geneid | 10915 |
---|---|
ensemblid | ENSG00000113649.14 |
hgncid | 15630 |
symbol | TCERG1 |
name | transcription elongation regulator 1 |
refseq_nuc | NM_001382548.1 |
refseq_prot | NP_001369477.1 |
ensembl_nuc | ENST00000679501.2 |
ensembl_prot | ENSP00000505217.1 |
mane_status | MANE Select |
chr | chr5 |
start | 146447333 |
end | 146511961 |
strand | + |
ver | v1.2 |
region | chr5:146447333-146511961 |
region5000 | chr5:146442333-146516961 |
regionname0 | TCERG1_chr5_146447333_146511961 |
regionname5000 | TCERG1_chr5_146442333_146516961 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1115 | 298 | 76 | 49 | 131 | 8 | 32 | 107 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0002 | 0/0 | 1111 | 7 | 3 | 4 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0003 | 0/0 | 1109 | 5 | 1 | 1 | 1 | 2 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0004 | 0/0 | 1117 | 3 | 2 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0005 | 0/0 | 1113 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0006 | 0/0 | 1115 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0007 | 0/0 | 1115 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0008 | 0/0 | 1119 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 3348 | 263 | 59 | 41 | 129 | 7 | 26 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
c0002 | 0/0 | 3348 | 14 | 4 | 5 | 0 | 0 | 5 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
c0003 | 0/0 | 3348 | 10 | 10 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
c0004 | 1/0 | 3348 | 6 | 1 | 3 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
c0005 | 0/0 | 3336 | 4 | 0 | 4 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
c0006 | 0/0 | 3330 | 3 | 0 | 1 | 0 | 2 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
c0007 | 0/0 | 3336 | 2 | 2 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
c0008 | 0/0 | 3348 | 2 | 2 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
c0009 | 0/0 | 3348 | 2 | 2 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
c0010 | 0/0 | 3354 | 2 | 1 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
c0011 | 0/0 | 3342 | 2 | 2 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
c0012 | 0/0 | 3348 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
c0013 | 0/0 | 3330 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
c0014 | 0/0 | 3342 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
c0015 | 0/0 | 3348 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
c0016 | 0/0 | 3348 | 1 | 0 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
c0017 | 0/0 | 3360 | 1 | 0 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
c0018 | 0/0 | 3348 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
c0019 | 0/0 | 3330 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
c0020 | 0/0 | 3336 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
c0021 | 0/0 | 3354 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1341 | 161 | 45 | 26 | 67 | 6 | 17 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
t0002 | 0/1 | 1341 | 94 | 1 | 14 | 64 | 5 | 9 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
t0003 | 0/0 | 1341 | 21 | 10 | 6 | 0 | 0 | 5 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
t0004 | 1/0 | 1337 | 17 | 7 | 8 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
t0005 | 0/0 | 1338 | 10 | 9 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
t0006 | 0/0 | 1338 | 4 | 4 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
t0007 | 0/0 | 1338 | 3 | 3 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
t0008 | 0/0 | 1340 | 3 | 2 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
t0009 | 0/0 | 1341 | 2 | 2 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
t0010 | 0/0 | 1341 | 2 | 2 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
t0011 | 0/0 | 1341 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
t0012 | 0/0 | 1341 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
t0013 | 0/0 | 1341 | 1 | 0 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 9 | 1 | 2 | 3 | 0 | 3 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0002 | 0/1 | 8 | 0 | 2 | 5 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0003 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0005 | 0/0 | 4 | 2 | 1 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0006 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0009 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0012 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0019 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0021 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 3348 | 263 | 59 | 41 | 129 | 7 | 26 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0001c0002 | 0/0 | 3348 | 14 | 4 | 5 | 0 | 0 | 5 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0001c0003 | 0/0 | 3348 | 10 | 10 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0001c0004 | 1/0 | 3348 | 6 | 1 | 3 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0001c0008 | 0/0 | 3348 | 2 | 2 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0001c0015 | 0/0 | 3348 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0001c0016 | 0/0 | 3348 | 1 | 0 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0001c0018 | 0/0 | 3348 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0002c0005 | 0/0 | 3336 | 4 | 0 | 4 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0002c0007 | 0/0 | 3336 | 2 | 2 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0002c0020 | 0/0 | 3336 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0003c0006 | 0/0 | 3330 | 3 | 0 | 1 | 0 | 2 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0003c0013 | 0/0 | 3330 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0003c0019 | 0/0 | 3330 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0004c0010 | 0/0 | 3354 | 2 | 1 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0004c0021 | 0/0 | 3354 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0005c0011 | 0/0 | 3342 | 2 | 2 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0005c0014 | 0/0 | 3342 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0006c0009 | 0/0 | 3348 | 2 | 2 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0007c0012 | 0/0 | 3348 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0008c0017 | 0/0 | 3360 | 1 | 0 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4688 | 140 | 30 | 24 | 67 | 2 | 17 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0001c0001t0002 | 0/1 | 4688 | 90 | 1 | 14 | 61 | 4 | 9 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0001c0001t0003 | 0/0 | 4688 | 7 | 6 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0001c0001t0004 | 0/0 | 4684 | 2 | 2 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0001c0001t0005 | 0/0 | 4685 | 10 | 9 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0001c0001t0006 | 0/0 | 4685 | 4 | 4 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0001c0001t0007 | 0/0 | 4685 | 3 | 3 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0001c0001t0008 | 0/0 | 4687 | 3 | 2 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0001c0001t0010 | 0/0 | 4688 | 2 | 2 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0001c0001t0012 | 0/0 | 4688 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0001c0001t0013 | 0/0 | 4688 | 1 | 0 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0001c0002t0003 | 0/0 | 4688 | 14 | 4 | 5 | 0 | 0 | 5 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0001c0003t0001 | 0/0 | 4688 | 9 | 9 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0001c0003t0011 | 0/0 | 4688 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0001c0004t0004 | 1/0 | 4684 | 6 | 1 | 3 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0001c0008t0009 | 0/0 | 4688 | 2 | 2 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0001c0015t0002 | 0/0 | 4688 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0001c0016t0001 | 0/0 | 4688 | 1 | 0 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0001c0018t0002 | 0/0 | 4688 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0002c0005t0004 | 0/0 | 4672 | 4 | 0 | 4 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0002c0007t0001 | 0/0 | 4676 | 2 | 2 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0002c0020t0001 | 0/0 | 4676 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0003c0006t0001 | 0/0 | 4670 | 3 | 0 | 1 | 0 | 2 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0003c0013t0002 | 0/0 | 4670 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0003c0019t0001 | 0/0 | 4670 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0004c0010t0001 | 0/0 | 4694 | 2 | 1 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0004c0021t0001 | 0/0 | 4694 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0005c0011t0004 | 0/0 | 4678 | 2 | 2 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0005c0014t0004 | 0/0 | 4678 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0006c0009t0004 | 0/0 | 4684 | 2 | 2 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0007c0012t0001 | 0/0 | 4688 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
a0008c0017t0002 | 0/0 | 4700 | 1 | 0 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | copy fasta | chr5 | 146442333 | 146516961 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 9 | 1 | 2 | 3 | 0 | 3 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0019 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0002 | 0/1 | 8 | 0 | 2 | 5 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0003 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0006 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0012 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0005g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0005g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0005g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0005g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0005g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0005g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0005g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0005g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0006g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0006g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0006g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0007g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0007g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0008g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0008g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0008g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0010g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0010g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0012g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0001t0013g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0002t0003g0005 | 0/0 | 4 | 2 | 1 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0002t0003g0009 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0002t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0002t0003g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0002t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0002t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0002t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0002t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0002t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0003t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0003t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0003t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0003t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0003t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0003t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0003t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0003t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0003t0011g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0004t0004g0021 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0004t0004g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0004t0004g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0004t0004g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0004t0004g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0008t0009g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0008t0009g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0015t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0016t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0001c0018t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0002c0005t0004g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0002c0005t0004g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0002c0005t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0002c0005t0004g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0002c0007t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0002c0007t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0002c0020t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0003c0006t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0003c0006t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0003c0006t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0003c0013t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0003c0019t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0004c0010t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0004c0010t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0004c0021t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0005c0011t0004g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0005c0011t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0005c0014t0004g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0006c0009t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0006c0009t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0007c0012t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
a0008c0017t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0016 | t0001 | g0136 | EUR | GBR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG00099 | hp2 | a0008 | c0017 | t0002 | g0036 | EUR | GBR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0006 | EUR | GBR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG00140 | hp2 | a0001 | c0001 | t0013 | g0203 | EUR | GBR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | CHS | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | CHS | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG00733 | hp1 | a0002 | c0005 | t0004 | g0189 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG00733 | hp2 | a0003 | c0006 | t0001 | g0171 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0089 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01069 | hp1 | a0002 | c0005 | t0004 | g0193 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01071 | hp2 | a0002 | c0005 | t0004 | g0188 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0077 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01167 | hp1 | a0001 | c0001 | t0005 | g0199 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01256 | hp2 | a0001 | c0002 | t0003 | g0240 | AMR | CLM | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01261 | hp1 | a0001 | c0004 | t0004 | g0251 | AMR | CLM | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01261 | hp2 | a0001 | c0002 | t0003 | g0005 | AMR | CLM | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01346 | hp1 | a0001 | c0004 | t0004 | g0250 | AMR | CLM | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01358 | hp2 | a0001 | c0004 | t0004 | g0249 | AMR | CLM | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01361 | hp1 | a0002 | c0005 | t0004 | g0190 | AMR | CLM | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01361 | hp2 | a0001 | c0002 | t0003 | g0243 | AMR | CLM | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01496 | hp2 | a0005 | c0014 | t0004 | g0185 | AMR | CLM | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0145 | EUR | IBS | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0108 | EUR | IBS | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01516 | hp1 | a0003 | c0006 | t0001 | g0133 | EUR | IBS | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | IBS | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01517 | hp1 | a0003 | c0006 | t0001 | g0132 | EUR | IBS | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | IBS | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01884 | hp1 | a0001 | c0001 | t0005 | g0197 | AFR | ACB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0254 | AMR | PEL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01943 | hp1 | a0001 | c0001 | t0008 | g0272 | AMR | PEL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | PEL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01975 | hp1 | a0001 | c0002 | t0003 | g0244 | AMR | PEL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01981 | hp1 | a0001 | c0002 | t0003 | g0241 | AMR | PEL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG01981 | hp2 | a0007 | c0012 | t0001 | g0181 | AMR | PEL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | KHV | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02027 | hp2 | a0001 | c0015 | t0002 | g0103 | EAS | KHV | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | KHV | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | KHV | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02055 | hp1 | a0001 | c0008 | t0009 | g0238 | AFR | ACB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02074 | hp1 | a0001 | c0001 | t0012 | g0261 | EAS | KHV | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | KHV | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02145 | hp1 | a0001 | c0002 | t0003 | g0113 | AFR | ACB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0094 | AMR | PEL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02257 | hp2 | a0001 | c0001 | t0007 | g0252 | AFR | ACB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02258 | hp1 | a0001 | c0003 | t0011 | g0176 | AFR | ACB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0107 | AMR | PEL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02451 | hp1 | a0001 | c0003 | t0001 | g0184 | AFR | ACB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | KHV | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02572 | hp1 | a0001 | c0001 | t0006 | g0025 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02572 | hp2 | a0002 | c0007 | t0001 | g0164 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02615 | hp1 | a0001 | c0003 | t0001 | g0016 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02622 | hp1 | a0001 | c0001 | t0007 | g0020 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02630 | hp2 | a0001 | c0003 | t0001 | g0179 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02647 | hp1 | a0001 | c0001 | t0004 | g0234 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02647 | hp2 | a0004 | c0021 | t0001 | g0201 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02683 | hp2 | a0001 | c0002 | t0003 | g0009 | SAS | PJL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02717 | hp2 | a0001 | c0001 | t0005 | g0194 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0073 | SAS | PJL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02809 | hp1 | a0001 | c0001 | t0010 | g0027 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0204 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0206 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02818 | hp2 | a0001 | c0001 | t0010 | g0026 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02886 | hp1 | a0001 | c0001 | t0006 | g0022 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02886 | hp2 | a0001 | c0001 | t0005 | g0018 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02896 | hp1 | a0002 | c0007 | t0001 | g0157 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02896 | hp2 | a0005 | c0011 | t0004 | g0192 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02922 | hp1 | a0001 | c0008 | t0009 | g0239 | AFR | ESN | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02965 | hp1 | a0001 | c0003 | t0001 | g0172 | AFR | ESN | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02965 | hp2 | a0006 | c0009 | t0004 | g0186 | AFR | ESN | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0257 | AFR | ESN | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0256 | AFR | ESN | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02976 | hp2 | a0001 | c0003 | t0001 | g0174 | AFR | ESN | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0076 | SAS | PJL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03098 | hp1 | a0002 | c0020 | t0001 | g0173 | AFR | MSL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03098 | hp2 | a0001 | c0001 | t0006 | g0024 | AFR | MSL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03139 | hp1 | a0001 | c0001 | t0005 | g0195 | AFR | ESN | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03195 | hp2 | a0001 | c0003 | t0001 | g0178 | AFR | ESN | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03209 | hp1 | a0004 | c0010 | t0001 | g0236 | AFR | MSL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | MSL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03225 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | MSL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03453 | hp1 | a0001 | c0004 | t0004 | g0021 | AFR | MSL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03486 | hp1 | a0001 | c0001 | t0008 | g0028 | AFR | MSL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03486 | hp2 | a0001 | c0001 | t0008 | g0029 | AFR | MSL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0086 | SAS | PJL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03491 | hp2 | a0001 | c0002 | t0003 | g0245 | SAS | PJL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03492 | hp1 | a0001 | c0002 | t0003 | g0009 | SAS | PJL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03516 | hp2 | a0005 | c0011 | t0004 | g0191 | AFR | ESN | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03540 | hp2 | a0001 | c0003 | t0001 | g0016 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03579 | hp1 | a0001 | c0003 | t0001 | g0177 | AFR | MSL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03579 | hp2 | a0003 | c0019 | t0001 | g0235 | AFR | MSL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03669 | hp2 | a0001 | c0002 | t0003 | g0009 | SAS | PJL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0051 | SAS | PJL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0069 | SAS | BEB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | BEB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0111 | SAS | BEB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | STU | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG04199 | hp2 | a0001 | c0004 | t0004 | g0248 | SAS | STU | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0056 | SAS | STU | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | STU | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0105 | SAS | STU | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18522 | hp2 | a0006 | c0009 | t0004 | g0187 | AFR | YRI | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19000 | hp1 | a0003 | c0013 | t0002 | g0054 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19001 | hp1 | a0001 | c0018 | t0002 | g0070 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | LWK | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19030 | hp2 | a0001 | c0002 | t0003 | g0005 | AFR | LWK | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | LWK | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19043 | hp2 | a0001 | c0003 | t0001 | g0175 | AFR | LWK | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | YRI | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0205 | AFR | YRI | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA20129 | hp1 | a0001 | c0001 | t0005 | g0018 | AFR | ASW | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA20129 | hp2 | a0001 | c0001 | t0004 | g0112 | AFR | ASW | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0274 | EUR | TSI | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA20752 | hp2 | a0004 | c0010 | t0001 | g0147 | EUR | TSI | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA20905 | hp1 | a0001 | c0002 | t0003 | g0005 | SAS | GIH | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | GIH | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02486 | hp1 | a0001 | c0001 | t0005 | g0198 | AFR | ACB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02486 | hp2 | a0001 | c0001 | t0005 | g0196 | AFR | ACB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02559 | hp1 | a0001 | c0002 | t0003 | g0242 | AFR | ACB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG02559 | hp2 | a0001 | c0001 | t0006 | g0023 | AFR | ACB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03471 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | MSL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0255 | AFR | MSL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
HG06807 | hp2 | a0001 | c0002 | t0003 | g0005 | AFR | USA | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | USA | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
NA20300 | hp2 | a0001 | c0001 | t0007 | g0020 | AFR | USA | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0002 | REF | REF | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
homoSapiens_grch38 | hp1 | a0001 | c0004 | t0004 | g0021 | REF | REF | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:146457274
|
G | A | 1 | a0007 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.377G>A | p.Gly126Asp | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/23 | 394/4684 | 377/3348 | 126/1115 | chr5 | 146457274 | ||
chr5:146459051
|
AGCTCAGG others(11): Show |
A | 1 | a0003 | 1 | NA19000.hp1 | disruptive_inframe_deletion | MODERATE | c.621_638delTCAGGCTC others(10): Show |
p.Gln208_Ala213del | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/23 | 638/4684 | 621/3348 | 207/1115 | INFO_REALIGN_3_PRIME | chr5 | 146459051 | |
chr5:146459072
|
T | TCAGGCC | 1 | a0004 | 3 | HG02647.hp2 HG03209.hp1 NA20752.hp2 |
disruptive_inframe_insertion | MODERATE | c.660_665dupGGCCCA | p.Gln222_Ala223insAl others(4): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/23 | 683/4684 | 666/3348 | 222/1115 | INFO_REALIGN_3_PRIME | chr5 | 146459072 | |
chr5:146459072
|
T | TCAGGCCC others(5): Show |
1 | a0008 | 1 | HG00099.hp2 | disruptive_inframe_insertion | MODERATE | c.654_665dupGGCCCAGG others(4): Show |
p.Gln222_Ala223insAl others(10): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/23 | 683/4684 | 666/3348 | 222/1115 | INFO_REALIGN_3_PRIME | chr5 | 146459072 | |
chr5:146459072
|
TCAGGCC | T | 1 | a0005 | 3 | HG01496.hp2 HG02896.hp2 HG03516.hp2 |
disruptive_inframe_deletion | MODERATE | c.660_665delGGCCCA | p.Ala221_Gln222del | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/23 | 677/4684 | 660/3348 | 220/1115 | INFO_REALIGN_3_PRIME | chr5 | 146459072 | |
chr5:146459072
|
TCAGGCCC others(5): Show |
T | 1 | a0002 | 7 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(4): Show |
disruptive_inframe_deletion | MODERATE | c.654_665delGGCCCAGG others(4): Show |
p.Ala219_Gln222del | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/23 | 671/4684 | 654/3348 | 218/1115 | INFO_REALIGN_3_PRIME | chr5 | 146459072 | |
chr5:146459072
|
TCAGGCCC others(11): Show |
T | 1 | a0003 | 4 | HG00733.hp2 HG01516.hp1 HG01517.hp1 others(1): Show |
disruptive_inframe_deletion | MODERATE | c.648_665delGGCCCAGG others(10): Show |
p.Ala217_Gln222del | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/23 | 665/4684 | 648/3348 | 216/1115 | INFO_REALIGN_3_PRIME | chr5 | 146459072 | |
chr5:146459281
|
C | T | 1 | a0006 | 2 | HG02965.hp2 NA18522.hp2 |
missense_variant | MODERATE | c.836C>T | p.Pro279Leu | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/23 | 853/4684 | 836/3348 | 279/1115 | chr5 | 146459281 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:146447391
|
C | T | 4 | a0001c0003a0002c0020a0003c0019others(1): Show | 13 | HG02258.hp1 HG02451.hp1 HG02615.hp1 others(10): Show |
synonymous_variant | LOW | c.42C>T | p.Phe14Phe | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/23 | 59/4684 | 42/3348 | 14/1115 | chr5 | 146447391 | ||
chr5:146455062
|
C | T | 2 | a0002c0005a0005c0011 | 6 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(3): Show |
synonymous_variant | LOW | c.66C>T | p.Ala22Ala | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 2/23 | 83/4684 | 66/3348 | 22/1115 | chr5 | 146455062 | ||
chr5:146459048
|
A | G | 1 | a0001c0018 | 1 | NA19001.hp1 | synonymous_variant | LOW | c.603A>G | p.Ala201Ala | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/23 | 620/4684 | 603/3348 | 201/1115 | chr5 | 146459048 | ||
chr5:146463675
|
G | A | 1 | a0001c0015 | 1 | HG02027.hp2 | synonymous_variant | LOW | c.1017G>A | p.Thr339Thr | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/23 | 1034/4684 | 1017/3348 | 339/1115 | chr5 | 146463675 | ||
chr5:146492961
|
C | G | 1 | a0001c0008 | 2 | HG02055.hp1 HG02922.hp1 |
synonymous_variant | LOW | c.2205C>G | p.Arg735Arg | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/23 | 2222/4684 | 2205/3348 | 735/1115 | chr5 | 146492961 | ||
chr5:146503380
|
A | G | 1 | a0001c0016 | 1 | HG00099.hp1 | synonymous_variant | LOW | c.2439A>G | p.Lys813Lys | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 18/23 | 2456/4684 | 2439/3348 | 813/1115 | chr5 | 146503380 | ||
chr5:146507890
|
G | A | 1 | a0001c0002 | 14 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(11): Show |
synonymous_variant | LOW | c.2979G>A | p.Thr993Thr | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 21/23 | 2996/4684 | 2979/3348 | 993/1115 | chr5 | 146507890 | ||
chr5:146510465
|
A | G | 20 | a0001c0001a0001c0002a0001c0003others(17): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
synonymous_variant | LOW | c.3171A>G | p.Ser1057Ser | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 23/23 | 3188/4684 | 3171/3348 | 1057/1115 | chr5 | 146510465 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:146510665
|
G | A | 3 | a0001c0001t0003a0001c0002t0003a0001c0008t0009 | 23 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*23G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 23/23 | 23 | chr5 | 146510665 | |||||
chr5:146510714
|
A | G | 1 | a0001c0001t0013 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*72A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 23/23 | 72 | chr5 | 146510714 | |||||
chr5:146510892
|
C | T | 5 | a0001c0001t0002a0001c0015t0002a0001c0018t0002others(2): Show | 94 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*250C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 23/23 | 250 | chr5 | 146510892 | |||||
chr5:146511063
|
C | T | 1 | a0001c0001t0012 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*421C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 23/23 | 421 | chr5 | 146511063 | |||||
chr5:146511219
|
CTTG | C | 1 | a0001c0001t0006 | 4 | HG02559.hp2 HG02572.hp1 HG02886.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*583_*585delGTT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 23/23 | 583 | INFO_REALIGN_3_PRIME | chr5 | 146511219 | ||||
chr5:146511559
|
C | T | 24 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(21): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
3_prime_UTR_variant | MODIFIER | c.*917C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 23/23 | 917 | chr5 | 146511559 | |||||
chr5:146511569
|
A | AAAG | 24 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(21): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
3_prime_UTR_variant | MODIFIER | c.*928_*930dupAAG | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 23/23 | 931 | INFO_REALIGN_3_PRIME | chr5 | 146511569 | ||||
chr5:146511641
|
T | C | 1 | a0001c0001t0010 | 2 | HG02809.hp1 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*999T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 23/23 | 999 | chr5 | 146511641 | |||||
chr5:146511646
|
A | G | 1 | a0001c0003t0011 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1004A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 23/23 | 1004 | chr5 | 146511646 | |||||
chr5:146511862
|
T | G | 1 | a0001c0008t0009 | 2 | HG02055.hp1 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1220T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 23/23 | 1220 | chr5 | 146511862 | |||||
chr5:146511880
|
G | A | 1 | a0001c0001t0005 | 10 | HG01167.hp1 HG01884.hp1 HG02486.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1238G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 23/23 | 1238 | chr5 | 146511880 | |||||
chr5:146511884
|
T | TA | 25 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(22): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
3_prime_UTR_variant | MODIFIER | c.*1251dupA | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 23/23 | 1252 | INFO_REALIGN_3_PRIME | chr5 | 146511884 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:146447522
|
C | T | 19 | a0001c0001t0001g0010a0001c0001t0001g0258a0001c0001t0001g0259others(16): Show | 21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.59+114C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146447522 | ||||||
chr5:146447633
|
G | T | 4 | a0001c0001t0003g0254a0001c0001t0003g0255a0001c0001t0003g0256others(1): Show | 4 | HG01934.hp1 HG02970.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.59+225G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146447633 | ||||||
chr5:146447658
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.59+250C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146447658 | ||||||
chr5:146447730
|
G | T | 1 | a0001c0001t0007g0252 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.59+322G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146447730 | ||||||
chr5:146447818
|
T | C | 269 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(266): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.59+410T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146447818 | ||||||
chr5:146447983
|
T | C | 4 | a0001c0001t0006g0022a0001c0001t0006g0023a0001c0001t0006g0024others(1): Show | 4 | HG02559.hp2 HG02572.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.59+575T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146447983 | ||||||
chr5:146447996
|
C | G | 1 | a0001c0001t0002g0246 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.59+588C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146447996 | ||||||
chr5:146448048
|
C | G | 2 | a0001c0001t0001g0274a0001c0001t0001g0275 | 2 | HG02257.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.59+640C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146448048 | ||||||
chr5:146448122
|
CAGAGGGG others(7): Show |
C | 8 | a0001c0002t0003g0005a0001c0002t0003g0009a0001c0002t0003g0240others(5): Show | 13 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.59+715_59+728delAG others(12): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146448122 | ||||||
chr5:146448328
|
CT | C | 14 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(11): Show | 14 | HG00738.hp2 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.59+927delT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | 146448328 | |||||
chr5:146448506
|
C | T | 3 | a0001c0001t0003g0255a0001c0001t0003g0256a0001c0001t0003g0257 | 3 | HG02970.hp1 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.59+1098C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146448506 | ||||||
chr5:146448670
|
A | G | 2 | a0001c0008t0009g0238a0001c0008t0009g0239 | 2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.59+1262A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146448670 | ||||||
chr5:146448887
|
A | G | 1 | a0001c0001t0001g0237 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.59+1479A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146448887 | ||||||
chr5:146448971
|
A | G | 1 | a0004c0010t0001g0236 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.59+1563A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146448971 | ||||||
chr5:146449035
|
G | A | 84 | a0001c0001t0001g0013a0001c0001t0001g0039a0001c0001t0001g0041others(81): Show | 99 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.59+1627G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146449035 | ||||||
chr5:146449390
|
A | G | 1 | a0003c0019t0001g0235 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.59+1982A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146449390 | ||||||
chr5:146449576
|
C | T | 1 | a0001c0001t0004g0234 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.59+2168C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146449576 | ||||||
chr5:146449640
|
A | T | 7 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0229others(4): Show | 7 | NA18950.hp1 NA18960.hp2 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.59+2232A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146449640 | ||||||
chr5:146449711
|
G | A | 2 | a0001c0001t0010g0026a0001c0001t0010g0027 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.59+2303G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146449711 | ||||||
chr5:146449946
|
A | AT | 154 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(151): Show | 171 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(168): Show |
intron_variant | MODIFIER | c.59+2539dupT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | 146449946 | |||||
chr5:146450192
|
T | A | 1 | a0001c0001t0008g0028 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.59+2784T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146450192 | ||||||
chr5:146450310
|
T | C | 1 | a0001c0001t0004g0112 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.59+2902T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146450310 | ||||||
chr5:146450401
|
G | T | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.59+2993G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146450401 | ||||||
chr5:146450495
|
T | A | 19 | a0001c0001t0001g0010a0001c0001t0001g0258a0001c0001t0001g0259others(16): Show | 21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.59+3087T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146450495 | ||||||
chr5:146450563
|
G | A | 2 | a0001c0001t0010g0026a0001c0001t0010g0027 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.59+3155G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146450563 | ||||||
chr5:146450653
|
A | G | 1 | a0001c0001t0013g0203 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.59+3245A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146450653 | ||||||
chr5:146450712
|
C | T | 144 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(141): Show | 161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.59+3304C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146450712 | ||||||
chr5:146450798
|
T | C | 1 | a0001c0001t0001g0237 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.59+3390T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146450798 | ||||||
chr5:146451009
|
C | T | 2 | a0001c0001t0010g0026a0001c0001t0010g0027 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.59+3601C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146451009 | ||||||
chr5:146451094
|
A | G | 1 | a0001c0001t0001g0202 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.59+3686A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146451094 | ||||||
chr5:146451196
|
T | C | 18 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206others(15): Show | 23 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.59+3788T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146451196 | ||||||
chr5:146451201
|
A | G | 145 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(142): Show | 162 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(159): Show |
intron_variant | MODIFIER | c.59+3793A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146451201 | ||||||
chr5:146451308
|
G | A | 152 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(149): Show | 169 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(166): Show |
intron_variant | MODIFIER | c.60-3748G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146451308 | ||||||
chr5:146451319
|
C | CT | 140 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0030others(137): Show | 162 | HG00140.hp1 HG00621.hp1 HG00673.hp2 others(159): Show |
intron_variant | MODIFIER | c.60-3721dupT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | 146451319 | |||||
chr5:146451319
|
C | CTT | 22 | a0001c0001t0001g0010a0001c0001t0001g0259a0001c0001t0001g0260others(19): Show | 24 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(21): Show |
intron_variant | MODIFIER | c.60-3722_60-3721dup others(2): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | 146451319 | |||||
chr5:146451411
|
C | T | 144 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(141): Show | 161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.60-3645C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146451411 | ||||||
chr5:146451483
|
C | T | 1 | a0001c0001t0004g0234 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.60-3573C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146451483 | ||||||
chr5:146451618
|
G | A | 4 | a0001c0001t0006g0022a0001c0001t0006g0023a0001c0001t0006g0024others(1): Show | 4 | HG02559.hp2 HG02572.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.60-3438G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146451618 | ||||||
chr5:146451635
|
C | A | 9 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206others(6): Show | 9 | HG01934.hp1 HG02055.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.60-3421C>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146451635 | ||||||
chr5:146451692
|
A | C | 1 | a0001c0001t0002g0111 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.60-3364A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146451692 | ||||||
chr5:146451693
|
ATATACTT others(326): Show |
A | 1 | a0001c0001t0002g0111 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.60-3362_60-3030del | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146451693 | ||||||
chr5:146451736
|
T | A | 260 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(257): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.60-3320T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146451736 | ||||||
chr5:146451737
|
A | T | 260 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(257): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.60-3319A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146451737 | ||||||
chr5:146451738
|
T | A | 260 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(257): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.60-3318T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146451738 | ||||||
chr5:146451773
|
G | GT | 76 | a0001c0001t0001g0013a0001c0001t0001g0048a0001c0001t0001g0273others(73): Show | 91 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.60-3269dupT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | 146451773 | |||||
chr5:146451773
|
G | GTTTTTTT others(348): Show |
1 | a0001c0001t0002g0110 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.60-3269_60-3268ins others(355): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | 146451773 | |||||
chr5:146451790
|
T | A | 1 | a0001c0001t0001g0227 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.60-3266T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146451790 | ||||||
chr5:146451852
|
A | G | 19 | a0001c0001t0001g0010a0001c0001t0001g0258a0001c0001t0001g0259others(16): Show | 21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.60-3204A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146451852 | ||||||
chr5:146451856
|
C | T | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.60-3200C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146451856 | ||||||
chr5:146451927
|
A | G | 10 | a0001c0001t0007g0020a0001c0002t0003g0005a0001c0002t0003g0009others(7): Show | 16 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.60-3129A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146451927 | ||||||
chr5:146452029
|
C | T | 1 | a0001c0001t0002g0111 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.60-3027C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452029 | ||||||
chr5:146452033
|
C | A | 1 | a0001c0001t0002g0111 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.60-3023C>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452033 | ||||||
chr5:146452034
|
C | A | 1 | a0001c0001t0002g0111 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.60-3022C>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452034 | ||||||
chr5:146452035
|
A | G | 1 | a0001c0001t0007g0020 | 2 | HG02622.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.60-3021A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452035 | ||||||
chr5:146452036
|
C | T | 1 | a0001c0001t0002g0111 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.60-3020C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452036 | ||||||
chr5:146452039
|
C | G | 1 | a0001c0001t0002g0111 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.60-3017C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452039 | ||||||
chr5:146452040
|
T | A | 1 | a0001c0001t0002g0111 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.60-3016T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452040 | ||||||
chr5:146452041
|
G | C | 1 | a0001c0001t0003g0254 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.60-3015G>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452041 | ||||||
chr5:146452042
|
C | A | 1 | a0001c0001t0002g0111 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.60-3014C>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452042 | ||||||
chr5:146452047
|
C | A | 1 | a0001c0001t0002g0111 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.60-3009C>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452047 | ||||||
chr5:146452049
|
A | T | 1 | a0001c0001t0002g0111 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.60-3007A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452049 | ||||||
chr5:146452050
|
A | G | 1 | a0001c0001t0002g0111 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.60-3006A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452050 | ||||||
chr5:146452051
|
G | A | 1 | a0001c0001t0002g0111 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.60-3005G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452051 | ||||||
chr5:146452085
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.60-2971G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452085 | ||||||
chr5:146452090
|
A | C | 2 | a0001c0001t0010g0026a0001c0001t0010g0027 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.60-2966A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452090 | ||||||
chr5:146452145
|
G | T | 1 | a0001c0001t0007g0252 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.60-2911G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452145 | ||||||
chr5:146452180
|
G | A | 1 | a0001c0001t0008g0029 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.60-2876G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452180 | ||||||
chr5:146452302
|
G | GT | 123 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0031others(120): Show | 138 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(135): Show |
intron_variant | MODIFIER | c.60-2748dupT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | 146452302 | |||||
chr5:146452422
|
A | C | 19 | a0001c0001t0001g0010a0001c0001t0001g0258a0001c0001t0001g0259others(16): Show | 21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.60-2634A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452422 | ||||||
chr5:146452704
|
T | C | 145 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(142): Show | 162 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(159): Show |
intron_variant | MODIFIER | c.60-2352T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452704 | ||||||
chr5:146452810
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.60-2246T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452810 | ||||||
chr5:146452840
|
C | T | 1 | a0001c0001t0004g0112 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.60-2216C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452840 | ||||||
chr5:146452870
|
C | T | 145 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(142): Show | 162 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(159): Show |
intron_variant | MODIFIER | c.60-2186C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452870 | ||||||
chr5:146452964
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.60-2092A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452964 | ||||||
chr5:146453133
|
C | G | 1 | a0001c0001t0001g0200 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.60-1923C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146453133 | ||||||
chr5:146453308
|
A | G | 124 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0031others(121): Show | 139 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(136): Show |
intron_variant | MODIFIER | c.60-1748A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146453308 | ||||||
chr5:146453323
|
G | A | 86 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(83): Show | 105 | HG00099.hp1 HG00140.hp2 HG00621.hp2 others(102): Show |
intron_variant | MODIFIER | c.60-1733G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146453323 | ||||||
chr5:146453419
|
T | C | 1 | a0001c0001t0002g0045 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.60-1637T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146453419 | ||||||
chr5:146453442
|
G | C | 1 | a0001c0001t0001g0273 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.60-1614G>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146453442 | ||||||
chr5:146453483
|
G | T | 10 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206others(7): Show | 10 | HG01934.hp1 HG02055.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.60-1573G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146453483 | ||||||
chr5:146453536
|
A | C | 1 | a0001c0001t0002g0109 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.60-1520A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146453536 | ||||||
chr5:146453758
|
C | T | 8 | a0001c0001t0005g0017a0001c0001t0005g0018a0001c0001t0005g0194others(5): Show | 10 | HG01167.hp1 HG01884.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.60-1298C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146453758 | ||||||
chr5:146453772
|
TA | T | 7 | a0001c0001t0001g0233a0001c0001t0002g0108a0001c0001t0010g0026others(4): Show | 7 | HG01069.hp1 HG01515.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.60-1267delA | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | 146453772 | |||||
chr5:146453797
|
G | C | 2 | a0001c0001t0010g0026a0001c0001t0010g0027 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.60-1259G>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146453797 | ||||||
chr5:146453840
|
C | G | 1 | a0001c0001t0007g0252 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.60-1216C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146453840 | ||||||
chr5:146453864
|
C | T | 143 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(140): Show | 160 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.60-1192C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146453864 | ||||||
chr5:146453872
|
T | C | 2 | a0001c0001t0010g0026a0001c0001t0010g0027 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.60-1184T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146453872 | ||||||
chr5:146453890
|
C | T | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG02080.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.60-1166C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146453890 | ||||||
chr5:146453915
|
C | T | 1 | a0001c0001t0008g0272 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.60-1141C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146453915 | ||||||
chr5:146453924
|
G | A | 1 | a0001c0001t0004g0234 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.60-1132G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146453924 | ||||||
chr5:146453981
|
C | T | 1 | a0001c0001t0003g0254 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.60-1075C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146453981 | ||||||
chr5:146454037
|
CA | C | 110 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0041others(107): Show | 127 | HG00099.hp2 HG00140.hp1 HG00673.hp2 others(124): Show |
intron_variant | MODIFIER | c.60-995delA | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | 146454037 | |||||
chr5:146454037
|
CAA | C | 13 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(10): Show | 13 | HG00738.hp2 HG01891.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.60-996_60-995delAA | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | 146454037 | |||||
chr5:146454037
|
CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0001g0115a0001c0001t0001g0116 | 2 | HG00741.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.60-1004_60-995delA others(9): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | 146454037 | |||||
chr5:146454037
|
CAAAAAAA others(4): Show |
C | 84 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(81): Show | 103 | HG00099.hp1 HG00140.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.60-1005_60-995delA others(10): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | 146454037 | |||||
chr5:146454207
|
A | AAAAAG | 140 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(137): Show | 157 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(154): Show |
intron_variant | MODIFIER | c.60-835_60-831dupAG others(3): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | 146454207 | |||||
chr5:146454261
|
T | C | 1 | a0001c0001t0006g0022 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.60-795T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146454261 | ||||||
chr5:146454274
|
A | C | 85 | a0001c0001t0001g0013a0001c0001t0001g0039a0001c0001t0001g0041others(82): Show | 100 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.60-782A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146454274 | ||||||
chr5:146454416
|
T | C | 1 | a0001c0001t0001g0117 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.60-640T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146454416 | ||||||
chr5:146454474
|
C | CT | 19 | a0001c0001t0001g0010a0001c0001t0001g0258a0001c0001t0001g0259others(16): Show | 21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.60-579dupT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | 146454474 | |||||
chr5:146454569
|
G | GT | 21 | a0001c0001t0001g0010a0001c0001t0001g0222a0001c0001t0001g0223others(18): Show | 23 | HG01943.hp1 HG02015.hp2 HG02074.hp1 others(20): Show |
intron_variant | MODIFIER | c.60-476dupT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | 146454569 | |||||
chr5:146454590
|
G | T | 1 | a0001c0001t0002g0107 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.60-466G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146454590 | ||||||
chr5:146454641
|
A | G | 1 | a0001c0001t0007g0252 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.60-415A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146454641 | ||||||
chr5:146454693
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.60-363G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146454693 | ||||||
chr5:146454702
|
A | G | 2 | a0001c0001t0010g0026a0001c0001t0010g0027 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.60-354A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146454702 | ||||||
chr5:146454718
|
C | T | 1 | a0007c0012t0001g0181 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.60-338C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146454718 | ||||||
chr5:146454725
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.60-331A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146454725 | ||||||
chr5:146454736
|
T | TA | 3 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206 | 3 | HG02809.hp2 HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.60-319dupA | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | 146454736 | |||||
chr5:146454738
|
C | T | 2 | a0001c0001t0001g0220a0001c0001t0001g0221 | 2 | HG02083.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.60-318C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146454738 | ||||||
chr5:146454804
|
T | G | 162 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(159): Show | 184 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(181): Show |
intron_variant | MODIFIER | c.60-252T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146454804 | ||||||
chr5:146454919
|
G | A | 8 | a0001c0001t0005g0017a0001c0001t0005g0018a0001c0001t0005g0194others(5): Show | 10 | HG01167.hp1 HG01884.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.60-137G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146454919 | ||||||
chr5:146454953
|
T | G | 3 | a0001c0001t0001g0225a0001c0001t0001g0226a0004c0010t0001g0236 | 3 | HG02451.hp2 HG03209.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.60-103T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146454953 | ||||||
chr5:146454966
|
C | T | 143 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(140): Show | 160 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.60-90C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146454966 | ||||||
chr5:146455392
|
G | T | 1 | a0001c0001t0001g0271 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.285+111G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 2/22 | chr5 | 146455392 | ||||||
chr5:146455529
|
C | G | 2 | a0001c0001t0010g0026a0001c0001t0010g0027 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.285+248C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 2/22 | chr5 | 146455529 | ||||||
chr5:146455544
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.285+263G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 2/22 | chr5 | 146455544 | ||||||
chr5:146455546
|
G | C | 1 | a0001c0001t0002g0046 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.285+265G>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 2/22 | chr5 | 146455546 | ||||||
chr5:146455687
|
C | G | 2 | a0001c0001t0010g0026a0001c0001t0010g0027 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.285+406C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 2/22 | chr5 | 146455687 | ||||||
chr5:146455782
|
G | A | 3 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121 | 3 | NA18943.hp2 NA18994.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.285+501G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 2/22 | chr5 | 146455782 | ||||||
chr5:146455848
|
T | A | 2 | a0001c0001t0010g0026a0001c0001t0010g0027 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.285+567T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 2/22 | chr5 | 146455848 | ||||||
chr5:146455872
|
G | T | 3 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270 | 3 | HG02080.hp1 HG02132.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.285+591G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 2/22 | chr5 | 146455872 | ||||||
chr5:146456082
|
G | T | 8 | a0001c0001t0005g0017a0001c0001t0005g0018a0001c0001t0005g0194others(5): Show | 10 | HG01167.hp1 HG01884.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.285+801G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 2/22 | chr5 | 146456082 | ||||||
chr5:146456316
|
A | G | 1 | a0001c0001t0006g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.286-867A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 2/22 | chr5 | 146456316 | ||||||
chr5:146456461
|
G | A | 1 | a0001c0001t0001g0259 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.286-722G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 2/22 | chr5 | 146456461 | ||||||
chr5:146456468
|
T | C | 1 | a0001c0002t0003g0113 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.286-715T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 2/22 | chr5 | 146456468 | ||||||
chr5:146456849
|
T | C | 1 | a0003c0019t0001g0235 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.286-334T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 2/22 | chr5 | 146456849 | ||||||
chr5:146457031
|
G | T | 1 | a0001c0001t0001g0225 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.286-152G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 2/22 | chr5 | 146457031 | ||||||
chr5:146457099
|
A | T | 49 | a0001c0001t0001g0207a0001c0001t0002g0002a0001c0001t0002g0003others(46): Show | 59 | HG00621.hp1 HG00673.hp2 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.286-84A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 2/22 | chr5 | 146457099 | ||||||
chr5:146457116
|
T | C | 2 | a0001c0001t0002g0078a0001c0001t0002g0079 | 2 | HG02040.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.286-67T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 2/22 | chr5 | 146457116 | ||||||
chr5:146457171
|
G | A | 1 | a0001c0001t0007g0020 | 2 | HG02622.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.286-12G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 2/22 | chr5 | 146457171 | ||||||
chr5:146457471
|
G | C | 2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | HG01099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.438+136G>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146457471 | ||||||
chr5:146457606
|
C | T | 2 | a0001c0001t0010g0026a0001c0001t0010g0027 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.438+271C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146457606 | ||||||
chr5:146457622
|
G | A | 1 | a0001c0001t0002g0056 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.438+287G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146457622 | ||||||
chr5:146457630
|
C | T | 3 | a0001c0001t0003g0255a0001c0001t0003g0256a0001c0001t0003g0257 | 3 | HG02970.hp1 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.438+295C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146457630 | ||||||
chr5:146457664
|
C | T | 1 | a0001c0001t0005g0198 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.438+329C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146457664 | ||||||
chr5:146457759
|
T | G | 2 | a0001c0001t0002g0038a0001c0001t0002g0057 | 2 | NA18965.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.438+424T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146457759 | ||||||
chr5:146458011
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.438+676G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146458011 | ||||||
chr5:146458125
|
A | G | 85 | a0001c0001t0001g0013a0001c0001t0001g0039a0001c0001t0001g0041others(82): Show | 100 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.439-759A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146458125 | ||||||
chr5:146458169
|
T | C | 124 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0031others(121): Show | 139 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(136): Show |
intron_variant | MODIFIER | c.439-715T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146458169 | ||||||
chr5:146458197
|
A | G | 1 | a0001c0001t0007g0252 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.439-687A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146458197 | ||||||
chr5:146458269
|
C | T | 1 | a0001c0001t0004g0234 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.439-615C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146458269 | ||||||
chr5:146458321
|
C | T | 1 | a0004c0010t0001g0236 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.439-563C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146458321 | ||||||
chr5:146458467
|
C | T | 1 | a0001c0001t0007g0252 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.439-417C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146458467 | ||||||
chr5:146458494
|
A | G | 1 | a0001c0001t0007g0252 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.439-390A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146458494 | ||||||
chr5:146458512
|
A | G | 154 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(151): Show | 171 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(168): Show |
intron_variant | MODIFIER | c.439-372A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146458512 | ||||||
chr5:146458529
|
G | C | 2 | a0002c0005t0004g0188a0002c0005t0004g0193 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.439-355G>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146458529 | ||||||
chr5:146458538
|
T | A | 1 | a0001c0001t0001g0226 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.439-346T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146458538 | ||||||
chr5:146458604
|
C | T | 9 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206others(6): Show | 9 | HG01934.hp1 HG02055.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.439-280C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146458604 | ||||||
chr5:146458710
|
T | C | 144 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(141): Show | 161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.439-174T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146458710 | ||||||
chr5:146458738
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.439-146C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146458738 | ||||||
chr5:146458813
|
A | G | 2 | a0001c0001t0010g0026a0001c0001t0010g0027 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.439-71A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146458813 | ||||||
chr5:146458877
|
G | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(71): Show | 92 | HG00099.hp1 HG00140.hp2 HG00621.hp2 others(89): Show |
splice_region_variant&intron_variant | LOW | c.439-7G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146458877 | ||||||
chr5:146459347
|
A | T | 1 | a0003c0006t0001g0171 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.892+10A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146459347 | ||||||
chr5:146459352
|
G | A | 3 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0003g0204 | 3 | HG02809.hp2 NA18981.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.892+15G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146459352 | ||||||
chr5:146459518
|
G | T | 8 | a0001c0001t0005g0017a0001c0001t0005g0018a0001c0001t0005g0194others(5): Show | 10 | HG01167.hp1 HG01884.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.892+181G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146459518 | ||||||
chr5:146459600
|
C | T | 84 | a0001c0001t0001g0013a0001c0001t0001g0039a0001c0001t0001g0041others(81): Show | 99 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.892+263C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146459600 | ||||||
chr5:146459689
|
G | A | 19 | a0001c0001t0001g0010a0001c0001t0001g0258a0001c0001t0001g0259others(16): Show | 21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.892+352G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146459689 | ||||||
chr5:146459778
|
A | G | 1 | a0001c0001t0001g0271 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.892+441A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146459778 | ||||||
chr5:146459926
|
G | A | 1 | a0001c0001t0007g0252 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.892+589G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146459926 | ||||||
chr5:146459945
|
T | A | 1 | a0001c0001t0002g0080 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.892+608T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146459945 | ||||||
chr5:146459988
|
G | T | 1 | a0001c0001t0001g0170 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.892+651G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146459988 | ||||||
chr5:146460103
|
T | G | 1 | a0001c0001t0002g0081 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.892+766T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146460103 | ||||||
chr5:146460236
|
A | G | 10 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206others(7): Show | 10 | HG01934.hp1 HG02055.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.892+899A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146460236 | ||||||
chr5:146460318
|
G | A | 1 | a0001c0001t0005g0198 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.892+981G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146460318 | ||||||
chr5:146460334
|
T | C | 2 | a0001c0003t0001g0172a0002c0020t0001g0173 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.892+997T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146460334 | ||||||
chr5:146460424
|
T | C | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | HG02056.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.892+1087T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146460424 | ||||||
chr5:146460426
|
A | ATT | 87 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(84): Show | 106 | HG00099.hp1 HG00140.hp2 HG00621.hp2 others(103): Show |
intron_variant | MODIFIER | c.892+1095_892+1096d others(4): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr5 | 146460426 | |||||
chr5:146460450
|
T | G | 3 | a0001c0001t0003g0255a0001c0001t0003g0256a0001c0001t0003g0257 | 3 | HG02970.hp1 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.892+1113T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146460450 | ||||||
chr5:146460584
|
A | G | 19 | a0001c0001t0001g0010a0001c0001t0001g0258a0001c0001t0001g0259others(16): Show | 21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.892+1247A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146460584 | ||||||
chr5:146460603
|
G | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0117a0001c0001t0001g0124others(7): Show | 13 | HG00621.hp2 HG00673.hp1 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.892+1266G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146460603 | ||||||
chr5:146460611
|
G | C | 9 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206others(6): Show | 9 | HG01934.hp1 HG02055.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.892+1274G>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146460611 | ||||||
chr5:146460747
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.892+1410G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146460747 | ||||||
chr5:146460954
|
G | A | 87 | a0001c0001t0001g0013a0001c0001t0001g0039a0001c0001t0001g0041others(84): Show | 102 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.892+1617G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146460954 | ||||||
chr5:146461214
|
AAATAT | A | 9 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206others(6): Show | 9 | HG01934.hp1 HG02055.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.892+1884_892+1888d others(7): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr5 | 146461214 | |||||
chr5:146461265
|
T | G | 3 | a0005c0014t0004g0185a0006c0009t0004g0186a0006c0009t0004g0187 | 3 | HG01496.hp2 HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.892+1928T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146461265 | ||||||
chr5:146461315
|
T | C | 145 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(142): Show | 162 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(159): Show |
intron_variant | MODIFIER | c.892+1978T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146461315 | ||||||
chr5:146461537
|
C | T | 2 | a0006c0009t0004g0186a0006c0009t0004g0187 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.893-2014C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146461537 | ||||||
chr5:146461658
|
A | C | 1 | a0001c0001t0002g0169 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.893-1893A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146461658 | ||||||
chr5:146461671
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.893-1880A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146461671 | ||||||
chr5:146461897
|
C | T | 1 | a0001c0001t0005g0197 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.893-1654C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146461897 | ||||||
chr5:146461903
|
G | T | 240 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(237): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.893-1648G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146461903 | ||||||
chr5:146461959
|
T | A | 1 | a0001c0001t0001g0207 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.893-1592T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146461959 | ||||||
chr5:146462716
|
A | G | 2 | a0001c0001t0001g0221a0001c0001t0002g0106 | 2 | NA18993.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.893-835A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146462716 | ||||||
chr5:146462906
|
A | G | 26 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206others(23): Show | 33 | HG01167.hp1 HG01256.hp2 HG01261.hp2 others(30): Show |
intron_variant | MODIFIER | c.893-645A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146462906 | ||||||
chr5:146462922
|
T | A | 269 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(266): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.893-629T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146462922 | ||||||
chr5:146463121
|
T | G | 1 | a0001c0001t0001g0225 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.893-430T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146463121 | ||||||
chr5:146463870
|
C | T | 1 | a0001c0001t0002g0105 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1135+77C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146463870 | ||||||
chr5:146464017
|
A | G | 1 | a0001c0001t0002g0057 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1135+224A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146464017 | ||||||
chr5:146464065
|
A | G | 3 | a0001c0001t0002g0037a0001c0001t0002g0104a0001c0015t0002g0103 | 3 | HG02027.hp2 NA18942.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1135+272A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146464065 | ||||||
chr5:146464127
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1135+334C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146464127 | ||||||
chr5:146464226
|
G | A | 2 | a0001c0001t0002g0058a0001c0001t0002g0059 | 2 | NA18981.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1135+433G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146464226 | ||||||
chr5:146464269
|
A | G | 1 | a0001c0001t0004g0234 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1135+476A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146464269 | ||||||
chr5:146464300
|
G | A | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | NA19060.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1135+507G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146464300 | ||||||
chr5:146464391
|
T | C | 19 | a0001c0001t0001g0010a0001c0001t0001g0258a0001c0001t0001g0259others(16): Show | 21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.1135+598T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146464391 | ||||||
chr5:146464558
|
C | T | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG03654.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1135+765C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146464558 | ||||||
chr5:146464757
|
C | T | 1 | a0001c0001t0002g0055 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1135+964C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146464757 | ||||||
chr5:146464785
|
A | T | 1 | a0001c0001t0004g0234 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1135+992A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146464785 | ||||||
chr5:146464791
|
C | G | 143 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(140): Show | 160 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.1135+998C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146464791 | ||||||
chr5:146464812
|
T | A | 1 | a0001c0002t0003g0113 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1135+1019T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146464812 | ||||||
chr5:146464955
|
T | A | 1 | a0001c0001t0001g0202 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1135+1162T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146464955 | ||||||
chr5:146465038
|
A | G | 2 | a0001c0001t0010g0026a0001c0001t0010g0027 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1135+1245A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146465038 | ||||||
chr5:146465054
|
A | G | 5 | a0001c0001t0001g0013a0001c0001t0001g0039a0001c0001t0001g0041others(2): Show | 6 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1135+1261A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146465054 | ||||||
chr5:146465351
|
T | C | 64 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0014others(61): Show | 78 | HG00099.hp1 HG00140.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1135+1558T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146465351 | ||||||
chr5:146465737
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1135+1944A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146465737 | ||||||
chr5:146465760
|
G | T | 8 | a0001c0001t0005g0017a0001c0001t0005g0018a0001c0001t0005g0194others(5): Show | 10 | HG01167.hp1 HG01884.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1135+1967G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146465760 | ||||||
chr5:146465801
|
G | A | 1 | a0001c0001t0007g0020 | 2 | HG02622.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1135+2008G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146465801 | ||||||
chr5:146465884
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1135+2091C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146465884 | ||||||
chr5:146465888
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1135+2095C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146465888 | ||||||
chr5:146465961
|
A | G | 154 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(151): Show | 171 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(168): Show |
intron_variant | MODIFIER | c.1135+2168A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146465961 | ||||||
chr5:146466020
|
C | CA | 12 | a0001c0001t0001g0233a0001c0001t0001g0253a0001c0001t0002g0077others(9): Show | 13 | HG01099.hp2 HG01884.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1135+2245dupA | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 146466020 | |||||
chr5:146466020
|
C | CAA | 103 | a0001c0001t0001g0013a0001c0001t0001g0039a0001c0001t0001g0041others(100): Show | 118 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.1135+2244_1135+224 others(6): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 146466020 | |||||
chr5:146466020
|
C | CAAA | 9 | a0001c0001t0001g0048a0001c0001t0001g0232a0001c0001t0002g0057others(6): Show | 9 | HG02145.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1135+2243_1135+224 others(7): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 146466020 | |||||
chr5:146466020
|
CA | C | 8 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(5): Show | 8 | HG01167.hp1 HG01257.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1135+2245delA | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 146466020 | |||||
chr5:146466039
|
G | A | 2 | a0002c0005t0004g0189a0002c0005t0004g0190 | 2 | HG00733.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1135+2246G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146466039 | ||||||
chr5:146466332
|
G | A | 86 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(83): Show | 105 | HG00099.hp1 HG00140.hp2 HG00621.hp2 others(102): Show |
intron_variant | MODIFIER | c.1136-2009G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146466332 | ||||||
chr5:146466405
|
AG | A | 6 | a0002c0005t0004g0188a0002c0005t0004g0189a0002c0005t0004g0190others(3): Show | 6 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1136-1931delG | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 146466405 | |||||
chr5:146466445
|
G | A | 2 | a0001c0001t0002g0043a0001c0001t0002g0083 | 2 | NA19085.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1136-1896G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146466445 | ||||||
chr5:146466462
|
A | G | 1 | a0001c0001t0001g0200 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1136-1879A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146466462 | ||||||
chr5:146466549
|
A | G | 1 | a0001c0001t0001g0231 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1136-1792A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146466549 | ||||||
chr5:146466592
|
G | T | 1 | a0001c0008t0009g0239 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1136-1749G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146466592 | ||||||
chr5:146466597
|
C | T | 8 | a0001c0001t0001g0010a0001c0001t0001g0262a0001c0001t0001g0263others(5): Show | 10 | HG02074.hp1 NA18939.hp2 NA18940.hp1 others(7): Show |
intron_variant | MODIFIER | c.1136-1744C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146466597 | ||||||
chr5:146466726
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1136-1615T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146466726 | ||||||
chr5:146466806
|
A | G | 1 | a0001c0001t0002g0076 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1136-1535A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146466806 | ||||||
chr5:146466969
|
G | A | 143 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(140): Show | 160 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.1136-1372G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146466969 | ||||||
chr5:146467005
|
A | C | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1136-1336A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146467005 | ||||||
chr5:146467189
|
T | A | 1 | a0001c0001t0002g0076 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1136-1152T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146467189 | ||||||
chr5:146467373
|
A | G | 3 | a0001c0001t0005g0018a0001c0001t0005g0196a0001c0001t0005g0199 | 4 | HG01167.hp1 HG02486.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1136-968A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146467373 | ||||||
chr5:146467456
|
C | T | 121 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0031others(118): Show | 136 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(133): Show |
intron_variant | MODIFIER | c.1136-885C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146467456 | ||||||
chr5:146467465
|
G | C | 151 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(148): Show | 168 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(165): Show |
intron_variant | MODIFIER | c.1136-876G>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146467465 | ||||||
chr5:146467776
|
T | C | 1 | a0003c0019t0001g0235 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1136-565T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146467776 | ||||||
chr5:146468023
|
A | C | 1 | a0001c0001t0003g0255 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1136-318A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146468023 | ||||||
chr5:146468090
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1136-251T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146468090 | ||||||
chr5:146468840
|
T | C | 1 | a0001c0001t0006g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1198+437T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 6/22 | chr5 | 146468840 | ||||||
chr5:146468880
|
CT | C | 6 | a0001c0001t0003g0255a0001c0001t0003g0256a0001c0001t0003g0257others(3): Show | 6 | HG02486.hp1 HG02717.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1198+488delT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr5 | 146468880 | |||||
chr5:146469174
|
A | T | 23 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(20): Show | 23 | HG01257.hp2 HG01258.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.1199-370A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 6/22 | chr5 | 146469174 | ||||||
chr5:146469403
|
C | A | 1 | a0001c0001t0007g0252 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1199-141C>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 6/22 | chr5 | 146469403 | ||||||
chr5:146469863
|
A | G | 163 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(160): Show | 185 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(182): Show |
intron_variant | MODIFIER | c.1399+119A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 7/22 | chr5 | 146469863 | ||||||
chr5:146469965
|
T | A | 1 | a0001c0001t0002g0109 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1399+221T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 7/22 | chr5 | 146469965 | ||||||
chr5:146469966
|
G | A | 145 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(142): Show | 162 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(159): Show |
intron_variant | MODIFIER | c.1399+222G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 7/22 | chr5 | 146469966 | ||||||
chr5:146470326
|
C | G | 1 | a0001c0001t0004g0234 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1400-310C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 7/22 | chr5 | 146470326 | ||||||
chr5:146470506
|
A | ATAT | 145 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(142): Show | 162 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(159): Show |
intron_variant | MODIFIER | c.1400-129_1400-127d others(5): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr5 | 146470506 | |||||
chr5:146470765
|
T | C | 145 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(142): Show | 162 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(159): Show |
intron_variant | MODIFIER | c.1512+17T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 8/22 | chr5 | 146470765 | ||||||
chr5:146470896
|
G | GT | 86 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(83): Show | 105 | HG00099.hp1 HG00140.hp2 HG00621.hp2 others(102): Show |
intron_variant | MODIFIER | c.1512+154dupT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr5 | 146470896 | |||||
chr5:146471203
|
C | T | 1 | a0003c0013t0002g0054 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1513-285C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 8/22 | chr5 | 146471203 | ||||||
chr5:146471267
|
C | T | 18 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206others(15): Show | 23 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.1513-221C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 8/22 | chr5 | 146471267 | ||||||
chr5:146471600
|
A | AT | 10 | a0001c0001t0001g0129a0001c0001t0001g0153a0001c0001t0004g0112others(7): Show | 10 | HG01496.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1601+40dupT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146471600 | |||||
chr5:146471600
|
AT | A | 142 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(139): Show | 159 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(156): Show |
intron_variant | MODIFIER | c.1601+40delT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146471600 | |||||
chr5:146471621
|
C | T | 9 | a0001c0002t0003g0005a0001c0002t0003g0009a0001c0002t0003g0113others(6): Show | 14 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.1601+45C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146471621 | ||||||
chr5:146471747
|
C | T | 3 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206 | 3 | HG02809.hp2 HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1601+171C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146471747 | ||||||
chr5:146471750
|
C | T | 1 | a0001c0001t0010g0027 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1601+174C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146471750 | ||||||
chr5:146471839
|
C | T | 1 | a0001c0001t0001g0233 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1601+263C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146471839 | ||||||
chr5:146471843
|
C | T | 1 | a0001c0001t0002g0074 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1601+267C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146471843 | ||||||
chr5:146471887
|
G | A | 3 | a0001c0003t0001g0177a0001c0003t0001g0178a0001c0003t0001g0184 | 3 | HG02451.hp1 HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1601+311G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146471887 | ||||||
chr5:146471892
|
C | T | 2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | HG01099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1601+316C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146471892 | ||||||
chr5:146472170
|
A | G | 1 | a0001c0001t0002g0102 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1601+594A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146472170 | ||||||
chr5:146472181
|
C | T | 1 | a0001c0001t0002g0101 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1601+605C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146472181 | ||||||
chr5:146472216
|
T | C | 1 | a0001c0001t0002g0060 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1601+640T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146472216 | ||||||
chr5:146472334
|
C | T | 144 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(141): Show | 161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.1601+758C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146472334 | ||||||
chr5:146472374
|
T | C | 144 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(141): Show | 161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.1601+798T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146472374 | ||||||
chr5:146472387
|
T | G | 1 | a0001c0001t0002g0061 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1601+811T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146472387 | ||||||
chr5:146472467
|
G | A | 1 | a0001c0001t0008g0028 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1601+891G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146472467 | ||||||
chr5:146472536
|
C | T | 144 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(141): Show | 161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.1601+960C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146472536 | ||||||
chr5:146472537
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1601+961G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146472537 | ||||||
chr5:146472548
|
A | G | 4 | a0002c0005t0004g0188a0002c0005t0004g0189a0002c0005t0004g0190others(1): Show | 4 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1601+972A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146472548 | ||||||
chr5:146472560
|
G | A | 9 | a0001c0002t0003g0005a0001c0002t0003g0009a0001c0002t0003g0113others(6): Show | 14 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.1601+984G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146472560 | ||||||
chr5:146472701
|
T | TCGTGTGT others(13): Show |
1 | a0001c0001t0002g0049 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1601+1125_1601+112 others(24): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146472701 | ||||||
chr5:146472701
|
T | TGTGTGTG others(12): Show |
1 | a0001c0001t0002g0058 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1601+1125_1601+112 others(23): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146472701 | ||||||
chr5:146472701
|
T | TTG | 86 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(83): Show | 104 | HG00099.hp1 HG00140.hp2 HG00621.hp2 others(101): Show |
intron_variant | MODIFIER | c.1601+1151_1601+115 others(6): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146472701 | |||||
chr5:146472701
|
T | TTGTG | 11 | a0001c0001t0001g0007a0001c0001t0001g0131a0001c0001t0001g0154others(8): Show | 13 | HG00733.hp2 HG01516.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.1601+1149_1601+115 others(8): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146472701 | |||||
chr5:146472701
|
T | TTGTGTGT others(3): Show |
7 | a0001c0001t0001g0034a0001c0001t0008g0272a0001c0002t0003g0005others(4): Show | 12 | HG01261.hp2 HG01361.hp2 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.1601+1143_1601+115 others(14): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146472701 | |||||
chr5:146472701
|
T | TTGTGTGT others(5): Show |
6 | a0001c0001t0001g0035a0001c0001t0001g0217a0001c0001t0001g0218others(3): Show | 6 | HG01257.hp2 HG01258.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1601+1141_1601+115 others(16): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146472701 | |||||
chr5:146472701
|
T | TTGTGTGT others(7): Show |
28 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0031others(25): Show | 29 | HG00738.hp2 HG01358.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1601+1139_1601+115 others(18): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146472701 | |||||
chr5:146472701
|
T | TTGTGTGT others(9): Show |
10 | a0001c0001t0001g0048a0001c0001t0001g0220a0001c0001t0001g0226others(7): Show | 10 | HG01256.hp2 HG02083.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1601+1137_1601+115 others(20): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146472701 | |||||
chr5:146472701
|
T | TTGTGTGT others(11): Show |
11 | a0001c0001t0001g0010a0001c0001t0001g0039a0001c0001t0001g0041others(8): Show | 15 | HG00140.hp1 HG01167.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.1601+1135_1601+115 others(22): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146472701 | |||||
chr5:146472701
|
T | TTGTGTGT others(13): Show |
50 | a0001c0001t0001g0223a0001c0001t0001g0275a0001c0001t0002g0002others(47): Show | 61 | HG00099.hp2 HG00621.hp1 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.1601+1133_1601+115 others(24): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146472701 | |||||
chr5:146472701
|
T | TTGTGTGT others(15): Show |
21 | a0001c0001t0001g0042a0001c0001t0001g0260a0001c0001t0001g0267others(18): Show | 22 | HG00673.hp2 HG02015.hp1 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.1601+1131_1601+115 others(26): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146472701 | |||||
chr5:146472701
|
T | TTGTGTGT others(17): Show |
6 | a0001c0001t0001g0258a0001c0001t0001g0270a0001c0001t0001g0271others(3): Show | 6 | HG00735.hp1 HG01952.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.1601+1129_1601+115 others(28): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146472701 | |||||
chr5:146472701
|
T | TTGTGTGT others(19): Show |
4 | a0001c0001t0001g0259a0001c0001t0001g0268a0001c0001t0002g0110others(1): Show | 4 | HG02027.hp2 HG02132.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.1601+1127_1601+115 others(30): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146472701 | |||||
chr5:146472701
|
T | TTGTGTGT others(21): Show |
2 | a0001c0001t0010g0026a0001c0001t0010g0027 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1601+1152_1601+115 others(32): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146472701 | |||||
chr5:146472701
|
T | TTGTGTGT others(23): Show |
3 | a0001c0001t0001g0273a0001c0001t0002g0062a0001c0001t0002g0075 | 3 | NA18943.hp1 NA19057.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1601+1152_1601+115 others(34): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146472701 | |||||
chr5:146472727
|
G | GTGTGTGT others(20): Show |
1 | a0001c0001t0001g0269 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1601+1152_1601+115 others(31): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146472727 | |||||
chr5:146472728
|
T | TGTGTGTG others(16): Show |
1 | a0001c0001t0001g0222 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1601+1152_1601+115 others(27): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146472728 | ||||||
chr5:146472752
|
C | T | 123 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0031others(120): Show | 138 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(135): Show |
intron_variant | MODIFIER | c.1601+1176C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146472752 | ||||||
chr5:146472799
|
C | T | 1 | a0001c0004t0004g0251 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1601+1223C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146472799 | ||||||
chr5:146472842
|
T | G | 1 | a0001c0001t0007g0252 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1601+1266T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146472842 | ||||||
chr5:146473061
|
AGGAAG | A | 6 | a0002c0005t0004g0188a0002c0005t0004g0189a0002c0005t0004g0190others(3): Show | 6 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1601+1487_1601+149 others(9): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146473061 | |||||
chr5:146473069
|
A | G | 1 | a0001c0001t0007g0252 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1601+1493A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146473069 | ||||||
chr5:146473114
|
A | G | 8 | a0001c0001t0005g0017a0001c0001t0005g0018a0001c0001t0005g0194others(5): Show | 10 | HG01167.hp1 HG01884.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1601+1538A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146473114 | ||||||
chr5:146473137
|
G | T | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG01243.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1601+1561G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146473137 | ||||||
chr5:146473187
|
T | C | 1 | a0002c0007t0001g0157 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1601+1611T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146473187 | ||||||
chr5:146473351
|
T | C | 144 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(141): Show | 161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.1601+1775T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146473351 | ||||||
chr5:146473442
|
A | G | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1601+1866A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146473442 | ||||||
chr5:146473539
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1601+1963T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146473539 | ||||||
chr5:146473573
|
C | T | 19 | a0001c0001t0001g0010a0001c0001t0001g0258a0001c0001t0001g0259others(16): Show | 21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.1601+1997C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146473573 | ||||||
chr5:146473577
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1601+2001G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146473577 | ||||||
chr5:146473681
|
A | T | 2 | a0001c0001t0010g0026a0001c0001t0010g0027 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1601+2105A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146473681 | ||||||
chr5:146473683
|
G | A | 1 | a0001c0001t0004g0234 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1601+2107G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146473683 | ||||||
chr5:146473701
|
G | A | 1 | a0005c0011t0004g0191 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1601+2125G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146473701 | ||||||
chr5:146473866
|
G | A | 1 | a0001c0001t0002g0084 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1601+2290G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146473866 | ||||||
chr5:146473904
|
C | T | 1 | a0001c0003t0011g0176 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1601+2328C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146473904 | ||||||
chr5:146473918
|
A | G | 1 | a0001c0001t0005g0197 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1601+2342A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146473918 | ||||||
chr5:146473930
|
A | G | 18 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206others(15): Show | 23 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.1601+2354A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146473930 | ||||||
chr5:146473958
|
A | G | 87 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(84): Show | 106 | HG00099.hp1 HG00140.hp2 HG00621.hp2 others(103): Show |
intron_variant | MODIFIER | c.1601+2382A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146473958 | ||||||
chr5:146474020
|
TGGCTATA others(25): Show |
T | 144 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(141): Show | 161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.1601+2458_1601+248 others(36): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146474020 | |||||
chr5:146474035
|
T | C | 1 | a0002c0007t0001g0157 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1601+2459T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146474035 | ||||||
chr5:146474170
|
G | A | 1 | a0001c0001t0002g0058 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1601+2594G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146474170 | ||||||
chr5:146474378
|
T | C | 1 | a0001c0001t0002g0058 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1601+2802T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146474378 | ||||||
chr5:146474407
|
C | G | 144 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(141): Show | 161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.1601+2831C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146474407 | ||||||
chr5:146474419
|
A | G | 1 | a0001c0001t0003g0206 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1601+2843A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146474419 | ||||||
chr5:146474553
|
A | G | 144 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(141): Show | 161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.1601+2977A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146474553 | ||||||
chr5:146474609
|
A | G | 2 | a0001c0001t0010g0026a0001c0001t0010g0027 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1601+3033A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146474609 | ||||||
chr5:146474645
|
G | A | 1 | a0001c0001t0002g0058 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1601+3069G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146474645 | ||||||
chr5:146474646
|
A | G | 1 | a0001c0001t0002g0058 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1601+3070A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146474646 | ||||||
chr5:146474658
|
C | A | 1 | a0001c0001t0002g0056 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1601+3082C>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146474658 | ||||||
chr5:146474732
|
G | A | 3 | a0001c0002t0003g0005a0001c0002t0003g0242a0001c0002t0003g0243 | 6 | HG01261.hp2 HG01361.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1601+3156G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146474732 | ||||||
chr5:146474743
|
A | G | 1 | a0001c0004t0004g0251 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1601+3167A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146474743 | ||||||
chr5:146474868
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1601+3292A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146474868 | ||||||
chr5:146474983
|
T | A | 1 | a0001c0001t0001g0035 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1601+3407T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146474983 | ||||||
chr5:146475053
|
G | A | 144 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(141): Show | 161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.1602-3440G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146475053 | ||||||
chr5:146475074
|
A | G | 9 | a0001c0002t0003g0005a0001c0002t0003g0009a0001c0002t0003g0113others(6): Show | 14 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.1602-3419A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146475074 | ||||||
chr5:146475082
|
C | T | 2 | a0002c0007t0001g0157a0002c0007t0001g0164 | 2 | HG02572.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1602-3411C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146475082 | ||||||
chr5:146475342
|
G | C | 1 | a0001c0001t0002g0111 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1602-3151G>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146475342 | ||||||
chr5:146475440
|
T | C | 144 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(141): Show | 161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.1602-3053T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146475440 | ||||||
chr5:146475485
|
A | G | 1 | a0001c0001t0002g0058 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1602-3008A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146475485 | ||||||
chr5:146475494
|
T | C | 144 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(141): Show | 161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.1602-2999T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146475494 | ||||||
chr5:146475570
|
TGATTAAA others(10): Show |
T | 1 | a0001c0001t0001g0180 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1602-2905_1602-288 others(21): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146475570 | |||||
chr5:146475668
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1602-2825G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146475668 | ||||||
chr5:146475725
|
T | C | 248 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(245): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.1602-2768T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146475725 | ||||||
chr5:146475771
|
T | G | 144 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(141): Show | 161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.1602-2722T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146475771 | ||||||
chr5:146475781
|
G | C | 36 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(33): Show | 36 | HG00738.hp2 HG01257.hp2 HG01258.hp1 others(33): Show |
intron_variant | MODIFIER | c.1602-2712G>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146475781 | ||||||
chr5:146475919
|
A | G | 1 | a0001c0001t0001g0152 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1602-2574A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146475919 | ||||||
chr5:146476283
|
T | C | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1602-2210T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146476283 | ||||||
chr5:146476285
|
G | A | 19 | a0001c0001t0001g0010a0001c0001t0001g0258a0001c0001t0001g0259others(16): Show | 21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.1602-2208G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146476285 | ||||||
chr5:146476444
|
T | C | 1 | a0001c0001t0002g0109 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1602-2049T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146476444 | ||||||
chr5:146476552
|
T | TA | 12 | a0001c0001t0001g0153a0001c0003t0001g0016a0001c0003t0001g0172others(9): Show | 13 | HG02258.hp1 HG02451.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1602-1933dupA | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146476552 | |||||
chr5:146476685
|
A | G | 8 | a0001c0001t0005g0017a0001c0001t0005g0018a0001c0001t0005g0194others(5): Show | 10 | HG01167.hp1 HG01884.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1602-1808A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146476685 | ||||||
chr5:146476739
|
G | A | 123 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0031others(120): Show | 138 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(135): Show |
intron_variant | MODIFIER | c.1602-1754G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146476739 | ||||||
chr5:146476760
|
C | T | 144 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(141): Show | 161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.1602-1733C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146476760 | ||||||
chr5:146476912
|
C | T | 1 | a0001c0001t0001g0265 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1602-1581C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146476912 | ||||||
chr5:146476997
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1602-1496C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146476997 | ||||||
chr5:146477034
|
T | C | 270 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(267): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.1602-1459T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146477034 | ||||||
chr5:146477090
|
G | A | 1 | a0001c0001t0004g0234 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1602-1403G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146477090 | ||||||
chr5:146477436
|
A | G | 3 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0247 | 3 | NA19002.hp1 NA19074.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1602-1057A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146477436 | ||||||
chr5:146477443
|
A | G | 1 | a0001c0001t0001g0224 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1602-1050A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146477443 | ||||||
chr5:146477464
|
C | T | 1 | a0001c0001t0003g0255 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1602-1029C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146477464 | ||||||
chr5:146477557
|
A | G | 3 | a0001c0001t0005g0018a0001c0001t0005g0196a0001c0001t0005g0199 | 4 | HG01167.hp1 HG02486.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1602-936A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146477557 | ||||||
chr5:146477586
|
GT | G | 144 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(141): Show | 161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.1602-897delT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146477586 | |||||
chr5:146477603
|
A | C | 79 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0006others(76): Show | 93 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.1602-890A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146477603 | ||||||
chr5:146477692
|
C | CT | 120 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0035others(117): Show | 142 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(139): Show |
intron_variant | MODIFIER | c.1602-778dupT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146477692 | |||||
chr5:146477692
|
C | CTT | 32 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(29): Show | 32 | HG00738.hp2 HG01175.hp2 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.1602-779_1602-778d others(4): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146477692 | |||||
chr5:146477692
|
CT | C | 6 | a0001c0001t0001g0119a0001c0001t0001g0135a0001c0001t0001g0168others(3): Show | 7 | HG02258.hp1 HG02622.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1602-778delT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146477692 | |||||
chr5:146477718
|
G | A | 1 | a0001c0001t0002g0089 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1602-775G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146477718 | ||||||
chr5:146477734
|
A | T | 11 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(8): Show | 11 | HG00738.hp2 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1602-759A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146477734 | ||||||
chr5:146477840
|
C | T | 1 | a0001c0001t0007g0252 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1602-653C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146477840 | ||||||
chr5:146477992
|
C | T | 84 | a0001c0001t0001g0013a0001c0001t0001g0039a0001c0001t0001g0041others(81): Show | 99 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.1602-501C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146477992 | ||||||
chr5:146478069
|
A | G | 3 | a0001c0001t0003g0255a0001c0001t0003g0256a0001c0001t0003g0257 | 3 | HG02970.hp1 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1602-424A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146478069 | ||||||
chr5:146478239
|
G | A | 2 | a0001c0001t0002g0069a0001c0001t0002g0076 | 2 | HG03017.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1602-254G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146478239 | ||||||
chr5:146478241
|
A | T | 19 | a0001c0001t0001g0010a0001c0001t0001g0258a0001c0001t0001g0259others(16): Show | 21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.1602-252A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146478241 | ||||||
chr5:146478388
|
G | A | 1 | a0004c0010t0001g0236 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1602-105G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146478388 | ||||||
chr5:146478447
|
A | G | 5 | a0001c0001t0001g0114a0001c0001t0001g0149a0001c0001t0001g0150others(2): Show | 5 | HG01069.hp2 HG01257.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.1602-46A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146478447 | ||||||
chr5:146478481
|
A | G | 2 | a0001c0001t0010g0026a0001c0001t0010g0027 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1602-12A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146478481 | ||||||
chr5:146478809
|
G | C | 1 | a0001c0001t0007g0252 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1762+156G>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 10/22 | chr5 | 146478809 | ||||||
chr5:146478862
|
G | T | 9 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206others(6): Show | 9 | HG01934.hp1 HG02055.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1762+209G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 10/22 | chr5 | 146478862 | ||||||
chr5:146478917
|
G | A | 19 | a0001c0001t0001g0010a0001c0001t0001g0258a0001c0001t0001g0259others(16): Show | 21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.1762+264G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 10/22 | chr5 | 146478917 | ||||||
chr5:146478967
|
G | A | 153 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(150): Show | 170 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(167): Show |
intron_variant | MODIFIER | c.1762+314G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 10/22 | chr5 | 146478967 | ||||||
chr5:146479225
|
G | A | 1 | a0001c0001t0007g0020 | 2 | HG02622.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1762+572G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 10/22 | chr5 | 146479225 | ||||||
chr5:146479257
|
G | T | 1 | a0001c0001t0003g0206 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1763-598G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 10/22 | chr5 | 146479257 | ||||||
chr5:146479328
|
TTA | T | 9 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206others(6): Show | 9 | HG01934.hp1 HG02055.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1763-524_1763-523d others(4): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr5 | 146479328 | |||||
chr5:146479387
|
A | T | 1 | a0001c0002t0003g0113 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1763-468A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 10/22 | chr5 | 146479387 | ||||||
chr5:146479423
|
C | G | 1 | a0001c0001t0001g0273 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1763-432C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 10/22 | chr5 | 146479423 | ||||||
chr5:146479453
|
T | C | 2 | a0001c0001t0002g0003a0001c0001t0002g0108 | 5 | HG01256.hp1 HG01258.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.1763-402T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 10/22 | chr5 | 146479453 | ||||||
chr5:146479456
|
G | T | 2 | a0001c0001t0002g0003a0001c0001t0002g0108 | 5 | HG01256.hp1 HG01258.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.1763-399G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 10/22 | chr5 | 146479456 | ||||||
chr5:146479477
|
A | G | 1 | a0001c0002t0003g0113 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1763-378A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 10/22 | chr5 | 146479477 | ||||||
chr5:146479528
|
G | A | 1 | a0001c0001t0003g0204 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1763-327G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 10/22 | chr5 | 146479528 | ||||||
chr5:146479655
|
A | C | 84 | a0001c0001t0001g0013a0001c0001t0001g0039a0001c0001t0001g0041others(81): Show | 99 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.1763-200A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 10/22 | chr5 | 146479655 | ||||||
chr5:146480200
|
G | A | 143 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(140): Show | 160 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.1886+106G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | chr5 | 146480200 | ||||||
chr5:146480226
|
A | G | 144 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(141): Show | 161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.1886+132A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | chr5 | 146480226 | ||||||
chr5:146480309
|
T | G | 2 | a0001c0001t0010g0026a0001c0001t0010g0027 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1886+215T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | chr5 | 146480309 | ||||||
chr5:146480414
|
C | A | 2 | a0001c0008t0009g0238a0001c0008t0009g0239 | 2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1886+320C>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | chr5 | 146480414 | ||||||
chr5:146480532
|
C | T | 1 | a0001c0001t0002g0097 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1886+438C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | chr5 | 146480532 | ||||||
chr5:146480549
|
G | T | 1 | a0001c0001t0001g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1886+455G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | chr5 | 146480549 | ||||||
chr5:146480559
|
C | G | 1 | a0003c0019t0001g0235 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1886+465C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | chr5 | 146480559 | ||||||
chr5:146480573
|
A | T | 1 | a0001c0001t0001g0148 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1886+479A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | chr5 | 146480573 | ||||||
chr5:146480584
|
T | C | 144 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(141): Show | 161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.1886+490T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | chr5 | 146480584 | ||||||
chr5:146480617
|
T | A | 1 | a0001c0001t0004g0112 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1886+523T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | chr5 | 146480617 | ||||||
chr5:146480627
|
G | T | 1 | a0001c0001t0003g0254 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1887-523G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | chr5 | 146480627 | ||||||
chr5:146480630
|
G | A | 123 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0031others(120): Show | 138 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(135): Show |
intron_variant | MODIFIER | c.1887-520G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | chr5 | 146480630 | ||||||
chr5:146480710
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1887-440A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | chr5 | 146480710 | ||||||
chr5:146480837
|
A | G | 1 | a0001c0001t0002g0104 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1887-313A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | chr5 | 146480837 | ||||||
chr5:146480880
|
G | A | 79 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0006others(76): Show | 93 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.1887-270G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | chr5 | 146480880 | ||||||
chr5:146480925
|
A | G | 1 | a0001c0001t0002g0053 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1887-225A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | chr5 | 146480925 | ||||||
chr5:146480967
|
C | T | 1 | a0001c0001t0002g0071 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1887-183C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | chr5 | 146480967 | ||||||
chr5:146480967
|
CT | C | 24 | a0001c0001t0001g0125a0001c0001t0001g0146a0001c0001t0002g0099others(21): Show | 29 | HG01069.hp1 HG01256.hp2 HG01261.hp2 others(26): Show |
intron_variant | MODIFIER | c.1887-174delT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr5 | 146480967 | |||||
chr5:146480975
|
T | A | 2 | a0001c0001t0002g0058a0001c0001t0007g0020 | 3 | HG02622.hp1 NA18981.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1887-175T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | chr5 | 146480975 | ||||||
chr5:146480975
|
T | TA | 3 | a0001c0001t0010g0026a0001c0001t0010g0027a0001c0001t0012g0261 | 3 | HG02074.hp1 HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1887-175_1887-174i others(3): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | chr5 | 146480975 | ||||||
chr5:146480976
|
T | A | 244 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(241): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.1887-174T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | chr5 | 146480976 | ||||||
chr5:146481356
|
C | CT | 18 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206others(15): Show | 23 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.1937+157dupT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr5 | 146481356 | |||||
chr5:146481868
|
C | G | 1 | a0001c0001t0002g0074 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1937+668C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 13/22 | chr5 | 146481868 | ||||||
chr5:146482126
|
T | C | 1 | a0001c0001t0002g0050 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1938-466T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 13/22 | chr5 | 146482126 | ||||||
chr5:146482174
|
A | G | 2 | a0002c0007t0001g0157a0002c0007t0001g0164 | 2 | HG02572.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1938-418A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 13/22 | chr5 | 146482174 | ||||||
chr5:146482281
|
CT | C | 85 | a0001c0001t0001g0013a0001c0001t0001g0039a0001c0001t0001g0041others(82): Show | 100 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.1938-299delT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr5 | 146482281 | |||||
chr5:146482293
|
T | A | 3 | a0005c0014t0004g0185a0006c0009t0004g0186a0006c0009t0004g0187 | 3 | HG01496.hp2 HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1938-299T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 13/22 | chr5 | 146482293 | ||||||
chr5:146482304
|
G | T | 1 | a0001c0001t0001g0259 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1938-288G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 13/22 | chr5 | 146482304 | ||||||
chr5:146482346
|
C | T | 84 | a0001c0001t0001g0013a0001c0001t0001g0039a0001c0001t0001g0041others(81): Show | 99 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.1938-246C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 13/22 | chr5 | 146482346 | ||||||
chr5:146482377
|
T | A | 123 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0031others(120): Show | 138 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(135): Show |
intron_variant | MODIFIER | c.1938-215T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 13/22 | chr5 | 146482377 | ||||||
chr5:146482420
|
A | G | 1 | a0001c0001t0005g0196 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1938-172A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 13/22 | chr5 | 146482420 | ||||||
chr5:146482900
|
A | G | 144 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(141): Show | 161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.2073+173A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 14/22 | chr5 | 146482900 | ||||||
chr5:146483116
|
C | T | 1 | a0001c0001t0007g0020 | 2 | HG02622.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2073+389C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 14/22 | chr5 | 146483116 | ||||||
chr5:146483117
|
A | C | 1 | a0001c0001t0007g0020 | 2 | HG02622.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2073+390A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 14/22 | chr5 | 146483117 | ||||||
chr5:146483211
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2074-329C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 14/22 | chr5 | 146483211 | ||||||
chr5:146483660
|
T | TATATCTC others(4): Show |
18 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206others(15): Show | 23 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.2163+32_2163+42dup others(11): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr5 | 146483660 | |||||
chr5:146483695
|
G | A | 2 | a0001c0001t0010g0026a0001c0001t0010g0027 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.2163+66G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146483695 | ||||||
chr5:146483839
|
T | G | 1 | a0001c0001t0001g0214 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2163+210T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146483839 | ||||||
chr5:146483919
|
A | G | 4 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0229others(1): Show | 4 | NA18950.hp1 NA18978.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.2163+290A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146483919 | ||||||
chr5:146484030
|
C | A | 84 | a0001c0001t0001g0013a0001c0001t0001g0039a0001c0001t0001g0041others(81): Show | 99 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.2163+401C>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146484030 | ||||||
chr5:146484030
|
C | T | 18 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206others(15): Show | 23 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.2163+401C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146484030 | ||||||
chr5:146484514
|
A | T | 2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | HG01099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.2163+885A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146484514 | ||||||
chr5:146484520
|
A | G | 1 | a0001c0001t0002g0085 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2163+891A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146484520 | ||||||
chr5:146484581
|
G | GTA | 84 | a0001c0001t0001g0013a0001c0001t0001g0039a0001c0001t0001g0041others(81): Show | 99 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.2163+954_2163+955d others(4): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr5 | 146484581 | |||||
chr5:146484659
|
A | T | 1 | a0001c0001t0001g0033 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2163+1030A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146484659 | ||||||
chr5:146484753
|
T | G | 144 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(141): Show | 161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.2163+1124T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146484753 | ||||||
chr5:146484900
|
C | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0145 | 3 | HG00738.hp1 HG01071.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.2163+1271C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146484900 | ||||||
chr5:146484960
|
G | A | 144 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(141): Show | 161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.2163+1331G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146484960 | ||||||
chr5:146485020
|
T | C | 4 | a0002c0005t0004g0188a0002c0005t0004g0189a0002c0005t0004g0190others(1): Show | 4 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.2163+1391T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146485020 | ||||||
chr5:146485077
|
T | G | 2 | a0001c0001t0005g0018a0001c0001t0005g0199 | 3 | HG01167.hp1 HG02886.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2163+1448T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146485077 | ||||||
chr5:146485508
|
T | C | 8 | a0001c0001t0005g0017a0001c0001t0005g0018a0001c0001t0005g0194others(5): Show | 10 | HG01167.hp1 HG01884.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.2163+1879T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146485508 | ||||||
chr5:146485534
|
G | A | 1 | a0001c0001t0004g0234 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2163+1905G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146485534 | ||||||
chr5:146485549
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2163+1920C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146485549 | ||||||
chr5:146485569
|
A | G | 2 | a0001c0001t0010g0026a0001c0001t0010g0027 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.2163+1940A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146485569 | ||||||
chr5:146485701
|
C | T | 153 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(150): Show | 170 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(167): Show |
intron_variant | MODIFIER | c.2163+2072C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146485701 | ||||||
chr5:146485898
|
C | T | 270 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(267): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.2163+2269C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146485898 | ||||||
chr5:146486089
|
C | CT | 31 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(28): Show | 35 | HG00099.hp2 HG00140.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.2163+2460_2163+246 others(5): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146486089 | ||||||
chr5:146486090
|
G | T | 144 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(141): Show | 161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.2163+2461G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146486090 | ||||||
chr5:146486092
|
T | C | 19 | a0001c0001t0001g0010a0001c0001t0001g0258a0001c0001t0001g0259others(16): Show | 21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.2163+2463T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146486092 | ||||||
chr5:146486162
|
C | T | 73 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(70): Show | 91 | HG00099.hp1 HG00140.hp2 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.2163+2533C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146486162 | ||||||
chr5:146486229
|
C | T | 2 | a0002c0007t0001g0157a0002c0007t0001g0164 | 2 | HG02572.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2163+2600C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146486229 | ||||||
chr5:146486279
|
C | G | 1 | a0004c0010t0001g0236 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2163+2650C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146486279 | ||||||
chr5:146486504
|
G | T | 144 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(141): Show | 161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.2163+2875G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146486504 | ||||||
chr5:146486515
|
A | G | 1 | a0001c0001t0003g0255 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2163+2886A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146486515 | ||||||
chr5:146486575
|
C | T | 1 | a0001c0008t0009g0239 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2163+2946C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146486575 | ||||||
chr5:146486646
|
G | A | 1 | a0001c0001t0004g0234 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2163+3017G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146486646 | ||||||
chr5:146486846
|
A | G | 6 | a0001c0001t0001g0144a0001c0001t0001g0180a0003c0006t0001g0132others(3): Show | 6 | HG00733.hp2 HG01516.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.2163+3217A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146486846 | ||||||
chr5:146486895
|
C | T | 144 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(141): Show | 161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.2163+3266C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146486895 | ||||||
chr5:146486980
|
G | C | 259 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(256): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.2163+3351G>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146486980 | ||||||
chr5:146487087
|
C | CA | 152 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(149): Show | 174 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(171): Show |
intron_variant | MODIFIER | c.2163+3467dupA | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr5 | 146487087 | |||||
chr5:146487089
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2163+3460A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146487089 | ||||||
chr5:146487462
|
T | A | 3 | a0001c0003t0001g0016a0001c0003t0001g0175a0004c0021t0001g0201 | 4 | HG02615.hp1 HG02647.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2163+3833T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146487462 | ||||||
chr5:146487543
|
T | G | 1 | a0001c0001t0007g0252 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2163+3914T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146487543 | ||||||
chr5:146487592
|
A | G | 1 | a0001c0001t0002g0105 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2163+3963A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146487592 | ||||||
chr5:146487612
|
A | G | 1 | a0001c0001t0002g0105 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2163+3983A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146487612 | ||||||
chr5:146487731
|
C | CA | 24 | a0001c0001t0001g0114a0001c0001t0001g0130a0001c0001t0001g0151others(21): Show | 27 | HG01109.hp2 HG01167.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.2163+4120dupA | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr5 | 146487731 | |||||
chr5:146487731
|
CA | C | 9 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206others(6): Show | 9 | HG01934.hp1 HG02055.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2163+4120delA | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr5 | 146487731 | |||||
chr5:146487731
|
CAA | C | 7 | a0001c0001t0001g0032a0001c0001t0001g0039a0001c0001t0001g0041others(4): Show | 7 | HG01243.hp2 HG02109.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2163+4119_2163+412 others(6): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr5 | 146487731 | |||||
chr5:146487731
|
CAAA | C | 136 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(133): Show | 153 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(150): Show |
intron_variant | MODIFIER | c.2163+4118_2163+412 others(7): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr5 | 146487731 | |||||
chr5:146487751
|
C | G | 1 | a0001c0001t0008g0028 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2163+4122C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146487751 | ||||||
chr5:146487754
|
A | G | 144 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(141): Show | 161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.2163+4125A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146487754 | ||||||
chr5:146487867
|
TAACTAA | T | 5 | a0001c0001t0005g0017a0001c0001t0005g0194a0001c0001t0005g0195others(2): Show | 6 | HG01884.hp1 HG02486.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2163+4242_2163+424 others(10): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr5 | 146487867 | |||||
chr5:146487881
|
C | T | 241 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(238): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.2163+4252C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146487881 | ||||||
chr5:146487898
|
C | T | 1 | a0001c0001t0007g0252 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2163+4269C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146487898 | ||||||
chr5:146487971
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2163+4342A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146487971 | ||||||
chr5:146488012
|
T | A | 1 | a0003c0019t0001g0235 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2163+4383T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146488012 | ||||||
chr5:146488045
|
A | G | 1 | a0001c0001t0004g0112 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2163+4416A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146488045 | ||||||
chr5:146488111
|
C | G | 1 | a0001c0001t0001g0159 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2163+4482C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146488111 | ||||||
chr5:146488260
|
A | T | 8 | a0001c0001t0005g0017a0001c0001t0005g0018a0001c0001t0005g0194others(5): Show | 10 | HG01167.hp1 HG01884.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.2163+4631A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146488260 | ||||||
chr5:146488335
|
T | C | 1 | a0001c0001t0002g0090 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2164-4585T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146488335 | ||||||
chr5:146488858
|
T | C | 2 | a0002c0007t0001g0157a0002c0007t0001g0164 | 2 | HG02572.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2164-4062T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146488858 | ||||||
chr5:146489104
|
T | G | 1 | a0001c0001t0002g0091 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2164-3816T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146489104 | ||||||
chr5:146489127
|
C | G | 144 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(141): Show | 161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.2164-3793C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146489127 | ||||||
chr5:146489128
|
G | A | 9 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206others(6): Show | 9 | HG01934.hp1 HG02055.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2164-3792G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146489128 | ||||||
chr5:146489327
|
A | G | 3 | a0001c0001t0001g0225a0001c0001t0001g0226a0004c0010t0001g0236 | 3 | HG02451.hp2 HG03209.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2164-3593A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146489327 | ||||||
chr5:146489550
|
T | C | 1 | a0001c0001t0001g0127 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2164-3370T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146489550 | ||||||
chr5:146489632
|
A | G | 36 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(33): Show | 36 | HG00738.hp2 HG01257.hp2 HG01258.hp1 others(33): Show |
intron_variant | MODIFIER | c.2164-3288A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146489632 | ||||||
chr5:146489789
|
A | G | 1 | a0001c0001t0001g0155 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2164-3131A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146489789 | ||||||
chr5:146489865
|
A | G | 144 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(141): Show | 161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.2164-3055A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146489865 | ||||||
chr5:146490041
|
G | A | 1 | a0001c0018t0002g0070 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2164-2879G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146490041 | ||||||
chr5:146490152
|
A | C | 124 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0031others(121): Show | 139 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(136): Show |
intron_variant | MODIFIER | c.2164-2768A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146490152 | ||||||
chr5:146490183
|
G | C | 19 | a0001c0001t0001g0010a0001c0001t0001g0258a0001c0001t0001g0259others(16): Show | 21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.2164-2737G>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146490183 | ||||||
chr5:146490257
|
A | C | 266 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(263): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.2164-2663A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146490257 | ||||||
chr5:146490409
|
T | C | 1 | a0001c0001t0002g0092 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2164-2511T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146490409 | ||||||
chr5:146490516
|
C | T | 1 | a0001c0001t0004g0234 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2164-2404C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146490516 | ||||||
chr5:146490517
|
G | A | 84 | a0001c0001t0001g0013a0001c0001t0001g0039a0001c0001t0001g0041others(81): Show | 99 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.2164-2403G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146490517 | ||||||
chr5:146490755
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2164-2165T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146490755 | ||||||
chr5:146490846
|
T | C | 1 | a0001c0001t0007g0020 | 2 | HG02622.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2164-2074T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146490846 | ||||||
chr5:146490976
|
T | C | 1 | a0001c0001t0001g0207 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2164-1944T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146490976 | ||||||
chr5:146491014
|
T | G | 19 | a0001c0001t0001g0010a0001c0001t0001g0258a0001c0001t0001g0259others(16): Show | 21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.2164-1906T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146491014 | ||||||
chr5:146491188
|
C | T | 1 | a0001c0001t0006g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2164-1732C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146491188 | ||||||
chr5:146491318
|
C | T | 11 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(8): Show | 11 | HG00738.hp2 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.2164-1602C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146491318 | ||||||
chr5:146491511
|
G | A | 31 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(28): Show | 35 | HG00099.hp2 HG00140.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.2164-1409G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146491511 | ||||||
chr5:146491535
|
A | T | 144 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(141): Show | 161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.2164-1385A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146491535 | ||||||
chr5:146491628
|
C | G | 75 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(72): Show | 93 | HG00099.hp1 HG00140.hp2 HG00621.hp2 others(90): Show |
intron_variant | MODIFIER | c.2164-1292C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146491628 | ||||||
chr5:146491765
|
A | G | 144 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(141): Show | 161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.2164-1155A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146491765 | ||||||
chr5:146491766
|
T | A | 87 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(84): Show | 106 | HG00099.hp1 HG00140.hp2 HG00621.hp2 others(103): Show |
intron_variant | MODIFIER | c.2164-1154T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146491766 | ||||||
chr5:146491800
|
C | T | 2 | a0001c0001t0010g0026a0001c0001t0010g0027 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.2164-1120C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146491800 | ||||||
chr5:146491960
|
A | AC | 144 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(141): Show | 161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.2164-958dupC | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr5 | 146491960 | |||||
chr5:146492021
|
T | G | 1 | a0001c0001t0005g0194 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2164-899T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146492021 | ||||||
chr5:146492527
|
G | A | 3 | a0001c0002t0003g0005a0001c0002t0003g0242a0001c0002t0003g0243 | 6 | HG01261.hp2 HG01361.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2164-393G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146492527 | ||||||
chr5:146492542
|
C | T | 2 | a0001c0001t0010g0026a0001c0001t0010g0027 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.2164-378C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146492542 | ||||||
chr5:146492555
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2164-365T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146492555 | ||||||
chr5:146492710
|
G | C | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2164-210G>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146492710 | ||||||
chr5:146492818
|
T | A | 19 | a0001c0001t0001g0010a0001c0001t0001g0258a0001c0001t0001g0259others(16): Show | 21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.2164-102T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146492818 | ||||||
chr5:146492888
|
T | G | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG02080.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.2164-32T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146492888 | ||||||
chr5:146493274
|
T | C | 3 | a0001c0001t0002g0043a0001c0001t0002g0086a0001c0001t0002g0093 | 3 | HG03491.hp1 NA18952.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.2282+236T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146493274 | ||||||
chr5:146493288
|
T | C | 1 | a0001c0001t0002g0105 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2282+250T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146493288 | ||||||
chr5:146493311
|
C | T | 1 | a0001c0001t0010g0026 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2282+273C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146493311 | ||||||
chr5:146493324
|
T | C | 1 | a0001c0001t0004g0234 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2282+286T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146493324 | ||||||
chr5:146493355
|
A | G | 4 | a0002c0005t0004g0188a0002c0005t0004g0189a0002c0005t0004g0190others(1): Show | 4 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.2282+317A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146493355 | ||||||
chr5:146493700
|
C | G | 8 | a0001c0002t0003g0005a0001c0002t0003g0009a0001c0002t0003g0240others(5): Show | 13 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.2282+662C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146493700 | ||||||
chr5:146493802
|
T | C | 143 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(140): Show | 160 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.2282+764T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146493802 | ||||||
chr5:146493968
|
G | A | 1 | a0001c0001t0001g0210 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2282+930G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146493968 | ||||||
chr5:146493971
|
A | T | 19 | a0001c0001t0001g0010a0001c0001t0001g0258a0001c0001t0001g0259others(16): Show | 21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.2282+933A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146493971 | ||||||
chr5:146494048
|
A | G | 4 | a0001c0001t0002g0090a0001c0001t0002g0095a0001c0001t0002g0096others(1): Show | 4 | NA18954.hp2 NA19054.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.2282+1010A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146494048 | ||||||
chr5:146494389
|
G | A | 1 | a0001c0001t0004g0234 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2282+1351G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146494389 | ||||||
chr5:146494475
|
C | A | 3 | a0001c0001t0003g0255a0001c0001t0003g0256a0001c0001t0003g0257 | 3 | HG02970.hp1 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2282+1437C>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146494475 | ||||||
chr5:146494718
|
AGTAGAGC others(14): Show |
A | 1 | a0001c0001t0002g0087 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2282+1681_2282+170 others(25): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146494718 | ||||||
chr5:146494852
|
T | C | 1 | a0001c0001t0001g0134 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2282+1814T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146494852 | ||||||
chr5:146494863
|
T | C | 86 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(83): Show | 105 | HG00099.hp1 HG00140.hp2 HG00621.hp2 others(102): Show |
intron_variant | MODIFIER | c.2282+1825T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146494863 | ||||||
chr5:146495188
|
T | G | 1 | a0001c0001t0002g0087 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2282+2150T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146495188 | ||||||
chr5:146495222
|
T | A | 1 | a0001c0001t0001g0212 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2282+2184T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146495222 | ||||||
chr5:146495498
|
T | C | 1 | a0001c0001t0005g0017 | 2 | HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2282+2460T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146495498 | ||||||
chr5:146495534
|
A | G | 145 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(142): Show | 162 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(159): Show |
intron_variant | MODIFIER | c.2282+2496A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146495534 | ||||||
chr5:146495605
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2282+2567A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146495605 | ||||||
chr5:146495696
|
T | G | 18 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206others(15): Show | 23 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.2282+2658T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146495696 | ||||||
chr5:146495739
|
CTTTGT | C | 36 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(33): Show | 36 | HG00738.hp2 HG01257.hp2 HG01258.hp1 others(33): Show |
intron_variant | MODIFIER | c.2282+2705_2282+270 others(9): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr5 | 146495739 | |||||
chr5:146495880
|
C | T | 1 | a0001c0001t0001g0230 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2283-2656C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146495880 | ||||||
chr5:146495907
|
C | G | 10 | a0001c0001t0007g0020a0001c0002t0003g0005a0001c0002t0003g0009others(7): Show | 16 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.2283-2629C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146495907 | ||||||
chr5:146496007
|
G | T | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2283-2529G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146496007 | ||||||
chr5:146496077
|
T | C | 3 | a0001c0001t0003g0255a0001c0001t0003g0256a0001c0001t0003g0257 | 3 | HG02970.hp1 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2283-2459T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146496077 | ||||||
chr5:146496107
|
G | A | 1 | a0001c0001t0005g0198 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2283-2429G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146496107 | ||||||
chr5:146496129
|
A | G | 3 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0247 | 3 | NA19002.hp1 NA19074.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.2283-2407A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146496129 | ||||||
chr5:146496235
|
T | A | 1 | a0001c0001t0002g0087 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2283-2301T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146496235 | ||||||
chr5:146496507
|
A | C | 3 | a0005c0014t0004g0185a0006c0009t0004g0186a0006c0009t0004g0187 | 3 | HG01496.hp2 HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2283-2029A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146496507 | ||||||
chr5:146496558
|
T | C | 124 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0031others(121): Show | 139 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(136): Show |
intron_variant | MODIFIER | c.2283-1978T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146496558 | ||||||
chr5:146496563
|
A | T | 1 | a0001c0001t0002g0087 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2283-1973A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146496563 | ||||||
chr5:146496869
|
G | GT | 11 | a0001c0001t0001g0118a0001c0001t0001g0128a0001c0001t0005g0018others(8): Show | 12 | HG00673.hp1 HG01167.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.2283-1645dupT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr5 | 146496869 | |||||
chr5:146496869
|
GT | G | 80 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(77): Show | 99 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(96): Show |
intron_variant | MODIFIER | c.2283-1645delT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr5 | 146496869 | |||||
chr5:146496869
|
GTT | G | 37 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(34): Show | 37 | HG00738.hp2 HG01257.hp2 HG01258.hp1 others(34): Show |
intron_variant | MODIFIER | c.2283-1646_2283-164 others(6): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr5 | 146496869 | |||||
chr5:146496869
|
GTTT | G | 102 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(99): Show | 119 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(116): Show |
intron_variant | MODIFIER | c.2283-1647_2283-164 others(7): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr5 | 146496869 | |||||
chr5:146496877
|
T | G | 1 | a0001c0001t0004g0112 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2283-1659T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146496877 | ||||||
chr5:146496915
|
C | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0142 | 3 | HG01346.hp2 HG01496.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.2283-1621C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146496915 | ||||||
chr5:146496936
|
T | G | 1 | a0001c0001t0004g0234 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2283-1600T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146496936 | ||||||
chr5:146496994
|
A | T | 1 | a0001c0002t0003g0243 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2283-1542A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146496994 | ||||||
chr5:146497023
|
A | T | 1 | a0001c0001t0002g0087 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2283-1513A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146497023 | ||||||
chr5:146497111
|
A | G | 85 | a0001c0001t0001g0013a0001c0001t0001g0039a0001c0001t0001g0041others(82): Show | 100 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.2283-1425A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146497111 | ||||||
chr5:146497297
|
A | T | 1 | a0001c0001t0002g0087 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2283-1239A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146497297 | ||||||
chr5:146497325
|
T | C | 145 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(142): Show | 162 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(159): Show |
intron_variant | MODIFIER | c.2283-1211T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146497325 | ||||||
chr5:146497372
|
C | T | 1 | a0001c0001t0002g0087 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2283-1164C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146497372 | ||||||
chr5:146497374
|
T | C | 1 | a0001c0001t0002g0087 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2283-1162T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146497374 | ||||||
chr5:146497375
|
G | T | 1 | a0001c0001t0002g0087 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2283-1161G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146497375 | ||||||
chr5:146497397
|
T | A | 1 | a0001c0001t0002g0087 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2283-1139T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146497397 | ||||||
chr5:146497409
|
C | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(71): Show | 92 | HG00099.hp1 HG00140.hp2 HG00621.hp2 others(89): Show |
intron_variant | MODIFIER | c.2283-1127C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146497409 | ||||||
chr5:146497584
|
A | G | 1 | a0001c0015t0002g0103 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2283-952A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146497584 | ||||||
chr5:146497600
|
A | G | 1 | a0001c0001t0001g0216 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2283-936A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146497600 | ||||||
chr5:146497689
|
T | C | 6 | a0002c0005t0004g0188a0002c0005t0004g0189a0002c0005t0004g0190others(3): Show | 6 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.2283-847T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146497689 | ||||||
chr5:146497826
|
C | T | 1 | a0001c0001t0003g0254 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2283-710C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146497826 | ||||||
chr5:146497837
|
C | A | 1 | a0001c0001t0008g0029 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2283-699C>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146497837 | ||||||
chr5:146497934
|
G | A | 24 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(21): Show | 24 | HG01257.hp2 HG01258.hp1 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.2283-602G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146497934 | ||||||
chr5:146497951
|
T | C | 1 | a0001c0001t0001g0032 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2283-585T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146497951 | ||||||
chr5:146498005
|
C | G | 9 | a0001c0002t0003g0005a0001c0002t0003g0009a0001c0002t0003g0113others(6): Show | 14 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.2283-531C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146498005 | ||||||
chr5:146498089
|
G | A | 3 | a0005c0014t0004g0185a0006c0009t0004g0186a0006c0009t0004g0187 | 3 | HG01496.hp2 HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2283-447G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146498089 | ||||||
chr5:146498094
|
AC | A | 6 | a0002c0005t0004g0188a0002c0005t0004g0189a0002c0005t0004g0190others(3): Show | 6 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.2283-441delC | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146498094 | ||||||
chr5:146498110
|
A | G | 2 | a0001c0001t0003g0205a0001c0001t0003g0206 | 2 | HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2283-426A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146498110 | ||||||
chr5:146498311
|
T | A | 19 | a0001c0001t0001g0010a0001c0001t0001g0258a0001c0001t0001g0259others(16): Show | 21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.2283-225T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146498311 | ||||||
chr5:146498523
|
A | G | 2 | a0001c0001t0010g0026a0001c0001t0010g0027 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.2283-13A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146498523 | ||||||
chr5:146498524
|
A | T | 1 | a0001c0001t0002g0087 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2283-12A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146498524 | ||||||
chr5:146498764
|
A | C | 1 | a0001c0001t0001g0141 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2433+78A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146498764 | ||||||
chr5:146498809
|
T | A | 1 | a0001c0001t0002g0087 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2433+123T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146498809 | ||||||
chr5:146499150
|
T | A | 1 | a0001c0001t0002g0087 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2433+464T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146499150 | ||||||
chr5:146499186
|
G | A | 1 | a0001c0001t0002g0065 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2433+500G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146499186 | ||||||
chr5:146499187
|
A | C | 2 | a0001c0004t0004g0249a0001c0004t0004g0250 | 2 | HG01346.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.2433+501A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146499187 | ||||||
chr5:146499449
|
T | A | 1 | a0001c0001t0002g0087 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2433+763T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146499449 | ||||||
chr5:146499647
|
A | G | 1 | a0008c0017t0002g0036 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2433+961A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146499647 | ||||||
chr5:146499750
|
A | C | 163 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(160): Show | 185 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(182): Show |
intron_variant | MODIFIER | c.2433+1064A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146499750 | ||||||
chr5:146500103
|
C | T | 3 | a0001c0001t0003g0255a0001c0001t0003g0256a0001c0001t0003g0257 | 3 | HG02970.hp1 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2433+1417C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146500103 | ||||||
chr5:146500262
|
C | G | 1 | a0001c0001t0002g0085 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2433+1576C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146500262 | ||||||
chr5:146500319
|
A | C | 1 | a0001c0001t0001g0129 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2433+1633A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146500319 | ||||||
chr5:146500403
|
TA | T | 87 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(84): Show | 107 | HG00099.hp1 HG00140.hp2 HG00673.hp1 others(104): Show |
intron_variant | MODIFIER | c.2433+1729delA | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 146500403 | |||||
chr5:146500403
|
TAA | T | 163 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(160): Show | 185 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(182): Show |
intron_variant | MODIFIER | c.2433+1728_2433+172 others(6): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 146500403 | |||||
chr5:146500469
|
G | A | 1 | a0001c0001t0002g0105 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2433+1783G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146500469 | ||||||
chr5:146500514
|
A | C | 1 | a0001c0001t0007g0252 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2433+1828A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146500514 | ||||||
chr5:146500866
|
G | A | 1 | a0001c0001t0001g0273 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2433+2180G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146500866 | ||||||
chr5:146500891
|
C | G | 1 | a0001c0001t0001g0229 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2433+2205C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146500891 | ||||||
chr5:146500962
|
G | A | 2 | a0001c0008t0009g0238a0001c0008t0009g0239 | 2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2433+2276G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146500962 | ||||||
chr5:146501004
|
C | CA | 10 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206others(7): Show | 10 | HG01934.hp1 HG02055.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.2433+2333dupA | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 146501004 | |||||
chr5:146501004
|
CA | C | 241 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(238): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.2433+2333delA | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 146501004 | |||||
chr5:146501004
|
CAA | C | 6 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(3): Show | 6 | HG01099.hp2 HG01168.hp2 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.2433+2332_2433+233 others(6): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 146501004 | |||||
chr5:146501149
|
A | T | 8 | a0001c0001t0005g0017a0001c0001t0005g0018a0001c0001t0005g0194others(5): Show | 10 | HG01167.hp1 HG01884.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.2434-2226A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146501149 | ||||||
chr5:146501288
|
A | G | 1 | a0001c0001t0001g0138 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2434-2087A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146501288 | ||||||
chr5:146501346
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2434-2029G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146501346 | ||||||
chr5:146501346
|
G | GAT | 163 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(160): Show | 185 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(182): Show |
intron_variant | MODIFIER | c.2434-2027_2434-202 others(6): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 146501346 | |||||
chr5:146501633
|
G | T | 2 | a0001c0001t0002g0003a0001c0001t0002g0108 | 5 | HG01256.hp1 HG01258.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.2434-1742G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146501633 | ||||||
chr5:146501688
|
C | T | 18 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206others(15): Show | 23 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.2434-1687C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146501688 | ||||||
chr5:146501887
|
C | CT | 39 | a0001c0001t0001g0013a0001c0001t0001g0048a0001c0001t0001g0208others(36): Show | 40 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.2434-1462dupT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 146501887 | |||||
chr5:146501887
|
CT | C | 27 | a0001c0001t0001g0010a0001c0001t0001g0150a0001c0001t0001g0258others(24): Show | 29 | HG01934.hp1 HG01943.hp1 HG02080.hp1 others(26): Show |
intron_variant | MODIFIER | c.2434-1462delT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 146501887 | |||||
chr5:146501887
|
CTT | C | 10 | a0001c0001t0001g0116a0001c0001t0001g0119a0001c0001t0001g0137others(7): Show | 10 | HG01069.hp2 HG01891.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.2434-1463_2434-146 others(6): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 146501887 | |||||
chr5:146501887
|
CTTT | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(74): Show | 97 | HG00099.hp1 HG00140.hp2 HG00621.hp2 others(94): Show |
intron_variant | MODIFIER | c.2434-1464_2434-146 others(7): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 146501887 | |||||
chr5:146501887
|
CTTTTTTT others(6): Show |
C | 3 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG01243.hp2 HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2434-1474_2434-146 others(17): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 146501887 | |||||
chr5:146501915
|
A | T | 1 | a0001c0001t0005g0195 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2434-1460A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146501915 | ||||||
chr5:146501924
|
TTTGC | T | 9 | a0001c0002t0003g0005a0001c0002t0003g0009a0001c0002t0003g0113others(6): Show | 14 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.2434-1447_2434-144 others(8): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 146501924 | |||||
chr5:146501974
|
C | A | 145 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(142): Show | 162 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(159): Show |
intron_variant | MODIFIER | c.2434-1401C>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146501974 | ||||||
chr5:146502031
|
T | A | 164 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(161): Show | 186 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(183): Show |
intron_variant | MODIFIER | c.2434-1344T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146502031 | ||||||
chr5:146502228
|
G | A | 88 | a0001c0001t0001g0013a0001c0001t0001g0039a0001c0001t0001g0041others(85): Show | 103 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.2434-1147G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146502228 | ||||||
chr5:146502420
|
G | T | 4 | a0002c0005t0004g0188a0002c0005t0004g0189a0002c0005t0004g0190others(1): Show | 4 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.2434-955G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146502420 | ||||||
chr5:146502742
|
G | A | 19 | a0001c0001t0001g0010a0001c0001t0001g0258a0001c0001t0001g0259others(16): Show | 21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.2434-633G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146502742 | ||||||
chr5:146502974
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2434-401A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146502974 | ||||||
chr5:146503230
|
A | C | 1 | a0001c0001t0001g0035 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2434-145A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146503230 | ||||||
chr5:146503571
|
T | C | 1 | a0001c0002t0003g0243 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2598+32T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 18/22 | chr5 | 146503571 | ||||||
chr5:146503800
|
A | G | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | HG02056.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.2599-24A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 18/22 | chr5 | 146503800 | ||||||
chr5:146504054
|
A | C | 2 | a0001c0001t0010g0026a0001c0001t0010g0027 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.2781+48A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146504054 | ||||||
chr5:146504326
|
G | A | 84 | a0001c0001t0001g0013a0001c0001t0001g0039a0001c0001t0001g0041others(81): Show | 99 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.2781+320G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146504326 | ||||||
chr5:146504341
|
T | C | 1 | a0001c0001t0007g0252 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2781+335T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146504341 | ||||||
chr5:146504350
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2781+344C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146504350 | ||||||
chr5:146504866
|
G | A | 1 | a0001c0001t0013g0203 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2781+860G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146504866 | ||||||
chr5:146504884
|
T | C | 1 | a0001c0001t0002g0045 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2781+878T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146504884 | ||||||
chr5:146504903
|
G | A | 19 | a0001c0001t0001g0010a0001c0001t0001g0258a0001c0001t0001g0259others(16): Show | 21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.2781+897G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146504903 | ||||||
chr5:146504913
|
G | T | 2 | a0001c0001t0010g0026a0001c0001t0010g0027 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.2781+907G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146504913 | ||||||
chr5:146504917
|
G | C | 1 | a0001c0001t0001g0274 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2781+911G>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146504917 | ||||||
chr5:146504968
|
C | T | 8 | a0001c0002t0003g0005a0001c0002t0003g0009a0001c0002t0003g0240others(5): Show | 13 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.2781+962C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146504968 | ||||||
chr5:146504987
|
C | A | 154 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(151): Show | 171 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(168): Show |
intron_variant | MODIFIER | c.2781+981C>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146504987 | ||||||
chr5:146505052
|
A | G | 1 | a0001c0001t0003g0204 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2781+1046A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146505052 | ||||||
chr5:146505087
|
T | TA | 19 | a0001c0001t0001g0130a0001c0001t0001g0161a0001c0001t0004g0112others(16): Show | 25 | HG00733.hp1 HG01109.hp2 HG01256.hp2 others(22): Show |
intron_variant | MODIFIER | c.2781+1099dupA | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr5 | 146505087 | |||||
chr5:146505087
|
TA | T | 136 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0039others(133): Show | 155 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(152): Show |
intron_variant | MODIFIER | c.2781+1099delA | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr5 | 146505087 | |||||
chr5:146505087
|
TAA | T | 10 | a0001c0001t0003g0204a0001c0001t0003g0206a0001c0001t0003g0254others(7): Show | 10 | HG01934.hp1 HG02055.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.2781+1098_2781+109 others(6): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr5 | 146505087 | |||||
chr5:146505118
|
C | T | 1 | a0001c0001t0004g0112 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2781+1112C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146505118 | ||||||
chr5:146505231
|
C | T | 1 | a0001c0001t0002g0061 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2781+1225C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146505231 | ||||||
chr5:146505258
|
C | G | 2 | a0001c0001t0002g0078a0001c0001t0002g0079 | 2 | HG02040.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.2781+1252C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146505258 | ||||||
chr5:146505288
|
C | T | 1 | a0001c0001t0010g0026 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2781+1282C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146505288 | ||||||
chr5:146505294
|
G | A | 154 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(151): Show | 171 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(168): Show |
intron_variant | MODIFIER | c.2781+1288G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146505294 | ||||||
chr5:146505322
|
G | C | 1 | a0001c0001t0001g0220 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2781+1316G>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146505322 | ||||||
chr5:146505391
|
C | A | 4 | a0001c0001t0006g0022a0001c0001t0006g0023a0001c0001t0006g0024others(1): Show | 4 | HG02559.hp2 HG02572.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2781+1385C>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146505391 | ||||||
chr5:146505485
|
C | A | 19 | a0001c0001t0001g0010a0001c0001t0001g0258a0001c0001t0001g0259others(16): Show | 21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.2781+1479C>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146505485 | ||||||
chr5:146505486
|
A | AT | 259 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(256): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.2781+1482dupT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr5 | 146505486 | |||||
chr5:146505490
|
T | C | 154 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(151): Show | 171 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(168): Show |
intron_variant | MODIFIER | c.2781+1484T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146505490 | ||||||
chr5:146505622
|
G | GT | 8 | a0001c0002t0003g0005a0001c0002t0003g0009a0001c0002t0003g0240others(5): Show | 13 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.2782-1405dupT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr5 | 146505622 | |||||
chr5:146505626
|
G | A | 3 | a0001c0002t0003g0005a0001c0002t0003g0242a0001c0002t0003g0243 | 6 | HG01261.hp2 HG01361.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2782-1402G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146505626 | ||||||
chr5:146505651
|
A | G | 1 | a0001c0001t0002g0088 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2782-1377A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146505651 | ||||||
chr5:146505708
|
C | T | 10 | a0001c0001t0007g0020a0001c0002t0003g0005a0001c0002t0003g0009others(7): Show | 16 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.2782-1320C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146505708 | ||||||
chr5:146505717
|
A | ACT | 154 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(151): Show | 171 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(168): Show |
intron_variant | MODIFIER | c.2782-1310_2782-130 others(6): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr5 | 146505717 | |||||
chr5:146505758
|
A | G | 2 | a0001c0001t0010g0026a0001c0001t0010g0027 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.2782-1270A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146505758 | ||||||
chr5:146505808
|
C | T | 1 | a0001c0004t0004g0248 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2782-1220C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146505808 | ||||||
chr5:146505886
|
C | T | 123 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0031others(120): Show | 138 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(135): Show |
intron_variant | MODIFIER | c.2782-1142C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146505886 | ||||||
chr5:146505934
|
A | T | 1 | a0001c0001t0005g0198 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2782-1094A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146505934 | ||||||
chr5:146506035
|
G | A | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2782-993G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146506035 | ||||||
chr5:146506061
|
G | A | 24 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(21): Show | 24 | HG01257.hp2 HG01258.hp1 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.2782-967G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146506061 | ||||||
chr5:146506120
|
A | G | 153 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(150): Show | 170 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(167): Show |
intron_variant | MODIFIER | c.2782-908A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146506120 | ||||||
chr5:146506202
|
A | T | 1 | a0001c0001t0001g0168 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2782-826A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146506202 | ||||||
chr5:146506218
|
G | C | 154 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(151): Show | 171 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(168): Show |
intron_variant | MODIFIER | c.2782-810G>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146506218 | ||||||
chr5:146506321
|
G | A | 9 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206others(6): Show | 9 | HG01934.hp1 HG02055.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2782-707G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146506321 | ||||||
chr5:146506368
|
C | T | 1 | a0001c0001t0004g0234 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2782-660C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146506368 | ||||||
chr5:146506400
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2782-628G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146506400 | ||||||
chr5:146506467
|
C | G | 1 | a0001c0001t0002g0071 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2782-561C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146506467 | ||||||
chr5:146506475
|
C | T | 1 | a0001c0016t0001g0136 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2782-553C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146506475 | ||||||
chr5:146507273
|
G | A | 3 | a0003c0006t0001g0132a0003c0006t0001g0133a0003c0006t0001g0171 | 3 | HG00733.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2961+66G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 20/22 | chr5 | 146507273 | ||||||
chr5:146507279
|
A | G | 8 | a0001c0001t0005g0017a0001c0001t0005g0018a0001c0001t0005g0194others(5): Show | 10 | HG01167.hp1 HG01884.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.2961+72A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 20/22 | chr5 | 146507279 | ||||||
chr5:146507357
|
TG | T | 8 | a0001c0001t0005g0017a0001c0001t0005g0018a0001c0001t0005g0194others(5): Show | 10 | HG01167.hp1 HG01884.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.2961+152delG | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | 146507357 | |||||
chr5:146507381
|
G | A | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | HG02056.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.2961+174G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 20/22 | chr5 | 146507381 | ||||||
chr5:146507394
|
A | G | 19 | a0001c0001t0001g0010a0001c0001t0001g0258a0001c0001t0001g0259others(16): Show | 21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.2961+187A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 20/22 | chr5 | 146507394 | ||||||
chr5:146507532
|
C | T | 1 | a0003c0019t0001g0235 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2961+325C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 20/22 | chr5 | 146507532 | ||||||
chr5:146507573
|
T | C | 164 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(161): Show | 186 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(183): Show |
intron_variant | MODIFIER | c.2962-300T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 20/22 | chr5 | 146507573 | ||||||
chr5:146508325
|
C | T | 9 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206others(6): Show | 9 | HG01934.hp1 HG02055.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.3045+369C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 21/22 | chr5 | 146508325 | ||||||
chr5:146508336
|
A | G | 86 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(83): Show | 105 | HG00099.hp1 HG00140.hp2 HG00621.hp2 others(102): Show |
intron_variant | MODIFIER | c.3045+380A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 21/22 | chr5 | 146508336 | ||||||
chr5:146508521
|
T | C | 1 | a0001c0001t0002g0083 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.3045+565T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 21/22 | chr5 | 146508521 | ||||||
chr5:146508748
|
C | G | 145 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(142): Show | 162 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(159): Show |
intron_variant | MODIFIER | c.3046-397C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 21/22 | chr5 | 146508748 | ||||||
chr5:146508752
|
T | C | 8 | a0001c0002t0003g0005a0001c0002t0003g0009a0001c0002t0003g0240others(5): Show | 13 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.3046-393T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 21/22 | chr5 | 146508752 | ||||||
chr5:146509046
|
A | G | 1 | a0001c0001t0001g0223 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.3046-99A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 21/22 | chr5 | 146509046 | ||||||
chr5:146509412
|
C | CT | 63 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(60): Show | 67 | HG00738.hp2 HG01243.hp2 HG01257.hp2 others(64): Show |
intron_variant | MODIFIER | c.3146+181dupT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr5 | 146509412 | |||||
chr5:146509412
|
CT | C | 7 | a0001c0001t0001g0014a0001c0001t0001g0142a0001c0001t0001g0145others(4): Show | 8 | HG00673.hp2 HG01346.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.3146+181delT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr5 | 146509412 | |||||
chr5:146509426
|
T | TA | 3 | a0001c0001t0002g0037a0001c0001t0002g0104a0001c0015t0002g0103 | 3 | HG02027.hp2 NA18942.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.3146+184dupA | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr5 | 146509426 | |||||
chr5:146509492
|
CT | C | 143 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0030others(140): Show | 161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.3146+261delT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr5 | 146509492 | |||||
chr5:146509560
|
G | C | 80 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0006others(77): Show | 94 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.3146+315G>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 22/22 | chr5 | 146509560 | ||||||
chr5:146509672
|
A | G | 85 | a0001c0001t0001g0013a0001c0001t0001g0039a0001c0001t0001g0041others(82): Show | 100 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.3146+427A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 22/22 | chr5 | 146509672 | ||||||
chr5:146509676
|
A | AT | 13 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(10): Show | 13 | HG00738.hp2 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.3146+440dupT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr5 | 146509676 | |||||
chr5:146509714
|
C | T | 2 | a0001c0001t0003g0205a0001c0001t0003g0206 | 2 | HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3146+469C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 22/22 | chr5 | 146509714 | ||||||
chr5:146510318
|
T | TA | 7 | a0001c0001t0001g0015a0001c0001t0001g0145a0001c0001t0005g0017others(4): Show | 9 | HG00738.hp1 HG01071.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.3147-100dupA | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr5 | 146510318 | |||||
chr5:146510318
|
TA | T | 130 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0039others(127): Show | 147 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(144): Show |
intron_variant | MODIFIER | c.3147-100delA | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr5 | 146510318 | |||||
chr5:146510318
|
TAA | T | 16 | a0001c0001t0001g0211a0001c0001t0001g0218a0001c0001t0001g0225others(13): Show | 16 | HG01257.hp2 HG02451.hp2 HG02523.hp2 others(13): Show |
intron_variant | MODIFIER | c.3147-101_3147-100d others(4): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr5 | 146510318 |