geneid | 152586 |
---|---|
ensemblid | ENSG00000205301.12 |
hgncid | 43619 |
symbol | MGAT4D |
name | MGAT4 family member D |
refseq_nuc | NM_001277353.2 |
refseq_prot | NP_001264282.1 |
ensembl_nuc | ENST00000511113.6 |
ensembl_prot | ENSP00000421185.1 |
mane_status | MANE Select |
chr | chr4 |
start | 140442262 |
end | 140498293 |
strand | - |
ver | v1.2 |
region | chr4:140442262-140498293 |
region5000 | chr4:140437262-140503293 |
regionname0 | MGAT4D_chr4_140442262_140498293 |
regionname5000 | MGAT4D_chr4_140437262_140503293 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 374 | 218 | 65 | 37 | 92 | 4 | 19 | 68 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
a0002 | 0/1 | 374 | 104 | 17 | 23 | 48 | 2 | 13 | 37 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
a0003 | 0/0 | 374 | 5 | 0 | 0 | 5 | 0 | 0 | 4 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
a0004 | 0/0 | 374 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
a0005 | 0/0 | 374 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
a0006 | 0/0 | 318 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1125 | 216 | 64 | 37 | 92 | 3 | 19 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
c0002 | 0/0 | 1125 | 101 | 17 | 23 | 46 | 2 | 13 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
c0003 | 0/0 | 1125 | 5 | 0 | 0 | 5 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
c0004 | 0/0 | 1125 | 3 | 0 | 2 | 0 | 1 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
c0005 | 0/1 | 1125 | 3 | 0 | 0 | 2 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
c0006 | 0/0 | 1125 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
c0007 | 0/0 | 1125 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
c0008 | 0/0 | 1125 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
c0009 | 0/0 | 1125 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1242 | 146 | 27 | 32 | 70 | 4 | 13 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
t0002 | 0/0 | 1242 | 84 | 17 | 17 | 34 | 1 | 15 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
t0003 | 0/0 | 1246 | 56 | 4 | 10 | 38 | 2 | 2 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
t0004 | 0/1 | 1246 | 20 | 16 | 2 | 0 | 1 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
t0005 | 1/0 | 1246 | 12 | 10 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
t0006 | 0/0 | 1246 | 6 | 6 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
t0007 | 0/0 | 1242 | 2 | 0 | 0 | 0 | 0 | 2 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
t0008 | 0/0 | 1242 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
t0009 | 0/0 | 1246 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
t0010 | 0/0 | 1242 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
t0011 | 0/0 | 1246 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
t0012 | 0/0 | 1242 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
t0013 | 0/0 | 1242 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0081 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0123 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1125 | 216 | 64 | 37 | 92 | 3 | 19 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
a0001c0007 | 0/0 | 1125 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
a0001c0009 | 0/0 | 1125 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
a0002c0002 | 0/0 | 1125 | 101 | 17 | 23 | 46 | 2 | 13 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
a0002c0005 | 0/1 | 1125 | 3 | 0 | 0 | 2 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
a0003c0003 | 0/0 | 1125 | 5 | 0 | 0 | 5 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
a0004c0004 | 0/0 | 1125 | 3 | 0 | 2 | 0 | 1 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
a0005c0008 | 0/0 | 1125 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
a0006c0006 | 0/0 | 1125 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2366 | 137 | 26 | 31 | 65 | 2 | 13 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
a0001c0001t0002 | 0/0 | 2366 | 46 | 14 | 4 | 22 | 0 | 6 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
a0001c0001t0003 | 0/0 | 2370 | 4 | 2 | 0 | 2 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
a0001c0001t0004 | 0/0 | 2370 | 7 | 5 | 1 | 0 | 1 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
a0001c0001t0005 | 1/0 | 2370 | 12 | 10 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
a0001c0001t0006 | 0/0 | 2370 | 6 | 6 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
a0001c0001t0008 | 0/0 | 2366 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
a0001c0001t0010 | 0/0 | 2366 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
a0001c0001t0011 | 0/0 | 2370 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
a0001c0001t0013 | 0/0 | 2366 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
a0001c0007t0004 | 0/0 | 2370 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
a0001c0009t0001 | 0/0 | 2366 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
a0002c0002t0001 | 0/0 | 2366 | 5 | 1 | 1 | 3 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
a0002c0002t0002 | 0/0 | 2366 | 35 | 3 | 11 | 12 | 0 | 9 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
a0002c0002t0003 | 0/0 | 2370 | 46 | 2 | 10 | 30 | 2 | 2 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
a0002c0002t0004 | 0/0 | 2370 | 11 | 10 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
a0002c0002t0007 | 0/0 | 2366 | 2 | 0 | 0 | 0 | 0 | 2 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
a0002c0002t0009 | 0/0 | 2370 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
a0002c0002t0012 | 0/0 | 2366 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
a0002c0005t0001 | 0/0 | 2366 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
a0002c0005t0003 | 0/0 | 2370 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
a0002c0005t0004 | 0/1 | 2370 | 1 | 0 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
a0003c0003t0003 | 0/0 | 2370 | 5 | 0 | 0 | 5 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
a0004c0004t0002 | 0/0 | 2366 | 3 | 0 | 2 | 0 | 1 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
a0005c0008t0001 | 0/0 | 2366 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
a0006c0006t0001 | 0/0 | 2366 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | copy fasta | chr4 | 140437262 | 140503293 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0004g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0005g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0005g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0005g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0005g0123 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0005g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0005g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0005g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0005g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0006g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0006g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0006g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0006g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0008g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0010g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0011g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0001t0013g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0007t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0001c0009t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0004g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0007g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0009g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0002t0012g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0005t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0005t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0002c0005t0004g0081 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0003c0003t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0003c0003t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0003c0003t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0003c0003t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0003c0003t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0004c0004t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0004c0004t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0004c0004t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0005c0008t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
a0006c0006t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0103 | EUR | GBR | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG00140 | hp2 | a0001 | c0001 | t0004 | g0136 | EUR | GBR | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG00280 | hp1 | a0005 | c0008 | t0001 | g0238 | EUR | FIN | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG00280 | hp2 | a0002 | c0002 | t0003 | g0020 | EUR | FIN | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG00323 | hp1 | a0002 | c0002 | t0003 | g0022 | EUR | FIN | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0182 | EUR | FIN | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | CHS | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG00408 | hp2 | a0002 | c0002 | t0003 | g0035 | EAS | CHS | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG00438 | hp1 | a0002 | c0002 | t0003 | g0037 | EAS | CHS | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG00544 | hp1 | a0002 | c0002 | t0002 | g0257 | EAS | CHS | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0315 | EAS | CHS | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | CHS | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG00609 | hp1 | a0002 | c0002 | t0002 | g0253 | EAS | CHS | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | CHS | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG00639 | hp1 | a0002 | c0002 | t0002 | g0023 | AMR | PUR | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG00642 | hp2 | a0002 | c0002 | t0002 | g0265 | AMR | PUR | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | CHS | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG00673 | hp2 | a0002 | c0002 | t0002 | g0270 | EAS | CHS | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG00738 | hp2 | a0002 | c0002 | t0002 | g0230 | AMR | PUR | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01070 | hp2 | a0002 | c0002 | t0002 | g0269 | AMR | PUR | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01074 | hp1 | a0002 | c0002 | t0003 | g0062 | AMR | PUR | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01106 | hp2 | a0001 | c0001 | t0005 | g0066 | AMR | PUR | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01175 | hp1 | a0004 | c0004 | t0002 | g0251 | AMR | PUR | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0113 | AMR | PUR | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01192 | hp2 | a0002 | c0002 | t0004 | g0003 | AMR | PUR | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01255 | hp1 | a0002 | c0002 | t0002 | g0232 | AMR | CLM | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01255 | hp2 | a0002 | c0002 | t0002 | g0247 | AMR | CLM | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0115 | AMR | CLM | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01261 | hp1 | a0004 | c0004 | t0002 | g0263 | AMR | CLM | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01261 | hp2 | a0001 | c0001 | t0004 | g0128 | AMR | CLM | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01361 | hp2 | a0002 | c0002 | t0002 | g0231 | AMR | CLM | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01433 | hp1 | a0002 | c0002 | t0003 | g0040 | AMR | CLM | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | CLM | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01515 | hp1 | a0001 | c0009 | t0001 | g0323 | EUR | IBS | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01515 | hp2 | a0004 | c0004 | t0002 | g0246 | EUR | IBS | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01884 | hp2 | a0002 | c0002 | t0004 | g0057 | AFR | ACB | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01891 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | ACB | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01928 | hp2 | a0002 | c0002 | t0003 | g0021 | AMR | PEL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01943 | hp1 | a0002 | c0002 | t0003 | g0015 | AMR | PEL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01952 | hp1 | a0002 | c0002 | t0002 | g0254 | AMR | PEL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01952 | hp2 | a0002 | c0002 | t0003 | g0042 | AMR | PEL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01978 | hp1 | a0002 | c0002 | t0003 | g0053 | AMR | PEL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01981 | hp2 | a0002 | c0002 | t0002 | g0258 | AMR | PEL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01993 | hp2 | a0002 | c0002 | t0001 | g0245 | AMR | PEL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02004 | hp1 | a0002 | c0002 | t0003 | g0047 | AMR | PEL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02027 | hp2 | a0001 | c0001 | t0008 | g0192 | EAS | KHV | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02040 | hp1 | a0002 | c0005 | t0001 | g0083 | EAS | KHV | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02040 | hp2 | a0001 | c0001 | t0010 | g0302 | EAS | KHV | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02074 | hp1 | a0002 | c0002 | t0003 | g0032 | EAS | KHV | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | KHV | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02132 | hp2 | a0002 | c0002 | t0003 | g0027 | EAS | KHV | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02148 | hp1 | a0002 | c0002 | t0003 | g0054 | AMR | PEL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02155 | hp1 | a0002 | c0002 | t0012 | g0249 | EAS | CDX | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | CDX | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CDX | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02165 | hp2 | a0002 | c0002 | t0003 | g0010 | EAS | CDX | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0283 | AFR | ACB | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02258 | hp2 | a0002 | c0002 | t0004 | g0069 | AFR | ACB | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02273 | hp2 | a0002 | c0002 | t0003 | g0049 | AMR | PEL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02280 | hp1 | a0002 | c0002 | t0004 | g0071 | AFR | ACB | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | ACB | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02293 | hp1 | a0002 | c0002 | t0003 | g0048 | AMR | PEL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0132 | AMR | PEL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02300 | hp2 | a0002 | c0002 | t0002 | g0259 | AMR | PEL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02523 | hp2 | a0003 | c0003 | t0003 | g0024 | EAS | KHV | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0118 | AFR | GWD | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0223 | SAS | PJL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0271 | AFR | GWD | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0119 | AFR | GWD | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02622 | hp2 | a0001 | c0001 | t0006 | g0004 | AFR | GWD | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0282 | AFR | GWD | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0145 | AFR | GWD | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02647 | hp2 | a0001 | c0001 | t0005 | g0240 | AFR | GWD | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0284 | AFR | GWD | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02723 | hp1 | a0002 | c0002 | t0002 | g0235 | AFR | GWD | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | GWD | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02735 | hp2 | a0002 | c0002 | t0003 | g0050 | SAS | PJL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0322 | AFR | GWD | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02818 | hp1 | a0001 | c0001 | t0006 | g0004 | AFR | GWD | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0281 | AFR | GWD | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02886 | hp2 | a0002 | c0002 | t0004 | g0059 | AFR | GWD | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02895 | hp2 | a0002 | c0002 | t0003 | g0007 | AFR | GWD | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02896 | hp1 | a0001 | c0001 | t0005 | g0241 | AFR | GWD | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02896 | hp2 | a0001 | c0001 | t0005 | g0076 | AFR | GWD | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02897 | hp1 | a0002 | c0002 | t0003 | g0007 | AFR | GWD | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02897 | hp2 | a0001 | c0001 | t0005 | g0239 | AFR | GWD | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0148 | AFR | ESN | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03017 | hp2 | a0002 | c0002 | t0002 | g0248 | SAS | PJL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | GWD | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | MSL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03098 | hp2 | a0002 | c0002 | t0004 | g0056 | AFR | MSL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03130 | hp2 | a0002 | c0002 | t0009 | g0228 | AFR | ESN | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03139 | hp1 | a0001 | c0001 | t0005 | g0117 | AFR | ESN | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03195 | hp1 | a0001 | c0001 | t0005 | g0274 | AFR | ESN | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03195 | hp2 | a0002 | c0002 | t0004 | g0003 | AFR | ESN | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03209 | hp1 | a0001 | c0001 | t0006 | g0074 | AFR | MSL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03209 | hp2 | a0002 | c0002 | t0002 | g0234 | AFR | MSL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03225 | hp2 | a0002 | c0002 | t0004 | g0055 | AFR | MSL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0108 | SAS | PJL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03453 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | MSL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0127 | AFR | MSL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | MSL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03491 | hp1 | a0002 | c0002 | t0007 | g0001 | SAS | PJL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03492 | hp2 | a0002 | c0002 | t0007 | g0001 | SAS | PJL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0130 | AFR | ESN | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0080 | AFR | GWD | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0063 | AFR | GWD | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0318 | SAS | PJL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03710 | hp1 | a0002 | c0002 | t0003 | g0043 | SAS | PJL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03710 | hp2 | a0002 | c0002 | t0002 | g0267 | SAS | PJL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | BEB | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0129 | SAS | BEB | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0120 | SAS | BEB | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | BEB | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | BEB | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03927 | hp2 | a0002 | c0002 | t0002 | g0252 | SAS | BEB | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03942 | hp1 | a0002 | c0002 | t0002 | g0229 | SAS | BEB | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0109 | SAS | BEB | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | BEB | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG04184 | hp2 | a0002 | c0002 | t0002 | g0233 | SAS | BEB | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | STU | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG04204 | hp2 | a0002 | c0002 | t0002 | g0273 | SAS | STU | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG04228 | hp1 | a0002 | c0002 | t0002 | g0078 | SAS | STU | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG04228 | hp2 | a0002 | c0002 | t0002 | g0264 | SAS | STU | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18612 | hp1 | a0002 | c0002 | t0003 | g0029 | EAS | CHB | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | CHB | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | CHB | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18747 | hp2 | a0001 | c0001 | t0013 | g0102 | EAS | CHB | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | YRI | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18906 | hp2 | a0001 | c0001 | t0006 | g0075 | AFR | YRI | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18939 | hp2 | a0002 | c0005 | t0003 | g0082 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18942 | hp2 | a0002 | c0002 | t0002 | g0277 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18947 | hp1 | a0002 | c0002 | t0001 | g0276 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18948 | hp2 | a0002 | c0002 | t0003 | g0014 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18950 | hp1 | a0002 | c0002 | t0002 | g0278 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0285 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18954 | hp2 | a0003 | c0003 | t0003 | g0019 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18957 | hp2 | a0002 | c0002 | t0002 | g0280 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18959 | hp2 | a0002 | c0002 | t0002 | g0272 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18961 | hp2 | a0003 | c0003 | t0003 | g0012 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18975 | hp2 | a0002 | c0002 | t0003 | g0034 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18982 | hp1 | a0003 | c0003 | t0003 | g0026 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18986 | hp1 | a0002 | c0002 | t0002 | g0256 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18986 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18989 | hp1 | a0002 | c0002 | t0003 | g0060 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18989 | hp2 | a0002 | c0002 | t0003 | g0018 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18991 | hp2 | a0002 | c0002 | t0003 | g0033 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18992 | hp1 | a0002 | c0002 | t0003 | g0011 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18993 | hp1 | a0002 | c0002 | t0003 | g0016 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18998 | hp1 | a0002 | c0002 | t0002 | g0260 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18999 | hp1 | a0002 | c0002 | t0003 | g0051 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA18999 | hp2 | a0006 | c0006 | t0001 | g0177 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19004 | hp2 | a0002 | c0002 | t0003 | g0052 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19007 | hp2 | a0002 | c0002 | t0003 | g0151 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19011 | hp2 | a0002 | c0002 | t0003 | g0061 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19030 | hp1 | a0002 | c0002 | t0002 | g0072 | AFR | LWK | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | LWK | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19043 | hp1 | a0001 | c0001 | t0011 | g0320 | AFR | LWK | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | LWK | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19054 | hp2 | a0002 | c0002 | t0003 | g0017 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19056 | hp1 | a0002 | c0002 | t0003 | g0036 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19057 | hp1 | a0002 | c0002 | t0003 | g0031 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19060 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19063 | hp1 | a0002 | c0002 | t0002 | g0266 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19064 | hp1 | a0002 | c0002 | t0003 | g0039 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19068 | hp1 | a0002 | c0002 | t0003 | g0030 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19070 | hp1 | a0002 | c0002 | t0003 | g0045 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19072 | hp1 | a0002 | c0002 | t0002 | g0250 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19078 | hp1 | a0002 | c0002 | t0003 | g0013 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19080 | hp2 | a0002 | c0002 | t0002 | g0255 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19081 | hp2 | a0002 | c0002 | t0001 | g0279 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19083 | hp2 | a0003 | c0003 | t0003 | g0044 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19084 | hp2 | a0002 | c0002 | t0003 | g0046 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19086 | hp1 | a0002 | c0002 | t0003 | g0025 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19089 | hp1 | a0002 | c0002 | t0003 | g0038 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19091 | hp1 | a0002 | c0002 | t0003 | g0028 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19240 | hp1 | a0001 | c0001 | t0004 | g0275 | AFR | YRI | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0244 | AFR | YRI | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA20129 | hp1 | a0001 | c0001 | t0005 | g0243 | AFR | ASW | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ASW | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA20905 | hp1 | a0002 | c0002 | t0002 | g0268 | SAS | GIH | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | GIH | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG01123 | hp2 | a0002 | c0002 | t0002 | g0262 | AMR | CLM | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02109 | hp1 | a0002 | c0002 | t0004 | g0068 | AFR | ACB | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0225 | AFR | ACB | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02486 | hp1 | a0002 | c0002 | t0004 | g0058 | AFR | ACB | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02486 | hp2 | a0001 | c0001 | t0005 | g0116 | AFR | ACB | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG02559 | hp2 | a0001 | c0007 | t0004 | g0064 | AFR | ACB | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03471 | hp1 | a0001 | c0001 | t0004 | g0294 | AFR | MSL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
HG03471 | hp2 | a0001 | c0001 | t0005 | g0242 | AFR | MSL | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | USA | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | USA | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA21309 | hp1 | a0002 | c0002 | t0004 | g0070 | AFR | LWK | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
NA21309 | hp2 | a0002 | c0002 | t0001 | g0067 | AFR | LWK | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
homoSapiens_chm13v2 | hp1 | a0002 | c0005 | t0004 | g0081 | REF | REF | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0005 | g0123 | REF | REF | MGAT4D_chr4_140437262_140503293 | MGAT4D | chr4 | 140437262 | 140503293 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:140456640
|
C | T | 1 | a0006 | 1 | NA18999.hp2 | stop_gained | HIGH | c.957G>A | p.Trp319* | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/11 | 1028/2370 | 957/1125 | 319/374 | chr4 | 140456640 | ||
chr4:140456668
|
A | G | 1 | a0003 | 5 | HG02523.hp2 NA18954.hp2 NA18961.hp2 others(2): Show |
missense_variant | MODERATE | c.929T>C | p.Met310Thr | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/11 | 1000/2370 | 929/1125 | 310/374 | chr4 | 140456668 | ||
chr4:140459572
|
C | T | 1 | a0004 | 3 | HG01175.hp1 HG01261.hp1 HG01515.hp2 |
missense_variant | MODERATE | c.817G>A | p.Val273Ile | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 8/11 | 888/2370 | 817/1125 | 273/374 | chr4 | 140459572 | ||
chr4:140461967
|
A | T | 3 | a0002a0003a0004 | 112 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(109): Show |
missense_variant | MODERATE | c.724T>A | p.Leu242Met | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 7/11 | 795/2370 | 724/1125 | 242/374 | chr4 | 140461967 | ||
chr4:140482408
|
T | C | 1 | a0005 | 1 | HG00280.hp1 | missense_variant | MODERATE | c.172A>G | p.Lys58Glu | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/11 | 243/2370 | 172/1125 | 58/374 | chr4 | 140482408 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:140464952
|
T | C | 1 | a0002c0005 | 3 | HG02040.hp1 NA18939.hp2 homoSapiens_chm13v2.hp1 |
synonymous_variant | LOW | c.630A>G | p.Leu210Leu | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 6/11 | 701/2370 | 630/1125 | 210/374 | chr4 | 140464952 | ||
chr4:140482337
|
T | A | 1 | a0001c0007 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.243A>T | p.Ser81Ser | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/11 | 314/2370 | 243/1125 | 81/374 | chr4 | 140482337 | ||
chr4:140498166
|
G | A | 1 | a0001c0009 | 1 | HG01515.hp1 | synonymous_variant | LOW | c.57C>T | p.Ser19Ser | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/11 | 128/2370 | 57/1125 | 19/374 | chr4 | 140498166 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:140442514
|
A | G | 1 | a0001c0001t0006 | 6 | HG01891.hp1 HG02622.hp2 HG02818.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*922T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 11/11 | 922 | chr4 | 140442514 | |||||
chr4:140442750
|
G | T | 1 | a0001c0001t0006 | 6 | HG01891.hp1 HG02622.hp2 HG02818.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*686C>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 11/11 | 686 | chr4 | 140442750 | |||||
chr4:140442755
|
A | C | 1 | a0001c0001t0006 | 6 | HG01891.hp1 HG02622.hp2 HG02818.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*681T>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 11/11 | 681 | chr4 | 140442755 | |||||
chr4:140442838
|
CTGTG | C | 9 | a0001c0001t0001a0001c0001t0008a0001c0001t0010others(6): Show | 150 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*594_*597delCACA | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 11/11 | 594 | chr4 | 140442838 | |||||
chr4:140442907
|
T | C | 1 | a0002c0002t0009 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*529A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 11/11 | 529 | chr4 | 140442907 | |||||
chr4:140442982
|
T | A | 20 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(17): Show | 299 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(296): Show |
3_prime_UTR_variant | MODIFIER | c.*454A>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 11/11 | 454 | chr4 | 140442982 | |||||
chr4:140443013
|
C | G | 1 | a0001c0001t0008 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*423G>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 11/11 | 423 | chr4 | 140443013 | |||||
chr4:140443134
|
T | C | 5 | a0001c0001t0002a0001c0001t0013a0002c0002t0002others(2): Show | 86 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*302A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 11/11 | 302 | chr4 | 140443134 | |||||
chr4:140443179
|
G | A | 25 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(22): Show | 320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
3_prime_UTR_variant | MODIFIER | c.*257C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 11/11 | 257 | chr4 | 140443179 | |||||
chr4:140443192
|
T | A | 1 | a0001c0001t0010 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*244A>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 11/11 | 244 | chr4 | 140443192 | |||||
chr4:140443199
|
A | C | 1 | a0002c0002t0012 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*237T>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 11/11 | 237 | chr4 | 140443199 | |||||
chr4:140443355
|
T | C | 1 | a0002c0002t0007 | 2 | HG03491.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*81A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 11/11 | 81 | chr4 | 140443355 | |||||
chr4:140443416
|
G | C | 1 | a0001c0001t0011 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*20C>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 11/11 | 20 | chr4 | 140443416 | |||||
chr4:140443425
|
CTTAT | C | 5 | a0001c0001t0002a0001c0001t0013a0002c0002t0002others(2): Show | 86 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*7_*10delATAA | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 11/11 | 7 | chr4 | 140443425 | |||||
chr4:140443434
|
C | A | 1 | a0001c0001t0013 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2G>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 11/11 | 2 | chr4 | 140443434 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:140443494
|
T | A | 2 | a0001c0001t0004g0275a0001c0007t0004g0064 | 2 | HG02559.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1117-50A>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140443494 | ||||||
chr4:140444032
|
T | C | 1 | a0001c0001t0001g0222 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1117-588A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140444032 | ||||||
chr4:140444218
|
T | A | 1 | a0001c0001t0002g0108 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1117-774A>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140444218 | ||||||
chr4:140444232
|
T | C | 1 | a0001c0001t0001g0321 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1117-788A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140444232 | ||||||
chr4:140444338
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1117-894C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140444338 | ||||||
chr4:140444507
|
T | A | 2 | a0001c0001t0001g0090a0001c0001t0001g0165 | 2 | NA18970.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.1117-1063A>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140444507 | ||||||
chr4:140444553
|
G | A | 2 | a0001c0001t0004g0145a0001c0001t0004g0294 | 2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1117-1109C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140444553 | ||||||
chr4:140444712
|
T | A | 1 | a0001c0001t0005g0240 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1117-1268A>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140444712 | ||||||
chr4:140444716
|
T | C | 2 | a0001c0001t0004g0145a0001c0001t0004g0294 | 2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1117-1272A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140444716 | ||||||
chr4:140444757
|
A | C | 4 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(1): Show | 4 | NA18947.hp2 NA18966.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.1117-1313T>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140444757 | ||||||
chr4:140444791
|
C | A | 3 | a0002c0002t0002g0277a0002c0002t0002g0278a0002c0002t0002g0280 | 3 | NA18942.hp2 NA18950.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.1117-1347G>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140444791 | ||||||
chr4:140444887
|
C | CT | 293 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0065others(290): Show | 301 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(298): Show |
intron_variant | MODIFIER | c.1117-1444dupA | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140444887 | ||||||
chr4:140445038
|
C | T | 1 | a0001c0001t0001g0319 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1117-1594G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140445038 | ||||||
chr4:140445054
|
G | GTA | 147 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0065others(144): Show | 150 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.1117-1612_1117-161 others(6): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140445054 | ||||||
chr4:140445105
|
G | C | 15 | a0001c0001t0004g0118a0001c0001t0004g0127a0001c0001t0004g0128others(12): Show | 16 | HG01192.hp2 HG01261.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1117-1661C>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140445105 | ||||||
chr4:140445489
|
C | G | 1 | a0001c0001t0001g0224 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1117-2045G>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140445489 | ||||||
chr4:140445744
|
C | T | 53 | a0001c0001t0003g0236a0001c0001t0003g0285a0002c0002t0003g0002others(50): Show | 55 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.1117-2300G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140445744 | ||||||
chr4:140446123
|
G | GT | 93 | a0001c0001t0002g0009a0001c0001t0002g0063a0001c0001t0002g0098others(90): Show | 96 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.1117-2680dupA | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140446123 | ||||||
chr4:140446125
|
T | TC | 200 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0065others(197): Show | 205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1117-2682_1117-268 others(5): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140446125 | ||||||
chr4:140446128
|
T | TG | 13 | a0001c0001t0004g0118a0001c0001t0004g0127a0001c0001t0004g0128others(10): Show | 14 | HG01192.hp2 HG01261.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1117-2685_1117-268 others(5): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140446128 | ||||||
chr4:140446219
|
T | C | 15 | a0001c0001t0004g0118a0001c0001t0004g0127a0001c0001t0004g0128others(12): Show | 16 | HG01192.hp2 HG01261.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1117-2775A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140446219 | ||||||
chr4:140446286
|
T | C | 91 | a0001c0001t0002g0009a0001c0001t0002g0063a0001c0001t0002g0098others(88): Show | 94 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.1117-2842A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140446286 | ||||||
chr4:140446435
|
A | G | 311 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0065others(308): Show | 320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.1117-2991T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140446435 | ||||||
chr4:140446455
|
T | C | 293 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0065others(290): Show | 301 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(298): Show |
intron_variant | MODIFIER | c.1117-3011A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140446455 | ||||||
chr4:140446472
|
G | A | 2 | a0001c0001t0003g0080a0001c0001t0003g0225 | 2 | HG02109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1117-3028C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140446472 | ||||||
chr4:140446473
|
T | C | 1 | a0002c0002t0003g0060 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1117-3029A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140446473 | ||||||
chr4:140446596
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1117-3152A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140446596 | ||||||
chr4:140446614
|
A | G | 2 | a0001c0001t0004g0145a0001c0001t0004g0294 | 2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1117-3170T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140446614 | ||||||
chr4:140446742
|
A | G | 1 | a0004c0004t0002g0251 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1117-3298T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140446742 | ||||||
chr4:140446743
|
G | GT | 6 | a0001c0001t0001g0008a0001c0001t0001g0077a0001c0001t0001g0137others(3): Show | 7 | HG01358.hp2 HG03098.hp2 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.1117-3300dupA | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140446743 | ||||||
chr4:140446743
|
G | GTT | 7 | a0001c0001t0001g0073a0001c0001t0001g0166a0001c0001t0001g0201others(4): Show | 7 | HG00741.hp1 HG00741.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1117-3301_1117-330 others(6): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140446743 | ||||||
chr4:140446743
|
G | GTTT | 7 | a0001c0001t0001g0065a0001c0001t0001g0150a0001c0001t0001g0153others(4): Show | 7 | HG00639.hp2 HG01884.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1117-3302_1117-330 others(7): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140446743 | ||||||
chr4:140446743
|
G | GTTTTTTT others(3): Show |
1 | a0001c0001t0004g0275 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1117-3309_1117-330 others(14): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140446743 | ||||||
chr4:140446743
|
GT | G | 54 | a0001c0001t0001g0006a0001c0001t0001g0086a0001c0001t0001g0087others(51): Show | 56 | HG00140.hp2 HG00323.hp2 HG01106.hp1 others(53): Show |
intron_variant | MODIFIER | c.1117-3300delA | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140446743 | ||||||
chr4:140446743
|
GTT | G | 58 | a0001c0001t0001g0079a0001c0001t0001g0084a0001c0001t0001g0089others(55): Show | 59 | HG00140.hp1 HG00280.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.1117-3301_1117-330 others(6): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140446743 | ||||||
chr4:140446743
|
GTTT | G | 8 | a0001c0001t0001g0088a0001c0001t0001g0112a0001c0001t0001g0134others(5): Show | 8 | HG01884.hp1 HG02451.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1117-3302_1117-330 others(7): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140446743 | ||||||
chr4:140446743
|
GTTTTTT | G | 10 | a0001c0001t0003g0236a0002c0002t0003g0014a0002c0002t0003g0032others(7): Show | 10 | HG00438.hp1 HG01978.hp1 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.1117-3305_1117-330 others(10): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140446743 | ||||||
chr4:140446743
|
GTTTTTTT | G | 18 | a0001c0001t0003g0285a0002c0002t0003g0007a0002c0002t0003g0010others(15): Show | 19 | HG00408.hp2 HG01433.hp1 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.1117-3306_1117-330 others(11): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140446743 | ||||||
chr4:140446743
|
GTTTTTTT others(1): Show |
G | 19 | a0001c0001t0001g0141a0002c0002t0003g0002a0002c0002t0003g0013others(16): Show | 20 | HG00280.hp2 HG00323.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1117-3307_1117-330 others(12): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140446743 | ||||||
chr4:140446743
|
GTTTTTTT others(3): Show |
G | 4 | a0001c0001t0006g0004a0001c0001t0006g0005a0001c0001t0006g0074others(1): Show | 6 | HG01891.hp1 HG02622.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1117-3309_1117-330 others(14): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140446743 | ||||||
chr4:140446743
|
GTTTTTTT others(4): Show |
G | 10 | a0001c0001t0002g0126a0001c0001t0002g0129a0001c0001t0002g0130others(7): Show | 10 | HG00738.hp2 HG01255.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.1117-3310_1117-330 others(15): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140446743 | ||||||
chr4:140446743
|
GTTTTTTT others(5): Show |
G | 21 | a0001c0001t0002g0098a0001c0001t0002g0113a0001c0001t0002g0114others(18): Show | 21 | HG00673.hp2 HG01123.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.1117-3311_1117-330 others(16): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140446743 | ||||||
chr4:140446743
|
GTTTTTTT others(6): Show |
G | 55 | a0001c0001t0002g0009a0001c0001t0002g0063a0001c0001t0002g0108others(52): Show | 56 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.1117-3312_1117-330 others(17): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140446743 | ||||||
chr4:140446743
|
GTTTTTTT others(7): Show |
G | 1 | a0002c0002t0002g0269 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1117-3313_1117-330 others(18): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140446743 | ||||||
chr4:140446743
|
GTTTTTTT others(12): Show |
G | 1 | a0001c0001t0011g0320 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1117-3318_1117-330 others(23): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140446743 | ||||||
chr4:140446749
|
T | G | 1 | a0001c0001t0001g0183 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1117-3305A>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140446749 | ||||||
chr4:140446754
|
T | G | 1 | a0002c0005t0003g0082 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1117-3310A>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140446754 | ||||||
chr4:140446840
|
T | C | 1 | a0001c0001t0002g0133 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1117-3396A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140446840 | ||||||
chr4:140447162
|
T | G | 1 | a0001c0001t0005g0076 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1117-3718A>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140447162 | ||||||
chr4:140447406
|
T | C | 291 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0065others(288): Show | 299 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.1117-3962A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140447406 | ||||||
chr4:140447448
|
C | T | 13 | a0001c0001t0004g0118a0001c0001t0004g0127a0001c0001t0004g0128others(10): Show | 14 | HG01192.hp2 HG01261.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1116+3962G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140447448 | ||||||
chr4:140447485
|
G | T | 1 | a0001c0001t0001g0101 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1116+3925C>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140447485 | ||||||
chr4:140447842
|
C | T | 1 | a0001c0001t0005g0076 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1116+3568G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140447842 | ||||||
chr4:140447867
|
C | A | 2 | a0001c0001t0001g0189a0001c0001t0001g0197 | 2 | HG01074.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1116+3543G>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140447867 | ||||||
chr4:140448104
|
G | A | 2 | a0001c0001t0003g0080a0001c0001t0003g0225 | 2 | HG02109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1116+3306C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140448104 | ||||||
chr4:140448167
|
C | T | 291 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0065others(288): Show | 299 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.1116+3243G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140448167 | ||||||
chr4:140448299
|
C | A | 2 | a0001c0001t0002g0063a0001c0001t0002g0271 | 2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1116+3111G>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140448299 | ||||||
chr4:140448312
|
T | G | 2 | a0001c0001t0002g0063a0001c0001t0002g0271 | 2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1116+3098A>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140448312 | ||||||
chr4:140448357
|
C | T | 12 | a0001c0001t0001g0303a0001c0001t0001g0304a0001c0001t0001g0305others(9): Show | 12 | HG02155.hp2 NA18960.hp2 NA18979.hp2 others(9): Show |
intron_variant | MODIFIER | c.1116+3053G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140448357 | ||||||
chr4:140448517
|
A | G | 2 | a0001c0001t0004g0118a0001c0001t0004g0128 | 2 | HG01261.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1116+2893T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140448517 | ||||||
chr4:140448569
|
A | C | 2 | a0001c0001t0001g0206a0001c0001t0001g0215 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1116+2841T>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140448569 | ||||||
chr4:140448585
|
C | T | 2 | a0002c0002t0003g0007a0002c0002t0009g0228 | 3 | HG02895.hp2 HG02897.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1116+2825G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140448585 | ||||||
chr4:140448672
|
C | T | 1 | a0001c0001t0002g0271 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1116+2738G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140448672 | ||||||
chr4:140448869
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1116+2541A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140448869 | ||||||
chr4:140448871
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1116+2539A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140448871 | ||||||
chr4:140449045
|
T | G | 2 | a0001c0001t0004g0275a0001c0007t0004g0064 | 2 | HG02559.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1116+2365A>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140449045 | ||||||
chr4:140449056
|
C | A | 1 | a0002c0002t0002g0266 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1116+2354G>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140449056 | ||||||
chr4:140449058
|
C | A | 2 | a0001c0001t0004g0275a0001c0007t0004g0064 | 2 | HG02559.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1116+2352G>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140449058 | ||||||
chr4:140449299
|
G | C | 6 | a0001c0001t0001g0077a0001c0001t0001g0168a0001c0001t0001g0184others(3): Show | 6 | HG02080.hp1 NA18950.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.1116+2111C>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140449299 | ||||||
chr4:140449489
|
A | G | 1 | a0002c0002t0002g0272 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1116+1921T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140449489 | ||||||
chr4:140449587
|
G | A | 53 | a0001c0001t0003g0236a0001c0001t0003g0285a0002c0002t0003g0002others(50): Show | 55 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.1116+1823C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140449587 | ||||||
chr4:140449617
|
C | T | 1 | a0002c0002t0001g0245 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1116+1793G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140449617 | ||||||
chr4:140449618
|
G | A | 147 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0065others(144): Show | 150 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.1116+1792C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140449618 | ||||||
chr4:140449668
|
G | A | 291 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0065others(288): Show | 299 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.1116+1742C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140449668 | ||||||
chr4:140449759
|
CA | C | 289 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0065others(286): Show | 297 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.1116+1650delT | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140449759 | ||||||
chr4:140449966
|
T | C | 15 | a0001c0001t0004g0118a0001c0001t0004g0127a0001c0001t0004g0128others(12): Show | 16 | HG01192.hp2 HG01261.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1116+1444A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140449966 | ||||||
chr4:140450108
|
C | A | 1 | a0001c0001t0001g0103 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1116+1302G>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140450108 | ||||||
chr4:140450166
|
T | A | 85 | a0001c0001t0002g0009a0001c0001t0002g0063a0001c0001t0002g0098others(82): Show | 86 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.1116+1244A>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140450166 | ||||||
chr4:140450343
|
C | T | 2 | a0002c0002t0002g0277a0002c0002t0002g0280 | 2 | NA18942.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.1116+1067G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140450343 | ||||||
chr4:140450351
|
T | C | 2 | a0001c0001t0003g0080a0001c0001t0003g0225 | 2 | HG02109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1116+1059A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140450351 | ||||||
chr4:140450473
|
C | A | 200 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0065others(197): Show | 205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1116+937G>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140450473 | ||||||
chr4:140450610
|
A | C | 146 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0073others(143): Show | 149 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.1116+800T>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140450610 | ||||||
chr4:140450904
|
G | A | 85 | a0001c0001t0002g0009a0001c0001t0002g0063a0001c0001t0002g0098others(82): Show | 86 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.1116+506C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140450904 | ||||||
chr4:140450977
|
C | T | 306 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0065others(303): Show | 315 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(312): Show |
intron_variant | MODIFIER | c.1116+433G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140450977 | ||||||
chr4:140451004
|
C | T | 200 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0065others(197): Show | 205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1116+406G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140451004 | ||||||
chr4:140451081
|
T | C | 200 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0065others(197): Show | 205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1116+329A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140451081 | ||||||
chr4:140451214
|
G | A | 14 | a0001c0001t0001g0287a0001c0001t0001g0299a0001c0001t0001g0303others(11): Show | 14 | HG02071.hp2 HG02155.hp2 NA18747.hp1 others(11): Show |
intron_variant | MODIFIER | c.1116+196C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140451214 | ||||||
chr4:140451230
|
C | A | 85 | a0001c0001t0002g0009a0001c0001t0002g0063a0001c0001t0002g0098others(82): Show | 86 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.1116+180G>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140451230 | ||||||
chr4:140451331
|
T | C | 200 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0065others(197): Show | 205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1116+79A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140451331 | ||||||
chr4:140451376
|
T | C | 15 | a0001c0001t0004g0118a0001c0001t0004g0127a0001c0001t0004g0128others(12): Show | 16 | HG01192.hp2 HG01261.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1116+34A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 10/10 | chr4 | 140451376 | ||||||
chr4:140451737
|
C | T | 4 | a0001c0001t0006g0004a0001c0001t0006g0005a0001c0001t0006g0074others(1): Show | 6 | HG01891.hp1 HG02622.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1009-220G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140451737 | ||||||
chr4:140451738
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1009-221A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140451738 | ||||||
chr4:140451757
|
T | A | 1 | a0001c0001t0001g0065 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1009-240A>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140451757 | ||||||
chr4:140451883
|
A | G | 3 | a0001c0001t0002g0108a0001c0001t0002g0109a0002c0002t0002g0248 | 3 | HG03017.hp2 HG03239.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1009-366T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140451883 | ||||||
chr4:140451994
|
CA | C | 79 | a0001c0001t0002g0009a0001c0001t0002g0098a0001c0001t0002g0108others(76): Show | 81 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.1009-478delT | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140451994 | ||||||
chr4:140451994
|
CAA | C | 197 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0065others(194): Show | 204 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.1009-479_1009-478d others(4): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140451994 | ||||||
chr4:140451994
|
CAAA | C | 15 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0001g0092others(12): Show | 15 | HG01884.hp1 HG02451.hp2 HG02809.hp1 others(12): Show |
intron_variant | MODIFIER | c.1009-480_1009-478d others(5): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140451994 | ||||||
chr4:140451997
|
A | C | 20 | a0001c0001t0002g0063a0001c0001t0002g0113a0001c0001t0002g0114others(17): Show | 20 | HG00639.hp1 HG01192.hp1 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.1009-480T>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140451997 | ||||||
chr4:140451998
|
A | C | 66 | a0001c0001t0002g0009a0001c0001t0002g0098a0001c0001t0002g0108others(63): Show | 67 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.1009-481T>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140451998 | ||||||
chr4:140451999
|
A | C | 188 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0065others(185): Show | 195 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.1009-482T>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140451999 | ||||||
chr4:140452000
|
A | C | 15 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0001g0092others(12): Show | 15 | HG01884.hp1 HG02451.hp2 HG02809.hp1 others(12): Show |
intron_variant | MODIFIER | c.1009-483T>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140452000 | ||||||
chr4:140452001
|
A | C | 2 | a0001c0001t0003g0080a0001c0001t0003g0225 | 2 | HG02109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1009-484T>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140452001 | ||||||
chr4:140452002
|
A | C | 1 | a0001c0001t0001g0208 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1009-485T>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140452002 | ||||||
chr4:140452060
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1009-543C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140452060 | ||||||
chr4:140452060
|
G | C | 1 | a0001c0001t0001g0261 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1009-543C>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140452060 | ||||||
chr4:140452143
|
G | A | 1 | a0001c0001t0005g0076 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1009-626C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140452143 | ||||||
chr4:140452205
|
C | T | 2 | a0001c0001t0004g0136a0002c0005t0004g0081 | 2 | HG00140.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1009-688G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140452205 | ||||||
chr4:140452286
|
C | T | 85 | a0001c0001t0002g0009a0001c0001t0002g0063a0001c0001t0002g0098others(82): Show | 86 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.1009-769G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140452286 | ||||||
chr4:140452812
|
A | T | 2 | a0001c0001t0004g0145a0001c0001t0004g0294 | 2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1009-1295T>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140452812 | ||||||
chr4:140452869
|
AGTGTTTA others(15): Show |
A | 1 | a0003c0003t0003g0024 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1009-1374_1009-135 others(26): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140452869 | ||||||
chr4:140452915
|
T | A | 13 | a0001c0001t0004g0118a0001c0001t0004g0127a0001c0001t0004g0128others(10): Show | 14 | HG01192.hp2 HG01261.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1009-1398A>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140452915 | ||||||
chr4:140452932
|
A | G | 4 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0205others(1): Show | 4 | HG00323.hp2 HG01175.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.1009-1415T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140452932 | ||||||
chr4:140453002
|
A | G | 85 | a0001c0001t0002g0009a0001c0001t0002g0063a0001c0001t0002g0098others(82): Show | 86 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.1009-1485T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140453002 | ||||||
chr4:140453330
|
A | C | 162 | a0001c0001t0001g0073a0001c0001t0001g0085a0001c0001t0001g0086others(159): Show | 168 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.1009-1813T>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140453330 | ||||||
chr4:140453679
|
C | G | 2 | a0001c0001t0002g0271a0001c0001t0004g0294 | 2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1009-2162G>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140453679 | ||||||
chr4:140453715
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1009-2198G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140453715 | ||||||
chr4:140453786
|
A | G | 8 | a0001c0001t0005g0076a0001c0001t0011g0320a0002c0002t0004g0003others(5): Show | 9 | HG01192.hp2 HG01884.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1009-2269T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140453786 | ||||||
chr4:140453807
|
G | A | 3 | a0002c0002t0002g0230a0002c0002t0002g0231a0002c0002t0002g0232 | 3 | HG00738.hp2 HG01255.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1009-2290C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140453807 | ||||||
chr4:140453906
|
G | T | 1 | a0001c0007t0004g0064 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1009-2389C>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140453906 | ||||||
chr4:140454012
|
A | ATG | 18 | a0001c0001t0001g0065a0001c0001t0001g0085a0001c0001t0001g0086others(15): Show | 18 | HG00323.hp2 HG01070.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.1009-2497_1009-249 others(6): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140454012 | ||||||
chr4:140454012
|
A | ATGTG | 65 | a0001c0001t0001g0224a0001c0001t0001g0287a0001c0001t0001g0299others(62): Show | 66 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.1009-2499_1009-249 others(8): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140454012 | ||||||
chr4:140454012
|
A | ATGTGTG | 8 | a0001c0001t0002g0098a0001c0001t0002g0282a0001c0001t0002g0290others(5): Show | 8 | HG00673.hp1 HG00673.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1009-2501_1009-249 others(10): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140454012 | ||||||
chr4:140454012
|
ATG | A | 70 | a0002c0002t0001g0041a0002c0002t0002g0023a0002c0002t0002g0072others(67): Show | 73 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.1009-2497_1009-249 others(6): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140454012 | ||||||
chr4:140454274
|
C | T | 1 | a0001c0001t0002g0271 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1008+2315G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140454274 | ||||||
chr4:140454457
|
A | G | 10 | a0001c0001t0001g0090a0001c0001t0001g0110a0001c0001t0001g0138others(7): Show | 10 | HG01928.hp1 HG01943.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.1008+2132T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140454457 | ||||||
chr4:140454573
|
G | A | 32 | a0002c0002t0001g0245a0002c0002t0001g0276a0002c0002t0001g0279others(29): Show | 32 | HG00544.hp1 HG00609.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.1008+2016C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140454573 | ||||||
chr4:140454668
|
C | T | 76 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0002g0023others(73): Show | 80 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.1008+1921G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140454668 | ||||||
chr4:140454871
|
A | T | 76 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0002g0023others(73): Show | 80 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.1008+1718T>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140454871 | ||||||
chr4:140454897
|
TGGAA | T | 108 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0001g0245others(105): Show | 112 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.1008+1688_1008+169 others(8): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140454897 | ||||||
chr4:140454902
|
A | T | 108 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0001g0245others(105): Show | 112 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.1008+1687T>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140454902 | ||||||
chr4:140454904
|
T | C | 17 | a0002c0002t0001g0067a0002c0002t0002g0023a0002c0002t0002g0072others(14): Show | 18 | HG00639.hp1 HG00738.hp2 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.1008+1685A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140454904 | ||||||
chr4:140454941
|
ACTTT | A | 76 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0002g0023others(73): Show | 80 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.1008+1644_1008+164 others(8): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140454941 | ||||||
chr4:140454963
|
C | T | 37 | a0001c0001t0001g0287a0001c0001t0001g0299a0001c0001t0001g0303others(34): Show | 38 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.1008+1626G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140454963 | ||||||
chr4:140455088
|
T | C | 2 | a0001c0001t0001g0206a0001c0001t0001g0215 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1008+1501A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140455088 | ||||||
chr4:140455104
|
C | T | 1 | a0001c0001t0010g0302 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1008+1485G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140455104 | ||||||
chr4:140455109
|
C | T | 2 | a0001c0001t0001g0180a0001c0001t0001g0218 | 2 | HG01175.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1008+1480G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140455109 | ||||||
chr4:140455119
|
T | C | 106 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0001g0245others(103): Show | 110 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.1008+1470A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140455119 | ||||||
chr4:140455162
|
T | C | 1 | a0001c0001t0002g0125 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1008+1427A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140455162 | ||||||
chr4:140455182
|
T | G | 1 | a0001c0001t0001g0174 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1008+1407A>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140455182 | ||||||
chr4:140455260
|
G | A | 1 | a0001c0001t0013g0102 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1008+1329C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140455260 | ||||||
chr4:140455589
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG01070.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1008+1000C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140455589 | ||||||
chr4:140455643
|
C | T | 76 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0002g0023others(73): Show | 80 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.1008+946G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140455643 | ||||||
chr4:140455695
|
T | C | 3 | a0001c0001t0001g0165a0001c0001t0001g0295a0001c0001t0001g0319 | 3 | HG02074.hp2 HG02083.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.1008+894A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140455695 | ||||||
chr4:140455759
|
A | G | 5 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0002g0126others(2): Show | 5 | HG02280.hp2 HG02965.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1008+830T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140455759 | ||||||
chr4:140456114
|
G | A | 11 | a0002c0002t0003g0002a0002c0002t0003g0013a0002c0002t0003g0045others(8): Show | 12 | HG01978.hp1 HG02004.hp1 HG02148.hp1 others(9): Show |
intron_variant | MODIFIER | c.1008+475C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140456114 | ||||||
chr4:140456536
|
G | A | 76 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0002g0023others(73): Show | 80 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.1008+53C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140456536 | ||||||
chr4:140456548
|
T | G | 1 | a0001c0001t0005g0242 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1008+41A>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140456548 | ||||||
chr4:140456561
|
A | C | 7 | a0001c0001t0001g0094a0001c0001t0001g0155a0001c0001t0001g0158others(4): Show | 7 | HG02572.hp2 HG02809.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1008+28T>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 9/10 | chr4 | 140456561 | ||||||
chr4:140456846
|
C | T | 76 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0002g0023others(73): Show | 80 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.878-127G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 8/10 | chr4 | 140456846 | ||||||
chr4:140456888
|
T | C | 1 | a0001c0001t0002g0300 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.878-169A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 8/10 | chr4 | 140456888 | ||||||
chr4:140456974
|
C | A | 76 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0002g0023others(73): Show | 80 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.878-255G>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 8/10 | chr4 | 140456974 | ||||||
chr4:140457317
|
C | G | 1 | a0001c0001t0001g0220 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.878-598G>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 8/10 | chr4 | 140457317 | ||||||
chr4:140457329
|
A | T | 32 | a0002c0002t0001g0245a0002c0002t0001g0276a0002c0002t0001g0279others(29): Show | 32 | HG00544.hp1 HG00609.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.878-610T>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 8/10 | chr4 | 140457329 | ||||||
chr4:140457349
|
C | T | 76 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0002g0023others(73): Show | 80 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.878-630G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 8/10 | chr4 | 140457349 | ||||||
chr4:140457377
|
C | A | 108 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0001g0245others(105): Show | 112 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.878-658G>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 8/10 | chr4 | 140457377 | ||||||
chr4:140457739
|
C | A | 1 | a0001c0001t0001g0161 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.878-1020G>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 8/10 | chr4 | 140457739 | ||||||
chr4:140457824
|
C | T | 76 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0002g0023others(73): Show | 80 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.878-1105G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 8/10 | chr4 | 140457824 | ||||||
chr4:140458110
|
T | A | 1 | a0001c0007t0004g0064 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.878-1391A>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 8/10 | chr4 | 140458110 | ||||||
chr4:140458160
|
T | C | 76 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0002g0023others(73): Show | 80 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.877+1352A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 8/10 | chr4 | 140458160 | ||||||
chr4:140458316
|
G | GT | 108 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0001g0245others(105): Show | 112 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.877+1195_877+1196i others(3): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 8/10 | chr4 | 140458316 | ||||||
chr4:140458505
|
C | T | 4 | a0002c0002t0003g0016a0002c0002t0003g0017a0002c0002t0003g0018others(1): Show | 4 | NA18989.hp1 NA18989.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.877+1007G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 8/10 | chr4 | 140458505 | ||||||
chr4:140458526
|
T | C | 3 | a0002c0005t0001g0083a0002c0005t0003g0082a0002c0005t0004g0081 | 3 | HG02040.hp1 NA18939.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.877+986A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 8/10 | chr4 | 140458526 | ||||||
chr4:140458757
|
T | C | 73 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0002g0023others(70): Show | 77 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.877+755A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 8/10 | chr4 | 140458757 | ||||||
chr4:140458879
|
G | C | 1 | a0001c0001t0006g0075 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.877+633C>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 8/10 | chr4 | 140458879 | ||||||
chr4:140458913
|
G | A | 3 | a0001c0001t0001g0160a0001c0001t0001g0173a0001c0001t0002g0170 | 3 | HG02027.hp1 HG02165.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.877+599C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 8/10 | chr4 | 140458913 | ||||||
chr4:140458946
|
A | T | 1 | a0001c0001t0001g0163 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.877+566T>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 8/10 | chr4 | 140458946 | ||||||
chr4:140458958
|
A | C | 73 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0002g0023others(70): Show | 77 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.877+554T>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 8/10 | chr4 | 140458958 | ||||||
chr4:140458975
|
T | C | 2 | a0001c0001t0003g0080a0001c0001t0005g0117 | 2 | HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.877+537A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 8/10 | chr4 | 140458975 | ||||||
chr4:140459083
|
T | A | 76 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0002g0023others(73): Show | 80 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.877+429A>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 8/10 | chr4 | 140459083 | ||||||
chr4:140459280
|
C | A | 76 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0002g0023others(73): Show | 80 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.877+232G>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 8/10 | chr4 | 140459280 | ||||||
chr4:140459284
|
T | C | 3 | a0002c0005t0001g0083a0002c0005t0003g0082a0002c0005t0004g0081 | 3 | HG02040.hp1 NA18939.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.877+228A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 8/10 | chr4 | 140459284 | ||||||
chr4:140459630
|
A | G | 5 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(2): Show | 5 | HG00140.hp1 HG01106.hp1 HG01169.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.763-4T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 7/10 | chr4 | 140459630 | ||||||
chr4:140459768
|
T | G | 11 | a0001c0001t0001g0006a0001c0001t0001g0073a0001c0001t0001g0131others(8): Show | 14 | HG01243.hp1 HG01261.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.763-142A>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 7/10 | chr4 | 140459768 | ||||||
chr4:140459799
|
C | CT | 24 | a0001c0001t0001g0006a0001c0001t0001g0073a0001c0001t0001g0094others(21): Show | 27 | HG00544.hp2 HG01106.hp1 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.763-174dupA | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 7/10 | chr4 | 140459799 | ||||||
chr4:140459799
|
CT | C | 14 | a0001c0001t0001g0095a0002c0002t0002g0229a0002c0002t0002g0250others(11): Show | 15 | HG01978.hp1 HG02004.hp1 HG02148.hp1 others(12): Show |
intron_variant | MODIFIER | c.763-174delA | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 7/10 | chr4 | 140459799 | ||||||
chr4:140459799
|
CTT | C | 60 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0002g0023others(57): Show | 63 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.763-175_763-174del others(2): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 7/10 | chr4 | 140459799 | ||||||
chr4:140459880
|
G | T | 1 | a0001c0001t0001g0313 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.763-254C>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 7/10 | chr4 | 140459880 | ||||||
chr4:140459886
|
C | T | 76 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0002g0023others(73): Show | 80 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.763-260G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 7/10 | chr4 | 140459886 | ||||||
chr4:140459965
|
T | A | 2 | a0001c0001t0002g0297a0001c0001t0002g0298 | 2 | NA18966.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.763-339A>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 7/10 | chr4 | 140459965 | ||||||
chr4:140460102
|
G | A | 3 | a0002c0002t0003g0013a0002c0002t0003g0046a0002c0002t0003g0052 | 3 | NA19004.hp2 NA19078.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.763-476C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 7/10 | chr4 | 140460102 | ||||||
chr4:140460312
|
G | A | 1 | a0002c0002t0002g0233 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.763-686C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 7/10 | chr4 | 140460312 | ||||||
chr4:140460376
|
T | G | 76 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0002g0023others(73): Show | 80 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.763-750A>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 7/10 | chr4 | 140460376 | ||||||
chr4:140460450
|
T | C | 56 | a0002c0002t0001g0041a0002c0002t0003g0002a0002c0002t0003g0010others(53): Show | 59 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.763-824A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 7/10 | chr4 | 140460450 | ||||||
chr4:140460481
|
T | C | 108 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0001g0245others(105): Show | 112 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.763-855A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 7/10 | chr4 | 140460481 | ||||||
chr4:140460564
|
C | T | 2 | a0002c0002t0002g0234a0002c0002t0002g0235 | 2 | HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.763-938G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 7/10 | chr4 | 140460564 | ||||||
chr4:140460897
|
G | A | 4 | a0001c0001t0001g0224a0001c0001t0002g0119a0001c0001t0002g0132others(1): Show | 4 | HG02300.hp1 HG02622.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.762+1032C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 7/10 | chr4 | 140460897 | ||||||
chr4:140460923
|
A | G | 1 | a0001c0001t0001g0176 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.762+1006T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 7/10 | chr4 | 140460923 | ||||||
chr4:140460999
|
T | C | 8 | a0002c0002t0001g0041a0002c0002t0003g0014a0002c0002t0003g0016others(5): Show | 8 | NA18945.hp1 NA18948.hp2 NA18989.hp1 others(5): Show |
intron_variant | MODIFIER | c.762+930A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 7/10 | chr4 | 140460999 | ||||||
chr4:140461071
|
A | G | 76 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0002g0023others(73): Show | 80 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.762+858T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 7/10 | chr4 | 140461071 | ||||||
chr4:140461357
|
A | C | 17 | a0002c0002t0001g0067a0002c0002t0002g0023a0002c0002t0002g0072others(14): Show | 18 | HG00639.hp1 HG00738.hp2 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.762+572T>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 7/10 | chr4 | 140461357 | ||||||
chr4:140461460
|
T | C | 76 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0002g0023others(73): Show | 80 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.762+469A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 7/10 | chr4 | 140461460 | ||||||
chr4:140461809
|
AATT | A | 76 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0002g0023others(73): Show | 80 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.762+117_762+119del others(3): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 7/10 | chr4 | 140461809 | ||||||
chr4:140461880
|
T | TAC | 112 | a0001c0001t0001g0008a0001c0001t0001g0077a0001c0001t0001g0079others(109): Show | 113 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.762+47_762+48dupGT | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 7/10 | chr4 | 140461880 | ||||||
chr4:140461880
|
T | TACAC | 36 | a0001c0001t0001g0073a0001c0001t0001g0085a0001c0001t0001g0086others(33): Show | 36 | HG00408.hp1 HG00597.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.762+45_762+48dupGT others(2): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 7/10 | chr4 | 140461880 | ||||||
chr4:140461880
|
T | TACACAC | 6 | a0001c0001t0001g0065a0001c0001t0001g0312a0001c0001t0001g0313others(3): Show | 6 | HG02451.hp1 HG03486.hp2 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.762+43_762+48dupGT others(4): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 7/10 | chr4 | 140461880 | ||||||
chr4:140461880
|
TAC | T | 24 | a0001c0001t0001g0122a0001c0001t0001g0131a0001c0001t0001g0156others(21): Show | 24 | HG00738.hp1 HG01192.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.762+47_762+48delGT | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 7/10 | chr4 | 140461880 | ||||||
chr4:140461880
|
TACAC | T | 58 | a0001c0001t0001g0135a0001c0001t0001g0194a0001c0001t0001g0200others(55): Show | 61 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.762+45_762+48delGT others(2): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 7/10 | chr4 | 140461880 | ||||||
chr4:140461880
|
TACACACA others(3): Show |
T | 3 | a0002c0005t0001g0083a0002c0005t0003g0082a0002c0005t0004g0081 | 3 | HG02040.hp1 NA18939.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.762+39_762+48delGT others(8): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 7/10 | chr4 | 140461880 | ||||||
chr4:140462218
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.687-214G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 6/10 | chr4 | 140462218 | ||||||
chr4:140462417
|
A | C | 1 | a0002c0002t0002g0269 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.687-413T>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 6/10 | chr4 | 140462417 | ||||||
chr4:140462805
|
G | T | 3 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0134 | 3 | HG02818.hp2 HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.687-801C>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 6/10 | chr4 | 140462805 | ||||||
chr4:140462890
|
AC | A | 3 | a0002c0002t0004g0003a0002c0002t0004g0056a0002c0002t0004g0058 | 4 | HG01192.hp2 HG02486.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.687-887delG | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 6/10 | chr4 | 140462890 | ||||||
chr4:140462892
|
G | A | 3 | a0002c0002t0004g0003a0002c0002t0004g0056a0002c0002t0004g0058 | 4 | HG01192.hp2 HG02486.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.687-888C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 6/10 | chr4 | 140462892 | ||||||
chr4:140463053
|
C | T | 56 | a0002c0002t0001g0041a0002c0002t0002g0023a0002c0002t0003g0002others(53): Show | 59 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.687-1049G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 6/10 | chr4 | 140463053 | ||||||
chr4:140463149
|
A | C | 1 | a0002c0002t0002g0078 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.687-1145T>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 6/10 | chr4 | 140463149 | ||||||
chr4:140463406
|
C | T | 1 | a0002c0002t0002g0269 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.687-1402G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 6/10 | chr4 | 140463406 | ||||||
chr4:140463432
|
T | A | 32 | a0002c0002t0001g0245a0002c0002t0001g0276a0002c0002t0001g0279others(29): Show | 32 | HG00544.hp1 HG00609.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.687-1428A>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 6/10 | chr4 | 140463432 | ||||||
chr4:140463621
|
T | C | 108 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0001g0245others(105): Show | 112 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.686+1275A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 6/10 | chr4 | 140463621 | ||||||
chr4:140464111
|
G | A | 1 | a0001c0001t0001g0176 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.686+785C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 6/10 | chr4 | 140464111 | ||||||
chr4:140464130
|
C | A | 76 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0002g0023others(73): Show | 80 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.686+766G>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 6/10 | chr4 | 140464130 | ||||||
chr4:140464301
|
C | T | 73 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0002g0023others(70): Show | 77 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.686+595G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 6/10 | chr4 | 140464301 | ||||||
chr4:140464387
|
A | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0131 | 3 | HG01243.hp1 HG01496.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.686+509T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 6/10 | chr4 | 140464387 | ||||||
chr4:140464493
|
T | A | 76 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0002g0023others(73): Show | 80 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.686+403A>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 6/10 | chr4 | 140464493 | ||||||
chr4:140464517
|
C | G | 76 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0002g0023others(73): Show | 80 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.686+379G>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 6/10 | chr4 | 140464517 | ||||||
chr4:140465171
|
T | C | 1 | a0001c0001t0001g0299 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.573-162A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140465171 | ||||||
chr4:140465701
|
T | C | 1 | a0002c0002t0002g0267 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.573-692A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140465701 | ||||||
chr4:140465709
|
G | A | 1 | a0001c0001t0004g0275 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.573-700C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140465709 | ||||||
chr4:140466161
|
CAGA | C | 76 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0002g0023others(73): Show | 80 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.573-1155_573-1153d others(5): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140466161 | ||||||
chr4:140466168
|
T | C | 2 | a0001c0001t0001g0183a0001c0001t0001g0187 | 2 | NA19078.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.573-1159A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140466168 | ||||||
chr4:140466196
|
C | T | 76 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0002g0023others(73): Show | 80 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.573-1187G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140466196 | ||||||
chr4:140466284
|
C | T | 108 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0001g0245others(105): Show | 112 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.573-1275G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140466284 | ||||||
chr4:140466711
|
T | A | 1 | a0001c0001t0002g0292 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.573-1702A>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140466711 | ||||||
chr4:140466865
|
T | C | 3 | a0002c0005t0001g0083a0002c0005t0003g0082a0002c0005t0004g0081 | 3 | HG02040.hp1 NA18939.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.573-1856A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140466865 | ||||||
chr4:140466875
|
A | G | 76 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0002g0023others(73): Show | 80 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.573-1866T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140466875 | ||||||
chr4:140467088
|
T | A | 1 | a0002c0002t0002g0272 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.573-2079A>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140467088 | ||||||
chr4:140467094
|
A | G | 76 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0002g0023others(73): Show | 80 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.573-2085T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140467094 | ||||||
chr4:140467163
|
C | T | 57 | a0002c0002t0001g0041a0002c0002t0002g0023a0002c0002t0003g0002others(54): Show | 60 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.573-2154G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140467163 | ||||||
chr4:140467243
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.573-2234A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140467243 | ||||||
chr4:140467246
|
C | T | 1 | a0001c0001t0001g0008 | 2 | NA18970.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.573-2237G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140467246 | ||||||
chr4:140467289
|
G | T | 76 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0002g0023others(73): Show | 80 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.573-2280C>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140467289 | ||||||
chr4:140467360
|
G | A | 37 | a0001c0001t0001g0287a0001c0001t0001g0299a0001c0001t0001g0303others(34): Show | 38 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.573-2351C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140467360 | ||||||
chr4:140467494
|
A | C | 1 | a0002c0002t0004g0059 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.573-2485T>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140467494 | ||||||
chr4:140467495
|
C | A | 76 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0002g0023others(73): Show | 80 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.573-2486G>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140467495 | ||||||
chr4:140467665
|
A | C | 1 | a0001c0001t0001g0188 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.573-2656T>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140467665 | ||||||
chr4:140467778
|
A | G | 3 | a0002c0005t0001g0083a0002c0005t0003g0082a0002c0005t0004g0081 | 3 | HG02040.hp1 NA18939.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.573-2769T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140467778 | ||||||
chr4:140467821
|
T | C | 76 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0002g0023others(73): Show | 80 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.573-2812A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140467821 | ||||||
chr4:140468052
|
ACTATTAA others(6): Show |
A | 1 | a0002c0002t0003g0016 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.573-3056_573-3044d others(15): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140468052 | ||||||
chr4:140468053
|
CTATTAAA others(1): Show |
C | 72 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0002g0023others(69): Show | 76 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.573-3052_573-3045d others(10): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140468053 | ||||||
chr4:140468054
|
TATTAA | T | 3 | a0002c0005t0001g0083a0002c0005t0003g0082a0002c0005t0004g0081 | 3 | HG02040.hp1 NA18939.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.573-3050_573-3046d others(7): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140468054 | ||||||
chr4:140468071
|
A | C | 1 | a0002c0002t0003g0016 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.573-3062T>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140468071 | ||||||
chr4:140468123
|
CTATTA | C | 76 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0002g0023others(73): Show | 80 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.573-3119_573-3115d others(7): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140468123 | ||||||
chr4:140468285
|
A | G | 3 | a0002c0005t0001g0083a0002c0005t0003g0082a0002c0005t0004g0081 | 3 | HG02040.hp1 NA18939.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.573-3276T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140468285 | ||||||
chr4:140468461
|
T | A | 73 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0002g0023others(70): Show | 77 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.572+3314A>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140468461 | ||||||
chr4:140468704
|
C | G | 108 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0001g0245others(105): Show | 112 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.572+3071G>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140468704 | ||||||
chr4:140468956
|
A | G | 76 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0002g0023others(73): Show | 80 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.572+2819T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140468956 | ||||||
chr4:140469035
|
A | G | 1 | a0001c0001t0001g0164 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.572+2740T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140469035 | ||||||
chr4:140469950
|
C | CG | 4 | a0001c0001t0001g0161a0001c0001t0002g0315a0002c0002t0003g0032others(1): Show | 4 | HG00544.hp2 HG02071.hp1 HG02074.hp1 others(1): Show |
intron_variant | MODIFIER | c.572+1824dupC | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140469950 | ||||||
chr4:140470007
|
C | A | 3 | a0002c0005t0001g0083a0002c0005t0003g0082a0002c0005t0004g0081 | 3 | HG02040.hp1 NA18939.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.572+1768G>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140470007 | ||||||
chr4:140470025
|
C | G | 51 | a0001c0001t0002g0223a0002c0002t0001g0041a0002c0002t0002g0023others(48): Show | 53 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.572+1750G>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140470025 | ||||||
chr4:140470216
|
A | G | 1 | a0001c0001t0011g0320 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.572+1559T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140470216 | ||||||
chr4:140470245
|
G | A | 1 | a0001c0001t0002g0271 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.572+1530C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140470245 | ||||||
chr4:140470403
|
G | A | 65 | a0001c0001t0001g0065a0001c0001t0005g0076a0001c0007t0004g0064others(62): Show | 68 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.572+1372C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140470403 | ||||||
chr4:140470420
|
A | G | 3 | a0002c0002t0003g0011a0002c0002t0003g0034a0002c0002t0003g0036 | 3 | NA18975.hp2 NA18992.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.572+1355T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140470420 | ||||||
chr4:140470459
|
T | C | 6 | a0001c0001t0002g0009a0001c0001t0002g0290a0001c0001t0002g0291others(3): Show | 7 | HG00609.hp2 HG00673.hp1 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.572+1316A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140470459 | ||||||
chr4:140470482
|
C | T | 1 | a0002c0002t0003g0007 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.572+1293G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140470482 | ||||||
chr4:140470544
|
G | T | 149 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0261others(146): Show | 154 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.572+1231C>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140470544 | ||||||
chr4:140470582
|
C | A | 50 | a0002c0002t0001g0041a0002c0002t0002g0023a0002c0002t0003g0002others(47): Show | 52 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.572+1193G>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140470582 | ||||||
chr4:140470673
|
C | A | 106 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0287others(103): Show | 111 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.572+1102G>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140470673 | ||||||
chr4:140470714
|
T | G | 43 | a0001c0001t0001g0261a0001c0001t0002g0271a0001c0001t0004g0275others(40): Show | 43 | HG00544.hp1 HG00609.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.572+1061A>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140470714 | ||||||
chr4:140470884
|
A | T | 1 | a0002c0002t0003g0043 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.572+891T>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140470884 | ||||||
chr4:140470887
|
A | AT | 10 | a0001c0001t0001g0160a0001c0001t0001g0303a0001c0001t0001g0310others(7): Show | 10 | HG00408.hp1 HG01106.hp2 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.572+887dupA | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140470887 | ||||||
chr4:140470887
|
A | ATT | 110 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0287others(107): Show | 115 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.572+886_572+887dup others(2): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140470887 | ||||||
chr4:140470887
|
A | ATTT | 31 | a0001c0001t0001g0261a0002c0002t0001g0245a0002c0002t0001g0276others(28): Show | 31 | HG00544.hp1 HG00642.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.572+885_572+887dup others(3): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140470887 | ||||||
chr4:140471072
|
A | G | 8 | a0002c0002t0003g0025a0002c0002t0003g0030a0002c0002t0003g0035others(5): Show | 8 | HG00408.hp2 HG02523.hp2 NA18954.hp2 others(5): Show |
intron_variant | MODIFIER | c.572+703T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140471072 | ||||||
chr4:140471121
|
G | A | 43 | a0001c0001t0001g0261a0001c0001t0002g0271a0001c0001t0004g0275others(40): Show | 43 | HG00544.hp1 HG00609.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.572+654C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140471121 | ||||||
chr4:140471176
|
G | A | 106 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0287others(103): Show | 111 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.572+599C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140471176 | ||||||
chr4:140471227
|
T | TTTCC | 35 | a0001c0001t0001g0088a0001c0001t0001g0099a0001c0001t0001g0101others(32): Show | 35 | HG00280.hp1 HG00597.hp1 HG01123.hp1 others(32): Show |
intron_variant | MODIFIER | c.572+544_572+547dup others(4): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140471227 | ||||||
chr4:140471227
|
T | TTTCCTTC others(1): Show |
16 | a0001c0001t0001g0073a0001c0001t0001g0153a0001c0001t0001g0174others(13): Show | 16 | HG01070.hp2 HG01175.hp2 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.572+540_572+547dup others(8): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140471227 | ||||||
chr4:140471227
|
T | TTTCCTTC others(5): Show |
7 | a0001c0001t0001g0084a0001c0001t0001g0087a0001c0001t0001g0182others(4): Show | 7 | HG00323.hp2 HG01261.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.572+536_572+547dup others(12): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140471227 | ||||||
chr4:140471227
|
T | TTTCCTTC others(9): Show |
1 | a0001c0001t0001g0172 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.572+532_572+547dup others(16): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140471227 | ||||||
chr4:140471227
|
TTTCC | T | 47 | a0001c0001t0001g0079a0001c0001t0001g0086a0001c0001t0001g0094others(44): Show | 48 | HG00140.hp2 HG00544.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.572+544_572+547del others(4): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140471227 | ||||||
chr4:140471227
|
TTTCCTTC others(1): Show |
T | 28 | a0001c0001t0001g0146a0001c0001t0001g0287a0001c0001t0001g0303others(25): Show | 29 | HG00408.hp1 HG00544.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.572+540_572+547del others(8): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140471227 | ||||||
chr4:140471227
|
TTTCCTTC others(5): Show |
T | 17 | a0001c0001t0001g0147a0001c0001t0001g0207a0001c0001t0001g0295others(14): Show | 18 | HG01106.hp2 HG01884.hp1 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.572+536_572+547del others(12): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140471227 | ||||||
chr4:140471227
|
TTTCCTTC others(9): Show |
T | 17 | a0001c0001t0005g0239a0001c0001t0005g0240a0001c0001t0005g0241others(14): Show | 17 | HG00639.hp1 HG01074.hp1 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.572+532_572+547del others(16): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140471227 | ||||||
chr4:140471227
|
TTTCCTTC others(13): Show |
T | 47 | a0001c0001t0001g0008a0001c0001t0004g0294a0002c0002t0001g0041others(44): Show | 51 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.572+528_572+547del others(20): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140471227 | ||||||
chr4:140471227
|
TTTCCTTC others(17): Show |
T | 4 | a0001c0001t0001g0065a0001c0001t0005g0076a0002c0002t0004g0069others(1): Show | 4 | HG02258.hp2 HG02451.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.572+524_572+547del others(24): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140471227 | ||||||
chr4:140471227
|
TTTCCTTC others(21): Show |
T | 3 | a0001c0007t0004g0064a0002c0002t0001g0067a0002c0002t0002g0072 | 3 | HG02559.hp2 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.572+520_572+547del others(28): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140471227 | ||||||
chr4:140471227
|
TTTCCTTC others(25): Show |
T | 2 | a0002c0002t0004g0068a0002c0002t0004g0071 | 2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.572+516_572+547del others(32): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140471227 | ||||||
chr4:140471395
|
T | G | 1 | a0001c0001t0001g0200 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.572+380A>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140471395 | ||||||
chr4:140471408
|
C | T | 3 | a0002c0005t0001g0083a0002c0005t0003g0082a0002c0005t0004g0081 | 3 | HG02040.hp1 NA18939.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.572+367G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140471408 | ||||||
chr4:140471678
|
T | A | 2 | a0001c0001t0001g0206a0001c0001t0001g0215 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.572+97A>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 5/10 | chr4 | 140471678 | ||||||
chr4:140471878
|
A | G | 1 | a0001c0001t0002g0063 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.526-57T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 4/10 | chr4 | 140471878 | ||||||
chr4:140472017
|
A | G | 2 | a0002c0002t0004g0069a0002c0002t0004g0070 | 2 | HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.526-196T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 4/10 | chr4 | 140472017 | ||||||
chr4:140472031
|
C | G | 1 | a0002c0002t0004g0055 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.526-210G>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 4/10 | chr4 | 140472031 | ||||||
chr4:140472119
|
A | G | 1 | a0002c0002t0003g0033 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.526-298T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 4/10 | chr4 | 140472119 | ||||||
chr4:140472212
|
G | C | 2 | a0001c0001t0001g0321a0001c0001t0001g0322 | 2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.526-391C>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 4/10 | chr4 | 140472212 | ||||||
chr4:140472384
|
C | T | 5 | a0001c0001t0005g0239a0001c0001t0005g0240a0001c0001t0005g0241others(2): Show | 5 | HG02647.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.526-563G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 4/10 | chr4 | 140472384 | ||||||
chr4:140472516
|
GA | G | 59 | a0001c0001t0001g0065a0001c0001t0005g0076a0001c0007t0004g0064others(56): Show | 62 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.526-696delT | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 4/10 | chr4 | 140472516 | ||||||
chr4:140472570
|
T | A | 149 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0261others(146): Show | 154 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.526-749A>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 4/10 | chr4 | 140472570 | ||||||
chr4:140472681
|
A | G | 1 | a0001c0001t0002g0315 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.526-860T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 4/10 | chr4 | 140472681 | ||||||
chr4:140472685
|
C | T | 1 | a0002c0002t0003g0035 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.526-864G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 4/10 | chr4 | 140472685 | ||||||
chr4:140472843
|
A | G | 149 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0261others(146): Show | 154 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.526-1022T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 4/10 | chr4 | 140472843 | ||||||
chr4:140473063
|
G | A | 149 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0261others(146): Show | 154 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.526-1242C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 4/10 | chr4 | 140473063 | ||||||
chr4:140473300
|
T | C | 149 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0261others(146): Show | 154 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.526-1479A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 4/10 | chr4 | 140473300 | ||||||
chr4:140473302
|
G | A | 43 | a0001c0001t0001g0261a0001c0001t0002g0271a0001c0001t0004g0275others(40): Show | 43 | HG00544.hp1 HG00609.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.526-1481C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 4/10 | chr4 | 140473302 | ||||||
chr4:140473391
|
A | T | 1 | a0001c0001t0001g0210 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.525+1422T>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 4/10 | chr4 | 140473391 | ||||||
chr4:140473564
|
G | A | 149 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0261others(146): Show | 154 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.525+1249C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 4/10 | chr4 | 140473564 | ||||||
chr4:140473851
|
A | G | 36 | a0001c0001t0001g0008a0001c0001t0001g0287a0001c0001t0001g0295others(33): Show | 38 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.525+962T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 4/10 | chr4 | 140473851 | ||||||
chr4:140473865
|
A | T | 149 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0261others(146): Show | 154 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.525+948T>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 4/10 | chr4 | 140473865 | ||||||
chr4:140473868
|
A | AT | 105 | a0001c0001t0001g0077a0001c0001t0001g0079a0001c0001t0001g0084others(102): Show | 105 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.525+944dupA | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 4/10 | chr4 | 140473868 | ||||||
chr4:140473868
|
AT | A | 32 | a0001c0001t0001g0261a0002c0002t0001g0245a0002c0002t0001g0276others(29): Show | 32 | HG00609.hp1 HG00642.hp2 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.525+944delA | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 4/10 | chr4 | 140473868 | ||||||
chr4:140474150
|
C | T | 7 | a0001c0001t0001g0006a0001c0001t0001g0073a0001c0001t0001g0131others(4): Show | 10 | HG01243.hp1 HG01496.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.525+663G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 4/10 | chr4 | 140474150 | ||||||
chr4:140474471
|
C | T | 5 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0002g0126others(2): Show | 5 | HG02280.hp2 HG03486.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+342G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 4/10 | chr4 | 140474471 | ||||||
chr4:140474683
|
G | A | 106 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0287others(103): Show | 111 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.525+130C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 4/10 | chr4 | 140474683 | ||||||
chr4:140474803
|
G | C | 1 | a0001c0001t0002g0271 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.525+10C>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 4/10 | chr4 | 140474803 | ||||||
chr4:140474808
|
C | T | 1 | a0001c0001t0001g0217 | 1 | NA19057.hp2 | splice_region_variant&intron_variant | LOW | c.525+5G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 4/10 | chr4 | 140474808 | ||||||
chr4:140474812
|
C | T | 1 | a0002c0002t0012g0249 | 1 | HG02155.hp1 | splice_donor_variant&intron_variant | HIGH | c.525+1G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 4/10 | chr4 | 140474812 | ||||||
chr4:140474975
|
T | C | 1 | a0002c0002t0003g0018 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.392-29A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140474975 | ||||||
chr4:140475045
|
C | T | 1 | a0002c0002t0002g0023 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.392-99G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140475045 | ||||||
chr4:140475353
|
G | A | 1 | a0002c0002t0001g0067 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.392-407C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140475353 | ||||||
chr4:140475660
|
C | CA | 11 | a0001c0001t0001g0103a0001c0001t0001g0110a0001c0001t0001g0111others(8): Show | 11 | HG00140.hp1 HG01192.hp1 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.392-715dupT | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140475660 | ||||||
chr4:140475660
|
C | CAAA | 32 | a0001c0001t0001g0008a0001c0001t0001g0287a0001c0001t0001g0299others(29): Show | 34 | HG00408.hp1 HG00597.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.392-717_392-715dup others(3): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140475660 | ||||||
chr4:140475660
|
C | CAAAA | 54 | a0001c0001t0001g0295a0001c0001t0001g0305a0001c0001t0001g0314others(51): Show | 57 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.392-718_392-715dup others(4): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140475660 | ||||||
chr4:140475660
|
C | CAAAAA | 43 | a0001c0001t0001g0065a0001c0001t0004g0275a0001c0001t0005g0066others(40): Show | 43 | HG00609.hp1 HG00642.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.392-719_392-715dup others(5): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140475660 | ||||||
chr4:140475660
|
C | CAAAAAA | 16 | a0001c0001t0001g0261a0001c0001t0005g0242a0001c0001t0005g0243others(13): Show | 16 | HG00544.hp1 HG01175.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.392-720_392-715dup others(6): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140475660 | ||||||
chr4:140475726
|
C | T | 1 | a0001c0001t0005g0076 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.392-780G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140475726 | ||||||
chr4:140475807
|
C | CT | 12 | a0001c0001t0001g0160a0001c0001t0001g0174a0001c0001t0001g0188others(9): Show | 12 | HG01175.hp2 HG01978.hp2 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.392-862dupA | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140475807 | ||||||
chr4:140475807
|
CT | C | 66 | a0001c0001t0001g0095a0001c0001t0001g0146a0001c0001t0001g0147others(63): Show | 69 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.392-862delA | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140475807 | ||||||
chr4:140475807
|
CTT | C | 42 | a0001c0001t0001g0008a0001c0001t0001g0287a0001c0001t0001g0295others(39): Show | 44 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.392-863_392-862del others(2): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140475807 | ||||||
chr4:140475807
|
CTTT | C | 39 | a0001c0001t0001g0261a0001c0001t0002g0271a0001c0001t0005g0066others(36): Show | 39 | HG00544.hp1 HG00609.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.392-864_392-862del others(3): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140475807 | ||||||
chr4:140475812
|
T | C | 1 | a0002c0002t0003g0043 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.392-866A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140475812 | ||||||
chr4:140475814
|
T | C | 1 | a0002c0002t0004g0055 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.392-868A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140475814 | ||||||
chr4:140475867
|
A | G | 43 | a0001c0001t0001g0261a0001c0001t0002g0271a0001c0001t0004g0275others(40): Show | 43 | HG00544.hp1 HG00609.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.392-921T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140475867 | ||||||
chr4:140476074
|
A | C | 1 | a0001c0001t0001g0314 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.392-1128T>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140476074 | ||||||
chr4:140476186
|
A | G | 149 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0261others(146): Show | 154 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.392-1240T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140476186 | ||||||
chr4:140476231
|
A | G | 1 | a0002c0002t0001g0067 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.392-1285T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140476231 | ||||||
chr4:140476499
|
T | A | 1 | a0001c0001t0001g0314 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.392-1553A>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140476499 | ||||||
chr4:140476506
|
A | G | 1 | a0001c0001t0004g0136 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.392-1560T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140476506 | ||||||
chr4:140476638
|
C | T | 2 | a0002c0002t0002g0231a0002c0002t0002g0232 | 2 | HG01255.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.392-1692G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140476638 | ||||||
chr4:140476792
|
T | A | 1 | a0001c0001t0002g0133 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.392-1846A>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140476792 | ||||||
chr4:140476804
|
C | A | 41 | a0001c0001t0001g0008a0001c0001t0001g0287a0001c0001t0001g0295others(38): Show | 43 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.392-1858G>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140476804 | ||||||
chr4:140477020
|
G | A | 25 | a0001c0001t0001g0006a0001c0001t0001g0073a0001c0001t0001g0089others(22): Show | 28 | HG00738.hp1 HG01169.hp2 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.392-2074C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140477020 | ||||||
chr4:140477077
|
A | G | 43 | a0001c0001t0001g0261a0001c0001t0002g0271a0001c0001t0004g0275others(40): Show | 43 | HG00544.hp1 HG00609.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.392-2131T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140477077 | ||||||
chr4:140477079
|
A | T | 322 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0065others(319): Show | 331 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.392-2133T>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140477079 | ||||||
chr4:140477087
|
C | A | 1 | a0001c0001t0003g0080 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.392-2141G>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140477087 | ||||||
chr4:140477152
|
G | C | 1 | a0002c0002t0001g0279 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.392-2206C>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140477152 | ||||||
chr4:140477698
|
T | C | 1 | a0001c0001t0001g0209 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.391+1792A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140477698 | ||||||
chr4:140477803
|
C | T | 43 | a0001c0001t0001g0261a0001c0001t0002g0271a0001c0001t0004g0275others(40): Show | 43 | HG00544.hp1 HG00609.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.391+1687G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140477803 | ||||||
chr4:140478274
|
C | T | 33 | a0001c0001t0001g0261a0002c0002t0001g0245a0002c0002t0001g0276others(30): Show | 33 | HG00544.hp1 HG00609.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.391+1216G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140478274 | ||||||
chr4:140478320
|
A | G | 1 | a0001c0001t0011g0320 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.391+1170T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140478320 | ||||||
chr4:140478455
|
T | C | 9 | a0001c0001t0001g0088a0001c0001t0001g0111a0001c0001t0001g0112others(6): Show | 9 | HG01884.hp1 HG02630.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.391+1035A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140478455 | ||||||
chr4:140478525
|
A | T | 1 | a0002c0002t0009g0228 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.391+965T>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140478525 | ||||||
chr4:140478763
|
CT | C | 149 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0146others(146): Show | 154 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.391+726delA | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140478763 | ||||||
chr4:140478891
|
G | A | 1 | a0001c0001t0002g0271 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.391+599C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140478891 | ||||||
chr4:140478912
|
A | G | 106 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0287others(103): Show | 111 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.391+578T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140478912 | ||||||
chr4:140478993
|
A | G | 2 | a0001c0001t0003g0080a0001c0001t0005g0117 | 2 | HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.391+497T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140478993 | ||||||
chr4:140479377
|
C | T | 41 | a0001c0001t0001g0008a0001c0001t0001g0287a0001c0001t0001g0295others(38): Show | 43 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.391+113G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140479377 | ||||||
chr4:140479413
|
T | A | 106 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0287others(103): Show | 111 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.391+77A>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140479413 | ||||||
chr4:140479416
|
A | G | 149 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0261others(146): Show | 154 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.391+74T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 3/10 | chr4 | 140479416 | ||||||
chr4:140479634
|
G | GA | 93 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0261others(90): Show | 95 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(92): Show |
splice_region_variant&intron_variant | LOW | c.254-8dupT | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140479634 | ||||||
chr4:140479730
|
G | A | 149 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0261others(146): Show | 154 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.254-103C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140479730 | ||||||
chr4:140479763
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.254-136C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140479763 | ||||||
chr4:140480001
|
T | G | 15 | a0001c0001t0001g0077a0001c0001t0001g0137a0001c0001t0001g0168others(12): Show | 15 | HG01358.hp2 HG02004.hp2 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.254-374A>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140480001 | ||||||
chr4:140480072
|
G | A | 149 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0261others(146): Show | 154 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.254-445C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140480072 | ||||||
chr4:140480135
|
A | T | 12 | a0001c0001t0001g0303a0001c0001t0001g0304a0001c0001t0001g0305others(9): Show | 12 | HG02155.hp2 NA18960.hp2 NA18979.hp2 others(9): Show |
intron_variant | MODIFIER | c.254-508T>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140480135 | ||||||
chr4:140480283
|
A | G | 149 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0261others(146): Show | 154 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.254-656T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140480283 | ||||||
chr4:140480342
|
G | C | 43 | a0001c0001t0001g0261a0001c0001t0002g0271a0001c0001t0004g0275others(40): Show | 43 | HG00544.hp1 HG00609.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.254-715C>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140480342 | ||||||
chr4:140480381
|
T | A | 3 | a0002c0002t0002g0230a0002c0002t0002g0231a0002c0002t0002g0232 | 3 | HG00738.hp2 HG01255.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.254-754A>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140480381 | ||||||
chr4:140480428
|
A | C | 1 | a0002c0005t0003g0082 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.254-801T>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140480428 | ||||||
chr4:140480508
|
T | C | 1 | a0001c0001t0001g0221 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.254-881A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140480508 | ||||||
chr4:140480702
|
G | A | 149 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0261others(146): Show | 154 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.254-1075C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140480702 | ||||||
chr4:140480727
|
AAACACAC others(4): Show |
A | 2 | a0001c0001t0002g0171a0002c0002t0002g0264 | 2 | HG04228.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.254-1111_254-1101d others(13): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140480727 | ||||||
chr4:140480727
|
AAACACAC others(6): Show |
A | 1 | a0001c0001t0001g0199 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.254-1113_254-1101d others(15): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140480727 | ||||||
chr4:140480728
|
AAC | A | 4 | a0001c0001t0001g0139a0001c0001t0001g0198a0001c0001t0001g0202others(1): Show | 4 | HG00639.hp2 HG02615.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.254-1103_254-1102d others(4): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140480728 | ||||||
chr4:140480728
|
AACAC | A | 10 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0001g0149others(7): Show | 10 | HG02040.hp1 HG02897.hp2 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.254-1105_254-1102d others(6): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140480728 | ||||||
chr4:140480728
|
AACACAC | A | 27 | a0001c0001t0001g0100a0001c0001t0001g0138a0001c0001t0001g0150others(24): Show | 28 | HG00438.hp2 HG00741.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.254-1107_254-1102d others(8): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140480728 | ||||||
chr4:140480728
|
AACACACA others(1): Show |
A | 67 | a0001c0001t0001g0077a0001c0001t0001g0079a0001c0001t0001g0084others(64): Show | 67 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.254-1109_254-1102d others(10): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140480728 | ||||||
chr4:140480728
|
AACACACA others(3): Show |
A | 33 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(30): Show | 33 | HG00642.hp2 HG00738.hp1 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.254-1111_254-1102d others(12): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140480728 | ||||||
chr4:140480728
|
AACACACA others(5): Show |
A | 74 | a0001c0001t0001g0073a0001c0001t0001g0089a0001c0001t0001g0173others(71): Show | 74 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.254-1113_254-1102d others(14): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140480728 | ||||||
chr4:140480728
|
AACACACA others(7): Show |
A | 22 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0131others(19): Show | 27 | HG00597.hp2 HG00609.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.254-1115_254-1102d others(16): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140480728 | ||||||
chr4:140480728
|
AACACACA others(9): Show |
A | 10 | a0001c0001t0001g0319a0001c0001t0002g0108a0001c0001t0002g0109others(7): Show | 10 | HG00280.hp2 HG01928.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.254-1117_254-1102d others(18): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140480728 | ||||||
chr4:140480728
|
AACACACA others(11): Show |
A | 56 | a0001c0001t0001g0065a0001c0001t0003g0080a0001c0001t0005g0117others(53): Show | 59 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.254-1119_254-1102d others(20): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140480728 | ||||||
chr4:140480728
|
AACACACA others(13): Show |
A | 2 | a0002c0002t0004g0055a0002c0002t0004g0057 | 2 | HG01884.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.254-1121_254-1102d others(22): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140480728 | ||||||
chr4:140480728
|
AACACACA others(15): Show |
A | 3 | a0001c0001t0001g0188a0001c0001t0001g0200a0001c0001t0001g0226 | 3 | HG01978.hp2 NA18948.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.254-1123_254-1102d others(24): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140480728 | ||||||
chr4:140480728
|
AACACACA others(19): Show |
A | 1 | a0001c0001t0005g0274 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.254-1127_254-1102d others(28): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140480728 | ||||||
chr4:140480810
|
C | T | 43 | a0001c0001t0001g0261a0001c0001t0002g0271a0001c0001t0004g0275others(40): Show | 43 | HG00544.hp1 HG00609.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.254-1183G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140480810 | ||||||
chr4:140480846
|
A | G | 149 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0261others(146): Show | 154 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.254-1219T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140480846 | ||||||
chr4:140480908
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.254-1281C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140480908 | ||||||
chr4:140481038
|
A | T | 106 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0287others(103): Show | 111 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.253+1289T>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140481038 | ||||||
chr4:140481041
|
C | A | 1 | a0001c0001t0001g0147 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.253+1286G>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140481041 | ||||||
chr4:140481049
|
C | T | 5 | a0001c0001t0002g0281a0001c0001t0002g0282a0001c0001t0002g0283others(2): Show | 5 | HG02258.hp1 HG02630.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.253+1278G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140481049 | ||||||
chr4:140481051
|
T | A | 1 | a0002c0002t0002g0230 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.253+1276A>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140481051 | ||||||
chr4:140481113
|
GC | G | 149 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0261others(146): Show | 154 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.253+1213delG | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140481113 | ||||||
chr4:140481120
|
C | G | 149 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0261others(146): Show | 154 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.253+1207G>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140481120 | ||||||
chr4:140481230
|
A | C | 149 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0261others(146): Show | 154 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.253+1097T>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140481230 | ||||||
chr4:140481231
|
G | A | 149 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0261others(146): Show | 154 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.253+1096C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140481231 | ||||||
chr4:140481304
|
A | T | 65 | a0001c0001t0001g0065a0001c0001t0005g0076a0001c0007t0004g0064others(62): Show | 68 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.253+1023T>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140481304 | ||||||
chr4:140481413
|
A | G | 149 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0261others(146): Show | 154 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.253+914T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140481413 | ||||||
chr4:140481430
|
A | C | 149 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0261others(146): Show | 154 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.253+897T>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140481430 | ||||||
chr4:140481455
|
C | A | 6 | a0002c0002t0001g0067a0002c0002t0002g0072a0002c0002t0004g0068others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.253+872G>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140481455 | ||||||
chr4:140481599
|
T | C | 1 | a0002c0002t0001g0067 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.253+728A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140481599 | ||||||
chr4:140481609
|
A | T | 1 | a0003c0003t0003g0044 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.253+718T>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140481609 | ||||||
chr4:140481745
|
T | C | 41 | a0001c0001t0001g0008a0001c0001t0001g0287a0001c0001t0001g0295others(38): Show | 43 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.253+582A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140481745 | ||||||
chr4:140481794
|
G | A | 1 | a0002c0002t0002g0269 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.253+533C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140481794 | ||||||
chr4:140482013
|
C | T | 1 | a0002c0002t0003g0032 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.253+314G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140482013 | ||||||
chr4:140482037
|
A | C | 1 | a0002c0002t0003g0060 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.253+290T>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140482037 | ||||||
chr4:140482079
|
T | C | 106 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0287others(103): Show | 111 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.253+248A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140482079 | ||||||
chr4:140482087
|
C | A | 149 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0261others(146): Show | 154 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.253+240G>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140482087 | ||||||
chr4:140482120
|
G | A | 106 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0287others(103): Show | 111 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.253+207C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 2/10 | chr4 | 140482120 | ||||||
chr4:140482562
|
A | G | 43 | a0001c0001t0001g0261a0001c0001t0002g0271a0001c0001t0004g0275others(40): Show | 43 | HG00544.hp1 HG00609.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.95-77T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140482562 | ||||||
chr4:140482648
|
C | T | 1 | a0001c0001t0001g0156 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.95-163G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140482648 | ||||||
chr4:140482845
|
C | A | 65 | a0001c0001t0001g0065a0001c0001t0005g0076a0001c0007t0004g0064others(62): Show | 68 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.95-360G>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140482845 | ||||||
chr4:140482894
|
C | T | 56 | a0002c0002t0001g0041a0002c0002t0002g0023a0002c0002t0003g0002others(53): Show | 59 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.95-409G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140482894 | ||||||
chr4:140482936
|
T | C | 1 | a0001c0001t0002g0318 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.95-451A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140482936 | ||||||
chr4:140483172
|
C | A | 322 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0065others(319): Show | 331 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.95-687G>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140483172 | ||||||
chr4:140483210
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.95-725T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140483210 | ||||||
chr4:140483235
|
G | A | 149 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0261others(146): Show | 154 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.95-750C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140483235 | ||||||
chr4:140483338
|
T | G | 1 | a0002c0002t0003g0043 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.95-853A>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140483338 | ||||||
chr4:140483468
|
T | C | 33 | a0001c0001t0001g0261a0002c0002t0001g0245a0002c0002t0001g0276others(30): Show | 33 | HG00544.hp1 HG00609.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.95-983A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140483468 | ||||||
chr4:140483644
|
A | C | 65 | a0001c0001t0001g0065a0001c0001t0005g0076a0001c0007t0004g0064others(62): Show | 68 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.95-1159T>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140483644 | ||||||
chr4:140483758
|
G | C | 105 | a0001c0001t0001g0065a0001c0001t0001g0287a0001c0001t0001g0295others(102): Show | 109 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.95-1273C>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140483758 | ||||||
chr4:140483758
|
G | T | 1 | a0001c0001t0001g0008 | 2 | NA18970.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.95-1273C>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140483758 | ||||||
chr4:140483820
|
C | T | 1 | a0002c0002t0002g0248 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.95-1335G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140483820 | ||||||
chr4:140483848
|
T | TA | 106 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0287others(103): Show | 111 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.95-1364dupT | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140483848 | ||||||
chr4:140483891
|
C | A | 4 | a0002c0002t0004g0068a0002c0002t0004g0069a0002c0002t0004g0070others(1): Show | 4 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-1406G>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140483891 | ||||||
chr4:140484261
|
A | G | 36 | a0001c0001t0001g0008a0001c0001t0001g0287a0001c0001t0001g0295others(33): Show | 38 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.95-1776T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140484261 | ||||||
chr4:140484364
|
T | G | 1 | a0004c0004t0002g0263 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.95-1879A>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140484364 | ||||||
chr4:140484397
|
A | G | 11 | a0001c0001t0001g0089a0001c0001t0001g0122a0001c0001t0002g0108others(8): Show | 11 | HG00738.hp1 HG01169.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.95-1912T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140484397 | ||||||
chr4:140484446
|
T | C | 149 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0261others(146): Show | 154 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.95-1961A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140484446 | ||||||
chr4:140484447
|
G | A | 106 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0287others(103): Show | 111 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.95-1962C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140484447 | ||||||
chr4:140484606
|
G | A | 1 | a0002c0002t0004g0055 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.95-2121C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140484606 | ||||||
chr4:140484652
|
T | A | 1 | a0001c0001t0001g0311 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.95-2167A>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140484652 | ||||||
chr4:140484705
|
GA | G | 4 | a0001c0001t0001g0224a0001c0001t0002g0119a0001c0001t0002g0132others(1): Show | 4 | HG02300.hp1 HG02622.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-2221delT | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140484705 | ||||||
chr4:140484779
|
C | G | 106 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0287others(103): Show | 111 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.95-2294G>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140484779 | ||||||
chr4:140484793
|
A | T | 1 | a0001c0001t0001g0100 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.95-2308T>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140484793 | ||||||
chr4:140484879
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.95-2394C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140484879 | ||||||
chr4:140484957
|
T | C | 41 | a0001c0001t0001g0008a0001c0001t0001g0287a0001c0001t0001g0295others(38): Show | 43 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.95-2472A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140484957 | ||||||
chr4:140484994
|
G | A | 1 | a0001c0001t0011g0320 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.95-2509C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140484994 | ||||||
chr4:140485102
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.95-2617C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140485102 | ||||||
chr4:140485114
|
C | A | 2 | a0001c0001t0001g0312a0001c0001t0001g0313 | 2 | NA18960.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.95-2629G>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140485114 | ||||||
chr4:140485144
|
A | T | 10 | a0001c0001t0002g0271a0001c0001t0004g0275a0001c0001t0005g0066others(7): Show | 10 | HG01106.hp2 HG02615.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.95-2659T>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140485144 | ||||||
chr4:140485505
|
A | G | 1 | a0002c0002t0002g0078 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.95-3020T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140485505 | ||||||
chr4:140485604
|
G | T | 43 | a0001c0001t0001g0261a0001c0001t0002g0271a0001c0001t0004g0275others(40): Show | 43 | HG00544.hp1 HG00609.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.95-3119C>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140485604 | ||||||
chr4:140485783
|
C | T | 1 | a0001c0001t0002g0132 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.95-3298G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140485783 | ||||||
chr4:140485803
|
C | A | 1 | a0001c0001t0004g0275 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.95-3318G>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140485803 | ||||||
chr4:140485810
|
T | TA | 8 | a0001c0001t0004g0127a0001c0001t0004g0128a0002c0002t0003g0013others(5): Show | 8 | HG01261.hp2 HG01978.hp1 HG02148.hp1 others(5): Show |
intron_variant | MODIFIER | c.95-3326dupT | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140485810 | ||||||
chr4:140485810
|
T | TAAAAAAA | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0002g0109others(3): Show | 6 | HG02040.hp1 HG03831.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.95-3332_95-3326dup others(7): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140485810 | ||||||
chr4:140485810
|
T | TAAAAAAA others(3): Show |
15 | a0001c0001t0001g0077a0001c0001t0001g0104a0001c0001t0001g0166others(12): Show | 15 | HG00280.hp1 HG01169.hp1 HG02004.hp2 others(12): Show |
intron_variant | MODIFIER | c.95-3335_95-3326dup others(10): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140485810 | ||||||
chr4:140485810
|
T | TAAAAAAA others(4): Show |
24 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0106others(21): Show | 24 | HG00323.hp2 HG00597.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.95-3336_95-3326dup others(11): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140485810 | ||||||
chr4:140485810
|
T | TAAAAAAA others(5): Show |
12 | a0001c0001t0001g0006a0001c0001t0001g0079a0001c0001t0001g0084others(9): Show | 13 | HG01074.hp2 HG01496.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.95-3337_95-3326dup others(12): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140485810 | ||||||
chr4:140485810
|
T | TAAAAAAA others(6): Show |
8 | a0001c0001t0001g0099a0001c0001t0001g0196a0001c0001t0001g0197others(5): Show | 8 | HG00639.hp2 HG02559.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.95-3338_95-3326dup others(13): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140485810 | ||||||
chr4:140485810
|
T | TAAAAAAA others(7): Show |
11 | a0001c0001t0001g0131a0001c0001t0001g0201a0001c0001t0001g0202others(8): Show | 11 | HG01243.hp1 HG01255.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.95-3339_95-3326dup others(14): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140485810 | ||||||
chr4:140485810
|
T | TAAAAAAA others(8): Show |
15 | a0001c0001t0001g0100a0001c0001t0001g0135a0001c0001t0001g0207others(12): Show | 15 | HG00741.hp1 HG00741.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.95-3340_95-3326dup others(15): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140485810 | ||||||
chr4:140485810
|
T | TAAAAAAA others(9): Show |
4 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218others(1): Show | 4 | HG01175.hp2 HG02132.hp1 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-3341_95-3326dup others(16): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140485810 | ||||||
chr4:140485810
|
T | TAAAAAAA others(10): Show |
3 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0002g0133 | 3 | HG02723.hp2 NA18980.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.95-3342_95-3326dup others(17): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140485810 | ||||||
chr4:140485810
|
T | TAAAAAAA others(11): Show |
1 | a0001c0001t0002g0063 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.95-3343_95-3326dup others(18): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140485810 | ||||||
chr4:140485810
|
T | TAAAAAAA others(13): Show |
1 | a0002c0002t0002g0235 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.95-3345_95-3326dup others(20): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140485810 | ||||||
chr4:140485810
|
TA | T | 5 | a0002c0002t0003g0045a0002c0002t0004g0003a0002c0002t0004g0058others(2): Show | 6 | HG01192.hp2 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.95-3326delT | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140485810 | ||||||
chr4:140485810
|
TAA | T | 24 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0161others(21): Show | 25 | HG00408.hp2 HG00438.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.95-3327_95-3326del others(2): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140485810 | ||||||
chr4:140485810
|
TAAA | T | 20 | a0001c0001t0001g0160a0001c0001t0004g0118a0002c0002t0002g0023others(17): Show | 20 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.95-3328_95-3326del others(3): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140485810 | ||||||
chr4:140485810
|
TAAAA | T | 10 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(7): Show | 10 | HG00438.hp2 HG02165.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.95-3329_95-3326del others(4): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140485810 | ||||||
chr4:140485810
|
TAAAAA | T | 10 | a0001c0001t0001g0150a0001c0001t0001g0152a0001c0001t0001g0153others(7): Show | 10 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.95-3330_95-3326del others(5): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140485810 | ||||||
chr4:140485810
|
TAAAAAA | T | 6 | a0001c0001t0001g0090a0001c0001t0002g0271a0001c0001t0002g0297others(3): Show | 6 | HG02109.hp1 HG02615.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-3331_95-3326del others(6): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140485810 | ||||||
chr4:140485810
|
TAAAAAAA | T | 14 | a0001c0001t0001g0295a0001c0001t0002g0296a0001c0001t0002g0316others(11): Show | 14 | HG00642.hp2 HG00673.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.95-3332_95-3326del others(7): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140485810 | ||||||
chr4:140485810
|
TAAAAAAA others(1): Show |
T | 61 | a0001c0001t0001g0008a0001c0001t0001g0149a0001c0001t0001g0261others(58): Show | 64 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.95-3333_95-3326del others(8): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140485810 | ||||||
chr4:140485810
|
TAAAAAAA others(2): Show |
T | 14 | a0001c0001t0001g0088a0001c0001t0001g0303a0001c0001t0002g0148others(11): Show | 14 | HG01255.hp2 HG01515.hp2 HG01993.hp2 others(11): Show |
intron_variant | MODIFIER | c.95-3334_95-3326del others(9): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140485810 | ||||||
chr4:140485810
|
TAAAAAAA others(3): Show |
T | 15 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0101others(12): Show | 15 | HG01123.hp1 HG01361.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.95-3335_95-3326del others(10): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140485810 | ||||||
chr4:140485810
|
TAAAAAAA others(4): Show |
T | 3 | a0001c0001t0001g0065a0001c0001t0001g0139a0001c0001t0003g0225 | 3 | HG02109.hp2 HG02451.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.95-3336_95-3326del others(11): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140485810 | ||||||
chr4:140485810
|
TAAAAAAA others(6): Show |
T | 5 | a0001c0001t0001g0138a0001c0001t0003g0080a0001c0001t0005g0116others(2): Show | 5 | HG02486.hp2 HG03139.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.95-3338_95-3326del others(13): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140485810 | ||||||
chr4:140485810
|
TAAAAAAA others(7): Show |
T | 3 | a0001c0001t0001g0073a0001c0001t0006g0004a0001c0001t0006g0005 | 5 | HG01891.hp1 HG02622.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-3339_95-3326del others(14): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140485810 | ||||||
chr4:140485810
|
TAAAAAAA others(8): Show |
T | 2 | a0001c0001t0002g0114a0001c0001t0002g0115 | 2 | HG01256.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.95-3340_95-3326del others(15): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140485810 | ||||||
chr4:140485810
|
TAAAAAAA others(9): Show |
T | 1 | a0001c0001t0002g0113 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.95-3341_95-3326del others(16): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140485810 | ||||||
chr4:140485810
|
TAAAAAAA others(10): Show |
T | 1 | a0001c0001t0001g0137 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.95-3342_95-3326del others(17): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140485810 | ||||||
chr4:140485810
|
TAAAAAAA others(11): Show |
T | 1 | a0001c0001t0004g0136 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.95-3343_95-3326del others(18): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140485810 | ||||||
chr4:140485810
|
TAAAAAAA others(13): Show |
T | 1 | a0001c0001t0001g0085 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.95-3345_95-3326del others(20): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140485810 | ||||||
chr4:140486002
|
A | G | 106 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0287others(103): Show | 111 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.95-3517T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140486002 | ||||||
chr4:140486025
|
T | C | 1 | a0002c0002t0004g0071 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.95-3540A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140486025 | ||||||
chr4:140486068
|
G | T | 43 | a0001c0001t0001g0261a0001c0001t0002g0271a0001c0001t0004g0275others(40): Show | 43 | HG00544.hp1 HG00609.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.95-3583C>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140486068 | ||||||
chr4:140486273
|
T | TCA | 43 | a0001c0001t0001g0261a0001c0001t0002g0271a0001c0001t0004g0275others(40): Show | 43 | HG00544.hp1 HG00609.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.95-3789_95-3788ins others(2): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140486273 | ||||||
chr4:140486273
|
T | TCC | 106 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0287others(103): Show | 111 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.95-3789_95-3788ins others(2): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140486273 | ||||||
chr4:140486356
|
T | C | 1 | a0001c0001t0001g0224 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.95-3871A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140486356 | ||||||
chr4:140486913
|
G | T | 1 | a0001c0001t0001g0135 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.95-4428C>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140486913 | ||||||
chr4:140487063
|
T | C | 1 | a0001c0001t0005g0076 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.95-4578A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140487063 | ||||||
chr4:140487173
|
T | C | 6 | a0002c0002t0001g0067a0002c0002t0002g0072a0002c0002t0004g0068others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-4688A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140487173 | ||||||
chr4:140487471
|
T | G | 1 | a0001c0001t0001g0110 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.95-4986A>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140487471 | ||||||
chr4:140487765
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.95-5280A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140487765 | ||||||
chr4:140487910
|
G | A | 106 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0287others(103): Show | 111 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.95-5425C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140487910 | ||||||
chr4:140488151
|
C | G | 65 | a0001c0001t0001g0065a0001c0001t0005g0076a0001c0007t0004g0064others(62): Show | 68 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.95-5666G>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140488151 | ||||||
chr4:140488170
|
A | G | 106 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0287others(103): Show | 111 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.95-5685T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140488170 | ||||||
chr4:140488268
|
T | C | 41 | a0001c0001t0001g0008a0001c0001t0001g0287a0001c0001t0001g0295others(38): Show | 43 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.95-5783A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140488268 | ||||||
chr4:140488390
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.95-5905T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140488390 | ||||||
chr4:140488436
|
C | T | 1 | a0001c0001t0010g0302 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.95-5951G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140488436 | ||||||
chr4:140488538
|
C | A | 111 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0073others(108): Show | 118 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.95-6053G>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140488538 | ||||||
chr4:140488583
|
C | T | 50 | a0002c0002t0001g0041a0002c0002t0002g0023a0002c0002t0003g0002others(47): Show | 52 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.95-6098G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140488583 | ||||||
chr4:140488602
|
A | G | 1 | a0001c0001t0002g0301 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.95-6117T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140488602 | ||||||
chr4:140488628
|
G | A | 1 | a0002c0002t0004g0059 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.95-6143C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140488628 | ||||||
chr4:140488693
|
T | A | 1 | a0001c0001t0001g0299 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.95-6208A>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140488693 | ||||||
chr4:140488737
|
T | G | 1 | a0002c0002t0003g0060 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.95-6252A>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140488737 | ||||||
chr4:140488789
|
T | C | 41 | a0001c0001t0001g0008a0001c0001t0001g0287a0001c0001t0001g0295others(38): Show | 43 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.95-6304A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140488789 | ||||||
chr4:140488820
|
C | G | 1 | a0002c0002t0003g0007 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.95-6335G>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140488820 | ||||||
chr4:140488864
|
T | A | 1 | a0002c0002t0003g0007 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.95-6379A>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140488864 | ||||||
chr4:140488945
|
T | C | 245 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0073others(242): Show | 253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.95-6460A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140488945 | ||||||
chr4:140489097
|
C | T | 112 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0073others(109): Show | 119 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.95-6612G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140489097 | ||||||
chr4:140489111
|
G | C | 33 | a0001c0001t0001g0261a0002c0002t0001g0245a0002c0002t0001g0276others(30): Show | 33 | HG00544.hp1 HG00609.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.95-6626C>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140489111 | ||||||
chr4:140489351
|
T | A | 1 | a0001c0001t0002g0300 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.95-6866A>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140489351 | ||||||
chr4:140489410
|
A | G | 3 | a0002c0002t0003g0016a0002c0002t0003g0017a0002c0002t0003g0018 | 3 | NA18989.hp2 NA18993.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.95-6925T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140489410 | ||||||
chr4:140489436
|
A | T | 9 | a0001c0001t0002g0271a0001c0001t0004g0275a0001c0001t0005g0239others(6): Show | 9 | HG02615.hp1 HG02647.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.95-6951T>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140489436 | ||||||
chr4:140489628
|
A | G | 2 | a0001c0001t0001g0111a0001c0001t0001g0112 | 2 | HG02818.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.95-7143T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140489628 | ||||||
chr4:140489723
|
A | G | 1 | a0001c0001t0001g0321 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.95-7238T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140489723 | ||||||
chr4:140490161
|
G | A | 1 | a0001c0001t0004g0275 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.95-7676C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140490161 | ||||||
chr4:140490269
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.95-7784C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140490269 | ||||||
chr4:140490595
|
C | T | 1 | a0001c0007t0004g0064 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.94+7534G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140490595 | ||||||
chr4:140490713
|
T | C | 2 | a0002c0005t0001g0083a0002c0005t0003g0082 | 2 | HG02040.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.94+7416A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140490713 | ||||||
chr4:140490976
|
C | T | 154 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0073others(151): Show | 161 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.94+7153G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140490976 | ||||||
chr4:140491028
|
T | A | 1 | a0002c0002t0003g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.94+7101A>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140491028 | ||||||
chr4:140491030
|
T | C | 1 | a0002c0002t0003g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.94+7099A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140491030 | ||||||
chr4:140491034
|
T | C | 1 | a0002c0002t0003g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.94+7095A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140491034 | ||||||
chr4:140491036
|
G | C | 1 | a0002c0002t0003g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.94+7093C>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140491036 | ||||||
chr4:140491037
|
T | A | 1 | a0002c0002t0003g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.94+7092A>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140491037 | ||||||
chr4:140491038
|
T | C | 1 | a0002c0002t0003g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.94+7091A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140491038 | ||||||
chr4:140491040
|
T | C | 1 | a0002c0002t0003g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.94+7089A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140491040 | ||||||
chr4:140491042
|
C | T | 1 | a0002c0002t0003g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.94+7087G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140491042 | ||||||
chr4:140491045
|
G | A | 1 | a0002c0002t0003g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.94+7084C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140491045 | ||||||
chr4:140491046
|
T | C | 1 | a0002c0002t0003g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.94+7083A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140491046 | ||||||
chr4:140491049
|
A | C | 1 | a0002c0002t0003g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.94+7080T>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140491049 | ||||||
chr4:140491050
|
G | T | 1 | a0002c0002t0003g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.94+7079C>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140491050 | ||||||
chr4:140491051
|
T | C | 1 | a0002c0002t0003g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.94+7078A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140491051 | ||||||
chr4:140491053
|
C | A | 1 | a0002c0002t0003g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.94+7076G>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140491053 | ||||||
chr4:140491055
|
A | C | 1 | a0002c0002t0003g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.94+7074T>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140491055 | ||||||
chr4:140491056
|
T | C | 1 | a0002c0002t0003g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.94+7073A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140491056 | ||||||
chr4:140491058
|
T | C | 1 | a0002c0002t0003g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.94+7071A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140491058 | ||||||
chr4:140491059
|
A | T | 1 | a0002c0002t0003g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.94+7070T>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140491059 | ||||||
chr4:140491061
|
C | G | 1 | a0002c0002t0003g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.94+7068G>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140491061 | ||||||
chr4:140491063
|
C | A | 1 | a0002c0002t0003g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.94+7066G>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140491063 | ||||||
chr4:140491066
|
T | A | 1 | a0002c0002t0003g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.94+7063A>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140491066 | ||||||
chr4:140491066
|
T | C | 1 | a0002c0002t0002g0270 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.94+7063A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140491066 | ||||||
chr4:140491069
|
C | A | 1 | a0002c0002t0003g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.94+7060G>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140491069 | ||||||
chr4:140491073
|
C | A | 1 | a0002c0002t0003g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.94+7056G>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140491073 | ||||||
chr4:140491078
|
A | C | 1 | a0002c0002t0003g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.94+7051T>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140491078 | ||||||
chr4:140491080
|
C | T | 1 | a0002c0002t0003g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.94+7049G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140491080 | ||||||
chr4:140491081
|
T | A | 1 | a0002c0002t0003g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.94+7048A>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140491081 | ||||||
chr4:140491082
|
T | C | 1 | a0002c0002t0003g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.94+7047A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140491082 | ||||||
chr4:140491083
|
T | C | 1 | a0002c0002t0003g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.94+7046A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140491083 | ||||||
chr4:140491096
|
T | G | 1 | a0002c0002t0003g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.94+7033A>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140491096 | ||||||
chr4:140491132
|
C | T | 1 | a0001c0001t0002g0271 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.94+6997G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140491132 | ||||||
chr4:140491151
|
T | G | 1 | a0001c0001t0002g0223 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.94+6978A>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140491151 | ||||||
chr4:140491334
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.94+6795C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140491334 | ||||||
chr4:140491370
|
C | T | 2 | a0001c0001t0001g0110a0001c0001t0013g0102 | 2 | HG01928.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.94+6759G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140491370 | ||||||
chr4:140491371
|
T | C | 1 | a0001c0001t0005g0244 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.94+6758A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140491371 | ||||||
chr4:140491532
|
C | A | 1 | a0001c0001t0002g0271 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.94+6597G>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140491532 | ||||||
chr4:140491722
|
G | A | 3 | a0002c0005t0001g0083a0002c0005t0003g0082a0002c0005t0004g0081 | 3 | HG02040.hp1 NA18939.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.94+6407C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140491722 | ||||||
chr4:140491769
|
A | G | 2 | a0001c0001t0002g0108a0001c0001t0002g0109 | 2 | HG03239.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.94+6360T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140491769 | ||||||
chr4:140491804
|
C | T | 3 | a0002c0005t0001g0083a0002c0005t0003g0082a0002c0005t0004g0081 | 3 | HG02040.hp1 NA18939.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.94+6325G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140491804 | ||||||
chr4:140491905
|
AG | A | 41 | a0001c0001t0001g0008a0001c0001t0001g0287a0001c0001t0001g0295others(38): Show | 43 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.94+6223delC | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140491905 | ||||||
chr4:140491923
|
G | C | 1 | a0001c0001t0001g0313 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.94+6206C>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140491923 | ||||||
chr4:140492161
|
A | G | 1 | a0002c0002t0002g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.94+5968T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140492161 | ||||||
chr4:140492379
|
T | G | 1 | a0001c0001t0002g0063 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.94+5750A>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140492379 | ||||||
chr4:140492511
|
C | T | 1 | a0001c0001t0005g0076 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.94+5618G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140492511 | ||||||
chr4:140492533
|
C | T | 56 | a0002c0002t0001g0041a0002c0002t0002g0023a0002c0002t0003g0002others(53): Show | 59 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.94+5596G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140492533 | ||||||
chr4:140492550
|
C | T | 3 | a0002c0005t0001g0083a0002c0005t0003g0082a0002c0005t0004g0081 | 3 | HG02040.hp1 NA18939.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.94+5579G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140492550 | ||||||
chr4:140492627
|
C | CA | 7 | a0001c0001t0001g0314a0001c0001t0002g0301a0001c0001t0003g0080others(4): Show | 7 | HG02040.hp1 HG02040.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.94+5501dupT | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140492627 | ||||||
chr4:140492627
|
CA | C | 8 | a0001c0001t0001g0073a0001c0001t0006g0004a0001c0001t0006g0005others(5): Show | 10 | HG01891.hp1 HG01943.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.94+5501delT | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140492627 | ||||||
chr4:140492627
|
CAA | C | 42 | a0001c0001t0001g0261a0001c0001t0002g0271a0001c0001t0004g0275others(39): Show | 42 | HG00544.hp1 HG00609.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.94+5500_94+5501del others(2): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140492627 | ||||||
chr4:140492643
|
A | T | 5 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(2): Show | 5 | HG00140.hp1 HG01106.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+5486T>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140492643 | ||||||
chr4:140492856
|
T | G | 154 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0073others(151): Show | 161 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.94+5273A>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140492856 | ||||||
chr4:140492967
|
T | C | 1 | a0001c0001t0010g0302 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.94+5162A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140492967 | ||||||
chr4:140493052
|
T | C | 12 | a0001c0001t0001g0303a0001c0001t0001g0304a0001c0001t0001g0305others(9): Show | 12 | HG02155.hp2 NA18960.hp2 NA18979.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+5077A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140493052 | ||||||
chr4:140493066
|
T | C | 112 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0073others(109): Show | 119 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.94+5063A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140493066 | ||||||
chr4:140493201
|
G | T | 36 | a0001c0001t0001g0261a0001c0001t0002g0271a0001c0001t0004g0275others(33): Show | 36 | HG00544.hp1 HG00609.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.94+4928C>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140493201 | ||||||
chr4:140493219
|
C | T | 1 | a0001c0001t0013g0102 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.94+4910G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140493219 | ||||||
chr4:140493287
|
C | CT | 16 | a0001c0001t0001g0079a0001c0001t0001g0089a0001c0001t0001g0090others(13): Show | 16 | HG00642.hp1 HG01169.hp2 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.94+4841dupA | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140493287 | ||||||
chr4:140493287
|
CT | C | 15 | a0001c0001t0001g0073a0001c0001t0001g0226a0001c0001t0001g0227others(12): Show | 17 | HG01891.hp1 HG02109.hp2 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.94+4841delA | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140493287 | ||||||
chr4:140493287
|
CTTTTTTT | C | 41 | a0001c0001t0001g0008a0001c0001t0001g0287a0001c0001t0001g0295others(38): Show | 43 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.94+4835_94+4841del others(7): Show |
MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140493287 | ||||||
chr4:140493400
|
A | G | 1 | a0001c0001t0001g0088 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.94+4729T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140493400 | ||||||
chr4:140493546
|
C | T | 68 | a0001c0001t0001g0073a0001c0001t0005g0066a0001c0001t0005g0076others(65): Show | 73 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.94+4583G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140493546 | ||||||
chr4:140493599
|
C | T | 7 | a0001c0001t0005g0239a0001c0001t0005g0240a0001c0001t0005g0241others(4): Show | 7 | HG02647.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+4530G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140493599 | ||||||
chr4:140493675
|
C | G | 1 | a0001c0001t0001g0087 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.94+4454G>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140493675 | ||||||
chr4:140493764
|
C | T | 2 | a0001c0001t0001g0065a0001c0007t0004g0064 | 2 | HG02451.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.94+4365G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140493764 | ||||||
chr4:140493932
|
A | G | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG01070.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.94+4197T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140493932 | ||||||
chr4:140494070
|
CA | C | 42 | a0001c0001t0001g0261a0001c0001t0002g0271a0001c0001t0004g0275others(39): Show | 42 | HG00544.hp1 HG00609.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.94+4058delT | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140494070 | ||||||
chr4:140494109
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.94+4020T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140494109 | ||||||
chr4:140494196
|
T | C | 1 | a0001c0001t0005g0274 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.94+3933A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140494196 | ||||||
chr4:140494356
|
A | C | 3 | a0002c0005t0001g0083a0002c0005t0003g0082a0002c0005t0004g0081 | 3 | HG02040.hp1 NA18939.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.94+3773T>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140494356 | ||||||
chr4:140494483
|
T | C | 10 | a0002c0002t0002g0078a0002c0002t0002g0229a0002c0002t0002g0230others(7): Show | 11 | HG00738.hp2 HG01255.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.94+3646A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140494483 | ||||||
chr4:140494564
|
C | T | 42 | a0001c0001t0001g0261a0001c0001t0002g0271a0001c0001t0004g0275others(39): Show | 42 | HG00544.hp1 HG00609.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.94+3565G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140494564 | ||||||
chr4:140494772
|
C | T | 2 | a0001c0001t0001g0079a0001c0001t0003g0080 | 2 | HG02602.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.94+3357G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140494772 | ||||||
chr4:140494816
|
T | C | 154 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0073others(151): Show | 161 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.94+3313A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140494816 | ||||||
chr4:140494861
|
C | T | 42 | a0001c0001t0001g0261a0001c0001t0002g0271a0001c0001t0004g0275others(39): Show | 42 | HG00544.hp1 HG00609.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.94+3268G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140494861 | ||||||
chr4:140494940
|
T | A | 1 | a0001c0001t0003g0236 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.94+3189A>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140494940 | ||||||
chr4:140494946
|
A | G | 154 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0073others(151): Show | 161 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.94+3183T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140494946 | ||||||
chr4:140495209
|
C | T | 1 | a0002c0002t0002g0078 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.94+2920G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140495209 | ||||||
chr4:140495311
|
A | G | 1 | a0001c0001t0001g0077 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.94+2818T>C | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140495311 | ||||||
chr4:140495674
|
C | T | 42 | a0001c0001t0001g0261a0001c0001t0002g0271a0001c0001t0004g0275others(39): Show | 42 | HG00544.hp1 HG00609.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.94+2455G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140495674 | ||||||
chr4:140495769
|
C | T | 41 | a0001c0001t0001g0008a0001c0001t0001g0287a0001c0001t0001g0295others(38): Show | 43 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.94+2360G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140495769 | ||||||
chr4:140495795
|
G | A | 1 | a0001c0001t0004g0275 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.94+2334C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140495795 | ||||||
chr4:140495806
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.94+2323C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140495806 | ||||||
chr4:140496624
|
C | A | 1 | a0001c0001t0004g0275 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.94+1505G>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140496624 | ||||||
chr4:140496837
|
T | TA | 77 | a0001c0001t0001g0065a0001c0001t0001g0073a0001c0001t0002g0315others(74): Show | 82 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.94+1291dupT | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140496837 | ||||||
chr4:140496929
|
G | A | 1 | a0001c0001t0002g0318 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.94+1200C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140496929 | ||||||
chr4:140497158
|
C | T | 71 | a0001c0001t0001g0065a0001c0001t0001g0073a0001c0001t0005g0066others(68): Show | 76 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.94+971G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140497158 | ||||||
chr4:140497363
|
G | C | 1 | a0001c0001t0001g0319 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.94+766C>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140497363 | ||||||
chr4:140497706
|
C | T | 1 | a0001c0001t0002g0063 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.94+423G>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140497706 | ||||||
chr4:140497927
|
G | A | 1 | a0005c0008t0001g0238 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.94+202C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140497927 | ||||||
chr4:140497929
|
G | C | 42 | a0001c0001t0001g0261a0001c0001t0002g0271a0001c0001t0004g0275others(39): Show | 42 | HG00544.hp1 HG00609.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.94+200C>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140497929 | ||||||
chr4:140498019
|
G | A | 41 | a0001c0001t0001g0008a0001c0001t0001g0287a0001c0001t0001g0295others(38): Show | 43 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.94+110C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140498019 | ||||||
chr4:140498072
|
T | C | 1 | a0001c0001t0011g0320 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.94+57A>G | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140498072 | ||||||
chr4:140498111
|
G | A | 2 | a0001c0001t0001g0321a0001c0001t0001g0322 | 2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.94+18C>T | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140498111 | ||||||
chr4:140498120
|
G | T | 56 | a0002c0002t0001g0041a0002c0002t0002g0023a0002c0002t0003g0002others(53): Show | 59 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.94+9C>A | MGAT4D | ENSG00000205301.12 | transcript | ENST00000511113.6 | protein_coding | 1/10 | chr4 | 140498120 |