[C/T]AGTTTCCTTTTTTAC	23077
rs547066873	in-del	-/A	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77118234	GATAACATCCTAATT[-/A]AAAAAAAACCAGTCA	23077
rs547085302	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77302049	GAACCAAACAGAGAA[C/G]GAGACATGTGGGACA	23077
rs547094099	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77245376	CTCATCAATGATAGG[C/T]TGGATAAAGAAAATG	23077
rs547096868	snp	C/T			downstream-variant-500B	MYCBP2	GRCh38.p7	13:77044387	ATAAAGTTAAAAATG[C/T]TGCTAGTTAAAATAG	23077
rs547118914	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77312414	GATGTTTGCCAAGTA[C/T]AGTATGCATGACAAC	23077
rs547127538	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77286963	CATCTCGGCTCACTG[A/C]AAGCTCCGCCTCCCG	23077
rs547142397	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77148843	CCATCCCAAAACACA[C/T]AATTACTGTTTTAAA	23077
rs547161798	snp	A/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77197794	GAGGTGAAGGGAAGG[A/T]AAAAAAAAGACTGAC	23077
rs547184280	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77276720	CAGCTAGAGTGCAGC[A/G]CAGTGGCATGATCAC	23077
rs547190080	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77137173	TGACCTTAAGGAGAC[C/T]GTCTACTACAGATTG	23077
rs547193237	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77135475	TGCACAGTCAGATAC[C/T]CATAAAAAAAATGTA	23077
rs547203731	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77177980	TAAAAGCAATTGTAT[C/T]AGTAGTTGGTATACC	23077
rs547208347	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77245140	GGAGAAATAGGAACG[C/T]TTTTACACTGTTGGT	23077
rs547220919	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77084751	GCTTACAATTCATTT[C/T]CACTGCTAGATCCTC	23077
rs547240724	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77186193	GAGTTTTTTAATTGA[A/T]TTTTTTTTACTGAGC	23077
rs547254506	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77079605	GGTTGAGGAACATGG[A/C]GGTACATAACTCAAG	23077
rs547264542	in-del	-/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77163086	ATACTACCATTGAAT[-/G]GCTATGCCATTACTT	23077
rs547268439	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77129927	ACTTTTCTCTATCTC[A/C]AAGTTTAGGAAATGC	23077
rs547270294	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77169476	GAGAAGTTTAATAAT[C/T]AGCAGATCTATCTCT	23077
rs547273348	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77069419	TGAGATCAGGAGATC[A/G]AGACCATCCTGGCTA	23077
rs547289950	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77279640	GTAGAAACTCCCAAA[A/G]CCATTAATTCTATTG	23077
rs547301556	in-del	-/TTA	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77072991	TTTTTAAAAACATCT[-/TTA]TTGAGATATAGTTCA	23077
rs547307120	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77325378	AAAAGATGAAGCCAA[C/T]TCCCAATTACCACTG	23077
rs547313390	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77178650	TTCTAATCTAACTTG[G/T]CTACAGAATTTTGGG	23077
rs547371408	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77055323	ACTGATGGGAAGCAG[A/C]TTGTATACAGAAATA	23077
rs547378376	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77048848	CTCAGCTACTACCCA[C/T]CACTGAGTTCTCTAA	23077
rs547382926	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77268616	TAAACCCGTCTCTAC[C/T]AAAAATACAAAAATT	23077
rs547382979	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77276386	GTGATATTAGATTAA[A/C]AAAAGGAGGAGAGGC	23077
rs547408465	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77158797	CATGAGTAAGGTGTG[C/T]CTGTTCTCTTGGGTG	23077
rs547412383	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77107795	AACAGTGATGATTTG[C/T]ATATACTCTTAGCTA	23077
rs547419855	in-del	-/C			intron-variant	MYCBP2	GRCh38.p7	13:77141770	AGTGAGACTCTGTCT[-/C]AAAAAAAAAAAAAAA	23077
rs547428534	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77253154	GTAAAAAAGCTCCTA[C/T]AAATCAATTTTTAGT	23077
rs547430515	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77207337	TAAACAGTAAAAACC[A/G]ATTAAAAACTATTAG	23077
rs547441280	in-del	-/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77092694	GCCTCCCAAAGTGCT[-/G]GGATTACAGGTGTGA	23077
rs547451307	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77166636	TGTATGTGTGTGTGT[A/G]TCTATGCTTTTATTA	23077
rs547461290	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77070930	TCAGAGAAGTATATT[C/T]TCCTTTCACAAATTT	23077
rs547481624	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77305761	ATCAACATAATTCAA[C/T]ATAATAACAGAACAA	23077
rs547483684	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77297447	ACTGCTGTAATAAAG[A/G]AAAAAGGATGAAGTC	23077
rs547492923	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77269302	TCTGTGGTAAGAAAC[C/T]CTAATTTGGCCTCAG	23077
rs547504894	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77247808	GCCAAGATGGTTCAA[C/T]AGAGAAAGGATAATC	23077
rs547509472	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77173781	TTAACCCAAGGGTTG[C/T]TATCATTCTTTTATT	23077
rs547519811	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77284298	AATGGGACAGCCACA[C/T]ACTTAGGAGGAGCAA	23077
rs547532018	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77314046	AGGAACTCTCATTTA[C/T]TGCTGGTGGAAATGA	23077
rs547573661	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77153448	TCAAGGGAACTCTCC[C/T]GTCTCAAACATATTT	23077
rs547574156	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77145016	CAATTTAGTGAATCA[C/T]TTCGATTAGCACACA	23077
rs547579795	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77084320	ACCAATGTAAGCCCA[C/T]CAAACTTTTTAAACT	23077
rs547615534	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77289178	GTCCCAAATATTCGA[C/T]TCTTCTTCCATAAAG	23077
rs547615688	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77274493	AGAGGGAAAGGGAAG[G/T]GAGAGAAGGAGGAGA	23077
rs547617359	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77298061	ATAAAGTCCAAAAGC[A/G]CCGACATCGTTTAAA	23077
rs547617965	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77088420	TATAGGCCTGTAATA[C/T]ACAGTAATCCTATTA	23077
rs547627651	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77199158	CTAGGGAGTGCCAGA[C/G]AGTGGGAGCAGGACA	23077
rs547653521	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77299501	TTTCTAAAAGAGCCA[A/G]TAATAAGTTGAAAAT	23077
rs547655207	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77135492	ATAAAAAAAATGTAC[C/T]GACTGCGTAAGGGGT	23077
rs547719122	snp	A/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77306763	GCCTCAGAGAACAAC[A/T]AGAGGAATGAGAGCA	23077
rs547729825	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77072038	TCACGCCTGTAATCC[C/T]AGCACTTTGGGAGGC	23077
rs547737004	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77222006	ATACTCTGTTGTTTA[A/G]GAAATAATAACAAGA	23077
rs547741500	snp	C/T	5.02063e-05	0.00501005	intron-variant	MYCBP2	GRCh38.p7	13:77139156	CTGTAAAACAAACAG[C/T]GTGTATCTATAATGC	23077
rs547751393	in-del	-/TTT	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77055130	TATGTAAGGGGTAGG[-/TTT]TTAAAAAAAAAAAAA	23077
rs547754459	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77096956	ATGCAGTCTTCTGAT[A/T]AAACAATATCACTTC	23077
rs547800917	snp	C/T	1.6656e-05	0.00288578	missense	MYCBP2	GRCh38.p7	13:77146207	TCTTCAAATGAATAA[C/T]TTTCATAAACCTTTA	23077
rs547803689	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77283675	GCTGAGGCGGTCAGA[A/C]TGCTTGAGCTCAAGA	23077
rs547806154	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77065376	CATGATTTAAGGGGC[A/T]GTTCAATTCCTCCTC	23077
rs547808485	snp	G/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77272722	GTCTTGTTTGACCAG[G/T]AGAGTTCAAAATCAC	23077
rs547809584	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77250431	TGGGCTTCTCTTCAC[A/G]AAATTTTCTCTACTC	23077
rs547820363	snp	A/G	1.73724e-05	0.00294719	intron-variant	MYCBP2	GRCh38.p7	13:77206624	CACACATTAATGTGA[A/G]TTAATGGTACATCAA	23077
rs547831208	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77198435	GTGTTAACATATTGA[A/T]ATCATTTTTAGATAT	23077
rs547835625	snp	A/G	5.04494e-05	0.00502217	intron-variant	MYCBP2	GRCh38.p7	13:77057139	AAATATAATAATGAT[A/G]AACAGTTGAGTGACT	23077
rs547842728	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77238079	AAACCCCATCTCTAG[C/T]AAAAATACAAAAAAT	23077
rs547845935	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77320607	CAAATTTTTACCCTG[C/T]GATTACTTGTTCTTT	23077
rs547853862	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77281710	CAAAGAAAAATGATA[C/T]ATAAAGAGTCTTTCA	23077
rs547861318	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77298269	CTCCTGCTAACCACT[A/G]CTTATCTTCGAGGTC	23077
rs547884527	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77167622	TTACATGATGTTTGC[A/G]GACATTAAATTGTTT	23077
rs547891211	snp	C/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77214387	AACCACGTAAATATA[C/T]AAACATGAGAAACTG	23077
rs547900057	snp	C/G			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77080907	GATTGTGCCACTGCA[C/G]TCCAGCCTGGGTGAC	23077
rs547909714	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77106014	TGATAATAATAAAAC[A/C]GTGTAACTTTTCTTT	23077
rs547944186	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77138156	AAAGCAGTAAGCCAA[C/T]ACTCTAAATCTTCTT	23077
rs547950063	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77101965	ATTCATCTCCTAATT[A/T]ATTTAATGACTGTAC	23077
rs547951282	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77307274	TGAGATTTTGCTCAA[A/C]CATACATCCCTCTCT	23077
rs547953192	snp	C/T	1.72892e-05	0.00294012	intron-variant	MYCBP2	GRCh38.p7	13:77262153	CGAGACTAATAAATA[C/T]TATTGCATTTCTAAT	23077
rs547994242	snp	C/T	1.66032e-05	0.0028812	missense	MYCBP2	GRCh38.p7	13:77190318	GATTTCTTTGAACTC[C/T]TGAACTGGAAAACAA	23077
rs547998622	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77321517	GTGATCAGTGTCTAC[C/T]GAATAAAATCTAATT	23077
rs548011248	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77314560	TATAGCACATTCTGG[A/G]AAAGGCAAAACTATG	23077
rs548024599	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77128193	TCTAAACTTTACATA[A/G]TACTTGCTATTACAC	23077
rs548037669	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77131669	TTCATATAGTATAAT[C/T]TCACAGATTATTATA	23077
rs548037885	snp	A/C	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77146717	GGAAAATACGAATTA[A/C]AACAAAACTAAAATA	23077
rs548050772	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77207965	CCACCAAGCCCCACC[C/G]GCCCCAGCCCCAGAT	23077
rs548055455	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77199643	ACTTAAATGTCCCTG[A/T]CTGACAGCTTTGAAG	23077
rs548062153	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77122321	TTCCATTAAAATAAC[A/C]TTATGAAAAATAAAA	23077
rs548063652	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77072914	GTACTAGTTAGATTA[A/T]ATATGAGTCTCTTTT	23077
rs548068811	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77247033	GAGAGACTGAAAGCT[C/T]TTCCTCGTAATATCA	23077
rs548084357	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77244940	CACCCCATCAAAAAG[C/T]GGGCGAAGGATAAGA	23077
rs548088231	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77130032	CTAGAAAAATTAACA[A/T]CTTCACAAAATGTTT	23077
rs548121856	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77121225	CTATGAAAAGAACAC[C/T]TTTGTAAACATTTTT	23077
rs548134812	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77080463	TGGCAGTTAGTGCTA[C/T]TTCTTTCTTGGTTGT	23077
rs548135428	in-del	-/A	0.208169	0.246476	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77292959	GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	23077
rs548145743	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77167792	TAACAGTTGAAACTG[C/T]TGAATCTGGGATGAT	23077
rs548155838	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77171116	TTTAGACAAGTGCCT[C/T]TGAGGAGATGGTTAG	23077
rs548165935	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77261761	CAAAGTGAGCACAGG[C/T]GGTTAGAAAAATGAT	23077
rs548176010	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77121644	TTAAATACCAGTCAG[G/T]TCATCTTAACATTAA	23077
rs548194803	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77113531	AGATGGTAATGAAGG[A/G]TGAAATAAACACAGT	23077
rs548202194	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77105784	ATATTAAAAACAATT[G/T]TAAAGAATCAGGATT	23077
rs548205900	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77276601	TTTGAAACTTTAAAC[A/G]AGAAAATAAAAATGA	23077
rs548211161	snp	C/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77153535	AAGCAACTATATTTA[C/T]CCTAAGTATTTAATA	23077
rs548212329	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77197841	TAGCCCACTCACTGG[A/G]TAATTGAATACAAAA	23077
rs548212420	in-del	-/C			intron-variant	MYCBP2	GRCh38.p7	13:77294806	CAGATTATTTTTCTG[-/C]CTACCCGGCAACACT	23077
rs548219890	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77166626	CATCTGCATCTGTAT[C/G]TGTGTGTGTGTCTAT	23077
rs548240431	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77298751	AGGTCATGGAAACTA[C/T]GTATGTGGATGAGAT	23077
rs548258059	snp	A/C	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77144090	CAGGCACTGAGCTAC[A/C]CTGGAAGATCCAAAC	23077
rs548261083	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77049770	CCTCGTGAGTAGCTC[A/G]GATTACAGGTACCCG	23077
rs548284944	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77066641	GTTTTAGAAGTAGAA[C/T]TGGTAGGTCAAAAGA	23077
rs548290893	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77216976	CATACACACACACTG[C/T]GTGTGTGAGAAAGAG	23077
rs548294824	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77214419	ATGAATAAACTATCA[C/T]ATATACACACAATGG	23077
rs548324171	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77269396	ATCCCAGCACTCTGG[A/G]AGGCCCAGGCGGGTG	23077
rs548339623	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291743	TTGCACTCTAACCTG[C/T]GGAACAAGAGCGAAA	23077
rs548350158	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77128360	ATAAAAAAGCAAATA[A/T]CCATAGATTTAGCAA	23077
rs548351742	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081359	GTTGCTAAATTCAGA[A/G]ATGAAAGTGCATGAA	23077
rs548352419	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77145270	GCAATCTCTCAGTAG[A/C]ATCTGATAGCTGACA	23077
rs548354018	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77241460	TATTTCTAAAGAAAG[A/T]AGAAACAGGTAGCAA	23077
rs548355992	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77183065	ATGGTAAATTACATC[A/G]ATTTTCAATTATTTA	23077
rs548358832	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77283697	AGCTCAAGAGTTCGA[C/G]ACCAGCCTGGGCAAT	23077
rs548388141	snp	A/T	4.95168e-05	0.00497553	missense	MYCBP2	GRCh38.p7	13:77097718	TCATTGTGTTATGCA[A/T]GGACATTTCAAAAGT	23077
rs548391652	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77191420	TTCTAATTTGGTAAT[C/G]AAGCTCGTAAACAAT	23077
rs548406330	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77282972	ACTCTCTAGACAACT[G/T]CAATAACTGCCTAAA	23077
rs548411457	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77131198	GCAGAAATTTGACTA[A/C]CAGAAAGCTGGAGTT	23077
rs548427125	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77050575	TTGACTTTCTGATGC[C/T]CACTACACTACTGAT	23077
rs548440345	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77144688	CACCCTGCCATAGTA[C/T]GCTTGCCTACTCTCC	23077
rs548468656	snp	A/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77247159	AAGCAGAAAGGAAGA[A/T]GTAAAATTATCTATG	23077
rs548483370	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77073522	TCTATTCAGCATGGC[A/G]CTTAAGGGCTTAATC	23077
rs548489830	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77178067	TAAGTGGATATAAAC[A/G]TTCCTAAAGGTATGT	23077
rs548501993	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77321086	GAATTTTATTGTATA[C/T]AAATTAAACCTCAAT	23077
rs548505435	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77130468	GTACACACCCATCTA[C/T]ATAAATATATACTAA	23077
rs548506126	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77174565	ACTCTAGCAGTAAAA[C/T]AGGCAAATATACTGA	23077
rs548518289	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77147510	CTGCTCATCTACTTC[G/T]AACTCCTCCTGTACT	23077
rs548523537	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77312422	CCAAGTATAGTATGC[A/G]TGACAACTATAACAT	23077
rs548524028	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77065511	GAGCAACTAATCAGA[A/G]CCAGGCATTCTGTAA	23077
rs548563651	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77222862	TTTAATGACTATGTG[A/C]AGGTAAGTTCTCTTT	23077
rs548563927	snp	A/G	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77166868	TGACTCTCTAAGTGT[A/G]TATCCAATGAATGCA	23077
rs548566750	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77208154	TTTTCCTTTTCTCCT[C/T]CTGCTCTCTTTTCCT	23077
rs548568247	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77135965	CTCAGCCTCCTGAGT[A/G]GCTGGGACTATAGGC	23077
rs548584221	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77117140	ACAAAATTAATAAAC[G/T]AACTCCTCACTTCTG	23077
rs548601249	snp	A/G	1.64825e-05	0.00287071	missense	MYCBP2	GRCh38.p7	13:77168433	CGGTGCCTACCTTGT[A/G]ATGCATCACACAGGC	23077
rs548612693	in-del	-/TC			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77085545	AAAACAGCCACAAAT[-/TC]TCTGTCGCTCTTTCC	23077
rs548616840	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77184219	GAAACATTTTAAAAT[C/T]TCCTTTATAACTTCT	23077
rs548620324	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77157459	CAACTCCTATGCTCT[A/G]GCAATCCACTTACCT	23077
rs548638233	snp	A/G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77321831	GAATTTGTGTCTTAT[A/G/T]AATTTTTATAGGGCC	23077
rs548639396	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77239341	AACAGGCCAAAGAAA[C/T]AAAAGATCTGTATGT	23077
rs548640649	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77060907	GATCCTCTCACTTTA[G/T]AAATGAAGTCAATGA	23077
rs548646689	in-del	-/A	0.327445	0.237702	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77227344	AAGAATGGATGGACT[-/A]AAAAAAAAAAAAAAA	23077
rs548647402	snp	G/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77139834	TCGAACATTGTTCTT[G/T]TCATGTTCAAAATAT	23077
rs548657619	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77107311	GAAACTAGTTTATTG[A/G]TTCTTATAGACAATA	23077
rs548676731	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77171209	AAGCTTTTTGATTAC[C/T]AAAAGAAGAATAAAG	23077
rs548677222	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77208976	CAAAGTAAGCTAATA[C/T]TGGATGTGCAATGCA	23077
rs548677500	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77266065	AATAAAGACATTAAC[A/G]AGTAATTTTTTTATC	23077
rs548683448	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77156794	TGATCTACACATTCA[A/G]GTTGTCCTGTGAGCT	23077
rs548698288	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77161371	TAGTTAATGCCTAAA[C/T]GAGCAAAAAAGGTAA	23077
rs548724882	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77314633	GGAATAGGTGGAGCA[C/T]AGATGATATTGAGGG	23077
rs548733361	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77058132	GGCATGAGCCACTGC[A/G]CCCGGCCTCAATCAA	23077
rs548734431	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77280131	AACCAGAAGCAAGTC[A/G]GCTGAAGGTAAGTCA	23077
rs548750619	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77295418	ATTACAGGCGTGAGC[A/C]ACTGCACCCAGCCAA	23077
rs548755601	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77200023	GTTCCTCACCAGCAA[C/T]GGAACAAAGCTGGAT	23077
rs548769769	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77091585	GGTTAGCAACATCCC[C/T]GGCCTCAACTCACTA	23077
rs548771758	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77054141	ATGACAGCATGTGTG[C/T]ATGGGGTTGGGGGTG	23077
rs548773448	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77195083	AGGTGAATTGCAAGA[A/G]AGGCAGATAAAGATT	23077
rs548813776	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77308176	ACTTCAAAATCCCTC[A/C]CCTACCCATCAACTC	23077
rs548814418	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77223241	AAGGTATGAATGTTG[A/G]TCTATTCCTGCCCAA	23077
rs548835553	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77296211	GATTGCTTGAGCCCA[C/T]GAGTTCGAGACAAGC	23077
rs548842267	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77199706	ATCTGAGAAAGGGCA[C/G]ACTGCCTCCTCAAGT	23077
rs548882043	in-del	-/A	0.00557542	0.0525036	intron-variant	MYCBP2	GRCh38.p7	13:77108256	GAAGAAAACATACTC[-/A]ATAGCATATTATTGA	23077
rs548889853	snp	A/C	0.00478085	0.0486577	intron-variant	MYCBP2	GRCh38.p7	13:77303600	GTTTGGCAATCAAAA[A/C]AACAAGACTTCTAAA	23077
rs548893275	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77151306	ATCAGGTAATGCAAG[C/T]GTAAATGCTTTCCCA	23077
rs548901896	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77247925	TAAATGTAAGACCTA[A/G]AACTATTACAAAAAA	23077
rs548906733	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77092051	TAATCCACACAGTTG[A/G]GGAGGGGAGAAGTTG	23077
rs548924102	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77109644	TCTTTCTCACTTCTT[C/G]CAGTCTATGTAAGAT	23077
rs548941374	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77102580	AAAACATATTTTTAA[A/G]TTGTCTGAAATTTTG	23077
rs548951237	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77311401	GTGAACAACTTCAAG[A/G]GAAGAGACAATCAAA	23077
rs548963047	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77163699	TACCTATATTCAAAT[A/G]GACCGCCCTTCCTTA	23077
rs548968041	snp	A/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77210804	TCTCAACAGTAAAAT[A/T]AATAATTATAATGAT	23077
rs548970053	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77143870	TGGTAAGGATTTGCA[C/T]ATCTAAACATATCTA	23077
rs548993992	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77046297	ACGCTAGGCTTATAC[C/T]TGAAAGCAGAGTCCC	23077
rs549007663	snp	G/T	1.64765e-05	0.00287019	synonymous-codon, utr-variant-5-prime	MYCBP2	GRCh38.p7	13:77288254	AGATGCGGCTGCCAA[G/T]GATATTTCCTTTTTC	23077
rs549035817	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326228	CTCACTATCCCCCCA[C/T]ATAGGCAGGCAGACA	23077
rs549048418	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228384	TGGTGGTGAATACCT[A/G]CAGTCCCAGCTACTT	23077
rs549054903	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77066764	ATGTTGCCAAAGCAT[C/G]AAAGATATTTTGCAA	23077
rs549066711	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77181250	TGATTTATGTGAATG[C/T]TTCCTATACCTATTA	23077
rs549066980	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77172233	TTTAAAGACCCACGC[A/G]AAGAGCTGAGGGAAA	23077
rs549073042	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77327103	GGAAGCTGCCGGCCT[C/G]ACAGAGCATGCGCCA	23077
rs549129732	snp	G/T	1.66624e-05	0.00288633	intron-variant	MYCBP2	GRCh38.p7	13:77061817	CATTTCCACGTTACT[G/T]AGATTAACAAGCAAG	23077
rs549130188	snp	A/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77213147	CTCTTTTAAGATCTG[A/T]CCTTATTTTTTGACA	23077
rs549134776	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77188408	ACTTAGGTAACATAC[C/G]TAAGAATCCTCAATT	23077
rs549137535	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77159484	ATTATAAACCATATA[C/T]GAACTCTGATATGGT	23077
rs549154369	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77203978	TACCATTCAGGACAT[A/G]GGCATGGGCAAGGAC	23077
rs549160755	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77055003	CTAAATCTCAAAAAT[G/T]TTGGGGGGTCATAAA	23077
rs549198381	snp	A/C/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228928	TGGAGGGTAATCCTA[A/C/T]AGTCATGCATATAAC	23077
rs549204445	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77327709	AACGGAGCAATAATA[A/T]TTTTTAAATTACTCT	23077
rs549204804	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77221506	GATAACATAACCTGA[C/G]TATAACATGGCCATG	23077
rs549211140	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77243002	ACTTTTCAGTGGTTT[A/C]AGGATAGGGTAGGAA	23077
rs549225450	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77135529	TAGTCCCTACAGAAA[A/T]TCATACCTGTCCCTG	23077
rs549228229	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77140501	CATTTTTTTAACATG[C/T]AGTTTACCAAAATGC	23077
rs549231033	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77070986	TTTGATTAAATCTAT[G/T]TCTAAATTGTAAACA	23077
rs549242147	snp	G/T	0.00478085	0.0486577	intron-variant	MYCBP2	GRCh38.p7	13:77202598	CACAACCAAAAAAGA[G/T]AATTTTAGACCAATA	23077
rs549260747	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77243438	GCCAACATGGTGAAA[C/G]CCCGTCTCTACTAAA	23077
rs549265444	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77111621	TAGAGACAGGGTCTC[A/G]CTTTGTTGTCCAGAC	23077
rs549272474	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77187923	TAAAAATACAAAAAT[C/T]AGCTGGGCGTGGTGG	23077
rs549288553	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77143261	TTCCAGACAAGACTG[A/G]CGTGTGAGTGTGAGT	23077
rs549309795	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77095128	TTTCTAAGACATGTT[A/G]TGTATTAATACAATG	23077
rs549315192	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77281136	CTTATAGTCAATGAA[A/C]ACACATATTTCTCCC	23077
rs549315805	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77280159	TCAATTGTAGTTCTG[A/G]TTAACATTTACAAGT	23077
rs549334571	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77110775	ATAGAAAGAACCTAC[A/G]TTGAAATATTGGGGG	23077
rs549341063	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77274954	TACCTTTTCCTCCAG[C/T]TATCCTTCCTTCCCT	23077
rs549354641	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77233130	TGGGAAAGTATCCCA[C/T]CTAGGTGATAAGGAA	23077
rs549355772	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77286735	CACTCCAGCCTGGGC[A/G]ACAGAGCTAGACTCC	23077
rs549382968	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77305450	AACAAAAGGTCATAA[A/G]TTGTATAATTCCATT	23077
rs549399308	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77118993	TTATTAACATAGCAA[C/T]GTGTTTACATTATAG	23077
rs549403032	snp	A/T	0.00517822	0.0506191	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77077762	TGGAAACCTCACAAG[A/T]TCAGAAAAGGGTTCT	23077
rs549444319	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77273760	TTGTCTCATTATAAA[C/T]GAAATTTAAGGAATC	23077
rs549447315	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77158964	TATCTGACAAGCAAG[C/T]CTTATGTTTTTGGAG	23077
rs549447888	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77219819	TACCGAGAGCAGGAG[C/T]TTTCAACTCAGATAT	23077
rs549452634	in-del	-/A/AA	0.516115	0.0851984	intron-variant	MYCBP2	GRCh38.p7	13:77261386	ATATCTTATGTATTA[-/A/AA]AAAAAAAAAAGGAAT	23077
rs549471203	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77258962	ACCCAATTAAAAGCG[C/T]TGGTGCCAAGGGCCA	23077
rs549472612	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77274368	GATTCAATCAACAGA[A/C]ATCTGGGTATTTCTT	23077
rs549480063	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77129029	AACTCAATTGCAGCA[C/T]TTCATATAGATCTTT	23077
rs549485730	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77212390	AAGTGCATTATTTTT[A/T]AAAAAAAAGTTTGAA	23077
rs549500104	snp	C/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77267085	CTATGAAATTATTGA[C/T]AGACACATTAGACAC	23077
rs549501352	snp	A/G			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076968	TTGCTAATATACACC[A/G]CTATTTTTCTTAATT	23077
rs549522827	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77219475	TTTTTTTTTTTTAAT[A/G]ATAAGAGATTTGAGG	23077
rs549523422	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77304408	GCATGTTTTTACTCA[C/T]ATGTGGAAGCTAAAA	23077
rs549533623	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77237371	TCTCTGTACATGATT[A/G]TATTTTAATAGAGTA	23077
rs549537220	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77274111	TTAATATAAAATTGG[C/T]TATATCATTAACATA	23077
rs549546571	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77238794	ACAGTAACTAAATTA[A/C]GTCAATAGGCCTGAA	23077
rs549551415	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77318733	CACTCTGGCCTGGGT[G/T]ACAGAGCGAGACTCT	23077
rs549554304	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77311707	CCTGAACGTGTATCA[A/G]TAAAAATAACCTCAT	23077
rs549574697	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77110944	CATCATAAGACATAA[C/T]GGCTGCTGCTGATGC	23077
rs549581333	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77210945	ACAGAAAGCAAGTTG[A/T]GGAGCTGGGATAAAC	23077
rs549594209	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77242176	TGGAGTGCAGTGGTG[C/T]GATCATGGCTCACTG	23077
rs549613633	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77304590	CAACTTCAAACAGCT[A/G]GAAGAGAGGATTTTG	23077
rs549613796	in-del	-/A	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77105695	CCTGTTAATACAGAT[-/A]AGACAACCAGTTATT	23077
rs549617685	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77252405	TTATGAAGCTTATAA[A/T]GTAGTAAGAAAGACA	23077
rs549627172	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77299862	AAGGCTATTAACATG[A/C]CTTAAATATTTATCT	23077
rs549628092	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77213616	TACTACCAACTAATA[C/T]GAAGAAAAGCAGTCC	23077
rs549646855	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77137135	TTACCGCTCCTCTAA[C/T]CTTTGTTACTCCCTT	23077
rs549664090	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77260666	GTTTGTATATAAAGC[A/T]AAAAAAAAAACCCAT	23077
rs549670834	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77311698	GTCTGTGAACCTGAA[C/T]GTGTATCAATAAAAA	23077
rs549701200	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77259939	TCAAACTTTTGGTTT[A/G]TCAGTCACCCAGGCA	23077
rs549714315	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77136277	CATGGCAATGTAATA[C/G]AGTATCTCATTTGTT	23077
rs549714365	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77144305	AAATACTCATTATGA[A/G]AGAGAAAACAAGGCC	23077
rs549718012	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77102661	TCACTAGGAAAACAA[C/T]ATTAGAAAAATTTAT	23077
rs549744459	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77157563	CCAGCCTGGGCAACA[C/T]GGGGAAACTCTGTTT	23077
rs549747269	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77062756	GACTTATGAAATGCT[A/G]ACTGTGACACATCAC	23077
rs549748460	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77062883	CCTATGTGCCATGCA[C/T]ACAGGAGGCACTCAG	23077
rs549761886	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77047267	AGGCAGAAACGATTA[C/T]CCTCATTTTGTAGAT	23077
rs549762467	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77237418	ACATTTACTTTGAGG[A/G]GGGGATGGAAATGGG	23077
rs549767481	in-del	-/TG	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77108014	ATTTGTTTATATAAC[-/TG]TATTTATGTAAGACT	23077
rs549775036	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77266175	CAGGGTTTCTCAGAA[A/G]TAAATCCTTGATATT	23077
rs549775853	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77202754	TATATGCAAATCAAT[A/C]AATGTAATCCAGCAT	23077
rs549800236	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77054358	GGGAGACTGGGCTAC[C/T]GTATTATAAGTAGAA	23077
rs549800950	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77282012	ATATTTGGTACAGAG[A/G]TAATATCTACAAATA	23077
rs549810263	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77057486	AATATAAGCAATGGG[A/C]AAAAGTTAAAAAAAC	23077
rs549823795	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77189256	TTAAATCCTACCTTC[A/G]CAAGACCGAGTAGTA	23077
rs549840466	in-del	-/A	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77057214	AAAATCAAGAAATTT[-/A]CTATAATGAAAATTC	23077
rs549843022	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77310738	AAACTGAAAGGATAC[C/G]AAGCAGGATACACAC	23077
rs549878287	snp	A/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77275678	TAAATAAATAAAAAA[A/T]TTTTAAGTTAAAAAA	23077
rs549887912	snp	A/C/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77204912	GTGGGGTGGGGGGAG[A/C/G]GGGGAGGGATAGCAT	23077
rs549918323	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77095757	AACATTCATTTCATA[A/T]TCATCCTGGGCTGAC	23077
rs549927739	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77129096	TTTTAAAGACACAAA[A/G]TTTGTTATACATGCT	23077
rs549928246	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77243518	CTCGGGAGGCCGAGA[C/T]GGGACAATCACTTGA	23077
rs549937008	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77054867	TGGCCTCCCAAAGTG[C/T]TGGGATTACAGGTGT	23077
rs549939721	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77314003	AGAACATAGACAACA[C/T]CAAATGTTGGCGAGG	23077
rs549939763	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77305978	TCCACTTAGGCATAG[A/G]AGGAAAATGCAAGGA	23077
rs549945481	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77053182	TCTGTTCAGAATTCT[C/G]CTCATAGTTATAAAG	23077
rs549948930	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77296360	AGGAAACTACTGGAC[A/T]CCAGCCTGGGTGACA	23077
rs549958564	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77320384	AGAATTAAGCATTTA[C/T]GCTGCTGGATTAGGA	23077
rs549959268	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77152022	AATTCAACAGAATTG[A/T]CACAGAAATAGAAAA	23077
rs550091900	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77094417	ACATTAGCTTCCACA[C/T]TCCACAGTGATTTTT	23077
rs550101006	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77275088	TACCGAACTCTCACA[C/T]ACTGGCAACTATTCT	23077
rs550107873	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77088142	TGAAACAGTTAATAA[C/T]TTGGGGTTTTAATTT	23077
rs550142102	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77182219	ACAGTACTCTCTAGC[A/G]CTGTTTCAAAGGGAG	23077
rs550143201	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77187569	GATTGAATAAATTAG[A/G]ATAATGGTACGCAAA	23077
rs550143615	snp	A/C			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77078265	CAAGCAAGCGATTGG[A/C]CAACTTTTTGTGAGA	23077
rs550162659	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77237966	TAATAGCAACATGCC[A/G]GACGCGGTGGCTCAC	23077
rs550178970	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77327867	AATTGTGACGGAGAC[C/T]GTATAGCGTCTGAAA	23077
rs550201013	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77285333	TGGTATTCTAACTAA[A/C]AAGTAAATTATACAA	23077
rs550209285	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77065060	CTATGTTTGAGAAGT[C/T]TGTCACTTAGCATAA	23077
rs550216059	snp	C/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77309995	TGGGTGCCTGTAGTC[C/T]CTGCTATGTAGAAGG	23077
rs550220454	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77229001	TTAAAACAAATCAGC[A/T]AGGACAAAAGTAGTT	23077
rs550241298	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77152765	AGAGCCACTTCCACC[A/G]TTTGATAAAATCCGC	23077
rs550245004	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77079555	TGATACAACTCAAAT[A/C]AACAAATGCTGTGTA	23077
rs550246111	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77121038	TTCTCATTAACATTA[C/T]CATCCTAATAAGTGG	23077
rs550250859	snp	C/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77274681	ATAACTCCACTTTTC[C/T]CTATCTCATCATCAT	23077
rs550264579	snp	G/T	3.71547e-05	0.00430998	intron-variant	MYCBP2	GRCh38.p7	13:77267961	AGCAAAAAATTTTCC[G/T]GTTAAAATATTTATT	23077
rs550265976	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77177619	GAGCCACTGTGGCCA[A/G]TCTTTTTCAATTTCT	23077
rs550272613	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77072536	ATACAAGGCAAACAT[A/G]GGGAAAGAAATAAAG	23077
rs550282518	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77169213	GGAGATCGAGACCAC[A/G]GTGAAACCCCGTCTC	23077
rs550295397	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77221418	CCCTCTCAGCGGCCA[A/G]CACACCTCAGTGTGG	23077
rs550326488	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77110283	TATAAACGGCTGCTC[C/T]GGGAGTGTCTGTCTT	23077
rs550334092	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77230019	ATGTTAATTCTGTTT[C/T]GAATATAGTTTATAG	23077
rs550334140	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77220784	GGTTGCTACTTTCCA[A/G]GTTCCACAAAAGTCC	23077
rs550363115	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77162030	CTAGTCCTTTGCATT[A/C]ATTACACTTTTTTTA	23077
rs550364757	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77105846	TTTGCTTACTATAGT[C/T]TGCCCTCATAAACAA	23077
rs550365500	snp	C/T	1.64912e-05	0.00287147	missense	MYCBP2	GRCh38.p7	13:77068647	TGAGCCAGATATTGC[C/T]GGCCAACGTTAGAGC	23077
rs550396141	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77319102	GTGCCTTGGTGCAGT[C/T]TGGGAACGTGTGTGT	23077
rs550398296	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77124984	GAAGTACTGAGATTG[A/G]TAGTTGGAATACCGA	23077
rs550402096	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77215985	AGTGCCCAGTTAGTG[A/T]CTAATACTATTCCCC	23077
rs550416512	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77271102	ATCATACTTTTGATA[A/T]TTTCTTTTATTACTT	23077
rs550421431	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77309973	AAAAATTAGCTGGGC[A/G]TGGTGGTGGGTGCCT	23077
rs550428315	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77156363	TGAGTGTCTCCCTCA[A/G]AAACTGTTAAGGACA	23077
rs550430254	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77112604	CTGATCTTTAAAAAA[A/T]TTTTTCTTAATTTTT	23077
rs550430556	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77274746	AAAAGTGTTAAGAAA[C/T]TATCTCTTACCATTC	23077
rs550431946	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77053069	TTTGAGCCCAGGAGG[C/T]GGAGGCTGCAGTAAG	23077
rs550439827	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77201154	AGGAAACCCATCTCA[C/T]GTGCAGAGACGCATA	23077
rs550454001	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77261649	CCTAAAATAATTACA[A/G]TAGTAACATCAAAGA	23077
rs550483462	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77317028	AATCTCGGCTCACTG[C/T]AACCTCCACATCCCA	23077
rs550485247	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77309445	AAAGAGGTTTTACCT[A/G]AAAACCACAGACCAG	23077
rs550498740	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77253359	TAATAACCAAAACTG[C/G]AAACCATCCAAATGC	23077
rs550500812	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77106582	GGATGCTACAAATGA[A/G]GACAGCAAAAAGAAT	23077
rs550501392	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77320807	TGAACACCTAATAAA[A/C]CCTTAAGGTCTAGCT	23077
rs550507480	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77124223	TTTAAATTCTAGAGC[C/T]TGAGTTTCCTACCTA	23077
rs550514212	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77195490	TAGTCCCAGCTACTC[A/G]GGAAGCTGAGGCAGA	23077
rs550532443	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77084927	GCCAACACAACTGAC[A/G]TACTCTGCTTGGGCT	23077
rs550532893	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77108500	AAAGTAAAAATCTTA[C/T]TCCCACAAGTTGCTT	23077
rs550538019	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075469	TCTGATCAGTCCTTG[C/T]TCCCATTCTCTCTAC	23077
rs550554216	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77230144	TATAGGATGAATTCT[A/G]ACCTTCTCTGAATTT	23077
rs550559200	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77150469	GTACTTTCACAGGAA[A/C]TGAAACTCAGCCTAA	23077
rs550560549	in-del	-/TATGTGTATGGATATATACACATACATA	0.00517822	0.0506191	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77083510	GTGTGCATATATATG[-/TATGTGTATGGATATATACACATACATA]TATGTAGGTATGTTT	23077
rs550565574	snp	C/T	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77249041	CTCTGATTCTCTTTA[C/T]ATGAGAGGTACCTAG	23077
rs550575770	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77156420	ACAGGAGATTTCTGA[A/T]ATTTAAATACAGTAT	23077
rs550579194	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77184827	CTCTCCCCTGGTCAC[C/T]ATGGTTCTTTTCCTC	23077
rs550584601	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77279604	GGAGAAGTAACAGAA[A/G]AATTGAAATAAGACT	23077
rs550602142	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77201882	CAGAATCTCTGGGAC[A/G]CATTCAAAGCAGTGT	23077
rs550602170	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77195114	AAAATGCATTAAAAT[G/T]TACTGGACAAGTACT	23077
rs550612399	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77235025	AAGCAATTGGGCTCG[A/C]AAATACTATTGTATC	23077
rs550612805	in-del	-/TA			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228056	TTAAAATATATATTT[-/TA]TATATATATCTGTAT	23077
rs550619817	snp	C/T	4.99929e-05	0.0049994	intron-variant	MYCBP2	GRCh38.p7	13:77233284	GAGAAACATTTTGTA[C/T]GTGCATAGAAAAACT	23077
rs550637124	snp	A/G	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77163368	TGGGAGAAAAGGGAT[A/G]GAGAAGAATAAAAGG	23077
rs550640221	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77083406	CAAGCAAAATCAGCA[C/T]GCAAATGAATAAATG	23077
rs550647819	snp	C/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77323848	AGTACTCACCTCCAC[C/T]CCTTCTATATTAACT	23077
rs550668288	snp	A/G	0.000348412	0.0131941	synonymous-codon, utr-variant-5-prime	MYCBP2	GRCh38.p7	13:77278845	GACTCCTGAGACACA[A/G]GGATGGATGAGAAAA	23077
rs550669258	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77085922	ACAGATAGCTGTTAC[A/G]GGTATATGACAATCT	23077
rs550671919	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77093614	TAAGCCCACCAACCA[A/T]CCAGTTGCTTAAGCT	23077
rs550674669	snp	G/T	3.47415e-05	0.00416768	intron-variant	MYCBP2	GRCh38.p7	13:77067888	AAAAATAAAATGAGA[G/T]AATTCCATGTAAAGA	23077
rs550689421	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77115382	AAATTAAAAAGTAAA[C/T]TGTAGAACAGTAAAG	23077
rs550701796	in-del	-/AAAC	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77240625	AATAAATAAATAAAT[-/AAAC]AAACAAACAAAACAT	23077
rs550731975	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77234177	TAGTTACAACTTAAA[A/G]TTTTAGGTTTTTTTC	23077
rs550738838	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77101990	CTGTACTTTTACATT[C/T]AAATGATAATATGCA	23077
rs550749528	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77162803	CTGGGACTACAGGCA[G/T]GTGCCACCATGCCCG	23077
rs550752070	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77108868	GCCACCACACCCAGC[C/T]AATTTTTTGTATTTT	23077
rs550753570	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77216999	AGAAAGAGAACAGCC[A/G]CATGTGCAATAATAA	23077
rs550771112	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77295354	GGCCAGGATGGTCTC[A/G]ACCTCTTGACCTCGT	23077
rs550775616	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77070102	AAATCAAATCTGATA[C/T]AGCTGGGTATTTGAC	23077
rs550789265	snp	A/G	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77046032	AAGTACCTGAAGGAT[A/G]TTAGCAGGAAAATGA	23077
rs550806014	snp	C/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77202268	CTACAAAATCCTCTA[C/T]GCAAATAAACTAGAA	23077
rs550810321	snp	C/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076902	GGCATTAACACTATA[C/T]TGGCCAGAGGACTCA	23077
rs550825797	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77231444	TAGAGATGAGGTTTC[A/G]CCATGTTAGCCAGGC	23077
rs550829497	snp	C/G	0.00557542	0.0525036	intron-variant	MYCBP2	GRCh38.p7	13:77168797	AGAAATCTTTCAATT[C/G]ATTAAAAAAAGATTT	23077
rs550857413	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77118068	GCTTTATCCTTTTGG[C/G]ACATCTTGAAGTAAG	23077
rs550857962	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77257453	CCCATTTACCCTGTG[A/C]TTATTATTACACATT	23077
rs550885706	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77179778	CACTATGTGTGCACT[A/G]TGAGTAGGGCCTGAC	23077
rs550888583	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77109265	CAAGATGGAACTGCT[C/T]CACCTCAGATCATCA	23077
rs550898499	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77226536	ACTAGTCTAAACCAC[C/T]CTCAAGTGGTATAGC	23077
rs550899083	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77264720	ATGCACAAGCTCAAT[C/T]GTAACAAGGGATACC	23077
rs550904561	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77080658	GTAGACACTTGAAGA[C/T]AGGCTGGGTGCAGTG	23077
rs550911961	snp	C/T	0.000201562	0.010037	missense	MYCBP2	GRCh38.p7	13:77164457	GGCCACACTTACCAA[C/T]AGGAAGTGCTAGGTC	23077
rs550914364	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77135188	TTTCACTTCTTTTTA[A/G]GTTAGCAGCATTGGT	23077
rs550940651	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77235829	AAGGTAGACAGTGTA[C/G]AGATAAAAGAAACCA	23077
rs550946830	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, utr-variant-5-prime	MYCBP2, LOC107984564	GRCh38.p7	13:77327044	CGCCACTGCCGCCGC[C/T]ACCACCGCTACCACC	23077
rs550961720	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77279550	CAGGCAATGTCAACA[A/T]TCTGAGAACCAGTTC	23077
rs550988379	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77191426	TTTGGTAATCAAGCT[C/T]GTAAACAATGTAATA	23077
rs550996530	snp	C/T	5.89547e-05	0.00542899	intron-variant	MYCBP2	GRCh38.p7	13:77278932	TAAAAGGAAAAAATA[C/T]ATATACTTTATGACA	23077
rs551000997	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77141856	ATTATTATTATAACT[A/G]TTCTAGTGAATTATT	23077
rs551026917	snp	A/C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77052498	GCCACATGCCTGGCC[A/C/T]AAAGCTATTTCGACT	23077
rs551036042	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77134670	GATCTGAACCCTTCA[A/T]CTATTTAGCTCTATC	23077
rs551049190	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77125573	GTGTAATCATTCCAA[A/T]ACATTTCTACTAAGA	23077
rs551052219	in-del	-/AGGATAGCAGGTTT	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77196711	ATGGGGAAGAACATG[-/AGGATAGCAGGTTT]AGGCAGATCATCAGA	23077
rs551064800	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77238910	CTGATCACCTGAGGT[C/G]AGAAGTTTGAGACCA	23077
rs551070702	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77287039	ACAGGCGCCCGCCAC[C/T]GTGACGGGCTAAGTT	23077
rs551073889	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77218778	CATTTTTAGTAACCA[C/T]TATCTGTAATTAGAA	23077
rs551076909	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77143016	TTTCCTTGAGGAGCA[C/T]CAGGAAAAATAATGT	23077
rs551078053	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77162910	TCCACCCACCTTGGC[C/T]TCACAAAGTGCTGGG	23077
rs551085622	snp	A/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77178488	ATTGAATACTACGAA[A/T]ATATACAGTGATATT	23077
rs551095334	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77242035	TACAAAAAAAAAATT[G/T]ACTGAGCAAGGAAAT	23077
rs551116582	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77324014	TCTCTCCATTTAGCC[G/T]CCCATATTTGCATAT	23077
rs551123118	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77046204	TATATTAATGTGCTT[C/T]ACGTCATGGGTTTCA	23077
rs551128143	in-del	-/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77070422	TTTTTTTTCTTGCAA[-/T]TTTTTTTTTAGTTCA	23077
rs551139555	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77302266	ACAGCATGGTCATAT[G/T]GCTAAAAGCAAAGCA	23077
rs551147851	in-del	-/CCTTTGTTTTTC	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77117043	GATCCTGATATTTTT[-/CCTTTGTTTTTC]CCTTTGTCCTTACCT	23077
rs551148148	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77280190	TTTCTGGAAACAACA[A/G]ATATAGCTAAGAAGT	23077
rs551153111	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77060858	GGGAATTATCAATAG[A/G]AATGTATTTTATCTA	23077
rs551153285	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77221186	ATATTTTGTTTCAAC[A/G]TTAAATGCTATCGTA	23077
rs551179121	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77170845	CTCCCAAAGTGCTGG[A/G]ATTACAGGCATGAGC	23077
rs551185918	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77116945	TTTGTCTGCTACTGC[C/T]ATGACACAGGCAATT	23077
rs551186287	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77178895	GACTTTCCTGCATCC[C/T]GCAGAGTATACTATC	23077
rs551188044	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77248915	GTAATATACATACAA[C/T]AGAATATTATTCAGC	23077
rs551204642	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77170689	TCAAGCGATTCTCCT[A/G]CCTCAGCCTTCTGAG	23077
rs551205355	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77310074	CCAAGATCGCCCCAC[C/T]GCACTCCAGCCTGGC	23077
rs551229751	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77303127	ATCATGAGGTCAGGT[A/G]TTCGAGACCAGCCTC	23077
rs551231087	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77317010	GCTGGAGTGCAGTGG[C/T]GCAATCTCGGCTCAC	23077
rs551234469	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77279689	TATTCTCTCTGCTGA[C/T]ATTTTTGCATTAATT	23077
rs551236387	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77266663	TGTGGGGGGAGTGTG[A/C]ATGTTATTAAAAGTA	23077
rs551236399	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77287479	TGTGAGAGCCACTGC[A/G]CCCGGCCTACAATAC	23077
rs551248604	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77195590	CTACCAAAGAGACTC[C/T]TAAAAAAAAATAGTC	23077
rs551248703	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77318032	TTATTCTGAAATGAT[C/T]CCTGTAGTAGAGGAT	23077
rs551256040	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77218947	GAGTGAAAGAGATGG[C/T]GACTTTGATAGCTAT	23077
rs551257498	snp	A/G	1.67055e-05	0.00289006	missense	MYCBP2	GRCh38.p7	13:77211188	ATTACATCATATACA[A/G]GATCAAGACACACAC	23077
rs551271960	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77265924	GACAAATATGGGACT[A/G]TCTTCCTGAAGTTTG	23077
rs551273378	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77262841	CTTTAAAAATTTTAA[A/G]TCTGTAATTTCAATT	23077
rs551274228	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326386	GCAGGTACACACACG[C/G]AAGCACACACACACG	23077
rs551305482	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77096787	TAGACAATACAAGTA[C/T]AAAAGTTCTATAACA	23077
rs551310252	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291623	AAATACAAAATTAGC[C/T]GGGCGTGGCGGTGCA	23077
rs551323817	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77187872	CGAGGTCAGGGGTTC[A/G]AGACCACCACCAACA	23077
rs551327497	in-del	-/AG	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77073306	TCTTGTCTGGGTGAC[-/AG]AGTTAAGACCAGGTC	23077
rs551367991	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77202449	GATGGATTCACAGCC[A/G]AATTCTACCAGAGAT	23077
rs551380886	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77125073	GAGGTATATAAATTT[A/C]TATTAATGAAATTAA	23077
rs551411464	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77317161	CTCACCATGTTGGCT[A/G]AGCTGGTTTCGAACT	23077
rs551411960	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77078585	AGGGTAGGGAGACTG[C/T]AGGTACAATATAATT	23077
rs551416249	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77224760	ACACACTTAAAAATT[C/T]GTATAAATGCCATTT	23077
rs551417860	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77070077	GGGGGAAAAGAAATA[C/T]GGGAAATGCAAATCA	23077
rs551429775	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77265000	CAACAAAACATAAAA[G/T]TCTGATTTTGAAATG	23077
rs551438258	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77286513	AATCCCAGCACGTTG[A/G]GAGGCCGAGGCAGGC	23077
rs551468480	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77325273	TTGCCTAATAAATTG[A/C]ACATTCAATAAATAA	23077
rs551477972	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77077675	CTACGATATGGCTTC[C/T]GAGCAAAATTATATG	23077
rs551479802	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77188350	CCAAAAACATCTTAC[A/G]CCCCTTATCTCATTA	23077
rs551491054	snp	A/G			synonymous-codon	MYCBP2	GRCh38.p7	13:77166341	TACCTGGCAACACCA[A/G]AACCATAGTAGGCCA	23077
rs551497803	snp	C/T	0.000151208	0.00869375	intron-variant	MYCBP2	GRCh38.p7	13:77217984	AAAAAAAAAGTAAGT[C/T]AATTTCTTACAAAAC	23077
rs551523254	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77094462	TTCATGTATTTCTCT[G/T]TTTAAAATTCTTCCA	23077
rs551527843	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77202014	CAAACACATTCAAAA[C/G]CTAGCAGAAGGCAAG	23077
rs551528443	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77069407	GCGGGCGGATCATGA[C/G]ATCAGGAGATCGAGA	23077
rs551536195	snp	A/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77257535	ACCCATAAAATTTTT[A/T]AAAAAAATTTAAATA	23077
rs551543216	snp	C/T	0.00636936	0.0560724	intron-variant	MYCBP2	GRCh38.p7	13:77069519	CCGAGGCAGGTGGAT[C/T]ATGAGGTCAGGAGAT	23077
rs551548017	snp	C/T	8.57655e-05	0.00654793	intron-variant	MYCBP2	GRCh38.p7	13:77070753	AAAAGAATGAAGTGG[C/T]CTCTTTAAATAAAAT	23077
rs551568523	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77101614	TGGTGAATATTTTCT[G/T]AAGATCTGTAAGTGG	23077
rs551586860	snp	C/T	0.00199481	0.0315187	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77327068	TACCACCGCCACCAC[C/T]GCCGGGGCTACCCGC	23077
rs551622008	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77164013	TTATCTACTTGCTGT[A/C]GAATATCTTTCATAC	23077
rs551628657	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77109451	CCTAACAGGCCTTGG[A/G]CCAGTATTGGTCTGT	23077
rs551653342	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77220571	ATTAATGTGTGCTAT[A/G]TAGTAAATTCCAGTT	23077
rs551653613	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77212409	AAAAAGTTTGAAATA[G/T]TTTCCACGCAAGAAG	23077
rs551662148	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77104947	ATAAACCTCAAAAGA[C/T]GTCAGGTGCTGCAAA	23077
rs551676944	snp	G/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77277395	TATTTGGTAATAGCT[G/T]TTAATAACTGTGTAT	23077
rs551689824	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77219674	GAAGTAGGTTTGCAG[C/G]GTTGGTGGGCTGAAT	23077
rs551701265	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228028	TTAATCTTTATCAGC[A/G]GCAGTGGCAGAATTA	23077
rs551714758	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77191568	AGCAGTTATATTATG[C/T]TCTAGTCTTCCTAAG	23077
rs551746953	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77249811	AAATTTAAAAATAAA[A/G]AAGTTAGGTGCTTAA	23077
rs551752745	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77054914	CCAAGATTGATGAAT[A/G]TAATACCTGACATGT	23077
rs551775195	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77110792	TGAAATATTGGGGGC[A/G]GGTTCCCCCAATACA	23077
rs551818751	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77242898	TAGAAGAAGCATGAA[C/T]ACCCTGAATATTTTC	23077
rs551846183	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77226750	ATTACTTTCCTTTCC[A/G]TAACTAAATGCCTAT	23077
rs551848833	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291069	TTGGAAAATTCAATA[C/T]CATTAAAATGGCAAT	23077
rs551874313	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77192657	CATTAATGCATTAAG[A/G]CAGCTGTAGAAGAGT	23077
rs551877707	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77295078	CAGTCACAGGTAATA[A/G]GTCCACACACAGAGG	23077
rs551882359	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77127090	ATCTTGCTATTTGTT[A/G]GTTATGAATGAAATA	23077
rs551887025	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77298855	CATATACCTGCTTAT[A/C]GAATCTACTCAACTA	23077
rs551887222	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77049861	GGCTGGTCTCGTACT[C/G]CTGACCTCAAGTGAT	23077
rs551890687	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77136110	AGGCGTGAGCCACCG[C/T]GCCCAGCCTGTTTTT	23077
rs551893824	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77107735	AGAGTGAAATTGTCT[A/C]AAAAAAATAAATAAA	23077
rs551914582	snp	A/G			intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77325554	TCAAGGAAGCTGAAG[A/G]TGTAGCCAACCCAAG	23077
rs551925374	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77280302	TGCATAGAGTTTCAA[C/T]TGATTAAACACATTA	23077
rs551929823	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77089565	TACCCTGTTCTTCTT[C/G]GGTTTTTAAAATTAT	23077
rs551942882	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77062029	CAATGAACAGGTATA[C/T]TTTGTTACTTAGAGA	23077
rs551943512	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77074523	ATATTTGAAAACACA[C/T]AATTGGTAAAAGACC	23077
rs551946972	snp	A/C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77046417	GAGAGAAAAATATCA[A/C/T]GAGATTGGATGGAAT	23077
rs551947868	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77243338	CTCATTCTGGCTAGG[A/C]ATGGTGGCCCACACC	23077
rs551948018	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77071418	TTTAAGAATCAAAAA[C/T]GATGCTTGGTTTTAC	23077
rs551973110	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77130564	AAACCAAAACCAAAG[C/T]CAACTGCCCCCTAAT	23077
rs552020398	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77259053	TGAGGTCAGGAGTTC[C/G]AGACCAGCCTGGCCA	23077
rs552027563	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77127922	ACCAATTTTTACTTA[C/T]ACAAATATGTACTAA	23077
rs552039804	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77281084	TATTTTACCAAAAGT[C/T]TGAACTTTGAAAGTA	23077
rs552043241	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77321953	ATCACTTAAGCTCAG[C/G]AGTTCAAGACCAGCC	23077
rs552058158	snp	A/C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77158199	ATACTTTCAGATAGG[A/C/G]CTTTACGGAGAAATC	23077
rs552058217	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77165703	TTTGTCAAATACTGA[A/G]GTTAGCCTTTTTATT	23077
rs552076846	snp	C/T	1.67164e-05	0.00289101	intron-variant	MYCBP2	GRCh38.p7	13:77267793	ATAGCTTAACATGCA[C/T]ATTTCTTAAAATTGC	23077
rs552084774	in-del	-/AAT	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77222422	TAAGAAGTTCAACTC[-/AAT]GATATCTCAATCGTC	23077
rs552109767	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77122429	GTCCTTGGCCGGTCG[C/T]GGTGGCTTACGCTTG	23077
rs552118747	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77108263	AACATACTCATAGCA[C/T]ATTATTGAATATATT	23077
rs552128555	in-del	-/AAT	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77205182	AAAAATTAGACATTA[-/AAT]AATAAAATAATAAAT	23077
rs552133105	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77094242	AGATTACCTTCATTT[C/G]TCAGCTGATGAAAAA	23077
rs552138347	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77147334	AATCTGTTTCTTAAT[-/A]AAAAAAATAACAAAA	23077
rs552159063	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77262466	TATTAGGTACCAGGC[A/G]TTATACAATTCACAA	23077
rs552165416	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77215732	GCTAGGACCACTGGC[A/G]TGTGCCACGGCACCC	23077
rs552180138	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77107478	ACAGTGGCTCAAGTC[C/T]GTTATCCTAGCACTT	23077
rs552182878	snp	A/G	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77137715	CGCTTCAGCCTCCAG[A/G]GTAGCTAGGATTACA	23077
rs552198971	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77269901	TATTATCATTTCTGT[C/T]TAAATAGAAGTGATA	23077
rs552203105	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77239156	AGAGTTCTGATCATC[C/T]ATGAAAAACTTAGTT	23077
rs552213425	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77136678	TATTTCAAATATTCA[C/T]TGCATTTCTCAACCC	23077
rs552214953	in-del	-/A	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77322004	GTGTCTACAAAAAAT[-/A]AAAAAACAAGCCAGG	23077
rs552217927	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77108816	TTACACCATTCTCCC[A/G]CCTCAGCTTCCTGAG	23077
rs552220693	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77256669	AAATGCAAATCAAAA[C/G]TACACTGAGATACCA	23077
rs552243077	in-del	-/A	0.0256215	0.110247	intron-variant	MYCBP2	GRCh38.p7	13:77289863	ATAAAATTACTATAT[-/A]AAAATGAGTAGTATA	23077
rs552253074	snp	C/T	1.6492e-05	0.00287154	missense	MYCBP2	GRCh38.p7	13:77098887	GTGCCCCTTGGCTTC[C/T]TCTGATCAGCAGTAG	23077
rs552269490	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77127428	TTCTCTTTTTCCCAA[C/T]TAAATGTAAATAAAG	23077
rs552302094	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77158241	GTACCCCACTGTTCC[C/T]TCTTTTAACCCACAG	23077
rs552309730	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77123142	TGCCAAATCTTTGTA[C/T]TTCCATATTAAATAT	23077
rs552309810	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77284430	TGCCTTCAAATCCCA[C/T]CACCTCAAACCTTAA	23077
rs552325707	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77283783	ACACCTGTAGTCCCA[C/G]CTACATGGGAGGCTA	23077
rs552339929	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77120622	TGTGGACAATAGGGC[C/T]GATTTTGAAGGAGTC	23077
rs552342566	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77175677	AATATTGTTAGGAAA[C/T]AGGCTGGGCGCGGTG	23077
rs552347658	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77229793	AATTGAAGCCTAATT[C/T]CAAAGGCTATAATAT	23077
rs552350107	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77138911	AAAATGTAACCACTC[A/T]CATTTTCTACCTCTT	23077
rs552363807	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77140649	AGCAGGAAGAATACA[A/G]TATGTACCAAATAAA	23077
rs552367090	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77150172	GCTAAAAATCCCAAA[A/G]AGTTCTAGGAGATAC	23077
rs552369215	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77232178	ATACTATATTGCCTA[C/T]GAAATTTTTTTAAAT	23077
rs552381178	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77183930	TTGCTAGGAGTTTAC[A/C]AACTTTTTTTCTTCA	23077
rs552420009	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77113969	TTAAATCCCACAGGT[C/T]CTCATTCCTAAATCA	23077
rs552437558	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77133455	GTGTAATTTTTAATG[A/C]TTAGGAAGAAACAAA	23077
rs552443792	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77114317	CTCAAAGCATGAGAG[A/G]TATTAAGTATTTGCA	23077
rs552457318	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77169146	GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC	23077
rs552476285	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77092935	TTAAGTAATGTCATA[C/T]AATGTAATCTTTAAT	23077
rs552476332	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77240104	ATCTAATTTTGTTTT[C/T]TTATAAAAATTTGTT	23077
rs552484754	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77225966	GTACTAGCCATTTTT[A/T]AAAAATTGCTAATGG	23077
rs552499335	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77141569	TGAGGTCGGGAGTTC[A/G]AGATCAGCCTGGCCA	23077
rs552499496	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77132424	AGATTAACAAATGAT[A/C]CTTTCTCTTCAACTC	23077
rs552504851	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77148717	ACTGATTATTCAAAG[A/G]CATCTAATAAATCTT	23077
rs552518524	snp	A/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77168723	CATTACAATAATTGT[A/T]GGTTACTCTAATAAC	23077
rs552540158	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77200746	CAATATTCAACATTC[C/T]TTAAGAAAAGAATTT	23077
rs552567966	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77270972	TCTTCAACCATATTA[C/T]ACAATAGTTAACCCA	23077
rs552592260	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77155687	ATACCAAACACAGAA[C/T]GTACTTGAGTCTTTC	23077
rs552599282	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77183458	AGTTTTGATAAAATT[A/G]TATTTTTCAAGGAAT	23077
rs552605459	snp	C/T	3.30699e-05	0.00406618	intron-variant	MYCBP2	GRCh38.p7	13:77050983	ATCGTGATTTTAAAA[C/T]ATTAAAAGCATACCT	23077
rs552612589	snp	C/T	0.00279162	0.0372561	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77084664	CAGGAGTATTCATCA[C/T]GCTCACCCCACCTCT	23077
rs552622002	snp	A/G	0.0482946	0.147699	intron-variant	MYCBP2	GRCh38.p7	13:77200101	ATTACTCTGAGCTAC[A/G]GGAGGACATTCAAAC	23077
rs552642846	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77214642	CTGAAATATGTGTCA[A/T]TAGGTGATTCTGTGA	23077
rs552657447	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77285393	ATGTTTTTTATCTCA[A/G]TCTCTCCTAGTTAAG	23077
rs552672925	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77154803	ATCACTATCAGGATA[A/G]CTTTATTTTTAAATC	23077
rs552682038	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77167026	ACACACACACACACA[C/T]CAAATGAAATAATTT	23077
rs552708731	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77221814	GTCATCCCTCAGCAT[C/T]CATGGGGAATTGGTT	23077
rs552719181	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77174149	AACATTGAATTTATA[C/T]ATTAAAAAGAGATTT	23077
rs552727020	snp	A/T	0.00636936	0.0560724	intron-variant	MYCBP2	GRCh38.p7	13:77049774	GTGAGTAGCTCGGAT[A/T]ACAGGTACCCGCCAC	23077
rs552734249	in-del	-/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77129772	TTTTTTCAATTTTCC[-/T]TCCCTTTATAAGTAG	23077
rs552754856	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77215101	TCAAGGATATGGGAG[A/G]AAGTGACACCTCTTG	23077
rs552760556	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77194701	GGGTGGATACTAACA[A/G]TTCCCATCTCACAGT	23077
rs552779814	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77092124	TATATGTCCCATTGC[A/G]CTCATTAAAGTATTT	23077
rs552788301	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77314306	CCACACAAAAACCTG[C/T]ACACAGATGTTTAGA	23077
rs552792981	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77183813	TCAGCCTCCCAAAGT[G/T]CTGGGATTACAGGCA	23077
rs552813035	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77056784	GTTTAACAGAATGTA[A/G]TCAGTTTTAAATGGA	23077
rs552831639	in-del	-/A	0.00597247	0.0543191	intron-variant	MYCBP2	GRCh38.p7	13:77304991	GTCTTCTATATATTG[-/A]AAAAAAACTGGATCC	23077
rs552831890	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77181542	ATTTAAAATAATCAT[A/T]TTGTAAATATACTTA	23077
rs552831982	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77213475	AGAGTGAGGCTCTGT[C/T]TCAAAAAGAAAAAAA	23077
rs552833602	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77113161	TTGGAATGCTCCATT[A/G]ACCTCCTTCCTCATC	23077
rs552836964	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77242010	CTTCCATAACAATTT[A/G]TCTTAATCCTACAAA	23077
rs552848523	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77193902	AAGGTGTATAAAATA[C/T]ATGCATATTTCCATT	23077
rs552854566	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076108	GTTTTAGTCAGGACC[A/G]AAAAAGTAAAGCAAC	23077
rs552855730	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77199333	ACTGCACTTTTCTGA[C/T]GGGCTTAAAAAACGG	23077
rs552866776	snp	C/T	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77210443	GTGATCTGCCCGCCT[C/T]GGCCTCCCAAAGTGC	23077
rs552875528	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77240857	CCACTCAAGAAAAGA[C/T]ATTCACTATATATTG	23077
rs552895796	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77174829	AGCTAGTAAGTGATG[A/G]AACTAGGTCTGAACA	23077
rs552917362	in-del	-/TT			intron-variant	MYCBP2	GRCh38.p7	13:77163194	CCCTTCAACATACAC[-/TT]TTTGAGTATTTGTGC	23077
rs552950802	snp	G/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77069308	CATGTTGTAGTTCAT[G/T]GAAAAGAATAATAGT	23077
rs552962710	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77276771	TCCTGGGCTCGAGCG[A/G]TCCTCCCACCTTAGC	23077
rs552986472	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77091786	AAGTGCAGTGACACA[A/G]TCGTAGCTCACTGTA	23077
rs552987935	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77057565	TGTATAGATCAATTA[C/T]ATAATGTTGTAAAAA	23077
rs553002397	snp	G/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77233515	TACTCATAAAATTAT[G/T]GTGTAGTTACTAATA	23077
rs553007424	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77146523	AGGAAAAGCTTCCAC[C/T]TTGGAGAAGGAGATT	23077
rs553018750	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77132563	ACAGAAACTCAATTC[C/T]GTAAGAATTCAGATT	23077
rs553020590	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77283029	ACCACCCTGTAGTTA[C/T]GGATATGCCTTACTA	23077
rs553041125	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77318611	ATACAAAAATCAGCC[A/G]AGTGTGGTGGGACAC	23077
rs553098762	snp	A/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77240195	GTCATATCAGAATAG[A/T]TTTTTAATTACTTAA	23077
rs553121802	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77142446	ATATCTGAGTCTATA[C/T]AGTTACATTAATGTA	23077
rs553130338	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77309179	CCCATGTCCAGCCTC[A/C]CTTTCCCACTTTTCC	23077
rs553153936	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77124558	ATGAGCAACTAGTAT[C/G]TGTCAAAACTGTTTC	23077
rs553155379	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77106924	ATCTTAACTAAGATA[C/T]TGGCAAGAGCTTGAG	23077
rs553188658	snp	A/C			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228805	TTATATGTATGTACA[A/C]ATTATATATAATTAT	23077
rs553190597	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77195872	TTGGTTTCTCATCTC[C/T]TCCACAGCATGATAT	23077
rs553196327	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77160317	ATGATCGTGGGCGAA[C/T]TGCCTAAATGCTCTA	23077
rs553201594	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77083618	GTCACTAACTCATAC[A/G]GCATTTTTATGTGAA	23077
rs553208568	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77199781	CCCACAGCAGGGGCA[C/G]ACTGACACCTCACAC	23077
rs553211129	snp	C/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77155208	TTATTTTTTACTTAG[C/G]TAAGATGCTACATTG	23077
rs553221722	snp	A/C/T	0.000164727	0.00907404	intron-variant	MYCBP2	GRCh38.p7	13:77140801	AGCATCAGTGACAAA[A/C/T]GTAAAAATTGAATGA	23077
rs553227614	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77226352	TAGCATCAAAAACCA[C/T]ATTCCAGAATATAAA	23077
rs553229663	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77116292	TTTTACTAAATAGCA[C/T]AGGGAAGTTCACTAA	23077
rs553229975	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77232929	GGACAAGGAAAAGAT[A/G]TATTGTAAAATATCT	23077
rs553261435	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77299836	AGAATTGTGGTTGAC[A/G]ATAAAAGGAAAAGGC	23077
rs553266243	snp	C/T	0.000149989	0.00865863	intron-variant	MYCBP2	GRCh38.p7	13:77263899	AAGGAATTCCATTTA[C/T]ACTAGCTACTTAAGA	23077
rs553318565	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77154423	GAAGAGAGGAAAAAA[A/C]AAAGCAGATCCATCA	23077
rs553323083	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77139980	AACTCAGTAACCTTA[A/T]TATTATGCAAACAAT	23077
rs553324898	snp	C/G/T			intron-variant	MYCBP2	GRCh38.p7	13:77144920	CAAAGCTAGTCCCTC[C/G/T]CCTTGTGCTGTGAAT	23077
rs553333925	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77251499	TTTGAGTAACAAAAA[C/T]AAATTTTAATTTAGG	23077
rs553335683	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77243035	TGGATTTTCATGTAC[C/T]TTTTCTCTGTAGCTA	23077
rs553336405	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075635	CACACATTTAATAAC[C/T]TGCTTTTATACTATA	23077
rs553354552	in-del	-/AGAG	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77233860	TATATGTATACACAC[-/AGAG]AGAGAGAGAGAGAGA	23077
rs553356491	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77184468	TACTTGAAAAGAATA[C/T]GTATTTTGCAGTTTC	23077
rs553369943	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77193409	ATCCTTGTTTCTGAA[A/G]ATATACATTTTCACT	23077
rs553378644	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77094704	TCGCTTGCCTGACAG[A/T]TTTCTATTTATCCTT	23077
rs553379576	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77217191	AGCTGTAAATGTCAT[A/C]TCAGACACTTAGGTT	23077
rs553385480	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77292657	AGGGAGGGATGGAAT[C/G]AGCAGAGGGTAAGAA	23077
rs553395773	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77109399	CAGGAAGTAGAGCTG[A/C]GACAGTAATGCTCTC	23077
rs553404140	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77254920	TCCATGTTTCTGCAA[A/T]TAACAATATTTCATT	23077
rs553412744	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77285646	ACAAAATTAGCCAGG[C/T]GCGGTGGCACATGCC	23077
rs553414512	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77170102	GCTGTATCAGTGACA[G/T]TAGGCAAATTACTTA	23077
rs553416649	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77224785	CCATTTAATAACATT[A/C]ATTCTTATTAACACA	23077
rs553420617	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77156641	ATGGCCCTCTACTTG[C/T]CTGACAGCAGCCAGG	23077
rs553439658	snp	A/C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075138	CATTGAGCCCGGGAG[A/C/G]TTGAGGTTGCAGTGA	23077
rs553455159	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77086977	CTTTAAGCATATTAA[A/C]ACATTATTCTACATT	23077
rs553461145	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77063158	TTCTAGATAATAAAA[G/T]TTCCTCAGAAGTCTT	23077
rs553481860	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77157112	TTTTTTTTGAGATAG[A/G]GTCTTGCTCTGTTGC	23077
rs553497106	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77243604	GGCAACAGAGCAAGA[C/T]TCCATCTCAAAAAAA	23077
rs553509675	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77274661	TTTATTTTACTTCCT[A/G]ATGGATAACTCCACT	23077
rs553516339	snp	A/G	1.93695e-05	0.00311197	intron-variant	MYCBP2	GRCh38.p7	13:77185061	GAAGAGTATTAAGCA[A/G]TATATCAGATTTTCA	23077
rs553517391	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77169328	GTGAACCCGGAAGGC[A/G]GAGCTTGCAGTGAGC	23077
rs553518340	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77175980	TAATAATAATAATTA[A/T]AAAAAAATAAAGAAA	23077
rs553518758	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77184981	TAAGTCATGTACACC[A/G]AATGATTTCCTAATT	23077
rs553545388	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77236833	GGCCCAGTTGTTCGA[A/G]GCCAGCCTGGGCAAC	23077
rs553545993	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77224176	ATAATTGCTAAGAAT[A/G]TAGTGATATTTTGTG	23077
rs553552212	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77128367	AGCAAATATCCATAG[A/C]TTTAGCAAAAAAACC	23077
rs553573652	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77323391	ACTCATCATGTTTTT[A/G]TTTCTTGAACACAAG	23077
rs553574511	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77278402	TTCAACTCTTAAACC[A/G]TAACTTCAGTGGAAC	23077
rs553589393	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77209500	TGGTAACTAAGTCTC[C/T]TGAACATTGACTTCT	23077
rs553607085	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77256701	CTCTCCCCAGTTAAC[A/G]TGGCTTTTATCCAAA	23077
rs553628516	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77240821	CAAGGACTGTGATAA[C/T]TGAGGTTCATACTGA	23077
rs553629503	snp	A/G	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77177300	GGAACACAAACAATC[A/G]GGTAAAATCATTATT	23077
rs553648352	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77172485	TTTATCAGATCACTC[C/T]GGCTGTGCTGTAGAG	23077
rs553660405	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77060093	ATTCCTACCTCAGGA[A/T]CTCTGCAATTTGAAA	23077
rs553683971	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77188533	TTCTTCATGTGTACA[A/G]TGGGGATGGCAAGTG	23077
rs553701635	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228386	GTGGTGAATACCTGC[A/G]GTCCCAGCTACTTGG	23077
rs553721771	snp	C/T	0.00478085	0.0486577	intron-variant	MYCBP2	GRCh38.p7	13:77059057	CGCATCACCAAAATG[C/T]AGATTTTTTTTTTTT	23077
rs553727844	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77216238	AAAATACAAATACCT[A/G]AGTCTATACCAATAA	23077
rs553728233	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77281448	ATTATAACAATAAAA[A/G]AACACAAGAAGCTTC	23077
rs553728631	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77159303	ATAATACATTGCCTA[A/G]CAAATAGTAAGTGTT	23077
rs553738498	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77055041	ATGGTAGGTGAAGGT[A/G]TAGATGTAAAAGAGG	23077
rs553754798	snp	G/T	0.0150606	0.0854603	intron-variant	MYCBP2	GRCh38.p7	13:77119462	CGAGCCATATATCTT[G/T]TTTTGAAATAATAAA	23077
rs553767075	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77271121	CTTTTATTACTTTAA[C/G]CATACTTTATATATT	23077
rs553776644	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77188012	GGACGCGGAGGTTGC[A/G]GTGAGCCAAGATCGT	23077
rs553781947	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77268041	GAGGTACAATAATAC[A/G]TCAATATTGATGTCT	23077
rs553783109	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77296424	AGGCAAGAAAGAAAA[C/G]AAACACCCAAAAGAA	23077
rs553787931	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77158350	AGAGATCTGCATGCT[C/G]GATAAAATGGTGTAT	23077
rs553791011	snp	A/C	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77123220	TGATTTAAAGGCACT[A/C]ACTTCATATCATTTC	23077
rs553800218	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77152837	TTTGGAGTCTGAGGC[G/T]GGCGAATCACAAGGT	23077
rs553806570	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77306287	AATGATACTCCTATC[A/G]TGTTCAAGCATCAAT	23077
rs553822154	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77119451	AACTGTGTACACGAG[C/T]CATATATCTTTTTTT	23077
rs553847025	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77206342	ATATACATAAATTAA[A/G]TATTATATACTTGAA	23077
rs553861749	snp	A/G	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77152383	CTTTAAACAATTAAA[A/G]AATCTGAAGATGATA	23077
rs553862205	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77144048	TAAAAATGCATTCAT[C/T]CATCCATATTTGCTG	23077
rs553867729	snp	A/C	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77305252	CTATGAACATAGAAG[A/C]AAAAATACTGCACAG	23077
rs553888324	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77282096	AGCAGAAAGAGAGGA[A/G]GAGAAGGCTAAGATG	23077
rs553900062	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77190507	TGAATGGGTTAGTCA[A/G]TAAAATGAAAGAACT	23077
rs553907713	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77078015	AAAACTGTTCTTATG[C/G]CATTTAATAACCAAG	23077
rs553952144	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77198012	CGTTGTTCACTATTC[C/T]GAAAAGAAAAAATCT	23077
rs553959363	in-del	-/TA	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77154956	AGCATATTATGTATG[-/TA]TGTGTGTATGTATAT	23077
rs553967226	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77152633	AGCAACTGATGAGAC[A/G]CGCGGCTTAACCTCA	23077
rs553975350	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77078996	CTTCTGCCTGTCTCT[G/T]ATGGTCCTTCCTGAT	23077
rs553982577	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77186470	CACTGTAGTAAAAAA[G/T]AAAATAGAGTTTTAG	23077
rs553988548	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77298377	TTATGTTTCATTGTA[C/T]AGCCAATAACTGTAA	23077
rs553989315	snp	A/G			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77086426	TATAATTTGTCCACC[A/G]TGATTTGTATTTATT	23077
rs553997237	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77277786	GAATTGAGAACCACA[A/T]AATGAGAACCACAGC	23077
rs554011037	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77120059	TTTACTGTGATAGCT[A/G]TTAGTACAATGACAG	23077
rs554011401	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77063325	CACTTTGGGAGGCCA[A/G]GGTGGGTGGATCACC	23077
rs554031972	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77303546	GGAAAAATTAAACGA[A/G]AAATTAAAAAAAAAC	23077
rs554041612	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77319154	CCCTTCCTCCCTTCG[C/G]AGATCCAGCACCCCG	23077
rs554046060	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77080015	GAGGGAGAGTATGTC[C/T]TTGCTTAAAATGTAC	23077
rs554058427	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77180751	AAGACTTTGTCTCTA[C/T]AAAATGTTTTTTTAA	23077
rs554064028	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77229192	TCCTAGCTTTCCTAT[C/T]TATAATATAGCAACA	23077
rs554064585	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77064233	AGGAACAACCAGGCA[C/T]AGGCAGGGGTCTTGT	23077
rs554101405	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77212550	ACATAGTAAGTTGAT[A/T]GTATAAAAGAAAGTC	23077
rs554119756	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77327958	TTGTTCCAAGCTAAC[C/G]TACGAACCCCATCTA	23077
rs554120551	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77236916	GAATAATGAATACAG[A/G]TGATGCTAGAGGAAA	23077
rs554122422	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77230542	TATACATTATGAGAT[A/C]TCTTGGGGATGGGAC	23077
rs554123468	in-del	-/AACAT	0.468349	0.121752	intron-variant	MYCBP2	GRCh38.p7	13:77317939	AAGACTCCGTCTCAA[-/AACAT]AACATAACATAACAT	23077
rs554136262	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77220135	TGTTTGCGGTTTTAT[C/T]ATGTCCTAGCACCAC	23077
rs554149030	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77283324	GAGTCCTTTCTCTAA[C/T]GTGTTCCACTATATC	23077
rs554170657	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77105020	GCAGCTATTGTTAAA[A/G]TATCAGTTAGGAGGG	23077
rs554178226	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77166178	CTTGCCCAGGGTACC[C/T]TATTTATTCCTCGAA	23077
rs554209039	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77220836	GCTTAAGACTGAAGC[A/G]GTCTTGATGAATATC	23077
rs554211746	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77213388	GCTGAGGCATAAGAA[A/T]TGCTTGAATCTGGGA	23077
rs554230155	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77104018	GAAGCACTTAATTTA[C/T]CTTTTTTTGAAGAAT	23077
rs554241019	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77079044	TCCAACTAACCACGG[C/T]TCCTATAACTTTAGT	23077
rs554248459	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77219314	ACTCGATTTAGCAGA[A/G]GGAGGTCTCTTTGGT	23077
rs554257418	in-del	-/GGAAACATTG	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77055410	TAAACAAGTTTTACT[-/GGAAACATTG]GGAAACATTGTACCA	23077
rs554262430	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77313763	TTTTTTCCCCATCTC[C/T]TCAGTTACACCCTCA	23077
rs554275723	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77136715	TTAACTCATTCTTTT[A/G]ATTCTGAACTGATCG	23077
rs554282281	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77237713	CACCAATATCTATCA[C/T]AGTATGAAATTATAT	23077
rs554285352	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77248262	AAAAACAATAGACAA[C/T]TGGACTTCATGAAAA	23077
rs554294483	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77268098	AGAACATTCCTCTCA[A/T]TTAGAGGAAAAGTCA	23077
rs554307705	snp	A/C	3.30213e-05	0.00406319	synonymous-codon	MYCBP2	GRCh38.p7	13:77096438	TCCTCCACAAAAATG[A/C]CCAATGCTATTGTAA	23077
rs554321822	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77246474	AAGAAGAAGAAAGAA[A/G]AGAAGAAAGAAGAAG	23077
rs554384933	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77198678	TGGATACGAATAGGT[A/G]TGGTAACATATGACT	23077
rs554400625	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77152473	TCTCAAGCCTGGAAA[A/C]CATGACCCTAAATGA	23077
rs554414416	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77128572	TTTTATTGAAAAGGT[A/G]ATAAAACTATATTAA	23077
rs554425093	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77112857	TTGATATACTTTTTT[C/T]TCCATTAACAAACAA	23077
rs554442804	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77097086	ATGCCACTGTTTCTG[C/T]TGTGTGAGACAGACA	23077
rs554446441	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77301251	GAAACCCCGTCTCTA[C/T]TAAAAATGCAAAAAA	23077
rs554451361	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77166209	TGCAATCCAGATACA[C/T]AGTAGGTCTTTAATA	23077
rs554461874	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77268757	GCATTCCAGCCTCAG[C/T]GACAAGAGCAAAACT	23077
rs554461980	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77260372	GATATGTCTTTGTCA[C/T]ACATAACTAGTATTG	23077
rs554479109	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77138517	ATCCTAAAGAGCACA[A/C]ACATTTGATGGTAAT	23077
rs554490366	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77221121	GCATCTACCAGTTAC[C/T]ATACCACTGTGTAGA	23077
rs554505421	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77189474	CGGTGCATAAAAACC[A/G]AACAAACGAAAAAAC	23077
rs554506547	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77275257	GTAATGAAATAGAGA[A/C]TGACTTTCCATTCCT	23077
rs554515465	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77281565	AATTTTACCTTTACT[A/G]CTGCTCTCAAATAAT	23077
rs554558316	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77118625	CCAATTCAGAAATGA[C/G]TGAAAATTGGTGACT	23077
rs554559022	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77180834	CTGAGGTGGGAAGAT[C/T]GTTTGAGTCCAGGAG	23077
rs554559063	in-del	-/A	0.0341408	0.126114	intron-variant	MYCBP2	GRCh38.p7	13:77247935	ACCTAAAACTATTAC[-/A]AAAAAAAACAAAAAA	23077
rs554581835	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77090603	TCAGATATAATCGTA[A/G]GTGCACCAAATAGAA	23077
rs554607991	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77288585	GCAATAACCAACCAA[C/T]CTGACAAGGGCTGGA	23077
rs554617511	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77146381	TTATTAAAGATAAAT[C/T]CTACAAGGTTTGAAG	23077
rs554619439	snp	C/G			intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77325697	CTCTCTACTCTAAAG[C/G]CTGTAAGTAACAGAG	23077
rs554632296	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77129284	GAAAGGGAACAGGAT[A/G]TCATCTGCAGAAGAT	23077
rs554647430	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77233626	AAAGTCAGTAAACCA[C/T]GTATTCGTTGAAGAC	23077
rs554664065	snp	C/T			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77085620	CCTTGTGAATTATAC[C/T]AGCTAATGGAAGGTG	23077
rs554671110	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77290149	AACATCATTAGCTAC[C/T]AGGAAAATGCAAATT	23077
rs554688400	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77260792	GTCAATTAATATTTA[C/T]GCTATCATTGCTAGA	23077
rs554695677	snp	G/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77137449	GGGACTTAAGAAAAT[G/T]TTCTTAAATAAAACA	23077
rs554695967	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77096752	GTATATTTAGATATA[C/G]TTAATTATGTCAATA	23077
rs554703118	in-del	-/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77239831	ATTAAAATAAAAATA[-/T]TTTTTAAAAAGCAAA	23077
rs554705484	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77284232	ACTGTCTTAATCATG[C/T]TAAGGAAAAAAAAAA	23077
rs554705916	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77319407	CAACCAGAACACTGA[C/T]CTTAGCATAGCTGAG	23077
rs554720289	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77328848	TACATGAGATTGAGG[A/G]AGGACTTAAAGGATC	23077
rs554721195	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77258034	TCCTAAAACATTATC[A/G]TCCAGACTTGGGACA	23077
rs554721334	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77172509	TGTAGAGAACTGATT[A/G]TAGGAGACCAATAGT	23077
rs554734893	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77138603	TTATTATACTTCATG[A/G]AGTAGCAATCTTGTG	23077
rs554738824	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77156053	TTTAATCCAGTTATA[A/G]TTACCTTCATATTGG	23077
rs554745141	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77190733	TCATACAGTCCAGGG[A/T]CAAAGTAGTCACTTA	23077
rs554767717	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77245602	CACATACTGGGGCCT[C/G]TTGGGGGGTGGGGGC	23077
rs554790174	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77298533	CAACGAGTATTTTAA[A/G]AGAAAGAGAAAGTAT	23077
rs554794871	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77130163	CACAATTTTATTGCT[C/T]ATGTAAATATTATGA	23077
rs554797745	snp	A/C	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77072216	GAATGGCGTGAACCC[A/C]GGAGTCAGAGCTTGC	23077
rs554800950	snp	C/G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77110791	TTGAAATATTGGGGG[C/G/T]GGGTTCCCCCAATAC	23077
rs554831328	in-del	-/CTAT	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77138985	TTTACTACTTCCTGC[-/CTAT]CTGTGATGGATCATA	23077
rs554837041	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77073081	GATATGTGCAACTAT[C/T]GTCGTCAGTCAATAT	23077
rs554839687	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77089128	AAGCCTTTGTCATTG[G/T]TTTTTTGAACATGAC	23077
rs554857147	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77169063	ATCTTTCCTTACATA[G/T]CATATTCCTAAAATT	23077
rs554871871	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77130278	CAAAATTCCTTATCA[A/G]TTATAAGTCATTTTA	23077
rs554899957	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77206440	CTCTGTGAAAATTAA[A/C]TAATTGGGCATACAT	23077
rs554900189	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77313849	AAGATGGGGCAAAGA[A/C]CTTAACAGACACCTC	23077
rs554906748	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77182777	AGGAGGGCGGGGAGG[C/T]CTAGGACTTCCAGTG	23077
rs554909859	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77295407	AAAGTGCGGGGATTA[C/T]AGGCGTGAGCCACTG	23077
rs554918267	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77312891	AATATAAAAACATAA[A/G]CATCCAAACAACACT	23077
rs554924734	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77055878	GATAACCAGACAGCA[C/T]ACATATTCTAAATAA	23077
rs554924989	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77069269	CAATGAAACACTGCT[A/G]GAAAGATAAAGCAAA	23077
rs554933016	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77173387	AATGTACTATTTATT[G/T]TAGTGCTTATGTAAC	23077
rs554969237	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77198700	CATATGACTCTCAAT[G/T]ATTTTTAGTTGGCCT	23077
rs554970028	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77200322	ATAAATGAAGTGAAG[C/T]GAGAAGGGAAGTTTA	23077
rs554972749	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77264302	ACCACGATGAACAAA[A/C]TATAATGTTGGTTAC	23077
rs554980227	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77132577	CTGTAAGAATTCAGA[G/T]TATATGGGAACTATA	23077
rs554984951	snp	A/C	0.00676609	0.0577691	intron-variant	MYCBP2	GRCh38.p7	13:77179073	TGTATGCGATGAACC[A/C]TATGTATGCGAATTT	23077
rs555017660	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77130011	TTAATTCACAGAAAC[A/G]TTATCCTAGAAAAAT	23077
rs555032645	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77045750	TAGAGAGGATCACTT[C/T]GAGCTACAGATCTTT	23077
rs555051250	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77160048	TATGATCAGAAGACA[G/T]TGTTCAAAATCACAA	23077
rs555062108	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77052532	AAATGGATTCAAGCT[C/T]AAAGTAGGCAGTTAC	23077
rs555066833	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77238407	ATTGAAGTTTAATTT[C/T]CCTTACGAAACAGAG	23077
rs555067970	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77102525	ATAATACTTTAAGAC[A/G]AAATATTTAAGTAGG	23077
rs555083719	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77306602	AGAGAACTCTCTGAA[A/C]AGCTTTGGCTATAGA	23077
rs555086257	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77210974	ACCTAGGTAGTGTTG[C/T]TTAAAATGCATGCTC	23077
rs555090500	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77108940	CCTCGTGATTCACCC[A/G]CCTCATCCTCCCAAA	23077
rs555095896	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77089668	TTTTTTTTTTTAAAT[C/T]GATTAAGGGCTATTT	23077
rs555108676	snp	C/T	0.00953873	0.0683987	intron-variant	MYCBP2	GRCh38.p7	13:77287138	GTGATCCGCCCGCCT[C/T]GGCCTCCCAAAGAGC	23077
rs555127477	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77302313	AAAGCAGCCAGAGAA[C/G]AGATATGCTTAAAGG	23077
rs555180447	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77257615	TTCACTATGTTGTTC[C/T]GAAAAACTAATGAAA	23077
rs555184193	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77186515	AACAGTATCAAATAA[C/T]TTATTTTATGTCTAT	23077
rs555221091	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77287656	TAAGCTTAGGCAGAA[A/G]GGAAAAGGCTCTCAG	23077
rs555234922	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77080856	TTGAAGCAGGAGAAT[C/T]GTTTGAACCTGGAGG	23077
rs555254525	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77073920	TCATGTTCACAGATA[C/T]GAAGACTCAATATTA	23077
rs555257667	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77179167	TGTATATATTGGATG[A/G]GTTAATTCAGAATAG	23077
rs555287317	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77130747	CTCCCTTACAAAGCA[G/T]AGTGGGACAGACTTT	23077
rs555306447	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77236301	ATAACCAGGTTTAGA[C/T]AGAAGCTACACTCAT	23077
rs555310992	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77195649	GCCATTACTGTATCT[A/G]TTCTCTTACTGGTAC	23077
rs555325575	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77061518	AACTTGCTATTTATA[C/G]ATGGTAAGCGAGACA	23077
rs555371423	in-del	-/CCAC	0.00438332	0.0466095	intron-variant	MYCBP2	GRCh38.p7	13:77064130	TTTCCTCAAAGATTT[-/CCAC]CCTGACCCTGCCCTG	23077
rs555375350	snp	C/T	4.14156e-05	0.00455039	intron-variant	MYCBP2	GRCh38.p7	13:77099117	GCTACAAAATTTATA[C/T]TGTTTGTCATACATA	23077
rs555377387	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77309607	ATATTTGCACTTGAG[A/T]TCTAGTCACCTGCTA	23077
rs555386823	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77069622	AGCACTTTGGGAGGC[C/T]GAGGCGGGTGGATCA	23077
rs555399379	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77054445	TGCAACAGAGGAATT[A/C]GGGGTTCTACACCCG	23077
rs555403044	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77134899	TTAACGATGAATACA[C/T]GAATTCTAAAACATG	23077
rs555412121	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77142118	TACTGAAATTTTACC[A/G]GAATTTTTAGAGAAA	23077
rs555424604	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77099924	TTATGCTTTTCTTTG[A/T]GGCATTAGAGCCAGG	23077
rs555431485	snp	A/C/T	6.87703e-05	0.00586354	missense, utr-variant-5-prime	MYCBP2	GRCh38.p7	13:77273632	TTCATCCCAGTACTT[A/C/T]GAACGGTGATTTCCA	23077
rs555431815	snp	A/C/T	0.000399281	0.0141238	missense	MYCBP2	GRCh38.p7	13:77212091	CATATTTTGATCCAA[A/C/T]GTTAGGCATGGGAGC	23077
rs555442619	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77249479	AATAATTAATTTCAA[A/C]AGGGACCAGATAATT	23077
rs555444857	snp	A/T	0.00755907	0.0610114	utr-variant-3-prime	MYCBP2	GRCh38.p7	13:77044915	TGTTTTTTTTTTTTT[A/T]AAATAACAGTCTAGG	23077
rs555452216	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77318423	TGAAAAAATAACACA[C/T]AAATTGGAAGAAAAA	23077
rs555465669	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77241310	TTTTTAGAGGGAAGA[G/T]AAAAAGAGTAACAAG	23077
rs555483854	snp	C/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77202184	GAAGAATCAAATAGA[C/T]GCAATAAAAAATGAT	23077
rs555490810	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77226859	GCCTGTGTGGCTTAC[C/T]GGAAACGTCTTAATC	23077
rs555499828	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77094849	TGTAGCACTCCTCAC[A/G]TGGCATTTCAAATGT	23077
rs555504048	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77205239	CAAAAAAGGACAACA[C/T]TGTTGATGAACTTTA	23077
rs555519318	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77280481	TCTATTCTCAAGCCA[A/G]TGGAAGACTACTATA	23077
rs555537937	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77157669	GCACAAGAATCGCTT[C/G]AGTCCAGGAAGTGGA	23077
rs555541348	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77212482	GTACGACAAATACAC[A/G]CAATATGTTAAAATA	23077
rs555543215	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77203242	CATAAGCATTCTTAT[A/G]CACCAACAACAGACA	23077
rs555545828	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77195573	CTGCACTCCAGTGTG[A/G]GCTACCAAAGAGACT	23077
rs555587730	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77242404	CAGGCGTGAGCCACC[A/G]TGCCTGGCCAGTTAA	23077
rs555603145	snp	A/G	3.81563e-05	0.00436769	intron-variant	MYCBP2	GRCh38.p7	13:77164593	TTTGAATGATAATAC[A/G]GATTATCAACAAAAT	23077
rs555620843	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77251677	ACAGACCAAAGAAAG[C/T]CTCCCAACCATGCTC	23077
rs555636838	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77093922	AAAAAATCTATAATT[A/G]TGCTGTGTTAGCATT	23077
rs555659909	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77282194	GGTTGGGAGATCACC[A/T]GAGGTCAGGAGTTGC	23077
rs555667591	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77126037	GTGATGATAATCCAT[G/T]ATGGTATAGTACATT	23077
rs555695122	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77301974	CACAGACTTGCAAAC[A/G]GGCCAAAAATAAATA	23077
rs555717261	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77279578	TTCAAGAAGTATTAA[C/T]TAAATTGTTTGGAGA	23077
rs555719931	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77247451	TAAGTAGAAACACAT[C/T]TATGTTCATGGATTA	23077
rs555720371	in-del	-/T	0.0166325	0.0896639	intron-variant	MYCBP2	GRCh38.p7	13:77210618	CTCTACCAGTAAGAG[-/T]TATTTTTTAATGCAC	23077
rs555731630	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77249952	TTCATGGCCGGGCGC[A/G]GTGGCTCACGCCTGT	23077
rs555747495	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77243705	ATACATTAATTATTA[C/T]CCTAATTTATTAACA	23077
rs555748703	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77235148	TGAAATGAATATAAT[G/T]ACAAAGATACAGGTC	23077
rs555764320	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77197425	GGTGGATGGTACTAA[C/T]CATGAGAGAGAGAGA	23077
rs555790466	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77047602	AAAAAGCAGTTGGGG[A/G]AAAAAAGTCAAGCTG	23077
rs555807199	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77303914	AAAGCAGACATTCAA[C/T]AGAGGTTATCAGGGA	23077
rs555825869	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77287183	TGAGCCATTACGCCC[A/G]GCCAGTTTCTTTTTT	23077
rs555827013	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77310898	CTGGTTCCAGTACAT[G/T]GGCATAAACCCCAAA	23077
rs555851936	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77053766	CATCTCTCTACTTAG[A/G]CATCCATTCATCCTC	23077
rs555882168	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77150343	GATGGGGTCTCACTA[C/T]ATTACTGAGGCTGGT	23077
rs555896818	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77048223	GAGAGGCCCCCTGCC[C/T]TTCCACGACAGCAAG	23077
rs555914915	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77101798	TGGGGTAAGCCCCTG[C/T]GCTAATTTATGTTTA	23077
rs555931414	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77210563	CCTTATTTATCTCTA[A/T]GTTTTTATAATTTCC	23077
rs555939039	snp	C/T	5.49425e-05	0.00524102	intron-variant, missense	MYCBP2	GRCh38.p7	13:77118462	AGATTGGGTCGTGAC[C/T]GAATGGAATTCAATA	23077
rs555949569	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77295451	ATATCATTTCATCCC[C/T]GGATCCATCTGTGTC	23077
rs555950182	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77071537	TTTTGGAGTCCATTA[A/G]AATGTTGAGATCAGC	23077
rs555951699	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77243005	TTTCAGTGGTTTCAG[A/G]ATAGGGTAGGAAAGT	23077
rs555952629	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77135625	CAGATCTGTTTAGAG[A/C]CCTATGCCAATTAAT	23077
rs555986487	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77046461	TCAATGAGGAATGAC[A/G]TCTCATTTACTTTAC	23077
rs555993687	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77173900	AAGATTCACAGACAT[C/T]AAAATATTCTGTGAC	23077
rs555995985	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77151008	TGTCACTGACATCAA[A/C]ATAAGCAACTTACTA	23077
rs555999021	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77256286	AAATTTAAAACATGT[C/T]GTGTAACAGCAGCTA	23077
rs556014445	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77247786	TCAGATGATTTTTGA[C/T]AAAGGAGCCAAGATG	23077
rs556032470	snp	A/C/T			intron-variant	MYCBP2	GRCh38.p7	13:77295161	TTATTTTTGAGACGG[A/C/T]GTCTTACTCTGTCGC	23077
rs556041536	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77180027	GGTTGCTAATCCAAT[C/G]TGAAATTAGCTTCCA	23077
rs556057130	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77296501	TTACTTCAGCACATA[C/T]TAATAAAATGGTTTA	23077
rs556062484	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77281305	GGTATATTTTGGTTA[A/T]TGGTATTTCAAATAT	23077
rs556070505	snp	C/T			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77293037	GAACTTTGACTGCAG[C/T]AGTGCTTCTATGCAT	23077
rs556074799	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77144843	GTTGCAATGTGATTA[A/G]TAAACCTACTTTCCC	23077
rs556084387	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77097101	CTGTGTGAGACAGAC[A/G]CATTAATGGCACACC	23077
rs556104686	snp	A/T			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77086629	CTTGTATTTTTTATT[A/T]ACTTTTTCTGTGTTG	23077
rs556127831	snp	A/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77054529	AGATGTAATGGAAAG[A/T]AAAAAGGACTCAAGA	23077
rs556127891	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77188742	GGCCAATTCATCTGG[A/T]CATGTTAAAATCATA	23077
rs556128784	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77143538	GCTTCCCTGGTTCTG[A/G]GGCTACCTGCATCTC	23077
rs556130903	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77151628	GCAAAAAACAGATTC[A/G]TTAATGGATGTTAAT	23077
rs556135161	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291903	TTGGCTAACCTTTGG[A/G]AATGTGGATGTTTAG	23077
rs556172480	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77327160	GCCCCTTTTCCTCCC[C/T]ACCCCCTCTCCGCCA	23077
rs556176750	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77048462	AGAGAATTGCTTCTT[C/T]TGTCCTTCTAAGTAA	23077
rs556181004	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77164718	GTGGCTCAGGCTGGT[C/T]ATAAGGTTCAGGTTT	23077
rs556199174	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77070286	AAAAGCCTTCATAAA[C/T]TTTTCAAAATACTTT	23077
rs556199514	snp	C/G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77055275	TGAGAGAAGTTTATT[C/G/T]GAGAAGGAATTGCCC	23077
rs556206561	snp	A/G	0.0150606	0.0854603	intron-variant	MYCBP2	GRCh38.p7	13:77202218	GGGGATATCATCACC[A/G]ATCCCACAGAAATAC	23077
rs556208175	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77209177	GAGCTGGCAGGGCAT[A/T]TGAGATCATCTGTCC	23077
rs556228335	snp	G/T	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77094586	CACATATTTCCTCCA[G/T]TAGCCAGTCCTTTAA	23077
rs556230371	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77242559	GAGGTTTTTCCAAAA[A/G]AGGACACATGAAAGC	23077
rs556231755	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77127319	ACTTCTAAAATGAAA[A/G]AACCTTCCCTAAATT	23077
rs556245345	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77240086	TGTAAGTATATCATA[C/T]TCATCTAATTTTGTT	23077
rs556255849	snp	A/G	1.64732e-05	0.0028699	synonymous-codon	MYCBP2	GRCh38.p7	13:77150821	TGATGCCAGCCCTCC[A/G]TAAGTCATGTCAGTA	23077
rs556264740	snp	G/T	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77055010	TCAAAAATTTTGGGG[G/T]GTCATAAACATATAC	23077
rs556309650	snp	C/G	0.000399281	0.0141238	missense	MYCBP2	GRCh38.p7	13:77188975	AGTTCTTGCAAAAGA[C/G]CTCTTTAAAATGTGT	23077
rs556313530	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77319115	GTTTGGGAACGTGTG[C/T]GTGTGTGTGTTTGTG	23077
rs556317671	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77274482	GAAACATGAAGAGAG[A/G]GAAAGGGAAGGGAGA	23077
rs556336065	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77151751	GACTATCTTTGATCT[A/T]CTAACTCTACTATTT	23077
rs556340017	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77094765	GGAAGCCTTTTCTGA[C/T]TTCCTGGGGAAGATT	23077
rs556369942	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77179324	ATTTGAATGATGTAA[A/G]ATATTTCATATTAGG	23077
rs556373278	in-del	-/TG	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77093926	AATCTATAATTATGC[-/TG]TGTTAGCATTTTTCA	23077
rs556399345	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77158310	TTTCCAGTCTCTTTC[C/T]TCCCTCAAAAATAAA	23077
rs556415376	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77212533	TTTAAAAAGTCACTT[C/T]GACATAGTAAGTTGA	23077
rs556425066	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326812	CGCCGCCTCGTCCCC[C/G]CGGGCCGGGCGGGCA	23077
rs556438683	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77086910	ATCAAATTCATCACT[C/T]CATATTTCTTCTTAC	23077
rs556440020	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77049086	GACCACAACCTACAA[C/T]TTTCATTCAATAATT	23077
rs556441490	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77180694	CTGAGATGGGAGGAT[C/T]ACTTGAGGCCAGGAG	23077
rs556449207	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77088014	GTCTCAAACTCTTGC[A/G]CTCAAGTGATCCTCC	23077
rs556456751	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228278	TGGGAGGCTGAGAAA[A/G]GCAGATTACTTGAGC	23077
rs556501127	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77157773	AAACAAACAAACAAC[C/T]GCCAAACAAAAATAT	23077
rs556509340	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77063420	AAAAATTAGCCAGGT[A/G]TGGTGGTATATGCCT	23077
rs556522114	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77168862	ATTTTTAAAAACTTG[A/T]TTTTTCATGATCTGA	23077
rs556525995	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77057907	CAGTGGTGCCATCTC[A/G]GATCACTGCAAGCTC	23077
rs556541741	snp	C/T	0.000205802	0.0101419	intron-variant	MYCBP2	GRCh38.p7	13:77212195	ATATTAGCAATATTG[C/T]TGTGTAAACAATCTA	23077
rs556542899	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77227195	TATTTTGAATTTTTT[A/T]CTCAAAAAAGATCAC	23077
rs556547529	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77237814	GCTGATCTATTTTTT[A/C]TTACTTATACTCTCT	23077
rs556550892	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77111073	GATATACTACAGGTA[C/T]AGAAGTTTGAGAGAA	23077
rs556558751	snp	C/T			intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075410	ACCTTTCCTACTCAA[C/T]CTTAACTCCTCAGCA	23077
rs556563939	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77289541	TCTAAGTTAGGAATA[G/T]AAGGGAATTTTCTCA	23077
rs556564605	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77317032	TCGGCTCACTGCAAC[C/T]TCCACATCCCAGGTT	23077
rs556568646	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77175788	CAACACAGTGAAACC[C/T]CTCTACTAAAAATAC	23077
rs556572269	in-del	-/ATA	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77172389	AGGTTTGTAGGCCAC[-/ATA]ATGACTTTACATTTT	23077
rs556578479	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77159248	AATAATCTCTCTTAC[A/G]CAGTTAAAAAATTCA	23077
rs556599484	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77051259	GCTCCTTAATTCATA[C/T]TTTGAGGGCCTACAT	23077
rs556604025	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77288083	AAAGCAAAGTATTTT[A/G]GCAATGCGTATATAT	23077
rs556617876	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77213213	GGTGCAGTAGCTCAC[G/T]CCTGTAATCCCAGCA	23077
rs556637134	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77209317	TGTTACGCTTAGTTA[C/T]ACTGTTATTGCTAAC	23077
rs556651815	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77314835	TGGGGGATGTTGATA[C/T]GGATGAGGCTATGCG	23077
rs556665382	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77160993	ATCCTAGGGTCTGAG[C/T]AACACTGATCCAGTT	23077
rs556674888	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77298779	GATTTCCACAAGATA[C/G]TATGCCATAAAAGTA	23077
rs556687689	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77275115	TTCTACACTAGGGTA[C/T]TGGCAAACATGACAA	23077
rs556704604	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77091858	TCCTGGATTTTGATC[C/T]TAAGGGGTAATAGTA	23077
rs556706571	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77214696	TATACAAACCTAGAC[A/G]GTATATCTACTACAT	23077
rs556713388	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77152295	CCCATTCTTATATTT[A/T]AAAAATGGCAGTTTA	23077
rs556714045	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77271733	ACCATGATTGTGAGG[C/T]TTCTCCAGCCATGTG	23077
rs556745790	snp	A/C	0.00914312	0.0669923	intron-variant	MYCBP2	GRCh38.p7	13:77199903	CTGTACATCACCATC[A/C]TCAAAGACCAAAAGT	23077
rs556776508	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77308526	AAAACAGTACCTCTC[A/C]CACTGGATGATGTCA	23077
rs556785056	snp	C/T	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77245309	ACACATGTACATGTA[C/T]GTTTATTTCATCATT	23077
rs556785438	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77251843	CAGTAGGCACAAGAT[A/G]GCTCCTAATTTTCTC	23077
rs556785735	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77144156	GACACACCCACAGGG[G/T]AGAGACAGGGTAACA	23077
rs556821629	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77088682	ATAAACTTTAGAGTC[C/T]GATTTTTATAGGAAC	23077
rs556824336	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77221709	CAACAATAGCCACGA[C/T]GATACAAATAAACCC	23077
rs556824440	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77104781	GACTACAGCAGTTTC[C/T]GAGGATAGGGACTAA	23077
rs556829005	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77266844	CTTTCCAAAGCTCCT[C/T]TATTTCTGAAATGGA	23077
rs556836062	in-del	-/CACACAC	0.00159744	0.0282165	intron-variant	MYCBP2	GRCh38.p7	13:77245746	CAGAACGTAAAGTAA[-/CACACAC]ACACACACACACACA	23077
rs556841697	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77092516	TGCAACCTCTGCCTC[C/T]CAGGTTCAAGTAATT	23077
rs556841732	snp	C/T	1.64969e-05	0.00287196	missense, nc-transcript-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77083090	TCATAAGGTCTGAGA[C/T]GGTCTGCAGCAAGCG	23077
rs556843471	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	MYCBP2	GRCh38.p7	13:77044559	GTTTTGAAAATTATG[A/G]ATGTGTTGTGTTAGT	23077
rs556845588	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77099689	CTTAGAACTCAGAGC[C/G]TGTGTTCCCTTGGAA	23077
rs556849535	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77193610	GAGGACTGATAAAGT[A/G]TAAGTATCCTCTTAC	23077
rs556866899	snp	C/T	6.74821e-05	0.00580831	synonymous-codon	MYCBP2	GRCh38.p7	13:77270518	TACACTTCTCTGTAG[C/T]GAATTTAGAATTGTT	23077
rs556867429	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77137692	CTCCTGAGTTCCAGC[A/G]ATTCTCCCGCTTCAG	23077
rs556880007	in-del	-/G	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77067331	ATATGGTGAGAGGTA[-/G]GTATCTAGAATTTTT	23077
rs556890464	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77219413	CACTAAAGGGAAAAA[A/G]AAAGGAGAGCCAGCA	23077
rs556903973	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77151938	TCAGCAGGTATCACC[A/T]TTCTGAGCTTTACTC	23077
rs556910552	snp	C/G/T			intron-variant	MYCBP2	GRCh38.p7	13:77137570	CCAGCCTGGGCAACA[C/G/T]AGTGAGACCCCATCT	23077
rs556915016	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77299997	TATTCAGTGATATAG[A/G]TCAATAGTTTCTCTA	23077
rs556921403	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77233771	TGTTACCGAGTTTAC[C/T]ACAAATCATAAATAG	23077
rs556930502	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77144681	ATCCTACCACCCTGC[A/C]ATAGTACGCTTGCCT	23077
rs556940555	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77223185	GGATGCACGAGGACA[C/T]TCGTCCCCTGGGGTG	23077
rs556972664	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77148224	TATTTATTTCGGATA[C/T]AGAATTCATAATGAG	23077
rs556975471	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77154480	GAAAAGAAAAAAAGA[C/T]GAAGTCTGACTTTCA	23077
rs556996958	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77224978	GGAATTTAACATTTT[G/T]GTTTTTATAAAGGTT	23077
rs557010608	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77107755	AAATAAATAAATACA[A/T]AAAATTAAAAAAATA	23077
rs557019720	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77115859	TTACATTAAAAAAAG[C/T]CAAACTATAAAAAGA	23077
rs557035214	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77278494	CTGCATTACAGGCTA[C/T]TGTGTGTGCTTCATA	23077
rs557047997	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77172134	TCAAACTCCTGACCT[C/T]GTGATCCACCCATCT	23077
rs557049048	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77316539	CACTATATTTCGCCT[A/G]TTATACAATTAGGAT	23077
rs557049822	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77241091	CAACATAATTTCTTT[A/C]AATATTTAGCTAGTG	23077
rs557054215	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77215167	CATGTAAATGTTCTA[C/T]ATATTTTAAAAATGA	23077
rs557078868	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77224272	TATCTCTACAAAAGC[A/C]CTCAACCATAAGATC	23077
rs557080706	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77234426	TCTAATAAAATTTCA[C/T]AAATGTCAAATTAAA	23077
rs557082081	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77319823	CAGCCAGCCAGCCAA[A/T]AATCCAGCTTCAAAA	23077
rs557083463	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77287327	GTAGCTGGGATTATA[C/G]GCGACTGCCACAATG	23077
rs557086895	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77108983	CAGGCATGAGCCACT[A/G]TGCCCAGCCAGGATA	23077
rs557110135	snp	A/C	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77262861	TAATTTCAATTCAAG[A/C]TTTTTCTAGGGAAGA	23077
rs557183014	snp	C/T	0.0142736	0.0832652	intron-variant	MYCBP2	GRCh38.p7	13:77046942	CAGGATGGGGACACT[C/T]AATGGCAGATCTAGT	23077
rs557184314	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076297	TCCATGTAGATAAAC[A/G]TAAGAGAAAAATGAA	23077
rs557186795	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77240425	CCAGCCTGGCCAACA[C/T]GGTGAAACCTCGCCT	23077
rs557187868	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77147336	ATCTGTTTCTTAATA[A/G]AAAAATAACAAAATG	23077
rs557190780	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77133361	AAACAGAATGATCAT[A/C]TCAAATGCAAAGAAC	23077
rs557192554	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77178121	TAAAACCAGATTTTA[C/T]CATTCTAAATTCACA	23077
rs557218984	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77133753	TGTCCCCATAACTCT[G/T]AACATTTGATTCTCT	23077
rs557224014	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77109739	ATCCTGAATGGAGGG[A/T]CTGGCTGGAACCGTG	23077
rs557226910	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77272759	AGACAGAAAATGACC[A/G]ATATACTCCTTTTGC	23077
rs557267370	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77165709	AAATACTGAGGTTAG[C/T]CTTTTTATTTTTCAA	23077
rs557267570	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77141053	AAATTAACACAAATA[C/T]CTGATTTCTGTCCTT	23077
rs557289081	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77322791	AAGTGCATGGTTATA[C/T]CACCATTCACATTCA	23077
rs557297614	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77301876	GAACCAAGTGGACAT[C/T]CTGAAACTGAAAAAT	23077
rs557302567	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77325567	AGGTGTAGCCAACCC[A/T]AGTAAAAGAGACAAA	23077
rs557304441	in-del	-/AGA	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77195503	TCGGGAAGCTGAGGC[-/AGA]AGAATTGCTTGAACC	23077
rs557324203	snp	C/G	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77284759	ATCATTTACCGAGCA[C/G]TTCTTTCTGCCAGGT	23077
rs557370262	snp	A/C/T	3.54083e-05	0.00420748	intron-variant	MYCBP2	GRCh38.p7	13:77185416	GGTAATTAAGCAAAA[A/C/T]ATTAAATATGCATGA	23077
rs557370519	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77210850	TATGGCACCTAGTAT[A/G]CACCTCTGTAGTATT	23077
rs557384853	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77265500	AAATGACAATTATCA[C/G]ATAAAAAAAGTATGT	23077
rs557385216	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77309533	AGAGAAGAATCCCAA[A/G]AATGGACTCTTGAGA	23077
rs557387456	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77301026	TGTGGGCTGAAATGA[C/T]AGACTGGAATCTAGA	23077
rs557390413	in-del	-/AAAAAACT			intron-variant	MYCBP2	GRCh38.p7	13:77229345	TCCATCTTACAGATG[-/AAAAAACT]AAGGCTTGAAGGGTT	23077
rs557396900	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77208077	TTTTCATGTGCAACA[A/T]GTGGATTCAGTAAGC	23077
rs557404673	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77218280	GACTGGCCTGTTAGA[A/G]ATCTTTATAAATAAT	23077
rs557419931	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77324616	TGATTTCCATGAGTA[C/G]TTCTTGAAATACTTG	23077
rs557440646	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77285758	GCCATTGCACTCCAG[A/C]CTGGACAGCAAGAGC	23077
rs557442616	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77059080	TTTTTTTTTTAAAAA[A/G]GTACCTTTGACTCTC	23077
rs557457695	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77052087	TGCTTGCTGACTGTA[C/T]GTAGGGTGGATCAGG	23077
rs557458006	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77059032	GTATAATTTCCCAGT[C/T]ACCACTCTCCGCATC	23077
rs557464308	snp	A/G			intron-variant, missense	MYCBP2	GRCh38.p7	13:77129175	GGGAAAAAAGCTTTG[A/G]AAGTCCATGAAAATA	23077
rs557467205	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77279218	AGTCAACACAGCACA[C/T]ATAGTAAAAAGATTT	23077
rs557477116	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77124628	ACAAGGGACTCATAA[C/T]TGGGTATGAAGAAAT	23077
rs557492922	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77115574	ATTACCAAATATTCT[A/C]TTTTATGGAATAAAA	23077
rs557497635	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77169366	GCGCCACAGCACTCC[C/T]GCCTGGGTGACAGAA	23077
rs557502993	snp	C/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77159784	TAAACCTCTTTTCTT[C/T]ATAAATTACCCAGCC	23077
rs557537859	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77257040	TAAACACAAGGTAGT[A/G]CTATTTAACCATAAA	23077
rs557570337	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77045817	ACAGAGTAATGAACA[A/G]AAAAGGTCACAAAAC	23077
rs557573742	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77301510	ATCCTAGTAGAGGGA[A/G]GGAGCGGTCTATGTA	23077
rs557579887	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77214176	AATTAAAGGTACCAC[A/C]ACACATTCTGTTGGC	23077
rs557579939	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77264234	CAAGGACCTGAGATC[A/C]CACCTAATTTCAAAA	23077
rs557584390	snp	C/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77316561	AATTAGGATTCACTT[C/G]CTTCAAATAAGGCAT	23077
rs557591750	in-del	-/TTTAGTA	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77108882	CTAATTTTTTGTATT[-/TTTAGTA]GAGACGGGGTTTCAC	23077
rs557614610	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77186343	TTAAAAATAAATTTT[A/T]CAGTGTTCCTGCTAC	23077
rs557656170	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77155977	GAACAAATGGACTCT[C/T]AGCACTTGGCATTTC	23077
rs557658598	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77061102	TTATTCACAGTTTAA[C/T]CAGTTGGCACGGTTT	23077
rs557661675	snp	G/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77149153	TCAAACATCTTGAAA[G/T]GCTTATCTACACTCA	23077
rs557681413	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77201581	CCACCCCAAATCAAC[A/G]GAATATACATTTTTT	23077
rs557705955	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77163767	GTTCTCTCATTTTGC[A/T]AACATATTTCTTATT	23077
rs557710558	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076939	GATTCCGCAGGTTTT[A/G]TAATATGCTACTCTT	23077
rs557711851	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77052700	CTACTGTTTTAATAA[A/G]TATGCTTAGCAGTTC	23077
rs557712257	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77069226	TGAAATTATACATGA[C/T]ATTTTACAATTGAAA	23077
rs557729398	snp	C/T	3.33139e-05	0.00408116	intron-variant	MYCBP2	GRCh38.p7	13:77263835	ATTACATAAAGAGGT[C/T]GTTCAAGGCTCTACA	23077
rs557736583	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77108633	ATCCTGAGAAAGAGA[A/C]AACGCTTACGCAGCA	23077
rs557745349	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77052229	TTTGAGACGGGCTCT[C/T]ACTCTGTTGCCCAGG	23077
rs557763604	in-del	-/C	0.00149365	0.0272873	intron-variant	MYCBP2	GRCh38.p7	13:77099204	CACATCATTACACAA[-/C]CATTACCACCAAAAA	23077
rs557763906	snp	A/G	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77315663	ACTTTCAGAGTCTGA[A/G]GCAGGTGGATCACCT	23077
rs557768400	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77125611	TTCTGAAATTAAGGC[C/T]ACAGCCTGAGGTAAG	23077
rs557777891	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77187248	TCACTAAAGAAAGCA[G/T]AACAGAGTCAAAGAT	23077
rs557783349	snp	C/G	4.97979e-05	0.00498964	missense	MYCBP2	GRCh38.p7	13:77095401	GCATTTTCACAGGAA[C/G]ATCCTCAGAAATGCC	23077
rs557807993	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77216107	CTGGAAAGAAAGGAA[A/G]CACTCCAAAAAATGA	23077
rs557815468	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77312706	AAAAAAAGAGAAACA[A/G]AAGACAATAAAGTGG	23077
rs557822959	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77218371	AAATAATTTTATGAT[C/G]ATCTTTTCTAACTTT	23077
rs557827071	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326410	ACACACGCGGGTGCA[C/T]GCGCGGCATGGGGCG	23077
rs557828329	in-del	-/AAGAG			intron-variant	MYCBP2	GRCh38.p7	13:77235336	GACAAAAAGTTTAAC[-/AAGAG]AAAAGGAAAGGAAGA	23077
rs557839410	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77325683	TTCCCTACAAAACCC[C/T]CTCTACTCTAAAGCC	23077
rs557841579	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77256361	TCAAAGATGCTAAGC[C/T]AAAGAAGCACTATTT	23077
rs557849268	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77069567	ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA	23077
rs557888679	in-del	-/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228691	CCTAAGATGAATATG[-/T]TGTGTGTGTGTGTGT	23077
rs557933895	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77210925	AGTAACTTCTCCAGG[G/T]TGACACAGAAAGCAA	23077
rs557965462	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77249298	TCATAATAAGATATG[C/T]AGTCACAATTTTATA	23077
rs557973445	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77141197	ACTAGAACATATGAA[A/G]TGATACAGAAAAAAT	23077
rs557984955	snp	A/C	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77315362	AGAAAAGAAAAAAAA[A/C]CGATTACAGACCAAT	23077
rs557989530	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77234490	GTAAAGGAACCATAT[C/T]TCAATTATGTTTCTA	23077
rs557999314	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77250914	TCTGTTTTTAAATAA[C/T]GGTTTAAATGAATCA	23077
rs558000578	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77225823	ACCTTATGTAATAAA[C/T]GGGTCATTAAGTTAT	23077
rs558008588	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77100348	GTCAAGGGCAGGTAT[G/T]TTTGTCTGTTACTCT	23077
rs558019530	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77307592	GGTCATGCCACTGCA[A/C]CCCAGCCTGGATGAC	23077
rs558019635	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77278619	ATGTGGACTAATTAA[A/C]ATCTATCACCTCAAG	23077
rs558029597	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77102994	TGTTTAACCTATAGA[C/T]GTAATAAACATGCAT	23077
rs558041388	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77242148	GAGATGGAGTCTCAC[C/T]CTGTCGCCAGGCTGG	23077
rs558049646	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77133860	CACAACTTATCACAA[C/T]GCAATTTAATTATGT	23077
rs558058669	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77303789	AAAAAAAACACTGAA[A/G]GTAAATTATCTAGAC	23077
rs558063002	snp	G/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77266336	CCTGGAAGGCTTTCA[G/T]TCTCAAACATTAATC	23077
rs558102011	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77318320	TTTCCATGCACTCAT[A/G]GGCCAAAAGAAATAC	23077
rs558113456	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77229569	TAATTCAATTCAAAA[C/T]ATTAAAGCTAGTATT	23077
rs558143541	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77279787	TACTAGACCCTGTCC[C/T]CTAAGAGTTTATAAT	23077
rs558165033	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77203133	GACGACATGATTGTA[C/T]ATCTAGAAAACCCCA	23077
rs558173057	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77079913	TAGATGTCAGCTTAC[A/G]TGTTGGGAATTTTGA	23077
rs558180034	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77224712	CTGAAAAATATTTTT[A/G]TAGGTCATATAAATG	23077
rs558180048	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77178206	CCACTTAATTTATAA[A/T]GTCAGAAGTACAAGC	23077
rs558186637	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77134758	ATGTTATTTTGTCTC[C/T]CAACTAGAGCATTAC	23077
rs558187179	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77221660	CCTTTCCCAGTTTCT[A/G]TGGCTCACAAAATAA	23077
rs558187817	snp	C/T	0.0158469	0.0875917	intron-variant	MYCBP2	GRCh38.p7	13:77310777	ACACAGACGTGTGTG[C/T]GTGCGCATGCACACA	23077
rs558229790	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77279270	GCCTTTTCTATAATG[C/G]TACAATCACTATATT	23077
rs558244343	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77072958	ATCTTGTTTACCTCT[C/T]TCATCATTTATTTTT	23077
rs558247613	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77060551	TCAACATAACTTTGA[A/T]CTAGGAATATACAAG	23077
rs558270033	snp	A/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77116464	AATTCTGAATTATTT[A/T]AAAAAATTAAAACTA	23077
rs558277879	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77129463	TAGTGTGTCATGCCA[A/T]TTACTAAAATTAAGA	23077
rs558278336	snp	C/T			synonymous-codon, utr-variant-5-prime	MYCBP2	GRCh38.p7	13:77225460	AAATCCACAGCTGAC[C/T]TGGACTGCCCGGAGC	23077
rs558281386	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77106355	TACTATGTTCTATAA[C/T]CAAGCTGTGACATTC	23077
rs558294307	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77110275	GGGAGGTCTATAAAC[A/G]GCTGCTCTGGGAGTG	23077
rs558296778	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77202278	CTCTACGCAAATAAA[C/G]TAGAAAATCTAGAAG	23077
rs558303318	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77272835	GCCCTAGGGTTGCCC[A/G]AGGGGCCAGAGAAGA	23077
rs558321690	snp	A/C	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77125960	ACCTATGAATGGGAA[A/C]AAAGAAATGAAACCT	23077
rs558331618	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77257930	ATTTCTGGGGCAAAA[C/T]AACTCAACAAAATGA	23077
rs558338989	in-del	-/AGAC	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77138763	AAGAGAGTCAAAATT[-/AGAC]AGAACACACAGAACT	23077
rs558360189	snp	G/T	0.000399281	0.0141238	missense	MYCBP2	GRCh38.p7	13:77164511	AAACCCCACCAAGAT[G/T]GGCTAATTCTTTTTC	23077
rs558401065	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77063933	CCTAGGGATATATAG[C/T]TTATCTTCTTCAGAT	23077
rs558402367	snp	C/T	0.00438332	0.0466095	intron-variant	MYCBP2	GRCh38.p7	13:77254564	ACATGCATATAATGT[C/T]TAATGATCAAATCTG	23077
rs558417094	snp	A/G	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77290372	TTGGACATTTACACC[A/G]GAGAAATAAAAACTT	23077
rs558419078	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77106825	GTGTCATGGGGGTTT[C/G]GTGTAAACATAATTT	23077
rs558422612	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77273417	TGACAGAAATTGAGA[C/T]GAAACTGTAACTTGT	23077
rs558423052	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77047391	TTAAGTATCCTGGCA[C/T]GAGAAGGTAGTCAAT	23077
rs558425791	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77094299	CTTTTGGAGTGTCAG[C/T]GCATGATGTGTGAAA	23077
rs558440212	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77150427	GATTATAGGTGTGGG[C/T]CACTGTTCCTGGTCA	23077
rs558448320	snp	C/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77303316	CCAGCCTGGGCGACA[C/G]AGCGAGACTCCGTCT	23077
rs558451962	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77319597	TTCTCCAATCTATCA[A/C]TGTTATTTACCAAAA	23077
rs558458450	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77054382	AGTAGAAGAGTGATC[C/T]AGTTAGATTTTAGAT	23077
rs558493498	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77214078	ACTAAATATGGATCC[A/G]AACTTTGAGGATCAG	23077
rs558502843	snp	A/G			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77079591	CTCTGTGGTAGGCAG[A/G]TTGAGGAACATGGAG	23077
rs558506892	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77238137	AGTCCCAGCTACTCG[A/G]GAGGCTGAGGCAGAA	23077
rs558511006	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77246427	GAGGTCAGGATTACC[A/C]CAATACCAATGTCAG	23077
rs558511344	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77255340	CTGCTTTCTAATTCA[A/T]TACTTACCAGCAGGG	23077
rs558521169	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77153464	GTCTCAAACATATTT[A/G]ATATTAAATTACAGA	23077
rs558537795	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77248324	TCAACAGAGTAAAAA[C/G]ACAACCCACAGACAG	23077
rs558544380	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77091118	TGAAATCCTGTGTCC[C/T]TTGGTAAAATTATCT	23077
rs558550067	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77275502	CCTCTAAATCTCATA[C/T]GTCACATCTTCAGGG	23077
rs558571514	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77290322	TTCCTACAAAACTAA[A/G]TATGTGCTTACCATA	23077
rs558572981	snp	C/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77065620	AAGAAGAATAAAGGG[C/T]TTAAAAACCATGAGG	23077
rs558591743	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77130794	TCACTTTTTTTTAGC[A/G]TATTCTATTTTTTAG	23077
rs558597327	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77138364	ACATTATTATGGACA[A/G]TCAAGGAGAAAGTCA	23077
rs558606893	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77121284	TTAATAAAGATTTCT[G/T]GGTGAACACAAATAA	23077
rs558610160	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77284279	GAAACCTCAGGCAAG[A/C]AGGAATGGGACAGCC	23077
rs558611321	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77207221	CTCAATGTATAAGAG[C/G]TAGAAACAATCAATC	23077
rs558631523	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77264213	TATTTATAAATCTTC[C/T]ATAACCAAGGACCTG	23077
rs558634220	snp	A/G	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77282412	TGAAACTCCATCTTG[A/G]AAAAAAAAAAAAAAA	23077
rs558634303	snp	C/T			missense	MYCBP2	GRCh38.p7	13:77205337	GTCGGCACTGAAACG[C/T]ATAGCTTCTACTGAA	23077
rs558638581	snp	A/G	0.00279162	0.0372561	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77083556	GTAGGTATGTTTTGT[A/G]TGTATGTTTATGTAT	23077
rs558653470	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77139427	AAAGCAGAAAAATGA[C/T]GGTGCATGTGCAGAT	23077
rs558666079	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77130056	AATGTTTTACTGATA[A/T]TTTAAATGATATACA	23077
rs558706632	snp	A/C	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77056696	TGTCAACTGAGCTCT[A/C]TAGTGGTCTGAGAGT	23077
rs558710109	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77275994	GTCTCAAAAAACAAA[A/C]AAGGACTCTCAGAAC	23077
rs558710447	snp	C/G	0.0178098	0.0926698	intron-variant	MYCBP2	GRCh38.p7	13:77052248	CTGTTGCCCAGGCTG[C/G]AGCATAGTGGCGCAA	23077
rs558714764	snp	A/T	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77269606	ACTCTAACCTGGGTG[A/T]CACAGCGAGATTCTG	23077
rs558744847	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77232871	AGAAAGCAATAATTA[A/T]TTTTTCCACCTTCCC	23077
rs558765133	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77167846	GCTTGTTTACTTCTA[C/T]ATGCTTAATAGTTTC	23077
rs558769798	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77153560	TTAATAAATTATCAT[A/T]AGAGTCTATGTGTGT	23077
rs558784399	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77091674	CAACAGAGAGGCAAA[C/T]ATCACCCTCAATTGA	23077
rs558800056	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77276216	TATATTTTTAAATAG[A/G]TAATTTAAAAATCAA	23077
rs558812178	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77177452	GCTCAAGTGATCCTC[C/T]CACCCCAGCCTCCAG	23077
rs558828681	snp	C/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77166957	AGATGGGATATACTT[C/T]AAAGACAAAACACAC	23077
rs558828791	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77168966	CTATTTTAAAACACT[C/T]TTATCCTTTAACATT	23077
rs558842998	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77306869	ATATAGACTTCAGAT[A/G]GTGGGATTTTCGGAA	23077
rs558844648	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77285515	CTATTGGCCAGGCAC[A/G]GTGACTCACACCTGT	23077
rs558845205	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77214496	ATATGGAGTGATTTC[C/T]AGGAGAGATGCTGAA	23077
rs558845798	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77278380	TGAGAAATGTGTGTG[C/T]ACGAACTTCAACTCT	23077
rs558855080	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77050649	ACGGTTCCAGGCTTC[A/G]TTAAAAAAAAAAAAA	23077
rs558863858	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77271586	ATGGGGGCAAGTCTT[C/T]CCTGTGCTGTTCTCA	23077
rs558903667	snp	A/C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77069846	GCACTCCAGCCTGGG[A/C/G]AACAGAGCGAGACTC	23077
rs558935826	snp	C/G	0.00438332	0.0466095	intron-variant	MYCBP2	GRCh38.p7	13:77213606	TGTATTCCCTTACTA[C/G]CAACTAATATGAAGA	23077
rs558936792	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77068077	GGATTACAGGCATAA[A/G]TCACTGTACCCCATC	23077
rs558940167	snp	A/G			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228219	AGCAAGATTAATTCT[A/G]CTCAAGCTGGGCATG	23077
rs558951224	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77149124	AATTCCATTTCCTCT[C/G]GTTCTTTCTATAGTC	23077
rs558966162	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77239434	ACAATCTTTTCTAGC[A/C]CAGTGCCAGAGAAGA	23077
rs558967186	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77064843	ATATTTGTTTTTAGT[A/G]AGACCATGGAATTTT	23077
rs558989599	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77322371	TCAGGACCCAGATAC[C/T]CTGACTCCTCTTTAT	23077
rs558993051	in-del	-/AA	0.00478085	0.0486577	intron-variant	MYCBP2	GRCh38.p7	13:77239342	ACAGGCCAAAGAAAT[-/AA]AAGATCTGTATGTAT	23077
rs558993272	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291795	AAAGCTAAACTAAAC[G/T]TACATTTACCGTGCC	23077
rs559002979	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77199298	CGGCACCTGGAAAAT[C/T]GGGTCACTCCCACCT	23077
rs559009739	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77177177	AACTACTCAAGACTT[G/T]TCATCAGGGACTTAG	23077
rs559011924	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77270601	CAAACACAGAACAAA[C/G]ATACTTTGGTAATAC	23077
rs559030843	snp	A/G	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77233427	CCCCCACCCCCACCC[A/G]TAACCTAATCACCAT	23077
rs559034534	snp	A/C	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77307635	TGTCTCAAAAAAAAA[A/C]AAAAAAAAAAAAAAA	23077
rs559039071	snp	G/T	0.000102847	0.00717029	intron-variant	MYCBP2	GRCh38.p7	13:77260621	ATTAGATTAAATCAA[G/T]ACCTCTATGTACAAA	23077
rs559048286	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77206578	AGAATTACATATAAA[A/T]TTAAATACTCTAAAA	23077
rs559064239	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77066116	TTAGCACTTAAAAAG[A/C]CAATAAATTATCAGT	23077
rs559080207	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77089844	AACATTTGGCTTAGA[C/T]ACCTAACAAGTAAGA	23077
rs559080789	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77193238	GCTTTCTTAAAATTT[C/T]CCCTAATATTCATTT	23077
rs559098246	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77118905	TACCACCCTGCCTCA[G/T]CGGCAGTATATTTCA	23077
rs559104475	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77119302	TGGAGGTGGGGAGAG[C/G]GAACTACATCCAGAC	23077
rs559111061	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77245827	AAGGAAAAAATAATA[C/T]ATATATATGTATATA	23077
rs559115086	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77099439	AGCAGAGTGATACCT[C/T]GCATCCTTAGGGCAA	23077
rs559122251	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77295897	AGGCTCAGAACAATA[C/T]GGACACACCAAGTTT	23077
rs559131442	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77055397	CAAACAAGTTAAGTA[A/T]ACAAGTTTTACTGGA	23077
rs559133225	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77151746	AACGGGACTATCTTT[A/G]ATCTACTAACTCTAC	23077
rs559151150	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77284623	CACTGATTCTCTAGA[A/C]GTTTCATTTGCTTGC	23077
rs559152008	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77130354	TTCTCATTATCTCAT[G/T]TTAGATAATGAGACT	23077
rs559152243	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77096537	GTCCTTAATAGTTTG[A/T]TCCTTATTACTCATA	23077
rs559157218	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77058588	TAGGCTTCTTAACAA[A/C]GTTTTTTTTTTTTGA	23077
rs559158153	snp	A/G			upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77327753	CTCACTCACCTAAGA[A/G]TGCACTTTTATCTCT	23077
rs559176133	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075070	AAAATCAGCTGGGCA[C/T]GGTGACGTGCACCTG	23077
rs559189412	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77127323	CTAAAATGAAAGAAC[C/T]TTCCCTAAATTTTCT	23077
rs559193021	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77323185	AAGTTATGTAATATA[C/T]TCAAAGTTACACAGC	23077
rs559193189	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77130434	GGATATATACATATA[A/T]ATGTACAGATGAATG	23077
rs559197379	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77239020	AGCTACTCGGGAGGC[C/T]GAGGCAGGAGAATCG	23077
rs559198176	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77253203	AGAGATGTTCAAACT[C/G]AGTATTAATAATCAA	23077
rs559208310	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77279843	TATAATTCATACTCA[A/G]TACAGACCTCTGTTA	23077
rs559219669	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77067100	GTCAAATCTATAAAT[A/T]TCTTCCTATATGATT	23077
rs559222731	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77238638	TTAATACCTAAAAAG[A/G]TAAATTAAAAAAATT	23077
rs559251832	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77223973	CTACTACTATTTGCA[A/G]TAAGTCAAAAGAGTT	23077
rs559252175	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77251928	TCAGGGCCTTTGTTC[A/C]TTCTTGCTCCCTCTG	23077
rs559253462	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77215379	AGAGCAAGAATGACC[A/T]TTCAGTGAGTTTGTT	23077
rs559258029	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77178781	TCCCAAAGTTGTATA[C/T]CAGGCACCCTGTAAC	23077
rs559294138	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77208701	CTTCATACTTGTGAT[C/T]CACAGAGAAGGCTAG	23077
rs559295964	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77176152	TCAATACTACTACAA[C/T]GCAGGTATTATTCTT	23077
rs559305259	snp	C/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77112217	TCTTGCTTGTTATGA[C/T]GGATAACTATTTATG	23077
rs559313885	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77130975	TCTCAGTCAACAACA[A/T]GTACAATGATATTTT	23077
rs559330125	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77122033	TATTTTTCCCAAATA[C/G]AAGGATAATAATAAA	23077
rs559331654	snp	C/T	0.00755907	0.0610114	intron-variant	MYCBP2	GRCh38.p7	13:77295557	TTCTCTCAGTTACAA[C/T]AGTAAAAACACTAAC	23077
rs559337071	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77223512	ATTCTGACTGCATTA[C/T]GTAGAATACAAACTC	23077
rs559338426	snp	A/C	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77139522	GAGTGCCAACACAAT[A/C]TGGTAATTCATGTGG	23077
rs559344805	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77269003	TTCACTGTTCAGGTA[C/G]GTACTGTATGGAAAA	23077
rs559362625	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77192264	TGCTAGCAGGGCAAC[A/G]CAGGGCAAGTTACTC	23077
rs559377727	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77283679	AGGCGGTCAGACTGC[C/T]TGAGCTCAAGAGTTC	23077
rs559378678	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77159595	TGAATCATGGGGGCA[A/G]ACTTCCCCCTTGCTG	23077
rs559397695	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77306519	AAGCTACCTTGGCAA[C/T]GGGCAGAGCAGCAGA	23077
rs559402368	snp	A/C	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77269862	CTACACTATTCAGTT[A/C]TTATGGCCATATTAG	23077
rs559435418	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77159499	TGAACTCTGATATGG[A/T]TTGGCTCTGTGTCCC	23077
rs559451243	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77122827	TAATCTATCCCTTTA[C/G]CAGCATTTGTAGACT	23077
rs559457859	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77074030	TTTTTTTTAAAGAAA[C/T]GGTCAAGCTGATTCT	23077
rs559459680	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77311325	AGAGTTTACAAAACA[C/T]AACATTAACCATGTC	23077
rs559467180	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77191337	ACTATCAAATTTAAT[A/G]TCACATATCTACTTC	23077
rs559471977	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77263316	TCAAATTTTTAAATA[A/G]TTGAAAAATGATGCA	23077
rs559491576	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77061403	AATGGCTTTCATTTA[A/G]GCACTCTAAGAAGTT	23077
rs559504305	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77198960	TGAAAATAATTTTCC[C/T]TTCATTTCTTCCCTT	23077
rs559513562	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77152656	TAACCTCAGATGGCA[C/G]CACTTAGGAGAGGAG	23077
rs559513874	snp	A/G	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77160089	TTTTTTTTTTGAGAC[A/G]GCGTTTCACTCTTGT	23077
rs559533677	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77066367	CACGACTTATTTCTA[A/G]GGCACATGCGGATAA	23077
rs559537979	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77223561	CAAGTAAGAGGGACT[G/T]CAAGATACAAGTTTA	23077
rs559559641	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77262208	CACTATTTTAAGTGA[C/T]TGCAATGTCAATTCA	23077
rs559563320	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77270719	AAATCTCAAGCAAGG[C/T]AGACTTCCTTACTCT	23077
rs559580609	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77268739	AGCTGAGATCACGCC[A/G]CTGCATTCCAGCCTC	23077
rs559588479	snp	A/G	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77302816	TATTAAAAGAAATGA[A/G]AAGAGCATTTCTAAA	23077
rs559592817	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081250	ATGGAATTCCACAGT[C/G]CTCCCAATCATATTA	23077
rs559595626	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77134337	GAGTTCGAGAGCAGC[C/T]TGGCCAACATGGTAA	23077
rs559622202	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77298681	CATCTCTAGCCAGAA[A/C]GGCCCACTAAGGAGT	23077
rs559632977	snp	A/G	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77138741	ATAGTATTATAAGCC[A/G]AGAAGGAAGAGAGTC	23077
rs559642624	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77191345	ATTTAATATCACATA[A/T]CTACTTCTTTTTTAT	23077
rs559644658	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77154593	AAGAAATATCAGAAG[C/T]GTAACAGTATGAACA	23077
rs559667553	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77277237	CAAATCCAAGAAAAC[C/T]GAGCAAAATATTGTT	23077
rs559677171	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77161800	AATGAATAAAGTGAA[G/T]TACTTAATGAATGAA	23077
rs559705044	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77299326	TCTTTCTATGCATGA[C/T]GGCATTTAATTGGTT	23077
rs559752559	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77262400	TAAAAATTCAATGTC[A/G]GCAATATTCCTTGAA	23077
rs559767108	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77114156	TACATTAAGAATCTT[A/T]AAATAGGTAACTGAA	23077
rs559776862	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77073423	CCCCCAAAAAATCTA[C/T]AGTTCACATCACACT	23077
rs559794495	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77273120	TTCAATAGAGAAAAG[A/T]TATTTAAAACCATGA	23077
rs559813261	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77107241	ATAGGTCTAACTTTA[C/T]AGTTGAGGATATTTG	23077
rs559816155	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77051474	AAATTAATGAAATTA[A/G]CCTCTCTTATAATCT	23077
rs559821608	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77073457	TAATGAATGGTTTAT[A/G]CTTTCTTTTCAAGAT	23077
rs559825416	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77183844	TGAGCCACCGTGCCC[A/G]GTGAACCCCTATTTC	23077
rs559836259	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77222688	CTCTCAGAAATGCTG[A/G]ATGTAGAATCCACAT	23077
rs559840601	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77107989	GTATACTAAAAGAAT[C/T]AGACTAAAGATTTGT	23077
rs559845283	snp	C/T	3.3699e-05	0.00410467	intron-variant	MYCBP2	GRCh38.p7	13:77126297	GTATCTTAGAAGTCA[C/T]GAAGCTACAAGAATC	23077
rs559852063	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77104730	CTGACACCTTAGAAC[C/T]GACAACTGAATTTGG	23077
rs559855457	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77324089	AATCCCCTTGAGTTA[C/G]CAAAAACACATTCCA	23077
rs559868530	snp	C/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77322600	GTAACATTTCATGGG[C/G]ACTTACCAGGTGCGG	23077
rs559878198	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77164799	TCCTTGGTTTTATCT[C/T]ATTGTATGATTTAAA	23077
rs559885479	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77304526	TAGGAGTAAGTTTGA[A/G]TGTTATATAGCACCA	23077
rs559897778	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77309612	TGCACTTGAGATCTA[A/G]TCACCTGCTAAATAT	23077
rs559904074	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77107212	CAGCAATAGGCTCCT[A/G]CAAGAAACAGTAAAT	23077
rs559958342	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77117883	GATCAATTTAACATA[C/T]TAGGAACAACAACAA	23077
rs559959908	snp	C/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77047759	TAGTCAGGGGGCTCT[C/G]TCCTTTTGTGGGCAT	23077
rs559964137	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77164229	CTGGCTCAAAGCATG[C/T]ATATGCATAAAAAGG	23077
rs559987071	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77199953	GGGAAAAAACAGAGC[A/G]GAAAAACTGGAAACT	23077
rs560002980	snp	C/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77171158	GTTTTGGGTGGATAG[C/T]GATACATTACTGGAA	23077
rs560005178	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77308085	AGTTACTGAACATCA[C/T]TAGACTGCTGGTCTA	23077
rs560007645	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77255772	ACAAAGAATGGTGGG[C/T]TTCTGAGATCCAGAT	23077
rs560010523	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77303561	GAAATTAAAAAAAAA[A/C]AAACAACTAAGAAAT	23077
rs560017525	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77157811	CATTTTATATTTCAG[C/T]AAGTTAAACATACAT	23077
rs560034299	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77058072	GTCTCGATCTCCTGA[A/C]CTCGTGATCCACCTG	23077
rs560067801	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77296457	ATGAAACTAAAAGAG[A/G]AACCAAATCATAAAG	23077
rs560078879	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77188351	CAAAAACATCTTACA[C/T]CCCTTATCTCATTAG	23077
rs560092731	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77151858	TTGTTTATGCATTGG[C/G]AGAAAAACACTTGAC	23077
rs560098430	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77110097	ACAAGGGAAGACAAC[C/T]ATAAGGTCTGACTGC	23077
rs560115826	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77209399	TTTGCTAATGCAAAT[A/T]TACTTCATTTAAAAA	23077
rs560132688	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77178539	TTGAATACGTACACA[C/T]ACACATGTGCAACTA	23077
rs560133948	snp	A/T	4.94931e-05	0.00497434	synonymous-codon	MYCBP2	GRCh38.p7	13:77098637	TGAGGAGGAGCGTGG[A/T]GAACTAGCACCCGAT	23077
rs560162668	snp	A/G	8.2659e-05	0.00642827	missense, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77077365	CTTGTTACCCAGCCA[A/G]TGTGCCTGGAATCCA	23077
rs560162756	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77069415	ATCATGAGATCAGGA[A/G]ATCGAGACCATCCTG	23077
rs560175985	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77280717	TGTAATAACAAGTGA[A/G]TGGCAATAGGCAACT	23077
rs560180143	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77317837	AGCAACTCAGGAGGC[C/T]GAGGTAGGAGAACTG	23077
rs560181528	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77203942	TAAAACCATAAAAAC[C/T]CTAGAAGAAAACCTA	23077
rs560189382	snp	A/C	5.18973e-05	0.00509372	intron-variant	MYCBP2	GRCh38.p7	13:77189082	ATAAAATTATGTTAG[A/C]AAGTCCAATGTCATT	23077
rs560194129	snp	C/T	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77311188	TTCTGGCCAGAGGAA[C/T]TGAGAAAAGAAACTG	23077
rs560210539	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77258888	GGTAGAAAAAAACAA[A/G]AAGAAAACTCTTAAA	23077
rs560216021	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77119995	CAATGTTTGTGTCTC[A/G]AACATTTATATTTAT	23077
rs560224103	snp	A/G	1.69163e-05	0.00290824	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076745	CTTTAGAATACAAAT[A/G]AATACATTGTATACT	23077
rs560233963	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77296844	TACTAACATATAAAG[C/T]AGCTATTGAGAAGAT	23077
rs560247029	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77179093	TATGCGAATTTCTTA[C/T]GTATGAATTTCATAC	23077
rs560250523	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087400	TAGATCTGCGAATGA[C/T]TTCATGCAAATTATT	23077
rs560264899	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77143788	ATATGGTACAGCCTA[C/T]TGGTCTTAGGCTACA	23077
rs560272404	snp	A/C/T	0.00119737	0.0244387	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77327551	TGTCATTAGGATTTA[A/C/T]GCTTGTTTAACACAG	23077
rs560275433	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77062505	AACTGTTTATGTTGA[C/T]GTGTTTTTTGTTTGT	23077
rs560276178	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326901	GGCTCCCGCAGCAGG[C/G]AGACTACAAAGACAG	23077
rs560283261	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77071776	AGCAGAGTTCACATT[G/T]TTTTGAAGTGCACGT	23077
rs560286727	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77197231	GTAGGAATGGTAAGA[A/G]AGAGAATGGAGACAG	23077
rs560298511	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77069855	CCTGGGCAACAGAGC[A/G]AGACTCCCTCTCGAA	23077
rs560336345	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77265931	ATGGGACTATCTTCC[C/T]GAAGTTTGGTTCATT	23077
rs560344705	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77171939	AGAGTCTTGCTCTGT[C/T]GCCCAGGCTGGAGTG	23077
rs560374964	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77288807	GATATAGAAGTTTAC[A/C]CAGAAATGAGGGCCT	23077
rs560400314	snp	A/G	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77320294	CATGTGCCTGAAAGC[A/G]GGATCTGAAAGCCTA	23077
rs560405752	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77092649	CAGGCTGGTCTCAAA[C/T]TCCTGACCTCAGGTG	23077
rs560422622	snp	A/G	0.0103295	0.0711199	intron-variant	MYCBP2	GRCh38.p7	13:77072329	AAAAGAAATCAAATG[A/G]GAATAAGAAAACTAA	23077
rs560422861	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77063849	GGTAGGAAAGGATTA[A/C]TGTCAAAAATACCTA	23077
rs560432297	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77172789	TGTCTACTAGCCAAC[C/T]ATAACGAACATCCTT	23077
rs560444829	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77110722	TCCTCTTTGTACTCT[A/T]TCTCTTTTTTTCTCA	23077
rs560451317	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77220636	ATTCTCCAACTGTAA[A/C]CCTTTATTTCAACTA	23077
rs560457180	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228830	AATTATATACACATA[C/T]TTGTATACACAGAGA	23077
rs560491270	snp	C/T			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075964	GACAAGGGAAATCCT[C/T]GAAATTTATCTTTCA	23077
rs560533030	snp	A/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77227683	AATTAAACATTTCAA[A/G]TATCATTCCACTTTA	23077
rs560536197	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77251790	CAAACCTCCAGTGAC[C/T]TTCCAAGGTCTTCAG	23077
rs560544435	snp	A/G	0.000132615	0.00814186	intron-variant	MYCBP2	GRCh38.p7	13:77205448	CAGTTGTAAGACAAC[A/G]TTTCCTAAACCGAAG	23077
rs560570615	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77259338	CTTCCCCAATATTTA[A/G]GTTCTGTAATACCCA	23077
rs560574138	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77155588	CAATATGGTATACAA[C/G]TATTTCAATTCCTCA	23077
rs560582123	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77213407	TTGAATCTGGGAGCC[A/G]GAGGTTTCAGTGAGC	23077
rs560586224	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77136116	GAGCCACCGTGCCCA[A/G]CCTGTTTTTATCTTT	23077
rs560591204	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77135634	TTAGAGCCCTATGCC[A/G]ATTAATTTTGCCATA	23077
rs560621333	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77272146	TGTATGCTGTGGCTA[C/T]GCTATTTGACAGCTC	23077
rs560633140	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77165822	AGAAGAAGTTTCTGA[A/C]ATGAAATTGCCTATT	23077
rs560637903	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77274890	CTTCCTCTCTTCACT[C/T]GTCTGTACACATCCT	23077
rs560659859	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77128911	CACTAATCTTAGATA[C/T]AGTCATTGGAAAAGC	23077
rs560689182	snp	A/C	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326955	TTCTCCTCCTCCCCC[A/C]CGCGCCGCCCTCGCC	23077
rs560721877	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77280957	CAACAAAAATCAACC[A/T]CAAGTTCTGCAACTA	23077
rs560733539	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77120616	GTTACCTGTGGACAA[C/T]AGGGCTGATTTTGAA	23077
rs560755937	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77241903	ATTTCATGCATCAAA[C/T]ATCATGCCATTTCTA	23077
rs560757375	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77069884	AAAAAAAAAAAAGTT[A/T]GAATAATAGGTTAAT	23077
rs560765578	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77166935	CACAGTAATTTGACA[C/T]ACACTTAGATGGGAT	23077
rs560767401	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77162172	CAAGGCAATACTCAA[G/T]AAGCATCCATGGGTG	23077
rs560768667	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77111381	CTTTCAAAACAGAGC[A/C]TAAAAGTAGATGTCA	23077
rs560769532	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77079326	CTTACAGATTTGAAG[A/T]AGGATATATGAGAGG	23077
rs560787193	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77267591	CAGCAGTGGTGGGGT[A/G]AGGTCAGAGATTAGG	23077
rs560791245	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77258937	CCAGTTAAAGATTAA[A/G]TAAACTGTTACCCAA	23077
rs560800177	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77110760	CAATGCTTAGGGAAA[A/G]TAGAAAGAACCTACG	23077
rs560822074	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77171979	GATCTCGGCTCACTG[C/T]AACCTCCGCCTCCCA	23077
rs560842375	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77061877	TTTATTTACAAAAAT[A/C]AACCGTTATTCGGAA	23077
rs560867874	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77151924	ACCACTTTAGTTCTT[C/T]AGCAGGTATCACCAT	23077
rs560868683	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77219383	GAATACACAAAGTAG[C/T]TCTAAGTATCCCAGC	23077
rs560877750	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77269429	TCACTTCAGGTCAGG[C/G]GTTTGAGACCAACCT	23077
rs560900691	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77235399	TATAAATTAGGATTT[G/T]ATAAAAGCATAAAGA	23077
rs560912204	snp	C/T	1.64768e-05	0.00287021	synonymous-codon	MYCBP2	GRCh38.p7	13:77070637	TTAACCAACCTGTTT[C/T]TGTAAGTTAGTCAGC	23077
rs560941316	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77144926	TAGTCCCTCCCCTTG[G/T]GCTGTGAATCTTATT	23077
rs560944652	in-del	-/AACACA			intron-variant	MYCBP2	GRCh38.p7	13:77229662	TTTAATCTTCATAGC[-/AACACA]ATCAGTTAAGAATTA	23077
rs560954826	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77319257	GGGGTAAGAGGGACA[C/G]CACAGTCTGCAAGCA	23077
rs560954930	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77311434	ATGCCAACCCTAAGA[C/T]GATGCACATGTTGTA	23077
rs560958114	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77288900	AGTAAACTGTAGATG[C/G]TTCCCTAAGCTCTCT	23077
rs560976742	in-del	-/T			intron-variant	MYCBP2	GRCh38.p7	13:77070406	TAAAGTATTAGGAGA[-/T]TTTTTTTTCTTGCAA	23077
rs560977433	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77062849	TCCTGATGTGGTAGC[A/G]GGCATACACGATCAC	23077
rs560981131	snp	A/C			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77227417	CTCAGTTCAAAGCCT[A/C]CTCATGTTGGAAAGA	23077
rs561025957	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77272403	ATTCCTAAGTCTCTA[C/T]ATAAAAGCAAATCAT	23077
rs561040443	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77304267	AAAGAAAATGTGATA[C/T]ATATACACAATGAAA	23077
rs561043056	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77327287	AGAGTAAGGAAAGTG[C/T]TGGGGAGGCTGTCAG	23077
rs561046040	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77262565	AGGTTAGTCCAGACA[A/C]AGAGTCATTCAAGCT	23077
rs561049424	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77055069	AGGTCACCCAAGGTA[A/C]GGAAGTATTTATTAA	23077
rs561056688	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77129397	AGTAAACAACACACC[A/G]AAGAAATTCTGTCTG	23077
rs561088932	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77204175	TAATATCCAGAATCT[A/G]CAATGAACTCAAACC	23077
rs561091662	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77079429	ACAAGTTCAATACAT[G/T]TTCAAACTAGTGTCA	23077
rs561094632	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77312305	AGCAATAGAAACAAT[A/T]AATATATAGGAAAAC	23077
rs561102333	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77174207	CTAAGAAGATACACT[A/G]TACAATTTAATTATA	23077
rs561108690	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77320314	CTGAAAGCCTAACCA[C/G]AGCACCTGCCACACC	23077
rs561119022	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77064910	CGTGATCCTATGGAA[A/G]ATTCAACTTCTAATC	23077
rs561134552	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77189174	TTTTGCCAGGTAATG[C/T]CAATACAGGGCTTTT	23077
rs561140092	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77053892	GTAAGTGCAAAGTAC[G/T]AGAGATAGAAAAATG	23077
rs561141028	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77173533	GGAAGCAGAAAATCT[A/G]TATCTAGGGAAATTA	23077
rs561156689	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77253995	AAATAAGCCCATCCA[C/T]CAACAGGAGAATGGA	23077
rs561158372	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77212876	AAAGAATGCTGACAT[A/T]GACTCAATAGATATT	23077
rs561171790	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77109961	CTGTTATCTTTGTAA[C/G]CTGAGAATGTACGTC	23077
rs561188631	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77305392	TCATGCTACAACATG[A/G]ATGAACCTTGAAAAC	23077
rs561188910	in-del	-/AAA			intron-variant	MYCBP2	GRCh38.p7	13:77106536	TGAGATAATACAGAT[-/AAA]AAAAATTTTTTTCAA	23077
rs561194573	snp	G/T	0.00835141	0.0640778	intron-variant	MYCBP2	GRCh38.p7	13:77102171	TTATCAGGATCATAC[G/T]ATATCATAATACTAT	23077
rs561201811	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77205656	ATGTCCTATGGTATT[A/G]ATGACATTAAATGCT	23077
rs561206228	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77328347	TTTTAAAGATAATTA[A/G]CAGTGGGATAAACAT	23077
rs561228449	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77071907	AATGAAACTGAACCA[A/G]AAATTAATAATATAA	23077
rs561233921	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77313970	TCTACTACACACCTA[C/T]CAGAATGGCCAAAAT	23077
rs561257050	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77237380	ATGATTATATTTTAA[C/T]AGAGTAAGATATTAG	23077
rs561261529	snp	A/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77129089	GCAAAGGTTTTAAAG[A/T]CACAAAATTTGTTAT	23077
rs561272831	in-del	-/GTG	0.00359065	0.0422189	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228695	AGATGAATATGTTGT[-/GTG]TGTGTGTGTGTGTGT	23077
rs561290012	snp	A/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77268437	GAGATATTTTAAACT[A/T]AGTTCAATTTTTAAG	23077
rs561291845	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77268354	TTGAACACACTGCTA[C/T]AATAATATACTTTCC	23077
rs561295431	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77088120	TTCACTGAAAGCACA[C/T]GGAACTTGAAACAGT	23077
rs561298218	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77288682	TAACTCTTAGAGTTC[A/T]GTATCAAAGGAAATT	23077
rs561306325	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77189709	ATATGCCTTTATACA[C/T]GCTTAAATTATTGTA	23077
rs561306793	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77278939	AAAAAATATATATAC[G/T]TTATGACATGTAAGC	23077
rs561313207	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77184708	ACAAAGGTTGTGGCT[C/T]CCTCATGAATGAATG	23077
rs561325724	snp	A/C	0.00438332	0.0466095	intron-variant	MYCBP2	GRCh38.p7	13:77275649	GCAATATAGTAAGAT[A/C]CTGTCCCTAAAGATA	23077
rs561333872	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77318481	AAATACTGGGCCAGG[C/T]GCAGTGGCTCACGCC	23077
rs561345275	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77148314	TTCACCTAGAACTCT[A/T]GTTTCTCATTCCCTG	23077
rs561403967	snp	A/C/G	0.00159649	0.0282165	intron-variant	MYCBP2	GRCh38.p7	13:77129751	AAAATAAAAAGTCTG[A/C/G]GTCATTTTTTTCAAT	23077
rs561414153	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77182155	AAGAAAAATCAGGCT[C/T]CTGTCCTCTAGTAAA	23077
rs561434063	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77065764	AGATTTTAAAGTCAC[A/G]TAACAATTCCCACAC	23077
rs561451590	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77230613	ATTACTCACATAGCC[A/G]AAAGATAATTTTATG	23077
rs561456218	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77126649	CAGTACTGTCAATAT[-/A]AAAAAAACACATAAC	23077
rs561469737	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77293136	AGCCTGAAGACAGAC[A/G]CATTTGGGATTAGGA	23077
rs561475462	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77120800	GCTGTATATATATTA[C/T]ATTCATATGACTTAG	23077
rs561495250	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77194556	AAAGGTGAGAGAACT[C/T]CAACAAAAAATTTTA	23077
rs561497109	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77276100	ATAATAACAGCAATA[A/G]TATCGCACATTCTTA	23077
rs561514574	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77245585	CACAGGAAAGGGAAC[A/T]TCACATACTGGGGCC	23077
rs561520438	snp	C/T	1.66593e-05	0.00288607	intron-variant	MYCBP2	GRCh38.p7	13:77068552	ATGGAAAGGCTGTAG[C/T]GTGATCAGTCACCTG	23077
rs561533124	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77200557	CGCCACAAAGATACT[C/T]CTTGAGAAGAGCAAC	23077
rs561548331	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77113246	ACCTGCCTCTTTTTT[G/T]AATGTTTCTCTAACC	23077
rs561548475	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77286569	CCATCCCGGCTAACA[A/C]GGTGAAACCCCGTCT	23077
rs561564051	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77072383	AATAAAAACAGAATA[C/T]CCCAAATTTGTGAAA	23077
rs561574670	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77124196	CCAGCTGTACAACCA[C/T]AGACACGTTAGTTTA	23077
rs561594086	snp	C/G	0.00557542	0.0525036	intron-variant	MYCBP2	GRCh38.p7	13:77157566	GCCTGGGCAACATGG[C/G]GAAACTCTGTTTCTA	23077
rs561602019	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77095837	AAAAATTTAACACCT[A/C]ACTAGTTAAATCTAA	23077
rs561615447	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77155263	ATGAAAGAATGCATG[A/C]AGTAGTTGAAATAGT	23077
rs561622841	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77084309	TCCATCTTGCTACCA[A/G]TGTAAGCCCATCAAA	23077
rs561638181	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77316895	GGAACACAGCCCTAC[C/T]TCCTCCACATGAACA	23077
rs561665416	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77141323	ACAATGTAGCATGGT[C/T]GTGAGAAGCTGAGGT	23077
rs561686893	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77101515	CAAATACCAGGAACA[C/T]CACTTGTCATATGTG	23077
rs561688917	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77092032	TCAAAGAAATTCTGA[C/T]GAGTAATCCACACAG	23077
rs561696793	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77279409	ATCAGGTGCAAGAAA[A/T]ATCAGACTCTATATC	23077
rs561739267	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77093024	CCTTAGTCATACATG[C/T]ATGCTTTTTCTTACT	23077
rs561741582	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77234060	CTCTTTCCACTTATA[C/T]GGTATTTAAGGAAAA	23077
rs561751164	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77247818	TTCAATAGAGAAAGG[A/G]TAATCATTTCAATAA	23077
rs561768228	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77240661	AAGCAGGCATCACTT[C/T]GCATAGTGCTGTGTT	23077
rs561769236	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77194446	GTTTTATGGTCTACA[A/T]TAATCTCTGTTTTCC	23077
rs561794458	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77060647	TAGGTTACCTTTTGT[C/T]TTATGTCTATTCATT	23077
rs561810405	snp	A/G	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77285921	AAGCAAAGGAAGGAA[A/G]GAAGGAGCTATTAGA	23077
rs561832560	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77093474	TCGTAGATGTAGGTA[C/G]GTGAAAATAAAAGTC	23077
rs561838491	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77183258	ACTCATAAAATTAGT[C/T]GGGAAGTGTTGCCTC	23077
rs561844440	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77170633	CCAGGCTGGAGTGCA[A/G]TGGTGCGATCTCGGC	23077
rs561846155	in-del	-/TTAT	0.00284299	0.0375954	intron-variant	MYCBP2	GRCh38.p7	13:77150984	AACCAAATACCATTA[-/TTAT]TTAATTGTCACTGAC	23077
rs561855627	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77132110	TACGAAACTTTAACA[C/T]TAAGCTAAAGAATGA	23077
rs561875042	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77201860	CGAGAACAAAGACGC[A/C]ACATACCAGAATCTC	23077
rs561888637	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77101243	ATCTGTAAACTGAAA[A/G]AGGTTTTCTCTCTAA	23077
rs561894826	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77300111	AAATAAAGAGATGAA[A/G]GAGACTGAGGTTCCT	23077
rs561905732	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77086377	GGCTGCTTAAAAGAT[C/T]TCTTTCTTTGTTTTT	23077
rs561907395	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77310769	ACACAGAGACACAGA[C/T]GTGTGTGCGTGCGCA	23077
rs561922988	snp	A/G	3.33311e-05	0.00408221	synonymous-codon, utr-variant-5-prime	MYCBP2	GRCh38.p7	13:77278813	CTGGCCCTGCAGCAC[A/G]TTGAGCAGGGCTTGG	23077
rs561926443	in-del	-/TTTAC			intron-variant	MYCBP2	GRCh38.p7	13:77299885	ATTTATCTTAAAATA[-/TTTAC]TTTAAAAATTCCAAA	23077
rs561935719	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77242736	ACAAGTTGTGAGAAT[A/G]TCTATTTTTAAAAAG	23077
rs561940318	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77272138	GCCAGCTCTGTATGC[C/T]GTGGCTACGCTATTT	23077
rs561944299	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77116583	TTGCGAATAAGAAGT[A/T]TAAAACAAGACCTAA	23077
rs561963556	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77135082	TTGGGATCCAAATAA[C/T]GTGCACACATTGATG	23077
rs561965618	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77094366	CAGAATACTAACAGG[G/T]TTCTATCTCCAGTAA	23077
rs561965790	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77085908	GTAGTTATGCAGGAA[C/T]AGATAGCTGTTACAG	23077
rs562008697	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77236377	AGAAAAAGCATGGAA[A/T]AAGTGGCAGTGTTAA	23077
rs562019051	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77265707	AGCTATTCCTACCCA[C/T]GAAAAACAAAAAGTG	23077
rs562047105	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77235848	TAAAAGAAACCACCA[C/T]ATAAGATGAGGTCAA	23077
rs562062668	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77216878	TATGTAGGAGGTAAC[A/G]GGCCATAATGTACAC	23077
rs562086837	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77309895	GAGGCGGGCAAATCA[C/T]GAGGTCAAGAGATGA	23077
rs562091393	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77133761	TAACTCTGAACATTT[A/G]ATTCTCTGTCTAGAA	23077
rs562118611	snp	C/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77286720	GAGATGGCACCACTG[C/T]ACTCCAGCCTGGGCA	23077
rs562126153	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77150595	GATAACATCATCTTA[A/G]TAAGTGTTGCTGCAA	23077
rs562128181	in-del	-/C	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77131037	AATTGCCAATAAAAT[-/C]AATTCTGTATATGCT	23077
rs562130333	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77163735	CATTCTCCCTCTCTA[C/T]TCTGAAAGTACTTAC	23077
rs562146814	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77196572	TTTGAAAGTGGAAAC[A/G]ATAATATTTGCTCCC	23077
rs562153676	snp	A/C	0.0193772	0.0965046	intron-variant	MYCBP2	GRCh38.p7	13:77046904	ATTGGTGCCCACCCC[A/C]CCAGTGGGTGGGGGA	23077
rs562154194	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77286063	AAGTTCACAAAACTT[C/G]TATTACTCTATGAAA	23077
rs562159761	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77052274	CGCAATCATGGCTCC[C/T]GACAGCCTCAACCTC	23077
rs562168911	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77160905	TGATAAAAAGTAGTA[C/T]ATTTTTAAAGAGTGT	23077
rs562169633	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77250325	ACTTAGAAATAAACT[A/C]CTATTAGATCCAGAC	23077
rs562187417	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77157178	CCGCCTCTAGGGTTT[A/G]AGCAATCCTCCCACC	23077
rs562187518	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77149816	TCTACTGATTCTATT[A/G]AATCTATCCTCATTG	23077
rs562187843	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77190805	GTGATTTTTCTACAG[C/T]AGTCTCCTTGAATAT	23077
rs562202890	snp	G/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77195460	AAATTAGCTGGGCGT[G/T]GTGGCACATGCCTGT	23077
rs562215093	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77193867	CAAACTAGGTATTCC[A/G]TAAGAGATGCATGAA	23077
rs562222799	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77220526	CTTCATTATCATGCA[C/T]ACCACAATATTGATC	23077
rs562223059	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77302065	GAGACATGTGGGACA[A/G]AGTCAGATGGTCTCA	23077
rs562225207	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77249684	ACAGACATGGGCCAC[C/T]ACACCCAGCTAACAC	23077
rs562242065	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77077442	GATCACTTTTATCAC[C/T]GTGCTGGACTTAGCA	23077
rs562251805	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77230113	CTCTGCTTTGCCTTT[A/C]GTCAATATCTGCCTG	23077
rs562276194	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77135173	GCAACTTTTCAGTAC[C/T]TTCACTTCTTTTTAA	23077
rs562309948	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77171060	AAAGAGAGGAGAATA[C/T]AAACTAGAGAGATTC	23077
rs562349937	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77179717	GTATTTCTCTAGGGT[C/T]GGTTGAGTGGGCAGA	23077
rs562372306	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77170662	GCTCACTGCAGCCTC[C/T]GCCTCCTGGGTTCAA	23077
rs562373245	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77249644	AAGTGATCCTCTGGC[C/T]TCAGCCTCCCAAAGT	23077
rs562376719	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77135980	AGCTGGGACTATAGG[C/T]GTCCACCACCACGCC	23077
rs562379213	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77226354	GCATCAAAAACCACA[G/T]TCCAGAATATAAAAA	23077
rs562390951	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77046118	CTTTGGGGAAGATAT[G/T]AATTTGTTGATAATA	23077
rs562391651	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77295666	AGCTATTCAGGAATC[A/G]TAGTTACGACTCCTC	23077
rs562407682	snp	C/T	3.29587e-05	0.00405934	splice-acceptor-variant	MYCBP2	GRCh38.p7	13:77243162	GGGCACTGGGACAGC[C/T]AGATGATTGGCCAAA	23077
rs562426525	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77178463	TGAAGAAAATGGTCT[A/C]TACCCTAAGATTGAA	23077
rs562435841	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77310574	ATATGTCATATATAT[G/T]ATTATAGACACATAT	23077
rs562450389	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77180784	AGTTAGCTGGGTGTG[A/G]TGGTATGTGCCTACA	23077
rs562456299	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77053087	AGGCTGCAGTAAGCT[G/T]AGATCATGCCACTGC	23077
rs562461888	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77234191	AATTTTAGGTTTTTT[C/T]CTTATACAGCAGAAC	23077
rs562463207	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77205938	AGGAAGACACATTAG[C/T]GTCACACAAACTTAA	23077
rs562476828	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77177629	GGCCAGTCTTTTTCA[A/T]TTTCTTTAGTGTCAT	23077
rs562498158	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77084548	GACTTTGTTAGACTG[A/G]GGTTATTTCAGTTTT	23077
rs562501791	snp	A/C	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77133436	AAAACCTACTATGAG[A/C]AAAGTGTAATTTTTA	23077
rs562513180	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77185742	TCATAGCAAGCTGAC[C/T]TTCTCCCCTCATTTT	23077
rs562529920	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77134658	TGCCTCACAGAGGAT[C/G]TGAACCCTTCATCTA	23077
rs562535089	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77240774	TGGTTCCAATGTGCA[C/G]ACATTTCTGTTAATT	23077
rs562539091	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77225352	AACACACAGTTAACA[A/G]GCTATGTTCATCAAA	23077
rs562555000	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77146643	AGTCAAGACAATTCT[A/C]TGAAGAAGAAATCTG	23077
rs562562490	snp	A/G	0.0134861	0.0810011	intron-variant	MYCBP2	GRCh38.p7	13:77202422	TTACCAACCAAAAAG[A/G]GTCCAGGACCAGATG	23077
rs562571248	snp	A/G	2.2538e-05	0.00335686	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076712	CTGAAAAAAAGAATA[A/G]AAAAGGGAAATAAAT	23077
rs562572701	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77311074	TTTCCCAGTTTGGTT[A/G]TTTTTCTCCTTTCAC	23077
rs562575414	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77234697	AATGTAATAAAATTG[A/G]TATTTCAAATATGAA	23077
rs562580511	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77325192	CCATGATACCTAGTG[A/C]TAAGCTACAAATACC	23077
rs562604849	snp	A/G	0.000247119	0.011113	synonymous-codon	MYCBP2	GRCh38.p7	13:77068703	CAGCTCAAAGCAGTA[A/G]GCATCAGAGGAGGCA	23077
rs562619844	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77199317	TCACTCCCACCTGAA[C/T]ACTGCACTTTTCTGA	23077
rs562627004	in-del	-/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77213482	GCTCTGTCTCAAAAA[-/G]GAAAAAAAAAAGTAA	23077
rs562641829	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77197122	GATGAGAGCTGAGGC[C/T]TGACTATTGAATTTA	23077
rs562653824	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77046940	CGCAGGATGGGGACA[C/T]TCAATGGCAGATCTA	23077
rs562658435	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77231717	AACTGTTTCATGAAA[C/T]GTGAATATTTAACCT	23077
rs562663812	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77264729	CTCAATTGTAACAAG[C/G]GATACCAGTATTACA	23077
rs562683560	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77116877	TTGTTTTTGTAAAGA[C/T]TTGCAATGATTCTTT	23077
rs562684174	snp	A/C/G	9.896e-05	0.00703358	missense	MYCBP2	GRCh38.p7	13:77217944	GCAATGCTTGAACAA[A/C/G]AGTGGGACATCCCCT	23077
rs562687046	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77218613	GAGAATACTAACAAA[C/T]GGTGTCTACCCCCAC	23077
rs562691028	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77094426	TCCACATTCCACAGT[A/G]ATTTTTTAATTGCAA	23077
rs562719640	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77150643	TGCTCTTTGGACTTA[A/C]AATTTCATGTCTGCA	23077
rs562755650	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77102177	GGATCATACTATATC[A/G]TAATACTATATGCAT	23077
rs562771550	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77077612	GGTTAATACAGGTTA[A/C]GGGATTTTCAGTAAA	23077
rs562784058	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77157327	CCTCCAGGGTTTGAG[C/G]AATCCTTCCACCTCA	23077
rs562812182	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77243262	AAAGCTAGCAAAAAC[A/G]TTGTCTAAAACACAC	23077
rs562841657	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77079197	CTTTCAACAAATCTG[C/T]TTGTCACTTATGTCA	23077
rs562846653	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77210693	CTTTGGCATAATTTC[C/T]TCCTCATAGTTAATA	23077
rs562867804	snp	G/T	0.00079936	0.019976	intron-variant	MYCBP2	GRCh38.p7	13:77258877	TATTTTTTGCAGGTA[G/T]AAAAAAACAAAAAGA	23077
rs562893066	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77236101	AAGATAAGACTGGAG[A/G]TAAGGCCAGTTAAAA	23077
rs562921881	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77236475	TCTAGTAACTGCACC[C/G]TAGGAATCTATCCTA	23077
rs562922749	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77143720	CAATTTCATCATTGT[G/T]CAAACATCAGAGTGG	23077
rs562952214	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77188270	ACATTCTTCCTATGC[A/G]TTTTACTAATATGAA	23077
rs562976953	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77088036	TGATCCTCCCTCCTC[C/T]GCCTCCCAAAGTGCT	23077
rs562985801	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77143118	AAAGAAAAGATTAAT[C/G]CCTAAAACAAAAGAA	23077
rs562988154	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77241292	ACCTAGAGAAGAATA[C/G]CTTTTTTAGAGGGAA	23077
rs562999301	snp	C/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77187774	TGGGAAGGCCGGGTG[C/T]GGTGGCTCACACCTG	23077
rs563003408	in-del	-/A	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77133364	CAGAATGATCATATC[-/A]AATGCAAAGAACTAA	23077
rs563005652	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77242848	AATTAAAAGTATGTT[A/G]TTAGCACAATTATAA	23077
rs563014684	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77119158	ATTTGAATAGTATCT[-/A]AAAATATCGATTCTA	23077
rs563016951	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77151148	ATGAACCATGAACAC[A/G]GTGTAAAAACAAGGC	23077
rs563031868	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77203598	ACCAAGTCAATCCTA[A/C]GCCAAAAGAACAAAG	23077
rs563037257	snp	A/T	1.67211e-05	0.00289142	intron-variant	MYCBP2	GRCh38.p7	13:77090278	ACTGTACATGGAACA[A/T]TGCAACAGATACAAA	23077
rs563044890	snp	A/G	0.000584624	0.0170871	intron-variant	MYCBP2	GRCh38.p7	13:77070728	TTTACATAGAAAAAG[A/G]AAAAAAAAAAAAAGA	23077
rs563055009	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77266761	GAAAAAAAAAAAAAA[A/C]AAAAAAACCCTGTAG	23077
rs563070435	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77288705	AGGAAATTCATTTTA[C/T]GACTTCCTAAGAGAC	23077
rs563073078	snp	G/T			upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77328083	TCCTGACAAAATAAT[G/T]TATAAGTTCTGTCAT	23077
rs563075507	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77199035	ACTGTAGGGGGGGAG[A/G]AGGCAAGATGGCTGA	23077
rs563121020	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77060097	CTACCTCAGGAACTC[C/T]GCAATTTGAAAAGGA	23077
rs563138411	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77193405	GATCATCCTTGTTTC[C/T]GAAAATATACATTTT	23077
rs563160076	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77158600	AGGCGTATGCCACCA[A/T]GGCTGGCTAATTTTT	23077
rs563160686	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77172089	TGTTTTTAGTAGAGA[C/T]GGGGTTTCACCACGT	23077
rs563160837	snp	A/C	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77281648	AAATAATTACCTGAT[A/C]CAGCCAGTCTAATAT	23077
rs563164042	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77306631	GACCCTGCCTCATGC[A/G]TATTTGTACTCTTAA	23077
rs563169664	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77128673	GAACTGTGCCTATCA[C/T]GCTCAAGCAATAGTA	23077
rs563172334	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77091163	GGCTAACTGCCTAGG[C/T]GTTTTCTTTACTCAC	23077
rs563176923	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77164947	GTTGCACAAACTCCA[A/T]CCTCTTCATGTATTA	23077
rs563192898	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77238886	CTGTACTCCCAGCAC[C/T]TTGGGAGGCTGATCA	23077
rs563202278	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77237216	TAGGTAGTTACTGTA[C/T]AGAATGTGGTAGATC	23077
rs563206484	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77115941	AATATAAATTAAAAA[A/T]ATATATATATTAAAG	23077
rs563209192	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77294734	TGTATATTGACAATG[C/T]GCTCCACTTCCCTCC	23077
rs563227919	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77254203	TGTGTAAAACAGACA[A/T]CATTATGCAATATTA	23077
rs563228167	snp	A/G	0.000314026	0.0125266	synonymous-codon	MYCBP2	GRCh38.p7	13:77098391	TTCCTGTACCACATG[A/G]GGAGAGGGAGCTCTA	23077
rs563229755	snp	A/C	0.000198813	0.00996829	intron-variant	MYCBP2	GRCh38.p7	13:77262035	ATGCTCATTTTTAAT[A/C]CAAAGAGAATAATTT	23077
rs563232097	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77191444	AAACAATGTAATACC[C/T]AGAAATATATACAAA	23077
rs563234238	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77230023	TAATTCTGTTTCGAA[G/T]ATAGTTTATAGGCAC	23077
rs563243869	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77327050	TGCCGCCGCCACCAC[C/T]GCTACCACCGCCACC	23077
rs563252799	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77298787	CAAGATAGTATGCCA[C/T]AAAAGTAAAGAGAAA	23077
rs563254415	snp	A/G			intron-variant, utr-variant-5-prime	MYCBP2	GRCh38.p7	13:77227108	ATTTCTTGAGCCCTT[A/G]GTTTGAAAAGCTAGT	23077
rs563272030	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77252448	ATAACCAAATAAAAA[C/T]GTAAACTACAACTGG	23077
rs563279120	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77153112	ATTCACGCATTCATC[A/G]CGTTTCAAACCATTC	23077
rs563299214	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77259502	AGCAAGCAACAATTA[C/T]ATTGAATATTATTTT	23077
rs563314977	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77261514	TTTTTTACACTATTC[A/G]GCTTCTGGGAGTTGA	23077
rs563318457	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77064220	AGGGCTCTACATTAG[C/G]AACAACCAGGCATAG	23077
rs563331223	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77146592	CATATAGAGAATAAA[C/T]CCATACAAAAGAGAT	23077
rs563339367	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77160216	GGATTACAGGCATGC[A/G]CCACCACGCCCAGCT	23077
rs563357561	in-del	-/A	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77265465	TACAATCTGTAAGAT[-/A]AGCCGAGGTTTAAAG	23077
rs563388677	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77254833	TCAATTTTTTAGTTC[C/T]CATATATGAGTGATA	23077
rs563392320	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77255385	ATTAAAAAAATCTTT[G/T]AACAATTTTACTTTG	23077
rs563392937	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77146110	GGATGATTTTAGTTG[C/T]AAGCAGCTGACAACA	23077
rs563405807	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77100608	ATGGTGAAATAATAG[A/T]GTATGGCAAGTACTT	23077
rs563410999	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77131782	CAGAAAAGTTCTGTC[A/G]AGAAAATTAGAAAAT	23077
rs563417343	snp	G/T	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77184561	GATGTTTTTGGCCTA[G/T]TTCCTCTATTAATTA	23077
rs563419806	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77108166	ATCTGAATGTGGAAA[G/T]AAGATGGGACACATA	23077
rs563439907	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77239512	GACCCATAAATTCTG[A/C]TTCATTAGGCCCAGG	23077
rs563440334	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77283955	TAAAATCTGTAAAGT[G/T]TTAGAGGATGTAGAT	23077
rs563453486	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77212910	CCACCCCTGGCTCGG[C/G]ACCTCTCTCCCCTCA	23077
rs563466108	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77183894	CATGTTTTTTCTTTC[G/T]CTCTTCTCTCCCAGT	23077
rs563467678	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77249188	AGTTATGGAGATGCA[G/T]GGTGGTAATAGTTGC	23077
rs563473764	snp	A/C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77286612	CAAAAAAAAATTAGC[A/C/T]GGGCGCGGTGGCAGG	23077
rs563479578	in-del	-/CTGT			intron-variant	MYCBP2	GRCh38.p7	13:77310398	GCCAAAAACAGCTTC[-/CTGT]CTATCTTTGTAAATA	23077
rs563490310	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77239060	GAGAGGCGGAGGTTG[C/T]AGTGAGCCGAGATCG	23077
rs563506411	snp	A/C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77192404	GTCACATAATATCTA[A/C/T]ACAAACATTATTAAT	23077
rs563519821	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77147572	TTCCTTCTCTCTACC[C/T]TTTTTGTTTTCATAA	23077
rs563526692	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77246718	CTTATGAATAATGAT[A/G]TGAAAATCCTCAACA	23077
rs563556814	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77175445	TTAAAATGTGAGCTA[C/T]AGAAACTAATGCTTT	23077
rs563560794	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77284878	GACAAAACTGAGGCA[C/T]GGATGTGTCAAATAA	23077
rs563571596	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77123066	TCAAAGACCAATAGA[G/T]AATTTTTACAAAGAG	23077
rs563580213	snp	A/C	0.00557542	0.0525036	intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77325437	AACCTTCAGGGTATG[A/C]GGCATGTAAGGGCAT	23077
rs563599213	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77141496	GTACAAGGGGCCAGG[C/T]GCAGTGGTTCACAAT	23077
rs563637101	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77131167	AATGTCCTAATAAAA[C/T]TGCATTTATCAAGAA	23077
rs563637907	snp	A/C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77304165	CCGTATGTTGAAAAG[A/C/G]TTCAGAACTCCCATG	23077
rs563641678	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77169138	AACAGGCCGGGCGCG[A/G]TGGCTCACGCCTGTA	23077
rs563649620	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77058135	ATGAGCCACTGCGCC[C/T]GGCCTCAATCAATGT	23077
rs563654721	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77271232	TAATTCTCAATAATG[A/G]TGCCTTTTTCCATGT	23077
rs563658464	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77196547	AGAAGTGGTTAGATA[C/T]GGGATTTATTTTGAA	23077
rs563660531	snp	C/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77148530	GAAATTTCTTCCCTT[C/G]CAAACTAAATTAGGT	23077
rs563668348	snp	C/T			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77079198	TTTCAACAAATCTGC[C/T]TGTCACTTATGTCAG	23077
rs563703463	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77192672	ACAGCTGTAGAAGAG[C/T]AGTGGTAGAAAGTCA	23077
rs563705442	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77273035	GAAGTAACTCAGAAA[C/T]GAATCAATTCATAAA	23077
rs563706565	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	MYCBP2	GRCh38.p7	13:77045220	TCATAGCAAGAATTA[C/T]GTACATGGTATTTGG	23077
rs563714538	snp	G/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77155357	AATCAGCTCTAAGCT[G/T]CAAACAACCAATCAC	23077
rs563717157	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77176216	TAATGATCTGCCAGT[A/G]TCTTAAAGTCAGCAT	23077
rs563720744	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77101079	GTGATGTTTGGAATA[C/G]TTGTTTTTTGTTATT	23077
rs563723435	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77051583	AAGAAAATTTATTAC[A/G]TTGTTTAACTATGGT	23077
rs563742466	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77299740	CTAAATCAATCGAAG[C/G]TTAATGAAGAATGTC	23077
rs563742661	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77066644	TTAGAAGTAGAATTG[C/G]TAGGTCAAAAGATAT	23077
rs563749189	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77277999	CATGTTGAGTCTGGG[C/T]CACTGATATGAAAGG	23077
rs563764442	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77308264	TACTCCCTTTGCTTT[C/T]CTTCCACCCACCTTG	23077
rs563770753	snp	G/T	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77258825	CTACCTCCTATAATC[G/T]TCATAACAACTATAT	23077
rs563770918	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77299444	TTTACTGTGTTTTTT[G/T]TTGTTGTTGTTGATT	23077
rs563777451	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77109751	GGGACTGGCTGGAAC[C/T]GTGGCAGAGGAACAT	23077
rs563782282	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77301811	TGCAGAGATTAACAA[C/T]ATGTGTAAAATAATG	23077
rs563787069	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77058853	AACCAGGCATGGTGG[C/T]GCGCGCCTGTAATCC	23077
rs563805065	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77235209	ACAGAAATAAAAACA[C/T]AAACTATGAAATATT	23077
rs563805808	in-del	-/A	0.00239425	0.0345166	intron-variant	MYCBP2	GRCh38.p7	13:77258877	ATTTTTTGCAGGTAG[-/A]AAAAAAACAAAAAGA	23077
rs563808862	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77161838	GTCAAGACAAATAGG[C/T]TGATCTGAGTGACAA	23077
rs563815273	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77183935	AGGAGTTTACCAACT[A/T]TTTTTCTTCAAAAAA	23077
rs563816782	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77142974	CCCAAACCAGGTTTT[C/T]GAAATTTATCTGATC	23077
rs563859784	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77052201	TCTCCTCTTCCACCT[C/T]TCTCTCTGTTTCTTT	23077
rs563896633	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77200031	CCAGCAACGGAACAA[A/G]GCTGGATGGAGAATG	23077
rs563898258	in-del	-/A	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77101938	CTTCAGACTATACGT[-/A]AATACTTTCACATTC	23077
rs563905605	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075202	GACAGAGAGAGACCC[A/G]GTCTCAAGCAAAACA	23077
rs563922466	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77099369	TCTTTTGGGGAATAA[G/T]AAATTATTTAATGTG	23077
rs563947989	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77209335	TGTTATTGCTAACTT[A/G]GTGAATGCATCCAGA	23077
rs563950864	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77184588	ATTACTGAAAGAGGA[G/T]TGTTAAAGTCCCCAG	23077
rs563956663	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77263125	AATACTCTGTGGTTA[C/T]CTGTATTTCTCTATC	23077
rs563960788	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77293308	CCAGAAAAAATAATA[A/G]GATAGTCTGGCTATG	23077
rs563966224	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77194645	GCTTCATCACTTACT[A/C]ACTGAGATCCTGGGA	23077
rs563992388	snp	C/T	1.65228e-05	0.00287422	synonymous-codon	MYCBP2	GRCh38.p7	13:77224480	TCCATGTCCTAGCTG[C/T]CCATGCTGCCCATAA	23077
rs563994415	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77215846	CTGGCCTGCCAAAGT[G/T]CTGGGATTATAGGTA	23077
rs564015734	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77091909	GTCAGACTAGCCTCA[A/G]AACAGTTTCTAACTC	23077
rs564023130	snp	A/T	1.8783e-05	0.0030645	intron-variant	MYCBP2	GRCh38.p7	13:77099068	TATAACTTACTGATA[A/T]TTTAGCCACTAAACA	23077
rs564024291	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77301222	GAGTTCGAGACCAGC[G/T]TGGCCAACATGGTGA	23077
rs564026877	snp	C/T	9.89919e-05	0.00703464	missense	MYCBP2	GRCh38.p7	13:77180308	GTCATCCCTGAGATA[C/T]TCTCTTCACTCTGCG	23077
rs564030106	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77208532	CTACAGAATTCCACA[A/G]TTTTAATAATGAAGC	23077
rs564036271	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77239158	AGTTCTGATCATCTA[C/T]GAAAAACTTAGTTCA	23077
rs564043340	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77067502	ACCTAACAAGGTAAA[A/T]TCTGAAATTATGTCT	23077
rs564044345	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77147339	TGTTTCTTAATAAAA[A/T]AATAACAAAATGACC	23077
rs564048037	in-del	-/T			intron-variant	MYCBP2	GRCh38.p7	13:77054603	GAGATTGGTAAAGTC[-/T]TTTTTTTTTTTTTTT	23077
rs564060746	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77199936	ATAAAACCACAAAGA[C/T]GGGGAAAAAACAGAG	23077
rs564061800	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77210279	CTCACTGCAAATTCC[A/G]CCTCCCAGGTTCACG	23077
rs564069575	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77091250	ACTGATTGGCAGTAA[A/G]TGTCCCTGGGTGTTA	23077
rs564096141	snp	A/C	0.00874735	0.0655527	intron-variant	MYCBP2	GRCh38.p7	13:77285862	GAGAAAGGAAGGGAA[A/C]GGAAAGGAAAGGAAA	23077
rs564110079	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77240541	TGAACCTGGGAGGGA[C/G]AGGTTGCAGTGGGCC	23077
rs564111878	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77199583	TAGGCTCCACCTCTG[C/G]GGGCAGGGCACAGAC	23077
rs564121272	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77140257	GCAGGTTTGAAAGTA[C/T]CGTAATTCTTAATAA	23077
rs564180481	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77068471	GAAATAAAAATCTAT[A/C]CTTAGGGTCCTTAGA	23077
rs564188258	snp	A/C	0.00478085	0.0486577	intron-variant	MYCBP2	GRCh38.p7	13:77139729	AGTTAAAGCAGTAAG[A/C]AACACATTTCAAAAC	23077
rs564205314	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77082356	TGCCATACTAATTCA[C/T]CAGGGTATAGTTTAT	23077
rs564215585	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77120843	TTTACAACTTTCTGG[A/T]TTTATTATAGATATT	23077
rs564225965	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77109136	TTCTTATGTGGCAGG[C/T]AGAGGACGGTTTCCT	23077
rs564265534	snp	A/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77233946	GGCACCTAACCCAAA[A/T]AACATTTTGGAAACA	23077
rs564273597	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77323011	CTCTTCAAGTCCCCA[C/G]ACCCCTCATTCTCAG	23077
rs564281398	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77176440	GGAATACTCTTCACT[A/G]TTTTAACTACATAAT	23077
rs564285455	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77233060	ATAGAAGCAAAGTAG[A/G]AGAATCAGGTTTGTG	23077
rs564289110	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77108788	AGCTCACTGCAAGCT[C/T]TGCCTCCCAGGTTTA	23077
rs564313949	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77285081	TCTGTTAATTATGCT[A/G]CAAAAGGTTATCTTA	23077
rs564324887	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77115898	CAATCTGAACAAAGC[C/T]AATACTCTAGATGCC	23077
rs564340086	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77249673	GTGCTGGGATTACAG[A/G]CATGGGCCACTACAC	23077
rs564349450	snp	A/G	0.000108491	0.00736436	intron-variant	MYCBP2	GRCh38.p7	13:77169566	AAGTCTTTTTTTAAA[A/G]AAGATATTTAAAAAA	23077
rs564354928	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77153020	CAGTGAGCTGAAATC[A/G]TGCCACTGTACTCCA	23077
rs564364655	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77101092	TACTTGTTTTTTGTT[A/G]TTAATCTGACAGCTG	23077
rs564391882	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77323668	GCAGAGACTTTGTCT[A/G]TCTTGCTCACCGCTA	23077
rs564394506	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77134362	TGGTAAAACCCTGCC[C/T]GTCTCTACTAAAAAT	23077
rs564397096	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77133036	AAGTATTTATCTTTC[C/T]GTAGTTTGGCAGTTC	23077
rs564426678	in-del	-/TATAA	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77217730	TGCATATGTAACAAT[-/TATAA]TATAATTGTTATATT	23077
rs564436765	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77162569	GCTCCCTTAAAACTA[C/T]CCAGTGTCAACAGCC	23077
rs564443352	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77264533	TCACAGCATTTTTAG[C/T]ATTTAGTGTGCTCTA	23077
rs564449939	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77241730	CTTATCAGATGCTAT[A/G]AAGAACACTCTTCAT	23077
rs564451899	snp	A/C	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77250073	CTAAAAATACAAAAA[A/C]TTAGCCGGGCGTAGT	23077
rs564462965	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77264070	ATGAATTTACTCCTC[A/T]GTTGAAGTCAAAATG	23077
rs564468370	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77275770	GGGCAAATCACCTGA[A/G]GTCAGGAGTTTGAGA	23077
rs564482004	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77216326	TGCCTACTGGAGTTG[-/A]AAAAAAATCACCATT	23077
rs564482349	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77093489	GGTGAAAATAAAAGT[C/G]TGATAATTTTATTCA	23077
rs564484118	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77141817	AAATTTAGATATATA[C/T]TAAATGCACAATAAA	23077
rs564525831	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77201643	ACCACATACTTGGAA[A/G]TAAAGCTCTCCTCAG	23077
rs564557930	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77190061	TTTAAAGTTAAGCCT[A/G]TATGGAAAATGTTTA	23077
rs564558428	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77052893	CAGCACTTTGGGAGG[G/T]TGAGGCAGACAGATT	23077
rs564560990	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77257342	AACAGGGTGGCTACA[A/G]TTGGCGATAATTTTT	23077
rs564578258	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77309191	CTCACTTTCCCACTT[C/T]TCCCTGCCTCCTGAA	23077
rs564621275	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77246873	AAGAAAAGAAACACA[C/T]GATCATCTCAATTGA	23077
rs564623252	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77085796	ACTATGTAACCAAAA[C/T]AGGAAAGAGTCATTC	23077
rs564624776	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77112139	CTCCATGGTAACTCC[A/G]AGCTGATAAGTGCTT	23077
rs564634061	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77210325	AGCCTCCCGAGTAGC[A/T]GGGATTACAGGTGCC	23077
rs564644006	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77142279	CTCATTAAAGTGTTA[A/C]CACTTGACAGGAATT	23077
rs564701363	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77301843	AATTGGCAATTTTCA[A/G]CATAATTTATAAAAA	23077
rs564707605	snp	C/T	0.000399281	0.0141238	synonymous-codon	MYCBP2	GRCh38.p7	13:77156184	CTGAGGATCCGCATA[C/T]GAATCTGGCTGAAGC	23077
rs564719264	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77144392	GAAGATAAAAATAAT[C/T]TTGACTCTAGTTATT	23077
rs564731688	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77253049	TTATAAAGAAAAAGG[C/T]TGAAAATTTTGACAT	23077
rs564773724	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77234875	TCTGATTTCTATGGT[A/C]TGCCTACAATATTGT	23077
rs564778983	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77045917	TTTCTATAAGTAAAA[A/G]CATTTAAGTTTAAAG	23077
rs564780511	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77055974	TGGGGCAAATGGGAC[A/G]CAGAGCATGAAAATT	23077
rs564797939	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77213484	CTCTGTCTCAAAAAG[-/A]AAAAAAAAAGTAAAT	23077
rs564806745	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77245780	ACACACACACACACA[C/T]ACAAAGGAAATAAAA	23077
rs564819377	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77193054	GAATCGCTTAAATCC[A/G]GGAGGCAGAGGTTGC	23077
rs564820747	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77294576	TTCCTGGATATCATA[C/T]GCCACCACTTCAGGA	23077
rs564834710	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77244399	AAGCTTGCCAGCTTC[A/C]TGTAATATGTCTCCT	23077
rs564840903	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77165627	TTGTTACTTTTTTTC[A/C]TAATCAAACTCCCCT	23077
rs564843741	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77245138	GTGGAGAAATAGGAA[C/T]GCTTTTACACTGTTG	23077
rs564848035	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77259685	ATTTCCCCAGCATGG[A/G]ACAATTACATATATT	23077
rs564869439	snp	C/G			intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77074665	CCATATAATGGAACA[C/G]TTCTCAGCAACCAAA	23077
rs564875854	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77212962	CCTGGAGCACTGCGA[A/G]CACTCTGGTCACGTT	23077
rs564901744	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77164993	ACCACTGCACATAAA[A/C]TACAAAAATTTAGAA	23077
rs564906935	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77283625	TTATGCACCAGGCAC[A/G]GTGACTCCTGCCTGT	23077
rs564907566	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77119558	GAAAAAAAAACTTAC[A/G]AAAAACAGCTCTTCG	23077
rs564921476	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77048708	AAATGGAGCAAATAT[A/G]TGTGAAAATGCCCAG	23077
rs564926456	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77138666	GAGGTACAATGAATT[C/T]TCTCAAAGACTAGGA	23077
rs564941565	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77172546	AGGGAGACTAGTTTA[G/T]AGGCTTATTACAGTT	23077
rs564944502	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77282867	CTTTTTCAGTCGTTA[C/T]AGCCAATTTATTACT	23077
rs564953369	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77213489	TCTCAAAAAGAAAAA[A/C]AAAAGTAAATAGTGA	23077
rs564963545	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77313092	AATAACAATAATATA[C/T]TAATATGTAAGAAAA	23077
rs564964808	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77124158	ATGAAGATTCTGGCT[A/G]AAGTCTTACATCTGC	23077
rs564976097	snp	A/C	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77312361	GTTCTATAAAGTACA[A/C]ATGACTGTCGACAAC	23077
rs564994424	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77199210	GAGCTGAAGCAGGGC[A/G]AGGCATTGCCTCACT	23077
rs565001960	snp	C/T			missense	MYCBP2	GRCh38.p7	13:77097570	TTCTCACACTCTTTC[C/T]TTTTAAGAACTGCAC	23077
rs565004836	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77237970	AGCAACATGCCGGAC[A/G]CGGTGGCTCACGCCT	23077
rs565020268	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77276288	TCAAGATGTTCCACA[A/G]TAAGAGTTATATAAA	23077
rs565035110	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77230793	AGGGCTGAGAGGATT[A/G]CTTTCACTTTAGGAC	23077
rs565042274	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77096851	ACATTTGAGGTATAA[C/T]ATGTAGACAAAGAAA	23077
rs565067109	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77130316	AAACTTTTCTCATTA[A/T]CTCATTTTAGATAAT	23077
rs565090165	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77071208	GTGCACGCTGTTCTT[C/T]TAAGTGCCACATATG	23077
rs565097709	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77197781	CATACATTACAGAGA[A/G]GTGAAGGGAAGGAAA	23077
rs565101291	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77168206	TAGGAAGATTTAAGA[A/G]CAACTCTCATAAACC	23077
rs565107554	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77305594	ACAAAAATGTTTAGT[C/T]GTATGACTTTGTGAA	23077
rs565110103	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77206504	ATTGTTTTCTGTGGA[A/G]TTAGCCTCTTAGAGG	23077
rs565123008	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77129895	AAATGTAATCAATTT[C/T]ATCAAAAGACAGGCC	23077
rs565130578	snp	C/T			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075913	ACAAAAACAGGACAA[C/T]GATTAGATACTACTG	23077
rs565143098	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77323633	TCTATTTCTCCCATT[A/G]GAGTGGATTTTCCAA	23077
rs565161315	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77089767	GTGGAGAGATAACTG[A/T]GAATGTGTACGTCAT	23077
rs565163027	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77167466	AGTTTCTTCAACAAA[C/T]AGAACTCAAGGGAAC	23077
rs565163690	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77224720	TATTTTTGTAGGTCA[C/T]ATAAATGTATAATTT	23077
rs565169624	snp	G/T			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77080160	GGTCTGAGGAGGAAA[G/T]AGCTCATATTATATT	23077
rs565175346	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228051	CAGAATTAAAATATA[C/T]ATTTTATATATATAT	23077
rs565175385	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77189897	ATCTATAGTCCTCCC[A/C]ATCTTCCCTGCAATC	23077
rs565177267	snp	C/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77198894	ATTGCTAGGCCACCA[C/G]AAGTTCCACAGAAAG	23077
rs565181190	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77302731	TGTATCTCAAGCACA[A/C]TCTCCAGTGTCCCAA	23077
rs565183908	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77259052	TTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC	23077
rs565190424	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77231716	AAACTGTTTCATGAA[A/G]TGTGAATATTTAACC	23077
rs565202408	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77144987	GTTCTCTCTCATGCA[G/T]CATCAATTACTCTCA	23077
rs565209260	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77112714	CAAATGCTGGGAATA[C/T]AGGTGTGAGCCACTA	23077
rs565218863	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77320973	GTAACCAGGGGTAGG[A/C]GGGCCTGACAGAACT	23077
rs565233718	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77307184	CTCCTTCCCCCATCC[A/C]AAAAGAGACAGCTCT	23077
rs565239628	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77161054	CACCATTGCTAGATG[A/C]AAAATTTTCCCCATC	23077
rs565244008	snp	A/T	0.00119737	0.0244387	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081045	AGAGTAATTTTTTAG[A/T]GGAGTTACTTAGAAT	23077
rs565255088	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77182828	GAGTGTAGATACCAC[A/G]TGTCTTGTTTCCAAA	23077
rs565289271	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77290938	ATCAAAAATATATAA[G/T]AATTGTAAATAAAAG	23077
rs565291810	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77191068	TACAGGTCTGACCTT[G/T]GTTTTAACCACATGA	23077
rs565302446	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77262778	GCTTTACATATGGTA[A/C]ATTTTATGACTTTGT	23077
rs565308462	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77314014	AACATCAAATGTTGG[A/C]GAGGCTTTAATGCAA	23077
rs565331190	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	MYCBP2	GRCh38.p7	13:77044789	CTCAAACTTAACCTA[A/G]AAGTTTAAATGAAAT	23077
rs565334676	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77221984	AAACACCATGTTAAT[A/C]GTTGTTATACTCTGT	23077
rs565336023	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77048662	TCCATTTGATAACAT[A/C]GGGATAATACCATCT	23077
rs565367628	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77115325	ACTAAAATTTTTTTG[C/T]CAAATTGCTTACCAA	23077
rs565383665	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77073232	GCATAGCAATATATG[C/G]ATTATCTTACGGAAT	23077
rs565384143	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77269256	AACACTGTTTCCTAG[A/C]AAGTACTGAATCTAG	23077
rs565406901	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77266064	GAATAAAGACATTAA[C/T]GAGTAATTTTTTTAT	23077
rs565417531	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77268051	AATACATCAATATTG[A/G]TGTCTAAAAGATATT	23077
rs565419575	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77230767	ATGGAAAAGCTTTAT[C/G]ATAGCTGAAGAGGGC	23077
rs565433829	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77269809	GGGCCAGAACTAAAA[C/T]TGAACCTCTTATGAG	23077
rs565436492	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77218453	CACAGTATCATGAGA[C/G]GCATTAGAGCAGTGA	23077
rs565448127	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77321720	GCCATGCCTTTGTCA[C/T]AGTAGGTTATACTTT	23077
rs565450990	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77244458	GGGAAAACTGGCTAG[A/T]CATATGCAGAAAACT	23077
rs565454396	snp	A/T	1.66751e-05	0.00288744	synonymous-codon	MYCBP2	GRCh38.p7	13:77056992	TTTCCATACCTTGCA[A/T]ATGGGACAAGATATA	23077
rs565456657	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77057995	GGCACCCACCACCAC[A/G]CCCAGCTAATTTTTT	23077
rs565469075	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77207925	TAAGAGACAAGAAGA[C/T]ACTAGAAATTATCTG	23077
rs565480654	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77323564	TTGCCCTATCACATG[-/A]AATAGGTTTTATTGC	23077
rs565495583	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77214357	TATTCACTACTACCA[C/T]TACAAAGTATTGGAA	23077
rs565510600	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77245452	GAGTTCGTGTTCTTT[G/T]CAGGGACATGAATGA	23077
rs565535381	snp	A/C	0.000399281	0.0141238	intron-variant, missense	MYCBP2	GRCh38.p7	13:77129198	TGAAAATACGTCCAA[A/C]TCCCTGACTCCTTGG	23077
rs565548022	in-del	-/AAG	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77110979	TTCTTAAATAAACCA[-/AAG]GAGGAAAGACAATCT	23077
rs565563516	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77208582	TGGAAAGATCTCTAA[A/G]TTATTTTTGAGCAAA	23077
rs565565904	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77237621	TTGACCTAAATTCCT[A/G]TATTACTTTAATATG	23077
rs565566330	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77107062	AAATCTAATTCTATA[A/G]ATCTGTCACAAACAA	23077
rs565572970	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77316453	TAGCCAACCAATGTT[C/T]CCAGCAGTCGTGGGG	23077
rs565577429	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77251515	AAATTTTAATTTAGG[C/G]ACCACTAATAAACAC	23077
rs565604809	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77094174	GCTACACAAAGAGGA[C/G]AATTTCCAAAATGGA	23077
rs565624677	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77252211	AGAAATCAGCAAACC[G/T]TTTATAAAGAGCCAG	23077
rs565665084	snp	A/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77152130	GTTCTTAACAACGCG[A/T]TTCTATGGAATCAGT	23077
rs565670105	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77120241	TACACTATGTAAGTA[C/T]AAAGATCTAGCTTAA	23077
rs565683920	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087861	TCATGGCTCACTGCA[A/G]CCTCAAGCACCCAGG	23077
rs565694360	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77080313	CCACTGTGGCTCTTC[A/C]TGAGAAAGGAAATAT	23077
rs565704531	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77173169	TATTTAAAACTAAAG[A/G]ACTTTAACATTTTTC	23077
rs565705135	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77269308	GTAAGAAACCCTAAT[C/T]TGGCCTCAGGACATG	23077
rs565707347	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77159848	CTAATAGAAACTCTT[G/T]GATAGTTCTCCTTCA	23077
rs565727860	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77137248	CTTTAAAATAAAATC[A/G]TGGGATTCAGAATTG	23077
rs565729261	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77151528	ATTTGATTTAAGCAA[C/T]CTATTAAATAATTAA	23077
rs565732849	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77138138	GTTCAACTTAACCTC[C/T]GTAAAGCAGTAAGCC	23077
rs565736560	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77229195	TAGCTTTCCTATCTA[C/T]AATATAGCAACAATG	23077
rs565750130	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77088304	CAAAGTGTATCTCAA[C/G]CTCTAGGCAAGCAAC	23077
rs565767719	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77185065	AGTATTAAGCAATAT[A/G]TCAGATTTTCAACTA	23077
rs565774936	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77189447	TACAAACAGTAACTA[C/T]AACAGATTGCACGGT	23077
rs565788285	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77312505	CTGTGTTTTAAGTGA[A/G]TTAGTATAATAATAA	23077
rs565792205	snp	C/T	1.6477e-05	0.00287024	synonymous-codon	MYCBP2	GRCh38.p7	13:77144485	ATGAAGAGTGTAGAG[C/T]CCAATAGCCCCTGGA	23077
rs565798427	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77197811	AAAAAAAGACTGACT[A/G]CTGTTGAAAGGCCTT	23077
rs565847278	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77160326	GGCGAACTGCCTAAA[C/T]GCTCTATGCCTCATT	23077
rs565854970	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77243544	CTTGAACCTAGAAGG[C/T]GGAGGTTGCAGTGAG	23077
rs565885414	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77181610	AGCTTGGTGTGTTTA[C/T]AGTTTTATTGCCTCT	23077
rs565887299	snp	A/C	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77190077	TATGGAAAATGTTTA[A/C]AAATATACAAAATAT	23077
rs565902996	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77260897	TCTCTAAATTAGCTA[C/T]TGCATTATTAATACC	23077
rs565909527	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77298964	TGGTCAATAAATATC[A/T]GATGAACAAATAAAT	23077
rs565911247	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77222013	GTTGTTTAGGAAATA[A/C]TAACAAGACAAAAAC	23077
rs565943226	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77173789	AGGGTTGTTATCATT[C/G]TTTTATTTTCCAAGG	23077
rs565948956	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77303651	TAGTCACAATGGAAA[A/T]CAGAAAATATTTTCC	23077
rs565950126	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77250549	GATTCAAAATTCTTC[C/T]TAACATCCTAGCAGA	23077
rs565977683	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77064256	GGTCTTGTCTCCAAA[G/T]GACCTTCGGTCTATC	23077
rs565981697	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77153461	CCTGTCTCAAACATA[C/T]TTGATATTAAATTAC	23077
rs565992526	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77282951	ATAATTCCAACCCTC[A/G]TTAACACTCTCTAGA	23077
rs566019918	snp	A/T	0.000798403	0.0199641	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77328673	CTAAGGCCTGACAGG[A/T]AAGCAATGAGAGGGC	23077
rs566038402	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77321035	TTGACTGTGGTGATA[A/G]TTTCAGGACTCTTCA	23077
rs566050404	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77221642	TTATCTAACTGCAAT[A/G]CACCTTTCCCAGTTT	23077
rs566055771	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77146847	TTTGGCAATACTTAA[C/T]GTAGTTGTAGTTGTG	23077
rs566065000	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77213932	CACCCACCGGCTACT[A/G]CAAACCTGAGCATGT	23077
rs566068330	snp	A/G	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77284334	GAACAAAGAAAAGGA[A/G]CAAACTAGGATAATA	23077
rs566072342	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77112731	GGTGTGAGCCACTAC[A/G]CCTGGTCTGCATCCC	23077
rs566081821	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77281794	TTCATGACTAAGTGT[A/G]ATCATAAAAGTTTAG	23077
rs566091790	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77255187	TCATACGAATGAAAA[A/T]TCTATGTTTTCCATA	23077
rs566096677	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77272469	ATCCTATTAAAATCT[C/G]GTATATGGTATCTGA	23077
rs566106500	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77162915	CCACCTTGGCCTCAC[A/G]AAGTGCTGGGATTAC	23077
rs566115888	snp	A/C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77065448	ATACTATCTTGTCCT[A/C/T]CTCAGGCTGCCCTCC	23077
rs566131857	snp	A/T			utr-variant-3-prime	MYCBP2	GRCh38.p7	13:77044715	ATGTACATTCCAATA[A/T]GTTTACAGCTGCAAG	23077
rs566134854	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77271609	TGTTCTCATGATAGC[A/G]AATAAGCCTCACGAG	23077
rs566151959	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77306774	CAACAAGAGGAATGA[C/G]AGCAAGCAAATAACT	23077
rs566186297	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77313677	AGAACGAGAAGACAA[G/T]GCACAGATTGAAAGA	23077
rs566187275	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77102010	GATAATATGCAAACA[C/T]TTTTCTAACTTTAAA	23077
rs566188626	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77050413	TCTCACTTCCGTGAA[A/G]CCTGGTATTCCACCT	23077
rs566200573	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77139796	ATTTTCAGTGAATAC[A/C]TGTACAGGTTCTGAA	23077
rs566226135	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77206921	AAAGAGAATAAATAA[C/T]ATAGTCAGCTTAAAG	23077
rs566233369	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77192886	GTAATCCCAGCACTT[C/T]CAGAGGCCAAGGCAG	23077
rs566239129	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77155840	AGTCCCCGTAACAGG[C/T]AGCAAAATGTAAAGA	23077
rs566241299	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77163615	ACAAATTTGCTCCAT[A/G]TAAAAAAGTACCATT	23077
rs566267030	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77159633	TACAATATCTGGTTG[C/T]TTGATAAGTGTGTAG	23077
rs566273681	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77199692	GCACACAGCTGGAGA[C/T]CTGAGAAAGGGCAGA	23077
rs566279221	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77199166	TGCCAGACAGTGGGA[G/T]CAGGACAGTGGGTGT	23077
rs566284842	snp	C/T	0.000207351	0.01018	missense	MYCBP2	GRCh38.p7	13:77097546	TCCTTTTTGGACTTC[C/T]TATTCTCTTTCTCAC	23077
rs566303164	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77302270	CATGGTCATATTGCT[A/G]AAAGCAAAGCATAAA	23077
rs566308888	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77321732	TCATAGTAGGTTATA[C/T]TTTCTTGGTCATTTC	23077
rs566342548	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77281963	TACCATAGAGTGAAG[A/T]ATACTGTCTTTTAAA	23077
rs566346989	snp	C/G	3.29641e-05	0.00405968	missense, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081479	TAGCGGGCATTGATT[C/G]CTTTTACACAGTTGA	23077
rs566360487	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77128366	AAGCAAATATCCATA[A/G]ATTTAGCAAAAAAAC	23077
rs566360709	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77091385	AGAGGAAGTTTTCTA[C/T]TAACTTAAAAAAAAT	23077
rs566380706	snp	A/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77169926	AAGATACTTTTATTA[A/T]CCCCAATTTTCAGAA	23077
rs566388539	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77078043	AAGAAATGACCTGGC[A/G]ATTTCTATGTGATTT	23077
rs566391415	snp	C/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77238843	TAGTACAAGAACTAG[C/G]GCCCAGGCCGAGCGC	23077
rs566391900	snp	C/T	3.33461e-05	0.00408313	synonymous-codon	MYCBP2	GRCh38.p7	13:77191732	ACAGTCACTGCTGGG[C/T]CCTGACACTCGGGCC	23077
rs566421024	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77187291	CAAAAGATACCAAAC[G/T]CAACTTAAGACTAAT	23077
rs566423592	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77265013	AATTCTGATTTTGAA[A/G]TGCAGTAATGGAGCC	23077
rs566424673	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77316652	GGAAAGTGGGTCAAA[C/T]CACAGCCCCAGCCAC	23077
rs566426888	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77295402	CTCCCAAAGTGCGGG[G/T]ATTACAGGCGTGAGC	23077
rs566432392	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77325301	TAACAGTAAACTCTT[C/T]AACTCATTTTGACAG	23077
rs566436956	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77170703	TGCCTCAGCCTTCTG[A/T]GTAGCTAGGATTACA	23077
rs566447657	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77046207	ATTAATGTGCTTCAC[A/G]TCATGGGTTTCATAT	23077
rs566448738	snp	A/C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77236471	TTGATCTAGTAACTG[A/C/T]ACCCTAGGAATCTAT	23077
rs566477820	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77108928	CAGGATGGTCGACCT[C/T]GTGATTCACCCGCCT	23077
rs566494049	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77179868	GTGGTGGGCTTGTGC[A/G]ATGGGGCAGATGACG	23077
rs566496810	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77317188	AACTCCTGACTTCAC[A/G]TGATCCACTCATCTC	23077
rs566516986	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77201409	AAGTCCTGAGTGACC[C/T]ACAAAGAGACTTAGA	23077
rs566529314	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77187877	TCAGGGGTTCGAGAC[C/T]ACCACCAACATGGTG	23077
rs566533898	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77150114	TGAAGATAACTAAAA[C/T]ATCCAAAATATATAT	23077
rs566567752	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77202146	GATAGACCGCTAACA[A/C]GACTAATAAAGAAAA	23077
rs566568306	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77061000	TGACTTTTGGTCTAA[C/T]GCTCTCTTCACCATA	23077
rs566570658	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77232174	GATTATACTATATTG[C/T]CTATGAAATTTTTTT	23077
rs566572729	snp	C/T	0.000940359	0.0216632	intron-variant	MYCBP2	GRCh38.p7	13:77273681	ACTCTGTGGATAAAA[C/T]AGAATTCAATTATAT	23077
rs566590164	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77257558	TTTAAATAGGAACAA[A/G]AAGAAAAAGAAGAGC	23077
rs566590739	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77117029	TTTTCTACCTGACTG[A/T]TCCTGATATTTTTCC	23077
rs566598912	snp	C/T			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77292567	ATATGATCACATTTA[C/T]ATGAAGTTCTAGAAA	23077
rs566611123	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77218047	CAACAAGGAGTAGGA[A/G]AGATAAAAGGCACTC	23077
rs566611609	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77309576	CTCCCTTTCTATCTA[A/G]ATGAAAATCATTATT	23077
rs566621798	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77249812	AATTTAAAAATAAAG[A/T]AGTTAGGTGCTTAAA	23077
rs566629667	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77174638	TTAATGAATCAAACA[C/T]GATGACGGCTAACAT	23077
rs566635185	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77086031	AGATACATATCCAGG[A/G]TTGATCTTTTATCAT	23077
rs566680690	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77101615	GGTGAATATTTTCTT[A/T]AGATCTGTAAGTGGT	23077
rs566683508	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77195615	ATAGTCCGAAATAAT[A/C]ATTTTTCCATATTTC	23077
rs566699126	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77219734	GAGATCCTATGCTAA[A/T]AGGAGGAAACAGGTG	23077
rs566704377	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77053254	CTTGCATAAATAGAA[A/T]TTGAATAAATAAAAT	23077
rs566711732	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77147201	ATTTGTATTCAGTAA[A/G]AGCCTAAAAATATAT	23077
rs566713033	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77287129	CCTGACCTCGTGATC[C/T]GCCCGCCTTGGCCTC	23077
rs566730336	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77134794	ACAGTTAAAGTCACT[C/T]TGAACTAAATTAGGA	23077
rs566743583	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77327069	ACCACCGCCACCACC[G/T]CCGGGGCTACCCGCA	23077
rs566750146	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77323682	TATCTTGCTCACCGC[C/T]ACATCTTCAGCATCT	23077
rs566756295	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77062084	ATATCTAAACATTCT[C/G]TATGCCAAAGGAAGA	23077
rs566773940	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77171230	AAGAATAAAGACCCA[G/T]TTTAACTCAAATACA	23077
rs566775179	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77275970	GCCTGGGCAACAGAG[C/T]GAGACTCCGTCTCAA	23077
rs566775819	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076972	TAATATACACCACTA[C/T]TTTTCTTAATTACAA	23077
rs566781659	snp	C/T	1.64871e-05	0.00287111	missense	MYCBP2	GRCh38.p7	13:77150742	AAATTACCTTCATCA[C/T]TGTTATGGCAATATA	23077
rs566783767	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77202472	CCAGAGATACAAGGA[G/T]GAACTGGTACCATTC	23077
rs566787270	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77250645	GAAAAATGTGGTCCA[C/T]TGAGAACAAGGATAA	23077
rs566792909	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77103653	TCATTTAAATAAAGA[C/T]TTACAAGTTTTTTTT	23077
rs566817880	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77093821	GTAGGAACATACATA[A/G]GATCATATTTGAAAA	23077
rs566829386	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77153676	TTTTACAAACTGTGT[G/T]ACTTAAAAAAAAAGT	23077
rs566834950	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77297950	CATACCCTTCAATCC[A/G]TTCTTCACATAGGAA	23077
rs566837466	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77170348	GATAAGCTGAGCCTA[C/T]ACTGTGAAGACCTTT	23077
rs566850751	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77135323	AACTGAAGTAAGAAG[A/G]GAGAAAGATAGTTTT	23077
rs566851999	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77226754	CTTTCCTTTCCGTAA[C/G]TAAATGCCTATAATT	23077
rs566864540	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77212417	TGAAATATTTTCCAC[A/G]CAAGAAGTATCTCCA	23077
rs566865615	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77181402	ACTTACCTTCAAATG[G/T]TTCAGGAAAAACAAA	23077
rs566871569	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77319464	TGCTACCCTTAAAAT[A/T]AAGTTTTGGGTTGAA	23077
rs566882503	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77086699	ATTTGTTTGCTGACA[G/T]GCTATAAAATGTCCA	23077
rs566882698	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77280438	AGAAATGTGAAGTCA[A/C]AGATCTCCAGAGTAC	23077
rs566925420	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77265469	ATCTGTAAGATAAGC[C/T]GAGGTTTAAAGAATA	23077
rs566926091	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77127983	ATTTTATTTACCAAT[A/T]TTCTTTGGTTACATA	23077
rs566942638	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77119022	AGTTATAAATTAATA[C/T]TTTCTTTTTTAAGTT	23077
rs566947047	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77110303	GTGTCTGTCTTATTC[A/G]GTTGAGATAAGGACT	23077
rs566977565	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77151140	TTGACAATATGAACC[A/C]TGAACACGGTGTAAA	23077
rs567004768	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77205069	TAAATAAATAAATTT[A/T]AAAAATTTAGTATTA	23077
rs567015225	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77178403	TCTTCAACCAGACTA[C/T]GTCCTCTCTCCTCTT	23077
rs567021980	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77210399	GGGTTTCACTGTGTT[A/G]GCCAGGATGGTCTCG	23077
rs567029279	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77259070	GACCAGCCTGGCCAA[C/T]ACAGTGAAACCTCGT	23077
rs567030823	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77150210	ATTTGAGAGAACCCA[A/G]AATTGAAGGGGGCAT	23077
rs567036541	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77162849	TTTAGTAGAGACGGG[A/G]TTTCACTGTGTTAGC	23077
rs567038262	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77267382	TCTCTGTCTCTGAAA[C/T]CCCTTTAACATAAAA	23077
rs567076915	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77274288	AAGATGAAACACACA[C/T]ACACACAAATGTTTT	23077
rs567076969	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77266412	TTTAATGACCTAGAA[A/G]TATTTTCAGAATATT	23077
rs567094253	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77172184	GATTATAGGAGTGAG[A/C]CGCGCACCCAGCTGA	23077
rs567110133	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77143263	CCAGACAAGACTGGC[A/G]TGTGAGTGTGAGTGG	23077
rs567128111	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77312037	AGGGGAATAAGGTTT[A/C]CATTACAAAGATTTT	23077
rs567159865	snp	C/T	0.00636936	0.0560724	intron-variant	MYCBP2	GRCh38.p7	13:77107691	TGCAGTGAGCCTAGA[C/T]TGCACCACTGTACTC	23077
rs567181769	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77158201	ACTTTCAGATAGGCC[C/T]TTACGGAGAAATCAT	23077
rs567208443	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77239386	ACTAACATTTTATTT[C/G]ATGTTTCTATTCCTC	23077
rs567217140	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77310196	AGCAATACAGGGAAC[A/C]TAATAACCTAGTCCT	23077
rs567222352	snp	C/G	4.02544e-05	0.00448615	intron-variant	MYCBP2	GRCh38.p7	13:77288412	TTTCCATTTCACACT[C/G]TTTTCTATCATCAAG	23077
rs567236676	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77296215	GCTTGAGCCCACGAG[C/T]TCGAGACAAGCCTGG	23077
rs567239355	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77218864	ATGTAATTATGACAC[C/T]TTAAATTTTAAAAAT	23077
rs567242787	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77143904	ATAGAAAAGGTACAG[A/G]AAAATCTTATAGGAC	23077
rs567245380	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77053495	GCAGAGGTTATAAAC[A/G]GTCGTTCACCAGCTA	23077
rs567250401	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77310693	CAAAATTTGCAAGTT[A/T]AATAAAAATTGACAT	23077
rs567256125	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77273301	TTAAAGCTTCAGAGT[C/T]AAACATACATATCAC	23077
rs567258801	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77287666	CAGAAAGGAAAAGGC[A/T]CTCAGCCCTGCTACT	23077
rs567291314	snp	G/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77101747	TTATTTTTCCAAAAC[G/T]TATTTTATATATTAA	23077
rs567291894	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77172279	GGAACATACTGGTGA[A/C]TTAAAGGAACAGAAT	23077
rs567299483	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77192185	AAATAGTTTTGAAAG[C/G]CAGCATATTAAGAAA	23077
rs567304871	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77242979	TACCAAATTAGTTTA[C/T]TGTGTGAACTTTTCA	23077
rs567306497	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77061052	AATATATAGATCAAT[C/G]ATGTCATAATTAAAC	23077
rs567329103	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77180648	CTTTTTTGGCTGGGC[A/G]TGGTGTCAGCAATAC	23077
rs567329993	snp	A/G	4.95372e-05	0.00497656	synonymous-codon	MYCBP2	GRCh38.p7	13:77165371	CTGATGCAGTCTCCA[A/G]TGAAAAAAGGGCCTC	23077
rs567330724	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77202663	AAATACTGGCAAAAC[A/G]AATCCAGCAGCACAT	23077
rs567362913	snp	A/T			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77227791	AAATATAGGCATAAA[A/T]CCCACAATAGAGACA	23077
rs567362991	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77157492	GCCTCCTAAAGTGCT[C/G]GGATTACAGGCATGA	23077
rs567368715	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77195155	TCTAAATTTTTAAAT[C/T]ATATGCTAATGACTT	23077
rs567389022	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77250764	ATCTAATCAAGTACT[C/T]TTTATGATATCGATA	23077
rs567402593	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77319613	TGTTATTTACCAAAA[C/G]CCATCTGATGATTGT	23077
rs567404415	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77172860	GAAATCTGACTTCCT[A/G]CCTACAAGTCGCAGT	23077
rs567408976	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77232613	AAAGTCTTCATGATT[C/T]GTGCTTTGCTTGCAC	23077
rs567411586	snp	A/G	1.64798e-05	0.00287047	missense	MYCBP2	GRCh38.p7	13:77251337	TCCATTGCTGTTGCC[A/G]TATTTTCAACTCCAA	23077
rs567418444	snp	A/C	0.00597247	0.0543191	intron-variant	MYCBP2	GRCh38.p7	13:77202190	TCAAATAGACGCAAT[A/C]AAAAATGATAAAGGG	23077
rs567420622	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77223252	GTTGGTCTATTCCTG[A/C]CCAATGCAGGACCCT	23077
rs567422809	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77063399	CCAGTCTTTACTAAA[C/T]ACAAAAAAAATTAGC	23077
rs567424467	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77086806	ATTCTCTTATATTTA[A/G]CCAATTTTTTCACTG	23077
rs567447484	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77259759	GAAACTCAAAGGCTT[G/T]ACATATTTATCACAC	23077
rs567447568	snp	C/G			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228437	ACCTGAGCCCGGGAG[C/G]TCAAGGCTGCAGTGA	23077
rs567463961	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77319077	TTTGTGTCTGTGGTG[A/G]TGCTTTGGGGTGCCT	23077
rs567486580	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77094550	ATTACTTGGGTGAAC[C/G]AATCACTTTGAACGG	23077
rs567487530	snp	A/C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77312485	TCTGTAGGGTTGCAA[A/C/G]GTTTCTGTGTTTTAA	23077
rs567496054	snp	C/T	1.65222e-05	0.00287417	missense	MYCBP2	GRCh38.p7	13:77055578	TGCATTTGTAGCACA[C/T]ATAATATGCATATCT	23077
rs567499901	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77327116	CTCACAGAGCATGCG[C/G]CACTCCTCGCACATG	23077
rs567504707	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77322898	TCATTCATCCAAAAA[C/T]ATATCTATTCAGTCA	23077
rs567525584	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77274399	CCATAGAACGGAGAC[C/T]TGAAAATCCTTATAG	23077
rs567548632	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77188418	CATACGTAAGAATCC[G/T]CAATTAATACATGAG	23077
rs567557797	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77221560	TCTGGCAAGACCATG[A/T]AATACTATTTGCCAA	23077
rs567559739	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77063930	CGCCCTAGGGATATA[A/T]AGTTTATCTTCTTCA	23077
rs567582378	snp	C/G	0.000399281	0.0141238	missense	MYCBP2	GRCh38.p7	13:77206693	TCGGGTAGTGAGGGC[C/G]CTTGATCCTGTTGGT	23077
rs567591917	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77249956	TGGCCGGGCGCGGTG[C/G]CTCACGCCTGTAATC	23077
rs567601071	snp	A/G	0.00597247	0.0543191	intron-variant	MYCBP2	GRCh38.p7	13:77071917	AACCAGAAATTAATA[A/G]TATAAAGCTAACAGG	23077
rs567619417	in-del	-/A	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77140525	AAAATGCCTGTACTT[-/A]CTCTTTAGATTTCAG	23077
rs567621073	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77313496	CTCAAAATGGAAAAC[A/G]GACTTTATATGTAAA	23077
rs567623749	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77212506	TAAAATATTAGTATT[C/T]CAAATTGTTCATTTA	23077
rs567639523	snp	A/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77047634	AGGCACCGATGAGGG[A/T]ACTAGCACAGGGCAT	23077
rs567661912	snp	C/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77205968	ATCAACACTAGTTTT[C/G]GATGTCTACAATAGA	23077
rs567693653	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77236567	CATTATAGCAACATT[C/T]TAAAAATACCCAAAT	23077
rs567723591	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77184103	CACTGATTTTAAACC[C/T]TTCTTCTTCATATAA	23077
rs567736242	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77119810	GCAGACTACATCCTT[A/C]AACTCCTGGCCTCAA	23077
rs567769682	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228951	CATATAACAGAAACT[A/G]CCACAGAACACAGTG	23077
rs567785285	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77327720	AATATTTTTTAAATT[A/G]CTCTTTTTTATTGAC	23077
rs567796528	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77119353	AAATAGTATCTTTCT[A/C]GTCATATTTCTGAAA	23077
rs567813322	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77066808	CATTTCTCTGATTAG[G/T]AGTGAGGTGTTTTCA	23077
rs567830284	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77213181	ATAAGAGAGCACAAA[A/C]ATGTAAACAGGGGCC	23077
rs567834616	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77049033	TCATATGGCTACAAC[A/G]TGTGACTGATTTTTC	23077
rs567843854	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77242604	AACTGGAGGGCAGCA[C/T]AGCAGGACTATGTCC	23077
rs567848361	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77273824	TTACTCTCTTCCCCA[A/G]AAGTTAAAATATTTA	23077
rs567855198	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77297568	AGTAACAGCAGTGAC[A/G]AAAGAGAAAAATTTT	23077
rs567860852	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77286921	ATGGAGTCTAGCTCT[C/G]TTGTCCAGGCTGGAG	23077
rs567879445	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77165915	TTAAAACATAGTTTC[A/T]CTTCACACAAGAAAG	23077
rs567884943	snp	G/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77252410	AAGCTTATAATGTAG[G/T]AAGAAAGACAGACAT	23077
rs567886603	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77058934	AGGTTGCAGTGAGCC[A/G]AGATCGTGCCACTGT	23077
rs567906406	snp	A/C	1.66219e-05	0.00288283	intron-variant	MYCBP2	GRCh38.p7	13:77267820	TTGCTTGTGGAGAAA[A/C]AATGACTACTTGAAA	23077
rs567925760	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77096099	GCATATGTAGCAGAG[A/G]TTATCTAGTGTTATT	23077
rs567938574	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77260676	AAAGCTAAAAAAAAA[A/C]CCCATATTATTTGCA	23077
rs567951772	snp	C/G	4.94181e-05	0.00497057	synonymous-codon	MYCBP2	GRCh38.p7	13:77067658	TGTTCCAGTGATGGT[C/G]GTTCCTTTGGCTTTT	23077
rs567964983	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77152201	TGACAAATATGTTCC[A/G]TTAAGTGACCACTAT	23077
rs567974294	snp	C/T	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77210349	AGGTGCCCGCCACCA[C/T]GCCCGGCTAATTTTT	23077
rs567995018	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77099625	CCTGAAGCTGTTATT[C/T]AATTATTTATAAACA	23077
rs568013287	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77289671	AGCAACTCATCAACA[G/T]TGTACTGGATATCCT	23077
rs568017501	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77153371	CATCCTGCAAGGGGT[C/T]TGAGTGCAGCAGTCA	23077
rs568018121	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77095869	TGTAATTCATTTTTT[A/T]AAAAAGTAAATCATT	23077
rs568036485	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77223879	GAAAGGGAATCTTTA[C/G]CTGCACGATCATGTC	23077
rs568046585	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77166844	TCCTAAAATCTAAGA[C/T]AAAATAAATGACTCT	23077
rs568061415	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77209954	GCTGTCTGATGAGAA[C/T]GCAAGCAGGCATGGG	23077
rs568067530	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77093084	GATGTATTAAAGAAC[G/T]TCTACAGGACTCTTT	23077
rs568089092	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77239297	TAATTATTAACATAC[C/T]ACTAAATTTTTAGTT	23077
rs568119004	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77114414	AAAATTCAGACCTGT[C/T]AGATAACTTAGAGAG	23077
rs568135482	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77057904	GTGCAGTGGTGCCAT[C/T]TCAGATCACTGCAAG	23077
rs568138193	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77201073	TAAATGGACTAAATG[C/T]TCCAATTAAAAGACA	23077
rs568151652	snp	C/T	0.00121744	0.0246422	intron-variant	MYCBP2	GRCh38.p7	13:77270256	AATTCATTATGGTTA[C/T]AACTCTGTATAATTA	23077
rs568157392	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77223072	TCCTGTTTCCATGGT[A/G]AGACAACCACAGACA	23077
rs568167418	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77148741	AAATCTTTTCTGATC[A/G]GTGCTTTCTTTTAAT	23077
rs568172259	snp	C/T	3.2963e-05	0.00405961	synonymous-codon, intron-variant	MYCBP2	GRCh38.p7	13:77233172	TTTGTGCTTGTCCCG[C/T]TTATGCTTTAGCTGT	23077
rs568192067	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77143940	TTATATACGCTGTTC[A/G]TCACTGACCAAAATG	23077
rs568228884	snp	C/G	1.86775e-05	0.00305588	intron-variant	MYCBP2	GRCh38.p7	13:77263631	AAAATATAGGGAAAA[C/G]ACTTAATTTGCTATC	23077
rs568249570	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77053249	AGACACTTGCATAAA[C/T]AGAATTTGAATAAAT	23077
rs568263432	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77271071	GTCTGACTACTTTTT[A/G]TATTCTCACTACTTA	23077
rs568277174	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77161503	CACCAACTGTACCAA[C/T]CTCACCTTTTGCTGC	23077
rs568305591	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77235015	CTAAAAATTAAAGCA[A/G]TTGGGCTCGAAAATA	23077
rs568306251	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77108407	TTAGGCCTTAGAAAG[A/G]ATAACTTCAAAATAT	23077
rs568314216	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77125122	TGAGTCTATATGTTT[C/T]GAATTTTCTTTTAAT	23077
rs568318051	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77248952	AAGCAAAGATGTTCC[C/G]ACATATGTGACAACC	23077
rs568333405	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77300856	AAGAACAAAAAATCC[A/G]GAGGTGGAAGAGCAC	23077
rs568345547	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77117842	AAGGACTAGAGCAAT[C/G]CTAAAAGACAGAACT	23077
rs568349218	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77234350	AACAAGTTTTTTCAT[C/G]ATTCTCTATTGATCT	23077
rs568369510	snp	A/G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77154968	ATGTATGTGTGTATG[A/G/T]ATATATAAAGTATAT	23077
rs568383305	in-del	-/TGCCTTGTGATCTTTGCTTTGCCCTT			intron-variant	MYCBP2	GRCh38.p7	13:77110503	TTTAATTTTGCCCTC[-/TGCCTTGTGATCTTTGCTTTGCCCTT]TGCCTTGTGATCTTT	23077
rs568390207	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77063035	AATATTTACTACTAA[C/T]GTCTTCTGAATATTT	23077
rs568401434	in-del	-/A	0.152334	0.230133	intron-variant	MYCBP2	GRCh38.p7	13:77134582	AACAACAAAAATAAC[-/A]AAAAAAAAAAAGGAA	23077
rs568406550	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77256833	GTATGGAGCTTCCCC[A/C]AAAAACTGAAACTAG	23077
rs568414335	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	MYCBP2	GRCh38.p7	13:77044320	AGCTGAGATCACGCC[A/G]CTGTACTCCAGCCTG	23077
rs568415044	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77280348	ACATTTGATATAGTT[C/T]CTTTTCCTGGAATGG	23077
rs568424805	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77097029	TTGCAATTCTGAACA[A/G]GAAAATAGTAAAATC	23077
rs568427878	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77247616	GACCTCAAATAGCCA[A/G]ACAATCTTGAAAAAG	23077
rs568429429	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77066966	TTGTAGTCATACTTC[A/T]ATATTATGCTAACAA	23077
rs568448443	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77125732	TAATTTTAAGAATTA[C/T]CCAAGAACACATGGC	23077
rs568458764	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77128361	TAAAAAAGCAAATAT[C/G]CATAGATTTAGCAAA	23077
rs568467175	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77169224	CCACGGTGAAACCCC[A/G]TCTCTACTAAAAATA	23077
rs568469926	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77101372	ACCTGCACAACAGCT[A/G]CATGCAAAGGAATGG	23077
rs568482914	snp	A/G	0.011928	0.0763002	intron-variant	MYCBP2	GRCh38.p7	13:77248153	TAATCAAAAAAAAAA[A/G]AAGAAGAAGAAAAGA	23077
rs568484864	snp	C/T	0.00398564	0.0444627	intron-variant	MYCBP2	GRCh38.p7	13:77217040	GGATCAAAATGTTAA[C/T]AATAGGTGAATCTGG	23077
rs568485913	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77141766	ACAGAGTGAGACTCT[A/G]TCTCAAAAAAAAAAA	23077
rs568486477	snp	A/C	1.66012e-05	0.00288103	missense, utr-variant-5-prime	MYCBP2	GRCh38.p7	13:77278859	AGGGATGGATGAGAA[A/C]ATCGTGTCTCTTTGA	23077
rs568493763	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77194953	AAAACAGAAAAGATA[A/T]CCAATACAAAAAGGT	23077
rs568520615	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77278364	GCTTCATCATACTAA[C/T]TGAGAAATGTGTGTG	23077
rs568567221	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77286232	GTAGTAAAAAATATT[C/T]ACACAATCCCTTGTG	23077
rs568567346	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77294697	ATAGAGGTTGGAATG[A/G]CTGTATTTGTTAGAG	23077
rs568569269	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77128074	AATAAATGTAAAATA[C/T]GCATTTTATATACTC	23077
rs568581891	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77293611	GGATTTTGAAATGCA[C/T]AGATTATCTGGATGG	23077
rs568587349	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076235	AAGACAAATTAGACA[C/T]GGACTTGGTCTTTAA	23077
rs568589845	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77316534	GGATTCACTATATTT[C/T]GCCTATTATACAATT	23077
rs568601798	snp	A/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77162044	TCATTACACTTTTTT[A/T]AAAAAAATAATTCTG	23077
rs568603722	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77169770	GGTAATTTCATTGTA[C/T]TGCATACATGCTGTA	23077
rs568615646	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77058979	GACACAGCCAGACTC[C/T]GTCTCAAAAAAATAA	23077
rs568625788	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77170107	ATCAGTGACATTAGG[C/T]AAATTACTTACTCTG	23077
rs568633270	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77134570	CAAAACAAAAAACAA[C/T]AACAAAAATAACAAA	23077
rs568633511	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77218263	CTGGTACTCTGTATA[C/T]TGACTGGCCTGTTAG	23077
rs568635107	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77224903	ACAATTACGTACAAC[A/T]TCAATGAAACAGCAG	23077
rs568641875	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77176261	ATCCAAAGCTAAGTC[C/T]GTTTGACTACAAAAC	23077
rs568643457	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77187032	CCTGGCTGGTCTTGA[A/G]CTCCTGAGCTCAAGC	23077
rs568649588	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77278997	GGTACAAGTTACTTC[C/T]ACAGCAAATGATAAT	23077
rs568649832	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77272712	AAGGGAATGGGTCTT[G/T]TTTGACCAGGAGAGT	23077
rs568657231	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77315620	TATCAGCAAGCCGGG[G/T]GCGATGGCTCACGCC	23077
rs568670212	snp	C/T	6.61365e-05	0.00575012	intron-variant	MYCBP2	GRCh38.p7	13:77225574	AAGTGTTATAATTTG[C/T]GAATTATGATTAAGC	23077
rs568677087	snp	A/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77178051	AATAACCTTTATTTA[A/T]TAAGTGGATATAAAC	23077
rs568678340	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77184788	ACAGATGAGGGTGGC[A/G]GGGGCCTCCTGGTGC	23077
rs568683213	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77286970	GCTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAC	23077
rs568686623	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77279678	CAGTGGAAGAATATT[A/C]TCTCTGCTGATATTT	23077
rs568713662	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77159098	AATTTGAAATTATAC[A/G]GTTTCAAAAATAATC	23077
rs568741358	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77162817	ATGTGCCACCATGCC[C/T]GGCTAATTTTTGTAT	23077
rs568749136	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77124308	AGATATCTCCAAAGA[C/T]ACTCCATCATTATTG	23077
rs568750274	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326359	AGAGCGGACTGAAAG[C/G]TCAATAAATGCGCAG	23077
rs568751882	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77052058	CCCTTGAAATGCCAA[A/G]TGCATGCCCATATTG	23077
rs568764388	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77170736	CACCTGCCACCACGC[C/T]TGGCTAATTTTTTTA	23077
rs568771340	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77177089	TTCACTAAGAATCAC[C/T]CATTAGTACTCTATG	23077
rs568779539	in-del	-/AAATAAATAAATAAATAAATAACAGAATTCAATC	0.00557542	0.0525036	intron-variant	MYCBP2	GRCh38.p7	13:77301981	TTGCAAACAGGCCAA[lengthTooLong]ACGGAAACAAAAATG	23077
rs568795477	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77323169	AAAAACTGAGGCATA[A/G]AAGTTATGTAATATA	23077
rs568805605	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77271141	CTTTATATATTCATA[A/C]ACATACACATTCTAT	23077
rs568808333	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77113447	TGCTCATCACCATAA[C/T]CTAGCACAGAGTAGA	23077
rs568841719	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77260679	GCTAAAAAAAAAACC[C/T]ATATTATTTGCATTT	23077
rs568841774	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77292454	ATGTATATAAAATCA[C/G]CAAAAAAATGGAATG	23077
rs568845280	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77271502	ATATGGTTTGGTTGT[A/G]TTCCCACTCAAATCT	23077
rs568851609	snp	A/C	0.154661	0.231107	intron-variant	MYCBP2	GRCh38.p7	13:77223910	ACGAACTAAAACTAA[A/C]ACTAAAACAAATGAA	23077
rs568861482	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77108894	ATTTTTAGTAGAGAC[A/G]GGGTTTCACTGTGTT	23077
rs568866595	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076405	CATGAAGAGGATAAA[C/T]CGTAAAAAAGTTTCA	23077
rs568878433	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77289648	TCCAGGCAAATTGGT[C/T]TACTCTCAGCAACTC	23077
rs568889379	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77210074	AAAAGGAAAGAAGTG[C/T]TCAGCCCTGTGATGA	23077
rs568900160	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77323943	ACCTCTTCCTGTCCC[C/T]GAGATCCCTTTGACC	23077
rs568910187	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77138674	ATGAATTCTCTCAAA[A/G]ACTAGGATTTAACTT	23077
rs568926573	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77155760	TATTCAATCAATACA[C/T]ATTGAGGGGCTTCAC	23077
rs568942744	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77210366	CCCGGCTAATTTTTC[A/G]TATTTTTAGTAGAGA	23077
rs568952825	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77182694	TTGAGTGGTAAAACA[C/T]ACTACTCTGCTACAT	23077
rs568953254	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77150500	TCCATCTGTATCTCT[G/T]ATTCGATTAACTTGA	23077
rs568959078	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77109614	AATAGCAAGGCTGGA[C/G]TAGATAACCTCTTGT	23077
rs568976189	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77225684	GAAGAATCTGTAGCT[C/G]TTAGAAGTGATAGAT	23077
rs568976321	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77215996	AGTGTCTAATACTAT[A/T]CCCCACTAAAAAGAA	23077
rs568988386	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77177520	AGAGATAGGGTTTTG[C/T]CATATTGCCTAGGCT	23077
rs568990224	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77148487	TATATCTACTTTGAC[A/G]TCTAGTCCCTCTTAC	23077
rs569002410	snp	C/T	0.00119737	0.0244387	intron-variant, nc-transcript-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076923	AGAGGACTCATTAGC[C/T]GATTCCGCAGGTTTT	23077
rs569014183	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77131940	ATGCCAAATGCTCAT[A/G]CAAATAAAAGAAAAA	23077
rs569030420	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77256960	AGCACTATTCACAAT[A/G]GCCAAGATTTGGAAG	23077
rs569032473	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77170826	ATGATCTGCCTTCCT[C/T]GGCCTCCCAAAGTGC	23077
rs569034249	snp	A/G	8.57111e-05	0.00654585	intron-variant	MYCBP2	GRCh38.p7	13:77093149	CTATTCAACAGACAG[A/G]AGAGAACTAAAATAC	23077
rs569044112	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77099710	TCCCTTGGAAACCAC[A/T]GAAACGGTGGATCCT	23077
rs569062925	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77149054	CTCCTAATCAGCACT[C/G]AAATATGTAACTCTA	23077
rs569072636	snp	G/T	0.000399281	0.0141238	missense	MYCBP2	GRCh38.p7	13:77059624	TACTCGTGGTGGGTT[G/T]GCCTAGGTTCAAGCA	23077
rs569074047	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77108874	ACACCCAGCTAATTT[G/T]TTGTATTTTTAGTAG	23077
rs569089753	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77226571	CTAAACAAGTGTGTA[C/T]TATATGAAGATACAT	23077
rs569095628	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77100333	TCTGCCCCAGTCTTT[A/G]TCAAGGGCAGGTATT	23077
rs569112954	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77141758	CCTGTGCAACAGAGT[A/G]AGACTCTGTCTCAAA	23077
rs569125894	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77293804	CAGCCTCTACTATAG[A/C]AACTGGAAAGGCAAA	23077
rs569137962	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77301388	AGATCGCGCCACTGC[A/G]CTCCAGCCTGGGCTA	23077
rs569150070	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77197468	CATGAATTCAGTTGA[C/G]ATATTATGACTGATA	23077
rs569154664	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77242065	TCTTTAGTAATACAT[A/G]TATTTATCTTTGCGT	23077
rs569181897	snp	G/T	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77045847	CCCCTCAATTTAGTC[G/T]GGCAGAACATTATTT	23077
rs569187063	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77294784	TAATGAGAAGGGATA[C/G]AGTGAACAGATTATT	23077
rs569250587	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77142540	TAAAGCAGGGTTTCC[C/G]AAATATTTTGGTGAA	23077
rs569251039	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77178904	GCATCCTGCAGAGTA[C/T]ACTATCAAAGGAAGG	23077
rs569257776	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77186294	TAAAGTAGTTAAGCA[C/T]TTCTAAAAACAACAT	23077
rs569260942	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77235073	GTTTCTTTAAATATA[G/T]TTGAGTCACTAATTT	23077
rs569264365	snp	G/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77089479	AGTAAGATAACTTAA[G/T]CATCTGACTATAATT	23077
rs569266168	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77079876	CAACCTATAACATAG[A/T]GGAAGCCTGTTAAAA	23077
rs569267551	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77241200	GGCAAAAGAATATTC[C/T]GCAATCACCAAGTTA	23077
rs569271291	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77207972	GCCCCACCCGCCCCA[A/G]CCCCAGATGAATGAG	23077
rs569305176	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77249737	TGGAGAGATCCAGGA[C/G]AATAAATTTCAATTC	23077
rs569311364	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77141878	TGAATTATTATCTCT[G/T]CTTGTCTATGGTCAA	23077
rs569312396	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326392	ACACACACGCAAGCA[C/T]ACACACACGCGGGTG	23077
rs569323985	snp	C/G	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77088565	TTCTGAGTATAAAAA[C/G]CTTTTAAAAAAAAGA	23077
rs569347218	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77306112	ATTTGTAGATAATTA[C/T]ATTTATAGAAAATAC	23077
rs569403659	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77211663	TTATTTAGCAATAAA[A/C]AATGCATAAAACTCT	23077
rs569405223	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77080466	CAGTTAGTGCTATTT[C/G]TTTCTTGGTTGTTAA	23077
rs569407380	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77191571	AGTTATATTATGCTC[C/T]AGTCTTCCTAAGCTT	23077
rs569409153	in-del	-/TTGAA			intron-variant	MYCBP2	GRCh38.p7	13:77159905	TTTATTATATATCTG[-/TTGAA]TTTATTTTTATTTTG	23077
rs569427089	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77163797	TGCATATACAAGCAA[C/T]CAACAAGTCTTCAAG	23077
rs569431918	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77266197	CTTGATATTAGTACC[C/T]ATGTGTTATAGCGGA	23077
rs569441090	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77272776	TATACTCCTTTTGCT[A/G]TCTTTGGTCTGCTAA	23077
rs569444834	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77179812	AGCAATGTTACTCAT[A/C]TTCCAGCAGTGAGAA	23077
rs569462370	snp	G/T			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77080685	AGTGGCTCATGTCTG[G/T]AATCCTAGCACTTTG	23077
rs569479024	snp	A/C	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77233412	TTTCCCCACTCCAGC[A/C]CCCCACCCCCACCCA	23077
rs569481906	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77280194	TGGAAACAACAGATA[C/T]AGCTAAGAAGTCAAA	23077
rs569487744	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77170870	ATGAGCCACCATGTC[C/T]GGCCATAACCATGTT	23077
rs569496435	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77318170	TTTCCACTGTATAAG[A/G]ACTGGTTGGCCTGCT	23077
rs569517374	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77318741	CCTGGGTGACAGAGC[A/G]AGACTCTGCCTCAAA	23077
rs569525428	snp	A/T	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77235968	GGCTGTAGAGATAAA[A/T]GTATATCCTTCATCC	23077
rs569527863	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77137489	CAGGTGTGGTAGCTC[A/G]TGCCTGTAATATGAG	23077
rs569531066	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77108766	TAAAGTGCAGAGGCA[C/T]GATCTCAGCTCACTG	23077
rs569547149	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77230370	TCAGTAGATAAACTA[A/G]AAGATAAACTGGGTA	23077
rs569552291	in-del	-/T	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77222497	TCCCTTTTGTTGCCA[-/T]TTTTTTATGCAGTGC	23077
rs569555055	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77310757	CAGGATACACACACA[C/G]AGAGACACAGACGTG	23077
rs569560122	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77118125	ATGTGATGCTTACCA[C/T]AGTCATGCATATGAA	23077
rs569566858	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77096973	AACAATATCACTTCC[A/G]TAGGAAAAAGCCTAT	23077
rs569574701	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77189481	TAAAAACCAAACAAA[C/T]GAAAAAACCTTTTGG	23077
rs569575424	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77053569	ACTCCAGCTGTTTCA[A/C]TTTTCTATATCCTCT	23077
rs569582925	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77244690	TAAACTAAAGAGCTT[C/T]TGCACAGCAAAAGAA	23077
rs569590489	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77245229	AGAATCAGAAATACC[A/G]TTTGACCCAGCAGTC	23077
rs569602790	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77213465	CCTGGATGACAGAGT[A/G]AGGCTCTGTCTCAAA	23077
rs569604095	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77263262	ATTTCAACGAGAGAA[C/T]TATGTATATTGTTGT	23077
rs569637498	snp	A/G	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77175734	GGGAGGCCAAGCGGA[A/G]TGGATCACTTGAGGG	23077
rs569653882	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77145342	GACATTTTCCTGGCT[C/T]TTTTCTTATCTCACT	23077
rs569661618	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77298270	TCCTGCTAACCACTA[C/T]TTATCTTCGAGGTCT	23077
rs569671123	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77254552	GTGAGTTTTCATACA[C/T]GCATATAATGTCTAA	23077
rs569673062	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77262372	AATTTTTTAAATATA[C/T]GACAAAAAAATTTAA	23077
rs569694320	snp	C/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77130038	AAATTAACATCTTCA[C/T]AAAATGTTTTACTGA	23077
rs569708969	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77253320	AAAAGACATTTACTA[C/G]AATGTTCACAGCAAC	23077
rs569728547	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77182679	TCTTGCCCCTGGAAA[C/T]TGAGTGGTAAAACAT	23077
rs569758143	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77247411	GAGAACTACAAAACA[C/T]TGCTGAAAGAAATTA	23077
rs569760667	snp	A/C	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77261798	AGACTTGCTCAACTC[A/C]GGGTTGTCACAAACC	23077
rs569762388	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77275901	AGGCAGGAGAATAGC[C/T]TGAACCCAGGAGGTG	23077
rs569765214	snp	A/G	1.68658e-05	0.0029039	intron-variant	MYCBP2	GRCh38.p7	13:77190363	AACAATGATACCAAA[A/G]ACAACATGATCATTA	23077
rs569766008	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77283048	TATGCCTTACTAACC[A/G]GAGTACAAAGTTACT	23077
rs569802688	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77290208	AATGGCTAAAATAAA[C/T]AGTGACAACACCAAA	23077
rs569821096	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77166812	TTATAAAACAAAATC[C/T]AAATTTAAAAAGCAA	23077
rs569830074	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77321858	GGCCAATGGTTAGTG[C/T]CAAGTAATAATCCCT	23077
rs569836543	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77255300	CTGCAATCAGTATGC[A/G]CTGTATGTGTCTTAC	23077
rs569837593	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77174592	CTGAAATTCTTTGTC[A/G]TATTTACAGATGATA	23077
rs569844217	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77254615	GATAACTGGGATATT[C/T]TAAATTCTCTCTTCT	23077
rs569857533	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77072935	AGTCTCTTTTAGATA[C/G]TTCTTTCATCTTGTT	23077
rs569874858	snp	A/T	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77173954	CCACTATCTGAGTAC[A/T]GTCTATCTGATCATT	23077
rs569875035	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77283714	CCAGCCTGGGCAATC[C/T]GGCAAAACCCCATCT	23077
rs569904385	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77195505	GGGAAGCTGAGGCAG[A/C]AGAATTGCTTGAACC	23077
rs569904893	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77214451	GTATTACATGGAGGT[A/G]AAAAAAAAAATGAAG	23077
rs569919785	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77269499	AAAAATTAGCTAGGC[A/G]TGGTGGCATGGGCCT	23077
rs569924167	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77282022	CAGAGATAATATCTA[C/T]AAATAATAAAAAATT	23077
rs569956611	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77147005	AGAATGGACAGATTA[C/T]GGAATAGATCCCCAA	23077
rs569968174	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77056543	AAAATGCCAAGAACT[C/T]TCTCCTTGTTTTAAC	23077
rs569975519	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77321265	AAGATTTTTTTCTTC[A/T]CTTGAGTTAGGAAAC	23077
rs569999484	snp	A/G	3.30256e-05	0.00406346	synonymous-codon	MYCBP2	GRCh38.p7	13:77270010	AGCATACCCTAACCA[A/G]GACTTTTTTTCTTTT	23077
rs570002049	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77153487	ATTACAGACACTATT[C/T]TTATACATACTATTT	23077
rs570010324	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77285338	TTCTAACTAAAAAGT[A/C]AATTATACAAGTCCT	23077
rs570012324	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77175828	TGGGCATAGTGGCAC[A/G]TGGCTGTAATTCCAG	23077
rs570029200	snp	A/T	1.64955e-05	0.00287184	synonymous-codon	MYCBP2	GRCh38.p7	13:77098793	ATGGTTGGGGGATAA[A/T]GACCTACTGTGGGAA	23077
rs570036045	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77306795	GCAAATAACTAAGAA[C/T]ACAGAGATACAAGGC	23077
rs570048869	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77284554	CTGCTTGCCTCTGCA[C/T]AGAGGCATCTCATCA	23077
rs570060376	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77160574	AGTCACAAAACTTCT[C/T]TGAACTTCAGTTATT	23077
rs570075392	snp	C/T	1.66374e-05	0.00288417	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081412	AAGAGCCGTAAATCA[C/T]GTTTGCTTTCTTACC	23077
rs570104488	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77057295	AAATTGGGATACTAT[C/T]AACTAGGCCTTTGGC	23077
rs570120433	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77310585	ATATGATTATAGACA[C/T]ATATGATATCAAACA	23077
rs570126236	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77199712	GAAAGGGCAGACTGC[C/T]TCCTCAAGTGGGTCC	23077
rs570126914	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77299687	CTTACACATTAACAA[C/T]TTAACTTGGAATTTC	23077
rs570136050	snp	G/T	0.0023933	0.0345097	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77080667	TGAAGATAGGCTGGG[G/T]GCAGTGGCTCATGTC	23077
rs570142971	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77090816	AGTGTTGTATTTACA[C/T]TCTATAAAAGAACTT	23077
rs570170549	snp	A/G	0.000148541	0.00861674	missense	MYCBP2	GRCh38.p7	13:77097730	GCATGGACATTTCAA[A/G]AGTGGTCTCGGTTTT	23077
rs570176444	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77050930	TGAAACAGAGCTTTC[A/C]TATAATGTTTACATA	23077
rs570177636	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77222259	GGTATTATGTCATAT[C/T]CAGCAGACACATCTG	23077
rs570183598	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77300395	CATAAAGAGAGGAGT[A/G]TGCATATATTACAAT	23077
rs570186442	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77277517	TGAGTCCCCACATGC[A/G]ACCAAAAAAGAAAAA	23077
rs570206059	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77132333	TGTTATTAGGTAAAA[A/G]GGAATGAAATTGGAT	23077
rs570208733	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77073766	GGAAAGTGAAATAAA[A/C]AATACCATTTACAAT	23077
rs570215033	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77082710	TTTTGGTTTTTGTTT[C/T]TGAGATTTCATTTTC	23077
rs570238064	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77311558	AGGGAAAGAGAAGTT[C/T]TTTTTTGTTTTTTTT	23077
rs570238513	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77102240	GGTTACATGATACTA[C/T]ATGCTATTACACACA	23077
rs570252316	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291744	TGCACTCTAACCTGC[A/G]GAACAAGAGCGAAAC	23077
rs570275555	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77132412	GCTATACAAACAAGA[C/T]TAACAAATGATACTT	23077
rs570276319	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77091622	CCACTCAACTAGCCC[A/G]GTTGTGACAAAGTTA	23077
rs570279216	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77105433	AAGTCTAAAAAAGGT[A/T]AAGTGACTAAAGAAA	23077
rs570290561	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77222935	TTCTGGCATATACAC[C/T]GTGACTGCGAGGAAG	23077
rs570298610	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77308465	GTGATCTTGGTATTA[C/T]TTTAATCTCTCTGTG	23077
rs570315225	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77134911	ACACGAATTCTAAAA[C/T]ATGAGTAAACAAGAC	23077
rs570322489	in-del	-/A	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77242023	TTGTCTTAATCCTAC[-/A]AAAAAAAAATTTACT	23077
rs570326784	in-del	-/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77214717	TCTACTACATACTTA[-/G]GTGATATGGTGTAGC	23077
rs570343483	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77131607	ACATTCAGGAAAATG[A/T]TAATTTTTCCAAAGC	23077
rs570351880	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77083421	TGCAAATGAATAAAT[A/G]TATCAATTCTAGTGT	23077
rs570367612	snp	A/C/G	0.00478085	0.0486577	intron-variant	MYCBP2	GRCh38.p7	13:77322192	TAAAATGACTACTTA[A/C/G]CCTCTTACAACCAAA	23077
rs570386275	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77107491	TCCGTTATCCTAGCA[C/T]TTTGGTAGGCCAAGG	23077
rs570390127	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77246399	AAGAGGAGAGAACAA[G/T]AATTCATTCTTTGAG	23077
rs570391076	snp	C/T	0.000298899	0.0122213	intron-variant	MYCBP2	GRCh38.p7	13:77146152	TATACTTTGAGAAAA[C/T]GATCCTTACCTCTTA	23077
rs570417078	snp	A/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77232191	TATGAAATTTTTTTA[A/T]ATTAGACTATGACAA	23077
rs570434109	in-del	-/TATC			intron-variant	MYCBP2	GRCh38.p7	13:77239993	GAAGAAAATAAAAAA[-/TATC]TATAAACTCACCTGT	23077
rs570447639	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77106854	TTTGTCACCCAGGTA[A/G]TCAAGCATTACCTGA	23077
rs570451927	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77194742	AGTAAGTGAATACTG[C/T]AGAATTCTTAAAAAA	23077
rs570482748	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77122430	TCCTTGGCCGGTCGC[A/G]GTGGCTTACGCTTGT	23077
rs570497519	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77246218	GCAGTTTAAAAGACA[C/T]AGCTAGACACCCTGT	23077
rs570500767	in-del	-/A	0.00266307	0.0363929	intron-variant	MYCBP2	GRCh38.p7	13:77165425	TTGAGTTCAAACTCT[-/A]AAACAATTTTATAAA	23077
rs570505691	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77138423	ATAAGCTAACTTTAT[A/C]AACGGATTTTTAAGA	23077
rs570513686	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77147511	TGCTCATCTACTTCT[A/T]ACTCCTCCTGTACTT	23077
rs570517985	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77131376	TTTAAAAATATAGCT[C/T]GGCATGGTAGTACAT	23077
rs570520944	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77108268	ACTCATAGCATATTA[C/T]TGAATATATTCCAAA	23077
rs570529498	snp	A/C/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77231319	AACCTCTGCCTCCCA[A/C/G]GCTCAAGTGATTATT	23077
rs570529724	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77168724	ATTACAATAATTGTT[C/G]GTTACTCTAATAACA	23077
rs570553137	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77276769	ACTCCTGGGCTCGAG[C/T]GGTCCTCCCACCTTA	23077
rs570559788	snp	C/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77094476	TGTTTAAAATTCTTC[C/G]ACTGTTTCCTCTGCT	23077
rs570566748	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77096057	AATTAATAATAAAGA[A/G]TTACACAACAAATAT	23077
rs570569702	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77267454	TAAATTAAATAAGGA[A/G]GAAAACCCAACTGCA	23077
rs570578896	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77321410	CTACCTATGCACAAA[C/T]ACAGATGTACACATA	23077
rs570582264	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77322182	GAACTTTTGCTAAAA[C/T]GACTACTTAACCTCT	23077
rs570595923	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77057472	TCATGAGAACTGAAA[A/C]TATAAGCAATGGGCA	23077
rs570598530	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77116612	AAGTAATTTCCATTG[C/T]TGGACTATAGGCAAG	23077
rs570615433	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77139870	TAGTCATTTTTTAAT[A/G]ATAAAATAAATGAAA	23077
rs570616435	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77113637	GGACAAAATGTCTTG[C/T]AAGCAACATCAGCAT	23077
rs570627852	snp	A/C	1.65932e-05	0.00288034	intron-variant	MYCBP2	GRCh38.p7	13:77270073	ATGGCCCTGCAAAAA[A/C]AACAAAAGTTAGTAT	23077
rs570633960	snp	C/T	0.00597247	0.0543191	intron-variant	MYCBP2	GRCh38.p7	13:77152983	GGCAGGAGAATGGAG[C/T]GAACCCAGGAAGCGG	23077
rs570635358	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77248057	AATAACGAGTTAATG[C/G]GTGCAGCACACCAAC	23077
rs570638070	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77315101	ATTGACATGAATAAT[A/G]ACAGAAAATCTGAAT	23077
rs570643247	in-del	-/A	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77206589	AAATTTAAATACTCT[-/A]AAAAAAAAACCCTGG	23077
rs570659688	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77099488	ATTAGAGAACTGAAT[G/T]TATGCATAGACACAA	23077
rs570665262	snp	A/G	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77171940	GAGTCTTGCTCTGTC[A/G]CCCAGGCTGGAGTGC	23077
rs570681679	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77209163	AGAAATTGATCAAGG[A/C]GCTGGCAGGGCATTT	23077
rs570707644	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77114169	TTAAAATAGGTAACT[C/G]AATTACATTGCAAAA	23077
rs570717101	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77255990	GATATAAAAATTGAG[A/G]GCAAGAAGTAGACAT	23077
rs570764780	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77125088	ATATTAATGAAATTA[A/G]AAGCCTGTTTTATAA	23077
rs570776122	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77209660	AAGACCACTCACCCA[C/T]AGTCTCTTGTTATTT	23077
rs570803383	snp	C/T	0.00106151	0.0230136	intron-variant	MYCBP2	GRCh38.p7	13:77278934	AAAGGAAAAAATATA[C/T]ATACTTTATGACATG	23077
rs570804837	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77263549	AGACACAAAATAGCT[C/G]CTACAACATAAGCTG	23077
rs570824589	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77154851	GTGATGCTTTTTGCA[C/T]TGTATAGAATAATTC	23077
rs570825859	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77133501	ATCCTGAATGAGTCC[C/T]TATCCTTAAGTAGCT	23077
rs570828869	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77308381	TGCTATGTCAAGATA[C/G]GTTAAGAGTACAGAA	23077
rs570829012	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77303189	AATACAAAAATTAGC[C/T]GGGCGTGGTGGCACG	23077
rs570830856	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77299755	CTTAATGAAGAATGT[C/T]TGGAATTGGTCCTGT	23077
rs570838187	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77278382	AGAAATGTGTGTGCA[A/C]GAACTTCAACTCTTA	23077
rs570843664	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77092149	GTATTTATTATATTA[A/G]TTTATAATTATAGTT	23077
rs570851076	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77154353	ATGGAGGAGAAAGAA[A/G]AGGAAGAAAAGAAGG	23077
rs570866930	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77300769	AGTGATTAGATAGGA[A/G]GCAGGCCAATGCGCC	23077
rs570871883	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77258997	CGGTGGCTCACGCCT[A/G]TATTCCCAGCACTTG	23077
rs570872687	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77255365	GCAGGGTAGGTATGA[C/T]TCTTATTAAAAAAAT	23077
rs570882449	snp	A/G	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77200207	CTTAAAGGAGCTGAT[A/G]GAGATGAAAACCAAG	23077
rs570885418	snp	A/C	0.00145138	0.0268995	synonymous-codon	MYCBP2	GRCh38.p7	13:77161933	CTCCTCAAGAATTTC[A/C]AGGTCTTCTTCTAAT	23077
rs570898072	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77273762	GTCTCATTATAAACG[A/G]AATTTAAGGAATCTA	23077
rs570922963	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77102759	ACTTAAAAACTTTAA[A/G]TTCATTATCAGTGTT	23077
rs570936451	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77250095	GGGCGTAGTGGCGGG[C/T]GCCTGTAGTCCCAGC	23077
rs570959459	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77258643	TCACTAGTTTAGGTC[A/T]TTTTGTTAATTATAC	23077
rs570973212	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77091710	ACTGATTTAATGAAT[G/T]CATTTATTCATCAAC	23077
rs570980681	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77083535	GATATATACACATAC[A/G]TATATGTAGGTATGT	23077
rs570987102	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77084667	GAGTATTCATCACGC[C/T]CACCCCACCTCTGGT	23077
rs570989337	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77088736	TGCCTTTTAATTTCA[A/C]ACAATTTCTGTTGGT	23077
rs570990645	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77293445	TGGATTCACACAAGA[C/T]TGAGTTTTGTCAGAT	23077
rs570998994	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77140655	AAGAATACAATATGT[A/T]CCAAATAAAGAAGTA	23077
rs571013697	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77233468	AGTTAATATCTTAAA[C/T]ATAATTTATAAAGTA	23077
rs571014308	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77184228	TAAAATTTCCTTTAT[A/C]ACTTCTTCTTTGATC	23077
rs571014985	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77143312	GCTTTCAATGTGGAC[A/G]GGCGCTGTCCAATCA	23077
rs571022633	snp	G/T	1.64961e-05	0.00287189	synonymous-codon	MYCBP2	GRCh38.p7	13:77185959	CTCTAAATCTAGGAG[G/T]GTAGCTGTGAACTGG	23077
rs571033311	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77251456	GACAGCATGCTAATC[C/G]AAGCAATTATACAAA	23077
rs571033609	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77177674	TCTAGTAAACCCCTG[A/G]ACATACTATGACAAT	23077
rs571042316	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77285539	CACCTGTAATCCCAG[A/C]ACTTTGGGAGGCCAA	23077
rs571057988	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77234274	ACTCTAAATTTGACA[A/G]GTTACCATTAACTGA	23077
rs571087356	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77286135	TGACAATATGATTAA[G/T]GATGGTGGTGTACTT	23077
rs571090390	snp	G/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77136297	TCTCATTTGTTAAAG[G/T]GCCCTACCTATGATA	23077
rs571123957	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77224031	AAAAATTATTCAAAA[C/G]CTTCAATGACTGCAT	23077
rs571155870	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77068131	CTAACTACCATTCTG[C/T]AACTTCAAAATCTTT	23077
rs571170962	snp	A/C	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77202845	GACAAAATTCAACAA[A/C]CCTTCATGCTAAAAA	23077
rs571193680	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77210471	TGCTGGGATTACAGG[C/T]GTGAGCCACCGCACC	23077
rs571202620	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77282081	GGGGGAAGAGGCAGC[A/T]GCAGAAAGAGAGGAG	23077
rs571238194	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77212391	AGTGCATTATTTTTT[A/T]AAAAAAAGTTTGAAA	23077
rs571243763	snp	C/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77287099	TCACCGTGTTAGCCA[C/G]GATGGTCTCGATCTC	23077
rs571264785	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77267115	CTCAAGATTTTAATA[C/T]AAACAGCCTCAGAAA	23077
rs571265024	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77175094	CCATCACACTCAGTT[A/T]ATTTTTTAGGGTGTT	23077
rs571274098	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77136680	TTTCAAATATTCATT[A/G]CATTTCTCAACCCCC	23077
rs571303099	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77141473	GTAGGAAATAAATGA[C/T]GTAAAATGTACAAGG	23077
rs571306948	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77095267	ACAATAGCTAATAAA[A/G]TGTAGGTCAAATACC	23077
rs571315582	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77275107	GGCAACTATTCTACA[C/T]TAGGGTATTGGCAAA	23077
rs571316543	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77165603	AACAACAGGTCTATC[A/G]CAAATGAATTGTTAC	23077
rs571324702	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77270698	AAAAGTTCATCTATA[A/C]GAAGCAAATCTCAAG	23077
rs571343003	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77167994	ACATTAAATTTATAA[A/T]CATTTTATACATAGT	23077
rs571350670	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77236830	TTGGGCCCAGTTGTT[C/T]GAGGCCAGCCTGGGC	23077
rs571385507	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77047328	TTCTTAGATACCTCA[C/T]CTTTAAAATAGACAC	23077
rs571394455	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77196801	ACGTGGAGACACAGC[G/T]TAGGCTGTTGTACAT	23077
rs571403935	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77119400	ATGTGAAAATTTCAA[A/C]TGAAGTACCTACACG	23077
rs571410481	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77069672	CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT	23077
rs571450880	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77312637	TAAAATGAAATACTC[C/T]CAATAATCCCAAAAT	23077
rs571452026	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77172465	AACTTGGTATGATTT[A/G]TATTTTTATCAGATC	23077
rs571487184	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77180710	ACTTGAGGCCAGGAG[A/T]TTGAGACCAGCTTGG	23077
rs571509286	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77319776	TTATCAGTATTAGTG[C/T]TCCATCTAGCACCAG	23077
rs571521824	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77268012	AGCCATACAGCTCCA[C/T]ATTACAGGTTTTTGA	23077
rs571532465	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77159783	TTAAACCTCTTTTCT[G/T]TATAAATTACCCAGC	23077
rs571547486	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77046505	AAAAACATTTCTGAC[A/G]TAAGAGAAGGAAACC	23077
rs571549372	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77289121	ATGTCCAGGAAGTAT[C/T]TAAGATAAACAAAAT	23077
rs571557074	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77079562	ACTCAAATCAACAAA[C/T]GCTGTGTACAAGGCT	23077
rs571566128	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77049091	CAACCTACAACTTTC[A/G]TTCAATAATTGCCCT	23077
rs571568881	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228375	AGCTGGGTGTGGTGG[G/T]GAATACCTGCAGTCC	23077
rs571585915	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77064033	TCAAGGAAATCTCAA[A/G]TCTCTTCTGGAAGTA	23077
rs571598917	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77190432	TATGTCAATGAAAAT[A/G]ATTCACTCTTTTACA	23077
rs571603897	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77189258	AAATCCTACCTTCGC[A/C]AGACCGAGTAGTAGA	23077
rs571605255	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77206203	CAAAGTAATTAAATA[A/G]GTACTACATCTCAAA	23077
rs571616352	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77110185	GATGTGCAAGTAGGA[A/G]AGATATCACTAAATT	23077
rs571618830	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77159815	TCAGGTAGTTCTTTA[C/T]AGCAGTGTGAAAATG	23077
rs571620495	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77316188	GGGAATTTACAAAAC[A/T]ATTAAAGTTAATAAA	23077
rs571628423	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77049785	GGATTACAGGTACCC[A/G]CCACCATGCCTGGCT	23077
rs571629320	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77328595	TCAGTGTTGACCAGG[C/G]AGCCCCTAACCCTGG	23077
rs571634739	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77198664	TTTGTTGGCCCTTTT[A/G]GATACGAATAGGTGT	23077
rs571635739	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77260173	GAGTCTAGGGAAAAC[A/G]TCCACAGAAGTCACA	23077
rs571672287	in-del	-/A	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77178952	TAAATGTAAAAAGTT[-/A]AAAAAATTTCTGACA	23077
rs571682949	snp	G/T	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77235540	CAGATAATTAAAACC[G/T]TTTTATACCACAAAA	23077
rs571693090	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77213304	ACATGGTGAAACCTC[A/G]TCTCTACTAAAAATA	23077
rs571695720	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77313741	TGTTATCCAAAATAC[C/T]AAGAACTTTTTTCCC	23077
rs571697645	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77268573	TCACCTGGGATTAAG[A/G]GTTCGAGACAAGCCT	23077
rs571698348	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77072026	GGATACAGTGGCTCA[C/T]GCCTGTAATCCCAGC	23077
rs571743141	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77104790	AGTTTCCGAGGATAG[C/G]GACTAAAGCTGGAAT	23077
rs571743650	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77211563	ATTCACAGTATCATG[A/G]ACACAGTACAGATTG	23077
rs571747607	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77243050	TTTTTCTCTGTAGCT[A/G]CATCTTACCTCTTCC	23077
rs571758313	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77320441	GAAGGCCAACTCTTC[C/T]TTGCAGAAGAGTACC	23077
rs571758633	snp	A/G	0.000253428	0.0112539	intron-variant	MYCBP2	GRCh38.p7	13:77096282	TGTATCCATATCATT[A/G]AAAGTATAGCTCCAA	23077
rs571775428	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77152317	GGCAGTTTACAGGTA[C/T]ATGGTTAAAATTTCA	23077
rs571784764	in-del	-/TTAA	0.00755907	0.0610114	intron-variant	MYCBP2	GRCh38.p7	13:77232690	GTTGTTTATATAAAC[-/TTAA]TTAATAAACAGTGGA	23077
rs571791471	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77056245	TCATGTATCTATTAA[C/T]ATTTGTAGCACCATA	23077
rs571796334	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77111706	ACCTTAGCTTAAACC[C/T]TACTCAGCTTTTCTC	23077
rs571810237	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77214840	ACATAGAAAAGTTAT[A/G]GTCAAAGTACTTATT	23077
rs571819753	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77260340	AGAGAAAGCATGCCA[C/T]CAACATAAATTTTCT	23077
rs571831159	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77253380	ATCCAAATGCCCAAA[A/T]ACTAGAAACAATTTT	23077
rs571854477	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77298343	GTTTCCCTAATATAC[A/T]CTCTCATTCATCGTA	23077
rs571879558	in-del	-/T	0.0182019	0.0936463	intron-variant	MYCBP2	GRCh38.p7	13:77222710	AATCCACATATGATA[-/T]TTTTTCAAATTCCCT	23077
rs571891475	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77256855	TGAAACTAGAACTCA[A/G]TATGATCCAACAATC	23077
rs571910918	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77145413	ACTACCGTTTAATTT[A/C]AGGAATGCCCCAGGA	23077
rs571918945	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77242767	TTGCCATTTCTAATA[A/G]TTATTGATAGTAGGC	23077
rs571962206	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77230222	CCTGTTAACAATAAA[C/T]CCACAGTTCTTACTC	23077
rs571964337	in-del	-/TA	0.00107651	0.0231753	intron-variant	MYCBP2	GRCh38.p7	13:77181654	ATAAATAAAACCATT[-/TA]TAGAGTTTTAGTGCC	23077
rs571968211	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77157150	GGTTGCAGTGGCACA[A/G]TCACAGCAACCTCCG	23077
rs571998429	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77268061	TATTGATGTCTAAAA[A/G]ATATTAATGATTAAA	23077
rs571998470	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77048486	TAAGTAAACTGTATA[C/T]GGCCATCTTCCCTAC	23077
rs572002725	snp	A/G	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77158374	GGTGTATCTCCTTCC[A/G]TGCCAGTCCTCTATA	23077
rs572012117	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77289401	TTAACCCAGGGACAA[G/T]GCTGGCACAACACTG	23077
rs572016130	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087034	AGGGTCTATTTCTAC[C/T]GTCTATTGTTTTTGT	23077
rs572035199	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77275234	ATTTAAAAAACAATA[C/T]TCTTCATGTAATGAA	23077
rs572035464	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77267437	ATTAAATAAAATTAA[A/T]TTAAATTAAATAAGG	23077
rs572052000	snp	A/G	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77143434	ACATTTGAACTCCAG[A/G]GTCCCCAGCATTTAG	23077
rs572055905	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77240888	TTTTACCAAACATGA[A/G]GGAGGGTGATCTAAG	23077
rs572056520	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77281510	CCCAACACATGCTTT[C/T]GCACTTCTCTTCAGA	23077
rs572084845	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77280804	CTTTGGTCACAATGA[C/T]GATAGGGAACTCTTC	23077
rs572088296	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77188127	CAAAATGTAAATAGT[A/G]GGTATATATGGTGAT	23077
rs572157423	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77070439	TTTTTTTTAGTTCAT[C/T]AGCTATTGTTAGCCT	23077
rs572169166	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77289643	TGTGATCCAGGCAAA[C/T]TGGTCTACTCTCAGC	23077
rs572180297	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77179997	GAAAGGCAAAAAAGA[A/C]AAACAATGCATTGGG	23077
rs572182890	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77219325	CAGAAGGAGGTCTCT[G/T]TGGTGGAAGCAGGCA	23077
rs572195765	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77298424	TTAATGTATTGCTTC[C/G]TCGCCAAGCTAAAAG	23077
rs572202369	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326925	AAGACAGCGACCTCC[C/T]TCTCCTCCTCCTTCT	23077
rs572202960	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77220150	CATGTCCTAGCACCA[A/C]GACCAAGAGAGTGGG	23077
rs572208244	snp	A/G	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77297806	ATAATCACAAAATCT[A/G]GTCAATTATATCTCA	23077
rs572233197	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77063517	GAGCCAAGATCGTAC[C/T]ATTGCACTCCAGCCT	23077
rs572233686	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77303267	GAACCCGAGAGGTGG[C/T]GGTTGCAGTGTGCGT	23077
rs572240507	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228433	AATCACCTGAGCCCG[A/G]GAGGTCAAGGCTGCA	23077
rs572242360	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77259364	ACCCAACTGTCTCTC[G/T]GATCCTCAAAAAGGC	23077
rs572246367	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77166190	ACCTTATTTATTCCT[C/T]GAATGCAATCCAGAT	23077
rs572283479	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77312858	TTCTATACTAGTTGC[C/T]TAAGAGGAGAAACTT	23077
rs572287484	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77312235	TGATCTGCTAGAAAA[C/G]CTAAGGTCAACATTA	23077
rs572288585	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77327234	TGTGCGGAATCTGAA[A/G]TAGTCCACTTCTCCG	23077
rs572292810	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77071360	AAATTGTAATATTTT[A/G]CCTACTTTACAGGTA	23077
rs572304118	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77055042	TGGTAGGTGAAGGTA[C/T]AGATGTAAAAGAGGT	23077
rs572307547	in-del	-/AATACAG	0.00438332	0.0466095	intron-variant	MYCBP2	GRCh38.p7	13:77088607	TTCAAATAGTAAAGC[-/AATACAG]AAATAAATTTCTTTA	23077
rs572330951	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77290522	CCATACCATGAAATG[C/T]TTACTCATCAAGGAA	23077
rs572334716	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77111301	GAGCTAAGTCATCCA[A/G]CCGAACTCATTTTTC	23077
rs572342477	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77213389	CTGAGGCATAAGAAT[A/T]GCTTGAATCTGGGAG	23077
rs572344448	snp	C/T	3.32524e-05	0.00407739	synonymous-codon	MYCBP2	GRCh38.p7	13:77205504	CACACTATAATCTTC[C/T]TTAGAATAAACCTTC	23077
rs572373642	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77252700	AAATAAACTCATAGC[A/G]TATATAGCCTTTTGG	23077
rs572384387	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77055844	AGCATGCACCTAAGT[A/G]CCAAGCATTGTGCTA	23077
rs572396787	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77216916	GTCAAAGGATTTGAG[-/A]AAAAAAAAATATTTT	23077
rs572400110	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77174183	TATATGAATTTGTAC[A/T]AGTATGTGCTAAGAA	23077
rs572409837	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77260263	GTGCTCCTAGTGACA[A/G]GATATGACAGAAAAT	23077
rs572441955	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77189866	TATGAGACTACAATA[C/T]ATCAACCAGGCCTGC	23077
rs572456070	snp	A/C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77206420	CATTATTTTTAAGGG[A/C/T]CTACCTCTGTGAAAA	23077
rs572509960	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77144886	ATGGTAGAATGGAGG[A/T]AGTGTCCTGGATCTG	23077
rs572512041	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77145617	TTTTTCTAAATTCTA[C/T]GGAGGTGATCTCTCC	23077
rs572531832	in-del	-/AAG			intron-variant	MYCBP2	GRCh38.p7	13:77246481	AGAAAGAAGAGAAGA[-/AAG]AAGAAGAAGGAAGAA	23077
rs572534215	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77138575	GTTAATATATAAAAC[A/G]AAGTGTGGGTTATTA	23077
rs572547618	snp	C/G	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77198034	AAAAAATCTCTTAGA[C/G]CTAGAAAAAAAAATA	23077
rs572547788	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77248332	GTAAAAACACAACCC[A/G]CAGACAGAACTTTTT	23077
rs572550235	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77244884	TCTTACAAGAAGACA[C/T]TTATTTATGCAGCAG	23077
rs572553575	snp	A/T	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77072342	TGGGAATAAGAAAAC[A/T]AAGAAAACATTGTGA	23077
rs572557870	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77194452	TGGTCTACATTAATC[G/T]CTGTTTTCCTAATTT	23077
rs572568895	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77275603	TGGAGGCAGGAGGAT[C/T]ACTTGAGTCCAGGGT	23077
rs572575175	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77282595	TGATCCCACCCCCTC[C/T]GATCTCTCACAGAAA	23077
rs572579359	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77278074	TTAATGAAAGTTGCT[A/G]AGTCAGAAGTTTAAT	23077
rs572586550	in-del	-/CACACA			intron-variant	MYCBP2	GRCh38.p7	13:77245778	ACACACACACACACA[-/CACACA]AAGGAAATAAAAACA	23077
rs572595098	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77145484	CTAGGTGACAACCAT[A/T]CCTCAGTTTTAAATG	23077
rs572602102	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77284033	AGGGAATAGAAAGCT[C/T]GTTTAAATACATCAA	23077
rs572619301	snp	C/G	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77215870	ATAGGTATGAGCCAC[C/G]ACACCTGGCCTATGA	23077
rs572650781	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77301057	AAAGCTCTAGATACA[C/T]AGACAGCTTTCCCAG	23077
rs572663367	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77129628	AAATGGAAATGATAT[C/T]GATTGTATAGAAAAT	23077
rs572665959	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77257349	TGGCTACAGTTGGCG[A/G]TAATTTTTTGTATAC	23077
rs572677777	in-del	-/TAT	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77325325	TTGACAGTTTCCTAC[-/TAT]GTTTTCCCCATGTAC	23077
rs572696680	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77276042	ATACGATTTATCCAC[A/G]TTTGTAATTATACAC	23077
rs572713921	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77248319	CAACATCAACAGAGT[A/G]AAAACACAACCCACA	23077
rs572719584	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77185525	GAGATTAAGTGTAGT[C/T]CCAATTTTTAATCTA	23077
rs572720876	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77230545	ACATTATGAGATATC[C/T]TGGGGATGGGACCCA	23077
rs572726935	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77210185	TTTGTATATAAAGCA[C/T]CACAATAATTTTTTT	23077
rs572738332	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77121711	ATACACAGTGAAATT[C/T]AGAAATGAGATAGGC	23077
rs572773631	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77315686	GATCACCTGAGGTCA[C/G]CAGTTCAAGACCAGA	23077
rs572776285	snp	A/G	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77199937	TAAAACCACAAAGAT[A/G]GGGAAAAAACAGAGC	23077
rs572785596	snp	C/T	1.68823e-05	0.00290532	intron-variant	MYCBP2	GRCh38.p7	13:77068514	CATTGCAACTTTTAA[C/T]AATGTTTCAAGTAAC	23077
rs572795411	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77092699	CCAAAGTGCTGGGAT[C/T]ACAGGTGTGAGCCAC	23077
rs572797313	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77125284	CAATAGGCATTAAAC[G/T]TCTGTATTTGAAAGC	23077
rs572798236	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77255697	ATATATTCTAGTAAC[C/T]TGCTCATTTTTAAAG	23077
rs572823095	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77092614	TATTTTTAGTAAAGA[C/T]AGGGTTTCACCATGT	23077
rs572826991	snp	C/T	9.89479e-05	0.00703307	synonymous-codon	MYCBP2	GRCh38.p7	13:77059613	TGCTTCTGAGCTACT[C/T]GTGGTGGGTTTGCCT	23077
rs572830365	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77186427	ACAATGCATGTTTAC[G/T]TGAAAGAAAAATAAA	23077
rs572830778	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77059046	TCACCACTCTCCGCA[C/T]CACCAAAATGCAGAT	23077
rs572854988	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77325733	CGAACAGAGGATGAA[C/G]AGAAATGGCCGATGG	23077
rs572862381	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77148218	GACAAATATTTATTT[C/T]GGATATAGAATTCAT	23077
rs572870915	snp	C/T	5.34374e-05	0.00516874	intron-variant	MYCBP2	GRCh38.p7	13:77099127	TTATATTGTTTGTCA[C/T]ACATACTAAAATACT	23077
rs572874060	snp	C/T	0.0103295	0.0711199	intron-variant	MYCBP2	GRCh38.p7	13:77050112	GCTGTAGTTAATAAC[C/T]TTGTTTATTTGCCCT	23077
rs572888955	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77233872	ACACAGAGAGAGAGA[C/G]AGAACGAGAGAGAGA	23077
rs572890835	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77260923	ATACCATTCTACTAA[A/C]ACATATCTAAAATCT	23077
rs572894583	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77200361	AGAATAAAAAGAAAC[A/G]AACAAAGCCTCCAAG	23077
rs572899796	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77217723	TGAAATATGCATATG[C/T]AACAATTATAATATA	23077
rs572903161	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77320711	CATATTAAATAGTGA[C/G]ACAACCTCACAACCT	23077
rs572905915	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77179097	CGAATTTCTTACGTA[C/T]GAATTTCATACAATG	23077
rs572929995	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77290162	ACTAGGAAAATGCAA[A/G]TTAAAATGAGATATA	23077
rs572943116	snp	C/G			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087055	TTGTTTTTGTTAGTT[C/G]TTGCTCATGGTGTCT	23077
rs572955086	snp	A/G			missense, utr-variant-5-prime	MYCBP2	GRCh38.p7	13:77225480	CTGCCCGGAGCTCAC[A/G]GTCAAATCGCACAGA	23077
rs572969857	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77285874	GAAAGGAAAGGAAAG[C/G]AAAGGAAAGGAAAGG	23077
rs572976685	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77142023	TTCCAAAAAACAAAT[A/G]TAAGTGGATTTTTCT	23077
rs572985189	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77083658	AAAGCTCCTTTCTAC[A/G]CAAATGGACCACAGC	23077
rs573006326	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77279337	CACAAAACAATTTAA[A/G]ACTGCTTAGCTAAAA	23077
rs573006738	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77099841	AGGCAAAGCATTAGA[A/T]GTTTCTGCATGGACA	23077
rs573011497	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77210481	ACAGGCGTGAGCCAC[C/T]GCACCCGGCCCAGCA	23077
rs573013136	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77218399	TTTTATCACTAAGCT[A/G]TAAGTTTAGATCTTA	23077
rs573023373	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77114775	AAAACATTATAAAAT[-/A]AAAAAAGTATTAAAA	23077
rs573025100	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77241256	ATGTTCCTTTATTTC[C/T]TATATGCACAAATAT	23077
rs573036406	in-del	-/G			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075674	TGTTGATTTCTTTTT[-/G]GGGGGGGGTGAGGGG	23077
rs573040642	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77149197	CTTAATTATGTGTTG[C/T]TTCTTTGGCTAGTAT	23077
rs573045318	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77178228	AGTACAAGCTTGTCT[C/T]ATCAGTCATAATGTA	23077
rs573107338	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77101959	TTTCACATTCATCTC[C/T]TAATTTATTTAATGA	23077
rs573108303	snp	C/T	0.000565596	0.0168071	intron-variant	MYCBP2	GRCh38.p7	13:77095319	AACAATCGCTGTTAA[C/T]CCAAAGGTGATTAAA	23077
rs573114738	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77060593	AAAAGCAGCAAAATG[A/C]AAACTATGTTTTAGA	23077
rs573115898	snp	A/T	0.00478085	0.0486577	intron-variant	MYCBP2	GRCh38.p7	13:77249356	AATATTCTGATATAT[A/T]CAGTTTGCTTCATTC	23077
rs573133532	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77268032	CAGGTTTTTGAGGTA[A/C]AATAATACATCAATA	23077
rs573150410	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77170937	ACTAAACAACTAGAT[A/G]GAGAATGGGGGAAAG	23077
rs573171737	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77094710	GCCTGACAGATTTCT[A/G]TTTATCCTTTGAGAC	23077
rs573191563	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77142301	ACAGGAATTGTCTTA[C/T]CCAGGAAAATGTATG	23077
rs573191696	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77106661	GGAGGTAGTGGAGCC[A/G]TCAGAAATTTTATAG	23077
rs573196327	snp	A/G	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77146046	CTCTATCGGCAACCT[A/G]GAAAAATGCTATAAA	23077
rs573233160	snp	C/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77103039	TCTATATTATAATAC[C/T]GAATAGGAGCATCAT	23077
rs573233561	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77310434	GTTATATTGGAACAC[A/G]GCCATGCTTATCCAT	23077
rs573234177	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77048032	TCTTGGAGGTAGGAC[A/G]AAGAACTCCTGGCAT	23077
rs573234484	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77163303	TAGCAATTTTCCTCA[C/T]GTGGCTAGAATACAA	23077
rs573243295	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77094300	TTTTGGAGTGTCAGT[A/G]CATGATGTGTGAAAG	23077
rs573256674	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77109876	TTGTGAAGATTTCAT[A/G]GACATTTATCAGTTC	23077
rs573267805	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77149310	TTTGAATTTGAATCA[C/T]TGCATATTTGTTTCA	23077
rs573283244	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77163929	TCATCTGCAGCCTCC[C/T]CTTCCTGTTCTGTGC	23077
rs573313615	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77264641	ATCTTGGCTAGAATA[A/C]CATATTTCATCAATA	23077
rs573316935	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77148745	CTTTTCTGATCGGTG[C/T]TTTCTTTTAATCTCT	23077
rs573318170	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77117597	TGAATCCGAAAAATG[A/G]TATACAAGCTGAAAC	23077
rs573329860	snp	G/T	0.00358779	0.0422022	intron-variant	MYCBP2	GRCh38.p7	13:77148382	CCACTCACACCAAAA[G/T]TCACAGACCTGTGAC	23077
rs573331693	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77155884	AAAAACAGGTGTAAC[C/T]TGGACACTTGGGGAC	23077
rs573341066	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77202287	AATAAACTAGAAAAT[A/C]TAGAAGAAATGGATA	23077
rs573343083	in-del	-/AGTGGTTTC	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77268312	GAAAATGAATAGCAT[-/AGTGGTTTC]AGAAGGTGTGGTATG	23077
rs573346563	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77310778	CACAGACGTGTGTGC[A/G]TGCGCATGCACACAC	23077
rs573347277	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77047392	TAAGTATCCTGGCAC[A/G]AGAAGGTAGTCAATA	23077
rs573348663	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77258741	ACAGTAGTTATTTAT[G/T]ATTATTATTAACAGT	23077
rs573363182	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77258005	TTGTAACTTTGTAAC[A/G]TAGCTTCAGTGAATC	23077
rs573363753	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77063237	TTGTCAGAAATACAT[A/G]CATGTCTAAAAGCTT	23077
rs573368254	snp	C/T	2.04581e-05	0.00319822	intron-variant	MYCBP2	GRCh38.p7	13:77156252	AAACACTGATCAGCA[C/T]CTTCAACAATTAATA	23077
rs573392419	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77294931	CTAACCAAAGTATCC[C/T]GTATCTCCGTGGTCA	23077
rs573401072	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77272840	AGGGTTGCCCAAGGG[G/T]CCAGAGAAGAGTAGA	23077
rs573404777	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77294414	TAAATGAATGAACTT[A/G]CTTACATCACTGTTA	23077
rs573436683	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77196877	CAGAGATAAATGTCC[A/C]TGAGGCTGGACCACT	23077
rs573437065	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77086348	CTCTTTTGAAAGCTA[A/G]TATTTTTTTCTGTGG	23077
rs573438252	snp	A/T	0.00597247	0.0543191	intron-variant	MYCBP2	GRCh38.p7	13:77302765	AAGTTGGAGTGGCTA[A/T]TTTAATATTTGACAA	23077
rs573448448	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77157636	ATATCTGTAATCCCA[A/G]CTACCTGGGAGGCTG	23077
rs573455386	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77175822	ATTAGCTGGGCATAG[A/T]GGCACGTGGCTGTAA	23077
rs573468539	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77323454	CAGAACATTCTTCCT[C/T]TACATCTGCCTCCTC	23077
rs573516252	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77173420	AAAGCTTTTCTTGAC[C/T]GGGGCAAAAGACTAG	23077
rs573520491	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77203146	TATATCTAGAAAACC[A/C]CATCATCTCAGCCCA	23077
rs573523460	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77301773	AAACCCAGATATTAA[C/T]GTTAGGAGGCAAGTA	23077
rs573557625	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77282214	TCAGGAGTTGCAAAC[A/C]AGCCTAGCCAACATG	23077
rs573564695	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77295586	ACTTAAAAGTGTAGG[A/C]AACAATTGCCTCTAT	23077
rs573578871	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77295175	GAGTCTTACTCTGTC[A/G]CCAGGCTGGAGTGCA	23077
rs573584489	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77100742	CTTTTTAGTTTCTTG[A/C]AAAGCTTCATTATTC	23077
rs573590557	snp	C/T	0.000335976	0.0129567	intron-variant	MYCBP2	GRCh38.p7	13:77150989	AATACCATTATTATT[C/T]AATTGTCACTGACAT	23077
rs573607221	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77046718	ATCTCAGAGAAGTCA[A/G]CTTCAGGTTAGAGCT	23077
rs573619007	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77052610	CAGAATATTAAGTAG[G/T]AAAAGCTATGCTTTT	23077
rs573627735	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77303320	CCTGGGCGACAGAGC[A/G]AGACTCCGTCTCAAA	23077
rs573636569	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77099175	AAGGGGGAAATATTT[C/G]TAATAAAATTTCTAC	23077
rs573659753	snp	A/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77249937	ATTTGTTTTTAAAAG[A/T]TCATGGCCGGGCGCG	23077
rs573663103	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77166816	AAAACAAAATCCAAA[C/T]TTAAAAAGCAATTCC	23077
rs573663326	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77053882	TTTGTATCTAGTAAG[C/T]GCAAAGTACTAGAGA	23077
rs573674204	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77317232	GCTGGGATTACAGGC[A/G]TGAGCCATCGTGCCC	23077
rs573682210	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77302324	AGAAGAGATATGCTT[A/G]AAGGAACAATAAAAT	23077
rs573685572	snp	A/G	0.00676609	0.0577691	intron-variant	MYCBP2	GRCh38.p7	13:77289475	TCAAATAAACACAGA[A/G]AGATCACTTGACAAA	23077
rs573694167	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77210971	TAAACCTAGGTAGTG[G/T]TGCTTAAAATGCATG	23077
rs573699512	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77195313	ATAAAAAGTCTGAAA[C/T]AGGCCAGGCCTGGTG	23077
rs573706177	snp	A/G/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77171716	CATATCTAGATCTGA[A/G/T]ATCCTCATTTAATTT	23077
rs573714476	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77317755	CATCCTGGTCCACAT[A/G]GTGAAACCCCGTCTC	23077
rs573724745	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77061527	TTTATAGATGGTAAG[C/T]GAGACAGCTGTGAAC	23077
rs573760866	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77085320	GGAAGAAAACCAATT[A/G]TTTCAAGTTTGTTAA	23077
rs573766706	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076608	ATTTCTTTTAGATAG[C/T]TCCTTCATCTTTCTA	23077
rs573767137	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77203451	GGAAGAATCAATATC[C/G]TGAAAATGGCCATAC	23077
rs573777402	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77311841	AGAAGAAAGACACAA[A/T]GGTAGAAAACATTCT	23077
rs573797946	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77054488	AGGCTACTGTAATTA[C/T]CAAGGAAAATGATTA	23077
rs573800827	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77187585	ATAATGGTACGCAAA[C/T]GGAGAAGACTGACAG	23077
rs573801428	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77134293	CCAGCACTGTGGGAA[A/G]CCAAGGTAGGTGGAT	23077
rs573821463	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77242457	TTTTAAGCTCATAAA[C/T]AATGAGGAAAAGATA	23077
rs573840469	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77311017	AAAAGCAAATTCTGG[A/G]GGGGAGTCAAAACTT	23077
rs573853776	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77272938	TTGCCTATAAGGATT[A/G]TTTTTCCCACCACTA	23077
rs573865970	snp	G/T	0.000399281	0.0141238	missense	MYCBP2	GRCh38.p7	13:77125423	CACAGAACTCTACCA[G/T]GCTGTTCTGATCCAG	23077
rs573877665	snp	C/T	0.00140108	0.0264306	missense	MYCBP2	GRCh38.p7	13:77205339	CGGCACTGAAACGTA[C/T]AGCTTCTACTGAATG	23077
rs573880344	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77325814	GCCCGGTTATCAAAG[C/T]ACAGCTCTAAAAATC	23077
rs573880586	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77186782	ATCCCAGAGCTCCTG[A/T]AAACGAGTTTATAGA	23077
rs573904261	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77169125	CAAATGTAAAGCCAA[C/T]AGGCCGGGCGCGGTG	23077
rs573907971	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77157201	CTCCCACCTCAGCCT[C/T]CAAGAAGCTGGGACT	23077
rs573908758	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77254836	ATTTTTTAGTTCCCA[C/T]ATATGAGTGATATTT	23077
rs573925910	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77234613	TGTTAACAGAAGAAT[A/C]AGTTCTCAATAATGC	23077
rs573966518	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77164040	ATACAGTCCCATGTC[C/T]TTAAATAACGATCAT	23077
rs573990928	snp	C/T	0.000103609	0.00719679	missense, utr-variant-5-prime	MYCBP2	GRCh38.p7	13:77273636	TCCCAGTACTTCGAA[C/T]GGTGATTTCCAAAAG	23077
rs573993024	snp	C/T	0.000264539	0.0114978	synonymous-codon, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326623	GGGTAGCCCCAGCCC[C/T]AGCCCCGCAGCAGCC	23077
rs574004258	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77226011	TAGATTTCCTAAATA[A/G]ATCTTAGAAAGGCTA	23077
rs574043166	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77197466	AGCATGAATTCAGTT[A/G]AGATATTATGACTGA	23077
rs574055360	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77066376	TTTCTAGGGCACATG[A/C]GGATAATGTGGAGCT	23077
rs574056840	snp	G/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77266562	TTATATATGGGAAGT[G/T]GGATTATAATTATTT	23077
rs574063014	in-del	-/TGTGTTG	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228691	CTAAGATGAATATGT[-/TGTGTTG]TGTGTGTGTGTGTGT	23077
rs574072800	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77157710	AGCTGAGATCATGCC[A/G]CTGCACTCCAGCCTG	23077
rs574088794	snp	C/T	1.64827e-05	0.00287073	missense	MYCBP2	GRCh38.p7	13:77212093	TATTTTGATCCAATG[C/T]TAGGCATGGGAGCTG	23077
rs574095476	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77265766	AAGAAACAAGAAAAT[A/T]ACAAAAGGCTTCTTC	23077
rs574100323	snp	A/G	0.00597247	0.0543191	intron-variant	MYCBP2	GRCh38.p7	13:77174896	GCTAGAATATTAGCC[A/G]TACTATATATATATA	23077
rs574112789	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77320793	AAAAAATTTTCTAAT[C/G]AACACCTAATAAACC	23077
rs574113814	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77226969	AATAGAGTGTGGTTA[A/C]CTACATTATATTTCA	23077
rs574114911	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77195574	TGCACTCCAGTGTGG[G/T]CTACCAAAGAGACTC	23077
rs574118376	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77295670	ATTCAGGAATCATAG[C/T]TACGACTCCTCTCTT	23077
rs574120941	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77065664	AGAAACTTCCACTTT[C/T]GAGAGCTCTCTTCCT	23077
rs574124491	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77194011	GCAATACTTATATTG[C/T]TTAATATATAATTTA	23077
rs574170110	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77208403	GTGTAAAACTCTGTG[C/T]GTAGATACCTGTGTA	23077
rs574192934	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77057663	TGGCTTCTGAATATT[G/T]TATACATTCTGTTGA	23077
rs574231574	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77078250	TTGAAAACAAGCAAG[C/G]AAGCAAGCGATTGGC	23077
rs574237005	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77188850	AATCTGAGTTTATAA[A/T]TCTAGGCTAAGATAA	23077
rs574250279	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77143565	TCTCAGGATCTCCAG[C/T]TTGCAGGTGTGGCCC	23077
rs574254019	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77135992	AGGCGTCCACCACCA[C/T]GCCTGGCTAATTTTT	23077
rs574257190	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77240511	TACTCAAGAGGCTGA[C/T]GTAGGAGAATCGCTT	23077
rs574271906	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77208144	TCATTTTTTCTTTTC[C/G]TTTTCTCCTCCTGCT	23077
rs574278305	snp	C/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77296536	TATTTTTTAATCTTG[C/G]CATTTTTATTCAAAT	23077
rs574279639	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77209261	CTTGAGAGTTCTGTT[A/G]AGACCCCACGGAAAT	23077
rs574289535	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77095291	AAATACCGAACTACC[C/T]TAGATATCAATAAAC	23077
rs574297325	snp	A/G	0.000399281	0.0141238	missense	MYCBP2	GRCh38.p7	13:77098359	GTGCAGACTTCGACC[A/G]CCTCACTGTGGAGGT	23077
rs574302115	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77188189	TTTTAGGATACTTTT[A/G]TCTCATTCCTACCAG	23077
rs574303984	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77313962	AACGAGATTCTACTA[C/T]ACACCTATCAGAATG	23077
rs574308343	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77168026	TTTTTAACATTATGT[A/T]TAGACTACTTTAAAT	23077
rs574311941	in-del	-/AT	0.00557542	0.0525036	intron-variant	MYCBP2	GRCh38.p7	13:77051310	AAACTGATGATACAC[-/AT]GTTTGAAAACTAACA	23077
rs574313320	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77151042	TAAACTCATAATTAT[G/T]TATACTTTATGTTAG	23077
rs574325301	snp	C/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77182063	TAAATTGTCTTGTTA[C/T]AGAATAATACTACAT	23077
rs574329751	snp	G/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77259173	GGGAGGCTGAGGTGG[G/T]ACAATCGCTGGAACC	23077
rs574333168	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77160123	CTGGGCTGGAGTACA[A/G]TGGCATGATCTTGGC	23077
rs574349258	in-del	-/T	0.00199481	0.0315187	utr-variant-3-prime	MYCBP2	GRCh38.p7	13:77045025	CAATGATTATTTTTC[-/T]TTTTTTGCTTGAAAG	23077
rs574363153	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77328101	TAAGTTCTGTCATCC[C/T]AGTACTGTATCTTTC	23077
rs574371216	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77113181	CCTTCCTCATCTCCA[A/C]TCCTCCTTGCCTGAT	23077
rs574371964	snp	C/G	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77091818	CCTCAAAATCCTAGG[C/G]TGAAGCCATCCTCTT	23077
rs574383986	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77231492	CCTCAAGTGATCCAC[C/T]CCCTCAGCCTTCCAA	23077
rs574390162	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77144125	ATGCTTTCTGCTCAC[A/G]GTCAGGAGAGGCACA	23077
rs574415170	snp	G/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77106947	AGCTTGAGGAGGTTT[G/T]ATAAATAAGTCTTGT	23077
rs574432870	snp	A/G	0.000399281	0.0141238	missense	MYCBP2	GRCh38.p7	13:77098948	ATCTGCTGTGTTTAG[A/G]GGACAGCTCTGATTT	23077
rs574436559	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77152423	GTCAGGGATATACTG[G/T]ATAGGAGAAGGTGGT	23077
rs574436852	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77179882	CAATGGGGCAGATGA[C/T]GACCTGCTCTATGAG	23077
rs574443205	snp	G/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77160855	ACCTTTCCATCTGGG[G/T]CTATTAAAATGTCTT	23077
rs574447527	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77240280	AAAATGAATACATAG[A/T]TAGAATTCTTGTCCA	23077
rs574449891	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77232946	ATTGTAAAATATCTC[C/T]TTTATGAAAGCTAAC	23077
rs574475302	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77050225	TATTAAGCTGTTTTC[C/T]GGAGAGGTCTATCAC	23077
rs574475824	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77209231	AAGACAAGGTTCAAC[C/G]AGCTGAACATCATAC	23077
rs574499603	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77269007	CTGTTCAGGTAGGTA[C/T]TGTATGGAAAAAAAT	23077
rs574501698	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77176748	ATAAAATTAGCCATT[A/C]GTATTTTCCCATACA	23077
rs574506376	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77116869	AATTATGCTTGTTTT[C/T]GTAAAGACTTGCAAT	23077
rs574512627	snp	A/C	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77307644	AAAAAAAAAAAAAAA[A/C]AAAAAAAAAACTTCA	23077
rs574512757	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77255450	TAGGTGTAAATGTAC[A/G]CTCAATTTTCACAAG	23077
rs574553869	snp	C/T	0.00478085	0.0486577	intron-variant	MYCBP2	GRCh38.p7	13:77114993	ATCAGTATAAACCCA[C/T]AATTATCATACATCA	23077
rs574557091	snp	A/C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77199374	GATTATATCCTGCAC[A/C/G]TGACTCGGAGGGTCC	23077
rs574575242	snp	C/T			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77085712	TTTCTTGAATGCTTC[C/T]GGCATCTGAACAAAC	23077
rs574576817	snp	C/G	5.73126e-05	0.00535285	intron-variant	MYCBP2	GRCh38.p7	13:77262016	TAATCTCTTAAATCA[C/G]AGAATGCTCATTTTT	23077
rs574582268	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77050743	CAGCCATCTTTTCAC[C/T]AATCCTTAGTAGACT	23077
rs574602408	snp	A/G	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77193582	ATTGAGATAATTCTT[A/G]GGATTACGTAGAGAG	23077
rs574615275	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77123763	TAAGCTAGAAAAGTC[A/C]TTTAGAAGTCACCTA	23077
rs574617384	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77281007	TAGCTATGGATTATT[A/G]CACAGAGGTAACAGA	23077
rs574648815	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77299342	GGCATTTAATTGGTT[G/T]TAACAATTCTTATGA	23077
rs574656857	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77154454	TATGGTTAAAAAAAG[A/G]ACTCTAAGATGAAAA	23077
rs574686505	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77139535	ATATGGTAATTCATG[C/T]GGCAAGACTGTAAAA	23077
rs574689325	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77262798	TATGACTTTGTCCAG[A/C]TATACAAACTACTAA	23077
rs574690869	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77115793	TTTTCTAGTTAACCA[C/G]GATCTTGAGTTATGA	23077
rs574694159	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075154	TTGAGGTTGCAGTGA[A/G]CCGTGATCATACCAC	23077
rs574701362	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77271214	TACCATATTTGTTTC[C/T]GCTAATTCTCAATAA	23077
rs574710422	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77050716	AACTTCATATGACTT[C/T]TTAGTGCTGAACAGC	23077
rs574776843	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77264355	GCAATGGAGGCAACA[A/C]TCTACTCTCAGACAT	23077
rs574780281	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77090633	AAGAAAATGGATATG[C/T]ACACATGAAAACCTA	23077
rs574783184	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77155236	TTGGCATTGTACTTC[C/T]TCACGCTATAAATGA	23077
rs574787704	snp	C/G	1.65583e-05	0.00287731	missense	MYCBP2	GRCh38.p7	13:77140062	CTCATCAATAAAAGT[C/G]ATAGTTCCATTGACT	23077
rs574817467	snp	A/C/G	3.29567e-05	0.00405924	synonymous-codon	MYCBP2	GRCh38.p7	13:77180211	GAGGTGGGAGGAGAA[A/C/G]AGTTCATTTTCTCTC	23077
rs574823493	snp	C/T			intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77073601	TAGAAAGGAAAAAAC[C/T]CAAATTTATTGAAGA	23077
rs574836935	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77278422	TTCAGTGGAACACAG[A/G]AAAAAATACTCTAGA	23077
rs574853759	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77314838	GGGATGTTGATATGG[A/G]TGAGGCTATGCGTGA	23077
rs574860311	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77058489	TTATATAAATTTCCA[A/G]AGATTACTTTCCCAC	23077
rs574895306	snp	C/T	0.00795532	0.062565	intron-variant	MYCBP2	GRCh38.p7	13:77160152	GCTCACCTCAACCTC[C/T]GACTCCCGGGTTCAA	23077
rs574901536	snp	C/G	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77229120	TAAGAACTTGGACTG[C/G]AATCTTGGCTCTTCT	23077
rs574908136	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77184501	ATCCTGTTTTGTAAA[C/T]GTCAGATCAAGATGG	23077
rs574909088	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77168882	TCATGATCTGAAGTA[A/C]ATCAGGTTTTACTTA	23077
rs574911634	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77277800	ATAATGAGAACCACA[C/G]CTCTAGTACTTCTGA	23077
rs574946518	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77199919	TCAAAGACCAAAAGT[A/C]GATAAAACCACAAAG	23077
rs574947613	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77298808	TAAAGAGAAAGAGAA[A/G]GATTAACAGTGCCAA	23077
rs574951660	snp	G/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77169347	CTTGCAGTGAGCGGA[G/T]ATCGCGCCACAGCAC	23077
rs574962435	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77301143	GTCAAGGCTGGGCGC[A/G]GTGGCTCACACCTGT	23077
rs574967961	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77224210	ATCATAATCACTCTC[C/T]TATTTAAAATATATA	23077
rs574973794	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77308572	CTGGTATTTAGTAAG[G/T]GCTAAACACATTTTT	23077
rs574977070	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77067249	GAACTTTACTTTATT[A/C]CCCCATATTTATTTC	23077
rs574996814	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77099938	GAGGCATTAGAGCCA[C/G]GCTGTCTGTGACCCA	23077
rs575012315	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77309632	CTGCTAAATATATCA[C/T]TAAATCCACTTTATT	23077
rs575022297	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77285648	AAAATTAGCCAGGCG[C/T]GGTGGCACATGCCTG	23077
rs575024323	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77243516	TACTCGGGAGGCCGA[A/G]ATGGGACAATCACTT	23077
rs575034099	in-del	-/ATA	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77050932	AAACAGAGCTTTCAT[-/ATA]ATGTTTACATAAAAC	23077
rs575036503	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77324418	ATAATTCTATCATTC[A/C]TTCAGAGCCGAAACC	23077
rs575043332	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77108949	TCACCCGCCTCATCC[C/T]CCCAAAGTGCTGGGA	23077
rs575057480	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77108656	ACGCAGCACAAAGAC[A/G]GCTAAAACCTAAACC	23077
rs575057811	snp	A/G	0.00159617	0.0282053	intron-variant, downstream-variant-500B	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77088037	GATCCTCCCTCCTCC[A/G]CCTCCCAAAGTGCTA	23077
rs575059989	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77256548	AAGAGCCACTCAAAT[C/T]CAATTAAAAAATGTG	23077
rs575062306	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77271825	TCAGCAGCGTGAAAA[C/T]GGACTTAATGCACAC	23077
rs575082052	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77161642	CTGCAAGCCATCCTC[C/T]GCACCCTTGGCACTT	23077
rs575084684	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77217451	AACAAATCAAATAAA[A/G]AAAACTAGGCTTTTA	23077
rs575111318	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77215328	TGCTTGACTATACAC[C/T]TTCAGACTTGGGGTG	23077
rs575128288	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77153795	AAAAATAGATGAAAT[G/T]TCCTATGTACCCTTC	23077
rs575138072	snp	A/C	0.000139272	0.00834364	intron-variant	MYCBP2	GRCh38.p7	13:77270570	AAAAATAATGAAAAA[A/C]CATTTTTAAATGTTA	23077
rs575154421	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77322328	CAATCCCCTCTATTG[C/T]TTTCACTAACATTGT	23077
rs575155848	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77210403	TTCACTGTGTTAGCC[A/G]GGATGGTCTCGATCT	23077
rs575160162	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77200567	ATACTCCTTGAGAAG[A/G]GCAACTCCAAGGCAC	23077
rs575176847	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075189	CTCTATCCTGGATGA[C/G]AGAGAGAGACCCGGT	23077
rs575195935	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77154608	CGTAACAGTATGAAC[A/T]TGGTATTAGAATGTT	23077
rs575208267	in-del	-/A/AAAAAAAAAAAAAAAAAAAAAAA	0.418315	0.190753	intron-variant	MYCBP2	GRCh38.p7	13:77243620	CCATCTCAAAAAAAG[-/A/AAAAAAAAAAAAAAAAAAAAAAA]AAAAAAAAAAAAAAG	23077
rs575213761	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075494	CTCTACTAATCTCAT[C/T]TGAATCCCTTCATTC	23077
rs575217261	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77210261	GCAGTGGTGCGATCT[C/T]GGCTCACTGCAAATT	23077
rs575220886	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77262304	GTATAGTACTCCAAG[A/G]AAAGATAAAGTTATC	23077
rs575225207	snp	A/C	0.000132884	0.00815011	intron-variant	MYCBP2	GRCh38.p7	13:77224430	TAACTCTGGATCTTC[A/C]AATGAAAAGTTAGCA	23077
rs575229591	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77119543	AAATACTGTTTTAAG[-/A]AAAAAAAAACTTACA	23077
rs575238156	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77154523	AAACATACCAGATAT[C/T]AAAAGAGATAATAAA	23077
rs575249515	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77316730	TAGATTCCTTTAATC[C/T]ATGGCTAGTATTTCT	23077
rs575252752	snp	C/G	0.00119737	0.0244387	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075677	TTGATTTCTTTTTGG[C/G]GGGGGTGAGGGGAAT	23077
rs575263924	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77233819	TGATCAAAAACAAAA[C/T]AAAAATGTCTATATT	23077
rs575286051	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77262925	AGTAAAGCACTAATG[C/T]CAAGTTTATGAAATG	23077
rs575287178	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77116439	TTTCCCAACACGGTA[C/T]AAAAAATACAATTCT	23077
rs575299736	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77114522	ACTTTAGTGTGTTCA[C/T]ATTCTCAAATGTAAA	23077
rs575311176	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77107023	TACGTTTATGTATTT[A/G]TATATATTTCTTTAG	23077
rs575314339	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77300990	AAGGAAACAAGAGAC[C/T]AGTAGTGCTTTAGAT	23077
rs575323466	snp	A/G	1.66624e-05	0.00288633	synonymous-codon	MYCBP2	GRCh38.p7	13:77262076	TTGCTGTTTTCATTA[A/G]CGCAAACTCTCGTCC	23077
rs575330231	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77126982	TTCCCATGTTGAAAT[A/C]ATTATTTATAAATAG	23077
rs575346856	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77145856	TTTTAAATAGCAAAC[A/G]AACAAAAAACAAACT	23077
rs575348838	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77115885	AAAGAAAAATAATCA[A/G]TCTGAACAAAGCTAA	23077
rs575377178	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77292033	AAGCTTTACAATGTG[C/T]ACCTGAGTTTCACTT	23077
rs575390069	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77130015	TTCACAGAAACGTTA[A/T]CCTAGAAAAATTAAC	23077
rs575390335	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77173093	AGAGAGACCCGGAGT[C/T]CAGGGCTCAGAGGTC	23077
rs575390377	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77142983	GGTTTTCGAAATTTA[A/T]CTGATCACAGAAACC	23077
rs575409640	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77185448	AACAATCAATATAAT[C/T]CAGTAATTCCCTATA	23077
rs575423933	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77103868	TAACCCCAGTATTTA[C/G]TGTTTGTTTTGTAGA	23077
rs575433510	snp	C/T			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77086328	AGCAATTATTCTCAC[C/T]GTCCCTCTTTTGAAA	23077
rs575444475	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77247631	AACAATCTTGAAAAA[G/T]AAGAACAAAGTACTC	23077
rs575451638	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77255439	AATCTAGAACATAGG[C/T]GTAAATGTACGCTCA	23077
rs575456234	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77292910	TGCAGTGAGCTGAGA[C/T]CGCACACCACTGCAC	23077
rs575462703	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77133433	GTGAAAACCTACTAT[G/T]AGCAAAGTGTAATTT	23077
rs575467964	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77248342	AACCCACAGACAGAA[C/G]TTTTTATTTTCAAAT	23077
rs575473634	snp	C/G	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77053039	GCTACTGAGAAGGCT[C/G]AGGTGGGAGGCTTGT	23077
rs575478158	snp	A/T	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77148149	TAGTAGAAATAATTT[A/T]AAAATTTGATACTAA	23077
rs575504428	snp	A/C	0.00835141	0.0640778	intron-variant	MYCBP2	GRCh38.p7	13:77068448	CCAAACAAAATATAA[A/C]AAAATACGAAATAAA	23077
rs575507112	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77101859	AGCATGTTATTAAAT[A/G]TTACTAAAAATTGTA	23077
rs575516337	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77249649	ATCCTCTGGCCTCAG[C/T]CTCCCAAAGTGCTGG	23077
rs575518333	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77257923	ACCGTTTATTTCTGG[G/T]GCAAAATAACTCAAC	23077
rs575520741	in-del	-/ATCT			intron-variant	MYCBP2	GRCh38.p7	13:77169482	TTTAATAATTAGCAG[-/ATCT]ATCTCTGCTTGTTAC	23077
rs575534806	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77147337	TCTGTTTCTTAATAA[A/C]AAAATAACAAAATGA	23077
rs575537053	in-del	-/TA			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77293098	CAAACTTCAAATCTC[-/TA]TGTCAGGCTCAGCTA	23077
rs575560279	snp	A/G			synonymous-codon	MYCBP2	GRCh38.p7	13:77261268	ATCGTGTCCAACTGA[A/G]AAGTGTACTATCTTT	23077
rs575585478	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77234452	TTAAATATCAAAGTA[C/T]CCTTCATTAAATGTA	23077
rs575617439	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77275870	GCGCCTGTAGTCCAA[A/G]CTACTCAGGAAGCTG	23077
rs575625714	snp	A/C	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228500	TGATAGAGTGAGACC[A/C]TGTCTCAAAAAAAAA	23077
rs575626615	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77165866	ACAAGAGTAGTCCTG[A/G]TTAACTGGTTAAGAA	23077
rs575634327	snp	A/C			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77079502	AAATAGATTAACATT[A/C]ATTCCTTGGAGAGCT	23077
rs575641682	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77059116	ATATCCACATTCTTA[G/T]TAATTGAGAAACCAA	23077
rs575645188	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77323652	TGGATTTTCCAAGAC[A/G]GCAGAGACTTTGTCT	23077
rs575645700	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77271826	CAGCAGCGTGAAAAC[A/G]GACTTAATGCACACA	23077
rs575650163	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77079059	TTCCTATAACTTTAG[C/T]CTCATTCTCACAAAC	23077
rs575654662	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77319939	GCAGATGTGCACACC[A/G]GAAGTTTATTGCGGA	23077
rs575664322	snp	G/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77237143	AAACTTACAATAACC[G/T]GAATGCCCATCAATA	23077
rs575684615	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77324689	TGGACCAAGGGCTAA[A/C]AAATCATTCACAAAT	23077
rs575684730	snp	C/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77069140	ACCATATTTTATCAC[C/T]GAAGGCACTTTTTCT	23077
rs575699045	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77216414	TAGGGGGAAATTTTG[A/G]TGAGAAGCAGGCATC	23077
rs575702531	snp	A/G	1.6601e-05	0.00288101	synonymous-codon	MYCBP2	GRCh38.p7	13:77156154	ATCATCCTTATTCAG[A/G]ATCAAAGATGTTTTC	23077
rs575728466	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77278502	CAGGCTATTGTGTGT[A/G]CTTCATAAGAGAAGC	23077
rs575745427	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77119535	AATTTTCTAAAATAC[C/T]GTTTTAAGAAAAAAA	23077
rs575771326	in-del	-/C	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77234528	ACAAAAATGCAAATA[-/C]CTCAAATTGTATGAA	23077
rs575801044	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77260375	ATGTCTTTGTCATAC[A/G]TAACTAGTATTGAAA	23077
rs575831718	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77112050	GAATGGTGCCTGGCA[C/T]GTGATAAATATTTGA	23077
rs575844016	in-del	-/AAG	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77250276	AAAGGCCTGTTATAT[-/AAG]ATGACCTATTTAACT	23077
rs575846202	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77169390	GACAGAACAAGACTC[C/T]GTCTCAAAAAAAAAA	23077
rs575864273	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77309756	CTTTTCATTCATCCT[C/T]TATAACACTACTAGA	23077
rs575873811	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77115753	AGTTAAACCATGCAC[C/T]GGTTGATGTGTGTCT	23077
rs575874680	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77052723	AGCAGTTCCCAATTT[A/G]TAATACTGTAGAACA	23077
rs575882168	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77157006	TAAAATCATGCAGGC[C/T]AGCATATTTTTTTCC	23077
rs575887922	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77119491	AATAAATGCTGTAGA[A/T]TATAGGAAAAAATTT	23077
rs575913037	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77252846	AATAATCATAGCTAA[A/G]ATGTACTGAGCACTA	23077
rs575914602	snp	A/G	9.89381e-05	0.00703273	synonymous-codon	MYCBP2	GRCh38.p7	13:77261244	TGCAACTAAAAGGGC[A/G]TGAGAGCCATCGTGT	23077
rs575919953	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77198793	AGATGTCTGTTTACA[C/T]ACTACATCAAAATGT	23077
rs575922628	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77163074	AAAGAGCTGCATATA[C/T]TACCATTGAATGGCT	23077
rs575928048	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77063998	TTCACTTCTTCCTAA[C/T]GTTGTCAGACTGCCC	23077
rs575940763	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77052225	TTTCTTTGAGACGGG[C/T]TCTCACTCTGTTGCC	23077
rs575948431	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77071524	ACCAAAACTTTTTTT[C/T]TGGAGTCCATTAGAA	23077
rs575959470	snp	A/C	0.00438332	0.0466095	intron-variant	MYCBP2	GRCh38.p7	13:77195367	TTTGGGAGGCTGAGG[A/C]AGGCAGATCATATGA	23077
rs575996095	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77145654	TAATGCATCTAATTA[C/T]TTTTTCCAAGTTTCT	23077
rs576011047	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77180871	GTTGCAGTAAACTGC[A/G]ATGGCACAACTGCAC	23077
rs576029165	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77136720	TCATTCTTTTGATTC[C/T]GAACTGATCGTTTTC	23077
rs576033116	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77126121	ATCATTTGTTAATAT[A/G]TTGTTTACACAAGGA	23077
rs576046118	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77201593	AACAGAATATACATT[C/T]TTTTCAGCACCACAC	23077
rs576054245	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77301816	AGATTAACAATATGT[A/G]TAAAATAATGCAATT	23077
rs576073058	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77253725	CATGCATATTATACT[A/T]CAATGTAACAAATAA	23077
rs576127908	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77281618	ATATTTGAAAGATAA[A/G]GAAACATGAAGCCCA	23077
rs576128086	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77289496	ACTTGACAAAAATCC[A/C]GTATCGATTCATGAT	23077
rs576132986	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77189399	ACCTGGGAGTAGTCC[A/G]ATGCAACACGTTATG	23077
rs576135131	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77134838	CAGTCAAATATGGTG[A/T]TTAAATAGAAAGACT	23077
rs576141715	snp	C/T	0.00716266	0.059414	intron-variant	MYCBP2	GRCh38.p7	13:77159446	GTCTAGATGACACCT[C/T]ATATACCATAATAAT	23077
rs576165429	in-del	-/A	0.00676609	0.0577691	intron-variant	MYCBP2	GRCh38.p7	13:77175380	GCAAACAGACATGAG[-/A]AAAAAAACCCATAGG	23077
rs576182013	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77213442	ATCATCATGCCACTA[C/T]ATTCTAGCCTGGATG	23077
rs576183330	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77165533	CTTAAATAGACTTGC[A/G]GCGGGGAGCGTTCCT	23077
rs576196990	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77063676	CTCATTAATGAAGAA[C/T]AGAAAATGACTTAAC	23077
rs576198304	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77268113	ATTAGAGGAAAAGTC[A/G]TACATTATTGAAAAT	23077
rs576219179	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77221151	ATCCTACCAATGTTT[A/T]ATCTTCATAAGAAAC	23077
rs576220401	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77106332	TGGTGTTCAATTTGT[C/T]GATTTCTTACTATGT	23077
rs576237517	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77282348	CCAGGAGGTGGAGGC[C/T]GCAGTGAGCCAAGAT	23077
rs576238332	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77092549	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA	23077
rs576250932	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77096784	AATTAGACAATACAA[A/G]TATAAAAGTTCTATA	23077
rs576254000	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77174225	CAATTTAATTATAAG[C/T]ATCCAGTTAGCAATT	23077
rs576259617	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77312958	TGTCCAAAGATGACC[A/G]AACACATTCTTCTCA	23077
rs576266736	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77214048	AAAAAGAAAGTTAAC[C/T]TTCAATGCCAAAATA	23077
rs576267351	snp	C/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77306417	TTCAACTTGATTTAG[C/G]GGAGAGATGAAAACA	23077
rs576279543	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77214183	GGTACCACAACACAT[G/T]CTGTTGGCAATTCTG	23077
rs576289366	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77211394	AAACCCATAAAGTAG[C/T]ATTATCTCCATTTCT	23077
rs576301203	snp	C/T	0.00557542	0.0525036	intron-variant	MYCBP2	GRCh38.p7	13:77049354	TTTGACATGAGCAAA[C/T]GGTAAAAAGTAGTCA	23077
rs576301439	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77305443	CAATGGCAACAAAAG[A/G]TCATAAATTGTATAA	23077
rs576304969	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77168177	GTTTAGCATTATATA[C/T]CACACTATACTTGTA	23077
rs576345033	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77245650	TAGGAGAAATACCTA[A/G]TGACCGGTTGACAGG	23077
rs576353157	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77298535	ACGAGTATTTTAAGA[A/G]AAAGAGAAAGTATAA	23077
rs576360310	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77097129	ACCCTTTGGGTAACA[C/T]ATAATATTTTTTAAA	23077
rs576376096	in-del	-/TCT			intron-variant	MYCBP2	GRCh38.p7	13:77278674	ACTTTAGAAATATTC[-/TCT]TAACAATTTTGAAGT	23077
rs576390390	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77152907	CGTCTCTACTAAAAA[C/T]ACAAAAAATTAGCCA	23077
rs576419162	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77191987	ATGCAAGCAAATATA[A/G]TTATTTATGTTATGG	23077
rs576424959	snp	C/G	0.00279162	0.0372561	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77328989	TAGCACAGGGTCTAG[C/G]CCTGAACAGGAGGGA	23077
rs576438581	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77328118	GTACTGTATCTTTCA[G/T]CTATGTACTAGTTCT	23077
rs576461415	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77163662	CTCTGTTCTGCTTCA[A/G]TGAAAAATTCTTCTA	23077
rs576482400	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77246410	ACAAGAATTCATTCT[C/T]TGAGGTCAGGATTAC	23077
rs576491954	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77214095	ACTTTGAGGATCAGA[A/G]CACCAACTAAAGGCA	23077
rs576501502	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77238413	GTTTAATTTTCCTTA[C/T]GAAACAGAGTGCTGA	23077
rs576506767	snp	A/C/G/T	0.000114442	0.00756373	intron-variant	MYCBP2	GRCh38.p7	13:77089075	TTCATAGGCAGTGCA[A/C/G/T]ATATATTTAAGATAA	23077
rs576509661	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77222221	GCATCTAACACCTGT[A/G]ACAGTAATTGCTCAA	23077
rs576528044	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77190769	AAAGACATTCTTAAG[C/T]TGATGCACATAACAA	23077
rs576532538	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77221698	CTAAATAACAACAAC[A/T]ATAGCCACGATGATA	23077
rs576534108	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77065790	CACACAAATTAACTG[C/G]AAAATTTGAAATGAA	23077
rs576537475	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77130763	AGTGGGACAGACTTT[C/T]TGACATAAAACAATA	23077
rs576564463	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77248633	TGTTAAGAAGGATGT[A/G]GAGAAACTGGAACAT	23077
rs576582917	snp	A/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77183662	CTTCAAGCAATTCTC[A/G]TGCCTCAGCCTCCCG	23077
rs576594395	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77253956	AAGGAGGTTTTAAAC[A/T]CATTTATAACAATGA	23077
rs576608510	in-del	-/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77325221	CTGACTTACAGCCTC[-/G]GTCCCTTTCATAATG	23077
rs576614984	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77130292	AATTATAAGTCATTT[C/T]AGATAATGAAACTTT	23077
rs576641197	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77214725	ATACTTAGGTGATAT[G/T]GTGTAGCCTATTGCT	23077
rs576649909	snp	G/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77089696	TTTATATCCCCAAAG[G/T]TTTATTATCTACTTA	23077
rs576657439	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77066412	GGAATATAAATTCAC[A/T]GTATCACTAAGCACA	23077
rs576668028	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77255005	ATTCATCTGTTGATG[A/G]ATACTTAAGTTGATT	23077
rs576668695	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77269771	TTAACTGAGTTGTCC[A/G]GTCATACAGCTAGTA	23077
rs576686113	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77287482	GAGAGCCACTGCGCC[C/T]GGCCTACAATACATG	23077
rs576697672	snp	A/G	1.65181e-05	0.00287381	missense	MYCBP2	GRCh38.p7	13:77098135	CATCTCCTTTGAAAA[A/G]AAAACTCGATTTTTC	23077
rs576701908	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77245807	AAAAACATTCACACA[A/T]TGGAAAGGAAAAAAT	23077
rs576703696	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77254625	ATATTCTAAATTCTC[C/T]CTTCTAGCTATTTTG	23077
rs576723449	snp	C/T	0.000399281	0.0141238	missense, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081869	AGCCAGACTGTATAC[C/T]GATGCTAAAACTCTC	23077
rs576731961	snp	A/G	5.82123e-05	0.0053947	intron-variant	MYCBP2	GRCh38.p7	13:77064575	AACACGCAATGATAC[A/G]CACCAAATTTAAAAC	23077
rs576754228	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77120332	GCTAGTCCAAGGGAG[C/T]AAAAAAAAATCTTGT	23077
rs576761138	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77320290	GGAACATGTGCCTGA[A/T]AGCGGGATCTGAAAG	23077
rs576761993	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77113812	TAAAATGATTTGTAT[C/T]TGTAGGGATGCTGGA	23077
rs576771883	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77290409	ACACAAAAACCAGTA[A/C]ACGAATGTTCGTAAT	23077
rs576797526	snp	A/C	0.00279162	0.0372561	intron-variant	MYCBP2	GRCh38.p7	13:77229706	GTTTTTAAAATAAGA[A/C]AACTGAAGCCAAAGA	23077
rs576806307	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77222318	TGCTCTTTGCAAGTA[C/T]GATATTAGTCATTAA	23077
rs576810141	snp	C/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77139450	GTGCAGATTAAGCAT[C/G]TAGTTTTTGCAGAAA	23077
rs576861391	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77065653	TGAGGAGAATGAGAA[A/G]CTTCCACTTTCGAGA	23077
rs576864092	snp	A/C	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77268973	TTCTTTATCCTTATA[A/C]AAAGGAACTTGGGCT	23077
rs576865666	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77246556	GGAGGAGGAGGAGGA[A/G]CAGGAGGAGAAGGAG	23077
rs576868228	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77055992	GAGCATGAAAATTCC[A/G]TTTTATTAGCTTTAT	23077
rs576868706	snp	C/T	5.01316e-05	0.00500632	missense	MYCBP2	GRCh38.p7	13:77166350	ACACCAAAACCATAG[C/T]AGGCCACCCAGAGGA	23077
rs576871959	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77138702	CTTCAACTAGAATAC[A/G]ACGGAGCACCACAAA	23077
rs576878020	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77277165	TCAAAGTAGGAAATA[C/T]GACATCCAAGTCTTC	23077
rs576878976	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77176345	GTACAACATTAGGTA[C/T]GTAGTAGGTACTCCA	23077
rs576881533	snp	C/T	0.000297142	0.0121854	missense	MYCBP2	GRCh38.p7	13:77121477	GGAGTTTGAGAATTC[C/T]GATCCAGAAGAGCTT	23077
rs576895885	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77268163	AAACATAATTAGGTA[C/T]ACTAAACAGGACAGT	23077
rs576906899	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77320771	CGCCATATACAATAT[A/T]CTTGCTAAAAAATTT	23077
rs576913457	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77051638	ATAAAATAAAAATAT[C/T]GCCCAAAGGAAATAA	23077
rs576927926	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77261831	CAATTTGTAAAAAGA[A/G]CAATTATTTGTGAAG	23077
rs576932607	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77283168	TCTGATGCAATCATG[C/T]AAGTCTGATGATATT	23077
rs576932777	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77275508	AATCTCATATGTCAC[A/G]TCTTCAGGGAGCCTG	23077
rs576945380	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77207291	GAAAGGAAGCACAGA[C/T]AGAATGGATGTGGAT	23077
rs576954759	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77129486	AATTAAGAGCCAGAC[A/G]TTGTTATAAAGCTTA	23077
rs576992266	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77313882	CGAACAAGATATATA[A/G]ATGGCAAATAAGCGT	23077
rs577020065	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77199313	CGGGTCACTCCCACC[C/T]GAATACTGCACTTTT	23077
rs577040292	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77277654	GTGTACTCCTCAAAC[C/T]AGCATCTGTATCACC	23077
rs577042614	snp	C/G	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77200767	AAAAGAATTTCCAAC[C/G]CAGAATTTCATATCC	23077
rs577074227	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77153581	CTATGTGTGTATGCA[A/C]CATGAACCTTGAAGT	23077
rs577077830	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77145751	AACAGAATTACTTAC[A/G]GGCTGAAAAATTAAG	23077
rs577080038	snp	A/G	0.00755907	0.0610114	intron-variant	MYCBP2	GRCh38.p7	13:77120293	GAAGTAAGCGAGCAG[A/G]TGATACCCAATCCTA	23077
rs577100366	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77208225	CAGGGCACAGATCCT[A/G]CTGTGGCTTGTCTTT	23077
rs577110837	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77198920	GAAAGGACTGAGATA[C/T]AGTCTTTCTTCAGTG	23077
rs577114451	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77271168	CTATATCAAATAATT[C/T]CAATATCTAAGGACT	23077
rs577118377	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77161708	CTCCAGAGTCAATTA[A/C]CCACCAAATACATAG	23077
rs577131164	in-del	-/AAC	0.226843	0.248925	intron-variant	MYCBP2	GRCh38.p7	13:77243177	AGATGATTGGCCAAA[-/AAC]AACAACAACAACAAC	23077
rs577148958	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77270614	AAGATACTTTGGTAA[C/T]ACATCATCATTCATA	23077
rs577165522	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77191237	TATACGTGAAAGTTA[C/T]TTTAAAACAGCAAAA	23077
rs577168332	in-del	-/G	0.00478562	0.0486817	intron-variant	MYCBP2	GRCh38.p7	13:77054404	ATTTTAGATCTAGAA[-/G]TATTAATTAGCAGCA	23077
rs577176038	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77091003	AACAAATTTAGAAAC[C/T]ATTCTTTTCGTGAGC	23077
rs577177026	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77049590	AACAAATATGACTAG[A/G]TAGTCTCATTTTCCC	23077
rs577179446	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77284883	AACTGAGGCACGGAT[A/G]TGTCAAATAACTTCC	23077
rs577195477	snp	C/T			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77079011	TATGGTCCTTCCTGA[C/T]TGACCCCACCCCATC	23077
rs577216073	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77050684	ACAGAATCCTTTTAA[A/G]TGGTTCTGTAATATT	23077
rs577216196	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77146471	CTTTTGAGTACATTA[A/C]AATTTTAAAGTTTTC	23077
rs577222410	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77284637	AAGTTTCATTTGCTT[A/G]CATAATTTTTTTAAT	23077
rs577232728	snp	C/G			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076398	CAAATTTCATGAAGA[C/G]GATAAATCGTAAAAA	23077
rs577256473	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77082799	AGATTGCTACAGTGA[C/T]AATTTAGGGCACTAA	23077
rs577257489	snp	A/C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77306880	AGATGGTGGGATTTT[A/C/T]GGAAAGATTGCAACA	23077
rs577259029	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77298651	TCTATGGTATCGACA[G/T]GAGTGCATTTAAAGC	23077
rs577268942	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77249969	TGGCTCACGCCTGTA[A/G]TCCCAGCACTTTGGG	23077
rs577274961	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77280025	CCTAGCCAATTACCT[A/G]GCATATGGTAGGCAC	23077
rs577290646	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77239438	TCTTTTCTAGCACAG[C/T]GCCAGAGAAGAGCCT	23077
rs577299825	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77105825	GCTCATTTGAAGTTA[A/G]TATTGTTTGCTTACT	23077
rs577301707	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77069393	TTTGGGAGGCCGAGG[A/C]GGGCGGATCATGAGA	23077
rs577307034	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291841	GTTAACGCTGCAGGC[A/G]TGATTGCTTACTCCT	23077
rs577318065	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77259026	TGAGGAGGCTGAGGC[A/G]AGTGTATCACTTGAG	23077
rs577324220	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77135128	TTTAACTAGAAAAGG[C/T]TGAAGAGATAGACAC	23077
rs577327171	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77168978	ACTCTTATCCTTTAA[C/G]ATTGCTATTGTTATT	23077
rs577327909	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77058012	CCAGCTAATTTTTTT[A/G]TATTTTTGTAGTAGA	23077
rs577328607	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77192102	TTTTAAACTGATATT[A/T]AAAAACATTCAAATT	23077
rs577338417	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77103503	AAGGTCGAATTAATT[A/G]ATTTAGATTAATATG	23077
rs577347118	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77123626	CACAGAGATATTAGG[C/T]TAACTTGGTCAAGGT	23077
rs577362564	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77113974	TCCCACAGGTCCTCA[A/T]TCCTAAATCAAGTGC	23077
rs577364672	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77322423	CTTGGCATCACTTTC[C/T]TTTTTACCATATAGT	23077
rs577403476	snp	C/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77074011	CCCACCGCCCCCCCC[C/T]CTTTTTTTTTTAAAG	23077
rs577405549	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77184411	CTAGCATATGATCTA[C/T]CTTAGTGAATGGTCC	23077
rs577428871	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77221053	GTCATATGGTTGGTA[A/C]GAAGTGAAGAGCTGA	23077
rs577432150	snp	C/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77209359	ATCCAGAAACAGATT[C/G]CACACTGCCAATTTT	23077
rs577444150	snp	C/T	0.00318978	0.0398085	intron-variant	MYCBP2	GRCh38.p7	13:77183771	TAGGCTGGTCTCGAA[C/T]TCCTGACCTCAAGTG	23077
rs577454086	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77263210	TGAGATCATTCTATA[G/T]TTACCTTGAAAATCT	23077
rs577458523	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77298446	AGCTAAAAGCTCCAA[A/T]AGTGCAGGGGCCCTG	23077
rs577458804	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77268508	TTTCAGGCTGGGGGC[A/G]GTGGCTCACGCCTGT	23077
rs577463226	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77058589	AGGCTTCTTAACAAA[A/G]TTTTTTTTTTTTGAT	23077
rs577463332	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77151799	TTCTGAAAAATACTT[C/T]TTAGAAATATTTCCC	23077
rs577464733	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77187090	GCTGGGATTATAGGC[A/G]TGAGCCAATGTGCTA	23077
rs577497828	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77295969	CAAGTCCCAGTTTAC[A/C]AGCTAATTTTACTCA	23077
rs577500475	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77314943	AAAAATATTTTTTTT[A/T]AAAAAGGAGGGAGTT	23077
rs577502158	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77223528	GTAGAATACAAACTC[A/G]GCTGCTGTAATGAAA	23077
rs577511367	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77274495	AGGGAAAGGGAAGGG[A/G]GAGAAGGAGGAGAAC	23077
rs577515382	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77164771	TGTTCATTCATGACT[C/T]TGGCCCACTTTGTCC	23077
rs577546255	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77273724	CGGAACATTATATGC[A/G]TATATTTATTTATTT	23077
rs577549359	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77255111	TCTTTTTGATACATA[G/T]ACCCAGAAGTGGAAT	23077
rs577564050	in-del	-/CTTA			intron-variant	MYCBP2	GRCh38.p7	13:77255311	ATGCACTGTATGTGT[-/CTTA]CTTTACTCATCTGCT	23077
rs577566979	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77158326	TCCCTCAAAAATAAA[A/T]GCCTTGTCAGAGATC	23077
rs577573033	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77312154	CCACCTAAAATATCC[C/T]TTAGGAATGAAAGTA	23077
rs577577827	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77216129	AAAAAATGAAGGGGC[A/G]TGTCACAAGAATACA	23077
rs577584121	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77285403	TCTCAATCTCTCCTA[C/G]TTAAGCATAAGAAAT	23077
rs577599353	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77319625	AAAGCCATCTGATGA[C/T]TGTCCTCATAATTAA	23077
rs577609623	snp	A/G	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77048544	CTATTCCAGTTCTCT[A/G]AATGAATGGATGAGT	23077
rs577615260	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77215449	TTAGACATATCTGGG[A/G]ACTAAGTGAGAAATA	23077
rs577620803	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77283402	TGGTTCTTATCCCTA[C/T]AAGACAATGCTTTCT	23077
rs577638931	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77311082	TTTGGTTGTTTTTCT[C/G]CTTTCACTAACAGCT	23077
rs577651391	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77157798	AAATATTAACTATCA[C/T]TTTATATTTCAGCAA	23077
rs577652914	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77179362	TTTCCAAACCAATCT[A/G]CTGTCTGTTTTTTAG	23077
rs577665640	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77197554	AGATACAAATTTGGG[G/T]ATTATGGTATGCTGA	23077
rs577674312	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77295452	TATCATTTCATCCCC[A/G]GATCCATCTGTGTCT	23077
rs577707744	snp	A/C	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77287226	AGTCTCACTCTGTCA[A/C]CCAGGCCGGAGTGCA	23077
rs577723637	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77133011	ATCCTCATTCAACCA[C/T]TAAGGTTATAAGTAT	23077
rs577724338	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77085657	GCATGGCATATGAGT[A/T]TAGTGTTCGCCATTT	23077
rs577726588	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77196043	ATTGGGAGTAAGTCT[A/G]TGGTTGGGAATTGAA	23077
rs577729906	snp	A/G	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77171863	TAAGATCAGTTCTCC[A/G]AGGAACTCATATTTA	23077
rs577756369	snp	C/T	0.00199481	0.0315187	utr-variant-5-prime, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326813	GCCGCCTCGTCCCCG[C/T]GGGCCGGGCGGGCAG	23077
rs577771561	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77046515	CTGACATAAGAGAAG[G/T]AAACCATGATGGATA	23077
rs577783143	snp	A/G	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77069817	AGCTTGCAGTGGGCC[A/G]AGATCGCACCACTGC	23077
rs577801185	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77126270	GCTTTGGTTGTATTA[C/T]ATTAAAAATGAGTAT	23077
rs577823602	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77212213	TGTAAACAATCTAAT[A/T]TTCATAAAGTTAAGG	23077
rs577825766	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77196172	GAAACAGCAAGTGAA[C/G]AGGTACTGAGATTTG	23077
rs577829991	snp	A/T	3.39213e-05	0.00411819	intron-variant	MYCBP2	GRCh38.p7	13:77189066	AAGGCAGTAGACACA[A/T]ATAAAATTATGTTAG	23077
rs577837433	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77187645	CATGATATATAATAC[A/G]AAATTTTCTAAAAAA	23077
rs577885632	snp	G/T	0.00119737	0.0244387	intron-variant	MYCBP2	GRCh38.p7	13:77118677	GACCGAATTTTGCAA[G/T]CTTTTTTTTTTAATG	23077
rs577890890	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77160490	GGAAATAAGTAAAAT[A/G]TAAAGCACTAGCCTT	23077
rs577896811	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77318516	ATCCCAGCACTTTGG[A/G]AGAACGAGGCAGGCG	23077
rs577903934	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77080012	TCTGAGGGAGAGTAT[C/G]TCCTTGCTTAAAATG	23077
rs577904646	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77310092	ACTCCAGCCTGGCAA[C/T]GGAGTGAGACTCCGT	23077
rs577905687	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77327165	TTTTCCTCCCCACCC[C/T]CTCTCCGCCACCACT	23077
rs577933320	snp	C/T	0.00119737	0.0244387	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77077885	CATAATATGTAACTT[C/T]ACACTTGTGATTCCT	23077
rs577933854	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77203637	ATCACACTACCTGAC[C/T]TCAAACTATACTACA	23077
rs577939387	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77226126	AATGGCCTATTCTTA[C/T]TCATGTTTCCTGTGC	23077
rs577960529	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77258878	ATTTTTTGCAGGTAG[A/T]AAAAAACAAAAAGAA	23077
rs577961910	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77226723	CCAGGTGAGACAAAA[C/T]CTACCTACATTATTA	23077
rs577974334	snp	A/C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77220032	AACTGGTTGAATCTG[A/C/G]AAATTAAGTATCAAT	23077
rs578017590	snp	A/C	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77100825	TAACAGATGGGGCTA[A/C]GTTTTGAAAAAAGGG	23077
rs578043388	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77109409	AGCTGAGACAGTAAT[A/G]CTCTCCTCCTGCTGT	23077
rs578066549	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77103148	GACGAACGGAAACAT[C/T]TTTAATGACACTCCT	23077
rs578078074	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77105311	CTCCTGGAAAAAAGT[C/T]TGAAGGCAAAATGGC	23077
rs578083957	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77144708	GCCTACTCTCCAAAA[C/T]GCTTGAATTTCACTT	23077
rs578094570	snp	C/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77288738	TAGACACACTGTAGA[C/G]TCTCAATGACCTACT	23077
rs578101276	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77297673	GAAAAAAAGTAATGG[A/G]TTTGATTTTGAAGAT	23077
rs578116188	snp	A/C			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228948	ATGCATATAACAGAA[A/C]CTACCACAGAACACA	23077
rs578133962	snp	A/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77251718	GTTCCCCACTCTAGA[A/T]CATCCTCCTACTGCC	23077
rs578189199	snp	A/G/T	6.64213e-05	0.00576254	missense	MYCBP2	GRCh38.p7	13:77181822	CCATCATACGCAATC[A/G/T]GGAAGATGGAAGTCA	23077
rs578189937	snp	A/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77244747	TACAGAATGGGAGAA[A/T]ATTTTTGCAATTTAC	23077
rs578190856	snp	A/G	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77128853	AAAAATAAAAGAGCC[A/G]TAAGGCCAGGACACT	23077
rs578191844	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77136846	TCTCTTTTACAGAAG[C/T]AAGCTCTCTAAGGTG	23077
rs578206646	snp	C/T	0.000798403	0.0199641	intron-variant	MYCBP2	GRCh38.p7	13:77181076	TATGTAGTTTTATAA[C/T]TTCTACTGTATTTGT	23077
rs578226037	snp	G/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77289569	TCAACTTGATAAAGG[G/T]TATCTACAAAATAAC	23077
rs578237029	snp	C/T	0.00159617	0.0282053	intron-variant	MYCBP2	GRCh38.p7	13:77244093	CTCTTTAGATCACGA[C/T]TGTTCATTTTAAAGA	23077
rs578238376	snp	C/T	0.000399281	0.0141238	intron-variant	MYCBP2	GRCh38.p7	13:77282462	AAGTTTCTGAGTTCC[C/T]TGCCTAACAAATTTA	23077
rs578262618	snp	A/T	0.00199481	0.0315187	intron-variant	MYCBP2	GRCh38.p7	13:77088708	GGAACACTTAATACT[A/T]TTAATTGGCTAATGC	23077
rs745308161	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77229353	ACAGATGAAAAAACT[A/G]AGGCTTGAAGGGTTA	23077
rs745323880	snp	A/T	6.65192e-05	0.00576673	intron-variant	MYCBP2	GRCh38.p7	13:77261164	CATAGTTGATCACTC[A/T]ACTTACTTGATTCTC	23077
rs745342364	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77244518	CAAAAATTAATTCAA[C/G]ATGGATTAAAGATTT	23077
rs745357842	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77189143	GAATGGGAAAATAAA[C/T]TATATATTTAAATTT	23077
rs745363116	snp	G/T	1.65504e-05	0.00287662	missense	MYCBP2	GRCh38.p7	13:77140064	CATCAATAAAAGTGA[G/T]AGTTCCATTGACTTT	23077
rs745374512	snp	A/G	6.668e-05	0.0057737	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087465	AAATATGCACAATCA[A/G]AACAAAAATTTCATT	23077
rs745375644	snp	A/G	1.64885e-05	0.00287123	intron-variant	MYCBP2	GRCh38.p7	13:77233147	TAGGTGATAAGGAAG[A/G]CCAAATACCTTTGTG	23077
rs745381252	snp	A/C/G	3.35899e-05	0.00409805	intron-variant	MYCBP2	GRCh38.p7	13:77070738	AAAAGAAAAAAAAAA[A/C/G]AAAGAATGAAGTGGT	23077
rs745392467	snp	C/T	1.83761e-05	0.00303112	intron-variant	MYCBP2	GRCh38.p7	13:77205642	TCCTTGAAATTAAAA[C/T]GTCCTATGGTATTGA	23077
rs745421479	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77123453	ATAAAATTTCCCAGG[A/T]TAAAACTTGATCCTT	23077
rs745424300	snp	A/G	1.92469e-05	0.00310211	intron-variant	MYCBP2	GRCh38.p7	13:77278929	ATTTAAAAGGAAAAA[A/G]TATATATACTTTATG	23077
rs745428003	snp	C/T	1.6486e-05	0.00287102	missense	MYCBP2	GRCh38.p7	13:77045400	GTGTGGGCATTTCTG[C/T]ACACTCCACATCCCA	23077
rs745430273	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77216670	AATGAAGAGGATTCT[A/G]TTTTTCAAAACAGTA	23077
rs745444062	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77151545	TATTAAATAATTAAA[C/T]TTTGCAACTCACTTT	23077
rs745452631	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77173402	GTAGTGCTTATGTAA[C/T]AGAAAGCTTTTCTTG	23077
rs745458319	snp	C/T	1.76386e-05	0.00296967	intron-variant	MYCBP2	GRCh38.p7	13:77058442	TGTTACACAAGTATG[C/T]AAAAAAGCACACATT	23077
rs745469292	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77308118	GCCAGTTAAGTTCTC[C/T]ATCAAGGTACATCTA	23077
rs745482340	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77101181	GGGAATCTAGACAAA[C/T]AATTAGTAAGTCTTT	23077
rs745484913	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77257594	ATTTTGAAAAGAACA[A/C]GACTTTTCACTATGT	23077
rs745485771	snp	C/T	1.65932e-05	0.00288034	synonymous-codon	MYCBP2	GRCh38.p7	13:77260588	GGATTGCCGTCTGCT[C/T]TTAGCTTTAAAAAAG	23077
rs745493124	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77115722	AGATAATAATGCTCA[C/T]AGAAATGCTAGATGA	23077
rs745510691	in-del	-/C	1.95227e-05	0.00312425	intron-variant	MYCBP2	GRCh38.p7	13:77181944	AAAACAAAAATATGG[-/C]CCCCCAACCAAAAAA	23077
rs745512154	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77275124	AGGGTATTGGCAAAC[A/G]TGACAAAGAATGTCT	23077
rs745537934	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77188073	AGACTCTGCCTCACC[-/A]AAAAAAAAAAAAAAA	23077
rs745538086	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77258918	ATGTTTAGTAAACTG[C/T]TACCCAGTTAAAGAT	23077
rs745540652	in-del	-/T	1.68838e-05	0.00290544	intron-variant	MYCBP2	GRCh38.p7	13:77194109	AATAAATTTTTAATA[-/T]TAAGTATGCAAGAGT	23077
rs745549147	snp	C/T	1.85644e-05	0.00304661	intron-variant	MYCBP2	GRCh38.p7	13:77051944	AACACATCTAGATTA[C/T]AGCAGGAAAAAAGAA	23077
rs745562250	snp	A/G	0.000148421	0.00861326	synonymous-codon	MYCBP2	GRCh38.p7	13:77096339	AGCAGCCTGTTTTTC[A/G]CGGAGGTATTTTTCT	23077
rs745564444	snp	C/G	0.00225044	0.0334687	missense	MYCBP2	GRCh38.p7	13:77171534	GGTCCTTAGAGGCTC[C/G]AACGACAGTGCTTAC	23077
rs745574251	snp	A/C			upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77328749	ATCAGACAGCCCTGG[A/C]ATTGGATCCTGACTC	23077
rs745584235	snp	C/T	9.93624e-05	0.00704779	missense	MYCBP2	GRCh38.p7	13:77181792	TGTTTAACAATTGAT[C/T]GTAGTAATACTTCTC	23077
rs745590695	snp	A/G			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77080462	CTGGCAGTTAGTGCT[A/G]TTTCTTTCTTGGTTG	23077
rs745600920	snp	C/T	0.000112857	0.00751105	intron-variant	MYCBP2	GRCh38.p7	13:77243998	ACAACTGAGATATTC[C/T]TAATTTGTCTTTAAA	23077
rs745606229	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77131037	AATTGCCAATAAAAT[C/T]AATTCTGTATATGCT	23077
rs745610646	snp	A/C	1.67497e-05	0.00289389	missense	MYCBP2	GRCh38.p7	13:77263980	ATCAGTGAATAAAAT[A/C]TTTTGACCTTCAGTG	23077
rs745616230	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77114265	CACACCAAGAATAGA[C/T]TGCTCTCTTTTAGAG	23077
rs745624474	snp	A/C	1.65329e-05	0.0028751	intron-variant	MYCBP2	GRCh38.p7	13:77125311	AAGCTTAATTGGAAT[A/C]AATCACAAATTTAAG	23077
rs745630614	snp	C/T	7.0039e-05	0.00591731	synonymous-codon	MYCBP2	GRCh38.p7	13:77055741	TGGATCAAGTAGGTC[C/T]TTTAGTACTATGTGA	23077
rs745636591	snp	C/G	3.30338e-05	0.00406397	missense	MYCBP2	GRCh38.p7	13:77064709	GCATTTTTTGTCACT[C/G]GGGACCAAGCTTCTG	23077
rs745641500	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77162818	TGTGCCACCATGCCC[A/G]GCTAATTTTTGTATT	23077
rs745654163	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77220983	CCATGCTGGAAAAGA[A/G]CAACTTTGGGCAGTT	23077
rs745671550	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77065472	GCCCTCCTAGAAATA[A/T]TACAATGTGTGGAAA	23077
rs745676820	snp	C/T	1.65081e-05	0.00287293	synonymous-codon	MYCBP2	GRCh38.p7	13:77093290	CATTTCATCCTGGAA[C/T]AGATTGTCATCTTGA	23077
rs745677034	snp	C/T	1.65362e-05	0.00287538	missense, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081603	GGCTTGAAGTTTTTA[C/T]GTCAACAATGCTGGT	23077
rs745683435	snp	A/G	6.62822e-05	0.00575645	missense	MYCBP2	GRCh38.p7	13:77177953	GAATTAAGTCCATCA[A/G]CCTGTGAACAATAAA	23077
rs745683790	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77306668	ATAGGCTAGGTAGGC[C/T]AGGGAAACTCAAGCC	23077
rs745687570	snp	C/T	1.64857e-05	0.00287099	synonymous-codon	MYCBP2	GRCh38.p7	13:77189011	TTCACTGGTTTGCTG[C/T]TTGCCTTTTGAAGCA	23077
rs745697601	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77321838	TGTCTTATAAATTTT[A/T]ATAGGGCCAATGGTT	23077
rs745707562	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77263528	ATCCTTTATATTAAT[A/C]GTAACAGACACAAAA	23077
rs745719997	in-del	-/AAATCTACCTCAAAAAAGT	1.6495e-05	0.0028718	frameshift-variant	MYCBP2	GRCh38.p7	13:77098864	TTCACTAGCAGATAA[-/AAATCTACCTCAAAAAAGT]ACTTTCTGTGCCCCT	23077
rs745741986	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77300598	TTTGATAAACAGGCC[C/T]ATATCAGAAAGGAAA	23077
rs745743708	snp	A/G	1.64749e-05	0.00287005	synonymous-codon	MYCBP2	GRCh38.p7	13:77251234	GACAGTGCAAACCAT[A/G]CACTGCTCCAGCTTC	23077
rs745759160	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77195915	TAATTTGTCCCCAAT[A/C]TGACTCCTGTATTTA	23077
rs745759516	snp	C/T	1.71528e-05	0.0029285	intron-variant	MYCBP2	GRCh38.p7	13:77099031	GTATGGTCCATTTTA[C/T]AGTGAAACTTATTAA	23077
rs745761977	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77284603	TCTCATTCATCAGGT[C/G]ATTGCACTGATTCTC	23077
rs745766295	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77109121	CCATTGTTTCCTTTA[C/T]TCTTATGTGGCAGGT	23077
rs745766831	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77093845	TTGAAAAATATTAGA[C/T]ATATGAAATTTTCTG	23077
rs745766890	in-del	-/TAAAC			intron-variant	MYCBP2	GRCh38.p7	13:77226935	GTACAGATTACAGAT[-/TAAAC]TAAATGCTACAATAA	23077
rs745767496	snp	A/G	1.6669e-05	0.00288691	intron-variant	MYCBP2	GRCh38.p7	13:77062748	TTAGGAAAGACTTAT[A/G]AAATGCTGACTGTGA	23077
rs745774262	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77179305	TGCTGATTATTAAAC[A/G]TTCATTTGAATGATG	23077
rs745784040	snp	C/G	1.65157e-05	0.0028736	missense	MYCBP2	GRCh38.p7	13:77206729	AAGTTCAGGACTTAG[C/G]ATACTACATCTGGAC	23077
rs745805923	in-del	-/ACAC			intron-variant	MYCBP2	GRCh38.p7	13:77166971	TCAAAGACAAAACAC[-/ACAC]ATACACACACACACA	23077
rs745809247	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77144235	GAGAGAGTCATGAGG[C/G]CTACAGTGCCTGGGC	23077
rs745811015	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77184330	TTTTACTGTAATTCT[A/G]CTGTGGTCTGAAAAT	23077
rs745815014	snp	A/C	1.66651e-05	0.00288657	intron-variant	MYCBP2	GRCh38.p7	13:77263883	TAAATAATTTAAGGA[A/C]AAGGAATTCCATTTA	23077
rs745842617	snp	C/G			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77077048	GGGCAACATTTATAG[C/G]CAGAAATTTCTGTAA	23077
rs745842807	in-del	-/T			intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77074013	CACCGCCCCCCCCCC[-/T]TTTTTTTTTAAAGAA	23077
rs745847403	snp	C/T	6.61376e-05	0.00575017	synonymous-codon	MYCBP2	GRCh38.p7	13:77098067	CACAGCTCTGGCACA[C/T]TCGGCCACAGAAGGA	23077
rs745848495	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77236746	ATTAAAAAGAATAAC[C/T]AAACCCAGGTGTGGT	23077
rs745848991	snp	A/T	1.87827e-05	0.00306447	intron-variant	MYCBP2	GRCh38.p7	13:77186080	TAATCCAGAATATGA[A/T]AAAACAGACAACAAT	23077
rs745854808	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77094701	CTGTCGCTTGCCTGA[A/C]AGATTTCTATTTATC	23077
rs745855237	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77320489	GAAATAACAGAATTA[C/T]TTTTTAATTCATCAT	23077
rs745857540	snp	C/T	1.66084e-05	0.00288165	missense	MYCBP2	GRCh38.p7	13:77146181	TAGGAGTTGGTGATG[C/T]AAAACGTAGTTCTTC	23077
rs745878280	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77069026	AGCTAAGGGAGCCAC[A/T]ATAAAAATGGAAATA	23077
rs745886788	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77271080	CTTTTTATATTCTCA[A/C]TACTTAATCATACTT	23077
rs745890025	snp	G/T	1.80049e-05	0.00300035	intron-variant	MYCBP2	GRCh38.p7	13:77273464	AAGCAGATATAAATA[G/T]GAAATACCTGAATAG	23077
rs745891546	in-del	-/ACAC			intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326244	TAGGCAGGCAGACAC[-/ACAC]ACACACACACACACA	23077
rs745902491	snp	C/T	3.02174e-05	0.00388687	intron-variant	MYCBP2	GRCh38.p7	13:77158134	AAAAAAGAATATTTA[C/T]ATATTCTTAAAAATA	23077
rs745903802	snp	A/G	3.43295e-05	0.00414289	intron-variant	MYCBP2	GRCh38.p7	13:77218009	CAAAACTCAACTAAA[A/G]TAAAAACAATAAGTA	23077
rs745905636	snp	C/G/T	3.30492e-05	0.00406494	intron-variant	MYCBP2	GRCh38.p7	13:77194280	ATCATTTATATAAAT[C/G/T]AGCTATACATATCTG	23077
rs745908738	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77167353	GAACATCTTATCCTA[C/T]CAGAAAGCAAGGAAG	23077
rs745920549	in-del	-/ACGTGTGTGCGTGCGCATGCACAC			intron-variant	MYCBP2	GRCh38.p7	13:77310768	CACACAGAGACACAG[-/ACGTGTGTGCGTGCGCATGCACAC]ACACACACACACCAT	23077
rs745933842	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77279950	GAACATGTCTTAAAC[A/G]GCTTGTATTATCTTC	23077
rs745943327	snp	C/T	1.65244e-05	0.00287436	missense	MYCBP2	GRCh38.p7	13:77061186	GTGTGTTCTCGGAAT[C/T]CCACCATTGCCTTCA	23077
rs745946179	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77277016	ATATGCCAAAGCCAG[C/T]ATTAAGAACAAGTTC	23077
rs745952498	snp	A/G	4.06042e-05	0.0045056	intron-variant	MYCBP2	GRCh38.p7	13:77181951	AAATATGGCCCCCCA[A/G]CCAAAAAATATAGCA	23077
rs745956347	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77211600	TGGTCTTCGTGAAAT[G/T]TCAAAGTTGGATTTA	23077
rs745963347	snp	A/G	0.00014846	0.0086144	synonymous-codon	MYCBP2	GRCh38.p7	13:77205352	TATAGCTTCTACTGA[A/G]TGGGCAGAATAACCC	23077
rs745978933	snp	A/C/T			intron-variant	MYCBP2	GRCh38.p7	13:77070892	TTGAAATAAAAAGAA[A/C/T]AAAATCTCAGAACTT	23077
rs745985173	in-del	-/AACATAACATAACAT			intron-variant	MYCBP2	GRCh38.p7	13:77317939	AAGACTCCGTCTCAA[-/AACATAACATAACAT]AACATAACATAACAT	23077
rs745994650	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77310261	ATTTTTATGCACCCC[A/G]CTACCTACATTGTAG	23077
rs745996063	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77154767	ATCAAAAATCTGTCC[C/T]TGAGTAGTAATTTTT	23077
rs745996128	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77282994	CTGCCTAAATGGTTC[C/T]TCTGTCTCCAGTCTC	23077
rs746003600	in-del	-/CAGTAATATCACTTCTATTTAAACAGAAATGATAATATATTTTTACTA	1.6552e-05	0.00287676	cds-indel	MYCBP2	GRCh38.p7	13:77270055	GATGTAGAATTGTAT[lengthTooLong]ATATGGCCCTGCAAA	23077
rs746005238	snp	A/G	1.95593e-05	0.00312718	intron-variant	MYCBP2	GRCh38.p7	13:77261403	AAAAAAAAAGGAATT[A/G]TGGTACTTTTTGGAA	23077
rs746019680	in-del	-/AT			intron-variant	MYCBP2	GRCh38.p7	13:77048918	TTTCTGTTTTTTAAC[-/AT]AGAGGAAACTTTAAG	23077
rs746034526	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77184335	CTGTAATTCTACTGT[A/G]GTCTGAAAATATATT	23077
rs746035395	snp	C/T	1.6473e-05	0.00286988	synonymous-codon	MYCBP2	GRCh38.p7	13:77168605	CAAAATGGCAACTGA[C/T]GGAAGCAATTGTTGG	23077
rs746040257	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77289212	TGGAAAAAAAAAATA[C/T]ACTTGTTAAATAAGA	23077
rs746057949	snp	A/G	4.94287e-05	0.00497111	missense	MYCBP2	GRCh38.p7	13:77125459	CCCATGTCCCTTCAG[A/G]ATTGGTTACCTGGTA	23077
rs746063858	in-del	-/AGC			intron-variant	MYCBP2	GRCh38.p7	13:77202045	AATAACTAAAATCAG[-/AGC]AGAACTGAAGGAAAT	23077
rs746069764	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77147982	TGAAATATTGCATTC[C/T]GTTGTGGTAACAAAA	23077
rs746070841	snp	A/T			synonymous-codon	MYCBP2	GRCh38.p7	13:77097581	TTTCTTTTTAAGAAC[A/T]GCACAGGAACCAGGA	23077
rs746080142	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77275746	CCTAGCATTTTGGGA[A/G]GCTGAGGTGGGCAAA	23077
rs746088430	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77234418	TACTGCCCTCTAATA[A/G]AATTTCATAAATGTC	23077
rs746093747	snp	A/G	0.000183284	0.00957124	intron-variant	MYCBP2	GRCh38.p7	13:77118293	TAAGCAACTCAGAAC[A/G]AAGCTTCAGAAATGC	23077
rs746126182	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77307860	GCTTCTAGAACCTCT[A/G]CTTTAGTGTTCCTTC	23077
rs746144525	snp	C/G	1.66674e-05	0.00288676	intron-variant	MYCBP2	GRCh38.p7	13:77068551	AATGGAAAGGCTGTA[C/G]TGTGATCAGTCACCT	23077
rs746151215	snp	A/C/T	3.30023e-05	0.00406205	missense	MYCBP2	GRCh38.p7	13:77098648	GTGGAGAACTAGCAC[A/C/T]CGATGGGCTAGACCT	23077
rs746155785	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77094968	GCTGGTAGGTGCCCA[G/T]TTGGTATTCATTTAA	23077
rs746157210	snp	C/T			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77083713	TTTCATTTCTCATTA[C/T]AACCCTCAGATGGCT	23077
rs746168508	snp	A/G	1.64768e-05	0.00287021	synonymous-codon	MYCBP2	GRCh38.p7	13:77243126	TTGTCGTAACTGAAG[A/G]TGTTCTTCAATGTTA	23077
rs746168802	in-del	-/ACACAA			intron-variant	MYCBP2	GRCh38.p7	13:77245779	CACACACACACACAC[-/ACACAA]AGGAAATAAAAACAT	23077
rs746178022	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77060291	AATATTTACAGAAAA[A/G]TCTATTTAAAAAGGA	23077
rs746182465	snp	C/T	5.63121e-05	0.00530593	intron-variant, missense	MYCBP2	GRCh38.p7	13:77118433	CAGCTTGATCAAAGA[C/T]GGAAGGAGCTGGGAG	23077
rs746191003	in-del	-/TT			intron-variant	MYCBP2	GRCh38.p7	13:77221944	TAAAACATCTCTAGA[-/TT]ACTTATAATACCTAA	23077
rs746195796	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77096188	TGTATATGATTTCCA[C/T]TATAAAAGCTGATCT	23077
rs746202161	snp	A/G	6.33092e-05	0.00562588	intron-variant	MYCBP2	GRCh38.p7	13:77051769	AAAATAATACTATTT[A/G]ACATTTCTAAACTGT	23077
rs746209988	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77287992	ACCTTAGTTATAAAG[C/T]TGCAGAGTTTTCCTT	23077
rs746210833	snp	A/G	1.66112e-05	0.00288189	missense	MYCBP2	GRCh38.p7	13:77089004	GAAAGCTCAGGAGAC[A/G]GATGTCTCAAAAGGG	23077
rs746217586	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77197350	TTTGTGGAGAAGAAA[C/G]AGATATAGGAGGCCT	23077
rs746229311	snp	A/C/G	3.44058e-05	0.00414752	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77078793	ATTTCTCTCTAGGTA[A/C/G]CGAAACATTTAATGA	23077
rs746234072	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77252864	GTACTGAGCACTATT[G/T]GTAACTAGCTCTATA	23077
rs746235767	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77198224	ATGTGCTACAAGAGT[C/T]CTAATCATTATTCTA	23077
rs746249378	snp	A/T	1.65184e-05	0.00287384	missense	MYCBP2	GRCh38.p7	13:77176552	TCACTGGGTGAGTCA[A/T]CCGTTGTGTACGTTC	23077
rs746262065	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77254623	GGATATTCTAAATTC[C/T]CTCTTCTAGCTATTT	23077
rs746262130	in-del	-/AA	0.000477156	0.0154386	intron-variant	MYCBP2	GRCh38.p7	13:77045533	GGAAAATAATGTTTT[-/AA]GAATACACACATATA	23077
rs746268379	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77047653	AGCACAGGGCATTGT[G/T]CCTAAAGACATGCCC	23077
rs746274775	snp	A/T	6.19867e-05	0.00556682	intron-variant	MYCBP2	GRCh38.p7	13:77296705	AAAATGGGAAAAAAA[A/T]ATGAATGTTCATATT	23077
rs746282897	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77224243	AGCTTTTCTCCTGAA[A/G]CTACAAAATCCTTTA	23077
rs746286111	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77298891	ATTGTGAGGGCATGA[C/T]GAATGTCTATTTCAA	23077
rs746287598	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77239178	AACTTAGTTCAGACT[C/T]GGTAAATAAGATGAG	23077
rs746291525	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77146977	CAGTTTATAATAAGC[A/G]TCCATCAATGGGAGA	23077
rs746308214	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77316162	TATGATTATTTACAC[A/C]GAACATCCCAGGGAA	23077
rs746318863	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77158948	AATTTTAGGTTTCAC[C/T]TATCTGACAAGCAAG	23077
rs746323854	snp	C/T	3.29462e-05	0.00405857	intron-variant	MYCBP2	GRCh38.p7	13:77140809	TGACAAACGTAAAAA[C/T]TGAATGATTCCGGCT	23077
rs746334567	snp	C/T	1.65296e-05	0.00287481	missense	MYCBP2	GRCh38.p7	13:77161953	CTTCTTCTAATTCAT[C/T]ACCTGTTGTGTAAAT	23077
rs746339203	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77145663	TAATTATTTTTTCCA[A/G]GTTTCTATTTTAAGT	23077
rs746340453	snp	A/G	1.69689e-05	0.00291275	intron-variant	MYCBP2	GRCh38.p7	13:77061317	CTATTATTTCATTAA[A/G]GAACAGGGAAAAATA	23077
rs746343125	snp	A/T	1.66757e-05	0.00288749	missense	MYCBP2	GRCh38.p7	13:77262073	CATTTGCTGTTTTCA[A/T]TAGCGCAAACTCTCG	23077
rs746350147	in-del	-/GGGG	1.72121e-05	0.00293356	intron-variant	MYCBP2	GRCh38.p7	13:77067878	CCTGGTAAGAAAAAT[-/GGGG]AAAATGAGAGAATTC	23077
rs746352827	snp	C/T	1.67116e-05	0.0028906	intron-variant	MYCBP2	GRCh38.p7	13:77233290	CATTTTGTATGTGCA[C/T]AGAAAAACTCACAAA	23077
rs746378781	snp	A/G	6.63653e-05	0.00576005	intron-variant	MYCBP2	GRCh38.p7	13:77140977	AACTGTAACATTTGA[A/G]AAAAAAAGAGAAGGA	23077
rs746382541	snp	A/C			intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326149	CTACCTCAACGATAC[A/C]CACACGTGTCACAGC	23077
rs746383130	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77267614	AGATTAGGCCATAGA[C/T]GGCCAAGTTTGAAAA	23077
rs746385305	snp	A/C	1.65946e-05	0.00288046	missense	MYCBP2	GRCh38.p7	13:77185134	AGCAGATCACAAAGG[A/C]AAGCCCACTGTAAGG	23077
rs746402675	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77216601	ACTTACAGAGTATCT[G/T]GGCCTGGGTGCACAA	23077
rs746417548	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77059042	CCAGTCACCACTCTC[C/T]GCATCACCAAAATGC	23077
rs746427579	snp	C/T			intron-variant, nc-transcript-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075570	CTGACCACTCCAGGG[C/T]ACAATGATCTCAAGG	23077
rs746428810	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77148480	CTATTCTTATATCTA[C/G]TTTGACGTCTAGTCC	23077
rs746433202	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77303006	TGATAGAACAAGTAG[A/C]GACCAAAACAGCACT	23077
rs746434809	snp	A/G	4.9561e-05	0.00497775	synonymous-codon	MYCBP2	GRCh38.p7	13:77088868	AGCAGATTTCCTTAG[A/G]GCCTGTTTCATTGCT	23077
rs746439469	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77219108	CTCTTTGAGAGAGAA[A/T]AGAAGAGATCCTAAT	23077
rs746446635	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77317323	AAGTATAACAGGATT[C/T]TCATAGCGCCCTCTG	23077
rs746448322	snp	A/T	4.22342e-05	0.00459514	intron-variant	MYCBP2	GRCh38.p7	13:77118313	TTCAGAAATGCTTGA[A/T]GAGGCAGGTAAGGCT	23077
rs746449254	snp	A/C/G	8.98859e-05	0.00670342	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77082040	ATAATTATTTTCCAG[A/C/G]AACATCTAAGGAACT	23077
rs746453267	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77185043	ACTGCAATTTATTTT[C/T]TTGAAGAGTATTAAG	23077
rs746469200	snp	C/T	2.06648e-05	0.00321434	intron-variant	MYCBP2	GRCh38.p7	13:77260397	GTATTGAAACTTCTT[C/T]GCATAAAAGTAAAAC	23077
rs746482435	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77283408	TTATCCCTACAAGAC[A/C]ATGCTTTCTTGAGGG	23077
rs746498302	snp	A/G	6.61573e-05	0.00575102	missense	MYCBP2	GRCh38.p7	13:77156135	TAGGCCAACCACAAC[A/G]AATATCATCCTTATT	23077
rs746499495	snp	C/T	1.6486e-05	0.00287102	synonymous-codon	MYCBP2	GRCh38.p7	13:77058353	TTCGTTTTTAACACC[C/T]CCGCATGGATGGCCA	23077
rs746499645	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77267728	CAAGATTTTTAAAAC[C/G]CTTTTATAAGCAAGC	23077
rs746499953	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77324959	GGCAAACTGTCTCAC[A/G]TAGTTTTGTGCTATT	23077
rs746502230	snp	C/G	2.47583e-05	0.00351831	intron-variant	MYCBP2	GRCh38.p7	13:77126558	CTGAAAATTTGAATA[C/G]GAAAGAAAAATAAAC	23077
rs746513326	snp	A/G			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77077692	AGCAAAATTATATGA[A/G]TGAAATAATTACAAA	23077
rs746518707	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77232664	ACCATCAAATATTTG[C/T]ATATTCATTTGTTGT	23077
rs746521366	snp	C/T	1.65395e-05	0.00287567	missense, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77077372	CCCAGCCAATGTGCC[C/T]GGAATCCAGATCAAC	23077
rs746521464	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77317466	CCACTCCTAATTTCA[C/T]GTGATCTTCCTACTG	23077
rs746523849	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77111963	ACTGACACTAGGTCA[C/G]TTAAAGCTGCACATG	23077
rs746536425	snp	A/G	3.41093e-05	0.00412959	intron-variant	MYCBP2	GRCh38.p7	13:77181665	CCATTTAGAGTTTTA[A/G]TGCCTCTGTATAAAA	23077
rs746543262	snp	C/T	1.6492e-05	0.00287154	missense, splice-donor-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77083114	GCAAGCGGTGAAAGG[C/T]GTGTGGTAAAGGATG	23077
rs746553383	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77060481	CCAACACTGGAAGTT[C/T]GTGTCAGTCAAATGG	23077
rs746562718	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77125792	CCTAACACAGCCGAC[A/T]TGCTATTATTTAGGT	23077
rs746576983	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77261113	CTTAATAAAGTTTTA[C/T]TTTTACTAAAATAAA	23077
rs746588480	snp	C/T	1.65329e-05	0.0028751	intron-variant	MYCBP2	GRCh38.p7	13:77225386	GAAGAAATAAGTTAC[C/T]GAGCACAATTGTAAA	23077
rs746606655	snp	C/T	1.64743e-05	0.00287	synonymous-codon	MYCBP2	GRCh38.p7	13:77150902	CTTTGCTTGATCTTG[C/T]TGTAAAGACATTTTT	23077
rs746606786	snp	C/T	1.64969e-05	0.00287196	synonymous-codon	MYCBP2	GRCh38.p7	13:77166504	CTGTGCAGTACCACA[C/T]TGAGGGTCAAATTCG	23077
rs746608163	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77154337	TAGGAGAAGCAAATA[C/T]ATGGAGGAGAAAGAA	23077
rs746612501	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77296513	ATACTAATAAAATGG[C/T]TTAATTATATTTTTT	23077
rs746614104	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77191008	TTTAGAATACATAAA[C/T]CATAGTAATAGAATA	23077
rs746620155	snp	C/T	1.69146e-05	0.0029081	intron-variant	MYCBP2	GRCh38.p7	13:77058182	TTCCCCATCTTAATG[C/T]CTGGATACATTCAAT	23077
rs746623978	snp	C/T	1.68369e-05	0.0029014	intron-variant	MYCBP2	GRCh38.p7	13:77067540	CTGAACAGTAGCTCA[C/T]TCTATTCTGTTTTGG	23077
rs746627447	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77060768	AAATCATACAACCTT[-/A]ATAATAAATAGAGAT	23077
rs746629971	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77247477	GATTAGAAGACTTAA[C/T]GTTTTTAAGATGTTC	23077
rs746633226	in-del	-/T			intron-variant	MYCBP2	GRCh38.p7	13:77182957	TACTTTCCTGAGAGG[-/T]TTTTCATCATTGAGT	23077
rs746634013	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77139703	TATTACCAGAAAAAT[A/G]TACTGTCCAAAGTTA	23077
rs746650630	snp	C/T	1.72065e-05	0.00293308	intron-variant	MYCBP2	GRCh38.p7	13:77190223	CAAAATAATAAACCA[C/T]ACTAATTCAGTATAA	23077
rs746653673	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77217159	AAGTACACATTTACA[A/G]TTTTTAAAAAATCAA	23077
rs746695422	snp	A/G	3.30726e-05	0.00406635	missense	MYCBP2	GRCh38.p7	13:77095478	TAACACAGAATGCTC[A/G]GTTCTGCTGCACTGC	23077
rs746698512	snp	C/T	3.30415e-05	0.00406444	intron-variant	MYCBP2	GRCh38.p7	13:77269972	AAGAAAATTTTGGTT[C/T]ATTGTGGATAGTTTC	23077
rs746700270	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77141180	GGGGCTCCCTATCTT[C/T]AACTAGAACATATGA	23077
rs746716891	snp	C/T	1.71484e-05	0.00292812	intron-variant	MYCBP2	GRCh38.p7	13:77190377	AAACAACATGATCAT[C/T]ACAGGAAATAAGAAA	23077
rs746720676	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77054031	TACCAAAATCATGTG[A/G]TGGTGGTGTTGATGG	23077
rs746727174	snp	C/T	1.66313e-05	0.00288364	intron-variant	MYCBP2	GRCh38.p7	13:77156049	CTAATTTAATCCAGT[C/T]ATAATTACCTTCATA	23077
rs746727948	in-del	-/G	1.78493e-05	0.00298736	intron-variant	MYCBP2	GRCh38.p7	13:77164576	TGCTGCTTTAAAAAT[-/G]GTTTGAATGATAATA	23077
rs746731047	snp	C/G	1.65299e-05	0.00287483	synonymous-codon	MYCBP2	GRCh38.p7	13:77098397	TACCACATGGGGAGA[C/G]GGAGCTCTATTTTCA	23077
rs746736571	snp	C/G	0.000132133	0.00812706	missense	MYCBP2	GRCh38.p7	13:77097825	ATGCTACCCATCTTA[C/G]ATATATCTGGTCCAT	23077
rs746738817	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77066683	AAAATATAGTTAGAT[A/G]TTATAAACAGATATC	23077
rs746743484	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77281512	CAACACATGCTTTCG[C/T]ACTTCTCTTCAGAAA	23077
rs746746636	snp	A/G	0.000105178	0.00725107	intron-variant	MYCBP2	GRCh38.p7	13:77263644	AACACTTAATTTGCT[A/G]TCTTACTTATAATAT	23077
rs746753851	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77102801	ACTAAAATAGTAAAA[G/T]GATTTTTATATTATA	23077
rs746764214	snp	C/G	1.7959e-05	0.00299652	intron-variant	MYCBP2	GRCh38.p7	13:77205628	AAACAAAATTTAACT[C/G]CTTGAAATTAAAATG	23077
rs746768751	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77259014	ATTCCCAGCACTTGA[A/G]GAGGCTGAGGCGAGT	23077
rs746771679	in-del	-/CACAA			intron-variant	MYCBP2	GRCh38.p7	13:77245780	ACACACACACACACA[-/CACAA]AGGAAATAAAAACAT	23077
rs746784038	snp	C/G	4.95872e-05	0.00497907	intron-variant	MYCBP2	GRCh38.p7	13:77165257	TTAAAAGAATGAAAA[C/G]ATAATTCATTCTTAC	23077
rs746789057	snp	G/T	3.75192e-05	0.00433107	intron-variant	MYCBP2	GRCh38.p7	13:77055514	TCTTAATCATATAGG[G/T]AAGCTCTAGTTTTTA	23077
rs746791559	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77209458	AAACATCAATTTACA[C/T]CTAAGTCCAAACCAG	23077
rs746807911	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77189409	AGTCCAATGCAACAC[A/G]TTATGTTTGTAGAGC	23077
rs746815665	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77053062	AGGCTTGTTTGAGCC[A/C]AGGAGGTGGAGGCTG	23077
rs746824378	snp	C/T	1.65594e-05	0.0028774	missense	MYCBP2	GRCh38.p7	13:77090238	TCTTTGCAAGATCAG[C/T]ATCAGTTATGGGACT	23077
rs746825258	snp	A/G	1.65116e-05	0.00287324	intron-variant	MYCBP2	GRCh38.p7	13:77062708	CAGAGCTGTTGAAAG[A/G]GAAGGCTGTTACACC	23077
rs746828574	snp	A/C	1.65641e-05	0.00287781	missense	MYCBP2	GRCh38.p7	13:77098002	TTTAGGAAAGAAGAA[A/C]AAGCCATTGCATCAT	23077
rs746830963	snp	A/T	1.64727e-05	0.00286986	missense	MYCBP2	GRCh38.p7	13:77185897	TAAATTTCACAGGTA[A/T]AGACACGCAATAACC	23077
rs746837580	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77309175	TACTCCCATGTCCAG[C/T]CTCACTTTCCCACTT	23077
rs746877271	snp	C/T	1.64768e-05	0.00287021	missense	MYCBP2	GRCh38.p7	13:77139270	CAGTGTAACCATTCA[C/T]GTTAGGGACATACTT	23077
rs746888984	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77164234	TCAAAGCATGTATAT[A/G]CATAAAAAGGGTGTC	23077
rs746891164	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77182656	TTGTGCACTAGTCCA[C/G]GCAATAATCTTGCCC	23077
rs746892515	in-del	-/ACT			intron-variant	MYCBP2	GRCh38.p7	13:77256927	CAAAGAGATATCTGC[-/ACT]ACTCTCATGTTTATT	23077
rs746916709	snp	G/T			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77080676	GCTGGGTGCAGTGGC[G/T]CATGTCTGTAATCCT	23077
rs746917243	snp	C/T			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77079592	TCTGTGGTAGGCAGG[C/T]TGAGGAACATGGAGG	23077
rs746919121	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77272377	ATACTCCTGCTATGA[G/T]CTCTAATGGCATTCC	23077
rs746925496	snp	C/T	1.65021e-05	0.00287241	missense, utr-variant-5-prime	MYCBP2	GRCh38.p7	13:77225518	GGGTATGTTGTGATT[C/T]TGCTTGCATCCTTTT	23077
rs746937184	snp	A/G	1.64955e-05	0.00287184	missense	MYCBP2	GRCh38.p7	13:77098813	TACTGTGGGAATCTG[A/G]CCTCAACTTTGCAGC	23077
rs746941527	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77095740	ATAAGATTATAAAAA[A/G]CAACATTCATTTCAT	23077
rs746941901	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77322190	GCTAAAATGACTACT[C/T]AACCTCTTACAACCA	23077
rs746966454	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77131255	GGGTGAGTAGTGCAT[A/G]CCTATACTCGTAGCT	23077
rs746990449	snp	A/G	0.00517468	0.050602	intron-variant	MYCBP2	GRCh38.p7	13:77070721	TGTTGCCTTTACATA[A/G]AAAAAGAAAAAAAAA	23077
rs746994475	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77323288	TGTCATCAAAGTCAC[C/T]GAGTCCATTAGGTTT	23077
rs746999087	in-del	-/TTTTCTAT	1.73069e-05	0.00294162	intron-variant	MYCBP2	GRCh38.p7	13:77146259	TCGTAAAATCATTTA[-/TTTTCTAT]AAAACATTCTCAATT	23077
rs747004492	snp	C/T	1.65067e-05	0.00287282	synonymous-codon	MYCBP2	GRCh38.p7	13:77097737	CATTTCAAAAGTGGT[C/T]TCGGTTTTCCCATCC	23077
rs747005952	snp	C/T	1.65026e-05	0.00287246	missense	MYCBP2	GRCh38.p7	13:77098557	GATTTAGAACGTTCC[C/T]GAGGAGGATCAAGCT	23077
rs747006544	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77065638	AAAAACCATGAGGAC[C/T]GAGGAGAATGAGAAA	23077
rs747009560	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77221690	ACCACCAGCTAAATA[A/G]CAACAACAATAGCCA	23077
rs747011350	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77049644	ATACTCTGTTCTGCA[A/G]TTTGCTTTTTTTTTT	23077
rs747011940	snp	C/T	1.65105e-05	0.00287315	missense	MYCBP2	GRCh38.p7	13:77212130	CATTCCAATATGGCA[C/T]ATCCAAAATTGGTCT	23077
rs747024162	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77108314	GTTAAGGAAAATAAC[A/G]CTTAGGAAAAGCGTA	23077
rs747029643	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77072363	AACATTGTGAATTGA[A/G]TGAAAATAAAAACAG	23077
rs747030944	in-del	-/G	1.70571e-05	0.00292032	intron-variant	MYCBP2	GRCh38.p7	13:77070742	GAAAAAAAAAAAAAA[-/G]AATGAAGTGGTCTCT	23077
rs747035322	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77055834	ACAAACACTTAGCAT[C/G]CACCTAAGTGCCAAG	23077
rs747048988	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77248206	TAGATTGGGAAATAA[C/T]TTCTTGGATATGATA	23077
rs747054783	snp	A/G	1.65004e-05	0.00287227	synonymous-codon, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081574	GTCTGTCAAACTGCC[A/G]ATCATGGCAGGTCGG	23077
rs747056670	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77177505	CGTTGTATTTTTCGT[A/C]GAGATAGGGTTTTGC	23077
rs747060877	snp	C/T	1.86743e-05	0.00305562	intron-variant	MYCBP2	GRCh38.p7	13:77191848	TCAAAAACAATATTT[C/T]CTTACTTCTCTGTCA	23077
rs747074485	snp	C/G	1.64735e-05	0.00286993	missense	MYCBP2	GRCh38.p7	13:77125427	GAACTCTACCATGCT[C/G]TTCTGATCCAGTTGC	23077
rs747080728	snp	A/G	0.000505945	0.0158971	synonymous-codon, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326737	GCCGAGCCCCGAGGA[A/G]GCGGCGGCGGGGGAG	23077
rs747098035	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77252727	TTGGGGTTTTGCCAC[G/T]TCTAATCTATGGGCA	23077
rs747099028	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77194656	TACTAACTGAGATCC[C/T]GGGACCTAGTTTCCT	23077
rs747099380	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77264393	AGTCATTAGTGTCAC[A/G]GAAAAATACGACCTA	23077
rs747114765	snp	A/C/T	4.94176e-05	0.00497059	missense	MYCBP2	GRCh38.p7	13:77168601	GATTCAAAATGGCAA[A/C/T]TGACGGAAGCAATTG	23077
rs747115656	snp	A/G	1.64838e-05	0.00287083	synonymous-codon	MYCBP2	GRCh38.p7	13:77217891	TAAAAGTACTGCCGT[A/G]TGGTTGCTGCCTGCA	23077
rs747116722	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77299640	ACAATATCTGAGGAT[A/G]GGAATATAAAAGAGA	23077
rs747125473	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77057308	ATTAACTAGGCCTTT[A/G]GCTTCTCCTGCTTTT	23077
rs747136636	snp	A/C			intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326335	AAGTGCTCCTGCCAA[A/C]AGACATCCAGAGCGG	23077
rs747154577	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77249097	AACAAGAATAGTGGA[C/T]GCCAGAGGCAGGGGA	23077
rs747179900	in-del	-/C	1.65855e-05	0.00287967	intron-variant	MYCBP2	GRCh38.p7	13:77270076	GCCCTGCAAAAAAAA[-/C]AAAAGTTAGTATATC	23077
rs747186066	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77277209	CATTCCAATTATTTG[C/T]TAACTAACAAACCAA	23077
rs747194205	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77175009	CACCCAGCCTGGAGT[G/T]CAGTGGTGCAATTTT	23077
rs747195842	snp	A/G	3.43631e-05	0.00414492	missense	MYCBP2	GRCh38.p7	13:77186051	GAATACTCAACAATG[A/G]CTCAAAACATTCCTA	23077
rs747202475	snp	A/G	2.47921e-05	0.00352071	intron-variant	MYCBP2	GRCh38.p7	13:77243985	AAAAAAAAAAAAGAC[A/G]ACTGAGATATTCCTA	23077
rs747204310	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77262891	AATTATAAAAATACT[A/G]CATAATTAGAATATA	23077
rs747205701	snp	C/T	1.69023e-05	0.00290704	missense	MYCBP2	GRCh38.p7	13:77055725	CATAGAGTTCTTTTA[C/T]TGGATCAAGTAGGTC	23077
rs747215538	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77135545	TCATACCTGTCCCTG[A/C]CTATGCCAGGCCTCT	23077
rs747233863	snp	A/C	3.33856e-05	0.00408555	intron-variant	MYCBP2	GRCh38.p7	13:77121543	TCTTACGTGCTATTC[A/C]CTATTCATACAACAA	23077
rs747234877	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77226139	TATTCATGTTTCCTG[G/T]GCCACCATCACCTTC	23077
rs747238318	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77120004	TGTCTCAAACATTTA[C/T]ATTTATTTTAATGAT	23077
rs747241608	in-del	-/AA			intron-variant	MYCBP2	GRCh38.p7	13:77166727	AAGGAGGAACAGAGT[-/AA]AGAGGACAGAGATAA	23077
rs747247995	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77283521	AAGAAATGATCCTAG[G/T]TAAGTCTAAATCTTT	23077
rs747254764	snp	G/T	1.97101e-05	0.00313921	intron-variant	MYCBP2	GRCh38.p7	13:77177721	CAACCCACTAATCAG[G/T]ATAAATACTAAAAGG	23077
rs747270690	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77211792	CATTCTTTCAGCATA[C/G]AGACACATATAAACG	23077
rs747286523	snp	A/T	1.64732e-05	0.0028699	missense	MYCBP2	GRCh38.p7	13:77168469	TATACGGGTGCTCAC[A/T]CTCTATGACAGCATA	23077
rs747293759	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77102473	TTTTATTTAAATACA[A/G]GATTTTAAAAGATTT	23077
rs747294141	snp	A/G			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77083958	AACAAACTGATCTGT[A/G]TTCTTTTAACAATAA	23077
rs747295777	snp	G/T	1.65776e-05	0.00287898	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081417	CCGTAAATCACGTTT[G/T]CTTTCTTACCCCAAG	23077
rs747296932	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77071052	AACAATCCAGGAAAA[C/T]AACATTTGTTTAAAA	23077
rs747325187	in-del	-/TC			intron-variant	MYCBP2	GRCh38.p7	13:77159660	GTAGGCCTTTCCCCT[-/TC]TCTCTCTCCTGCTGC	23077
rs747332511	snp	A/C			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228024	GGTCTTAATCTTTAT[A/C]AGCAGCAGTGGCAGA	23077
rs747338506	snp	C/T	1.64822e-05	0.00287068	missense, intron-variant	MYCBP2	GRCh38.p7	13:77233207	GATGGGATCTGAGTC[C/T]GGCTAGAGCCTGTTC	23077
rs747349243	snp	C/T	1.66935e-05	0.00288903	intron-variant	MYCBP2	GRCh38.p7	13:77088805	TGTATAATCAATGAA[C/T]CAGTAATTTCATTAA	23077
rs747352613	snp	C/T	3.58198e-05	0.00423186	intron-variant	MYCBP2	GRCh38.p7	13:77059678	GATGTTTTCTAGATA[C/T]GTTAACAGAACTAAA	23077
rs747354512	snp	A/T	5.12851e-05	0.00506359	intron-variant	MYCBP2	GRCh38.p7	13:77045534	GAAAATAATGTTTTA[A/T]GAATACACACATATA	23077
rs747354860	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77099434	TTTCCAGCAGAGTGA[C/T]ACCTCGCATCCTTAG	23077
rs747370005	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77049213	TCCAAGCATGGCTCA[C/T]ATCTCTGTTCTGTCC	23077
rs747371707	snp	C/T	1.64789e-05	0.0028704	missense, utr-variant-5-prime	MYCBP2	GRCh38.p7	13:77288238	TCTGCACAGAGTTCT[C/T]AGATGCGGCTGCCAA	23077
rs747382207	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77241598	GCAATTTTCCCATAT[A/G]CTTATATAATGTAAA	23077
rs747392656	snp	C/T	1.68559e-05	0.00290304	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77077099	GTTACACTCTTAAAA[C/T]ATATTACATCAATTA	23077
rs747396042	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77240090	AGTATATCATATTCA[C/T]CTAATTTTGTTTTCT	23077
rs747396149	snp	A/G	1.66388e-05	0.00288429	intron-variant	MYCBP2	GRCh38.p7	13:77233281	GAGGAGAAACATTTT[A/G]TATGTGCATAGAAAA	23077
rs747397867	snp	A/T	1.69588e-05	0.00291189	intron-variant, nc-transcript-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087642	TGAAAGCCTGAAGAA[A/T]TGACGGTTAAATGAG	23077
rs747401240	snp	A/C	1.64743e-05	0.00287	missense	MYCBP2	GRCh38.p7	13:77174380	CTCAAGCTGCACGTG[A/C]TGAATGTGAATGTCA	23077
rs747406442	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77161400	AAAGCAAACAATAAT[A/T]AAAACAACAAATGAT	23077
rs747408394	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77303844	AAACCACAAATTAAA[C/T]GCAAAATATGTAGTA	23077
rs747411751	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77134513	AACTCCAGCTTGGGT[A/G]GCAGGGCAAGGTGCT	23077
rs747422444	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77223896	TGCACGATCATGTCA[C/T]GAACTAAAACTAAAA	23077
rs747426330	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77324864	AAATAAATTTAAATT[A/C]TTTGAGAGGAGTTTG	23077
rs747441064	in-del	-/A	3.32513e-05	0.00407732	intron-variant	MYCBP2	GRCh38.p7	13:77095611	TTTGACCTGGCGAAG[-/A]AAAAAAATCAAACTA	23077
rs747444568	snp	A/C	1.64798e-05	0.00287047	missense	MYCBP2	GRCh38.p7	13:77051068	TCATGACAAGCATTA[A/C]AAAAATGTGTTGTTC	23077
rs747446174	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77147064	TGACCTATAGCTACA[C/T]GGCTGAACCTCAAAA	23077
rs747451542	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77117998	CTTAGAAAAAACAAA[C/T]AAACCTGTCCAAACA	23077
rs747456710	snp	C/G	1.69789e-05	0.00291362	intron-variant	MYCBP2	GRCh38.p7	13:77168697	CACGTGAAAGTGGTT[C/G]TAAAATTATGCATTA	23077
rs747460066	snp	G/T	1.64817e-05	0.00287064	synonymous-codon	MYCBP2	GRCh38.p7	13:77157938	TAAAGTACATTTACC[G/T]TGCAAGCCTTCCACC	23077
rs747475364	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77219634	ACTGTAACATGAGGA[A/T]AGAAGCAGAGAAGTG	23077
rs747476881	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77186959	TGGGACTACAAGTGC[A/G]CACCACCATACCCAG	23077
rs747481941	snp	A/G	8.25076e-05	0.00642238	synonymous-codon	MYCBP2	GRCh38.p7	13:77098301	TTCACTGCTGTCATC[A/G]CAGGTGCTGTCTGTT	23077
rs747484711	in-del	-/ACAC			intron-variant	MYCBP2	GRCh38.p7	13:77245852	TATATATATATGTAT[-/ACAC]ACACACACACATATA	23077
rs747493972	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77151250	AAAAGATAGTGGAAT[G/T]AATCTACATTAAGTT	23077
rs747508034	in-del	-/C	2.45927e-05	0.00350653	intron-variant	MYCBP2	GRCh38.p7	13:77055794	ATGAACACTCTTTAG[-/C]CAGAATCATTTATTA	23077
rs747512986	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77062040	TATACTTTGTTACTT[A/G]GAGACTTAAGAAATG	23077
rs747529490	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77112682	GGCCTCAAGCCATCC[C/T]TCTACCTTGGCCTTG	23077
rs747533053	snp	A/G			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77083886	CTGGCAATTTCTATT[A/G]CCAGTTTCTTGGACT	23077
rs747534502	snp	A/G	1.65064e-05	0.00287279	intron-variant	MYCBP2	GRCh38.p7	13:77194257	CAGCTAAGGAAAGGA[A/G]AAAGACAATCATTTA	23077
rs747536620	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77148291	ATTCTTTAACAGCCA[A/G]TGGACAATTCACCTA	23077
rs747539039	snp	A/G	1.82197e-05	0.0030182	intron-variant	MYCBP2	GRCh38.p7	13:77273454	ATAAACTTCTAAGCA[A/G]ATATAAATATGAAAT	23077
rs747573662	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77289596	TAACCACAGCTAACA[A/T]GGTAATAGACTGAAT	23077
rs747579226	snp	C/T	1.64917e-05	0.00287151	synonymous-codon	MYCBP2	GRCh38.p7	13:77261229	TATGCTCCCATCTTC[C/T]GCAACTAAAAGGGCG	23077
rs747582104	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77223803	CCTTTAACAGCAAGA[C/T]TCCAAAGTGGCACCT	23077
rs747584962	snp	C/T	1.6574e-05	0.00287867	missense	MYCBP2	GRCh38.p7	13:77158102	ATTCCAGAATGGGTT[C/T]TGCACACCTGTTAAG	23077
rs747594202	snp	C/T	1.7184e-05	0.00293117	intron-variant	MYCBP2	GRCh38.p7	13:77095309	GATATCAATAAACAA[C/T]CGCTGTTAATCCAAA	23077
rs747594543	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77270714	GAAGCAAATCTCAAG[A/C]AAGGTAGACTTCCTT	23077
rs747595994	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77062246	ATGTTGCCTGTGTTA[C/T]TGCTTTATTTCCTTC	23077
rs747607854	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77305294	CAACAACCCAAATGC[C/T]CACCAACTAATGAAT	23077
rs747617599	snp	A/G	3.30213e-05	0.00406319	synonymous-codon	MYCBP2	GRCh38.p7	13:77211273	CCACTTTATTTATCA[A/G]AAGGCATTTAAATGG	23077
rs747618129	snp	C/T	1.65236e-05	0.00287429	missense	MYCBP2	GRCh38.p7	13:77140120	AGGGAAGGGTGGCTA[C/T]GGATGCGAAGCCCCG	23077
rs747619765	snp	A/G	1.65455e-05	0.00287619	missense	MYCBP2	GRCh38.p7	13:77189045	CCATCACTGGTTGGA[A/G]GTCTAAAGGCAGTAG	23077
rs747629202	in-del	-/TCTA			intron-variant	MYCBP2	GRCh38.p7	13:77050233	TGTTTTCCGGAGAGG[-/TCTA]TCACTTGCACTCTGA	23077
rs747640516	snp	C/T	4.94907e-05	0.00497422	synonymous-codon	MYCBP2	GRCh38.p7	13:77267872	ACCATCTTGCTCCAG[C/T]GTTTCAGGGCTTATC	23077
rs747644462	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77112969	TACTCATTGTCTCCA[A/G]TTTCTCCTTCCCCGT	23077
rs747647344	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77219769	GAGAGTTTGAAGATT[C/T]GAGAAAAGGTGTGGT	23077
rs747661158	snp	A/G	3.29473e-05	0.00405864	missense	MYCBP2	GRCh38.p7	13:77150882	CCAGGAATCCTTTGA[A/G]GTTTCTTTGCTTGAT	23077
rs747679266	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77177148	GAAAAATGACAATAT[-/A]AAAAAAAAAAAAAAA	23077
rs747680162	snp	A/G	1.65452e-05	0.00287616	missense	MYCBP2	GRCh38.p7	13:77095445	GGCAACTGAGATTGG[A/G]ATGGCTTTGCAGGAT	23077
rs747684058	snp	C/T	9.92047e-05	0.0070422	intron-variant	MYCBP2	GRCh38.p7	13:77269956	ACATGTTGTAAAAGA[C/T]AAGAAAATTTTGGTT	23077
rs747690420	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77305398	TACAACATGGATGAA[A/C]CTTGAAAACATTATG	23077
rs747692117	snp	C/T	1.6501e-05	0.00287232	intron-variant	MYCBP2	GRCh38.p7	13:77166285	CTAAATATACATAAA[C/T]GCACTTATTTTACCA	23077
rs747700717	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77240277	TAAAAAATGAATACA[A/T]AGTTAGAATTCTTGT	23077
rs747711867	snp	C/T	1.69089e-05	0.0029076	missense	MYCBP2	GRCh38.p7	13:77257673	ATTAAAGACCTACCT[C/T]TCCCACCTTGGTTCA	23077
rs747714740	snp	A/G	3.30256e-05	0.00406346	intron-variant	MYCBP2	GRCh38.p7	13:77064752	ATTGAGCAGAACAGA[A/G]TATTTTAATAAGTGA	23077
rs747721904	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77049533	TAATCAATAGTATTA[A/G]TTTCTTGAGTATCTT	23077
rs747736912	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77091906	CTTGTCAGACTAGCC[C/T]CAAAACAGTTTCTAA	23077
rs747736967	in-del	-/AACT			intron-variant	MYCBP2	GRCh38.p7	13:77213021	GAAAACACAGCCACA[-/AACT]AACTGTGGAAGCAAC	23077
rs747746699	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77283624	ATTATGCACCAGGCA[C/T]GGTGACTCCTGCCTG	23077
rs747753685	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77126212	GATAAAATACATTAA[C/T]ATTGAAAAACCTGTG	23077
rs747754359	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77148651	CCAAATGATTGTTTT[A/C]TCCATGCTCATATGA	23077
rs747773303	snp	A/T			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076089	CAAAAGTTTTAGGTA[A/T]AGTGTTTTAGTCAGG	23077
rs747823116	in-del	-/T			intron-variant	MYCBP2	GRCh38.p7	13:77286399	GGCACCATTTAAAAA[-/T]GTCTATATTTTCACC	23077
rs747838902	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77219121	AAAAGAAGAGATCCT[A/C]ATTTCCCTTATGAGT	23077
rs747857075	snp	C/G	1.64933e-05	0.00287165	missense	MYCBP2	GRCh38.p7	13:77098176	CTGGTGTGTCTATTA[C/G]CACATTTTCGACTTA	23077
rs747868887	snp	A/G	1.65883e-05	0.00287991	missense, utr-variant-5-prime	MYCBP2	GRCh38.p7	13:77288357	TCTGGTATGATTACT[A/G]TATTCTCTAAGTTTT	23077
rs747876725	in-del	-/G			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77079892	GGAAGCCTGTTAAAA[-/G]GAAAGTAGATGTCAG	23077
rs747877378	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77234633	CTCAATAATGCAGTA[C/T]CAATTATTTTCTCAG	23077
rs747880201	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77211541	TATACCACTCTATTA[C/T]ATAATTATTCACAGT	23077
rs747880386	snp	A/C	1.64882e-05	0.00287121	intron-variant	MYCBP2	GRCh38.p7	13:77070594	CACACACACACACAC[A/C]AAACTAATGAAGACA	23077
rs747885853	snp	A/G	1.69444e-05	0.00291066	intron-variant	MYCBP2	GRCh38.p7	13:77224569	TTATTTTTTCATTAT[A/G]TGCATTTTACATTTC	23077
rs747889087	snp	A/G	3.47754e-05	0.00416971	missense, utr-variant-5-prime	MYCBP2	GRCh38.p7	13:77273647	CGAACGGTGATTTCC[A/G]AAAGAAGCTGGAAGA	23077
rs747889616	snp	A/G	1.64953e-05	0.00287182	missense	MYCBP2	GRCh38.p7	13:77166415	AGATTTTCATGAACA[A/G]ATGTCAATTTTGGTC	23077
rs747900586	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77102815	ATGATTTTTATATTA[C/T]ATAACAATAAGTTTA	23077
rs747910507	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77281836	TTGGATTTAATAATT[A/C]ATTCTTTACCCTTAA	23077
rs747919207	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77232997	CATGACAGTCACTGA[C/T]AAACGGTATCACTTT	23077
rs747940364	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77054258	TGGGTGAGCAGACAG[A/G]GCTGAGTTTGGGAAA	23077
rs747946137	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77141517	GGTTCACAATTGTAA[A/T]CCCAGCACTTTGGGA	23077
rs747960749	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77192592	AAAATCTGTAGAGGT[A/T]TGGAAGTACAAAAGA	23077
rs747960987	snp	A/T	1.73261e-05	0.00294325	intron-variant	MYCBP2	GRCh38.p7	13:77061343	AAATATGCTTATTTA[A/T]CACTCTGAAAGGGAG	23077
rs747979368	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77178960	AAAAAGTTAAAAAAT[G/T]TCTGACAAGGGCTTC	23077
rs747979747	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77070718	TGATGTTGCCTTTAC[A/T]TAGAAAAAGAAAAAA	23077
rs747979769	snp	C/T	1.66125e-05	0.00288201	missense	MYCBP2	GRCh38.p7	13:77205496	CTGTTTACCACACTA[C/T]AATCTTCTTTAGAAT	23077
rs747981592	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77212723	CAGCACAATCAATGG[C/T]AAGATATGATATTTT	23077
rs747986880	snp	C/T	1.68354e-05	0.00290128	intron-variant	MYCBP2	GRCh38.p7	13:77156022	TCATTGCAGCCAGTA[C/T]ATAGATGTCTGCTAA	23077
rs747987190	snp	A/G	1.64746e-05	0.00287002	missense	MYCBP2	GRCh38.p7	13:77058324	CAGCCGTGTAGACAG[A/G]GCAGACAGTGCTCTT	23077
rs747995110	in-del	-/T			intron-variant	MYCBP2	GRCh38.p7	13:77311566	AGAAGTTTTTTTTTG[-/T]TTTTTTTTTTTTGTT	23077
rs748008745	snp	A/G	1.64749e-05	0.00287005	synonymous-codon	MYCBP2	GRCh38.p7	13:77171516	CAAGAGCTCTGTGCA[A/G]GAGGTCCTTAGAGGC	23077
rs748019628	in-del	-/AAGT			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77078326	AAGTTTCATGAATAC[-/AAGT]AAGGGAGCTTGAGCA	23077
rs748020198	snp	G/T	1.99376e-05	0.00315728	intron-variant	MYCBP2	GRCh38.p7	13:77278729	ATATTCACTTTTAAA[G/T]GCTTCACTGAATGAG	23077
rs748022619	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77247737	ACCAATGGGATAGAA[C/T]AGACAGCTGAGAAAT	23077
rs748034101	snp	A/G	1.64808e-05	0.00287057	synonymous-codon	MYCBP2	GRCh38.p7	13:77180286	CTCCAGAACTTCACG[A/G]AAGCTTGTCATCCCT	23077
rs748043822	snp	G/T	1.84606e-05	0.00303808	intron-variant	MYCBP2	GRCh38.p7	13:77257869	AAAAACAACAAAAAG[G/T]CCCTTCTGAGCCTAG	23077
rs748043982	snp	A/G	1.65562e-05	0.00287712	intron-variant	MYCBP2	GRCh38.p7	13:77224447	ATGAAAAGTTAGCAA[A/G]TACCTGGAGTTGACA	23077
rs748047602	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77130833	ATTCTAGTATTAAAG[G/T]AACATGAAAGGCAAT	23077
rs748049098	snp	C/T	1.64917e-05	0.00287151	synonymous-codon, intron-variant	MYCBP2	GRCh38.p7	13:77126426	TCCCGTCTTCACTAC[C/T]TTGTACATGCCTGGC	23077
rs748049194	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77309212	GCCTCCTGAAAAAAG[A/G]AGGTGAAGTGAGTGG	23077
rs748055019	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77275634	TTGAGGCTACCCTGG[A/G]CAATATAGTAAGATC	23077
rs748057013	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77259227	CTGAGATTGTGCCAC[G/T]GCACTCCAGCCTGGG	23077
rs748062690	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77260666	TTTGTATATAAAGCT[-/A]AAAAAAAAAACCCAT	23077
rs748063480	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77167071	TCTGATATTCCCAGT[A/G]TCACTAATAGGAATT	23077
rs748069525	in-del	-/AAAAC	2.17143e-05	0.00329495	intron-variant	MYCBP2	GRCh38.p7	13:77166304	CTTATTTTACCACAT[-/AAAAC]AGAAGAAAAAAAAAA	23077
rs748078241	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77052872	GGTGGCTCACACCTG[G/T]AATCCCAGCACTTTG	23077
rs748093676	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77117973	ATACATTTCATAGAT[A/G]CCAAATTCACTTAGA	23077
rs748096316	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77310055	AGGCGGAGGTTGCAG[C/T]AAGCCAAGATCGCCC	23077
rs748104594	in-del	-/CG			intron-variant	MYCBP2	GRCh38.p7	13:77145223	CACCAATGACCACCA[-/CG]TCCCCAAGTTCAATG	23077
rs748117875	in-del	-/T	1.65364e-05	0.0028754	intron-variant	MYCBP2	GRCh38.p7	13:77140966	AAAATCAGAGAACTG[-/T]TAACATTTGAGAAAA	23077
rs748127956	snp	C/T	1.65817e-05	0.00287933	missense	MYCBP2	GRCh38.p7	13:77121378	AAATACCTACCTTTG[C/T]TATTTCCGAGTCCAT	23077
rs748128884	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77104603	GATGAGGATGTAGAA[A/G]GGAGACTAGAATTCA	23077
rs748132008	snp	A/T	1.68343e-05	0.00290118	missense	MYCBP2	GRCh38.p7	13:77243827	GAAGATCTAAAGGTA[A/T]CATTTCTTTCACTGC	23077
rs748132583	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77053359	AGGAACTGGGACAAT[C/T]TGCATGCACTGATTG	23077
rs748136361	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77094851	TAGCACTCCTCACAT[A/G]GCATTTCAAATGTTT	23077
rs748137857	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77296747	AGCTATCAAAAATGG[G/T]TATTTCCAAAGTAGA	23077
rs748154888	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77196049	AGTAAGTCTATGGTT[A/G]GGAATTGAATTTACA	23077
rs748159691	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77068931	AGACAAGAATGTAAA[C/T]TGATACTCAATTTAA	23077
rs748169962	snp	C/T	1.70793e-05	0.00292222	intron-variant	MYCBP2	GRCh38.p7	13:77181660	TAAAACCATTTAGAG[C/T]TTTAGTGCCTCTGTA	23077
rs748173064	snp	C/T	3.30349e-05	0.00406403	synonymous-codon	MYCBP2	GRCh38.p7	13:77090170	AGGTAAAATGGAGTG[C/T]TGTTTATCATATTCG	23077
rs748174579	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77256117	AAAGGATATTGTGAA[A/G]AAGGTGTGTCTACAA	23077
rs748175724	snp	A/G	1.66225e-05	0.00288287	intron-variant	MYCBP2	GRCh38.p7	13:77263818	AACATCCACAGCATT[A/G]CATTACATAAAGAGG	23077
rs748203074	snp	C/T	6.64419e-05	0.00576338	intron-variant	MYCBP2	GRCh38.p7	13:77146144	GTTTTGGTTATACTT[C/T]GAGAAAACGATCCTT	23077
rs748210555	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77286367	TAGAAAAAAGCAATA[C/T]GCATAAGTCATATAA	23077
rs748211134	snp	C/T			downstream-variant-500B	MYCBP2	GRCh38.p7	13:77044277	CTGAGGCTGGAGGAT[C/T]GCTTGAGCCCAGTTG	23077
rs748224931	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77302283	CTAAAAGCAAAGCAT[A/G]AAGAGAAAATCTTTA	23077
rs748227894	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77046077	AAAACATGAACAATG[G/T]TATAAAATACAATGT	23077
rs748228439	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77130135	TTAAAATCTTTCTAG[G/T]GAGTAGCAATTGCAC	23077
rs748233795	snp	A/C	1.65015e-05	0.00287237	synonymous-codon	MYCBP2	GRCh38.p7	13:77212002	TGTAGCAAGTACATG[A/C]GAATTAATAAGTGCT	23077
rs748261337	snp	A/G			intron-variant, synonymous-codon	MYCBP2	GRCh38.p7	13:77103243	AGATGAGAGAGCAGA[A/G]GCAGGCCCAGCTACA	23077
rs748263435	snp	C/T	8.17544e-05	0.00639301	intron-variant	MYCBP2	GRCh38.p7	13:77177706	GTAAATCCTGATACA[C/T]AACCCACTAATCAGG	23077
rs748263876	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77119816	TACATCCTTAAACTC[C/T]TGGCCTCAAGTGATC	23077
rs748273079	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77070995	ATCTATTTCTAAATT[A/G]TAAACATTATTAGTT	23077
rs748282499	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77238100	TACAAAAAATTAGCC[C/T]GGTGTGGTGGTGAAC	23077
rs748289401	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77149713	ACCTGCCCCTCTTCC[A/T]TTATCAATTGGACAC	23077
rs748290200	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77145112	TCTTCTCCGATTTAT[A/G]TCAAACTCCATTCTC	23077
rs748291796	snp	C/T	3.58333e-05	0.00423265	intron-variant	MYCBP2	GRCh38.p7	13:77263639	GGGAAAACACTTAAT[C/T]TGCTATCTTACTTAT	23077
rs748294854	snp	A/C	3.91137e-05	0.00442214	synonymous-codon, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326563	GCGGTCGGCCAGGGC[A/C]CGGCCTGACAGCAGC	23077
rs748301649	snp	A/T	1.78093e-05	0.00298401	intron-variant	MYCBP2	GRCh38.p7	13:77205622	ACAAAGAAACAAAAT[A/T]TAACTCCTTGAAATT	23077
rs748308347	snp	C/T	0.000133089	0.00815641	missense	MYCBP2	GRCh38.p7	13:77055704	AGGCTTTTCTTCTGA[C/T]ATCCTCATAGAGTTC	23077
rs748312375	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77299807	AAAATAACTTCATAT[C/T]CATCAGATTTGAAAG	23077
rs748330803	snp	C/T	1.66518e-05	0.00288542	intron-variant	MYCBP2	GRCh38.p7	13:77061808	AAAATAAGACATTTC[C/T]ACGTTACTTAGATTA	23077
rs748331939	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77264489	TCAAAACCAGTTGTA[C/T]ATTTCCCACTTAAAA	23077
rs748355178	snp	A/C	3.55051e-05	0.00421323	missense	MYCBP2	GRCh38.p7	13:77185876	TGCATCATACCTGAC[A/C]CTGGGTAAATTTCAC	23077
rs748358629	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77123124	TCATATAAATTACCA[C/T]AGTGCCAAATCTTTG	23077
rs748371480	snp	C/T	3.30229e-05	0.0040633	missense	MYCBP2	GRCh38.p7	13:77097813	TTGTTTTTGTTGATG[C/T]TACCCATCTTAGATA	23077
rs748381139	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77265792	TCTTCAGGCTTGAGG[A/G]AGGAGTCTTCTGCCA	23077
rs748384912	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77253936	TTTTCCAGGAAACAT[G/T]TATAAAGGAGGTTTT	23077
rs748388470	snp	C/T	1.67416e-05	0.00289318	synonymous-codon	MYCBP2	GRCh38.p7	13:77185358	TTTGCTAGTTTCTTC[C/T]ACAACTGCTTTTCCT	23077
rs748422242	in-del	-/G			intron-variant	MYCBP2	GRCh38.p7	13:77180686	TTGGGAGGCTGAGAT[-/G]GGAGGATCACTTGAG	23077
rs748422990	snp	A/G	1.656e-05	0.00287745	synonymous-codon	MYCBP2	GRCh38.p7	13:77176599	AGATGTCCATCTGTG[A/G]GAATGAGTTGAATCT	23077
rs748429579	in-del	-/TTC	1.74424e-05	0.00295312	cds-indel	MYCBP2	GRCh38.p7	13:77097515	CCTAACTTCTGCCTT[-/TTC]TTTTTTCTTTTTTTC	23077
rs748432429	snp	A/G	1.65499e-05	0.00287657	intron-variant	MYCBP2	GRCh38.p7	13:77157900	TGAAGAAAGATGAAA[A/G]CCCTAAAATAAAGTA	23077
rs748437114	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77300910	GCTTGTTCTTCCATG[C/G]GGGTAACTGCAGAGC	23077
rs748443727	in-del	-/AA			intron-variant	MYCBP2	GRCh38.p7	13:77115845	ATTCAAACTACTGTT[-/AA]ACATTAAAAAAAGTC	23077
rs748459817	snp	A/G	1.64882e-05	0.00287121	synonymous-codon	MYCBP2	GRCh38.p7	13:77096345	CTGTTTTTCGCGGAG[A/G]TATTTTTCTCTACAG	23077
rs748460042	in-del	-/TTTTTTTTTTT			intron-variant	MYCBP2	GRCh38.p7	13:77177336	TTTCTTTTCTTTCTT[-/TTTTTTTTTTT]TTTTTTTTTTTTTTT	23077
rs748468000	snp	G/T	1.69436e-05	0.00291058	intron-variant	MYCBP2	GRCh38.p7	13:77260613	AAAAAGAAATTAGAT[G/T]AAATCAAGACCTCTA	23077
rs748470760	snp	G/T	3.59447e-05	0.00423923	intron-variant	MYCBP2	GRCh38.p7	13:77191828	TCTGAGAAAAAATTA[G/T]TGAGTCAAAAACAAT	23077
rs748473642	snp	C/T	1.65869e-05	0.00287979	missense	MYCBP2	GRCh38.p7	13:77181811	GTAATACTTCTCCAT[C/T]ATACGCAATCGGGAA	23077
rs748489444	snp	A/C	1.68125e-05	0.00289931	intron-variant	MYCBP2	GRCh38.p7	13:77068528	ACAATGTTTCAAGTA[A/C]CAAAAGCAATGGAAA	23077
rs748515333	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77187818	TTGGGAGGCCGAGGC[A/G]GGTGGGTCATGAGGT	23077
rs748515468	snp	C/T	4.95774e-05	0.00497858	intron-variant	MYCBP2	GRCh38.p7	13:77139340	ATCATTATGGATCTA[C/T]AGAAAAAAGCAACAG	23077
rs748524324	snp	A/G	6.59294e-05	0.00574111	synonymous-codon	MYCBP2	GRCh38.p7	13:77194224	TTCATGATCTCCTCC[A/G]TCAGGACCCAATTCA	23077
rs748526632	snp	C/T	1.64798e-05	0.00287047	intron-variant	MYCBP2	GRCh38.p7	13:77059516	GCCTGTGTCACTATA[C/T]ACTCACCTGGCAATC	23077
rs748538658	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77149977	ACAAAACACAAATCT[A/C]ATCAAGCCATTCCTC	23077
rs748545731	snp	A/G	1.793e-05	0.00299411	intron-variant	MYCBP2	GRCh38.p7	13:77097319	CAAATAAAGTGATCT[A/G]GTTCATTAAAGAAAA	23077
rs748548983	snp	C/G			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291195	GCAATTCAATAAGAA[C/G]AAGACAATTACAAAA	23077
rs748552861	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77137691	CCTCCTGAGTTCCAG[C/T]GATTCTCCCGCTTCA	23077
rs748554840	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77121742	TCTTATGAAGCCAAT[C/T]TACTTTTATTGTGGC	23077
rs748555925	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77139693	TACTTGGTTATATTA[A/C]CAGAAAAATATACTG	23077
rs748557076	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77187306	TCAACTTAAGACTAA[C/T]AGGATGCAAAGTTAC	23077
rs748564479	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77072474	AGGTCTTGGAGTCTA[C/T]GATCTGATCTTGGAC	23077
rs748568394	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77313001	ACAATCACCAAGACA[A/G]AACATATCCTGGGCA	23077
rs748578921	snp	A/C			missense	MYCBP2	GRCh38.p7	13:77169712	GTTCTGGAATGTCAT[A/C]AGCTAAAAAAAGGCA	23077
rs748586898	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77244937	AACCACCCCATCAAA[A/G]AGTGGGCGAAGGATA	23077
rs748589746	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77134792	AAACAGTTAAAGTCA[C/T]TTTGAACTAAATTAG	23077
rs748592779	snp	A/G	1.64939e-05	0.0028717	missense	MYCBP2	GRCh38.p7	13:77261215	GATCCTGTAAAGAAT[A/G]TGCTCCCATCTTCTG	23077
rs748599315	in-del	-/C	0.000978343	0.0220956	intron-variant	MYCBP2	GRCh38.p7	13:77243965	TCCTAGGGGGAAATA[-/C]AAAAAAAAAAAAAAA	23077
rs748602769	snp	A/T	1.64773e-05	0.00287026	missense	MYCBP2	GRCh38.p7	13:77168445	TGTAATGCATCACAC[A/T]GGCAGGTTTATACGG	23077
rs748603345	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77171223	CTAAAAGAAGAATAA[A/C]GACCCAGTTTAACTC	23077
rs748604334	in-del	-/AGG	0.000247408	0.0111195	intron-variant	MYCBP2	GRCh38.p7	13:77233132	GAAAGTATCCCACCT[-/AGG]AGGTGATAAGGAAGA	23077
rs748604658	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77306407	ATTTTAACAGTTCAA[C/T]TTGATTTAGGGGAGA	23077
rs748607735	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77207287	CATAGAAAGGAAGCA[C/T]AGATAGAATGGATGT	23077
rs748613797	snp	A/G	1.64727e-05	0.00286986	synonymous-codon	MYCBP2	GRCh38.p7	13:77067685	TTTTAGCTGTACAGT[A/G]AGTGCTTTGGCAATG	23077
rs748622594	snp	G/T	0.000512689	0.0160026	missense, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326706	AGAAGGTGGCGGCTG[G/T]GTAGAATCCGTCCCC	23077
rs748647530	in-del	-/ACACACACAC			intron-variant	MYCBP2	GRCh38.p7	13:77166977	ACAAAACACACACAT[-/ACACACACAC]ACACACACACACACA	23077
rs748664401	snp	A/T	1.64909e-05	0.00287144	missense	MYCBP2	GRCh38.p7	13:77212118	GAGCTGGCTTTGCAT[A/T]CCAATATGGCACATC	23077
rs748673573	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77277332	ATGATCACTGGTGCT[A/G]TCATAACAATAACCA	23077
rs748686015	in-del	-/G			intron-variant	MYCBP2	GRCh38.p7	13:77163868	ATCCCAGGAGCATCC[-/G]CCTCTCCTGGTTTCT	23077
rs748686467	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77241861	GCTAGAAAAAAATAT[A/C]ATGATGGTTAAATGG	23077
rs748687890	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77101760	CGTATTTTATATATT[-/A]AAAAAAAACTATGCT	23077
rs748691621	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77056009	TTTATTAGCTTTATA[G/T]TTCCTGCGTCTGAAA	23077
rs748692205	in-del	-/GAG			intron-variant	MYCBP2	GRCh38.p7	13:77246598	AAGGAGAAGGAGGAA[-/GAG]GAGGAGGAGGAGAAG	23077
rs748707778	snp	C/T	3.33762e-05	0.00408497	synonymous-codon	MYCBP2	GRCh38.p7	13:77270332	AGAGCCTATTTTATA[C/T]AATCCATCCTTGCAT	23077
rs748721419	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77100619	ATAGAGTATGGCAAG[G/T]ACTTTATACAGGGCA	23077
rs748722556	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77090879	GCTTTTCTATTTATT[A/T]AAGCAACATTTAAAA	23077
rs748726026	snp	C/T			upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77327121	AGAGCATGCGCCACT[C/T]CTCGCACATGCTCAG	23077
rs748738464	snp	C/T	1.64966e-05	0.00287194	synonymous-codon, utr-variant-5-prime	MYCBP2	GRCh38.p7	13:77288200	TTTGGATTCCTCTTC[C/T]TCATCACTATCTGAT	23077
rs748739468	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77257270	TGGGTGGGAAATGGG[A/G]TGGTTAGTTGGCACA	23077
rs748749638	snp	C/T	1.77934e-05	0.00298268	intron-variant	MYCBP2	GRCh38.p7	13:77211124	CCATAAGAGTATAAC[C/T]GCATCAAAACTTATT	23077
rs748750243	snp	G/T	4.95005e-05	0.00497471	synonymous-codon	MYCBP2	GRCh38.p7	13:77098529	GGTATCTGGATCAAG[G/T]GTGTAAGAGTCTGAT	23077
rs748755954	snp	A/G	1.65803e-05	0.00287922	intron-variant	MYCBP2	GRCh38.p7	13:77233274	GGGGCCTGAGGAGAA[A/G]CATTTTGTATGTGCA	23077
rs748772606	snp	A/C			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77293271	GTCTGAAATAATCAC[A/C]GAAGAAAAGAGAACT	23077
rs748781560	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77050537	TAATTTCTCCTGTAT[G/T]CTGAGTGGTTTCTTT	23077
rs748782328	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77134503	CGTGCCACTGAACTC[C/T]AGCTTGGGTGGCAGG	23077
rs748791591	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77101072	TGAGTATGTGATGTT[G/T]GGAATACTTGTTTTT	23077
rs748792745	in-del	-/GAA			intron-variant	MYCBP2	GRCh38.p7	13:77055146	TTAAAAAAAAAAAAA[-/GAA]GAAGTAGTTAAAGAT	23077
rs748793341	snp	C/T	1.65269e-05	0.00287457	synonymous-codon	MYCBP2	GRCh38.p7	13:77206756	GGACTGCATGTCTGC[C/T]GCAGAGGGAAGCCTG	23077
rs748794302	snp	A/G	4.94328e-05	0.00497131	missense	MYCBP2	GRCh38.p7	13:77243149	CAATGTTAACCCCGG[A/G]CACTGGGACAGCTAG	23077
rs748796021	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77246672	GGGGCAGGGGGAGGC[-/A]AAAAAAAAAAACCCC	23077
rs748810409	in-del	-/CC			intron-variant	MYCBP2	GRCh38.p7	13:77223910	CGAACTAAAACTAAA[-/CC]ACTAAAACAAATGAA	23077
rs748820104	snp	A/C	1.66167e-05	0.00288237	intron-variant, nc-transcript-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076895	AATGACAGGCATTAA[A/C]ACTATATTGGCCAGA	23077
rs748828822	snp	A/G/T	6.59961e-05	0.00574407	synonymous-codon	MYCBP2	GRCh38.p7	13:77098157	CGATTTTTCTTTTTT[A/G/T]GGCCTGGTGTGTCTA	23077
rs748831390	snp	A/C	1.64798e-05	0.00287047	synonymous-codon	MYCBP2	GRCh38.p7	13:77045465	ATGGAGTGGACATTC[A/C]GTTCCTTCTAACTGC	23077
rs748844627	snp	A/G	4.1215e-05	0.00453936	intron-variant	MYCBP2	GRCh38.p7	13:77186107	CAATTAATTCAAATG[A/G]TACCATAAACGGAAT	23077
rs748859335	snp	C/G/T	6.61042e-05	0.00574879	missense, utr-variant-5-prime	MYCBP2	GRCh38.p7	13:77288349	GTTTGATATCTGGTA[C/G/T]GATTACTGTATTCTC	23077
rs748861514	snp	A/T	1.71405e-05	0.00292745	missense	MYCBP2	GRCh38.p7	13:77264002	CCTTCAGTGTGGCAA[A/T]CTGTGCAAAAGAAAA	23077
rs748864424	in-del	-/TTTA	0.000134828	0.00820949	intron-variant	MYCBP2	GRCh38.p7	13:77180353	GTTCTAAGGTATTGT[-/TTTA]TTTTCCTTCATAGGA	23077
rs748886824	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77305535	AAAACTGATAGAAAG[C/G]AGAATAGAAACTGAC	23077
rs748888515	snp	C/T	8.88881e-05	0.00666604	intron-variant	MYCBP2	GRCh38.p7	13:77171683	ATGGTAAGTAAAACA[C/T]GATCCAGTGCCAGAA	23077
rs748895492	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77174935	ATATATATATAATAT[-/A]ATATATATTTTATAT	23077
rs748898205	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77270937	TTTCTTCCTCTTTAT[C/G]TTTCAGTTCACCATT	23077
rs748907795	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77320117	TCTTATAGCAAAAGC[A/G]CTAGGCATTTATATC	23077
rs748908622	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77099944	TTAGAGCCAGGCTGT[A/C]TGTGACCCAAGTAAA	23077
rs748929475	snp	A/G	1.66112e-05	0.00288189	missense, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076756	AAATAAATACATTGT[A/G]TACTTTTTCTTCTCC	23077
rs748932979	snp	C/T	1.66871e-05	0.00288847	missense	MYCBP2	GRCh38.p7	13:77181885	ACAGCTGCAAGGAGT[C/T]GGCTACTTGATGTCT	23077
rs748955497	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77300429	ACTTCCAAATTTCAC[A/G]TAATGCTCACAAAAC	23077
rs748957287	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77268229	ACTTGCCAAGTAAAT[A/G]ATATGAATGATCACT	23077
rs748972463	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77093709	TTAGGTTTCCTCTCA[C/G]AGCCATTCTCTCTTC	23077
rs748977792	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77205694	ATAAATTAAAATAAA[C/T]AAACTCAGAATGTTA	23077
rs748983042	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77150129	CATCCAAAATATATA[C/T]TTTTTAAATGTCTAA	23077
rs748985401	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77114039	AACTGACAAATACAG[C/T]GCTGAGATTATAATC	23077
rs748993015	snp	A/G	3.36768e-05	0.00410333	missense, nc-transcript-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087632	AGAAGCCAGTTGAAA[A/G]CCTGAAGAAATGACG	23077
rs748994491	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77288523	TAAGTCTATGGACCC[A/C]ACTTCTAGTCCCCTT	23077
rs749020281	snp	A/G	1.64751e-05	0.00287007	synonymous-codon	MYCBP2	GRCh38.p7	13:77174355	TCTGGTTTGGTTTGT[A/G]CCGTTACTGCTCAAG	23077
rs749035710	snp	A/G			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081815	TAACAGGACAACCAG[A/G]ATAATAACTGAAATG	23077
rs749056066	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77219850	AAAGGACTTCTAGGA[A/G]GTCCATGAGTGAGCT	23077
rs749065179	snp	A/G	1.7594e-05	0.00296592	intron-variant	MYCBP2	GRCh38.p7	13:77257632	AAAAACTAATGAAAA[A/G]ACAACACAAATTTTA	23077
rs749070849	snp	A/G	1.64833e-05	0.00287078	synonymous-codon, intron-variant	MYCBP2	GRCh38.p7	13:77126378	TGGGATACCTCTAAG[A/G]TTAGGGCAGCTTCTG	23077
rs749081631	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77256529	ATTCACAAATATAAC[A/G]TCAAAGAGCCACTCA	23077
rs749084857	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77177597	AAAGAGCTGAGATTA[C/T]AGGTGTGAGCCACTG	23077
rs749095631	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77073385	TAGAAGAAAACATTC[C/T]CCAATCTTATTAAAA	23077
rs749105386	snp	C/G/T	6.59201e-05	0.00574078	missense	MYCBP2	GRCh38.p7	13:77180284	TTCTCCAGAACTTCA[C/G/T]GGAAGCTTGTCATCC	23077
rs749105458	snp	A/G	5.01962e-05	0.00500955	intron-variant	MYCBP2	GRCh38.p7	13:77169592	AAAAAAACATTCAAA[A/G]TTATAGAATTAAATT	23077
rs749114685	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77236327	CTCATGTGTAGACAA[C/T]GGGTAATTCAGAGTT	23077
rs749116734	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77151923	TACCACTTTAGTTCT[A/T]CAGCAGGTATCACCA	23077
rs749117031	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77184101	GTCACTGATTTTAAA[C/T]CTTTCTTCTTCATAT	23077
rs749117195	snp	C/T	1.66297e-05	0.0028835	intron-variant	MYCBP2	GRCh38.p7	13:77224428	AATAACTCTGGATCT[C/T]CAAATGAAAAGTTAG	23077
rs749124261	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77312275	GAAATGCTGCATCTT[C/T]AGGAATGAAGAAAGA	23077
rs749125293	snp	C/T	1.71672e-05	0.00292973	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77082017	GCGATATATAAGCAA[C/T]ATACGAAATAATTAT	23077
rs749130429	snp	A/C	1.6517e-05	0.00287372	intron-variant	MYCBP2	GRCh38.p7	13:77065977	CACTGCCAAAACAGA[A/C]GAATGGGAACTTACT	23077
rs749147950	snp	C/T	1.7187e-05	0.00293142	missense	MYCBP2	GRCh38.p7	13:77273500	CAAGCATGGCTTCCA[C/T]TGTTGGTGAGGATAG	23077
rs749153002	snp	A/G	1.64749e-05	0.00287005	missense	MYCBP2	GRCh38.p7	13:77251268	TTGTGCATGCCTGGA[A/G]GGCACATCATAGACT	23077
rs749168460	snp	A/G	1.65105e-05	0.00287315	synonymous-codon	MYCBP2	GRCh38.p7	13:77189035	TGAAGCACTGCCATC[A/G]CTGGTTGGAAGTCTA	23077
rs749194357	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77298063	AAAGTCCAAAAGCAC[C/T]GACATCGTTTAAAAG	23077
rs749197747	snp	C/T	4.96028e-05	0.00497985	intron-variant	MYCBP2	GRCh38.p7	13:77267838	TGACTACTTGAAACA[C/T]ACCTGGTAACATCAC	23077
rs749206346	in-del	-/A	3.77053e-05	0.0043418	intron-variant	MYCBP2	GRCh38.p7	13:77191851	AAACAATATTTTCTT[-/A]ACTTCTCTGTCACAT	23077
rs749208862	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77192942	AAGGCCAGCCTGGTC[A/G]GCATGGTAAAACCCC	23077
rs749210589	in-del	-/CTGA			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291346	CCCCTACTTAGTAGG[-/CTGA]CTAAAATTTAAAAAG	23077
rs749211687	in-del	-/ATGT			intron-variant	MYCBP2	GRCh38.p7	13:77110014	AATTGATTGTAAAAC[-/ATGT]GTGTTTGAACAACAT	23077
rs749235738	snp	A/C	1.67069e-05	0.00289019	missense	MYCBP2	GRCh38.p7	13:77093332	ATTTTCATGATGATG[A/C]CTGCATTAAATCAAA	23077
rs749236596	in-del	-/C			intron-variant	MYCBP2	GRCh38.p7	13:77096037	CCATAGAGAGAATAA[-/C]AGACAATTAATAATA	23077
rs749244528	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77143158	TCAAAGTTAATGGTT[A/G]TGATGATTACTTCTA	23077
rs749255277	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77247888	GCATATACAAAAATT[A/C]ACTCAAAATGAATCA	23077
rs749258252	snp	C/T	1.65081e-05	0.00287293	missense	MYCBP2	GRCh38.p7	13:77097711	TTAGACTTCATTGTG[C/T]TATGCATGGACATTT	23077
rs749264884	snp	A/G	1.64942e-05	0.00287173	synonymous-codon	MYCBP2	GRCh38.p7	13:77180157	TGACGCTGTCAGTTC[A/G]CTGACAATGCTGGCC	23077
rs749270730	snp	A/G	1.66927e-05	0.00288895	missense	MYCBP2	GRCh38.p7	13:77262120	GCTGACTCCTCATCA[A/G]ATCCTGTACCTGAAA	23077
rs749287508	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77283896	GAGCCAGACCCTGTC[C/T]CAAAATGAAAATAAA	23077
rs749295739	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77239150	GAGCCCAGAGTTCTG[A/G]TCATCTATGAAAAAC	23077
rs749297585	snp	C/T	1.65151e-05	0.00287355	missense	MYCBP2	GRCh38.p7	13:77088882	GGGCCTGTTTCATTG[C/T]TATTTCAAGACCTTC	23077
rs749301878	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77198283	TTTAAATTTTTACTT[C/T]ATTCATTCTTACATT	23077
rs749304590	snp	C/G/T	3.29469e-05	0.00405864	missense	MYCBP2	GRCh38.p7	13:77150858	GATGCAGCTGTTACT[C/G/T]CAGGACTGCCAGGAA	23077
rs749321818	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77047608	CAGTTGGGGAAAAAA[A/G]GTCAAGCTGCAGGCA	23077
rs749326523	in-del	-/TC			intron-variant	MYCBP2	GRCh38.p7	13:77147736	GTATTTTCTATTTCA[-/TC]TCACTCTCCCTCAAA	23077
rs749327883	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77221819	CCCTCAGCATCCATG[C/G]GGAATTGGTTCCAGG	23077
rs749352074	snp	A/G	1.70822e-05	0.00292247	intron-variant	MYCBP2	GRCh38.p7	13:77061330	AAAGAACAGGGAAAA[A/G]TATGCTTATTTATCA	23077
rs749353446	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77067101	TCAAATCTATAAATA[G/T]CTTCCTATATGATTT	23077
rs749354058	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77274127	TATATCATTAACATA[A/G]TAGCAATTCACACTT	23077
rs749363153	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77288989	AAACAGTTTCTCTTT[C/T]ATGCCCAATATTTTA	23077
rs749382135	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77306895	CGGAAAGATTGCAAC[A/G]AGAACATGTGTATCA	23077
rs749386547	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77124933	TTCAATGCTCTTTCC[C/T]TAAGACAAAATGCAA	23077
rs749389327	snp	A/T	2.02374e-05	0.00318092	intron-variant	MYCBP2	GRCh38.p7	13:77089045	TTCTATTAAAGAAAA[A/T]GAAAATTATTAATTT	23077
rs749394249	snp	C/T	1.74698e-05	0.00295544	intron-variant	MYCBP2	GRCh38.p7	13:77051791	CTAAACTGTTGTTTC[C/T]AATAAAATGTTCTGC	23077
rs749402767	snp	C/T	1.66599e-05	0.00288611	synonymous-codon	MYCBP2	GRCh38.p7	13:77185334	GGTTTTTCCAATACA[C/T]TCTGCTAATTTGCTA	23077
rs749412065	snp	A/G			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77083541	TACACATACATATAT[A/G]TAGGTATGTTTTGTG	23077
rs749419496	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77132717	TACCCAAAGAATTGG[G/T]TGTGTAAGTTTGAAA	23077
rs749429068	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77197046	TGTCGTGGGGGACAA[C/G]AGAAGAAAGTATTTC	23077
rs749438016	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77165857	TGAAGGATCACAAGA[A/G]TAGTCCTGGTTAACT	23077
rs749438098	snp	A/C	1.64776e-05	0.00287028	synonymous-codon	MYCBP2	GRCh38.p7	13:77243144	TTCTTCAATGTTAAC[A/C]CCGGGCACTGGGACA	23077
rs749446378	snp	C/T	1.66228e-05	0.0028829	missense	MYCBP2	GRCh38.p7	13:77169700	AAGAACTCAGCAGTT[C/T]TGGAATGTCATCAGC	23077
rs749450929	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77184122	TTCTTCATATAAGCA[A/T]TTAAGGGTATAAAGA	23077
rs749459960	snp	C/T	3.35599e-05	0.00409619	intron-variant	MYCBP2	GRCh38.p7	13:77224558	AACACACAGCTTTAT[C/T]TTTTCATTATATGCA	23077
rs749463345	snp	C/T	7.51569e-05	0.00612967	intron-variant	MYCBP2	GRCh38.p7	13:77158138	AAGAATATTTATATA[C/T]TCTTAAAAATAAAAC	23077
rs749483176	in-del	-/AT	3.32685e-05	0.00407837	intron-variant	MYCBP2	GRCh38.p7	13:77146127	AGCAGCTGACAACAC[-/AT]GTTTTGGTTATACTT	23077
rs749493794	snp	C/T	3.30295e-05	0.0040637	synonymous-codon	MYCBP2	GRCh38.p7	13:77098694	CTTTGGCTTAGGAGA[C/T]GACAACCGAGAACCT	23077
rs749496310	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77146731	AAAACAAAACTAAAA[G/T]AAATCACATCATGGT	23077
rs749501833	snp	A/G			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228244	GGCATGGTGGTTCAC[A/G]CCTGTAATCTCAGGG	23077
rs749512765	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77322325	TCACAATCCCCTCTA[C/T]TGTTTTCACTAACAT	23077
rs749520900	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77060146	TACTTAAAGAAGAAA[C/G]AGAATCAATAAAACA	23077
rs749529372	snp	A/C	1.64931e-05	0.00287163	missense	MYCBP2	GRCh38.p7	13:77098770	GATTTCAATGTCTGC[A/C]AGGTGTTATGGTTGG	23077
rs749529980	in-del	-/AA			intron-variant	MYCBP2	GRCh38.p7	13:77301438	AAAAAAAAAAAAAAA[-/AA]AAAAAAAAAAAGAGG	23077
rs749535182	snp	C/T	1.66399e-05	0.00288438	intron-variant	MYCBP2	GRCh38.p7	13:77161975	TGTGTAAATAAAGAG[C/T]TTTACTAAAATATGT	23077
rs749562473	snp	A/T	1.65471e-05	0.00287633	synonymous-codon	MYCBP2	GRCh38.p7	13:77185151	AGCCCACTGTAAGGC[A/T]GGAGTTGGGTAGAAA	23077
rs749562616	snp	C/T	1.65957e-05	0.00288055	synonymous-codon	MYCBP2	GRCh38.p7	13:77205486	ACTTTCAAACCTGTT[C/T]ACCACACTATAATCT	23077
rs749571137	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77096055	ACAATTAATAATAAA[C/G]AGTTACACAACAAAT	23077
rs749571759	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77045893	AGGGAGATTTTTGTG[C/T]AGAATGTTTTTCTAT	23077
rs749585770	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77123346	AGATGATTAACTAAT[G/T]ACAGAGAAAAATTTA	23077
rs749605593	snp	C/T	1.65384e-05	0.00287557	synonymous-codon	MYCBP2	GRCh38.p7	13:77270043	GTTTCTAATACGGGA[C/T]GTAGAATTGTATATA	23077
rs749605646	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77109377	TCTAATGCCGCAGCT[C/G]ATCTGACAGGAAGTA	23077
rs749606283	in-del	-/TAA	1.65562e-05	0.00287712	intron-variant	MYCBP2	GRCh38.p7	13:77067576	AATAGAGGCAATAAC[-/TAA]TAACCTGGAATTGAA	23077
rs749609246	snp	C/T			intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77074091	AATAGCCAAAATAAC[C/T]TAGATAAAGAACAAA	23077
rs749615485	snp	C/G	4.94173e-05	0.00497053	missense	MYCBP2	GRCh38.p7	13:77067675	TTCCTTTGGCTTTTA[C/G]CTGTACAGTGAGTGC	23077
rs749616205	snp	A/G	1.65277e-05	0.00287464	missense	MYCBP2	GRCh38.p7	13:77211988	GCAAAAATTTCTGAT[A/G]TAGCAAGTACATGAG	23077
rs749624198	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77173183	GGACTTTAACATTTT[A/T]CATTTATAAAAAATG	23077
rs749628207	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77322176	ATCCCTGAACTTTTG[C/T]TAAAATGACTACTTA	23077
rs749634769	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77247795	TTTTGACAAAGGAGC[C/T]AAGATGGTTCAATAG	23077
rs749647570	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77265901	AAGCAACATCTGCCA[C/G]TTCTGAAGACAAATA	23077
rs749659658	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77214913	ACCAAAATACTGTTA[C/T]ACAGTGCATAACTGT	23077
rs749666502	snp	A/G	3.29788e-05	0.00406058	synonymous-codon	MYCBP2	GRCh38.p7	13:77058356	GTTTTTAACACCCCC[A/G]CATGGATGGCCACAA	23077
rs749668952	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77196347	CATTCTCACATAGGA[A/T]GACACTACAGGATTC	23077
rs749687587	snp	A/C	1.65551e-05	0.00287702	missense	MYCBP2	GRCh38.p7	13:77156061	AGTTATAATTACCTT[A/C]ATATTGGGAACATGT	23077
rs749693066	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77058957	GCCACTGTACTCCAG[A/C]CTGGGCGACACAGCC	23077
rs749705050	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77278412	AAACCATAACTTCAG[C/T]GGAACACAGAAAAAA	23077
rs749737077	snp	C/T	1.6892e-05	0.00290615	synonymous-codon	MYCBP2	GRCh38.p7	13:77270314	AACTGTTCCACTGTA[C/T]CCAGAGCCTATTTTA	23077
rs749740503	snp	G/T	5.38208e-05	0.00518725	intron-variant	MYCBP2	GRCh38.p7	13:77051935	TGTGGAGAAAACACA[G/T]CTAGATTACAGCAGG	23077
rs749756153	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77137852	GCTTCCAAAAGTGCT[A/G]GGATTACAGGCGTGA	23077
rs749762439	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77264763	GGACCACAGGAACAC[A/G]TGTTAGTGATTGCTA	23077
rs749765899	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77295197	TGGAGTGCAGTGGTG[C/T]GATCTCAGCTCACTG	23077
rs749777451	snp	A/G	6.62625e-05	0.00575559	missense	MYCBP2	GRCh38.p7	13:77211294	ATTTAAATGGAGGAG[A/G]TTCTGATATAGAAGC	23077
rs749786953	in-del	-/AGTG	1.70764e-05	0.00292197	intron-variant	MYCBP2	GRCh38.p7	13:77051198	CAGACACAAGATCAT[-/AGTG]AGACTATTTCAATCA	23077
rs749788213	snp	A/G	1.85996e-05	0.0030495	intron-variant, synonymous-codon	MYCBP2	GRCh38.p7	13:77118440	ATCAAAGATGGAAGG[A/G]GCTGGGAGATTGGGT	23077
rs749789881	snp	G/T			upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77328270	GTTTTAGGGTGGAAG[G/T]TTGCTGAAAGCAATG	23077
rs749794357	snp	A/G			synonymous-codon, nc-transcript-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087589	CCACAGAATATCATG[A/G]AGAGAAGTGGTTTGG	23077
rs749809307	snp	G/T	1.6507e-05	0.00287284	intron-variant	MYCBP2	GRCh38.p7	13:77176680	ACTCTTAATTTTATT[G/T]TATGAACAATTTTGA	23077
rs749814891	snp	C/T	1.87219e-05	0.00305951	intron-variant	MYCBP2	GRCh38.p7	13:77278737	TTTTAAATGCTTCAC[C/T]GAATGAGCCTTGGCT	23077
rs749831996	in-del	-/A	0.000130703	0.00808297	intron-variant	MYCBP2	GRCh38.p7	13:77264032	AAGTATTTATATTAC[-/A]ATACAAGCAAACACC	23077
rs749834392	snp	A/G	0.000129149	0.00803479	intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326430	GGCATGGGGCGCAAG[A/G]AAGGGCGGCATGGGG	23077
rs749840139	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77314425	ACATCTACATGGTGG[A/G]TTATTCAGTGGTAAG	23077
rs749854833	snp	C/T			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228965	TACCACAGAACACAG[C/T]GAGTACTTGGAGCAA	23077
rs749867541	snp	A/G	1.6528e-05	0.00287467	missense	MYCBP2	GRCh38.p7	13:77068618	AGAAGAGATCCTGAA[A/G]CAGGGTTAGCTGTTG	23077
rs749872511	in-del	-/CT			intron-variant	MYCBP2	GRCh38.p7	13:77182038	CAAAATTTTCTGTCA[-/CT]CTGTCATTTAAATTG	23077
rs749875948	snp	A/G	1.71835e-05	0.00293111	intron-variant	MYCBP2	GRCh38.p7	13:77121334	GTAATAAAAAATATT[A/G]AAGTTAGGTAAGTAA	23077
rs749877992	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77088697	TGATTTTTATAGGAA[C/T]ACTTAATACTTTTAA	23077
rs749880088	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77072761	GGCAATAAATCCAGA[A/C]ACTTAGATGAAATGG	23077
rs749890954	in-del	-/A	1.68272e-05	0.00290057	intron-variant	MYCBP2	GRCh38.p7	13:77224409	AAAAGAAAACAGAAG[-/A]AAAAATAACTCTGGA	23077
rs749891594	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77119043	TTTTTAAGTTGTTAC[C/T]GCCAAAGAAATTCTA	23077
rs749891755	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77104316	TTAAGAAATCATTCA[A/T]TGTAAAGTATGAGTA	23077
rs749895708	in-del	-/AAA			intron-variant	MYCBP2	GRCh38.p7	13:77266748	CAGGACTTGTAATGA[-/AAA]AAAAAAAAAAAAAAA	23077
rs749908399	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77053939	GTCCTCATGGAACTT[A/G]TCAAGTAGGGCAGAG	23077
rs749909138	snp	A/C	4.62353e-05	0.00480786	intron-variant	MYCBP2	GRCh38.p7	13:77270588	TTTTTAAATGTTACA[A/C]ACACAGAACAAAGAT	23077
rs749913490	snp	C/T	1.64808e-05	0.00287057	intron-variant	MYCBP2	GRCh38.p7	13:77059508	ATGGGATGGCCTGTG[C/T]CACTATATACTCACC	23077
rs749918506	snp	A/G	1.6727e-05	0.00289193	missense, nc-transcript-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087581	ACAAAATGCCACAGA[A/G]TATCATGGAGAGAAG	23077
rs749922901	snp	C/T	1.66535e-05	0.00288556	synonymous-codon	MYCBP2	GRCh38.p7	13:77181863	CGTGTGACACAGAGC[C/T]GACATAACAGCTGCA	23077
rs749931297	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77223419	AAATTCTTTGCATAT[A/C]TAATCCTGTCTTGGC	23077
rs749932287	snp	C/T			synonymous-codon	MYCBP2	GRCh38.p7	13:77260471	TCCAAACATGTAGAG[C/T]TCTCCATCTTTAGAA	23077
rs749940951	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77154183	ATAATATGATATTAA[C/T]ACATTAAACATCAGT	23077
rs749941042	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77281345	TTTTTAATACCTCTT[C/T]AGAAAAATGTTCTGA	23077
rs749942099	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77060475	CTAACTCCAACACTG[C/G]AAGTTCGTGTCAGTC	23077
rs749949665	snp	A/G	4.95266e-05	0.00497603	missense	MYCBP2	GRCh38.p7	13:77098671	CTAGACCTATTGGCT[A/G]GGAGAGTCTTTGGCT	23077
rs749951611	snp	C/G/T	5.08111e-05	0.00504018	intron-variant	MYCBP2	GRCh38.p7	13:77096514	AATAAATATTTAACA[C/G/T]TCCAAGTGTCCTTAA	23077
rs749957685	snp	A/G	1.6591e-05	0.00288015	intron-variant	MYCBP2	GRCh38.p7	13:77059629	GTGGTGGGTTTGCCT[A/G]GGTTCAAGCAGAAAA	23077
rs749958127	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77173124	ATGAAGGCTAGGGAT[A/G]TAAACTTGGGAGCTA	23077
rs749960159	snp	C/G/T	3.29713e-05	0.00406015	missense	MYCBP2	GRCh38.p7	13:77261305	TTTGTAATTGGTAGC[C/G/T]CAACCCATTTTCCTG	23077
rs749968122	snp	C/T	1.65795e-05	0.00287914	missense	MYCBP2	GRCh38.p7	13:77097436	CACACAGTTCACAGA[C/T]GGTATCTTTCTCTGG	23077
rs749968939	snp	A/G	1.65026e-05	0.00287246	synonymous-codon	MYCBP2	GRCh38.p7	13:77205283	AGTATATTCTCCTCT[A/G]CCTCCAAACAGACCA	23077
rs749983706	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77247431	GAAAGAAATTAAAGA[C/T]GACATAAGTAGAAAC	23077
rs749993028	in-del	-/AT			intron-variant	MYCBP2	GRCh38.p7	13:77073271	TGAAGAAAGAGAAAC[-/AT]ATAAAGGTACCACTG	23077
rs750002329	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77090389	ATCAAAGCCAAATTG[A/G]TAATCTCTCTTTAAA	23077
rs750030432	snp	C/T	1.75222e-05	0.00295986	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081674	AAACAAATATAAGTA[C/T]TTATGATACTTAAAA	23077
rs750035949	snp	A/G	4.94173e-05	0.00497053	synonymous-codon	MYCBP2	GRCh38.p7	13:77168539	CTGGTTTCCTGTGGT[A/G]CTATCTGTCGACTGA	23077
rs750036858	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77124633	GGACTCATAACTGGG[C/T]ATGAAGAAATAAACA	23077
rs750052702	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77273832	TTCCCCAAAAGTTAA[A/G]ATATTTATGTAACAA	23077
rs750053355	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77133619	CTTCTCTACTTCTAC[A/G]GATTAAGTGCTGCCT	23077
rs750063268	snp	A/G	1.6486e-05	0.00287102	missense	MYCBP2	GRCh38.p7	13:77166478	ATCAACAAACGAAGG[A/G]CATCTTCTGACTGTG	23077
rs750070333	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77199087	AGCTCCCAGCGTGAG[C/G]AACACAGAAGACGGG	23077
rs750074082	snp	C/T	1.6766e-05	0.00289529	intron-variant	MYCBP2	GRCh38.p7	13:77217802	ATTATAAGGCAATGG[C/T]ATAATGCAATATTAT	23077
rs750076640	snp	A/C	1.67486e-05	0.00289379	missense	MYCBP2	GRCh38.p7	13:77270505	CCAAAACTGCTTGTA[A/C]ACTTCTCTGTAGCGA	23077
rs750080976	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77132282	AGCTGTGACTGCTAA[G/T]TGTTATTAGGCAAAA	23077
rs750084421	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77117422	TAAAGTAATGAATAA[C/T]ATCATTTGCTAGCTA	23077
rs750090607	in-del	-/TAC	3.24554e-05	0.00402823	intron-variant, splice-donor-variant	MYCBP2	GRCh38.p7	13:77118337	TAAGGCTGACAGACT[-/TAC]TCTGAAGCTGAGGCT	23077
rs750097276	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77306236	GTAAACTGAAGCTTT[C/T]CCATAGAAGCCAGAT	23077
rs750100028	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77309031	CAAATGGATGCCAAA[C/G]GGATATGGCTAGGAC	23077
rs750112523	snp	A/G	1.66158e-05	0.0028823	intron-variant	MYCBP2	GRCh38.p7	13:77168674	TAAAAATATGGTTAA[A/G]TGAGATACACGTGAA	23077
rs750123167	snp	C/T			missense	MYCBP2	GRCh38.p7	13:77093322	AGCCCACAAAATTTT[C/T]ATGATGATGCCTGCA	23077
rs750137623	snp	C/G			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77082949	TTACTATTTAAAGAG[C/G]TTTTTTTGGAGCATT	23077
rs750147461	snp	C/T	1.6557e-05	0.00287719	intron-variant	MYCBP2	GRCh38.p7	13:77157895	AGAAATGAAGAAAGA[C/T]GAAAGCCCTAAAATA	23077
rs750151447	snp	A/G	2.13195e-05	0.00326485	intron-variant, missense	MYCBP2	GRCh38.p7	13:77118385	GCTGTCCGAACACAA[A/G]TGGGCTGTGTACTAG	23077
rs750151610	snp	C/T	1.64822e-05	0.00287068	missense, utr-variant-5-prime	MYCBP2	GRCh38.p7	13:77288328	AAGCAGAAGGATTGC[C/T]ATGTAGTTTGATATC	23077
rs750165165	snp	A/G	1.65105e-05	0.00287315	missense	MYCBP2	GRCh38.p7	13:77098143	TTGAAAAGAAAACTC[A/G]ATTTTTCTTTTTTGG	23077
rs750172424	snp	C/T	1.65209e-05	0.00287405	missense	MYCBP2	GRCh38.p7	13:77095578	GGGTCTTGACTTGCA[C/T]TGGTTTTCTCCTAGA	23077
rs750183676	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77045910	GAATGTTTTTCTATA[A/C]GTAAAAACATTTAAG	23077
rs750190664	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77196800	CACGTGGAGACACAG[C/T]GTAGGCTGTTGTACA	23077
rs750193649	in-del	-/G	1.68997e-05	0.00290682	intron-variant	MYCBP2	GRCh38.p7	13:77061130	TTAATCTTTTTTTGT[-/G]GGGTTTTAAAGGCAT	23077
rs750204840	snp	C/T			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77079144	CATTCCCTCTCCTTA[C/T]TCAAAGTCTAAATAT	23077
rs750206105	snp	C/T	1.6495e-05	0.0028718	synonymous-codon	MYCBP2	GRCh38.p7	13:77098238	TTTCAGTGGTGCTTT[C/T]CCAATGCTAAAATGA	23077
rs750212048	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77287580	GCAGAAGTTCAGTTG[C/G]TTCATAGGTGATTTT	23077
rs750213355	snp	A/G	3.33684e-05	0.00408449	missense	MYCBP2	GRCh38.p7	13:77166353	CCAAAACCATAGTAG[A/G]CCACCCAGAGGATCC	23077
rs750213456	snp	A/C	1.66751e-05	0.00288744	intron-variant	MYCBP2	GRCh38.p7	13:77176485	ACAATAGAAACATTC[A/C]GTTGAAACTACCTTT	23077
rs750219025	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77059656	AAAAATAAAAATCCT[C/T]CTTATGGATGTTTTC	23077
rs750248850	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77047052	CAACAAATATTTACC[A/G]CATGCCTAATATATG	23077
rs750255259	snp	A/G	1.66067e-05	0.00288151	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77077396	GATCAACCTGGTTGA[A/G]TAGAAAAGAGGCAGG	23077
rs750264676	snp	C/G			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081357	TTGTTGCTAAATTCA[C/G]AAATGAAAGTGCATG	23077
rs750265326	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77063384	CTAACATGGTGAAAC[A/C]CAGTCTTTACTAAAT	23077
rs750276437	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77197839	CTTAGCCCACTCACT[C/G]GATAATTGAATACAA	23077
rs750279971	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77216140	GGGCATGTCACAAGA[A/G]TACAGGAGCCAACTT	23077
rs750284876	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77115684	AAAACTATGATTCGG[-/A]AAAAAAAAAACCAAA	23077
rs750295051	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77297558	TAACTAATTTAGTAA[C/T]AGCAGTGACAAAAGA	23077
rs750307897	snp	A/G	1.92129e-05	0.00309936	intron-variant	MYCBP2	GRCh38.p7	13:77185070	TAAGCAATATATCAG[A/G]TTTTCAACTAACATT	23077
rs750315739	snp	A/T	3.30033e-05	0.00406209	intron-variant	MYCBP2	GRCh38.p7	13:77050993	TAAAATATTAAAAGC[A/T]TACCTGCAGGACAGT	23077
rs750319848	snp	C/T	1.65474e-05	0.00287636	intron-variant	MYCBP2	GRCh38.p7	13:77174300	TCCGTTATCTCTATA[C/T]ATTCACCCACCTATA	23077
rs750321479	snp	A/G	3.36961e-05	0.0041045	intron-variant	MYCBP2	GRCh38.p7	13:77140186	AGGCAAAGATAAACA[A/G]TGAGGTAGGAAGAAC	23077
rs750336835	snp	C/T	5.01979e-05	0.00500963	intron-variant	MYCBP2	GRCh38.p7	13:77088789	GAATCATCACATGAT[C/T]TGTATAATCAATGAA	23077
rs750338862	in-del	-/T			intron-variant	MYCBP2	GRCh38.p7	13:77314290	AAAAGAAAATGTATG[-/T]CCACACAAAAACCTG	23077
rs750338911	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77145019	TTTAGTGAATCATTT[C/T]GATTAGCACACAAAC	23077
rs750369925	snp	A/G	3.303e-05	0.00406373	intron-variant	MYCBP2	GRCh38.p7	13:77243031	AAAGTGGATTTTCAT[A/G]TACTTTTTCTCTGTA	23077
rs750374422	snp	C/T	3.29462e-05	0.00405857	synonymous-codon	MYCBP2	GRCh38.p7	13:77140855	CCTAACCTTATTAGG[C/T]TGAGGTTCAGACTTT	23077
rs750374488	in-del	-/ACACAC			intron-variant	MYCBP2	GRCh38.p7	13:77245747	AGAACGTAAAGTAAC[-/ACACAC]ACACACACACACACA	23077
rs750376825	snp	A/T	1.88816e-05	0.00307253	intron-variant	MYCBP2	GRCh38.p7	13:77262021	TCTTAAATCAGAGAA[A/T]GCTCATTTTTAATCC	23077
rs750399820	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77266685	TTAAAAGTATTTTTT[A/C]ATATTATTGTCATTA	23077
rs750402639	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77237536	TAACTAGAAATAAGT[A/G]AAACTTGATTAGAAG	23077
rs750402764	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77256805	ATTTAGTACAGCCAC[C/T]CTGGAGAGAACAGTA	23077
rs750405551	snp	C/T	1.66358e-05	0.00288402	synonymous-codon	MYCBP2	GRCh38.p7	13:77051151	AAAGTCTGTGCCATG[C/T]TTGGGACACATCTAT	23077
rs750406888	snp	C/T			intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77074988	CCAATGCTGGCAGAC[C/T]GCTTGAGCCCAGGAG	23077
rs750413277	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77058856	CAGGCATGGTGGCGC[A/G]CGCCTGTAATCCCAG	23077
rs750427150	in-del	-/AAG			intron-variant	MYCBP2	GRCh38.p7	13:77165806	GCAGGTCAGAGTGGA[-/AAG]AAGAAGTTTCTGAAA	23077
rs750446110	snp	C/G			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77085075	TGTTACTTACTATAA[C/G]AACTAATGCTGACAC	23077
rs750450793	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77301716	AAATATGTGGCAGAC[A/C]CATAATCAAGAGAAA	23077
rs750462178	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77150577	AATCCTCTCTGAAGA[C/T]AGGATAACATCATCT	23077
rs750472558	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77135326	TGAAGTAAGAAGGGA[C/G]AAAGATAGTTTTTCC	23077
rs750482981	snp	C/T	3.31978e-05	0.00407404	missense	MYCBP2	GRCh38.p7	13:77169682	GCATGGAAAACAGAC[C/T]GGAAGAACTCAGCAG	23077
rs750489318	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77254918	TATCCATGTTTCTGC[-/A]AATAACAATATTTCA	23077
rs750505177	snp	C/T	0.000132266	0.00813116	synonymous-codon, intron-variant	MYCBP2	GRCh38.p7	13:77126468	GAATGGCATATCTTG[C/T]TCTTGCATTGTTGCT	23077
rs750505382	snp	C/T	1.6516e-05	0.00287362	missense	MYCBP2	GRCh38.p7	13:77095559	ATGGTGGGCAAGGCA[C/T]GAGGGGTCTTGACTT	23077
rs750510405	snp	A/G/T	4.95105e-05	0.00497526	missense, synonymous-codon	MYCBP2	GRCh38.p7	13:77139196	CCACCTTTTACTTAC[A/G/T]TCAACAGGGACCAGA	23077
rs750514693	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77225736	GGAATTTTGAAAAGA[C/T]AGACTATATACTTCC	23077
rs750525627	snp	A/G	1.6898e-05	0.00290667	intron-variant	MYCBP2	GRCh38.p7	13:77068878	TATAGGGTTAGTTTG[A/G]TTTACTACTCCTAGC	23077
rs750528525	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77242403	ACAGGCGTGAGCCAC[C/T]GTGCCTGGCCAGTTA	23077
rs750531417	snp	C/T	1.64939e-05	0.0028717	synonymous-codon	MYCBP2	GRCh38.p7	13:77098763	CCCATCAGATTTCAA[C/T]GTCTGCAAGGTGTTA	23077
rs750533447	snp	C/T	0.000389887	0.0139568	intron-variant	MYCBP2	GRCh38.p7	13:77180357	TAAGGTATTGTTTTA[C/T]TTTCCTTCATAGGAG	23077
rs750538572	snp	C/T	5.05157e-05	0.00502546	intron-variant, nc-transcript-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77083023	AGGATATGTGGATAC[C/T]AAAATTACCTCAGGG	23077
rs750540874	in-del	-/TAAAA	1.66626e-05	0.00288635	intron-variant	MYCBP2	GRCh38.p7	13:77064584	GATACACACCAAATT[-/TAAAA]TAAAACAAAACAAAA	23077
rs750548628	snp	A/C/T	0.000167516	0.00915064	intron-variant	MYCBP2	GRCh38.p7	13:77224555	CAAAACACACAGCTT[A/C/T]ATTTTTTCATTATAT	23077
rs750566979	snp	A/G			intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326016	GGAAGGAATGTCATG[A/G]GAGAGGCGGCACGTG	23077
rs750567360	snp	C/T	1.64735e-05	0.00286993	missense	MYCBP2	GRCh38.p7	13:77150847	CAGTATTAGAAGATG[C/T]AGCTGTTACTGCAGG	23077
rs750582440	snp	A/C/G	3.33385e-05	0.00408269	synonymous-codon, missense	MYCBP2	GRCh38.p7	13:77057088	GAATATGTGACTACA[A/C/G]TCCAGCTTAAATAAA	23077
rs750592268	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77112554	CTTCAGCCTCTCAAG[C/T]AGCTAGGATTACAGG	23077
rs750596459	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77305056	CTCGGATGGCTTTGT[G/T]GGTGAATTCTTCCAA	23077
rs750599251	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77319758	TACAGTGCATGCCAA[A/G]CGTTATCAGTATTAG	23077
rs750611458	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77220258	AAAAAGGGTGAAAAA[A/G]GAGTAAAAAAGTAGA	23077
rs750622138	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77198985	TCCCTTCTTACAGAA[G/T]TTTGATTTTTTTAAT	23077
rs750637787	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77162060	AAAAAAATAATTCTG[C/T]TATTCCAGATTGAAA	23077
rs750645370	in-del	-/ACAC			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77227482	CACACACACACACAT[-/ACAC]ACACACACACACACA	23077
rs750647529	snp	C/T			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291025	ATTTAAAGACTTAAA[C/T]AAATGGAGACATATA	23077
rs750658616	in-del	-/T			intron-variant	MYCBP2	GRCh38.p7	13:77241111	TTAGCTAGTGGAGGA[-/T]TTTTTTTTTTAACTT	23077
rs750662803	in-del	-/T	1.85262e-05	0.00304348	intron-variant	MYCBP2	GRCh38.p7	13:77189095	GAAAGTCCAATGTCA[-/T]TTTTTTCTTTTTAAA	23077
rs750666224	snp	C/T	1.67016e-05	0.00288973	intron-variant	MYCBP2	GRCh38.p7	13:77150976	ATTATAGAAACCAAA[C/T]ACCATTATTATTTAA	23077
rs750670510	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77149555	GTAAGTGCTAATGAT[A/T]CCTGAATCCTTTTCT	23077
rs750671589	snp	A/G	3.29506e-05	0.00405884	synonymous-codon	MYCBP2	GRCh38.p7	13:77058275	CATGCACATGTCATC[A/G]GCGTCTTGCTTCAGG	23077
rs750680701	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77255804	AGTCTGACATCAAAG[C/T]CTCAAAACAGAAAAA	23077
rs750680912	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77099234	ACTATTTTCATGGAC[A/G]CAAAACAACAGGTTG	23077
rs750692290	snp	A/G	1.65732e-05	0.00287859	synonymous-codon	MYCBP2	GRCh38.p7	13:77190287	CTGACCCGCATTAAC[A/G]TCTGTACCATTATTT	23077
rs750702292	snp	A/C	4.94295e-05	0.00497115	synonymous-codon	MYCBP2	GRCh38.p7	13:77180262	TAGCACAACAATGAC[A/C]AGCATTTTCTCCAGA	23077
rs750710631	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77305976	TTTCCACTTAGGCAT[A/G]GGAGGAAAATGCAAG	23077
rs750711204	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77113454	CACCATAACCTAGCA[A/C]AGAGTAGATACTTAA	23077
rs750719931	snp	A/G	1.66563e-05	0.0028858	synonymous-codon	MYCBP2	GRCh38.p7	13:77061740	ATTTCCACAGACATT[A/G]CATAAAATGATTGCT	23077
rs750724021	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77318479	ACAAATACTGGGCCA[G/T]GCGCAGTGGCTCACG	23077
rs750738635	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77129448	AGCTCTCCATGGATA[C/T]AGTGTGTCATGCCAT	23077
rs750739768	snp	A/G			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77077076	TAATAAGTTTCACAA[A/G]ATATTTTGTTACACT	23077
rs750745475	snp	A/G	1.93063e-05	0.00310689	intron-variant	MYCBP2	GRCh38.p7	13:77263625	AAAATTAAAATATAG[A/G]GAAAACACTTAATTT	23077
rs750754868	in-del	-/AT	0.000200163	0.0100021	intron-variant	MYCBP2	GRCh38.p7	13:77090270	GTTTCTAAACTGTAC[-/AT]GGAACAATGCAACAG	23077
rs750756672	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77219476	TTTTTTTTTTTAATG[A/C]TAAGAGATTTGAGGA	23077
rs750778643	snp	C/T	0.000132952	0.0081522	intron-variant	MYCBP2	GRCh38.p7	13:77164592	GTTTGAATGATAATA[C/T]GGATTATCAACAAAA	23077
rs750782053	snp	G/T	1.65048e-05	0.00287265	missense	MYCBP2	GRCh38.p7	13:77097776	TTCATGCAGAGGTGG[G/T]TCCTTAAGCATAGAC	23077
rs750783230	snp	A/T			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77078622	GACTGGGGAACATTT[A/T]GGAAAACAGGTGAGA	23077
rs750795057	in-del	-/T			intron-variant	MYCBP2	GRCh38.p7	13:77219459	AGCTGAAGGAGAGGA[-/T]TTTTTTTTTTTTAAT	23077
rs750795266	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77255510	AGTTCAGACTTCTTA[C/T]AAAACATAATCTGAA	23077
rs750798565	snp	C/T	1.66208e-05	0.00288273	synonymous-codon	MYCBP2	GRCh38.p7	13:77263703	GATACCACAGGCATG[C/T]AAGCATTTTCTAGCC	23077
rs750799886	snp	A/G	0.000115377	0.00759443	missense	MYCBP2	GRCh38.p7	13:77144462	ATTTCAATGCCATCA[A/G]TGGTAACATGAAGAG	23077
rs750805477	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77178132	TTTATCATTCTAAAT[C/T]CACAAATCAATGTCA	23077
rs750809858	snp	C/T	1.69622e-05	0.00291219	synonymous-codon	MYCBP2	GRCh38.p7	13:77051916	TTCACCACCAAAATA[C/T]GCCTGTGGAGAAAAC	23077
rs750811197	snp	A/C	1.65534e-05	0.00287688	missense	MYCBP2	GRCh38.p7	13:77090126	TCTCCACTGTTAACT[A/C]TTCTTCTAGGAATAG	23077
rs750831706	snp	C/T	1.79978e-05	0.00299976	intron-variant	MYCBP2	GRCh38.p7	13:77185427	AAAATATTAAATATG[C/T]ATGAAAACAATCAAT	23077
rs750838596	snp	C/G	1.65217e-05	0.00287412	intron-variant	MYCBP2	GRCh38.p7	13:77171471	TCTAAAATATGACTA[C/G]TGAGAAAGAAAAAAT	23077
rs750851054	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77061852	AGACTCTCATACAAA[G/T]TGAATATAATTTATT	23077
rs750854202	snp	C/T	1.65247e-05	0.00287438	intron-variant	MYCBP2	GRCh38.p7	13:77062593	ACAAAATTCTGATCT[C/T]ACCATTTGTTTTTGT	23077
rs750861594	snp	G/T			missense	MYCBP2	GRCh38.p7	13:77270352	CATCCTTGCATAATA[G/T]ATAAAGAAAAAATCC	23077
rs750888981	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77192063	CCTTAAATGTTATAA[A/C]ACTTTCATATTAAAA	23077
rs750892882	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77297462	AAAAAAGGATGAAGT[C/T]GGGGGGAAGAGGGAA	23077
rs750897369	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77054883	TGGGATTACAGGTGT[C/G]AGCCACTGTGCCCGG	23077
rs750897584	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77298797	TGCCATAAAAGTAAA[A/G]AGAAAGAGAAAGATT	23077
rs750916676	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77101873	TATTACTAAAAATTG[C/T]ATGTTGTGGCTGCTC	23077
rs750926019	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77155003	TGTACTTAACATATG[A/C]TATTACATAGACACT	23077
rs750931604	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77208613	AAATCTAACTTTTAG[-/A]GTAGGTATGTTTTTA	23077
rs750943187	snp	C/T	1.66457e-05	0.00288489	missense	MYCBP2	GRCh38.p7	13:77185321	TTAACAAAGTTCTGG[C/T]TTTTCCAATACACTC	23077
rs750961622	snp	C/T	1.67075e-05	0.00289023	synonymous-codon	MYCBP2	GRCh38.p7	13:77164464	CTTACCAATAGGAAG[C/T]GCTAGGTCCTTCTTC	23077
rs750962269	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77177031	GTACTTTAATTTTAG[A/G]GAATATAGAAAGATA	23077
rs750962864	snp	C/T	8.29098e-05	0.00643801	intron-variant	MYCBP2	GRCh38.p7	13:77205459	CAACATTTCCTAAAC[C/T]GAAGTATACATACTT	23077
rs750965706	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77247461	CACATCTATGTTCAT[A/G]GATTAGAAGACTTAA	23077
rs750967143	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77142524	GCCAAAGCAAACTAC[C/T]TAAAGCAGGGTTTCC	23077
rs750967185	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77125629	AGCCTGAGGTAAGAC[A/G]GAAGTCAATAAAAAG	23077
rs750967709	snp	C/T	1.76456e-05	0.00297026	intron-variant	MYCBP2	GRCh38.p7	13:77270288	GGAACTGTAAGGAAT[C/T]ACATTACCCTAACTG	23077
rs750976107	snp	A/G	1.65138e-05	0.00287343	synonymous-codon	MYCBP2	GRCh38.p7	13:77097683	ATGTTGTAAAGTTAA[A/G]GGAAGAGGAGACTTA	23077
rs751004370	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77107583	TTCCACAAAAAAATA[C/T]AAAAATTAGGCAGGT	23077
rs751007875	snp	C/T	1.6483e-05	0.00287076	missense, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081473	GACACATAGCGGGCA[C/T]TGATTCCTTTTACAC	23077
rs751015033	snp	C/G	7.56931e-05	0.00615149	intron-variant	MYCBP2	GRCh38.p7	13:77264036	ATTTATATTACAATA[C/G]AAGCAAACACCTTGC	23077
rs751015825	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77105439	AAAAAAGGTTAAGTG[A/T]CTAAAGAAATTAAGC	23077
rs751017349	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77248836	ACAGCGCATTACTCA[C/G]AATAGTTACAATGTG	23077
rs751017635	snp	C/T	1.68952e-05	0.00290642	missense	MYCBP2	GRCh38.p7	13:77205573	CATTTTTAAGTCCTG[C/T]ATAGCTGCCAAGGTA	23077
rs751044144	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77298861	CCTGCTTATAGAATC[C/T]ACTCAACTACTAGCA	23077
rs751049713	snp	C/G	8.62776e-05	0.00656745	missense, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326657	GAGCCGTCGGGAACC[C/G]GCATGAACAGCGCCC	23077
rs751053527	snp	C/T	1.64985e-05	0.0028721	synonymous-codon	MYCBP2	GRCh38.p7	13:77096330	CTCCCTTGCAGCAGC[C/T]TGTTTTTCGCGGAGG	23077
rs751057590	snp	G/T	3.34487e-05	0.00408941	missense	MYCBP2	GRCh38.p7	13:77191772	TACCACCACCCAGCT[G/T]GCAGGAGAACAGGCT	23077
rs751064998	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77068271	CACGAAAAAAAATAC[C/T]TTTTCTTTCTGGTCA	23077
rs751086535	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77212696	ATTATTTCATTTATG[A/T]TTTAAAATAAACAGC	23077
rs751087784	in-del	-/TCTATTTTCTAATAGACGGC			intron-variant	MYCBP2	GRCh38.p7	13:77091130	CCCTTGGTAAAATTA[-/TCTATTTTCTAATAGACGGC]TCTATTTTCTAATAG	23077
rs751101872	snp	A/G	0.000181439	0.00952294	missense	MYCBP2	GRCh38.p7	13:77098585	GCTTTGTCTTAACAG[A/G]AGCAGTACTTTTTTG	23077
rs751106325	snp	A/C	1.94615e-05	0.00311935	intron-variant	MYCBP2	GRCh38.p7	13:77212204	ATATTGCTGTGTAAA[A/C]AATCTAATTTTCATA	23077
rs751113009	snp	G/T			intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77325449	ATGCGGCATGTAAGG[G/T]CATGGAAAAGAAAAC	23077
rs751125583	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77056384	TACGAAGATAAGAAA[A/G]TAGGGAGAGCTTAAT	23077
rs751127355	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77225126	ATGGGAACATGTTAC[A/G]AAAACCACAGCATTC	23077
rs751129260	snp	C/T	1.68408e-05	0.00290175	intron-variant	MYCBP2	GRCh38.p7	13:77090296	CAACAGATACAAACT[C/T]AGAAGAGCTGAATGA	23077
rs751137068	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77248783	GCCCAAAAGAACTGA[A/C]AACAGGGTCTCAAAG	23077
rs751150586	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77309998	GTGCCTGTAGTCCCT[C/G]CTATGTAGAAGGCTG	23077
rs751155477	snp	G/T	1.64925e-05	0.00287158	synonymous-codon	MYCBP2	GRCh38.p7	13:77055612	CATTGCATAGCCAGC[G/T]GGGTCATTATAAAAC	23077
rs751165430	snp	A/G	2.01765e-05	0.00317614	intron-variant	MYCBP2	GRCh38.p7	13:77176672	TCCAACAGACTCTTA[A/G]TTTTATTGTATGAAC	23077
rs751177125	snp	C/T			missense	MYCBP2	GRCh38.p7	13:77096355	CGGAGGTATTTTTCT[C/T]TACAGCGATCACATA	23077
rs751178517	snp	A/T	1.7771e-05	0.0029808	intron-variant	MYCBP2	GRCh38.p7	13:77067903	GAATTCCATGTAAAG[A/T]CTAATGTTTTAAGGT	23077
rs751179862	snp	A/G	1.68715e-05	0.00290439	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081381	GTGCATGAATACTAA[A/G]ATCTGAAAAGAGCTA	23077
rs751192416	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77262349	TTGTTCCAAACCAGT[A/G]CCAAATTAATTTTTT	23077
rs751194771	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77155249	TCTTCACGCTATAAA[C/T]GAAAGAATGCATGAA	23077
rs751201671	snp	A/C	1.88078e-05	0.00306652	splice-acceptor-variant	MYCBP2	GRCh38.p7	13:77243952	CCACAACCACAGATC[A/C]TAGGGGGAAATACAA	23077
rs751211081	snp	C/T	1.64844e-05	0.00287087	missense	MYCBP2	GRCh38.p7	13:77212067	CACCTATCCAAGTAG[C/T]TTTTCTTCCATATTT	23077
rs751219664	snp	C/T	4.94907e-05	0.00497422	intron-variant	MYCBP2	GRCh38.p7	13:77144577	TGAAAAGAAATAAGA[C/T]GGATATTGGAAATTT	23077
rs751237371	snp	A/T	3.29652e-05	0.00405974	synonymous-codon	MYCBP2	GRCh38.p7	13:77177835	TATTCCAGGTTTGTC[A/T]ACTGAAAAACAGATT	23077
rs751237696	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77120349	AAAAAAAATCTTGTG[C/G]CTAGGTTTCCTTCAT	23077
rs751238365	in-del	-/A/AA/AAA	0.0135952	0.081443	intron-variant	MYCBP2	GRCh38.p7	13:77243963	ATCCTAGGGGGAAAT[-/A/AA/AAA]ACAAAAAAAAAAAAA	23077
rs751241257	in-del	-/TA			intron-variant	MYCBP2	GRCh38.p7	13:77240973	TGAACAAAGTGTTTC[-/TA]CTGATGTTCTATATA	23077
rs751274046	snp	C/T	1.64876e-05	0.00287116	missense	MYCBP2	GRCh38.p7	13:77261290	ACTATCTTTGGAGAT[C/T]TTGTAATTGGTAGCT	23077
rs751277361	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77311453	GCACATGTTGTAATT[A/G]TCCAACAATGACTGG	23077
rs751281842	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77176062	CACAATAAGAGAAGA[A/C]AAGACAGGAGCTAAT	23077
rs751302974	snp	A/G	3.32408e-05	0.00407668	missense	MYCBP2	GRCh38.p7	13:77140153	CTGTCCTTGGCCACA[A/G]ATTTTCGAACCTGAG	23077
rs751306478	snp	A/T	0.000133083	0.0081562	synonymous-codon	MYCBP2	GRCh38.p7	13:77098985	TGTAGAGGCTGGTTT[A/T]GAAGATGTTGAGATG	23077
rs751308367	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77239655	ACAGTTTACTGGCTG[C/T]ACTCCCCCAGTTTTT	23077
rs751316321	snp	C/G	3.29962e-05	0.00406165	intron-variant	MYCBP2	GRCh38.p7	13:77233131	GGGAAAGTATCCCAC[C/G]TAGGTGATAAGGAAG	23077
rs751323914	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77144774	AACTCTCAGGTGATC[A/G]TGACCTCACCTCTTT	23077
rs751325380	snp	C/T	1.65026e-05	0.00287246	missense, intron-variant	MYCBP2	GRCh38.p7	13:77233255	TAGGACCAGCAAATA[C/T]AAGGGGGCCTGAGGA	23077
rs751330952	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77133984	TCCACCCAATGCCTA[C/T]TTTCCAGCTTAGTAT	23077
rs751337068	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77198776	CTCCACTCCTGGGGT[A/G]AAGATGTCTGTTTAC	23077
rs751338630	snp	A/G	1.68136e-05	0.0028994	synonymous-codon, nc-transcript-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087558	CTGGTGCAGGAGTCA[A/G]TGATGCCACAAAATG	23077
rs751358145	snp	A/G	1.658e-05	0.00287919	intron-variant	MYCBP2	GRCh38.p7	13:77050971	ATATAGATCATAATC[A/G]TGATTTTAAAATATT	23077
rs751376742	snp	A/C	1.65236e-05	0.00287429	missense, utr-variant-5-prime	MYCBP2	GRCh38.p7	13:77288174	ACCTTTGGAAGCTTG[A/C]TAGGGGGCTCTTTGG	23077
rs751377809	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77223552	AATGAAAGACAAGTA[A/G]GAGGGACTTCAAGAT	23077
rs751383072	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77290324	CCTACAAAACTAAAT[A/G]TGTGCTTACCATATA	23077
rs751383274	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77275371	TTCCTTCACTCTCCA[C/T]ATTCTAGCCATATTG	23077
rs751387501	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77323930	TGAGATCCCTTTGAC[C/T]TCTTCCTGTCCCTGA	23077
rs751400869	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77303377	ATCAACCTGACCTAA[C/T]TGGCATACATACAGA	23077
rs751404515	snp	A/T			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77084812	GCCAGGACCCTAGGG[A/T]TATTTTTATGCAAAA	23077
rs751419386	in-del	-/AGG			intron-variant	MYCBP2	GRCh38.p7	13:77285848	GAAAAGAAAAAAGGA[-/AGG]GAAAGGAAGGGAAAG	23077
rs751436110	snp	C/G			missense	MYCBP2	GRCh38.p7	13:77068639	TTAGCTGTTGAGCCA[C/G]ATATTGCCGGCCAAC	23077
rs751445208	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77047321	TTTCTGATTCTTAGA[C/T]ACCTCATCTTTAAAA	23077
rs751447640	snp	C/T	1.64768e-05	0.00287021	missense	MYCBP2	GRCh38.p7	13:77194190	ATACATCAGTCTCTG[C/T]AAGAAGGTCACCATC	23077
rs751454254	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77297840	ACAGTTATTGAATCT[C/G]TCCACACCATCTTTA	23077
rs751468407	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77132462	AATCTTTCAGGTTCC[A/C]AAATTTGGAAAATCA	23077
rs751477770	in-del	-/A			upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77328873	GGATCTAGGATGTCC[-/A]AACTTGGCACATGAA	23077
rs751480883	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77238948	CAACATGGTGAAACC[C/T]CATCTCTAACAAAAA	23077
rs751492065	in-del	-/C	1.74912e-05	0.00295725	intron-variant	MYCBP2	GRCh38.p7	13:77061348	TGCTTATTTATCACT[-/C]TGAAAGGGAGAGTAT	23077
rs751506090	snp	A/G	1.64757e-05	0.00287012	missense	MYCBP2	GRCh38.p7	13:77158019	TGCTTTGGATTTGGA[A/G]TGGTAAATTTCCCTC	23077
rs751507688	in-del	-/TGTGTGTGTGTGTGTT			intron-variant	MYCBP2	GRCh38.p7	13:77056145	GTGTGTGTGTGTGTG[-/TGTGTGTGTGTGTGTT]TTGCTTCCTTGAGGG	23077
rs751511791	snp	C/G	2.18e-05	0.00330144	intron-variant	MYCBP2	GRCh38.p7	13:77270582	AAAACATTTTTAAAT[C/G]TTACAAACACAGAAC	23077
rs751523201	snp	C/T	1.66142e-05	0.00288216	missense	MYCBP2	GRCh38.p7	13:77140052	TATCAATTACCTCAT[C/T]AATAAAAGTGATAGT	23077
rs751530563	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77183951	TTTTTCTTCAAAAAA[A/C]CAACTTTTAGCTGTG	23077
rs751546986	in-del	-/G	0.000371603	0.0136258	intron-variant	MYCBP2	GRCh38.p7	13:77070721	TGTTGCCTTTACATA[-/G]AAAAAGAAAAAAAAA	23077
rs751556786	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77147447	CTGTATGCCTGCAAC[A/T]TTAGCAAAGAAATCA	23077
rs751562660	snp	A/G	0.00013417	0.00818943	intron-variant	MYCBP2	GRCh38.p7	13:77056959	CAAAAGAAAAAGAAA[A/G]TACATGATTTCAGAT	23077
rs751575831	snp	C/G	1.64974e-05	0.00287201	synonymous-codon	MYCBP2	GRCh38.p7	13:77059616	TTCTGAGCTACTCGT[C/G]GTGGGTTTGCCTAGG	23077
rs751576053	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77179957	GAGAGAGAAGTAACA[A/C]ATCAGAGAAAGTAGG	23077
rs751579959	in-del	-/TC			intron-variant	MYCBP2	GRCh38.p7	13:77147322	TTGTACCTGTAGCAA[-/TC]TGTTTCTTAATAAAA	23077
rs751588239	in-del	-/CATT			intron-variant	MYCBP2	GRCh38.p7	13:77117251	TCTTCTCTTAATAGA[-/CATT]CAAATTAATATTATA	23077
rs751595431	snp	C/T			intron-variant, downstream-variant-500B	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77088182	AGGAAAAATAATTTA[C/T]AAGATACAATACCAA	23077
rs751605934	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77105748	GATTCTTTTTTGGGT[A/G]TCACTAAGTTTAAGA	23077
rs751621894	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77122980	ACTGCTTCCTCTCTA[A/G]ACTAAGAATGGTCTA	23077
rs751631854	snp	A/C/T	3.31489e-05	0.00407107	intron-variant	MYCBP2	GRCh38.p7	13:77065954	TGTGTCAGCTTCCTG[A/C/T]CGCACTTCACTGCCA	23077
rs751642278	snp	C/T	1.64732e-05	0.0028699	missense	MYCBP2	GRCh38.p7	13:77150829	GCCCTCCATAAGTCA[C/T]GTCAGTATTAGAAGA	23077
rs751643906	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77214565	TTACCTTTAAAAAAC[A/G]GGAAAGGGGAAATAT	23077
rs751670927	snp	A/G	1.79242e-05	0.00299362	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081701	AAAAGCAAATCTTTC[A/G]TGATGATAAAACAAA	23077
rs751672498	snp	C/T	3.41986e-05	0.00413499	intron-variant	MYCBP2	GRCh38.p7	13:77189073	TAGACACATATAAAA[C/T]TATGTTAGAAAGTCC	23077
rs751674483	snp	A/G	1.67027e-05	0.00288982	intron-variant	MYCBP2	GRCh38.p7	13:77126304	AGAAGTCATGAAGCT[A/G]CAAGAATCCATACCT	23077
rs751681934	snp	G/T	1.64928e-05	0.00287161	missense	MYCBP2	GRCh38.p7	13:77098215	GATGCTCTCATTTCC[G/T]GTTCATCTTTCAGTG	23077
rs751683385	snp	A/G	1.65321e-05	0.00287502	missense	MYCBP2	GRCh38.p7	13:77165382	TCCAATGAAAAAAGG[A/G]CCTCATTTCCTAATA	23077
rs751684250	snp	C/T	1.65012e-05	0.00287234	synonymous-codon	MYCBP2	GRCh38.p7	13:77093278	ACGTAGATATCTCAT[C/T]TCATCCTGGAATAGA	23077
rs751688978	snp	C/T	4.96759e-05	0.00498352	missense	MYCBP2	GRCh38.p7	13:77180134	TGTATTACCTCAGAT[C/T]CCAGGGCTGACGCTG	23077
rs751692479	snp	A/T	1.65468e-05	0.00287631	intron-variant	MYCBP2	GRCh38.p7	13:77251368	ACCCTATTTGACAGA[A/T]CAATTTGTAATTTTT	23077
rs751702452	snp	A/G	0.000166694	0.00912795	missense	MYCBP2	GRCh38.p7	13:77095367	TATTACCTAGCTAAT[A/G]TCTGCAGGTAGAGAC	23077
rs751708196	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77100550	AGAGGTGACATTAGT[C/T]ATTGATGTGCAAGGG	23077
rs751721940	snp	C/T	1.66449e-05	0.00288482	missense	MYCBP2	GRCh38.p7	13:77057065	ACTCGCCGACAGCAC[C/T]GTAAGTGGAATATGT	23077
rs751727614	snp	A/C/T	4.95342e-05	0.00497645	missense, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77077173	ATCAGTCTGAATACT[A/C/T]GCAGAGTCTCAGCTT	23077
rs751730645	snp	C/T	5.05421e-05	0.00502678	intron-variant	MYCBP2	GRCh38.p7	13:77150703	ACAAATGCTGAAAAC[C/T]AAAATTTTTCTGATA	23077
rs751733881	snp	C/T			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77292870	GGCTGAGGCAGGGAA[C/T]TGCTTGAACCCAGGA	23077
rs751737248	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77172836	ATTCTGGTTAAGGGT[C/G]TATCACCTGAAATCT	23077
rs751740533	in-del	-/AG			intron-variant	MYCBP2	GRCh38.p7	13:77054588	TTGTCAATAAAGATC[-/AG]AGATTGGTAAAGTCT	23077
rs751761217	in-del	-/GCG			upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77327113	GGCCTCACAGAGCAT[-/GCG]CCACTCCTCGCACAT	23077
rs751778476	snp	A/T	1.68119e-05	0.00289926	intron-variant	MYCBP2	GRCh38.p7	13:77150705	AAATGCTGAAAACTA[A/T]AATTTTTCTGATAAG	23077
rs751785432	snp	A/G	4.9423e-05	0.00497082	synonymous-codon, utr-variant-5-prime	MYCBP2	GRCh38.p7	13:77288284	CTGCCATTCCAGAAC[A/G]CAATGGCGTACATTA	23077
rs751791846	snp	C/G			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087064	TTAGTTCTTGCTCAT[C/G]GTGTCTTGTTTGTGA	23077
rs751796000	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77136801	GTCCCTCCCTCCTCT[A/G]AAACATAACTACTGC	23077
rs751796827	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77137171	CCTGACCTTAAGGAG[A/G]CTGTCTACTACAGAT	23077
rs751800130	in-del	-/G	3.55385e-05	0.00421521	intron-variant	MYCBP2	GRCh38.p7	13:77158117	TTGCACACCTGTTAA[-/G]TAAAAAAGAATATTT	23077
rs751809739	snp	A/T	3.35926e-05	0.00409819	missense	MYCBP2	GRCh38.p7	13:77166343	CCTGGCAACACCAAA[A/T]CCATAGTAGGCCACC	23077
rs751810881	snp	C/T	1.6643e-05	0.00288465	missense	MYCBP2	GRCh38.p7	13:77263934	GGATACTTACATCTC[C/T]TGAAGCAGCTATCTG	23077
rs751822993	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77178495	ACTACGAATATATAC[-/A]GTGATATTTTTGTAA	23077
rs751827022	in-del	-/C			intron-variant	MYCBP2	GRCh38.p7	13:77217963	GGACATCCCCTAGGT[-/C]TAAAAAAAAAAAAAG	23077
rs751829071	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77241234	CAAGTTATCAATGCA[C/T]GATTCAATGTTCCTT	23077
rs751832042	snp	C/G	1.66871e-05	0.00288847	missense	MYCBP2	GRCh38.p7	13:77211189	TTACATCATATACAG[C/G]ATCAAGACACACACC	23077
rs751836766	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77306187	CACTGGATACAAGAC[C/T]AACTTTTAAAAATCA	23077
rs751837297	in-del	-/ATATT			intron-variant	MYCBP2	GRCh38.p7	13:77255535	TCTGAATATATATTC[-/ATATT]ATATATTAAAAAAAC	23077
rs751851022	snp	C/T	1.67399e-05	0.00289304	intron-variant	MYCBP2	GRCh38.p7	13:77068863	CAGAACATGTAAAAA[C/T]ATAGGGTTAGTTTGA	23077
rs751854732	snp	C/T			upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77327893	TGAAAATGTCAGATC[C/T]ATCACATATCTTGTT	23077
rs751856327	snp	G/T	4.99496e-05	0.00499723	missense	MYCBP2	GRCh38.p7	13:77273599	GAAAGTGCTGTTAAG[G/T]ACTGTCCTGTGCTGT	23077
rs751859024	snp	A/G	1.65116e-05	0.00287324	missense	MYCBP2	GRCh38.p7	13:77188961	CTTACCACTGAGACA[A/G]TTCTTGCAAAAGACC	23077
rs751868128	snp	C/T	1.66757e-05	0.00288749	synonymous-codon	MYCBP2	GRCh38.p7	13:77097467	TCCTCCTACTGCCAG[C/T]TGGGCCATCTCTCCA	23077
rs751875168	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77101746	TTTATTTTTCCAAAA[C/T]GTATTTTATATATTA	23077
rs751875645	snp	A/C	3.30721e-05	0.00406632	missense	MYCBP2	GRCh38.p7	13:77098119	TCTAAAGGCTTGGAT[A/C]CATCTCCTTTGAAAA	23077
rs751911426	snp	C/T			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77079757	CCCCAAATCTGAATA[C/T]CTAAAACCAGAAATG	23077
rs751920273	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77321022	AAACAGTCTATACTT[A/G]ACTGTGGTGATAGTT	23077
rs751930444	snp	C/T	1.73875e-05	0.00294847	intron-variant	MYCBP2	GRCh38.p7	13:77169762	AGTCAGAAGGTAATT[C/T]CATTGTACTGCATAC	23077
rs751935629	snp	A/G			synonymous-codon	MYCBP2	GRCh38.p7	13:77206728	CAAGTTCAGGACTTA[A/G]GATACTACATCTGGA	23077
rs751951712	snp	C/T	1.64765e-05	0.00287019	synonymous-codon	MYCBP2	GRCh38.p7	13:77180244	CAGGCTGTTCCTGAC[C/T]GGTAGCACAACAATG	23077
rs751958701	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77149880	ACCAAATTAAGTCAA[C/T]AGTCCCCTAAAGAGA	23077
rs751968087	snp	C/T	1.65146e-05	0.0028735	missense, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081931	ATATTGTTAATGTGA[C/T]GAAAGACGTTGCTCT	23077
rs751973267	snp	A/G	1.6649e-05	0.00288518	missense	MYCBP2	GRCh38.p7	13:77097595	CTGCACAGGAACCAG[A/G]ACTTGGAAAAATCAT	23077
rs751980082	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77050280	GCAGTGTGTGTTTTC[C/T]AGCTTTGACAACACG	23077
rs751981003	snp	A/C	1.84466e-05	0.00303693	intron-variant	MYCBP2	GRCh38.p7	13:77273701	TTCAATTATATTCAT[A/C]CAACATACGGAACAT	23077
rs751991353	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77221289	TCTGGCCTGAAACTG[C/T]CCTATATCTCTTCAG	23077
rs751994847	snp	A/C	5.0197e-05	0.00500959	intron-variant	MYCBP2	GRCh38.p7	13:77217980	AAAAAAAAAAAAAGT[A/C]AGTCAATTTCTTACA	23077
rs752017337	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77285366	CCTCCAGCCCTACGT[C/T]CTAACTCAACTATGT	23077
rs752018654	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77256974	TAGCCAAGATTTGGA[A/G]GCAACCTAAGTGTCC	23077
rs752024236	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77235970	CTGTAGAGATAAAAG[C/T]ATATCCTTCATCCTA	23077
rs752026081	snp	G/T	1.67913e-05	0.00289748	missense	MYCBP2	GRCh38.p7	13:77262063	TTTACCTTTCCATTT[G/T]CTGTTTTCATTAGCG	23077
rs752037791	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77179968	AACAAATCAGAGAAA[C/G]TAGGAGGTGGAGAGA	23077
rs752043837	snp	A/G	6.59739e-05	0.00574305	missense	MYCBP2	GRCh38.p7	13:77205338	TCGGCACTGAAACGT[A/G]TAGCTTCTACTGAAT	23077
rs752057125	snp	G/T			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291011	TGTTGCTGAGTGAAA[G/T]TTAAAGACTTAAATA	23077
rs752070758	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77284304	ACAGCCACACACTTA[A/G]GAGGAGCAACAGAGG	23077
rs752072308	snp	C/T	1.65888e-05	0.00287996	missense	MYCBP2	GRCh38.p7	13:77169670	TAAGGGGGAGCAGCA[C/T]GGAAAACAGACTGGA	23077
rs752077802	snp	A/G	1.65211e-05	0.00287407	missense, intron-variant	MYCBP2	GRCh38.p7	13:77126460	CCTCGCAAGAATGGC[A/G]TATCTTGTTCTTGCA	23077
rs752084814	snp	A/G	2.04819e-05	0.00320009	intron-variant	MYCBP2	GRCh38.p7	13:77118536	TACAACTCGTTATTC[A/G]TTAACATCCAAAATG	23077
rs752085169	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77183247	GATAAAGCTAAACTC[A/C]TAAAATTAGTTGGGA	23077
rs752100545	snp	A/G	1.65872e-05	0.00287981	synonymous-codon	MYCBP2	GRCh38.p7	13:77257807	CTGAGTTACAAAATG[A/G]CCCTTCAAATCAGTT	23077
rs752109071	snp	C/T	3.32248e-05	0.0040757	intron-variant	MYCBP2	GRCh38.p7	13:77243206	ACAACATATATGTTA[C/T]ATAATAGCTATGACA	23077
rs752109192	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77129396	GAGTAAACAACACAC[C/T]GAAGAAATTCTGTCT	23077
rs752112494	snp	C/T	1.65419e-05	0.00287588	missense	MYCBP2	GRCh38.p7	13:77098680	TTGGCTGGGAGAGTC[C/T]TTGGCTTAGGAGATG	23077
rs752119162	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77129299	ATCATCTGCAGAAGA[C/T]GCGTGCACAGTAACA	23077
rs752126230	in-del	-/A	1.64849e-05	0.00287092	frameshift-variant, intron-variant	MYCBP2	GRCh38.p7	13:77126407	TGATGTTGTGACCTG[-/A]AGGTCCCGTCTTCAC	23077
rs752128334	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77162179	ATACTCAAGAAGCAT[C/G]CATGGGTGATTTGCC	23077
rs752133964	snp	A/C	1.69255e-05	0.00290903	intron-variant	MYCBP2	GRCh38.p7	13:77090085	AGATCACTCAATATT[A/C]TTTTTTATCCTCATA	23077
rs752148778	snp	C/G	3.30524e-05	0.00406511	synonymous-codon	MYCBP2	GRCh38.p7	13:77224507	ATAACCAAATGTATA[C/G]ACATCTCCATTTTCC	23077
rs752161234	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77144679	CAATCCTACCACCCT[A/G]CCATAGTACGCTTGC	23077
rs752168468	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77226526	CACAAGTTCAACTAG[C/T]CTAAACCACTCTCAA	23077
rs752174440	snp	C/T	1.65272e-05	0.0028746	missense	MYCBP2	GRCh38.p7	13:77098384	GGAGGTTTTCCTGTA[C/T]CACATGGGGAGAGGG	23077
rs752187753	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77285502	TTAAAGAAAGAAGCT[A/G]TTGGCCAGGCACGGT	23077
rs752214211	in-del	-/CA			intron-variant	MYCBP2	GRCh38.p7	13:77223831	CCTATCACTTAAGTT[-/CA]CATGGCCACATCCTG	23077
rs752239063	snp	C/G			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77080132	AAAGTAGTTACACCA[C/G]TGGAAATTCTTAGGT	23077
rs752241394	snp	C/G	1.67967e-05	0.00289794	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77077430	CTGATTCAGCTGGAT[C/G]ACTTTTATCACTGTG	23077
rs752246219	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77313819	CTAACAATAAGAAAA[A/C]AAACAACTCAATTAA	23077
rs752256685	in-del	-/G	1.94983e-05	0.0031223	intron-variant	MYCBP2	GRCh38.p7	13:77263624	GAAAATTAAAATATA[-/G]GGAAAACACTTAATT	23077
rs752257951	snp	C/T	1.70124e-05	0.00291649	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77078919	TCACAATAGTTAATA[C/T]GCTATATTCCTGCTT	23077
rs752260002	snp	A/T	1.66147e-05	0.0028822	intron-variant	MYCBP2	GRCh38.p7	13:77066123	TTAAAAAGCCAATAA[A/T]TTATCAGTAGTAGTA	23077
rs752262389	snp	C/T	5.31646e-05	0.00515553	intron-variant	MYCBP2	GRCh38.p7	13:77262170	ATTGCATTTCTAATA[C/T]GAAGAATTCTAAATA	23077
rs752266390	snp	A/C/G	3.52232e-05	0.0041965	intron-variant	MYCBP2	GRCh38.p7	13:77211930	ACAAGAGTTTGGAAG[A/C/G]GGCATTTGTTTATTT	23077
rs752270244	snp	A/G			utr-variant-3-prime	MYCBP2	GRCh38.p7	13:77045276	CATTTTCATGGATGT[A/G]AAAATGGTCCCGTCC	23077
rs752273219	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77194422	TATGTATTTAAATTA[A/G]GAAACAAGGTTTTAT	23077
rs752281240	snp	C/T			missense	MYCBP2	GRCh38.p7	13:77096457	ATGCTATTGTAACCT[C/T]GTCCACCAGCATATC	23077
rs752283900	snp	A/C	3.32524e-05	0.00407739	missense	MYCBP2	GRCh38.p7	13:77185287	ATGCAGTGATCAACT[A/C]CTTCTGATAAAATTT	23077
rs752284428	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77319968	GAGTGCCCTCCGAAC[A/C]AACAACTGTGGGGCA	23077
rs752287671	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77271779	TAAACCTCTTTCTTT[A/T]GTAAATTGCCCAGTC	23077
rs752290620	in-del	-/AA			intron-variant	MYCBP2	GRCh38.p7	13:77069693	AACCCCGTCTGTACT[-/AA]AAAAAAAAAAAAAAA	23077
rs752291996	snp	C/T	1.64732e-05	0.0028699	missense	MYCBP2	GRCh38.p7	13:77061687	TGAGTTTTGGTTCTT[C/T]GATGAAGGTGAAGGA	23077
rs752300629	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77299319	AAATACTTCTTTCTA[C/T]GCATGATGGCATTTA	23077
rs752311219	snp	C/T	1.74394e-05	0.00295286	intron-variant	MYCBP2	GRCh38.p7	13:77180106	GTGCTTTTTATCCAG[C/T]GTCAAAATATAATGT	23077
rs752319846	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77248855	AGTTACAATGTGGAA[A/G]CAACCAAAGTGTTCA	23077
rs752322544	snp	A/G	5.6766e-05	0.00532727	synonymous-codon, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326500	GTGTCCAGCGCTGCC[A/G]CCCCCCTGGTCCCTG	23077
rs752346493	in-del	-/AT			intron-variant	MYCBP2	GRCh38.p7	13:77130408	ATTTTCCATATCCAT[-/AT]ATATATATATGGATA	23077
rs752347658	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77194023	TTGCTTAATATATAA[C/T]TTAATTTCTCAAGTA	23077
rs752347923	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77056524	ACCTTTGTACAAATG[C/T]GTCAAAATGCCAAGA	23077
rs752351188	snp	C/T	3.29533e-05	0.00405901	missense	MYCBP2	GRCh38.p7	13:77140929	GGTCTTTTACTTTTA[C/T]TTCCAGACCAGCATC	23077
rs752353530	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77300360	CAATGGTTACAGCAC[A/G]AAAGCAGCCATCGGC	23077
rs752354157	snp	A/G	1.69714e-05	0.00291298	intron-variant	MYCBP2	GRCh38.p7	13:77164448	TCCAGTATTGGCCAC[A/G]CTTACCAATAGGAAG	23077
rs752360697	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77108853	GGACTACAGGTGCCT[C/G]CCACCACACCCAGCT	23077
rs752361589	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77143846	ATACTGCAGGTAACT[C/G]TAACACAATGGTAAG	23077
rs752363979	in-del	-/AAAAC	5.56576e-05	0.00527501	intron-variant	MYCBP2	GRCh38.p7	13:77064585	ATACACACCAAATTT[-/AAAAC]AAAACAAAACAAAAC	23077
rs752364410	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77122431	CCTTGGCCGGTCGCG[G/T]TGGCTTACGCTTGTA	23077
rs752372806	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77241867	AAAAAATATAATGAT[G/T]GTTAAATGGGTAAAA	23077
rs752373276	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77107687	AGGTTGCAGTGAGCC[C/T]AGATTGCACCACTGT	23077
rs752380640	in-del	-/CCAGTAAATAATT			intron-variant	MYCBP2	GRCh38.p7	13:77252223	ACCTTTTATAAAGAG[-/CCAGTAAATAATT]TAGGCTCTGTGGCCC	23077
rs752397265	snp	A/G	3.30398e-05	0.00406434	missense	MYCBP2	GRCh38.p7	13:77270406	CATCTTCATCAACAG[A/G]TATTTCTTTTAATGG	23077
rs752403567	snp	A/G			upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77327485	GAGTTTAAGGCAGAG[A/G]AAACCATCCCAATTA	23077
rs752407102	snp	A/G	0.000412259	0.0143513	synonymous-codon	MYCBP2	GRCh38.p7	13:77144446	TTTAAAGAAAATACC[A/G]ATTTCAATGCCATCA	23077
rs752414464	in-del	-/A	0.000113414	0.00752955	intron-variant	MYCBP2	GRCh38.p7	13:77296698	TAAAAGAAAAATGGG[-/A]AAAAAATATGAATGT	23077
rs752417906	snp	A/C/T	9.29349e-05	0.00681615	intron-variant	MYCBP2	GRCh38.p7	13:77156237	AATAAACAAAACCCC[A/C/T]AACACTGATCAGCAT	23077
rs752423916	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77070276	GCGAGCATAAAAAAG[A/C]CTTCATAAATTTTTC	23077
rs752437455	snp	C/T	1.65113e-05	0.00287322	missense	MYCBP2	GRCh38.p7	13:77260556	ATCTTAATTATCTTT[C/T]TAGGTTTATAAGGTT	23077
rs752463227	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77093388	ATACAGATCCTCTCC[A/G]TTTTTAATCTCTTTC	23077
rs752470906	snp	C/T	1.65296e-05	0.00287481	missense	MYCBP2	GRCh38.p7	13:77181760	GAACTAGTGTTGAGT[C/T]GTTCTCTGTACTAAC	23077
rs752478616	in-del	-/AGG	1.67539e-05	0.00289425	cds-indel	MYCBP2	GRCh38.p7	13:77191775	CACCACCCAGCTTGC[-/AGG]AGAACAGGCTCATCA	23077
rs752482473	snp	C/T	3.30486e-05	0.00406487	missense	MYCBP2	GRCh38.p7	13:77096316	GAATAAAATACCTTC[C/T]CCCTTGCAGCAGCCT	23077
rs752490482	snp	A/G			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77227659	TGTTCATATGATTCT[A/G]CCAGACTTAATTAAA	23077
rs752490900	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77120915	GATTACTGGGTTAGA[A/G]ATTCAAAACCACATA	23077
rs752491991	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77274677	ATGGATAACTCCACT[G/T]TTCCCTATCTCATCA	23077
rs752492473	snp	A/C	3.30278e-05	0.0040636	intron-variant	MYCBP2	GRCh38.p7	13:77261123	TTTTATTTTTACTAA[A/C]ATAAAGCATTTATTT	23077
rs752494810	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77137598	TCTCTATATTTTTGT[G/T]TTTTTTTTGAGACAG	23077
rs752502490	snp	A/G	1.70443e-05	0.00291923	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77083230	TTTATCAGTTTGTGT[A/G]CTGGAAGGAATCCTC	23077
rs752506341	snp	A/G	1.69686e-05	0.00291273	intron-variant	MYCBP2	GRCh38.p7	13:77058415	CGTATTCCTGTTAAA[A/G]ATGAATTACAATGTT	23077
rs752507966	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77324078	CTCAACTTTGAAATC[C/T]CCTTGAGTTACCAAA	23077
rs752525686	snp	A/C	1.64773e-05	0.00287026	missense	MYCBP2	GRCh38.p7	13:77139247	ATTAAAAGAGAGGCA[A/C]CAGGCTTCAGTGTAA	23077
rs752530227	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77050050	AATATTAGCCACTAC[C/T]CTACTGGACACTAGC	23077
rs752534075	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77057920	TCAGATCACTGCAAG[C/T]TCCGTCTCCTGGCTT	23077
rs752534640	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77290420	AGTACACGAATGTTC[A/G]TAATAGCATTCTTTT	23077
rs752541241	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77071914	CTGAACCAGAAATTA[A/G]TAATATAAAGCTAAC	23077
rs752541443	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77155639	ATATATTTCTAACTT[A/C]ATGAGTGTTATTTTT	23077
rs752542307	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77055068	GAGGTCACCCAAGGT[A/G]AGGAAGTATTTATTA	23077
rs752577066	snp	C/T	1.70458e-05	0.00291935	intron-variant	MYCBP2	GRCh38.p7	13:77140004	AAACAATGCAAAAAC[C/T]TTCTGTCCAAAATTT	23077
rs752585186	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77264098	ATGAGAGTTCTCCAC[A/G]CAATAAGGATAAACT	23077
rs752591919	in-del	-/T			intron-variant	MYCBP2	GRCh38.p7	13:77316941	CCAAATGGTGACTTC[-/T]TTTTTTTGTTGTTTT	23077
rs752617535	in-del	-/C			intron-variant	MYCBP2	GRCh38.p7	13:77050863	TAAGCTTACAAGGAT[-/C]AAGGAATTCCTCCTG	23077
rs752619042	in-del	-/AAC	0.226843	0.248925	intron-variant	MYCBP2	GRCh38.p7	13:77243178	AGATGATTGGCCAAA[-/AAC]AACAACAACAACAAC	23077
rs752623493	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77302445	AGTAACCTGGAATCA[C/T]GTAACCTTTAAGAAT	23077
rs752627023	snp	A/G	5.3445e-05	0.0051691	intron-variant	MYCBP2	GRCh38.p7	13:77166604	TATATATATACACAA[A/G]CATACACATCTGCAT	23077
rs752634142	snp	A/G	6.59087e-05	0.00574021	missense	MYCBP2	GRCh38.p7	13:77067611	ATCGGAAGAGTAACT[A/G]TTGTAACTCCTTTGC	23077
rs752666301	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77241235	AAGTTATCAATGCAC[A/G]ATTCAATGTTCCTTT	23077
rs752668972	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77134227	ATAAAACTGGAAAGC[A/G]TGTTCTCAGCCGGGT	23077
rs752679168	snp	A/G	1.64849e-05	0.00287092	missense	MYCBP2	GRCh38.p7	13:77212063	CTTGCACCTATCCAA[A/G]TAGCTTTTCTTCCAT	23077
rs752684069	snp	C/T	1.65364e-05	0.0028754	missense	MYCBP2	GRCh38.p7	13:77156131	GTGGTAGGCCAACCA[C/T]AACGAATATCATCCT	23077
rs752684981	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77135147	AGAGATAGACACAAA[C/T]AGTGCTGAAGGCAAC	23077
rs752685651	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77317018	GCAGTGGCGCAATCT[C/T]GGCTCACTGCAACCT	23077
rs752686944	snp	C/T	3.2994e-05	0.00406152	missense	MYCBP2	GRCh38.p7	13:77165335	AACCATAGAAAGAAG[C/T]TTTGTCATCTTTCAC	23077
rs752692386	snp	C/T			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77292035	GCTTTACAATGTGTA[C/T]CTGAGTTTCACTTAC	23077
rs752698187	snp	A/G	1.64806e-05	0.00287054	synonymous-codon	MYCBP2	GRCh38.p7	13:77062653	GGAGAGACGATCTAC[A/G]TGGTCCTGATCAAGA	23077
rs752705459	in-del	-/ATAA			downstream-variant-500B	MYCBP2	GRCh38.p7	13:77044360	GTAAGACCCTGTCTC[-/ATAA]ATAAATAAATAAAGT	23077
rs752706839	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77187580	TTAGAATAATGGTAC[A/G]CAAACGGAGAAGACT	23077
rs752710125	snp	G/T			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075674	TTGTTGATTTCTTTT[G/T]GGGGGGGGTGAGGGG	23077
rs752725408	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77125264	TCTTTAAAACAAAAG[A/C]AATACAATAGGCATT	23077
rs752726861	snp	A/G	1.65113e-05	0.00287322	missense	MYCBP2	GRCh38.p7	13:77098488	CCTCTCAAAGGTTCT[A/G]TGAGGGGCATTTTCT	23077
rs752734200	snp	A/G	1.66654e-05	0.00288659	synonymous-codon	MYCBP2	GRCh38.p7	13:77191756	TCGGGCCCATGCCAC[A/G]TACCACCACCCAGCT	23077
rs752739048	snp	C/T	1.66432e-05	0.00288467	missense	MYCBP2	GRCh38.p7	13:77206790	TCAGCAACCACCGCA[C/T]TGTAACACCACAGCT	23077
rs752739425	snp	A/G			intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77325786	TGCAACCTCATTTCT[A/G]GAAGACCAAAAGGCC	23077
rs752748046	snp	A/G	3.30142e-05	0.00406276	synonymous-codon	MYCBP2	GRCh38.p7	13:77165363	CACATAATCTGATGC[A/G]GTCTCCAATGAAAAA	23077
rs752762644	snp	C/T	1.6566e-05	0.00287797	intron-variant	MYCBP2	GRCh38.p7	13:77288153	ATTAATAGAACTCAG[C/T]GGCTTACCTTTGGAA	23077
rs752766217	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77266841	CCGCTTTCCAAAGCT[C/G]CTCTATTTCTGAAAT	23077
rs752795985	snp	A/G	5.06727e-05	0.00503327	utr-variant-3-prime	MYCBP2	GRCh38.p7	13:77045344	TGGGGGATGAAGGCA[A/G]TTTTTCTCTCTGTAG	23077
rs752800251	snp	A/T	1.64879e-05	0.00287118	missense	MYCBP2	GRCh38.p7	13:77171578	CTGCTACAGTTTTTA[A/T]CTTCTTCATTGGCTT	23077
rs752800708	snp	A/G	1.64961e-05	0.00287189	missense, nc-transcript-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77076821	TCTGGTGTAGGTTCA[A/G]CATCTCCAGAGATGA	23077
rs752802643	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77216287	AACAGGAAAGGAGGG[C/G]TCTTGCTTAGAGTAA	23077
rs752805997	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77232211	GACTATGACAATTTT[A/G]CAGCAAAAAAAAGAA	23077
rs752806070	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77172930	GTCTCAGTTCCATCA[G/T]CTGTGAAACAGGGAT	23077
rs752811010	snp	C/G			intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075201	TGACAGAGAGAGACC[C/G]GGTCTCAAGCAAAAC	23077
rs752820388	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77279772	GGAAATATGAAGGTA[C/T]ACTAGACCCTGTCCT	23077
rs752821319	snp	A/G	1.65625e-05	0.00287766	synonymous-codon	MYCBP2	GRCh38.p7	13:77097959	ACTCCTTATAGGAGC[A/G]TGTTCTTTGGAAAGT	23077
rs752823602	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77268313	AAAATGAATAGCATA[C/G]TGGTTTCAGAAGGTG	23077
rs752840666	snp	C/G	3.30945e-05	0.0040677	missense	MYCBP2	GRCh38.p7	13:77098102	TGGCTTGCTTGGCTG[C/G]CTCTAAAGGCTTGGA	23077
rs752841648	snp	A/G	1.68621e-05	0.00290358	missense	MYCBP2	GRCh38.p7	13:77186036	TCCAGCTCCAGTGAA[A/G]AATACTCAACAATGA	23077
rs752859891	snp	A/G			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77293644	CAATGTAATCACAAG[A/G]GTCCTTACAAGTGAA	23077
rs752863753	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77279636	TTAGTAGAAACTCCC[-/A]AAAACCATTAATTCT	23077
rs752873413	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77159675	TCTCTCTCTCCTGCT[A/G]CCATGTAAGACTTGC	23077
rs752885629	snp	A/G/T	3.32941e-05	0.00407997	intron-variant	MYCBP2	GRCh38.p7	13:77263920	CTACTTAAGATTCAG[A/G/T]ATACTTACATCTCTT	23077
rs752888680	snp	A/G	1.92565e-05	0.00310288	missense	MYCBP2	GRCh38.p7	13:77064643	ATACATCTCACTGGA[A/G]ACCTAAATTCTTCTT	23077
rs752903228	snp	C/G	1.65029e-05	0.00287248	intron-variant	MYCBP2	GRCh38.p7	13:77233110	TTCAAATGAGTGGAA[C/G]AAATTGGGAAAGTAT	23077
rs752909159	snp	A/T	3.32502e-05	0.00407725	missense	MYCBP2	GRCh38.p7	13:77181835	TCGGGAAGATGGAAG[A/T]CAGCTTAACAGACGT	23077
rs752916941	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77105807	TCAGGATTTTTCTCC[A/C]GTGCTCATTTGAAGT	23077
rs752921908	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77124429	ATGCATGTTCTCTTA[C/T]TTACCTAACTTCATC	23077
rs752927415	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77296000	AGTTTCTAGTACCTG[C/T]AGTCAGATTGAAAAA	23077
rs752930444	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77230591	TTCATTGATATTTCA[C/T]ATACAAATTACTCAC	23077
rs752933201	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77258504	ATTAAAATAAAAACA[C/T]GTTATCAAGTATTTG	23077
rs752964278	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77059467	TTTTCTGTATGAAGT[A/G]AAGGTGTCACAGGGG	23077
rs752970171	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77140324	AATAACAGTATAACA[A/C]CACTAACAACAGAAC	23077
rs752974489	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77280779	GTTTTAGTGAGACTG[C/G]CCCATAAAACTTTGG	23077
rs752986080	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77295016	AGTATAAGAGATTGC[C/T]TCTTGCTCAGAGCAA	23077
rs752993716	snp	C/T	1.66449e-05	0.00288482	missense, utr-variant-5-prime	MYCBP2	GRCh38.p7	13:77278871	GAAAATCGTGTCTCT[C/T]TGATCAATTCAAAAA	23077
rs752996730	snp	C/T	5.35949e-05	0.00517635	intron-variant	MYCBP2	GRCh38.p7	13:77174513	TAAAGATGTAAAACA[C/T]CTTTTATTCACAATG	23077
rs753000758	snp	A/G	3.3071e-05	0.00406625	synonymous-codon	MYCBP2	GRCh38.p7	13:77206687	ATGAGATCGGGTAGT[A/G]AGGGCCCTTGATCCT	23077
rs753018973	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77128144	ACATGAATACACAGA[C/G]AGCACTCAAGATAAA	23077
rs753035832	in-del	-/TG			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228694	AAGATGAATATGTTG[-/TG]TGTGTGTGTGTGTGT	23077
rs753036183	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77208591	CTCTAAATTATTTTT[G/T]AGCAAAAAATCTAAC	23077
rs753038340	snp	A/G	1.76683e-05	0.00297218	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081686	GTACTTATGATACTT[A/G]AAAGCAAATCTTTCG	23077
rs753047398	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77152533	TGTTGCCTTTTTGGC[C/T]AGCCCTGCCCCCCTA	23077
rs753056877	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77066273	AGCAGTTAAGGTTAT[C/T]TGAGTTCCCTTTCAA	23077
rs753069824	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77188587	TATGCAACTCTTCCA[C/T]CTAGTTCCTCAAGTA	23077
rs753113015	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77113766	CTGAGAAGATGGCTC[A/G]GCTCAGTGAAGATAA	23077
rs753119277	snp	A/C	0.0869962	0.189552	intron-variant	MYCBP2	GRCh38.p7	13:77217965	GACATCCCCTAGGTT[A/C]AAAAAAAAAAAAGTA	23077
rs753125388	in-del	-/AC			intron-variant	MYCBP2	GRCh38.p7	13:77258325	CTTCCACAATCCAAT[-/AC]ACAGTTATTTTCTAA	23077
rs753126196	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77209930	TACCACATGGCCTCT[A/T]AGAACTTGGCTGTCT	23077
rs753131651	snp	A/G	0.0287556	0.116408	synonymous-codon	MYCBP2	GRCh38.p7	13:77098676	CCTATTGGCTGGGAG[A/G]GTCTTTGGCTTAGGA	23077
rs753136939	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77088356	ATAATTCCCATCCAT[G/T]AAGTGGTAGGTTATT	23077
rs753141378	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77072536	ATACAAGGCAAACAT[-/A]GGGAAAGAAATAAAG	23077
rs753155953	snp	A/T	1.64732e-05	0.0028699	missense	MYCBP2	GRCh38.p7	13:77125416	TCACTCTCACAGAAC[A/T]CTACCATGCTGTTCT	23077
rs753156407	in-del	-/C			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087061	TTGTTAGTTCTTGCT[-/C]ATGGTGTCTTGTTTG	23077
rs753157329	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77310469	ATATATTGTCTGTGG[C/T]TGCTTTCAAACTAAA	23077
rs753162776	snp	C/T	1.76696e-05	0.00297228	intron-variant	MYCBP2	GRCh38.p7	13:77146268	TCATTTAAAAACATT[C/T]TCAATTAACAGAGTA	23077
rs753166122	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77273261	AAAGATTTAAGAGGT[C/T]TGGCCAAAATTCATT	23077
rs753184744	snp	C/T			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77078442	GTGTTATAAGTGTTA[C/T]AACAGACAGATTTTT	23077
rs753188176	snp	A/G			utr-variant-3-prime	MYCBP2	GRCh38.p7	13:77044967	TTTTTATCCCCACCC[A/G]TGATGCAATTGTACA	23077
rs753194778	in-del	-/A	5.00722e-05	0.00500336	intron-variant	MYCBP2	GRCh38.p7	13:77169599	CATTCAAAGTTATAG[-/A]ATTAAATTACACACC	23077
rs753199881	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77231050	TGAGCAGTAAATTAA[C/T]ACTCTTCACAAAAAA	23077
rs753223850	in-del	-/ATT			intron-variant	MYCBP2	GRCh38.p7	13:77155523	AATATGCTCTGAAAC[-/ATT]ATTATTAATATTTCA	23077
rs753227566	snp	A/T			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081219	GGTATATTTGTAATC[A/T]GACCTCTTTTCAGAA	23077
rs753235380	snp	A/T	7.25597e-05	0.00602284	intron-variant	MYCBP2	GRCh38.p7	13:77262034	AATGCTCATTTTTAA[A/T]CCAAAGAGAATAATT	23077
rs753242183	in-del	-/T	1.65211e-05	0.00287407	intron-variant	MYCBP2	GRCh38.p7	13:77161893	TTTATCCTTAAAACA[-/T]TTGGGACAATACCTG	23077
rs753268843	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77257067	TAAAAAACACTGAGA[G/T]CCTATCATTTGCAAC	23077
rs753270474	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77221481	CTTCTGAGTGCCAAG[C/T]GCACAGTAAGATAAC	23077
rs753274654	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77151024	ATAAGCAACTTACTA[C/T]TATAAACTCATAATT	23077
rs753280095	in-del	-/TATTC			intron-variant	MYCBP2	GRCh38.p7	13:77048525	CTGTGGGATCTCCTT[-/TATTC]TATTCCAGTTCTCTA	23077
rs753292229	snp	C/T	4.99247e-05	0.00499598	missense	MYCBP2	GRCh38.p7	13:77057056	TTTTCTAATACTCGC[C/T]GACAGCACTGTAAGT	23077
rs753293749	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77132024	AAAATGATGAAATGA[C/T]TCAGGAAAATTAAGA	23077
rs753294626	snp	C/T	3.3006e-05	0.00406226	missense, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77077249	TTTTTGTGCTTTCAC[C/T]ATCTTTCCAGCCCAG	23077
rs753305484	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77115021	TCATATTGTCACAGT[A/G]TAGTTGGCTTTAATT	23077
rs753316874	snp	A/C	3.30458e-05	0.0040647	synonymous-codon	MYCBP2	GRCh38.p7	13:77061263	ACCACAACCTTCATG[A/C]AGGTCAACCTTTATA	23077
rs753318298	snp	C/T	1.80208e-05	0.00300168	intron-variant	MYCBP2	GRCh38.p7	13:77180095	AACTTACACATGTGC[C/T]TTTTATCCAGTGTCA	23077
rs753319419	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77066395	TAATGTGGAGCTTAA[C/T]CGGAATATAAATTCA	23077
rs753321599	snp	A/G	1.72791e-05	0.00293926	intron-variant	MYCBP2	GRCh38.p7	13:77174499	ATTTTCCTTCATTAT[A/G]AAGATGTAAAACATC	23077
rs753326412	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77307169	CAAATCTGAAACTTC[C/T]TCCTTCCCCCATCCC	23077
rs753342811	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77238512	ACTTAAGAATTTCAC[C/T]GAATAAGCACTTCAC	23077
rs753352467	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77302851	AAAAGGGTCAAATCA[A/T]TAGGAAATCATAACA	23077
rs753360647	snp	C/T	1.64833e-05	0.00287078	synonymous-codon	MYCBP2	GRCh38.p7	13:77051019	ACAGTGTGGTAGTTC[C/T]TCCTTAGGAATGCTA	23077
rs753371336	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77307498	AGGCACGGTGGCATG[G/T]GCCTGTAGTCCCAGC	23077
rs753373972	snp	A/T	1.64727e-05	0.00286986	stop-gained	MYCBP2	GRCh38.p7	13:77185241	CAAGGGTTGACTGAG[A/T]TATCCTTGAGGATCA	23077
rs753378191	snp	A/C/G	6.04337e-05	0.00549671	intron-variant, missense	MYCBP2	GRCh38.p7	13:77118402	GGGCTGTGTACTAGG[A/C/G]AAGAGGGAGGTTTTG	23077
rs753378714	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77118594	CAGATAGAGTTGAAC[A/G]CTAAATAAAACCATG	23077
rs753388461	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77258780	ACATGCTTTGAGACC[C/T]TACATGATGTGCTAA	23077
rs753393249	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77222538	GACCCTGCCTCAGCT[C/T]GAAGGGTAGAGAGTG	23077
rs753400265	snp	C/T	1.64779e-05	0.00287031	synonymous-codon	MYCBP2	GRCh38.p7	13:77243075	TCTTCCTTCCTCTAA[C/T]CTGTGCCTTCTGATT	23077
rs753415800	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77165757	CCTGGAGTGTGGCTT[C/T]TTCTGATCTTTTCCC	23077
rs753428552	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77198838	GCCTCCTCTGTCATT[A/T]AAATGGCTATAAGAA	23077
rs753429848	in-del	-/AA	0.0240504	0.10699	intron-variant	MYCBP2	GRCh38.p7	13:77070728	TTTACATAGAAAAAG[-/AA]AAAAAAAAAAAAGAA	23077
rs753441299	snp	C/T	1.66896e-05	0.00288869	intron-variant	MYCBP2	GRCh38.p7	13:77068853	AAAGTTAACACAGAA[C/T]ATGTAAAAATATAGG	23077
rs753468603	snp	A/T	1.92402e-05	0.00310157	intron-variant	MYCBP2	GRCh38.p7	13:77181941	TTAAAAACAAAAATA[A/T]GGCCCCCCAACCAAA	23077
rs753481534	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77045561	TATAAACCTCACAGA[A/T]ATATAAATCACTGAT	23077
rs753482142	snp	C/G	1.64955e-05	0.00287184	missense	MYCBP2	GRCh38.p7	13:77205309	GACCAAGACCACCAA[C/G]TAAAATATCAGTGTC	23077
rs753489488	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77285955	GGTACAGTTAGGACA[C/T]TGCAGACAAAGGAAA	23077
rs753490246	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77145931	TATCTACTTTACATA[C/T]CTATTTTCACTAGTA	23077
rs753492849	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77321555	TGGTCTTCAAGATGC[C/G]CCATCCTAGCCAAAG	23077
rs753513375	snp	C/T	1.99372e-05	0.00315725	splice-donor-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326473	CACCCTGGGGACGCA[C/T]CTGGAGGCTGGGTGT	23077
rs753535447	snp	A/G	3.31873e-05	0.0040734	intron-variant	MYCBP2	GRCh38.p7	13:77205427	TTAAAAGATCCATAT[A/G]TATTTCAGTTGTAAG	23077
rs753549051	in-del	-/TTTTTTTTTGTTTT			intron-variant	MYCBP2	GRCh38.p7	13:77311556	GCAGGGAAAGAGAAG[-/TTTTTTTTTGTTTT]TTTTTTTTTGTTTTT	23077
rs753552265	snp	C/T	5.34764e-05	0.00517062	intron-variant	MYCBP2	GRCh38.p7	13:77166597	ATACAGATATATATA[C/T]ACACAAACATACACA	23077
rs753565918	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77122332	AACCTTATGAAAAAT[-/A]AAAATATCTCAAGTA	23077
rs753570014	snp	C/T			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77080339	AATATGCAAATGGCA[C/T]AGGAGAAGCCAGGCA	23077
rs753576516	in-del	-/TTGC	2.20953e-05	0.00332373	frameshift-variant, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77087500	TGTTCTGAATTTTCT[-/TTGC]TTGTTTTATTTTCTT	23077
rs753583464	snp	C/T	5.21399e-05	0.00510561	intron-variant	MYCBP2	GRCh38.p7	13:77257848	TAGGAAAGAAACAAA[C/T]TTAGTAAAAACAACA	23077
rs753588338	snp	C/T	1.66197e-05	0.00288263	missense	MYCBP2	GRCh38.p7	13:77097454	TATCTTTCTCTGGTC[C/T]TCCTACTGCCAGCTG	23077
rs753604782	in-del	-/A/AA/AAA/AAAA	0.0173476	0.0916533	intron-variant	MYCBP2	GRCh38.p7	13:77243959	ACAGATCCTAGGGGG[-/A/AA/AAA/AAAA]AAATACAAAAAAAAA	23077
rs753615543	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77073240	ATATATGGATTATCT[C/T]ACGGAATAAAAGAAA	23077
rs753624906	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77108970	AGTGCTGGGATTACA[A/G]GCATGAGCCACTGTG	23077
rs753627742	snp	A/G	3.30442e-05	0.0040646	synonymous-codon	MYCBP2	GRCh38.p7	13:77098364	GACTTCGACCACCTC[A/G]CTGTGGAGGTTTTCC	23077
rs753646677	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77300502	TAAAAACCACTTTTA[C/G]TTCACAGGCTACATA	23077
rs753666559	snp	G/T	1.68312e-05	0.00290092	intron-variant	MYCBP2	GRCh38.p7	13:77150992	ACCATTATTATTTAA[G/T]TGTCACTGACATCAA	23077
rs753667196	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77265516	ATAAAAAAAGTATGT[C/T]TTAAGTTCATCAAAA	23077
rs753671923	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77144028	GATTAACACAATGAT[C/T]GATTTAAAAATGCAT	23077
rs753672022	in-del	-/T			intron-variant	MYCBP2	GRCh38.p7	13:77173186	CTTTAACATTTTTCA[-/T]TTATAAAAAATGTAA	23077
rs753685357	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77248948	CAAAAAGCAAAGATG[C/T]TCCGACATATGTGAC	23077
rs753691998	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77094677	ATTCTTCCAAGAGTC[A/G]CTTTCTTCCTGTCGC	23077
rs753693008	in-del	-/ATCCTGGCTAAA			intron-variant	MYCBP2	GRCh38.p7	13:77169210	CAGGAGATCGAGACC[-/ATCCTGGCTAAA]ACGGTGAAACCCCGT	23077
rs753694479	snp	A/C	3.35121e-05	0.00409328	intron-variant	MYCBP2	GRCh38.p7	13:77270113	TTCATAATTAATAAT[A/C]AATGAAAAATAATAC	23077
rs753703915	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77157845	CCAGACTTTTTTAAA[A/G]TAGTATTTTAATATT	23077
rs753711836	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77109729	AAAGTCAGAGATCCT[A/G]AATGGAGGGACTGGC	23077
rs753728443	snp	A/G			intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77291548	GGCCAAGGCGGGCAG[A/G]TCACCTGAGGTCAGG	23077
rs753735835	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77264197	ATTACATTTTTGCTT[A/C]TATTTATAAATCTTC	23077
rs753749692	snp	C/T	2.28022e-05	0.00337647	intron-variant	MYCBP2	GRCh38.p7	13:77288428	TTTTCTATCATCAAG[C/T]CCCATTTTACATAAA	23077
rs753755288	snp	C/T	3.30797e-05	0.00406679	missense	MYCBP2	GRCh38.p7	13:77176511	CCTTTAAAGGAACCA[C/T]TTTGTCAAGTCTGAT	23077
rs753759836	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77244374	TTGGTAGCCTTCAGC[A/G]ACAGAGCCTAAGCTT	23077
rs753760871	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77058065	CAGGATGGTCTCGAT[A/C]TCCTGACCTCGTGAT	23077
rs753761207	snp	A/G	1.66236e-05	0.00288297	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77077401	ACCTGGTTGAGTAGA[A/G]AAGAGGCAGGAACCT	23077
rs753764804	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77188199	CTTTTATCTCATTCC[C/T]ACCAGGAATATATAT	23077
rs753773214	snp	C/T			upstream-variant-2KB, nc-transcript-variant	MYCBP2, LOC107984564	GRCh38.p7	13:77327600	GGTAGTAATCTAGCA[C/T]ATTCTTTTTTGTGTG	23077
rs753778407	in-del	-/G			intron-variant	MYCBP2	GRCh38.p7	13:77154594	AGAAATATCAGAAGC[-/G]TAACAGTATGAACAT	23077
rs753810487	snp	A/G	1.65449e-05	0.00287614	intron-variant	MYCBP2	GRCh38.p7	13:77243198	CAACAACAACAACAT[A/G]TATGTTATATAATAG	23077
rs753812427	snp	A/G	1.65002e-05	0.00287225	synonymous-codon	MYCBP2	GRCh38.p7	13:77211238	TTGTTCTGAGTCATT[A/G]AAAGTTTTACAACTC	23077
rs753813040	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77072071	AGGTGGGTGGATCAC[A/G]AGGTCAGGAGATCGA	23077
rs753815855	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77262764	TATGAGTAATTGTAG[C/T]TTTACATATGGTACA	23077
rs753823296	snp	A/G	0.000120175	0.0077507	intron-variant	MYCBP2	GRCh38.p7	13:77118529	TCAAAACTACAACTC[A/G]TTATTCATTAACATC	23077
rs753823359	snp	A/C	1.6495e-05	0.0028718	missense	MYCBP2	GRCh38.p7	13:77098271	TTTATTTGAACCTTC[A/C]TCCACACTCTTAAAT	23077
rs753833756	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77172441	AAGCTGGGTTTGGAG[C/T]AAGGGTGGAACTTGG	23077
rs753840677	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77304650	TGATAAATGTCGGAG[G/T]TGATAAATATGCTAA	23077
rs753847940	in-del	-/A	6.69378e-05	0.00578484	intron-variant	MYCBP2	GRCh38.p7	13:77169717	GGAATGTCATCAGCT[-/A]AAAAAAGGCATAAAA	23077
rs753852122	snp	A/C	1.84283e-05	0.00303542	intron-variant	MYCBP2	GRCh38.p7	13:77189094	TAGAAAGTCCAATGT[A/C]ATTTTTTCTTTTTAA	23077
rs753852989	in-del	-/AA			intron-variant	MYCBP2	GRCh38.p7	13:77153680	CAAACTGTGTTACTT[-/AA]AAAAAAAAAGTTATT	23077
rs753860888	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77270202	TTACACTAAAATTAG[A/G]TCATATTCTAGAAAT	23077
rs753867367	snp	C/T	0.000170692	0.00923672	intron-variant	MYCBP2	GRCh38.p7	13:77211342	AAAAAAATATTTATA[C/T]ATAATTTTAATATAT	23077
rs753883110	snp	C/T	1.64849e-05	0.00287092	synonymous-codon	MYCBP2	GRCh38.p7	13:77166465	AGTTCTGACAGGAAT[C/T]AACAAACGAAGGACA	23077
rs753885219	snp	A/G	1.65083e-05	0.00287296	intron-variant	MYCBP2	GRCh38.p7	13:77278707	GTACAATACTCTATT[A/G]TTAATTATATTCACT	23077
rs753889266	snp	A/G	1.64923e-05	0.00287156	missense	MYCBP2	GRCh38.p7	13:77098899	TTCTTCTGATCAGCA[A/G]TAGTCCGGCTCATAC	23077
rs753896083	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77313878	TCACCGAACAAGATA[C/T]ATAGATGGCAAATAA	23077
rs753899993	snp	A/G/T	4.98459e-05	0.00499204	intron-variant	MYCBP2	GRCh38.p7	13:77161972	TGTTGTGTAAATAAA[A/G/T]AGTTTTACTAAAATA	23077
rs753911552	snp	C/G	1.65004e-05	0.00287227	missense, utr-variant-5-prime	MYCBP2	GRCh38.p7	13:77225455	TGGTGAAATCCACAG[C/G]TGACTTGGACTGCCC	23077
rs753934013	snp	G/T	1.69009e-05	0.00290692	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77083214	CAGAAATTGAAACAA[G/T]TTTATCAGTTTGTGT	23077
rs753942460	snp	C/G	3.4246e-05	0.00413785	intron-variant	MYCBP2	GRCh38.p7	13:77181650	AGGCAATAAATAAAA[C/G]CATTTAGAGTTTTAG	23077
rs753944185	snp	C/T	4.94817e-05	0.00497377	missense	MYCBP2	GRCh38.p7	13:77070711	CAGCATCTGATGTTG[C/T]CTTTACATAGAAAAA	23077
rs753944392	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77198064	ATCCTCCTGATGAGC[C/T]TATTAGACATTGTCA	23077
rs753964846	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77234115	TAAAATAAAATAAAT[C/T]ATTTTTCCCATTAAC	23077
rs753965004	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77048849	TCAGCTACTACCCAC[C/G]ACTGAGTTCTCTAAA	23077
rs753968111	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77159159	ATCCTGGCTTTGGAC[A/C]AATTATTTGCTGTGT	23077
rs753972352	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77063167	ATAAAAGTTCCTCAG[A/C]AGTCTTTGTTGCCCC	23077
rs753974026	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77220408	CTGGCCAAGATCATA[C/T]AGCTACCAAGTGACA	23077
rs753975405	snp	C/T	1.65056e-05	0.00287272	missense	MYCBP2	GRCh38.p7	13:77097796	TAAGCATAGACAATA[C/T]CTTGTTTTTGTTGAT	23077
rs753978457	snp	A/G	1.73685e-05	0.00294685	intron-variant	MYCBP2	GRCh38.p7	13:77205601	GTATCAAGACAACCT[A/G]AAACAACAAAGAAAC	23077
rs753984831	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77168351	CTTGTAAATACAGGC[C/G]AGGCATTCTTTAAGA	23077
rs753988944	snp	A/G	3.30376e-05	0.0040642	synonymous-codon	MYCBP2	GRCh38.p7	13:77176560	TGAGTCATCCGTTGT[A/G]TACGTTCCTTTCACT	23077
rs753992403	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77147670	AAGGCTGAGTCTTTA[C/G]CCATACAAAGGTGAG	23077
rs753992492	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77266209	ACCCATGTGTTATAG[C/T]GGATGGGATGTGTCA	23077
rs753994233	in-del	-/A			intron-variant	MYCBP2	GRCh38.p7	13:77210608	CCTGTATATTTCTCT[-/A]CCAGTAAGAGTATTT	23077
rs754003928	snp	A/G	1.67396e-05	0.00289301	missense	MYCBP2	GRCh38.p7	13:77058399	CTACAGGCTATCTTA[A/G]CGTATTCCTGTTAAA	23077
rs754005885	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77317153	AACAGGGTCTCACCA[C/T]GTTGGCTGAGCTGGT	23077
rs754017235	in-del	-/G			intron-variant	MYCBP2	GRCh38.p7	13:77220297	GGGCATAAAGTCAAA[-/G]GGAAATAAAGTAGGG	23077
rs754034246	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77198819	AATGTCCCTAAACAG[C/T]TGTGCCTCCTCTGTC	23077
rs754049581	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77233645	TTCGTTGAAGACAGA[C/T]ATCTTTTCCATTGAA	23077
rs754057482	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77187089	TGCTGGGATTATAGG[C/T]GTGAGCCAATGTGCT	23077
rs754062436	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77188417	ACATACGTAAGAATC[A/C]TCAATTAATACATGA	23077
rs754064048	snp	A/G	3.30126e-05	0.00406266	missense	MYCBP2	GRCh38.p7	13:77260526	CAGGCTGTATATACC[A/G]CAATCTTTCCTTCCA	23077
rs754069015	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77218455	CAGTATCATGAGAGG[C/T]ATTAGAGCAGTGACT	23077
rs754071228	snp	A/G	1.65304e-05	0.00287488	synonymous-codon	MYCBP2	GRCh38.p7	13:77156127	TATGGTGGTAGGCCA[A/G]CCACAACGAATATCA	23077
rs754073175	snp	C/T	3.31472e-05	0.00407093	synonymous-codon, intron-variant	MYCBP2	GRCh38.p7	13:77126477	ATCTTGTTCTTGCAT[C/T]GTTGCTTCCTGTGGG	23077
rs754083684	in-del	-/TTAA	1.70307e-05	0.00291806	intron-variant	MYCBP2	GRCh38.p7	13:77162007	AATATTTAGTTTAGT[-/TTAA]TTTTCTAGTCCTTTG	23077
rs754092836	snp	C/T	0.00019916	0.009977	intron-variant	MYCBP2	GRCh38.p7	13:77121531	GTAACATTAGTTTCT[C/T]ACGTGCTATTCCCTA	23077
rs754096869	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77105383	GATTCCTAGGTATGA[C/T]TCAGAGTGAAAAAAA	23077
rs754104401	snp	C/T			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77078971	ATGACCTACTAATAC[C/T]ACATCAACTCTTCTG	23077
rs754109900	in-del	-/T			downstream-variant-500B	MYCBP2	GRCh38.p7	13:77044610	CTGGACTTTTAGACC[-/T]TAAAGGTGTTCAAAT	23077
rs754111424	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77140572	TGACAGTAGAGGACA[C/T]TTTCACCTTGCAAAC	23077
rs754115266	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77313458	AATCTAGAAACAAAC[C/T]TTACACCCTTCACAA	23077
rs754116808	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77161169	ATTTGACAAATGCTG[A/T]CTACAGATTCTGATA	23077
rs754119544	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77210743	ATAGAATGAATTCTA[C/T]ACAATATAAACAGGA	23077
rs754120634	snp	A/T	1.64966e-05	0.00287194	intron-variant	MYCBP2	GRCh38.p7	13:77171482	ACTACTGAGAAAGAA[A/T]AAATATTACCATCCA	23077
rs754126142	snp	A/G	1.6489e-05	0.00287128	missense	MYCBP2	GRCh38.p7	13:77139204	TACTTACGTCAACAG[A/G]GACCAGAAGACTCTT	23077
rs754126625	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77318274	ATGAAAACCCTTTTA[C/T]TGGGCCCATGCACAG	23077
rs754135967	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77101173	CACATAATGGGAATC[C/T]AGACAAACAATTAGT	23077
rs754143809	snp	C/G	1.65337e-05	0.00287517	synonymous-codon	MYCBP2	GRCh38.p7	13:77181734	ATGTGCCACCAAAAG[C/G]GGAAAACGATGAACT	23077
rs754153708	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77126954	GGTAAAAAAAAGTCT[A/G]AATATTCATTTCTTC	23077
rs754164388	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77232426	AATTCCTTGTATTAA[A/G]TTCTTTCCTGATCTT	23077
rs754165692	snp	A/G	2.01908e-05	0.00317726	intron-variant	MYCBP2	GRCh38.p7	13:77243955	CAACCACAGATCCTA[A/G]GGGGAAATACAAAAA	23077
rs754178171	snp	A/T	1.66576e-05	0.00288592	intron-variant	MYCBP2	GRCh38.p7	13:77263907	CCATTTACACTAGCT[A/T]CTTAAGATTCAGGAT	23077
rs754190433	in-del	-/CAAT			intron-variant	MYCBP2	GRCh38.p7	13:77207228	TATAAGAGCTAGAAA[-/CAAT]CAATCCATAGCAAAA	23077
rs754192300	snp	A/C/G	5.14499e-05	0.00507176	intron-variant	MYCBP2	GRCh38.p7	13:77090315	AGAGCTGAATGAAAT[A/C/G]TAACTATACTTATAA	23077
rs754193239	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77267444	AAAATTAAATTAAAT[A/T]AAATAAGGAGGAAAA	23077
rs754197897	in-del	-/CGCCGCCGCCGC			cds-indel, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326779	GCACATCATCATCCT[-/CGCCGCCGCCGC]CGCCGCCGCCGCCTC	23077
rs754200051	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77053806	TTTTTGCTACATTGG[A/G]AGACTATGCACCTTT	23077
rs754210285	snp	A/G	1.64838e-05	0.00287083	synonymous-codon, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081496	TTTTACACAGTTGAT[A/G]GTGATGTTCTTAGTT	23077
rs754219059	snp	A/G	3.4212e-05	0.0041358	intron-variant	MYCBP2	GRCh38.p7	13:77146249	AGTCTGAACAATCGT[A/G]AAATCATTTAAAAAC	23077
rs754219129	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77063967	TGAGGATTAACCTAA[A/G]CAATTTTTACCAGCA	23077
rs754242589	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77297306	CATTTCACTTAATAT[A/G]TTTTATGTTCACCAT	23077
rs754243285	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77060216	ATTACAGACCAAGCT[G/T]ATTTTTAAACACAGA	23077
rs754262030	snp	A/G	1.64825e-05	0.00287071	synonymous-codon	MYCBP2	GRCh38.p7	13:77177847	GTCTACTGAAAAACA[A/G]ATTGCATCAGGGGAC	23077
rs754264875	snp	G/T	1.6604e-05	0.00288127	missense	MYCBP2	GRCh38.p7	13:77263726	TTCTAGCCAGTTTAA[G/T]TTGCAATTCTTGCTG	23077
rs754270152	snp	A/T	1.64743e-05	0.00287	missense	MYCBP2	GRCh38.p7	13:77125397	GGACCATGCCTCTCC[A/T]TCATCACTCTCACAG	23077
rs754283675	snp	A/G	1.65031e-05	0.00287251	synonymous-codon	MYCBP2	GRCh38.p7	13:77098511	CATTTTCTTCTTGCG[A/G]AGGGTATCTGGATCA	23077
rs754287689	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77091602	GCCTCAACTCACTAG[A/G]ATGCCCACTCAACTA	23077
rs754287768	snp	C/T			intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77075428	TAACTCCTCAGCATA[C/T]ACTCTCCCACCCTTA	23077
rs754293927	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77283092	ACAAAGTTACTTACT[C/T]ACTGGAGTACAAAGT	23077
rs754294977	snp	A/C	7.97798e-05	0.00631534	synonymous-codon, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77326680	CAGCGCCCCCGGCGC[A/C]GGGGAGGAAGAGAAG	23077
rs754305609	snp	A/C/T	3.32481e-05	0.00407715	intron-variant	MYCBP2	GRCh38.p7	13:77146128	GCAGCTGACAACACA[A/C/T]GTTTTGGTTATACTT	23077
rs754307592	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77309824	ACATTGCTTAAAAAC[A/C]TATGATTGGCTGGGC	23077
rs754316850	in-del	-/GAAGA			intron-variant	MYCBP2	GRCh38.p7	13:77282522	TCTTCACACTCAGAG[-/GAAGA]GAACTTTTCAAAACT	23077
rs754319108	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77210037	TCAACTTACTGGAAT[C/T]TTGCCTACTAAGGCC	23077
rs754329971	snp	C/T	1.64909e-05	0.00287144	synonymous-codon	MYCBP2	GRCh38.p7	13:77055627	TGGGTCATTATAAAA[C/T]CTCACACCAGGAGTT	23077
rs754334565	in-del	-/AAT			intron-variant	MYCBP2	GRCh38.p7	13:77102509	ATTTAAATTTAATTA[-/AAT]AATACTTTAAGACAA	23077
rs754338783	snp	C/T	1.64822e-05	0.00287068	synonymous-codon	MYCBP2	GRCh38.p7	13:77062629	ATCCTTTCCCATCCA[C/T]CTCCCCGAGGAGAGA	23077
rs754350231	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77117106	GTAGTACTTCTAAAT[A/G]TAAAAAGTCTGATGC	23077
rs754352879	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77128617	AGTTTATCCAATTCT[C/T]GTGCTAAACAGTATA	23077
rs754362307	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77236667	AAATAATTTTACACA[G/T]AATATGATTTTGTGT	23077
rs754380849	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77138881	TTCCACACAGCTGTA[A/T]AAATAAGAAAGAAAA	23077
rs754384482	snp	C/T	1.65272e-05	0.0028746	synonymous-codon	MYCBP2	GRCh38.p7	13:77090143	TCTTCTAGGAATAGC[C/T]TTAACTCGTGCAGGT	23077
rs754388017	snp	C/T	4.94572e-05	0.00497254	missense	MYCBP2	GRCh38.p7	13:77166433	GTCAATTTTGGTCCA[C/T]ATCCTGAATTCTGAA	23077
rs754391998	snp	C/T	3.83054e-05	0.00437621	intron-variant	MYCBP2	GRCh38.p7	13:77185863	CATTTAAAAAAAATG[C/T]ATCATACCTGACACT	23077
rs754392462	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77052494	ATGAGCCACATGCCT[C/G]GCCTAAAGCTATTTC	23077
rs754395197	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77244502	TTCCTTACACCTTAT[A/G]CAAAAATTAATTCAA	23077
rs754396493	in-del	-/G			intron-variant	MYCBP2	GRCh38.p7	13:77248797	AAACAGGGTCTCAAA[-/G]GAGCTCCTTGTACAC	23077
rs754402179	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77296205	TGAGAGGATTGCTTG[A/T]GCCCACGAGTTCGAG	23077
rs754406225	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77154079	ATAAAGATTTTAACA[A/G]TTTATGAACAGTCTA	23077
rs754415636	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77067564	GTTTTGGTACTAAAA[C/T]AGAGGCAATAACTAA	23077
rs754426524	snp	A/G	4.33642e-05	0.0046562	intron-variant	MYCBP2	GRCh38.p7	13:77064602	AAACAAAACAAAACA[A/G]AGCAAAACCTACTCT	23077
rs754428241	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77221555	TCCACTCTGGCAAGA[C/G]CATGAAATACTATTT	23077
rs754432744	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77132098	TCTCATTCTGTTTAC[A/G]AAACTTTAACACTAA	23077
rs754443134	snp	G/T	1.65064e-05	0.00287279	synonymous-codon	MYCBP2	GRCh38.p7	13:77185991	ATCCTTTTAATCCTC[G/T]AAGTTCTTCAACTCC	23077
rs754454768	snp	A/G	1.65362e-05	0.00287538	synonymous-codon	MYCBP2	GRCh38.p7	13:77176515	TAAAGGAACCACTTT[A/G]TCAAGTCTGATCTCA	23077
rs754458644	in-del	-/CA			intron-variant	MYCBP2	GRCh38.p7	13:77285918	GAAAGCAAAGGAAGG[-/CA]AAGGAAGGAGCTATT	23077
rs754466452	snp	C/G	3.46927e-05	0.00416475	intron-variant	MYCBP2	GRCh38.p7	13:77174502	TTCCTTCATTATAAA[C/G]ATGTAAAACATCTTT	23077
rs754480042	snp	C/G	1.65007e-05	0.00287229	missense, intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77077260	TCACCATCTTTCCAG[C/G]CCAGGACTTTGACTT	23077
rs754496153	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77147374	ACAATTATGGTAAAA[G/T]GTAAAGACAAAAATG	23077
rs754507361	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77177434	GCAGCCTCAACCTCC[C/T]GGGCTCAAGTGATCC	23077
rs754512922	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77143613	ACTCCATAATTGTGC[A/G]AGCCAATTTCCCTAA	23077
rs754521731	in-del	-/T	1.64738e-05	0.00286995	frameshift-variant	MYCBP2	GRCh38.p7	13:77061769	TGCAGTTTCACCATC[-/T]ATCATGGTTATCACA	23077
rs754523429	snp	C/T	1.64999e-05	0.00287222	synonymous-codon	MYCBP2	GRCh38.p7	13:77166405	CCATGAATTAAGATT[C/T]TCATGAACAGATGTC	23077
rs754526944	snp	C/T	1.64773e-05	0.00287026	synonymous-codon	MYCBP2	GRCh38.p7	13:77243084	CTCTAATCTGTGCCT[C/T]CTGATTACACGTTGC	23077
rs754528503	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77246878	AAGAAACACATGATC[A/G]TCTCAATTGATGTAC	23077
rs754542826	snp	A/G	1.6489e-05	0.00287128	missense	MYCBP2	GRCh38.p7	13:77261320	TCAACCCATTTTCCT[A/G]CTGAAGGACCACCTT	23077
rs754547691	snp	A/T	1.65165e-05	0.00287367	intron-variant	MYCBP2	GRCh38.p7	13:77065979	CTGCCAAAACAGAAG[A/T]ATGGGAACTTACTGC	23077
rs754565850	snp	A/T	1.67301e-05	0.00289219	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77077425	GGAACCTGATTCAGC[A/T]GGATCACTTTTATCA	23077
rs754581721	snp	C/T	1.70382e-05	0.0029187	intron-variant	MYCBP2	GRCh38.p7	13:77140208	AGGAAGAACATAGAA[C/T]AGAGATCTTACAAGT	23077
rs754586550	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77223466	ACCTGAACTAATAAA[G/T]ATGGATTTTCTATTA	23077
rs754586596	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77127698	TCCCTACCAGTAGCC[A/T]CATAATGAAGAGATA	23077
rs754591205	snp	A/T	1.68485e-05	0.00290241	stop-gained	MYCBP2	GRCh38.p7	13:77185110	TAAATTACCTGATCC[A/T]AACAATTCAGCAGAT	23077
rs754600783	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77262445	CTCAAAGTTTTATTG[A/G]GCGTTTATTAGGTAC	23077
rs754607774	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77297619	TAGACAATGTCACTC[C/T]TAAAAATAGAGAAGT	23077
rs754613098	snp	G/T	3.32414e-05	0.00407671	synonymous-codon	MYCBP2	GRCh38.p7	13:77273592	AGCACAGGAAAGTGC[G/T]GTTAAGGACTGTCCT	23077
rs754638820	snp	A/T	6.59174e-05	0.00574059	missense	MYCBP2	GRCh38.p7	13:77051039	TAGGAATGCTAGTCA[A/T]TCTTTGAAAATCATC	23077
rs754641441	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77054063	AGTGAGATGGGGGTA[C/T]GTTACAGAGGAGGTG	23077
rs754648737	in-del	-/AAA			intron-variant	MYCBP2	GRCh38.p7	13:77153065	GCGAGACTCTGTCTC[-/AAA]AAAAAAAAAAAAAAA	23077
rs754649443	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77070115	TATAGCTGGGTATTT[C/G]ACACCAAATAAAAAA	23077
rs754670978	snp	C/T			intron-variant, upstream-variant-2KB	MYCBP2, LOC107984564	GRCh38.p7	13:77325537	CCAACTGAACATCTA[C/T]ATCAAGGAAGCTGAA	23077
rs754672012	snp	C/T	1.65007e-05	0.00287229	synonymous-codon	MYCBP2	GRCh38.p7	13:77161921	CTGCAATGCAGCCTC[C/T]TCAAGAATTTCAAGG	23077
rs754674939	snp	C/T	1.65784e-05	0.00287905	missense	MYCBP2	GRCh38.p7	13:77061277	GAAGGTCAACCTTTA[C/T]AGCTTCTTCTTCTTC	23077
rs754679623	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77323993	CTCTCTCACTTCTTC[A/G]CTCTGTCTCTCCATT	23077
rs754683720	snp	C/T	1.71911e-05	0.00293177	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77082019	GATATATAAGCAATA[C/T]ACGAAATAATTATTT	23077
rs754683927	snp	A/G			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77084849	GACTCCCTTTCTGCA[A/G]CTCTGTACCACTAGT	23077
rs754688319	snp	C/T	1.65985e-05	0.00288079	intron-variant	MYCBP2	GRCh38.p7	13:77233275	GGGCCTGAGGAGAAA[C/T]ATTTTGTATGTGCAT	23077
rs754707142	snp	C/T	1.6477e-05	0.00287024	missense	MYCBP2	GRCh38.p7	13:77140923	TTGGTGGGTCTTTTA[C/T]TTTTACTTCCAGACC	23077
rs754711254	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77212780	AAGTATGGCTCTCTA[C/T]AGGGACCTGGTCAGG	23077
rs754722691	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77185825	AAATCTTCTCAATGT[C/T]TCTAATATTTTCTCC	23077
rs754733261	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77055035	ATATACATGGTAGGT[A/G]AAGGTATAGATGTAA	23077
rs754759281	snp	A/C	0.000198978	0.00997243	intron-variant	MYCBP2	GRCh38.p7	13:77260639	CTCTATGTACAAATA[A/C]TAATAATAATGGTTT	23077
rs754771743	in-del	-/A/AA	0.367199	0.222643	splice-acceptor-variant	MYCBP2	GRCh38.p7	13:77176630	CTGCATGTTCACTCT[-/A/AA]AAAAAAAAAAAATGA	23077
rs754774305	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77068887	AGTTTGATTTACTAC[G/T]CCTAGCAAAACAAGC	23077
rs754783152	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77154512	ATGCAAGATATAAAC[A/G]TACCAGATATCAAAA	23077
rs754795901	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77119622	TACTGTTACAGATAA[C/T]AAAGTTAGATATATT	23077
rs754803874	snp	C/T	1.65075e-05	0.00287289	missense	MYCBP2	GRCh38.p7	13:77260536	ATACCACAATCTTTC[C/T]TTCCATCTTAATTAT	23077
rs754820556	snp	A/G	2.01056e-05	0.00317055	intron-variant	MYCBP2	GRCh38.p7	13:77296571	ATATGAAAAAGTCCT[A/G]TTCCTTATCAATTAC	23077
rs754825866	snp	C/T	1.67511e-05	0.00289401	missense	MYCBP2	GRCh38.p7	13:77058400	TACAGGCTATCTTAG[C/T]GTATTCCTGTTAAAG	23077
rs754839784	snp	A/C	1.6531e-05	0.00287493	missense	MYCBP2	GRCh38.p7	13:77156128	ATGGTGGTAGGCCAA[A/C]CACAACGAATATCAT	23077
rs754839965	snp	A/T	1.68917e-05	0.00290613	intron-variant	MYCBP2	GRCh38.p7	13:77224564	CAGCTTTATTTTTTC[A/T]TTATATGCATTTTAC	23077
rs754855645	snp	A/T			intron-variant	MYCBP2	GRCh38.p7	13:77211120	ATTACCATAAGAGTA[A/T]AACTGCATCAAAACT	23077
rs754856810	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77254388	TGATTTTTTTTTAAC[C/T]GAAAAAAAATGACAA	23077
rs754861311	snp	C/T	1.64857e-05	0.00287099	missense	MYCBP2	GRCh38.p7	13:77166472	ACAGGAATCAACAAA[C/T]GAAGGACATCTTCTG	23077
rs754872505	snp	C/T	1.71114e-05	0.00292496	intron-variant	MYCBP2	GRCh38.p7	13:77181655	ATAAATAAAACCATT[C/T]AGAGTTTTAGTGCCT	23077
rs754873602	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77239663	CTGGCTGTACTCCCC[C/T]AGTTTTTTGTTTCAG	23077
rs754880041	snp	C/T	1.65485e-05	0.00287645	synonymous-codon	MYCBP2	GRCh38.p7	13:77095441	ACTGGGCAACTGAGA[C/T]TGGAATGGCTTTGCA	23077
rs754887433	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77047447	AGGGATTATGCTATG[A/G]TCTGGATGTTTTTGT	23077
rs754897705	snp	A/G	8.2479e-05	0.00642127	synonymous-codon	MYCBP2	GRCh38.p7	13:77098277	TGAACCTTCATCCAC[A/G]CTCTTAAATTCACTG	23077
rs754902229	snp	G/T	1.91745e-05	0.00309627	intron-variant	MYCBP2	GRCh38.p7	13:77189097	AAAGTCCAATGTCAT[G/T]TTTTCTTTTTAAAGT	23077
rs754910176	snp	A/C	1.65419e-05	0.00287588	intron-variant	MYCBP2	GRCh38.p7	13:77269941	AAACAAGGACAAATC[A/C]CATGTTGTAAAAGAT	23077
rs754915194	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77147489	GGTTCAGGTCAAGAT[A/G]TCCAACTGCTCATCT	23077
rs754939377	snp	A/G			intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77082752	TTGGGACATTTAAGT[A/G]ATTTGAGGTAGGAGA	23077
rs754946197	snp	C/G	1.71811e-05	0.00293091	intron-variant	MYCBP2	GRCh38.p7	13:77070754	AAAGAATGAAGTGGT[C/G]TCTTTAAATAAAATT	23077
rs754946242	snp	A/C/T	5.34244e-05	0.00516815	intron-variant	MYCBP2	GRCh38.p7	13:77205621	AACAAAGAAACAAAA[A/C/T]TTAACTCCTTGAAAT	23077
rs754956335	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77214663	GATTCTGTGATGCTG[C/T]GAACATCAGAGTGGA	23077
rs754960567	snp	C/T			intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77073703	CACAGGGTAGAAATC[C/T]AATATACAAAAGTCA	23077
rs754962927	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77313977	CACACCTATCAGAAT[A/G]GCCAAAATCCAGAAC	23077
rs754973053	snp	A/G	1.65051e-05	0.00287267	synonymous-codon	MYCBP2	GRCh38.p7	13:77097800	CATAGACAATACCTT[A/G]TTTTTGTTGATGCTA	23077
rs754985180	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77122994	AGACTAAGAATGGTC[C/T]AGCACCCAGAGTGAA	23077
rs754992266	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77183954	TTCTTCAAAAAACCA[A/G]CTTTTAGCTGTGTTA	23077
rs754993622	snp	C/T	2.25833e-05	0.00336023	intron-variant	MYCBP2	GRCh38.p7	13:77211344	AAAAATATTTATATA[C/T]AATTTTAATATATAT	23077
rs755005580	snp	C/T	1.83656e-05	0.00303026	intron-variant	MYCBP2	GRCh38.p7	13:77263634	ATATAGGGAAAACAC[C/T]TAATTTGCTATCTTA	23077
rs755011316	snp	C/T	6.64011e-05	0.00576161	synonymous-codon	MYCBP2	GRCh38.p7	13:77164515	CCCACCAAGATTGGC[C/T]AATTCTTTTTCCAAT	23077
rs755012835	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77222691	TCAGAAATGCTGGAT[A/G]TAGAATCCACATATG	23077
rs755029165	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77230089	TTACTTATTGATTCA[A/G]TCTATATACTCTGCT	23077
rs755031984	snp	C/G	3.65751e-05	0.00427624	intron-variant	MYCBP2	GRCh38.p7	13:77051939	GAGAAAACACATCTA[C/G]ATTACAGCAGGAAAA	23077
rs755041001	snp	C/T	1.66051e-05	0.00288137	missense	MYCBP2	GRCh38.p7	13:77061765	ATTGCTGCAGTTTCA[C/T]CATCATCATGGTTAT	23077
rs755054576	snp	G/T			intron-variant	MYCBP2	GRCh38.p7	13:77183394	AAAGTTTTTGATAAT[G/T]TTTAAATGGATATGA	23077
rs755063201	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77215146	GTATAACTTAATTTT[C/T]AGCAACATGTAAATG	23077
rs755066500	snp	A/C	1.65499e-05	0.00287657	intron-variant	MYCBP2	GRCh38.p7	13:77165233	TAGCCCTTAGAAACA[A/C]AATCTTCCTTAAAAG	23077
rs755082892	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77265643	ATTCATTACCATCTA[C/T]AAACCTGACAATTTA	23077
rs755086644	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77196029	AAGAATTGGGGGCTA[C/T]TGGGAGTAAGTCTAT	23077
rs755090223	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77315048	AACTTAGAAGTATGA[A/C]ATGAATGAACTTCTC	23077
rs755095870	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77172870	TTCCTGCCTACAAGT[C/T]GCAGTAGCGTAACTT	23077
rs755102141	snp	A/G	3.31862e-05	0.00407333	synonymous-codon, utr-variant-5-prime	MYCBP2	GRCh38.p7	13:77278846	ACTCCTGAGACACAG[A/G]GATGGATGAGAAAAT	23077
rs755103935	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77314318	CTGCACACAGATGTT[C/T]AGAGCAGCTTTATCC	23077
rs755111392	snp	A/G/T			intron-variant	MYCBP2	GRCh38.p7	13:77124419	TTGAATAAAGATGCA[A/G/T]GTTCTCTTATTTACC	23077
rs755112314	snp	C/T			intron-variant	MYCBP2	GRCh38.p7	13:77300677	ACATCACTATGCTTA[C/T]AAAAATAAGCACTCC	23077
rs755131442	in-del	-/G	1.69843e-05	0.00291408	intron-variant	MYCBP2	GRCh38.p7	13:77096268	GTATTTTTATACAGT[-/G]TATCCATATCATTAA	23077
rs755140948	in-del	-/AT	1.68967e-05	0.00290656	intron-variant	MYCBP2	GRCh38.p7	13:77189065	AAAGGCAGTAGACAC[-/AT]ATAAAATTATGTTAG	23077
rs755143483	snp	C/T	4.97294e-05	0.0049862	synonymous-codon	MYCBP2	GRCh38.p7	13:77206678	CAAAGCTGCATGAGA[C/T]CGGGTAGTGAGGGCC	23077
rs755148257	snp	C/G			intron-variant	MYCBP2	GRCh38.p7	13:77137258	AAATCGTGGGATTCA[C/G]AATTGTGACAGATGG	23077
rs755156842	snp	C/T			intron-variant, downstream-variant-500B	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77088207	TACCAAAATATTTTT[C/T]CAAATCACATTTTAC	23077

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