geneid | 10342 |
---|---|
ensemblid | ENSG00000114354.15 |
hgncid | 11758 |
symbol | TFG |
name | trafficking from ER to golgi regulator |
refseq_nuc | NM_006070.6 |
refseq_prot | NP_006061.2 |
ensembl_nuc | ENST00000240851.9 |
ensembl_prot | ENSP00000240851.4 |
mane_status | MANE Select |
chr | chr3 |
start | 100709494 |
end | 100748964 |
strand | + |
ver | v1.2 |
region | chr3:100709494-100748964 |
region5000 | chr3:100704494-100753964 |
regionname0 | TFG_chr3_100709494_100748964 |
regionname5000 | TFG_chr3_100704494_100753964 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1203 | 206 | 38 | 42 | 87 | 13 | 25 | TFG_chr3_100704494_100753964 | TFG | copy fasta | chr3 | 100704494 | 100753964 |
c0002 | 1/0 | 1203 | 123 | 31 | 21 | 61 | 2 | 7 | TFG_chr3_100704494_100753964 | TFG | copy fasta | chr3 | 100704494 | 100753964 |
c0003 | 0/0 | 1203 | 11 | 10 | 0 | 0 | 1 | 0 | TFG_chr3_100704494_100753964 | TFG | copy fasta | chr3 | 100704494 | 100753964 |
c0004 | 0/0 | 1203 | 9 | 8 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | copy fasta | chr3 | 100704494 | 100753964 |
c0005 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | copy fasta | chr3 | 100704494 | 100753964 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 705 | 124 | 29 | 21 | 58 | 7 | 8 | TFG_chr3_100704494_100753964 | TFG | copy fasta | chr3 | 100704494 | 100753964 |
t0002 | 1/0 | 705 | 119 | 30 | 18 | 61 | 2 | 7 | TFG_chr3_100704494_100753964 | TFG | copy fasta | chr3 | 100704494 | 100753964 |
t0003 | 0/0 | 705 | 77 | 22 | 13 | 25 | 6 | 11 | TFG_chr3_100704494_100753964 | TFG | copy fasta | chr3 | 100704494 | 100753964 |
t0004 | 0/0 | 705 | 10 | 0 | 2 | 2 | 1 | 5 | TFG_chr3_100704494_100753964 | TFG | copy fasta | chr3 | 100704494 | 100753964 |
t0005 | 0/0 | 703 | 6 | 0 | 5 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | copy fasta | chr3 | 100704494 | 100753964 |
t0006 | 0/0 | 706 | 4 | 3 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | copy fasta | chr3 | 100704494 | 100753964 |
t0007 | 0/0 | 705 | 3 | 0 | 3 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | copy fasta | chr3 | 100704494 | 100753964 |
t0008 | 0/0 | 705 | 2 | 2 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | copy fasta | chr3 | 100704494 | 100753964 |
t0009 | 0/0 | 705 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | copy fasta | chr3 | 100704494 | 100753964 |
t0010 | 0/0 | 705 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | copy fasta | chr3 | 100704494 | 100753964 |
t0011 | 0/0 | 705 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | copy fasta | chr3 | 100704494 | 100753964 |
t0012 | 0/0 | 705 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | copy fasta | chr3 | 100704494 | 100753964 |
t0013 | 0/0 | 705 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | copy fasta | chr3 | 100704494 | 100753964 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/1 | 33 | 5 | 3 | 20 | 4 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0002 | 0/0 | 18 | 0 | 0 | 18 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0003 | 0/0 | 14 | 2 | 9 | 1 | 2 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0004 | 0/0 | 11 | 0 | 1 | 7 | 1 | 2 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0005 | 0/0 | 7 | 0 | 1 | 5 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0008 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0009 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0010 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0014 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0015 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0016 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0018 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0021 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0028 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0036 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0165 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1203 | 206 | 38 | 42 | 87 | 13 | 25 | TFG_chr3_100704494_100753964 | TFG | copy fasta | chr3 | 100704494 | 100753964 |
a0001c0002 | 1/0 | 1203 | 123 | 31 | 21 | 61 | 2 | 7 | TFG_chr3_100704494_100753964 | TFG | copy fasta | chr3 | 100704494 | 100753964 |
a0001c0003 | 0/0 | 1203 | 11 | 10 | 0 | 0 | 1 | 0 | TFG_chr3_100704494_100753964 | TFG | copy fasta | chr3 | 100704494 | 100753964 |
a0001c0004 | 0/0 | 1203 | 9 | 8 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | copy fasta | chr3 | 100704494 | 100753964 |
a0002c0005 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | copy fasta | chr3 | 100704494 | 100753964 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 1907 | 104 | 11 | 20 | 58 | 6 | 8 | TFG_chr3_100704494_100753964 | TFG | copy fasta | chr3 | 100704494 | 100753964 |
a0001c0001t0003 | 0/0 | 1907 | 76 | 21 | 13 | 25 | 6 | 11 | TFG_chr3_100704494_100753964 | TFG | copy fasta | chr3 | 100704494 | 100753964 |
a0001c0001t0004 | 0/0 | 1907 | 10 | 0 | 2 | 2 | 1 | 5 | TFG_chr3_100704494_100753964 | TFG | copy fasta | chr3 | 100704494 | 100753964 |
a0001c0001t0005 | 0/0 | 1905 | 6 | 0 | 5 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | copy fasta | chr3 | 100704494 | 100753964 |
a0001c0001t0006 | 0/0 | 1908 | 4 | 3 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | copy fasta | chr3 | 100704494 | 100753964 |
a0001c0001t0008 | 0/0 | 1907 | 2 | 2 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | copy fasta | chr3 | 100704494 | 100753964 |
a0001c0001t0009 | 0/0 | 1907 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | copy fasta | chr3 | 100704494 | 100753964 |
a0001c0001t0010 | 0/0 | 1907 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | copy fasta | chr3 | 100704494 | 100753964 |
a0001c0001t0011 | 0/0 | 1907 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | copy fasta | chr3 | 100704494 | 100753964 |
a0001c0001t0012 | 0/0 | 1907 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | copy fasta | chr3 | 100704494 | 100753964 |
a0001c0002t0002 | 1/0 | 1907 | 119 | 30 | 18 | 61 | 2 | 7 | TFG_chr3_100704494_100753964 | TFG | copy fasta | chr3 | 100704494 | 100753964 |
a0001c0002t0007 | 0/0 | 1907 | 3 | 0 | 3 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | copy fasta | chr3 | 100704494 | 100753964 |
a0001c0002t0013 | 0/0 | 1907 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | copy fasta | chr3 | 100704494 | 100753964 |
a0001c0003t0001 | 0/0 | 1907 | 11 | 10 | 0 | 0 | 1 | 0 | TFG_chr3_100704494_100753964 | TFG | copy fasta | chr3 | 100704494 | 100753964 |
a0001c0004t0001 | 0/0 | 1907 | 9 | 8 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | copy fasta | chr3 | 100704494 | 100753964 |
a0002c0005t0003 | 0/0 | 1907 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | copy fasta | chr3 | 100704494 | 100753964 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/1 | 33 | 5 | 3 | 20 | 4 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0005 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0004 | 0/0 | 9 | 0 | 0 | 7 | 1 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0009 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0014 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0028 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0004g0008 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0004g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0005g0004 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0005g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0005g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0005g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0006g0015 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0008g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0008g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0009g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0010g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0011g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0001t0012g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0002 | 0/0 | 18 | 0 | 0 | 18 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0003 | 0/0 | 12 | 2 | 7 | 1 | 2 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0021 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0165 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0007g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0007g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0002t0013g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0003t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0003t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0003t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0003t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0003t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0003t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0003t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0003t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0004t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0004t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0004t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0004t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0004t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0001c0004t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
a0002c0005t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG00099 | hp2 | a0001 | c0001 | t0004 | g0075 | EUR | GBR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0004 | EUR | GBR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0120 | EUR | GBR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG00280 | hp1 | a0001 | c0003 | t0001 | g0044 | EUR | FIN | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0028 | EUR | FIN | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0056 | EUR | FIN | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0095 | EUR | FIN | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG00408 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | CHS | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG00438 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | CHS | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG00438 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | CHS | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG00544 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | CHS | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG00558 | hp2 | a0001 | c0002 | t0002 | g0042 | EAS | CHS | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG00597 | hp1 | a0001 | c0002 | t0002 | g0162 | EAS | CHS | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG00639 | hp1 | a0001 | c0002 | t0002 | g0173 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG00639 | hp2 | a0001 | c0002 | t0002 | g0163 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG00733 | hp2 | a0001 | c0002 | t0002 | g0021 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG00735 | hp1 | a0001 | c0004 | t0001 | g0207 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0080 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0032 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG00741 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01071 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0032 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01074 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01081 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01099 | hp1 | a0001 | c0002 | t0002 | g0179 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0087 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01109 | hp1 | a0001 | c0002 | t0002 | g0175 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01167 | hp1 | a0001 | c0001 | t0005 | g0004 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01167 | hp2 | a0001 | c0002 | t0007 | g0039 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01168 | hp2 | a0001 | c0002 | t0002 | g0021 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0088 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01243 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0057 | AMR | CLM | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01256 | hp2 | a0001 | c0002 | t0002 | g0160 | AMR | CLM | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01257 | hp1 | a0001 | c0002 | t0002 | g0039 | AMR | CLM | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01257 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | CLM | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01258 | hp1 | a0001 | c0002 | t0002 | g0159 | AMR | CLM | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01258 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | CLM | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0092 | AMR | CLM | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01358 | hp1 | a0001 | c0001 | t0005 | g0038 | AMR | CLM | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01361 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0100 | AMR | CLM | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01433 | hp2 | a0001 | c0002 | t0002 | g0156 | AMR | CLM | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01496 | hp1 | a0001 | c0002 | t0007 | g0003 | AMR | CLM | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0143 | EUR | IBS | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01515 | hp2 | a0001 | c0002 | t0002 | g0003 | EUR | IBS | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0014 | EUR | IBS | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01891 | hp2 | a0001 | c0003 | t0001 | g0050 | AFR | ACB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01928 | hp1 | a0001 | c0001 | t0010 | g0059 | AMR | PEL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0061 | AMR | PEL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01943 | hp1 | a0001 | c0001 | t0005 | g0038 | AMR | PEL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01943 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01952 | hp1 | a0001 | c0002 | t0002 | g0205 | AMR | PEL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01975 | hp1 | a0001 | c0001 | t0005 | g0063 | AMR | PEL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01975 | hp2 | a0001 | c0001 | t0006 | g0015 | AMR | PEL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01978 | hp2 | a0001 | c0001 | t0005 | g0148 | AMR | PEL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | PEL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02027 | hp2 | a0001 | c0002 | t0002 | g0190 | EAS | KHV | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02040 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02055 | hp1 | a0001 | c0002 | t0002 | g0153 | AFR | ACB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02055 | hp2 | a0001 | c0001 | t0003 | g0090 | AFR | ACB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02071 | hp1 | a0001 | c0002 | t0002 | g0024 | EAS | KHV | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02080 | hp2 | a0001 | c0002 | t0002 | g0024 | EAS | KHV | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02083 | hp1 | a0001 | c0002 | t0002 | g0023 | EAS | KHV | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02132 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02135 | hp1 | a0001 | c0002 | t0002 | g0192 | EAS | KHV | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02145 | hp2 | a0001 | c0002 | t0002 | g0003 | AFR | ACB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02165 | hp2 | a0001 | c0002 | t0002 | g0177 | EAS | CDX | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02257 | hp1 | a0001 | c0002 | t0002 | g0020 | AFR | ACB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02257 | hp2 | a0001 | c0001 | t0008 | g0104 | AFR | ACB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ACB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02280 | hp1 | a0001 | c0002 | t0002 | g0178 | AFR | ACB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02280 | hp2 | a0001 | c0002 | t0002 | g0161 | AFR | ACB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02300 | hp1 | a0001 | c0002 | t0007 | g0003 | AMR | PEL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02451 | hp1 | a0001 | c0002 | t0002 | g0040 | AFR | ACB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02451 | hp2 | a0001 | c0002 | t0002 | g0174 | AFR | ACB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02523 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02572 | hp1 | a0001 | c0002 | t0002 | g0040 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02572 | hp2 | a0001 | c0001 | t0011 | g0009 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02602 | hp1 | a0001 | c0002 | t0002 | g0157 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02615 | hp1 | a0001 | c0004 | t0001 | g0012 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02615 | hp2 | a0001 | c0003 | t0001 | g0027 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02622 | hp2 | a0001 | c0002 | t0002 | g0170 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02630 | hp1 | a0001 | c0002 | t0002 | g0003 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02630 | hp2 | a0001 | c0004 | t0001 | g0026 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0086 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02647 | hp2 | a0001 | c0003 | t0001 | g0053 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02683 | hp1 | a0001 | c0002 | t0002 | g0021 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02698 | hp1 | a0001 | c0002 | t0002 | g0201 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02698 | hp2 | a0001 | c0001 | t0004 | g0071 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0089 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02723 | hp2 | a0001 | c0002 | t0002 | g0011 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02735 | hp1 | a0001 | c0002 | t0002 | g0176 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02809 | hp1 | a0001 | c0002 | t0002 | g0164 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02809 | hp2 | a0001 | c0002 | t0002 | g0171 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02818 | hp2 | a0001 | c0002 | t0002 | g0167 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02886 | hp1 | a0001 | c0002 | t0013 | g0054 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0033 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0145 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02896 | hp2 | a0001 | c0002 | t0002 | g0168 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02922 | hp1 | a0001 | c0002 | t0002 | g0154 | AFR | ESN | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02922 | hp2 | a0001 | c0002 | t0002 | g0020 | AFR | ESN | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02965 | hp1 | a0001 | c0003 | t0001 | g0049 | AFR | ESN | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ESN | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02970 | hp1 | a0001 | c0003 | t0001 | g0025 | AFR | ESN | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02970 | hp2 | a0001 | c0001 | t0006 | g0015 | AFR | ESN | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0058 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0077 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03041 | hp1 | a0001 | c0004 | t0001 | g0012 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0091 | AFR | MSL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03098 | hp2 | a0001 | c0001 | t0006 | g0106 | AFR | MSL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | ESN | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0146 | AFR | ESN | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0078 | AFR | ESN | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03195 | hp1 | a0001 | c0002 | t0002 | g0020 | AFR | ESN | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03195 | hp2 | a0001 | c0002 | t0002 | g0155 | AFR | ESN | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03209 | hp2 | a0001 | c0002 | t0002 | g0019 | AFR | MSL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03225 | hp1 | a0001 | c0003 | t0001 | g0052 | AFR | MSL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0070 | AFR | MSL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03239 | hp1 | a0001 | c0001 | t0005 | g0004 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03239 | hp2 | a0001 | c0002 | t0002 | g0151 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03453 | hp1 | a0001 | c0004 | t0001 | g0046 | AFR | MSL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0085 | AFR | MSL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0204 | AFR | MSL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03486 | hp2 | a0001 | c0002 | t0002 | g0011 | AFR | MSL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03490 | hp1 | a0001 | c0001 | t0004 | g0074 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03490 | hp2 | a0001 | c0001 | t0004 | g0202 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0014 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0094 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03516 | hp1 | a0001 | c0004 | t0001 | g0026 | AFR | ESN | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03540 | hp1 | a0001 | c0003 | t0001 | g0048 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03540 | hp2 | a0001 | c0002 | t0002 | g0019 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | MSL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0103 | AFR | MSL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03654 | hp1 | a0001 | c0002 | t0002 | g0158 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0055 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0028 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0082 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0030 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0030 | SAS | BEB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03834 | hp2 | a0001 | c0002 | t0002 | g0150 | SAS | BEB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03942 | hp2 | a0001 | c0001 | t0004 | g0107 | SAS | BEB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | STU | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | STU | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG04184 | hp1 | a0001 | c0001 | t0004 | g0098 | SAS | BEB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18522 | hp1 | a0001 | c0002 | t0002 | g0186 | AFR | YRI | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18522 | hp2 | a0001 | c0001 | t0006 | g0015 | AFR | YRI | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18612 | hp1 | a0001 | c0002 | t0002 | g0181 | EAS | CHB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18906 | hp1 | a0001 | c0003 | t0001 | g0025 | AFR | YRI | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18906 | hp2 | a0001 | c0002 | t0002 | g0011 | AFR | YRI | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18941 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18942 | hp1 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18943 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18946 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18946 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18947 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18947 | hp2 | a0001 | c0002 | t0002 | g0195 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18948 | hp1 | a0001 | c0001 | t0004 | g0083 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18951 | hp2 | a0001 | c0002 | t0002 | g0189 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18956 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18956 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18957 | hp1 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18960 | hp1 | a0001 | c0002 | t0002 | g0198 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18961 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18963 | hp2 | a0001 | c0002 | t0002 | g0184 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18964 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18965 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18966 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18967 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18967 | hp2 | a0001 | c0002 | t0002 | g0182 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18969 | hp1 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18969 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18970 | hp2 | a0001 | c0002 | t0002 | g0197 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18971 | hp2 | a0001 | c0001 | t0009 | g0131 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18973 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18979 | hp1 | a0001 | c0002 | t0002 | g0199 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18983 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18988 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18989 | hp2 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18990 | hp2 | a0001 | c0001 | t0012 | g0005 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18991 | hp2 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18993 | hp1 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18994 | hp2 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18995 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18997 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA18998 | hp2 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19001 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19003 | hp2 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19005 | hp2 | a0001 | c0002 | t0002 | g0187 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19009 | hp1 | a0001 | c0002 | t0002 | g0193 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19012 | hp2 | a0001 | c0002 | t0002 | g0185 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19030 | hp1 | a0001 | c0002 | t0002 | g0019 | AFR | LWK | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | LWK | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19043 | hp1 | a0001 | c0002 | t0002 | g0172 | AFR | LWK | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19043 | hp2 | a0001 | c0002 | t0002 | g0169 | AFR | LWK | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19054 | hp1 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19055 | hp2 | a0001 | c0002 | t0002 | g0152 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19056 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19062 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19064 | hp1 | a0001 | c0002 | t0002 | g0188 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19066 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19068 | hp1 | a0001 | c0002 | t0002 | g0180 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19077 | hp2 | a0001 | c0002 | t0002 | g0200 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19079 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19080 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19082 | hp2 | a0001 | c0002 | t0002 | g0196 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19083 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19084 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19086 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19086 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19087 | hp2 | a0001 | c0002 | t0002 | g0183 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19090 | hp1 | a0001 | c0002 | t0002 | g0194 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19091 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19240 | hp1 | a0001 | c0003 | t0001 | g0027 | AFR | YRI | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA19240 | hp2 | a0001 | c0001 | t0008 | g0105 | AFR | YRI | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0072 | AFR | ASW | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0060 | EUR | TSI | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA20805 | hp2 | a0001 | c0002 | t0002 | g0003 | EUR | TSI | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | GIH | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0031 | SAS | GIH | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG01123 | hp2 | a0001 | c0001 | t0003 | g0081 | AMR | CLM | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02109 | hp1 | a0001 | c0004 | t0001 | g0047 | AFR | ACB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02109 | hp2 | a0001 | c0002 | t0002 | g0011 | AFR | ACB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02486 | hp1 | a0001 | c0002 | t0002 | g0166 | AFR | ACB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02486 | hp2 | a0001 | c0004 | t0001 | g0045 | AFR | ACB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02559 | hp1 | a0001 | c0002 | t0002 | g0191 | AFR | ACB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ACB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03471 | hp1 | a0001 | c0003 | t0001 | g0051 | AFR | MSL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG03471 | hp2 | a0001 | c0004 | t0001 | g0012 | AFR | MSL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | USA | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0097 | AFR | USA | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
NA20300 | hp2 | a0002 | c0005 | t0003 | g0033 | AFR | USA | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0002 | g0165 | REF | REF | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:100713753
|
G | A | 1 | a0002 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.68G>A | p.Arg23Gln | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/8 | 339/1907 | 68/1203 | 23/400 | chr3 | 100713753 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:100732644
|
G | A | 2 | a0001c0003a0001c0004 | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
synonymous_variant | LOW | c.552G>A | p.Ala184Ala | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/8 | 823/1907 | 552/1203 | 184/400 | chr3 | 100732644 | ||
chr3:100736658
|
C | A | 1 | a0001c0004 | 9 | HG00735.hp1 HG02109.hp1 HG02486.hp2 others(6): Show |
synonymous_variant | LOW | c.663C>A | p.Gly221Gly | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/8 | 934/1907 | 663/1203 | 221/400 | chr3 | 100736658 | ||
chr3:100748174
|
T | C | 4 | a0001c0001a0001c0003a0001c0004others(1): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
synonymous_variant | LOW | c.846T>C | p.Pro282Pro | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 8/8 | 1117/1907 | 846/1203 | 282/400 | chr3 | 100748174 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:100709512
|
A | G | 1 | a0001c0002t0007 | 3 | HG01167.hp2 HG01496.hp1 HG02300.hp1 |
5_prime_UTR_variant | MODIFIER | c.-253A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/8 | 4174 | chr3 | 100709512 | |||||
chr3:100709515
|
T | G | 1 | a0001c0001t0009 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-250T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/8 | 4171 | chr3 | 100709515 | |||||
chr3:100709616
|
G | C | 13 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(10): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
5_prime_UTR_variant | MODIFIER | c.-149G>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/8 | 4070 | chr3 | 100709616 | |||||
chr3:100709629
|
C | T | 1 | a0001c0001t0012 | 1 | NA18990.hp2 | 5_prime_UTR_variant | MODIFIER | c.-136C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/8 | 4057 | chr3 | 100709629 | |||||
chr3:100709633
|
C | G | 1 | a0001c0001t0011 | 1 | HG02572.hp2 | 5_prime_UTR_variant | MODIFIER | c.-132C>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/8 | 4053 | chr3 | 100709633 | |||||
chr3:100748556
|
G | A | 1 | a0001c0002t0013 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*25G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 8/8 | 25 | chr3 | 100748556 | |||||
chr3:100748640
|
A | AT | 1 | a0001c0001t0006 | 4 | HG01975.hp2 HG02970.hp2 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*115dupT | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 8/8 | 116 | INFO_REALIGN_3_PRIME | chr3 | 100748640 | ||||
chr3:100748751
|
ACT | A | 1 | a0001c0001t0005 | 6 | HG01167.hp1 HG01358.hp1 HG01943.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*221_*222delCT | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 8/8 | 221 | chr3 | 100748751 | |||||
chr3:100748803
|
T | G | 1 | a0001c0001t0008 | 2 | HG02257.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*272T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 8/8 | 272 | chr3 | 100748803 | |||||
chr3:100748813
|
C | T | 1 | a0001c0001t0010 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*282C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 8/8 | 282 | chr3 | 100748813 | |||||
chr3:100748829
|
G | A | 1 | a0001c0001t0004 | 10 | HG00099.hp2 HG00438.hp1 HG01257.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*298G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 8/8 | 298 | chr3 | 100748829 | |||||
chr3:100748832
|
A | T | 8 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(5): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*301A>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 8/8 | 301 | chr3 | 100748832 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:100709743
|
G | C | 1 | a0001c0002t0002g0043 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-44+22G>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100709743 | ||||||
chr3:100709784
|
C | G | 1 | a0001c0004t0001g0207 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-44+63C>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100709784 | ||||||
chr3:100709785
|
G | T | 1 | a0001c0001t0001g0206 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-44+64G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100709785 | ||||||
chr3:100709800
|
T | C | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-44+79T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100709800 | ||||||
chr3:100709838
|
G | C | 1 | a0001c0001t0003g0028 | 2 | HG00280.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-44+117G>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100709838 | ||||||
chr3:100709846
|
T | TGGAGGGA others(10): Show |
3 | a0001c0001t0001g0203a0001c0001t0003g0204a0001c0002t0002g0205 | 3 | HG01952.hp1 HG02683.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-44+153_-44+169dup others(17): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 100709846 | |||||
chr3:100709846
|
TGGAGGGA others(10): Show |
T | 1 | a0001c0002t0013g0054 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-44+153_-44+169del others(17): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 100709846 | |||||
chr3:100709905
|
A | C | 1 | a0001c0001t0004g0202 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-44+184A>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100709905 | ||||||
chr3:100710003
|
G | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(140): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.-44+282G>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100710003 | ||||||
chr3:100710127
|
T | C | 1 | a0001c0003t0001g0025 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-44+406T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100710127 | ||||||
chr3:100710185
|
G | T | 1 | a0001c0001t0001g0149 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-44+464G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100710185 | ||||||
chr3:100710205
|
C | T | 1 | a0001c0002t0002g0201 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-44+484C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100710205 | ||||||
chr3:100710266
|
C | CT | 13 | a0001c0003t0001g0027a0001c0003t0001g0048a0001c0003t0001g0049others(10): Show | 17 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-44+548dupT | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 100710266 | |||||
chr3:100710295
|
A | G | 7 | a0001c0003t0001g0027a0001c0003t0001g0048a0001c0003t0001g0049others(4): Show | 8 | HG01891.hp2 HG02615.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-44+574A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100710295 | ||||||
chr3:100710334
|
A | G | 1 | a0001c0003t0001g0044 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-44+613A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100710334 | ||||||
chr3:100710352
|
A | C | 1 | a0001c0002t0002g0200 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-44+631A>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100710352 | ||||||
chr3:100710521
|
C | G | 1 | a0001c0001t0003g0204 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-44+800C>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100710521 | ||||||
chr3:100710736
|
G | A | 1 | a0001c0001t0001g0029 | 2 | NA19064.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-44+1015G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100710736 | ||||||
chr3:100710737
|
C | A | 1 | a0001c0003t0001g0044 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-44+1016C>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100710737 | ||||||
chr3:100710864
|
G | A | 1 | a0001c0003t0001g0044 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-44+1143G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100710864 | ||||||
chr3:100710881
|
G | A | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-44+1160G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100710881 | ||||||
chr3:100710915
|
G | A | 2 | a0001c0001t0003g0030a0001c0001t0003g0055 | 3 | HG03654.hp2 HG03704.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.-44+1194G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100710915 | ||||||
chr3:100711008
|
C | T | 2 | a0001c0001t0005g0038a0001c0001t0005g0148 | 3 | HG01358.hp1 HG01943.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.-44+1287C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711008 | ||||||
chr3:100711051
|
C | T | 28 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0022others(25): Show | 58 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.-44+1330C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711051 | ||||||
chr3:100711101
|
C | G | 2 | a0001c0002t0002g0178a0001c0002t0002g0179 | 2 | HG01099.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.-44+1380C>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711101 | ||||||
chr3:100711103
|
A | AT | 12 | a0001c0001t0001g0147a0001c0001t0003g0007a0001c0001t0003g0145others(9): Show | 19 | HG00735.hp1 HG02109.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.-44+1397dupT | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 100711103 | |||||
chr3:100711103
|
A | ATT | 7 | a0001c0003t0001g0027a0001c0003t0001g0048a0001c0003t0001g0049others(4): Show | 8 | HG01891.hp2 HG02615.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-44+1396_-44+1397d others(4): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 100711103 | |||||
chr3:100711103
|
AT | A | 64 | a0001c0001t0001g0099a0001c0001t0003g0004a0001c0001t0003g0008others(61): Show | 86 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.-44+1397delT | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 100711103 | |||||
chr3:100711153
|
T | G | 24 | a0001c0001t0003g0004a0001c0001t0003g0013a0001c0001t0003g0028others(21): Show | 39 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.-44+1432T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711153 | ||||||
chr3:100711221
|
G | C | 6 | a0001c0004t0001g0012a0001c0004t0001g0026a0001c0004t0001g0045others(3): Show | 9 | HG00735.hp1 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-44+1500G>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711221 | ||||||
chr3:100711234
|
C | T | 1 | a0001c0003t0001g0053 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-44+1513C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711234 | ||||||
chr3:100711257
|
G | A | 1 | a0001c0003t0001g0044 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-44+1536G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711257 | ||||||
chr3:100711275
|
G | T | 1 | a0001c0002t0002g0177 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-44+1554G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711275 | ||||||
chr3:100711334
|
C | T | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-44+1613C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711334 | ||||||
chr3:100711347
|
C | T | 1 | a0001c0002t0002g0176 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-44+1626C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711347 | ||||||
chr3:100711378
|
G | A | 3 | a0001c0001t0003g0007a0001c0001t0003g0145a0001c0001t0003g0146 | 7 | HG02258.hp2 HG02559.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-44+1657G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711378 | ||||||
chr3:100711394
|
C | T | 1 | a0001c0001t0003g0100 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-44+1673C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711394 | ||||||
chr3:100711492
|
T | A | 1 | a0001c0001t0001g0102 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-44+1771T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711492 | ||||||
chr3:100711664
|
G | A | 6 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0058others(3): Show | 6 | HG00323.hp1 HG01255.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.-44+1943G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711664 | ||||||
chr3:100711817
|
T | TTA | 6 | a0001c0004t0001g0012a0001c0004t0001g0026a0001c0004t0001g0045others(3): Show | 9 | HG00735.hp1 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-43-1826_-43-1825i others(4): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711817 | ||||||
chr3:100711818
|
A | C | 6 | a0001c0004t0001g0012a0001c0004t0001g0026a0001c0004t0001g0045others(3): Show | 9 | HG00735.hp1 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-43-1825A>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711818 | ||||||
chr3:100711821
|
T | C | 6 | a0001c0004t0001g0012a0001c0004t0001g0026a0001c0004t0001g0045others(3): Show | 9 | HG00735.hp1 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-43-1822T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711821 | ||||||
chr3:100711831
|
G | A | 73 | a0001c0001t0003g0004a0001c0001t0003g0007a0001c0001t0003g0008others(70): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.-43-1812G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711831 | ||||||
chr3:100711854
|
T | C | 2 | a0001c0002t0002g0043a0001c0002t0002g0180 | 2 | NA18994.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.-43-1789T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711854 | ||||||
chr3:100711893
|
C | A | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-43-1750C>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711893 | ||||||
chr3:100711924
|
G | A | 28 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0022others(25): Show | 58 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.-43-1719G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711924 | ||||||
chr3:100711967
|
C | T | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-43-1676C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711967 | ||||||
chr3:100711995
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-43-1648T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711995 | ||||||
chr3:100712044
|
C | T | 1 | a0001c0001t0004g0098 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-43-1599C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100712044 | ||||||
chr3:100712171
|
T | G | 13 | a0001c0003t0001g0027a0001c0003t0001g0048a0001c0003t0001g0049others(10): Show | 17 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-43-1472T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100712171 | ||||||
chr3:100712369
|
T | G | 1 | a0001c0001t0003g0204 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-43-1274T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100712369 | ||||||
chr3:100712662
|
G | A | 1 | a0001c0003t0001g0048 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-43-981G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100712662 | ||||||
chr3:100712762
|
A | C | 1 | a0001c0002t0002g0176 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-43-881A>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100712762 | ||||||
chr3:100712804
|
TAAATTAG others(74): Show |
T | 1 | a0001c0001t0001g0206 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-43-836_-43-756del others(81): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 100712804 | |||||
chr3:100712851
|
G | T | 1 | a0001c0001t0003g0097 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-43-792G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100712851 | ||||||
chr3:100713001
|
G | C | 14 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0048others(11): Show | 19 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.-43-642G>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100713001 | ||||||
chr3:100713108
|
G | A | 1 | a0001c0001t0003g0103 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-43-535G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100713108 | ||||||
chr3:100713140
|
T | A | 1 | a0001c0001t0001g0206 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-43-503T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100713140 | ||||||
chr3:100713242
|
C | T | 1 | a0001c0001t0001g0144 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-43-401C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100713242 | ||||||
chr3:100713329
|
A | C | 1 | a0001c0002t0002g0175 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-43-314A>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100713329 | ||||||
chr3:100713393
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-43-250G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100713393 | ||||||
chr3:100713449
|
A | G | 1 | a0001c0001t0003g0096 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-43-194A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100713449 | ||||||
chr3:100713482
|
A | G | 3 | a0001c0001t0003g0007a0001c0001t0003g0145a0001c0001t0003g0146 | 7 | HG02258.hp2 HG02559.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43-161A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100713482 | ||||||
chr3:100713493
|
A | C | 1 | a0001c0003t0001g0052 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-43-150A>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100713493 | ||||||
chr3:100713554
|
G | A | 1 | a0001c0002t0013g0054 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-43-89G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100713554 | ||||||
chr3:100713570
|
CATCTA | C | 14 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0048others(11): Show | 19 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.-43-70_-43-66delCT others(3): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 100713570 | |||||
chr3:100713902
|
C | CCT | 13 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0048others(10): Show | 18 | HG00735.hp1 HG01891.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.184+33_184+34insCT | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100713902 | ||||||
chr3:100713902
|
C | CT | 4 | a0001c0001t0001g0206a0001c0001t0003g0007a0001c0001t0003g0101others(1): Show | 8 | HG02258.hp2 HG02559.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.184+38dupT | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 100713902 | |||||
chr3:100713907
|
T | A | 1 | a0001c0002t0002g0151 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.184+38T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100713907 | ||||||
chr3:100713907
|
T | TA | 4 | a0001c0002t0002g0022a0001c0002t0002g0043a0001c0002t0002g0152others(1): Show | 6 | NA18989.hp2 NA18993.hp1 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.184+55dupA | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 100713907 | |||||
chr3:100713907
|
TA | T | 12 | a0001c0001t0001g0037a0001c0001t0001g0143a0001c0001t0003g0069others(9): Show | 17 | HG00323.hp2 HG00558.hp2 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.184+55delA | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 100713907 | |||||
chr3:100713908
|
A | T | 120 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(117): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.184+39A>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100713908 | ||||||
chr3:100713909
|
A | T | 6 | a0001c0001t0001g0037a0001c0001t0001g0143a0001c0001t0003g0069others(3): Show | 7 | HG00323.hp2 HG01168.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.184+40A>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100713909 | ||||||
chr3:100713923
|
A | G | 14 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0048others(11): Show | 19 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.184+54A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100713923 | ||||||
chr3:100714131
|
C | T | 73 | a0001c0001t0003g0004a0001c0001t0003g0007a0001c0001t0003g0008others(70): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.184+262C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100714131 | ||||||
chr3:100714212
|
A | G | 1 | a0001c0001t0003g0094 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.184+343A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100714212 | ||||||
chr3:100714374
|
G | A | 1 | a0001c0001t0004g0202 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.184+505G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100714374 | ||||||
chr3:100714424
|
C | T | 1 | a0001c0002t0002g0173 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.184+555C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100714424 | ||||||
chr3:100714436
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.184+567C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100714436 | ||||||
chr3:100714460
|
A | G | 1 | a0001c0002t0002g0197 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.184+591A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100714460 | ||||||
chr3:100714567
|
AT | A | 76 | a0001c0001t0001g0010a0001c0001t0001g0034a0001c0001t0001g0206others(73): Show | 108 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.184+706delT | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 100714567 | |||||
chr3:100714585
|
A | G | 73 | a0001c0001t0003g0004a0001c0001t0003g0007a0001c0001t0003g0008others(70): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.184+716A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100714585 | ||||||
chr3:100714748
|
T | C | 25 | a0001c0002t0002g0003a0001c0002t0002g0021a0001c0002t0002g0039others(22): Show | 39 | HG00597.hp1 HG00639.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.184+879T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100714748 | ||||||
chr3:100714953
|
T | C | 88 | a0001c0001t0003g0004a0001c0001t0003g0007a0001c0001t0003g0008others(85): Show | 121 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.184+1084T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100714953 | ||||||
chr3:100715003
|
G | T | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.184+1134G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100715003 | ||||||
chr3:100715307
|
A | G | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.184+1438A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100715307 | ||||||
chr3:100715379
|
G | A | 2 | a0001c0004t0001g0012a0001c0004t0001g0207 | 4 | HG00735.hp1 HG02615.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.184+1510G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100715379 | ||||||
chr3:100715498
|
G | A | 168 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(165): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.184+1629G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100715498 | ||||||
chr3:100715662
|
T | C | 1 | a0001c0002t0002g0174 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.184+1793T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100715662 | ||||||
chr3:100715674
|
A | G | 1 | a0001c0003t0001g0044 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.184+1805A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100715674 | ||||||
chr3:100715687
|
T | G | 2 | a0001c0001t0008g0104a0001c0001t0008g0105 | 2 | HG02257.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.184+1818T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100715687 | ||||||
chr3:100715796
|
T | C | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.184+1927T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100715796 | ||||||
chr3:100715933
|
T | A | 13 | a0001c0003t0001g0027a0001c0003t0001g0048a0001c0003t0001g0049others(10): Show | 17 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.184+2064T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100715933 | ||||||
chr3:100715983
|
A | G | 1 | a0001c0001t0003g0204 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.184+2114A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100715983 | ||||||
chr3:100716089
|
T | C | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.184+2220T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100716089 | ||||||
chr3:100716101
|
A | T | 1 | a0001c0001t0001g0206 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.184+2232A>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100716101 | ||||||
chr3:100716128
|
A | T | 3 | a0001c0002t0002g0006a0001c0002t0002g0195a0001c0002t0002g0196 | 8 | NA18946.hp1 NA18947.hp2 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.184+2259A>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100716128 | ||||||
chr3:100716278
|
T | G | 5 | a0001c0002t0002g0006a0001c0002t0002g0041a0001c0002t0002g0195others(2): Show | 11 | NA18946.hp1 NA18947.hp2 NA18957.hp1 others(8): Show |
intron_variant | MODIFIER | c.184+2409T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100716278 | ||||||
chr3:100716383
|
A | G | 73 | a0001c0001t0003g0004a0001c0001t0003g0007a0001c0001t0003g0008others(70): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.184+2514A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100716383 | ||||||
chr3:100716530
|
G | T | 2 | a0001c0001t0001g0140a0001c0001t0001g0141 | 2 | HG01928.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.184+2661G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100716530 | ||||||
chr3:100716575
|
T | C | 128 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(125): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.184+2706T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100716575 | ||||||
chr3:100716672
|
C | T | 2 | a0001c0001t0001g0036a0001c0001t0001g0139 | 3 | HG01109.hp2 HG02602.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.184+2803C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100716672 | ||||||
chr3:100716739
|
T | C | 4 | a0001c0002t0002g0181a0001c0002t0002g0182a0001c0002t0002g0183others(1): Show | 4 | NA18612.hp1 NA18963.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.184+2870T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100716739 | ||||||
chr3:100716927
|
C | G | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.185-3048C>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100716927 | ||||||
chr3:100717576
|
A | G | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.185-2399A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100717576 | ||||||
chr3:100717579
|
GT | G | 142 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(139): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.185-2381delT | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 100717579 | |||||
chr3:100717579
|
GTT | G | 3 | a0001c0001t0003g0007a0001c0001t0003g0145a0001c0001t0003g0146 | 7 | HG02258.hp2 HG02559.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.185-2382_185-2381d others(4): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 100717579 | |||||
chr3:100717647
|
T | A | 1 | a0001c0001t0001g0111 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.185-2328T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100717647 | ||||||
chr3:100717651
|
T | A | 1 | a0001c0001t0001g0206 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.185-2324T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100717651 | ||||||
chr3:100717687
|
T | G | 55 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(52): Show | 106 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.185-2288T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100717687 | ||||||
chr3:100717694
|
A | G | 1 | a0001c0003t0001g0052 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.185-2281A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100717694 | ||||||
chr3:100717781
|
G | A | 14 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0048others(11): Show | 19 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.185-2194G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100717781 | ||||||
chr3:100717803
|
T | A | 1 | a0001c0003t0001g0044 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.185-2172T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100717803 | ||||||
chr3:100717838
|
T | TTGAC | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.185-2135_185-2134i others(6): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 100717838 | |||||
chr3:100717868
|
T | A | 1 | a0001c0001t0001g0206 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.185-2107T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100717868 | ||||||
chr3:100717904
|
G | C | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.185-2071G>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100717904 | ||||||
chr3:100717981
|
G | A | 1 | a0001c0002t0002g0164 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.185-1994G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100717981 | ||||||
chr3:100718054
|
A | G | 1 | a0001c0001t0003g0092 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.185-1921A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100718054 | ||||||
chr3:100718229
|
T | C | 1 | a0001c0001t0001g0112 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.185-1746T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100718229 | ||||||
chr3:100718275
|
CTG | C | 14 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0048others(11): Show | 19 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.185-1699_185-1698d others(4): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100718275 | ||||||
chr3:100718288
|
C | T | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.185-1687C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100718288 | ||||||
chr3:100718305
|
A | G | 5 | a0001c0001t0003g0070a0001c0001t0003g0088a0001c0001t0003g0089others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.185-1670A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100718305 | ||||||
chr3:100718549
|
G | GT | 12 | a0001c0002t0002g0011a0001c0002t0002g0020a0001c0002t0002g0164others(9): Show | 17 | HG01099.hp1 HG02109.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.185-1400dupT | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 100718549 | |||||
chr3:100718549
|
GT | G | 76 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0016others(73): Show | 161 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.185-1400delT | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 100718549 | |||||
chr3:100718549
|
GTT | G | 7 | a0001c0001t0001g0114a0001c0001t0003g0065a0001c0001t0003g0090others(4): Show | 7 | HG00280.hp1 HG01167.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.185-1401_185-1400d others(4): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 100718549 | |||||
chr3:100718549
|
GTTT | G | 17 | a0001c0001t0001g0113a0001c0001t0003g0030a0001c0001t0003g0031others(14): Show | 19 | HG01106.hp2 HG01243.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.185-1402_185-1400d others(5): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 100718549 | |||||
chr3:100718549
|
GTTTT | G | 60 | a0001c0001t0003g0004a0001c0001t0003g0008a0001c0001t0003g0009others(57): Show | 85 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.185-1403_185-1400d others(6): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 100718549 | |||||
chr3:100718549
|
GTTTTTT | G | 6 | a0001c0001t0003g0007a0001c0001t0003g0103a0001c0001t0003g0145others(3): Show | 12 | HG01975.hp2 HG02258.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.185-1405_185-1400d others(8): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 100718549 | |||||
chr3:100718555
|
T | G | 1 | a0001c0003t0001g0044 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.185-1420T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100718555 | ||||||
chr3:100718557
|
T | G | 14 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0048others(11): Show | 19 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.185-1418T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100718557 | ||||||
chr3:100718600
|
T | C | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.185-1375T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100718600 | ||||||
chr3:100718618
|
G | T | 213 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(210): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.185-1357G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100718618 | ||||||
chr3:100718645
|
C | A | 1 | a0001c0001t0001g0206 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.185-1330C>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100718645 | ||||||
chr3:100718698
|
T | C | 1 | a0001c0003t0001g0044 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.185-1277T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100718698 | ||||||
chr3:100718705
|
A | G | 1 | a0001c0001t0009g0131 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.185-1270A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100718705 | ||||||
chr3:100718966
|
G | A | 64 | a0001c0001t0003g0004a0001c0001t0003g0008a0001c0001t0003g0009others(61): Show | 86 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.185-1009G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100718966 | ||||||
chr3:100719048
|
A | G | 88 | a0001c0001t0003g0004a0001c0001t0003g0007a0001c0001t0003g0008others(85): Show | 121 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.185-927A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100719048 | ||||||
chr3:100719082
|
G | A | 2 | a0001c0001t0006g0015a0001c0001t0006g0106 | 4 | HG01975.hp2 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.185-893G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100719082 | ||||||
chr3:100719083
|
T | G | 2 | a0001c0001t0003g0007a0001c0001t0003g0145 | 6 | HG02258.hp2 HG02559.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.185-892T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100719083 | ||||||
chr3:100719137
|
C | T | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.185-838C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100719137 | ||||||
chr3:100719177
|
G | A | 1 | a0001c0001t0003g0145 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.185-798G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100719177 | ||||||
chr3:100719360
|
G | A | 1 | a0001c0001t0004g0083 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.185-615G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100719360 | ||||||
chr3:100719410
|
A | G | 6 | a0001c0004t0001g0012a0001c0004t0001g0026a0001c0004t0001g0045others(3): Show | 9 | HG00735.hp1 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.185-565A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100719410 | ||||||
chr3:100719426
|
A | G | 1 | a0001c0003t0001g0051 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.185-549A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100719426 | ||||||
chr3:100719515
|
G | C | 13 | a0001c0003t0001g0027a0001c0003t0001g0048a0001c0003t0001g0049others(10): Show | 17 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.185-460G>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100719515 | ||||||
chr3:100719523
|
A | T | 1 | a0001c0001t0001g0206 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.185-452A>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100719523 | ||||||
chr3:100719710
|
G | A | 1 | a0001c0001t0005g0148 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.185-265G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100719710 | ||||||
chr3:100719850
|
A | C | 1 | a0001c0001t0003g0082 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.185-125A>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100719850 | ||||||
chr3:100719940
|
A | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(51): Show | 105 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.185-35A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100719940 | ||||||
chr3:100720280
|
TG | T | 54 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(51): Show | 105 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.268+223delG | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100720280 | ||||||
chr3:100720347
|
A | G | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.268+289A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100720347 | ||||||
chr3:100720612
|
G | A | 13 | a0001c0003t0001g0027a0001c0003t0001g0048a0001c0003t0001g0049others(10): Show | 17 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.268+554G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100720612 | ||||||
chr3:100720618
|
C | T | 1 | a0001c0002t0002g0194 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.268+560C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100720618 | ||||||
chr3:100720628
|
C | T | 3 | a0001c0001t0003g0007a0001c0001t0003g0145a0001c0001t0003g0146 | 7 | HG02258.hp2 HG02559.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.268+570C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100720628 | ||||||
chr3:100720654
|
T | G | 1 | a0001c0003t0001g0025 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.268+596T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100720654 | ||||||
chr3:100720814
|
C | T | 2 | a0001c0001t0008g0104a0001c0001t0008g0105 | 2 | HG02257.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.268+756C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100720814 | ||||||
chr3:100720885
|
T | G | 1 | a0001c0002t0002g0166 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.268+827T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100720885 | ||||||
chr3:100720948
|
T | A | 1 | a0001c0001t0001g0206 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.268+890T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100720948 | ||||||
chr3:100720950
|
A | T | 1 | a0001c0001t0001g0206 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.268+892A>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100720950 | ||||||
chr3:100720979
|
G | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(139): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.268+921G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100720979 | ||||||
chr3:100721012
|
G | A | 12 | a0001c0003t0001g0027a0001c0003t0001g0048a0001c0003t0001g0049others(9): Show | 16 | HG00735.hp1 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.268+954G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100721012 | ||||||
chr3:100721013
|
T | A | 1 | a0001c0003t0001g0050 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.268+955T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100721013 | ||||||
chr3:100721211
|
C | T | 1 | a0001c0001t0003g0013 | 3 | NA18943.hp2 NA19057.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.268+1153C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100721211 | ||||||
chr3:100721227
|
C | T | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.268+1169C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100721227 | ||||||
chr3:100721505
|
T | C | 1 | a0001c0001t0004g0071 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.268+1447T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100721505 | ||||||
chr3:100721587
|
A | G | 2 | a0001c0001t0006g0015a0001c0001t0006g0106 | 4 | HG01975.hp2 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.268+1529A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100721587 | ||||||
chr3:100721826
|
A | G | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.268+1768A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100721826 | ||||||
chr3:100721980
|
A | G | 2 | a0001c0001t0006g0015a0001c0001t0006g0106 | 4 | HG01975.hp2 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.268+1922A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100721980 | ||||||
chr3:100721993
|
T | A | 1 | a0001c0002t0002g0168 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.268+1935T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100721993 | ||||||
chr3:100722107
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.268+2049C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100722107 | ||||||
chr3:100722176
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.268+2118A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100722176 | ||||||
chr3:100722192
|
A | G | 28 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0022others(25): Show | 58 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.268+2134A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100722192 | ||||||
chr3:100722364
|
G | A | 1 | a0001c0003t0001g0044 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.268+2306G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100722364 | ||||||
chr3:100722419
|
A | G | 127 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(124): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.268+2361A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100722419 | ||||||
chr3:100722496
|
A | G | 1 | a0001c0001t0003g0204 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.268+2438A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100722496 | ||||||
chr3:100722635
|
G | A | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.268+2577G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100722635 | ||||||
chr3:100722742
|
A | C | 1 | a0001c0001t0003g0146 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.268+2684A>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100722742 | ||||||
chr3:100722750
|
A | G | 1 | a0001c0001t0010g0059 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.268+2692A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100722750 | ||||||
chr3:100722872
|
T | C | 26 | a0001c0001t0001g0142a0001c0002t0002g0003a0001c0002t0002g0021others(23): Show | 40 | HG00597.hp1 HG00639.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.268+2814T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100722872 | ||||||
chr3:100723015
|
T | G | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.268+2957T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100723015 | ||||||
chr3:100723058
|
A | G | 2 | a0001c0001t0003g0009a0001c0001t0011g0009 | 4 | HG01106.hp1 HG02572.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.268+3000A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100723058 | ||||||
chr3:100723441
|
A | C | 2 | a0001c0001t0001g0130a0001c0001t0001g0136 | 2 | HG01891.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.268+3383A>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100723441 | ||||||
chr3:100723475
|
T | A | 1 | a0001c0001t0003g0072 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.268+3417T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100723475 | ||||||
chr3:100723542
|
A | G | 26 | a0001c0001t0001g0142a0001c0002t0002g0003a0001c0002t0002g0021others(23): Show | 40 | HG00597.hp1 HG00639.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.268+3484A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100723542 | ||||||
chr3:100723604
|
T | C | 1 | a0001c0003t0001g0025 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.268+3546T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100723604 | ||||||
chr3:100723634
|
A | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(51): Show | 105 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.268+3576A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100723634 | ||||||
chr3:100723666
|
T | C | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.268+3608T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100723666 | ||||||
chr3:100723673
|
A | G | 2 | a0001c0002t0002g0159a0001c0002t0002g0160 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.268+3615A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100723673 | ||||||
chr3:100723686
|
T | C | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.268+3628T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100723686 | ||||||
chr3:100723749
|
T | G | 3 | a0001c0001t0003g0084a0001c0001t0003g0093a0001c0001t0003g0096 | 3 | NA18947.hp1 NA18962.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.268+3691T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100723749 | ||||||
chr3:100723769
|
G | A | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.268+3711G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100723769 | ||||||
chr3:100723814
|
A | G | 7 | a0001c0003t0001g0027a0001c0003t0001g0048a0001c0003t0001g0049others(4): Show | 8 | HG01891.hp2 HG02615.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.268+3756A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100723814 | ||||||
chr3:100723831
|
G | GT | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0003g0007others(1): Show | 8 | HG02258.hp2 HG02559.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.268+3786dupT | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 100723831 | |||||
chr3:100723845
|
C | G | 6 | a0001c0004t0001g0012a0001c0004t0001g0026a0001c0004t0001g0045others(3): Show | 9 | HG00735.hp1 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.268+3787C>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100723845 | ||||||
chr3:100723881
|
G | A | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.268+3823G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100723881 | ||||||
chr3:100723958
|
G | T | 2 | a0001c0001t0003g0014a0001c0001t0003g0081 | 4 | HG01123.hp2 HG01516.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.268+3900G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100723958 | ||||||
chr3:100723974
|
A | T | 1 | a0001c0003t0001g0052 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.268+3916A>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100723974 | ||||||
chr3:100724075
|
A | G | 24 | a0001c0001t0001g0142a0001c0002t0002g0003a0001c0002t0002g0021others(21): Show | 38 | HG00597.hp1 HG00639.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.268+4017A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100724075 | ||||||
chr3:100724264
|
G | A | 54 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(51): Show | 105 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.268+4206G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100724264 | ||||||
chr3:100724286
|
G | T | 1 | a0001c0001t0003g0091 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.268+4228G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100724286 | ||||||
chr3:100724309
|
ATTAG | A | 3 | a0001c0002t0002g0006a0001c0002t0002g0195a0001c0002t0002g0196 | 8 | NA18946.hp1 NA18947.hp2 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.268+4255_268+4258d others(6): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 100724309 | |||||
chr3:100724482
|
G | A | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.269-4230G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100724482 | ||||||
chr3:100724664
|
T | A | 1 | a0001c0002t0002g0169 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.269-4048T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100724664 | ||||||
chr3:100724755
|
A | G | 1 | a0001c0002t0002g0189 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.269-3957A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100724755 | ||||||
chr3:100724888
|
A | G | 13 | a0001c0003t0001g0027a0001c0003t0001g0048a0001c0003t0001g0049others(10): Show | 17 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.269-3824A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100724888 | ||||||
chr3:100725029
|
G | C | 3 | a0001c0001t0003g0007a0001c0001t0003g0145a0001c0001t0003g0146 | 7 | HG02258.hp2 HG02559.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.269-3683G>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100725029 | ||||||
chr3:100725060
|
C | T | 1 | a0001c0001t0003g0080 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.269-3652C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100725060 | ||||||
chr3:100725061
|
G | A | 7 | a0001c0003t0001g0027a0001c0003t0001g0048a0001c0003t0001g0049others(4): Show | 8 | HG01891.hp2 HG02615.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.269-3651G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100725061 | ||||||
chr3:100725098
|
G | T | 65 | a0001c0001t0003g0004a0001c0001t0003g0008a0001c0001t0003g0009others(62): Show | 87 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.269-3614G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100725098 | ||||||
chr3:100725186
|
A | G | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.269-3526A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100725186 | ||||||
chr3:100725286
|
A | G | 14 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0048others(11): Show | 19 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.269-3426A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100725286 | ||||||
chr3:100725326
|
A | T | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.269-3386A>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100725326 | ||||||
chr3:100725485
|
A | C | 1 | a0001c0003t0001g0044 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.269-3227A>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100725485 | ||||||
chr3:100725622
|
C | CA | 14 | a0001c0001t0003g0055a0001c0001t0003g0072a0001c0001t0003g0073others(11): Show | 18 | HG00735.hp2 HG01243.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.269-3067dupA | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 100725622 | |||||
chr3:100725622
|
CA | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(75): Show | 143 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.269-3067delA | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 100725622 | |||||
chr3:100725622
|
CAA | C | 5 | a0001c0001t0001g0018a0001c0001t0001g0126a0001c0001t0001g0127others(2): Show | 7 | HG01123.hp1 HG01256.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.269-3068_269-3067d others(4): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 100725622 | |||||
chr3:100725622
|
CAAAA | C | 6 | a0001c0004t0001g0012a0001c0004t0001g0026a0001c0004t0001g0045others(3): Show | 9 | HG00735.hp1 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.269-3070_269-3067d others(6): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 100725622 | |||||
chr3:100725622
|
CAAAAAA | C | 5 | a0001c0003t0001g0027a0001c0003t0001g0048a0001c0003t0001g0050others(2): Show | 6 | HG01891.hp2 HG02615.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-3072_269-3067d others(8): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 100725622 | |||||
chr3:100725672
|
G | T | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.269-3040G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100725672 | ||||||
chr3:100725676
|
T | TC | 143 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(140): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.269-3034dupC | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 100725676 | |||||
chr3:100725920
|
T | C | 1 | a0001c0003t0001g0044 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.269-2792T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100725920 | ||||||
chr3:100725923
|
G | A | 1 | a0001c0001t0004g0083 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.269-2789G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100725923 | ||||||
chr3:100725928
|
A | C | 1 | a0001c0001t0003g0069 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.269-2784A>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100725928 | ||||||
chr3:100726010
|
G | C | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.269-2702G>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100726010 | ||||||
chr3:100726118
|
G | A | 5 | a0001c0002t0002g0006a0001c0002t0002g0041a0001c0002t0002g0195others(2): Show | 11 | NA18946.hp1 NA18947.hp2 NA18957.hp1 others(8): Show |
intron_variant | MODIFIER | c.269-2594G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100726118 | ||||||
chr3:100726223
|
G | A | 2 | a0001c0002t0002g0164a0001c0002t0002g0170 | 2 | HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.269-2489G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100726223 | ||||||
chr3:100726311
|
G | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(140): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.269-2401G>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100726311 | ||||||
chr3:100726398
|
G | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(140): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.269-2314G>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100726398 | ||||||
chr3:100726411
|
AC | A | 25 | a0001c0002t0002g0003a0001c0002t0002g0021a0001c0002t0002g0039others(22): Show | 39 | HG00597.hp1 HG00639.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.269-2298delC | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 100726411 | |||||
chr3:100726466
|
C | A | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.269-2246C>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100726466 | ||||||
chr3:100726620
|
C | G | 1 | a0001c0001t0001g0125 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.269-2092C>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100726620 | ||||||
chr3:100726684
|
A | G | 28 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0022others(25): Show | 58 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.269-2028A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100726684 | ||||||
chr3:100726773
|
A | AT | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.269-1930dupT | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 100726773 | |||||
chr3:100726820
|
C | T | 2 | a0001c0001t0003g0007a0001c0001t0003g0145 | 6 | HG02258.hp2 HG02559.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-1892C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100726820 | ||||||
chr3:100726852
|
C | T | 7 | a0001c0003t0001g0027a0001c0003t0001g0048a0001c0003t0001g0049others(4): Show | 8 | HG01891.hp2 HG02615.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.269-1860C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100726852 | ||||||
chr3:100726944
|
A | G | 1 | a0001c0001t0001g0124 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.269-1768A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100726944 | ||||||
chr3:100727216
|
G | A | 1 | a0001c0002t0002g0181 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.269-1496G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100727216 | ||||||
chr3:100727340
|
C | G | 3 | a0001c0001t0001g0130a0001c0001t0001g0136a0001c0001t0003g0204 | 3 | HG01891.hp1 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.269-1372C>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100727340 | ||||||
chr3:100727542
|
C | T | 1 | a0001c0001t0003g0088 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.269-1170C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100727542 | ||||||
chr3:100727613
|
G | A | 1 | a0001c0001t0003g0146 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.269-1099G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100727613 | ||||||
chr3:100727804
|
T | A | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.269-908T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100727804 | ||||||
chr3:100728170
|
G | T | 1 | a0001c0001t0001g0125 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.269-542G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100728170 | ||||||
chr3:100728293
|
C | T | 2 | a0001c0001t0010g0059a0001c0003t0001g0025 | 3 | HG01928.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.269-419C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100728293 | ||||||
chr3:100728321
|
T | C | 73 | a0001c0001t0003g0004a0001c0001t0003g0007a0001c0001t0003g0008others(70): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.269-391T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100728321 | ||||||
chr3:100728348
|
C | T | 1 | a0001c0003t0001g0025 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.269-364C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100728348 | ||||||
chr3:100728364
|
ATATT | A | 64 | a0001c0001t0003g0004a0001c0001t0003g0008a0001c0001t0003g0009others(61): Show | 86 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.269-345_269-342del others(4): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 100728364 | |||||
chr3:100728424
|
A | G | 1 | a0001c0003t0001g0044 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.269-288A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100728424 | ||||||
chr3:100728449
|
C | T | 1 | a0001c0001t0003g0146 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.269-263C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100728449 | ||||||
chr3:100728474
|
C | G | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.269-238C>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100728474 | ||||||
chr3:100728526
|
C | CT | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.269-179dupT | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 100728526 | |||||
chr3:100728571
|
T | A | 5 | a0001c0001t0006g0015a0001c0001t0006g0106a0001c0001t0008g0104others(2): Show | 7 | HG00280.hp1 HG01975.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.269-141T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100728571 | ||||||
chr3:100728572
|
T | A | 180 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(177): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.269-140T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100728572 | ||||||
chr3:100728573
|
A | T | 7 | a0001c0003t0001g0027a0001c0003t0001g0048a0001c0003t0001g0049others(4): Show | 8 | HG01891.hp2 HG02615.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.269-139A>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100728573 | ||||||
chr3:100728602
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.269-110T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100728602 | ||||||
chr3:100728947
|
G | A | 2 | a0001c0001t0001g0099a0001c0001t0001g0108 | 2 | HG00741.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.415+89G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100728947 | ||||||
chr3:100729021
|
G | A | 2 | a0001c0001t0001g0035a0001c0001t0001g0133 | 3 | NA18971.hp1 NA19001.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.415+163G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100729021 | ||||||
chr3:100729088
|
G | A | 3 | a0001c0001t0003g0007a0001c0001t0003g0145a0001c0001t0003g0146 | 7 | HG02258.hp2 HG02559.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.415+230G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100729088 | ||||||
chr3:100729254
|
C | T | 2 | a0001c0001t0008g0104a0001c0001t0008g0105 | 2 | HG02257.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.415+396C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100729254 | ||||||
chr3:100729339
|
T | G | 168 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(165): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.415+481T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100729339 | ||||||
chr3:100729347
|
A | T | 7 | a0001c0003t0001g0027a0001c0003t0001g0048a0001c0003t0001g0049others(4): Show | 8 | HG01891.hp2 HG02615.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+489A>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100729347 | ||||||
chr3:100729555
|
T | G | 4 | a0001c0001t0001g0017a0001c0001t0001g0126a0001c0001t0001g0140others(1): Show | 6 | HG01928.hp2 HG01993.hp2 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.415+697T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100729555 | ||||||
chr3:100729582
|
CTTA | C | 87 | a0001c0001t0003g0004a0001c0001t0003g0007a0001c0001t0003g0008others(84): Show | 120 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.415+733_415+735del others(3): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 100729582 | |||||
chr3:100729644
|
C | G | 73 | a0001c0001t0003g0004a0001c0001t0003g0007a0001c0001t0003g0008others(70): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.415+786C>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100729644 | ||||||
chr3:100729653
|
T | C | 1 | a0001c0003t0001g0053 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.415+795T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100729653 | ||||||
chr3:100729853
|
A | G | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.415+995A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100729853 | ||||||
chr3:100729865
|
A | G | 55 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(52): Show | 106 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.415+1007A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100729865 | ||||||
chr3:100729920
|
G | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(140): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.415+1062G>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100729920 | ||||||
chr3:100729928
|
A | G | 6 | a0001c0003t0001g0027a0001c0003t0001g0048a0001c0003t0001g0049others(3): Show | 7 | HG01891.hp2 HG02615.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.415+1070A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100729928 | ||||||
chr3:100729971
|
C | T | 1 | a0001c0003t0001g0044 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.415+1113C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100729971 | ||||||
chr3:100730020
|
G | T | 1 | a0001c0001t0001g0138 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.415+1162G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100730020 | ||||||
chr3:100730181
|
G | A | 1 | a0001c0001t0003g0103 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.415+1323G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100730181 | ||||||
chr3:100730251
|
A | G | 1 | a0001c0002t0002g0172 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.415+1393A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100730251 | ||||||
chr3:100730285
|
A | C | 2 | a0001c0001t0001g0130a0001c0001t0001g0136 | 2 | HG01891.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.415+1427A>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100730285 | ||||||
chr3:100730480
|
A | G | 1 | a0001c0001t0004g0071 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.415+1622A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100730480 | ||||||
chr3:100730501
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.415+1643T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100730501 | ||||||
chr3:100730502
|
A | G | 1 | a0001c0001t0001g0122 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.415+1644A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100730502 | ||||||
chr3:100730657
|
C | T | 73 | a0001c0001t0003g0004a0001c0001t0003g0007a0001c0001t0003g0008others(70): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.415+1799C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100730657 | ||||||
chr3:100730662
|
CAAG | C | 6 | a0001c0004t0001g0012a0001c0004t0001g0026a0001c0004t0001g0045others(3): Show | 9 | HG00735.hp1 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.415+1807_415+1809d others(5): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 100730662 | |||||
chr3:100730819
|
T | C | 1 | a0001c0003t0001g0044 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.416-1689T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100730819 | ||||||
chr3:100730935
|
A | G | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.416-1573A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100730935 | ||||||
chr3:100731083
|
G | A | 1 | a0001c0001t0001g0115 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.416-1425G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100731083 | ||||||
chr3:100731138
|
T | C | 3 | a0001c0001t0003g0007a0001c0001t0003g0145a0001c0001t0003g0146 | 7 | HG02258.hp2 HG02559.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.416-1370T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100731138 | ||||||
chr3:100731205
|
G | T | 1 | a0001c0003t0001g0044 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.416-1303G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100731205 | ||||||
chr3:100731536
|
C | T | 1 | a0001c0003t0001g0050 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.416-972C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100731536 | ||||||
chr3:100731667
|
G | A | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.416-841G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100731667 | ||||||
chr3:100731800
|
G | A | 2 | a0001c0002t0002g0186a0001c0002t0002g0191 | 2 | HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.416-708G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100731800 | ||||||
chr3:100731875
|
C | T | 1 | a0001c0003t0001g0044 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.416-633C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100731875 | ||||||
chr3:100732112
|
C | T | 1 | a0001c0001t0003g0146 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.416-396C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100732112 | ||||||
chr3:100732155
|
C | T | 6 | a0001c0004t0001g0012a0001c0004t0001g0026a0001c0004t0001g0045others(3): Show | 9 | HG00735.hp1 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.416-353C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100732155 | ||||||
chr3:100732184
|
C | CA | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.416-317dupA | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 100732184 | |||||
chr3:100732327
|
T | A | 14 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0048others(11): Show | 19 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.416-181T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100732327 | ||||||
chr3:100732399
|
A | G | 1 | a0001c0001t0003g0065 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.416-109A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100732399 | ||||||
chr3:100732499
|
T | C | 1 | a0001c0001t0003g0204 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.416-9T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100732499 | ||||||
chr3:100732722
|
G | A | 13 | a0001c0003t0001g0027a0001c0003t0001g0048a0001c0003t0001g0049others(10): Show | 17 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.580+50G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100732722 | ||||||
chr3:100732924
|
G | A | 3 | a0001c0001t0003g0007a0001c0001t0003g0145a0001c0001t0003g0146 | 7 | HG02258.hp2 HG02559.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.580+252G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100732924 | ||||||
chr3:100732936
|
T | C | 62 | a0001c0001t0003g0004a0001c0001t0003g0008a0001c0001t0003g0013others(59): Show | 82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.580+264T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100732936 | ||||||
chr3:100732998
|
A | G | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.580+326A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100732998 | ||||||
chr3:100733161
|
T | G | 1 | a0001c0001t0003g0146 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.580+489T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100733161 | ||||||
chr3:100733613
|
C | G | 1 | a0001c0003t0001g0044 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.580+941C>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100733613 | ||||||
chr3:100733724
|
A | G | 1 | a0001c0003t0001g0044 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.580+1052A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100733724 | ||||||
chr3:100733729
|
T | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(52): Show | 106 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.580+1057T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100733729 | ||||||
chr3:100733730
|
A | C | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.580+1058A>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100733730 | ||||||
chr3:100733740
|
G | A | 1 | a0001c0001t0003g0103 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.580+1068G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100733740 | ||||||
chr3:100733770
|
A | G | 1 | a0001c0002t0002g0158 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.580+1098A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100733770 | ||||||
chr3:100733773
|
T | G | 1 | a0001c0003t0001g0025 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.580+1101T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100733773 | ||||||
chr3:100733800
|
C | G | 73 | a0001c0001t0003g0004a0001c0001t0003g0007a0001c0001t0003g0008others(70): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.580+1128C>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100733800 | ||||||
chr3:100733824
|
G | C | 73 | a0001c0001t0003g0004a0001c0001t0003g0007a0001c0001t0003g0008others(70): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.580+1152G>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100733824 | ||||||
chr3:100733965
|
T | C | 1 | a0001c0001t0009g0131 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.580+1293T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100733965 | ||||||
chr3:100734032
|
G | C | 14 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0048others(11): Show | 19 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.580+1360G>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100734032 | ||||||
chr3:100734066
|
C | CT | 4 | a0001c0001t0003g0007a0001c0001t0003g0145a0001c0002t0002g0153others(1): Show | 8 | HG02055.hp1 HG02258.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.580+1404dupT | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 100734066 | |||||
chr3:100734067
|
T | A | 62 | a0001c0001t0003g0004a0001c0001t0003g0008a0001c0001t0003g0013others(59): Show | 82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.580+1395T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100734067 | ||||||
chr3:100734129
|
A | G | 14 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0048others(11): Show | 19 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.580+1457A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100734129 | ||||||
chr3:100734177
|
T | TA | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.580+1505_580+1506i others(3): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100734177 | ||||||
chr3:100734253
|
A | G | 1 | a0001c0002t0002g0163 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.580+1581A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100734253 | ||||||
chr3:100734341
|
G | C | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.580+1669G>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100734341 | ||||||
chr3:100734347
|
T | C | 1 | a0001c0001t0003g0081 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.580+1675T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100734347 | ||||||
chr3:100734401
|
G | T | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.580+1729G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100734401 | ||||||
chr3:100734458
|
A | G | 1 | a0001c0001t0001g0121 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.580+1786A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100734458 | ||||||
chr3:100734564
|
C | A | 1 | a0001c0003t0001g0044 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.580+1892C>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100734564 | ||||||
chr3:100734641
|
G | A | 4 | a0001c0001t0003g0013a0001c0001t0003g0062a0001c0001t0003g0068others(1): Show | 6 | NA18943.hp2 NA18961.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.581-1935G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100734641 | ||||||
chr3:100734991
|
A | G | 1 | a0001c0001t0001g0147 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.581-1585A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100734991 | ||||||
chr3:100735007
|
G | T | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.581-1569G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100735007 | ||||||
chr3:100735015
|
T | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(140): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.581-1561T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100735015 | ||||||
chr3:100735022
|
T | G | 7 | a0001c0003t0001g0027a0001c0003t0001g0048a0001c0003t0001g0049others(4): Show | 8 | HG01891.hp2 HG02615.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.581-1554T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100735022 | ||||||
chr3:100735280
|
G | A | 3 | a0001c0001t0003g0007a0001c0001t0003g0145a0001c0001t0003g0146 | 7 | HG02258.hp2 HG02559.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.581-1296G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100735280 | ||||||
chr3:100735387
|
C | T | 1 | a0001c0003t0001g0025 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.581-1189C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100735387 | ||||||
chr3:100735434
|
A | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(51): Show | 105 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.581-1142A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100735434 | ||||||
chr3:100735494
|
C | G | 1 | a0001c0003t0001g0044 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.581-1082C>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100735494 | ||||||
chr3:100735541
|
T | C | 1 | a0001c0002t0002g0167 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.581-1035T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100735541 | ||||||
chr3:100735712
|
T | C | 7 | a0001c0003t0001g0027a0001c0003t0001g0048a0001c0003t0001g0049others(4): Show | 8 | HG01891.hp2 HG02615.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.581-864T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100735712 | ||||||
chr3:100735787
|
A | G | 3 | a0001c0001t0003g0007a0001c0001t0003g0145a0001c0001t0003g0146 | 7 | HG02258.hp2 HG02559.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.581-789A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100735787 | ||||||
chr3:100735887
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.581-689C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100735887 | ||||||
chr3:100735902
|
G | A | 2 | a0001c0001t0006g0015a0001c0001t0006g0106 | 4 | HG01975.hp2 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.581-674G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100735902 | ||||||
chr3:100736154
|
G | T | 1 | a0001c0003t0001g0025 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.581-422G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100736154 | ||||||
chr3:100736295
|
T | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(52): Show | 106 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.581-281T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100736295 | ||||||
chr3:100736512
|
C | T | 1 | a0001c0002t0002g0157 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.581-64C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100736512 | ||||||
chr3:100736765
|
TG | T | 55 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(52): Show | 106 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.721+50delG | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100736765 | ||||||
chr3:100736958
|
C | T | 13 | a0001c0003t0001g0027a0001c0003t0001g0048a0001c0003t0001g0049others(10): Show | 17 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.721+242C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100736958 | ||||||
chr3:100736985
|
G | C | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.721+269G>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100736985 | ||||||
chr3:100736986
|
A | G | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.721+270A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100736986 | ||||||
chr3:100737094
|
TA | T | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.721+384delA | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 100737094 | |||||
chr3:100737165
|
C | A | 1 | a0001c0002t0002g0189 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.721+449C>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100737165 | ||||||
chr3:100737218
|
G | A | 2 | a0001c0001t0003g0082a0001c0001t0003g0092 | 2 | HG01346.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.721+502G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100737218 | ||||||
chr3:100737250
|
A | G | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.721+534A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100737250 | ||||||
chr3:100737383
|
C | T | 1 | a0001c0001t0001g0115 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.721+667C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100737383 | ||||||
chr3:100737384
|
A | G | 1 | a0001c0001t0003g0068 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.721+668A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100737384 | ||||||
chr3:100737562
|
G | A | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.721+846G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100737562 | ||||||
chr3:100737669
|
C | T | 1 | a0001c0004t0001g0207 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.721+953C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100737669 | ||||||
chr3:100737735
|
A | G | 1 | a0001c0001t0003g0078 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.721+1019A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100737735 | ||||||
chr3:100737740
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.721+1024C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100737740 | ||||||
chr3:100737916
|
A | G | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.721+1200A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100737916 | ||||||
chr3:100737988
|
A | G | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.721+1272A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100737988 | ||||||
chr3:100738085
|
CA | C | 95 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(92): Show | 165 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.721+1382delA | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 100738085 | |||||
chr3:100738085
|
CAA | C | 72 | a0001c0001t0003g0004a0001c0001t0003g0007a0001c0001t0003g0008others(69): Show | 100 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.721+1381_721+1382d others(4): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 100738085 | |||||
chr3:100738124
|
C | T | 1 | a0001c0001t0003g0204 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.721+1408C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100738124 | ||||||
chr3:100738177
|
C | T | 1 | a0001c0001t0003g0146 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.721+1461C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100738177 | ||||||
chr3:100738355
|
G | C | 1 | a0001c0001t0001g0111 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.721+1639G>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100738355 | ||||||
chr3:100738556
|
A | G | 1 | a0001c0002t0002g0183 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.721+1840A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100738556 | ||||||
chr3:100738763
|
C | A | 1 | a0001c0001t0001g0134 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.721+2047C>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100738763 | ||||||
chr3:100738796
|
C | T | 1 | a0001c0001t0001g0115 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.721+2080C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100738796 | ||||||
chr3:100738889
|
C | T | 1 | a0001c0003t0001g0025 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.721+2173C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100738889 | ||||||
chr3:100738941
|
T | C | 1 | a0001c0003t0001g0044 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.721+2225T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100738941 | ||||||
chr3:100739053
|
G | T | 1 | a0001c0003t0001g0044 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.721+2337G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100739053 | ||||||
chr3:100739090
|
T | G | 1 | a0001c0002t0002g0154 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.721+2374T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100739090 | ||||||
chr3:100739169
|
C | T | 2 | a0001c0001t0006g0015a0001c0001t0006g0106 | 4 | HG01975.hp2 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.721+2453C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100739169 | ||||||
chr3:100739247
|
G | T | 1 | a0001c0003t0001g0044 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.721+2531G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100739247 | ||||||
chr3:100739259
|
T | A | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.721+2543T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100739259 | ||||||
chr3:100739294
|
C | T | 1 | a0001c0001t0001g0112 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.721+2578C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100739294 | ||||||
chr3:100739355
|
T | G | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.721+2639T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100739355 | ||||||
chr3:100739416
|
G | A | 78 | a0001c0001t0003g0004a0001c0001t0003g0007a0001c0001t0003g0008others(75): Show | 107 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.721+2700G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100739416 | ||||||
chr3:100739507
|
A | G | 1 | a0001c0003t0001g0044 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.721+2791A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100739507 | ||||||
chr3:100739786
|
A | G | 1 | a0001c0002t0002g0171 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.721+3070A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100739786 | ||||||
chr3:100739807
|
C | T | 8 | a0001c0003t0001g0025a0001c0003t0001g0044a0001c0004t0001g0012others(5): Show | 12 | HG00280.hp1 HG00735.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.721+3091C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100739807 | ||||||
chr3:100739914
|
A | G | 1 | a0001c0001t0009g0131 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.721+3198A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100739914 | ||||||
chr3:100739922
|
G | A | 1 | a0001c0001t0003g0092 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.721+3206G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100739922 | ||||||
chr3:100740058
|
C | G | 1 | a0001c0001t0001g0113 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.721+3342C>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100740058 | ||||||
chr3:100740061
|
T | C | 1 | a0001c0002t0002g0197 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.721+3345T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100740061 | ||||||
chr3:100740152
|
A | G | 64 | a0001c0001t0003g0004a0001c0001t0003g0008a0001c0001t0003g0009others(61): Show | 86 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.721+3436A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100740152 | ||||||
chr3:100740252
|
C | T | 6 | a0001c0003t0001g0025a0001c0004t0001g0012a0001c0004t0001g0026others(3): Show | 10 | HG00735.hp1 HG02109.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.721+3536C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100740252 | ||||||
chr3:100740385
|
C | T | 4 | a0001c0001t0003g0014a0001c0001t0003g0058a0001c0001t0003g0080others(1): Show | 6 | HG00735.hp2 HG01123.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.721+3669C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100740385 | ||||||
chr3:100740461
|
T | A | 1 | a0001c0003t0001g0044 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.721+3745T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100740461 | ||||||
chr3:100740531
|
C | T | 55 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(52): Show | 106 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.721+3815C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100740531 | ||||||
chr3:100740691
|
G | A | 2 | a0001c0001t0003g0009a0001c0001t0011g0009 | 4 | HG01106.hp1 HG02572.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.721+3975G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100740691 | ||||||
chr3:100740995
|
A | G | 6 | a0001c0003t0001g0027a0001c0003t0001g0048a0001c0003t0001g0049others(3): Show | 7 | HG01891.hp2 HG02615.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.722-3838A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100740995 | ||||||
chr3:100741122
|
T | G | 24 | a0001c0001t0001g0142a0001c0002t0002g0003a0001c0002t0002g0021others(21): Show | 38 | HG00597.hp1 HG00639.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.722-3711T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100741122 | ||||||
chr3:100741137
|
TTTTA | T | 14 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0048others(11): Show | 19 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.722-3695_722-3692d others(6): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100741137 | ||||||
chr3:100741196
|
G | T | 1 | a0001c0003t0001g0048 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.722-3637G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100741196 | ||||||
chr3:100741257
|
G | A | 1 | a0001c0003t0001g0025 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.722-3576G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100741257 | ||||||
chr3:100741426
|
T | C | 2 | a0001c0001t0003g0007a0001c0001t0003g0145 | 6 | HG02258.hp2 HG02559.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.722-3407T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100741426 | ||||||
chr3:100741513
|
T | A | 1 | a0001c0001t0004g0074 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.722-3320T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100741513 | ||||||
chr3:100741601
|
A | G | 1 | a0001c0001t0001g0135 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.722-3232A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100741601 | ||||||
chr3:100741759
|
T | G | 55 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(52): Show | 106 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.722-3074T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100741759 | ||||||
chr3:100741862
|
G | A | 1 | a0001c0002t0002g0153 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.722-2971G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100741862 | ||||||
chr3:100741922
|
C | T | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.722-2911C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100741922 | ||||||
chr3:100742076
|
A | G | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.722-2757A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100742076 | ||||||
chr3:100742155
|
G | T | 1 | a0001c0001t0003g0086 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.722-2678G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100742155 | ||||||
chr3:100742178
|
G | A | 2 | a0001c0001t0006g0015a0001c0001t0006g0106 | 4 | HG01975.hp2 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.722-2655G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100742178 | ||||||
chr3:100742262
|
T | C | 2 | a0001c0001t0008g0104a0001c0001t0008g0105 | 2 | HG02257.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.722-2571T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100742262 | ||||||
chr3:100742271
|
G | A | 1 | a0001c0002t0002g0155 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.722-2562G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100742271 | ||||||
chr3:100742273
|
A | G | 2 | a0001c0001t0006g0015a0001c0001t0006g0106 | 4 | HG01975.hp2 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.722-2560A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100742273 | ||||||
chr3:100742532
|
T | A | 1 | a0001c0001t0001g0116 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.722-2301T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100742532 | ||||||
chr3:100742598
|
T | A | 128 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(125): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.722-2235T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100742598 | ||||||
chr3:100742620
|
A | G | 1 | a0001c0003t0001g0025 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.722-2213A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100742620 | ||||||
chr3:100742693
|
T | C | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.722-2140T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100742693 | ||||||
chr3:100742789
|
CTG | C | 14 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0048others(11): Show | 19 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.722-2040_722-2039d others(4): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 100742789 | |||||
chr3:100742890
|
C | CA | 71 | a0001c0001t0003g0004a0001c0001t0003g0008a0001c0001t0003g0009others(68): Show | 95 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.722-1932dupA | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 100742890 | |||||
chr3:100742890
|
CA | C | 15 | a0001c0001t0001g0112a0001c0003t0001g0025a0001c0003t0001g0027others(12): Show | 20 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.722-1932delA | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 100742890 | |||||
chr3:100743040
|
GT | G | 2 | a0001c0002t0002g0020a0001c0002t0002g0166 | 4 | HG02257.hp1 HG02486.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.722-1791delT | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 100743040 | |||||
chr3:100743064
|
A | G | 4 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0147others(1): Show | 4 | NA18951.hp1 NA18997.hp1 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.722-1769A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100743064 | ||||||
chr3:100743249
|
C | T | 1 | a0001c0001t0001g0118 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.722-1584C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100743249 | ||||||
chr3:100743398
|
C | T | 2 | a0001c0001t0006g0015a0001c0001t0006g0106 | 4 | HG01975.hp2 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.722-1435C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100743398 | ||||||
chr3:100743418
|
C | T | 14 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0048others(11): Show | 19 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.722-1415C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100743418 | ||||||
chr3:100743657
|
C | G | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.722-1176C>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100743657 | ||||||
chr3:100743683
|
A | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(140): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.722-1150A>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100743683 | ||||||
chr3:100743694
|
G | A | 2 | a0001c0001t0008g0104a0001c0001t0008g0105 | 2 | HG02257.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.722-1139G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100743694 | ||||||
chr3:100743731
|
C | T | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.722-1102C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100743731 | ||||||
chr3:100743803
|
C | CTT | 14 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0048others(11): Show | 19 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.722-1020_722-1019d others(4): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 100743803 | |||||
chr3:100744029
|
A | G | 2 | a0001c0001t0008g0104a0001c0001t0008g0105 | 2 | HG02257.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.722-804A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100744029 | ||||||
chr3:100744036
|
T | G | 1 | a0001c0001t0003g0146 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.722-797T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100744036 | ||||||
chr3:100744043
|
G | GA | 7 | a0001c0003t0001g0027a0001c0003t0001g0048a0001c0003t0001g0049others(4): Show | 8 | HG01891.hp2 HG02615.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.722-786dupA | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 100744043 | |||||
chr3:100744141
|
A | G | 2 | a0001c0001t0003g0007a0001c0001t0003g0145 | 6 | HG02258.hp2 HG02559.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.722-692A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100744141 | ||||||
chr3:100744334
|
C | G | 1 | a0001c0002t0002g0188 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.722-499C>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100744334 | ||||||
chr3:100744424
|
A | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(52): Show | 106 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.722-409A>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100744424 | ||||||
chr3:100744514
|
A | G | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.722-319A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100744514 | ||||||
chr3:100744548
|
G | T | 2 | a0001c0004t0001g0045a0001c0004t0001g0046 | 2 | HG02486.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.722-285G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100744548 | ||||||
chr3:100744776
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.722-57C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100744776 | ||||||
chr3:100744806
|
C | CGT | 2 | a0001c0002t0002g0023a0001c0002t0002g0192 | 4 | HG02083.hp1 HG02135.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.722-27_722-26insGT | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100744806 | ||||||
chr3:100744807
|
T | G | 28 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0022others(25): Show | 58 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.722-26T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100744807 | ||||||
chr3:100744807
|
T | TTG | 2 | a0001c0001t0006g0015a0001c0001t0006g0106 | 4 | HG01975.hp2 HG02970.hp2 HG03098.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.722-8_722-7dupGT | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 100744807 | |||||
chr3:100744825
|
G | T | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
splice_region_variant&intron_variant | LOW | c.722-8G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100744825 | ||||||
chr3:100744990
|
T | C | 1 | a0001c0003t0001g0025 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.820+59T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100744990 | ||||||
chr3:100745012
|
TTGTAG | T | 14 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0048others(11): Show | 19 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.820+83_820+87delGT others(3): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 100745012 | |||||
chr3:100745031
|
T | C | 1 | a0001c0003t0001g0044 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.820+100T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100745031 | ||||||
chr3:100745036
|
A | T | 1 | a0001c0003t0001g0044 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.820+105A>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100745036 | ||||||
chr3:100745075
|
A | C | 1 | a0001c0002t0002g0187 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.820+144A>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100745075 | ||||||
chr3:100745140
|
T | C | 73 | a0001c0001t0003g0004a0001c0001t0003g0007a0001c0001t0003g0008others(70): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.820+209T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100745140 | ||||||
chr3:100745165
|
T | C | 1 | a0001c0003t0001g0044 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.820+234T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100745165 | ||||||
chr3:100745179
|
GTT | G | 73 | a0001c0001t0003g0004a0001c0001t0003g0007a0001c0001t0003g0008others(70): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.820+252_820+253del others(2): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 100745179 | |||||
chr3:100745390
|
T | A | 1 | a0001c0001t0001g0117 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.820+459T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100745390 | ||||||
chr3:100745609
|
T | G | 1 | a0001c0003t0001g0044 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.820+678T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100745609 | ||||||
chr3:100745694
|
A | T | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.820+763A>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100745694 | ||||||
chr3:100745710
|
A | G | 1 | a0001c0001t0005g0063 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.820+779A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100745710 | ||||||
chr3:100745721
|
T | C | 1 | a0001c0001t0003g0032 | 2 | HG00738.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.820+790T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100745721 | ||||||
chr3:100745878
|
G | T | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.820+947G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100745878 | ||||||
chr3:100745920
|
C | A | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.820+989C>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100745920 | ||||||
chr3:100746086
|
C | A | 14 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0048others(11): Show | 19 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.820+1155C>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100746086 | ||||||
chr3:100746391
|
A | G | 24 | a0001c0001t0003g0004a0001c0001t0003g0013a0001c0001t0003g0028others(21): Show | 39 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.820+1460A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100746391 | ||||||
chr3:100746432
|
C | T | 20 | a0001c0001t0003g0008a0001c0001t0003g0056a0001c0001t0003g0073others(17): Show | 22 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(19): Show |
intron_variant | MODIFIER | c.820+1501C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100746432 | ||||||
chr3:100746510
|
A | T | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.820+1579A>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100746510 | ||||||
chr3:100746618
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.821-1531T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100746618 | ||||||
chr3:100746618
|
TAC | T | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.821-1519_821-1518d others(4): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 100746618 | |||||
chr3:100746753
|
TA | T | 15 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0044others(12): Show | 20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.821-1387delA | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 100746753 | |||||
chr3:100746765
|
A | G | 128 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(125): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.821-1384A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100746765 | ||||||
chr3:100746917
|
G | A | 1 | a0001c0003t0001g0025 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.821-1232G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100746917 | ||||||
chr3:100746922
|
A | G | 2 | a0001c0001t0003g0073a0001c0001t0003g0076 | 2 | NA18969.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.821-1227A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100746922 | ||||||
chr3:100746984
|
C | T | 14 | a0001c0003t0001g0025a0001c0003t0001g0027a0001c0003t0001g0048others(11): Show | 19 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.821-1165C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100746984 | ||||||
chr3:100747134
|
G | C | 1 | a0001c0001t0001g0124 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.821-1015G>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100747134 | ||||||
chr3:100747342
|
CT | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(53): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.821-796delT | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 100747342 | |||||
chr3:100747499
|
T | A | 1 | a0001c0001t0004g0074 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.821-650T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100747499 | ||||||
chr3:100747577
|
A | C | 3 | a0001c0002t0002g0156a0001c0002t0002g0159a0001c0002t0002g0160 | 3 | HG01256.hp2 HG01258.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.821-572A>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100747577 | ||||||
chr3:100747685
|
T | C | 1 | a0001c0002t0002g0172 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.821-464T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100747685 | ||||||
chr3:100747727
|
A | C | 13 | a0001c0003t0001g0027a0001c0003t0001g0048a0001c0003t0001g0049others(10): Show | 17 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.821-422A>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100747727 | ||||||
chr3:100747864
|
A | G | 13 | a0001c0003t0001g0027a0001c0003t0001g0048a0001c0003t0001g0049others(10): Show | 17 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.821-285A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100747864 |