geneid | 8702 |
---|---|
ensemblid | ENSG00000121578.13 |
hgncid | 927 |
symbol | B4GALT4 |
name | beta-1,4-galactosyltransferase 4 |
refseq_nuc | NM_003778.4 |
refseq_prot | NP_003769.1 |
ensembl_nuc | ENST00000393765.7 |
ensembl_prot | ENSP00000377360.2 |
mane_status | MANE Select |
chr | chr3 |
start | 119211742 |
end | 119240878 |
strand | - |
ver | v1.2 |
region | chr3:119211742-119240878 |
region5000 | chr3:119206742-119245878 |
regionname0 | B4GALT4_chr3_119211742_119240878 |
regionname5000 | B4GALT4_chr3_119206742_119245878 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 344 | 295 | 66 | 53 | 134 | 15 | 25 | 107 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
a0002 | 0/0 | 344 | 138 | 27 | 23 | 72 | 1 | 15 | 57 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
a0003 | 0/0 | 344 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
a0004 | 0/0 | 344 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1035 | 206 | 58 | 36 | 81 | 10 | 19 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
c0002 | 0/0 | 1035 | 137 | 27 | 23 | 71 | 1 | 15 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
c0003 | 0/0 | 1035 | 82 | 1 | 17 | 53 | 5 | 6 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
c0004 | 0/0 | 1035 | 3 | 3 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
c0005 | 0/0 | 1035 | 3 | 3 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
c0006 | 0/0 | 1035 | 2 | 0 | 0 | 0 | 0 | 2 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
c0007 | 0/0 | 1035 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
c0008 | 0/0 | 1035 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
c0009 | 0/0 | 1035 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1200 | 155 | 31 | 16 | 100 | 1 | 7 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
t0002 | 0/1 | 1200 | 118 | 6 | 24 | 63 | 7 | 17 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
t0003 | 0/0 | 1200 | 70 | 16 | 16 | 23 | 8 | 7 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
t0004 | 0/0 | 1200 | 35 | 7 | 3 | 16 | 0 | 9 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
t0005 | 0/0 | 1200 | 13 | 0 | 11 | 0 | 0 | 2 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
t0006 | 0/0 | 1200 | 9 | 8 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
t0007 | 1/0 | 1200 | 8 | 5 | 2 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
t0008 | 0/0 | 1200 | 5 | 5 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
t0009 | 0/0 | 1200 | 5 | 2 | 1 | 2 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
t0010 | 0/0 | 1200 | 3 | 3 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
t0011 | 0/0 | 1200 | 3 | 3 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
t0012 | 0/0 | 1200 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
t0013 | 0/0 | 1200 | 2 | 0 | 2 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
t0014 | 0/0 | 1200 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
t0015 | 0/0 | 1200 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
t0016 | 0/0 | 1200 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
t0017 | 0/0 | 1200 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
t0018 | 0/0 | 1200 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
t0019 | 0/0 | 1200 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
t0020 | 0/0 | 1200 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 38 | 0 | 15 | 16 | 4 | 3 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0002 | 0/0 | 28 | 0 | 2 | 25 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0003 | 0/0 | 16 | 0 | 6 | 4 | 4 | 2 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0004 | 0/0 | 12 | 0 | 1 | 4 | 0 | 7 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0005 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0006 | 0/1 | 9 | 0 | 1 | 4 | 0 | 3 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0007 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0008 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0009 | 0/0 | 7 | 1 | 0 | 6 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0010 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0011 | 1/0 | 7 | 4 | 2 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0012 | 0/0 | 6 | 0 | 4 | 0 | 0 | 2 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0014 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0015 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0016 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0018 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0019 | 0/0 | 4 | 0 | 1 | 2 | 1 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0020 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0024 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0025 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0047 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0054 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1035 | 206 | 58 | 36 | 81 | 10 | 19 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
a0001c0003 | 0/0 | 1035 | 82 | 1 | 17 | 53 | 5 | 6 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
a0001c0004 | 0/0 | 1035 | 3 | 3 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
a0001c0005 | 0/0 | 1035 | 3 | 3 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
a0001c0009 | 0/0 | 1035 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
a0002c0002 | 0/0 | 1035 | 137 | 27 | 23 | 71 | 1 | 15 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
a0002c0008 | 0/0 | 1035 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
a0003c0006 | 0/0 | 1035 | 2 | 0 | 0 | 0 | 0 | 2 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
a0004c0007 | 0/0 | 1035 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2234 | 79 | 26 | 9 | 41 | 0 | 3 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
a0001c0001t0002 | 0/1 | 2234 | 41 | 5 | 7 | 17 | 2 | 9 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
a0001c0001t0003 | 0/0 | 2234 | 70 | 16 | 16 | 23 | 8 | 7 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
a0001c0001t0007 | 1/0 | 2234 | 8 | 5 | 2 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
a0001c0001t0009 | 0/0 | 2234 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
a0001c0001t0012 | 0/0 | 2234 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
a0001c0001t0013 | 0/0 | 2234 | 2 | 0 | 2 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
a0001c0001t0014 | 0/0 | 2234 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
a0001c0001t0018 | 0/0 | 2234 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
a0001c0003t0001 | 0/0 | 2234 | 4 | 1 | 0 | 3 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
a0001c0003t0002 | 0/0 | 2234 | 74 | 0 | 17 | 46 | 5 | 6 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
a0001c0003t0009 | 0/0 | 2234 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
a0001c0003t0016 | 0/0 | 2234 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
a0001c0003t0020 | 0/0 | 2234 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
a0001c0004t0001 | 0/0 | 2234 | 3 | 3 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
a0001c0005t0010 | 0/0 | 2234 | 3 | 3 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
a0001c0009t0002 | 0/0 | 2234 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
a0002c0002t0001 | 0/0 | 2234 | 68 | 1 | 7 | 55 | 1 | 4 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
a0002c0002t0004 | 0/0 | 2234 | 35 | 7 | 3 | 16 | 0 | 9 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
a0002c0002t0005 | 0/0 | 2234 | 13 | 0 | 11 | 0 | 0 | 2 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
a0002c0002t0006 | 0/0 | 2234 | 8 | 7 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
a0002c0002t0008 | 0/0 | 2234 | 5 | 5 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
a0002c0002t0009 | 0/0 | 2234 | 2 | 1 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
a0002c0002t0011 | 0/0 | 2234 | 3 | 3 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
a0002c0002t0015 | 0/0 | 2234 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
a0002c0002t0017 | 0/0 | 2234 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
a0002c0002t0019 | 0/0 | 2234 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
a0002c0008t0001 | 0/0 | 2234 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
a0003c0006t0002 | 0/0 | 2234 | 2 | 0 | 0 | 0 | 0 | 2 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
a0004c0007t0006 | 0/0 | 2234 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | copy fasta | chr3 | 119206742 | 119245878 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0001g0009 | 0/0 | 7 | 1 | 0 | 6 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0001g0010 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0001g0014 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0001g0015 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0001g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0002g0006 | 0/1 | 9 | 0 | 1 | 4 | 0 | 3 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0002g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0002g0025 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0002g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0003 | 0/0 | 16 | 0 | 6 | 4 | 4 | 2 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0018 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0007g0011 | 1/0 | 7 | 4 | 2 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0007g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0009g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0012g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0012g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0013g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0014g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0001t0018g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0003t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0003t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0003t0002g0001 | 0/0 | 38 | 0 | 15 | 16 | 4 | 3 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0003t0002g0007 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0003t0002g0019 | 0/0 | 4 | 0 | 1 | 2 | 1 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0003t0002g0047 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0003t0002g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0003t0002g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0003t0002g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0003t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0003t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0003t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0003t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0003t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0003t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0003t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0003t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0003t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0003t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0003t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0003t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0003t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0003t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0003t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0003t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0003t0009g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0003t0009g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0003t0016g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0003t0020g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0004t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0004t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0005t0010g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0005t0010g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0001c0009t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0001g0002 | 0/0 | 28 | 0 | 2 | 25 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0001g0008 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0001g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0004g0004 | 0/0 | 12 | 0 | 1 | 4 | 0 | 7 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0004g0016 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0004g0020 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0004g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0004g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0004g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0004g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0004g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0005g0012 | 0/0 | 6 | 0 | 4 | 0 | 0 | 2 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0005g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0005g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0005g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0005g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0005g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0005g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0006g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0006g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0006g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0006g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0006g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0006g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0006g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0008g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0008g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0008g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0009g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0009g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0011g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0011g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0015g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0017g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0002t0019g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0002c0008t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0003c0006t0002g0054 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
a0004c0007t0006g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0077 | EUR | GBR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | GBR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0158 | EUR | GBR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0025 | EUR | GBR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0156 | EUR | FIN | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | FIN | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | FIN | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG00323 | hp2 | a0001 | c0003 | t0002 | g0001 | EUR | FIN | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG00423 | hp1 | a0001 | c0003 | t0002 | g0001 | EAS | CHS | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG00423 | hp2 | a0002 | c0002 | t0004 | g0016 | EAS | CHS | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG00438 | hp1 | a0001 | c0003 | t0002 | g0001 | EAS | CHS | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | CHS | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0144 | EAS | CHS | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG00544 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0090 | EAS | CHS | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | CHS | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG00609 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | CHS | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0149 | EAS | CHS | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | CHS | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0168 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG00639 | hp2 | a0002 | c0002 | t0004 | g0020 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG00642 | hp1 | a0001 | c0001 | t0013 | g0042 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG00673 | hp1 | a0001 | c0003 | t0002 | g0001 | EAS | CHS | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG00733 | hp2 | a0001 | c0003 | t0002 | g0001 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG00735 | hp1 | a0002 | c0002 | t0005 | g0012 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0174 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0152 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG00741 | hp2 | a0001 | c0003 | t0002 | g0001 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01069 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01069 | hp2 | a0001 | c0003 | t0002 | g0019 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01070 | hp2 | a0002 | c0002 | t0005 | g0012 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01074 | hp1 | a0002 | c0002 | t0005 | g0076 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01081 | hp1 | a0002 | c0002 | t0005 | g0064 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01081 | hp2 | a0002 | c0002 | t0005 | g0012 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0166 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01099 | hp2 | a0001 | c0001 | t0007 | g0011 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01106 | hp1 | a0002 | c0002 | t0006 | g0070 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01106 | hp2 | a0001 | c0003 | t0002 | g0001 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01109 | hp2 | a0001 | c0003 | t0002 | g0001 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01167 | hp2 | a0001 | c0001 | t0013 | g0042 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01168 | hp1 | a0001 | c0003 | t0002 | g0001 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0157 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01192 | hp2 | a0001 | c0003 | t0002 | g0001 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01243 | hp1 | a0002 | c0002 | t0001 | g0029 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01243 | hp2 | a0001 | c0001 | t0007 | g0011 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01255 | hp2 | a0002 | c0002 | t0001 | g0086 | AMR | CLM | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01256 | hp1 | a0001 | c0003 | t0002 | g0047 | AMR | CLM | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01258 | hp2 | a0001 | c0003 | t0002 | g0001 | AMR | CLM | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01346 | hp1 | a0001 | c0003 | t0002 | g0001 | AMR | CLM | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01358 | hp1 | a0001 | c0003 | t0002 | g0001 | AMR | CLM | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01358 | hp2 | a0002 | c0002 | t0005 | g0092 | AMR | CLM | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0123 | AMR | CLM | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01361 | hp2 | a0002 | c0002 | t0005 | g0012 | AMR | CLM | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0115 | AMR | CLM | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01496 | hp2 | a0001 | c0003 | t0002 | g0001 | AMR | CLM | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01515 | hp1 | a0001 | c0003 | t0002 | g0001 | EUR | IBS | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | IBS | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01516 | hp1 | a0001 | c0003 | t0002 | g0019 | EUR | IBS | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0025 | EUR | IBS | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01884 | hp1 | a0002 | c0002 | t0008 | g0026 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01884 | hp2 | a0001 | c0004 | t0001 | g0091 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01891 | hp2 | a0002 | c0002 | t0015 | g0119 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0160 | AMR | PEL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01934 | hp2 | a0002 | c0002 | t0005 | g0075 | AMR | PEL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0081 | AMR | PEL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01943 | hp2 | a0002 | c0002 | t0005 | g0031 | AMR | PEL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PEL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01952 | hp2 | a0002 | c0002 | t0004 | g0192 | AMR | PEL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0093 | AMR | PEL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01975 | hp2 | a0002 | c0002 | t0004 | g0004 | AMR | PEL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01978 | hp1 | a0001 | c0003 | t0002 | g0001 | AMR | PEL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01978 | hp2 | a0002 | c0002 | t0005 | g0031 | AMR | PEL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01981 | hp1 | a0001 | c0003 | t0002 | g0001 | AMR | PEL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01993 | hp1 | a0002 | c0002 | t0005 | g0063 | AMR | PEL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01993 | hp2 | a0001 | c0003 | t0002 | g0001 | AMR | PEL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02015 | hp2 | a0002 | c0002 | t0001 | g0032 | EAS | KHV | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02027 | hp1 | a0001 | c0003 | t0002 | g0001 | EAS | KHV | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02027 | hp2 | a0002 | c0002 | t0001 | g0094 | EAS | KHV | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02055 | hp1 | a0001 | c0001 | t0014 | g0046 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02055 | hp2 | a0001 | c0003 | t0001 | g0130 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | KHV | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02071 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02071 | hp2 | a0001 | c0003 | t0002 | g0214 | EAS | KHV | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02080 | hp1 | a0001 | c0003 | t0002 | g0051 | EAS | KHV | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | KHV | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02083 | hp1 | a0002 | c0002 | t0001 | g0082 | EAS | KHV | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02129 | hp2 | a0001 | c0003 | t0001 | g0038 | EAS | KHV | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02132 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | KHV | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | KHV | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02145 | hp1 | a0002 | c0002 | t0004 | g0116 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02148 | hp1 | a0001 | c0001 | t0003 | g0154 | AMR | PEL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02148 | hp2 | a0002 | c0002 | t0009 | g0151 | AMR | PEL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02155 | hp1 | a0001 | c0003 | t0002 | g0211 | EAS | CDX | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02155 | hp2 | a0001 | c0003 | t0002 | g0001 | EAS | CDX | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CDX | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02165 | hp2 | a0001 | c0003 | t0016 | g0207 | EAS | CDX | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02257 | hp1 | a0001 | c0001 | t0018 | g0073 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02257 | hp2 | a0002 | c0002 | t0006 | g0034 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02258 | hp1 | a0001 | c0001 | t0012 | g0133 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02258 | hp2 | a0002 | c0002 | t0001 | g0117 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02293 | hp1 | a0001 | c0003 | t0002 | g0001 | AMR | PEL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0018 | AMR | PEL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0080 | AMR | PEL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02300 | hp2 | a0001 | c0003 | t0002 | g0001 | AMR | PEL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0164 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02451 | hp2 | a0002 | c0002 | t0011 | g0045 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02572 | hp2 | a0001 | c0004 | t0001 | g0030 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02602 | hp1 | a0002 | c0002 | t0001 | g0088 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0155 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0179 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02615 | hp2 | a0002 | c0002 | t0004 | g0079 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02622 | hp1 | a0002 | c0002 | t0008 | g0098 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02622 | hp2 | a0002 | c0002 | t0011 | g0169 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02630 | hp2 | a0002 | c0002 | t0006 | g0071 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02647 | hp1 | a0001 | c0001 | t0007 | g0011 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02647 | hp2 | a0002 | c0002 | t0006 | g0065 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0105 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02698 | hp1 | a0001 | c0003 | t0002 | g0001 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02698 | hp2 | a0002 | c0002 | t0004 | g0004 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02717 | hp2 | a0001 | c0004 | t0001 | g0030 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02723 | hp1 | a0002 | c0002 | t0019 | g0181 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02723 | hp2 | a0001 | c0001 | t0007 | g0190 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02735 | hp2 | a0002 | c0002 | t0001 | g0060 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0148 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02738 | hp2 | a0002 | c0002 | t0004 | g0004 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0170 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0177 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02886 | hp1 | a0002 | c0002 | t0011 | g0045 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0167 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0163 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0178 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02896 | hp1 | a0002 | c0002 | t0008 | g0026 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0185 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0147 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02897 | hp2 | a0002 | c0002 | t0008 | g0026 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0191 | AFR | ESN | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02976 | hp1 | a0002 | c0002 | t0004 | g0198 | AFR | ESN | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03017 | hp2 | a0002 | c0002 | t0004 | g0187 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03041 | hp2 | a0001 | c0005 | t0010 | g0035 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03098 | hp2 | a0002 | c0002 | t0004 | g0196 | AFR | MSL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | ESN | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03195 | hp1 | a0004 | c0007 | t0006 | g0129 | AFR | ESN | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03209 | hp1 | a0001 | c0001 | t0009 | g0165 | AFR | MSL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03209 | hp2 | a0001 | c0005 | t0010 | g0035 | AFR | MSL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03225 | hp1 | a0001 | c0001 | t0007 | g0011 | AFR | MSL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03225 | hp2 | a0002 | c0002 | t0009 | g0150 | AFR | MSL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03239 | hp2 | a0001 | c0003 | t0002 | g0001 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03486 | hp2 | a0002 | c0002 | t0006 | g0066 | AFR | MSL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03491 | hp1 | a0002 | c0002 | t0004 | g0004 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03491 | hp2 | a0003 | c0006 | t0002 | g0054 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03492 | hp2 | a0002 | c0002 | t0004 | g0004 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03516 | hp1 | a0002 | c0002 | t0004 | g0072 | AFR | ESN | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03540 | hp2 | a0002 | c0002 | t0006 | g0069 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03579 | hp1 | a0002 | c0002 | t0006 | g0034 | AFR | MSL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | MSL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0182 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03654 | hp2 | a0002 | c0002 | t0005 | g0012 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0121 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03669 | hp2 | a0003 | c0006 | t0002 | g0054 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03704 | hp2 | a0002 | c0002 | t0004 | g0004 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0120 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03831 | hp1 | a0002 | c0002 | t0004 | g0004 | SAS | BEB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | BEB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03834 | hp1 | a0001 | c0003 | t0002 | g0186 | SAS | BEB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0108 | SAS | BEB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0124 | SAS | BEB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0161 | SAS | BEB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG04184 | hp1 | a0001 | c0003 | t0002 | g0206 | SAS | BEB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0153 | SAS | BEB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG04199 | hp1 | a0002 | c0002 | t0005 | g0012 | SAS | STU | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG04199 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | STU | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG04204 | hp1 | a0001 | c0003 | t0002 | g0208 | SAS | STU | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG04204 | hp2 | a0002 | c0002 | t0004 | g0193 | SAS | STU | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG04228 | hp1 | a0001 | c0003 | t0002 | g0001 | SAS | STU | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0109 | SAS | STU | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18522 | hp1 | a0001 | c0005 | t0010 | g0055 | AFR | YRI | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | YRI | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18612 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18747 | hp1 | a0002 | c0002 | t0004 | g0016 | EAS | CHB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18747 | hp2 | a0001 | c0003 | t0002 | g0007 | EAS | CHB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | YRI | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18906 | hp2 | a0002 | c0002 | t0017 | g0195 | AFR | YRI | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18940 | hp2 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18941 | hp1 | a0001 | c0003 | t0002 | g0007 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18941 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18942 | hp2 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18943 | hp2 | a0001 | c0003 | t0002 | g0001 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18944 | hp1 | a0002 | c0002 | t0004 | g0048 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18945 | hp2 | a0001 | c0003 | t0002 | g0007 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18946 | hp1 | a0002 | c0002 | t0004 | g0016 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18946 | hp2 | a0001 | c0003 | t0002 | g0059 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18947 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18948 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18949 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18950 | hp2 | a0002 | c0002 | t0004 | g0004 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18953 | hp1 | a0001 | c0003 | t0002 | g0001 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18953 | hp2 | a0001 | c0003 | t0002 | g0050 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18954 | hp1 | a0001 | c0003 | t0002 | g0001 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18956 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18956 | hp2 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18959 | hp1 | a0002 | c0002 | t0004 | g0184 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18959 | hp2 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18961 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18963 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18966 | hp2 | a0001 | c0003 | t0002 | g0007 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18967 | hp2 | a0002 | c0002 | t0004 | g0004 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18968 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18969 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18969 | hp2 | a0001 | c0003 | t0002 | g0047 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18970 | hp2 | a0001 | c0003 | t0002 | g0213 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18975 | hp1 | a0001 | c0003 | t0002 | g0215 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18975 | hp2 | a0002 | c0008 | t0001 | g0087 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18977 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18978 | hp1 | a0001 | c0003 | t0002 | g0001 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18978 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18979 | hp1 | a0001 | c0003 | t0002 | g0210 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18980 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18980 | hp2 | a0001 | c0003 | t0002 | g0001 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18982 | hp1 | a0001 | c0003 | t0002 | g0001 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18982 | hp2 | a0002 | c0002 | t0004 | g0049 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18985 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18985 | hp2 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18986 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18988 | hp1 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18988 | hp2 | a0002 | c0002 | t0004 | g0199 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18989 | hp1 | a0001 | c0003 | t0002 | g0052 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18989 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18991 | hp2 | a0001 | c0003 | t0002 | g0019 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18993 | hp1 | a0001 | c0003 | t0002 | g0205 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18994 | hp2 | a0001 | c0003 | t0001 | g0113 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18995 | hp1 | a0002 | c0002 | t0004 | g0048 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18995 | hp2 | a0001 | c0003 | t0002 | g0001 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18997 | hp1 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18997 | hp2 | a0001 | c0003 | t0002 | g0201 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18998 | hp1 | a0001 | c0003 | t0002 | g0001 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18999 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18999 | hp2 | a0002 | c0002 | t0004 | g0016 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19000 | hp2 | a0001 | c0003 | t0001 | g0038 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19003 | hp1 | a0002 | c0002 | t0004 | g0004 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19003 | hp2 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19006 | hp1 | a0001 | c0003 | t0020 | g0223 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19006 | hp2 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19009 | hp1 | a0001 | c0003 | t0002 | g0052 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19009 | hp2 | a0001 | c0003 | t0002 | g0200 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19011 | hp1 | a0001 | c0003 | t0002 | g0051 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19012 | hp1 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19012 | hp2 | a0002 | c0002 | t0004 | g0016 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | LWK | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0162 | AFR | LWK | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | LWK | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19043 | hp2 | a0001 | c0001 | t0014 | g0046 | AFR | LWK | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19054 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19057 | hp2 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19058 | hp2 | a0002 | c0002 | t0004 | g0188 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19060 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19062 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19063 | hp1 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19063 | hp2 | a0002 | c0002 | t0004 | g0049 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19064 | hp1 | a0001 | c0003 | t0002 | g0007 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19065 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19066 | hp2 | a0001 | c0003 | t0002 | g0204 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19067 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19067 | hp2 | a0001 | c0003 | t0002 | g0202 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19074 | hp1 | a0001 | c0003 | t0002 | g0001 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19074 | hp2 | a0001 | c0003 | t0009 | g0180 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19075 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19075 | hp2 | a0001 | c0003 | t0002 | g0216 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19078 | hp1 | a0001 | c0003 | t0002 | g0209 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19080 | hp1 | a0001 | c0003 | t0002 | g0001 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19081 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19082 | hp2 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19084 | hp2 | a0001 | c0003 | t0002 | g0007 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19086 | hp1 | a0001 | c0003 | t0002 | g0050 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19087 | hp1 | a0001 | c0003 | t0002 | g0007 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19088 | hp1 | a0001 | c0003 | t0002 | g0001 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19090 | hp2 | a0001 | c0003 | t0002 | g0007 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19091 | hp1 | a0001 | c0003 | t0009 | g0217 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19091 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19240 | hp1 | a0001 | c0009 | t0002 | g0096 | AFR | YRI | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA19240 | hp2 | a0002 | c0002 | t0004 | g0020 | AFR | YRI | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ASW | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0183 | AFR | ASW | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0159 | EUR | TSI | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA20752 | hp2 | a0001 | c0003 | t0002 | g0001 | EUR | TSI | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0218 | EUR | TSI | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA20805 | hp2 | a0001 | c0003 | t0002 | g0001 | EUR | TSI | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA20905 | hp1 | a0002 | c0002 | t0004 | g0004 | SAS | GIH | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0085 | SAS | GIH | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0122 | AMR | CLM | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG01123 | hp2 | a0001 | c0001 | t0003 | g0018 | AMR | CLM | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02109 | hp1 | a0001 | c0001 | t0012 | g0189 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02109 | hp2 | a0001 | c0001 | t0007 | g0011 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02486 | hp1 | a0002 | c0002 | t0008 | g0134 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0171 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG02559 | hp2 | a0002 | c0002 | t0004 | g0020 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0176 | AFR | MSL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
HG03471 | hp2 | a0001 | c0001 | t0007 | g0011 | AFR | MSL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18955 | hp1 | a0002 | c0002 | t0004 | g0004 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA18955 | hp2 | a0001 | c0003 | t0002 | g0019 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | USA | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA20300 | hp2 | a0002 | c0002 | t0006 | g0067 | AFR | USA | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | LWK | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | LWK | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0006 | REF | REF | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0007 | g0011 | REF | REF | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:119212554
|
C | A | 1 | a0003 | 2 | HG03491.hp2 HG03669.hp2 |
missense_variant | MODERATE | c.1030G>T | p.Ala344Ser | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 8/8 | 1422/2234 | 1030/1035 | 344/344 | chr3 | 119212554 | ||
chr3:119212556
|
C | T | 1 | a0004 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.1028G>A | p.Gly343Asp | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 8/8 | 1420/2234 | 1028/1035 | 343/344 | chr3 | 119212556 | ||
chr3:119226949
|
G | C | 2 | a0002a0004 | 139 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(136): Show |
missense_variant | MODERATE | c.346C>G | p.Gln116Glu | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/8 | 738/2234 | 346/1035 | 116/344 | chr3 | 119226949 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:119224213
|
G | A | 1 | a0001c0004 | 3 | HG01884.hp2 HG02572.hp2 HG02717.hp2 |
synonymous_variant | LOW | c.519C>T | p.Leu173Leu | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/8 | 911/2234 | 519/1035 | 173/344 | chr3 | 119224213 | ||
chr3:119229848
|
G | A | 1 | a0002c0008 | 1 | NA18975.hp2 | splice_region_variant&synonymous_variant | LOW | c.252C>T | p.Leu84Leu | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/8 | 644/2234 | 252/1035 | 84/344 | chr3 | 119229848 | ||
chr3:119229869
|
G | A | 2 | a0001c0003a0001c0009 | 83 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(80): Show |
synonymous_variant | LOW | c.231C>T | p.Cys77Cys | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/8 | 623/2234 | 231/1035 | 77/344 | chr3 | 119229869 | ||
chr3:119229998
|
G | A | 2 | a0001c0005a0001c0009 | 4 | HG03041.hp2 HG03209.hp2 NA18522.hp1 others(1): Show |
synonymous_variant | LOW | c.102C>T | p.Phe34Phe | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/8 | 494/2234 | 102/1035 | 34/344 | chr3 | 119229998 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:119211797
|
T | C | 1 | a0001c0003t0016 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*752A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 8/8 | 752 | chr3 | 119211797 | |||||
chr3:119211896
|
T | A | 1 | a0002c0002t0017 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*653A>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 8/8 | 653 | chr3 | 119211896 | |||||
chr3:119211944
|
G | C | 10 | a0001c0001t0002a0001c0001t0003a0001c0001t0013others(7): Show | 197 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*605C>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 8/8 | 605 | chr3 | 119211944 | |||||
chr3:119211962
|
A | G | 4 | a0001c0001t0018a0002c0002t0006a0002c0002t0011others(1): Show | 13 | HG01106.hp1 HG02257.hp1 HG02257.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*587T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 8/8 | 587 | chr3 | 119211962 | |||||
chr3:119211980
|
G | A | 2 | a0002c0002t0005a0002c0002t0015 | 14 | HG00735.hp1 HG01070.hp2 HG01074.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*569C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 8/8 | 569 | chr3 | 119211980 | |||||
chr3:119212037
|
G | A | 9 | a0002c0002t0004a0002c0002t0005a0002c0002t0006others(6): Show | 68 | HG00423.hp2 HG00639.hp2 HG00735.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*512C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 8/8 | 512 | chr3 | 119212037 | |||||
chr3:119212055
|
T | C | 1 | a0001c0001t0018 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*494A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 8/8 | 494 | chr3 | 119212055 | |||||
chr3:119212266
|
C | T | 3 | a0002c0002t0005a0002c0002t0008a0002c0002t0015 | 19 | HG00735.hp1 HG01070.hp2 HG01074.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*283G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 8/8 | 283 | chr3 | 119212266 | |||||
chr3:119212438
|
C | A | 1 | a0001c0001t0013 | 2 | HG00642.hp1 HG01167.hp2 |
3_prime_UTR_variant | MODIFIER | c.*111G>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 8/8 | 111 | chr3 | 119212438 | |||||
chr3:119212474
|
C | T | 1 | a0001c0001t0012 | 2 | HG02109.hp1 HG02258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*75G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 8/8 | 75 | chr3 | 119212474 | |||||
chr3:119212542
|
C | T | 23 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(20): Show | 397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
3_prime_UTR_variant | MODIFIER | c.*7G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 8/8 | 7 | chr3 | 119212542 | |||||
chr3:119230131
|
C | A | 1 | a0001c0005t0010 | 3 | HG03041.hp2 HG03209.hp2 NA18522.hp1 |
5_prime_UTR_variant | MODIFIER | c.-32G>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/8 | 32 | chr3 | 119230131 | |||||
chr3:119230184
|
G | A | 1 | a0001c0001t0014 | 2 | HG02055.hp1 NA19043.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-85C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/8 | chr3 | 119230184 | ||||||
chr3:119236988
|
C | T | 1 | a0002c0002t0015 | 1 | HG01891.hp2 | 5_prime_UTR_variant | MODIFIER | c.-281G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/8 | 6889 | chr3 | 119236988 | |||||
chr3:119237006
|
T | C | 1 | a0001c0005t0010 | 3 | HG03041.hp2 HG03209.hp2 NA18522.hp1 |
5_prime_UTR_variant | MODIFIER | c.-299A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/8 | 6907 | chr3 | 119237006 | |||||
chr3:119237041
|
G | A | 8 | a0001c0001t0003a0001c0001t0009a0001c0001t0013others(5): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(80): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-334C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/8 | chr3 | 119237041 | ||||||
chr3:119240874
|
G | C | 1 | a0001c0003t0020 | 1 | NA19006.hp1 | 5_prime_UTR_variant | MODIFIER | c.-388C>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/8 | 10775 | chr3 | 119240874 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:119212694
|
A | G | 1 | a0002c0002t0001g0077 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.903-13T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119212694 | ||||||
chr3:119212822
|
G | T | 221 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(218): Show | 428 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(425): Show |
intron_variant | MODIFIER | c.903-141C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119212822 | ||||||
chr3:119213188
|
G | T | 6 | a0002c0002t0006g0067a0002c0002t0006g0069a0002c0002t0006g0070others(3): Show | 7 | HG01106.hp1 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.903-507C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119213188 | ||||||
chr3:119213240
|
G | A | 1 | a0001c0001t0003g0171 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.903-559C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119213240 | ||||||
chr3:119213280
|
G | A | 2 | a0001c0001t0003g0155a0001c0001t0003g0161 | 2 | HG02602.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.903-599C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119213280 | ||||||
chr3:119213338
|
C | T | 1 | a0001c0001t0018g0073 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.903-657G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119213338 | ||||||
chr3:119213354
|
T | C | 1 | a0001c0001t0001g0220 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.903-673A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119213354 | ||||||
chr3:119213601
|
T | C | 11 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0053others(8): Show | 28 | HG00408.hp1 HG02083.hp2 HG02129.hp1 others(25): Show |
intron_variant | MODIFIER | c.903-920A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119213601 | ||||||
chr3:119213980
|
T | G | 2 | a0002c0002t0001g0117a0002c0002t0009g0150 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.903-1299A>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119213980 | ||||||
chr3:119214022
|
A | G | 200 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(197): Show | 397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.903-1341T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119214022 | ||||||
chr3:119214061
|
C | CA | 10 | a0002c0002t0006g0034a0002c0002t0006g0065a0002c0002t0006g0066others(7): Show | 12 | HG01106.hp1 HG02257.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.903-1381dupT | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119214061 | ||||||
chr3:119214068
|
TAAA | T | 19 | a0001c0005t0010g0055a0002c0002t0004g0004a0002c0002t0004g0016others(16): Show | 38 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(35): Show |
intron_variant | MODIFIER | c.903-1390_903-1388d others(5): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119214068 | ||||||
chr3:119214106
|
G | T | 2 | a0002c0002t0001g0117a0002c0002t0009g0150 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.903-1425C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119214106 | ||||||
chr3:119214140
|
T | C | 29 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0021others(26): Show | 69 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.903-1459A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119214140 | ||||||
chr3:119214221
|
A | G | 31 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0021others(28): Show | 71 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.903-1540T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119214221 | ||||||
chr3:119214483
|
A | G | 1 | a0001c0003t0002g0209 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.902+1757T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119214483 | ||||||
chr3:119214494
|
G | A | 1 | a0001c0003t0002g0052 | 2 | NA18989.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.902+1746C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119214494 | ||||||
chr3:119214512
|
G | T | 1 | a0002c0002t0006g0065 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.902+1728C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119214512 | ||||||
chr3:119214517
|
C | T | 31 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0021others(28): Show | 71 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.902+1723G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119214517 | ||||||
chr3:119214719
|
T | G | 1 | a0002c0002t0001g0117 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.902+1521A>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119214719 | ||||||
chr3:119214720
|
G | T | 1 | a0002c0002t0001g0117 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.902+1520C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119214720 | ||||||
chr3:119214800
|
C | T | 1 | a0001c0001t0003g0166 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.902+1440G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119214800 | ||||||
chr3:119214900
|
A | G | 4 | a0001c0001t0003g0018a0001c0001t0003g0041a0001c0001t0003g0146others(1): Show | 8 | HG00639.hp1 HG01123.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.902+1340T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119214900 | ||||||
chr3:119214905
|
G | A | 1 | a0001c0001t0001g0023 | 3 | HG02809.hp2 HG03540.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.902+1335C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119214905 | ||||||
chr3:119215228
|
G | T | 2 | a0001c0001t0001g0023a0001c0001t0001g0097 | 4 | HG02809.hp2 HG03516.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.902+1012C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119215228 | ||||||
chr3:119215381
|
A | G | 200 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(197): Show | 397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.902+859T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119215381 | ||||||
chr3:119215454
|
C | A | 1 | a0001c0003t0002g0208 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.902+786G>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119215454 | ||||||
chr3:119215703
|
T | C | 1 | a0001c0001t0003g0179 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.902+537A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119215703 | ||||||
chr3:119215752
|
G | A | 5 | a0001c0001t0001g0068a0001c0001t0001g0099a0001c0001t0001g0100others(2): Show | 5 | HG03130.hp1 HG03209.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.902+488C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119215752 | ||||||
chr3:119215777
|
T | A | 1 | a0002c0002t0004g0198 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.902+463A>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119215777 | ||||||
chr3:119216167
|
G | A | 2 | a0002c0002t0006g0067a0002c0002t0006g0070 | 2 | HG01106.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.902+73C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119216167 | ||||||
chr3:119216183
|
T | C | 1 | a0001c0001t0002g0122 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.902+57A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119216183 | ||||||
chr3:119216214
|
G | A | 1 | a0002c0002t0008g0098 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.902+26C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119216214 | ||||||
chr3:119216369
|
T | A | 23 | a0001c0001t0002g0106a0001c0001t0002g0191a0001c0001t0003g0044others(20): Show | 55 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.798-25A>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119216369 | ||||||
chr3:119216429
|
TACACACA others(11): Show |
T | 1 | a0002c0002t0001g0082 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.798-103_798-86delG others(17): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119216429 | ||||||
chr3:119216431
|
C | T | 29 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0021others(26): Show | 69 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.798-87G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119216431 | ||||||
chr3:119216431
|
CACACACA others(7): Show |
C | 4 | a0002c0002t0001g0083a0002c0002t0008g0026a0002c0002t0008g0098others(1): Show | 6 | HG01884.hp1 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.798-101_798-88delA others(13): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119216431 | ||||||
chr3:119216433
|
CACACACG others(5): Show |
C | 36 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0021others(33): Show | 78 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.798-101_798-90delA others(11): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119216433 | ||||||
chr3:119216435
|
CACACGCA others(3): Show |
C | 20 | a0001c0001t0001g0099a0002c0002t0004g0004a0002c0002t0004g0016others(17): Show | 38 | HG00423.hp2 HG00639.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.798-101_798-92delA others(9): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119216435 | ||||||
chr3:119216437
|
CACGCACA others(1): Show |
C | 151 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(148): Show | 290 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.798-101_798-94delA others(7): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119216437 | ||||||
chr3:119216439
|
CGCACAT | C | 7 | a0001c0001t0001g0101a0001c0001t0003g0018a0001c0001t0003g0041others(4): Show | 11 | HG00639.hp1 HG01123.hp2 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.798-101_798-96delA others(5): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119216439 | ||||||
chr3:119216445
|
TACACACA others(1): Show |
T | 2 | a0001c0001t0001g0023a0001c0001t0001g0097 | 4 | HG02809.hp2 HG03516.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.798-109_798-102del others(8): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119216445 | ||||||
chr3:119216449
|
C | T | 1 | a0002c0002t0001g0082 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.798-105G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119216449 | ||||||
chr3:119216451
|
C | T | 5 | a0001c0001t0001g0101a0001c0001t0003g0018a0001c0001t0003g0041others(2): Show | 9 | HG00639.hp1 HG01123.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.798-107G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119216451 | ||||||
chr3:119216453
|
C | T | 144 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(141): Show | 276 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.798-109G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119216453 | ||||||
chr3:119216455
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.798-111G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119216455 | ||||||
chr3:119216558
|
C | T | 31 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0021others(28): Show | 71 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.798-214G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119216558 | ||||||
chr3:119216565
|
C | T | 1 | a0001c0001t0001g0118 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.798-221G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119216565 | ||||||
chr3:119217002
|
C | T | 1 | a0001c0001t0001g0141 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.798-658G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217002 | ||||||
chr3:119217003
|
G | A | 1 | a0002c0002t0004g0198 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.798-659C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217003 | ||||||
chr3:119217152
|
A | G | 68 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(65): Show | 140 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.798-808T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217152 | ||||||
chr3:119217176
|
A | G | 2 | a0001c0001t0001g0023a0001c0001t0001g0097 | 4 | HG02809.hp2 HG03516.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.798-832T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217176 | ||||||
chr3:119217225
|
A | G | 221 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(218): Show | 428 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(425): Show |
intron_variant | MODIFIER | c.798-881T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217225 | ||||||
chr3:119217294
|
C | CT | 29 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0021others(26): Show | 69 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.798-951dupA | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217294 | ||||||
chr3:119217367
|
C | T | 2 | a0002c0002t0001g0117a0002c0002t0009g0150 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.798-1023G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217367 | ||||||
chr3:119217454
|
A | T | 28 | a0001c0001t0002g0203a0001c0003t0002g0001a0001c0003t0002g0007others(25): Show | 80 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.798-1110T>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217454 | ||||||
chr3:119217479
|
C | A | 29 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0021others(26): Show | 69 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.798-1135G>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217479 | ||||||
chr3:119217495
|
C | A | 40 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(37): Show | 60 | HG00673.hp2 HG01109.hp1 HG01168.hp2 others(57): Show |
intron_variant | MODIFIER | c.798-1151G>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217495 | ||||||
chr3:119217497
|
A | G | 1 | a0001c0001t0003g0153 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.797+1153T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217497 | ||||||
chr3:119217516
|
C | A | 1 | a0001c0001t0001g0118 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.797+1134G>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217516 | ||||||
chr3:119217544
|
A | G | 21 | a0002c0002t0005g0012a0002c0002t0005g0031a0002c0002t0005g0063others(18): Show | 31 | HG00735.hp1 HG01070.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.797+1106T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217544 | ||||||
chr3:119217643
|
T | C | 1 | a0001c0001t0001g0142 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.797+1007A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217643 | ||||||
chr3:119217659
|
G | C | 1 | a0001c0009t0002g0096 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.797+991C>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217659 | ||||||
chr3:119217716
|
G | A | 2 | a0001c0001t0003g0170a0001c0001t0014g0046 | 3 | HG02055.hp1 HG02809.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.797+934C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217716 | ||||||
chr3:119217735
|
C | T | 3 | a0002c0002t0001g0117a0002c0002t0004g0072a0002c0002t0009g0150 | 3 | HG02258.hp2 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.797+915G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217735 | ||||||
chr3:119217784
|
G | A | 1 | a0001c0001t0002g0025 | 3 | HG00140.hp2 HG00642.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.797+866C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217784 | ||||||
chr3:119217792
|
G | A | 1 | a0001c0001t0003g0182 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.797+858C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217792 | ||||||
chr3:119217828
|
G | A | 28 | a0001c0001t0002g0203a0001c0003t0002g0001a0001c0003t0002g0007others(25): Show | 80 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.797+822C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217828 | ||||||
chr3:119217842
|
CA | C | 63 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(60): Show | 145 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.797+807delT | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217842 | ||||||
chr3:119217842
|
CAA | C | 99 | a0001c0001t0001g0110a0001c0001t0001g0140a0001c0001t0002g0006others(96): Show | 173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.797+806_797+807del others(2): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217842 | ||||||
chr3:119217842
|
CAAAAA | C | 26 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0021others(23): Show | 65 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.797+803_797+807del others(5): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217842 | ||||||
chr3:119217861
|
A | G | 11 | a0002c0002t0005g0012a0002c0002t0005g0031a0002c0002t0005g0063others(8): Show | 19 | HG00735.hp1 HG01070.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.797+789T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217861 | ||||||
chr3:119218167
|
C | T | 221 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(218): Show | 428 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(425): Show |
intron_variant | MODIFIER | c.797+483G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119218167 | ||||||
chr3:119218178
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.797+472C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119218178 | ||||||
chr3:119218194
|
G | A | 2 | a0001c0001t0003g0028a0001c0001t0003g0144 | 4 | HG00544.hp1 HG02132.hp2 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.797+456C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119218194 | ||||||
chr3:119218280
|
T | C | 10 | a0002c0002t0006g0034a0002c0002t0006g0065a0002c0002t0006g0066others(7): Show | 12 | HG01106.hp1 HG02257.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.797+370A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119218280 | ||||||
chr3:119218490
|
G | A | 6 | a0001c0001t0001g0015a0001c0001t0001g0095a0001c0001t0001g0135others(3): Show | 10 | HG01109.hp1 HG01496.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.797+160C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119218490 | ||||||
chr3:119218606
|
C | G | 3 | a0001c0001t0001g0023a0001c0001t0001g0097a0002c0002t0001g0117 | 5 | HG02258.hp2 HG02809.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.797+44G>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119218606 | ||||||
chr3:119218919
|
C | T | 3 | a0002c0002t0004g0016a0002c0002t0004g0184a0002c0002t0004g0199 | 7 | HG00423.hp2 NA18747.hp1 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.675-147G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119218919 | ||||||
chr3:119219198
|
T | C | 2 | a0001c0001t0001g0023a0001c0001t0001g0097 | 4 | HG02809.hp2 HG03516.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.675-426A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119219198 | ||||||
chr3:119219272
|
T | C | 81 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0053others(78): Show | 145 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.675-500A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119219272 | ||||||
chr3:119219470
|
A | T | 1 | a0001c0001t0003g0152 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.675-698T>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119219470 | ||||||
chr3:119219643
|
A | T | 1 | a0001c0001t0003g0043 | 2 | NA18998.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.675-871T>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119219643 | ||||||
chr3:119219727
|
G | A | 2 | a0002c0002t0001g0060a0002c0002t0001g0085 | 2 | HG02735.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.675-955C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119219727 | ||||||
chr3:119219769
|
T | C | 3 | a0001c0004t0001g0030a0001c0004t0001g0091a0002c0002t0004g0196 | 4 | HG01884.hp2 HG02572.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.675-997A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119219769 | ||||||
chr3:119219774
|
A | G | 32 | a0001c0001t0002g0164a0002c0002t0001g0002a0002c0002t0001g0008others(29): Show | 72 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.675-1002T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119219774 | ||||||
chr3:119219974
|
C | A | 1 | a0001c0001t0001g0137 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.675-1202G>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119219974 | ||||||
chr3:119220175
|
C | CA | 3 | a0001c0001t0003g0017a0001c0003t0002g0186a0002c0002t0004g0199 | 6 | HG03834.hp1 NA18986.hp2 NA18988.hp2 others(3): Show |
intron_variant | MODIFIER | c.675-1404dupT | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119220175 | ||||||
chr3:119220256
|
T | C | 1 | a0001c0009t0002g0096 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.675-1484A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119220256 | ||||||
chr3:119220386
|
T | C | 1 | a0001c0003t0002g0210 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.675-1614A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119220386 | ||||||
chr3:119220421
|
A | C | 1 | a0001c0001t0007g0190 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.675-1649T>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119220421 | ||||||
chr3:119220439
|
C | T | 3 | a0002c0002t0008g0026a0002c0002t0008g0098a0002c0002t0008g0134 | 5 | HG01884.hp1 HG02486.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.675-1667G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119220439 | ||||||
chr3:119220440
|
G | A | 1 | a0002c0002t0006g0071 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.675-1668C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119220440 | ||||||
chr3:119220442
|
G | A | 1 | a0001c0001t0003g0170 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.675-1670C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119220442 | ||||||
chr3:119220533
|
A | G | 32 | a0001c0001t0002g0164a0002c0002t0001g0002a0002c0002t0001g0008others(29): Show | 72 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.675-1761T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119220533 | ||||||
chr3:119220632
|
C | T | 4 | a0001c0003t0002g0051a0001c0003t0002g0211a0001c0003t0002g0213others(1): Show | 5 | HG02080.hp1 HG02155.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.675-1860G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119220632 | ||||||
chr3:119220634
|
G | A | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | HG01168.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.675-1862C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119220634 | ||||||
chr3:119220636
|
C | T | 1 | a0001c0001t0003g0159 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.675-1864G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119220636 | ||||||
chr3:119220729
|
G | T | 40 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(37): Show | 60 | HG00673.hp2 HG01109.hp1 HG01168.hp2 others(57): Show |
intron_variant | MODIFIER | c.675-1957C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119220729 | ||||||
chr3:119220761
|
C | A | 40 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(37): Show | 60 | HG00673.hp2 HG01109.hp1 HG01168.hp2 others(57): Show |
intron_variant | MODIFIER | c.675-1989G>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119220761 | ||||||
chr3:119220765
|
T | C | 2 | a0002c0002t0001g0022a0002c0002t0001g0074 | 4 | NA18969.hp1 NA18980.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.675-1993A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119220765 | ||||||
chr3:119220782
|
C | G | 1 | a0001c0001t0002g0120 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.675-2010G>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119220782 | ||||||
chr3:119220880
|
G | A | 11 | a0002c0002t0005g0012a0002c0002t0005g0031a0002c0002t0005g0063others(8): Show | 19 | HG00735.hp1 HG01070.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.675-2108C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119220880 | ||||||
chr3:119220942
|
C | T | 3 | a0001c0004t0001g0030a0001c0004t0001g0091a0002c0002t0004g0196 | 4 | HG01884.hp2 HG02572.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.675-2170G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119220942 | ||||||
chr3:119220985
|
C | CA | 30 | a0001c0001t0001g0132a0001c0001t0002g0126a0002c0002t0001g0002others(27): Show | 69 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.675-2214dupT | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119220985 | ||||||
chr3:119221220
|
T | C | 2 | a0001c0001t0003g0017a0001c0003t0002g0186 | 5 | HG03834.hp1 NA18986.hp2 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.675-2448A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119221220 | ||||||
chr3:119221253
|
G | A | 3 | a0001c0001t0002g0164a0002c0002t0001g0117a0002c0002t0009g0150 | 3 | HG02258.hp2 HG02451.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.675-2481C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119221253 | ||||||
chr3:119221295
|
T | G | 3 | a0001c0004t0001g0030a0001c0004t0001g0091a0002c0002t0004g0196 | 4 | HG01884.hp2 HG02572.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.675-2523A>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119221295 | ||||||
chr3:119221355
|
A | C | 11 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0053others(8): Show | 28 | HG00408.hp1 HG02083.hp2 HG02129.hp1 others(25): Show |
intron_variant | MODIFIER | c.675-2583T>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119221355 | ||||||
chr3:119221467
|
C | T | 69 | a0001c0001t0002g0006a0001c0001t0002g0013a0001c0001t0002g0025others(66): Show | 116 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.674+2591G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119221467 | ||||||
chr3:119221536
|
C | T | 17 | a0002c0002t0004g0004a0002c0002t0004g0016a0002c0002t0004g0020others(14): Show | 36 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(33): Show |
intron_variant | MODIFIER | c.674+2522G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119221536 | ||||||
chr3:119221553
|
A | G | 70 | a0001c0001t0002g0164a0002c0002t0001g0002a0002c0002t0001g0008others(67): Show | 139 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.674+2505T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119221553 | ||||||
chr3:119221564
|
A | G | 2 | a0002c0002t0001g0080a0002c0002t0001g0081 | 2 | HG01943.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.674+2494T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119221564 | ||||||
chr3:119221736
|
C | A | 2 | a0001c0001t0003g0166a0001c0001t0003g0167 | 2 | HG01099.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.674+2322G>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119221736 | ||||||
chr3:119221782
|
C | T | 1 | a0001c0001t0001g0118 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.674+2276G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119221782 | ||||||
chr3:119221834
|
T | C | 1 | a0002c0002t0004g0049 | 2 | NA18982.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.674+2224A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119221834 | ||||||
chr3:119221914
|
A | G | 1 | a0001c0001t0001g0023 | 3 | HG02809.hp2 HG03540.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.674+2144T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119221914 | ||||||
chr3:119222009
|
G | C | 1 | a0001c0001t0018g0073 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.674+2049C>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222009 | ||||||
chr3:119222056
|
T | C | 2 | a0001c0001t0002g0108a0001c0001t0002g0109 | 2 | HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.674+2002A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222056 | ||||||
chr3:119222182
|
T | G | 41 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(38): Show | 61 | HG00673.hp2 HG01109.hp1 HG01168.hp2 others(58): Show |
intron_variant | MODIFIER | c.674+1876A>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222182 | ||||||
chr3:119222251
|
G | A | 193 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(190): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.674+1807C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222251 | ||||||
chr3:119222388
|
A | G | 31 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0021others(28): Show | 71 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.674+1670T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222388 | ||||||
chr3:119222419
|
G | GGC | 80 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0053others(77): Show | 144 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.674+1638_674+1639i others(4): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222419 | ||||||
chr3:119222421
|
A | G | 80 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0053others(77): Show | 144 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.674+1637T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222421 | ||||||
chr3:119222422
|
T | G | 80 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0053others(77): Show | 144 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.674+1636A>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222422 | ||||||
chr3:119222423
|
C | G | 80 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0053others(77): Show | 144 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.674+1635G>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222423 | ||||||
chr3:119222428
|
GC | G | 80 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0053others(77): Show | 144 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.674+1629delG | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222428 | ||||||
chr3:119222525
|
T | G | 1 | a0001c0001t0003g0174 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.674+1533A>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222525 | ||||||
chr3:119222540
|
C | G | 18 | a0002c0002t0004g0004a0002c0002t0004g0016a0002c0002t0004g0020others(15): Show | 37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.674+1518G>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222540 | ||||||
chr3:119222577
|
C | T | 1 | a0001c0001t0002g0121 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.674+1481G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222577 | ||||||
chr3:119222594
|
A | G | 191 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(188): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.674+1464T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222594 | ||||||
chr3:119222690
|
T | C | 17 | a0002c0002t0005g0012a0002c0002t0005g0031a0002c0002t0005g0063others(14): Show | 26 | HG00735.hp1 HG01070.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.674+1368A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222690 | ||||||
chr3:119222708
|
T | G | 2 | a0001c0003t0009g0180a0001c0003t0009g0217 | 2 | NA19074.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.674+1350A>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222708 | ||||||
chr3:119222787
|
T | G | 9 | a0001c0001t0002g0025a0001c0001t0002g0039a0001c0001t0002g0104others(6): Show | 12 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(9): Show |
intron_variant | MODIFIER | c.674+1271A>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222787 | ||||||
chr3:119222845
|
C | G | 8 | a0002c0002t0005g0012a0002c0002t0005g0031a0002c0002t0005g0063others(5): Show | 14 | HG00735.hp1 HG01070.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.674+1213G>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222845 | ||||||
chr3:119222895
|
G | T | 193 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(190): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.674+1163C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222895 | ||||||
chr3:119222902
|
A | G | 31 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0021others(28): Show | 71 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.674+1156T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222902 | ||||||
chr3:119222985
|
A | G | 70 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0021others(67): Show | 139 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.674+1073T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222985 | ||||||
chr3:119223040
|
T | C | 1 | a0002c0002t0008g0134 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.674+1018A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119223040 | ||||||
chr3:119223045
|
T | C | 31 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0024others(28): Show | 46 | HG00673.hp2 HG01109.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.674+1013A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119223045 | ||||||
chr3:119223289
|
A | C | 2 | a0002c0002t0001g0117a0002c0002t0009g0150 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.674+769T>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119223289 | ||||||
chr3:119223378
|
T | C | 29 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0021others(26): Show | 69 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.674+680A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119223378 | ||||||
chr3:119223412
|
T | C | 11 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0053others(8): Show | 28 | HG00408.hp1 HG02083.hp2 HG02129.hp1 others(25): Show |
intron_variant | MODIFIER | c.674+646A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119223412 | ||||||
chr3:119223437
|
G | A | 1 | a0001c0001t0001g0037 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.674+621C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119223437 | ||||||
chr3:119223628
|
C | T | 18 | a0002c0002t0004g0004a0002c0002t0004g0016a0002c0002t0004g0020others(15): Show | 37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.674+430G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119223628 | ||||||
chr3:119223697
|
GC | G | 80 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0053others(77): Show | 144 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.674+360delG | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119223697 | ||||||
chr3:119223792
|
G | A | 1 | a0001c0001t0003g0156 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.674+266C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119223792 | ||||||
chr3:119223862
|
T | G | 9 | a0001c0001t0002g0025a0001c0001t0002g0039a0001c0001t0002g0104others(6): Show | 12 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(9): Show |
intron_variant | MODIFIER | c.674+196A>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119223862 | ||||||
chr3:119223868
|
G | A | 2 | a0002c0002t0001g0117a0002c0002t0009g0150 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.674+190C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119223868 | ||||||
chr3:119223973
|
G | A | 1 | a0001c0003t0002g0206 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.674+85C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119223973 | ||||||
chr3:119223974
|
A | G | 1 | a0001c0003t0002g0206 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.674+84T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119223974 | ||||||
chr3:119224307
|
C | T | 1 | a0001c0003t0002g0205 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.487-62G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119224307 | ||||||
chr3:119224338
|
T | C | 2 | a0001c0004t0001g0030a0001c0004t0001g0091 | 3 | HG01884.hp2 HG02572.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.487-93A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119224338 | ||||||
chr3:119224372
|
T | C | 1 | a0002c0002t0006g0034 | 2 | HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.487-127A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119224372 | ||||||
chr3:119224387
|
G | A | 29 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0021others(26): Show | 69 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.487-142C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119224387 | ||||||
chr3:119224387
|
G | C | 1 | a0001c0001t0003g0149 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.487-142C>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119224387 | ||||||
chr3:119224434
|
T | A | 1 | a0001c0001t0003g0175 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.487-189A>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119224434 | ||||||
chr3:119224454
|
G | A | 2 | a0001c0001t0001g0036a0001c0001t0001g0037 | 4 | HG01255.hp1 HG01256.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.487-209C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119224454 | ||||||
chr3:119224485
|
C | G | 221 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(218): Show | 428 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(425): Show |
intron_variant | MODIFIER | c.487-240G>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119224485 | ||||||
chr3:119224557
|
C | T | 8 | a0002c0002t0005g0012a0002c0002t0005g0031a0002c0002t0005g0063others(5): Show | 14 | HG00735.hp1 HG01070.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.487-312G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119224557 | ||||||
chr3:119224563
|
T | G | 29 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0021others(26): Show | 69 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.487-318A>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119224563 | ||||||
chr3:119224595
|
T | C | 11 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0053others(8): Show | 28 | HG00408.hp1 HG02083.hp2 HG02129.hp1 others(25): Show |
intron_variant | MODIFIER | c.487-350A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119224595 | ||||||
chr3:119224638
|
C | T | 1 | a0001c0003t0002g0204 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.487-393G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119224638 | ||||||
chr3:119224705
|
A | G | 190 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(187): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.487-460T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119224705 | ||||||
chr3:119224773
|
A | G | 11 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0053others(8): Show | 28 | HG00408.hp1 HG02083.hp2 HG02129.hp1 others(25): Show |
intron_variant | MODIFIER | c.487-528T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119224773 | ||||||
chr3:119225052
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.487-807A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119225052 | ||||||
chr3:119225063
|
A | G | 193 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(190): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.487-818T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119225063 | ||||||
chr3:119225302
|
T | C | 1 | a0001c0001t0002g0123 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.487-1057A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119225302 | ||||||
chr3:119225428
|
G | A | 3 | a0001c0003t0002g0211a0001c0004t0001g0030a0001c0004t0001g0091 | 4 | HG01884.hp2 HG02155.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.487-1183C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119225428 | ||||||
chr3:119225482
|
C | T | 2 | a0002c0002t0001g0117a0002c0002t0009g0150 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.487-1237G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119225482 | ||||||
chr3:119225563
|
AT | A | 121 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0023others(118): Show | 216 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.486+1245delA | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119225563 | ||||||
chr3:119225570
|
T | G | 29 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0021others(26): Show | 69 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.486+1239A>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119225570 | ||||||
chr3:119225618
|
A | G | 1 | a0001c0001t0002g0104 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.486+1191T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119225618 | ||||||
chr3:119225648
|
C | A | 29 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0021others(26): Show | 69 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.486+1161G>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119225648 | ||||||
chr3:119225649
|
A | G | 31 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0021others(28): Show | 71 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.486+1160T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119225649 | ||||||
chr3:119225658
|
T | A | 221 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(218): Show | 428 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(425): Show |
intron_variant | MODIFIER | c.486+1151A>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119225658 | ||||||
chr3:119225777
|
G | A | 1 | a0001c0001t0003g0158 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.486+1032C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119225777 | ||||||
chr3:119225897
|
CTATA | C | 18 | a0002c0002t0004g0004a0002c0002t0004g0016a0002c0002t0004g0020others(15): Show | 37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.486+908_486+911del others(4): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119225897 | ||||||
chr3:119225901
|
A | G | 2 | a0002c0002t0008g0026a0002c0002t0008g0134 | 4 | HG01884.hp1 HG02486.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.486+908T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119225901 | ||||||
chr3:119225986
|
T | C | 1 | a0001c0001t0018g0073 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.486+823A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119225986 | ||||||
chr3:119225990
|
A | G | 1 | a0002c0002t0004g0187 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.486+819T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119225990 | ||||||
chr3:119226103
|
C | T | 31 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0021others(28): Show | 71 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.486+706G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119226103 | ||||||
chr3:119226123
|
GA | G | 39 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(36): Show | 59 | HG00673.hp2 HG01109.hp1 HG01168.hp2 others(56): Show |
intron_variant | MODIFIER | c.486+685delT | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119226123 | ||||||
chr3:119226281
|
G | A | 31 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0021others(28): Show | 71 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.486+528C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119226281 | ||||||
chr3:119226309
|
T | C | 1 | a0001c0001t0002g0114 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.486+500A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119226309 | ||||||
chr3:119226312
|
T | C | 193 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(190): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.486+497A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119226312 | ||||||
chr3:119226498
|
A | T | 1 | a0002c0002t0004g0192 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.486+311T>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119226498 | ||||||
chr3:119226522
|
C | T | 2 | a0002c0002t0001g0117a0002c0002t0009g0150 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.486+287G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119226522 | ||||||
chr3:119226605
|
A | G | 1 | a0001c0001t0002g0164 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.486+204T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119226605 | ||||||
chr3:119226731
|
T | C | 31 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0021others(28): Show | 71 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.486+78A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119226731 | ||||||
chr3:119226767
|
G | A | 31 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0021others(28): Show | 71 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.486+42C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119226767 | ||||||
chr3:119226776
|
C | G | 2 | a0001c0004t0001g0030a0001c0004t0001g0091 | 3 | HG01884.hp2 HG02572.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.486+33G>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119226776 | ||||||
chr3:119227341
|
G | A | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.254-300C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119227341 | ||||||
chr3:119227354
|
G | A | 1 | a0002c0002t0001g0086 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.254-313C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119227354 | ||||||
chr3:119227476
|
G | A | 9 | a0001c0001t0001g0014a0001c0001t0001g0128a0001c0001t0001g0131others(6): Show | 14 | HG01433.hp2 HG01884.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.254-435C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119227476 | ||||||
chr3:119227699
|
T | C | 31 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0021others(28): Show | 71 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.254-658A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119227699 | ||||||
chr3:119227810
|
G | A | 1 | a0001c0001t0002g0124 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.254-769C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119227810 | ||||||
chr3:119227839
|
C | T | 2 | a0002c0002t0001g0117a0002c0002t0009g0150 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.254-798G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119227839 | ||||||
chr3:119227904
|
C | T | 31 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0021others(28): Show | 71 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.254-863G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119227904 | ||||||
chr3:119227909
|
G | A | 1 | a0001c0001t0003g0157 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.254-868C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119227909 | ||||||
chr3:119227950
|
G | A | 19 | a0001c0001t0003g0147a0001c0001t0003g0163a0002c0002t0005g0012others(16): Show | 28 | HG00735.hp1 HG01070.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.254-909C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119227950 | ||||||
chr3:119227982
|
A | G | 29 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0021others(26): Show | 69 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.254-941T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119227982 | ||||||
chr3:119228206
|
G | A | 1 | a0002c0002t0004g0193 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.254-1165C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228206 | ||||||
chr3:119228223
|
C | T | 1 | a0001c0001t0018g0073 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.254-1182G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228223 | ||||||
chr3:119228284
|
G | A | 2 | a0002c0002t0001g0086a0002c0002t0001g0093 | 2 | HG01255.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.254-1243C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228284 | ||||||
chr3:119228301
|
C | A | 64 | a0001c0001t0002g0006a0001c0001t0002g0013a0001c0001t0002g0025others(61): Show | 111 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.254-1260G>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228301 | ||||||
chr3:119228421
|
T | C | 29 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0021others(26): Show | 69 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.254-1380A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228421 | ||||||
chr3:119228461
|
T | C | 1 | a0001c0001t0018g0073 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.253+1386A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228461 | ||||||
chr3:119228499
|
G | A | 2 | a0001c0001t0003g0170a0001c0001t0014g0046 | 3 | HG02055.hp1 HG02809.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.253+1348C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228499 | ||||||
chr3:119228791
|
A | C | 18 | a0002c0002t0004g0004a0002c0002t0004g0016a0002c0002t0004g0020others(15): Show | 37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1056T>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228791 | ||||||
chr3:119228792
|
A | T | 18 | a0002c0002t0004g0004a0002c0002t0004g0016a0002c0002t0004g0020others(15): Show | 37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1055T>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228792 | ||||||
chr3:119228793
|
G | A | 18 | a0002c0002t0004g0004a0002c0002t0004g0016a0002c0002t0004g0020others(15): Show | 37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1054C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228793 | ||||||
chr3:119228794
|
G | T | 18 | a0002c0002t0004g0004a0002c0002t0004g0016a0002c0002t0004g0020others(15): Show | 37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1053C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228794 | ||||||
chr3:119228795
|
G | C | 18 | a0002c0002t0004g0004a0002c0002t0004g0016a0002c0002t0004g0020others(15): Show | 37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1052C>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228795 | ||||||
chr3:119228797
|
G | A | 18 | a0002c0002t0004g0004a0002c0002t0004g0016a0002c0002t0004g0020others(15): Show | 37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1050C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228797 | ||||||
chr3:119228798
|
G | T | 18 | a0002c0002t0004g0004a0002c0002t0004g0016a0002c0002t0004g0020others(15): Show | 37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1049C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228798 | ||||||
chr3:119228799
|
A | C | 18 | a0002c0002t0004g0004a0002c0002t0004g0016a0002c0002t0004g0020others(15): Show | 37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1048T>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228799 | ||||||
chr3:119228800
|
G | T | 18 | a0002c0002t0004g0004a0002c0002t0004g0016a0002c0002t0004g0020others(15): Show | 37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1047C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228800 | ||||||
chr3:119228804
|
C | T | 18 | a0002c0002t0004g0004a0002c0002t0004g0016a0002c0002t0004g0020others(15): Show | 37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1043G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228804 | ||||||
chr3:119228805
|
CAGG | C | 18 | a0002c0002t0004g0004a0002c0002t0004g0016a0002c0002t0004g0020others(15): Show | 37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1039_253+1041d others(5): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228805 | ||||||
chr3:119228810
|
G | A | 1 | a0001c0001t0003g0177 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.253+1037C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228810 | ||||||
chr3:119228810
|
G | T | 18 | a0002c0002t0004g0004a0002c0002t0004g0016a0002c0002t0004g0020others(15): Show | 37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1037C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228810 | ||||||
chr3:119228811
|
G | T | 18 | a0002c0002t0004g0004a0002c0002t0004g0016a0002c0002t0004g0020others(15): Show | 37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1036C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228811 | ||||||
chr3:119228812
|
G | C | 18 | a0002c0002t0004g0004a0002c0002t0004g0016a0002c0002t0004g0020others(15): Show | 37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1035C>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228812 | ||||||
chr3:119228813
|
A | G | 4 | a0001c0001t0002g0013a0001c0001t0002g0125a0001c0001t0002g0126others(1): Show | 8 | HG00609.hp2 HG02056.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.253+1034T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228813 | ||||||
chr3:119228813
|
A | T | 18 | a0002c0002t0004g0004a0002c0002t0004g0016a0002c0002t0004g0020others(15): Show | 37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1034T>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228813 | ||||||
chr3:119228814
|
T | A | 18 | a0002c0002t0004g0004a0002c0002t0004g0016a0002c0002t0004g0020others(15): Show | 37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1033A>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228814 | ||||||
chr3:119228816
|
A | C | 18 | a0002c0002t0004g0004a0002c0002t0004g0016a0002c0002t0004g0020others(15): Show | 37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1031T>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228816 | ||||||
chr3:119228817
|
A | T | 18 | a0002c0002t0004g0004a0002c0002t0004g0016a0002c0002t0004g0020others(15): Show | 37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1030T>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228817 | ||||||
chr3:119228819
|
G | T | 18 | a0002c0002t0004g0004a0002c0002t0004g0016a0002c0002t0004g0020others(15): Show | 37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1028C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228819 | ||||||
chr3:119228821
|
A | T | 18 | a0002c0002t0004g0004a0002c0002t0004g0016a0002c0002t0004g0020others(15): Show | 37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1026T>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228821 | ||||||
chr3:119228823
|
T | TG | 18 | a0002c0002t0004g0004a0002c0002t0004g0016a0002c0002t0004g0020others(15): Show | 37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1023_253+1024i others(3): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228823 | ||||||
chr3:119228825
|
A | C | 18 | a0002c0002t0004g0004a0002c0002t0004g0016a0002c0002t0004g0020others(15): Show | 37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1022T>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228825 | ||||||
chr3:119228826
|
TAAAAAG | T | 18 | a0002c0002t0004g0004a0002c0002t0004g0016a0002c0002t0004g0020others(15): Show | 37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1015_253+1020d others(8): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228826 | ||||||
chr3:119228833
|
A | T | 18 | a0002c0002t0004g0004a0002c0002t0004g0016a0002c0002t0004g0020others(15): Show | 37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1014T>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228833 | ||||||
chr3:119228834
|
G | T | 18 | a0002c0002t0004g0004a0002c0002t0004g0016a0002c0002t0004g0020others(15): Show | 37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1013C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228834 | ||||||
chr3:119228836
|
A | T | 18 | a0002c0002t0004g0004a0002c0002t0004g0016a0002c0002t0004g0020others(15): Show | 37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1011T>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228836 | ||||||
chr3:119228837
|
A | C | 18 | a0002c0002t0004g0004a0002c0002t0004g0016a0002c0002t0004g0020others(15): Show | 37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1010T>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228837 | ||||||
chr3:119228838
|
G | T | 18 | a0002c0002t0004g0004a0002c0002t0004g0016a0002c0002t0004g0020others(15): Show | 37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1009C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228838 | ||||||
chr3:119228839
|
A | C | 18 | a0002c0002t0004g0004a0002c0002t0004g0016a0002c0002t0004g0020others(15): Show | 37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1008T>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228839 | ||||||
chr3:119228840
|
G | T | 18 | a0002c0002t0004g0004a0002c0002t0004g0016a0002c0002t0004g0020others(15): Show | 37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1007C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228840 | ||||||
chr3:119228841
|
G | C | 18 | a0002c0002t0004g0004a0002c0002t0004g0016a0002c0002t0004g0020others(15): Show | 37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1006C>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228841 | ||||||
chr3:119228843
|
A | C | 18 | a0002c0002t0004g0004a0002c0002t0004g0016a0002c0002t0004g0020others(15): Show | 37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1004T>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228843 | ||||||
chr3:119228844
|
TGAG | T | 18 | a0002c0002t0004g0004a0002c0002t0004g0016a0002c0002t0004g0020others(15): Show | 37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1000_253+1002d others(5): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228844 | ||||||
chr3:119228848
|
A | C | 18 | a0002c0002t0004g0004a0002c0002t0004g0016a0002c0002t0004g0020others(15): Show | 37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+999T>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228848 | ||||||
chr3:119228921
|
C | T | 11 | a0002c0002t0005g0012a0002c0002t0005g0031a0002c0002t0005g0063others(8): Show | 19 | HG00735.hp1 HG01070.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.253+926G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228921 | ||||||
chr3:119229028
|
C | T | 1 | a0001c0001t0002g0212 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.253+819G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119229028 | ||||||
chr3:119229103
|
C | T | 2 | a0002c0002t0001g0117a0002c0002t0009g0150 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.253+744G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119229103 | ||||||
chr3:119229164
|
C | T | 3 | a0001c0001t0003g0176a0001c0001t0003g0177a0001c0001t0003g0185 | 3 | HG02818.hp1 HG02896.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.253+683G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119229164 | ||||||
chr3:119229308
|
C | T | 202 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(199): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.253+539G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119229308 | ||||||
chr3:119229324
|
A | G | 31 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0021others(28): Show | 71 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.253+523T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119229324 | ||||||
chr3:119229409
|
C | A | 75 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0053others(72): Show | 139 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.253+438G>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119229409 | ||||||
chr3:119229441
|
C | T | 183 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(180): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.253+406G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119229441 | ||||||
chr3:119229590
|
G | C | 7 | a0001c0001t0001g0197a0002c0002t0004g0020a0002c0002t0004g0072others(4): Show | 9 | HG00639.hp2 HG01109.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.253+257C>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119229590 | ||||||
chr3:119229654
|
C | A | 1 | a0002c0002t0005g0064 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.253+193G>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119229654 | ||||||
chr3:119229771
|
G | C | 44 | a0001c0001t0001g0023a0001c0001t0001g0097a0001c0001t0002g0164others(41): Show | 99 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.253+76C>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119229771 | ||||||
chr3:119230298
|
G | A | 178 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(175): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.-145-54C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119230298 | ||||||
chr3:119230333
|
C | T | 1 | a0001c0001t0001g0023 | 3 | HG02809.hp2 HG03540.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-145-89G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119230333 | ||||||
chr3:119230378
|
T | C | 3 | a0001c0001t0001g0128a0001c0001t0001g0131a0001c0001t0001g0132 | 3 | HG02965.hp1 HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-145-134A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119230378 | ||||||
chr3:119230387
|
C | G | 11 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0053others(8): Show | 28 | HG00408.hp1 HG02083.hp2 HG02129.hp1 others(25): Show |
intron_variant | MODIFIER | c.-145-143G>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119230387 | ||||||
chr3:119230466
|
C | A | 1 | a0001c0001t0001g0111 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-145-222G>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119230466 | ||||||
chr3:119230500
|
C | T | 8 | a0001c0001t0001g0015a0001c0001t0001g0135a0001c0001t0001g0136others(5): Show | 15 | HG00140.hp2 HG00642.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.-145-256G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119230500 | ||||||
chr3:119230706
|
G | C | 1 | a0002c0002t0001g0088 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-145-462C>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119230706 | ||||||
chr3:119230719
|
A | T | 11 | a0001c0001t0001g0014a0001c0001t0001g0097a0001c0001t0001g0118others(8): Show | 15 | HG01433.hp2 HG01891.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-145-475T>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119230719 | ||||||
chr3:119230721
|
A | G | 7 | a0002c0002t0004g0020a0002c0002t0004g0072a0002c0002t0004g0079others(4): Show | 9 | HG00639.hp2 HG01106.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-145-477T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119230721 | ||||||
chr3:119230937
|
G | A | 11 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0053others(8): Show | 28 | HG00408.hp1 HG02083.hp2 HG02129.hp1 others(25): Show |
intron_variant | MODIFIER | c.-145-693C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119230937 | ||||||
chr3:119231165
|
T | G | 2 | a0001c0005t0010g0035a0001c0005t0010g0055 | 3 | HG03041.hp2 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-145-921A>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119231165 | ||||||
chr3:119231263
|
G | A | 1 | a0001c0001t0001g0068 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-145-1019C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119231263 | ||||||
chr3:119231333
|
G | A | 1 | a0001c0001t0002g0125 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-145-1089C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119231333 | ||||||
chr3:119231398
|
G | A | 1 | a0002c0002t0015g0119 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-145-1154C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119231398 | ||||||
chr3:119231441
|
A | G | 39 | a0001c0001t0018g0073a0002c0002t0001g0002a0002c0002t0001g0008others(36): Show | 86 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-145-1197T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119231441 | ||||||
chr3:119231652
|
G | A | 59 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0036others(56): Show | 117 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.-145-1408C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119231652 | ||||||
chr3:119231658
|
C | A | 117 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0014others(114): Show | 198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.-145-1414G>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119231658 | ||||||
chr3:119231667
|
G | A | 1 | a0001c0001t0018g0073 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-145-1423C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119231667 | ||||||
chr3:119231749
|
T | A | 2 | a0001c0001t0001g0097a0001c0001t0001g0118 | 2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-145-1505A>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119231749 | ||||||
chr3:119231750
|
T | A | 2 | a0001c0001t0001g0097a0001c0001t0001g0118 | 2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-145-1506A>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119231750 | ||||||
chr3:119231751
|
T | A | 2 | a0001c0001t0001g0097a0001c0001t0001g0118 | 2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-145-1507A>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119231751 | ||||||
chr3:119231762
|
TTTTA | T | 8 | a0001c0001t0001g0015a0001c0001t0001g0135a0001c0001t0001g0136others(5): Show | 15 | HG00140.hp2 HG00642.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.-145-1522_-145-151 others(8): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119231762 | ||||||
chr3:119231791
|
T | TTATAAAA | 141 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(138): Show | 236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.-145-1554_-145-154 others(11): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119231791 | ||||||
chr3:119231801
|
TA | T | 7 | a0001c0001t0001g0014a0001c0001t0001g0128a0001c0001t0001g0131others(4): Show | 11 | HG01433.hp2 HG02055.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-145-1558delT | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119231801 | ||||||
chr3:119231804
|
A | T | 7 | a0001c0001t0001g0014a0001c0001t0001g0128a0001c0001t0001g0131others(4): Show | 11 | HG01433.hp2 HG02055.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-145-1560T>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119231804 | ||||||
chr3:119231806
|
T | TATAA | 28 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0021others(25): Show | 68 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.-145-1563_-145-156 others(8): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119231806 | ||||||
chr3:119231807
|
A | T | 7 | a0001c0001t0001g0014a0001c0001t0001g0128a0001c0001t0001g0131others(4): Show | 11 | HG01433.hp2 HG02055.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-145-1563T>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119231807 | ||||||
chr3:119231808
|
A | T | 7 | a0001c0001t0001g0014a0001c0001t0001g0128a0001c0001t0001g0131others(4): Show | 11 | HG01433.hp2 HG02055.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-145-1564T>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119231808 | ||||||
chr3:119232188
|
A | G | 15 | a0001c0001t0001g0015a0001c0001t0001g0135a0001c0001t0001g0136others(12): Show | 24 | HG00140.hp2 HG00642.hp2 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.-145-1944T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119232188 | ||||||
chr3:119232193
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-145-1949C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119232193 | ||||||
chr3:119232550
|
T | A | 8 | a0001c0001t0001g0014a0001c0001t0001g0128a0001c0001t0001g0131others(5): Show | 12 | HG01433.hp2 HG01891.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-145-2306A>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119232550 | ||||||
chr3:119232551
|
ATTCAGG | A | 8 | a0001c0001t0001g0014a0001c0001t0001g0128a0001c0001t0001g0131others(5): Show | 12 | HG01433.hp2 HG01891.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-145-2313_-145-230 others(10): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119232551 | ||||||
chr3:119232561
|
C | T | 1 | a0002c0002t0001g0078 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-145-2317G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119232561 | ||||||
chr3:119232568
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-145-2324C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119232568 | ||||||
chr3:119232714
|
T | C | 1 | a0001c0001t0002g0191 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-145-2470A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119232714 | ||||||
chr3:119232864
|
C | T | 2 | a0001c0001t0002g0164a0001c0001t0002g0183 | 2 | HG02451.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-145-2620G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119232864 | ||||||
chr3:119233098
|
G | A | 51 | a0001c0001t0001g0061a0001c0001t0001g0068a0001c0001t0001g0095others(48): Show | 101 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.-145-2854C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119233098 | ||||||
chr3:119233131
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-145-2887C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119233131 | ||||||
chr3:119233169
|
G | A | 27 | a0001c0001t0002g0203a0001c0001t0002g0212a0001c0003t0002g0001others(24): Show | 78 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.-145-2925C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119233169 | ||||||
chr3:119233246
|
C | T | 1 | a0002c0002t0008g0098 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-145-3002G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119233246 | ||||||
chr3:119233307
|
G | A | 1 | a0001c0001t0003g0158 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-145-3063C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119233307 | ||||||
chr3:119233397
|
T | G | 1 | a0001c0001t0013g0042 | 2 | HG00642.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.-145-3153A>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119233397 | ||||||
chr3:119233401
|
C | T | 1 | a0002c0002t0001g0021 | 3 | NA18956.hp2 NA18968.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.-145-3157G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119233401 | ||||||
chr3:119233600
|
G | T | 1 | a0001c0001t0002g0164 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-146+3253C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119233600 | ||||||
chr3:119233712
|
T | C | 2 | a0001c0001t0001g0097a0001c0001t0001g0118 | 2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-146+3141A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119233712 | ||||||
chr3:119233998
|
C | T | 11 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0053others(8): Show | 28 | HG00408.hp1 HG02083.hp2 HG02129.hp1 others(25): Show |
intron_variant | MODIFIER | c.-146+2855G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119233998 | ||||||
chr3:119234081
|
T | C | 31 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0001g0097others(28): Show | 52 | HG00609.hp2 HG00738.hp1 HG01123.hp1 others(49): Show |
intron_variant | MODIFIER | c.-146+2772A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119234081 | ||||||
chr3:119234116
|
G | GTT | 11 | a0001c0001t0001g0015a0001c0001t0001g0135a0001c0001t0001g0136others(8): Show | 20 | HG00140.hp2 HG00642.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.-146+2735_-146+273 others(6): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119234116 | ||||||
chr3:119234221
|
G | A | 2 | a0002c0002t0008g0026a0002c0002t0008g0134 | 4 | HG01884.hp1 HG02486.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-146+2632C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119234221 | ||||||
chr3:119234245
|
G | A | 9 | a0001c0001t0001g0023a0001c0001t0001g0138a0001c0001t0001g0139others(6): Show | 12 | HG01168.hp2 HG01346.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-146+2608C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119234245 | ||||||
chr3:119234302
|
T | C | 10 | a0001c0001t0001g0015a0001c0001t0001g0135a0001c0001t0001g0136others(7): Show | 19 | HG00140.hp2 HG00642.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.-146+2551A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119234302 | ||||||
chr3:119234328
|
C | T | 1 | a0001c0004t0001g0091 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-146+2525G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119234328 | ||||||
chr3:119234364
|
C | G | 63 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0053others(60): Show | 111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.-146+2489G>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119234364 | ||||||
chr3:119234443
|
C | A | 11 | a0001c0001t0001g0015a0001c0001t0001g0135a0001c0001t0001g0136others(8): Show | 20 | HG00140.hp2 HG00642.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.-146+2410G>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119234443 | ||||||
chr3:119234459
|
T | C | 9 | a0001c0001t0001g0023a0001c0001t0001g0138a0001c0001t0001g0139others(6): Show | 12 | HG01168.hp2 HG01346.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-146+2394A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119234459 | ||||||
chr3:119234507
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-146+2346C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119234507 | ||||||
chr3:119234545
|
T | C | 1 | a0001c0003t0002g0216 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-146+2308A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119234545 | ||||||
chr3:119234554
|
T | C | 1 | a0001c0001t0001g0068 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-146+2299A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119234554 | ||||||
chr3:119234613
|
A | G | 2 | a0001c0003t0001g0038a0001c0003t0001g0113 | 3 | HG02129.hp2 NA18994.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.-146+2240T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119234613 | ||||||
chr3:119234695
|
G | A | 1 | a0001c0001t0003g0218 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-146+2158C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119234695 | ||||||
chr3:119234722
|
G | A | 176 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(173): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.-146+2131C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119234722 | ||||||
chr3:119234844
|
C | T | 15 | a0001c0001t0001g0194a0001c0001t0001g0197a0002c0002t0004g0004others(12): Show | 32 | HG00423.hp2 HG01109.hp1 HG01952.hp2 others(29): Show |
intron_variant | MODIFIER | c.-146+2009G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119234844 | ||||||
chr3:119234864
|
C | T | 1 | a0002c0002t0001g0077 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-146+1989G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119234864 | ||||||
chr3:119234948
|
G | A | 1 | a0002c0002t0001g0117 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-146+1905C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119234948 | ||||||
chr3:119234976
|
T | C | 2 | a0001c0001t0002g0164a0001c0001t0002g0183 | 2 | HG02451.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-146+1877A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119234976 | ||||||
chr3:119235202
|
T | G | 5 | a0002c0002t0005g0031a0002c0002t0005g0064a0002c0002t0005g0075others(2): Show | 6 | HG01074.hp1 HG01081.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.-146+1651A>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119235202 | ||||||
chr3:119235347
|
T | C | 1 | a0001c0001t0002g0040 | 2 | NA18957.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.-146+1506A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119235347 | ||||||
chr3:119235388
|
C | T | 1 | a0001c0001t0002g0191 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-146+1465G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119235388 | ||||||
chr3:119235538
|
C | T | 1 | a0001c0001t0003g0170 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-146+1315G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119235538 | ||||||
chr3:119235539
|
T | C | 51 | a0001c0001t0001g0061a0001c0001t0001g0068a0001c0001t0001g0095others(48): Show | 101 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.-146+1314A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119235539 | ||||||
chr3:119235552
|
A | C | 20 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0036others(17): Show | 31 | HG00438.hp2 HG00673.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.-146+1301T>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119235552 | ||||||
chr3:119235596
|
C | A | 52 | a0001c0001t0003g0003a0001c0001t0003g0017a0001c0001t0003g0018others(49): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.-146+1257G>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119235596 | ||||||
chr3:119235664
|
C | G | 1 | a0001c0001t0003g0149 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-146+1189G>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119235664 | ||||||
chr3:119235925
|
G | A | 12 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0053others(9): Show | 29 | HG00408.hp1 HG01891.hp2 HG02083.hp2 others(26): Show |
intron_variant | MODIFIER | c.-146+928C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119235925 | ||||||
chr3:119235967
|
GA | G | 2 | a0001c0003t0002g0007a0001c0003t0002g0202 | 9 | NA18747.hp2 NA18941.hp1 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.-146+885delT | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119235967 | ||||||
chr3:119236025
|
G | A | 1 | a0002c0002t0005g0076 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-146+828C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119236025 | ||||||
chr3:119236084
|
T | C | 176 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(173): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.-146+769A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119236084 | ||||||
chr3:119236151
|
A | G | 1 | a0001c0003t0002g0050 | 2 | NA18953.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-146+702T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119236151 | ||||||
chr3:119236156
|
A | G | 11 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0053others(8): Show | 28 | HG00408.hp1 HG02083.hp2 HG02129.hp1 others(25): Show |
intron_variant | MODIFIER | c.-146+697T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119236156 | ||||||
chr3:119236223
|
A | C | 1 | a0001c0001t0001g0036 | 2 | HG01255.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.-146+630T>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119236223 | ||||||
chr3:119236224
|
C | G | 1 | a0002c0002t0011g0169 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-146+629G>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119236224 | ||||||
chr3:119236254
|
A | G | 11 | a0001c0001t0001g0015a0001c0001t0001g0135a0001c0001t0001g0136others(8): Show | 20 | HG00140.hp2 HG00642.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.-146+599T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119236254 | ||||||
chr3:119236311
|
G | GA | 190 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0023others(187): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.-146+541dupT | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119236311 | ||||||
chr3:119236406
|
A | T | 1 | a0001c0001t0001g0118 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-146+447T>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119236406 | ||||||
chr3:119236633
|
C | T | 10 | a0001c0001t0001g0015a0001c0001t0001g0135a0001c0001t0001g0136others(7): Show | 19 | HG00140.hp2 HG00642.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.-146+220G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119236633 | ||||||
chr3:119236675
|
A | G | 1 | a0001c0003t0002g0213 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-146+178T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119236675 | ||||||
chr3:119236764
|
A | G | 203 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(200): Show | 393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.-146+89T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119236764 | ||||||
chr3:119236796
|
A | C | 2 | a0001c0001t0001g0097a0001c0001t0001g0118 | 2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-146+57T>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119236796 | ||||||
chr3:119237173
|
T | C | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | HG01168.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.-363-103A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119237173 | ||||||
chr3:119237208
|
G | C | 2 | a0001c0001t0003g0159a0001c0001t0003g0160 | 2 | HG01934.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-363-138C>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119237208 | ||||||
chr3:119237272
|
C | CCTT | 101 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0014others(98): Show | 178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.-363-205_-363-203d others(5): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119237272 | ||||||
chr3:119237406
|
T | G | 1 | a0001c0001t0001g0107 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-363-336A>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119237406 | ||||||
chr3:119237448
|
G | A | 1 | a0001c0003t0002g0213 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-363-378C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119237448 | ||||||
chr3:119237559
|
T | G | 2 | a0001c0001t0001g0023a0001c0001t0001g0097 | 4 | HG02809.hp2 HG03516.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-363-489A>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119237559 | ||||||
chr3:119237594
|
A | G | 4 | a0001c0001t0001g0068a0001c0001t0001g0095a0001c0004t0001g0030others(1): Show | 5 | HG01891.hp1 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-363-524T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119237594 | ||||||
chr3:119237606
|
C | T | 1 | a0002c0002t0015g0119 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-363-536G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119237606 | ||||||
chr3:119237659
|
G | A | 8 | a0001c0001t0001g0015a0001c0001t0001g0135a0001c0001t0001g0136others(5): Show | 15 | HG00140.hp2 HG00642.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.-363-589C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119237659 | ||||||
chr3:119237932
|
A | G | 51 | a0001c0001t0001g0061a0001c0001t0001g0068a0001c0001t0001g0095others(48): Show | 101 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.-363-862T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119237932 | ||||||
chr3:119237975
|
A | G | 1 | a0001c0001t0002g0120 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-363-905T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119237975 | ||||||
chr3:119238033
|
G | A | 6 | a0001c0001t0001g0061a0002c0002t0005g0031a0002c0002t0005g0064others(3): Show | 7 | HG01074.hp1 HG01081.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.-363-963C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119238033 | ||||||
chr3:119238037
|
C | T | 3 | a0002c0002t0006g0034a0002c0002t0006g0065a0002c0002t0006g0066 | 4 | HG02257.hp2 HG02647.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-363-967G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119238037 | ||||||
chr3:119238053
|
G | A | 1 | a0002c0002t0008g0098 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-363-983C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119238053 | ||||||
chr3:119238171
|
G | A | 1 | a0002c0002t0001g0117 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-363-1101C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119238171 | ||||||
chr3:119238263
|
T | TA | 83 | a0001c0001t0001g0097a0001c0001t0001g0107a0001c0001t0002g0006others(80): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.-363-1194dupT | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119238263 | ||||||
chr3:119238263
|
T | TAA | 14 | a0001c0001t0001g0015a0001c0001t0001g0135a0001c0001t0001g0136others(11): Show | 21 | HG00140.hp2 HG00642.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.-363-1195_-363-119 others(6): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119238263 | ||||||
chr3:119238263
|
TA | T | 6 | a0001c0001t0001g0128a0001c0001t0002g0183a0001c0003t0002g0200others(3): Show | 6 | HG01081.hp1 HG01993.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-363-1194delT | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119238263 | ||||||
chr3:119238367
|
C | T | 1 | a0002c0002t0001g0117 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-363-1297G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119238367 | ||||||
chr3:119238405
|
T | C | 11 | a0001c0001t0001g0015a0001c0001t0001g0135a0001c0001t0001g0136others(8): Show | 20 | HG00140.hp2 HG00642.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.-363-1335A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119238405 | ||||||
chr3:119238522
|
C | T | 1 | a0001c0001t0002g0183 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-363-1452G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119238522 | ||||||
chr3:119238523
|
G | A | 75 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0036others(72): Show | 137 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.-363-1453C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119238523 | ||||||
chr3:119238643
|
C | T | 11 | a0001c0001t0001g0015a0001c0001t0001g0135a0001c0001t0001g0136others(8): Show | 20 | HG00140.hp2 HG00642.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.-363-1573G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119238643 | ||||||
chr3:119238697
|
C | A | 27 | a0001c0001t0002g0203a0001c0001t0002g0212a0001c0003t0002g0001others(24): Show | 78 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.-363-1627G>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119238697 | ||||||
chr3:119238701
|
G | A | 1 | a0001c0001t0002g0039 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-363-1631C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119238701 | ||||||
chr3:119238725
|
C | T | 12 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0118others(9): Show | 20 | HG01433.hp2 HG01496.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-363-1655G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119238725 | ||||||
chr3:119238780
|
C | T | 1 | a0002c0002t0001g0090 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-363-1710G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119238780 | ||||||
chr3:119238984
|
C | T | 1 | a0001c0003t0002g0186 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-364+1866G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119238984 | ||||||
chr3:119239043
|
A | G | 4 | a0001c0001t0003g0027a0001c0001t0003g0147a0001c0001t0003g0162others(1): Show | 6 | HG02280.hp1 HG02572.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-364+1807T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119239043 | ||||||
chr3:119239066
|
A | T | 176 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(173): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.-364+1784T>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119239066 | ||||||
chr3:119239089
|
T | A | 2 | a0001c0001t0002g0108a0001c0001t0002g0109 | 2 | HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-364+1761A>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119239089 | ||||||
chr3:119239248
|
C | T | 1 | a0001c0009t0002g0096 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-364+1602G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119239248 | ||||||
chr3:119239325
|
C | CA | 22 | a0001c0001t0001g0118a0001c0001t0003g0003a0001c0001t0003g0017others(19): Show | 41 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(38): Show |
intron_variant | MODIFIER | c.-364+1524dupT | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119239325 | ||||||
chr3:119239325
|
C | CAA | 41 | a0001c0001t0001g0023a0001c0001t0001g0061a0001c0001t0001g0097others(38): Show | 57 | HG00544.hp1 HG00639.hp1 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.-364+1523_-364+152 others(6): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119239325 | ||||||
chr3:119239325
|
C | CAAA | 69 | a0001c0001t0001g0014a0001c0001t0001g0068a0001c0001t0001g0095others(66): Show | 136 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.-364+1522_-364+152 others(7): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119239325 | ||||||
chr3:119239325
|
C | CAAAA | 34 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(31): Show | 63 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.-364+1521_-364+152 others(8): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119239325 | ||||||
chr3:119239325
|
C | CAAAAA | 12 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0110others(9): Show | 20 | HG01070.hp1 HG01071.hp1 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.-364+1520_-364+152 others(9): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119239325 | ||||||
chr3:119239356
|
G | A | 177 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(174): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.-364+1494C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119239356 | ||||||
chr3:119239514
|
T | G | 1 | a0001c0001t0012g0133 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-364+1336A>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119239514 | ||||||
chr3:119239696
|
T | A | 1 | a0001c0003t0002g0216 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-364+1154A>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119239696 | ||||||
chr3:119239759
|
T | C | 1 | a0001c0001t0002g0183 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-364+1091A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119239759 | ||||||
chr3:119239772
|
C | A | 62 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0053others(59): Show | 109 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.-364+1078G>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119239772 | ||||||
chr3:119239780
|
C | G | 1 | a0001c0009t0002g0096 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-364+1070G>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119239780 | ||||||
chr3:119239838
|
C | A | 11 | a0001c0001t0001g0015a0001c0001t0001g0135a0001c0001t0001g0136others(8): Show | 20 | HG00140.hp2 HG00642.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.-364+1012G>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119239838 | ||||||
chr3:119239852
|
C | T | 1 | a0001c0001t0003g0144 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-364+998G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119239852 | ||||||
chr3:119239905
|
G | T | 3 | a0001c0003t0002g0059a0002c0002t0001g0057a0002c0002t0001g0058 | 3 | NA18946.hp2 NA19006.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.-364+945C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119239905 | ||||||
chr3:119239997
|
TA | T | 87 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0023others(84): Show | 159 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.-364+852delT | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119239997 | ||||||
chr3:119239997
|
TAA | T | 88 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0014others(85): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.-364+851_-364+852d others(4): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119239997 | ||||||
chr3:119240000
|
A | T | 1 | a0001c0001t0001g0140 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-364+850T>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119240000 | ||||||
chr3:119240032
|
G | A | 7 | a0001c0001t0001g0014a0001c0001t0001g0128a0001c0001t0001g0131others(4): Show | 11 | HG01433.hp2 HG02055.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-364+818C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119240032 | ||||||
chr3:119240044
|
A | G | 11 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0053others(8): Show | 28 | HG00408.hp1 HG02083.hp2 HG02129.hp1 others(25): Show |
intron_variant | MODIFIER | c.-364+806T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119240044 | ||||||
chr3:119240045
|
T | C | 6 | a0001c0001t0001g0005a0001c0001t0001g0053a0001c0001t0001g0219others(3): Show | 17 | HG00408.hp1 NA18943.hp1 NA18944.hp2 others(14): Show |
intron_variant | MODIFIER | c.-364+805A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119240045 | ||||||
chr3:119240071
|
A | T | 23 | a0001c0001t0001g0014a0001c0001t0001g0118a0001c0001t0001g0128others(20): Show | 41 | HG00609.hp2 HG00738.hp1 HG01123.hp1 others(38): Show |
intron_variant | MODIFIER | c.-364+779T>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119240071 | ||||||
chr3:119240107
|
G | T | 11 | a0001c0001t0001g0015a0001c0001t0001g0135a0001c0001t0001g0136others(8): Show | 20 | HG00140.hp2 HG00642.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.-364+743C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119240107 | ||||||
chr3:119240193
|
A | G | 21 | a0001c0001t0001g0014a0001c0001t0001g0118a0001c0001t0001g0128others(18): Show | 39 | HG00609.hp2 HG00738.hp1 HG01123.hp1 others(36): Show |
intron_variant | MODIFIER | c.-364+657T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119240193 | ||||||
chr3:119240202
|
T | C | 1 | a0002c0002t0006g0034 | 2 | HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-364+648A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119240202 | ||||||
chr3:119240222
|
A | T | 1 | a0002c0002t0001g0117 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-364+628T>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119240222 | ||||||
chr3:119240241
|
G | GT | 5 | a0001c0001t0002g0025a0001c0001t0002g0039a0001c0001t0002g0114others(2): Show | 8 | HG00140.hp2 HG00642.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.-364+608dupA | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119240241 | ||||||
chr3:119240363
|
C | T | 78 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0024others(75): Show | 142 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.-364+487G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119240363 | ||||||
chr3:119240468
|
A | C | 52 | a0001c0001t0001g0061a0001c0001t0001g0068a0001c0001t0001g0095others(49): Show | 102 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.-364+382T>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119240468 | ||||||
chr3:119240757
|
G | A | 1 | a0003c0006t0002g0054 | 2 | HG03491.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-364+93C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119240757 | ||||||
chr3:119240823
|
G | T | 1 | a0001c0005t0010g0055 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-364+27C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119240823 |