geneid | 4208 |
---|---|
ensemblid | ENSG00000081189.17 |
hgncid | 6996 |
symbol | MEF2C |
name | myocyte enhancer factor 2C |
refseq_nuc | NM_002397.5 |
refseq_prot | NP_002388.2 |
ensembl_nuc | ENST00000504921.7 |
ensembl_prot | ENSP00000421925.5 |
mane_status | MANE Select |
chr | chr5 |
start | 88717117 |
end | 88883184 |
strand | - |
ver | v1.2 |
region | chr5:88717117-88883184 |
region5000 | chr5:88712117-88888184 |
regionname0 | MEF2C_chr5_88717117_88883184 |
regionname5000 | MEF2C_chr5_88712117_88888184 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 473 | 302 | 78 | 56 | 122 | 14 | 30 | 98 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1422 | 302 | 78 | 56 | 122 | 14 | 30 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 5860 | 78 | 11 | 17 | 37 | 4 | 9 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
t0002 | 0/0 | 5861 | 71 | 17 | 6 | 37 | 1 | 10 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
t0003 | 1/0 | 5860 | 54 | 6 | 15 | 26 | 2 | 4 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
t0004 | 0/1 | 5859 | 35 | 21 | 8 | 0 | 3 | 2 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
t0005 | 0/0 | 5859 | 5 | 4 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
t0006 | 0/0 | 5860 | 5 | 0 | 0 | 5 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
t0007 | 0/0 | 5860 | 5 | 5 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
t0008 | 0/0 | 5861 | 5 | 0 | 2 | 3 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
t0009 | 0/0 | 5859 | 4 | 0 | 1 | 3 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
t0010 | 0/0 | 5862 | 3 | 0 | 0 | 0 | 2 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
t0011 | 0/0 | 5861 | 3 | 0 | 0 | 3 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
t0012 | 0/0 | 5860 | 3 | 0 | 3 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
t0013 | 0/0 | 5860 | 3 | 0 | 0 | 3 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
t0014 | 0/0 | 5859 | 2 | 2 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
t0015 | 0/0 | 5860 | 2 | 2 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
t0016 | 0/0 | 5861 | 2 | 0 | 0 | 0 | 2 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
t0017 | 0/0 | 5860 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
t0018 | 0/0 | 5860 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
t0019 | 0/0 | 5860 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
t0020 | 0/0 | 5859 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
t0021 | 0/0 | 5861 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
t0022 | 0/0 | 5861 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
t0023 | 0/0 | 5861 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
t0024 | 0/0 | 5861 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
t0025 | 0/0 | 5860 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
t0026 | 0/0 | 5860 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
t0027 | 0/0 | 5860 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
t0028 | 0/0 | 5860 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
t0029 | 0/0 | 5861 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
t0030 | 0/0 | 5861 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
t0031 | 0/0 | 5860 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
t0032 | 0/0 | 5860 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
t0033 | 0/0 | 5860 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
t0034 | 0/0 | 5860 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
t0035 | 0/0 | 5860 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
t0036 | 0/0 | 5859 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
t0037 | 0/0 | 5860 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
t0038 | 0/0 | 5860 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0115 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0165 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1422 | 302 | 78 | 56 | 122 | 14 | 30 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 7281 | 78 | 11 | 17 | 37 | 4 | 9 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
a0001c0001t0002 | 0/0 | 7282 | 71 | 17 | 6 | 37 | 1 | 10 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
a0001c0001t0003 | 1/0 | 7281 | 54 | 6 | 15 | 26 | 2 | 4 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
a0001c0001t0004 | 0/1 | 7280 | 35 | 21 | 8 | 0 | 3 | 2 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
a0001c0001t0005 | 0/0 | 7280 | 5 | 4 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
a0001c0001t0006 | 0/0 | 7281 | 5 | 0 | 0 | 5 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
a0001c0001t0007 | 0/0 | 7281 | 5 | 5 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
a0001c0001t0008 | 0/0 | 7282 | 5 | 0 | 2 | 3 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
a0001c0001t0009 | 0/0 | 7280 | 4 | 0 | 1 | 3 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
a0001c0001t0010 | 0/0 | 7283 | 3 | 0 | 0 | 0 | 2 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
a0001c0001t0011 | 0/0 | 7282 | 3 | 0 | 0 | 3 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
a0001c0001t0012 | 0/0 | 7281 | 3 | 0 | 3 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
a0001c0001t0013 | 0/0 | 7281 | 3 | 0 | 0 | 3 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
a0001c0001t0014 | 0/0 | 7280 | 2 | 2 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
a0001c0001t0015 | 0/0 | 7281 | 2 | 2 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
a0001c0001t0016 | 0/0 | 7282 | 2 | 0 | 0 | 0 | 2 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
a0001c0001t0017 | 0/0 | 7281 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
a0001c0001t0018 | 0/0 | 7281 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
a0001c0001t0019 | 0/0 | 7281 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
a0001c0001t0020 | 0/0 | 7280 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
a0001c0001t0021 | 0/0 | 7282 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
a0001c0001t0022 | 0/0 | 7282 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
a0001c0001t0023 | 0/0 | 7282 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
a0001c0001t0024 | 0/0 | 7282 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
a0001c0001t0025 | 0/0 | 7281 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
a0001c0001t0026 | 0/0 | 7281 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
a0001c0001t0027 | 0/0 | 7281 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
a0001c0001t0028 | 0/0 | 7281 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
a0001c0001t0029 | 0/0 | 7282 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
a0001c0001t0030 | 0/0 | 7282 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
a0001c0001t0031 | 0/0 | 7281 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
a0001c0001t0032 | 0/0 | 7281 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
a0001c0001t0033 | 0/0 | 7281 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
a0001c0001t0034 | 0/0 | 7281 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
a0001c0001t0035 | 0/0 | 7281 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
a0001c0001t0036 | 0/0 | 7280 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
a0001c0001t0037 | 0/0 | 7281 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
a0001c0001t0038 | 0/0 | 7281 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | copy fasta | chr5 | 88712117 | 88888184 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0165 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0004g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0004g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0004g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0004g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0004g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0004g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0004g0115 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0004g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0004g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0004g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0004g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0004g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0004g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0005g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0005g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0005g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0006g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0006g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0006g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0006g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0006g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0007g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0007g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0007g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0007g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0007g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0008g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0008g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0008g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0008g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0008g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0009g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0009g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0009g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0009g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0010g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0010g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0010g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0011g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0011g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0011g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0012g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0012g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0012g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0013g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0013g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0013g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0014g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0014g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0015g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0015g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0016g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0016g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0017g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0018g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0019g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0020g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0021g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0022g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0023g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0024g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0025g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0026g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0027g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0028g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0029g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0030g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0031g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0032g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0033g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0034g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0035g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0036g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0037g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
a0001c0001t0038g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | GBR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0247 | EUR | GBR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG00280 | hp1 | a0001 | c0001 | t0004 | g0136 | EUR | FIN | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0168 | EUR | FIN | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG00323 | hp1 | a0001 | c0001 | t0004 | g0164 | EUR | FIN | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0139 | EUR | FIN | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | CHS | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG00597 | hp2 | a0001 | c0001 | t0013 | g0145 | EAS | CHS | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG00639 | hp1 | a0001 | c0001 | t0034 | g0012 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0252 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0248 | EAS | CHS | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG00673 | hp2 | a0001 | c0001 | t0013 | g0144 | EAS | CHS | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG00733 | hp1 | a0001 | c0001 | t0004 | g0080 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0255 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0261 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0292 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0169 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01081 | hp2 | a0001 | c0001 | t0004 | g0071 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01099 | hp1 | a0001 | c0001 | t0012 | g0057 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0266 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0237 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0113 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01192 | hp2 | a0001 | c0001 | t0004 | g0246 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01243 | hp1 | a0001 | c0001 | t0005 | g0013 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01243 | hp2 | a0001 | c0001 | t0004 | g0195 | AMR | PUR | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01255 | hp2 | a0001 | c0001 | t0012 | g0151 | AMR | CLM | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0245 | AMR | CLM | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0278 | AMR | CLM | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01361 | hp1 | a0001 | c0001 | t0004 | g0196 | AMR | CLM | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01433 | hp1 | a0001 | c0001 | t0008 | g0069 | AMR | CLM | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01433 | hp2 | a0001 | c0001 | t0012 | g0138 | AMR | CLM | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01496 | hp1 | a0001 | c0001 | t0004 | g0289 | AMR | CLM | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | CLM | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01515 | hp1 | a0001 | c0001 | t0010 | g0033 | EUR | IBS | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0173 | EUR | IBS | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01516 | hp1 | a0001 | c0001 | t0016 | g0074 | EUR | IBS | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0044 | EUR | IBS | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01517 | hp1 | a0001 | c0001 | t0010 | g0032 | EUR | IBS | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01517 | hp2 | a0001 | c0001 | t0016 | g0079 | EUR | IBS | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01884 | hp2 | a0001 | c0001 | t0004 | g0086 | AFR | ACB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0103 | AFR | ACB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01891 | hp2 | a0001 | c0001 | t0019 | g0067 | AFR | ACB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01928 | hp1 | a0001 | c0001 | t0009 | g0175 | AMR | PEL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0275 | AMR | PEL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0238 | AMR | PEL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01975 | hp1 | a0001 | c0001 | t0027 | g0263 | AMR | PEL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01975 | hp2 | a0001 | c0001 | t0008 | g0035 | AMR | PEL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01978 | hp2 | a0001 | c0001 | t0018 | g0119 | AMR | PEL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01981 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | PEL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01981 | hp2 | a0001 | c0001 | t0004 | g0011 | AMR | PEL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0270 | AMR | PEL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | KHV | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | KHV | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02040 | hp2 | a0001 | c0001 | t0013 | g0156 | EAS | KHV | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02055 | hp1 | a0001 | c0001 | t0035 | g0085 | AFR | ACB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02055 | hp2 | a0001 | c0001 | t0004 | g0208 | AFR | ACB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | KHV | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0293 | EAS | KHV | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | KHV | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | KHV | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0193 | AFR | ACB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | PEL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CDX | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02155 | hp2 | a0001 | c0001 | t0008 | g0068 | EAS | CDX | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0242 | AFR | ACB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0279 | AMR | PEL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0188 | AMR | PEL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0087 | AFR | ACB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0258 | AMR | PEL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02451 | hp1 | a0001 | c0001 | t0005 | g0084 | AFR | ACB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02451 | hp2 | a0001 | c0001 | t0004 | g0297 | AFR | ACB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | KHV | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02572 | hp1 | a0001 | c0001 | t0007 | g0300 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02572 | hp2 | a0001 | c0001 | t0029 | g0019 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0251 | SAS | PJL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02602 | hp2 | a0001 | c0001 | t0031 | g0167 | SAS | PJL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02615 | hp1 | a0001 | c0001 | t0036 | g0015 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0283 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02622 | hp1 | a0001 | c0001 | t0025 | g0153 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02622 | hp2 | a0001 | c0001 | t0004 | g0286 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02647 | hp1 | a0001 | c0001 | t0005 | g0298 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0231 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02683 | hp1 | a0001 | c0001 | t0038 | g0302 | SAS | PJL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0100 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02735 | hp1 | a0001 | c0001 | t0028 | g0170 | SAS | PJL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0046 | SAS | PJL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0182 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0099 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0194 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0287 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02896 | hp1 | a0001 | c0001 | t0007 | g0018 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02896 | hp2 | a0001 | c0001 | t0026 | g0037 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0288 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02897 | hp2 | a0001 | c0001 | t0007 | g0017 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0207 | AFR | ESN | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02922 | hp2 | a0001 | c0001 | t0014 | g0295 | AFR | ESN | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0098 | AFR | ESN | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0217 | AFR | ESN | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02970 | hp1 | a0001 | c0001 | t0005 | g0083 | AFR | ESN | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02970 | hp2 | a0001 | c0001 | t0014 | g0290 | AFR | ESN | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0091 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG03098 | hp1 | a0001 | c0001 | t0015 | g0081 | AFR | MSL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG03098 | hp2 | a0001 | c0001 | t0004 | g0082 | AFR | MSL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | ESN | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0256 | AFR | ESN | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0185 | AFR | ESN | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0243 | AFR | MSL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG03209 | hp2 | a0001 | c0001 | t0004 | g0088 | AFR | MSL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0191 | AFR | MSL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG03225 | hp2 | a0001 | c0001 | t0024 | g0066 | AFR | MSL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0216 | SAS | PJL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG03540 | hp1 | a0001 | c0001 | t0004 | g0285 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0232 | AFR | MSL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG03579 | hp2 | a0001 | c0001 | t0004 | g0284 | AFR | MSL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0234 | SAS | PJL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG03669 | hp2 | a0001 | c0001 | t0004 | g0112 | SAS | PJL | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0049 | SAS | STU | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG03688 | hp2 | a0001 | c0001 | t0004 | g0111 | SAS | STU | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | BEB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0027 | SAS | BEB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG03942 | hp1 | a0001 | c0001 | t0037 | g0236 | SAS | BEB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0045 | SAS | BEB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0249 | SAS | STU | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0034 | SAS | STU | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0199 | SAS | BEB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | STU | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0235 | SAS | STU | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | STU | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0026 | SAS | STU | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | YRI | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18522 | hp2 | a0001 | c0001 | t0015 | g0089 | AFR | YRI | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | CHB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | CHB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | YRI | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18906 | hp2 | a0001 | c0001 | t0030 | g0109 | AFR | YRI | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18941 | hp1 | a0001 | c0001 | t0006 | g0150 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18945 | hp1 | a0001 | c0001 | t0006 | g0149 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18945 | hp2 | a0001 | c0001 | t0022 | g0211 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18949 | hp1 | a0001 | c0001 | t0003 | g0282 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0277 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0269 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18966 | hp2 | a0001 | c0001 | t0009 | g0178 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18967 | hp1 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18969 | hp2 | a0001 | c0001 | t0009 | g0179 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18970 | hp1 | a0001 | c0001 | t0006 | g0134 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0299 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18979 | hp2 | a0001 | c0001 | t0021 | g0197 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18980 | hp1 | a0001 | c0001 | t0006 | g0133 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18982 | hp2 | a0001 | c0001 | t0011 | g0055 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18992 | hp1 | a0001 | c0001 | t0011 | g0053 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18992 | hp2 | a0001 | c0001 | t0003 | g0264 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0294 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0296 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19009 | hp2 | a0001 | c0001 | t0023 | g0209 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19010 | hp1 | a0001 | c0001 | t0006 | g0148 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0276 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19011 | hp2 | a0001 | c0001 | t0009 | g0177 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0239 | AFR | LWK | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19030 | hp2 | a0001 | c0001 | t0004 | g0108 | AFR | LWK | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0192 | AFR | LWK | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0076 | AFR | LWK | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19056 | hp1 | a0001 | c0001 | t0017 | g0253 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19063 | hp1 | a0001 | c0001 | t0003 | g0265 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19077 | hp1 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19082 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0272 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19084 | hp2 | a0001 | c0001 | t0008 | g0107 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19086 | hp1 | a0001 | c0001 | t0003 | g0271 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19086 | hp2 | a0001 | c0001 | t0011 | g0054 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19091 | hp1 | a0001 | c0001 | t0008 | g0184 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0127 | AFR | YRI | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA19240 | hp2 | a0001 | c0001 | t0007 | g0301 | AFR | YRI | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA20129 | hp1 | a0001 | c0001 | t0033 | g0060 | AFR | ASW | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | ASW | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA20752 | hp1 | a0001 | c0001 | t0004 | g0114 | EUR | TSI | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0010 | EUR | TSI | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0250 | SAS | GIH | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA20905 | hp2 | a0001 | c0001 | t0010 | g0056 | SAS | GIH | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | CLM | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | ACB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0230 | AFR | ACB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02559 | hp1 | a0001 | c0001 | t0004 | g0291 | AFR | ACB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG02559 | hp2 | a0001 | c0001 | t0005 | g0014 | AFR | ACB | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | USA | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
HG06807 | hp2 | a0001 | c0001 | t0007 | g0016 | AFR | USA | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA18955 | hp2 | a0001 | c0001 | t0032 | g0130 | EAS | JPT | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA21309 | hp1 | a0001 | c0001 | t0020 | g0004 | AFR | LWK | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0244 | AFR | LWK | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0115 | REF | REF | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0165 | REF | REF | MEF2C_chr5_88712117_88888184 | MEF2C | chr5 | 88712117 | 88888184 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:88823930
|
G | T | 1 | a0001 | 1 | NA19056.hp1 | splice_region_variant | LOW | c.-142C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/11 | chr5 | 88823930 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:88717390
|
T | C | 2 | a0001c0001t0006a0001c0001t0009 | 9 | HG01928.hp1 NA18941.hp1 NA18945.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5214A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 5214 | chr5 | 88717390 | |||||
chr5:88717417
|
T | G | 1 | a0001c0001t0020 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5187A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 5187 | chr5 | 88717417 | |||||
chr5:88717769
|
C | G | 1 | a0001c0001t0012 | 3 | HG01099.hp1 HG01255.hp2 HG01433.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4835G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 4835 | chr5 | 88717769 | |||||
chr5:88717994
|
A | G | 1 | a0001c0001t0026 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4610T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 4610 | chr5 | 88717994 | |||||
chr5:88718056
|
G | A | 7 | a0001c0001t0005a0001c0001t0007a0001c0001t0015others(4): Show | 16 | HG00639.hp1 HG01243.hp1 HG02451.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*4548C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 4548 | chr5 | 88718056 | |||||
chr5:88718621
|
C | T | 1 | a0001c0001t0022 | 1 | NA18945.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3983G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 3983 | chr5 | 88718621 | |||||
chr5:88718706
|
A | G | 1 | a0001c0001t0016 | 2 | HG01516.hp1 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3898T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 3898 | chr5 | 88718706 | |||||
chr5:88719016
|
T | C | 1 | a0001c0001t0030 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3588A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 3588 | chr5 | 88719016 | |||||
chr5:88719021
|
T | G | 1 | a0001c0001t0033 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3583A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 3583 | chr5 | 88719021 | |||||
chr5:88719140
|
T | C | 1 | a0001c0001t0034 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3464A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 3464 | chr5 | 88719140 | |||||
chr5:88719385
|
T | C | 1 | a0001c0001t0011 | 3 | NA18982.hp2 NA18992.hp1 NA19086.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3219A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 3219 | chr5 | 88719385 | |||||
chr5:88719477
|
C | T | 1 | a0001c0001t0014 | 2 | HG02922.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3127G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 3127 | chr5 | 88719477 | |||||
chr5:88719490
|
C | T | 1 | a0001c0001t0032 | 1 | NA18955.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3114G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 3114 | chr5 | 88719490 | |||||
chr5:88719491
|
G | A | 1 | a0001c0001t0023 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3113C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 3113 | chr5 | 88719491 | |||||
chr5:88719726
|
C | T | 1 | a0001c0001t0021 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2878G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 2878 | chr5 | 88719726 | |||||
chr5:88719728
|
A | C | 20 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(17): Show | 117 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*2876T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 2876 | chr5 | 88719728 | |||||
chr5:88719966
|
T | C | 1 | a0001c0001t0027 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2638A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 2638 | chr5 | 88719966 | |||||
chr5:88720059
|
A | G | 1 | a0001c0001t0031 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2545T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 2545 | chr5 | 88720059 | |||||
chr5:88720191
|
A | G | 29 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(26): Show | 205 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*2413T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 2413 | chr5 | 88720191 | |||||
chr5:88720214
|
G | A | 1 | a0001c0001t0013 | 3 | HG00597.hp2 HG00673.hp2 HG02040.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2390C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 2390 | chr5 | 88720214 | |||||
chr5:88720237
|
T | A | 1 | a0001c0001t0035 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2367A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 2367 | chr5 | 88720237 | |||||
chr5:88720336
|
A | AT | 24 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(21): Show | 194 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(191): Show |
3_prime_UTR_variant | MODIFIER | c.*2267dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 2267 | chr5 | 88720336 | |||||
chr5:88720336
|
A | ATT | 4 | a0001c0001t0010a0001c0001t0015a0001c0001t0029others(1): Show | 7 | HG01515.hp1 HG01517.hp1 HG02572.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2266_*2267dupAA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 2267 | chr5 | 88720336 | |||||
chr5:88720546
|
A | T | 1 | a0001c0001t0028 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2058T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 2058 | chr5 | 88720546 | |||||
chr5:88720708
|
T | C | 1 | a0001c0001t0037 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1896A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 1896 | chr5 | 88720708 | |||||
chr5:88720787
|
AT | A | 20 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(17): Show | 117 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*1816delA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 1816 | chr5 | 88720787 | |||||
chr5:88721798
|
T | C | 1 | a0001c0001t0008 | 5 | HG01433.hp1 HG01975.hp2 HG02155.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*806A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 806 | chr5 | 88721798 | |||||
chr5:88722571
|
GA | G | 6 | a0001c0001t0004a0001c0001t0005a0001c0001t0014others(3): Show | 46 | HG00280.hp1 HG00323.hp1 HG00733.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*32delT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 32 | chr5 | 88722571 | |||||
chr5:88722575
|
A | G | 1 | a0001c0001t0018 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*29T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 11/11 | 29 | chr5 | 88722575 | |||||
chr5:88883019
|
G | A | 1 | a0001c0001t0038 | 1 | HG02683.hp1 | 5_prime_UTR_variant | MODIFIER | c.-207C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/11 | 59231 | chr5 | 88883019 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:88723063
|
C | A | 1 | a0001c0001t0001g0090 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1101-138G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88723063 | ||||||
chr5:88723179
|
G | A | 2 | a0001c0001t0029g0019a0001c0001t0030g0109 | 2 | HG02572.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1101-254C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88723179 | ||||||
chr5:88723576
|
C | T | 2 | a0001c0001t0014g0290a0001c0001t0014g0295 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1101-651G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88723576 | ||||||
chr5:88723657
|
G | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(95): Show | 98 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.1101-732C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88723657 | ||||||
chr5:88723720
|
G | A | 1 | a0001c0001t0012g0138 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1101-795C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88723720 | ||||||
chr5:88723746
|
T | C | 1 | a0001c0001t0023g0209 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1101-821A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88723746 | ||||||
chr5:88723812
|
T | C | 97 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(94): Show | 97 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.1101-887A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88723812 | ||||||
chr5:88723930
|
G | C | 97 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(94): Show | 97 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.1101-1005C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88723930 | ||||||
chr5:88724059
|
A | G | 1 | a0001c0001t0024g0066 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1101-1134T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88724059 | ||||||
chr5:88724205
|
G | T | 1 | a0001c0001t0001g0140 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1101-1280C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88724205 | ||||||
chr5:88724364
|
C | T | 3 | a0001c0001t0004g0108a0001c0001t0029g0019a0001c0001t0030g0109 | 3 | HG02572.hp2 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1101-1439G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88724364 | ||||||
chr5:88724502
|
C | G | 97 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(94): Show | 97 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.1101-1577G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88724502 | ||||||
chr5:88724528
|
T | C | 1 | a0001c0001t0003g0250 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1101-1603A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88724528 | ||||||
chr5:88724574
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1101-1649A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88724574 | ||||||
chr5:88725017
|
A | G | 9 | a0001c0001t0001g0065a0001c0001t0002g0026a0001c0001t0002g0027others(6): Show | 9 | HG01515.hp1 HG01517.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.1101-2092T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88725017 | ||||||
chr5:88725193
|
T | C | 2 | a0001c0001t0001g0129a0001c0001t0001g0190 | 2 | NA18998.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1101-2268A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88725193 | ||||||
chr5:88725494
|
G | A | 1 | a0001c0001t0004g0114 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1101-2569C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88725494 | ||||||
chr5:88725512
|
C | T | 1 | a0001c0001t0013g0144 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1101-2587G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88725512 | ||||||
chr5:88725535
|
T | C | 2 | a0001c0001t0015g0081a0001c0001t0015g0089 | 2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1101-2610A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88725535 | ||||||
chr5:88725574
|
G | A | 24 | a0001c0001t0004g0011a0001c0001t0004g0082a0001c0001t0004g0086others(21): Show | 24 | HG01192.hp2 HG01496.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.1101-2649C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88725574 | ||||||
chr5:88725710
|
T | G | 97 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(94): Show | 97 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.1100+2783A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88725710 | ||||||
chr5:88725905
|
G | A | 6 | a0001c0001t0004g0011a0001c0001t0004g0111a0001c0001t0004g0112others(3): Show | 6 | HG01192.hp2 HG01981.hp2 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.1100+2588C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88725905 | ||||||
chr5:88725982
|
T | C | 2 | a0001c0001t0001g0039a0001c0001t0001g0273 | 2 | NA18959.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1100+2511A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88725982 | ||||||
chr5:88726001
|
T | C | 2 | a0001c0001t0001g0135a0001c0001t0001g0166 | 2 | HG01070.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1100+2492A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88726001 | ||||||
chr5:88726515
|
G | A | 3 | a0001c0001t0004g0108a0001c0001t0029g0019a0001c0001t0030g0109 | 3 | HG02572.hp2 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1100+1978C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88726515 | ||||||
chr5:88726562
|
G | A | 3 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0045 | 3 | HG03834.hp2 HG03942.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1100+1931C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88726562 | ||||||
chr5:88726733
|
CTGTCCCT others(4): Show |
C | 3 | a0001c0001t0002g0048a0001c0001t0003g0041a0001c0001t0003g0051 | 3 | NA18955.hp1 NA18966.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1100+1749_1100+175 others(15): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88726733 | ||||||
chr5:88727323
|
T | A | 1 | a0001c0001t0001g0120 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1100+1170A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88727323 | ||||||
chr5:88727339
|
A | T | 1 | a0001c0001t0001g0120 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1100+1154T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88727339 | ||||||
chr5:88727349
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1100+1144C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88727349 | ||||||
chr5:88727532
|
A | T | 107 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(104): Show | 107 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.1100+961T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88727532 | ||||||
chr5:88727758
|
G | A | 1 | a0001c0001t0001g0001 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1100+735C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88727758 | ||||||
chr5:88727805
|
GA | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(105): Show | 108 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.1100+687delT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88727805 | ||||||
chr5:88728382
|
A | G | 2 | a0001c0001t0004g0195a0001c0001t0004g0196 | 2 | HG01243.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1100+111T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 10/10 | chr5 | 88728382 | ||||||
chr5:88729055
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.964+163C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 9/10 | chr5 | 88729055 | ||||||
chr5:88729195
|
T | C | 2 | a0001c0001t0001g0126a0001c0001t0001g0154 | 2 | NA19001.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.964+23A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 9/10 | chr5 | 88729195 | ||||||
chr5:88729373
|
A | C | 1 | a0001c0001t0001g0008 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.835-26T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 8/10 | chr5 | 88729373 | ||||||
chr5:88729940
|
A | G | 1 | a0001c0001t0037g0236 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.834+271T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 8/10 | chr5 | 88729940 | ||||||
chr5:88730005
|
T | G | 1 | a0001c0001t0002g0070 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.834+206A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 8/10 | chr5 | 88730005 | ||||||
chr5:88730028
|
CA | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.834+182delT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 8/10 | chr5 | 88730028 | ||||||
chr5:88730196
|
G | A | 2 | a0001c0001t0004g0108a0001c0001t0030g0109 | 2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.834+15C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 8/10 | chr5 | 88730196 | ||||||
chr5:88730328
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.811-94A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 7/10 | chr5 | 88730328 | ||||||
chr5:88730362
|
A | G | 1 | a0001c0001t0033g0060 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.811-128T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 7/10 | chr5 | 88730362 | ||||||
chr5:88730524
|
A | G | 6 | a0001c0001t0004g0082a0001c0001t0004g0086a0001c0001t0004g0087others(3): Show | 6 | HG01496.hp1 HG01884.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.811-290T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 7/10 | chr5 | 88730524 | ||||||
chr5:88730645
|
G | C | 1 | a0001c0001t0021g0197 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.811-411C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 7/10 | chr5 | 88730645 | ||||||
chr5:88730850
|
A | G | 2 | a0001c0001t0004g0285a0001c0001t0004g0289 | 2 | HG01496.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.811-616T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 7/10 | chr5 | 88730850 | ||||||
chr5:88730995
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.810+734G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 7/10 | chr5 | 88730995 | ||||||
chr5:88731051
|
A | C | 6 | a0001c0001t0005g0013a0001c0001t0005g0014a0001c0001t0005g0083others(3): Show | 6 | HG01243.hp1 HG02451.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.810+678T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 7/10 | chr5 | 88731051 | ||||||
chr5:88731053
|
C | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(105): Show | 108 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.810+676G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 7/10 | chr5 | 88731053 | ||||||
chr5:88731085
|
C | T | 132 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(129): Show | 132 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.810+644G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 7/10 | chr5 | 88731085 | ||||||
chr5:88731232
|
G | A | 1 | a0001c0001t0003g0255 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.810+497C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 7/10 | chr5 | 88731232 | ||||||
chr5:88731243
|
A | C | 2 | a0001c0001t0015g0081a0001c0001t0015g0089 | 2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.810+486T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 7/10 | chr5 | 88731243 | ||||||
chr5:88731332
|
G | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(105): Show | 108 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.810+397C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 7/10 | chr5 | 88731332 | ||||||
chr5:88731400
|
T | C | 69 | a0001c0001t0001g0065a0001c0001t0002g0007a0001c0001t0002g0021others(66): Show | 69 | HG00597.hp1 HG01433.hp1 HG01515.hp1 others(66): Show |
intron_variant | MODIFIER | c.810+329A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 7/10 | chr5 | 88731400 | ||||||
chr5:88731461
|
G | A | 4 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(1): Show | 4 | HG01168.hp2 HG01169.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.810+268C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 7/10 | chr5 | 88731461 | ||||||
chr5:88731525
|
T | C | 2 | a0001c0001t0006g0148a0001c0001t0006g0149 | 2 | NA18945.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.810+204A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 7/10 | chr5 | 88731525 | ||||||
chr5:88731530
|
A | AT | 25 | a0001c0001t0001g0075a0001c0001t0002g0020a0001c0001t0002g0034others(22): Show | 25 | HG00280.hp1 HG00323.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.810+198dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 7/10 | chr5 | 88731530 | ||||||
chr5:88731530
|
A | T | 20 | a0001c0001t0004g0082a0001c0001t0004g0086a0001c0001t0004g0087others(17): Show | 20 | HG01496.hp1 HG01884.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.810+199T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 7/10 | chr5 | 88731530 | ||||||
chr5:88731970
|
A | G | 1 | a0001c0001t0010g0056 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.638-69T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88731970 | ||||||
chr5:88732476
|
A | T | 2 | a0001c0001t0001g0008a0001c0001t0002g0003 | 2 | HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.638-575T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88732476 | ||||||
chr5:88732477
|
G | T | 2 | a0001c0001t0001g0104a0001c0001t0001g0105 | 2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.638-576C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88732477 | ||||||
chr5:88732637
|
T | A | 1 | a0001c0001t0020g0004 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.638-736A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88732637 | ||||||
chr5:88732667
|
A | T | 1 | a0001c0001t0021g0197 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.638-766T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88732667 | ||||||
chr5:88732820
|
G | C | 1 | a0001c0001t0035g0085 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.638-919C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88732820 | ||||||
chr5:88732994
|
G | T | 1 | a0001c0001t0001g0273 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.638-1093C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88732994 | ||||||
chr5:88733023
|
C | T | 2 | a0001c0001t0019g0067a0001c0001t0024g0066 | 2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.638-1122G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88733023 | ||||||
chr5:88733167
|
G | A | 4 | a0001c0001t0002g0200a0001c0001t0002g0201a0001c0001t0002g0202others(1): Show | 4 | NA18951.hp2 NA18969.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.638-1266C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88733167 | ||||||
chr5:88733257
|
T | C | 5 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220others(2): Show | 5 | NA18949.hp2 NA18965.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.638-1356A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88733257 | ||||||
chr5:88733391
|
T | C | 2 | a0001c0001t0002g0044a0001c0001t0002g0174 | 2 | HG01069.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.638-1490A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88733391 | ||||||
chr5:88733700
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.638-1799T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88733700 | ||||||
chr5:88733810
|
C | T | 211 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(208): Show | 211 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.638-1909G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88733810 | ||||||
chr5:88733890
|
A | G | 2 | a0001c0001t0019g0067a0001c0001t0024g0066 | 2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.638-1989T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88733890 | ||||||
chr5:88733936
|
C | T | 1 | a0001c0001t0020g0004 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.638-2035G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88733936 | ||||||
chr5:88734013
|
C | T | 1 | a0001c0001t0003g0233 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.638-2112G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734013 | ||||||
chr5:88734037
|
C | A | 1 | a0001c0001t0034g0012 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.638-2136G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734037 | ||||||
chr5:88734208
|
A | G | 2 | a0001c0001t0005g0013a0001c0001t0005g0014 | 2 | HG01243.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.638-2307T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734208 | ||||||
chr5:88734475
|
G | A | 1 | a0001c0001t0002g0021 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.638-2574C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734475 | ||||||
chr5:88734479
|
C | T | 1 | a0001c0001t0003g0091 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.638-2578G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734479 | ||||||
chr5:88734561
|
G | GT | 3 | a0001c0001t0004g0284a0001c0001t0004g0287a0001c0001t0015g0089 | 3 | HG02895.hp2 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.638-2661dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734561 | ||||||
chr5:88734561
|
G | T | 1 | a0001c0001t0004g0164 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.638-2660C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734561 | ||||||
chr5:88734561
|
GTTTGTTT others(10): Show |
G | 3 | a0001c0001t0002g0073a0001c0001t0016g0074a0001c0001t0016g0079 | 3 | HG01169.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.638-2677_638-2661d others(19): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734561 | ||||||
chr5:88734565
|
G | GT | 27 | a0001c0001t0001g0267a0001c0001t0001g0273a0001c0001t0003g0041others(24): Show | 27 | HG00642.hp1 HG01192.hp1 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.638-2665dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734565 | ||||||
chr5:88734565
|
G | GTTTTTTT others(3): Show |
3 | a0001c0001t0002g0046a0001c0001t0004g0080a0001c0001t0030g0109 | 3 | HG00733.hp1 HG02735.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.638-2674_638-2665d others(12): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734565 | ||||||
chr5:88734565
|
G | GTTTTTTT others(4): Show |
4 | a0001c0001t0002g0050a0001c0001t0002g0102a0001c0001t0002g0132others(1): Show | 4 | HG01496.hp2 NA18982.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.638-2675_638-2665d others(13): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734565 | ||||||
chr5:88734565
|
G | GTTTTTTT others(5): Show |
3 | a0001c0001t0002g0047a0001c0001t0011g0053a0001c0001t0011g0054 | 3 | HG03490.hp1 NA18992.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.638-2676_638-2665d others(14): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734565 | ||||||
chr5:88734565
|
G | GTTTTTTT others(6): Show |
1 | a0001c0001t0002g0162 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.638-2677_638-2665d others(15): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734565 | ||||||
chr5:88734565
|
G | T | 9 | a0001c0001t0004g0099a0001c0001t0004g0136a0001c0001t0004g0164others(6): Show | 9 | HG00280.hp1 HG00323.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.638-2664C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734565 | ||||||
chr5:88734565
|
GTTTTT | G | 16 | a0001c0001t0001g0008a0001c0001t0001g0058a0001c0001t0001g0078others(13): Show | 16 | HG00673.hp2 HG01361.hp2 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.638-2669_638-2665d others(7): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734565 | ||||||
chr5:88734565
|
GTTTTTT | G | 86 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0022others(83): Show | 86 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.638-2670_638-2665d others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734565 | ||||||
chr5:88734565
|
GTTTTTTT others(13): Show |
G | 1 | a0001c0001t0003g0242 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.638-2684_638-2665d others(22): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734565 | ||||||
chr5:88734567
|
T | TTTTTTTT others(4): Show |
1 | a0001c0001t0002g0049 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.638-2667_638-2666i others(13): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734567 | ||||||
chr5:88734568
|
T | G | 1 | a0001c0001t0003g0237 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.638-2667A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734568 | ||||||
chr5:88734574
|
T | TTG | 11 | a0001c0001t0002g0062a0001c0001t0002g0182a0001c0001t0002g0183others(8): Show | 11 | HG00597.hp1 HG02145.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.638-2674_638-2673i others(4): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734574 | ||||||
chr5:88734575
|
T | G | 1 | a0001c0001t0003g0248 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.638-2674A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734575 | ||||||
chr5:88734575
|
T | TG | 54 | a0001c0001t0001g0065a0001c0001t0002g0007a0001c0001t0002g0021others(51): Show | 54 | HG01433.hp1 HG02015.hp2 HG02027.hp1 others(51): Show |
intron_variant | MODIFIER | c.638-2675_638-2674i others(3): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734575 | ||||||
chr5:88734576
|
T | G | 4 | a0001c0001t0008g0035a0001c0001t0010g0032a0001c0001t0010g0033others(1): Show | 4 | HG01515.hp1 HG01517.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.638-2675A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734576 | ||||||
chr5:88734579
|
T | G | 1 | a0001c0001t0003g0240 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.638-2678A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734579 | ||||||
chr5:88734580
|
T | G | 4 | a0001c0001t0005g0013a0001c0001t0005g0014a0001c0001t0005g0298others(1): Show | 4 | HG01243.hp1 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.638-2679A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734580 | ||||||
chr5:88734581
|
T | G | 1 | a0001c0001t0003g0250 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.638-2680A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734581 | ||||||
chr5:88734582
|
T | G | 1 | a0001c0001t0001g0155 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.638-2681A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734582 | ||||||
chr5:88734585
|
T | G | 4 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0045others(1): Show | 4 | HG00673.hp1 HG03834.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.638-2684A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734585 | ||||||
chr5:88734587
|
T | G | 2 | a0001c0001t0005g0083a0001c0001t0005g0084 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.638-2686A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734587 | ||||||
chr5:88734588
|
T | G | 1 | a0001c0001t0001g0038 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.638-2687A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734588 | ||||||
chr5:88734853
|
C | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.638-2952G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88734853 | ||||||
chr5:88735119
|
A | G | 1 | a0001c0001t0003g0255 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.638-3218T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88735119 | ||||||
chr5:88735182
|
G | A | 1 | a0001c0001t0002g0268 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.638-3281C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88735182 | ||||||
chr5:88735294
|
G | A | 1 | a0001c0001t0036g0015 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.638-3393C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88735294 | ||||||
chr5:88735324
|
T | C | 1 | a0001c0001t0004g0256 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.638-3423A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88735324 | ||||||
chr5:88735498
|
T | C | 1 | a0001c0001t0021g0197 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.638-3597A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88735498 | ||||||
chr5:88735734
|
C | G | 1 | a0001c0001t0002g0213 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.638-3833G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88735734 | ||||||
chr5:88735856
|
T | G | 1 | a0001c0001t0001g0181 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.638-3955A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88735856 | ||||||
chr5:88735857
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.638-3956G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88735857 | ||||||
chr5:88735921
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.638-4020G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88735921 | ||||||
chr5:88735960
|
A | G | 2 | a0001c0001t0001g0104a0001c0001t0001g0105 | 2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.638-4059T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88735960 | ||||||
chr5:88735965
|
A | C | 3 | a0001c0001t0004g0108a0001c0001t0029g0019a0001c0001t0030g0109 | 3 | HG02572.hp2 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.638-4064T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88735965 | ||||||
chr5:88736003
|
T | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(105): Show | 108 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.638-4102A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88736003 | ||||||
chr5:88736195
|
TAAATATT others(323): Show |
T | 210 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(207): Show | 210 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.638-4624_638-4295d others(2): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88736195 | ||||||
chr5:88736356
|
C | T | 1 | a0001c0001t0004g0239 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.638-4455G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88736356 | ||||||
chr5:88736360
|
G | T | 1 | a0001c0001t0004g0239 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.638-4459C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88736360 | ||||||
chr5:88736363
|
G | A | 2 | a0001c0001t0019g0067a0001c0001t0024g0066 | 2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.638-4462C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88736363 | ||||||
chr5:88736500
|
C | CA | 14 | a0001c0001t0001g0267a0001c0001t0001g0273a0001c0001t0002g0048others(11): Show | 14 | HG01361.hp1 HG01891.hp2 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.638-4600dupT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88736500 | ||||||
chr5:88736621
|
C | T | 1 | a0001c0001t0001g0092 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.638-4720G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88736621 | ||||||
chr5:88736705
|
C | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(105): Show | 108 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.638-4804G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88736705 | ||||||
chr5:88736834
|
G | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(105): Show | 108 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.638-4933C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88736834 | ||||||
chr5:88736903
|
T | C | 1 | a0001c0001t0007g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.638-5002A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88736903 | ||||||
chr5:88737059
|
A | T | 2 | a0001c0001t0011g0053a0001c0001t0011g0054 | 2 | NA18992.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.638-5158T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88737059 | ||||||
chr5:88737284
|
T | C | 69 | a0001c0001t0001g0065a0001c0001t0002g0007a0001c0001t0002g0021others(66): Show | 69 | HG00597.hp1 HG01433.hp1 HG01515.hp1 others(66): Show |
intron_variant | MODIFIER | c.638-5383A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88737284 | ||||||
chr5:88737304
|
G | A | 1 | a0001c0001t0010g0056 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.638-5403C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88737304 | ||||||
chr5:88737512
|
C | A | 3 | a0001c0001t0004g0108a0001c0001t0029g0019a0001c0001t0030g0109 | 3 | HG02572.hp2 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.638-5611G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88737512 | ||||||
chr5:88737677
|
A | G | 2 | a0001c0001t0002g0224a0001c0001t0002g0225 | 2 | NA18944.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.638-5776T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88737677 | ||||||
chr5:88737773
|
G | A | 2 | a0001c0001t0019g0067a0001c0001t0024g0066 | 2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.638-5872C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88737773 | ||||||
chr5:88737805
|
C | A | 1 | a0001c0001t0001g0181 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.638-5904G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88737805 | ||||||
chr5:88738013
|
G | C | 1 | a0001c0001t0015g0089 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.638-6112C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88738013 | ||||||
chr5:88738052
|
G | C | 1 | a0001c0001t0004g0239 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.638-6151C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88738052 | ||||||
chr5:88738333
|
G | A | 1 | a0001c0001t0007g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.638-6432C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88738333 | ||||||
chr5:88738376
|
T | C | 1 | a0001c0001t0004g0098 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.638-6475A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88738376 | ||||||
chr5:88738447
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.638-6546T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88738447 | ||||||
chr5:88738646
|
T | G | 1 | a0001c0001t0001g0147 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.638-6745A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88738646 | ||||||
chr5:88738815
|
C | G | 1 | a0001c0001t0001g0147 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.638-6914G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88738815 | ||||||
chr5:88739000
|
G | C | 1 | a0001c0001t0007g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.638-7099C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88739000 | ||||||
chr5:88739050
|
T | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(207): Show | 210 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.638-7149A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88739050 | ||||||
chr5:88739251
|
A | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(209): Show | 212 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.638-7350T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88739251 | ||||||
chr5:88739611
|
T | A | 1 | a0001c0001t0020g0004 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.638-7710A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88739611 | ||||||
chr5:88739715
|
A | T | 6 | a0001c0001t0001g0031a0001c0001t0001g0052a0001c0001t0003g0010others(3): Show | 6 | HG01099.hp1 HG01255.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.638-7814T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88739715 | ||||||
chr5:88740024
|
G | A | 2 | a0001c0001t0014g0290a0001c0001t0014g0295 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.638-8123C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88740024 | ||||||
chr5:88740070
|
C | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(105): Show | 108 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.638-8169G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88740070 | ||||||
chr5:88740199
|
C | T | 1 | a0001c0001t0037g0236 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.638-8298G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88740199 | ||||||
chr5:88740233
|
C | CGT | 87 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(84): Show | 87 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.638-8334_638-8333d others(4): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88740233 | ||||||
chr5:88740233
|
C | CGTGT | 23 | a0001c0001t0001g0038a0001c0001t0001g0077a0001c0001t0001g0104others(20): Show | 23 | HG00323.hp1 HG00597.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.638-8336_638-8333d others(6): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88740233 | ||||||
chr5:88740233
|
C | CGTGTGT | 47 | a0001c0001t0001g0065a0001c0001t0001g0075a0001c0001t0002g0021others(44): Show | 47 | HG00597.hp1 HG01081.hp2 HG01433.hp1 others(44): Show |
intron_variant | MODIFIER | c.638-8338_638-8333d others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88740233 | ||||||
chr5:88740233
|
C | CGTGTGTG others(1): Show |
14 | a0001c0001t0001g0090a0001c0001t0001g0125a0001c0001t0002g0007others(11): Show | 14 | HG01884.hp1 HG02015.hp2 HG02129.hp2 others(11): Show |
intron_variant | MODIFIER | c.638-8340_638-8333d others(10): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88740233 | ||||||
chr5:88740233
|
C | CGTGTGTG others(3): Show |
8 | a0001c0001t0001g0126a0001c0001t0001g0154a0001c0001t0002g0030others(5): Show | 8 | HG02145.hp2 HG02965.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.638-8342_638-8333d others(12): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88740233 | ||||||
chr5:88740233
|
C | CGTGTGTG others(5): Show |
1 | a0001c0001t0035g0085 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.638-8344_638-8333d others(14): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88740233 | ||||||
chr5:88740233
|
CGT | C | 88 | a0001c0001t0001g0267a0001c0001t0002g0020a0001c0001t0002g0048others(85): Show | 88 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.638-8334_638-8333d others(4): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88740233 | ||||||
chr5:88740233
|
CGTGT | C | 4 | a0001c0001t0001g0008a0001c0001t0003g0233a0001c0001t0004g0011others(1): Show | 4 | HG01981.hp2 HG02135.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.638-8336_638-8333d others(6): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88740233 | ||||||
chr5:88740233
|
CGTGTGTG others(7): Show |
C | 1 | a0001c0001t0001g0273 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.638-8346_638-8333d others(16): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88740233 | ||||||
chr5:88740407
|
T | C | 1 | a0001c0001t0002g0216 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.638-8506A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88740407 | ||||||
chr5:88740516
|
G | A | 4 | a0001c0001t0007g0017a0001c0001t0007g0018a0001c0001t0007g0300others(1): Show | 4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.637+8554C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88740516 | ||||||
chr5:88740669
|
C | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.637+8401G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88740669 | ||||||
chr5:88740691
|
A | C | 7 | a0001c0001t0001g0031a0001c0001t0001g0052a0001c0001t0001g0110others(4): Show | 7 | HG00639.hp2 HG01099.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.637+8379T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88740691 | ||||||
chr5:88740763
|
T | C | 2 | a0001c0001t0009g0178a0001c0001t0009g0179 | 2 | NA18966.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.637+8307A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88740763 | ||||||
chr5:88740964
|
A | G | 1 | a0001c0001t0025g0153 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.637+8106T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88740964 | ||||||
chr5:88741060
|
C | T | 1 | a0001c0001t0007g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.637+8010G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88741060 | ||||||
chr5:88741107
|
C | T | 1 | a0001c0001t0034g0012 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.637+7963G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88741107 | ||||||
chr5:88741160
|
G | A | 1 | a0001c0001t0003g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.637+7910C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88741160 | ||||||
chr5:88741206
|
G | A | 1 | a0001c0001t0008g0069 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.637+7864C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88741206 | ||||||
chr5:88741339
|
T | A | 2 | a0001c0001t0005g0083a0001c0001t0005g0084 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.637+7731A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88741339 | ||||||
chr5:88741392
|
T | A | 12 | a0001c0001t0003g0113a0001c0001t0003g0169a0001c0001t0003g0233others(9): Show | 12 | HG00099.hp2 HG00642.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.637+7678A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88741392 | ||||||
chr5:88741481
|
C | T | 1 | a0001c0001t0001g0024 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.637+7589G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88741481 | ||||||
chr5:88741997
|
T | G | 1 | a0001c0001t0007g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.637+7073A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88741997 | ||||||
chr5:88742160
|
G | C | 2 | a0001c0001t0015g0081a0001c0001t0015g0089 | 2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.637+6910C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88742160 | ||||||
chr5:88742558
|
T | A | 4 | a0001c0001t0007g0017a0001c0001t0007g0018a0001c0001t0007g0300others(1): Show | 4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.637+6512A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88742558 | ||||||
chr5:88742573
|
A | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.637+6497T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88742573 | ||||||
chr5:88742903
|
T | C | 1 | a0001c0001t0001g0228 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.637+6167A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88742903 | ||||||
chr5:88742949
|
A | C | 1 | a0001c0001t0026g0037 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.637+6121T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88742949 | ||||||
chr5:88743028
|
C | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(105): Show | 108 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.637+6042G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88743028 | ||||||
chr5:88743141
|
A | T | 1 | a0001c0001t0007g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.637+5929T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88743141 | ||||||
chr5:88743308
|
C | G | 1 | a0001c0001t0002g0243 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.637+5762G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88743308 | ||||||
chr5:88743421
|
A | G | 2 | a0001c0001t0002g0102a0001c0001t0002g0132 | 2 | NA19065.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.637+5649T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88743421 | ||||||
chr5:88743578
|
C | G | 1 | a0001c0001t0002g0192 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.637+5492G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88743578 | ||||||
chr5:88743689
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.637+5381C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88743689 | ||||||
chr5:88743843
|
T | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.637+5227A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88743843 | ||||||
chr5:88743898
|
C | T | 1 | a0001c0001t0007g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.637+5172G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88743898 | ||||||
chr5:88744197
|
A | T | 1 | a0001c0001t0004g0098 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.637+4873T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88744197 | ||||||
chr5:88744204
|
C | CA | 210 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(207): Show | 210 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.637+4865dupT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88744204 | ||||||
chr5:88744329
|
G | A | 1 | a0001c0001t0003g0231 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.637+4741C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88744329 | ||||||
chr5:88744369
|
C | T | 2 | a0001c0001t0002g0243a0001c0001t0002g0244 | 2 | HG03209.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.637+4701G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88744369 | ||||||
chr5:88744463
|
G | C | 5 | a0001c0001t0007g0017a0001c0001t0007g0018a0001c0001t0007g0300others(2): Show | 5 | HG00639.hp1 HG02572.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+4607C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88744463 | ||||||
chr5:88744499
|
C | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.637+4571G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88744499 | ||||||
chr5:88744654
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.637+4416G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88744654 | ||||||
chr5:88744659
|
A | T | 1 | a0001c0001t0001g0131 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.637+4411T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88744659 | ||||||
chr5:88744664
|
A | G | 2 | a0001c0001t0001g0121a0001c0001t0001g0140 | 2 | HG00544.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.637+4406T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88744664 | ||||||
chr5:88744901
|
T | A | 1 | a0001c0001t0036g0015 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.637+4169A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88744901 | ||||||
chr5:88745042
|
T | C | 1 | a0001c0001t0020g0004 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.637+4028A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88745042 | ||||||
chr5:88745064
|
T | A | 1 | a0001c0001t0034g0012 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.637+4006A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88745064 | ||||||
chr5:88745165
|
G | A | 1 | a0001c0001t0003g0240 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.637+3905C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88745165 | ||||||
chr5:88745650
|
G | GA | 209 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(206): Show | 209 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.637+3419dupT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88745650 | ||||||
chr5:88745705
|
C | T | 1 | a0001c0001t0007g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.637+3365G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88745705 | ||||||
chr5:88745964
|
G | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.637+3106C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88745964 | ||||||
chr5:88746037
|
T | A | 24 | a0001c0001t0001g0075a0001c0001t0002g0020a0001c0001t0002g0034others(21): Show | 24 | HG00280.hp1 HG00323.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.637+3033A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88746037 | ||||||
chr5:88746037
|
T | C | 1 | a0001c0001t0007g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.637+3033A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88746037 | ||||||
chr5:88746115
|
C | G | 212 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(209): Show | 212 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.637+2955G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88746115 | ||||||
chr5:88746202
|
G | A | 24 | a0001c0001t0001g0075a0001c0001t0002g0020a0001c0001t0002g0034others(21): Show | 24 | HG00280.hp1 HG00323.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.637+2868C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88746202 | ||||||
chr5:88746216
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.637+2854T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88746216 | ||||||
chr5:88746326
|
T | C | 2 | a0001c0001t0015g0081a0001c0001t0015g0089 | 2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.637+2744A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88746326 | ||||||
chr5:88746441
|
C | CT | 24 | a0001c0001t0001g0075a0001c0001t0002g0020a0001c0001t0002g0034others(21): Show | 24 | HG00280.hp1 HG00323.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.637+2628dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88746441 | ||||||
chr5:88746455
|
TTA | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.637+2613_637+2614d others(4): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88746455 | ||||||
chr5:88746479
|
T | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(105): Show | 108 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.637+2591A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88746479 | ||||||
chr5:88746729
|
G | A | 1 | a0001c0001t0020g0004 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.637+2341C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88746729 | ||||||
chr5:88746952
|
A | G | 4 | a0001c0001t0007g0017a0001c0001t0007g0018a0001c0001t0007g0300others(1): Show | 4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.637+2118T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88746952 | ||||||
chr5:88747210
|
A | C | 1 | a0001c0001t0001g0160 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.637+1860T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88747210 | ||||||
chr5:88747321
|
TTTTTTTT others(5): Show |
T | 1 | a0001c0001t0003g0248 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.637+1737_637+1748d others(14): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88747321 | ||||||
chr5:88747321
|
TTTTTTTT others(321): Show |
T | 97 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(94): Show | 97 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.637+1421_637+1748d others(2): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88747321 | ||||||
chr5:88747322
|
TTTTTTTA others(320): Show |
T | 44 | a0001c0001t0001g0075a0001c0001t0001g0090a0001c0001t0002g0020others(41): Show | 44 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.637+1421_637+1747d others(2): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88747322 | ||||||
chr5:88747333
|
C | CT | 48 | a0001c0001t0001g0273a0001c0001t0002g0048a0001c0001t0002g0188others(45): Show | 48 | HG00099.hp2 HG00642.hp1 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.637+1736dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88747333 | ||||||
chr5:88747333
|
C | CTT | 41 | a0001c0001t0001g0065a0001c0001t0001g0267a0001c0001t0002g0027others(38): Show | 41 | HG01081.hp1 HG01243.hp2 HG01261.hp2 others(38): Show |
intron_variant | MODIFIER | c.637+1735_637+1736d others(4): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88747333 | ||||||
chr5:88747333
|
C | CTTT | 20 | a0001c0001t0002g0007a0001c0001t0002g0021a0001c0001t0002g0070others(17): Show | 20 | HG01433.hp1 HG02027.hp1 HG02293.hp1 others(17): Show |
intron_variant | MODIFIER | c.637+1734_637+1736d others(5): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88747333 | ||||||
chr5:88747333
|
C | CTTTT | 9 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0045others(6): Show | 9 | HG02145.hp2 HG02818.hp2 HG03540.hp2 others(6): Show |
intron_variant | MODIFIER | c.637+1733_637+1736d others(6): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88747333 | ||||||
chr5:88747333
|
C | CTTTTT | 8 | a0001c0001t0002g0198a0001c0001t0002g0200a0001c0001t0002g0202others(5): Show | 8 | HG02129.hp2 NA18951.hp2 NA18969.hp1 others(5): Show |
intron_variant | MODIFIER | c.637+1732_637+1736d others(7): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88747333 | ||||||
chr5:88747333
|
C | CTTTTTT | 9 | a0001c0001t0002g0183a0001c0001t0002g0186a0001c0001t0002g0199others(6): Show | 9 | HG00597.hp1 HG03139.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.637+1731_637+1736d others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88747333 | ||||||
chr5:88747333
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0024g0066 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.637+1727_637+1736d others(12): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88747333 | ||||||
chr5:88747333
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0004g0088 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.637+1725_637+1736d others(14): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88747333 | ||||||
chr5:88747530
|
T | C | 2 | a0001c0001t0019g0067a0001c0001t0024g0066 | 2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.637+1540A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88747530 | ||||||
chr5:88747539
|
C | A | 1 | a0001c0001t0003g0237 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.637+1531G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88747539 | ||||||
chr5:88747591
|
C | T | 1 | a0001c0001t0004g0256 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.637+1479G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88747591 | ||||||
chr5:88747616
|
T | C | 1 | a0001c0001t0017g0253 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.637+1454A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88747616 | ||||||
chr5:88747755
|
C | T | 24 | a0001c0001t0001g0075a0001c0001t0002g0020a0001c0001t0002g0034others(21): Show | 24 | HG00280.hp1 HG00323.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.637+1315G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88747755 | ||||||
chr5:88747839
|
G | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(105): Show | 108 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.637+1231C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88747839 | ||||||
chr5:88748026
|
T | C | 2 | a0001c0001t0014g0290a0001c0001t0014g0295 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.637+1044A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88748026 | ||||||
chr5:88748073
|
T | C | 1 | a0001c0001t0007g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.637+997A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88748073 | ||||||
chr5:88748349
|
C | T | 1 | a0001c0001t0002g0213 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.637+721G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88748349 | ||||||
chr5:88748379
|
T | G | 6 | a0001c0001t0001g0061a0001c0001t0001g0135a0001c0001t0001g0161others(3): Show | 6 | HG01070.hp1 HG01255.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.637+691A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88748379 | ||||||
chr5:88748435
|
G | A | 1 | a0001c0001t0002g0045 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.637+635C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88748435 | ||||||
chr5:88748641
|
C | A | 1 | a0001c0001t0001g0090 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.637+429G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88748641 | ||||||
chr5:88748988
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.637+82A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 6/10 | chr5 | 88748988 | ||||||
chr5:88749212
|
C | A | 15 | a0001c0001t0002g0020a0001c0001t0002g0034a0001c0001t0002g0044others(12): Show | 15 | HG01069.hp1 HG01123.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.590-95G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88749212 | ||||||
chr5:88749428
|
A | T | 2 | a0001c0001t0004g0108a0001c0001t0030g0109 | 2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.590-311T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88749428 | ||||||
chr5:88749758
|
C | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(105): Show | 108 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.590-641G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88749758 | ||||||
chr5:88749786
|
T | G | 1 | a0001c0001t0003g0255 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.590-669A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88749786 | ||||||
chr5:88749842
|
A | C | 1 | a0001c0001t0004g0196 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.590-725T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88749842 | ||||||
chr5:88749844
|
C | G | 1 | a0001c0001t0004g0196 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.590-727G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88749844 | ||||||
chr5:88749872
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.590-755A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88749872 | ||||||
chr5:88750016
|
C | T | 3 | a0001c0001t0002g0183a0001c0001t0008g0184a0001c0001t0015g0089 | 3 | HG00597.hp1 NA18522.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.590-899G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750016 | ||||||
chr5:88750119
|
C | CGAGGCAA others(8): Show |
1 | a0001c0001t0002g0062 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.590-1003_590-1002i others(17): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750119 | ||||||
chr5:88750124
|
A | G | 1 | a0001c0001t0002g0062 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.590-1007T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750124 | ||||||
chr5:88750125
|
G | A | 1 | a0001c0001t0002g0062 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.590-1008C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750125 | ||||||
chr5:88750135
|
G | C | 1 | a0001c0001t0002g0062 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.590-1018C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750135 | ||||||
chr5:88750179
|
T | G | 1 | a0001c0001t0002g0062 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.590-1062A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750179 | ||||||
chr5:88750180
|
G | T | 1 | a0001c0001t0002g0062 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.590-1063C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750180 | ||||||
chr5:88750190
|
A | T | 1 | a0001c0001t0002g0062 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.590-1073T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750190 | ||||||
chr5:88750197
|
T | A | 1 | a0001c0001t0002g0062 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.590-1080A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750197 | ||||||
chr5:88750207
|
A | AT | 25 | a0001c0001t0001g0075a0001c0001t0002g0020a0001c0001t0002g0026others(22): Show | 25 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.590-1091dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750207 | ||||||
chr5:88750207
|
A | T | 1 | a0001c0001t0002g0062 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.590-1090T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750207 | ||||||
chr5:88750208
|
T | A | 1 | a0001c0001t0002g0062 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.590-1091A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750208 | ||||||
chr5:88750209
|
T | A | 1 | a0001c0001t0002g0062 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.590-1092A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750209 | ||||||
chr5:88750234
|
T | C | 1 | a0001c0001t0002g0062 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.590-1117A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750234 | ||||||
chr5:88750247
|
A | G | 5 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(2): Show | 5 | HG02257.hp2 HG02486.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.590-1130T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750247 | ||||||
chr5:88750258
|
T | G | 1 | a0001c0001t0002g0062 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.590-1141A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750258 | ||||||
chr5:88750267
|
T | C | 1 | a0001c0001t0002g0062 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.590-1150A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750267 | ||||||
chr5:88750290
|
A | G | 1 | a0001c0001t0002g0062 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.590-1173T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750290 | ||||||
chr5:88750328
|
C | T | 3 | a0001c0001t0001g0038a0001c0001t0001g0040a0001c0001t0001g0059 | 3 | HG00544.hp1 NA18747.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.590-1211G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750328 | ||||||
chr5:88750337
|
G | A | 2 | a0001c0001t0001g0052a0001c0001t0003g0010 | 2 | HG02040.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.590-1220C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750337 | ||||||
chr5:88750341
|
C | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.590-1224G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750341 | ||||||
chr5:88750374
|
A | T | 1 | a0001c0001t0035g0085 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.590-1257T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750374 | ||||||
chr5:88750543
|
A | G | 3 | a0001c0001t0001g0122a0001c0001t0001g0160a0001c0001t0001g0180 | 3 | NA18963.hp1 NA18971.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.589+1314T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750543 | ||||||
chr5:88750773
|
C | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.589+1084G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750773 | ||||||
chr5:88750824
|
T | C | 1 | a0001c0001t0007g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.589+1033A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88750824 | ||||||
chr5:88751318
|
A | G | 1 | a0001c0001t0007g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.589+539T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88751318 | ||||||
chr5:88751423
|
A | C | 3 | a0001c0001t0005g0013a0001c0001t0005g0014a0001c0001t0036g0015 | 3 | HG01243.hp1 HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.589+434T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88751423 | ||||||
chr5:88751426
|
T | C | 1 | a0001c0001t0004g0011 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.589+431A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88751426 | ||||||
chr5:88751675
|
G | A | 1 | a0001c0001t0004g0208 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.589+182C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 5/10 | chr5 | 88751675 | ||||||
chr5:88752182
|
T | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(105): Show | 108 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.403-139A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88752182 | ||||||
chr5:88752254
|
T | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.403-211A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88752254 | ||||||
chr5:88752394
|
G | C | 1 | a0001c0001t0001g0154 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.403-351C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88752394 | ||||||
chr5:88752640
|
C | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.403-597G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88752640 | ||||||
chr5:88752898
|
C | T | 1 | a0001c0001t0002g0226 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.403-855G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88752898 | ||||||
chr5:88752941
|
G | A | 1 | a0001c0001t0003g0274 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.403-898C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88752941 | ||||||
chr5:88752950
|
A | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.403-907T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88752950 | ||||||
chr5:88753190
|
G | A | 4 | a0001c0001t0007g0017a0001c0001t0007g0018a0001c0001t0007g0300others(1): Show | 4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.403-1147C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88753190 | ||||||
chr5:88753524
|
C | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(207): Show | 210 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.403-1481G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88753524 | ||||||
chr5:88753572
|
G | C | 2 | a0001c0001t0015g0081a0001c0001t0015g0089 | 2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.403-1529C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88753572 | ||||||
chr5:88753721
|
A | C | 1 | a0001c0001t0002g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.403-1678T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88753721 | ||||||
chr5:88753781
|
G | A | 1 | a0001c0001t0007g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.403-1738C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88753781 | ||||||
chr5:88753784
|
G | A | 1 | a0001c0001t0003g0270 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.403-1741C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88753784 | ||||||
chr5:88753912
|
C | T | 1 | a0001c0001t0006g0149 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.403-1869G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88753912 | ||||||
chr5:88754207
|
C | T | 1 | a0001c0001t0007g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.403-2164G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88754207 | ||||||
chr5:88754251
|
T | C | 1 | a0001c0001t0020g0004 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.403-2208A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88754251 | ||||||
chr5:88754284
|
C | T | 1 | a0001c0001t0004g0071 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.403-2241G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88754284 | ||||||
chr5:88754366
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.403-2323A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88754366 | ||||||
chr5:88754570
|
C | A | 3 | a0001c0001t0002g0218a0001c0001t0002g0220a0001c0001t0002g0221 | 3 | NA18949.hp2 NA19070.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.403-2527G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88754570 | ||||||
chr5:88754676
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.403-2633G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88754676 | ||||||
chr5:88754687
|
A | G | 2 | a0001c0001t0003g0233a0001c0001t0003g0235 | 2 | HG02135.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.403-2644T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88754687 | ||||||
chr5:88755107
|
A | G | 2 | a0001c0001t0001g0104a0001c0001t0001g0105 | 2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.403-3064T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88755107 | ||||||
chr5:88755267
|
GTATAGTT others(4): Show |
G | 2 | a0001c0001t0002g0007a0001c0001t0002g0193 | 2 | HG02145.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.403-3235_403-3225d others(13): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88755267 | ||||||
chr5:88755322
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.403-3279A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88755322 | ||||||
chr5:88755502
|
G | C | 1 | a0001c0001t0010g0056 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.403-3459C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88755502 | ||||||
chr5:88755666
|
C | T | 2 | a0001c0001t0002g0044a0001c0001t0002g0174 | 2 | HG01069.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.403-3623G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88755666 | ||||||
chr5:88756028
|
G | A | 1 | a0001c0001t0035g0085 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.403-3985C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88756028 | ||||||
chr5:88756188
|
G | T | 2 | a0001c0001t0002g0127a0001c0001t0002g0128 | 2 | NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.403-4145C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88756188 | ||||||
chr5:88756406
|
G | A | 1 | a0001c0001t0007g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.403-4363C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88756406 | ||||||
chr5:88756639
|
T | C | 1 | a0001c0001t0035g0085 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.402+4546A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88756639 | ||||||
chr5:88756788
|
AT | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(104): Show | 107 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.402+4396delA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88756788 | ||||||
chr5:88756870
|
A | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(105): Show | 108 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.402+4315T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88756870 | ||||||
chr5:88756984
|
G | A | 1 | a0001c0001t0020g0004 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.402+4201C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88756984 | ||||||
chr5:88757013
|
T | G | 1 | a0001c0001t0007g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.402+4172A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88757013 | ||||||
chr5:88757477
|
C | T | 1 | a0001c0001t0003g0249 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.402+3708G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88757477 | ||||||
chr5:88757577
|
C | T | 1 | a0001c0001t0003g0271 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.402+3608G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88757577 | ||||||
chr5:88757682
|
G | A | 1 | a0001c0001t0007g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.402+3503C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88757682 | ||||||
chr5:88757951
|
T | C | 2 | a0001c0001t0005g0083a0001c0001t0005g0084 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.402+3234A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88757951 | ||||||
chr5:88758135
|
C | T | 1 | a0001c0001t0002g0027 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.402+3050G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88758135 | ||||||
chr5:88758475
|
A | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.402+2710T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88758475 | ||||||
chr5:88758748
|
G | A | 6 | a0001c0001t0005g0013a0001c0001t0005g0014a0001c0001t0005g0083others(3): Show | 6 | HG01243.hp1 HG02451.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.402+2437C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88758748 | ||||||
chr5:88758946
|
C | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.402+2239G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88758946 | ||||||
chr5:88759092
|
C | T | 1 | a0001c0001t0007g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.402+2093G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88759092 | ||||||
chr5:88759207
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.402+1978C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88759207 | ||||||
chr5:88759240
|
T | C | 1 | a0001c0001t0002g0268 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.402+1945A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88759240 | ||||||
chr5:88759318
|
A | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.402+1867T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88759318 | ||||||
chr5:88759406
|
C | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.402+1779G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88759406 | ||||||
chr5:88759478
|
G | A | 1 | a0001c0001t0005g0014 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.402+1707C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88759478 | ||||||
chr5:88759496
|
G | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.402+1689C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88759496 | ||||||
chr5:88759652
|
A | G | 2 | a0001c0001t0002g0102a0001c0001t0002g0132 | 2 | NA19065.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.402+1533T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88759652 | ||||||
chr5:88759664
|
T | C | 205 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(202): Show | 205 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.402+1521A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88759664 | ||||||
chr5:88759673
|
T | TAGTC | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.402+1511_402+1512i others(6): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88759673 | ||||||
chr5:88759700
|
T | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.402+1485A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88759700 | ||||||
chr5:88759878
|
G | A | 1 | a0001c0001t0011g0053 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.402+1307C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88759878 | ||||||
chr5:88759944
|
A | G | 134 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(131): Show | 134 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.402+1241T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88759944 | ||||||
chr5:88760158
|
C | A | 212 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(209): Show | 212 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.402+1027G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88760158 | ||||||
chr5:88760186
|
A | G | 1 | a0001c0001t0003g0261 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.402+999T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88760186 | ||||||
chr5:88760630
|
T | G | 1 | a0001c0001t0001g0036 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.402+555A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88760630 | ||||||
chr5:88760631
|
T | G | 1 | a0001c0001t0001g0036 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.402+554A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88760631 | ||||||
chr5:88760731
|
C | T | 1 | a0001c0001t0003g0251 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.402+454G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88760731 | ||||||
chr5:88761123
|
T | C | 1 | a0001c0001t0001g0106 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.402+62A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88761123 | ||||||
chr5:88761169
|
T | C | 2 | a0001c0001t0014g0290a0001c0001t0014g0295 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.402+16A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 4/10 | chr5 | 88761169 | ||||||
chr5:88761357
|
C | T | 1 | a0001c0001t0003g0247 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.259-29G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88761357 | ||||||
chr5:88761520
|
C | T | 1 | a0001c0001t0011g0055 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.259-192G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88761520 | ||||||
chr5:88761614
|
T | C | 1 | a0001c0001t0007g0301 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.259-286A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88761614 | ||||||
chr5:88761973
|
GAGA | G | 6 | a0001c0001t0003g0113a0001c0001t0004g0011a0001c0001t0004g0111others(3): Show | 6 | HG01192.hp1 HG01981.hp2 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.259-648_259-646del others(3): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88761973 | ||||||
chr5:88761979
|
G | T | 3 | a0001c0001t0001g0038a0001c0001t0001g0040a0001c0001t0001g0059 | 3 | HG00544.hp1 NA18747.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.259-651C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88761979 | ||||||
chr5:88762098
|
T | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(105): Show | 108 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.259-770A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88762098 | ||||||
chr5:88762142
|
A | G | 1 | a0001c0001t0001g0024 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.259-814T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88762142 | ||||||
chr5:88762163
|
T | G | 1 | a0001c0001t0020g0004 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.259-835A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88762163 | ||||||
chr5:88762346
|
T | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.259-1018A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88762346 | ||||||
chr5:88762483
|
G | T | 1 | a0001c0001t0001g0052 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.259-1155C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88762483 | ||||||
chr5:88762574
|
A | C | 6 | a0001c0001t0004g0082a0001c0001t0004g0086a0001c0001t0004g0087others(3): Show | 6 | HG01496.hp1 HG01884.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.259-1246T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88762574 | ||||||
chr5:88762583
|
A | AT | 108 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(105): Show | 108 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.259-1256dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88762583 | ||||||
chr5:88762625
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.259-1297G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88762625 | ||||||
chr5:88762656
|
G | C | 1 | a0001c0001t0002g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.259-1328C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88762656 | ||||||
chr5:88762749
|
T | C | 1 | a0001c0001t0012g0151 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.259-1421A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88762749 | ||||||
chr5:88763104
|
T | C | 1 | a0001c0001t0034g0012 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.259-1776A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88763104 | ||||||
chr5:88763143
|
T | C | 1 | a0001c0001t0002g0216 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.259-1815A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88763143 | ||||||
chr5:88763642
|
A | C | 1 | a0001c0001t0034g0012 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.259-2314T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88763642 | ||||||
chr5:88763716
|
G | A | 1 | a0001c0001t0007g0301 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.259-2388C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88763716 | ||||||
chr5:88763834
|
T | C | 1 | a0001c0001t0001g0078 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.259-2506A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88763834 | ||||||
chr5:88764141
|
T | C | 1 | a0001c0001t0004g0286 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.259-2813A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88764141 | ||||||
chr5:88764356
|
G | C | 1 | a0001c0001t0031g0167 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.259-3028C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88764356 | ||||||
chr5:88764487
|
T | C | 4 | a0001c0001t0007g0017a0001c0001t0007g0018a0001c0001t0007g0300others(1): Show | 4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.259-3159A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88764487 | ||||||
chr5:88764494
|
G | T | 205 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(202): Show | 205 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.259-3166C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88764494 | ||||||
chr5:88764504
|
G | A | 212 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(209): Show | 212 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.259-3176C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88764504 | ||||||
chr5:88764576
|
GAGGC | G | 104 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.259-3252_259-3249d others(6): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88764576 | ||||||
chr5:88764676
|
C | T | 3 | a0001c0001t0004g0108a0001c0001t0029g0019a0001c0001t0030g0109 | 3 | HG02572.hp2 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.259-3348G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88764676 | ||||||
chr5:88764807
|
C | CA | 13 | a0001c0001t0002g0048a0001c0001t0002g0218a0001c0001t0002g0220others(10): Show | 13 | HG02257.hp1 HG02572.hp2 HG04115.hp1 others(10): Show |
intron_variant | MODIFIER | c.259-3480dupT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88764807 | ||||||
chr5:88764807
|
CA | C | 15 | a0001c0001t0001g0061a0001c0001t0001g0135a0001c0001t0001g0163others(12): Show | 15 | HG01070.hp1 HG01169.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.259-3480delT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88764807 | ||||||
chr5:88764807
|
CAA | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(95): Show | 98 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.259-3481_259-3480d others(4): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88764807 | ||||||
chr5:88764911
|
T | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(2): Show | 5 | HG02257.hp2 HG02486.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.259-3583A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88764911 | ||||||
chr5:88765199
|
A | G | 1 | a0001c0001t0003g0169 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.259-3871T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88765199 | ||||||
chr5:88765439
|
A | G | 2 | a0001c0001t0002g0044a0001c0001t0002g0174 | 2 | HG01069.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.259-4111T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88765439 | ||||||
chr5:88765716
|
G | A | 2 | a0001c0001t0001g0104a0001c0001t0001g0105 | 2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.259-4388C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88765716 | ||||||
chr5:88765782
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.259-4454A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88765782 | ||||||
chr5:88765798
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.259-4470C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88765798 | ||||||
chr5:88766256
|
G | A | 2 | a0001c0001t0002g0186a0001c0001t0002g0194 | 2 | HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.259-4928C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88766256 | ||||||
chr5:88766482
|
T | C | 5 | a0001c0001t0002g0048a0001c0001t0003g0041a0001c0001t0003g0051others(2): Show | 5 | HG02132.hp1 NA18955.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.259-5154A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88766482 | ||||||
chr5:88767174
|
T | C | 2 | a0001c0001t0015g0081a0001c0001t0015g0089 | 2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.259-5846A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88767174 | ||||||
chr5:88767412
|
G | GAA | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.259-6086_259-6085d others(4): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88767412 | ||||||
chr5:88767631
|
T | C | 1 | a0001c0001t0002g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.259-6303A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88767631 | ||||||
chr5:88767796
|
A | G | 1 | a0001c0001t0004g0088 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.259-6468T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88767796 | ||||||
chr5:88767840
|
C | A | 1 | a0001c0001t0005g0298 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.259-6512G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88767840 | ||||||
chr5:88767955
|
T | C | 1 | a0001c0001t0002g0152 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.259-6627A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88767955 | ||||||
chr5:88768123
|
G | A | 26 | a0001c0001t0001g0075a0001c0001t0001g0090a0001c0001t0002g0020others(23): Show | 26 | HG00280.hp1 HG00323.hp1 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.259-6795C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88768123 | ||||||
chr5:88768138
|
T | C | 1 | a0001c0001t0035g0085 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.259-6810A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88768138 | ||||||
chr5:88768195
|
C | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.259-6867G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88768195 | ||||||
chr5:88768278
|
T | C | 1 | a0001c0001t0003g0185 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.259-6950A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88768278 | ||||||
chr5:88768396
|
T | A | 1 | a0001c0001t0034g0012 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.259-7068A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88768396 | ||||||
chr5:88768460
|
G | A | 1 | a0001c0001t0034g0012 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.259-7132C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88768460 | ||||||
chr5:88768645
|
T | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.259-7317A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88768645 | ||||||
chr5:88768784
|
G | A | 2 | a0001c0001t0001g0104a0001c0001t0001g0105 | 2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.259-7456C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88768784 | ||||||
chr5:88768813
|
A | T | 4 | a0001c0001t0001g0065a0001c0001t0010g0032a0001c0001t0010g0033others(1): Show | 4 | HG01515.hp1 HG01517.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.259-7485T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88768813 | ||||||
chr5:88768827
|
T | A | 1 | a0001c0001t0001g0124 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.259-7499A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88768827 | ||||||
chr5:88768992
|
G | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.259-7664C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88768992 | ||||||
chr5:88769313
|
C | T | 12 | a0001c0001t0003g0169a0001c0001t0003g0233a0001c0001t0003g0235others(9): Show | 12 | HG00099.hp2 HG00642.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.259-7985G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88769313 | ||||||
chr5:88769424
|
C | T | 1 | a0001c0001t0018g0119 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.259-8096G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88769424 | ||||||
chr5:88769446
|
G | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.259-8118C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88769446 | ||||||
chr5:88769703
|
G | A | 2 | a0001c0001t0001g0052a0001c0001t0003g0010 | 2 | HG02040.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.259-8375C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88769703 | ||||||
chr5:88769811
|
A | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.259-8483T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88769811 | ||||||
chr5:88769820
|
G | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.259-8492C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88769820 | ||||||
chr5:88771068
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.259-9740T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88771068 | ||||||
chr5:88771344
|
C | T | 1 | a0001c0001t0035g0085 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.259-10016G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88771344 | ||||||
chr5:88771355
|
C | A | 1 | a0001c0001t0034g0012 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.259-10027G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88771355 | ||||||
chr5:88771628
|
A | G | 2 | a0001c0001t0019g0067a0001c0001t0024g0066 | 2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.259-10300T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88771628 | ||||||
chr5:88771682
|
C | T | 1 | a0001c0001t0001g0125 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.259-10354G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88771682 | ||||||
chr5:88771843
|
C | T | 1 | a0001c0001t0003g0257 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.259-10515G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88771843 | ||||||
chr5:88773608
|
A | G | 3 | a0001c0001t0007g0016a0001c0001t0007g0017a0001c0001t0007g0018 | 3 | HG02896.hp1 HG02897.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.259-12280T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88773608 | ||||||
chr5:88773651
|
T | C | 4 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0019g0067others(1): Show | 4 | HG01891.hp2 HG02572.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.259-12323A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88773651 | ||||||
chr5:88773776
|
G | T | 217 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(214): Show | 217 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.259-12448C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88773776 | ||||||
chr5:88773801
|
T | C | 6 | a0001c0001t0004g0082a0001c0001t0004g0086a0001c0001t0004g0087others(3): Show | 6 | HG01496.hp1 HG01884.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.259-12473A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88773801 | ||||||
chr5:88773986
|
G | A | 2 | a0001c0001t0004g0287a0001c0001t0004g0288 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.259-12658C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88773986 | ||||||
chr5:88774053
|
A | G | 1 | a0001c0001t0001g0173 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.259-12725T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88774053 | ||||||
chr5:88774173
|
T | TTAAC | 5 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(2): Show | 5 | HG02257.hp2 HG02486.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.259-12846_259-1284 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88774173 | ||||||
chr5:88774336
|
C | CT | 106 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(103): Show | 106 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.259-13009dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88774336 | ||||||
chr5:88774448
|
G | A | 1 | a0001c0001t0004g0208 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.259-13120C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88774448 | ||||||
chr5:88774520
|
C | T | 11 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0077others(8): Show | 11 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.259-13192G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88774520 | ||||||
chr5:88774526
|
G | A | 11 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0077others(8): Show | 11 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.259-13198C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88774526 | ||||||
chr5:88774531
|
C | A | 2 | a0001c0001t0002g0007a0001c0001t0002g0193 | 2 | HG02145.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.259-13203G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88774531 | ||||||
chr5:88774574
|
G | A | 1 | a0001c0001t0003g0010 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.259-13246C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88774574 | ||||||
chr5:88774599
|
T | C | 124 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(121): Show | 124 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.259-13271A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88774599 | ||||||
chr5:88774694
|
A | G | 1 | a0001c0001t0003g0240 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.259-13366T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88774694 | ||||||
chr5:88774698
|
G | T | 1 | a0001c0001t0011g0054 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.259-13370C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88774698 | ||||||
chr5:88774991
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.259-13663C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88774991 | ||||||
chr5:88775006
|
G | A | 3 | a0001c0001t0001g0097a0001c0001t0001g0142a0001c0001t0001g0143 | 3 | HG02027.hp2 NA18959.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.259-13678C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88775006 | ||||||
chr5:88775259
|
T | C | 2 | a0001c0001t0002g0007a0001c0001t0002g0193 | 2 | HG02145.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.259-13931A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88775259 | ||||||
chr5:88775334
|
A | G | 1 | a0001c0001t0002g0232 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.259-14006T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88775334 | ||||||
chr5:88775733
|
G | A | 1 | a0001c0001t0006g0149 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.259-14405C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88775733 | ||||||
chr5:88776116
|
G | C | 113 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(110): Show | 113 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.259-14788C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88776116 | ||||||
chr5:88776165
|
T | C | 1 | a0001c0001t0025g0153 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.259-14837A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88776165 | ||||||
chr5:88776198
|
A | G | 1 | a0001c0001t0004g0286 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.259-14870T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88776198 | ||||||
chr5:88776238
|
C | T | 1 | a0001c0001t0003g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.259-14910G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88776238 | ||||||
chr5:88776289
|
G | A | 1 | a0001c0001t0035g0085 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.259-14961C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88776289 | ||||||
chr5:88776533
|
G | A | 4 | a0001c0001t0001g0036a0001c0001t0001g0097a0001c0001t0001g0142others(1): Show | 4 | HG02027.hp2 HG03239.hp1 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.259-15205C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88776533 | ||||||
chr5:88776546
|
C | T | 1 | a0001c0001t0004g0002 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.259-15218G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88776546 | ||||||
chr5:88776849
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.259-15521C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88776849 | ||||||
chr5:88777008
|
T | A | 2 | a0001c0001t0019g0067a0001c0001t0024g0066 | 2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.259-15680A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88777008 | ||||||
chr5:88777024
|
T | G | 11 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0077others(8): Show | 11 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.259-15696A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88777024 | ||||||
chr5:88777411
|
T | A | 17 | a0001c0001t0001g0110a0001c0001t0002g0020a0001c0001t0002g0034others(14): Show | 17 | HG00639.hp2 HG01123.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.259-16083A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88777411 | ||||||
chr5:88777432
|
G | C | 1 | a0001c0001t0001g0181 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.259-16104C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88777432 | ||||||
chr5:88777802
|
G | A | 130 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(127): Show | 130 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.259-16474C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88777802 | ||||||
chr5:88777886
|
A | C | 12 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0077others(9): Show | 12 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.259-16558T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88777886 | ||||||
chr5:88777899
|
C | CT | 181 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0029others(178): Show | 181 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.259-16572dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88777899 | ||||||
chr5:88777899
|
C | CTT | 11 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0142others(8): Show | 11 | HG01081.hp1 HG01981.hp2 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.259-16573_259-1657 others(6): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88777899 | ||||||
chr5:88778155
|
G | A | 1 | a0001c0001t0002g0216 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.259-16827C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88778155 | ||||||
chr5:88778363
|
A | C | 2 | a0001c0001t0002g0224a0001c0001t0002g0225 | 2 | NA18944.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.259-17035T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88778363 | ||||||
chr5:88778588
|
C | T | 1 | a0001c0001t0002g0213 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.259-17260G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88778588 | ||||||
chr5:88778712
|
G | A | 134 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(131): Show | 134 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.259-17384C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88778712 | ||||||
chr5:88778968
|
C | T | 2 | a0001c0001t0001g0008a0001c0001t0002g0003 | 2 | HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.259-17640G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88778968 | ||||||
chr5:88779006
|
G | A | 7 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0045others(4): Show | 7 | HG00280.hp1 HG00323.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.259-17678C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88779006 | ||||||
chr5:88779072
|
T | C | 2 | a0001c0001t0002g0026a0001c0001t0002g0027 | 2 | HG03834.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.259-17744A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88779072 | ||||||
chr5:88779086
|
G | T | 2 | a0001c0001t0003g0091a0001c0001t0007g0016 | 2 | HG03041.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.259-17758C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88779086 | ||||||
chr5:88779088
|
AGTTT | A | 4 | a0001c0001t0001g0022a0001c0001t0001g0063a0001c0001t0001g0064others(1): Show | 4 | NA18979.hp1 NA19057.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.259-17764_259-1776 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88779088 | ||||||
chr5:88779093
|
A | T | 4 | a0001c0001t0001g0022a0001c0001t0001g0063a0001c0001t0001g0064others(1): Show | 4 | NA18979.hp1 NA19057.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.259-17765T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88779093 | ||||||
chr5:88779137
|
T | G | 2 | a0001c0001t0007g0017a0001c0001t0007g0018 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.259-17809A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88779137 | ||||||
chr5:88779195
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.259-17867T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88779195 | ||||||
chr5:88779332
|
T | C | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(1): Show | 4 | HG02257.hp2 HG02486.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.259-18004A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88779332 | ||||||
chr5:88779466
|
G | T | 1 | a0001c0001t0001g0154 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.259-18138C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88779466 | ||||||
chr5:88779488
|
A | G | 1 | a0001c0001t0004g0286 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.259-18160T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88779488 | ||||||
chr5:88779496
|
C | G | 1 | a0001c0001t0002g0042 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.259-18168G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88779496 | ||||||
chr5:88779601
|
T | TTG | 158 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0029others(155): Show | 158 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.259-18275_259-1827 others(6): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88779601 | ||||||
chr5:88779601
|
T | TTGTG | 7 | a0001c0001t0001g0001a0001c0001t0002g0030a0001c0001t0002g0062others(4): Show | 7 | HG01358.hp1 NA18955.hp1 NA18980.hp2 others(4): Show |
intron_variant | MODIFIER | c.259-18277_259-1827 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88779601 | ||||||
chr5:88779760
|
G | GT | 113 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(110): Show | 113 | HG00544.hp1 HG00597.hp1 HG00741.hp1 others(110): Show |
intron_variant | MODIFIER | c.259-18433dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88779760 | ||||||
chr5:88779760
|
G | GTT | 121 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(118): Show | 121 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.259-18434_259-1843 others(6): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88779760 | ||||||
chr5:88779760
|
G | GTTT | 10 | a0001c0001t0001g0105a0001c0001t0002g0045a0001c0001t0002g0232others(7): Show | 10 | HG00280.hp1 HG00323.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.259-18435_259-1843 others(7): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88779760 | ||||||
chr5:88779864
|
A | G | 2 | a0001c0001t0003g0259a0001c0001t0003g0282 | 2 | NA18941.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.259-18536T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88779864 | ||||||
chr5:88779955
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.259-18627C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88779955 | ||||||
chr5:88779993
|
A | C | 1 | a0001c0001t0001g0141 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.259-18665T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88779993 | ||||||
chr5:88780533
|
T | C | 1 | a0001c0001t0001g0180 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.259-19205A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88780533 | ||||||
chr5:88780617
|
C | T | 1 | a0001c0001t0002g0028 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.259-19289G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88780617 | ||||||
chr5:88780634
|
ATACT | A | 9 | a0001c0001t0004g0082a0001c0001t0004g0086a0001c0001t0004g0087others(6): Show | 9 | HG01496.hp1 HG01884.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.259-19310_259-1930 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88780634 | ||||||
chr5:88780710
|
T | C | 1 | a0001c0001t0034g0012 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.259-19382A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88780710 | ||||||
chr5:88780728
|
A | G | 2 | a0001c0001t0007g0017a0001c0001t0007g0018 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.259-19400T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88780728 | ||||||
chr5:88780792
|
T | G | 3 | a0001c0001t0004g0108a0001c0001t0030g0109a0001c0001t0034g0012 | 3 | HG00639.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.259-19464A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88780792 | ||||||
chr5:88780866
|
G | C | 3 | a0001c0001t0001g0072a0001c0001t0001g0077a0001c0001t0001g0078 | 3 | HG01261.hp1 HG02809.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.259-19538C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88780866 | ||||||
chr5:88781182
|
T | C | 1 | a0001c0001t0002g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.259-19854A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88781182 | ||||||
chr5:88781306
|
A | G | 1 | a0001c0001t0003g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.259-19978T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88781306 | ||||||
chr5:88781364
|
T | C | 1 | a0001c0001t0003g0169 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.259-20036A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88781364 | ||||||
chr5:88781374
|
T | C | 1 | a0001c0001t0001g0031 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.259-20046A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88781374 | ||||||
chr5:88781424
|
C | G | 1 | a0001c0001t0001g0058 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.259-20096G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88781424 | ||||||
chr5:88781432
|
C | T | 4 | a0001c0001t0002g0020a0001c0001t0011g0053a0001c0001t0011g0054others(1): Show | 4 | HG02109.hp2 NA18982.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.259-20104G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88781432 | ||||||
chr5:88781520
|
AC | A | 3 | a0001c0001t0001g0072a0001c0001t0001g0077a0001c0001t0001g0078 | 3 | HG01261.hp1 HG02809.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.259-20193delG | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88781520 | ||||||
chr5:88781594
|
T | C | 2 | a0001c0001t0002g0007a0001c0001t0002g0193 | 2 | HG02145.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.259-20266A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88781594 | ||||||
chr5:88781631
|
G | A | 134 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(131): Show | 134 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.259-20303C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88781631 | ||||||
chr5:88781711
|
CCTGTAAT others(7): Show |
C | 1 | a0001c0001t0034g0012 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.259-20397_259-2038 others(18): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88781711 | ||||||
chr5:88781737
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.259-20409G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88781737 | ||||||
chr5:88781801
|
C | T | 1 | a0001c0001t0003g0091 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.259-20473G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88781801 | ||||||
chr5:88782464
|
CA | C | 223 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(220): Show | 223 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.259-21137delT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88782464 | ||||||
chr5:88782472
|
A | T | 3 | a0001c0001t0002g0073a0001c0001t0016g0074a0001c0001t0016g0079 | 3 | HG01169.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.259-21144T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88782472 | ||||||
chr5:88782508
|
G | A | 141 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(138): Show | 141 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.259-21180C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88782508 | ||||||
chr5:88782941
|
T | C | 1 | a0001c0001t0002g0049 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.259-21613A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88782941 | ||||||
chr5:88783067
|
T | C | 4 | a0001c0001t0001g0075a0001c0001t0004g0009a0001c0001t0004g0071others(1): Show | 4 | HG00733.hp1 HG01081.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+21531A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88783067 | ||||||
chr5:88783123
|
C | G | 1 | a0001c0001t0001g0159 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.258+21475G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88783123 | ||||||
chr5:88783193
|
G | T | 223 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(220): Show | 223 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.258+21405C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88783193 | ||||||
chr5:88783269
|
T | G | 4 | a0001c0001t0003g0091a0001c0001t0007g0016a0001c0001t0007g0017others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+21329A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88783269 | ||||||
chr5:88783322
|
C | T | 4 | a0001c0001t0001g0075a0001c0001t0004g0009a0001c0001t0004g0071others(1): Show | 4 | HG00733.hp1 HG01081.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+21276G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88783322 | ||||||
chr5:88783366
|
C | T | 2 | a0001c0001t0019g0067a0001c0001t0024g0066 | 2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.258+21232G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88783366 | ||||||
chr5:88783394
|
C | T | 1 | a0001c0001t0023g0209 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.258+21204G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88783394 | ||||||
chr5:88783553
|
C | G | 1 | a0001c0001t0008g0184 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.258+21045G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88783553 | ||||||
chr5:88783554
|
C | T | 10 | a0001c0001t0001g0061a0001c0001t0001g0123a0001c0001t0001g0135others(7): Show | 10 | HG00280.hp2 HG01070.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.258+21044G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88783554 | ||||||
chr5:88783682
|
C | T | 130 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(127): Show | 130 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.258+20916G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88783682 | ||||||
chr5:88783888
|
A | G | 3 | a0001c0001t0002g0048a0001c0001t0003g0041a0001c0001t0003g0051 | 3 | NA18955.hp1 NA18966.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.258+20710T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88783888 | ||||||
chr5:88784019
|
A | G | 1 | a0001c0001t0002g0034 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.258+20579T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88784019 | ||||||
chr5:88784235
|
A | G | 2 | a0001c0001t0001g0104a0001c0001t0001g0105 | 2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.258+20363T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88784235 | ||||||
chr5:88784925
|
T | C | 1 | a0001c0001t0032g0130 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.258+19673A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88784925 | ||||||
chr5:88785279
|
T | TAC | 19 | a0001c0001t0001g0008a0001c0001t0002g0003a0001c0001t0002g0028others(16): Show | 19 | HG00673.hp1 HG01169.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.258+19317_258+1931 others(6): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88785279 | ||||||
chr5:88785279
|
T | TACAC | 8 | a0001c0001t0001g0059a0001c0001t0002g0182a0001c0001t0005g0013others(5): Show | 8 | HG01099.hp1 HG01243.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.258+19315_258+1931 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88785279 | ||||||
chr5:88785279
|
T | TACACAC | 6 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0002g0186others(3): Show | 6 | HG01255.hp2 HG02280.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.258+19313_258+1931 others(10): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88785279 | ||||||
chr5:88785279
|
T | TACACACA others(1): Show |
3 | a0001c0001t0001g0052a0001c0001t0002g0174a0001c0001t0003g0076 | 3 | HG01069.hp1 HG02040.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.258+19311_258+1931 others(12): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88785279 | ||||||
chr5:88785279
|
T | TACACACA others(3): Show |
1 | a0001c0001t0002g0044 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.258+19309_258+1931 others(14): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88785279 | ||||||
chr5:88785279
|
TAC | T | 51 | a0001c0001t0001g0029a0001c0001t0001g0267a0001c0001t0001g0273others(48): Show | 51 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.258+19317_258+1931 others(6): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88785279 | ||||||
chr5:88785279
|
TACAC | T | 30 | a0001c0001t0001g0110a0001c0001t0002g0020a0001c0001t0002g0034others(27): Show | 30 | HG00639.hp2 HG01192.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.258+19315_258+1931 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88785279 | ||||||
chr5:88785279
|
TACACAC | T | 7 | a0001c0001t0001g0090a0001c0001t0001g0123a0001c0001t0001g0131others(4): Show | 7 | HG00280.hp1 HG00323.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.258+19313_258+1931 others(10): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88785279 | ||||||
chr5:88785279
|
TACACACA others(1): Show |
T | 86 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(83): Show | 86 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.258+19311_258+1931 others(12): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88785279 | ||||||
chr5:88785279
|
TACACACA others(3): Show |
T | 9 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(6): Show | 9 | HG00099.hp1 HG00741.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.258+19309_258+1931 others(14): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88785279 | ||||||
chr5:88785279
|
TACACACA others(9): Show |
T | 2 | a0001c0001t0001g0036a0001c0001t0001g0058 | 2 | HG01978.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.258+19303_258+1931 others(20): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88785279 | ||||||
chr5:88785617
|
G | A | 1 | a0001c0001t0003g0269 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.258+18981C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88785617 | ||||||
chr5:88785679
|
G | A | 17 | a0001c0001t0001g0110a0001c0001t0002g0020a0001c0001t0002g0034others(14): Show | 17 | HG00639.hp2 HG01123.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.258+18919C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88785679 | ||||||
chr5:88785762
|
AAGTT | A | 130 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(127): Show | 130 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.258+18832_258+1883 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88785762 | ||||||
chr5:88785790
|
G | T | 1 | a0001c0001t0007g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.258+18808C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88785790 | ||||||
chr5:88785845
|
A | T | 1 | a0001c0001t0001g0155 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.258+18753T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88785845 | ||||||
chr5:88786084
|
G | A | 2 | a0001c0001t0002g0021a0001c0001t0003g0238 | 2 | HG01934.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.258+18514C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88786084 | ||||||
chr5:88786121
|
G | A | 1 | a0001c0001t0003g0248 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.258+18477C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88786121 | ||||||
chr5:88786463
|
G | GA | 20 | a0001c0001t0002g0073a0001c0001t0003g0185a0001c0001t0003g0255others(17): Show | 20 | HG00741.hp1 HG01169.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.258+18134dupT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88786463 | ||||||
chr5:88786488
|
TAAAC | T | 14 | a0001c0001t0002g0183a0001c0001t0002g0198a0001c0001t0002g0199others(11): Show | 14 | HG00597.hp1 HG04184.hp1 NA18951.hp2 others(11): Show |
intron_variant | MODIFIER | c.258+18106_258+1810 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88786488 | ||||||
chr5:88786673
|
GCTACATA others(6): Show |
G | 2 | a0001c0001t0019g0067a0001c0001t0024g0066 | 2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.258+17912_258+1792 others(17): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88786673 | ||||||
chr5:88786729
|
T | G | 1 | a0001c0001t0004g0002 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.258+17869A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88786729 | ||||||
chr5:88786732
|
A | G | 2 | a0001c0001t0003g0252a0001c0001t0004g0246 | 2 | HG00642.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.258+17866T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88786732 | ||||||
chr5:88786862
|
T | G | 1 | a0001c0001t0032g0130 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.258+17736A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88786862 | ||||||
chr5:88786887
|
T | G | 1 | a0001c0001t0011g0054 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.258+17711A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88786887 | ||||||
chr5:88786922
|
A | G | 1 | a0001c0001t0002g0206 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.258+17676T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88786922 | ||||||
chr5:88786925
|
T | A | 1 | a0001c0001t0001g0063 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.258+17673A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88786925 | ||||||
chr5:88787077
|
G | A | 4 | a0001c0001t0004g0283a0001c0001t0004g0284a0001c0001t0004g0287others(1): Show | 4 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+17521C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88787077 | ||||||
chr5:88787116
|
TTAA | T | 73 | a0001c0001t0001g0031a0001c0001t0001g0036a0001c0001t0001g0038others(70): Show | 73 | HG00544.hp1 HG00597.hp1 HG01069.hp1 others(70): Show |
intron_variant | MODIFIER | c.258+17479_258+1748 others(7): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88787116 | ||||||
chr5:88787230
|
A | C | 2 | a0001c0001t0001g0101a0001c0001t0004g0099 | 2 | HG02818.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.258+17368T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88787230 | ||||||
chr5:88787371
|
A | C | 1 | a0001c0001t0001g0141 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.258+17227T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88787371 | ||||||
chr5:88787418
|
TA | T | 7 | a0001c0001t0001g0110a0001c0001t0003g0113a0001c0001t0004g0011others(4): Show | 7 | HG00639.hp2 HG01192.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.258+17179delT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88787418 | ||||||
chr5:88787429
|
G | C | 1 | a0001c0001t0031g0167 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.258+17169C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88787429 | ||||||
chr5:88787458
|
T | C | 5 | a0001c0001t0003g0233a0001c0001t0003g0235a0001c0001t0003g0252others(2): Show | 5 | HG00642.hp1 HG01192.hp2 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.258+17140A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88787458 | ||||||
chr5:88787470
|
A | T | 9 | a0001c0001t0004g0082a0001c0001t0004g0086a0001c0001t0004g0087others(6): Show | 9 | HG01496.hp1 HG01884.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.258+17128T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88787470 | ||||||
chr5:88787485
|
C | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG02257.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.258+17113G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88787485 | ||||||
chr5:88787636
|
T | C | 7 | a0001c0001t0001g0110a0001c0001t0003g0113a0001c0001t0004g0011others(4): Show | 7 | HG00639.hp2 HG01192.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.258+16962A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88787636 | ||||||
chr5:88787741
|
A | C | 2 | a0001c0001t0003g0261a0001c0001t0003g0292 | 2 | HG01069.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.258+16857T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88787741 | ||||||
chr5:88787794
|
A | T | 4 | a0001c0001t0003g0091a0001c0001t0007g0016a0001c0001t0007g0017others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+16804T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88787794 | ||||||
chr5:88788158
|
T | C | 7 | a0001c0001t0001g0065a0001c0001t0002g0021a0001c0001t0002g0030others(4): Show | 7 | HG02027.hp1 NA18747.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.258+16440A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88788158 | ||||||
chr5:88788165
|
AGTTT | A | 5 | a0001c0001t0002g0206a0001c0001t0003g0091a0001c0001t0007g0016others(2): Show | 5 | HG02523.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.258+16429_258+1643 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88788165 | ||||||
chr5:88788174
|
GTTTGTTT others(1): Show |
G | 71 | a0001c0001t0001g0031a0001c0001t0001g0036a0001c0001t0001g0038others(68): Show | 71 | HG00544.hp1 HG00597.hp1 HG01069.hp1 others(68): Show |
intron_variant | MODIFIER | c.258+16416_258+1642 others(12): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88788174 | ||||||
chr5:88788174
|
GTTTGTTT others(9): Show |
G | 1 | a0001c0001t0002g0199 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.258+16408_258+1642 others(20): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88788174 | ||||||
chr5:88788178
|
G | A | 1 | a0001c0001t0034g0012 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.258+16420C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88788178 | ||||||
chr5:88788178
|
G | GTTTA | 16 | a0001c0001t0002g0045a0001c0001t0002g0232a0001c0001t0003g0230others(13): Show | 16 | HG00280.hp1 HG00323.hp1 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.258+16416_258+1641 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88788178 | ||||||
chr5:88788178
|
G | GTTTATTT others(1): Show |
26 | a0001c0001t0001g0075a0001c0001t0001g0110a0001c0001t0002g0020others(23): Show | 26 | HG00639.hp2 HG00733.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.258+16412_258+1641 others(12): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88788178 | ||||||
chr5:88788178
|
G | GTTTATTT others(5): Show |
3 | a0001c0001t0002g0034a0001c0001t0002g0049a0001c0001t0004g0009 | 3 | HG01981.hp1 HG03688.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.258+16408_258+1641 others(16): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88788178 | ||||||
chr5:88788178
|
G | GTTTATTT others(9): Show |
2 | a0001c0001t0002g0050a0001c0001t0020g0004 | 2 | HG01496.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.258+16404_258+1641 others(20): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88788178 | ||||||
chr5:88788178
|
G | GTTTGTTT others(1): Show |
30 | a0001c0001t0001g0072a0001c0001t0001g0090a0001c0001t0001g0093others(27): Show | 30 | HG00597.hp2 HG00673.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.258+16419_258+1642 others(12): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88788178 | ||||||
chr5:88788178
|
G | GTTTGTTT others(5): Show |
1 | a0001c0001t0001g0077 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.258+16419_258+1642 others(16): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88788178 | ||||||
chr5:88788178
|
GTTTA | G | 21 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(18): Show | 21 | HG00741.hp1 HG01243.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.258+16416_258+1641 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88788178 | ||||||
chr5:88788182
|
A | G | 1 | a0001c0001t0001g0078 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.258+16416T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88788182 | ||||||
chr5:88788199
|
T | A | 28 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(25): Show | 28 | HG00597.hp2 HG00673.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.258+16399A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88788199 | ||||||
chr5:88788199
|
T | TTTATTTA others(1): Show |
55 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0039others(52): Show | 55 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.258+16398_258+1639 others(12): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88788199 | ||||||
chr5:88788286
|
C | T | 14 | a0001c0001t0002g0183a0001c0001t0002g0198a0001c0001t0002g0199others(11): Show | 14 | HG00597.hp1 HG04184.hp1 NA18951.hp2 others(11): Show |
intron_variant | MODIFIER | c.258+16312G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88788286 | ||||||
chr5:88788305
|
A | G | 1 | a0001c0001t0004g0002 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.258+16293T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88788305 | ||||||
chr5:88788713
|
G | A | 1 | a0001c0001t0010g0056 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.258+15885C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88788713 | ||||||
chr5:88789151
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.258+15447T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88789151 | ||||||
chr5:88789171
|
CT | C | 7 | a0001c0001t0001g0110a0001c0001t0003g0113a0001c0001t0004g0011others(4): Show | 7 | HG00639.hp2 HG01192.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.258+15426delA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88789171 | ||||||
chr5:88789297
|
G | T | 1 | a0001c0001t0035g0085 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.258+15301C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88789297 | ||||||
chr5:88789409
|
C | G | 2 | a0001c0001t0006g0148a0001c0001t0006g0149 | 2 | NA18945.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.258+15189G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88789409 | ||||||
chr5:88789604
|
A | G | 3 | a0001c0001t0001g0135a0001c0001t0001g0166a0001c0001t0001g0168 | 3 | HG00280.hp2 HG01070.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.258+14994T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88789604 | ||||||
chr5:88789660
|
A | T | 1 | a0001c0001t0004g0108 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.258+14938T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88789660 | ||||||
chr5:88789922
|
A | G | 1 | a0001c0001t0001g0267 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.258+14676T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88789922 | ||||||
chr5:88790008
|
C | T | 2 | a0001c0001t0003g0281a0001c0001t0003g0293 | 2 | HG02132.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.258+14590G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88790008 | ||||||
chr5:88790028
|
T | C | 2 | a0001c0001t0002g0243a0001c0001t0002g0244 | 2 | HG03209.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.258+14570A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88790028 | ||||||
chr5:88790185
|
CTTCCT | C | 3 | a0001c0001t0008g0035a0001c0001t0008g0068a0001c0001t0008g0069 | 3 | HG01433.hp1 HG01975.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.258+14408_258+1441 others(9): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88790185 | ||||||
chr5:88790250
|
A | G | 1 | a0001c0001t0004g0002 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.258+14348T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88790250 | ||||||
chr5:88790283
|
A | G | 4 | a0001c0001t0006g0133a0001c0001t0006g0134a0001c0001t0006g0148others(1): Show | 4 | NA18945.hp1 NA18970.hp1 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+14315T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88790283 | ||||||
chr5:88790288
|
C | T | 1 | a0001c0001t0002g0206 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.258+14310G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88790288 | ||||||
chr5:88790295
|
T | C | 131 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(128): Show | 131 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.258+14303A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88790295 | ||||||
chr5:88790307
|
A | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(132): Show | 135 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.258+14291T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88790307 | ||||||
chr5:88790454
|
T | C | 1 | a0001c0001t0002g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.258+14144A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88790454 | ||||||
chr5:88790467
|
A | C | 2 | a0001c0001t0002g0026a0001c0001t0002g0027 | 2 | HG03834.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.258+14131T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88790467 | ||||||
chr5:88790729
|
T | C | 1 | a0001c0001t0003g0091 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.258+13869A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88790729 | ||||||
chr5:88790863
|
G | A | 1 | a0001c0001t0023g0209 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.258+13735C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88790863 | ||||||
chr5:88790904
|
C | G | 1 | a0001c0001t0003g0242 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.258+13694G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88790904 | ||||||
chr5:88791579
|
T | C | 4 | a0001c0001t0003g0091a0001c0001t0007g0016a0001c0001t0007g0017others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+13019A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88791579 | ||||||
chr5:88791610
|
A | G | 1 | a0001c0001t0029g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.258+12988T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88791610 | ||||||
chr5:88791856
|
T | C | 9 | a0001c0001t0004g0082a0001c0001t0004g0086a0001c0001t0004g0087others(6): Show | 9 | HG01496.hp1 HG01884.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.258+12742A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88791856 | ||||||
chr5:88791947
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.258+12651T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88791947 | ||||||
chr5:88792387
|
G | A | 82 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(79): Show | 82 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.258+12211C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88792387 | ||||||
chr5:88792407
|
T | C | 1 | a0001c0001t0003g0010 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.258+12191A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88792407 | ||||||
chr5:88792421
|
A | G | 1 | a0001c0001t0003g0185 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.258+12177T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88792421 | ||||||
chr5:88792476
|
C | T | 1 | a0001c0001t0002g0102 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.258+12122G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88792476 | ||||||
chr5:88792622
|
G | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(132): Show | 135 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.258+11976C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88792622 | ||||||
chr5:88792758
|
G | A | 1 | a0001c0001t0003g0255 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.258+11840C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88792758 | ||||||
chr5:88793015
|
T | C | 1 | a0001c0001t0001g0001 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.258+11583A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88793015 | ||||||
chr5:88793244
|
G | A | 1 | a0001c0001t0004g0196 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.258+11354C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88793244 | ||||||
chr5:88793327
|
TG | T | 74 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0036others(71): Show | 74 | HG00544.hp1 HG00597.hp1 HG01099.hp1 others(71): Show |
intron_variant | MODIFIER | c.258+11270delC | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88793327 | ||||||
chr5:88793438
|
T | C | 2 | a0001c0001t0004g0286a0001c0001t0004g0291 | 2 | HG02559.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.258+11160A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88793438 | ||||||
chr5:88793696
|
C | A | 1 | a0001c0001t0021g0197 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.258+10902G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88793696 | ||||||
chr5:88793740
|
G | A | 1 | a0001c0001t0002g0062 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.258+10858C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88793740 | ||||||
chr5:88794459
|
G | A | 1 | a0001c0001t0010g0056 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.258+10139C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88794459 | ||||||
chr5:88794647
|
T | C | 1 | a0001c0001t0002g0021 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.258+9951A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88794647 | ||||||
chr5:88795143
|
T | C | 3 | a0001c0001t0002g0127a0001c0001t0002g0128a0001c0001t0025g0153 | 3 | HG02622.hp1 NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.258+9455A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88795143 | ||||||
chr5:88795271
|
C | G | 1 | a0001c0001t0001g0135 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.258+9327G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88795271 | ||||||
chr5:88795615
|
A | G | 9 | a0001c0001t0004g0082a0001c0001t0004g0086a0001c0001t0004g0087others(6): Show | 9 | HG01496.hp1 HG01884.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.258+8983T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88795615 | ||||||
chr5:88795676
|
T | C | 1 | a0001c0001t0001g0147 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.258+8922A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88795676 | ||||||
chr5:88796051
|
T | G | 17 | a0001c0001t0001g0110a0001c0001t0002g0020a0001c0001t0002g0034others(14): Show | 17 | HG00639.hp2 HG01123.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.258+8547A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88796051 | ||||||
chr5:88796133
|
A | T | 266 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(263): Show | 266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.258+8465T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88796133 | ||||||
chr5:88796197
|
T | C | 2 | a0001c0001t0005g0083a0001c0001t0005g0084 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.258+8401A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88796197 | ||||||
chr5:88796376
|
T | G | 1 | a0001c0001t0004g0103 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.258+8222A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88796376 | ||||||
chr5:88796521
|
C | T | 10 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0077others(7): Show | 10 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.258+8077G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88796521 | ||||||
chr5:88796562
|
T | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(132): Show | 135 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.258+8036A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88796562 | ||||||
chr5:88796590
|
A | G | 5 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(2): Show | 5 | HG02257.hp2 HG02486.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.258+8008T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88796590 | ||||||
chr5:88796749
|
T | C | 4 | a0001c0001t0002g0189a0001c0001t0002g0212a0001c0001t0002g0214others(1): Show | 4 | NA18945.hp2 NA18982.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+7849A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88796749 | ||||||
chr5:88796764
|
A | G | 2 | a0001c0001t0004g0285a0001c0001t0004g0289 | 2 | HG01496.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.258+7834T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88796764 | ||||||
chr5:88796908
|
T | C | 1 | a0001c0001t0034g0012 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.258+7690A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88796908 | ||||||
chr5:88796910
|
G | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(132): Show | 135 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.258+7688C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88796910 | ||||||
chr5:88797017
|
A | G | 2 | a0001c0001t0002g0102a0001c0001t0002g0132 | 2 | NA19065.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.258+7581T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88797017 | ||||||
chr5:88797241
|
T | C | 4 | a0001c0001t0005g0013a0001c0001t0005g0014a0001c0001t0005g0298others(1): Show | 4 | HG01243.hp1 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+7357A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88797241 | ||||||
chr5:88797322
|
C | T | 10 | a0001c0001t0004g0082a0001c0001t0004g0086a0001c0001t0004g0087others(7): Show | 10 | HG01496.hp1 HG01884.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.258+7276G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88797322 | ||||||
chr5:88797336
|
T | C | 2 | a0001c0001t0001g0121a0001c0001t0001g0140 | 2 | HG00544.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.258+7262A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88797336 | ||||||
chr5:88797343
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.258+7255G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88797343 | ||||||
chr5:88797448
|
C | T | 2 | a0001c0001t0015g0081a0001c0001t0015g0089 | 2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.258+7150G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88797448 | ||||||
chr5:88797449
|
C | G | 1 | a0001c0001t0004g0112 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.258+7149G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88797449 | ||||||
chr5:88797453
|
GC | G | 39 | a0001c0001t0001g0024a0001c0001t0001g0072a0001c0001t0001g0075others(36): Show | 39 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.258+7144delG | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88797453 | ||||||
chr5:88797454
|
C | CT | 21 | a0001c0001t0001g0001a0001c0001t0001g0039a0001c0001t0001g0061others(18): Show | 21 | HG00597.hp2 HG01070.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.258+7143_258+7144i others(3): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88797454 | ||||||
chr5:88797454
|
C | CTT | 5 | a0001c0001t0001g0126a0001c0001t0001g0228a0001c0001t0002g0243others(2): Show | 5 | HG02109.hp1 HG03209.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.258+7143_258+7144i others(4): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88797454 | ||||||
chr5:88797454
|
CCTTTTTT others(9): Show |
C | 1 | a0001c0001t0009g0175 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.258+7128_258+7143d others(18): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88797454 | ||||||
chr5:88797455
|
C | CT | 68 | a0001c0001t0001g0031a0001c0001t0001g0036a0001c0001t0001g0038others(65): Show | 68 | HG00544.hp1 HG00597.hp1 HG01099.hp1 others(65): Show |
intron_variant | MODIFIER | c.258+7142dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88797455 | ||||||
chr5:88797455
|
C | CTT | 14 | a0001c0001t0001g0029a0001c0001t0001g0059a0001c0001t0001g0065others(11): Show | 14 | HG01515.hp1 HG01517.hp1 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.258+7141_258+7142d others(4): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88797455 | ||||||
chr5:88797455
|
C | T | 95 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0039others(92): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.258+7143G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88797455 | ||||||
chr5:88797455
|
CT | C | 33 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0002g0234others(30): Show | 33 | HG00099.hp2 HG00673.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.258+7142delA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88797455 | ||||||
chr5:88797455
|
CTT | C | 6 | a0001c0001t0005g0013a0001c0001t0005g0014a0001c0001t0005g0298others(3): Show | 6 | HG01243.hp1 HG01891.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.258+7141_258+7142d others(4): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88797455 | ||||||
chr5:88797456
|
T | G | 1 | a0001c0001t0002g0049 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.258+7142A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88797456 | ||||||
chr5:88797457
|
T | C | 1 | a0001c0001t0002g0049 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.258+7141A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88797457 | ||||||
chr5:88797537
|
T | C | 2 | a0001c0001t0010g0032a0001c0001t0010g0033 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.258+7061A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88797537 | ||||||
chr5:88798176
|
A | G | 1 | a0001c0001t0011g0055 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.258+6422T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88798176 | ||||||
chr5:88798418
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.258+6180C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88798418 | ||||||
chr5:88798431
|
G | A | 4 | a0001c0001t0003g0091a0001c0001t0007g0016a0001c0001t0007g0017others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+6167C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88798431 | ||||||
chr5:88798452
|
C | T | 1 | a0001c0001t0003g0169 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.258+6146G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88798452 | ||||||
chr5:88798564
|
T | C | 2 | a0001c0001t0002g0183a0001c0001t0008g0184 | 2 | HG00597.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.258+6034A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88798564 | ||||||
chr5:88798580
|
A | G | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | NA18960.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.258+6018T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88798580 | ||||||
chr5:88798675
|
T | C | 11 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0077others(8): Show | 11 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.258+5923A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88798675 | ||||||
chr5:88798790
|
G | T | 1 | a0001c0001t0013g0156 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.258+5808C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88798790 | ||||||
chr5:88798795
|
T | C | 1 | a0001c0001t0003g0231 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.258+5803A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88798795 | ||||||
chr5:88798806
|
G | A | 7 | a0001c0001t0001g0110a0001c0001t0003g0113a0001c0001t0004g0011others(4): Show | 7 | HG00639.hp2 HG01192.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.258+5792C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88798806 | ||||||
chr5:88798814
|
G | A | 2 | a0001c0001t0007g0300a0001c0001t0007g0301 | 2 | HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.258+5784C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88798814 | ||||||
chr5:88798859
|
T | C | 1 | a0001c0001t0001g0005 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.258+5739A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88798859 | ||||||
chr5:88799373
|
G | T | 1 | a0001c0001t0003g0185 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.258+5225C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799373 | ||||||
chr5:88799809
|
T | C | 1 | a0001c0001t0020g0004 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.258+4789A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799809 | ||||||
chr5:88799839
|
G | T | 4 | a0001c0001t0003g0091a0001c0001t0007g0016a0001c0001t0007g0017others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+4759C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799839 | ||||||
chr5:88799849
|
TTC | T | 29 | a0001c0001t0001g0267a0001c0001t0001g0273a0001c0001t0002g0268others(26): Show | 29 | HG01069.hp2 HG01070.hp2 HG01358.hp2 others(26): Show |
intron_variant | MODIFIER | c.258+4747_258+4748d others(4): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799849 | ||||||
chr5:88799870
|
T | A | 1 | a0001c0001t0003g0281 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.258+4728A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799870 | ||||||
chr5:88799870
|
T | TCA | 3 | a0001c0001t0003g0238a0001c0001t0003g0255a0001c0001t0004g0256 | 3 | HG00741.hp1 HG01934.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.258+4726_258+4727d others(4): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799870 | ||||||
chr5:88799870
|
T | TCATA | 6 | a0001c0001t0002g0026a0001c0001t0002g0243a0001c0001t0004g0108others(3): Show | 6 | HG00280.hp1 HG02055.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.258+4727_258+4728i others(6): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799870 | ||||||
chr5:88799870
|
T | TCATACA | 5 | a0001c0001t0002g0027a0001c0001t0002g0045a0001c0001t0003g0076others(2): Show | 5 | HG01243.hp1 HG02647.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.258+4727_258+4728i others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799870 | ||||||
chr5:88799870
|
T | TCATACAC others(3): Show |
1 | a0001c0001t0005g0014 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.258+4727_258+4728i others(12): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799870 | ||||||
chr5:88799870
|
T | TCATACAC others(5): Show |
1 | a0001c0001t0015g0081 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.258+4727_258+4728i others(14): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799870 | ||||||
chr5:88799870
|
T | TCATACAC others(7): Show |
1 | a0001c0001t0036g0015 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.258+4727_258+4728i others(16): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799870 | ||||||
chr5:88799870
|
TCA | T | 55 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0029others(52): Show | 55 | HG00099.hp2 HG00544.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.258+4726_258+4727d others(4): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799870 | ||||||
chr5:88799870
|
TCACA | T | 12 | a0001c0001t0002g0021a0001c0001t0002g0030a0001c0001t0002g0042others(9): Show | 12 | HG01515.hp1 HG01517.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.258+4724_258+4727d others(6): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799870 | ||||||
chr5:88799870
|
TCACACA | T | 11 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0002g0048others(8): Show | 11 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.258+4722_258+4727d others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799870 | ||||||
chr5:88799871
|
C | CAT | 3 | a0001c0001t0002g0003a0001c0001t0004g0164a0001c0001t0024g0066 | 3 | HG00323.hp1 HG02723.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.258+4726_258+4727i others(4): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799871 | ||||||
chr5:88799872
|
A | T | 1 | a0001c0001t0001g0181 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.258+4726T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799872 | ||||||
chr5:88799873
|
C | T | 164 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(161): Show | 164 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.258+4725G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799873 | ||||||
chr5:88799875
|
C | T | 32 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0029others(29): Show | 32 | HG00544.hp1 HG01069.hp1 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.258+4723G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799875 | ||||||
chr5:88799877
|
C | T | 8 | a0001c0001t0002g0021a0001c0001t0002g0030a0001c0001t0002g0042others(5): Show | 8 | HG01515.hp1 HG01517.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.258+4721G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799877 | ||||||
chr5:88799879
|
C | T | 8 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0002g0048others(5): Show | 8 | HG02486.hp2 NA18953.hp1 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.258+4719G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799879 | ||||||
chr5:88799901
|
CACACACA others(9): Show |
C | 1 | a0001c0001t0003g0091 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.258+4681_258+4696d others(18): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799901 | ||||||
chr5:88799903
|
CACACACA others(7): Show |
C | 3 | a0001c0001t0007g0016a0001c0001t0007g0017a0001c0001t0007g0018 | 3 | HG02896.hp1 HG02897.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.258+4681_258+4694d others(16): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799903 | ||||||
chr5:88799905
|
CACACACA others(5): Show |
C | 9 | a0001c0001t0001g0061a0001c0001t0001g0116a0001c0001t0001g0123others(6): Show | 9 | HG00280.hp2 HG01070.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.258+4681_258+4692d others(14): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799905 | ||||||
chr5:88799905
|
CACACACA others(7): Show |
C | 7 | a0001c0001t0004g0082a0001c0001t0004g0086a0001c0001t0004g0087others(4): Show | 7 | HG01496.hp1 HG01884.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.258+4679_258+4692d others(16): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799905 | ||||||
chr5:88799907
|
CACACACA others(3): Show |
C | 6 | a0001c0001t0001g0090a0001c0001t0001g0181a0001c0001t0006g0148others(3): Show | 6 | HG01884.hp1 HG02735.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.258+4681_258+4690d others(12): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799907 | ||||||
chr5:88799909
|
CACACAGA others(1): Show |
C | 49 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0063others(46): Show | 49 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.258+4681_258+4688d others(10): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799909 | ||||||
chr5:88799909
|
CACACAGA others(3): Show |
C | 4 | a0001c0001t0005g0083a0001c0001t0006g0133a0001c0001t0006g0134others(1): Show | 4 | HG02572.hp2 HG02970.hp1 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+4679_258+4688d others(12): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799909 | ||||||
chr5:88799911
|
CACAGAG | C | 22 | a0001c0001t0001g0001a0001c0001t0001g0064a0001c0001t0001g0075others(19): Show | 22 | HG00099.hp1 HG00673.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.258+4681_258+4686d others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799911 | ||||||
chr5:88799911
|
CACAGAGA others(1): Show |
C | 4 | a0001c0001t0002g0049a0001c0001t0004g0111a0001c0001t0004g0112others(1): Show | 4 | HG02451.hp1 HG03669.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+4679_258+4686d others(10): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799911 | ||||||
chr5:88799913
|
C | G | 5 | a0001c0001t0002g0062a0001c0001t0005g0013a0001c0001t0005g0014others(2): Show | 5 | HG01243.hp1 HG02559.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.258+4685G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799913 | ||||||
chr5:88799913
|
CAG | C | 30 | a0001c0001t0002g0007a0001c0001t0002g0023a0001c0001t0002g0102others(27): Show | 30 | HG00597.hp1 HG01123.hp2 HG01433.hp1 others(27): Show |
intron_variant | MODIFIER | c.258+4683_258+4684d others(4): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799913 | ||||||
chr5:88799913
|
CAGAG | C | 15 | a0001c0001t0001g0072a0001c0001t0001g0078a0001c0001t0001g0110others(12): Show | 15 | HG00639.hp2 HG01169.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.258+4681_258+4684d others(6): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799913 | ||||||
chr5:88799913
|
CAGAGAG | C | 3 | a0001c0001t0001g0039a0001c0001t0002g0020a0001c0001t0004g0115 | 3 | HG02109.hp2 NA19004.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.258+4679_258+4684d others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799913 | ||||||
chr5:88799915
|
G | C | 15 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0045others(12): Show | 15 | HG00280.hp1 HG00323.hp1 HG02818.hp2 others(12): Show |
intron_variant | MODIFIER | c.258+4683C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799915 | ||||||
chr5:88799917
|
G | C | 11 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0045others(8): Show | 11 | HG00280.hp1 HG01123.hp2 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.258+4681C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799917 | ||||||
chr5:88799919
|
G | C | 13 | a0001c0001t0001g0110a0001c0001t0002g0034a0001c0001t0002g0046others(10): Show | 13 | HG00639.hp2 HG01123.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.258+4679C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799919 | ||||||
chr5:88799968
|
C | T | 135 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(132): Show | 135 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.258+4630G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88799968 | ||||||
chr5:88800043
|
G | C | 4 | a0001c0001t0003g0091a0001c0001t0007g0016a0001c0001t0007g0017others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+4555C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88800043 | ||||||
chr5:88800509
|
G | T | 1 | a0001c0001t0002g0216 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.258+4089C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88800509 | ||||||
chr5:88800647
|
G | C | 1 | a0001c0001t0002g0206 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.258+3951C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88800647 | ||||||
chr5:88800858
|
T | A | 1 | a0001c0001t0001g0154 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.258+3740A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88800858 | ||||||
chr5:88801494
|
CT | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(133): Show | 136 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.258+3103delA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88801494 | ||||||
chr5:88801511
|
G | A | 8 | a0001c0001t0004g0108a0001c0001t0007g0300a0001c0001t0007g0301others(5): Show | 8 | HG00639.hp1 HG02055.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.258+3087C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88801511 | ||||||
chr5:88801519
|
G | A | 2 | a0001c0001t0002g0044a0001c0001t0002g0174 | 2 | HG01069.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.258+3079C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88801519 | ||||||
chr5:88801531
|
C | T | 4 | a0001c0001t0003g0091a0001c0001t0007g0016a0001c0001t0007g0017others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+3067G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88801531 | ||||||
chr5:88801585
|
C | T | 1 | a0001c0001t0002g0127 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.258+3013G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88801585 | ||||||
chr5:88801606
|
C | T | 2 | a0001c0001t0004g0108a0001c0001t0030g0109 | 2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.258+2992G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88801606 | ||||||
chr5:88801699
|
G | A | 1 | a0001c0001t0020g0004 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.258+2899C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88801699 | ||||||
chr5:88801878
|
T | C | 1 | a0001c0001t0003g0276 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.258+2720A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88801878 | ||||||
chr5:88802057
|
C | A | 1 | a0001c0001t0004g0002 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.258+2541G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88802057 | ||||||
chr5:88802219
|
C | A | 1 | a0001c0001t0001g0158 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.258+2379G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88802219 | ||||||
chr5:88802239
|
A | G | 7 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(4): Show | 7 | HG01891.hp2 HG02257.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.258+2359T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88802239 | ||||||
chr5:88802247
|
A | T | 159 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0036others(156): Show | 159 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(156): Show |
intron_variant | MODIFIER | c.258+2351T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88802247 | ||||||
chr5:88802265
|
C | T | 1 | a0001c0001t0004g0071 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.258+2333G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88802265 | ||||||
chr5:88802303
|
A | G | 166 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(163): Show | 166 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(163): Show |
intron_variant | MODIFIER | c.258+2295T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88802303 | ||||||
chr5:88802308
|
T | C | 1 | a0001c0001t0001g0065 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.258+2290A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88802308 | ||||||
chr5:88802444
|
T | G | 1 | a0001c0001t0001g0139 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.258+2154A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88802444 | ||||||
chr5:88802556
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.258+2042G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88802556 | ||||||
chr5:88802622
|
T | A | 2 | a0001c0001t0003g0238a0001c0001t0003g0266 | 2 | HG01099.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.258+1976A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88802622 | ||||||
chr5:88802728
|
T | C | 170 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(167): Show | 170 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(167): Show |
intron_variant | MODIFIER | c.258+1870A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88802728 | ||||||
chr5:88802749
|
A | G | 3 | a0001c0001t0004g0100a0001c0001t0004g0195a0001c0001t0004g0196 | 3 | HG01243.hp2 HG01361.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.258+1849T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88802749 | ||||||
chr5:88803129
|
T | A | 3 | a0001c0001t0002g0127a0001c0001t0002g0128a0001c0001t0025g0153 | 3 | HG02622.hp1 NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.258+1469A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88803129 | ||||||
chr5:88803140
|
T | C | 2 | a0001c0001t0002g0243a0001c0001t0002g0244 | 2 | HG03209.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.258+1458A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88803140 | ||||||
chr5:88803179
|
G | A | 1 | a0001c0001t0003g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.258+1419C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88803179 | ||||||
chr5:88803300
|
C | T | 4 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(1): Show | 4 | HG01168.hp2 HG01169.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+1298G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88803300 | ||||||
chr5:88803621
|
G | T | 2 | a0001c0001t0001g0029a0001c0001t0003g0025 | 2 | NA19075.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.258+977C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88803621 | ||||||
chr5:88803854
|
T | C | 71 | a0001c0001t0001g0267a0001c0001t0001g0273a0001c0001t0002g0234others(68): Show | 71 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.258+744A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88803854 | ||||||
chr5:88803972
|
C | T | 2 | a0001c0001t0002g0026a0001c0001t0002g0027 | 2 | HG03834.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.258+626G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88803972 | ||||||
chr5:88804134
|
G | C | 76 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0036others(73): Show | 76 | HG00544.hp1 HG00597.hp1 HG01069.hp1 others(73): Show |
intron_variant | MODIFIER | c.258+464C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88804134 | ||||||
chr5:88804209
|
G | A | 4 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0050others(1): Show | 4 | HG01123.hp2 HG01496.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+389C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88804209 | ||||||
chr5:88804210
|
G | C | 1 | a0001c0001t0012g0057 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.258+388C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88804210 | ||||||
chr5:88804443
|
A | C | 33 | a0001c0001t0001g0267a0001c0001t0001g0273a0001c0001t0002g0268others(30): Show | 33 | HG01069.hp2 HG01070.hp2 HG01358.hp2 others(30): Show |
intron_variant | MODIFIER | c.258+155T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | 88804443 | ||||||
chr5:88804832
|
A | T | 1 | a0001c0001t0003g0296 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.55-31T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88804832 | ||||||
chr5:88804846
|
C | T | 2 | a0001c0001t0008g0035a0001c0001t0008g0069 | 2 | HG01433.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.55-45G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88804846 | ||||||
chr5:88805096
|
T | A | 1 | a0001c0001t0002g0193 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.55-295A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88805096 | ||||||
chr5:88805278
|
A | G | 1 | a0001c0001t0002g0193 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.55-477T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88805278 | ||||||
chr5:88805325
|
A | G | 166 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(163): Show | 166 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(163): Show |
intron_variant | MODIFIER | c.55-524T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88805325 | ||||||
chr5:88805333
|
C | T | 169 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(166): Show | 169 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(166): Show |
intron_variant | MODIFIER | c.55-532G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88805333 | ||||||
chr5:88805434
|
A | G | 13 | a0001c0001t0001g0065a0001c0001t0002g0021a0001c0001t0002g0030others(10): Show | 13 | HG01515.hp1 HG01517.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.55-633T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88805434 | ||||||
chr5:88805687
|
T | C | 1 | a0001c0001t0001g0029 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.55-886A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88805687 | ||||||
chr5:88805739
|
A | ATTTCACT others(1): Show |
8 | a0001c0001t0004g0108a0001c0001t0007g0300a0001c0001t0007g0301others(5): Show | 8 | HG00639.hp1 HG02055.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.55-946_55-939dupGA others(6): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88805739 | ||||||
chr5:88805772
|
T | A | 2 | a0001c0001t0015g0081a0001c0001t0015g0089 | 2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.55-971A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88805772 | ||||||
chr5:88805823
|
C | CT | 54 | a0001c0001t0001g0064a0001c0001t0001g0078a0001c0001t0001g0095others(51): Show | 54 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.55-1023dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88805823 | ||||||
chr5:88805823
|
C | CTT | 12 | a0001c0001t0001g0024a0001c0001t0001g0061a0001c0001t0001g0121others(9): Show | 12 | HG00323.hp2 HG00733.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.55-1024_55-1023dup others(2): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88805823 | ||||||
chr5:88805823
|
CT | C | 17 | a0001c0001t0001g0008a0001c0001t0002g0048a0001c0001t0002g0189others(14): Show | 17 | HG00099.hp2 HG01069.hp2 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.55-1023delA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88805823 | ||||||
chr5:88805823
|
CTT | C | 69 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0029others(66): Show | 69 | HG00544.hp1 HG00597.hp1 HG01069.hp1 others(66): Show |
intron_variant | MODIFIER | c.55-1024_55-1023del others(2): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88805823 | ||||||
chr5:88805871
|
A | G | 2 | a0001c0001t0004g0108a0001c0001t0030g0109 | 2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.55-1070T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88805871 | ||||||
chr5:88806030
|
A | G | 4 | a0001c0001t0003g0091a0001c0001t0007g0016a0001c0001t0007g0017others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.55-1229T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88806030 | ||||||
chr5:88806143
|
T | C | 1 | a0001c0001t0001g0142 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.55-1342A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88806143 | ||||||
chr5:88806265
|
C | T | 4 | a0001c0001t0003g0091a0001c0001t0007g0016a0001c0001t0007g0017others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.55-1464G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88806265 | ||||||
chr5:88806416
|
A | G | 11 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0077others(8): Show | 11 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.55-1615T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88806416 | ||||||
chr5:88806464
|
T | G | 85 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(82): Show | 85 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.55-1663A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88806464 | ||||||
chr5:88806739
|
A | AAAAATAT others(20): Show |
4 | a0001c0001t0002g0191a0001c0001t0004g0002a0001c0001t0019g0067others(1): Show | 4 | HG01891.hp2 HG03225.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.55-1965_55-1939dup others(27): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88806739 | ||||||
chr5:88806742
|
A | G | 1 | a0001c0001t0003g0051 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.55-1941T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88806742 | ||||||
chr5:88807046
|
T | C | 189 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(186): Show | 189 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(186): Show |
intron_variant | MODIFIER | c.55-2245A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88807046 | ||||||
chr5:88807200
|
T | C | 16 | a0001c0001t0003g0255a0001c0001t0004g0100a0001c0001t0004g0103others(13): Show | 16 | HG00741.hp1 HG01243.hp2 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.55-2399A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88807200 | ||||||
chr5:88807368
|
C | T | 3 | a0001c0001t0002g0191a0001c0001t0007g0300a0001c0001t0007g0301 | 3 | HG02572.hp1 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.55-2567G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88807368 | ||||||
chr5:88807396
|
T | C | 20 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0077others(17): Show | 20 | HG00639.hp2 HG00733.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.55-2595A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88807396 | ||||||
chr5:88807471
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.55-2670G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88807471 | ||||||
chr5:88807504
|
G | C | 3 | a0001c0001t0001g0031a0001c0001t0012g0138a0001c0001t0012g0151 | 3 | HG01255.hp2 HG01433.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.55-2703C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88807504 | ||||||
chr5:88807975
|
T | A | 6 | a0001c0001t0004g0086a0001c0001t0004g0087a0001c0001t0004g0088others(3): Show | 6 | HG01884.hp2 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.55-3174A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88807975 | ||||||
chr5:88808081
|
T | C | 2 | a0001c0001t0002g0243a0001c0001t0002g0244 | 2 | HG03209.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.55-3280A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88808081 | ||||||
chr5:88808442
|
T | C | 1 | a0001c0001t0004g0297 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.55-3641A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88808442 | ||||||
chr5:88808530
|
C | T | 4 | a0001c0001t0003g0091a0001c0001t0007g0016a0001c0001t0007g0017others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.55-3729G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88808530 | ||||||
chr5:88808543
|
A | G | 20 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0077others(17): Show | 20 | HG00639.hp2 HG00733.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.55-3742T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88808543 | ||||||
chr5:88808605
|
C | T | 20 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0077others(17): Show | 20 | HG00639.hp2 HG00733.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.55-3804G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88808605 | ||||||
chr5:88809289
|
A | G | 1 | a0001c0001t0003g0091 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.55-4488T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88809289 | ||||||
chr5:88809458
|
A | G | 2 | a0001c0001t0015g0081a0001c0001t0015g0089 | 2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.55-4657T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88809458 | ||||||
chr5:88809644
|
T | G | 2 | a0001c0001t0004g0136a0001c0001t0004g0164 | 2 | HG00280.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.55-4843A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88809644 | ||||||
chr5:88809683
|
C | A | 1 | a0001c0001t0002g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.55-4882G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88809683 | ||||||
chr5:88809730
|
C | T | 1 | a0001c0001t0020g0004 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.55-4929G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88809730 | ||||||
chr5:88809797
|
C | T | 190 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(187): Show | 190 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(187): Show |
intron_variant | MODIFIER | c.55-4996G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88809797 | ||||||
chr5:88810284
|
T | C | 1 | a0001c0001t0007g0301 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.55-5483A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88810284 | ||||||
chr5:88810441
|
T | C | 190 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(187): Show | 190 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(187): Show |
intron_variant | MODIFIER | c.55-5640A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88810441 | ||||||
chr5:88810533
|
CA | C | 188 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(185): Show | 188 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(185): Show |
intron_variant | MODIFIER | c.55-5733delT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88810533 | ||||||
chr5:88810942
|
T | G | 1 | a0001c0001t0002g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.55-6141A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88810942 | ||||||
chr5:88811036
|
C | G | 8 | a0001c0001t0001g0110a0001c0001t0002g0023a0001c0001t0003g0113others(5): Show | 8 | HG00639.hp2 HG01192.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.55-6235G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88811036 | ||||||
chr5:88811084
|
A | G | 1 | a0001c0001t0032g0130 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.55-6283T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88811084 | ||||||
chr5:88811520
|
C | A | 85 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(82): Show | 85 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.55-6719G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88811520 | ||||||
chr5:88811752
|
A | G | 1 | a0001c0001t0002g0021 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.55-6951T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88811752 | ||||||
chr5:88811791
|
T | C | 13 | a0001c0001t0001g0065a0001c0001t0002g0021a0001c0001t0002g0030others(10): Show | 13 | HG01515.hp1 HG01517.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.55-6990A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88811791 | ||||||
chr5:88811985
|
T | G | 2 | a0001c0001t0002g0102a0001c0001t0002g0132 | 2 | NA19065.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.55-7184A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88811985 | ||||||
chr5:88812610
|
TC | T | 73 | a0001c0001t0001g0267a0001c0001t0001g0273a0001c0001t0002g0212others(70): Show | 73 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.55-7810delG | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88812610 | ||||||
chr5:88812636
|
T | A | 175 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(172): Show | 175 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(172): Show |
intron_variant | MODIFIER | c.55-7835A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88812636 | ||||||
chr5:88812757
|
G | A | 175 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(172): Show | 175 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(172): Show |
intron_variant | MODIFIER | c.55-7956C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88812757 | ||||||
chr5:88813065
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.55-8264C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88813065 | ||||||
chr5:88813471
|
A | T | 2 | a0001c0001t0007g0017a0001c0001t0007g0018 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.55-8670T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88813471 | ||||||
chr5:88813509
|
C | A | 1 | a0001c0001t0001g0092 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.55-8708G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88813509 | ||||||
chr5:88813773
|
C | A | 19 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0077others(16): Show | 19 | HG00639.hp2 HG00733.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.55-8972G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88813773 | ||||||
chr5:88814267
|
C | T | 171 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(168): Show | 171 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(168): Show |
intron_variant | MODIFIER | c.55-9466G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88814267 | ||||||
chr5:88814276
|
T | C | 3 | a0001c0001t0001g0097a0001c0001t0001g0142a0001c0001t0001g0143 | 3 | HG02027.hp2 NA18959.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.54+9459A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88814276 | ||||||
chr5:88814521
|
A | G | 171 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(168): Show | 171 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(168): Show |
intron_variant | MODIFIER | c.54+9214T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88814521 | ||||||
chr5:88814546
|
C | T | 269 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(266): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.54+9189G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88814546 | ||||||
chr5:88814573
|
C | A | 13 | a0001c0001t0001g0065a0001c0001t0002g0021a0001c0001t0002g0030others(10): Show | 13 | HG01515.hp1 HG01517.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.54+9162G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88814573 | ||||||
chr5:88815391
|
C | T | 1 | a0001c0001t0035g0085 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.54+8344G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88815391 | ||||||
chr5:88815392
|
C | G | 269 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(266): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.54+8343G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88815392 | ||||||
chr5:88815527
|
G | C | 10 | a0001c0001t0002g0186a0001c0001t0002g0191a0001c0001t0002g0192others(7): Show | 10 | HG02145.hp2 HG02818.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.54+8208C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88815527 | ||||||
chr5:88815587
|
T | G | 1 | a0001c0001t0002g0188 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.54+8148A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88815587 | ||||||
chr5:88815932
|
G | A | 2 | a0001c0001t0001g0104a0001c0001t0001g0105 | 2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.54+7803C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88815932 | ||||||
chr5:88816126
|
A | G | 2 | a0001c0001t0015g0081a0001c0001t0015g0089 | 2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.54+7609T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88816126 | ||||||
chr5:88816229
|
C | T | 1 | a0001c0001t0010g0056 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.54+7506G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88816229 | ||||||
chr5:88816303
|
G | A | 1 | a0001c0001t0003g0271 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.54+7432C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88816303 | ||||||
chr5:88816406
|
G | A | 1 | a0001c0001t0003g0257 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.54+7329C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88816406 | ||||||
chr5:88816411
|
T | G | 1 | a0001c0001t0003g0051 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.54+7324A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88816411 | ||||||
chr5:88816465
|
C | CT | 12 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0142others(9): Show | 12 | HG00741.hp2 HG02027.hp2 HG02602.hp2 others(9): Show |
intron_variant | MODIFIER | c.54+7269dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88816465 | ||||||
chr5:88816465
|
CT | C | 79 | a0001c0001t0001g0031a0001c0001t0001g0065a0001c0001t0001g0090others(76): Show | 79 | HG00323.hp1 HG00597.hp1 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.54+7269delA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88816465 | ||||||
chr5:88816465
|
CTT | C | 70 | a0001c0001t0001g0267a0001c0001t0001g0273a0001c0001t0002g0043others(67): Show | 70 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(67): Show |
intron_variant | MODIFIER | c.54+7268_54+7269del others(2): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88816465 | ||||||
chr5:88816596
|
C | T | 13 | a0001c0001t0004g0082a0001c0001t0004g0208a0001c0001t0004g0256others(10): Show | 13 | HG01496.hp1 HG02055.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.54+7139G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88816596 | ||||||
chr5:88816708
|
T | C | 1 | a0001c0001t0004g0297 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.54+7027A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88816708 | ||||||
chr5:88816864
|
C | T | 3 | a0001c0001t0004g0086a0001c0001t0004g0087a0001c0001t0004g0088 | 3 | HG01884.hp2 HG02280.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.54+6871G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88816864 | ||||||
chr5:88816934
|
C | A | 1 | a0001c0001t0020g0004 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.54+6801G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88816934 | ||||||
chr5:88816944
|
T | A | 7 | a0001c0001t0001g0110a0001c0001t0003g0113a0001c0001t0004g0011others(4): Show | 7 | HG00639.hp2 HG01192.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.54+6791A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88816944 | ||||||
chr5:88817008
|
C | T | 13 | a0001c0001t0001g0065a0001c0001t0002g0021a0001c0001t0002g0030others(10): Show | 13 | HG01515.hp1 HG01517.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.54+6727G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88817008 | ||||||
chr5:88817034
|
C | CA | 4 | a0001c0001t0001g0031a0001c0001t0012g0057a0001c0001t0012g0138others(1): Show | 4 | HG01099.hp1 HG01255.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.54+6700dupT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88817034 | ||||||
chr5:88817218
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.54+6517C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88817218 | ||||||
chr5:88817411
|
C | T | 7 | a0001c0001t0001g0110a0001c0001t0003g0113a0001c0001t0004g0011others(4): Show | 7 | HG00639.hp2 HG01192.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.54+6324G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88817411 | ||||||
chr5:88817438
|
T | C | 5 | a0001c0001t0004g0297a0001c0001t0005g0013a0001c0001t0005g0014others(2): Show | 5 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.54+6297A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88817438 | ||||||
chr5:88817646
|
C | A | 1 | a0001c0001t0001g0092 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.54+6089G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88817646 | ||||||
chr5:88817842
|
C | G | 13 | a0001c0001t0002g0234a0001c0001t0003g0233a0001c0001t0003g0235others(10): Show | 13 | HG00099.hp2 HG00642.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.54+5893G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88817842 | ||||||
chr5:88817912
|
A | G | 1 | a0001c0001t0001g0092 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.54+5823T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88817912 | ||||||
chr5:88818235
|
A | C | 4 | a0001c0001t0005g0013a0001c0001t0005g0014a0001c0001t0005g0298others(1): Show | 4 | HG01243.hp1 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.54+5500T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88818235 | ||||||
chr5:88818447
|
G | C | 1 | a0001c0001t0001g0038 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.54+5288C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88818447 | ||||||
chr5:88818659
|
T | C | 171 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(168): Show | 171 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(168): Show |
intron_variant | MODIFIER | c.54+5076A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88818659 | ||||||
chr5:88818727
|
G | A | 9 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0063others(6): Show | 9 | HG01358.hp1 NA18979.hp1 NA18985.hp1 others(6): Show |
intron_variant | MODIFIER | c.54+5008C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88818727 | ||||||
chr5:88818737
|
G | T | 2 | a0001c0001t0004g0108a0001c0001t0030g0109 | 2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.54+4998C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88818737 | ||||||
chr5:88818885
|
A | C | 2 | a0001c0001t0019g0067a0001c0001t0024g0066 | 2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.54+4850T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88818885 | ||||||
chr5:88818979
|
C | T | 1 | a0001c0001t0004g0297 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.54+4756G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88818979 | ||||||
chr5:88819056
|
G | A | 13 | a0001c0001t0001g0065a0001c0001t0002g0021a0001c0001t0002g0030others(10): Show | 13 | HG01515.hp1 HG01517.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.54+4679C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88819056 | ||||||
chr5:88819361
|
C | T | 13 | a0001c0001t0001g0065a0001c0001t0002g0021a0001c0001t0002g0030others(10): Show | 13 | HG01515.hp1 HG01517.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.54+4374G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88819361 | ||||||
chr5:88819425
|
A | G | 2 | a0001c0001t0004g0108a0001c0001t0030g0109 | 2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.54+4310T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88819425 | ||||||
chr5:88819477
|
C | T | 1 | a0001c0001t0003g0237 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.54+4258G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88819477 | ||||||
chr5:88819816
|
C | T | 5 | a0001c0001t0002g0213a0001c0001t0005g0013a0001c0001t0005g0014others(2): Show | 5 | HG01243.hp1 HG02559.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.54+3919G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88819816 | ||||||
chr5:88820068
|
T | A | 175 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(172): Show | 175 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(172): Show |
intron_variant | MODIFIER | c.54+3667A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88820068 | ||||||
chr5:88820075
|
TTA | T | 172 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(169): Show | 172 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(169): Show |
intron_variant | MODIFIER | c.54+3658_54+3659del others(2): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88820075 | ||||||
chr5:88820499
|
T | C | 1 | a0001c0001t0004g0103 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.54+3236A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88820499 | ||||||
chr5:88820502
|
C | T | 76 | a0001c0001t0001g0267a0001c0001t0001g0273a0001c0001t0002g0234others(73): Show | 76 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.54+3233G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88820502 | ||||||
chr5:88820520
|
T | C | 1 | a0001c0001t0033g0060 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.54+3215A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88820520 | ||||||
chr5:88820533
|
G | C | 2 | a0001c0001t0019g0067a0001c0001t0024g0066 | 2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.54+3202C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88820533 | ||||||
chr5:88820560
|
A | T | 1 | a0001c0001t0004g0100 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.54+3175T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88820560 | ||||||
chr5:88820588
|
T | C | 4 | a0001c0001t0001g0031a0001c0001t0012g0057a0001c0001t0012g0138others(1): Show | 4 | HG01099.hp1 HG01255.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.54+3147A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88820588 | ||||||
chr5:88820711
|
C | T | 19 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0077others(16): Show | 19 | HG00639.hp2 HG00733.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.54+3024G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88820711 | ||||||
chr5:88820787
|
G | A | 2 | a0001c0001t0004g0108a0001c0001t0030g0109 | 2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.54+2948C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88820787 | ||||||
chr5:88820853
|
C | A | 2 | a0001c0001t0004g0108a0001c0001t0030g0109 | 2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.54+2882G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88820853 | ||||||
chr5:88821210
|
A | T | 174 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(171): Show | 174 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(171): Show |
intron_variant | MODIFIER | c.54+2525T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88821210 | ||||||
chr5:88821259
|
T | C | 1 | a0001c0001t0002g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.54+2476A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88821259 | ||||||
chr5:88821260
|
T | G | 2 | a0001c0001t0001g0126a0001c0001t0001g0154 | 2 | NA19001.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.54+2475A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88821260 | ||||||
chr5:88821332
|
T | C | 1 | a0001c0001t0001g0190 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.54+2403A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88821332 | ||||||
chr5:88821677
|
C | T | 6 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(3): Show | 6 | HG02145.hp2 HG02257.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.54+2058G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88821677 | ||||||
chr5:88821703
|
T | A | 1 | a0001c0001t0004g0297 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.54+2032A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88821703 | ||||||
chr5:88821704
|
A | T | 9 | a0001c0001t0006g0133a0001c0001t0006g0134a0001c0001t0006g0148others(6): Show | 9 | HG01928.hp1 NA18941.hp1 NA18945.hp1 others(6): Show |
intron_variant | MODIFIER | c.54+2031T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88821704 | ||||||
chr5:88821800
|
G | C | 1 | a0001c0001t0003g0249 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.54+1935C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88821800 | ||||||
chr5:88822271
|
C | T | 2 | a0001c0001t0015g0081a0001c0001t0015g0089 | 2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.54+1464G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88822271 | ||||||
chr5:88822577
|
G | A | 1 | a0001c0001t0002g0191 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.54+1158C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88822577 | ||||||
chr5:88822603
|
T | G | 2 | a0001c0001t0002g0234a0001c0001t0003g0251 | 2 | HG02602.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.54+1132A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88822603 | ||||||
chr5:88822778
|
G | A | 1 | a0001c0001t0002g0062 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.54+957C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88822778 | ||||||
chr5:88822837
|
C | T | 1 | a0001c0001t0034g0012 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.54+898G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88822837 | ||||||
chr5:88822964
|
C | A | 2 | a0001c0001t0002g0243a0001c0001t0002g0244 | 2 | HG03209.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.54+771G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88822964 | ||||||
chr5:88823041
|
A | G | 171 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(168): Show | 171 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(168): Show |
intron_variant | MODIFIER | c.54+694T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88823041 | ||||||
chr5:88823562
|
T | C | 2 | a0001c0001t0007g0300a0001c0001t0007g0301 | 2 | HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.54+173A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 2/10 | chr5 | 88823562 | ||||||
chr5:88823968
|
C | T | 1 | a0001c0001t0002g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-142-38G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88823968 | ||||||
chr5:88824262
|
C | CCT | 170 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(167): Show | 170 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(167): Show |
intron_variant | MODIFIER | c.-142-333_-142-332i others(4): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88824262 | ||||||
chr5:88824509
|
C | T | 2 | a0001c0001t0003g0237a0001c0001t0037g0236 | 2 | HG01168.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-142-579G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88824509 | ||||||
chr5:88824599
|
T | C | 171 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(168): Show | 171 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(168): Show |
intron_variant | MODIFIER | c.-142-669A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88824599 | ||||||
chr5:88825089
|
C | A | 1 | a0001c0001t0034g0012 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-142-1159G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88825089 | ||||||
chr5:88825231
|
T | C | 1 | a0001c0001t0001g0063 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-142-1301A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88825231 | ||||||
chr5:88825240
|
T | G | 1 | a0001c0001t0003g0185 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-142-1310A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88825240 | ||||||
chr5:88825265
|
AT | A | 7 | a0001c0001t0001g0125a0001c0001t0001g0146a0001c0001t0001g0171others(4): Show | 7 | HG01496.hp2 HG02129.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-142-1336delA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88825265 | ||||||
chr5:88825371
|
T | A | 171 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(168): Show | 171 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(168): Show |
intron_variant | MODIFIER | c.-142-1441A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88825371 | ||||||
chr5:88825839
|
G | A | 1 | a0001c0001t0003g0258 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-142-1909C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88825839 | ||||||
chr5:88826361
|
C | A | 34 | a0001c0001t0002g0182a0001c0001t0002g0183a0001c0001t0002g0186others(31): Show | 34 | HG00597.hp1 HG01433.hp1 HG01975.hp2 others(31): Show |
intron_variant | MODIFIER | c.-142-2431G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88826361 | ||||||
chr5:88826383
|
A | T | 2 | a0001c0001t0003g0252a0001c0001t0004g0246 | 2 | HG00642.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.-142-2453T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88826383 | ||||||
chr5:88826416
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-142-2486G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88826416 | ||||||
chr5:88826908
|
T | A | 1 | a0001c0001t0001g0024 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-142-2978A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88826908 | ||||||
chr5:88826908
|
T | TA | 116 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(113): Show | 116 | HG00597.hp1 HG00639.hp1 HG00639.hp2 others(113): Show |
intron_variant | MODIFIER | c.-142-2979dupT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88826908 | ||||||
chr5:88827523
|
T | A | 1 | a0001c0001t0004g0297 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-142-3593A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88827523 | ||||||
chr5:88827608
|
A | C | 1 | a0001c0001t0003g0254 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-142-3678T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88827608 | ||||||
chr5:88827653
|
T | C | 1 | a0001c0001t0025g0153 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-142-3723A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88827653 | ||||||
chr5:88827733
|
T | A | 73 | a0001c0001t0001g0267a0001c0001t0001g0273a0001c0001t0002g0234others(70): Show | 73 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.-142-3803A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88827733 | ||||||
chr5:88827912
|
A | G | 3 | a0001c0001t0002g0048a0001c0001t0003g0041a0001c0001t0003g0051 | 3 | NA18955.hp1 NA18966.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.-142-3982T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88827912 | ||||||
chr5:88827914
|
T | TA | 124 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(121): Show | 124 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(121): Show |
intron_variant | MODIFIER | c.-142-3985dupT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88827914 | ||||||
chr5:88828029
|
T | A | 1 | a0001c0001t0002g0182 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-142-4099A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88828029 | ||||||
chr5:88828306
|
T | G | 175 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(172): Show | 175 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(172): Show |
intron_variant | MODIFIER | c.-142-4376A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88828306 | ||||||
chr5:88828399
|
T | A | 1 | a0001c0001t0002g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-142-4469A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88828399 | ||||||
chr5:88828441
|
A | G | 3 | a0001c0001t0001g0101a0001c0001t0004g0099a0001c0001t0004g0103 | 3 | HG01891.hp1 HG02818.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-142-4511T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88828441 | ||||||
chr5:88828511
|
C | T | 3 | a0001c0001t0003g0254a0001c0001t0003g0260a0001c0001t0003g0294 | 3 | NA18999.hp2 NA19074.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.-142-4581G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88828511 | ||||||
chr5:88828850
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-142-4920G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88828850 | ||||||
chr5:88829112
|
C | T | 1 | a0001c0001t0002g0232 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-142-5182G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88829112 | ||||||
chr5:88829206
|
T | C | 1 | a0001c0001t0003g0231 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-142-5276A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88829206 | ||||||
chr5:88829413
|
T | G | 11 | a0001c0001t0004g0108a0001c0001t0004g0297a0001c0001t0005g0013others(8): Show | 11 | HG00639.hp1 HG01243.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.-142-5483A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88829413 | ||||||
chr5:88829518
|
C | T | 1 | a0001c0001t0002g0232 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-142-5588G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88829518 | ||||||
chr5:88829676
|
G | A | 4 | a0001c0001t0003g0091a0001c0001t0007g0016a0001c0001t0007g0017others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-142-5746C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88829676 | ||||||
chr5:88829677
|
C | G | 4 | a0001c0001t0003g0091a0001c0001t0007g0016a0001c0001t0007g0017others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-142-5747G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88829677 | ||||||
chr5:88830036
|
T | G | 160 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(157): Show | 160 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(157): Show |
intron_variant | MODIFIER | c.-142-6106A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88830036 | ||||||
chr5:88830522
|
T | C | 3 | a0001c0001t0004g0100a0001c0001t0004g0195a0001c0001t0004g0196 | 3 | HG01243.hp2 HG01361.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-142-6592A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88830522 | ||||||
chr5:88830624
|
T | C | 1 | a0001c0001t0002g0182 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-142-6694A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88830624 | ||||||
chr5:88831100
|
C | T | 1 | a0001c0001t0003g0169 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-142-7170G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88831100 | ||||||
chr5:88831386
|
T | C | 7 | a0001c0001t0001g0061a0001c0001t0001g0123a0001c0001t0001g0135others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.-142-7456A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88831386 | ||||||
chr5:88831529
|
T | C | 1 | a0001c0001t0002g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-142-7599A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88831529 | ||||||
chr5:88831607
|
T | C | 15 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0077others(12): Show | 15 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.-142-7677A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88831607 | ||||||
chr5:88831611
|
T | C | 5 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(2): Show | 5 | HG02257.hp2 HG02486.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-142-7681A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88831611 | ||||||
chr5:88832109
|
C | T | 2 | a0001c0001t0001g0121a0001c0001t0001g0140 | 2 | HG00544.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.-142-8179G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88832109 | ||||||
chr5:88832219
|
A | G | 4 | a0001c0001t0003g0091a0001c0001t0007g0016a0001c0001t0007g0017others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-142-8289T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88832219 | ||||||
chr5:88832732
|
T | C | 1 | a0001c0001t0030g0109 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-142-8802A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88832732 | ||||||
chr5:88832737
|
C | T | 3 | a0001c0001t0002g0127a0001c0001t0002g0128a0001c0001t0025g0153 | 3 | HG02622.hp1 NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-142-8807G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88832737 | ||||||
chr5:88832762
|
G | A | 2 | a0001c0001t0001g0101a0001c0001t0004g0099 | 2 | HG02818.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-142-8832C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88832762 | ||||||
chr5:88832825
|
A | T | 266 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(263): Show | 266 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.-142-8895T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88832825 | ||||||
chr5:88832835
|
G | T | 266 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(263): Show | 266 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.-142-8905C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88832835 | ||||||
chr5:88832874
|
T | A | 3 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0035g0085 | 3 | HG02055.hp1 HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-142-8944A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88832874 | ||||||
chr5:88832875
|
G | T | 3 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0035g0085 | 3 | HG02055.hp1 HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-142-8945C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88832875 | ||||||
chr5:88833516
|
C | T | 3 | a0001c0001t0002g0200a0001c0001t0002g0201a0001c0001t0002g0202 | 3 | NA18969.hp1 NA19057.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.-142-9586G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88833516 | ||||||
chr5:88833517
|
G | A | 1 | a0001c0001t0008g0107 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-142-9587C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88833517 | ||||||
chr5:88833818
|
A | G | 3 | a0001c0001t0008g0035a0001c0001t0008g0068a0001c0001t0008g0069 | 3 | HG01433.hp1 HG01975.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.-142-9888T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88833818 | ||||||
chr5:88833894
|
G | A | 2 | a0001c0001t0001g0131a0001c0001t0001g0172 | 2 | HG00733.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.-142-9964C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88833894 | ||||||
chr5:88834075
|
TG | T | 44 | a0001c0001t0002g0182a0001c0001t0002g0183a0001c0001t0002g0187others(41): Show | 44 | HG00597.hp1 HG01433.hp1 HG01975.hp2 others(41): Show |
intron_variant | MODIFIER | c.-142-10146delC | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88834075 | ||||||
chr5:88834503
|
C | T | 10 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0077others(7): Show | 10 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-142-10573G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88834503 | ||||||
chr5:88834833
|
C | T | 10 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0077others(7): Show | 10 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-142-10903G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88834833 | ||||||
chr5:88834953
|
ATAT | A | 3 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0147 | 3 | NA18951.hp1 NA18960.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.-142-11026_-142-11 others(9): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88834953 | ||||||
chr5:88835307
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-142-11377G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88835307 | ||||||
chr5:88835308
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-142-11378G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88835308 | ||||||
chr5:88835465
|
G | T | 1 | a0001c0001t0001g0040 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-142-11535C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88835465 | ||||||
chr5:88835477
|
C | A | 7 | a0001c0001t0004g0082a0001c0001t0004g0086a0001c0001t0004g0087others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-142-11547G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88835477 | ||||||
chr5:88835610
|
G | A | 2 | a0001c0001t0014g0290a0001c0001t0014g0295 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-142-11680C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88835610 | ||||||
chr5:88835675
|
T | C | 2 | a0001c0001t0003g0242a0001c0001t0003g0245 | 2 | HG01261.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.-142-11745A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88835675 | ||||||
chr5:88835679
|
G | A | 1 | a0001c0001t0006g0150 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-142-11749C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88835679 | ||||||
chr5:88835813
|
T | TA | 145 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(142): Show | 145 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(142): Show |
intron_variant | MODIFIER | c.-142-11884dupT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88835813 | ||||||
chr5:88835813
|
T | TAA | 14 | a0001c0001t0001g0065a0001c0001t0002g0021a0001c0001t0002g0030others(11): Show | 14 | HG01433.hp1 HG01515.hp1 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.-142-11885_-142-11 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88835813 | ||||||
chr5:88835848
|
C | A | 2 | a0001c0001t0004g0108a0001c0001t0030g0109 | 2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-142-11918G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88835848 | ||||||
chr5:88836144
|
T | C | 2 | a0001c0001t0010g0032a0001c0001t0010g0033 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-142-12214A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88836144 | ||||||
chr5:88836819
|
G | T | 1 | a0001c0001t0002g0198 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-142-12889C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88836819 | ||||||
chr5:88837002
|
C | CA | 87 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0031others(84): Show | 87 | HG00280.hp1 HG00544.hp1 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.-142-13073dupT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88837002 | ||||||
chr5:88837002
|
C | CAA | 73 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0090others(70): Show | 73 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.-142-13074_-142-13 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88837002 | ||||||
chr5:88837002
|
C | CAAA | 14 | a0001c0001t0001g0139a0001c0001t0001g0143a0001c0001t0001g0159others(11): Show | 14 | HG00323.hp2 HG01255.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-142-13075_-142-13 others(9): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88837002 | ||||||
chr5:88837002
|
CA | C | 10 | a0001c0001t0002g0030a0001c0001t0002g0200a0001c0001t0002g0234others(7): Show | 10 | HG00639.hp1 HG01891.hp2 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.-142-13073delT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88837002 | ||||||
chr5:88837002
|
CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0002g0187a0001c0001t0002g0188 | 2 | HG02148.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.-142-13083_-142-13 others(17): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88837002 | ||||||
chr5:88837101
|
A | G | 4 | a0001c0001t0005g0013a0001c0001t0005g0014a0001c0001t0034g0012others(1): Show | 4 | HG00639.hp1 HG01243.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-142-13171T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88837101 | ||||||
chr5:88837452
|
T | C | 7 | a0001c0001t0004g0082a0001c0001t0004g0086a0001c0001t0004g0087others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-142-13522A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88837452 | ||||||
chr5:88837590
|
C | G | 1 | a0001c0001t0003g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-142-13660G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88837590 | ||||||
chr5:88837781
|
C | T | 1 | a0001c0001t0002g0028 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-142-13851G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88837781 | ||||||
chr5:88837820
|
T | C | 3 | a0001c0001t0003g0262a0001c0001t0003g0265a0001c0001t0003g0272 | 3 | NA18965.hp1 NA19063.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-142-13890A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88837820 | ||||||
chr5:88838068
|
G | A | 1 | a0001c0001t0007g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-142-14138C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88838068 | ||||||
chr5:88838102
|
A | G | 264 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(261): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.-142-14172T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88838102 | ||||||
chr5:88838296
|
G | A | 1 | a0001c0001t0001g0064 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-142-14366C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88838296 | ||||||
chr5:88838377
|
GT | G | 6 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(3): Show | 6 | HG02257.hp2 HG02486.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-142-14448delA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88838377 | ||||||
chr5:88838493
|
A | G | 169 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(166): Show | 169 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(166): Show |
intron_variant | MODIFIER | c.-142-14563T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88838493 | ||||||
chr5:88838695
|
C | A | 1 | a0001c0001t0004g0100 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-142-14765G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88838695 | ||||||
chr5:88839321
|
A | ATC | 6 | a0001c0001t0001g0097a0001c0001t0001g0104a0001c0001t0001g0105others(3): Show | 6 | HG02027.hp2 HG03669.hp1 HG04204.hp1 others(3): Show |
intron_variant | MODIFIER | c.-142-15393_-142-15 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839321 | ||||||
chr5:88839321
|
ATC | A | 67 | a0001c0001t0001g0061a0001c0001t0001g0093a0001c0001t0001g0094others(64): Show | 67 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.-142-15393_-142-15 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839321 | ||||||
chr5:88839347
|
C | CTCTATCT others(1): Show |
17 | a0001c0001t0001g0065a0001c0001t0002g0021a0001c0001t0002g0030others(14): Show | 17 | HG01243.hp1 HG01433.hp1 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.-142-15418_-142-15 others(14): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839347 | ||||||
chr5:88839351
|
C | A | 21 | a0001c0001t0001g0065a0001c0001t0001g0072a0001c0001t0001g0077others(18): Show | 21 | HG00099.hp2 HG01243.hp1 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.-142-15421G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839351 | ||||||
chr5:88839351
|
C | CTATCTA | 15 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(12): Show | 15 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.-142-15422_-142-15 others(12): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839351 | ||||||
chr5:88839351
|
C | CTATCTAT others(3): Show |
1 | a0001c0001t0034g0012 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-142-15422_-142-15 others(16): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839351 | ||||||
chr5:88839351
|
C | CTCTA | 3 | a0001c0001t0002g0192a0001c0001t0007g0300a0001c0001t0007g0301 | 3 | HG02572.hp1 NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-142-15425_-142-15 others(10): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839351 | ||||||
chr5:88839351
|
C | CTCTATCT others(1): Show |
63 | a0001c0001t0001g0110a0001c0001t0001g0267a0001c0001t0001g0273others(60): Show | 63 | HG00639.hp2 HG00642.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.-142-15429_-142-15 others(14): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839351 | ||||||
chr5:88839351
|
C | CTCTATCT others(5): Show |
2 | a0001c0001t0002g0023a0001c0001t0036g0015 | 2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-142-15433_-142-15 others(18): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839351 | ||||||
chr5:88839351
|
C | CTCTCTA | 21 | a0001c0001t0002g0182a0001c0001t0002g0183a0001c0001t0002g0198others(18): Show | 21 | HG00597.hp1 HG02132.hp2 HG02809.hp1 others(18): Show |
intron_variant | MODIFIER | c.-142-15422_-142-15 others(12): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839351 | ||||||
chr5:88839351
|
C | CTCTCTAT others(3): Show |
6 | a0001c0001t0003g0230a0001c0001t0003g0231a0001c0001t0004g0286others(3): Show | 6 | HG02486.hp1 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-142-15422_-142-15 others(16): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839351 | ||||||
chr5:88839351
|
C | CTCTCTCT others(1): Show |
13 | a0001c0001t0002g0186a0001c0001t0002g0191a0001c0001t0002g0193others(10): Show | 13 | HG01243.hp2 HG01361.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.-142-15422_-142-15 others(14): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839351 | ||||||
chr5:88839351
|
C | CTCTCTCT others(5): Show |
12 | a0001c0001t0003g0276a0001c0001t0004g0256a0001c0001t0004g0283others(9): Show | 12 | HG01496.hp1 HG02615.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.-142-15422_-142-15 others(18): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839351 | ||||||
chr5:88839351
|
C | CTCTCTCT others(3): Show |
11 | a0001c0001t0002g0187a0001c0001t0002g0188a0001c0001t0002g0189others(8): Show | 11 | HG02129.hp2 HG02148.hp2 HG02273.hp2 others(8): Show |
intron_variant | MODIFIER | c.-142-15422_-142-15 others(16): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839351 | ||||||
chr5:88839355
|
A | C | 1 | a0001c0001t0008g0035 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-142-15425T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839355 | ||||||
chr5:88839645
|
T | C | 168 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(165): Show | 168 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(165): Show |
intron_variant | MODIFIER | c.-142-15715A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839645 | ||||||
chr5:88839661
|
T | C | 2 | a0001c0001t0019g0067a0001c0001t0024g0066 | 2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-142-15731A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839661 | ||||||
chr5:88839670
|
G | A | 2 | a0001c0001t0028g0170a0001c0001t0031g0167 | 2 | HG02602.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.-142-15740C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839670 | ||||||
chr5:88839791
|
C | T | 2 | a0001c0001t0007g0017a0001c0001t0007g0018 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-142-15861G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839791 | ||||||
chr5:88839891
|
G | T | 1 | a0001c0001t0001g0180 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-142-15961C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839891 | ||||||
chr5:88839970
|
C | A | 1 | a0001c0001t0034g0012 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-142-16040G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88839970 | ||||||
chr5:88840599
|
C | T | 45 | a0001c0001t0002g0182a0001c0001t0002g0183a0001c0001t0002g0186others(42): Show | 45 | HG00597.hp1 HG01243.hp2 HG01361.hp1 others(42): Show |
intron_variant | MODIFIER | c.-142-16669G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88840599 | ||||||
chr5:88840862
|
G | C | 1 | a0001c0001t0004g0246 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-142-16932C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88840862 | ||||||
chr5:88840893
|
T | G | 1 | a0001c0001t0001g0061 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-142-16963A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88840893 | ||||||
chr5:88841429
|
C | T | 10 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0077others(7): Show | 10 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-142-17499G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88841429 | ||||||
chr5:88841506
|
CA | C | 146 | a0001c0001t0001g0065a0001c0001t0001g0090a0001c0001t0001g0110others(143): Show | 146 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(143): Show |
intron_variant | MODIFIER | c.-142-17577delT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88841506 | ||||||
chr5:88841506
|
CAA | C | 24 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(21): Show | 24 | HG00733.hp1 HG01081.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.-142-17578_-142-17 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88841506 | ||||||
chr5:88841527
|
GA | G | 74 | a0001c0001t0001g0267a0001c0001t0001g0273a0001c0001t0002g0023others(71): Show | 74 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(71): Show |
intron_variant | MODIFIER | c.-142-17598delT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88841527 | ||||||
chr5:88841633
|
A | C | 1 | a0001c0001t0001g0171 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-142-17703T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88841633 | ||||||
chr5:88841664
|
T | A | 74 | a0001c0001t0001g0267a0001c0001t0001g0273a0001c0001t0002g0023others(71): Show | 74 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(71): Show |
intron_variant | MODIFIER | c.-142-17734A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88841664 | ||||||
chr5:88841830
|
C | T | 10 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0077others(7): Show | 10 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-142-17900G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88841830 | ||||||
chr5:88842208
|
C | T | 1 | a0001c0001t0022g0211 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-142-18278G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88842208 | ||||||
chr5:88842225
|
G | A | 169 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(166): Show | 169 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(166): Show |
intron_variant | MODIFIER | c.-142-18295C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88842225 | ||||||
chr5:88842345
|
A | G | 2 | a0001c0001t0002g0026a0001c0001t0002g0027 | 2 | HG03834.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-142-18415T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88842345 | ||||||
chr5:88842529
|
G | A | 1 | a0001c0001t0019g0067 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-142-18599C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88842529 | ||||||
chr5:88842541
|
GA | G | 12 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0077others(9): Show | 12 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.-142-18612delT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88842541 | ||||||
chr5:88842594
|
C | CATTT | 169 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(166): Show | 169 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(166): Show |
intron_variant | MODIFIER | c.-142-18665_-142-18 others(10): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88842594 | ||||||
chr5:88842679
|
T | C | 2 | a0001c0001t0004g0108a0001c0001t0030g0109 | 2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-142-18749A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88842679 | ||||||
chr5:88842730
|
T | A | 34 | a0001c0001t0001g0267a0001c0001t0001g0273a0001c0001t0002g0268others(31): Show | 34 | HG01069.hp2 HG01070.hp2 HG01358.hp2 others(31): Show |
intron_variant | MODIFIER | c.-142-18800A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88842730 | ||||||
chr5:88842773
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-142-18843G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88842773 | ||||||
chr5:88842901
|
C | A | 10 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0077others(7): Show | 10 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-142-18971G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88842901 | ||||||
chr5:88842914
|
C | T | 7 | a0001c0001t0001g0110a0001c0001t0003g0113a0001c0001t0004g0011others(4): Show | 7 | HG00639.hp2 HG01192.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.-142-18984G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88842914 | ||||||
chr5:88842989
|
C | T | 1 | a0001c0001t0036g0015 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-142-19059G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88842989 | ||||||
chr5:88843209
|
C | CT | 120 | a0001c0001t0001g0001a0001c0001t0001g0024a0001c0001t0001g0029others(117): Show | 120 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.-142-19280dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88843209 | ||||||
chr5:88843251
|
C | T | 1 | a0001c0001t0003g0091 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-142-19321G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88843251 | ||||||
chr5:88843271
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-142-19341A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88843271 | ||||||
chr5:88843353
|
C | CA | 9 | a0001c0001t0001g0110a0001c0001t0003g0113a0001c0001t0003g0245others(6): Show | 9 | HG00639.hp2 HG01192.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.-142-19424dupT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88843353 | ||||||
chr5:88843805
|
C | CT | 6 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0075others(3): Show | 6 | HG01433.hp1 HG02145.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.-142-19876dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88843805 | ||||||
chr5:88843805
|
CT | C | 96 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0110others(93): Show | 96 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.-142-19876delA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88843805 | ||||||
chr5:88843892
|
C | T | 10 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0077others(7): Show | 10 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-142-19962G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88843892 | ||||||
chr5:88843897
|
C | T | 1 | a0001c0001t0004g0297 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-142-19967G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88843897 | ||||||
chr5:88843961
|
C | T | 1 | a0001c0001t0031g0167 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-142-20031G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88843961 | ||||||
chr5:88843966
|
C | T | 1 | a0001c0001t0002g0206 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-142-20036G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88843966 | ||||||
chr5:88844213
|
G | A | 7 | a0001c0001t0004g0082a0001c0001t0004g0086a0001c0001t0004g0087others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-142-20283C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88844213 | ||||||
chr5:88844292
|
C | T | 1 | a0001c0001t0001g0001 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-142-20362G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88844292 | ||||||
chr5:88844324
|
T | C | 1 | a0001c0001t0001g0039 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-142-20394A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88844324 | ||||||
chr5:88844574
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-142-20644T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88844574 | ||||||
chr5:88844746
|
C | A | 1 | a0001c0001t0001g0090 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-142-20816G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88844746 | ||||||
chr5:88845125
|
G | A | 158 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(155): Show | 158 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(155): Show |
intron_variant | MODIFIER | c.-142-21195C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88845125 | ||||||
chr5:88845145
|
T | C | 151 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(148): Show | 151 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(148): Show |
intron_variant | MODIFIER | c.-142-21215A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88845145 | ||||||
chr5:88845181
|
C | T | 7 | a0001c0001t0004g0082a0001c0001t0004g0086a0001c0001t0004g0087others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-142-21251G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88845181 | ||||||
chr5:88845213
|
G | T | 168 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(165): Show | 168 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(165): Show |
intron_variant | MODIFIER | c.-142-21283C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88845213 | ||||||
chr5:88845441
|
T | C | 1 | a0001c0001t0001g0273 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-142-21511A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88845441 | ||||||
chr5:88845473
|
G | A | 1 | a0001c0001t0003g0091 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-142-21543C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88845473 | ||||||
chr5:88845626
|
A | G | 1 | a0001c0001t0003g0010 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-142-21696T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88845626 | ||||||
chr5:88845655
|
G | A | 3 | a0001c0001t0002g0073a0001c0001t0016g0074a0001c0001t0016g0079 | 3 | HG01169.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-142-21725C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88845655 | ||||||
chr5:88845723
|
G | A | 10 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0077others(7): Show | 10 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-142-21793C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88845723 | ||||||
chr5:88845770
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG02257.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-142-21840C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88845770 | ||||||
chr5:88845772
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG02257.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-142-21842C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88845772 | ||||||
chr5:88845945
|
T | C | 1 | a0001c0001t0008g0107 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-142-22015A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88845945 | ||||||
chr5:88845984
|
T | G | 2 | a0001c0001t0001g0052a0001c0001t0003g0010 | 2 | HG02040.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-142-22054A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88845984 | ||||||
chr5:88846016
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-142-22086T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88846016 | ||||||
chr5:88846070
|
CT | C | 8 | a0001c0001t0001g0029a0001c0001t0001g0273a0001c0001t0003g0281others(5): Show | 8 | HG02132.hp1 NA18941.hp1 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.-142-22141delA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88846070 | ||||||
chr5:88846208
|
C | A | 1 | a0001c0001t0034g0012 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-142-22278G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88846208 | ||||||
chr5:88846230
|
G | A | 5 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0015g0081others(2): Show | 5 | HG00639.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-142-22300C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88846230 | ||||||
chr5:88846358
|
A | G | 1 | a0001c0001t0003g0185 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-142-22428T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88846358 | ||||||
chr5:88846619
|
G | C | 1 | a0001c0001t0003g0091 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-142-22689C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88846619 | ||||||
chr5:88847392
|
A | G | 1 | a0001c0001t0004g0098 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-142-23462T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88847392 | ||||||
chr5:88847709
|
C | T | 169 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(166): Show | 169 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(166): Show |
intron_variant | MODIFIER | c.-142-23779G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88847709 | ||||||
chr5:88847809
|
A | T | 15 | a0001c0001t0001g0065a0001c0001t0002g0021a0001c0001t0002g0030others(12): Show | 15 | HG01433.hp1 HG01515.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.-142-23879T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88847809 | ||||||
chr5:88847932
|
A | G | 54 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(51): Show | 54 | HG00597.hp1 HG01243.hp1 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.-142-24002T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88847932 | ||||||
chr5:88847979
|
C | T | 5 | a0001c0001t0003g0233a0001c0001t0003g0235a0001c0001t0003g0252others(2): Show | 5 | HG00642.hp1 HG01192.hp2 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.-142-24049G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88847979 | ||||||
chr5:88848209
|
A | G | 169 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(166): Show | 169 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(166): Show |
intron_variant | MODIFIER | c.-142-24279T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88848209 | ||||||
chr5:88848274
|
T | C | 77 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(74): Show | 77 | HG00597.hp1 HG00639.hp1 HG01243.hp1 others(74): Show |
intron_variant | MODIFIER | c.-142-24344A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88848274 | ||||||
chr5:88848417
|
G | A | 51 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(48): Show | 51 | HG00597.hp1 HG01243.hp2 HG01361.hp1 others(48): Show |
intron_variant | MODIFIER | c.-142-24487C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88848417 | ||||||
chr5:88848479
|
G | C | 2 | a0001c0001t0002g0191a0001c0001t0004g0002 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-142-24549C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88848479 | ||||||
chr5:88848703
|
A | G | 168 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(165): Show | 168 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(165): Show |
intron_variant | MODIFIER | c.-142-24773T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88848703 | ||||||
chr5:88848852
|
T | C | 74 | a0001c0001t0001g0267a0001c0001t0001g0273a0001c0001t0002g0023others(71): Show | 74 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(71): Show |
intron_variant | MODIFIER | c.-142-24922A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88848852 | ||||||
chr5:88848869
|
T | C | 73 | a0001c0001t0001g0267a0001c0001t0001g0273a0001c0001t0002g0232others(70): Show | 73 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.-142-24939A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88848869 | ||||||
chr5:88848877
|
G | T | 1 | a0001c0001t0002g0183 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-142-24947C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88848877 | ||||||
chr5:88849005
|
G | A | 2 | a0001c0001t0015g0081a0001c0001t0015g0089 | 2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-142-25075C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88849005 | ||||||
chr5:88849008
|
G | A | 1 | a0001c0001t0003g0248 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-142-25078C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88849008 | ||||||
chr5:88849083
|
A | G | 1 | a0001c0001t0002g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-142-25153T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88849083 | ||||||
chr5:88849145
|
T | G | 20 | a0001c0001t0002g0183a0001c0001t0002g0198a0001c0001t0002g0199others(17): Show | 20 | HG00597.hp1 HG04184.hp1 NA18944.hp1 others(17): Show |
intron_variant | MODIFIER | c.-142-25215A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88849145 | ||||||
chr5:88849150
|
C | CA | 34 | a0001c0001t0001g0040a0001c0001t0001g0058a0001c0001t0001g0072others(31): Show | 34 | HG00544.hp1 HG00597.hp1 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.-142-25221dupT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88849150 | ||||||
chr5:88849150
|
C | CAA | 64 | a0001c0001t0001g0267a0001c0001t0001g0273a0001c0001t0002g0232others(61): Show | 64 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.-142-25222_-142-25 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88849150 | ||||||
chr5:88849150
|
C | CAAA | 13 | a0001c0001t0001g0110a0001c0001t0003g0113a0001c0001t0003g0230others(10): Show | 13 | HG00639.hp2 HG01192.hp1 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.-142-25223_-142-25 others(9): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88849150 | ||||||
chr5:88849150
|
CA | C | 21 | a0001c0001t0001g0029a0001c0001t0001g0118a0001c0001t0001g0129others(18): Show | 21 | HG00639.hp1 HG01255.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.-142-25221delT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88849150 | ||||||
chr5:88849172
|
T | C | 10 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0077others(7): Show | 10 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-142-25242A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88849172 | ||||||
chr5:88849174
|
C | A | 1 | a0001c0001t0035g0085 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-142-25244G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88849174 | ||||||
chr5:88849267
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-142-25337G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88849267 | ||||||
chr5:88849306
|
A | G | 2 | a0001c0001t0001g0117a0001c0001t0002g0152 | 2 | NA18956.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-142-25376T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88849306 | ||||||
chr5:88849647
|
T | C | 1 | a0001c0001t0013g0145 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-142-25717A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88849647 | ||||||
chr5:88849653
|
G | A | 2 | a0001c0001t0004g0108a0001c0001t0030g0109 | 2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-142-25723C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88849653 | ||||||
chr5:88849661
|
A | G | 1 | a0001c0001t0002g0216 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-142-25731T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88849661 | ||||||
chr5:88850014
|
C | T | 1 | a0001c0001t0033g0060 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-142-26084G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88850014 | ||||||
chr5:88850084
|
C | G | 15 | a0001c0001t0001g0065a0001c0001t0002g0021a0001c0001t0002g0030others(12): Show | 15 | HG01433.hp1 HG01515.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.-142-26154G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88850084 | ||||||
chr5:88850105
|
G | GA | 88 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0092others(85): Show | 88 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.-142-26176_-142-26 others(7): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88850105 | ||||||
chr5:88850106
|
C | G | 88 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0092others(85): Show | 88 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.-142-26176G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88850106 | ||||||
chr5:88850125
|
C | T | 1 | a0001c0001t0004g0256 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-142-26195G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88850125 | ||||||
chr5:88850183
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-142-26253C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88850183 | ||||||
chr5:88850460
|
G | A | 1 | a0001c0001t0008g0107 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-142-26530C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88850460 | ||||||
chr5:88850503
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-142-26573T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88850503 | ||||||
chr5:88850688
|
A | G | 10 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0077others(7): Show | 10 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-142-26758T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88850688 | ||||||
chr5:88850721
|
T | C | 10 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0077others(7): Show | 10 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-142-26791A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88850721 | ||||||
chr5:88850883
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-142-26953C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88850883 | ||||||
chr5:88850956
|
T | G | 3 | a0001c0001t0005g0013a0001c0001t0005g0014a0001c0001t0036g0015 | 3 | HG01243.hp1 HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-142-27026A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88850956 | ||||||
chr5:88851035
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-142-27105A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88851035 | ||||||
chr5:88851102
|
G | A | 1 | a0001c0001t0034g0012 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-142-27172C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88851102 | ||||||
chr5:88851188
|
G | A | 1 | a0001c0001t0001g0129 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-142-27258C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88851188 | ||||||
chr5:88851233
|
C | CA | 42 | a0001c0001t0001g0022a0001c0001t0002g0020a0001c0001t0002g0034others(39): Show | 42 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.-142-27304dupT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88851233 | ||||||
chr5:88851233
|
C | CAA | 72 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0065others(69): Show | 72 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.-142-27305_-142-27 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88851233 | ||||||
chr5:88851233
|
C | CAAA | 13 | a0001c0001t0001g0008a0001c0001t0002g0003a0001c0001t0002g0007others(10): Show | 13 | HG00597.hp1 HG01243.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.-142-27306_-142-27 others(9): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88851233 | ||||||
chr5:88851233
|
CA | C | 6 | a0001c0001t0001g0029a0001c0001t0001g0090a0001c0001t0002g0046others(3): Show | 6 | HG01884.hp1 HG02735.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.-142-27304delT | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88851233 | ||||||
chr5:88851233
|
CAA | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0092others(78): Show | 81 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.-142-27305_-142-27 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88851233 | ||||||
chr5:88851268
|
T | G | 1 | a0001c0001t0001g0061 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-142-27338A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88851268 | ||||||
chr5:88851281
|
C | A | 2 | a0001c0001t0007g0017a0001c0001t0007g0018 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-142-27351G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88851281 | ||||||
chr5:88851375
|
T | C | 71 | a0001c0001t0001g0267a0001c0001t0001g0273a0001c0001t0002g0232others(68): Show | 71 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.-142-27445A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88851375 | ||||||
chr5:88851443
|
T | A | 7 | a0001c0001t0001g0110a0001c0001t0003g0113a0001c0001t0004g0011others(4): Show | 7 | HG00639.hp2 HG01192.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.-142-27513A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88851443 | ||||||
chr5:88851565
|
A | T | 1 | a0001c0001t0001g0101 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-142-27635T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88851565 | ||||||
chr5:88851643
|
C | T | 1 | a0001c0001t0002g0198 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-142-27713G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88851643 | ||||||
chr5:88851816
|
A | C | 1 | a0001c0001t0008g0068 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-142-27886T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88851816 | ||||||
chr5:88851954
|
G | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0090others(91): Show | 94 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.-142-28024C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88851954 | ||||||
chr5:88852072
|
A | G | 7 | a0001c0001t0001g0110a0001c0001t0003g0113a0001c0001t0004g0011others(4): Show | 7 | HG00639.hp2 HG01192.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.-142-28142T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88852072 | ||||||
chr5:88852122
|
C | T | 7 | a0001c0001t0001g0110a0001c0001t0003g0113a0001c0001t0004g0011others(4): Show | 7 | HG00639.hp2 HG01192.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.-142-28192G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88852122 | ||||||
chr5:88852224
|
C | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0090others(91): Show | 94 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.-142-28294G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88852224 | ||||||
chr5:88852233
|
T | C | 1 | a0001c0001t0003g0091 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-142-28303A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88852233 | ||||||
chr5:88852620
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-142-28690G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88852620 | ||||||
chr5:88852698
|
C | T | 1 | a0001c0001t0004g0256 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-142-28768G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88852698 | ||||||
chr5:88852700
|
G | A | 7 | a0001c0001t0001g0110a0001c0001t0003g0113a0001c0001t0004g0011others(4): Show | 7 | HG00639.hp2 HG01192.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.-142-28770C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88852700 | ||||||
chr5:88852821
|
A | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0090others(91): Show | 94 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.-142-28891T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88852821 | ||||||
chr5:88852826
|
A | C | 1 | a0001c0001t0025g0153 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-142-28896T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88852826 | ||||||
chr5:88852872
|
G | A | 3 | a0001c0001t0005g0013a0001c0001t0005g0014a0001c0001t0036g0015 | 3 | HG01243.hp1 HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-142-28942C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88852872 | ||||||
chr5:88852879
|
C | T | 9 | a0001c0001t0001g0065a0001c0001t0005g0013a0001c0001t0005g0014others(6): Show | 9 | HG01243.hp1 HG01433.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.-142-28949G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88852879 | ||||||
chr5:88852884
|
C | T | 1 | a0001c0001t0012g0057 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-142-28954G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88852884 | ||||||
chr5:88852893
|
G | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0090others(91): Show | 94 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.-142-28963C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88852893 | ||||||
chr5:88853002
|
T | C | 1 | a0001c0001t0002g0217 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-142-29072A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88853002 | ||||||
chr5:88853041
|
T | C | 1 | a0001c0001t0003g0091 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-142-29111A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88853041 | ||||||
chr5:88853106
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-142-29176G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88853106 | ||||||
chr5:88853182
|
C | T | 2 | a0001c0001t0004g0086a0001c0001t0004g0087 | 2 | HG01884.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.-142-29252G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88853182 | ||||||
chr5:88853474
|
A | G | 94 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0090others(91): Show | 94 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.-143+29481T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88853474 | ||||||
chr5:88853509
|
G | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0090others(91): Show | 94 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.-143+29446C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88853509 | ||||||
chr5:88853592
|
A | T | 1 | a0001c0001t0002g0182 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-143+29363T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88853592 | ||||||
chr5:88853643
|
T | C | 6 | a0001c0001t0001g0065a0001c0001t0008g0068a0001c0001t0008g0069others(3): Show | 6 | HG01433.hp1 HG01515.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.-143+29312A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88853643 | ||||||
chr5:88853724
|
G | T | 4 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0015g0081others(1): Show | 4 | HG02572.hp1 HG03098.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-143+29231C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88853724 | ||||||
chr5:88853831
|
C | T | 4 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(1): Show | 4 | HG01168.hp2 HG01169.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.-143+29124G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88853831 | ||||||
chr5:88853836
|
G | T | 2 | a0001c0001t0002g0224a0001c0001t0002g0225 | 2 | NA18944.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.-143+29119C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88853836 | ||||||
chr5:88853930
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-143+29025G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88853930 | ||||||
chr5:88853955
|
T | C | 1 | a0001c0001t0020g0004 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-143+29000A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88853955 | ||||||
chr5:88854129
|
A | G | 38 | a0001c0001t0001g0267a0001c0001t0001g0273a0001c0001t0002g0268others(35): Show | 38 | HG01069.hp2 HG01070.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.-143+28826T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88854129 | ||||||
chr5:88854358
|
G | A | 2 | a0001c0001t0004g0108a0001c0001t0030g0109 | 2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-143+28597C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88854358 | ||||||
chr5:88854472
|
G | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0090others(91): Show | 94 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.-143+28483C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88854472 | ||||||
chr5:88854567
|
G | C | 10 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0077others(7): Show | 10 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-143+28388C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88854567 | ||||||
chr5:88854580
|
T | C | 2 | a0001c0001t0005g0013a0001c0001t0005g0014 | 2 | HG01243.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-143+28375A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88854580 | ||||||
chr5:88854606
|
T | C | 1 | a0001c0001t0002g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-143+28349A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88854606 | ||||||
chr5:88854650
|
T | C | 1 | a0001c0001t0002g0191 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-143+28305A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88854650 | ||||||
chr5:88854683
|
C | A | 1 | a0001c0001t0002g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-143+28272G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88854683 | ||||||
chr5:88854924
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-143+28031G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88854924 | ||||||
chr5:88854984
|
T | G | 10 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0077others(7): Show | 10 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-143+27971A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88854984 | ||||||
chr5:88855175
|
T | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0090others(91): Show | 94 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.-143+27780A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88855175 | ||||||
chr5:88855546
|
C | G | 1 | a0001c0001t0003g0250 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-143+27409G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88855546 | ||||||
chr5:88855610
|
C | A | 7 | a0001c0001t0004g0082a0001c0001t0004g0086a0001c0001t0004g0087others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-143+27345G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88855610 | ||||||
chr5:88855817
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-143+27138A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88855817 | ||||||
chr5:88855853
|
A | G | 1 | a0001c0001t0012g0138 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-143+27102T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88855853 | ||||||
chr5:88855856
|
G | A | 5 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0015g0081others(2): Show | 5 | HG00639.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-143+27099C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88855856 | ||||||
chr5:88855856
|
G | T | 1 | a0001c0001t0003g0249 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-143+27099C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88855856 | ||||||
chr5:88855971
|
C | A | 1 | a0001c0001t0002g0045 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-143+26984G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88855971 | ||||||
chr5:88856067
|
G | C | 3 | a0001c0001t0004g0082a0001c0001t0005g0083a0001c0001t0005g0084 | 3 | HG02451.hp1 HG02970.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-143+26888C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88856067 | ||||||
chr5:88856300
|
C | T | 252 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(249): Show | 252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.-143+26655G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88856300 | ||||||
chr5:88856385
|
T | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0090others(91): Show | 94 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.-143+26570A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88856385 | ||||||
chr5:88856521
|
G | A | 1 | a0001c0001t0020g0004 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-143+26434C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88856521 | ||||||
chr5:88856712
|
C | T | 45 | a0001c0001t0002g0182a0001c0001t0002g0183a0001c0001t0002g0186others(42): Show | 45 | HG00597.hp1 HG01243.hp2 HG01361.hp1 others(42): Show |
intron_variant | MODIFIER | c.-143+26243G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88856712 | ||||||
chr5:88856757
|
C | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0090others(91): Show | 94 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.-143+26198G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88856757 | ||||||
chr5:88857002
|
C | T | 2 | a0001c0001t0002g0026a0001c0001t0002g0027 | 2 | HG03834.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-143+25953G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88857002 | ||||||
chr5:88857152
|
T | C | 4 | a0001c0001t0004g0086a0001c0001t0004g0087a0001c0001t0004g0088others(1): Show | 4 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.-143+25803A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88857152 | ||||||
chr5:88857301
|
A | G | 1 | a0001c0001t0002g0050 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-143+25654T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88857301 | ||||||
chr5:88857579
|
C | T | 1 | a0001c0001t0002g0216 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-143+25376G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88857579 | ||||||
chr5:88857631
|
C | A | 6 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(3): Show | 6 | HG02257.hp2 HG02486.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-143+25324G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88857631 | ||||||
chr5:88857635
|
G | A | 5 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0015g0081others(2): Show | 5 | HG00639.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-143+25320C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88857635 | ||||||
chr5:88857872
|
C | T | 1 | a0001c0001t0002g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-143+25083G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88857872 | ||||||
chr5:88858024
|
C | T | 1 | a0001c0001t0007g0301 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-143+24931G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88858024 | ||||||
chr5:88858057
|
C | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0090others(91): Show | 94 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.-143+24898G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88858057 | ||||||
chr5:88858258
|
T | A | 7 | a0001c0001t0001g0110a0001c0001t0003g0113a0001c0001t0004g0011others(4): Show | 7 | HG00639.hp2 HG01192.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.-143+24697A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88858258 | ||||||
chr5:88858434
|
T | C | 1 | a0001c0001t0002g0234 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-143+24521A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88858434 | ||||||
chr5:88858542
|
G | A | 3 | a0001c0001t0005g0013a0001c0001t0005g0014a0001c0001t0036g0015 | 3 | HG01243.hp1 HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-143+24413C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88858542 | ||||||
chr5:88858798
|
T | A | 1 | a0001c0001t0034g0012 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-143+24157A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88858798 | ||||||
chr5:88858799
|
A | T | 45 | a0001c0001t0002g0182a0001c0001t0002g0183a0001c0001t0002g0186others(42): Show | 45 | HG00597.hp1 HG01243.hp2 HG01361.hp1 others(42): Show |
intron_variant | MODIFIER | c.-143+24156T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88858799 | ||||||
chr5:88858920
|
T | C | 3 | a0001c0001t0004g0082a0001c0001t0005g0083a0001c0001t0005g0084 | 3 | HG02451.hp1 HG02970.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-143+24035A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88858920 | ||||||
chr5:88858953
|
T | C | 1 | a0001c0001t0002g0049 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-143+24002A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88858953 | ||||||
chr5:88858981
|
C | T | 1 | a0001c0001t0015g0089 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-143+23974G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88858981 | ||||||
chr5:88859292
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-143+23663C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88859292 | ||||||
chr5:88859700
|
T | C | 7 | a0001c0001t0004g0082a0001c0001t0004g0086a0001c0001t0004g0087others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-143+23255A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88859700 | ||||||
chr5:88859705
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-143+23250C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88859705 | ||||||
chr5:88859775
|
T | C | 1 | a0001c0001t0002g0050 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-143+23180A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88859775 | ||||||
chr5:88860293
|
G | C | 2 | a0001c0001t0002g0042a0001c0001t0002g0043 | 2 | NA18747.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.-143+22662C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88860293 | ||||||
chr5:88860309
|
A | C | 1 | a0001c0001t0033g0060 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-143+22646T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88860309 | ||||||
chr5:88860323
|
C | CT | 10 | a0001c0001t0001g0072a0001c0001t0001g0077a0001c0001t0001g0078others(7): Show | 10 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-143+22631dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88860323 | ||||||
chr5:88860613
|
C | T | 1 | a0001c0001t0037g0236 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-143+22342G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88860613 | ||||||
chr5:88860637
|
G | A | 11 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0038others(8): Show | 11 | HG00544.hp1 HG02015.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.-143+22318C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88860637 | ||||||
chr5:88860749
|
T | C | 1 | a0001c0001t0028g0170 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-143+22206A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88860749 | ||||||
chr5:88860800
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-143+22155A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88860800 | ||||||
chr5:88860833
|
T | C | 1 | a0001c0001t0003g0249 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-143+22122A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88860833 | ||||||
chr5:88860897
|
T | C | 3 | a0001c0001t0001g0008a0001c0001t0002g0003a0001c0001t0002g0007 | 3 | HG02486.hp2 HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-143+22058A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88860897 | ||||||
chr5:88861006
|
C | T | 2 | a0001c0001t0015g0081a0001c0001t0015g0089 | 2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-143+21949G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88861006 | ||||||
chr5:88861153
|
C | T | 287 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.-143+21802G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88861153 | ||||||
chr5:88861164
|
C | T | 1 | a0001c0001t0002g0034 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-143+21791G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88861164 | ||||||
chr5:88861467
|
T | C | 1 | a0001c0001t0034g0012 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-143+21488A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88861467 | ||||||
chr5:88861484
|
G | A | 2 | a0001c0001t0015g0081a0001c0001t0015g0089 | 2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-143+21471C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88861484 | ||||||
chr5:88861735
|
T | C | 104 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0072others(101): Show | 104 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.-143+21220A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88861735 | ||||||
chr5:88861846
|
A | G | 2 | a0001c0001t0002g0224a0001c0001t0002g0225 | 2 | NA18944.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.-143+21109T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88861846 | ||||||
chr5:88861921
|
A | G | 1 | a0001c0001t0004g0164 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-143+21034T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88861921 | ||||||
chr5:88862065
|
T | C | 2 | a0001c0001t0002g0026a0001c0001t0002g0027 | 2 | HG03834.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-143+20890A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88862065 | ||||||
chr5:88862262
|
T | C | 5 | a0001c0001t0006g0133a0001c0001t0006g0134a0001c0001t0006g0148others(2): Show | 5 | NA18941.hp1 NA18945.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-143+20693A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88862262 | ||||||
chr5:88862329
|
G | C | 87 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0090others(84): Show | 87 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.-143+20626C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88862329 | ||||||
chr5:88862650
|
T | C | 1 | a0001c0001t0003g0091 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-143+20305A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88862650 | ||||||
chr5:88862669
|
AT | A | 12 | a0001c0001t0002g0183a0001c0001t0002g0198a0001c0001t0002g0199others(9): Show | 12 | HG00597.hp1 HG04184.hp1 NA18951.hp2 others(9): Show |
intron_variant | MODIFIER | c.-143+20285delA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88862669 | ||||||
chr5:88862847
|
G | A | 2 | a0001c0001t0003g0261a0001c0001t0003g0292 | 2 | HG01069.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.-143+20108C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88862847 | ||||||
chr5:88863274
|
T | C | 1 | a0001c0001t0002g0174 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-143+19681A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88863274 | ||||||
chr5:88863356
|
T | A | 250 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(247): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.-143+19599A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88863356 | ||||||
chr5:88863468
|
C | T | 4 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0015g0081others(1): Show | 4 | HG02572.hp1 HG03098.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-143+19487G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88863468 | ||||||
chr5:88863474
|
G | A | 10 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0077others(7): Show | 10 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-143+19481C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88863474 | ||||||
chr5:88863509
|
A | G | 1 | a0001c0001t0003g0252 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-143+19446T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88863509 | ||||||
chr5:88863706
|
T | C | 1 | a0001c0001t0003g0051 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-143+19249A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88863706 | ||||||
chr5:88863824
|
C | CT | 95 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0090others(92): Show | 95 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.-143+19130dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88863824 | ||||||
chr5:88863856
|
C | T | 1 | a0001c0001t0003g0294 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-143+19099G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88863856 | ||||||
chr5:88863891
|
G | A | 3 | a0001c0001t0002g0023a0001c0001t0007g0017a0001c0001t0007g0018 | 3 | HG02896.hp1 HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-143+19064C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88863891 | ||||||
chr5:88864023
|
T | C | 2 | a0001c0001t0004g0071a0001c0001t0004g0080 | 2 | HG00733.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.-143+18932A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88864023 | ||||||
chr5:88864149
|
T | G | 92 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0090others(89): Show | 92 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.-143+18806A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88864149 | ||||||
chr5:88864150
|
TG | T | 92 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0090others(89): Show | 92 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.-143+18804delC | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88864150 | ||||||
chr5:88864151
|
G | T | 1 | a0001c0001t0007g0301 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-143+18804C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88864151 | ||||||
chr5:88864151
|
GT | G | 157 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(154): Show | 157 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(154): Show |
intron_variant | MODIFIER | c.-143+18803delA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88864151 | ||||||
chr5:88864152
|
T | G | 1 | a0001c0001t0007g0301 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-143+18803A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88864152 | ||||||
chr5:88864381
|
A | C | 7 | a0001c0001t0001g0110a0001c0001t0003g0113a0001c0001t0004g0011others(4): Show | 7 | HG00639.hp2 HG01192.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.-143+18574T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88864381 | ||||||
chr5:88864537
|
C | T | 102 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0072others(99): Show | 102 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.-143+18418G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88864537 | ||||||
chr5:88864643
|
G | A | 10 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0077others(7): Show | 10 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-143+18312C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88864643 | ||||||
chr5:88864725
|
G | C | 5 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0015g0081others(2): Show | 5 | HG00639.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-143+18230C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88864725 | ||||||
chr5:88864767
|
A | T | 3 | a0001c0001t0001g0141a0001c0001t0002g0102a0001c0001t0002g0132 | 3 | NA19065.hp1 NA19065.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-143+18188T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88864767 | ||||||
chr5:88864767
|
AT | A | 73 | a0001c0001t0001g0122a0001c0001t0001g0273a0001c0001t0002g0189others(70): Show | 73 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.-143+18187delA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88864767 | ||||||
chr5:88864836
|
G | A | 3 | a0001c0001t0005g0013a0001c0001t0019g0067a0001c0001t0024g0066 | 3 | HG01243.hp1 HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-143+18119C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88864836 | ||||||
chr5:88864846
|
C | T | 10 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0077others(7): Show | 10 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-143+18109G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88864846 | ||||||
chr5:88864895
|
G | A | 2 | a0001c0001t0001g0117a0001c0001t0002g0152 | 2 | NA18956.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-143+18060C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88864895 | ||||||
chr5:88864905
|
T | C | 1 | a0001c0001t0034g0012 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-143+18050A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88864905 | ||||||
chr5:88864998
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-143+17957G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88864998 | ||||||
chr5:88865020
|
C | T | 3 | a0001c0001t0004g0082a0001c0001t0005g0083a0001c0001t0005g0084 | 3 | HG02451.hp1 HG02970.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-143+17935G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88865020 | ||||||
chr5:88865493
|
T | C | 1 | a0001c0001t0002g0280 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-143+17462A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88865493 | ||||||
chr5:88865564
|
G | T | 1 | a0001c0001t0007g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-143+17391C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88865564 | ||||||
chr5:88865600
|
T | C | 102 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0072others(99): Show | 102 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.-143+17355A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88865600 | ||||||
chr5:88865834
|
G | T | 7 | a0001c0001t0007g0017a0001c0001t0007g0018a0001c0001t0007g0300others(4): Show | 7 | HG00639.hp1 HG02572.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-143+17121C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88865834 | ||||||
chr5:88865853
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-143+17102A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88865853 | ||||||
chr5:88865893
|
T | C | 4 | a0001c0001t0007g0300a0001c0001t0007g0301a0001c0001t0015g0081others(1): Show | 4 | HG02572.hp1 HG03098.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-143+17062A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88865893 | ||||||
chr5:88865899
|
T | C | 1 | a0001c0001t0002g0043 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-143+17056A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88865899 | ||||||
chr5:88865947
|
G | C | 1 | a0001c0001t0003g0025 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-143+17008C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88865947 | ||||||
chr5:88865967
|
C | T | 1 | a0001c0001t0003g0250 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-143+16988G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88865967 | ||||||
chr5:88866032
|
G | T | 9 | a0001c0001t0001g0065a0001c0001t0005g0013a0001c0001t0005g0014others(6): Show | 9 | HG01243.hp1 HG01433.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.-143+16923C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88866032 | ||||||
chr5:88866057
|
G | A | 1 | a0001c0001t0034g0012 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-143+16898C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88866057 | ||||||
chr5:88866165
|
G | A | 9 | a0001c0001t0001g0065a0001c0001t0005g0013a0001c0001t0005g0014others(6): Show | 9 | HG01243.hp1 HG01433.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.-143+16790C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88866165 | ||||||
chr5:88866221
|
T | A | 10 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0077others(7): Show | 10 | HG00733.hp1 HG01081.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-143+16734A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88866221 | ||||||
chr5:88866277
|
A | C | 1 | a0001c0001t0001g0139 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-143+16678T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88866277 | ||||||
chr5:88866331
|
G | A | 1 | a0001c0001t0002g0132 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-143+16624C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88866331 | ||||||
chr5:88866428
|
C | G | 7 | a0001c0001t0001g0110a0001c0001t0003g0113a0001c0001t0004g0011others(4): Show | 7 | HG00639.hp2 HG01192.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.-143+16527G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88866428 | ||||||
chr5:88866485
|
G | A | 2 | a0001c0001t0001g0090a0001c0001t0003g0091 | 2 | HG01884.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-143+16470C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88866485 | ||||||
chr5:88866593
|
G | A | 1 | a0001c0001t0003g0294 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-143+16362C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88866593 | ||||||
chr5:88866859
|
T | C | 2 | a0001c0001t0003g0238a0001c0001t0003g0266 | 2 | HG01099.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.-143+16096A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88866859 | ||||||
chr5:88866940
|
G | C | 13 | a0001c0001t0002g0183a0001c0001t0002g0198a0001c0001t0002g0199others(10): Show | 13 | HG00597.hp1 HG04184.hp1 NA18951.hp2 others(10): Show |
intron_variant | MODIFIER | c.-143+16015C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88866940 | ||||||
chr5:88867032
|
C | T | 1 | a0001c0001t0001g0124 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-143+15923G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88867032 | ||||||
chr5:88867117
|
T | A | 8 | a0001c0001t0001g0029a0001c0001t0002g0021a0001c0001t0002g0030others(5): Show | 8 | HG02027.hp1 NA18747.hp1 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.-143+15838A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88867117 | ||||||
chr5:88867520
|
A | C | 1 | a0001c0001t0012g0138 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-143+15435T>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88867520 | ||||||
chr5:88867917
|
C | T | 2 | a0001c0001t0003g0230a0001c0001t0003g0231 | 2 | HG02486.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-143+15038G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88867917 | ||||||
chr5:88867919
|
C | T | 1 | a0001c0001t0002g0192 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-143+15036G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88867919 | ||||||
chr5:88867954
|
G | A | 106 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0072others(103): Show | 106 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.-143+15001C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88867954 | ||||||
chr5:88868251
|
AT | A | 7 | a0001c0001t0001g0110a0001c0001t0003g0113a0001c0001t0004g0011others(4): Show | 7 | HG00639.hp2 HG01192.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.-143+14703delA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88868251 | ||||||
chr5:88868260
|
T | A | 2 | a0001c0001t0001g0090a0001c0001t0003g0091 | 2 | HG01884.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-143+14695A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88868260 | ||||||
chr5:88868314
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-143+14641T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88868314 | ||||||
chr5:88868370
|
C | A | 9 | a0001c0001t0001g0065a0001c0001t0005g0013a0001c0001t0005g0014others(6): Show | 9 | HG01243.hp1 HG01433.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.-143+14585G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88868370 | ||||||
chr5:88868412
|
G | A | 1 | a0001c0001t0003g0255 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-143+14543C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88868412 | ||||||
chr5:88868677
|
T | A | 1 | a0001c0001t0004g0256 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-143+14278A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88868677 | ||||||
chr5:88868782
|
G | A | 1 | a0001c0001t0001g0005 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-143+14173C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88868782 | ||||||
chr5:88868906
|
C | T | 1 | a0001c0001t0007g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-143+14049G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88868906 | ||||||
chr5:88869189
|
A | G | 1 | a0001c0001t0001g0024 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-143+13766T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869189 | ||||||
chr5:88869252
|
C | CAT | 3 | a0001c0001t0001g0137a0001c0001t0001g0161a0001c0001t0001g0163 | 3 | HG00642.hp2 HG01255.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-143+13701_-143+13 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869252 | ||||||
chr5:88869252
|
C | CATATATA others(3): Show |
1 | a0001c0001t0010g0056 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-143+13693_-143+13 others(16): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869252 | ||||||
chr5:88869252
|
C | CATATATA others(9): Show |
1 | a0001c0001t0003g0258 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-143+13687_-143+13 others(22): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869252 | ||||||
chr5:88869252
|
CAT | C | 27 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(24): Show | 27 | HG00099.hp1 HG00733.hp2 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.-143+13701_-143+13 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869252 | ||||||
chr5:88869252
|
CATATATA others(23): Show |
C | 1 | a0001c0001t0003g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-143+13673_-143+13 others(36): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869252 | ||||||
chr5:88869254
|
T | TATATATA others(49): Show |
1 | a0001c0001t0002g0210 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-143+13700_-143+13 others(62): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869254 | ||||||
chr5:88869254
|
T | TATATATA others(69): Show |
1 | a0001c0001t0022g0211 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-143+13700_-143+13 others(82): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869254 | ||||||
chr5:88869254
|
T | TATATATA others(33): Show |
1 | a0001c0001t0001g0061 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-143+13700_-143+13 others(46): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869254 | ||||||
chr5:88869256
|
T | TATATATA others(47): Show |
4 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0221others(1): Show | 4 | NA18949.hp2 NA18965.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.-143+13698_-143+13 others(60): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869256 | ||||||
chr5:88869258
|
T | TATATATA others(69): Show |
2 | a0001c0001t0002g0189a0001c0001t0002g0212 | 2 | NA18999.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.-143+13696_-143+13 others(82): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869258 | ||||||
chr5:88869260
|
T | TATATATA others(29): Show |
1 | a0001c0001t0001g0101 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-143+13694_-143+13 others(42): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869260 | ||||||
chr5:88869260
|
TATATATA others(11): Show |
T | 8 | a0001c0001t0001g0110a0001c0001t0003g0091a0001c0001t0003g0113others(5): Show | 8 | HG00639.hp2 HG01192.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.-143+13677_-143+13 others(24): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869260 | ||||||
chr5:88869262
|
TATATATA others(9): Show |
T | 1 | a0001c0001t0034g0012 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-143+13677_-143+13 others(22): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869262 | ||||||
chr5:88869264
|
T | C | 1 | a0001c0001t0003g0282 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-143+13691A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869264 | ||||||
chr5:88869264
|
TATATATA others(7): Show |
T | 4 | a0001c0001t0001g0090a0001c0001t0002g0207a0001c0001t0004g0208others(1): Show | 4 | HG01884.hp1 HG02055.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-143+13677_-143+13 others(20): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869264 | ||||||
chr5:88869266
|
TATATATA others(5): Show |
T | 26 | a0001c0001t0001g0052a0001c0001t0002g0182a0001c0001t0002g0183others(23): Show | 26 | HG00597.hp1 HG01168.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.-143+13677_-143+13 others(18): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869266 | ||||||
chr5:88869267
|
A | G | 1 | a0001c0001t0003g0259 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-143+13688T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869267 | ||||||
chr5:88869268
|
TATATATA others(3): Show |
T | 22 | a0001c0001t0001g0065a0001c0001t0001g0116a0001c0001t0002g0020others(19): Show | 22 | HG01123.hp1 HG01496.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.-143+13677_-143+13 others(16): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869268 | ||||||
chr5:88869270
|
TATATATA others(1): Show |
T | 18 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0039others(15): Show | 18 | HG00544.hp1 HG01891.hp2 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.-143+13677_-143+13 others(14): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869270 | ||||||
chr5:88869272
|
T | TATATATA others(53): Show |
1 | a0001c0001t0023g0209 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-143+13682_-143+13 others(66): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869272 | ||||||
chr5:88869272
|
T | TATATATA others(35): Show |
1 | a0001c0001t0011g0055 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-143+13682_-143+13 others(48): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869272 | ||||||
chr5:88869272
|
TATATAC | T | 19 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0031others(16): Show | 19 | HG00642.hp1 HG01099.hp1 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.-143+13677_-143+13 others(12): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869272 | ||||||
chr5:88869274
|
TATAC | T | 28 | a0001c0001t0001g0029a0001c0001t0001g0092a0001c0001t0001g0106others(25): Show | 28 | HG01358.hp2 HG01891.hp1 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.-143+13677_-143+13 others(10): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869274 | ||||||
chr5:88869274
|
TATACATA others(15): Show |
T | 3 | a0001c0001t0002g0023a0001c0001t0007g0017a0001c0001t0007g0018 | 3 | HG02896.hp1 HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-143+13659_-143+13 others(28): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869274 | ||||||
chr5:88869275
|
A | ATATATAC others(77): Show |
1 | a0001c0001t0002g0216 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-143+13679_-143+13 others(90): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869275 | ||||||
chr5:88869276
|
T | C | 3 | a0001c0001t0001g0001a0001c0001t0004g0098a0001c0001t0009g0175 | 3 | HG01358.hp1 HG01928.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-143+13679A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869276 | ||||||
chr5:88869276
|
TAC | T | 34 | a0001c0001t0001g0008a0001c0001t0001g0063a0001c0001t0001g0267others(31): Show | 34 | HG00099.hp2 HG00673.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.-143+13677_-143+13 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869276 | ||||||
chr5:88869276
|
TACATATA others(13): Show |
T | 1 | a0001c0001t0004g0239 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-143+13659_-143+13 others(26): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869276 | ||||||
chr5:88869277
|
A | ATATATAC others(101): Show |
1 | a0001c0001t0001g0190 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-143+13677_-143+13 others(114): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869277 | ||||||
chr5:88869278
|
C | T | 38 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0022others(35): Show | 38 | HG00741.hp1 HG01069.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.-143+13677G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869278 | ||||||
chr5:88869280
|
T | C | 16 | a0001c0001t0001g0092a0001c0001t0001g0106a0001c0001t0001g0129others(13): Show | 16 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-143+13675A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869280 | ||||||
chr5:88869280
|
T | TATATACA others(49): Show |
1 | a0001c0001t0002g0213 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-143+13674_-143+13 others(62): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869280 | ||||||
chr5:88869280
|
T | TATATACA others(63): Show |
1 | a0001c0001t0002g0214 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-143+13674_-143+13 others(76): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869280 | ||||||
chr5:88869280
|
T | TATATATA others(29): Show |
3 | a0001c0001t0001g0161a0001c0001t0002g0162a0001c0001t0018g0119 | 3 | HG01123.hp2 HG01255.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.-143+13639_-143+13 others(42): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869280 | ||||||
chr5:88869280
|
T | TATATATA others(11): Show |
1 | a0001c0001t0001g0072 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-143+13674_-143+13 others(24): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869280 | ||||||
chr5:88869280
|
T | TATATATA others(15): Show |
2 | a0001c0001t0001g0077a0001c0001t0001g0078 | 2 | HG02809.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-143+13674_-143+13 others(28): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869280 | ||||||
chr5:88869281
|
A | G | 1 | a0001c0001t0034g0012 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-143+13674T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869281 | ||||||
chr5:88869284
|
T | C | 3 | a0001c0001t0002g0187a0001c0001t0002g0188a0001c0001t0002g0220 | 3 | HG02148.hp2 HG02273.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-143+13671A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869284 | ||||||
chr5:88869286
|
T | C | 1 | a0001c0001t0002g0226 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-143+13669A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869286 | ||||||
chr5:88869294
|
T | C | 3 | a0001c0001t0001g0097a0001c0001t0004g0098a0001c0001t0009g0175 | 3 | HG01928.hp1 HG02965.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.-143+13661A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869294 | ||||||
chr5:88869296
|
C | T | 45 | a0001c0001t0001g0022a0001c0001t0001g0061a0001c0001t0001g0110others(42): Show | 45 | HG00639.hp1 HG00639.hp2 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.-143+13659G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869296 | ||||||
chr5:88869296
|
CACAT | C | 55 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(52): Show | 55 | HG00544.hp1 HG01123.hp1 HG01433.hp1 others(52): Show |
intron_variant | MODIFIER | c.-143+13655_-143+13 others(10): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869296 | ||||||
chr5:88869296
|
CACATAT | C | 92 | a0001c0001t0001g0090a0001c0001t0001g0267a0001c0001t0001g0273others(89): Show | 92 | HG00099.hp2 HG00597.hp1 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.-143+13653_-143+13 others(12): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869296 | ||||||
chr5:88869298
|
C | T | 30 | a0001c0001t0001g0097a0001c0001t0001g0190a0001c0001t0002g0003others(27): Show | 30 | HG01243.hp1 HG01928.hp1 HG02129.hp2 others(27): Show |
intron_variant | MODIFIER | c.-143+13657G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869298 | ||||||
chr5:88869300
|
T | C | 4 | a0001c0001t0002g0003a0001c0001t0002g0174a0001c0001t0005g0013others(1): Show | 4 | HG01069.hp1 HG01243.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-143+13655A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869300 | ||||||
chr5:88869300
|
T | TATATATA others(27): Show |
2 | a0001c0001t0001g0163a0001c0001t0001g0173 | 2 | HG01515.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.-143+13654_-143+13 others(40): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869300 | ||||||
chr5:88869300
|
T | TATATATA others(27): Show |
1 | a0001c0001t0004g0164 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-143+13654_-143+13 others(40): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869300 | ||||||
chr5:88869300
|
T | TATATATA others(29): Show |
1 | a0001c0001t0001g0123 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-143+13654_-143+13 others(42): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869300 | ||||||
chr5:88869302
|
T | C | 12 | a0001c0001t0002g0189a0001c0001t0002g0210a0001c0001t0002g0212others(9): Show | 12 | HG02129.hp2 HG03139.hp2 HG03209.hp1 others(9): Show |
intron_variant | MODIFIER | c.-143+13653A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869302 | ||||||
chr5:88869302
|
T | TATATACA others(57): Show |
1 | a0001c0001t0002g0206 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-143+13652_-143+13 others(70): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869302 | ||||||
chr5:88869303
|
A | ACG | 4 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0221others(1): Show | 4 | NA18949.hp2 NA18965.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.-143+13651_-143+13 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869303 | ||||||
chr5:88869303
|
A | ATATACAT others(47): Show |
1 | a0001c0001t0002g0188 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-143+13651_-143+13 others(60): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869303 | ||||||
chr5:88869303
|
A | ATATACGT others(47): Show |
1 | a0001c0001t0002g0187 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-143+13651_-143+13 others(60): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869303 | ||||||
chr5:88869303
|
A | ATATATAC others(49): Show |
2 | a0001c0001t0002g0220a0001c0001t0002g0226 | 2 | HG02132.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-143+13651_-143+13 others(62): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869303 | ||||||
chr5:88869303
|
A | G | 1 | a0001c0001t0002g0189 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-143+13652T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869303 | ||||||
chr5:88869312
|
TATAC | T | 4 | a0001c0001t0003g0255a0001c0001t0003g0261a0001c0001t0003g0292others(1): Show | 4 | HG00741.hp1 HG01069.hp2 HG01070.hp2 others(1): Show |
intron_variant | MODIFIER | c.-143+13639_-143+13 others(10): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869312 | ||||||
chr5:88869314
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-143+13641A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869314 | ||||||
chr5:88869314
|
TAC | T | 11 | a0001c0001t0001g0022a0001c0001t0001g0061a0001c0001t0002g0023others(8): Show | 11 | HG02451.hp1 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.-143+13639_-143+13 others(8): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869314 | ||||||
chr5:88869316
|
C | T | 191 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(188): Show | 191 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(188): Show |
intron_variant | MODIFIER | c.-143+13639G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869316 | ||||||
chr5:88869426
|
G | A | 1 | a0001c0001t0001g0059 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-143+13529C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869426 | ||||||
chr5:88869507
|
G | C | 1 | a0001c0001t0033g0060 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-143+13448C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869507 | ||||||
chr5:88869607
|
A | G | 3 | a0001c0001t0001g0135a0001c0001t0001g0166a0001c0001t0004g0136 | 3 | HG00280.hp1 HG01070.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-143+13348T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869607 | ||||||
chr5:88869714
|
C | A | 1 | a0001c0001t0001g0061 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-143+13241G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869714 | ||||||
chr5:88869862
|
G | A | 1 | a0001c0001t0001g0097 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-143+13093C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869862 | ||||||
chr5:88869866
|
C | T | 3 | a0001c0001t0002g0023a0001c0001t0007g0017a0001c0001t0007g0018 | 3 | HG02896.hp1 HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-143+13089G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869866 | ||||||
chr5:88869958
|
T | C | 1 | a0001c0001t0002g0062 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-143+12997A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88869958 | ||||||
chr5:88870244
|
G | A | 46 | a0001c0001t0001g0190a0001c0001t0002g0182a0001c0001t0002g0183others(43): Show | 46 | HG00597.hp1 HG01243.hp2 HG01361.hp1 others(43): Show |
intron_variant | MODIFIER | c.-143+12711C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88870244 | ||||||
chr5:88870887
|
G | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG02257.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-143+12068C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88870887 | ||||||
chr5:88871458
|
C | T | 1 | a0001c0001t0002g0218 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-143+11497G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88871458 | ||||||
chr5:88871463
|
G | A | 2 | a0001c0001t0007g0300a0001c0001t0007g0301 | 2 | HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-143+11492C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88871463 | ||||||
chr5:88871605
|
T | C | 1 | a0001c0001t0004g0239 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-143+11350A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88871605 | ||||||
chr5:88871824
|
A | G | 56 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0029others(53): Show | 56 | HG00544.hp1 HG01099.hp1 HG01123.hp1 others(53): Show |
intron_variant | MODIFIER | c.-143+11131T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88871824 | ||||||
chr5:88871923
|
G | C | 198 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(195): Show | 198 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(195): Show |
intron_variant | MODIFIER | c.-143+11032C>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88871923 | ||||||
chr5:88872196
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-143+10759G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88872196 | ||||||
chr5:88872578
|
C | G | 198 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(195): Show | 198 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(195): Show |
intron_variant | MODIFIER | c.-143+10377G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88872578 | ||||||
chr5:88872580
|
C | T | 299 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(296): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.-143+10375G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88872580 | ||||||
chr5:88872681
|
T | C | 3 | a0001c0001t0001g0022a0001c0001t0001g0063a0001c0001t0001g0064 | 3 | NA18979.hp1 NA19057.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.-143+10274A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88872681 | ||||||
chr5:88872817
|
G | A | 3 | a0001c0001t0001g0072a0001c0001t0001g0077a0001c0001t0001g0078 | 3 | HG01261.hp1 HG02809.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-143+10138C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88872817 | ||||||
chr5:88872895
|
A | G | 2 | a0001c0001t0006g0133a0001c0001t0006g0134 | 2 | NA18970.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.-143+10060T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88872895 | ||||||
chr5:88872978
|
G | A | 1 | a0001c0001t0001g0024 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-143+9977C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88872978 | ||||||
chr5:88873031
|
C | T | 1 | a0001c0001t0003g0257 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-143+9924G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88873031 | ||||||
chr5:88873056
|
T | TAC | 15 | a0001c0001t0002g0232a0001c0001t0003g0255a0001c0001t0004g0239others(12): Show | 15 | HG00741.hp1 HG01496.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.-143+9897_-143+989 others(6): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88873056 | ||||||
chr5:88873138
|
C | A | 198 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(195): Show | 198 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(195): Show |
intron_variant | MODIFIER | c.-143+9817G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88873138 | ||||||
chr5:88873669
|
C | T | 1 | a0001c0001t0038g0302 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-143+9286G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88873669 | ||||||
chr5:88873708
|
A | AT | 18 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0120others(15): Show | 18 | HG00741.hp2 HG01169.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.-143+9246dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88873708 | ||||||
chr5:88873708
|
A | ATT | 11 | a0001c0001t0001g0093a0001c0001t0001g0126a0001c0001t0001g0129others(8): Show | 11 | HG01934.hp1 HG02451.hp1 HG02970.hp1 others(8): Show |
intron_variant | MODIFIER | c.-143+9245_-143+924 others(6): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88873708 | ||||||
chr5:88873708
|
AT | A | 23 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0078others(20): Show | 23 | HG00280.hp2 HG00733.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.-143+9246delA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88873708 | ||||||
chr5:88873708
|
ATT | A | 10 | a0001c0001t0001g0001a0001c0001t0001g0092a0001c0001t0001g0104others(7): Show | 10 | HG00733.hp1 HG01081.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.-143+9245_-143+924 others(6): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88873708 | ||||||
chr5:88873708
|
ATTTTTT | A | 10 | a0001c0001t0002g0232a0001c0001t0003g0238a0001c0001t0003g0242others(7): Show | 10 | HG00741.hp1 HG01934.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-143+9241_-143+924 others(10): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88873708 | ||||||
chr5:88873708
|
ATTTTTTT | A | 61 | a0001c0001t0001g0267a0001c0001t0001g0273a0001c0001t0002g0234others(58): Show | 61 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.-143+9240_-143+924 others(11): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88873708 | ||||||
chr5:88873708
|
ATTTTTTT others(1): Show |
A | 15 | a0001c0001t0001g0090a0001c0001t0001g0110a0001c0001t0002g0186others(12): Show | 15 | HG00639.hp2 HG01070.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.-143+9239_-143+924 others(12): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88873708 | ||||||
chr5:88873708
|
ATTTTTTT others(2): Show |
A | 54 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(51): Show | 54 | HG00597.hp1 HG01192.hp1 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.-143+9238_-143+924 others(13): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88873708 | ||||||
chr5:88873708
|
ATTTTTTT others(3): Show |
A | 5 | a0001c0001t0002g0023a0001c0001t0002g0215a0001c0001t0007g0017others(2): Show | 5 | HG00639.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-143+9237_-143+924 others(14): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88873708 | ||||||
chr5:88873708
|
ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0002g0216 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-143+9236_-143+924 others(15): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88873708 | ||||||
chr5:88873708
|
ATTTTTTT others(6): Show |
A | 1 | a0001c0001t0001g0024 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-143+9234_-143+924 others(17): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88873708 | ||||||
chr5:88873708
|
ATTTTTTT others(7): Show |
A | 51 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0031others(48): Show | 51 | HG00544.hp1 HG01099.hp1 HG01123.hp1 others(48): Show |
intron_variant | MODIFIER | c.-143+9233_-143+924 others(18): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88873708 | ||||||
chr5:88873750
|
A | G | 198 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(195): Show | 198 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(195): Show |
intron_variant | MODIFIER | c.-143+9205T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88873750 | ||||||
chr5:88873835
|
A | G | 198 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(195): Show | 198 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(195): Show |
intron_variant | MODIFIER | c.-143+9120T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88873835 | ||||||
chr5:88873916
|
A | G | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | NA18960.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.-143+9039T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88873916 | ||||||
chr5:88873935
|
G | A | 2 | a0001c0001t0001g0090a0001c0001t0003g0091 | 2 | HG01884.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-143+9020C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88873935 | ||||||
chr5:88874162
|
G | A | 3 | a0001c0001t0005g0013a0001c0001t0005g0014a0001c0001t0036g0015 | 3 | HG01243.hp1 HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-143+8793C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88874162 | ||||||
chr5:88874190
|
C | T | 17 | a0001c0001t0002g0234a0001c0001t0002g0243a0001c0001t0002g0244others(14): Show | 17 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.-143+8765G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88874190 | ||||||
chr5:88874226
|
C | T | 2 | a0001c0001t0004g0108a0001c0001t0030g0109 | 2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-143+8729G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88874226 | ||||||
chr5:88874249
|
T | C | 207 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(204): Show | 207 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(204): Show |
intron_variant | MODIFIER | c.-143+8706A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88874249 | ||||||
chr5:88874437
|
T | C | 1 | a0001c0001t0003g0296 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-143+8518A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88874437 | ||||||
chr5:88874514
|
T | C | 198 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(195): Show | 198 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(195): Show |
intron_variant | MODIFIER | c.-143+8441A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88874514 | ||||||
chr5:88874752
|
T | C | 2 | a0001c0001t0007g0300a0001c0001t0007g0301 | 2 | HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-143+8203A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88874752 | ||||||
chr5:88874759
|
T | C | 1 | a0001c0001t0034g0012 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-143+8196A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88874759 | ||||||
chr5:88875013
|
G | A | 2 | a0001c0001t0003g0230a0001c0001t0003g0231 | 2 | HG02486.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-143+7942C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88875013 | ||||||
chr5:88875048
|
T | A | 1 | a0001c0001t0001g0065 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-143+7907A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88875048 | ||||||
chr5:88875412
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-143+7543T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88875412 | ||||||
chr5:88875470
|
T | C | 1 | a0001c0001t0002g0174 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-143+7485A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88875470 | ||||||
chr5:88875530
|
C | G | 1 | a0001c0001t0001g0181 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-143+7425G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88875530 | ||||||
chr5:88875679
|
A | T | 1 | a0001c0001t0003g0185 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-143+7276T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88875679 | ||||||
chr5:88875817
|
C | T | 1 | a0001c0001t0002g0003 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-143+7138G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88875817 | ||||||
chr5:88875908
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-143+7047A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88875908 | ||||||
chr5:88875947
|
C | A | 2 | a0001c0001t0001g0090a0001c0001t0003g0091 | 2 | HG01884.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-143+7008G>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88875947 | ||||||
chr5:88876063
|
G | GT | 6 | a0001c0001t0001g0092a0001c0001t0001g0117a0001c0001t0001g0120others(3): Show | 6 | HG01978.hp2 HG02135.hp2 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.-143+6891dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88876063 | ||||||
chr5:88876063
|
GT | G | 126 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(123): Show | 126 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(123): Show |
intron_variant | MODIFIER | c.-143+6891delA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88876063 | ||||||
chr5:88876063
|
GTT | G | 68 | a0001c0001t0001g0267a0001c0001t0001g0273a0001c0001t0002g0232others(65): Show | 68 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(65): Show |
intron_variant | MODIFIER | c.-143+6890_-143+689 others(6): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88876063 | ||||||
chr5:88876193
|
T | C | 1 | a0001c0001t0018g0119 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-143+6762A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88876193 | ||||||
chr5:88876253
|
T | C | 1 | a0001c0001t0002g0070 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-143+6702A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88876253 | ||||||
chr5:88877014
|
A | G | 1 | a0001c0001t0001g0001 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-143+5941T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88877014 | ||||||
chr5:88877101
|
A | G | 1 | a0001c0001t0002g0232 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-143+5854T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88877101 | ||||||
chr5:88877199
|
G | A | 2 | a0001c0001t0001g0090a0001c0001t0003g0091 | 2 | HG01884.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-143+5756C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88877199 | ||||||
chr5:88877362
|
T | C | 2 | a0001c0001t0004g0108a0001c0001t0030g0109 | 2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-143+5593A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88877362 | ||||||
chr5:88877843
|
A | T | 2 | a0001c0001t0003g0230a0001c0001t0003g0231 | 2 | HG02486.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-143+5112T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88877843 | ||||||
chr5:88878027
|
C | T | 2 | a0001c0001t0002g0183a0001c0001t0008g0184 | 2 | HG00597.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-143+4928G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88878027 | ||||||
chr5:88878087
|
A | G | 1 | a0001c0001t0004g0071 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-143+4868T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88878087 | ||||||
chr5:88878959
|
A | G | 1 | a0001c0001t0007g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-143+3996T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88878959 | ||||||
chr5:88879068
|
T | C | 1 | a0001c0001t0004g0297 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-143+3887A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88879068 | ||||||
chr5:88879102
|
A | T | 1 | a0001c0001t0018g0119 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-143+3853T>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88879102 | ||||||
chr5:88879134
|
C | T | 3 | a0001c0001t0005g0013a0001c0001t0005g0014a0001c0001t0036g0015 | 3 | HG01243.hp1 HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-143+3821G>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88879134 | ||||||
chr5:88879287
|
T | C | 5 | a0001c0001t0001g0176a0001c0001t0009g0175a0001c0001t0009g0177others(2): Show | 5 | HG01928.hp1 NA18953.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.-143+3668A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88879287 | ||||||
chr5:88879382
|
TTA | T | 196 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(193): Show | 196 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(193): Show |
intron_variant | MODIFIER | c.-143+3571_-143+357 others(6): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88879382 | ||||||
chr5:88879434
|
C | G | 218 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(215): Show | 218 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(215): Show |
intron_variant | MODIFIER | c.-143+3521G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88879434 | ||||||
chr5:88879505
|
G | A | 1 | a0001c0001t0002g0217 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-143+3450C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88879505 | ||||||
chr5:88879634
|
T | C | 5 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220others(2): Show | 5 | NA18949.hp2 NA18965.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.-143+3321A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88879634 | ||||||
chr5:88879669
|
T | C | 1 | a0001c0001t0005g0298 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-143+3286A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88879669 | ||||||
chr5:88879742
|
T | C | 2 | a0001c0001t0004g0108a0001c0001t0030g0109 | 2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-143+3213A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88879742 | ||||||
chr5:88879794
|
G | T | 1 | a0001c0001t0034g0012 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-143+3161C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88879794 | ||||||
chr5:88880405
|
G | A | 1 | a0001c0001t0001g0180 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-143+2550C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88880405 | ||||||
chr5:88880482
|
T | C | 1 | a0001c0001t0002g0223 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-143+2473A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88880482 | ||||||
chr5:88880522
|
G | A | 1 | a0001c0001t0003g0299 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-143+2433C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88880522 | ||||||
chr5:88880580
|
T | C | 7 | a0001c0001t0001g0110a0001c0001t0003g0113a0001c0001t0004g0011others(4): Show | 7 | HG00639.hp2 HG01192.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.-143+2375A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88880580 | ||||||
chr5:88880618
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-143+2337C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88880618 | ||||||
chr5:88880662
|
A | G | 1 | a0001c0001t0004g0011 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-143+2293T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88880662 | ||||||
chr5:88880857
|
T | C | 2 | a0001c0001t0002g0224a0001c0001t0002g0225 | 2 | NA18944.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.-143+2098A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88880857 | ||||||
chr5:88880916
|
A | G | 1 | a0001c0001t0003g0010 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-143+2039T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88880916 | ||||||
chr5:88881044
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-143+1911C>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88881044 | ||||||
chr5:88881160
|
A | G | 1 | a0001c0001t0001g0117 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-143+1795T>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88881160 | ||||||
chr5:88881726
|
C | CT | 225 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(222): Show | 225 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(222): Show |
intron_variant | MODIFIER | c.-143+1228dupA | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88881726 | ||||||
chr5:88881726
|
C | CTT | 8 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(5): Show | 8 | HG01981.hp1 HG02257.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-143+1227_-143+122 others(6): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88881726 | ||||||
chr5:88881782
|
T | C | 46 | a0001c0001t0001g0190a0001c0001t0002g0182a0001c0001t0002g0183others(43): Show | 46 | HG00597.hp1 HG01243.hp2 HG01361.hp1 others(43): Show |
intron_variant | MODIFIER | c.-143+1173A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88881782 | ||||||
chr5:88882393
|
C | G | 1 | a0001c0001t0004g0002 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-143+562G>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88882393 | ||||||
chr5:88882653
|
T | A | 2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | HG00741.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.-143+302A>T | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88882653 | ||||||
chr5:88882672
|
G | T | 1 | a0001c0001t0001g0001 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-143+283C>A | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88882672 | ||||||
chr5:88882843
|
T | G | 1 | a0001c0001t0001g0229 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-143+112A>C | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88882843 | ||||||
chr5:88882866
|
T | C | 71 | a0001c0001t0001g0267a0001c0001t0001g0273a0001c0001t0002g0232others(68): Show | 71 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.-143+89A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88882866 | ||||||
chr5:88882911
|
T | C | 2 | a0001c0001t0007g0300a0001c0001t0007g0301 | 2 | HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-143+44A>G | MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | 88882911 |