geneid | 27087 |
---|---|
ensemblid | ENSG00000109956.13 |
hgncid | 921 |
symbol | B3GAT1 |
name | beta-1,3-glucuronyltransferase 1 |
refseq_nuc | NM_054025.3 |
refseq_prot | NP_473366.1 |
ensembl_nuc | ENST00000312527.9 |
ensembl_prot | ENSP00000307875.4 |
mane_status | MANE Select |
chr | chr11 |
start | 134378508 |
end | 134412242 |
strand | - |
ver | v1.2 |
region | chr11:134378508-134412242 |
region5000 | chr11:134373508-134417242 |
regionname0 | B3GAT1_chr11_134378508_134412242 |
regionname5000 | B3GAT1_chr11_134373508_134417242 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 334 | 334 | 79 | 74 | 121 | 18 | 40 | 81 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0002 | 0/0 | 334 | 17 | 15 | 2 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0003 | 0/0 | 334 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1005 | 328 | 73 | 74 | 121 | 18 | 40 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
c0002 | 0/0 | 1005 | 17 | 15 | 2 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
c0003 | 0/0 | 1005 | 6 | 6 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
c0004 | 0/0 | 1005 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 2992 | 135 | 19 | 24 | 68 | 8 | 16 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0002 | 0/0 | 2972 | 35 | 13 | 14 | 6 | 2 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0003 | 0/1 | 2992 | 30 | 13 | 7 | 3 | 0 | 6 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0004 | 0/0 | 3007 | 21 | 14 | 2 | 5 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0005 | 1/0 | 2972 | 18 | 7 | 3 | 3 | 2 | 2 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0006 | 0/0 | 2993 | 15 | 1 | 3 | 7 | 1 | 3 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0007 | 0/0 | 2992 | 11 | 0 | 5 | 4 | 0 | 2 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0008 | 0/0 | 3011 | 8 | 1 | 3 | 0 | 2 | 2 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0009 | 0/0 | 2988 | 6 | 0 | 0 | 5 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0010 | 0/0 | 2992 | 5 | 3 | 2 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0011 | 0/0 | 2993 | 4 | 2 | 2 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0012 | 0/0 | 3007 | 4 | 4 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0013 | 0/0 | 2991 | 4 | 3 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0014 | 0/0 | 3008 | 3 | 1 | 0 | 2 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0015 | 0/0 | 2973 | 3 | 1 | 1 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0016 | 0/0 | 2994 | 2 | 1 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0017 | 0/0 | 2993 | 2 | 0 | 0 | 2 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0018 | 0/0 | 3008 | 2 | 0 | 2 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0019 | 0/0 | 2993 | 2 | 1 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0020 | 0/0 | 2992 | 2 | 0 | 0 | 2 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0021 | 0/0 | 2992 | 2 | 2 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0022 | 0/0 | 3007 | 2 | 0 | 1 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0023 | 0/0 | 2972 | 2 | 0 | 0 | 2 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0024 | 0/0 | 2972 | 2 | 0 | 1 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0025 | 0/0 | 2994 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0026 | 0/0 | 2991 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0027 | 0/0 | 2993 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0028 | 0/0 | 2993 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0029 | 0/0 | 2993 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0030 | 0/0 | 2973 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0031 | 0/0 | 2973 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0032 | 0/0 | 2992 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0033 | 0/0 | 2989 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0034 | 0/0 | 2994 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0035 | 0/0 | 2992 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0036 | 0/0 | 3012 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0037 | 0/0 | 2993 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0038 | 0/0 | 2989 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0039 | 0/0 | 2992 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0040 | 0/0 | 2992 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0041 | 0/0 | 2992 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0042 | 0/0 | 2992 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0043 | 0/0 | 3011 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0044 | 0/0 | 3011 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0045 | 0/0 | 2992 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0046 | 0/0 | 2988 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0047 | 0/0 | 3007 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0048 | 0/0 | 3007 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0049 | 0/0 | 2972 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0050 | 0/0 | 2973 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0051 | 0/0 | 2973 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0052 | 0/0 | 2991 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0053 | 0/0 | 2972 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0054 | 0/0 | 2972 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0055 | 0/0 | 2972 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
t0056 | 0/0 | 2992 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0066 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0331 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1005 | 328 | 73 | 74 | 121 | 18 | 40 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0003 | 0/0 | 1005 | 6 | 6 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0002c0002 | 0/0 | 1005 | 17 | 15 | 2 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0003c0004 | 0/0 | 1005 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3996 | 123 | 9 | 23 | 67 | 8 | 16 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0002 | 0/0 | 3976 | 31 | 9 | 14 | 6 | 2 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0003 | 0/1 | 3996 | 30 | 13 | 7 | 3 | 0 | 6 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0004 | 0/0 | 4011 | 17 | 10 | 2 | 5 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0005 | 1/0 | 3976 | 18 | 7 | 3 | 3 | 2 | 2 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0006 | 0/0 | 3997 | 13 | 0 | 2 | 7 | 1 | 3 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0007 | 0/0 | 3996 | 11 | 0 | 5 | 4 | 0 | 2 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0008 | 0/0 | 4015 | 8 | 1 | 3 | 0 | 2 | 2 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0009 | 0/0 | 3992 | 6 | 0 | 0 | 5 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0010 | 0/0 | 3996 | 5 | 3 | 2 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0011 | 0/0 | 3997 | 4 | 2 | 2 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0012 | 0/0 | 4011 | 4 | 4 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0013 | 0/0 | 3995 | 4 | 3 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0014 | 0/0 | 4012 | 3 | 1 | 0 | 2 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0015 | 0/0 | 3977 | 3 | 1 | 1 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0016 | 0/0 | 3998 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0017 | 0/0 | 3997 | 2 | 0 | 0 | 2 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0018 | 0/0 | 4012 | 2 | 0 | 2 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0019 | 0/0 | 3997 | 2 | 1 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0020 | 0/0 | 3996 | 2 | 0 | 0 | 2 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0021 | 0/0 | 3996 | 2 | 2 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0022 | 0/0 | 4011 | 2 | 0 | 1 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0023 | 0/0 | 3976 | 2 | 0 | 0 | 2 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0024 | 0/0 | 3976 | 2 | 0 | 1 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0025 | 0/0 | 3998 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0026 | 0/0 | 3995 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0027 | 0/0 | 3997 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0028 | 0/0 | 3997 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0029 | 0/0 | 3997 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0030 | 0/0 | 3977 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0031 | 0/0 | 3977 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0032 | 0/0 | 3996 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0033 | 0/0 | 3993 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0034 | 0/0 | 3998 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0035 | 0/0 | 3996 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0036 | 0/0 | 4016 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0037 | 0/0 | 3997 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0038 | 0/0 | 3993 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0039 | 0/0 | 3996 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0040 | 0/0 | 3996 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0041 | 0/0 | 3996 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0042 | 0/0 | 3996 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0043 | 0/0 | 4015 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0044 | 0/0 | 4015 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0045 | 0/0 | 3996 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0046 | 0/0 | 3992 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0047 | 0/0 | 4011 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0049 | 0/0 | 3976 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0050 | 0/0 | 3977 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0051 | 0/0 | 3977 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0052 | 0/0 | 3995 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0053 | 0/0 | 3976 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0054 | 0/0 | 3976 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0055 | 0/0 | 3976 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0001t0056 | 0/0 | 3996 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0003t0001 | 0/0 | 3996 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0003t0004 | 0/0 | 4011 | 4 | 4 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0001c0003t0048 | 0/0 | 4011 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0002c0002t0001 | 0/0 | 3996 | 10 | 9 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0002c0002t0002 | 0/0 | 3976 | 4 | 4 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0002c0002t0006 | 0/0 | 3997 | 2 | 1 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0002c0002t0016 | 0/0 | 3998 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
a0003c0004t0001 | 0/0 | 3996 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | copy fasta | chr11 | 134373508 | 134417242 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0002g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0002g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0003g0066 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0004g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0004g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0005g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0005g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0005g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0005g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0005g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0005g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0005g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0005g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0005g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0005g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0005g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0005g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0005g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0005g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0005g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0005g0331 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0005g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0005g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0006g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0006g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0006g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0006g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0006g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0006g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0006g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0006g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0006g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0006g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0006g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0006g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0007g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0007g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0007g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0007g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0007g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0007g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0007g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0007g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0007g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0008g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0008g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0008g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0008g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0008g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0008g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0008g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0009g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0009g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0009g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0009g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0009g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0009g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0010g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0010g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0010g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0010g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0011g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0011g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0011g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0011g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0012g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0012g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0012g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0012g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0013g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0013g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0013g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0013g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0014g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0014g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0014g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0015g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0015g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0015g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0016g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0017g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0017g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0018g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0018g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0019g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0019g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0020g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0020g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0021g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0021g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0022g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0022g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0023g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0023g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0024g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0024g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0025g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0026g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0027g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0028g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0029g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0030g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0031g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0032g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0033g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0034g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0035g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0036g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0037g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0038g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0039g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0040g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0041g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0042g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0043g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0044g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0045g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0046g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0047g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0049g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0050g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0051g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0052g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0053g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0054g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0055g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0001t0056g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0003t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0003t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0003t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0003t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0003t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0001c0003t0048g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0002c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0002c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0002c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0002c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0002c0002t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0002c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0002c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0002c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0002c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0002c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0002c0002t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0002c0002t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0002c0002t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0002c0002t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0002c0002t0006g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0002c0002t0006g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0002c0002t0016g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
a0003c0004t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | GBR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG00099 | hp2 | a0001 | c0001 | t0049 | g0271 | EUR | GBR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0123 | EUR | GBR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG00140 | hp2 | a0001 | c0001 | t0008 | g0008 | EUR | GBR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG00280 | hp1 | a0001 | c0001 | t0052 | g0291 | EUR | FIN | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0079 | EUR | FIN | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG00323 | hp1 | a0001 | c0001 | t0008 | g0117 | EUR | FIN | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0294 | EUR | FIN | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG00408 | hp1 | a0001 | c0001 | t0028 | g0019 | EAS | CHS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG00438 | hp1 | a0001 | c0001 | t0005 | g0316 | EAS | CHS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG00438 | hp2 | a0001 | c0001 | t0020 | g0139 | EAS | CHS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG00544 | hp1 | a0001 | c0001 | t0007 | g0199 | EAS | CHS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG00544 | hp2 | a0001 | c0001 | t0027 | g0016 | EAS | CHS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | CHS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | CHS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0085 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG00642 | hp2 | a0001 | c0001 | t0015 | g0273 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG00673 | hp2 | a0001 | c0001 | t0007 | g0089 | EAS | CHS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG00735 | hp1 | a0001 | c0001 | t0008 | g0105 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG00735 | hp2 | a0001 | c0001 | t0006 | g0043 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG00738 | hp2 | a0001 | c0001 | t0006 | g0047 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01069 | hp1 | a0001 | c0001 | t0007 | g0003 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01070 | hp1 | a0001 | c0001 | t0005 | g0295 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01070 | hp2 | a0001 | c0001 | t0007 | g0009 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01071 | hp1 | a0001 | c0001 | t0007 | g0003 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01071 | hp2 | a0001 | c0001 | t0007 | g0185 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01074 | hp1 | a0001 | c0001 | t0005 | g0308 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01074 | hp2 | a0002 | c0002 | t0006 | g0050 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0324 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01106 | hp1 | a0001 | c0001 | t0024 | g0304 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01109 | hp2 | a0001 | c0001 | t0050 | g0272 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0136 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01168 | hp2 | a0001 | c0001 | t0054 | g0285 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01169 | hp1 | a0001 | c0001 | t0031 | g0026 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01169 | hp2 | a0001 | c0001 | t0029 | g0020 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01175 | hp1 | a0001 | c0001 | t0007 | g0009 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01192 | hp1 | a0001 | c0001 | t0011 | g0035 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0083 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01243 | hp1 | a0002 | c0002 | t0001 | g0227 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0322 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0059 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01256 | hp1 | a0001 | c0001 | t0022 | g0257 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01257 | hp1 | a0001 | c0001 | t0004 | g0011 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0300 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01258 | hp2 | a0001 | c0001 | t0004 | g0011 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01261 | hp1 | a0001 | c0001 | t0016 | g0017 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01261 | hp2 | a0001 | c0001 | t0018 | g0024 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0313 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0315 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01358 | hp1 | a0001 | c0001 | t0010 | g0004 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01358 | hp2 | a0001 | c0001 | t0005 | g0329 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01433 | hp1 | a0001 | c0001 | t0008 | g0197 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01496 | hp2 | a0001 | c0001 | t0013 | g0317 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0215 | EUR | IBS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01515 | hp2 | a0001 | c0001 | t0005 | g0289 | EUR | IBS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0172 | EUR | IBS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0216 | EUR | IBS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0192 | AFR | ACB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0330 | AFR | ACB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0326 | AFR | ACB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01891 | hp2 | a0002 | c0002 | t0001 | g0229 | AFR | ACB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0126 | AMR | PEL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01934 | hp1 | a0001 | c0001 | t0018 | g0023 | AMR | PEL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0115 | AMR | PEL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PEL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01952 | hp1 | a0001 | c0001 | t0010 | g0004 | AMR | PEL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0286 | AMR | PEL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0299 | AMR | PEL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0309 | AMR | PEL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01981 | hp2 | a0001 | c0001 | t0011 | g0036 | AMR | PEL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02015 | hp2 | a0001 | c0001 | t0009 | g0244 | EAS | KHV | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02040 | hp1 | a0001 | c0001 | t0023 | g0280 | EAS | KHV | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02055 | hp1 | a0002 | c0002 | t0001 | g0228 | AFR | ACB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02055 | hp2 | a0001 | c0001 | t0003 | g0191 | AFR | ACB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | KHV | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02056 | hp2 | a0001 | c0001 | t0046 | g0245 | EAS | KHV | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02080 | hp1 | a0001 | c0001 | t0056 | g0338 | EAS | KHV | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02080 | hp2 | a0001 | c0001 | t0007 | g0098 | EAS | KHV | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02083 | hp2 | a0001 | c0001 | t0007 | g0121 | EAS | KHV | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02129 | hp2 | a0001 | c0001 | t0032 | g0027 | EAS | KHV | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02132 | hp2 | a0001 | c0001 | t0006 | g0002 | EAS | KHV | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02135 | hp1 | a0001 | c0001 | t0006 | g0002 | EAS | KHV | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02145 | hp1 | a0001 | c0001 | t0015 | g0275 | AFR | ACB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0070 | AFR | ACB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0060 | AFR | ACB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02257 | hp2 | a0001 | c0001 | t0039 | g0221 | AFR | ACB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02258 | hp1 | a0002 | c0002 | t0016 | g0018 | AFR | ACB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02258 | hp2 | a0001 | c0003 | t0001 | g0235 | AFR | ACB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PEL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02280 | hp1 | a0002 | c0002 | t0002 | g0334 | AFR | ACB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0333 | AFR | ACB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02293 | hp2 | a0001 | c0001 | t0008 | g0008 | AMR | PEL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0306 | AMR | PEL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0165 | AFR | ACB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02451 | hp2 | a0001 | c0001 | t0004 | g0252 | AFR | ACB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02572 | hp1 | a0001 | c0003 | t0004 | g0249 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02572 | hp2 | a0001 | c0001 | t0013 | g0318 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0104 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02602 | hp2 | a0001 | c0001 | t0008 | g0161 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0195 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02622 | hp1 | a0002 | c0002 | t0001 | g0194 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02622 | hp2 | a0001 | c0001 | t0021 | g0056 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02630 | hp1 | a0002 | c0002 | t0001 | g0234 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02630 | hp2 | a0001 | c0001 | t0053 | g0321 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02647 | hp1 | a0002 | c0002 | t0006 | g0051 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02647 | hp2 | a0001 | c0001 | t0011 | g0038 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02683 | hp2 | a0001 | c0001 | t0005 | g0319 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0176 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02717 | hp1 | a0001 | c0003 | t0048 | g0268 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02717 | hp2 | a0001 | c0001 | t0004 | g0248 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02723 | hp1 | a0002 | c0002 | t0001 | g0082 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02723 | hp2 | a0001 | c0001 | t0012 | g0270 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0177 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02738 | hp1 | a0001 | c0001 | t0006 | g0039 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02738 | hp2 | a0001 | c0001 | t0022 | g0258 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02809 | hp1 | a0001 | c0001 | t0010 | g0061 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02809 | hp2 | a0001 | c0001 | t0010 | g0189 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02818 | hp1 | a0001 | c0001 | t0013 | g0332 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02818 | hp2 | a0002 | c0002 | t0001 | g0190 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0226 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02886 | hp2 | a0001 | c0001 | t0005 | g0290 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02896 | hp1 | a0001 | c0001 | t0004 | g0269 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02896 | hp2 | a0001 | c0001 | t0014 | g0054 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02897 | hp1 | a0001 | c0001 | t0044 | g0057 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0260 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0001 | AFR | ESN | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | ESN | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0292 | AFR | ESN | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02965 | hp2 | a0002 | c0002 | t0001 | g0225 | AFR | ESN | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0323 | AFR | ESN | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ESN | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02976 | hp1 | a0001 | c0001 | t0012 | g0263 | AFR | ESN | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02976 | hp2 | a0002 | c0002 | t0002 | g0293 | AFR | ESN | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03017 | hp1 | a0001 | c0001 | t0006 | g0034 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0277 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03041 | hp2 | a0001 | c0001 | t0004 | g0264 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03098 | hp1 | a0001 | c0001 | t0005 | g0301 | AFR | MSL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | MSL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03130 | hp1 | a0001 | c0001 | t0004 | g0001 | AFR | ESN | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03130 | hp2 | a0001 | c0001 | t0005 | g0328 | AFR | ESN | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | ESN | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0262 | AFR | ESN | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03195 | hp2 | a0001 | c0001 | t0019 | g0049 | AFR | ESN | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0314 | AFR | MSL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03209 | hp2 | a0001 | c0001 | t0013 | g0297 | AFR | MSL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03225 | hp1 | a0001 | c0001 | t0005 | g0335 | AFR | MSL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03225 | hp2 | a0001 | c0001 | t0005 | g0336 | AFR | MSL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03239 | hp1 | a0001 | c0001 | t0007 | g0231 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03239 | hp2 | a0001 | c0001 | t0015 | g0276 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0094 | AFR | MSL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0312 | AFR | MSL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03486 | hp1 | a0002 | c0002 | t0001 | g0219 | AFR | MSL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03486 | hp2 | a0001 | c0003 | t0004 | g0267 | AFR | MSL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03492 | hp1 | a0001 | c0001 | t0024 | g0288 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03516 | hp1 | a0001 | c0001 | t0011 | g0031 | AFR | ESN | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03516 | hp2 | a0001 | c0001 | t0004 | g0261 | AFR | ESN | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03540 | hp1 | a0001 | c0003 | t0004 | g0250 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03540 | hp2 | a0001 | c0001 | t0010 | g0232 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03579 | hp1 | a0002 | c0002 | t0002 | g0305 | AFR | MSL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0058 | AFR | MSL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03654 | hp1 | a0001 | c0001 | t0005 | g0320 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03688 | hp1 | a0001 | c0001 | t0006 | g0040 | SAS | STU | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03688 | hp2 | a0001 | c0001 | t0033 | g0028 | SAS | STU | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0222 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0186 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03710 | hp2 | a0001 | c0001 | t0019 | g0033 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | BEB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03831 | hp2 | a0001 | c0001 | t0036 | g0045 | SAS | BEB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | BEB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | BEB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03927 | hp1 | a0001 | c0001 | t0025 | g0014 | SAS | BEB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | BEB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03942 | hp1 | a0001 | c0001 | t0007 | g0220 | SAS | BEB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0179 | SAS | BEB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | STU | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | STU | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | STU | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG04199 | hp2 | a0001 | c0001 | t0035 | g0030 | SAS | STU | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG04204 | hp1 | a0001 | c0001 | t0008 | g0209 | SAS | STU | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | STU | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18522 | hp1 | a0001 | c0001 | t0012 | g0266 | AFR | YRI | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18522 | hp2 | a0001 | c0003 | t0004 | g0251 | AFR | YRI | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | CHB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0203 | EAS | CHB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CHB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18747 | hp2 | a0001 | c0001 | t0005 | g0278 | EAS | CHB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18939 | hp1 | a0001 | c0001 | t0004 | g0254 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18940 | hp1 | a0001 | c0001 | t0006 | g0037 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18940 | hp2 | a0001 | c0001 | t0051 | g0274 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18942 | hp1 | a0001 | c0001 | t0006 | g0041 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18942 | hp2 | a0001 | c0001 | t0041 | g0096 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18948 | hp2 | a0001 | c0001 | t0009 | g0246 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18949 | hp2 | a0003 | c0004 | t0001 | g0164 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18950 | hp2 | a0001 | c0001 | t0006 | g0042 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18951 | hp2 | a0001 | c0001 | t0040 | g0150 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18954 | hp1 | a0001 | c0001 | t0009 | g0241 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18962 | hp2 | a0001 | c0001 | t0004 | g0256 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18964 | hp2 | a0001 | c0001 | t0026 | g0015 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18969 | hp1 | a0001 | c0001 | t0005 | g0279 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18982 | hp1 | a0001 | c0001 | t0023 | g0311 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18984 | hp1 | a0001 | c0001 | t0006 | g0032 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19000 | hp1 | a0001 | c0001 | t0030 | g0025 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19000 | hp2 | a0001 | c0001 | t0014 | g0053 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19010 | hp1 | a0001 | c0001 | t0009 | g0243 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19010 | hp2 | a0001 | c0001 | t0006 | g0046 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19011 | hp1 | a0001 | c0001 | t0017 | g0021 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19011 | hp2 | a0001 | c0001 | t0004 | g0255 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0149 | AFR | LWK | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0134 | AFR | LWK | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0084 | AFR | LWK | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19043 | hp2 | a0001 | c0001 | t0047 | g0247 | AFR | LWK | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19054 | hp2 | a0001 | c0001 | t0017 | g0022 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19055 | hp2 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19063 | hp2 | a0001 | c0001 | t0004 | g0253 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19065 | hp1 | a0001 | c0001 | t0004 | g0259 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19074 | hp1 | a0001 | c0001 | t0020 | g0069 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19079 | hp1 | a0001 | c0001 | t0014 | g0055 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19081 | hp1 | a0001 | c0001 | t0034 | g0029 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19084 | hp2 | a0001 | c0001 | t0038 | g0052 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19087 | hp2 | a0001 | c0001 | t0037 | g0048 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19091 | hp2 | a0001 | c0001 | t0009 | g0240 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19240 | hp1 | a0001 | c0001 | t0055 | g0287 | AFR | YRI | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0233 | AFR | YRI | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA20129 | hp1 | a0001 | c0001 | t0005 | g0327 | AFR | ASW | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ASW | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA20752 | hp1 | a0001 | c0001 | t0006 | g0044 | EUR | TSI | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA20752 | hp2 | a0001 | c0001 | t0042 | g0181 | EUR | TSI | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA20805 | hp1 | a0001 | c0001 | t0005 | g0302 | EUR | TSI | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0337 | EUR | TSI | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | GIH | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA20905 | hp2 | a0001 | c0001 | t0009 | g0242 | SAS | GIH | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0298 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG01123 | hp2 | a0001 | c0001 | t0003 | g0113 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02109 | hp1 | a0001 | c0001 | t0004 | g0001 | AFR | ACB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02109 | hp2 | a0001 | c0001 | t0008 | g0196 | AFR | ACB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02559 | hp1 | a0002 | c0002 | t0002 | g0296 | AFR | ACB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG02559 | hp2 | a0001 | c0001 | t0045 | g0223 | AFR | ACB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0081 | AFR | MSL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0325 | AFR | MSL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG06807 | hp1 | a0001 | c0001 | t0012 | g0265 | AFR | USA | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
HG06807 | hp2 | a0001 | c0001 | t0043 | g0100 | AFR | USA | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | USA | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA20300 | hp2 | a0001 | c0001 | t0005 | g0310 | AFR | USA | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA21309 | hp1 | a0001 | c0001 | t0021 | g0095 | AFR | LWK | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | LWK | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0066 | REF | REF | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0005 | g0331 | REF | REF | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:134383910
|
C | T | 1 | a0002 | 17 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(14): Show |
missense_variant | MODERATE | c.391G>A | p.Ala131Thr | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 3/6 | 1108/3976 | 391/1005 | 131/334 | chr11 | 134383910 | ||
chr11:134384040
|
G | T | 1 | a0003 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.261C>A | p.His87Gln | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 3/6 | 978/3976 | 261/1005 | 87/334 | chr11 | 134384040 | ||
chr11:134384041
|
T | G | 1 | a0003 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.260A>C | p.His87Pro | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 3/6 | 977/3976 | 260/1005 | 87/334 | chr11 | 134384041 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:134382947
|
G | A | 1 | a0001c0003 | 6 | HG02258.hp2 HG02572.hp1 HG02717.hp1 others(3): Show |
synonymous_variant | LOW | c.681C>T | p.Tyr227Tyr | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/6 | 1398/3976 | 681/1005 | 227/334 | chr11 | 134382947 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:134378669
|
C | T | 1 | a0001c0001t0044 | 1 | HG02897.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2093G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 6/6 | 3269 | chr11 | 134378669 | |||||
chr11:134379100
|
C | T | 1 | a0001c0001t0022 | 2 | HG01256.hp1 HG02738.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1662G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 6/6 | 2838 | chr11 | 134379100 | |||||
chr11:134379161
|
A | T | 2 | a0001c0001t0045a0001c0001t0053 | 2 | HG02559.hp2 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1601T>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 6/6 | 2777 | chr11 | 134379161 | |||||
chr11:134379404
|
G | A | 1 | a0001c0001t0045 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1358C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 6/6 | 2534 | chr11 | 134379404 | |||||
chr11:134379427
|
T | C | 53 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(50): Show | 287 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(284): Show |
3_prime_UTR_variant | MODIFIER | c.*1335A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 6/6 | 2511 | chr11 | 134379427 | |||||
chr11:134379428
|
G | A | 10 | a0001c0001t0010a0001c0001t0013a0001c0001t0019others(7): Show | 19 | HG01168.hp2 HG01169.hp1 HG01358.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1334C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 6/6 | 2510 | chr11 | 134379428 | |||||
chr11:134379455
|
T | C | 51 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(48): Show | 285 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(282): Show |
3_prime_UTR_variant | MODIFIER | c.*1307A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 6/6 | 2483 | chr11 | 134379455 | |||||
chr11:134379510
|
G | A | 1 | a0001c0001t0024 | 2 | HG01106.hp1 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1252C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 6/6 | 2428 | chr11 | 134379510 | |||||
chr11:134379656
|
C | T | 5 | a0001c0001t0007a0001c0001t0023a0001c0001t0024others(2): Show | 17 | HG00408.hp1 HG00544.hp1 HG00673.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1106G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 6/6 | 2282 | chr11 | 134379656 | |||||
chr11:134379712
|
G | A | 4 | a0001c0001t0008a0001c0001t0036a0001c0001t0043others(1): Show | 11 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1050C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 6/6 | 2226 | chr11 | 134379712 | |||||
chr11:134379781
|
A | ACCTTGCC others(12): Show |
6 | a0001c0001t0008a0001c0001t0013a0001c0001t0036others(3): Show | 16 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*962_*980dupCGGTGG others(13): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 6/6 | 2156 | chr11 | 134379781 | |||||
chr11:134379933
|
G | A | 2 | a0001c0001t0021a0001c0001t0055 | 3 | HG02622.hp2 NA19240.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*829C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 6/6 | 2005 | chr11 | 134379933 | |||||
chr11:134379954
|
C | T | 1 | a0001c0001t0047 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*808G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 6/6 | 1984 | chr11 | 134379954 | |||||
chr11:134380056
|
G | C | 1 | a0001c0001t0027 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*706C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 6/6 | 1882 | chr11 | 134380056 | |||||
chr11:134380113
|
C | T | 1 | a0001c0001t0043 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*649G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 6/6 | 1825 | chr11 | 134380113 | |||||
chr11:134380172
|
C | T | 1 | a0001c0001t0042 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*590G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 6/6 | 1766 | chr11 | 134380172 | |||||
chr11:134380255
|
C | T | 1 | a0001c0001t0041 | 1 | NA18942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*507G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 6/6 | 1683 | chr11 | 134380255 | |||||
chr11:134380377
|
T | G | 1 | a0001c0003t0048 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*385A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 6/6 | 1561 | chr11 | 134380377 | |||||
chr11:134380455
|
A | G | 1 | a0001c0001t0040 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*307T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 6/6 | 1483 | chr11 | 134380455 | |||||
chr11:134387723
|
C | T | 2 | a0001c0001t0020a0001c0001t0039 | 3 | HG00438.hp2 HG02257.hp2 NA19074.hp1 |
5_prime_UTR_variant | MODIFIER | c.-64G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/6 | 64 | chr11 | 134387723 | |||||
chr11:134411915
|
C | T | 1 | a0001c0001t0049 | 1 | HG00099.hp2 | 5_prime_UTR_variant | MODIFIER | c.-390G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/6 | 24256 | chr11 | 134411915 | |||||
chr11:134411916
|
T | C | 1 | a0001c0001t0049 | 1 | HG00099.hp2 | 5_prime_UTR_variant | MODIFIER | c.-391A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/6 | 24257 | chr11 | 134411916 | |||||
chr11:134411920
|
C | G | 1 | a0001c0001t0049 | 1 | HG00099.hp2 | 5_prime_UTR_variant | MODIFIER | c.-395G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/6 | 24261 | chr11 | 134411920 | |||||
chr11:134411971
|
CCGCG | C | 5 | a0001c0001t0009a0001c0001t0026a0001c0001t0033others(2): Show | 10 | HG02015.hp2 HG02056.hp2 HG03688.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-450_-447delCGCG | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/6 | 24313 | chr11 | 134411971 | |||||
chr11:134411984
|
C | CGCCCGCC others(8): Show |
8 | a0001c0001t0004a0001c0001t0012a0001c0001t0014others(5): Show | 34 | HG01256.hp1 HG01257.hp1 HG01258.hp2 others(31): Show |
5_prime_UTR_variant | MODIFIER | c.-460_-459insTGCGGG others(9): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/6 | 24326 | chr11 | 134411984 | |||||
chr11:134412093
|
C | CG | 5 | a0001c0001t0015a0001c0001t0026a0001c0001t0034others(2): Show | 7 | HG00642.hp2 HG01109.hp2 HG02145.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-569dupC | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/6 | 24435 | chr11 | 134412093 | |||||
chr11:134412093
|
C | G | 2 | a0001c0001t0027a0001c0001t0035 | 2 | HG00544.hp2 HG04199.hp2 |
5_prime_UTR_variant | MODIFIER | c.-568G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/6 | 24434 | chr11 | 134412093 | |||||
chr11:134412098
|
G | GGGCGGGG others(7): Show |
10 | a0001c0001t0006a0001c0001t0011a0001c0001t0014others(7): Show | 29 | HG00735.hp2 HG00738.hp2 HG01074.hp2 others(26): Show |
5_prime_UTR_variant | MODIFIER | c.-574_-573insTCCCCC others(8): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/6 | 24440 | chr11 | 134412098 | |||||
chr11:134412100
|
C | A | 1 | a0001c0001t0049 | 1 | HG00099.hp2 | 5_prime_UTR_variant | MODIFIER | c.-575G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/6 | 24441 | chr11 | 134412100 | |||||
chr11:134412105
|
A | G | 1 | a0001c0001t0049 | 1 | HG00099.hp2 | 5_prime_UTR_variant | MODIFIER | c.-580T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/6 | 24446 | chr11 | 134412105 | |||||
chr11:134412106
|
G | GGGGGAGC others(13): Show |
1 | a0001c0001t0056 | 1 | HG02080.hp1 | 5_prime_UTR_variant | MODIFIER | c.-601_-582dupGCTCCC others(14): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/6 | 24448 | chr11 | 134412106 | |||||
chr11:134412108
|
G | GGGAGCGG others(13): Show |
31 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(28): Show | 244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
5_prime_UTR_variant | MODIFIER | c.-584_-583insACCTCC others(14): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/6 | 24450 | chr11 | 134412108 | |||||
chr11:134412108
|
G | GGGAGCGG others(14): Show |
2 | a0001c0001t0025a0001c0001t0033 | 2 | HG03688.hp2 HG03927.hp1 |
5_prime_UTR_variant | MODIFIER | c.-584_-583insACCTCC others(15): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/6 | 24450 | chr11 | 134412108 | |||||
chr11:134412108
|
G | GGGAGCGG others(13): Show |
1 | a0001c0001t0032 | 1 | HG02129.hp2 | 5_prime_UTR_variant | MODIFIER | c.-584_-583insACCTCC others(14): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/6 | 24450 | chr11 | 134412108 | |||||
chr11:134412108
|
G | GGGGAGCG others(14): Show |
2 | a0001c0001t0026a0001c0001t0034 | 2 | NA18964.hp2 NA19081.hp1 |
5_prime_UTR_variant | MODIFIER | c.-584_-583insACCTCC others(15): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/6 | 24450 | chr11 | 134412108 | |||||
chr11:134412108
|
G | GGGGAGGT | 10 | a0001c0001t0006a0001c0001t0011a0001c0001t0014others(7): Show | 29 | HG00735.hp2 HG00738.hp2 HG01074.hp2 others(26): Show |
5_prime_UTR_variant | MODIFIER | c.-584_-583insACCTCC others(1): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/6 | 24450 | chr11 | 134412108 | |||||
chr11:134412156
|
A | AG | 11 | a0001c0001t0016a0001c0001t0017a0001c0001t0018others(8): Show | 13 | HG00408.hp1 HG00544.hp2 HG01169.hp1 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-632dupC | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/6 | 24498 | chr11 | 134412156 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:134380857
|
T | G | 1 | a0001c0001t0021g0095 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.*15-110A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 5/5 | chr11 | 134380857 | ||||||
chr11:134380880
|
G | C | 16 | a0001c0001t0047g0247a0002c0002t0001g0082a0002c0002t0001g0190others(13): Show | 16 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.*15-133C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 5/5 | chr11 | 134380880 | ||||||
chr11:134380924
|
G | T | 226 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(223): Show | 236 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.*15-177C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 5/5 | chr11 | 134380924 | ||||||
chr11:134380946
|
C | T | 28 | a0001c0001t0008g0008a0001c0001t0008g0105a0001c0001t0008g0117others(25): Show | 30 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.*15-199G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 5/5 | chr11 | 134380946 | ||||||
chr11:134380964
|
C | G | 1 | a0001c0001t0003g0202 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.*15-217G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 5/5 | chr11 | 134380964 | ||||||
chr11:134381358
|
C | T | 226 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(223): Show | 236 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.*14+566G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 5/5 | chr11 | 134381358 | ||||||
chr11:134381450
|
G | A | 1 | a0001c0001t0001g0167 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.*14+474C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 5/5 | chr11 | 134381450 | ||||||
chr11:134381599
|
C | T | 28 | a0001c0001t0008g0008a0001c0001t0008g0105a0001c0001t0008g0117others(25): Show | 30 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.*14+325G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 5/5 | chr11 | 134381599 | ||||||
chr11:134381700
|
A | G | 10 | a0001c0001t0008g0008a0001c0001t0008g0105a0001c0001t0008g0117others(7): Show | 11 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(8): Show |
intron_variant | MODIFIER | c.*14+224T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 5/5 | chr11 | 134381700 | ||||||
chr11:134381850
|
G | T | 1 | a0001c0001t0001g0062 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.*14+74C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 5/5 | chr11 | 134381850 | ||||||
chr11:134381883
|
C | A | 143 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(140): Show | 151 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.*14+41G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 5/5 | chr11 | 134381883 | ||||||
chr11:134382123
|
C | G | 1 | a0001c0001t0001g0163 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.919-99G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/5 | chr11 | 134382123 | ||||||
chr11:134382124
|
C | A | 1 | a0001c0001t0001g0163 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.919-100G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/5 | chr11 | 134382124 | ||||||
chr11:134382137
|
G | A | 2 | a0001c0001t0045g0223a0001c0001t0053g0321 | 2 | HG02559.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.919-113C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/5 | chr11 | 134382137 | ||||||
chr11:134382146
|
T | A | 1 | a0001c0001t0034g0029 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.919-122A>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/5 | chr11 | 134382146 | ||||||
chr11:134382227
|
T | G | 11 | a0001c0001t0003g0070a0001c0001t0008g0008a0001c0001t0008g0105others(8): Show | 12 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(9): Show |
intron_variant | MODIFIER | c.919-203A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/5 | chr11 | 134382227 | ||||||
chr11:134382233
|
G | A | 1 | a0001c0001t0001g0163 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.919-209C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/5 | chr11 | 134382233 | ||||||
chr11:134382244
|
G | A | 8 | a0001c0001t0013g0297a0001c0001t0013g0317a0001c0001t0013g0318others(5): Show | 8 | HG01496.hp2 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.919-220C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/5 | chr11 | 134382244 | ||||||
chr11:134382269
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.919-245G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/5 | chr11 | 134382269 | ||||||
chr11:134382286
|
A | G | 1 | a0001c0001t0005g0310 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.919-262T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/5 | chr11 | 134382286 | ||||||
chr11:134382306
|
A | AGT | 92 | a0001c0001t0001g0006a0001c0001t0001g0063a0001c0001t0001g0068others(89): Show | 96 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.919-284_919-283dup others(2): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/5 | chr11 | 134382306 | ||||||
chr11:134382306
|
A | AGTGT | 146 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(143): Show | 154 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.919-286_919-283dup others(4): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/5 | chr11 | 134382306 | ||||||
chr11:134382325
|
G | A | 6 | a0001c0001t0001g0224a0001c0001t0002g0323a0001c0001t0002g0324others(3): Show | 6 | HG01081.hp2 HG01891.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.919-301C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/5 | chr11 | 134382325 | ||||||
chr11:134382362
|
T | C | 17 | a0001c0001t0001g0005a0001c0001t0001g0067a0001c0001t0001g0071others(14): Show | 18 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(15): Show |
intron_variant | MODIFIER | c.919-338A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/5 | chr11 | 134382362 | ||||||
chr11:134382377
|
C | G | 20 | a0001c0001t0001g0172a0001c0001t0001g0174a0001c0001t0010g0004others(17): Show | 21 | HG01168.hp2 HG01169.hp1 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.918+333G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/5 | chr11 | 134382377 | ||||||
chr11:134382409
|
ATG | A | 227 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(224): Show | 239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.918+299_918+300del others(2): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/5 | chr11 | 134382409 | ||||||
chr11:134382418
|
T | C | 1 | a0001c0001t0003g0070 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.918+292A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/5 | chr11 | 134382418 | ||||||
chr11:134382452
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.918+258A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/5 | chr11 | 134382452 | ||||||
chr11:134382527
|
T | G | 6 | a0001c0001t0001g0224a0001c0001t0002g0323a0001c0001t0002g0324others(3): Show | 6 | HG01081.hp2 HG01891.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.918+183A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/5 | chr11 | 134382527 | ||||||
chr11:134382571
|
A | G | 1 | a0001c0001t0053g0321 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.918+139T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/5 | chr11 | 134382571 | ||||||
chr11:134382707
|
C | A | 1 | a0001c0001t0014g0053 | 1 | NA19000.hp2 | splice_region_variant&intron_variant | LOW | c.918+3G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/5 | chr11 | 134382707 | ||||||
chr11:134383012
|
A | AG | 21 | a0001c0001t0002g0284a0001c0001t0010g0004a0001c0001t0010g0061others(18): Show | 22 | HG01168.hp2 HG01169.hp1 HG01358.hp1 others(19): Show |
splice_region_variant&intron_variant | LOW | c.622-7dupC | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 3/5 | chr11 | 134383012 | ||||||
chr11:134383118
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.622-112G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 3/5 | chr11 | 134383118 | ||||||
chr11:134383159
|
G | A | 1 | a0001c0001t0005g0320 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.622-153C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 3/5 | chr11 | 134383159 | ||||||
chr11:134383335
|
G | C | 9 | a0001c0001t0008g0008a0001c0001t0008g0105a0001c0001t0008g0117others(6): Show | 10 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.622-329C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 3/5 | chr11 | 134383335 | ||||||
chr11:134383462
|
T | C | 1 | a0001c0001t0046g0245 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.621+218A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 3/5 | chr11 | 134383462 | ||||||
chr11:134383512
|
A | C | 1 | a0001c0001t0001g0132 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.621+168T>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 3/5 | chr11 | 134383512 | ||||||
chr11:134383669
|
C | A | 1 | a0001c0003t0004g0267 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.621+11G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 3/5 | chr11 | 134383669 | ||||||
chr11:134384252
|
G | A | 2 | a0001c0001t0001g0010a0001c0001t0006g0047 | 3 | HG00738.hp2 HG01069.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.113-64C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134384252 | ||||||
chr11:134384455
|
C | T | 1 | a0001c0001t0002g0313 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.113-267G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134384455 | ||||||
chr11:134384467
|
A | G | 1 | a0001c0001t0001g0116 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.113-279T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134384467 | ||||||
chr11:134384496
|
C | A | 7 | a0001c0001t0004g0248a0001c0001t0012g0263a0001c0003t0001g0235others(4): Show | 7 | HG02258.hp2 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.113-308G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134384496 | ||||||
chr11:134384530
|
C | T | 2 | a0001c0001t0001g0146a0001c0001t0001g0205 | 2 | HG00673.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.113-342G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134384530 | ||||||
chr11:134384558
|
G | A | 1 | a0001c0003t0048g0268 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.113-370C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134384558 | ||||||
chr11:134384564
|
C | T | 1 | a0001c0001t0011g0031 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.113-376G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134384564 | ||||||
chr11:134384902
|
C | T | 80 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0067others(77): Show | 85 | HG00323.hp2 HG00408.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.113-714G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134384902 | ||||||
chr11:134384919
|
T | C | 3 | a0002c0002t0001g0190a0002c0002t0001g0194a0002c0002t0001g0229 | 3 | HG01891.hp2 HG02622.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.113-731A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134384919 | ||||||
chr11:134384945
|
T | C | 336 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(333): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.113-757A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134384945 | ||||||
chr11:134385137
|
C | A | 1 | a0001c0001t0047g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.113-949G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134385137 | ||||||
chr11:134385140
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.113-952C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134385140 | ||||||
chr11:134385295
|
G | T | 54 | a0001c0001t0001g0005a0001c0001t0001g0062a0001c0001t0001g0064others(51): Show | 55 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.113-1107C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134385295 | ||||||
chr11:134385299
|
T | C | 1 | a0001c0003t0001g0235 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.113-1111A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134385299 | ||||||
chr11:134385350
|
T | C | 258 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(255): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.113-1162A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134385350 | ||||||
chr11:134385431
|
T | C | 79 | a0001c0001t0001g0007a0001c0001t0001g0062a0001c0001t0001g0063others(76): Show | 86 | HG00280.hp2 HG00544.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.113-1243A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134385431 | ||||||
chr11:134385496
|
G | A | 1 | a0001c0001t0003g0070 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.113-1308C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134385496 | ||||||
chr11:134385496
|
G | C | 40 | a0001c0001t0001g0010a0001c0001t0001g0217a0001c0001t0001g0224others(37): Show | 43 | HG00639.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.113-1308C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134385496 | ||||||
chr11:134385504
|
T | C | 2 | a0001c0001t0031g0026a0001c0001t0054g0285 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.113-1316A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134385504 | ||||||
chr11:134385543
|
C | G | 2 | a0001c0001t0005g0327a0001c0001t0007g0231 | 2 | HG03239.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.113-1355G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134385543 | ||||||
chr11:134385555
|
C | T | 32 | a0001c0001t0001g0137a0001c0001t0001g0148a0001c0001t0003g0060others(29): Show | 34 | HG00642.hp1 HG01074.hp2 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.113-1367G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134385555 | ||||||
chr11:134385558
|
GATGGGTG others(39): Show |
G | 5 | a0001c0001t0002g0322a0001c0001t0003g0195a0001c0001t0012g0265others(2): Show | 5 | HG01243.hp2 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.113-1416_113-1371d others(48): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134385558 | ||||||
chr11:134385570
|
G | C | 218 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(215): Show | 228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.113-1382C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134385570 | ||||||
chr11:134385703
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.113-1515G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134385703 | ||||||
chr11:134385717
|
C | T | 1 | a0001c0001t0001g0065 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.113-1529G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134385717 | ||||||
chr11:134385764
|
C | T | 3 | a0001c0001t0003g0070a0001c0001t0045g0223a0001c0003t0048g0268 | 3 | HG02145.hp2 HG02559.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.113-1576G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134385764 | ||||||
chr11:134385765
|
G | A | 1 | a0001c0001t0045g0223 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.113-1577C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134385765 | ||||||
chr11:134385940
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.112+1608A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134385940 | ||||||
chr11:134386034
|
CAAGATAA others(5): Show |
C | 1 | a0001c0001t0001g0167 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.112+1502_112+1513d others(14): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134386034 | ||||||
chr11:134386085
|
C | T | 21 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0106others(18): Show | 22 | HG00408.hp1 HG00639.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.112+1463G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134386085 | ||||||
chr11:134386147
|
C | G | 1 | a0001c0001t0013g0318 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.112+1401G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134386147 | ||||||
chr11:134386412
|
A | G | 1 | a0001c0001t0001g0167 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.112+1136T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134386412 | ||||||
chr11:134386413
|
G | A | 1 | a0001c0001t0001g0167 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.112+1135C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134386413 | ||||||
chr11:134386423
|
A | AAG | 312 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(309): Show | 325 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(322): Show |
intron_variant | MODIFIER | c.112+1123_112+1124d others(4): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134386423 | ||||||
chr11:134386729
|
G | T | 1 | a0001c0003t0004g0251 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.112+819C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134386729 | ||||||
chr11:134386857
|
A | G | 20 | a0001c0001t0004g0248a0001c0001t0044g0057a0001c0003t0004g0249others(17): Show | 20 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.112+691T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134386857 | ||||||
chr11:134386887
|
C | G | 145 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(142): Show | 151 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.112+661G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134386887 | ||||||
chr11:134386911
|
C | T | 23 | a0001c0001t0001g0063a0001c0001t0001g0068a0001c0001t0001g0160others(20): Show | 24 | HG01243.hp2 HG01256.hp1 HG01257.hp1 others(21): Show |
intron_variant | MODIFIER | c.112+637G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134386911 | ||||||
chr11:134386925
|
C | A | 14 | a0002c0002t0001g0082a0002c0002t0001g0190a0002c0002t0001g0194others(11): Show | 14 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.112+623G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134386925 | ||||||
chr11:134386929
|
C | A | 1 | a0001c0001t0004g0252 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.112+619G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134386929 | ||||||
chr11:134386960
|
T | G | 6 | a0001c0001t0004g0248a0001c0001t0044g0057a0001c0003t0004g0249others(3): Show | 6 | HG02572.hp1 HG02717.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.112+588A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134386960 | ||||||
chr11:134387008
|
C | G | 1 | a0001c0001t0001g0208 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.112+540G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134387008 | ||||||
chr11:134387021
|
G | A | 1 | a0001c0001t0008g0161 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.112+527C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134387021 | ||||||
chr11:134387126
|
G | A | 3 | a0001c0001t0004g0255a0001c0001t0014g0055a0001c0003t0048g0268 | 3 | HG02717.hp1 NA19011.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.112+422C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134387126 | ||||||
chr11:134387184
|
C | G | 23 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0106others(20): Show | 24 | HG00408.hp1 HG00639.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.112+364G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134387184 | ||||||
chr11:134387458
|
G | C | 1 | a0001c0001t0047g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.112+90C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134387458 | ||||||
chr11:134388078
|
T | C | 5 | a0001c0001t0004g0001a0001c0001t0004g0260a0001c0001t0004g0261others(2): Show | 7 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-281-138A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134388078 | ||||||
chr11:134388248
|
A | C | 20 | a0001c0001t0004g0248a0001c0001t0044g0057a0001c0003t0004g0249others(17): Show | 20 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-281-308T>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134388248 | ||||||
chr11:134388297
|
A | G | 6 | a0001c0001t0004g0001a0001c0001t0004g0260a0001c0001t0004g0261others(3): Show | 8 | HG02109.hp1 HG02809.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-281-357T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134388297 | ||||||
chr11:134388351
|
G | A | 1 | a0001c0001t0003g0186 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-281-411C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134388351 | ||||||
chr11:134388429
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-281-489G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134388429 | ||||||
chr11:134388430
|
T | C | 1 | a0001c0001t0001g0167 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-281-490A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134388430 | ||||||
chr11:134388503
|
T | C | 1 | a0001c0001t0003g0222 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-281-563A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134388503 | ||||||
chr11:134388522
|
T | G | 271 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(268): Show | 282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.-281-582A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134388522 | ||||||
chr11:134388779
|
C | T | 22 | a0001c0001t0004g0248a0001c0001t0044g0057a0001c0001t0045g0223others(19): Show | 22 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.-281-839G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134388779 | ||||||
chr11:134388838
|
T | C | 1 | a0001c0001t0001g0214 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-281-898A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134388838 | ||||||
chr11:134389055
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-281-1115T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134389055 | ||||||
chr11:134389519
|
C | T | 5 | a0001c0001t0004g0001a0001c0001t0004g0260a0001c0001t0004g0261others(2): Show | 7 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-281-1579G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134389519 | ||||||
chr11:134389617
|
G | A | 1 | a0001c0001t0003g0203 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-281-1677C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134389617 | ||||||
chr11:134389664
|
A | G | 334 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(331): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.-281-1724T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134389664 | ||||||
chr11:134389669
|
G | C | 41 | a0001c0001t0001g0063a0001c0001t0001g0068a0001c0001t0001g0145others(38): Show | 42 | HG00438.hp1 HG00544.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.-281-1729C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134389669 | ||||||
chr11:134389732
|
T | C | 4 | a0001c0001t0010g0004a0001c0001t0019g0033a0001c0001t0031g0026others(1): Show | 5 | HG01168.hp2 HG01169.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.-281-1792A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134389732 | ||||||
chr11:134389826
|
G | A | 8 | a0001c0001t0004g0001a0001c0001t0004g0252a0001c0001t0004g0260others(5): Show | 10 | HG02109.hp1 HG02451.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.-281-1886C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134389826 | ||||||
chr11:134389931
|
G | A | 2 | a0001c0001t0010g0189a0001c0001t0047g0247 | 2 | HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-281-1991C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134389931 | ||||||
chr11:134390032
|
C | A | 8 | a0001c0001t0004g0001a0001c0001t0004g0252a0001c0001t0004g0260others(5): Show | 10 | HG02109.hp1 HG02451.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.-281-2092G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134390032 | ||||||
chr11:134390087
|
GTT | G | 79 | a0001c0001t0001g0063a0001c0001t0001g0068a0001c0001t0001g0114others(76): Show | 83 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.-281-2149_-281-214 others(6): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134390087 | ||||||
chr11:134390090
|
C | G | 79 | a0001c0001t0001g0063a0001c0001t0001g0068a0001c0001t0001g0114others(76): Show | 83 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.-281-2150G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134390090 | ||||||
chr11:134390091
|
C | A | 79 | a0001c0001t0001g0063a0001c0001t0001g0068a0001c0001t0001g0114others(76): Show | 83 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.-281-2151G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134390091 | ||||||
chr11:134390092
|
C | G | 79 | a0001c0001t0001g0063a0001c0001t0001g0068a0001c0001t0001g0114others(76): Show | 83 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.-281-2152G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134390092 | ||||||
chr11:134390093
|
C | A | 79 | a0001c0001t0001g0063a0001c0001t0001g0068a0001c0001t0001g0114others(76): Show | 83 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.-281-2153G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134390093 | ||||||
chr11:134390132
|
G | C | 48 | a0001c0001t0001g0114a0001c0001t0001g0138a0001c0001t0001g0143others(45): Show | 49 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.-281-2192C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134390132 | ||||||
chr11:134390175
|
C | A | 34 | a0001c0001t0001g0114a0001c0001t0001g0138a0001c0001t0001g0143others(31): Show | 34 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.-281-2235G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134390175 | ||||||
chr11:134390283
|
C | T | 1 | a0001c0001t0010g0189 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-281-2343G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134390283 | ||||||
chr11:134390284
|
A | G | 40 | a0001c0001t0001g0114a0001c0001t0001g0138a0001c0001t0001g0143others(37): Show | 42 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.-281-2344T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134390284 | ||||||
chr11:134390350
|
C | G | 6 | a0001c0001t0004g0001a0001c0001t0004g0260a0001c0001t0004g0261others(3): Show | 8 | HG02109.hp1 HG02809.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-281-2410G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134390350 | ||||||
chr11:134390410
|
T | TCTTCTCA others(3): Show |
1 | a0001c0001t0001g0167 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-281-2471_-281-247 others(14): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134390410 | ||||||
chr11:134390411
|
T | A | 1 | a0001c0001t0001g0167 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-281-2471A>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134390411 | ||||||
chr11:134390425
|
G | T | 1 | a0001c0001t0007g0199 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-281-2485C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134390425 | ||||||
chr11:134390500
|
G | A | 14 | a0001c0001t0001g0224a0001c0001t0002g0323a0001c0001t0002g0324others(11): Show | 15 | HG01081.hp2 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-281-2560C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134390500 | ||||||
chr11:134390739
|
C | G | 1 | a0001c0003t0048g0268 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-281-2799G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134390739 | ||||||
chr11:134390995
|
C | T | 13 | a0001c0001t0001g0006a0001c0001t0001g0087a0001c0001t0001g0088others(10): Show | 14 | HG00099.hp1 HG00140.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.-281-3055G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134390995 | ||||||
chr11:134391018
|
T | C | 36 | a0001c0001t0001g0224a0001c0001t0002g0323a0001c0001t0002g0324others(33): Show | 38 | HG00438.hp1 HG01074.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.-281-3078A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134391018 | ||||||
chr11:134391040
|
C | T | 5 | a0001c0001t0002g0298a0001c0001t0003g0115a0001c0001t0003g0126others(2): Show | 5 | HG01123.hp1 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.-281-3100G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134391040 | ||||||
chr11:134391236
|
C | G | 1 | a0001c0001t0047g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-281-3296G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134391236 | ||||||
chr11:134391256
|
A | G | 56 | a0001c0001t0001g0063a0001c0001t0001g0068a0001c0001t0002g0322others(53): Show | 59 | HG00438.hp1 HG01074.hp2 HG01243.hp1 others(56): Show |
intron_variant | MODIFIER | c.-281-3316T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134391256 | ||||||
chr11:134391329
|
T | C | 28 | a0001c0001t0004g0001a0001c0001t0004g0248a0001c0001t0004g0260others(25): Show | 30 | HG00438.hp1 HG01074.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.-281-3389A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134391329 | ||||||
chr11:134391412
|
C | T | 1 | a0001c0003t0048g0268 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-281-3472G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134391412 | ||||||
chr11:134391502
|
G | A | 11 | a0001c0001t0002g0322a0001c0001t0009g0240a0001c0001t0009g0241others(8): Show | 11 | HG01243.hp2 HG02015.hp2 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.-281-3562C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134391502 | ||||||
chr11:134391531
|
T | C | 1 | a0001c0001t0012g0265 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-281-3591A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134391531 | ||||||
chr11:134391627
|
C | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0079 | 2 | HG00280.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.-281-3687G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134391627 | ||||||
chr11:134391682
|
G | A | 3 | a0001c0001t0001g0173a0001c0001t0006g0043a0001c0001t0006g0044 | 3 | HG00735.hp2 HG00741.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-281-3742C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134391682 | ||||||
chr11:134391698
|
C | T | 1 | a0001c0001t0001g0006 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-281-3758G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134391698 | ||||||
chr11:134391814
|
A | T | 1 | a0001c0001t0004g0252 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-281-3874T>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134391814 | ||||||
chr11:134391879
|
T | G | 21 | a0001c0001t0004g0248a0001c0001t0044g0057a0001c0003t0004g0249others(18): Show | 21 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.-281-3939A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134391879 | ||||||
chr11:134391889
|
A | T | 1 | a0001c0001t0003g0149 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-281-3949T>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134391889 | ||||||
chr11:134391938
|
G | A | 1 | a0001c0001t0011g0038 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-281-3998C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134391938 | ||||||
chr11:134391951
|
T | G | 5 | a0001c0001t0004g0001a0001c0001t0004g0260a0001c0001t0004g0261others(2): Show | 7 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-281-4011A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134391951 | ||||||
chr11:134392018
|
C | T | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-281-4078G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134392018 | ||||||
chr11:134392100
|
C | T | 2 | a0001c0001t0001g0204a0001c0001t0005g0316 | 2 | HG00438.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-281-4160G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134392100 | ||||||
chr11:134392151
|
A | G | 1 | a0001c0003t0048g0268 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-281-4211T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134392151 | ||||||
chr11:134392189
|
T | TCCGTGGA others(27): Show |
22 | a0001c0001t0004g0248a0001c0001t0044g0057a0001c0001t0047g0247others(19): Show | 22 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.-281-4283_-281-425 others(38): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134392189 | ||||||
chr11:134392260
|
A | G | 70 | a0001c0001t0001g0063a0001c0001t0001g0068a0001c0001t0001g0224others(67): Show | 74 | HG00438.hp1 HG01074.hp2 HG01081.hp2 others(71): Show |
intron_variant | MODIFIER | c.-281-4320T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134392260 | ||||||
chr11:134392260
|
ATGGAACT others(21): Show |
A | 1 | a0001c0001t0040g0150 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-281-4348_-281-432 others(32): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134392260 | ||||||
chr11:134392340
|
C | G | 1 | a0001c0001t0001g0064 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-281-4400G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134392340 | ||||||
chr11:134392444
|
T | A | 212 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(209): Show | 221 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.-281-4504A>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134392444 | ||||||
chr11:134392461
|
C | T | 6 | a0001c0001t0004g0001a0001c0001t0004g0260a0001c0001t0004g0261others(3): Show | 8 | HG01106.hp1 HG02109.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-281-4521G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134392461 | ||||||
chr11:134392468
|
C | G | 21 | a0001c0001t0004g0248a0001c0001t0044g0057a0001c0003t0004g0249others(18): Show | 21 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.-281-4528G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134392468 | ||||||
chr11:134392639
|
G | A | 6 | a0001c0001t0004g0264a0001c0001t0010g0004a0001c0001t0012g0263others(3): Show | 7 | HG01168.hp2 HG01169.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.-281-4699C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134392639 | ||||||
chr11:134392674
|
G | A | 23 | a0001c0001t0004g0248a0001c0001t0005g0316a0001c0001t0044g0057others(20): Show | 23 | HG00438.hp1 HG01074.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.-281-4734C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134392674 | ||||||
chr11:134392676
|
A | G | 1 | a0001c0001t0003g0176 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-281-4736T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134392676 | ||||||
chr11:134392705
|
C | G | 42 | a0001c0001t0001g0224a0001c0001t0002g0323a0001c0001t0002g0324others(39): Show | 45 | HG00438.hp1 HG01074.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.-281-4765G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134392705 | ||||||
chr11:134392706
|
G | A | 1 | a0001c0001t0037g0048 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-281-4766C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134392706 | ||||||
chr11:134392947
|
T | A | 5 | a0001c0001t0004g0001a0001c0001t0004g0260a0001c0001t0004g0261others(2): Show | 7 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-281-5007A>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134392947 | ||||||
chr11:134393044
|
T | G | 2 | a0001c0001t0001g0201a0001c0001t0001g0218 | 2 | NA18952.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.-281-5104A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134393044 | ||||||
chr11:134393081
|
C | T | 1 | a0001c0001t0005g0316 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-281-5141G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134393081 | ||||||
chr11:134393434
|
C | G | 1 | a0001c0001t0010g0061 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-281-5494G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134393434 | ||||||
chr11:134393444
|
C | T | 1 | a0001c0001t0004g0252 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-281-5504G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134393444 | ||||||
chr11:134393522
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-281-5582G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134393522 | ||||||
chr11:134393776
|
C | T | 1 | a0001c0001t0019g0049 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-281-5836G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134393776 | ||||||
chr11:134393792
|
C | T | 10 | a0001c0001t0001g0006a0001c0001t0001g0087a0001c0001t0001g0088others(7): Show | 11 | HG00099.hp1 HG00140.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.-281-5852G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134393792 | ||||||
chr11:134393831
|
C | T | 1 | a0001c0001t0001g0212 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-281-5891G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134393831 | ||||||
chr11:134393834
|
C | A | 15 | a0001c0001t0001g0063a0001c0001t0002g0322a0001c0001t0004g0011others(12): Show | 16 | HG01243.hp2 HG01256.hp1 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-281-5894G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134393834 | ||||||
chr11:134393840
|
A | C | 15 | a0001c0001t0001g0063a0001c0001t0002g0322a0001c0001t0004g0011others(12): Show | 16 | HG01243.hp2 HG01256.hp1 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-281-5900T>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134393840 | ||||||
chr11:134393842
|
A | T | 7 | a0001c0001t0002g0323a0001c0001t0002g0324a0001c0001t0002g0325others(4): Show | 7 | HG01081.hp2 HG01891.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-281-5902T>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134393842 | ||||||
chr11:134393866
|
C | G | 6 | a0001c0001t0004g0001a0001c0001t0004g0260a0001c0001t0004g0261others(3): Show | 8 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-281-5926G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134393866 | ||||||
chr11:134393873
|
C | T | 6 | a0001c0001t0004g0001a0001c0001t0004g0260a0001c0001t0004g0261others(3): Show | 8 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-281-5933G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134393873 | ||||||
chr11:134394087
|
G | A | 7 | a0001c0001t0002g0323a0001c0001t0002g0324a0001c0001t0002g0325others(4): Show | 7 | HG01081.hp2 HG01891.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-281-6147C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134394087 | ||||||
chr11:134394248
|
T | C | 58 | a0001c0001t0001g0063a0001c0001t0001g0160a0001c0001t0001g0224others(55): Show | 59 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(56): Show |
intron_variant | MODIFIER | c.-281-6308A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134394248 | ||||||
chr11:134394290
|
G | A | 1 | a0001c0001t0001g0188 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-281-6350C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134394290 | ||||||
chr11:134394306
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-281-6366G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134394306 | ||||||
chr11:134394319
|
C | T | 15 | a0001c0001t0001g0063a0001c0001t0002g0322a0001c0001t0004g0011others(12): Show | 16 | HG01243.hp2 HG01256.hp1 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-281-6379G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134394319 | ||||||
chr11:134394333
|
A | G | 32 | a0001c0001t0001g0063a0001c0001t0001g0224a0001c0001t0002g0322others(29): Show | 33 | HG01074.hp2 HG01243.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.-281-6393T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134394333 | ||||||
chr11:134394361
|
T | C | 31 | a0001c0001t0001g0063a0001c0001t0001g0224a0001c0001t0002g0322others(28): Show | 32 | HG01074.hp2 HG01243.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.-281-6421A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134394361 | ||||||
chr11:134394372
|
C | A | 1 | a0001c0001t0039g0221 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-281-6432G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134394372 | ||||||
chr11:134394557
|
C | T | 1 | a0001c0001t0001g0087 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-281-6617G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134394557 | ||||||
chr11:134394597
|
C | A | 22 | a0001c0001t0001g0160a0001c0001t0004g0248a0001c0001t0004g0252others(19): Show | 22 | HG02015.hp2 HG02056.hp2 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.-281-6657G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134394597 | ||||||
chr11:134394597
|
C | G | 1 | a0001c0001t0003g0076 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-281-6657G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134394597 | ||||||
chr11:134394612
|
T | G | 15 | a0001c0001t0001g0063a0001c0001t0002g0322a0001c0001t0004g0011others(12): Show | 16 | HG01243.hp2 HG01256.hp1 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-281-6672A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134394612 | ||||||
chr11:134394635
|
A | G | 16 | a0001c0001t0001g0063a0001c0001t0002g0322a0001c0001t0004g0011others(13): Show | 17 | HG01243.hp2 HG01256.hp1 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-281-6695T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134394635 | ||||||
chr11:134394690
|
C | T | 1 | a0001c0001t0023g0311 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-281-6750G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134394690 | ||||||
chr11:134394702
|
T | C | 22 | a0001c0001t0001g0063a0001c0001t0002g0322a0001c0001t0002g0323others(19): Show | 23 | HG01081.hp2 HG01243.hp2 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.-281-6762A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134394702 | ||||||
chr11:134394835
|
G | A | 15 | a0001c0001t0001g0063a0001c0001t0002g0322a0001c0001t0004g0011others(12): Show | 16 | HG01243.hp2 HG01256.hp1 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-281-6895C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134394835 | ||||||
chr11:134395063
|
A | C | 1 | a0001c0001t0001g0130 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-281-7123T>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134395063 | ||||||
chr11:134395066
|
T | A | 1 | a0001c0001t0047g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-281-7126A>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134395066 | ||||||
chr11:134395197
|
C | CT | 29 | a0001c0001t0001g0063a0001c0001t0002g0322a0001c0001t0002g0323others(26): Show | 30 | HG01081.hp2 HG01243.hp2 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.-281-7258dupA | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134395197 | ||||||
chr11:134395200
|
G | A | 2 | a0001c0001t0001g0146a0001c0001t0001g0205 | 2 | HG00673.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.-281-7260C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134395200 | ||||||
chr11:134395215
|
C | T | 14 | a0001c0001t0002g0323a0001c0001t0002g0324a0001c0001t0002g0325others(11): Show | 14 | HG01081.hp2 HG01891.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.-281-7275G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134395215 | ||||||
chr11:134395219
|
T | G | 1 | a0001c0001t0042g0181 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-281-7279A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134395219 | ||||||
chr11:134395227
|
C | T | 29 | a0001c0001t0001g0063a0001c0001t0002g0322a0001c0001t0002g0323others(26): Show | 30 | HG01081.hp2 HG01243.hp2 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.-281-7287G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134395227 | ||||||
chr11:134395279
|
C | T | 23 | a0001c0001t0001g0063a0001c0001t0002g0322a0001c0001t0002g0323others(20): Show | 24 | HG01081.hp2 HG01243.hp2 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.-281-7339G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134395279 | ||||||
chr11:134395342
|
C | T | 22 | a0001c0001t0001g0063a0001c0001t0002g0322a0001c0001t0002g0323others(19): Show | 23 | HG01081.hp2 HG01243.hp2 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.-281-7402G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134395342 | ||||||
chr11:134395360
|
A | G | 22 | a0001c0001t0001g0063a0001c0001t0002g0322a0001c0001t0002g0323others(19): Show | 23 | HG01081.hp2 HG01243.hp2 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.-281-7420T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134395360 | ||||||
chr11:134395421
|
T | C | 22 | a0001c0001t0001g0063a0001c0001t0002g0322a0001c0001t0002g0323others(19): Show | 23 | HG01081.hp2 HG01243.hp2 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.-281-7481A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134395421 | ||||||
chr11:134395485
|
G | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0090a0001c0001t0001g0091others(2): Show | 6 | NA18948.hp1 NA18951.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.-281-7545C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134395485 | ||||||
chr11:134395643
|
C | G | 7 | a0001c0001t0002g0323a0001c0001t0002g0324a0001c0001t0002g0325others(4): Show | 7 | HG01081.hp2 HG01891.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-281-7703G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134395643 | ||||||
chr11:134395829
|
C | T | 15 | a0001c0001t0001g0063a0001c0001t0002g0322a0001c0001t0004g0011others(12): Show | 16 | HG01243.hp2 HG01256.hp1 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-281-7889G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134395829 | ||||||
chr11:134395895
|
T | C | 11 | a0001c0001t0001g0160a0001c0001t0005g0316a0001c0001t0009g0240others(8): Show | 11 | HG00438.hp1 HG02015.hp2 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.-281-7955A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134395895 | ||||||
chr11:134395964
|
G | A | 2 | a0001c0001t0005g0295a0001c0001t0015g0276 | 2 | HG01070.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-281-8024C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134395964 | ||||||
chr11:134396068
|
G | A | 9 | a0001c0001t0004g0248a0001c0001t0004g0252a0001c0001t0004g0269others(6): Show | 9 | HG02280.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-281-8128C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134396068 | ||||||
chr11:134396073
|
T | G | 35 | a0001c0001t0001g0063a0001c0001t0002g0322a0001c0001t0002g0323others(32): Show | 36 | HG01081.hp2 HG01243.hp2 HG01256.hp1 others(33): Show |
intron_variant | MODIFIER | c.-281-8133A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134396073 | ||||||
chr11:134396226
|
G | A | 2 | a0001c0001t0044g0057a0001c0003t0048g0268 | 2 | HG02717.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-281-8286C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134396226 | ||||||
chr11:134396350
|
G | A | 16 | a0001c0001t0001g0224a0001c0001t0010g0189a0001c0001t0045g0223others(13): Show | 16 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.-281-8410C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134396350 | ||||||
chr11:134396417
|
C | T | 1 | a0001c0001t0041g0096 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-281-8477G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134396417 | ||||||
chr11:134396455
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-281-8515C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134396455 | ||||||
chr11:134396478
|
A | G | 29 | a0001c0001t0001g0063a0001c0001t0002g0322a0001c0001t0002g0323others(26): Show | 30 | HG01081.hp2 HG01243.hp2 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.-281-8538T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134396478 | ||||||
chr11:134396624
|
GA | G | 33 | a0001c0001t0001g0075a0001c0001t0001g0156a0001c0001t0001g0167others(30): Show | 35 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-281-8685delT | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134396624 | ||||||
chr11:134396695
|
C | T | 1 | a0001c0001t0009g0244 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-281-8755G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134396695 | ||||||
chr11:134396722
|
G | A | 1 | a0001c0001t0009g0246 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-281-8782C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134396722 | ||||||
chr11:134396800
|
C | T | 5 | a0001c0001t0004g0001a0001c0001t0004g0260a0001c0001t0004g0261others(2): Show | 7 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-281-8860G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134396800 | ||||||
chr11:134396886
|
C | T | 1 | a0001c0001t0003g0094 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-281-8946G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134396886 | ||||||
chr11:134396898
|
C | T | 5 | a0001c0001t0004g0001a0001c0001t0004g0260a0001c0001t0004g0261others(2): Show | 7 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-281-8958G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134396898 | ||||||
chr11:134396901
|
C | T | 17 | a0001c0001t0002g0323a0001c0001t0002g0324a0001c0001t0002g0325others(14): Show | 17 | HG01081.hp2 HG01891.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-281-8961G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134396901 | ||||||
chr11:134396944
|
C | T | 2 | a0001c0001t0003g0094a0001c0001t0021g0095 | 2 | HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-281-9004G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134396944 | ||||||
chr11:134397014
|
C | T | 2 | a0001c0001t0008g0105a0001c0001t0008g0117 | 2 | HG00323.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.-281-9074G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397014 | ||||||
chr11:134397070
|
C | T | 1 | a0001c0001t0004g0252 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-281-9130G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397070 | ||||||
chr11:134397198
|
C | T | 15 | a0001c0001t0001g0063a0001c0001t0002g0322a0001c0001t0004g0011others(12): Show | 16 | HG01243.hp2 HG01256.hp1 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-281-9258G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397198 | ||||||
chr11:134397199
|
A | G | 71 | a0001c0001t0001g0063a0001c0001t0001g0075a0001c0001t0001g0224others(68): Show | 76 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(73): Show |
intron_variant | MODIFIER | c.-281-9259T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397199 | ||||||
chr11:134397278
|
C | T | 16 | a0001c0001t0001g0224a0001c0001t0010g0189a0001c0001t0045g0223others(13): Show | 16 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.-281-9338G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397278 | ||||||
chr11:134397347
|
G | A | 6 | a0001c0001t0005g0310a0001c0001t0005g0327a0001c0001t0005g0328others(3): Show | 6 | HG03130.hp2 HG03209.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.-281-9407C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397347 | ||||||
chr11:134397383
|
T | C | 22 | a0001c0001t0002g0323a0001c0001t0002g0324a0001c0001t0002g0325others(19): Show | 24 | HG01081.hp2 HG01891.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.-281-9443A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397383 | ||||||
chr11:134397391
|
C | T | 3 | a0001c0001t0001g0184a0001c0001t0007g0009a0001c0001t0007g0185 | 4 | HG01070.hp2 HG01071.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.-281-9451G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397391 | ||||||
chr11:134397397
|
T | TCTCCTGT others(3): Show |
17 | a0001c0001t0002g0323a0001c0001t0002g0324a0001c0001t0002g0325others(14): Show | 17 | HG01081.hp2 HG01891.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-281-9467_-281-945 others(14): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397397 | ||||||
chr11:134397410
|
G | A | 1 | a0001c0001t0007g0220 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-281-9470C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397410 | ||||||
chr11:134397424
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-281-9484G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397424 | ||||||
chr11:134397534
|
A | G | 17 | a0001c0001t0002g0323a0001c0001t0002g0324a0001c0001t0002g0325others(14): Show | 17 | HG01081.hp2 HG01891.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-281-9594T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397534 | ||||||
chr11:134397541
|
GCCAGAGG others(18): Show |
G | 16 | a0001c0001t0001g0077a0001c0001t0003g0076a0001c0001t0004g0001others(13): Show | 18 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.-281-9626_-281-960 others(29): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397541 | ||||||
chr11:134397623
|
G | T | 1 | a0001c0001t0005g0279 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-281-9683C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397623 | ||||||
chr11:134397653
|
G | A | 2 | a0001c0001t0008g0196a0001c0001t0008g0197 | 2 | HG01433.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-281-9713C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397653 | ||||||
chr11:134397653
|
G | T | 1 | a0001c0001t0001g0205 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-281-9713C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397653 | ||||||
chr11:134397744
|
C | T | 5 | a0001c0001t0004g0248a0001c0001t0044g0057a0001c0003t0004g0250others(2): Show | 5 | HG02717.hp2 HG02897.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-281-9804G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397744 | ||||||
chr11:134397790
|
C | T | 1 | a0001c0003t0048g0268 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-281-9850G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397790 | ||||||
chr11:134397832
|
C | T | 8 | a0001c0001t0002g0323a0001c0001t0002g0324a0001c0001t0002g0325others(5): Show | 8 | HG01081.hp2 HG01891.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-281-9892G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397832 | ||||||
chr11:134397876
|
G | A | 1 | a0001c0001t0047g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-281-9936C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397876 | ||||||
chr11:134397938
|
C | T | 1 | a0001c0001t0004g0269 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-281-9998G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397938 | ||||||
chr11:134397953
|
T | C | 1 | a0001c0001t0001g0112 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-281-10013A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397953 | ||||||
chr11:134398038
|
C | T | 1 | a0001c0001t0010g0189 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-281-10098G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134398038 | ||||||
chr11:134398155
|
ACACC | A | 5 | a0001c0001t0004g0001a0001c0001t0004g0260a0001c0001t0004g0261others(2): Show | 7 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-281-10219_-281-10 others(10): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134398155 | ||||||
chr11:134398201
|
C | T | 5 | a0001c0001t0002g0323a0001c0001t0002g0324a0001c0001t0002g0325others(2): Show | 5 | HG01081.hp2 HG01891.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-281-10261G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134398201 | ||||||
chr11:134398216
|
C | T | 18 | a0001c0001t0001g0063a0001c0001t0001g0188a0001c0001t0002g0322others(15): Show | 19 | HG01243.hp2 HG01256.hp1 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.-281-10276G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134398216 | ||||||
chr11:134398367
|
A | G | 2 | a0001c0001t0004g0264a0001c0001t0012g0263 | 2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-281-10427T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134398367 | ||||||
chr11:134398379
|
A | G | 5 | a0001c0001t0004g0001a0001c0001t0004g0260a0001c0001t0004g0261others(2): Show | 7 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-281-10439T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134398379 | ||||||
chr11:134398502
|
G | T | 1 | a0001c0003t0004g0250 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-281-10562C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134398502 | ||||||
chr11:134398517
|
T | C | 24 | a0001c0001t0001g0063a0001c0001t0001g0188a0001c0001t0002g0315others(21): Show | 25 | HG00099.hp2 HG01106.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.-281-10577A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134398517 | ||||||
chr11:134398559
|
T | C | 21 | a0001c0001t0001g0063a0001c0001t0002g0322a0001c0001t0004g0011others(18): Show | 22 | HG01243.hp2 HG01256.hp1 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.-281-10619A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134398559 | ||||||
chr11:134398559
|
T | TACAGATG others(71): Show |
5 | a0001c0001t0004g0001a0001c0001t0004g0260a0001c0001t0004g0261others(2): Show | 7 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-281-10620_-281-10 others(84): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134398559 | ||||||
chr11:134398593
|
G | A | 1 | a0001c0001t0003g0177 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-281-10653C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134398593 | ||||||
chr11:134398615
|
G | A | 15 | a0001c0001t0001g0137a0001c0001t0002g0277a0001c0001t0002g0292others(12): Show | 15 | HG01496.hp2 HG02559.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.-281-10675C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134398615 | ||||||
chr11:134398740
|
C | T | 44 | a0001c0001t0001g0063a0001c0001t0001g0224a0001c0001t0002g0322others(41): Show | 47 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.-281-10800G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134398740 | ||||||
chr11:134398758
|
C | G | 1 | a0001c0001t0005g0302 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-281-10818G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134398758 | ||||||
chr11:134398947
|
A | C | 6 | a0001c0001t0004g0001a0001c0001t0004g0260a0001c0001t0004g0261others(3): Show | 8 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-281-11007T>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134398947 | ||||||
chr11:134399197
|
T | C | 45 | a0001c0001t0001g0063a0001c0001t0001g0193a0001c0001t0001g0224others(42): Show | 48 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.-281-11257A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134399197 | ||||||
chr11:134399198
|
G | A | 2 | a0001c0001t0004g0255a0001c0001t0014g0055 | 2 | NA19011.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-281-11258C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134399198 | ||||||
chr11:134399212
|
G | A | 1 | a0001c0001t0003g0126 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-281-11272C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134399212 | ||||||
chr11:134399226
|
G | A | 22 | a0001c0001t0001g0063a0001c0001t0002g0312a0001c0001t0002g0314others(19): Show | 25 | HG01243.hp2 HG01256.hp1 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.-281-11286C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134399226 | ||||||
chr11:134399439
|
C | T | 2 | a0001c0001t0001g0215a0001c0001t0001g0216 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-281-11499G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134399439 | ||||||
chr11:134399689
|
C | G | 1 | a0001c0001t0002g0306 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-281-11749G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134399689 | ||||||
chr11:134399717
|
G | A | 1 | a0001c0001t0013g0317 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-281-11777C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134399717 | ||||||
chr11:134399743
|
C | T | 212 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(209): Show | 222 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.-281-11803G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134399743 | ||||||
chr11:134399878
|
G | C | 27 | a0001c0001t0001g0063a0001c0001t0002g0322a0001c0001t0002g0323others(24): Show | 30 | HG01081.hp2 HG01243.hp2 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.-282+11929C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134399878 | ||||||
chr11:134400109
|
C | T | 40 | a0001c0001t0001g0063a0001c0001t0001g0193a0001c0001t0001g0224others(37): Show | 43 | HG01074.hp2 HG01243.hp1 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.-282+11698G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134400109 | ||||||
chr11:134400171
|
C | A | 2 | a0001c0001t0004g0264a0001c0001t0012g0263 | 2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-282+11636G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134400171 | ||||||
chr11:134400176
|
A | G | 46 | a0001c0001t0001g0063a0001c0001t0001g0193a0001c0001t0001g0224others(43): Show | 49 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.-282+11631T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134400176 | ||||||
chr11:134400353
|
A | G | 1 | a0001c0001t0005g0310 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-282+11454T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134400353 | ||||||
chr11:134400387
|
T | A | 1 | a0001c0001t0004g0252 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-282+11420A>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134400387 | ||||||
chr11:134400440
|
C | T | 6 | a0001c0001t0002g0323a0001c0001t0002g0324a0001c0001t0002g0325others(3): Show | 6 | HG01081.hp2 HG01891.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-282+11367G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134400440 | ||||||
chr11:134400615
|
A | T | 6 | a0001c0001t0002g0323a0001c0001t0002g0324a0001c0001t0002g0325others(3): Show | 6 | HG01081.hp2 HG01891.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-282+11192T>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134400615 | ||||||
chr11:134400653
|
T | C | 3 | a0001c0001t0007g0089a0001c0001t0007g0199a0001c0001t0041g0096 | 3 | HG00544.hp1 HG00673.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.-282+11154A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134400653 | ||||||
chr11:134400666
|
G | A | 1 | a0001c0001t0005g0335 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-282+11141C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134400666 | ||||||
chr11:134400827
|
G | A | 40 | a0001c0001t0001g0063a0001c0001t0001g0193a0001c0001t0001g0224others(37): Show | 43 | HG01074.hp2 HG01243.hp1 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.-282+10980C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134400827 | ||||||
chr11:134400877
|
C | G | 1 | a0001c0001t0001g0111 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-282+10930G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134400877 | ||||||
chr11:134400974
|
G | A | 1 | a0001c0001t0007g0220 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-282+10833C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134400974 | ||||||
chr11:134401061
|
G | A | 45 | a0001c0001t0001g0063a0001c0001t0001g0193a0001c0001t0001g0224others(42): Show | 48 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.-282+10746C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134401061 | ||||||
chr11:134401128
|
C | T | 2 | a0001c0001t0004g0253a0001c0001t0014g0053 | 2 | NA19000.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-282+10679G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134401128 | ||||||
chr11:134401281
|
C | CAT | 19 | a0001c0001t0001g0193a0001c0001t0001g0224a0001c0001t0003g0191others(16): Show | 19 | HG01074.hp2 HG01243.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.-282+10524_-282+10 others(8): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134401281 | ||||||
chr11:134401393
|
G | A | 9 | a0001c0001t0001g0148a0001c0001t0003g0081a0001c0001t0003g0083others(6): Show | 9 | HG00642.hp1 HG01192.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-282+10414C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134401393 | ||||||
chr11:134401584
|
A | G | 1 | a0001c0001t0003g0165 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-282+10223T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134401584 | ||||||
chr11:134401751
|
T | A | 39 | a0001c0001t0001g0063a0001c0001t0001g0193a0001c0001t0001g0224others(36): Show | 42 | HG01074.hp2 HG01243.hp1 HG01256.hp1 others(39): Show |
intron_variant | MODIFIER | c.-282+10056A>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134401751 | ||||||
chr11:134401752
|
A | T | 9 | a0001c0001t0001g0128a0001c0001t0001g0142a0001c0001t0001g0147others(6): Show | 9 | HG01081.hp2 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-282+10055T>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134401752 | ||||||
chr11:134401771
|
C | T | 18 | a0001c0001t0001g0075a0001c0001t0002g0322a0001c0001t0007g0003others(15): Show | 20 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.-282+10036G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134401771 | ||||||
chr11:134401877
|
T | C | 39 | a0001c0001t0001g0063a0001c0001t0001g0193a0001c0001t0001g0224others(36): Show | 42 | HG01074.hp2 HG01243.hp1 HG01256.hp1 others(39): Show |
intron_variant | MODIFIER | c.-282+9930A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134401877 | ||||||
chr11:134401911
|
A | G | 39 | a0001c0001t0001g0063a0001c0001t0001g0193a0001c0001t0001g0224others(36): Show | 42 | HG01074.hp2 HG01243.hp1 HG01256.hp1 others(39): Show |
intron_variant | MODIFIER | c.-282+9896T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134401911 | ||||||
chr11:134401970
|
C | CG | 30 | a0001c0001t0001g0101a0001c0001t0001g0140a0001c0001t0001g0200others(27): Show | 31 | HG00408.hp1 HG00558.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.-282+9836dupC | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134401970 | ||||||
chr11:134401970
|
C | T | 1 | a0001c0001t0047g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-282+9837G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134401970 | ||||||
chr11:134401973
|
G | A | 2 | a0001c0001t0003g0136a0001c0001t0029g0020 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-282+9834C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134401973 | ||||||
chr11:134401978
|
GGC | G | 25 | a0001c0001t0001g0007a0001c0001t0001g0103a0001c0001t0001g0109others(22): Show | 27 | HG00140.hp2 HG00642.hp1 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.-282+9827_-282+982 others(6): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134401978 | ||||||
chr11:134401979
|
G | GT | 18 | a0001c0001t0001g0193a0001c0001t0001g0224a0001c0001t0003g0191others(15): Show | 18 | HG01074.hp2 HG01243.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-282+9827_-282+982 others(5): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134401979 | ||||||
chr11:134401979
|
G | T | 5 | a0001c0001t0004g0001a0001c0001t0004g0260a0001c0001t0004g0261others(2): Show | 7 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-282+9828C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134401979 | ||||||
chr11:134401979
|
GC | G | 92 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0064others(89): Show | 96 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.-282+9827delG | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134401979 | ||||||
chr11:134401980
|
C | G | 153 | a0001c0001t0001g0005a0001c0001t0001g0062a0001c0001t0001g0063others(150): Show | 159 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(156): Show |
intron_variant | MODIFIER | c.-282+9827G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134401980 | ||||||
chr11:134401982
|
G | A | 1 | a0001c0001t0001g0138 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-282+9825C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134401982 | ||||||
chr11:134401999
|
C | T | 20 | a0001c0001t0001g0063a0001c0001t0004g0001a0001c0001t0004g0011others(17): Show | 23 | HG01256.hp1 HG01257.hp1 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.-282+9808G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134401999 | ||||||
chr11:134402007
|
G | A | 1 | a0001c0001t0003g0060 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-282+9800C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134402007 | ||||||
chr11:134402160
|
T | A | 1 | a0001c0001t0003g0070 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-282+9647A>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134402160 | ||||||
chr11:134402250
|
G | A | 21 | a0001c0001t0001g0063a0001c0001t0004g0001a0001c0001t0004g0011others(18): Show | 24 | HG01256.hp1 HG01257.hp1 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.-282+9557C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134402250 | ||||||
chr11:134402268
|
G | A | 2 | a0001c0001t0004g0264a0001c0001t0012g0263 | 2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-282+9539C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134402268 | ||||||
chr11:134402316
|
G | C | 1 | a0001c0001t0003g0070 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-282+9491C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134402316 | ||||||
chr11:134402318
|
C | T | 1 | a0001c0001t0006g0034 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-282+9489G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134402318 | ||||||
chr11:134402355
|
C | T | 1 | a0001c0001t0013g0317 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-282+9452G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134402355 | ||||||
chr11:134402557
|
G | A | 39 | a0001c0001t0001g0063a0001c0001t0001g0193a0001c0001t0001g0224others(36): Show | 42 | HG01074.hp2 HG01243.hp1 HG01256.hp1 others(39): Show |
intron_variant | MODIFIER | c.-282+9250C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134402557 | ||||||
chr11:134402735
|
AAACCCTG others(9): Show |
A | 1 | a0001c0001t0001g0123 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-282+9056_-282+907 others(20): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134402735 | ||||||
chr11:134402870
|
G | A | 2 | a0001c0001t0033g0028a0001c0001t0043g0100 | 2 | HG03688.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-282+8937C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134402870 | ||||||
chr11:134402911
|
TC | T | 31 | a0001c0001t0001g0063a0001c0001t0001g0193a0001c0001t0001g0224others(28): Show | 32 | HG01074.hp2 HG01243.hp1 HG01257.hp1 others(29): Show |
intron_variant | MODIFIER | c.-282+8895delG | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134402911 | ||||||
chr11:134402911
|
TCA | T | 7 | a0001c0001t0004g0001a0001c0001t0004g0260a0001c0001t0004g0261others(4): Show | 9 | HG02109.hp1 HG02809.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.-282+8894_-282+889 others(6): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134402911 | ||||||
chr11:134402912
|
C | A | 1 | a0001c0001t0022g0257 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-282+8895G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134402912 | ||||||
chr11:134402912
|
CA | C | 8 | a0001c0001t0001g0211a0001c0001t0002g0323a0001c0001t0002g0324others(5): Show | 8 | HG01081.hp2 HG01891.hp1 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.-282+8894delT | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134402912 | ||||||
chr11:134403107
|
C | CACA | 4 | a0001c0001t0012g0265a0001c0001t0012g0266a0001c0001t0012g0270others(1): Show | 4 | HG02258.hp2 HG02723.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-282+8697_-282+869 others(7): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403107 | ||||||
chr11:134403139
|
G | A | 6 | a0001c0001t0002g0323a0001c0001t0002g0324a0001c0001t0002g0325others(3): Show | 6 | HG01081.hp2 HG01891.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-282+8668C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403139 | ||||||
chr11:134403150
|
G | A | 4 | a0001c0001t0003g0058a0001c0001t0003g0059a0001c0001t0003g0149others(1): Show | 4 | HG01255.hp1 HG03516.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-282+8657C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403150 | ||||||
chr11:134403200
|
G | A | 1 | a0001c0001t0047g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-282+8607C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403200 | ||||||
chr11:134403256
|
C | T | 3 | a0001c0001t0002g0325a0001c0001t0002g0326a0001c0001t0002g0333 | 3 | HG01891.hp1 HG02280.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-282+8551G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403256 | ||||||
chr11:134403265
|
T | A | 1 | a0001c0001t0001g0154 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-282+8542A>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403265 | ||||||
chr11:134403272
|
C | T | 1 | a0001c0001t0008g0161 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-282+8535G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403272 | ||||||
chr11:134403273
|
G | A | 1 | a0001c0001t0004g0252 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-282+8534C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403273 | ||||||
chr11:134403327
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-282+8480G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403327 | ||||||
chr11:134403385
|
C | T | 6 | a0001c0001t0002g0323a0001c0001t0002g0324a0001c0001t0002g0325others(3): Show | 6 | HG01081.hp2 HG01891.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-282+8422G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403385 | ||||||
chr11:134403410
|
A | G | 55 | a0001c0001t0001g0063a0001c0001t0001g0193a0001c0001t0001g0224others(52): Show | 58 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(55): Show |
intron_variant | MODIFIER | c.-282+8397T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403410 | ||||||
chr11:134403450
|
C | T | 1 | a0001c0001t0001g0155 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-282+8357G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403450 | ||||||
chr11:134403521
|
G | C | 1 | a0001c0001t0003g0070 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-282+8286C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403521 | ||||||
chr11:134403665
|
C | T | 73 | a0001c0001t0001g0063a0001c0001t0001g0075a0001c0001t0001g0193others(70): Show | 78 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(75): Show |
intron_variant | MODIFIER | c.-282+8142G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403665 | ||||||
chr11:134403742
|
G | A | 1 | a0002c0002t0002g0334 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-282+8065C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403742 | ||||||
chr11:134403847
|
A | G | 5 | a0001c0001t0001g0114a0001c0001t0001g0157a0001c0001t0001g0158others(2): Show | 5 | HG00639.hp2 HG01106.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.-282+7960T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403847 | ||||||
chr11:134403879
|
C | G | 1 | a0001c0001t0049g0271 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-282+7928G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403879 | ||||||
chr11:134403973
|
G | T | 38 | a0001c0001t0001g0063a0001c0001t0001g0193a0001c0001t0003g0191others(35): Show | 41 | HG01074.hp2 HG01243.hp1 HG01256.hp1 others(38): Show |
intron_variant | MODIFIER | c.-282+7834C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403973 | ||||||
chr11:134403977
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-282+7830G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403977 | ||||||
chr11:134403979
|
TTCTTTA | T | 5 | a0001c0001t0010g0189a0001c0001t0045g0223a0002c0002t0001g0190others(2): Show | 5 | HG01891.hp2 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-282+7822_-282+782 others(10): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403979 | ||||||
chr11:134403979
|
TTCTTTAT others(1): Show |
T | 4 | a0001c0001t0001g0193a0001c0001t0003g0192a0001c0001t0003g0195others(1): Show | 4 | HG01884.hp1 HG02615.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-282+7820_-282+782 others(12): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403979 | ||||||
chr11:134403979
|
TTCTTTAT others(3): Show |
T | 3 | a0001c0001t0003g0191a0002c0002t0006g0051a0002c0002t0016g0018 | 3 | HG02055.hp2 HG02258.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-282+7818_-282+782 others(14): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403979 | ||||||
chr11:134403979
|
TTCTTTAT others(5): Show |
T | 1 | a0002c0002t0001g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-282+7816_-282+782 others(16): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403979 | ||||||
chr11:134403979
|
TTCTTTAT others(17): Show |
T | 5 | a0001c0001t0004g0001a0001c0001t0004g0260a0001c0001t0004g0261others(2): Show | 7 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-282+7804_-282+782 others(28): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403979 | ||||||
chr11:134403979
|
TTCTTTAT others(19): Show |
T | 2 | a0002c0002t0001g0227a0002c0002t0001g0228 | 2 | HG01243.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.-282+7802_-282+782 others(30): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403979 | ||||||
chr11:134403979
|
TTCTTTAT others(21): Show |
T | 4 | a0001c0001t0004g0011a0001c0001t0004g0255a0001c0001t0014g0053others(1): Show | 5 | HG01257.hp1 HG01258.hp2 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.-282+7800_-282+782 others(32): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403979 | ||||||
chr11:134403979
|
TTCTTTAT others(23): Show |
T | 10 | a0001c0001t0001g0063a0001c0001t0004g0253a0001c0001t0004g0254others(7): Show | 10 | HG01256.hp1 HG01261.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.-282+7798_-282+782 others(34): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403979 | ||||||
chr11:134403979
|
TTCTTTAT others(25): Show |
T | 1 | a0001c0001t0047g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-282+7796_-282+782 others(36): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403979 | ||||||
chr11:134403981
|
C | A | 2 | a0002c0002t0001g0234a0002c0002t0006g0050 | 2 | HG01074.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-282+7826G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403981 | ||||||
chr11:134403981
|
CT | C | 4 | a0001c0001t0001g0124a0001c0001t0001g0169a0001c0001t0002g0314others(1): Show | 4 | HG00609.hp1 HG00642.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-282+7825delA | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403981 | ||||||
chr11:134403983
|
T | A | 7 | a0001c0001t0001g0208a0001c0001t0002g0314a0001c0001t0006g0032others(4): Show | 7 | HG01074.hp2 HG02630.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-282+7824A>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403983 | ||||||
chr11:134403983
|
T | TA | 3 | a0001c0001t0001g0077a0001c0001t0001g0187a0001c0001t0020g0139 | 3 | HG00438.hp2 HG02083.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-282+7823_-282+782 others(5): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403983 | ||||||
chr11:134403983
|
T | TTA | 42 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0068others(39): Show | 43 | HG00597.hp2 HG00621.hp1 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.-282+7822_-282+782 others(6): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403983 | ||||||
chr11:134403983
|
T | TTATA | 40 | a0001c0001t0001g0010a0001c0001t0001g0062a0001c0001t0001g0073others(37): Show | 43 | HG00408.hp2 HG00544.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.-282+7820_-282+782 others(8): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403983 | ||||||
chr11:134403983
|
T | TTATATA | 13 | a0001c0001t0001g0074a0001c0001t0001g0079a0001c0001t0001g0151others(10): Show | 13 | HG00280.hp2 HG00597.hp1 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.-282+7818_-282+782 others(10): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403983 | ||||||
chr11:134403983
|
T | TTATATAT others(1): Show |
3 | a0001c0001t0001g0160a0001c0001t0001g0212a0001c0001t0003g0084 | 3 | HG02074.hp1 NA18612.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-282+7816_-282+782 others(12): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403983 | ||||||
chr11:134403983
|
T | TTATATAT others(3): Show |
2 | a0001c0001t0001g0239a0001c0001t0027g0016 | 2 | HG00544.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-282+7814_-282+782 others(14): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403983 | ||||||
chr11:134403983
|
T | TTATATAT others(5): Show |
2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG00558.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.-282+7812_-282+782 others(16): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403983 | ||||||
chr11:134403983
|
T | TTATATAT others(9): Show |
1 | a0001c0001t0002g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-282+7808_-282+782 others(20): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403983 | ||||||
chr11:134403983
|
T | TTATATAT others(11): Show |
1 | a0001c0001t0002g0313 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-282+7806_-282+782 others(22): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403983 | ||||||
chr11:134403983
|
TTA | T | 32 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0090others(29): Show | 34 | HG00438.hp1 HG01123.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.-282+7822_-282+782 others(6): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403983 | ||||||
chr11:134403983
|
TTATA | T | 22 | a0001c0001t0001g0075a0001c0001t0001g0080a0001c0001t0001g0086others(19): Show | 23 | HG00323.hp2 HG00408.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.-282+7820_-282+782 others(8): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403983 | ||||||
chr11:134403983
|
TTATATA | T | 13 | a0001c0001t0001g0106a0001c0001t0001g0170a0001c0001t0001g0218others(10): Show | 13 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.-282+7818_-282+782 others(10): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403983 | ||||||
chr11:134403983
|
TTATATAT others(1): Show |
T | 16 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(13): Show | 16 | HG00099.hp2 HG01109.hp2 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.-282+7816_-282+782 others(12): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403983 | ||||||
chr11:134403983
|
TTATATAT others(3): Show |
T | 4 | a0001c0001t0003g0176a0001c0001t0003g0177a0001c0001t0004g0269others(1): Show | 4 | HG02698.hp1 HG02735.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-282+7814_-282+782 others(14): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403983 | ||||||
chr11:134403983
|
TTATATAT others(5): Show |
T | 8 | a0001c0001t0001g0163a0001c0001t0006g0034a0001c0001t0006g0041others(5): Show | 8 | HG00280.hp1 HG03017.hp1 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.-282+7812_-282+782 others(16): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403983 | ||||||
chr11:134403983
|
TTATATAT others(7): Show |
T | 6 | a0001c0001t0009g0240a0001c0001t0009g0244a0001c0001t0026g0015others(3): Show | 6 | HG02015.hp2 HG02056.hp2 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.-282+7810_-282+782 others(18): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403983 | ||||||
chr11:134403983
|
TTATATAT others(9): Show |
T | 4 | a0001c0001t0001g0099a0001c0001t0001g0236a0001c0001t0003g0222others(1): Show | 4 | HG00099.hp1 HG02717.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.-282+7808_-282+782 others(20): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403983 | ||||||
chr11:134403983
|
TTATATAT others(11): Show |
T | 1 | a0001c0001t0021g0056 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-282+7806_-282+782 others(22): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403983 | ||||||
chr11:134403983
|
TTATATAT others(25): Show |
T | 1 | a0001c0001t0005g0329 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-282+7792_-282+782 others(36): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403983 | ||||||
chr11:134403994
|
T | C | 1 | a0001c0001t0009g0243 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-282+7813A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403994 | ||||||
chr11:134403996
|
T | C | 2 | a0001c0001t0009g0241a0001c0001t0009g0242 | 2 | NA18954.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-282+7811A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403996 | ||||||
chr11:134403998
|
T | C | 6 | a0001c0001t0009g0240a0001c0001t0009g0244a0001c0001t0026g0015others(3): Show | 6 | HG02015.hp2 HG02056.hp2 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.-282+7809A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403998 | ||||||
chr11:134404019
|
A | T | 1 | a0001c0001t0004g0269 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-282+7788T>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404019 | ||||||
chr11:134404023
|
A | T | 2 | a0001c0001t0004g0269a0002c0002t0002g0334 | 2 | HG02280.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-282+7784T>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404023 | ||||||
chr11:134404027
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0039g0221 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-282+7779_-282+778 others(14): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404027 | ||||||
chr11:134404027
|
A | ATATATAT others(11): Show |
1 | a0001c0003t0004g0251 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-282+7779_-282+778 others(22): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404027 | ||||||
chr11:134404027
|
A | ATATATAT others(9): Show |
1 | a0001c0003t0004g0250 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-282+7779_-282+778 others(20): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404027 | ||||||
chr11:134404027
|
A | ATATATT | 3 | a0001c0001t0001g0217a0001c0001t0007g0098a0001c0001t0019g0049 | 3 | HG02080.hp2 HG03195.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-282+7779_-282+778 others(10): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404027 | ||||||
chr11:134404027
|
A | ATATTTAT others(5): Show |
1 | a0001c0003t0004g0249 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-282+7779_-282+778 others(16): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404027 | ||||||
chr11:134404027
|
A | ATT | 2 | a0001c0001t0010g0004a0001c0001t0019g0033 | 3 | HG01358.hp1 HG01952.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.-282+7779_-282+778 others(6): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404027 | ||||||
chr11:134404027
|
A | ATTTATTT others(3): Show |
1 | a0001c0001t0044g0057 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-282+7779_-282+778 others(14): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404027 | ||||||
chr11:134404027
|
A | T | 19 | a0001c0001t0001g0075a0001c0001t0004g0248a0001c0001t0004g0264others(16): Show | 20 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.-282+7780T>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404027 | ||||||
chr11:134404031
|
T | A | 11 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(8): Show | 11 | HG00609.hp1 HG00639.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.-282+7776A>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404031 | ||||||
chr11:134404039
|
C | T | 28 | a0001c0001t0001g0075a0001c0001t0002g0322a0001c0001t0004g0248others(25): Show | 30 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.-282+7768G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404039 | ||||||
chr11:134404040
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-282+7767C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404040 | ||||||
chr11:134404111
|
C | T | 23 | a0001c0001t0001g0075a0001c0001t0002g0322a0001c0001t0004g0252others(20): Show | 25 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.-282+7696G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404111 | ||||||
chr11:134404112
|
T | G | 66 | a0001c0001t0001g0063a0001c0001t0001g0075a0001c0001t0001g0193others(63): Show | 71 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(68): Show |
intron_variant | MODIFIER | c.-282+7695A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404112 | ||||||
chr11:134404113
|
G | A | 17 | a0001c0001t0001g0193a0001c0001t0001g0224a0001c0001t0003g0191others(14): Show | 17 | HG01074.hp2 HG01243.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.-282+7694C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404113 | ||||||
chr11:134404117
|
C | T | 66 | a0001c0001t0001g0063a0001c0001t0001g0075a0001c0001t0001g0193others(63): Show | 71 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(68): Show |
intron_variant | MODIFIER | c.-282+7690G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404117 | ||||||
chr11:134404275
|
G | GT | 18 | a0001c0001t0001g0075a0001c0001t0002g0322a0001c0001t0007g0003others(15): Show | 20 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.-282+7531dupA | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404275 | ||||||
chr11:134404290
|
G | A | 8 | a0001c0001t0001g0217a0001c0001t0001g0236a0001c0001t0003g0222others(5): Show | 8 | HG02257.hp2 HG02809.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.-282+7517C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404290 | ||||||
chr11:134404445
|
A | T | 1 | a0001c0001t0013g0318 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-282+7362T>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404445 | ||||||
chr11:134404484
|
C | T | 2 | a0001c0001t0009g0240a0001c0001t0026g0015 | 2 | NA18964.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-282+7323G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404484 | ||||||
chr11:134404656
|
C | A | 17 | a0001c0001t0001g0075a0001c0001t0002g0322a0001c0001t0007g0003others(14): Show | 19 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.-282+7151G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404656 | ||||||
chr11:134404681
|
G | A | 28 | a0001c0001t0001g0075a0001c0001t0002g0322a0001c0001t0004g0248others(25): Show | 30 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.-282+7126C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404681 | ||||||
chr11:134404694
|
C | T | 3 | a0001c0001t0001g0193a0001c0001t0003g0191a0001c0001t0003g0192 | 3 | HG01884.hp1 HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-282+7113G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404694 | ||||||
chr11:134404782
|
A | G | 82 | a0001c0001t0001g0063a0001c0001t0001g0075a0001c0001t0001g0097others(79): Show | 87 | HG00544.hp1 HG00673.hp2 HG01069.hp1 others(84): Show |
intron_variant | MODIFIER | c.-282+7025T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404782 | ||||||
chr11:134404816
|
A | G | 81 | a0001c0001t0001g0063a0001c0001t0001g0075a0001c0001t0001g0097others(78): Show | 86 | HG00544.hp1 HG00673.hp2 HG01069.hp1 others(83): Show |
intron_variant | MODIFIER | c.-282+6991T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404816 | ||||||
chr11:134404820
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-282+6987C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404820 | ||||||
chr11:134404831
|
A | G | 2 | a0001c0001t0001g0086a0001c0001t0003g0085 | 2 | HG00639.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.-282+6976T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404831 | ||||||
chr11:134404869
|
C | T | 34 | a0001c0001t0001g0063a0001c0001t0001g0193a0001c0001t0001g0224others(31): Show | 35 | HG01074.hp2 HG01243.hp1 HG01256.hp1 others(32): Show |
intron_variant | MODIFIER | c.-282+6938G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404869 | ||||||
chr11:134404885
|
C | G | 1 | a0001c0001t0003g0070 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-282+6922G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404885 | ||||||
chr11:134404979
|
T | C | 1 | a0001c0001t0008g0161 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-282+6828A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404979 | ||||||
chr11:134405066
|
G | C | 1 | a0001c0001t0004g0269 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-282+6741C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134405066 | ||||||
chr11:134405095
|
T | TG | 10 | a0001c0001t0001g0236a0001c0001t0004g0261a0001c0001t0006g0039others(7): Show | 10 | HG00544.hp2 HG02602.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.-282+6711dupC | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134405095 | ||||||
chr11:134405101
|
G | A | 1 | a0001c0001t0050g0272 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-282+6706C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134405101 | ||||||
chr11:134405129
|
G | A | 2 | a0001c0001t0031g0026a0001c0001t0054g0285 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-282+6678C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134405129 | ||||||
chr11:134405559
|
C | T | 30 | a0001c0001t0001g0193a0001c0001t0001g0224a0001c0001t0002g0323others(27): Show | 32 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.-282+6248G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134405559 | ||||||
chr11:134405561
|
G | A | 1 | a0001c0001t0003g0179 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-282+6246C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134405561 | ||||||
chr11:134405643
|
C | A | 19 | a0001c0001t0001g0193a0001c0001t0001g0224a0001c0001t0003g0191others(16): Show | 19 | HG01074.hp2 HG01243.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.-282+6164G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134405643 | ||||||
chr11:134405675
|
C | T | 7 | a0001c0001t0001g0005a0001c0001t0001g0071a0001c0001t0001g0072others(4): Show | 8 | NA18948.hp1 NA18951.hp1 NA18963.hp2 others(5): Show |
intron_variant | MODIFIER | c.-282+6132G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134405675 | ||||||
chr11:134405742
|
AG | A | 14 | a0001c0001t0001g0063a0001c0001t0004g0011a0001c0001t0004g0253others(11): Show | 15 | HG01256.hp1 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.-282+6064delC | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134405742 | ||||||
chr11:134405788
|
T | A | 1 | a0001c0001t0009g0243 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-282+6019A>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134405788 | ||||||
chr11:134405850
|
C | T | 1 | a0003c0004t0001g0164 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-282+5957G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134405850 | ||||||
chr11:134405852
|
A | G | 334 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(331): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.-282+5955T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134405852 | ||||||
chr11:134405962
|
C | T | 1 | a0001c0001t0007g0089 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-282+5845G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134405962 | ||||||
chr11:134406028
|
C | T | 26 | a0001c0001t0001g0075a0001c0001t0001g0088a0001c0001t0002g0322others(23): Show | 28 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.-282+5779G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134406028 | ||||||
chr11:134406092
|
G | A | 51 | a0001c0001t0001g0063a0001c0001t0001g0075a0001c0001t0002g0322others(48): Show | 56 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(53): Show |
intron_variant | MODIFIER | c.-282+5715C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134406092 | ||||||
chr11:134406167
|
C | T | 2 | a0001c0001t0008g0196a0001c0001t0008g0197 | 2 | HG01433.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-282+5640G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134406167 | ||||||
chr11:134406248
|
A | G | 76 | a0001c0001t0001g0063a0001c0001t0001g0075a0001c0001t0001g0193others(73): Show | 81 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(78): Show |
intron_variant | MODIFIER | c.-282+5559T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134406248 | ||||||
chr11:134406408
|
A | G | 50 | a0001c0001t0001g0063a0001c0001t0001g0075a0001c0001t0002g0322others(47): Show | 53 | HG01069.hp1 HG01071.hp1 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.-282+5399T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134406408 | ||||||
chr11:134406472
|
C | A | 1 | a0001c0001t0001g0162 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-282+5335G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134406472 | ||||||
chr11:134406938
|
A | AGGTCCAC others(51): Show |
52 | a0001c0001t0001g0063a0001c0001t0001g0193a0001c0001t0001g0224others(49): Show | 55 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.-282+4868_-282+486 others(62): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134406938 | ||||||
chr11:134406970
|
C | A | 9 | a0001c0001t0009g0240a0001c0001t0009g0241a0001c0001t0009g0242others(6): Show | 9 | HG02015.hp2 HG02056.hp2 HG03688.hp2 others(6): Show |
intron_variant | MODIFIER | c.-282+4837G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134406970 | ||||||
chr11:134406971
|
G | A | 1 | a0001c0001t0047g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-282+4836C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134406971 | ||||||
chr11:134407076
|
C | T | 29 | a0001c0001t0001g0063a0001c0001t0002g0323a0001c0001t0002g0324others(26): Show | 30 | HG01081.hp2 HG01256.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.-282+4731G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134407076 | ||||||
chr11:134407316
|
T | C | 3 | a0001c0001t0001g0078a0001c0001t0001g0163a0001c0001t0006g0041 | 3 | HG00408.hp2 NA18942.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.-282+4491A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134407316 | ||||||
chr11:134407558
|
C | T | 5 | a0001c0001t0004g0001a0001c0001t0004g0260a0001c0001t0004g0261others(2): Show | 7 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-282+4249G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134407558 | ||||||
chr11:134407603
|
A | C | 1 | a0001c0001t0001g0071 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-282+4204T>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134407603 | ||||||
chr11:134407635
|
C | T | 1 | a0001c0001t0005g0289 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-282+4172G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134407635 | ||||||
chr11:134407736
|
C | CA | 32 | a0001c0001t0001g0193a0001c0001t0001g0224a0001c0001t0003g0165others(29): Show | 32 | HG00438.hp1 HG01074.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.-282+4070dupT | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134407736 | ||||||
chr11:134407736
|
C | CAA | 5 | a0001c0001t0004g0001a0001c0001t0004g0260a0001c0001t0004g0261others(2): Show | 7 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-282+4069_-282+407 others(6): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134407736 | ||||||
chr11:134407766
|
T | G | 5 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(2): Show | 5 | HG00609.hp1 NA18960.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.-282+4041A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134407766 | ||||||
chr11:134407856
|
G | A | 29 | a0001c0001t0001g0063a0001c0001t0002g0323a0001c0001t0002g0324others(26): Show | 30 | HG01081.hp2 HG01256.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.-282+3951C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134407856 | ||||||
chr11:134407921
|
C | T | 6 | a0001c0001t0002g0323a0001c0001t0002g0324a0001c0001t0002g0325others(3): Show | 6 | HG01081.hp2 HG01891.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-282+3886G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134407921 | ||||||
chr11:134407972
|
A | AT | 52 | a0001c0001t0001g0063a0001c0001t0001g0193a0001c0001t0001g0224others(49): Show | 55 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.-282+3834dupA | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134407972 | ||||||
chr11:134407987
|
C | T | 1 | a0001c0001t0001g0087 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-282+3820G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134407987 | ||||||
chr11:134407990
|
C | A | 1 | a0001c0001t0001g0213 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-282+3817G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134407990 | ||||||
chr11:134408084
|
G | A | 69 | a0001c0001t0001g0063a0001c0001t0001g0193a0001c0001t0001g0224others(66): Show | 72 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(69): Show |
intron_variant | MODIFIER | c.-282+3723C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408084 | ||||||
chr11:134408116
|
G | T | 29 | a0001c0001t0001g0063a0001c0001t0002g0323a0001c0001t0002g0324others(26): Show | 30 | HG01081.hp2 HG01256.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.-282+3691C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408116 | ||||||
chr11:134408157
|
C | CGGGTGAG others(75): Show |
9 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172others(6): Show | 9 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.-282+3649_-282+365 others(86): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408157 | ||||||
chr11:134408157
|
C | CGGGTGAG others(75): Show |
263 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(260): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.-282+3649_-282+365 others(86): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408157 | ||||||
chr11:134408157
|
C | CGGGTGAG others(608): Show |
2 | a0001c0001t0001g0086a0001c0001t0003g0085 | 2 | HG00639.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.-282+3649_-282+365 others(619): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408157 | ||||||
chr11:134408188
|
C | CGATTCCA others(75): Show |
4 | a0001c0001t0003g0081a0001c0001t0003g0083a0001c0001t0003g0084others(1): Show | 4 | HG01192.hp2 HG02723.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-282+3618_-282+361 others(86): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408188 | ||||||
chr11:134408225
|
G | C | 9 | a0001c0001t0004g0248a0001c0001t0004g0252a0001c0001t0004g0269others(6): Show | 9 | HG02280.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-282+3582C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408225 | ||||||
chr11:134408225
|
G | GCACCGAC others(116): Show |
12 | a0001c0001t0003g0195a0001c0001t0010g0189a0001c0001t0045g0223others(9): Show | 12 | HG01074.hp2 HG02258.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-282+3581_-282+358 others(127): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408225 | ||||||
chr11:134408225
|
G | GCACCGAC others(1428): Show |
1 | a0001c0001t0001g0193 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-282+3581_-282+358 others(1439): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408225 | ||||||
chr11:134408225
|
G | GCACCGAC others(4134): Show |
1 | a0001c0001t0001g0224 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-282+3581_-282+358 others(4145): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408225 | ||||||
chr11:134408225
|
G | GCACCGAC others(1469): Show |
2 | a0001c0001t0003g0191a0001c0001t0003g0192 | 2 | HG01884.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.-282+3581_-282+358 others(1480): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408225 | ||||||
chr11:134408225
|
G | GCACCGAC others(1428): Show |
1 | a0002c0002t0001g0229 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-282+3581_-282+358 others(1439): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408225 | ||||||
chr11:134408230
|
T | G | 34 | a0001c0001t0001g0178a0001c0001t0003g0195a0001c0001t0004g0001others(31): Show | 36 | HG01074.hp2 HG01168.hp2 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.-282+3577A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408230 | ||||||
chr11:134408230
|
T | TATTCCAG others(198): Show |
1 | a0001c0001t0035g0030 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-282+3576_-282+357 others(209): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408230 | ||||||
chr11:134408232
|
T | C | 11 | a0001c0001t0001g0178a0001c0001t0004g0001a0001c0001t0004g0260others(8): Show | 13 | HG01168.hp2 HG01169.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.-282+3575A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408232 | ||||||
chr11:134408235
|
T | C | 60 | a0001c0001t0001g0063a0001c0001t0001g0178a0001c0001t0001g0193others(57): Show | 63 | HG01074.hp2 HG01081.hp2 HG01168.hp2 others(60): Show |
intron_variant | MODIFIER | c.-282+3572A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408235 | ||||||
chr11:134408237
|
G | A | 11 | a0001c0001t0001g0178a0001c0001t0004g0001a0001c0001t0004g0260others(8): Show | 13 | HG01168.hp2 HG01169.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.-282+3570C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408237 | ||||||
chr11:134408246
|
A | G | 59 | a0001c0001t0001g0063a0001c0001t0001g0178a0001c0001t0001g0193others(56): Show | 62 | HG01074.hp2 HG01081.hp2 HG01168.hp2 others(59): Show |
intron_variant | MODIFIER | c.-282+3561T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408246 | ||||||
chr11:134408266
|
G | GCACCGAC others(116): Show |
3 | a0001c0001t0018g0023a0001c0001t0022g0257a0001c0001t0022g0258 | 3 | HG01256.hp1 HG01934.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.-282+3540_-282+354 others(127): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408266 | ||||||
chr11:134408271
|
G | GATTCCAG others(116): Show |
1 | a0001c0001t0004g0269 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-282+3535_-282+353 others(127): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408271 | ||||||
chr11:134408271
|
G | T | 12 | a0001c0001t0003g0195a0001c0001t0010g0189a0001c0001t0045g0223others(9): Show | 12 | HG01074.hp2 HG02258.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-282+3536C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408271 | ||||||
chr11:134408273
|
T | C | 16 | a0001c0001t0001g0063a0001c0001t0002g0323a0001c0001t0002g0324others(13): Show | 17 | HG01081.hp2 HG01257.hp1 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-282+3534A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408273 | ||||||
chr11:134408278
|
G | C | 3 | a0001c0001t0013g0317a0001c0001t0013g0318a0001c0001t0013g0332 | 3 | HG01496.hp2 HG02572.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-282+3529C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408278 | ||||||
chr11:134408281
|
G | C | 3 | a0001c0001t0018g0023a0001c0001t0022g0257a0001c0001t0022g0258 | 3 | HG01256.hp1 HG01934.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.-282+3526C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408281 | ||||||
chr11:134408287
|
G | GGAGGGAG others(34): Show |
4 | a0001c0001t0001g0178a0001c0001t0005g0279a0001c0001t0031g0026others(1): Show | 4 | HG01168.hp2 HG01169.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.-282+3519_-282+352 others(45): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408287 | ||||||
chr11:134408312
|
G | GATTCCAG others(280): Show |
1 | a0001c0003t0001g0235 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-282+3208_-282+349 others(291): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408312 | ||||||
chr11:134408312
|
G | T | 2 | a0001c0001t0005g0319a0001c0001t0024g0288 | 2 | HG02683.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-282+3495C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408312 | ||||||
chr11:134408314
|
T | C | 16 | a0001c0001t0001g0063a0001c0001t0002g0323a0001c0001t0002g0324others(13): Show | 17 | HG01081.hp2 HG01257.hp1 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-282+3493A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408314 | ||||||
chr11:134408317
|
C | T | 2 | a0001c0001t0005g0319a0001c0001t0024g0288 | 2 | HG02683.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-282+3490G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408317 | ||||||
chr11:134408328
|
G | A | 2 | a0001c0001t0005g0319a0001c0001t0024g0288 | 2 | HG02683.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-282+3479C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408328 | ||||||
chr11:134408333
|
G | C | 1 | a0001c0001t0004g0252 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-282+3474C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408333 | ||||||
chr11:134408348
|
G | C | 16 | a0001c0001t0001g0063a0001c0001t0002g0323a0001c0001t0002g0324others(13): Show | 17 | HG01081.hp2 HG01257.hp1 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-282+3459C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408348 | ||||||
chr11:134408353
|
G | T | 13 | a0001c0001t0003g0195a0001c0001t0010g0189a0001c0001t0035g0030others(10): Show | 13 | HG01074.hp2 HG02258.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-282+3454C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408353 | ||||||
chr11:134408389
|
C | CCACCTAT others(75): Show |
1 | a0001c0001t0044g0057 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-282+3417_-282+341 others(86): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408389 | ||||||
chr11:134408389
|
C | CCACCTAT others(321): Show |
4 | a0001c0001t0004g0248a0001c0003t0004g0249a0001c0003t0004g0250others(1): Show | 4 | HG02572.hp1 HG02717.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-282+3417_-282+341 others(332): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408389 | ||||||
chr11:134408389
|
C | G | 35 | a0001c0001t0001g0178a0001c0001t0001g0193a0001c0001t0001g0224others(32): Show | 37 | HG01074.hp2 HG01243.hp1 HG01256.hp1 others(34): Show |
intron_variant | MODIFIER | c.-282+3418G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408389 | ||||||
chr11:134408393
|
C | CTATTCCA others(198): Show |
1 | a0002c0002t0002g0334 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-282+3413_-282+341 others(209): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408393 | ||||||
chr11:134408394
|
G | GATTCCAG others(34): Show |
1 | a0001c0001t0044g0057 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-282+3412_-282+341 others(45): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408394 | ||||||
chr11:134408394
|
G | T | 10 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0239others(7): Show | 12 | HG02109.hp1 HG02451.hp2 HG02896.hp2 others(9): Show |
intron_variant | MODIFIER | c.-282+3413C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408394 | ||||||
chr11:134408396
|
T | C | 4 | a0001c0001t0003g0176a0001c0001t0003g0177a0001c0001t0025g0014others(1): Show | 4 | HG02698.hp1 HG02735.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-282+3411A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408396 | ||||||
chr11:134408396
|
T | TTCCAGTG others(239): Show |
10 | a0001c0001t0001g0063a0001c0001t0004g0011a0001c0001t0004g0253others(7): Show | 11 | HG01257.hp1 HG01258.hp2 HG03834.hp2 others(8): Show |
intron_variant | MODIFIER | c.-282+3410_-282+341 others(250): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408396 | ||||||
chr11:134408396
|
T | TTCCAGTG others(116): Show |
3 | a0001c0001t0018g0023a0001c0001t0022g0257a0001c0001t0022g0258 | 3 | HG01256.hp1 HG01934.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.-282+3410_-282+341 others(127): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408396 | ||||||
chr11:134408404
|
G | C | 1 | a0001c0001t0018g0024 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-282+3403C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408404 | ||||||
chr11:134408430
|
G | C | 2 | a0001c0001t0001g0178a0001c0001t0005g0279 | 2 | NA18964.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.-282+3377C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408430 | ||||||
chr11:134408430
|
G | GCACCTAT others(280): Show |
1 | a0001c0001t0004g0252 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-282+3376_-282+337 others(291): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408430 | ||||||
chr11:134408435
|
G | T | 1 | a0001c0001t0004g0248 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-282+3372C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408435 | ||||||
chr11:134408437
|
C | T | 28 | a0001c0001t0001g0178a0001c0001t0001g0193a0001c0001t0001g0224others(25): Show | 30 | HG01081.hp2 HG01243.hp1 HG01261.hp2 others(27): Show |
intron_variant | MODIFIER | c.-282+3370G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408437 | ||||||
chr11:134408471
|
G | C | 14 | a0001c0001t0001g0063a0001c0001t0004g0011a0001c0001t0004g0253others(11): Show | 15 | HG01256.hp1 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.-282+3336C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408471 | ||||||
chr11:134408471
|
G | GCACCGAT others(239): Show |
5 | a0001c0001t0002g0323a0001c0001t0002g0324a0001c0001t0002g0325others(2): Show | 5 | HG01081.hp2 HG01891.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-282+3335_-282+333 others(250): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408471 | ||||||
chr11:134408478
|
T | C | 15 | a0001c0001t0001g0178a0001c0001t0002g0322a0001c0001t0003g0195others(12): Show | 15 | HG01074.hp2 HG01243.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-282+3329A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408478 | ||||||
chr11:134408512
|
G | C | 2 | a0001c0001t0035g0030a0001c0001t0044g0057 | 2 | HG02897.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-282+3295C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408512 | ||||||
chr11:134408517
|
G | GACTCCAG others(321): Show |
2 | a0002c0002t0001g0227a0002c0002t0001g0228 | 2 | HG01243.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.-282+3289_-282+329 others(332): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408517 | ||||||
chr11:134408519
|
T | C | 14 | a0001c0001t0002g0322a0001c0001t0003g0195a0001c0001t0005g0319others(11): Show | 14 | HG01074.hp2 HG01243.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-282+3288A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408519 | ||||||
chr11:134408547
|
T | C | 57 | a0001c0001t0001g0063a0001c0001t0001g0178a0001c0001t0001g0193others(54): Show | 60 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(57): Show |
intron_variant | MODIFIER | c.-282+3260A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408547 | ||||||
chr11:134408553
|
G | GCACCGAT others(75): Show |
6 | a0001c0001t0001g0063a0001c0001t0004g0011a0001c0001t0004g0254others(3): Show | 6 | HG01256.hp1 HG01258.hp2 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.-282+3253_-282+325 others(86): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408553 | ||||||
chr11:134408558
|
T | G | 40 | a0001c0001t0001g0063a0001c0001t0001g0178a0001c0001t0002g0322others(37): Show | 41 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.-282+3249A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408558 | ||||||
chr11:134408558
|
T | TATTCCAG others(34): Show |
6 | a0001c0001t0004g0248a0001c0001t0004g0252a0001c0003t0004g0249others(3): Show | 6 | HG02280.hp1 HG02451.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-282+3248_-282+324 others(45): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408558 | ||||||
chr11:134408558
|
T | TATTCCAG others(157): Show |
1 | a0001c0001t0018g0024 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-282+3248_-282+324 others(168): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408558 | ||||||
chr11:134408560
|
T | C | 3 | a0001c0001t0044g0057a0002c0002t0001g0227a0002c0002t0001g0228 | 3 | HG01243.hp1 HG02055.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-282+3247A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408560 | ||||||
chr11:134408588
|
C | T | 2 | a0001c0001t0001g0178a0001c0001t0005g0279 | 2 | NA18964.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.-282+3219G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408588 | ||||||
chr11:134408599
|
T | G | 35 | a0001c0001t0001g0063a0001c0001t0001g0224a0001c0001t0002g0323others(32): Show | 38 | HG01081.hp2 HG01256.hp1 HG01257.hp1 others(35): Show |
intron_variant | MODIFIER | c.-282+3208A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408599 | ||||||
chr11:134408601
|
T | TTCCAGTG others(34): Show |
5 | a0001c0001t0002g0323a0001c0001t0002g0324a0001c0001t0002g0325others(2): Show | 5 | HG01081.hp2 HG01891.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-282+3205_-282+320 others(45): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408601 | ||||||
chr11:134408609
|
G | GGGTGAGG others(116): Show |
1 | a0001c0001t0004g0269 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-282+3197_-282+319 others(127): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408609 | ||||||
chr11:134408616
|
G | C | 1 | a0001c0001t0003g0060 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-282+3191C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408616 | ||||||
chr11:134408629
|
C | T | 1 | a0001c0001t0005g0319 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-282+3178G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408629 | ||||||
chr11:134408632
|
C | T | 1 | a0001c0001t0018g0024 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-282+3175G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408632 | ||||||
chr11:134408635
|
G | C | 8 | a0001c0001t0004g0011a0001c0001t0004g0253a0001c0001t0004g0255others(5): Show | 8 | HG01257.hp1 HG01934.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.-282+3172C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408635 | ||||||
chr11:134408635
|
G | GCACCGTC others(444): Show |
1 | a0001c0001t0047g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-282+3171_-282+317 others(455): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408635 | ||||||
chr11:134408640
|
G | GATTCCAG others(75): Show |
1 | a0001c0001t0035g0030 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-282+3166_-282+316 others(86): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408640 | ||||||
chr11:134408640
|
G | GATTCCAG others(198): Show |
1 | a0001c0001t0055g0287 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-282+3166_-282+316 others(209): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408640 | ||||||
chr11:134408640
|
G | T | 8 | a0001c0001t0001g0178a0001c0001t0004g0001a0001c0001t0004g0260others(5): Show | 10 | HG02109.hp1 HG02683.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.-282+3167C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408640 | ||||||
chr11:134408642
|
T | C | 6 | a0001c0001t0001g0063a0001c0001t0004g0011a0001c0001t0004g0254others(3): Show | 6 | HG01256.hp1 HG01258.hp2 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.-282+3165A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408642 | ||||||
chr11:134408642
|
T | TTCCAGTG others(526): Show |
7 | a0002c0002t0001g0219a0002c0002t0001g0225a0002c0002t0001g0226others(4): Show | 7 | HG01074.hp2 HG02258.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-282+3164_-282+316 others(537): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408642 | ||||||
chr11:134408642
|
T | TTCCAGTG others(526): Show |
1 | a0001c0001t0010g0189 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-282+3164_-282+316 others(537): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408642 | ||||||
chr11:134408665
|
T | C | 2 | a0002c0002t0001g0227a0002c0002t0001g0228 | 2 | HG01243.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.-282+3142A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408665 | ||||||
chr11:134408670
|
T | C | 48 | a0001c0001t0001g0063a0001c0001t0001g0178a0001c0001t0001g0193others(45): Show | 51 | HG01081.hp2 HG01256.hp1 HG01257.hp1 others(48): Show |
intron_variant | MODIFIER | c.-282+3137A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408670 | ||||||
chr11:134408676
|
G | C | 10 | a0001c0001t0010g0189a0002c0002t0001g0219a0002c0002t0001g0225others(7): Show | 10 | HG01074.hp2 HG01243.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.-282+3131C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408676 | ||||||
chr11:134408676
|
G | GCACCGAT others(526): Show |
1 | a0001c0001t0045g0223 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-282+3130_-282+313 others(537): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408676 | ||||||
chr11:134408681
|
T | G | 38 | a0001c0001t0001g0193a0001c0001t0001g0224a0001c0001t0002g0323others(35): Show | 40 | HG01081.hp2 HG01257.hp1 HG01261.hp2 others(37): Show |
intron_variant | MODIFIER | c.-282+3126A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408681 | ||||||
chr11:134408706
|
T | C | 1 | a0001c0001t0045g0223 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-282+3101A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408706 | ||||||
chr11:134408711
|
C | T | 1 | a0001c0001t0005g0279 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-282+3096G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408711 | ||||||
chr11:134408717
|
G | C | 1 | a0001c0001t0018g0024 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-282+3090C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408717 | ||||||
chr11:134408717
|
G | GCACCGAC others(116): Show |
7 | a0001c0001t0004g0011a0001c0001t0004g0253a0001c0001t0004g0255others(4): Show | 7 | HG01257.hp1 HG01934.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.-282+3089_-282+309 others(127): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408717 | ||||||
chr11:134408717
|
G | GCACCGAT others(34): Show |
6 | a0001c0001t0001g0063a0001c0001t0004g0011a0001c0001t0004g0254others(3): Show | 6 | HG01256.hp1 HG01258.hp2 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.-282+3089_-282+309 others(45): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408717 | ||||||
chr11:134408722
|
G | GATTCCAG others(198): Show |
1 | a0001c0001t0001g0187 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-282+3084_-282+308 others(209): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408722 | ||||||
chr11:134408722
|
G | GATTCCAG others(198): Show |
1 | a0001c0001t0001g0080 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-282+2880_-282+308 others(209): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408722 | ||||||
chr11:134408722
|
G | T | 1 | a0001c0001t0005g0279 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-282+3085C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408722 | ||||||
chr11:134408724
|
T | C | 7 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0183others(4): Show | 7 | HG01433.hp2 HG01515.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.-282+3083A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408724 | ||||||
chr11:134408724
|
T | TTCCAGTG others(321): Show |
1 | a0001c0001t0004g0252 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-282+3082_-282+308 others(332): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408724 | ||||||
chr11:134408758
|
G | GCACCGAT others(1100): Show |
2 | a0002c0002t0001g0227a0002c0002t0001g0228 | 2 | HG01243.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.-282+3048_-282+304 others(1111): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408758 | ||||||
chr11:134408763
|
T | G | 36 | a0001c0001t0001g0063a0001c0001t0001g0187a0001c0001t0001g0193others(33): Show | 37 | HG01081.hp2 HG01256.hp1 HG01257.hp1 others(34): Show |
intron_variant | MODIFIER | c.-282+3044A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408763 | ||||||
chr11:134408763
|
T | TATTCCAG others(34): Show |
1 | a0001c0001t0044g0057 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-282+3003_-282+304 others(45): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408763 | ||||||
chr11:134408763
|
T | TATTCCAG others(485): Show |
2 | a0001c0001t0004g0001a0001c0001t0014g0054 | 2 | HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-282+3043_-282+304 others(496): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408763 | ||||||
chr11:134408804
|
G | GATTCCAG others(362): Show |
1 | a0001c0001t0004g0259 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-282+3002_-282+300 others(373): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408804 | ||||||
chr11:134408804
|
G | GATTCCAG others(608): Show |
4 | a0001c0001t0004g0001a0001c0001t0004g0260a0001c0001t0004g0261others(1): Show | 5 | HG02109.hp1 HG02897.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-282+3002_-282+300 others(619): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408804 | ||||||
chr11:134408804
|
G | T | 1 | a0001c0001t0005g0279 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-282+3003C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408804 | ||||||
chr11:134408806
|
C | CTCCAGTG others(157): Show |
1 | a0001c0001t0001g0079 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-282+2837_-282+300 others(168): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408806 | ||||||
chr11:134408806
|
C | T | 21 | a0001c0001t0001g0193a0001c0001t0001g0224a0001c0001t0003g0191others(18): Show | 22 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.-282+3001G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408806 | ||||||
chr11:134408834
|
C | T | 1 | a0001c0001t0004g0252 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-282+2973G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408834 | ||||||
chr11:134408837
|
C | T | 1 | a0001c0001t0007g0231 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-282+2970G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408837 | ||||||
chr11:134408845
|
T | G | 19 | a0001c0001t0001g0193a0001c0001t0001g0224a0001c0001t0003g0191others(16): Show | 19 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-282+2962A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408845 | ||||||
chr11:134408845
|
T | TATTCCAG others(34): Show |
1 | a0001c0001t0018g0024 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-282+2921_-282+296 others(45): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408845 | ||||||
chr11:134408847
|
T | C | 3 | a0001c0001t0004g0252a0002c0002t0001g0227a0002c0002t0001g0228 | 3 | HG01243.hp1 HG02055.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-282+2960A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408847 | ||||||
chr11:134408886
|
G | T | 3 | a0001c0001t0001g0217a0002c0002t0001g0227a0002c0002t0001g0228 | 3 | HG01243.hp1 HG02055.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-282+2921C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408886 | ||||||
chr11:134408911
|
T | C | 11 | a0001c0001t0004g0001a0001c0001t0010g0189a0001c0001t0014g0054others(8): Show | 11 | HG01074.hp2 HG02258.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-282+2896A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408911 | ||||||
chr11:134408916
|
T | C | 24 | a0001c0001t0001g0193a0001c0001t0001g0224a0001c0001t0003g0191others(21): Show | 25 | HG01243.hp1 HG01261.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.-282+2891A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408916 | ||||||
chr11:134408922
|
C | G | 25 | a0001c0001t0001g0078a0001c0001t0001g0193a0001c0001t0001g0224others(22): Show | 26 | HG00408.hp2 HG01243.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.-282+2885G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408922 | ||||||
chr11:134408927
|
T | G | 23 | a0001c0001t0001g0193a0001c0001t0001g0224a0001c0001t0003g0191others(20): Show | 24 | HG01243.hp1 HG01261.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.-282+2880A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408927 | ||||||
chr11:134408927
|
T | TATTCCAG others(116): Show |
19 | a0001c0001t0001g0063a0001c0001t0002g0323a0001c0001t0002g0324others(16): Show | 20 | HG01081.hp2 HG01256.hp1 HG01257.hp1 others(17): Show |
intron_variant | MODIFIER | c.-282+2879_-282+288 others(127): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408927 | ||||||
chr11:134408927
|
T | TATTCCAG others(116): Show |
1 | a0001c0001t0014g0053 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-282+2879_-282+288 others(127): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408927 | ||||||
chr11:134408929
|
T | C | 2 | a0002c0002t0001g0227a0002c0002t0001g0228 | 2 | HG01243.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.-282+2878A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408929 | ||||||
chr11:134408929
|
T | TTCCAGTG others(1633): Show |
1 | a0002c0002t0001g0190 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-282+2877_-282+287 others(1644): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408929 | ||||||
chr11:134408929
|
T | TTCCAGTG others(1838): Show |
2 | a0001c0001t0003g0195a0002c0002t0001g0194 | 2 | HG02615.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-282+2877_-282+287 others(1849): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408929 | ||||||
chr11:134408929
|
T | TTCCAGTG others(526): Show |
5 | a0001c0001t0001g0193a0001c0001t0001g0224a0001c0001t0003g0191others(2): Show | 5 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.-282+2877_-282+287 others(537): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408929 | ||||||
chr11:134408929
|
T | TTCCAGTG others(1346): Show |
1 | a0002c0002t0001g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-282+2877_-282+287 others(1357): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408929 | ||||||
chr11:134408929
|
T | TTCCAGTG others(1305): Show |
1 | a0001c0001t0010g0189 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-282+2877_-282+287 others(1316): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408929 | ||||||
chr11:134408929
|
T | TTCCAGTG others(1346): Show |
6 | a0002c0002t0001g0225a0002c0002t0001g0226a0002c0002t0001g0234others(3): Show | 6 | HG01074.hp2 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-282+2877_-282+287 others(1357): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408929 | ||||||
chr11:134408929
|
T | TTCCAGTG others(1305): Show |
1 | a0001c0001t0045g0223 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-282+2877_-282+287 others(1316): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408929 | ||||||
chr11:134409226
|
C | G | 2 | a0001c0001t0001g0077a0001c0001t0003g0076 | 2 | NA18982.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.-282+2581G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134409226 | ||||||
chr11:134409233
|
G | C | 3 | a0001c0001t0001g0184a0001c0001t0007g0009a0001c0001t0007g0185 | 4 | HG01070.hp2 HG01071.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.-282+2574C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134409233 | ||||||
chr11:134409234
|
C | T | 1 | a0001c0001t0002g0286 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-282+2573G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134409234 | ||||||
chr11:134409268
|
C | T | 6 | a0001c0001t0001g0075a0001c0001t0007g0003a0001c0001t0010g0004others(3): Show | 8 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.-282+2539G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134409268 | ||||||
chr11:134409297
|
A | G | 11 | a0001c0001t0001g0074a0001c0001t0002g0281a0001c0001t0002g0282others(8): Show | 11 | HG00558.hp1 HG02040.hp1 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.-282+2510T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134409297 | ||||||
chr11:134409458
|
T | C | 52 | a0001c0001t0001g0063a0001c0001t0001g0193a0001c0001t0001g0224others(49): Show | 55 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.-282+2349A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134409458 | ||||||
chr11:134409547
|
G | A | 2 | a0001c0001t0003g0186a0001c0001t0049g0271 | 2 | HG00099.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-282+2260C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134409547 | ||||||
chr11:134409595
|
C | A | 1 | a0001c0001t0046g0245 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-282+2212G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134409595 | ||||||
chr11:134409633
|
C | T | 5 | a0001c0001t0004g0264a0001c0001t0012g0263a0001c0001t0012g0265others(2): Show | 5 | HG02723.hp2 HG02976.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-282+2174G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134409633 | ||||||
chr11:134409697
|
C | A | 1 | a0001c0001t0001g0187 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-282+2110G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134409697 | ||||||
chr11:134409697
|
C | T | 19 | a0001c0001t0001g0193a0001c0001t0001g0224a0001c0001t0003g0191others(16): Show | 19 | HG01074.hp2 HG01243.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.-282+2110G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134409697 | ||||||
chr11:134409815
|
G | T | 1 | a0001c0001t0001g0073 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-282+1992C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134409815 | ||||||
chr11:134409830
|
G | A | 1 | a0001c0003t0048g0268 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-282+1977C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134409830 | ||||||
chr11:134409932
|
G | C | 1 | a0001c0001t0047g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-282+1875C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134409932 | ||||||
chr11:134409935
|
C | T | 1 | a0001c0001t0047g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-282+1872G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134409935 | ||||||
chr11:134409988
|
T | C | 48 | a0001c0001t0001g0063a0001c0001t0001g0193a0001c0001t0001g0224others(45): Show | 49 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.-282+1819A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134409988 | ||||||
chr11:134410036
|
A | C | 1 | a0001c0001t0001g0073 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-282+1771T>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410036 | ||||||
chr11:134410094
|
C | T | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | NA18966.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.-282+1713G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410094 | ||||||
chr11:134410156
|
C | T | 1 | a0001c0001t0004g0248 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-282+1651G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410156 | ||||||
chr11:134410170
|
G | A | 1 | a0001c0001t0002g0337 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-282+1637C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410170 | ||||||
chr11:134410173
|
G | A | 48 | a0001c0001t0001g0063a0001c0001t0001g0193a0001c0001t0001g0224others(45): Show | 49 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.-282+1634C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410173 | ||||||
chr11:134410176
|
G | T | 5 | a0001c0001t0004g0001a0001c0001t0004g0260a0001c0001t0004g0261others(2): Show | 7 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-282+1631C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410176 | ||||||
chr11:134410191
|
A | C | 1 | a0001c0001t0004g0252 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-282+1616T>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410191 | ||||||
chr11:134410232
|
A | C | 48 | a0001c0001t0001g0063a0001c0001t0001g0193a0001c0001t0001g0224others(45): Show | 49 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.-282+1575T>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410232 | ||||||
chr11:134410397
|
C | T | 5 | a0001c0001t0001g0198a0001c0001t0003g0070a0001c0001t0008g0196others(2): Show | 5 | HG01109.hp1 HG01433.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.-282+1410G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410397 | ||||||
chr11:134410549
|
T | C | 1 | a0001c0001t0004g0269 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-282+1258A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410549 | ||||||
chr11:134410609
|
G | T | 48 | a0001c0001t0001g0063a0001c0001t0001g0193a0001c0001t0001g0224others(45): Show | 49 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.-282+1198C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410609 | ||||||
chr11:134410610
|
C | T | 48 | a0001c0001t0001g0063a0001c0001t0001g0193a0001c0001t0001g0224others(45): Show | 49 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.-282+1197G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410610 | ||||||
chr11:134410627
|
T | C | 48 | a0001c0001t0001g0063a0001c0001t0001g0193a0001c0001t0001g0224others(45): Show | 49 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.-282+1180A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410627 | ||||||
chr11:134410630
|
C | T | 1 | a0002c0002t0002g0334 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-282+1177G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410630 | ||||||
chr11:134410666
|
G | A | 1 | a0001c0001t0045g0223 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-282+1141C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410666 | ||||||
chr11:134410668
|
C | G | 1 | a0001c0001t0015g0273 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-282+1139G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410668 | ||||||
chr11:134410728
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-282+1079G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410728 | ||||||
chr11:134410840
|
G | A | 1 | a0001c0001t0010g0189 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-282+967C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410840 | ||||||
chr11:134410843
|
C | T | 1 | a0001c0001t0020g0069 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-282+964G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410843 | ||||||
chr11:134410872
|
A | G | 64 | a0001c0001t0001g0063a0001c0001t0001g0193a0001c0001t0001g0224others(61): Show | 67 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(64): Show |
intron_variant | MODIFIER | c.-282+935T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410872 | ||||||
chr11:134410966
|
C | A | 59 | a0001c0001t0001g0063a0001c0001t0001g0193a0001c0001t0001g0224others(56): Show | 60 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(57): Show |
intron_variant | MODIFIER | c.-282+841G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410966 | ||||||
chr11:134411011
|
G | A | 1 | a0001c0001t0001g0188 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-282+796C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411011 | ||||||
chr11:134411031
|
G | C | 1 | a0001c0001t0047g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-282+776C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411031 | ||||||
chr11:134411084
|
G | A | 5 | a0001c0001t0004g0001a0001c0001t0004g0260a0001c0001t0004g0261others(2): Show | 7 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-282+723C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411084 | ||||||
chr11:134411108
|
A | C | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0006g0032 | 3 | HG00621.hp2 NA18984.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.-282+699T>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411108 | ||||||
chr11:134411137
|
T | C | 3 | a0001c0001t0002g0322a0001c0001t0003g0060a0001c0001t0053g0321 | 3 | HG01243.hp2 HG02257.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-282+670A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411137 | ||||||
chr11:134411249
|
C | A | 9 | a0001c0001t0001g0217a0001c0001t0001g0236a0001c0001t0003g0222others(6): Show | 9 | HG02257.hp2 HG02809.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.-282+558G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411249 | ||||||
chr11:134411309
|
C | T | 1 | a0001c0001t0010g0061 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-282+498G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411309 | ||||||
chr11:134411326
|
C | T | 36 | a0001c0001t0001g0193a0001c0001t0001g0224a0001c0001t0002g0323others(33): Show | 36 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.-282+481G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411326 | ||||||
chr11:134411344
|
C | T | 1 | a0001c0001t0003g0066 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-282+463G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411344 | ||||||
chr11:134411435
|
G | T | 11 | a0001c0001t0002g0323a0001c0001t0002g0324a0001c0001t0002g0325others(8): Show | 11 | HG01081.hp2 HG01891.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-282+372C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411435 | ||||||
chr11:134411438
|
T | G | 24 | a0001c0001t0001g0063a0001c0001t0004g0001a0001c0001t0004g0011others(21): Show | 27 | HG01256.hp1 HG01257.hp1 HG01258.hp2 others(24): Show |
intron_variant | MODIFIER | c.-282+369A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411438 | ||||||
chr11:134411601
|
C | G | 1 | a0001c0001t0045g0223 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-282+206G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411601 | ||||||
chr11:134411619
|
G | A | 1 | a0001c0001t0001g0218 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-282+188C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411619 | ||||||
chr11:134411663
|
G | T | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0034g0029 | 3 | NA18998.hp1 NA19054.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.-282+144C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411663 | ||||||
chr11:134411667
|
A | AGC | 5 | a0001c0001t0004g0001a0001c0001t0004g0260a0001c0001t0004g0261others(2): Show | 7 | HG02109.hp1 HG02809.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-282+138_-282+139d others(4): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411667 | ||||||
chr11:134411670
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G | GCA | 18 | a0001c0001t0001g0010a0001c0001t0002g0333a0001c0001t0002g0337others(15): Show | 19 | HG00738.hp2 HG01069.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.-282+135_-282+136d others(4): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411670 | ||||||
chr11:134411670
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G | GCACA | 16 | a0001c0001t0001g0224a0001c0001t0001g0230a0001c0001t0001g0237others(13): Show | 16 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.-282+133_-282+136d others(6): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411670 | ||||||
chr11:134411670
|
G | GCACACA | 3 | a0001c0003t0001g0235a0002c0002t0001g0234a0002c0002t0016g0018 | 3 | HG02258.hp1 HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-282+131_-282+136d others(8): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411670 | ||||||
chr11:134411670
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G | GCACACAC others(1): Show |
4 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0001g0239others(1): Show | 4 | HG02723.hp2 HG02922.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-282+129_-282+136d others(10): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411670 | ||||||
chr11:134411670
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GCA | G | 212 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(209): Show | 222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.-282+135_-282+136d others(4): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411670 | ||||||
chr11:134411670
|
GCACA | G | 15 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0004g0252others(12): Show | 15 | HG00642.hp2 HG01256.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.-282+133_-282+136d others(6): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411670 | ||||||
chr11:134411670
|
GCACACA | G | 7 | a0001c0001t0002g0277a0001c0001t0004g0248a0001c0001t0044g0057others(4): Show | 7 | HG01109.hp2 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-282+131_-282+136d others(8): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411670 | ||||||
chr11:134411670
|
GCACACAC others(3): Show |
G | 7 | a0001c0001t0009g0240a0001c0001t0009g0241a0001c0001t0009g0242others(4): Show | 7 | HG03688.hp2 NA18954.hp1 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.-282+127_-282+136d others(12): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411670 | ||||||
chr11:134411670
|
GCACACAC others(5): Show |
G | 1 | a0001c0001t0021g0056 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-282+125_-282+136d others(14): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411670 | ||||||
chr11:134411674
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A | G | 4 | a0001c0001t0003g0058a0001c0001t0003g0059a0001c0001t0003g0060others(1): Show | 4 | HG01255.hp1 HG02257.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-282+133T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411674 | ||||||
chr11:134411695
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C | G | 1 | a0001c0001t0047g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-282+112G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411695 | ||||||
chr11:134411765
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T | TG | 3 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0239 | 3 | HG02922.hp2 HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-282+41dupC | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411765 |