Item | Value |
---|---|
geneid | 100271849 |
ensemblid | ENSG00000213999.17 |
hgncid | 6995 |
symbol | MEF2B |
name | myocyte enhancer factor 2B |
refseq_nuc | NM_001145785.2 |
refseq_prot | NP_001139257.1 |
ensembl_nuc | ENST00000424583.7 |
ensembl_prot | ENSP00000402154.2 |
mane_status | MANE Select |
chr | chr19 |
start | 19145567 |
end | 19170263 |
strand | - |
ver | v1.2 |
region | chr19:19145567-19170263 |
region5000 | chr19:19140567-19175263 |
regionname0 | MEF2B_chr19_19145567_19170263 |
regionname5000 | MEF2B_chr19_19140567_19175263 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 368 | 385 | 84 | 64 | 179 | 14 | 42 | 133 | MEF2B_chr19_19140567_19175263 | MEF2B | MGRKK others(363): Show |
chr19 | 19140567 | 19175263 |
a0002 | 0/0 | 368 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | MGRKK others(363): Show |
chr19 | 19140567 | 19175263 |
a0003 | 0/0 | 368 | 6 | 0 | 0 | 6 | 0 | 0 | 6 | MEF2B_chr19_19140567_19175263 | MEF2B | MGRKK others(363): Show |
chr19 | 19140567 | 19175263 |
a0004 | 0/0 | 368 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | MGRKK others(363): Show |
chr19 | 19140567 | 19175263 |
a0005 | 0/0 | 151 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | MGRKK others(146): Show |
chr19 | 19140567 | 19175263 |
a0006 | 0/0 | 362 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | MGRKK others(357): Show |
chr19 | 19140567 | 19175263 |
a0007 | 0/0 | 368 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | MGRKK others(363): Show |
chr19 | 19140567 | 19175263 |
a0008 | 0/0 | 368 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | MGRKK others(363): Show |
chr19 | 19140567 | 19175263 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1104 | 360 | 78 | 62 | 167 | 14 | 37 | MEF2B_chr19_19140567_19175263 | MEF2B | ATGGG others(1099): Show |
chr19 | 19140567 | 19175263 | ||
a0001c0002 | 0/0 | 1104 | 11 | 0 | 2 | 7 | 0 | 2 | MEF2B_chr19_19140567_19175263 | MEF2B | ATGGG others(1099): Show |
chr19 | 19140567 | 19175263 | ||
a0001c0003 | 0/0 | 1104 | 9 | 1 | 0 | 5 | 0 | 3 | MEF2B_chr19_19140567_19175263 | MEF2B | ATGGG others(1099): Show |
chr19 | 19140567 | 19175263 | ||
a0001c0006 | 0/0 | 1104 | 5 | 5 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | ATGGG others(1099): Show |
chr19 | 19140567 | 19175263 | ||
a0002c0004 | 0/0 | 1104 | 8 | 8 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | ATGGG others(1099): Show |
chr19 | 19140567 | 19175263 | ||
a0003c0005 | 0/0 | 1104 | 6 | 0 | 0 | 6 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | ATGGG others(1099): Show |
chr19 | 19140567 | 19175263 | ||
a0004c0008 | 0/0 | 1104 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | ATGGG others(1099): Show |
chr19 | 19140567 | 19175263 | ||
a0005c0007 | 0/0 | 1104 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | ATGGG others(1099): Show |
chr19 | 19140567 | 19175263 | ||
a0006c0010 | 0/0 | 1086 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | ATGGG others(1081): Show |
chr19 | 19140567 | 19175263 | ||
a0007c0009 | 0/0 | 1104 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | ATGGG others(1099): Show |
chr19 | 19140567 | 19175263 | ||
a0008c0011 | 0/0 | 1104 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | ATGGG others(1099): Show |
chr19 | 19140567 | 19175263 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1425 | 354 | 77 | 62 | 162 | 14 | 37 | MEF2B_chr19_19140567_19175263 | MEF2B | ATCTT others(1420): Show |
chr19 | 19140567 | 19175263 |
a0001c0001t0002 | 0/0 | 1425 | 4 | 0 | 0 | 4 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | ATCTT others(1420): Show |
chr19 | 19140567 | 19175263 |
a0001c0001t0003 | 0/0 | 1425 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | ATCTT others(1420): Show |
chr19 | 19140567 | 19175263 |
a0001c0001t0004 | 0/0 | 1425 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | ATCTT others(1420): Show |
chr19 | 19140567 | 19175263 |
a0001c0002t0001 | 0/0 | 1425 | 11 | 0 | 2 | 7 | 0 | 2 | MEF2B_chr19_19140567_19175263 | MEF2B | ATCTT others(1420): Show |
chr19 | 19140567 | 19175263 |
a0001c0003t0001 | 0/0 | 1425 | 9 | 1 | 0 | 5 | 0 | 3 | MEF2B_chr19_19140567_19175263 | MEF2B | ATCTT others(1420): Show |
chr19 | 19140567 | 19175263 |
a0001c0006t0001 | 0/0 | 1425 | 5 | 5 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | ATCTT others(1420): Show |
chr19 | 19140567 | 19175263 |
a0002c0004t0001 | 0/0 | 1425 | 8 | 8 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | ATCTT others(1420): Show |
chr19 | 19140567 | 19175263 |
a0003c0005t0001 | 0/0 | 1425 | 6 | 0 | 0 | 6 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | ATCTT others(1420): Show |
chr19 | 19140567 | 19175263 |
a0004c0008t0001 | 0/0 | 1425 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | ATCTT others(1420): Show |
chr19 | 19140567 | 19175263 |
a0005c0007t0001 | 0/0 | 1425 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | ATCTT others(1420): Show |
chr19 | 19140567 | 19175263 |
a0006c0010t0001 | 0/0 | 1407 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | ATCTT others(1402): Show |
chr19 | 19140567 | 19175263 |
a0007c0009t0001 | 0/0 | 1425 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | ATCTT others(1420): Show |
chr19 | 19140567 | 19175263 |
a0008c0011t0001 | 0/0 | 1425 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | ATCTT others(1420): Show |
chr19 | 19140567 | 19175263 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 10 | 2 | 3 | 4 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0002 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0004 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0005 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0041 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0127 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0002t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0002t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0003t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0003t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0006t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0006t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0006t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0006t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0001c0006t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0002c0004t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0002c0004t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0002c0004t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0002c0004t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0002c0004t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0002c0004t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0003c0005t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0003c0005t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0003c0005t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0003c0005t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0003c0005t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0003c0005t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0004c0008t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0005c0007t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0006c0010t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0007c0009t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
a0008c0011t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0272 | EUR | GBR | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0201 | EUR | GBR | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0164 | EUR | FIN | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0069 | EUR | FIN | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0031 | EUR | FIN | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0315 | EUR | FIN | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | CHS | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | CHS | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0193 | EAS | CHS | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | CHS | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0224 | AMR | PUR | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | PUR | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01346 | hp2 | a0001 | c0002 | t0001 | g0323 | AMR | CLM | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | CLM | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0332 | EUR | IBS | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0267 | EUR | IBS | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0202 | EUR | IBS | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0280 | EUR | IBS | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0331 | EUR | IBS | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | ACB | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01884 | hp2 | a0001 | c0003 | t0001 | g0054 | AFR | ACB | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0303 | AMR | PEL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PEL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | KHV | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | KHV | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | KHV | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | KHV | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | KHV | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | KHV | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02083 | hp2 | a0001 | c0003 | t0001 | g0161 | EAS | KHV | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | KHV | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | CDX | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02155 | hp2 | a0001 | c0001 | t0004 | g0240 | EAS | CDX | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | CDX | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | CDX | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02257 | hp1 | a0002 | c0004 | t0001 | g0134 | AFR | ACB | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02257 | hp2 | a0001 | c0006 | t0001 | g0042 | AFR | ACB | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02258 | hp2 | a0002 | c0004 | t0001 | g0009 | AFR | ACB | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | ACB | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ACB | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02572 | hp2 | a0002 | c0004 | t0001 | g0095 | AFR | GWD | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0285 | SAS | PJL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02615 | hp1 | a0002 | c0004 | t0001 | g0093 | AFR | GWD | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | GWD | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02622 | hp2 | a0002 | c0004 | t0001 | g0009 | AFR | GWD | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02630 | hp1 | a0002 | c0004 | t0001 | g0094 | AFR | GWD | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0036 | AFR | GWD | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0324 | AFR | GWD | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | GWD | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | GWD | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ESN | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | MSL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ESN | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | ESN | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | ESN | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | MSL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | MSL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0179 | SAS | PJL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | MSL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03453 | hp2 | a0002 | c0004 | t0001 | g0009 | AFR | MSL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0316 | SAS | PJL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0322 | SAS | PJL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | STU | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | STU | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03831 | hp1 | a0004 | c0008 | t0001 | g0237 | SAS | BEB | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03831 | hp2 | a0005 | c0007 | t0001 | g0197 | SAS | BEB | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03834 | hp1 | a0001 | c0003 | t0001 | g0153 | SAS | BEB | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | BEB | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | BEB | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | BEB | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | STU | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG04115 | hp2 | a0001 | c0003 | t0001 | g0053 | SAS | STU | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | BEB | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0275 | SAS | BEB | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | STU | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | STU | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | STU | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | STU | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | YRI | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18522 | hp2 | a0001 | c0006 | t0001 | g0327 | AFR | YRI | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | CHB | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CHB | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | CHB | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | YRI | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | YRI | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18940 | hp1 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18943 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18952 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18954 | hp1 | a0003 | c0005 | t0001 | g0210 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18966 | hp1 | a0001 | c0003 | t0001 | g0172 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18977 | hp2 | a0003 | c0005 | t0001 | g0209 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18978 | hp1 | a0001 | c0003 | t0001 | g0329 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18983 | hp1 | a0001 | c0003 | t0001 | g0155 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18989 | hp1 | a0006 | c0010 | t0001 | g0236 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18989 | hp2 | a0003 | c0005 | t0001 | g0214 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18998 | hp1 | a0007 | c0009 | t0001 | g0248 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19001 | hp1 | a0001 | c0003 | t0001 | g0156 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19003 | hp1 | a0003 | c0005 | t0001 | g0203 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19005 | hp1 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19030 | hp1 | a0001 | c0006 | t0001 | g0052 | AFR | LWK | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | LWK | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19058 | hp1 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19059 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19060 | hp2 | a0003 | c0005 | t0001 | g0212 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19062 | hp2 | a0008 | c0011 | t0001 | g0178 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19063 | hp2 | a0003 | c0005 | t0001 | g0183 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19079 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | YRI | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | YRI | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ASW | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | TSI | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0119 | EUR | TSI | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | GIH | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA20905 | hp2 | a0001 | c0003 | t0001 | g0151 | SAS | GIH | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG02559 | hp2 | a0001 | c0006 | t0001 | g0326 | AFR | ACB | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | MSL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG06807 | hp1 | a0002 | c0004 | t0001 | g0091 | AFR | USA | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | USA | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | USA | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA20300 | hp2 | a0001 | c0006 | t0001 | g0050 | AFR | USA | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | LWK | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | LWK | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0041 | REF | REF | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0127 | REF | REF | MEF2B_chr19_19140567_19175263 | MEF2B | chr19 | 19140567 | 19175263 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:19145811 | C | T | 1 | a0002 | 8 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(5): Show |
missense_variant | MODERATE | c.1093G>A | p.Gly365Ser | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 9/9 | 1181/1425 | 1093/1107 | 365/368 | chr19 | 19145811 | |||
chr19:19145978 | G | A | 1 | a0007 | 1 | NA18998.hp1 | missense_variant | MODERATE | c.926C>T | p.Ala309Val | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 9/9 | 1014/1425 | 926/1107 | 309/368 | chr19 | 19145978 | |||
chr19:19145985 | G | T | 1 | a0003 | 6 | NA18954.hp1 NA18977.hp2 NA18989.hp2 others(3): Show |
missense_variant | MODERATE | c.919C>A | p.Arg307Ser | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 9/9 | 1007/1425 | 919/1107 | 307/368 | chr19 | 19145985 | |||
chr19:19146600 | C | T | 1 | a0004 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.724G>A | p.Gly242Arg | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 7/9 | 812/1425 | 724/1107 | 242/368 | chr19 | 19146600 | |||
chr19:19147006 | CTCACCCC others(40): Show |
C | 1 | a0006 | 1 | NA18989.hp1 | splice_donor_variant&disruptive_inframe_deletion&splice_region_variant&intron_variant | HIGH | c.524_541+29delCCAAA others(42): Show |
p.Pro175_Gly181delin others(4): Show |
MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 5/9 | 524/1107 | 175/368 | chr19 | 19147006 | ||||
chr19:19147121 | A | T | 1 | a0005 | 1 | HG03831.hp2 | stop_gained | HIGH | c.456T>A | p.Cys152* | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 5/9 | 544/1425 | 456/1107 | 152/368 | chr19 | 19147121 | |||
chr19:19149326 | C | G | 1 | a0008 | 1 | NA19062.hp2 | missense_variant | MODERATE | c.158G>C | p.Arg53Pro | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 3/9 | 246/1425 | 158/1107 | 53/368 | chr19 | 19149326 | |||
chr19:19149327 | G | C | 1 | a0008 | 1 | NA19062.hp2 | missense_variant | MODERATE | c.157C>G | p.Arg53Gly | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 3/9 | 245/1425 | 157/1107 | 53/368 | chr19 | 19149327 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:19146574 | G | A | 1 | a0001c0002 | 11 | HG00597.hp1 HG01074.hp2 HG01346.hp2 others(8): Show |
synonymous_variant | LOW | c.750C>T | p.Phe250Phe | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 7/9 | 838/1425 | 750/1107 | 250/368 | chr19 | 19146574 | |||
chr19:19146829 | T | C | 1 | a0001c0003 | 9 | HG01884.hp2 HG02083.hp2 HG03834.hp1 others(6): Show |
synonymous_variant | LOW | c.588A>G | p.Thr196Thr | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 6/9 | 676/1425 | 588/1107 | 196/368 | chr19 | 19146829 | |||
chr19:19146871 | C | T | 1 | a0001c0006 | 5 | HG02257.hp2 HG02559.hp2 NA18522.hp2 others(2): Show |
synonymous_variant | LOW | c.546G>A | p.Leu182Leu | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 6/9 | 634/1425 | 546/1107 | 182/368 | chr19 | 19146871 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:19145650 | G | A | 1 | a0001c0001t0002 | 4 | NA18948.hp2 NA18963.hp2 NA19002.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*147C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 9/9 | 147 | chr19 | 19145650 | ||||||
chr19:19145700 | T | C | 1 | a0001c0001t0004 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*97A>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 9/9 | 97 | chr19 | 19145700 | ||||||
chr19:19170208 | C | G | 1 | a0001c0001t0003 | 1 | HG02717.hp1 | 5_prime_UTR_variant | MODIFIER | c.-33G>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/9 | 19473 | chr19 | 19170208 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:19146061 | G | A | 110 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0014 others(107): Show |
130 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.882-39C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 8/8 | chr19 | 19146061 | |||||||
chr19:19146081 | G | A | 4 | a0001c0001t0001g0105 a0001c0001t0001g0319 a0001c0001t0001g0320 others(1): Show |
4 | HG01884.hp1 HG02280.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.882-59C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 8/8 | chr19 | 19146081 | |||||||
chr19:19146118 | C | T | 3 | a0001c0006t0001g0042 a0001c0006t0001g0050 a0001c0006t0001g0052 |
3 | HG02257.hp2 NA19030.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.882-96G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 8/8 | chr19 | 19146118 | |||||||
chr19:19146141 | G | C | 1 | a0001c0001t0001g0139 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.882-119C>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 8/8 | chr19 | 19146141 | |||||||
chr19:19146142 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.882-120A>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 8/8 | chr19 | 19146142 | |||||||
chr19:19146144 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.882-122G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 8/8 | chr19 | 19146144 | |||||||
chr19:19146672 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0037 |
4 | HG02280.hp2 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.676-24C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 6/8 | chr19 | 19146672 | |||||||
chr19:19146988 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.541+48G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 5/8 | chr19 | 19146988 | |||||||
chr19:19146990 | A | T | 1 | a0001c0001t0001g0102 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.541+46T>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 5/8 | chr19 | 19146990 | |||||||
chr19:19146996 | C | G | 1 | a0001c0001t0001g0027 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.541+40G>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 5/8 | chr19 | 19146996 | |||||||
chr19:19147000 | C | A | 1 | a0001c0001t0001g0102 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.541+36G>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 5/8 | chr19 | 19147000 | |||||||
chr19:19147001 | A | G | 1 | a0001c0001t0001g0102 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.541+35T>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 5/8 | chr19 | 19147001 | |||||||
chr19:19147002 | G | T | 1 | a0001c0001t0001g0102 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.541+34C>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 5/8 | chr19 | 19147002 | |||||||
chr19:19147005 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.541+31G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 5/8 | chr19 | 19147005 | |||||||
chr19:19147006 | C | G | 1 | a0001c0001t0001g0102 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.541+30G>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 5/8 | chr19 | 19147006 | |||||||
chr19:19147016 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.541+20G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 5/8 | chr19 | 19147016 | |||||||
chr19:19147026 | C | G | 1 | a0001c0001t0001g0328 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.541+10G>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 5/8 | chr19 | 19147026 | |||||||
chr19:19147209 | GAGGACCC others(267): Show |
G | 112 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0014 others(109): Show |
132 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.393+215_394-27del | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 4/8 | chr19 | 19147209 | |||||||
chr19:19147576 | A | G | 63 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(60): Show |
82 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.393+122T>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 4/8 | chr19 | 19147576 | |||||||
chr19:19147678 | A | G | 1 | a0001c0001t0001g0256 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.393+20T>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 4/8 | chr19 | 19147678 | |||||||
chr19:19147847 | G | A | 25 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0177 others(22): Show |
32 | HG00140.hp2 HG00438.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.259-15C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 3/8 | chr19 | 19147847 | |||||||
chr19:19147990 | G | C | 6 | a0002c0004t0001g0009 a0002c0004t0001g0091 a0002c0004t0001g0093 others(3): Show |
8 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.259-158C>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 3/8 | chr19 | 19147990 | |||||||
chr19:19148183 | G | A | 43 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(40): Show |
60 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.259-351C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 3/8 | chr19 | 19148183 | |||||||
chr19:19148210 | TC | T | 3 | a0001c0001t0001g0102 a0001c0001t0001g0177 a0006c0010t0001g0236 |
3 | NA18940.hp2 NA18987.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.259-379delG | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 3/8 | chr19 | 19148210 | |||||||
chr19:19148240 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0037 |
4 | HG02280.hp2 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.259-408C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 3/8 | chr19 | 19148240 | |||||||
chr19:19148453 | A | C | 13 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0055 others(10): Show |
15 | HG00738.hp2 HG01123.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.259-621T>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 3/8 | chr19 | 19148453 | |||||||
chr19:19148599 | G | A | 1 | a0001c0003t0001g0161 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.258+627C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 3/8 | chr19 | 19148599 | |||||||
chr19:19148680 | C | CTTAT | 35 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0018 others(32): Show |
44 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.258+542_258+545dup others(4): Show |
MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 3/8 | chr19 | 19148680 | |||||||
chr19:19148680 | CTTAT | C | 104 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(101): Show |
131 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.258+542_258+545del others(4): Show |
MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 3/8 | chr19 | 19148680 | |||||||
chr19:19148680 | CTTATTTA others(5): Show |
C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0131 |
3 | HG03486.hp1 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.258+534_258+545del others(12): Show |
MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 3/8 | chr19 | 19148680 | |||||||
chr19:19148780 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.258+446G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 3/8 | chr19 | 19148780 | |||||||
chr19:19148805 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.258+421C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 3/8 | chr19 | 19148805 | |||||||
chr19:19148869 | A | G | 117 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(114): Show |
147 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.258+357T>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 3/8 | chr19 | 19148869 | |||||||
chr19:19149002 | G | A | 6 | a0002c0004t0001g0009 a0002c0004t0001g0091 a0002c0004t0001g0093 others(3): Show |
8 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.258+224C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 3/8 | chr19 | 19149002 | |||||||
chr19:19149056 | C | T | 3 | a0001c0001t0001g0122 a0001c0001t0001g0139 a0001c0001t0001g0140 |
3 | HG02258.hp1 HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.258+170G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 3/8 | chr19 | 19149056 | |||||||
chr19:19149083 | C | T | 1 | a0008c0011t0001g0178 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.258+143G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 3/8 | chr19 | 19149083 | |||||||
chr19:19149084 | T | C | 1 | a0008c0011t0001g0178 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.258+142A>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 3/8 | chr19 | 19149084 | |||||||
chr19:19149110 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.258+116C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 3/8 | chr19 | 19149110 | |||||||
chr19:19149179 | C | T | 6 | a0002c0004t0001g0009 a0002c0004t0001g0091 a0002c0004t0001g0093 others(3): Show |
8 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.258+47G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 3/8 | chr19 | 19149179 | |||||||
chr19:19149207 | G | T | 1 | a0008c0011t0001g0178 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.258+19C>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 3/8 | chr19 | 19149207 | |||||||
chr19:19149553 | G | A | 10 | a0001c0001t0001g0160 a0001c0003t0001g0053 a0001c0003t0001g0054 others(7): Show |
10 | HG01884.hp2 HG02083.hp2 HG03834.hp1 others(7): Show |
intron_variant | MODIFIER | c.55-124C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19149553 | |||||||
chr19:19149657 | C | G | 10 | a0001c0001t0001g0199 a0001c0002t0001g0011 a0001c0002t0001g0179 others(7): Show |
12 | HG00597.hp1 HG01074.hp2 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.55-228G>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19149657 | |||||||
chr19:19149683 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.55-254G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19149683 | |||||||
chr19:19149742 | G | A | 1 | a0001c0001t0003g0036 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.55-313C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19149742 | |||||||
chr19:19149777 | T | TA | 241 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(238): Show |
291 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(288): Show |
intron_variant | MODIFIER | c.55-349dupT | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19149777 | |||||||
chr19:19149785 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.55-356T>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19149785 | |||||||
chr19:19149838 | G | A | 12 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0048 others(9): Show |
14 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.55-409C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19149838 | |||||||
chr19:19149877 | G | T | 44 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(41): Show |
62 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.55-448C>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19149877 | |||||||
chr19:19149908 | T | C | 100 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(97): Show |
120 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.55-479A>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19149908 | |||||||
chr19:19149946 | G | A | 1 | a0001c0001t0001g0045 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.55-517C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19149946 | |||||||
chr19:19149951 | G | C | 29 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0031 others(26): Show |
37 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.55-522C>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19149951 | |||||||
chr19:19149958 | G | A | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG00738.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.55-529C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19149958 | |||||||
chr19:19149974 | G | A | 154 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(151): Show |
188 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.55-545C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19149974 | |||||||
chr19:19149997 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.55-568T>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19149997 | |||||||
chr19:19149999 | C | T | 49 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(46): Show |
62 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.55-570G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19149999 | |||||||
chr19:19150039 | C | T | 17 | a0001c0001t0001g0076 a0001c0001t0001g0149 a0001c0001t0001g0150 others(14): Show |
17 | HG01884.hp2 HG02083.hp2 HG03834.hp1 others(14): Show |
intron_variant | MODIFIER | c.55-610G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150039 | |||||||
chr19:19150051 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.55-622G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150051 | |||||||
chr19:19150083 | C | CA | 27 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0023 others(24): Show |
33 | HG00639.hp2 HG00738.hp2 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.54+598dupT | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150083 | |||||||
chr19:19150083 | CA | C | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(109): Show |
142 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.54+598delT | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150083 | |||||||
chr19:19150083 | CAA | C | 9 | a0001c0001t0001g0038 a0001c0001t0001g0165 a0001c0001t0001g0182 others(6): Show |
9 | HG01516.hp1 HG02004.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.54+597_54+598delTT | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150083 | |||||||
chr19:19150083 | CAAAAAAA others(2): Show |
C | 35 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0030 others(32): Show |
44 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.54+590_54+598delTT others(7): Show |
MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150083 | |||||||
chr19:19150083 | CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0001g0280 a0001c0002t0001g0233 |
2 | HG01516.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.54+589_54+598delTT others(8): Show |
MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150083 | |||||||
chr19:19150095 | AAAAAAAA others(26): Show |
A | 2 | a0001c0001t0001g0206 a0001c0001t0001g0229 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.54+554_54+586delCC others(31): Show |
MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150095 | |||||||
chr19:19150107 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.54+575C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150107 | |||||||
chr19:19150138 | G | T | 2 | a0001c0001t0001g0206 a0001c0001t0001g0229 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.54+544C>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150138 | |||||||
chr19:19150142 | A | AGGAGGGA others(41): Show |
1 | a0001c0001t0001g0104 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.54+539_54+540insCT others(46): Show |
MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150142 | |||||||
chr19:19150142 | AGGAGGGA others(9): Show |
A | 1 | a0001c0001t0001g0211 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.54+524_54+539delCT others(14): Show |
MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150142 | |||||||
chr19:19150150 | G | T | 2 | a0001c0001t0001g0206 a0001c0001t0001g0229 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.54+532C>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150150 | |||||||
chr19:19150158 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.54+524C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150158 | |||||||
chr19:19150158 | GGGAGGGA others(5): Show |
G | 1 | a0001c0001t0001g0316 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.54+512_54+523delTT others(10): Show |
MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150158 | |||||||
chr19:19150162 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.54+520C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150162 | |||||||
chr19:19150166 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.54+516C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150166 | |||||||
chr19:19150170 | AGGAGGGA others(5): Show |
A | 17 | a0001c0001t0001g0017 a0001c0001t0001g0034 a0001c0001t0001g0122 others(14): Show |
20 | HG01496.hp2 HG01515.hp1 HG01517.hp2 others(17): Show |
intron_variant | MODIFIER | c.54+500_54+511delCT others(10): Show |
MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150170 | |||||||
chr19:19150174 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.54+508C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150174 | |||||||
chr19:19150178 | G | GGGAA | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0324 |
3 | HG02258.hp1 HG02723.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.54+503_54+504insTT others(2): Show |
MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150178 | |||||||
chr19:19150181 | A | G | 1 | a0006c0010t0001g0236 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.54+501T>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150181 | |||||||
chr19:19150182 | G | A | 5 | a0001c0001t0001g0051 a0001c0001t0001g0139 a0001c0001t0001g0140 others(2): Show |
5 | HG02055.hp1 HG02258.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.54+500C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150182 | |||||||
chr19:19150182 | G | GGGAA | 71 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(68): Show |
91 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.54+496_54+499dupTT others(2): Show |
MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150182 | |||||||
chr19:19150182 | G | GGGAAGGA others(5): Show |
1 | a0001c0001t0003g0036 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.54+488_54+499dupTT others(10): Show |
MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150182 | |||||||
chr19:19150182 | G | GGGAAGGA others(65): Show |
1 | a0001c0001t0001g0039 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.54+499_54+500insTT others(70): Show |
MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150182 | |||||||
chr19:19150182 | GGGAA | G | 5 | a0001c0001t0001g0016 a0001c0001t0001g0255 a0001c0001t0001g0269 others(2): Show |
7 | HG00735.hp1 HG01070.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.54+496_54+499delTT others(2): Show |
MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150182 | |||||||
chr19:19150182 | GGGAAGGA others(1): Show |
G | 6 | a0001c0001t0001g0024 a0001c0001t0001g0055 a0001c0001t0001g0056 others(3): Show |
7 | HG01099.hp1 HG01123.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.54+492_54+499delTT others(6): Show |
MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150182 | |||||||
chr19:19150240 | C | T | 2 | a0001c0001t0001g0274 a0001c0001t0001g0285 |
2 | HG02602.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.54+442G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150240 | |||||||
chr19:19150252 | A | G | 2 | a0001c0001t0001g0098 a0001c0001t0001g0198 |
2 | NA19057.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.54+430T>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150252 | |||||||
chr19:19150256 | G | A | 307 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(304): Show |
375 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(372): Show |
intron_variant | MODIFIER | c.54+426C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150256 | |||||||
chr19:19150261 | G | C | 1 | a0001c0001t0001g0008 | 3 | HG02280.hp2 HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.54+421C>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150261 | |||||||
chr19:19150312 | G | A | 5 | a0001c0001t0001g0024 a0001c0001t0001g0055 a0001c0001t0001g0056 others(2): Show |
6 | HG01123.hp1 HG02486.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.54+370C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150312 | |||||||
chr19:19150340 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.54+342G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150340 | |||||||
chr19:19150341 | C | A | 1 | a0001c0001t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.54+341G>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150341 | |||||||
chr19:19150345 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.54+337A>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150345 | |||||||
chr19:19150346 | G | A | 17 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0152 others(14): Show |
17 | HG01884.hp2 HG02083.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.54+336C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150346 | |||||||
chr19:19150370 | C | A | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
288 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(285): Show |
intron_variant | MODIFIER | c.54+312G>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150370 | |||||||
chr19:19150370 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.54+312G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150370 | |||||||
chr19:19150514 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.54+168T>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150514 | |||||||
chr19:19150518 | C | A | 17 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0039 others(14): Show |
22 | HG00639.hp2 HG01167.hp2 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.54+164G>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150518 | |||||||
chr19:19150523 | CA | C | 92 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0021 others(89): Show |
103 | HG00280.hp2 HG00639.hp2 HG01167.hp1 others(100): Show |
intron_variant | MODIFIER | c.54+158delT | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150523 | |||||||
chr19:19150523 | CAA | C | 134 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(131): Show |
166 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.54+157_54+158delTT | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150523 | |||||||
chr19:19150588 | C | T | 5 | a0001c0001t0001g0196 a0001c0006t0001g0042 a0001c0006t0001g0050 others(2): Show |
5 | HG02257.hp2 HG02559.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.54+94G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 2/8 | chr19 | 19150588 | |||||||
chr19:19150922 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-29-158G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19150922 | |||||||
chr19:19150980 | G | A | 3 | a0001c0001t0001g0328 a0001c0006t0001g0326 a0001c0006t0001g0327 |
3 | HG02559.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-29-216C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19150980 | |||||||
chr19:19151024 | A | G | 241 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(238): Show |
292 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.-29-260T>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19151024 | |||||||
chr19:19151042 | T | C | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(82): Show |
112 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.-29-278A>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19151042 | |||||||
chr19:19151094 | A | AATGCAAA others(12): Show |
1 | a0001c0001t0001g0177 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-29-349_-29-331dup others(19): Show |
MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19151094 | |||||||
chr19:19151491 | C | T | 80 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(77): Show |
107 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.-29-727G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19151491 | |||||||
chr19:19151836 | G | C | 1 | a0001c0001t0001g0113 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-29-1072C>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19151836 | |||||||
chr19:19151882 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-29-1118C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19151882 | |||||||
chr19:19151889 | G | A | 81 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(78): Show |
108 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.-29-1125C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19151889 | |||||||
chr19:19151921 | G | T | 130 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0016 others(127): Show |
147 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.-29-1157C>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19151921 | |||||||
chr19:19151950 | C | T | 2 | a0001c0003t0001g0053 a0001c0003t0001g0151 |
2 | HG04115.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-29-1186G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19151950 | |||||||
chr19:19151958 | A | AT | 28 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0049 others(25): Show |
35 | HG00639.hp2 HG01167.hp2 HG01257.hp2 others(32): Show |
intron_variant | MODIFIER | c.-29-1195dupA | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19151958 | |||||||
chr19:19151958 | A | ATT | 78 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0016 others(75): Show |
89 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.-29-1196_-29-1195d others(4): Show |
MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19151958 | |||||||
chr19:19151958 | A | ATTT | 20 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0065 others(17): Show |
24 | HG00738.hp1 HG01167.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.-29-1197_-29-1195d others(5): Show |
MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19151958 | |||||||
chr19:19151958 | ATT | A | 79 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(76): Show |
106 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.-29-1196_-29-1195d others(4): Show |
MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19151958 | |||||||
chr19:19152180 | C | A | 1 | a0001c0001t0001g0235 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-29-1416G>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19152180 | |||||||
chr19:19152180 | C | T | 83 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(80): Show |
110 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.-29-1416G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19152180 | |||||||
chr19:19152188 | C | T | 250 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(247): Show |
303 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.-29-1424G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19152188 | |||||||
chr19:19152287 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-29-1523C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19152287 | |||||||
chr19:19152308 | C | T | 1 | a0001c0001t0001g0191 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-29-1544G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19152308 | |||||||
chr19:19152339 | T | C | 84 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(81): Show |
111 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.-29-1575A>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19152339 | |||||||
chr19:19152358 | G | A | 130 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0016 others(127): Show |
147 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.-29-1594C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19152358 | |||||||
chr19:19152380 | C | CAAAAA | 11 | a0001c0001t0001g0105 a0001c0001t0001g0139 a0001c0001t0001g0140 others(8): Show |
11 | HG02257.hp2 HG02258.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-29-1621_-29-1617d others(7): Show |
MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19152380 | |||||||
chr19:19152380 | C | CAAAAAA | 27 | a0001c0001t0001g0092 a0001c0001t0001g0149 a0001c0001t0001g0150 others(24): Show |
29 | HG01169.hp1 HG01884.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.-29-1622_-29-1617d others(8): Show |
MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19152380 | |||||||
chr19:19152380 | C | CAAAAAAA | 86 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0016 others(83): Show |
101 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.-29-1623_-29-1617d others(9): Show |
MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19152380 | |||||||
chr19:19152387 | A | AAAAAAAG | 7 | a0001c0001t0001g0247 a0001c0001t0001g0276 a0001c0001t0001g0302 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29-1624_-29-1623i others(9): Show |
MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19152387 | |||||||
chr19:19152387 | A | AAAAAAG | 17 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0039 others(14): Show |
22 | HG00639.hp2 HG01167.hp2 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.-29-1629_-29-1624d others(8): Show |
MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19152387 | |||||||
chr19:19152392 | AG | A | 79 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(76): Show |
104 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.-29-1629delC | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19152392 | |||||||
chr19:19152393 | G | A | 1 | a0001c0001t0001g0235 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-29-1629C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19152393 | |||||||
chr19:19152399 | G | A | 1 | a0007c0009t0001g0248 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-29-1635C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19152399 | |||||||
chr19:19152635 | C | T | 2 | a0001c0006t0001g0326 a0001c0006t0001g0327 |
2 | HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-29-1871G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19152635 | |||||||
chr19:19152646 | G | C | 6 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0324 others(3): Show |
6 | HG02258.hp1 HG02559.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29-1882C>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19152646 | |||||||
chr19:19152773 | C | T | 3 | a0001c0006t0001g0042 a0001c0006t0001g0050 a0001c0006t0001g0052 |
3 | HG02257.hp2 NA19030.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-29-2009G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19152773 | |||||||
chr19:19152804 | G | C | 1 | a0001c0001t0001g0102 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-29-2040C>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19152804 | |||||||
chr19:19152805 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-29-2041G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19152805 | |||||||
chr19:19152806 | C | A | 1 | a0001c0001t0001g0102 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-29-2042G>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19152806 | |||||||
chr19:19152807 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-29-2043G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19152807 | |||||||
chr19:19152809 | G | C | 1 | a0001c0001t0001g0102 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-29-2045C>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19152809 | |||||||
chr19:19152815 | T | A | 1 | a0001c0001t0001g0102 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-29-2051A>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19152815 | |||||||
chr19:19152819 | A | T | 1 | a0001c0001t0001g0102 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-29-2055T>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19152819 | |||||||
chr19:19152854 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-29-2090G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19152854 | |||||||
chr19:19152873 | C | T | 2 | a0001c0006t0001g0326 a0001c0006t0001g0327 |
2 | HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-29-2109G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19152873 | |||||||
chr19:19153044 | G | T | 1 | a0001c0001t0001g0158 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-29-2280C>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19153044 | |||||||
chr19:19153072 | T | C | 3 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0245 |
3 | NA18948.hp1 NA18988.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-29-2308A>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19153072 | |||||||
chr19:19153088 | C | A | 1 | a0001c0001t0001g0070 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-29-2324G>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19153088 | |||||||
chr19:19153129 | C | T | 84 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(81): Show |
111 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.-29-2365G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19153129 | |||||||
chr19:19153130 | G | A | 7 | a0001c0001t0001g0092 a0002c0004t0001g0009 a0002c0004t0001g0091 others(4): Show |
9 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-29-2366C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19153130 | |||||||
chr19:19153264 | G | A | 1 | a0001c0001t0001g0190 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-29-2500C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19153264 | |||||||
chr19:19153313 | A | G | 84 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(81): Show |
111 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.-29-2549T>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19153313 | |||||||
chr19:19153447 | T | C | 84 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(81): Show |
111 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.-29-2683A>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19153447 | |||||||
chr19:19153549 | C | T | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0324 |
3 | HG02258.hp1 HG02723.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-29-2785G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19153549 | |||||||
chr19:19153613 | C | T | 3 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 |
3 | HG01884.hp1 HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-29-2849G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19153613 | |||||||
chr19:19153618 | C | G | 84 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(81): Show |
111 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.-29-2854G>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19153618 | |||||||
chr19:19153867 | C | T | 84 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(81): Show |
111 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.-29-3103G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19153867 | |||||||
chr19:19153882 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-29-3118G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19153882 | |||||||
chr19:19153941 | T | TG | 3 | a0001c0001t0001g0154 a0001c0001t0001g0157 a0001c0001t0001g0162 |
3 | HG02559.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-29-3178dupC | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19153941 | |||||||
chr19:19153973 | A | C | 1 | a0001c0001t0001g0192 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-29-3209T>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19153973 | |||||||
chr19:19154031 | G | A | 147 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(144): Show |
169 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(166): Show |
intron_variant | MODIFIER | c.-29-3267C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19154031 | |||||||
chr19:19154124 | T | C | 84 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(81): Show |
111 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.-29-3360A>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19154124 | |||||||
chr19:19154357 | T | C | 241 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(238): Show |
292 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.-29-3593A>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19154357 | |||||||
chr19:19154404 | C | T | 7 | a0001c0001t0001g0092 a0002c0004t0001g0009 a0002c0004t0001g0091 others(4): Show |
9 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-29-3640G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19154404 | |||||||
chr19:19154487 | G | T | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
286 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.-29-3723C>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19154487 | |||||||
chr19:19154769 | G | A | 131 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0016 others(128): Show |
148 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(145): Show |
intron_variant | MODIFIER | c.-29-4005C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19154769 | |||||||
chr19:19154793 | C | T | 2 | a0001c0001t0001g0051 a0001c0001t0001g0105 |
2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.-29-4029G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19154793 | |||||||
chr19:19154921 | C | T | 7 | a0001c0001t0001g0092 a0002c0004t0001g0009 a0002c0004t0001g0091 others(4): Show |
9 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-29-4157G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19154921 | |||||||
chr19:19155518 | A | T | 3 | a0001c0006t0001g0042 a0001c0006t0001g0050 a0001c0006t0001g0052 |
3 | HG02257.hp2 NA19030.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-29-4754T>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19155518 | |||||||
chr19:19155675 | G | T | 1 | a0001c0001t0001g0116 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-29-4911C>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19155675 | |||||||
chr19:19155677 | G | A | 1 | a0001c0001t0001g0230 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-29-4913C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19155677 | |||||||
chr19:19155809 | C | A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0192 |
2 | HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-29-5045G>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19155809 | |||||||
chr19:19155831 | A | AGGGGGGG others(7): Show |
1 | a0001c0001t0001g0246 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-29-5068_-29-5067i others(16): Show |
MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19155831 | |||||||
chr19:19156039 | C | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(91): Show |
121 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.-29-5275G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19156039 | |||||||
chr19:19156063 | G | A | 2 | a0001c0001t0001g0051 a0001c0001t0001g0105 |
2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.-29-5299C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19156063 | |||||||
chr19:19156352 | G | A | 2 | a0001c0003t0001g0155 a0001c0003t0001g0156 |
2 | NA18983.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.-29-5588C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19156352 | |||||||
chr19:19156406 | T | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0043 |
5 | HG02280.hp2 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-29-5642A>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19156406 | |||||||
chr19:19156538 | A | G | 1 | a0001c0001t0001g0324 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-29-5774T>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19156538 | |||||||
chr19:19156592 | A | G | 110 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0016 others(107): Show |
127 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.-29-5828T>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19156592 | |||||||
chr19:19156649 | C | T | 82 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(79): Show |
109 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.-29-5885G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19156649 | |||||||
chr19:19156678 | G | T | 1 | a0001c0001t0001g0232 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-29-5914C>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19156678 | |||||||
chr19:19156691 | G | A | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0324 |
3 | HG02258.hp1 HG02723.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-29-5927C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19156691 | |||||||
chr19:19156744 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-29-5980A>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19156744 | |||||||
chr19:19156993 | A | G | 131 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0016 others(128): Show |
148 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(145): Show |
intron_variant | MODIFIER | c.-29-6229T>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19156993 | |||||||
chr19:19157014 | G | A | 2 | a0001c0001t0001g0250 a0001c0001t0001g0251 |
2 | HG01243.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.-29-6250C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19157014 | |||||||
chr19:19157055 | C | T | 21 | a0001c0001t0001g0051 a0001c0001t0001g0105 a0001c0001t0001g0149 others(18): Show |
21 | HG01884.hp2 HG02055.hp1 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.-29-6291G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19157055 | |||||||
chr19:19157101 | G | A | 82 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(79): Show |
109 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.-29-6337C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19157101 | |||||||
chr19:19157181 | C | T | 238 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(235): Show |
287 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.-29-6417G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19157181 | |||||||
chr19:19157305 | T | C | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(82): Show |
112 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.-29-6541A>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19157305 | |||||||
chr19:19157507 | A | G | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(82): Show |
112 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.-29-6743T>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19157507 | |||||||
chr19:19157590 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-29-6826C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19157590 | |||||||
chr19:19157654 | C | A | 3 | a0001c0006t0001g0042 a0001c0006t0001g0050 a0001c0006t0001g0052 |
3 | HG02257.hp2 NA19030.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-29-6890G>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19157654 | |||||||
chr19:19157666 | A | G | 238 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(235): Show |
287 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.-29-6902T>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19157666 | |||||||
chr19:19157826 | C | T | 3 | a0001c0006t0001g0042 a0001c0006t0001g0050 a0001c0006t0001g0052 |
3 | HG02257.hp2 NA19030.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-29-7062G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19157826 | |||||||
chr19:19157886 | T | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0082 a0001c0001t0001g0228 |
4 | HG00741.hp2 HG01256.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-29-7122A>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19157886 | |||||||
chr19:19157890 | T | C | 91 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(88): Show |
118 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.-29-7126A>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19157890 | |||||||
chr19:19157952 | A | C | 81 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(78): Show |
108 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.-29-7188T>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19157952 | |||||||
chr19:19158065 | G | A | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(82): Show |
112 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.-29-7301C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19158065 | |||||||
chr19:19158092 | CT | C | 91 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(88): Show |
118 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.-29-7329delA | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19158092 | |||||||
chr19:19158108 | A | G | 241 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(238): Show |
292 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.-29-7344T>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19158108 | |||||||
chr19:19158140 | T | C | 1 | a0001c0001t0001g0251 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-29-7376A>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19158140 | |||||||
chr19:19158163 | T | C | 238 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(235): Show |
287 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.-29-7399A>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19158163 | |||||||
chr19:19158221 | G | A | 5 | a0001c0001t0001g0030 a0001c0001t0001g0133 a0001c0001t0001g0204 others(2): Show |
6 | HG01109.hp2 HG02647.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-29-7457C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19158221 | |||||||
chr19:19158378 | C | T | 21 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0039 others(18): Show |
26 | HG00639.hp2 HG01167.hp2 HG01257.hp2 others(23): Show |
intron_variant | MODIFIER | c.-29-7614G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19158378 | |||||||
chr19:19158403 | C | CT | 329 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(326): Show |
401 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(398): Show |
intron_variant | MODIFIER | c.-29-7640dupA | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19158403 | |||||||
chr19:19158405 | A | T | 1 | a0001c0001t0001g0089 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-29-7641T>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19158405 | |||||||
chr19:19158431 | T | G | 3 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 |
3 | HG01884.hp1 HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-29-7667A>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19158431 | |||||||
chr19:19158445 | T | TA | 14 | a0001c0001t0001g0040 a0001c0001t0001g0046 a0001c0001t0001g0048 others(11): Show |
14 | HG00621.hp1 HG01891.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.-29-7682dupT | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19158445 | |||||||
chr19:19158445 | TA | T | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(82): Show |
114 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.-29-7682delT | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19158445 | |||||||
chr19:19158445 | TAA | T | 151 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(148): Show |
172 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(169): Show |
intron_variant | MODIFIER | c.-29-7683_-29-7682d others(4): Show |
MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19158445 | |||||||
chr19:19158485 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0037 |
4 | HG02280.hp2 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-29-7721G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19158485 | |||||||
chr19:19158510 | T | G | 1 | a0001c0001t0001g0058 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-29-7746A>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19158510 | |||||||
chr19:19158538 | A | G | 91 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(88): Show |
118 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.-29-7774T>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19158538 | |||||||
chr19:19158555 | C | CA | 19 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0152 others(16): Show |
19 | HG01884.hp2 HG02083.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.-29-7792dupT | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19158555 | |||||||
chr19:19158595 | GA | G | 80 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(77): Show |
107 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.-29-7832delT | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19158595 | |||||||
chr19:19158619 | G | T | 10 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0055 others(7): Show |
12 | HG00738.hp2 HG01123.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.-29-7855C>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19158619 | |||||||
chr19:19158799 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-29-8035A>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19158799 | |||||||
chr19:19158867 | G | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0043 |
5 | HG02280.hp2 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-29-8103C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19158867 | |||||||
chr19:19158940 | T | G | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(82): Show |
112 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.-29-8176A>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19158940 | |||||||
chr19:19158949 | C | T | 1 | a0001c0001t0001g0226 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-29-8185G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19158949 | |||||||
chr19:19159098 | A | G | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0324 |
3 | HG02258.hp1 HG02723.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-29-8334T>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19159098 | |||||||
chr19:19159131 | G | C | 1 | a0001c0001t0001g0316 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-29-8367C>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19159131 | |||||||
chr19:19159241 | T | TA | 81 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(78): Show |
108 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.-29-8478dupT | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19159241 | |||||||
chr19:19159241 | T | TAA | 50 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0021 others(47): Show |
57 | HG00438.hp2 HG00639.hp2 HG01167.hp2 others(54): Show |
intron_variant | MODIFIER | c.-29-8479_-29-8478d others(4): Show |
MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19159241 | |||||||
chr19:19159241 | T | TAAA | 92 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0014 others(89): Show |
109 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.-29-8480_-29-8478d others(5): Show |
MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19159241 | |||||||
chr19:19159241 | T | TAAAA | 23 | a0001c0001t0001g0043 a0001c0001t0001g0051 a0001c0001t0001g0116 others(20): Show |
23 | HG00408.hp2 HG00735.hp1 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.-29-8481_-29-8478d others(6): Show |
MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19159241 | |||||||
chr19:19159241 | TA | T | 7 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0146 others(4): Show |
7 | HG02004.hp1 HG02257.hp2 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29-8478delT | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19159241 | |||||||
chr19:19159242 | A | T | 1 | a0001c0001t0001g0070 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-29-8478T>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19159242 | |||||||
chr19:19159501 | AG | A | 3 | a0001c0006t0001g0042 a0001c0006t0001g0050 a0001c0006t0001g0052 |
3 | HG02257.hp2 NA19030.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-29-8738delC | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19159501 | |||||||
chr19:19159516 | G | A | 1 | a0001c0001t0001g0312 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-29-8752C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19159516 | |||||||
chr19:19159520 | T | C | 25 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(22): Show |
35 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.-29-8756A>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19159520 | |||||||
chr19:19159849 | T | A | 95 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0016 others(92): Show |
110 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.-29-9085A>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19159849 | |||||||
chr19:19159967 | C | CT | 25 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0059 others(22): Show |
26 | HG00140.hp1 HG00621.hp1 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.-29-9204dupA | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19159967 | |||||||
chr19:19159967 | CT | C | 11 | a0001c0001t0001g0118 a0001c0001t0001g0132 a0001c0001t0001g0139 others(8): Show |
11 | HG02258.hp1 HG02559.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.-29-9204delA | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19159967 | |||||||
chr19:19160159 | G | A | 19 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0152 others(16): Show |
19 | HG01884.hp2 HG02083.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.-29-9395C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19160159 | |||||||
chr19:19160517 | G | A | 19 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0152 others(16): Show |
19 | HG01884.hp2 HG02083.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.-30+9688C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19160517 | |||||||
chr19:19160522 | G | C | 1 | a0001c0001t0001g0217 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-30+9683C>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19160522 | |||||||
chr19:19160595 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-30+9610G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19160595 | |||||||
chr19:19160687 | G | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0043 |
5 | HG02280.hp2 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-30+9518C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19160687 | |||||||
chr19:19160689 | C | G | 188 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(185): Show |
230 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.-30+9516G>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19160689 | |||||||
chr19:19160715 | C | T | 1 | a0001c0001t0001g0292 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-30+9490G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19160715 | |||||||
chr19:19160884 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-30+9321C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19160884 | |||||||
chr19:19160986 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-30+9219G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19160986 | |||||||
chr19:19161004 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-30+9201G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19161004 | |||||||
chr19:19161024 | C | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0043 |
5 | HG02280.hp2 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-30+9181G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19161024 | |||||||
chr19:19161028 | C | T | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG00738.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.-30+9177G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19161028 | |||||||
chr19:19161043 | T | G | 1 | a0001c0001t0001g0096 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-30+9162A>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19161043 | |||||||
chr19:19161106 | C | T | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | HG01978.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-30+9099G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19161106 | |||||||
chr19:19161198 | T | G | 4 | a0001c0001t0001g0051 a0001c0006t0001g0042 a0001c0006t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02257.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+9007A>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19161198 | |||||||
chr19:19161283 | G | A | 1 | a0001c0002t0001g0224 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-30+8922C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19161283 | |||||||
chr19:19161382 | C | T | 100 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0016 others(97): Show |
115 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.-30+8823G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19161382 | |||||||
chr19:19161428 | T | C | 25 | a0001c0001t0001g0051 a0001c0001t0001g0105 a0001c0001t0001g0118 others(22): Show |
25 | HG01884.hp2 HG02055.hp1 HG02083.hp2 others(22): Show |
intron_variant | MODIFIER | c.-30+8777A>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19161428 | |||||||
chr19:19161519 | C | T | 1 | a0001c0001t0001g0045 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-30+8686G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19161519 | |||||||
chr19:19161562 | C | A | 3 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 |
3 | NA18943.hp1 NA18980.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.-30+8643G>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19161562 | |||||||
chr19:19161637 | G | A | 32 | a0001c0001t0001g0033 a0001c0001t0001g0035 a0001c0001t0001g0065 others(29): Show |
34 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.-30+8568C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19161637 | |||||||
chr19:19161678 | C | A | 1 | a0001c0001t0003g0036 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-30+8527G>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19161678 | |||||||
chr19:19161811 | G | GT | 9 | a0001c0001t0001g0044 a0001c0001t0001g0055 a0001c0001t0001g0167 others(6): Show |
9 | HG02074.hp2 HG02135.hp1 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.-30+8393dupA | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19161811 | |||||||
chr19:19161811 | G | T | 1 | a0001c0001t0001g0139 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-30+8394C>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19161811 | |||||||
chr19:19161869 | G | T | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0324 |
3 | HG02258.hp1 HG02723.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-30+8336C>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19161869 | |||||||
chr19:19161980 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-30+8225C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19161980 | |||||||
chr19:19162006 | C | T | 1 | a0001c0001t0001g0328 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-30+8199G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19162006 | |||||||
chr19:19162095 | C | G | 1 | a0001c0001t0001g0030 | 2 | HG02723.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-30+8110G>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19162095 | |||||||
chr19:19162127 | A | AT | 21 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0039 others(18): Show |
26 | HG00639.hp2 HG01167.hp2 HG01257.hp2 others(23): Show |
intron_variant | MODIFIER | c.-30+8077dupA | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19162127 | |||||||
chr19:19162229 | C | A | 1 | a0001c0001t0001g0029 | 2 | HG02922.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-30+7976G>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19162229 | |||||||
chr19:19162314 | G | T | 93 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0016 others(90): Show |
108 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.-30+7891C>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19162314 | |||||||
chr19:19162319 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-30+7886C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19162319 | |||||||
chr19:19162430 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-30+7775G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19162430 | |||||||
chr19:19162479 | T | G | 94 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0016 others(91): Show |
109 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.-30+7726A>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19162479 | |||||||
chr19:19162528 | C | T | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(86): Show |
116 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.-30+7677G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19162528 | |||||||
chr19:19162657 | T | C | 2 | a0001c0001t0001g0222 a0001c0001t0001g0223 |
2 | HG00558.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.-30+7548A>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19162657 | |||||||
chr19:19162676 | G | T | 1 | a0001c0001t0001g0118 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-30+7529C>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19162676 | |||||||
chr19:19162686 | G | C | 1 | a0001c0001t0002g0088 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-30+7519C>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19162686 | |||||||
chr19:19162730 | C | T | 56 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0021 others(53): Show |
65 | HG00639.hp2 HG01167.hp2 HG01257.hp2 others(62): Show |
intron_variant | MODIFIER | c.-30+7475G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19162730 | |||||||
chr19:19163266 | C | T | 24 | a0001c0001t0001g0051 a0001c0001t0001g0105 a0001c0001t0001g0149 others(21): Show |
24 | HG01884.hp2 HG02055.hp1 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.-30+6939G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19163266 | |||||||
chr19:19163283 | G | A | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(86): Show |
116 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.-30+6922C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19163283 | |||||||
chr19:19163338 | C | T | 248 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(245): Show |
301 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.-30+6867G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19163338 | |||||||
chr19:19163344 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-30+6861G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19163344 | |||||||
chr19:19163345 | T | C | 1 | a0001c0001t0001g0107 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-30+6860A>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19163345 | |||||||
chr19:19163346 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-30+6859G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19163346 | |||||||
chr19:19163352 | G | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0037 |
4 | HG02280.hp2 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+6853C>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19163352 | |||||||
chr19:19163446 | G | A | 2 | a0001c0001t0001g0302 a0001c0001t0001g0313 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-30+6759C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19163446 | |||||||
chr19:19163579 | C | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0043 |
5 | HG02280.hp2 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-30+6626G>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19163579 | |||||||
chr19:19163581 | C | G | 2 | a0001c0001t0001g0176 a0001c0001t0001g0271 |
2 | HG02040.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.-30+6624G>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19163581 | |||||||
chr19:19163647 | TTC | T | 21 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0039 others(18): Show |
26 | HG00639.hp2 HG01167.hp2 HG01257.hp2 others(23): Show |
intron_variant | MODIFIER | c.-30+6556_-30+6557d others(4): Show |
MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19163647 | |||||||
chr19:19163717 | A | G | 1 | a0001c0001t0001g0112 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-30+6488T>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19163717 | |||||||
chr19:19163732 | C | A | 1 | a0001c0002t0001g0224 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-30+6473G>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19163732 | |||||||
chr19:19163798 | C | T | 1 | a0001c0001t0001g0328 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-30+6407G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19163798 | |||||||
chr19:19163913 | C | T | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(86): Show |
116 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.-30+6292G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19163913 | |||||||
chr19:19163966 | G | C | 5 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
5 | HG02809.hp2 HG02895.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-30+6239C>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19163966 | |||||||
chr19:19164060 | G | A | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(86): Show |
116 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.-30+6145C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19164060 | |||||||
chr19:19164069 | C | T | 2 | a0001c0006t0001g0326 a0001c0006t0001g0327 |
2 | HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-30+6136G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19164069 | |||||||
chr19:19164105 | C | T | 7 | a0001c0001t0001g0016 a0001c0001t0001g0250 a0001c0001t0001g0251 others(4): Show |
9 | HG00735.hp1 HG01070.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-30+6100G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19164105 | |||||||
chr19:19164124 | T | A | 1 | a0001c0003t0001g0161 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-30+6081A>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19164124 | |||||||
chr19:19164222 | C | G | 89 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0016 others(86): Show |
104 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.-30+5983G>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19164222 | |||||||
chr19:19164233 | G | A | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(86): Show |
116 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.-30+5972C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19164233 | |||||||
chr19:19164462 | G | A | 1 | a0001c0001t0001g0238 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-30+5743C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19164462 | |||||||
chr19:19164504 | C | T | 83 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(80): Show |
110 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.-30+5701G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19164504 | |||||||
chr19:19164542 | G | A | 22 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0039 others(19): Show |
27 | HG00639.hp2 HG01167.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-30+5663C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19164542 | |||||||
chr19:19164545 | G | A | 3 | a0001c0001t0001g0328 a0001c0006t0001g0326 a0001c0006t0001g0327 |
3 | HG02559.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-30+5660C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19164545 | |||||||
chr19:19164576 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-30+5629C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19164576 | |||||||
chr19:19164669 | C | G | 1 | a0008c0011t0001g0178 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-30+5536G>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19164669 | |||||||
chr19:19164670 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-30+5535G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19164670 | |||||||
chr19:19164671 | G | C | 1 | a0008c0011t0001g0178 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-30+5534C>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19164671 | |||||||
chr19:19164687 | G | A | 89 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0016 others(86): Show |
104 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.-30+5518C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19164687 | |||||||
chr19:19164898 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-30+5307G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19164898 | |||||||
chr19:19164926 | C | T | 87 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(84): Show |
114 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.-30+5279G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19164926 | |||||||
chr19:19164993 | C | T | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(86): Show |
116 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.-30+5212G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19164993 | |||||||
chr19:19165016 | C | A | 1 | a0001c0001t0001g0049 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-30+5189G>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19165016 | |||||||
chr19:19165038 | G | A | 3 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0265 |
3 | HG02451.hp2 HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-30+5167C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19165038 | |||||||
chr19:19165055 | C | T | 24 | a0001c0001t0001g0051 a0001c0001t0001g0105 a0001c0001t0001g0149 others(21): Show |
24 | HG01884.hp2 HG02055.hp1 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.-30+5150G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19165055 | |||||||
chr19:19165082 | T | C | 1 | a0001c0001t0001g0230 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-30+5123A>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19165082 | |||||||
chr19:19165226 | C | T | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(86): Show |
116 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.-30+4979G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19165226 | |||||||
chr19:19165229 | C | G | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(86): Show |
116 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.-30+4976G>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19165229 | |||||||
chr19:19165308 | G | A | 1 | a0001c0001t0001g0043 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-30+4897C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19165308 | |||||||
chr19:19165333 | C | T | 3 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0265 |
3 | HG02451.hp2 HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-30+4872G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19165333 | |||||||
chr19:19165375 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-30+4830C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19165375 | |||||||
chr19:19165475 | A | C | 5 | a0001c0001t0001g0024 a0001c0001t0001g0055 a0001c0001t0001g0056 others(2): Show |
6 | HG01123.hp1 HG02486.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30+4730T>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19165475 | |||||||
chr19:19165550 | A | G | 253 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(250): Show |
308 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(305): Show |
intron_variant | MODIFIER | c.-30+4655T>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19165550 | |||||||
chr19:19165559 | G | A | 2 | a0001c0006t0001g0042 a0001c0006t0001g0052 |
2 | HG02257.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-30+4646C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19165559 | |||||||
chr19:19166085 | G | A | 1 | a0001c0001t0001g0317 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-30+4120C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19166085 | |||||||
chr19:19166183 | G | A | 23 | a0001c0001t0001g0051 a0001c0001t0001g0105 a0001c0001t0001g0149 others(20): Show |
23 | HG01884.hp2 HG02055.hp1 HG02083.hp2 others(20): Show |
intron_variant | MODIFIER | c.-30+4022C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19166183 | |||||||
chr19:19166191 | G | A | 93 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0015 others(90): Show |
110 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.-30+4014C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19166191 | |||||||
chr19:19166308 | T | A | 1 | a0001c0001t0001g0089 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-30+3897A>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19166308 | |||||||
chr19:19166487 | G | A | 190 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(187): Show |
238 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.-30+3718C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19166487 | |||||||
chr19:19166580 | A | AC | 198 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(195): Show |
246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.-30+3624dupG | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19166580 | |||||||
chr19:19166592 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-30+3613G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19166592 | |||||||
chr19:19166593 | C | T | 203 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(200): Show |
251 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.-30+3612G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19166593 | |||||||
chr19:19166597 | T | TA | 10 | a0001c0001t0001g0019 a0001c0001t0001g0033 a0001c0001t0001g0090 others(7): Show |
12 | HG00597.hp2 HG00741.hp2 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.-30+3607dupT | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19166597 | |||||||
chr19:19166597 | T | TAA | 172 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(169): Show |
217 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.-30+3606_-30+3607d others(4): Show |
MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19166597 | |||||||
chr19:19166597 | T | TAAA | 10 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0231 others(7): Show |
10 | HG01978.hp2 HG02165.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-30+3605_-30+3607d others(5): Show |
MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19166597 | |||||||
chr19:19166607 | A | AAAAAAAA others(6): Show |
1 | a0008c0011t0001g0178 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-30+3597_-30+3598i others(15): Show |
MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19166607 | |||||||
chr19:19166672 | T | A | 1 | a0001c0001t0001g0328 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-30+3533A>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19166672 | |||||||
chr19:19166674 | G | A | 1 | a0001c0001t0001g0328 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-30+3531C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19166674 | |||||||
chr19:19166686 | G | A | 4 | a0001c0001t0001g0051 a0001c0001t0001g0162 a0001c0006t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02559.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+3519C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19166686 | |||||||
chr19:19166707 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-30+3498G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19166707 | |||||||
chr19:19166708 | A | G | 241 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(238): Show |
294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.-30+3497T>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19166708 | |||||||
chr19:19166732 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-30+3473G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19166732 | |||||||
chr19:19166930 | G | A | 1 | a0001c0006t0001g0327 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-30+3275C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19166930 | |||||||
chr19:19166970 | A | G | 96 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(93): Show |
125 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.-30+3235T>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19166970 | |||||||
chr19:19167062 | G | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0006t0001g0042 |
5 | HG02257.hp2 HG02280.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-30+3143C>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19167062 | |||||||
chr19:19167221 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-30+2984G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19167221 | |||||||
chr19:19167299 | C | T | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(174): Show |
221 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.-30+2906G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19167299 | |||||||
chr19:19167324 | C | G | 1 | a0001c0001t0001g0324 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-30+2881G>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19167324 | |||||||
chr19:19167350 | C | CA | 13 | a0001c0001t0001g0004 a0001c0001t0001g0049 a0001c0001t0001g0135 others(10): Show |
17 | HG00639.hp2 HG01167.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.-30+2854dupT | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19167350 | |||||||
chr19:19167350 | CA | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0019 others(83): Show |
99 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.-30+2854delT | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19167350 | |||||||
chr19:19167350 | CAA | C | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(146): Show |
191 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.-30+2853_-30+2854d others(4): Show |
MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19167350 | |||||||
chr19:19167350 | CAAA | C | 13 | a0001c0001t0001g0014 a0001c0001t0001g0181 a0001c0001t0001g0182 others(10): Show |
15 | HG01169.hp1 HG01255.hp1 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.-30+2852_-30+2854d others(5): Show |
MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19167350 | |||||||
chr19:19167375 | AG | A | 90 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0015 others(87): Show |
107 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.-30+2829delC | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19167375 | |||||||
chr19:19167378 | T | C | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | HG03942.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-30+2827A>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19167378 | |||||||
chr19:19167431 | A | G | 90 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0015 others(87): Show |
107 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.-30+2774T>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19167431 | |||||||
chr19:19167527 | C | CAAAG | 23 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0147 others(20): Show |
23 | HG01123.hp1 HG01884.hp2 HG02083.hp2 others(20): Show |
intron_variant | MODIFIER | c.-30+2674_-30+2677d others(6): Show |
MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19167527 | |||||||
chr19:19167531 | G | A | 90 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0015 others(87): Show |
107 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.-30+2674C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19167531 | |||||||
chr19:19167551 | G | A | 88 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(85): Show |
115 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.-30+2654C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19167551 | |||||||
chr19:19167742 | C | T | 1 | a0001c0003t0001g0053 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-30+2463G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19167742 | |||||||
chr19:19167743 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-30+2462C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19167743 | |||||||
chr19:19167747 | A | G | 3 | a0001c0001t0001g0051 a0001c0006t0001g0050 a0001c0006t0001g0052 |
3 | HG02055.hp1 NA19030.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-30+2458T>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19167747 | |||||||
chr19:19167809 | G | A | 1 | a0004c0008t0001g0237 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-30+2396C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19167809 | |||||||
chr19:19168040 | A | T | 1 | a0001c0001t0001g0049 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-30+2165T>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19168040 | |||||||
chr19:19168213 | G | C | 1 | a0001c0001t0001g0328 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-30+1992C>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19168213 | |||||||
chr19:19168268 | C | CT | 10 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(7): Show |
12 | HG02135.hp2 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.-30+1936dupA | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19168268 | |||||||
chr19:19168268 | CT | C | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(173): Show |
220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.-30+1936delA | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19168268 | |||||||
chr19:19168268 | CTT | C | 18 | a0001c0001t0001g0173 a0001c0001t0001g0176 a0001c0001t0001g0238 others(15): Show |
18 | HG00323.hp2 HG01884.hp1 HG02155.hp1 others(15): Show |
intron_variant | MODIFIER | c.-30+1935_-30+1936d others(4): Show |
MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19168268 | |||||||
chr19:19168271 | T | C | 2 | a0001c0001t0001g0174 a0001c0001t0001g0246 |
2 | NA18979.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.-30+1934A>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19168271 | |||||||
chr19:19168272 | T | C | 1 | a0001c0001t0001g0318 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-30+1933A>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19168272 | |||||||
chr19:19168273 | T | C | 3 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 |
3 | HG01884.hp1 HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-30+1932A>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19168273 | |||||||
chr19:19168343 | C | A | 1 | a0001c0001t0001g0175 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-30+1862G>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19168343 | |||||||
chr19:19168344 | G | A | 87 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(84): Show |
114 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.-30+1861C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19168344 | |||||||
chr19:19168431 | G | A | 1 | a0001c0001t0001g0322 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-30+1774C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19168431 | |||||||
chr19:19168558 | C | A | 90 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0015 others(87): Show |
107 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.-30+1647G>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19168558 | |||||||
chr19:19168596 | T | C | 1 | a0001c0001t0001g0325 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-30+1609A>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19168596 | |||||||
chr19:19168599 | TG | T | 4 | a0001c0001t0001g0177 a0001c0001t0001g0247 a0001c0001t0001g0249 others(1): Show |
4 | HG02897.hp1 NA18987.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+1605delC | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19168599 | |||||||
chr19:19168600 | G | T | 216 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(213): Show |
265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.-30+1605C>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19168600 | |||||||
chr19:19168628 | C | G | 87 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(84): Show |
114 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.-30+1577G>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19168628 | |||||||
chr19:19168643 | C | G | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(174): Show |
221 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.-30+1562G>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19168643 | |||||||
chr19:19168728 | G | A | 1 | a0001c0001t0003g0036 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-30+1477C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19168728 | |||||||
chr19:19168769 | A | G | 1 | a0001c0001t0001g0040 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-30+1436T>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19168769 | |||||||
chr19:19168936 | A | C | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(174): Show |
221 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.-30+1269T>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19168936 | |||||||
chr19:19168984 | A | G | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(174): Show |
221 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.-30+1221T>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19168984 | |||||||
chr19:19168988 | G | A | 1 | a0001c0002t0001g0323 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-30+1217C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19168988 | |||||||
chr19:19169060 | T | A | 1 | a0001c0001t0002g0088 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-30+1145A>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19169060 | |||||||
chr19:19169329 | G | A | 1 | a0001c0001t0001g0324 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-30+876C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19169329 | |||||||
chr19:19169331 | G | A | 1 | a0001c0001t0001g0325 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-30+874C>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19169331 | |||||||
chr19:19169351 | CA | C | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(173): Show |
220 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.-30+853delT | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19169351 | |||||||
chr19:19169493 | G | C | 3 | a0001c0001t0001g0328 a0001c0006t0001g0326 a0001c0006t0001g0327 |
3 | HG02559.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-30+712C>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19169493 | |||||||
chr19:19169498 | C | T | 1 | a0001c0001t0001g0039 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-30+707G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19169498 | |||||||
chr19:19169515 | C | T | 1 | a0001c0001t0001g0019 | 2 | HG00741.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.-30+690G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19169515 | |||||||
chr19:19169586 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-30+619G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19169586 | |||||||
chr19:19169690 | T | C | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(174): Show |
221 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.-30+515A>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19169690 | |||||||
chr19:19169726 | T | A | 1 | a0001c0003t0001g0329 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-30+479A>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19169726 | |||||||
chr19:19169755 | A | C | 1 | a0001c0001t0001g0038 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-30+450T>G | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19169755 | |||||||
chr19:19169773 | A | G | 1 | a0001c0001t0001g0037 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-30+432T>C | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19169773 | |||||||
chr19:19169799 | C | A | 1 | a0001c0001t0001g0330 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-30+406G>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19169799 | |||||||
chr19:19169883 | C | T | 1 | a0001c0001t0003g0036 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-30+322G>A | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19169883 | |||||||
chr19:19170039 | C | A | 2 | a0001c0001t0001g0331 a0001c0001t0001g0332 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-30+166G>T | MEF2B | ENSG00000213999.17 | transcript | ENST00000424583.7 | protein_coding | 1/8 | chr19 | 19170039 |